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_CP009279	Paenibacillus sp. FSL H7-0737, complete genome	11 crisprs	csa3,WYL,DEDDh,DinG,cas3,casR	1	4	9	0

1. NZ_CP009279

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP009279_1

• CRISPR_ID: NZ_CP009279_1
• CRISPR_location: 553530-553716
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP009279_1

Consensus_repeat	Method
TTAGAGGGAGGAATTCCCTATAA	CRISPRCasFinder

spacers of NZ_CP009279_1

>1.1|553553|28|NZ_CP009279|CRISPRCasFinder
TTCCGAGCTTAAGTGACTTTCGATCTTG
>1.2|553604|39|NZ_CP009279|CRISPRCasFinder
ATTGGCTGATTGGTCTATAAACCATGCGAATTTAGGTTT
>1.3|553666|28|NZ_CP009279|CRISPRCasFinder
TCGTGGAATTCAAGTGATTATTAGCTAA

CRISPR arrays and Neighbor proteins around NZ_CP009279_1

CRISPR arrays

The CRISPR arrays of NZ_CP009279_1

>merge|NZ_CP009279|1|553530-553716|CRISPRCasFinder
TTATAGGGAAAAACTCCCTATATTTCCGAGCTTAAGTGACTTTCGATCTTGTTATAGGGAAAGTCTCCCTCTAAATTGGCTGATTGGTCTATAAACCATGCGAATTTAGGTTTTTAGAGGGAGGAATTCCCTATAATCGTGGAATTCAAGTGATTATTAGCTAATTAGAGGGAGGAATTCCCTATAT

>NZ_CP009279|1|1|553530-553716|CRISPRCasFinder
TTATAGGGAAAAACTCCCTATAT	TTCCGAGCTTAAGTGACTTTCGATCTTG
TTATAGGGAAAGTCTCCCTCTAA	ATTGGCTGATTGGTCTATAAACCATGCGAATTTAGGTTT
TTAGAGGGAGGAATTCCCTATAA	TCGTGGAATTCAAGTGATTATTAGCTAA
TTAGAGGGAGGAATTCCCTATAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042184515.1|559189_560602_+|two-component-sensor-histidine-kinase	unknown	unknown	gnl|CDD|236848
NZ_CP009279.1|WP_042184509.1|555549_557430_-|DoxX-family-membrane-protein	unknown	unknown	gnl|CDD|224172
NZ_CP009279.1|WP_042184507.1|554855_555305_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_052404135.1|546376_547231_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|275313
NZ_CP009279.1|WP_042184511.1|557478_558369_-|hypothetical-protein	unknown	unknown	gnl|CDD|227275
NZ_CP009279.1|WP_042184519.1|563216_563993_-|tryptophan-rich-sensory-protein	unknown	unknown	gnl|CDD|376985
NZ_CP009279.1|WP_042123757.1|545789_546347_+|Gx-transporter-family-protein	unknown	unknown	gnl|CDD|377839
NZ_CP009279.1|WP_042184501.1|550977_552264_+|aspartate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|99735
NZ_CP009279.1|WP_042184517.1|562751_563132_+|RidA-family-protein	unknown	unknown	gnl|CDD|129116
NZ_CP009279.1|WP_042184499.1|548954_550880_+|peptidase-U32	unknown	unknown	gnl|CDD|223896
NZ_CP009279.1|WP_042184491.1|543750_544686_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223999
NZ_CP009279.1|WP_042184497.1|548119_548911_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	unknown	unknown	gnl|CDD|223692
NZ_CP009279.1|WP_042184495.1|547221_548127_+|energy-coupling-factor-transporter-ATPase	unknown	unknown	gnl|CDD|275314
NZ_CP009279.1|WP_042184503.1|552302_553187_+|4-hydroxybenzoate-octaprenyltransferase	unknown	unknown	gnl|CDD|237247
NZ_CP009279.1|WP_156113044.1|561992_562658_+|NAD(P)H-binding-protein	unknown	unknown	gnl|CDD|187560
NZ_CP009279.1|WP_081951013.1|541385_543578_+|choice-of-anchor-A-family-protein	unknown	unknown	gnl|CDD|275059
NZ_CP009279.1|WP_042184493.1|545416_545806_+|NusG-domain-II-containing-protein	unknown	unknown	gnl|CDD|197365
NZ_CP009279.1|WP_042184513.1|558816_559020_+|CsbD-family-protein	unknown	unknown	gnl|CDD|182452
NZ_CP009279.1|WP_081382976.1|560697_561972_+|MFS-transporter	unknown	unknown	gnl|CDD|340883
NZ_CP009279.1|WP_042184505.1|553857_554838_-|heptaprenyl-diphosphate-synthase	unknown	unknown	gnl|CDD|131795

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042184515.1|559189_560602_+|two-component-sensor-histidine-kinase	gnl|CDD|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	1.51988e-57
NZ_CP009279.1|WP_042184509.1|555549_557430_-|DoxX-family-membrane-protein	gnl|CDD|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	3.18406e-128
NZ_CP009279.1|WP_052404135.1|546376_547231_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|275313	TIGR04520, ECF_ATPase_1, energy-coupling factor transporter ATPase. Members of this family are ATP-binding cassette (ABC) proteins by homology, but belong to energy coupling factor (ECF) transport systems. The architecture in general is two ATPase subunits (or a double-length fusion protein), a T component, and a substrate capture (S) component that is highly variable, and may be interchangeable in genomes with only one T component. This model identifies many but not examples of the upstream member of the pair of ECF ATPases in Firmicutes and Mollicutes. [Transport and binding proteins, Unknown substrate].	6.14475e-113
NZ_CP009279.1|WP_042184511.1|557478_558369_-|hypothetical-protein	gnl|CDD|227275	COG4939, COG4939, Major membrane immunogen, membrane-anchored lipoprotein [Function unknown].	1.97875e-05
NZ_CP009279.1|WP_042184519.1|563216_563993_-|tryptophan-rich-sensory-protein	gnl|CDD|376985	pfam03073, TspO_MBR, TspO/MBR family. Tryptophan-rich sensory protein (TspO) is an integral membrane protein that acts as a negative regulator of the expression of specific photosynthesis genes in response to oxygen/light. It is involved in the efflux of porphyrin intermediates from the cell. This reduces the activity of coproporphyrinogen III oxidase, which is thought to lead to the accumulation of a putative repressor molecule that inhibits the expression of specific photosynthesis genes. Several conserved aromatic residues are necessary for TspO function: they are thought to be involved in binding porphyrin intermediates. In, the rat mitochondrial peripheral benzodiazepine receptor (MBR) was shown to not only retain its structure within a bacterial outer membrane, but also to be able to functionally substitute for TspO in TspO- mutants, and to act in a similar manner to TspO in its in situ location: the outer mitochondrial membrane. The biological significance of MBR remains unclear, however. It is thought to be involved in a variety of cellular functions, including cholesterol transport in steroidogenic tissues.	1.88363e-07
NZ_CP009279.1|WP_042123757.1|545789_546347_+|Gx-transporter-family-protein	gnl|CDD|377839	pfam07456, Hpre_diP_synt_I, Heptaprenyl diphosphate synthase component I. This family contains component I of bacterial heptaprenyl diphosphate synthase (EC:2.5.1.30) (approximately 170 residues long). This is one of the two dissociable subunits that form the enzyme, both of which are required for the catalysis of the biosynthesis of the side chain of menaquinone-7.	6.35919e-31
NZ_CP009279.1|WP_042184501.1|550977_552264_+|aspartate-aminotransferase-family-protein	gnl|CDD|99735	cd00610, OAT_like, Acetyl ornithine aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The major groups in this CD correspond to ornithine aminotransferase, acetylornithine aminotransferase, alanine-glyoxylate aminotransferase, dialkylglycine decarboxylase, 4-aminobutyrate aminotransferase, beta-alanine-pyruvate aminotransferase, adenosylmethionine-8-amino-7-oxononanoate aminotransferase, and glutamate-1-semialdehyde 2,1-aminomutase. All the enzymes belonging to this family act on basic amino acids and their derivatives are involved in transamination or decarboxylation.	2.98005e-152
NZ_CP009279.1|WP_042184517.1|562751_563132_+|RidA-family-protein	gnl|CDD|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	3.90843e-65
NZ_CP009279.1|WP_042184499.1|548954_550880_+|peptidase-U32	gnl|CDD|223896	COG0826, COG0826, Collagenase and related proteases [Posttranslational modification, protein turnover, chaperones].	9.12448e-80
NZ_CP009279.1|WP_042184491.1|543750_544686_+|alpha/beta-hydrolase	gnl|CDD|223999	COG1073, COG1073, Hydrolases of the alpha/beta superfamily [General function prediction only].	5.87915e-23
NZ_CP009279.1|WP_042184497.1|548119_548911_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	gnl|CDD|223692	COG0619, CbiQ, ABC-type cobalt transport system, permease component CbiQ and related transporters [Inorganic ion transport and metabolism].	2.01581e-37
NZ_CP009279.1|WP_042184495.1|547221_548127_+|energy-coupling-factor-transporter-ATPase	gnl|CDD|275314	TIGR04521, ECF_ATPase_2, energy-coupling factor transporter ATPase. Members of this family are ATP-binding cassette (ABC) proteins by homology, but belong to energy coupling factor (ECF) transport systems. The architecture in general is two ATPase subunits (or a double-length fusion protein), a T component, and a substrate capture (S) component that is highly variable, and may be interchangeable in genomes with only one T component. This model identifies many but not examples of the downstream member of the pair of ECF ATPases in Firmicutes and Mollicutes. [Transport and binding proteins, Unknown substrate].	1.94146e-125
NZ_CP009279.1|WP_042184503.1|552302_553187_+|4-hydroxybenzoate-octaprenyltransferase	gnl|CDD|237247	PRK12886, ubiA, prenyltransferase; Reviewed.	3.05526e-85
NZ_CP009279.1|WP_156113044.1|561992_562658_+|NAD(P)H-binding-protein	gnl|CDD|187560	cd05250, CC3_like_SDR_a, CC3(TIP30)-like, atypical (a) SDRs. Atypical SDRs in this subgroup include CC3 (also known as TIP30) which is implicated in tumor suppression. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine rich NAD(P)-binding motif that resembles the extended SDRs, and have an active site triad of the SDRs (YXXXK and upstream Ser), although the upstream Asn of the usual SDR active site is substituted with Asp. For CC3, the Tyr of the triad is displaced compared to the usual SDRs and the protein is monomeric, both these observations suggest that the usual SDR catalytic activity is not present. NADP appears to serve an important role as a ligand, and may be important in the interaction with other macromolecules. 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. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. 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. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	4.75336e-80
NZ_CP009279.1|WP_081951013.1|541385_543578_+|choice-of-anchor-A-family-protein	gnl|CDD|275059	TIGR04215, conserved_hypothetical_protein, choice-of-anchor A domain. This domain may occur as essentially the full length of a protein, except for an N-terminal sequence and a C-terminal protein-sorting signal such as PEP-CTERM or LPXTG. Most often, the putative surface protein is longer and contains repetitive sequence regions. This is one of very few domains for which both anchoring domains occur, and designated choice-of-anchor A domain. The best characterized member is Bacillus anthracis protein BA0871, a collagen-binding protein with five CNA-family protein B-type repeats toward the C-terminus and an LPXTG cell wall attachment motif.	7.4987e-61
NZ_CP009279.1|WP_042184493.1|545416_545806_+|NusG-domain-II-containing-protein	gnl|CDD|197365	cd09911, Lin0431_like, Listerrria innocua Lin0431 is similar to the N-Utilization Substance G (NusG) N terminal (NGN) insert (DII). This family contains domains homologous to Listeria innocua Lin0431, a protein that is similar to the N-Utilization Substance G (NusG) N terminal (NGN) insert (domain II, DII). Lin0431 and Aquifex aeolicus NusG DII (AaeNusG DII ) have similar structure and similar basic charged surface distributions that may bind negatively charged nucleic acids and/or another anionic binding partner, suggesting a possible role in transcription/translation regulating functions. Despite these two domains having low sequence similarity, the NusG DII and DUF1312 domain families may have diverged from common evolutionary ancestral proteins, and may have similar biochemical functions.	2.50877e-35
NZ_CP009279.1|WP_042184513.1|558816_559020_+|CsbD-family-protein	gnl|CDD|182452	PRK10428, PRK10428, hypothetical protein; Provisional.	5.2352e-16
NZ_CP009279.1|WP_081382976.1|560697_561972_+|MFS-transporter	gnl|CDD|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. 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 SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 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.	5.98027e-20
NZ_CP009279.1|WP_042184505.1|553857_554838_-|heptaprenyl-diphosphate-synthase	gnl|CDD|131795	TIGR02748, Heptaprenyl_diphosphate_synthase_component_2, heptaprenyl diphosphate synthase component II. Members of this family are component II of the heterodimeric heptaprenyl diphosphate synthase. The trusted cutoff was set such that all members identified are encoded near to a recognizable gene for component I (in pfam07307). This enzyme acts in menaquinone-7 isoprenoid side chain biosynthesis. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	5.56476e-80

Protein sequences

>NZ_CP009279.1|WP_042184503.1|552302_553187_+|4-hydroxybenzoate-octaprenyltransferase
MAILNIFKTAGLKLKMFSELVMFSHTLFSLPFAIISMVWAAGGWPSGHVMIWGLIALIGARNGANAFNRLADRTFDEQNPRTAHRHLPQRLLAEKEVVVFVIVNYAIFIVASGMLNLLCMILSPVAIVLISTYSYTKRFTFLSHLYLGFVIASAPIGAWFAVTGNIAFTPFVIGTVVMLWIAGFDIIYGTQDIEFDRRHGLWSIPSFFGLENALRIAKGLHFIMIMLLLFLYLWRDLGWMYLVGIGIATLLLMTEHKIIKPSNRKLMKVASYNLNQVISIVILLCTLIDFFYVS
>NZ_CP009279.1|WP_042184501.1|550977_552264_+|aspartate-aminotransferase-family-protein
MEQQDFIGREAVAAKRKQYFYPCTQHFYRDAPQLVRGSMQFVYDEKGKSYTDFFAGVSVVACGHCNPAITVRTIEQLQQLQHTTTIYLTQPSVDLAERLEEVMPGGLRRTFFVNSGSEANEGALLLARMYTGRKGFIALESGLHGRTNLTMSVTGLPMWRTDKYLDHDVEFIPRPYHPDLSLEEAASLSLESLERVLEEKGNTIAAMIVEPIQGNGGMIMPTRTYFRDVKALLERYGVLLIADEIQTGFGRTGKMFAMEHFDVVPDIISMAKALGNGIPVAAFATTDEIALALNRPSASTFGGNPVSAATALAVLDYIRDERLPERSVQLGERLKAGLKALQARYPSMIVDVRGTGLMLGAELTGVDAEGAAALTDQVLEAMKDRGYLIGKNGIGRNVLAFQPPMIITEEDIDGMLDVLNEVLAELND
>NZ_CP009279.1|WP_042184499.1|548954_550880_+|peptidase-U32
MARYFNGREIELLAPAGTFEIFKEVIQARCDAVYFGGPVLNMRMMRKGYNLSHEEIVEALDIAHRLDKKVYITVNNLFSEEDVEEAKEYLRFLDGARPDALIVQDMAVLELIREMELNLPIHSSVMMNVHNLEMIYALRDLGVSRVVTSREMDLQTAKLLGQRSGMELEYFIHGDMCSVHGANCYFSSHVFGMSSNRGKCMKPCRWDYRVKKDGYVYPAEYPLAVKDMFMYEHLPELIESGITSFKIEGRMRDKEFMVMLANSYGEAIDRYIDDPIGFDRTVDTKELHNNRKRDFSTAYAFGKPGLTNINRRYEGTGKFYSTGKVFSTPTAERELSEKRVEQLRERLAEVEQPQKTKAKLAVRVNNMEQARMVLELGVDSLYLPGDVFEPDKPFTKRDIKELGELKGDSKIYLGLPRMMTELHFDQYDQLLGGERLPIDGIIVTNLGAIRRYNNTGYPLIGDSNLNVYNHLSAQLYANLGLTQLSVSPEMTLEHFATFASRCKTPLEVVVHGTPALMYMEHDLYENTELMEPIAEEDNQYVHNNVLVLKTDQGENPVYRDQHGRCHLLFAKELCYLPLLSEMSGLGISSFRIEGATYSVEQLREIIVSYQQAINGSDSGDDMLGGLKPVYAGYTLGSLQFN
>NZ_CP009279.1|WP_042184497.1|548119_548911_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT
MNEKLIIGRSIETGSWVHKLDARAKITGMLLYVAVILLSRSWMAMALLAIFSIAVMASTRIPLKYFLKAAKPLRYLMLFIFIVQLLSVKTGEAVLTLGSWSIYEGGLRLGAFSVIRMFFLITFTALLTFTTTPGKLNQGLEGILAPFKKFGLKPDRITLMISISLRFIPTILDESQIIMKAQASRGADLKELPLKEKGRMLVSLLVPIIASAFRRAQDLVYSMEARGFRMDAPRSQYHRLRWGIFDTIFITMFIVMGIAVALV
>NZ_CP009279.1|WP_042184495.1|547221_548127_+|energy-coupling-factor-transporter-ATPase
MAIELQQVSYSYADRSLWKLTALRDINLSVPTGSMVGIAGATGSGKSTLLQLFNGILKPTEGTVKVLDVTIQAGEKSPKLMPLRRRVGLVFQFPEQQMFEDTVEKDLIFGPLNFGMSLEEAKARARQAMLDMGLDLALLERNPFKLSGGQMRKAAIASVLAMDPEVIVLDEPTATLDPISRAELIHLLERLCREQGRTIIVVTHRMDELLPYADNWLVLKEGSTAFQGSVKALADDPSILEQCGLTVPQSLRYWRAVADRFGLTDEAPRLTAESLAELIASLPSGSGNSSEQHEGKRDGHE
>NZ_CP009279.1|WP_052404135.1|546376_547231_+|ATP-binding-cassette-domain-containing-protein
MNESYEGQELEGEGQAIISLDGVSFGYDPEHPILQNITLSISQGQWVSLVGPNGCGKSTLVKLLNALLPKSAGEIVVSGMQLSEETIGSIRQCIGMVFQNPDNQFIGATVEEDILFGLEGLCLSYEEMAERLHSYTTRLGINHLLSKHPGELSGGQKQRVAIASILAMEPGIVIFDEASSMLDEGSRNDLLGILQDMRAEGKYTILMITHDADEILASDRVLALHGGGLAADVTPAELFRNEELLQKCHLCEPYPWRLARELQNQGIHVDVPASEKELIDTLWP
>NZ_CP009279.1|WP_042123757.1|545789_546347_+|Gx-transporter-family-protein
MPMSSSESATALKRTVIIAIFAAVAVVLSLIEAQIPLSGMGLVPGAKLGLANIMILTCIYFLRGRDAFLLVILKTLLTAFLLGTFSSLLFSLFGSLFSFVVMFVLMLISGKGKSISLIGISIAGGIAHNIGQLLAASMVFSSLSIFYYLPMLLITGVVTGIAVGYAVRYLVASLSKISLFEEFLD
>NZ_CP009279.1|WP_042184493.1|545416_545806_+|NusG-domain-II-containing-protein
MKRADVWLISIVLIAALAFLAPRWFSDNDDKGGAGKNLVANVTVDGELFKTVKLTKEEQTIEVRTERGYNLLKVHDYGIEMYDADCPDQVCLGFGFITLPKQTIVCLPHRVLVEITSASGEDDIDAYVQ
>NZ_CP009279.1|WP_042184491.1|543750_544686_+|alpha/beta-hydrolase
MVWFFISAVIAIGALIYAGFFFYGIAIKRAPKEFLSNNRDLKVDPPVAGASWGEGKDWISSQSFENVEITSEDGLQLRGYLLLSDRAEGRTAILAHGYSGKGKDMGAYAKIYYERLGFNILIPDARGHGESAGNYIGFGWHERKDYLQWIDYIIEKTGPSAQVVLHGVSMGGATVLMTSGENLPPQVKAIVSDCAYSSVKAQLAYQLRRMYRLPSFPFIQSASLITRLKAGYGFSEASALKQVRKAKVPILFIHGDADNFVPYSMMNELYEACQSPKEKFVVPQAGHGLAYDMDKTGYINVVTVFVNQYVN
>NZ_CP009279.1|WP_081951013.1|541385_543578_+|choice-of-anchor-A-family-protein
MKRRMKPLLALVLAGILTVGSGLSGGHLVNAAGEVLPYTPTPVLGIAGNFNTFIFGDFKQSNDQVHGRLAAKGNITLQNYGVSKDNPGGDVLIAGNDISFTNGTVHGASVYGGVFSSNGVDLKEPARKGTPIDFDAEEQFLIGRSNEFSSLATIGTFKKEYGKITIDASEPFNVLNLSAADFAGANGLQFNIANSATVIINVSGSSVNIPSFQIWGGSPNKVLFNFYEASTVDIGSLTIEGTILAPLAKVTYNSGELHGTLIAKGFAGGVQMHWYPYGGEEPPPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTPTVTPTPCVTPTPKPTPTPKPTHTPKPTPTPKPTHTPKPTHTPKPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPIVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPTVTPTPTPSPEVTPTPTPSSEVTPTPTPSSEVTPTPTSSSEVTPTPTPSSEVTPTPTPSSEVTPTPTPTPEPPVFPTPTPSFVIGTIIVNDDPVPLGPVASSTPALVPTPTPSSNTEVLVDDEEIPLGPVLTVTPTPSPEDIAVVDDTIPLGNPPVDELPKTGESSSVPYYVTGLGFALIGLLMRNRFSSKK
>NZ_CP009279.1|WP_042184505.1|553857_554838_-|heptaprenyl-diphosphate-synthase
MKLHEALNIDIDEINREIVNLVARDKDVPKKSQLGQSVLELINSGGKRLRPLMVIVGSRFGRKDTGRRALQLAAAAEFIHVASLIHDDIIDDSELRRGKPALHTKTGTLSAVHIGNYMSARVIELLSKYTGDKNKYVHDLSSVATAQLCLGEYQQMEHAFDYEITMEQYLEKSLNKTALLMATCLRVGALSTESSEEVADLLYTFGEALGMSFQIQDDLLDFTQSEAVLGKPAGSDLRHGQVTLPVLYALQDPKLSPVIRSIGPDSSDAEVAHVLALIKRSDALARAEQFSQNYLDKAGAIVQQLSSYPAHADLDTLLQYFADRDR
>NZ_CP009279.1|WP_042184507.1|554855_555305_-|hypothetical-protein
MNKQLIEDTLRLLHTEMSPIAGIELNPSPAACEQLISVLERHDLEYNRKVNLLGIYTILTLAAERHMECIPHHPDLTRNILDGDYLYSFYLQFAVKCRELDLVAYLAPSIKKMQIRRSNGDFAEHDPAAGIEQFLIQECRQRSRTSKAI
>NZ_CP009279.1|WP_042184509.1|555549_557430_-|DoxX-family-membrane-protein
MKKIVILGGGYGGVLTAKKLAKKFKKNKDVEITLIDRNPYHTLLTELHEVAANRAPEDSIKIDLKKIFAGLKVNVVLDEISNIDFKGKKLKSNKTTYAYDYLVIGTGSKPTFFGIPGAEENTFSFWSYDDAVALKRQIRDMYTKAAMEKNPTVRRAMLTFVIIGAGFTGVELVGEMAEQREELCKEFYIDPSEVRLIVADMAPKILPILPDKLIQKAEAHLRKLNVEIVTGAKITEVGEGSVALGEKNVVASQTIVWTAGVEGSEIVGGLEVQQQGRKRIVTNENLESVDHKNVYVVGDNIFFIPEGETRPVPQMVENAEQAAPIVAGNIAADIQNTAKKAYKPGFHGTMVSIGSRYGVANVGLPGKFFMLTGFMAMLSKHFINMFYLSQVVGFNKVWTYMMHEFFHVENRKSFLGGHFSKRSPNFWLVPLRMLLGGMWLYEGIDKLRKIWVDPNKIFLIPAAPFATDASSAASVAVDAVKTTVDAQSAASAVSTAKEAVEALPVPGFVYNITNWFMDLMFYNNDGSYTFLAKWFQIGMVCAEIVFGIMLIVGLFTAIASIATIAMSVMIWSTKMASTEMLWYVGAGIACIGGSGSTFGLDYYVLPWLKKHWKRVPIVRRWYLYTD
>NZ_CP009279.1|WP_042184511.1|557478_558369_-|hypothetical-protein
MKKTTVILSTALILGSLLAGCGNNTDNTPAATNAPTENSTATNSTNTGTEAATYKDGTYYATADVDAKTGWQYFALLTVEGGKITKADWDAFNVNTAGDLKKKVSEDGKYGMKAGGASSEWHEQAAKAEAFLIEKQDPAAITLDAEGKTDAISGVSVHVSDFVKAAQAALAAGPVEAGQYKDGGYHAEGEMDKDSGWKSTVDLTVANGNVVAVKFSGVNAAGDDKKQFSVDGKYGMKAGGASAEWHEEIAKVEQYYLEKGTAPELTAEGKTDAISGVSIHVGEYFTLAEKALEGAK
>NZ_CP009279.1|WP_042184513.1|558816_559020_+|CsbD-family-protein
MDNNVFKGKWKQLKGEAKKQWGKLTDDDLDVIDGEKDKLVGKLQERYGHSKEDAEKEYQSWGRSYRD
>NZ_CP009279.1|WP_042184515.1|559189_560602_+|two-component-sensor-histidine-kinase
MGYLKIFFGNTAILIAVAYLANLIYKHTISNASVGIKKASWVILAIFAGWISTLFGYNLDDHVIFDLRFVPLIISTLAYPRPITLILIGIGTGLTRLTFGVTEAAVAGMLNLFILGVICAALSYWVRRSTLSIVNQGLIVILIVNLMNAINIMALGVIPVEEYIREIMPITFPAGLILSILFSLIIRDFQLGLLRNEQIQHANEQLSAQTEELHKNKLDLEERANQLMMASQFKSEFLANMSHELRTPLNSIINLSQLIEENDDLLTEAEIREYAAIIHRSGDELLMIISDILDLSKVEAGRLDIINEELNVSEIPDLLAMQFAVTAKQKGLAFNISMDENVPPMIHSDPHRVQQILRNLLSNAFKFTKTGFVSLHIHEQEGGEGDAVQHWLVFDVEDSGIGIAPEKHAMIFEAFQQADRTTSRKYGGTGLGLSISNDLARLLGGFISLESKEEKGSRFSLYLPLEVDSE
>NZ_CP009279.1|WP_081382976.1|560697_561972_+|MFS-transporter
MDNMENKHKVTVSKRVRKPSVHRRNLRIATLEGVPSTIFQVLLQGQFLTGFLLYLGASSSQIGFVLALTTLVNVAQIGVAFLIQKLPSRKWAMVTFIGLHRILWGSTGLIPFIFPKEYWVIAFIALYTTAFIANTAGGVLWSSVISDLVPARVRGRYFGIRNTVLNALGSLVMYGGGIILDRYPGGHGFLILYIVVWIFSISNVVVFFFYPDVPFEKSEEHKFLPMFKKPLKDTLFMKSTLFLAAWLLLQNLTVPLYSYVMLQLLHINYETLSLLNVSQTVFMMASFYVWGNLNAKYSNKRLLFFTLPIIALSSLMWGLLSVMPMLVVLFAAHIVFGVGVGGFNQLAFNFIIGDTPKKERPMYMATYAALTGLSSFFGPLIGGQLYEKIAHWPQWTQVYGMQLVVGTLMIALAFLLGRRILKDE
>NZ_CP009279.1|WP_156113044.1|561992_562658_+|NAD(P)H-binding-protein
MLRIAMVLGATGLVGKAVTEELLNRDNWEEVRVLVRTPLAMEHPKLKQIVVDWENLRNYTESFEGVHSIFCCLGTTIKKAGSQEKFERVDLHYPLDAAAIAREQGVKQFLAVSSIGANAKSRNFYSRTKGRAEEGLTAIGFQGMHIFRPSLLLGQREEFRLGERVGASLMKALDFVMVGKAAKYRAIPGTTVARAMVNIASADTHGLHIYTNEVIHVIGKR
>NZ_CP009279.1|WP_042184517.1|562751_563132_+|RidA-family-protein
MSKKQVATTKAPGAIGPYSQAITTGSWVYTSGQLGLNPETGNLVEGVQEQARQALNNVQAILEEAGATLDHVVKTTVFLKDMNDFAAVNEVYSTFFKEPYPARSAIEVARLPKDGLVEIEAVARKK
>NZ_CP009279.1|WP_042184519.1|563216_563993_-|tryptophan-rich-sensory-protein
MRRYNPYKWWNLLFFLGVIIVNVLSVTLPLGGHSTGEISDKYQTYITPAGYAFSIWSLIYLLLAGFIIYQFRSYTASRDSVRAVQFWFVLSCIFNMSWLFLWQYLYIELSLVAMVLMLITLIVIYRKTRLIANPTSGEKWLMKLPFSIYLGWISVATIVNISVVLEKNHWGGWGLSGSTWGVIMLCVGTLLAIVVSYPYRDSIYPLVFVWAFIAIALEHKETSDVYLTGMITAGLLLLYSIWLLFKPRRSRYRRYRSY

Crispr_ID: NZ_CP009279_2

• CRISPR_ID: NZ_CP009279_2
• CRISPR_location: 1080489-1080591
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_2

Consensus_repeat	Method
CGAAGTCAAATCATTGAAGCTAATGCTCACAAAACTT	CRISPRCasFinder

spacers of NZ_CP009279_2

>2.1|1080526|29|NZ_CP009279|CRISPRCasFinder
AAGTTTATGCTTTCGAAGTGAGTTTTGTA

CRISPR arrays and Neighbor proteins around NZ_CP009279_2

CRISPR arrays

The CRISPR arrays of NZ_CP009279_2

>merge|NZ_CP009279|2|1080489-1080591|CRISPRCasFinder
CGAAGTCAAATCATTGAAGCTAATGCTCACAAAACTTAAGTTTATGCTTTCGAAGTGAGTTTTGTACGAAGTCAAATCATTGAAGCTAATGCTCACAAAACTT

>NZ_CP009279|2|2|1080489-1080591|CRISPRCasFinder
CGAAGTCAAATCATTGAAGCTAATGCTCACAAAACTT	AAGTTTATGCTTTCGAAGTGAGTTTTGTA
CGAAGTCAAATCATTGAAGCTAATGCTCACAAAACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042131858.1|1071646_1071889_-|NHLP-leader-peptide-family-natural-product-precursor	unknown	unknown	gnl|CDD|274786
NZ_CP009279.1|WP_042185176.1|1086749_1088135_+|oligosaccharide-flippase-family-protein	unknown	unknown	gnl|CDD|240533
NZ_CP009279.1|WP_036676609.1|1083192_1084539_+|O-antigen-ligase-family-protein	unknown	unknown	gnl|CDD|377422
NZ_CP009279.1|WP_042185173.1|1082247_1083183_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|366154
NZ_CP009279.1|WP_042185166.1|1079093_1079834_+|capsular-biosynthesis-protein	unknown	unknown	gnl|CDD|226453
NZ_CP009279.1|WP_042185179.1|1088161_1089019_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133005
NZ_CP009279.1|WP_052404164.1|1085305_1086784_+|O-antigen-ligase-family-protein	unknown	unknown	gnl|CDD|377422
NZ_CP009279.1|WP_042124430.1|1081529_1082222_+|sugar-transferase	unknown	unknown	gnl|CDD|376775
NZ_CP009279.1|WP_036676606.1|1084535_1085309_+|WecB/TagA/CpsF-family-glycosyltransferase	unknown	unknown	gnl|CDD|377136
NZ_CP009279.1|WP_042185152.1|1073019_1073313_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042185164.1|1078192_1078828_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP009279.1|WP_081951039.1|1075340_1076204_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197666
NZ_CP009279.1|WP_042185181.1|1089005_1090193_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_CP009279.1|WP_042185151.1|1071980_1072916_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042185171.1|1080608_1081499_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU	unknown	unknown	gnl|CDD|224131
NZ_CP009279.1|WP_042185158.1|1076520_1078167_+|histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_CP009279.1|WP_042185169.1|1079817_1080459_+|CpsD/CapB-family-tyrosine-protein-kinase	unknown	unknown	gnl|CDD|349772
NZ_CP009279.1|WP_042185153.1|1073354_1075265_-|family-20-glycosylhydrolase	unknown	unknown	gnl|CDD|119335
NZ_CP009279.1|WP_042185147.1|1069710_1071630_+|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|223715
NZ_CP009279.1|WP_042185183.1|1090192_1091332_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042131858.1|1071646_1071889_-|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].	2.77264e-15
NZ_CP009279.1|WP_042185176.1|1086749_1088135_+|oligosaccharide-flippase-family-protein	gnl|CDD|240533	cd13128, MATE_Wzx_like, Wzx, a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Escherichia coli Wzx and related proteins from other gram-negative bacteria are thought to act as flippases, assisting in the membrane translocation of lipopolysaccharides including those containing O-antigens. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	4.71254e-36
NZ_CP009279.1|WP_036676609.1|1083192_1084539_+|O-antigen-ligase-family-protein	gnl|CDD|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	7.18583e-09
NZ_CP009279.1|WP_042185173.1|1082247_1083183_+|glycosyltransferase-family-2-protein	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.	7.73981e-28
NZ_CP009279.1|WP_036676606.1|1084535_1085309_+|WecB/TagA/CpsF-family-glycosyltransferase	gnl|CDD|377136	pfam03808, Glyco_tran_WecB, Glycosyl transferase WecB/TagA/CpsF family.	7.05131e-85
NZ_CP009279.1|WP_042185179.1|1088161_1089019_+|glycosyltransferase-family-2-protein	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	8.90289e-68
NZ_CP009279.1|WP_052404164.1|1085305_1086784_+|O-antigen-ligase-family-protein	gnl|CDD|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	7.34179e-08
NZ_CP009279.1|WP_042124430.1|1081529_1082222_+|sugar-transferase	gnl|CDD|376775	pfam02397, Bac_transf, Bacterial sugar transferase. This Pfam family represents a conserved region from a number of different bacterial sugar transferases, involved in diverse biosynthesis pathways.	1.99577e-97
NZ_CP009279.1|WP_042185147.1|1069710_1071630_+|GHKL-domain-containing-protein	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.91261e-41
NZ_CP009279.1|WP_042185164.1|1078192_1078828_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.68454e-63
NZ_CP009279.1|WP_081951039.1|1075340_1076204_+|AraC-family-transcriptional-regulator	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	1.07548e-21
NZ_CP009279.1|WP_042185181.1|1089005_1090193_+|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.	5.02139e-66
NZ_CP009279.1|WP_042185171.1|1080608_1081499_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU	gnl|CDD|224131	COG1210, GalU, UDP-glucose pyrophosphorylase [Cell envelope biogenesis, outer membrane].	2.93262e-170
NZ_CP009279.1|WP_042185158.1|1076520_1078167_+|histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.2967e-28
NZ_CP009279.1|WP_042185169.1|1079817_1080459_+|CpsD/CapB-family-tyrosine-protein-kinase	gnl|CDD|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	1.72205e-63
NZ_CP009279.1|WP_042185153.1|1073354_1075265_-|family-20-glycosylhydrolase	gnl|CDD|119335	cd06565, GH20_GcnA-like, Glycosyl hydrolase family 20 (GH20) catalytic domain of N-acetyl-beta-D-glucosaminidase (GcnA, also known as BhsA) and related proteins. GcnA is an exoglucosidase which cleaves N-acetyl-beta-D-galactosamine (NAG) and N-acetyl-beta-D-galactosamine residues from 4-methylumbelliferylated (4MU) substrates, as well as cleaving NAG from chito-oligosaccharides (i.e. NAG polymers). In contrast, sulfated forms of the substrate are unable to be cleaved and act instead as mild competitive inhibitors. Additionally, the enzyme is known to be poisoned by several first-row transition metals as well as by mercury. GcnA forms a homodimer with subunits comprised of three domains, an N-terminal zincin-like domain, this central catalytic GH20 domain, and a C-terminal alpha helical domain. The GH20 hexosaminidases are thought to act via a catalytic mechanism in which the catalytic nucleophile is not provided by solvent or the enzyme, but by the substrate itself.	1.07077e-92
NZ_CP009279.1|WP_042185166.1|1079093_1079834_+|capsular-biosynthesis-protein	gnl|CDD|226453	COG3944, COG3944, Capsular polysaccharide biosynthesis protein [Cell envelope biogenesis, outer membrane].	1.35871e-41
NZ_CP009279.1|WP_042185183.1|1090192_1091332_+|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.	1.23019e-51

Protein sequences

>NZ_CP009279.1|WP_042185169.1|1079817_1080459_+|CpsD/CapB-family-tyrosine-protein-kinase
MLRLNKSLVTDVNPSSHISESFRSLRTYIRQLGIAQGSGGKVLLFTSAEAGAGKTTILSNLAVSFVQDGKKVAVVDCNLRHPGLHTVFEVEGSDGLAAYLSGQEEADNIAVLGNLANLSVIPAGKTHVSPPDLLGNPKMTALLEELKENYDLILLDSPSAVDFSDARILAPQADGVILVARYGKSKRESIRKAKTLLEQTGSNLIGIAMNQAK
>NZ_CP009279.1|WP_042185166.1|1079093_1079834_+|capsular-biosynthesis-protein
MEKTILDYINLIKKRFWLIMVFVLISCATTYYVSKNFVEPVYSASGQLLVNNIAKAPESNNLNDLSFSLNLIESYKEIMKSPTIMKSVIENHPEFGLTADELSQKLEIKTSEKSQVINLNVHDENYTKAAGIVNAVSQTFIRELPSLMRVDNVTLLTPADPTDVPGPSNGGFAMNLIISFVVSLMAALGIILLMETLNGTLRSEKEAEYDLGLPVIASIATIRKRDLGKAAGGNTRVKEGAYVAAK
>NZ_CP009279.1|WP_042185164.1|1078192_1078828_+|response-regulator-transcription-factor
MKIVIVDDHPLVRRGLASVISMQPNVKFAGEATNGQEALLVIEETQPDLVLIDLKLADESGLDVIKKARARGIVSKFILLTSSASREDFLKAEEVLVDGYVLKEALPEELLFAIQLVHKGRKYYDPGLMEDKMRMSESSPTDELTPKEKEVLIELGQGACNREIASRLFISEFTVKKHVSQILAKLQVADRTQAALYANAVGLTKYEMSYE
>NZ_CP009279.1|WP_042185158.1|1076520_1078167_+|histidine-kinase
MKIKPTAEDKLIEYYRYFSLSLTSLMYLLDKTGPSVIYKSLVIAILFLFAQTFSFFYRRLRSRPKTLVLAVSIEMVGIIALTLFTGGYESSFRLYVLNPVLIAAGSLSIYFGWSLLLSYISIFAVLCYFFINSANKTFLEIVFVNGNLFLTLVLTVIIMQIVNRMKRQREESNARTKETMEHIKSLYHIVETSSQHDFMNIGQVITDYVVKLTKLDKALFWFAKKSGEPAPQSRQTGWQQEEEQFLFSELGKHEHEWRLQREPIFRNLPGLGDFLLMPVRMSTRFVGMIGLKLESTEGLEGRRWYIQQLIFLSELSANILERHELGVIENRLIITNEQNRIADEMHDSVSQSLFGIVYATHSLKESWKRMSDHELEEQIELIHDSATKVAKELRITIYSLSSKKSGGPTWLGMVRSHLKSLSRLNDVDIELKITGDDFSLPYPYHKALFRIISEATGNAIRHGAASRVDVELSLKPTWIRLLICDNGVGFDTDLLWIESEDSASGLGMKNMQYLTQSLGGDFQLSSNENMGTRILISIPVGVAELKNA
>NZ_CP009279.1|WP_081951039.1|1075340_1076204_+|AraC-family-transcriptional-regulator
MSIMSKRMDYMISPYPIRIIDPKVESSKLKLKNIRVGQAGHLPGRTLFRSGVVFEHWAIVYIVSGGGTYMETSGKEQQVREGSLFFFRPGYSYNFGPPPGGSWDEYYINFNGTRVSEWLESGLIAGGNVFQANSIMGLSTLFEEVLQRMESGEPADADRAALLVERMLLECSFIIEEKSWNAQADYMRQIREDLNLCIYGEMDLEQIAAKHHISMSTLRRLVRRSSGYPLHEYIHRLKMAEAKKLLLNTSLQVKEISGMLHYNDPFYFSRLFKKYMGIAPQLCRSNI
>NZ_CP009279.1|WP_042185153.1|1073354_1075265_-|family-20-glycosylhydrolase
MLNHSTLLLLPNPREITLSQDSYRFPISGSIVLPSTGEQSSMPAAQKLQAVIKQALNLHLTLSIGTRPTVVSACIFSYVPSLSEQAYEIVVDQSGIVVSYSSPVGAFYAAATLKQIIEQSGRSIPHLHIRDEPDFGARGITVDISRNKIPKQETLYRIIDLMADLKMNQLQLYIEGTPFAYESFPQVWELETPITGEEILLLDAYCKARYIELVPNQNSFGHMEGWLSRPEFNALAEIPEGFMLPKELYMGDVYPEGLFMHPGTFDTEDPAVLPLLEKMFDDLLPYFSSNQFNVGCDETYELGLGKSKALAESQGKGQIYLSFLQKIYELVTKRGKTMQFWGDIIIQHPELIPHLPKDIIAMEWGYSAEHPFESDTLKFREAGIPFYVCPGTSSWNSITGRSDNMFANLRSAAIHGKNNGSIGYLITDWGDHGHWQHLPISYTGYVYGAALSWNVDNNLDVDTAKYLNTFIFADRSEGIGQLLLDLGNYYQLESEIIRSNDTEMSLLLRTNLDNLLIVEKLTEEHFNNLEEYMLSIEARLSGLDLQCADADLVLKELSNGIHFVKHAVQLGRIKLQLASAPDSIDPNLITEQINDLNILLHQYRLLWTERNRLGGLDQSIWRLLRLRGQYEALKSK
>NZ_CP009279.1|WP_042185152.1|1073019_1073313_+|hypothetical-protein
MDCYTFGQMLMTIRMGQKAETPDGRIVMRTSAGLIWTNGILNGKTVEIKDYLFSDLWQIYEDEESMKEGIGREKHEKREREMLENQYEELRLASRKH
>NZ_CP009279.1|WP_042185151.1|1071980_1072916_-|hypothetical-protein
MDWLNDYEEELRLVFQESRKIISEFPEPLNSQGMSYLEHFNVFNAESHKNYICYLLPFWLQKSCGLSAEITRQMSMGNVFFMLYFFIQDDLMDSKESSTYERLPLANLLYVEFLNIYRLLFTNDSSFWTSFNRYIAQWADSVSNETTSDYFLNDRIKIPYKASPLKLSSTAALLLSGKDSLVPQSEEVIDSVLLTLQMLDDYEDWNEDLSEGSYNCLLSLTRSYLSTDKATTLTSKEVEFFLFTANGLRTYAELAQDTHRKVMASSLDIPHLLAFHSMLVTNLQQISDSIEAEKQLLQGGGLFYYLSKNIQ
>NZ_CP009279.1|WP_042131858.1|1071646_1071889_-|NHLP-leader-peptide-family-natural-product-precursor
MMSEAVLRNQVIQKAWEDPSFKQRLLADPKAALQEALGVIIPDSVTLKAVEEGSNEFYLVIPPSPSSDVLKATAAPRGSW
>NZ_CP009279.1|WP_042185147.1|1069710_1071630_+|GHKL-domain-containing-protein
MRLMVRILHITITLSLLLIGCGSIIVSAANPNPSHEITKWQMKWEDETGNTGQEIPWSEGQQSWMNVDSKKELPELPSGVSSSWTRISLPDLSYVSPSVYIDTLYALHVRVYVEDRLIFEENRKYIKDNYSLLLPLSKEDNGKTLYIWTETMQDRIGIKKSVMIGEHSQLINEYIENGLSDVILGCAFFLVAIVLFISALYINRDYFSSVASLAVVIAATGILSITYSPFIYTFYNKLGPISNVCLDLALFSLLPALTFLFEKLFGSGKFSIIRKFRQFQVLYSSFCLLCLLINLLSNNRYIEFYYFISTTIIGVILILQFILLIACVVMFSLKGNKDAIVFAIGFGTAAFTVVAELLWYYIQKGNYDLFLWKWGLVAFIISLIVILERRLAYNHQQVVNYSRELERFNNELERSEKMEIISELAASVAHEVRNPLQVTRGFLQLLSEKSVNEEQIYMSMALSELDRASNIITDFLTFAKPEFETISSLNLYDEFKHIESIMQPLCHINGGKMILDVSGQLWVKGNSSKFKQAFINIIKNSIESFSEEGFIYMSVYGEDNKVIIHIKDNGEGMDPDVLHRLGEPYFTKKNKGTGLGLMVTFRIIETMQGEVRFTSKKGVGTESITILPLAEAPDDSYSL
>NZ_CP009279.1|WP_042185171.1|1080608_1081499_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU
MKKVKKVIIPAAGLGTRFLPATKAMPKEMLPIINKPTIQYIVEEAIASGIEDIIIVTGKGKRAIEDHFDNAFELESRLLEDGKLDLLKEVQRSAKVEIHYIRQKEPKGLGHAVWCARRFIGDEPFGVMLGDDIVTGAVPCLKQLIDQYEETQNSVIGVQEIPDEFTNRYGIIEPDLQDGKLYRVNNFVEKPPLGTAPSNLAIMGRYVFTPKIFKYLDLMEEGAGGEIQLTDAIQKLNQSERVYAYNFDGTRYDVGERLGYILTTLEFALQSEDLRYPVMDAMAEWLNKMGQTSLSS
>NZ_CP009279.1|WP_042124430.1|1081529_1082222_+|sugar-transferase
MSMQKLPEDYEAVLPKLYMLHTDERRKEAESYLIMKRMIDIFFSALGLLVLMPLFVVVAILIKLEDPKGKVFFRQNRVGKNEKQFPMYKFRSMVSNAEELKENLMAYNEVSGAMFKIKNDPRITQIGRFLRKTSIDELPQLWNVLIGQMSLVGPRPPLPEEVAQYTEYDKQRLTVTPGCTGYWQVNARNSVGFDEMVQLDLTYIHIRSTMLDLKIIAKTGLMLLGSKDAY
>NZ_CP009279.1|WP_042185173.1|1082247_1083183_+|glycosyltransferase-family-2-protein
MREYGDVPKLSIIICTYNRAPLLIKTLQSLLKLDHLEQAEIIVVDNCSKDDTEACVKKFIGKHGADMDIRYMMEPMQGLSAARNTGILASKSPLIAFLDDDAIPCQRWITTIVSTFESKPEVMAMGGKIAPIFESKRPDWLIKPFELPYTIVDLGSRIKEYPKQLHPCGANMAMRKLVFDISLFPLDLGRKGDSLLSGEETWLFGQIQKEGHSILYHPEMAVDHFVPAARLTEDWIMRRYYSQGISNAMKSEGLKGKLLLVGKTAAKLVYILADSILSRSKGRRLLNKCRLESIRGTLHMILNRERHSAAG
>NZ_CP009279.1|WP_036676609.1|1083192_1084539_+|O-antigen-ligase-family-protein
MTNFEWGSKLNVLPYGMLYLMSALFFGTAVIYQPMIAIAAVLLIILLGISISRPELISYFVLITTAISINFLYDGSMFGMEILSLYKLVIVMLLVPCILVNGLRFRLSHPLWAMVALLVITFGSSIWLPEMTSSIAVKAFIGLSIPFVFLLINWKKNVAELQIKIICMLPLVSVVVGLLLQLAHVHNFLNIEYTGAVRIQGANIPAHLAMLAFMGVAIPFIEVKRNPQQARFFYIMLVLNFFILIGTGTRGPILALGLTVLYYFYDILRQYLKGRTYLLIPLMGAFFLIMVAVFWQLDNFEKRSFERQTDTAVDLSGRSEAWEYFLNKAADSPWSGRGLGAVTVANDGTLYKGFVVPHNEYIRFYFDGGYIGAILLMFSLLAVFILVYRALAPPIKPYYLLFIAAFLIYSFSDNTLSTVQFIIPFCWYLNCLYRSSQPTDSPQKEVIR
>NZ_CP009279.1|WP_036676606.1|1084535_1085309_+|WecB/TagA/CpsF-family-glycosyltransferase
MSQVNMFDVNFDNYDFMDLLDYIDKTIQERNQSYILTCNVDHVIKLRKDKEFQTVYSKAGAVVADGMPLIWASKMLGKPLKQKVSGADLFNRLGNAFEQRKYRLFFLGSAEGVAERAAMNLKTAHPGINVVGCYSPSYGFEHNEEENERIIEMLTECQPDIVFVGVGAPKQEKWIYRHYTSYQAPISIGVGATFDFLSGSVKRAPSFMQKTGFEWFWRLSQEPGRLWKRYLVDDAQFLLLLLKELRKRDKVKEGGLE
>NZ_CP009279.1|WP_052404164.1|1085305_1086784_+|O-antigen-ligase-family-protein
MSVFTPPSLRFIKTAGLIGGTAAAGVSLPLIIGFSSAMLSSSNSLQGAILSAILFPAFLLAILRPKMLVTYTLLIWAVAPELRRIADWSEGVYHSVSLLSLAPLLTGVTLIIPLLKEIHNIQKASTRIMLMFAVALGYGALIGLAKNGMGSVYDLANYIVPLLLLPYFAVTKFKPKDIDRLLTAFANIAVLVAIYGIVQYLTVPPWDVFWMKHADMMSIGNPYPLEIRVFSTLNSPGPAATFLAFALVPMILEKKWRGTLRWIGVLLVVICLLTTLVRAAWLILLVMLLMYIGTSPSKGKWKTLIQLVFVAAALFWVVPKLPGAEGLVARVETLSSVQEDHSYNERLSLWQNMLPMVAANPVGQGIGSVGQGTKLGNDGELGEYGIMDNGVIALLLTFGILGAVFFFGALGAVVKQIFARVISRDQLQPYARLALATWTGAIVSLVSDNGFPGLKGYLIWMLIGLGLSAREITQSRRKGTPYAAVECKISPR
>NZ_CP009279.1|WP_042185176.1|1086749_1088135_+|oligosaccharide-flippase-family-protein
MQQLNAKSLPAKTIWSSFRLFAKSKDNSSAAVKTMFVSVMILLINMLTGVLTARYLGPTGRGEQTAMINWSQFLAFSMSFGIPSALIYNAKKNPEDAGVLYRMALLLGTIFGVIAMIIGIVVLPYWLKSFSPEVVTFAQWSMILCPIIVISQINNAAFQFRGEYKRFNWIRYLVPLLTLTMIGILIALDRMNPFTTAVAYLLPGAPLFIGMTISLLRTYKVKMRGAYQNLKRLFTYGLGSYGNDLLGNFSYYIDQIVIAGLLRPADLGLYVVAVSLSRMVNFFSSSITIVLFPKASELSKEQAVELTFKAFRISTTFTMLGGVVLMLLAPLVIPLMYGKDFNAALTVFRLLLLEVTISGGTIILAQAFMALGKPKIVSMLQGFGLLLVIPMLFLLIPKFGLLGAGIAMLSSAILRFFFIVLNIKYTLKVKLPRLLITREDIQWMKTTMNSYIRKKPMDMNG
>NZ_CP009279.1|WP_042185179.1|1088161_1089019_+|glycosyltransferase-family-2-protein
MDSVKSVVGGQGNYPISAVIIAQDDEVRISKAIQSCRLFADEVIVIDGGSKDGTVQLSESLNCRVYVNPWPGYAKQREFGVERAVHDWVFLIDTDEVVSDELAASILELKPGLKDQSVAYSIYRIGDFMGRWLDRGEYLVRLYNRKAYGIRNSLVHEMPEVSEERTIRLTGTLWHYGYRSINDHVARFNKYTDLEAESAYAKGKRFRVSHLLLRPPARFLQKYFLHGLFKKGMSGFGVSVFWVMYEFMVGFKHYELIRSGKLTQHNAKTSQTEKENKGERSYAVQ
>NZ_CP009279.1|WP_042185181.1|1089005_1090193_+|glycosyltransferase-family-4-protein
MPYSDGLNIMTTGLSWPSLQPGGLNTYFKSVCEQLSSRNRVHALICSQETPATPEELIIHNAGDPKDGIWKRKDAFQRKAADLMGEGSGRIDILYTHFAPYGIGPALEAKKRGIPVVMTFHGPWNEEMKIEGQGIKHRVKTTIAKSIEHRAYKLADKFIVLSETFRDILHKLHGVPLHKIIVIPGAANVERFIPATNRLAIRRSLNLPEGATTVLTVRRLVNRMGLLQLLEAWKQVAERFPNAILLIGGKGPLRGELEEKIADYGLSNKVRLLGYIPDHELASYYQAADMFVVPSQALEGFGLITVEALSSGLPVMATPIGGNKEILQGFRPELLFKSSSSDHMAEGMIHMLSNRKLLPSRDECREHVLERYTWEHVTDQVESVFLQALGEEVTT
>NZ_CP009279.1|WP_042185183.1|1090192_1091332_+|glycosyltransferase-family-4-protein
MLRVAYIDHTAKWSGGEVALFNILTHIGEQIDPLVILAEDGALAERLRENGMDVRIIPLDESIRSRGRNAVNLGAPAAAFKLLAYGRKLAPLLKAEKVDCVHTNSLKSALYGAIAAKIAGVPLIWHIRDHIGAPYLKPIVAKGIRLLSRLLPNGVIANSHSTLNALELPRSKKTLVVYSAFAKAIGNGIGMRDQKDFNVLLVGRLAHWKGQHIVLEAAKSFKNEPRVKFWLAGDALFGEEAYKQELLQKIKNDELTNVSMLGHVDDIQGLMNTADLLIHTSVTPEPFGQVIVEGMAAGLPVIASNEGGPVEIVVQGETGLLIEPGDAAILADSIKWMLDHPEERRRMADNGMKRVKEHFVIENTVKDIVDYYKGLLAGT

Crispr_ID: NZ_CP009279_3

• CRISPR_ID: NZ_CP009279_3
• CRISPR_location: 1607708-1607782
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: DinG

Consensus repeat of NZ_CP009279_3

Consensus_repeat	Method
ATGGGGAAATCCTCCCTATAATTC	CRISPRCasFinder

spacers of NZ_CP009279_3

>3.1|1607732|27|NZ_CP009279|CRISPRCasFinder
TACATTAAAAGCTCATGTGGAGAGATT

CRISPR arrays and Neighbor proteins around NZ_CP009279_3

CRISPR arrays

The CRISPR arrays of NZ_CP009279_3

>merge|NZ_CP009279|3|1607708-1607782|CRISPRCasFinder
ATGGGGAAATCCTCCCTATAATTCTACATTAAAAGCTCATGTGGAGAGATTATAGGGAAATCCTCCCTATAATTC

>NZ_CP009279|3|3|1607708-1607782|CRISPRCasFinder
ATGGGGAAATCCTCCCTATAATTC	TACATTAAAAGCTCATGTGGAGAGATT
ATAGGGAAATCCTCCCTATAATTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042185881.1|1597000_1599019_-|ATP-dependent-DNA-helicase	DinG	COG1199_DinG_CAS-IV-A	gnl|CDD|224120
NZ_CP009279.1|WP_042185889.1|1608174_1610580_-|MMPL-family-transporter	unknown	unknown	gnl|CDD|225272
NZ_CP009279.1|WP_042185898.1|1615175_1616015_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009279.1|WP_042185900.1|1616014_1616896_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP009279.1|WP_042185883.1|1599266_1599713_+|4-vinyl-reductase	unknown	unknown	gnl|CDD|224633
NZ_CP009279.1|WP_042185904.1|1617538_1618237_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187586
NZ_CP009279.1|WP_042185902.1|1617071_1617536_+|lactoylglutathione-lyase	unknown	unknown	gnl|CDD|319912
NZ_CP009279.1|WP_042185906.1|1618434_1619442_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|376439
NZ_CP009279.1|WP_042185892.1|1611483_1613016_-|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_CP009279.1|WP_042185873.1|1588464_1589358_+|ROK-family-protein	unknown	unknown	gnl|CDD|366120
NZ_CP009279.1|WP_042185890.1|1610608_1611226_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP009279.1|WP_042185871.1|1586961_1588443_+|glycoside-hydrolase-family-32-protein	unknown	unknown	gnl|CDD|350134
NZ_CP009279.1|WP_156113071.1|1595577_1596792_+|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|236901
NZ_CP009279.1|WP_042185869.1|1585234_1586845_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270299
NZ_CP009279.1|WP_042185887.1|1603002_1607460_+|1,4-beta-xylanase	unknown	unknown	gnl|CDD|366032
NZ_CP009279.1|WP_042185885.1|1599831_1602486_-|cation-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319781
NZ_CP009279.1|WP_042185875.1|1593496_1594501_+|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_CP009279.1|WP_052404192.1|1589445_1593249_+|DUF1080-domain-containing-protein	unknown	unknown	gnl|CDD|350134
NZ_CP009279.1|WP_042185894.1|1613220_1613802_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379534
NZ_CP009279.1|WP_143764054.1|1613871_1615143_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|224567

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP009279.1|WP_042185881.1|1597000_1599019_-|ATP-dependent-DNA-helicase	DinG	COG1199_DinG_CAS-IV-A	1.4e-82	272.7	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042185881.1|1597000_1599019_-|ATP-dependent-DNA-helicase	gnl|CDD|224120	COG1199, DinG, Rad3-related DNA helicases [Transcription / DNA replication, recombination, and repair].	3.96515e-88
NZ_CP009279.1|WP_042185889.1|1608174_1610580_-|MMPL-family-transporter	gnl|CDD|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	2.73719e-93
NZ_CP009279.1|WP_042185898.1|1615175_1616015_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.12296e-72
NZ_CP009279.1|WP_042185900.1|1616014_1616896_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	4.97279e-71
NZ_CP009279.1|WP_042185883.1|1599266_1599713_+|4-vinyl-reductase	gnl|CDD|224633	COG1719, COG1719, Predicted hydrocarbon binding protein (contains V4R domain) [General function prediction only].	5.00318e-14
NZ_CP009279.1|WP_042185904.1|1617538_1618237_+|SDR-family-oxidoreductase	gnl|CDD|187586	cd05325, carb_red_sniffer_like_SDR_c, carbonyl reductase sniffer-like, classical (c) SDRs. Sniffer is an NADPH-dependent carbonyl reductase of the classical SDR family. Studies in Drosophila melanogaster implicate Sniffer in the prevention of neurodegeneration due to aging and oxidative-stress. This subgroup also includes Rhodococcus sp. AD45 IsoH, which is an NAD-dependent 1-hydroxy-2-glutathionyl-2-methyl-3-butene dehydrogenase involved in isoprene metabolism, Aspergillus nidulans StcE encoded by a gene which is part of a proposed sterigmatocystin biosynthesis gene cluster, Bacillus circulans SANK 72073 BtrF encoded by a gene found in the butirosin biosynthesis gene cluster, and Aspergillus parasiticus nor-1 involved in the biosynthesis of aflatoxins. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.23593e-62
NZ_CP009279.1|WP_042185902.1|1617071_1617536_+|lactoylglutathione-lyase	gnl|CDD|319912	cd07249, MMCE, Methylmalonyl-CoA epimerase (MMCE). MMCE, also called methylmalonyl-CoA racemase (EC 5.1.99.1) interconverts (2R)-methylmalonyl-CoA and (2S)-methylmalonyl-CoA. MMCE has been found in bacteria, archaea, and in animals. In eukaryotes, MMCE is an essential enzyme in a pathway that converts propionyl-CoA to succinyl-CoA, and is important in the breakdown of odd-chain length fatty acids, branched-chain amino acids, and other metabolites. In bacteria, MMCE participates in the reverse pathway for propionate fermentation, glyoxylate regeneration, and the biosynthesis of polyketide antibiotics. MMCE is closely related to glyoxalase I and type I extradiol dioxygenases.	3.16357e-27
NZ_CP009279.1|WP_042185906.1|1618434_1619442_-|iron-ABC-transporter-permease	gnl|CDD|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	2.43207e-78
NZ_CP009279.1|WP_042185892.1|1611483_1613016_-|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].	1.92619e-112
NZ_CP009279.1|WP_042185873.1|1588464_1589358_+|ROK-family-protein	gnl|CDD|366120	pfam00480, ROK, ROK family.	1.67697e-81
NZ_CP009279.1|WP_042185890.1|1610608_1611226_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.63538e-07
NZ_CP009279.1|WP_042185871.1|1586961_1588443_+|glycoside-hydrolase-family-32-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	3.50767e-160
NZ_CP009279.1|WP_156113071.1|1595577_1596792_+|GHKL-domain-containing-protein	gnl|CDD|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	8.93759e-48
NZ_CP009279.1|WP_042185869.1|1585234_1586845_+|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.	0
NZ_CP009279.1|WP_042185887.1|1603002_1607460_+|1,4-beta-xylanase	gnl|CDD|366032	pfam00331, Glyco_hydro_10, Glycosyl hydrolase family 10.	5.93269e-113
NZ_CP009279.1|WP_042185885.1|1599831_1602486_-|cation-translocating-P-type-ATPase	gnl|CDD|319781	cd02089, P-type_ATPase_Ca_prok, prokaryotic P-type Ca(2+)-ATPase similar to Synechococcus elongatus sp. strain PCC 7942 PacL and Listeria monocytogenes LMCA1. Ca(2+) transport ATPase is a plasma membrane protein which pumps Ca(2+) ion out of the cytoplasm. This prokaryotic subfamily includes the Ca(2+)-ATPase Synechococcus elongatus PacL, Listeria monocytogenes Ca(2+)-ATPase 1 (LMCA1) which has a low Ca(2+) affinity and a high pH optimum (pH about 9) and may remove Ca(2+) from the microorganism in environmental conditions when e.g. stressed by high Ca(2+) and alkaline pH, and the Bacillus subtilis putative P-type Ca(2+)-transport ATPase encoded by the yloB gene, which is expressed during sporulation. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP009279.1|WP_042185875.1|1593496_1594501_+|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	1.79027e-14
NZ_CP009279.1|WP_052404192.1|1589445_1593249_+|DUF1080-domain-containing-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	1.16134e-110
NZ_CP009279.1|WP_042185894.1|1613220_1613802_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379534	pfam14278, TetR_C_8, Transcriptional regulator C-terminal region. This domain is a tetracycline repressor, domain 2, or C-terminus.	8.24096e-15
NZ_CP009279.1|WP_143764054.1|1613871_1615143_-|extracellular-solute-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	2.94349e-52

Protein sequences

>NZ_CP009279.1|WP_042185887.1|1603002_1607460_+|1,4-beta-xylanase
MSRMFKQVISILLAAALLIPSSWLAPITEAAAPDAIVPSDSVMVYHETFANGKGIAGQSGSASLTPVTDKAFAGNADGAALYVSNRTNNYDAVDFKFSDMGLENGKTYMVTASVYVDADVTVPSGAQAYLQTINSYGLLASVNYEAGKAITLTKEFTVDTSENTTLRILSDEIGKAVPFYIGDVLITAKKAVTETDKEIYHESFVSGKGLATQSGSANLTAVTGKVFAGNADGAALYVSDRTNDWDAADFTFSDIGLKNGKTYTVTATVYVDPDVTVPSGAQAYIQAIGSYALLASGDYEAGKGITLTKEFIVDTSKDTKLRVQSNAIGKAVPFYIGDVLVTEKVTAEPTPLPTPEPPRDPALPFTTVTFEDQKAGGFEGRAGSETLTITDDENHTDNGSYALKVEGRTSTWHGPSLRVEKYVDKGYEYKISLWVKLIQPASSQLQLSTQVGNGSSANYVQLAPKTISANDGWVQFEGTYRYNNVSSEYLTIYVESSSNSTASFYIDDISFEKTGSGPVGIQKDLIPIKDAYEDHFLIGNAISAEDLEGVRLDLLKMHHNVATAGNAMKPDALQPTKGNFTFTGADELVDKVLHEGMQMHGHVLVWHQQSPAWMNTTSDADNNTIPLGRDEALDNMRTHIKTVMEHFGDKVISWDVVNEAMSDNPSNPTDWKTALRSAPWKSAIGADYVEQAFLAAREVLDANPDWNIKLYYNDYNEDNQNKAQAIYSMVKEINDKYALTHPGKLLIDGVGMQAHYSINTNPENVERSLEKFISLGVEVSITELDIQAGSNYQLSEKLANAQGYLYAQLLNIFRANDEHIKRVTFWGMDDNTSWRASSNPLLFDKNLQAKPAYYGVIDPDTFIEEHEPETVEANHSTAKFAAPVIDGTVDEIWSQTAEMPINRYQTAWQGASGVAKALWDDQNLYVLIQVSDTQLDKSSVNAHEQDSVEIFVDQNNGKTTFYQEDDGQYRVNFDNETSFNPTSIAAGFESATHISGTNYTVEVKIPLHGITPDDDTKLGFDVQINDAKDGSRQSVAAWNDTTGTGYMDTSVYGVLTLKGKSTDTEPTPTPTPTPTNEPTGSSNTGSAVTTPQPVAIANKDGVVTITLEVKSDNGRAIGTISSDNLKKALEQATAAANGKKQIVIEVPKQTDAKVYDIQLPTQSLMGKENFELLLKTENATIQIPSNMLPDLTDHAEQVSIRISKVSADSLSAATRNLIGSHPVIDLSVVSGDKVIPWNNPNAPVTVSIPYTPTAEELSNPDLIVVWYIDDKGNVVPVPNGRYDAATQTVVFQTTHFSIYAVTFVKKNFGDLQNVSWAKQAIDVMAARDVIQGTSVNSFSPADSMKRADFIALLVRALELKGTGKSAALFSDVQKTDYYYDELVIAKELGIATGFEDDTFRPNIEVSRQDMMVLTARALAASGKQIKASGTLNAYLDEASISSYAKDSALLLVKFGVVNGKNDRIAPNDTLTRAEAAVILYRIWKL
>NZ_CP009279.1|WP_042185885.1|1599831_1602486_-|cation-translocating-P-type-ATPase
MEYYRKNVTDSLQEVQSTTNGLTSAEVDKRLERDGYNELKGKKKDPLWKLFLENFKDPMVVVLLIAAIVQIVMGQVMESLIIFLVLILNAVISVIQTRKAESSLDALQQMSAPEAKVLRDGALKTVPARELVRGDIVLLEAGDFVPADGRIIESGSLKINEGMLTGESEAVEKHTDTIAKESPLGDRRNMAFSGSLVVYGRGTLVVTGTALTTEIGKIAELIESAEAKQTPLQRKLETFSKQLGVAIIVLSVLIFAIQAGRVWLSNDTVDTTEAILNALMFAVAVAVAAIPEALSSIVTIVLSVGTNKMAKQHAIIRKLPAVEALGSTSVICTDKTGTLTQNKMTVVDYFLPEGDRDQFNQEPEEWSEEARRLLHIAVLCNDSNINEDGKELGDPTEVALIAFSNSMNKDYKEIRDNFPREAELPFDSDRKLMTTLHTFNGQKAMITKGGPDVLFSLCTHVLLSGQEVPMTPEVLDRFIEANEEFSSRALRVLAYAYKTVPNTVTEVGLEDEQNLVLVGLTAMIDPPREAVYGAIAESKKAGIRTIMITGDHKTTAQAIGRDIGLMTEKEIAVTGQELDAMSDEELDNKLEQIGVYARVSPENKIRIVRAWQRKGKITAMTGDGVNDAPALKQADIGVAMGSGTDVAKDAAAMILTDDNFVSIVNAVSVGRTVFDNIKKAIAYLFSGNLGAIIAILFALIFDWINPFTAIQLLFINLANDSLPAIALGMEKPEPNVMNRNPRELKEGIFAGGMMQAIITRGLLIGIAVIISLYIGLQHSPDMGVAMAFTTLILSRTLQTFAARSNSQTAIEAGFFSNKYVIGAVLVCFAFYGIAVLPGVREIFSIPASFGLSDWLIASGLALGAVILMELTKVIRRAFTPKSAS
>NZ_CP009279.1|WP_042185883.1|1599266_1599713_+|4-vinyl-reductase
MDHFTFTDMKKIKRENLGDAVPLELFRTIRLIGLYQALPMNGKGTTLTIGRKIGEEFGVTSVNELFGLFEQMKIGIPIITHEDDKGMSIAVHDCFCEGLPIMEGKMVCDLEGAIIEGALSKIRGKRVSVREVKCNVHGDECCEYIVKY
>NZ_CP009279.1|WP_042185881.1|1597000_1599019_-|ATP-dependent-DNA-helicase
MSWLSDLYKLQKRELKKDIEPSLVNAIFRMYDRFPRIGLKERIGQQDMSLDIADAYINGRNAMIEAGVGIGKSFAYLIPSLLINQVSRQPIIIATSSIQLSEQIHKDLRFIGSRLGFTSVRSVVGKGMGQYACRYRAADLLQPDDSSSPLSTLAQRIVNYDIDERADIKGGVSDAVWSNVCVNDCKFERCHYKSTCSFYEMRAKINADASDMDFIIVNQDLLIRDLIKKKEGTKGLITERPALIVIDEAHNLEAKVRDARTLEFTYRGTCRILDDTLQILFKQSADNGLLPQFKFLKRCVAHIFKQVEADLLQTAKQDNDRIKVSEITGIPLKRGAQVLKEFSLSLSVLTSKHEREIDNLFEALNGLIDLFDVLAGVQDNYLIWGSNTQREATISICPKGISQFLRYSLFNGKTSVILTSATMCQTGETLEEQYAYLTQSLGYKGDYMERQASPFDYDNHTMLYISKDIPYYNHQNKVGYLEAAYKEMLRLCNLTDGRTLVLFSAKEDMKYIHNKLKSEKLAWAVHVQREGSSQDGVIAEFRGSKGVLLSTGVFWEGVNIEGSDLSQLIIFRLPFPVPSDPVYEYKASLAKDPLNDVFVPDMLLRLRQGTGRLIRSETDLGVLSILDSRLSAAAKKDYRDKALESLPFKKVTEDFRVLEKFVKEKEIQLSVK
>NZ_CP009279.1|WP_156113071.1|1595577_1596792_+|GHKL-domain-containing-protein
MNTKQQRGRMKMSYRANALRSSLTLAVPIILDRHYHSITMKNIESVWFVETHKELLDSTFSTILISMIEALFLDSFGYDQYLSLLEKEGVERGIYTAEIFGDHFDILLEMSKDLNLIAQNMMFKIIEEIEDESTTRLFFYNRLMESNWTGFTGFAKGYLSNKNQQIDNLHEQKIAVMGQMAAGMAHEIRNPLASIKGFAQLVNNRLYEPVIKADELRAYLDITIKEIDALNGLVTDFLVLARKGDSSKNTGVVYNVIEVIHRVNNIVNQLILSDDIILSVEYSLEKVMTYGNASQLEQVILNILKNSIDSFTAFRGRIDITVSTANEANEIILIFKDNGEGIPLDKLNRIFDPFFTTKQKGTGIGLSICKQLIEMYGGQIKVDSEVQVGTSVMVILPWVNDYHI
>NZ_CP009279.1|WP_042185875.1|1593496_1594501_+|ROK-family-protein
MRTANANLMKEINLNNVRQVMKRINTATKPQLAALTKLSVVTVNSLVKELHELGELFEDLTVPSNGGRPAQTYRYNYNFSLGLVIYLKDKEGQVLISATVVNLENEILAKDEHIIPVFERQFFCDIIEHSIALYPSIKVIGIGIPGQVVNGEIKVSSHHELTGSRMIQEIEQQFELPILVENDVNAAISGYCMNQGEEEEQYLLGLYFPNRYPPGMGIYLNGKILKGNQGMSGEIKFLPDMPDWSLEMGKDTFIDTVCRIIQTLNAVLAPDKIVIYQDKVELETWTSAWEAYQLRHPMPIYPQIVMQNTFQDDFEAGLRWLTLKSLEPDLVELH
>NZ_CP009279.1|WP_052404192.1|1589445_1593249_+|DUF1080-domain-containing-protein
MGNKGKVAICFLMATGLVMTSAGIYVANPGTGWAALAEQEVSKRAKEGFSIFESVTNTNTNLTGWQIKGKGNLVDTPEGILLSSDPKENVMAISETVSEDFIYEADVMIKDMQADATLLFRSNEDGWGSYMLQIVPNAGMIRLQDASGDEGKLKEERKVTVKVGEIYHLKVKAEGSSLKVYWDNAYKPVIEVQDNAYRTGKLGLNVWDGSVLFQNIIVSDLKGNLGAVVTNQGQWQPNINGKKGMVVNQSKSQQIYNKQAADFVYEGNISLRPDSVAALAFRSSADGTKGYEAVLTKEGNQVRVSLTKANGTTIASSQHTYPSQTGAKHHVEIKANGNRIQVFLDGYTPAAIDLTDKTYTDGYAGIVVKQGTAYFQDTYVTDASSYYNEKYRPQYHYTPIRGSASDPNGLVYFEGEYHLFHQDGGTWAHSVSKDMLNWKRLPIALPWNDHGHVWSGSAVADLTNASGLFGDSGGKGLIAYYTSYNPDGPNGNQRIGLAYSKDQGRTWEYSKARPMVIENPGDNGGEPGGWDFRDPKVIRDNDNNRWVMVVSGGDHIRFFTSTNLLDWTLTDSWGYGDYVRGGVWECPDLLQLSVDGTSQKKWILMISTGANSKTGGSDAEYFVGHLTAEGKFVNDNPAGKVLRTDFGKEFYASMSFSNMPDHRSVMMAWMTNWDYPFAFPTTHWKGVLSIPREVSLVTTKDGIQLVQSPIKELQSLRSQLYSTANKVVSPSSQNLLKGVTSGAYEIEAEVEIPAGSQVSEFGFNVRVGGSQKTVVGYKPSESQIFVDRSASGLTDFSSLFSTRHEAPMQTENRRIKMRILVDESSVEVFGNNGKVVFSDVIFPDPASRALSFYTNGGNVKVVSLKVNQLGSVWNQESDSATKIMMDTNDRELSKGQSDTLLAMVENGTGNGAQPLKWNSSNKDVVELNVENSSQATIVGKKEGESIITVSTPNGKTSISVLVKVTDGEFHTNLGGWTKDLSAASWVISENGIRGNYLSDANYIAAKQAGDFTYEADMILGKSGGAGSMLFRASEDGRSGYYLNLDPNMKSVRLFYKIEGRFEERQILAKVPMFIQPGQTYKVKIEAKGSHIVVYVDGQKVIDLQDGTFAEGRFGLHVFGGYASYQNVNVSGETPANLTTSSLVNAKLQKSLYTANLANGEAVTLKDANVSTDQKWVIVPTGDDAGSYSIRTTAGQALDLDTGQNKIQLYPYLGYNNQRWILHKNDDGTLSIISAHHRKALEVSADGTTLSLSEFDPTLDRQKWVITN
>NZ_CP009279.1|WP_042185873.1|1588464_1589358_+|ROK-family-protein
MRIGAIEAGGTKFICGIGNENGEIEDQISFPTEHPEVTLPKVIQYFQGKQVEAIGIGSFGPIDIHTDSRAYGYVTTTPKPGWGNYDMLGTLKRNFSVPFGWDTDVNAAAFGEAKWGAAQGLSSCLYYTVGTGVGVGVYSEGKLIHGLVHPEGGHVLTRRHPDDVFPGGCPYHGDCLEGMAAGPAIEARWGKKGHELPMDHLAWEMEAFYIAQSITGAILLNSPQKIILGGGVMQQSQLFPLIRQAVLQNLNGYVSSSTILEHIDEYIVPPGLGQQAGLCGALALGLTALESKISAQL
>NZ_CP009279.1|WP_042185871.1|1586961_1588443_+|glycoside-hydrolase-family-32-protein
MSTIAKQNYRGVYHFSPKEKWMNDPNGMVYFEGEYHLFFQHHPGGMTMGAMHWGHAVSKDLVTWEELPIALAPDELGMIFSGSAVVDWNNTTGFFEGKPGLVAIFTHHLDMPEGKPAIQRQSLAYSKDNGRTWTKYEGNPVLEHDTFIDFRDPKVFWNQDTNQWVMIVACGQTVCLYHSPDLINWTYASEFGNGIGSHDGVWECPDLFPLAIDGDHSNTKWVMLVSIGADPAFVEGSRTQYFTGDFDGEVFTPDEDSIKVRWIDYGRDNYAGVSWSDIPAEDGRRLFIGWMSNWMYANKTPAEEFRGAMTIARELQLESRQGEILLVQKPVQELESARVQVLSVKEATVQEINTLLKEIHLESYEIIAEFTRGKSVGFKVRVGADSQTIIGINGETEELYVDRMASGQHDFHEHFVGHHSAKLEALDESNDLRIFVDRSSVEAFSNGGQAVITDLIFPGLEPKGIAVFAENENDLLISLDIYELTPSAEQDKN
>NZ_CP009279.1|WP_042185869.1|1585234_1586845_+|extracellular-solute-binding-protein
MKRIKKSRVSTKAASVTVLASLMFLSACGGGGGGSAASKEQDASGKVTLNFITQSSPLAPTDPNEKLINKRLEEKTNVHINWKNFTKDVFVEKRNLAVASGDLPDAIFNADYSDYELLKLAKDGAIVPLNDLIENNMPNFKKVLEEAPEYKSMITAPDGNIYAFPWIEELGSGKERIQAVDSMPWINVEWLKKLGLDMPKTTEELKEVLIAFKTKDPNGNGKADEIPLSFINKPGAEDLAFLFASFGLGENPDHAVVSNDGKVIFTAAQEDYKEAVSFINELYKEGLIDIEAYTQDWSTYLAKGKDQKYGLYFSWDKANITGDNDSYEVMPPLAGPDGEVNVTRTNALGLGRGKMVVTSANKNLETTAKWVDQLFDPIQSVQNNWGTYGDEKQQNIFEFDKEKGMLKHLPLEGAAPVELREKTSVGGPLAILDSYYGKYTTMPDDAKSRMDIIKNIMAPKMKAENVMPSVFHSIQELDRLTTIETDLFAYVLRMRTEWYQNGKIEAQWDEYLKELDRLGLQEWLEIKQGGYDRATQ
>NZ_CP009279.1|WP_042185889.1|1608174_1610580_-|MMPL-family-transporter
MSTFLYRLGKSAYTKPWYFLTVWILILGVIGALLGVNGIQSSSEMKIEGTESQKVLDMLVKELPAAAGGQASVAFTAPDGERLDTPERSARILKAINDVYSMDYIINPAELAAQAAAAAGQAAGADPSAAASGQTATADPSAAAGQTDAADPSAAASQTDVSGQATAAAQAAPYGPLIVDGAPVPGVMLSADGSIALFQFQFTVQQTSLPPSVPDNVIKAVTEVEQAGSGITAIPSDSLKSTPSIGSTEAIGVAVAAVVLFITLGSIVAAGLPLITALLGVAISVGGAFALSNIVHMNDITPILAVMIGLAVGIDYSLFIVNRQRRLILDENLSAKEAASRAVGTAGSAVFFAGLTVIIALCGMLVIGIGFLSTMALVAAVSVLITVLLALTLLPALLGLVGERICTAKARSKNVASANKARHGFSHRWANATVKYRWAIIVLVVLVLGTAAIPVTKMELGIPSGASANLDTPARQSYDIISKGFGEGFNGPLLLVAQPNNPSDKISMETLGKLVQELQMHDNVTLVSPMGVNATGDIAIISLIPKTGPTDTKTRDLVQDLRDPASSLASSNDVTLGVTGFTAINIDMSSKLSDAFPVYIGIIVILSLIILLLVFRSVIVPIKATVGFILSVLATFGLTTAVYQWGWLHSLFGFDTGGPLLSFMPILVTGILYGLAMDYQVFLVSSMREAYVHGRRGNDSVVHGYDLASRVVLAAGVIMVSVFAGFIFAPDAMIKQIGFALAFGILIDAFIIRMTLVPAVMAVFGDKAWWLPKWLDRLLPNLDVEGDKLIAMLNAKGEGKK
>NZ_CP009279.1|WP_042185890.1|1610608_1611226_-|TetR/AcrR-family-transcriptional-regulator
MNPKQTLRDKKKEATAYALAKSAFELALELGMDGFIVDDVVQKAGYSRRTFANYFSCKEEAVAAYFISNSSREDKSMLFDNLPPDATPLDALYKLFKLQFTSEFLYQLRQFVSLANQYQSLEPYILSVFRRLQIAAQEVLEQFTHGRYADGYTHLLAGAVYGAFVPILDGRLNVMLPGEAQDEHSDAISFDQYLNSMFTYLRKGF
>NZ_CP009279.1|WP_042185892.1|1611483_1613016_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MIDDLRGWSGVSTKTEVSSSSVKKGPILFIMILGAFLATLNQTVMSVAVPELMHDFNISAATAQWLTTGYMLVNGVLIPITAYLMQRFTTRELFQASMFIFLAGTIVSAIATNFPILLTGRMIQAAGAGIIMPLLTNVILTLFPPAKRGAAMGMVGLAIIFAPAIGPTLAGYILEHYSWETMFYGMIPLTVIVIICGFIYLRNVSERIYPKLDIVGVVLSTIGFGTLLYGFSRAASAGWSSAEVLLSLGLGVLSLGLFTWKQLASQNPLLDLRAFKYSMFSLTTVISIAVTIVMYADMMLLPLYLQNARGFTAMESGLLLLPGALIMGLLMPVTGKLFDRFGAKWLAIIGLLITIATTLSFVNLTDSTSYMYLVYMSTGRRIGMALLLMPIQTLGLNQLPSKLSAHGTAISNTIRQVAGAVGTSLLVTVMTSRTTTHMKDMLASGSTQNGTQEHMIMEASIQGINDSYLVIVGIGILGLLLSFFIKRVGQAPDPEQEPEVKLKKIIAKEA
>NZ_CP009279.1|WP_042185894.1|1613220_1613802_+|TetR/AcrR-family-transcriptional-regulator
MNNTTQRTDPRVLRTRQLLRDAVIELLEEMDIEKISVNRIAERAKINRVTFYLHYRDLPDMLEKMADEMVEDILQVVNNDDNDHESVEEENLRILESLLKHIAENAKFYKVILTSKRSPIFTDRLFNLMAEIISAHQEKKEGAAEHSKMPIQKDIAVWYGSAALIGTVISWLRDDMPYTPVYLARQISMLRAN
>NZ_CP009279.1|WP_143764054.1|1613871_1615143_-|extracellular-solute-binding-protein
MNMRTKRGILLACSLLLAALTAGCGRGSDNANGVKTVHIYQFKVEISEALASLKTEFEKEHPDIKLEVQSVGGGTDYGASLRAKFSSGDEPDIFTIGGNNERDMWMEYLEDLSGEAWAKDVKPLAAEQMTADGKLYGMPMNLEGYGFIYNKDLFKKAGITEKPLTLTALREASEKLKAAGITPFANGYQEWFVLGNHNVNVAFAQQPDPEAFIAGLTDGTKTFAGDPVFSKWIDLLDLTVEYGNKNPLSTDYNTQVTMVASGEAAMMQQGNWTQGQIDGIDPNLNLGILPMPIDDTPEDNDKLYVGVPSNWVINKNSPVKEEAKVFLDWLVTSETGKKYITKEFQFIPALDSIKGTEEDLGALGAEVLAYTDKDQALTWNWTRLPNGMPQELSSSIQGYLGGKLTKEGMLKEFQVNWDNLSVQ
>NZ_CP009279.1|WP_042185898.1|1615175_1616015_-|carbohydrate-ABC-transporter-permease
METTAKKFNVSLLLVEVIVILLGLLFLVPFYFLLANSVKSYSEILSDSAALPSVFQWSNYAEAWKAINFPRAFLNSFIITVISNILLAFLCSMCAYKMVRNNSLYNRILYIALVAAMVIPFQAIMIPLVQVVSGLGVMDSTTGLILAYLGFGAPMTVFLFHGFVKSVPLDIEEASRVDGNSPYGTFFRIVLPLMQPIIVTVIILNTLWIWNDYLMPSLILQDPVLRTIPIATYSFFGQYTKQWDLALPGLVLGITPVVIFFLAMQKYIIEGIAQGSVKG
>NZ_CP009279.1|WP_042185900.1|1616014_1616896_-|sugar-ABC-transporter-permease
MDHRKRSRLMQQFVFVGPTSLFFFMIVLIPFFLGLYYSFTSWNGISRDVEWTGLRNYLHIFTKDPSFLHSFWFTAKFTFFGLILTNLLGFALAYVLTRKLFTRNVLRTVFFVPHVIGGLLLGFIWQFIFVRGFSSIGQATGWSFFNLPWLGTGGTAFWAIVIVFVWQNAGYLMVIYISAINNVPKSLIEASKVDGAGRFQALRHVTIPLVMPAVTVCLFLSISWSFKLFDLNLSLTKGGPFKATESVALNIYNEAYTISRFGMGSAKAMIFFVIVAVISLLQVRATKKREVEL
>NZ_CP009279.1|WP_042185902.1|1617071_1617536_+|lactoylglutathione-lyase
MSGLLGNFVTQIGILVNDVEKVSTAYAEFFGLKKPEIIVTDTEDIAQTRHNGVATQARAKLAFFDMGSLQLELIEPDHEPSTWRDYLNEHGEGPHHIAFVVEGMKEKIMLLEGKGFPLQQKGEYTGGRYAYMDTFKELKVIVELLENDKDNGEE
>NZ_CP009279.1|WP_042185904.1|1617538_1618237_+|SDR-family-oxidoreductase
MNIIITGAGRGLGYELAAEALKRGYGVIAGVRRPDQEQTALSKLAETYGEKLTIAAMDVTDEAGIAALAASLQEQGRTLGAIINNAAVLNARDTSIEALDFQDMLITMDINLYGPIRVVKHFLPLLTEPECSIINISSEAGSITNAYPNDYPYGISKAALNMFTQQLHVYVKERGIQVLSVHPGWMQTDMGGAEAPTNPNQSAEGILDLIEKRTTPEGHFMFVDYTGKDMKI
>NZ_CP009279.1|WP_042185906.1|1618434_1619442_-|iron-ABC-transporter-permease
MISSAPVRKQRIILCVCTGLILLTAIVSMGIGYSSLSFDRLLPVLFGHGTFKEDFVLFSVRLPRILITLLAGMALALSGSILQSVTRNDLADPGIIGINSGAGVAVAVFFLFFPVSAGSFIYALPLVAFIGALLTAALIYLFSYSRTKGLDPVRLVLVGVGFSLALSGVMIVIISSADRAKVDFIAKWIAGNIWGTDWPFIWALLPWLILLVPFTLYKSQRLNLLSLSEVSAIGVGLNLERERIVLILTAVAASASAVSVTGGIAFIGLMAPHIAKSLVGPRNQMFIPVAVLLGGWLLLIADTVGRNLVDPDGIPAGIMVSLIGVPYFAYLLLKK

