CRISPRimmunity

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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_CP023993	Streptomyces malaysiensis strain DSM 4137 plasmid unnamed, complete sequence	0 crisprs	DEDDh	0	0	0	0
NZ_CP023992	Streptomyces malaysiensis strain DSM 4137 chromosome, complete genome	18 crisprs	csa3,WYL,casR,cas4,DEDDh,RT,c2c9_V-U4,PD-DExK,cas3,DinG	2	7	4	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP023992_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_1

2001702-2001787

Orphan

Consensus_repeat	Method
CGGTCCGCGCGCGCCCGGGGGCGTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_1

>merge|NZ_CP023992|1|2001702-2001787|CRISPRCasFinder
CGGTCCGCGCGCGCCCGGGGGCGTTGCCCATCACCTCGGAAGGAAACCCATGGCCACCCGCCGGTTCGCGCGCGCCCGGGGGCGGT

>NZ_CP023992|1|1|2001702-2001787|CRISPRCasFinder
CGGTCCGCGCGCGCCCGGGGGCGTT	GCCCATCACCTCGGAAGGAAACCCATGGCCACCCGC
CGGTTCGCGCGCGCCCGGGGGCGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_161370249.1\|1999900_2000605_-\|MSMEG_4193-family-putative-phosphomutase	unknown	unknown	gnl\|CDD\|163560
NZ_CP023992.1\|WP_069869005.1\|2004298_2005279_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381313
NZ_CP023992.1\|WP_099013151.1\|1993129_1993906_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP023992.1\|WP_014059547.1\|2008936_2009125_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069869006.1\|2003121_2004171_-\|LLM-class-F420-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|274647
NZ_CP023992.1\|WP_079257036.1\|2008214_2008889_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099016850.1\|2001817_2002624_-\|ferritin-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|153097
NZ_CP023992.1\|WP_099013155.1\|1998239_1999088_-\|SCO1664-family-protein	unknown	unknown	gnl\|CDD\|274813
NZ_CP023992.1\|WP_099013150.1\|1991971_1993006_-\|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|380478
NZ_CP023992.1\|WP_099013154.1\|1996814_1998044_-\|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase	unknown	unknown	gnl\|CDD\|183518
NZ_CP023992.1\|WP_099013149.1\|1990373_1991969_-\|sugar-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224053
NZ_CP023992.1\|WP_099013156.1\|2009336_2010230_-\|chaplin	unknown	unknown	gnl\|CDD\|367652
NZ_CP023992.1\|WP_099013153.1\|1995548_1996697_+\|PAC2-family-protein	unknown	unknown	gnl\|CDD\|378251
NZ_CP023992.1\|WP_099013158.1\|2014197_2015139_-\|RNA-methyltransferase	unknown	unknown	gnl\|CDD\|334588
NZ_CP023992.1\|WP_069869009.1\|1999186_1999777_-\|DUF3090-domain-containing-protein	unknown	unknown	gnl\|CDD\|213872
NZ_CP023992.1\|WP_099013152.1\|1993902_1995330_-\|fuconate-dehydratase	unknown	unknown	gnl\|CDD\|239440
NZ_CP023992.1\|WP_099016851.1\|2005443_2007894_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273632
NZ_CP023992.1\|WP_069869007.1\|2000694_2001687_+\|magnesium/cobalt-transporter-CorA	unknown	unknown	gnl\|CDD\|213364
NZ_CP023992.1\|WP_099013157.1\|2012176_2013862_-\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|238206
NZ_CP023992.1\|WP_069869001.1\|2010557_2011895_-\|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl\|CDD\|181163

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_161370249.1\|1999900_2000605_-\|MSMEG_4193-family-putative-phosphomutase	gnl\|CDD\|163560	TIGR03848, MSMEG_4193, probable phosphomutase, MSMEG_4193 family. A three-gene system broadly conserved among the Actinobacteria includes MSMEG_4193 and homologs, a subgroup among the larger phosphoglycerate mutase family protein (pfam00300). Another member of the trio is a probable kinase, related to phosphatidylinositol kinases; that context supports the hypothesis that this protein acts as a phosphomutase.	1.13556e-111
NZ_CP023992.1\|WP_069869005.1\|2004298_2005279_+\|aldo/keto-reductase	gnl\|CDD\|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	3.28073e-104
NZ_CP023992.1\|WP_099013151.1\|1993129_1993906_-\|SDR-family-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. 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 prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, 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.	3.8793e-58
NZ_CP023992.1\|WP_069869006.1\|2003121_2004171_-\|LLM-class-F420-dependent-oxidoreductase	gnl\|CDD\|274647	TIGR03559, F420_Rv3520c, probable F420-dependent oxidoreductase, Rv3520c family. Members of this protein family are predicted to be oxidoreductases dependent on coenzyme F420. The family includes a single member in Mycobacterium tuberculosis (Rv3520c/MT3621) but four in Mycobacterium smegmatis. Prediction that this family is F420-dependent is based primarily on Partial Phylogenetic Profiling vs. F420 biosynthesis. [Unknown function, Enzymes of unknown specificity].	1.45431e-136
NZ_CP023992.1\|WP_099016850.1\|2001817_2002624_-\|ferritin-like-domain-containing-protein	gnl\|CDD\|153097	cd00657, Ferritin_like, Ferritin-like superfamily of diiron-containing four-helix-bundle proteins. Ferritin-like, diiron-carboxylate proteins participate in a range of functions including iron regulation, mono-oxygenation, and reactive radical production. These proteins are characterized by the fact that they catalyze dioxygen-dependent oxidation-hydroxylation reactions within diiron centers; one exception is manganese catalase, which catalyzes peroxide-dependent oxidation-reduction within a dimanganese center. Diiron-carboxylate proteins are further characterized by the presence of duplicate metal ligands, glutamates and histidines (ExxH) and two additional glutamates within a four-helix bundle. Outside of these conserved residues there is little obvious homology. Members include bacterioferritin, ferritin, rubrerythrin, aromatic and alkene monooxygenase hydroxylases (AAMH), ribonucleotide reductase R2 (RNRR2), acyl-ACP-desaturases (Acyl_ACP_Desat), manganese (Mn) catalases, demethoxyubiquinone hydroxylases (DMQH), DNA protecting proteins (DPS), and ubiquinol oxidases (AOX), and the aerobic cyclase system, Fe-containing subunit (ACSF).	0.000947112
NZ_CP023992.1\|WP_099013155.1\|1998239_1999088_-\|SCO1664-family-protein	gnl\|CDD\|274813	TIGR03843, Phosphatidylinositol_3-_and_4-kinase, conserved hypothetical protein. This model represents a protein family largely restricted to the Actinobacteria (high-GC Gram-positives), although it is also found in the Chloroflexi. Distant similarity to the phosphatidylinositol 3- and 4-kinase is suggested by the matching of some members to pfam00454.	2.95869e-120
NZ_CP023992.1\|WP_099013150.1\|1991971_1993006_-\|sugar-ABC-transporter-substrate-binding-protein	gnl\|CDD\|380478	cd01536, PBP1_ABC_sugar_binding-like, periplasmic sugar-binding domain of active transport systems that are members of the type 1 periplasmic binding protein (PBP1) superfamily. Periplasmic sugar-binding domain of active transport systems that are members of the type 1 periplasmic binding protein (PBP1) superfamily. The members of this family function as the primary receptors for chemotaxis and transport of many sugar based solutes in bacteria and archaea. The sugar binding domain is also homologous to the ligand-binding domain of eukaryotic receptors such as glutamate receptor (GluR) and DNA-binding transcriptional repressors such as LacI and GalR. Moreover, this periplasmic binding domain, also known as Venus flytrap domain, undergoes transition from an open to a closed conformational state upon the binding of ligands such as lactose, ribose, fructose, xylose, arabinose, galactose/glucose, and other sugars. This family also includes the periplasmic binding domain of autoinducer-2 (AI-2) receptors such as LsrB and LuxP which are highly homologous to periplasmic pentose/hexose sugar-binding proteins.	2.53387e-55
NZ_CP023992.1\|WP_099013154.1\|1996814_1998044_-\|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase	gnl\|CDD\|183518	PRK12418, PRK12418, cysteinyl-tRNA synthetase; Provisional.	0
NZ_CP023992.1\|WP_099013149.1\|1990373_1991969_-\|sugar-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224053	COG1129, MglA, ABC-type sugar transport system, ATPase component [Carbohydrate transport and metabolism].	0
NZ_CP023992.1\|WP_099013156.1\|2009336_2010230_-\|chaplin	gnl\|CDD\|367652	pfam03777, DUF320, Small secreted domain (DUF320). Small domain found in a family of secreted streptomyces proteins. It occurs singly or as a pair. Many of the domains have two cysteines that may form a disulphide bridge.	1.9579e-13
NZ_CP023992.1\|WP_099013153.1\|1995548_1996697_+\|PAC2-family-protein	gnl\|CDD\|378251	pfam09754, PAC2, PAC2 family. This PAC2 (Proteasome assembly chaperone) family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 247 and 307 amino acids in length. These proteins function as a chaperone for the 26S proteasome. The 26S proteasome mediates ubiquitin-dependent proteolysis in eukaryotic cells. A number of studies including very recent ones have revealed that assembly of its 20S catalytic core particle is an ordered process that involves several conserved proteasome assembly chaperones (PACs). Two heterodimeric chaperones, PAC1-PAC2 and PAC3-PAC4, promote the assembly of rings composed of seven alpha subunits.	2.31637e-51
NZ_CP023992.1\|WP_099013158.1\|2014197_2015139_-\|RNA-methyltransferase	gnl\|CDD\|334588	pfam01555, N6_N4_Mtase, DNA methylase. Members of this family are DNA methylases. The family contains both N-4 cytosine-specific DNA methylases and N-6 Adenine-specific DNA methylases.	5.18867e-13
NZ_CP023992.1\|WP_069869009.1\|1999186_1999777_-\|DUF3090-domain-containing-protein	gnl\|CDD\|213872	TIGR03847, TIGR03847, conserved hypothetical protein. The conserved hypothetical protein described here occurs as part of the trio of uncharacterized proteins common in the Actinobacteria.	3.83161e-88
NZ_CP023992.1\|WP_099013152.1\|1993902_1995330_-\|fuconate-dehydratase	gnl\|CDD\|239440	cd03324, rTSbeta_L-fuconate_dehydratase, Human rTS beta is encoded by the rTS gene which, through alternative RNA splicing, also encodes rTS alpha whose mRNA is complementary to thymidylate synthase mRNA. rTS beta expression is associated with the production of small molecules that appear to mediate the down-regulation of thymidylate synthase protein by a novel intercellular signaling mechanism. A member of this family, from Xanthomonas, has been characterized to be a L-fuconate dehydratase. rTS beta belongs to the enolase superfamily of enzymes, characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	0
NZ_CP023992.1\|WP_099016851.1\|2005443_2007894_+\|hypothetical-protein	gnl\|CDD\|273632	TIGR01448, recD_rel, helicase, putative, RecD/TraA family. This model describes a family similar to RecD, the exodeoxyribonuclease V alpha chain of TIGR01447. Members of this family, however, are not found in a context of RecB and RecC and are longer by about 200 amino acids at the amino end. Chlamydia muridarum has both a member of this family and a RecD. [Unknown function, Enzymes of unknown specificity].	2.94672e-30
NZ_CP023992.1\|WP_069869007.1\|2000694_2001687_+\|magnesium/cobalt-transporter-CorA	gnl\|CDD\|213364	cd12830, MtCorA-like, Mycobacterium tuberculosis CorA-like subfamily. This bacterial subfamily belongs to the Thermotoga maritima CorA (TmCorA)-like family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subfamily includes the Mg2+ transporter Mycobacterium tuberculosis CorA (which also transports Co2+). Thermotoga maritima CorA forms funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport by a related protein, Saccharomyces cerevisiae Alr1p. Natural variants in this signature sequence may be associated with the transport of different divalent cations. The functional diversity of the MIT superfamily may also be due to minor structural differences regulating gating, substrate selection, and transport.	1.71747e-165
NZ_CP023992.1\|WP_099013157.1\|2012176_2013862_-\|recombinase-family-protein	gnl\|CDD\|238206	cd00338, Ser_Recombinase, Serine Recombinase family, catalytic domain; a DNA binding domain may be present either N- or C-terminal to the catalytic domain. These enzymes perform site-specific recombination of DNA molecules by a concerted, four-strand cleavage and rejoining mechanism which involves a transient phosphoserine linkage between DNA and serine recombinase. Serine recombinases demonstrate functional versatility and include resolvases, invertases, integrases, and transposases. Resolvases and invertases (i.e. Tn3, gamma-delta, Tn5044 resolvases, Gin and Hin invertases) in this family contain a C-terminal DNA binding domain and comprise a major phylogenic group. Also included are phage- and bacterial-encoded recombinases such as phiC31 integrase, SpoIVCA excisionase, and Tn4451 TnpX transposase. These integrases and transposases have larger C-terminal domains compared to resolvases/invertases and are referred to as large serine recombinases. Also belonging to this family are proteins with N-terminal DNA binding domains similar to IS607- and IS1535-transposases from Helicobacter and Mycobacterium.	2.74991e-18
NZ_CP023992.1\|WP_069869001.1\|2010557_2011895_-\|M20/M25/M40-family-metallo-hydrolase	gnl\|CDD\|181163	PRK07906, PRK07906, hypothetical protein; Provisional.	0

>NZ_CP023992.1|WP_069869007.1|2000694_2001687_+|magnesium/cobalt-transporter-CorA
MRSVIVDCAIYRDGCRTEGPADFSDALDEARARGDAFLWIGLHEPTEKEFELVTSEFGLHPLAVEDALGAHQRPKLEVYDDSLFLVLKPVQYDDKAGTVTTGELMVFVGDSFVVTVRHGEANPLGSVRDRLEKMPEVLQHGPTAVMYAVSDAVVDHYLDVADDLHGDLEVLETEVFAPNAGGGQNTAGRIYAFKREVMEFRRSAGPLAEPMERLTGAGVPFVHEGSRPFFRDVSDHLTRVNEHVEGLDRLLSDILSAHLAQMGVRQNDDMRKISAWAAMAAVPTMIAGIYGMNFTHMPELEQPWGYPGVIVLMGGVIALLYRYFKRRGWL
>NZ_CP023992.1|WP_161370249.1|1999900_2000605_-|MSMEG_4193-family-putative-phosphomutase
MAAMPMLILVRHGRSTANTAGVLAGWTPGVALDERGTAQAAALPDRLARLPLAAAVTSPLQRCRETLAPLLAARPELPLHPDDRIGECHYGDWSGRKLAELADEPLMNIVQQHPSAAAFPGGESLRAMNARAVEAVRDWNARIEREHGADAAYLMCSHGDIIKALVADALGLHLDLFQRISVEPCSITAIRYTPTRPFLVRLGDTGDFAGLAPREETTGDRGGDAAVGGDAGAP
>NZ_CP023992.1|WP_069869009.1|1999186_1999777_-|DUF3090-domain-containing-protein
MSRQVFLYDPPDRFVAGTVGLPGRRTFFLQASAGSRTTSVALEKTQVAALAERIDELLDEVVRRTGGNAPVPAVAPTELSDTAPLEAPVEEEFRVGTMALAWDGEEQRMIVEAQALVELEAESEEDLAEAEERLLQDDVNGPPMLRVRLTGTQARAFAKRALEVVNAGRPPCPLCSLPLDPEGHVCPRQNGYRRGA
>NZ_CP023992.1|WP_099013155.1|1998239_1999088_-|SCO1664-family-protein
MAPSELLALGELTVRGRVREASNAVLYCTVEYEGHSAPCVYKPVAGERPLWDFPDGTLAQREVAAYEISEATGWGLVPPTVLRDGPYGQGMCQLWIEVEVTTGAADGDADGADGDGSGEAGGGELLALVEGDEPGPGWKAVGYAEVGEGRTALLVHADDVRLRRLAVLDAVINNGDRKGGHLLPAAGGRLYAIDHGVTFNADDKLRTLLWGWAGDPLPDDVLEVLRGLADQLADGGPLSARLAKLITEAEIEALRARVATLLRTGTHPEPSGQWPAIPWPPV
>NZ_CP023992.1|WP_099013154.1|1996814_1998044_-|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase
MYAWPASEVPALPGSGRDLSIHDTATGGRITLTPGPVARIYVCGITPYDATHMGHAATYNAFDLVQRVWLDTKRQVHYVQNVTDVDDPLLERAQENGDDWTALAERETALFREDMTALRMLPPRHYIGAVEAIPGIVPLVERLRDLGAAYELEGDVYFSVESDPSFGSVSRLDAEAMRLLSAERGGDPERPGKKNPLDPMLWMAARAGEPSWDGGSLGSGRPGWHIECVAIALDHLGMGFDVQGGGSDLAFPHHEMGASHAQVLTGERPFAKTYVHAGMVALDGEKMSKSKGNLVFVSALRRDGVDPAAIRLALLAHHYRSDWEWTDEVLREAEERLGRWRAAVSRPDGLPADALVEEIRKALADDLDSPAALAAVDRWAAAQTATGGTDEGAPGLVSRAVDALLGVAL
>NZ_CP023992.1|WP_099013153.1|1995548_1996697_+|PAC2-family-protein
MIELEGVPELIDPVMICAFEGWNDAGDAASTAVGHLDREWKGEVFASLDAEDYYDFQVNRPTVALEGGVRKITWPTTRLSVVRADTGEQSRDLVLVRGIEPSMRWRSFCNEILGYAHELGVEMVVILGALLGDTPHTRPVPVSGVTSDPDLARSLDLEETRYEGPTGIVGVLQEACAHAGVPAVSLWAAVPHYVSQPPNPKATLALLNRLEDLIGVRIPLGELTEDSRAWQLGVDQLAAEDSEVAEYVQSLEEARDTAELPEASGEAIAREFERYLRRRDGQPGPGGHATESGGLAEGREGGTSGGPGTPYLRDPSTGHGRPRKPSARDEMAKDDAEDTGGAEDETKGPDDAQEGEGQDASHREDGGTDRGGDGDEGSGSGR
>NZ_CP023992.1|WP_099013152.1|1993902_1995330_-|fuconate-dehydratase
MFSLAHRFREPPLSQRPSVTELEVHDIRFPTSEQLDGSDAMNPDPDYSAAYVVLRTDAGEGPAAEGHGFVFTIGRGNDVTAAAIRSLLPHVVGRPAPLTAADLAALHRELTHDSQLRWLGPEKGVMHMAAGAVVNAAWDLAARQAGKPLWRFLADMSPEELVGLVDFRYLSDALTRDEALAILRAAEPGRAERAALLRERGYPAYTTSPGWLGYSDEKMIKLAQEAVAEGFGQIKLKVGGDLDEDLRRMRLAREAVGPDVRIAVDANQRWDVAEAVRWMSALAPYDPHWIEEPTSPDDILAHAAIRAGQPVKVATGEHVANRVVFKQLLQAEAVDFVQIDAARVAGVNENLAILLLAAKYGLPVCPHAGGVGLCELVQHLAMFDFVAVSGSWEDRVIEYVDHLHEHFADPVVIESGRYRAPTAPGFSARMYPESIAAYRYPDGPEWRARIARPVPAPSASAPAPFTPAQPQEDHQ
>NZ_CP023992.1|WP_099013151.1|1993129_1993906_-|SDR-family-oxidoreductase
MTTGDFEGLAALVTGGASGIGAAIATTLRDRGARVAVLDRDPSGVPDGTLPLKADVTSDEAIRGAVAAAVAEFGALHTVVGNAGIGAIGSVEDNSDEEWHRLLDINVLGLVRTARAALPHLRAAAADRPGAVSITHTCSIAATAGLPQRAAYSASKGAVLSLTLAMAADHIREGVRVNCVNPGTVDTPWVGRLLGQAPDPAAERAALEARQPTGRLVSADEVAAAVAYLASPAAAAVTGTALAVDGGMQGLRPRPASS
>NZ_CP023992.1|WP_099013150.1|1991971_1993006_-|sugar-ABC-transporter-substrate-binding-protein
MTRLRTTGTAACAVLLAVAALTGCNRESNGAGGGKVGIDMPRTDTDFWNSYQQYLEKGIDKGTVSALPLSNSQNDISKLVANVQAFTDQGAKAIVMAPQDTGAISSTLEQLAEKKIPVVSVDTRPDSGKVYMVVRADNRAYGTKACEYLGEKLGGKGRVAELQGDLSSINGRDRSQAFASCMKKKYPGIKVHELPTDWKGDVASAKLQSLLAQHKDVNGIYMQAGGAFLQPTLALLEQKRLLKPAGSDKHITIISNDGIPEELDAIRSGKIDATLSQPADLYAQWALNYAKAALDGKSFKPGPTDHGSTIVKIENGLEDQLPAPLVTKENVDDKKLWANQLEKK
>NZ_CP023992.1|WP_099013149.1|1990373_1991969_-|sugar-ABC-transporter-ATP-binding-protein
MPAVDQPAVVRAQGIVKRFGPTVALDRARLAVRPGEAHALVGRNGAGKSTLVSVLTGMERPDEGEVTFGDEPAPGYGDTAAWQRKVACVYQKSMVVPDLTVAENLYLNRFPGAGRIRWRALRADARALLAEYGVEVDPQTRAKDLSVEQRQFVEIARALSFGARLIILDEPTAQLDAGGIDRLFAKLLELRRQGVAFLFISHHLQEVYELCDTVTVFRDARHVLTAPVAGLAKEDLVAAMTGDGGGAPGGDSGAAVHAPVARKAADPEGEPVLRTEGLALEGEFDPLDLVVRPGEVLGLAGATASGNTAVGETLVGLRKPAGGRLSVRGRPVRPGSVPHAIDAGIGYVPEDRHHQGLVLGRSVAENATLTVTDQLGPYGTVLPSRTRAFAQRMINSLDIKTSGPSQPVSGLSGGNQQKVVIARALAREPSVLVAIRPTAGVDVKSKDALLGVVREVAEAGSGAVIVSDELDDLRVCDRILAFFHGRVVAEFGGGWSDRQLVAAMEGITEPGTTGADGTAEDTEDRTEGRQP
>NZ_CP023992.1|WP_099016850.1|2001817_2002624_-|ferritin-like-domain-containing-protein
MLSAKSVFQEILDNDESFRLFCSVAASGEAQGGWENGRIAALVPESRRDLAPKIARHGIDEDKHGRIFNALLRKRGLEPMEVPRETDYTMLLEARGIGLAHDKLRRDEPLTDHDIVIYLAHSRVTEQRAAAQMTMLCRYFGDHPDLGRAVRMIADDEDNHLAYCHEELLRMAAAGYGRTIQRTLRESALVEMGVYRDVSLAVMARMGRVLGWSRAKSAPLAAGIRALYAYERLGGWRRMVSLRMPERRNALGGPEQSASGAPEAPELV
>NZ_CP023992.1|WP_069869006.1|2003121_2004171_-|LLM-class-F420-dependent-oxidoreductase
MRLGINLGYWGAGMDADNLAVAREADRLGYAVCWAAEAYGSDAATVLAWVAAQTERIDVGSAIFQIPARTPAMTAMTAATLDTLSGGRFRLGLGVSGPQVSEGWYGVRFDKPLARTREYVEIIRKAMSRERLSHEGQNWTLPLPDGPGKPLKLTVHPVREYIPLYIAAIGPKNLEQTGEIADGALVLFYAPEHAEATTLGSLRAGRAKVGKDLEGFDVVPTVPMALGDDVRALADQFRPYTALYVGGMGSAKQNFYNKLAQRLGYEKEAAEIQEKYLSGDKEGAAAAVPHDLIDSTALLGPVERIADRMQAYAEAGVTTLSLTPSGFTLEERLAGLRAGVEALERAGLA
>NZ_CP023992.1|WP_069869005.1|2004298_2005279_+|aldo/keto-reductase
MELRHLGRTGLRVSRLGLGTLTWGRDTDEHDAADQIKAFWEAGGTLVDTADVYADGGAEYLLGQLLEGLLPRRDLQIATKAGSVPDPDRRFDTSRGHLLAALDASLERLGTDYVDLWQVHAFDPFTPIEETLQALDIAVSSGRARYVGVSNFSGWQLAKAATWQLASSGAHTRLASTQMEYSLLQRGVEREVLPAALDLGVGLLPSSPLGRGVLTGKYRHTTPADSRGASELAAFVAPYLDEEASRIVEAVAIAADGLATTALNVALAWVRDRPGVTAPIVGARNAQQLRAALSAESLSLPDEICQALDDVSAPVHRYPDQDWSTL
>NZ_CP023992.1|WP_099016851.1|2005443_2007894_+|hypothetical-protein
MDPERAPDGDHGEPGAGGAPAGADRDDTGAVAAERDGAVGLTAGGDHSDQSSTNEADGPVTGAQAPSAGHGGTSGGPGVDPGGAGDAEEHPAEAGTGMGPGGSAPAAPGEPGDAQAPAEAGPRGVQGGQGRRSAAAEALAAAVRAVESGERSAASFFNDAPAPRPAAPAAPARERARAAAPASAPAPVRPPSARPAPGPGGEIPGSGDVRQVLAAGGAPETLAGRVAEVLGERAAEALREDPWQLLAVPGVRPDQADGFARALLGPDCEPGDERRALALTSWLLERAALEGHTALESSALREALAKVSVPDPDEALRTAIAEGVVLVFQDALDAAPGARPRAAEDEDAEQPVRVLLGLDRYALAEESLADGLARLASTFASPQGGAADGEAPAGDPGAPGWESAAATAPTASAAELIRTAAAHGLVAHSGGEAARAEPVALVAAARAMGLRAYVAAHSEDGRRRLAASLSEAASGGRSAAPDSDPDTGPDADPETASAAVTVAGLLADAEGPGRDEEGTLALDLLAVLDAPQLDVETAAMLVESLPDGARLVLSGDPGVLWSAGPGRVFADLVAARRCPQVVSRTPDPGPIGELISGIGIGELNQVEAPGKEVVIVPVRDAGEAVHRTVQLVADSVPRAIGIPPEQTQVITPGHGGAAGTRALNAALKDRLNPGPGRFGGFDPGDRVAYSPAPGRTVPGTVVSADAEGLRLDCAGAPVVVERAEVGELVRHGWALTAHQAAGARWPAAVVVLPGDATAGLTRAWVYTAFGRGERHLSVVHGAESALPKAVAEIPFKDRTTRLRALLQAQTPTAPTD
>NZ_CP023992.1|WP_079257036.1|2008214_2008889_-|hypothetical-protein
MSDAAQPSAAEVRAAAEAVKAALDRHLDAVERRSGEGDPAVYAAFNELAAAAEVYDELLYDAYDEVTPFEIPGDDRLPAYAGPEEPSALSVLIRRDYVVAEPQRLLSQAQRIADLDPDIDTGNGREGGGAAAGESVHTALGVVFGEFEPDEIASRHKEFGLEEGDSTLWVVAAEEPPEPGEWLSAPFDQADPHMVVCRFDMSSVFDEELEDEDEDDLEVLEPGS
>NZ_CP023992.1|WP_014059547.1|2008936_2009125_+|hypothetical-protein
MPEYEFCDVYVPRGVSRKATTRLLTDHAEYGHWELDRLRLNPDGSRRVRLRRRIIRQLRATW
>NZ_CP023992.1|WP_099013156.1|2009336_2010230_-|chaplin
MRQVAKKGLITVAAASGVLAVTGGYAQAAGSGADGGAMYSPGIVSGNNIQAPVHVPVNLCGNTVSVIGVLNGAGGGQCGGGSGDSSGGGAQSGGSQAQGVASGSSGIGSGNNIQAPIGVPVNVCGNNISAVGFGNSSDGGECGETVPAVPENPSEPGEPGEPGNPGEPGNPGEPGEPGNPGNPGQPGNPGNPGNPGNPGEPGNPGNPGNPGNPGQPGNPGNPGGSNPGGGSNQPGHSSPGHQTEHTGVHGVDPSANLGGKEQLAQTGAGPVALAIPAAAGMLLAGTVLYRRARAAQH
>NZ_CP023992.1|WP_069869001.1|2010557_2011895_-|M20/M25/M40-family-metallo-hydrolase
MSESLSGATTTGTVRGEDEVVDLCRDLIRIDTSNYGDHSGPGERAAAEYVAEKLAEVGLEPKIFESHKGRASTVARIEGEDPSRPALLIHGHTDVVPANAEDWTHHPFSGEIADDCVWGRGAVDMKDMDAMTLAVVRDRLRSGRKPPRDIVLAFLADEEAGGVYGARHLVDNHPGLFEGVTEAIGEVGGFSFTVNEQLRLYLIETAQKGMHWMRLTVDGTAGHGSMTNNDNAITELSEAVGRLGRHKFPVRVTKTVRSFLDELSDALGTPLDPENMDETLAKLGGIAKIIGATLQNTAAPTMLNAGYKVNVIPGQATAHVDGRFLPGLEDEFLADLDRILGPRVKREDVHADKALETSFDGALVDAMQSALKAEDPIARAVPYCLSGGTDAKSFDDLGIRCFGFAPLRLPPELDFAGMFHGVDERVPVDGLKFGVRVLDRFLDAC
>NZ_CP023992.1|WP_099013157.1|2012176_2013862_-|recombinase-family-protein
MPRFAFAGRCSTEDLQDPETSRNWQLTRARALIEPAGGEIVAEYFDSGHSRALPWKRRPQAAALLTALRDPHRGFDAVVIGEPQRTFYGNQFGNTFPLFTHFNVPLWVPEIGGPIDPDNEAHDLVMSVFGGMSKGERNRIKIRVRTAMGSQAKIEGRFLGGRPPYGYRLTDAGPHPNPAKAADGKRLHRLEPDPDTAWVVVRTFTEYLEGKGYYAIAEGLTRDGIPCPSAYDRDRNRHRKGHAWCKGAVRAILVNPRYTGHEVWSKQRKDEVLLDIDDVTLGHRTKMAWNTPEQWIWSAQPVHQPLISPTTFAHAQAKRHARSTQTHLERKPRPTTRGYALRGLIRCAICQRKMQGTFNNGKPHYRCRYNAEYAKNAALDHPLTVYVREEVILPELDKWIAKAFAPGQLTATLQAMRQAQSAESPTTTAAAAARRTMAECDRRIVQYRAALDAGTDPKLATEWINQAQSEKASARQDLLTATAIQPEILTEDQIKHMVSGLGSMTDRLLTTASEHKRPLYESFGLALTLDMQKRVVIVESQPAHTCTYGKCPRGDLNPHAR
>NZ_CP023992.1|WP_099013158.1|2014197_2015139_-|RNA-methyltransferase
MSDRESVWNTAPTSAHAQRADRYVSGSNAHPAKMLPAIAAHAIRTYTKPGELVLDPMCGIGTTLVEAIHHRRHALGIEYESRWARIARANIAHNIRHVEQCSGRVVCGDARQLTQLIDADLHGKVALVVTSPPYGPSAHGRVHCTSETGERGVVKTDYRYGRDPHNLAHVSTDQLLDGFSKILTQCRTVLRPGGTVVVTTRPWRTHGELIDLPSAVLATGQAAGLVPTERCVALLAGIRDGRLIARPSFFQLKNVRDARRQGIPLHLVQHEDVLIFTRPEKPSAMSQPLCTRHERQAGTSRCGYPRSHRKTRL

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Crispr_ID: NZ_CP023992_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_2

2664594-2664680

Orphan

Consensus_repeat	Method
CAGACTCCCGCCGGGCCCGGCTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_2

>merge|NZ_CP023992|2|2664594-2664680|CRISPRCasFinder
CAGACTCCCGCCGGGCCCGGCTCAGGCTTCCGCCGGCCCGGCTCAGGCTCCCCCAGGCCCGGCTCAGGCTCCCGCCGGGCCCGGCTC

>NZ_CP023992|2|2|2664594-2664680|CRISPRCasFinder
CAGACTCCCGCCGGGCCCGGCTC	AGGCTTCCGCCGGCCCGGCTCAGGCTCCCCCAGGCCCGGCT
CAGGCTCCCGCCGGGCCCGGCTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_099013442.1\|2660263_2662696_+\|transglutaminase-domain-containing-protein	unknown	unknown	gnl\|CDD\|376628
NZ_CP023992.1\|WP_069870186.1\|2657059_2657614_+\|carbonic-anhydrase	unknown	unknown	gnl\|CDD\|239474
NZ_CP023992.1\|WP_099013448.1\|2669352_2670909_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224154
NZ_CP023992.1\|WP_099013441.1\|2658899_2660267_+\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP023992.1\|WP_069870214.1\|2674341_2674707_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|375793
NZ_CP023992.1\|WP_099013451.1\|2674820_2676074_-\|oxidoreductase	unknown	unknown	gnl\|CDD\|369639
NZ_CP023992.1\|WP_099013444.1\|2663582_2664365_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|182918
NZ_CP023992.1\|WP_099016884.1\|2652887_2654870_-\|penicillin-binding-protein-2	unknown	unknown	gnl\|CDD\|223839
NZ_CP023992.1\|WP_079257291.1\|2672190_2673108_-\|methylenetetrahydrofolate-reductase-[NAD(P)H]	unknown	unknown	gnl\|CDD\|366988
NZ_CP023992.1\|WP_069870204.1\|2668328_2668949_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP023992.1\|WP_099013450.1\|2673455_2674109_-\|thiamine-phosphate-synthase	unknown	unknown	gnl\|CDD\|234590
NZ_CP023992.1\|WP_079257285.1\|2655686_2656649_-\|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH	unknown	unknown	gnl\|CDD\|234597
NZ_CP023992.1\|WP_099013446.1\|2665244_2666237_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP023992.1\|WP_099013447.1\|2666208_2668293_+\|YhgE/Pip-domain-containing-protein	unknown	unknown	gnl\|CDD\|274414
NZ_CP023992.1\|WP_093703451.1\|2657826_2658879_+\|MoxR-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP023992.1\|WP_099013449.1\|2671112_2672123_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236090
NZ_CP023992.1\|WP_147968123.1\|2654866_2655058_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013443.1\|2662915_2663311_-\|DUF3040-domain-containing-protein	unknown	unknown	gnl\|CDD\|378610
NZ_CP023992.1\|WP_099013440.1\|2655066_2655690_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237030
NZ_CP023992.1\|WP_099016885.1\|2676759_2677947_+\|glycine-oxidase-ThiO	unknown	unknown	gnl\|CDD\|274092

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_099013442.1\|2660263_2662696_+\|transglutaminase-domain-containing-protein	gnl\|CDD\|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.67014e-23
NZ_CP023992.1\|WP_069870186.1\|2657059_2657614_+\|carbonic-anhydrase	gnl\|CDD\|239474	cd03379, beta_CA_cladeD, Carbonic anhydrases (CA) are zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide in a two-step mechanism in which the nucleophilic attack of a zinc-bound hydroxide ion on carbon dioxide is followed by the regeneration of an active site by ionization of the zinc-bound water molecule and removal of a proton from the active site. CAs are ubiquitous enzymes involved in fundamental processes like photosynthesis, respiration, pH homeostasis and ion transport. There are three evolutionarily distinct families of CAs (the alpha-, beta-, and gamma-CAs) which show no significant sequence identity or structural similarity. Within the beta-CA family there are four evolutionarily distinct clades (A through D). The beta-CAs are multimeric enzymes (forming dimers,tetramers,hexamers and octamers) which are present in higher plants, algae, fungi, archaea and prokaryotes.	4.72035e-59
NZ_CP023992.1\|WP_099013448.1\|2669352_2670909_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|224154	COG1233, COG1233, Phytoene dehydrogenase and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	8.78558e-65
NZ_CP023992.1\|WP_099013441.1\|2658899_2660267_+\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	8.42354e-30
NZ_CP023992.1\|WP_069870214.1\|2674341_2674707_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|375793	pfam18367, Rv2175c_C, Rv2175c C-terminal domain of unknown function. This is the C-terminal domain of unknown function found in actinomycetes such as M. tuberculosis Rv2175c. Rv2175c has a DNA binding activity and possesses a winged helix-turn-helix fold, furthermore it is identified as a substrate of the PknL kinase.	1.15465e-29
NZ_CP023992.1\|WP_099013451.1\|2674820_2676074_-\|oxidoreductase	gnl\|CDD\|369639	pfam07992, Pyr_redox_2, Pyridine nucleotide-disulphide oxidoreductase. This family includes both class I and class II oxidoreductases and also NADH oxidases and peroxidases. This domain is actually a small NADH binding domain within a larger FAD binding domain.	4.3271e-53
NZ_CP023992.1\|WP_099013444.1\|2663582_2664365_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|182918	PRK11036, PRK11036, tRNA uridine 5-oxyacetic acid(34) methyltransferase CmoM.	2.43438e-24
NZ_CP023992.1\|WP_099016884.1\|2652887_2654870_-\|penicillin-binding-protein-2	gnl\|CDD\|223839	COG0768, FtsI, Cell division protein FtsI/penicillin-binding protein 2 [Cell envelope biogenesis, outer membrane].	3.46285e-132
NZ_CP023992.1\|WP_079257291.1\|2672190_2673108_-\|methylenetetrahydrofolate-reductase-[NAD(P)H]	gnl\|CDD\|366988	pfam02219, MTHFR, Methylenetetrahydrofolate reductase. This family includes the 5,10-methylenetetrahydrofolate reductase EC:1.7.99.5 from bacteria and methylenetetrahydrofolate reductase EC: 1.5.1.20 from eukaryotes. The structure for this domain is known to be a TIM barrel.	7.77771e-141
NZ_CP023992.1\|WP_069870204.1\|2668328_2668949_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.68941e-15
NZ_CP023992.1\|WP_099013450.1\|2673455_2674109_-\|thiamine-phosphate-synthase	gnl\|CDD\|234590	PRK00043, thiE, thiamine phosphate synthase.	4.03982e-86
NZ_CP023992.1\|WP_079257285.1\|2655686_2656649_-\|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH	gnl\|CDD\|234597	PRK00050, PRK00050, 16S rRNA (cytosine(1402)-N(4))-methyltransferase RsmH.	6.96915e-156
NZ_CP023992.1\|WP_099013446.1\|2665244_2666237_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	4.74712e-19
NZ_CP023992.1\|WP_099013447.1\|2666208_2668293_+\|YhgE/Pip-domain-containing-protein	gnl\|CDD\|274414	TIGR03062, hypothetical_protein_lp_1332, YhgE/Pip C-terminal domain. This family contains the C-terminal domain of a family of multiple membrane-spanning proteins of Gram-positive bacteria. One member was shown to be a host protein essential for phage infection, so many members of this family are called "phage infection protein". A separate model, TIGR03061, represents the conserved N-terminal domain. The domains are separated by regions highly variable in both length and sequence, often containing extended heptad repeats as described in model TIGR03057.	9.41978e-90
NZ_CP023992.1\|WP_093703451.1\|2657826_2658879_+\|MoxR-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	2.6896e-97
NZ_CP023992.1\|WP_099013449.1\|2671112_2672123_-\|hypothetical-protein	gnl\|CDD\|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	0.000206885
NZ_CP023992.1\|WP_099013443.1\|2662915_2663311_-\|DUF3040-domain-containing-protein	gnl\|CDD\|378610	pfam11239, DUF3040, Protein of unknown function (DUF3040). Some members in this family of proteins with unknown function are annotated as membrane proteins however this cannot be confirmed.	1.55437e-30
NZ_CP023992.1\|WP_099013440.1\|2655066_2655690_-\|hypothetical-protein	gnl\|CDD\|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.15043e-06
NZ_CP023992.1\|WP_099016885.1\|2676759_2677947_+\|glycine-oxidase-ThiO	gnl\|CDD\|274092	TIGR02352, Glycine_oxidase, glycine oxidase ThiO. This family consists of the homotetrameric, FAD-dependent glycine oxidase ThiO, from species such as Bacillus subtilis that use glycine in thiamine biosynthesis. In general, members of this family will not be found in species such as E. coli that instead use tyrosine and the ThiH protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Thiamine].	3.81445e-124

>NZ_CP023992.1|WP_099013444.1|2663582_2664365_-|methyltransferase-domain-containing-protein
MSDPQRPRASLRTAVVWEVLKDALERRAKATGREAVGGEAVHGALDVLDTGGGSGNFAVPVARLGHHVTVVDPSPNALFALERRAAEAGVADRVRGVQGDAHGLFDVAERGGYDVVLCHGVLEYVDDPAEGLRNAAAALRPAGTLSLLAAGLGGAVLARALAGHFTEARQALTDPEGRWGSGDPIPRRFTADQLSELVTAAGLEIAAVHGVRVFADLVPGVLVDTEPGALDALLQLEEAAAELPAFRSVATQLHVLAERD
>NZ_CP023992.1|WP_099013443.1|2662915_2663311_-|DUF3040-domain-containing-protein
MPLSEHEQRMLEQMERALYAEDPKFATALEGSGLRTYTRRRVYQAVAGFLVGIALLMVGVIVPQIWISVVGFLIMLGCAVLAVTGWRKAPKPGEAQQGGGGAAPRRQGRQRRSMMTRIEQRWQRRRDEQGH
>NZ_CP023992.1|WP_099013442.1|2660263_2662696_+|transglutaminase-domain-containing-protein
MSGSVRLAICAALATVAAACALLPLVDPASWLLQAVLLLAIQSATGVAVRRVPLARPLTVVAQAVVTLLLLTLVFAHDQALGGVLPSPQALHEFALLLRDGADDVGQYAIPAPLTDGIRLMLVGGVMAIGLVVDALAVTYRSAAPAGLPLLALYSVAAGLSDDGSDWLWFLLAAAGYLLLLLAEGRDRLSQWGRVFSGGAPHPSGMPPSGLAGAGGSPALAPVRTGRRIGVLALGIALAVPAVLPSLDGGLLDRQGGAGGAGSGGGTISAVNPLVSLQDSLNQPENKEVLRYRTSSQTTQDLYLRIVALDRFDGTSWKSSERHVTDVPDQLPSPSGLGPSVQVSSIDTSISAADWYAQNWLPLPYPASKVEIDGRWRYEPEGRTLVGDRGQTTRGARYRVTSLLVEPTAEQLADAPAAPSRLRSEYTKVPDSLPSVVARTARGVTAGASNAYEKAVKLQDWFAVSGGFRYDTQVQSGSGSAAIVRFLKQREGFCVHFSFSMAAMARTLGIPARVAVGFTPGTAQADGTVSVGLKDAHAWPELYFEGVGWTRFEPTPSRGTQPDYTMEQTPSGTPTDEPTTEPSETSEPSAAPTASDSCSPEMKKLGTCGGAAAQQPDNGASGGGWSATKVTSWSSLAVLLLVVPLLPMLWRRRIRTRRLDGSGGRTEQDATDRILAAWRELTDSAWDFGVMPDDSLTSRRAVARMVRIAGLDDEPAQAAQRVATAVEQVLYAPHPRPAAGVADDVRLVVAGLRAKAGRRERLRALLAPRSAAQVAWAAGQRWSALVERWGAPRWARWAAQLRTPRGEQES
>NZ_CP023992.1|WP_099013441.1|2658899_2660267_+|DUF58-domain-containing-protein
MGPEGPGADERSGGLRAALAGLTTRGRSFLAAGMAAAVCSYVLGQADLLRVGLLLAALPLVCVAVVHRTRYRVAGSRRLAPARVPAGSEARVHLRMDNVSRLPTGLLMLQDRVPYVLGPRPRFVLDRVEPGGRREVSYRVRSDLRGRYPLGPLQLRLSDPFGMCELTRAFSAYDTLTVVPRVEPLPPVRLTGEAAGYGDGRHRSLALAGEDDVIPRGYRVGDDLRRVHWRSTARYGELMVRREEQPQRAHCTVLLDTRRTAHYGSGPDSAFEWAVSGAASAAVHLLERGYAVRLLTDTGSSVPGPDGGGGFAGSTHDSAETAGLMLDTLAVVDHSDSGGLSPAFEVLRGGGEGLLVAFLGDLDEEQAATAARMRHRTTAAVAFVLDGAAWSRGAEFGGTQELEERLRRLREAGWTALPVGPGASLAQLWREADAQGATRADAGGPAVGGMTGSWT
>NZ_CP023992.1|WP_093703451.1|2657826_2658879_+|MoxR-family-ATPase
MTTYDERASLSDLTTTAERIRRSVESVIEGKPEVVRLSLTVLLAEGHLLIEDVPGVGKTMLAKALARSIDCSVRRIQFTPDLLPSDITGVSIFDQQRKEFEFKPGAIFAQIVIGDEINRASPKTQSALLESMEERQVTIDGESYELPDPFMVVATQNPVEMEGTYPLPEAQRDRFMARVSIGYPSPQAELQMLDVHGGVSPLDDMQPVAHAHEIVKLVEAVRSVHVAEAVRRYAVDLVAATRNHPDLRLGASPRATLHLLRAAKASAALAGRDFALPDDVQSLAVAVLAHRLLPTAQAQLNRRTSEQVVTDIIQRTPVPTSGPRGTGGMPPMPPMPPADYGRPQPGARRL
>NZ_CP023992.1|WP_069870186.1|2657059_2657614_+|carbonic-anhydrase
MSISAPQPNPSTDRDARTGDTVTDRLVAANRKYAEQFADPGMDARPVRRVAVVACMDARLDLHEALGLELGDCHTIRNAGGVVTDDIIRSLTISQRALGTRSVVLIHHTGCGLLNLTEDFRHELEEEVGQRPPWAVEAFRDLDADVRQSMQRVRTSPFLLHTDDVRGFVFDVTTGLLREVTPRR
>NZ_CP023992.1|WP_079257285.1|2655686_2656649_-|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH
MSSNALHVPVMLQRCLDMLAPALAQPGAVVVDCTLGLGGHSEALLRDFPEARLIALDRDPSALRLAGERLAPYGDRATLVHAVYDELPEVLDRLGVPRVQGILFDLGVSSMQLDEAERGFAYAQDAPLDMRMDQTTGVSAAEVLNTYPPGELVRILRAYGEEKFAKKIVDAVVRERAKEPFTNSARLVELIRDALPQAAKRTGGNPAKRTFQALRIEVNGELAVLERAIPAAVRTLAVGGRIAVLSYHSLEDRLVKQVFAAGAGDTAPPGLPVIPERYQPRLKLLTRGAELPTEEEIAENRRATPARFRGAERIREEVGP
>NZ_CP023992.1|WP_099013440.1|2655066_2655690_-|hypothetical-protein
MSVRGTRPKGRPVPGATPARRTPFVLLVVVLLGSGLIALLLLNSSLNQGSFELSKLEKQTNELTDERQALQQDVDKLSAPAELERRARQLGMVPGGNPVFLNPDGSVSGVPAPVTGQPSVLGAPGAVLPSAPDPAPSEAASTRYGSSPTPSVLAPPAPPTATPSGAGAGTASATPSVTPWAPPTGVSASASHSASVSAPAEATPDPQ
>NZ_CP023992.1|WP_147968123.1|2654866_2655058_-|hypothetical-protein
MTRSPARAQPGPPARTTARAPWRAAEPWTAAAGPATATRPRAATEPGLTTGPGTATEQTAAVA
>NZ_CP023992.1|WP_099016884.1|2652887_2654870_-|penicillin-binding-protein-2
MTAPRDPRRRGVPGPAGPRGDRRPRQAAARRPGERQGGSSGRPARRPRPGGPPVLRLGSPRPRLRLISLGLTLVMLIFVVRLLQVQAVDASAYSAKANVNRYIPVKLSAERGSITDRNGVDLATTVDAYDITAAPDLLAPKTAKTRDAPRQAAALLAPILGKEPADLEKKLTDNPASQYVVLARQQSPQVWNQIKDLKSALDDAAAKGKGTNVLAGVNREAHSKRVYPNGDLAAGILGFVDADGRGAAGLEQQLDKKLGGKDGKRVYAQSGGHQVPTGDVKEQPAVPGSDFELTIDRDIQWAAQSAIADQVRKSGADRGYVIVQDTRTGQLLALANAPGFDPNDITTTNADALGNAAVSDAYEPGSVSKLMSMAAVLQEGVARWDTHVVVPNRLPRADRAFADDIDHQTWYLTLNGVLAKSSNIGTILATEQLGKTKAEKNQILYSYLRKFGIGRPTGLGFPGETPGILARPQDWSASQQYTIPFGQGLSLNAVQAASVYSTIANGGERIAPTLVRGSRGPDGDFTAASAPEKTRVVSKETAKTLAEMLESVVDDQQGTGTKAKIPGYLVAGKTGTSNRVDPKTGRYRGYTASFAGFAPADKPRLTVYCAVQNPTKGSYFGGQVCGPVYKKVMEFGLKALQVPPSGKQPKRLPVSYNPGQ
>NZ_CP023992.1|WP_099013446.1|2665244_2666237_+|ATP-binding-cassette-domain-containing-protein
MGPSWGTPLTIGSDQRERPRHRTPLHHAAYCFCTDQSVQKPKEVICVGGTPEAESGAAVTAGGLGVKGPHGWAFRGAGIAADPGSLIAIEGPSGSGRTALLLTLTGRMRPTEGHGRVGDFRVPQQMARIRRISALAHVPGVAELDPVLTVAEHLRERALLRRRFTDSPRGLLRPRRERAAASRAVIDAALTAAGLDPDTLPKGPRTAVRDLERLEALRLSIALALVARPRLLGIDDADMKLSDAERERVWALLREIAESGTTVLAVCSQAPAGAVVVRTGRTSAADDGDEKTQQPRKTDADTVGTPTADDNRHDENEEGAADALAETRRA
>NZ_CP023992.1|WP_099013447.1|2666208_2668293_+|YhgE/Pip-domain-containing-protein
MRSPKLAALELKRFGRGRLPRAALAALLLLPLLYGALYLWSFWDPYGKLDKIPVALVNSDTGATVRGEHLTAGDDITGELLDSKTFDWHPTSAAEARKGVANGTYYLSLTVPSDFSRQIASSSGKSPETGALKVRTNDANNYIVGQISRSVFSEVRAAASAKASRGFYDNIFISFADIHGETAKAAKSADKLGKGIGKAKKGADDLAKGLAKAKEGSRDLKSGLGTLYKGSGTLKTGAGGVADGTQSLSDKVNDVAAKVRPFLKEHGKEIGDVSQLVADASRKASDNLDTLPETTATAATKARKASDDLAADHRARCEGAVPAGPDCPALKKSVAAAGTAADVAEDVNQLVKDHTTELDALGGHLDDLHDQAVWLAHNAPHLDTDLDTAVRKVNALNSGAQKVAEGAGTLHTGLNTAKTGASDLDSGVGKARGGADTLGGGMYRLVDGSGKLSGGLHDGAAKIPDYGEQDRDDRTEVMSDPVRLVNQAVHKAPNYGTGFAPYFIPLSLWVGAMVAYMLIQPLNGRALAVGASSWRIAFAGWLPVAAIGVLQTLALMAVLHWAIGLQMVRAAGTLGFLMLVTACFAAIVQWLNARFGPAGRILVLALLMLQLTSAGGTYPVQTSPGFFNAIHPFLPMSYVVDGLRRLITGGGLGPVWPACGVLLGYTAAALALTAWTARRRQVWSLNRLHPELSL
>NZ_CP023992.1|WP_069870204.1|2668328_2668949_+|TetR/AcrR-family-transcriptional-regulator
MDSSSTRRQATRQKLFEAAVTLIAEQGFSSTTVDEIAERAGVAKGTVYYNFASKTVLFEELLQHGIELLTASLQSAADENAERGGSHVDALDAMVRAGLDFISRYPSLTQLYVAELWRTNRAWQSTLMMVRQRAIAVIESELRAGVAAHEFSGDIDIPLTASALFGMVLVAALDWQSYQPERSLEDVHAALSRLLQGRVGGTVASG
>NZ_CP023992.1|WP_099013448.1|2669352_2670909_+|NAD(P)/FAD-dependent-oxidoreductase
MARIVVIGSGMGAMAAAARLAVAGHRVVVYERGRTHGGGVGRFARDGFRFDTGPGLLHLPAVYRDLFVKTGKQTLEQSVELVQVDPASRHLFADGTDFRLPNASRAGVLQALDGAFGAGAGERWSDLVNRAREVWDATRRPLLEEPLRADWRVLGRDPYPAAPVRRGRLGGLFGRGRADGPRTLAEVARRELKDPRAAALLESHALAHGLDPRSAPAAATVLPYIEQTFGTWYVGGGMRALADALHERCRRRKVEFHFEAEVTGIVEKDGRAAGVELADGTVAEADVVVSGIDPALLPPLLGGQEPWREDDVRPEPDPGGGTPGRLTVFLALSGARPEDAAHRTVVHAPDREAELTAVFGDGPGLREPCPRPTVTVLRPDDPAVRPDEDHEAVTLTAVVAPHDPVDWTDGTAAEQDAQRLITAAEAAIPGLRDRLLWHEVRTPADTGTETGARGGGVPGPALAGADGAFLRPANVTRLPGLYLAGGWAHPGGGLAHAGMSGALVAGLIVEGEDWRGSQ
>NZ_CP023992.1|WP_099013449.1|2671112_2672123_-|hypothetical-protein
MGWTVLYIAFGVVALWLLGEVLLQYKARLRWRLLAFVGFLGVVGGVLIPSVPVIGVGAIAFAIGQTYVTLSFRRGFAAGWALSGGLPGLLGREERGARPDGVDKEPILEVSDLEAVPAAQPEPPTYQPQPEPPTYQPQPMPDETGEYGVYEEPSPFTPASGEYSDAAAAGYSAYETYGGYGSQQDHSQGQGQNYGQDVYADQMGQAGQYGYGNEAYAAYGQDPYGGAQPQPQPYDQQVYGQQQYEQQQYADQYSAYGQQDPYGGGAAYGGDHWAADASYPSPDQGYDVMQSGGPWVPQQREGDAAPAADQQAYPYQQQHQGQGQGYPQGFDEQYRY
>NZ_CP023992.1|WP_079257291.1|2672190_2673108_-|methylenetetrahydrofolate-reductase-[NAD(P)H]
MALGTASTRTDRARTVRDLLASGEQSYSFEFFAPKTAKGEQTLWNAIRRLEAVSPTFVSVTYGAGGSSREGTVRVTERIATDTTLTPVAHLTAVNHSRAELRNIIGQYAGAGIRNMLALRGDPPGDPMGEWISHPDGLDYAAELVRLIKESGDFCVGVAAFPEMHPRSTDWDTDIGHFIDKCRAGADFAITQMFFYPEDYLRLRDRVAAAGCTTPIIPEIMPVTNVKQIERFAQLSNAAFPPELAERILAVKDDPAAVRSIGIDYATELCARLMAEEIPGLHFITLNHSPATLEIYENLGLHQRS
>NZ_CP023992.1|WP_099013450.1|2673455_2674109_-|thiamine-phosphate-synthase
MSTTATAHEQLADARLYLCTGARKRQGDLPEFLDAVLGAGVDIVQLRDKEMEAAEELEHLRVFADACRRHGKLLAVNDRADVAHAIGSDVLHLGQGDLPVPAARAILGEDVLIGRSTHAEAEVDAAAVQPGVDYFCTGPCWPTPTKPGRPAPGLPLVRHAAALGTDRPWFAIGGIDASNLDQVLEAGARRIVVVRAITAADDPAAATADLAKRVRAV
>NZ_CP023992.1|WP_069870214.1|2674341_2674707_-|helix-turn-helix-domain-containing-protein
MTEIDAKIDALVPAWLTLPDVAERLGVEVTRVRQLVKEGQLIAVRRGENRVLQVPEEFIGEGRVVKGLVGTLTLLKDDGFSDEEMLEWLFTPDPSLPGTPAQALSENRGTEVKRRAQALAV
>NZ_CP023992.1|WP_099013451.1|2674820_2676074_-|oxidoreductase
MSDETTTKPSSNGGEQRVVIVGAGMAGVQTAVALREQGWTDEIVLLGAEVHQPYDRPPLSKAVLLGKAEGSTLDVDFAGLGIGLRLGVEVTGLRTDKRLVETATGQLPYDVLVLATGAEPIPLPGGEGVPGVHLLRTLDDATRLRPVLARQREIAVVGAGWIGAEFATAAREAGCAVTVVEAADRPLAGALPAEVAAPMAAWYEDYGARLVTGARVASVDEAGLVLGDGTRLRAGAVVVGIGARPATGWLAGSGVELSGDRSVAADERLRASAPDVYAVGDCASFPSARYGSRLLVHHWDNALQGPRTVAANVVGSRTAAHFPGVVYDPVPYFWSEQFGRFVQYAGHHAGADELVWRGDPAGAAWSVCWLREGALVALLAVGRPRDLAQGRKLIERGARLDRTRAEDPSVPLKSAVL
>NZ_CP023992.1|WP_099016885.1|2676759_2677947_+|glycine-oxidase-ThiO
MGGGIVGLVTAWRAAQRGVRIALADPEPGGGAAWVAAGMLAAVTELHYGEQTLLGLNMASARRYPDFVAELEEASGQDVGYRACGTLAVAFDADDRAHLRELHTFQQGLGLESEWLTGRECRRLEPMLAPGVHGGLRVAGDHQVDPRRLTAALLTACERAGVAFHRARVERLLVDGDRATGVELTGGVRLAAERTVLAAGSLSGRLAGVPDDVLPPVRPVKGQVMRLSVPERYAPFLSRTVRAVVRGGPVYLVPRENGELVIGATSEELGWDTTVTAGGVYELLRDAHEVVPGITELPLVETCAGLRPGSPDNAPMLGPTALPGLLLATGHFRNGVLLTPITGDVMAEALTSGELPPEAQPFTPRRFTAPSGAGAAPTVSAVPAAAPSPAQEQQT

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Crispr_ID: NZ_CP023992_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_3

2765977-2766080

Orphan

Consensus_repeat	Method
CCGAAGCCACCGCCGAAGTCGCC	CRISPRCasFinder

2 spacers

csa3

The CRISPR arrays of NZ_CP023992_3

>merge|NZ_CP023992|3|2765977-2766080|CRISPRCasFinder
CCGAAGCCTCCCCCGAAGCCACCGCCGAAGTCGCCACCGTTCCCGAAGCCACCGCCGAAGTCGCCGCCGTTCCCGGAGTCGCCGTAGCCACCGCCGAAGTCGCC

>NZ_CP023992|3|3|2765977-2766080|CRISPRCasFinder
CCGAAGCCTCCCCCGAAGCCACC	GCCGAAGTCGCCACCGTTC
CCGAAGCCACCGCCGAAGTCGCC	GCCGTTCCCGGAGTCG
CCGTAGCCACCGCCGAAGTCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_020871972.1\|2761690_2761888_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069869288.1\|2776671_2778030_-\|MHS-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340927
NZ_CP023992.1\|WP_069869392.1\|2759281_2760097_+\|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl\|CDD\|184638
NZ_CP023992.1\|WP_069869294.1\|2771933_2772443_-\|inorganic-diphosphatase	unknown	unknown	gnl\|CDD\|376376
NZ_CP023992.1\|WP_099013485.1\|2773350_2774406_+\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176234
NZ_CP023992.1\|WP_099013487.1\|2775196_2775586_-\|cupin	unknown	unknown	gnl\|CDD\|380437
NZ_CP023992.1\|WP_069869300.1\|2761898_2762579_+\|DUF4191-domain-containing-protein	unknown	unknown	gnl\|CDD\|379389
NZ_CP023992.1\|WP_069869289.1\|2775582_2776392_-\|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|143605
NZ_CP023992.1\|WP_069869297.1\|2765001_2765592_-\|Ig-like-domain-repeat-protein	unknown	unknown	gnl\|CDD\|379864
NZ_CP023992.1\|WP_079260419.1\|2769062_2769701_-\|LysE-family-translocator	unknown	unknown	gnl\|CDD\|224199
NZ_CP023992.1\|WP_099013483.1\|2767460_2768678_-\|Ig-like-domain-repeat-protein	unknown	unknown	gnl\|CDD\|379864
NZ_CP023992.1\|WP_099013480.1\|2762775_2763243_-\|RDD-family-protein	unknown	unknown	gnl\|CDD\|377640
NZ_CP023992.1\|WP_069869301.1\|2760403_2761354_+\|lipoyl-synthase	unknown	unknown	gnl\|CDD\|235493
NZ_CP023992.1\|WP_069869298.1\|2763497_2764907_+\|type-I-glutamate--ammonia-ligase	unknown	unknown	gnl\|CDD\|273198
NZ_CP023992.1\|WP_099013477.1\|2754995_2756339_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|366721
NZ_CP023992.1\|WP_099013484.1\|2772526_2773231_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379115
NZ_CP023992.1\|WP_099013478.1\|2756593_2757358_+\|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|197713
NZ_CP023992.1\|WP_099013486.1\|2774562_2775195_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224715
NZ_CP023992.1\|WP_099016890.1\|2770042_2771875_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP023992.1\|WP_099013479.1\|2757451_2759068_-\|regulator	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069869300.1\|2761898_2762579_+\|DUF4191-domain-containing-protein	gnl\|CDD\|379389	pfam13829, DUF4191, Domain of unknown function (DUF4191).	1.32889e-105
NZ_CP023992.1\|WP_069869288.1\|2776671_2778030_-\|MHS-family-MFS-transporter	gnl\|CDD\|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.59459e-163
NZ_CP023992.1\|WP_069869392.1\|2759281_2760097_+\|lipoyl(octanoyl)-transferase-LipB	gnl\|CDD\|184638	PRK14345, PRK14345, lipoyl(octanoyl) transferase LipB.	7.09059e-114
NZ_CP023992.1\|WP_069869294.1\|2771933_2772443_-\|inorganic-diphosphatase	gnl\|CDD\|376376	pfam00719, Pyrophosphatase, Inorganic pyrophosphatase.	1.78388e-79
NZ_CP023992.1\|WP_099013485.1\|2773350_2774406_+\|zinc-binding-dehydrogenase	gnl\|CDD\|176234	cd08273, MDR8, Medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family. This group is a member of the medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, but lacks the zinc-binding sites of the zinc-dependent alcohol dehydrogenases. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P)-binding Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	4.3328e-138
NZ_CP023992.1\|WP_099013487.1\|2775196_2775586_-\|cupin	gnl\|CDD\|380437	cd20303, cupin_ChrR_1, Marinobacter hydrocarbonoclasticus anti-ECFsigma factor ChrR, and similar proteins; 2 heterologous tandem repeats of cupin domain. This family contains bacterial anti-sigma factor such as ChrR from Marinobacter hydrocarbonoclasticus. Anti-sigma factor ChrR is a member of the ZAS (Zn2+ anti-sigma) subfamily of group IV anti-sigmas. It inhibits transcriptional activity by binding to the ECF sigma factor E (sigmaE), an essential factor to mount a transcriptional response to a singlet oxygen and for viability when carotenoids are limiting. This protein family likely contains two distinct homologous functional domains belonging to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	3.35845e-09
NZ_CP023992.1\|WP_079260419.1\|2769062_2769701_-\|LysE-family-translocator	gnl\|CDD\|224199	COG1280, RhtB, Putative threonine efflux protein [Amino acid transport and metabolism].	8.97895e-38
NZ_CP023992.1\|WP_069869298.1\|2763497_2764907_+\|type-I-glutamate--ammonia-ligase	gnl\|CDD\|273198	TIGR00653, Glutamine_synthetase, glutamine synthetase, type I. Alternate name: glutamate--ammonia ligase. This model represents the dodecameric form, which can be subdivided into 1-alpha and 1-beta forms. The phylogeny of the 1-alpha and 1-beta forms appears polyphyletic. E. coli, Synechocystis PCC6803, Aquifex aeolicus, and the crenarcheon Sulfolobus acidocaldarius have form 1-beta, while Bacillus subtilis, Thermotoga maritima, and various euryarchaea has form 1-alpha. The 1-beta dodecamer from the crenarcheon Sulfolobus acidocaldarius differs from that in E. coli in that it is not regulated by adenylylation. [Amino acid biosynthesis, Glutamate family].	0
NZ_CP023992.1\|WP_099013484.1\|2772526_2773231_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|379115	pfam13305, WHG, WHG domain. This presumed domain is around 80 amino acids in length. It is found to the C-terminus of a DNA-binding helix-turn-helix domain. This domain may be involved in binding to an as yet unknown ligand that allows a transcriptional regulation response to that molecule. The domain is named WHG after three conserved residues near the C-terminus of the domain.	1.75523e-11
NZ_CP023992.1\|WP_099013483.1\|2767460_2768678_-\|Ig-like-domain-repeat-protein	gnl\|CDD\|379864	pfam16640, Big_3_5, Bacterial Ig-like domain (group 3). This family consists of bacterial domains with an Ig-like fold.	1.09624e-09
NZ_CP023992.1\|WP_099013480.1\|2762775_2763243_-\|RDD-family-protein	gnl\|CDD\|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	1.40991e-10
NZ_CP023992.1\|WP_069869301.1\|2760403_2761354_+\|lipoyl-synthase	gnl\|CDD\|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	0
NZ_CP023992.1\|WP_069869297.1\|2765001_2765592_-\|Ig-like-domain-repeat-protein	gnl\|CDD\|379864	pfam16640, Big_3_5, Bacterial Ig-like domain (group 3). This family consists of bacterial domains with an Ig-like fold.	5.10747e-08
NZ_CP023992.1\|WP_099013477.1\|2754995_2756339_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|366721	pfam01593, Amino_oxidase, Flavin containing amine oxidoreductase. This family consists of various amine oxidases, including maze polyamine oxidase (PAO) and various flavin containing monoamine oxidases (MAO). The aligned region includes the flavin binding site of these enzymes. The family also contains phytoene dehydrogenases and related enzymes. In vertebrates MAO plays an important role regulating the intracellular levels of amines via there oxidation; these include various neurotransmitters, neurotoxins and trace amines. In lower eukaryotes such as aspergillus and in bacteria the main role of amine oxidases is to provide a source of ammonium. PAOs in plants, bacteria and protozoa oxidase spermidine and spermine to an aminobutyral, diaminopropane and hydrogen peroxide and are involved in the catabolism of polyamines. Other members of this family include tryptophan 2-monooxygenase, putrescine oxidase, corticosteroid binding proteins and antibacterial glycoproteins.	8.99008e-40
NZ_CP023992.1\|WP_099013478.1\|2756593_2757358_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|197713	smart00418, HTH_ARSR, helix_turn_helix, Arsenical Resistance Operon Repressor.	1.56152e-14
NZ_CP023992.1\|WP_099013486.1\|2774562_2775195_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	6.10235e-34
NZ_CP023992.1\|WP_099016890.1\|2770042_2771875_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.95479e-86
NZ_CP023992.1\|WP_069869289.1\|2775582_2776392_-\|carbon-nitrogen-hydrolase-family-protein	gnl\|CDD\|143605	cd07581, nitrilase_3, Uncharacterized subgroup of the nitrilase superfamily (putative class 13 nitrilases). The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13). Class 13 represents proteins that at the time were difficult to place in a distinct similarity group; this subgroup represents either a new class or one that was included previously in class 13. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	9.04294e-113

>NZ_CP023992.1|WP_069869297.1|2765001_2765592_-|Ig-like-domain-repeat-protein
MATPTITLVTVSPNPITVGQSVTLTATVIPLGPGTPTGDVTFVITGGPTVTGTLSGGTTSVTVPGLGVGAHAVLGNYNGDTNFSPSTGANVILVVQAATTTAVSSAPDPSTQGEPVTFTATVTPVAPGAGVPTGTVTFIIGAVGGGAFVQPLTAGTATLTLDTLGTGTAPVVAIYNGDTSFLPSSGTDTQTVNPAA
>NZ_CP023992.1|WP_069869298.1|2763497_2764907_+|type-I-glutamate--ammonia-ligase
MFQNADDARKFISDEDVKFVDVRFCDLPGVMQHFTVPAEAFDPNEELAFDGSSIRGFQAIHESDMALRADLSTARVDPFRRDKTLNINFFIHDPITGEQYSRDPRNIAKKAEAYLASTGIADTAYFGPEAEFYVFDSVRFDTKANESFYHIDSEAGAWNTGALQDNRGYKVRYKGGYFPVPPVDHFADLRAEISLELNRAGLQVERQHHEVGTAGQAEINYKFNTLLAAADDLMLFKYIVKNVAWKNGKTATFMPKPIFGDNGSGMHVHQSLWQGGSPLFYDEQGYAGLSDTARYYIGGILKHAPSLLAFTNPTVNSYHRLVPGFEAPVNLVYSQRNRSAAMRIPITGSNPKAKRVEFRAPDSSGNPYLAFSALLLAGLDGIKNKIEPAEPIDKDLYELAPEEHAGVPQVPTSLPAVLDSLEADHEFLLQGGVFTSDLIETWIDYKRTNEIAPLQLRPHPHEFELYFDV
>NZ_CP023992.1|WP_099013480.1|2762775_2763243_-|RDD-family-protein
MDKRQAIGSWLSGPRAAAEEMGVDFGYRGQGLGLPESGPGSIAPLGRRFGALFIDWGLCLLVSYALLSGRDAQAAGNWALLVFLGLSLVTVGTVGATPGKLLLRLRVIGEGGMRLSLPKAVLRSVLLVLVIPAVVWDRDTRGLHDRLSRAVQIRV
>NZ_CP023992.1|WP_069869300.1|2761898_2762579_+|DUF4191-domain-containing-protein
MARKETSENPGRLKQIALTYKMTKRVDPKVTLVVAGVGIVTFGVLLAIGFWIGHPIFLGILGFVLAFLAMAIIFGRRAERAAFGQMEGQPGAAAAVLENVGRGWSVTPAVAMNRNQDVIHRAVGKAGIVLVAEGNPNRVKSMLAAEKKKMARIVAEVPVHDVIVGSGEGQVEIKKLRTTLLKLPRVLPGAQVTVVNDRLRALGDLMSNMPIPKGPMPKGMRMPKGR
>NZ_CP023992.1|WP_020871972.1|2761690_2761888_+|hypothetical-protein
MPAAPVRPSVTDALLVLEGLLLRGGQRTARRNAWTAVLEDRRRAKDRDEAEHVLEAVSTGASQAT
>NZ_CP023992.1|WP_069869301.1|2760403_2761354_+|lipoyl-synthase
MSAVAPDGRKMLRLEVRNSQTPIERKPEWIKTRAKMGPEYTELHGLVKREGLHTVCQEAGCPNIYECWEDREATFLIGGDQCTRRCDFCQIDTGKPQALDRDEPRRVAESVRTMELKYATITGVARDDLEDGGAWLYAETVRQIHSLMPDTGVELLIPDFNAVPEQLAEVFSARPEVLAHNVETVPRIFKRIRPGFRYERSLEVITKAREAGLVTKSNLILGMGEERAEISQALQDLHDAGCELITITQYLRPSARHHPVERWVKPQEFVELKEEAEEIGYAGVMSGPLVRSSYRAGRLYQQAVERRNVAVASQAV
>NZ_CP023992.1|WP_069869392.1|2759281_2760097_+|lipoyl(octanoyl)-transferase-LipB
MTTASPGAAPGSSALRYVHLGFGADAVDYEEAWQEQRRVHAARFADEIPDTCLLLEHPPVYTAGRRTADNERPLDGTPVVDVDRGGKITWHGPGQLVGYPILKLPRPVDVIAHVRRLEEALLRTCAEFGLETTRVEGRSGVWVLGDPVEQRPALGGLKLDFDPRLADEEFDARLNGPEYAPSNAGQRREDRKLAAIGVRIAKGVTMHGFSLNCDPDNTWFDRIVPCGIRDAGVTSLSEELGRDVPIAEVLPVIERHLREVLESAVPLPRAV
>NZ_CP023992.1|WP_099013479.1|2757451_2759068_-|regulator
MTERPPQRIPNRQLAALIAEAGFSNAGLARRVDQLGLEHGLDLRYDKTSVTRWLRGQQPRGTTPALIAEVFTRRLGRRLTAQDLGLDACAPVYAGLEFAATPQEAVDIVSGLWRKDSGSHAELRKIAFTPAGLVVPSRDWLIGRPDDRVARGEPPAGPAPAGAAVGVGTGAGRLPAQGGRAGAQAAAAGAAGLAPGRGVMQGSQGPQSAHGGPGVHGGHGRAPLPRQRRHDRDRRGPGYRVTTGDIAALRSVGELFAALDQTYGGGHARQALVRYLEHEGEPMLRGSYNEATGRRLFGAIADLTRLAGWTSFDIAAHGLAQRYFVQALRLAQAAGDRTYGSYVLVTMSRQAVYLGHGREAVQLARVAQQGVGGGAPPVLQSLLHAIEARGHGVLGEVRACTASLARAERALEAARPGDEVPYWARLFDEAQLADEFGHCHRDLQQYRAAAQHAERSLQLHGAGCARSRLFCRVVLATARLGLGELEQACQLGAEAAHQASEMRSVRAVEYVRDFERRLEPYRDAAPVRGYRERVAALG
>NZ_CP023992.1|WP_099013478.1|2756593_2757358_+|helix-turn-helix-transcriptional-regulator
MATTTGARDADIARAAAAIADPSRARVLTALLEGRALPASVLATEAGVSASTVSGHLAKLLEAGVVRVERHGRHRYYRLTGPAVGEALEALARIAPPLPVTSLRQSSHAHALRRARTCYDHVAGALGVALLAALLERGVLEGGDGRFHPEAAESDRLSAPGNDTTYRLTEPGRAALAAFGVDADGLVAGRRPLIRYCVDWTEQRHHLAGALGAALTDRLFALDWIRRGGRRRVVHLTDAGRTGLERTFGVVLDN
>NZ_CP023992.1|WP_099013477.1|2754995_2756339_+|FAD-dependent-oxidoreductase
MLKRAHRTDVVIVGAGLAGLAAAHRLTGAGVAVTVLEAAPRVGGRMTTDTVDGFRLDRNGHLMNTSFPELRRTPGLGALALRPLAQGVLVHSEGRTHRVDTPRSMRGAFTTARALANAARAPLGSGLDQARLGAALGRLAALPADRLLARPDRPVSETLGGRGLPARTVEGVLRPLLVSLLSDPDLTTSSRCADLALRGYARGRLCLPAGGASTVPELLAAALPPGTVRTGVRAVSASTTAVATAEHGEFGCRAVLVATGAHDAAGLLPGLRVPAFHPVTVVHHTADRPPLREPALILAAGGRGPVAHTMVASEVDPSRTPPGRVLITSTVLGTPAALPTAELDRSVRAQLAAVYGTSTAGWQLLAAHHDPYAVPAMPAPHDPRRPVRLLSGLYVCGDHRDSSTVQGALASGRRAARAVLSDFGAPPDSGSGTTPDTGPDPFPAAAA
>NZ_CP023992.1|WP_099013483.1|2767460_2768678_-|Ig-like-domain-repeat-protein
MASPTVTLVTAAPNPAVAGQSVTLTATVIPLGAGTPTGTVTFVVGGGPTLTGTLSGGTTSVTVPNLTLGTHIVTATYNGDVNFTSSTGTTAVVVIQASTTTSVISAPDPSTLGQPVTFTATVTPVAPGAGVPTGSVTFIIGGSGGGTFVQPLSAGTATLSLSTLGVGTHTVVALYGGSADFLASSGTDTHTVNPGPAATTTTLASSVNPSVFGQPVTFTATVTPNLPTTGTPTGSVTFVISGTGGGTFTEPLSGGTATFITSGLGTGSHTVTATYSGDADFATSTSAPLTQTVDTANSITSLSSNPNPAEEGTPIDFVAFVAAMAPGDGTPTGTVAFTLVMGTTTVEMSVPVDAFGFAFLSDQILAAGTWDVSAVYSGDANFGASGVSDYTQVVTGAVSGVQAAI
>NZ_CP023992.1|WP_079260419.1|2769062_2769701_-|LysE-family-translocator
MVSIDRLLAFAAMSFLLIVIPGPSVLFVVGRALAQGRRAALTTVVGNTLGAYVLVVAVALGVGSVVERSAVVFTTLKLVGAAYLVHLGVKAVRQRRSLHAAFTGDGPAHGGLRTLWEGFAVGVANPKTIVFFAAVLPQFVDREQGHVAWQMLLLGLIFNAIAVISDSVWGLAAATARTWFARSPRRLAMVGGVGGLSMIGLGVTVAATGRAD
>NZ_CP023992.1|WP_099016890.1|2770042_2771875_+|ABC-transporter-ATP-binding-protein
MTAWERNPVTTRAMARRLPQLVRRSLALAWKVDRKAVVALLVCQALSGFFEAFGLLATTGTITALISSGQITDRLREALPSIAVLAGAAGLRALLGIAVGNISSRLSPRISREAETQMLDAAINAELAAYDNPGFNDKWDAADRGAEVARDLITESQQLMACLSSLIAAAGVVTVLHPALLPLLLLAALPQGIAGMKAARVQYETSRAMSADRRTLGLLRWYMMDKDIADQLRSGTMAEFLLKRYRAIGARVDAATDKAVHRGARYAVLGAVAGGVASGLVWVSLALLLGAGRMSVASAGTAVFALRTVGASLQGMVGYGTRLFRTGLYLDDWAEFIEEAGGHRMVRGTRVPAPPRVIRTEGLTYAYPESDAPALDDVTLEVRQGEVLALVGENGSGKTTLSKLLTGLYLPTKGAVTWDGVGVEELDPQAMWRHTAVVPQDYAHWPLSARDNITLGQPHGGDERVREAAVRSGAHEVVDGLRSGLDTLLARQWWGGVELSGGQWQRIALARAFHRPAGLLVMDEPTSALDARAEHRIFAGLRRMAEDRAVVLVTHRLANVAVADRIVVLERGRVIQQGTFAELTGSPGLFRELWELQNDRGVPAPRGETP
>NZ_CP023992.1|WP_069869294.1|2771933_2772443_-|inorganic-diphosphatase
MEHGEFDVVVEIPEGSRNKYEMDHETGRIRLDRMLFTSTKYPADYGYVDHTLGRDGDPLDALVTVAEPTFPGCVILCRAIGMYCMRDEQGPDEKILCVPAHDPRYVGVQDIEDVPEFDRKEITHFFEVYKDLEPGKSVEGSHWEGRDRAYAEIAASRARAAETGRFQSP
>NZ_CP023992.1|WP_099013484.1|2772526_2773231_-|TetR/AcrR-family-transcriptional-regulator
MATARRERYRKQTREEAKAVALAQLSESGTAGISVNAIAKAMGMTGPALYRYFASRDELLTELITDTYRDLAETLARAVADAAPADRFRALARALRDWAKRQPDRYLLIYGTPVPGYHAPPETTEIAAGLMRTIFDACATVGEAGEAGGGGVGADGSRQQPLTELEAELARHLEGTGPWGPGEEPGGEMKGRALRTWTRLHGVISLDVQGQFTGMGFDPSVLFEAEIDALVRGG
>NZ_CP023992.1|WP_099013485.1|2773350_2774406_+|zinc-binding-dehydrogenase
MITEVVLPGQVEPEGLELRTRPLPEPGAGQALVAVEASGVSFAEQQMRRGKYYDQPPFPFVPGYDLVGTVVSTGPGVDPALRGRRFAALTKIGGWASHTLVDAGDLVEVPEGVDAAEAETVVVNGITAWQMLHRVAKVRPGMTVLVHGANGGVGTTLVQLARHAGIKVIGTASPRHHDAVRALGATPLDYRDPDLPGRVRALAPGGVDAVFDHVGGEGIVDSFRLLARGGTLVSYGTAATRDVPGSSRAPVLKLFARLFLWNLLPNGRGAHFFNLWAGRRRKAAYQARIRADLGQVLALLASGDFTAMVAARIPLSDAAEAMRLAESGTVTGKVVLVADQDARQGGEEGAR
>NZ_CP023992.1|WP_099013486.1|2774562_2775195_+|GntR-family-transcriptional-regulator
MPAQSGREKAYAFLKETVLTDPDMQGSFLTEQEIADRIGISRTPIREALLLLAAEDLVQLVPKRGAHIAPLSGREITELMELRGIVERYAAEHAIETGTVPVGKLTELLERQRELMGPEQAKEFIAIDHLFHATMIAAVGNELLNRHYEGLRSRQIRAGVVALYNQTGRQKEVLGEHRAILEAVAAGDTEAARTAISAHLESTLKVLLAG
>NZ_CP023992.1|WP_099013487.1|2775196_2775586_-|cupin
MSGTGGAKPEREFHLPSGPWRRPPGAAAGVSEQILAVDGSGTHTTALVCWEPGTDTSSSGVARHDGWEEVYLLEGSMRDLTLGETFSRGFYACRPPGMPHGPWVSEEGVTMLVITYPEAVPVPGGGAGR
>NZ_CP023992.1|WP_069869289.1|2775582_2776392_-|carbon-nitrogen-hydrolase-family-protein
MPLRIALSQITTGPDPASNLALLRRETQRAAEAGARLVAFPEAAMACFGTRLGPIAEPLDGPWATEVRQIAKDAGLVVVAGMFTPAPDGRVTNTLLATGPGVETSYDKIHLYDAFGFAESKTVAPGSEVVTFDLDGVRIGLATCYDVRFPELFRAHADAGAVLSLLPASWGAGPGKREQWELLTRARALDATVWLAAVGQADPAASGLTAATSAPTGIGHSALIGPDGTVRERLDAGPGLLVGEVDTEEVTAVRRTVSVLANRRLGVQP
>NZ_CP023992.1|WP_069869288.1|2776671_2778030_-|MHS-family-MFS-transporter
MQPTASSAPQPRADRSGVRRAFVASLTGTALEWYDFAVYSAAAALVFGDLFFPSKDPFTGTLLAFSTYAVGYLSRPLGGFVFGRLGDVIGRKKVLIATLVLIGGATLLIGLLPTYATVGVAAPAALVLLRFAQGVGVGGEWGGAVLLSSEFGDPRRRGFYASAAQVGPPAGNLLANGVLAALGAALTEDQFLSWGWRVAFLLSGALVAFGLWVRAKLEETPVFKAMEAAQDRPEAPLREVFTTQPKALTAAILSRVAPDVLYAMFTVFVLTYATEELDMSRGSALTAVLIGSSLQIVLIPLAGALSDRVNRRLLYGGAAVAAGVWPFLFFPLVADGSWALLTLGVVGALVIHSLMYGPQAAFVAEQFSPRLRYTGSSLAYTLAGLIGGAIAPLLFTALLGTYHAWVPLAIYIAITAVVTVIGLWLGRDPGSAEDEEPLPLPVGQTASSTTVS

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Crispr_ID: NZ_CP023992_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_4

2825091-2825176

Orphan

Consensus_repeat	Method
CCAACATGCGGCTCCCCCGCACGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_4

>merge|NZ_CP023992|4|2825091-2825176|CRISPRCasFinder
CCAACATGCGGCTCCCCCGCACGGACGCGACCCAAGGCACCCCGAAGCGGCGCAAGGCTGACCCAACATGCGGCTCCCCCGCGCGG

>NZ_CP023992|4|4|2825091-2825176|CRISPRCasFinder
CCAACATGCGGCTCCCCCGCACGG	ACGCGACCCAAGGCACCCCGAAGCGGCGCAAGGCTGAC
CCAACATGCGGCTCCCCCGCGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069869257.1\|2833623_2834448_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|366444
NZ_CP023992.1\|WP_069869265.1\|2818743_2820105_-\|glutamine-synthetase	unknown	unknown	gnl\|CDD\|223252
NZ_CP023992.1\|WP_069869258.1\|2831518_2832379_+\|3-methyl-2-oxobutanoate-hydroxymethyltransferase	unknown	unknown	gnl\|CDD\|234723
NZ_CP023992.1\|WP_099013501.1\|2809510_2810170_+\|DNA-binding-protein	unknown	unknown	gnl\|CDD\|225512
NZ_CP023992.1\|WP_069869260.1\|2829033_2829642_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379883
NZ_CP023992.1\|WP_099013502.1\|2810187_2811114_+\|hydroxyurea-phosphotransferase	unknown	unknown	gnl\|CDD\|309685
NZ_CP023992.1\|WP_079257357.1\|2827828_2828857_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|197318
NZ_CP023992.1\|WP_099013507.1\|2824110_2824896_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|131480
NZ_CP023992.1\|WP_099013500.1\|2808371_2809514_+\|threonine-synthase	unknown	unknown	gnl\|CDD\|107206
NZ_CP023992.1\|WP_099013504.1\|2815323_2818572_-\|bifunctional-[glutamine-synthetase]-adenylyltransferase/[glutamine-synthetase]-adenylyl-L-tyrosine-phosphorylase	unknown	unknown	gnl\|CDD\|237613
NZ_CP023992.1\|WP_099013509.1\|2834520_2838063_-\|AfsR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|226418
NZ_CP023992.1\|WP_079257359.1\|2832613_2833627_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|130256
NZ_CP023992.1\|WP_099013503.1\|2812970_2814071_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_079257362.1\|2838785_2839583_+\|site-2-protease-family-protein	unknown	unknown	gnl\|CDD\|100079
NZ_CP023992.1\|WP_099013505.1\|2820535_2822197_+\|multicopper-oxidase-family-protein	unknown	unknown	gnl\|CDD\|259938
NZ_CP023992.1\|WP_079257358.1\|2829638_2831261_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|184957
NZ_CP023992.1\|WP_087684407.1\|2812566_2812887_+\|nitroreductase-family-deazaflavin-dependent-oxidoreductase	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013510.1\|2838087_2838633_-\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|99749
NZ_CP023992.1\|WP_099013506.1\|2822329_2824084_+\|NAD+-synthase	unknown	unknown	gnl\|CDD\|237577
NZ_CP023992.1\|WP_099013508.1\|2826405_2827620_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|225371

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069869265.1\|2818743_2820105_-\|glutamine-synthetase	gnl\|CDD\|223252	COG0174, GlnA, Glutamine synthetase [Amino acid transport and metabolism].	0
NZ_CP023992.1\|WP_069869258.1\|2831518_2832379_+\|3-methyl-2-oxobutanoate-hydroxymethyltransferase	gnl\|CDD\|234723	PRK00311, panB, 3-methyl-2-oxobutanoate hydroxymethyltransferase; Reviewed.	2.81204e-165
NZ_CP023992.1\|WP_099013501.1\|2809510_2810170_+\|DNA-binding-protein	gnl\|CDD\|225512	COG2964, COG2964, Uncharacterized protein conserved in bacteria [Function unknown].	1.44905e-56
NZ_CP023992.1\|WP_069869260.1\|2829033_2829642_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	3.398e-19
NZ_CP023992.1\|WP_099013502.1\|2810187_2811114_+\|hydroxyurea-phosphotransferase	gnl\|CDD\|309685	pfam04655, APH_6_hur, Aminoglycoside/hydroxyurea antibiotic resistance kinase. The aminoglycoside phosphotransferases achieve inactivation of their antibiotic substrates by phosphorylation utilising ATP. Likewise hydroxyurea is inactivated by phosphorylation of the hydroxy group in the hydroxylamine moiety.	3.63753e-62
NZ_CP023992.1\|WP_079257357.1\|2827828_2828857_-\|hypothetical-protein	gnl\|CDD\|197318	cd09084, EEP-2, Exonuclease-Endonuclease-Phosphatase (EEP) domain superfamily; uncharacterized family 2. This family of uncharacterized proteins belongs to a superfamily that includes the catalytic domain (exonuclease/endonuclease/phosphatase, EEP, domain) of a diverse set of proteins including the ExoIII family of apurinic/apyrimidinic (AP) endonucleases, inositol polyphosphate 5-phosphatases (INPP5), neutral sphingomyelinases (nSMases), deadenylases (such as the vertebrate circadian-clock regulated nocturnin), bacterial cytolethal distending toxin B (CdtB), deoxyribonuclease 1 (DNase1), the endonuclease domain of the non-LTR retrotransposon LINE-1, and related domains. These diverse enzymes share a common catalytic mechanism of cleaving phosphodiester bonds; their substrates range from nucleic acids to phospholipids and perhaps, proteins.	1.17215e-21
NZ_CP023992.1\|WP_099013507.1\|2824110_2824896_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	5.96394e-27
NZ_CP023992.1\|WP_099013500.1\|2808371_2809514_+\|threonine-synthase	gnl\|CDD\|107206	cd01563, Thr-synth_1, Threonine synthase is a pyridoxal phosphate (PLP) dependent enzyme that catalyses the last reaction in the synthesis of threonine from aspartate. It proceeds by converting O-phospho-L-homoserine (OPH) into threonine and inorganic phosphate. In plants, OPH is an intermediate between the methionine and threonine/isoleucine pathways. Thus threonine synthase competes for OPH with cystathionine-gamma-synthase, the first enzyme in the methionine pathway. These enzymes are in general dimers. Members of this CD, Thr-synth_1, are widely distributed in bacteria, archaea and higher plants.	6.14583e-115
NZ_CP023992.1\|WP_099013504.1\|2815323_2818572_-\|bifunctional-[glutamine-synthetase]-adenylyltransferase/[glutamine-synthetase]-adenylyl-L-tyrosine-phosphorylase	gnl\|CDD\|237613	PRK14109, PRK14109, bifunctional [glutamine synthetase] adenylyltransferase/[glutamine synthetase]-adenylyl-L-tyrosine phosphorylase.	0
NZ_CP023992.1\|WP_099013509.1\|2834520_2838063_-\|AfsR-family-transcriptional-regulator	gnl\|CDD\|226418	COG3903, COG3903, Predicted ATPase [General function prediction only].	1.59398e-57
NZ_CP023992.1\|WP_079257359.1\|2832613_2833627_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|130256	TIGR01188, drrA, daunorubicin resistance ABC transporter ATP-binding subunit. This model describes daunorubicin resistance ABC transporter, ATP binding subunit in bacteria and archaea. This model is restricted in its scope to preferentially recognize the ATP binding subunit associated with effux of the drug, daunorubicin. This transport system belong to the larger ATP-Binding Cassette (ABC) transporter superfamily. The characteristic feature of these transporter is the obligatory coupling of ATP hydrolysis to substrate translocation. The minimal configuration of bacterial ABC transport system: an ATPase or ATP binding subunit; An integral membrane protein; a hydrophilic polypetpide, which likely functions as substrate binding protein. In eukaryotes proteins of similar function include p-gyco proteins, multidrug resistance protein etc. [Transport and binding proteins, Other].	2.34174e-130
NZ_CP023992.1\|WP_069869257.1\|2833623_2834448_+\|ABC-transporter-permease	gnl\|CDD\|366444	pfam01061, ABC2_membrane, ABC-2 type transporter.	3.13342e-18
NZ_CP023992.1\|WP_079257362.1\|2838785_2839583_+\|site-2-protease-family-protein	gnl\|CDD\|100079	cd06158, S2P-M50_like_1, Uncharacterized homologs of Site-2 protease (S2P), zinc metalloproteases (MEROPS family M50) which cleave transmembrane domains of substrate proteins, regulating intramembrane proteolysis (RIP) of diverse signal transduction mechanisms. Members of the S2P/M50 family of RIP proteases use proteolytic activity within the membrane to transfer information across membranes to integrate gene expression with physiologic stresses occurring in another cellular compartment. In eukaryotic cells they regulate such processes as sterol and lipid metabolism, and endoplasmic reticulum stress responses. In prokaryotes they regulate such processes as sporulation, cell division, stress response, and cell differentiation. This group includes bacterial, eukaryotic, and Archaeal S2P/M50s homologs with a minimal core protein and no PDZ domains.	2.95396e-43
NZ_CP023992.1\|WP_079257358.1\|2829638_2831261_-\|MFS-transporter	gnl\|CDD\|184957	PRK14995, PRK14995, SmvA family efflux MFS transporter.	1.02907e-79
NZ_CP023992.1\|WP_099013505.1\|2820535_2822197_+\|multicopper-oxidase-family-protein	gnl\|CDD\|259938	cd13870, CuRO_2_CopA_like_1, The second cupredoxin domain of CopA copper resistance protein like family. The members of this family are copper resistance protein (CopA) homologs. CopA is multicopper oxidase (MCO) related to laccase and L-ascorbate oxidase, both copper-containing enzymes. CopA is involved in copper resistance in bacteria. CopA mutant causes a loss of function, including copper tolerance and oxidase activity, and copA transcription is inducible in the presence of copper. Although MCOs have diverse functions, majority of them have three cupredoxin domain repeats that include one mononuclear and one trinuclear copper center. The copper ions are bound in several sites: Type 1, Type 2, and/or Type 3. The ensemble of types 2 and 3 copper is called a trinuclear cluster. MCOs oxidize their substrate by accepting electrons at a mononuclear copper center and transferring them to the active site trinuclear copper center. The cupredoxin domain 2 of 3-domain MCOs has lost the ability to bind copper.	3.01827e-57
NZ_CP023992.1\|WP_099013510.1\|2838087_2838633_-\|Uma2-family-endonuclease	gnl\|CDD\|99749	cd06260, DUF820, Domain of unknown function (DUF820). This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. They have been predicted to belong to the PD-(D/E)xK superfamily of nucleases.	4.87563e-17
NZ_CP023992.1\|WP_099013506.1\|2822329_2824084_+\|NAD+-synthase	gnl\|CDD\|237577	PRK13981, PRK13981, NAD synthetase; Provisional.	0
NZ_CP023992.1\|WP_099013508.1\|2826405_2827620_-\|MFS-transporter	gnl\|CDD\|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	9.8365e-92

>NZ_CP023992.1|WP_099013507.1|2824110_2824896_-|alpha/beta-fold-hydrolase
MTSTSTSPLARVVRGSGPGLLLAHGGTGSIEGNYGPILDGLAERRRVVGPDYPGSGRTPRANGPLDLDTLADQLVATAVEEGLETFAIAGYSLGGPVALCAATRHPERVTALVLTATFAHPSARMRLLVEDWLRLLRSGDREAAARWTTLVAAGAPYLDRMTPEELATLIAYARDSVPPGAVDQVELVDRVDVREDLGRIRVPTLVISTALDTMATPYHHRQVADGIPGARFAELASGHLPFAEAPGEWLGLIRAFLDAQA
>NZ_CP023992.1|WP_099013506.1|2822329_2824084_+|NAD+-synthase
MPQLRLALNQIDSTVGDLDGNTESILHWTRHSAEQGAHLVAFPEMVLTGYPVEDLALRSSFVEASRAALRSLAERLDAEGLGEVPVVVGYLDRSEGARRYGQPAGSPQNAGAVLHRGAIALTFAKHHLPNYGVFDEFRYFVPGDTLPMVRVHGVDVALAICEDLWQDGGRVPASRSAGAGLLLSINASPYEREKDDTRLDLVRKRAQEAGCTTAYLAMIGGQDELVFDGDSIVVDRAGEVIARAPQFAEGCVLLDLELPAADPDSVPEGVVDDGLRIDHVTLSANPLPGYEPELAGGEAERLGDDEEIYTALVVGLRAYVAKNGFRSVLIGLSGGIDSSLVAAIACDAVGAQNVYGVAMPSRYSSEHSIADATELARRTELNFRTVSIAPMFDAYMGSLGLTGLAEENLQSRLRGTMLMAISNQEGHIVLAPGNKSELACGYSTLYGDSVGAYGPIKDVYKTSIFRLSKWRNRAAQERGQTPPIPENSISKPPSAELRPGQVDTDSLPDYDILDRILELYVDRDQGRAEIVAAGYDDALVTRILRLVDTAEYKRRQYPPGTKISAKGFGKDRRLPITNRWREHD
>NZ_CP023992.1|WP_099013505.1|2820535_2822197_+|multicopper-oxidase-family-protein
MHEKTRRAVLGTGIAAAGSGLLTACGSPGPRPHAGGHGGLDGDATGAPARAGAPADDVPAEYVSPHGPEVAAVEQRRGPGPVREFRLTATATTLDIGARKVASWAYEDQVPGREIRVTAGDTIALTLANNLPQSTTLHWHGIRLRNDMDGVPGVTQRAIKTGAAFDYRFTAFYPGTYWIHPHSGVQLDRGLYAPLIVEDPKEPLTYDKEWVVVLDDWLDGVGGRTPDKVFERLSGGKSGHSMEGMAGGGKPGAKAEGGAKSTAKGTAKGGAKGTGVRATARRKAAPSESGPLGGHAGDVTYPYYLVNGRSPESPQVFRAKRGDRVRIRIINAGGDTAFRVALGGHRMTVTHTDGYPVVPARTDALLLGMGERYDVLVTVKDGVFPLAVIAEGKGRSAMAVLRTRGKNPVKFPRPKELDGELLTADRLKAAEEVRLTPKEPDRIIRMRLTGSMRRWDWAINDRPYDPSQRYPVRAGERVRISFINGTDMWHPVHLHGHTFALPDDGPRKDTTILLPHHKVNVDLDADNPGLWMVHCHNVYHSESGMMTILGYQK
>NZ_CP023992.1|WP_069869265.1|2818743_2820105_-|glutamine-synthetase
MDKQQEFVLRTLEERDIRFVRLWFTDVLGFLKSVAVAPAELEGAFDEGIGFDGSAIEGFARVYESDMIAKPDPGTFQILPWRAEAPGTARMFCDILMPDGSPSFADPRFVLKRILAKTSDLGFTFYTHPEIEFFLLNQKPVDGTRPVPADSSGYFDHTPQNIGMDFRRQAITMLESMGISVEFSHHEGAPGQQEIDLRYADALSTADNIMTFRLVMKQVALEQGVQATFMPKPFSEFPGSGMHTHLSLFEGDRNAFYESGAEFQLSKVGRSFIAGLLRHAGEISAVTNQWVNSYKRIWGGSKRTAGAGGEAPSYICWGHNNRSALVRVPLYKPGKTGSTRVEVRSLDSGANPYLAYAVLLAAGLKGIEGGYELPAGADDDVWALSDAERRSLGIEPLPQNLGEAIDLMERSELVAETLGEHVFDFFLRNKKQEWEEYRSEVTPFELRKNLPVL
>NZ_CP023992.1|WP_099013504.1|2815323_2818572_-|bifunctional-[glutamine-synthetase]-adenylyltransferase/[glutamine-synthetase]-adenylyl-L-tyrosine-phosphorylase
MSVPQGRRSSNVTRLLRHGFTDASAAQRLLDAPELAAVRSDPVLLEALGATADPDLALLGLLRLVEALPEEEAKEAGAGEDGGQRAGSRQALLDTLVTAKPLRDRLLGVLGASEALGDHLARHPGDWHALVTYESADLHPATPEFERALAEGVWGEPGAGVPRPDALRVAYRRALLAIAARDVCGTTDLTQTAAELADLATATLRAALEIAVEEQPQDAAACRLAVIGMGKCGGRELNYVSDVDVIFVAESVEGVDEDEAVRAATRLASRLMRVCSDVTVEGTIWPVDANLRPEGRNGPLVRTLSSHLAYYQRWAKTWEFQALLKARPVAGDEALGQAYVDALAPMVWQAVERENFIPDVQQMRRRVVENIPVSEVDRELKLGPGGLRDVEFAVQLLQLVHGRSDESLRSGTTLDALAALAAGGYVGRTDAAALDAAYRFLRTMEHRLQLYRLRRTHLMPEGEADQRRLGRSLGFRTEPVTELGTAWRRHAREVRRLHEKLFYRPLLDAVAQLQPGEIRLSPEAAGQRLTALGYADPAGALRHLEALASGVTRKAAIQRTLLPVLLGWFADSAEPDAGLLGFRKVSDALGKTPWYLRLLRDEGAAAENLARVLSAGRLAPDLLLRAPEAVALLGDPEGLRPRGRAHLEQEVLAAVGRADGAEQAVAAARGVRRREMFRTAAADIIESARLANGEVRPTVSWPPAGDQPPGGRTPGRATGAAPAASATRAPEVPSALRASEPHVPARPAPPAAEPPVDAATLIDMVGGALSDLNAATLAGALRAAVRDTWGDELPTRFAVIGLGRFGGHELSYGSDADVLFVHEPREGADDQEAARAAFAVANEMRRLLQLPSVDPPLLIDADLRPEGKSGPLVRSLASYAAYYRRWALVWESQALLRAEPVAGDPGLGERFIELIDPLRYPSEGLGEDAIREIRRLKARMESERLPRGADPTTHAKLGRGGLSDVEWTVQLIQMRHGWAEPGLRTTRTREALAAAHAAGLIATEDAQTLDEAWVLASRVRNAVMLVRGRPGDTFPTDVRELAAVGRYLGYGPGHVGELLEDYRRTTRRARAVVERLFYDYEG
>NZ_CP023992.1|WP_099013503.1|2812970_2814071_+|hypothetical-protein
MKQLLGGARRRTALVGGAVVVLVAAGLGTWATDTWPFDGKDTYCWGAWKEDSGPGFLSRKALDEDNASRTSKETAPTPRRQRGQCTVSLHSERVGSDGDQIVAETKITVTYGPAPEGAGQRLEWIDGYLGDRAMPLPDGLPGATDGKQALLVLPEGCDTRDGRPTAVTLDTLARTVYSDTTMSADAGLGGSQSVARLLVAVANRAMEKAGCAPAEPLEAVSPMTTLPEEDESFFTRACRIRGLEFGKEGRDLEYQVGAVTRDFQSCSVRTQRGDGRYFDALMVAQPRFSALLDGVTGTKAPARGWRGTGVFADDYKVVRADCAGRPLTVLMLAPSLHETTPYFTAFANAVARRVGCAPIAPGGSSR
>NZ_CP023992.1|WP_087684407.1|2812566_2812887_+|nitroreductase-family-deazaflavin-dependent-oxidoreductase
MVGLRSSPRWGRRVSGRLTVVTYTGRRSGRTFSTPVAYRRAADAVTITVAMPERKLWWRNFTGEGGPISLDLDGSDRTGHAVARVDEKGRVTITVRLDQPPAPNSP
>NZ_CP023992.1|WP_099013502.1|2810187_2811114_+|hydroxyurea-phosphotransferase
MTPPIRDIDIPEAFAASFGERDATDRAWLAALPRLAADFLDRWDLRPAGPAAHGMASLVLPVTGADGTPAALKLQQVKEETEGVPLGLRTWNGDGVVILLDHDPDTGTMLLERLDASRPLSSLPDDTAALGVLADLLARLTSVPAPDGLRRLSDIAAAMLERTPGAVPALRDPAERRLVRVCASAVAELLDEPGDRLLHWDLHYDNILAGEREPWLAIDPEPLTGDPGFELLPALDNRWDEVLAAGDPTRAVLRRFDLLTEALGLDRRRATGWTLGRVLENALWDIEDGKTALEPAQVTIATALLNHR
>NZ_CP023992.1|WP_099013501.1|2809510_2810170_+|DNA-binding-protein
MTGARRQETAGSPEDELLLREAEKIVVALGRMFPGLCEVVLHDLRNPDQSIRAIESNLSGREVGEPATELGLARIQDPGFPDIVQNYANRFPDGRPAKSTSVGIKNSAGQYVAAICLNLDVSLFASAARSLNNLVRTDEQEQPLTETLRARTAAELRAVIEEFAAARGQTPRSLGTPAKKELVRTLKTSGFLQVKHSVQVVTELLGVSRATVYNYLRSP
>NZ_CP023992.1|WP_099013500.1|2808371_2809514_+|threonine-synthase
MRAEPRSEAHYVDERSGATYPIDDPRWCGDDGAPLTVSALPGITREQVDTGARSLWRYRAALPVPIDAPVSLGEGCTPLVEKSWGEDRVRFKLEWFSPTGSFKDRGTSVMISLLAQRGVREVIEDSSGNGGASVSAYCAAAGIRARILAPATTSPAKILQSRAYGAEVQLVPGDRDATAAEALRQSAHTYYASHNWHPFFLQGTKTLAYELWEDLGFTAPDAVVTVAGAGSTVLGCDLGFSELLGAGQITRRPRLLVAQPAHCAPLHAAFHAGTETPVPFDHAPTIAEGTAIREPVRFPEVLRAIRRSEGDMAAIPEDAIASAVRRLAAMGLYAEPTSATAAAAIEVFRARGAIRPGETTVVLLTGSGLKATPTMTELFG
>NZ_CP023992.1|WP_099013508.1|2826405_2827620_-|MFS-transporter
MPLALLALAVSAFGIGTTEFVMMGLLPNVAHDLDTSVPTAGYLVSAYAIGVVVGAPLLTALGSRIPRKRMLVLLMALFTVGNLASAFAPSFGLLIAGRVLAGLPHGAFFGVGAVVAARLVSEDRRARAVATMFLGLTIANIVGVPVATLLGQNLGWRATFLVVSAIGVVAMAALARLVPRVSLEQHGGLRQELGALRDRQVLLGLLTAVFGFAGVFAVYSYLASMMTEVTGFGESTVTLVLALFGIGMTLGALVAGPLTDRALRPTLYGSLAALAVVLVLFDFTVHVKWAALVSVVVLGAVGFMTTTPLQMLVMNKAQHAPTLASASNHSAFNLANAGGAWLGGAAIAAGWGWTSPTLVGAVLAVIGLAIALIAGVNDRAPVGGSRVVASGASGEGVRRLSEVG
>NZ_CP023992.1|WP_079257357.1|2827828_2828857_-|hypothetical-protein
MTQAYTQEPGQLGDAPRRSDSRIGRLLDRLRDDRGIWRRGLVLAAIAILLALVMIFHADIPNRVGNLGSLLETFLPWLGLFLPVLLVLAVVRRSASAVLALVLPVAVWLNLFGGLMFFDKSGSGGGELTVVTHNVNAENGDPTGTAKDVAASGADVVALEELTSAAVPTYERALAGTYRYHTVQGTVGLWSKYPLSGTKPVDIKLGWTRALRTAVATPRGEVGVYVAHLPSVRVKFNAGFTAGQRDASAEALGQAIAREPLRKVILLGDLNGTMNDRALAPVTSQMRSAQGAAGDGFGFSWPASFPMARIDQIMVRGVDPVSAWALPRTGSDHLPLAASVDY
>NZ_CP023992.1|WP_069869260.1|2829033_2829642_-|TetR/AcrR-family-transcriptional-regulator
MTAPESSAPRLRGRPRSPATDAAIIEAALRLLEEGASLGGLSIEGIAREAGVGKATVYRRWPGKEALMLDVLRSLEEPSPEPAGVSVRDDLVTILEFMRRRGLAKRNSALLRSVITQMHAHKELWRAYDENVIAARRACLRAVLRRGRESGEIRADVDLELLADLFTGPMLTRAMLHEWRELPDGLAERIVDTVLEGVSPRR
>NZ_CP023992.1|WP_079257358.1|2829638_2831261_-|MFS-transporter
MATSTTQGAPDGSGVPAEIHRRRWAILVVLMFSVLVVVLDNSILNVAMKTIASPKPTGLGATQSQLEWAINSYTLVFAGLLFTAGILGDRIGRKKVLLGGMAVFGMGSVLAAFSGSPGELIGFRALMGLGAAFVMPATLAILVNVFEREEQAKAIGIWVAAVGLAIAIGPITGGLLLEHFWWGSVFFVNVPVVIVGLIAMVMLVPDSRDPAPGRVDPLGVLLSVVGLVLLVYGIIKGGQLADFTDAQVLASIGGGLAVLALFVLHEKRSDHPAIDVGYFRNPAFSAAIAAVALVFFALMGVTFFMVFYTQSVRGYSALQSGLLILPLAVAQLIFAPRARLVVERFGARAVCTCGMLLVAATMSGFLLLGVDTPIIVLEVLFFCQGAGMAHIMPPVTTAIMQALPRQKAGSGSALNNTFRQVGGALGVAVLGSVLSAAYRDGIRDTLAAVPGLPDSVRRSAGESVEATLGVAEKLGPKGQALVGPAQDAFVHAMHITALGSAGVALLGALVVLAFLPGKGASGQAPDDGRPRSREEASAHR
>NZ_CP023992.1|WP_069869258.1|2831518_2832379_+|3-methyl-2-oxobutanoate-hydroxymethyltransferase
MTHVNPAQKQSEKALYGGTGSRRITVRDIAAAKGRAEKWPMLTAYDAMTASVFDQAGIPVLLVGDSMGNCHLGYESTVPVTMDEIALLSAAVVRGTRRALVVGDLPFGSYQEGPVQALRNATRLVKEAGVGAVKLEGGERSAHQIELLVQSGIPVMAHVGLTPQSVNAYGGYPVQGRGEEAAQQLLRDAKAVQDAGAFAVVLELVPAELAAEVTRSLHIPTIGIGAGPDCDGQVLVWTDMAGMTDGRVPRFVKQYAQLRQSLGDAARAFAEDVVGGAYPAEEHSFH
>NZ_CP023992.1|WP_079257359.1|2832613_2833627_+|ATP-binding-cassette-domain-containing-protein
MTRREHRIRDGNAVEVRGLVKHFGDTKAVDGVDLDVPEGTVLGVLGPNGAGKTTLVRCLSTLLVPDAGTAVVAGYDVVRQPRQLRRTIGLTGQYASVDEKLPGWENLYMIGRLLDLSRREARARADAMLERFSLTEAGKRRVRTYSGGMRRRLDLAASMIGRPSVLYLDEPTTGLDPHSRNEVWNEVRRMVADGATVLLTTQYMEEAEQLANHLTVIDRGRVIADGRVNELKAKIGGRTLQIRPSDPGELHRMVGAITQAGLEGIGGATADVEGGLVNVPIASDEQLTALIGLLGQRGFAIAGIDTHLPSLDEVFLAITGRMSSTPQDYKTLEEVPA
>NZ_CP023992.1|WP_069869257.1|2833623_2834448_+|ABC-transporter-permease
MSTATMTAPMRGKSDGRIGPRANLRHIGALVRRNAMQIRYEPFAMFDALAMPIVFALLFTYVFGGAMTGGNRSEYVNYFIPGLMAMGGLNIAMSIGIGVNDDFSKGVMDRFRTMPIARSSVLIAKLIVESGRMLVSTLILLIMGFTMGFELETGPVELLAAVALSVLFGSSLTWIFMLLGMSMPTPQAVSGMGFLVMMPLQFGSSIFAPTATMPDWLRAFTEYNPLSRLADAARALTSGHGAVAEPVMVTLGWAVALTVVVAPLAVRRFRNKTS
>NZ_CP023992.1|WP_099013509.1|2834520_2838063_-|AfsR-family-transcriptional-regulator
MHQNGSVRYGILGTTQARHDDGTPVAIGGARLRALLTALALAAGRARTTGVLIGEIWDTDPPADEQGALQALVGRLRRVLGKDAVESVPGGYRLSADPDDIDLHRFERLADEGTRALADGDPAKAVDLLDAALGLWRGPALSDLPDATAPAARAEARRLEARRARLAADLALGRAGQALPALTGLCDAHPLDEPLHALRIRALRDVGRAAEALAAYEEIRTEIAERLGVDPGPELRALHAELLRASGEGFPAVRPGSAAAGSVSSGSAPSGPVSSGPVPSGPVPSGPAPSGLASSGPVPSGLASSGPVPSGPVPSGPASPGPVPGRAGGGNLRARLTSFVGREGDLVTLRGDLAGHRLITLLGPGGAGKTRLSQEAAEAAAAAWPDGVWLAELAPVDDPETVPETVLSAVGGRETVILGTAAEGLRAAADPTVRDPRARLIEHCAPRRMLIVLDNCEHLVESAAHLAESLLAHCPGVTILATSREPLAVPGELVRPVEPLPDPVALRLLQDRGAAARPGFRTEDDPAACAEICRRLDGLPLAIELAAARLRLLTPRQLADRLDDRFRLLTSGSRTALPRQQTLRAVVDWSWGLLDAAERTVLARLSVFAGGCGLAEAEAVCGGAEGRPGGVEPRDVAVLLGSLIDKSLVVTAPAAEPGADGEMRYRLLETVAEYAAERLDESGERAAVERRHLVAYRELARTADPLLRGPAQRHWMIRLETEHENLRTALRRAVAARDEQEALCLVLSLGWFWHLRGHRAESRHWATAAAELGPSPFAPPVAPAPPLHISCTAAPPPMEPELLVEARRGVRLFALANIEGDLQAVVGEDTQRELEGIVAAYRAGLPQTCRVPGVLWFFAVVLKGDLGMLREMADESVRTCRELGYEWELAFTLQLRARIYNERSGENEGAIRDADEALEIFRRIGDTWGAAEALAGRGETREQRGEGAAAAADYRAAIRCAQDLGAHEQVLWLRARLAGVFVEFGDEEEAAKGERMLREVVEQGPQVGAEALAYARVHLAQHCGTTGRVGEARALLVTLHGEFERRALKLFEGMAEGMLAWVDLLEGRPDDALATVRGGLVKTSGRMTGLIAPFIPVTQLLTAAEALSALGGPERAETAARLAGAYDTLRKPQYYRRSAIERTGRERTETAARAELGDAAYERVHAEGMGLTLEEAVALV
>NZ_CP023992.1|WP_099013510.1|2838087_2838633_-|Uma2-family-endonuclease
MTSAEDRAVELQEQIRLPRSMRLRLTRNGLTLVPITQAHLTTQRRILNQIEERLPGWTPVGEFGVLPPREGYTPEPDASAVPTDKLLPDASKFPEDLLRFVVEVVSPESEERDYSTKSDHYALRGIEAYLVVNVLTARWTLLTRPQGGTYRHAVTDDFGEKIEIPVEDQTLVLDSSQFMRV
>NZ_CP023992.1|WP_079257362.1|2838785_2839583_+|site-2-protease-family-protein
MTTAISRRDRRISPVFLGLFAIMVVSAWAVWTEYSASPGFAVFLFVVSGWIVSLCLHEYAHARTALHGGDLSIGAKGYLTLNPLKYTHVALSIVLPVIFVIMGGIGLPGGAVFIERHRIQGRWKHSVISAAGPLTNVLFAAALTAPFWLGATDQVPELFRYALAFLALLQVTAAILNFLPVPGLDGYGVIEPWLSYRIRRQVEPYAPFGLLAVFGILWIPEVNQAFFNAVDALMRALGVTEWDTYWGQEFFRFWQGEPDIAGFRS

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Crispr_ID: NZ_CP023992_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_5

3121089-3121192

Orphan

Consensus_repeat	Method
TGCTCTGCCAATTGAGCTACAGGGGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_5

>merge|NZ_CP023992|5|3121089-3121192|CRISPRCasFinder
TGCTCTGCCAATTGAGCTACAGGGGACCGAGCTCCCCCGACTGGACTCGAACCAGTAACCTGCCGGTTAACAGCCGGCTGCTCTGCCAATTGAGCTACAGGGGA

>NZ_CP023992|5|5|3121089-3121192|CRISPRCasFinder
TGCTCTGCCAATTGAGCTACAGGGGA	CCGAGCTCCCCCGACTGGACTCGAACCAGTAACCTGCCGGTTAACAGCCGGC
TGCTCTGCCAATTGAGCTACAGGGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_099013658.1\|3131102_3133415_+\|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl\|CDD\|239155
NZ_CP023992.1\|WP_099013657.1\|3128612_3129974_-\|deoxyguanosinetriphosphate-triphosphohydrolase	unknown	unknown	gnl\|CDD\|235098
NZ_CP023992.1\|WP_161370925.1\|3113931_3114894_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|226951
NZ_CP023992.1\|WP_099016912.1\|3129970_3130804_-\|sirohydrochlorin-chelatase	unknown	unknown	gnl\|CDD\|225049
NZ_CP023992.1\|WP_099013655.1\|3121736_3123236_+\|sugar-kinase	unknown	unknown	gnl\|CDD\|198375
NZ_CP023992.1\|WP_069866126.1\|3113221_3113929_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP023992.1\|WP_069866118.1\|3117009_3117648_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378822
NZ_CP023992.1\|WP_069866322.1\|3133446_3134433_-\|adenosine-deaminase	unknown	unknown	gnl\|CDD\|236480
NZ_CP023992.1\|WP_069866116.1\|3117793_3118234_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|366361
NZ_CP023992.1\|WP_069866104.1\|3127035_3128331_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|170080
NZ_CP023992.1\|WP_167460013.1\|3134624_3135251_+\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|99749
NZ_CP023992.1\|WP_069866122.1\|3115668_3116037_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380301
NZ_CP023992.1\|WP_099013652.1\|3112688_3113099_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237381
NZ_CP023992.1\|WP_099013656.1\|3124972_3126961_-\|DNA-primase	unknown	unknown	gnl\|CDD\|235551
NZ_CP023992.1\|WP_069866120.1\|3116033_3116873_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|212668
NZ_CP023992.1\|WP_069866112.1\|3121441_3121711_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099016911.1\|3123373_3124654_-\|RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|235640
NZ_CP023992.1\|WP_069866326.1\|3115287_3115617_+\|molecular-chaperone-DnaK	unknown	unknown	gnl\|CDD\|274340
NZ_CP023992.1\|WP_099013654.1\|3119571_3120594_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP023992.1\|WP_099013653.1\|3118318_3119290_+\|nitronate-monooxygenase	unknown	unknown	gnl\|CDD\|240081

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_099013658.1\|3131102_3133415_+\|molybdopterin-oxidoreductase-family-protein	gnl\|CDD\|239155	cd02754, MopB_Nitrate-R-NapA-like, Nitrate reductases, NapA (Nitrate-R-NapA), NasA, and NarB catalyze the reduction of nitrate to nitrite. Monomeric Nas is located in the cytoplasm and participates in nitrogen assimilation. Dimeric Nap is located in the periplasm and is coupled to quinol oxidation via a membrane-anchored tetraheme cytochrome. Members of the MopB_Nitrate-R-NapA CD belong to the molybdopterin_binding (MopB) superfamily of proteins.	0
NZ_CP023992.1\|WP_099013657.1\|3128612_3129974_-\|deoxyguanosinetriphosphate-triphosphohydrolase	gnl\|CDD\|235098	PRK03007, PRK03007, deoxyguanosinetriphosphate triphosphohydrolase-like protein; Provisional.	0
NZ_CP023992.1\|WP_161370925.1\|3113931_3114894_-\|HAMP-domain-containing-protein	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.39122e-57
NZ_CP023992.1\|WP_099016912.1\|3129970_3130804_-\|sirohydrochlorin-chelatase	gnl\|CDD\|225049	COG2138, COG2138, Sirohydrochlorin ferrochelatase [Inorganic ion transport and metabolism].	2.74934e-28
NZ_CP023992.1\|WP_099013655.1\|3121736_3123236_+\|sugar-kinase	gnl\|CDD\|198375	cd07809, FGGY_D-XK_1, D-xylulose kinases, subgroup 1; members of the FGGY family of carbohydrate kinases. This subgroup is composed of D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17) from bacteria and eukaryota. They share high sequence similarity with Escherichia coli xylulokinase (EcXK), which catalyzes the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. Some uncharacterized sequences are also included in this subfamily. EcXK 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+ might be required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	1.56159e-112
NZ_CP023992.1\|WP_069866126.1\|3113221_3113929_-\|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].	3.10377e-73
NZ_CP023992.1\|WP_069866118.1\|3117009_3117648_+\|hypothetical-protein	gnl\|CDD\|378822	pfam12158, DUF3592, Protein of unknown function (DUF3592). This family of proteins is functionally uncharacterized.This family of proteins is found in bacteria, archaea, eukaryotes and viruses. Proteins in this family are typically between 150 and 242 amino acids in length.	0.000229668
NZ_CP023992.1\|WP_069866322.1\|3133446_3134433_-\|adenosine-deaminase	gnl\|CDD\|236480	PRK09358, PRK09358, adenosine deaminase; Provisional.	3.51467e-150
NZ_CP023992.1\|WP_069866116.1\|3117793_3118234_+\|VOC-family-protein	gnl\|CDD\|366361	pfam00903, Glyoxalase, Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily.	3.03507e-13
NZ_CP023992.1\|WP_069866104.1\|3127035_3128331_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|170080	PRK09754, PRK09754, phenylpropionate dioxygenase ferredoxin reductase subunit; Provisional.	1.24477e-67
NZ_CP023992.1\|WP_167460013.1\|3134624_3135251_+\|Uma2-family-endonuclease	gnl\|CDD\|99749	cd06260, DUF820, Domain of unknown function (DUF820). This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. They have been predicted to belong to the PD-(D/E)xK superfamily of nucleases.	1.26262e-12
NZ_CP023992.1\|WP_069866122.1\|3115668_3116037_+\|hypothetical-protein	gnl\|CDD\|380301	NF033459, DksA_like, RNA polymerase-binding protein DksA.	3.4349e-10
NZ_CP023992.1\|WP_099013652.1\|3112688_3113099_-\|hypothetical-protein	gnl\|CDD\|237381	PRK13419, PRK13419, F0F1 ATP synthase subunit A; Provisional.	0.0027588
NZ_CP023992.1\|WP_099013656.1\|3124972_3126961_-\|DNA-primase	gnl\|CDD\|235551	PRK05667, dnaG, DNA primase; Validated.	0
NZ_CP023992.1\|WP_069866120.1\|3116033_3116873_+\|hypothetical-protein	gnl\|CDD\|212668	cd10225, MreB_like, MreB and similar proteins. MreB is a bacterial protein which assembles into filaments resembling those of eukaryotic F-actin. It is involved in determining the shape of rod-like bacterial cells, by assembling into large fibrous spirals beneath the cell membrane. MreB has also been implicated in chromosome segregation; specifically MreB is thought to bind to and segregate the replication origin of bacterial chromosomes.	2.47137e-14
NZ_CP023992.1\|WP_099016911.1\|3123373_3124654_-\|RNA-polymerase-sigma-factor	gnl\|CDD\|235640	PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.	2.29291e-164
NZ_CP023992.1\|WP_069866326.1\|3115287_3115617_+\|molecular-chaperone-DnaK	gnl\|CDD\|274340	TIGR02890, conserved_hypothetical_protein, regulatory protein, yteA family. Members of this predicted regulatory protein are found only in endospore-forming members of the Firmicutes group of bacteria, and in nearly every such species; Clostridium perfringens seems to be an exception. The member from Bacillus subtilis, the model system for the study of the sporulation program, has been designated both yteA and yzwB. Some (but not all) members of this family show a strong sequence match to Pfam family pfam01258 the C4-type zinc finger protein, DksA/TraR family, but only one of the four key Cys residues is conserved. All members of this protein family share an additional C-terminal domain. Smaller proteins from the proteobacteria with just the N-terminal domain, including DksA and DksA2 are RNA polymerase-binding regulatory proteins even if the Zn-binding site is not conserved. [Unknown function, General].	1.33142e-14
NZ_CP023992.1\|WP_099013654.1\|3119571_3120594_+\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	5.75225e-29
NZ_CP023992.1\|WP_099013653.1\|3118318_3119290_+\|nitronate-monooxygenase	gnl\|CDD\|240081	cd04730, NPD_like, 2-Nitropropane dioxygenase (NPD), one of the nitroalkane oxidizing enzyme families, catalyzes oxidative denitrification of nitroalkanes to their corresponding carbonyl compounds and nitrites. NDP is a member of the NAD(P)H-dependent flavin oxidoreductase family that reduce a range of alternative electron acceptors. Most use FAD/FMN as a cofactor and NAD(P)H as electron donor. Some contain 4Fe-4S cluster to transfer electron from FAD to FMN.	6.18724e-78

>NZ_CP023992.1|WP_099013654.1|3119571_3120594_+|alpha/beta-hydrolase
MGTRIGKTNTFAALIAALVTVLVISLGASSGAWGESRGHGTATKQSPSPYPKVKPPPGFQSKYANVNGFRMHYLRGGKGSPVVLIHGFPQSWAEWRDQMGPLSKNHTVIAVDLRGAGNSEVTKSGYQKAQMARDVHELLRRLKLNDGVQVVGHDVGLWVSYAYAAQWPSEVRRMAVMEAPIPDDSLYRFPALEANPKTPSMWHFGLFQLPLAEQLISGHERVFVRGFIGELLVNKSAFTPADYDFYAHYLKQPGRTLAWMRMYRQLREDVQQNKKFLAEGKLRMPILAIGGQASFGGKIADQWRDYAMNVHGRVVKGSGHWVTEEKPREVTAMLQSFLRK
>NZ_CP023992.1|WP_099013653.1|3118318_3119290_+|nitronate-monooxygenase
MFGITHPVMAAPMGLHSGGTLAAAVSAAGGLGSFAGTHPWKGPDWIHAEIATIRATTDRPFGVGFITPFLPFTEPHFDAALEERPEIIALSFADPRPWLARAKDAGARVVCQVQNYEDAEVAVAAGADVLVAQGSEAGGHTGTMGLLPFLAGIVRRHPDVPVLAAGGIGDGRTLAAVLTAGADGAWLGTAFLATPEAVEVHDAHKRLIVESDGGDTVWTRTYNIVSGLPWPETLGERVRRNRFTDEWSERESTLQNRRAEFAPPEDVSPVEAPPDPDTSEIIYGQSACFVDAVRPAADVVRTISEEAEAILASRPRSLRTAVR
>NZ_CP023992.1|WP_069866116.1|3117793_3118234_+|VOC-family-protein
MTAPRDVPAPEQGLVLTHFLTVRDVARSRRFYADILGGEVVLEENPAIVKVANSWIIMNPGGGPTPDKPGITLVPPDDGDTVSSFLNVRVADIGAFYAAAVAKGAEFLTEPIDRKAELRCYLRDPDGYLIEVGQATGLLRGVFADR
>NZ_CP023992.1|WP_069866118.1|3117009_3117648_+|hypothetical-protein
MSGVIPPAQPPPDPRHDKPVHPLSLWRWRHNPLYRYTDRLQGWIALALLLLVPVLGLGAMFVAGGAAQHHYRAAAEHRKETLHRTTAVLTHDAPGHPEPGSAEARETRYPATVRFTDPDGRTRTAKADVLPGLAAGSSVHVWVDKDGAIAEPPMPDAQIRSRTMGWALIAFVTVTLAGAAVYRCTTVVLRRRNLAEWDTEWAETAPRWTTSP
>NZ_CP023992.1|WP_069866120.1|3116033_3116873_+|hypothetical-protein
MTVIRRLRAGSRIRHRHRPWPLCRHCCGLALDMGSARTRAWIAGRGTIIDVPTITFPGAGAVHPIQRGAIVDVPGTARMLDRLLSRRLPRLTRPLVVVTAPVLDGPAYRERARTAVEVLRPRAVLTVPTARAIALAANADLSLPLLVVDIGAHLTEVVLLVDGIVFDARRTALGTTDLADAGATAEISEAITSMITSMLRQDRTSLTADALSRGALLAGGGALRPDLTRRLIGGLHAPLRAVPAPHTAAVRGAAKILQAAHAHPSAGGTSPPGPGPLSR
>NZ_CP023992.1|WP_069866122.1|3115668_3116037_+|hypothetical-protein
MVNHQTMGDRAAHLSPEDLAALRENLHEQRLFRQEQLRRIASAPRAEDLLRRRSAAQAEVHVKLAASARMVLADVEAALQRIAEGSYGACHLCRRPVERERLMIVPQARYCGRCQQVREAGR
>NZ_CP023992.1|WP_069866326.1|3115287_3115617_+|molecular-chaperone-DnaK
MSLDTAETGPRPGRLTAHEARQRLEHARNSRLAQLQALKETGQSTDDHLVSAQTEAIQRVLTEIDEAFARVDDGSYGTCQGCSKPVPAERLEILPYTRHCVACQRRAAA
>NZ_CP023992.1|WP_161370925.1|3113931_3114894_-|HAMP-domain-containing-protein
MSLFWRIFGLNAVVLGTATALLLWAPVTVSVPVLLTEAIILVGGLAVMLVANGTLLRWGLAPLERLTRLMTTVDLLRPGQRLPVPGAGAGSEVSELIRTFNAMLDRLEHERATASARVLLAQEAERRRIAQELHDEVGQSMTAILLVLKRAADDAPEPLREDLQQAQEITRESLDEVRRLVRRLRPGVLDDLGLVSALTSLTQDFATHTGLRVVRRLDADLPALDPESELVLYRVAQESLTNVARHADAHRVEVSLHRSGEAVVLEMTDDGRGIEAACEGAGIRGMRERALLAGATLDITSTPGTGTRIRLITPVPRKQP
>NZ_CP023992.1|WP_069866126.1|3113221_3113929_-|response-regulator-transcription-factor
MHDPTPTEPTAAPAPSPGTAAPIRILLADDHALVRRGVRLILDREPDLEVVAEAGDGAEAIEAARNQEIDLAVLDIAMPRLTGLQATRELAALKPGLRILMLTMHDNEQYLFQALKAGACGYVLKSVADRDLVAACRAAMRNEPFLYPGAVTALIRTYLDRVRHGEEDSDQLLTPREEEVVKLVAEGHSSKEIAEMLFISVKTVHRHRSNILHKLGLHDRLELARYAIRAGLIEP
>NZ_CP023992.1|WP_099013652.1|3112688_3113099_-|hypothetical-protein
MRPAPRTIPPAGHRLAGMLVVLLAVLLALVPADTARAASAAPAPHPAPAATSAERPDTAPHADDAWAAARAAWARARHDHLGERPSLPDHHATHPRGTDTGPAAGTRTAGPCACAPVPSDRWAQQRGRAPPASPGT
>NZ_CP023992.1|WP_069866112.1|3121441_3121711_+|hypothetical-protein
MRYRLTFITGMAVGYVLGTRAGRERYEQLRACAQKLAQNPAVRNTAESAAQGGRQAAVKALDKVRPLREKIGQRDARAVREDDWGTSNT
>NZ_CP023992.1|WP_099013655.1|3121736_3123236_+|sugar-kinase
MGIVAGLDSSSESTRIVVCDTDTGAVIKQGYAPHPVGGSGDVDPQTWLMSLGEAAEGGLLEGVQAIGVSAQQHGLLALDAGGVLVRPASMGNDKRAQSAAADLTEALGGRTAWAQAVGAVPTASQPVAKLRWLARNEPESAHRVAELMQPHDWLVWQLLGRPMRRTTDRGTASSSGYWSAASGSWRPDLVQLALGHQVRLPEVIGPADAAGHTPEGLLISAGTGETMAAAFGLGVGIGDAVISLGASGSVFSVHHEALADPTGTILSYADATGMHLPVVHTLNAVRTLRGTAELLSTDLEGLSALAMKSTPGSYGLVFLPYLEGERTPHLPHTAGTLTGLRRESMKPEHLARAAFEGMLCGLADALDVLRGRGVQVRRVFLLGPAADLQAVRAIAPALLGAQIVVPQPADYAALGAARQAAWALGVSHGTQSPHEPPRWPAAASQVFEPGEDLPVGQSVRQQYVAVREQTHPGAFEPGVFEPGAQEAMGHEAVGEYGAM
>NZ_CP023992.1|WP_099016911.1|3123373_3124654_-|RNA-polymerase-sigma-factor
MPDRSAPSAAITLEVAPVQTQTLTDAAPSPHPRSPHPPHATAVAPTVPEDSTELAPEGVPDTGQDAAPDPLADLGPDTVSGPAADGAPEAEPEEPAGPTEPVEAVEAEEPVEPVGPPARADSSGPSADLFRQYLREIGRIPLLSAVEEVELARRVEAGLFAEEKLGNASDLDTQLALDLDRLVVLGRMAKRRLIEANLRLVVSVAKRYVGRGLTMLDLVQEGNLGLIRAVEKFDYARGYKFSTYATWWIRQAMSRALADQARTIRVPVHVVELINRVVRVQRRMLQERGYEPTPEEVAAHLDLLPERVSEVLRLAQEPVSLHAPVGEEDDVALGDLIEDGDAASPVESAAFLLLREHLEAVLSTLGERERKVVQLRYGLADGRPRTLEEIGRIFGVTRERIRQIESKTLNKLRDHAFADQLRGYLD
>NZ_CP023992.1|WP_099013656.1|3124972_3126961_-|DNA-primase
MAGRINDDDVKAVRAAVPIDAVVSEYLQLRNAGGGNLKGLCPFHDEKSPSFQVSPSKGLYYCFGCQEGGDTVDFIMKIDHLSFAETIERLASQAGITLRYEEGGYTPGRQQGERTRLVEAHKAAAQFYIEQLDGPEAEIGRTFLAQRGFDQAAAQHFGVGYSPAGWDHLVRYLRGRGFTDKELILSGLVQEGRRGPIDRFRGRLMWPIRDISGEVVGFGARKLRDDDNGPKYLNTPETPLYRKSQVLYGIDLAKKDIAKSSRAVVVEGYTDVMACHLAGVTTAIATCGTSFGGDHIKILRRLLMDNSGAEVVFTFDGDAAGQKAALRAFEDDQRFAAETSIAITPDGMDPCELRLARGDEAVADLVESRTPLFAFALKSIVSRYNLDTEEGRIAAVDEAVPVVAAIKNPGLRDRYAIRLIGMVGIATQAEEQSIIRRVRGLARSRQNGGPEHGGRGDQRGGGPGGSRYGGRGDQRGGGPGGPAGPGGPGGPGAAGAPPVPRGPALNLRSPAHRVERELLKLALQHPHLVSPAFDAYGIDEFTAPPYAAVRRAIEDAGGAAAADADYLARVREAAPDDTVRAMVTELAVEPPHTRRDPDEIYAGVQLVAVRLAAVNHRVTEVRGALQRLGQHADPAHLAAVQNELWVLQQYGQSLRDRGAAAL
>NZ_CP023992.1|WP_069866104.1|3127035_3128331_-|FAD-dependent-oxidoreductase
MVDAHQTFVIVGGGLAGAKAAETLRAEGFTGRVILICDERDHPYERPPLSKGFLTGSQERDSVFVHEPAWYAQSDIELHLGLPAVHLDRAAKAVTLGDGARVHYDRLLLATGAEPRRLDIPGTDLAGVHHLRRLAHAERLKGVLTALGRDNGQLVIAGAGWIGLEVAAAARGYGAEVTIVEPEPTPLHPVLGPELGALFADLHGEHGVRFHFGARLTEITGQDGMVLAALTDDGEEHPAHSVLAAIGAAPRTALAEAAGLEVVDRAAGGGIAVDASLRTSDPDIFAAGDAASAPLAFLEGTPVRAALPPSARLRVEHWANALNGGPAAARAMLGQDVAYDRVPYFFSDQYDVGLEYSGYAPPGSYDQVLVRGDVGKRQFIAFWLNDGRLLAGMNVNVWDVTESIQRLIRGGHQLDPAALADPSVPLNSLLT
>NZ_CP023992.1|WP_099013657.1|3128612_3129974_-|deoxyguanosinetriphosphate-triphosphohydrolase
MSPSAPPEPDPAPWAGAPEADTRRVPGYAAADLERWAPEPDKRPGRTAFQRDRARVLHSAALRRLAGKTQVVPAAPAADPGPAGRAPAFDGTPRTRLTHSLECAQVGRELGAALGCDPDLVEMACLAHDLGHPPFGHNGERVLNEIAEPCGGFEGNAQSLRLLARLEPKRFVPDRKTGEPVSVGLNLTRAALDAATKYPWPRGGHPHSPGSPKFGVYEDDIPIFEWYRQGAPEGRTTFEAQVMDWSDDVAYSVHDVEDGLHAGHLDPASLLSGPERREVFAVAADRYAPGAEPGELAEALDRLLGQEWWPHGYDGSSVAQARLKDATSQLIGRFCLAAEGATRAAYGTGRFTRYHAELVVPRAIHLECAVLKAVADRYVIQRADQELLRADQRVVIAELGAALIARAPDGLDPQFRGLFDAAGDDRGRLRSIVDQIASLTDTSARGLHARLTV
>NZ_CP023992.1|WP_099016912.1|3129970_3130804_-|sirohydrochlorin-chelatase
MTRFTAQLTTQLDRLGAHGVRRGRRDRPPTLVAVAHGSRDPEALSTVTALLDRVRALRPGLPVHLGHIELNQPLLSDTLAALRGEVVLVPLLLSRGYHIKQDIPDAVAAAPHLTARIAAPLGPDPLLAEALDARLAEAAYAWPMEAGRQTPAPHRAGVVLAAAGSRDPDAAADTARTAALLGARLGGVPVLPGYASGSGPTVPEAVRALAALGRDRIAVASYFTAPGRFATQCANAAPGVAAAPLGAHPAVARLVLRRYEQALASAPLPHPAATVGV
>NZ_CP023992.1|WP_099013658.1|3131102_3133415_+|molybdopterin-oxidoreductase-family-protein
MAYVPGEHSPASDPVDTHCPYCSLQCGMALRPVAPDGGPVGVEVVERTAFPVNRGALCGKGRTAPAVLSSRVRLTEPLVRRPDSGRLEPATWEEALDRIAEGLAAIGRAYGRDAVGVFGGGGLTNEKAYALGKFARVVLGTSQIDYNGRFCMSSAAAAHQRAFGLDRGLPFPLADVARTGCVVLVGSNLAETMPPALRHLTELKEAGGRLIVVDPRRTRTAEQADLHLAPRPGTDLALALGLLHLVVAEGRVDEEFVERRTSGWPEARAAAMAHWPELVERITGVPVPELRKAVTMFCGAENSMVLTARGPEQQSKGTDTVGAWINLCLATGRAGRPLSGYGCLTGQGNGQGGREHGQKADQLPGYRKLDDPAARAHVAAVWGVEPDALPGPGRSAYELLDALGGDVRALLLMGSNPLVSAPRAAHVESRLRSLDFLAVADVVLSETAALADVVLPVAQWAEETGTMTNLEGRVVLRRAALTPPPGVRTDLQVLGGLAARLGWEKGFPADAEEVFEELRRASAGGPADYSGITYRRIAEEDGVFWPCPERTERMEGAGAGAAGTEADGSEGAGRADSVAAESADPECAERAQCAERADPDGSKGTGSGGAGRAGGPHPGTPRLFLDRFATDDGRARFAPVGHRPAAEEPDAEYPVLLTTGRVLAQYQSGAQTRRVAELNEAAPGPYVQLHPRLAERLGAVEGAPIAVVSRRGRAVAPARISRDIRPDTVFMPFHWAGPGRANTVTNPALDPVSRMPEFKVCAVRLELSEG
>NZ_CP023992.1|WP_069866322.1|3133446_3134433_-|adenosine-deaminase
MPPIPTAELHLHIEGTLEPDLAFALAGRNGVELPFATREELRAAYSFGDLQDFLNLYYALMTVLRTEDDFADLTDAYLARARAQGVRHAEIFFDPQAHTARGVEIDTVIRGIGRALDAAPRTYGITTRLIMCFLRDESAESALATFEAARPHLDRIAAVGLDSAEVGHPPSKFREVYALAREAGLKCVAHAGEEGPPAYVWEALDVLGVDRVDHGVRSLEDEALVARLVADRTPLTVCPLSNVRLRVVDRLQDHPLPAMLDAGLLVTVNSDDPAYFGGYVGDNYTAVRDALGLDEATLRTLARNSFQAAFLDEETRAGYLKEVEGWAR
>NZ_CP023992.1|WP_167460013.1|3134624_3135251_+|Uma2-family-endonuclease
MTTENTPAAEQPREEPLKGFEELLRATEELDTPDGYKAELIRGKIVVSPWSRLPYLWPMRELRLRLEPHAPKGHIAETSPFLFTFPSDERAFGPDLFIADGKAFRGVEGRHADSEALSLVAEFTSVSTRDVDWQEKLEVYGRHVPVYLVVDMQAEEITAFWDPSDRGYHARMTVPFGKPLTIPVPFDFELDTNIFLETEEPEEEETTE

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Crispr_ID: NZ_CP023992_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_6

3501741-3501834

Orphan

Consensus_repeat	Method
GTCCTCAAACGCCGGACGGGCTTGAATTGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_6

>merge|NZ_CP023992|6|3501741-3501834|CRISPRCasFinder
GTCCTCAAACGCCGGACGGGCTTGAATTGCCCCACCGGCCACGGGCTCCGCCCCAAGACCCTGGTCCTCAAACGCCGGACCGGCTTGAATTGCC

>NZ_CP023992|6|6|3501741-3501834|CRISPRCasFinder
GTCCTCAAACGCCGGACGGGCTTGAATTGCC	CCACCGGCCACGGGCTCCGCCCCAAGACCCTG
GTCCTCAAACGCCGGACCGGCTTGAATTGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_079152982.1\|3603032_3603692_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP023992.1\|WP_099013784.1\|3484914_3494535_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_099013788.1\|3537766_3563566_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_099013790.1\|3574018_3598642_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_099013786.1\|3516689_3532442_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_167460018.1\|3563591_3573926_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_099013778.1\|3453902_3454112_-\|DUF397-domain-containing-protein	unknown	unknown	gnl\|CDD\|377231
NZ_CP023992.1\|WP_099013782.1\|3455738_3467447_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_142881432.1\|3455115_3455454_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_079257701.1\|3600482_3600992_-\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|225937
NZ_CP023992.1\|WP_099013776.1\|3449661_3449826_-\|FxLD-family-lantipeptide	unknown	unknown	gnl\|CDD\|275157
NZ_CP023992.1\|WP_099013781.1\|3455453_3455669_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013779.1\|3454108_3454963_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP023992.1\|WP_069864140.1\|3598941_3600486_-\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|225962
NZ_CP023992.1\|WP_099013787.1\|3532706_3537701_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP023992.1\|WP_099013775.1\|3446553_3449592_-\|lantibiotic-dehydratase	unknown	unknown	gnl\|CDD\|377403
NZ_CP023992.1\|WP_069864134.1\|3601061_3601628_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013777.1\|3452158_3452626_+\|NUDIX-hydrolase	unknown	unknown	gnl\|CDD\|239217
NZ_CP023992.1\|WP_079152983.1\|3601795_3603040_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP023992.1\|WP_099013783.1\|3467509_3484858_-\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_079152982.1\|3603032_3603692_+\|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].	3.51493e-76
NZ_CP023992.1\|WP_099013784.1\|3484914_3494535_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_099013790.1\|3574018_3598642_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_099013788.1\|3537766_3563566_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_167460018.1\|3563591_3573926_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_099013778.1\|3453902_3454112_-\|DUF397-domain-containing-protein	gnl\|CDD\|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	1.12511e-21
NZ_CP023992.1\|WP_099013782.1\|3455738_3467447_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_099013786.1\|3516689_3532442_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_079257701.1\|3600482_3600992_-\|PH-domain-containing-protein	gnl\|CDD\|225937	COG3402, COG3402, Uncharacterized conserved protein [Function unknown].	1.6627e-20
NZ_CP023992.1\|WP_099013776.1\|3449661_3449826_-\|FxLD-family-lantipeptide	gnl\|CDD\|275157	TIGR04363, hypothetical_protein, FxLD family lantipeptide. Members of this protein family occur with a cassette of lanthionine-type peptide modification enzymes. Members are small (about 60 amino acids long), rich in Cys, and variable in copy number per genome (from one to three). These features suggest that members of this family are modified to become lantipeptides, although not necessarily a lantibiotic. There is no GlyGly cleavage motif to separate a leader peptide from core region.The considerable abundance in Streptomyces and relatively strong consideration hints at a non-antibiotic function. The motif FxLD in the N-terminal region is nearly invariant.	3.01301e-07
NZ_CP023992.1\|WP_099013779.1\|3454108_3454963_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	3.43763e-11
NZ_CP023992.1\|WP_069864140.1\|3598941_3600486_-\|PH-domain-containing-protein	gnl\|CDD\|225962	COG3428, COG3428, Predicted membrane protein [Function unknown].	4.83881e-47
NZ_CP023992.1\|WP_099013787.1\|3532706_3537701_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP023992.1\|WP_099013775.1\|3446553_3449592_-\|lantibiotic-dehydratase	gnl\|CDD\|377403	pfam04738, Lant_dehydr_N, Lantibiotic dehydratase, C-terminus. Lantibiotics are ribosomally synthesized antimicrobial agents derived from ribosomally synthesized peptides. They are produced by bacteria of the Firmicutes phylum, and include mutacin, subtilin, and nisin. Lantibiotic peptides contain thioether bridges termed lanthionines that are thought to be generated by dehydration of serine and threonine residues followed by addition of cysteine residues. This family constitutes the N-terminus of the enzyme proposed to catalyze the dehydration step, via glutamylation of the substrate during lantibiotic biosynthesis. The enzyme dehydrates Ser/Thr residues in the precursor by glutamylation.	0
NZ_CP023992.1\|WP_099013777.1\|3452158_3452626_+\|NUDIX-hydrolase	gnl\|CDD\|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	2.06392e-15
NZ_CP023992.1\|WP_079152983.1\|3601795_3603040_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.57386e-53
NZ_CP023992.1\|WP_099013783.1\|3467509_3484858_-\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0