Crispr_ID: NZ_CP009279_4

• CRISPR_ID: NZ_CP009279_4
• CRISPR_location: 4855850-4855936
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_4

Consensus_repeat	Method
AAGTTTTGTTAGCATAGCCTTCA	CRISPRCasFinder

spacers of NZ_CP009279_4

>4.1|4855873|41|NZ_CP009279|CRISPRCasFinder
GAGAATTTCTTCGTACAAAACTAGCTTCGTAAGCACCCGCT

CRISPR arrays and Neighbor proteins around NZ_CP009279_4

CRISPR arrays

The CRISPR arrays of NZ_CP009279_4

>merge|NZ_CP009279|4|4855850-4855936|CRISPRCasFinder
AAGTTTTGTTAGCATAGCCTTCAGAGAATTTCTTCGTACAAAACTAGCTTCGTAAGCACCCGCTAAGTTTTGTTAGCATAACCTTCA

>NZ_CP009279|4|4|4855850-4855936|CRISPRCasFinder
AAGTTTTGTTAGCATAGCCTTCA	GAGAATTTCTTCGTACAAAACTAGCTTCGTAAGCACCCGCT
AAGTTTTGTTAGCATAACCTTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042190455.1|4851357_4852701_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	unknown	unknown	gnl|CDD|236307
NZ_CP009279.1|WP_042190451.1|4849212_4849665_-|transcription-antitermination-factor-NusB	unknown	unknown	gnl|CDD|273891
NZ_CP009279.1|WP_081382878.1|4859998_4860865_+|YitT-family-protein	unknown	unknown	gnl|CDD|224203
NZ_CP009279.1|WP_042132343.1|4850826_4851243_-|Asp23/Gls24-family-envelope-stress-response-protein	unknown	unknown	gnl|CDD|377129
NZ_CP009279.1|WP_042129810.1|4848209_4849067_-|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase-FolD	unknown	unknown	gnl|CDD|184560
NZ_CP009279.1|WP_042190466.1|4857837_4858356_-|stage-III-sporulation-protein-AB	unknown	unknown	gnl|CDD|181372
NZ_CP009279.1|WP_042190468.1|4858348_4859350_-|stage-III-sporulation-protein-AA	unknown	unknown	gnl|CDD|274324
NZ_CP009279.1|WP_042190475.1|4863121_4864192_-|aminopeptidase-P-family-protein	unknown	unknown	gnl|CDD|223085
NZ_CP009279.1|WP_042129828.1|4857223_4857613_-|stage-III-sporulation-protein-AD	unknown	unknown	gnl|CDD|131896
NZ_CP009279.1|WP_042190470.1|4860961_4862215_-|aspartate-kinase	unknown	unknown	gnl|CDD|235843
NZ_CP009279.1|WP_042190464.1|4855939_4857181_-|stage-III-sporulation-protein-AE	unknown	unknown	gnl|CDD|213743
NZ_CP009279.1|WP_036683194.1|4859432_4859675_-|YqhV-family-protein	unknown	unknown	gnl|CDD|378514
NZ_CP009279.1|WP_052404383.1|4855073_4855835_-|stage-III-sporulation-protein-AF	unknown	unknown	gnl|CDD|378212
NZ_CP009279.1|WP_081382879.1|4854391_4855051_-|stage-III-sporulation-protein-AG	unknown	unknown	gnl|CDD|274319
NZ_CP009279.1|WP_042190473.1|4862517_4863075_-|elongation-factor-P	unknown	unknown	gnl|CDD|234788
NZ_CP009279.1|WP_042190453.1|4849963_4850197_-|DUF2273-domain-containing-protein	unknown	unknown	gnl|CDD|378362
NZ_CP009279.1|WP_036682849.1|4857620_4857824_-|stage-III-sporulation-protein-AC	unknown	unknown	gnl|CDD|131895
NZ_CP009279.1|WP_042190460.1|4853412_4854324_-|hypothetical-protein	unknown	unknown	gnl|CDD|378918
NZ_CP009279.1|WP_042190457.1|4852755_4853265_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl|CDD|235777
NZ_CP009279.1|WP_042129814.1|4850212_4850752_-|alkaline-shock-response-membrane-anchor-protein-AmaP	unknown	unknown	gnl|CDD|380217

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042190455.1|4851357_4852701_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	gnl|CDD|236307	PRK08591, PRK08591, acetyl-CoA carboxylase biotin carboxylase subunit; Validated.	0
NZ_CP009279.1|WP_042190451.1|4849212_4849665_-|transcription-antitermination-factor-NusB	gnl|CDD|273891	TIGR01951, nusB, transcription antitermination factor NusB. A transcription antitermination complex active in many bacteria was designated N-utilization substance (Nus) in E. coli because of its interaction with phage lambda protein N. This model represents NusB. Other components are NusA and NusG. NusE is, in fact, ribosomal protein S10. [Transcription, Transcription factors].	8.73646e-49
NZ_CP009279.1|WP_081382878.1|4859998_4860865_+|YitT-family-protein	gnl|CDD|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	1.09981e-62
NZ_CP009279.1|WP_042132343.1|4850826_4851243_-|Asp23/Gls24-family-envelope-stress-response-protein	gnl|CDD|377129	pfam03780, Asp23, Asp23 family, cell envelope-related function. The alkaline shock protein Asp23 was identified as an alkaline shock protein that was expressed in a sigmaB-dependent manner in Staphylococcus aureus. Following an alkaline shock Asp23 accumulates in the soluble protein fraction of the S. aureus cell. Asp23 is one of the most abundant proteins in the cytosolic protein fraction of stationary S. aureus cells, with a copy-number of >25000 per cell. A second Asp23-family protein, AmaP, which is encoded within the asp23-operon, is required to localize Asp23 to the cell membrane. The overall function for the family is thus a cell envelope-related one in Gram-positive bacteria.	2.13343e-40
NZ_CP009279.1|WP_042129810.1|4848209_4849067_-|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase-FolD	gnl|CDD|184560	PRK14190, PRK14190, bifunctional 5,10-methylene-tetrahydrofolate dehydrogenase/ 5,10-methylene-tetrahydrofolate cyclohydrolase; Provisional.	1.93056e-157
NZ_CP009279.1|WP_042190466.1|4857837_4858356_-|stage-III-sporulation-protein-AB	gnl|CDD|181372	PRK08307, PRK08307, stage III sporulation protein SpoAB; Provisional.	2.21573e-62
NZ_CP009279.1|WP_042190468.1|4858348_4859350_-|stage-III-sporulation-protein-AA	gnl|CDD|274324	TIGR02858, Stage_III_sporulation_protein_AA, stage III sporulation protein AA. Members of this protein are the stage III sporulation protein AA, encoded by one of several genes in the spoIIIA locus. It seems that this protein is found in a species if and only if that species is capable of endospore formation. [Cellular processes, Sporulation and germination].	2.58967e-128
NZ_CP009279.1|WP_042190475.1|4863121_4864192_-|aminopeptidase-P-family-protein	gnl|CDD|223085	COG0006, PepP, Xaa-Pro aminopeptidase [Amino acid transport and metabolism].	1.44287e-118
NZ_CP009279.1|WP_042129828.1|4857223_4857613_-|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].	2.20467e-24
NZ_CP009279.1|WP_042190470.1|4860961_4862215_-|aspartate-kinase	gnl|CDD|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	0
NZ_CP009279.1|WP_042190464.1|4855939_4857181_-|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].	1.27853e-119
NZ_CP009279.1|WP_036683194.1|4859432_4859675_-|YqhV-family-protein	gnl|CDD|378514	pfam10942, DUF2619, Protein of unknown function (DUF2619). This bacterial family of proteins has no known function.	1.98605e-23
NZ_CP009279.1|WP_052404383.1|4855073_4855835_-|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.	2.1954e-29
NZ_CP009279.1|WP_081382879.1|4854391_4855051_-|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].	4.60316e-49
NZ_CP009279.1|WP_042190473.1|4862517_4863075_-|elongation-factor-P	gnl|CDD|234788	PRK00529, PRK00529, elongation factor P; Validated.	2.8478e-106
NZ_CP009279.1|WP_042190453.1|4849963_4850197_-|DUF2273-domain-containing-protein	gnl|CDD|378362	pfam10031, DUF2273, Small integral membrane protein (DUF2273). Members of this family of hypothetical bacterial proteins have no known function.	4.64884e-09
NZ_CP009279.1|WP_036682849.1|4857620_4857824_-|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].	4.38859e-16
NZ_CP009279.1|WP_042190460.1|4853412_4854324_-|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.	1.60381e-20
NZ_CP009279.1|WP_042190457.1|4852755_4853265_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl|CDD|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	7.09765e-53
NZ_CP009279.1|WP_042129814.1|4850212_4850752_-|alkaline-shock-response-membrane-anchor-protein-AmaP	gnl|CDD|380217	NF033218, anchor_AmaP, alkaline shock response membrane anchor protein AmaP. The founding member of this family, AmaP (Asp23 membrane anchoring protein), is related to Asp23 through part of its length, but includes a highly hydrophobic N-terminal region that should make it an integral membrane protein. Asp23 (alkaline shock protein of 23 kDa), described in PMID:7864904, is a cytosolic protein in Staphylococcus aureus, strongly induced by a pH shift from 7 to 10, and also recruited to the membrane. AmaP appears to be the partner protein with an integral membrane segment and the ability to anchor Asp23 to the membrane. This model was built to identify full-length homologs of AmaP, while excluding Asp23. Some but not all members of this family score above the cutoffs of Pfam model version PF03780.11, but full-length homologs of Asp23 score considerably higher. Asp23 family members previously were known as DUF322.	4.78003e-28

Protein sequences

>NZ_CP009279.1|WP_052404383.1|4855073_4855835_-|stage-III-sporulation-protein-AF
MSWLGDWLREIILVVLLASFVELLLPSKSMERYARLVLSLLILLTMLSPIVSLLKGDAIAELSIAMGRQEKEGGLFTGGGSGDPSLEKILADGQKLAQGRQDQSLKLAAEEVAEQMREQIISETGKRGVNVTVTLGMGKSGGSGNEDIPVISAVKVSMSQATANSIGASGNSSAAAAPPIAIAPVEPVEVKIGTNPESGSASADEPKAVNGNVTENNTTSSETESIVKMLEQKWDLDPEVIQVDGGVVNNVKL
>NZ_CP009279.1|WP_081382879.1|4854391_4855051_-|stage-III-sporulation-protein-AG
MLGGIGVGNWLKKLEQWAGGGAGSPKRSHTFRWLIILGLLGAAIMLFNSFVNVKKIDNENTGREPPLNQSSQTALVQSDPGATNSFESIEQTLENRTKEILEKIVGVGTVDIMVTVESTEEIVVVRNMNDSQQLSEETDASGGKRHTTQYTRDGEIVTYSQSGDETPIVTKRIKPQVRGVLVVAKGAENKVVRGLIEQAIEKGLNVPIQRISVVPRKQE
>NZ_CP009279.1|WP_042190460.1|4853412_4854324_-|hypothetical-protein
MNGKRQTIWLVSMLSLMVVLSAYYLFTEDSGASVPKDTAGTMQVDSLKKDTANAALPTVGDKGIVVNEVVNQGDVVADGGVVDNASGTTATDDSAATATTDDSATTAVKDDSSKAADSGNSEKASTDTAAKDSSKTSDTATKDTAAKDTVTKDTAAKDTAATTTSKTPAKNDKEILDEVASQSVSASSMFTNYLYEREQKNLKSQQDLLALINDMEKTPADNAVAQEQLLNLEEKESKITGIEEQLQQKYGEAIVKEEAGDSYKVVVLSDKLDVKQAVSIVDLVMKELSVSQDKVSVQYVSEK
>NZ_CP009279.1|WP_042190457.1|4852755_4853265_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MFKLSEIKELIKLLDQTSSVHELEIESEGMKLAIRKPDRPEADGTAVQATPYNAYPFTPAPQPQSVQQVSYPVISEVPPAQQPQAVAEGKLHKIVSPMVGTFYSAASPEMPSFVNVGDRVGEKTTVCIIEAMKLMNELEAEIKGEIVSVLAENGQLVEYGQPLFLVKPE
>NZ_CP009279.1|WP_042190455.1|4851357_4852701_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit
MNIQKVLIANRGEIAVRIIRACRELGISTVAVYSEPDRDSLHVRLADEAYCIGPMPSKDSYLNFTNIMSVATLTECDAIHPGYGFLAENADFAEICESCNIIFIGPSPDAINRMGDKAVAKETMKLAGVPIIPGSDGLVGDVEEAVMLGRDIGYPIIIKATAGGGGKGIRIAEDEESLVKQITAAQQEAQKAFGNAGVYLEKYLTGMKHVEIQIIADKHGNVVHLGERDCSVQRRRQKLIEEAPCSVLTPDIREAMGNAAVRAALAVNYSGAGTLEFLLGPDGQFYFMEMNTRIQVEHPVTEMVTGVDLIKEMISVAEGNPLSFTQEDIVINGWSIECRINAEDPERNFMPSPGKIGFYLPPGGLGVRVDSAAYPGYTISPFYDSMIAKLIVWAPTRQEAIAKMKRALAEFAVEGIHTTIPFHQKLLEHPVFLDGNFDIKFLEEYEI
>NZ_CP009279.1|WP_042132343.1|4850826_4851243_-|Asp23/Gls24-family-envelope-stress-response-protein
MSTLPTEYERTEIGEIQIAPEVIEVIAGLATVEVKGVAGMSGGFAGGIVELLGRKNLSKGVKVEVGQREAAVDVSVIIEYGNRLPEVAAEIQRNVKRSIETMTGLTVVEVNVHIHDVQFKNNNTVDKNEEAETVLRVK
>NZ_CP009279.1|WP_042129814.1|4850212_4850752_-|alkaline-shock-response-membrane-anchor-protein-AmaP
MAKILDRLLLFVYSLSIGILSVIAILLLSGAIPKTLEIENGPAAYITAIVVAVVLFLLSIRFFYISLRRDRASLPSVDQRTEYGDIQISVETIENLSLKAAGKVKGIRDLKSRIRVSQAGLEITIRAVVDGEHSLPLLTTEVQRQVHDFVQETTGIPVADVSVYIANLTQSPSFKSRVE
>NZ_CP009279.1|WP_042190453.1|4849963_4850197_-|DUF2273-domain-containing-protein
MSWKEVWESHGGRIAGVTFGIGLGLIYLICGFWDMLFFALVVFIGYTFGKRKDNAEAPLFQWQELITRLSGRWRPFK
>NZ_CP009279.1|WP_042190451.1|4849212_4849665_-|transcription-antitermination-factor-NusB
MKRRIAREIIVQSLYQMEMNDVESAEAVEMLLEEASEENETERVITDEIQLKHYVVEHVNGVWEHKVAIDDMLEHYLKGWQMSRLSRVDRQILRLAAYEMVFANDVPAKVAVNEAIDLAKHFGTDDSGKFVNGVLGKMIQEIDTIKADHS
>NZ_CP009279.1|WP_042129810.1|4848209_4849067_-|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase-FolD
MTAAIISGKQVSEEIRIGIAQEVAELAKRGVKPGLAVILVGEDPGSQVYVRNKEKSCISLGFHSEVHKLDESTTQEELLALVAQLNGRDDIDGILVQLPLPKHIEEKAVIDAISVEKDVDGFHPVNVGNLVIGADSLLPCTPAGVIELIKRTGTGMAGKHAVVIGRSNIVGKPVSLLLQRENATVTMCHSRTANMQEISRQADILVVAIGRANFIDASYVKPGAVVIDVGMNRLDNGKLAGDVDYDSAKEVAGYITPVPGGVGPMTITMLMSNTLIAAKRRHGLE
>NZ_CP009279.1|WP_042190464.1|4855939_4857181_-|stage-III-sporulation-protein-AE
MQKCSVFRPPKLKIILLLLPCFFILWFAGTAQVAIASPATPAPGSGNSSPVDQWVKGQVNNLPTDKVESYWDQLMKDYGGFFPDGATPSLMDMLLPGDKGLSLQGVLSGLLGFMWHEVLYNGRLLVTIVMVSVLSMILETLQTAFERKTVSKVAYTLCYMVVLVIAVNSFNIAIGYAKDAIDRMIDFMMAMIPLLFALLASMGNIVTVSVTHPLIVFMIHTVGTLIHTIVFPLLFFSAVLHLVSALSEKYKLTQLANLLRNIGAGLLGVLLTVFLGVISVRGITSSVTDGVTIRAAKYITGNFVPVIGKMFADATDTVISASLLVKNAIGLSGVIIILFLCAFPAIKILVLALIYNVAAAVMQPLGETPIVVCLQTIGKSMVYVFAALAAVSLMFFMAVTIMLTAGNLTVMMR
>NZ_CP009279.1|WP_042129828.1|4857223_4857613_-|stage-III-sporulation-protein-AD
MEIIQVVGIGLISTILILVLKEQKPMFAFLLATATGILIFLFLIGKIGMILSTLERVAESSGMEMIYLKTVFKIIGISYIAEFGAQIVRDAGQESIASKIELAGKVLIMVLAVPIISIIIETVMKLLPA
>NZ_CP009279.1|WP_036682849.1|4857620_4857824_-|stage-III-sporulation-protein-AC
MNIEVNAIFQIAGIGIIIAMIHTVLKQMGKEDFAHWVTVIGFVVVLFMVIRMLDGLLQEIKTIFLFQ
>NZ_CP009279.1|WP_042190466.1|4857837_4858356_-|stage-III-sporulation-protein-AB
MLKLFGAVLIVLAGTLAGLQFAKQYADRPRHIRGLIAALQRLETEIMYGFTPLPEAMRRIGIQSKEPLKTLFIKTAEEMSPPHDRSAQDAIQRAMDSHWKSTALKGTEKEILRQLSCTLGTSDRSNQSTHIALALQQLKQEESVAREDQGKYEKLSKSLGLLLGALIVILIF
>NZ_CP009279.1|WP_042190468.1|4858348_4859350_-|stage-III-sporulation-protein-AA
MADDWLQLFPEKVRALLKCLPLPLLGMVEEIRVREGRPLEINYSGKYHFLRANGSVTQRPEEAYRPDREDTHRLLDLISNHSLYTMEEELRKGFITIPGGHRIGLAGRTVLSGGGVEHLRDITSFNVRIAREVPGVADKVLPYLLDKGGQRMMHTLILSPPQHGKTTLLRDIARQISLGDLGKREGGRPGMKVGIVDERSEIAGSRRGIPAFDVGPRTDILDGCPKAEGMMMMIRSLSPDVLIADEIGRPEDAEAVTEALHAGISVVASAHGKEVIELARRPGLGGLLEQKMFERYVILHRSEAGLSFRVLDGQKRGLLLISPGDRLGGDLHA
>NZ_CP009279.1|WP_036683194.1|4859432_4859675_-|YqhV-family-protein
MATLRLFSGSAEIIAALIMLRLNQVDKALAVNSGLALVGPTILILTTAIGLTGMAQQLSWSKLGWVGCGVAFLLIGILKK
>NZ_CP009279.1|WP_081382878.1|4859998_4860865_+|YitT-family-protein
MQVRSYGLPQNMRTVVRPLKEVAIIIFSAFLIASGMRLFLIPHQLLSGGVAGVASVVGYLTDPKYISKLYFVINLPLIVWGFIAVGKKYILLSLLSVVATTWFITIIPEVQMTKDPILASIFGGVIIAGGVGFSLRTGGSSGGFDILGSIISRKRDIPMGNIMFLMDGLVILSLGFFKSWDSALYAMLCIFVKSRVVDMIHIRHVKLTCFIVTKEREMMLTRLRELPHGITVVNAEGGYSHEGNTMLMTVTTRYELANLRRTILEADPSSFVNVVETVEIQGRFKRLG
>NZ_CP009279.1|WP_042190470.1|4860961_4862215_-|aspartate-kinase
MSLYVMKFGGSSVGDTERMKRVAKRIADKQDEGHRCVVVVSAMGDTTDDLIDTAKQLNGQPPAREMDMLMTTGEQISVALLSIALHGIGRNAVSYTGWQAGFRTDETHGRARINEIDPRRVLASLEREQIVIVAGFQGMTVDGEITTLGRGGSDTTAVALAAAIQADVCEIYTDVDGIYSTDPRIVKTARKLKEISYDEMLELANLGAAVLHPRAVEYAKRHQVKLVVRSSFNHNEGTVVKEETSMEQGIVVSGIAFDKNVARVSILGVPDVPGVLAQVFGKLAEEGVNVDIIVQSGVQNEQADFSFTVSLDELDRAKEVIKEIHKTLPYREVTSEDNLVKVSIVGAGMVSHPGVAAQMFDVLSQEGVSIKMVSTSEIKVSCVIESGNLPSIIQALHTAYNLDTTEQAFVGGPKDRR
>NZ_CP009279.1|WP_042190473.1|4862517_4863075_-|elongation-factor-P
MISVNDFKTGLTVEVEGDIFTVIDFQHVKPGKGAAFVRSKLKNLRNGNTVERTFRAGETIGRAIIENRGVQYLYASGSDHVFMDNETYDQFELSEKQLEWELNFLKENMTVNIVSYKGEILGINLPTSVELKVVETEPGVKGNTAQGATKSAKLETGHSVQVPLFINEEDILLVDTREGKYISRA
>NZ_CP009279.1|WP_042190475.1|4863121_4864192_-|aminopeptidase-P-family-protein
MGNKRVSKLRKVLQDQGLDAMLITSGYNRRYLSGFTGSSGYVLVTSDDCYLLTDFRYMTQAADQAMGVKVVEHATKFIDTVRELLPSGKEVRIGFEQDDVSFSAYTSYAEALKPAVLVPISKAVEDLRMFKDEEELAVMQRAADLADATFSHILNVIKPGMTERDVDLEMEFYMRTHGATSSSFDTIVASGERSSMPHGVASSRVIQGNEFITLDFGALLDGYCSDVTRTIALGAPDPKLKEIYDIVLEAQLYTLAHIMPGMTGRECDALARDIIASYGYGEHFGHSTGHGLGMEVHEWPRLSKLSDDIMQPGMVVTVEPGIYLPGIGGVRIEDDIVITESGISLLTHSSKEYTVL

Crispr_ID: NZ_CP009279_5

• CRISPR_ID: NZ_CP009279_5
• CRISPR_location: 5586358-5586448
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_5

Consensus_repeat	Method
CGTAGTAAAACTCGCTTCGAAAGCAT	CRISPRCasFinder

spacers of NZ_CP009279_5

>5.1|5586384|39|NZ_CP009279|CRISPRCasFinder
CCACTTAGTTTTACGAAGCGTTGCTCAAGTTTCTTACTC

CRISPR arrays and Neighbor proteins around NZ_CP009279_5

CRISPR arrays

The CRISPR arrays of NZ_CP009279_5

>merge|NZ_CP009279|5|5586358-5586448|CRISPRCasFinder
CGTAGTAAAACTCGCTTCGAAAGCATCCACTTAGTTTTACGAAGCGTTGCTCAAGTTTCTTACTCCGTAGTAAAACTCGCTTCGGAAGCAT

>NZ_CP009279|5|5|5586358-5586448|CRISPRCasFinder
CGTAGTAAAACTCGCTTCGAAAGCAT	CCACTTAGTTTTACGAAGCGTTGCTCAAGTTTCTTACTC
CGTAGTAAAACTCGCTTCGGAAGCAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_081383034.1|5597230_5597491_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_052404406.1|5584807_5586271_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|379337
NZ_CP009279.1|WP_042191466.1|5577144_5578185_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_CP009279.1|WP_042191479.1|5582047_5583034_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|367154
NZ_CP009279.1|WP_042191483.1|5584259_5584751_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191487.1|5589350_5590112_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|226425
NZ_CP009279.1|WP_081951201.1|5578181_5578964_-|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_CP009279.1|WP_042191497.1|5596075_5596603_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP009279.1|WP_042194464.1|5586652_5587768_-|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_CP009279.1|WP_042191499.1|5596809_5597226_-|hypothetical-protein	unknown	unknown	gnl|CDD|235562
NZ_CP009279.1|WP_042191481.1|5583023_5584118_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl|CDD|340819
NZ_CP009279.1|WP_042191472.1|5579518_5580235_-|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_CP009279.1|WP_042191493.1|5593772_5595110_-|5'-deoxyadenosine-deaminase	unknown	unknown	gnl|CDD|180895
NZ_CP009279.1|WP_081951202.1|5587819_5588836_-|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_CP009279.1|WP_042191470.1|5578935_5579511_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_CP009279.1|WP_042191491.1|5591683_5593576_-|LTA-synthase-family-protein	unknown	unknown	gnl|CDD|293739
NZ_CP009279.1|WP_042191474.1|5580231_5581215_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|366597
NZ_CP009279.1|WP_042191495.1|5595534_5596014_+|hypothetical-protein	unknown	unknown	gnl|CDD|374812
NZ_CP009279.1|WP_042191477.1|5581211_5582051_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187564
NZ_CP009279.1|WP_042191488.1|5590259_5591675_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_052404406.1|5584807_5586271_-|glycosyltransferase-family-4-protein	gnl|CDD|379337	pfam13692, Glyco_trans_1_4, Glycosyl transferases group 1.	1.65392e-28
NZ_CP009279.1|WP_042191466.1|5577144_5578185_-|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.	6.89359e-31
NZ_CP009279.1|WP_042191479.1|5582047_5583034_-|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).	1.6206e-124
NZ_CP009279.1|WP_042191487.1|5589350_5590112_+|AAA-family-ATPase	gnl|CDD|226425	COG3910, COG3910, Predicted ATPase [General function prediction only].	1.31905e-95
NZ_CP009279.1|WP_081951201.1|5578181_5578964_-|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.	6.17726e-36
NZ_CP009279.1|WP_042191499.1|5596809_5597226_-|hypothetical-protein	gnl|CDD|235562	PRK05687, fliH, flagellar assembly protein FliH.	0.000220201
NZ_CP009279.1|WP_042194464.1|5586652_5587768_-|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	2.24942e-34
NZ_CP009279.1|WP_042191481.1|5583023_5584118_-|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.	4.13881e-118
NZ_CP009279.1|WP_042191472.1|5579518_5580235_-|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.	4.2687e-40
NZ_CP009279.1|WP_042191493.1|5593772_5595110_-|5'-deoxyadenosine-deaminase	gnl|CDD|180895	PRK07228, PRK07228, 5'-deoxyadenosine deaminase.	0
NZ_CP009279.1|WP_081951202.1|5587819_5588836_-|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	1.01085e-30
NZ_CP009279.1|WP_042191470.1|5578935_5579511_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	4.21986e-07
NZ_CP009279.1|WP_042191491.1|5591683_5593576_-|LTA-synthase-family-protein	gnl|CDD|293739	cd16015, LTA_synthase, Lipoteichoic acid synthase like. Lipoteichoic acid (LTA) is an important cell wall polymer found in Gram-positive bacteria. It may contain long chains of ribitol or glycerol phosphate. LTA synthase catalyzes the reaction to extend the polymer by the repeated addition of glycerolphosphate (GroP) subunits to the end of the growing chain.	4.04365e-88
NZ_CP009279.1|WP_042191474.1|5580231_5581215_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|366597	pfam01370, Epimerase, NAD dependent epimerase/dehydratase family. This family of proteins utilize NAD as a cofactor. The proteins in this family use nucleotide-sugar substrates for a variety of chemical reactions.	1.55867e-44
NZ_CP009279.1|WP_042191495.1|5595534_5596014_+|hypothetical-protein	gnl|CDD|374812	pfam16800, Endopep_inhib, IseA DL-endopeptidase inhibitor. This domain functions as a DL-endopeptidase inhibitor.	2.77593e-05
NZ_CP009279.1|WP_042191477.1|5581211_5582051_-|SDR-family-oxidoreductase	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.	9.15251e-65
NZ_CP009279.1|WP_042191497.1|5596075_5596603_-|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.	2.17363e-15

Protein sequences

>NZ_CP009279.1|WP_052404406.1|5584807_5586271_-|glycosyltransferase-family-4-protein
MADKATIVLFSHVSNTRSITGAEKLLLFFAQELSPYFNCIIVAPQDGKLTAQARSFGISVQLLSIPLLYGMYTPYAGLEADARKFQESREYHELTDWLTSLRPAFIITSTCVHALPAMAAKSLGIPVVWKISETITDNEYTPISVGLIHRNSDEILAISQTAAACFPEEVRAEKVIQLPPSWNDKEMMIEAWSKLRGERRRELKIKPQEQLVGYISSFINKEKGLEHFVKMAVLVYAVHPSAKFVVIGSAGDKSYYDRCVRKVKLEGLYTRFKFVGYAECLPSAYCAMDVLVVPSLIREGFGMTALEGMAFGKPVVAYDSGGLREILHSAGCGENLVPASDISALAERVNVMLSQPGLAITIGAQARERVDAVYGPAAYRSRLQGLAEMWSLRYCSAPPVREADSVVEPPAVLPELPAASPALPRSKGLPSRVARKRRGKARARRRSGRPLVLRRAARKRRKGSARRRSTAGGKRRRARRGGRRRAG
>NZ_CP009279.1|WP_042191483.1|5584259_5584751_+|hypothetical-protein
MAGPARIAAICGIYTAHLAVSAGIAAICGIYTAHLAVPARIATICGIYTAHLAVPAGFATICGIYTAHLAVPAGFGTICGIYTALLALLAEFATIWGIYTPLFALLAEFATIWGIYTPLFARLAEFATIWGIYTPLFARLAEFATIWGIYTPLFAQLAKLEAI
>NZ_CP009279.1|WP_042191481.1|5583023_5584118_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MKIMTILGTRPEIIRLSVIIPLLDEHAERHILVHTGQNFTASLSGIFFAELGLRAPDYVLQDKQAGLGGQLAAMFGGLESILQKEQPDRVLLLGDTNSALCAILAERMGIPVVHMEAGNRCYDLKVPEEKNRRVIDAVSTINMPYTQQSKRHLISEGFPSRRIVLTGNPIHEVMTHYESKIQASSILEQLNLISGQYFLVTAHRAENVDDPESLVQIMSGLNAVAEHFRIRLICSIHPRTRSKLTEQFSLPMNPLVEFHEPFGFFDFVFLEQHALCAITDSGTVQEECCLMKVPTVTIRRTTERPETVDCGSNVVSGVDQKSILRSVKLMAALRRDWEAPEGYLTPDVSVKVVKFLLGGNLHVQ
>NZ_CP009279.1|WP_042191479.1|5582047_5583034_-|NAD-dependent-epimerase/dehydratase-family-protein
MFNNKRIVVTGGTGSWGHELIRQLLPQNPKEIIVFSRSESAQVAMSREFEDQRLSFIIGDIRDKDALIAACRGVDYIFHLAALKHVPVCEDQPYEALKTNVVGTQNVIEAAIVNGVEKAIYISTDKAANPSNFYGMTKAIGEKLFVYANLIGSNTRFVTVRGGNVLGTNGSVVHLFMKQIKDKGQVRITDMKMTRFFFTLRDAITLLFKASEVSLGGEIFVMTMPTCRIIDLAEVLIEASGEPNVSIIETGIRPGEKIHEILMSDFESLTTVVYDEQYLVILPTLNMPELKAHYSAYPHVSFNSFSSETNLMDQEEIKSILIRGGFLQ
>NZ_CP009279.1|WP_042191477.1|5581211_5582051_-|SDR-family-oxidoreductase
MKLLILGGNGMAGHMLADYFRRQGKHHVFHTTRDKSDLGGLYVDANDIAGVEKLVDIVSPHCIINAMGVLNQFAERDKIGAYHVNGFLPHHLWRMAEAVHARLIHISTDCVFEGTRGGYTEEDVPDGTSVYAISKSLGEVRQPGHLTIRTSIIGPEIRPDGIGLMDWFLAQRGQVSGYRRVMWNGVTTLQLAKAMDTLLDSTVSGLIHLAHPKPVSKYELLQHIQAAFHKEDVEIIPEDEHVQDRTLVNTRTDVNLPLPSYPLMLQELADWMKQSEMSP
>NZ_CP009279.1|WP_042191474.1|5580231_5581215_-|NAD-dependent-epimerase/dehydratase-family-protein
MKGQKLLITGAAGFTGRHAVHLFLAGGAEVTAVVRPPSTAGALASALFPEGVKVYYCDLSNRKAVAEMIKETTPEAVLHLAGNNSVPESWRNPLLFMETNVMATLYLLEAMRSLPTSRILVAGSRLKFKPGVVAGPPHPYSLSKTIEELVSLAWGTLFKQPVLLAEPCNLIGPGPSTGFCSLLAQHIVRSEVHAGEEIPPFKLSSRYALRDFLDVRDAVRAYDFILREGTNGTIYQIDSGTQRQLGDIAEQLISRSSASIPMDWGPAQAALSIPVNGVAGDKLITSDASATPEDNVSSLGWKPGIEFSQSLTDILDYCRVNWEGRML
>NZ_CP009279.1|WP_042191472.1|5579518_5580235_-|glycosyltransferase
MRPKVSVVIPFYNCPYIEHALQSVLSQSWEPYEIIVVDDGSTVHTDLIRPYFPRIHYLGKSNGGTASALNHGILHASGDYVAWLSSDDLFYRDKINNQVLFMEQNNLFISYTNFNFINAQSQLVQMNASLLFPSHLDYLRCFLQGNPINGCTVMFKREVFGAIGLFDESLPYTHDYDLWYRAILNGYAPVMLNQSLTAYRNHEGMGTLKYYDVIMAEAAATNARYKGPLQHLISSMGG
>NZ_CP009279.1|WP_042191470.1|5578935_5579511_-|class-I-SAM-dependent-methyltransferase
MYREIKVNDFLPILLEQLKFCESILDIGSGTGTLLERYEAAVVLGLEIHRPYLLHREYKSPHIIPVHGDASHMDKLFLPKTFSAVTFIDSIEHFERKEGQRLLGMAERIAYNRVVVFTPRGFFPQEGTDHYHLQGEHYQKHRSGWEPEDFMELGYAVTVLKGFHHAQNPSFREAYGEGHAPVDALLACKTV
>NZ_CP009279.1|WP_081951201.1|5578181_5578964_-|glycosyltransferase
MPYWLAKQYKERASGEGGERMSEEPKVSVIIPFYNCPYVDLAIQSVLEQSYSNIEIIVIDDGSTLWMEKLEPFKDKIIYIRKSNGGTASALNKGIGVATGTYFAWLSADDLFHPNKINRQMQMLKITDTLFNYTAYYYVNEQGGRISETISMIFDSRTQFIETMMLGCPVNGSTVLLHMDIFRTVGKFNEKLLYTQDYDLWLRILPYYTWSYIEEPLLDYRVHNEMGSVIHKEEQKKEIEQVQARHRRVLSRLLQKERGK
>NZ_CP009279.1|WP_042191466.1|5577144_5578185_-|glycosyltransferase-family-4-protein
MKLIFPVLTLTRGGAQRMLTELANRLTEMGHEVTILLPSDGVVEYEMKCKLIYAQEGELAASDFPAGDVIISNFYTTVEVSQRASEEGKGIHVRLALCYEPTFLPDNSRSFSSYNIAPNLLVLSHWQQGIVQMNHGIKGRIVPIGVGPVFKNTKIRDRNKRLVISAIMRKPEGGFSAHREQDYLLQQLNKVKAHHPEVEIYLISPPGEQAESATLQALVNDERYQIRTPANDTELCFHYSESDIFVSSSTYDTGSLPGIEAMRCGAALVTVYAGGNKEYCTHGHNCLMSYRFENRLADDIITLIRDPSLRRRLARKGEEVSQDFTWEKSTRIFQNMLFEIVSRNPS
>NZ_CP009279.1|WP_042194464.1|5586652_5587768_-|glycosyltransferase
MPTPPLPLTPPEEEKLRGRLSGFKGGYDEGYLRGRLAILNGRSEEVFPVRNIHVMYVASGKGYPYSPLDDAVLCALQKLTAQVTITDVRQNLVELAAAQRPDLVLVLDGMDLPLEQIDALRTSGIRTAIWLTDDPYYTDFTVKIVAHYDFVFTLERNCIDFYRGLGCPEVHYLPFAAHLEHYRPTTTRSSVNREVSFIGSAYWNRVNFFREILPDLMNYNTVINGIWWDRLPEAPLYGDRIEIGKWMSPQETSVAYSGSKIVINLHRSHIDEVVNNNTLSIPAVSPNPRTFEIAATGTLQLVDARDDMGSFYKPDEEIVTFASPQEMMDKIRYYLTHEEERRAIALRAFERTLKDHTYAKRIHQMLTVIYG
>NZ_CP009279.1|WP_081951202.1|5587819_5588836_-|glycosyltransferase
MCEAVQRLNTPGVEACRPFKLMYVPQGFQAIDTGVTEALQQLVSELVISTPETMLETAAREMPGVVLVMNGLHVFPENHLEQISEIRKLGIPTAIWFVDDPYFTEDTSVICKHYDHVFTHELGCVEFYQSLGVSSVHYLPLCVNPKMFYPRRTGPQYQYDIVFIGNAFRNRTELFDELAPYLKGKKVLIAGGFWERLATYDQLTPFISNGFIPPEETANYYSGAKIVINIHRPWEEGQDNRNSYRLPSRSINPRTYEISACGTMQLTDVREDLGNYYRPGYDLDTFGSAKELQQKIEYYLKHEKERRIYALRGLRTTMRNHTFTARLPHLLNVIASRV
>NZ_CP009279.1|WP_042191487.1|5589350_5590112_+|AAA-family-ATPase
MNNTTLYLRHAELLRDQVPSFQAYPFHLPAVRTLDRLIFQKPVTFLVGENGTGKSTLLEGIAAAWGFNPEGGTLNFSFNTRSSHSSLYEYFRIARGVRRPKDGFFLRAESYYNVASYIDELDEQPGFSPPIKNSYGGKSLHEQSHGESFFAAFVHRFGGRGLYILDEPEAALSPLRQMSLLVRMHELVQQDSQFIIATHSPILMSYPEAEIFLLEGEGIRSVALEETEHYTVTKAFMNDRQGMLRELLEDEQA
>NZ_CP009279.1|WP_042191488.1|5590259_5591675_-|hypothetical-protein
MKKFWKPEYLVSLAGCGLIIYLLFVGPFIGVADNGDFLRMMNTIGLNYYDTAASYTDQFFNFSHSHFAYENLFRGFYPSSQILVVLVPRLIGGLIHGSFFDVRLLGAVYGLLLLVATWLLVKYNARGSYVTGLLLGAALLFVFYDIGYLAYFNSLFGEPVSMVFMLLTFALGLRLTSQEKPTTKGLTLFFIAILFLVTSKIQNAPIGIAFALIFLRFMTLDGERKWRKLALRFSIAIFLVSIVMYVTAPKELKHINLYQTVFFGILNESPDVKGDLQDLGLPERLEVLAGTNYFQTDTVIKQDDPSLVPDFYDRVSHKDVLFFYLKHPGRLIDNMEYAASNSMAIRPYYLGNYEKSENKPVGALSYTYSGWSEFKNKHIPHTLGFLTIFYLVYFAVAVFQYFRSRDVRGRVAGELLMLLGLIGIFSFLVPILGDGRADIGKHLFLFNVCFDMMVVVMFGWVVHKVVGIVRR
>NZ_CP009279.1|WP_042191491.1|5591683_5593576_-|LTA-synthase-family-protein
MKKQGPDRAHFFIVVILLWLKLLLLRVLFFDRIAWEWIAADVAPVLFIMGILTVITPSRVRTTVYWIFNGFLSLLLFAAAVYFNHFGSVPTYLALSEINQVFQVKASVESTIKSIDYLFFVDFVIFAIYGLIRRWKQGKTYPRERFSSRKTGFVHVVVILVSIIGGFSLSAYSVHSARGITNELVQAETAGFLNYEVVAAIKINEDNNLIGTGDIKDTIAKVDALQSSYPYSDKPAGTTPDYFGSQKGKNVIVLQLEAFQNFPLHQSLDGQELTPVMNKLADEGFYFPHVYQQIGPGNTSDAEFMSNTSIYPIGTLAMSTGFGDRELPSLPRLLRDKGYEAYTFHVNKVGFWNRNELYPALGFNGYYDKDYFTNDHFNAFGASDEQLYITGVEKLTELKKKGTPFYAQMVTASSHHPFKIPDSFKKITVPDNLKDTMLGDYLTAINYTDYAIGTLIEGLKENGLWDNTVLVMYGDHFGLQPQDVPPEQVESALGVPYDSRISRFNIPLIVRVPGMEQGKVVERTGGQLDILPTIANLMGVSLQQEGYTAFGHDLLNIDRNVLGMRYYLPSGSFFNDDILYVPGKGFADGEAVSLDTLKPVTDFSKYQSDYEYVLKLMNLSDEYVKLLPQR
>NZ_CP009279.1|WP_042191493.1|5593772_5595110_-|5'-deoxyadenosine-deaminase
MGNILIKDAEIITMNKQEEIIVGDVRIKDDIIVEIGIGLIPQGDEKVIDATNRTLIPGFVQTHIHLCQTLFRGKGDDLELMDWLRKRIWPLEAAHDEESLYYSAMLGIGELISSGTTTIVDMETVHHTDYAFQAIAKSGIRALSGKVMMDQKGGDVPEALQEDTASSLQESVDLLEKWNGYGNGRIQYAFSPRFVISCTEPLLTEVRDLSARYDVKVHTHASENLGEIEIVQAMTGMRNIVYLDHLGLANERLILAHCVWLDVEERRILRDRGVHVSHCPGSNLKLASGIADTPGMLHDHVSLSLGADGAPCNNNLDMFNEMRLAAIIQKPQYGPTTMDARSVFRMATIGGAKAVGMEDKIGSIEVGKKADLVLLNLFNFHTFPSYDVDPISRIVYSATRADVETTIIDGEIVMERGLLKTVDKEIVLNEANRSIKRLLKHTSIV
>NZ_CP009279.1|WP_042191495.1|5595534_5596014_+|hypothetical-protein
MPTISQTPNELQAFIAAAEKVWFEVYDSADSRRVIRVDGADYYRLPVRFSTRAKVISYFRKYWGITMSNTMICNLKTVSRNNRLYVISGDTGTIAFIPRRLTVTGRTSTRIRLTAVLSIDDMSDEDIVNVRYLIGVSGRRLLILNRDQKNTDTRYQTCR
>NZ_CP009279.1|WP_042191497.1|5596075_5596603_-|GNAT-family-N-acetyltransferase
MQVGNGIRKARQDEIEEIMELISKCVQVMQAAGSDQWDESYPNKEIIELDIAQGTLYVCEEDQAIAGILVLDENASEEYKKIEWKQNQGPHLIMHRLAVHPHIQGKGIATRLIAFAEDYAARNGYTSIRLDTYAKNTRALEIYPRLGYDHRGEVGFPNRTANFPVFEKVLKPEHS
>NZ_CP009279.1|WP_042191499.1|5596809_5597226_-|hypothetical-protein
MKKKSLRTLRSGRTRRRTLLLSRKTKVRRGLARKPRRGLARKVVRYGKTKKGLLVRKKRRLRRKLVRKVRVIQAPVHVVPVIEAPPAPQVIPLPPDLGVSPETPPADAFQQGYTEAYNVGFDAGFAKGFEDGHKLEFN
>NZ_CP009279.1|WP_081383034.1|5597230_5597491_-|hypothetical-protein
MIRSISRSQAALAAILESIAELTGQSELTARKLSDNIRILSGYQSAMCRMMSGISLHQPKRGIPAAPWLSKAYAVGTSRDHGAQEE

Crispr_ID: NZ_CP009279_6

• CRISPR_ID: NZ_CP009279_6
• CRISPR_location: 5626991-5627080
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_6

Consensus_repeat	Method
CTTGAGTTACTCCGCAAAACTTGCTTCGT	CRISPRCasFinder

spacers of NZ_CP009279_6

>6.1|5627020|32|NZ_CP009279|CRISPRCasFinder
AAGCATTCACATAGTTTTGTTAGCATAATCTG

CRISPR arrays and Neighbor proteins around NZ_CP009279_6

CRISPR arrays

The CRISPR arrays of NZ_CP009279_6

>merge|NZ_CP009279|6|5626991-5627080|CRISPRCasFinder
CTTGAGTTACTCCGCAAAACTTGCTTCGTAAGCATTCACATAGTTTTGTTAGCATAATCTGCTTGAGTTACTCCGCAAAACTTGCATCGT

>NZ_CP009279|6|6|5626991-5627080|CRISPRCasFinder
CTTGAGTTACTCCGCAAAACTTGCTTCGT	AAGCATTCACATAGTTTTGTTAGCATAATCTG
CTTGAGTTACTCCGCAAAACTTGCATCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042191526.1|5629570_5630872_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|181512
NZ_CP009279.1|WP_042191531.1|5632503_5633250_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP009279.1|WP_042191524.1|5628774_5629392_+|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl|CDD|378988
NZ_CP009279.1|WP_042130872.1|5635651_5636107_-|chemotaxis-protein-CheX	unknown	unknown	gnl|CDD|381734
NZ_CP009279.1|WP_081951204.1|5623661_5624705_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|238558
NZ_CP009279.1|WP_042191541.1|5637332_5638142_+|histidinol-phosphatase	unknown	unknown	gnl|CDD|213994
NZ_CP009279.1|WP_042191534.1|5633246_5634749_-|DEAD/DEAH-box-helicase	unknown	unknown	gnl|CDD|223587
NZ_CP009279.1|WP_042191539.1|5636360_5637263_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP009279.1|WP_081951203.1|5616135_5623086_-|hypothetical-protein	unknown	unknown	gnl|CDD|366376
NZ_CP009279.1|WP_042191529.1|5631281_5632502_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|377581
NZ_CP009279.1|WP_042191518.1|5624877_5625621_-|2,3-diphosphoglycerate-dependent-phosphoglycerate-mutase	unknown	unknown	gnl|CDD|184516
NZ_CP009279.1|WP_042191520.1|5626168_5626954_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_CP009279.1|WP_052404407.1|5608420_5613850_-|WIAG-tail-domain	unknown	unknown	gnl|CDD|333735
NZ_CP009279.1|WP_042191516.1|5615270_5616062_+|phosphatidylserine-decarboxylase	unknown	unknown	gnl|CDD|179544
NZ_CP009279.1|WP_042191513.1|5614089_5615184_+|YheC/YheD-family-protein	unknown	unknown	gnl|CDD|373047
NZ_CP009279.1|WP_042191537.1|5634846_5635623_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|223377
NZ_CP009279.1|WP_042191511.1|5607370_5608219_-|glycosyltransferase	unknown	unknown	gnl|CDD|275103
NZ_CP009279.1|WP_042191509.1|5605656_5606394_-|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133029
NZ_CP009279.1|WP_156113183.1|5606390_5607374_-|glycosyltransferase	unknown	unknown	gnl|CDD|275103
NZ_CP009279.1|WP_042191522.1|5627125_5628631_-|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042191526.1|5629570_5630872_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|181512	PRK08637, PRK08637, hypothetical protein; Provisional.	0
NZ_CP009279.1|WP_042191531.1|5632503_5633250_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	3.63162e-81
NZ_CP009279.1|WP_042191524.1|5628774_5629392_+|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl|CDD|378988	pfam12900, Pyridox_ox_2, Pyridoxamine 5'-phosphate oxidase. Pyridoxamine 5'-phosphate oxidase is a FMN flavoprotein that catalyzes the oxidation of pyridoxamine-5-P (PMP) and pyridoxine-5-P (PNP) to pyridoxal-5-P (PLP). This entry contains several pyridoxamine 5'-phosphate oxidases, and related proteins.	1.09055e-28
NZ_CP009279.1|WP_042130872.1|5635651_5636107_-|chemotaxis-protein-CheX	gnl|CDD|381734	cd17906, CheX, chemotaxis phosphatase CheX. This family contains CheX CheY-P phosphatase which is very closely related to CheC chemotaxis phosphatase; both dephosphorylate CheY, although CheC requires binding of CheD to achieve the level of activity of CheX. CheX has been shown to be the most powerful CheY-P phosphatase of the CheC-FliY-CheX (CXY) family. Structural and functional data of CheX and its CheY3 substrate in Borrelia burgdorferi (the causative agent of Lyme disease) bound to the phosphoryl analog BeF3(-) and Mg2+ reveal a unique mode of binding, but a catalytic mechanism which is virtually identical to that used by the structurally unrelated CheZ, providing a striking example of convergent evolution. Thus, CheX is quite divergent from the rest of the CXY family; it forms a dimer and some may function outside chemotaxis. The data also suggest a possible CheX regulatory mechanism through dissociation of the CheX homodimer.	6.65052e-39
NZ_CP009279.1|WP_081951204.1|5623661_5624705_-|ABC-transporter-substrate-binding-protein	gnl|CDD|238558	cd01138, FeuA, Periplasmic binding protein FeuA. These proteins have predicted to function as initial receptors in ABC transport of metal ions in some eubacterial species. They belong to the TroA superfamily of periplasmic metal binding proteins that share a distinct fold and ligand binding mechanism. A typical TroA protein is comprised of two globular subdomains connected by a single helix and can bind their ligands in the cleft between these domains.	5.58335e-63
NZ_CP009279.1|WP_042191541.1|5637332_5638142_+|histidinol-phosphatase	gnl|CDD|213994	cd12110, PHP_HisPPase_Hisj_like, Polymerase and Histidinol Phosphatase domain of Histidinol phosphate phosphatase of Hisj like. Bacillus subtilis YtvP HisJ has strong histidinol phosphate phosphatase (HisPPase) activity. The PHP (also called histidinol phosphatase-2/HIS2) domain is associated with several types of DNA polymerases, such as PolIIIA and family X DNA polymerases, stand alone histidinol phosphate phosphatases (HisPPases), and a number of uncharacterized protein families. HisPPase catalyzes the eighth step of histidine biosynthesis, in which L-histidinol phosphate undergoes dephosphorylation to produce histidinol. The PHP domain has four conserved sequence motifs and contains an invariant histidine that is involved in metal ion coordination. The PHP domain of HisPPase is structurally homologous to other members of the PHP family that have a distorted (beta/alpha)7 barrel fold with a trinuclear metal site on the C-terminal side of the barrel.	5.58778e-82
NZ_CP009279.1|WP_042191534.1|5633246_5634749_-|DEAD/DEAH-box-helicase	gnl|CDD|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	6.67667e-122
NZ_CP009279.1|WP_042191539.1|5636360_5637263_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	2.27256e-57
NZ_CP009279.1|WP_081951203.1|5616135_5623086_-|hypothetical-protein	gnl|CDD|366376	pfam00933, Glyco_hydro_3, Glycosyl hydrolase family 3 N terminal domain.	3.61768e-66
NZ_CP009279.1|WP_042191529.1|5631281_5632502_-|ABC-transporter-permease	gnl|CDD|377581	pfam05975, EcsB, Bacterial ABC transporter protein EcsB. This family consists of several bacterial ABC transporter proteins which are homologous to the EcsB protein of Bacillus subtilis. EcsB is thought to encode a hydrophobic protein with six membrane-spanning helices in a pattern found in other hydrophobic components of ABC transporters.	6.29749e-74
NZ_CP009279.1|WP_042191518.1|5624877_5625621_-|2,3-diphosphoglycerate-dependent-phosphoglycerate-mutase	gnl|CDD|184516	PRK14115, gpmA, 2,3-diphosphoglycerate-dependent phosphoglycerate mutase.	1.09711e-149
NZ_CP009279.1|WP_042191520.1|5626168_5626954_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	2.71689e-26
NZ_CP009279.1|WP_052404407.1|5608420_5613850_-|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.	1.91243e-41
NZ_CP009279.1|WP_042191516.1|5615270_5616062_+|phosphatidylserine-decarboxylase	gnl|CDD|179544	PRK03140, PRK03140, phosphatidylserine decarboxylase; Provisional.	2.44975e-96
NZ_CP009279.1|WP_042191513.1|5614089_5615184_+|YheC/YheD-family-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.	9.39785e-79
NZ_CP009279.1|WP_042191537.1|5634846_5635623_-|SDR-family-oxidoreductase	gnl|CDD|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	7.59945e-84
NZ_CP009279.1|WP_042191511.1|5607370_5608219_-|glycosyltransferase	gnl|CDD|275103	TIGR04283, glycosyl_transferase_family_2, transferase 2, rSAM/selenodomain-associated. This enzyme may transfer a nucleotide, or it sugar moiety, as part of a biosynthetic pathway. Other proposed members of the pathway include another transferase (TIGR04282), a phosphoesterase, and a radical SAM enzyme (TIGR04167) whose C-terminal domain (pfam12345) frequently contains a selenocysteine. [Unknown function, Enzymes of unknown specificity].	1.37238e-16
NZ_CP009279.1|WP_042191509.1|5605656_5606394_-|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.	2.2412e-50
NZ_CP009279.1|WP_156113183.1|5606390_5607374_-|glycosyltransferase	gnl|CDD|275103	TIGR04283, glycosyl_transferase_family_2, transferase 2, rSAM/selenodomain-associated. This enzyme may transfer a nucleotide, or it sugar moiety, as part of a biosynthetic pathway. Other proposed members of the pathway include another transferase (TIGR04282), a phosphoesterase, and a radical SAM enzyme (TIGR04167) whose C-terminal domain (pfam12345) frequently contains a selenocysteine. [Unknown function, Enzymes of unknown specificity].	2.06758e-13
NZ_CP009279.1|WP_042191522.1|5627125_5628631_-|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].	1.15129e-105

Protein sequences

>NZ_CP009279.1|WP_042191520.1|5626168_5626954_-|helix-turn-helix-transcriptional-regulator
MLHASPSSFVILPALAKIVCEPSWKWQKREKSLQNYDLFYVWSGEGTVIRNGEPFQVGKGSCFLFRPGDHTSATHNPQRPLVLTYIHFDVTGEVTDVPLPYRVLAETVEFEHLLARYVRLFLVDTYAAEEEGQLVLKQLMIHLLREDRVKPVERYASNHLTEIIHEIANYVSQHPGISHRVEDLAARAGLSPRYFSIKFKELTGSSVQSYVIRARIERAQHLLLYAGMNVTEVADALGYRDIFFFSRQFKQYTGKSPSEIR
>NZ_CP009279.1|WP_042191518.1|5624877_5625621_-|2,3-diphosphoglycerate-dependent-phosphoglycerate-mutase
MYEIVLIRHGESQYNVQNLFTGWSDPDLTEKGIQEAKAAGKLLKDEGYTFDLAFASVLKRSIKTLNYVLDEMDLLWIPVQKSWKLNERHYGALQGLSKSETAIKYGEEQLHLWRRSLSVRPPLLELNDPRYARNDIRYSSIRPEDIPRGESLEDTVHRVGDFWRNRIVPLVRKKERVLISAHGNTLRALIKFMEDIDEAALLELNIPTGVPLVYKLDEDINPISRFYLGDPEQVAAKARDVAKQGHV
>NZ_CP009279.1|WP_081951204.1|5623661_5624705_-|ABC-transporter-substrate-binding-protein
MIISIIIYYVDWSEFILFRSPKTYLLLVFTLVISLLLAACGQAVEHTTSSVDGTESAVSLSNSNDSSSEVDMITYQASNGDIQVPRHPKRIVDLTSFDTGYFLALGIKPVGVMNGVLNSPYFEGMLEGVQGLGAEPSLEHILELNPDLIVVFSGMEGLDKLAEIAPVVAIQYGAKTIRDQMLDFGTLTGKEAEAKAWVEQWNKKIKELKPQVLAAVGDKTVSILNPFSGGLFVFGHSYGRGGEIIYNEFGLKAPPEAQKEAIDSGTGWATISLEKLPQFAGDIVFTCPWAGDTSDPKIVYDNPLWEHLPAVKTGNVFQLDPTADTYSDPVTLEAQLNYITESLLSAK
>NZ_CP009279.1|WP_081951203.1|5616135_5623086_-|hypothetical-protein
MRKNCNRLLKILFCCILITSIITPSTSSPVLAKVLPGLADVSREVAAEGIVLLQNPEYKPAGSQVNENEQVLPIKMSENVSVFGRIQAHYYKSGTGSGGAVRVDYVNGILEGLRNNPSLKLNEDLAKVYADWIKKNPFNNGGGGWAAEPWSQAEMPLTDEIVDAAKAKTDTAVIIIGRTAGEDKDNTDVKGAYKLTDLEVDMLNRVYAKFDRVAIVLNVANVIDMSWAKNYPKAAILYTWQGGMEGGSAVADVLTGDVTPSGKLSDTIAATLADYPSTAHFGSKTENSYSEDIYVGYRYFETLAPDKVLYPFGYGLSYTNFKITTDNVNAGENEVAVTVTVQNTGKVEGKEVVQIYYGAPQGKLGKPAKELAAFAKTRLLQPGESQSITITYDTKDMASYDDSGITGHDSSYVLEAGDYNIYVGNSVTDSEKQGVYSLNALKVVETLQEALAPTKEFDRIKPGQPNENGTFTTVTEKVPTRTTDLDERIKQNLPASIPQTGDKGYTLLDVYNQKVTMDQFIAQLSNNDLGAIILGEGMSSPKVTAGTAAAFGGVTKNLLKFGLPIDSAADGPSGIRMETNAEKATSIPNGTMLACTWNTELNERLFNLLGKEMLINNIDTLLGPGINIHRSPLNGRNFEYFSEDPLLTGIMAAAQTRGLQKNGTSPTIKHFAANNQETDRHLVNALVSERALREIYLKGYEMAVKSGKARSVMTSYGPVNGTWASSNYDLNTTILRGEWGFDGIVMTDWWAKMSEDQGFYATTNRYDETNGKAMVRAQNDLYMVIPNDYAETHKNRNNSTFNTMTSLANGSLTLGELQRSAKNITSFLMKSPAFARTAKIDYVVNYTPGRDWFRVNTDKSGDPQLSDITVGGKKIKIFNPLKLDYKAFGETTETSSYPEVKATAIAGVDVSIRQADKDRPAAVITASAGGEKRIYKVIFSSEEGLEPIFENPTYAYLKNISIDGKPLEGFAQTRFSYDVGLSNGATLPEVTFETNDGVKATANVDLINKRVTIKCISSDQANSYVIQFGTTPQSDEFDSTNLSNFWTINKETATNTENNKNWSLSTALGNLRIIAERGDFWSDHADLKNYFQQEAFGNWEATVKINMSKAPNQNYNGVGITASQDNNNYIWVKYEYSSGKIIGMTKETGGTEPVTIGQLSASQLTSIFGEKKELYLRLKKIGNSYSGYVSADGKEYISLGSTTANYANPKFGLLASNGSQNLTDPFVVDFDYVRINSDVALAVKKIGKNTKLKVAETEFASITPIITPVSSNDVDGGLCYTNTSKGEAISYKVNVEKEGMYKVTSRIRSSQSDVAQMSFGIYDGDKLLGTFDLTTTKGVWKTFRIPDIQLSAGEHTLRIVFESAGIDLNWLTFQLKQDNVDTSALEADIKAAQNIDMNAYTAYKKLKFNTVLDEVKAVLAEPINDEVVAEAIASLKAAITDLSISSMPINIAPRETLKVENGIRIYPYNAPWIYATNTQFRFESGTDAMSYVNSNDLVYFGQVDLTNLVEVRVQYAREGGSSPSFKFYTEADNTGKPVKRATTQGRAYADAYSGGGSFELGNEFASISFAQKAGAAWGNYGMASTKQTPGNSYIDHYLTAETFLDRTKVTGKQNVYMIFNGLNANLQYVELIYADPIEVTFDQNYLDSPAPTKVTAFKGEAISTLPRVPEREGYIFAGWFDNKEGTGDALTVDTVMNISTVYYAKWTEDTHAKEIISIVKPQLLSVPFGTAAGELNLPATVEATLGNKRVIHLPVQWDSKDFNGGKAGSYTLAGSFELPEGVLNSTHQTVSITVVVLPEGTKPIQITKVEKLEGKNVEFGTAFDKLELPSSATVTLDTYEQKELVVKWSPAGYNGNVEGSYVLSGTMVLEEGMINPNDLKASITIQVMPEVIRVAEIVTVQDLESKSVPFGTPFNGLKLPSSVIATLNNGETKAISIDWNSEGYNSDKQGAYILKGALVPLEGVSNPKDLKASITIEVLPEVITIPEITAVQALASKSVAYGTSFDALELPASVSVTLNTGMNKVVSVQWNKEGYNGNTEGTYTIKGDLVFPEGIANPLGLKVQISVIVKPYSGGAGGQPSTPTPTTPAVPSVPSIPGEVVKPGEQQPPKTDGKTKTPELIRQELKNKFKDATLIPSWAESAIAALVERNIIGGRTDGSFDPSGKVNRAEFVAMVVKSFNFSMGENQKQFTDVLKDAWYQNYVEIGTSNQLINGIGNGMFAPNSSISRQDLCLILFNALKKLNVELPQATNHDFPDDASIAGYAKEAVYVFKDLGIVNGGSGGEMDPTASASRAEAAVIINNVLDYYASVTSSKVK
>NZ_CP009279.1|WP_042191516.1|5615270_5616062_+|phosphatidylserine-decarboxylase
MVKQLLRLMTELSSHRWLSRLMGSFSHSRLSRFLIPVFIKTYQIPSAQAEKNPGEYLTLNEFFSRRLKPGMRPIATDADALVSPVDAMITAMGDISSGTIMNVKGQDYKIEDLLNHSPHLELYKRGFFFVLYLSPTDYHRIHSPLTGHKVESDHIRGRAYPVNDFGMRHMKGVLNRNERLITYIAGDYGETAVVKVGAMNVSSIGYTDANATEWQIGDDLAYFEFGSTVVLLMESGTFTPRPKLEVNTKVKMGELLGTLHRPL
>NZ_CP009279.1|WP_042191513.1|5614089_5615184_+|YheC/YheD-family-protein
MGHKLVGILLNADMHRGVPRLKTGQESLSNYEEAAAAYGLVPCFLKLADIDTDSGFSAAYIKGSHGYKSVVVPTPTVIHNRAIYSQNSPGMQRLLRHHPLVYNTCNRYGKDEIHELLEQHEELREVLPATTGVSGLKQMMNRYPDLILKPCRGSIGNGVMRLVRKGPQRWSLNYLSPSMRRWISTPVYQGALPKMLRARLASVPYLVQERIPLAEIGGRPFDLRVTIQRGWGGDWQVTGLFAKLAPPGGFVSNIARGGEALSSSFALEKAFSRGIAAHIRIAVETLSLVIARCLEQDLPGLADIGLDIGITKDGRIFFIECNGRDQRYGFHKAGLTEIWKESYRRPMGYARFLLEKNSLIYNSY
>NZ_CP009279.1|WP_052404407.1|5608420_5613850_-|WIAG-tail-domain
MRGSKKKQPRSPQKRLYYVDNPNIKELSMLESKGSSKDSGSSNDGVSKAELADVQVSGGAIAEVVQEESIFVPVLQPEPEPEPEPEPEPIVEEQLQKQADNLPETIWFAPEKERFQPVYTDDLSDAAVTGAKIAPRTIDGSKLKFGIIGTPWLQDYAVQSINIADKAVTSSKIAPESIVGEHLAEGSVSGGKLLDHSISGEKLKNGSISPEKLADRIIGGGQIADKSIESRHLSDLIITADLLEDGAVTGEKIGSSSITGRHIANGSIDRSKLADAAVSGDIIADGEISSSKLADAVIEGRHLSDALITARHLAPGAIGPGQLASKLIGKEQLQSGVIEGAHVADGAIGSKQLGAEVVRSIHLSAESVHGSHISDGEITSRHLADRSISFLKLTEGAVGTAQLVEQAVTSSKIADQSILAHKLADEAVTTRHIAKSAIRGPQIAMQAVSSNHLEREAVNHSHLASEAVGSEQLMDEAVHTEHLSSGAVTGEKLASESVGAEHLRPQSVTSAKLADGVVSSAKLAAGSVIGSTIAREVVSGEHIAFCAVEEKHLADASVSGRALQDAVVDKDHLATGAVERRHLGENSVTTAAIQSGSVSGDKLASAAVREIHLAAGAVQPHHLADHVVTSLKLSPESVSTDKISDLSVTSAKLADGSVDSSKLAVSAVQAEHLSVNAVHSKSISDSAVQSRHMNPGSIGGAHIRPLSIGNGHIIPNSISSIQIQEGSISGSKLAKGAVDSQHLSPGSVDGSHLCMDTIEGRHIGHGEIKLAHLAEDARSSDLLPEGSITGEKLAEESVDSIHLVPASVDGTHLRLGAVEGRHIQHGEITLAHLAEETFSSELLPNGSITGEKLAEESVGSIHLMAGSVDGSHLSSDTVKGRHIGHSEITLAHLAKDARSADLLPDGSITREKLAEESVNSNHLIPGSVNGSHLSPDTVEGRHIGYGEITLAHLAKDARSADLLPDGSITREKLARESVNSNHLIPGSVDGSHLSPDAVEGRHIRNGEITLAHLAKETRSSELLPDGSITSEKLAVESVDSNHLVPGSVDGSHLSPYAVEGRHIRNGEITLAHLAKETRSSELLPDGSITSEKLAEESVSSIHLEPGSVGSSHLSSGAVEGHHIGYGEITMAHLAPETRSSELLPDGSITGEKLAEESVSSIHLEPGSVGSSHLSWGAVEGHHIGYGEITMAHLAPETRSSELLPDGSITGEKLAEESVDSNHLAPGSVDGSHLSSGAVERRHIGYGEITLAHLAPETRSSDFLPDGSITGEKLAEESVDSNHLAPGSVDGSHLSSGAVERRHIGYGEITLAHLASETRSSELLPDGSITGEKLAEESVDSNHLAPGSVDGSHLSLGAVEGRHIRYGEITLAHLASETRSSEFLPDGSITGEKLAEESVDSNHLAPGSVDGSHLSLGAVEGRHIRYGEITLAHLASETRSSDFLADGSIPGKKLEGGSISAFHLAPGSVYGGHLAGGTIDSRHIRQGSINLNHLAEEVFSADLLPDGSITGEKLEGGSIQSFHLAPGSVYGGHLAGDTVDSRHIRSNSITLKHLAEEVRSSELLPEGSITEEKLAEGSVNASHLQPWSVYGEHLADQIVADRHLQPGIIKLEHLADETRSSALLPDASIDGVKLKAGSIESSHLADGSVGTTELQDESVVASKISSFAIQARHLEEESVQDYHIAPGAVNGAHLAVNSVNAEHLSFSPIQTAGKREALQQFGMTAFMFNGDAESVEVTVSFDENFGHTGYVLVAMTNQPYFYASLKSRANGDAVIQVVRLRETPHFYGVISWIAIGAPLAKPVVDDRVFD
>NZ_CP009279.1|WP_042191511.1|5607370_5608219_-|glycosyltransferase
MSMKPKRTSARRTGRRVSRIKRRTSRPVRQVAAIPIVNHPNPYVSVIIPAMNEAKTIAGVISGARRVHPRCEVIVIVNGSADQTAEIALSLGAHVISYELPLGHDAGRSVGAEVAKGEVLLFTDGDLVIPASGLRPFVTAISGGADIALNDYSGPVRRLSPHPVVLSKHALNILLGRPDLKGCSMTAVPHAISRRALEILGSQSLSRPPLAHAQAVLSGLRVVAAHKVHVGKLNAVRRKEDGTDPLQQLITADHMEAVSLLLEHRGIRAGFSDGTRRREMVR
>NZ_CP009279.1|WP_156113183.1|5606390_5607374_-|glycosyltransferase
MMVALLQVSGSSAVRRGTATRTVKKRSASSQAKTTLAPRQRVANRSVKRGIPTARPPILSRQSKVGRELLNLPSLRGTLSVIISARNEEQTLGRLLQQVSLLGPTEIIVVLNGCSDSSFPISRQHRQAIVVHCPESVGHDVGRAIGAKLSRGDILLFLDGDMVIPASQLGLFTAAVDGGIDVALNDLDPLMPSFGLCDDVTRSKLFLNYALGRYDLGVSSMTAVPHALSRRALETIGYRELIVPPKAQARSVLEKLRVEKVGTVNVIKHNRLRQANIGAGNAVEKLIIGDHAEALLEVLSRRDDGGLLNSETQREYRRQVAAWRNRI
>NZ_CP009279.1|WP_042191509.1|5605656_5606394_-|glycosyltransferase-family-2-protein
MTMTSIIIPTYNALPLLRSCVESIRAYTPLPYEIIVVDNASSDGTDAYCRANRITFISLPENRGFPSACNLGLLLASGDELLLLNNDVVVSHRWLTNLKRSLYSAPEVGIVGPVTNYASGRQQVKTDYESLLDFHKAAEITNRSNPQKWLETKRLVGLCFLFKRELLTSVGLLDERYSPGHYEDDDYCYRARLKGYRLLIAGDCLVHHEGSASFKQVYHTGLQELVERNRKLFMNKWNVDPTSFI
>NZ_CP009279.1|WP_042191522.1|5627125_5628631_-|PLP-dependent-aminotransferase-family-protein
MNITLAFDQYLAIHRYKYLALYHALRAGILEGTLPGGTQLPSTRSLAMHYDLSRGSVSQVYEMLLADGYVRTVTGRGTFVSKDSFVSASGDNKRENVTSGEVADAAGGGSASERTIPLSAWGERLLTRPTPLYEQRSKNVVSFLSGGMRMEHFPYAEWRSALTYAGGKEGGMLQSTCPPEGDEGLRKAIAAHLRITRGIRADVEHIVLFSGSMQGIVILTQLLLDAGGEAVVEDPGFHGIRRAVEINGGRLLVGKLDDSGLIPEDWDARLLFVTPSRQFPTGVVLPLERRRILLEWAQRHEAVIIEDDYDSEFRWSGRPIEPLKALDRGERVVYIGSFSNTMFSGLRLGFAVLPPSLVKSTIAAKALYEPLPVGLLEQRALARFMNTGGYGRHLRRMTRIYGERGRILRAMLSEQFNELFELLPGDAGLQVYGRWLRSREEFVAFRAAAHRRGTDFRDVALYQVSPGEPAACFAFAHLNAVELEEGIKRLLLAWEDVQTAT
>NZ_CP009279.1|WP_042191524.1|5628774_5629392_+|pyridoxamine-5'-phosphate-oxidase-family-protein
MRRKEFQVDQEEELISFLDGMSFGFLGTSDEQGLPRVTPLNFVYTDGCFYFHGSHAGGKMKAIRNQQKVCFTVADEYALIPSYFSDPEMACPATAYFKSVTAYGIAEPVEDISEKAIVLSLFMKKLQPEGGYNQIDAEDPKYRPRLKGVAVVRITPDEITAKFKFGQNLKEEGRSGVISGLSERNHPRDEETIEMMKKYCPYHSE
>NZ_CP009279.1|WP_042191526.1|5629570_5630872_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MNPLAGQLNESIKAGNEHVYDMLSTLGKEIYFPKEGILSQSAEAGAHAKKYNATIGIATEGGVPMHLGVIQDKLSAYSPKDLYSYAPPAGKPELRTVWREKMLRENPSLEGKTISNPVVTNALTHGLSIVADLFAEPGDAIIYPDKNWENYELTFGIRRHGETVNYPLFTEEMTFNSTGLEEALLAQKERGKAIVLLNFPNNPTGYTPGIKEGDEIVAAILRAAEEGINVVVVSDDAYFGLFFEDSLKESLFGKLAHLHPRVLPIKIDGATKEEFVWGFRVGFITYASEDKDLLAALEQKTLGIIRATISSGAHPSQTFVLDALKSPQFEEQKEEKFQIMKGRANKVKTLLDSGKYGDDVWTYYPFNSGYFMCLKLHTVSAEALRLHLIHNYGLGTIALGETDLRIAFSCIEEEQLEDLFDLVYAGVRDLEKA
>NZ_CP009279.1|WP_042191529.1|5631281_5632502_-|ABC-transporter-permease
MDLKELRRTRRGRFMGSMLPYVGYIIQSGVAMVFLFVLIVFSAWYTSLLQNVPEGIPIRWIMLAILLPAAVNSSFRTYLQTPDTIFLLPQGHRMKEYFAPSWVSGNVWKIVRLLFVLITLWPLYIRTDDSPKRLLFTILILIAVKLVASYGLWKEIAMLSRPMAGIFTFLRWAVGGLIIAAWLWQPAGRSLIFMALLAAAYLVALSVPGRHAVPWERLIAMEKNQGGRALMVLGWFVDVPGREQRVYPRRYLSKWGARLPWRKDTAYRYLLTKSFARGDIFGIIMRISVLALLLNWLNHDSYFGTAIYLFFLFIIGVQLSALRKLHSESFWLTVYPFPEGSKADNTTQFVFRAHLVVALILGLPFLASIGDRLLPVIGTFVAGVLVSFLFKGYLSRKAAKMADEDL
>NZ_CP009279.1|WP_042191531.1|5632503_5633250_-|ABC-transporter-ATP-binding-protein
MNNSPVLQITGLSGGYSLNKPVLHDIALQVQPGEMVGLIGLNGAGKSTTMKHILGLMSPHKGDITVKGKTRAEDPIGYHNALSFVPESPLLYDEMTVREHVEFTARAYGVEQSDYETRTLHLAKLFHMEDKMDTLSTHLSKGMKQKVMIMCAFVARPALYVIDEPFLGLDPLGIRSLLDFMMDLKKSGSSILLSSHILSTIENYCDRFIVLHRGKVIAQGTLAEIAASTGLQGLTLEQLFYELVQGGK
>NZ_CP009279.1|WP_042191534.1|5633246_5634749_-|DEAD/DEAH-box-helicase
MNKASFAAIGIQEDLVARLSEFGINAPSPVQEQTIPLLLEGRDVIAASQTGTGKTLAYLLPLLQTINPEQKVVQKLVLAPTQELAMQILREAERYGEHRGIRVMGLIGGAAIKRQIDKLREHPQLVVGTPGRIRELIGLRKLKMHEVSTIVLDEADQMFQLSGAGEVTKIVSSALRSRQLVMLSATIGPETKALANREMKNPAEVGIAPGVMTAESLEHHYVVTEERNKIDMLRRVIRHYNPEKAIVFVNATDDIAEVEAKLNHLGLTAAALYGDADKVTRSNVLSRFREGKFRVLVASDVAARGLDIENLSLVVSFDPAFDSEHYVHRAGRTGRMGKRGLSVTIVTEQQTFIMRKFARELDIALEEREMVGGKVLAADEARNALNSGRGRNESSGQRRDASSPRSSKPQARTSGNAGTQPSTTSTEQQPVKRLATIQTSEASVESQRDSQRSVNPSAGARGGATPARSKRSSNAEREKNRKNKGAPKWLKDKTPRGDGQ
>NZ_CP009279.1|WP_042191537.1|5634846_5635623_-|SDR-family-oxidoreductase
MVLKDKVVVITGASSGIGALTAQMLSKQGAIPILVARSEAKLKETAAGIPGVFGLYTCDVTDADGVQETFAQILATYGRIDILLNNAGYGKFAAFTEMEPHEFDDMMDVNYMGIVRCTKAVVPHMLERGSGQIVNVASMAGKIGTAKSVAYTATKHAVLGFTNALRQELRKSGIIVSAVNPGPIATDFFKTADPSGNYEKSVARMMMTPEHVSSKIVKVMETGKEEIDLPGLAGFGIRLYGLFPRLADKLTYNAMNRK
>NZ_CP009279.1|WP_042130872.1|5635651_5636107_-|chemotaxis-protein-CheX
MKAEVINPFLESARTVIEQVIQVSPSTGNLGIKEIELIDNHIWIQVGMTGQLSGNIIFGIAEQVALRMVSIMMGGYVITEMDEMGQSAISELGNMISGNASTILYNQGVSVDISPPQIMKLESMSFLPRRALSIPLLMDGVGEMDIQVMIS
>NZ_CP009279.1|WP_042191539.1|5636360_5637263_+|LysR-family-transcriptional-regulator
MNISQLETLITISKTMSFRKAGELLNLTQPAVSAQIKSLEEEFKTQLVDRNQPVTLTDRGTVFLEHAEQIVTIVEELKQRLADLEDNPQGHIILGTTTSIAIQILPRILSYFKDQFPHIKTSISSMSSSQIYQHVENGIVDVGIGYLIGRSPSMTTSILYYDTFELVVSPRHPLAQVKTAGIEALNKTPLILLSPDTVGRKFADEVFSKHGIEPQVIMELTSSEEVKRMVELDLGAAIISKQSVTAEVRAGSLKIVPIIELEVTHPVGVITKSGKYVNSAMRQFLSDLKGMPETQFIGSE
>NZ_CP009279.1|WP_042191541.1|5637332_5638142_+|histidinol-phosphatase
MKFDLHTHHFRCGHADGTIRDYIEAGISAGLGVIGISDHTPYFGSPSEQAFPLIAMGKSEFSNYVEEVLSLKKEYEGVIDVLLGIESDYFPEHAELYRKTLSAYPFDYVIGSVHSVGGVSIFNKGRWKGLSKNEQIRVKSDYYRLIADSARSGMFQILGHIDAMKGNYPAFSEIPAPKPIDDCLQVISECGVAIEINTSGGTKLVGGWYPSEDILERAHHFGVEVTFGSDAHKPSRVAEDRDAVAAQLKAIGFTHWVYYKQREKIKVSL