>NZ_CP023992.1|WP_099013784.1|3484914_3494535_-|type-I-polyketide-synthase
MVNNEDKLRDYLKRATADLRQARRQLREVEERHQEPIAIVAMSCRYPGGVTTPEELWRLVLDGQDAISGFPTDRGWDVESLYDADPDQAGASYVDEGGFLYDAGGFDPAVFGISPREAMAMDPQQRLLLEASWEAFERAGIDPTGLRGHRTGVFAGVMYHDYTSRLDSVPEGVEGFLGTGSSGSIASGRVSYTFGLEGPAVTVDTACSSSLVTLHMAVQALRNGECSLALAGGVTVMATPSTFTEFSRQRGLAADGRCKPFAAAADGTGWGEGVGMLLVERLSDARKNGHPVLAVVRGSAINQDGASNGLTAPNGPSQQRVIHQALTNGRLSAADVDAVEAHGTGTTLGDPIEAQALLATYGQEHTEDQPLLLGSIKSNIGHTQAAAGVAGIIKMVKAIEHGVLPRTLHIDEPTPHVDWSAGAVSLLAETTPWPETGRPRRAAVSSFGFSGTNAHTILEQAPAEEPAEDATEEPAPAKPLDVVPWALSGKSAAALRAQAERLLAHLEADPSLSPLDVALSLTTTRAQLDHRAVVRGQDRDTLMAGLTALAEGGMAAGVAQGSAVGGRTAFVFPGQGSQWAGMAVGLMDASPVFAAWIEECAGALGEFTDWSLVDVLRGAEGAPSLERVDVVQPVLFAVMVSLAELWRSLGVVPAAVIGHSQGEIAAACVAGALSLRDAARVVALRSQAIGRVLAGKGGMVSVALPVVEVRERIALWGEERISVAAVNGPSSVVVSGEPEALDELIASCEADEVRARRVPVDYASHSAQVELLREELLELLAPVEPKTAEVPFLSTVTGEWVEGPELDAEYWFTNLRRTVELEGAVRRLLDEGFGAFIESSAHPVLTMGVQETAEDAGREAAAIGSLRRDEGGLDRFWASVGEAWTRGVTVDWDGVFDGTGAVRVELPTYAFQHQHYWLESGTPTADATPAADPVEARFWEAVEREDWQSLAAELDVDGDERVSALLPALASWRKQAREQSTVDGWRYRVTWKPLADGQSARLTGVWLVVAPATENTDTWTDAVAGVLAERGADVRRIAVDTGVDGREELTERLRAALAETDGIPFTGVLSLLALDGHPHPRHPSVPAGVAAQLALVQALGDAEIGAPLWSATRGAVSVGRAEPLESPEQALVWGLGRVAALEHGERWGGLVDLPGAPDERALARLVTALAGAEEEDQVAIRATGLLVRRLVRAPLAATPAVRTWEPTGTTLVTGGTGALGAHVARWLAGNGAEHLVLTSRRGLDAPGAADLRSELTELGAKVTIAACDVADRAQVEALLADIPAEHPLTAVVHTAAVLDDGVIEGLTPDQVDRVLKVKVDATRHLHELTRDLDLSAFVLFSSFAATFGAPGQGNYAPGNAFLDAFAEYRRAQGLPATSLAWGPWGEGGMAEGGVGDRMRRHGVIEMAPRSAVTALQHALDRDESVLTVVDMEWKRFVLAFTSGRSRPLLHDLPEARDVIQDMAGDADADGAGAVALTQQLAGVPEAEQERLVLELVRTAVAAVLGYAGADDVEAGRAFKELGFDSLTAVELRNRLSSASGLKLPPTLIFDYPTPTVLARHLRGEIAGERSAAVAALPTAAALADDEPIAIVSMSCRFPGGVRTPEELWQLLVSGGDALSEFPGDRGWDTEALYNPDPDAQGTSYTREGGFLTGAGEFDPTFFGISPREAMAMDPQQRLLLEASWEAFERAGIDPATLHGSPSGVFVGTNGSDYSILMRSNTEGYEGHLATGSAASVVSGRLSYTFGLEGPAVTVDTACSASLVALHLAVQSLRQGECSIALAGGVTVMATPGTFIEFSRQRGLSSDGRSKAFSADADGFSPAEGVGMLLVERLSDARKNGHPVLAIVRGSAINQDGASNGLTAPNGPSQQRVIRQALANARLSAAEVDVVEAHGTGTTLGDPIEAQALLATYGQERPEGQPLLLGSIKSNIGHAQAAAGVAGVMKLVLALRHGVLPESLHIVEPTPHVDWSAGEVELLTEAREWPETGRPRRAAVSSFGFSGTNAHAIIEQAPAEEPDGAEPVTRRPGALPWTVSGKSEAALRAQAGKLLAHLDADPAPRPLDIGHALATTRAAFDRRAVLVGTDRDDFARGLDALARGQVVPNLVQGDSIGGKAAFVFPGQGSQWVGMAVELLDASPVFAARIDECAAALAEFTDWSLVDVLREAEGAPSLERVDVVQPVLFSVMVSLAELWRSLGVRPSAVVGHSQGEIAAACVAGILPLQDAARVVTLRSQAIGRVLAGKGGMVSVALPVAEVRERIEPWGEERISVAAVNGPSSVVVSGEPEALDELVASCEADEVRARRVPVDYASHSAQVELLRDELMELLAPVRPKAAEVPFLSTVTGEWVDGTELDAEYWFTNLRRTVELEGAIRRLLDEGFGMFIESSAHPVLTMGVQETAEDAGREAAAIGSLRRDEGGLDRFWVSLGEAWTRGVNVDWEAVYEGTGAVRVELPTYAFQHQTYWPRAADVPADESGTPSDAVDARFWEAVEREDLESLADTLAFGDDGERSSLGAVLPALASWRKQAREQSTVDGWRYRVTWTSLTERQAPRLSGTWLLAVPESAATDDWTLGAIRMLAERGAEVRQITPTAVESDRASLTRLVREELADAGTVSGVLSLLAFDEGTAPGTDGVNAGLTGTAVLTQALGDAGVDAPLWCATRGAVAVGRTDTVDSPEQALVWGLGRTAALEYPERWGGLVDLPGAPDERALARLAGVLAGTDGEDQLAVRTAGVFARRLVHAPLAGAPAAGAWKPAGTTLVTGGTGALGAHVARWLAANGAEHLVLTSRRGLEAPGAAELRDELTGLGSEVTVAACDVADRKAVETLLATIPADQPLTAVMHAAGVLDDGVLDALTPERFATVLGPKADAARHLHELTRELDLSAFVLFSGIAGTLGDAGQGNYAAANAYLDALAERRRADGLPATSVAWGRWGETGLAADGAIGERLDRGGVPAMAPHAAITALQRALDHADTVVAVADIQWDRFAYGYTAVRPSPLIGELPEVKRLRETGGPAAGEPGAGPDGSPAEALRKRLAGISRAEQSLVVLEVVRSGAAAALGHSSTDEVGAGRAFKELGFDSLIALELRNRLTAATGQKLPATLVFDYPTPTALAEFLCARIVGDGGTAAAPGVAELDALESALSVLDPDSEARETIAARLRDLAAKWAEPRTADAEAAEGDGGTVTEKLQEATPDEVFAFIDKELGI
>NZ_CP023992.1|WP_099013783.1|3467509_3484858_-|type-I-polyketide-synthase
MSDQDKILDYLKRVTADLHQTRQRLREVESQEPEPIAIVGMSCRFPGGVTSPEELWELVAAGGDAIADFPTDRGWDVESLFADDPDEQGTSYTDKGGFLDGAGEFDAAFFGISPRETLGMDPQQRLLLETSWEAFERAGIDPATLRGSKAGVFVGTNGQDYPELMHTLPQGVEQYLLTGNAASVISGRISYTFGLEGPALTVDTACSASLVALHLAIQSLRNGECSLALTGGVTVMNSPRAFINFSRQRGLAPDGRCKAFADGADGTGWGEGVGMLLVERLSDARRHGHNVLAIVRGSAINQDGASNGLTAPNGPSQQRVIRQALTDARLTPAQVDAVEAHGTGTSLGDPIEAQALLATYGQNRPDGRPLWLGSIKSNFGHTQAAAGVAGIIKMVKAIEHGVLPRTLHVDAPSRDVDWDAGAVSLLTENTPWPETGQPRRAGISSFGVSGTNAHTVIEQAPAEDREPRAAGGDATPSRWSGIGGLVPVLVSAQSAPALRAQAERLTARVQGDPDLGLTDLAHSLATTRAALDQRAVVLAGEGGREELLRGLAELAEDAPAGSVVRGEVAEGKLAFLFTGQGSQRAGMGRELYAAVPAFARALDEVCAELDQHLQRPLREVMFGDDSAQLDRTGHTQPALFALEVALFRLLETWGVKPDFLVGHSIGELAAAHVAGVLSLADAAKLVAARGRLMEELPTGGAMIAIQASEDEVAPLLTERVSIAALNGPTSVVIAGDEDAAVAIAESFRARDRKTKRLTVSHAFHSPRMDGMLDAFREVARQVTYGPPVIPIISNLTGGSVSADEICSPDYWVRHVREAVRFTDGIRRLEEYDVATYVELGPDGVLSAMAQDCVTSDGAVFVPVLRGDRPEATALAGALARAHVHGVAVDWAAVFEGSGAHRVELPTYAFQRELFWPEPPGPWTGDVTAAGLGSADHPLLGAAVSLADGAGFLFTGRLSLQTHPWLADHAVMDTVLLPGTAFVELAIRAGDHVGADVLEELTLEAPLVLPPQGGVQLQVSVGAPDETGRRSLTLHSRLEDAADGTWGEGEWTRHATGVLAGGATTPDENLTAWPPAGATEVPVDGLYDWLAETGFAYGPVFQGLQGAWQHGNQVYAEVRLPESARAEAELFGLHPALLDAALHAVGIGSLLEDTEHGRLPFSWSGVRLHAVGAATLRVRLSPAGQDAVAVLVTDESGAPVASVDSLLLRPVSPDQVHAARGAFHEALFRVEWTPAPVPAATTVVAGQWAVLGAEHPELAAALPTAVGYADLAALGAAVDAGAPLPQAVVAPFFADDTGLPVRAAVRDALHRALELTQNWLADARFEGSRLVIATRGAVATSADADTEDLAHAPLWGLLRSAQSENPDRFVLVDIDGDDASYLALAPALATGESQLAVRTGTVVVPRLAKVASADRTAPALDPEGTALVTGATGTLGGLVARHLVAEHGVRRLLLLSRRGADAHGAAELVAELRESGAEVTLTACDVADRDALAGVLAAIPAEHPLTAVVHTAGVLDDGVIGSLTAERVDRVLPPKVDAAWNLHELTRDNPDLSAFVLFSAAAGTLGGPGQANYAAANAFLDALAHRRHAQGLPATALAWGLWAERSGMTGDLDDTDIQRISRAGVAALSSEEGLALLDTALAVGDPTLVPMHLDLAPLRHADATMVPALLRGLVRAPGRRVVETSGGAAPGGLADRLLGLSVPERDRLLLEIVCGQVAAVLGYAGPEAVGAGRAFKELGFDSLTAVELRNRLGAVTGVRLPATLVFDYPTPTSLAGFLRTEILGDQADEAAAAPAATVAVADDEPIAIVGMSCRYPGGVTSPEELWQLVTGSVDAISGFPTDRGWQLEGLLGDDPEQTGTSATIEGGFLYDAGEFDPDFFGINPREALAMDPHQRLLLETSWEAFERAGIDPATVRGSKTGVFAGVMYHDYLSRLTALPDGLEGYLGTGTAGSVASGRVSYTFGLEGPAVTIDTACSSSLVALHLAAQALRNGECTMALAGGVTVMSTPDTFIDFSRQGGLSASGRCKSFSADADGTGWAEGVGMLLVERLSDAKKNGHKVLAVVRGTAVNQDGASNGLTAPNGPSQQRVIRQALANAGLSASEVDAVEAHGTGTTLGDPIEAQALLATYGREKSEDQPLWLGSIKSNFGHTQAAAGVAGIIKMVQAMHHGVLPRSLHLDEPSPHVDWAAGAISLLSEAREWPQTGRPRRAGISSFGVSGTNAHAIIEQAPESEPAEVSALPAARPSVLPWALSGKNADALRAQAERLLADLERRPELSPTDLAYSLATTRAALDHRAVVVGGDRAALVVGLEALARGESAAGLVQGSVADGKVAFLFTGQGSQRPGMGRELYDAYPVFAEALDAVCDELDAYLERPLKTVMFGDDAQELDQTGFTQPALFAIEVALFRLVEAWGLRPDFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQALPAGGAMIAVQAAEDEVLPLLTDRVSIAALNGPTSVVIAGDEDAALEIAAAFEARGRKTKRLTVSHAFHSPRMDEMLEAFREVAQGLSYEAPRIPIVSNLTGNVVSGEEITSPDFWVRHVREAVRFLDGIRTLAAQGVTTYLELGPDGVLSAMGQDCLAESDADVAGFAATLRKDRDEAETVATALAALHVRGVTPDWSAYFAGTGAHRVDLPTYAFQHRRFWLTSPAGFVGDVESAGLDRADHPLLGAAVPLADSDGFLFTGRLSLESHPWLADHAVMGTVLLPGTAFVELAIRAGDQVGCDRLDELTIEAPLVLPERGAVQLQIVVGAPQQAGHRTLELYSRAQDAPAEMPWIRHASGVLVAGAPRPSFDLTAWPPQGAEPAEVEGLYEHLAQGGFAYGPMFQGLTAAWLRGDEVFAEVRLPEDRKADAATFGLHPALLDAALHSTFARAGGDEQGRLPFSWSGVSLHAVGADALRVRLTPAGADGVSLELADGTGAPVASVEQLALRPVSAGQLAEGRSAAYHESLYRLDWATVPLSTESPAVSWTVLGEGAPAPLTSGAEIHADLDALAAAGDAPAYVLAYLDPRGATGDEVTAAVHTATQRALALVRAWLADDRFAASRLVMVTRGAVATAGDAGTHDLPHAPVWGLVRSAQSENPDRLVLVDLDGTDASYEALGAALASGEPQFVLRRGAVHAPRLARTAASGPMVPPPGEPAWRLDIQDKGTLENLTLLPSPEAAAPLETGQVRVAVRAAGVNFRDVLNALGMYPGDAGLMGSEGAGVVLETGPGVTDLAPGDRVMGMLPGGFGPLVVVDRRMIAPMPEGWSFAQAASVPIVFMTAYYALRDLAGLRGGEALLVHAAAGGVGMAAVQLARHWGVDVYATASQGKWGTLRSLGLADDRIASSRDLAFEEKFREASGGRGVDVVLDSLAREFVDASLRLLPRGGRFVEMGKTDVRAPEEVAAAYPGVSYQAFDLTEAGLDRIQEMLCELLELFRQGALRALPITAWDLRQAPDAFRYLSQARHIGKVVLTVPAPWNPDGTVLITGGTGTLGGLVARHAVTERGARRLVLTSRRGEQAAGAAELAAELRELGAEVTIAACDAADRDALAAVLAGIPAGHPLTAVVHTAGVLDDGVIDSLTPERLEKVLRPKVDAAVNLHELTRDQDLAAFVLFSSAAGTFGGPGQANYAAANSFLDALARHRQAQGLAATSLAWGLWAEASGMTGALEATDKSRMNRSGVLGLSSAEGLALFDAAQEVGDAFLVPMQLDLAPLTGAPIEMVPPLLRGLVRGGTTRRTAESGAAGDGSSLVERLVRLDAAERERTLLDLVRAQVAVVLGHDSPDAVEASRAFKDLGFDSLTAVEFRNRLGAAAGLRLPATLVFDYPSPTALAGYLLEELLGSEAAAAVPARAEGPSGSVTDEDDPIAIIAMSCRFPGDVRTPEDLWELLAEGRDGIARLPEDRGWDLEAFYDPDPDRPGTSYAREGGFYYDAHHFDPAFFGINPREALAMDPQQRLLLETSWESFERAGLDPGALRGKQVGVFVGQMHNDYVSRLHTVPEGVEGYLGTGGSSSIASGRVSYTFGFEGPAVTVDTACSSSLVALHLAAQALRGGECTMALAGGVTIITTPDVFTEFSRQRGLARNGRCKPFAAGADGTAWGEGVGMLLVERLSDARKNGHKVLAVVRGTAVNQDGASNGLTAPNGPSQQRVIRQALANAGLSASEVDAVEAHGTGTTLGDPIEAQALLATYGREKSEDQPLWLGSIKSNFGHTQAAAGVAGIIKMVLAMHHGVLPKSLHIDEPSPHVDWESGAVSLLSEAREWPRTGRPRRAGISSFGMSGTNAHTIIEQAPESEPAEAPALPAARPPVLPWVLSAKTPEALRAQGARLRAHVADHPELPLAGIGHSLAASRVPFEHRATLVAADQDGFLAGLDALAEGRSATGLVEGSVAEGGKLAVLFTGQGSQRLGMGRELYDAYPAFAEALDTVCDALDPHLERPLKTVVFGDDAEELDRTGFTQPALFAIEVALFRLVETWGVRPDFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQRLPAGGAMIAVQASEDEVTPRLGKRVSIAAVNGPTSVVVAGDEDAALEVAAAFEAEGRKTKRLTVSHAFHSPHMDGMLDAFREVAQGLSYEAPRIPIVSNLTGAVVSAEEIATADFWVRHVREAVRFLDGVRILEAQGVTAYVELGPDGVLTAMAQDCVTEDGGSFAAALRGGRPEAETLLTAVGTAHVRGAAVDFTALFAPYGPGLVDLPTYAFQRRSFWLDAGPVGGDATAIGLHAAGHPLLGAAVELPDSDGIAFTGRLSLQTQPWLADHAVMGTVLLPGTAFVELALRAGDHAGCDRLDELTLEAPLIVPDQGAVQLRLSLAAPDDTGRRALTLHSRAEGAPADEPWLRHATGALAAGMVESSFDLSAWPPAEAEKIEVEGLYEGLADSGFAYGPVFQGLTAAWRRDDEVFAEVRLPEDRKSDAGAFGLHPALLDAALHALGLSAAEEGNGQGRLPFSWTGVSLHAVGASALRVRLGGTATGTVTLELADTTGAPVASVEGLALRTISPDQLATPRPGTPSDSLFRLDWTPVPAQSTEVTPNRWAAVGPDTLDLPAYADLDALAEAIASGTRHPEYVVADLANQARPVLEDGAIQARPAIEDTPEGRQASVDGAASEARPVAGNPARPALEDRGPGAEPMAGAANQARPAFEDTPEGRQGSWGLPQVSGRGGIGESSSPAETAHQATTHVLDLLQKWLTDDRFTDSRLVLLTSGAVSTGTDAPATDPAQAAIWGLARSAQAENPDRIVLVDTDRKDDPQQTLATALATGEPQLAVRDGAVKAPRLARATVATDQETPALDPEGTVLVTGASGTLGALFARHLVAERGVRHLLLLSRRGETAPGAVELTTELRELGADPRWAACDAADRKTLAETLAAIPTDHPLTAVVHTAGVLDDGVIASLTPERMATVARPKAHAAWNLHELTQDADLSAFILFSSASGVFGGPGQGNYAAANAFLDALAQHRRANGLPATSLAWGLWSVAGGMGGELDEAEIARIRRGGVGVLTAESGLELFDAAQGSDEPLLVPLPLDMAALRAQAGSGMLPALFRGLVRAPARRAAESAAAAAAGAEALRERLAGLSDPERAEVLLELVCTQVAAVLGYPGPETVDPARSFSEVGFDSLTAVELRNRLNATTGVRLPATLVFDYPTPNALVEYLRGEILPDDASAVTSLLAELDGLEKSLAGATPDDEDRSRITARLQALLAQWNDNRGPEDGAGVAEELESATDDDLFDFIGKEFGIS
>NZ_CP023992.1|WP_099013782.1|3455738_3467447_-|type-I-polyketide-synthase
MNEEKLRYFLKRVTADLHETRRRLQEVESEDQEPIAIVGMSCRYPGGVSSPEDLWRLVSEGGDGISEFPTDRGWDIGRLFDDNPDGAGTSYVREGGFLHDANYFDPAFFGINPREALAMDPQQRLLLETTWEVFERAGIDATSVRGTRTGVFAGVMYHDYASRLRAVPPGVEGYLGTGGSSSIASGRVAYTFGLEGPALTVDTACSSSLVTLHLAMQALRNGECSLALAGGVTVMSTPGTFTEFSRQRGLSFDGRCKSFAASADGTGWSEGAGMLLVERLSDARRNGHKVLAVVRGSAINQDGASNGLTAPNGPSQQRVIRQALASARLTADHIDVVEAHGTGTTLGDPIEAQALLATYGKEKPAERPLLLGSIKSNVGHTQAAAGVAGIIKMVKAIEHGYVPKSLHIDEPSPHIDWSAGAVSLLTEGRPWPETGRPRRAAVSSFGISGTNAHLIIEQPPAEDPEGEEEAAEAPAEGTAATEAPAEEAVAPAEETAAPRTLPLLPWLVSGKGEDALRAQAARLHTYVAERPELDPVSLGYSLATTRAALENRAAVIAADRATFLDRLAALASGEPAAGVVQGVETRGKLAFLFTGQGSQRLGMGRELYDAYPAFAQALDAVCAALDPRLERPLKDVLFGDDTAALDRTGFTQPALFAIEVALFRLVESWGLKPDVVSGHSIGEIAAAHVAGVFSLDHAALLVAARGRLMQRLPGGGAMIAVQASEDEVAPLLTEGVSIAALNGPTSVVIAGDEDAAVAIAASFEAQGRKTKRLTVSHAFHSPLMDPMLEAFRKVAESLTYEAPKIPVVSNLTGTIAPAAEIATAGFWVRHVREAVRFLDGMRAMEAQGVTTYLELGPDGVLSALGQECLAGESEHVALVPVLRSGRPEAETLTTALATLHTRGTAPDWAAYYAGTGAERVELPTYAFQREHYWLDAGTAYGDVSSVGLGSADHPLLGAAVSLADAEGFLFTGRLALDTHPWLADHAVMGAVLLPGTAFVELAVRAGEQAGCDLVEELTLEAPLILPERGGVRLQIAVGAPDDTGRRTLALHSRPDEAGDDEPWVRHATGALAADAAEGSFDLSAWPPAGAERIDTDGLYEGLADAGFGYGPVFQGLRAAWRGDGEVYAEVALPEDTDPGAALFGLHPALLDAVLHTIGLSDLTENPGQGGLPFSWTGVRVHSVGADTVRVRLSPAGNGTVSLQLADVTGAPVASIDRLALRTVSPDQLTAPGGASDALFTVDWTPIPATSEQVSPDRWAVVGPEVPGLGTLGGEIAAYADLGALAEAVAAGTALPERVVVSLTGDSAAPEGPGAAIQARPALEDRGPGRSPGGVQGAEPLVSGRGGIGENPATTAHQTTAQTLTLLQTWLADANFTDTHLVILTDATNLPHSAAHGLIRSAQSENPGRITLVDTDTHPDSLEALPTALASGEQELAVREGTVKAPRLARATTQPETETPEWNPDGTVLLTGASGTLGTLFARHLVTDRGVRHLLLVSRRGETAPGAAELTAELEALGAEAHWSACDVADRDALAATLAAIPAEHPLTAVVHTAGVLDDGVIASLTPERLATVLRPKADAAWNLHELTQDADLSAFILFSSAAGVFGGAGQGNYAAANAFLDALAQHRRANGLPATSLAWGLWAESGGMAGDLDEAELARLRRGGVAAITADQGRELFDLANATDSALLVPMPLDLAALRTQAAAGMLPPLFRGLVRVPPRRAAQAAAAARSGALAQQLAGASADEADAIVLGLVRAQVAAVLGYAGPEAVDPRRAFSEVGFDSLTAVELRNRLTAVSGVRLPATLIFDYPTPAALAEYLRAEAQGGQEDAAAPVAAATAGDDEPIAIVAMSCRFPGGVTSPEDLWKLVAEGADAITDMPTDRGWDIESLYDDDPDQQGTSYARNGGFLHDAHHFDPVFFGISPREALAMDPQQRLLLETTWEAFERAGIDPAAVRGSRTGVYTGVMYNDYGTLLHRAPDGLEGYMGTASSGSVASGRVSYTFGLEGPAVTVDTACSSSLVTLHMAVQALRGGECSLALAGGVTVMATPGTFVAFSKQRGLATDGRCKPFAAAADGTAWGEGVGMLLVERLSDARKNGHPVLAIVRGSAINQDGASNGLTAPNGPSQQRVIRQALANARLSAAEVDVVEAHGTGTTLGDPIEAQALLATYGQEHTEDEPLWLGSVKSNFGHTQAAAGVAGIIKMVKAIEHGVLPRTLHVDEPSPHVDWSAGAVSLLTEQTEWPETGRPRRAAVSSFGISGTNAHTIIEQAPAERPTAAAAPEPGALPWLLSGGSEAALRAQAERLLEHLDADPGLRPADVGYSLATTRAVHDRRAALVGTDREDFTRALTALARGEAAAQLVQGTGTAGKTAFVFPGQGSQWAGMAVGLMDASPVFASRIHECAAALAEFTDWSLVDVLRGADDAPSLERVDVVQPVLFAVMVSLAELWRSLGVRPSAVVGHSQGEIAAACVAGILTLQDAARVVTLRSQAIGRVLAGKGGMVSVALPVAEVRERIEPWGEERISVAAVNGPSSVVVSGEPEALDELVASCEADEVRARRVPVDYASHSAQVELLREELLELLAPVGPKTAEVPFLSTVTGEWVEGPELDAEYWFTNLRRTVELEGAVRRLLDEGFGAFIESSAHPVLTMGVQETAEDAGREAAAIGSLRRDEGGLDRFWTSLGEAWTRGVTVDWEAVYEGTGAVRVELPTYAFQHERYWIEVPLSVGDVASAGLGAAGHPLLGAAVELPDSDGFLLTGRLSLQTHPWLADHAVSGTVLLPGTAFVELAIRAGDQVGCALLEELTLEAPLILPARGGIQLRLTVGAPDASGRRTLEVYSRPEPDAHRGGDASEVPWSRHAGGVLAPGDAADSGEDLSVWPPAEAVALDVDDLYERFAAGGFGYGPAFQGLAAAWRRGEEVFAELRLDQRQHADAALFGLHPALLDAALHGVALGEFLGAGADGIRLPFSWTGVTLHAAGATALRVRIAPAGPDTVALTVADENGGAVASVDSLVLRRIAPEQLRAAQVTYHDSLFRLEWTPVPAPSADPGAVRWALVGEQAAADGTDAFGLVGALESIGAECEVFSDLTELAAVVASGRPRPDVVLLPLTGPAGGGGGHLSEDVRLATHAALDTAQSWLAEEAFAGARLAFVTRSAVATSPDAEVSDLTHSSVWGLIRTAQTENPDRFLLLDLDHEETAADALVGAVAGGEPQLAVRASALHAPRLARVATQGEDRTPEGLPEFDPDGTVLITGATGVLGGQLARHLVAERGVRHLLLNSRRGQRAQGMPELVGELTALGAEVSVAACDVADREALSMLLAEVDPAHPLTAVVHTAGVLDDGLLPALTPERIDTVVRPKADAAVNLHELTLGLDLKAFVLFSSAAGIFGAPGQANYAAANTFLDAFAAHRRSAGLPALSLAWGLWEQRSAMTGGMADADVARMERSGMAPLSSRDGLELFDTACGVGGEAVLVPLHLDTAPLREQAAEGALPAVFRGLVRAPARRRAVSAGAADTGGPSLARRLAGLAEAEREKAVLDLVRGQAAAVLGFADAEAVGAARGFLEQGFDSLTAVELRNRLGAASGLRLPPTLLFDHPTPELAARQLLARLAGAMAAEGGAVSDAAREEAAGAEPSAALGAMLREAGQLGRQEEFTRLLMDLSRFRPSFASAAELDKAPALVRLSRGETGPALVCFSSILSIGGPHQYARFAAGFRGRRDVWAMGNPGFVAGERLPATPEAVVEAQAEAVLRETDGAPFVLLGHSSGGLLAHEVAARLESTGVFPDAVVLLDIYSHDRDAAVGLQPGLSAGMDERSAGQVPVDDTRLLAMGAYFRLFGEWRPSEIKTPTLLVRAGERLFDWSRDDGDWRSYWQLPHTALDVAGNHFTMMEEHAGTTARAVEDWLS
>NZ_CP023992.1|WP_099013781.1|3455453_3455669_+|hypothetical-protein
MAANRPDRDEHPKMTMRVYTMAHNGIVTARRAIVAVLDGEKGDAYSLGQAWPPCQCPRHRDHNNPDRFKRS
>NZ_CP023992.1|WP_142881432.1|3455115_3455454_+|hypothetical-protein
MEVGDPVIADGRATPVLSPGCALCAAPGDFGPHNPTEPRSGLCPACVAAGKPTRDGLEQAVLIVAGQTLAGAEALDLAGATPEELTYHLGAMKRSLRGLLQLLAPVTGEEGR
>NZ_CP023992.1|WP_099013779.1|3454108_3454963_-|helix-turn-helix-domain-containing-protein
MDGERPLNRKELHPDSSPLAAFGARLRSLREGRGWTQEDLAERTGYSSVHVSAIETARKPPTLRLVRSIDRAFGTEGTADSFEREWREIRHGSLLVGFPEYVGHEGRAAEIRLYEVGVIPGLLQTPEYATALAEGAVKRGAITAEQAQERVAFVAERQAALVRTSPPLVFVVLDESCLRRPVGEPAIMNAQLEQLIEFAGRPNTVLQVAPFDMGTRRPFDLPLYILTMSDRSLMSYAESAQRGHFERDSTSVVPLLTAYHQLQAEAPSQAQSVAMIRQLRKGTP
>NZ_CP023992.1|WP_099013778.1|3453902_3454112_-|DUF397-domain-containing-protein
MTTESPRWFKSSYSNNGGACIEVAANLVASRGVVPVRDSKDPHGPALMFEPTAWSSFVSAVRHGEFPIT
>NZ_CP023992.1|WP_099013777.1|3452158_3452626_+|NUDIX-hydrolase
MTYTPPLWPVSVKGVALDAQDRVVLLKNERDEWELPGGRLEIGSPDGAVPPDASPEAALEREIQEETGWEVKAGPLIDGGVWIYQPIPGRRVLIVTYGCTVLTPDRPPVVSHEHKQLGMFTADEVPELTMPDGYKQAIAAWYGRRDVGLDDYERM
>NZ_CP023992.1|WP_099013776.1|3449661_3449826_-|FxLD-family-lantipeptide
MPKAGTSYAAEATSDFDLNIEVLASAPVVPGLLNDTGDGCTATCQSACSNSTCG
>NZ_CP023992.1|WP_099013775.1|3446553_3449592_-|lantibiotic-dehydratase
MYHAVDAVLIRAAAHSLSAELPPWPDLNGNLADDVDRWRKWIEQVCANETTAAAIEFASPLLAEAVNGILSGHSQRPRTVRRAAVSLVRYLLRMRHRATPFGLFAGPAPVRLGDTAEARWRTNHHVTVRADDAWLTAIVTTLETVPGLLWRLPVMADPTRIVRGTSIVISHQPGKDGPVEVTMRRTPAVETVLRLAQSPITVGDIVAKLSADYPDTPSSVIGDMVGGLVANRVLLTSLRAPMTVDDSLGHLVSQLDAIGADADSETAAALRQIHQLLTQHDTAPTGEQPTIRTEATRRMTSLRSVPDRPLVANLRPDCDVTLPSAVAEEAEHALAVIARISPYPAGYPAWQDYRARFLERYSIGALVPVRDLVDPDIGLGFPAGYRGSVLKRPVVATTRRDEYLLALAQEAAVNSAREIVLTEEDCAALTVAGVARVPAHVEMCFTVLADSLDALQSGRFALSLAGLSLGAGRTTGRFLTMLEQPDQDRMRAAYAAMPTLDADAAVAQISSPPLRLRTQNVSRAPAVAPHLLSLGEHNPTGTLDLDDLAVSADTQRLHLVSLSTGRHIEPTVMNAVELTNATHPLVRFLTEVHRSHAAALTPFAWGAATRLPFLPEIRVGRAILSPACWRLRQRDMGNESRPGWIHRFTDWRCRYGVTRTVHLGADDQRLRLDLDNPIHLQLLRSELARADAVTLHEAPDEDALGWLGHAHEITMPFASVLLPSPSTAGTRAVVRRSSGRIPGTSRWAYLKIYCHADRAREILTTHLPALFQEWGDEPPLWWFTRYSDPGTHVRLRLLLPGPYVFGAAAQRVGPWAATLRNDGLISRIQWDTDEPETGRYGTGCALDAAERYFAADSAAAVAQMALNLPVDLRPAVIAASFADIATVFVGNPVAGRCWLIENLLKADGPAPARDLQAQATRMSAPDTNLAALRTLPGGEAVVTAWVDRRVALKAYRTALIDEGAAPATVLPSLLHMHHNRTAGIDPDGEATCRRLARAAALSWTVRAKGALR
>NZ_CP023992.1|WP_099013786.1|3516689_3532442_-|type-I-polyketide-synthase
MANEETLRDYLKLVTADLHQTRLRLQEAEAKNHDPIAIVGIGCRYPGGVQSPEDLWRIVSEGVDAVSEFPLDRGWNVDTMYHPDPDHPGTSYVHEGGFVDGIADFDPSLFGISPREALGMDPQQRMLLETSWEAFERAGIDPVAVRGRQIGVFVGTSNHDYLGAILSSNENFEGYFGTGNAASVASGRLSYTFGFEGPAVTVDTACSSSLVALHLAVQALRNGECSLALAGGATLMCAPGVFVDYSKMRGLALDGRSKPFAPEADGFCLGEGVGMLLVERLSDAQRKGHPVLAVVRGSAVNQDGASNGLTSPNGPSQQRVILQALANARLSPDQVDAVEAHGTGTALGDPIEAQALLATYGQDRPEGKPLLIGSIKSNIGHAQAGAGVGGIIKMVMAMRHGQLPRTLHLTEPTPHVDWTAGDVELLTATREWVKDPEDATPRRAGVSSFGMSGTNVHTILEEAPAPAAPAENGEPEPERTEPPLVPVVLSGKNEQALRAQALRLRTHLAAHPGHRLADIGYSQAVTRAALDRRAAVVAADHDELLAGLDALAEGRHHPEATEGLAAEGKVAFLFTGQGSQRLGMGRELYETYPVFAEALDAVCAQLDRFLDQPLKGVLFGDDAATLDRTGFTQPALFAVEVALFRLVESWGLRPDFLAGHSIGELTAAHVAGVLSLTHACALVAARSQLMQQLPTGGAMIAVQASEDEVAPLLTERVSIAALNGPTSVVIAGDEDAAVAIAESFQAQGRKTKRLTVSHAFHSPHMDGMLENFRQVAERLTYEAPKIPIVSNLTGTLVSADEITTPDFWVRHVREAVRFLDGVRRLEDHGVTTFVELGPDGVLSAMAQECVTGDKNRTFAFLPALRSGRPEARTLGQALAQAHVRGVPVDWSRYYAGTGARRVELPTYAFQRQRYWPANPFSYGIDSAAAEAAAPALSDARFWEVVHSEDLPALVETLGLDGDQPLSEVLPVLSAWRRRSHVDTTVDSWRYRVTWTPLPQTPDKPLTGTWLVAAPEGRDDDPWVAEPLRLLAERGVSVHRIDVDGTTVDRAALAERIRAALSPDPAAGADTARPDGVLSLLGLDERPHDQHPSLTAGLAGTLALVQALGDAEVDAPLWAATRGAVSVGRSDRLTSPEQAQLWGLGRTAALEHPERWGGLIDLPATADDRALGRLADILAGPEGISGEDHLAIRPQGIHARRLARAPHHETTGDGWTTHGTALITGGTGALGGHVARWLVAHGAQHILLVGRRGPDAPGAAGLRDDITALGAQVTIAACDVADRDALAGLLATVPADLPLTTVVHAAGVLDDGVLDAQTPRRMADVLRAKADAARHLDELTRGLDLSAFVLFSSMAATFGAAGQANYVAANAYLDALAERRRADGLPATSMAWGAWADGGMATDELVAERLRQSGLPALAPEPATAALGAALDLDETFSLVVDIEWDRFAPGLSGHRPNSLLAELSEARHAIEAARTATGGPAIPGRSTTLAQRLTDAGTDEERDQIALDFVRTQVAVVLGHPGPDSVEPSRAFRDLGFDSLTAVEIRNLLSTLTGLKLPATIIFDYPTPIALADHLQAELIGSRPAVTGASSVGVALDDDPIAIVGMSCRFPGGVRSPEELWRLLASGQDAVVDFPADRGWDLETLYDPEGTGEHTSYVREGGFLADAAEFDPVFFGISPREALAMDPQQRMLLETSWEAFERAGIDPTTLRGQQVGVFAGTNGQDYLPVILSAPDGSEGFMGTGNAASVMSGRVSYALGLEGPAVTVDTACSSSLVALHWAIQALRAGECSLALAGGVTVMSTPGSFVDFSRQRGLAADGRIKAFAAGADGTGWGEGVGMLLVERLSDARRNGHEVLAVVRGSAINQDGASNGLTAPNGPSQQRVIRQALAGAGLSPSEVDAVEAHGTGTKLGDPIEAQALLATYGRDRDADQPLWLGSIKSNFGHTQAAAGVAGVMKMVLAIQHGLLPQTLNVDEPTPHVDWSAGAVALLTEAREWPETGRPRRAAVSSFGISGTNAHTIIEQAPGYADEAEDAAPDAAPRSGVPATWVLSAKSPEGLRDQAARLRAHLDERPELDATDVAFTLATRRTAFEERAALVAEDRDGLLSGLAALAEGRTAAGLVRGSVSGGKVAFLFTGQGSQRLGMGRELYDAFPAFADALDEVCAHLDAHVERPLRDVLFGEDAEALDRTGFTQPALFAIEVALFRLVEAWGLKADFLSGHSIGELAAAHVAGVLSLADACTLVAARGRLMQELPAGGAMIAVQASEDEVAPLLTERVSIAALNGPTSVVIAGDEDAALEIAAGFESQGRKTKRLTVSHAFHSPRMDGMLDTFREVAEGLSYEAPRIPIVSNLTGTVVSAEEITTADFWVRHVREAVRFLDGVRTLEAQGVTTYIELGPDGVLTAMAQECVDAESDAAFAAALRKDRPEAEALLSAVARAQVRGVAVDWAAYYAGTGATQVVLPTYAFQRQRYWPKVSSLFLGDVAAVGLGEAEHPLLGASAELPDADGMLFTGRLALSTHPWLAGHTILDTVLLPGTAFVELAIRAGDHVGCDYLEELTLEAPLVLPAQGGVQLRLSVGAADGTGRRPLSLHSRPESLPAEEPWTRHATGVLSSGGRPEASFELSAWPPVDATEVELDGRYEGLLDIGFAYGPAFQGLRRAWQRGGEVFAEVALDEGTAEEAAAFGLHPALLDSALHAIGMGGLGNTGGEGRLPFAWTGVSLYASGASALRVRLTPAGNDGVRLEIADTTGAPVAAVETLGLRPVSAEQLQSARTAYHESLFRLEWTTTAGLADAAGADVPTDGRWAVLGADPFGLGTTAYGDLATLAAAVSAGTAPAPEYVVVSPSAELGEQSARAAHRAAAAALTAVQRWLEEERFGDAPLVVVTHGAVAAEADEPVADLAGAAVWGLLRSAQSENPGRFVLVDTDGREESLRALPAALASDEPQLAIRAGAVSVPRLARVAVEPEGDDARGLDPEGTVLVTGASGSLGGLVARHLVAERGVRHLLLVSRRGEQAPGAAELAAELVGLGAEVAWAACDVADRGALAATLATVPAEHPLTAVVHTAGVLDDGVIGSLTPERVDHVMRPKVDAAWNLHELTRDLDLTDFVLFSSSSGVFGGPGQGNYAASNAFLDALARHRSAQGLPATALAWGLWAGAGMGSTLDEADISRMRRAGLPPLPVAEGLALLDTALTVREASLVPMRVDLAALRNQPAISPLFRGLVRIPARRAVDAVAAGGETGLAGRLAGLSEPEQERLLLDLVRAQVATVLGYAGAETIGSGRAFKELGFDSLTAVELRNQLNTVTGLRLPATLIFDYPDPQVLARHLRTELVGTDSPAAHTPVPVVAVTDDEPIAIVAMSCRYPGGVTTPEELWQLLAAGEDGISRFPDNRGWDLEALYDPDPETQGTSYAREGGFLHDAADFDPAFFGISPREALAMDPQQRLLLETTWEAFERAGIDPLSVRGSRTGVFAGVMYHDYGSRLHAVPNEVEGYLGTGSSSSVVSGRVAYTFGLEGPAVTVDTACSSSLVALHLAAQALRQGECSLALAGGVTVMFTPGTFIDFSRQRGLARDGRCKSFAAAADGTGWGEGAGMLLLERLSDAKKNGHEVLAIVRGSAVNQDGASNGLTAPNGPSQQRVIRQALANARLTTGEVDVVEAHGTGTTLGDPIEAQALLATYGRERDAERPLWLGSVKSNLGHTQAASGVAGIIKMVLAMRHGLLPQTLHVDEPSPHVDWSAGAVSLLTEAREWPETGRPRRAAVSSFGISGTNAHAIIEQPPALEPGEPAVEPEALPYVPVLVSARTEDGVRAQARRLRSRIAAEPRTALTDLGFSLATTRAALEHRVALVAEGHDGADEVLGALDALARGEHPAQALRGVATEGKVAFLFTGQGSQRLGMGRELYGAFPRFAEALDEVCDELDRHLERPLKTVLFGEDAQALDRTAVTQPALFAVEVALFRLVEAWGLTPDYLAGHSIGEIAAAHVAGVFSLADACALVAARGRLMQELPGGGAMFAVQASEDEVAPLLTERVSIAALNGPMSVVIAGDEDAAAGIAAGFEAQGRKTKRLTVSHAFHSPHMDPMLADFRKLAEGLTFNAPKIPLVSCLTGTVAAADEIRLPEFWVRHVRESVRFLDGVRTLRDQGVTTFVELGPDGVLSAMGEDCLAETETETGTDGNTDARAVFVPTLRGGRSEAQALATALAQIHVRGAAPDWAAVYAGRGARRVELPTYAFQRQRYWLDVGISVEDVISAGLGTADHPLLGAAVELPDTGGFVFTGRLSLLTHPWLADHAVMDTVLLPGTAFVELALRAGHEAGCDTVEELTLQAPLVLPEQGAVQLRLELAAADESGRRPLTLHSRREDVPADEPWIRHATGFLAPSATSASSATSTPSASSATSTPSASGEQTVERVDLSVWPPADATALATDVFYEGAAAAGLGYGPVFQGLDAAWRRGDELFAEIRLPQGFEPQAAAYGVHPALLDAALHTLGLDPEGEGSEGARLPFAWTGVRLYAEGAASLRVRLRPGAEGVSLHLADGTGAAVATVDGLVLRPLSAEQLSASRAAYHESLFRPEWTALPGSATDIPLGERWVTLGAATGFTVAGERLDDHADLAALTTALDGGAPAPDVVVVPLTGVASFTATGGGESLTATDGAALLPATDGAAPLTATGGSASIADTARAAARNALDLVQNWLNDQRLADTRLVLVTRGAVAAAPGEDIADLVHTTVWGLVKSAQSENPGRFVLVDTDGTDASQRALPSVLATDEPQLALRSGTGHAYRLARVPALPDTPEPAGLGDPDGTVLLSGATGALGGLFARHLVAERGARRLLLVSRRGGEAPGAAELAAELGELGAEVTWAACDTADRDALAATLSAIPAEHPLTAVVHTAGVLDDGVISSLTGERIDTVLRPKVDAAWNLHELTRDLDLAAFVLFSSAAGAFGSSGQGNYAAANTFLDALAQHRHAQGLPASSLAWGLWAAADGMAGSLDASDVTRISRGGFEALGQDAGLALFDLAGTLSEAVLVPIRIDTGALRGQAAAGLLPPLLRGLVRTPVRRSADTGATGAGAVADSGAGSLAERLSGLSETERDRELLDVVRGHVAAVLGYATPDDVDAGRGFLDLGFDSLTAVDLRNRLGAAAGLRLPVTLIFDYPTPTALAGYLREELGLEGAAGHPPVHAELDKLEAILATIAPDDIERPGITTRLRDLLSKWNETQSATDSTAEDREIQSATADEIFDLLDDELGLS
>NZ_CP023992.1|WP_099013787.1|3532706_3537701_-|type-I-polyketide-synthase
MATANEAKLREYLKKVTTDLTAAHRRLQEVDDQAHEPIAIVGMSCRFPGGVSSPEELWQLMVSGGEAQTEFPADRGWDLQNLFDPDPDTPDTTYTREGGFLDDATRFDAAFFGISPREATAMDPQQRLLLEASWEAFERAGIDPASLRGSRTGVFAGMNASDYLTVAIDAQDDFGGHLGTGNASSVVSGRLSYVFGLEGPAVTVDTACSASLVALHLAVQSLRLGECSLALAGGVHVMSTPGLFIEFSRQRGLSEDGRCKAFSADADGFGPAEGVGVLLLERLSEARRNGHKVLAVVRGSAVNQDGASNGLTAPNGPSQQRVIQQALAGARLSGNDVDVVEAHGTGTSLGDPIEAQALLATYGQDRTEEQPLLLGSVKSNIGHTQGAAGIAGVMKMVLAMEHGVVPESLHIAEPSPHIDWSSGKIALVRSATPWPETGRPRRAGISSFGFSGTNAHTILEQAPAEEPGPVELVSKQPGVLPWVLSGKSEAALRAQAWRLLDRLHDEPALRPVDIGLSLATTRAALDHRGVVQGRDREELMAGLTALAEGGMAAGVERGSVVAGQTAFVFPGQGSQWVRMGVGLMDASPVFAARIEECAGALGEFTDWSLVDVLRGAEGAPSLERVDVVQPVLFAVMVSLAELWRSLGVVPAAVIGHSQGEIAAACVAGALSLKDAARVVALRSQAIGRVLAGKGGMVSVALPVAEVRERIAPWGEERISVAAVNGPSSVVVSGEPTALDELLASCEADEVRARRVPVDYASHSAQVELLREELLELLAPVQPKNAQVPFLSTVTGEWIDGPELDAEYWFTNLRRTVELEGAVRRLLDEGFGVFIESSAHPVLTMGVQETAEDAGVDAAAIGSLRRDEGGLDRFWASVGEAWSRGVNVDWDAVFDGTGARRVELPTYAFQQQRYWPEPAPARAAGEIGHDAVEAKFWAAVEAEDWQALAAELTVEGDQPMSAVLPALASWRKQAREQSAVDGWRYRVTWKPLAEERSPRLSGAWLVVVPGAPATENTDTWTDAVAGVLAERGADVRRIAVDTGVDGREELAERLRAALADADGTPFAGVVSLLAPAEGAHPEHPSLPAGTAAQLALIQALGDAGIGAPLWCLTRGAVSVGGSDRPASPEQALVWGLGRVAALEHLERWGGLIDLPETSDERALTRLVGLLASDGDEDQAAIRAAGVFGPRLVRAPLADTSTVRSWKPTGTTLVTGGTGRLGAQVARWLARNGADHLVLASRRGPEAPGAVELEAELTGLGAKVTLAACDVTDRAALAETLAAIPADQPLTAVVHTAAVIEDGVIEGLTTDQAERVLRLKVDATRHLHELTRDLDLTAFVLCSHFSATFGAPGQGNQAPGNAFLHAFAEQRRADGLPATALTFGPWGDGGTVDGAVGDRMRRHGINEMAPEPATATLQHALDRDETALTVIDMDWRRFTLAFTADRARPLLHDLPEAREVVEEMAAAETEGTGAAAGAALAGQLAALPETERERVLLDLVRSAVAAVLGHSGAQAIEAGRAFKELGFDSLTAVELRNRLGAASGLKLPPSLIFDHPTPAAVAAYLRAGIAPDEAADGTAVLDELDKLETALTGTAPDNITRARITMRLQSLLAKWNESDGTAVTAEPAAAAAAPERPAKDTVDAEQLQSASDEELFAFINKGLGRA
>NZ_CP023992.1|WP_099013788.1|3537766_3563566_-|type-I-polyketide-synthase
MTTPNEKLVDALRASLKETERLRKQNQQLTDASREPIAIVGMSCRFPGGVGSPEELWRLVADGQDAISGFPTDRGWDIESLYDPDPEREGTFYARGGGFLYDASRFDPGFFGISPREALAMDPQQRLLLETSWEAFERAGIDPASARGSRTGVFVGASTQAYGAGEYDLPEGVEGHLLTGTASSVASGRLSYAFGLEGPAATIDTACSSSSVALHLAVQALRQSECSLALAAGATVLSSPDVFVEFSRQRGLSADGRCKSFAASADGTGWSEGVAVLLVERLSDARRNGHPVLAIVRGSAVNQDGASNGLTAPNGPSQRRVIRQALENARLTPADVDAVEAHGTGTTLGDPIEAQALISTYGQERPEGRPLWLGSLKSNIGHTQNVAGIGGVIKMVMAMRHGVLPRTLHVDEPTPHVDWSAGEVSLLTEARPWPETGGPRRAGVSSFGVSGTNVHTIIEQAPESEPAETSVAPAVTPAVLPWVLSGRGAAALRAQAERLVAHVEAHDELRPVDVGYALATSRAAFEHRAVMVAEDRAGLLTGLGALARDESAPGLVEGSVAGGKVAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCAELDAHLERPLRDVLFGSDAEALDRTGFTQPALFAVEVALFRLVEAWGLKADFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMIAVQASEDEVAPLLTERVSIAALNGPTSVVIAGDEDAAVAIAAGFEAQGRKTKRLTVSHAFHSPRMDGMLDAFREVAQGLSYEAPRIPIVSNLTGGVVSAEEITTADFWVRHVREAVRFLDGIRTLEAQNVSTFIELGPDGVLTAMAQDCVTGEDAGFISALRKDRPEAEALTTAVARAHVRGVAPDWAAYFAGTGAHGVDLPTYAFQRERFWLEPGAASVGDVASVGLELAGHPLLGAAVPLAESDGLVFTGRLGLDTHPWLAEHTVRDAVVVPGSAFVELAVRAGDQVGCDLLDELTLHAPLVLPARGGVRLQVTVGAPDGDGRRSFTVSSRAEDAAADTVWLRNAGGVLASGAPGPSFDLAQWPPTAAEAIEAEALYARLAEAGLRYGPLFQGVMAAWRRGDELFAEVRLDDDAKPGAEEFAVHPALLDAALHALHGREGARLTDVWQGVSLYAEGASALRVRIAPAGADTVSVALADATGEPVAAVDALRCRPLPDDLAGDADVVRRSLFQLDWVAPQTSSAGPDAATRRIVLGDDPFGLVTAGVAATSAPDLAALGASVEAGETAAPELVLASFAPVPSTPVSGGSDEGVAEAAHRAARRALALVQGWLADERFGDARLVIVTRGAMAADAEEGVTDLVHAPLWGLVRSAETENPGRFVLVDVAEAAEAAEAAGAAEAAGGVGAAEAAGTAGAAEVPGTFADALSDALATGEPELALRAGRPLAPRLTRATAPAAGSGSAPAAGSAAALGSTPTSDSAAAPNANSRPDATAFDADGTVLITGGTGALGRLLARHLVAEHGVRHLLLTSRRGADADGATELAAELRERGAEITLAACDAADRDALAATLAAIPAEHPLTAVVHTAGVLDDATAAALTPEQLERVLRPKVDAAWNLHELTRDLDLSAFVLFSAIAGTLGGAGQANYAAANVFLDALAAHRHAAGLPATSLVWGLWAQSGGITGDLTETDLLRLARSGMGALGDDEGMALFDAARRTGRTLLIPARLDLAALRSAAGSGPVPALLRGLIRTTGRRTAAGALGAGSSLAQRLRALSPNERRRTLLELVRGHVATALGHASADAIEARRAFKELGFDSLTAVELRNRLSAATGLKLPSTIVFDHPNPTVLADHLRAELLGPDIDGAGAEAEQADPALPATTASLADDPIAIVAMGCRYPGDVRSPEDLWQLVATGSDAITGFPVNRNWESQWAADGDEAPSEYARAGGFLHDADLFDAAFFGISPREALAMDPQQRLLLETSWEVFERAGIDPDALRGRSVGVFVGAAYSGYDAGLEQAGAEVAGHVMTGNAGSVMSGRIAYALGLEGPAVTVDTACSSSLVALHWAIQALRQGECTMALAGGVTVMTTPGHFAEFGRQGGLAADGRCKAFAAGADGTGWGEGVGMLLVERLSDARRNGHQVLAVVRGSAVNQDGASNGLTAPNGPSQQRVIRKALASAGLTSGDVDAVEAHGTGTTLGDPIEAQALLATYGQERDAERPLWLGSIKSNIGHAQAAAGVAGIIKMVMAMRHGVLPRTLHVDQPSPHVDWTTGDIALLTERVEWPETGRARRAAVSSFGISGTNAHTIIEQAPATTAEPAVAEAGRDGAGVLPYALSAKGADALRAQAERLYAHLTARPDLEPADVAHTLATGRAALDHRAVLVADGRGDLLRGLDALARGESAPGLVEGTVAEGETAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCDELDAHLERPLKTVVFGDDAEALDRTGFTQPALFAIEVALFRLVEAWGLKADYLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMIAVQASEDEVLPLLTDRVSIAALNGPTSVVIAGDEDAALEIAASFEAQGRKTKRLTVSHAFHSPRMDGMLDTFREVAEGLTYDAPRIPIVSNLTGAVVSAEEVTTADFWVRHVREAVRFLDGVRTLEAQGVTTYIELGPDGVLTAMAQECVTGGNAAFAAALRKDRPEAEALTTAVARAYVRGVAPDWAAYFAGTGAHRVDLPTYAFQHRRYWPEEPVASLAAAGVDGWRYQVAWKPLSLGSAARLSGVWLVVTPAGEAAADVWAHGVVRTLTERGAEVRRLDLADGDRAAIAERLRTAADGGAVAGVLSLLATGDDADALLPTAALVQAMGDAAIDAPLWCATRGAVSTGRPGELVDPARAQVWGLGRVAALELPDRWGGLIDLPETMTDRVLSRLAVVLAGAGDEDQIAVRASGVFGRRLARATARQVAESEGWRAHGTVLVTGGTGALGGQVARWLIDRGAGHVVLAGRRGLDAPGAAELRDELAASGARITVAACDVADREALAGLLADLPAEFPLTAVVHAAGVLDDGVLESLTPERFASVLHAKADAALALDELTRDLDLSAFVLFSSTSGTVGAAGQGNYAAANAFLDALAERRHAQGLPATSIAWGPWAAGGMAADEALEQRMRRAGMPPMDADLAIDALQRALDLGDAAVTVADVEWDRFAAGFTAGRPSPLLADLPEVRQAAARSAATAGEAAVVETASALARRLLGLPEAERHRALLDLVRTHVAEVLGHADVSDISAERAFREIGFDSLTAVELRNGLNAATDLRLPATLIYDYPTPLALADHLFAELLGGQAVATGGASPVAGAADGDDPIAIVAMSCRFPGGVRTPEELWRLLVSGTDVISDMPADRGWDLRTLYNPDPDVEGTSYVREGGFLHDAADFDPAFFGISPREALAMDPQQRLLLETSWEAFERAGIDPATLRGSTAGVFVGTNGQDYLSLLLGDSQGLEGHMGTGNAASVISGRLAYTFGLEGPAVTIDTACSSSLVALHSAIQALRGGECSIALAGGVTVMSTPGVFVDFSRQRGLAEDGRIKAFAAEADGTGWGEGVGMLLVERLSDARRNGHPVLALVRGTAVNQDGASNGLTAPNGPSQQRVIRQALAGAGLAPSEVDAVEAHGTGTRLGDPIEAQALLATYGRDRAEGQPLLLGSIKSNIGHTQAAAGVAGIMKMVLAMRHGVLPRTLHVDQPTPHVDWSAGDIELLTEAREWPETGHPRRAGISSFGFSGTNAHAVLEEAPAADTVEAADEGGAALPVLLSARTADGLRAQAEQLHGHLTARADLRPADLGYALAVGRSAFEERAALVAEDRDGLLSGLVALAEGRQAAGLVQGSVAGGRVAFLFTGQGSQRLGMGRELYYAYPAFAEALDAVCDELDAHLERPLKTVVFGEDAEALDRTGFTQPALFAVEVALFRLVEAWGLRPDFLSGHSIGELAAAHVAGVLSLADACRLVAARGRLMQELPAGGAMVAVQASEDEVAPLLGERVSIAALNGPTSVVIAGDEDAAVEIAASFEAQGRKTKRLTVSHAFHSPRMDGMLDAFREVAEGLTYEAPRIPIVSNLTGGVVSAEEITTADFWVRHVREAVRFLDGIRTLEARNVTTFIELGPDGVLTAMAQECVTDAASDAAFVSVLRKDRPEAEALTTAVARAHVRGVAVDWAAFYAGTGAVRLAPDELAELPTYAFQRQRYWPKVSSLFLGDVAAVGLGEAEHPLLGASAELPSADGMLFTGRLALSTHPWLADHTIMDTVLLPGTAFVELAVRAGDQVGCELLEELTLEAPLVLSQDGGVQLRLWVGAADDTGRRPLELHSRAEHLSAEEPWTRHASGVLASAGAPEASFELSAWPPADAAEVEIGDRYAELRDVGFAYGPAFQGLRRAWRRGGEVFAEVALDEGTAEEADAFGLHPALLDAALHALGLAGLGGTENEGRLPFAWTGVSLYASGAATLRVRMAAVGGDGVRLEIADATGAPVAAVDSLVLRPVSAKRLQSARTAYHESLYRVEWTTAGPVDAAVDAQWAVLGTDAYGLGATAYADLAALGEAVDSGAALPEYVVVPLANQARPGPFSDGAVLEGPGAANQACPAIEDTPEGRPGVHADGAVLEGPGAANQACPAIEDTPEGRPHPHADGAALEGPGAASPARPALEDRGLGAEPQVGGRGGIGENPTQAAHDATTQALHLLQTWLADDRFTDSRLVLLTSGAVATEAGEPVTDLAGAAVRGLLRSAQSENPDRLLLIDVDGDDSQAALPALPALSAALASGEAEVAVRQGVLKTPRLARAASAAESEPPEWNPDGTVLVTGASGSLGGLFARHLVAERGVKHLLLVSRRGDQAAGAAELTAELAELGATVSWSACDVADRDALAATLATVPAEHPLTAVVHTAGVLDDGVIGSLTPERVDHVMRPKVDAAWNLHELTRDLDLSAFLLFSSAAGVFGGPGQGNYAAANVFLDALAQHRAAQGLPATALAWGLWAGGGMGDTLDEADITRMRRAGVPPLPVAEGLRLFDAALTVDEASLVPMRLDLAALRNQPASSPLLRGLVRGPARRAVDAVAAGGETGLAGRLAGLSTAEQERLLLDLVRAQVATVLGYAGAETIGSGRAFKELGFDSLTAVELRNQLNTVTGLRLPATLIFDYPDPQVLARYLRTELVGEESAEVHTPVPVAAVTEDEPIAIVGMSCRYPGGVTTPEELWQLVIGATDAVSEFPVDRGWDLDALYSDDPDQVGTSYTREGGFLHDAADFDSDFFGINPREAMAMDPQQRLLLETSWEAFERAGIDPAAVRGSRTGVFAGVMYHDYLTRLTAVPEGLEGYLGTGGAGSIASGRVAYTFGLEGPAVTIDTACSSSLVALHLAAQALRNGECSMALAGGVTVMATPDTFIDFSRQQGLSTDGRCKSFAASADGTGWAEGAGMLLVERLSDARRNGHRVLAVVRGSAINQDGASNGLTAPNGPSQQRVIREALTSARLTTADVDVVEAHGTGTTLGDPIEAQALLATYGRNRPEGQPLWLGSLKSNIGHTQAASGVAGIIKMIMAMRHGVLPQTLHIDEPTPHVDWSAGDIELLTEARPWPELGRPRRAAISSFGVSGTNAHTIIEQLPAAEEIPATGPAAELPTVPWVLSGKSEAAVRGQAERLLTHLGTHPELNTMDIGYSLATGRAALERRAVVIGEDRDGLLSGLAALARGESAAGLVQGTAAEGKVAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCDELDAHLERPLKTVLFGEDAEALDRTGFTQPALFAIEVALFRLVAAWGLRADFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMVAVQASEDEVLPLLGERVSIAALNGPTSVVIAGDEDEAVAIATSFEAQGRKTKRLTVSHAFHSPRMDGMLDAFREVAEGLSYEAPRIPIVSNLTGTVVSAEEITAADFWVRHVREAVRFLDGVRTLEAQGVTTYVELGPDGVLTAMAQECVTGDAAAFVSALRKGRTEPGALTAALAALHTRGLALDWSAYFAGTGARGVELPTYAFQRQRFWVENPEEVREAVAAMDSVDARFWEAVEREDLEALAGTLQSEDADADALSSLGAVLPMLSSWRRRQGERSTVDAWRYQVTWKPVAARAEGTLTGRWLVVAPADASAGGAYGVLAEGVVRTLSARGAEVQLVEPTAEDRTGLAELLREAVADAPVAGVFRLPSLTEGADGLLRTAALAQALGDVGVDAPLWVATRGAVSTGRADGPVDPWQARVWGLGRVAALELAERWGGLVDLPETVDDRALSRLVGVLAGGAGEDQVAVRASGVFGRRLTRAAETAATTERGRDWRPGAGSVLVTGGTGALGGHVARWLIDKGAEHVVLTSRRGLDAPGAAELRDELAASGARVTVAACDAADREALAALVAGLPAELPLTAVVHAAGVLDDGVLESLTPERFASVLRAKADAAANLHELTRDLDLTAFVLFSSFAGSIGAAGQANYAAANAFLDALAERRRADGLPATSVAWGPWAEGGMAADDALEQRMRRAGVPPMAADLAIAALQRALDLDETAVTVADIDWERLAPGFTASRPSPLLLELPEVRTALEAEGLRTATNGGGADESSLVQRLAGVPATERERMLLDLVRSAVADVLGHSDAEAVEADRAFRDLGFDSLTAVELRNRLNTVTGLRLPPTLVYDYPSSSALAAHLRTEILGDESAGTGAEAAAGVPSTTAAVADDPIAIVGMSCRFPGGVRSPEELWRLLVSGQDAVTGFPADRGWDLEALYDPDSATDNTTYVREGGFLADVGDFDAAFFGISPREALAMDPQQRMLLETSWEAFERAGIDPTTLRGQQVGVFTGTNGQDYMSLVLHSPDGGDGFMGTGNAASVMSGRVSYALGLEGPAVTVDTACSSSLVALHWAIQALRAGECSLALAGGVTVMSTPGSFVDFSRQRGLAADGRIKAFAAGADGTGWGEGVGMLLVERLSDARRHGHEVLAVVRGSAINQDGASNGLTAPNGPSQQRVIRQALAGAGLSPSEVDALEAHGTGTTLGDPIEAQALLATYGQDRPEGRPLWLGSIKSNIGHTQAAAGVAGVMKMVLALRHGVLPPTLHVDEPTPHVDWSAGELELLTEAREWPETGRPRRAAVSAFGISGTNAHTLLEQAPEPEESPATAPAVELPTVPWVLSGKSPAAVRGQAERLLAHLGGGTAPAATDVAYSLATTRAALDHRAVLTADSGDGLLAGLAALARGESEVPGLVEGSVSSGKVAFLFTGQGSQRLGMGRELYDAFPAFADALDEVCAHLDAHLERPLRDVLFGEDAEALDRTGFTQPALFAVEVALFRLVEAWGLKADFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMIAVQASEDEVAPLLTERVSIAALNGPTSVVVAGDEDEAVAIATSFEAQGRKTKRLTVSHAFHSPRMDGMLEAFREVAEGLTYDAPLIPIVSNLTGEVVSAEEITTADFWVRHVREAVRFLDGVRTLEARGVTTFVELGPDGVLTAMAQDCLAEPEAAELLPALRKGRPEAEALTGALARLYVRGPAPDWAAFFAGTGARKVALPTYAFQRSRYWVDAQLSLDEVASAGLGSADHPLLGAAVELPDADAYVFSGRLSLASHTWLADHTVADTAVLPGSAFVELAVRAGDHVGCALLEELTLDEPLILPERGGVRLRVSVSEPDGDGRRPLAVYSRDERSDTDRPWTRHAAGVLGSAEAPAGGGAEPLAVWPPADAEAVDTDELYASMARAGLLHGPAFQSLGRVWRRGEEVFAEVRIAPERQPEAARFALHPALLDGALQPLALGADGAAVARSWRGVKLYAVGAEALRVRLALTEDGAVSMLAADETGALVASVDALVTGALEVDRIAGATASDRHESLFRIDWAPVAAPSEAASAGIAVIGGDELKLSVALETAGFRATVHDDLGSLNAAIEAGGPVPDTVLVPFPPEPGAAEGGLAAGAHTATHRVLGLLQEWLNGGRPGAARLVVVTRGAVAAAGDPAVTDLVNAPVWGLLRSAQTENPDQFVLLDVDGEVSYPAIAAALGSGEPELALRAGAAYAPRLARVEAAPVITKAIDTPEAAKAIDATGSAGQAIDPDGTVLITGATGGLGRLFARHLATAYGARHLLLTSRSGPAADGMAELVAELAELGARATVVACDAADREALAGLLAGIPADRPLTAVVHTAGVLDDGVIDMLTPERVDTVLRPKVDAAVNLHELTRDLDLSAFVLFSAAAGTLGGAGQGGYAAANVFLDALAGHRRATGRTAQSLVWGMWAEERGMGGRLGEADQQRAARGGVLPLAAEEGLALFDAAHAVADEPVLVPVRLEMATLRAAAATGGLLPLYRGLVRTPVRRAATGGPAAPEAVAEAGEGTLAQRLAGQSEAQQQRTLLDLVRRQVAGVLGYASKDQVGAEQAFKELGFDSLTAVELRNRLNAATGLKLTATLVYDYPTPVALARHLRQEVAPEADGPGVSVLEELERLENSLSSLTSEDLESVMEDEAAHANIAVRLQTLLAKWNDVRRTADDAGAEAEAEAFEEVSDDELFDFIDKRFGNG
>NZ_CP023992.1|WP_167460018.1|3563591_3573926_-|SDR-family-NAD(P)-dependent-oxidoreductase
MTTELRRTRRRLTEVEADAQEPIAITAMSCRFPGGVGSPEDLWQLVAEGGDAISGFPADRGWDIEGLADPDPDRKGTFYNSGGGFLDGVAEFDPGFFGISPREALAMDPQQRLLLETSWEAFERAGIDPTSVKGSRTGVYVGAAAMGYGSDVQGAPQELEGLLLTGGATSVLSGRIAYTFGLEGPAATIDTACSSSLVALHWATQALRQRECSLALVGGVTVMPNPDVFVEFSRQRGLAPDGRCKSFAASADGTGWSEGVGVLLVERLSDARKNGHPVLAVVRGSAVNQDGASNGLTAPNGPSQRRVIRQALENARLSAAEIDVVEAHGTGTTLGDPIEAQALLATYGQERPEGRPLWLGSLKSNLGHAQAAAGVAGIIKMVMAIRHGVLPKTLHVDQPSPTVDWTAGEVSLLTEARPWDETGRPRRAGVSAFGVSGTNAHTILEQAPAPEDFPAPDGDTTPAANAAKVTAAVLPWTLSARNAAALRDNARRLASHLDREPALSTADVGHSLATGRAALERRAVIVGEDRAGLTAALEALARGESAPGLVEGTVAEGETAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCAELDAHLERPLRDVLFGEDAEALDRTGFTQPALFAVEVALFRLVEAWGLKADYLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMIAVQAAEDEVLPLLTERVSIAALNGPTSVVIAGDEDAALEIAAGFEARGRKTKRLTVSHAFHSPRMDGMLDAFREVARGLSYEAPKIPIVSNLTGGVVSAEEITSPDFWVRHVREAVRFLDGVRTLEAKGVTTFIELGPDGVLTAMAQECVTGEDAGFIAALRKDRPEAEALTTAVARAHVRGVAVDWAAYFAGTGANRVDLPTYAFQHERFWLEPGAASVGDVASVGLELAGHPLLGATVPLAESDGLVFTGRLGLDTHPWLADHVVRDAVVLPGTAFVELAVRAGDQVGCDLLDELTLHAPLVLPAHGGIRLQLTVGAPDGAGRRSLTVLSRAEDAPAEEPWTRHADGVLASGAPRPSFALTAWPPQGAEAARTEELYAALADGGLRYGPVFRGLTAAWRRGDELFAEVRLDESIASEAQAYGLHPALLDSALHALGLGDGDDQGRLPFAWSGVALYASGASALRVRLVLRGADGVRLEIADSAGAPVAAVDSLVLRAVSAEQVRAARAAYHESLFRVEWIELPAGVGAGASGGGRWAVLGTDAFGLGATAYADLAELGEAVDSGMALPEYVVVCPALERPGAAIQARPALEDRGPGRSPGGVQGAEPLHAAEPHIDAAGRGRVGESPSLATTAHQATTQVLGLLHQWLADERFATSRLVFMTLGEGEPVRDPAQSAVWGLLRTAQAENPDRFVLLDIDGQDTSLAALPAALAAGEEQLAVRAGVVRIPRLARVPVAEEAGMAADFGAAGTVLVTGASGSLGGLVARHLVAERGVRHLLLVSRRGERAPGAVELAAELTELGAEVAWAACDVADRGALAATLATVPAEHPLTAVVHTAGVLDDGVIGSLTPERVDHVMRPKVDAAWNLHELTRDLDLTAFVLFSSASGVFGTPGQGNYAAANAFLDALAAHRRAEGRPAVSLAWGPWAGAGMAGGLDEADISRMRRAGLPPLSPAEGLALLDTALTTDEVAPVPMRVDAVALRAQAAAGALAPLLRGLVRVPVRRAVDAAAGGGSALAERLAGLSEAERDRLLLDLVRTQVAAVLGYAGPQAVEEGRAFKDLGFDSLTAVELRNLLREATGLRLPPTLVFDYPTSTALAGHLREEIVGDTAAAIVPDRVLSAVDREDPIAIVAMSCRFPGGVRSPEELWQLLLAGEDAITPFPADRGWDLATLYSDDPDREGTSYTREGGFLHDVADFDASFFGISPREALAMDPQQRLLMETSWEAFERAGIDPATLRGTSTGVYIGSNDRDYLTLWLNEPQGLEGHLGTGNSSSVASGRLSYAFGLEGPAVTIDTACSSSVVALHLAAQALRGGECSLALAGGVSVMSTPGAFLEFSRQRGLAADGRIKAFSGDADGTNWAEGAGVFLVERLSDARRNGHPVLAVLRSTAINQDGASNGLTAPNGPSQQRVIRQALANAGLSPADIDVVEAHGTGTALGDPIEAQALLATYGQDRPEGRPLWLGSAKSNIGHTQAAAGAAAIMKMVMAMRHGVLPRTLHVSEPTPHVDWSAGDIELLTEARPWPETGRPRRAGVSSFGFSGTNSHAIIEQAPAANAVSAPAPERSLPVLAWPVSARTEDALRAQAARLRPSVDADAGAGTPRPLDLAYSLATSRAALEHRAVLLGRDGDLLGEQLAALAEGRGATGLVEGSVAGGKLAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCAELDAHVERPLREVLFGEDAEALDRTGFTQPALFAVEVALFRLVEAWGLKADFLSGHSIGELAAAHVAGVLSLADACTLVAARGRLMQELPAGGAMIAVQASEDEVAPLLTERVSIAALNGPNSVVIAGDEDEALAIAAGFEAQGRKTKRLTVSHAFHSPRMDGMLEAFREVAEGLTYEAPRIPIVSNLTGTVVRAEEITTPDFWVRHVREAVRFLDGVRTLEAQGVTTYVELGPDGVLTAMAQECVTDADAAGFAAALRKDRAEAETVTAALAQAYVRGAEVNWAGYFAGTGAHRVDLPTYAFQRRRYWPDALETGARAEGAVDTVDARFWEAVESEDWESLATELRVEGDQPLSAVLPALSSWRRAQRERSAADGHLYNVVWKPRPQGPSGSPAPSGTWLTVVPASHADDPRIAAVADDLTRRGARVVRVELDAADTDPATVADRLAAATADGPVAGVLSLLALDERPHPEHPAVPVGLALTGALAEALARRGDDAPARLWCATRGAVSTGGADRLDSATQAQVWGYGRVVALEQPERWGGLIDLPETVDERALDRLAAVLAGSGDEDQVAIRATGVFVRRLAPAPRTAATSAAEPWTPRGTVLVTGGTGALGRHVARWLARNGAERVVLLSRRGPDAPGAAEIVAELSGTDTAVSVEACDVADRDALAVLVEKLAVGGTPVRAVVHSAGISQEPGTGTELPEFARIVAAKTTGAVHLDALFGEDADPLDAFVLFSSIAGVWGSGGQGAYAAGNAFLDALAEQRRARGLTATSVAWGPWAEGGMAAEGDAEEQLRRRGLPPMAPELNMVAFQRVLSREETAVTVADVDWERFAPAFTAARPRPLIDDVPQVATVLRGGDEGESADTAAKDGASALRERLAGLSGADREDAVLEVVRSHVASALGHASADEVEARRAFNELGFDSLTAVELRTRLGAATGLKLPASLVYDYPTPAALAEHLLTELIPDGPGHGPGHGHGYTPAYADTDPQDAELRRTLATIPMSRIREAGLLDTLLRLADPQATTSDPSRVEDDAESIDEMDVQHLIDMALDLDSLDGNES
>NZ_CP023992.1|WP_099013790.1|3574018_3598642_-|type-I-polyketide-synthase
MVSESVDFTPEHTEMGDASPRGASPWRDRLAALPEAERAEALTAWVGEIVEQALKDKAPDVLDPERPFLDLGFDSLATVDLHARLTAATGLRLPVTLAFDHPTPADLARHVRTELLGGNDDSDVSPADAGMGPIAADEPIAIVGMSCRFPGAVGSPEELWEIVAGGKDVISEFPGTRGWDLAGLYDPDPDRPGSSYTREGGFLHDADEFDPAFFGISPREALAMDPQQRLLMETSWEVFERAGIDPAILRGGRTGVFVGAETQDYGPRLHEAEQGFEGYLVTGNAASVASGRIAYTFGFEGPTVTVDTACSSSLVALHLAVQALRSGECTMALAGGAAVMANPGSFIAFSRQRGLAADGRCKPFAAAADGTAWGEGVGMLLVERLSDAQRNGHRILAVVRGTAINQDGASNGLTAPSGPAQQRVIRQALANAGLTAGEVDAVEAHGTGTTLGDPIEAQALLATYGQNREADRPLWLGSLKSNIGHTQSAAGVGGIIKMVMAMRHGVLPRSLHIDEPTPHVDWTGGDVELLTEARPWPESDRPRRAGVSSFGMSGTNAHAIIEQPPAPAEERADAEDPDDEAAAAPALLPWTLSAKTTDALRGQAERLYALLEADPGLALTDIGHSLATTRATFEQRAVLLAGDRDGFRSALRTLADGGDAPSVVRGAPAAGKLALLFTGQGSQRLGMGRELYGAYPVFAEALDDACWYLEEQLERPLLDVLFAEEGTPEADLLDRTDYTQPALFAVEVALYRLLESWGLRPELLAGHSIGELAAAHVAGVLSLEDAAALVAARGRLMQELPAGGAMIAVQASEDEVAPLLTERVSIAALNGPTSVVIAGDEGVALEIAASFEAQGRKTKRLTVSHAFHSPLMDGMLAEFRRVAQVLDYAPPRIPVVSTVTGRVATAEELCSPEYWVRHVREAVRFLDGVRTLADKGATTFLELGPDAVLTAMAQDCLPDAEGTAYAPALRGGRPEDETLTAALALAYVRGKKADWAAPYAATNARPIDLPTYAFQRQRYWLNAPAPAGSAAEAAPGSAVDGRFWDVVERGDVAALAAELAVDPGVSLGEVLPALSLWRRQESVRSAVDGWRYRVLWRPVTDRLSAAGVLGGSWVVVVPSGEAGGVWAGGVVRLLAGRGVDVRVVESDAVDRAGLADELRTAVVGGSVAGVFSLLAVGGESGLLRTAALTQALGDVGVGAPLWVATRGAVSVGRSDGVVDPGQASVWGLGRVAALELPERWGGLVDLPETADERALGRLAGVLAGASGEDQVAVRASGVFGRRLVRAATPGSATGAASDGSWTPGAGSVLVTGGTGALGAQLARWLVECGAEHLVLTSRRGLEAPGAVELRDELAASGARVTVAACDVADRDALAELLGGIPAELPLTAVVHAAGVLDDGVLDSLTPERFASVLRAKADAARHLDELTRDLDLSAFVLFSSITGSVGAAGQGNYAAANAYLDALAELRRAEGLPATSIAWGPWAEGGMAGDDAMERRMRREGMPPMVPESALAALRQALELDDTAVTVADIDWEHYTGTLTAVRPSPLIAELAAEAGQRAATGADTAKVVTDADAATPLGERLSGLPKAEQDRALLELVRAQVASVLGHGGTDAVEAGRAFKELGFDSLAAIELRNRLNAATGLRLSATLIYDYPNATALADHLRTELLGADVAVDGGVVAPSAVAVADDPIAIVAMSCRFPGGVRSPEELWELLTAGGDAVAEFPSDRGWDLAGLYDPDPDRQGTTYTREGGFLYDAGDFDASFFGISPREALAMDPQQRLLLETSWEAFERAGIDPATLRGSRTGVFAGTNGQDYAGLVATPPEGLEGHLGTGNAASVVSGRLSYTFGLEGPAVTVDTACSSSLVALHMAVQSLRSGECTMALAGGVTVMSTPDAFVDFSRQRGLAEDGRIKAFAAGADGTGWGEGVGMLLVERLSDAEKNGHPVLAVVRGSAINQDGASNGLTAPNGPSQQRVIRQALAGAGLSAGDVDAVEAHGTGTTLGDPIEAQALLATYGRERDADQPLWLGSIKSNIGHTQAAAGVAGIIKMVLAMRHGVLPRTLHVDEPSPHVDWSTGAVSLLTEQVEWPETGRPRRVGVSSFGLSGTNAHTIIEQAPALPAASAEEPEPREPAVLPWLLSAKDGQALHAQAAQLATHLRTHPELSATDIAFSLATSRAALERRAALVTTDREAFLAGLDALARGESVPDVVEGTAAEGKVAFLFTGQGSQRLGMGRELYDAYPVFADALDEVCAHLDLYLERPLRDVLFGEDAAVLDQTAFTQPALFAVEVALFRLVEAWGLTPDFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMVAVQASEDEVAPLLTERVSIAALNGPTAVVIAGDEDVALEIAASFEAQGRKTKRLTVSHAFHSPRMDGMLDAFREVAEGLTYEAPRIPIVSNLTGGVVSAEELTSPEFWVRHVREAVRFLDGVRTLEAQGVTTFVELGPDGVLSAMAQECVTGDGAAFAAALRKGRAEAESVTAALALPHVRGQAPDWREYFEGTGARRVELPTYAFQRTRYWWEEAPAAETALGGAVDGRFWDVVERGDVAALAAELAVDPGVSLGEVLPALSLWRRQESVRSAVDGWRYRVLWRPVTDRLSAGVLGGSWVVVVPSGEAGGVWAGGVVRLLAGRGVDVRVVESDAVDRAGLADELRTAVAGGSVAGVFSLLAVGGESGVLRTAALAQALGDVGVGARLWVATRGAVSVGRSDGVVDPGQASVWGLGRVAALELPERWGGLVDLPESVDERVLGRLAGVLAGAGGEDQVAVRASGVFGRRLTEASGARTSGDEDWRASGSVLVTGGTGALGAQLARWLVECGAEHLVLTSRRGLDAPGAVELRDELAASGARVTVAACDVADRDALAELLASIPAEFPLTAVVHAAGVLDDGLVDTLDAERLERVVRAKATSARNLHELTRDLDLTAFVLFSSFAGSVGAAGQGNYAAANAYLDALAELRRAEGLPATSIAWGPWAEGGMAADEALERRMRRDGVPPMAPESALAALRQALELDDTAVTVADIDWDRFLAEFTAARPSALFGEVRAARPAPAVEGVPRPAATGGTGTLAERLSGLTENERAQTLLELVRAQVASVLGHGGADAVGAGRAFKELGFDSLTAVELRNRLNAATGLRLPATLIYDYPNATALADHLRTELLGADAAVTGGVAAPTVAVADDPIAIVAMSCRFPGGVRSPEELWELLTAGGDAVAEFPSDRGWDLAGLYDPDPDRQGTTYTREGGFLYDVADFDASFFGISPREALAMDPQQRLLLETSWEAFERAGIDPDALRGQQVGVFAGTNGQDYLSLLMQAPEGLEGHLGTGNAASVVSGRLSYTFGLEGPAVTVDTACSSSLVALHLAVQALRQGECTMALAGGVTVMSTPENFIDFSRQRGLAADGRIKAFAAGADGTGWGEGVGMLLVERLSDARRNGHPVLALVRGSAINQDGASNGLTAPNGPSQQRVIRQALTSAGLTTGDVDVVEAHGTGTTLGDPIEAQALLATYGRERDADQPLWLGSIKSNIGHTQAAAGVAGIIKMVLAMRHGVLPRTLHVDAPSPHVDWSTGAVSLLTEQVEWPETGRPRRAGISSFGISGTNAHTIVEQAPAVDTPAEAPERNGLGGLLPFVLSAKNAEALREQAARLRTHIAARPESAPLDIAHALATGRAALERRAVLTVGDRDELLRSLDALARGESVPSVVEGTVAEGKVAFLFTGQGSQRLGMGRELYDAYPVFADALDEVCAHLDLYLERPLRDVLFGEDTEALDRTGFTQPALFAVEVALFRLVEAWGLKADFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQELPAGGAMVAVQASEDEVSPLLTERVSIAALNGPNSVVIAGDEDDAVAIAAGFEAQGRKTKRLTVSHAFHSPRMDGMLEAFREVAEGLTYEAPRIPIVSNLTGAVVSAEEIATADFWVRHVREAVRFLDGVRTLEAQGVTTYLELGPDGVLSAMAQECVTGEDTAFAAALRKDRPEAEALMTALARAHVRGVTPDWAAVFAGTGAAPVDPADLPTYAFQRQRYWPSAAALAAGDPESIGLGDIDHPLLGAAVALADADGLLLTGVLSLRTHPWLADHAVMDTVLLPGTAFVELAGAAGAQVGCERLDELTLEAPLVLPEHTGVRVQLVVDGPDESGRRSFSLHSRRQDALGTEPWTRHATGVLAPGTRISGEPDELAVWPPRGATPIPVEGLYEELAGAGLGYGPVFQGLKGAWRLGENLYAEVGFPEDAPLTSGAEAERFGLHPALLDAALHIIGLDSADREAALAEGALLPFAWNGVQLHAAGAGALRVRLSERSANAVSLLVADGTGRAVATVESVALRAASADQVRAARGGLHESLFRLDWTAVPAPATGAATGDWAVLGADGAQLAVLEGAFGTGIRLAAYRDLAVLRTAVEAGAPAPDTVLLAGIGGGGDASAVHEATQAVLSLLQEWLADERFTASRLVLLTRGAVATEPGADVADLPYAAVRGLFRSAQSENPGRLVLLDVDAQEDSYRTVPAALGVDEAELALRAGVALAPRLARVPLTESTGGTENTRGTENTGGTEAIDGAGNTDGTESLDGAENTHRTENTDAVGTRAESGAPSYDPNGTVLITGATGNLGGLFARHLVSAHGVRRLLLVSRRGAEADGAEELGAELTAAGATVTWAACDVADRDALAATLAAIPAEHPLTAVVHTAGVLDDGILGSLTPERVTHVMRPKVDAALNLHELTRDQELSAFVLFSGAAAVFGAPGQASYAAANSFLEALAQHRVAQGLPATALAWGLWAGAGMGSGLDEVDLRRIARGGVAPIAADEGLALFDAARADGAPVLFPMRLDHAGLRTEATATGTVPALFRGLVRTPVRRAAAVAATADGSSLAQRLAGLARSEQDRELLELVCGRVAAVLGYAGPEAVEAGRAFKELGFDSLTAVELRNDLKTVTGLRLPATLVFDYPTPSALAGHLREELLGAEEEVAAPLVPVRAGATPAVDDDPIVIVGMSCRYPGGVRTPEELWELVATGGDGISGFPVDRGWDLDGLYHPDPDHTGTSYTREGGFLHDAADFDPDFFGISPREALAMDPQQRLLLETSWEAFERAGIDPSTVRGSRTGVFAGVMYHDYVTGLDGIPDGVEGYIGTGNAGSIASGRVAYTFGLEGPAVTVDTACSSSLVALHWAIQALRAGECTMALAGGVAVMATPETFIDFSRQRGLATDGRCKSFAASADGTGWGEGAGMLLVERLSDARKNGHPVLAVVRGSAINQDGASNGLTAPNGPSQQRVIRQALAAAGLSAGEVDVVEAHGTGTTLGDPIEAQALLATYGRERDADQPLWLGSIKSNIGHTQAAAGVAGIIKMVLAMRHGVLPQTLHVDEPSPNVEWEDGAVSLLTERMEWPDTGRPRRAGVSSFGISGTNAHTIIEQPPAAEDHDGAVARPSAVPPVLPWPLSAVGQDALRDQARRLRDRLRSADEDTDLAAIGYTLAAGRAAFEDRAVLVADGREGFLRTLEALASGEPANGLVQGSPVAGKLAFLFTGQGSQRLGMGRELYDAYPVFAEALDAVCDELDVHLERPLKTVVFADDSAALDRTGFTQPALFAVEVALFRLVEAWGLRPDFLSGHSIGELAAAHVAGVLSLADAAKLVAARGRLMQALPAGGAMVAVQASEDEVAPLLTERVSIAALNGPTSVVIAGDEDAALEIAASFEARGRKTKQLAVSHAFHSPRMDGMLDAFREVAQGLSYEAPRIPIVSNLTGTIVSPDEIATPDFWVRHVREAVRFLDGVRALEAQGVTTYLELGPDGVLSALAQECVTGGDAAFAAALRKDRPEAETVTTALAALHVRGVALDWEAFYGGTAVRRVELPTYAFQRRRYWLDVRSAATATPGATAQDAVDARFWEAVEREDLASLAETLNLGTESNGALEALLPSLSSWRRQQSERSTVDGWRYRVSWKPVTDRATASPSGGWLVVVPAEAAEDAWVEGAVRMLNDRGADVHRVELPAGDDRAALAERLAAAIGDKAVTGGVLSLLALADGDGEGLPRTAALTQALGDMGVGAPLWVATRGAVAVGRSDGMVSPAQARLWGLGRVAALEVPERWGGLVDLPAAADERALGRLAEVLAGAGGEDQVAVRASGVFGRRLVRASGPGSDGGSWTPGAGTTLVTGGTGALGAQVARWLVANGAGHVLLTSRRGLDAPGAVELRDELAASGARVTVAACDVADRDALARLLDAIPAELPLTGVVHTAGVLDDGVLDSLTPERFTAVLRAKAVAAAHLDELTRDRELSAFVLFSSTSGTFGAPGQGNYAAANAYVDALAERRRAEGLPATSIAWGPWAEGGMATDGALEQRLRRGGLPPMDAELAIGALQRALDLDDTVVTVADIDWDRFAPDFTAARPSRLLADLPEIRAAAEDTAAEPAADGSSLAARLAGLGEAERDRLLLDLVRTQVAAVLGHDGSESIGADRAFGELGFDSLTAVELRNRLGAASGVQLPATLVFDYPTASALAGYLRGELIGTDTGASADTAAESTRSTAVTTAADDDPIAIVAMSCRFPGGVRSPEELWQLLTAGGDAIAEFPADRGWDLDALYDPDPDHRGTFYAREGGFLYDAGHFDAGFFGISPREALAMDPQQRLLLETSWEAFERAGIDPATLRGTSAGVFVGSNGQDYDASLHTVPEGVEGYLGTGNAASVVSGRLAYTFGLEGPAVTVDTACSSSLVALHWAIQALRQGECSLALAGGVTVMSSPGAYIEFSRQRGLAADGRCKAFAAGADGTGWGEGVGMLLVERLSDARENGHPVLAIVRGSAINQDGASNGLTAPNGPAQQRVIRQALAGAGLTTGDVDAVEAHGTGTRLGDPIEAQALLATYGRDRDAERPLWLGAIKSNIGHTQAASGVAGVIKMVLAMRHGVLPRTLHVDEPSPHVDWSTGAVSLLTEQVEWPETGRPRRAGVSSFGFSGTNAHTVLEQAPAHDEPAESTPRRPLMRPDVVAWPLSAKGEDALRAQAERLRAHVEAEAGLDAVDVAYSLATTRSALEHRAVVLGPDRDRLLAGLTALARGESAAQLIRGVPAEGRTAVLFTGQGSQRLGMGRELYEASPVFAEALDAVCAELDRHLERPLYDVLFGDDKAPLDRTGFTQPALFAVEVALFRLAEAAGLRPDLLAGHSIGELAAAHVAGVLSLEDAAALVAARGRLMQELPAGGAMIAVQAAEDEVEPLLTDRVGIAALNGPTSVVIAGDEDAALEVAASFEARGRKTKRLAVSHAFHSPLMDGMLAEFRKVAEGLRYGAPRIPIVSTVTGQPVTDELGMAADYWVRHVRHAVRFLDGVRTLEAQGVTTYVELGPDGVLSAMAQDCVTAGAEGAEEVAFVPVLRAGRPEPETLTGALATLHVRGAALDWAALFAGTGAHRVDLPTYAFQRRRYWLEGTPRHTSGEEAAAVDTAGARFWEAVESDDLASLSDAVGIDVDQPLSALLPALSAWRRREREQSALDGRRYRVTWKPLEEPRLAAAPGVWLVAEPAAAAGHAEAVRRVLDALADRGADIRRLTPADGTADGADLDRDALADRIRRAAAEEPVHGVLSLLALDERAHPDHPAVPTGLLRTGVLVQALGDAGLDAPLWCATTGAVSTAASEPVGSAAQAQIWGLGRVVALEHPERWGGLLDLPATLDERAADRLAGVLGGHGDGHEDQLAIRTAGILARRIAHAESTPATGAPWRPRGTVLVTGGTGALGAHVARWLVDNGAEQVVLTSRRGPDAPGADQLTAELTEKGAQVTVVTCDVTDRDAVAGLLTRIRDAHPHHPLTAVVHTAGAGQFAPLAETTPADVADVVAAKVAGAAHLDALLGDTELDAFVLFSSIAGVWGSGGQGAYAAGNAFLDALAEQRRARGLTATSVAWGPWADGGLVADDEAAEQLRRRGLPVMAPHSAIAALQQALDRNETAVAVADVDWGRFAPAFTAARPRPLIADLPEVRAALAPDPAEGADGGTAEAPAESLRQRLAGLTGPEAERALLDLVRTEVAAVLGHDDTTAVQAGRAFKELGFDSLTAVELRNRLNAATGLQLTATLVFDHPTPGVLAGVLRADLLGEDTTPELPALAEIDKLEFALSHVSDDATERERVTARLEALLRTWNETGNAAGADGADDDELDLDAASAEDIFDIINNEFGRS
>NZ_CP023992.1|WP_069864140.1|3598941_3600486_-|PH-domain-containing-protein
MRSETTVRPSSHAAGDWGRLNGRLLLVNLSILAAPVAMFLATLAISGGKTNLQVIITLGSLFVTFLVISGIGLMRLFTTRYRLTEERFELHTGLLFRSERSIQIGRIRGVDLTANPVHRIFGLTTLRIDSGDQSDAAARRLALDGITKAEALELRSRIIALRDAGQSRPVADSDGVLSRLDWSWLRYGPLTVWGVGGVFIAVASTYRTLSELQVDPLELGVIKDLENRFGTIPLWYGILLAAVVIVVLGMIGSTATFIENWAGYELRREDGGILRIRRGLLATRSVSIEERHLRGLELVEPVPLRWAKGAKLNAVASGLGNQEDNRRRRGMTPPTPRGEALRVAAEALPVGPGLIERKGLLPHPKAALRRRINRALIWSVLIAAVPVGLGLWLGSWLVVTGVITGVVLVPVLVAFAMGAYRSLGHGLRGRFLVACSGAFARRTVALERDGIIGWKLSRTPFQRRVGLITLGATTAAGEGVYHVHDLTEGQGIALAETAVPGLLAPFIERAPDRG
>NZ_CP023992.1|WP_079257701.1|3600482_3600992_-|PH-domain-containing-protein
MEAVERHDNLRLRPPRHRVDRRAIGWWTVQSAVFALPLPLVFGILWASIPPTREFFMWATLISLVPGLLYMAVMPAWRYRVHRWEATDEAVYAASGWLWQQWRVVPLSRVQTVDTLRGPIQQMFGLSGITVTTASAAGAVKIKGIDHKLAGDLVEYLAKCTQAVPGDAT
>NZ_CP023992.1|WP_069864134.1|3601061_3601628_-|hypothetical-protein
MPQMSQFMSALIASGTILIIILATDIGRRRITTMRMVRSVIAVAIVIAIFVESFPTKGNDLSLQLVGVGTGVICGLIAGVLLPAYKDATSGELYTIGGIGYALVWIVLSGGRILFAYGAEHWFTMDLIKFSIDYKISGQDTYANAFVFMSLAMVLTRTAVLLAKMRKLKGQDAGSGQLPQQTATGASV
>NZ_CP023992.1|WP_079152983.1|3601795_3603040_+|sensor-histidine-kinase
MRNHSPGEGSQTGAYYGPESGTRWFGLWDGFFAVSYLVTAILLFLSSGSQVSHSIPIAALTLTVPWYAAVGRTLMIEDTYGPRNLVFAAGLVALFCVTTAFNLIGAFALFAVIPMLIMSLPMGWAVVLATVANLCPVLVVAFIGEDLGLSVLGVLPISLLSIALSVLLGLWIKRVVRQSKGRGQLIEELRRSRERVARLSHEAGISAERERLAREIHDTLAQGLTSIISLVQAAESEVREAPDQAVHHLSLAGRVAKESLAEARDFVAALTPPALRGGSLSQAVRRQAEGLIAETGLEVRCSVMGEEKSLPMAVSVVLLRTVQEAIANVRKHAKQARTVDVIVVFDQGGVRLLVRDDGEGFTPDGTQEGYGLRGMQARVAEIDGVASVTSSPGRGTTVEVSVPMTALTGEAVSG
>NZ_CP023992.1|WP_079152982.1|3603032_3603692_+|response-regulator-transcription-factor
MAEGTPGGPSGPGSPIRVLLADDHPVVREGLSAMLDSAEGITVVGQAGSGEEAVVQAVALRPDITLLDLRMGGMDGVEATGQILRQVPGCKVVIVTTYEDDSDILRAVEAGAAGYLLKGSSRQELIDAVQTAARGETVLTPSLAGKLFRSRAPEPSPLSGREREVLRLVGRGLTNAEIGAELFVSEATIKTHLLRSYRKLGVSDRTAAVLKAMEHGLLT

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Crispr_ID: NZ_CP023992_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_7

4051794-4051942

Orphan

Consensus_repeat	Method
TCCCCCACCCCGCCCCTTCCCGAAACCAGGGGCACGCCCCCGGGCCCCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_7

>merge|NZ_CP023992|7|4051794-4051942|CRISPRCasFinder
TCCCCCACCCCGCCCCTTCCCGAAACCAGGGGCACGCCCCCGGGCCCCCACCGGGGCTCCGCCCCAGACCCCGTTCACGGGTGTGGGGCGGGTGGGTTTCTCCCCCACCCCGCCCCTTCCCGAAACCGGGGGCACGCCCCCGGGCCCCC

>NZ_CP023992|7|7|4051794-4051942|CRISPRCasFinder
TCCCCCACCCCGCCCCTTCCCGAAACCAGGGGCACGCCCCCGGGCCCCC	ACCGGGGCTCCGCCCCAGACCCCGTTCACGGGTGTGGGGCGGGTGGGTTTC
TCCCCCACCCCGCCCCTTCCCGAAACCGGGGGCACGCCCCCGGGCCCCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_099013973.1\|4036020_4036233_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013982.1\|4053573_4054770_-\|mannose-6-phosphate-isomerase,-class-I	unknown	unknown	gnl\|CDD\|185085
NZ_CP023992.1\|WP_099013975.1\|4036950_4038156_+\|tyrosine-type-recombinase/integrase	unknown	unknown	gnl\|CDD\|271189
NZ_CP023992.1\|WP_099013979.1\|4046855_4047473_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099013985.1\|4061422_4062985_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069871081.1\|4058250_4059867_-\|L-lactate-permease	unknown	unknown	gnl\|CDD\|224535
NZ_CP023992.1\|WP_099013981.1\|4052532_4053468_-\|cation-diffusion-facilitator-family-transporter	unknown	unknown	gnl\|CDD\|223131
NZ_CP023992.1\|WP_099013977.1\|4039531_4040797_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373673
NZ_CP023992.1\|WP_059149235.1\|4056289_4056472_-\|Trm112-family-protein	unknown	unknown	gnl\|CDD\|225391
NZ_CP023992.1\|WP_099013986.1\|4062981_4067046_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|224137
NZ_CP023992.1\|WP_099013983.1\|4054905_4056210_-\|mannose-6-phosphate-isomerase	unknown	unknown	gnl\|CDD\|378434
NZ_CP023992.1\|WP_069871094.1\|4047606_4049064_-\|adenosylhomocysteinase	unknown	unknown	gnl\|CDD\|377487
NZ_CP023992.1\|WP_069871076.1\|4060873_4061293_+\|metallopeptidase-family-protein	unknown	unknown	gnl\|CDD\|240574
NZ_CP023992.1\|WP_069871078.1\|4060082_4060532_-\|DUF3499-domain-containing-protein	unknown	unknown	gnl\|CDD\|378788
NZ_CP023992.1\|WP_099013974.1\|4036621_4036951_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP023992.1\|WP_099013976.1\|4038224_4039382_-\|S-methyl-5-thioribose-1-phosphate-isomerase	unknown	unknown	gnl\|CDD\|273112
NZ_CP023992.1\|WP_099013972.1\|4034519_4035998_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|226967
NZ_CP023992.1\|WP_099013980.1\|4049473_4051753_+\|PTS-transporter-subunit-EIIA	unknown	unknown	gnl\|CDD\|224218
NZ_CP023992.1\|WP_099013971.1\|4033677_4034517_+\|bifunctional-DNA-primase/polymerase	unknown	unknown	gnl\|CDD\|214927
NZ_CP023992.1\|WP_099013984.1\|4056735_4058094_-\|phosphomannomutase/phosphoglucomutase	unknown	unknown	gnl\|CDD\|236557

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_099013982.1\|4053573_4054770_-\|mannose-6-phosphate-isomerase,-class-I	gnl\|CDD\|185085	PRK15131, PRK15131, mannose-6-phosphate isomerase; Provisional.	1.61401e-115
NZ_CP023992.1\|WP_099013975.1\|4036950_4038156_+\|tyrosine-type-recombinase/integrase	gnl\|CDD\|271189	cd01189, INT_ICEBs1_C_like, C-terminal catalytic domain of integrases from bacterial phages and conjugate transposons. This family of tyrosine based site-specific integrases is has origins in bacterial phages and conjugate transposons. One member is the integrase from Bacillus subtilis conjugative transposon ICEBs1. ICEBs1 can be excised and transfered to various recipients in response to DNA damage or high concentrations of potential mating partners. The family belongs to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	3.93526e-22
NZ_CP023992.1\|WP_099013971.1\|4033677_4034517_+\|bifunctional-DNA-primase/polymerase	gnl\|CDD\|214927	smart00943, Prim-Pol, Bifunctional DNA primase/polymerase, N-terminal. Members of this family adopt a structure consisting of a core of antiparallel beta sheets. They are found in various bacterial hypothetical proteins, and have been shown to harbour both primase and polymerase activities.	8.33578e-17
NZ_CP023992.1\|WP_069871081.1\|4058250_4059867_-\|L-lactate-permease	gnl\|CDD\|224535	COG1620, LldP, L-lactate permease [Energy production and conversion].	1.1187e-135
NZ_CP023992.1\|WP_099013977.1\|4039531_4040797_+\|hypothetical-protein	gnl\|CDD\|373673	pfam15240, Pro-rich, Proline-rich. This family includes several eukaryotic proline-rich proteins.	0.000377651
NZ_CP023992.1\|WP_099013981.1\|4052532_4053468_-\|cation-diffusion-facilitator-family-transporter	gnl\|CDD\|223131	COG0053, MMT1, Predicted Co/Zn/Cd cation transporters [Inorganic ion transport and metabolism].	1.222e-38
NZ_CP023992.1\|WP_059149235.1\|4056289_4056472_-\|Trm112-family-protein	gnl\|CDD\|225391	COG2835, COG2835, Uncharacterized conserved protein [Function unknown].	7.22608e-14
NZ_CP023992.1\|WP_099013986.1\|4062981_4067046_-\|glycosyltransferase	gnl\|CDD\|224137	COG1216, COG1216, Predicted glycosyltransferases [General function prediction only].	1.10267e-28
NZ_CP023992.1\|WP_099013983.1\|4054905_4056210_-\|mannose-6-phosphate-isomerase	gnl\|CDD\|378434	pfam10432, bact-PGI_C, Bacterial phospho-glucose isomerase C-terminal SIS domain. This is the C-terminal SIS domain of a bacterial phospho-glucose isomerase EC:5.3.1.9 protein which is similar to eukaryote homologs to the extent that the sequence includes the cluster of threonines and serines that forms the sugar phosphate-binding site in conventional PGI. This domain contributes a good proportion of the active catalytic site residues. This PGI uses the same catalytic mechanisms for both glucose ring-opening and isomerisation for the interconversion of glucose 6-phosphate to fructose 6-phosphate. It is associated with family SIS, pfam01380.	4.20316e-11
NZ_CP023992.1\|WP_069871094.1\|4047606_4049064_-\|adenosylhomocysteinase	gnl\|CDD\|377487	pfam05221, AdoHcyase, S-adenosyl-L-homocysteine hydrolase.	0
NZ_CP023992.1\|WP_069871076.1\|4060873_4061293_+\|metallopeptidase-family-protein	gnl\|CDD\|240574	cd12954, MMP_TTHA0227_like_1, Minimal MMP-like domain found in a group of hypothetical proteins from alphaproteobacteria and actinobacteria. The subfamily includes some uncharacterized bacterial proteins which show high sequence similarity with Thermus thermophilus hypothetical protein TTHA0227. However, they do not contain the conserved HExxH (x could be any amino acid) motif. They may not have any zinc metallo-peptidase activity.	4.53908e-29
NZ_CP023992.1\|WP_069871078.1\|4060082_4060532_-\|DUF3499-domain-containing-protein	gnl\|CDD\|378788	pfam12005, DUF3499, Protein of unknown function (DUF3499). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 125 to 163 amino acids in length.	1.59574e-57
NZ_CP023992.1\|WP_099013974.1\|4036621_4036951_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	5.50785e-12
NZ_CP023992.1\|WP_099013976.1\|4038224_4039382_-\|S-methyl-5-thioribose-1-phosphate-isomerase	gnl\|CDD\|273112	TIGR00512, methylthioribose-1-phosphate_isomerase_predicted, S-methyl-5-thioribose-1-phosphate isomerase. The delineation of this family was based in part on a discussion and neighbor-joining phylogenetic study, by Kyrpides and Woese, of archaeal and other proteins homologous to the alpha, beta, and delta subunits of eukaryotic initiation factor 2B (eIF-2B), a five-subunit molecule that catalyzes GTP recycling for eIF-2. This clade is now recognized to include the methionine salvage pathway enzyme MtnA. [Amino acid biosynthesis, Aspartate family].	1.41633e-120
NZ_CP023992.1\|WP_099013972.1\|4034519_4035998_+\|ATP-binding-protein	gnl\|CDD\|226967	COG4608, AppF, ABC-type oligopeptide transport system, ATPase component [Amino acid transport and metabolism].	0.00556041
NZ_CP023992.1\|WP_099013980.1\|4049473_4051753_+\|PTS-transporter-subunit-EIIA	gnl\|CDD\|224218	COG1299, FruA, Phosphotransferase system, fructose-specific IIC component [Carbohydrate transport and metabolism].	2.39599e-111
NZ_CP023992.1\|WP_099013984.1\|4056735_4058094_-\|phosphomannomutase/phosphoglucomutase	gnl\|CDD\|236557	PRK09542, manB, phosphomannomutase/phosphoglucomutase; Reviewed.	0

>NZ_CP023992.1|WP_099013980.1|4049473_4051753_+|PTS-transporter-subunit-EIIA
MTSPADPPNGAGASGPGLKLLAVTACPTGIAHTYMAAEKLAQAAESLGHSMKVETQGSIGAENVLSDNDVSDADGIIIAADKDVDRGRFVGKRVLVVGVADGIHRPERLIEQVLDAPVYEGDGQDAGRGAASAGRGSGGGGGRAGGGGSGGSGKGRSITYKALMNGVSYMIPFVVVGGLLIAVSLALGGDTTSKGIVIPDDSFWKTVNDIGSIGFELMIPALSGYIAYAIADRPALVPGMVGGWIAAHGDLYDSEAGAGFIGAIVTGFLAGYLVLWIKRIRVPKFVQPIMPIIVIPIVATSALGLFFIYVLGEPISWVFENLTDWLGGLTGTSAALLGIILGLMIAFDMGGPVNKTAFLFGAGLVSKNPEVMGACAAAIPVPPLGQGLATLLRRRMFDDQERETGLAALFMGFFGITEGAIPFAAARPARVIPANMLGGAVAGAIAGVASVEDNVPHGGPIVAVLGAIGGVPMFFVAVVGGTAVTALVTIALMSVGEGRGGAADADADAAGAVGAADADAAGAASVGLSAAGEPVLAGVGGGGAGGGGAGGGGAPGASGVGVASVEASGAGASGAGAVRKAVGSEAGSVRGGEGAAAFEDAADAGSARQVLSGYLTERTVKERLAADGKDAAIREMAELLAATGKVVDTAELVRAAFAREDQGTTGLGEEIAIPHAKTDAVTAPVVGFARSPEGIEWGAPDGTKARLVFMIAVPEAAAGDEHLRILALLSRKLMGAEFRERLLGAGDVGAILGVLGEIE
>NZ_CP023992.1|WP_069871094.1|4047606_4049064_-|adenosylhomocysteinase
MTKAVSGQDFKVADLSLAAFGRKEITLAEHEMPGLMSIRKEYAEQQPLAGARITGSLHMTVQTAVLIETLVALGAQVRWASCNIFSTQDHAAAAIAVGPEGTAENPQGIPVFAWKGETLEEYWWCTEQALTWPGTPTGGPNMILDDGGDATLLVHKGVEYEKAGAAPDVATAENDEHRVILELLNRTIAENPRKWTQLASEIRGVTEETTTGVHRLYEMQRDGSLLFPAINVNDAVTKSKFDNKYGCRHSLVDGINRATDVLIGGKVAVVCGYGDVGKGCAESLRGQGARVIITEIDPICALQAAMDGYQVATLADVVETADIFITTTGNKDIILAADMAKMKHQAIVGNIGHFDNEIDMAGLAAVPGIVKDEVKPQVHTWTFADGKKIIVLSEGRLLNLGNATGHPSFVMSNSFANQTIAQIELFTKPESYPTDVYVLPKHLDEKVARLHLDALGVKLTTLRPEQASYIGVPVEGPYKPDHYRY
>NZ_CP023992.1|WP_099013979.1|4046855_4047473_-|hypothetical-protein
MPRGRYSLHDPHDHTPLGEEHFQCAPGPSGWRYVAQRTAPSGDHSGSVDLTLDELGRPLRVELHSASWQVRGAALDGVTWVRTDPTGAHATEGNVRAHSFTGASPAFLIAVSRLLRLEPGAGAVRVRLVAFTDPVLAPITLDQSWALLDRTGHATDTGPLVVDEYQVIEVDTGEVRTVHIAGDVVLAAPGIELEELESPPSSFAA
>NZ_CP023992.1|WP_099013977.1|4039531_4040797_+|hypothetical-protein
MNDSPGWAPPGSSPSDEPDHDAQEQGKPADQPAPEQPVWGAQWARRQPPPGSWAASGGRPTPPPGPHAPPPGGWGTGRRQSAAPRPGVIPLRPLSIGEILDGAVAIMRAHWRTVLGISLIVSIVTQGLITAATGLWFNDARGNESDVLNDPDATIGQAMRAVGDSLGDSGVTLLLGVLGTIVTTALLTVVAAQAVLGRSVSTKEAWAGARPRLLQLCGLLLLVPTIAVAIIGAGMTPGLLLAAAGVPSEGAALASLGGLAGAGVAAWLWVRFSLAAPALMLEKQGIVKALRRSFKLVRGAWGRVFGIQLLAVVLVFIVGAIIEIPTSLVAMMIGGDNAMDWLSGESVSVGWTFLIVVGVGGVISSTITFPISAGVTALLYMDQRIRREALDLELARAAGMPEGSAGANGEGQPTVGSTSGN
>NZ_CP023992.1|WP_099013976.1|4038224_4039382_-|S-methyl-5-thioribose-1-phosphate-isomerase
MADQYPVSPEGSIPPTALALRWEEPPEGPVLVLLDQTRLPAEEVDLVCTDVPALVEAIRSLAVRGAPLLGLAGAYGIALAAARGFDVDEAAESLAHARPTAVNLAYGVRRAAAAYHAAIRDDADEARAAAAALAEARALHREDAEASDRMAAHGRALLDELLPAGGHRILTHCNTGALVSGGEGTALAVVKAVHRAGQLRRLWVDETRPLLQGARLTAYEAARAGMAYTLLADNAAGSLFAAGEVDAVLIGADRIAADGSVANKVGSYPLAVLARYHHVPFVVVAPTTTVDPATADGAGIEVEQRPGYEVTDITIPYAPIAGHEAGTGVPVAPLGTQAHNPAFDVTPPELVTAIVTEHGVLSPVTADGVAELCARSRSGNGMMSA
>NZ_CP023992.1|WP_099013975.1|4036950_4038156_+|tyrosine-type-recombinase/integrase
MARRRPNGAGTVTKRSDGRYQAAVYVPQPDGTTKRKFAYGNDYDECDAKRRKLIERVQNGVPTPTRDMTMGDWFDYWLTSIVKPSLSDGSHRTYESAIRLHLRPRLGRKVMLKLGVKELRAVMTKLAEDKGAKTARHAHRVLKASLTAAMVEDIGLTRNVAKLVHVRASTDSGKSWDAVKVLRFLAEARRRTVYYPALLLIPLLGLRRAEICGLRWENIDLEKRVLWVEQQRQRTSAGTIDVETKTETSRAPLPLPAQCIAPLRWQRMRTAWLRERALASGRPWTDDPDGHVFVTRTGQPLQADCLYQTVQRVTGTAGLGKMNPKGLRKSCGTLLVHLRVHPRIVKAVLRHSRISTTLDIYAEALDPDVIEAIGQLDLLLRQPDRLDRLQTVTSEDDEQPD
>NZ_CP023992.1|WP_099013974.1|4036621_4036951_+|helix-turn-helix-domain-containing-protein
MTQKSEPRTDANSRGRPPPRKVRIGPLDAWTHFPQGDTALSAVITPAPFDESTEALTPREAMTALRIGRDTLYNLIRSGELRSFTIGRARRIPAAEIPAFIRRRMEENH
>NZ_CP023992.1|WP_099013973.1|4036020_4036233_+|hypothetical-protein
MAFRFTINSPNGAVSLTAEAVTLRHASDHPEPAVAIRITRGHMLYVPLDRIEELVTGIRDTGRQAADPSR
>NZ_CP023992.1|WP_099013972.1|4034519_4035998_+|ATP-binding-protein
MSDDEKNPARDVITDYAQAHFRYFRTADGTVYAQKNGHPVARPIRSQGTTGSHRQELMVGLYRDGRGVFNGTALKEALDLIEALALSEDVQPVHIRVAPGFDGATWLDLGRNDGQSVRIHPTGWDIVVPDPREVCWRRTQLTGELPLPAKDTEGKGIDLLLRLCNFANAETECLAIAWLIGCLGPSVPVPAPFLTGPQGAGKSTGGRMLVRIIEGMSGDLRRAPKDEENLIAAVAAGWVTALDNLSHMTPDLSDAMCRIVTGAEDVKRALFTDGDVFRARYRRPLLLTGIDVGVIRPDLAERLLPLRLERPRVRRTEDELWTEYEKVLPVVLGSLLDLTVKVRAVEAETPTDLRMADFAHLCAQLDAATGLGALNAYRASLDDLNDDVIEGDLLAQTVLRHADSIEPGAAQRMTSTEWLHCLSRLYSGDELRPLPRGWPTTGKVLSDRLKRLQPTLAARRVLIDWGRTSEGRYLEMTRQPAPPAPYQQEQMH
>NZ_CP023992.1|WP_099013971.1|4033677_4034517_+|bifunctional-DNA-primase/polymerase
MNKHLHTALSLAADGLPVLPLRKGKVPFGNCPACAQNACGGRPNMKTPGPCTCPAPCHGWAAAATDPHTINAQTWATAWREAAAVAYHPGGAGLTVVDLDNAAAVAWARETLPATRTVATTRGEHWIYQGAMRSVNAVRDGVDIKSTMAYARWLGPGAGTMTALPAVVHALAVKELSTVRPAPQAIAVPTRTGEGPCRHRTPAYLERGIAMAEQRITEARSAVHATVYRTFLAVLSTHGRCGCLTEAHIARLFTAAQAKGESPRHCTDAWTNARTTLGL
>NZ_CP023992.1|WP_099013981.1|4052532_4053468_-|cation-diffusion-facilitator-family-transporter
MSASGGTKAIGAALGANLAIAVAKFVAFAFSGSSSMLAEGVHSIADSGNQGLLLLGGKKAKREATPEHPFGYGRERYIYGFLVSIVLFTIGGVFALYEGYEKIQHPHELEHWYWPVGVLLFAIIAEGFSFRTAIKESNEIRGRLSWPEFVRRAKAPELPVVLLEDFGALVGLVLALGGVGLSLLTGDGVWDGIGTLCIGTLLVLIALVLAAETKSLLLGEAADATQVGKIREAVVDGDTVTAVIHMRTLHLGPEELLVAAKIAVQHDDTAAEVAHAIDAAEARIREAVPIARVIYLEPDILRTSTSTTTPA
>NZ_CP023992.1|WP_099013982.1|4053573_4054770_-|mannose-6-phosphate-isomerase,-class-I
MDRLANTVRPYAWGSTTAIPELLGVQPTGEPQAELWMGAHPGAPSRVDRGAGSVALSEVIAADPEGELGADAVRLFGPRLPFLLKVLAAGSPLSLQVHPDLAQAKEGFADEEERGVPIDAAHRNYKDANHKPELICALTPFNGLCGFRDPNEAAELLAALEVDSLKPYVDILHAHPESHALREVLTAVLTADPEAMAETVRQASVAAERLGALDGPYAPAYAAYASIARHYPGDPGVIAAMLLNFVTLQPGEALYLGAGVPHAYLDGLGIEIMANSDNVLRCGLTPKHVDVPELLRIVRFESAAPAVLRPEADPSGEELYTTPIDEFRLSRHVLADGADPRPLPTTGPQILLCASGEVSLRGADGELPLTRGQSAFVPAGERASLSGDGTVFRATVTA
>NZ_CP023992.1|WP_099013983.1|4054905_4056210_-|mannose-6-phosphate-isomerase
MLDESLLDAPEALARADTRGLLRGAAESGARVRTAARHAAEAGIGDLKPDGRPRAVMVAGPGAAGSCTADLLGALSGGNCPVSLIVPTGVAPAPGALRWALPGWAGPLDLLVLATPDGTEPGLPRLVEQAYRRGCAIVAVAPDRSPLADAVAQARGLMVPLATASDNSAPYATGGYGTDPYRRDPLAPGAAEEDTALAEGALGDAPAPYGTPSVPQPVEPPGTAPDEMTGPALPGTLWALLTPLLLLVDRIGLVSAPPTALQQVADRLDQVAERCGPAIATYTNPAKTLAAELAGALPLLWTEGPVAAATGRRFSELLAALAGRPALVAELPGALAAHGALLTGAFAGGADPDDFFRDRVDEPEALRARIVLLHDEPVGPVSAVPTARELALAHETAFSELEPAEGTLLESAAELLAITDFAAVYLALASADRT
>NZ_CP023992.1|WP_059149235.1|4056289_4056472_-|Trm112-family-protein
MPLEAGLLEILACPACHAPLREEQSPETPELVCTGEGCGLAYPVRDGIPVLLVDEARRPA
>NZ_CP023992.1|WP_099013984.1|4056735_4058094_-|phosphomannomutase/phosphoglucomutase
MPDLSQIVKAYDVRGVVPDQWDESLSELFGAAFARVTGADAIVVGHDMRPSSPGLARAFARGAASLGVDVTEIGLCSTDQLYFASGYLGLPGAMFTASHNPARYNGIKMCRAGAAPIGQDTGLADIRALVEEWAGTGAPEPAAESGTITQRDVLADYAAHLRTLVDLTAIRPLKVVVDAGNGMGGHTVPTVFEGLPLELDALYFELDGTFPNHEANPLDPKNIVDLQARVRETGADIGLAFDGDADRCFVVDERGEPVSPSAVTALVAARELAKHPGGTVIHNCITSWSVPEVVKENGGSPVRTRVGHSFIKAEMARTGAIFGGEHSAHYYFRDFWNADTGMLAALHVLAALGGQKGPLSDLVGQYDRYAASGEINSTVDDQTGRMEAVKAAYEGREGAELDELDGLTVTTADWWFNLRPSNTEPLLRLNVEARDTETAAGVRDEVLSIVRA
>NZ_CP023992.1|WP_069871081.1|4058250_4059867_-|L-lactate-permease
MFVQQLDPVADSLSLSALVAALPLFTVLALLGGVRMRAHYAGPIGLVVAALVAWLPYGMPVGQTLSSAAQGVLFGLFPIMWIVVNALWVYRMTVRTDHFDVLRRSFGGLSDDPRVQALVIAFCFGALLEALAGFGAPVAICSVMLVALGFDPVRAAVVALVANTAPVAFGAMATPVVTLAQVTGLPLDSVASVVGRQTPLLALVVPLLLVVIVDGRRGLRETWVPALACGVAFAIAQFTVSNYLSVQLADIAAALVGAAVLMAVPAARRPAEEPVRAAVLTGVRSDDLDHEDPRPEVLRAYAPYALIVAIFSIAQIGPVKDLFAKATRTFDWPFLDVAAPDGKPVGANVFSMPLIATGGTLVLVAGVATAAVLRVNAGDALREWGATVRELRHAILTVVSVLALAYVMNLSGQAATIGHFVAAAGAGLAFLSPVLGWFGVAVSGSDTSANALFGSLQVTAARESGLSADLLAAANSSGGVLGKMISPQNLAIACAAVGLKGREGDLLRKVLPWSVALLLVMCLIVVAQSSFLLGWMLP
>NZ_CP023992.1|WP_069871078.1|4060082_4060532_-|DUF3499-domain-containing-protein
MESRRGPLKSAVPSNVVSPVRRCSRTACGRPAVATLTYVYADSTAVLGPLATYAEPHCYDLCSEHSERLTAPRGWEVVRLAVDTGPPRPSGDDLEALANAVREAARPQERAAGAAAGSGGPGAGHGGREGDPREVPRRGHLRVLRSPES
>NZ_CP023992.1|WP_069871076.1|4060873_4061293_+|metallopeptidase-family-protein
MRGPIAPPQVPLSISRAESFVDLVQDSAERLERRWPQLSGVDFTVLEVPTSGLGGPGSGGGPDGHGGADGWDGESVPLGRFIAARGDTPDRIVIYRRPVEIRAKNRDERALLVHEVVVEQVAELLGLAPESVDPRYGQE
>NZ_CP023992.1|WP_099013985.1|4061422_4062985_-|hypothetical-protein
MNRTTLSLIGAATALAAISGVAALTGGSSEDAGSAGKAATRLPVQRSTLLCPTPSTSDVSSTTYTAYTPKRDGVDAKDGTAELLPAQNAADDVTDPGGDGKGDKNDKNDKSGKDGGKGGDKPVLPLKEPGKPVTTDVSSADAPALIGTADGRFAPGWTVQQTTTIDAGSGRGILGTACTAPDTDFWFPGVSTDRGRQDFVHLTNPDDAAAEVDLKLYGPSGRLKSATDESITVPPRSTLPVLLSTLTDQRAESASLRVTARSGRIGAEVQAVDQKAGSDWLPPSAVPSSSVAIPGIPKDATSARLVVFAPGSDDADLKVRLAGPNNSITPAGHESLHVKSGMTAAIDLGDVTKGEPGSLLLTPEGGEGPATPVVAALQVTRGKGGDQETAFIPATAAIERSATAADNRTKGSTLSLVAPRAAAKVRITASAGAGGGSPVSKTYEVKGGTTKALEPPRPASGKGPYAVTVERLSGGPVHASRMLELTQDGVPMFTIQSLPDDRGTVVVPEAGQNMSLLNDD
>NZ_CP023992.1|WP_099013986.1|4062981_4067046_-|glycosyltransferase
MSVHSHSAAQYPAATAAFAPAQEQAQTPAYPRHVVTAVLVAHDGARWLPDALSGLLGQERPVQSVVAADTGSADDSARLLTETLGEDRVLHMARRSGFGTAVAEAVRTAPVLGPEELAYLKRPSGWDPVNRTWRDDAYDMPELPHGEPIQWLWLLHDDCAPEPDALAELLRVVDAEFTANREPAIVGPKLRGWYDRRQLLEVGVSIARSGRRWTGLERREQDQGQHDQVRPVLSVSSAGMLVRRDVWEQLGGFDSRLPLMRDDVDLCWRAQAAGHQVLIAPDAVLRHAEASARERRPIDCVGRSAHPSPDHHPPRRRFASRSSSPHRVDKAGAVYTLLVNTRGALLPYVMLRLLLGTLLRTLAYLVGKVPGQALDEVAGLFGVLLRPGRILAARKRRGRPATEPSELRPLFPPPGATVRATVEQVASNIGGRSEPELSSGGRHGAVESGPGDDDADFLEVEQFARLKRVARKPGPMLFLVLLVVSLVACRDLLGAGALAGGALLPAPAHVSDLWSSYVDGWHPVGTGGTQSAPPYLAALAALATVFLGSTGFTLTLLLVCSVPLAGFIAYFASRPLVESRLLRAWGSVAYAFLPAATGALAGGRLGTAVLAVLLPLMARAAAAATGFTSNGSKLPSWRATWAYALLLTFTMAFTPVVWPMALLLGVGVLALRQRQSGTEQLMGYGLRFLSVIVTPLVVLAPWSLDLLTDPARFLEEAGLDRGASSASALQLLALSPGGPKGGGTLLLLGFVLAALAALMRGERQTVVRTAWVVALTGFLFAALTGGSGWAGPATLVYGLALLIAGVVGAEGARERVAAQSFGWRQPVALLIAVATVAAPLYAAVSWMASGADGPVGRRDPSQVPAFVAAESATEDQARTLVLGGGSSAARADYALVRGSGARLGDGELAAKGYSDSGLDGVVANLIAGSGADQTRQLGGYAVRYVYVQKGAPPEMERVLNATPGLTQLSREHGGVLWRVDQRVSRVSIVPAESSGRPAGGAAAKPVHVASGPVEAHTTVPDGAAGRVLRIADRSAPDWQATLDGEPLKPTTVDGWAQGFELPANGGRLDLTYDAPLTHTAWVWAQGLLAVVLLVLALPGRRRNVDDDLPDAESAAAVITAEDLAGDGRRARRLRAAAEAQAAQTGQADAAKGRPEADPAAADALPPQPDALPSQPGGIPPQPGEPPLAPPVEPPAMGDPYGDQAAAHDPYGDQAAAGDPYAAVPHQQEYGQEYGQEYERQWDAQTYAEAGYGQYPAGQYQGEQYRGEGYADQYQAGDYQGGYQDTGYPAGYQDGQYPAQEGQYPADPYAGGQYADPYGYDQQQPYTDGGYPAQGDTTYGGADPEDRRDGSEQQR

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Crispr_ID: NZ_CP023992_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_8

4207756-4207866

Orphan

Consensus_repeat	Method
CGTCTCGCGCCTTCGGCGCACTTGAGCAGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_8

>merge|NZ_CP023992|8|4207756-4207866|CRISPRCasFinder
CGTCTCGCGCCTTCGGCGCACTTGAGCAGCAGGGCGGGGGTGGGGCGCGGCGGGGGCCGTGTTCGTCGTCGGGTGCGGCGCCGTCTCGCGCCTTCGGCGCATTTGAGCAGC

>NZ_CP023992|8|8|4207756-4207866|CRISPRCasFinder
CGTCTCGCGCCTTCGGCGCACTTGAGCAGC	AGGGCGGGGGTGGGGCGCGGCGGGGGCCGTGTTCGTCGTCGGGTGCGGCGC
CGTCTCGCGCCTTCGGCGCATTTGAGCAGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069870321.1\|4218446_4219667_-\|amidohydrolase	unknown	unknown	gnl\|CDD\|349936
NZ_CP023992.1\|WP_079257947.1\|4212848_4214144_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224005
NZ_CP023992.1\|WP_099014029.1\|4204288_4204864_+\|VanZ-family-protein	unknown	unknown	gnl\|CDD\|377417
NZ_CP023992.1\|WP_079257948.1\|4215264_4216989_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226364
NZ_CP023992.1\|WP_099016960.1\|4201989_4203564_+\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP023992.1\|WP_099014027.1\|4199433_4200075_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|223645
NZ_CP023992.1\|WP_069870292.1\|4201193_4201880_+\|two-component-system-response-regulator-AfsQ1	unknown	unknown	gnl\|CDD\|223816
NZ_CP023992.1\|WP_099016961.1\|4208630_4209947_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340882
NZ_CP023992.1\|WP_079257942.1\|4200219_4201002_-\|SigE-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|132028
NZ_CP023992.1\|WP_069870319.1\|4217038_4218073_-\|BMP-family-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|380577
NZ_CP023992.1\|WP_099014030.1\|4211117_4212395_-\|thymidine-phosphorylase	unknown	unknown	gnl\|CDD\|180276
NZ_CP023992.1\|WP_069870302.1\|4205254_4205485_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235082
NZ_CP023992.1\|WP_099014031.1\|4219877_4221062_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014028.1\|4203560_4204175_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_079257943.1\|4205609_4206776_-\|adenosine-deaminase	unknown	unknown	gnl\|CDD\|236480
NZ_CP023992.1\|WP_069870300.1\|4204924_4205128_+\|PspC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377200
NZ_CP023992.1\|WP_079257946.1\|4212429_4212852_-\|cytidine-deaminase	unknown	unknown	gnl\|CDD\|180142
NZ_CP023992.1\|WP_069870675.1\|4210165_4211053_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176125
NZ_CP023992.1\|WP_069870317.1\|4214140_4215268_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226962
NZ_CP023992.1\|WP_079153557.1\|4206879_4207644_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|224423

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069870321.1\|4218446_4219667_-\|amidohydrolase	gnl\|CDD\|349936	cd08014, M20_Acy1-like, M20 Peptidase aminoacylase 1 subfamily. Peptidase M20 family, uncharacterized subfamily of uncharacterized bacterial proteins predicted as putative amidohydrolases. These are a class of zinc binding homodimeric enzymes involved in hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. Aminoacylase 1 (ACY1) breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine).	3.83346e-176
NZ_CP023992.1\|WP_079257947.1\|4212848_4214144_-\|ABC-transporter-permease	gnl\|CDD\|224005	COG1079, COG1079, Uncharacterized ABC-type transport system, permease component [General function prediction only].	1.28689e-78
NZ_CP023992.1\|WP_099014029.1\|4204288_4204864_+\|VanZ-family-protein	gnl\|CDD\|377417	pfam04892, VanZ, VanZ like family. This family contains several examples of the VanZ protein, but also contains examples of phosphotransbutyrylases.	3.38445e-13
NZ_CP023992.1\|WP_079257948.1\|4215264_4216989_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|226364	COG3845, COG3845, ABC-type uncharacterized transport systems, ATPase components [General function prediction only].	0
NZ_CP023992.1\|WP_099016960.1\|4201989_4203564_+\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.00014e-54
NZ_CP023992.1\|WP_099014027.1\|4199433_4200075_+\|ATP-binding-protein	gnl\|CDD\|223645	COG0572, Udk, Uridine kinase [Nucleotide transport and metabolism].	1.0771e-21
NZ_CP023992.1\|WP_069870292.1\|4201193_4201880_+\|two-component-system-response-regulator-AfsQ1	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	4.21055e-81
NZ_CP023992.1\|WP_099016961.1\|4208630_4209947_-\|MFS-transporter	gnl\|CDD\|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.2627e-71
NZ_CP023992.1\|WP_079257942.1\|4200219_4201002_-\|SigE-family-RNA-polymerase-sigma-factor	gnl\|CDD\|132028	TIGR02983, putative_RNA_polymerase_ECF-subfamily_sigma_factor, RNA polymerase sigma-70 factor, sigma-E family. This group of similar sigma-70 factors includes the sigE factor from Streptomyces coelicolor. The family appears to include a paralagous expansion in the Streptomycetes lineage, while related Actinomycetales have at most two representatives.	2.63234e-65
NZ_CP023992.1\|WP_069870319.1\|4217038_4218073_-\|BMP-family-ABC-transporter-substrate-binding-protein	gnl\|CDD\|380577	cd06354, PBP1_PrnA-like, periplasmic binding domain of basic membrane lipoprotein, PnrA, in Treponema pallidum and its homologs from other bacteria and Archaea. Periplasmic binding domain of basic membrane lipoprotein, PnrA, in Treponema pallidum and its homologs from other bacteria and Archaea. The PnrA lipoprotein, also known as Tp0319 or TmpC, represents a novel family of bacterial purine nucleoside receptor encoded within an ATP-binding cassette (ABC) transport system (pnrABCDE). It shows a striking structural similarity to another basic membrane lipoprotein Med which regulates the competence transcription factor gene, comK, in Bacillus subtilis. The members of PnrA-like subgroup are likely to have similar nucleoside-binding functions and a similar type 1 periplasmic sugar-binding protein-like fold.	2.27805e-85
NZ_CP023992.1\|WP_099014030.1\|4211117_4212395_-\|thymidine-phosphorylase	gnl\|CDD\|180276	PRK05820, deoA, thymidine phosphorylase; Reviewed.	0
NZ_CP023992.1\|WP_069870302.1\|4205254_4205485_-\|hypothetical-protein	gnl\|CDD\|235082	PRK02888, PRK02888, nitrous-oxide reductase; Validated.	4.71127e-05
NZ_CP023992.1\|WP_069870317.1\|4214140_4215268_-\|ABC-transporter-permease	gnl\|CDD\|226962	COG4603, COG4603, ABC-type uncharacterized transport system, permease component [General function prediction only].	1.44305e-79
NZ_CP023992.1\|WP_079257943.1\|4205609_4206776_-\|adenosine-deaminase	gnl\|CDD\|236480	PRK09358, PRK09358, adenosine deaminase; Provisional.	1.05246e-154
NZ_CP023992.1\|WP_069870300.1\|4204924_4205128_+\|PspC-domain-containing-protein	gnl\|CDD\|377200	pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.	6.22859e-22
NZ_CP023992.1\|WP_079257946.1\|4212429_4212852_-\|cytidine-deaminase	gnl\|CDD\|180142	PRK05578, PRK05578, cytidine deaminase; Validated.	3.02494e-68
NZ_CP023992.1\|WP_069870675.1\|4210165_4211053_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|176125	cd08434, PBP2_GltC_like, The substrate binding domain of LysR-type transcriptional regulator GltC, which activates gltA expression of glutamate synthase operon, contains type 2 periplasmic binding fold. GltC, a member of the LysR family of bacterial transcriptional factors, activates the expression of gltA gene of glutamate synthase operon and is essential for cell growth in the absence of glutamate. Glutamate synthase is a heterodimeric protein that encoded by gltA and gltB, whose expression is subject to nutritional regulation. GltC also negatively auto-regulates its own expression. This substrate-binding domain has strong homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.14072e-86
NZ_CP023992.1\|WP_079153557.1\|4206879_4207644_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	5.34631e-06

>NZ_CP023992.1|WP_079153557.1|4206879_4207644_+|alpha/beta-fold-hydrolase
MAQQALPERGARLGRPMGAAAARRTVHGVVLLLPEGEPNGTRRPSRLSVAATLPLARRLVRAGREEGLAAHVVHYRRRGWNGVAADAASDAAWAVEEVVRRYGDVPICLIGHGMGGRAALRAAGHAAVTSVVALAPWLPAPDELLEPEPVKQLVGRQVLIAHGTNDERTDPELSYRLAERAKKANRDVCRFEVHTDGHGLHQHRSEVQALAVDFLLGTLFHSGFSRPVADALAAPPPLGLRMPLASGFGANLGH
>NZ_CP023992.1|WP_079257943.1|4205609_4206776_-|adenosine-deaminase
MTSEHSHEPTPEQIRRAPKVLLHDHLDGGLRPGTIVDLARETGYDALPETEPDKLGVWFREAADSGSLERYLETFSHTVGVMQTRDALVRVAAECAEDLAEDGVVYAEIRYAPEQHLEGGLTLEQVVEAVNEGFREGERRAFENGHRIRVGALLTAMRHAARALEIAELANRYRDLGVVGFDIAGAEAGFPPTRHLDAFEYLKRENNHFTIHAGEAFGLPSIWQALQWCGADRLGHGVRIIDDIEVADDGSLNLGRLASYVRDKRIPLELCPTSNLQTGAASSYAEHPIGLLRRLHFRATVNTDNRLMSGTSMSGEFQHLVSTFHYTLDDMQWFTVNAMKSAFIPFDERLAMINDVIKPGYAELKSEWLFRDVASASAVTRGSAAAGD
>NZ_CP023992.1|WP_069870302.1|4205254_4205485_-|hypothetical-protein
MKQGTLKTLGAIALGAAAVVAAGGAASAAPAPGAGSVGAPGQSAAKPAVPQAKPGQGMLGQLPLSGLPTGNLIKLG
>NZ_CP023992.1|WP_069870300.1|4204924_4205128_+|PspC-domain-containing-protein
MSAPLVRPRHDKKIAGVCAGLARRFGTTPTTMRVLFVVSCLLPGPQFLLYLALWFLLPAEDSYREAW
>NZ_CP023992.1|WP_099014029.1|4204288_4204864_+|VanZ-family-protein
MQGPFGRRAAFRYRAAGFLLLVAHLSFVCWLTLRPVNVPWVSPATLEPLATIRADLALSPWSAARSIGGGLLLLAPLGVLLPLAAGRVEVYPLASLVRTAFTGAMVALGVALLRSEVTGQIMNMDSVLLNTAGVVLAHLLVVPAVRACLRRRAYRRRTAPLPRDDGTQAPTPTIPRVGIAPWSDVSSGTRT
>NZ_CP023992.1|WP_099014028.1|4203560_4204175_+|hypothetical-protein
MSARWKRSAALLLTGAVALLAAGCGIRGTSVPVDAGAAPSRASCRAPASEQTAEGIGRTSVRIYLLCSSRILSVSRAARLGDEKTAPEPVRVAQALLEQLRLPPTAAEAAAGFSTAVEDWVEITGPAKDDPDNALRLNRPPEEIQSLALAQIICTFADTAVAGDDGKVVLGGPDSQRDPLKAYQCTEEMRRNPVIAVNSGVLVS
>NZ_CP023992.1|WP_099016960.1|4201989_4203564_+|HAMP-domain-containing-histidine-kinase
MRWFSLRLRLMLVFGLVALTAAVSASAIAYWLNRDAVLTRTQDAALDEFRKSLKDDTDPLPSLPTCSELRDVAVRMADNTQKYEVLLITRTRDGESCPAASDKKLFTLDAVPAALRRAVDQKRPVSKGNSAPYHLYWQRITLHGTPYLVGGAKVNGGGPTGYMLKSLDTERQDLNSLAWSLGIATGLALIGAALLAQAAAATVLRPVQRLGEAAHRLGEGHLDTRLQVSGSDELANLSHTFNRAAERLQKRVAELSAREASSRRFVADMSHELRTPLTAITAVTEVLEEEADSLDPMIAPAVQLVVSETRRLNDLVENLMEVTRFDAGTARLVLDDVDVADQVTACIDARAWLDAVELDAARSIVARLDPRRLDVILANLIGNALKHGGSPVRVSARTEGDELLIRVRDHGPGIPEDVLPHVFDRFYKASASRPRSEGSGLGLSIAMENAHIHGGDIGAANSPEGGAVFTLRLPMDASRIASDEAADDPDRDRDGAFAGDGDDDGGGGDNGPAKGPGRNEGGRP
>NZ_CP023992.1|WP_069870292.1|4201193_4201880_+|two-component-system-response-regulator-AfsQ1
MTNVPFLLLIEDDDAIRTALELSLSRQGHRVATAATGEDGLKLLREQRPDLIVLDVMLPGIDGFEVCRRIRRTDQLPIILLTARSDDIDVVVGLESGADDYVVKPVQGRVLDARIRAVLRRGEREANDSAAFGNLLIDRAAMTVTKNGEDLQLTPTELRLLLELSRRPGQALSRQQLLRLVWEHDYLGDSRLVDACVQRLRAKVEDVPSSPTLIRTVRGVGYRLDAPQ
>NZ_CP023992.1|WP_079257942.1|4200219_4201002_-|SigE-family-RNA-polymerase-sigma-factor
MSTLHFTNTSAVRTRLHDAGRGNEKSGAVSGRGCARGAGRQRPPYMVAIDAITGDKEAGTGLGGDDGGPGGHGGGSYGEAEGERRTTSEAEFTAYVQERRASLYATAYHLTGDRFEAEDLLQSALFSTYRAWDRISDKAAVGGYLRRTMTNLHISAWRRRKLNEYPTEELPETVGDHDAMRGTELRAVLWQALARLPELQRTMLVLRYYEGRTDPEIADILNISVGTVKSSIWRSLRRLREDEILSFGRDEEESFGELVA
>NZ_CP023992.1|WP_099014027.1|4199433_4200075_+|ATP-binding-protein
MTSQPPSARVVLLSGPSGSGKSSLAARAGLPVLNLDDFYKGGGDPTLPQLADGGGADWDSPLSWDADAAVAAVEALCRTSRTTVPLYDIATSARVGEEALDIGPAPLFIAEGIFAADIIGRCADLGVLADALCLRGRPSTTFRRRLLRDLREGRKPALYLLRRGWRLMRTERGIVARQTALGAYACGKGVALGRIAAAAAGGPVPAPGQKASV
>NZ_CP023992.1|WP_099016961.1|4208630_4209947_-|MFS-transporter
MSTNVMSTNSNPSAPSAPSASDAANAPVPERMRPGRPGYSRMRLALFTAGLATFALLYSTQALLPAISDDLRVQADQASWSVSASTFGLALAVIPLSALSERFGRRAMMTVSLTVAVALALLVPFAPDLGWLIALRAVQGAALAGIPASAMAYLSEEVHPKALVGTIGLFVAGNSVGGMSGRILTGWVADAWGWRVALAAVGVMAVVCAVAFRMLLPRPRHFTPAEVSPRALARTLAGHLSDPLLCRLYAIGALFMTVFGGVYTVIGYRLVAQPFGLSQSLIGSIFLIYLVGTFSSAATGKLVGRLGRRGALYAAVSTTAAGLLLSLLNSIPAVLAGLVLITAGFFAGHAAASSAVSRTAKTGRAQAAALYQASYYIGSSVGGALGALAFHAAGWGGTVAMGLVAVVGAAGITLYATRQARAERRAEVARRELCGVPS
>NZ_CP023992.1|WP_069870675.1|4210165_4211053_+|LysR-family-transcriptional-regulator
MALTPRLAQFAAVARHEHVTRAAQELGVPQSTLSRAMVRLEEDLGVALFARRGRTVALTPAGRTFLRSVERALAEVDRAAESVRADADPAAGRVSFGFLHTLGTETVPGLIRGFRADHPRVRFQLVQNYGEAMIERMRAGGLDLCLTSPVPDAPDLVARRLDEQRLRLVVPDDHRLAGRRRVRLAEAASELFVTLEPGYGLRRITDALCAEAGFTPRIAFEGEEAETLRGLVAAGLGVALLPPPAVPRPGVAELTVTAPRAVREIGVAWLDGHPDTPPVAAFKKFLLSRRGQLLP
>NZ_CP023992.1|WP_099014030.1|4211117_4212395_-|thymidine-phosphorylase
MDAISVIRAKRDGTRLTDAQIDWVIDAYTRGEVADEQMSALAMAIFLNGMDRAEIARWTAAMIASGERMDFSSLPRPTADKHSTGGVGDKITLPLAPLVAACGAAVPQLSGRGLGHTGGTLDKLESIPGWRAQLSGADMLAVLRDVGSVICAAGEGLAPADKKLYALRDVTGTVESIPLIASSIMSKKIAEGTGSLVLDVKVGSGAFMKDIDSARELAATMVGLGNDHGVRTTALLTDMSTPLGLTAGNALEVRESLEVLAGGGPADVVELTLALAREMLDAAGLPDADPAKALADGTAMDHWRRMISAQGGDPDAPLPTAREHHVVTATADGVLTRLDAYAVGLAAWRLGAGRARKEDPVQAGAGVELHAKPGDRVTPGRPLLTLHTDTPSAFAYALEALENAIDYAPENSEFTASPIVLDRIA
>NZ_CP023992.1|WP_079257946.1|4212429_4212852_-|cytidine-deaminase
MTTSAAAAPDWESLRVRARDAMSRAYAPYSGFPVGAAALVDDGRTVSGCNVENAAYGVALCAECGLVSSLVASGGGRLTAFTCCDREGAVLMPCGRCRQLLWEHGGPELQMDTATGIRPLAELLPDAFGPADLRRPAAHG
>NZ_CP023992.1|WP_079257947.1|4212848_4214144_-|ABC-transporter-permease
MSATVTTTKSTSAPGKGNGPASRMSLGKVLLIVAGALIALSVLRTLVDAAQQADFDRVTSAGQIGAALSMAVPIGLAGLGGLWSERAGVVNIGLEGMMILGTFFGAWAGYQTNPWVGVLAGVLGGAVGGLVHAVATVTFGVDHIISGVAMNILALGATTYLAKRWFEPLADIGGSPKNSPQVDPIQTFTVPGLSDWLADLENHHWFLVSDIAGVLGGLVTDISALTIVSVLLVVGSFFALWRTSFGLRLRSCGENPTAAESLGVNVYLYKYAAVVISGALAGLGGVFLALVRSHIYNEGQTGGRGYIGLAAMLFGNWRPGGLAMGAGLFGYSDALQLRNGGATVHALLLLVALGLAALAAWRIVRKSYVAGAVSGAAAVALLLWYALTDTVPNDLVSATPYIVTLLVMGLASQRLRMPKANNRPYRKGQGT
>NZ_CP023992.1|WP_069870317.1|4214140_4215268_-|ABC-transporter-permease
MKKLDKERVLLAVAAPVLALAAAFVLTALVLLATGKEPFNAFGIMFDYGMKADSQVYILNKATTYYLAGLAVAIGFRMNLFNIGVDGQYRLAAFFAAVVGGALGLPGLVQIPLILLVGMLVGAMWASIAGLLKVYRGVSEVISTIMLNSLSGIVISYLLVDGRLADLDKQTNIVATDPLPSSSHFFTIPAGGDLDPIWGFIVVAALAGVGFWFLLGRTRFGFDLRAVGRSESAAQASGVNVKRMVLTSMVLSGAMAGLIGMPTLLNDTHQFTSDFPTGIGFTGIAIALLGRNNPVGIALAAVLWGFLERGANRLEFEGYDKEIVGVMQGVIVLCVVIAYELVRRYGLKRQQQRVGAELAAQARADKGSDKQEVPA
>NZ_CP023992.1|WP_079257948.1|4215264_4216989_-|ABC-transporter-ATP-binding-protein
MAYPGRSGPRPAPPPVAPQECAIKAASPPKGAPAGAVTDVAVELHGITKRFPGVVANHDIDITVRRGTVHALVGENGAGKSTLMKILYGMQRPDEGTIAIDGKTVELHSPADAISRGVGMVHQHFMLADNLTVLENVVLGAEKLHGIGGRARARIKEISDAYGLGVRPDVLVEDLGVADRQRVEILKVLYRGARTLILDEPTAVLVPQEVDALFDNLRELKSEGLTVLFISHKLGEVLSVADDITVIRRGTTVASVVPSETSPRQLAELMVGSELPSPETRESTVTDTDMLVVGALRLTATDVDGVQRAVLDDIDFTIHKGEVLGIAGVEGNGQAELVEAIMGMRDPDAGTITLDGADISHAPTRKRREDGIGYIPEDRHRHGLLLEAPLWENRILGHVTEVPNSKGGLLNPAAARRDTERIVAEYDVRTPGIEVTAASLSGGNQQKLIVGREMSHHPKLLIAAHPTRGVDVGAQAQIWDQIRAARREGLAVLLISADLDELIGLSDTLRVMYRGRLVADADPATITPEQLGSAMTGAASGHLEDSADDGTEAATGTASGTGPAAEAATGGEDR
>NZ_CP023992.1|WP_069870319.1|4217038_4218073_-|BMP-family-ABC-transporter-substrate-binding-protein
MRRVSTIAVAGIATAALALSVTACGSSSEEGSKDAGIGLAYDVGGRGDHSFNDSAAKGYDKALKDFDVKGKELTAKDGDTDADRYDKLASLAEAGYNPVIGVGYAWTPSLTKAAKKYKDTDFAIVDSVVDAKNVASLVSAEHEGSYLAGVAAGLKTKSDKVGFIGGTDSALIKKFAGGFQQGLKETNPKASLDVQWVQVGSPKGFGMPDRGKDIAEGMLSNKVDVIFSAAGGSGAGAIEATAGKKGTWSIGVDGDQYYDKGLAQYKNTILTSMIKTVDGSVYDFIQSVVKDKKPESGVQTYDLKRGGVSLSYSGGFINDIKPKIEAAKKKIIDGQIKVQDTYKD
>NZ_CP023992.1|WP_069870321.1|4218446_4219667_-|amidohydrolase
MSLDATDATPATAPALPGTLPDELRTELIAFRRDLHMHPELGNCEFRTTAAIKARLEQAGLEPRVLPSGTGLICDIGPRDGVAPLLALRADIDGLPIPDTKTVDYRSTVADRAHACGHDVHTTVVLGAGLVLAQLAREGRLARPVRLLFQPAEEVLPGGAADAIEAGVLDGVGRILAVHCDPKVEVGRIGLRIGPITSACDRLEVSLDGPGGHTARPHMTTDLVTAAAKVITEVPALLARRVDARSGLAVTWGRVESGHACNVIPQHAELSATVRCLDLPAWREAPDLVHAAVDEIATLHRAKSEINYIRGVPPVVNEASSAELLRDAMIARRGASAVEDTEQSLGGEDFSWYLERVPGAMARLGVRKVGDTTRRDLHAGDFDVDEGSIAVGVELFTAAVLLDRNA
>NZ_CP023992.1|WP_099014031.1|4219877_4221062_-|hypothetical-protein
MVSAAPLAPQATLAFVESPVQLLNVLEWAYSDVQRARRAGGPAATAPQDLTVVVLSPHDPMTRGQLRRMAELARDEGVIVRWEDARGGAGAPIKTIGGLRGPLRRAARIVIGDPFSRYVQLLLTLTRAKDLVVVDDGTATMEFISQLAKGEPLVRWHRRGSHGPRDLVFAPVSATARRRLTPGDKRRVEVFSSMPVEPPAGVTITANDFAWTRSRFGPPRLTGGTDLVGTSLVETGVVDLERYLEAVGSLTRAHGATRYFAHRRESTEKLSRIAHEVGLEIVRPDLPLELIARRGPIGHTIVSFPSTVVHTLPLALVGTGVEVAVCDVDPAWLTSNASPRAQGFLSGVTGTARDVRRLNSGPTAGSPPPRDAAPPRDPAPPANPGPPAAPVAAS

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Crispr_ID: NZ_CP023992_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_9

4452009-4452377

Orphan

Consensus_repeat	Method
GGGTTCGGCCGCGCCGGGCTCGGG	CRISPRCasFinder

6 spacers

The CRISPR arrays of NZ_CP023992_9

>merge|NZ_CP023992|9|4452009-4452377|CRISPRCasFinder
GGGGTCGGGTGCATGGGGCTTGGGTGCGCGGGGGTCGCGTGCCGGGTTCGGCCGCGCCGGGCTCGGGGCGGGGTTCGGCCTGCGAAGTTCGCGTGCACGGGGTCCGGCCGCGCCGGGCTCGGGTGAATCGGCTCGGATGCTGGACTCGGGCGCGCAGGGGTGAGGGGCAGGGCTCGGCGCGGGGTGCCTGCGCAGGGCTCGGCTGCGCGCTATTCGCGTGGGCGGGGTTGGCTGCGCCGGGCACGGGCGCCGGATTCGCGTGCGCGGGGTTCGGATGCACGGAGTACGGGGTTCAGCCGCGCCGGAATCGGGGGCTGGGCTCGGGCGTGCCGATCCCGATGCACCGGGCTCGGATGCGCGGGACCCGGG

>NZ_CP023992|9|9|4452009-4452377|CRISPRCasFinder
GGGGTCGGGTGCATGGGGCTTGGG	TGCGCGGGGGTCGCGTGCC
GGGTTCGGCCGCGCCGGGCTCGGG	GCGGGGTTCGGCCTGCGAAGTTCGCGTGCACG
GGGTCCGGCCGCGCCGGGCTCGGG	TGAATCGGCTCGGATGCT
GGACTCGGGCGCGCAGGGGTGAGG	GGCAGGGCTCGGCGCGGGGTGCCTGCGCAGGGCTCGGCTGCGCGCTATTCGCGTGGGC
GGGGTTGGCTGCGCCGGGCACGGG	CGCCGGATTCGCGTGCGCG
GGGTTCGGATGCACGGAGTACGGG	GTTCAGCCGCGCCGGAATCGGGGGCTGGGCTCGGGCGTGCCGATCCCGATGCACC
GGGCTCGGATGCGCGGGACCCGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069870626.1\|4459957_4461583_-\|chaperonin-GroEL	unknown	unknown	gnl\|CDD\|234573
NZ_CP023992.1\|WP_099014112.1\|4448604_4448934_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014110.1\|4442408_4444058_+\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223989
NZ_CP023992.1\|WP_009716982.1\|4461922_4462129_-\|cold-shock-protein	unknown	unknown	gnl\|CDD\|224197
NZ_CP023992.1\|WP_099016984.1\|4458894_4459836_+\|N-acetylmuramic-acid-6-phosphate-etherase	unknown	unknown	gnl\|CDD\|235467
NZ_CP023992.1\|WP_079258043.1\|4447078_4447807_-\|copper-homeostasis-protein-CutC	unknown	unknown	gnl\|CDD\|225684
NZ_CP023992.1\|WP_069870749.1\|4444561_4446661_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226482
NZ_CP023992.1\|WP_099014116.1\|4454934_4455882_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP023992.1\|WP_099016983.1\|4441199_4441670_-\|VanZ-family-protein	unknown	unknown	gnl\|CDD\|377417
NZ_CP023992.1\|WP_099014117.1\|4456595_4456883_-\|DUF4031-domain-containing-protein	unknown	unknown	gnl\|CDD\|379076
NZ_CP023992.1\|WP_167459920.1\|4450658_4451933_+\|Cmx/CmrA-family-chloramphenicol-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|225371
NZ_CP023992.1\|WP_099014109.1\|4436192_4437479_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235906
NZ_CP023992.1\|WP_079258050.1\|4455884_4456544_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP023992.1\|WP_087684229.1\|4457529_4458459_+\|MurR/RpiR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224651
NZ_CP023992.1\|WP_069870744.1\|4433774_4434860_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl\|CDD\|376439
NZ_CP023992.1\|WP_099014114.1\|4452512_4453859_-\|cation/H(+)-antiporter	unknown	unknown	gnl\|CDD\|223551
NZ_CP023992.1\|WP_099014111.1\|4447863_4448547_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226789
NZ_CP023992.1\|WP_099016982.1\|4434946_4435720_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224045
NZ_CP023992.1\|WP_093701802.1\|4456882_4457239_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014115.1\|4454235_4454568_-\|DUF3040-domain-containing-protein	unknown	unknown	gnl\|CDD\|378610