Crispr_ID: NZ_CP009279_7

• CRISPR_ID: NZ_CP009279_7
• CRISPR_location: 5657172-5657271
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_7

Consensus_repeat	Method
GTTATTTCAAGCGGAGCCTATGCTTCGTAAAAC	CRISPRCasFinder

spacers of NZ_CP009279_7

>7.1|5657205|34|NZ_CP009279|CRISPRCasFinder
AAAGCGTATGCTTCCGATGTTAGTTTTACGCGAT

CRISPR arrays and Neighbor proteins around NZ_CP009279_7

CRISPR arrays

The CRISPR arrays of NZ_CP009279_7

>merge|NZ_CP009279|7|5657172-5657271|CRISPRCasFinder
GTTATTTCAAGCGGAGCCTATGCTTCGTAAAACAAAGCGTATGCTTCCGATGTTAGTTTTACGCGATGTTATTTCAAGCGGAGCCTATGCTTCGTAAAAC

>NZ_CP009279|7|7|5657172-5657271|CRISPRCasFinder
GTTATTTCAAGCGGAGCCTATGCTTCGTAAAAC	AAAGCGTATGCTTCCGATGTTAGTTTTACGCGAT
GTTATTTCAAGCGGAGCCTATGCTTCGTAAAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042191556.1|5648974_5650660_+|CPBP-family-intramembrane-metalloprotease	unknown	unknown	gnl|CDD|376806
NZ_CP009279.1|WP_143759540.1|5653517_5653673_+|YqzM-family-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191564.1|5657288_5658041_+|heme-dependent-peroxidase	unknown	unknown	gnl|CDD|237033
NZ_CP009279.1|WP_042130884.1|5652841_5653159_-|thioredoxin	unknown	unknown	gnl|CDD|200072
NZ_CP009279.1|WP_036685584.1|5661011_5661155_-|sporulation-histidine-kinase-inhibitor-Sda	unknown	unknown	gnl|CDD|370219
NZ_CP009279.1|WP_042191554.1|5646366_5647035_-|TrkA-family-potassium-uptake-protein	unknown	unknown	gnl|CDD|223643
NZ_CP009279.1|WP_042191571.1|5662463_5662673_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042194483.1|5647048_5648344_-|ATP-synthase-subunit-J	unknown	unknown	gnl|CDD|273349
NZ_CP009279.1|WP_042130890.1|5658380_5659574_-|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224172
NZ_CP009279.1|WP_042191562.1|5654814_5656353_-|helicase-DnaB	unknown	unknown	gnl|CDD|226138
NZ_CP009279.1|WP_042191558.1|5650767_5652735_-|excinuclease-ABC-subunit-UvrC	unknown	unknown	gnl|CDD|234792
NZ_CP009279.1|WP_042191573.1|5662740_5663193_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP009279.1|WP_042191575.1|5663294_5663654_-|iron-sulfur-cluster-assembly-accessory-protein	unknown	unknown	gnl|CDD|223393
NZ_CP009279.1|WP_042191567.1|5658100_5658379_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042130887.1|5656642_5656939_-|hypothetical-protein	unknown	unknown	gnl|CDD|379451
NZ_CP009279.1|WP_042191552.1|5645392_5646295_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP009279.1|WP_094877850.1|5659905_5660880_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223566
NZ_CP009279.1|WP_042191569.1|5661469_5662132_-|hypothetical-protein	unknown	unknown	gnl|CDD|373047
NZ_CP009279.1|WP_042191560.1|5653839_5654796_-|primosomal-protein-DnaI	unknown	unknown	gnl|CDD|236353
NZ_CP009279.1|WP_042191577.1|5664026_5665133_+|aminofutalosine-synthase-MqnE	unknown	unknown	gnl|CDD|213851

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042191556.1|5648974_5650660_+|CPBP-family-intramembrane-metalloprotease	gnl|CDD|376806	pfam02517, Abi, CAAX protease self-immunity. Members of this family are probably proteases (after a isoprenyl group is attached to the Cys residue in the C-terminal CAAX motif of a protein to attach it to the membrane, the AAX tripeptide being removed by one of the CAAX prenyl proteases). The family contains the CAAX prenyl protease. The proteins contain a highly conserved Glu-Glu motif at the amino end of the alignment. The alignment also contains two histidine residues that may be involved in zinc binding. While they are involved in membrane anchoring of proteins in eukaryotes, little is known about their function in prokaryotes. In some known bacteriocin loci, Abi genes have been found downstream of bacteriocin structural genes where they are probably involved in self-immunity. Investigation of the bacteriocin-like loci in the Gram positive bacteria locus from Lactobacillus sakei 23K confirmed that the bacteriocin-like genes (sak23Kalphabeta) exhibited antimicrobial activity when expressed in a heterologous host and that the associated Abi gene (sak23Ki) conferred immunity against the cognate bacteriocin. Interestingly, the immunity genes from three similar systems conferred a high degree of cross-immunity against each other's bacteriocins, suggesting the recognition of a common receptor. Site-directed mutagenesis demonstrated that the conserved motifs constituting the putative proteolytic active site of the Abi proteins are essential for the immunity function of Sak23Ki - thus a new concept in self-immunity.	2.23397e-09
NZ_CP009279.1|WP_094877850.1|5659905_5660880_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	2.00129e-90
NZ_CP009279.1|WP_042191564.1|5657288_5658041_+|heme-dependent-peroxidase	gnl|CDD|237033	PRK12276, PRK12276, putative heme peroxidase; Provisional.	1.06619e-160
NZ_CP009279.1|WP_042191552.1|5645392_5646295_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	5.28367e-47
NZ_CP009279.1|WP_036685584.1|5661011_5661155_-|sporulation-histidine-kinase-inhibitor-Sda	gnl|CDD|370219	pfam08970, Sda, Sporulation inhibitor A. Members of this protein family contain two antiparallel alpha helices that are linked by a highly structured inter-helix loop to form a helical hairpin; the structure is stabilized by numerous hydrophobic and electrostatic interactions. These sporulation inhibitors are antikinases that bind to the histidine kinase KinA phosphotransfer domain and act as a molecular barricade that inhibit productive interaction between the ATP binding site and the phosphorylatable KinA His residue. This results in the inhibition of sporulation (by preventing phosphorylation of spo0A).	2.41765e-08
NZ_CP009279.1|WP_042191554.1|5646366_5647035_-|TrkA-family-potassium-uptake-protein	gnl|CDD|223643	COG0569, TrkA, K+ transport systems, NAD-binding component [Inorganic ion transport and metabolism].	3.18099e-55
NZ_CP009279.1|WP_042194483.1|5647048_5648344_-|ATP-synthase-subunit-J	gnl|CDD|273349	TIGR00933, Trk_system_potassium_uptake_protein_trkH., potassium uptake protein, TrkH family. The proteins of the Trk family are derived from Gram-negative and Gram-positive bacteria, yeast and wheat. The proteins of E. coli K12 TrkH and TrkG as well as several yeast proteins have been functionally characterized.The E. coli TrkH and TrkG proteins are complexed to two peripheral membrane proteins, TrkA, an NAD-binding protein, and TrkE, an ATP-binding protein. This complex forms the potassium uptake system. [Transport and binding proteins, Cations and iron carrying compounds].	1.25927e-102
NZ_CP009279.1|WP_042130890.1|5658380_5659574_-|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	1.40806e-134
NZ_CP009279.1|WP_042191562.1|5654814_5656353_-|helicase-DnaB	gnl|CDD|226138	COG3611, DnaB, Replication initiation/membrane attachment protein [DNA replication, recombination, and repair].	7.95324e-24
NZ_CP009279.1|WP_042191558.1|5650767_5652735_-|excinuclease-ABC-subunit-UvrC	gnl|CDD|234792	PRK00558, uvrC, excinuclease ABC subunit UvrC.	0
NZ_CP009279.1|WP_042191573.1|5662740_5663193_-|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.	9.3126e-16
NZ_CP009279.1|WP_042191575.1|5663294_5663654_-|iron-sulfur-cluster-assembly-accessory-protein	gnl|CDD|223393	COG0316, sufA, Fe-S cluster assembly scaffold protein [Posttranslational modification, protein turnover, chaperones].	8.54174e-46
NZ_CP009279.1|WP_042130887.1|5656642_5656939_-|hypothetical-protein	gnl|CDD|379451	pfam14068, YuiB, Putative membrane protein. This family of bacterial proteins is functionally uncharacterized. Proteins in this family are approximately 100 amino acids in length. There is a conserved FGIGF sequence motif, and many members are putative membrane proteins.	5.03193e-30
NZ_CP009279.1|WP_042130884.1|5652841_5653159_-|thioredoxin	gnl|CDD|200072	TIGR01068, Thioredoxin-like_protein_slr0233, thioredoxin. Several proteins, such as protein disulfide isomerase, have two or more copies of a domain closely related to thioredoxin. This model is designed to recognize authentic thioredoxin, a small protein that should be hit exactly once by this model. Any protein that hits once with a score greater than the second (per domain) trusted cutoff may be taken as thioredoxin. [Energy metabolism, Electron transport].	1.14195e-49
NZ_CP009279.1|WP_042191569.1|5661469_5662132_-|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.	4.86799e-62
NZ_CP009279.1|WP_042191560.1|5653839_5654796_-|primosomal-protein-DnaI	gnl|CDD|236353	PRK08939, PRK08939, primosomal protein DnaI; Reviewed.	7.73578e-89
NZ_CP009279.1|WP_042191577.1|5664026_5665133_+|aminofutalosine-synthase-MqnE	gnl|CDD|213851	TIGR03700, mena_SCO4494, putative menaquinone biosynthesis radical SAM enzyme, SCO4494 family. Members of this protein family appear to be involved in menaquinone biosynthesis by an alternate pathway via futalosine, based on close phylogenetic correlation with known markers of the futalosine pathway, gene clustering in many organisms, and paralogy with the SCO4550 protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	3.83819e-155

Protein sequences

>NZ_CP009279.1|WP_042130887.1|5656642_5656939_-|hypothetical-protein
MGFIPVFILTVLFFVMMFGIGFILNMLMKTTWFPAYLFVLIILPVVVYSIWDRSAMSLWEHLSSFHFVDYLTGVAGLAGAILSGWTIQKLRFGGYKMF
>NZ_CP009279.1|WP_042191562.1|5654814_5656353_-|helicase-DnaB
MRMSNLHHFTEHHRYCVSREFGLSVIDGRMLSSVYQPMVGAFAISFYRLLVEHVPADSIGYSGVEQQRRLFMTLGVEPNEKGRKYLIDQASRLEAVGLLQTCRIYVPETDDYLYEYELMPPLSPADFFATQHLTLLLRDKIGKFAVLSLREQFWNREPEEWSRRSIGKENISVPFYDIFQLNTHVIDYELEQALAEVATVRQPGMRESGEQAIGYSDIILRFPRESVNRAHVEKLRFDHTQMGVINYVAHKYELSPQDLCRLLDEDGVFSPDGEVILDALQYKASQHFRQDMKRQEKREVAAAKVVSIRSSASEENDDSIAPPEQSVEMEYYVEVPPQFLSKCDIHQYNMMLRNEPYTRLLQTFFPGAVPSHLMDMFEKIDLNYKLSGEVINVLIHYLMTMVASGGEQRMNRNFVEAIASNMLVKQVNTYEKAVKYIRDQSKVKGKGATTNTAAGSRSRSYAKNTGRSAKPEIPIVLDDGSAGTVSEEEFAAMMKKAAEIKANKKKGVSQAP
>NZ_CP009279.1|WP_042191560.1|5653839_5654796_-|primosomal-protein-DnaI
MESMGDVLRSINNPTLRQRQRDLEQELFNHPLVKALQSEHPELDDSRLRLHMSRLYQYVEESRHCANCPGLEKCPNDFPGHFSKLTVESVNGSADLYERKTACRLKVAQDNQDSIRKRIRSFYVDERVLNGGYDEIDIMGKDPRRVSAVNKIFDYITSVKEEGLTSRGIYLHGTFGTGKTFLMCYLLHELAVAGYTGVIVYMPDFIEDLKSIMMDGQKMKETVDTLKNCDLLIFDDIGAENLNPWARDHVLGAILNYRMNRKPTFYTSNYPLDGLEKHLSFTSKDGEEIYKGQRLMDRIAPFVDVIPLHGENQRGTIR
>NZ_CP009279.1|WP_143759540.1|5653517_5653673_+|YqzM-family-protein
MDVNAQARDPREHINEEPRNDLGDLMNGFFGMTAFMTVVFFGMVIIKFISE
>NZ_CP009279.1|WP_042130884.1|5652841_5653159_-|thioredoxin
MAIVNVSDQTFSNEVEGQGTVVVDFWAPWCGPCKMIAPILDELSAELGDSVKIAKLNVDENPETASRFGVMSIPTLIFFKDGQPVDKVVGLNSKESLKNIVAKHQ
>NZ_CP009279.1|WP_042191558.1|5650767_5652735_-|excinuclease-ABC-subunit-UvrC
MEGIILDNIRNKLALLPDLPGCYLMKNEEGTIIYVGKAKVLKNRVRSYFTGSHNGKTQRLVANIADFEYIVTSSNMEALILECNLIKKHMPRYNVLLKDDKTFPYIKITNETHPRLEVTRRVIKDKAKYFGPYPNGYAAQQTKKLLDRMYPLRKCGVMPKEVCLYYHMGQCLAPCEKEVQKSEYEQITQDIAAFLSGGHDAVKKDLQQKMQEAAEELYFERAKELRDQIIHIDALMEKQKINTTDTKDRDVFGYAVDKGWMCVQILYMRQGKMIQRHSSVFPFYGEAYSDFMSYVTQYYSDNPALPQEILLPDVLDEEAVVDKEAKPAIVIATPAEEDLQKGEDTPESPEEVEAREMAAAEASAAGVVDAAGGASILQEWLGTKVLVPQRGLKKQMVGMACQNATVAIDEKFRLIERDEVRTSGAAMSLGESLGLERLSRIEAFDNSNIQGTNPVSAMVVFIDGKPARKEYRKYKVRTVVGADDYGTMREVIRRRYERVLKENLPIPDLIVVDGGKGQISSAIDILENELGLFIPVCGLVKDDKHKTAQLLVGDPPEPVALARDSQEFYLLQRIQDEVHRFAITFHREQRGKSMVTSKLDSIPGIGEKRRKALLKHFGSLKKIKEASIEDFKSLSIGEKLASQILEALKDEEPAT
>NZ_CP009279.1|WP_042191556.1|5648974_5650660_+|CPBP-family-intramembrane-metalloprotease
MNPVGQPLQQRALSKRLIISGIIGLILFIMFQIAPSVLNSPAGEDTTVISKAEARDKAISFAEQKLNYTKAPTDQWNVLYDTDSSFYGYMSREKLLEDYTKKKLDQRYPFDIFRVTLSPSAEQEPLISVDLNMYTGAVVAFTQGAEGSGTVLPNNVSTSAKEEDKGTTLSLAQKENLARPWLQEWDVNPAKLQIESNTGNYGLVYTDRSVQIGESLLHYYFDFTGEQVSSFKAGFTAPAWHTSYVKDQTSLAEKFTLFGYGLPTLALGILALIYSILRREHTSFKRGIFLSSAYFVIMMISTYNMLPESSGEGLEAQITSVIMFIIYALYSLLMSSLLYFSLVGGDGLWKKEEGMNPWPRAKEPGYGKYVLDSIRAGYVWAFVLLGVQTLMFIVLSLTLQNWSTTDATQSPYNMRYAWLLPIVAWLAGLSEEAIYRFFGIPMLKKVFRSTFIACLITTLVWAFGHTLYPIYPISSRPIELTVIGLLFSYIFLRYGFIAVMFSHVVFDSILMGATLIFMKESVNVGAGIFAIIMPFIVAYIVYRFNPPQKSEPKPVEPTSVI
>NZ_CP009279.1|WP_042194483.1|5647048_5648344_-|ATP-synthase-subunit-J
MVLGFASIILIGALLLMLPISSTSGNAVSFIDALFTATSATCVTGLVVLDTGTTFTIFGKTVIMVLIQVGGLGFMTMATLFAMMMKRKISLRDRLILQEAMNQGSMEGIVRLIRRVLIYSLVIEGCAAVLLSLRWAFDMPLGKAVYFGIFHAVSMFNNAGFDIFGDFRSLTDYVYDPLVNIVVMFLIVSGGIGFIVMSDLVEFRVKRKLSLHSKVVLSTTAGLILIGALVIFIFEFTNQRTLGNLNFGGKILSAFFQSVSPRTAGANTVDIAGLRQASQFFMVILMFIGASPGSTGGGVKTTTFTIMIGAVIAMLRGREDVVLFRYRLAQERIYKALTLTLLALLLVLTVSMLLSTTEDSNFLAILFETTSAFATVGLTMGLTPELSIFGKILICLTMFAGRLGPLTLVYALGPKQGKPLYKHPEGKIIIG
>NZ_CP009279.1|WP_042191554.1|5646366_5647035_-|TrkA-family-potassium-uptake-protein
MKAQQFVVIGLGRFGSSLALELMEMGYEVLGIDHHEERVEEMSDHLTHAVVADATDEGIMRSLGVRNFDCGIVAIGDNMERSILAAILLKEIGVKQVVAKAISILHGRALSRLGVDRVIFPERDMGIRVAHQLVTPNLLDYIELSKDYKIVELTVPSCMNGKSLSDLNTRAKYGCSIVALNRESGIIVAPTAHDHLSEGDVMVLIGSNESIDRFEDEVVNQD
>NZ_CP009279.1|WP_042191552.1|5645392_5646295_+|LysR-family-transcriptional-regulator
MFDDLDVFAAVVEHSSLNRASRQLNLSQPALSRKISKLEERLGVALFNRYGKRLELTEVGRLTYSYALEQRQQRSKFLEALSKYKEGEPKLVTLGASLTSLQTTLPPLVNAYMEKYPTAELKLITGRTHEIVSSVSEGKSDIGLIASSIQEPGLRCISLFEDQLRLVVSEHHPLNQSTKLTMDDLSRLPMILFSKGTWYRRLTDDLFQRCGIDPDVRMEIDSFEAIVRLLPTVNVAALLPKSYLRPQLLNGGGLVSLHIKELEQTQRTTCLIYRDDGSLSTAARSLVQVTEEMFLTEREK
>NZ_CP009279.1|WP_042191564.1|5657288_5658041_+|heme-dependent-peroxidase
MNEAAMTLEGWYALHDFRSLNWTAWTAADDEERAVALEELHAFMQEWSPVEEAKQGSSAVYSIVGQKADFVMMFLRESLEDLNQLETAFNKIAFAQYTTKAYSYVSIVELSNYLAGGSDGSDPMQNPHVIARLKPVLPQAKHICFYPMNKKRELADNWYMLDMDKRRELMASHGLIGRGYAGKVKQIITGSVGFDDWEWGVTLFAEDPLQFKKLVYEMRFDEVSARYGEFGPFYVGNLLTEDSFEEMLKL
>NZ_CP009279.1|WP_042191567.1|5658100_5658379_-|hypothetical-protein
MRHCSVQVRGLLTREELDRYNGLIEVGSYLEDQNQYDLAYVVQKEIDLLILPGIERLKEKGRARDRATAEYLESLRDDEDDSEEDEEAGTSL
>NZ_CP009279.1|WP_042130890.1|5658380_5659574_-|NAD(P)/FAD-dependent-oxidoreductase
MSSIPKIVILGAGYGGILTAQRLQKALNYNEADVTLVNRHEYHYFTTHLHMPAAGTDSIEHTRVSISKLIDEFKIDLVKSSVQEIRTQQKKIILEDGTLSYDYLVIALGGEPETFGIPGLDKYALTIRSINSVRLIREHIEYQFAKYKNENNAQEHINFVVGGAGFSGIEFVAELADRIPGLCKEFDVDPSMVNIYNIEAAPTALPGFAPELVEYAMNLLTKKGVTFKMGVAIKECLPNGVILASGEEIKASTIVWTGGIRGNRLIEAAGFEAMRGRVKVDEYLRAPGQDNIFIIGDGSLMINPEGRPYPPTAQIAMQQGECCAHNLVAAIRNQQPKKFAFSNKGTVASLGKGQGIAVVGSKTYKGWTAAQLKKVVDMRYLFIIGGIPLVLKKGRFL
>NZ_CP009279.1|WP_094877850.1|5659905_5660880_+|NAD(P)/FAD-dependent-oxidoreductase
MSDLLIIGGGPAGMFAAFYGGMRQASVTLIESMPQLGGQLAALYPEKYIYDVAGFPKVTAQELVDNLTRQMDMFQSNIRLEEKVISVQKRDERHFVVTTDVAEYHSKAIIITAGVGAFEPRRLELPDAGRFEKANLHYFVNDLNAFKDKKVLISGGGDSAVDWALMLEPIAEQVTLIHRRDKFRAHEHSVENLMASKVNVITPTEITELHGDEFITKVTLSHIKTKETQEIEVDSVIVNFGFVSSLGPIAEWGIDIEGNSIVVDSRMETSIPGIFAAGDITTYPGKLKLIAVGFGEAPTAVNNAKVYIDPEAKLSPGHSSNMKL
>NZ_CP009279.1|WP_036685584.1|5661011_5661155_-|sporulation-histidine-kinase-inhibitor-Sda
MVELSDEMLLDSYHRAIELQLEHDFIALLLVEIRKRNLHSPVHAVLH
>NZ_CP009279.1|WP_042191569.1|5661469_5662132_-|hypothetical-protein
MSGRQLASKWLKTEALLSDARVSHYIPMTRVYSADSLLAMLRRYGNVVIKPIVGGGGYGVIKVFRDSRGYGFTYMDRTRIYKDFRSMRRALHFVKVRRKYLIQQGISLARIGGRPIDYRVKVVRNGGVWEFRSMVGRLARPGLFVTNLCKGGTMLSCREGLRRSLPRIKASAKKAEMRRLTLVCIELMERHFPGIGELGFDYAVDYSGKIWILEVNTRPQ
>NZ_CP009279.1|WP_042191571.1|5662463_5662673_+|hypothetical-protein
MAQFFEVLYWVAMLGMSIVLAGTTILICAIGFKFIKDRRRALGAGCIAFSLGAAGLIVFMINYKFIIPA
>NZ_CP009279.1|WP_042191573.1|5662740_5663193_-|GNAT-family-N-acetyltransferase
MLIRKLNAEEQPPLHLLLLADPSLSLVEAYLKRGQCFVAEVENCIIGVYVLLQTRPETVELVNIAVDESQQSKGIGKQLVYHAIQNARLLGAKTIEVGTGNSSIGQLALYQKCGFRITGIDRDFFIRHYSEEIVENGIKVVDMIRLTLDI
>NZ_CP009279.1|WP_042191575.1|5663294_5663654_-|iron-sulfur-cluster-assembly-accessory-protein
MINISEKAAEQLKAMLAEQEVPNMFLRIGVTPGGCSGFSYAMGFDDNETDQDVYMDIQEMKVVVEKENLRYLDGLEIDFEESGMTGGFTINNPNATATCGCGSSFRTATDAGKPNEEPC
>NZ_CP009279.1|WP_042191577.1|5664026_5665133_+|aminofutalosine-synthase-MqnE
MSTLFTPQTDARMMNIIEKVRGGERLNLEDGVYLYQSNDLLTIGQLANEVNLAKNNNRVYFIENMSLYFTNVCESHCAFCNFRKDDGEEGAYTLSGQEMVQYVEQHIHPSVREFHIVGGHNDKVPFQYYVDSLKALNERFPEVTLKAYTAAEIDFFTRISGLSIREVLEQLRAAGLKTLTGGGAEILSDQYRKKMRVDKANVEEYLEVHRTAHQLGMKTHTTMLYGSIESHEDRIRHMMQIRDLQDETNGFMVFIPLSMQPKNKNAGIMRRNSAYEDLKTIAISRLMLDNFDHIKAYFINIGPQLTQVALNFGASDVHGTILKERISHAAGALTPEGLTRDELIWLVKGAGRIPVERDTFYNAIKVYE

Crispr_ID: NZ_CP009279_8

• CRISPR_ID: NZ_CP009279_8
• CRISPR_location: 5902458-5902545
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_8

Consensus_repeat	Method
TAAAACTTACTTCGAAAGCATCC	CRISPRCasFinder

spacers of NZ_CP009279_8

>8.1|5902481|42|NZ_CP009279|CRISPRCasFinder
TGCTTAGTTTTATGAGCATAAGCTTCATTGAATTACTTCGAG

CRISPR arrays and Neighbor proteins around NZ_CP009279_8

CRISPR arrays

The CRISPR arrays of NZ_CP009279_8

>merge|NZ_CP009279|8|5902458-5902545|CRISPRCasFinder
TAAAACTTACTTCGAAAGCATCCTGCTTAGTTTTATGAGCATAAGCTTCATTGAATTACTTCGAGTAAAACTTACTTCGTAAGCATCC

>NZ_CP009279|8|8|5902458-5902545|CRISPRCasFinder
TAAAACTTACTTCGAAAGCATCC	TGCTTAGTTTTATGAGCATAAGCTTCATTGAATTACTTCGAG
TAAAACTTACTTCGTAAGCATCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_CP009279.1|WP_042191876.1|5889045_5890185_-|transglutaminase	unknown	unknown	gnl|CDD|227604
NZ_CP009279.1|WP_042191878.1|5890325_5892698_-|glycoside-hydrolase-family-95-protein	unknown	unknown	gnl|CDD|379625
NZ_CP009279.1|WP_156113187.1|5887137_5887383_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase	unknown	unknown	gnl|CDD|198374
NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|227095
NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase	unknown	unknown	gnl|CDD|235487
NZ_CP009279.1|WP_042191897.1|5905746_5905947_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_076285489.1|5892816_5894574_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein	unknown	unknown	gnl|CDD|239274
NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase	unknown	unknown	gnl|CDD|273540
NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase	unknown	unknown	gnl|CDD|236201
NZ_CP009279.1|WP_042191881.1|5894720_5895626_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP009279.1|WP_042131059.1|5887488_5888967_+|amino-acid-permease	unknown	unknown	gnl|CDD|223903
NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319849
NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase	unknown	unknown	gnl|CDD|234784
NZ_CP009279.1|WP_042191906.1|5914106_5914448_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191903.1|5910215_5911292_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.07434e-65
NZ_CP009279.1|WP_042191876.1|5889045_5890185_-|transglutaminase	gnl|CDD|227604	COG5279, CYK3, Uncharacterized protein involved in cytokinesis, contains TGc (transglutaminase/protease-like) domain [Cell division and chromosome partitioning].	2.24102e-22
NZ_CP009279.1|WP_042191878.1|5890325_5892698_-|glycoside-hydrolase-family-95-protein	gnl|CDD|379625	pfam14498, Glyco_hyd_65N_2, Glycosyl hydrolase family 65, N-terminal domain. This domain represents a domain found to the N-terminus of the glycosyl hydrolase 65 family catalytic domain.	7.11826e-78
NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase	gnl|CDD|198374	cd07808, FGGY_D-XK_EcXK-like, Escherichia coli xylulokinase-like D-xylulose kinases; a subgroup of the FGGY family of carbohydrate kinases. This subgroup is predominantly composed of bacterial D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17), which catalyze the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. D-xylulose has been used as a source of carbon and energy by a variety of microorganisms. Some uncharacterized sequences are also included in this subgroup. The prototypical member of this CD is Escherichia coli xylulokinase (EcXK), which exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. 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 Mg2+ or Mn2+ is required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	0
NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.82715e-83
NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase	gnl|CDD|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_CP009279.1|WP_076285489.1|5892816_5894574_-|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.	0
NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.35147e-133
NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein	gnl|CDD|239274	cd02976, NrdH, NrdH-redoxin (NrdH) family; NrdH is a small monomeric protein with a conserved redox active CXXC motif within a TRX fold, characterized by a glutaredoxin (GRX)-like sequence and TRX-like activity profile. In vitro, it displays protein disulfide reductase activity that is dependent on TRX reductase, not glutathione (GSH). It is part of the NrdHIEF operon, where NrdEF codes for class Ib ribonucleotide reductase (RNR-Ib), an efficient enzyme at low oxygen levels. Under these conditions when GSH is mostly conjugated to spermidine, NrdH can still function and act as a hydrogen donor for RNR-Ib. It has been suggested that the NrdHEF system may be the oldest RNR reducing system, capable of functioning in a microaerophilic environment, where GSH was not yet available. NrdH from Corynebacterium ammoniagenes can form domain-swapped dimers, although it is unknown if this happens in vivo. Domain-swapped dimerization, which results in the blocking of the TRX reductase binding site, could be a mechanism for regulating the oxidation state of the protein.	1.06185e-20
NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	8.3216e-156
NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase	gnl|CDD|236201	PRK08248, PRK08248, homocysteine synthase.	0
NZ_CP009279.1|WP_042191881.1|5894720_5895626_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.57817e-61
NZ_CP009279.1|WP_042131059.1|5887488_5888967_+|amino-acid-permease	gnl|CDD|223903	COG0833, LysP, Amino acid transporters [Amino acid transport and metabolism].	0
NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase	gnl|CDD|319849	cd07551, P-type_ATPase_HM_ZosA_PfeT-like, P-type heavy metal-transporting ATPase, similar to Bacillus subtilis ZosA/PfeT which transports copper, and perhaps zinc under oxidative stress, and perhaps ferrous iron. Bacillus subtilis ZosA/PfeT (previously known as YkvW) transports copper, it may also transport zinc under oxidative stress and may also be involved in ferrous iron efflux. ZosA/PfeT is expressed under the regulation of the peroxide-sensing repressor PerR. It is involved in competence development. Disruption of the zosA/pfeT gene results in low transformability. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.87654e-59
NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase	gnl|CDD|234784	PRK00507, PRK00507, deoxyribose-phosphate aldolase; Provisional.	4.96342e-122

Protein sequences

>NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase
MKYVIGVDLGTSAVKTVLVDPQGKVAFEHSESYPLSRPQPNWSEQNPEDWVKGTLVSLRRLIEVSGIDPSQVDGLSFSGQMHGLVLVDKEGQVLRPAILWNDTRTTAQCRRIEKTLGAKLIEVARNRALEGFTLPKILWIQENEPEVLSQAHQFLLPKDYVRLRLTGDYAMDYSDAAGTLLLDVGSKTWSAEIAEAFELPLSLCPRLVESFEQTGTLLPDIAEASGLLSSTKVFAGGADNACGALGAGVLGEGRTMCSIGTSGVVLSYESNKDLNLEGKVHFFNHGEKDAYYIMGVTLAAGHSLTWFKETFAADKSFDELLSGVASIPAGSGGLLFTPYIVGERTPHPDANIRGSFIGMDSGHTLTHFTRSVLEGITFSLRESIEIVRDSGKEITEIIAIGGGAKNEAWLQMQADIFNASIVKLESEQGPAMGAAMLAAYGSGWFTSLSACAEAFIRPADVYKPDPKQAAIYDGLFNLYQEVYGQTRELNNKLAAYRQ
>NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase
MFQWIVKLLNDIKIRNKLLLAFLLTTLLPVLLVGGYLTFEMRTMAFQSALEQASINVDRVKKRTEEVIGVSQDIAYRLSNDARLKRLAIRQYVSTYDVVEAYRDYSDMREYLRLYKDISNIRLYTDNATLLNNWELINPSPEIKESQWYQRAQRYDSLVGWEYIEDERDKRNYLSLVRKIELEGSSKIGVLVINVNSQQLASILSQESFDTMIVDDQDNIIAANRKDRTGKKLVDVSFDTKLLGQGSGSYEAVVDGEASKIVIEELKPQASRNALRIISVFSIESIVKEPNQVIKLSITVVAISVLLAFLIIYSFSSLFSRRLLHLSRHINRVSTGDFDTTLKIDGKDEIALLARQFNSMVRSINDLMYEVQESNAQNSLLEQKQNDIRFKMLASQINPHFLFNALEAIRMEAHMKGQVEIARVVRLLGKMMRSNLEVGRSKILLSQELEVVRCYLDIQQFRYEERLKYQFTVDPAVESLYMPPLLIQPLVENAVIHGLDNKMEGAFVTVEVVQVGDHAKFTITDNGVGISPIQLEELLNTLERKEEREGERIGLRNVHDRLKLSYGAECGLTIESRPNVGTVIFFCIPMEDNNL
>NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor
MIKVMIVDDEPKLREGLRSLIPWEKLGYTVVATAANGLQALEKYHTFYPELIVADIRMPGMDGLEMISELRKEGSESHVLILSGHADFEYAKRAISYRIDGYLLKPVDEDEMIVCLEQLHETIEQEQRFSDWNEEEPARNRETLLRALLQPTSEEELEEDLSRHVDALGLDQGNYEVILIELRKTAGANDEDLRGIKTVMEQHFSNHPSASFFTLSQYLGILMKDPDQSASKREELYKGLSAVIEPKGYDFIAVAGGLVPRPEMVGESFNSARELLRRSFFFKKGIIISTDPSGFLMEMKEKTEDAQETESRLLLAVETGSLGAIRPIVLTICAELISAGSDELRIKETFVRLLSTVLARLEPTYPEIRTYAAEHSPPIGELYQSYYLSDLQDQAVSFLEEIAGQMTSGRGNEIKKITEIINRRYNENLKLETLSELFCYNSAYLGKMFKNTTGEYFNTYVDKVRIEKAKEFLTQGMKVYEVAEKVGYMNPDYFNAKFRKYVGISPTSYRKSI
>NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease
MKADTVTAQIPPDTRMRNKKPASGGRFWRSFKNQKYLWLMSIPFVIWAFVFSYLPLWGWTMAFQKYKPARGFFEQEWVGFEHFKTLFSDSQFLLALRNTLAMSGMGLVAGFIFPITFAILLNELRLGFFKRFAQTVSYLPHFVSWVVAAGIVTKMLSSENGLVNDLLLTIGFIDSPIQFMAQGHLFWGIVTLSDVWKETGWNAIIYLAAISGIGPELYEAARVDGASRLRQVWHITLPGIRPTITVLLIMSIGNLLNIGFEKQFLLGNNLVTDYSQVLDLYSLKYGLGMARYSYGTAINIFNSVISVILLFTINGIFKRTTKESLL
>NZ_CP009279.1|WP_042191881.1|5894720_5895626_-|carbohydrate-ABC-transporter-permease
MGNTAITGKSWSDRIFDFIVYFVILFVVVITIYPFLNVLAISLNDSVDSVRGGITIYPREFTWDNYLKIFSFAGLITGFKISALRTVVGTLFGLISASMLAFTISRPDFAGRKFVSTFLAMTMYISGGMIPIYMLIKDLHMMNSFAVYVLPGLVSAFNVFVIRSFIDGLPYALQESAKLDGANDFTIYWRVILPLMKPALATIALFLAVGQWNAWFDTYLYNGSSPHLTTLQYELMKVLQSTTSGNGGDYRSNIASLASNQVSPESIKMAITIVVTVPILLVYPFIQKYFVQGMTLGAVKS
>NZ_CP009279.1|WP_076285489.1|5892816_5894574_-|extracellular-solute-binding-protein
MGNNRKIKAKATALTLTSIMMLGMLAGCGGNNGNNAAGDAAGNATNKGNAANSANAVEDTSPLTMTFFSADPNPNWTGMQDEVGKVITEKTGVTLNAEYAVGDPAQKVALIAASGDYPDLISAKTDVSKLVDAGAMLDLTDLIEKYAPNIKKVLGEEGMKRSRYSDDDHAIYAIPTYAGVDNKYFDAGGGFELQHRAVKEAGYPAIKTVQDYENVIKAYLEKHPTDENGNKNIGLTLNADDWYMYITVTNPAFTTTGSPDDGEYAIDIDTQEVTYHFRRPAEKEYFRWLNHMNDIGLLDPESFVQKYDQYKAKIATGRVIGLIDQDWGYGDGERALKAEGKLDQGYGHYPVTLSEEYKETSFWPTGFMGGNGIGISVDAKDPVRAIKFLDYLASDEGQVLVNWGIEGKHYNVVDGKRVIPEDVNNRKYNDTTNFQKETGLGNVGSNYALLSAHYGDGVLDPTGNYYTTRFPEQVTVGYNAVEKETLAAYKATTWKDLFPNEDEFKVKPWGAAWNITIPGDSEIVVLDNKLKDISWKRIPEAILSKPADFDKVWDAYMAELDKAGVTKAEDLREELVKQRVKLWNE
>NZ_CP009279.1|WP_042191878.1|5890325_5892698_-|glycoside-hydrolase-family-95-protein
MGESKNTGVHDLWYKQPAAEWEEALPVGNGRLGGMIFGGTEEELIQLNEDTLWSGFPRDTANYEALRHLTPAKQLVAEGKYKEAEALVDSKMLGRRTESYQPLGDLRMKFNLGGSVEDYQRGLDLDQALATVSYTAGDVRIVREVLASRPDELIVIHIRAEGKEGLGILPDFSVALTSPHPFRLEITPDGALMMTGRAPSHVADNYVGDHPRSVLYEEGLGISFAAAMEIRTDGGKCNAENGMLSVSGARSITIRLAAATDYAGYDRMPGSGGKLPSELCLEQLALSSNGYAELKQRHLEDHQSLFRRVELTLAPSSSRIELPTDEQLARYQEGQADSALEALLFQYGRYLMIAGSRPGTQALNLQGIWNPYLQPPWNSNYTTNINTEMNYWPAELCGLGECHEPLIDFITELSVTGSRTANIHYGARGWTVHHNTDLWRMTSPSDGKAMWAFWPMGGVWLSRHLWERYAFRPDEEYLRNTAYPLLKGAALFCLDWLVELPDGRWTTGLSTSPENVFLTADGTPCSVSAGSAMDLLLIAELFKHCIQAAEILNTDAQLRQELRQKQERLAHPGIAPDGRIREWNEDFAEQEPGHRHVSHLYDLYPGNVISPSFTPELAEAAALSLKKRLEGGGGHTGWSAAWLLNLYARLKDGESAYSCLRRILQDSSLPNLFGNHPPFQIDGNFGTTAGVAEMLLQSHQEGLELLPALPEEWSEGSVKGLIARGGFITNIEWHEGRLTKAELTSTHGQICRIYSHQPLLIQSPDGSRIGIEMEFETVIGETYIITPQSE
>NZ_CP009279.1|WP_042191876.1|5889045_5890185_-|transglutaminase
MWKKRFTLVKIILGGVIIFAAIPPMIYWGWGHAYAASSSPTLRSVNEVAQKLTGAMNNRRETITFTYESKASNLKTKIQAALDQAMASDPYLYYIIDSYGYTYRGSASSVKVTVEVKYLETLEQTAFVNKEVKAALKKIITPGMNNHQKVKAIHDWVVLHLKYDTSYRKYTAYEGLKSGSAVCQGYSLLTYKLLKEAGFTNKIVEGTAKQPGGRSQLHAWNLVLLDGRWYHLDTTWDDPTPDKAGVVSTAYYLRTDAQMRQDHSWTKSYPAASVGYHKTLSALVERGGQNAVVYKQLQKDLNYELYAEELIVRSVGDLTRLANKAIASGEVSILFRYQGSGTKLKNDLQELYKLGLEDVSYSSSAFDNTGDLKVFVTWE
>NZ_CP009279.1|WP_042131059.1|5887488_5888967_+|amino-acid-permease
MQGNQQNPAQGNINQPALKKSFKARHLTMIALGGSIGTGLFLASGGAIASAGPGGALLAYTAVGVMVYFLMTSLGELATYLPDSGSFSTYGTRFVSPAFGFAIGWNFWYNWAVTIAAELSAATVIIKYWFPDSPSFLWSLVFLLLMFGLNFLSARGYGESEYWFAIIKIITVIAFLVVGVLMIFGIMGGEAVGFSNFQIGGSSFHGGFFAFVGVFMAAGFSFQGTELIGVAAGESENPRRNVPIAIRQVFWRILIFYILAIFVIGMLIPYTNPDLLRGGIDDIGVSPFTIVFNKAGLAIAASVMNAVILSSVLSAGNSGMYASTRVLYAMAKDGMAPRALGKLNRRGVPVGALLVTTAVGMLAFLASFFGDGAVYNWLLNASGMCGFINWLGIAVCHYRFRRAFIAQGHSLDELPYRARWFPFGPIFALGLCIVAILGQNMGAFSGGNIDWYGIAVSYISLPLFVLIWVGYRWFRKSNIIPLDKCDLSTHPE
>NZ_CP009279.1|WP_156113187.1|5887137_5887383_-|hypothetical-protein
MDDCTKHTNSVNAKKPQTMSAASIYTAPHHTPCEDSATHCSLLLTQAVQCDSSVPFGNGPSLHRCKSYSASFGGYSFRRDS
>NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase
MAYFETVNKISYEGSRSTNPFAFKFYNPKEVVAGKTMEEHLKFAMAYWHTLTAGGSDPFGAETAIRSWNKLNGLDKAKARAEAAFEFMDKMDLPYFCFHDVDIAPEGASLREFYSNIDTIVDILEQGMKTSGKKLLWNTANMFTNPRYMHGAGSTPNADVFAHAAAQVKKGLEVGKRLGASNYVFWGGREGYEELLNTDMGLEQDNIARLFSMAVDYAKEIGFDGQFLIEPKPKEPTKHQYDFDAATTISFLQKYNLDKHFKLNLEANHATLAGHTFEHELRVARINGMLGSLDANQGDTLLGWDTDEFPVNIYDATLTLYEVLKNDGLGKGGINFDSKVRRPSFEPEDLFLAHIAGMDTYAKGLKVAAKLIEDRVFEDFVEKRYSSFNEGVGADIVSGKATLASLAEYALNNENPRPNQSGRQEYLRATLNQYILAE
>NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator
MKVTGDQALVKKINKSIVLHTIRRHSPLSRAKVSEMTGLNKATVSNLVAELCTQELVTEVGPGESSGGRKPLMLHFNTMAGSVIGIELRVKQLTAVLCDLSGGILYESDFSLENHDFPYVLEQMKKLISGLIINAPESPYGIVGIGVGVPGMVDENGVVLFAPNLGWEMVELRAILEAEFSVPVTIDNEANAGAQGELNFGAAREVRHLLYISAGSGIGSGIIIGGELYKGARGYAGETGHMTIEAQGKPCSCGSRGCWELYASEKTYDNPDLSLPAHTTPELVRYAAGGQEDALHHFSTMGEYLGIGVTNLINSFNPELIVIGGALSEAEEWLGKPLRRVVAERTLPYHKQQLEITFSKLGSRGTMIGAGFSAVMHFLGDIRVTL
>NZ_CP009279.1|WP_042191897.1|5905746_5905947_+|hypothetical-protein
MTYVDTSDISAQMFITVLLFLLIIAPLISLGVLRFFQAKKKSGFILIGSGAAVYVLFQLITSFTQT
>NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein
MENVIVYTSTNCPHCRQVKSFLSEKGVSYEERNVEQNDDFAQQVWDMGVRAIPVTVIGEHKIVGMNKTQFDKALATV
>NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase
MYKSIIVGTGPAGLTAAIYLARANLNPLVIEGPQPGGQLTTTTEVENFPGFPEGIMGPDLMDNMRKQAERFGAEFRTGWVNSVELGERPFKLNVEGMGVLTTDTLIISTGATAKYLGIPGEQDNVGRGVSTCATCDGFFFRNKEIVVVGGGDSALEEAGFLTRFASKVTLVHRRGELRASKIMQDRVRANVKVDWNLNRTPLEVTSSERGVNGLKVLNNETGEEEIIEASGVFVAIGHHPNTSFLGGQITTNADGYIMTNPGTSETNIPGVFACGDVQDTRYRQAITAAGSGCMAAMDAEKYIESLEHSAVIL
>NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase
MQVTSKHLPKQKSISGSMKKPGAPKRRFDPRAMLSNSEMQAALGSGLLMLFAWSVSGWSEILSIALYVISYTIGGWNKAKEGVETLVKERDLDVNLLMIAAALGAASIGYWNEGAMLIFIFALSGALESYTMERSKKDISSLMALKPATAMRIEKGSMNEVNIDQLVIGDLLLVRPGDLIPADGKVYRGESAVDQASITGESVPVEKCAGSEVFAGTVNGEGPLYIEVTKAAENTLFAKIIKMVEEAETEVPNSQRFIKRLEAIYARVVVASTVALIILPPFLLDWSWSATFYKAMVFLVVASPCALVSSIMPAMLSAISKSARKGVLFKGGVHLENMARTTVVAFDKTGTLTEGTPQVTDFIAGEGYSRQELLTVSASIEHMSRHPLAEAIVRKAEEEGLALQGVEDSKTITGWGIEGQIDGHLWRIGKSNLLDELTPSAMNPELEHWKLKRQQLAEEGKTVSIILDGEQIAGMIALQDTVRPQAEAAVRKLQELGIKVAMLTGDRDATAQVIAGTTGVDMVFADLLPEDKVKHIKALREKYGHVVMVGDGVNDAPALATATVGMGMGMKGSGAALEIADVVLMNDNIEEIASTISLARRSQRIVKQNMIFAVTVIAVLMISNFVQGIALPFGVIGHEGSTILVILNGLRLLR
>NZ_CP009279.1|WP_042191903.1|5910215_5911292_-|hypothetical-protein
MKGERQQDGFRSSEERPFKFMYKAGDRAVGMEMSQAGSVASAAAEFITGVEQKDVVEPLNRSYFKRPGEQSAFLVLREGREEREERPITREGARSVQAGPCLIRSEEWLLEPELFCLYEHWLSSEDELQANRMLQRIYYRLQAATTALLESPDGEWAAVTLLHPEELAAQPAKLAALQDAQLEALFTAVAESQRQGGDCRLDLLVAYTASGAEFAAKREFIEVVADQTLGHAYAAACRIGALIAPDVEPSAAAEIARIADFLVLDGAASELAPEGAAAEGFTLAAGEILAAVRSVKPAAVVLAAGTPAASALADLYQIGLSGIFCSAGQRTEALLRAACLIWIARQQETLDTAAGGRQ
>NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase
MSEDRKLSFETLTVHAGQEIDPTTFARAVPLYQTTSYGFRDADHAADLFALKEFGNIYTRLMNPTTDVFEQRLAALEGGAGALATASGAAAISFSILNIAGAGDEIVSAASLYGGTYNLFSTTLPKLGIKVHFVDSDNPENFRAAINDKTKALYAETIGNPQGNVLDIEAVAAIAHEHGIPLIVDNTFPSPYLLRPIEHGADIVVHSATKFIGGHGTSIGGIIVDGGKFDWKASGKFPGLTEPDPSYHGVVYTEAVGPIAYIIKARVQLLRDLGASISPFNSWMLLQGLETLHLRMERHSQNALKVAQYLEAHADVEWVSYSGLPTHPSHELAQKYLPKGQGAILTFGIKGGSAAGRKLIENVKLFSHLANVGDSKSLIIHPASTTHAQLSDEEQTTAGVTPELLRLSIGTESIDDIIYDLEQAIAASQQ
>NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase
MSEITLSRIIDHTLLKADARKEDIVKLAEEAKAYKFASVCVNPAWVATAHEVLKDTPEVKVCTVIGFPLGSSTTETKAFETTNAIANGAGEVDMVINIGALKDGNNELVKRDIAAVVDAARGKALTKVIIETCLLTEEEKVRACKLSVEAGADFVKTSTGFSTGGATKEDIALMRATVGPNVGVKASGGVRSAEDAHVMVQAGASRIGTSGGVAIAKGETSQSNY
>NZ_CP009279.1|WP_042191906.1|5914106_5914448_+|hypothetical-protein
MGNFNFTSNAAAQKLNVQVEGSMSPEDAGRFIQEYNQIVSTFDPAQYEIILDCKTLNVSSPDTLPMLEQCYILYKESGFKKVTFIIAKSPVLKMQLSRVARATKLENYEIIEA

Crispr_ID: NZ_CP009279_9

• CRISPR_ID: NZ_CP009279_9
• CRISPR_location: 5909649-5909743
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_9

Consensus_repeat	Method
TTCGTGAGCATACGCTTTGTTTTGTGGAG	CRISPRCasFinder

spacers of NZ_CP009279_9

>9.1|5909678|37|NZ_CP009279|CRISPRCasFinder
CCTAACTTCATTGGTTTTTCTTCGAAACAAAACTTAG

CRISPR arrays and Neighbor proteins around NZ_CP009279_9

CRISPR arrays

The CRISPR arrays of NZ_CP009279_9

>merge|NZ_CP009279|9|5909649-5909743|CRISPRCasFinder
TTCGTGAGCATACGCTTTGTTTTGTGGAGCCTAACTTCATTGGTTTTTCTTCGAAACAAAACTTAGTTCGTGAGCATACGCTCTGTTTTGTGGAG

>NZ_CP009279|9|9|5909649-5909743|CRISPRCasFinder
TTCGTGAGCATACGCTTTGTTTTGTGGAG	CCTAACTTCATTGGTTTTTCTTCGAAACAAAACTTAG
TTCGTGAGCATACGCTCTGTTTTGTGGAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_CP009279.1|WP_042191897.1|5905746_5905947_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_156113247.1|5914545_5915451_+|ketoacyl-ACP-synthase-III	unknown	unknown	gnl|CDD|223409
NZ_CP009279.1|WP_042191918.1|5919139_5920582_-|SulP-family-inorganic-anion-transporter	unknown	unknown	gnl|CDD|223732
NZ_CP009279.1|WP_042191916.1|5918469_5918952_-|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|273242
NZ_CP009279.1|WP_042191906.1|5914106_5914448_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191914.1|5917449_5918448_-|LLM-class-flavin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274646
NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase	unknown	unknown	gnl|CDD|198374
NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|227095
NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase	unknown	unknown	gnl|CDD|235487
NZ_CP009279.1|WP_042191903.1|5910215_5911292_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein	unknown	unknown	gnl|CDD|239274
NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase	unknown	unknown	gnl|CDD|273540
NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase	unknown	unknown	gnl|CDD|236201
NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319849
NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP009279.1|WP_052404520.1|5915547_5916369_-|prohibitin-family-protein	unknown	unknown	gnl|CDD|259799
NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase	unknown	unknown	gnl|CDD|234784
NZ_CP009279.1|WP_042191912.1|5916486_5917260_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.07434e-65
NZ_CP009279.1|WP_156113247.1|5914545_5915451_+|ketoacyl-ACP-synthase-III	gnl|CDD|223409	COG0332, FabH, 3-oxoacyl-[acyl-carrier-protein].	6.93955e-72
NZ_CP009279.1|WP_042191914.1|5917449_5918448_-|LLM-class-flavin-dependent-oxidoreductase	gnl|CDD|274646	TIGR03558, oxido_grp_1, luciferase family oxidoreductase, group 1. The Pfam domain family pfam00296 is named for luciferase-like monooxygenases, but the family also contains several coenzyme F420-dependent enzymes. This protein family represents a well-resolved clade within family pfam00296 and shows no restriction to coenzyme F420-positive species, unlike some other clades within pfam00296. [Unknown function, Enzymes of unknown specificity].	3.6746e-114
NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase	gnl|CDD|198374	cd07808, FGGY_D-XK_EcXK-like, Escherichia coli xylulokinase-like D-xylulose kinases; a subgroup of the FGGY family of carbohydrate kinases. This subgroup is predominantly composed of bacterial D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17), which catalyze the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. D-xylulose has been used as a source of carbon and energy by a variety of microorganisms. Some uncharacterized sequences are also included in this subgroup. The prototypical member of this CD is Escherichia coli xylulokinase (EcXK), which exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. 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 Mg2+ or Mn2+ is required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	0
NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.82715e-83
NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase	gnl|CDD|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_CP009279.1|WP_042191916.1|5918469_5918952_-|Rrf2-family-transcriptional-regulator	gnl|CDD|273242	TIGR00738, Putative_HTH-type_transcriptional_regulator, Rrf2 family protein. This model represents a superfamily of probable transcriptional regulators. One member, RRF2 of Desulfovibrio vulgaris is an apparent regulatory protein experimentally (MEDLINE:97293189). The N-terminal region appears related to the DNA-binding biotin repressor region of the BirA bifunctional according to results after three rounds of PSI-BLAST with a fairly high stringency. [Unknown function, General].	1.73794e-28
NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein	gnl|CDD|239274	cd02976, NrdH, NrdH-redoxin (NrdH) family; NrdH is a small monomeric protein with a conserved redox active CXXC motif within a TRX fold, characterized by a glutaredoxin (GRX)-like sequence and TRX-like activity profile. In vitro, it displays protein disulfide reductase activity that is dependent on TRX reductase, not glutathione (GSH). It is part of the NrdHIEF operon, where NrdEF codes for class Ib ribonucleotide reductase (RNR-Ib), an efficient enzyme at low oxygen levels. Under these conditions when GSH is mostly conjugated to spermidine, NrdH can still function and act as a hydrogen donor for RNR-Ib. It has been suggested that the NrdHEF system may be the oldest RNR reducing system, capable of functioning in a microaerophilic environment, where GSH was not yet available. NrdH from Corynebacterium ammoniagenes can form domain-swapped dimers, although it is unknown if this happens in vivo. Domain-swapped dimerization, which results in the blocking of the TRX reductase binding site, could be a mechanism for regulating the oxidation state of the protein.	1.06185e-20
NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	8.3216e-156
NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase	gnl|CDD|236201	PRK08248, PRK08248, homocysteine synthase.	0
NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.35147e-133
NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase	gnl|CDD|319849	cd07551, P-type_ATPase_HM_ZosA_PfeT-like, P-type heavy metal-transporting ATPase, similar to Bacillus subtilis ZosA/PfeT which transports copper, and perhaps zinc under oxidative stress, and perhaps ferrous iron. Bacillus subtilis ZosA/PfeT (previously known as YkvW) transports copper, it may also transport zinc under oxidative stress and may also be involved in ferrous iron efflux. ZosA/PfeT is expressed under the regulation of the peroxide-sensing repressor PerR. It is involved in competence development. Disruption of the zosA/pfeT gene results in low transformability. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.87654e-59
NZ_CP009279.1|WP_052404520.1|5915547_5916369_-|prohibitin-family-protein	gnl|CDD|259799	cd03401, SPFH_prohibitin, Prohibitin family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model characterizes proteins similar to prohibitin (a lipid raft-associated integral membrane protein). Individual proteins of the SPFH (band 7) domain superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. These microdomains, in addition to being stable scaffolds, may also be dynamic units with their own regulatory functions. Prohibitin is a mitochondrial inner-membrane protein which may act as a chaperone for the stabilization of mitochondrial proteins. Human prohibitin forms a hetero-oligomeric complex with Bap-37 (prohibitin 2, an SPFH domain carrying homolog). This complex may protect non-assembled membrane proteins against proteolysis by the m-AAA protease. Prohibitin and Bap-37 yeast homologs have been implicated in yeast longevity and in the maintenance of mitochondrial morphology.	6.18435e-69
NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase	gnl|CDD|234784	PRK00507, PRK00507, deoxyribose-phosphate aldolase; Provisional.	4.96342e-122
NZ_CP009279.1|WP_042191918.1|5919139_5920582_-|SulP-family-inorganic-anion-transporter	gnl|CDD|223732	COG0659, SUL1, Sulfate permease and related transporters (MFS superfamily) [Inorganic ion transport and metabolism].	5.06241e-132

Protein sequences

>NZ_CP009279.1|WP_081951213.1|5907614_5909579_-|cadmium-translocating-P-type-ATPase
MQVTSKHLPKQKSISGSMKKPGAPKRRFDPRAMLSNSEMQAALGSGLLMLFAWSVSGWSEILSIALYVISYTIGGWNKAKEGVETLVKERDLDVNLLMIAAALGAASIGYWNEGAMLIFIFALSGALESYTMERSKKDISSLMALKPATAMRIEKGSMNEVNIDQLVIGDLLLVRPGDLIPADGKVYRGESAVDQASITGESVPVEKCAGSEVFAGTVNGEGPLYIEVTKAAENTLFAKIIKMVEEAETEVPNSQRFIKRLEAIYARVVVASTVALIILPPFLLDWSWSATFYKAMVFLVVASPCALVSSIMPAMLSAISKSARKGVLFKGGVHLENMARTTVVAFDKTGTLTEGTPQVTDFIAGEGYSRQELLTVSASIEHMSRHPLAEAIVRKAEEEGLALQGVEDSKTITGWGIEGQIDGHLWRIGKSNLLDELTPSAMNPELEHWKLKRQQLAEEGKTVSIILDGEQIAGMIALQDTVRPQAEAAVRKLQELGIKVAMLTGDRDATAQVIAGTTGVDMVFADLLPEDKVKHIKALREKYGHVVMVGDGVNDAPALATATVGMGMGMKGSGAALEIADVVLMNDNIEEIASTISLARRSQRIVKQNMIFAVTVIAVLMISNFVQGIALPFGVIGHEGSTILVILNGLRLLR
>NZ_CP009279.1|WP_042191901.1|5906516_5907458_-|thioredoxin-disulfide-reductase
MYKSIIVGTGPAGLTAAIYLARANLNPLVIEGPQPGGQLTTTTEVENFPGFPEGIMGPDLMDNMRKQAERFGAEFRTGWVNSVELGERPFKLNVEGMGVLTTDTLIISTGATAKYLGIPGEQDNVGRGVSTCATCDGFFFRNKEIVVVGGGDSALEEAGFLTRFASKVTLVHRRGELRASKIMQDRVRANVKVDWNLNRTPLEVTSSERGVNGLKVLNNETGEEEIIEASGVFVAIGHHPNTSFLGGQITTNADGYIMTNPGTSETNIPGVFACGDVQDTRYRQAITAAGSGCMAAMDAEKYIESLEHSAVIL
>NZ_CP009279.1|WP_042191899.1|5906213_5906447_-|glutaredoxin-family-protein
MENVIVYTSTNCPHCRQVKSFLSEKGVSYEERNVEQNDDFAQQVWDMGVRAIPVTVIGEHKIVGMNKTQFDKALATV
>NZ_CP009279.1|WP_042191897.1|5905746_5905947_+|hypothetical-protein
MTYVDTSDISAQMFITVLLFLLIIAPLISLGVLRFFQAKKKSGFILIGSGAAVYVLFQLITSFTQT
>NZ_CP009279.1|WP_042191895.1|5904370_5905531_+|ROK-family-transcriptional-regulator
MKVTGDQALVKKINKSIVLHTIRRHSPLSRAKVSEMTGLNKATVSNLVAELCTQELVTEVGPGESSGGRKPLMLHFNTMAGSVIGIELRVKQLTAVLCDLSGGILYESDFSLENHDFPYVLEQMKKLISGLIINAPESPYGIVGIGVGVPGMVDENGVVLFAPNLGWEMVELRAILEAEFSVPVTIDNEANAGAQGELNFGAAREVRHLLYISAGSGIGSGIIIGGELYKGARGYAGETGHMTIEAQGKPCSCGSRGCWELYASEKTYDNPDLSLPAHTTPELVRYAAGGQEDALHHFSTMGEYLGIGVTNLINSFNPELIVIGGALSEAEEWLGKPLRRVVAERTLPYHKQQLEITFSKLGSRGTMIGAGFSAVMHFLGDIRVTL
>NZ_CP009279.1|WP_042131068.1|5902677_5903994_-|xylose-isomerase
MAYFETVNKISYEGSRSTNPFAFKFYNPKEVVAGKTMEEHLKFAMAYWHTLTAGGSDPFGAETAIRSWNKLNGLDKAKARAEAAFEFMDKMDLPYFCFHDVDIAPEGASLREFYSNIDTIVDILEQGMKTSGKKLLWNTANMFTNPRYMHGAGSTPNADVFAHAAAQVKKGLEVGKRLGASNYVFWGGREGYEELLNTDMGLEQDNIARLFSMAVDYAKEIGFDGQFLIEPKPKEPTKHQYDFDAATTISFLQKYNLDKHFKLNLEANHATLAGHTFEHELRVARINGMLGSLDANQGDTLLGWDTDEFPVNIYDATLTLYEVLKNDGLGKGGINFDSKVRRPSFEPEDLFLAHIAGMDTYAKGLKVAAKLIEDRVFEDFVEKRYSSFNEGVGADIVSGKATLASLAEYALNNENPRPNQSGRQEYLRATLNQYILAE
>NZ_CP009279.1|WP_042191893.1|5900908_5902405_-|xylulokinase
MKYVIGVDLGTSAVKTVLVDPQGKVAFEHSESYPLSRPQPNWSEQNPEDWVKGTLVSLRRLIEVSGIDPSQVDGLSFSGQMHGLVLVDKEGQVLRPAILWNDTRTTAQCRRIEKTLGAKLIEVARNRALEGFTLPKILWIQENEPEVLSQAHQFLLPKDYVRLRLTGDYAMDYSDAAGTLLLDVGSKTWSAEIAEAFELPLSLCPRLVESFEQTGTLLPDIAEASGLLSSTKVFAGGADNACGALGAGVLGEGRTMCSIGTSGVVLSYESNKDLNLEGKVHFFNHGEKDAYYIMGVTLAAGHSLTWFKETFAADKSFDELLSGVASIPAGSGGLLFTPYIVGERTPHPDANIRGSFIGMDSGHTLTHFTRSVLEGITFSLRESIEIVRDSGKEITEIIAIGGGAKNEAWLQMQADIFNASIVKLESEQGPAMGAAMLAAYGSGWFTSLSACAEAFIRPADVYKPDPKQAAIYDGLFNLYQEVYGQTRELNNKLAAYRQ
>NZ_CP009279.1|WP_042191891.1|5898903_5900691_-|sensor-histidine-kinase
MFQWIVKLLNDIKIRNKLLLAFLLTTLLPVLLVGGYLTFEMRTMAFQSALEQASINVDRVKKRTEEVIGVSQDIAYRLSNDARLKRLAIRQYVSTYDVVEAYRDYSDMREYLRLYKDISNIRLYTDNATLLNNWELINPSPEIKESQWYQRAQRYDSLVGWEYIEDERDKRNYLSLVRKIELEGSSKIGVLVINVNSQQLASILSQESFDTMIVDDQDNIIAANRKDRTGKKLVDVSFDTKLLGQGSGSYEAVVDGEASKIVIEELKPQASRNALRIISVFSIESIVKEPNQVIKLSITVVAISVLLAFLIIYSFSSLFSRRLLHLSRHINRVSTGDFDTTLKIDGKDEIALLARQFNSMVRSINDLMYEVQESNAQNSLLEQKQNDIRFKMLASQINPHFLFNALEAIRMEAHMKGQVEIARVVRLLGKMMRSNLEVGRSKILLSQELEVVRCYLDIQQFRYEERLKYQFTVDPAVESLYMPPLLIQPLVENAVIHGLDNKMEGAFVTVEVVQVGDHAKFTITDNGVGISPIQLEELLNTLERKEEREGERIGLRNVHDRLKLSYGAECGLTIESRPNVGTVIFFCIPMEDNNL
>NZ_CP009279.1|WP_042191888.1|5897365_5898907_-|response-regulator-transcription-factor
MIKVMIVDDEPKLREGLRSLIPWEKLGYTVVATAANGLQALEKYHTFYPELIVADIRMPGMDGLEMISELRKEGSESHVLILSGHADFEYAKRAISYRIDGYLLKPVDEDEMIVCLEQLHETIEQEQRFSDWNEEEPARNRETLLRALLQPTSEEELEEDLSRHVDALGLDQGNYEVILIELRKTAGANDEDLRGIKTVMEQHFSNHPSASFFTLSQYLGILMKDPDQSASKREELYKGLSAVIEPKGYDFIAVAGGLVPRPEMVGESFNSARELLRRSFFFKKGIIISTDPSGFLMEMKEKTEDAQETESRLLLAVETGSLGAIRPIVLTICAELISAGSDELRIKETFVRLLSTVLARLEPTYPEIRTYAAEHSPPIGELYQSYYLSDLQDQAVSFLEEIAGQMTSGRGNEIKKITEIINRRYNENLKLETLSELFCYNSAYLGKMFKNTTGEYFNTYVDKVRIEKAKEFLTQGMKVYEVAEKVGYMNPDYFNAKFRKYVGISPTSYRKSI
>NZ_CP009279.1|WP_042191885.1|5895691_5896672_-|sugar-ABC-transporter-permease
MKADTVTAQIPPDTRMRNKKPASGGRFWRSFKNQKYLWLMSIPFVIWAFVFSYLPLWGWTMAFQKYKPARGFFEQEWVGFEHFKTLFSDSQFLLALRNTLAMSGMGLVAGFIFPITFAILLNELRLGFFKRFAQTVSYLPHFVSWVVAAGIVTKMLSSENGLVNDLLLTIGFIDSPIQFMAQGHLFWGIVTLSDVWKETGWNAIIYLAAISGIGPELYEAARVDGASRLRQVWHITLPGIRPTITVLLIMSIGNLLNIGFEKQFLLGNNLVTDYSQVLDLYSLKYGLGMARYSYGTAINIFNSVISVILLFTINGIFKRTTKESLL
>NZ_CP009279.1|WP_042191903.1|5910215_5911292_-|hypothetical-protein
MKGERQQDGFRSSEERPFKFMYKAGDRAVGMEMSQAGSVASAAAEFITGVEQKDVVEPLNRSYFKRPGEQSAFLVLREGREEREERPITREGARSVQAGPCLIRSEEWLLEPELFCLYEHWLSSEDELQANRMLQRIYYRLQAATTALLESPDGEWAAVTLLHPEELAAQPAKLAALQDAQLEALFTAVAESQRQGGDCRLDLLVAYTASGAEFAAKREFIEVVADQTLGHAYAAACRIGALIAPDVEPSAAAEIARIADFLVLDGAASELAPEGAAAEGFTLAAGEILAAVRSVKPAAVVLAAGTPAASALADLYQIGLSGIFCSAGQRTEALLRAACLIWIARQQETLDTAAGGRQ
>NZ_CP009279.1|WP_042131076.1|5911501_5912794_-|homocysteine-synthase
MSEDRKLSFETLTVHAGQEIDPTTFARAVPLYQTTSYGFRDADHAADLFALKEFGNIYTRLMNPTTDVFEQRLAALEGGAGALATASGAAAISFSILNIAGAGDEIVSAASLYGGTYNLFSTTLPKLGIKVHFVDSDNPENFRAAINDKTKALYAETIGNPQGNVLDIEAVAAIAHEHGIPLIVDNTFPSPYLLRPIEHGADIVVHSATKFIGGHGTSIGGIIVDGGKFDWKASGKFPGLTEPDPSYHGVVYTEAVGPIAYIIKARVQLLRDLGASISPFNSWMLLQGLETLHLRMERHSQNALKVAQYLEAHADVEWVSYSGLPTHPSHELAQKYLPKGQGAILTFGIKGGSAAGRKLIENVKLFSHLANVGDSKSLIIHPASTTHAQLSDEEQTTAGVTPELLRLSIGTESIDDIIYDLEQAIAASQQ
>NZ_CP009279.1|WP_143759565.1|5913106_5913784_-|deoxyribose-phosphate-aldolase
MSEITLSRIIDHTLLKADARKEDIVKLAEEAKAYKFASVCVNPAWVATAHEVLKDTPEVKVCTVIGFPLGSSTTETKAFETTNAIANGAGEVDMVINIGALKDGNNELVKRDIAAVVDAARGKALTKVIIETCLLTEEEKVRACKLSVEAGADFVKTSTGFSTGGATKEDIALMRATVGPNVGVKASGGVRSAEDAHVMVQAGASRIGTSGGVAIAKGETSQSNY
>NZ_CP009279.1|WP_042191906.1|5914106_5914448_+|hypothetical-protein
MGNFNFTSNAAAQKLNVQVEGSMSPEDAGRFIQEYNQIVSTFDPAQYEIILDCKTLNVSSPDTLPMLEQCYILYKESGFKKVTFIIAKSPVLKMQLSRVARATKLENYEIIEA
>NZ_CP009279.1|WP_156113247.1|5914545_5915451_+|ketoacyl-ACP-synthase-III
MGKDIKRFLEVMGRDRRYIVNDKDENALTMGLKAAQKALQEANLQGEDMDMIMFASQTPEYTYPTNALLLHHMLHGKHRTITQDSNANCAGMVSAVEQTSRYMQANPSIRYALVVGSDYSSVHCNTDDEITYPNFGDAAAAVILERSGEQSGFIDSLYYTDSEGSENIMFPACGLSNIYHEDITPEQIRIRWTPFDGTVCVNAAVADMKELLSRNGLTTDDISAFCLSQFSLKNIELIQEGLGLTDEKFIYVGDEFGYTATSSPFIAFQRGVEDGRIKRGDYVFFWSVGAGWQIPTMLYQY
>NZ_CP009279.1|WP_052404520.1|5915547_5916369_-|prohibitin-family-protein
MNPKLKQLRPGKIVSGVAAVLIVLLIGANSFVSVEYGHVGLYKTFGKLNDNTLSPGIHFKVPFIQTVIQVNTQVTKAETDTSASSKDLQPVSTHVAVNYSVNKASAFNLMNNIGGNFDNVIINPAIQEIVKEVTAKYPAEDLITRRDVVSSEISEHLTARLAKYDLIVNDINIVNFKFSEAFNQSIEAKQVAQQQALKAENDLRRIEIEAKQKIAQAQAEAESLRLKKQEVTPELVQLKQIEVQEKALEKWNGVLPSVTGGATPFVDVQSLTK
>NZ_CP009279.1|WP_042191912.1|5916486_5917260_-|hypothetical-protein
MFPLHKSVTLTALLLMNLLAGCQHQVDPTPLQSANDYHTSRPKPTDTSANLIKLEWMLVDTIPVVSQLSAPPTGATLITEKKLNNFGGVKVKVYTMVSDEDYVYAKISTSKGQYSLGAIGTYNYRQPEDIKVEVVGIFSEKVLKITGGLGANNSLTNYYLIDESGNPSGLLQIDTGHSNELDVDGDGSIEGVAAHGNPMSAYIYRWNVDHAEVTYVNDALKADSVVLTYEGIYEAFNIGDKQSKRFRLTLEGLIQER
>NZ_CP009279.1|WP_042191914.1|5917449_5918448_-|LLM-class-flavin-dependent-oxidoreductase
MRLSVLDQAPVTSGNTAEGALNKAEELAILADELGYSRMWMAEHHGGNTFASSAPEVTAARLAAKTNRIRIGTGGVMMMHYSPLKLAEVFKTLSAFTPGRIDFGVGRAPGGDTSAMYALSEGRELMLHNMYDKLGITMQLLSDQIPESELYAKNLAAPTKVALPEVWLLGSSGNSARKAAQMGVGYSFAQFFNGAMSNEILDEYRNNYQPSIFMDKPEISVSYMVTTAETKEEAEYEALPQDIFRLMMSKGRITQVLTPEEAQNISLSEIDRMSIKESRKIHLVGAVKDIAVRLQEEQAQYGFQEAMICSIPHSQEKRLEVYRLLARELLGS
>NZ_CP009279.1|WP_042191916.1|5918469_5918952_-|Rrf2-family-transcriptional-regulator
MHMKTGVEQSVYALVLLNMLPDKAVLSGEAISQQLGASATYFQKLLRKLVTADIITSVPGIKGGFKLKKRPEDIRVYDVYLAVEGQQSLYSSNGILVDMLDLEKEDSCCLLTNLMEEAESSWKAVLKRETIASLSEEMRGERFKDKIAALEEWISNKMVI
>NZ_CP009279.1|WP_042191918.1|5919139_5920582_-|SulP-family-inorganic-anion-transporter
MLKQLTLNNGWFSNTRTDILSGMTVAVALIPEAIAFSILAGVSPMVGLYASFCIAIVTALAGGRPGMISAATGAMALLVGSLVLEHGIEYLFAATVLAGVFQILMGMLKLGRFITFLPQPVMTGFVNALAILIFMAQFTHFKGQGWVMYGLVALTLLIIYTVPRFTKAVPSALVAIVIVSILSIALHLDVRTVGDMGNITATLPLFHLPQIPFTLDTLLIILPYSLSLAVVGLLESLMTATLIDDITGTGSDKNREAKGQGLANVVTGFFGGMAGCAMIGQSMFNMKSGGRTRLSTFVSGIFLLFLIIVLGDVVKQIPMGALVGVMIMVCISTFEWGSLKSLTRVPLSDALVMIVTVVTVVATDNLSIGVLFGVLLSALTFAWKIASIRLTVQEAASSKTYAVTGQLFFGTTSHFIHEFAYDSDPDHIIIDFSHSHVWDQSAVHAIAKTMSKYAVRGKKVTITGLNDQSSQLVQRVGLSI

Crispr_ID: NZ_CP009279_10

• CRISPR_ID: NZ_CP009279_10
• CRISPR_location: 6082990-6083082
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP009279_10

Consensus_repeat	Method
CTTCGTACAAAACTCACTTCGGAAGCAT	CRISPRCasFinder

spacers of NZ_CP009279_10

>10.1|6083018|37|NZ_CP009279|CRISPRCasFinder
CTACTAAGTTTTGTAAAGCATATGCATCATAGGAACG

CRISPR arrays and Neighbor proteins around NZ_CP009279_10

CRISPR arrays

The CRISPR arrays of NZ_CP009279_10

>merge|NZ_CP009279|10|6082990-6083082|CRISPRCasFinder
CTTCGTACAAAACTCACTTCGGAAGCATCTACTAAGTTTTGTAAAGCATATGCATCATAGGAACGCTTCGTACAAAACTCACTTCGAAAGCAT

>NZ_CP009279|10|10|6082990-6083082|CRISPRCasFinder
CTTCGTACAAAACTCACTTCGGAAGCAT	CTACTAAGTTTTGTAAAGCATATGCATCATAGGAACG
CTTCGTACAAAACTCACTTCGAAAGCAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042192142.1|6081267_6082071_+|polysaccharide-deacetylase-family-sporulation-protein-PdaB	unknown	unknown	gnl|CDD|200573
NZ_CP009279.1|WP_042132517.1|6083222_6083813_-|KinB-signaling-pathway-activation-protein	unknown	unknown	gnl|CDD|372908
NZ_CP009279.1|WP_042192130.1|6070529_6070709_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042192155.1|6087888_6088581_-|phosphoadenylyl-sulfate-reductase	unknown	unknown	gnl|CDD|234997
NZ_CP009279.1|WP_143759592.1|6071544_6072042_-|transcriptional-regulator	unknown	unknown	gnl|CDD|273725
NZ_CP009279.1|WP_042192153.1|6086681_6087851_-|sulfate-adenylyltransferase	unknown	unknown	gnl|CDD|235227
NZ_CP009279.1|WP_042194594.1|6072786_6073200_+|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl|CDD|368753
NZ_CP009279.1|WP_042192157.1|6089884_6090679_-|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl|CDD|234577
NZ_CP009279.1|WP_019908254.1|6090979_6091345_-|50S-ribosomal-protein-L17	unknown	unknown	gnl|CDD|235522
NZ_CP009279.1|WP_025706574.1|6088816_6089209_-|30S-ribosomal-protein-S9	unknown	unknown	gnl|CDD|178888
NZ_CP009279.1|WP_042192135.1|6072326_6072755_+|transcriptional-regulator	unknown	unknown	gnl|CDD|379262
NZ_CP009279.1|WP_042192128.1|6069207_6070530_-|phage-like-element-PBSX-protein-XkdK	unknown	unknown	gnl|CDD|377435
NZ_CP009279.1|WP_042192133.1|6070705_6071119_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042192146.1|6083942_6084614_+|hypothetical-protein	unknown	unknown	gnl|CDD|380050
NZ_CP009279.1|WP_036680631.1|6080064_6080295_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042192144.1|6082121_6082943_-|polyphosphate-kinase	unknown	unknown	gnl|CDD|274737
NZ_CP009279.1|WP_036680589.1|6089229_6089667_-|50S-ribosomal-protein-L13	unknown	unknown	gnl|CDD|181703
NZ_CP009279.1|WP_042192138.1|6080547_6081159_-|stage-II-sporulation-protein-M	unknown	unknown	gnl|CDD|224219
NZ_CP009279.1|WP_042192149.1|6084672_6085773_-|Mrp/NBP35-family-ATP-binding-protein	unknown	unknown	gnl|CDD|378455
NZ_CP009279.1|WP_042192151.1|6085862_6086603_-|N-acetylmuramoyl-L-alanine-amidase-CwlD	unknown	unknown	gnl|CDD|274337

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042192142.1|6081267_6082071_+|polysaccharide-deacetylase-family-sporulation-protein-PdaB	gnl|CDD|200573	cd10949, CE4_BsPdaB_like, Putative catalytic NodB homology domain of Bacillus subtilis putative polysaccharide deacetylase PdaB, and its bacterial homologs. The Bacillus subtilis genome contains six polysaccharide deacetylase gene homologs: pdaA, pdaB (previously known as ybaN), yheN, yjeA, yxkH and ylxY. This family is represented by the putative polysaccharide deacetylase PdaB encoded by the pdaB gene on sporulation of Bacillus subtilis. Although its biochemical properties remain to be determined, the PdaB (YbaN) protein is essential for maintaining spores after the late stage of sporulation and is highly conserved in spore-forming bacteria. The glycans of the spore cortex may be candidate PdaB substrates. Based on sequence similarity, the family members are classified as carbohydrate esterase 4 (CE4) superfamily members. However, the classical His-His-Asp zinc-binding motif of CE4 esterases is missing in this family.	2.82197e-100
NZ_CP009279.1|WP_042132517.1|6083222_6083813_-|KinB-signaling-pathway-activation-protein	gnl|CDD|372908	pfam14089, KbaA, KinB-signalling pathway activation in sporulation. This family of small proteins is found in the membrane and is necessary for kinase KinB signalling during sporulation. There is a conserved GFF sequence motif. The initiation of sporulation in Bacillus subtilis is dependent on the phosphorylation of the Spo0A transcription factor mediated by the phospho-relay and by two major kinases, KinA and KinB.	9.26659e-50
NZ_CP009279.1|WP_042192128.1|6069207_6070530_-|phage-like-element-PBSX-protein-XkdK	gnl|CDD|377435	pfam04984, Phage_sheath_1, Phage tail sheath protein subtilisin-like domain. This entry represents the second domain in a variety of phage tail sheath proteins. According to ECOD this domain has a subtilisin-like structure.	4.95017e-31
NZ_CP009279.1|WP_042192155.1|6087888_6088581_-|phosphoadenylyl-sulfate-reductase	gnl|CDD|234997	PRK02090, PRK02090, phosphoadenylyl-sulfate reductase.	2.56635e-111
NZ_CP009279.1|WP_143759592.1|6071544_6072042_-|transcriptional-regulator	gnl|CDD|273725	TIGR01637, Putative_autolysin_regulatory_protein_ArpU, phage transcriptional regulator, ArpU family. This model represents a family of phage proteins, including ArpU, called a putative autolysin regulatory protein. ArpU was described as a regulator of cellular muramidase-2 of Enterococcus hirae but appears to have been cloned from a prophage. This family appears related to the RinA family of bacteriophage transcriptional activators and to some sporulation-specific sigma factors. We propose that this is a phage transcriptional activator family. [Mobile and extrachromosomal element functions, Prophage functions, Regulatory functions, DNA interactions].	1.05782e-14
NZ_CP009279.1|WP_042192153.1|6086681_6087851_-|sulfate-adenylyltransferase	gnl|CDD|235227	PRK04149, sat, sulfate adenylyltransferase; Reviewed.	0
NZ_CP009279.1|WP_042194594.1|6072786_6073200_+|ImmA/IrrE-family-metallo-endopeptidase	gnl|CDD|368753	pfam06114, Peptidase_M78, IrrE N-terminal-like domain. This entry includes the catalytic domain of the protein ImmA, which is a metallopeptidase containing an HEXXH zinc-binding motif from peptidase family M78. ImmA is encoded on a conjugative transposon. Conjugating bacteria are able to transfer conjugative transposons that can, for example, confer resistance to antibiotics. The transposon is integrated into the chromosome, but during conjugation excises itself and then moves to the recipient bacterium and re-integrate into its chromosome. Typically a conjugative tranposon encodes only the proteins required for this activity and the proteins that regulate it. During exponential growth, the ICEBs1 transposon of Bacillus subtilis is inactivated by the immunity repressor protein ImmR, which is encoded by the transposon and represses the genes for excision and transfer. Cleavage of ImmR relaxes repression and allows transfer of the transposon. ImmA has been shown to be essential for the cleavage of ImmR. This domain is also found in in metalloprotease IrrE, a central regulator of DNA damage repair in Deinococcaceae, HTH-type transcriptional regulators RamB and PrpC.	1.84277e-16
NZ_CP009279.1|WP_019908254.1|6090979_6091345_-|50S-ribosomal-protein-L17	gnl|CDD|235522	PRK05591, rplQ, 50S ribosomal protein L17; Validated.	4.00554e-65
NZ_CP009279.1|WP_025706574.1|6088816_6089209_-|30S-ribosomal-protein-S9	gnl|CDD|178888	PRK00132, rpsI, 30S ribosomal protein S9; Reviewed.	3.0693e-87
NZ_CP009279.1|WP_042192135.1|6072326_6072755_+|transcriptional-regulator	gnl|CDD|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	4.24117e-17
NZ_CP009279.1|WP_042192149.1|6084672_6085773_-|Mrp/NBP35-family-ATP-binding-protein	gnl|CDD|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	2.28489e-125
NZ_CP009279.1|WP_042192146.1|6083942_6084614_+|hypothetical-protein	gnl|CDD|380050	pfam17898, GerD, Spore germination GerD central core domain. This is the central core domain found in GerD from a thermophilic Bacillus. GerD plays a critical role in nutrient receptor-mediated spore germination in Bacillus species. The crystal structure of GerD reveals this domain as a trimeric superhelical rope fold. Alterations in GerD structure have profound effects on spores' nutrient germination.	1.81771e-38
NZ_CP009279.1|WP_042192144.1|6082121_6082943_-|polyphosphate-kinase	gnl|CDD|274737	TIGR03709, PPK2_rel_1, polyphosphate:nucleotide phosphotransferase, PPK2 family. Members of this protein family belong to the polyphosphate kinase 2 (PPK2) family, which is not related in sequence to PPK1. While PPK1 tends to act in the biosynthesis of polyphosphate, or poly(P), members of the PPK2 family tend to use the terminal phosphate of poly(P) to regenerate ATP or GTP from the corresponding nucleoside diphosphate, or ADP from AMP as is the case with polyphosphate:AMP phosphotransferase (PAP). Members of this protein family most likely transfer the terminal phosphate between poly(P) and some nucleotide, but it is not clear which. [Central intermediary metabolism, Phosphorus compounds].	7.76091e-138
NZ_CP009279.1|WP_036680589.1|6089229_6089667_-|50S-ribosomal-protein-L13	gnl|CDD|181703	PRK09216, rplM, 50S ribosomal protein L13; Reviewed.	1.61241e-94
NZ_CP009279.1|WP_042192138.1|6080547_6081159_-|stage-II-sporulation-protein-M	gnl|CDD|224219	COG1300, SpoIIM, Uncharacterized membrane protein [Function unknown].	2.04898e-20
NZ_CP009279.1|WP_042192157.1|6089884_6090679_-|tRNA-pseudouridine(38-40)-synthase-TruA	gnl|CDD|234577	PRK00021, truA, tRNA pseudouridine(38-40) synthase TruA.	1.70359e-113
NZ_CP009279.1|WP_042192151.1|6085862_6086603_-|N-acetylmuramoyl-L-alanine-amidase-CwlD	gnl|CDD|274337	TIGR02883, spore_cwlD, N-acetylmuramoyl-L-alanine amidase CwlD. Members of this protein family are the CwlD family of N-acetylmuramoyl-L-alanine amidase. This family has been called the germination-specific N-acetylmuramoyl-L-alanine amidase. CwlD is required, along with the putative deactylase PdaA, to make muramic delta-lactam, a novel peptidoglycan constituent found only in spores. CwlD mutants show a germination defect. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Sporulation and germination].	1.73739e-101

Protein sequences

>NZ_CP009279.1|WP_042192144.1|6082121_6082943_-|polyphosphate-kinase
MDIKRYMIKDTKEIRLNKLDPDDTGVFKSKKEVEAKTEELKARLAELQDILFAQKKHSLLVILQGMDSSGKDGTVKHIFSGINPQGFIVTSFKKPSLEEEAHDFLWRVHQKTPPKGYISAFNRSHYEDVLVPRVHGGLKKDDLKRRFRYIRQFEEMLVEEGTTIIKLFLHISKEKQLKKIKERLEDPKKHWKFDASDLQEREYWDDYQEAYEDVFKESSIDKAPWYWIPANHQWYRNYLTLSIVVKTLESLDLSYPKLNTPTPDISELISPRH
>NZ_CP009279.1|WP_042192142.1|6081267_6082071_+|polysaccharide-deacetylase-family-sporulation-protein-PdaB
MNSFYVFSGKKIKRFIYIFAAVLLAAGVVYVERGNITVFSESGPSAIYSVPTEKKLIALTFDISWGEKRPEPILKVLEDKKVDKATFFLSSPWSKTHPDIVTNIKNAGFEIGSHGHKHVNYSTLSNEEIRTQISTAHTVLTELTGTEPNLIRMPNGDFDKRVLQVASDLGYKVIQWDTDSLDWKNIGVDNIVKRVTTKAHPGDIVLLHASDSCKQTHEALPLIIDELRRQGYEFVTVSELISQSNTEGKEVRDSASLSNAIEDAAGL
>NZ_CP009279.1|WP_042192138.1|6080547_6081159_-|stage-II-sporulation-protein-M
MLSFFTFIKDLKTIRKALLLSCLLFAVGAVIGWVATSSLEKLLVQQLEGLSEISGNLRDSSNPQWSFFVFIFLNNSIKGVLIIFLGALFGILPAIFLFINGAVIGYLIHLSALQGQDLFELIVKGLLPHGIIEIPAIIIACAFGLQFGGKVVASLFSSSTKKVNRGVEWSSFMRQTLTASIWTIILLFVAAIIESTITFSLLS
>NZ_CP009279.1|WP_036680631.1|6080064_6080295_-|hypothetical-protein
MLGMLFNEKECKELDYVLRKELDEMLLDLSDQRLDQNIRHAIANRYKTVFRMYARFAPQKELSKYAWGGRSSQYKH
>NZ_CP009279.1|WP_042194594.1|6072786_6073200_+|ImmA/IrrE-family-metallo-endopeptidase
MDELINNLIKKYKTNCPFELASALGIHIRFMNLGTGTKGLYYRKLRRRFIVIHNELPVEWQRFVCAHELGHDRLHKGINRFFLEESSYFSPGKLERQANVFAVKLLSTGSNPEQEESCKSYYLRIGIPPEVQFLLEE
>NZ_CP009279.1|WP_042192135.1|6072326_6072755_+|transcriptional-regulator
MKQDFGDYMKQLRETKGLTINQLAAAAGISGSQISRIENGLRGVPKPTTLRKIAEATGVPYEELMDQAGYLQEQALPSEEIVPEWATSKDKRDFRKMLEDDGELMFDGIPLDKDDKQRIKDVLTGLFWEAKQMNKRKKSNNT
>NZ_CP009279.1|WP_143759592.1|6071544_6072042_-|transcriptional-regulator
MMNLSALPELDRRRTQVAIESMLEKYRIFKTVTFEAKEASTTYSYTERFHGPTNTVTDQTAAIASYNVDIPAARRAFCSAIDSVVERLDTREQQLVRERYMKRDETYDYTIYNHVFDPPVSKDTYVKIRSKAFYKMALALTDLGLLSLNTLITAPRVKKEKISIT
>NZ_CP009279.1|WP_042192133.1|6070705_6071119_-|hypothetical-protein
MSVQQLREHITSALERYFPDVPVYVEGEKPQTAYFYPGLISATLDRQREGRYLAVYRFGIRYEKGSLLEAERMADKLSEAMAGMEQEGGSFRVARQAWEAGVEGHGPLFTTDYMVYLQSEKPDPIKMGHMIGGERLK
>NZ_CP009279.1|WP_042192130.1|6070529_6070709_-|hypothetical-protein
MSTKVSNGDRFGKEQIVNSSLFTAKEKDVLNVILQDDKSYTIEEAKQSMGLFMNKEVLN
>NZ_CP009279.1|WP_042192128.1|6069207_6070530_-|phage-like-element-PBSX-protein-XkdK
MAGGTWTTQNKVRPGVYVNVASNQGAIGKMGERGITALALALSWGEAGVIMKITPQDDVNKLLGYDLEHPTLLPVREALKRAGTLLLYRLNEGVKAAVTNNGLQVTAKYGGLRGNDLSVVIEKNIENNALFDVKTLLNGTELNKQTVGTAEELVANDYVQFQKNGAEGLKLTAGMPLIGGANGTVTNGAHSDFLSALEVLEFQTVGLVSQDSTLKALYSSWVRRLRDTEGKKVQAVLSDYATAGHEGVISVKNGVVLSDGTMIDNNNAVAWVAGATAAAAVNQSLTYQGYDDSVDADVRLSHSETTAALLRGELLFTYSGGRAVVEQDINTFTAFSPDKGKAFSKNRVLRVLDGIANDLKRIFENYYIGKVANNEDGRALFWSQCATYMNDLQDMGAIEGFNAQTDVVVVAGADSDSIVLDVAVKPVDSVEKVYMKVKVV
>NZ_CP009279.1|WP_042132517.1|6083222_6083813_-|KinB-signaling-pathway-activation-protein
MSIKKWFHLFWTTLLIGAGGAVIAGLALQFVNGKIDFKSVGDFFLYPLILLGYGMLVSVYSQLGFFAYLILNYMGNGVFPQKVWKYIQLVLSVLALLELIFLRTVVGGERNVMSDLILGIVILLAAIIVSYFKVKSTNISALIPTLFFMTAISIVEVIGVLRIGVDSATVFIVVPLIACNAFQILMLHRILKPAAG
>NZ_CP009279.1|WP_042192146.1|6083942_6084614_+|hypothetical-protein
MKWRFIGSVGLALSFVMALTACGSEQSSSSSGQGSYKETKTMVLDILKSDEGKKAVEESLSSSSSSGTSGMSMKMMPLQTTEEIKLAVKNTLTAPEYQKEIEKIMTDPKFAGDFAKAIQSQSKELHLQLIKDPTYQKSVEEIMKSPEMMTMFLNLTKTPDYRKQSMKTMQESMQTPLFRMEVLNLLKKVVQEELEPKEKKEKGSEGGDKQESSGGGSGDDSSS
>NZ_CP009279.1|WP_042192149.1|6084672_6085773_-|Mrp/NBP35-family-ATP-binding-protein
MLTKEQIQEILQPLTDSETGKSLVELQLIRDIMIKEDRISLSIICLNPEEQSRMDLEQQVRELLEAGGVSNVHIRLRDATDYERAILRGESVEDFDEPGKLKGHAAGLDDHELISESSGVNFIAVASGKGGVGKSTVTVNLAVALARKGKKVGLIDADIYGFSIPDMMGIEEGPVVEEGTIIPVERFGVKVMSMGFFIRENSPVIWRGPMLGKMLRQFFNDVGWGELDYMLLDLPPGTGDVALDVHQMLPHSKEIIVTTPHATAAFVAARAGSMALQTDHEIIGVIENMAYYECTDCGKKDYIFGRGGGARLAETLHTELLAQIPLGAPDNHISELDFSPSVYKEETPSGQLFAEIADKLIAKYEH
>NZ_CP009279.1|WP_042192151.1|6085862_6086603_-|N-acetylmuramoyl-L-alanine-amidase-CwlD
MSGRKQSKVSVWISWSSIKKSMLGVMLLAIMIGIIAYDMPTAKTLNYWSLPLSGKVIALDAGHGGADGGAVSREGLIEKDINLAVSLYLRDYLQQAGAIVVMTREGDYDLAQEGTKGYSKRKTEDLKQRVRSIEEKGADLFISVHMNSVPSNRWSGAQTFYYPNHKDNKAIAEFVQSELKTTLENTDRVAKTVNTVYLLKALKIPAVLVEVGFLSHPQESALLGNDVYQRKVATSIYRGILRYASE
>NZ_CP009279.1|WP_042192153.1|6086681_6087851_-|sulfate-adenylyltransferase
MTSIRPHGGALVNRVVEGTEREELLNLARDSKAIVLNTWTLSDLDLIAVGAFSPLTGFLNEQDYHSVVKSMRLADGTVWSIPITLAVEDDVAASLSIGDKVSLIGEDDGEIYGLLDIESIYTVDQTIEAQNVFKTTDPEHPGVSKLLARPATYVGGPITVLNRPQPEKFGEFYFDPADTRKIFAEKGWRTVVGFQTRNPVHRAHEYIQKCAMEVVDALFLNPLVGETKSDDVPANVRMKSYLALLENYYPEDRTFLGVFPAAMRYAGPREAIFHAMVRKNYGCTHFIVGRDHAGVGDYYGTYEAQEIFSNFSAEELDITPLFFEHSFFCKKCGNMASSKTCPHPSDDHMTLSGTKVRALLRDGQCPPPEFTRPEVAQILIEGMTQEVTA
>NZ_CP009279.1|WP_042192155.1|6087888_6088581_-|phosphoadenylyl-sulfate-reductase
MNLLEKEDLIRIKAEELESASPEDIIRWAVETFPNITFACSFGAEDVVLVDMLHKVSPSTDVFYLDTDYHFKETYETRDLMADKYGLEFVRVSPQLTTQEQALQYGDALWTVDPNQCCGIRKVEPLTRILSQYEAWITGIRRDQAPTRANAKKVEYDYKFGLVKFNPIADWTSEDVWNYIRENDVIYNPLHDRNYPSIGCEQCTRQVMPGEDPRAGRWSGSEKTECGLHK
>NZ_CP009279.1|WP_025706574.1|6088816_6089209_-|30S-ribosomal-protein-S9
MAQVQYYGTGRRKHSVARVRLVPGEGRIVINKREMDEYFGVETLKMIVKQPLNLTETLGNYDVIVLAHGGGISGQAGAIRHGISRALLKVDPEYRGALKKAGFLTRDPRMKERKKYGLKAARRAPQFSKR
>NZ_CP009279.1|WP_036680589.1|6089229_6089667_-|50S-ribosomal-protein-L13
MRTTYMAKPNEVERNWHIIDAEGKTLGRLASEAAALIRGKHKPQFTPHVDTGDFVIVINAEKIHLTGKKLQNKKYYRHSMHPGGLKVTNAETLLNTKPERVIEFAVHGMIPKTRQGDHMKLRLKVYAGAEHPHAAQKPEVYELRG
>NZ_CP009279.1|WP_042192157.1|6089884_6090679_-|tRNA-pseudouridine(38-40)-synthase-TruA
MRNLLMKVNYDGTNYDGFQTQPQGNTIQDRLEQAILHLTGEELKITASGRTDAGVHAYGQPFNFTTSSRIPLERWCLALNARLPQDIVVTEAREVPLTFHSRRGAKRKTYRYTINGNRFPDPFQRRWQLHHPVRLDIPAMQQGLTHILGTHDFTSFASRRSTKASHVRTIFEAHMEVDRSMCRPSSLDQGVIQTYITGSGFLQHMVRIIMGTLIHVGEGKIDADHVAEILAACDRSAAGPTAMAKGLALWSVEYDETESESFFL
>NZ_CP009279.1|WP_019908254.1|6090979_6091345_-|50S-ribosomal-protein-L17
MAYQKLGRDSSARKALFRDMVTDLFLYERIQTTEAKAKEVRSIAEKLITKAKKGDLHARRQVAAFVRRETVDGEQDAIQKLFSDIAPRYTERPGGYTRILKLGPRRGDAAPMVYLELVDRA

Crispr_ID: NZ_CP009279_11

• CRISPR_ID: NZ_CP009279_11
• CRISPR_location: 6463293-6463430
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP009279_11

Consensus_repeat	Method
AATTAGGGAAAAGCTCCCTAAAAAT	CRISPRCasFinder

spacers of NZ_CP009279_11

>11.1|6463318|26|NZ_CP009279|CRISPRCasFinder
ATTCGATATTCGCTTATAATCAACGA
>11.2|6463369|37|NZ_CP009279|CRISPRCasFinder
TAGGGTAATGCCTTGATTTCCCACCAAATCAGATGAA

CRISPR arrays and Neighbor proteins around NZ_CP009279_11

CRISPR arrays

The CRISPR arrays of NZ_CP009279_11

>merge|NZ_CP009279|11|6463293-6463430|CRISPRCasFinder
AATTAGGGAAAAGCTCCCTAAAAATATTCGATATTCGCTTATAATCAACGAAATTAGGGAAAAGCTCCCTGAAAATTAGGGTAATGCCTTGATTTCCCACCAAATCAGATGAATTTTAGGGATATTTTCCCTAATTAT

>NZ_CP009279|11|11|6463293-6463430|CRISPRCasFinder
AATTAGGGAAAAGCTCCCTAAAAAT	ATTCGATATTCGCTTATAATCAACGA
AATTAGGGAAAAGCTCCCTGAAAAT	TAGGGTAATGCCTTGATTTCCCACCAAATCAGATGAA
TTTTAGGGATATTTTCCCTAATTAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009279.1|WP_042192692.1|6471959_6472811_+|1,4-dihydroxy-6-naphthoate-synthase	unknown	unknown	gnl|CDD|270353
NZ_CP009279.1|WP_042192664.1|6455733_6456834_-|myristoyl-transferase	unknown	unknown	gnl|CDD|378117
NZ_CP009279.1|WP_042194667.1|6461605_6463078_+|alpha-amylase	unknown	unknown	gnl|CDD|236518
NZ_CP009279.1|WP_042192671.1|6459874_6461467_+|diguanylate-cyclase	unknown	unknown	gnl|CDD|379902
NZ_CP009279.1|WP_042192667.1|6457993_6458806_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223673
NZ_CP009279.1|WP_042192660.1|6452775_6454134_-|aspartate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|181078
NZ_CP009279.1|WP_042192677.1|6467023_6468256_-|multidrug-effflux-MFS-transporter	unknown	unknown	gnl|CDD|340878
NZ_CP009279.1|WP_042192673.1|6463627_6466279_-|bifunctional-lysylphosphatidylglycerol-flippase/synthetase-MprF	unknown	unknown	gnl|CDD|225451
NZ_CP009279.1|WP_042192694.1|6473104_6473926_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|369777
NZ_CP009279.1|WP_156113251.1|6470536_6470959_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP009279.1|WP_042192675.1|6466561_6466912_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP009279.1|WP_042192662.1|6454165_6455629_-|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|143404
NZ_CP009279.1|WP_042192679.1|6468410_6469031_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223477
NZ_CP009279.1|WP_042192656.1|6449402_6450794_-|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|236967
NZ_CP009279.1|WP_042192683.1|6469995_6470397_-|DoxX-family-protein	unknown	unknown	gnl|CDD|225168
NZ_CP009279.1|WP_042192689.1|6471297_6471960_+|futalosine-hydrolase	unknown	unknown	gnl|CDD|350166
NZ_CP009279.1|WP_042192681.1|6469027_6469978_-|ring-cleaving-dioxygenase	unknown	unknown	gnl|CDD|319935
NZ_CP009279.1|WP_042192658.1|6451112_6452801_+|PucR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|377939
NZ_CP009279.1|WP_081951232.1|6457076_6457994_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223673
NZ_CP009279.1|WP_042192669.1|6458808_6459591_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224041

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP009279.1|WP_042192692.1|6471959_6472811_+|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.	2.34327e-130
NZ_CP009279.1|WP_042192664.1|6455733_6456834_-|myristoyl-transferase	gnl|CDD|378117	pfam09084, NMT1, NMT1/THI5 like. This family contains the NMT1 and THI5 proteins. These proteins are proposed to be required for the biosynthesis of the pyrimidine moiety of thiamine. They are regulated by thiamine. The protein adopts a fold related to the periplasmic binding protein (PBP) family. Both pyridoxal-5'-phosphate (PLP) and an iron atom are bound to the protein suggesting numerous residues of the active site necessary for HMP-P biosynthesis. The yeast protein is a dimer and, although exceptionally using PLP as a substrate, has notable similarities with enzymes dependent on this molecule as a cofactor.	1.23678e-46
NZ_CP009279.1|WP_042194667.1|6461605_6463078_+|alpha-amylase	gnl|CDD|236518	PRK09441, PRK09441, cytoplasmic alpha-amylase; Reviewed.	0
NZ_CP009279.1|WP_042192671.1|6459874_6461467_+|diguanylate-cyclase	gnl|CDD|379902	pfam16927, HisKA_7TM, N-terminal 7TM region of histidine kinase. HisKA_7TM is an N-terminal region consisting of seven transmembrane domains found in Archaea and some bacteria. It is always found associated with histidine kinase.	4.06751e-65
NZ_CP009279.1|WP_042192667.1|6457993_6458806_-|ABC-transporter-permease	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	1.45728e-47
NZ_CP009279.1|WP_042192660.1|6452775_6454134_-|aspartate-aminotransferase-family-protein	gnl|CDD|181078	PRK07678, PRK07678, aminotransferase; Validated.	0
NZ_CP009279.1|WP_042192677.1|6467023_6468256_-|multidrug-effflux-MFS-transporter	gnl|CDD|340878	cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging 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.	9.5149e-99
NZ_CP009279.1|WP_042192673.1|6463627_6466279_-|bifunctional-lysylphosphatidylglycerol-flippase/synthetase-MprF	gnl|CDD|225451	COG2898, COG2898, Uncharacterized conserved protein [Function unknown].	4.00942e-125
NZ_CP009279.1|WP_042192694.1|6473104_6473926_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	1.72258e-22
NZ_CP009279.1|WP_156113251.1|6470536_6470959_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.2657e-23
NZ_CP009279.1|WP_042192662.1|6454165_6455629_-|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	gnl|CDD|143404	cd07085, ALDH_F6_MMSDH, Methylmalonate semialdehyde dehydrogenase and ALDH family members 6A1 and 6B2. Methylmalonate semialdehyde dehydrogenase (MMSDH, EC=1.2.1.27) [acylating] from Bacillus subtilis is involved in valine metabolism and catalyses the NAD+- and CoA-dependent oxidation of methylmalonate semialdehyde into propionyl-CoA. Mitochondrial human MMSDH ALDH6A1 and Arabidopsis MMSDH ALDH6B2 are also present in this CD.	0
NZ_CP009279.1|WP_042192679.1|6468410_6469031_-|alpha/beta-hydrolase	gnl|CDD|223477	COG0400, COG0400, Predicted esterase [General function prediction only].	2.73487e-66
NZ_CP009279.1|WP_042192656.1|6449402_6450794_-|NAD(P)-dependent-oxidoreductase	gnl|CDD|236967	PRK11749, PRK11749, dihydropyrimidine dehydrogenase subunit A; Provisional.	0
NZ_CP009279.1|WP_042192683.1|6469995_6470397_-|DoxX-family-protein	gnl|CDD|225168	COG2259, COG2259, Predicted membrane protein [Function unknown].	3.33305e-17
NZ_CP009279.1|WP_042192689.1|6471297_6471960_+|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.	3.68549e-73
NZ_CP009279.1|WP_042192681.1|6469027_6469978_-|ring-cleaving-dioxygenase	gnl|CDD|319935	cd08347, PcpA_C_like, C-terminal domain of Sphingobium chlorophenolicum 2,6-dichloro-p-hydroquinone 1,2-dioxygenase (PcpA), and similar proteins. The C-terminal domain of Sphingobium chlorophenolicum (formerly Sphingomonas chlorophenolica) 2,6-dichloro-p-hydroquinone 1,2-dioxygenase (PcpA), and similar proteins. PcpA is a key enzyme in the pentachlorophenol (PCP) degradation pathway, catalyzing the conversion of 2,6-dichloro-p-hydroquinone to 2-chloromaleylacetate. This domain belongs to a conserved domain superfamily that is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases.	3.31684e-57
NZ_CP009279.1|WP_042192658.1|6451112_6452801_+|PucR-family-transcriptional-regulator	gnl|CDD|377939	pfam07905, PucR, Purine catabolism regulatory protein-like family. The bacterial proteins found in this family are similar to the purine catabolism regulatory protein expressed by Bacillus subtilis (PucR). PucR is thought to be a transcriptional activator involved in the induction of the purine degradation pathway, and may contain a LysR-like DNA-binding domain. It is similar to LysR-type regulators in that it represses its own expression. The other members of this family are also annotated as being putative regulatory proteins.	8.53091e-38
NZ_CP009279.1|WP_081951232.1|6457076_6457994_-|ABC-transporter-permease	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	1.36594e-49
NZ_CP009279.1|WP_042192669.1|6458808_6459591_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224041	COG1116, TauB, ABC-type nitrate/sulfonate/bicarbonate transport system, ATPase component [Inorganic ion transport and metabolism].	3.2091e-112

Protein sequences

>NZ_CP009279.1|WP_042194667.1|6461605_6463078_+|alpha-amylase
MMRNHTMMQFFEWHVAADGKHWDRLKETASALKAVGIDSVWVPPVTKAVSADDTGYGVYDLYDLGEYDQKGTVRTKYGTKQALIEAISECQKNGIAVYVDLVMNHKAGADEKEVFQVIEVDPNDRMKEISKPFEIEGWTKFTFPGRGDEHSSFKWNHNHFNGTDFDAKSGRTGVFRIAGENKTWNQNVDDEFGNYDYLMFANIDYSHPEVKKEMIQWGKWLVDTLHCSGFRLDAIKHINHEFVKQFAVEMFNKCEKDFYIVGEFWNSDLESCRQFLNTVDYKIDLFDVSLHYKLHSASLGGRNFDLTKILDDTLVQTHPTNAVTFVDNHDSQPHEALESWVDDWFKQSAYALILLRRDGYPVVFYGDYYGIEGPTPVAGKKEAIDPLLYTRYHKAYGEQKDYFDHPNTIGWTRLGVKDIERSGCAVVISNGENGQKRMFVGEQRAGEAWVDFTHNHKATITIEKDGWATFPVNGGSVSVWALPDEKADEK
>NZ_CP009279.1|WP_042192671.1|6459874_6461467_+|diguanylate-cyclase
MGSVISNYIVIVAISGVLSVLLALFAYYKKTDFLGIRAFVISSFTSAIYTFGFALELSGKTLEEMSFWIKVEYLGMPFIAPASLIMVMHFVGLESLIKKGMRAALYIIPFITTLMVWTNDYHHLFYKSIYLRDNTPSPLVDVVMGPWYIVHGSFTFGCLLAAICLMLWQWNRMKRVYRRQIVTILIGLSLPTLGSFLYLMGLTPYGMDPVPIIMSITSTLYIWAILSRGMLTAAPIARENLFESMRDGVLVTDRSDMLVDYNRAAADMIEGLNSSAIGKPLAQLFLNAGKDALSYVMDTEPLQREEREVAWIKGDEICYYQIRSSPVQKQGGYLAGQMIMLIDVTERILLQDKLRQLATMDSLTGIYNRTYFLELSRGLLVQAASNRSSLSIILLDVDFFKSINDRFGHQYGDQALQHIVEVCNRHIREGDIFGRYGGEEFVICLPDTSLKQAAQLCETIRADIEQSVLYTLIGSINVTASFGVVEALSPKATLEELLSEADHALYSSKRNGRNAVHLSQRSEITLFKPI
>NZ_CP009279.1|WP_042192669.1|6458808_6459591_-|ABC-transporter-ATP-binding-protein
MSLLATNIPEIQLENVEMRYRAEAAEVLALHQVSLDIAKGEFVSLLGPSGCGKTTLLRLMADLIAPTGGNIVVAGKSAKEARLAQKYGIVFQSPVLYDWRKVKHNITLPLELMGVKKSIREERALELLDLVGLQSFADKYSWQLSGGMQQRVAIARALSMEPEILLMDEPFSALDEFTRERLNEELLSVWSKVQNTIVFVTHSIPESIFLSDRVFVLSPHPGRLSAVVEIPLPRPRTAEMRNSPEFFELIASIRDSFEGV
>NZ_CP009279.1|WP_042192667.1|6457993_6458806_-|ABC-transporter-permease
MKGGSIFVRGRLLPLFVWIFGLLLVWEGTSWMLLHVVETPLAQSKLPYVHEVLSTLWKYSGTLLKEGAATFGNAGVGFLIGAVAGASLAVLMSLSKTIERLTFPYAIASQMIPILGLAPIIYGIVRDEQTSRIIISGYITFFPVALNMLRGLRSVDPSALELMHSYAAKPWAVYWKLRFPAALPGLFGGLKIAAPLAVTGAILVELMGAQHGIGVIMLRNLYYGSSHTYMFWSTVIVGALLGIVSYWLISLIERLVAPWQPEFRPKGGSR
>NZ_CP009279.1|WP_081951232.1|6457076_6457994_-|ABC-transporter-permease
METNSVREASFMGSSGKEMAQPALTATQKNAVAVPKPAEATASRGGSRMLKRIFSAGVLLPVLAGVLFLGLWEFEFFHKIFDLKKYQLPLPTAIATTMRDNFSMLLSYTGYTLTEAVLGMLVGSAIGFLIALAATAWPRWGSGSLTLVAALNAVPIVALAPIMNLWFGDGIGSRIAIVTATTMAAMAINAYKGMAAIDPLALDLMHSYAAGKPAVFRYLRIRNSLPYVFTALKINATASMIGAIVGEFFFSSKGLGYLLSNSIKVAKMPLGWSCIVLAAIAGVLFYLVVERLEKVFIKWHPSQRK
>NZ_CP009279.1|WP_042192664.1|6455733_6456834_-|myristoyl-transferase
MNGKKRKFRGGLLAIVMMLSVSLMAGCGGNNNNSAAEATTAPEASTAPEASATAEPAADPVTVKLQLKWVPQAQFAGYFVAQDKGYYKEEGLNVEILPGGPDIVPEQQVAGGSADIGVGWVASLLPSLEEGMPLVQIAQIYQKSGLVLVSKKSAGINSAADLKGKKVGNWMGGNEFELLALFDKYKFDPNKDLSFTKQGFTMDQFLGDQIDAASAMTYNEYQVVLESGVKAEDLNVIDMNTEGVAMLEDNLFANKEWLAENKETAAKFVRASLKGWKAAIADPAAAVDSVMKQAEDGSTTKEHQLTMMTEVAKLILPEGFDSAKMGYTDAAAFQQTADISQKFGVIKEPAKVDEAYTNEIVEMAAK
>NZ_CP009279.1|WP_042192662.1|6454165_6455629_-|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase
MSLLVTQAERVKNYVNGAWVESSSGRDEEVYNPATGKVIAYVPISSKEELSAAVEAAAVAFQAWKRVAVPRRARYFFQYQQLLVKHWHELALLITLENGKSLEEAQGEVQRGIECVEFAAGIPTLMMGSQLPDIATGIESGMYRYPLGVIGGIAPFNFPMMVPCWMFPLAIACGNTFVLKPSERTPLLVNRLAELFAEAGFPPGVLNVVHGAHEVVNGLLEHDEVKAISFVGSQPVAEYVYKAGTAQGKRVQALAGAKNHSIVLPDAELDNAVKNIIAAAFGSAGERCMACSVVVVHEDIADELVSRLAAAADELKIGNGADDGVFLGPVIRQSNKERTLYYIETGEAEQAKLVRDGRKDAAVGGVGYFIGPTIFDHVQPGMTLWKDEIFAPVLSVIRVKSLSEAIAVTNQSPFANGACIYTDSAKAIREFREEIDAGMLGVNLGVPAPMAFFPFSGYKKSFYGDLHANGRDGVEFYTRKKMITARY
>NZ_CP009279.1|WP_042192660.1|6452775_6454134_-|aspartate-aminotransferase-family-protein
MQSLGNDSELAVSKDRKYLWHSITPYSEKNPPMIAASASGSWITDIQGNRFLDGMSGLWCVNVGYGRKELAEAAYNQLLTLPYFPLTQSHLPAIALAEKLNEWLGDEYVIFFSNSGSEANEAAFKMARQYQQQIGQHYRHKFIARYRGYHGSSLGALSATGQAQRKYKYEPLAGGFLHVAPPDSYRRPAGMTVEEFNLQCAQSIEDMIIWEGVETVAAVIMEPVITGGGVIVPHQVYLDRVQEICRKHGVLLIMDEVICGFGRSGRKFGHHNFNVKPDIVTMAKGLTSAYLPLSATAVRKDIYKVFKDNSDDYGYFRHVNTFGGNPASCALALRNLEIIEQEKLVERADLLGKRINTEFTELLDHKLVGDVRSFGLVTGIELVEDKVSKKPVDLSIVKGIIAECKSKGLIIGKNGDTVAGFNNVLTLAPPLSSTDEDIEFIIDTFKSVLNGE
>NZ_CP009279.1|WP_042192658.1|6451112_6452801_+|PucR-family-transcriptional-regulator
MDWELVLTIRDALKRPLFAEAEVIGGESGLSRAIRWVHVLESANFETLIHGEEMILTTGIGASVDLPSSLEFMQNLIDKNAACLCIELGTYFSTIPQEMIDLADRHDFPLIIFTRTVRFVDITLDLHSIIINRHHRMLQELESISREFHRLTLTSQGTVKVLQLLCKSTRTQIVYMQLQGKPLFFPALPPDEQTPLLNFFTTFGDEMEGIQPDIAPYTREYGQKTIAIKPVGALDQTWAYILMVCNHKPQEFDCLLLDSASLSIAQELLRTRYMEERKLFSENLWVDELINGRIEDDNRLKGLIGSNFNMVNELPYRVCLIEIKNPRDVKWNSSENEWESITFHLSLILRSIFEKYSLRPLITLKNNRLTVIALDIQSKMPGKMRLQQALEALQNIRSDEKLKDLQLVIGVSKSHKRLKQAYSGYQEALQALSLYSCYQKSLLFYEELGVFQLLLSLNDGKTLQNFIRSYLGPLIDHDQTKGSELLLTLRVYLDHDGSKQIAAQNLFIVRQSLYYRLDKITELLGEDFMQPENRISIQVALRAYQFLYPDKITLPIPRSAQI
>NZ_CP009279.1|WP_042192656.1|6449402_6450794_-|NAD(P)-dependent-oxidoreductase
MEHSSPLTAFTPDMFRRNFAEAEPPLTHKGAMDESNRCLYCYDAPCIKACPTSINIPSFIKRIATDNMKGSAQTIMDSNPVGASCARVCPTDELCEGACVLNDASAPIQIGLLQRYATDWAMNSGVQLFKAGTPNGKKVAVIGGGPAGLSAARELAREGFAVVVYEAKALAGGLDTHGIVSFRLPQSVSLWEVEQVEKLGVEIRTGVKVGVDVSVDELKSNYDAIVLAAGMGYVPPIGIEGEKLAGVYDAIALVESTKTGIPLLELMGQRVAVIGAGNTAIDAATCSVRLGASNVKMVYRRTREEMTAYEFEYEFAKQEGVEFNWLTLPKRIVGDEFGNVTGLECAQMKLTEELGKDGRPVPMPIEGSEFLIPVDAVVIAIGQKRRLDLIDSLGLVHDRGVVKVDEATCQTSDPQIYAAGDIIFGSGKGEAMVVSAAQQGKDAAHAIVKQFLGQQEVVVRSAG
>NZ_CP009279.1|WP_042192673.1|6463627_6466279_-|bifunctional-lysylphosphatidylglycerol-flippase/synthetase-MprF
MQSKQQTLERFKIVRLFLSIYRIRAVRALFPVAIIALVYWEGQHELKQVHLGLIMRELRRVPTSAVLQMIGFALLAVAVMSAYDYLIRAHFRLKVGLWDTFRYAWIANTFNNLIGFAGLAGVGLRTLMYKKSGVSTSVLTPAIVFLSPLMITGLSLLSWANIFGLLPATALLEEHHWLVFAVWGMALYLPFFVFVQRSALYAKWINRGQGRTPWLTVVASVGASFLEWSFAGVTFWTISSHLLHEVHFPVIFGIFTIAAIAGILSMAPGGIGAFDLIALLGLTQLGFKSDQAMAVLVIFRLFYYLIPWLIGLVLAALEFGLQGKKGQDRSAPGFEPALNIWQRIWGWPGQYTFLSDLGVWALGKLVLASGLILLLSTATPGLLYRLKITEEILSFSIMQLSHHLSVLIGFMLILLSRGITLRVRSAYIWTSILLFSGSVFAVAKGFDYEEALFLLLVALILWISRSRFYRISAPVSRQSTIWWLALTSVIALSYYLLGSHVHRGFLKHLPPGVEPEWLQRHSHVAFTAVGGLAFSWIILTLLITLRPHRKPEELFGNFDMARLKNFLGEVQGNALTHMLFLGDKSFFWAQEGKVLLAFARVRDKLVVLGDPLGERSLMNEAISEFRQAADKYGLVVVFYQATPDFLSIYHEQGYRFFKLGEEALVTLDTFTLSGKKNSDLRSVCNRFEREGYAFEVVEAPHAEELLRELRSVSNEWLNGRTEKGYSLGWFNEAYLQLAPIVLLRNAQGTILAFASIANGYDQGMTLSIDLMRHRKNVPNGTMDYLFVRLLEWAKSKGYHRFNLGNAPLSSVGENAGALKEEKLAHLVFKRGGHWYGFVGLRRYKEKFSPEWEPRYLAYPASIALPILTLDLVRLVSRHPRAEE
>NZ_CP009279.1|WP_042192675.1|6466561_6466912_-|hypothetical-protein
MSISAVSGSTSYTTSTSSTTDTSTLEKQKAKLEAELDKINASSDDDKTKETKTKQIEQQIKTIEAQISQKSQSSASSASSVVEAPAKPANNTLAAASPQEIATATTDSKGRFDIRV
>NZ_CP009279.1|WP_042192677.1|6467023_6468256_-|multidrug-effflux-MFS-transporter
MIGIQNGNKLAADGPSRKQRLQLAVILGSITTIGPLSIDMYLPALPTLVADFGTTAALVQLSLTFFLLGLASGQLVAGPLSDVYGRRGPLLIGMFIYAVSSVLCAFSPSIGLLIVLRFIQGLAGSVGVVVSRAAVRDLYSGSELTKFFSLLMIVNGLGPILAPVIGGQLLRVTTWQGIFLVLFAAGIIFCLTILLRLPETLPKERRSKSGLKGTLLTFRVLLGNRKFMGYALSQGFVTASMFAYISGSSFVLQNIFAVTPQVYSLIFAVNGIGIIITGQIAGRLAGKVSETKLLLSGLLLCTMGGILLLLTVLVGGGLIPILICLFAVVSSVGIVGATSFSLAMQDQGETAGSASALIGLIPLLLGSCVAPLVGLGGVESALPMAIVMACTGILSILSYVLLVRRGKASS
>NZ_CP009279.1|WP_042192679.1|6468410_6469031_-|alpha/beta-hydrolase
MIHVFHKGKDVTKPTLVLFHGTGGNEQDLLPLAGLLSPDSSVLGIRGNVLENGMPRFFRRLAEGVFDEADLIFRTHEIKQFLDEAAAQYGFDANNLVAVGYSNGANIAGSLLFHYKDVFRAAILLHPMVPLRNITLPSLEGVSIFIGAGTNDPLIASSETEDLDIILQKAGAEVTTHWGNQGHRLSVAEAEAARDWLQMRSTSTNA
>NZ_CP009279.1|WP_042192681.1|6469027_6469978_-|ring-cleaving-dioxygenase
MTLQTAGIHHITAFVGDAQRNVDFYAGILGLRLVKKTINFDAPEVYHLYFGNEVGAPGTIITFFPSPTGRKGRIGSGQVGVTTYAVPVGSLIFWEQRLAAYQIPVTLKHRISESYLSFADYDGLRIELVEREEGPLSKWSFGGVPTGHAIKGFGGAVLYSNNPSQTAETLVHTMGMKHIADGDGYSRYRTTGDLGNIIDLKTTPVPQGAGGTGTVHHIAWRAQDDAEQQEWGLQVQNHGHHPTPVQDRQYFNAIYFRERGGILFEIATDPPGFARDEAVDALGEKLMLPSWYEPHRAAIEENLSPFQIREIEVKQG
>NZ_CP009279.1|WP_042192683.1|6469995_6470397_-|DoxX-family-protein
MISVGILLMRLVIGIAFIGHGAQKLFGWFGGYGPKGTGGWMESIGIKPGVTMAVLAGLMELVGGFMFAAGLLTPVAAVLIVATMLGAIIKVHAPNGFWSTSNGIEFPLTVLVVAAGIALTGPGSISLDALIFN
>NZ_CP009279.1|WP_156113251.1|6470536_6470959_-|MarR-family-transcriptional-regulator
MDQASSLKLFVVLSKAYRSLMDQAVKDMKSYGLASAEFMVLEVLYHRTRIPLQQIGEKILVTSGSITYNIDKLEKKGLLKRVPCSEDRRVTYAEITDAGRALFDKIFPRHVASIHDLMRGLDKDEKGQAIELLKKLGKGV
>NZ_CP009279.1|WP_042192689.1|6471297_6471960_+|futalosine-hydrolase
MVEEQAGARRVLIVTAVAAERDAVLRGLQGSDRFHVIAAGAGTAAAAAGTAAALAAGSYGCVISAGIGGGFPGVAPLGSLVVASEMIAADLGAETPEGFRSAAELGFGSVSVPADHGTVQAVSAALAAAGLTVSTGTVLTVSTATGTAETAAALIARHPGAVAEAMEGHGVAVAAEALGLPVLELRAISNPVGPRDRAAWKIGDAMEALTAAAAILLEVL
>NZ_CP009279.1|WP_042192692.1|6471959_6472811_+|1,4-dihydroxy-6-naphthoate-synthase
MTTELNIAFSPCPNDTFVFHAWAHGLVPNAPQLNVTYADIDITNTLAANGEGPEVLKISYAALPWVLERYKLLPCGGALGRGCGPLLLTASGPTAIKRPEKLAGRRIAVPSERSTAYLLFRLWAAQHITGGIGEIVVMPFDEIMPAVRDGHIDAGLVIHEARFTYASYGLNMLTDLGSWWESDTGLPIPLGAIIARRDLDADAITGWIRSSLQYAWDHPTDSRDYVLSHAQELAPEVAKSHIDLYVNDFSMNLGDDGYAAITSLLNRAAAEGLVPAIDPALLR
>NZ_CP009279.1|WP_042192694.1|6473104_6473926_+|class-I-SAM-dependent-methyltransferase
MIPENNSKQNIDRFLGFQEDYDRYRPEAPGMIIKLLTDYLGSTPSVVADIGCGTGLSTFLWKDVADNVIGIEPNPDMLGKAIDKLSRIEDPQSITFVQGYSNQLPLAVDSVDIVTCSQSFHWMDPESTLREISRVLRTGGVFAAYDCDWPLPLQQKVEERYNQLISKSEELLASLLPDAERAHKWDKEGHLSRIQASGAFSFAREIVFHNLESCDAQRYVGLALSQGGIRTVLKQDATLLNQDIADFSAAVEDHFQGRTLEVLISYRMRIGIK

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP009279.1	6083060-6083088	2	0.931

1. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to position: 6083060-6083088, mismatch: 2, identity: 0.931

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
aagcgtatgctttcgaagtgagttttgta	Protospacer
***. ************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP009279_11	11.1|6463318|26|NZ_CP009279|CRISPRCasFinder	6463318-6463343	26	NZ_CP042620	Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-5, complete sequence	88782-88807	4	0.846
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP026134	Klebsiella pneumoniae strain F5 plasmid pF5_2, complete sequence	81265-81293	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP022128	Klebsiella pneumoniae strain DHQP1605752_NV plasmid p1605752FIB_2, complete sequence	35821-35849	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP044030	Klebsiella pneumoniae strain RJY9645 plasmid pY9645-105, complete sequence	76019-76047	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP036373	Klebsiella pneumoniae strain WCHKP020037 plasmid p1_020037, complete sequence	412-440	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP008931	Klebsiella pneumoniae strain PMK1 plasmid pPMK1-B, complete sequence	80063-80091	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP050365	Klebsiella pneumoniae strain 47733 plasmid p47733_IncFIB, complete sequence	63938-63966	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP030268	Klebsiella pneumoniae subsp. pneumoniae strain SC-7 plasmid pSC7-IncFIB-110K, complete sequence	68850-68878	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP026146	Klebsiella pneumoniae strain F132 plasmid pF132_1, complete sequence	92168-92196	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP026150	Klebsiella pneumoniae strain F138 plasmid pF138_1, complete sequence	75228-75256	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP045677	Klebsiella pneumoniae strain WSD411 plasmid pWSD411_4, complete sequence	1579-1607	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP026138	Klebsiella pneumoniae strain F77 plasmid pF77_2, complete sequence	51315-51343	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052264	Klebsiella pneumoniae strain E16KP0288 plasmid pE16K0288-2, complete sequence	319-347	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP028544	Klebsiella pneumoniae subsp. pneumoniae strain SCKP020143 plasmid p2_020143, complete sequence	1558-1586	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP023984	Klebsiella variicola strain X39 plasmid pX39-7, complete sequence	78955-78983	7	0.759
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP028550	Klebsiella variicola strain WCHKP19 plasmid p2_020019, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_MF133442	Klebsiella pneumoniae strain 11219 plasmid p11219-CTXM, complete sequence	1699-1727	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP012427	Klebsiella pneumoniae strain KP5 plasmid pSg1-1, complete sequence	60837-60865	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP017387	Klebsiella pneumoniae strain KP36 plasmid 2, complete sequence	224037-224065	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP044034	Klebsiella pneumoniae strain FDAARGOS_631 plasmid unnamed2, complete sequence	3079-3107	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052409	Klebsiella pneumoniae strain C17KP0008 plasmid pC17KP0008-2, complete sequence	1609-1637	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052311	Klebsiella pneumoniae strain E16KP0102 plasmid pE16KP0102-2, complete sequence	76435-76463	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP041929	Klebsiella pneumoniae strain 18-2374 plasmid pSECR18-2374B, complete sequence	7944-7972	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP025467	Klebsiella pneumoniae strain JS187 plasmid p187-1, complete sequence	135722-135750	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052220	Klebsiella pneumoniae strain E17KP0053 plasmid pE17KP0053-3, complete sequence	49338-49366	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052416	Klebsiella pneumoniae strain C16KP0189 plasmid pC16KP0189-2, complete sequence	1588-1616	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP024877	Klebsiella pneumoniae strain NH25 plasmid pNH25.3, complete sequence	60232-60260	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP021962	Klebsiella pneumoniae strain AR_0139 plasmid tig00000008, complete sequence	1787-1815	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP012570	Klebsiella pneumoniae strain UCLAOXA232KP plasmid pUCLAOXA232-4.X, complete sequence	1699-1727	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP031791	Klebsiella pneumoniae strain KSB1_1I-sc-2280289 plasmid unnamed2, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052552	Klebsiella pneumoniae strain A17KP0038 plasmid pA17KP0038-1, complete sequence	1609-1637	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP031803	Klebsiella pneumoniae strain MSB1_8A-sc-2280397 plasmid unnamed3, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP036194	Klebsiella pneumoniae strain BA34918 plasmid pIncFIB, complete sequence	41744-41772	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP040026	Klebsiella pneumoniae strain KPC160132 plasmid pIncFI-L132, complete sequence	20070-20098	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP028997	Klebsiella pneumoniae strain AR_0079 plasmid unnamed4, complete sequence	91278-91306	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP027045	Klebsiella pneumoniae strain 1_GR_13 plasmid IncFIB, complete sequence	27863-27891	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052281	Klebsiella pneumoniae strain E16KP0224 plasmid pE16KP0224-1, complete sequence	83516-83544	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP012565	Klebsiella pneumoniae strain UCLAOXA232KP plasmid pUCLAOXA232-4, complete sequence	1699-1727	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP035909	Klebsiella pneumoniae strain BA4656 plasmid unnamed2, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052423	Klebsiella pneumoniae strain C16KP0164 plasmid pC16KP0164-1, complete sequence	114782-114810	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP024460	Klebsiella pneumoniae strain QS17-0161 plasmid pMRSN480738_112.7, complete sequence	20857-20885	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP021714	Klebsiella pneumoniae strain AR_0129 plasmid tig00000001, complete sequence	83744-83772	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP026165	Klebsiella pneumoniae strain F81 plasmid pF81_1, complete sequence	35088-35116	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP015755	Klebsiella pneumoniae strain W14 plasmid unnamed2, complete sequence	103210-103238	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP016924	Klebsiella pneumoniae isolate 23 plasmid pIncFIB_DHQP1400954, complete sequence	61766-61794	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP032187	Klebsiella pneumoniae strain AR_0075 plasmid unnamed2, complete sequence	32683-32711	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052390	Klebsiella pneumoniae strain C17KP0052 plasmid pC17KP0052-2, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP040597	Klebsiella pneumoniae subsp. pneumoniae strain KpvST15_NDM plasmid unnamed3, complete sequence	2515-2543	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052352	Klebsiella pneumoniae strain D16KP0146 plasmid pD17KP0032-1, complete sequence	127652-127680	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NC_016838	Klebsiella pneumoniae subsp. pneumoniae HS11286 plasmid pKPHS1, complete sequence	1899-1927	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP034055	Klebsiella pneumoniae strain KP_NORM_BLD_2015_112126 plasmid unnamed2, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052393	Klebsiella pneumoniae strain C17KP0040 plasmid pC17KP0040-1, complete sequence	73427-73455	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP044370	Klebsiella pneumoniae strain 2018C01-046 plasmid p2018C01-046-2, complete sequence	38530-38558	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP034047	Klebsiella pneumoniae strain KP_NORM_BLD_2014_104014 plasmid unnamed2, complete sequence	1579-1607	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP016161	Klebsiella pneumoniae strain TH1 isolate TH1 plasmid unnamed2, complete sequence	6552-6580	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP050276	Klebsiella pneumoniae strain 10553 plasmid unnamed1, complete sequence	26719-26747	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP052470	Klebsiella pneumoniae strain C16KP0053 plasmid pC16KP0053-2, complete sequence	1588-1616	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP044046	Klebsiella pneumoniae strain FDAARGOS_629 plasmid unnamed4, complete sequence	58998-59026	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP050287	Klebsiella pneumoniae strain 9630 plasmid unnamed2, complete sequence	113909-113937	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_CP032225	Klebsiella pneumoniae strain AR_0046 plasmid unnamed3, complete sequence	25702-25730	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	NZ_KY354306	Klebsiella pneumoniae strain 301 plasmid pKP301b, complete sequence	51603-51631	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	LR134218	Klebsiella aerogenes strain NCTC10317 genome assembly, plasmid: 2	36672-36700	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	MK422451	Klebsiella phage ST13-OXA48phi12.3, complete genome	70224-70252	8	0.724
NZ_CP009279_2	2.1|1080526|29|NZ_CP009279|CRISPRCasFinder	1080526-1080554	29	CP058330	Klebsiella phage vB_Kpn_1825-KPC53 chromosome phage_vB_Kpn_1825-KPC53, complete sequence	54486-54514	8	0.724
NZ_CP009279_7	7.1|5657205|34|NZ_CP009279|CRISPRCasFinder	5657205-5657238	34	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	1149456-1149489	10	0.706
NZ_CP009279_10	10.1|6083018|37|NZ_CP009279|CRISPRCasFinder	6083018-6083054	37	AP019525	Tenacibaculum phage PTm5 DNA, complete genome	6848-6884	10	0.73
NZ_CP009279_10	10.1|6083018|37|NZ_CP009279|CRISPRCasFinder	6083018-6083054	37	AP019524	Tenacibaculum phage PTm1 DNA, complete genome	6877-6913	10	0.73

1. spacer 11.1|6463318|26|NZ_CP009279|CRISPRCasFinder matches to NZ_CP042620 (Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-5, complete sequence) position: , mismatch: 4, identity: 0.846

attcgatattcgcttataatcaacga	CRISPR spacer
cttcaatattcgcttatagtcaacgt	Protospacer
 ***.*************.****** 

2. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP026134 (Klebsiella pneumoniae strain F5 plasmid pF5_2, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

3. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP022128 (Klebsiella pneumoniae strain DHQP1605752_NV plasmid p1605752FIB_2, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

4. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP044030 (Klebsiella pneumoniae strain RJY9645 plasmid pY9645-105, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

5. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP036373 (Klebsiella pneumoniae strain WCHKP020037 plasmid p1_020037, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

6. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP008931 (Klebsiella pneumoniae strain PMK1 plasmid pPMK1-B, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

7. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP050365 (Klebsiella pneumoniae strain 47733 plasmid p47733_IncFIB, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

8. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP030268 (Klebsiella pneumoniae subsp. pneumoniae strain SC-7 plasmid pSC7-IncFIB-110K, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

9. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP026146 (Klebsiella pneumoniae strain F132 plasmid pF132_1, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

10. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP026150 (Klebsiella pneumoniae strain F138 plasmid pF138_1, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

11. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP045677 (Klebsiella pneumoniae strain WSD411 plasmid pWSD411_4, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

12. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP026138 (Klebsiella pneumoniae strain F77 plasmid pF77_2, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

13. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052264 (Klebsiella pneumoniae strain E16KP0288 plasmid pE16K0288-2, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

14. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP028544 (Klebsiella pneumoniae subsp. pneumoniae strain SCKP020143 plasmid p2_020143, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

15. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP023984 (Klebsiella variicola strain X39 plasmid pX39-7, complete sequence) position: , mismatch: 7, identity: 0.759

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccca	Protospacer
. ****.********* ********. .*

16. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP028550 (Klebsiella variicola strain WCHKP19 plasmid p2_020019, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

17. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_MF133442 (Klebsiella pneumoniae strain 11219 plasmid p11219-CTXM, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

18. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP012427 (Klebsiella pneumoniae strain KP5 plasmid pSg1-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

19. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP017387 (Klebsiella pneumoniae strain KP36 plasmid 2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

20. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP044034 (Klebsiella pneumoniae strain FDAARGOS_631 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

21. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052409 (Klebsiella pneumoniae strain C17KP0008 plasmid pC17KP0008-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

22. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052311 (Klebsiella pneumoniae strain E16KP0102 plasmid pE16KP0102-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

23. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP041929 (Klebsiella pneumoniae strain 18-2374 plasmid pSECR18-2374B, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

24. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP025467 (Klebsiella pneumoniae strain JS187 plasmid p187-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

25. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052220 (Klebsiella pneumoniae strain E17KP0053 plasmid pE17KP0053-3, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccct	Protospacer
. ****.********* ********. . 

26. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052416 (Klebsiella pneumoniae strain C16KP0189 plasmid pC16KP0189-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

27. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP024877 (Klebsiella pneumoniae strain NH25 plasmid pNH25.3, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

28. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP021962 (Klebsiella pneumoniae strain AR_0139 plasmid tig00000008, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

29. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP012570 (Klebsiella pneumoniae strain UCLAOXA232KP plasmid pUCLAOXA232-4.X, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

30. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP031791 (Klebsiella pneumoniae strain KSB1_1I-sc-2280289 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

31. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052552 (Klebsiella pneumoniae strain A17KP0038 plasmid pA17KP0038-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

32. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP031803 (Klebsiella pneumoniae strain MSB1_8A-sc-2280397 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

33. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP036194 (Klebsiella pneumoniae strain BA34918 plasmid pIncFIB, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccct	Protospacer
. ****.********* ********. . 

34. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP040026 (Klebsiella pneumoniae strain KPC160132 plasmid pIncFI-L132, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

35. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP028997 (Klebsiella pneumoniae strain AR_0079 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

36. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP027045 (Klebsiella pneumoniae strain 1_GR_13 plasmid IncFIB, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

37. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052281 (Klebsiella pneumoniae strain E16KP0224 plasmid pE16KP0224-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

38. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP012565 (Klebsiella pneumoniae strain UCLAOXA232KP plasmid pUCLAOXA232-4, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

39. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP035909 (Klebsiella pneumoniae strain BA4656 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccct	Protospacer
. ****.********* ********. . 

40. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052423 (Klebsiella pneumoniae strain C16KP0164 plasmid pC16KP0164-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

41. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP024460 (Klebsiella pneumoniae strain QS17-0161 plasmid pMRSN480738_112.7, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttccct	Protospacer
. ****.********* ********. . 

42. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP021714 (Klebsiella pneumoniae strain AR_0129 plasmid tig00000001, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

43. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP026165 (Klebsiella pneumoniae strain F81 plasmid pF81_1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

44. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP015755 (Klebsiella pneumoniae strain W14 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

45. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP016924 (Klebsiella pneumoniae isolate 23 plasmid pIncFIB_DHQP1400954, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

46. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP032187 (Klebsiella pneumoniae strain AR_0075 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

47. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052390 (Klebsiella pneumoniae strain C17KP0052 plasmid pC17KP0052-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

48. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP040597 (Klebsiella pneumoniae subsp. pneumoniae strain KpvST15_NDM plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

49. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052352 (Klebsiella pneumoniae strain D16KP0146 plasmid pD17KP0032-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

50. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NC_016838 (Klebsiella pneumoniae subsp. pneumoniae HS11286 plasmid pKPHS1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

51. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP034055 (Klebsiella pneumoniae strain KP_NORM_BLD_2015_112126 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

52. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052393 (Klebsiella pneumoniae strain C17KP0040 plasmid pC17KP0040-1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

53. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP044370 (Klebsiella pneumoniae strain 2018C01-046 plasmid p2018C01-046-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

54. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP034047 (Klebsiella pneumoniae strain KP_NORM_BLD_2014_104014 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

55. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP016161 (Klebsiella pneumoniae strain TH1 isolate TH1 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

56. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP050276 (Klebsiella pneumoniae strain 10553 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

57. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP052470 (Klebsiella pneumoniae strain C16KP0053 plasmid pC16KP0053-2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

58. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP044046 (Klebsiella pneumoniae strain FDAARGOS_629 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

59. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP050287 (Klebsiella pneumoniae strain 9630 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

60. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_CP032225 (Klebsiella pneumoniae strain AR_0046 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

61. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to NZ_KY354306 (Klebsiella pneumoniae strain 301 plasmid pKP301b, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

62. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to LR134218 (Klebsiella aerogenes strain NCTC10317 genome assembly, plasmid: 2) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

63. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to MK422451 (Klebsiella phage ST13-OXA48phi12.3, complete genome) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

64. spacer 2.1|1080526|29|NZ_CP009279|CRISPRCasFinder matches to CP058330 (Klebsiella phage vB_Kpn_1825-KPC53 chromosome phage_vB_Kpn_1825-KPC53, complete sequence) position: , mismatch: 8, identity: 0.724

aagtttatgctttcgaagtgagttttgta	CRISPR spacer
gcgtttgtgctttcgatgtgagtttcccg	Protospacer
. ****.********* ********. ..

65. spacer 7.1|5657205|34|NZ_CP009279|CRISPRCasFinder matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 10, identity: 0.706

aaagcgtatgcttccgatgttagttttacgcgat	CRISPR spacer
ggagcgtatgcttccgaagtaagtttttgtttgt	Protospacer
..*************** ** ******   . .*

66. spacer 10.1|6083018|37|NZ_CP009279|CRISPRCasFinder matches to AP019525 (Tenacibaculum phage PTm5 DNA, complete genome) position: , mismatch: 10, identity: 0.73

ctactaagttttgtaaagcatatgcatcataggaacg	CRISPR spacer
ctgtattgttttgtaaagcatatgcaccaaaggcatt	Protospacer
**..   *******************.** *** *. 

67. spacer 10.1|6083018|37|NZ_CP009279|CRISPRCasFinder matches to AP019524 (Tenacibaculum phage PTm1 DNA, complete genome) position: , mismatch: 10, identity: 0.73

ctactaagttttgtaaagcatatgcatcataggaacg	CRISPR spacer
ctgtattgttttgtaaagcatatgcaccaaaggcatt	Protospacer
**..   *******************.** *** *. 