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069870626.1\|4459957_4461583_-\|chaperonin-GroEL	gnl\|CDD\|234573	PRK00013, groEL, chaperonin GroEL; Reviewed.	0
NZ_CP023992.1\|WP_099014110.1\|4442408_4444058_+\|DEAD/DEAH-box-helicase	gnl\|CDD\|223989	COG1061, SSL2, DNA or RNA helicases of superfamily II [Transcription / DNA replication, recombination, and repair].	1.85269e-106
NZ_CP023992.1\|WP_099016984.1\|4458894_4459836_+\|N-acetylmuramic-acid-6-phosphate-etherase	gnl\|CDD\|235467	PRK05441, murQ, N-acetylmuramic acid-6-phosphate etherase; Reviewed.	1.2825e-159
NZ_CP023992.1\|WP_079258043.1\|4447078_4447807_-\|copper-homeostasis-protein-CutC	gnl\|CDD\|225684	COG3142, CutC, Uncharacterized protein involved in copper resistance [Inorganic ion transport and metabolism].	7.71157e-26
NZ_CP023992.1\|WP_069870749.1\|4444561_4446661_+\|AAA-family-ATPase	gnl\|CDD\|226482	COG3973, COG3973, Superfamily I DNA and RNA helicases [General function prediction only].	6.08504e-71
NZ_CP023992.1\|WP_099014116.1\|4454934_4455882_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.153e-46
NZ_CP023992.1\|WP_099016983.1\|4441199_4441670_-\|VanZ-family-protein	gnl\|CDD\|377417	pfam04892, VanZ, VanZ like family. This family contains several examples of the VanZ protein, but also contains examples of phosphotransbutyrylases.	9.24631e-26
NZ_CP023992.1\|WP_099014117.1\|4456595_4456883_-\|DUF4031-domain-containing-protein	gnl\|CDD\|379076	pfam13223, DUF4031, Protein of unknown function (DUF4031). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and viruses. Proteins in this family are typically between 91 and 130 amino acids in length. There is a conserved HYD sequence motif.	1.87162e-33
NZ_CP023992.1\|WP_167459920.1\|4450658_4451933_+\|Cmx/CmrA-family-chloramphenicol-efflux-MFS-transporter	gnl\|CDD\|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	1.6973e-83
NZ_CP023992.1\|WP_099014109.1\|4436192_4437479_-\|hypothetical-protein	gnl\|CDD\|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	6.75902e-06
NZ_CP023992.1\|WP_079258050.1\|4455884_4456544_+\|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].	1.49548e-69
NZ_CP023992.1\|WP_087684229.1\|4457529_4458459_+\|MurR/RpiR-family-transcriptional-regulator	gnl\|CDD\|224651	COG1737, RpiR, Transcriptional regulators [Transcription].	6.94659e-71
NZ_CP023992.1\|WP_069870744.1\|4433774_4434860_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	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.	7.39755e-68
NZ_CP023992.1\|WP_099014114.1\|4452512_4453859_-\|cation/H(+)-antiporter	gnl\|CDD\|223551	COG0475, KefB, Kef-type K+ transport systems, membrane components [Inorganic ion transport and metabolism].	5.94973e-46
NZ_CP023992.1\|WP_099014111.1\|4447863_4448547_+\|hypothetical-protein	gnl\|CDD\|226789	COG4339, COG4339, Uncharacterized protein conserved in bacteria [Function unknown].	1.3212e-38
NZ_CP023992.1\|WP_099016982.1\|4434946_4435720_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224045	COG1120, FepC, ABC-type cobalamin/Fe3+-siderophores transport systems, ATPase components [Inorganic ion transport and metabolism / Coenzyme metabolism].	1.13331e-132
NZ_CP023992.1\|WP_009716982.1\|4461922_4462129_-\|cold-shock-protein	gnl\|CDD\|224197	COG1278, CspC, Cold shock proteins [Transcription].	1.52185e-34
NZ_CP023992.1\|WP_099014115.1\|4454235_4454568_-\|DUF3040-domain-containing-protein	gnl\|CDD\|378610	pfam11239, DUF3040, Protein of unknown function (DUF3040). Some members in this family of proteins with unknown function are annotated as membrane proteins however this cannot be confirmed.	1.82964e-07

>NZ_CP023992.1|WP_167459920.1|4450658_4451933_+|Cmx/CmrA-family-chloramphenicol-efflux-MFS-transporter
MPSSRTVSARPRMPLAVYVLGLSVFALGTSEFMLSGLLQPVARDMGVSIPTAGLLISAFAIGMVVGAPVLAAATLRLPRRTTLMALLAVFGLGQVAGAVAPSYGVLFASRVVSALACAGFWAVGAAVAVSLVPVNARAKAMAVMVGGLSIANIAGVPAGAILGQHAGWRAAFWAVAGLSVLGLIGVATLVPRTKVPTGDDQPRLRAELRIYRDRQVWLALAATALSGGAVFCLFSYLGPLLTDVAGLDEGWVPTVLALFGVGALLGTVIGGRIADAHLFGTMFWGIVASTAVLSALALTAHSAVAAVTLALMLGFTAFLTAPALNARMFNLANSAPTLAGATNTSAFNIGNTVGPWLGGLVIDAGWGYPAVAWTGAALAGTGAVTTVAAMRLHHAAGASRVIASSAPAASYAPGSRPSQRSETR
>NZ_CP023992.1|WP_099014112.1|4448604_4448934_+|hypothetical-protein
MDDNAVHLDDQALPFWVEVTEDGDDDSMGILGGGNPELRMVPLGPLRKNLAATVDALQQVFADVAARNGTLPLAEAQLSFQVTASGGVQLIGTGQVQGTRGLTLTFKSP
>NZ_CP023992.1|WP_099014111.1|4447863_4448547_+|hypothetical-protein
MPAPAPARHPAHDALLTRWADLLATAREATAEAKTPSPVPYGEDLLTRWAEPQRRYHTTDHLLAVLDRVDELLPHVQAPDPAAVRLAAWFHDAVYLPDRSTNEERSARLAERALTEAAVPAPRTAETVRLVLLTRDHDPAEGDTNGEVLCDADLAVLAGSPEDYGAYAAAVREEYAFVPDDTFREGRANVLRHLLGLPHLFRTPAAHDRWEAPARHNMTTELELLGA
>NZ_CP023992.1|WP_079258043.1|4447078_4447807_-|copper-homeostasis-protein-CutC
MSRPILEVIALNPADAIAAQAGGADRLELVTDMAADGLTPSRETFAAVRSAVDLPVRVMLRASDGFAAGDTAAFDALCEAAAVLHSEGADEFVLGFLTDDGGVDLAAVTALAEVVGAGGGVDESRWTFHRAIDRAADRDGLRKRLADVPGLDTYLTAGAARGVDDGLPTLVEEAARAGTPGYEPRVMVGGGLRLDHLPALRAARIDAFHIGGAARPSGWSGPVDAAVVGQWRTALDAPVPVG
>NZ_CP023992.1|WP_069870749.1|4444561_4446661_+|AAA-family-ATPase
MTGPLADPLANPLADPLADPLARERAHLTASRAALRAMRADVEALDLRDVSANWVNAEALHHQVSERIKALADLADTPLFFGRLDYLHTPGAESAEGAAGERFYIGRRHVHDGDGDPMVIDWRAPVSQPFYQASKKAPMDIGLRRRFGYTGGELTAYEDERLSDPEEAEQTSKLLQSEIERPRVGPMRDIVATIQPEQDEIVRQGIGGTICVQGAPGTGKTAVGLHRVAYLLYAHRERLARSGTLVIGPNRSFLHYIEQVLPALGELQVAQATVEDLVTRPSLGAESRGTDSADAARIKGDARLAEVLRRALRSHVTAPAEPCVVVRGSRRWRVPAYELEEIVEELLTRDIRYGAAREALPQRIAHAVLIRMEQAGEAPDDRVQDAVARNPAVKAAVKAIWPPVDPAKLVLRLLSDADFLAAHADGILDADEQKTILWAKPGRGVKSAKWSPADLVLIDEAADLIERTPSLGHVVLDEAQDLSPMQYRAVGRRCSTGSATVLGDIAQGTTPWATASWEEALTHLGKDGAAVEELTQGFRVPREVIAYASRLLPAIAPGLSEATSIREAAGDFSVRAVDPDELDAAVLAACREALGHEGSIGLIAADARVPALAEALDAAGLTHLSPGEETSAEARLTLVPATLAKGLEYDYVVLDEPAAVVDGEPDERTGLRRLYVALTRAVSGLTVIHGAPLPERLAA
>NZ_CP023992.1|WP_099014110.1|4442408_4444058_+|DEAD/DEAH-box-helicase
MNGPLIVQSDKTLLLEVDHEQADACRRAIAPFAELERAPEHIHTYRVTPLGLWNARAAGHDAEQVVDALVAYSRYPVPHALLVDVAETMARYGRLRLLKHPTHGLVLETSDRPVLEEILRSKKVQPLVGARIDPETVVVHPSERGQIKQTLLKLGWPAEDLAGYVDGEAHPIELREDGWALRPYQKQAVEGFWHGGSGVVVLPCGAGKTLVGAGAMATAKSTTLILVTNTVSARQWKHELMRRTSLSEEEIGEYSGTRKEIRPITIATYQVLTTKRKGIYPHLELFDSRDWGLIVYDEVHLLPAPVFKFTADLQARRRLGLTATLVREDGRESDVFSLIGPKRFDAPWKEIEAQGYIAPADCVEVRVNLTDSERLTYATAETDEKYRYCATTDSKRIVTEALVARHKGQQTLVIGQYIDQLDELGEHLDAPVIKGETTNAQREKLFDAFREGELSVLVVSKVANFSIDLPEATVAIQVSGTFGSRQEEAQRLGRVLRPKADGHPAIFYSVVARDTIDQDFAAHRQRFLAEQGYAYRIVDASALLADEDV
>NZ_CP023992.1|WP_099016983.1|4441199_4441670_-|VanZ-family-protein
MLVAFVCMVGFAAALAKATLVPSPDSVDLVHTNLHPGRSLRTYIDQPAFRDTVKQIGGNVLLGAPFGVLLPMLVPRARGAVRVAVVTALVMVAVETVQGLIVEGRAFDIDDVILNTTGALLGYVVIGRRLGHALYPRRRHWWHRWTRRGTQPPPAA
>NZ_CP023992.1|WP_099014109.1|4436192_4437479_-|hypothetical-protein
MGIESEKLVYDYLSRVGDLAQQQGLSSGERMRLVSGLRADIDHRRATGGADSPAGVKRILSKLGSPADVVAAAGGRPDPGSGTGGEPGGAESGGTAAGVGGGAAPRGAAGAARAARDKLAGLAKSSGLTGKVPSPREEDAPGVPGVGRNGGRNGSGPSGGVPGDGATSLIKPRPATPATPPPDAASPPHLAGEDELGPRESNMDWWHVEPGPFAQPERSDAQYGAVEGFTGGIEIPELLGKGKSPEQQRQERREAEEKAAAEKAATEAKAAEEAKAKDQAKAEAGAKKRGALRRVLLGPGKAGGEPAAGGGVVKWLAGLGPVLLVAVGLLVAGAGLGNFILIAFGWVIAYYGTYRRSPAEAKWAALGVPGLVAAGAVVWLWGRSDGKWGEPIPKDGWQDVLTDTWPYVVRGAAIASVLFLLWRARRKG
>NZ_CP023992.1|WP_099016982.1|4434946_4435720_+|ABC-transporter-ATP-binding-protein
MTLAYEDRTVVDGLDLEIPDGEVTVIVGPNACGKSTLLRALGRLLRPRGGAVLLDGTDLARIPTKRIARSVGLLPQTPVAPEAITVADLVSRGRQPHQHWWQQWSEEDERAVTDAMERTDVTALADRPVDELSGGQRQRVWIAMALAQETDLLLLDEPTTYLDISHQVEVLDLVRQLNHERGRTVVAVLHDLNQAARYADHLIAMKTGRIVARGRPEDIVTAELVHEVFGLESVVVPDPVTGSPLVVPGTPWRAEKG
>NZ_CP023992.1|WP_069870744.1|4433774_4434860_+|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MSAGHGGGGARGGYGARGGSFLLHRRSALVAIGLTLATAAVCVAYLCVGESFVAPADAVKAVLHTQWGLGPATPNDLVVGTLRLPRMTLGLLVGAAFGIAGALIQTVARNPLASPDIIGVSQGASAVTVGAMTYGIGSFTVLPYLSVAGGLAAAALVYVFAWRGGLHAARFVLIGIGFAVALRSITHLFLTKGDYLVAQQAKVWMTGSLNGRGWGEAAPLGWALLVLLPGVLWAARAQRTVSLDDDTATALGVRLGRVRLGLASLGIVLASMATGAAGPVDFVALLAPQIARRMTRTAQIPLLCSALTGAFIVVTADLLARKLFAPTELPVGVLTAAVGAPYLIHLLLSSGGRGRKGGTAA
>NZ_CP023992.1|WP_099014114.1|4452512_4453859_-|cation/H(+)-antiporter
MGHADTLLALGGAFLAAAVLARLGSRIGLPTIPLFMLAGILLGPHTPGLVLVEDARDFEMLSALGLVLLLFYLGLEFHLDDLRSGGRRLLAAGGIYLLLNVGAGLGFGFALGWGAREALVLAGVLGISSSAIVTKILIDLGRIARPETRLILGVIVVEDIFLALYLAALQPVISGAQGIQETVLQAGKAFGFLLALAVAARYGTRLIGRLISVRDNELLVITFLGTAVLVAGVSEVLGVADAIGAFMAGLILAGTRSGPRIRELVHPLRDAFAAIFFFAFGLAIDPGDIASVAAPVAAAAALTIVMNVIAGLLVARLYRYGPEPAADIATTLLARGEFALVLAAMATSAGLDARLAPFIAGYVLVLAVLGPVVAGRAHLLARVLRSVRTTPPDDRPDPASAAPTPAPDAPGASGPETAGAGSRPMPSAPVSSARVSSAGVSSPGEPER
>NZ_CP023992.1|WP_099014115.1|4454235_4454568_-|DUF3040-domain-containing-protein
MAAPGDIQLHELEERMARSDPRFARGLGEGRPRRPREYRRGPAWVLLAISLAMQVAGMLLPQGLLLAAGLVVAGIAARQFVSPPGRRSDRPWWRLPHSRHGTNGPAPRHG
>NZ_CP023992.1|WP_099014116.1|4454934_4455882_+|sensor-histidine-kinase
MSLFWRIFLLNAVVLIIATALLLGPVTVSTPVLLTEAAVLTGGLGVMLIANGLLLRIGLVPLQRLTRAMTTIDLLRPAQRPAVGGRGEVAELITTFNAMLDRLEAERATSAARALSAQESERHRIAQELHDEVGQSLTAVLLELNRAAGHAPPDLREDLHQVQETTRTSLDEIRRIARRLRPGVLEELGLTSALKALTNEFTGATLVVHHRIAADLPPLEAETELVLYRVAQESLTNVARHAAARRAELALNRGPAGVELRVRDDGRGLGDAAEGAGIRGMRERALLIGAELDLGSAPGGGTDVRLTVPIPHRSQ
>NZ_CP023992.1|WP_079258050.1|4455884_4456544_+|response-regulator-transcription-factor
MPEATETRILLADDHALVRRGVRLILEGEPDLTVVAEAGDGAEAIEAARAHRPDLAILDIAMPRMTGLQAARELARSQPETRILILTMYDNEQYFFEALAAGASGYVLKSVADRDLVEACRATMRGEPFLYPGAVNALIRNYLGRLQEGESIPGRPITSREEEILKLVAEGHSSQQIADLLVISVKTVERHRANLLQKLGLKDRLELTRYAIRVGLIEP
>NZ_CP023992.1|WP_099014117.1|4456595_4456883_-|DUF4031-domain-containing-protein
MAVLIDPPSWPGHGRLWSHLVSDVSFAELHAFAARIGAPRRGFDRDHYDLPSELYAKAVRAGAEEVGSKELLRRLKAAGLRRPKRAADRLGRSGS
>NZ_CP023992.1|WP_093701802.1|4456882_4457239_-|hypothetical-protein
MKLEQALHAARALVLADLAAGEVARADIVSLVEDAIAHRRWWVEQWPEGVAYVAGLVAQDVQDALLERYGRWPLCPVCTQGGDLHALDVEPELGSDPHWVCGKTAVAVARVGSLGTTL
>NZ_CP023992.1|WP_087684229.1|4457529_4458459_+|MurR/RpiR-family-transcriptional-regulator
MPPPQPDATPPIPPTPPAPAALAAKVRTLGPSMTRSMQRVAEAVAGDPAGCAALTVTGLAERTGTSEATVVRTSRLLGYPGYRDLRLALAALAAQQAAGRAPAVTADIAVDDPIADVVTKLAREEQQCLADTAAGLDTSQVEAAVSALAAARRIDVYGVGASSLVGQDLVQKLLRIGLIAHAHADPHLAVTNAVQLHSGDVAIAITHSGRTTDVIEPLRVAFERGATTVAITGRPNGEVAQYADLVLTTSTARESELRPAAMSSRTSQLLVVDCLFIGVAQRTYESAAPALSASYEALAHRHDPRPGHR
>NZ_CP023992.1|WP_099016984.1|4458894_4459836_+|N-acetylmuramic-acid-6-phosphate-etherase
MTTEAFRPELAEIDRLETFEIARIMNAEDAAVPAAVAGELPRIAAAIDAIAARMSRGGRLLYAGAGTAGRLGVLDASECPPTFNTRPEQVVGVIAGGPDAVVTSVEGAEDSEELAARDLERLRIGPDDTVVGVSASGRTPYAVGAVRYARRCGALTVGLSCNADSALAAAADHGIEIVVGPELLTGSTRLKAGTAQKLVLNMISTITMIRLGKTFGNLMVDVRASNDKLRARSRRIVFLATGASEQRIESALAATDGEVKNAILTILGGVDAPTAEKLLAEAHGHLRTALDAATGPTGPTGPTDSTGPTGYTG
>NZ_CP023992.1|WP_069870626.1|4459957_4461583_-|chaperonin-GroEL
MAKIIAFDEEARRGLERGMNQLADAVKVTLGPKGRNVVLEKKWGAPTITNDGVSIAKEIELEDAYEKIGAELVKEVAKKTDDVAGDGTTTATVLAQALVKEGLRNVAAGANPMALKRGIEKAVEAVSAQLLEQAKDVETKEQIASTASISAADTQIGELIAEAMDKVGKEGVITVEESQTFGLELELTEGMRFDKGYISPYFATDMERMEASLDDPYILIVNSKISSVKDLLPLLEKVMQSGKPLLIIAEDVEGEALATLVVNKIRGTFKSVAVKAPGFGDRRKAMLGDIAILTGGTVISEEVGLKLENAGLDLLGRARKVTVTKDETTIVDGAGDTEQVQGRVNQIRAEIESSDSDYDREKLQERLAKLAGGVAVIKAGAATEVELKERKHRIEDAVRNAKAAVEEGIVAGGGVALLQTVSVFEKLELDGDEATGAQAVRLALEAPLKQIAVNAGLEGGVVVEKVRNLTPGHGLNAATGEYVDLIAEGIIDPAKVTRSALQNAASIAALFLTTEAVIADKPEKAAPAGAPGGMPGGDMDF
>NZ_CP023992.1|WP_009716982.1|4461922_4462129_-|cold-shock-protein
MAQGTVKWFNAEKGYGFIAVDGGADVFVHYSAIQMDGYRTLEEGQRVEFEISQGQKGPQADMVRVAVG

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Crispr_ID: NZ_CP023992_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_10

4521525-4521635

Orphan

Consensus_repeat	Method
CGGGTGGCAGCGCGCCCGCGGTCGGGGCGG	CRISPRCasFinder

1 spacers

csa3

The CRISPR arrays of NZ_CP023992_10

>merge|NZ_CP023992|10|4521525-4521635|CRISPRCasFinder
CGGGTGGCAGCGCGCCCGCGGTCGGGGCGGCCCCCGGTCTCGCGGTCGGTGACGCCTCCGATGGCTAGGTGGACAGCGGCCCGGGTGGCAGCGCGCCCGCGGTCGGGGCGG

>NZ_CP023992|10|10|4521525-4521635|CRISPRCasFinder
CGGGTGGCAGCGCGCCCGCGGTCGGGGCGG	CCCCCGGTCTCGCGGTCGGTGACGCCTCCGATGGCTAGGTGGACAGCGGCC
CGGGTGGCAGCGCGCCCGCGGTCGGGGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069860843.1\|4519136_4519898_-\|phosphoglyceromutase	unknown	unknown	gnl\|CDD\|184519
NZ_CP023992.1\|WP_099014138.1\|4514189_4514957_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP023992.1\|WP_099014143.1\|4517610_4518156_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|198381
NZ_CP023992.1\|WP_099014151.1\|4532801_4533827_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381313
NZ_CP023992.1\|WP_099014149.1\|4527046_4527568_-\|YbjN-domain-containing-protein	unknown	unknown	gnl\|CDD\|371210
NZ_CP023992.1\|WP_099014140.1\|4515405_4515696_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014150.1\|4527560_4528922_-\|D-inositol-3-phosphate-glycosyltransferase	unknown	unknown	gnl\|CDD\|132490
NZ_CP023992.1\|WP_099014148.1\|4525149_4526889_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378931
NZ_CP023992.1\|WP_142881413.1\|4524743_4524998_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014139.1\|4515008_4515371_+\|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|223713
NZ_CP023992.1\|WP_099014141.1\|4515692_4516097_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023992.1\|WP_069860840.1\|4516255_4516801_+\|UTRA-domain-containing-protein	unknown	unknown	gnl\|CDD\|214869
NZ_CP023992.1\|WP_099014142.1\|4516797_4517580_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225099
NZ_CP023992.1\|WP_079258079.1\|4529063_4529876_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014137.1\|4513214_4514000_-\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225099
NZ_CP023992.1\|WP_093699731.1\|4536501_4537311_+\|deaminated-glutathione-amidase	unknown	unknown	gnl\|CDD\|143605
NZ_CP023992.1\|WP_079258081.1\|4535423_4536398_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|270229
NZ_CP023992.1\|WP_079152803.1\|4533844_4535242_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|185378
NZ_CP023992.1\|WP_099014146.1\|4521694_4523767_-\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|320687
NZ_CP023992.1\|WP_099014144.1\|4518365_4519055_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069860843.1\|4519136_4519898_-\|phosphoglyceromutase	gnl\|CDD\|184519	PRK14120, gpmA, phosphoglyceromutase; Provisional.	0
NZ_CP023992.1\|WP_099014138.1\|4514189_4514957_-\|SDR-family-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. 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 prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, 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.	7.97077e-72
NZ_CP023992.1\|WP_099014143.1\|4517610_4518156_-\|hypothetical-protein	gnl\|CDD\|198381	cd10434, GIY-YIG_UvrC_Cho, Catalytic GIY-YIG domain of nucleotide excision repair endonucleases UvrC, Cho, and similar proteins. UvrC is essential for nucleotide excision repair (NER). The N-terminal catalytic GIY-YIG domain of UvrC (also known as Uri domain) is responsible for the 3' incision reaction and the C-terminal half of UvrC, consisting of an UvrB-binding domain (UvrBb), EndoV-like nuclease domain and a helix-hairpin-helix (HhH) DNA-binding domain, contains the residues involved in 5' incision. The N- and C-terminal regions are joined by a common Cys-rich domain containing four conserved Cys residues. Besides UvrC, protein Cho (UvrC homolog) serves as a second endonuclease in E. coli NER. Cho contains GIY-YIG motif followed by a Cys-rich region and shares sequence homology with the N-terminal half of UvrC. It is capable of incising the DNA at the 3' side of a lesion in the presence of the UvrA and UvrB proteins during NER. The C-terminal half of Cho is a unique uncharacterized domain, which is distinct from that of UvrC. Moreover, unlike UvrC, Cho does not require the UvrC-binding domain of UvrB for the 3' incision reaction, which might cause the shift in incision position and the difference in incision efficiencies between Cho and UvrC on different damaged substrates. Due to this, the range of NER in E. coli can be broadened by combining action of Cho and UvrC. This family also includes many uncharacterized epsilon proofreading subunits of DNA polymerase III, which have an additional N-terminal ExoIII domain and a 3'-5' exonuclease domain homolog, fused to an UvrC-like region or a Cho-like region. The UvrC-like region includes a GIY-YIG motif, followed by a Cys-rich region, and an UvrB-binding domain (UvrBb), but lacks the EndoV-like nuclease domain and the helix-hairpin-helix (HhH) DNA-binding domain. The Cho-like region consists of a GIY-YIG motif, followed by the Cys-rich region, and the unique uncharacterized domain presenting in the C-terminal half of Cho. Some family members may not carry the Cys-rich region. This family also includes a specific Cho-like protein from G. violaceus, which possesses only UvrBb domain at the C-terminus, but lacks the additional N-terminal ExoIII domain. The oother two remote homologs of UvrC, Bacillus-I and -II, are included in this family as well. Both of them contain a GIY-YIG domain, but no Cys-rich region. Moreover, the whole C-terminal region of Bacillus-I is replaces by an unknown domain, and Bacillus-II possesses another unknown N-terminal extension.	0.00141585
NZ_CP023992.1\|WP_099014151.1\|4532801_4533827_+\|aldo/keto-reductase	gnl\|CDD\|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	9.86706e-150
NZ_CP023992.1\|WP_099014149.1\|4527046_4527568_-\|YbjN-domain-containing-protein	gnl\|CDD\|371210	pfam10722, YbjN, Putative bacterial sensory transduction regulator. YbjN is a putative sensory transduction regulator protein found in Proteobacteria. As it is a multi-copy suppressor of the coenzyme A-associated temperature sensitivity in temperature-sensitive mutant strains of Escherichia coli the suggestion is that it both helps CoA-A1 and possibly works as a general stabilizer for some other unstable proteins. This family was expanded to subsume other related families: DUF1790, DUF1821 and DUF2596.	9.55811e-20
NZ_CP023992.1\|WP_099014150.1\|4527560_4528922_-\|D-inositol-3-phosphate-glycosyltransferase	gnl\|CDD\|132490	TIGR03449, mycothiol_MshA, D-inositol-3-phosphate glycosyltransferase. Members of this protein family, found exclusively in the Actinobacteria, are MshA, the glycosyltransferase of mycothiol biosynthesis. Mycothiol replaces glutathione in these species.	0
NZ_CP023992.1\|WP_099014148.1\|4525149_4526889_-\|hypothetical-protein	gnl\|CDD\|378931	pfam12708, Pectate_lyase_3, Pectate lyase superfamily protein. This family of proteins possesses a beta helical structure like Pectate lyase. This family is most closely related to glycosyl hydrolase family 28.	4.94262e-19
NZ_CP023992.1\|WP_079258081.1\|4535423_4536398_+\|hypothetical-protein	gnl\|CDD\|270229	cd01008, PBP2_NrtA_SsuA_CpmA_like, Substrate binding domain of ABC-type nitrate/sulfonate/bicarbonate transporters, a member of the type 2 periplasmic binding fold superfamily. This family represents the periplasmic binding proteins involved in nitrate, alkanesulfonate, and bicarbonate transport. These domains are found in eubacterial perisplamic-binding proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates. Other closest homologs involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB) are also included in this family. After binding their ligand with high affinity, they interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. These binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.81664e-07
NZ_CP023992.1\|WP_099014139.1\|4515008_4515371_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|223713	COG0640, ArsR, Predicted transcriptional regulators [Transcription].	1.45927e-09
NZ_CP023992.1\|WP_099014141.1\|4515692_4516097_-\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.16468e-19
NZ_CP023992.1\|WP_069860840.1\|4516255_4516801_+\|UTRA-domain-containing-protein	gnl\|CDD\|214869	smart00866, UTRA, The UbiC transcription regulator-associated (UTRA) domain is a conserved ligand-binding domain. It has a similar fold to HutC/FarR-like bacterial transcription factors of the GntR family. It is believed to modulate activity of bacterial transcription factors in response to binding small molecules.	1.23419e-23
NZ_CP023992.1\|WP_099014142.1\|4516797_4517580_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	4.57295e-35
NZ_CP023992.1\|WP_099014137.1\|4513214_4514000_-\|GntR-family-transcriptional-regulator	gnl\|CDD\|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	7.59706e-41
NZ_CP023992.1\|WP_093699731.1\|4536501_4537311_+\|deaminated-glutathione-amidase	gnl\|CDD\|143605	cd07581, nitrilase_3, Uncharacterized subgroup of the nitrilase superfamily (putative class 13 nitrilases). The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13). Class 13 represents proteins that at the time were difficult to place in a distinct similarity group; this subgroup represents either a new class or one that was included previously in class 13. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	1.27367e-122
NZ_CP023992.1\|WP_079152803.1\|4533844_4535242_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|185378	PRK15481, PRK15481, transcriptional regulatory protein PtsJ; Provisional.	5.72301e-61
NZ_CP023992.1\|WP_099014146.1\|4521694_4523767_-\|M48-family-metalloprotease	gnl\|CDD\|320687	cd07328, M48_Ste24p_like, M48 Ste24 endopeptidase-like, integral membrane metallopeptidase. This family contains peptidase M48-like proteins that are as yet uncharacterized, but probably function as intracellular, membrane-associated zinc metalloproteases; they all contain the HEXXH Zn-binding motif, which is critical for Ste24p activity. They likely remove the C-terminal three residues of farnesylated proteins proteolytically and are possibly associated with the endoplasmic reticulum and golgi.	1.45101e-32

>NZ_CP023992.1|WP_069860843.1|4519136_4519898_-|phosphoglyceromutase
MADAPYKLILLRHGESEWNAKNLFTGWVDVNLNEKGEKEAVRGGELLKDAGLLPDVLHTSLLKRAIRTSQLALDAADRLWIPVRRSWRLNERHYGALQGKDKAQTLAEFGEEQFMLWRRSYDTPPPPLEDGAEWSQSDDPRYATIPPELRPRTECLKDVVERMLPYWYDGIVPDLLAGHTVLVAAHGNSLRALVKHLDGISDADIAGLNIPTGIPLSYDLDTDFRPVTPGGTYLDPDAAKAAIEAVKNQGKKK
>NZ_CP023992.1|WP_099014144.1|4518365_4519055_+|hypothetical-protein
MMEQLQKLVDRHRDCRQESVRFRPSTWRPRLEPYGAAHVLDVGVGCVSPSGDRLISRGDLVDLRDRVGDDPDGLRDLFVAVMIWGSGTTNGRGPRYTEAALSDARLPAVLRTTRQAVRSGDLSGAYRQFILNGVRRSFSTKWFAAVDDRDVGCARALILDSRVLHSLNALGWSSWQAAGTRRWPTRYATYVSSMHGWASSLGVTADWLEWLLFHLNGRVDGPREGQDST
>NZ_CP023992.1|WP_099014143.1|4517610_4518156_-|hypothetical-protein
MEATALTSPDRLWSGQEVLTRPSPVPAVPGVYGWHFEQPPHPDLDARCLLYVGIAPRYMANRTSTQNLRKRVRYHYRGNAAGSTLRLTLGCLLGLELRRVGSGKRMTFGKAGEATLSQWMADNARVCWVERGEPWALESQLISQLDLPLNLAQNGHNAFHSRLKELRAQARQRARELSISA
>NZ_CP023992.1|WP_099014142.1|4516797_4517580_+|GntR-family-transcriptional-regulator
MTVPKAEQDAVDRRSLHERIAADLRDEIMSGDLPPGAKLPSTAQLKERFTASNATVQKALQLLKDEGLAVGRAGAAVTVREHRQRTMRPASYMAPAAPGEPYRWISEAAAEHQARGTSRLLDVTEIRPPSDVAEALRLPEDGTALLRAQVLLLDDEPVELVKSYYPLELARGTAMMDRRKIKGGTPALLAELGYPPRLSVDKVSARVPTQEQYTLLDLPGNLPVLRTLRVVYSDGERPIEATVMAKAGHLYELQYEFTPA
>NZ_CP023992.1|WP_069860840.1|4516255_4516801_+|UTRA-domain-containing-protein
MASDAWISSSMPYLRPVEAGGQGDAWGEEAAARGRRGTQRILHAGEVSAPAAVARLLGLENGDTVVVRRRIMYLDEEPCELTDSYYPAHIAAGTGLAGTAKIRGGAVGLLAELGHVGQRVREDVTARLPDARERELLRTGAEEPVLCLERVVLDEDKRPIQADLITMPAQRQRLRYELRMG
>NZ_CP023992.1|WP_099014141.1|4515692_4516097_-|ATP-binding-protein
MPLMRQQSFTRRKPSIRATRQFVSRTLSEWGYVDRLEEIQLCVSEIATNALLHGVPPGRLFRVRIEAAEEEVRIEVRDSGPGRPTAQSPRADSENGRDLLLVGELADAWGNVEHTVGKTVWFVVKATQTQGRAQ
>NZ_CP023992.1|WP_099014140.1|4515405_4515696_-|hypothetical-protein
MTVRRGHAHGRDFDQLHRDEITVAMNWVIRICQDVVRDHSHMTFWVPTGTPTGAAPTMDHLIDSARTDVLNKLRRQIDGAEAIIGNAEHERAKRQR
>NZ_CP023992.1|WP_099014139.1|4515008_4515371_+|helix-turn-helix-transcriptional-regulator
MASVKQARHPATDEITLIDVMGALNDPIRVGLIRVLADDREHGWGELRAPVAKSTLSHHLRVLRDAGVTRTRQEGTRCFVKLRSDDLNARFPGLLTAILDAAHHDDVGSHVGLADDSPTA
>NZ_CP023992.1|WP_099014138.1|4514189_4514957_-|SDR-family-oxidoreductase
MSVKPPADDLAERVVIVTGAGSGIGRAAARAFARAGARVLGVGRRIDALQETAAGQPAIVAYSADLSDPGAPGEVVNAAVDRWGQLDVLVNNAGITKIMPLADTTDTGITDLFGLNVVAPSLLAREALPHLRRSRGSIVNISSTYGHRPMPGGAHYAASKAALEQLTRSWAVELAADGIRVNALAPGPTESQALAAAGLPDEAIEQIKREEASRIPLGRRGDPDEVAAWILRLADPATTWLTGQILTVDGGLELT
>NZ_CP023992.1|WP_099014137.1|4513214_4514000_-|GntR-family-transcriptional-regulator
MAKYEQIADALRQGIRAGQLGPGERLPAEDKLAARYRTSVPTLQRALSELVAEGLIDRRHGVGTFVRTPRRRVERSNDRHQWEKDRARRSRAERLRTGSTEHDTGLEVTDLAFHAEYRDAKADEDLASVFRIPVGTRLLERIYRTNCLEEDAPFALVNSYLVHDVVAVNPELLDAANEPWPGGTQNQLYTIGIELDRIAERITARPPTVEEAEGLGLKKGVSVIVLRKICTDIGGRVVEVSDVTLCGDRTELVFTTPLKRW
>NZ_CP023992.1|WP_099014146.1|4521694_4523767_-|M48-family-metalloprotease
MIAAARAVLALALLAVFYALVAAMVLLWAAFLAAALWTAGAPGVQTPPMSVITACAAFAPIVFGMVWAVIRTARPAAAREDAVTVTRRGAPELWDTVEELALDIGTRPPGHIRLTAEANASVTEDAPLLGLAPGRRVLYLGLPLLAGLSRAELRAVLAHELGHFSRRHSRFGVVAHRGAAGLVAARQAIQDAAAANDLVRLYAGGPLLLLNLYTYVFRWLTRPVRRRQELEADREAARVAGPDAVADALRSTTALDAAWQEFLAEFLAPMRRATGRIPDDPFRAFAHMVEAPELREPLAALRARAVERPADPDDAHPALATRLERLARLPAAEPGTASLSLDPFSLDPLALRPRYAVALGRVMLPGPDAGTRVPWRDWLTELAEHRATRILPPLAEAAREVEETEGMGRKKANPEPKPEPGKEPGPESVTGSVTAPATEPDALTVQRVLWLLDSGRRMPLARALNSRLPHGERMFHGERTELDPLGPLAEALAVLIGAQLVAKGTAYWAMNWTGPSILVPPDGIAPETIRTWADTAVRLPGQTRQLGLHLAALGVDERAPLPSTDPAGDTADGPAPAGKARQISITPGITGPARRRIKAVGGLALTVLLLMTGLSLALWANSDDPSYPRVPVTRWTDRYQPGGGTGTEPAPFPTYQQPTFPARPTIPTFQLPPRSVPTIRIEPVIPRPAP
>NZ_CP023992.1|WP_142881413.1|4524743_4524998_-|hypothetical-protein
MDNPWLTVATVVTVGVLRLMGDVIRWLAARSGERLRARTLAELVSRTEPGTVLTDRRPDGAALTIWRDTDRTVASGGAGRGRSA
>NZ_CP023992.1|WP_099014148.1|4525149_4526889_-|hypothetical-protein
MGMEIGRRRLLGGAMGLAAGATALGAGAPLLTATDAAAAPRTAGGTGGAGGTGDPGGARTSPLWQEFLDRPYTHPQLPYVGRAGYLGGRTSFPRPPVVADVRDYGARPDGSADAAPAINRAIEAAGRRGGGTVLVPPGTYRVDDVIRLGYDNVVLRGAGSGRTTLHATRNLTELIGPYGSRYGGDKSSWSWAGGLIWICPDARLRSLTDAIRARAWPFEGWTGNRRDEWRTLTGLAAPARRGDWTVTVEDPSALRPGDRVLLQLADDDTHSLLSHMAGDVEGAADYVWTDKTKLTSYVPYEWPCRVAAVDRGRGRVTLDRPLPLDARPAWRPRFTTLVPPVTGSGVEGITLDVVETPQAQHLLDKGYNGVALQCAWDCWVDDVTVNNVDNGFLLVAAKACTLRRTRVTGRGSHHPYCCREGSHDNLVEDFVLARRTVPAPAGTQLHGINVEGLSSYNVWSRGRMEMGTFDTHRGMPFANVRTEITVDNTGSHGGDASAGPLYGARFAHWNVTVTNERAGCVRIDDIAPYSATVGISEVRQFGQIDVPDFTGPLHSRIESYGHPEAVQPRNLYQAQRALR
>NZ_CP023992.1|WP_099014149.1|4527046_4527568_-|YbjN-domain-containing-protein
MADPMADTAPEADLRAVIERTLNDAELEWESPEDGTYVVTLPGTRKLSTTCSLRVGRHSLSVNAFVVRHPDENHAAVHRWLLERNTRLYGVSYAIDQLGDIYLVGKLPLAAVTPEELDRLLGTVLENADGSFNTLLEMGFATAIRKEYAWRTSRGESTRNLEAFSNLTRDAAK
>NZ_CP023992.1|WP_099014150.1|4527560_4528922_-|D-inositol-3-phosphate-glycosyltransferase
MSQHASRLGGLRGRSHVPFGTPSHQRLRRMPRRPRRIAMLSVHTSPLHQPGTGDAGGMNVYIVELAKRLAAIDIEVEIFTRATTAALPPAVELAPGVLVRHVDAGPYEGLAKEDLPAQLCAFTHGVMQAWAGHRPGHYDLVHSHYWLSGHVGWLAAERWGVPLVHAMHTMAKVKNAALAEGDTPEPAARVIGEQQIVRAADRLIANTDEEAEELARHYEAARELVAVVHPGVNLDRFRPADGRAAARARLGLPADALIPLFAGRIQPLKAPDILLHAVAHLLEEDPSLRERIVVPVVGGPSGSGLAKPEGLHKLAARLGICDVVRFRPPCAQDELADWYRAASVLVMPSYSESFGLVAIEAQACGTPVVAASVGGLPVAVRDGVSGTLIHGHDPADYARALRPFAAEPERADRMGAAAARHAESFGWDTAAAATAEVYTEAMRERRRLRSGHG
>NZ_CP023992.1|WP_079258079.1|4529063_4529876_+|class-I-SAM-dependent-methyltransferase
MPARVPPPSRPIGSATRGTTNPNRLRRMDRWIAAAHGAALRRAGEPPVAVDLGYGAAPWTAVELLDRLRTVRGGTRVVGVEIDPGRVAAARPYEREGLTFAHGGFEVPLPGGARPALIRAANVLRQYEEGEVAAVWRRLCARLAPGGLLVEGTCDEIGRRHVWVALGPAGPRTVTFAARLGSLERPSDLAERLPKALIHRNVPGEPVHTFLRDFDRAWAAAAPYAPLSARQRWIRSAQTLRAAGWPLADGPRRWRQGEVTVRWEALAPRG
>NZ_CP023992.1|WP_099014151.1|4532801_4533827_+|aldo/keto-reductase
MKRRILGGTGISVSEYALGAMMFGALGNPDHDDSVRIIHRALDAGINFVDTADVYSAGESEEIVGKALKGRRDDIVLATKARSSMGDDPNHGGSSRRWITREVENSLRRLGTDHIDLYQIHRPDPATDVDETLSVLSDLVRAGKVRAVGSSTFPAEQIVEAQWVSDRRGHVRFRSEQPPYSILARGVEAAVLPTAQKYGMGVLSWGPLSAGWLTGRYTKAADVDLSGGRAAVEKHKFDPSLPGNARKLEAVGALSELASDAGLPLAHLAVAFVRAHPAITSVIIGPRTMEQLEDLLAGSEVELSEDVLDRIDEIVPPGTDLNPADSYYTPPALGDKRLRRR
>NZ_CP023992.1|WP_079152803.1|4533844_4535242_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MQENTADPAVARPGDPASVAGLAARIPDTSARGIAAAMTDLIRAGELAPGSALPTVRALAAGLGVSPGTVAEAWAVLRKHRMIATLGRRGSVVSGPPTVPHPTRYERVGDFGDHLALDLAVAAPDPALLPPLESALLAGARTPRLNDYARTAITDGLLAAVADSWPYRPDAWMAVGGGYEGVQLLCQALLVPGDRVAVEDPTAARLLDILEALDAQTVPVACDDQGPLPDSLARALTARPALFLHQSRAQVPCGWSLGPERAAALAGVLEGAPNVAILEDDGLGPLTTGPVAVLGAHLPHRTALVRSYSKAYGPDLRIAVVGGPREMVERARVLRTFGTGWTSRILQDALAHLLTDEDAGRCVREAARHYDARRSALAERLAERGVHTANRDGLMLWVPVVDETSALVTLAARGITVSPGSRFCVSYARPHVRVATSRLTRDGAALDQIAELIALAASSSAGRME
>NZ_CP023992.1|WP_079258081.1|4535423_4536398_+|hypothetical-protein
MSSPVIRLGLRDWDHLVPLASGLVEIPGFTVRVDARDVTPDVLTEPGLDGGETSFSRYVQARAAGDDRLVGLPAFVMRGFRHRCVLVREDSPLRSLGQLAGARIGLTGWPDSGNTWTRALLRAAGVDLAGVRWLVGPLTADETGKDRVGGRPLPAGVSVMAEGESLVDELAAGRLDAVLSPFMPRELFTRTSRFRHLLDDHRTEERAYWEATGFVPGIHLVTLKREVVEAHPELPAALLAGLEESKRRWLGRRRLLADTTPWLLHELTESARLFGDDWMPYGTKSNAEMTRAFCEELYAQGVWPEPIDPEVVFPDPALAAVPAL
>NZ_CP023992.1|WP_093699731.1|4536501_4537311_+|deaminated-glutathione-amidase
MRIAVGQFAATPDWKDNLAACQELTAQAVRGGADLLVLPEGVLARFTEDRHRIREVAQPLDGPFVSEMLAATAGSATTVVVGIHEPSEDGRVFNTLVALRDGELIARYRKIHLYDAFGDLESANVRPADEPPVVIDVAGTKVGLMTCYDVRFPELARLLVDAGAEVLALPAAWVRGPAKERHWEVMITARALENTCWVAASGECGPRNIGNSLVVDPLGTVRSRLAAAPGLAWADAAPDTTAAARRTLPVLANRRFAVDPTVIPLGAPQ

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Crispr_ID: NZ_CP023992_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_11

4536377-4536450

Orphan

Consensus_repeat	Method
CGCCGCCGTCCCCGCACGCCGACCC	CRISPRCasFinder

1 spacers

PD-DExK

The CRISPR arrays of NZ_CP023992_11

>merge|NZ_CP023992|11|4536377-4536450|CRISPRCasFinder
CGCCGCCGTCCCCGCTCTCTGAGCCCCGCCCTACGCCGCCGTCCCCGCACGCCGACCCCCGCTCCCGCCGCCCT

>NZ_CP023992|11|11|4536377-4536450|CRISPRCasFinder
CGCCGCCGTCCCCGCTCTCTGAGCC	CCGCCCTACGCCGCCGTCCCCGCA
CGCCGACCCCCGCTCCCGCCGCCCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069860843.1\|4519136_4519898_-\|phosphoglyceromutase	unknown	unknown	gnl\|CDD\|184519
NZ_CP023992.1\|WP_099014152.1\|4537319_4538255_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270225
NZ_CP023992.1\|WP_099014145.1\|4520041_4521592_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340887
NZ_CP023992.1\|WP_079152803.1\|4533844_4535242_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|185378
NZ_CP023992.1\|WP_099014151.1\|4532801_4533827_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381313
NZ_CP023992.1\|WP_099014149.1\|4527046_4527568_-\|YbjN-domain-containing-protein	unknown	unknown	gnl\|CDD\|371210
NZ_CP023992.1\|WP_099014154.1\|4540177_4540627_-\|NUDIX-hydrolase	unknown	unknown	gnl\|CDD\|239645
NZ_CP023992.1\|WP_079258079.1\|4529063_4529876_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014148.1\|4525149_4526889_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378931
NZ_CP023992.1\|WP_142881413.1\|4524743_4524998_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014150.1\|4527560_4528922_-\|D-inositol-3-phosphate-glycosyltransferase	unknown	unknown	gnl\|CDD\|132490
NZ_CP023992.1\|WP_099016988.1\|4546022_4547090_-\|DUF1016-domain-containing-protein	PD-DExK	COG4804_PD-DExK_CAS-I:CAS-III	gnl\|CDD\|377634
NZ_CP023992.1\|WP_099014153.1\|4538279_4539299_+\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP023992.1\|WP_093699731.1\|4536501_4537311_+\|deaminated-glutathione-amidase	unknown	unknown	gnl\|CDD\|143605
NZ_CP023992.1\|WP_069860855.1\|4542385_4544641_-\|RNA-degradosome-polyphosphate-kinase	unknown	unknown	gnl\|CDD\|235469
NZ_CP023992.1\|WP_099016987.1\|4540734_4542369_-\|CHAD-domain-containing-protein	unknown	unknown	gnl\|CDD\|237171
NZ_CP023992.1\|WP_099014156.1\|4547277_4549098_+\|bifunctional-metallophosphatase/5'-nucleotidase	unknown	unknown	gnl\|CDD\|277357
NZ_CP023992.1\|WP_099014146.1\|4521694_4523767_-\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|320687
NZ_CP023992.1\|WP_079152843.1\|4539355_4540108_+\|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224051
NZ_CP023992.1\|WP_099014155.1\|4545027_4545960_-\|mycothiol-synthase	unknown	unknown	gnl\|CDD\|132489

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069860843.1\|4519136_4519898_-\|phosphoglyceromutase	gnl\|CDD\|184519	PRK14120, gpmA, phosphoglyceromutase; Provisional.	0
NZ_CP023992.1\|WP_099014152.1\|4537319_4538255_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|270225	cd01004, PBP2_MidA_like, Mimosine binding domain of ABC-type transporter MidA and similar proteins; the type 2 periplasmic binding protein fold. This subgroup includes the periplasmic binding component of ABC transporter involved in uptake of mimosine MidA and its similar proteins. This periplasmic binding domain belongs to the type 2 periplasmic-binding fold protein (PBP2) superfamily, whose members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. PBP2 typically comprises 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. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.18504e-76
NZ_CP023992.1\|WP_099014146.1\|4521694_4523767_-\|M48-family-metalloprotease	gnl\|CDD\|320687	cd07328, M48_Ste24p_like, M48 Ste24 endopeptidase-like, integral membrane metallopeptidase. This family contains peptidase M48-like proteins that are as yet uncharacterized, but probably function as intracellular, membrane-associated zinc metalloproteases; they all contain the HEXXH Zn-binding motif, which is critical for Ste24p activity. They likely remove the C-terminal three residues of farnesylated proteins proteolytically and are possibly associated with the endoplasmic reticulum and golgi.	1.45101e-32
NZ_CP023992.1\|WP_079152803.1\|4533844_4535242_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|185378	PRK15481, PRK15481, transcriptional regulatory protein PtsJ; Provisional.	5.72301e-61
NZ_CP023992.1\|WP_099014151.1\|4532801_4533827_+\|aldo/keto-reductase	gnl\|CDD\|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	9.86706e-150
NZ_CP023992.1\|WP_099014149.1\|4527046_4527568_-\|YbjN-domain-containing-protein	gnl\|CDD\|371210	pfam10722, YbjN, Putative bacterial sensory transduction regulator. YbjN is a putative sensory transduction regulator protein found in Proteobacteria. As it is a multi-copy suppressor of the coenzyme A-associated temperature sensitivity in temperature-sensitive mutant strains of Escherichia coli the suggestion is that it both helps CoA-A1 and possibly works as a general stabilizer for some other unstable proteins. This family was expanded to subsume other related families: DUF1790, DUF1821 and DUF2596.	9.55811e-20
NZ_CP023992.1\|WP_099014154.1\|4540177_4540627_-\|NUDIX-hydrolase	gnl\|CDD\|239645	cd03673, Ap6A_hydrolase, Diadenosine hexaphosphate (Ap6A) hydrolase is a member of the Nudix hydrolase superfamily. Ap6A hydrolase specifically hydrolyzes diadenosine polyphosphates, but not ATP or diadenosine triphosphate, and it generates ATP as the product. Ap6A, the most preferred substrate, hydrolyzes to produce two ATP molecules, which is a novel hydrolysis mode for Ap6A. These results indicate that Ap6A hydrolase is a diadenosine polyphosphate hydrolase. It requires the presence of a divalent cation, such as Mn2+, Mg2+, Zn2+, and Co2+, for activity. Members of the Nudix superfamily are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site.	8.08997e-42
NZ_CP023992.1\|WP_099014148.1\|4525149_4526889_-\|hypothetical-protein	gnl\|CDD\|378931	pfam12708, Pectate_lyase_3, Pectate lyase superfamily protein. This family of proteins possesses a beta helical structure like Pectate lyase. This family is most closely related to glycosyl hydrolase family 28.	4.94262e-19
NZ_CP023992.1\|WP_099016988.1\|4546022_4547090_-\|DUF1016-domain-containing-protein	gnl\|CDD\|377634	pfam06250, DUF1016, Protein of unknown function (DUF1016). Family of uncharacterized proteins found in viruses, archaea and bacteria.	5.11975e-74
NZ_CP023992.1\|WP_099014150.1\|4527560_4528922_-\|D-inositol-3-phosphate-glycosyltransferase	gnl\|CDD\|132490	TIGR03449, mycothiol_MshA, D-inositol-3-phosphate glycosyltransferase. Members of this protein family, found exclusively in the Actinobacteria, are MshA, the glycosyltransferase of mycothiol biosynthesis. Mycothiol replaces glutathione in these species.	0
NZ_CP023992.1\|WP_099014153.1\|4538279_4539299_+\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	6.1586e-75
NZ_CP023992.1\|WP_093699731.1\|4536501_4537311_+\|deaminated-glutathione-amidase	gnl\|CDD\|143605	cd07581, nitrilase_3, Uncharacterized subgroup of the nitrilase superfamily (putative class 13 nitrilases). The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13). Class 13 represents proteins that at the time were difficult to place in a distinct similarity group; this subgroup represents either a new class or one that was included previously in class 13. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	1.27367e-122
NZ_CP023992.1\|WP_069860855.1\|4542385_4544641_-\|RNA-degradosome-polyphosphate-kinase	gnl\|CDD\|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP023992.1\|WP_099016987.1\|4540734_4542369_-\|CHAD-domain-containing-protein	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	1.21554e-07
NZ_CP023992.1\|WP_099014156.1\|4547277_4549098_+\|bifunctional-metallophosphatase/5'-nucleotidase	gnl\|CDD\|277357	cd07412, MPP_YhcR_N, Bacillus subtilis YhcR endonuclease and related proteins, N-terminal metallophosphatase domain. YhcR is a Bacillus subtilis sugar-nonspecific endonuclease. It cleaves endonucleolytically to yield nucleotide 3'-monophosphate products, similar to Staphylococcus aureus micrococcal nuclease. YhcR appears to be located in the cell wall, and is thought to be a substrate for a Bacillus subtilis sortase. YhcR is the major calcium-activated nuclease of B. subtilis. The N-terminal metallophosphatase domain belongs to a large superfamily of distantly related metallophosphatases (MPPs) that includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	1.07992e-133
NZ_CP023992.1\|WP_099014145.1\|4520041_4521592_+\|MFS-transporter	gnl\|CDD\|340887	cd17329, MFS_MdtH_MDR_like, Multidrug resistance protein MdtH and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of Escherichia coli MdtH and similar multidrug resistance (MDR) transporters from bacteria and archaea, many of which remain uncharacterized. 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. MdtH confers resistance to norfloxacin and enoxacin. MdtH-like MDR transporters belong 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.	2.24332e-82
NZ_CP023992.1\|WP_079152843.1\|4539355_4540108_+\|amino-acid-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	8.92225e-153
NZ_CP023992.1\|WP_099014155.1\|4545027_4545960_-\|mycothiol-synthase	gnl\|CDD\|132489	TIGR03448, mycothiol_MshD, mycothiol synthase. Members of this family are MshD, the acetyltransferase that catalyzes the final step of mycothiol biosynthesis in various members of the Actinomyctes, Mycothiol replaces glutathione in these species. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	3.70088e-125

>NZ_CP023992.1|WP_079152803.1|4533844_4535242_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MQENTADPAVARPGDPASVAGLAARIPDTSARGIAAAMTDLIRAGELAPGSALPTVRALAAGLGVSPGTVAEAWAVLRKHRMIATLGRRGSVVSGPPTVPHPTRYERVGDFGDHLALDLAVAAPDPALLPPLESALLAGARTPRLNDYARTAITDGLLAAVADSWPYRPDAWMAVGGGYEGVQLLCQALLVPGDRVAVEDPTAARLLDILEALDAQTVPVACDDQGPLPDSLARALTARPALFLHQSRAQVPCGWSLGPERAAALAGVLEGAPNVAILEDDGLGPLTTGPVAVLGAHLPHRTALVRSYSKAYGPDLRIAVVGGPREMVERARVLRTFGTGWTSRILQDALAHLLTDEDAGRCVREAARHYDARRSALAERLAERGVHTANRDGLMLWVPVVDETSALVTLAARGITVSPGSRFCVSYARPHVRVATSRLTRDGAALDQIAELIALAASSSAGRME
>NZ_CP023992.1|WP_099014151.1|4532801_4533827_+|aldo/keto-reductase
MKRRILGGTGISVSEYALGAMMFGALGNPDHDDSVRIIHRALDAGINFVDTADVYSAGESEEIVGKALKGRRDDIVLATKARSSMGDDPNHGGSSRRWITREVENSLRRLGTDHIDLYQIHRPDPATDVDETLSVLSDLVRAGKVRAVGSSTFPAEQIVEAQWVSDRRGHVRFRSEQPPYSILARGVEAAVLPTAQKYGMGVLSWGPLSAGWLTGRYTKAADVDLSGGRAAVEKHKFDPSLPGNARKLEAVGALSELASDAGLPLAHLAVAFVRAHPAITSVIIGPRTMEQLEDLLAGSEVELSEDVLDRIDEIVPPGTDLNPADSYYTPPALGDKRLRRR
>NZ_CP023992.1|WP_079258079.1|4529063_4529876_+|class-I-SAM-dependent-methyltransferase
MPARVPPPSRPIGSATRGTTNPNRLRRMDRWIAAAHGAALRRAGEPPVAVDLGYGAAPWTAVELLDRLRTVRGGTRVVGVEIDPGRVAAARPYEREGLTFAHGGFEVPLPGGARPALIRAANVLRQYEEGEVAAVWRRLCARLAPGGLLVEGTCDEIGRRHVWVALGPAGPRTVTFAARLGSLERPSDLAERLPKALIHRNVPGEPVHTFLRDFDRAWAAAAPYAPLSARQRWIRSAQTLRAAGWPLADGPRRWRQGEVTVRWEALAPRG
>NZ_CP023992.1|WP_099014150.1|4527560_4528922_-|D-inositol-3-phosphate-glycosyltransferase
MSQHASRLGGLRGRSHVPFGTPSHQRLRRMPRRPRRIAMLSVHTSPLHQPGTGDAGGMNVYIVELAKRLAAIDIEVEIFTRATTAALPPAVELAPGVLVRHVDAGPYEGLAKEDLPAQLCAFTHGVMQAWAGHRPGHYDLVHSHYWLSGHVGWLAAERWGVPLVHAMHTMAKVKNAALAEGDTPEPAARVIGEQQIVRAADRLIANTDEEAEELARHYEAARELVAVVHPGVNLDRFRPADGRAAARARLGLPADALIPLFAGRIQPLKAPDILLHAVAHLLEEDPSLRERIVVPVVGGPSGSGLAKPEGLHKLAARLGICDVVRFRPPCAQDELADWYRAASVLVMPSYSESFGLVAIEAQACGTPVVAASVGGLPVAVRDGVSGTLIHGHDPADYARALRPFAAEPERADRMGAAAARHAESFGWDTAAAATAEVYTEAMRERRRLRSGHG
>NZ_CP023992.1|WP_099014149.1|4527046_4527568_-|YbjN-domain-containing-protein
MADPMADTAPEADLRAVIERTLNDAELEWESPEDGTYVVTLPGTRKLSTTCSLRVGRHSLSVNAFVVRHPDENHAAVHRWLLERNTRLYGVSYAIDQLGDIYLVGKLPLAAVTPEELDRLLGTVLENADGSFNTLLEMGFATAIRKEYAWRTSRGESTRNLEAFSNLTRDAAK
>NZ_CP023992.1|WP_099014148.1|4525149_4526889_-|hypothetical-protein
MGMEIGRRRLLGGAMGLAAGATALGAGAPLLTATDAAAAPRTAGGTGGAGGTGDPGGARTSPLWQEFLDRPYTHPQLPYVGRAGYLGGRTSFPRPPVVADVRDYGARPDGSADAAPAINRAIEAAGRRGGGTVLVPPGTYRVDDVIRLGYDNVVLRGAGSGRTTLHATRNLTELIGPYGSRYGGDKSSWSWAGGLIWICPDARLRSLTDAIRARAWPFEGWTGNRRDEWRTLTGLAAPARRGDWTVTVEDPSALRPGDRVLLQLADDDTHSLLSHMAGDVEGAADYVWTDKTKLTSYVPYEWPCRVAAVDRGRGRVTLDRPLPLDARPAWRPRFTTLVPPVTGSGVEGITLDVVETPQAQHLLDKGYNGVALQCAWDCWVDDVTVNNVDNGFLLVAAKACTLRRTRVTGRGSHHPYCCREGSHDNLVEDFVLARRTVPAPAGTQLHGINVEGLSSYNVWSRGRMEMGTFDTHRGMPFANVRTEITVDNTGSHGGDASAGPLYGARFAHWNVTVTNERAGCVRIDDIAPYSATVGISEVRQFGQIDVPDFTGPLHSRIESYGHPEAVQPRNLYQAQRALR
>NZ_CP023992.1|WP_142881413.1|4524743_4524998_-|hypothetical-protein
MDNPWLTVATVVTVGVLRLMGDVIRWLAARSGERLRARTLAELVSRTEPGTVLTDRRPDGAALTIWRDTDRTVASGGAGRGRSA
>NZ_CP023992.1|WP_099014146.1|4521694_4523767_-|M48-family-metalloprotease
MIAAARAVLALALLAVFYALVAAMVLLWAAFLAAALWTAGAPGVQTPPMSVITACAAFAPIVFGMVWAVIRTARPAAAREDAVTVTRRGAPELWDTVEELALDIGTRPPGHIRLTAEANASVTEDAPLLGLAPGRRVLYLGLPLLAGLSRAELRAVLAHELGHFSRRHSRFGVVAHRGAAGLVAARQAIQDAAAANDLVRLYAGGPLLLLNLYTYVFRWLTRPVRRRQELEADREAARVAGPDAVADALRSTTALDAAWQEFLAEFLAPMRRATGRIPDDPFRAFAHMVEAPELREPLAALRARAVERPADPDDAHPALATRLERLARLPAAEPGTASLSLDPFSLDPLALRPRYAVALGRVMLPGPDAGTRVPWRDWLTELAEHRATRILPPLAEAAREVEETEGMGRKKANPEPKPEPGKEPGPESVTGSVTAPATEPDALTVQRVLWLLDSGRRMPLARALNSRLPHGERMFHGERTELDPLGPLAEALAVLIGAQLVAKGTAYWAMNWTGPSILVPPDGIAPETIRTWADTAVRLPGQTRQLGLHLAALGVDERAPLPSTDPAGDTADGPAPAGKARQISITPGITGPARRRIKAVGGLALTVLLLMTGLSLALWANSDDPSYPRVPVTRWTDRYQPGGGTGTEPAPFPTYQQPTFPARPTIPTFQLPPRSVPTIRIEPVIPRPAP
>NZ_CP023992.1|WP_099014145.1|4520041_4521592_+|MFS-transporter
MSVARLRQATKESVSGLPREFWWLWTSTLVNRLGGFVATFLAMYLTAGRGYSAMFAGLVGALYGLGGAVSAVVAGVLTDRLGRRPTLLVSQLSTAATVAALGFVQDPVAIAVVACLVGMTSNASRPAVQAMIADIVAPKDRVRAFSLNYWAINLGFAVSAAAAGLIARHGYLTLFLADAGMTLACALIVFGKLPESRPARPEPGGAALGADAPEPAVGLGTVLRDRRFMAVVGLSFLIATLIQQAFVALPVAMGADGLSSTDFGLAIATNGALIVAVQIPVTRFLERREPAPLLIVSALLTGAGFGLTAFAGSVGMYAVAVTVWTLGEIINSPTQMGLVARLSPTHGRGRYQGMYTLSWSLASLIAPLAGGAVMDRFGADALWASSAVVGLVAAGGYAALGRAMRSRPTAGGSGGSEGSGASGASGASGASGASGASGASGASGASGASGGGVGGAAGGSAPVVGAGVGDEAGGASDGAAHAGGVGAGGEVRSSSGGSAPAVGAAPGLAVGDASDG
>NZ_CP023992.1|WP_069860843.1|4519136_4519898_-|phosphoglyceromutase
MADAPYKLILLRHGESEWNAKNLFTGWVDVNLNEKGEKEAVRGGELLKDAGLLPDVLHTSLLKRAIRTSQLALDAADRLWIPVRRSWRLNERHYGALQGKDKAQTLAEFGEEQFMLWRRSYDTPPPPLEDGAEWSQSDDPRYATIPPELRPRTECLKDVVERMLPYWYDGIVPDLLAGHTVLVAAHGNSLRALVKHLDGISDADIAGLNIPTGIPLSYDLDTDFRPVTPGGTYLDPDAAKAAIEAVKNQGKKK
>NZ_CP023992.1|WP_093699731.1|4536501_4537311_+|deaminated-glutathione-amidase
MRIAVGQFAATPDWKDNLAACQELTAQAVRGGADLLVLPEGVLARFTEDRHRIREVAQPLDGPFVSEMLAATAGSATTVVVGIHEPSEDGRVFNTLVALRDGELIARYRKIHLYDAFGDLESANVRPADEPPVVIDVAGTKVGLMTCYDVRFPELARLLVDAGAEVLALPAAWVRGPAKERHWEVMITARALENTCWVAASGECGPRNIGNSLVVDPLGTVRSRLAAAPGLAWADAAPDTTAAARRTLPVLANRRFAVDPTVIPLGAPQ
>NZ_CP023992.1|WP_099014152.1|4537319_4538255_+|ABC-transporter-substrate-binding-protein
MRRPLATATTALSCCLALAACGANPPQAEGAGGSSGGDAKASAKLPEDKALHALLPTKNRTSGTLVSVNNGSFPPYEIAGSDGHSLTGASADLADSLGQVLGVKIRHVTTDGLPSQLTGIKAGRYDFALGPVGDFKDRQGANDFVDWVREFVVFAVPKGNPHHISSLADTCGQRIAVMAGGSAEGVIKKQALTCEKDGKKPVKVQSYKDQPGSILAVRSGRADAFFSSQAPLTYFVAQAKDQLELTGTGKGNGFDDLYQGAVVAKGSPLRDVLLKALRKLIDDGTYGKIMKKWGLSANTLDKPGVNLGGES
>NZ_CP023992.1|WP_099014153.1|4538279_4539299_+|amino-acid-ABC-transporter-permease
MATTQPPATRDDPGAAELPPGAVPDVDVAGASPVRHPLRWLAVLLLAVLCAQLIHFLITNPHFEWGTVGAYFGAQVIGQGIATTVELTAIAMLIGVAGGVLVAVGRMSENRVLSTVCGAYVWFFRGIPVLVQLVFWYNLSALLPRISFGVPFGPEFISGQTNTLITPWLAAILGLGLNEAAYMAEIVRGGLLGVDQGQTEAAAALGMGRARILRRVVLPQAMRFIIPPTGSQVINMLKATSLVSVLALADLLYTVQSIYNRTFETIPLLIVACLWYLVMTSVLYVGQSFIERYYARGATRHAPQGFWAFALFRRRPDTPSPAADSPSPAADRPLAKEET
>NZ_CP023992.1|WP_079152843.1|4539355_4540108_+|amino-acid-ABC-transporter-ATP-binding-protein
MVVAQRVRKRFGQLEVLRGIDLEVRRGEVVVLLGPSGSGKSTFLRCINHLEQIDAGSIHVEGRLIGFRKSGGRVHHLRPREVTRQRRDIGMVFQHFNLFPHQTVLENVIEAPVGVLGLPKAEARKTATELLTRVGLADKAASYPRQLSGGQQQRVAIARALAMRPKLMLFDEPTSALDPELVGEVLATMRDLARDGLTMLVVTHEIGFAKEVADRVVFMDDGQVLESGTPREVLDSPTNPRTRAFLSRFL
>NZ_CP023992.1|WP_099014154.1|4540177_4540627_-|NUDIX-hydrolase
MNRRNSHGDGGADTGTVLAAGCVLWRRSPHGGRLEIALVHRPRYDDWSHPKGKLKQGEDALRGAVREVAEETGMGCAPGAVLPTLHYVARGRPKEVRYWAAEAVDDETFVPNREVDRLVWLPPDIARNRLTYDHDRTLIDALLHALRPS
>NZ_CP023992.1|WP_099016987.1|4540734_4542369_-|CHAD-domain-containing-protein
MTGAADPAADPARPGNDGVTDRAAEAVAAPSWESVTAGEVLSAYLHAQAGDFLRSLRLHRESGSDVQEAAEAARLLRRSARRISGALYVYRPLTDTAWSDELRTELAWLSGTLAREHAYEERLERLRGALHRLSGAGGPSDRSPQGEAEATTPGERLPDGAVGAAHTASANAAHATAASAARTARGGVTVAVDGAGGPSGAPGSVPRSPRAARRSVSLAAGAPGGGAADPVGGQGARPGPADTGGGAEGAAGTSRDRDEGRTAGRRRGERGDKGGRGTKGEKGERTGQPGAAHQRAGAEEEARGGALTVGAARAGALLERQLTLARTRAHTAALEALGSSRFHAVADTVALLASEAPLDDAGAARPAGQVLPPLADLANRRLTEAVEALPLIRAGHPYNAEALVHGLAATSAADAPPASERQDAPWHQVRHLLRLRRYALEVLDRAAWQQDGPSGANGTGPTGPGAADAEPPLSVRLLAAGQALERHRDAAEAAAAAAAAARTPRIAPATAYALGVLHADQRHEVEAARFAFGRIWRRVAARAS
>NZ_CP023992.1|WP_069860855.1|4542385_4544641_-|RNA-degradosome-polyphosphate-kinase
MSHTSGPASVSPQPQPQHQPSVGSIAAHRPHAVAMRPVRSLDPDLDADLDSYEEGAGPDADGGELPQGRFLDRERSWLAFNERVLELAEDPATPLLERANFLAIFASNLDEFFMVRVAGLKRRIATGVATRSASGLQPREVLELIWNRSRELMARHAACYQQDVAPALAEEGIHLVRWPDLTEKEQSRLFTLFRQQIFPVLTPLAVDPAHPFPYISGLSLNLAVVVRNPVSGHDHFARVKVPPSLSRFLEASPQRYVPLEDVIAAHLEALFPGMEVLAHHMFRVTRNEDLEVEEDDAENLLQALEKELLRRRFGPPVRLEVEESIDPYVLDLLVRELKISDAEVYPLPGPLDLTGLFGIAALDRPELKYPKFVAGTHRDLAEVESASPPDIFAALRERDVLLHHPYDSFSTSVQAFLEQAAADPDVLAIKQTLYRTSGKSPIVDALIDAAESGKQVLVLVEIKARFDEHANIKWARKLEEAGCHVVYGLLGLKTHCKLSLVVRQEGDTLTRYSHVGTGNYHPKTARLYEDLGLLTANSQVGADLSDLFNRLSGYSRRENYRRLLVAPKSLRGGLITRINKEITHHRSGRPAYIKIKVNSMVDEAVVDALYRASQAGVPVDVWVRGICALRPGVPGLSENIRVRSVLGRFLEHSRVFAFGNGGEPEVWIGSADMMHRNLDRRIEALVRVTDPGHRAALNRLLDTGMSDSTSSWHLGPDGEWTRHATDADGQPLRNVQEMLIDARRRRRGSTT
>NZ_CP023992.1|WP_099014155.1|4545027_4545960_-|mycothiol-synthase
MNDVVNETSGARRLDVLEELSSAEARDVLRLIAEAARIDGQQAVSEQGRLQLRGRREGVRHLVLREPSGELAGYAQLEDTDPVEAPAAELVVHPARRGQGHGRALGVTLLKESGKRLRVWAHGGHASARHLAQVLGLTLFRELRQMRRPLGSLAELGLPEPALPEGVTVRTFRPGEDDTAWLAANAAAFAHHPEQGSLTQRDLDDRKGEPWFDPEGFFLAERDGEIVGFHWTKVHAEERLGEVYVVGVRPDAQGGGLGKALTSVGLRHLAARGLPTAMLYVDADNFAAVAVYERLGFVTHETDLMYRTET
>NZ_CP023992.1|WP_099016988.1|4546022_4547090_-|DUF1016-domain-containing-protein
MQNELTKRTPIPAQGSELPPGFFELVDDLKAIVTQASTRAQLKVNTEMIKMYWEIGRTILDRTEREKWGSKVLERVATELRTAFPNQRGFSRSNLKYMQQMARLWPEPIGQQAVGQLPWGHITLLMGRCKTRPELDFYAQRAVQQGWSRVMLDHWIDAQLHLTQGAALNNFDATVPEDSDAVNEVVRDPYRVDFTRLSGKVAERDLEDALVQQLVRFLTELGVGFAFVGRQYPIKVGDEEFRIDLLFYHCKLHRYVVIELKTDKARPAHLGQLGFYVTVVDDLVRDKERDDPTLGILIARSRDKGTIEYALRSNNAPLAVSTYAALPPHVRELMPSAEDLSRIADDILDGDGAAG
>NZ_CP023992.1|WP_099014156.1|4547277_4549098_+|bifunctional-metallophosphatase/5'-nucleotidase
MPARPQRRGAGRRLATGFAVLAAAAGVLTAVSPAGADSAAASDKHRPGSTVDVQLLSFNDLHGNLEPPQGSSGTVAETQPDGTTKTIPAGGAEYLATSLRNARKGHDYSITAAGGDMIGASPLLSGLFHDEPTIEALNKLDLDVTAVGNHEFDEGRTELNRIQNGGCHPKEGCYEKGKTFEGADFPYLAANVTDEKTGKPILKPYTVWQHKGVKIGFIGVTLEGTPDIVTAEGVKGLKFHDEVETINKYAKELQGKGVKSIVALIHEGGLPASSSYNYDCDNGGAGKGISGPIVDIAKNITPTVDALVTGHTHQAYTCTIPDPSGTPRTVTSAASFGRLYTDTTLTYDRRTGDIVRTSVKGANAANHVVDRDQPKAPDMTSLIGRWNKLAAPVAGKPVGYISADVNGRGSSAYETPLGDVIADGQLEALAPADKGGAQLAFMNPGGIRSDLAYTASGSEGDGVVTYGEAFTVQPFTNMMNVIDLTGSHLITALQQQVSGSNEASPRILQVSKSLTYTLDLTKSGKDRIVTDSVKLNGEPIDPAKTYRVALNEFIAGGGDGFPVFKEGKNKLVGASDLDTFTAYLGAHSSQSAPLDPPKADRITIVK

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Crispr_ID: NZ_CP023992_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_12

5325498-5325638

Orphan

Consensus_repeat	Method
GCCGTCGCTCGGCGGGGGCCCGCCG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP023992_12

>merge|NZ_CP023992|12|5325498-5325638|CRISPRCasFinder
GCCGATCCTGGGCGTGGTCCGGCCGGACGCGAGGTAGTGCGGCGGGAGTTTGCCGTCGGTCGGCGGTGGGCTGCCGTCGCTCGGCGGGGGCCCGCCGTCGAAGGGCCTGCCCGGGCCGCCGGGTTCGGCGGGGGTCCGCCG