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	372861 : 379898	8	Paramecium_bursaria_Chlorella_virus(33.33%)	NA	NA
DBSCAN-SWA_2	730250 : 741713	10	Synechococcus_phage(37.5%)	NA	NA
DBSCAN-SWA_3	2101971 : 2112268	9	Bacillus_phage(83.33%)	NA	NA
DBSCAN-SWA_4	3642319 : 3648967	9	Streptococcus_virus(33.33%)	NA	NA
DBSCAN-SWA_5	3665223 : 3692488	36	Streptococcus_phage(21.43%)	integrase,terminase,portal	attL 3660932:3660946|attR 3696291:3696305
DBSCAN-SWA_6	4730786 : 4738854	9	Staphylococcus_phage(57.14%)	NA	NA
DBSCAN-SWA_7	5298678 : 5309522	10	Hokovirus(16.67%)	tRNA	NA
DBSCAN-SWA_8	6056248 : 6072755	25	Thermus_phage(29.41%)	tail,portal,plate	NA
DBSCAN-SWA_9	6166056 : 6174762	10	Enterobacteria_phage(33.33%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP009279|372861:379898|DBSCAN-SWA
CATGAATCCTAAAGATTTGAACTATACAATGCCACCGGAATGGGGCAAGCATGAACGTACTTTTATCTCCTGGCCGGTGCAGGAATCTATGTGTTTCCCGGACAACCACGAGTCGGTATGCCAAGGTTATGCTGACATTATTACAGCTATTGCCGAGTTTGAACCGATTACGGTCATCGTTAACCCGGAGGACGTGGAAAAGGTAGAACGTCTGGTCAGCGGACCGAATGTAACGCTACTACCTATAAAGCATAGCGATGCTTGGTTGCGTGATAACGGGCCTACCTTTGTTGTTAATAAAGACGGCGTTCTAGCAGGTGTGAACTGGAAGTTTAATGCCTGGGGCGGTAAATATTCACCTTGGGATCTGGATGATGAGGTAGCTCCACAGATTCTCGAACACACACAAGTGACACGCTTTGATGCGCCGCTTGTGATGGAAGGCGGCTCGATCCATACGGATGGAGAAGGCACCTTGATTACTACAGAAGAATGTCTGCTCAATACGAACCGCAACCCGGATTTGAAGCGCGAGAATATTGAAGAGTACGTGCGCAATTATACAGGTACAGAAACTATTATCTGGCTTAAGCGTGGTCTAAGTGGTGATGAAACCGATGGTCATGTGGATAATATCGCTTGCTTCGCTGCTCCAGGTAAAGTCATTATTCAGGTCTGTGAGGATCCGCAGGACGAGAATTTTGAGATTACACAGGAGAATCTTCGTATTTTGGAGAATGCCATAGATGCCAAAGGGCGTAAGCTGGAGATCATCAAGATTCAGCAACCACCACGGGTGGATCATGACGGCAGCCGTCTGACGCTCAGTTATTTGAACTTCTATTTCGTAAATGGTGGAATTATTTTACCTGTGTTTGGCGGTACAGCGGTGGAAACAGATAAACTTGCCGAGGAAGTACTGGCTGGTTTGTTCCCGGAACGTAAGATTCGTACAGTTAACGGTATGGCGGTCATCACCGAGGGCGGGAACGTTCACTGCACTACGCAGCAAATGCCTGCTCAGCAATAATTGAAGGAAACTAAACGTCCAAAGGGACATTTATATATAAGGAGGACAGATTCTTGAGAAATGTAAAAGTAGCTGCGACGCAAATGAGCTGTTCCAGCAATATTGATGAGAATATCAGTAAAGCCGAAACATTGGTCAGAGAAGCGGCGGCACAGGGAGCACAAATTATTTTGCTGCAGGAGCTGTTCGAGACTCCGTATTTCTGCCAGAAAGAGAAAGCTGATTATTACGCATATGCAACAGAGCTTGAGCATAACAAAGCGATTAATCATTTCACAGCAATAGCCAAGGAACTGCAAGTGGTGCTGCCAATCAGTTTTTATGAGAAAAAGAACTACGCACGTTACAACTCACTAGCTGTAATCGATGCCGATGGAACGATACTGGGCAAATACCGCAAGAGCCATATTCCAGATGGCCCAGGGTATGAAGAGAAATTCTACTTCAATCCGGGAGATACTGGCTTTAAAGTATGGAACACTCGCTATGCCAAGATTGGTGTAGGGATTTGCTGGGATCAGTGGTACCCGGAAGCGGCTAGAGTGATGAGCCTGATGGGAGCAGAAATTCTGTTCTATCCAACCGCTATCGGATCAGAACCACAGGATGGATCGATCGACTCTAAGGATCATTGGCAGACTTGTATGCTTGGGCATGCAGCGGCTAACCTTATTCCAGTCGTTGCCTCCAACCGTATTGGTGAAGAGATTGATGAAGATTCTAGCATTAATTTCTACGGCTCTTCGTTCATTGCGGGACCGCAAGGCAATAAAATTGTTGAAGCAGGCCGAGACGAGCAAGCTGTAATAGTGAGCGAATTTGATCTGGATGCTTTGGAAGTCGGACGGATCGAGTGGGGCGTCTTCCGTGATCGCCGGCCGGAGCTGTACAAAATGATTGGTTCTTATGATGGGGACATCATTCTTTAAAAGAATTCACAGTTAAATGTGCTAAAGGCATTGCTAGAGAGGATAGAATCTCTGGCAGTGCCTTTTTTGGTGTTTCAACGAGAAATACGGGGGTTCTTTGAACAGAGGAGCAATTGTTCGGAAATCCTGTGCAAGATCGGACACAATCTTTTCTATCAAAAGTGCTGTAAAAGTCTGGAAAAGTAGAATATTGATATTTTATCAGGTATATTAGAAGAGTAAACCGTGATTCAGGGATCTACTATGAAAATTCTGTCGGATACGTGGAGAGGAGGCTCTGGGATATCTTTTGTTATCATAATCTTGCAGTGATAGAAGGAGAAAACGATGAGCACATTTAAAAACTGGTTGAACACAACCAAAAACGGACTAACAGAACAAGTAAAGAAATTCAAAAATAAAGATTTCATGAATGCGGTAGTTGCGGGCTGCGCCTTGGTTGCTGCTGCCGACGGTAAAATAGAAGAAGCTGAAAAGAATAAAATGGCTGGTTACATGAATATGAGTAATGAGCTTAAGGTGTTTGACATGAGAGATGTAATTACCCAGTTCAACTTTTATGTAAGTAACTTTGAGTTCTCACCAGAAATCGGTAAGCAGGAAGCACTGAAAGCAATCGGTAAGTTTACCGGTAAACCAGATGTGGGACGTGTAATTGTGGGTGTGTGCTCAGCTATTGGATCAGCTGATGGTGATTTTGATGACAATGAAAAAGCAGTTGTGCGGCATATTTGCGGTGTCTTGGGATTAAACCCTGGTGAATTCAGTTTATAAATGATGTAATACCATATACATGAGTTCGGATGAAACGTATTTAGTTCTTTAGCGTATCACTCATATAACATCCAAAAGCTAGACTAATAGATGGTGATTCTTTTTAGGGAATGGAGGTACGTAAAGTTGGCTGGAATTAATCTGGTAAAAGGTCAGAAGATTGATCTCACAAAAGGTAATGCAGGCTTATCTAACGTAATTGTAGGTTTAGGTTGGGATCCGGCTGAGCCAGCTCGAGGATTCTTCGGTGTGAAGAAACAGGCCAACGTGGACTGTGACGCTTCAGCACTGATGCTGAACGAGAATGGTAAGCTAGTTAAGAAGGGTAACCTGGTGTGCTTCCATAACAAGCAAAGTCCTTGTAACTCTGTCATTCACTCCGGAGACAATCTCACGGGTGATGGTGACGGAGACGATGAGCAAATCATGGTTAACCTGAATGCCATTCCTTCCGATGTACACAAGGTTCTGGTAGTTGTGAATATTTATGATGCCACGAACCGTAAACAGGATTTCGGATTGATTAAGTCAGCTTATATCCGTGTGATAAACGCTGTAGGCAACAATGAGCTAATCCGTTTCAACCTATCTGATAATTACAATGGCTATACGGCGCTTATTTGTGGGGAACTTTACCGTCAAGGTGGAGAGTGGAAGTTCGCCGCAATTGGTGAGGGTAGTCACGCGGCACATATCAATCAACTGGCAGAACGCTACGTATAATCCAAATAAAAGAAAAGAGGAATGTTATCATGGCAATTAATCTATCCAAAGGTCAAAAGATCGATTTAACAAAAACAAATCCAGGTCTATCCAAAATCACAGTAGGTCTTGGTTGGGACACTAATAAATATGACGGCGGTAAAGATTTCGACTTGGACGTTTCCGTATTCTTGACTAATGCGAACAGCAAAGTTGAAAAAGAAACCAACTTCATTTACTTCAATAATAAACAGAACGAGAACGCTTCTGTTGTTCATACAGGTGATAACCGTACGGGTGACGGCGATGGTGATGATGAGCAGATTCAAGTGGATCTTCTGAGTATCCCAGCGGATGTAGAAAAGGTAGCTTTTACTATTACAATTTATGAAGCTGAAACAAGAAGCCAAAACTTCGGTCAAGTTTCTCGTTCTTATGTACGTATCGTAAATGATTTGAACAATGAAGAACTAATCCGTTTTGATTTGGGTGAAGACTTCTCTATTGAAACTGGCGTTGTTGTCGGTGAATTGTACCGTCATGGTGCAGAGTGGAAGTTCAATGCAATCGGTAGCGGCTACAAAGACGGCTTGAGCGGTTTGACTCGCGATTACGGCTTGCAATAAATCTTGAAGTATAAATCTTGTAGTATAAATCTTGTAGTACACAGTGAATTGAATCCACTCACGAAAGAAGGTTATGTCAGTGACGATCAGTCTTTCCAAAGGACAGCGGATTGATCTTACCAAGACTAATCCAGGTCTGACAAAGGTAGTAGTTGGATTGGGCTGGGACACTAATAAGTATAGTGGAGGTCAAGATTTTGACCTCGATGCTTCAGCGTTTCTGCTTCATGAAGACGGCAAAGCTAAAGGTGCAGATGATTTTGTATTCTATAACAACCCAAATGGTGGCGCAGGCTCTGTAGTCTACACGGGAGATAACCGTACGGGAGAAGGCGACGGAGATGACGAGCAAATTATCGTTGATTTCAGCAAAGTCCCTACCCATATTCAGCGTATCGGTATAACCGTAACGATTTATGATTACGAAACTCGTGCACAGAACTTTGGACAAGTCTCCAATGCTTTCGTACGTGTGGTTGATGCTTCCACAGATCGCGAAGTACTCCGTTTCGACCTGGGTGAAGATTTCTCAACAGAGACGGCAGTTGTATTCTGCGAATTCTACCGCAATGGTGCGGATTGGAAATTCCAGGCAATCGGTAGTGGTTTTGGCGGCGGCCTTAGCGCATTGTGTAAAAATTATGGGCTGGACGCGCAATAGCATCTTCCGGGCGGGGTCATCACCGATCCTGCCCTTTTTTTAATTCTTTATGGATTGCCTCACAAAGGAAATGGAATGGGTCTCGAAGTATAAACTCCACTTTGTGGGGTTATTTGAAAATACAAGAAAGCAAAAGTTTCACACGATACTATATGAATTATATTTCTCGCTTAAACGCTTGCCGTCCTTATAAGGACACCGAAGGCGTTATGATTGCTCCATTTATAAAGGTGGTGTAAGAATGGGTATTACAGTTGTCAAAGGACAAAAGGTTGATTTAACTAAAGGGAATCCTGGACTTGATTCTCTTATCGTAGAGATTGGCTGGCAATCGCCATCTTCACTTGAGATTGATACTTCTGCTTTTCTGCTTGGAGCGCAAGGTAAAGTAAGCAAAGATGAGGATTTGATATTTTATAATAATCCGTCTACACCTTATATCAGATATAAGGAAATGCCTACATCAAACAGCCTCAAGCAATTTGACGTGGAACTAAACAAAGTTCCTTCTGATGTGATGAAACTCGCGTTTACACTTACCATTTATGATGGCGAGAAGCGGGGTCAAAGCTTTAGGCAGGTAAATCAGGCCTATTTTCGGATTCTGAATCAAGTAACAGGTGCGGAGCTTCTCCGATGTGATCTTGAAAATCATTTCTCCGTGGAAACGGCTGTTGTGGTAGGAGAATTATATAGATATAACGGTGAATGGAAATTCAGCGCCATAGCCGCGGGTTTTGCTGGTGGTCTACAGGAACTGTGTAGGAACTTTGGGATAGAAGCGAACGATGAACCGGCACCGACACCGACACCAATACCAGTGCCTAAGCCTGCTGCTCCGCCGCAGCCAGAGCTTAAACGTCAATCAGCGCCGGTAGCGGAGCCTAAGATTCAGATTCCACCTCCTCCTGCAGCTGCGCCTTCACCTGTAACACCCCCTCCGGTCAATCTCAACCTGAAGAAGATCGAACTGAAGAAAAAAGGTGATTCGATCAACCTGAAGAAATCAGCTGGTGGTTTGGGCGAATTGCTAATTAACCTCAACTGGAATCAGAAGCAGGGTGGAGGGCTATTTAATCGTAAAAATGGTGTGGATTTAGATCTTGCTTGTCTATATGAGTTGAAGAATGGTAGTAAGGGAGTAGTTCAGGCGCTGGGCAATGCTTTTGGCTCATTGAACCAACCTCCTTATGTCTTGCTTGATGGAGATGACCGGACAGGCTCTGTAACAACCGGTGAGAATCTGCGGATTAATGGCAGCAAAATTGCTGATATTGAACGGATTCTAATTTTTTCTTTTATTTATAAGGGTGTTACCAATTGGTCAGAAGCTGACGGTGTTGTCACGATTACCCAGAGTGGTGGCCCCGATATTATTGTCAATTTGGACGAGCATAACAACCGCAAAGGCATGTGTGCCATCGCGTTATTTCGGAATGTGAATAACGAGACATTCAGTGTTGAACGGCTGGTCCAATATTACAGTGGTCATCGGGAGATTGATGAGGCATATGGTTGGGGACTGCGCTGGGTTGCTGGCAGTAAATAGACGATTTTTTCGGAGGCGCAAGTGTAATGGATTGGTTCGCTGATTTTTTCAGGAATATTAGTGAGAACTACGGTCATTTTTTCTCATGGAGCGATGTGGTAGGTACGCTCTCAGACCCGGTTAGCTGGGGCATTATTGGTAGCTTAGTGCTACTAGAAGGGCTGCTCTCTGCAGATAATGCGCTTGTTCTCGCCGTCATGGTTAAGCATTTACCTAAAGAACAACAGAAGAAGGCGCTCTTTTACGGTATTATAGGAGCTTATGTATTCAGATTTTTGGCTATCGGTCTAGGGACATTTCTTATTAAATTCATGTTGGTTAAGGTTCTTGGTGCAGCCTATCTCTTTTATATCGCTTATGGCGGGTTATTTAAGGGCGGTGGCGATGAGAAGATCGAGAACAAGGGGTTCTCTTTTTGGAAGACGGTTCTCCTTGTTGAATTAATGGATATTGCTTTTAGTATTGATAGTGTTATTGCTGCATTTGGTGTTAGTAACCAGGTTTGGGTGCTCTTTATGGGCGGAATCATAGGCGTTCTGATGATGCGGGGAGTAGCGCAATTATTCTTGAAGCTTATTGATAAAATTCCGGAACTCGAGCGTGCCGCTTTTGCGCTTATTGCCATTATTGCTGGTAAAATGCTCGCGGGCGCTTTTGGGTACGAAATGCCACATGTATTATTCTTTTCAATCATTATTCTTGTATTCGGTGGTACGATCCTTTACAGCGTACTGCGTAAGAAAAAAGAAGCCCATAGAAATGCTTGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP009279|372861:379898|377823_379131_+|WP_042184264.1|DBSCAN-SWA
MGITVVKGQKVDLTKGNPGLDSLIVEIGWQSPSSLEIDTSAFLLGAQGKVSKDEDLIFYNNPSTPYIRYKEMPTSNSLKQFDVELNKVPSDVMKLAFTLTIYDGEKRGQSFRQVNQAYFRILNQVTGAELLRCDLENHFSVETAVVVGELYRYNGEWKFSAIAAGFAGGLQELCRNFGIEANDEPAPTPTPIPVPKPAAPPQPELKRQSAPVAEPKIQIPPPPAAAPSPVTPPPVNLNLKKIELKKKGDSINLKKSAGGLGELLINLNWNQKQGGGLFNRKNGVDLDLACLYELKNGSKGVVQALGNAFGSLNQPPYVLLDGDDRTGSVTTGENLRINGSKIADIERILIFSFIYKGVTNWSEADGVVTITQSGGPDIIVNLDEHNNRKGMCAIALFRNVNNETFSVERLVQYYSGHREIDEAYGWGLRWVAGSK
>NZ_CP009279|372861:379898|375719_376316_+|WP_042184259.1|DBSCAN-SWA
MAGINLVKGQKIDLTKGNAGLSNVIVGLGWDPAEPARGFFGVKKQANVDCDASALMLNENGKLVKKGNLVCFHNKQSPCNSVIHSGDNLTGDGDGDDEQIMVNLNAIPSDVHKVLVVVNIYDATNRKQDFGLIKSAYIRVINAVGNNELIRFNLSDNYNGYTALICGELYRQGGEWKFAAIGEGSHAAHINQLAERYV
>NZ_CP009279|372861:379898|376345_376921_+|WP_042184261.1|DBSCAN-SWA
MAINLSKGQKIDLTKTNPGLSKITVGLGWDTNKYDGGKDFDLDVSVFLTNANSKVEKETNFIYFNNKQNENASVVHTGDNRTGDGDGDDEQIQVDLLSIPADVEKVAFTITIYEAETRSQNFGQVSRSYVRIVNDLNNEELIRFDLGEDFSIETGVVVGELYRHGAEWKFNAIGSGYKDGLSGLTRDYGLQ
>NZ_CP009279|372861:379898|372861_373890_+|WP_042184254.1|DBSCAN-SWA
MNPKDLNYTMPPEWGKHERTFISWPVQESMCFPDNHESVCQGYADIITAIAEFEPITVIVNPEDVEKVERLVSGPNVTLLPIKHSDAWLRDNGPTFVVNKDGVLAGVNWKFNAWGGKYSPWDLDDEVAPQILEHTQVTRFDAPLVMEGGSIHTDGEGTLITTEECLLNTNRNPDLKRENIEEYVRNYTGTETIIWLKRGLSGDETDGHVDNIACFAAPGKVIIQVCEDPQDENFEITQENLRILENAIDAKGRKLEIIKIQQPPRVDHDGSRLTLSYLNFYFVNGGIILPVFGGTAVETDKLAEEVLAGLFPERKIRTVNGMAVITEGGNVHCTTQQMPAQQ
>NZ_CP009279|372861:379898|377000_377582_+|WP_042184263.1|DBSCAN-SWA
MTISLSKGQRIDLTKTNPGLTKVVVGLGWDTNKYSGGQDFDLDASAFLLHEDGKAKGADDFVFYNNPNGGAGSVVYTGDNRTGEGDGDDEQIIVDFSKVPTHIQRIGITVTIYDYETRAQNFGQVSNAFVRVVDASTDREVLRFDLGEDFSTETAVVFCEFYRNGADWKFQAIGSGFGGGLSALCKNYGLDAQ
>NZ_CP009279|372861:379898|373943_374819_+|WP_042184256.1|DBSCAN-SWA
MRNVKVAATQMSCSSNIDENISKAETLVREAAAQGAQIILLQELFETPYFCQKEKADYYAYATELEHNKAINHFTAIAKELQVVLPISFYEKKNYARYNSLAVIDADGTILGKYRKSHIPDGPGYEEKFYFNPGDTGFKVWNTRYAKIGVGICWDQWYPEAARVMSLMGAEILFYPTAIGSEPQDGSIDSKDHWQTCMLGHAAANLIPVVASNRIGEEIDEDSSINFYGSSFIAGPQGNKIVEAGRDEQAVIVSEFDLDALEVGRIEWGVFRDRRPELYKMIGSYDGDIIL
>NZ_CP009279|372861:379898|375146_375593_+|WP_042184258.1|DBSCAN-SWA
MSTFKNWLNTTKNGLTEQVKKFKNKDFMNAVVAGCALVAAADGKIEEAEKNKMAGYMNMSNELKVFDMRDVITQFNFYVSNFEFSPEIGKQEALKAIGKFTGKPDVGRVIVGVCSAIGSADGDFDDNEKAVVRHICGVLGLNPGEFSL
>NZ_CP009279|372861:379898|379157_379898_+|WP_042123539.1|DBSCAN-SWA
MDWFADFFRNISENYGHFFSWSDVVGTLSDPVSWGIIGSLVLLEGLLSADNALVLAVMVKHLPKEQQKKALFYGIIGAYVFRFLAIGLGTFLIKFMLVKVLGAAYLFYIAYGGLFKGGGDEKIENKGFSFWKTVLLVELMDIAFSIDSVIAAFGVSNQVWVLFMGGIIGVLMMRGVAQLFLKLIDKIPELERAAFALIAIIAGKMLAGAFGYEMPHVLFFSIIILVFGGTILYSVLRKKKEAHRNA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042184254.1|372861_373890_+	agmatine deiminase family protein	A7RCL2	Paramecium_bursaria_Chlorella_virus	1.8e-66	37.9
WP_042184256.1|373943_374819_+	N-carbamoylputrescine amidase	M1GUG4	Paramecium_bursaria_Chlorella_virus	7.4e-74	47.6
WP_042184258.1|375146_375593_+	tellurite resistance TerB family protein	A0A1Y0T181	Sinorhizobium_phage	2.0e-06	28.6
WP_042184259.1|375719_376316_+	TerD family protein	K4JRX3	Caulobacter_phage	1.4e-23	34.7
WP_042184261.1|376345_376921_+	TerD family protein	NA	NA	NA	NA
WP_042184263.1|377000_377582_+	TerD family protein	K4JRX3	Caulobacter_phage	1.7e-26	36.1
WP_042184264.1|377823_379131_+	tellurium resistance protein TerA	NA	NA	NA	NA
WP_042123539.1|379157_379898_+	DUF475 domain-containing protein	A0A068EP98	Bacillus_phage	4.1e-57	52.0

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP009279|730250:741713|DBSCAN-SWA
TATGATCGAACGTTACAGCAGACCTGAGATGCGAGCTATTTGGACGGAGGAAAATAAATTCAAGGCGTGGCTGGAAGTTGAAATTTGCGCTTGTGAAGCATGGGCTGAGCTCGGAGTCATCCCGCACGAAGACGCAGCTAAACTGCGTAAAGACGCTAAATTCGACATCGCACGCATTGATGAAATAGAACAAGAGACTCGCCATGACGTTATCGCCTTTACTCGTGCGGTTTCCGAGAGTCTTGGCGCAGAGCGCAAATGGGTTCACTACGGTCTTACTTCTACTGACGTGGTAGATACGGCGCTAGGTTACTTGCTGCGTCAAGCGAATGAAATTCTAGAGAAGGATATCATCAACTTTATTGAGATCCTTAAAGATAAAGCTATTGCTTACAAGGATACACCGATGATGGGCCGTACGCATGGTGTTCATGCCGAGCCAACTACCTTTGGTCTGAAAATGGCTCTATGGTACGAAGAAATGAAACGTAACCTGGAGCGTTTCCGCCATGCTGCGAACGGTGTACAGTTCGGAAAAATCTCCGGTGCCGTTGGTACGTACGCTAACATCGATCCTTTCGTAGAAGAATTCGTTTGCCGCAAGCTCGGCACAAGCCCAGCTCCAATCTCTACACAAACGTTACAGCGTGACCGTCATGCTGAATTCATGGCTGCTCTTGCTTTGGTAGCGACATCGTTAGACAAATTCGCTACTGAAATCCGCGCTCTGCAAAAGAGTGAGATTCGTGAAGTGGAAGAAGCCTTTGCCAAAGGTCAAAAGGGTTCATCCGCTATGCCTCACAAACGGAATCCGATCGGCTGCGAGAACATTTCCGGTCTGTCCCGCGTCATTCGCGGACATATGGTTACAGCTTATGAGAACGTGCCACTCTGGCATGAACGCGATATTTCGCACTCCTCTGTGGAACGTATCATCCTTCCGGATGCGACAATGCTGCTCAACTACATGCTGAACCGTTTCGGTAACATCGTGAAGAACCTGACTGTATTCCCAGAGAACATGAAGCGTAACATGAACCGTACGTTCGGTGTTCCTTTCTCCGGTCGGATCTTGACTAAACTGATCGATAAAGGCCTTAGCCGTGAGCAAGCGTACGATACCGTTCAACCGCGTGCTATGCAAGCTTGGGAAGAGCAAAAACAATTCCGCGATATCGTGGAAGCTACACCTGAGATCACTAACGTTCTTACCCCAGAAGAAATTGAAGATGCATTTAACCCTTCTTGGCACCTTAAGCATGTGGACACCATCTTCCGCAAGCTAGAGCTGCTCTAAAAAATAGGTGCGTTAATGGTTGGGTCGATAAGGAACGAATTCCTCGGAATGAGACCTTAGAGATCCTAAAAAGATAAGTTAGTGGTGAACTAAGGAACGCTGCAATAAATGCAAAGCTGGATGGGGGAGCACTGTAGAGGAAGTTTGGAACTGTAGAAGCGTAGCGTTCGCCTTTATCCTCGGATTTCTACCGCGAGAAGCGGTTCAAATCAAGAAATCTGAGGATAACAGCGATCGGAAGTCCGAACATTCCTCGGAAGAGCTTCCTCCTAGACCAGCCCAACTTAGGAAGATCATTAGTTCAAGGGAGGAAAGGTCATGACATCGTCGGCCGTATCCACAGCCGTGGAACTCATCAATGCGCCGCTGCTCTATAAAGGGAAGGTTCGTGAGCTATACGATTTAGGGGAGAATGTACTGATCGTCGTCACGGATCGGATATCTGCTTTTGACTATGTGCTGGACCCAGCGGTACCTGAAAAGGGCAATGTGCTTAACCGTCTGAGTGCGTTCTGGTTCGGAAAGACCAAAGAGCTAATGGAGAATCATGTCGTTCATATCGATGTGGATCTGCTCGGAGATATCGTTAAGGACAAGGAAGCTCTCAGAAACCGTGTTATGGTAGTACACAAAGCAGAGCGCATCGATATCGAATGTGTTGTGCGTGGGTGCATCACCGGTGGGGGCTGGAGACAGTATCAAGAAACTGGCAAAGTGAATGGTATTGAGCTTCCTAAGAACTTGCGCAAAAATGCGCTGCTGGCACAGCCAATCTTTACCCCTGCGGCTAAAAACGATGTAGGTCATGATGAGGATATTCCTTTTGAAAAGATGCAGGAGCTAATCGGTGCTGATCTGGCACTCGAGCTGCAGGAGAAGAGCTTGCAATTGTTCTCTTTTGCCAGAGAGTATTGTGCTGAGCGGGGAATCATTTTAGCAGATTGTAAATTTGAATTCGGCTTGCTGGATGGCAGGGTGATTCTGATTGATGAGATTTTTACGCCGGATGCTTCACGTTTCTGGGCCAAGGACAAATACGTTCTTGATATCGAAATTGATAGTATGGATAAAGAACCTGTTCGTACGTATCTATCTGCATCCTCCTGGGATAAAAATAGCAAACCTGATCCACTTCCACTAGAAGTAGTTGAAGAAACAACGCGCCGTTATCTGGACATTTATCATCGTCTTACTGGCAAGTCTTTATAGCTCAACATTGTGTGTTTACTCATGGGAATAAATGAAGTGTATGTTTTTAAAGCTAGAGTTACTTTTAGTAGAGTTTCAGCTTTCAGAAAGTATATACACATAAAAATTTAGGAGGAACTACAAGCATATGTTAAAAGCGACGGTATATGTCACCATTAAGAAGAGCGTTCTCGATCCACAAGGTGTAGCAGTGCAAGGAGCACTTCATTCGGTAGGTTTTCAAGAAGTTGAAAGTTTGCGTATTGGGAAATATATGGAGCTGACTTTGGACACGGATAACCGTGCTGAAGCAGAAGTGCGTCTCAAGGAAATGTGCGAAAAGCTACTTGCCAACACGGTGATCGAGGATTACCGCTACGAATTGGAGGACTAAACGACATGAAATTTGCTGTACTTGTCTTCCCAGGCTCTAACTGTGATATTGATTGCTACAAGGCGGTAGAGGACAGTCTCGGCGAACCAGTCGATTATGTGTGGCATACAGCGACAGATTTGTCGGCGTATGATTGCATTTTGGTTCCAGGCGGATTCTCATATGGTGATTACCTGCGCTGCGGCGCGATTTCAAGATTTGCTCCTGTAATGGCTGAAGTTGCTAAAGCAGCAGAGCAAGGAAAATTCGTGCTAGGCATTTGCAATGGGTTCCAAATTCTTACTGAGGCTGGTTTGTTGCCAGGCGCGCTGCGTCGTAACATGTCCATGAAGTTCCGTTGTCATGATACAGTGCTTAAGGTTGTTAATAACGAAACCCCATTTACTATTGATTATGCTAAGGATGAAGAAATCATCATCCCAATCGCTCACGGCGAAGGAAACTATTACTGTGATGAAGAGACTTTAGCAGAACTGAAAGCTAACAATCAGATTGTGTTCACATATAGCGATAATCCTAACGGCTCTGTAGCTGATATTGCGGGTGTTAGTAATGTGCAAGGGAATGTAGTCGGCATGATGCCTCACCCTGAGCGTGCAGCTAACAGCTTGCTCGGATCTGAAGATGGCAAACGAATGTTCACATCTATACTGAAGACTTGGAGGGATCGTCATGACGCAGCAAGTATCCGTTAAGGAACCGACCGCAGAACAGATCGCAGAGCAGAAAATTTACAGCCAATTCGGTGTGTCGGACAGCGAATATGAGCTCATCAAGTCTTTTATGGGACGTTTGCCGAACTATACTGAAATCGGCGTATTCAGCGTAATGTGGTCCGAACACTGTGCATACAAGAACTCTAAGCCATTGTTGAAACGTTTCCCAGTTACTGGACCACGTGTCCTGATGGGACCCGGCGAGGGCGCAGGGATTGTAGATATCGGAGACAACCAAGCGGTTGTATTCAAAATCGAAAGTCATAACCACCCCTCTGCGGTAGAACCTTTTCAAGGTGCGGCAACAGGCGTAGGTGGTATCATTCGTGATATTTTTTCCATGGGCTCAAGACCTATCGCACTGCTGAATTCCTTGCGTTTCGGCAAGCTGGAAAGCGATCGCGTGAAATATTTGTTCGAGCATGTCGTGTCTGGTATTGCTGGCTATGGTAACTGTATCGGGATTCCAACCGTGGGCGGCGAAATCATGTTCGATGATAGCTATGACGGTAACCCGCTTGTTAATGCAATGTGTGTCGGTCTGATTGATCATGATAAAATCCAGCGTGGTGTCGCTAAAGGTGTAGGAAACCCAGTCTTCTACGTAGGTCCTCCTACTGGACGTGATGGGATTCATGGGGCTACTTTTGCATCCGTTGAACTAAGTGAAGAGTCCGAAGCAAAACGTACAGCTGTACAAGTAGGCGATCCATTTATGGAGAAGCTCGTTATGGAATCTTGTCTAGAGTTAATCGACAGCGGCATTGTTATTGGGATTCAGGATATGGGTGCGGCTGGACTTACCTGCTCTAGTGCAGAGATGGCAAGTAAAGCTGGTAATGGTTTGGAGCTGTATCTTGATCAGGTGCCACAACGTGAAGACGGCATGACCCCTTATGAAATGATGCTTTCGGAATCGCAAGAACGGATGTTGTTTGTAGTAGAACCGAAGGATGAAGCTCAGGCGCAAGAGATCTTTGATCGCTGGGGTGTAATCTGCTGTAAGGTAGGTAAAGTAACGGATGATGGTCGCTTGAAGCTGTATCATCACGGTGAGGTTGTTGGCGACATGCCTGTAACAGCGCTCGTGGATGAGTGTCCAGTGTATAATAAACCATCTGAGGTTCCTGCTTATTATGTAGAAAATGAATCGGTAGACACGCTTCGTTACGCGGAAGTTACAGATCTGGGTAGCGCACTGCGTACAGTGCTTGGATCACCAACCGTAGCAAGCAAAGCTTGGGTATACAACCAATATGATTACATGGTTCGGACTAGTACGGCTGTTCGACCTGGATCTGATGCGGCTGTAGTTACCATTCATGGTACACGTAAAGGACTTGCGATGACCACGGATTGTAACGGGCGTTATGTTTATCTTGATCCTGAAGTGGGCGGACGGATTGCAGTCAGCGAAGCGGCTCGTAACATCGTTTGTTCGGGTGCTGAACCGCTTGCTATTACCGATAACCTAAACTTCGGAAACCCTGAGAAACCTGATGTGTTCTGGCAAATGGAGCGTGCGGTTGATGGTATGGCTGAAGCTTGTCGTGTGCTGGATACTCCGGTTATCGGCGGGAATGTCAGTCTTTATAACGAAAATACGACGGGATCCATTTACCCAACGCCGGTTGTCGGCATGGTTGGTTTAGTAACGGATACGGATCATATTACGACTCAAGGCTTCAAACAAGAAGGAGATTCCATTCTTCTGCTAGGCGTAACAAAAGCTGAGCTTGGTGGTAGTGAATTTCAATATGCTGTTCATGGTGTAACCGAAGGCCGCCCTCCAGCTTTGGATTTGGCTACTGAGAAAACACTGCTGAGCACAGTGCTTACCTCGATTCGCGGCGGTCTGGTGCGTTCAGCACATGACTTGTCCGAAGGCGGCCTTGCTGTAGCACTTGCAGAGAGCTGTATCAGTGGTGGTATTGGTGCGAACGTTGAACTTTCTGCTAATGGACTTAGATCCGATATAGCATTGTTCAGTGAGAGCCAATCACGTATCGTGCTGACGGCAGCACCTGAACGTGCGGAAGAGCTGAAAGCAGCGATTGCTGCCAGCGGCGTTCCAGTGGAAATCATCGGAACTGTAGGTGGAGACAGACTGCGCGTAAATCTGGACGGTGCATCCGTATTAGATGAAGCTGTAGCAGAATTGAAATTCGTTTGGGAGGATGCTATTCCATGTCTTATGAAATAAAGACCGGGAAAGAGCAGGAGACTCCTATCCTGTGGACTGGTGACTTTTACAATGAAGGAACGGGCTCGGGAGATATTTTTGACACATTAAAAGAAGAATGCGGCGTTTTCGGGGTCTTCGGACACCCGGAAGCGGCGTCCATGTCTTATTACGGCTTGCACGCCTTACAGCACCGTGGGGAAGAAAGTGCGGGCATCTGCGTAGCAGATGGTCGTGATTTCAACTATCACCGCGGGATGGGGTTAGTAAAAGAAGTATTCGACAAGGACAAAATTGCCTCACTGGTTGGAGACATGTCCATCGGGCATGTACGTTATTCCACCAGCGGAGACAGCCGCTTAACCAATGCACAGCCGCTCGTATTCAAATATCGTGACGGTGATTTGGCGATTGCTACGAACGGTAACATAGTAAATGAACCGTTGATTCGTAAACAGCTTGAGCAAAGCGGATCAATCTTCCAAACCACAAGTGATACAGAAGTGCTGGCGCATCTGATTGCGCGTTCGTCTAAGGATTTTGTTGAAGCGGCTAAGGATGCGCTAAAACAACTGGTTGGCGGATTTGCTTTTCTGCTTATGACGAATGACAAATTAATTGTCGCTTCGGATTCCCATGGTTTGCGTCCGCTTGTAATGGGACGGATCGGCGACGCCTATATTTTTGCTTCCGAATCTTGCGCCTTAGAAGTTATCGGAGCACAGTTAGTACGCGATATCGAACCTGGCGAACTGCTCGTGCTTGATAAAAATGGCCTGTTAGAGGACCGTTTTACCGAGCCAAAACGTAAAGCGCTATGCGCGATGGAGTATATTTACTTCTCTCGCCCAGACAGTGATATGAATGGCGCTAACCTGCACACCGCCCGTAAGCGGATGGGTAGCCGAATGGCATTAGAAGCTTTCGTAGATGCTGACCTCGTAACTGGTGTACCGGATTCAAGTATCTCGGCAGCGATTGGATTTGCGGAGCAGACGGGCATTCCTTATGAGCTTGGGCTCATCAAGAATAAGTATACAGGCCGGACCTTCATCCAGCCGAGCCAAGAGCTGCGTGAGCAAGGTGTGAAAATGAAGCTAAGCGCCGTGCGCAGTGTGGTCGATGGCAAACGTGTTGTCATGATCGATGATTCCATCGTGCGTGGAACAACTTCACGGCGGATCGTCAATCTGCTCCGTGAAGCGGGAGCCGCAGAGGTTCACGTGCGGATTACATCGCCGCCCTTCAAGAATCCTTGCTTCTACGGCATTGATACCCCAGACCGCCGCGATCTCATCGCGTCGTACAAGTCCATTGCGGAAATGTGCGAAGAGATTAATGCCGATTCCTTGGCATTCTTGTCACCGGAGGGTTTAATCACTTCCATTGGTGGTCACAACAAAGATGATTACAAAGGCGGGCTATGCCTTTCCTGCTTCGATAATGATTACCCGACGCAGGTTGATTTTGACGGGGCGGAAAAAGATGGCTGCTCATGTTGACATCCCCCTAAGTCCCCCTTGCAAAGGGGGATTCCGAAGGGCTCTGCCCTCCGGCCACCCGAAAGCTCGGCGGTAGGAGTTGGGTTATAACTTGCTAAGAAGACTTGGGTACGAGTGCTCGCTTTGTCCCTGTGTGCTACGCACGGACGGGACACGCTTTACGGCGCTCCGCCCCCCGGCTGCATACCGCCGCCGGGAATGGCTCGCCAAGCTGGTCGCTAGTCTCGCTAAGGTAGGCGCTCGGCTACGCCCAAAGCGCCAAGAGCAGCTCACCAAGCTCGTCCCTGTTTGCTGCGCAAATGCAGGACTCGCTTGTCTCGCTAAGGTAGGCGCTCGACTGCGCCCAAAGCGTCAAGAGCAGCTCGCCAAGCTCGTCCCTGTTTGCTGCGCAAATGCGGAACCCGCTAGTCTCGCTAAGGTAGGCGCTCGGCTGCGCCCAAAGCGCCAAGAGCAGCTCACCAAGCTCGTCCCTGTTTGCTGCGCAAATGCAGGACCCGCTTGTTTCGCTTAAGGAGGTGCATGGCGCAGCTCATGCACCGAGGTCTTGAGGTCCGTGTGCAAGGCGCGCACTGCGGCTTGCAGTAGGGTGAAAGCGGTGGTTGGAGGGAGTTATGGAGAGGAAGTTTGGAACTGTAGAAGCGTAGCGCTCGCCTTTATGTTTGGATTTCTACCGCGAAGAGCGGTTTAAATCAGGAAATCCAAACATAACAGCGATCGGAAGTCCAAACATTCCTTGTAATAGCTCCCCTATAACCACCAAAAAAATCCCGAATGCCCCACAAACGCGCTCTAAATTAAAATAAGATGAGGTGTCCCAAGTGTCGGAAGCTTATAAAAACGCCGGAGTGGATATTGCGGCTGGTAACGAAGCGGTAGAACGCATGAAAAAGCACGTAAAACGTACTTACCGTCCAGAAGTAATGACGGATCTTGGTGGGTTCGGAGCGCTGTTTGGCCTCAATAAAGATAAATATGAAGAGCCAGTGCTCGTATCGGGAACTGATGGTGTAGGCACGAAGCTTAAGATCGCGTTCGCTGCGGATCGCCATGACACGATTGGGATCGACGCTGTAGCTATGTGCGTGAACGACATTGTAGTGCAAGGTGCGGAGCCGCTATTTTTCCTAGATTATCTGGCTTGCGACAAAGTCGTACCGGAGAAAATCGAAGCGATCGTAGCAGGAATCGCAGAGGGCTGTCACCAAGCAGGTTGTGCGCTGATTGGCGGCGAAACGGCTGAAATGCCGGGCATGTATTCAGCGGGTGAGTATGATATCGCTGGATTCACAGTTGGCGTTGCTGACAAAGCGAAGCTGGTAACAGGCGCTAACATCGCTGCTGGAGACACAGTGATTGGTTTAGCTTCTAGCGGCGTGCACAGCAACGGCTTCTCACTTGTGCGTAAGCTTTTGCTTGAGGAAGATGGCTATGGCCTGAATGATGTGCTTCCGGAGCTTGGAGCTCCGCTTGTGGATGTACTTCTTGCACCAACTAAGATTTATGTGAAGCCTTTGCTGGCGCTGCTGGAGCAGCTTCCGGTGAAAGGGATGGCACATATTACGGGTGGCGGATTCATCGAGAATATCCCGCGCGTATTGCCTGACGGTGTAGATGTGGAGATTAATTACGGATCGTGGCCGATTCTGCCGATCTTCGGATTGATGCAGAACAAAGGAAACGTAAGCAACCGTGATATGTTTACTACTTTTAATATGGGAATTGGACTTGTTCTGGTAGTAAGTAGCGCTGATGGAGAACATGCTCTTGAACTGCTCAAAGCGAGCGGAGAAGAGGCTTTTATCATTGGTAAAGTGACAGAAGGGGAACGCAAAGTAACCTTTACTGGAGCTGAAGTGTGATGCAATGGAGTCGAATCGCTGTTTTGGCTTCTGGGCAAGGCAGTAATTTTGCTGCACTGATCGATGCACAGAGAGCAGGCTTGCTTGGTGAGGGCAATATTGAGTTGCTTGTATCCGACAAGCCAGAGGCACCTGTAGCTAAGCGAGCGGAGGATGCGGGCATTCCCACCCTCTTGCTGCGGCCAAAAGACTTCGCCAGCCGTGAACTCTACGAAGCAGAGATTGTAGCAGAGCTTCAGCGGCGGGAAATCGGGCTGGTTGTGCTGGCAGGATACATGCGTCTTATTACGCCAGTGCTTTTAACGCCGTATGCTGGACGAATTATTAACATTCATCCATCGCTGCTGCCTGCTTTTGCAGGAAAAGATGCAATCGGACAAGCGCTGGATTATGGCGTGAAGCTGACGGGTGTTACTGTGCATTTTGTCGATGGAGGTATGGATACCGGGCCTGTTATTGCTCAGCGCAGCGTAGCCCTGCAGGATAACGACACGGCGGATTCATTGGCAGAACGTATTCATAAGGTTGAGTATGAGCTGTATCCCGAAGTGGTTGGCGCTTTTGCCAGCGGGAAAGTGGAACTGAGTGGAAGAAAGACGATTATCCGCGAAAAGTAAGCTGCACCGCAGCCATTCGAAGTTTTGGATCGACATTTGGTGACAGACCGAGATGTTTCAGGGTATTTCTCGGGAAATATTGCATAAGCGGCGTTATGTGTCGCGTTGTGGGTTTTCTTCATATTAAATCGCACGTACAACCTGAAGGAGGACTATTCAAAGTGAGTATCAAAAGAGCGCTAGTCAGCGTATCGGATAAACAAGGTATCGTGGATTTTTGCCGCGAGTTGTCTGCATTAGGCGTAGAAATTATCTCTACAGGTGGAACAAGCACGCTTTTGGCTAAAGAAGGTGTTCCAGTTATCGGGATTTCCGATGTGACAGGATTCCCAGAAATCATGGACGGACGTGTCAAAACCTTGCACCCTGCTGTACACAGTGGATTGCTTGCGGTTCGTGATAACGAGGAACACACGCGTCAAATGAAGGAGCTTGGTCTGGACTACATCGATCTGGTTGTTGTGAATTTGTATCCGTTCGTGGAAACTATCGCAAAACCTGACGTATCCTACGAGGAAGCCATCGAGAATATCGATATCGGCGGACCTACGATGCTGCGTTCTGCGGCGAAGAACCATGCTTTTGTCAGTGTAGTGGTGGATGCTAATGACTACGCTACTGTACTTGAAGAGGTTCGCGCAGGTGGAGATACAACGCTAGAAACACGCAAACGTCTTGCGGCAAAAGTGTTCCGTCATACGGCGGCTTACGATGCCTTGATTTCCGATTATTTGGCTAACGTTACTGGCGAGCCTCTGCCAGAGCGCTACACCGTGACTTATGAGAAAATTCAGGATCTGCGTTATGGCGAGAATCCGCATCAAAAAGCAGCGTTCTATCGCAAGCCATTGGCGGCACTGGATACACTCACTGCGGCTGAACAATTGCACGGCAAAGAGTTGTCTTATAACAATATCAACGATGCTAACGCAGCACTGCAAATCGTGAAAGAATTTGAAGAGCCTGCTGTCGTAGCGGTTAAACATATGAACCCTTGTGGTGTAGGCGTGGGTGAAAGTGTATACGAAGCTTATCAAAAAGCTTACAACGCGGATCCAACTTCTATCTTTGGTGGGATTGTAGCAGCAAACCGCATTATTGATGCAGACACAGCGAACCTGCTGAAAGATATTTTCCTCGAAATCGTGTTGGCACCAGGCTTTACGGAAGAAGCACTGGAAATCCTTACGAAGAAAAAGAATCTCCGTTTGCTCAAAATCGGTAACCTTAGTACGGCTAGTGCGCGTAAGAGCAGCTTTGTAGTTACCTCTATTGATGGAGGAATGGTTGTACAGGAGAGCGATGTGCACTCTGTGAACCCAGATGATCTACAAGTCGTTACGGACCGTAAACCAACCGAGGAAGAATTGAAACAATTGTTGTTCGGATGGAAAGTAGTTAAGCATGTGAAATCTAATGCGATTGTGCTGGCTGCTGATGATATGACCGTTGGCGTAGGTGCAGGACAGATGAACCGCGTTGGTGCAGCTAAAATTGCAATCGAACAAGCTGGTGAAAAATCTAAGGGAGCCGTACTCGCTTCCGACGCGTTCTTCCCAATGGGCGATACGCTTGAAATGGCAGCAAAAGCAGGAATCACTGCAGTGATTCAGCCAGGCGGCTCCATTAAAGACGAAGAGTCAATTAAGGTCGCTAATGAGTATGGTATTGCTATGGTCTTCACAGGCGTCCGTCATTTCAAACACTAG

Protein sequences of DBSCAN-SWA_2

>NZ_CP009279|730250:741713|732882_733128_+|WP_036680912.1|DBSCAN-SWA
MLKATVYVTIKKSVLDPQGVAVQGALHSVGFQEVESLRIGKYMELTLDTDNRAEAEVRLKEMCEKLLANTVIEDYRYELED
>NZ_CP009279|730250:741713|733133_733823_+|WP_042124034.1|DBSCAN-SWA
MKFAVLVFPGSNCDIDCYKAVEDSLGEPVDYVWHTATDLSAYDCILVPGGFSYGDYLRCGAISRFAPVMAEVAKAAEQGKFVLGICNGFQILTEAGLLPGALRRNMSMKFRCHDTVLKVVNNETPFTIDYAKDEEIIIPIAHGEGNYYCDEETLAELKANNQIVFTYSDNPNGSVADIAGVSNVQGNVVGMMPHPERAANSLLGSEDGKRMFTSILKTWRDRHDAASIR
>NZ_CP009279|730250:741713|739386_740004_+|WP_042184753.1|DBSCAN-SWA
MQWSRIAVLASGQGSNFAALIDAQRAGLLGEGNIELLVSDKPEAPVAKRAEDAGIPTLLLRPKDFASRELYEAEIVAELQRREIGLVVLAGYMRLITPVLLTPYAGRIINIHPSLLPAFAGKDAIGQALDYGVKLTGVTVHFVDGGMDTGPVIAQRSVALQDNDTADSLAERIHKVEYELYPEVVGAFASGKVELSGRKTIIREK
>NZ_CP009279|730250:741713|740165_741713_+|WP_042184755.1|DBSCAN-SWA
MSIKRALVSVSDKQGIVDFCRELSALGVEIISTGGTSTLLAKEGVPVIGISDVTGFPEIMDGRVKTLHPAVHSGLLAVRDNEEHTRQMKELGLDYIDLVVVNLYPFVETIAKPDVSYEEAIENIDIGGPTMLRSAAKNHAFVSVVVDANDYATVLEEVRAGGDTTLETRKRLAAKVFRHTAAYDALISDYLANVTGEPLPERYTVTYEKIQDLRYGENPHQKAAFYRKPLAALDTLTAAEQLHGKELSYNNINDANAALQIVKEFEEPAVVAVKHMNPCGVGVGESVYEAYQKAYNADPTSIFGGIVAANRIIDADTANLLKDIFLEIVLAPGFTEEALEILTKKKNLRLLKIGNLSTASARKSSFVVTSIDGGMVVQESDVHSVNPDDLQVVTDRKPTEEELKQLLFGWKVVKHVKSNAIVLAADDMTVGVGAGQMNRVGAAKIAIEQAGEKSKGAVLASDAFFPMGDTLEMAAKAGITAVIQPGGSIKDEESIKVANEYGIAMVFTGVRHFKH
>NZ_CP009279|730250:741713|733800_736047_+|WP_042184745.1|DBSCAN-SWA
MTQQVSVKEPTAEQIAEQKIYSQFGVSDSEYELIKSFMGRLPNYTEIGVFSVMWSEHCAYKNSKPLLKRFPVTGPRVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPFQGAATGVGGIIRDIFSMGSRPIALLNSLRFGKLESDRVKYLFEHVVSGIAGYGNCIGIPTVGGEIMFDDSYDGNPLVNAMCVGLIDHDKIQRGVAKGVGNPVFYVGPPTGRDGIHGATFASVELSEESEAKRTAVQVGDPFMEKLVMESCLELIDSGIVIGIQDMGAAGLTCSSAEMASKAGNGLELYLDQVPQREDGMTPYEMMLSESQERMLFVVEPKDEAQAQEIFDRWGVICCKVGKVTDDGRLKLYHHGEVVGDMPVTALVDECPVYNKPSEVPAYYVENESVDTLRYAEVTDLGSALRTVLGSPTVASKAWVYNQYDYMVRTSTAVRPGSDAAVVTIHGTRKGLAMTTDCNGRYVYLDPEVGGRIAVSEAARNIVCSGAEPLAITDNLNFGNPEKPDVFWQMERAVDGMAEACRVLDTPVIGGNVSLYNENTTGSIYPTPVVGMVGLVTDTDHITTQGFKQEGDSILLLGVTKAELGGSEFQYAVHGVTEGRPPALDLATEKTLLSTVLTSIRGGLVRSAHDLSEGGLAVALAESCISGGIGANVELSANGLRSDIALFSESQSRIVLTAAPERAEELKAAIAASGVPVEIIGTVGGDRLRVNLDGASVLDEAVAELKFVWEDAIPCLMK
>NZ_CP009279|730250:741713|738346_739387_+|WP_042184751.1|DBSCAN-SWA
MSEAYKNAGVDIAAGNEAVERMKKHVKRTYRPEVMTDLGGFGALFGLNKDKYEEPVLVSGTDGVGTKLKIAFAADRHDTIGIDAVAMCVNDIVVQGAEPLFFLDYLACDKVVPEKIEAIVAGIAEGCHQAGCALIGGETAEMPGMYSAGEYDIAGFTVGVADKAKLVTGANIAAGDTVIGLASSGVHSNGFSLVRKLLLEEDGYGLNDVLPELGAPLVDVLLAPTKIYVKPLLALLEQLPVKGMAHITGGGFIENIPRVLPDGVDVEINYGSWPILPIFGLMQNKGNVSNRDMFTTFNMGIGLVLVVSSADGEHALELLKASGEEAFIIGKVTEGERKVTFTGAEV
>NZ_CP009279|730250:741713|730250_731546_+|WP_042184741.1|DBSCAN-SWA
MIERYSRPEMRAIWTEENKFKAWLEVEICACEAWAELGVIPHEDAAKLRKDAKFDIARIDEIEQETRHDVIAFTRAVSESLGAERKWVHYGLTSTDVVDTALGYLLRQANEILEKDIINFIEILKDKAIAYKDTPMMGRTHGVHAEPTTFGLKMALWYEEMKRNLERFRHAANGVQFGKISGAVGTYANIDPFVEEFVCRKLGTSPAPISTQTLQRDRHAEFMAALALVATSLDKFATEIRALQKSEIREVEEAFAKGQKGSSAMPHKRNPIGCENISGLSRVIRGHMVTAYENVPLWHERDISHSSVERIILPDATMLLNYMLNRFGNIVKNLTVFPENMKRNMNRTFGVPFSGRILTKLIDKGLSREQAYDTVQPRAMQAWEEQKQFRDIVEATPEITNVLTPEEIEDAFNPSWHLKHVDTIFRKLELL
>NZ_CP009279|730250:741713|737619_738039_+|WP_042184749.1|DBSCAN-SWA
MLRRLGYECSLCPCVLRTDGTRFTALRPPAAYRRREWLAKLVASLAKVGARLRPKRQEQLTKLVPVCCANAGLACLAKVGARLRPKRQEQLAKLVPVCCANAEPASLAKVGARLRPKRQEQLTKLVPVCCANAGPACFA
>NZ_CP009279|730250:741713|731864_732755_+|WP_042184743.1|DBSCAN-SWA
MTSSAVSTAVELINAPLLYKGKVRELYDLGENVLIVVTDRISAFDYVLDPAVPEKGNVLNRLSAFWFGKTKELMENHVVHIDVDLLGDIVKDKEALRNRVMVVHKAERIDIECVVRGCITGGGWRQYQETGKVNGIELPKNLRKNALLAQPIFTPAAKNDVGHDEDIPFEKMQELIGADLALELQEKSLQLFSFAREYCAERGIILADCKFEFGLLDGRVILIDEIFTPDASRFWAKDKYVLDIEIDSMDKEPVRTYLSASSWDKNSKPDPLPLEVVEETTRRYLDIYHRLTGKSL
>NZ_CP009279|730250:741713|736031_737528_+|WP_042184747.1|DBSCAN-SWA
MSYEIKTGKEQETPILWTGDFYNEGTGSGDIFDTLKEECGVFGVFGHPEAASMSYYGLHALQHRGEESAGICVADGRDFNYHRGMGLVKEVFDKDKIASLVGDMSIGHVRYSTSGDSRLTNAQPLVFKYRDGDLAIATNGNIVNEPLIRKQLEQSGSIFQTTSDTEVLAHLIARSSKDFVEAAKDALKQLVGGFAFLLMTNDKLIVASDSHGLRPLVMGRIGDAYIFASESCALEVIGAQLVRDIEPGELLVLDKNGLLEDRFTEPKRKALCAMEYIYFSRPDSDMNGANLHTARKRMGSRMALEAFVDADLVTGVPDSSISAAIGFAEQTGIPYELGLIKNKYTGRTFIQPSQELREQGVKMKLSAVRSVVDGKRVVMIDDSIVRGTTSRRIVNLLREAGAAEVHVRITSPPFKNPCFYGIDTPDRRDLIASYKSIAEMCEEINADSLAFLSPEGLITSIGGHNKDDYKGGLCLSCFDNDYPTQVDFDGAEKDGCSC

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042184741.1|730250_731546_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	5.2e-23	27.3
WP_042184743.1|731864_732755_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	3.5e-39	33.1
WP_036680912.1|732882_733128_+	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	3.7e-07	36.7
WP_042124034.1|733133_733823_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_042184745.1|733800_736047_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	1.3e-167	42.5
WP_042184747.1|736031_737528_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	4.8e-49	32.6
WP_042184749.1|737619_738039_+	hypothetical protein	NA	NA	NA	NA
WP_042184751.1|738346_739387_+	phosphoribosylformylglycinamidine cyclo-ligase	A0A0E3F760	Synechococcus_phage	1.6e-67	44.8
WP_042184753.1|739386_740004_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	3.4e-25	37.0
WP_042184755.1|740165_741713_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	2.8e-76	52.0

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP009279|2101971:2112268|DBSCAN-SWA
GATGAAACCGTTTCGCGCTCGTCTTACGTTTATACTTATGGCCTTAATCGGTATTTCCATGATTGGCACTGGATTTACGATGGCTCATCTGTTTAAGAGCTCCCATATAGCTGCTCTCGAAGAGAACATGTCCCGGGAAATAAATCTACTCGCAGGTACATTGGAATTTGTAGATATGGACGCCTCCAATTCCATTCCGTATTACACGGAGCAGGCAGAGCATATCGCCAAGCTTCTGGATTCCCGGATTACTTTTATTAGTAAGTCAGGCAAAGTTTTAGGGGATTCAGAGAAAAATCCTCTGGAGATGGACAATCACGCCAATCGTGAAGAGGAGATTGTTGCGGCTAAAGAGGGGACTGGACGAGCCATTCGTTACAGCGAAACTTTAGATCGCGAGATGTTATATGTAGCCGAGCGGGTGACCTCAGATCATGGTTTTGACGGTTACATTCGGGTCTCTATGGGACTGGATGCAGTAACGGAAGGGCTTAACCGTGCTTGGATGATTATGGCTGGGGGGTTAGTTATTTTGTTCCTGGCAGCAACTATTGTCAGCTACAAAGTGGCATCGAGCATGACTTCACCGCTTGAACAAATCACGAGAGTCGCGCGGCGTATTACAGATCTTGATTATGATGCAAGAGTCCATTTGAAGCGTAAAGATGAGGTCGGGCAGCTGGCGACAGCAATAAATGCCATGGCTGACAGTCTTCAAGCTCAGCTTAAGACTATTCGTGATAATGAGGATCTGCTGCAAAGCGTACTGGACAATATGACTGGCGGCATCATAATGATCAATGCGGACGAAGAAATTGCCCTGCTGAACCGAGCCTCAGAGCGGATGCTGGATGTTAGCAACAGTGAAATGGCGGGTCATTCGTACAAGGAGCTAAAGCGTCATTATGAGTTAACACGTCTGCTTGAAGAAGGGGTATCGAATAAAGAACCGCTCCATGAAGAACGAAGTATTTACAATCCGAGAGAGCGGATTGTACGTATGGACGCAGTACCTATGATCCAGGACGGGACGTATAGAGGCATGCTCTTCCTGCTGCAGGAAGTAACAGAGATTCGTCGCCTGGAGCGGATGCGAAGTGAATTTGTCGCTAACGTATCCCATGAATTGAAGACGCCGGTTGCCGCTGTTAAAGGATTTGCCGAGACCTTGCTGGGTGGTGGGGTTAAGGATGAGAAGACAGCCCGTTCCTTCTTGCAAATTATTTATGATGAGAACGAACGCTTAAATCGATTGATTGGAGATATTCTGGAATTATCTAAAATCGAATCTAAACGTGTGCAGCTCGATTGCTCACCTGTTCATATCATTGAATTCTTTGATTCCGTGCTGGGAACCATTAGCAAAGTGGCTGAGAAGAAAAGTATTAGTCTTAACGTAGAGGTTCCTGAGGAGCTGTTCATTGAGGCCGATGAAGATAAACTACGTCAAATTTTTATGAATCTGCTCTCCAATGCGATTAATTACACGCATGAAGGGGGTAGCGTAAAAGTCTACGTTAAGAATATACTGAAGCCAGATGGTTCTGAGAATGTCCAATTTACCGTTACCGATACAGGGATGGGAATTCCCAAAAAGGATCTGCCGCGCATTTTCGAACGTTTTTATCGAGTGGATAAAGCAAGATCAAGAAGTTCCGGTGGAACGGGGCTGGGACTGTCTATTGTGAAGCACTTGATAGATCTGCACCATGGTGTGATTTCGGTTAAAAGTGATCTGGGGATCGGAAGTTCATTTATTATTGAGTTGCCGCTCTTGCAGGAAGAAAAGGTGGATTAGATTTTTGTAAATTCACCTTATCGATTTTACACCAAGTTAACATTGTGGTGATATGATTGTTTTGTTGTTGCTTTGTAAAAATCAAACTATATGGAAGACGGGGGAACCTATGGCTCAACGATTGCTTGTCATTGAAGACGAACCGACACTGGCCCGGCTGCTGTCCTATAACTTAACGCAGGAAGGTTACGAGGTAACAGTAGAGGATCATGGTACGGCAGGATATGATCGTGCGACGAGGGAACCTTTTGACTTGATCGTATTAGATCTGATGTTGCCAGGTATGAATGGCATTGACATCCTTGATAAATTGCGTGGACAAGGTATCCGTACACCTATTATTGTGTTGACCGCCAAAAATGCGGAAGAAGATGTTGTTAGAGGTCTGAAATCAGGTGCTGATGATTATATAACCAAACCATTCGGCGTCTCTGAACTGCTCGCTAGAGTAAGTGCTGTACTTCGGAGGATTTCTGGACTTGCTGAGGAAGCACCGACAGAAACACCTATCTCTGCTTCTACCATTATTTTAGGTCAATTAGAGATTTACCCTGAGAGATATGAAGTCTCCCTCGGTGGTCATAGTATTAACTTACGGCCTAAAGAGTTCGAAGTGCTATTATATTTGGCTCGTAAGCCAGGGGTTGTGTTGACGAGAGATGATCTCATGAATGCTGTATGGGGCTTTGATTATATTGGTGGGCAGCGTACGGTGGACGTGCATGTAAGTTCACTTCGTAAAAAGCTTGAGCTGGATCCAGAATCCGTTCATATCGATTCGATTCGAGGCGTAGGCTATAAATTAGTGGTTAATAAAAAAAGAGCTCCGGTCATTTAGAGTGACTGGAGTTCTATTTTTTCTATACTTTTCATAAATAAGAAATGCTCGGAGTACTAGTTGGCTTCTGGGGAAATACTGTGATGTGGACCCATTCATCTCACTGATTTTACATTGCGTTAACATTTCTCTCCAACTGTATTTACACTAAAAGCTTATCATGGAGATCGAAGATGATGAGAAGGAGACGTAAACACTAATGAAATCCATCATTGACATAGAGAATCTTGATCTCTACTATGAGTCGTTCCACGCACTGAAGAATGTGAATCTGCAAATCCCGGAGAAACAGGTTACCGCTTTTATTGGACCTTCCGGTTGCGGGAAATCCACGTTGCTTCGCACATTGAATCGTATGAATGATATGATTCCTGGCACACGTATAGAAGGAACTGTAAACATCGGTGGCAAAAATATTTATAGTGATGAGGTAGAGGTGGAAAGCCTGCGTAAGCAGGTCGGTATGGTGTTTCAACAGCCGAATCCTTTTCCTAAGTCGATTTACGACAATGTAGCTTACGGTCCCCGTTTACACGGCATCCGTTCCAAAAGTGAACTGGATGAGATCGTAGAAAAAAGCTTGCGTCACTCCGCCCTATGGGAGGAAGTGAAAGATTTTCTGAAGAAATCTGCCCTTAGCTTGTCTGGTGGACAGCAGCAGCGGCTTTGTATTGCTAGAGCGTTAGCGGTACAGCCTGATATTCTGCTAATGGATGAGGCAACCTCTGCGCTCGACCCTGTATCCACTCTCAAGATAGAAGAGCTTGTTCAGGAACTAAGAAGTGAGTATACCATTGTTATGGTAACTCATAACATGCATCAGGCCGCACGTGTATCCGGTCGAACCGTGTTTTTCTTAAATGGTGTAATTGTAGAGGCGGCGGACACAGAGGTGCTTTTCTCGAACCCTAAAGATTCCCGCACTGAAGATTATATTTCCGGACGTTTCGGCTGATCAGATTTAAAAGGGTGTTCGTCCCTGGAAATGGCAAGCTGACCATACGTTAATGAGGAGGATCGCTCTTATTATGATTCGCAGAAAAGAATTTGATAAAGACTTGGAAGAGCTGCGCAGTCTGCTGCAGCAGATGGGTGAGCATGTTAAGGATGCTCTTGAAGGTGCAATTAATGCATTACAAAATCTAGATACAACGCTCGCACAGGAAGTCGTTGAAGCGGATTTACAGCTGAATGCCATGGAAGATAAAATCATGGAAATTGGCTCACGCTTAATTATTACGCAGCAGCCCGTAGCTAAAGATTTGCGCCGCATTATCGTTGCCTTCAAAATATCAAGCGATTTGGAACGCATGGGGGATCTGGCGATTGATGTAGCTAAGGCGACCATGCGTCTTCAAGGCCAACAGCTGATTAAGCCCCTTGTAGACATTCCTCGTATGGCTGAAATCGTGACAATTATGATCGATGAGGCGATCCAGTCTTACCTGGATGAGAACACTGATCTGGCTTATAAAATGGCACAGGATGATGATCAGGTCGATCAATTGTATGGTGCGATGATCAATGAGTTGTATTCTTATATGGTAACAAAGCCGGAGACAGTATCCCAAGCTATGTTATTGACACTGGTAGGCCGATATATCGAACGGATTGGCGATCACGCTACTAACATTGGTGAAAGCGTAGTTTACCTGGTTACCGGTAGTCGTCCAGATTTGAATGAATAGTTTTGATTCAAAAGATGTTTGGTACTTGTCGTAACTGCGGAGAATGTTTGGACTTCCGGCCGCTGTTGTCTCCAGATTTCTTGATTTTATACCGCTTTTTATGGTTGAAATCCGGAGACAAAGGCGGGCGCTTCGCTCCTACAGTTCCAAACTTCTCCTCCATTACTATCGTACCTTCACATCTTTTGTGTTTTTAGGTAAATGAAAGTAGCCGTCCTTTTATAAGGGCGGCTACTTGTTGTATTCCCCCATATTAGCTCTTAATGTTACTAACATTTCAGCTAATCCCATTGTTTAAGTTGGTATAGCCGTTTCTACTTGGACAGGCCATATGTTAAGATGTAAGAAGTAAGCATGAAAAAGGCGAGGTGCACTATGGACAAGTTGATACTTATAGATGGAAATAATATTATTTACCGCGCATTTTTCGCGATGCCTCCGCTAACGAATACAGCAGGGCAACAGACGAACGCGGTGTACGGTTTCACAACGATGCTGCTCCGTTTAATTGAAGAACACAAGCCGACACATATGATTGTTGCCTTCGATGCAGGAAAAGTCACATTTCGGCATGAAGGTTATGAGGATTATAAAGGCGGTCGGCAAAAGACACCTCCCGAGCTCTCCGAGCAGTTTCCACTGCTGAAAGATTTGCTCAGAAATCTGGGTGTACCGCAGTTTGAAATTGGCAATTATGAGGCCGATGATATTATTGGAACCATTTCTCGCCAAGCAGATGAAGCAGGCCGGCAGGTTATGATCGTGTCGGGAGACAAGGATATGCTTCAATTGGCTTCCGAACATACGACCGTTGCGTTGATCCGCAAAGGAGTTACTGAGGTTGAGCTTTATGGACCAGAACAAATTCGTGAGAAATATGATTTAACACCCGAGCAGATCATCGACCTTAAGGGACTGATGGGTGATGCGAGTGATAACATTCCGGGCGTTCCGGGTGTTGGTGAGAAAACAGCGCTCAAGCTGTTGCATCAATTCGGATCGGTTGAAGGTGTATTAGCAGGAACCGGTGAGCTTAAAGGTAAAATGAAAGAAAAACTGGAAGCACACGCGGAAGACGCTGTCATGAGTAAGAAACTGGCAACCATCTATCGTGAAGTGCCTCTTGAGCATTCGTGGGAAGATATGATCTTTAATGGAATTTCTGCGGATACAGCAGGACCCGCACTCGCAAAATTAGAATTCAAATCACTTCTGGAAAGGTTGTCACTTAGTGCCTATGCTCCAGTAGCTGATGGAGAAGAGGGTGCAGCGGAAGTAGAAGCTGCTACACTCGATATTTCGATCGTGAGTGAAGATGAACTTGAGGCGCTAAATGAAGCGCTCCCTAGTATTTCGGCACTGCATGTAGAATCCAATGGGGATAATCCGCATCGTGCCGAGGTGATCGGGGTAGGGCTATCTACTCTGGAGCGACATTATTATGTGCCGTTTGAATTACTACAGAAACCAGCGGCTGCGAAGCTACGTGACTGGTTAGGAGATGAGAAGGCTCCGAAGAGCGGATATGATCTTCACCGTGCTGATTTGGCACTGCATTGGCAGGGGATTGCTTTTGCAGGTGCAGCCCATGATGTGCAGCTAGCGGCTTATTTGCTGGATCCCACGGAAGCTAATCAGAACCTAAACGATCTCGCTACGAAATACGGCTTGCCAAGATTGTCACCTGATGAAGATGTATTTGGTAAAGGCGCCAAATATAAGATTCCTGAGCTTGAAATCTTAGGAAATCACGTCGCACGTAAGAGTGCTGCGGTACTTGGCATCGCCCAGAAACAACAGCAGGAATTGATTGAAACGGCGATGACCGGACTGTTCGAGGATCTCGAAATGCCATTATCACGTATTCTTGCGGATATGGAGAAACAGGGGATTGCAGTCAACGAAGGGGATCTTAAAGAATTAGGAAAAGAATTCGAAGCTCAGATTTCAAAGCTGGTCACCGAAATTTATGAAATTTGTGGCACAGAGTTTAATTTGAATTCACCTAAGCAGTTGGGCGAGATCTTATTTGTAAAACTGGGTCTTCCTGTCGTCAAGAAGACGAAGACCGGATATTCAACAGACGCAGAGGTGCTGGAAAAGTTAGCACCGTATCACGATGTGGTACGTTTGATTCTACAATATCGCACGATTGCCAAATTGCAATCCACCTATGTAGAGGGGCTACTCAAGGAAATTTCCCCGAAAACAGGGAAGGTGCATACATTCTATCGGCAGACGATTGCTGCGACAGGACGGCTTAGCAGCCAATTTCCGAACCTGCAGAACATTCCAATCCGCTTAGAAGAAGGACGTAAAATCCGTAAAGTGTTTGTTCCATCCGAACCGGGCTGGTCCATTCTGGCGGCGGACTATTCGCAGATTGAACTACGGGTACTTGCGCACATCTCCGGTGATGAGCGGATGAAGGAAGCTTTTCTCCATGATATGGATATTCACACGAAGACAGCGATGGATGTATTTGGAGTTACCGCCGATCAGGTTGATAGCAATATGCGTCGTGCTGCTAAAGCCGTTAACTTTGGTATCGTGTACGGAATCAGTGATTATGGTCTGTCGCAGAACTTGAATATTCCTCGCAAAGAAGCCGCTCAATTTATTGAGCAGTATTTTGAGGTATACCAAGGTGTACGTCGATATATGGATGATATTGTAGTTGATGCAAGGAAACATGGTTATGTAACCACGCTGCTGGAACGCCGTCGTTACTTGCCTGAGATTAATGCGAAGAACTTTAATCTACGTTCTTTTGCGGAACGTACAGCAATGAACACACCTATACAAGGAACTGCCGCTGATATTATTAAGCTGGCGATGGTGCATATGGACAAGGCTCTATTTGAGCGTGGGCTAAAGAGCCGTATGTTGCTTCAGGTACATGATGAGCTTGTATTCGAGGTGCCAGAGGATGAAATGGAGCTTATGAAGACGCTTTTGCCGGAAGTAATGGGTGGAGCATTGCAGTTATCGGTGCCGCTTAAAGCAGAGGTAAGTTTTGGCAGCAACTGGTACGAAGCGAAATAGGCTCCCTTTAAGGTGTGCATATCAGCTATAATGTAGTTGAGGTGAAGACATCATGCCGGAATTACCGGAAGTAGAGACAGTCAAGAGAACACTGAATGATTTAGTCAATGGAAAGCAGATAGAGAGTGTAACCGTCCGGTTGGCCCGGATTATTCAGCGGCCGGATGATATTCAGGCTTTTGCCAACCTGCTCGCAGGTCATAGCATTGTTAATGTTGAACGAAGAGGGAAATTTTTGCGCATCGTGTTAGACGGTCTGGTGCTGGTATCTCATTTACGGATGGAGGGCCGTTACGGACTTTTTTCGAACGAAGATCCACTGGACAAGCATACGCATGTGATATTCCATTTTACCGATGGCACTGAGCTGCGTTACACGGATGTTCGTCAGTTTGGTACAATGCATCTTTTTCAGATTGGTGAAGACCTCCAACTGCCTCCTCTTAATAAGCTAGGACAGGAGCCGCTGGAGCCATCCTTTACGCCGGAGAGGTTTAAGCAGATTGTATCAGGCAAAAGCACAAAAATTAAATCGCTGCTGCTGAATCAGGAATATATCGTCGGCATAGGTAATATTTATGTAGATGAGTCGTTACATCGTGCAGGGATACATCCTGAAGTCAGCGCCAAAGACCTTTCGGACGAGCAACTTGATCAGCTGCATCACGCTATTGTCAGTACGCTGACGGAAGCGGTAAACGCTGGTGGTTCGTCTGTAAAATCATATGTGAATGGTCAAGGTGAGAGCGGCACTTATCAGCAGCAGCTGTTGATTTACGGTCGTAAAGATCAGCCGTGTAACCACTGTGGAACGATGATTGAGAAAACGGTTGTAGGTGGCCGCGGCACGCATTATTGTCCAAGCTGTCAGCGTAAGGTTGAAAACTGAAGAAGTAATTAGGTTGGCACCCACTACTTGTCCCGCCCATATACTGTGTGAAGAATGCTTAATAGAGAACGGAAGCTGAATGAAGTGTATTCTGCAGTGTTCCGGTTCTTCACAGGAGGGATTGCGGGTGCTCAGCCCATTTTTTTCACTAATATTACTAGCTTTTGCTTTGAGTTTGGATGGTTTTGGCGTTGGTATTACATATGGACTGCGTAAAATGAAAATACCATTGCTCTCCATTCTGATTATCTCGCTTTGTTCGGGGGTAGTTATCTGTGTATCTATGCAAGTGGGTGTTCTGCTTGCCAAGGTAGTGTCTCCACATGCAGCTTCTGAGGTTGGCGCTGTTATACTCGTGCTAATGGGGTGCTGGTCGCTCGTCCAGATGTTAATGCAGAAAGAGAAGGAACAGACAGGTGAGCGTAAAGTAGGTAGTGAAGAAAATGTGCTATCCACAGAAGCTCGGGCAGAGGTAGCTGTTGATACTGAAGATGTTGTAGAACAGGTTACCATGGCTCCTGAGCAGGCAAAGTCGGCTGTCTTTTCCCTTGAGTTACGACGATTGGGGATTGTTGTACAGATCTTACGTACTCCGTCTTCTGCAGATATGGATGATTCCGGGAGTATTTCTTCGATGGAGGCTATGCTGCTCGGGATTGCCCTCTCTCTAGATGCTTTTGGAGCTGGACTTGGCGCAGCATTGCTGGGGTTCGATCCGATATGGACATCACTTACAATTGCTCTGTTTAGTGGTACATTTCTATTGCTGGGCATGAAGACTGGATTAAGATTCGCCGGGAACTACTGGATGAAGCATGCTGCTGCACTACCCGCGTTATTATTAATTACAATGGGAATACTGAAGCTATTATGAGGTGAGTACATGATTATTGGCTTAACCGGAGGCATTGCATCCGGAAAAAGCACGGTGTCCGCACTGCTTGTGAGCAAGGGAGCGAGGCTGGTTGACGCGGATGTGATCGCCAGAGAAGTTATGCTCCCCGGTCATGAGGTGCTGGCTGCGGCTGTGAAACAATTCGGAAGCGAGATCCTCTCTTCGGATGGCACACTGAATAGGGGCAAGCTGGGGGACATTGTATTTCAAAACCCGGCGGCCCTGCAAGCCCTGAACAATCTGACGCATCCCGCAATCCGGCGGGAGATTAAAGAACGTATGAACAGCATGGAGGAAGAAGATCCAAAGAAGTTAACAATTGTGGATATCCCTCTTCTTTTCGAATCAGGACTCGAGAACATGTTCCATGAAATACTGGTGGTTTACGTGCCTCGTGAAGTGCAAATCGCTCGATTAATGGAACGTAACGGACTTTCTATAGAACAAGCAGAAGCACGCTTAAATGCACAGATGGATATTGAAGCGAAGCGTAACAAAGCGGACTATATCATTGACAACAGTGGCGAACTTGCGCACACTGAGCAACAGGTTGCTGTTCTTTGGGACAGGCTGGGCTTATCATGAAATGGTTACGTAAAAAAAGAGTCCTTCTTCTGTTATTCATTGGTTTTACTGCGATATTGTTTCTGAGTACGAACTGGATGTCCTGGTTTTATCCGATCCATTATAAAGATGAGATCCGTAAGCACAGCGTTACGTACGATATTGACCCATTTCTAGTGGCTTCGATTATCCGAGTGGAAACGAACTTCAAAACTGGACGAGAATCCAGAAAAGGTGCTATAGGTTTAATGCAGCTTATGCCGGATACCGCCAAATGGGCCCTTGAAAAGGCCAAGCTTCCTGATGTTTCTATGGAGGAGCTAAAGCATGAACCATCAGCAAATATTGAATTAGGTACCTGGTATCTTTCAACATTATCCCGTCAATTCGAAGGTAAACCTACAGCGGTTATCGCTGCATATAATGCTGGACCGGGTAAAGTTCAAAAATGGCTGGATGAGGGGATCTGGGATGGAACGGATGCTACGATTAAGGATATTCCGTTTGGTGAAACCCGCCATTATGTACAGCGCGTCAACTATTACTATGATCAGTACACGGATATTTACAACGAATTCTAA

Protein sequences of DBSCAN-SWA_3

>NZ_CP009279|2101971:2112268|2103877_2104606_+|WP_042125998.1|DBSCAN-SWA
MAQRLLVIEDEPTLARLLSYNLTQEGYEVTVEDHGTAGYDRATREPFDLIVLDLMLPGMNGIDILDKLRGQGIRTPIIVLTAKNAEEDVVRGLKSGADDYITKPFGVSELLARVSAVLRRISGLAEEAPTETPISASTIILGQLEIYPERYEVSLGGHSINLRPKEFEVLLYLARKPGVVLTRDDLMNAVWGFDYIGGQRTVDVHVSSLRKKLELDPESVHIDSIRGVGYKLVVNKKRAPVI
>NZ_CP009279|2101971:2112268|2109391_2110228_+|WP_042186551.1|DBSCAN-SWA
MPELPEVETVKRTLNDLVNGKQIESVTVRLARIIQRPDDIQAFANLLAGHSIVNVERRGKFLRIVLDGLVLVSHLRMEGRYGLFSNEDPLDKHTHVIFHFTDGTELRYTDVRQFGTMHLFQIGEDLQLPPLNKLGQEPLEPSFTPERFKQIVSGKSTKIKSLLLNQEYIVGIGNIYVDESLHRAGIHPEVSAKDLSDEQLDQLHHAIVSTLTEAVNAGGSSVKSYVNGQGESGTYQQQLLIYGRKDQPCNHCGTMIEKTVVGGRGTHYCPSCQRKVEN
>NZ_CP009279|2101971:2112268|2110355_2111102_+|WP_042186553.1|DBSCAN-SWA
MLSPFFSLILLAFALSLDGFGVGITYGLRKMKIPLLSILIISLCSGVVICVSMQVGVLLAKVVSPHAASEVGAVILVLMGCWSLVQMLMQKEKEQTGERKVGSEENVLSTEARAEVAVDTEDVVEQVTMAPEQAKSAVFSLELRRLGIVVQILRTPSSADMDDSGSISSMEAMLLGIALSLDAFGAGLGAALLGFDPIWTSLTIALFSGTFLLLGMKTGLRFAGNYWMKHAAALPALLLITMGILKLL
>NZ_CP009279|2101971:2112268|2111111_2111708_+|WP_042186560.1|DBSCAN-SWA
MIIGLTGGIASGKSTVSALLVSKGARLVDADVIAREVMLPGHEVLAAAVKQFGSEILSSDGTLNRGKLGDIVFQNPAALQALNNLTHPAIRREIKERMNSMEEEDPKKLTIVDIPLLFESGLENMFHEILVVYVPREVQIARLMERNGLSIEQAEARLNAQMDIEAKRNKADYIIDNSGELAHTEQQVAVLWDRLGLS
>NZ_CP009279|2101971:2112268|2111704_2112268_+|WP_042186562.1|DBSCAN-SWA
MKWLRKKRVLLLLFIGFTAILFLSTNWMSWFYPIHYKDEIRKHSVTYDIDPFLVASIIRVETNFKTGRESRKGAIGLMQLMPDTAKWALEKAKLPDVSMEELKHEPSANIELGTWYLSTLSRQFEGKPTAVIAAYNAGPGKVQKWLDEGIWDGTDATIKDIPFGETRHYVQRVNYYYDQYTDIYNEF
>NZ_CP009279|2101971:2112268|2106669_2109339_+|WP_042186549.1|DBSCAN-SWA
MDKLILIDGNNIIYRAFFAMPPLTNTAGQQTNAVYGFTTMLLRLIEEHKPTHMIVAFDAGKVTFRHEGYEDYKGGRQKTPPELSEQFPLLKDLLRNLGVPQFEIGNYEADDIIGTISRQADEAGRQVMIVSGDKDMLQLASEHTTVALIRKGVTEVELYGPEQIREKYDLTPEQIIDLKGLMGDASDNIPGVPGVGEKTALKLLHQFGSVEGVLAGTGELKGKMKEKLEAHAEDAVMSKKLATIYREVPLEHSWEDMIFNGISADTAGPALAKLEFKSLLERLSLSAYAPVADGEEGAAEVEAATLDISIVSEDELEALNEALPSISALHVESNGDNPHRAEVIGVGLSTLERHYYVPFELLQKPAAAKLRDWLGDEKAPKSGYDLHRADLALHWQGIAFAGAAHDVQLAAYLLDPTEANQNLNDLATKYGLPRLSPDEDVFGKGAKYKIPELEILGNHVARKSAAVLGIAQKQQQELIETAMTGLFEDLEMPLSRILADMEKQGIAVNEGDLKELGKEFEAQISKLVTEIYEICGTEFNLNSPKQLGEILFVKLGLPVVKKTKTGYSTDAEVLEKLAPYHDVVRLILQYRTIAKLQSTYVEGLLKEISPKTGKVHTFYRQTIAATGRLSSQFPNLQNIPIRLEEGRKIRKVFVPSEPGWSILAADYSQIELRVLAHISGDERMKEAFLHDMDIHTKTAMDVFGVTADQVDSNMRRAAKAVNFGIVYGISDYGLSQNLNIPRKEAAQFIEQYFEVYQGVRRYMDDIVVDARKHGYVTTLLERRRYLPEINAKNFNLRSFAERTAMNTPIQGTAADIIKLAMVHMDKALFERGLKSRMLLQVHDELVFEVPEDEMELMKTLLPEVMGGALQLSVPLKAEVSFGSNWYEAK
>NZ_CP009279|2101971:2112268|2101971_2103768_+|WP_042186539.1|DBSCAN-SWA
MKPFRARLTFILMALIGISMIGTGFTMAHLFKSSHIAALEENMSREINLLAGTLEFVDMDASNSIPYYTEQAEHIAKLLDSRITFISKSGKVLGDSEKNPLEMDNHANREEEIVAAKEGTGRAIRYSETLDREMLYVAERVTSDHGFDGYIRVSMGLDAVTEGLNRAWMIMAGGLVILFLAATIVSYKVASSMTSPLEQITRVARRITDLDYDARVHLKRKDEVGQLATAINAMADSLQAQLKTIRDNEDLLQSVLDNMTGGIIMINADEEIALLNRASERMLDVSNSEMAGHSYKELKRHYELTRLLEEGVSNKEPLHEERSIYNPRERIVRMDAVPMIQDGTYRGMLFLLQEVTEIRRLERMRSEFVANVSHELKTPVAAVKGFAETLLGGGVKDEKTARSFLQIIYDENERLNRLIGDILELSKIESKRVQLDCSPVHIIEFFDSVLGTISKVAEKKSISLNVEVPEELFIEADEDKLRQIFMNLLSNAINYTHEGGSVKVYVKNILKPDGSENVQFTVTDTGMGIPKKDLPRIFERFYRVDKARSRSSGGTGLGLSIVKHLIDLHHGVISVKSDLGIGSSFIIELPLLQEEKVD
>NZ_CP009279|2101971:2112268|2105634_2106294_+|WP_042186547.1|DBSCAN-SWA
MIRRKEFDKDLEELRSLLQQMGEHVKDALEGAINALQNLDTTLAQEVVEADLQLNAMEDKIMEIGSRLIITQQPVAKDLRRIIVAFKISSDLERMGDLAIDVAKATMRLQGQQLIKPLVDIPRMAEIVTIMIDEAIQSYLDENTDLAYKMAQDDDQVDQLYGAMINELYSYMVTKPETVSQAMLLTLVGRYIERIGDHATNIGESVVYLVTGSRPDLNE
>NZ_CP009279|2101971:2112268|2104805_2105561_+|WP_042186541.1|DBSCAN-SWA
MKSIIDIENLDLYYESFHALKNVNLQIPEKQVTAFIGPSGCGKSTLLRTLNRMNDMIPGTRIEGTVNIGGKNIYSDEVEVESLRKQVGMVFQQPNPFPKSIYDNVAYGPRLHGIRSKSELDEIVEKSLRHSALWEEVKDFLKKSALSLSGGQQQRLCIARALAVQPDILLMDEATSALDPVSTLKIEELVQELRSEYTIVMVTHNMHQAARVSGRTVFFLNGVIVEAADTEVLFSNPKDSRTEDYISGRFG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042186539.1|2101971_2103768_+	HAMP domain-containing protein	W8CYF6	Bacillus_phage	3.2e-39	32.6
WP_042125998.1|2103877_2104606_+	response regulator transcription factor	W8CYM9	Bacillus_phage	6.6e-36	33.9
WP_042186541.1|2104805_2105561_+	phosphate ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	2.1e-16	33.0
WP_042186547.1|2105634_2106294_+	phosphate signaling complex protein PhoU	NA	NA	NA	NA
WP_042186549.1|2106669_2109339_+	DNA polymerase I	S5M8J1	Bacillus_phage	5.6e-48	29.7
WP_042186551.1|2109391_2110228_+	DNA-formamidopyrimidine glycosylase	A0A127AWE5	Bacillus_phage	4.5e-20	29.8
WP_042186553.1|2110355_2111102_+	membrane protein	NA	NA	NA	NA
WP_042186560.1|2111111_2111708_+	dephospho-CoA kinase	NA	NA	NA	NA
WP_042186562.1|2111704_2112268_+	lytic transglycosylase domain-containing protein	A0A0H3V0Q1	Geobacillus_virus	7.7e-16	38.3

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_CP009279|3642319:3648967|DBSCAN-SWA
TTTACTTGCCACGCTTATTGTGCCAGATCAATGCATGCAGCTGTGGAAGGACACGTACTCTATTCATATCAGCGTCTACGATTACTTTATTAAACAACCATTCCAGCCTTCCCAAAAGTCGAGCAGAAATGTCGCCTTCTTCAGTGACATCATCATTCCCAGGCTGCAGAAAGAGCTGCACATTGGGATATCGCTGGTGAATGTCTTTTGCATAATCAAAATCCTTATCGTCAAACACTACGACCTTCAAGCTATGCATAGAACGACCCAGTTTCTCCATTTTACTCATGATGTTATCTAGAATTTCCCAATTCGTCGTCATTCCTGAGCTTGGGGGTTTAGGGCTAATTGTCAGCACATCCACGTCATTGAACCAATCCTGCCATTTACTCCCCTGAGTTTCTATTGCAGCTTGTATCCCTCGCTCATGTAGCAGGTTAATAAAAGAGCCCAGCCCATCACCAATCAAAGCAGGATTTCCGCCTGAAATCGTAACACAGTCGAAATTATCTCCAGCTATAGCTAAAAGTTCATTCATAATTTCCTCCGAGGTCATCATTCGAACCTTATCCTTAGCAGTACCATCCCAAGTAAAAGCAGAGTCACACCAGCCACAGCGATAATCACAGCCATAGGTGCGGACAAACATTGTCTTCACACCAATTACCGCACCTTCACCTTGAATGGTCGGACCGAACATTTCAATTACAGGAATCTTACTCACAGTCACAGCCTCCATACAAGCGGTAAGATGGTCCATCCTCAGGGATATCTTCAGCCAGCACTTCTGCCCAGGAGGTTGGTGTCTCCCATAGCTTTACAGCATACAAGGGCAGCCCTGCCTGCTTAAGCTTATAGGCAATATAACAGGACATATTTTCAACTGTGGTGCGGAAAGACAACAAAGCTACTTTGGAACCCGTATTCGTTAATGTCTCTAACACAGGTTCGTTTCCCATAGCGAGAAAAGCGTGATCTAGACGGTCTACAAGGCTTTGTTGCACAGTCGTCTTGATATCACTGAAGTCAATAACAAACCCTTCGTCTGAATGGCCTTCCGTAGCCTCTGGTTTGCCCTTAAGCACTACTTCGAGCTTATAAGTATGTCCATGCAGATTGCTACATTTCCCTTTGTGACCAATTAATTGATGCGCCGCATCAAACGTAAATATTTTGCAGACTGAAACCTCGTTAAGCATTAAGATCCGGCCTCCATTCTCTCCGCCTCATATTGCTCAAGACCACGCTGACGCAACAGACAGGCTGGACAAGTACCGCAGCCACTGCCAATAATACCGTTGTAACAGGTCAATGTGTGTTCGCGAACATAATCAAAATAACCCAGTTCATCGGCCATTTTCCACGTTTCTTTTTTATCCAGCCACATCAATGGAGTGTGTATCGCAAACTCATAGTCCATAGATAAATTCAGCGTAACATTCAATGATTTCACAAATACATCACGGCAGTCCGGATACCCGCTAAAGTCCGTTTGGCAGACACCAGTGACGATATGGGAGTAACCCAATTGTTTAGCTAATATTGCGGAAAAAGACAAAAATAACAGATTCCGTCCGTCAACAAATGTACTAGGAAGCTCATCACCTTCGCCAGCAACGATATCAATATCCTGGCGGGTTAGTGCATTTGGTGCCAGCTGATTAAGCAGCCCAAGATCAAGGATATGCTGTTTTACATTAAACTTAGCTGCTATTTCTGTAGCAACTTCGATTTCAGCCGCATGACGCTGATTATAATTAAAGGTAACTACCTGCACTTCCTCAAACTGCTTCAATGCCCAAACCAGGCAAGTGGTGCTATCTTGTCCGCCGCTAAATACGACGAGTGCTTTTTTGTTCATCTTAATCTCTCCTTATCAACTTGTTGGGATTAGCGGTTATCCACTTTTTCTGGATAGAGGTCGTGATTCATTAAGCGGTGCTCCGCCATCGCCTCATACTTCGTACCCGGTCTTCCATAGTTGCAATAAGGATCAATAGATATGCCTCCACGCGGAGTGAACTTGCCCCATACCTCAATGTATCGTGGGTCCATCAGTGAGATCAGATCATTCATAATAATGTTGACGCAGTCCTCATGAAAGTCACCGTGGTTACGGAAACTAAACAGATACAGCTTTAATGATTTAGATTCCACCATTTTCTGTTCAGGAATATACGAAATATACAGTGTGGCAAAATCCGGCTGACCAGTAACAGGACATAAGCTAGTAAACTCAGGGCAGTTGAATTTAACAAAATAATCACGCCCTGGATGCTTGTTATCAAACACCTCAAGAATAGCTGGATCATAACCAAACTTGTACTGCGTTCCCTGATTACCAAGTAAAGTGACTTCTTGCATTTCCTCTTTCAATCTTCCTTCTGACACGACAAAAAACCCCTCTCTTTTCCTTCGGCCTTGGCCGGTAATGGAAAGAAGAACGAGATTTCGAAAACTTTGCTCCACTAAGAAGAAACGGAAGCAACGTCCGGGTTAAGGACTGCATCCGCTTATAAGATTTAATATACTCTTAGTTTTTTATAGAGGGAGTTCGCGAACCTCTCCTGCACAATCCGTGCAGACTTCTTCTTCATGCATATTGCGTCTTGAACTATACCATGGTAATTTGCTTCTGACAAGTTCTACGCTTTGCCCGTCTTCTGAATCCAGAGCGAAAGCACCACAATCCACAAGAGCAAAAGCAGGCTTTCTAGGAGCAATACTCCTTCTCCATTTAGAATACTGTTCAAATTCTGGACGATTTCAATACTTGGCAGAATTACAAAGATCGGATAGGTCCACTCTGGAAGAGCGACGTACACAGAAGCTACTAAGAAAAAAACGACCATAAATGCGGAGCAAATGGCTGAACCATTTTTGGAGGAACTTACCTTTAAACCAATGATAATTCCAACTTGCACAAAGATAATTCCACCCAATAACATATACATTAAGGAAGGGAGTAAATCCATTGTCAAACCTTGATTTAGTACATAAACAATCAGCTGTGATAACAAAGAAAAAACAAGAACAGATCCAGCTTTCGCTGTAATAATCTGGCCTCTGCTTAGCGGAGTAATCAACAGCGCATCATAAGTCTTACTCTCCCGCTCCTCAATTAATCCTGGGCCGGTAATCATGATCCCAACCATCACTTGCGCAAATAATATCCATGTAGAAAAAAGCATGAAGTCCAAACCGCTCTTGTCCACTACAGTGATGATGATTTTAGCCATAAATATAGGCAAAATTATTAGAATTACAGTCGCAGGATTACGCAGTATATCCTTACTTTCATGTTTAAACAGCTTCCATATCTGATAACTCAACTTAGCTCACTTCCCGTCAGGGCAGCGAATACATCTGCCAGCGAAGCTTCTTTACTGTGCATACTTAGAATTTGATTCGTAGACATTAGCTGATAGATATGATCTTTAGTAGCTTCTTCTGCAATCGGCCAGGATTTCATAACCACTTTCCCATCCTGCTGATATTTAACTTCAATTTCTGGTTTACCATAAATGGTCTTAAGTCTATGCGGTTCATCGAGTGCCACCAAAGCACCAGCGTGCATGATGCCCACTCTATCGCTTAATGCCTCGGCTTCGTGCATATCATGCGTCGTTAAGACGATGGTTGTGCCTTCTTCTTGAATTCTCTTGACGTGATTACGTATGAGTGAAGCTGAATTTGGATCTAACCCACTTGTAGGCTCATCTAAAAACAACACTTGAGGCTTATGTAATAATGCTCTGGCGATTAGAACACGCTGCTTCCAGCCTTTGGATAAGCTGCTTACTTTAGCTTTTTCCTTATCTAACAGCTGGAGGGTTTCCATGACTTCATTCACTCGATTTCCTGCTACCCTATACAGATCAGCGAACAGCTCCAGATTATTTCGAATAGAACTACGCATGTATAGGTTCGGAAGCTCGAAAACAACACCAATTTGAGCATGGATTTCTTTTTTATGACATGAAATATTCATGCCATTAATTAAAATTTCTCCGCTTGTAGACTGAAGAAGCCCTGTCATCATTCGCATCGTTGTAGTCTTCCCTGCACCATTGGGACCTAGAAATCCAAAGACCTCACCTTTCTCCACCGTGAAAGTAATTCGATCAACTGCACACCTCTCCTGATAATATTTTGAGACCTCAGTTAGCTGAATCAATAACACTCCCCCCTTTTTAGAATAGTTAACTTTCTTCTATCCTTATTCTGGTTGTAGAGGATTATCTCTGTTGTTGCTATTCTGTAACATTCGCTATTCCTTAGTACCTTCCTTTGTTCAAATCTGCTCAGATGTGGCAAAAATAAGGATTCAAATCCTAAGAAAAGGGTAACTTAAACATAATAATCTTCGAGGTAAGGGTGGGATCATCTAATGGAACAAAGTATACAGAAACTTATGGACTGGATTAACAGTCATGTGAATGAAACTATTGTAATTGAAAAGAAAGAGCTTCGTGATCTGGATAAAATTCATTTTAATCTAGAGGCTGTTGAGTTTCGGAGTGCGGAGGATGTTATCGATGATTATCTTGGGAGTGCATTAATATTAAAAGGATTTGGCAGCACTTTAAACGCCGATGGTGAGCTAGTATCGCTACCACACTCCACCTATGACTTAGCTATTGACGGGCTTCGGATTGAGGACATAAGTGATCGCAAGGCGGAAATAACTACTGAAAGAGCTAAATATACCCTTTCAGTGGATTAAACCATATGTAATGACAGCAAAAGAGCCCACAGTAATCTGTGGGCTCTTTCTAATTAATAGTTACTCTTCTCCAATGATCTCCACTTCAGTTTCAAGCTCCACTCCGAATTTATCCTTCACAGTCGCTCTTACATGGTGAATTAGCCCAATGTAATCGCTGGCGGTTGCATTATCAGCATTCACAATAAATCCTGCATGCTTCTTGGATACCTCAGCACCACCGATTCTTGTTCCCTGTAAGCCACTCTCTTGAATTAACTGACCTGCAAACCGACCTGGAGGACGTTTAAAGACACTCCCACAGGAGGGATACTCAAGCGGTTGCTTGGATTCACGCAAGTAAGTAAGTTCATCCATTTTCGCCTTGATGGATAATGCATCTCCGGAAGTCAAAGCAAATTTCGCCTCAAGCACGATGTATTCACCGCTTGCGAACACGCTTTTTCTGTAACCCCATTGCAGTTCATCCCCTTGCAGAGTCACCAATTGCCCGCTCTTAGTTATAGCCAGCGCACTGTGCAATACATCTTTAACTTCTCCGCCATAAGCACCTGCGTTCATGTAAAGCGCTCCACCAACCGTTCCTGGAATGCCACAGGCGAACTCAAGACCCGTAAGCTCCATATCCAGTGCATATCTGGAAACATCAATAATCTTGGCTCCACACTCCGCATATAAGAGATTGTCTCGAATCCCCACATCCGTTAGTCCTGCTGTTTGCAGAACTATTCCGCGCACACCTCCATCACGGATAATCACATTGGAGCCGTTCCCAAGTACCGTAAGGTTTATCCCATTCTGTTCCGCATATGTAACGATCTTTTGAATTTCCTCATAAGTAGCTGGTGCTGCCAAAATATCAGCTTTACCGCCCATTTTGGTATACACGTGATCTTTTAAGTTCTCATGACTCTTCACAATCCCTGCAGTCATTAACTGCTCTAGGTCATTTTGAATTTTGTCAATATTCATGTTTCATGCTCCTTTAACCATGTATAAATGATGGTCCTTGATCTATTTTTAGTAGTAGTATCATGGATTTGTAGGCAACCACAACTGTAACAACGAACAGGCTCCCTTGTCAATGACGGGAGCCTGTTCGTGTATGATTTTCGATTATGATTACACAGCTTTGTAGGCCGCAAGCTCGTAAGGAAGACACAGCGGCACACCTGTACGTGGATCTGGAACAATATCTGCCTCAATTCCAAAAACTTCACGCAGTACATCTGGTGTCATAACTTCTGTAGGTGAGCCTTCACTAACCACAGTACCGGACTTAATAGCTACCATATGCTGCGCATAACGAGTAGCATGATTCAAGTCATGCACTACCATGATAATGGTACGGCCTTCTTCCTCATTCAGCTTTTGCAGAAGCTGTAGAACTTCAAGCTGGTGAGCCATATCTAGAAATGTTGTTGGTTCGTCCAGGAATAGAATGTCAGTTTCTTGCGCCAATGCCATAGCGATCCAAGCACGCTGACGTTGTCCTCCAGATAAGCGGTCAATCGGACGGTCATGGAAAGGCTCCATACCTGTAACAGTGATTGCGTTGGAGATAATGCTGCGATCCTCTGCTGTCATTGTGCCAAATCCTTTTTGATGCGGGAAGCGACCATAGCTGACAAGTTCAGAGACCGTTAGTCCGTCTGGAGCTGTTGGGTTTTGCGGTAAGATCGCAAGCTGACGAGCTACCTCTTTCGTTGAAAAGTTATGGATCGATTTACCGTCCAACATTACACTGCCGCTCTTAGGCTTCATGATCCGGGCCATTGTTTTAAGAATTGTAGATTTACCAGAACCGTTAGCGCCCACTAGTGCGGTTATTTTTCCCGTAGGGATAGTTAAGTTCAACCCTTTAACAATTGTAGCCTCTGCATACCCAATACTTAACTCTTCTGTGTTCAAACGTTCTGACAT

Protein sequences of DBSCAN-SWA_4

>NZ_CP009279|3642319:3648967|3648166_3648967_-|WP_042188632.1|DBSCAN-SWA
MSERLNTEELSIGYAEATIVKGLNLTIPTGKITALVGANGSGKSTILKTMARIMKPKSGSVMLDGKSIHNFSTKEVARQLAILPQNPTAPDGLTVSELVSYGRFPHQKGFGTMTAEDRSIISNAITVTGMEPFHDRPIDRLSGGQRQRAWIAMALAQETDILFLDEPTTFLDMAHQLEVLQLLQKLNEEEGRTIIMVVHDLNHATRYAQHMVAIKSGTVVSEGSPTEVMTPDVLREVFGIEADIVPDPRTGVPLCLPYELAAYKAV
>NZ_CP009279|3642319:3648967|3644208_3644709_-|WP_076298718.1|DBSCAN-SWA
MSEGRLKEEMQEVTLLGNQGTQYKFGYDPAILEVFDNKHPGRDYFVKFNCPEFTSLCPVTGQPDFATLYISYIPEQKMVESKSLKLYLFSFRNHGDFHEDCVNIIMNDLISLMDPRYIEVWGKFTPRGGISIDPYCNYGRPGTKYEAMAEHRLMNHDLYPEKVDNR
>NZ_CP009279|3642319:3648967|3643034_3643517_-|WP_042188620.1|DBSCAN-SWA
MLNEVSVCKIFTFDAAHQLIGHKGKCSNLHGHTYKLEVVLKGKPEATEGHSDEGFVIDFSDIKTTVQQSLVDRLDHAFLAMGNEPVLETLTNTGSKVALLSFRTTVENMSCYIAYKLKQAGLPLYAVKLWETPTSWAEVLAEDIPEDGPSYRLYGGCDCE
>NZ_CP009279|3642319:3648967|3642319_3643042_-|WP_042188618.1|DBSCAN-SWA
MSKIPVIEMFGPTIQGEGAVIGVKTMFVRTYGCDYRCGWCDSAFTWDGTAKDKVRMMTSEEIMNELLAIAGDNFDCVTISGGNPALIGDGLGSFINLLHERGIQAAIETQGSKWQDWFNDVDVLTISPKPPSSGMTTNWEILDNIMSKMEKLGRSMHSLKVVVFDDKDFDYAKDIHQRYPNVQLFLQPGNDDVTEEGDISARLLGRLEWLFNKVIVDADMNRVRVLPQLHALIWHNKRGK
>NZ_CP009279|3642319:3648967|3646708_3647044_+|WP_042188628.1|DBSCAN-SWA
MEQSIQKLMDWINSHVNETIVIEKKELRDLDKIHFNLEAVEFRSAEDVIDDYLGSALILKGFGSTLNADGELVSLPHSTYDLAIDGLRIEDISDRKAEITTERAKYTLSVD
>NZ_CP009279|3642319:3648967|3647104_3648016_-|WP_042188630.1|DBSCAN-SWA
MNIDKIQNDLEQLMTAGIVKSHENLKDHVYTKMGGKADILAAPATYEEIQKIVTYAEQNGINLTVLGNGSNVIIRDGGVRGIVLQTAGLTDVGIRDNLLYAECGAKIIDVSRYALDMELTGLEFACGIPGTVGGALYMNAGAYGGEVKDVLHSALAITKSGQLVTLQGDELQWGYRKSVFASGEYIVLEAKFALTSGDALSIKAKMDELTYLRESKQPLEYPSCGSVFKRPPGRFAGQLIQESGLQGTRIGGAEVSKKHAGFIVNADNATASDYIGLIHHVRATVKDKFGVELETEVEIIGEE
>NZ_CP009279|3642319:3648967|3643516_3644179_-|WP_042188622.1|DBSCAN-SWA
MNKKALVVFSGGQDSTTCLVWALKQFEEVQVVTFNYNQRHAAEIEVATEIAAKFNVKQHILDLGLLNQLAPNALTRQDIDIVAGEGDELPSTFVDGRNLLFLSFSAILAKQLGYSHIVTGVCQTDFSGYPDCRDVFVKSLNVTLNLSMDYEFAIHTPLMWLDKKETWKMADELGYFDYVREHTLTCYNGIIGSGCGTCPACLLRQRGLEQYEAERMEAGS
>NZ_CP009279|3642319:3648967|3645646_3646495_-|WP_042188626.1|DBSCAN-SWA
MIQLTEVSKYYQERCAVDRITFTVEKGEVFGFLGPNGAGKTTTMRMMTGLLQSTSGEILINGMNISCHKKEIHAQIGVVFELPNLYMRSSIRNNLELFADLYRVAGNRVNEVMETLQLLDKEKAKVSSLSKGWKQRVLIARALLHKPQVLFLDEPTSGLDPNSASLIRNHVKRIQEEGTTIVLTTHDMHEAEALSDRVGIMHAGALVALDEPHRLKTIYGKPEIEVKYQQDGKVVMKSWPIAEEATKDHIYQLMSTNQILSMHSKEASLADVFAALTGSELS
>NZ_CP009279|3642319:3648967|3644963_3645650_-|WP_042188624.1|DBSCAN-SWA
MSYQIWKLFKHESKDILRNPATVILIILPIFMAKIIITVVDKSGLDFMLFSTWILFAQVMVGIMITGPGLIEERESKTYDALLITPLSRGQIITAKAGSVLVFSLLSQLIVYVLNQGLTMDLLPSLMYMLLGGIIFVQVGIIIGLKVSSSKNGSAICSAFMVVFFLVASVYVALPEWTYPIFVILPSIEIVQNLNSILNGEGVLLLESLLLLLWIVVLSLWIQKTGKA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042188618.1|3642319_3643042_-	7-carboxy-7-deazaguanine synthase QueE	A0A1U9WRB6	Streptococcus_virus	4.1e-62	47.8
WP_042188620.1|3643034_3643517_-	6-carboxytetrahydropterin synthase	A0A1U9WRB3	Streptococcus_virus	2.0e-25	48.6
WP_042188622.1|3643516_3644179_-	7-cyano-7-deazaguanine synthase QueC	A0A2H4J8Q7	uncultured_Caudovirales_phage	4.2e-61	52.8
WP_076298718.1|3644208_3644709_-	NADPH-dependent 7-cyano-7-deazaguanine reductase QueF	E7DN65	Pneumococcus_phage	2.5e-50	67.9
WP_042188624.1|3644963_3645650_-	ABC transporter permease	NA	NA	NA	NA
WP_042188626.1|3645646_3646495_-	ABC transporter ATP-binding protein	A0A2H4PQG7	Staphylococcus_phage	1.0e-32	38.0
WP_042188628.1|3646708_3647044_+	hypothetical protein	NA	NA	NA	NA
WP_042188630.1|3647104_3648016_-	UDP-N-acetylmuramate dehydrogenase	NA	NA	NA	NA
WP_042188632.1|3648166_3648967_-	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	6.0e-14	33.9

Sequences of DBSCAN-SWA_5

Nucleotide sequences of DBSCAN-SWA_5

>NZ_CP009279|3665223:3692488|DBSCAN-SWA
ACTATGCCACCTCCCAATCAATATTAAAGATTTCAATTGCATCGAGCGGTTTTGCAGATAAAGAGAAGTAAGCATAATCCATATCACTTTTCTTCGTTGGATGTTCGGTAAATGTAAATTCTGAGCCAATCGCCTTTTGTTCAGCACGAGTCTTCAAATAACTAACGACTGCTGCGATAAACATCCCCCGACCATCCTTGTCATTGTCCAGCTTAGCCTTGTTTGTTTTGCCAGCAAAGTAGATGTCGTTCAAAATTTGGTCAATCGTCATGGAAACTCTAATCTTGCCGAAGTCCTCCCGTTCCCCTGCCCCAAGTGTGGTCAATGTGTTCACTGCCGACTCAATAATATAGTCGTAGCCGTCACGGGTAGCCATCAGCGTGCCTTCGGCCAACCCCTTCAAAACTTCACTATGGCTCCAGTCCACTAGCGCTTCAGTCATTGGTACCTTAACACCCGTAAATGATTTATTTGCAGGTGTTCCAGCGGCTAAACCAGCTACCCATGCCGCCCACTGCAAGGAAGTATAAGTCTTTCCGTTGGAATGTTCACCAGCCAAAGAGCAATTGATGATAAAACGAGCATTAGCAGCGCGGCTGCGGGTGTTGTGAGCTTCAATATCATCATCAGCCCCCGATGCTCCTGCAATGACCAGCTGTGCTAGCTTGCGAGCCTTGCTACGCCGATCTAGCAGCCATTGCTTAGCAGCAGCTTGTACCGCTGCGTCCGAGGAAGGTAGATAAACGACATCAAACACTAGACCATCAATGCGATTTAAGATGCCGCTCCAATTGGCTGCCGTGATCGCTGCAGTACCAGTAACTCCGCCAGCCAACTTTGTATAGGCAACATCAGCCAAAGCCGTTGAACCTGTGTCCTTAAAACGCACCATGTTAGACTTTTTCAGAGCATTGATAGCTTCAGTTTTATCAGCGACCAAGAAAGTCTCAGTATCGTAGATACCTTTCGTATCCCGAACGACAATTTCTTTCTTGGTAGCATCAACCAAGCTGGCACGGATGAGGTACTCGAAATCATTTCCGCGAGTGCCTGGATAACGGGCCTCAATGGTATAGCTGCTGGCTACTGCAACGGATGCTGCTACCTCACTGTCGTTGGTGACACGGTAACCGATAACGGTCGCCCCGTTCTCAGCTGCTAGCTCCAACTCATCTACCAACAATTCAGATTCTTTCAAACGCTCCGACTGATCCGCCATATCCACTGCTTTATTTGGCAATCCCCACTCTGCTTGATACGGTACCAAAACGCGACCAGATACCGATAGGACACGAGACTTCGCAACCGCCTGCAGCTCCACATATGCACCTGGTCTATTCCGTTGTATCGACATTCACTGTTTCCTCCTTTTTTGTCAGTCCCAAATAGGCTTTCACCTTTTGAATAACTTCCTGCTGAGACAGCAGGGTATCATCGTCACAATCAAAAAGAGCGCCTGCAATTTCAAAGCGTTCCCGCTTCAAAACCACTGCGCTCTCTATCCATTCCTGCTTACTCCGCTTGTTCAGGGTATCTGGAACAACATTAGTAGGCTGGCGAATCTGTTTTTTTAAGTTCATTCTTTAAGTTTTCCTCCCTTTCTGTTTCAAAAGAAAAACCGCCTTTCCTTAGGCGGTTACAGTTAGTGCTTAATCGACATTTCCTGTTGCTGGTTCTTGCTCTTCATTGATTGTACAATCATCTAACCAAGGTTCTATACTCCAAACAGACTTCCGGGCAGCGTATAACGTATTATTATCATTTGTGTAGATGAACATTTCTTCATACCCATCCTTATACACGTCAAATAAATGTGCTGGCAGAATGGCAGCATCAAATGCCCATACCTCATCTTTTTTGCTGCAAACTACAGCTTCCCAGGGTATTCCATCCGTAACTTCATTAGTGAAATATACTCCCGTTTGTTTAAATTCCTCCGAGAACTTACTCAACATCGACCATACTAATGATTTAATCTCATCTTTTAACTGTCCTGTTCTGTAATCAAGCTCAATCTCTTCTGTCCAAAACAGTAAACTAACTTCTAACCACGATTCTTCCAATTCGCTAATGGCCTTAGGTGTCCATCCCATTACATATGGGCGGATATGAAATGGGTGCTCATTATAATCAAAAATCTGAGATTCCGCATCACCACCTACGTACATAAAACCATTATCAGAGACTTCATATTCAAGTTCTGGCGAAAAGTACTTAGATTCAAGAGATAGTGATTTTAGTACATTTGAGAAGTGGAGAATAATTTCCTTAAAGTTTTTTTGGTCGCATTTGAGGTAGGTCTGAATTTGGGAGTATTCGGGCATCTGGTCACATCATTTCTCAATTTTTAATGATTCCAGTATACCCCATTTACTCAAGTCTAACTAACGAAATTTCTGTTATATTAACAAATAGAATCGAACGTTAATTTCAACTAGGTTCAATAAAAAAGTCATTGATCTTCTGGATCTGCCGCCCGTCATCTCTGATCATAAGTTTCGGAACGTGAGTCAGAAATGAATACCTAAACGTAACTTCCATCCGATCATTCTGCGGCCGAGTGCGTGGAGCCTCAATCACCATCATGATTCCAAAGCGCTTCGAAACCACACAGAACCGCCGTTGGCGGAGGTAAAGGAAGAAGGGTGATAAGTCTAGAGGAATGGGCTCTCCGTCTTCCTCTACCACACTACGGTCGATGTCGTAATGAAAGACTAACCCTACATCCTCAATGATTCGGTCTGCCCGCGGCGTGTGTGCTTTATCGGATACCAGATCCGTCTCGATAAACACGCTTGGACGATCAAACTGCCCTGCCAGCCAAAGGGAACGATCTCGAAGAATCGGCAGCTCCGGGTATATCCGCTGCACGAGTTCTGCCCAGGCTTTTAATCCGACATCCATCATGACAGCATCCTCCCCAGCTCCTTCTCCAGACGCTTCATAATTAATGCATTCATGCCACCTTCCAGCTGTTGAACAGCAATATCAAAGTAATGTCGACCAATGAACGATCGTGGCTTAGCCATAAATCCACCCTTTGCCCTGGGATCATAGACAAATGTACCATTCGTTGCCCAATAACCTGGGACAAAGTGAGCCTTGTGGATGGTATAACCGTCATTGAGATGACGTGCGTAAGGAACATTTGAACCGACTTCGATAGTAATAGAATTGCGGTCAATATCCCACTCCCAAATGTTATTCTCCTCTCCACGAGTAAAGGAGTTCCACATCAATCCAGTGTCAATCAGATCCTGTTTATCAATCTCATCGATGACCAGGTTCAAAAGTGTTTCGCCCACAGCCTCAGCAATGTTCTTAAGGATCTGACTAACCCCTTCGTCGCTCAGCTTCTTAAATTTCTTCGCAAGTCCGTCAAAATCATGCACGCTCACTACCTTTCACCTCGCAAGTCACCAACAGCTCGCGCCAGTAACGGCGCGGGTTAGAGTCAATCACCAGATACTTGCGTCCGAACAGCAATACTTCGTCACTGATTTGAACGTCCGCTGTCTTTGGAACCCCGATTGTCTTTTTCACAATGTATATGACAGGAGTGGAATCTGCCTTGGCATCAGTCTGCGTCTTAACAACGAAACCTTTCAGATCTGCGATCTTTCCTACCTTCCGATCGCTGAATAAGTTTTCCGCATCTTGTTGGCGGCCGACCCGGTATACGGCCAGCGGTGTATTCATGCGGTGATTCATAGCAAATAGGCCGTGATGTTCCCATCATCCGGCCCGGACTGCTGCTTCTTGACCCATAGGAAGAGGATAGAGTCCACATCAGCATTGCCCGTGGTCTTCCCTTCTACTGCCTGCCGGGTGTAGGTCCAGGCGCCCTCACTCTCAGCTGAGTAACCGCGGGCGACGGAAGCCAAGTATTCCTCACTATCCTGCAGAGCCAGTGACTCCGCAAGTTTCACCCAGGCCAACATGAGCTGCTTATCTGCCACCTCCGGAAAAGGAACAGGTAAGTACAGCTCAATCCGGGTCTGTGCATCATCAATGTACTGCTGAAGCTGAACGTCAGTTGCCTCTTGTACAGCACTAACGCGGCTACGTTTCTTAAGGAGTGTCGCTTCCAGCATTCGGCACACCGCCGCCTTCCAGCGCCTTTAGTTCATTGATAAGCTCGGGCTTCTTCATATCCGCAAAGCCTTCAATACCGGCTTTCTTCGCCTTGTCCTTCAGTTGGGGAACTGTCAGATCTTCCAGCGGAATGACCTTCTCAGCATTCACTTCAAAATCAGGATGCTCATGCAGTTTTTCCAGCACAACTGAATCTTCCACTAGTACCGGTTTAGCCGGCTCAAAACGAATACTATACAGCCGAAGTGAGGCGTTCTTGCCTCTGTAGGTCACGTATGGCATTAGAATTCCACCCCTTCCACGTAGGCCAAAGCTTGCGGCTCTTCGAAGATGGCATCAAAGTCGGAATGAATCGCATAGAAACGCTTATCAGTCCAGATTGCCTCCTTGCCCTCAGTCGTCTTCCGAATCTGCATGTCATAAGTATGGACCATCGCAAAGTTCGGCTGATATGGGAAGAGAATCGATCCTTCCGGCATACTCCAAACCTCTTCGACCTCGTAGGCGTTGACTTTCTTCGTGCCCCCCAAGATCTGCAACTGAATAGATGCGCTGGTGTCCTTCTCAGCCAACATTTGTAGTCGCTCGCTGAAAGTATTTGGATGCATAAAGTATTTAAATACCCCACCAGCACGATAACGGGTTGGTATCGCACGTTCGACCTCAAACAAAATCCCTGTTTTCTCTTTAGCCGAAAGTGTCTTCCAATCTAAGTAATGACCGGTGGTACGTGCCTTCTTCAACCAACCGTCATTTATGCACAAAAACTCATAATCCGGATCCGTGTTCGAAGTTGCCGTATCACCATTAAAACCGATGTCTTGCATATTCTCACCATAGTTGTTAGCCATAGCCCGCATGATAATATCCTCTGCGTTTTGTCCACGCACCCGCTGAGTTTGGCGAATAAATTCCTCGGTAATATCAAATGGAACAATTACCGGCTCCACTGAATAAGGGATCTGTGGAAAGGTCAAACCAGGCGTGTTGGAAGCCATAATATTCTCTTTTTTACTACGCATGTTACGGCCTCGTACACCCACCTTGTCAATGGTTCCTTTAGAACTCTTCCGATTCTCATGACGAATCCCTTTTAGGAAGCCATTTGCTTCGTACGCCATATCGGTGAAGGCTTCCACTTCCTCATAGTTCAAGGCGTTCTGGTCCATCGGTGTAACGATGGTTGATTTACGAATGCTCGTATTTGCGATATTACCGTTTGTTCTCATGATTTGCATTCCCCCTTTAATTTACAGAAAGCGTCCGAAACTTACGGCGCCTTCTGATTTGCTGATTTCTTCTTGCTCACCTTGCGCAGAAGCACCGCGACTGTTCTTCACCAGTTGTACATCTGCTGCCAGCGTCTGCATCTGCTCACTCAGCGGTGCTAGAGCTTTCGCAATGGCATCCGTTATTGCAGTCTCTTCTACGGTTGCAGCCGGAGTTACACCGCATGCGGGCTGGTCACCTTCGACACCTTCTTCTTTCTTCAGCTCCGCAATCTCTGACGTCAGGCCTTCTACCTGCTTGGCGATCGGAGCCAGTGCGGCTGTTACAGCCTTGGCAATATCTTCAGCTTTCAAATCGTCATCCTCCTCGGGCTCTTGCTCTACAGGAGCCGTTTTATTTTTAAGTTCGGTCAATGCAGCGATCGCATCATCGACGTGTTTCAGGTTGTTGGCGGAAATCTTCTTGCCAGCTTTGGCAATCTGCTCAGGCGGTGTACCGATGGCTTTGACGATATCTTCTTTGGTCAGCACATCCTGCGCAATATCTACAAAATCTTGAAGCGCCTCACGAATAGTATCCACATCGGTTTCCATCCCGCTGTTATAACTGTCCCAATTAAAAAGAACCGAGTTGAGGGCATCCTGCGCCGCCCAAAATTCTCGGTTCTTCCGGTTCTTATGGTATTTATCAGCGACCGCACCCTTTTCGATCAAGCCCAGCGCTTTAGCTATTCGGCTCAAGATTCCCTTGGATACCTCCTCTTCCTCCTCGATCTCTTCCCGCTTACCTACACCCCACATTAAAAAGCCAGTTATCTCGCCTTTCTTGATTGCCTCCCAAGTATCATTTTCAGTCACTTTTACAGCTGCCACCCAGGAGCCCTTCACGATCTCCTGCTCACCGAGTGTCATGTCGCAAGGAGCAATGTAAGACTCAATGACGAAGCCCTTGTCCGCTTCGAGATCGTGCTGCTTGTCGATGTTGTAGGTATGCTGCTTCTCCATGAAGAGATGAGCTGCCTTCTCGATCTCGACTTCATCCATTTGATCGTCATGTGCGTCTGCCACATCTGGCTGATACACCACACCTTTGACAATCCGCTTATCATCATCAATCTTAGCGATTTGAACCTGTTTCTGGATGGCGTTCTTCCCGGCAGACTTGATGATGGCAAACGGCACGCCGTTCGCTCCTTTATCTACCAGAGAGATATGCGTGATTTTAGCATCTTTCAGTTTATAGCTCATATTCTGTTCTCACCTCCTTTCAATAAAAAAGCAGCTATTATTAGATGACTCCTTGCAGAATTTGAATTGTAATGGCATCAAACTTCTAAAAAAATAATAGACTGACCCTAGAAATTGAAACAGCGACAGCAAAGGACGAGAAAATAATGTCCTAGACTGTCGCTGTTTCATTGAACTAACGTGTCCCGTTAGCTTAACCAACTGTAGTGTGGTTTCTACTGTTACATTGTCTTGATAAAGATTTATTGGTCTTTCCGCATCAGTTGAATACTCATCCATATGCATTTAATCTTTCGAGTTTTATGATTCCGCTATGAGCCCCTTTACCTTCGATTCAAAAACCAGTTCATACTGTTGCCGTTAGCGCAATGACTGCAACCAAACCACACGCGATCATGATACCACATATTGGAATTATTCTGCCCGTTAGTTGAGAAAAGGCTGCCATTCGGCAGCCTTGATACAGTAGAACTATAGTGTTGCGTTAGTGGAATATACAATCTCTGATGTTAAGTTGAGTCAACCCTATTTACTTTTATCGGTGGTCAATAACGATCGTTTAATCTTTTGGTTTTATTTCGATCAGCATCTCTAACTCAGGAATATACATTCTTTTCATCGTATCGTCTTCTTGCTTATAAATAGAAATATACGGCTTCACAATGACAGACTGAGGAACATCATCGAAGGGTCTAAATTCAGCATTCATAGAAAACACCTCCGTACCAGGAATCAGAGTTCCGGCTAAGCCCCCTGACTTTTCAACGATATTTCCAGATTGATCCTCGATCACATAATCAAAATAGCGTCCTTCGGTAAGCTTCTCTATTTCATCCGAGTTCTCGATATTAACCACTAGTTGTGTCATGATTGGTGTGAATTCCAGACTTTTAACAGTAAGTTTTACTCTATTCCAGGTCTTCTCGGCATGAGGAGGTGTAACCTTATATACTTCTGCGGTTTTCTCGACAGGTATCTCGAACTGGAACGGCATTTCCTCCATGCCATTAAGTAATAAAGTAAACCCTAGTTGAAACGTTTCCGGGAACGAATACATCTCACCAGTACCACTATCCACCTCGGAGTGGCTGACGCTAATAACTGCTGCGCCTTCGCTTGGATTCGATTCATCTATTTGGGTATGTCCGCCTGAGAGGATCATTGGAAAGTCTTTACCATCGATTTTGACAAACGCCTCATACTTAACCGGAACACTTCCTCCTTCATTGTTCTTCATATGTAACACGAACGAGACATTTGATCCCGTATATATGACCTTCTTTATGCTTAGAGTGAATTCATTATGCGTTATGCTGTAGCTGGTCTTCGAGAGTAACCCTCTTTGATCGGCAGTCTCAAGCCCCACATTACCCGTAAGTTTAAATAATCGATCCATGATAGGAATTCCCTTCAAAGTCTGGGCGATTGTAGTCGAGACGAATGCTGAACTGAACAAGCAGACGAATAGAATCGCTGCGGCGGCAGCTACCAATGTAACTTTGCGTTTATTACTTGCAGTCTTTTTTATCGGTTCTAGCTCAGCAAACGCCTCCATCAATTTCAACTCTACGATCTCTGGTATGATTTCAGGTTCTTCTGCACGAAGTTCCAACAATTTGTTTTTCAACTGAAAGTCATTCATGCCTCATGCTCCTTTCTTTCTGAATTGGACAACCATTCAAGTAATTGCTTACGGGCACGATACATTCTCGTTTTTACTGCTCCCTCTGTTAGATCTAAAATATTGGAAATCTGTTTCATCGTCATATCGTGAAAATAGTGTAAAATAACAACGATACGCAATGGTTCGTCTAGATCATTCACTAGTTCCCGGAGATCGATGTTCTCATACCCTGGTTCAATATACGTGATCCTCTTAATCTCATCAGCCTCTCCTTGCTTGTGCTGGTTCCCTAGTATCCGATTGCACTCATTGATCAGAATACGGAATATCCACGTCTGGAAATAATCCGGTTGTTGGAGGGAGTGCAATGCCTTGTACGCTTTAAGTACTGTTTCTTGAATAGCATCGCCGCAGTCCTCATCAGTATTCAATAGGGTTCGTGCCATACGATACATGGGCAACTTAATTTCGGTGATGAGACGTATAAATGCTTCATGATCGCCTTTTCTTGCCTTTTTTATATCTTGCTTATTGATCACATCGATGATTCTCCTTTGCCTTATTAATTATGATAACACCGTTCAATCAATTGTTAGATACGAATTATTGCCAAAAGGTTACAAACAATTTCGTTAATCTTTCAATATAACAAAAACTGATCGTATGGATCGTCGTTCCGTCTGAAATCCAACTTCTTAATAACTTCAGAAGTTGCATATCTTCAAAATTCCAACAATATTGAAGCGACACGCAGAAGTTACCACACGGATTAAATCTAAAAAGCCTTTTTATCAATCCTACACTATCAATGTGTATACATAATAAAGATAGATTGTACAAAGATAACTAAACTATCCTGCCAGTTAGCTTAATGATCATCATCAGTCTATTACTCTATTTACTCAGCCTTCTGTTCCTCATTCAAAATAATCCCCTCCACTTTTTTTGTAATTCATATTAACTAAAAGAAGAAGGTTAGTCAGGAAATCACCTTTTCATTTCAATACAGATTGCATCGTGCATCGACATTTGATAATTTCCTCGGCACGTCCAGATGGATCTCCGGGGAACATCAGCTTGCTTTTACCGACTTCATAAGGCTTATCCAACGGTTGCACCTGGCCGTTGGCCTTACGGTGTGTCTTCCGGGTGCGATCCCCCTTGGAAGACCTCCATTTCTTCCCAGTTACCACCTCGGACTGTTTCCAGCCCTCCAGCTTACCACCATTGGCAGCAGCCGTGCTCATTGTGCGAGAAACGGTAATGGCCCTTTCCATATTGAATGGGCCGGCATCACCTTTGGCGGCTGCTGCACTGATCTCACGTACCAGCAACGCCCGCTCAGAAGGGGTCTTTCCCTCCTTAATAGCTTTCTGAAAAGCCCGGGTCATGACATCCTTGCTGGTCCCGTTCATGTCAGGTACCAGCTTCTTGAGGTTCTTCGCAAAACGGGATGCAGCTTTGTTCTTGGTGGACCAGGTCTTGTCGTTGTTCAGCACTGTCAGCTCAGATTCACCTGCCAAGTGAAACAGCGGCGTGAAGGAATCATATACCGCCTGTTCAAACTGGACAGTGAACAAATCACCGGACTGTACGGACTGTATAACCTTGCCCAGTTCCCCGATATCAAGCAGCAGCTCCTCACTGAGTTCCAGAATCGCATCATGCAGCGCCTTCCCCTGAAGCTCAAGAATCTCAACAATCCGATTCTCTCCTTGCTTGTAGAGTTCTTCCAGCACCGCGCGCTCTGCATTGGTCAGTTCCAAGCTGTCTAGAAACTCAGTGTCGTCCGCTTTGGCGATGAGCTCCCAGCATTCCTTACACATGGCCAGTTACCTCATCATGGCTCTGGCGAAGCAGACGCTTAGCAATTGTGGATACCTGCTCCTGCAGATCATTCACATCGGAGTCAGGTTCTGGCACAGTTAATGCATGCTGACTATTAATCAGTTGAGCAATCGGTGTATCCAAATATTCATCAGTGTATTTTGACTCATCGACCGTTGTATCAAGTACCTCTTCAGCGATCGGGATTAAATCTCTGATCAACATAATACCGCGGTCTGCGATAAAGTCCAGCAGCGCCTTGCGGTCTTCCGGATCAATAATACGCGGTCCACGTAAAGTCGCCCGTACGCGGAAGATGCCCATGGCAGGGAATAGGCGTTTATTAAAGATCTCGTCCATGATCCACTTGCGGTACGGTTCAAAGACCTGTTCCTCTGCAAATCGCAGTGCAGCTTGCGCCGTTGCACGGTTGTAATCGGAACTCTGACCAACCAGGATTGGGGGCAATCGGAACGAGGATAGGATATCAGCTTTCTTGTCCTTCCCGTATTCCAAGAACAAGGCATCTTGCTGTAATAGATCATTCAGTTTGTCCAGCTTAATAGACACCTTTTCGACTTTCTCATCTAGCGGTCCACCAGTCTCTTCCCCGATGGCTTCCAGATAAAGAATGCCTCCTTGGGACTGCGAACCTTTTACATTCTTCAGCAGCTCCATCGATTGCTTGGTCAGTCGTCCGTTGGTCACCGTTAGCAGCATGGAAAGCATTCGGCCGTTACTGAAATAAGAAACATTGAGTTCCTCCGCCTCTCGACTACCAACCACTCCAGGTGCATTCCCAAACCAGCGCGGTTCACCATAAGGACCATCATTTCCTAACTTTAAGGGAATGATCTGGTTCCCTTGACCCTCGGTTCCAAACGGCCGAAACCATACCACAGACTGCCCTCTCTTCATGGCATACTTCCGGGCATAGATATCTTGGGAGAATTCCTCGATCTTCTTCGATGACCGGATCAGCCGCTTACGCTTGATCGTCACCTTATCTGTCTCCCGTTTACAACGAACGAATTTCGGATTGATTCGGTAGAGTGTCGGGAACTCACTGCCGGCAGGCCAGGCCACCTCAACATTTGCATTCCCGCTGCTCTCGATGTCCTCAATCAAGGAGCCGATAATCTCATCCGGCGTATCCTCAAGGTTACAGGTCTCCAAGAACTTATCAGCCTTGTTCCACTCCTCCTGCGCGGTCTGATCACTCTCACCAGGGAGGTACTCCAAAGCAATACCATATCCAGCAATGTTTCGCTTGTATGCCTCGATGCACTGCGGAATGATGTTACTGTTCTTGACCAACAGTTTGCAGGAGGCAGGGTCATTGCCTGGTGGAAACGGAAGCAGCCCGTGCTGATCGTATAGGTTTTCAAAGCTATCCGATAGCTGTGCACTCGAGGGGATATGCCTTTCCTCTGCTTTTGATATTTGAAACCACTGTGCCTCGCCACTCATGCCTTACACCCACCCCACATCATGATCAGATCGCTCCTCTCTCTCTTTTTTACGTTGCTTCACACGCTGCAACAGATAATCCGTATGGATACCGTATCGGCGTGCATCACAGGTATGGTCGTTTTGCTTAATAGGCTTGTCTTCGCCCCGTTCAGCAGCCTTTTCATCCCATACGTAAGACACCAACTCCTGAAGCGAATTGGTGTTATCAGCACAGATATAAAGTTCATTATTCTGAAATCGGTTAGATACCGTCTGAATACCATCTAGTACAGTATTCACAGCAGCTCGGATATTGTTAATACCGCGCTTCTTCAACTCAATAATAAAAGCCTTTGCTGATGGGTCGATGAAGATTGAATACTCATCACCATCAAGAAAGGCCTCAAGGTAATCCGCATATTCACCATTCGTTTTCTCACCCTTATGGCGGATATTGTGGTAATACTCATCCAGTTCATAATAGACATTCCCGTTGACCCCGTATTTTAGGAATGCTGTCGGGTTGTTAGCCCCATAGTCGATACAAATGAACTTTCGATCAAACTTGGACGGAAACCAGTCCCGCGGCTTTTTGTGAATCGCATCATTAAACTTGGAGAAGATTACCCCTTCAGCCATGACCCAAAGCCCTAAGATGTACCGCTGATAGAAGATCCCGCTGTACATGCGACGGTACCGCTCACGCACCCGCTCGGAAAGAGAGAGATTATCCTCCATTGTAAAATGTAGGTGCAGTGCGTGCTTCTTCTGCAACTGTTCCAGCCATTCCTTTTTGAACCAATGATAAGGTCCTGCGGGGTTGCAGTTGAACCAGAGCTTTGCACCATCTACGGAACAACGAGCAGTCGCTTGATCAACAAAAGACTTCGGCATGAGTGCCACTTCATCGAAGAACATCCCGGCCAGCGTTATCCCGGCGATTAGATCCTGAGAACTTTCATCGCGTCCACCAAATAAAAAGAACCGGTTGCTTATTAAGCCCCGGGTCACAGTCAAAACATTTTCAGATCTATTATCATGAACATGATACCCACGGCTGGCCAACATGCGTTTCAGTGGACCGACTACGTTACGCCGGAGCGCACCGATGGTCTTCCCTGACATGCCGAACTGTTCTCCTCGGAAGGTGTCCATCCCCCATGCTATAAAGGAGAATGACATGCAGACCGTCTTACCGGCGCGGACCGAACCATCACAGATGATTGCGTCTTTATCGTGGTGTGGGCTTTCAGGTGTCCACCATGTCAGCACTTTAAGCTGCTTATTCGAGAAAGGGGACCACTTGAACGCCGCTGGTTTGAGTTTAAGCTTCGCCATCGTCGCTCCACACCCCCGCTGCCATGCCTTTCAGCGCATCGATAAAACCATCATCCTCAAAGGCTTCCTTACCTCCACCACCGCGCAACATTTGCAGCTCATACTCCATGGTTTCTATGCGGATACGCTTCTCGTCGTCGATCAATCGATTTTTGAGTTCAATGGCCCGAATCTTCTTATCCTGGATGCGGGTCAAGGCCTCCTCCAGCTTTACGATGTCGTCTATCTTGCGGAAACCCTTCTCCTCAATCTTCGACTCCATCATTTCATTTCGACTGTGTGGGATCTTCTTCGTAATGCCGGTCTTCTCATCATAGATCTCCGCGACTTCCTTGATGGCCTTCATCTCGTAGAGCACACTGCGCTCGGTCTCGGATAACCCATCCATCAGGGATTTGATCCGGTGCATCATGCGGCGCTCACGGATCGCTAGGAGGTAAAGAGACTCATTCGCTTGATTGATCGGGTCAGTGTCCACCTGATCAATGAGCTGCTGCTCCGTTTCGGTCAGGGTATCCAACCAGATAGTTTCATGCTCACCAGTAGTAACGGCCTTTTTATTACCGACTGGCCCGCCAGCACCACCGCTGTTTCCCTTGGCGTTTTTATTGCCAGTGGGAGCCCCGCCTCGATTACCGACTGCGTTTCTGTTCCCTTTGGGAGCACCGCGATTTGGAACGTTCCCTTTCATTTCAACTGGAACGCTCCCTTTAGATTCAGGTGGAACGTTCCCTTTGAGTTCCTCTTCCCAATGGTCAATTGACTTCCATTTACGCACCTTATTTTCGCCAACAAAAAGAGCGGCGGCGATGTCCTTAAGCTTCATCGTCCCGCCGTTCTCGAGCCACATCTGCTTTGCCTTATCCCGTTCGGGACTACGTTCTCTAGCCATGCTACATGTCACCACCCCCGATAAAAATTTGTTTACCTTAAAGGGTTCAGTCTATTTTCATAGAAATAAACTATACTTTGATAAAATTGTGTTAGGAGATTTAGAAATGAGCGAATATTATCCACCAATGCATTTAAAAGAATCCTTTCATTGCATATTTTGCAACGTATACACTACTCATGAATGGATTAGAACTTACCGTCAAGTCCCAATGGGATATAGTCAACTATCTGAACTCTATGTCTGTATGTGCAAACATTGCAATAAAAAATCTTATTGGCATGATGAAAAAATGATTTTACCCTCATCTGCCGGTGCTCCTAATCCTCATGAAGACATGCCAGTTGTGTTGATAGATGACTACTTGGAAGCTAAAGGAATTGTTAATCTTTCCCCAAGGGGCTCTACAGCACTTTTAAGACTTGTTTTGCAAAAGCTGATGATTGAGCTCGGAGAATCAGGAAAAGACATCAATAAAGATATTGGATCTCTAGTTAATAAAGGTCTCCCTGAAGAAATCCAACAGGCTCTGGACATTGTCCGTGTTATCGGTAATGAGTCTGTTCATCCCGGCGAACTTGATCTTCGGGATGATCTAGAAACTGCTTTACAACTCTTTGAACTAATCAATTTTATTATTGAAGAACGTATTTCACGCAAAAAGCGGATTTCTTCACTCTTTTCCCGTTTACCTGAGGCAAAACTGAAAGGTATTGAAGTTCGTGATAAGGACAAGCCAGTAACCACCTAAAGCTCATCCTTCTGTAACTCAATATCTATCTCAATCAGCTTCTTCAGGTCGTCCACCGTCTTGATTTCAATTCGACCATCCTGGAAGTCCTTGACCCATTTAGCTATGCCGGCTTTAATAATTTTACGATACTGCGCCTTGCTCTCCAGGATACCGGCCATAACTTCAAGCTCATGCTGCAATAAAATTTCATCTTGTGTTCCCATTTACGTACCCCTCGACTTTCCGTTATGATGGAATGCGAGACAGCGGATGTCTGAGAATGCCACGCGTGGCGCGCCGCTGTCTCAGCCGGGGGATACCCTGGGTGATGGGGAGGACGTTAACGCGTCCTCCTTTTATTTTGGGCAAAAGAAAACCACCTAGTATAAAGAGGTGGTTAGAAAGCAATTGCAGCAGTTATCAAATTCCAAATAACTCTTTCAGCATCTGACTCAGCTTTTTAAAATAAGCTTGATAGTGATCTTCTTTTGTTGTATTTGTAACATCAACTGATGATGTCACTGTTTTTTGTAAAGGACCCGAAACACCCATCGCCAAATGGCGATTTGCCAATGTATAGGCGATATTTAAAACTAGATCCAATCTTGAAAACCATACACTTGTTCCATACTTAGGTCCATCAGGATACCCAGCGATTAAAGGTGCTAACGAAAAACTCCCTGTTTCAGTAAAGGCATTTGCAGGTAATGCAGCCGCCATACATAACCATTTTGAGAAGATTTTATTATTTCTGTTCTCACTCAATAACTTTTGAGAAGCGGAAGCAAGAGTAAAACATCCTAATGAATGTGTAACAGCAAAACCAAGAGCAGTAGGTACTTCTTGTTTAATTCTCTTTAGGAAGGGGAAGATATAATCGCCTGTCAATGAAGCACGTCTTTCCAATTCTCTCCAAAATACACCGAGAACTAAAGGTTCCAAATCTCCTCCTGGTATCATTCCTAATAATAATTCGATAGCTGCTCGAATTATTGAATCACTTTCATCAGTTAACTCTGTATCATAACTTACAAGATAAATATCATGATCTGCATAACGACTATCGCTAAATACATCAACATGATCTTCAAAGTCCCTATAAAAAGAATAGGCATCGTCAAGCGAAGCATTATAACCCATTCCATGAACCAAAATACTTGGATACTTATTCTTTGGAAAGACATGGCTTGCAATATCAATTTTTTTGGCTCCTACTGAGGACTTGGGATTAGGCAAATGATAAATAGCTGGTTCTGGAGATCTTCTAATATCATTCTTGACCATATGCCAAACTGTTTCGATTATTTCTTGCTCGACGTAGTTACTTCTTATTAACACCCTTAAAGCAGCGGTGTGATACTCGATTGTTCGTTCCATAACCCGAATCCTTATTTTATCTAAAGAAGCTAAGCACTGGCTAATATTACCTAAAGAATCAGTTATATCACCTATCGTATTCTTATAAAATTGATCCGCCATTTGCCCAACGTCTCTCACTGCACCTTTAGCTTCGTTTGACCACTTCCCTAGTGATCCGCCAATTTTCATTCATTAACCCTCCTTAATAAATTTCACTGTGGTTAATGTTTAACTGATGAAATTAAAATATTCATTCTAATGCCTTTGAGCTAAAAATCTTACTTTATCTGTTTAACCATTGAACTATTAATTCCTTAGCAATTCGCTTCATCATCAATGGTGGTACACTCATGCCACATACATATTGCACATTAGCATCCATAAAATTATAGTCGGCCGGAAAAGTCTGCATACGAATAGCATCCATATCGCTGATGTGTCGCGGTTGATCCGTCCGTAAAAACACAGATGAACTGGCTAGAGTGTTCGCTACCTTCTGATCTTTTAGTAGGATCGTATTGAAGTTGCTTATTTTCCCTTCTTCTCGTTCAGTCACATCGCCCATATTCAAATCTGGTGGACGTCGTTTGTGCCAGCGGGTATATGTCTTGCTGTCTGGATTTATCAGAGATCCATCTCCACTACGAATATCTCCATATAGTATAGGCGGCTCGTTGAATTCCAATTGGAGCGATGGAAGGTTTTGATCCTCCCGAGAAGCGATAAAGAAAAGACGTTCCCTTTTTTGAGGAACGCCCATAGTAGCCGAGTTTAGTAGAAAGAGTTGTGGATTATACCCAAGCTCTCGAAATCGAGACAAAACCAGACTAACGAACCCACGAGCCTTACCAACCATCATTCCCCGAACGTTCTCAGCGACAATTACTCGAGGTCGAAGTTTCTCTGCAACGTCCAAGAAATCGAAGAAAAGATCATCCAGTCGCTGCACTGCCTGTCACTCGCGGAATGCATGCTCCCCACCCCACTTGTCCTCTCGATCTCCTGCCATGGAAAACACGCTACAAGGCGGCGAACCATCCAAGATATCTAGGTCAAACAACTCAGGTGGAAGCTCTTGATTAGGCAACGCCTTGAAATCCTGAATGGGCAACAAAAATGGATACTTCGGCTTATGATTCTGCCGATAGATCCGCATCATCTGTGGGTCGATCTCTACATTGCCCAGCACCGTGTATCCTGCCAGCTTATATCCCATCGTAGAGCCACCGCCACAGGAGAAGCATGAAAATACCGTTCTCCCATTCTTCGGGACGTTGGAAATTTCTGATAGCCGCCAATCCCATGCTGGACGACTCATGAGGCACCTTCCTGATCAAAGACAAATCCGCAGCGTGGGCATTTACAATCAAAACGAGATTCATCGAATTCACTCAAATCCAGCTCTCGGTTCTGAAAGTCTCCAAGCTGATCGGCAGCCGGCTCAGTGAAATCAGCGATTAACCTCTCGGCTTCTCCTGCATCAAAACCGGACAGCGCCAGATCAGCCCCACCCTCTTGCAGCTCACCTAGTAATTGCGCCAGCGCCTCGTCATCCCAGCGACCAGACACTTTATTTAGTGCCAGATTCAGCATCCGCTCCCGCTCCGGGTCTAGTTTGACTACTGATACAGCCAGCTCTGTGAGACCCTGCTCATTGACCAGCACCTTATATCGCTGATGGCCACCGACCATGTTGCCAGTCTGCTCATTCCAGACGATCGGGTCAATGTAGCCGAATTCATCCAGGCTGCGGCGAAGCTTCTCGTATTCTGGATCTCCCGGCTGAAGGTCGACGCGTGGGTTATAGATAGCTGAATTGAGTTGGTCAATCGGTATAATTCTGATGTCCATAAGGACCCTCCTTTGAGTTGAGTTGGATTTGGGATATGGGTATGCAAAGAGAGAGCCGTACAGCAACGCTGTGGCCCTGTCCTGACGCTTTATGCTCTTGTCGCTACATTCGAACACCTAGAACATACTTGCCTGTAATTGACTTATATAATGTTATATGAGCAAAAGAAAAAGCACCACAATGGGTGCTTTTATTAGAATTACAATTCTATCTTAATAGTAATATCATCATTTTTAATTACAAGAGTGAGTACATCAAACTGTATTTTTTGGTAGCTCGTAGACGCAGATCTTGAATATGTTGACTCAAGAACTTTAATTTGTTTTTCTGATAAATCGTGATCTTCATCTTCCCAATTTATTCCTACATTGTAGTACGGAGTATTGGCATAATGTTGCCCACTCAAAGATATAGTTACATCCTCTATACTGATATCATCGTTATCAGCAGTTTTAAATCGAACATTTGCCTTAAAAGTATACCCTCTTTTTTTATACAGATTATGAATTGAGTTATATTGCTCAAGAGCTTTTTTATCACTTAATTTCTCCCCCACTATATCCCCCCCCCCTTCGACATCATATTTCGACATCTAGGAAGTTTTTCCCTTCTGACACTTCACTCTTGAACAAAACTGTGCGGTTCCTTCCCATCTGCCCCATATGCACCCTGTACACTTATTCGGCTGCCGGGGCGGATCTTTTAACCACCGCTTCTTCTTCAAATCGATTCCCCCAATACAAAAAAGCCGCCCAATAATGAGCGACTTCGAAATATATATTCAATTCAATCATGCCATGAGTCCGATCTATAGAACGGCGTCCGCTCCGCATCCGCAGCAAATGCACTACGCTCTTTGCTTAAAATCTTTACGGACTTTGTAACAAAGGAGGACAAGACCATTCTACTGAGCCAATGAAATAAGAGTCAAAGCCACCAACGATGAATATAAGGCTTTAGTACATCTATTTACATCTCATTCTTTTTATTGCTCACTATTTCGCTTAAGCACTCGTCTTAGCATTATTGACTTTTTTAGCAGCCGTCATCTTCTCTCTCATTTGCAGAAGCATTTCAATAAGCTCTTCACGGCCGATGAGACGTACATTATTTGACTTTGCTAGCTTATAAGCCTGTTCAGTATAATCTCTGTTCGTTACAACCCAAGCAGCTGAAGCACCGTAATGTGAAACTGCCCCACGAACCTCTTGCACTGCCTTTAGCCCGACATTTTTACTGTAGCGTTTGGCTTGGACAACAATTTTTTTGCCGTCTTTGGATAAGACCAGATCAGCACCGTAGTCACCCGCTGCTTGTGTAACTTCAGCTTTGTATCCTTGAGATCGAAAGAGATGACCAAGGTATTTCTCGAACTGAACACCTTCCATTTTATCAATTTCAGCGATACCGGATTTCTTTAAGCGTTCAGCACGTTTTTGCCCTATCACAATCATTAATGCAACTACAACAGCCACGCCAACAACCGCTCCAATTATAGCCCCCTGTAAGGTTTTGGTTAAATAGTATCCTCCAAGTGCTAACCCCATTGCTGCTAAGCCAGCCACCCCTTGAAAAAACTCTTCTTCTTGTTTTGCCTTACTCTTTCTTCTTGCCATTCGAAACCCCTCCGCTATATCTTCATATAGTCCAATATTCGTCATAAAGGAAGGATTTTCCTCTTTTGGTGTCGAACTTTAGACCTATAAAAGAAGAAAATGGAGGTACTAATGGATTTCATCGAAAGATTAAGTGAAGCTTTAAAGCCAGTCGCTGTTGGGTTAATTGCTGGTGCTGCTGCAATCGGTATGATTTTCAAAGTGTTTGAATCATTTTTATAGAAAAAGCGAGAGGAGGTACGCCCCGGTTAATGCTGCAGCGACGCAGCCGTGCGTGTCACTCTCGCCTGATTTCCATGCTCTTATACTATCATGGGGAAACAGTCAAATGGTGTTCAACCTACAGTCAACTTGCAGTCATATTTCTCAAATAACATATTCAAAAGAGAATAGAAAAAAGGGATTATTTTAAAATCTAATGATTTGAAGGTGAAAATGTGTCAATTCAAAAGAATGTTGACGATTTAAAGGAATGGTATCATCAAAAACAACCTATTTACTCTAACCTTGCAAGCAAAATAGAATCTATTATTAAAGAACTCTTTAAAGCTGAAGGGGTTACATACTACTCAATATCTAGTAGAGTTAAGGATTTAGATAGTTTTATAAAAAAAGCACAGAAAGAGAAATATCATGACCCAATCAATCAAATTCAGGATCTCGCTGGGATTCGAGTAATTACTTATGTTAGGAAAGAAGTAATCAAATCTTGTGATATAATAAAACCTTTATTTAAGATTGACGAAACTAACAGTGTAGATAAAAGTAGTGAGTTGGGGAAGGACAAAGTAGGATATCGCTCAGTTCATTATATTGCTACTTTAACGGATGAAAGATTAGCCTTGCCGGAATATAAAATGTTCAAAAATTTAGTTTTTGAGATTCAGGTTAGAACATTACTTGAACATGCATGGGCGGATATATCTCATGATAGAAGCTATAAATTTAAAGGGGATTTCCCTCCAGAGTATGATATTGAACGTCGATTTGCTCTGGCATCAGCAACATTAGAACTTGTTGATAGAGAGTTCGATTCTATTGTAACTACTTTAGATAAATACGAGAATGAAACTGAGGAAAAAACGAAAAGGGGAGAATTAGATTTACCTATTAACGCTACTTCCGTAAACAATTACTTATTACACACCCTTGCTAAATATATTGAAATGGGTAAAGTTGAACCATCTTTTAATGGTGCTGAAGCAAATGTTATTGATGAATTATTGGATTTTGACTTAAGCAATCTAGGTGAACTCGATCTACTCATTTCTAGATTTCTCAAAGAGGCACCAATGATTTTTGAGCGTACAAATTTTGTTGGATTGTTAAGGAATTTAATGATGCTTACTGATACAGATAAATATTTTAATAAAGCTTGGAATCAACATTGGGCTTCGATCGATGCTGGTTTTTTACAAATAGCTAGTGATTATGGTATAGATATGGGAGATTATATAGAAAATAATCAAATAGACATCTATGTAGATGAAGAATATGGTTATTACATTGATCACGAGGATATTTGAGCATGAGAGAACCCAGTTTTAACATAATAATTTTGTGTTAAAACTGGGTTTTGTTTTTAGAAATAATAATAGGTGAGCACTGTCAATCAAAAAACTTAACCCCCACATATTATTGTCAATCAAACTTCCTCGTCATCCTTCTCAAAGAATCCCATCAGCTTCAATGTATTGGAAATACTCCTGATACCCTCATCGAGTTTACGCCGAATAGTACTGTCACTGAGACCGTAGCGGAAGAATAGTATTGTCTCCTTAAAAGAATGTCCCTCAATATATCTATGTTGAATCGCATCACGTGCCTCCTTGTCCTGGATCAGACTAGTTGCCCGCCGAATAACCCCGGTATAGAGCTGGTACTGCTCGTACACCCAACGTTGTTTTTCGATTAGAATAACGGCATTTACAGTCTTGTCAGCGTGCAGTTCATCTTGATCAATCCGTCGTGCGACTTCTCCGTCAGTAGCCACTTGCTGCATATCTCGCGTGAATTTTTCGTAATCATTCATTAAAAGTAGCATACTTTTACATTTACAAAGGAGGAACTTTGTCCGCTGGATCTCTGTCTCACTCGCTGTTGGAAAAAGCTCATCCTGTTGCCAAACCATCGCCATCCCCCTACTCCCCTTTATGTTATAATATCAAGAGGAATAGTTTGGTAGAATGACCCCCGCCCCAGCCAAGGATATGGGGGTCTTTGTATGTCTCAGTATTTTTCAAGCTGCTTAAGCTTCTTCCGCAACTGCACATTCTCCAGCAGTAACCTCCAATTTTGCTCTCTTAAATCTTCCTGTGACTGTAGCGAATCGCTAGTTTTCTGCCCAACCACACGTAACGTCCGGACTTCATTATCCTTCTTCACTAAGTACCCTTTATCTACTAATTGTTTTACTAATGAATGCGCAGTAATAGGCAAGCCGCTGCATCCGCACTCCCGTCCATCACAACAGTATTCAGGCTCATATTCGATGGGTTTTCCGCATTCCATACACTTATCTGCGCTGTATATCTGTCTTCTCCCCCTTCCCTTTTTCTCAGGGTCACCCGGACCTCGCCAAAAGCTCTCTACTTCATCCTAGGTTGCGTTTTGATATTTTTCTTTTCCGTTTTAACCACTCTTTTTTTCATATCCAAACATATTATTTTATATAACTAAAAGAAGGAGGAACAAAAATGCTTAGTGTTATCAACTTTAATAATTCTCTGCTTACGAATTTGGACGACACTGGAATCTCTCTTACTACCGTACCGGGGTTATTACTCGAATTTGGTATATTCGTAGCAACACCAATAAACGTTCTAAACATTCTTTCGTGTATTGGTTCCGATCCACCCACTAATTCAGTTGTTGCAACTTTTGAAGTCTACCTTGATGGTGTGCTTACGGGACAAACGATGATTGAGGCCGTGAACGAATCCCAACAGATTACTTTTTCAACGATAGTGTCGAATGTAACTCCAGGCCACCATGTTATCCAAGTATTCGGTTACGCGGATACAGCTAATGAATTTATTTTAGGTGGTCCTATTAACGCTACTGCAACAGTGTATGGGTAATGGTTTGATCGGCCTCATTCATCTTAATGAGGCTGACTTTCATGTCCTTCCCAATTCCAGTCTTACTGCAGGTGCATTTCAATAAGTTCAGCACCTTTAACCATCCAAAATGCTCTCCTTCCGGTTAACGTTTGCTTCGCTTTCTTTCACCGATTTTCTTAATAATGTCAGCCAAAATAATACCGCTCCGCGTGAGCTCCGCATCCTTTTGGATAAGTCCTCTTTTATTCATGATGGCCAGCTGCCCGCCGGAAACCATGATCAAGTTATCCGGATCGAAGTTCCGCCTATCTCCATCCCCGAAAATGACTGCATGCCCCTTCGGAACCGAGCGGCCGCAGTGCTGCTCCCAAACGATTAGATGCTTCCTGCGCCACATATTCGGATCAGCAATCTTTATATCTACATAATCATCCCCGTTAACCCTCTCAGAGCCTACAGAAACATAATTGTGCGGCTTATGGCCCTTCTTGAATTGAGTATCCTCACCGCCGGTCCATAACTTCTTCTTTCCCTTATTGGGTGGAATGCTACCCGGTTTGATCCTGGCATCGATTCCGCTCTTCAACCCGTTATTTTTGATGAAGGCTCTCATTTGAGAAGGCTGGATCTCCACGTCGAACTTCTCATTAAACATTGAAGTCAATTCCAGAACATATCGTCCATGAATGTTGGTGCTGATAAATTCCTTGTGCTCCAAACTGTATCGGAACATTGATTATCCCTCCAGCATCTTAGGGATAGCCGTATTTGCATTCATCTTGTCATCAGAAAGCTTTATTGCATCTAGCACAAGGGAACCATTAGCAATAACTTGAGAAGCGACACTCGTTACAGCCTTTGCTCTGCTAATCTCGTCAGCCAGTTTCTCTCCGGTCAATTCCTCATCACTCAGGCGCTCTAATTGAGCAAATAAATGATTATTCAAATCTCCCAATGTGTTTCGCATAGTCGACCTCCCACTGATTTGAATTTTGCATCTTCCGCCTTAACAATTGTCGTTAGACATAACATTGTTTCCATATTATTGAATCTATTCTCCTAAATCTTCGTAATAGATTCGAGGTGATACAATGATATTTAAAAAAATGAAACGTTGGGTAAAGATTGTATTTGGACTCCTATTCTTCTTCACAATACTAGGAGTAACTGGGTTGATTGGCATCATGATTTTTCTAGCTTTCATTGATGACCAGGCAATCACCAACACAGCTTTAATTAATAGACTCACTTTGCTTCTAGCAGGATTATCTTTACCTGGGTTGATTGTCCAACTCCTTTCATTCCTCACTATTAATGATAAAAAAACTTTTACCTTAGAAAAAAAGTGTCCCCATTGTAAGCAACTCATTGAATTAAAACTTACCGAAGATTGAACGGATGGGATTTACTCCATCCGTTCTTTAATTACTCCCATAGGGGCAGTTTCTTTACCCTTACCCGTAGCCCTTCCATCGAAGGTTTCGGATCACTAACAATGAAATAATCTCCATTATGCTCCACATGAGAGTACACCCAGCGACTCTCTCCTGTGGAATCTTCGGACAAGTATTCAATAGAAGAACCAGACGTATAATAAGCATGCTTTCCGGTTGTGTACCTACCATCTTTCCCTTTGTGAAGAATACCTTGTTCAATCAGAGGTGCCGTCACTTGGCGTATATACCGCCTAACCTCGTCCAATTTACTGCTAATCTGATAAAACATCCCCCGAAGATACATCTCTTGTGGATCCCCTTGGTTGTAACCTCCCTGATTTTCAGCTTCATTGATCATATTTGTAACCCACTTAATTCGAGGTTCCAGCTTCTCTAGCTCTACTTGTATTAGGTTTTTCATTTCTTCACTCCCCCTTCCTTAATACATTTAACTCCGTCGAATATTGATAAAAGGTTTCTCTATCTCGCTCATCTAGCGCTTGGTCGATCAGTGTCCGTAACTGCGCAATCCGATGTTTCCGCACTGCCGTTTCCCACACAACTTCGATATATTTATCAATTGCCAGTGCATAAACCCCAAAGATCAAGGTGGCACCTCCCTAGGTAAGAGAAAAGCAGCTTACGCTGCTCCTCCACCACCCTTCATTTTCTTTGCTGCCAGCTTGCGATATGCCGTCCATCTGGTCGATAGTTGCCCACTGGTCATGCCATTTTCACTAGCAATTTCGCGCCATGTCTTATCTTCCTTGATGCGTTTCTCCAGAAGAACAGGGAATGGGATTGGCTGTCCATCATATTCGACTTCAGGAAAAATTGGGCGTTCCGCAAGGATAAAAGCATCCAGTACTTCCTTACTCGTCTCATCTGCAACAGCTTCACGTAGATCAGAGCTTTCACCTTTAAAGACTTGTTCCCCTGATTCATTAGGATCACCCTCGTTATCTTGGCTGTCAGTTCCAGCTCCATCATTCAGCCAATCCGGTTTGAGGTCTGCGCCCTCTGAATGCTCATCAGAACCGCCATCATTTATATCTTCTTCAGATGATTGAACGTCATTAGCTCCTTCTTCTTCTGCATCTGGTTCAACAATTTCAAAATTATCATCCTTCTGCTCGCCATCCGAAGCACCTTCTTGCTGTTCGAATAGCTTGCCTTGATCTGGATCTTCTTCACCAAGCTTCTCTGTGCTCATCACGATACCGGAAGCATCAGTTGTGACACGACGGTCAGTGACTTCCCGGTATATATCTCCGTCCTCTTCATCGAAATCAAAAGCAGCCTGCGGATCTCCCATGAAGACATTGATCTTTTCCCCTTGATTGCTGCTGAGGAACAAGAAATTTTCTTGCATAACCTTCAGTGGCACAAGCAATTTAACTTCAACGTCGGCATCTCCAACTTTAATTCCTTTAGCAATAGTTGCACTGAATTTTGCATAATCCTTTATCATATCGATCTTCCCCTCAAGTTTTTTATTGGAGTTGCTTGATCTTCACTTCAATGCGTGGTCGTGCGCTGTACCGTTTCCTTACGTATGCGTCCACAACTTGGCTATCATCCTTCCATATGATGCCTTTCAGTGCATCCTTAACACCCTTCAGATAGTTGTCTGCATCAGGCTTAGTCACTGGAAGAATATCACCACGCGATGTACAGCATAAAACATTCTTCCACGAGCTTGGACACGTGCTCCGCCATGTTGGGGATCAGCGTCAGATTTCGGAGCTTTTCCAGCAAATGCAAGAAGCTGATGCCGAACGATTCAGTCTTTACGCAGCCATCCCCTTTTTCATGCTTGAAAAATTGCAGCTCCCTGCTTTCGAAGAAGAAGCGGCAGGTATAGTTGCAACCGTATTTCAGGTTCCTCCAGAATTCGCACTGTTGCGTCTGAAACAGATTCGCGAGCGTATTGCTAGCGCTGAATTCATGACGGCTTTTACATATACTGCTGTGGCCAAGGAAAACACTTTACCATACACGACAACTCCTGAGCCAATCATACGAGGTGTTTACGGGCTTGACGATTTATCTAGACCCCACACGCTTATCATTGAACAACGTGGAGGCTTTAAGTGGGATCAGCCACTCTACATCGAGGTTAATGGAACCTTTAAAAGCGTGGATGTCCATCCAAACTCTAATCGGAATAGCGCTGTTGTTCGTTCAAGTGATCTTTTAATCCCTCCGAGCCGTTCTGGATACGTAATGATCGACATGGAGCGAATTGCTTCTCGACATGGACAAAACGCAAACAAATTGTTTCTAACCATAGAAGCTTTAGAAGATGCTATTAATTTTTAATTTAGGAGGACCTACTCATGGCCAGCGTATTTAAAATACCTGCAAAGAACAAACAAGGCTACAAGTGGAAGTGTGTCATGGAGGGTCCTCCTGATCCGGTCACAGGCAAGCGCCAACAGGTACCGAGGGTACGTGATACACAGAAGGAAGCCATCGCCGCAGCTCAGGCAGTTGTGGATCGTATGAAGGGTGGAACAGATACAAAGCGAGCCAAAAAAATGAAATTCAATGAGGCTGCTCAAGAATGGCTACAAGATTATATTATTACTAGCGGAGTTAAAGGAAAAACTGTGGAAGCTCATGTGTCCGACATTAATTTGCTGAACAAATATTATGGTGGAGCTAATATTGATAAAATAACACATAACCAACATCAAAAAATGCTCAACAATTTGTTTTCAGAAGGATATGAAATAAATTCCATCTATCGTTATCACTCAACAGCAAATTTAATTTTCAAATGGATTATCAAAGAAAATTTACGCATTGATAATCCTTGTCAAAACATTAAAATGCCTAAAAAACAAAGGACAGTTTTAGAAGCTAAAAACAATGCACTGGAAGAAAAATTTCTGGAAAGAAGTGAAATTGAAGAATTTCTGGAAGTACTACAAAATCACGGTTTAGGTGATGATCTAGAGACGTTTTATTTTTTGCTGTTTAGCGGAGTGCGACCAGGAGAATTTTGTGCTTTAGAGTGGCCTGATTTCAACTTCGAAACTCATGACGTTCATATTTATAAAACACTTCACTTTCCACAGGGTGGAAGTGGCGCGTACCAATTAACACCTCCAAAGACTACCGGATCCGTCCGCACCTTTGATGTGGATGATTTCATCGTTGAGATGTTTAAGCGGTTAAAGATAAAACAGTCCGCTCGACATAAAAGATACAAGGAGCTCCACGATGATTTTGTAGAGACTCAGTTTATTTTGACCAATAACAACGGAACACCATTTACAAACTGGAAGTTAGTTAATCGTATGGCTCGTCTAATGAAATTAACAAATATCAAGAAGCACGCAACTCCTCATATATTTCGACACACGCACATCACGATGCTAATCGAAGCAAGTATCGCGTCTGGCTCTCAGATTGATCTCAAAACGATTATGAAGCGTGTAGGTCACGATGATGCAAAAACCACACTCAATAATCCCAAGGATCTGCCGAGAATGTGA