>NZ_CP023992|12|12|5325498-5325638|CRISPRCasFinder
GCCGATCCTGGGCGTGGTCCGGCCG	GACGCGAGGTAGTGCGGCGGGAGTTT
GCCGTCGGTCGGCGGTGGGCTGCCG	TCGCTCGGCGGGGGCCCGCCGTCGAAGGGCCTGCCCGGGC
CGCCGGGTTCGGCGGGGGTCCGCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_093700724.1\|5334139_5334895_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367243
NZ_CP023992.1\|WP_069873632.1\|5318463_5319462_+\|inorganic-phosphate-transporter	unknown	unknown	gnl\|CDD\|376541
NZ_CP023992.1\|WP_079258466.1\|5320476_5321547_-\|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl\|CDD\|223654
NZ_CP023992.1\|WP_099014474.1\|5322862_5323990_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	unknown	unknown	gnl\|CDD\|273374
NZ_CP023992.1\|WP_162502103.1\|5316714_5317140_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|173412
NZ_CP023992.1\|WP_069873630.1\|5319673_5320450_-\|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|184587
NZ_CP023992.1\|WP_069873618.1\|5326613_5327840_+\|fused-response-regulator/phosphatase	unknown	unknown	gnl\|CDD\|369272
NZ_CP023992.1\|WP_099017030.1\|5330219_5331410_+\|RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|227277
NZ_CP023992.1\|WP_093703234.1\|5329698_5330055_+\|transcriptional-regulator	unknown	unknown	gnl\|CDD\|226318
NZ_CP023992.1\|WP_099014471.1\|5315600_5316515_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069873634.1\|5317237_5317642_-\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376835
NZ_CP023992.1\|WP_079258473.1\|5332473_5333007_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379112
NZ_CP023992.1\|WP_099014473.1\|5321757_5322747_-\|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl\|CDD\|223646
NZ_CP023992.1\|WP_079258470.1\|5325852_5326377_-\|O-acetyl-ADP-ribose-deacetylase	unknown	unknown	gnl\|CDD\|234759
NZ_CP023992.1\|WP_099014469.1\|5313539_5315156_-\|FAD-binding-oxidoreductase	unknown	unknown	gnl\|CDD\|223354
NZ_CP023992.1\|WP_030837909.1\|5317834_5318455_+\|DUF47-domain-containing-protein	unknown	unknown	gnl\|CDD\|224310
NZ_CP023992.1\|WP_069873614.1\|5329069_5329483_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP023992.1\|WP_167460028.1\|5331525_5332371_+\|oxidoreductase	unknown	unknown	gnl\|CDD\|236676
NZ_CP023992.1\|WP_069873670.1\|5327899_5328217_-\|DUF2516-family-protein	unknown	unknown	gnl\|CDD\|378483
NZ_CP023992.1\|WP_099014476.1\|5328364_5329051_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_093700724.1\|5334139_5334895_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|367243	pfam02909, TetR_C, Tetracyclin repressor, C-terminal all-alpha domain.	1.7032e-16
NZ_CP023992.1\|WP_069873632.1\|5318463_5319462_+\|inorganic-phosphate-transporter	gnl\|CDD\|376541	pfam01384, PHO4, Phosphate transporter family. This family includes PHO-4 from Neurospora crassa which is a is a Na(+)-phosphate symporter. This family also contains the leukaemia virus receptor.	3.87665e-100
NZ_CP023992.1\|WP_079258466.1\|5320476_5321547_-\|phosphate-ABC-transporter-permease-PstA	gnl\|CDD\|223654	COG0581, PstA, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	5.2336e-85
NZ_CP023992.1\|WP_069873618.1\|5326613_5327840_+\|fused-response-regulator/phosphatase	gnl\|CDD\|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	9.28051e-37
NZ_CP023992.1\|WP_099014474.1\|5322862_5323990_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	gnl\|CDD\|273374	TIGR00975, precursor_PBP-3_PstS-3_Antigen_Ag88., phosphate ABC transporter, phosphate-binding protein. This family represents one type of (periplasmic, in Gram-negative bacteria) phosphate-binding protein found in phosphate ABC (ATP-binding cassette) transporters. This protein is accompanied, generally in the same operon, by an ATP binding protein and (usually) two permease proteins. [Transport and binding proteins, Anions].	1.35516e-78
NZ_CP023992.1\|WP_162502103.1\|5316714_5317140_+\|hypothetical-protein	gnl\|CDD\|173412	PTZ00121, PTZ00121, MAEBL; Provisional.	4.25375e-09
NZ_CP023992.1\|WP_069873630.1\|5319673_5320450_-\|phosphate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|184587	PRK14241, PRK14241, phosphate transporter ATP-binding protein; Provisional.	0
NZ_CP023992.1\|WP_093703234.1\|5329698_5330055_+\|transcriptional-regulator	gnl\|CDD\|226318	COG3795, COG3795, Uncharacterized protein conserved in bacteria [Function unknown].	7.8605e-23
NZ_CP023992.1\|WP_099017030.1\|5330219_5331410_+\|RNA-polymerase-sigma-factor	gnl\|CDD\|227277	COG4941, COG4941, Predicted RNA polymerase sigma factor containing a TPR repeat domain [Transcription].	1.26618e-151
NZ_CP023992.1\|WP_069873634.1\|5317237_5317642_-\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|376835	pfam02583, Trns_repr_metal, Metal-sensitive transcriptional repressor. This is a family of metal-sensitive repressors, involved in resistance to metal ions. Members of this family bind copper, nickel or cobalt ions via conserved cysteine and histidine residues. In the absence of metal ions, these proteins bind to promoter regions and repress transcription. When bound to metal ions they are unable to bind DNA, leading to transcriptional derepression.	5.51229e-31
NZ_CP023992.1\|WP_079258473.1\|5332473_5333007_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	9.4646e-11
NZ_CP023992.1\|WP_099014473.1\|5321757_5322747_-\|phosphate-ABC-transporter-permease-subunit-PstC	gnl\|CDD\|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	6.36773e-86
NZ_CP023992.1\|WP_079258470.1\|5325852_5326377_-\|O-acetyl-ADP-ribose-deacetylase	gnl\|CDD\|234759	PRK00431, PRK00431, ADP-ribose-binding protein.	4.92961e-87
NZ_CP023992.1\|WP_099014469.1\|5313539_5315156_-\|FAD-binding-oxidoreductase	gnl\|CDD\|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	7.85266e-30
NZ_CP023992.1\|WP_030837909.1\|5317834_5318455_+\|DUF47-domain-containing-protein	gnl\|CDD\|224310	COG1392, COG1392, Phosphate transport regulator (distant homolog of PhoU) [Inorganic ion transport and metabolism].	8.83285e-31
NZ_CP023992.1\|WP_069873614.1\|5329069_5329483_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	1.37847e-14
NZ_CP023992.1\|WP_167460028.1\|5331525_5332371_+\|oxidoreductase	gnl\|CDD\|236676	PRK10376, PRK10376, putative oxidoreductase; Provisional.	2.22684e-90
NZ_CP023992.1\|WP_069873670.1\|5327899_5328217_-\|DUF2516-family-protein	gnl\|CDD\|378483	pfam10724, DUF2516, Protein of unknown function (DUF2516). This family is conserved in Actinobacteria. The function is not known.	3.34374e-31

>NZ_CP023992.1|WP_099014474.1|5322862_5323990_-|phosphate-ABC-transporter-substrate-binding-protein-PstS
MKLQRKNRLRAIVAGALAVSGALVLTACGSDDNSGDAKDGGGSKAASNIKCDGKGQLLASGSSAQKNAMDLWIKTYGAACKDTKLNYKATGSGAGIQEFLQGKTAFAGSDSALKPEEVKSSEKVCKGGKAIDLPMVGGPIAVGFNVPGVDKLTLNAETLAKIFDSEITKWDDPAIKALNKDAKLPSLKIQAFHRSDESGTTDNFTKYLKAASPKAWPHEPGKAWEGKGGQSADGSSGVSSQVKQVSGAISYFELSYATANSIKTVDLDTGASAPVQATVDNASTAISEAKIKGTGSDLALDLAYDTKAANAYPITLVTYEIACDKGNKADTLAATKSFLTYVASEDGQTSLKELGYAPLPTEIANKVRESVKSLS
>NZ_CP023992.1|WP_099014473.1|5321757_5322747_-|phosphate-ABC-transporter-permease-subunit-PstC
MKTDIEPTSSVAGSPSKVKTRSTGRAGDKIFLGLSRGSGIALLVIMAAIAAFLTYRAAIAISKDEANFLTTFEWNTSTSPMRFGIAVLAYGTVVSSIIAMVIAVPVAVGIALFISHYAPRRLATPVAYVIDLLAAVPSIVYGLWGALFLVPHLTGLYTWFDDYLGWTGIFSYQGGAARSLFTVGILLAIMILPIVTSVSREVFRQVPKMHEEAALALGATRWEVIRMSVLPFGRSGIISASMLGLGRALGETMAVATVLSPNFLIETSLLDPGGGTFAQNIASRFKEAGDDGRDALIASGLVLFVITLLVNGAARMIIARRKEYSGTAA
>NZ_CP023992.1|WP_079258466.1|5320476_5321547_-|phosphate-ABC-transporter-permease-PstA
MSSNAVVDKGGSRHGSSLQQARLPQWAPYALVVVSLALGAGIGTALGMDSPFQWGLFAALVFIVASYVLGAVVEGGRQARDRLATSLVWVCFLLAVVPLLSLIWETVDRGRTVLDGYFLGHSMEGVQTILPGGGAYHAIIGTLEQVGLAALIAVPIGLLTAIYLVEYGRGKLAKAVTFFVDVMTGIPSIVAGLFILSFWIIILGFSYSGFAGAMALAILMMPIVVRSTEEMLKLVPDELREASLALGVPKWRTILKVVLPTAIGGITTGVMLAVARVAGESAPIVLLVFGATGINNNPFEGAQSSLPYYIYEQWQLGNEASFNRAWAAALVLIAFVMILNLVARGIARWKAPKSGR
>NZ_CP023992.1|WP_069873630.1|5319673_5320450_-|phosphate-ABC-transporter-ATP-binding-protein
MAKRIDVSGLTAYYGSHKAIEDISMTVEPRSVTAFIGPSGCGKSTFLRTLNRMHEVTPGGRVEGKVMLDDENLYGSGVDPVSVRRTVGMVFQRPNPFPTMSIFENVAAGLKLNGSYKKSELENVVEKSLKGANLWNEVKDRLNKPGAGLSGGQQQRLCIARAIAVEPAVLLMDEPCSALDPISTLAIEDLIGELKERFTIVIVTHNMQQAARVSDRTAFFNLAGVGQPGKLIEIDETERIFSNPSVQATEDYISGRFG
>NZ_CP023992.1|WP_069873632.1|5318463_5319462_+|inorganic-phosphate-transporter
MDTFALVVTIAVALFFTYTNGFHDSANAIATSVSTRALTPRAALAMAAVMNLAGAFLGSGVAKTVSEGLIATPTGDQGMMILFAGLVGAITWNMVTWYFGLPSSSSHALFGGLVGAALAGASTVHWDGVLEKVVIPMVISPIVGLILGYFVMVIILWLFRDANPHKAKRGFRIAQTVSAAGMALGHGLQDAQKTMGVVVMALVIGGVEDEGDAIPVWVKISCAAMLSLGTYAGGWRIMRTLGRRIIELDPPQGFAAETTAAGVMYTASFMFQAPISTTHVITSAIMGVGATKRVSAVRWGVAKNIVLGWFITMPAAAGVAALSYWIVNLAFG
>NZ_CP023992.1|WP_030837909.1|5317834_5318455_+|DUF47-domain-containing-protein
MRFRLTPRETSFYDMFAASADNIVTGSKLLMELLGADSSARAEIAERMRAAEHAGDDATHAIFHQLNSSFITPFDREDIYSLASSLDDIMDFMEEAVDLVVLYQVEELPKGVEQQIEVLARAAELTAEAMPNLRTMTNLTEYWIEVNRLENQADQIHRKLLAHLFNGKYDAIEVLKLKQIVDVLEEAADAFEHVANTVETIAVKES
>NZ_CP023992.1|WP_069873634.1|5317237_5317642_-|metal-sensitive-transcriptional-regulator
MTTTAADTTAPNDGDERGQASGHTSAQESVPHGGHGYAKQKDQHLKRLRRIEGQIRGLQRMVEEDVYCIDILTQVSAGTKALQSFALQLLEEHLRHCVASAAVESAARGEEEGTSEVDTKVAEATAAIARLLRT
>NZ_CP023992.1|WP_162502103.1|5316714_5317140_+|hypothetical-protein
MIAASSADEDRLSTDRIDEVLRVRADRSDSAEGAKGARGAKGVRRPKGAGGAGGAGGAGGAEGTKGAQGAQRAEDAKRAQEMKSAPDANRAQDTHRAQDMKDAPEANHVTEAHRAQDAKAAEDAKGAPEALAPEAGGPDAP
>NZ_CP023992.1|WP_099014471.1|5315600_5316515_+|hypothetical-protein
MEFQQRGLGVRRRVRAAAGLVSGGLLAVSLATVSGCSTETAADERPAGAARESAVAALHRAADVLVKSGSSRVRTTMETATGGTRVSIRGTGAYDFEKRLGRLRLLLPKDAMGTAEHAPITELLAPGALFMRNRGAGIPRDKWVRVDTTDIPDGNLVTGGATDPLIAAELLRGARKASLVGEEGLGGDLVRHYRGTTDIGRAARVASEGVRGSLMAAARGFGESTVPFDAYLDGLGRLREVRHRFTMAGRADGQEATEGAGAAGRPDALGVASTTQLYDFGAPALIELPKPTDIYTGKVGSPQK
>NZ_CP023992.1|WP_099014469.1|5313539_5315156_-|FAD-binding-oxidoreductase
MNRRTLLAAGTGLAATATWVTACDDGTGKAGGDSSSGGSASSSASDARSASASGRRGAVDGKPKSADWSALGKDLQGDLVRPGDSDYTSASRLYNTRFDHLRPAAVAYIANTSDISACLDFARRHGAPVAIRNGGHSYAGWSSGDGRLVIDVSALSSIRTSSGEARIGAGAKLIDVYTSLGARGVTVPGGSCPSVGISGLTLGGGHGVVSRAYGLTADSLTGATIVTADGKALEVSKNREAELFWALRGAGNGNFGVVTELRFRTHEAADGVTCYMSWPWSKAAKVLSAWQKWGPDQPDEIWSALHLSAAPGGTPTVSVSCFSLGTYGALQNAVDRLADGPGGPGPASQVSLRRRGYVDAMRMYAGCGDTSTANCHLPGDKPGRNTSGVLNRETYAARSDFYDRSLSQAGVRAMLDQVERYGRRTGGGGAVSIALTALGGAVNRVSPTATSFVHRRSRFLAQYTASWAASGSGTAGNAWLDGAHTAMRRYASGAAYQNYTDASLKDWRTAYYGSAADKLSRVKKRYDPDRLFDFPQAL
>NZ_CP023992.1|WP_079258470.1|5325852_5326377_-|O-acetyl-ADP-ribose-deacetylase
MTNITLTLGDITEQRVDAIVNAANSSLLGGGGVDGAIHRRGGPDILDECRDLRASRYGKGLPAGRAVATTAGRLPARWVIHTVGPVFSTTEDRSATLASCYSESLRIADELGARTVALPAVSTGVYRWPLDSAARIALTTVRDMGTSVTEARFVLFDQRAYDAFETALNELPPA
>NZ_CP023992.1|WP_069873618.1|5326613_5327840_+|fused-response-regulator/phosphatase
MSVPVPRQREAPAPSAGPATLPENGLTLLVIEDDPSGAFNVPEMLDTEGNRVRIRTARNLTEASRLLTDGVQCILLALPGPSEDGPDSLATLRRVLKLAPSHAVLVLTAEDDAERAAEAVRVGAQDFLFRGELDGRVLSRAIRYAVERKRSDLAQRQLTESRLRAQENARLERGLLPTPLLDGSGLHFAARYRPGRSRALLGGDFYDTVRTPDGTVHAMIGDVCGHGPDEAALGVELRIAWRALTFAGLCGDQLLGTLQQVLENERADDEIFATLCTVDIAPDGRRAGVCLAGHPSPLAIRPSMAPRLLPTDENGPALGLLPNARWPRREVELGGAWSLMMYTDGLIEGRVGSGVQRLGQDGMVEIVARQVAEGRRGEELLDATVTEVRALNGGELTDDLAVLLLDRD
>NZ_CP023992.1|WP_069873670.1|5327899_5328217_-|DUF2516-family-protein
MYWVSWALLLFSLFAFVDSAIRREDAYRAADKQSKAFWLIILGLAAAVNFFMGILDFLPIIGLIATIVYIVDVRPALRQVSGGGRRWPRGRGSSSDGPYGPFNGR
>NZ_CP023992.1|WP_099014476.1|5328364_5329051_-|hypothetical-protein
MAITDDVRKTLTDPTPLYFVAGTADLAAQKLKEVPSFVEKIVAEAPERINAVRNTDPKAVQERVSQQAKGAQDKLSEMLGTIDTDIKRLRDTAQDLALQGVGRAAELAVKARERYDEVAEHGQEVVRTWRGEAADEVVDIADAIEPKQERDGHTAARSKAPSQSVHMDSSKESPKSPAKPATPAASSGSGPSAAHTPAHSSSAQAKKAPARGNKPATAAKKPEPKSAG
>NZ_CP023992.1|WP_069873614.1|5329069_5329483_-|helix-turn-helix-transcriptional-regulator
MASLNVGNLGEFLREQRRSAQLSLRQLADAAGVSNPYLSQIERGLRKPSAEILQQLAKALRISAETLYVQAGILDERDREETEVRSVILADPSINERQKQVLLQIYESFRKENGLQTASDDAPEPSDAGADVATPSN
>NZ_CP023992.1|WP_093703234.1|5329698_5330055_+|transcriptional-regulator
MPRYLTMIRIDEQNAPAEGPSPELMERMGALIEEATKSGVMLETAGLTPTSAGTRVTWSGGKITCTDGPFTESKEVIGGYAILQAKDKAEAVEWTKRFLRTHEEYWTITIEVREIEEG
>NZ_CP023992.1|WP_099017030.1|5330219_5331410_+|RNA-polymerase-sigma-factor
MESARIIAGVARIVRDVGLAEELAQDALVTALERWPESGVPDNPGAWLMATAKHRAIDLVRRKETYARKLTEVGRDLEDVSPPDPADLAGTAEDIDDDLLRLIFTACHPMLSTRARVALTLRLLGGLTTEEIARAFLVPEPTVAQRIVRAKRTLAKAEVPFEVPYGDDRTARLSSVLEVIYLIFNEGYSATTGDDLVRPALCEDALRLARVLAGLLPQEPEVHGLAALLEFQSSRIAARTGPDGAPVLLADQNRTRWSGLLIRRGVDALQRAGHGPYSLQAAIAACHARAIRYEDTDWTAIAALYGRLMALAPSPVVELNRAVAVAMAEGPAAGLKLVEALAEEPALKDYHLLPSVRGDLLERLGRYVEARVEFARAAALTRNARERALLLERSSG
>NZ_CP023992.1|WP_167460028.1|5331525_5332371_+|oxidoreductase
MLAQLSSPADRLGFGAMQLPGRWAGPVVERATAVAVARRAVELGARHIDTAAFYFSATARANDILREALRPYPEGVTIATKIGPLRTATGEMYAEARPEQLRGLVEENLRQLGVDALDLVYLRVGRLKAVGGASIGERFAALAALREEGLVRRLGVSNVSADQLAEARAIAPVAAVQNRFGVLDQADGPLVDECAGAGIAYVPFFALGGGHTSLEGENLRTVAERHGATAHQIALAWGLARSPAIIQIPGTSSLAHLEENMAAARIALDEDDMALLEPVAD
>NZ_CP023992.1|WP_079258473.1|5332473_5333007_+|GNAT-family-N-acetyltransferase
MSGAASGVRVRLEPWEDSAFCLELLRRVNSAEMTAHLGGPESEEQILVRHRRYAELTGPGAGRMYRVVLVPEEETVGSIGYWEREWRGASVYETGWAVLPPFQGRGIAAAAAGEVARAAAAQRTHRYLHAYPSVGHPASNGVCRKAGFTLVGECEVEYPLGTMMRCNDWRLELWPPA
>NZ_CP023992.1|WP_093700724.1|5334139_5334895_-|TetR/AcrR-family-transcriptional-regulator
MASEVSGTGLPASIETAWGLRERPSKGPRPGLTLARIVDAAVGIASTDGLGAVSMSRVATELGASTMSLYRYVSAKDELLTLMEDAAYGPPPPGDPAKDADWRAGFGDWAWALRTALARHPWVVSVPIDTPPSMPNSVAWMERGLACLRHTNLGEGEKISVLMLVSGFVRNEVRMTFDILAANRRTGDSIETSLASWARLLGKVTDAERFPAVTAALRAGELETPGGPDDEFVFGLERILDGVEALISARS

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Crispr_ID: NZ_CP023992_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_13

5997736-5997950

Orphan

Consensus_repeat	Method
TCGACCGGCGGCTCGGCAGGCGG	CRISPRCasFinder

4 spacers

The CRISPR arrays of NZ_CP023992_13

>merge|NZ_CP023992|13|5997736-5997950|CRISPRCasFinder
GCGGCTGGGGGGTCGGCAGGCGCTGTGGCCAGCCGCTCGTGGGGTGGTTCGTCCGGTGGTGCTTCCGGCGGCCCCTCTGCCGACTTGTCCGGTGCTGGGTCTGACGGCTCGACCGGCGGCTCGGCAGGCGGTTCGCCCGGCGGTTCGCCCGGCGGTTCGCCCGGCGGCTCGGCAGGCGGCCCGCCCGGCGCCTGGTCCGGGGCCTCGTCCGGCGC

>NZ_CP023992|13|13|5997736-5997950|CRISPRCasFinder
GCGGCTGGGGGGTCGGCAGGCGC	TGTGGCCAGCCGCTCGTGGGGTGGT
TCGTCCGGTGGTGCTTCCGGCGG	CCCCTCTGCCGACTTGTCCGGTGCT
GGGTCTGACGGCTCGACCGGCGG	CTCGGCAGGCGGTTCGCCCGGCGGT
TCGCCCGGCGGTTCGCCCGGCGG	CTCGGCAGGCGGCCCGCCCGGCGCC
TGGTCCGGGGCCTCGTCCGGCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_099014742.1\|5988185_5988896_-\|hemolysin-III-family-protein	unknown	unknown	gnl\|CDD\|224191
NZ_CP023992.1\|WP_099014745.1\|5999251_6001264_+\|CocE/NonD-family-hydrolase	unknown	unknown	gnl\|CDD\|225487
NZ_CP023992.1\|WP_079153059.1\|5995825_5996680_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP023992.1\|WP_099014741.1\|5985200_5987237_+\|thioredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|224250
NZ_CP023992.1\|WP_099014749.1\|6007936_6009172_+\|sugar-kinase	unknown	unknown	gnl\|CDD\|238571
NZ_CP023992.1\|WP_099014740.1\|5981789_5985077_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP023992.1\|WP_069864602.1\|5993190_5994804_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173868
NZ_CP023992.1\|WP_079258784.1\|6009998_6010412_+\|RidA-family-protein	unknown	unknown	gnl\|CDD\|100004
NZ_CP023992.1\|WP_099014748.1\|6006500_6007790_-\|amino-acid-deaminase	unknown	unknown	gnl\|CDD\|143492
NZ_CP023992.1\|WP_069864583.1\|6010671_6012144_+\|permease	unknown	unknown	gnl\|CDD\|308194
NZ_CP023992.1\|WP_107429818.1\|6003193_6003850_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|375435
NZ_CP023992.1\|WP_069865530.1\|5991700_5992912_-\|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl\|CDD\|181738
NZ_CP023992.1\|WP_099014746.1\|6002111_6003095_-\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176203
NZ_CP023992.1\|WP_099014743.1\|5991158_5991569_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069864592.1\|6001230_6001908_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|184958
NZ_CP023992.1\|WP_069864585.1\|6009168_6010002_+\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP023992.1\|WP_099017065.1\|5989142_5990996_+\|phosphoenolpyruvate-carboxykinase-(GTP)	unknown	unknown	gnl\|CDD\|235256
NZ_CP023992.1\|WP_069864600.1\|5994809_5995769_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223674
NZ_CP023992.1\|WP_099017064.1\|5981462_5981711_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014747.1\|6004005_6005622_-\|D-aminoacylase	unknown	unknown	gnl\|CDD\|238622

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_099014742.1\|5988185_5988896_-\|hemolysin-III-family-protein	gnl\|CDD\|224191	COG1272, COG1272, Predicted membrane protein, hemolysin III homolog [General function prediction only].	8.71667e-49
NZ_CP023992.1\|WP_099014745.1\|5999251_6001264_+\|CocE/NonD-family-hydrolase	gnl\|CDD\|225487	COG2936, COG2936, Predicted acyl esterases [General function prediction only].	1.46915e-119
NZ_CP023992.1\|WP_079153059.1\|5995825_5996680_+\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.55725e-79
NZ_CP023992.1\|WP_099014741.1\|5985200_5987237_+\|thioredoxin-domain-containing-protein	gnl\|CDD\|224250	COG1331, COG1331, Highly conserved protein containing a thioredoxin domain [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP023992.1\|WP_099014749.1\|6007936_6009172_+\|sugar-kinase	gnl\|CDD\|238571	cd01166, KdgK, 2-keto-3-deoxygluconate kinase (KdgK) phosphorylates 2-keto-3-deoxygluconate (KDG) to form 2-keto-3-deoxy-6-phosphogluconate (KDGP). KDG is the common intermediate product, that allows organisms to channel D-glucuronate and/or D-galacturinate into the glycolysis and therefore use polymers, like pectin and xylan as carbon sources.	3.45476e-82
NZ_CP023992.1\|WP_099014740.1\|5981789_5985077_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	9.34187e-09
NZ_CP023992.1\|WP_069864602.1\|5993190_5994804_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173868	cd08503, PBP2_NikA_DppA_OppA_like_17, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP023992.1\|WP_079258784.1\|6009998_6010412_+\|RidA-family-protein	gnl\|CDD\|100004	cd00448, YjgF_YER057c_UK114_family, YjgF, YER057c, and UK114 belong to a large family of proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	3.66386e-32
NZ_CP023992.1\|WP_099014748.1\|6006500_6007790_-\|amino-acid-deaminase	gnl\|CDD\|143492	cd06818, PLPDE_III_cryptic_DSD, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Bacterial Cryptic D-Serine Dehydratase. This subfamily is composed of Burkholderia cepacia cryptic D-serine dehydratase (cryptic DSD), which is also called D-serine deaminase, and similar bacterial proteins. Members of this subfamily are fold type III PLP-dependent enzymes with similarity to bacterial alanine racemase (AR), which contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. AR exists as dimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Based on similarity, it is possible cryptic DSDs may also form dimers. Cryptic DSDs are distinct from the ubiquitous bacterial DSDs coded by the dsdA gene, mammalian L-serine dehydratases (LSD) and mammalian serine racemase (SerRac), which are fold type II PLP-dependent enzymes. At present, the enzymatic and biochemical properties of cryptic DSDs are still poorly understood. Typically, DSDs catalyze the dehydration of D-serine to aminoacrylate, which is rapidly hydrolyzed to pyruvate and ammonia.	1.25356e-160
NZ_CP023992.1\|WP_069864583.1\|6010671_6012144_+\|permease	gnl\|CDD\|308194	pfam02447, GntP_permease, GntP family permease. This is a family of integral membrane permeases that are involved in gluconate uptake. E. coli contains several members of this family including GntU, a low affinity transporter, and GntT, a high affinity transporter.	3.96917e-124
NZ_CP023992.1\|WP_107429818.1\|6003193_6003850_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|375435	pfam17929, TetR_C_34, Tetracyclin repressor-like, C-terminal domain. TetR family regulators are involved in the transcriptional control of multidrug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. The TetR proteins identified in overm ultiple genera of bacteria and archaea share a common helix-turn-helix (HTH) structure in their DNA-binding domain. However, TetR proteins can work in different ways: they can bind a target operator directly to exert their effect (e.g. TetR binds Tet(A) gene to repress it in the absence of tetracycline), or they can be involved in complex regulatory cascades in which the TetR protein can either be modulated by another regulator or TetR can trigger the cellular response. TetR regulates the expression of the membrane-associated tetracycline resistance protein, TetA, which exports the tetracycline antibiotic out of the cell before it can attach to the ribosomes and inhibit protein synthesis. TetR blocks transcription from the genes encoding both TetA and TetR in the absence of antibiotic. The C-terminal domain is multi-helical and is interlocked in the homodimer with the helix-turn-helix (HTH) DNA-binding domain. This entry represents the C-terminal domain present in putative TetR family transcriptional regulators found in bacteria.	2.8652e-22
NZ_CP023992.1\|WP_069865530.1\|5991700_5992912_-\|pyridoxal-phosphate-dependent-aminotransferase	gnl\|CDD\|181738	PRK09265, PRK09265, aminotransferase AlaT; Validated.	0
NZ_CP023992.1\|WP_099014746.1\|6002111_6003095_-\|zinc-binding-dehydrogenase	gnl\|CDD\|176203	cd08241, QOR1, Quinone oxidoreductase (QOR). QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR acts in the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H)-binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	7.45151e-64
NZ_CP023992.1\|WP_069864592.1\|6001230_6001908_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|184958	PRK14996, PRK14996, TetR family transcriptional regulator; Provisional.	6.05719e-20
NZ_CP023992.1\|WP_069864585.1\|6009168_6010002_+\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	1.15711e-70
NZ_CP023992.1\|WP_099017065.1\|5989142_5990996_+\|phosphoenolpyruvate-carboxykinase-(GTP)	gnl\|CDD\|235256	PRK04210, PRK04210, phosphoenolpyruvate carboxykinase (GTP).	0
NZ_CP023992.1\|WP_069864600.1\|5994809_5995769_+\|ABC-transporter-permease	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.59421e-110
NZ_CP023992.1\|WP_099014747.1\|6004005_6005622_-\|D-aminoacylase	gnl\|CDD\|238622	cd01297, D-aminoacylase, D-aminoacylases (N-acyl-D-Amino acid amidohydrolases) catalyze the hydrolysis of N-acyl-D-amino acids to produce the corresponding D-amino acids, which are used as intermediates in the synthesis of pesticides, bioactive peptides, and antibiotics.	3.01835e-105

>NZ_CP023992.1|WP_079153059.1|5995825_5996680_+|ABC-transporter-permease
MRPGFAARTWRTVRSSRPAAIGLAIVAVHVVVALLAPLLTPYHPTTGDASHALLGPSADHWAGTDQYGRDVLTRVLYGGRYALGVSVTATVLTIALGAVLGCAAALRGGWLDDLLMRVLDAVLSIPAILVLLVIVTALGTGSSVIVLAIAVVCVPQVVRVVRGAALAVVPQDYVTAARARGESTWAILRREVLPNITDVVCVEFAMRASWVVLLISSLSFLGFGADPPTPDWGLMVSENRTAITVVPMASLAPIIALATMVVGLNLAADGLSKAWGVDRIREGA
>NZ_CP023992.1|WP_069864600.1|5994809_5995769_+|ABC-transporter-permease
MLTFLVRRVVAALGTLLLSSVLVFLAVQALPGDVATQVLGRDATPDAVAALRKQMGLDQPAWERYAEWIKGALHGDFGTSLVTAKPVGGEVAQHLGNSALIAVVTVLFAVTGSLVLGILAGLYRDRWPDHLISTVSLIGMSVPEFVVATVLVLAFSVTVPVLPAVVLYGPGAGVGQLLPAVWLPAASLAIVMAAYIVRMARTSVIDVMASEYVTTARLKGLSTWRVVTRHALPSALLPTLHVIALNVAWLVGGVAVVENVFNYPGIGKLLLTSVQNRDLPVIQAIALISAVVYVVCNLAADIGSMALNPRLRTRGGRIR
>NZ_CP023992.1|WP_069864602.1|5993190_5994804_+|ABC-transporter-substrate-binding-protein
MSEISHRTAHAAAGIPRRSVLTAAAAGGALGGSALLTGCSGAASASPSRAVPTRGPAGRPDRGGTLRIARPPASDAETLDPASALSAYEYLGALYNRLVRIGSDGAVAPDLAESWEPDAKATTWTFRLRRGVTFHDGRAFTSADAAYTLRHILDKATASPQAPVLSPLVDPARLRTPDAHTLIVPLKSPHAEFPSLLTHYNCYVVPEGSARSIGRTGIGTGPFRLASFTAAGPGRVTAYPDHWAGRPVLDAIDFYTVADMQARSNALLAGQVDLLSQTNLDFATARVIAASDRATIARAENAQWYVLPMLTTEKPFTDVRVRQAMKLAYDPAHILKAALQGAGTAGWDNPVPPNDPAHLAAHPAHDPEQARHLLKKAGYERLAVDLYTSAYDPIFTPMALAYQESAGRAGIRIRVRTAAADSYYTQIWMKKPLMATYWYTGRPIDQLLNQVFRGGSSYNETAWSDKEFDALLDRARREIDEHRRRELYGQAQTLVIERGGAITPMFADRLVGISRKVRGYAEHGFEFDYLHIGLKGA
>NZ_CP023992.1|WP_069865530.1|5991700_5992912_-|pyridoxal-phosphate-dependent-aminotransferase
MQVIQSTKLANVCYEIRGPVLEEAMRLEAAGHRILKLNTGNPATFGFECPPEILEDMLRNLGDAHGYGDAKGLLTARRAVMQHYQTQGIDLDVEDIFLGNGVSELIQMSMQGLLDDGDEVLVPAPDYPLWTAAVSLAGGTAVHYRCDEQSDWLPDLADIERKVTDRTKALVIINPNNPTGAVYGEETLRGLTDIARRHRLIVCSDEIYDKILYDGATHTPTAAVAPDLLTLTFNGLSKAYRVAGYRSGWLAVCGPKAHAASYLEGLTILANMRLCANMPAQHAVATALGGRQSINDLVLPGGRLLEQRDTAYDLLTQIPGVTCVKPKGALYAFPKLDPKVYKIKDDRQMVLDLLRAEKIMIVHGTGFNWPEPDHFRIVTLPAKKDLADAVTRIGNFLDGYGQP
>NZ_CP023992.1|WP_099014743.1|5991158_5991569_-|hypothetical-protein
MYEPIRTKSVHSMAELKPDFPHRSREEELDIRLAGHLTALLTVTDELRALTPDPGLDDAAERLADQAARLRDGHAPLRAAPSATESDPAHVAALHQRAHTLAGWALVVATSREDAAVTELAAERLRSHASALGLAA
>NZ_CP023992.1|WP_099017065.1|5989142_5990996_+|phosphoenolpyruvate-carboxykinase-(GTP)
MAPSNVASSLTTPSPTSHQELVSWVGEIAALTEPDQVVWCDGSEAEYDRLCAELVEKGTFKRLDSIKRPNSYYAASDPSDVARVEDRTFICSEKEADAGPTNHWKHPAEMRAIFCGEEGSFAGEQGVFRGSMRGRTMYVVPFCMGPLGSPLSAIGVEITDSAYVAVSMRTMTRMGQDVLDVLGDEGFFVKAVHSLGAPLEPGQADVPWPCNSTKYISHFPETREIWSYGSGYGGNALLGKKCYALRIASVMARDEGWLAEHMLILKLTPPRGEAKYVAAAFPSACGKTNLAMLEPTVRGWTVETIGDDIAWMRFGEDGKLYAINPEAGFFGVAPGTGEHTNANAMKTLWGNSVFTNVALTDDGDVWWEGMTEEPPAHLTDWKGNDWTPASETPAAHPNARFTVPAGQCPIIAPEWEDPKGVPISAILFGGRRASAVPLVTESFDWQHGVFLGANVASEKTAAAEGKVGELRRDPFAMLPFCGYNMGDYMAHWVKVGKNADAAKLPKIYYVNWFRKDAGGRFVWPGFGENSRVLKWIVDRLDGTAEGVESPIGVLPAPGALDTDGLDLDDASLELLLTVDKDVWREEAALVPDHLNTFGDHTPKEMWDEYHALVKRLG
>NZ_CP023992.1|WP_099014742.1|5988185_5988896_-|hemolysin-III-family-protein
MSAMTAAAPDAAVENPPGPKAAPPLPLKPMLRGWLHAGMFPAALISGVVLTALADSPRGRLACAIYTLTACALFGTSALYHRGNWGPRTAAVLRRLDHANIFLIIAGTYTPFTLLLLPHGKKQLLLWLVWAGALAGIAFRVFWVGAPRWLYTPCYIALGWAAIFFLPDFLHTGGIAVMTLIVVGGLLYSVGAVIYGTKRPNPSPRWFGFHEVFHSFTLAAFVVHYVGISLVAYQHP
>NZ_CP023992.1|WP_099014741.1|5985200_5987237_+|thioredoxin-domain-containing-protein
MPNRLAHETSPYLLQHAENPVDWWPWSDEAFEEARRRGVPVLLSVGYSSCHWCHVMAHESFEDKATADYLNAHFVSVKVDREERPDVDAVYMEAVQAATGQGGWPMTVFLTPEAQPFYFGTYFPPRPRPGMPSFRQVLEGVGAAWEERREEVRDVAGRIVEDLARRSDIALGPGAPQPPGAEDLHTALMVLTREFDAMRGGFGGAPKFPPSMALEFLLRHHARTGSEGALQMVAATCEAMARGGVYDQLGGGFARYSVDAAWTVPHFEKMLYDNALLCRVYAHLWRATGSDLARRVALETADFMVRELRTAQGGFASALDADSDDGTGRHVEGAYYAWTPEQLREVLGEADAEFAAGYFGVTEEGTFEEGASVLQLPDGERLTDASRVASVRERLLAARGLRARPGRDDKIVAAWNGLAVAALAETGAYFDRADLVEAATETAELLVRIHMDQRGRLARTSLDGTAGGHAGVLEDYGDVAEGFLALAAVTGDGAWVDFAGLLLDTVLSRFTAEDGTLFDTADDAEALIRRPQDPTDNAAPSGWTAAAGALLSYAAITGSTGHREAAERALAVVRALGPRVPRFIGWGLAVAEARLDGPREVAVVGPGDDPATRALHRAALLATAPGAVVAVGEPGSGEVPLLQDRPLLEGRPAAYVCRGFTCDAPTADVEALTAKLGG
>NZ_CP023992.1|WP_099014740.1|5981789_5985077_-|tetratricopeptide-repeat-protein
MPGSLAVLRESHRTEVERLLSRAVEEEVRRSGGRTDGGVLLGRARGALDEMAAAAAEEYGAYVRALDESSAGSRPLSSRLSRGQLGTPALAATVAAAAAFGADLTYGTSAGTALGAGVTAAVAGSAAAVVKLTASHWPAAHRQAALRNQPGGPEQLRLQWLTAVEVRGIRPFIDQHRMTAAATRQGGGSAKRSASATGQLPKLRGADRSQAARRRTVLEQSFAHLPEADGPFAGRHAQITQIAQWVRQARASTETKPTVVLLEGPPGSGRTMLAVRAAHHLHDEFRGACLVDLRGDSPEQAPLPTRDALLHLLNRLGAPRDQLLFRERSSQDQHIRRLTELYHQYLTGLPVTIVLDDARDAEQVRTLIPERSDSLVLITSRTPLSLPDDLAARVHRVEVGPLDEPGAEELLRASAEEPTGAGPYDGQSMERIAELCGRLPLALRIAGSSLGPRTPAALVTELEAYGPVGAIERALWLRYTDQQDGARRLLRRLALAGRASLGGAAAAALLDADEQEAGRHLKALGRAGLIQHVRGSRYRLHDLVRSFAHARLLDEEQPEQRTAAQERLIRSYAELADSVIRLVDGKTSTRADIFGKGAAGGHGFTSLDAALRWLDDESSFITAALRHAEGVDQAAVLHLLGALCDYCLLRGDLYRLGEISELTQAVDQGLLMRSVQWRTGIAARQLGELDQARTTLSSVVDLYFEAQHQAGAARALCSLGITLHHQGNLVEAAAKLREALGLQRAEELRGDRAWTMHALAAVERDRGGLAEALELLGEALELHQESESLHGQAWAHFQLGQACLRMGDVPRAETELRGALDAYSRTHDQRGEAWALTQLARAQLVAGEASTAADQLRQALARHRENEDARGEAWTLYYLGQALEERGDHDSAVRELERARTMFSRMRDVYGLACARHHSARVTRDLRAAQTGSLRNSGFARQLLQDARQDFRRVGVAHGEAWSCIELAVIDAGNGKAAQALELVDEAAVLFAGYGDRRGRSWARFLRCTLLPFASAGGSVIGTAVAQEELAELMREMREDGTAGDSRLEGCAEAFALVLARGVEPETGWQAWQLGMVPSRHSREVMAVLPDRPRA
>NZ_CP023992.1|WP_099017064.1|5981462_5981711_+|hypothetical-protein
MSATSTLAMTHLVPLAKDLDENKVTPGVLGFIVFAVIGAAVWLLMKSMNKHMKRVNFEEAPEPGKAPVAASAEGTKSEERTA
>NZ_CP023992.1|WP_099014745.1|5999251_6001264_+|CocE/NonD-family-hydrolase
MKYRETFDREVHVEDVWIPTRDGKTRLHARIWRPTDAETAPVPALLEYLPYRKSDWTAPRDAQRHPWYAGHGYASVRVDLRGSGDSEGVMLDEYTATELADGVDVVNWLARQPWCTGKVGMFGISWGGFNSLQIAALRPEPLKAIVTVCSTDDRYDNDVHYTGGAVLGIDMLAWAGTMLAFTARPPHPATVGEDRWLPMWRERLDALEPYLHTWLAHQERDDYWRHGSVCEDYGAIEAAVLAVGGWADPYRDTVLRLLEHLDAPVRGLIGPWSHQYPDRGLPPGPAIGFLQETLRWWDHWLKDEPTGVLDEPMLRAWINDPVPPATSYPTMPGRWVGEDAWPSPSVSWDERPLGGPDDEPVIVRSPLHTGLDAGRFFPFGNATDLPPDQREEDGRSVCFDSAPLTGRVEILGRARVRLRLDSATPRAHVIARVCDVAPDGSSTLVTRGVLNLLSRKGRERAVEWEPGTYEDVEFELNATGYAFPPGHRIRVAVSDVYWPWVWPHGERGRLTVRPGRSALLLPVRDPGADAGRPPIVFEPPEQAPPLAVTVDPPVGARPERLVTHDVATGEWVLDVDPNYGGSRTYPDGLRYEESARETYRIRSGDPLSAVASSRWTIRLRRGDWDAEVVTAVELHATAEEFIMDSSIEARANGETVVTRAWHRTTPRTSA
>NZ_CP023992.1|WP_069864592.1|6001230_6001908_+|TetR-family-transcriptional-regulator
MASHHAEDVRVTSRSERRPPRRAVAASARTRQPTEVRRRLIVEAAVPLIAERGTAAVGVREVAAAAGVSVGTVTYHFESVQEVLSEAMVLHIERYYAALSEAAAKATSGPEGLRLLIDALFTDDTDRHWRMWFDYWNAGERDQTFARGQAERYERWHEEIRALVERGRVEGEFHCEDPADFALRFSALADGLALRRLRQVPALTVADARRHLRRFVDAELRGTAA
>NZ_CP023992.1|WP_099014746.1|6002111_6003095_-|zinc-binding-dehydrogenase
MQAIQVTRFGEPGVLALTELPDPAPGPGQVAIDVTHTAVGLIDVYIRQGLYKDREGLPQPPYVPGLEVAGTVRALGEGVTGFALGEKVVALSSGDGQGGYASVFIADQASVVSTEGHSIDPALAVAAIPNALMAHVALTRAGRLSEGESVLVHGALGALSAAFPGIARQLGAARVVGTVRAERMAAAAATKLPYDTVVDSARLPDALDGEKFDVIVDPVGGLVRTRSLDLLAPSGRLLLVGNASGDWNHGIDGNRIWYGNFTVTGFNSGGYLPTHPETFAPAARAALKAVADGLADVEIETLALADAATAHQRLEDHSANGRIVLTP
>NZ_CP023992.1|WP_107429818.1|6003193_6003850_+|TetR-family-transcriptional-regulator
MHQRARSAEDKARRADDLLKAAEALARELGGVRYVTLAAVTERVGLHRTGVRRYYASKEELLLELAERSWGQWRDAIRSAAGDRTGLGPARTAAVISETLVALPVFCDLQTHVTLYLEGDVDIDRARRYKTNAFAAHDEIATTLDRASTMTIEQIADLLAAAIMLAAGLWQVSHPTPTLAALYEQEPRWGHVALDFGPRLKGLLEACAVGLDSARSDR
>NZ_CP023992.1|WP_099014747.1|6004005_6005622_-|D-aminoacylase
MDLVIRDAHVIDGTGRARYRADVGVAGGRIAAVVAEGSGARPTGRRVVDADGLVLSPGFIDMHAHSDLALLRDPDHSAKAAQGVTLEVIGQDGLSYAPVDDRTLAQIRTAITGWNGGGPGSTDIDFSWRTVGEFLDRLDHGFDGQGIAVNAAYLIPQGTVRMLVLGWEDRAATPAEVGRMKALVAEGLEQGAVGLSSGLTYTPGMYASDAELTELCRVVAAYGGYYCPHHRSYGAGALRAYEEMVTLSRESGCALHLAHATMNFDVNKGRAPELLTLLDAAIADGADITLDTYPYLPGCTTLAAMLPSWAAEGGPDAALARLRDDAEAERIRHVMEVDGADGCHGVPIDWDTIEISGVSDPALSRYIGKTVAASAREHGEAPWVTARRLLLDDHLGPTILQHVGHEENVQAIMKHPAHTGGSDGILHGAKPHPRAYGTFPQYLGRYVRELGVLTLEECVAHLTARPAARLRLPDRGQIREGYRADLVLFDPETVAAGSTFEAPRTLPTGIPHVLIDGRFIIEDGRRTDVLAGRAIRRA
>NZ_CP023992.1|WP_099014748.1|6006500_6007790_-|amino-acid-deaminase
MATDHSDQAVAALARERVDHRFKGLPPNAEGLTVGELAAERRSLFTGGFTTPVLALSAEALEHNLVAMERYSAAHGLAFAPHGKTSLAPQLFERQLAHGAWGITAAVPTQVRIYRAFGIQRIFLANEVVDAAALRWLAAELDADPDFRFIAYVDSVRGVELMDAALREAGARRPVDVVVELGGGEGARTGIRTEPECATVADAVAATGTLRLVGVAGYEGEVPKPDGERVRAWLRRLTALAADFDAAGRFEGVDEVVVSAGGSAWFDAVADVFAELPTLSRPVLKLLRSGAYVSHDDGHYRHLTPFNRVPEEGELHPAFRLWAQVVSRPEPGQAFLNAGKRDAAYDLDMPEPQLIRSARDATTRPATGLAVTALSDQHAWVTVADGTDLEVGDWVGLGLSHPCTSFDKWQLIPVAEADGTVTDYIRTFF
>NZ_CP023992.1|WP_099014749.1|6007936_6009172_+|sugar-kinase
MSPLSSVEPADGVADAGADADDVDVDVDVVCLGESMVTFVPSRPGRLADVPSFARGIGGAESNVACGLALAGHSARWISRVGMDGFGEHLVREIAATGVDTAYVQRDPYRPTGIYFRTAGERAVGSETANSGTANSGTASSETADSETADGDPAEPLAEVVYYRAGSAAAAMSPELIPRERAWSGRVLHLTGITPALSGDCRALMRELTVRAPGRPLVSFDLNYRVSLWRKGEAEQNAEPGPAVLLGLARRCDLVFVGEDEAEAVWGVRGPEAIRAALPEPEVLVVKQGGAGATAYARRPDGTDAITFEPALRVDVVAAVGAGDAFAAGFLSGTLRGLPVAERLRHGHLMAAAVLTVPGDLGAPPARERADHLVALDATRWGTLRFGPGWTDLPSPAEKWAETAAVEVTDP
>NZ_CP023992.1|WP_069864585.1|6009168_6010002_+|IclR-family-transcriptional-regulator
MSQTVDRALSILPLLAEGPANLEQVATRLGVHKSTALRLLRTLHEHGMVYRQQDQRYRLGARLFALAQEAVENLDVREIAHPHLVTLNERCGHTVHLAVYEENEVLYIDKVESRYPVRMYSRIGKPVAITVAAVAKLLLADLPEPERRALAERLTYPAYTARSTPNAAAFLKELATVREQGWATDFGGHEESINCVGAPIRGTDGRVVAACSVSAPNVVVSAEELLSLLPLVRRTADEISREYSGGGPASASVSHASQNPSQVTAETPEKRAEETSS
>NZ_CP023992.1|WP_079258784.1|6009998_6010412_+|RidA-family-protein
MTEKLQKTAITPATHTAPPAKFSHGVKKGNILQVAGQVGFGPAVPGQAPAPVGPGLREQTLQTLRNVQSVLEEGGASWEDVVMVRIYLTDTGHFAELNEIYNEFFADLKEVPAARTTVYVGLPAGLLIEIDALAVLG
>NZ_CP023992.1|WP_069864583.1|6010671_6012144_+|permease
MMFAAAPAAETPPHTGGLLALIDGTAGLLTVAALGIALLLYLIIKVRLQPFVALLGVSIAVGLAAGLSVTELFGTVQKSDAVSLIESGMGGILGHIAIIIGLGTMLGAILEVSGGAEALSARLLGLFGERRAPLAMGLTGLIFGIPVFFDVGIFVLAPIVYAAAKRSGKSILLYAMPLLAGLSMTHAFLPPHPGPVAAAGLLHVDLGWVILMGIVVGIPSVLAAWGYSAWIGNRIFVPVPQDMVEAAEESREAVAAQQRAAGTTPAEQPVSVATVLGIIGTPLVLILCATFSSVALDPSTGRSVIEFFGHPFVALTIALLLAYYLLGIRRGWSRKSLETVSTASLKPVGNILLVVGAGGVFGAVLKGSGVAQALADAFDSAGLPVIVLAWLISVVLRVAQGSATVAIVTTAGIVTPMLSEGDYSQAHLALVIMSISAGSIFASHVNDGGFWMVAKYFGISESDTLKSWTVLETVLSVAGFVVAALLSIVI

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Crispr_ID: NZ_CP023992_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_14

6268312-6268403

Orphan

Consensus_repeat	Method
GGCGCCCCCGAAGGGGCGCGGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_14

>merge|NZ_CP023992|14|6268312-6268403|CRISPRCasFinder
GGCGCCCCCGAAGGGGCGCGGGGCTGTGCCGATATGCGGCTCCGCCGCGTGGGCGCGACCAGCCACGACGGCGCCCCGGAAGGGGCGCGGGG

>NZ_CP023992|14|14|6268312-6268403|CRISPRCasFinder
GGCGCCCCCGAAGGGGCGCGGGG	CTGTGCCGATATGCGGCTCCGCCGCGTGGGCGCGACCAGCCACGAC
GGCGCCCCGGAAGGGGCGCGGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069864362.1\|6262423_6263401_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223674
NZ_CP023992.1\|WP_099014882.1\|6260179_6261307_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|236898
NZ_CP023992.1\|WP_079258909.1\|6276290_6277034_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223912
NZ_CP023992.1\|WP_099014880.1\|6255546_6257172_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173853
NZ_CP023992.1\|WP_099014886.1\|6273202_6275161_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223021
NZ_CP023992.1\|WP_069864369.1\|6259296_6260079_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP023992.1\|WP_069865491.1\|6263486_6265283_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173871
NZ_CP023992.1\|WP_079258904.1\|6261333_6262401_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|223521
NZ_CP023992.1\|WP_069864360.1\|6265360_6266365_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP023992.1\|WP_069864354.1\|6271244_6271439_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014888.1\|6278450_6279065_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP023992.1\|WP_099017084.1\|6275376_6276294_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP023992.1\|WP_099014884.1\|6268768_6270925_-\|S9-family-peptidase	unknown	unknown	gnl\|CDD\|366030
NZ_CP023992.1\|WP_099014883.1\|6266922_6268176_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368383
NZ_CP023992.1\|WP_099014885.1\|6271501_6272386_+\|N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha--D-glucopyranoside-deacetylase	unknown	unknown	gnl\|CDD\|274584
NZ_CP023992.1\|WP_093704031.1\|6258942_6259140_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099014887.1\|6277120_6278392_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP023992.1\|WP_167460033.1\|6257724_6258843_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|377658
NZ_CP023992.1\|WP_099017083.1\|6273006_6273204_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069864350.1\|6272382_6272751_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069864362.1\|6262423_6263401_-\|ABC-transporter-permease	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.20118e-96
NZ_CP023992.1\|WP_099014880.1\|6255546_6257172_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	4.29586e-115
NZ_CP023992.1\|WP_099014886.1\|6273202_6275161_+\|hypothetical-protein	gnl\|CDD\|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	8.29046e-14
NZ_CP023992.1\|WP_099014882.1\|6260179_6261307_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	4.85648e-149
NZ_CP023992.1\|WP_069865491.1\|6263486_6265283_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173871	cd08506, PBP2_clavulanate_OppA2, The substrate-binding domain of an oligopeptide binding protein (OppA2) from the biosynthesis pathway of the beta-lactamase inhibitor clavulanic acid contains the type 2 periplasmic binding fold. Clavulanic acid (CA), a clinically important beta-lactamase inhibitor, is one of a family of clavams produced as secondary metabolites by fermentation of Streptomyces clavuligeru. The biosynthesis of CA proceeds via multiple steps from the precursors, glyceraldehyde-3-phosphate and arginine. CA possesses a characteristic (3R,5R) stereochemistry essential for reaction with penicillin-binding proteins and beta-lactamases. Two genes (oppA1 and oppA2) in the clavulanic acid gene cluster encode oligopeptide-binding proteins that are required for CA biosynthesis. OppA1/2 is involved in the binding and transport of peptides across the cell membrane of Streptomyces clavuligerus. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	2.2897e-144
NZ_CP023992.1\|WP_079258904.1\|6261333_6262401_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	7.32498e-179
NZ_CP023992.1\|WP_069864360.1\|6265360_6266365_-\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.22834e-82
NZ_CP023992.1\|WP_099014888.1\|6278450_6279065_+\|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].	5.0687e-62
NZ_CP023992.1\|WP_099017084.1\|6275376_6276294_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.61392e-70
NZ_CP023992.1\|WP_099014884.1\|6268768_6270925_-\|S9-family-peptidase	gnl\|CDD\|366030	pfam00326, Peptidase_S9, Prolyl oligopeptidase family.	3.0024e-46
NZ_CP023992.1\|WP_099014883.1\|6266922_6268176_+\|hypothetical-protein	gnl\|CDD\|368383	pfam05308, Mito_fiss_reg, Mitochondrial fission regulator. In eukaryotes, this family of proteins induces mitochondrial fission.	1.68805e-07
NZ_CP023992.1\|WP_099014885.1\|6271501_6272386_+\|N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha--D-glucopyranoside-deacetylase	gnl\|CDD\|274584	TIGR03445, mycothiol_MshB, N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase. Members of this protein family are N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase, also called 1D-myo-inosityl-2-acetamido-2-deoxy-alpha-D-glucopyranoside deacetylase, the MshB protein of mycothiol biosynthesis in Mycobacterium tuberculosis and related species. [Cellular processes, Detoxification].	3.97952e-136
NZ_CP023992.1\|WP_069864369.1\|6259296_6260079_+\|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.	0.000168205
NZ_CP023992.1\|WP_167460033.1\|6257724_6258843_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|377658	pfam06441, EHN, Epoxide hydrolase N-terminus. This family represents the N-terminal region of the eukaryotic epoxide hydrolase protein. Epoxide hydrolases (EC:3.3.2.3) comprise a group of functionally related enzymes that catalyze the addition of water to oxirane compounds (epoxides), thereby usually generating vicinal trans-diols. EHs have been found in all types of living organisms, including mammals, invertebrates, plants, fungi and bacteria. In animals, the major interest in EH is directed towards their detoxification capacity for epoxides since they are important safeguards against the cytotoxic and genotoxic potential of oxirane derivatives that are often reactive electrophiles because of the high tension of the three-membered ring system and the strong polarization of the C--O bonds. This is of significant relevance because epoxides are frequent intermediary metabolites which arise during the biotransformation of foreign compounds. This family is often found in conjunction with pfam00561.	5.92115e-61
NZ_CP023992.1\|WP_099014887.1\|6277120_6278392_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.03871e-49
NZ_CP023992.1\|WP_079258909.1\|6276290_6277034_+\|ABC-transporter-permease	gnl\|CDD\|223912	COG0842, COG0842, ABC-type multidrug transport system, permease component [Defense mechanisms].	3.34515e-11

>NZ_CP023992.1|WP_099014883.1|6266922_6268176_+|hypothetical-protein
MGQGRILNSGGRLFGALVCAVLGLISLAWIIRDLGKADESSHLWWTWAGLPFRATGGIFGSSLLDLVLLLVYAVVGLTALRSPAAAGALGSVAVVTVAVRLPSLWNLNSDWLQGIPGDLKTRANLSAWAQVVLAGLLLAVVAAARRPADLAPPGRPVSPADRPPGRPSPGAAVIGALFLGAVGAVIAAWQIYWAQERGWEIYKYLLTGKHTLPTLLSAPGAWTAWAAVALCLAATAAALARAPLARPLGMTAAALVTATGISEASLYIKLDYVDHLSDLPTVGVLSVLTGFFEAVAGLIALIALARRSVEEDTESLGGVGGPPPYAAYAAYGGQGPGSYDAQGPGGYDGAYGGQRPGGYGSGGSGGYGDGGYGGGGYGSGGYGPPPPSTPPLVPPPPGAPPTPPPPPSTPPAPPPGW
>NZ_CP023992.1|WP_069864360.1|6265360_6266365_-|ABC-transporter-permease
MTSPSQTGVVEKTAPGAEGGAPAGLAPRQLMWRRFKRDRTGVISACVVVFFFAVAVLAPVISALYGKDPYTTYGLDRPELLDPLTGYPMKPNGGIDGEFWFGIEPKLGRDVLTQLVYGIRTSLLIGLAATVLSTLTGIVIGVVAGYMGGRTDYFLGRLIDLLLSFPQQLFFVAFMPVVTALFVSPQKETPTYFRVTALVMVLWLLGWMQLARLLRGQVLSLREREFVEAAKVTGASPWRIVRKELLPNLGTPILVQSTLMLPNFVTTEAALSFLGVGVVEPTPDWGRMFAKGANFYEGDITYMFFPGIAMVVFVVAFNLLGDSVRDAMDPKTTR
>NZ_CP023992.1|WP_069865491.1|6263486_6265283_-|ABC-transporter-substrate-binding-protein
MEERSKNSRRARTYAVALAAGALALAGCSSGGGGSDPKDSNEPKMESQDITLGTAADSTGPAKDLAGAKKGGTVTVLQRDAFEHLDPGQIYVSDELIMQTLYNRTLTNYQFDDKTGKAKLVGDLATDTGKSSDGGRTWTYTLKDGLKYEDGSPITSKDVRQAVERLYAPYQTNGPTYLQQWLSGEGQKYRKALPDGPYKGKHLPKSVLDTPDDKTVVFHFDQPRAEVPFAVAMPNIGAVPPGKDTKEKYDKAPLASGPYKIRNFKPGKGIQFVKNDQWDPKTDSIRHQYVNTFDVSFGHQWVDSTRRLQADKGADRNGMTWTNAVDPSQISTVLKDKEAMSRSLTETQPYVDVVSINTDRIKDKKVREAIAWAFPSGQYLQQFGGPKAGEIGGGLVGPTLKGYDPSFDPFQKKKYPGGNAKKARELLKEAGKENYELVYAYGNGDTHQDASVVVERALERAGFKVEKKEIDQSTYYTQIGKVKNKYDLYRSSWGADWPSASTVVPPLYDGKNVYDDSANYSHLNVPSVNAEIGKVAKVSDLSRATSEWIKLSEKILSDEIPAVPTFYNRLFTLWGSGIGGVKFNSVYGAVDPTAVFIK
>NZ_CP023992.1|WP_069864362.1|6262423_6263401_-|ABC-transporter-permease
MFRFLARRSLGAIVILILISAITFFLFFALPAEPARLACGKNCDPTSLAMINKNLGLDQPVPVQYWKFMVGIFAGRDFAVGHCDAPCFGYSFVSQEPVWGTIVDRFPTTLSLALGGAAVFLVCGIGIGMIAAWRRGTWIDKFFSSLSLLGASMQIYFVGVLALAWFVSGLGIMDQPAYYPFTDNPAKWFSGMLLPWVVLSLIFMANYSRMTRSQMVEQLQEDHVRTARAKGLSSRTVFFRYAWRGAIAPIITIFGIDLGSLLGGAMVTEYTFTLHGIGRLAVESVQLTDLPMLMGVMLVSSAAIVVFNILVDAAYAFIDPRVRLA
>NZ_CP023992.1|WP_079258904.1|6261333_6262401_-|ABC-transporter-ATP-binding-protein
MTTLTKPDDGGTPPEAGPGAFLSVRDLYVRFATEDGTVKAVDGLSFDLERGRTLGIVGESGSGKSVTNLTVLGLHDPRTTTVSGEILLDGQELTGAPERTLERLRGNTMAMIFQDPLTALSPYYTVGRQIAEPYRKHTGASKSEARSRAIEMLEKVGIPNPRLRVDDYPHQFSGGMRQRAMIAMSLVCDPDLLIADEPTTALDVTVQAQILDLLRDLQQEFGSAIILITHDLGVVANTADDLLVMYAGRAVERGTVREVLRAPQHPYTWGLLGSMPRLSSDVDEPLSPIPGSPPSLLSPPPGCPFHPRCRYTDQVAGDRCATERPVLPDGRGAACHLGAERKQTLFTEQIKPRLG
>NZ_CP023992.1|WP_099014882.1|6260179_6261307_-|ATP-binding-cassette-domain-containing-protein
MSIESGIPEPLLVTEKLTKHFPIMGGFPFKRKVGAVQAVDGIDLTVHAGESFGLVGESGCGKSTTGRLLTRLLEPTGGTITYRGRDITHAGRKELAPIRSEIQMIFQDPYSSLNPRQTVGAIISGPMEINGIDPPGGREARVRELLEIVGLNPEHYNRFPHEFSGGQRQRIGVARALALEPKLIVADEPVSALDVSIQAQVVNLLQKLQRELGIAFLFIAHDLAVVRHFSQRVAVMYLGKVVEVGDRDAIYRRPRHPYTHALLSAVPDAAVVMAEDTENDPDSLRRERIRLAGDVPSPINPPSGCRFRTRCWKAQDKCAREEPPLIRLDGNGEGHLAACHFPEDPTLEAREEDVVLDPALIAAESGTEAPPRKEP
>NZ_CP023992.1|WP_069864369.1|6259296_6260079_+|GNAT-family-N-acetyltransferase
MPQNDLQRARDFRLSFARRQAGEVREVPGGFLVLHREYARSHEHNQLHIVGPADPEGLPALADEAMAFLPHRRITVHDETLGPLCAPALERAGYSHVTEVLMVHTGPVPEAAAADVVERDLGPDPYGPLRRALTAQQRRWMPDADERTVHDLVERRTARRAGAEDVLFLAAHDDSGEIASWADLYLEPAAGIAQIEEVATAEPYLRRGYADAVLTAALRRAAAAGCALRFLVADQDDWPLRWYGRRGFTAVGRAHSFSRF
>NZ_CP023992.1|WP_093704031.1|6258942_6259140_+|hypothetical-protein
MTPVQVDWLSIVFGPLALIAFALAFSAQRSASKRGESMPGWGKTVQGVGMGLVLFVAFSNMMWGG
>NZ_CP023992.1|WP_167460033.1|6257724_6258843_+|alpha/beta-fold-hydrolase
MHPFRIDVPQPDLDDLRQRLERTRWPERLPGAGWSDGASLDHVRELAAYWATGFDWRAREARLNAFPQFTTEIDGQRTHFLHVRSPEPAALPLLITHGWPGSVAEFTEVIGPLTDPRGHGGDPADAFHVVIPSLPGFAFSAPPREPGWGIRRIATAWTELMRRLGYERYGTQGGDFGSLISPEVARVAPSRVVGVHVNALVTVGSADPAGPADLTPAERSRLAGSQRWHRELSGYAAIQGTRPQTLSYGLADSPVGQLAWNVDWFAAHGDKPGALDRDAVLTNVSLYWFTNTAGTSARLYKEAASAWGTPPERSGVPTGVAVFRGDTAIRRLAEPSHAITHWSEFETGGHFAAMEVPDLLVDDVRTFFRDLR
>NZ_CP023992.1|WP_099014880.1|6255546_6257172_-|ABC-transporter-substrate-binding-protein
MPRTALRAVTAATALVAVTALTACGGGDGGADAGVIRSSWGDPPNPLEPANTNDVQGGKVLDMIFRGLKRYDPKTGEAKNALAERIESPDQRNYTVTLKKGWRFANGEKVTAASFVNAWNYGARIDHQQRNAYFFEYIEGYDKVHPATGGAPTAKTLSGLRVRNERTFTVRLTQKFSTWPKTLGYNAYVPLPRAFFEDHAGWLRKPIGNGPYQVRSYTRGSVMELRAWRGYPGPDKARNKGVDLRVYTDSNTAYTDLQAGNLDLVDDVPAQQLKFVRSDLGDRYINQPAGIIQTLTFPMYDRAWSGPAKAGLRRGISMAINRAQITERIFHGTRTPATDWTSPVLRHQGGYQQGLCGDACRYDPVRARKLIKAGGGLPGGRMTITYNADTGSHKEWVDAVCNSVNTVLRNDRACVGKPVGTFADYRNKVAGKKMTGPFRAGWQMDYPLIQNFLQPMYYTGASSNDGHFSDTGFDRLVNQANAASADGRAIAGFRDAEKILAQQMPAIPLWYQNGSAGYSQRLSEVALNQFSVPVYARIRVG
>NZ_CP023992.1|WP_099014884.1|6268768_6270925_-|S9-family-peptidase
MTGQLSFPRQHARTQRFTLGAPRALAVAPDDSRVVFLRSRSGTDRTGLLWVYDLEGRREYPAADPAELLGGAGEELSPEERARRERSREGSAGVVGYAVDAAVERAAFALSGRLFTTDLPAGTTHELRVPGPVVDPRPSPDGRHIAYAADGALRVTGVDGEGDRALAEPEGDTVTYGLAEFIAAEEMDRSRGFWWSPRSDALLAARVDEAPVKRWWIADPAHPGREPAAALYPATGTANAEVRLVLLGLDGSRTEIEWDRENYPYLARVHWSAYGPPLLLVQARDQRSQLYLAVDTGTGRTSTVHVDEDAVWLDLFPGVPAWTEDGRLVRIADEGGARVLMVGDRKLTSSALHVRAVLDIGSDDVLFSASPGAGAPLPERPGEIDVHRAWFRGSGDQGGWEPVGRRPFPAVHSAVRGGEVIALSYTGVERPGVSVEILRPADHGAAERLGELDSYAERPVITARPELVFAGKRDIPCAVLLPSGHREGDGPLPVLMDPYGGPHGQRVVASHNAHLTSQWFADQGFAVIVADGRGTPGRSPAWEKAVRDELAAVTLEDQVEAVTALAERYPLDLGRVAIRGWSYGGYLAALAVLRRPDVFHAGVVGAPVTDWRLYDTHYTERYLGLPDEQPEVYAANGLVTDEGLSGAAGTARPMMIIHGLADDNVVAAHTLRLSSALLAAGRPHEVLPLSGVTHMTPQEQVAENLLLLQVDFLKRSLG
>NZ_CP023992.1|WP_069864354.1|6271244_6271439_+|hypothetical-protein
MALSISMSVLLLIIVFMLVNKAGLKAVHAVVCVLLGFYLASSSVAPTIDDLTTNVADMIGGVKI
>NZ_CP023992.1|WP_099014885.1|6271501_6272386_+|N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha--D-glucopyranoside-deacetylase
MTVLPARRLLLVHAHPDDESINNGATMAKYAAEGAHVTLVTCTLGEEGEVIPPALAHLAADRDDALGPHRIGELATAMDALGVEDHRFLGGPGRYRDSGMMGVPQNDRPGCFWQADLDEAAGHLVAVVREIRPQVLVAYDTNGGYGHPDHIQAHRVAMRAVGLAADPDFRPDLGEPHDIAKVYWNCVPRSAVEEGFARLRAAGRDSLFPGVASVEDVPGVVADTEVTAAIDGTAHAAAKAAAMRAHATQIAVDGPFFALSNDLGQPMFIHEHYRLVKGEAGADREDDLFAGVTA
>NZ_CP023992.1|WP_069864350.1|6272382_6272751_+|hypothetical-protein
MTAPRLGGYVLLAVAGVLVGTAGALVQGAWFPGGLLLALLAVVGLCYGGVKVMGARMGGGVPAGAWTVAVLLLTSARPEGDFLFGAGLGSYAFLLGGMFLGVMCATLPLVPQPPGPPVRLGK
>NZ_CP023992.1|WP_099017083.1|6273006_6273204_-|hypothetical-protein
MTTGGMGRDPGMLILIRVVSVVSVFGSSGLAAARARPSSAAPCGASCAGLGEGYWRDPYGGVPDG
>NZ_CP023992.1|WP_099014886.1|6273202_6275161_+|hypothetical-protein
MRTPVAEDGVPAPRSGGDDDAPERTSALPRVDFPPTPERGVPAEPGGAMEPSEPREKKGGKGDGERTSDWFAPRRPRGGSSATGATPKPPASPAPDTTQGFPAPDVTQGFPSPETTQGFPAPDTTQGFPAPDPTQGFPSPETTQGFPAPQQGGGPVADLPYFTDAQSPSGHPEPTGPTTGPVTGDMYLPPSAPGGGPRDSDLLAPPGPGPASGPFGGDPQTPTGGVGPLGGGGPAAQPPTPPGGSPLSGSLGATTGVGPLNTPADGPSLFRDPDPTPSGGVPPEQISSDTLVSGVPVVPSAGRAKPPSPPVPGGPGAPAPGGDSAPAPSAPKAGKPKKKGRSKVVMAGGLLFVIVGGAYAAGLVMNHADVPNGTTVLGIDIGGTSKEVAVDKLDSALGKRTTDPLTVSVDGQQKEIKPSVAGLALDTEATVRDVAGRDYNPVTVIGSLFGGTHEAEPAVTVDEEKLRDALERLAGDSGTAREGGISFTSGKAVPVYGKEGKGLDVDKAVKAVSEGFQLRAETGRNKAITLPVAVRRPSVSKAEVDRKMKSFAEPAMSDLATVQTDASHSIQFGPDKSLPKILSMRVVDGKLVEHYNLPVLKQLYGSTFDGVLLERGDGSKKPVTPEDVVSALRQALLGTTPGERVGIVGKDN
>NZ_CP023992.1|WP_099017084.1|6275376_6276294_+|ABC-transporter-ATP-binding-protein
MGAPPVVRFEKVNKSYGSVRAVTDLDLALYPGETVALLGPNGAGKSSSLDLLLGLRHPDSGRVEVFGTTPRRAIVRGRVGAMLQSGSLMEEVTVRELVGLACDLHPKGHPVDEVLERAGLAGIASRKVNKLSGGQEQRVRFAFATAGASDLIVLDEPTTGMDVASRQTFWGAMREQAKQGRAILFATHYLEEADAVADRVIVLHRGRVLADGSSAEIKAMAGARRISFELDGPIDRAALGALPALTGVEISGRTVRIRSTDADATVHAVYGLGLYPRGLEVTGLGLEQAFLAITDAATADEESAR
>NZ_CP023992.1|WP_079258909.1|6276290_6277034_+|ABC-transporter-permease
MKTLVKLEIVRTLRNRKFMFFTIVYPSALFLLIAGSADADDQVPGTRLSMPLYYMVAMASFGALTAGLMGNGERIAKEREGGWTRQLRLTPLPGRGYVAAKIAVGAVATLPSIVVVFVVAAVGKGVRLDAVWEWPALTGAIWAGSLVFAALGVAIGYLASGDAVRPLTMIIYFGLSILGGLWMPTTSYPDWLRNIGDHLPTHAYAALGQAIELGGAPHAKDVALLIGYLALFAGGAAWLYRKDTRKA
>NZ_CP023992.1|WP_099014887.1|6277120_6278392_+|sensor-histidine-kinase
MADQAEWTDGDPEHRPRGRRPLTWWADATAYDEENDQLVTIGQSPENRRQALIKLMWIGIWMAYMGAPVSDLADGHHTVPATVCGALGLLAFVTVYLVLIFRHTGRALSRRTVFGALGTICVLAVVLTLTMGGDWLVLCVYVSVAFGAVLPLRLSRWAIPLNTVCMVAVGVLVRGSHGLVSALIVPSLLGGFAMTGVRQMVRTTRALRAARATVAQLAANEERLRLARDLHDLLGHSLSLITLKSELAGRMLPGKPEQAARQVADIERVSRQALVDVREAVSGFRRPTLEAEVAGARTALAAAGIAADLSRAGTHHPDLPPDQEGALAWALREAVTNVVRHSGARRCAVTLDETGGELCLTVTDDGRGATGPHGNGLTGLAERLQLADGRLETGPGERGGFTLRALVPLSRGARAELPSQAAP
>NZ_CP023992.1|WP_099014888.1|6278450_6279065_+|response-regulator-transcription-factor
MRGVIRVLLAEDQSMVREALAALLGLEDEIEVIAQVARGDEVVAAARTHRPDVALLDIEMPGLSGIEAAAALHRAEPGIRIVILTTFGRPGYLRRAMESGADAFLVKDAPAAQLADAIRRVLRGERVIDPTLAAAALVDGASPLTEREREVLRASGDGSTNAELARALHLSPGTVRNYLSTAIQKTAARNRAEAVRIARDKGWL

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Crispr_ID: NZ_CP023992_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_15

6718260-6718408

Orphan

Consensus_repeat	Method
GTTGAAAGCCGCACCTCTGCGCCGCGCGGGCGGAGAAGCGAACGGAGAGACGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023992_15

>merge|NZ_CP023992|15|6718260-6718408|CRISPRCasFinder
GTTGAAAGCCGCACCTCTGCGCCGCGCGGGCGGAGAAGCGAACGGAGAGACGCCCCTGTGAGCGACGCGCGAGCGGCCGCCGGGCCGCGGATGATGTTGGAAGCCGCACCTCTGCGCCGCGCGGGCGGAGAAGCGAACGGAGAGACGCC

>NZ_CP023992|15|15|6718260-6718408|CRISPRCasFinder
GTTGAAAGCCGCACCTCTGCGCCGCGCGGGCGGAGAAGCGAACGGAGAGACGCC	CCTGTGAGCGACGCGCGAGCGGCCGCCGGGCCGCGGATGAT
GTTGGAAGCCGCACCTCTGCGCCGCGCGGGCGGAGAAGCGAACGGAGAGACGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_087684298.1\|6710632_6711586_+\|methionine-synthase	unknown	unknown	gnl\|CDD\|239426
NZ_CP023992.1\|WP_069866579.1\|6711601_6713824_+\|NAD-dependent-DNA-ligase-LigA	unknown	unknown	gnl\|CDD\|236137
NZ_CP023992.1\|WP_069866557.1\|6732780_6735696_+\|EAL-domain-containing-protein	unknown	unknown	gnl\|CDD\|236645
NZ_CP023992.1\|WP_079259081.1\|6709011_6709539_+\|TIGR00730-family-Rossman-fold-protein	unknown	unknown	gnl\|CDD\|367590
NZ_CP023992.1\|WP_069866583.1\|6709682_6710372_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|181298
NZ_CP023992.1\|WP_167459942.1\|6728584_6728761_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_167459941.1\|6725301_6728439_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226415
NZ_CP023992.1\|WP_167459940.1\|6704780_6706259_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|215135
NZ_CP023992.1\|WP_099015049.1\|6730360_6731359_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381302
NZ_CP023992.1\|WP_069866577.1\|6714115_6716227_+\|bifunctional-diguanylate-cyclase/phosphodiesterase	unknown	unknown	gnl\|CDD\|238923
NZ_CP023992.1\|WP_099015045.1\|6718662_6720168_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	unknown	unknown	gnl\|CDD\|235489
NZ_CP023992.1\|WP_099017107.1\|6720858_6722349_-\|M81-family-metallopeptidase	unknown	unknown	gnl\|CDD\|377823
NZ_CP023992.1\|WP_099017105.1\|6706355_6707405_-\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133378
NZ_CP023992.1\|WP_099017106.1\|6716731_6718225_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	unknown	unknown	gnl\|CDD\|234572
NZ_CP023992.1\|WP_099015044.1\|6707408_6708770_+\|glycosyltransferase-family-1-protein	unknown	unknown	gnl\|CDD\|340817
NZ_CP023992.1\|WP_069866575.1\|6716429_6716726_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	unknown	unknown	gnl\|CDD\|178810
NZ_CP023992.1\|WP_099015046.1\|6722477_6724778_+\|MMPL-family-transporter	unknown	unknown	gnl\|CDD\|225272
NZ_CP023992.1\|WP_162502117.1\|6728875_6730069_-\|PQQ-dependent-sugar-dehydrogenase	unknown	unknown	gnl\|CDD\|369642
NZ_CP023992.1\|WP_099015050.1\|6731495_6732434_+\|2-hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240643
NZ_CP023992.1\|WP_069866565.1\|6724895_6725129_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_087684298.1\|6710632_6711586_+\|methionine-synthase	gnl\|CDD\|239426	cd03310, CIMS_like, CIMS - Cobalamine-independent methonine synthase, or MetE. Many members have been characterized as 5-methyltetrahydropteroyltriglutamate-homocysteine methyltransferases, EC:2.1.1.14, mostly from bacteria and plants. This enzyme catalyses the last step in the production of methionine by transferring a methyl group from 5-methyltetrahydrofolate to L-homocysteine without using an intermediate methyl carrier. The active enzyme has a dual (beta-alpha)8-barrel structure, and this model covers both the N-and C-terminal barrel, and some single-barrel sequences, mostly from Archaea. It is assumed that the homologous N-terminal barrel has evolved from the C-terminus via gene duplication and has subsequently lost binding sites, and it seems as if the two barrels forming the active enzyme may sometimes reside on different polypeptides. The C-terminal domain incorporates the Zinc ion, which binds and activates homocysteine. Side chains from both barrels contribute to the binding of the folate substrate.	5.67876e-66
NZ_CP023992.1\|WP_069866579.1\|6711601_6713824_+\|NAD-dependent-DNA-ligase-LigA	gnl\|CDD\|236137	PRK07956, ligA, NAD-dependent DNA ligase LigA; Validated.	0
NZ_CP023992.1\|WP_069866557.1\|6732780_6735696_+\|EAL-domain-containing-protein	gnl\|CDD\|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	4.88845e-72
NZ_CP023992.1\|WP_079259081.1\|6709011_6709539_+\|TIGR00730-family-Rossman-fold-protein	gnl\|CDD\|367590	pfam03641, Lysine_decarbox, Possible lysine decarboxylase. The members of this family share a highly conserved motif PGGXGTXXE that is probably functionally important. This family includes proteins annotated as lysine decarboxylases, although the evidence for this is not clear.	1.12096e-38
NZ_CP023992.1\|WP_069866583.1\|6709682_6710372_+\|SDR-family-oxidoreductase	gnl\|CDD\|181298	PRK08219, PRK08219, SDR family oxidoreductase.	9.10752e-109
NZ_CP023992.1\|WP_167459941.1\|6725301_6728439_+\|AAA-family-ATPase	gnl\|CDD\|226415	COG3899, COG3899, Predicted ATPase [General function prediction only].	3.23472e-36
NZ_CP023992.1\|WP_167459940.1\|6704780_6706259_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|215135	PLN02244, PLN02244, tocopherol O-methyltransferase.	1.16431e-21
NZ_CP023992.1\|WP_099015049.1\|6730360_6731359_-\|aldo/keto-reductase	gnl\|CDD\|381302	cd19076, AKR_AKR13A_13D, AKR13A and AKR13D families of aldo-keto reductase (AKR). Schizosaccharomyces pombe aldo-keto reductase YakC is a founding member of aldo-keto reductase family 13 member A1 (AKR13A1). It catalyzes the reversible reduction of ketones to the respective alcohols using NADP(+) as a hydride donor. Rauvolfia serpentina PR is a founding member of aldo-keto reductase family 13 member D1 (AKR13D1). It catalyzes the NADPH-dependent reduction of the aldehyde perakine to yield the alcohol raucaffrinoline in the biosynthetic pathway of ajmaline in Rauvolfia, a key step in indole alkaloid biosynthesis. This family also includes Arabidopsis thaliana aldo-keto reductases, ALKR1-6.	1.28432e-130
NZ_CP023992.1\|WP_069866577.1\|6714115_6716227_+\|bifunctional-diguanylate-cyclase/phosphodiesterase	gnl\|CDD\|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	1.9851e-100
NZ_CP023992.1\|WP_099015045.1\|6718662_6720168_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	gnl\|CDD\|235489	PRK05477, gatB, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB.	0
NZ_CP023992.1\|WP_099017107.1\|6720858_6722349_-\|M81-family-metallopeptidase	gnl\|CDD\|377823	pfam07364, DUF1485, Metallopeptidase family M81. This is a family of proteobacterial metallo-peptidases.	1.59507e-120
NZ_CP023992.1\|WP_099017105.1\|6706355_6707405_-\|MerR-family-transcriptional-regulator	gnl\|CDD\|133378	cd00592, HTH_MerR-like, Helix-Turn-Helix DNA binding domain of MerR-like transcription regulators. Helix-turn-helix (HTH) MerR-like transcription regulator, N-terminal domain. The MerR family transcription regulators have been shown to mediate responses to stress including exposure to heavy metals, drugs, or oxygen radicals in eubacterial and some archaeal species. They regulate transcription of multidrug/metal ion transporter genes and oxidative stress regulons by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	9.79234e-24
NZ_CP023992.1\|WP_099017106.1\|6716731_6718225_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	gnl\|CDD\|234572	PRK00012, gatA, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA.	0
NZ_CP023992.1\|WP_099015044.1\|6707408_6708770_+\|glycosyltransferase-family-1-protein	gnl\|CDD\|340817	cd03784, GT1_Gtf-like, UDP-glycosyltransferases and similar proteins. This family includes the Gtfs, a group of homologous glycosyltransferases involved in the final stages of the biosynthesis of antibiotics vancomycin and related chloroeremomycin. Gtfs transfer sugar moieties from an activated NDP-sugar donor to the oxidatively cross-linked heptapeptide core of vancomycin group antibiotics. The core structure is important for the bioactivity of the antibiotics.	9.77916e-56
NZ_CP023992.1\|WP_069866575.1\|6716429_6716726_+\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	gnl\|CDD\|178810	PRK00034, gatC, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC.	1.55747e-36
NZ_CP023992.1\|WP_099015046.1\|6722477_6724778_+\|MMPL-family-transporter	gnl\|CDD\|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	1.31624e-91
NZ_CP023992.1\|WP_099015050.1\|6731495_6732434_+\|2-hydroxyacid-dehydrogenase	gnl\|CDD\|240643	cd12166, 2-Hacid_dh_7, Putative D-isomer specific 2-hydroxyacid dehydrogenases. 2-Hydroxyacid dehydrogenases catalyze the conversion of a wide variety of D-2-hydroxy acids to their corresponding keto acids. The general mechanism is (R)-lactate + acceptor to pyruvate + reduced acceptor. Formate/glycerate and related dehydrogenases of the D-specific 2-hydroxyacid dehydrogenase superfamily include groups such as formate dehydrogenase, glycerate dehydrogenase, L-alanine dehydrogenase, and S-adenosylhomocysteine hydrolase. Despite often low sequence identity, these proteins typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann fold NAD+ binding form. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain. Some related proteins have similar structural subdomain but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence. While many members of this family are dimeric, alanine DH is hexameric and phosphoglycerate DH is tetrameric.	4.53917e-146
NZ_CP023992.1\|WP_162502117.1\|6728875_6730069_-\|PQQ-dependent-sugar-dehydrogenase	gnl\|CDD\|369642	pfam07995, GSDH, Glucose / Sorbosone dehydrogenase. Members of this family are glucose/sorbosone dehydrogenases that possess a beta-propeller fold.	3.39115e-91

>NZ_CP023992.1|WP_099017106.1|6716731_6718225_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA
MTDLTRLTAAEIAARIASGEVTAVEVTEAHLARIEAVDEKVHAFLHVDREGALAQARAVDEKRERGAELGPLAGVPLALKDIFTTEGIPTTVGSKILEGWIPPYDATVTKRLRDADVIVLGKTNMDEFAMGSSTENSAFGPTGNPWDLTRVPGGSGGGSSASLASFQAPLAIGTDTGGSIRQPAAVTGTVGVKPTYGGVSRYGMVAFSSSLDQGGPCARTVLDAALLHAVIAGHDPMDSTSIDEPVPDVVEAARNGSVRGMRVGVVKEFAGEGYQAGVMQRFNETVELLRELGAEIEEISCPSFDKALAAYYLIAPSECSSNLARFDAMRYGLRVGDDGTKSAEEVTALTRAEGFGAEVKRRIMLGTYALSSGYYDAYYGSAQKVRTLIKRDFENAFGRVDVLISPTTPTTAFPIGERADDPMAMYLADLCTIPTNLAGNAAMSLPCGLAPEDGLPVGLQIIAPAMADDRLYKVGAAVEAALTEKWGHPLLEEAPTL
>NZ_CP023992.1|WP_069866575.1|6716429_6716726_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC
MPGITREEVAHLARLARLELKAEELDHFAGQLDDIIGAVARVSEVADQDVPPTSHPLPLTNVMRTDEVRPSLTPQQALACAPAQEQQRFKVPQILGEE
>NZ_CP023992.1|WP_069866577.1|6714115_6716227_+|bifunctional-diguanylate-cyclase/phosphodiesterase
MKPTESAAPASRLRRAVLPALPAAAVAMAAFALGIGVFRVLDAGNALFPDGTVGWSLAVLTGIIVGHLVALGRDRWWGGTGSGAALTLAALLLYGWIPAVLVSLAVVVLVGAARRHRWRQAVLHGAVDILGVGAAALTLAAFGTTPSVERPWRTDTWDVSAIPQTALAAFVYLAVTRALLWCSLAPPGAGLPTLARTALVRQALVGIALLGIAPLIVVVAGDTPLLLPLFAVPLVALDSTLWIARVRAEEQLRDPLTGLPNRQWLLERTWTALDESERAGTRSALVLLDLDRFRSVNDTLGHLAGDRLLLQIAERLRLALPRGAEVARLGGDEFAVLLPTTDSLTSAQRSARVLVGDLGSPLDLDGLTLVLEASAGVAVYPDHALDAEGLLRRADVAMYQAKRDRSGVELYEARRDGNTPDRLGLLGDLRRALDAGDVELHYQPKVGFDGHVAGLEALVRWVHPDRGKVPPDEFISMAESSGLMPRLTEYVLETALGQVARWRADGLEVPVAVNVSPRDVHTPGFAGAVAGRLARHGVPAFALQLEITEHVLLEDPQRAADTLAGLTGHGVKMSLDDFGTGYSSLVHLRRLPVSELKIDRSFVARLAVDNEDAEIVRCTVDLAHSLGLLVVAEGVEDDETWERLRDLGCDAVQGWLVAAAMPPEEMTAWLRARGEGGWHRETAEPSSESASAEADEDADQPVT
>NZ_CP023992.1|WP_069866579.1|6711601_6713824_+|NAD-dependent-DNA-ligase-LigA
MAGEQQSKVPAEARERHARLAEQIEEHRFRYYVKDAPVISDAEFDKLMRELEAQEAEYPSLRTPDSPTQKVAGAYETEFTEVEHRERMLSLDNAFDDEELAAWADRIAKELGSGSYHFLCELKVDGLAVNLTYEHGRLTRAATRGDGRTGEDITPNVRTIAKIPNRLKGDRVPALVEVRGEVFLPRERFEELNAGLVEAGKPPFANPRNAAAGSLRQKDPKVTASRPLDMVVHGIGAREGFDIDRLSQAYELLHEWGLPTAAHFKVVDSIEGVREYIAYYGDNEHRHSVEHEIDGAVVKLDEIPLQGRLGSTSRAPRWAIAWKFAPEEVNTKLVDIRVGVGRTGRVTPYAVVEPITVAGSEVEFATLHNQDVVKAKGVLIGDTVVLRKAGDVIPEILGPVVDLRDGSEREFVMPATCPECDTPLQPAKEGDVDLRCPNGRSCPAQLRERIFYLAGRKSLDIENLGYVAAAALTQPLEPAEPPVKDEGDLFDLKIEQLLPIRSYVLDPDSGLPKRDPETGEEKVVTFFATQKGEPKKNALAMLANIEAAKERPLARIITGLSIRHVGPVAATALAREFRSLDRIAEADEEELAAVEGVGPTIAASLKEWFAVDWHREIVEKWRRAGVRLEEEGGEDEGPRPLEGLTVVVTGTLQSYTRDGAKEALQSRGAKVTGSVSKKTDFVVVGDNPGSKYDKAMQVKVPVLDEDGFGVLLEQGPDAAREVAMTPPEEAAEDSPEESGE
>NZ_CP023992.1|WP_087684298.1|6710632_6711586_+|methionine-synthase
MPGGDAREAAKTVTGSLEALPYLPELPARGPGADMIGRTAGMLAELYAHVEPSGWRISDRPGRDTRRARSWLGEDLDALEEFTQGYQGALKVSAVGPWTLAASLELRGGEVALSDPGACRDLTASLAEGVRAHLAEVRRRVPGAEVVLQLDEPSLTSVLRGSVRTASGYRTHGAVDRGVVEGALRTLVEAAGGPVVVHSCAPAVPFGLLRRAGVEGISFDLSLLTEREEESIGEAVEGGTALLIGAVPGTDAPLSDPAGSVGGVRTLWRRLGLSPETLAESVVVTPSCGLAGASPGYARAALAHCVRAARSLADNPE
>NZ_CP023992.1|WP_069866583.1|6709682_6710372_+|SDR-family-oxidoreductase
MGTHLITGAGSGIGAAVTERLAARGEELWLLARDAGRAKELAERFPGVRTVVGDLGDPDRLSWALGHQALPDRLDSLLHIAGVVDLGEVGELTPKAWNRQLAANLVSPAELTRLLLPQLRLAQGHVVFVNSGAGLRANAQWAAYAASKHGLKALADALRWEESGNGVRVTTVYPGRTATPMQVKVHQQEGKEYEAERWIAPETVATTILTVLDLPRDAEITDLQVRPRG
>NZ_CP023992.1|WP_079259081.1|6709011_6709539_+|TIGR00730-family-Rossman-fold-protein
MNICVFCSAADLDDRYTAPAREFAELIGKGGHTLVWGGSDVGLMKVMADGVQEHGGRLVGISVEFLAAKARENADEMVIAKDLAERKAQLLARADAVVIMVGGTGTLDEATEILELKKHGLHIKPVVLLNAAGFYDGLKQQFQRMEQEGFLPRPLSELVFFAENGVEAMTYLESV
>NZ_CP023992.1|WP_099015044.1|6707408_6708770_+|glycosyltransferase-family-1-protein
MRILIVTAGSRGDVAPFTGLGRRLLDAGHEVAVAAHAPFSGLVRGCGLDHRPLPGDPRELIRARGRTASPGEARAVTAAFLDRLADGVVGAVADGTDLVLTAFGPAGLSRAAGEACAVPVIGTYLAPSFATREFPLPGASGAAGGPGALGVHGVPGGPGVPGGPGAPGGPGAPGDGGLGPEGNLAAGRELLVRAGGLQAEVLTRLRARLGLPATASPEPDAEIRPVLHGFSPLVVPRPADWPSQVDVVGYWWPARPRDWQPPAELTDFLEAGPPPVFIGFGSMAPGQGERLGELVTAAVARAGVRAVVQAGWAGLTASGDDVLTVGDLPHDWLFPRTAAVVHHAGAGTTAAGLRAGVPAVAVPAMADQPFWAARLHRLGVAPRPLPLDALTAESLGAAITACVTGTALRRRAADLAEAVAAEDGAAAVLAHIGAVGRGEAGHGDRTSGEPGAS
>NZ_CP023992.1|WP_099017105.1|6706355_6707405_-|MerR-family-transcriptional-regulator
MILLGECRPGHTRTTAVAADANGSCAVEVQAAVTGGTQGGDAMGIGELAARTGLPVKTIRYYSDIGLLPESGRSPGGHRRYAADALPRLQLIQHLRALGTPIAAIAAVMAGERSLDELVTRELDAVREQLRTLTWRRATLRALDGCPEPERLRRLTLLAGVGTPEDAHDHLVRYWRWALPPGLPPRLVRAVVEGAVPVPPAAPTTAAVLAYAELRALATSGDRRRQPQPHQVGDVASFYSGVVDACALAAEALVTGCPDRRAEALGHFVGAYARIGGHDDTPAFRARLRALFRHGARAGSFSLRYWRHALVVTGETPRPSAASGQGHLAAPLAALHHQVAGLPLAADTP
>NZ_CP023992.1|WP_167459940.1|6704780_6706259_+|methyltransferase-domain-containing-protein
MATGTGFHSVRLLEAGFETVSADGSAEMLAQAFSNGLKHGDHILRVVQADWRWLNRDAHGEYDAIVCLGNSFTHLFSERDRRKTLAEFYAMLKHDGILVLDQRNYDAILDRGYSSKHVYYYCGEDVAVEPEYVDEGLVRMRYSFPDESVYHLNMFPLRKDYTRRLMQEVGFQRIETYGDFQHTYREERPDFFIHVAEKEYRTTEAPKPVGSVTGNAEYSGAVGTARDYYNSADADAFYWRVWGGEDIHIGIYDRPDEPIAEASRRTVARMAGQLGLTESSVVLDLGAGFGGSARYLAETYGCRVMALNLSEVENERHRTLNAERGLTEAIEVMDGSFESIPLPDDSVDVVWSQDAFLHSGNRARPLEEAARVLRPGGHLIFTDPMAADGCPVETLRPILDRIHLETMGSPEFYRRELARLGFTEVGGGFQEHREHLITHYARVLEETRHQEADGLAEHVSADYLTHMKKGLSNWVEGGRNCHVTWGIFHFTR
>NZ_CP023992.1|WP_099015045.1|6718662_6720168_+|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB
MTVTELVSYEDALAAYDPVMGLEVHVELGTKTKMFCGCSTALGAEPNTQTCPTCLGMPGSLPVVNAIGVESAIKIGLALNCEIAEWCRFARKNYFYPDMPKNFQTSQYDEPIAFNGYLDVDVDGEVFRVEIERAHMEEDTGKSTHVGGATGRIHGAQHSLLDYNRAGIPLIEIVTKPIVGAGAKAPEVAKAYVTELRELIKSLGVSDARMEMGQMRCDVNLSLRPQGADKFGTRSETKNVNSLRSVERAVRFEIQRHAAVLGDGGTIIQETRHFHEEDGSTTSGRVKEEAEDYRYFPEPDLVPVAPARTWVEELRGGLPELPRVRRNRLREEWGLSRHEMQSVLNAGAIELITATIDEGAPADQARKWWMGELARRANEDGVELTALPITPAQVARVCALVKEGSLNDKLARQTIEGVLAGEGGPDEVVAARGLKVVSDEGALGTAVDEAIAANAAIADKIRGGKVAAAGALVGAVMKATRGQADAARVRELILEKLGVEG
>NZ_CP023992.1|WP_099017107.1|6720858_6722349_-|M81-family-metallopeptidase
MTPAASRARRPRIGIGGMHIESSTFSPHRAAYDDFRVTRGAELLDRYAWTRPDGELTGRAEWVPLLHAVSLPGGPVERATYDRIKGELIERLRRAGPLDGLVYDIHGAMSVVGLEDAEGDLTDAVREAIGPDALISAAMDPHGNVSRRFASRLDLITAHRLAPHEDAWETRERAARKLVERLASGRGRPHLAWVQIPVLLPGERTSTRLEPAKSLYGRLAAVEAMDGVVDAAMWVGYAWADEPRCRAAVVVTGDDPVLAVEQTRSLAREYWEVRHDFAFVGPTGGADECIAEAVASCARPFLISDSGDNPTAGGAGDLAYMLGRLLANEDLAAGRATALHPGITDPAAVAACFAAGPGATVRLSVGGGISRGTADHAEPYDLTGEVVALRRNDPVGGDLAAVRRGGVTVILVSRRKPFHTRADFGELDPCGYDLVVVKIGYLEPELYDLAADWRLALTPGGVDQDLTRLGHRRIARPLYPFDDEGFEVPHLEPLLL
>NZ_CP023992.1|WP_099015046.1|6722477_6724778_+|MMPL-family-transporter
MAALARWCLRRRAIVIVLWLAAFAGVAAAAAVTGSAYSNNYDIPGTDSSKATALMEQRLPERAGDSDTIVWHTADGAGTVRGPGVERRMTEALRQVADLPGVASVAGPYGADDTSRISADQHTAYATVVFREPAADLGGAEVRQVLDTVRSAASGARGLEVEMGGEGASLTERTGPAHLSEAIGVAVAAVVLFLAFGSLAATLLPIATALIGVGTAYAAIGLLGHAMTIADFAPMLGMLIGLGVGIDYALFIVTRHRKGLRQGLSVERAAQRAVATSGRAVVFAGATVCLALLGMLVLRLSFLNGVAVAAALTVALTVAASLTLLPALLGLIGMRALSRRERRRLAERGPEAMSTQGLCARWAVLVERRPKLLGAAAAVLIAVLALPTFSLHLGTSDQGNGPSTSTTRRAYDLLADGFGPGFNGPLTLMGSIDGADDRMAFTRLPETLRTIDGVASVSAADLSGGGDTGVITVVPETAPQSRATSELVGRLRAQVLPRAEEGSSLRVYVGGLTAGYDDFAAVIVSKLPLFVGVVVALGCVLLLLAFRSIGIPIKAAVMNVAAVASSFGVVVAIFQWGWGSDLLGLGRAGPIEPFLPVIMVSVLFGLSMDYQVFLVSRMYEEWQRTRDNRTAVRVGLAETSRVINSAAVIMIAVFSAFVLSGDRIIAMFGIGLAAAVALDAFVLRTLLVPALMHLLGGANWWLPGWLERLLPRISIEGEGDGTGGGGVGAEGGGDGSPSGPASVPVALPGQAVNGSERAGTARSPVS
>NZ_CP023992.1|WP_069866565.1|6724895_6725129_+|hypothetical-protein
MDAFHETLVTRENAMLHHELHRIREAELLREAAAQRLVREAARSRGGRSAEHEGGGRVRPVRRWRGHRSSRSYRTAA
>NZ_CP023992.1|WP_167459941.1|6725301_6728439_+|AAA-family-ATPase
MLDDVHTTSVSPVFIGRAQELATLEDALARATAGEPQVLLVGGEAGVGKTRLIDEFLASAVAAGAVAAVGGCVEIGADGLPFAPVSTVLRSLRRKLGGELDGAAAGQEGELARLLPELGETARASHDEEGRARLFELTVRLLERLAAERTLVVAIEDLHWADRSTRELLGYLFRSLLSARLLVVATYRSDDIHRRHPLRPFLAEVDRMREVRRIELSRFTRVEVHAQLTGINGAEPERDLLDRIFKRSDGNAFFVEEIARSINEGCRTGLSESLRDLLLVRVEALSEEAQRVVRILAEGGSSVEYELLRAVARLGEDELIDALRAAVGANILRPTADDSGYRFRHSLVREAVRDDLLPGERSRLNRRFAEALEAEPALVRADERAARLASYWYHAHDPAKALPAVLQASVEARRRYAHAEQLRLLERALELWEDAPKEIREAQRPMDYAEVYPACGCADQALRQLDLLAEVVVAAHMSGQLERALAISKRALRTLDRSGHDPLRAAWFWTQRCKLMASLARGDGWEELSRAQELVRGLPPSPVHAEVMSQVAGWTMTHRPGPEGMAAAERAVELARLVGAESTELNARLTLAYFTVDSGDIERGLAEMREVCGRAVALGDISVLGRCYVNLTSALEGVGRSAEAVETAEEGGRILDRVGLVDSRAWLFGNLAESLFSLGRWDEAEAAALKTLRLALGTKPRGTAANRLARLALVRGDWGTAERESAATREHYGARNTEPQYTLKVAGQAIELAAARGRILEVRALLEQAVAAGFPPGMQRYLWPLLCEAAAAESAARGLPTAEPGRGEALARLRVAVKRVPQPVPVWRAHAAMLQAELERAEGRDRPALWAEATAAFAALDRPYPLARARHRWAEALLAPGRGAAPAQADREHAAELLAQAHAVADRLGARPLREEIELLARRARLPLASAATRAPLDASPPHTPALPPAPGASAAASEPAEPDHPADPAEELGLTPRERDVLRLVAAGRSNRQIAEELFISPKTASVHVSNILAKLRVSGRTEAAAVAHRLRLVDGLTDGTPAR
>NZ_CP023992.1|WP_167459942.1|6728584_6728761_-|hypothetical-protein
MFNLIEELFAPGRKHTEEERNRLEITLDETGSSDPGKGPIDLDSGRVVIRPREGDAEG
>NZ_CP023992.1|WP_162502117.1|6728875_6730069_-|PQQ-dependent-sugar-dehydrogenase
MERNPTVRRPRVTSVLAAAAAVLLMAGCSSDGDSIIRPGGRSSSPTKPDGGGSSSGAPSPKESAAPAKGSVKVVRTLTTKLKSPWGLAPLPGGDLLVSSRDTGKIFKISADTGKKTELGSVPGVSASGEGGLLGLAVSSDFGSDHMVYAYFTTDSDNRIARMVYDDRRPAGDQLGAPDTLFKGIPKGTIHNGGRIAFGPDKMLYAGTGENGDGGLAQDMDSFGGKILRMTPEGEPAPRNPDAQSVVYSWGHRNVQGLAWDADKRLWASEFGQDTWDELNQIQPGKNYGWPEAEGKADKKGFADPVEQWKPKDASPSGIAFAKGSIWMAGLRGERLWRIPLKGAKPVAKPQSFLDGKYGRLRSVAAADDGGLWLATSDTDGRGRPDRQDDRILRLEVR
>NZ_CP023992.1|WP_099015049.1|6730360_6731359_-|aldo/keto-reductase
MERRRIGAAALEVGAIGLGCMPMSWAYTASQRSGEHSVRTVHTALDSGASLLDTADMYGPFTNELLVGRVLKERRADAFVSTKCGLLVGEQHIVANGRPGYVKRACDASLRRLQTDVIDLYQLHRADPEVPIEETWGAMAELVAAGKVRALGLCAVGARAQRRTGARMHDATVRQLERVQQVFPVSCVQAELSVWSPDALEALVPWCASRGVGFLAAMPLGNGFLSGTLTPGQGFEPDDMRARHPRFTAEMMAANQPIVAGLRRVAQRHGDGVAPAQVALAWLLAQGPHVVPVPGTKRERWAAENCAAADLPLSHEDLAEIAELPPARGSWD
>NZ_CP023992.1|WP_099015050.1|6731495_6732434_+|2-hydroxyacid-dehydrogenase
MRDLVWLPIPPEEIDGLPDTLEYAHWDGGPDFPTDPARCAFYCVPYMKPPQVCTRPLPAMANLRVVQTLTAGIDHIKPALADLAPGVRLCNARGVHDASTAELALTLILASLRGIPDFVRGQDAEEWRSGFRPALADKSVLIVGYGAIGSAIEDRLVPFECERVMRVARSPRTTERGPVHPIAELPQLLPDADVVVLVTPLTEDTRGLAGAEFLSRMKDGALLVNVARGGVVDTKALLSEVESGRLRAALDVTDPEPLPTGHPLWHAPGVLISPHVGGPTSAFLPRAKRLLRDQLIRYARGESLAHLVATTG
>NZ_CP023992.1|WP_069866557.1|6732780_6735696_+|EAL-domain-containing-protein
MSATGAVLARPSVSGGAGLLPQVVLALVCGGYAAGAIVGWGSSRLALVMGDFGLSAAAFAAAASCLWHGRGHAGRLRPAWLLFAASSAMAGLGNAVWGWYEVVLGRPVPTPSVADFCFLLFAPPAIVGMLVLAKRPTSRARWICLGLDAWLIAGSLVTLSWSLALAHTGQFGGNGAFVARGALALAYPLLDIVLVSMVIVLHFRRSSGNRSAINTAIAAFALTVLCDALFTSPLLREHYRSGQILDAGWFAGSALLAYAPWVARREAAQNPPPTRRSTQQQSAPIAGSLAALAPYLAAAVCTLGVLFNVMDGRPIDGVVLLTACAVVLALVVRQAIMLMDNIRLTQELAQKESHFRSLVQSSSDVIMIAAPTGILRYVSPAASGVYGREAEELEGSELASLIHPEDLGSVVHEVRRFLAAPPGEEPTTRIECRFRSGSGDWLNVESTINRHHGGLIFNSRDVTERVRLQAQLQHNAEHDPLTDLPNRALFTRRVRHAVAGRRRTDAGTAVLFIDLDGFKAVNDTVGHHAGDELLVQAARRLQESVRSGSGDCAARLGGDEFAALIVGDGVGEAGTREQRIMEIADRLRLRLSQPYRVEGGTEVRVAASIGVAFAEPGTSPGALMRNADLAMYRAKAAGKNRVELYAPQMQAEVARRAEVATRLRAALHDGEFVLLHQPVVELASGRITAVAAQARWRSAQGILFTPAEFLRVADNGRGGGEDTARTAELSRWMLEAAVEQAAQRRRDGHPVPVCVRLPASRLVDKSMPPKAVETLLARHGLPSGALILELTDSDPRVPLDELEHRLGALRRLGVRIALDGFGSGYAAIRALRRLPIDVLKLDPGLVEGVVESSRLHKITAGLLRIAGDLGMQSIAEGVELPEQIVTLRGMGCTHAQGPAFSGPLDEHRLRRALLRGGYPVPRPEPPLLVGGALPIRHGGHVGHGGSHGPRRTEPHTHPPTRSNTETPVPPT

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Crispr_ID: NZ_CP023992_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_16

7336650-7336768

Orphan

Consensus_repeat	Method
CCGAATGCCGCACCGGGCGCCGC	CRISPRCasFinder

2 spacers

DEDDh

The CRISPR arrays of NZ_CP023992_16

>merge|NZ_CP023992|16|7336650-7336768|CRISPRCasFinder
CCAAGTCTCGCATCGGGTCCCGCGGCCAGTGTCACGTCGGGTCCTACGCCGAATGCCGCACCGGGCGCCGCACCGAATGCCGCACCGGGCGCCGCACCGAATGCCGCACCGGGCGCCGC

>NZ_CP023992|16|16|7336650-7336768|CRISPRCasFinder
CCAAGTCTCGCATCGGGTCCCGC	GGCCAGTGTCACGTCGGGTCCTACG
CCGAATGCCGCACCGGGCGCCGC	ACCGAATGCCGCACCGGGCGCCGCA
CCGAATGCCGCACCGGGCGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_099017142.1\|7341166_7342081_-\|ErmE/ErmH/ErmO/ErmR-family-23S-rRNA-(adenine(2058)-N(6))-methyltransferase	unknown	unknown	gnl\|CDD\|128898
NZ_CP023992.1\|WP_099015265.1\|7349203_7349407_-\|DUF397-domain-containing-protein	unknown	unknown	gnl\|CDD\|377231
NZ_CP023992.1\|WP_099015251.1\|7327548_7328400_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379262
NZ_CP023992.1\|WP_099015260.1\|7337821_7338703_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP023992.1\|WP_099015264.1\|7347538_7349092_-\|sporulation-protein	unknown	unknown	gnl\|CDD\|378342
NZ_CP023992.1\|WP_099015258.1\|7333916_7334639_+\|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	gnl\|CDD\|181176
NZ_CP023992.1\|WP_099015257.1\|7332864_7333689_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224044
NZ_CP023992.1\|WP_099017141.1\|7338756_7340043_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP023992.1\|WP_099015252.1\|7328523_7329129_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_069867133.1\|7345431_7346652_+\|S8-family-peptidase	unknown	unknown	gnl\|CDD\|173790
NZ_CP023992.1\|WP_099017139.1\|7335091_7335673_+\|TIGR03086-family-protein	unknown	unknown	gnl\|CDD\|274424
NZ_CP023992.1\|WP_099015255.1\|7331522_7331951_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023992.1\|WP_099015254.1\|7329675_7330926_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP023992.1\|WP_099015262.1\|7342779_7345059_-\|MMPL-family-transporter	unknown	unknown	gnl\|CDD\|225272
NZ_CP023992.1\|WP_099017140.1\|7335701_7336601_-\|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl\|CDD\|366736
NZ_CP023992.1\|WP_099015263.1\|7346772_7347369_-\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|99749
NZ_CP023992.1\|WP_099015256.1\|7332108_7332642_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099015261.1\|7340195_7341263_+\|CDP-alcohol-phosphatidyltransferase-family-protein	unknown	unknown	gnl\|CDD\|223632
NZ_CP023992.1\|WP_099015253.1\|7329125_7329317_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099015259.1\|7336877_7337825_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_099017142.1\|7341166_7342081_-\|ErmE/ErmH/ErmO/ErmR-family-23S-rRNA-(adenine(2058)-N(6))-methyltransferase	gnl\|CDD\|128898	smart00650, rADc, Ribosomal RNA adenine dimethylases.	2.05175e-61
NZ_CP023992.1\|WP_099015265.1\|7349203_7349407_-\|DUF397-domain-containing-protein	gnl\|CDD\|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	5.52968e-14
NZ_CP023992.1\|WP_099015251.1\|7327548_7328400_+\|helix-turn-helix-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.	6.53803e-10
NZ_CP023992.1\|WP_099015260.1\|7337821_7338703_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.19642e-78
NZ_CP023992.1\|WP_099015264.1\|7347538_7349092_-\|sporulation-protein	gnl\|CDD\|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	3.80101e-27
NZ_CP023992.1\|WP_099015258.1\|7333916_7334639_+\|3'-5'-exonuclease	gnl\|CDD\|181176	PRK07942, PRK07942, DNA polymerase III subunit epsilon; Provisional.	1.35163e-109
NZ_CP023992.1\|WP_099015257.1\|7332864_7333689_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224044	COG1119, ModF, ABC-type molybdenum transport system, ATPase component/photorepair protein PhrA [Inorganic ion transport and metabolism].	1.74807e-75
NZ_CP023992.1\|WP_099017141.1\|7338756_7340043_+\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.83843e-49
NZ_CP023992.1\|WP_099015262.1\|7342779_7345059_-\|MMPL-family-transporter	gnl\|CDD\|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	5.66109e-79
NZ_CP023992.1\|WP_069867133.1\|7345431_7346652_+\|S8-family-peptidase	gnl\|CDD\|173790	cd04077, Peptidases_S8_PCSK9_ProteinaseK_like, Peptidase S8 family domain in ProteinaseK-like proteins. The peptidase S8 or Subtilase clan of proteases have a Asp/His/Ser catalytic triad that is not homologous to trypsin. This CD contains several members of this clan including: PCSK9 (Proprotein convertase subtilisin/kexin type 9), Proteinase_K, Proteinase_T, and other subtilisin-like serine proteases. PCSK9 posttranslationally regulates hepatic low-density lipoprotein receptors (LDLRs) by binding to LDLRs on the cell surface, leading to their degradation. The binding site of PCSK9 has been localized to the epidermal growth factor-like repeat A (EGF-A) domain of the LDLR. Characterized Proteinases K are secreted endopeptidases with a high degree of sequence conservation. Proteinases K are not substrate-specific and function in a wide variety of species in different pathways. It can hydrolyze keratin and other proteins with subtilisin-like specificity. The number of calcium-binding motifs found in these differ. Proteinase T is a novel proteinase from the fungus Tritirachium album Limber. The amino acid sequence of proteinase T as deduced from the nucleotide sequence is about 56% identical to that of proteinase K.	5.16661e-121
NZ_CP023992.1\|WP_099017139.1\|7335091_7335673_+\|TIGR03086-family-protein	gnl\|CDD\|274424	TIGR03086, TIGR03086, TIGR03086 family protein. This family, like pfam07398 and TIGRFAMs family TIGR030834, belongs to the larger set of probable enzymes defined in family TIGR03083. Members are found primarily in the Actinobacteria (Mycobacterium, Streptomyces, etc.). The family is uncharacterized.	1.14544e-39
NZ_CP023992.1\|WP_099015255.1\|7331522_7331951_+\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.26778e-14
NZ_CP023992.1\|WP_099015254.1\|7329675_7330926_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	7.7293e-07
NZ_CP023992.1\|WP_099017140.1\|7335701_7336601_-\|aminoglycoside-phosphotransferase-family-protein	gnl\|CDD\|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	1.67599e-11
NZ_CP023992.1\|WP_099015261.1\|7340195_7341263_+\|CDP-alcohol-phosphatidyltransferase-family-protein	gnl\|CDD\|223632	COG0558, PgsA, Phosphatidylglycerophosphate synthase [Lipid metabolism].	2.89916e-15
NZ_CP023992.1\|WP_099015263.1\|7346772_7347369_-\|Uma2-family-endonuclease	gnl\|CDD\|99749	cd06260, DUF820, Domain of unknown function (DUF820). This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. They have been predicted to belong to the PD-(D/E)xK superfamily of nucleases.	3.52021e-20
NZ_CP023992.1\|WP_099015259.1\|7336877_7337825_+\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	5.76449e-79

>NZ_CP023992.1|WP_099017140.1|7335701_7336601_-|aminoglycoside-phosphotransferase-family-protein
MTEERARAVLSAALPPYRAGTAEARLLALGENAVFAVDSLSLVVRISRDLEVWDRAAHELRIADWLAREGLPAVRPDRRFGPEQPLPFANHLVTYWQRLPDPVRPAGPRDLAELLRMVHALPDPPADPAPLTLPRRDLLGGVERWLRLAGDAIDPADAAYLRARRDDFATAVEELTPRLTPGPIHGDALPRNVHIGPDGPVLVDLETFSHDLREHDLVVMALSRDRYGLGAAEYDAFVAEYGWDVREWPGCAVLRGARETASCAWVSQHAPGNPAARTEFARRIASLREGDTAVRWHTF
>NZ_CP023992.1|WP_099017139.1|7335091_7335673_+|TIGR03086-family-protein
MIDFGPAAQRVTALLSGVSDEQLTAPTPCGTYSVADLLDHFMGLAIGMRHAAEKTTAVAGPDAPAPGQGAAERLDPDWRQELPRRLDALTAAWREPSAWQGTTEAGGVTMPAQMMGIVALDEVVIHGWDLARATGQPYDCDPHCAEAIIGWLSAFPDEQRPEGAFGPIVSVADDAPPLARAVALSGRDPEWRA
>NZ_CP023992.1|WP_099015258.1|7333916_7334639_+|3'-5'-exonuclease
MGWHRGLLIGFDLETTGTDPRTARIVTAAVVEARGGEPIGRREWLADPQVPIPDDAVAVHGITNERAAAEGRPAREVVEEVAEVLVAHWRSGAPVVAYNAAFDLSLLAAELGRHGLRPLSERLEGAETGPVVDPYTIDRAVDRYRKGKRTLEAVCGEYGVVHDRAHDAGADALAAVRVACALAERHREVAGLELWDLHRKQVGWYAHWAADFQSWLRRKGTPDAVVDGGWPLREAEAAVG
>NZ_CP023992.1|WP_099015257.1|7332864_7333689_-|ATP-binding-cassette-domain-containing-protein
MTAPAVPVLKLSDVDVVRDGTPLLRSISLTVHQGEHWALLGSNGAGKSTLLSLAGALVHPTHGTVEVLGRTLGRVDLRELRSFVGHVDPRHPLRSPLRVRDVVLTGLTNTVEPVPRRRPTAEQRDRADRLLTTLGMGGKLDARWPTLSQGQRGRVLIARALMPRPRLLLLDEPATGLDLAAREQLLESLDTLRRDHPELATVLVTHHLEELPASTTHAMLLRTGECLASGAVDEVVTTDHITKCFDHPVHITRTDGRWTARTIRRIRTDPGKRV
>NZ_CP023992.1|WP_099015256.1|7332108_7332642_+|hypothetical-protein
MSRVALATLLPEQPIGLRRADEHWNAVAVPTTWSRLVLASLAGRNGAVFEDARFRHLVWVIPSGGADEWPEPSGMGVIVYRTGEQLAVPGLGGFHGSHWLRTPSGQLLFTDPDELRTAVEKVAGPLADAERLGPMVVCSYCDTPTRDSKIINTWTSPCDGSVHNDYACRGCDSTRGR
>NZ_CP023992.1|WP_099015255.1|7331522_7331951_+|ATP-binding-protein
MTATARPSAVGVPAYSQVLLREPGAAALARRMVRTVLDTWHLPHLADEAAQVTSELVTNVVDHARGGSMRLSLTRVSEYRVRLAVTDKSRNEPVRKTPSPGEERGRGLAVVDAYSAAWGVDLLPWGKRVWCELEAGAGEDQR
>NZ_CP023992.1|WP_099015254.1|7329675_7330926_+|helix-turn-helix-domain-containing-protein
MSSDATSDPLDHPLVFGQRMQVLRTRRGMSRTVLAGLLDKSPSWVKQIENGTLHTPGLPMILRIAEVLRVRDLAELTGDQSLPIDLFIGPGHAKLPAVRAAIDAFPLAADREAPSPAYLSARLESAWAARHSAPNHREVIGGLLPVLLRDAQLAVRQADRAAERRAAQAVLAEVYSLSQFFIAYQPDSALLWRVAERGMVAAQESEDPHAIGVAAWLAAQAHRDSGPAHFEAADAVTLETLRYLTPLLPDATDDVRAIAGALRFEAGYTAACRGDTGTAWGYWDTAGKVAERLPADYYHPVTSFSRAIMGAHAVTVAVELRAGGESVRQAAKADSKTIRSRPRRARHRIEEARGYQLDGQSETALAALDKAFEAAPETIRYNGYARRIILEETESKSPAHRRRAAELAVKIGMLAA
>NZ_CP023992.1|WP_099015253.1|7329125_7329317_+|hypothetical-protein
MMAPEQTSEEAKGSFTDQAWRMAIGHAAGCLVCRMSGVECETGGQLLGAYEEAIREARAEEIA
>NZ_CP023992.1|WP_099015252.1|7328523_7329129_+|hypothetical-protein
MATSSAQAFPWAPPNAMDVEALPVGEWWDAVSAPTSVADRALELLGDRSGAVIQDDTYGKTYWLIGIDTARSWCVRQVRVLTALADEGTLLGVPPVSWGPEHRTHWRIPLGPDRYLTDTNRLARALRRAVDEVLGPAPDGRQLCYRCQLPTDEPVPVAIEHSGSVARATVYACPAHAGDYSRDTVAQAAARRRAREFGRSR
>NZ_CP023992.1|WP_099015251.1|7327548_7328400_+|helix-turn-helix-transcriptional-regulator
MPASPSSSAEAARKALAARLRDLRLDAELTVRELADRAGWSHSKVSRIENVRTAPSPEDIRAWARACGADGQAEDLVAALRTVEGMWIEWRRMERRGLRKAQESVRPLYERTRAFRAYDSWLVPGLLQTMGYTTAILHATRKRRGLVDDVDAAVAERMDRQHVLYEGRHTFAFLLEEAVLRAGIGGREVMREQLRHLLTVGFLPNVSLGIVPMQPSREAMRPVEGFWIFDNAQVAVELVSGYLTISQPQEIEMYAQVFRDLGNLAVYGEKARTLIHEAIAALG
>NZ_CP023992.1|WP_099015259.1|7336877_7337825_+|sugar-ABC-transporter-permease
MVPVTAASAHSGEGSAEHPSAAPGKRPGSRVAAHRHGTWFLVLPALIPILLLSVGPLLYGIALAFTDSQAGRTEPTQWIGLLNFQDLLRDTLFWESFRIGLVWAVAVSVPQFLLALGLALLLNQNLRFRWLARALAIVPWAMPEVVVGIMWRLVYHPDAGLLNETLGIHRDWLGSLSTALPAVVVVGIWANLPQVTVTLLAGLSHVPRELHEAAAMDGAGAWRRFRAVTWPAIRPIALAISALSFIWNVNSFALVYVLTGGGPGGRTRLPMLFAYEEAFRYGQFGYAAAMGCVLVAVVSILLAVHLVARLKGDDA
>NZ_CP023992.1|WP_099015260.1|7337821_7338703_+|carbohydrate-ABC-transporter-permease
MSPRATAGRRAARTTTAGRHAARTGQYLALLGYMVFLAFPLLWLVSTAFKPPRELASLHPGWIPDHPTLDNFRQAFEEQPLLRSAGNSLIASLAAAAITVVIATPMAYVMARHHRSRLSRAATGWIVVSQAFPFVLVIIPLFLVLKEVRLIDSLTGLIMVYVVWSLPFALWMLAGYARAVPRELEEAAAVDGAGRLRTLISVTVPLLAPGIVATALFAFLTAWNEFFFALVLLKSPRKQTMPVILTHFIGTEGVADLGPLAAASLLATLPSLVLFAVIQRRITSGTLAGAVKH
>NZ_CP023992.1|WP_099017141.1|7338756_7340043_+|extracellular-solute-binding-protein
MRRRTLLAASATGTLLSACAPERRRATGGRITLRFQSLAWQKESVAANKQLVGEWNAAHPDIRVEYVQGSWDAVHDQLLTSFEGGEAPDIIHDATDDLADFAYGGYLADLTDLLPRRLKAEIPARTWQTATFGGGVHGVPFLQEPRVLIANRALLERARVRIPTPQRPWSWAEFEDAAGELTRDGTYGVAWPLKEPVSATLNLSLSTGGKVFHRGADGKVTVRFDAADQWVPRVIHDQLGGDRSAARTTLGMGGSDTLPGFFGGKYAMVPLGFSYRQQIVQQAPEGFAWTVLPSPAGPGGDQRQGVSPQTLSIAADSPYRREAVRFIDFFLRPPHMVRLARGDWMLPTGVTALRDPALRTRRHGWATGAALAGRLRPAPAQSVRGYPEWKDKVATPALQEYYSGAIGMAELRKRLVEDGNLVLARYQR
>NZ_CP023992.1|WP_099015261.1|7340195_7341263_+|CDP-alcohol-phosphatidyltransferase-family-protein
MPRDIPPLAEVRRITEKKRDAWWTVMLVDPVATPLVRWTARYTRATPNQLTWGAFLVGLGSAACFAQGDWRWLLLGAVLYHVSFIFDCMDGKLARLTGTGSVFGAWLDFVFDRIRVLVCSIALMGGQYARTDDVLYLWLALAVASLDALRYIDSLEIFKIRHGMRKQIKARMRAARKAENQAELAFMEDLLRENPEADLETDRDTVAPLEPVAAVEVTAAPGTPAATGTDAPAGTDALAGAETPVQVPTPRRPAVVDLHQEFRRRFPWWVRCRNFLQRHRIRAHLISGIEFQMGVFIIGPALDAVVATTVVSGALLLVFELAIIYKLLLSTRDFTRTINSFETADRFPATTSVNS
>NZ_CP023992.1|WP_099017142.1|7341166_7342081_-|ErmE/ErmH/ErmO/ErmR-family-23S-rRNA-(adenine(2058)-N(6))-methyltransferase
MEARRTEARRTEARRTEPRRTERDRARRTYGQNFLADPGTVARVVRAARPGPGDLLVEVGAGKGALTEALAPRCRELISYEIDRHLIPGLRERLARHPRVRVVHRDFLTAAPPREPFALVGNVPYARTAEIVAWALRAVPRLTSATLLTQAEYARKRTGDYGRWSLLTVRSWPEVEWRLCGLVDRTAFRPVPAVDGGILRLTRRPQSLLTDPVTRSAYADLVELGFTGVGGSLHASLRRVCPTRAVDRAFRAAGLGREVVVAYVAPEQWLVLAQELTEVVAGKRSAVSKELMVRVKSRVDNSNL
>NZ_CP023992.1|WP_099015262.1|7342779_7345059_-|MMPL-family-transporter
MADTGRLERPRGIAARAGSWSARHRWAAVGGWVLLVILALAVGSMTGRVDVSDSEQVPGESGRVSMILDEAGIDEAAGETVLIQAKGGGLTANDPAFREAVDAVIAGVRDTGKVTTPRSPYETKTISADRRSALVQFEMRGDPEKASEHIQPVLDAVDKAQDRHQDLRIEEFGDASGQKAFDDAFGDDFAQAEFSALPVALGILLIVFGALVAALLPVLLAMTAFLATTGLVAVVSHWVHMSDTANSVMLLVGLAVGVDYCLFYLRREREERAAGRDAQTALRVAAATSGRAILVSGVTVIVAMAGMLFTGIAEFKAMGLATLMVVAVAMVGSVTVLPALLSLLGERVEKGRLPFLTRAKRRGGTESRIWRAVLRPVLRRPKLSLALAGGALIALAVPAVGMNTANLTLDQEFGDRLPVVNAYNHIDEAFPGGSDPARVVVKADDIDAPPVRDAIARFRTEAVAKGASKGPVEVTVHREQNLAVVEVPLIGGSDEGKAEKSLDVLRNEVRPATLGAVDGVDAPIGGSTASSKDFNDKLGSAVAPVFAFVVVFAFLLMLMSFRSLTIAVTSIVLNLLSVGAAYGILTAVFQHGWGAGLVGAEGVGAIVSWLPLFLFVILFGLSMDYHVFVVSRIREARLAGRTTKDAVVHGVVTTAGVVTSAAVIMVAVFSIFGTLSMQSMKQMGVGLAAAVLIDATVIRGVLLPATMSLLDERNWYLPKWLRWLPDLAHDEPAPVQRPTTPVGAAPRPDVDERPRHARV
>NZ_CP023992.1|WP_069867133.1|7345431_7346652_+|S8-family-peptidase
MAVHKQRNARRLGLAVAAATAVTAGVFVAVPAGAATTAPAEGTVYGTQAENAVDGSYIVMLKGGKSVKAASEGKDLAEQYGGKLRRTYDSAINGFSASGLTDTEAKRLAADPSVAKVVQNHRYTIKGTQENPPSWGLDRIDQEDTEGDKAYNYPDSAGEGVTAYVIDTGVRTSHKDFEDRATSGFDAVDNDDDADDGNGHGTHVAGTIAGAEHGVAKKAKIVAVRVLDDQGSGTTEQVVAGIDWVTENHEGPSVANMSLGGTPDEALDAAVQKAIDSGVTFGVAAGNESADASGSSPARVEDAITVASSTDQDEQSDFSNYGSVVDIYAPGSDITSDWNTGDDATNTISGTSMATPHVVGAAAVYLSGHQDAKPADVSKALTDGATADKISNPGEDTPNKLLKVVE
>NZ_CP023992.1|WP_099015263.1|7346772_7347369_-|Uma2-family-endonuclease
MTIMSVAETRIDDHEGPWTVEDVLALPEHPARARFELVDGVLMMSPAADWDHQTVSSELHSQIKVALARSGAPFRSGEAVNVMGESRLFIPDIAVVDRAAAPRGTLAAPLEAAVLLGEIVSPFNRAADRILKPALYAQAKVPTYWRVELQPSLHVVVHELDGGTYREAATITGRASVDVAGEFTVDLDLDAVRRELEG
>NZ_CP023992.1|WP_099015264.1|7347538_7349092_-|sporulation-protein
MRNEESSVRRGLGVRMGAVLGAAVVLAVVHPPAQAAPDAGSWTAETVAPGVQLRAGVLRDADAKPSWTVTVQEPGSAPLGDRAWADDTAGRLRGAGFEPRVERVVWAAYADTPHGTMGWRVRLGSYGTSGEAQGAREKVAAAGFTAVAEWTGYDAQQPADRESVHVAVIDPARFTGTVAATHDTSVADRETTSSVAAKRHSLLAVNGGFFITSDADGVQGTMAGIGAYDGELESMAAGSRAALILADGGRHARIADLTSTVTARAGSSTYAVQGINRVPGKVRNCGRPGATPTESPRQDVTCAEADDLVKFTPRFRAALPTGPGTQVVLDADGRVVSTGPRGGTVPAGGSVLQGIGTASDWLTAHARQGERIALNEVVRDTAGRRVRLDSDDSIVSAAPTLVKDGRLAIDAAAEGTLDPKNLSFGYAWSNVRQPRTMAGLDAMGRLILATVDGRQPGVSEGFTLEEAARFMRSLGAVQALNLDGGGSTAMAVNGRLANVTSDATGERAVGDTVQVLP
>NZ_CP023992.1|WP_099015265.1|7349203_7349407_-|DUF397-domain-containing-protein
MEKPMTWRKSSFSGPGETNDCVELATAGGEIRIRESDAPADILTTTPGRLGTFIRAVKAGTLDRLGR

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Crispr_ID: NZ_CP023992_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_17

7509797-7509931

Orphan

Consensus_repeat	Method
CGGCGTCGACAGACGTAAGGCCC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP023992_17

>merge|NZ_CP023992|17|7509797-7509931|CRISPRCasFinder
CGGCGTCGCTGGACTCACGGCTCACGGTCGATGCGGACGGCCTCAAGGCCCACGGACGGCGTCGACAGACGTAAGGCCCACGGACGGCGTCGACAGACGTGAGCTCCGCTGGCGCCGTCGACAGACGTAAGGCCC

>NZ_CP023992|17|17|7509797-7509931|CRISPRCasFinder
CGGCGTCGCTGGACTCACGGCTC	ACGGTCGATGCGGACGGCCTCAAGGCCCACGGA
CGGCGTCGACAGACGTAAGGCCC	ACGGACGGCGTCGACAGACGTGAGCTCCGCTGG
CGCCGTCGACAGACGTAAGGCCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_069867033.1\|7521697_7522522_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|188483
NZ_CP023992.1\|WP_099015326.1\|7505667_7506180_+\|methylated-DNA--[protein]-cysteine-S-methyltransferase	unknown	unknown	gnl\|CDD\|223427
NZ_CP023992.1\|WP_069867040.1\|7513029_7513896_-\|CDP-diacylglycerol--serine-O-phosphatidyltransferase	unknown	unknown	gnl\|CDD\|224104
NZ_CP023992.1\|WP_099017152.1\|7507138_7507765_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099015325.1\|7503874_7505350_+\|DNA-3-methyladenine-glycosylase-2-family-protein	unknown	unknown	gnl\|CDD\|225080
NZ_CP023992.1\|WP_099015327.1\|7506196_7506949_-\|NAD-dependent-deacetylase	unknown	unknown	gnl\|CDD\|238701
NZ_CP023992.1\|WP_099017153.1\|7511331_7512462_+\|glycerate-kinase	unknown	unknown	gnl\|CDD\|376844
NZ_CP023992.1\|WP_099015324.1\|7503192_7503630_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023992.1\|WP_099015329.1\|7508977_7509796_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP023992.1\|WP_099015332.1\|7517401_7519420_-\|protein-meaA	unknown	unknown	gnl\|CDD\|239653
NZ_CP023992.1\|WP_099015333.1\|7519416_7520829_-\|crotonyl-CoA-carboxylase/reductase	unknown	unknown	gnl\|CDD\|188164
NZ_CP023992.1\|WP_099015323.1\|7500965_7503188_-\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP023992.1\|WP_099015328.1\|7507997_7508876_-\|NAD(P)H-binding-protein	unknown	unknown	gnl\|CDD\|187578
NZ_CP023992.1\|WP_159033467.1\|7495225_7499731_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223531
NZ_CP023992.1\|WP_079260733.1\|7514710_7515913_-\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173847
NZ_CP023992.1\|WP_099015330.1\|7509951_7511031_-\|ADP-ribosylglycohydrolase-family-protein	unknown	unknown	gnl\|CDD\|377122
NZ_CP023992.1\|WP_069867037.1\|7515914_7516421_-\|MaoC-family-dehydratase	unknown	unknown	gnl\|CDD\|239535
NZ_CP023992.1\|WP_099015322.1\|7499734_7500865_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|223786
NZ_CP023992.1\|WP_099015331.1\|7516424_7517405_-\|CoA-ester-lyase	unknown	unknown	gnl\|CDD\|225184
NZ_CP023992.1\|WP_079259396.1\|7513882_7514530_-\|phosphatidylserine-decarboxylase	unknown	unknown	gnl\|CDD\|235400

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_069867033.1\|7521697_7522522_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|188483	TIGR03968, transcriptional_regulator_TetR_family, mycofactocin system transcriptional regulator. Members of this family are TetR family putative transcriptional regulators that occur in genome contexts near proteins of the mycofactocin system. These include the precursor peptide (TIGR03969), a radical SAM peptide maturase (TIGR03962), and a putative carrier protein (TIGR03967). [Regulatory functions, DNA interactions].	2.08565e-19
NZ_CP023992.1\|WP_099015326.1\|7505667_7506180_+\|methylated-DNA--[protein]-cysteine-S-methyltransferase	gnl\|CDD\|223427	COG0350, Ada, Methylated DNA-protein cysteine methyltransferase [DNA replication, recombination, and repair].	1.55853e-58
NZ_CP023992.1\|WP_069867040.1\|7513029_7513896_-\|CDP-diacylglycerol--serine-O-phosphatidyltransferase	gnl\|CDD\|224104	COG1183, PssA, Phosphatidylserine synthase [Lipid metabolism].	1.00065e-32
NZ_CP023992.1\|WP_099015325.1\|7503874_7505350_+\|DNA-3-methyladenine-glycosylase-2-family-protein	gnl\|CDD\|225080	COG2169, Ada, Adenosine deaminase [Nucleotide transport and metabolism].	1.84422e-58
NZ_CP023992.1\|WP_099015327.1\|7506196_7506949_-\|NAD-dependent-deacetylase	gnl\|CDD\|238701	cd01410, SIRT7, SIRT7: Eukaryotic and prokaryotic group (class4) which includes human sirtuin SIRT6, SIRT7, and several bacterial homologs; and are members of the SIR2 family of proteins, silent information regulator 2 (Sir2) enzymes which catalyze NAD+-dependent protein/histone deacetylation. Sir2 proteins have been shown to regulate gene silencing, DNA repair, metabolic enzymes, and life span.	9.33162e-88
NZ_CP023992.1\|WP_099017153.1\|7511331_7512462_+\|glycerate-kinase	gnl\|CDD\|376844	pfam02595, Gly_kinase, Glycerate kinase family. This is family of Glycerate kinases.	1.49149e-163
NZ_CP023992.1\|WP_069867037.1\|7515914_7516421_-\|MaoC-family-dehydratase	gnl\|CDD\|239535	cd03451, FkbR2, FkbR2 is a Streptomyces hygroscopicus protein with a hot dog fold that belongs to a conserved family of proteins found in prokaryotes and archaea but not in eukaryotes. FkbR2 has sequence similarity to (R)-specific enoyl-CoA hydratase, the peroxisomal Hydratase-Dehydrogenase-Epimerase (HDE) protein, and the fatty acid synthase beta subunit. The function of FkbR2 is unknown.	1.32887e-70
NZ_CP023992.1\|WP_099015329.1\|7508977_7509796_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.07508e-12
NZ_CP023992.1\|WP_099015332.1\|7517401_7519420_-\|protein-meaA	gnl\|CDD\|239653	cd03681, MM_CoA_mutase_MeaA, Coenzyme B12-dependent-methylmalonyl coenzyme A (CoA) mutase (MCM) family, MeaA-like subfamily; contains various methylmalonyl coenzyme A (CoA) mutase (MCM)-like proteins similar to the Streptomyces cinnamonensis MeaA, Methylobacterium extorquens MeaA and Streptomyces collinus B12-dependent mutase. Members of this subfamily contain an N-terminal MCM domain and a C-terminal coenzyme B12 binding domain. S. cinnamonensis MeaA is a putative B12-dependent mutase which provides methylmalonyl-CoA precursors for the biosynthesis of the monensin polyketide via an unknown pathway. S. collinus B12-dependent mutase may be involved in a pathway for acetate assimilation.	0
NZ_CP023992.1\|WP_099015333.1\|7519416_7520829_-\|crotonyl-CoA-carboxylase/reductase	gnl\|CDD\|188164	TIGR01751, crotonyl_CoA_reductase, crotonyl-CoA carboxylase/reductase. The enzyme represented by this model can convert crotonyl-CoA to butyryl-CoA (crotonyl-CoA reductase activity), but more importantly, in the presence of CO2, generates (2S)-ethylmalonyl-CoA. In serine cycle methylotrophic bacteria this enzyme is involved in the process of acetyl-CoA to glyoxylate. In other bacteria the enzyme is used to produce extender units for incorporation into polyketides such as tylosin from Streptomyces fradiae and coronatine from Pseudomonas syringae.	0
NZ_CP023992.1\|WP_099015323.1\|7500965_7503188_-\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	1.0899e-05
NZ_CP023992.1\|WP_099015328.1\|7507997_7508876_-\|NAD(P)H-binding-protein	gnl\|CDD\|187578	cd05269, TMR_SDR_a, triphenylmethane reductase (TMR)-like proteins, NMRa-like, atypical (a) SDRs. TMR is an atypical NADP-binding protein of the SDR family. It lacks the active site residues of the SDRs but has a glycine rich NAD(P)-binding motif that matches the extended SDRs. Proteins in this subgroup however, are more similar in length to the classical SDRs. TMR was identified as a reducer of triphenylmethane dyes, important environmental pollutants. This subgroup also includes Escherichia coli NADPH-dependent quinine oxidoreductase (QOR2), which catalyzes two-electron reduction of quinone; but is unlikely to play a major role in protecting against quinone cytotoxicity. Atypical SDRs are distinct from classical 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.	2.06343e-73
NZ_CP023992.1\|WP_159033467.1\|7495225_7499731_-\|hypothetical-protein	gnl\|CDD\|223531	COG0455, flhG, Antiactivator of flagellar biosynthesis FleN, an ATPase [Cell motility].	2.88035e-24
NZ_CP023992.1\|WP_079260733.1\|7514710_7515913_-\|acyl-CoA-dehydrogenase	gnl\|CDD\|173847	cd01158, SCAD_SBCAD, Short chain acyl-CoA dehydrogenases and eukaryotic short/branched chain acyl-CoA dehydrogenases. Short chain acyl-CoA dehydrogenase (SCAD). SCAD is a mitochondrial beta-oxidation enzyme. It catalyzes the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of SCAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. This subgroup also contains the eukaryotic short/branched chain acyl-CoA dehydrogenase(SBCAD), the bacterial butyryl-CoA dehydorgenase(BCAD) and 2-methylbutyryl-CoA dehydrogenase, which is involved in isoleucine catabolism. These enzymes are homotetramers.	7.9187e-135
NZ_CP023992.1\|WP_099015330.1\|7509951_7511031_-\|ADP-ribosylglycohydrolase-family-protein	gnl\|CDD\|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	3.83356e-40
NZ_CP023992.1\|WP_099015322.1\|7499734_7500865_-\|AAA-domain-containing-protein	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.41838e-16
NZ_CP023992.1\|WP_099015331.1\|7516424_7517405_-\|CoA-ester-lyase	gnl\|CDD\|225184	COG2301, CitE, Citrate lyase beta subunit [Carbohydrate transport and metabolism].	1.57848e-75
NZ_CP023992.1\|WP_079259396.1\|7513882_7514530_-\|phosphatidylserine-decarboxylase	gnl\|CDD\|235400	PRK05305, PRK05305, phosphatidylserine decarboxylase family protein.	1.81184e-91

>NZ_CP023992.1|WP_099015329.1|7508977_7509796_+|TetR/AcrR-family-transcriptional-regulator
MESEDVTAADGTHTVNREGSHEAKPDGSHDTPSDGNRDRDGNGTRDGNRERIVAAAARLLSDGGPDAVSTRAVSSAAGVQPPTIYRLFGDKQGLLDAVVAYGFTEYLSSKAAHEAGDDPVEDLRAGWDLHIGLGLANPALYSLMYGGHRPGVPSPAAVAAFDMLARLIRRIAEAGRLAIPEERAAALVHAAGCGTTLTLIATPEARRDPELSRTAREAAIAAITTDAPAAAEPGPVAAAVTLRAALPRTDALTVPERNLLREWLDRIADPAR
>NZ_CP023992.1|WP_099015328.1|7507997_7508876_-|NAD(P)H-binding-protein
MIIVTGANGQLGRMVTERLLERVPAREIGVSVRDVDATQDLGAKGVRVRMGDFTGPATLAHAFEGASKVLIVSTDSTGETAVRHHRTAVEAAAKAGAQRILYTSHMGSNPSSPFPPMPDHAATEEALRQSGVPFTSLRNGFYASSAVMLISAALETGVLAAPEDGPVAWTAHTDLADAAVLALTGETLTDAAPDGLTPALTGPEAIDMAGIADILTRLTGRPIRRVVVSDADYRARLLSAGLPEHAADMLVGLFAASRDGDFAPADPTLADLLGRPTVRMEDYLKSALAPAR
>NZ_CP023992.1|WP_099017152.1|7507138_7507765_+|hypothetical-protein
MRISDDPARRGRTSRPLAFPERRNPSGGGLPEYRAARKEGTRAFTLWADPHRGQVFAQVATKSATKGGPATYEVLGAAGEPLALVTRRPAMKGGLRTRWTVQQTGSRPAVGCKGRPVWWGVWWLFLPLQLLIVIGSVLNGGGDPARTPRRTRWRLDRRVVLDFHSGPGTAFELKVVTDGWDDRVTAALVALLDSHGGWLGSAWDTAEH
>NZ_CP023992.1|WP_099015327.1|7506196_7506949_-|NAD-dependent-deacetylase
MSSETTHRPLVAILSGAGISTDSGIPDYRGPQGLWRRDPEAEKLVTYEYYMTDPEIRRRSWLMRRDSETLRARPNGAHEAVARLERSGVPVRVITQNVDGLHQIAGMPARKVLELHGTARAVRCTHCQARSGMAEALERVAAGEADPACRECGGILKSATVMFGESLDPDVLTEAVAVARACDIFIAVGTSLQVQPAASLAGLAAEHGARLIIVNAEPTPYDGLADEVVREPISVALPAVLDRIAVGDGG
>NZ_CP023992.1|WP_099015326.1|7505667_7506180_+|methylated-DNA--[protein]-cysteine-S-methyltransferase
MTRTHTTIDSPYGPLTLVATGTELSGLYMVQQRHRPPEETFGAPGDPADTPFAETIRQLTAYFAGELTEFDLPLHLDGTPFQRRVWAELRRIPYGETWSYGRLADRIGQPTASRAVGLANGKNPVGIIVPCHRVVGSSGSLTGYGGGLDRKRRLLEFEARQERQELPGLF
>NZ_CP023992.1|WP_099015325.1|7503874_7505350_+|DNA-3-methyladenine-glycosylase-2-family-protein
MHTDTDRCLRAAQAKDARFDGWFFIAVVTTGIYCRPSCPVVGPKPENMRFYPSAAAAQQAGFRACKRCRPDASPGSPQWNERADLVARAMRLIADGVVDRDGVPGLAARLGYSTRQVERQLLAELGAGPLALARAQRAQTARLLIETSELPMADIAFAAGFASVRAFNETVREIFALAPTELRQRARRGPRASVPGALTLRLPFRAPLCPDNLFGHLAATAVPGVEEWRDGAYRRTLRLPYGPGVVTLRPRPDHIACQLSLADLRDLAGAISRCRRLLDLDADPAAVDDLLRTDLQLAPLVDKAPGRRVPRAVDADEFAVRAVLGQQVSTAAARTHAGRLVVAHGEPVEDPAGGLTHLFPSAQALAGLDPEKLAMPRTRRTTLTGLVGALAGGRVALGVGSDWDDARASLGALPGLGPWTVEVIAMRALGDPDAFLPTDLGVRRAAAELGLPATPGALTRHSARWRPWRAYAVQYLWATDPAHAINRIPAA
>NZ_CP023992.1|WP_099015324.1|7503192_7503630_-|hypothetical-protein
MIGMMRNVTEHREIPLANGTTVRLELAPVGEPSPEDAYGGVGGVTPVGRGARAAATLANAGLGVILEGLGSVLQEVHDAVRSTPHPPEEFTVQFGVQVGQDLKLGIVGANGNANLTISATWRPSEESGPTVPTVPPRPSHSGPTA
>NZ_CP023992.1|WP_099015323.1|7500965_7503188_-|trypsin-like-peptidase-domain-containing-protein
MGWFHAHGSSSRPAVSILAKADGRPAGAGVLLPRRHLLTCAHVVNSALGKDMLAPDHPGPIAVSVRLHAPEHTVEADAELAVWIPPRTDDGGLGAFEWNGDLAVLRLTGALPPAVEPPRWHPMAERQLVRAWHGSGEPGVFADAEVSECDGRFGYFDGAERTLDIEPAYSGGPLWSNEESAVVGLVTAKLRVRGTLRRAWGIPWQRVTRELDDAGAGHLLPRQPAEDIRDHPAYGELVALLDGPLALSEGWTRCCRTVARQCGLGHRADGLPSADEFAHLLLTRARALPALVEAVRGTAGPVADDILAIGRRHGLPKLLSPGEHERLLVQLRALPATAAAGVPGAVRAALPLAALPTALLTGEDGGHGCDGGVGGHGRHDVNGGQRDERFEALIAHLEGLHGDSSPADDGAMTVPGLLRAVEFVAAGCCPADQGAALRRWNAAVARRLGVHDAALMDRRHDAGQWARSASRGAAPRVVAKLDPCGPASGGGTTTTATAAREEPERYRLRLWCDDGDGLRQVSDDSERPRGAEEVAQEIFAAVGSLRRPDPSGPRPVIELIVDRDALEVPVDRWKAAGPGAVLPIRLGTPYPLVVNCPELRELNGGTMLDQWRERWTRLDAEEPLHIDDATAPDPEAVCGLVMERLTARVTIDVAPHRRTGVVQMCLAAGVPVVLWDRSGEPESPAVRHAAGMSARELPEAVRIYRTKTMQRPEEYTGRPVLAWADAGRALPRLDLADPTE
>NZ_CP023992.1|WP_099015322.1|7499734_7500865_-|AAA-domain-containing-protein
MSAEAGREGGSPMNPPERDDWRLFRGDGVPRHMEMPPAPPWRRFGGGERPSPEGERLSPEGERPSPEEERPSPEGERAAPGEERAVPGEEQAPPASGRSRPAPYLIAPEHADVVNAALHLRRPLLVTGSPGTGKSSLARAIAHELDLGEVLRWPVNSRSTVQDALYRYDAIGRLRETALRRDRDEAEPDIGSFVRLGPLGTALVPGERPRALLVDELDKGDVDLPNDLLTVFEEGEFEIPELARLPEDQSVVEVLTERPGERATVRRGRLVCDEFPVVVITSNGERDFPPAFLRRCVRLELPTPDEGRLRAIVTAHLGDDALEEVDQLLDTFLRRRAARELATDQLLNAVFLRAGGMDVTAEGLLEAVLHRLGGAV
>NZ_CP023992.1|WP_159033467.1|7495225_7499731_-|hypothetical-protein
MAGGGTGRLARLDEAMAILTAGGLELSREELLDALWLAGRLPEDGPERAPLARAVTRGGTALPATRPEPARPAATASPAASVQQTAQHTAQPTAQPTGPARTPRANGSVPGAQPSSPAQRQPDVPQDQRHGLTPPRDDRQLRGLYGGSQGAGEGGADGAEDAAADARRALPLRVPEDKALHQELSIGRALRPLKQHRPNPLRREFDEAATATALAETGLPDVVTRPARERWLDLALVIDDGMSMLLWRRLAVELRTVLQRSGAFRVVRVLGLRTRGGDAPALRARPYAPDAPLLPTTALSDPSGHTLVLVVSDGVGAAWRDGRMGQVLARWAGVGPTAVVHALPPRLWEGSGIRARRWQVRTRRPGSANTDWTVADPVLPAALARFEGVPVPVLEPDAGPLADWARLIASASGTAVLPLLDPGRGGPRPAPAAAPGPADEVGRVQRFRDAASPEAYRLAAHMAAVAPLPVPVMRMVQKAVDGRTDTGRLAEVFLGGLMLPVEPPASAGQDPLPPEHRPFTFTDAAQRALLGAVPLAELVSTSRLIGRRLEQLAGRSPDFPAWLADPGGSDRLPAGARPFSAVERRLAARLGAPPRPSVFTTPTATRTWRHLEPGDPRTLGPYRLTMAGPPGARLTPYLGQDAYDAEAVLQTARHARGEAAAALLDVQAEALRRMDGRYARRLLREGLTDDVPWIAEEAFIGERLDYVLRGHAEQWGDRPDDALLAAPERWDGHTALALARKVADAVRTSEDAGVVHGDLSVSTVHIAGEDILLTGWSSAAIDGTPSPASAGGRPPAPEDNVKALGDILLCLGGGALARRPAPGLYFMPRWSSAVWEPLRAVVMACRENPRRHTAYGIWELLMEFRPDAAPPRARAEQPSPRVRRPLFRPGGPLACSRCGNPLEPDDRFCDGCGVDLYSSPPVSAPPRPEPGSARAPRAEPGSALPSVDGYRAYRRLGGSQGRDVYLARRPGAQREVVIRMAPGAGRELRAEAEALRRMSGHYAPRLFVDASSSNPPWLVMECVRLPDGSPAPPLSSLLGREPDGSSKLDPVHAATIGLRLAEAVNMCALKGIVPGTLTPDTVLVTDRTVKLIGWTDANLNDRLPGAPTPADSVYALGKILRALSDSQPTARLSQAGALWQNPLSIISACLNEQPSKRPSASQVADVFVKSLPTVRASAHTPYEAETPAATPPPDGTPEAEPAPTMAAEPPPSRSTRSRLAALVGLGGRSAKAEQRQHKLDLIRTPLPSCHRIAVISRPVSAGRTVTTLALGAVLAGERQDEVIAVDAMPGGDTLSRRVDARSDWTVHDLARADLPGDDADSIRRFTSRLPSGLEVLLGDPTPMSLVGRAAPIDDMEYRRVMALLARHYPIVLSDSDTGALRDSMRGILDLADQLIIVTTPSVEYMRSAHITLDQLAEDGHADLVRRVITVVNMSHDVPWTDHYEGLTAGFRDRSRGVVVVPYDEHLASRGEIDLRRLASRTLDAYLDLAALVAEGFPGAGD
>NZ_CP023992.1|WP_099015330.1|7509951_7511031_-|ADP-ribosylglycohydrolase-family-protein
MTLSGSALADRIHGGWLGRIAGNMLGKPVENGEHWTRDRIDRYLRRADALPLTDYLPALEPPPDPVEFELRPEWQRCVRGRIHGSCRDDDVDYSVLGLHLLETHGPGFSTEQVGEMWLLRLPYLQTFTAERAAYRNLTAGVKPPLSATLDNPYQEWIGALIRADIHGWVNPGDPHRAAAMARRDAVLSHTGNGVYGAMWAAALVAAAFTADGPRAAVASALDRIPPRCRLARTVRRAMSLYDAGVAWADALAQLEKETAGLHWIHVVPNAAVLTAGLLYGAGDFTATIALTVRGGLDTDSNGATAGSVAGVLCGAAAIPPQWTEPLEDRVRSAVFGFDGARISDLAARTHRLAVSSAER
>NZ_CP023992.1|WP_099017153.1|7511331_7512462_+|glycerate-kinase
MIAADKFKGSLTAVEVAERVTAGLRRGAPHGGEGLRIEALPVADGGDGTVDAAVAAGFERREVRVTGPLGAPVTAAYALHGATAVVEMAEASGLRHLPAGVFAPLTATTYGSGELLRAALDAGARTIVFGVGGSATTDGGAGMLSALGARFLRADGTPVAPGGGPLRDLATADLSGLDPRLADTETVLASDVDNPLTGPKGAAAVYGPQKGAGEDDVAALDTALAHYVRVLERAVGAPAAEYALAPGAGAAGGIGFGALVGLGATFRPGIEVMLDVLGFPAALEGADLVITGEGSLDEQTLHGKAPAGVAAAARARGIEVVAVCGRLALAPAALGNAGIRRAYALTDLEPDPARCIAEAGPLLERTAERLAKDFLP
>NZ_CP023992.1|WP_069867040.1|7513029_7513896_-|CDP-diacylglycerol--serine-O-phosphatidyltransferase
MTVIDPDTQAAWVPEAEVDEADVDETDDMPLSTRLSIADTLTLGNATCGFLAVYFTTTGVLIPHLTGSEDGGMTRHSAASAVMLMLLASVFDLFDGLVARKLRSSAMGAELDNLSDLISFGLAPAYFVLVWGMVSDDAYQRVSVVGAIVVLLAVVLRLARFSCVTLRDGVFQGMPSPFGALTVVSVVLLGLPFVPTLLAIIGVAWLMVSRVEYPKPRGRLAVAMLSWIVTSMALLAAWAFEAPGGELLLQSACALQVVMGAVIPLFATARRVNAFRDNRREARAAQLP
>NZ_CP023992.1|WP_079259396.1|7513882_7514530_-|phosphatidylserine-decarboxylase
MPHSQSSAQRGRVRLARGASPWLLPTVATAAVSLARARRSGRWTAVAVPATALAAGMLWFFRDPEREITQGRVISPADGVVQSIMPWKDGRTRVAIFMSPLNVHVNRAPLAGTVTSVEHIPGGFVPAFNKESENNERVVWHFDTELGDIEMVQIAGAVARRIVPYVPQGTKVEQGERIGLIRFGSRVDIYLPEGVDVAVEVGQATTAGVTRLDRD
>NZ_CP023992.1|WP_079260733.1|7514710_7515913_-|acyl-CoA-dehydrogenase
MSRLAQTEGLTDIQREILSTVRDFVDKEILPVATELEHRDEYPTAIVEGLKELGVFGLMIPEEYGGLGESLLTYALCVEEIARGWMSVSGIINTHFIVAYMLKQHGTEEQKEYFLPKMALGEIRGAFSMSEPGLGSDVSAITSKAVPDGDEYVLNGQKMWLTNGGTATLVAVLCRTGEAQEGVAPHKAMTTFLVEKEPGFGEVRPGLTIPGKIEKMGYKGVDTTELIMDGLRIPADRVLGGTPNRGFYQMMDGVEVGRVNVAARGCGVARRAFELGVAYAQQRHTFGKPIAQHQAIQFKLAEMGTKVEAAHAMMVNAARKKDSGARNDLEAGMAKYLASEYCKEVVEDAFRIHGGYGFSKEYEIERLYREAPMLLIGEGTAEIQKMIIGRRLLEEYRTQD
>NZ_CP023992.1|WP_069867037.1|7515914_7516421_-|MaoC-family-dehydratase
MQFGRTYEEFTVGDVYRHWPGKTVTEYDDHLFCLLTMNHHPLHMDSNYAEKTTDFGKNVVVGNYIYSLLLGMSVPDVSGKAIANLEIESLRHVAPTFHGDTIYGETTVLGKTPSKSKTDRGIVHVETKGYKQDGTLVCVFRRKVMVPTATYIKERGGEQPGRPELGGQ
>NZ_CP023992.1|WP_099015331.1|7516424_7517405_-|CoA-ester-lyase
MTAPDRSDAASRLRPRRSCLAVPGSNPRFLEKAQGLPADQVFLDLEDACAPLAKEDARHTIVKALNEGDWTGKTRVVRVNDWTTHWTYRDVITVVEGAGPNLDCIMLPKVQDAQQIIALDLLLTQIEKTMGFETGRIGIEAQIENAKGLVNVDEIAGASPRLETIVFGPADFMASINMKSLVVGEQPPGYPADAYHYILMRILMAARTHDLQAIDGPYLQIRNVDGFREVAGRAAALGYDGKWVLHPGQVEAANEVFSPSQEDYDHAELILDAYDYCTSAEGGMKGSAMLGDEMIDEASRKMALVIAGKGRAAGMARTSTFQPPEA
>NZ_CP023992.1|WP_099015332.1|7517401_7519420_-|protein-meaA
MSGAPRPKDRPWLMRTYAGHSTAEASNELYRRNLAKGQTGLSVAFDLPTQTGYDPDHILARGEVGRVGVPVSHLGDMRRLFQEIPLERMNTSMTINATAMWLLALYQVVAEEHGADIAKLQGTTQNDIVKEYLSRGTHVFPPGPSLRLTTDMIAYTVHHVPKWNPINICSYHLQEAGATPVQEIAFAMSTAIAVLDAVFASGQVPEDRKGDVVARISFFVNAGVRFIEEMCKMRAFGRIWDRITRERYGIENAKHRRFRYGVQVNSLGLTEAQPENNIQRIVLEMLAVTLSKDARARAVQLPAWNEALGLPRPWDQQWSLRIQQVLAHESDLLEYDDIFEGSKVIESKVAALVEEADAEIERIQEMGGAMAAVESGYLKARLVASHSERRARIEAGEEKIVGVNCYESTEPTPLTADLDTAIMTVDPENEARVVSALHSWREQRDEGPAQEALAALRKAAAGTENLMEATLRCARAGVTTGEWAWALRDVFGEYRAPTGVGGAPLTVATETGSPLASVREKVDKTVAELGGGRLRLLVGKPGLDGHSNGAEQIAVRARDAGFEVVYQGIRLTPEQIVSAAVAEDVHCVGLSILSGSHAELVPDVLDRLRAAGAQDIPVIVGGIIPAADAAALRAAGVAAVFTPKDFGITEIIGRIVDEIRAANTLPPLEVLV
>NZ_CP023992.1|WP_099015333.1|7519416_7520829_-|crotonyl-CoA-carboxylase/reductase
MNEILDAILASDTAPEDFAALPIPESYRAVTVRKDEAEMFSGLTTREKDPRKSLHVDEVPVPELGPGEALVAVMASSVNYNSVWTSIFEPLPTFGFLERYGKLSPLAKRHDLPYHIIGSDLAGVVLRTGPGVNVWQPGAEVVAHCLSVELESADGHNDTMLDPEQRIWGFETNFGGLAEIALVKSNQLMPKPAHLSWEEAAAPGLVNSTAYRQLVSRNGAGMKQGDNILIWGASGGLGSYATQYALAGGATPVCVVSSPRKAEICRRMGAEAIIDRTAEDYTFWKDDGTQDPREWKRLGKKIRELTGGEDVDIVFEHPGRETFGASVYVTRKGGTIVTCASTSGYTHEYDNRYLWMSLKRIVGSHFANYREAWEANRLIAKGKIHPTLSRTYRLEDTGQAAYDVHRNRHQGKVGVLCLAPEEGMGVRDQAMRDQHIDAINLFRDDLSERTNKRSRDDLSERTNKRSEDVR
>NZ_CP023992.1|WP_069867033.1|7521697_7522522_-|TetR-family-transcriptional-regulator
MSQPVKATRTERTKRSPSSGAGGSAGSRRAAAQRLSMRRKLAAAAMELFATQGYEATTVDEIAARAGVARRTFFRHFRSKEEAIFPDHDDTLVRAAEVLDAAPPHENPLDTVCRGIKEVMRMYASAPSVSVERYQLTREVPALREREIASVARYERLFTRYLLGHFDEGAHHDGDDDPLLAEVAASAVVTAHNHVLRRWLRAGGEGDVETQLDHAFAIVRETFGNGIGGRPTVAGGRPAATVSATKEDEVMVMVARTDAPLTEVMRTIREALKR