Protein sequences of DBSCAN-SWA_5

>NZ_CP009279|3665223:3692488|3667652_3668129_-|WP_042188665.1|DBSCAN-SWA
MMDVGLKAWAELVQRIYPELPILRDRSLWLAGQFDRPSVFIETDLVSDKAHTPRADRIIEDVGLVFHYDIDRSVVEEDGEPIPLDLSPFFLYLRQRRFCVVSKRFGIMMVIEAPRTRPQNDRMEVTFRYSFLTHVPKLMIRDDGRQIQKINDFFIEPS
>NZ_CP009279|3665223:3692488|3686132_3686624_-|WP_042188695.1|DBSCAN-SWA
MAMVWQQDELFPTASETEIQRTKFLLCKCKSMLLLMNDYEKFTRDMQQVATDGEVARRIDQDELHADKTVNAVILIEKQRWVYEQYQLYTGVIRRATSLIQDKEARDAIQHRYIEGHSFKETILFFRYGLSDSTIRRKLDEGIRSISNTLKLMGFFEKDDEEV
>NZ_CP009279|3665223:3692488|3668606_3668933_-|WP_042188669.1|DBSCAN-SWA
MNHRMNTPLAVYRVGRQQDAENLFSDRKVGKIADLKGFVVKTQTDAKADSTPVIYIVKKTIGVPKTADVQISDEVLLFGRKYLVIDSNPRRYWRELLVTCEVKGSERA
>NZ_CP009279|3665223:3692488|3668929_3669316_-|WP_042188672.1|DBSCAN-SWA
MLEATLLKKRSRVSAVQEATDVQLQQYIDDAQTRIELYLPVPFPEVADKQLMLAWVKLAESLALQDSEEYLASVARGYSAESEGAWTYTRQAVEGKTTGNADVDSILFLWVKKQQSGPDDGNITAYLL
>NZ_CP009279|3665223:3692488|3690478_3690643_-|WP_081951287.1|DBSCAN-SWA
MLPVTKPDADNYLKGVKDALKGIIWKDDSQVVDAYVRKRYSARPRIEVKIKQLQ
>NZ_CP009279|3665223:3692488|3689410_3689593_-|WP_042188709.1|DBSCAN-SWA
MIFGVYALAIDKYIEVVWETAVRKHRIAQLRTLIDQALDERDRETFYQYSTELNVLRKGE
>NZ_CP009279|3665223:3692488|3679674_3679884_-|WP_042188687.1|DBSCAN-SWA
MGTQDEILLQHELEVMAGILESKAQYRKIIKAGIAKWVKDFQDGRIEIKTVDDLKKLIEIDIELQKDEL
>NZ_CP009279|3665223:3692488|3679033_3679678_+|WP_042188685.1|DBSCAN-SWA
MSEYYPPMHLKESFHCIFCNVYTTHEWIRTYRQVPMGYSQLSELYVCMCKHCNKKSYWHDEKMILPSSAGAPNPHEDMPVVLIDDYLEAKGIVNLSPRGSTALLRLVLQKLMIELGESGKDINKDIGSLVNKGLPEEIQQALDIVRVIGNESVHPGELDLRDDLETALQLFELINFIIEERISRKKRISSLFSRLPEAKLKGIEVRDKDKPVTT
>NZ_CP009279|3665223:3692488|3688655_3688943_+|WP_156113125.1|DBSCAN-SWA
MKRWVKIVFGLLFFFTILGVTGLIGIMIFLAFIDDQAITNTALINRLTLLLAGLSLPGLIVQLLSFLTINDKKTFTLEKKCPHCKQLIELKLTED
>NZ_CP009279|3665223:3692488|3669598_3670546_-|WP_042188674.1|DBSCAN-SWA
MRTNGNIANTSIRKSTIVTPMDQNALNYEEVEAFTDMAYEANGFLKGIRHENRKSSKGTIDKVGVRGRNMRSKKENIMASNTPGLTFPQIPYSVEPVIVPFDITEEFIRQTQRVRGQNAEDIIMRAMANNYGENMQDIGFNGDTATSNTDPDYEFLCINDGWLKKARTTGHYLDWKTLSAKEKTGILFEVERAIPTRYRAGGVFKYFMHPNTFSERLQMLAEKDTSASIQLQILGGTKKVNAYEVEEVWSMPEGSILFPYQPNFAMVHTYDMQIRKTTEGKEAIWTDKRFYAIHSDFDAIFEEPQALAYVEGVEF
>NZ_CP009279|3665223:3692488|3675236_3676715_-|WP_042188682.1|portal|DBSCAN-SWA
MSGEAQWFQISKAEERHIPSSAQLSDSFENLYDQHGLLPFPPGNDPASCKLLVKNSNIIPQCIEAYKRNIAGYGIALEYLPGESDQTAQEEWNKADKFLETCNLEDTPDEIIGSLIEDIESSGNANVEVAWPAGSEFPTLYRINPKFVRCKRETDKVTIKRKRLIRSSKKIEEFSQDIYARKYAMKRGQSVVWFRPFGTEGQGNQIIPLKLGNDGPYGEPRWFGNAPGVVGSREAEELNVSYFSNGRMLSMLLTVTNGRLTKQSMELLKNVKGSQSQGGILYLEAIGEETGGPLDEKVEKVSIKLDKLNDLLQQDALFLEYGKDKKADILSSFRLPPILVGQSSDYNRATAQAALRFAEEQVFEPYRKWIMDEIFNKRLFPAMGIFRVRATLRGPRIIDPEDRKALLDFIADRGIMLIRDLIPIAEEVLDTTVDESKYTDEYLDTPIAQLINSQHALTVPEPDSDVNDLQEQVSTIAKRLLRQSHDEVTGHV
>NZ_CP009279|3665223:3692488|3686716_3686998_-|WP_042188697.1|DBSCAN-SWA
MECGKPIEYEPEYCCDGRECGCSGLPITAHSLVKQLVDKGYLVKKDNEVRTLRVVGQKTSDSLQSQEDLREQNWRLLLENVQLRKKLKQLEKY
>NZ_CP009279|3665223:3692488|3666556_3666802_-|WP_042188660.1|DBSCAN-SWA
MNLKKQIRQPTNVVPDTLNKRSKQEWIESAVVLKRERFEIAGALFDCDDDTLLSQQEVIQKVKAYLGLTKKEETVNVDTTE
>NZ_CP009279|3665223:3692488|3687183_3687567_+|WP_042188699.1|DBSCAN-SWA
MLSVINFNNSLLTNLDDTGISLTTVPGLLLEFGIFVATPINVLNILSCIGSDPPTNSVVATFEVYLDGVLTGQTMIEAVNESQQITFSTIVSNVTPGHHVIQVFGYADTANEFILGGPINATATVYG
>NZ_CP009279|3665223:3692488|3684924_3686013_+|WP_052404310.1|DBSCAN-SWA
MSIQKNVDDLKEWYHQKQPIYSNLASKIESIIKELFKAEGVTYYSISSRVKDLDSFIKKAQKEKYHDPINQIQDLAGIRVITYVRKEVIKSCDIIKPLFKIDETNSVDKSSELGKDKVGYRSVHYIATLTDERLALPEYKMFKNLVFEIQVRTLLEHAWADISHDRSYKFKGDFPPEYDIERRFALASATLELVDREFDSIVTTLDKYENETEEKTKRGELDLPINATSVNNYLLHTLAKYIEMGKVEPSFNGAEANVIDELLDFDLSNLGELDLLISRFLKEAPMIFERTNFVGLLRNLMMLTDTDKYFNKAWNQHWASIDAGFLQIASDYGIDMGDYIENNQIDIYVDEEYGYYIDHEDI
>NZ_CP009279|3665223:3692488|3683070_3683427_-|WP_156113123.1|DBSCAN-SWA
MGEKLSDKKALEQYNSIHNLYKKRGYTFKANVRFKTADNDDISIEDVTISLSGQHYANTPYYNVGINWEDEDHDLSEKQIKVLESTYSRSASTSYQKIQFDVLTLVIKNDDITIKIEL
>NZ_CP009279|3665223:3692488|3689625_3690456_-|WP_052404311.1|DBSCAN-SWA
MIKDYAKFSATIAKGIKVGDADVEVKLLVPLKVMQENFLFLSSNQGEKINVFMGDPQAAFDFDEEDGDIYREVTDRRVTTDASGIVMSTEKLGEEDPDQGKLFEQQEGASDGEQKDDNFEIVEPDAEEEGANDVQSSEEDINDGGSDEHSEGADLKPDWLNDGAGTDSQDNEGDPNESGEQVFKGESSDLREAVADETSKEVLDAFILAERPIFPEVEYDGQPIPFPVLLEKRIKEDKTWREIASENGMTSGQLSTRWTAYRKLAAKKMKGGGGAA
>NZ_CP009279|3665223:3692488|3688974_3689406_-|WP_042188707.1|DBSCAN-SWA
MKNLIQVELEKLEPRIKWVTNMINEAENQGGYNQGDPQEMYLRGMFYQISSKLDEVRRYIRQVTAPLIEQGILHKGKDGRYTTGKHAYYTSGSSIEYLSEDSTGESRWVYSHVEHNGDYFIVSDPKPSMEGLRVRVKKLPLWE
>NZ_CP009279|3665223:3692488|3690611_3691307_+|WP_081951136.1|DBSCAN-SWA
MSASGLVTGRISPRDVQHKTFFHELGHVLRHVGDQRQISELFQQMQEADAERFSLYAAIPFFMLEKLQLPAFEEEAAGIVATVFQVPPEFALLRLKQIRERIASAEFMTAFTYTAVAKENTLPYTTTPEPIIRGVYGLDDLSRPHTLIIEQRGGFKWDQPLYIEVNGTFKSVDVHPNSNRNSAVVRSSDLLIPPSRSGYVMIDMERIASRHGQNANKLFLTIEALEDAINF
>NZ_CP009279|3665223:3692488|3678021_3678927_-|WP_081951135.1|terminase|DBSCAN-SWA
MARERSPERDKAKQMWLENGGTMKLKDIAAALFVGENKVRKWKSIDHWEEELKGNVPPESKGSVPVEMKGNVPNRGAPKGNRNAVGNRGGAPTGNKNAKGNSGGAGGPVGNKKAVTTGEHETIWLDTLTETEQQLIDQVDTDPINQANESLYLLAIRERRMMHRIKSLMDGLSETERSVLYEMKAIKEVAEIYDEKTGITKKIPHSRNEMMESKIEEKGFRKIDDIVKLEEALTRIQDKKIRAIELKNRLIDDEKRIRIETMEYELQMLRGGGGKEAFEDDGFIDALKGMAAGVWSDDGEA
>NZ_CP009279|3665223:3692488|3680080_3681208_-|WP_042188689.1|DBSCAN-SWA
MKIGGSLGKWSNEAKGAVRDVGQMADQFYKNTIGDITDSLGNISQCLASLDKIRIRVMERTIEYHTAALRVLIRSNYVEQEIIETVWHMVKNDIRRSPEPAIYHLPNPKSSVGAKKIDIASHVFPKNKYPSILVHGMGYNASLDDAYSFYRDFEDHVDVFSDSRYADHDIYLVSYDTELTDESDSIIRAAIELLLGMIPGGDLEPLVLGVFWRELERRASLTGDYIFPFLKRIKQEVPTALGFAVTHSLGCFTLASASQKLLSENRNNKIFSKWLCMAAALPANAFTETGSFSLAPLIAGYPDGPKYGTSVWFSRLDLVLNIAYTLANRHLAMGVSGPLQKTVTSSVDVTNTTKEDHYQAYFKKLSQMLKELFGI
>NZ_CP009279|3665223:3692488|3668125_3668620_-|WP_042188667.1|DBSCAN-SWA
MSVHDFDGLAKKFKKLSDEGVSQILKNIAEAVGETLLNLVIDEIDKQDLIDTGLMWNSFTRGEENNIWEWDIDRNSITIEVGSNVPYARHLNDGYTIHKAHFVPGYWATNGTFVYDPRAKGGFMAKPRSFIGRHYFDIAVQQLEGGMNALIMKRLEKELGRMLS
>NZ_CP009279|3665223:3692488|3673432_3673963_-|WP_052404309.1|DBSCAN-SWA
MDVINKQDIKKARKGDHEAFIRLITEIKLPMYRMARTLLNTDEDCGDAIQETVLKAYKALHSLQQPDYFQTWIFRILINECNRILGNQHKQGEADEIKRITYIEPGYENIDLRELVNDLDEPLRIVVILHYFHDMTMKQISNILDLTEGAVKTRMYRARKQLLEWLSNSERKEHEA
>NZ_CP009279|3665223:3692488|3670567_3671794_-|WP_042188676.1|terminase|DBSCAN-SWA
MSYKLKDAKITHISLVDKGANGVPFAIIKSAGKNAIQKQVQIAKIDDDKRIVKGVVYQPDVADAHDDQMDEVEIEKAAHLFMEKQHTYNIDKQHDLEADKGFVIESYIAPCDMTLGEQEIVKGSWVAAVKVTENDTWEAIKKGEITGFLMWGVGKREEIEEEEEVSKGILSRIAKALGLIEKGAVADKYHKNRKNREFWAAQDALNSVLFNWDSYNSGMETDVDTIREALQDFVDIAQDVLTKEDIVKAIGTPPEQIAKAGKKISANNLKHVDDAIAALTELKNKTAPVEQEPEEDDDLKAEDIAKAVTAALAPIAKQVEGLTSEIAELKKEEGVEGDQPACGVTPAATVEETAITDAIAKALAPLSEQMQTLAADVQLVKNSRGASAQGEQEEISKSEGAVSFGRFL
>NZ_CP009279|3665223:3692488|3666871_3667546_-|WP_042188662.1|DBSCAN-SWA
MPEYSQIQTYLKCDQKNFKEIILHFSNVLKSLSLESKYFSPELEYEVSDNGFMYVGGDAESQIFDYNEHPFHIRPYVMGWTPKAISELEESWLEVSLLFWTEEIELDYRTGQLKDEIKSLVWSMLSKFSEEFKQTGVYFTNEVTDGIPWEAVVCSKKDEVWAFDAAILPAHLFDVYKDGYEEMFIYTNDNNTLYAARKSVWSIEPWLDDCTINEEQEPATGNVD
>NZ_CP009279|3665223:3692488|3674413_3675244_-|WP_042188680.1|DBSCAN-SWA
MCKECWELIAKADDTEFLDSLELTNAERAVLEELYKQGENRIVEILELQGKALHDAILELSEELLLDIGELGKVIQSVQSGDLFTVQFEQAVYDSFTPLFHLAGESELTVLNNDKTWSTKNKAASRFAKNLKKLVPDMNGTSKDVMTRAFQKAIKEGKTPSERALLVREISAAAAKGDAGPFNMERAITVSRTMSTAAANGGKLEGWKQSEVVTGKKWRSSKGDRTRKTHRKANGQVQPLDKPYEVGKSKLMFPGDPSGRAEEIIKCRCTMQSVLK
>NZ_CP009279|3665223:3692488|3676718_3678035_-|WP_042188684.1|terminase|DBSCAN-SWA
MAKLKLKPAAFKWSPFSNKQLKVLTWWTPESPHHDKDAIICDGSVRAGKTVCMSFSFIAWGMDTFRGEQFGMSGKTIGALRRNVVGPLKRMLASRGYHVHDNRSENVLTVTRGLISNRFFLFGGRDESSQDLIAGITLAGMFFDEVALMPKSFVDQATARCSVDGAKLWFNCNPAGPYHWFKKEWLEQLQKKHALHLHFTMEDNLSLSERVRERYRRMYSGIFYQRYILGLWVMAEGVIFSKFNDAIHKKPRDWFPSKFDRKFICIDYGANNPTAFLKYGVNGNVYYELDEYYHNIRHKGEKTNGEYADYLEAFLDGDEYSIFIDPSAKAFIIELKKRGINNIRAAVNTVLDGIQTVSNRFQNNELYICADNTNSLQELVSYVWDEKAAERGEDKPIKQNDHTCDARRYGIHTDYLLQRVKQRKKEREERSDHDVGWV
>NZ_CP009279|3665223:3692488|3665223_3666576_-|WP_042188658.1|portal|DBSCAN-SWA
MSIQRNRPGAYVELQAVAKSRVLSVSGRVLVPYQAEWGLPNKAVDMADQSERLKESELLVDELELAAENGATVIGYRVTNDSEVAASVAVASSYTIEARYPGTRGNDFEYLIRASLVDATKKEIVVRDTKGIYDTETFLVADKTEAINALKKSNMVRFKDTGSTALADVAYTKLAGGVTGTAAITAANWSGILNRIDGLVFDVVYLPSSDAAVQAAAKQWLLDRRSKARKLAQLVIAGASGADDDIEAHNTRSRAANARFIINCSLAGEHSNGKTYTSLQWAAWVAGLAAGTPANKSFTGVKVPMTEALVDWSHSEVLKGLAEGTLMATRDGYDYIIESAVNTLTTLGAGEREDFGKIRVSMTIDQILNDIYFAGKTNKAKLDNDKDGRGMFIAAVVSYLKTRAEQKAIGSEFTFTEHPTKKSDMDYAYFSLSAKPLDAIEIFNIDWEVA
>NZ_CP009279|3665223:3692488|3688285_3688516_-|WP_042188703.1|DBSCAN-SWA
MRNTLGDLNNHLFAQLERLSDEELTGEKLADEISRAKAVTSVASQVIANGSLVLDAIKLSDDKMNANTAIPKMLEG
>NZ_CP009279|3665223:3692488|3682333_3682870_-|WP_042188690.1|DBSCAN-SWA
MDIRIIPIDQLNSAIYNPRVDLQPGDPEYEKLRRSLDEFGYIDPIVWNEQTGNMVGGHQRYKVLVNEQGLTELAVSVVKLDPERERMLNLALNKVSGRWDDEALAQLLGELQEGGADLALSGFDAGEAERLIADFTEPAADQLGDFQNRELDLSEFDESRFDCKCPRCGFVFDQEGAS
>NZ_CP009279|3665223:3692488|3691324_3692488_+|WP_052404313.1|integrase|DBSCAN-SWA
MASVFKIPAKNKQGYKWKCVMEGPPDPVTGKRQQVPRVRDTQKEAIAAAQAVVDRMKGGTDTKRAKKMKFNEAAQEWLQDYIITSGVKGKTVEAHVSDINLLNKYYGGANIDKITHNQHQKMLNNLFSEGYEINSIYRYHSTANLIFKWIIKENLRIDNPCQNIKMPKKQRTVLEAKNNALEEKFLERSEIEEFLEVLQNHGLGDDLETFYFLLFSGVRPGEFCALEWPDFNFETHDVHIYKTLHFPQGGSGAYQLTPPKTTGSVRTFDVDDFIVEMFKRLKIKQSARHKRYKELHDDFVETQFILTNNNGTPFTNWKLVNRMARLMKLTNIKKHATPHIFRHTHITMLIEASIASGSQIDLKTIMKRVGHDDAKTTLNNPKDLPRM
>NZ_CP009279|3665223:3692488|3683875_3684487_-|WP_081951286.1|DBSCAN-SWA
MARRKSKAKQEEEFFQGVAGLAAMGLALGGYYLTKTLQGAIIGAVVGVAVVVALMIVIGQKRAERLKKSGIAEIDKMEGVQFEKYLGHLFRSQGYKAEVTQAAGDYGADLVLSKDGKKIVVQAKRYSKNVGLKAVQEVRGAVSHYGASAAWVVTNRDYTEQAYKLAKSNNVRLIGREELIEMLLQMREKMTAAKKVNNAKTSA
>NZ_CP009279|3665223:3692488|3687691_3688282_-|WP_042188701.1|DBSCAN-SWA
MFRYSLEHKEFISTNIHGRYVLELTSMFNEKFDVEIQPSQMRAFIKNNGLKSGIDARIKPGSIPPNKGKKKLWTGGEDTQFKKGHKPHNYVSVGSERVNGDDYVDIKIADPNMWRRKHLIVWEQHCGRSVPKGHAVIFGDGDRRNFDPDNLIMVSGGQLAIMNKRGLIQKDAELTRSGIILADIIKKIGERKRSKR
>NZ_CP009279|3665223:3692488|3672353_3673436_-|WP_042188678.1|DBSCAN-SWA
MNDFQLKNKLLELRAEEPEIIPEIVELKLMEAFAELEPIKKTASNKRKVTLVAAAAAILFVCLFSSAFVSTTIAQTLKGIPIMDRLFKLTGNVGLETADQRGLLSKTSYSITHNEFTLSIKKVIYTGSNVSFVLHMKNNEGGSVPVKYEAFVKIDGKDFPMILSGGHTQIDESNPSEGAAVISVSHSEVDSGTGEMYSFPETFQLGFTLLLNGMEEMPFQFEIPVEKTAEVYKVTPPHAEKTWNRVKLTVKSLEFTPIMTQLVVNIENSDEIEKLTEGRYFDYVIEDQSGNIVEKSGGLAGTLIPGTEVFSMNAEFRPFDDVPQSVIVKPYISIYKQEDDTMKRMYIPELEMLIEIKPKD
>NZ_CP009279|3665223:3692488|3669293_3669599_-|WP_042193994.1|DBSCAN-SWA
MPYVTYRGKNASLRLYSIRFEPAKPVLVEDSVVLEKLHEHPDFEVNAEKVIPLEDLTVPQLKDKAKKAGIEGFADMKKPELINELKALEGGGVPNAGSDTP
>NZ_CP009279|3665223:3692488|3683548_3683704_-|WP_156113124.1|DBSCAN-SWA
MRSGRRSIDRTHGMIELNIYFEVAHYWAAFLYWGNRFEEEAVVKRSAPAAE

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
3660932:3660946	attL	NA	NA	NA	NA
WP_042188658.1|3665223_3666576_-|portal	phage portal protein	A0A2H4J187	uncultured_Caudovirales_phage	4.3e-20	29.3
WP_042188660.1|3666556_3666802_-	hypothetical protein	NA	NA	NA	NA
WP_042188662.1|3666871_3667546_-	hypothetical protein	NA	NA	NA	NA
WP_042188665.1|3667652_3668129_-	hypothetical protein	NA	NA	NA	NA
WP_042188667.1|3668125_3668620_-	HK97 gp10 family phage protein	A0A1L6BY07	Clostridium_phage	1.8e-16	34.3
WP_042188669.1|3668606_3668933_-	hypothetical protein	NA	NA	NA	NA
WP_042188672.1|3668929_3669316_-	hypothetical protein	NA	NA	NA	NA
WP_042193994.1|3669293_3669599_-	hypothetical protein	NA	NA	NA	NA
WP_042188674.1|3669598_3670546_-	xkdg	H7BVA6	unidentified_phage	2.8e-34	32.0
WP_042188676.1|3670567_3671794_-|terminase	terminase	A0A1B1P7E4	Bacillus_phage	1.2e-53	41.8
WP_042188678.1|3672353_3673436_-	DUF4179 domain-containing protein	NA	NA	NA	NA
WP_052404309.1|3673432_3673963_-	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_042188680.1|3674413_3675244_-	phage mu protein f	I6R1H0	Marinomonas_phage	4.0e-13	44.6
WP_042188682.1|3675236_3676715_-|portal	phage portal protein	A5GYL6	Lactococcus_phage	4.0e-48	30.5
WP_042188684.1|3676718_3678035_-|terminase	PBSX family phage terminase large subunit	E5DV50	Deep-sea_thermophilic_phage	1.7e-138	58.7
WP_081951135.1|3678021_3678927_-|terminase	terminase	D2IZ21	Enterococcus_phage	1.1e-32	39.8
WP_042188685.1|3679033_3679678_+	DUF4145 domain-containing protein	M1PSB6	Streptococcus_phage	6.7e-32	37.3
WP_042188687.1|3679674_3679884_-	hypothetical protein	NA	NA	NA	NA
WP_042188689.1|3680080_3681208_-	hypothetical protein	NA	NA	NA	NA
WP_042188690.1|3682333_3682870_-	transcriptional regulator	A0A1B1P7B5	Bacillus_phage	6.1e-47	50.0
WP_156113123.1|3683070_3683427_-	hypothetical protein	NA	NA	NA	NA
WP_156113124.1|3683548_3683704_-	hypothetical protein	NA	NA	NA	NA
WP_081951286.1|3683875_3684487_-	restriction endonuclease	NA	NA	NA	NA
WP_052404310.1|3684924_3686013_+	RelA/SpoT domain-containing protein	NA	NA	NA	NA
WP_042188695.1|3686132_3686624_-	hypothetical protein	NA	NA	NA	NA
WP_042188697.1|3686716_3686998_-	hypothetical protein	NA	NA	NA	NA
WP_042188699.1|3687183_3687567_+	hypothetical protein	NA	NA	NA	NA
WP_042188701.1|3687691_3688282_-	HNH endonuclease	A0A1S5SBA6	Streptococcus_phage	4.0e-31	40.1
WP_042188703.1|3688285_3688516_-	hypothetical protein	A0A2H4JCC5	uncultured_Caudovirales_phage	7.4e-18	63.5
WP_156113125.1|3688655_3688943_+	hypothetical protein	NA	NA	NA	NA
WP_042188707.1|3688974_3689406_-	hypothetical protein	NA	NA	NA	NA
WP_042188709.1|3689410_3689593_-	IDEAL domain-containing protein	NA	NA	NA	NA
WP_052404311.1|3689625_3690456_-	hypothetical protein	NA	NA	NA	NA
WP_081951287.1|3690478_3690643_-	RusA family crossover junction endodeoxyribonuclease	S6B1L9	Thermus_phage	5.1e-13	68.8
WP_081951136.1|3690611_3691307_+	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_052404313.1|3691324_3692488_+|integrase	site-specific integrase	M1NRJ9	Streptococcus_phage	9.6e-21	27.5
3696291:3696305	attR	NA	NA	NA	NA

Sequences of DBSCAN-SWA_6

Nucleotide sequences of DBSCAN-SWA_6

>NZ_CP009279|4730786:4738854|DBSCAN-SWA
CTTACTTGGAACTTTCACCCAATTTAAATAACGCCTTCAGTGCACTCCCTATAGCCTGAAACCAATTATCAGCAGGATAAGTGTGTGCTTGCGTTGTACTGTATTTTTTAGTATAAGCGGATTCCTCAGGTGGTAAGGACTCTCGTGTATATACTGGAACCCGGCCTATCTCCTTGCCACCTAGATCAAGAACGAGAACCCCTTGTAATCCAAAGTTTGATCTTGCAGCTTTGGCTGACGCCGAAGGGATCTGATTTAAGACAAGTTTGGTGGTCACTCTATCCTGCTCCCCTTGTCCGAGTGGATAGGCGAATTTTTTGGCTGTCACGAAGTCATAACCGCTCACGGGGTCCCCGCGTTCGATCATTGTTTTTAGTGGGTAGTGATTAAATCCAAAGTTTAGCAGTGAGGCATGATCATTCCAGTCATCCCCATCATTTATGGTCACTGCGACAAGCTGCTGGCCGTTTCTGGTCGCTGAGCTGACAAGGCAGCGTAGCGCTTTTTTGGTATATCCTGTCTTCACACCATCTGCGCCCTCATATAAGTACAGCATTTTATTTTTGTTTCTCCACTTGTAATCCCATTTCTCATTTGGATTGTCCGCAGTTTTCTCCTGTGTCTTCACAATTTGCTTAAATACAGGATTATGAAGAGCATACGCCGTCAGTACGGCTAAGTCGTTAGCACTCGAATAATGGCCTTCAGCATCTAGACCATGCGGATTAGCAAAATGAGTGTTTTTTAATCCGAGCTCTTCAGCCTTATTGTTCATCAGGTATACAAACCCTTCTTCAGAACCGCCGATATGTTCAGCGATCGCTGTTGCCGCATCATTCCCAGAGCGCAGCATTAGACCATACAGCATATTTTCCAGCGTCATCTCTTCACCTTGCTGTAAATAAATAGAGGAGCCTTCTTTGGCGAAAGCATTTTTACCAACTTTGACTTTGGATGCTAAATCACCATTCTCAATAGCGACGAGGGCGGTCATTATTTTAGTCAGGCTGGCAATAAGCATCGGCTCATCTCCTCGACTGCTATACAAAATACGCCCGGATTCCACATCAATCAGCGCCGCTGCCCGTGCATGCGTAGATATAGAGCTGTTCTCCGCATGAATCAAAGTTAGCGGTGTCAGAAACAGCAGCAAAATGCTCAGTAATAAGGCGATTGGAAATTTACGGGTTATTGTCTTCATATTTATCCTCCGGATTCTTATCGGTTCTTAAGTAAAGTCATTCATTTCATGCTTATGTTGTACAAGTGTATGCGGACCAGCCTTAGGGTATGTCCTCTCCACACAAAAAGGGACACCGCCTGATGTAAGGCGATATCCCCGAGGCTATTTGAACAATTATGTGTACCTAATGTGTTGAAGATTGGGATGTACTTGGATCGGGTTTAGCAGGTGCTTGTGATGCAGGTGCTTGTGGTGCTTGTGGTGCTTGTGGTGCTTGTGGTGCTTGTGTAGCAGTTGACCCAGCTTGACCTGAAGTACTGCTGCTTTGGAACATGGTCTGGATTTTGTCGATGAGCCCAGGCGTAGCATCGATAATTTTTTCGAACAAATGCGTTTGATTGTCGAGTGGAACAATGTTTACCCCATCTTTACCAACCACTAGAAAAGCGATCGGTCTGATGGAGACACCGCCCCCACTACCGCCACCAAAAGGAAGCATTTTGACACCGCCTTGGGAGCTTGATCCACTTATAGAATCCTCTACTCGATAATCACTACCCCCTGCAGCAAATCCAAAGGCCACCTTACTAATCGGTAGAATAATACTACCGTCAGGTGTTTGTACTGGATCTCCAACAATCGTATTAACATCTACCATGCCCTTGATATTTTCCATCGCTGTTTGCATTAGACCCTGAATAGGATGGTCGCTCATATTGTTTCCTCCTTAATTGAGTACGATTTCTCTTGCTTCTACAGCGCTTATCATCCCCACATCCACGCATTTGTATGTAACTTTCATTCTAAACTTTGCCCATGAGACTCCCTACGCATCCGTTTTAGTATTTTTCTCCACTTACTGATTCCCCCCGCCTCCCTCAAGACACGAAGAAGAAGCTGCAATGATGCGTATACGGCATAGGAAACGGACAATTTACCCTCACATACGAACTCCATTGAAAAAGAATGCTCATCTTGAAAAACAGGCTTCACAAACACTCGTGGATTGTGTTTCAATTTGACCCTCTGCGAAATAAATCCAACGATGCTCCATTTCAATCCCCAGACGGCTCCTGATACTATGGCAGTGTCTGCCGCATCACCTAGTGAGAAGTCTGTGGACCAGTCGAGCTTTGATATTTTGACATGTGATACAGTTTCCTTGAACCACTTCTTCAATCCACGTGTGGATTTCACTGCTAGCTGTACATTGTCCCGCCAGCGCTCAATTCTTTCTTTATCGAATTGTTCTTCCTTTACAGTGTCAACACCTGTAGTCGCGGTACCCGTCTCTTTAAACTTCCCAAGCACGCCTTGCTCCAATCCCTTAAAGACCAATCGAGGCAGTTCATAGTGCAGTTTGATCAGACCAAAAAGTGTCTTAACATCTAACTCGATCAGATCATTTTTGTCATGTTTATAGCACCGGATGCGGAAATCGATAGATGAAGACAGAACCAGGATCATTGCCAGTACCAGCAATCCGAGGGGTATTCCAAGCCATAACGTCACGTATTTACCTCCAAGAAACCTTAATAATGGGAACCTTTGGTTTAGTATGGCAATTTAATCTGGAAAAAATTCGGGGTTTGACTAAAAAATGTGGCTCTACAAAAAAATAGGGACTGCCCATAAACCATTATGAATGGTTTATGGGCAGTCCCAGCAATACAAATCATTGCGGAATAACAAAAAAACTAAGGTTGCTCTATATCCTCGAACGTCATTTGAGTATCCAGCTTATTGAACAATAGCTGTGTCTCCTCTTCCAAATTATCAGTGGATTCGAAGTTAGATGGTTCTGGCAGCTCATTCAGACTTGCTAGGCCAAAGCTCTCCAAGAATGATTTAGTCGTCCCATATAAGATTGGACGCCCTACGGCCTCCGCACGACCTACCTCATGGATCAAATCCTTGTTATTCAGCGTATGAATAGCACGTTCGGATTTCACGCCTCGAATCTCTTCGATCTCCACCCGTGTAATGGGCTGACGATAGGCCACGATCGCCAATGTCTCTAATGCGGCCTGAGACAAGGTTGATCTGGATGGGGAGTAAGCTAAGCGCTCAAAATAATGGGCATGCTCCGGCAATGTAGCCAACCGATAATTCCCGGCAATTTGGACTACCTGCAATCCCCGCTCCTGTGTTACATAATCCTCTTTTAGTTCTTCTAATGCTCCAGCCGCAAGCTCTGGCCGCTGCTCCGTAATCTCGGCGACTTGCCGTACGGAGATCCCTTCATCACCTGATAGAAACAACAGGCCCTCAATAATCGATTTCAGCGTTTTGTAATCCATTGAAGTGTTCTCCTCCTCTCCACTCCATTACGATGTCCTCAAACAATTTCTCCTGATAGCAAAAAATCGCCTTCATTTTCATCAGTTCCAGAATCGCAAGAAAAGTAACTACGATTTCGTGTCGCGCCATTTCATCGTGAAGCAGTGCTGAGAAGTGGAGCCTACCGCCCTTCCCTCTGCGCTGCAGCGCATCCGATACATCACGTATACGATCTTTTACCGATATTTCGTCCCGGGTGATCCGCTGGTAAGATGACCTTCTTGCCGCCTTACTAAGTGCTTTACGGAAAGCAGCTATAAGGTCGGAAGTATGTAGTCCTTTTAGCGTATGGTCAATCTCTTCAGGCACGTATGGACCCAGATCCTCCGGCTCCTTCGTAAAAATCAAGCTCCGCTCGCTCTCCATATCCATTAAATGAACAGCAATACTCTTGAATTTACGATACTCAATCAGTCGCTGAACAAGTTCAGCTCGTGGATCAAATTCATCTTCTTCGTAATATTCAAAATCATCGATCTCAATGACCGGTGGTTTGGGCAGCAATAGCTTGCTCTTTATAGATAATAGGGTTGCGGCCATCACGAGAAATTCACTCGTAATATCCAGTTCAAGCTCCTGCATACTTCGCAGGTATTCCATATACTGTTCGGTGATCTCGGCGACCGGAATGTCCTGGATGTCGATTTCCGCCTTATCAATTAAATGCAAAAGCAGATCCAGCGGACCTTCAAACGTTTCCAGCTTGTACAATACAGTCACGAAGCATCCTCCCGCCAAAAAAAGTAAAGTGCAGCGCCCTAAAGGACGCTACACAAGTAGAAAGGGCTCTATAATCCATGCTTTCTTCTTATACTATAAATAAGCACGAATTCGACTGATTCGTCAATAGCTGACTTACTTAAACAGTTTGTTAAGATTCGCCATTTCAATCGCAGCAGTCGCAGCATCCCAGCCTTTATTCCCTGCTTTGGTTCCTGAACGCTCAATGGCCTGTTCAATATTCTCAGTAGTTACTACGCCAAAAATCGTCGGCACGCCGGTTTTAAGATTGATCGCAGCTACCCCTTTTGCAACTTCATTACATACATAATCATAGTGCGTTGTAGACCCACGGATAACAGTTCCTAAAGTGATTACAGCGTCGTATTTACCGCTTTCCGCCATTTTTTGAGCGATTAACGGAATTTCAAACACGCCTGGAACCCAAGCAACATCTACTTCATCATCGTTAGCACCGTGGCGTTTAAATGCATCAAGTGCACCTGACAAAAGCTTGCTGGTAATAAATTCATTAAAACGTCCTACTACGACTCCGTATTTTAACCCCTCGGAAACTAAATGTCCTTCTAAATATTTCGGCATATCATTCATCTACCCTTCGTTTTTTATTGTGTGTGATTATACTTTCGAATCCTCATTTTGTTCAATGTCGTCAAAAGACAGCAAATGCCCAAGTTTCGCCTGCTTCGTATGGAGATAATTAGTATTATCCTTATTCTCCGGCATTTGAATTGGCACTCGCTCAACAACTTCCAATCCATAACCTTCCAACCCTTTGATCTTTCGAGGATTGTTCGTTAAGAGACGAATTTGACTTATACCTAGATCCTTCAGAATTTGTGCTCCAATCCCGTAATCACGCAAATCTGCTGGAAAACCAAGCTTTAGATTGGCATCTACAGTATCGAGTCCTTCTTCTTGAAGCTTGTAGGCTTTAAGCTTATTAATAAGACCAATGCCCCTGCCTTCTTGACGCATATAGAGCAACACGCCTCTACCAGCAGCTTCGATCTGCCGAAGCGCTGCTTCAAACTGGGGACCACAATCGCAGCGATGGGAGTGGAAAACGTCACCGGTTAAGCATTCGGAATGTACTCGTACTAACACTGGCTCATCACCGGAAATATCGCCCTTCACCAATGCTACATGTTCTTTATCATCCACTTCATTTGTATAGGCAATGGTCTGAAACTCACCGAAATCAGTAGGCAGACGTACAGACACCTCGCGATTGACGAGCTGTTCCTTCTCATTCCGATAGTGAATGAGGTCTTTGATGCTGATCAACTTAAGATCATGCTTCTTAGCAATCTCAACCAGATCAGGCAACCGGGCCATCGAGCCATCTTCATTGATGATTTCACAAATCACACTGGCTGGATATGCACCACACATACGGGCTAAATCAACAGCAGCCTCTGTATGTCCGGAACGGCGTAGTACGCCACCTTTTTTCGCAATCAGCGGGAACATATGGCCAGGTCTACGGAAATCAGACGGCTTCGCTTTAGGGTCAATCATGGCCTTTACAGTCAAGGATCTTTCCCCTGCTGATATACCAGTAGTTGTATCTATATGGTCAACCGATACAGTAAAGGCTGTGCCGTGATTATCTGTATTGTGACTGACCATAGCCTGTAGTTCAAGCTCTTCCGCACGCTCAGCGGTAATTGGCATGCAGACCAAACCACGTCCCTCAGTGATCATAAAATTGATGACTTCTGGTGTCGCCCGTTCAGCAAGAGCTATAAAATCCCCTTCATTCTCACGATCTTCATCATCCACCACGATAATGACTTTGCCGCGCATTAAATCATATATCGCTTCTTCAATCGGATCCAAGACACTATCCTTCTTCGATTGTTCGCTCATGATCCTATCCTCCCAATAGCTTTACGAAGGATTATTCCCTTCTTCGTAAGCTTACTCATTATTTAAACAAATCCGTTTGCCGCCAAGAAATCACGACTAATCCCGGAACTGCTATCACTTTCTTCATCCTGTGCAGCTGAGCCATAATGAAGAAGATGATCTACATATTTGCCCAGGACATCACACTCAATATTCACACTATCTCCTGCCCGCTTATAAGTTAGCACAGTTTCCCCTAACGTATGCGGAATAATGGATACAGTAAGCGATGAAGCCGTCGTCTTTACTACTGTTAAGCTAATGCCATCAATCGTGATCGACCCTTTAGGGATGATATATTTAAACAGCGATTTGCGATCCGGCGCAATCTCATAGACTACTGCATTTTGATCACGCTTTACACTTTTGATGACAGCAGTGCCATCTACATGTCCCTGAACAATATGACCTCCAAATCGACCACCGGCTGCCATTGCTCGCTCCAGATTCATCCGACTGCCAGGACGTAGCTCCTTCAGATTACTGTTTCGATAGGTCTGAGGCATGACATCCACTGTAAAATAGTTCTCGCCTAAAGCTGTCGCTGTAAGACAGACGCCATTAACCGATACGCTATCACCAATCTTCAAATCATCCATGATGACGGAAGCGGCAATGTTCAGCACCATCATTTCTCCACCGGTGGAGACACTTCTCAGAGTGCCAACTTCTTCGACTAATCCAGTGAACATGCTTTCCCTCCTAGGAGTTTTGTGTGAGTAACACTTCTCCGCTATCTCTCCGAACAAAACTTGCTCCGGAAGCACACGATTGAGTTTTGTAACCATTCACTTTAGCGTACCGGAGTACCGCTGATACATACATTATCTCCGAGCACTTTTACTTCCAATCCCTCCAGAGAAATCGCATCCTTCATTAGCTCTATACCAGGAAATACGAACGTCCCTTTCGCTTCAGCACCACCGCCAACAATCTTTGGAGCGAAAAAGAGAATCACTCGATCAACTAGCCCACTCTCCAGCATCGCACCATTTAGCGTGCCTCCGCCTTCAAGTAAAATCGATCCGATTTCCATTTCACCGAGTGTTACCATAGCAGCCTTCAAATCCACCCGTGGTCCTGCTCCGCTAACAATGATTTGCACACCTGCTTGAAGAAGTGCTGCTTTCTTTTCATCATCTGCGGCTTCAGTTGTCACGATGATAGTAGGCGCTAGACCGTCACTTACAACTGCTGAATCCAAAGGAATACGTAGTCCAGAATCAATCACAATCCGTATCGGATGAATACCCGGCACTTCCGTTCTTGTAGTCAGTGAAGGATTATCTGCAATCACTGTGTTCACACCGACCATTATTCCCTGATGCCGATGCCGCAGCGTATGTACGATCTCCCGCGCTTCACCATTTGAAATCCATTTACTGTCACCAGATTTGGTAGCTAGGTTACCATCCAGCGTGCTGGCACTCTTGAGCGTAACAAAAGGCTGTTTTGTCAAAATATACTTGATAAAACGCTCATTCAACCGCAGCGCACGTTCACGCAGCAACCCTACTTCTACTTCAATGCCATGCTCACGCAGCATTTGAACGCCGCGACCCGCAACCTGAGGGTTAGGGTCTTCACAAGCGACTACCACTCTGGCTACTCCCTCGTCGATCAGCCTTTGGCTGCAGGGCGGAGTCTTGCCATAGTGACTGCAAGGTTCCAGTGTTACGTAGGCAGTGCTGCCCTGTGCTTGACCGGCCGCCATATTCAAGGCATGAACCTCAGCATGACCTGTTCCGCGCTGCAAATGAGTTCCAAGTCCAATCATCGCTCCATTCTTTACAACAACACAGCCAACAACAGGGTTAATTCCTGTCTGTCCTTGGGCCCGTTCTGCCATATCCAGCGCTAACGACATATAAAACTCGTCATTCATATTATCCAT

Protein sequences of DBSCAN-SWA_6

>NZ_CP009279|4730786:4738854|4736983_4737652_-|WP_042190280.1|DBSCAN-SWA
MFTGLVEEVGTLRSVSTGGEMMVLNIAASVIMDDLKIGDSVSVNGVCLTATALGENYFTVDVMPQTYRNSNLKELRPGSRMNLERAMAAGGRFGGHIVQGHVDGTAVIKSVKRDQNAVVYEIAPDRKSLFKYIIPKGSITIDGISLTVVKTTASSLTVSIIPHTLGETVLTYKRAGDSVNIECDVLGKYVDHLLHYGSAAQDEESDSSSGISRDFLAANGFV
>NZ_CP009279|4730786:4738854|4737753_4738854_-|WP_042190282.1|DBSCAN-SWA
MDNMNDEFYMSLALDMAERAQGQTGINPVVGCVVVKNGAMIGLGTHLQRGTGHAEVHALNMAAGQAQGSTAYVTLEPCSHYGKTPPCSQRLIDEGVARVVVACEDPNPQVAGRGVQMLREHGIEVEVGLLRERALRLNERFIKYILTKQPFVTLKSASTLDGNLATKSGDSKWISNGEAREIVHTLRHRHQGIMVGVNTVIADNPSLTTRTEVPGIHPIRIVIDSGLRIPLDSAVVSDGLAPTIIVTTEAADDEKKAALLQAGVQIIVSGAGPRVDLKAAMVTLGEMEIGSILLEGGGTLNGAMLESGLVDRVILFFAPKIVGGGAEAKGTFVFPGIELMKDAISLEGLEVKVLGDNVCISGTPVR
>NZ_CP009279|4730786:4738854|4734236_4735028_-|WP_042190275.1|DBSCAN-SWA
MTVLYKLETFEGPLDLLLHLIDKAEIDIQDIPVAEITEQYMEYLRSMQELELDITSEFLVMAATLLSIKSKLLLPKPPVIEIDDFEYYEEDEFDPRAELVQRLIEYRKFKSIAVHLMDMESERSLIFTKEPEDLGPYVPEEIDHTLKGLHTSDLIAAFRKALSKAARRSSYQRITRDEISVKDRIRDVSDALQRRGKGGRLHFSALLHDEMARHEIVVTFLAILELMKMKAIFCYQEKLFEDIVMEWRGGEHFNGLQNAEIDY
>NZ_CP009279|4730786:4738854|4735163_4735631_-|WP_042194286.1|DBSCAN-SWA
MPKYLEGHLVSEGLKYGVVVGRFNEFITSKLLSGALDAFKRHGANDDEVDVAWVPGVFEIPLIAQKMAESGKYDAVITLGTVIRGSTTHYDYVCNEVAKGVAAINLKTGVPTIFGVVTTENIEQAIERSGTKAGNKGWDAATAAIEMANLNKLFK
>NZ_CP009279|4730786:4738854|4732152_4732683_-|WP_081951173.1|DBSCAN-SWA
MSDHPIQGLMQTAMENIKGMVDVNTIVGDPVQTPDGSIILPISKVAFGFAAGGSDYRVEDSISGSSSQGGVKMLPFGGGSGGGVSIRPIAFLVVGKDGVNIVPLDNQTHLFEKIIDATPGLIDKIQTMFQSSSTSGQAGSTATQAPQAPQAPQAPQAPASQAPAKPDPSTSQSSTH
>NZ_CP009279|4730786:4738854|4730786_4731986_-|WP_042190269.1|DBSCAN-SWA
MKTITRKFPIALLLSILLLFLTPLTLIHAENSSISTHARAAALIDVESGRILYSSRGDEPMLIASLTKIMTALVAIENGDLASKVKVGKNAFAKEGSSIYLQQGEEMTLENMLYGLMLRSGNDAATAIAEHIGGSEEGFVYLMNNKAEELGLKNTHFANPHGLDAEGHYSSANDLAVLTAYALHNPVFKQIVKTQEKTADNPNEKWDYKWRNKNKMLYLYEGADGVKTGYTKKALRCLVSSATRNGQQLVAVTINDGDDWNDHASLLNFGFNHYPLKTMIERGDPVSGYDFVTAKKFAYPLGQGEQDRVTTKLVLNQIPSASAKAARSNFGLQGVLVLDLGGKEIGRVPVYTRESLPPEESAYTKKYSTTQAHTYPADNWFQAIGSALKALFKLGESSK
>NZ_CP009279|4730786:4738854|4732766_4733480_-|WP_042190271.1|DBSCAN-SWA
MTLWLGIPLGLLVLAMILVLSSSIDFRIRCYKHDKNDLIELDVKTLFGLIKLHYELPRLVFKGLEQGVLGKFKETGTATTGVDTVKEEQFDKERIERWRDNVQLAVKSTRGLKKWFKETVSHVKISKLDWSTDFSLGDAADTAIVSGAVWGLKWSIVGFISQRVKLKHNPRVFVKPVFQDEHSFSMEFVCEGKLSVSYAVYASLQLLLRVLREAGGISKWRKILKRMRRESHGQSLE
>NZ_CP009279|4730786:4738854|4735667_4736921_-|WP_042190277.1|DBSCAN-SWA
MSEQSKKDSVLDPIEEAIYDLMRGKVIIVVDDEDRENEGDFIALAERATPEVINFMITEGRGLVCMPITAERAEELELQAMVSHNTDNHGTAFTVSVDHIDTTTGISAGERSLTVKAMIDPKAKPSDFRRPGHMFPLIAKKGGVLRRSGHTEAAVDLARMCGAYPASVICEIINEDGSMARLPDLVEIAKKHDLKLISIKDLIHYRNEKEQLVNREVSVRLPTDFGEFQTIAYTNEVDDKEHVALVKGDISGDEPVLVRVHSECLTGDVFHSHRCDCGPQFEAALRQIEAAGRGVLLYMRQEGRGIGLINKLKAYKLQEEGLDTVDANLKLGFPADLRDYGIGAQILKDLGISQIRLLTNNPRKIKGLEGYGLEVVERVPIQMPENKDNTNYLHTKQAKLGHLLSFDDIEQNEDSKV
>NZ_CP009279|4730786:4738854|4733665_4734268_-|WP_042190273.1|DBSCAN-SWA
MDYKTLKSIIEGLLFLSGDEGISVRQVAEITEQRPELAAGALEELKEDYVTQERGLQVVQIAGNYRLATLPEHAHYFERLAYSPSRSTLSQAALETLAIVAYRQPITRVEIEEIRGVKSERAIHTLNNKDLIHEVGRAEAVGRPILYGTTKSFLESFGLASLNELPEPSNFESTDNLEEETQLLFNKLDTQMTFEDIEQP

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042190269.1|4730786_4731986_-	D-alanyl-D-alanine carboxypeptidase	B6DZZ7	Stx2-converting_phage	8.4e-28	35.0
WP_081951173.1|4732152_4732683_-	sporulation protein YtfJ	NA	NA	NA	NA
WP_042190271.1|4732766_4733480_-	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_042190273.1|4733665_4734268_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	4.5e-14	31.3
WP_042190275.1|4734236_4735028_-	segregation and condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	4.9e-08	36.8
WP_042194286.1|4735163_4735631_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	9.5e-44	58.0
WP_042190277.1|4735667_4736921_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	3.1e-118	53.7
WP_042190280.1|4736983_4737652_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	5.2e-35	41.0
WP_042190282.1|4737753_4738854_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	2.3e-56	37.2

Sequences of DBSCAN-SWA_7

Nucleotide sequences of DBSCAN-SWA_7

>NZ_CP009279|5298678:5309522|DBSCAN-SWA
TCTAAACCAGTGCCTGACCCAGCTCATCCAGCTTCACGGTGCGTTGCTCCCCTGTATTCATCGACTTCACGGTAATTACACCATTCTTCAGCTCATCTTCGCCAAGAATCGCAGTATAACGTGCCGACATACGGTCTGCGGATTTCATCTGTGCCTTCATTTTCCGGCCTAGGTAGTCACGTTCTGCTGAGAACCCTTGGCTGCGCAGAATATATAGCTGCTTAGAGATTTCGATATCAGCTTCCTCACCGAGAGCTACGAAGTACACATCCAGTGGCTTCGCCGTCTCCAGCTCTACCTTCTGATCCTCCAAAATGAGGAGAATTCGTTCAAGTCCAATCCCAAAACCAATACCCGGTTGATCCGGTCCACCAATTTCTTCAACCAAACCGTTGTAACGGCCTCCGCCGCCCACGGTATCAATCGAACCAATACCTGCTGCTTTATATTCAAACGCTGTATGCGTGTAATAATCCAGTCCTCTTACAAGTCGAGGGTTAATGGTGAATTCCACACCCATGATATCAAGGTGCATCTTCACCTTTTCAAAATGAGTCGTGCACTCTTCGTCCAGACTATCCAAAATGGAAGGCGCATCTGTAAATTTATCTTGATCTACCTTACAATCCAGCACGCGAAGCGGATTACGCTCAATACGACGCTGACAGTCACTGCAAAGGGTATCCTTCATTGGTCTTAAGAAACCCAATAATTTCTCCCGATAAGCTGCACGGCTAGGTGCGTTACCGACAGAATTGATTTCCACTCTTACATCCTTAAGGCCAAGATCCTTATAGAATTGATAGCCTAAGGAGACTACTTCCGCATCAATAGCCGGATCCACAGCTCCAAAAGCCTCAATACCAAACTGATGGAATTGACGATATCTACCTGCCTGTGGACGCTCATAACGGAACATAGGTCCGATATAATACAGCTTACTTACATCAGGTTCACCGTAAAGCTTGTTCTGAACATAAGCTCTAACGACACCAGCCGTTCCTTCTGGACGCAGCGCCAGATCACGATCGCCTTTATCCTTGAACGTGTACATCTCGCCTTCTACAATATCCGTTGTTTCGCCTACTCCACGCTCGAATAACCCCGTATACTCGAACATCGGTGTACGGATTTCACGGTAATTGAAACGACGGCATAAATCTCTAGCCTTCCCCTCAATATACTGCCATTTCTCCACAGCTCCCGGAAGCACATCCTGCGTTCCTGTAGGTTTCTCGAATCTTTCTTTAGCCACAGTCTATCCCTCCTAAAAAATACCCCTCTAAATCTGCTCTCTTCATCACTTCATCATGCTAAACAAAACAAAAAATCCCCCGCCCTGTTTATAAAAAACAGGGACGAGGGATTATCATAACCAATAATACACCCGTGGTACCACCCACATTCCGGATCAGAACCATTCTGAATCCGCTCAAAGCGGTTAACGCCCGCCTACGCATAACGGCTACTGATAGCGGCAATATACATTGCCCACTTTCGCCGTACGTTCTCGGGGAGGTCATTCATTCGCTCATCAACAGAATCCTTGCAGCCAAGCAGAAACGATAGATCATCCATTGTACTGGATATCATCTGAATCTACAGGGGATTCCTCTCTGGAGTTGTGGGTCCTCGAATTACTTGTTCCCGTCATCAAAACCATATGATAAAATCGTATATTTTTAAATTCTACTGAACTACTGCGCTAAAGTCAAGGCAGGAAATGCGAAGATGAATAAAAAATTCGACAACTTTCAACTTTTGACCTTTAACTTCAACCGTTACAAAAAAATGACCTGCAGCCAAATGCTGCAGGTCCATCATCATATATTATTAAAAAGGGGGTCATGCCTTTATTATAAACACGCTATATTAAGGAAACATGTATGTAATATTACGATTATATTACATTCATGAAAGCGGTTTATTTTAATAGATTGTTGTTAATCAAATTGCTCTACAAATGCTCCTTTGCCCCGAAGGGTCTCCACAACCTCATTATAATTCTCTTCTGCAACACTTAGGTCCATCACATAACGAAGTTCACTTAAATCCCCATCTTCGAGCTCTCCATCTGCTACATCCGCACTAACCTGGTCTTCATCCACGCTATAATGGGTCTCAGGCTCATCACGCGTTTCGGAGGCGGCAACACCTGGGGCCAACATAGCTCCAGCTGCCGGAGTGCTACCCGTTCCAAGCGTCCCTACTGTACCTGCGGCTAACGTCGTATTACTAAACGGAGCTATCGGAAACAGAATTCTACGATCTTCCCCAATAGGGTCCGTGAGTGGCCATACCTCCAAGCCATCTACCTTGTAACTAATCAATGCTATTTTAGCACCTTCTGCTTCATTTTCCGTTCTAAAATATGCTTGGATTTTTCTGGTCATTACCATTACCTCCTTTAGATTATAAGACTCAGTGTTATAAATTGCTATTGCAGGACCTTCAATATTTCACGAACGAAGGCAGGCTCATCTTTCGGGGTACGCGAAGTAATGTAATTACGATCAACTACCACTTCTTCATCTTTAAACTCCGCACCAGCGTTCACAACATCATCTTTCAACGGAGGATAACAGGTGATGGTACGTCCTTTAAGCAAGTCTGCACTGATCAGAATTTGGGGTCCGTGGCAAATAGAAGCGATAGGCTTACCAGCTTCGTTTGCTTCTTTCACAAACTTCAAAATATCTGCATTTTGCCGTAAATTTTCTGGGGAAGAACCTCCAGGAATTACTATCGCGTCATAACTACCTGCTTGAACGTCAGCTATAGCTTTATCGGTTGCGTAGGAGACTTCCTTCTTTTTGCCTAGTAAGGTCTCACCCTTCTTTAAACCAATAATGTCAGCTTGATGTCCTGCCTTTATAACTTCATCGTAAGGGACCTTCATCTCAGAATCTTCAAAATCATTAGCTAGTAAAAATGCAACATTACTCATGTGATAAGTTCTCCTCTCTGCTTGTGCAAATGAATAGGTACTTATTTATCTTTCTTGTCGTCTATTACCCTTCTCACAATGATTTCTAACCTCTAATCAGAAAATATCCCCGGTTAACCGCATCAAAAAGCCGCCTCCACCACCCATTTCAGGTACGCGGTAAGAGATTACGGCTTCTTCCTTTGATCACTTGAGATTCAATATCATCTTCCGTCTTTTTGGCTAATGCATAGGCTTCTACAGGACTCCCTGTCGCTAGTGCCGGGATACTTCTCCATACCCATGCCTTCTGTGAATGTCTCATTACTAAGCTCCTTGCATCGTGCGAGATAACTGTCTACCTTTAGTTTATCCAGCTCCAAGAGGCTCTATCCGCGCAAGTATCTTACTCACAGCTCATCCACAATAAAAAAAGATGTCGAAAGTTAGCTCCGCTAGAAGCAATTTTCGACATCTTTTTTTTCATTAACTGCGGCTATCTAAAATGAGAGTAACCGGGCCCCAATTGGTCAGCGACACATCCATCATCGCTCCAAAAATACCCGTCTCCACTTGAAGGCCTCCAGCTCTAAGCTCTTGGTTAAAGTAATCATAAAGTCGTTCGGCCTCCGCGGGAGCTGCTGCTCCCATGAAATTCGGCCGTCTCCCCTTACGACAATCCCCGTATAAAGTAAACTGGGATACTGAAAGAATTGCTCCCTCAGTCTCTGTGACACTGTAGTTCATTTTACCAGCATCATCTTCAAAAATTCGTAGTCCTGCTATTTTATCCGCCAAATATTTGGCATCCTTTTCTGTATCCTCATGCGTAACGCCAACTAGCAGCATTAAGCCTTTGCCAATTTCTCCGGTCACTGCCTTATCCACGGTTACTTTGGCGTCCTTACAACGCTGTACTACAACTCTCATCGTACTACTCCGCTCCTTGCCCTATTGCATGATCCGATTCACTGTATATACATCCTTGACTCGTTTCACTTTATCTACAACGGATTGCAGATGTTCCGTGTTACGAATGAGAATGGTCATATGAATCATTGCCATTTTATTCTTGTCAGAGCGCCCAGTGACTGCAGAAATGTTCGTTTTACTCTCGGAAACTGCCTGCAGCACTTCATTGAGCAGTCCATTACGATCATGACCTGTAATCTCAATATCCACACTGTAGTTTGCTTCCATCGTACCTTCCCATTCCACTTCAATCACCCTTGCTGCTTCTTCTCCGTCACCTTCACTCGGAATGTTAGGACAATCCTGGCGATGTACAGATACACCCCGGCCCCGTGTAACATACCCTACAATGTCGTCACCCGGTACCGGATTACAACATCGTGCAAAACGGACAAGTAAATTTTCAATTCCCTTTACACTAACACCATTGGTCGGTTGATTACGTTTTTCGCCGGAAGACTTGATCTCCTTCATCTCTGAAGTAAGCTCTAAATGATTAGCAGCTTCTTCCTGCTCTTTGCGCAGCTTTTCCGTCAGACGGGAAGCAATCTGCGAAGCGGTAATCCCACCAAATCCAACAGCAGATAGCATATCCTCAACATCGTTAAAAGCAAATTTCTTCGCTGCTTCTAAAAGCTTATCATCAGAAATCCATTCAGAAACCTCGACATTCAGACGCTTCAGCTCACGTTCAATCGCTTCGCGACCTTTTTCGACATTTTCCTCACGTTTTTCTTTTTTGAACCATTGCTTAATTTTGCTTCGCGCATGTGAGGATTGAGCAATCTTGAGCCAGTCGCGGCTTGGTCCGTACGAATGCTTCGATGTCAGTATCTCTACAATATCGCCCGTCTTCAACTTGTGATCCAACGGTACGATCCGCCCATTCACCTTAGAACCAATCGTACGATTACCCACTTCCGTATGAATACGGAATGCAAAATCAAGTGGTACAGAACCCGCAGGAAGCTCAATAACCTCGCCTTTAGGCGTAAACACGAACACAAGATCCGAGAAAAAGTCCATTTTGAGTGATTTTACGAACTCTTCGGCATCCTTGGCCTCATGCTGAAGCTCCAATATTTCGCGAAAAAAAGGCATCCGATTCTCAGGATTCACATTATTGCTGGTTCCTTCTTTGTATGCCCAGTGTGCTGCTATCCCGAATTCAGCCGTGCGATGCATTTCCCAAGTGCGAATTTGCACTTCGGTTGGCTCTCCGCCAGGACCTACCACTGTAGTATGCAAAGATTGATACATATTGGCTTTGGGCATAGCTATATAATCTTTAAATCGACCTGGCATTGGCTTCCAAAGGGTATGAATAATTCCGAGGGTTGCATAACAATCCTTGATATTATCCACAATGATACGGATGGCCAGCAGGTCATAGATCTCATTAAACTGTTTGTTTTTCGTACTCATTTTGTTATAGACACTGTAGATATGCTTCGGACGACCTGAAAGATCACCTTCAATGCCCATTTCATCCAGCTTGGCACGAATACGGCCAATTACGCTGTCGATAAATTGCTCACGTTCAGCCCGCTTCTTATGCACTAGATTAGCAATGCGATAATACTGCTGCGGATTCAAGTAACGAAGCGCAATATCCTCCATCTCCCACTTAATCGCGGAAATCCCCAAACGATCAGCTACAGGACAGAAAATCTCCAGCGTTTCATAAGAAATACGTCGCTGGCTCTCTTCAGATTGATACTTTAACGTACGCATATTATGCAGGCGATCCGCTAGTTTGATAACGATGACCCGGATATCCTGCGCCATCGCAATAAACATCTTACGGTAATTCTCGTTCTGCTGCTCTTCCTTTGAGCGAAAACGGATGCGTTCCAGCTTAGTTAAGCCATCGACAAGCATCGCGCAGGTATCGCCAAATTTCGCGCGGATTTGTTCCAATGAGACCGTCGTATCTTCCACAACATCATGCAAAAGCGCCGCAACAATAGATATAACATCCATTTGCATATTGACGACAATATCTGCCACCGCCAGCGGATGCAGAATGTATGGCTCCCCCGACTTGCGGATCTGCCCGTGATGAGCCTGATCGGCAAATTCATAAGCTTCCCGGATGCGGAGAAGATCTTTATCTTTTATATAGGCGCCAGCCTTATCAATTAATCGCTCTATGCCCATTCTCGTCGTATCCGTTTCCTTTCTATAATAAAATGAACCCGCAATCATTCTGAAATCTGCAGGTTCCAATCATTTCGCAAGCAACTTACGCTCTTGTTCAAAGTTGTCTATAATTATGACGCTTACGAGGGATTACGTCAACACTTGCCATCTCATGGTATTCAAGAAGTAAAAGTTATGAAAATCGGACAAATTAATAACACTTGTGAAAATGTTGTTGTAAAAATGTCCAGTTCTATTTAATCTAGTAAAGGCGGATTTTCGCTGGACAACATCATATCCATTAAGAAAGAGGAGTGAACTCCATTGCAACGCGAAATTCAAGTTAATGAAAAACTTCCATGGGGCCCCGGTTTTCTGTTAAGCCTACAGCATTTGTTCGCCATGTTTGGCAGTACAGTGCTAGTGCCTAACTTGTTCGGGGTTGACCCTGGCATGATTTTGCTGATGAACGGTATCGGCACACTGCTATACATTTGGATTTGCCGTGGTAAAATACCTGCCTACCTTGGCTCCAGCTTTGCATTTATCGCACCCGTATTATCAGTGCTTGCTGATCATAAAGATGATCATATGAAAGGGTACTCGCTTGCTTTGGGCGCTTTCATCATCACAGGTGTTATCTTTGTGCTCGTTGCTTTGATCATCCGTTATGCAGGAACAAAATGGATCGATGTTGTCTTCCCTCCAGCAGTAATGGGAGCTATCGTAGCAACGATCGGACTTGAACTTGTGCCTGTTGCCGCGCGAATGGCAGGACTTATTGCCCCTGAAGGTGTTGCAGTTGCAGACTGGACTCCAGATGGCAAAGCAATCACACTTTCTATGGTGACACTGGGCGTAACCGTAATTGGAGCTGTACTCTTCCGCGGTTTCCCAAAAATCATTCACATCCTCATCGGTATCGTAACTGGTTATGGTTTAGCTTATATTATGAAAATGGTGGATACCGCTGCAATATCTAATGCAAATTTTTTAGCGCACCCTACCATTGTTACTCCATCCTTCGATTGGAATGTAATCCTGACTATCATCCCAGTATCGCTAGTAGTAATCGTTGAACATATCGGACACTTACTTGTAACTAGCAATATTGTTGGCAGAGACTTGGCTAAAGATCCTGGACTTGACCGCTCCCTGATGGGGAACGGGATATCTACAATTATCTCCGGTTTTATCGGTTCTACTCCAAATACAACCTACGGTGAGAATATCGGGGTTATGGCATTAACTAAAGTTTATTCTGTATATGTGATCGGTGGCGCAGCAGTGATTGCAATTCTGCTATCGTTCTCAGGTACTTTTTCCTCCGTTATCGCTAATATCCCAACACCTGTAATGGGCGGCGTATCACTACTGTTGTTCGGTGTAATTGCCGCATCCGGTCTGCGAATCTTCGTAGAGCAAAAAGTTGATTTTTCCAAAGCCACTAACATGATTATGGCTACGTTGGTGCTTGTTGTCGGAATTAGTGGTACAACCCTTACTATGGGTAGCGTAAAACTCAGTGGTATGGCTCTAGCTACGATTGTTGGTATCGTTCTAGCCCTATTCTTCAAACTCATTGAAGTTCTTGGACTGTCTAATGAAGGTGGAGAAAGCGATAAAGCTGCTCACTAATTTATTTATGAATTAATAATTCAAAAAGACTGCTCCAGATCCATTTTATGGATTGGGCAGTCTTTTTTCGTATCTCTTTTGACCAAAAAATCGAAAAACAGCAACCCTCCGCTAGTAGTGACAGAGAATTGCTGTTGTTTGCACTTTTTCACATTATTCGATAAATAAATCCCGATTTATTTCCCGGGAAAAGACAAGTTTATCGTATTAATCTTCGTAATCAACTAATGTAATAACTTCAATTCCAGAAAGCTTATTACGTCCAGCAAGCTCAACCAATTCAATCAAAAACGCTGCGCCTACCACTTTACCACCAAGCTGCTCCACAAGGTTAACTGAAGTAGCTATAGTACCTCCTGTTGCTAACAAATCATCAGCAATCAATACATTTTGTCCAGGCTTAATGGCATCCGTGTGAACAGCAAGTGTGTCTTTACCATATTCAAGATCATATCCAACCTCGATAGTCTCATACGGCAGTTTACCACTCTTTCGAATCGGCACAAAGCCTACGCCCAATGCATAAGCAAGAGGTGCACCAACTACAAAACCACGTGCTTCCGGTCCAGCGATCACATCGATTTCTAAGTGGGATACAAGAGCTTTCAAGGCATCAATTGCCTGGCGATATGCATCACCGTCTTTTAACAAGGTGGTGATATCTTTAAAACTAATACCTTCTTTTGGGAAATCAGGAATCACGCGAATACTATCTTTAAAATCCAAATTTTTCATCTCCTAAAAGTTTTGTTAGCATATGCTACTTTGAGTCCGGTTCGACAAAACTTACTTCGTAAGCGTCTGCTTTGTTTTGTTTAGTGTCTTTATGATACGCCTAAACGGCGTGATAACATCCAATCCTGCAGTTCAGACAAGCTACCTTCCATGAAGTACTGCTCCATTTCCGCCATCTGCCCCAGTCTGACAAAATGTCTTGATGCTGTAAGGCTTTTAGCTGTAGGCTGCGTAATAAAGGTCACACTTCCGTGACTTCTTTCGATAAAATCCAGCTCCTCGAACACATCTAGCATATTACTAAGCATTCGAATACTTAATGAGGATTGTCGACTTAGCCGCAGCAGCACTTCATGTTCTGGCGTTGCAACAGCAGTGATCGAAGCCAGCAGTTTATAGAGTATTTTAAAATGATCCCGTGTCGGAATGATAAGTCGTTCTCGGCCATCCTTTATAGAATGCAATAACGCAATATTATCAGCATTAGGAAAAGCCTTCAGTAACGCGTCTAGTTGTTCAGGAGTCTCTGGCATATCCAGTAAACATAACAGTGAGACATGCCCTGATTCCTGAATCGAATCATCCTTAATAGCGGCGCTAATGCCAGCTTCTTTATCATATACCCAGAAGGACATTCCTATCAATTCAGTCTGTGAAGACATACGTCCACTCTGAAACACTGCTGCAGCACGATATGGGCCAGCACCGCTATAGGGAAGCAGCAGCTCTCTAATATGTGCAGCCTGCCGTACAGCGTCAGCAGCACCACGAAGATCAAATAATTGAGCATCCTGAACTGATAAATCCTGTAGCATCAACTGTGGTTTCCTCGAGCCATTCCATTCGTTGATCGACAGTTCAGCCAGCACATTGATCGGGGTGCCCACAGGGAGCAGCTTAGCCAAATCCCCTTTACCAAAAGCCAAGGCTTCGATCGTACTCTTACCCTGTTGCAAGACGATCTTCAAGTGTTTTCCGTCTTGCCCCATGGTGCGTGTCTCTTTCACTGTAGCCCCGCGAATGATGAACTTTGGCAATGGATTCGACATCCCGAAAGGTGCAAGCCTTTCCAATTCAAGCGCGGTCTGTAGGGACAAATCGGAAATCGACACTTCTGCATCAGCAGAAGTAACAGGAACGAAATGCTCCGGTGTTAACACAGTAGCAGCGTATTCATTTAATGCCGCAGCGAAGGCTTCTAAGCCGTCCCGATGCAGACTCATTCCCGCAGCTGCTGGATGACCACCGAAATGATCCATTAAGTTAGAACAAGAGGATAAGGCCGCATATATATCAAGTCCAGGAATAGAGCGGGCAGAACCTTTGCACATGCCGGTCTCCGGATGAATATCCAGAATAATTACAGGTCGATAGTAACGCTCCAGCAGTTTGGAAGCCACTATGCCTACCACACCCACATTCCAACCTTGTTCAGCAAGGACTATGATGTCTGGTATTTCTCCACCCTGAGTCATCTGCTCCAGTTTTGCAGTGGCCTCCACTACAATTCTTTCTACGACCAATTGGCGTTCTTTATTAAGCAGATCAAGCTCCCCAGCCAGTTGCTCTGCCTCATCAGTATGCTCGGTTGTAAGCAACGCCACTGCCCGTCCAGCATGATCCAGACGACCACTCGCATTGATACGAGGCGCCATTCCAAAAGCGATATTAACCGCGCTCACAGTACTCATGGTTACGCCGCTAACATCGAGTAAGGCACGAATACCTGGGAATCGAGAATTTCGCATACTCACCAAGCCGTTTCGAACAATCTCACGATTCTCACCCAGCAGCGGCATTAAATCCGCTACAGTACCGATAGCAGCTATCTCTGCCCATTCTTCGGGAGTTTCCTCCCCTAGCATAGCCTGGGCGAGCTTATAAGCTACACCTACACCTGCCAATCCTTTGAACGGGTAGGGGCAGTCGGGCAGCTTCGGATTAATCAACGTATAAGCCTCTGGGAGAAGCTCTGGTGGCTCATGGTGATCCGTAACAATCACATCAATCCCGAGTTCATTAGCGTAAGCAATCTGATGATAGGCGCTAATGCCAGTATCTACAGTAATGATCAAGGATACACCCTGCTGTAAAGCCCAATCCAAAGCATGATTATGCAGCCCATAGCCCTCATTAGAACGGTGCGGGATATAAATATCAAAGGAAGCGCCTAAGTAACGCAGCAAATGAATCATTAATGCTGTACTGGACACACCATCGGCGTCGTAATCACCGTAAATCAGAATATGTTCTTCTTCTTTTAAAGCCTTTCTAATTCTGGGAACCGCTTCGGCCATTCCTTTTAGAAGGAACGGATCATGCGGAGCTTCCACACCGCCATCCATGAACGATAGAGCCTCATGTGGCGTATCAATTCCTCTAGTCACTAATAGTGAGGATAAGAGCGGAGAAATAGAAAGGCTCCGGGCCAT

Protein sequences of DBSCAN-SWA_7

>NZ_CP009279|5298678:5309522|5298678_5299932_-|WP_042191091.1|tRNA|DBSCAN-SWA
MAKERFEKPTGTQDVLPGAVEKWQYIEGKARDLCRRFNYREIRTPMFEYTGLFERGVGETTDIVEGEMYTFKDKGDRDLALRPEGTAGVVRAYVQNKLYGEPDVSKLYYIGPMFRYERPQAGRYRQFHQFGIEAFGAVDPAIDAEVVSLGYQFYKDLGLKDVRVEINSVGNAPSRAAYREKLLGFLRPMKDTLCSDCQRRIERNPLRVLDCKVDQDKFTDAPSILDSLDEECTTHFEKVKMHLDIMGVEFTINPRLVRGLDYYTHTAFEYKAAGIGSIDTVGGGGRYNGLVEEIGGPDQPGIGFGIGLERILLILEDQKVELETAKPLDVYFVALGEEADIEISKQLYILRSQGFSAERDYLGRKMKAQMKSADRMSARYTAILGEDELKNGVITVKSMNTGEQRTVKLDELGQALV
>NZ_CP009279|5298678:5309522|5302089_5302533_-|WP_042191098.1|tRNA|DBSCAN-SWA
MRVVVQRCKDAKVTVDKAVTGEIGKGLMLLVGVTHEDTEKDAKYLADKIAGLRIFEDDAGKMNYSVTETEGAILSVSQFTLYGDCRKGRRPNFMGAAAPAEAERLYDYFNQELRAGGLQVETGIFGAMMDVSLTNWGPVTLILDSRS
>NZ_CP009279|5298678:5309522|5305041_5306355_+|WP_042191101.1|DBSCAN-SWA
MQREIQVNEKLPWGPGFLLSLQHLFAMFGSTVLVPNLFGVDPGMILLMNGIGTLLYIWICRGKIPAYLGSSFAFIAPVLSVLADHKDDHMKGYSLALGAFIITGVIFVLVALIIRYAGTKWIDVVFPPAVMGAIVATIGLELVPVAARMAGLIAPEGVAVADWTPDGKAITLSMVTLGVTVIGAVLFRGFPKIIHILIGIVTGYGLAYIMKMVDTAAISNANFLAHPTIVTPSFDWNVILTIIPVSLVVIVEHIGHLLVTSNIVGRDLAKDPGLDRSLMGNGISTIISGFIGSTPNTTYGENIGVMALTKVYSVYVIGGAAVIAILLSFSGTFSSVIANIPTPVMGGVSLLLFGVIAASGLRIFVEQKVDFSKATNMIMATLVLVVGISGTTLTMGSVKLSGMALATIVGIVLALFFKLIEVLGLSNEGGESDKAAH
>NZ_CP009279|5298678:5309522|5307179_5309522_-|WP_156113244.1|DBSCAN-SWA
MARSLSISPLLSSLLVTRGIDTPHEALSFMDGGVEAPHDPFLLKGMAEAVPRIRKALKEEEHILIYGDYDADGVSSTALMIHLLRYLGASFDIYIPHRSNEGYGLHNHALDWALQQGVSLIITVDTGISAYHQIAYANELGIDVIVTDHHEPPELLPEAYTLINPKLPDCPYPFKGLAGVGVAYKLAQAMLGEETPEEWAEIAAIGTVADLMPLLGENREIVRNGLVSMRNSRFPGIRALLDVSGVTMSTVSAVNIAFGMAPRINASGRLDHAGRAVALLTTEHTDEAEQLAGELDLLNKERQLVVERIVVEATAKLEQMTQGGEIPDIIVLAEQGWNVGVVGIVASKLLERYYRPVIILDIHPETGMCKGSARSIPGLDIYAALSSCSNLMDHFGGHPAAAGMSLHRDGLEAFAAALNEYAATVLTPEHFVPVTSADAEVSISDLSLQTALELERLAPFGMSNPLPKFIIRGATVKETRTMGQDGKHLKIVLQQGKSTIEALAFGKGDLAKLLPVGTPINVLAELSINEWNGSRKPQLMLQDLSVQDAQLFDLRGAADAVRQAAHIRELLLPYSGAGPYRAAAVFQSGRMSSQTELIGMSFWVYDKEAGISAAIKDDSIQESGHVSLLCLLDMPETPEQLDALLKAFPNADNIALLHSIKDGRERLIIPTRDHFKILYKLLASITAVATPEHEVLLRLSRQSSLSIRMLSNMLDVFEELDFIERSHGSVTFITQPTAKSLTASRHFVRLGQMAEMEQYFMEGSLSELQDWMLSRRLGVS
>NZ_CP009279|5298678:5309522|5306562_5307081_-|WP_042191103.1|DBSCAN-SWA
MDFKDSIRVIPDFPKEGISFKDITTLLKDGDAYRQAIDALKALVSHLEIDVIAGPEARGFVVGAPLAYALGVGFVPIRKSGKLPYETIEVGYDLEYGKDTLAVHTDAIKPGQNVLIADDLLATGGTIATSVNLVEQLGGKVVGAAFLIELVELAGRNKLSGIEVITLVDYED
>NZ_CP009279|5298678:5309522|5300620_5301070_-|WP_042191093.1|DBSCAN-SWA
MTRKIQAYFRTENEAEGAKIALISYKVDGLEVWPLTDPIGEDRRILFPIAPFSNTTLAAGTVGTLGTGSTPAAGAMLAPGVAASETRDEPETHYSVDEDQVSADVADGELEDGDLSELRYVMDLSVAEENYNEVVETLRGKGAFVEQFD
>NZ_CP009279|5298678:5309522|5301114_5301624_-|WP_042191095.1|DBSCAN-SWA
MSNVAFLLANDFEDSEMKVPYDEVIKAGHQADIIGLKKGETLLGKKKEVSYATDKAIADVQAGSYDAIVIPGGSSPENLRQNADILKFVKEANEAGKPIASICHGPQILISADLLKGRTITCYPPLKDDVVNAGAEFKDEEVVVDRNYITSRTPKDEPAFVREILKVLQ
>NZ_CP009279|5298678:5309522|5300366_5300504_-|WP_156113175.1|DBSCAN-SWA
MMMDLQHLAAGHFFVTVEVKGQKLKVVEFFIHLRISCLDFSAVVQ
>NZ_CP009279|5298678:5309522|5302554_5304735_-|WP_042194390.1|DBSCAN-SWA
MGIERLIDKAGAYIKDKDLLRIREAYEFADQAHHGQIRKSGEPYILHPLAVADIVVNMQMDVISIVAALLHDVVEDTTVSLEQIRAKFGDTCAMLVDGLTKLERIRFRSKEEQQNENYRKMFIAMAQDIRVIVIKLADRLHNMRTLKYQSEESQRRISYETLEIFCPVADRLGISAIKWEMEDIALRYLNPQQYYRIANLVHKKRAEREQFIDSVIGRIRAKLDEMGIEGDLSGRPKHIYSVYNKMSTKNKQFNEIYDLLAIRIIVDNIKDCYATLGIIHTLWKPMPGRFKDYIAMPKANMYQSLHTTVVGPGGEPTEVQIRTWEMHRTAEFGIAAHWAYKEGTSNNVNPENRMPFFREILELQHEAKDAEEFVKSLKMDFFSDLVFVFTPKGEVIELPAGSVPLDFAFRIHTEVGNRTIGSKVNGRIVPLDHKLKTGDIVEILTSKHSYGPSRDWLKIAQSSHARSKIKQWFKKEKREENVEKGREAIERELKRLNVEVSEWISDDKLLEAAKKFAFNDVEDMLSAVGFGGITASQIASRLTEKLRKEQEEAANHLELTSEMKEIKSSGEKRNQPTNGVSVKGIENLLVRFARCCNPVPGDDIVGYVTRGRGVSVHRQDCPNIPSEGDGEEAARVIEVEWEGTMEANYSVDIEITGHDRNGLLNEVLQAVSESKTNISAVTGRSDKNKMAMIHMTILIRNTEHLQSVVDKVKRVKDVYTVNRIMQ
>NZ_CP009279|5298678:5309522|5301772_5301928_-|WP_156113176.1|DBSCAN-SWA
MRHSQKAWVWRSIPALATGSPVEAYALAKKTEDDIESQVIKGRSRNLLPRT

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042191091.1|5298678_5299932_-|tRNA	histidine--tRNA ligase	A0A1V0SFH3	Hokovirus	7.7e-16	23.6
WP_156113175.1|5300366_5300504_-	hypothetical protein	NA	NA	NA	NA
WP_042191093.1|5300620_5301070_-	hypothetical protein	NA	NA	NA	NA
WP_042191095.1|5301114_5301624_-	type 1 glutamine amidotransferase	A0A0N7KVR4	Yellowstone_lake_phycodnavirus	4.5e-23	41.8
WP_156113176.1|5301772_5301928_-	hypothetical protein	NA	NA	NA	NA
WP_042191098.1|5302089_5302533_-|tRNA	D-tyrosyl-tRNA(Tyr) deacylase	NA	NA	NA	NA
WP_042194390.1|5302554_5304735_-	bifunctional (p)ppGpp synthetase/guanosine-3',5'-bis(diphosphate) 3'-pyrophosphohydrolase	J9Q7H7	Salmonella_phage	2.2e-10	40.0
WP_042191101.1|5305041_5306355_+	uracil permease	Q9KX94	Enterobacteria_phage	9.7e-70	38.3
WP_042191103.1|5306562_5307081_-	adenine phosphoribosyltransferase	A0A1V0SKE5	Klosneuvirus	2.3e-27	44.4
WP_156113244.1|5307179_5309522_-	single-stranded-DNA-specific exonuclease RecJ	A7KV88	Bacillus_phage	6.4e-80	33.5

Sequences of DBSCAN-SWA_8

Nucleotide sequences of DBSCAN-SWA_8

>NZ_CP009279|6056248:6072755|DBSCAN-SWA
CTTAGTGAGTACTTTTAATCTCAACCGTTCTAGTGGCGGAATCATAACCCACCTGTGCACCTAGCGCTTCTGCAATAATACGAACGGGAACGTAGGTGATGCCTTTTTCAAGCACTCCATCTGCAATCTTAACCCCGTTAACCTTTACGACGGCAATAACATCACTCTTCAAGTCTTCCTCCTCCTTCCGATGGATGATTTTGTACGCTGCCTCCACTGCGGATGTTGAGGGCTTGCCCCCTGCACGTAACTGTGTGAGCGTTAACCCAAAAGCCATTTGAAAATGTGGGTAATCCTTAAAGCTAGTCCAATCGCCTCCCCATTCGAATCCAAGTGCCTTGGCCTCTTTTACAACCTCCTGCCAATCTGCGATCTGGTTGTTATTGTCGTCCCGGCGCATATCCCAAGACACACTCGATCCATTCGGCAGCAAAAGAGCAAAATCTACGGCTAGTCCAAAATTGTGGTAGCTATACCCGCCACGCGCATTGGTAACAATCGCTCCAGGCTTAGTGCGTCCTTGTGCGTAAAGAGCATCCTGCTCAGCAATTGTGCGAAGACCCTGCGTAATGAGAATGGGGATGTTGAGCTTGTAGCAACGCTCGATTAGAGCAGTAGCAGCGGAACGGACTACGGGGTGTAGACCTGTTAGGCGTGAGGCTGATTTATTTTTTACCTGCATTAGTGTCAACATGATGATCCTCTTTTCTGTCTATCTTTTTCAGATAAATAAATTGGTCATATTTCCCGGAACGGGTCAATATTGCGAGTATGATGATCCCACCAGTTGTACCGAAATGGGCGATAGCCCAGCTATATTGCAGCCAAATTAGCCATGCTGCCGAGTCCGCTCCTAGTAGAGCTACCAAACGGAATAGTAGAATGATTAACATATTGAATGTATGGGCCATTAAGAAAAAAAGCATAGCCAGCATAAACACGCTGACCACACCTTTTCGGAATCGTTCATAAAAATATTGCCTGTGGCGATAAATGATATATAATCCGCAGGCTGCAGTAGTGCTATATAGCAACAATAATAAAAAATCAATCATGTGCATCATGATCCCCTCGATCATAGACTAAATATTTGGCGAATCGGTTACGATCAATCTCCTCCTGAATTTCCTGCGAGACATTTTTATAATGACTTATGGTCAGCGTAACGCTGGTAGAGGCTCTGCGGAGCTCCATCTCTTTATCAACATGCCGGGGGAGAAGCAGCCGCCGAATCCATTGTGACAGCATTCCTAACTCCCCCTGTCTTCCGTATGGTCAATCTTCAGTTTCTTTAAGACGTCCAGTGTCGGCTGCATAAACTCCGAGCGCTCCTTGTCCAGAATCGCTTGCAGACGATCCCGATCCTCCTCTGCACGATCCAGCAGTTCTCGCGGTACAAGGTGTTCCCTTTGACAATCGCACGCAATAATACCATGAGCACGATCATCAAAATAAACGCAACAATATAAGCCAGCCCATACTTATCCGCCAGCGGCAGCAGCTTCTCCAATTGCGCAATATCCCCCTCTTTCATTCGTCCGCTCCTTTCTGTAATGATGTTGATGCAAGATAGCCCCCGGCACACCGAGGGCACAAAAAAACACGCTCCTGTGTGGGCGTGCTAGTTACTTAGCTGATGCTGCTTGCTCGGTCGTATTATTTTCAGCAAAATGAATATCTGATCGCTTCTCCATAATCTGTGCCCTAACCAAAATCTGATTGTCAGCCTGCATGTTATATGATGAGATGATATCCTCTATAGGACCTTCCTCACGATCGTAACGAGTCATGCAGGCATTAGCCATCAAGCGGATTTTGGCGGCTGTTAATGAATCCATAGTCATAGTGTATGAACCTCCTAGTAGTATTAGATGCTTAGTAGTTCAGCAATAATGACTTCAACGTCTTGAAGACGATCCTGCAAAGCAGTATTTTCTACGCGCAGTTGTTCGACTTCGCTTAATTCTGGCGGTTTGTTAGCTTCTGCTTCTAGGTACGCTTGCCACGCTGCTTCGAGTTCTTCTTCTGTAGGTTGTGGGGCGTCTAGGTTCCAGGCGGCGATGTATGGACCGCGTTCAATAATGTCGTAGTCTTTGCCTTCGACTAGTCGATTAAAATCCACTGCATAACGATAGTGTACCCCTTCTATTAACTTGGATTCATCTTCTTCTAATGGGCGGATCTCGTAGCGTATGTGACCATCTACGCCTTCGCGTAATACAGGTTCAGGACCGTCATCCCGCACCATAAAGTCATGCACTGGGTCAGATTTTGGGTGCATGTGCATAATTGCTGCTGATATGTTCATTATAATTCCTCCATTACGCAATTTGAGATACCTTGAATCTTGAATATATAGAATCAGTCGTTATGCTTTTATCTATAGAATTATGATGCTGCACATAGGCTTCAAGTTTGTCTCCGGCATTTATAAGGAGCATAGCAGTTAAAGATAGCTGTATGTCGCCACCAGAGTTCACTGGTATACCATAAGTACCTATTTCTCTGTTTGTTCCGTTTCTATAAATTTGGAGGTAATGAGAAGTTAGTGCTTCCGGCGAACTAACTACAATAGAACATTCAATTAGATAAAGCCCTGATTTCGCTGCTGTAAACATACTCGTCGAAGGGTTATATTCACCGAGATTGTCGTAATACTCAGTTTGGAAATTAATCTTTGTTAAAATAGCTTTCGGAACCACTTGATTAGTAGATGGTATGGCAGAAAAGGCACTTCGTTTTGAAAATGTATTATCTCCCCAAGGGTTAAGAACTCCACTAGTGATGATACCATTTAATGAGCCTTCGGAAGTTATTCCTGATGGCTGTGAGCCATATTTATAGATTGAACCGCCATGACTAGCGTAAAGACCCACGCCATTCGCTTGCCCCGTGTTATCGAGTGATGTAACAATCGAAGCACTTCCGACTATTATTCCAAAGTTTCGTCCAGATACCGAAGAATTTCTAATGTCTGCGTTTTGACCTGCAATATTAATGCCCGGATAATTAGCGGTAGTTTCACAGGAGCAATTTTTAATGTCGATGTTTCCGCCGTCATACGCATTAAAACCCATTGAGGTTGTGGTATTAGCAGAAAAACCGTCTATAACAATACGATTGCACCGTTCAGCCACGAAGGAGCGGATAGTTACAGAAGTACCCATAAATTGAACATGACCACCGCCTACTTTGCCGCTTATTCTCACATCTTCGGCATAGGTTCCAGATGCAACATTTATAGATGCAGTATGATTAACAACTTGAGGAATCATGCCGATAGCCCTATTGATTGTTTTAAATGCCCCTGCTGCCGTATTGGCTGAACCGTTGTTTGTGTCGTTCCCATCCGTCCGCACATAGTAAGTAATATCAGCCGTCGTCTGCTGCGGTGTAGTAACCAAAGGCGCCTTACCATTCAACTGCCCCTGAATCCCACTAGTCACCCCATCCAAATACCCAAACTCTGCGTTCGAGACCACGCCAGTCCCAATCTTCGAAGCATCAATCCCAGCCGCAGAATTAACGTCTGCATTTACAATCACTCCAGTCGCAATAGCCGTAACTCCATCACCATTACTAGTAACATCCCCCGTGTGATTAGGATGCACATAATTATTCGCTCCCGTAGCAATACCCGCCAGCTTAGTTTTCTCAGCTGCGGTGTAATCGTTGGTCGACAGCTGTTTGCCAGTAACTTTATCGACCTTGCTAGTAACGGCATTATCCAAGATGTCCATATTCCCATTTAAATCGGCAATATCAACGATATCTGTTCCCTCGGGCTTCTTTAATCCCAAATTTCCTGTGGTTTGCATGTGTCACTCTCCTATCTATAAGTTCTTAATTCATTCCATGTTTTACTGTGGGCATTCTCCCAGTTTAAAACCTTAACAGAGTCCCACCAGGTATAGCTGAACACAAATTCATAAGCTAAATGCGCGGGTTTAATCTCTTCAATAATTTGAATTAGCCCTGCCATATTCGGAGGGATCCCCAGCGTACTCACAAAATGAATCTCAAAACGGTACTCATCAGGCACTTCCTTAACTTCAACCACTCCACCTGAAAAAGCGGACGCTGTCCGCTGGATCATCTCCGGCGTTGTCGTCCCGTTTCCACGCAGCTTCGCCTTAATCATCTCTCGGCGTGTGGCATATGACTTGGATGAATCAATATTTAGTCCAAGCTCAGCCTCCCAACGTCCAAGGCTCACCGTTGCTGTTTCAACAAACGCCTGATCCAGTACATCTATAGTACCTACCTTCAGTCCACCAATTTCTAGCCCGATGGTCTCCTGAAGCTTCTCCATTTCACGAACATTCTTATAATAATCCGGCAAATACTGCATTAGATCAGGCGCTTCGACTTCACCCGGATGGCTCGAATCTTTATCTGCCGAATATTGCAATTCGCTGTATAAAGAGCTGCCGTAACTCATCCTCTACACCCCCTTCAGTTGATTCCAGGTTAGGGGGCCTTTGGGCAAATAATCATGTGTATGCGCCGCCGGAGGGAATACCGCTGGTTTACCCGCTACACCCGCCCAAGCTACACTATCCGCTTGTTGCGCGAAATCCACCTTGCCATTGTTATTCGTATCGTAAATGCTTTTCAGCATATCTCCGGTACTCTGCGCGGCTACCAGTAAGACATTACCAGCTGCAGAACCAATGTACAGCTTGCCACTGTCTGTACAATAGCCAAGCTCACCAATAGCCAGTGCTCCAATCGCACTTTCCAATCCGCGGCGTATTTGAATCAATGTCTTTAAAGCCATTGTCCCGCCCCCTAGAAAGTTCCGCCATCAATACTGGCTACGGTAAGTTTATTGCCATTCGCAGCATCATAAATGATGCTACTTCCATCCACACTTACAGCTACACCGGATCCATCTACGGTGATCCCTTTTCCAGCCGTCACCGCAATCGCGTCTGCAGTAACCGTGATCCCATTACCTGCACCAATATTCAGCGTCACAGCATCGGCTTGACCGCCGCCGATCAGCCCGTTACCAGCGGTAATAGTCTGTAACGCACCACCTGTGCGCACCCATGCGCTACCGTTCCAGCTATAAATCTTCTGCTCATCATCGACGTAAGCGGTCCAGCCTACAGCCGGAACATAAAATACCCAAGCGGCAGATTGATATTCAACGATTTGATTCGTTTTCCCCGCCCATGCCCCGGTTGCTCCAGCTGGAATAATGTATCGATCACCCTCAACCGGACTGGCTGGTGGAGCCAGCAGGTTCTGATCTTTTACCGACGCTTGCGGTTCAATGTTATGCTTGGCCAGCTCAATTTCATTTTTAATCTTTTGCGCTGACCACAAATCTGTAATCGTAGTCCCGGCATCATTGATCGTCCGGTGCTTGGTCACATCATCAATATGAGTCTTAATCTCAGCCGCGGTCTTTACGTTCGTGCCATCTGATACTTTATTGATATGCCCCGCACTAATATCCGCTTTAAGCACCTTCGCATAGGTTGCTCCATCAGCGATATCATCAATTGTACCTGTCAGATCGCTAAGCTTCTGCGCATTCATCCGCCGCCAGGCTGCCCCATCATCAAAATACAAATATCCGCTATTCGTACCCGTAGTCACGTAATACAAACGGCCAACGGCTCCTGCAACTGGACGAGAGGCTTCTGGACCCGATAGTGCCCTTCCGACCATGGAATTGGAAGTCCCATCACCAACATAAACTTCCTTAGTGTCACTGCAAAAACCAAGCTCTCCTACCTTCAACACGCCATAACTCGTTAGTTCAGCCTTTGTTCCCCGCTTTATTTGTATGGTCTGTGCCATTTTACACCTCTCTTCTAAAAGATCCCCCGTCAATCTGGCCCTTGCTCTTATAACGTTCTATTTCAGTTTGAACAGCAGTAAGACTTTCCTGCAAACCGTTAATATCCTCTGCTTCAACGGTATCGCCGGGGGTTTCGTAAGTCACATAAACCTCGGGCACATCGGCAAAAATCTTAATCAACCGCCGCCATGGCGCTTCATCCGGAAAAGACACCGTAAAATTACGCAGCTCGATCCCGGAATACTGTGACCCTGTGTACACTGCGATGGTCTGATTATTGATGTTGTCATGCGCAAGCGCACCACTATACATGCCATTTACAAGCGGTAATCTCTCTTCAATAACATAGCTGCCGCCGTTTGCTTTTTTATTAAGCTTTTCTTGAAAAATATCAACTTTCTCCGGATAACCCATGCTACACCTCCAGTAAAACATTGCCGAACAATGGAATTTCTTCTTCGTTCAACATTACGTTGCCCGCTCCACCGTTCAGCTTCAGCTCACTGTAATCTGCGACTCCCTCAGTAGCTAGCAATAGGGCACCGATTACAGACTGGCTAATATAGGTTGCTGAAAAAGCCTTCTCTTTGCGATAGCTCTCAAGAATCGCCTTAAATTCTTCATTTACAGCTTGCAGCGCATAACCTGAAGCAAGGGTTACTTTTGCGCTTACACTAATACTTTTGCCCTTCGCTGACGCCACAGTTACAACAGCACCTACGGGGGCTTTCCCCTCACCCGCTCCAGAGACCGGATCAATGTAATGCTGAACCTTTGTCACCAGCAGCTCAGAAGCAGGAAGTTTCTCGGCATCCACAACAATCACTTTCACCGTCTTAGGACCGTTCCATAACGGAAAAACACGTGCACCTCCCACCCCTACAACCTGCATAGCCCACTCCATATAGTGATATTTATTGCCGCTAGTAGCTGGGCGTCTGGCTGAATCCAAATAACGCTGCCGTAGCGATTCATCCGATTCGGAGTTCTCCCCAGGGATCAGAAGGGAAGCTATTTCCCCACGCGCGAGGTCTGAAATATAATCCACCGGCAGCAAAGAGCCAAAATATCGGTTTCCTTCTTCTCCAGCGGTTTCACTCTCCAACCGGTACACTCCAGGAGATAGCTTCTCCACAGCCATATAATTCAGCATATCGAGTGAAAAGCGGCTTCCGAGAGGGACATCTACAAATCCTCCATCCGCTTTATAAAAAATCCCCTTCAGTTGCGCTTTGCTCGCTTCTCGCCTAACAATTCCTGACCAGGATATACTTCGCTCCAAGTACTCTCCGGTCGCCGTATCTGCAAAATACAGATTATTATTCACATCCAGCTCAATGTACATCTGCGCGAGCTCTGCTGCTGCCGGAGCGAGCGCGTCATAAATAATGCTGCCCTCGCGTTTATCCAGACCTGACGGAACCCGGTCCAGCATCCGCTCTAAAAGAGCCTCATACGTCTGATTCTCATACATCCTCATTCCACTCCTTTCTCAGCTGAAAATTTCCGTAACGTGTAACCACCTTGCAGTCAAAAGTTAAGTTTTCTCCGGTAAAAGAAACCTCAATATTTTCTAAGCTAAGGATTCGTTCATCCTGAAGTAAGGCCTCATTAATGACACGTCTGATTTCAGCTCTGACTAACAGCCGATCCTTACCCAGAACCAGCTGCCACTCTGTTCCGTAATCCGAACTGTAAATCAGATGTTCAAATCTATCGGTTCGCAGAATTTTGGCCGCTGCCTGCTGCACTGCCTCAAGTCCATCCACTTGGCCAGTGATCCTTTTTCTGTCCCAATCCATTCGGTAAGTTAGACTGGGGCTTTCCCCACGTTCAAGGTTGACCTCGCCTTCAAGAAGGGCAGTTATCGGTCCAGATTTTCCAATCGCAGGAATCATATCGGACTCACCAGCCGATCCAGAACAATATAGCTTTGTCCACCCTGCATCCGAACCATCAGAACCCGATCACCAGAGGCAAGCCCTCGACGCACTACCACTTCTCTACCCTCTAGTTCGACTTTACATTCCATTACCGATTCAGGCAGCACTAGCGCATTCCCCGATAAAATAAAACGTTGATCCACCTGGATCTGCAAAGGAGCTACCTCCGTTACCGTCCCATAAGAAAAAGCCACGGGATTTGTATTTCCCACGGCTCCTAAGCTTGCTTTTTTTATAATATCCAACATCATTTCTACACCACCTTTATATCGAGGGACATCGTATGCTCCCCACCGGAAATCTTATGACTGCATTGATCCACCAGAAACACCTGAGTCTTGAATTCATCAAGCAGGACATAAATGAAATTACCAGCCCTTACGCGCATATCACCAATCGCCTGTACGGAGAGACTAAGCTTTTCACGGTTGTGCATTTTTAGCAGATTATTTGCCTTCTCCTGAATTTGTGCAGCATTCGCTTTGTCATCGGCCTTCTGATACAAGTGCAGGATACCCCAGCGTTTCACATTATCCTTATCGCTAACCGGAAAGAAATCACGCTTACCAGACTTCTCGTTATCCTTGTATAGAAAAATGGTGTTGTACGTATCATCATCAATACTTTTTTTGAGCGAATAGTCGTACAGATACTGCCCCGCTCCCAGCACCAGATTAAGCAGCATAGACTCCGGTTTACGAAGCGTCAGCTTACCAAAGTCATCGTAAAAAGCCATCAGCCTCCCCTTATACTGAAGCTCACTGCCGATCGCTCCCATAATGATGTCCAGCAGCTTTTTGTCATCTTGAATTAATGAGGGAATTCGGTACTCTGTATTCTCCAGCACACCTGTCTTCAGGCCGTAGTCCTTGGTTATTTTAGTAATAACATCGCTAGCCGTGACATCCTGCAAAACATAACTACCATTGCCTAGTAAATAACGAATCTGATCATAAGCAGTCAGCTTAATCTCCTGATCCGAGCCTGTATCAATGCTGAACACAAACCCGTAGAATACATCCACATTATCTTTGCTGAACTGAATAATATCACCGTTGTTGATGCTAAACTTGGGATGCTGATAGATTCCACTGTCCACAAGTGTTAACTCTAGCGTTGCTGGCTTTCCTGAGCGGGCTGTTTTCCAAGAAATATCGGAGACGATGCCAGAAATATCCCATAGATTCCCTTCCTTATTCTTCACAAGCAGTTCCATAACATCCTCCTACGGCAGCTTAATGACCTTACCGATTGGAAGCTTCCTCAGCTCACTATCTTTAATGCCATTAAGTTTCTGGATTTCTCCACACCTTTTGCCATCTCCAAGAATTTCTTTAGCGATTTTCCATAGATTGTCTTTAGATTTCATGATATACGTTTTAGGTTTGGGCTTTTCATTAGCCCGCTTCTGTTCTACCTTCACTTCATCTTTGACAACCTTAACTGCTACCGCTTGATAGAATACATACTTTTTGAGAGATAAAGAATATTCAATATCCCCTGATGTACCTGCACTGAGCTTCCAAGTGAAGCCTTCGATACTCATAGCCATATTCACACCAAAATCAATCTCTATGGATTTATCCTCACTAGTCGATGATTGCTTTAACCATTTCTTCGCATCGTTTAGCTTCCCCTCAGCTTTTTTCGTGTCATCCGCATAGCTCACCCCGGAGAATACAAAACGAATAGGCCTGCGACTCGTCATCCACTTCTTAATAAGCTCCACATATTCAAAGGGTCTCTTCAGCCCGTCCTCTTGTACCAATACGAACGGATATCTTTGTGCCGGAAATATACTTTCAATTGTGATCTCCGTCAGCTTCGGATAAGCAATCGTATTGATCTCACCCAAATCGATAATGGTATAGCTTTTTCCATCCCCGCTCTCTTTGATCTCTAAGGTCTCCGGGTTGACTGGCAGCCGGAATGCTTCCGCCTGATTATTAAAACCAAGAAAAATCCCGTACTCTTCCATGTTACGTATACACCCCCTGCGCTGTAGAGACAAACTCCTCGTTCAGCTTTTGCCCGATCTTGTTGATAATCGTATCAATGTCTCCGGCATTATTAATATTCCCGGTCGTCACCTGCACCGTCGGCGTAAGCTCCACAAAATTCTGGATCGCCTGAATCTCCGCTAGCTCACGCAGCATTTTCAGATCATCGCTAGAGATGTCTACAGTGTCGTTGATGGAGTCGAGTTGCTTCACGCGGTTTACGGTGTTTAGATTACCTGGAGTTCCTGCATTTTGAAAAGAACCCGTAGCTGAAGGTGTATTCATCGTAGGAACTACTGGAATTTCAGGTACGGTAGGCGTTTGCAAAGGTTTTGACAAATCCCCTGAATGGGTAGTATTCCACTGATTTAATGTGGTGTTATTACTCTTATTTCCACCTACATTTAATTTTTCTTTAAACTTATTGATATCAAAATTCTGGATTTTTTCTGCCCCTGAATTAAAAGAAGCTCCAATGTCCATTTGCAAATCCTTTTTGAATTGACTGCTATCAACCTCTTCAATATGAAGATTGATCTCCGACTCTATACCAATAAATTTGCCAACAGCTCCAACTACTTTATTTATACTATCTAGCAAAAAGTTCACAGCGCCAATAATACCATTAACAAATCCGGTCCAAAGATCGATAACAAAGCCCACAAATTCTGCAACGAGCTGTCCCAGTCCCCTGAACATATTCGCCAAAAAGTCCCTCACAGGCTGAAGGGCTGCCACAATCCCTAAAAATGCTACTATAAGTGCAACTATAAGCCCTATTACAAGTGCAATTGGATTAGCACTCATCACAGCGTTGAAAATGCCTTGGGCTGCGGTAGCAATTCCGGTAGCAATAGATGAAATTCTAGTTGCAATTGTTGAGGCATTCATCGCGATTGCTAAGGCAATAACTCCAGCAACAACACCCAAAACAATCGGCAAAACAACAGGGTTGCTAAGAACACTCCAGAGATACAATGCACCTTGTACGACCTGCGAGAATACTTGTGCAAGTATCGCCAGTCCAATCGCTATCCCATCGATAATTGGCTGAAAGCTTCCATCTGAAAATGCCTGGTTAAGAATGCCTAATAGTGGTGACAATGCCGCAAGAGCACCTTCTCCCATACCAGCCAGAGAGTTGTTATAGTTTCCAAGAAGAGCTTGCCATTGATTAACGGGTGAATCCATCATGGTTTGTAGCGAATCACTCGTCATCCCTGACGTTGTCATAATATCTCCCAAAGTACTCAAAAAGGCTTCCATATTGCCCGTTCCGGCCACTAGATCAAGTCCACCCAGATCCTCTTTATCCACCTGAAGCATGGATGCTAAATCACTAGAATCCCCCTCAAAAGCAGAAGTAATCGCCGATGAAGTATCACCAATATCTTTACCCTCCGGAGACATCATGCTTAGCCTTGTGGAATAATCCATAAGCTTATCTAACTGATCCGTATTTTGAGTTTTAGGATAAAACGACAAGACACTTTCCATGGACTTGTTTACATCCTGCCCGGTATCTAGTGCCCTCTTCTTGAACTTATCAAACATTGCCACACCAACATCAGCATTTCCGGTTTTCGCTTTAAAAAGATCCTCCCATTTTTGCTGTTCAGCTGCAGGCGCAAGCACCTTTTCCATAACTCCTTTAACTTTTTCCAGCACACCTTTGGCTTTCCCAAAAGCACCGGTGATCTTTTCCCATGTACCCGCCTGCTGCTCAGCACCTGTTGCTCCTTGTTCTGCCGCATCGTTCAGTCTCTCCTGAGCCTGTACTGCGCCTCCAATAGAAGCTTGAATCCTGGTATAAGCTGCACTGTAATTGTTAGTGATGTTGTACACGGGCTTATTGACTATTTTCATACTGATTCGGTTTAAAGTTGCGGAAAAGGAATTTGAAATATTTGCAGAAACCTGAGTTGTAATTTGATTGGTTATATCATTAATCCATTGATTGGAGACTTGCTGGATTCCAGCTATATTGTTTTGCATACCTGCCATTCATTCACCCCCTATCTCTTCCTCGCCTTACTCCGTGCCTGATCCCGCTTCTCCTTCTCCACCCGAACAGCAATCATCGCATAGATTGCGGCACGTTCGCGCGAAGACAGCTTCATCAGCTCATGCGGTAAAATGTGCAGCTCGTGGAGGGCGTAGTAAGCCAAGTTGGCTTCGCTGTCGCCCTCGTTGATTAGTTTTTTACTTCATCCACCAGCTCGTTCATATCTGTGCCGAAGCCATTCAAGGCTTGCACTCGTTCACCCAATGCCGCGAATTCACCCGGAAGCAGCATTTTTCGCAGCAGTGTTTCAGCACCAAGGACACCATAAGAACGCTGTAGCTCGGCATTTTTCAGATCCGGATGCACCACACTTGAAGTCATAAGCTTAGCCATATAATCATTCGGTTCAATCTCGGAGGTATACACTCCGTTCTTACCTTTGACCTTACGAGTAGCTGCTTTACGGCATTCCTGATTCTCATCCTCGTTCATACTGCGTAGCTTCCAGGCAACTGCGTTCCCTTCCTTATCCTTAAACCGCTGCGATACCACAAACTCCTCGGTCGTGTCACATGCTACATTTTGCGCAAAAAACAAACTTAATTCACTCATTGTCTTCCTCCTAAAATGATTTAGTTTCTTCTAGTACTACTAACTAGACAGAGAAGAGACCCGCCGCTCACCTGCACGCCCGGGCCTTACTTGCTCCTATCTAGTTGTCTTTATTAGTTTCCAGAGCCTGCTGGAGCGCCAAAAGCTTGCACAATCTGCACGTCTTCAAAGGTAAAGCTCACTTCTTCTTCCAGCGCATCTGATTCTGTATCAAGAGAAGCCATGATGACACTATCAAGGTTCACGCCTTTTAAAATAATGCGTTGTGCTCCCACACTGGACGATGGGTCTTCGTTCGTAACCTCAATATCGAAATACTGATCGACACCTGTGTTCATATAATCAAGCATCATCTGGCGGAAACGGCTAGTCATATAAAAAATCGTCATCGAACCGCTGCCCGACCATCCAGTCGCTTTATGCTGAACACCACGTCGGCCGAGTGTCTTCACTTCCGCCTTTGTTTTTTCTACCGTTGCTTCAAGCGTCTTCACATAGAACATCTCTTCAGCTTGCGTGCCAATCACGGCATACGCACGGCCCTCCTGGCCGGAAATCGTATCACTAGCCTTTAAAAATGCCATCTTAAACCACCTTCACTTTCATATATACTTTTTCTACGGAATCTACCGGTTTCACAGCCACATCCAGCACGATACTATCACTATCCGCACCAGCCACAACGACAACATCTGTCTGCGCGTTAAAGCCCTCAATCGCACCCATATCCTGCAGATCATTCATATAAGTCGCACATTGTGACCAGAACAGAGCCCGTCCATCTTCATTATTCGCTACCTTACCAATGTAGTAGTTCTCAAAAATACGCTTCAGATCATTCGCAATCCCATCCAGCACGCGTAGCACACGATTTTTGGAAAACGCTTTGCCTTTATCCGGAGAAAATGCCGTAAACGTGTTAATATCTTGCTCCACCACAGCTCGCCCTCCACTGTAAGTAAAGAGCAATTCACCTCGCAGCAAAGCTGCAGTCGTCTCAGAATGGCTAAGCCGCACATCAGCGTCAACGGAGTCGTCATATCCCTGATAAGTCAGCGATTGATTCACCGCAGCAGCAGCCGTAGCACCGGCCACCCAAGCAACAGCATTGTTATTATCAATCATAGTTCCGTCACTCAGTACTACCCCATTCTTCACGCTGATCACACCCTCATGACCCGCAGTAGCATAATCCGATAGTACAGCCTGTACTTTCTTCCCTTCAGTATCCCGCAGTCGTCTTACCCAAGAGCTATACAGCGCCTTAAGCGTACTATCCTGCGATACTAGTCCAACCGTTTGGAACTCAAGCACCTCAAGAGCAGACAAGAAATCGCTGTGCGCACCATTTGTCACCGTACCATTAGCTCCGCCAATAAGCGGCATCCCTGCGGTTAGCTTCAAGCCTTCTGCGCCATTTTTCTGGAATTGTACATAATCGTTAGCGACCAACTCTTCAGCCGTTCCAACCGTTTGCTTATTCAGTTCAGTTCCATTCAACAGTGTCTTTACATCAAAAAGAGCATTATTCTCAATATTCTTCTCAATAACAACAGAAAGATCATTTCCGCGTAGACCGCCATATTTAGCCGTAACCTGTAGACCATTGTTCGTGACCGCCGCTTTAACCCCTTCATTCAATCGATAGAGCAGTAACGTTCCCGCACGTTTCAGCGCTTCGCGTACTGGCAGTAATGTTGGGTGTTCCAAATCATAACCTAGCAGCTTATTCACGTCGTCCTGCGGGGTAATCTTCATGATCACTCCAGCTTCTCCCCAAGATAAGGCAAGTGCCAAAGCAGTAATCCCGCGTTCTCCCATTTTGCCGATGGCACCTTGATTCGATGCTACATTTACATACACCCCTGGGCGCACTTTGTTTTGAGTTGTCCATGTTCCGCCTGCCATTAGTTCAAAACCTCCTTATTCATAAACAATCCCATAGATTGCTTCGCTTCTTCGATCGTATAACTTTTGTCATCCTGCAAAATAACGTTCAGCACATCCTTTTCCTTAGCCGTAAAAAGCGATGAATTCACAATCTGCTCTTTACCAAAACGATCTCCATTACTCACCTTTGTGCTCATTTCAGTCTTTCTCCTCCTATCATATGTCCCATCTTAATGGGGTCAGGCTTCTCACTTTGCAAATACACCATATAGTCTGTTGTAAAAAGCGGTCCATGCCCCTCTACCCCAGCTTCCCAGGCTTGCCTAGCTACACGAAAGGAGCCACCCTCTTGCTCCATCCCTGCCATTGCCTCACTCAGCTTATCTGCCATTCTCTCAGCTTCCAGCAGACTGCCTTTTTCATAACGGATACCGAAGCGATAGACCGCTAAATATCGGCCTTCCCGCTGCCGATCCAGTGTCGCTGAGATCAGTCCGGGATAAAAATAAGCCGTCTGAGGTTTCTCCCCCTCCACATACACAGGCACATCTGGAAAATACCGCTCCAGCGCACTCGTAATGTGTTCTCGTAATTGTTGTACCGACATCACTCCATTCCTTTCTGAACTGCGGCGGTTCGCCGATCCTTGATGGTGTTAACCTTCAATTGCATTAACATTTAAGAAGACACCCCCTCTACTAAAATTAAGAACAAAAAGGATACTATCCAATGTTGGATAATACCCTTCTATACTAGGCCAATGCCAAAAGAATCTTTCACCGCTAGATTTGTTCTCATCACCACTAGGGTTGAACTATTAGCAGAGCATTCATGCTCTTGCGGTGTTCTTTTTGCTTCATTTGCCATGTTATAAATATACACCCCTATTTGCCTTGCAGAGACGGTATACCGACGAGGTTTAAGCTAGCTTTGGGATGGTATAGAGCGGTTTTTCGGAGGATCATAAAATCAATAAAAAAAGACCGCATCATCCGCTCGGACGACACAGTCTTTAGTAACCGTCTATATCTCTTAAGTAATACTAATCTTCTCTTTCTTCACTCTAGGTGCTGTTATTAAAGTGTTAAGGGACAGTAGACCGAGATCCGTTAAAGCCAAAGCCATCTTATAAAAAGCCTTCGAGCGTATCTTCACGTAAGTATCCTTACTTACCGGTGGATCAAACACATGATTGTAAATCGTATAATCGTACGTTTCGTCTCTTTTCATATAACGCTCTCTTACTAATTGCTGTTCCCTCGTATCGAGTCTTTCTACCACAGAGTCTATCGCCGAGCAAAAAGCCCTCCTAGCAGCCGGTATATCCACATTATAAGAAGCTATCGCAGCAGTCTGATCAGTAACAGTATTCGTAGGACCATGAAATCTTTCTGTATACGAATAAGTAGTACTGGCTTCCTTAGCCTCAAATGTAACGGTCTTAAAAATACGGTATTTCTCCAACATGCTCTCTATAGCGACCTGGGTTCGGCGACGGTCTAGCTCCGGTAAAGCAGATAAGTTCATCATTTTATGCACTCCTTTAGGTTTTAACAGAATGAGATTAAATTGCGGAAGTTTCCTAAGCAATGTGCTAAAATATAAAAGTGTTCGTATTCTGTTCGTATTTTTCTATAATATACCACTTCTCTACCAATCTCGTAAAACCCCGTTTGAGTCTGTTTTGGGCGAAAAAGAATAGCTTTCCCTCCATTATCTTGCCTTTTGGCAATAATATACGCTTTGTTGTTTACCAATTGGCAAAAATGGCTTATATTAATAACATAAGCTTCAGTCTATAAGGAGTGGTTGAGATGAAACAGGATTTTGGGGATTATATGAAGCAACTTCGCGAAACTAAGGGACTTACTATTAATCAATTGGCAGCAGCAGCAGGTATTAGCGGATCACAGATTTCACGGATTGAAAATGGTCTAAGAGGTGTTCCTAAGCCAACTACATTACGCAAAATAGCAGAGGCTACAGGAGTCCCGTACGAGGAGCTAATGGATCAAGCGGGGTATTTGCAGGAACAGGCTCTTCCAAGCGAAGAGATTGTCCCAGAGTGGGCTACAAGCAAGGATAAACGTGACTTCCGTAAAATGCTGGAGGATGATGGAGAGCTGATGTTTGATGGGATTCCACTAGACAAGGATGACAAACAGAGGATAAAAGATGTACTGACCGGCTTATTCTGGGAAGCCAAACAGATGAACAAGAGAAAGAAATCCAACAACACTTAA

Protein sequences of DBSCAN-SWA_8

>NZ_CP009279|6056248:6072755|6061038_6062061_-|WP_042192110.1|DBSCAN-SWA
MAQTIQIKRGTKAELTSYGVLKVGELGFCSDTKEVYVGDGTSNSMVGRALSGPEASRPVAGAVGRLYYVTTGTNSGYLYFDDGAAWRRMNAQKLSDLTGTIDDIADGATYAKVLKADISAGHINKVSDGTNVKTAAEIKTHIDDVTKHRTINDAGTTITDLWSAQKIKNEIELAKHNIEPQASVKDQNLLAPPASPVEGDRYIIPAGATGAWAGKTNQIVEYQSAAWVFYVPAVGWTAYVDDEQKIYSWNGSAWVRTGGALQTITAGNGLIGGGQADAVTLNIGAGNGITVTADAIAVTAGKGITVDGSGVAVSVDGSSIIYDAANGNKLTVASIDGGTF
>NZ_CP009279|6056248:6072755|6069207_6070530_-|WP_042192128.1|DBSCAN-SWA
MAGGTWTTQNKVRPGVYVNVASNQGAIGKMGERGITALALALSWGEAGVIMKITPQDDVNKLLGYDLEHPTLLPVREALKRAGTLLLYRLNEGVKAAVTNNGLQVTAKYGGLRGNDLSVVIEKNIENNALFDVKTLLNGTELNKQTVGTAEELVANDYVQFQKNGAEGLKLTAGMPLIGGANGTVTNGAHSDFLSALEVLEFQTVGLVSQDSTLKALYSSWVRRLRDTEGKKVQAVLSDYATAGHEGVISVKNGVVLSDGTMIDNNNAVAWVAGATAAAAVNQSLTYQGYDDSVDADVRLSHSETTAALLRGELLFTYSGGRAVVEQDINTFTAFSPDKGKAFSKNRVLRVLDGIANDLKRIFENYYIGKVANNEDGRALFWSQCATYMNDLQDMGAIEGFNAQTDVVVVAGADSDSIVLDVAVKPVDSVEKVYMKVKVV
>NZ_CP009279|6056248:6072755|6057872_6058091_-|WP_042192102.1|DBSCAN-SWA
MTMDSLTAAKIRLMANACMTRYDREEGPIEDIISSYNMQADNQILVRAQIMEKRSDIHFAENNTTEQAASAK
>NZ_CP009279|6056248:6072755|6065230_6065983_-|WP_042192121.1|DBSCAN-SWA
MEEYGIFLGFNNQAEAFRLPVNPETLEIKESGDGKSYTIIDLGEINTIAYPKLTEITIESIFPAQRYPFVLVQEDGLKRPFEYVELIKKWMTSRRPIRFVFSGVSYADDTKKAEGKLNDAKKWLKQSSTSEDKSIEIDFGVNMAMSIEGFTWKLSAGTSGDIEYSLSLKKYVFYQAVAVKVVKDEVKVEQKRANEKPKPKTYIMKSKDNLWKIAKEILGDGKRCGEIQKLNGIKDSELRKLPIGKVIKLP
>NZ_CP009279|6056248:6072755|6062477_6063536_-|WP_042192114.1|plate|DBSCAN-SWA
MYENQTYEALLERMLDRVPSGLDKREGSIIYDALAPAAAELAQMYIELDVNNNLYFADTATGEYLERSISWSGIVRREASKAQLKGIFYKADGGFVDVPLGSRFSLDMLNYMAVEKLSPGVYRLESETAGEEGNRYFGSLLPVDYISDLARGEIASLLIPGENSESDESLRQRYLDSARRPATSGNKYHYMEWAMQVVGVGGARVFPLWNGPKTVKVIVVDAEKLPASELLVTKVQHYIDPVSGAGEGKAPVGAVVTVASAKGKSISVSAKVTLASGYALQAVNEEFKAILESYRKEKAFSATYISQSVIGALLLATEGVADYSELKLNGGAGNVMLNEEEIPLFGNVLLEV
>NZ_CP009279|6056248:6072755|6058568_6060065_-|WP_042192106.1|DBSCAN-SWA
MQTTGNLGLKKPEGTDIVDIADLNGNMDILDNAVTSKVDKVTGKQLSTNDYTAAEKTKLAGIATGANNYVHPNHTGDVTSNGDGVTAIATGVIVNADVNSAAGIDASKIGTGVVSNAEFGYLDGVTSGIQGQLNGKAPLVTTPQQTTADITYYVRTDGNDTNNGSANTAAGAFKTINRAIGMIPQVVNHTASINVASGTYAEDVRISGKVGGGHVQFMGTSVTIRSFVAERCNRIVIDGFSANTTTSMGFNAYDGGNIDIKNCSCETTANYPGINIAGQNADIRNSSVSGRNFGIIVGSASIVTSLDNTGQANGVGLYASHGGSIYKYGSQPSGITSEGSLNGIITSGVLNPWGDNTFSKRSAFSAIPSTNQVVPKAILTKINFQTEYYDNLGEYNPSTSMFTAAKSGLYLIECSIVVSSPEALTSHYLQIYRNGTNREIGTYGIPVNSGGDIQLSLTAMLLINAGDKLEAYVQHHNSIDKSITTDSIYSRFKVSQIA
>NZ_CP009279|6056248:6072755|6056248_6056941_-|WP_052404439.1|DBSCAN-SWA
MLTLMQVKNKSASRLTGLHPVVRSAATALIERCYKLNIPILITQGLRTIAEQDALYAQGRTKPGAIVTNARGGYSYHNFGLAVDFALLLPNGSSVSWDMRRDDNNNQIADWQEVVKEAKALGFEWGGDWTSFKDYPHFQMAFGLTLTQLRAGGKPSTSAVEAAYKIIHRKEEEDLKSDVIAVVKVNGVKIADGVLEKGITYVPVRIIAEALGAQVGYDSATRTVEIKSTH
>NZ_CP009279|6056248:6072755|6062062_6062476_-|WP_042192112.1|DBSCAN-SWA
MGYPEKVDIFQEKLNKKANGGSYVIEERLPLVNGMYSGALAHDNINNQTIAVYTGSQYSGIELRNFTVSFPDEAPWRRLIKIFADVPEVYVTYETPGDTVEAEDINGLQESLTAVQTEIERYKSKGQIDGGSFRREV
>NZ_CP009279|6056248:6072755|6057538_6057781_-|WP_042192100.1|DBSCAN-SWA
MKEGDIAQLEKLLPLADKYGLAYIVAFILMIVLMVLLRAIVKGNTLYRENCWIVQRRIGIVCKRFWTRSARSLCSRHWTS
>NZ_CP009279|6056248:6072755|6057294_6057495_-|WP_036681274.1|DBSCAN-SWA
MLSQWIRRLLLPRHVDKEMELRRASTSVTLTISHYKNVSQEIQEEIDRNRFAKYLVYDRGDHDAHD
>NZ_CP009279|6056248:6072755|6056912_6057302_-|WP_042192098.1|DBSCAN-SWA
MIDFLLLLLYSTTAACGLYIIYRHRQYFYERFRKGVVSVFMLAMLFFLMAHTFNMLIILLFRLVALLGADSAAWLIWLQYSWAIAHFGTTGGIIILAILTRSGKYDQFIYLKKIDRKEDHHVDTNAGKK
>NZ_CP009279|6056248:6072755|6068020_6068200_-|WP_076120992.1|DBSCAN-SWA
MNEGDSEANLAYYALHELHILPHELMKLSSRERAAIYAMIAVRVEKEKRDQARSKARKR
>NZ_CP009279|6056248:6072755|6068735_6069206_-|WP_042192125.1|tail|DBSCAN-SWA
MAFLKASDTISGQEGRAYAVIGTQAEEMFYVKTLEATVEKTKAEVKTLGRRGVQHKATGWSGSGSMTIFYMTSRFRQMMLDYMNTGVDQYFDIEVTNEDPSSSVGAQRIILKGVNLDSVIMASLDTESDALEEEVSFTFEDVQIVQAFGAPAGSGN
>NZ_CP009279|6056248:6072755|6058114_6058555_-|WP_042192104.1|DBSCAN-SWA
MNISAAIMHMHPKSDPVHDFMVRDDGPEPVLREGVDGHIRYEIRPLEEDESKLIEGVHYRYAVDFNRLVEGKDYDIIERGPYIAAWNLDAPQPTEEELEAAWQAYLEAEANKPPELSEVEQLRVENTALQDRLQDVEVIIAELLSI
>NZ_CP009279|6056248:6072755|6063528_6063960_-|WP_042192117.1|DBSCAN-SWA
MIPAIGKSGPITALLEGEVNLERGESPSLTYRMDWDRKRITGQVDGLEAVQQAAAKILRTDRFEHLIYSSDYGTEWQLVLGKDRLLVRAEIRRVINEALLQDERILSLENIEVSFTGENLTFDCKVVTRYGNFQLRKEWNEDV
>NZ_CP009279|6056248:6072755|6064258_6065221_-|WP_042192119.1|DBSCAN-SWA
MELLVKNKEGNLWDISGIVSDISWKTARSGKPATLELTLVDSGIYQHPKFSINNGDIIQFSKDNVDVFYGFVFSIDTGSDQEIKLTAYDQIRYLLGNGSYVLQDVTASDVITKITKDYGLKTGVLENTEYRIPSLIQDDKKLLDIIMGAIGSELQYKGRLMAFYDDFGKLTLRKPESMLLNLVLGAGQYLYDYSLKKSIDDDTYNTIFLYKDNEKSGKRDFFPVSDKDNVKRWGILHLYQKADDKANAAQIQEKANNLLKMHNREKLSLSVQAIGDMRVRAGNFIYVLLDEFKTQVFLVDQCSHKISGGEHTMSLDIKVV
>NZ_CP009279|6056248:6072755|6060076_6060688_-|WP_042192108.1|DBSCAN-SWA
MSYGSSLYSELQYSADKDSSHPGEVEAPDLMQYLPDYYKNVREMEKLQETIGLEIGGLKVGTIDVLDQAFVETATVSLGRWEAELGLNIDSSKSYATRREMIKAKLRGNGTTTPEMIQRTASAFSGGVVEVKEVPDEYRFEIHFVSTLGIPPNMAGLIQIIEEIKPAHLAYEFVFSYTWWDSVKVLNWENAHSKTWNELRTYR
>NZ_CP009279|6056248:6072755|6070705_6071119_-|WP_042192133.1|DBSCAN-SWA
MSVQQLREHITSALERYFPDVPVYVEGEKPQTAYFYPGLISATLDRQREGRYLAVYRFGIRYEKGSLLEAERMADKLSEAMAGMEQEGGSFRVARQAWEAGVEGHGPLFTTDYMVYLQSEKPDPIKMGHMIGGERLK
>NZ_CP009279|6056248:6072755|6070529_6070709_-|WP_042192130.1|DBSCAN-SWA
MSTKVSNGDRFGKEQIVNSSLFTAKEKDVLNVILQDDKSYTIEEAKQSMGLFMNKEVLN
>NZ_CP009279|6056248:6072755|6063956_6064253_-|WP_042132514.1|DBSCAN-SWA
MLDIIKKASLGAVGNTNPVAFSYGTVTEVAPLQIQVDQRFILSGNALVLPESVMECKVELEGREVVVRRGLASGDRVLMVRMQGGQSYIVLDRLVSPI
>NZ_CP009279|6056248:6072755|6068199_6068622_-|WP_042131197.1|portal|DBSCAN-SWA
MSELSLFFAQNVACDTTEEFVVSQRFKDKEGNAVAWKLRSMNEDENQECRKAATRKVKGKNGVYTSEIEPNDYMAKLMTSSVVHPDLKNAELQRSYGVLGAETLLRKMLLPGEFAALGERVQALNGFGTDMNELVDEVKN
>NZ_CP009279|6056248:6072755|6072326_6072755_+|WP_042192135.1|DBSCAN-SWA
MKQDFGDYMKQLRETKGLTINQLAAAAGISGSQISRIENGLRGVPKPTTLRKIAEATGVPYEELMDQAGYLQEQALPSEEIVPEWATSKDKRDFRKMLEDDGELMFDGIPLDKDDKQRIKDVLTGLFWEAKQMNKRKKSNNT
>NZ_CP009279|6056248:6072755|6071544_6072042_-|WP_143759592.1|DBSCAN-SWA
MMNLSALPELDRRRTQVAIESMLEKYRIFKTVTFEAKEASTTYSYTERFHGPTNTVTDQTAAIASYNVDIPAARRAFCSAIDSVVERLDTREQQLVRERYMKRDETYDYTIYNHVFDPPVSKDTYVKIRSKAFYKMALALTDLGLLSLNTLITAPRVKKEKISIT
>NZ_CP009279|6056248:6072755|6065984_6068009_-|WP_042192123.1|DBSCAN-SWA
MAGMQNNIAGIQQVSNQWINDITNQITTQVSANISNSFSATLNRISMKIVNKPVYNITNNYSAAYTRIQASIGGAVQAQERLNDAAEQGATGAEQQAGTWEKITGAFGKAKGVLEKVKGVMEKVLAPAAEQQKWEDLFKAKTGNADVGVAMFDKFKKRALDTGQDVNKSMESVLSFYPKTQNTDQLDKLMDYSTRLSMMSPEGKDIGDTSSAITSAFEGDSSDLASMLQVDKEDLGGLDLVAGTGNMEAFLSTLGDIMTTSGMTSDSLQTMMDSPVNQWQALLGNYNNSLAGMGEGALAALSPLLGILNQAFSDGSFQPIIDGIAIGLAILAQVFSQVVQGALYLWSVLSNPVVLPIVLGVVAGVIALAIAMNASTIATRISSIATGIATAAQGIFNAVMSANPIALVIGLIVALIVAFLGIVAALQPVRDFLANMFRGLGQLVAEFVGFVIDLWTGFVNGIIGAVNFLLDSINKVVGAVGKFIGIESEINLHIEEVDSSQFKKDLQMDIGASFNSGAEKIQNFDINKFKEKLNVGGNKSNNTTLNQWNTTHSGDLSKPLQTPTVPEIPVVPTMNTPSATGSFQNAGTPGNLNTVNRVKQLDSINDTVDISSDDLKMLRELAEIQAIQNFVELTPTVQVTTGNINNAGDIDTIINKIGQKLNEEFVSTAQGVYT
>NZ_CP009279|6056248:6072755|6060691_6061027_-|WP_076300996.1|DBSCAN-SWA
MALKTLIQIRRGLESAIGALAIGELGYCTDSGKLYIGSAAGNVLLVAAQSTGDMLKSIYDTNNNGKVDFAQQADSVAWAGVAGKPAVFPPAAHTHDYLPKGPLTWNQLKGV

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_052404439.1|6056248_6056941_-	hypothetical protein	A0A127AWA8	Bacillus_phage	8.2e-44	55.3
WP_042192098.1|6056912_6057302_-	hypothetical protein	NA	NA	NA	NA
WP_036681274.1|6057294_6057495_-	hypothetical protein	NA	NA	NA	NA
WP_042192100.1|6057538_6057781_-	hypothetical protein	NA	NA	NA	NA
WP_042192102.1|6057872_6058091_-	hypothetical protein	NA	NA	NA	NA
WP_042192104.1|6058114_6058555_-	hypothetical protein	NA	NA	NA	NA
WP_042192106.1|6058568_6060065_-	hypothetical protein	S6B1J7	Thermus_phage	9.9e-10	36.0
WP_042192108.1|6060076_6060688_-	YmfQ family protein	S6BFJ0	Thermus_phage	1.5e-52	54.4
WP_076300996.1|6060691_6061027_-	hypothetical protein	A0A0A7S181	Clostridium_phage	9.6e-06	65.7
WP_042192110.1|6061038_6062061_-	DUF2793 domain-containing protein	A0A0S0MV96	Pseudomonas_phage	1.7e-13	37.9
WP_042192112.1|6062062_6062476_-	hypothetical protein	A0A0A7S1G0	Clostridium_phage	1.1e-30	51.2
WP_042192114.1|6062477_6063536_-|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	1.8e-98	54.5
WP_042192117.1|6063528_6063960_-	DUF2634 domain-containing protein	S6B9X2	Thermus_phage	1.6e-21	48.2
WP_042132514.1|6063956_6064253_-	DUF2577 domain-containing protein	A0A0A7RTJ2	Clostridium_phage	3.1e-16	40.4
WP_042192119.1|6064258_6065221_-	hypothetical protein	A0A0K2CNH3	Brevibacillus_phage	2.0e-88	48.4
WP_042192121.1|6065230_6065983_-	LysM peptidoglycan-binding domain-containing protein	A0A0K2CNM3	Brevibacillus_phage	1.1e-44	40.6
WP_042192123.1|6065984_6068009_-	hypothetical protein	A0A0K2CP22	Brevibacillus_phage	3.2e-19	30.6
WP_076120992.1|6068020_6068200_-	hypothetical protein	NA	NA	NA	NA
WP_042131197.1|6068199_6068622_-|portal	phage portal protein	A0A0A8WJT4	Clostridium_phage	9.8e-24	42.5
WP_042192125.1|6068735_6069206_-|tail	phage tail tube protein	A0A0K2CNG3	Brevibacillus_phage	4.4e-49	61.6
WP_042192128.1|6069207_6070530_-	phage-like element PBSX protein XkdK	A0A0A7RTT5	Clostridium_phage	6.9e-108	47.6
WP_042192130.1|6070529_6070709_-	hypothetical protein	NA	NA	NA	NA
WP_042192133.1|6070705_6071119_-	hypothetical protein	NA	NA	NA	NA
WP_143759592.1|6071544_6072042_-	transcriptional regulator	A0A0C5AJ96	Bacteriophage	2.1e-41	64.9
WP_042192135.1|6072326_6072755_+	transcriptional regulator	S6C481	Thermus_phage	3.5e-21	41.8

Sequences of DBSCAN-SWA_9

Nucleotide sequences of DBSCAN-SWA_9

>NZ_CP009279|6166056:6174762|DBSCAN-SWA
CTTATTCTTTTAGCTCTAAGAGGAAATCTCTCAGGCCCTCACGCCAAGGTCGAATATCCTCAAATCCATTCGTACGTATCGACAGATGCTCCATCACCGAATTCCGAGGACGTGGTGCAGGTCTCGGGAACTGTTCTGTAGCACACGGTTCAAGCTTAGCGGTAAATTTCAAACCTAAAACTTCCTCAGCCTCTGCAAAAATTGCCTGTGTAAATTCAAACCAAGTACATGAGTCGCTATTTGACGCATGGTATACACCATACTTCTCAGTTTGGATAAGCTCAAGTAAGAAACGAGCTAAATCAACTGTATAGGTAGGCGAACCCTTTTGGTCATCGACTACTTGAAGCATTGGCTTTTCTTGACCAAGCTTTAGCATTGTTTTGACAAAGTTATTCCCGTATTTACCATACACCCATGATGTGCGTACGATGAAATACTTAGAGGAGAGGGATTGAACGAGCACCTCGCCCGCACGTTTCGATTTACCATATATACTCTTAGGGTCTGTATTATCATACTCATGGTAAGGCTGTACTCCCAAACCATCAAATACATAATCCGTACTAATGTACACCAGCTTAGCTCCAGCTTTTTCAGAAGCTAGCGCTACGTTTCGACTGCCCGTTGCATTAATTAAATAAGCTGCATCGATGTCACTTTCTGCCGCATCTACTGCTGTATGCGCAGCACAATGAATGACAGCATCCGGTCCAAACTCACCAATAACCTGGATACACTGATCCAGATCGGTGATATCCATCTCTTGACGGTCACAGCCCATCACTTGGTGACCTTGATGCTGGATTAGTAAAACTACGTCCTGGCCTAGTTGTCCGGCCGCGCCTGTAACAAGTACCTTCAGTTGAGCCATTATAGAGATTCTCCCAAACGATCGCCATATTGTAATTCAGCGTACTTCTGGTATTCCCCAGATTGAATGCGAGTCCACCATTCTCGGTTATTGAGATACCATTGGATGGTTTCTTTAATACCTGTTTCAAACGTATGCTTCGGCTTCCAACCCAGTTCGTTCATAATCTTGGTAGGATCAATTCCATAGCGTCGATCATGACCCGGACGGTCTTGAACATAAGTAATCAGTGAATCAGGTTTGCCAAGTTCCTGCAATACTGTGTTCACGATATGCACATTTGTACGTTCGTTATTGCCACCAATGTTGTATACTTCACCGTTCACGCCCTTGTGGATAACCAAATCAATCGCGCTGCAGTGATCCTCAACATACAACCAGTCACGGATATTCATCCCATCGCCATATACAGGCAACGCTTGATCCGCAAGTGCGCGGGAGATCATAAGCGGAATAAGCTTCTCAGGGAATTGGTACGGGCCATAATTGTTCGAGCAGCGGGTAATGTTCACTGGCAGTCCGAATGTCTCATGGTATGCACGTACAAGCAAGTCGCCACCAGCTTTACTTGCCGAATATGGACTGTTCGGAGTCAAAGGAGTTTCTTCAGTAAACAAACCGGTTGCTCCAAGTGATCCGTATACCTCATCCGTAGAAACCTGAACGAATTTAGTAACACTGTATTTTTTCGCCGCATCCAAAAGTACTTGTGTTCCAAGCACGTTCGTCTTCACAAACACTTCTGGCTCCAAAATACTCCGATCCACATGCGATTCAGCCGCGAAATTTACCACTACATCAACACCTTGGCTAAACAAAGCATCCATTGCCTGTACATCTGTAATGTCTGCTTTTACGAACTTGTGGTTCGGATGATTTTCAATTGACTTCAAATTCTCCAAATTACCTGCATACGTCAACGCGTCTACGTTAACGATTTGATAATCAGGATGTTGTTGCAGCATGTATAATACAAAGTTGCTGCCGATAAAGCCGGCTCCGCCGGTAACTAGCAGTTTCATGTGTAGCCCACCTTTATTTCATGAAATATTGTGTTTATAACTCAAAATTAAGTTCAGCGTCCTTCAGCAATGGATGACGCTGATCCTTATCCGATAATACTGGACTAGAAGTCGGCCAATCAATACCTAAGGCTGGATCATTCCATAATATGCCGCGATCATTTTCGGGGGAATAATATTCGTCCACCTTATATAACACTTGGGTGTTCGGAACCAATGTGCAGAATCCATGCGCGAAGCCCTTAGGTACAAGCAGTTGGCGTTTGTTATATTCGCTAAGTATTACTCCGACCCATTGACCAAATGTAGGAGAATTACGACGGATATCTACGATAACATCGTAAATAGCTCCAGTTAGAACACGGATCAATTTCGTTTGAGCTTTTGGGTTCAGCTGGTAGTGAAGACCACGCAGCACTCCAACGTCTGCAGAGAGGGACTGATTGTCTTGAATGAAATTGTAGTTTACGCCGAGCTTATGCATTACTTCTTCGTTGTAGCTTTCCATGAAAAATCCACGGTTGTCGCCGTGGACTACAGGTTCTAAAATGCTCGCACCTTGTAGTTGTAAGGGTGTAACTTTCATATTGCAAACCTCCTTCTCATCTAAAGTTTCAGTTTTCCGAATTCTTCACCAAATAGAAGGTCTTGAGCCAAGTTATGTGCTTTAGCTAATGAGGCATGTGTACCTGCATCTGTCCACCAACCTTGTAGAACATCAAAGGTCAATTCTCCACGTTTAATATATGCATTATTAACATCAGTAATTTCTAATTCTCCACGTGCAGAAGGTGTAATCGTTTTGATAATATTAAACACTTCACTATCAAACATATATATCCCTGTGACTGCATAGCCAGACTTGGGTTCACTAGGCTTCTCTTCGATAGACAATATCCGATTCCCCTCTAATTCGGGCACACCAAAACGCTTAGGATCAGGAACTTCCTGAATCAGGATCTTAGCACCTGTCTTTTGCTCACGGAAATTACGTGCATAAGGAGCGATATCATCAGCAAACACGTTATCACCAAGGATAACGATCATTTGATCATCCCCGACAAATTGCTCTGCCAAGTCCAAAGCCTGCGCAATTCCGCCTGCCTCATCTTGTACTTTGTAAGTAAAGCAAACACCCATTTCATGTCCGCTACCTAATAGATTAACTACATCACCCATATGTTCTTTACCAGTAACGATCAGAATATCTGTTACATCAGCTTGCTTCAACTTATAAACGGAATGAAAAATCATTGGGTATTTGCCTACGGGAAGAAGATGTTTATTTGTTACCTTTGTTAATGGGTATAAGCGCGAGCCTGTACCTCCTGCTAAAATAATACCTTTCATTGTATTGCCTCCATTCATTTACTTTTAATAATAAGTTTAGAAAGTGTGTAGGTGATCGGAATTGTCACTACAATAACTATTAAGGGTACGATTTGTTTCGATAGATTTAAATGCTCAACTAAAACATATAACATAAACAAATTAATTAAATACTGTACCAGATATACGATCGGAAACTTAAGAAACTTTCTAAATAAAACCTTTTCTTTAAATACAAAAGCTGTATTCAAGTAATAGGAAAGAAATATTCCAGAAATATAAGAAATTGTATAAGACATAGAATAACTAAGGAATTCAAGAAGGAGTAAATAGACCAGATATGTTGCTAATGTATTTATTCCTCCGCTAATGACAAATTTCAAAAATTGTTTACTCAAAAGTTTGGTCAACAACGTAGGATGGTCTTTCTCTACTTTCATCTAATATCCTCCAAAGATATTCACCTATAATTCCTAACATAATCATTATAATCCCTAATAAAAAAGTAATTAGAGCTATAATTGTAGTCCATCCTTGTAACTCAATGATACCAAAGACAGTACTAATTATAACAAAAACACCATATAGAAAACTCAGAAAAGCTGTAACAAACCCGATGAATGACATGAAACGAATAGGTGTGTATGAGAAACTTACAAATGAATCAATAAAAAGTTTTACTTTCTTAGCGAGTGTCCACCTAGATTTACCCAGTTTTCTTTCTTGCCTCACATAAGGAATTTGTACTTGATCATGTCCAAGCCAATATATGAGACTCATAACACTCGTATTCTTCTCTTGAATTTCCAAAACTTCTTGTACAACCTGTCTATCAATTAACAAAAAATCAAATCCACCTTTTGGATATCCCTTTAATGCGAATTTTTCCAATAAAAAATAATAGGTATTTGAAAACATCTTCTGAGAGAATGACTCTTCTCTATCTGCTCTTGTTCCAAGTACAACTTTTATGCCTGTTCTCCAATGTTCTACCATCTCTTTAAACATTTCAGGAGGATCTTGTAAATCAGCAGCTATAATGCCGACACAATCGCCAGTAGTATATCTTAAGCCCGCCTGTATAGCCGACATCGAACCAAAATTACGACTTAGCTTAATAACTTTAATCCGAGAATCTTGTTCTTTAGCTTCCATCAATAAAGAAAATGAGTTGTCTTTTGAACCATCATCGACAAAAACAAATTCAAAATCACAATTGGGTATAATAGTCTCTAAATTCTGCAATCGTGGGATAGTATGTGGAATGTTTAACTCATTAAAGTATATAGGGACGACAATAGATAACTTAATACGTTCTGAAATCATTCACAACCTCCACAACTTTCTTCACATCTTCTAAATCCATTACCGGACTTATTGGGAGGCTAACAATTTCCGAATGGATTTTTTCAGAGATAGGGAAGGATAGTTCATTCCATTCTTTATATGCTTCCTGTTTATGAGGCGGAATAGGGTAGTGAATCATAGTTTGAATACCCTTTTGGGTCATATAGTTAATAAAATCAGTTCTAAAGGACGTTCTAACTACAAATACATGCCAAACATGTGATTCCGATTTCTCCTCAACAAATGGCAATACAAGATTTTCATTATTGATATTATTCAAGTAATATGATGCGATAGTTCTTCTATGACTGTTATCTTGATCTAGAAATTTTAATTTTTCACTCAAAATTGGTGCTTGAAATTCATCCAATCTGCTATTATAACCTTTAAAAATATTTTCATATTTTTTATGTGATCCATAATTTCTTAAAGCATGAAGATTTGTATATAGTTTCTCATCATTAGTAGTGATGGCACCTGCATCGCCTAAGGCCCCAAGATTTTTACCAGGATAAAAACTGAATGCTGCAGCATCCCCTAAGTTTCCTACCTTTCTATCAGCATAAACAGCACCGTGAGCCTGCGCACAATCTTCGATTATCTTCAGGTTGTATTTTTCTGCAATAATCTTAATTGGCGTCATATTACATGCTTGACCATAAAGGTGAACAACTAGAATCGCCTTTGTATTAGGAGTAATACTTTCTTCAATTTTTTCAGGGTCTAGGTTATATGTTAGTAAGTTAGGTTCGACTAGCACAGGTATTGCGCCATTAGCGGATATGGATAATATAGACGCAATATAGGTATTCGAAGGCACAATAATTTCGTCTCCAGGACCGATATCATAAGCTCTAATTATTAATTCCAAAGCATCTAATCCATTAGCTACTCCGAGAGCATATTTGGTGCCACAATAATCAGTAAATTCCGATTCAAAAGATTTAACCTCTTCACCCATTATATACCATCCAGAGTGTAGAACTTTACGAACACTATTTAAAATAGCTTCTTCATGACGTAGATTGATTTTCTTCAGATCGAGGAAAGGGATCATGTTTGTTCACCTATTTCATTAATTTAATGTTGCTCTACTATAACTTTATCTTCCAGTAAGTATTGTTTACTACAAGCAGAACATAACAATTCATTATTGAGTTTTTCTCCACAATTACATATATATCCTTGGAATTTTGCTGGATTACCATACCATAACGTATTGTTTGGAATGTTTTTAGTCACTAAAGACCCTGCTCCAATCATAGCGTACTTACCAATTGTATTCCCTGCTATAATTGTTGCATTTGCACCTATTGAAACCCATTCTTCAAGCACAGTCTTCAAAAATTCAGTTGGGTACTGTTTGGAACGAGGTCTCAAATCATTAGTAAAAGTAACATTCGGACCAATAAAAACATTATCTTCTATTCTAACACCATCCCAAATATACACTCCTGATTTAACAGTAACATTATCCCCCAAGATTACATCATTTTCGATGAAGGTATGATCGTTAATATTACAGTTCGAGCCAATCACAGCATTCGGTAAAATATGTGCAAACGCCCAAATTCGAGTGTCCACTCCAATTTTCTCTGATTCGACAATAGCCTGTGGATGTGCAAAGTGATGTTTCATCCCCCATACACCTCTATAAATTTGTCATAATCACGAATATAATCTGCTGAATCATATAAGTGGGAAGCGAGAACGAGTAATACGCAATCTGAAGAAAAATCATACATTTCATGCCAATCATTTGGTTCAAGAATGAGAACTTTGGTAGGAGAATCTAATAATATATCCGTTTTTCTTTTCGTATTATCCAAATAAACTTTACAGCTTCCTGATACGCTTATTAATGCTTGTCTAGTTTTATAATGAGCGTGATATCCACGGCGTATATTGGATAAAGTTCCATAAATATAAAACACCCTCTTAATGTCAAACGGAATAGTGTTCTCTGCCTCAATGACAGTTAAATGCCCTCTTTCATCACCAAGCATGGTACTTTCAATGATAGAGCTTTCTAGGGCTTCACTTTCCATACTTATCATACCCTCTCATATTTCAATTCTTGTAATTATCAATTAATTCATGTTGTTACTACTAATCATTTAAAAAAACTAATTTTTCTCACTTCAAAAGTTGACTGTGCGGGCGGATCTATCCGAAGCGATATAAGATTATTCATCAGTTGATTCCTATCACAATAAATCTTATTTATGCCCTTCTTCACTTTAATAGTCCCACTAAACTTTTCGCTGTAACTCTCATTCTCTTGAAGTAAGAATAATTGCATATCCCCATCGACACTAGAATTTATCTCAAATGAAATAAATTTATATGAATCCTCCTCAAGCTTATGACCAAGCGATATTGAAACATAGGGATCTAATTTACCTGCCTTTATAATAAGTCCACTACTATCAGCCTTCTCTATTTCTAGATCATTAAAATATTCTACTTTTTCAGTAATATTCAAATCTGAAATCATTTCATTTTGGATTGTTGAGTCATCAAAATCATAATGTAAATTCAGCTTATACTTTTCAGGGTTTTCTGAGAGATTGACAATAATAAGATCATTTATTAACGCCACGGAACCTTTATGCGGCCAGACAGGCATAGAATCCGCTATTTTTAATGCCTTTTCTCTTTGTTCTTCCGTCGGATCCAAATAATCATATCCTAAAGATTTCATGAAATTACCAATCCTAACACTATTGCCTCCATCCCATTCAAAAAAAGAAAACCCTAATACCTCTTGTTTAATAACATTTGCCCTTTTCGCTTGCACATGCTTACCCAGATAAACAACTGGGTATGGCGGTGTTTCTCCCAAGTCAAGATCCATTATTCTATATCCAATTTGATTGGCTATTTTCACATCTTCTTGATATCTATTATAATCGCTATAAAACAGTTGAGCCATTGACTGAGATTGATAGAAAACGGTAATTATTGCAAAGGTTATAAATGCAATTTTGTAAATTTTTTTATTCATTATTATATAAAGTAAGTACCAACTTGCAGATATAAATAACACTATAGCAAAATTCGCCCTAATCGGCATTGGAGATCCTAGCAAAATAGACATCAAAAAGGGAGAAATGATAAAACCAAGGAATAATACGACTATTATCCAATCGGTTCTTCTTACTTCTGCACGTATCAAAGCTTTATAGAAGAAAAATAATAAAAGCAAGATACTAACAATTATACTTGGTAATATAACATTACTACCGTGTATGACATCTCCCATAACAATTCCTTTAATGTTGCCGAGCAAGTTTCTGACTATAGTACTTGGAGCCTCTTTACCCCAAAGAAAAAAACCTTCAACATAATCTGACTTAGGAATAAATAGTGAAATTACTGTTTCGATAATCTTATAAATTATAAGACTAACCACTGTAACAGTTATATATTTCAAGATTATTATCAGGTAATCTTTGAAAACAACATTGATATTTTCTTTATGTAAAGATACCAAATTTATCAATGTAATTAAAATTACCCCACATATAAAAGCTGGTAAAAATGCTTGGTATATCGAAATCGCTAAAACTAATAATAGTAGACCTATCATCATATAATATTTATCTTTTCTAAAAAGCGCCCATTTAGCAATAAGTAACGTAGCTATTGAAATAAATATCCATCCAATTCCCAGTTCAATACTCATTATAGAAAACCCTATATTTTCTGAATGGGCTGGAAAGCTTAAAAATAATAAAGCTACAGTTAATCCACCAAAATCAAACTTTCTTTCATTTTTACTAGTATTCAAACAACTACTAATAGCATAAGCCCATATCAGACTAGTAAAGCTGAGTGCCGATACAGATAAAAAGGTACTTGTAATAGAATTAGTCTGCCCACTAAAAAATAAAGTCTTTAGTATTGATATCCCAAAACGACCCTGCATACTCCAAATAGTTATAGCATCTCCAACTCGAAATAAAGCATTCTCTTCATCTATAGAAAGTGTAAAATGTGTTAATGGAAATCCGTAGGCGAATAGAGCTACAAAAAATATAAAAACACAAAATAACTTATTACTTTTCATATAAGAAAAAAATGTTTGAAATTCTTCACTAATTTCTAATGAACTTCTCTTGAAAAACCTCAT

Protein sequences of DBSCAN-SWA_9

>NZ_CP009279|6166056:6174762|6170586_6171684_-|WP_042192252.1|DBSCAN-SWA
MIPFLDLKKINLRHEEAILNSVRKVLHSGWYIMGEEVKSFESEFTDYCGTKYALGVANGLDALELIIRAYDIGPGDEIIVPSNTYIASILSISANGAIPVLVEPNLLTYNLDPEKIEESITPNTKAILVVHLYGQACNMTPIKIIAEKYNLKIIEDCAQAHGAVYADRKVGNLGDAAAFSFYPGKNLGALGDAGAITTNDEKLYTNLHALRNYGSHKKYENIFKGYNSRLDEFQAPILSEKLKFLDQDNSHRRTIASYYLNNINNENLVLPFVEEKSESHVWHVFVVRTSFRTDFINYMTQKGIQTMIHYPIPPHKQEAYKEWNELSFPISEKIHSEIVSLPISPVMDLEDVKKVVEVVNDFRTY
>NZ_CP009279|6166056:6174762|6172740_6174762_-|WP_042192258.1|DBSCAN-SWA
MRFFKRSSLEISEEFQTFFSYMKSNKLFCVFIFFVALFAYGFPLTHFTLSIDEENALFRVGDAITIWSMQGRFGISILKTLFFSGQTNSITSTFLSVSALSFTSLIWAYAISSCLNTSKNERKFDFGGLTVALLFLSFPAHSENIGFSIMSIELGIGWIFISIATLLIAKWALFRKDKYYMMIGLLLLVLAISIYQAFLPAFICGVILITLINLVSLHKENINVVFKDYLIIILKYITVTVVSLIIYKIIETVISLFIPKSDYVEGFFLWGKEAPSTIVRNLLGNIKGIVMGDVIHGSNVILPSIIVSILLLLFFFYKALIRAEVRRTDWIIVVLFLGFIISPFLMSILLGSPMPIRANFAIVLFISASWYLLYIIMNKKIYKIAFITFAIITVFYQSQSMAQLFYSDYNRYQEDVKIANQIGYRIMDLDLGETPPYPVVYLGKHVQAKRANVIKQEVLGFSFFEWDGGNSVRIGNFMKSLGYDYLDPTEEQREKALKIADSMPVWPHKGSVALINDLIIVNLSENPEKYKLNLHYDFDDSTIQNEMISDLNITEKVEYFNDLEIEKADSSGLIIKAGKLDPYVSISLGHKLEEDSYKFISFEINSSVDGDMQLFLLQENESYSEKFSGTIKVKKGINKIYCDRNQLMNNLISLRIDPPAQSTFEVRKISFFK
>NZ_CP009279|6166056:6174762|6171707_6172265_-|WP_042192254.1|DBSCAN-SWA
MKHHFAHPQAIVESEKIGVDTRIWAFAHILPNAVIGSNCNINDHTFIENDVILGDNVTVKSGVYIWDGVRIEDNVFIGPNVTFTNDLRPRSKQYPTEFLKTVLEEWVSIGANATIIAGNTIGKYAMIGAGSLVTKNIPNNTLWYGNPAKFQGYICNCGEKLNNELLCSACSKQYLLEDKVIVEQH
>NZ_CP009279|6166056:6174762|6169670_6170606_-|WP_042192250.1|DBSCAN-SWA
MISERIKLSIVVPIYFNELNIPHTIPRLQNLETIIPNCDFEFVFVDDGSKDNSFSLLMEAKEQDSRIKVIKLSRNFGSMSAIQAGLRYTTGDCVGIIAADLQDPPEMFKEMVEHWRTGIKVVLGTRADREESFSQKMFSNTYYFLLEKFALKGYPKGGFDFLLIDRQVVQEVLEIQEKNTSVMSLIYWLGHDQVQIPYVRQERKLGKSRWTLAKKVKLFIDSFVSFSYTPIRFMSFIGFVTAFLSFLYGVFVIISTVFGIIELQGWTTIIALITFLLGIIMIMLGIIGEYLWRILDESRERPSYVVDQTFE
>NZ_CP009279|6166056:6174762|6168557_6169301_-|WP_042192244.1|DBSCAN-SWA
MKGIILAGGTGSRLYPLTKVTNKHLLPVGKYPMIFHSVYKLKQADVTDILIVTGKEHMGDVVNLLGSGHEMGVCFTYKVQDEAGGIAQALDLAEQFVGDDQMIVILGDNVFADDIAPYARNFREQKTGAKILIQEVPDPKRFGVPELEGNRILSIEEKPSEPKSGYAVTGIYMFDSEVFNIIKTITPSARGELEITDVNNAYIKRGELTFDVLQGWWTDAGTHASLAKAHNLAQDLLFGEEFGKLKL
>NZ_CP009279|6166056:6174762|6169315_6169720_-|WP_042192248.1|DBSCAN-SWA
MKVEKDHPTLLTKLLSKQFLKFVISGGINTLATYLVYLLLLEFLSYSMSYTISYISGIFLSYYLNTAFVFKEKVLFRKFLKFPIVYLVQYLINLFMLYVLVEHLNLSKQIVPLIVIVVTIPITYTLSKLIIKSK
>NZ_CP009279|6166056:6174762|6166056_6166920_-|WP_042194606.1|DBSCAN-SWA
MKVLVTGAAGQLGQDVVLLIQHQGHQVMGCDRQEMDITDLDQCIQVIGEFGPDAVIHCAAHTAVDAAESDIDAAYLINATGSRNVALASEKAGAKLVYISTDYVFDGLGVQPYHEYDNTDPKSIYGKSKRAGEVLVQSLSSKYFIVRTSWVYGKYGNNFVKTMLKLGQEKPMLQVVDDQKGSPTYTVDLARFLLELIQTEKYGVYHASNSDSCTWFEFTQAIFAEAEEVLGLKFTAKLEPCATEQFPRPAPRPRNSVMEHLSIRTNGFEDIRPWREGLRDFLLELKE
>NZ_CP009279|6166056:6174762|6172261_6172675_-|WP_042192256.1|DBSCAN-SWA
MESEALESSIIESTMLGDERGHLTVIEAENTIPFDIKRVFYIYGTLSNIRRGYHAHYKTRQALISVSGSCKVYLDNTKRKTDILLDSPTKVLILEPNDWHEMYDFSSDCVLLVLASHLYDSADYIRDYDKFIEVYGG
>NZ_CP009279|6166056:6174762|6167985_6168537_-|WP_042192241.1|DBSCAN-SWA
MKVTPLQLQGASILEPVVHGDNRGFFMESYNEEVMHKLGVNYNFIQDNQSLSADVGVLRGLHYQLNPKAQTKLIRVLTGAIYDVIVDIRRNSPTFGQWVGVILSEYNKRQLLVPKGFAHGFCTLVPNTQVLYKVDEYYSPENDRGILWNDPALGIDWPTSSPVLSDKDQRHPLLKDAELNFEL
>NZ_CP009279|6166056:6174762|6166928_6167951_-|WP_042192239.1|DBSCAN-SWA
MKLLVTGGAGFIGSNFVLYMLQQHPDYQIVNVDALTYAGNLENLKSIENHPNHKFVKADITDVQAMDALFSQGVDVVVNFAAESHVDRSILEPEVFVKTNVLGTQVLLDAAKKYSVTKFVQVSTDEVYGSLGATGLFTEETPLTPNSPYSASKAGGDLLVRAYHETFGLPVNITRCSNNYGPYQFPEKLIPLMISRALADQALPVYGDGMNIRDWLYVEDHCSAIDLVIHKGVNGEVYNIGGNNERTNVHIVNTVLQELGKPDSLITYVQDRPGHDRRYGIDPTKIMNELGWKPKHTFETGIKETIQWYLNNREWWTRIQSGEYQKYAELQYGDRLGESL

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042194606.1|6166056_6166920_-	dTDP-4-dehydrorhamnose reductase	I7HXC9	Enterobacteria_phage	1.1e-32	34.7
WP_042192239.1|6166928_6167951_-	dTDP-glucose 4,6-dehydratase	A0A1D7XFE8	Escherichia_phage	3.1e-79	47.9
WP_042192241.1|6167985_6168537_-	dTDP-4-dehydrorhamnose 3,5-epimerase	A0A291LA62	Escherichia_phage	1.7e-39	46.1
WP_042192244.1|6168557_6169301_-	NTP transferase domain-containing protein	I7I009	Enterobacteria_phage	2.2e-50	45.3
WP_042192248.1|6169315_6169720_-	GtrA family protein	NA	NA	NA	NA
WP_042192250.1|6169670_6170606_-	glycosyltransferase family 2 protein	I1TED8	Salmonella_phage	1.0e-36	30.1
WP_042192252.1|6170586_6171684_-	DegT/DnrJ/EryC1/StrS family aminotransferase	NA	NA	NA	NA
WP_042192254.1|6171707_6172265_-	N-acetyltransferase	NA	NA	NA	NA
WP_042192256.1|6172261_6172675_-	WxcM-like domain-containing protein	NA	NA	NA	NA
WP_042192258.1|6172740_6174762_-	hypothetical protein	O21944	Shigella_phage	3.2e-11	23.8