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Crispr_ID: NZ_CP023992_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023992_18

8038971-8039088

Orphan

Consensus_repeat	Method
CTGCCGGTGGGCGGGTGCGGCGCCGTCGTGGCTGGGCGCGC	CRISPRCasFinder

1 spacers

csa3

The CRISPR arrays of NZ_CP023992_18

>merge|NZ_CP023992|18|8038971-8039088|CRISPRCasFinder
CTGCCGGTGGGCGGGTGCGGCGCCGTCGTGGCTGGGCGCGCCCCTGCGGCGGAGCCGTACGGGGCGTCTGCCCCTATCTGCCGGTGGGCGGGTGCGGCGCCGTTGTGGCTGGGCGCGC

>NZ_CP023992|18|18|8038971-8039088|CRISPRCasFinder
CTGCCGGTGGGCGGGTGCGGCGCCGTCGTGGCTGGGCGCGC	CCCTGCGGCGGAGCCGTACGGGGCGTCTGCCCCTAT
CTGCCGGTGGGCGGGTGCGGCGCCGTTGTGGCTGGGCGCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023992.1\|WP_093702616.1\|8044673_8046056_-\|nitrate-reductase	unknown	unknown	gnl\|CDD\|132655
NZ_CP023992.1\|WP_069869821.1\|8043761_8044628_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|375319
NZ_CP023992.1\|WP_099015564.1\|8030309_8030894_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|188483
NZ_CP023992.1\|WP_099015572.1\|8049827_8051132_+\|alginate-lyase-family-protein	unknown	unknown	gnl\|CDD\|377511
NZ_CP023992.1\|WP_099015565.1\|8031020_8032223_+\|FAD-dependent-monooxygenase	unknown	unknown	gnl\|CDD\|223727
NZ_CP023992.1\|WP_167460047.1\|8041953_8042649_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235215
NZ_CP023992.1\|WP_167459959.1\|8032367_8033849_-\|integrin-like-protein	unknown	unknown	gnl\|CDD\|379232
NZ_CP023992.1\|WP_069869815.1\|8036988_8038461_+\|amino-acid-permease	unknown	unknown	gnl\|CDD\|129987
NZ_CP023992.1\|WP_099015569.1\|8042744_8043629_-\|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223528
NZ_CP023992.1\|WP_099017184.1\|8048473_8049700_+\|ROK-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224851
NZ_CP023992.1\|WP_069869817.1\|8039320_8040118_+\|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|143600
NZ_CP023992.1\|WP_099015570.1\|8046124_8047009_-\|isocitrate-lyase/phosphoenolpyruvate-mutase-family-protein	unknown	unknown	gnl\|CDD\|379346
NZ_CP023992.1\|WP_093705313.1\|8035731_8036487_-\|DUF2637-domain-containing-protein	unknown	unknown	gnl\|CDD\|378511
NZ_CP023992.1\|WP_099015562.1\|8029265_8029802_-\|ATPase	unknown	unknown	gnl\|CDD\|176903
NZ_CP023992.1\|WP_099015566.1\|8034159_8035623_+\|GuaB1-family-IMP-dehydrogenase-related-protein	unknown	unknown	gnl\|CDD\|181127
NZ_CP023992.1\|WP_099015568.1\|8040185_8041895_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|366721
NZ_CP023992.1\|WP_099015567.1\|8038471_8038927_+\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224439
NZ_CP023992.1\|WP_099015563.1\|8029785_8030148_-\|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|238042
NZ_CP023992.1\|WP_099015571.1\|8047095_8048328_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340951
NZ_CP023992.1\|WP_069869814.1\|8036483_8036690_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023992.1\|WP_093702616.1\|8044673_8046056_-\|nitrate-reductase	gnl\|CDD\|132655	TIGR03616, Putative_pyrimidine_permease_RutG, pyrimidine utilization transport protein G. This protein is observed in operons extremely similar to that characterized in E. coli K-12 responsible for the import and catabolism of pyrimidines, primarily uracil. This protein is a member of the uracil-xanthine permease family defined by TIGR00801. As well as the The Nucleobase:Cation Symporter-2 (NCS2) Family (TC 2.A.40).	3.78843e-104
NZ_CP023992.1\|WP_069869821.1\|8043761_8044628_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|375319	pfam17765, MLTR_LBD, MmyB-like transcription regulator ligand binding domain. This domain is found in a family of actinobacterial transcription factors. The structure shows it has a PAS domain like fold and it is bound to Myristic acid.	7.41488e-47
NZ_CP023992.1\|WP_099015564.1\|8030309_8030894_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|188483	TIGR03968, transcriptional_regulator_TetR_family, mycofactocin system transcriptional regulator. Members of this family are TetR family putative transcriptional regulators that occur in genome contexts near proteins of the mycofactocin system. These include the precursor peptide (TIGR03969), a radical SAM peptide maturase (TIGR03962), and a putative carrier protein (TIGR03967). [Regulatory functions, DNA interactions].	3.09285e-20
NZ_CP023992.1\|WP_099015572.1\|8049827_8051132_+\|alginate-lyase-family-protein	gnl\|CDD\|377511	pfam05426, Alginate_lyase, Alginate lyase. This family contains several bacterial alginate lyase proteins. Alginate is a family of 1-4-linked copolymers of beta -D-mannuronic acid (M) and alpha -L-guluronic acid (G). It is produced by brown algae and by some bacteria belonging to the genera Azotobacter and Pseudomonas. Alginate lyases catalyze the depolymerization of alginates by beta -elimination, generating a molecule containing 4-deoxy-L-erythro-hex-4-enepyranosyluronate at the nonreducing end. This family adopts an all alpha fold.	2.58429e-96
NZ_CP023992.1\|WP_099015565.1\|8031020_8032223_+\|FAD-dependent-monooxygenase	gnl\|CDD\|223727	COG0654, UbiH, 2-polyprenyl-6-methoxyphenol hydroxylase and related FAD-dependent oxidoreductases [Coenzyme metabolism / Energy production and conversion].	1.82661e-30
NZ_CP023992.1\|WP_167460047.1\|8041953_8042649_-\|hypothetical-protein	gnl\|CDD\|235215	PRK04053, rps13p, 30S ribosomal protein S13P; Reviewed.	0.00832782
NZ_CP023992.1\|WP_167459959.1\|8032367_8033849_-\|integrin-like-protein	gnl\|CDD\|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	2.19737e-05
NZ_CP023992.1\|WP_069869815.1\|8036988_8038461_+\|amino-acid-permease	gnl\|CDD\|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	4.27854e-176
NZ_CP023992.1\|WP_099015569.1\|8042744_8043629_-\|NAD(P)-dependent-oxidoreductase	gnl\|CDD\|223528	COG0451, WcaG, Nucleoside-diphosphate-sugar epimerases [Cell envelope biogenesis, outer membrane / Carbohydrate transport and metabolism].	3.49628e-31
NZ_CP023992.1\|WP_099017184.1\|8048473_8049700_+\|ROK-family-transcriptional-regulator	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	2.64066e-34
NZ_CP023992.1\|WP_069869817.1\|8039320_8040118_+\|carbon-nitrogen-hydrolase-family-protein	gnl\|CDD\|143600	cd07576, R-amidase_like, Pseudomonas sp. MCI3434 R-amidase and related proteins (putative class 13 nitrilases). Pseudomonas sp. MCI3434 R-amidase hydrolyzes (R,S)-piperazine-2-tert-butylcarboxamide to form (R)-piperazine-2-carboxylic acid. It does so with strict R-stereoselectively. Its preferred substrates are carboxamide compounds which have the amino or imino group connected to their beta- or gamma-carbon. This subgroup belongs to a larger nitrilase superfamily comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), class 13 represents proteins that at the time were difficult to place in a distinct similarity group. It has been suggested that this subgroup represents a new class. Members of the nitrilase superfamily generally form homomeric complexes, the basic building block of which is a homodimer. Native R-amidase however appears to be a monomer.	5.57136e-125
NZ_CP023992.1\|WP_099015570.1\|8046124_8047009_-\|isocitrate-lyase/phosphoenolpyruvate-mutase-family-protein	gnl\|CDD\|379346	pfam13714, PEP_mutase, Phosphoenolpyruvate phosphomutase. This domain includes the enzyme Phosphoenolpyruvate phosphomutase (EC:5.4.2.9). This protein has been characterized as catalyzing the formation of a carbon-phosphorus bond by converting phosphoenolpyruvate (PEP) to phosphonopyruvate (P-Pyr). This enzyme has a TIM barrel fold.	3.50091e-67
NZ_CP023992.1\|WP_093705313.1\|8035731_8036487_-\|DUF2637-domain-containing-protein	gnl\|CDD\|378511	pfam10935, DUF2637, Protein of unknown function (DUF2637). This family of proteins has no known function.	0.000685837
NZ_CP023992.1\|WP_099015562.1\|8029265_8029802_-\|ATPase	gnl\|CDD\|176903	cd08894, SRPBCC_CalC_Aha1-like_1, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	1.79373e-66
NZ_CP023992.1\|WP_099015566.1\|8034159_8035623_+\|GuaB1-family-IMP-dehydrogenase-related-protein	gnl\|CDD\|181127	PRK07807, PRK07807, GuaB1 family IMP dehydrogenase-related protein.	0
NZ_CP023992.1\|WP_099015568.1\|8040185_8041895_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|366721	pfam01593, Amino_oxidase, Flavin containing amine oxidoreductase. This family consists of various amine oxidases, including maze polyamine oxidase (PAO) and various flavin containing monoamine oxidases (MAO). The aligned region includes the flavin binding site of these enzymes. The family also contains phytoene dehydrogenases and related enzymes. In vertebrates MAO plays an important role regulating the intracellular levels of amines via there oxidation; these include various neurotransmitters, neurotoxins and trace amines. In lower eukaryotes such as aspergillus and in bacteria the main role of amine oxidases is to provide a source of ammonium. PAOs in plants, bacteria and protozoa oxidase spermidine and spermine to an aminobutyral, diaminopropane and hydrogen peroxide and are involved in the catabolism of polyamines. Other members of this family include tryptophan 2-monooxygenase, putrescine oxidase, corticosteroid binding proteins and antibacterial glycoproteins.	4.12061e-48
NZ_CP023992.1\|WP_099015567.1\|8038471_8038927_+\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	1.88887e-30
NZ_CP023992.1\|WP_099015563.1\|8029785_8030148_-\|winged-helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	2.26078e-19
NZ_CP023992.1\|WP_099015571.1\|8047095_8048328_-\|MFS-transporter	gnl\|CDD\|340951	cd17393, MFS_MosC_like, Membrane protein MosC and similar proteins of the Major Facilitator Superfamily of transporters. The gene encoding Sinorhizobium meliloti membrane protein MosC is part of the mos locus, which encodes the biosynthesis of the rhizopine 3-O-methyl-scyllo-inosamine. MosC belongs to the bacterial fucose permease, eukaryotic Major facilitator superfamily domain-containing protein 4 (FucP/MFSD4) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.83963e-90

>NZ_CP023992.1|WP_099015567.1|8038471_8038927_+|Lrp/AsnC-family-transcriptional-regulator
MRLNDLDERIVHALAEDARRSYADIGELVGLSAPAVKRRVDRLRAEGAITGFTVRVDPIALGWETEGFIELFCRHNTSPGDIRRGLSRYPEVVSASTVTGDADAVVQVFASDMRHFERVLERIAGEPFVERTKSVLVLSPLLRRFGAGAPT
>NZ_CP023992.1|WP_069869815.1|8036988_8038461_+|amino-acid-permease
MLEHGAAPSATQQPEPDPPVGGLGARLMRRKPVERLVAEGGQGEGGSLRRSMGVWQLTMISIGATLGTGIFVVLGEAVPDAGPAVVVSFVIAGLTALFSALSYAELAGTIPVSGSSYSYAYATLGELIAWVCGWCLILEYGVSVAAVAVGWGEYLNELLDGTLGFTIPDVLAAPPGDGGVFNLPALLVVLLAMAFLLGGAKESARANTVMVGVKIAALILFCGVAFTGIRAGNYTPFMPLGMAGVSAAGATLFFSYIGFDAASTAGEEAKNPQRDLPRAIMLSLIIVTALYCLVAAVAVGALPWKKFSGSEAALASIMKDVTGQSFWAVLLAAGAVVAIASVVLTVLYGQTRILFAMSRDGLVPKVFSTVHARTGAPRANTVIVSLFCGVLAAAIPLGQLADATSIGTLFAFALVNIAVIVLRRTRPTMPRTFRVPLSPLFPLIGFALCLWMMGSLQLVTWVVFGAWMALGLVLYFAYGLRRSRLATAEK
>NZ_CP023992.1|WP_069869814.1|8036483_8036690_-|hypothetical-protein
MTTDSLQPPDHSQPGAEPVFRPRDQGGDGERYPLEYCARVWEDFIRALGRIEADFLQRSETTEPGVKA
>NZ_CP023992.1|WP_093705313.1|8035731_8036487_-|DUF2637-domain-containing-protein
MTYTEPRPGGYGPPPTGHRAAPAPPPGERFEAAADYEMNPFPLPDPETIEGRWDLEGDLARLLQTSSAEESVHTTGPIPPLRTPSPAHVRGRGKRRRVRFRLPTMPWLHVISLIFAAVTTVIVAMLSVLGGMISYGPLRYLASPSTSESMAAWWPLLVYGPWLVASLSVLRAALHRRGAAHSWAVVVLFSTIAVFLCVAHAPRNAPSMAVAGLPPVAALVSFHQLVRQITLTSPPRHALPRTRGEPRGMAR
>NZ_CP023992.1|WP_099015566.1|8034159_8035623_+|GuaB1-family-IMP-dehydrogenase-related-protein
MHFLEPGTGRYVKSSPAPYDLTYDDVFMVPSRSAVGSRQGVDLASPDGTGTTIPLVVANMTAIAGRRMAETVARRGGLVVIPQDIPIDVVTDVVRWVKSRHLVLDTPIVLAPTGTVADALSLLPKRAHGAGVVVEDGRPVGVVVESDLTGVDRFTQLSEVMSRELMVLDADIDPQEAFGRLDAAHRKLAPAVDADGKLVGILTRKGALRATLYKPAVDGSGRLRIAAAVGVNGDVEGRTKALIDAGADALVVDTAHGHQESMISALKAVRALGPRVPVVAGNVVSAEGVRDLIEAGADIVKVGVGPGAMCTTRMMTGVGRPQFSAVLECAAEARKSGKHIWADGGVRHPRDVAMALAAGASNVMIGSWFAGTYESPGDLQHTADGRPYKESFGMASARAVRNRTSEESAYERARKGLFEEGISTSRMFLDPARPGVEDLIDSIVAGVRSSCTYAGAGSLEEFHERAVVGVQSAAGYAEGQPLHASWD
>NZ_CP023992.1|WP_167459959.1|8032367_8033849_-|integrin-like-protein
MGAFVPRSSRILTYAIAAGAVATAGFVFPSGATAAAPRTVTSDFNGDGYADLAVGVPDGTVGGQARAGYVNIVWGGPKGVGAYGSIRVTQATPEVPGTPEAGDRFGASVALVDLNGDGIAELLAGVPGEDVTGRGTDAGMVIAIGGSADGPGPGATVLTGPSPSAAYGTSVVAAELTGDDDQEIVIGGTDKVVARVIQGEDSMITTVVAAPMGGRAPVLATGDFDSDGTADLAVAYWTAGNPNTQSHVRLWKWDADRSEMANFWNTDNAGVTALAAGDFDGDGHDDLALGECREIADENIDDPCGPEELAKGGGVHLHYGSPASGSFGSRTQTLNQDTAGVPGVAEDGDRFGAALAVADVNRDGRDDLIVGAPGEAIGSKAGAGAAWLLSGSAQGLLDAGGAATSVSWNQDTPGVPGVAEPGDTFGAAVASGDGNADGVPDVTVGSPGENGSLGAAWLFRSGSADGSTAFSPRTLGLPYLSTAQKYGKPLSSH
>NZ_CP023992.1|WP_099015565.1|8031020_8032223_+|FAD-dependent-monooxygenase
MTNSTPRICVVGAGPAGLTCARVLQGNGIGVTVYDADDAVDSRDPGGTLDLHADSGQIALADAGLLDAFMAQARPEGQAKARRDHHGTVLAEFTPGPGDEAAPEIDRGRLRRLLFDHLRPGTVRWGHRLVRATPLGHGGHRLEFEGGTTVEADLVIGADGAWSKVRPLVSDAAPQHLGVCFLDARFDEVDSRHPEVAGIVGAGHMFSNDNDGRAVILQRNGDGVVRGYIAFRAAPDWHVGAGVDLTDRESIRSYLAREFGHWSAAMRALIVRNDGDYVPRSFWALPAPLTWEHVPGVTLIGDAAHLMAPFGGHGANLAMLDGAELAHAVSRAVGLDEAVAQYESGMFARSGELAVSSNEALVRFFATTDEPHLPPDPEQEHRDYLARAEAYRQERARRAG
>NZ_CP023992.1|WP_099015564.1|8030309_8030894_-|TetR-family-transcriptional-regulator
MTEMGRRERKKAATRQALADAALRLFTERGYDEVGVREIADAADVSVTTLFKHFPDGKEALVFDQDVDREAALVAAVRERPTGQSVPQALHRMLLGEHSRRVHADPRFDDFLRLIDTTPALREYARRMWLRHEYALAAAIADDAGLPADDPGCRALAHFALEAPVLVRGSRDPGTALDRVFDLLGNGWTGARAD
>NZ_CP023992.1|WP_099015563.1|8029785_8030148_-|winged-helix-turn-helix-transcriptional-regulator
MARAATTSDAFNAIAEPQRREILVLLRGGERPVTELARELGMSQPQASKHLRVLREVGLVRARGAGKQRLYGLDARGLRPVHEWLGGFERFWSGSFDRLDEYVQDLKKARQEEPPDDDDQ
>NZ_CP023992.1|WP_099015562.1|8029265_8029802_-|ATPase
MTTTSSGGESEHPSPDREIVISRTISAPRELVFEAYTQVRHLSRWWGPEGFSTTTRSFEFRVGGIWDFVMHGPDGTDYQEWITWREIVPPERIALLHGESRDDPNAFESVLAFEPVGDETRIVMRTVFPTKELRDEAVEKYHAIEGGEQTLGNLAAYVAELTQNDTGRNETTPNGAKS
>NZ_CP023992.1|WP_069869817.1|8039320_8040118_+|carbon-nitrogen-hydrolase-family-protein
MPPLRTALLQNSGHPGDPAGNLKVLDEAAARAAADGAGLLVTAEMFLTGYAIGGGVRDLAEPADGPSGRAVADIAAAHGLAILYGYPERHAGAVHNSARLVGADGTELANYRKTHLYGCFERASFTPGETPVVQATVGELTVGILVCYDVEFPENVRAHALAGTDLLLVPTAQMHPFEFVAESLIPVRAFESQMYIAYVNRSGPEGEFDFVGLSCLAGPDGATCLRAGRGEELLLGDVDPKLLTTSRRINPYLRDRRPGLYTSLG
>NZ_CP023992.1|WP_099015568.1|8040185_8041895_+|FAD-dependent-oxidoreductase
MTSTVPTAVHDQQEERALDALPPVTMFGPDFPYAYDDYLAHPAGLGQIPATEHGSEVAVVGGGLSGVVTAYELMKMGLRPVVYEADRIGGRLRTVGFDGCDDSLTAEMGAMRFPPSSTALQHYIDLVGLKTRPFPNPLAPDTPSTVVDLKGESHYARTIDDLPPVYREVADAWSACLEEGADFSDMNRAIRERDVPRIREIWSRLVEKLDNQTFYGFLCDSTAFTSFRHREIFGQVGFGTGGWDTDFPNSILEILRVVYTEADDHHRGIVGGSQQLPLRLWEREPGKIVHWPQGTSLASLHGGAPRPAATRLHRAAGDRVVVTDASGDIRSYRAVVFTAQSWMLLSQIDCDDSLFPIDHWTAIERTHYMESSKLFVPVDRPFWLDEDETTGRDTMSMTLTDRMTRGTYLLDDGPDRPAVICLSYTWCDDSLKWLPLSANERMEVMLKSLSEIYPNVDIRKHIIGSPITVSWENEPYFMGAFKANLPGHYRYQRRLFTHFMQDRLPADKRGVFLAGDDISWTAGWAEGAVQTALNAVWGVMHRFGGATDPKNPGPGDLYEEIAPVELPED
>NZ_CP023992.1|WP_167460047.1|8041953_8042649_-|hypothetical-protein
MPTHTRPAPRTVRSAVARMSALGAALPPGDGVAVFNGVYLSVTEEVGRRLVDGYFQDPSATEELDARFAGRYLAAVDAVATGGRPPACWRPLFQSRRHPGVRPVQFALAGINAHIGHDLALALLDTCRARGVEPDALEGDFDRIGALLTGMEERIREELMPGPDLLDVADPLTHLMGSWSLEKAREAAWAAFRALWGLRGLPELAAEFAERVDTTVGLVGRFLLTPLPSAP
>NZ_CP023992.1|WP_099015569.1|8042744_8043629_-|NAD(P)-dependent-oxidoreductase
MPLILVTGVTGQVGRRFTKRLLEQAAAGTEVRVLVRDEERGAPFAALGAQLSVGDLREEKDLRRAMEGAHAVVNIAAAFRGVPDEEAWAVNRDAAVALGRAAVEAGTSRFLQVSTNLVYGVSRGRPFTEDDESRPGGLLWGAYPASKAEAERELLALHREHGLDLRIGSLAFVYGDGDPHVDNFLPHSRDWAGDQRLAMVHHADATAALLRLLRAPGGSAGGSVSGRKYNIVDDAPATVVEIHQLKGAPLPEGMTERTTDDPWFGITSNRRLRDELGWRPLYPSMWTARDAGAL
>NZ_CP023992.1|WP_069869821.1|8043761_8044628_+|helix-turn-helix-domain-containing-protein
MHRTELADFLRRCRARLGPTEVGLTPGPRRRTPGLRREEVAQLAGMSPDYYTRLEQARGPRPSRQMLTALARALRLTDDERDYLFHLVGEEPPRNRGTSGHVRPGLLRVLDRLYDTPAQVITDWGEVLAQNAMAAALVGDITARPPGDRNIIRSFFTRRDDTPGIFPSEEIEEHARLHVATLRAVLAARPDDPGPASLVAELLAGSEEFAAMWADHEVAIRHSTVKRFTHPVVGTMELDCEVLLSSEHAQRLIVHTARPGSESAERLELLRVVGLQNLAPRDEESPAG
>NZ_CP023992.1|WP_093702616.1|8044673_8046056_-|nitrate-reductase
MGLGVRWTLHGDGRTPAPGAVVKPDERLSWPRTVGLGAQHVVAMFGASFVAPVLMGLDPNLAIMMSGVATVLFLVATRGRIPSYLGCSLSFVGVAAAIRAQGGGSGAVTGAILVVGGVLLLSGLAVRRFGARIIHAAMPPVVTGAVVMLIGFNLAPVTAGTYWPADQWTALLTMLVTGAAVVCLRGFWSRIAIFLGLVFGYAVSWIFDRVFGKIHSVGGGGRITDHWRLDLSAVGKADWIGLPSLHGPSFHWSAVLVALPVVIALIAENAGHVKAVGEMIGDPLDDQLGTAIAADGAATMISTSVGGPANTTYSENIGVMAATRVYSTAAYWAAAGFALLFGLCPKFGAVVAAVPGGVLGGITVILYGMIGLLGAQIWVHNKVDLRNPLNLVPVAAGVIIGVGGVSLKISDNFELGGIALGTIVVLLGYHVLRALAPAHLKRQEPLLDAGTSEYDNERPA
>NZ_CP023992.1|WP_099015570.1|8046124_8047009_-|isocitrate-lyase/phosphoenolpyruvate-mutase-family-protein
MTDDTGDGPAPDRHTAFHRLHHADRPLLLPNAWDHASAAALVRRGFPAIGTTSLGVAAAAGLPDATGAAREGTLALARGLARLPALVSVDIEGGFGERPEEVAAATAELDRAGVVGVNIEDGRPDGTLAPLARQCAVIAAVKERVPRLFVNARTDTHWLAALDGGTPPSLSTTAERIEAYLRAGADGIFVPALTDEQDIGALADDLGETPLNILFAPGRHTYESLAELGVRRISCGSLLFRAALDRAVELAWTIAHPRPEAGNGLDRAADLLSYAEAQSLAGDFTQDPAEATPA
>NZ_CP023992.1|WP_099015571.1|8047095_8048328_-|MFS-transporter
MGRLKETGASEMRPVRRARVAVATVFAVHGAVTGNFATRIPWIQERLDLSAGQLGLALAFPAIGASLAMPLAGRISHRFGARAALRGLLALWTAWLVMPPLAPGLVWLCGVLLVFGATAGTSDVAMNALGVEVENRLGRSIMSGLHGMWSVGALTGSAAGTVAAHAGADARLHLGIAAAVLTVLGTVVCHWVLDLRSTPEEHPPPRFALPPRSALIIGAVGFCAVFAEGASLDWSAVYLRDVLDTSPGLAAACTTAFSCTMAGARLVGDAVVGRFGAVRTVRTGGVLATAGGLLVVTASTPALAIAGFGLIGLGIAVVVPLAFAAAGRSGPAPSQAITGVATITYTSGLIAPAAMGSIADLTSLTISFCLVTTLALGLVAGAGVLRIPARTDAAGSDPHSDPSTSRASLP
>NZ_CP023992.1|WP_099017184.1|8048473_8049700_+|ROK-family-transcriptional-regulator
MTSTSLSAVGRTASPSTARAINDGLALHLLKDKGPLTAGQLKSLTGLSRPTIADLVERLRQTGLVAVVGEAGAERRGPNARLYGIVADSAHVAGVDVRTDSVAVCLADLLGRTLVEESLPVAPDVDPAHTVAAAVALVERAAERAGAARLHHIGIGAPGLIDPATGELNSTGALPSWHRELATALHDGLAAPVLLENEVNLAAVAEQRLGAVRDRDTFVLLWLGHGIGAAVVLDRVLRRGASGGTGEIGFLPVPGTSELPSATSCDGGFHSLVSGGAVCELAQQHGLVAAAYGERGAGAEGSGAAEAVIRAALGAGERGEAFLDALAARIALGVAAICAVLDPGCAVLGGEVGRAGGDGLAGRVEDHVARLSPLRTRVRAGAVGGGGVLRGAVLMALDATQNELFGAP
>NZ_CP023992.1|WP_099015572.1|8049827_8051132_+|alginate-lyase-family-protein
MGTPPAGRGRLARAIIATAALLAVLAIPSAPSAQGAERAPHAGPVPRTVVLDGPRLSLTKLKLQLGDEKLRRTVRDLTTRADRWMEQGPWTVTDKDQVPPSGDKHDYFSQAPYWWPSRPKTEDNPYGCPYVQKDGQRNPDVDKMTDRPEVGKVFESAYELSLAWYYTGERAYAEHAADILRTWFVTPATRMNPNLDHAQFIPCQYDGRSIGIIDFSQAFTSLLDAAALLDTGAPGWSKTDHEGFRGWNEQFLDWLVNSDFGKEEGAAENNHGTFYDMQIAAIATAVGDRDLARRVLRDARAKRIDTQIAADGTQPQELARTRSFHYSTFNLVAYTRMAAIGEHIGVDLWHYTGPGGANLFKAVDVLLPAATGAEPWPYPELDFRAYAASDIVHAAADAGDREARAAVDKLQAPPGGDLWALRPAVEQLDSIAQG

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP023992_3	3.1\|2766000\|19\|NZ_CP023992\|CRISPRCasFinder	2766000-2766018	19	NZ_CP023992.1	6929614-6929632	2	0.895
NZ_CP023992_3	3.1\|2766000\|19\|NZ_CP023992\|CRISPRCasFinder	2766000-2766018	19	NZ_CP023992.1	10019626-10019644	2	0.895
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	914801-914846	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	1052898-1052943	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	1282506-1282551	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	3892901-3892946	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	6429073-6429118	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	6636615-6636660	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	8271210-8271255	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	8374308-8374353	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	8470879-8470924	2	0.957
NZ_CP023992_14	14.1\|6268335\|46\|NZ_CP023992\|CRISPRCasFinder	6268335-6268380	46	NZ_CP023992.1	8888688-8888733	2	0.957

1. spacer 3.1|2766000|19|NZ_CP023992|CRISPRCasFinder matches to position: 6929614-6929632, mismatch: 2, identity: 0.895

gccgaagtcgccaccgttc	CRISPR spacer
gccgaattcggcaccgttc	Protospacer
****** *** ********

2. spacer 3.1|2766000|19|NZ_CP023992|CRISPRCasFinder matches to position: 10019626-10019644, mismatch: 2, identity: 0.895

gccgaagtcgccaccgttc	CRISPR spacer
gccgaagtcgacaccggtc	Protospacer
********** ***** **

3. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 914801-914846, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatatgcggctccgccgcgcgggcgcgaccagccacgac	Protospacer
*****.********************.*******************

4. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 1052898-1052943, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatgtgcggctccgccgcgtgggcgcgaccagccacgac	Protospacer
*****.****.***********************************

5. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 1282506-1282551, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatgtgcggctccgccgcgtgggcgcgaccagccacgac	Protospacer
*****.****.***********************************

6. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 3892901-3892946, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgccgatatgcggctccgccgcgtgggcgcggccggccacgac	Protospacer
**********************************.**.********

7. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 6429073-6429118, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatatgcggctccgccgcgcgggcgcgaccagccacgac	Protospacer
*****.********************.*******************

8. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 6636615-6636660, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatgtgcggctccgccgcgtgggcgcgaccagccacgac	Protospacer
*****.****.***********************************

9. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 8271210-8271255, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatatgcggctccgccgcgcgggcgcgaccagccacgac	Protospacer
*****.********************.*******************

10. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 8374308-8374353, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgccgatgtgcggctccgccgcgcgggcgcgaccagccacgac	Protospacer
**********.***************.*******************

11. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 8470879-8470924, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatgtgcggctccgccgcgtgggcgcgaccagccacgac	Protospacer
*****.****.***********************************

12. spacer 14.1|6268335|46|NZ_CP023992|CRISPRCasFinder matches to position: 8888688-8888733, mismatch: 2, identity: 0.957

ctgtgccgatatgcggctccgccgcgtgggcgcgaccagccacgac	CRISPR spacer
ctgtgtcgatgtgcggctccgccgcgtgggcgcgaccagccacgac	Protospacer
*****.****.***********************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP023992_11	11.1\|4536402\|24\|NZ_CP023992\|CRISPRCasFinder	4536402-4536425	24	NZ_CP032324	Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence	94403-94426	3	0.875
NZ_CP023992_11	11.1\|4536402\|24\|NZ_CP023992\|CRISPRCasFinder	4536402-4536425	24	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	815677-815700	3	0.875
NZ_CP023992_11	11.1\|4536402\|24\|NZ_CP023992\|CRISPRCasFinder	4536402-4536425	24	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	244196-244219	3	0.875
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP020471	Rhodobacter blasticus strain 28/5 plasmid pRsa, complete sequence	116366-116390	3	0.88
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	MN096358	Microbacterium phage LeeroyJenkins, complete genome	9273-9297	3	0.88
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	MN096357	Microbacterium phage WaterT, complete genome	9099-9123	3	0.88
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	MT818426	Microbacterium phage Lifes, complete genome	8825-8849	3	0.88
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP019037	Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence	66203-66227	3	0.88
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1237589-1237613	3	0.88
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	476703-476727	3	0.88
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	575486-575510	3	0.88
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1571064-1571088	3	0.88
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	1509552-1509576	3	0.88
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	1505547-1505571	3	0.88
NZ_CP023992_13	13.2\|5997807\|25\|NZ_CP023992\|CRISPRCasFinder	5997807-5997831	25	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	65156-65180	4	0.84
NZ_CP023992_13	13.2\|5997807\|25\|NZ_CP023992\|CRISPRCasFinder	5997807-5997831	25	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	1687975-1687999	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP028969	Aminobacter sp. MSH1 plasmid pUSP1, complete sequence	162145-162169	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP026266	Aminobacter sp. MSH1 plasmid pAM01, complete sequence	159439-159463	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1322176-1322200	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1918858-1918882	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	199669-199693	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1388935-1388959	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1349678-1349702	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	796232-796256	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	796232-796256	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	796232-796256	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	796232-796256	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	796232-796256	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	796234-796258	4	0.84
NZ_CP023992_13	13.3\|5997855\|25\|NZ_CP023992\|CRISPRCasFinder	5997855-5997879	25	MT770738	Rhizobium phage B1VFA, complete genome	93177-93201	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4468435-4468459	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	2032185-2032209	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP020441	Paracoccus yeei strain FDAARGOS_252 plasmid unnamed1, complete sequence	50852-50876	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP044080	Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence	36096-36120	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP044082	Paracoccus yeei strain FDAARGOS_643 plasmid unnamed4, complete sequence	163184-163208	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP031080	Paracoccus yeei strain CCUG 32053 plasmid pYEE2, complete sequence	54821-54845	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP024424	Paracoccus yeei strain TT13 plasmid pTT13-2, complete sequence	48325-48349	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP020440	Paracoccus yeei strain FDAARGOS_252 plasmid unnamed2, complete sequence	159491-159515	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	330978-331002	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NC_013857	Azospirillum sp. B510 plasmid pAB510c, complete sequence	579359-579383	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	187636-187660	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP031082	Paracoccus yeei strain CCUG 32053 plasmid pYEE4, complete sequence	17364-17388	4	0.84
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	1908084-1908108	4	0.84
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	NZ_CP045373	Sulfitobacter sp. THAF37 plasmid pTHAF37_a, complete sequence	136727-136751	4	0.84
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	MN693987	Marine virus AFVG_250M285, complete genome	177-201	4	0.84
NZ_CP023992_16	16.2\|7336721\|25\|NZ_CP023992\|CRISPRCasFinder	7336721-7336745	25	MN693987	Marine virus AFVG_250M285, complete genome	40123-40147	4	0.84
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NC_008537	Arthrobacter sp. FB24 plasmid 1, complete sequence	63445-63469	5	0.8
NZ_CP023992_13	13.4\|5997903\|25\|NZ_CP023992\|CRISPRCasFinder	5997903-5997927	25	NZ_CP042998	Aquisphaera giovannonii strain OJF2 plasmid pOJF2_1, complete sequence	100068-100092	5	0.8
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	2131802-2131834	6	0.818
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	KM659090	Achromobacter sp. LM16 plasmid pLM16A1, complete sequence	11208-11240	8	0.758
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	NZ_KP873172	Pseudomonas aeruginosa PAO1 plasmid pAMBL1, complete sequence	14536-14568	8	0.758
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	NZ_CP020898	Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRetBra5b, complete sequence	30240-30272	8	0.758
NZ_CP023992_6	6.1\|3501772\|32\|NZ_CP023992\|CRISPRCasFinder	3501772-3501803	32	NZ_CP034999	Rhizobium acidisoli strain FH23 plasmid pRapFH23a, complete sequence	440214-440245	9	0.719
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	860735-860767	10	0.697
NZ_CP023992_17	17.1\|7509820\|33\|NZ_CP023992\|CRISPRCasFinder	7509820-7509852	33	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1676987-1677019	10	0.697

1. spacer 11.1|4536402|24|NZ_CP023992|CRISPRCasFinder matches to NZ_CP032324 (Azospirillum brasilense strain MTCC4035 plasmid p3, complete sequence) position: , mismatch: 3, identity: 0.875

ccgccctacgccgccgtccccgca	CRISPR spacer
ccggcctacgccgccgaccccgcc	Protospacer
*** ************ ******

2. spacer 11.1|4536402|24|NZ_CP023992|CRISPRCasFinder matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 3, identity: 0.875

ccgccctacgccgccgtccccgca	CRISPR spacer
ccgccctacggcgccggccccgcg	Protospacer
********** ***** ******.

3. spacer 11.1|4536402|24|NZ_CP023992|CRISPRCasFinder matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 3, identity: 0.875

ccgccctacgccgccgtccccgca	CRISPR spacer
ccggcctacgccgccgaccccgcc	Protospacer
*** ************ ******

4. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP020471 (Rhodobacter blasticus strain 28/5 plasmid pRsa, complete sequence) position: , mismatch: 3, identity: 0.88

ctcggcaggcggttcgcccggcggt	CRISPR spacer
ctcggaaggcggttcgcccggcaga	Protospacer
***** ****************.*

5. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to MN096358 (Microbacterium phage LeeroyJenkins, complete genome) position: , mismatch: 3, identity: 0.88

ctcggcaggcggttcgcccggcggt	CRISPR spacer
cccggctggcggttcgcccggaggt	Protospacer
*.**** ************** ***

6. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to MN096357 (Microbacterium phage WaterT, complete genome) position: , mismatch: 3, identity: 0.88

ctcggcaggcggttcgcccggcggt	CRISPR spacer
cccggctggcggttcgcccggaggt	Protospacer
*.**** ************** ***

7. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to MT818426 (Microbacterium phage Lifes, complete genome) position: , mismatch: 3, identity: 0.88

ctcggcaggcggttcgcccggcggt	CRISPR spacer
cccggctggcggttcgcccggaggt	Protospacer
*.**** ************** ***

8. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP019037 (Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence) position: , mismatch: 3, identity: 0.88

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ggcggcacgcggcccgcccggcgcc	Protospacer
  ***** *****************

9. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 3, identity: 0.88

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
gtcggccggctgcccgcccggcgcc	Protospacer
 ***** *** **************

10. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 3, identity: 0.88

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ttcgggaggcggcgcgcccggcgcc	Protospacer
.**** ******* ***********

11. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 3, identity: 0.88

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
gtcggccggctgcccgcccggcgcc	Protospacer
 ***** *** **************

12. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 3, identity: 0.88

accgaatgccgcaccgggcgccgca	CRISPR spacer
accgaaatccgcaccgggcgccgga	Protospacer
******  *************** *

13. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 3, identity: 0.88

accgaatgccgcaccgggcgccgca	CRISPR spacer
accgaaatccgcaccgggcgccgga	Protospacer
******  *************** *

14. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 3, identity: 0.88

accgaatgccgcaccgggcgccgca	CRISPR spacer
accgaaatccgcaccgggcgccgga	Protospacer
******  *************** *

15. spacer 13.2|5997807|25|NZ_CP023992|CRISPRCasFinder matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 4, identity: 0.84

cccctctgccgacttgtccggtgct	CRISPR spacer
ttcatctgccgacttgtccagtgct	Protospacer
..* ***************.*****

16. spacer 13.2|5997807|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 4, identity: 0.84

cccctctgccgacttgtccggtgct	CRISPR spacer
gccgtctgccgacatgtccggtgca	Protospacer
 ** ********* **********

17. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP028969 (Aminobacter sp. MSH1 plasmid pUSP1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
ttcggccgccggttcgcccggcggc	Protospacer
.***** * ***************.

18. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP026266 (Aminobacter sp. MSH1 plasmid pAM01, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
ttcggccgccggttcgcccggcggc	Protospacer
.***** * ***************.

19. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

20. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

21. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
gccggaaggcggtccgcccggcggt	Protospacer
 .*** *******.***********

22. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

23. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

24. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

25. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

26. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

27. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

28. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

29. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
tgcgccaggcggttcgcctggcggt	Protospacer
. ** *************.******

30. spacer 13.3|5997855|25|NZ_CP023992|CRISPRCasFinder matches to MT770738 (Rhizobium phage B1VFA, complete genome) position: , mismatch: 4, identity: 0.84

ctcggcaggcggttcgcccggcggt	CRISPR spacer
aacggcaagcggttcgcccagcggt	Protospacer
  *****.***********.*****

31. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
tgcagcaggcggcccgcgcggcgcc	Protospacer
. *.************* *******

32. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ttgggcaggcggcgcgcccggcgct	Protospacer
.* ********** **********.

33. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP020441 (Paracoccus yeei strain FDAARGOS_252 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
tccggcaggcggccagcccgtcgcc	Protospacer
..************ ***** ****

34. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP044080 (Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
tccggcaggcggccagcccgtcgcc	Protospacer
..************ ***** ****

35. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP044082 (Paracoccus yeei strain FDAARGOS_643 plasmid unnamed4, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ccttgccggcggcccgcccggcgcc	Protospacer
*.. ** ******************

36. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP031080 (Paracoccus yeei strain CCUG 32053 plasmid pYEE2, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ccttgccggcggcccgcccggcgcc	Protospacer
*.. ** ******************

37. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP024424 (Paracoccus yeei strain TT13 plasmid pTT13-2, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ccttgccggcggcccgcccggcgcc	Protospacer
*.. ** ******************

38. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP020440 (Paracoccus yeei strain FDAARGOS_252 plasmid unnamed2, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ccttgccggcggcccgcccggcgcc	Protospacer
*.. ** ******************

39. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
atgcgcaggcggccagcccggcgcc	Protospacer
 *  ********** **********

40. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NC_013857 (Azospirillum sp. B510 plasmid pAB510c, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
tccggcaggcggcctgcccggcccc	Protospacer
..************.******* **

41. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ttcggccgccggcccgcccggcgca	Protospacer
.***** * ***************

42. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP031082 (Paracoccus yeei strain CCUG 32053 plasmid pYEE4, complete sequence) position: , mismatch: 4, identity: 0.84

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
tccggcaggcggccagcccgtcgcc	Protospacer
..************ ***** ****

43. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.84

accgaatgccgcaccgggcgccgca	CRISPR spacer
gccgaatgccgcgccgggcggcgcg	Protospacer
.***********.******* ***.

44. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP045373 (Sulfitobacter sp. THAF37 plasmid pTHAF37_a, complete sequence) position: , mismatch: 4, identity: 0.84

accgaatgccgcaccgggcgccgca	CRISPR spacer
cctgaatgccgcaccggtcgccgcg	Protospacer
 *.************** ******.

45. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to MN693987 (Marine virus AFVG_250M285, complete genome) position: , mismatch: 4, identity: 0.84

accgaatgccgcaccgggcgccgca	CRISPR spacer
aggcaatgccgcaccgggtgccgca	Protospacer
*   **************.******

46. spacer 16.2|7336721|25|NZ_CP023992|CRISPRCasFinder matches to MN693987 (Marine virus AFVG_250M285, complete genome) position: , mismatch: 4, identity: 0.84

accgaatgccgcaccgggcgccgca	CRISPR spacer
aggcaatgccgcaccgggtgccgca	Protospacer
*   **************.******

47. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NC_008537 (Arthrobacter sp. FB24 plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.8

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ggcggcaggcggcccgcgcggcggg	Protospacer
  *************** *****

48. spacer 13.4|5997903|25|NZ_CP023992|CRISPRCasFinder matches to NZ_CP042998 (Aquisphaera giovannonii strain OJF2 plasmid pOJF2_1, complete sequence) position: , mismatch: 5, identity: 0.8

ctcggcaggcggcccgcccggcgcc	CRISPR spacer
ctcggcaggaggcccgcccggacga	Protospacer
********* ***********

49. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.818

acggtcgatgcggacggcctcaaggc--ccacgga	CRISPR spacer
gtggtcgatgcggacgccctcatggcaaccacg--	Protospacer
..************** ***** ***  *****

50. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to KM659090 (Achromobacter sp. LM16 plasmid pLM16A1, complete sequence) position: , mismatch: 8, identity: 0.758

acggtcgatgcggacggcctcaaggcccacgga-	CRISPR spacer
aatgtcgatgcggtcggcctccagg-ccgcgcct	Protospacer
*  ********** ******* *** **.**

51. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to NZ_KP873172 (Pseudomonas aeruginosa PAO1 plasmid pAMBL1, complete sequence) position: , mismatch: 8, identity: 0.758

acggtcgatgcggacggcctcaaggcccacgga-	CRISPR spacer
aatgtcgatgcggtcggcctccagg-ccgcgcct	Protospacer
*  ********** ******* *** **.**

52. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to NZ_CP020898 (Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRetBra5b, complete sequence) position: , mismatch: 8, identity: 0.758

acggtcgatgcggacggcctcaaggcccacgga	CRISPR spacer
gtgatccttgcggaccgcctcaaggccaacggt	Protospacer
..*.**  ******* *********** ****

53. spacer 6.1|3501772|32|NZ_CP023992|CRISPRCasFinder matches to NZ_CP034999 (Rhizobium acidisoli strain FH23 plasmid pRapFH23a, complete sequence) position: , mismatch: 9, identity: 0.719

ccaccggccacgggctccgccccaagaccctg	CRISPR spacer
ccaccggccaccggctccgcaccctcggcaag	Protospacer
*********** ******** **   . *  *

54. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 10, identity: 0.697

acggtcgatgcggacggcctcaaggcccacgga	CRISPR spacer
ctgcgcgatgaggacggccgcaaggcccatccg	Protospacer
 .*  ***** ******** *********.  .

55. spacer 17.1|7509820|33|NZ_CP023992|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 10, identity: 0.697

acggtcgatgcggacggcctcaaggcccacgga	CRISPR spacer
ctgcgcgatgaggacggccgcaaggcccatccg	Protospacer
 .*  ***** ******** *********.  .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

4559540 : 4615675

Streptomyces_phage(25.0%)

holin,transposase,tRNA,protease

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_069860863.1\|4559540_4562066_-\|protease	ATP-dependent Clp protease ATP-binding subunit	K4FB40	Cronobacter_phage	1.0e-131	40.7
WP_069860864.1\|4562541_4563135_+	hypothetical protein	NA	NA	NA	NA
WP_069860865.1\|4563140_4563476_-	Lsr2 family protein	K4NXG4	Streptomyces_phage	6.2e-13	42.2
WP_069860866.1\|4563696_4564218_-	amino-acid N-acetyltransferase	NA	NA	NA	NA
WP_079258096.1\|4564240_4564636_-	CopY family transcriptional repressor	NA	NA	NA	NA
WP_069860868.1\|4564829_4565012_-	hypothetical protein	NA	NA	NA	NA
WP_079152807.1\|4565133_4565949_-	hypothetical protein	NA	NA	NA	NA
WP_020870373.1\|4566317_4567115_-	type III pantothenate kinase	NA	NA	NA	NA
WP_069860871.1\|4567118_4568159_-	carboxylating nicotinate-nucleotide diphosphorylase	NA	NA	NA	NA
WP_099016990.1\|4568155_4569958_-	L-aspartate oxidase	NA	NA	NA	NA
WP_099014163.1\|4570023_4570995_-	pantoate--beta-alanine ligase	NA	NA	NA	NA
WP_069860872.1\|4570991_4571927_-	DUF2520 domain-containing protein	NA	NA	NA	NA
WP_099014164.1\|4572074_4573358_+	threonine aldolase	NA	NA	NA	NA
WP_099014166.1\|4573757_4574909_-\|transposase	IS200/IS605 family element transposase accessory protein TnpB	I4AZM3	Saccharomonospora_phage	9.4e-61	45.0
WP_099014167.1\|4575257_4575971_-	response regulator transcription factor	NA	NA	NA	NA
WP_099014168.1\|4576065_4577262_-	sensor histidine kinase	NA	NA	NA	NA
WP_099014169.1\|4577370_4578393_+	hypothetical protein	NA	NA	NA	NA
WP_099014170.1\|4578748_4579891_+	NADH-quinone oxidoreductase subunit D	NA	NA	NA	NA
WP_167459921.1\|4579986_4581132_-	hypothetical protein	NA	NA	NA	NA
WP_099014172.1\|4581273_4582233_-	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_069860883.1\|4582437_4583175_-	ABC transporter permease subunit	NA	NA	NA	NA
WP_069860884.1\|4583174_4583858_-	ABC transporter permease	NA	NA	NA	NA
WP_099014173.1\|4583999_4585157_+\|holin	betaine/proline/choline family ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	1.4e-24	33.5
WP_099014174.1\|4585299_4586433_-	esterase	NA	NA	NA	NA
WP_079258108.1\|4586601_4588434_+	DUF2156 domain-containing protein	NA	NA	NA	NA
WP_079258109.1\|4588469_4589348_+	dihydropteroate synthase	A0A0B5J4J5	Pandoravirus	1.0e-22	32.9
WP_069860889.1\|4589344_4589830_+	nuclear transport factor 2 family protein	NA	NA	NA	NA
WP_079152810.1\|4590029_4590398_+	dihydroneopterin aldolase	NA	NA	NA	NA
WP_099014175.1\|4590394_4590988_+	2-amino-4-hydroxy-6- hydroxymethyldihydropteridine diphosphokinase	NA	NA	NA	NA
WP_069860892.1\|4591049_4591550_+	DUF3180 domain-containing protein	NA	NA	NA	NA
WP_069860893.1\|4591616_4592222_-	GTP cyclohydrolase I FolE	E7DN69	Pneumococcus_phage	5.1e-42	51.1
WP_069860894.1\|4592349_4594392_-\|protease	ATP-dependent zinc metalloprotease FtsH	G8DDJ2	Micromonas_pusilla_virus	1.5e-106	44.5
WP_069861363.1\|4594635_4595175_-	hypoxanthine phosphoribosyltransferase	A0A1V0SEQ1	Hokovirus	3.0e-09	30.1
WP_079258111.1\|4595236_4596382_-\|tRNA	tRNA lysidine(34) synthetase TilS	NA	NA	NA	NA
WP_099014176.1\|4596578_4597721_-\|protease	zinc-dependent metalloprotease	NA	NA	NA	NA
WP_099014177.1\|4597808_4599407_-	D-alanyl-D-alanine carboxypeptidase/D-alanyl-D-alanine-endopeptidase	NA	NA	NA	NA
WP_069860898.1\|4599493_4599985_+	inorganic diphosphatase	A0A2H4J8U1	uncultured_Caudovirales_phage	5.9e-28	45.2
WP_069860899.1\|4600113_4601817_-	threonine/serine exporter family protein	NA	NA	NA	NA
WP_079258114.1\|4602027_4602735_-	hypothetical protein	NA	NA	NA	NA
WP_099014178.1\|4602960_4603719_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_099016991.1\|4603844_4604552_+	leucine efflux protein LeuE	NA	NA	NA	NA
WP_069860902.1\|4604619_4606029_+	glutamate decarboxylase	NA	NA	NA	NA
WP_099014179.1\|4606066_4607656_-	hypothetical protein	NA	NA	NA	NA
WP_069860904.1\|4607728_4608514_-	ABC transporter permease	NA	NA	NA	NA
WP_099014180.1\|4608510_4609560_-	ATP-binding cassette domain-containing protein	A0A2H4PQG7	Staphylococcus_phage	1.3e-21	30.0
WP_099014181.1\|4609707_4610337_-	PadR family transcriptional regulator	NA	NA	NA	NA
WP_093703932.1\|4610492_4611059_-	DinB family protein	NA	NA	NA	NA
WP_099014182.1\|4611172_4612630_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_069860908.1\|4612721_4613585_-	helix-turn-helix domain-containing protein	A0A1J0MCL6	Streptomyces_phage	5.8e-39	38.9
WP_069861367.1\|4613911_4614379_+	ATP-binding protein	A0A1V0E640	Streptomyces_phage	3.4e-09	32.9
WP_069860909.1\|4614523_4615675_-\|protease	site-2 protease family protein	NA	NA	NA	NA

DBSCAN-SWA_2

7912810 : 7925870

Streptomyces_phage(100.0%)

capsid,terminase,portal

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_099015514.1\|7912810_7913950_-	methyltransferase domain-containing protein	A0A1J0MC37	Streptomyces_phage	5.0e-30	32.4
WP_099015515.1\|7913946_7914819_-	radical SAM protein	NA	NA	NA	NA
WP_099017175.1\|7915453_7915663_-	hypothetical protein	NA	NA	NA	NA
WP_099015517.1\|7915949_7917179_-	helix-turn-helix transcriptional regulator	A0A0K1Y5U6	Streptomyces_phage	2.1e-18	24.4
WP_099015518.1\|7917300_7917558_-	hypothetical protein	A0A1V0E647	Streptomyces_phage	2.4e-09	60.9
WP_107528534.1\|7918544_7919009_-	hypothetical protein	A0A1V0E621	Streptomyces_phage	2.2e-48	77.1
WP_167459955.1\|7919740_7919902_-	hypothetical protein	A0A1J0MCN3	Streptomyces_phage	5.9e-14	75.0
WP_099017176.1\|7919906_7921841_-\|capsid	phage capsid protein	A0A1J0MCU0	Streptomyces_phage	2.2e-259	66.8
WP_167459956.1\|7922189_7923665_-\|portal	phage portal protein	A0A1J0MCN7	Streptomyces_phage	2.2e-248	85.0
WP_142881340.1\|7923717_7924143_+	hypothetical protein	NA	NA	NA	NA
WP_099015519.1\|7924195_7924648_+	hypothetical protein	NA	NA	NA	NA
WP_099015520.1\|7924613_7925870_-\|terminase	PBSX family phage terminase large subunit	A0A1J0MCH4	Streptomyces_phage	9.8e-221	90.5

DBSCAN-SWA_3

9032455 : 9094178

Staphylococcus_phage(30.0%)

tail,plate,integrase,transposase

attL 9030464:9030483|attR 9087090:9087109

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
9030464:9030483	attL	NA	NA	NA	NA
WP_099015935.1\|9032455_9033664_+\|transposase	IS200/IS605 family element transposase accessory protein TnpB	A0A0R8V9X2	Thermobifida_phage	2.5e-157	76.5
WP_167460054.1\|9034776_9036390_+	AMP-binding protein	A0A2H4PQU7	Staphylococcus_phage	4.4e-64	34.9
WP_069860581.1\|9036556_9036925_-	arsenate reductase family protein	NA	NA	NA	NA
WP_069860582.1\|9037047_9037353_+	hypothetical protein	NA	NA	NA	NA
WP_069860583.1\|9037730_9038210_+	hypothetical protein	NA	NA	NA	NA
WP_159033486.1\|9038306_9038870_+	hypothetical protein	NA	NA	NA	NA
WP_099015938.1\|9038940_9039693_+	DUF305 domain-containing protein	NA	NA	NA	NA
WP_099015939.1\|9039770_9040706_-	M56 family metallopeptidase	NA	NA	NA	NA
WP_069860587.1\|9040702_9041071_-	BlaI/MecI/CopY family transcriptional regulator	NA	NA	NA	NA
WP_069860588.1\|9041230_9041761_+	TerD family protein	NA	NA	NA	NA
WP_099015940.1\|9041865_9042723_-	hypothetical protein	NA	NA	NA	NA
WP_099015941.1\|9042722_9043991_-	VWA domain-containing protein	NA	NA	NA	NA
WP_099015942.1\|9044157_9046971_+	alpha/beta fold hydrolase	A0A2H4PQG7	Staphylococcus_phage	5.7e-27	33.8
WP_093700553.1\|9046967_9047822_+	ABC transporter permease subunit	NA	NA	NA	NA
WP_099015943.1\|9047903_9049088_-	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_167459969.1\|9049763_9052103_+	glycosyltransferase	A0A1V0S9E5	Catovirus	2.2e-32	32.1
WP_099015944.1\|9052099_9053362_+	acyltransferase	NA	NA	NA	NA
WP_099015945.1\|9053527_9054136_+	extensin	NA	NA	NA	NA
WP_099015946.1\|9054177_9055071_-	lysozyme	I3VYU7	Thermoanaerobacterium_phage	8.5e-17	35.4
WP_099015947.1\|9055153_9055801_-	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_099015948.1\|9055811_9057974_-	xanthine dehydrogenase family protein molybdopterin-binding subunit	NA	NA	NA	NA
WP_099015949.1\|9057970_9058972_-	xanthine dehydrogenase family protein subunit M	NA	NA	NA	NA
WP_069860599.1\|9058968_9059562_-	2Fe-2S iron-sulfur cluster binding domain-containing protein	NA	NA	NA	NA
WP_099015950.1\|9059613_9060765_+	XdhC family protein	NA	NA	NA	NA
WP_099017238.1\|9060873_9062187_+	MFS transporter	NA	NA	NA	NA
WP_099015951.1\|9062373_9063828_-	NADP-dependent phosphogluconate dehydrogenase	E3SIC7	Synechococcus_phage	1.4e-32	30.2
WP_159033487.1\|9064482_9065082_-	TetR family transcriptional regulator	NA	NA	NA	NA
WP_099015953.1\|9065190_9066684_+	MFS transporter	NA	NA	NA	NA
WP_099015954.1\|9066785_9067745_+	ABC transporter ATP-binding protein	A0A2H4PQG7	Staphylococcus_phage	1.5e-27	34.0
WP_099015955.1\|9067741_9068503_+	ABC transporter permease subunit	NA	NA	NA	NA
WP_099015956.1\|9069895_9070453_-	DoxX family protein	NA	NA	NA	NA
WP_099015957.1\|9070544_9071927_-	MFS transporter	A0A0M3UL24	Mycobacterium_phage	4.2e-31	36.9
WP_099015958.1\|9072040_9072544_-	metallophosphoesterase	NA	NA	NA	NA
WP_099017239.1\|9072644_9073211_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_099015959.1\|9073283_9076790_-	multidrug transporter	NA	NA	NA	NA
WP_099017240.1\|9076949_9077372_-	hypothetical protein	NA	NA	NA	NA
WP_099015960.1\|9077621_9078629_-	NAD(P)-dependent alcohol dehydrogenase	NA	NA	NA	NA
WP_167460055.1\|9078667_9079948_-	MFS transporter	NA	NA	NA	NA
WP_099015962.1\|9080086_9081520_-	mannitol dehydrogenase family protein	H8ZJP8	Ostreococcus_tauri_virus	5.0e-35	30.7
WP_099015963.1\|9081516_9082734_-	D-galactonate dehydratase family protein	Q6A202	Oenococcus_phage	1.3e-44	27.5
WP_099015964.1\|9082841_9083600_+	GntR family transcriptional regulator	NA	NA	NA	NA
WP_069860821.1\|9083718_9084243_-	discoidin domain-containing protein	NA	NA	NA	NA
WP_099015965.1\|9084920_9085481_-\|tail	phage tail protein I	NA	NA	NA	NA
WP_069860618.1\|9085482_9087471_-\|plate	putative baseplate assembly protein	NA	NA	NA	NA
9087090:9087109	attR	NA	NA	NA	NA
WP_020866084.1\|9087467_9087875_-	GPW/gp25 family protein	NA	NA	NA	NA
WP_069860619.1\|9087877_9088153_-	PaaR repeat-containing protein	NA	NA	NA	NA
WP_099015966.1\|9088275_9090195_-	VgrG-related protein	NA	NA	NA	NA
WP_069860621.1\|9090198_9091002_-	peptidase M23	NA	NA	NA	NA
WP_069860622.1\|9091005_9091437_-\|tail	phage tail protein	NA	NA	NA	NA
WP_099015967.1\|9091462_9093157_-	hypothetical protein	NA	NA	NA	NA
WP_087684351.1\|9093163_9093307_-	hypothetical protein	NA	NA	NA	NA
WP_069860625.1\|9093303_9093735_-	hypothetical protein	NA	NA	NA	NA
WP_069860626.1\|9093734_9094178_-\|tail	phage tail protein	NA	NA	NA	NA

DBSCAN-SWA_4

9196573 : 9264297

Bacillus_phage(25.0%)

plate,tail,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_099016016.1\|9196573_9197086_-\|protease	hydrogenase maturation protease	NA	NA	NA	NA
WP_099016017.1\|9197082_9198435_-	Ni/Fe hydrogenase subunit alpha	NA	NA	NA	NA
WP_069860693.1\|9198431_9199274_-	oxidoreductase	NA	NA	NA	NA
WP_099016018.1\|9199275_9200088_-	FAD/NAD(P)-binding protein	NA	NA	NA	NA
WP_079260162.1\|9200084_9200540_-	cyclic nucleotide-binding domain-containing protein	NA	NA	NA	NA
WP_093700649.1\|9200536_9201694_-	4Fe-4S dicluster domain-containing protein	NA	NA	NA	NA
WP_099016019.1\|9201899_9202613_-	SDR family oxidoreductase	A0A0M4JSW6	Mollivirus	7.0e-06	37.5
WP_069860698.1\|9202785_9203394_+	TetR family transcriptional regulator	NA	NA	NA	NA
WP_093701714.1\|9203514_9204306_-	FadR family transcriptional regulator	NA	NA	NA	NA
WP_099016020.1\|9204437_9206060_+	NAD(P)/FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_099016021.1\|9206049_9207273_-	peptidoglycan DD-metalloendopeptidase family protein	A0A1J0GVU2	Streptomyces_phage	6.8e-33	44.6
WP_099016022.1\|9207663_9208629_-	L-histidine N(alpha)-methyltransferase	NA	NA	NA	NA
WP_079260168.1\|9208625_9209381_-	ergothioneine biosynthesis protein EgtC	NA	NA	NA	NA
WP_099016023.1\|9209380_9210709_-	ergothioneine biosynthesis protein EgtB	NA	NA	NA	NA
WP_069860704.1\|9210705_9211971_-	ergothioneine biosynthesis glutamate--cysteine ligase EgtA	NA	NA	NA	NA
WP_069860705.1\|9212214_9213219_+	NADPH:quinone oxidoreductase family protein	NA	NA	NA	NA
WP_099017247.1\|9213242_9214421_+	acyl-CoA dehydrogenase	NA	NA	NA	NA
WP_099016024.1\|9214417_9215557_+	acyl-CoA/acyl-ACP dehydrogenase	NA	NA	NA	NA
WP_069860708.1\|9215849_9216044_+	hypothetical protein	NA	NA	NA	NA
WP_099016025.1\|9216103_9217492_-	cyclic nucleotide-binding domain-containing protein	A0A2K9L690	Tupanvirus	4.7e-22	31.6
WP_099016026.1\|9217563_9218976_-	cyclic nucleotide-binding domain-containing protein	A0A2K9L690	Tupanvirus	8.7e-24	31.5
WP_099016027.1\|9219374_9220280_+	hypothetical protein	NA	NA	NA	NA
WP_093706743.1\|9220408_9220897_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_099016028.1\|9220877_9222143_-	ROK family transcriptional regulator	NA	NA	NA	NA
WP_099016029.1\|9222273_9223731_-	xylulokinase	NA	NA	NA	NA
WP_069860714.1\|9223848_9225021_+	xylose isomerase	NA	NA	NA	NA
WP_099016030.1\|9225193_9226294_-	pectin esterase	NA	NA	NA	NA
WP_099017248.1\|9226785_9228027_-	SWF or SNF family helicase	NA	NA	NA	NA
WP_099016031.1\|9228155_9231077_-	DEAD/DEAH box helicase	D4P754	Rhodococcus_phage	9.5e-41	31.6
WP_069860718.1\|9231219_9231402_+	hypothetical protein	NA	NA	NA	NA
WP_099016032.1\|9231723_9232521_-	hypothetical protein	NA	NA	NA	NA
WP_099017249.1\|9233095_9233704_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_093701101.1\|9233986_9234505_+	roadblock/LC7 domain-containing protein	NA	NA	NA	NA
WP_099016033.1\|9234473_9235667_+	alcohol dehydrogenase catalytic domain-containing protein	NA	NA	NA	NA
WP_069860721.1\|9235720_9236149_-	PPOX class F420-dependent oxidoreductase	NA	NA	NA	NA
WP_069860722.1\|9236268_9236673_+	roadblock/LC7 domain-containing protein	NA	NA	NA	NA
WP_099016034.1\|9236771_9237752_+	hypothetical protein	NA	NA	NA	NA
WP_069860724.1\|9237780_9238671_-	acyl-CoA thioesterase II	NA	NA	NA	NA
WP_099016035.1\|9238732_9241261_-	DEAD/DEAH box helicase	M1I6E2	Acanthocystis_turfacea_Chlorella_virus	1.1e-45	34.0
WP_069860726.1\|9241397_9242189_+	metal-dependent hydrolase	NA	NA	NA	NA
WP_099016036.1\|9242233_9244015_-	ABC transporter ATP-binding protein	F2Y1V6	Organic_Lake_phycodnavirus	8.7e-05	23.5
WP_099016037.1\|9244011_9245949_-	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	2.7e-07	20.5
WP_099016038.1\|9246136_9246841_+	hypothetical protein	NA	NA	NA	NA
WP_069860729.1\|9246939_9247380_-	MarR family transcriptional regulator	NA	NA	NA	NA
WP_099016039.1\|9247515_9249459_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	1.6e-39	24.2
WP_079260189.1\|9249537_9250350_-	transcriptional regulator	NA	NA	NA	NA
WP_093701964.1\|9250525_9250753_-	hypothetical protein	NA	NA	NA	NA
WP_069860733.1\|9250931_9251510_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_099016040.1\|9251506_9252232_+	carboxypeptidase regulatory-like domain-containing protein	NA	NA	NA	NA
WP_099016041.1\|9252242_9254507_+\|tail	phage tail protein	J9PVC2	Bacillus_phage	9.0e-47	31.4
WP_069860736.1\|9254526_9254982_+\|tail	phage tail protein	NA	NA	NA	NA
WP_099016042.1\|9254983_9256477_+\|tail	phage tail protein	H6WFT7	Cyanophage	5.4e-16	31.8
WP_069860738.1\|9256473_9256992_+\|tail	phage tail protein	T2KT02	uncultured_phage	1.4e-08	37.8
WP_093701969.1\|9256988_9257183_+	hypothetical protein	NA	NA	NA	NA
WP_069860740.1\|9257295_9257967_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_069860741.1\|9257977_9259159_+	phage late control D family protein	NA	NA	NA	NA
WP_079260195.1\|9259155_9259857_+	type IV secretion protein Rhs	NA	NA	NA	NA
WP_069860743.1\|9259853_9260267_+	GPW/gp25 family protein	NA	NA	NA	NA
WP_099016043.1\|9260263_9262213_+	hypothetical protein	NA	NA	NA	NA
WP_099016044.1\|9262209_9264297_+\|plate	putative baseplate assembly protein	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP023992

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection