CRISPRimmunity

Please click to download your results

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_CP030771	Streptomyces sp. YIM 121038 chromosome, complete genome	18 crisprs	csa3,WYL,casR,DEDDh,cas4,Cas9_archaeal,cas3,PD-DExK,DinG	2	6	7	0
NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	0 crisprs	DEDDh,RT,c2c9_V-U4,csa3	0	0	6	0

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP030771_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_1

255941-256046

Orphan

Consensus_repeat	Method
GGCGGTGCGGCGACTGAAGGTGGTACTGCGATCG	CRISPRCasFinder

1 spacers

csa3

The CRISPR arrays of NZ_CP030771_1

>merge|NZ_CP030771|1|255941-256046|CRISPRCasFinder
GGTGGTGGTGCGACCGAGGGCGGTGCGGCGACTGAAGGTGGTACTGCGATCGAAGGCGGTGCGACGACTGAAGGTGGTACTGCGATCGAAGGCGGTGCGACGACTG

>NZ_CP030771|1|1|255941-256046|CRISPRCasFinder
GGTGGTGGTGCGACCGAGGGCGGTGCGGCGACTG	AAGGTGGTACTGCGATCGAAGGCGGTGCGACGACTGAA
GGTGGTACTGCGATCGAAGGCGGTGCGACGACTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138957444.1\|269390_269924_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379112
NZ_CP030771.1\|WP_138957442.1\|263509_264112_+\|flavin-reductase	unknown	unknown	gnl\|CDD\|214900
NZ_CP030771.1\|WP_138957437.1\|254912_255863_-\|agmatinase	unknown	unknown	gnl\|CDD\|212538
NZ_CP030771.1\|WP_138957428.1\|245391_245832_+\|anti-sigma-factor-antagonist	unknown	unknown	gnl\|CDD\|132914
NZ_CP030771.1\|WP_138957440.1\|259729_262054_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|276938
NZ_CP030771.1\|WP_171075592.1\|268316_269183_-\|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl\|CDD\|366736
NZ_CP030771.1\|WP_138957441.1\|262323_263487_+\|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ	unknown	unknown	gnl\|CDD\|239065
NZ_CP030771.1\|WP_138957434.1\|251596_252604_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381302
NZ_CP030771.1\|WP_138957435.1\|252646_253786_+\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|224871
NZ_CP030771.1\|WP_138957431.1\|248448_248754_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	unknown	unknown	gnl\|CDD\|238042
NZ_CP030771.1\|WP_138957429.1\|246089_246440_+\|metalloregulator-ArsR/SmtB-family-transcription-factor	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|197713
NZ_CP030771.1\|WP_138957433.1\|250935_251580_+\|nitroreductase-family-protein	unknown	unknown	gnl\|CDD\|380311
NZ_CP030771.1\|WP_138957445.1\|270378_271203_-\|AraC-family-ligand-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|225117
NZ_CP030771.1\|WP_138957443.1\|264095_267074_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276938
NZ_CP030771.1\|WP_138957438.1\|256073_257618_-\|asparagine-synthetase-B	unknown	unknown	gnl\|CDD\|223444
NZ_CP030771.1\|WP_138957439.1\|257621_259337_-\|thiamine-pyrophosphate-binding-protein	unknown	unknown	gnl\|CDD\|223107
NZ_CP030771.1\|WP_138957430.1\|247530_248157_+\|DUF308-domain-containing-protein	unknown	unknown	gnl\|CDD\|225786
NZ_CP030771.1\|WP_171075591.1\|267350_268145_+\|DeoR/GlpR-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224268
NZ_CP030771.1\|WP_138957436.1\|253941_254916_-\|TauD/TfdA-family-dioxygenase	unknown	unknown	gnl\|CDD\|238154
NZ_CP030771.1\|WP_138957432.1\|249477_250851_+\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|223239

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138957444.1\|269390_269924_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.73797e-30
NZ_CP030771.1\|WP_138957442.1\|263509_264112_+\|flavin-reductase	gnl\|CDD\|214900	smart00903, Flavin_Reduct, Flavin reductase like domain. This entry represents the FMN-binding domain found in NAD(P)H-flavin oxidoreductases (flavin reductases), a class of enzymes capable of producing reduced flavin for bacterial bioluminescence and other biological processes. This domain is also found in various other oxidoreductase and monooxygenase enzymes... This domain consists of a beta-barrel with Greek key topology, and is related to the ferredoxin reductase-like FAD-binding domain. The flavin reductases have a different dimerisation mode than that found in the PNP oxidase-like family, which also carries an FMN-binding domain with a similar topology.	1.23164e-44
NZ_CP030771.1\|WP_138957437.1\|254912_255863_-\|agmatinase	gnl\|CDD\|212538	cd11592, Agmatinase_PAH, Agmatinase-like family includes proclavaminic acid amidinohydrolase. This agmatinase subfamily contains bacterial and fungal/metazoan enzymes, including proclavaminic acid amidinohydrolase (PAH, EC 3.5.3.22) and Pseudomonas aeruginosa guanidinobutyrase (GbuA) and guanidinopropionase (GpuA). PAH hydrolyzes amidinoproclavaminate to yield proclavaminate and urea in clavulanic acid biosynthesis. Clavulanic acid is an effective inhibitor of beta-lactamases and is used in combination with amoxicillin to prevent the beta-lactam rings of the antibiotic from hydrolysis and, thus keeping the antibiotic biologically active. GbuA hydrolyzes 4-guanidinobutyrate (4-GB) into 4-aminobutyrate and urea while GpuA hydrolyzes 3-guanidinopropionate (3-GP) into beta-alanine and urea. Mutation studies show that significant variations in two active site loops in these two enzymes may be important for substrate specificity. This subfamily belongs to the ureohydrolase superfamily, which includes arginase, agmatinase, proclavaminate amidinohydrolase, and formiminoglutamase.	1.76975e-137
NZ_CP030771.1\|WP_138957428.1\|245391_245832_+\|anti-sigma-factor-antagonist	gnl\|CDD\|132914	cd07043, STAS_anti-anti-sigma_factors, Sulphate Transporter and Anti-Sigma factor antagonist) domain of anti-anti-sigma factors, key regulators of anti-sigma factors by phosphorylation. Anti-anti-sigma factors play an important role in the regulation of several sigma factors and their corresponding anti-sigma factors. Upon dephosphorylation they bind the anti-sigma factor and induce the release of the sigma factor from the anti-sigma factor. In a feedback mechanism the anti-anti-sigma factor can be inactivated via phosphorylation by the anti-sigma factor. Well studied examples from Bacillus subtilis are SpoIIAA (regulating sigmaF and sigmaC which play an important role in sporulation) and RsbV (regulating sigmaB involved in the general stress response). The STAS domain is also found in the C- terminal region of sulphate transporters and stressosomes.	4.47975e-08
NZ_CP030771.1\|WP_138957440.1\|259729_262054_+\|AAA-family-ATPase	gnl\|CDD\|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	5.65796e-34
NZ_CP030771.1\|WP_171075592.1\|268316_269183_-\|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.	2.76054e-09
NZ_CP030771.1\|WP_138957441.1\|262323_263487_+\|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ	gnl\|CDD\|239065	cd02152, OAT, Ornithine acetyltransferase (OAT) family; also referred to as ArgJ. OAT catalyzes the first and fifth steps in arginine biosynthesis, coupling acetylation of glutamate with deacetylation of N-acetylornithine, which allows recycling of the acetyl group in the arginine biosynthetic pathway. Members of this family may experience feedback inhibition by L-arginine. The active enzyme is a heterotetramer of two alpha and two beta chains, where the alpha and beta chains are the result of autocatalytic cleavage. OATs found in the clavulanic acid biosynthesis gene cluster catalyze the fifth step only, and may utilize acetyl acceptors other than glutamate.	0
NZ_CP030771.1\|WP_138957434.1\|251596_252604_+\|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.	6.45655e-142
NZ_CP030771.1\|WP_138957435.1\|252646_253786_+\|acyl-CoA-dehydrogenase	gnl\|CDD\|224871	COG1960, CaiA, Acyl-CoA dehydrogenases [Lipid metabolism].	1.24501e-23
NZ_CP030771.1\|WP_138957431.1\|248448_248754_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	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.	2.87845e-07
NZ_CP030771.1\|WP_138957429.1\|246089_246440_+\|metalloregulator-ArsR/SmtB-family-transcription-factor	gnl\|CDD\|197713	smart00418, HTH_ARSR, helix_turn_helix, Arsenical Resistance Operon Repressor.	3.10071e-15
NZ_CP030771.1\|WP_138957433.1\|250935_251580_+\|nitroreductase-family-protein	gnl\|CDD\|380311	cd02062, Nitro_FMN_reductase, nitroreductase family protein. Proteins of this family catalyze the reduction of flavin or nitrocompounds using NAD(P)H as electron donor in a obligatory two-electron transfer, utilizing FMN or FAD as cofactor. They are often found to be homodimers. Enzymes of this family are described as NAD(P)H:FMN oxidoreductases, oxygen-insensitive nitroreductase, flavin reductase P, dihydropteridine reductase, NADH oxidase or NADH dehydrogenase.	1.76437e-24
NZ_CP030771.1\|WP_138957445.1\|270378_271203_-\|AraC-family-ligand-binding-domain-containing-protein	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.4384e-23
NZ_CP030771.1\|WP_138957443.1\|264095_267074_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	2.61215e-27
NZ_CP030771.1\|WP_138957438.1\|256073_257618_-\|asparagine-synthetase-B	gnl\|CDD\|223444	COG0367, AsnB, Asparagine synthase (glutamine-hydrolyzing) [Amino acid transport and metabolism].	2.73827e-48
NZ_CP030771.1\|WP_138957439.1\|257621_259337_-\|thiamine-pyrophosphate-binding-protein	gnl\|CDD\|223107	COG0028, IlvB, Thiamine pyrophosphate-requiring enzymes [acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase] [Amino acid transport and metabolism / Coenzyme metabolism].	1.89784e-122
NZ_CP030771.1\|WP_138957430.1\|247530_248157_+\|DUF308-domain-containing-protein	gnl\|CDD\|225786	COG3247, HdeD, Uncharacterized conserved protein [Function unknown].	2.03584e-15
NZ_CP030771.1\|WP_171075591.1\|267350_268145_+\|DeoR/GlpR-transcriptional-regulator	gnl\|CDD\|224268	COG1349, GlpR, Transcriptional regulators of sugar metabolism [Transcription / Carbohydrate transport and metabolism].	5.1611e-69
NZ_CP030771.1\|WP_138957436.1\|253941_254916_-\|TauD/TfdA-family-dioxygenase	gnl\|CDD\|238154	cd00250, CAS_like, Clavaminic acid synthetase (CAS) -like; CAS is a trifunctional Fe(II)/ 2-oxoglutarate (2OG) oxygenase carrying out three reactions in the biosynthesis of clavulanic acid, an inhibitor of class A serine beta-lactamases. In general, Fe(II)-2OG oxygenases catalyze a hydroxylation reaction, which leads to the incorporation of an oxygen atom from dioxygen into a hydroxyl group and conversion of 2OG to succinate and CO2.	6.65218e-38
NZ_CP030771.1\|WP_138957432.1\|249477_250851_+\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|223239	COG0161, BioA, Adenosylmethionine-8-amino-7-oxononanoate aminotransferase [Coenzyme metabolism].	1.17887e-154

>NZ_CP030771.1|WP_138957437.1|254912_255863_-|agmatinase
MDRIDTTVSPRYAQIPTFMRLPHDPAPHGKDVVVIGAPYDGGTSYRPGARFGPRAVRGESGLIHGVGIDRGPGTFDLIDCVDAGDIDLTPFNMHIAMATAQERLSGLLADNAAFLMIGGDHSLTLAALRAVAARHGPVAVLHLDAHSDTNPAVYGGEYHHGTPFRHAIEEKLVDPLRMVQIGIRGHNPRPDSLDYARGHGVRIVTSDEFCALGPEDAGRLVRSLLGDAPVYVSVDVDVVDPAFAPGTGTPAPGGPTSREVLALLRHVGALRPVGFDVMEVSPPYDHGGVTSLLASEIGAELLFQYARAHTRERTSP
>NZ_CP030771.1|WP_138957436.1|253941_254916_-|TauD/TfdA-family-dioxygenase
MTELDCSPYSARLLELAARLPRVPRRDLHGFLAAARTAADALPAPLAGTLDDFRADGNRNGYLLLRGLPVEEDDALPRTPDSTPAPVDRPLLNQEAMLAIVGRRLGLHTGYRELRSATVYHDVYPSPGAHYLSSETSETLLEFHTEMAYHVRQPNYVLLACSRADHERTAATLVGSVRKALPLLPDAVRDRLFDRPLPCCVDVAFRGGADDPGALANVKPLYGDPRDPFLGYDRELLAPRDAADIEAVTVLSKALDEVREAVYLIPGDLLVVDNFRTTHARTPFVPRWDGKDRWLHRVYIRTERNGQLSGGERAGDVVDFVPRR
>NZ_CP030771.1|WP_138957435.1|252646_253786_+|acyl-CoA-dehydrogenase
MRFLQLDHEVCEELLPGLAGRLADVPFDELESPASPAIALFKEYGGTNLLVPRDYGGIGASALDAVRVIRALASLAPSLAVATAMHHFSVGMLFAVGPLYESGTGIHTSVLDVVAKNRSLIASGYAEGRSGRGILTPTVEARETAGGYLVSGSKKPCSLSRSMDFLTASVALPGDDGDAGMGLLVLPSDTPGISVHEFWSTFPLAGAESHEVRLTDVFARAEHVLRAPANAAEKLDELNEAGVIWFQMIVAASYTGVASALVDLVLRERRGSAGERARLCLLIESAASLVEGVARRIMDGDLGNDCAAASLFTRFSVQDVITRAVSQAVEMLGGMAFVTSPRIACLASAAQAVVFHPPSRMSMSEAVVDYYAGKPLLFS
>NZ_CP030771.1|WP_138957434.1|251596_252604_+|aldo/keto-reductase
MRHDDGSPLPTRALGGLTLPAQGLGCLSMTSFYASAEPAEAVATVRHAIDRGVTLLDTADVQGLGEGERLLGKAVAGRRDRVLISTKVGLERDRDGMFLGVRGDRAYIRERCHASLRRLGVDHLDFYVKHWAAPGERVEEAVGALAELVTEGKVRHLCLSEVSADTIRRAHAVHPVTAVQSEWSLVSRGIEAQVLPVCRELGIGVIASCPLGRGLLTGRIASVADLGPAADFRRTLPRFEPLHLARNQAVVDALRPLAASRDLSVAQLALAWLHHQGDDVVPIPGTGRRGHLAENLGAAFVGLTAEELRTVESAVSAAGVHGERYPPFLMRLVDN
>NZ_CP030771.1|WP_138957433.1|250935_251580_+|nitroreductase-family-protein
MTPLDLTPDELLTTTRSVRKRLDLTRPVPLELVEDCVRVALQAPTGSNRQSWHWMVVTDARQRALIGGYYRRAVREYLRSEGTCASLFPEDPARHAVQRRVGDSVAHLGEHMAEVPVHVIPCLDVNDAPEYNEAGKWGSIVQAAWSYMLAARARRLGTAWTTLHLMYEKEIAELLGLPDGVVQAALIPTAFSLGTRFRPAARQPLERVLHVDTW
>NZ_CP030771.1|WP_138957432.1|249477_250851_+|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme
MSTSSVARIPGSDRTARWVRADRDRLIHPNLPSGLTERTVMVEGQGCYVRDSSGRRYLDAAAVLGMMQVGHGRGEIVRAAAAQMGTLECFHLWESMSNDKAIELAVRLGDLAPTGLDRVFFTSGGAEGNEIALRMARFFHHRRGEPERTWILSRRTAYHGIAYGAGSVSGLPVYHEGFGPSLPHVHHLTAPDPYQGVGYEGEDVTEFCLRELRETIERIGPDRIAAMIGEPVMSVGGAVVPPPDYWPRVAELLDAHGILLIFDEVVTAYGRTGHWFAAEHFGVRPDLLVTAKGITSGYVPHGAVLVTEEVASAVTAANGFPIGFTYTGHPTACAVALTNLDLIEREKLLDNATVTGGHLADRLAALSELPVVGEVRQIGLMLGIELVADKRTRTQLPTGTAPVARALREDAGIILRGNPRSLLINPPLVLNRAEADELADGLHAVLARVDPDGRVRP
>NZ_CP030771.1|WP_138957431.1|248448_248754_-|metalloregulator-ArsR/SmtB-family-transcription-factor
MPNSLYEAQAELLQVLGHPVRIRVLEVLQGGPVPVRELLAALGLEIELPELSQHLAGLLGCGVVVVNRRGATAVYEVVGGDVAELLAVARRVSAVRLLGAW
>NZ_CP030771.1|WP_138957430.1|247530_248157_+|DUF308-domain-containing-protein
MGDMEHIGEVGRPHRGGAGNPLERLGKVAWQALMLLGFAAIAIGVVALVWPGRTLLVLGVLFGIYLLISGVMEIVAAFGAFVSAGMRVLLVVTGALSITLGVLCFRNSLHNSVLLLSLWIGIGFLMYGIATAVTAAEMHSGWGVSLGLLAAAGGIIVLSWPIGSIVTLAVFTGIWLIAVGLTEVIHAFTLRSLVRSAGGSRRHATAVA
>NZ_CP030771.1|WP_138957429.1|246089_246440_+|metalloregulator-ArsR/SmtB-family-transcription-factor
MSRPLYQLKAEFFKTLGHPVRIRVLELLSVREHAVAEMLPEVGVEPAHLSQQLAVLRRANLVVTRKEGSTVYYSLTSPHVAELLKVARTILSGVLASQAGLLADLQTAAAETEPPS
>NZ_CP030771.1|WP_138957428.1|245391_245832_+|anti-sigma-factor-antagonist
MTIEWRYTVEPDLGILSVAGHLGQDAARRFTGAVGWVLARGTGPVIVDCTELRGWSVQGQLALAEAARRLAEHGRRLELAAIPADGSLVPVGDCPPVPVHCDLTTALAAHRTQRQAATGRPEEQRQAATGGPEEQRQEWRTGGWSG
>NZ_CP030771.1|WP_138957438.1|256073_257618_-|asparagine-synthetase-B
MEATLPAATGFQAEVRLDGGGPLAPDFASRGSLARWHERTADRVLHAVLLHSGAPDRACAHHQDRTLVFAGELYNQGELLGLLPGRALPDGDAALILALFDVYGAPVFRLLNGRFAALFTDSRRAVLATDHAGSVPLYVSVAPGRVLAATEAKALRAAPRGRPAPARPVRGRLGIHQVPAGTALDIEVATGKCVTHRTWAPPSARRILPEDEAADAVRRTLERAVAARTGAGTPLVVLSGGIDSSSVAALAARRSPGPIDTVSMGTDEADEFPQARVVARHIGSAHQEITVPTPELLRQLPYAVWAAECLDPDVVEYLLPLTALYLRLGGTGADGAAGRRVLTGYGADIPLGGMHREGRLPHLEEAVCRDMNTFDGLNEMTPTLSAVAGHWSTHPYWDRDVLDLLVSVEAGLKHRHGRDKWVLRAAMRGVLPHEVLVRPKLGVHEGSGTTSSFTRLLQDAGVPQDRVRQAKRLVVREIFDQVVVGGRHPDEVAVDAIARLVADREPRGARPAPR
>NZ_CP030771.1|WP_138957439.1|257621_259337_-|thiamine-pyrophosphate-binding-protein
MSRVSTGPRTTQTTAHALLRRLHDHGVRTVFGVVGREAASILFDEADGVDFVLTRHEFTAGVAADVLARITGRPQACWATLGPGMTNLATGVATSVLDRSPVVALAAQSESHDIFPNDTHQCLDSVSVMGPLTKYCVELRRPDDITDLVDSAVSAAMTEPVGPSFISLPVDLLGSEVDTARPHPGARVLAKPVGAVEDGWRGSALRVAELIGAARHPVLVVGAAAIRSGAVPAVRALAERLRTPVITTYTAKGVLPHGHELDYGAVTGYMDGILDFPALDTLFGPADLVLTLGYDYAEDLRPSMWQRGADKTTVRVSPTANPVPRVYRPDLDVVTDVREFVELLDQRTAGLAAKTPHDVSPLRERVAEFLADPRQYDDGLRVHQVMDSMNTVMAESAEAGEGTIVSDIGFFRHYGVLFARADQPYGFLTSAGCSSFGYGIPAAIGAQLARPGQPTFLIAGDGGFHSNSADLETIARLNLPIVTVVVNNDANGLIELYQNIGHHRSHGPAVRFTGVDFTTLARANGVEAVRATTREELLAALRKGVGLGRPFLVEVPVNYDFRAGGFAALTI
>NZ_CP030771.1|WP_138957440.1|259729_262054_+|AAA-family-ATPase
MDHAAVSPHVPSAPGEPAARRSTRPRDRRGTQPRGEARSPPVRTPFRRNGAGRRARQRGPDDVKPTSCEPRAGLRDLTGAPPIGTLGCLSVHVHGRPLELGPPRQRAVLALLLISAGSVVSVDSIITQIWGDTPPAAAHATLQSYVSRLRKLLADCVLPDGSRPRLHYRQPGYALAIDPEHVDVHSFERIARAGVRLAQKGRAEEAHALLGTILDDWHGAPYDELNAYDFAVHEAARLEQLRLSALEAWAQCALGLGGEEDALHTLAQEARRNPLRERLIGLYMHAQYRLGRQADALHTYERTRRALADEIGADPGKELAALHAAILRQDGCLDRAPGTTAAAVGGHSSAAAVAPRSPAATEPGRIMIPPPRLRPGRGRDAGARPRGCGGTRPVFVGRDEEVRALSESATGAFHSSGRVAFVVGEAGSGKTRLVSELAGTVPHGVHVVWGSCSESEDKPDYWPWTTLLRRLNRLWPERVRRLPGWVRHSVARLLPELASDGCDLPHPRPGPGPGPEPLTRDARFTLHDAVCQTLLCTVREPTILVVEDVDRADAPSLAVLRLLVEQVRTVPVLLVVTSRTFQLAHDGALRRAAAVILQSPDARRIPLKPLDLPATRSLVESTLGEIPEPHLLDRLHRRTAGNPFFLGYLLHARRQGLSAGPDAAIPHELAGVVLQRLSGLPPGVRRALELCAVSEEGCAPRVVEAVLRREGIPADVLLMAVHGGLLEFASAGADRLRFVHPLVREAVRYDVENARAVASTADGVADAARRPGAR
>NZ_CP030771.1|WP_138957441.1|262323_263487_+|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ
MHASSPQGFRVHHGRVGIKEAGPDFAVIASEVPATVSAVFTRSRFAGPSVLISREAVADRSARGVVVLSGNANVATGAEGHQDAEEVRRRVAASIGADENDVLIASTGLIGHPYPMPRVRSHLASLRWPFPGADFDAAATAIMTTDTRPKVRRARCGDATLVGIAKGVGMMEPDMATLLTFFCTDARVGPVVLDDVFRRVMDRTFNALSIDTDTSTSDTGAILANGLAGPVDLVAFEEALDAVALGLVKDIARDGEGATKLIEVRVTGARDTGQAKRVAKAVVNSPLVKTAVHGADPNWGRVAMAVGKCQDDLDIVPERVTIGFGDQEVYPGRPGPEQLAHVAERLKGDEVVLRVDLGVGGHSPGEFTAYGCDLTEGYVRLNADYST
>NZ_CP030771.1|WP_138957442.1|263509_264112_+|flavin-reductase
MTYDSDRLAGSEGGARQTDFRTILGRYPTGVALVTAPAGGPGADPLGMVVGTFTSVSLDPPLVGFLPARTSTTWPGIRAAGRFCVNVLGAGQRDVCEAFATRSPHRWEVSHRGSPSGCPVLPDAVAWIDCAVHAQTEAGDHWFVTGLVRAMGVGGQGPPMVFLGGRYGSYAPRPPRWDQALGPVQGPAPALRARRLRRDP
>NZ_CP030771.1|WP_138957443.1|264095_267074_-|tetratricopeptide-repeat-protein
MRFTVLGPVRAWHGRTEVTPSPPKQRALLALLLVRAGSPVGLSDVIDVLWPQGPPRSAPNVVRHHVSALRRLLSAEGNGGGAVPLTRGCGGYRLDVDADCLDLLVFRQLAERARQATRDGSPPTATGLYADALALWQGPAACGIAAEVRTHPVFAAVDEECVSTVRAAAAVALAAGASDRVLAPLRQAAAAHPLDESVQAHLVLALSATGRQAEALAAYRAVRERLAEELGVGPGRELTDAQQRVLGQHPAAARRARPQPEATARPAPDTYTGDPPPPPRTPSAVTRPSRTPSAVTPPAPRSPSTAAPSPPRTPRVRPAHLPADLPVFAGRDDDLARAEALSTRRGSHGATASPAPTITVIEGMAGVGKTSLAVHWAHGVASRFPDGQLYADLRGFDPAGAALESGEILRAFLHGLGVHPQDMPVGLDARAALYRHLLADRRVLVLLDNARDSAQVRPLLPGAPGCHVMVTSRNRLQGLIAAEGARSIVLGPLSEAEGREVLSRRLGAQRIAAEAAAAEAIIALCGRLPLALAIVAARAGSGPGFPLASVAAELREGHGGLDAFSGDEADVRAVFSWSHRYLTPTTARLFRLLSLHPGPEVSRHAAASLAGLGPREARAALADLTRSHLLTEPAPGRYACHDLLRAYAGERVRAEETEHGRRDALGRLLDHALHTAQTAVDLLYPHRTEREPPPSRHTGATPAPLCGRESAAAWLTVELPALLALVESADTGGFLTHAWQLALALELFADRRGLRDEQISLQRAGLAAAERLGDPLGRAHLHRTLGFALHRTGADAEARSHLDRALRLFTALDHRDGQARTLRSLAFLANSRARHEEALEHYARALAHYRTTADVRGQANVLNEIGWTHILRGDHHEALTRCATAVALHQDTGDAGGEAAAWDSIGYAHHHLGQYTHALSCYRQALVLYREIGERTLEAESIGHVGDTLHAQGDHRAARASWEHAAAILAEWGHPDADRLLEKLHDATTGPA
>NZ_CP030771.1|WP_171075591.1|267350_268145_+|DeoR/GlpR-transcriptional-regulator
MTGTATGRVSVTEGEERRRHIVVTARRAGSVDVTAIAADLGVSKETVRRDLSWLARRGLLRRTHGGAYPLQSTGFETTLASRTRTHVEEKTRIAAAAAGLLRDAGTVFVDEGHTPQLVAEALPDDRPLTVITASLAAAQALATRPRARVLLLGGRVRSGTMATVDHWAARMLSEFAVDLAYLSANGISREHGLTTPDPTVSEVKRQAVRVSRRRVFCGVHAKFGAVSLCRFAEARAFETIVTDIRLPQSEARRYALLGPEVLRV
>NZ_CP030771.1|WP_171075592.1|268316_269183_-|aminoglycoside-phosphotransferase-family-protein
MEMSDVTRATAAATSIAASLGLPASGAIVLHNSNKLALRLTPCDVFARVAPVGQEVAQFEVELAQRLTGTGCPVCPLEPRAAPRVYTRDGFTVTLWTYYEPVTPHVSPADCAKALELLHAGMRKVDVPSPRFTDRITEAEEVVADPERSPELADADRVFLSGRLASLRRAIEERGAAEQLLHGEPHPGNVLSTETGPLFIDLETCCRGPVEFDLAHVPEEVCEHYPDIDQGLLDECRQLVLAMVAAWRWELGDQFPKGRLFGEELLRALHEGPPWPTLDTMSKRLGGL
>NZ_CP030771.1|WP_138957444.1|269390_269924_-|GNAT-family-N-acetyltransferase
MTEIRTPRLLLRRWHDDDLAPMADINADPRVMRWIDDGSVRDLDHTAEEIERWEEEWDEEGFGLFAVELLASGELAGFTGLSVPEFLPEAGPAVAISWRLGSPFWGQGYASEAAHATLEFALQDRGLDRVISISRVGDHASENIIRKLGMVPERETTHPQYAYPLQVHTIDLTEFQA
>NZ_CP030771.1|WP_138957445.1|270378_271203_-|AraC-family-ligand-binding-domain-containing-protein
MTSSAERAAYWRVPELALEAMDARFERYAYPMHAHDTYSFGVTDHGAQSFVCRGERHVSAAGLVMVFNPDDPHDGQSAVRDGYRYRMLHLGEDHVRDVLADALPTEARLPLFDTPVVDNPALARAVARLHAAVTENAPRLVVEERLTAAVLLLSRHASTKPTPGPDRPGRTDLAALDRARTLLRQRFADNISADDLARAAGCSRFTLYRGFRTAYGFAPSDYQRDLRLRRARALLAEGTPPATAAAEAGFADQAHLTRWFARTYGVTPAAYRTA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_2

673498-673708

Orphan

Consensus_repeat	Method
TCCAGGACGACGGCAACCTCGTCATCTACGACG	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP030771_2

>merge|NZ_CP030771|2|673498-673708|PILER-CR
TCCGACGGCAACCTCGTCATCTACGACGAGTTCAACCGGCCCAGATGGGCGAGCCGGACCGTCGGCCAGGGCTGGACCACGCGCTTCCAGGAGGACGGCAACCTCGTCGTCTACACCCGCAGCGGCCGCGCCGTCTGGGCGTCCCACACCGCGGGGCACCCCGGCTCCCGCCTCGTCATCCAGGACGACGGCAACGTCGTCATCTACGACG

>NZ_CP030771|2|1|673498-673708|PILER-CR
TCCGACGGCAACCTCGTCATCTACGACGAGTTC	AACCGGCCCAGATGGGCGAGCCGGACCGTCGGCCAGGGCTGGACCACGCGCTTCCAG
GAGGACGGCAACCTCGTCGTCTACACCCGCAGC	GGCCGCGCCGTCTGGGCGTCCCACACCGCGGGGCACCCCGGCTCCCGCCTCGTCATCCAGGACG
ACGGCAACGTCGTCATCTACGACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138957769.1\|681975_682383_+\|DUF3224-domain-containing-protein	unknown	unknown	gnl\|CDD\|371584
NZ_CP030771.1\|WP_138965939.1\|666905_667415_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226728
NZ_CP030771.1\|WP_138957757.1\|665672_666275_-\|carbonic-anhydrase	unknown	unknown	gnl\|CDD\|238449
NZ_CP030771.1\|WP_138957756.1\|664046_665627_-\|SulP-family-inorganic-anion-transporter	unknown	unknown	gnl\|CDD\|223732
NZ_CP030771.1\|WP_138957761.1\|670448_671645_-\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|173848
NZ_CP030771.1\|WP_138957765.1\|675980_677633_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|312032
NZ_CP030771.1\|WP_138965954.1\|672353_673028_+\|FCD-domain-containing-protein	unknown	unknown	gnl\|CDD\|225097
NZ_CP030771.1\|WP_138957759.1\|667509_668757_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224458
NZ_CP030771.1\|WP_138965956.1\|674049_674868_+\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138957772.1\|684482_685439_-\|MEDS-domain-containing-protein	unknown	unknown	gnl\|CDD\|379605
NZ_CP030771.1\|WP_138957766.1\|677759_678185_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|131480
NZ_CP030771.1\|WP_138957762.1\|671686_672169_-\|flavin-reductase	unknown	unknown	gnl\|CDD\|214900
NZ_CP030771.1\|WP_138957767.1\|678204_680400_-\|glycoside-hydrolase	unknown	unknown	gnl\|CDD\|236653
NZ_CP030771.1\|WP_138957760.1\|669360_670209_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379312
NZ_CP030771.1\|WP_138957770.1\|682486_683329_-\|DUF1206-domain-containing-protein	unknown	unknown	gnl\|CDD\|377695
NZ_CP030771.1\|WP_171075619.1\|668867_669020_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138957771.1\|683693_684431_+\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|214473
NZ_CP030771.1\|WP_138957758.1\|666343_666811_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237171
NZ_CP030771.1\|WP_138957764.1\|675085_675967_+\|universal-stress-protein	unknown	unknown	gnl\|CDD\|238182
NZ_CP030771.1\|WP_138957768.1\|680517_681834_-\|cytochrome-P450	unknown	unknown	gnl\|CDD\|365848

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138957769.1\|681975_682383_+\|DUF3224-domain-containing-protein	gnl\|CDD\|371584	pfam11528, DUF3224, Protein of unknown function (DUF3224). This bacterial family of proteins has no known function.	1.31056e-36
NZ_CP030771.1\|WP_138965939.1\|666905_667415_-\|hypothetical-protein	gnl\|CDD\|226728	COG4278, COG4278, Uncharacterized conserved protein [Function unknown].	4.47056e-06
NZ_CP030771.1\|WP_138957758.1\|666343_666811_-\|hypothetical-protein	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	0.000798491
NZ_CP030771.1\|WP_138957756.1\|664046_665627_-\|SulP-family-inorganic-anion-transporter	gnl\|CDD\|223732	COG0659, SUL1, Sulfate permease and related transporters (MFS superfamily) [Inorganic ion transport and metabolism].	1.3562e-89
NZ_CP030771.1\|WP_138957761.1\|670448_671645_-\|acyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|173848	cd01159, NcnH, Naphthocyclinone hydroxylase. Naphthocyclinone is an aromatic polyketide and an antibiotic, which is active against Gram-positive bacteria. Polyketides are secondary metabolites, which have important biological functions such as antitumor, immunosupressive or antibiotic activities. NcnH is a hydroxylase involved in the biosynthesis of naphthocyclinone and possibly other polyketides.	2.38033e-112
NZ_CP030771.1\|WP_138957765.1\|675980_677633_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|312032	pfam08386, Abhydrolase_4, TAP-like protein. This is a family of putative bacterial peptidases and hydrolases that bear similarity to a tripeptidyl aminopeptidase isolated from Streptomyces lividans. A member of this family is thought to be involved in the C-terminal processing of propionicin F, a bacteriocidin characterized from Propionibacterium freudenreichii.	1.83427e-21
NZ_CP030771.1\|WP_138965954.1\|672353_673028_+\|FCD-domain-containing-protein	gnl\|CDD\|225097	COG2186, FadR, Transcriptional regulators [Transcription].	1.36453e-17
NZ_CP030771.1\|WP_138957759.1\|667509_668757_-\|hypothetical-protein	gnl\|CDD\|224458	COG1541, PaaK, Coenzyme F390 synthetase [Coenzyme metabolism].	2.68043e-06
NZ_CP030771.1\|WP_138957772.1\|684482_685439_-\|MEDS-domain-containing-protein	gnl\|CDD\|379605	pfam14417, MEDS, MEDS: MEthanogen/methylotroph, DcmR Sensory domain. MEDS is prototyped by DcmR and is likely to function with the PocR domain in certain organisms in sensing hydrocarbon derivatives. The MEDS domain occurs fused to Histidine Kinase and as stand-alone version. Sequence analysis shows that it is a catalytically inactive version of the P-loop NTPase domain of the RecA superfamily.	1.42291e-30
NZ_CP030771.1\|WP_138957766.1\|677759_678185_-\|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].	2.80976e-08
NZ_CP030771.1\|WP_138957762.1\|671686_672169_-\|flavin-reductase	gnl\|CDD\|214900	smart00903, Flavin_Reduct, Flavin reductase like domain. This entry represents the FMN-binding domain found in NAD(P)H-flavin oxidoreductases (flavin reductases), a class of enzymes capable of producing reduced flavin for bacterial bioluminescence and other biological processes. This domain is also found in various other oxidoreductase and monooxygenase enzymes... This domain consists of a beta-barrel with Greek key topology, and is related to the ferredoxin reductase-like FAD-binding domain. The flavin reductases have a different dimerisation mode than that found in the PNP oxidase-like family, which also carries an FMN-binding domain with a similar topology.	7.73447e-46
NZ_CP030771.1\|WP_138957767.1\|678204_680400_-\|glycoside-hydrolase	gnl\|CDD\|236653	PRK10137, PRK10137, alpha-glucosidase; Provisional.	0
NZ_CP030771.1\|WP_138957760.1\|669360_670209_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	2.09867e-20
NZ_CP030771.1\|WP_138957770.1\|682486_683329_-\|DUF1206-domain-containing-protein	gnl\|CDD\|377695	pfam06724, DUF1206, Domain of Unknown Function (DUF1206). This region consists of two a pair of transmembrane helices and occurs three times in each of the family member proteins.	7.08505e-12
NZ_CP030771.1\|WP_138957771.1\|683693_684431_+\|trypsin-like-serine-protease	gnl\|CDD\|214473	smart00020, Tryp_SPc, Trypsin-like serine protease. Many of these are synthesised as inactive precursor zymogens that are cleaved during limited proteolysis to generate their active forms. A few, however, are active as single chain molecules, and others are inactive due to substitutions of the catalytic triad residues.	5.84287e-29
NZ_CP030771.1\|WP_138957757.1\|665672_666275_-\|carbonic-anhydrase	gnl\|CDD\|238449	cd00884, beta_CA_cladeB, 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.	2.08989e-67
NZ_CP030771.1\|WP_138957764.1\|675085_675967_+\|universal-stress-protein	gnl\|CDD\|238182	cd00293, USP_Like, Usp: Universal stress protein family. The universal stress protein Usp is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. Usp enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae Usp reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, athough Usp lacks ATP-binding activity.	6.2601e-17
NZ_CP030771.1\|WP_138957768.1\|680517_681834_-\|cytochrome-P450	gnl\|CDD\|365848	pfam00067, p450, Cytochrome P450. Cytochrome P450s are haem-thiolate proteins involved in the oxidative degradation of various compounds. They are particularly well known for their role in the degradation of environmental toxins and mutagens. They can be divided into 4 classes, according to the method by which electrons from NAD(P)H are delivered to the catalytic site. Sequence conservation is relatively low within the family - there are only 3 absolutely conserved residues - but their general topography and structural fold are highly conserved. The conserved core is composed of a coil termed the 'meander', a four-helix bundle, helices J and K, and two sets of beta-sheets. These constitute the haem-binding loop (with an absolutely conserved cysteine that serves as the 5th ligand for the haem iron), the proton-transfer groove and the absolutely conserved EXXR motif in helix K. While prokaryotic P450s are soluble proteins, most eukaryotic P450s are associated with microsomal membranes. their general enzymatic function is to catalyze regiospecific and stereospecific oxidation of non-activated hydrocarbons at physiological temperatures.	1.20195e-73

>NZ_CP030771.1|WP_138965954.1|672353_673028_+|FCD-domain-containing-protein
MEPPALRRGEWERPAASRAEVAARRIAAMVADAEPGERLGTKEELRATCGVSVGTFNETLRLLQSRGLVTVRPGPGGGLFAAEQSAMRRLGNSVLALDAKEPDGTRADEARRIRDALVPLLVEDALWHGSPADVAALRQELTELAEAARQADPVAFADVDHRLRTRLAAVSPNSLLRSLYATLLPVAEPDAVEHLQERYEHHAALVDALEARDRDRALDLARSG
>NZ_CP030771.1|WP_138957762.1|671686_672169_-|flavin-reductase
MTEQDFRDLMAGVCAPVTVVTAAEGGAPHGSTVSAFASLSLRPPMVSVALDHGSGLLARILTTGRFGVNVLGAEQEELALRFAGRSAGRFDRIRWEYDHGLPRLPDAPGWLVCELTSAVEGGDHRLLLGTVVHARTATAAPPLVYGHRTFGTHSAFTPVA
>NZ_CP030771.1|WP_138957761.1|670448_671645_-|acyl-CoA-dehydrogenase-family-protein
MTTTGTAASTDAEFVSRATALQPLLREHAPRIDADRKLTDEVIDALADAGLFKLTVPRRFGGHEADMRTLVDVSAELAEADGSTSWVVAVVNTCNWLAAALFPLQAQEEVFGADPDARVTGVFSPTATSRKVEGGWRTTGRWYYNSGAWHSSWAVLGIPLTDEAGEVVDQAMALVPRTDLEMQDVWHVAGMRGTGSNCLMAEDVFVPEHRVVSVPRALAGEVPATHGETGLFRSPLSPLLALGLAGPQVGLGRAALKLVSEKAASKPISYTYYESQVDSVGVQLQIAEAAMKIDTAQLHVHRAAADIDGAAARGGELDVLTRARVRADSGHAIKNVLESINTLLDVHGGGAFADSNPLQRIWRDASTAGRHAVSTPAVGMEIYGKLLLGVEERITPFV
>NZ_CP030771.1|WP_138957760.1|669360_670209_-|methyltransferase-domain-containing-protein
MSADWQWDDTLFSGTAAYYGRGRLPYAPGLADALTGALDLDGRGRLLDVGCGPGTVALRLADAFAEVVGLDPDAGMIAEARREAAGQGVAEKASWVRARAEELPAGLGTFTVVTFAQSFHWMDRDLVARTVRGMLRPGGALVHLSDLKAEDRSVAGLPHPPVPYAAMDELVRRYLGPVRRAGRGVLPQGTPGGEAAVFARAGFSGPERLVVPGGQALERTADDVVAGVFSMSFSAPHLFGPRRGDFASDLRALLRKAAPAGRFAERQPSTEIFLWRTAPTGR
>NZ_CP030771.1|WP_171075619.1|668867_669020_-|hypothetical-protein
MEKLIAKMAKDDVWNQWTALNSPKASGKEGCISADKSGCISVSAKSGCIS
>NZ_CP030771.1|WP_138957759.1|667509_668757_-|hypothetical-protein
MNGQPSADVIAQIQDIPIYRPYVERGHFPILEKPEIARGFPDNWMTPTLAGALAAGEAEFVLSTGTNHARMQIIRPPYFLLNSYYRLWSEHPDIADTWHEGCRRVSLTTVLATEHVARVNARKRGGPRAEPDPLPDLDQRRLDERTFYVNLRRDPALWDRADVERMIEEIRTAQTAHPRGRYHLDCSGPHLAHLVRKAVDWGLWASFPRPASIVHAYEYAPLNVRRYLHHHFACPVVDLFGSTELGYLFYSDRTGRYRPYLDRMSVELIPVEPGSRIHSLIVTSVRNPHMPLVRYRSGDCVRTADGSPDPDRITRFCGREKELLKTPHGPVAQGDLDDVVAGASPRVFVHQLDARDPSRALLRYTTFDGAPLAPVEADALRQGVAALTGRNSDLRHQEHIPIGGSGKYAWLAKDT
>NZ_CP030771.1|WP_138965939.1|666905_667415_-|hypothetical-protein
MTPADLASLLGDALYAEVVAHFAATADAPREYVERQVTECLRYLYLVSRHPDRLSGLFLPVEQEIDEIWHYLILQTREYRDLCERRLPGGFFIEHRSIAYEDYQREPGREQAIEEALRWIPLYAREFGPFDEGALPHWTIVRFLHEQLGMELSEISELTPTEPQGTGGS
>NZ_CP030771.1|WP_138957758.1|666343_666811_-|hypothetical-protein
MKHLSTDRPDDRACPTRTRRRIRPGPAARARHWAVTTVIVLLSLLCGGAAPAVAGAAPDATAPSRLAAPQPPPATMDTRERTLRDSEVPHPPPHVVRGRAHTTPAHARAATPQARPDAADPAARTARNPTGPRPGAPVPARPGAQLLVLHCVSRS
>NZ_CP030771.1|WP_138957757.1|665672_666275_-|carbonic-anhydrase
METFITHARGMTARIAERREEQETFGRLAAGQSPLALFITCSDSRVVPSLITGARPGDLFELRTAGNAVPPYEAGRPASSEGATIEYAMRVLRVADIVVCGHSHCGAVGAKARGEDLAELPAVRDWLDRQLSSELPADDGPAVAAAVQRHVREQLVRLRAYPCVSERLESGDVRLHGWYYEVHTGLVAAHHAETDLFLPL
>NZ_CP030771.1|WP_138957756.1|664046_665627_-|SulP-family-inorganic-anion-transporter
MKRPSVRDFATLRADFTASIVVFLVAVPLCVGVAVASGVPAELGLVTGIVGGLLTGLLPGSSLQVSGPAAGLTVLVYEAVQEYGIAALGALVLIAGLLQLAMGALRLGRWFRAISVAVVQGMLAGIGLVLIAGQLYALVDAEAPASGLDKLAELPRLAADTAGSGDALAAFAVGTGTIAVLVLWPRWRRAARVLPAPLAGVALATLAVFALDLSVAKVEVQGLVDAVQPPGGDAFSALVEGGALAGALGTILAFTLIASAESLFSAAAVDRMHNGPRTDYDKELMAQGAGNAVCGALGALPMTAVIVRSAANVQAGARTKASRVLHGVWLLAFAAAFPAALGVIPVATLAGVLIHAGWKLIPVKAFGPLWREHRGEALVLAVTALAIVATNMFEGVLIGLALAIVKTAWDTSHVHLEVEGLEGTGTIRVRVVGNATFLRLPKILDQLEALPGDRRTELDLSGLRHLDHACSTALTIWAERHGTVTASGGDTPPAGSAKDRQEDDDCEEHREHKEHQDHKEAAGARR
>NZ_CP030771.1|WP_138965956.1|674049_674868_+|carboxypeptidase-regulatory-like-domain-containing-protein
MARLAATAALALATLALGVPSAQAADADRAPRRAPDDAFVVTLSSDVSRTDFTHRKVKLSGTVTRADGTPVAGAPVKLHKTVLYNTWNPWGDPIDPIERETLPLGTLHTDAEGKFTVSGVPADRWLDRDSIHLFPRHEVEFQASYDPGDPSDGHFYFAETTVGVRSVDSSLTYKVNKKKVRAGDTLVVTGKVTWPAGHGPVAGTRVLLRTYYESSYDAKTTTDARGNFTVRAKIRGYDRDFVIFSTPKDYYITGASESLPVTNVTPRPRPAA
>NZ_CP030771.1|WP_138957764.1|675085_675967_+|universal-stress-protein
MTRAIAVGVDGSAESLAAADWAAVEAALRGAPLRIVHAWLPQSTDVTLARNGDEQVAAADAFVREAVARVSGRHPDLTIASEVVQATPVDTLLKEAERSEMLVLGSRGHGALVGFLLGSYGQQVIADAPGPVVSVRAGTGTDASARADAAGDVVVGQHGEPEDSEAVLRFAFEAAAARGAAVRAVRAWTLPPLYSYNTGVLQVADEAGGLEPLEQQALTRALAPWRERFPDVPVVEHVEIGSAGQVLLAATPDASLLVVGRKTRRSPIGTRIGSVAHAALHHAGCPVAVIPPA
>NZ_CP030771.1|WP_138957765.1|675980_677633_-|alpha/beta-fold-hydrolase
MKSPKPTLRVRVLAPSLAAVLAALPLAGCSTEGGHGSEGERADAATRPELQRFYGQRLKWRDCGDVECARLTVPRDYAHPGDGKTFVLPVARAATADEGRRIGTLVYNPGGPGESGVADLKEGGAESFGAEARARFDIVSFDPRGVAGSRPALDCPEDEEDTAEDDGAGAQPPVPRTAAARAQALADARAEATACRRGSRGLLQHVGTRDVARDLDVLRAALGERKLTYVGWSYGTHLGSRYAEQFPRRVRAMVLDGAVDPSLGWAQRALSEGTGFRRAVDDYATRCADVVGTGCPGASPKEIRRLIHGLYARAEHDPLPVEGEEEGLGATEVVDAVSMAMYTPEEQWKPLSAALRAAARGDGTKLAELSEAEMDEEAETDEEADGSGAPEPAPRSRSAGTAVDDSDGPGDASLDNSDAAILAVSCADTAYPRTAEPYWDALDRAEKKAGLYGVSSVLSVLACKDLPTGTPKPRRVAAEGVAPVLVVGTTGDPATPYEEAESLAEQFPGGMLLTYEAPGHTAYGRGDACVTKRVDGYLVGLRAVPDGTTC
>NZ_CP030771.1|WP_138957766.1|677759_678185_-|alpha/beta-fold-hydrolase
MHGGLVDSRFYEPNLGPLAGHFHVYTPERRGHGHIPDVPGPITYELMADDTIPFLEAVVGEPADLVGHSDGAFVAMLVAMRHVVEMYEALPRAELAVVPGTSHFLTQEKPALVNALVLDFLGKEPVRTVAAIRRAQEPQAG
>NZ_CP030771.1|WP_138957767.1|678204_680400_-|glycoside-hydrolase
MRSPSRVLPALALALGLAAGTTSPSGASDAAPRHPTATASTARSPVAYENVLDLEGVPKAASPGEFNPVNVFADRGAWHAYALPEADDPTTYGGFTGPLYIAQEYPWWLSRSFSRLRLKEAERTLDLAGGGAPRFTSLPGLLRQGYRLDGLDLTLELRFATDRTALVRARVHNSGRTTRTLAADWSGGLLRPEKGPQRDAPALTATARGVAVDFARVREKWDYLTDGTERFQITHREPVRTTLDHDTYRTELAAPLRLAPGAARTLDWAESYTFTAPEQAREGAAVRRALSRPAAVAAAGDARWRRYVAAVTDSVPAARRRLAVKALQTLATNWRSAAGRIRHDAISPSLSYKWFAGGIWAWDTWKQAVGTARFDPRLAESQLRAMFDHQIRPGSASRPQDAGMIPDAVFYNDPSDGGGNWNERNSKPPLAAWAVREVYERGGDRGFLREMYPKLAAYQAWWYRNRDHDGDGLAEYGATVDPANDSAEERRLAAAWESGMDNAPRFDAALGTSVVANQNASGRVTGYSLTQESVDLNAYLAADQTHLAAIAREVGDKAGERHWRARARATHQAVRERMYDPTSGWFYDTDLADGSRLTGRGRGIEGAIPLWTGTATPAQAAAVRDKLTDPGEFATPVPFPTVARSSPYFAPQRYWRGPVWLDQAYFAEAGLRRYGHTAEARALTDRLLTHATGLTGRGPVMENYDPLTGAPLNSPNFSWSAAALLPMLSGR
>NZ_CP030771.1|WP_138957768.1|680517_681834_-|cytochrome-P450
MEIPGPEARPDGGVGAVTAAGGLHTYQLRLHAAYGPVVRFQLPGAEDAVSVADPVLLEATAHIDKRPERLFEFLAPLCEADNLQVLAADQHTPWRRLLLSVFAGRPSHERHFARFTALATDLADRWAARAGGEPVELQKDLTALTLRMICAYSLGGDTEDPEKVTEAFETVLTEYLGRLYQAPVPGTQDERARRAEAALAYLRATVDQVIAAHHRSGGRADRSDLIGALVEAGQSPARIRDTVMVTLLAAHHTTGVAVSWTLHLLGRHPEVAARVTEEVDRVLGDRSAPTYADLRRLTYLDMTLKEAMRLYPPGPYGARETTEPLTLGEYEIPAGTTIFYPFWAVHLNPDHWPEPERFLPERFTPEETAKRPRFAYIPFGLGPRGCEGAALATVEAQLVLAVLLKRLTFRPVPGHQVTPIERFVLWAADGIPMRVGVR
>NZ_CP030771.1|WP_138957769.1|681975_682383_+|DUF3224-domain-containing-protein
MRASGTFKVADFTPVAAPSPGIETAVPVAVATMAKQYEGEVVGHSTTLFTAAADQSTGTGTYVAMESFEGALHTRSGTFNFAHSGTTVDSRKQGEFFVIVPGSGTGDLAGITGTGGIAVDEDGTHRLWFDFDLGQ
>NZ_CP030771.1|WP_138957770.1|682486_683329_-|DUF1206-domain-containing-protein
MGFDGVVRNGTGRARRLARGRVVEVAARAGFVARGAIYVLVGVVALRIALSDDDGKQADRGGALTELAQKPFGEALLWLLGLGLVGMALWRLSEALFGQAGPEGRKPGKRLLSAARFVFYGVVSYLVLAYVTGDKGSGSGSSDRQADDFTATVLDWRGGQWIVGAAGLGVVAAGLWMIGRAVLRKYRRRLRMGEMSAPVRRGVDVLGVVGGCGRGCAFAAAGVFLVVAAVRHEPGEAKGMDDTLRSFSHTAGGPWLLVALAVALMAFGVFSWASARWRKV
>NZ_CP030771.1|WP_138957771.1|683693_684431_+|trypsin-like-serine-protease
MRISRLLPAVAAVALTVLGLAPTAAAQASAAERAPAAPSTTAAQPIIGGGYASNAPWAARLFSNGRQTCTATIIAPTWILTAKHCVSGGGLSFRIGSLDQTTGGTQANGVSVTSNPSADLSLVKLDRSVAGTYSPLGQPGSVTVGQSVQVYGWGATSQCGQEINCQSRLLKVANVTVTGGCRDAYQGQAICARRGNGITAGGDSGGPMMANGLQVGVASTSDRQTTTAYTNVTAYRSWIQSVAGV
>NZ_CP030771.1|WP_138957772.1|684482_685439_-|MEDS-domain-containing-protein
MTRTGFVHQALCYGADEEFLEGTLGYVREGLEAGDALLAVVAGGNIDLLRDALGGAAREVEFIDCLDWYHYPSRTLGQYHAYCTAREQGGARRVRVIGEPVWTGRTTLEVQEWMRYESLLNVAFAESGHWILCPYDTRALPEAVITTARRTHPELAVGDDALLRNDRYAAPADFYAECDEAERESAAPAFRAAAEIPFERGRTTVARAAAAEFARGRALAEGRVQDLVVAVHETVVNAIRFGGGHGVLRLWSEPEYLVCEIADGGRGHLPSVPAFPGHLPPAPRAASGHGLWVVRQLSDLMTERLGPDGSLVRLYFRR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_3

1206618-1206733

Orphan

Consensus_repeat	Method
GGCTGACGCGGGCGGCGCGGGCGGCG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP030771_3

>merge|NZ_CP030771|3|1206618-1206733|CRISPRCasFinder
GGCCGACGGGGCCTGCGGGGGCGGCATGGCTGACGCGGGCGGCGCGGGCGGCGCGGCTGACACGGGCGGCGCGGGCAGCGCGGCTGACACGGGCGGCGCGGGCGGCGTGGCTGGCG

>NZ_CP030771|3|2|1206618-1206733|CRISPRCasFinder
GGCCGACGGGGCCTGCGGGGGCGGCA	TGGCTGACGCGGGCGGCGC
GGGCGGCGCGGCTGACACGGGCGGCG	CGGGCAGCGCGGCTGACAC
GGGCGGCGCGGGCGGCGTGGCTGGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138958033.1\|1215216_1215501_+\|acyl-carrier-protein	unknown	unknown	gnl\|CDD\|376348
NZ_CP030771.1\|WP_138958032.1\|1214204_1215200_+\|3-oxoacyl-ACP-synthase	unknown	unknown	gnl\|CDD\|238423
NZ_CP030771.1\|WP_138958027.1\|1189282_1189711_-\|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl\|CDD\|274679
NZ_CP030771.1\|WP_138958028.1\|1189863_1190373_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380345
NZ_CP030771.1\|WP_138958023.1\|1178168_1178729_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379112
NZ_CP030771.1\|WP_171075632.1\|1217802_1218687_+\|3-hydroxyacyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|224170
NZ_CP030771.1\|WP_138958029.1\|1190606_1191245_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP030771.1\|WP_138958034.1\|1216663_1217761_+\|HAD-IIIC-family-phosphatase	unknown	unknown	gnl\|CDD\|273757
NZ_CP030771.1\|WP_138958031.1\|1207160_1214195_+\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|237108
NZ_CP030771.1\|WP_138958024.1\|1180386_1181718_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370517
NZ_CP030771.1\|WP_138958038.1\|1223117_1223633_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380345
NZ_CP030771.1\|WP_171075631.1\|1178760_1180152_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP030771.1\|WP_138966055.1\|1215530_1216667_+\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|173847
NZ_CP030771.1\|WP_138958026.1\|1185490_1185892_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138958022.1\|1177621_1178068_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380387
NZ_CP030771.1\|WP_138966053.1\|1187104_1189021_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|367320
NZ_CP030771.1\|WP_138958037.1\|1222185_1223037_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|182183
NZ_CP030771.1\|WP_138958036.1\|1218727_1222030_-\|S8-family-serine-peptidase	unknown	unknown	gnl\|CDD\|173812
NZ_CP030771.1\|WP_138958039.1\|1223629_1223992_+\|DoxX-family-protein	unknown	unknown	gnl\|CDD\|379266
NZ_CP030771.1\|WP_138958025.1\|1183056_1185417_-\|protein-translocase-subunit-SecD	unknown	unknown	gnl\|CDD\|237276

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138958032.1\|1214204_1215200_+\|3-oxoacyl-ACP-synthase	gnl\|CDD\|238423	cd00827, init_cond_enzymes, "initiating" condensing enzymes are a subclass of decarboxylating condensing enzymes, including beta-ketoacyl [ACP] synthase, type III and polyketide synthases, type III, which include chalcone synthase and related enzymes. They are characterized by the utlization of CoA substrate primers, as well as the nature of their active site residues.	1.90903e-28
NZ_CP030771.1\|WP_138958033.1\|1215216_1215501_+\|acyl-carrier-protein	gnl\|CDD\|376348	pfam00550, PP-binding, Phosphopantetheine attachment site. A 4'-phosphopantetheine prosthetic group is attached through a serine. This prosthetic group acts as a a 'swinging arm' for the attachment of activated fatty acid and amino-acid groups. This domain forms a four helix bundle. This family includes members not included in Prosite. The inclusion of these members is supported by sequence analysis and functional evidence. The related domain of the anguibactin system regulator AngR has the attachment serine replaced by an alanine.	1.77114e-06
NZ_CP030771.1\|WP_138958028.1\|1189863_1190373_-\|cupin-domain-containing-protein	gnl\|CDD\|380345	cd02215, cupin_QDO_N_C, quercetinase, N- and C-terminal cupin domains. This family contains quercetinase (also known as quercetin 2,3-dioxygenase, 2,3QD, QDO and YxaG; EC 1.13.11.24), a mononuclear copper-dependent dioxygenase that catalyzes the cleavage of the flavonol quercetin (5,7,3',4'-tetrahydroxyflavonol) heterocyclic ring to produce 2-protocatechuoyl-phloroglucinol carboxylic acid and carbon monoxide. Bacillus subtilis quercetin 2,3-dioxygenase (QDO) is a homodimer that shows oxygenase activity with several divalent metals such as Mn2+, Co2+, Fe2+, and Cu2+, although the preferred one appears to be Mn2+. The dioxygen binds to the metal ion of the Cu-QDO-quercetin complex, yielding a Cu2+-superoxo quercetin radical intermediate, which then forms a Cu2+-alkylperoxo complex which then evolves into endoperoxide intermediate that decomposes to the product. Quercetinase is a bicupin with two tandem cupin beta-barrel domains, both of which are included in this alignment model. The pirins, which also belong to the cupin domain family, have been shown to catalyze a reaction involving quercetin and may have a function similar to that of quercetinase.	1.34621e-15
NZ_CP030771.1\|WP_138958023.1\|1178168_1178729_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.70723e-21
NZ_CP030771.1\|WP_171075632.1\|1217802_1218687_+\|3-hydroxyacyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|224170	COG1250, FadB, 3-hydroxyacyl-CoA dehydrogenase [Lipid metabolism].	4.73494e-92
NZ_CP030771.1\|WP_138958029.1\|1190606_1191245_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	6.40319e-09
NZ_CP030771.1\|WP_138958034.1\|1216663_1217761_+\|HAD-IIIC-family-phosphatase	gnl\|CDD\|273757	TIGR01686, modular_polyketide_synthase, FkbH-like domain. This model describes a domain of a family of proteins of unknown overall function. One of these, however, is a modular polyketide synthase 4800 amino acids in length from Streptomyces avermilitis in which this domain is the C-terminal segment. By contrast, the FkbH protein from Streptomyces hygroscopicus aparently contains only this domain. The remaining members of the family all contain an additional N-terminal domain of between 200 and 275 amino acids which show less than 20% identity to one another. It seems likely then that these proteins are involved in disparate functions, probably the biosynthesis of different natural products. For instance, the FkbH gene is found in a gene cluster believed to be responsible for the biosynthesis of unususal "PKS extender units" in the ascomycin pathway. This domain is composed of two parts, the first of which is a member of subfamily IIIC (TIGR01681) of the haloacid dehalogenase (HAD) superfamily of aspartate-nucleophile hydrolases. All of the characterized enzymes within subfamily III are phosphatases, and all of the active site residues characteristic of HAD-superfamily phosphatases are present in this domain. The C-terminal portion of this domain is unique to this family (by BLAST).	8.26378e-66
NZ_CP030771.1\|WP_138958031.1\|1207160_1214195_+\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|237108	PRK12467, PRK12467, peptide synthase; Provisional.	0
NZ_CP030771.1\|WP_138958024.1\|1180386_1181718_+\|hypothetical-protein	gnl\|CDD\|370517	pfam09471, Peptidase_M64, IgA Peptidase M64. This is a family of highly selective metallo-endopeptidases. The primary structure of the Clostridium ramosum IgA proteinase shows no significant overall similarity to any other known metallo-endopeptidase.	6.15036e-71
NZ_CP030771.1\|WP_138958038.1\|1223117_1223633_+\|cupin-domain-containing-protein	gnl\|CDD\|380345	cd02215, cupin_QDO_N_C, quercetinase, N- and C-terminal cupin domains. This family contains quercetinase (also known as quercetin 2,3-dioxygenase, 2,3QD, QDO and YxaG; EC 1.13.11.24), a mononuclear copper-dependent dioxygenase that catalyzes the cleavage of the flavonol quercetin (5,7,3',4'-tetrahydroxyflavonol) heterocyclic ring to produce 2-protocatechuoyl-phloroglucinol carboxylic acid and carbon monoxide. Bacillus subtilis quercetin 2,3-dioxygenase (QDO) is a homodimer that shows oxygenase activity with several divalent metals such as Mn2+, Co2+, Fe2+, and Cu2+, although the preferred one appears to be Mn2+. The dioxygen binds to the metal ion of the Cu-QDO-quercetin complex, yielding a Cu2+-superoxo quercetin radical intermediate, which then forms a Cu2+-alkylperoxo complex which then evolves into endoperoxide intermediate that decomposes to the product. Quercetinase is a bicupin with two tandem cupin beta-barrel domains, both of which are included in this alignment model. The pirins, which also belong to the cupin domain family, have been shown to catalyze a reaction involving quercetin and may have a function similar to that of quercetinase.	1.90241e-25
NZ_CP030771.1\|WP_171075631.1\|1178760_1180152_-\|tetratricopeptide-repeat-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.	4.27534e-08
NZ_CP030771.1\|WP_138966055.1\|1215530_1216667_+\|acyl-CoA-dehydrogenase-family-protein	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.	4.76412e-73
NZ_CP030771.1\|WP_138958027.1\|1189282_1189711_-\|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl\|CDD\|274679	TIGR03618, Rv1155_F420, PPOX class probable F420-dependent enzyme. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomyces, make F420. The Partial Phylogenetic Profiling algorithm identifies this members of this protein family as high-scoring proteins to the F420 biosynthesis profile. A member of this family, Rv1155, was crytallized after expression in Escherichia coli, which does not synthesize F420; the crystal structure shown to resemble FMN-binding proteins, but with a recognizable empty cleft corresponding to, yet differing profounding from, the FMN site of pyridoxine 5'-phosphate oxidase. We propose that this protein family consists of F420-binding enzymes. [Unknown function, Enzymes of unknown specificity].	1.33179e-09
NZ_CP030771.1\|WP_138958022.1\|1177621_1178068_-\|hypothetical-protein	gnl\|CDD\|380387	cd06982, cupin_BauB-like, Pseudomonas aeruginosa BauB and related proteins, cupin domain. This family includes bacterial proteins homologous to beta-alanine degradation protein BauB from Pseudomonas aeruginosa, which is involved in the degradation of beta-alanine. Also included are Rhodopseudomonas palustris Rpa4178 and Bordetella pertussis Bp2299, which are both proteins with unknown function. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	1.95372e-07
NZ_CP030771.1\|WP_138966053.1\|1187104_1189021_-\|hypothetical-protein	gnl\|CDD\|367320	pfam03068, PAD, Protein-arginine deiminase (PAD). Members of this family are found in mammals. In the presence of calcium ions, PAD enzymes EC:3.5.3.15 catalyze the post-translational modification reaction responsible for the formation of citrulline residues: Protein L-arginine + H2O <=> Protein L-citrulline + NH3. Several types are recognized (and included in the family) on the basis of molecular mass, substrate specificity, and tissue localization. The expression of type I PAD is known to be under the control of oestrogen.	5.34156e-143
NZ_CP030771.1\|WP_138958037.1\|1222185_1223037_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|182183	PRK09986, PRK09986, LysR family transcriptional regulator.	1.91392e-37
NZ_CP030771.1\|WP_138958036.1\|1218727_1222030_-\|S8-family-serine-peptidase	gnl\|CDD\|173812	cd07487, Peptidases_S8_1, Peptidase S8 family domain, uncharacterized subfamily 1. This family is a member of the Peptidases S8 or Subtilases serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	8.18716e-82
NZ_CP030771.1\|WP_138958039.1\|1223629_1223992_+\|DoxX-family-protein	gnl\|CDD\|379266	pfam13564, DoxX_2, DoxX-like family. This family of uncharacterized proteins are related to DoxX pfam07681.	2.77093e-09
NZ_CP030771.1\|WP_138958025.1\|1183056_1185417_-\|protein-translocase-subunit-SecD	gnl\|CDD\|237276	PRK13024, PRK13024, bifunctional preprotein translocase subunit SecD/SecF; Reviewed.	0

>NZ_CP030771.1|WP_138958029.1|1190606_1191245_+|TetR-family-transcriptional-regulator
MSSKDAGAPAPRPGGRPRDPAIEEAILKATRARLATDGYARLTIGDVVADAGVTRPTLYRRWANKRELVVDALDYGLRKQREAYPPMDLERMTPLEAFTEAVRRLDPRYHNERAMALHGNFMGEAEREPELFTQLREHGNEPRCAELTRTLRHLQDVGAVRADADLDAVVTLCFGSYFGDYLRAGRSTPADLADRVVAVLWPTLRAHERPEA
>NZ_CP030771.1|WP_138958028.1|1189863_1190373_-|cupin-domain-containing-protein
MSTSVPRLTVVQPGEGHHAPIPGFGADFKLSSAASGGPLSIVEHPFGVGVITPPHLHTREDEYSIVLEGEIGFRSDDAETVIGPGGYIIKPRGQMHAMWNAGDTPGRIIEIITPGGFERYFQEIADLVAASTSDRGAFDELAEKYGLTYGHPDWFDDVVRRYGLTPPKR
>NZ_CP030771.1|WP_138958027.1|1189282_1189711_-|pyridoxamine-5'-phosphate-oxidase-family-protein
MALTPEEREEFLAQAHIAALSVDAGEEGRAPVTVPIWYQYEPGGEIWIMTGKESRKAQLIAAAGRFTLMVERVEPSVRYVSVEGPVVATEPATREQLHEISARYLPADKVDGYVEEAWKGHGEQIVVRLRPQRWISSDLGSI
>NZ_CP030771.1|WP_138966053.1|1187104_1189021_-|hypothetical-protein
MALAAGAAGVLVATGATAMADAATPAPANKPDLRADVNRDGRVDVEGDSDSRGENTWTRERGAIVLPNIDDDAKRCPVKDSNGRPLSSAKLARCNDASDTKVNGAKDALDLARLRTVPLPDAAAGSHGTVKVVGAGAKKARLFVHRDGRWSLLKPTDKLTVKELRSGVELGIEATDVVRDAAQWNGDITVRFTVGGGDGPARSDDVVLRTAPVLTQHHLQKAQEVLVTKVPGRDAYSKAQQKFVKDLAKQVKDAGISKPLTTFTKYGDIWAQDFVEPGYASMPGPDGKPRTMRVLIRSAQLDRPAGRELFEKLRGPDVGVVQVAKAGANEEWTLNSMGNLETIPPYKLGNKDYPAGRIIQGYRKDNGSKPAKSMRTFLKSQGAQDPLLLDTSWLSVGHVDEFVQFLPADTERGWRIGVADPKAGVELLRKAQREGHGAKKMFSVPRGSDVPAPKETIDKVLGSAKFKADNKLAAERIEANLATLKRETGVTDAEIVRVPGLYVRDGQGGSGLSNSRKLRRLGPDSLRKFNQLRGDDNRADAGGKGRTRAAAAWQNSAYIPGAVNGVLLSPTRYLAPQQWGPVIGGKDIFTEAVNSVYAKAGFTTTYIDDWYTYHIGMGEVHCGTNTLRDTTAPWWPKA
>NZ_CP030771.1|WP_138958026.1|1185490_1185892_-|hypothetical-protein
MQYRARSARLAASVLSVVVAVLAFAVPSRAPGAVPAVPTALAAPDRSHSDSVGPHAPDLPRVVHATVAHPHHAHLPHPPYPATTAADRAPHRPVGGPAAPARGTAPARQHPDAGPRPRGPPPPMSNDTVQDAA
>NZ_CP030771.1|WP_138958025.1|1183056_1185417_-|protein-translocase-subunit-SecD
MPRAPLWRAIVALVAVAASLFLALTQSPRLGLDLRGGTQIVLETKDSPTVKADEAATRRAVEVLRQRVDALGVSEPSLAQAGAKRIVVELPGVRDPREAAEVIGRTAQLTVHPVTGATDRPGKAAPAADGSRTLPDPDRPGGHLRLGPTALTGDGVKDADAVLDQQALNGWYVTLDFRKKAADDWARVTGEAACAPRDAPQRRVAIVLDGKVISAPGVNADVRCGTGITGGSTQITGGFDEGEARDLAALVKGGALPVPVDVVEQRTVGPTLGAAAIDASTQAALIGLVLTGLFIIVVYRLLGALATLALALYGLMSYAALLAVGATLTLPGLAGFVLAIGMAVDANVLVFERAREEYLGPRALRPDGESRTAGAPRSMAKALHTGFTKAWSAVVDSNVTTLLAAGLLFFFATGPVKGFGVTLSIGVLVSMVASFVVTRALADAAVRRRFVRARPRLTGLATTGRVRTLLARRNPRPVRHGGRWLGAGALLVAVAVAGIVVRGLDLGVEFTGGRLVEYSTSQRLDADTAREAVADAGFPRAVVQESGEDDITVRTGELSDGEQERIKKALAGPGGEVTVERDERIGPSLGAELRQKALVALGIAVAAQLVYLSVRFRWTFATAAVTAMVHDVLLVVGLFAWLGKTVDSVFLAAVLTVIGYSVNDTVVVFDRVREARRRDPRAELADLANKAVVRTLPRTVNTGMGALFVLAALAVLGGDSLADFSLALIAGVVLGMASTVSVAVPAAVLLERRSPAPRRPARPSEGPRPRSPLEAGRRRSGDGAVV
>NZ_CP030771.1|WP_138958024.1|1180386_1181718_+|hypothetical-protein
MASDTSGIPTRTRRKRLRVALAAGVTLAATLSATGGAVAHPEPSAAEPSRSVEYFGKDGHPRHTEVPAPAPLTREERSEIAGGADGDVVPIVQNGPVGTKADVVFIGDGYTAAQQEDFHADVRTKWAEVSKVEPYASYKNLFNVWAVDAHSRQSGVSGDPTSNVRKDTALGSSFYCDNIERLLCVDTNKVEAYARKAADPDVVIVLANSTKYGGAGYNDITSPSGYDGIATGSSDNAQSSQVVVHELGHSLGKLADEYWYDEYGTYTGAEPSWLNSSKLTAAQLTAQKKKWYRWIGQASPDGGTVGAYEGGNYYPRGLYRPTDNSIMRTLGRQFNLPGREAMIAGFHRHASVATSATPTGSEVRRKQRVAVETGAGVRLRWYVDGRPAKKGDDARAVTPRSLGVPADGRAHTISVRAKDTTKAVRDPALRKLLTSELTWHVTR
>NZ_CP030771.1|WP_171075631.1|1178760_1180152_-|tetratricopeptide-repeat-protein
MAEISPEGARLDDPAEIGRRVLRLRTERGLTQRQLAEPAYTPAYVSTLESGKVRPSEAALRHLAGRLGVGYEELATGRPARLATDLRLRLTDARRALATGAPEDAAAVFRTLHEEAVAHALPSEQAAALQGLGDCLLESGELTDARDCFAAVERLLADEPLPRRVPAIRGRATAHLLTGELRYACYLLETTLDELNAAGLHDPDALLLLYTASIAPYMDMGAHARAAHAAELALALAPSVSDPALVAHMHRGVARTLIAEGRTAEADASLAKAQELYRQLHIRTELAHCHWMRGYVHAQDGDLDRAESELRTARDMLASKRAALFTEQVEVELADVLRRRGRADEAEALLRPLLVSGADGADTGPLGAERGAVHAGGAHRLLGLIAEERGDTESAEEHYCAALSLLERSSAAGDLADLCRLLGDLLRRTGRVEAALDAYRTGLGHRAAPGTTTLGPAPATPPL
>NZ_CP030771.1|WP_138958023.1|1178168_1178729_-|GNAT-family-N-acetyltransferase
MTSDGGTTAERPTAPDKAPERPVLDWPTTLATERLTLRPVAEPDVPHAVRLWTDPQVRRHLGGPVSADVVRAREQHCVGVPGAFAVERHDGAVLGLVVAEPDGHDGRTEVSYQLLPEHWGQGYAREAVHAVVGWARQAIRSAIPGVVAVTQRANTRSRHLLDSLGATPADHFVAWGEPQVLYVFPD
>NZ_CP030771.1|WP_138958022.1|1177621_1178068_-|hypothetical-protein
MGQGIPAVLPLVSTVVAEAFDRWSPPLHEDFEKNAHNGRVGSSLLAETASVRIWETRLGPGERIPVHRHVLDYVWIALTSGRARQHLGDGSSREIAYERGHTQRFRIAEGAFHLHDMRNIGEEVLSFLVIEEKAGPNEPLELTGAQRH
>NZ_CP030771.1|WP_138958031.1|1207160_1214195_+|amino-acid-adenylation-domain-containing-protein
MTHPSPPGPEAVAVIGVALALPDADGLDALHHNLVEGRVSVRAPGRDRVHYAGAAADDAYLPLAYLDRIDLFDHRFFDLSLREAELMDPHQRVTAQLAHQAIENACYAPRDLKGSRTAVVLSAPEPHYAGLYPDDDPQQLLGSHPSATAARISYLFDFAGPALVVDTACSSSLTALALAVDQLREGRADLAVAGGVSLYPVLIRERDYVPMLGIVSADGVCRPFDAAADGSTAGEGGGLVVLKRLSDALADGDHVHAVVRGVAVNQNGFRATSMSAPSARGQSDAIVEAWRQAGGAPPDYVECHGSGTRLGDVIEAEGLRQAFAEAGVDGDAGVGGGLGSGEPCGISSVKGNIGHINHAAGVAGLLKVLAGLRHGTRYPNPNFSTPNPLIDFSGPVRIDTGAKAWEPAPGSPRRAGVSSFGLTGTNVHAVVEEPPPVPEAPAAPEPGTELVTLSAKSPRALAVYARRVADFLDETGHRLPDIAHALNRGRDDHPYRWAGTARDRRELAAALRSVRHAEREPSPAAPLVLLFSGDAELGDATWAALGAAFPRLADTDAGADDGSPGARLFARQLAAHRLAGALGLTGARLVGSGVGNLAVRSVQSPATADEARRKATDTPITSQVDESGLRRAARGLVDEGAVVVELAADGTLARQLARVAPELPVVRLYADPTRDGVLAALGRLYALGADIDWNAYYAGARTRRIEAPTYPFDADAVSCWCLPPGGPPRDHAPAPAHAPAPARQTEPGDTEAALAALWTRVLKADGVGPDSNYFELGGTSIAGITVLRAAEERFGARLTFADLHRNPTLRALAARIDAVRAAGPERDDWTITPLPRPGRLPLSFNQEQLWYLDRLNPGSPLYNIPANTRYVGDFDLGAFRGALRDVVDRHEVLRTRLPDEDGTPYAVADVPEPQVEFVDLTALPVGERTEELARAITAEATAPFDLGRGPLLRTVVVKAAERDHVVLHTVHHIAFDGWAPAVFFRELSACYTARLAGRRADLPELPVQYADFAAWQRRWLDAARVERGLTYWRGQLRDLDSPELPLDRPRPPAQSYRGGSVKFTLDEELARRLRAFSAGESTTSFVTMLAVVDALLHVWAGRRDVVVGAATTGRFNPLTHDLIGYFNNLLPFRTKVDPGIGFRELVGRCAATATGVLDHEEIPFARIVADADHRDPSRHPVFTVCYTHQNTAAATLGLEGLRPEALRGDLAGVSGVAPGTSKFDLTFGLYDQDDSPMDGYLEYAVDLFDAATAHRLVGLFQGIAEAVVSDPDRPLADLSRLLDAPAGPDLTEPSLLVGERRTLPDVRLVSEVFQEHAARRPDEVAVIDAAGEHTFQEIDRRANRLARQLIAHGAGPESTVPVLAARGAGLVVGWLGVHKAGAAFASLDPAVPARRVRSVLAGVDAAAVVLGEGMTVPATDGVPLVRITDAAGDPAPDEDTAPPQRAGVRNLAYVVHTSGSTGLPQGCEVEHGGLLNALAWYADEARPRPGDRLAQLAATGFDLAVFEVMAALRHGTPLYFVTDPLQTPDKLLGELAEHGVTLACMPTPLAETVLAELPDAPDPALRLVLAGGDRLRVRPPRRAPFGLVNVYGPTECTVCVTASRVADAETAPDVVPDIGRPLPRVRVHVLDPRLKAVPRGGLGEVYAGGAHVGRGYHGRPGATAARFVADPYADEPGARMYRTGDLARVRADGTLEFHGRADDQLELRGHRVEPAEVERALLAHPRVREALVHAAQQPSGAPLLVAHVAGDDVPEEAELTRWAARALPEYMVPGRVLRHAALPRTGNGKLDRQTMRKRDMSDRDTTNELTAVVTAVTPGAVLDDAGRGAERVLATIWTELLGVARVAPDDNFFRIGGDSLLSVGIAARATRAGLPLTPHDVLSHPTLRDLAAVAAKGAGPGAAPRPAAAVPAPREPVPPAPLVQALLTAAPDGARDFITPVLLETAAGIGADAVRAAFDRLVEVQEPLRYRFLHNSLGWRIECAEHEGARIVDHRVLPPLDEEQLQAYLEADLDELLADVDPGRGPVLRARFYDRGADRPGVVVLAVHHFVFDSTSFVPLIEDLNAAFADNAPAAPRRAAWRAWTHLLRAMAASDEVAGELPYWKGVLSAGATARPVPEKGADGAPSGLLRRRVAPDRVAARLTESGPTGQSAALAAVATAWSRWRGEPDAFVSTVGMGSSPNALWNGDRSDAVGWFTHLFPAHLRVAAGARVADALPGVATALRSVPNDGIGYGVLRHLSPATPAVAGVRALPEPQVLVEHVANANDGLTKLGGPHVRPRPMTLVTVPHALLTQVPIVVETHVLAGALELGVIHRGSVAAADMEDFADHLVEAFAELAADEGR
>NZ_CP030771.1|WP_138958032.1|1214204_1215200_+|3-oxoacyl-ACP-synthase
MTAIKAAACYHPDRVLPVAELPGLAELGDGERETCARLGIDEVRADETLSAFDLAVRAARQTLSEARLDAAELGALVLIDARVPDTLMSSAATRLQALLGAERALTFSVGGLGCVSLTPALLTARGLLAADGDLDHVLVVHGSKPPTPLRYRHPVTVSGDGGAAAVISRRGPVRVLDVVQETNGAHWDLFRVDYRDRPTARWREECRDIPQYSFRLAVESRIRLRALHQRLLDRNNLVPGDISRYLSHNLSEGTFRFTEEALGIKISTACFDNLRHYGHLGPNDVLLNLRTELDRGGLAEGQRAVLLSASPVAAWSLLLVEIGDGATTHYL
>NZ_CP030771.1|WP_138958033.1|1215216_1215501_+|acyl-carrier-protein
MDTPNGTDAADAASVTEELRAYLSGALGREPGPDEDYFALGLVTSLFAIELVNFVEQRYGIEVTVDDLDLDHFRTLGRLREFVLAKAAGRGAAA
>NZ_CP030771.1|WP_138966055.1|1215530_1216667_+|acyl-CoA-dehydrogenase-family-protein
MGARFADAVRQDAAAWDARGELPAEVRRALARDGLLGADLPRRHGGLGATPAELGEVCARLGGVCGSLRGLVTVQGMVGAALLRWGTAGQRERWLPALARGELIAAFAATEAEAGSDLAAVATAVERHGEAYAVSGEKRWITFGEIADVYLVLGRTGGRPAAVLVEADRRGVRREPVRGQLGLRAAQLAHVTFDDVRVPPENLVAPPGFGLSHVAGTALDHGRFTVAWGCVGMAEACLGAAAEHAVRRAQGGVVLAEHQQVRALLGRAVVDGRAARELCLRAARLRAARAPEAVAETVAAKYAAARAATSVAGSAVQILGAAGCAPDSLVGRCYRDAKVMEIIEGSAQVSELTIADHLLRAHGHGRAGRRPEDEGEGR
>NZ_CP030771.1|WP_138958034.1|1216663_1217761_+|HAD-IIIC-family-phosphatase
MSTPPRGPHGTTAAGPGTDPARPPEPTVKCLVWDLDDTLWDGVVLEGDAPVPFAAAVRTVRALDRRGVLHAVASRGEHDVAAAHLAAHGLDTLFTVLEVGWGAKSRAVERIAAELNIGLDTVAFIDNDAVERAEVAAALPDVRCYPAHEAELLTSYPEFTPRFLTDESALRRDLYRTERRRKAAEAEHTGPPAGFLASLGLVLTVRRATGADLARAHELTVRTHQLNTTGRTFGPDELRGLCADPGHEVLVAGLTDRFGSYGTIGLAVTALRDGATVLELLLMSCRVMSRGVGAVLIDHIVATALAAGRRPVAEFVPTDVNRQMLVTLRFSGFAVVADAGDRLTLAIDPDDPPPARKHPVRVVTA
>NZ_CP030771.1|WP_171075632.1|1217802_1218687_+|3-hydroxyacyl-CoA-dehydrogenase-family-protein
MVQDGVGGGVVGVVGAGTMGVGIAQCLAEAGHRVVAVDPEEAALASAPARLRDGVRLARMVRGATAAVPPDQALAAVTWTARLEDLAEAWFVLDCAPERIPLKEKLFRDLDEVCPPGAVLATGTSAIPVERLAARTGRPDRVLGLHFMNPAPMKEAVEVVRGPRTSDETLDTALALLAGIGKKGIVVADGPGFVSNRVLMLTINEAATVVRQGTADPATVDRIFEECFGHTMGPLATGDLIGLDTIVDTLYVLLECTGDQRFQPCEGLEALVADGHLGRKSGRGFHRYPARAPR
>NZ_CP030771.1|WP_138958036.1|1218727_1222030_-|S8-family-serine-peptidase
MAAVLSGALLTGAAAADTGTPRDGAAAAAAKSGRGDRAGKTATVTLITGDRVVVARGGGEVVRLIRGKGREEVTISVRREAGHVFAVPQDAQELITAGRLDRRLFDVTQLVKDRYDDARSPSLPLIVGYRPGKANSFRAADTFKGRAHDRRELPTLGGEAFSTPKSDTADLWSALTRGTGGRANVRTTAVPAVAHVWLDAKVRPALDKSVPLIGAPTMWQAGYTGKGVKVAVLDTGVDQTHPDLKGVEVIEKNFTTAPDAKDRMGHGTHVASTVAGSGAKSGGKYKGVAPGVRILDGKVISEEVGGGYDSDIIAGMQWAVDNGAKIVNMSLGSLDTQGTDPMEEAVARLSGKALFVASAGNEGPGAGTLTTPGSAPAALTVGSVDKQGRIAEDSSHGPSADGVAKPDVSAPGVEITAAASTDGPAGTEGNGYVAMSGTSMAAPHVSGSAALLLQQHPTWTGPQLKAALTGSAKPNPKLNPYQQGAGRVDLTRAITASVVSQPGTLAFGTQAWPHTDDKPVAKTVTYRNYGTKPVTLKLSTTSVDPAGRPGPAALFTAADTELTVPAGGTAKTTVTVNTKLGTADGTYGGSLLAAGDGQSVRTGLVVEREVESYDVTFRHLDAGGESASTYVTTLTDPATQKKLQVPYRDGEATLRVPKGTYALESSVYDPSGRLTVFVQPKLTVGAKKSITLDARKAKPFAVTTPDRTARLAEAHISYEDQATGISGSWSLTDATAVRTAGLGPESPTFHAQYSGLWKVPGATKKVDYRLAFGRTGTWFTGLKHATTKAELAEMKIGAGSSAARRKGTLAALPIGTNGYGPNLLSPTKLNLPASGTSYVTTKGLRWSWSMEQLDDTGEPSISYGTDPVAYKAGKRYTLNFNTGVVGPDLKADSSQGARRAGNSMDAYVQLFSDGAGHSGTSPVSGGSTRLESGGRLIAKGAPGAVNAELPAASAPYRLTMEASRPAKDATTSTKVAVAWTFTSAKTPDEPPTDLPLSTVRLAPKLALNGTAPAGGTLTVPLKVAGAAAGRGKVAELTVKVSYDGGRTWKTAPVTTDAAGARTASVRHPATAKAVSYRVYLKDTSGNTMTETISNAYRLAP
>NZ_CP030771.1|WP_138958037.1|1222185_1223037_-|LysR-family-transcriptional-regulator
MELRTLRYFVAVAEELHFGRAAARLHMSQPPLSRAIKQLETGFGAALFVRSSAGVRLTGAGSVLLDEARALLERAEQVHARVAAAAGAATLTVGILGDSADPDAARLAEAFRGRHPHVEVRVRETDLTDPTCGLHAGLVDVALTRGPFDETGLSTRELRADPVGALLRADDPLARGDRLRLADLADRRWFLFPQGTDGVWQTYWSGGEPREGPVVRAVQECRQAVLWNGTVGMTPLGHEPGRGLTVVPLADMEPSRVLVAWNEGDTNPLIRSFVRIAVDSYRY
>NZ_CP030771.1|WP_138958038.1|1223117_1223633_+|cupin-domain-containing-protein
MTETPKTAATPDTGTPDADPAVTVVGPGEGEVIVLGTTRMRVLEDGAATGNRLGCTESVLAPHTPGPPQHRHARHDEGFYVLSGSVRFTVGRQDHDVPAGAFVTVPPGAPHTFANVTGEPAVMLSVFTPSLYVQYFRDLQAAAAEGRSLTPQEHLRTMSRYATEPATDVAP
>NZ_CP030771.1|WP_138958039.1|1223629_1223992_+|DoxX-family-protein
MNVAYGVIAALLALFYLYGGGLKAVRSRERLLPMMAWVDDTPMPVVRSLGAVEVLGALGLVLPPLTGIAPWLGSAAAVGFVALQLAAIRVHLRRGDRAVALNVTLLLAAAATAGLSTAWW

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_4

2554386-2554494

Orphan

Consensus_repeat	Method
GGTTGAGGCTCAACCATGAGGTGCCCAGGAACGGGCGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_4

>merge|NZ_CP030771|4|2554386-2554494|CRISPRCasFinder
GGTTGAGGCTCAACCATGAGGTGCCCAGGAACGGGCGGGCGGGCGGGAAAGAAACGCCGCGGAGCGGCGCGGTTGAGGCTCAACCATGAGGTGCCCAGGAATGGGCGGG

>NZ_CP030771|4|3|2554386-2554494|CRISPRCasFinder
GGTTGAGGCTCAACCATGAGGTGCCCAGGAACGGGCGGG	CGGGCGGGAAAGAAACGCCGCGGAGCGGCGC
GGTTGAGGCTCAACCATGAGGTGCCCAGGAATGGGCGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138959027.1\|2563786_2564848_-\|alkene-reductase	unknown	unknown	gnl\|CDD\|239243
NZ_CP030771.1\|WP_138959021.1\|2555920_2557009_-\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|238624
NZ_CP030771.1\|WP_138959024.1\|2559235_2560507_+\|diaminobutyrate--2-oxoglutarate-transaminase	unknown	unknown	gnl\|CDD\|236437
NZ_CP030771.1\|WP_138959017.1\|2550298_2551651_+\|cobyrinate-a,c-diamide-synthase	unknown	unknown	gnl\|CDD\|234896
NZ_CP030771.1\|WP_138959011.1\|2542133_2542871_+\|hydrolase	unknown	unknown	gnl\|CDD\|119374
NZ_CP030771.1\|WP_138959023.1\|2558596_2559154_+\|diaminobutyrate-acetyltransferase	unknown	unknown	gnl\|CDD\|131459
NZ_CP030771.1\|WP_138959018.1\|2551695_2552424_-\|ZIP-family-metal-transporter	unknown	unknown	gnl\|CDD\|223505
NZ_CP030771.1\|WP_138959016.1\|2549696_2550305_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	unknown	unknown	gnl\|CDD\|235662
NZ_CP030771.1\|WP_138959014.1\|2544991_2545951_+\|cobalamin-biosynthesis-protein	unknown	unknown	gnl\|CDD\|234919
NZ_CP030771.1\|WP_138959028.1\|2565036_2565531_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224759
NZ_CP030771.1\|WP_138959019.1\|2552556_2554191_+\|threonine-phosphate-decarboxylase	unknown	unknown	gnl\|CDD\|236128
NZ_CP030771.1\|WP_138959013.1\|2544363_2544591_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138959012.1\|2543085_2544351_+\|inorganic-phosphate-transporter	unknown	unknown	gnl\|CDD\|376541
NZ_CP030771.1\|WP_138959022.1\|2557107_2558211_+\|aminotransferase-class-V-fold-PLP-dependent-enzyme	unknown	unknown	gnl\|CDD\|223153
NZ_CP030771.1\|WP_138959020.1\|2554640_2555564_-\|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138958190.1\|2562064_2563735_+\|IS1182-family-transposase	unknown	unknown	gnl\|CDD\|372705
NZ_CP030771.1\|WP_138959026.1\|2561031_2561931_+\|ectoine-hydroxylase	unknown	unknown	gnl\|CDD\|131461
NZ_CP030771.1\|WP_138966319.1\|2545947_2547507_+\|cobyric-acid-synthase	unknown	unknown	gnl\|CDD\|234838
NZ_CP030771.1\|WP_138959025.1\|2560563_2560968_+\|ectoine-synthase	unknown	unknown	gnl\|CDD\|183953
NZ_CP030771.1\|WP_138959015.1\|2547687_2549697_+\|putative-cobaltochelatase	unknown	unknown	gnl\|CDD\|274135

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138959027.1\|2563786_2564848_-\|alkene-reductase	gnl\|CDD\|239243	cd02933, OYE_like_FMN, Old yellow enzyme (OYE)-like FMN binding domain. OYE was the first flavin-dependent enzyme identified, however its true physiological role remains elusive to this day. Each monomer of OYE contains FMN as a non-covalently bound cofactor, uses NADPH as a reducing agent with oxygens, quinones, and alpha,beta-unsaturated aldehydes and ketones, and can act as electron acceptors in the catalytic reaction. Members of OYE family include 12-oxophytodienoate reductase, pentaerythritol tetranitrate reductase, morphinone reductase, and related enzymes.	0
NZ_CP030771.1\|WP_138966319.1\|2545947_2547507_+\|cobyric-acid-synthase	gnl\|CDD\|234838	PRK00784, PRK00784, cobyric acid synthase.	0
NZ_CP030771.1\|WP_138959024.1\|2559235_2560507_+\|diaminobutyrate--2-oxoglutarate-transaminase	gnl\|CDD\|236437	PRK09264, PRK09264, diaminobutyrate--2-oxoglutarate transaminase.	0
NZ_CP030771.1\|WP_138959017.1\|2550298_2551651_+\|cobyrinate-a,c-diamide-synthase	gnl\|CDD\|234896	PRK01077, PRK01077, cobyrinate a,c-diamide synthase.	0
NZ_CP030771.1\|WP_138959014.1\|2544991_2545951_+\|cobalamin-biosynthesis-protein	gnl\|CDD\|234919	PRK01209, cobD, cobalamin biosynthesis protein.	1.859e-117
NZ_CP030771.1\|WP_138959023.1\|2558596_2559154_+\|diaminobutyrate-acetyltransferase	gnl\|CDD\|131459	TIGR02406, L-24-diaminobutyric_acid_acetyltransferase, diaminobutyrate acetyltransferase. This enzyme family is the EctA of ectoine biosynthesis. Ectoine is a compatible solute, analagous to trehalose, betaines, etc., found often in halotolerant organisms. EctA is L-2,4-diaminobutyric acid acetyltransferase, also called DABA acetyltransferase. [Cellular processes, Adaptations to atypical conditions].	2.40539e-66
NZ_CP030771.1\|WP_138959018.1\|2551695_2552424_-\|ZIP-family-metal-transporter	gnl\|CDD\|223505	COG0428, COG0428, Predicted divalent heavy-metal cations transporter [Inorganic ion transport and metabolism].	1.61242e-12
NZ_CP030771.1\|WP_138959016.1\|2549696_2550305_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	gnl\|CDD\|235662	PRK05986, PRK05986, cob(I)yrinic acid a,c-diamide adenosyltransferase.	3.22797e-106
NZ_CP030771.1\|WP_138959028.1\|2565036_2565531_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.054e-21
NZ_CP030771.1\|WP_138959019.1\|2552556_2554191_+\|threonine-phosphate-decarboxylase	gnl\|CDD\|236128	PRK07908, PRK07908, threonine-phosphate decarboxylase.	1.00733e-147
NZ_CP030771.1\|WP_138959011.1\|2542133_2542871_+\|hydrolase	gnl\|CDD\|119374	cd06412, GH25_CH-type, CH-type (Chalaropsis-type) lysozymes represent one of four functionally-defined classes of peptidoglycan hydrolases (also referred to as endo-N-acetylmuramidases) that cleave bacterial cell wall peptidoglycans. CH-type lysozymes exhibit both lysozyme (acetylmuramidase) and diacetylmuramidase activity. The first member of this family to be described was a muramidase from the fungus Chalaropsis. However, a majority of the CH-type lysozymes are found in bacteriophages and Gram-positive bacteria such as Streptomyces and Clostridium. CH-type lysozymes have a single glycosyl hydrolase family 25 (GH25) domain with an unusual beta/alpha-barrel fold in which the last strand of the barrel is antiparallel to strands beta7 and beta1. Most CH-type lysozymes appear to lack the cell wall-binding domain found in other GH25 muramidases.	2.90146e-110
NZ_CP030771.1\|WP_138959012.1\|2543085_2544351_+\|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.	2.77232e-95
NZ_CP030771.1\|WP_138959022.1\|2557107_2558211_+\|aminotransferase-class-V-fold-PLP-dependent-enzyme	gnl\|CDD\|223153	COG0075, COG0075, Serine-pyruvate aminotransferase/archaeal aspartate aminotransferase [Amino acid transport and metabolism].	2.13833e-78
NZ_CP030771.1\|WP_138958190.1\|2562064_2563735_+\|IS1182-family-transposase	gnl\|CDD\|372705	pfam13751, DDE_Tnp_1_6, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis.	1.33432e-30
NZ_CP030771.1\|WP_138959026.1\|2561031_2561931_+\|ectoine-hydroxylase	gnl\|CDD\|131461	TIGR02408, putative_L-proline_4-hydroxylase, ectoine hydroxylase. Both ectoine and hydroxyectoine are compatible solvents that serve as protectants against osmotic and thermal stresses. A number of genomes synthesize ectoine. This enzyme allows conversion of ectoine to hydroxyectoine, which may be more effective for some purposes, and is found in a subset of ectoine-producing organisms.	2.4344e-170
NZ_CP030771.1\|WP_138959021.1\|2555920_2557009_-\|amidohydrolase-family-protein	gnl\|CDD\|238624	cd01299, Met_dep_hydrolase_A, Metallo-dependent hydrolases, subgroup A is part of the superfamily of metallo-dependent hydrolases, a large group of proteins that show conservation in their 3-dimensional fold (TIM barrel) and in details of their active site. The vast majority of the members have a conserved metal binding site, involving four histidines and one aspartic acid residue. In the common reaction mechanism, the metal ion (or ions) deprotonate a water molecule for a nucleophilic attack on the substrate. The function of this subgroup is unknown.	4.26135e-61
NZ_CP030771.1\|WP_138959025.1\|2560563_2560968_+\|ectoine-synthase	gnl\|CDD\|183953	PRK13290, ectC, L-ectoine synthase; Reviewed.	5.18474e-77
NZ_CP030771.1\|WP_138959015.1\|2547687_2549697_+\|putative-cobaltochelatase	gnl\|CDD\|274135	TIGR02442, Uncharacterized_protein_Rv2850c/MT2916, cobaltochelatase subunit. Cobaltochelatase is responsible for the insertion of cobalt into the corrin ring of coenzyme B12 during its biosynthesis. Two versions have been well described. CbiK/CbiX is a monomeric, anaerobic version which acts early in the biosynthesis (pfam06180). CobNST is a trimeric, ATP-dependent, aerobic version which acts late in the biosynthesis (TIGR02257/TIGR01650/TIGR01651). A number of genomes (actinobacteria, cyanobacteria, betaproteobacteria and pseudomonads) which apparently biosynthesize B12, encode a cobN gene but are demonstrably lacking cobS and cobT. These genomes do, however contain a homolog (modelled here) of the magnesium chelatase subunits BchI/BchD family. Aside from the cyanobacteria (which have a separate magnesium chelatase trimer), these species do not make chlorins, so do not have any use for a magnesium chelatase. Furthermore, in nearly all cases the members of this family are proximal to either CobN itself or other genes involved in cobalt transport or B12 biosynthesis.	0

>NZ_CP030771.1|WP_138959019.1|2552556_2554191_+|threonine-phosphate-decarboxylase
MADRPADRAPAPGDRAPAPRPPAVVVGVGAGRGVPADEVLGLVRECLRDAGLSPLSVRELATVDAKGDEPGVVGAAARLGVPLVTYPAPELARVAVPNPSGAPLAAAGTPSVAEAAALARGGELLVAKRKSARATCAVARARPEPGPAPPPTPPFTPPPPPSPSPSPSSIPTPTPTPTKGTVITAMDLSTDTTAAGAAGGDVDLRHHGDAEVRGRDDLVDLAVNVRSDTPPSWLKQHIAASLDGLAAYPDGRAARAAVAARHGVEPERVLLTAGAAEAFVLLARALPVRRPVVVHPQFTEPEAALRDAGHTVERVLLRAADGFRLDPAAVPGDADLVVVGNPTNPTSVLHPAEGLARLARPGRVLVVDEAFMDAVPGEREALAGRVDVPGLVVLRSLTKTWGLAGLRIGYVIAAPETIRALERAQPLWPVSSPALAAAEACVAPRALAEAGHVAHRVAAERQHLVAGLRALPGVEVVGPAEGPFVLVRLAGAATVVRERLREGGFMVRRGDTFPGLGPDWMRVAVRDRPTTEAFLRALPEARPR
>NZ_CP030771.1|WP_138959018.1|2551695_2552424_-|ZIP-family-metal-transporter
MAVFVALGAFVMTLVGGWTAGRVTDRRHLVLGLAGGLMLGVVGLDLLPEALEAAGGPVFGVPAALLLAVAGFLLAHVVERLLALRQAAHGGEEHDGRVPEVGLTAAAAMVGHSVMDGVAIGAAFQVGGGMGAAVALAVIAHDFADGFNTYTITKLYGNARRRAVAMLFADAVAPVVGAASTLLFTIPEQLLGGYLGFFGGALLYLAAAEILPEAHHDHPARSTLLCTVAGAGFIWLVVGLAE
>NZ_CP030771.1|WP_138959017.1|2550298_2551651_+|cobyrinate-a,c-diamide-synthase
MVARVVIAAPSSGSGKTTVATGLMAAFTEAGLAVSPHKVGPDYIDPGYHALATGRPGRNLDAYLCGPDLVGPLFAHGSAGCDLAVVEGVMGMFDGAAGQGELASTAHVAKLLRAPVVLVVDASSQSRSVAALVHGFASWDPEVRLGGVILNKVGSARHEELLREALDSSGVPVLGALRRAPQVRAPSRHLGLVPVAERQAEAVASVAALAEQVRQGCDLEGILALARSAGVWSGDAWDPGAGAVPDRPAGRPVVAVAGGAAFTFSYAEHAELLTAAGADVVGFDPLRDERLPEGTAGLVIGGGFPEVYAPELSANEPLRKAVAGLAESGAPVAAECAGLLYLTRELDGKPMCGVLDARARMAERLTLGYREAVAVSDSVLAPAGTRTRGHEFHRTVVEPGAGPAPAWGLHAPERRVEGFVQRGVHASYLHTHWAAEPGIARRFVERCAAG
>NZ_CP030771.1|WP_138959016.1|2549696_2550305_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase
MPKGQPNVVPEDGLTTRQRRNRPLVMVHTGVGKGKSTAAFGMALRAWNQGWPVGVFQFVKSAKWKVGEENALKVLGASGEGGRVDWHKMGEGWSWIQREPAAGEPSHEEKAREGWEQVKRDLAAETYKFYVLDEFAYLLHWGWVDVDEVVAVLRDRPGTQHVVITGRNAPEKLVGYADLVTDMSKVKHPMDAGQKGQRGIEW
>NZ_CP030771.1|WP_138959015.1|2547687_2549697_+|putative-cobaltochelatase
MSTPYPFTAVVGQDDLRLALLLNAVSPQVGGVLVRGEKGTAKSTAVRALSALLPEVSIVADCRFSCDPVAPDPACPDGPHEPGTGAARAARMVELPVGASEDRLVGSLDIERALAEGVKAFEPGLLASANRGILYVDEVNLLHDHLIDLLLDAAAMGASYVEREGVSVRHAARFLLVGTMNPEEGELRPQLLDRFGLTVEVAASREPDQRVEVVKRRLAYDDDPEGFAGRWAEDEAAVRARIVAARALLPRVRLGDGVLRQIAATCAAFEVDGMRADIVMARTATALAAWAGREDVLAEDVRQAALLALPHRRRRNPFDAPGLDEDKLDETLDEFGDDHDGGDDDPGPDGGGGGGVPPQDQGPDAPADGGAPAPGEASDGGQPQGTGAAEQQPVRAAEPFRTKVLSVPGLGDGAAGRRSRARTEHGRTTGSRRPRGTLTKLHLAATVQAAAPHQRARGRAGRGLVVRRDDLRQATREGREGNLVLFVVDASGSMAARKRMGAVKGAVLSLLLDAYQRRDKVGLVTFRGSAADVALPPTSSVDAAAARLESLPTGGRTPLATGLLKAHEVLRIERLRDPARRPLVVVVTDGRATGGPEPVALAGRAARLFAAEGVASVVVDCEAGPVRLGLAGQLAGELGGTAVTLDELRADSIAGLVRNVRAGNERKVA
>NZ_CP030771.1|WP_138966319.1|2545947_2547507_+|cobyric-acid-synthase
MSGGLLVAGTTSDAGKSVVTAGICRWLSRKGVSVAPFKAQNMSLNSFVTREGAEIGRAQAMQAQAARVEPSVLMNPVLLKPGGEKSSQVVLMGKPVGEMSARGYHEYRGGAERSEQGWRRETGGRQQALLDTVVGCLEELRGTYDAVICEGAGSPAEINLRRTDIVNMGIARAARFPVVVVGDIDRGGVFASFFGTVALLGPADQELVAGFLVNKFRGDVSLLEPGLDMLRGLTGRDTFGVLPFRHGLGIDEEDGLRVSLRGAVRESAVAPPLGEDVLRVAVCAVPLMSNFTDVDALAAEPGVVVRFVDRAEELADADLVVVPGTRGTVQALAWLRERGLADALARRAAEGRPVLGICGGFQVLGERIEDDVESRAGSVDGLGLLPVRVRFAREKTLARPVGQALGEPVEGYEIHHGVAEVLGGEPFLDGCRVGEVWGTHWHGSLESDAFRRRFLTEVARAAGRRFVPAPDTSFGALREEQLDLLGDLIEESADTDALLELIENGAPENLPFVPPGAPA
>NZ_CP030771.1|WP_138959014.1|2544991_2545951_+|cobalamin-biosynthesis-protein
MRAADRDFAYGAAAGLLGDLLLGDPRRGHPVAAFGRAAGAVERVLWRDHRGSGVLHTVVCAGGAVAVGALASRAARRSRAASVGLTAAATWAVVGGTSLGREARAIGGALAAGDVDVARERLPHLCGRDPEALDADGIARAVVESVAENTSDAVVGALVWGAVAGVPGLVGFRAVNTLDAMVGHRSARYLRYGWASARLDDVAGWPGARLTGLLAVAAGGAPRRALRAWRSDARLHPSPNAGVVEASFAGALGVRLGGTLSYAGRVEERPVLNEEGRSVVVDDIERAVRLSRRVSWLALGVSVGTHLVRARGRKKGWAL
>NZ_CP030771.1|WP_138959013.1|2544363_2544591_+|hypothetical-protein
MKIDWAALGSVFGVSLVVTVALVGLFTLGIVGLSKQEQARTAGGGGAALAPRVGAYACFALCAAAVAYGIYLIVA
>NZ_CP030771.1|WP_138959012.1|2543085_2544351_+|inorganic-phosphate-transporter
MENITLLLGIVIVTALVFDFTNGFHDTANAMATTISTGALKPKTAVAMSAVLNLVGAFLSVEVAKTISGGIINEDGLKTEVIFAALVGAILWNLLTWLLGLPSSSSHALFGGLIGAAVMSMGWSSVNGGTVVTKVLLPAIAAPLVAGIAASLATRLTYRISSRTDEKATSKGYRAGQIASAGLVSLAHGTNDAQKTMGIITLALITGGVLNPGANPPMWVIVSAGIAIALGTYLGGWRIIRTMGKGLTELAPPQGFAAQTSAATAILASSHIGFSLSTTQVCSGAVMGAGLGRKGGVVRWSTATRMFVAWGLTLPAAGLVGAGAELLTKQGDWGVAATAALLIGGSAVIWSLSRREPVDHTNVTADEIGGSARDTEPAGVVTTAIAAVTPPPAGPLTAAAVAVEPSENTAPVADPARPATV
>NZ_CP030771.1|WP_138959011.1|2542133_2542871_+|hydrolase
MARAHTPSRRRAHALAASVAALAIGGTVLTEVPASAAGEPRGHDVSSHQKNVDWPGAKAKGARFVYVKATESHTYRNPYFRQQYDGSRAAGLLRGAYHFALPNRSSGATQAAYFLRNGGQWTADGWTLPPALDIEHNPYGDRKCYGLSKARMVAWIKAFSDEVRRRSGRTPVIYTTTKWWNDCTGASRAFGGHPLWLARWSAAPEPLPSGWSSWTFWQYADRGPLPGDQNLFGGSTAQLKRFARG
>NZ_CP030771.1|WP_138959020.1|2554640_2555564_-|LPXTG-cell-wall-anchor-domain-containing-protein
MTSNAFRRLPTRRIGALAAATVVAAGPAALGTAGTAHATDDRRGGRAGAVVLRTGLEVSLLNKTVRAPLNVTLNEVSAPASASRTTLTAKLDGVEGGQPFSVLRADVATARATVKGGTAQGYSNVARAKVHVPGLPLLPLVEVDQVTSKAVCTAGKRPVASSTFLGGVTVLGKKVSVKSAGTTQVSVPGVGEVRLDLSSTRTTSRTAAATALRLQVSVDPLKLGVAAVKGAVTLAGATCEAPGPGAKPLPEPQGGKPAEPVSARREAPKQTEDLAETGGSSMTPYVAGGAVVLLLAGGGVLAYTRRR
>NZ_CP030771.1|WP_138959021.1|2555920_2557009_-|amidohydrolase-family-protein
MSDHAVLHVKGRVLVGPEDVRDELWVVGGRVTFERPAARDAVTVQGWALPGLVDAHCHVGLDAHGAVPAEEAEKQALTERDAGALLLRDAGSPSDTRWIDDREDLPKIIRAGRHIARTRRYIRNYAHEVEPGDLAAYVAREARRGDGWVKLVGDWIDREAGDLTACWPRGAVREAIAEAHRLGARVTAHCFAEDSLRDLVEAGIDCVEHATGLTEDTIPLFAERGVAIVPTLVNIATFPQLAAGGEKKFPRWAAHMRRLHERRYDTVRAAYDAGVPVYAGTDAGGSLAHGLIGGEVAELTKAGIPAVDALAATTWGARAWLGRPGLVEGAPGDLVVYEADPRADVRVLTAPRRVVLDGRVVG
>NZ_CP030771.1|WP_138959022.1|2557107_2558211_+|aminotransferase-class-V-fold-PLP-dependent-enzyme
MTHPLLDLAPLSAAHFAAIEDRVARLLDTRQDVVITQGEALLPLEGCIRGAARPGTTALNVITGPYGQTFGDWLRDCGATVVDLAVPFHTAVTAAQVEEAFAAHPEIDFVSLVHAEAATGNTNPVAEIGEVVRAHGALFMLDAVASVAAEPLLPDAWGVDLCVIGAQKAMGGPAGVSAVSVSERAWDRIAANPQAPRRSYLSLLDWKQRWIDGGRKALLHAPAQLEMLALEACLERIESEGLDALMARHTTAAAATRAGAVALGGGLEPYVHEARDAAPVATTLRAPRGVDAAELVARSLAADPVLPLVTGGGALAKEMIRVNHYGPDATRGVVHASLAALGAAMGELGLAVDLEGARRAVTEAWQA
>NZ_CP030771.1|WP_138959023.1|2558596_2559154_+|diaminobutyrate-acetyltransferase
MTAAQADLPTDLQANFLGMPDGLRLDTPDVADGAAIWRIARDSKVLDLNSSYSYLLWCRDFAATSVVARDADGEPVGFVTGYVRPDAPRTLVVWQAAVDHAHRGRGLAAALLDGLTAKVVGTRGITTVETTITPGNTASERLFSSYARRHGAGVERTVLFDAAHFPAEDGGHDPEVLHVIGPLAP
>NZ_CP030771.1|WP_138959024.1|2559235_2560507_+|diaminobutyrate--2-oxoglutarate-transaminase
MTITPPDLSVFETLESEVRSYCRGWPTVFDRAQGSRMYDEDGHEYLDFFAGAGSLNYGHNNPVLKRALLDYLERDGVTHGLDMSTTAKRAFLESFQNLVLRPRDLPYKVMFPGPTGTNAVESALKLARKVKGRESIVSFTNAFHGMSLGSLAVTGNAFKRAGAGIPLVHGTPMPFDHYLDGKVPDFLWFERLLEDQGSGLNKPAAVIVETVQGEGGINVARAEWLRALEALCRRQDMLLIVDDIQMGCGRTGAFFSFEEAGISPDIVTVSKSISGYGLPMALTLFKPELDVWEPGEHNGTFRGNNPAFVTAAAALQTYWSDGPAMEKQTRARGEQVEQTLVALVDEHRADIVEYRGRGLVWGIEFRDKERATAVARRAFELGLLIETSGPESEVVKLLPALTITADELDEGLRTLTRAVRETA
>NZ_CP030771.1|WP_138959025.1|2560563_2560968_+|ectoine-synthase
MIVRSFKDIEGTDRHVKAKSGTWESKRILLAKERVGFSLHETILYAGTETAMWYANHVEAVVCTRGEAELTDHTNGETYRITPGTMYLLDGHEKHTLRVKEDFHCLCVFNPPVTGREDHDENGVYPLLTEPDPE
>NZ_CP030771.1|WP_138959026.1|2561031_2561931_+|ectoine-hydroxylase
MTTAPERTGDLYPTRGAEEVLVERKDPVVWSAPGTPGPFTDEDLAGFDRDGFLAVEQLLTPDEVGTYHAELERLVNDPAMRADERSVVEPRSQEIRSIFEVHRISEVFARLAADPRVAGRARQILGSDVYVHQSRINVKPGFGASGFYWHSDFETWHAEDGLPNMRTVSVSIALTRNHDTNGGLMIMPGSHRTFLGCAGETPKDNYKKSLQMQDAGTPSDEALTGLAAEYGIKLFTGAAGSATWFDCNAMHGSGDNITPYPRSNVFIVFNSVENAAVEPFAAPVRRPEFIGARDFTPVK
>NZ_CP030771.1|WP_138958190.1|2562064_2563735_+|IS1182-family-transposase
MSMRPIGDGEIPAETVRVAQAAFPKGSLAIRLRDELGVLFRDEQFADLFPSRGKPAWSPGRLALVSVLQFAEGLPDRQAALAVRARIDWKYALGLELTDPGFDYSVLSEFRTRLVEAEAGQQVFDHVLESARKAGMLKAPGRARTDSTHVLAAIRSLNRLEFVIETLRAALNALAAAAPNWLSAHADPAWFDRYATRPEDYWLPSGKAKRTELAEQTGRDGMRLLADVHAAGAPVWLRELPAVQILRRAWVQQYVFDTEGEVRWRDPKECPPGALRLVSPYDTDARASVKRDIKWDGFKVHLTETCDADTSHLITNVLTQDATVQDSTATNLVHDALAARDLLPGEHLLDAGYIDGPRIVTADRQYGITLTGPIRGNTTAQASGPYSQSAFAIDWQSQTVTCPNGKNATQWRDKISDRGAPIIIVRFSPADCRTCPARPECVSSPRAARREITLRPRAEHEAIQQARAAQGTPEWRERYAARNGIEGTLSHAVHTAGLRRCRYRGLARTRLQHQLTATAINLARLDAHLTGTPLARTRTSHFARLRPADQTIDGAK
>NZ_CP030771.1|WP_138959027.1|2563786_2564848_-|alkene-reductase
MTTAFDPIDLAGTPLANRIAMAPMTRSRAAAGGVPTDLNAEYYAQRATAGLVITEGVQPSVVGQGYPDTPGLHSAEQIEGWRKVTDAVHAAGGRIFAQLMHTGRIGHPVLLPDGLVPVGASPIAAEGQVYTHEGPKDYVTPRELTGDEVRATVGEFVTAARNAIEAGFDGVELHGANGYLIHQFLAPGSNRRTDEWGGSVENRVRFAVEVAKAVAAEIGAARTGIRLSPGNPLNGIHEPDPDETYLALVERLSPLGLAYLHVMEVGPIRELVTALRKGFDGPFILNPATEGPTGPGELALIEDGTADLLSYGSLFLANPDLPARLRTGGPFNEPDRATFYGGDAKGYTDYPAL
>NZ_CP030771.1|WP_138959028.1|2565036_2565531_+|MarR-family-transcriptional-regulator
MKTEAERAEPACPSAARGGPVSTSIARVARLHRIAAGKLLKDAGLYPGQELMMMHLWESGAVRQSELIRMVELDPSTVTKMLQRLEQAGHVRRRPDPADRRAVLVEATDDDNGLMRAVESAWTKLEQHTLAGLDPDERAQLGRLLSRVEANLCVETAGCPEVSR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_5

4068731-4068889

Orphan

Consensus_repeat	Method
CCGCGTCGGGGCCGGGCCTCGCGCAGCCGGGGAGGGACGGGTGGGCGGGTGGGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_5

>merge|NZ_CP030771|5|4068731-4068889|CRISPRCasFinder
CCGCGTCGGGGCCGGGCCTCGCGCAGCCGGGGAGGGACGGGTGGGCGGGTGGGAGAACCGCCGCGGTAGCGGCGGAAACGGGGACGGCGCCACGCGCAGGCGCACCGCGTCGGGGCCCGGCCTCGCGCAGCCGGGGAGGGACGGGTGGGCGGGTGGGAG

>NZ_CP030771|5|4|4068731-4068889|CRISPRCasFinder
CCGCGTCGGGGCCGGGCCTCGCGCAGCCGGGGAGGGACGGGTGGGCGGGTGGGAG	AACCGCCGCGGTAGCGGCGGAAACGGGGACGGCGCCACGCGCAGGCGCA
CCGCGTCGGGGCCCGGCCTCGCGCAGCCGGGGAGGGACGGGTGGGCGGGTGGGAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138960089.1\|4069598_4070936_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|367673
NZ_CP030771.1\|WP_138960088.1\|4068920_4069469_-\|acyl-CoA-thioesterase	unknown	unknown	gnl\|CDD\|224523
NZ_CP030771.1\|WP_138960090.1\|4071097_4072219_+\|membrane-dipeptidase	unknown	unknown	gnl\|CDD\|366534
NZ_CP030771.1\|WP_138960096.1\|4077878_4079030_-\|5-(carboxyamino)imidazole-ribonucleotide-synthase	unknown	unknown	gnl\|CDD\|235674
NZ_CP030771.1\|WP_138966583.1\|4065924_4066932_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133016
NZ_CP030771.1\|WP_138960093.1\|4075042_4076026_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP030771.1\|WP_138960091.1\|4072240_4073566_-\|nucleotide-sugar-dehydrogenase	unknown	unknown	gnl\|CDD\|223936
NZ_CP030771.1\|WP_138960079.1\|4054207_4055524_+\|coenzyme-F420-0:L-glutamate-ligase	unknown	unknown	gnl\|CDD\|183957
NZ_CP030771.1\|WP_138960083.1\|4059739_4060492_+\|TIGR03089-family-protein	unknown	unknown	gnl\|CDD\|274426
NZ_CP030771.1\|WP_138960097.1\|4079288_4079819_+\|GtrA-family-protein	unknown	unknown	gnl\|CDD\|377229
NZ_CP030771.1\|WP_138960086.1\|4064114_4065890_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|367673
NZ_CP030771.1\|WP_138960087.1\|4067103_4068651_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|367673
NZ_CP030771.1\|WP_138960085.1\|4062186_4063971_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|367673
NZ_CP030771.1\|WP_138960080.1\|4055663_4056668_-\|DNA-3-methyladenine-glycosylase-2-family-protein	unknown	unknown	gnl\|CDD\|223200
NZ_CP030771.1\|WP_171075757.1\|4060652_4061960_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|367673
NZ_CP030771.1\|WP_138960092.1\|4073786_4074944_+\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|173847
NZ_CP030771.1\|WP_138960094.1\|4076106_4077303_-\|membrane-dipeptidase	unknown	unknown	gnl\|CDD\|366534
NZ_CP030771.1\|WP_138960095.1\|4077342_4077882_-\|5-(carboxyamino)imidazole-ribonucleotide-mutase	unknown	unknown	gnl\|CDD\|376377
NZ_CP030771.1\|WP_138960082.1\|4058071_4059601_-\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|128941
NZ_CP030771.1\|WP_138960081.1\|4056894_4057977_-\|NTP-transferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|224129

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138960089.1\|4069598_4070936_+\|LCP-family-protein	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	1.86108e-55
NZ_CP030771.1\|WP_138960088.1\|4068920_4069469_-\|acyl-CoA-thioesterase	gnl\|CDD\|224523	COG1607, COG1607, Acyl-CoA hydrolase [Lipid metabolism].	1.27552e-49
NZ_CP030771.1\|WP_138960090.1\|4071097_4072219_+\|membrane-dipeptidase	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	3.74348e-98
NZ_CP030771.1\|WP_138960096.1\|4077878_4079030_-\|5-(carboxyamino)imidazole-ribonucleotide-synthase	gnl\|CDD\|235674	PRK06019, PRK06019, phosphoribosylaminoimidazole carboxylase ATPase subunit; Reviewed.	1.82349e-178
NZ_CP030771.1\|WP_138966583.1\|4065924_4066932_-\|glycosyltransferase	gnl\|CDD\|133016	cd02525, Succinoglycan_BP_ExoA, ExoA is involved in the biosynthesis of succinoglycan. Succinoglycan Biosynthesis Protein ExoA catalyzes the formation of a beta-1,3 linkage of the second sugar (glucose) of the succinoglycan with the galactose on the lipid carrie. Succinoglycan is an acidic exopolysaccharide that is important for invasion of the nodules. Succinoglycan is a high-molecular-weight polymer composed of repeating octasaccharide units. These units are synthesized on membrane-bound isoprenoid lipid carriers, beginning with galactose followed by seven glucose molecules, and modified by the addition of acetate, succinate, and pyruvate. ExoA is a membrane protein with a transmembrance domain at c-terminus.	4.40132e-92
NZ_CP030771.1\|WP_138960093.1\|4075042_4076026_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	2.71136e-30
NZ_CP030771.1\|WP_138960091.1\|4072240_4073566_-\|nucleotide-sugar-dehydrogenase	gnl\|CDD\|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0
NZ_CP030771.1\|WP_138960079.1\|4054207_4055524_+\|coenzyme-F420-0:L-glutamate-ligase	gnl\|CDD\|183957	PRK13294, PRK13294, F420-0--gamma-glutamyl ligase; Provisional.	0
NZ_CP030771.1\|WP_138960083.1\|4059739_4060492_+\|TIGR03089-family-protein	gnl\|CDD\|274426	TIGR03089, conserved_hypothetical_protein, TIGR03089 family protein. This protein family is found, so far, only in the Actinobacteria (Streptomyces, Mycobacterium, Corynebacterium, Nocardia, Propionibacterium, etc.) and never more than one to a genome. Members show twilight-level sequence similarity to family of AMP-binding enzymes described by pfam00501.	1.71847e-73
NZ_CP030771.1\|WP_138960097.1\|4079288_4079819_+\|GtrA-family-protein	gnl\|CDD\|377229	pfam04138, GtrA, GtrA-like protein. Members of this family are predicted to be integral membrane proteins with three or four transmembrane spans. They are involved in the synthesis of cell surface polysaccharides. The GtrA family are a subset of this family. GtrA is predicted to be an integral membrane protein with 4 transmembrane spans. It is involved is in O antigen modification by Shigella flexneri bacteriophage X (SfX), but does not determine the specificity of glucosylation. Its function remains unknown, but it may play a role in translocation of undecaprenyl phosphate linked glucose (UndP-Glc) across the cytoplasmic membrane. Another member of this family is a DTDP-glucose-4-keto-6-deoxy-D-glucose reductase, which catalyzes the conversion of dTDP-4-keto-6-deoxy-D-glucose to dTDP-D-fucose, which is involved in the biosynthesis of the serotype-specific polysaccharide antigen of Actinobacillus actinomycetemcomitans Y4 (serotype b). This family also includes the teichoic acid glycosylation protein, GtcA, which is a serotype-specific protein in some Listeria innocua and monocytogenes strains. Its exact function is not known, but it is essential for decoration of cell wall teichoic acids with glucose and galactose.	4.97677e-24
NZ_CP030771.1\|WP_138960086.1\|4064114_4065890_+\|LCP-family-protein	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	3.80296e-46
NZ_CP030771.1\|WP_138960087.1\|4067103_4068651_+\|LCP-family-protein	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	2.05054e-55
NZ_CP030771.1\|WP_138960085.1\|4062186_4063971_+\|LCP-family-protein	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	6.09966e-51
NZ_CP030771.1\|WP_138960080.1\|4055663_4056668_-\|DNA-3-methyladenine-glycosylase-2-family-protein	gnl\|CDD\|223200	COG0122, AlkA, 3-methyladenine DNA glycosylase/8-oxoguanine DNA glycosylase [DNA replication, recombination, and repair].	8.99736e-27
NZ_CP030771.1\|WP_171075757.1\|4060652_4061960_+\|LCP-family-protein	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	1.0013e-57
NZ_CP030771.1\|WP_138960092.1\|4073786_4074944_+\|acyl-CoA-dehydrogenase-family-protein	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.	0
NZ_CP030771.1\|WP_138960094.1\|4076106_4077303_-\|membrane-dipeptidase	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	1.19903e-143
NZ_CP030771.1\|WP_138960095.1\|4077342_4077882_-\|5-(carboxyamino)imidazole-ribonucleotide-mutase	gnl\|CDD\|376377	pfam00731, AIRC, AIR carboxylase. Members of this family catalyze the decarboxylation of 1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (AIR). This family catalyze the sixth step of de novo purine biosynthesis. Some members of this family contain two copies of this domain.	2.18282e-89
NZ_CP030771.1\|WP_138960082.1\|4058071_4059601_-\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|128941	smart00701, PGRP, Animal peptidoglycan recognition proteins homologous to Bacteriophage T3 lysozyme. The bacteriophage molecule, but not its moth homologue, has been shown to have N-acetylmuramoyl-L-alanine amidase activity. One member of this family, Tag7, is a cytokine.	2.41103e-48
NZ_CP030771.1\|WP_138960081.1\|4056894_4057977_-\|NTP-transferase-domain-containing-protein	gnl\|CDD\|224129	COG1208, GCD1, Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis/translation initiation factor 2B, gamma/epsilon subunits (eIF-2Bgamma/eIF-2Bepsilon) [Cell envelope biogenesis, outer membrane / Translation, ribosomal structure and biogenesis].	1.99815e-100

>NZ_CP030771.1|WP_138960087.1|4067103_4068651_+|LCP-family-protein
MGLRFWRPPAHAATAEVSSHVPAPHRSPAPPPRRPHPPRPPRPPARPAARRTRRPRWAMRIATALSVTVLGAAGIGHSVVSSLDTGIRRVDAFKDMKNRPEGSHGTNVLLVGTDGRDRISRAEKRKYRLGGAPCHCTDTIMIVHISEDRERASVVSLPRDSYAELPPHVDQNSRKHHRSHPVKINAAYAEGGPNLTVRTVERMTKVKIDHYLEVDFTSFMKTVDVVGGVEICTAIPLKDSYTGLDLSVGTHQLSGGQALQYVRSRHIDGAADLGRMQRQQRFLAALIAKATSSGVLLNPVKFRDVSKTLLGSVRADDGFGTTDMLALGRAMRNFSPSSSEFTTVPLAPKGQLIPGVGSTLKWDPQKSAKLFQALRDDKPLAPHRERRKAALVPVSPGQIRVQVDNGTRTSGLGRRVDSALRKSGFRTSGVPGSVPLAPGAGPLARTVVAYDPRWDRSAKSLATALPGCEMRRVNGQGPTLKVLAGADFRGVRAVRAEDAHQGEFGAITGDQVICP
>NZ_CP030771.1|WP_138966583.1|4065924_4066932_-|glycosyltransferase
MIMPVLNEERHLREAVHAILKQEYAGEMEVVVALGPSTDRTDEIAAELVAEDPRVHTVPNPTGRTPAALNAAIKASRHPIVVRVDGHAALSPGYITTAVRLLEETGAMNVGGIMHAEGENDWEHAVAAAMTSKIGVGNAAFHTGGDAQQAETVYLGVFRREALEQQGGYNEEFIRAQDWELNFRIREAGGLIWFSPELKVSYRPRPSVKALAKQYKDYGRWRHVVARYHEGSINLRYLAPPTAVCAIAAGLVVGAALTPWGLVIPGGYLAAIAAGSVPAGKGLPLKARLQIPVALATMHMSWGWGFLTSPRSLAKKVIASRRPAVLGTDRKPQEA
>NZ_CP030771.1|WP_138960086.1|4064114_4065890_+|LCP-family-protein
MGQNSVRGEGVSSGAGTHEATSERSRAEGDRPDSDAKDAEPHARDTAEPHARDTKAPGPSRGTAGGGRSRGKGDAEGEGRSRRKEARGSRSRTRRAAPRRKRRVLRWSATVLAVLILGTAGAGYLYYQHLNSNLETDDLNLGDHRAPAPTPNAAGQTPLNILLIGSDARDSKANQKLGGAKDTFGGPPLADVQMLLHLSADRTNMSMVSMPRDTLLTIPKCTDPDDGKVYDELGPRAMTNESLGRGGPGCTVATWEKLTNIRIDHFMMVDFSGVVSMADAIGGVPVCVDKNIHSRTRAGKGSGLKLPKGTSKIQGEQALQWLRTRYGFEDGSDIGRAKAQHMYMNSLVRTLRDNASLTSPNRLRKLAENATKALKVDPGLGSVLKLYDLGNELKKVSPERTTMTTMPFEYSGSRVVPKPGDAEQLFRLVRDDIPLDGKGKKKKPKEKPSDDPAAPDADIAVQVQNGTRTATEPPVSGRASTVAQLLAAAGFSKAAPDTATALTEARTVVRYPSVDLEGDAQRVAKSLGLPLSAAKRSTDVSGVTLVVGADWREGDKPEKAKRQDDSTPKSADALNGSDKKACMKVDPNFTW
>NZ_CP030771.1|WP_138960085.1|4062186_4063971_+|LCP-family-protein
MDAQGRGRAENIDPADQWVLNPQTGDYELRLSPSAEQSAPQTGVPGPRRGAPRRGAPRPADPQQSTPQQGAPRPGTRGPERPGGREQQVPGQRRRRAAQPEAAGSRRKGKTKKKKSTGKRILAWTGGTVAFVIVAAGVGGYLYYQHLNDNITAVSDDGAGTGGFSKDRAINILLVGTDERSGDGNKGYGDEGSVGHADTTILLHVSKDRSNATALSIPRDLITDIPDCPTKQDDGSTKTIPGSQKVRFNESLGQNERTPSCVMRTVTQITGIELDHFMVADFNAVKTLSSAVDGVDVCLAKDFDDPKSHLKLPAGKHSIEGEEALAFVRTRYTVGTGGDLSRIQLQQQFLSSLMRKLKSKGTLTSPTKIISLAEAGTKALTVDSKIKDILKLRDLGMELGKFDMKNLTFATTPVIDNPAEKKPVTVVLNKAKSDELFSMLREDVSLTEVKKKEKKEKAAVAARLKGPRAEAADVRVDVYNGSDRNGAAQETLSWLQNTEGVTKSSQLGNAGKQGKTTVEYSAGQADEARKLADLMGLPAAALKPGKSEKNAQGLPAIVLTLGADFKGAGVPVKAPSKAPDGIQKVEADKTVCAK
>NZ_CP030771.1|WP_171075757.1|4060652_4061960_+|LCP-family-protein
MTDSTYGPGAGASPSGLAARRRRRRWLRYAGVGTAVVVLAAGGVGWAVYQKLDGNITEDTDAAAELARYEKERPTPLVHDAQNILLIGSDTRSGRGNHKYGRDLGTQRSDTTILLHLAADRQSATAVSLPRDLMVRIPSCRRPDGSRTRAQFAQFNWAFEFGGTACTIRTVEKLTNIRVDHHMVVDFAGFKDMVDAVDGVQVCLKAPVDDAAAKLRLPAGRQTLNGEQALGFVRARKSLGNGSDTERMDRQQEFLGALVNKVRSNDVLLNPVKLYPVLDAATSSLTTDPGLASLRGLYELVRGLRNIPTERVQFLTVPRRSYTYDANRDELVEPAADELFTRLRTDEPVQVTRARPDVSNASATSNSDGSSYENGDDGGEYEEEDDSGDGADEYTDSGDYEDGGEWSDEKPDDPTHTPSPAPTFRGNTAAGSTCA
>NZ_CP030771.1|WP_138960083.1|4059739_4060492_+|TIGR03089-family-protein
MNANDRTPADLLRSALAADPARPLVTYYDDATGERVELSVATFANWVAKTANLLQGDLAAEPGDRLALLLPAHWQTAVWLLACSSVGVVADVGGDPAGADLVVSGPDTLEAARACSGERVALALRPLGGRFPEAPDGFADYAVEVPSQGDRFAPYAPVDPDGPALAVGGAELTGAEVVARALDDAAGLGLAAGARLLSGRPYDSWDGLSAGLYAPLASGGSVVLCRHLDRAPEGGLEKRVEAERVTVTVR
>NZ_CP030771.1|WP_138960082.1|4058071_4059601_-|N-acetylmuramoyl-L-alanine-amidase
MRGFLASSIGVTCAAALALPVALPSTAAATAAGPPAAGALPGSTQSLPLAPLGSDRAGGGPRAEGLPRRDVRPFSLLGVVWDDADAELRGTVQVRTRATGTTVWSAWQDVETHNHEHAADPGAAERGSGRVRGATAPLWVGDSDGVEVRVRARGAEPATGARAGRPDTARDRAPASHAHASTADAEGRAPAGDGGGRTSADGVEGRTPTDGVEGRTSADGAPADGSPGLLPAGLRLELVDPGAEPPPGGAPADAPRATTLTAEAAASSAVNADLAPLGALAVPELTKERTRADLLAARGLPGATGARPYVGPRPRIVTRRGWGADERLRERNFAYTKTVKAAFVHHSATGNNYRCSQAPSVLRSIYRYHVESSGWRDIGYNFAVDKCGNIYEGRAGGVAKAVLGAHTLGFNTNSMGIAVLGTYTSAAPPKAAVTAVARLTAWKLGLFGANPRGTTYLKSGGGNLYSKGTKVRLHVISGHRDGFATECPGRRLYSKLGTARTASARYQGR
>NZ_CP030771.1|WP_138960081.1|4056894_4057977_-|NTP-transferase-domain-containing-protein
MTEAILLVGGKGTRLRPLTVNTPKPMVPAAGVPFLTHQLARARAAGVDHIVLATSYLAEVFEPYFGDGSAFGLHIEYVTEEEPLGTGGALRNVASRLRSGPQDPVLVFNGDILTGLDIRALVAEHERTRADVSLHLTRVTDPRAYGLVPTDGTGKVLAFLEKPQTPEEIVTDQINAGAYVFRRSVIDTIPAGRPVSVERETFPELLASGAHLQGLVDSTYWLDLGTPQAFVRGSADLVLGRAPSPAVPGRCGDRLVLPSARVASDAKLTGGTVIGEHAVVGEGARLYGSTILSGAVIEPGAVITDSLIGARASVGARSVLTGAVVGDGARIGADNELRDGVRVWCEATLPAGAVRFSSDQ
>NZ_CP030771.1|WP_138960080.1|4055663_4056668_-|DNA-3-methyladenine-glycosylase-2-family-protein
MSSRFAPRPTRTTVRGGETRVPVASPRPATAAMRRTWTPEAPLHLGLTLGPLRRGPADPTFRTTPDGSVWRATRTPQGPATLRVALRAGTAEAEAWGPGADWALDTLPDLLGAADAPDGFTASHRLVAHTERRRQGLRLTRTGLVLESLIPSVLEQKVTTDEAYRAWRLLVRAYGEPAPGPTPPQARMHVMPDPETWRRIPSWEWHRAGVDDKRASAILRAARVAARLEEAAAMPVEEARARLELVPGIGPWTSAETVQRSNGAPDAVTVGDLHLPGIIGYALAGERDADDARMLELLAPYAGQRHRAARLICLSGHTPPRRKPKMPKADIAAL
>NZ_CP030771.1|WP_138960079.1|4054207_4055524_+|coenzyme-F420-0:L-glutamate-ligase
MTAPAFRAWAVPGLPEVREGDDLAKLIATAEPGLADGDVVLVTSKVVSKAEGRVVAAADREAAIDAETVRVVARRGTLRIVENRQGLVMAAAGVDASNTPAGTVLLLPEDPDASARALREGLRDALGVDVGVLVTDTFGRPWRSGLTDVAIGAAGVRVLDDLRGGVDSYGNPLQATVVATADELAAAGDLVKGKAAGLPVAVVRGLPHAVRGADTPDDTDTGARALVRDARDDMFRLGTSEAVREALALRRTVREFTDEPVDPGAVRRAVAAAVTAPAPHHTTPWRFVLLESAESRLRLLDAMREAWIADLRRDGKSEESIARRVRRGDVLRNAPYLVVPCLVTDGAHTYGDERRDTAEREMFVVAAGAGVQNLLVALAGERLGSAWVSSTMFCRDVVRDVLGLPPEWEPMGAVAVGHPAGAPGARVGRDAEEFLVVR
>NZ_CP030771.1|WP_138960088.1|4068920_4069469_-|acyl-CoA-thioesterase
MTDQATAPEPEIPGKPTSVSRTTLSHIMTHADTNLLGTVHGGVIMKLVDDAAGAVAGRHSGGPAVTASMDEMAFLSPVRVGDLVHVKAQVNWTGRTSMEVGVRVLAERWNESTPAQQVGSAYLVFAAVDADGKPRLVPPVEPETDRDRRRYQEAQIRRTHRLARRRAIKDLREARAREGYED
>NZ_CP030771.1|WP_138960089.1|4069598_4070936_+|LCP-family-protein
MSDWPDARNGNNGDRHGYGSGNAQPEGARVMRHVQRPDGVPRQPSYDDNVYDDLYRDQRAQPGQQHGQQHAQGPGGPEGYDSGYNTGQVYGSPGGPRRGQAPGGPQGPGGPPAPPRPKPPVNWKKRITWGLVTFLALLIVVSVSTYFWADSKLKREVDLSKVIERPAGGKGTNYLIVGSDSRAGMSDEEKKKLHTGSAEGKRTDSMMILHVADDGGNTMVSLPRDSNVTIPSFKGAESGKLYPATGRQTKLNAAYAEDGPELLVRTVEANTGLRIDHYAEIGFGGFAKIVDSVGGVEMNIPKDFKDKWSGADFKKGKQKLSGQEALAFVRTRHAFGSDLERTKNQQKFLSALAHQVATPGTVMNPFKLYPTMGAGLDTLIVDKDMGLFDVASMFWAMKGVTGGDGKSMNMPISGSVGSNLVWDKAKVKQLVEQLNNDETVTVSDN
>NZ_CP030771.1|WP_138960090.1|4071097_4072219_+|membrane-dipeptidase
MADLQDEFDTTAEAGELDRLPDAVPGAGAAEPEPGARLDDADGRARALLAAHPVADGYSGLPWALRGLPYCDLEPGDSCLETDVPRLRAGAVGAQFWSLHVPEDLAGDRAVSATLEQLDLVRHVVTRYGDDLRLARDASEAADARNHGRVATVVGPASARAIGDSLGALRSLHALGLSVLTLAGTSWAGGDGLSAFGEEVVREMNRLGVLADLSGAPEETARRVLSVSRAPVLFTRSGARALCEHPANLGDDLLAAVGAAKGLCLVPFATEQTGTSVRDVVSHLEHVRRIAGPECVGIAGTYDTTAAHPEELDDASRFPRLVTELLGQGWSDAEIGALTWGNVQRALRGADFTARAARERREASTATIGRLDG
>NZ_CP030771.1|WP_138960091.1|4072240_4073566_-|nucleotide-sugar-dehydrogenase
MALKITVIGTGYLGATHAAAMAELGFEVLGLDVVPEKIEMLTRGEVPMYEPGLEELLRRHVAGIEGSSGRLRFTMDFAEAAEFGDVHFVCVNTPQKHGEYACDMSYVDAAFSSLAPHLKPGALVVGKSTVPVGSAQRLSGLLPEGTELAWNPEFLREGFAVDDTLHPDRIVVGVDSERAEKLLRDVYAKPVAEGTPFVVTDFPTAELVKTAANSFLATKISFINAMAEVCEAAGGDVVKLAEALGYDDRIGAKFLRAGIGFGGGCLPKDIRAFMARAGELGADQALTFLREVDSINMRRRGHMVELAREAVGGGSFLGKRVAVLGATFKPDSDDVRDSPALNVAGQIHLQGGQVTVYDPKGMDNARRLFPTLGYAASAEEAVRGADVVLHLTEWREFRDLDPEALGAVAGHRVLLDGRNALDPERWRAGGWTYRAMGRPVA
>NZ_CP030771.1|WP_138960092.1|4073786_4074944_+|acyl-CoA-dehydrogenase-family-protein
MAGSADFDLYRPSDEHVMLRDTIRSLAESKIAPFAAAVDEEARFPQEALDALVASDLHAVHVPESYGGGGADALATVIVIEEVARVCASSSLIPAVNKLGSLPVILSGSEELKKKYMTPLAKGEGMFSYCLSEPDAGSDAAGMKTKAVRDGDSYVLNGVKRWITNAGVSEYYTVMAVTDPEKRSKGISAFVVEKGDEGVSFGAPEKKLGIKGSPTREVYLDNVRIPADRMIGEEGTGFATAMKTLDHTRITIAAQALGIAQGALDYAKGYVQERKQFGKPIADFQGIQFMLADMAMKISAARALTYQAAAASERGDADLTYLGAAAKCFASDIAMEVTTDAVQLLGGYGYTRDYPVERMMRDAKITQIYEGTNQVQRIVMARNLP
>NZ_CP030771.1|WP_138960093.1|4075042_4076026_-|alpha/beta-fold-hydrolase
MGYRPRRGYELISLKLSEETPMSDAVPAVPTDEELAHSLEGDFTSAYAEVNGVRLHYVAGGSGDPLVLLGGWPQTWWQFHKVMPALARRYRVIAVDLRGMGGSAKPPSGYDKKTMAEDIHALVRHLGHDRVHLAGHDIGAMVAHAFAVNHPEATRKLALLDVAHPDPSLRELTLLPVGDGAEWETTPGGVYLWWFAFNQVKGLPERLLAGRTDVLVDWLFGYLLQDQSTIDERSRAVYAAAYATPDAVRAGNAWYQTFLQDVEDFETYDRVGVPVLALAGDRSHAYLRAILPGHAEDFRLRRIEGSGHYLPEERPEQVTAELVEFFA
>NZ_CP030771.1|WP_138960094.1|4076106_4077303_-|membrane-dipeptidase
MTTLTDSLARARSLLAEFPVVDGHNDLPWALREKAGYDLDRLDVGADQSGRLHTDLARLRAGGVGAQYWSVYVRSDMAGDDAVSATLEQIDCVQRLLARHPEELRPALTAADLEAARAEGRIASLMGAEGGHSINNSLATLRALYALGVRYMTLTHNDNIAWADSATDVPGVGGLSAFGREVVREMNRLGMLVDLSHVAATTMRAALDTSEAPVIFSHSSSRAVCDHPRNIPDDVLERLPANGGVAMATFVPKFVLQAAVDWTLAADENMRAHGFHHLDTTPEAMKVHAAFEESHPRPVATAATVADHLDHMREVAGVDHIGIGGDYDGTAFTPSGLDDVSGYPNLVAELLDRGWSEPDLAKLTWRNAARVLGAAEDVARAAKARRGPSIATLEQLDG
>NZ_CP030771.1|WP_138960095.1|4077342_4077882_-|5-(carboxyamino)imidazole-ribonucleotide-mutase
MSTSVSSPVVGIVMGSDSDWPVMEAAAKALDEFEIPYEVDVVSAHRMPREMIAYGEEAAGRGLKVIIAGAGGAAHLPGMLASVTPLPVIGVPVPLKYLDGMDSLLSIVQMPAGVPVATVSVGGARNAGLLAARTLAAHDAELLGRMREFQQELNEQATEKGKRLRAKVEGAGSGFGFGK
>NZ_CP030771.1|WP_138960096.1|4077878_4079030_-|5-(carboxyamino)imidazole-ribonucleotide-synthase
MTFPVVGMVGGGQLARMTHEAGIPLGIRFKLLSDTPQDSAAQVVSDVVIGDYRDLDTLRDFARGCDVITFDHEHVPTEHLRALEADGIPVRPGPDALVHAQDKGVMRAKLDELGVPCPRHRIVEDPADVVAFAAEGATEGDGFPVILKTVRGGYDGKGVWVVRSAADAAEPFRAGVPVLAEEMVDFARELAANVVRSPHGQAVAYPVVESRQVDGVCDTVIAPAPDLSDELAGRAQELALRVAQELGVVGHLAVELFETRDGRVLVNELAMRPHNSGHWSQDGAVTSQFANHVRAVLDLPLGDPRPRAKWTVMTNVLGGDYPDMYTAYLHCMARDPQLKIHMYGKDVKPGRKVGHVNTYGDDLDEVLDRARHAAGYLRGTITE
>NZ_CP030771.1|WP_138960097.1|4079288_4079819_+|GtrA-family-protein
MTDRGALRVRMDRLTREVAKFGAVGAVGTLVNFAVFNLVRHLTDLQVVRASVIATVVAICCNYVGFRYFTYRDRDKNGRTKELTLFLLFSVVGLVIENGVLYVATYGFEWDSKLQANVFKFLGMGIATLFRFWSYRTWVFRALPARAAVADAESFLEDAPAADGGRPAASGGRRQA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_6

4387401-4387554

Orphan

Consensus_repeat	Method
CTCCGGACAGGAGCTGACGGTAGAGCCCACACCAGTGCGGCTTGGTCGGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_6

>merge|NZ_CP030771|6|4387401-4387554|CRISPRCasFinder
CTCCGGACAGGAGCTGACGGTAGAGCCCACACCAGTGCGGCTTGGTCGGAACACTGCCGCCGGACGCACGCCCCGGCCGGGGGCAGATGGCGGGACCACGCCTACTCCGGACAGGAGCTGACGGTAGGGCCCACACCAGTGCGGCTTGGTCGGA

>NZ_CP030771|6|5|4387401-4387554|CRISPRCasFinder
CTCCGGACAGGAGCTGACGGTAGAGCCCACACCAGTGCGGCTTGGTCGGA	ACACTGCCGCCGGACGCACGCCCCGGCCGGGGGCAGATGGCGGGACCACGCCTA
CTCCGGACAGGAGCTGACGGTAGGGCCCACACCAGTGCGGCTTGGTCGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138966668.1\|4396841_4397345_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP030771.1\|WP_138966660.1\|4375301_4378220_+\|winged-helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|276938
NZ_CP030771.1\|WP_138960311.1\|4394874_4396059_+\|acetyl-CoA-acetyltransferase	unknown	unknown	gnl\|CDD\|180434
NZ_CP030771.1\|WP_138960310.1\|4393369_4394704_-\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|132247
NZ_CP030771.1\|WP_138960307.1\|4391056_4391827_-\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319911
NZ_CP030771.1\|WP_138960305.1\|4384683_4385961_+\|phosphopyruvate-hydratase	unknown	unknown	gnl\|CDD\|234617
NZ_CP030771.1\|WP_138966666.1\|4382626_4383058_+\|OB-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|224462
NZ_CP030771.1\|WP_138960306.1\|4388406_4390875_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|270916
NZ_CP030771.1\|WP_138960301.1\|4378803_4379007_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138966662.1\|4379576_4381187_-\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|236072
NZ_CP030771.1\|WP_138966664.1\|4381404_4382544_+\|lipid-transfer-protein	unknown	unknown	gnl\|CDD\|181147
NZ_CP030771.1\|WP_138960303.1\|4383102_4383906_+\|enoyl-CoA-hydratase/isomerase-family-protein	unknown	unknown	gnl\|CDD\|119339
NZ_CP030771.1\|WP_138960313.1\|4397432_4397882_-\|OB-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|224462
NZ_CP030771.1\|WP_138960312.1\|4396161_4396827_+\|pyridoxal-5'-phosphate-synthase	unknown	unknown	gnl\|CDD\|273138
NZ_CP030771.1\|WP_138960302.1\|4379147_4379534_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|380093
NZ_CP030771.1\|WP_138960314.1\|4398179_4399370_+\|NAD(P)-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224983
NZ_CP030771.1\|WP_138960308.1\|4392113_4392761_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP030771.1\|WP_138960304.1\|4384065_4384488_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP030771.1\|WP_138960300.1\|4378442_4378622_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960309.1\|4392785_4393370_-\|nitroreductase-family-deazaflavin-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|211538

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138966668.1\|4396841_4397345_+\|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.	1.93707e-12
NZ_CP030771.1\|WP_138960306.1\|4388406_4390875_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	1.34589e-73
NZ_CP030771.1\|WP_138960311.1\|4394874_4396059_+\|acetyl-CoA-acetyltransferase	gnl\|CDD\|180434	PRK06158, PRK06158, thiolase; Provisional.	5.82057e-131
NZ_CP030771.1\|WP_138960310.1\|4393369_4394704_-\|acyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|132247	TIGR03203, pimD_small, pimeloyl-CoA dehydrogenase, small subunit. Members of this protein family are the PimD proteins of species such as Rhodopseudomonas palustris, Bradyrhizobium japonicum. The pimFABCDE operon encodes proteins for the metabolism of straight chain dicarboxylates of seven to fourteen carbons. Especially relevant is pimeloyl-CoA, basis of the gene symbol, as it is a catabolite of benzoyl-CoA degradation, which occurs in Rhodopseudomonas palustris.	1.61875e-37
NZ_CP030771.1\|WP_138960307.1\|4391056_4391827_-\|VOC-family-protein	gnl\|CDD\|319911	cd07247, SgaA_N_like, N-terminal domain of Streptomyces griseus SgaA and similar domains. SgaA suppresses the growth disturbances caused by high osmolarity and a high concentration of A-factor, a microbial hormone, during the early growth phase in Streptomyces griseus. A-factor (2-isocapryloyl-3R-hydroxymethyl-gamma-butyrolactone) controls morphological differentiation and secondary metabolism in Streptomyces griseus. It is a chemical signaling molecule that at a very low concentration acts as a switch for yellow pigment production, aerial mycelium formation, streptomycin production, and streptomycin resistance. The structure and amino acid sequence of SgaA are closely related to a group of antibiotics resistance proteins, including bleomycin resistance protein, mitomycin resistance protein, and fosfomycin resistance proteins. SgaA might also function as a streptomycin resistance protein.	1.58428e-30
NZ_CP030771.1\|WP_138960305.1\|4384683_4385961_+\|phosphopyruvate-hydratase	gnl\|CDD\|234617	PRK00077, eno, enolase; Provisional.	0
NZ_CP030771.1\|WP_138966666.1\|4382626_4383058_+\|OB-fold-domain-containing-protein	gnl\|CDD\|224462	COG1545, COG1545, Predicted nucleic-acid-binding protein containing a Zn-ribbon [General function prediction only].	9.57418e-15
NZ_CP030771.1\|WP_138966660.1\|4375301_4378220_+\|winged-helix-turn-helix-domain-containing-protein	gnl\|CDD\|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	3.7607e-42
NZ_CP030771.1\|WP_138966662.1\|4379576_4381187_-\|AMP-binding-protein	gnl\|CDD\|236072	PRK07656, PRK07656, long-chain-fatty-acid--CoA ligase; Validated.	0
NZ_CP030771.1\|WP_138966664.1\|4381404_4382544_+\|lipid-transfer-protein	gnl\|CDD\|181147	PRK07855, PRK07855, lipid-transfer protein; Provisional.	0
NZ_CP030771.1\|WP_138960303.1\|4383102_4383906_+\|enoyl-CoA-hydratase/isomerase-family-protein	gnl\|CDD\|119339	cd06558, crotonase-like, Crotonase/Enoyl-Coenzyme A (CoA) hydratase superfamily. This superfamily contains a diverse set of enzymes including enoyl-CoA hydratase, napthoate synthase, methylmalonyl-CoA decarboxylase, 3-hydoxybutyryl-CoA dehydratase, and dienoyl-CoA isomerase. Many of these play important roles in fatty acid metabolism. In addition to a conserved structural core and the formation of trimers (or dimers of trimers), a common feature in this superfamily is the stabilization of an enolate anion intermediate derived from an acyl-CoA substrate. This is accomplished by two conserved backbone NH groups in active sites that form an oxyanion hole.	9.87051e-40
NZ_CP030771.1\|WP_138960312.1\|4396161_4396827_+\|pyridoxal-5'-phosphate-synthase	gnl\|CDD\|273138	TIGR00558, Pyridoxine/pyridoxamine_5'-phosphate_oxidase, pyridoxamine-phosphate oxidase. This model is similar to Pyridox_oxidase from Pfam but is designed to find only true pyridoxamine-phosphate oxidase and to ignore the related protein PhzG involved in phenazine biosynthesis. This protein from E. coli was characterized as a homodimer with two FMN per dimer. [Biosynthesis of cofactors, prosthetic groups, and carriers, Pyridoxine].	2.05367e-48
NZ_CP030771.1\|WP_138960302.1\|4379147_4379534_+\|VOC-family-protein	gnl\|CDD\|380093	pfam18029, Glyoxalase_6, Glyoxalase-like domain. This entry comprises a diverse set of domains related to the Glyoxalase domain. The exact specificity of these proteins is uncertain.	5.06428e-28
NZ_CP030771.1\|WP_138960314.1\|4398179_4399370_+\|NAD(P)-binding-domain-containing-protein	gnl\|CDD\|224983	COG2072, TrkA, Predicted flavoprotein involved in K+ transport [Inorganic ion transport and metabolism].	5.20243e-43
NZ_CP030771.1\|WP_138960308.1\|4392113_4392761_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.2206e-10
NZ_CP030771.1\|WP_138960304.1\|4384065_4384488_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	7.05641e-13
NZ_CP030771.1\|WP_138960313.1\|4397432_4397882_-\|OB-fold-domain-containing-protein	gnl\|CDD\|224462	COG1545, COG1545, Predicted nucleic-acid-binding protein containing a Zn-ribbon [General function prediction only].	1.6859e-21
NZ_CP030771.1\|WP_138960309.1\|4392785_4393370_-\|nitroreductase-family-deazaflavin-dependent-oxidoreductase	gnl\|CDD\|211538	TIGR00026, Hypothetical_protein_Rv1261c/MT1299/Mb1292c., deazaflavin-dependent oxidoreductase, nitroreductase family. This model represents a family of proteins found in paralogous families in the genera Mycobacterium and Streptomyces. Seven members are in Mycobacterium tuberculosis. Member protein Rv3547 has been characterized as a deazaflavin-dependent nitroreductase. [Unknown function, Enzymes of unknown specificity].	1.72514e-23

>NZ_CP030771.1|WP_138960305.1|4384683_4385961_+|phosphopyruvate-hydratase
MTAITSVTGRRVLDSRGNPTVEVDVELADGSLGRAAVPSGASTGAREAVELRDGEPGRWHGKGVDQAVRHVNTELAAAVLGREAEDQAGLDAVLVATDGTPGKSRLGANAILGVSLATAKAAAAAHRLPLYRYLGGSGARLLPVPMMNIVNGGAHADNPLDFQEFMIAPIGAESFAEAVRMGSEIFHTLRRDLLAAGHSTGVGDEGGFAPALRTAEEALDFVVAAVERTGYRPGADIGLVMDPASSEFFRDGVYDYAGEGVRRTPAEHADYLVELVDSYPVVSIEDPMAEDDLDGWRDLTARVGARCQLTGDDVFCTNETLLREGIATGVANSVLVKVNQIGTLTESLATVDAAHRAGYTVVMSHRSGETEDTTIADLAVATGCGQIKTGSLSRSDRTAKYNQLIRIEESLGPTAQYAATQAFPR
>NZ_CP030771.1|WP_138960304.1|4384065_4384488_-|MarR-family-transcriptional-regulator
MPLPESAAVAAELRTAMGKLTRRVKLEDQMPHGQVAVLGALDRSGAMTTSELAADQRVRPQSMARAVGLLMEQGLITRRAHPTDGRKSLVELSTAGRALLEEERGRRADWLARAIEAELTPEERKLLARGIGLVERLAAH
>NZ_CP030771.1|WP_138960303.1|4383102_4383906_+|enoyl-CoA-hydratase/isomerase-family-protein
MCGAGAAAGLRVERDEETGVAVLTLDRPERHNAIDLPLAAGLAAAWREFRHDDAVRAVVLTGAGDRAFCTGIDRAAEVPQPSSPYSLDDPLLTVGPKANDLWKPVLAAVNGMACGGAFYLLGEAEFALAAEHATFFDPHTTYGMVSAYETVYMAQRMPFGEVARTALMGTAERMSARRAYEVGLVSELCPGDGLLPAALRAAATIASYPTESVQGTVRALWATKEAARAQALAQAPHLIALGNAPRARQAALFAGRARGGGGGHRLR
>NZ_CP030771.1|WP_138966666.1|4382626_4383058_+|OB-fold-domain-containing-protein
MLTPVVDDDGAPFWEYAARGELRVQACAADGCGALRFPPRPCCPHCGSFASDWRRMSGKGRIWSYVVPHPPLLPAYAALAPYHPVVVELAEAPHIRLVGNLVARAGASLDSVAAGRPRVGARVQVVFADQGGVVVPRWVLERP
>NZ_CP030771.1|WP_138966664.1|4381404_4382544_+|lipid-transfer-protein
MKDATAIVGIGQTDFARQLPESEKALACRAILAALADAGIAPAEVDAFASYTMEETDEVEVAKAIGAGDVTFFSKAGYGGGGSCATLAHLAAAITTGQATVGVAWRSRKRGSGPRPWKNTAVQLPTPAQWTRPFGLLRPVDEIAMLTRRYMHEYGASRDHLFNVALACRNRANQNPAAIMYERPLTRDMYMTSRWISEPLCLFDNCLETDGALACVLVSAARARDCRHRPVYVHSVAQGLPAQHHGMVNYWNDDPLSGPAWTAARHLWKHADFGPEDVDVAQIYDAFTPLVPLSLEGYGFCDRGEGGAFTEGGALEIGGRLPLNTAGGGLSEAYVHGFNLITEGVRQLRGAGTAQVPGASTCLVTAGEGVPTSAVLLRN
>NZ_CP030771.1|WP_138966662.1|4379576_4381187_-|AMP-binding-protein
MRGDLEWGSVPGLVRAAVRRFGDREAVVEGRTRVTYEELGERVERAAAACLARGVRAGDRVAVWAPNTLDWIVSALGAVSAGAVLVPINTRFKGTEAAYVLRRSRARLLFVTGTFLGTSYVAALRRAAGDGSGDGPLPGLPHLEEVVVLADDAPADFRTWKDFLAGGDAVPDAEVRARADAVEGTWPSDVVYTSGTTGRPKGAVITHAQTLRCYEIWSDLAGLREGDRYLIVNPFFHTFGYKAGIIACLMRGATMIPQPVFDVDTVLANVVGEGVTVLPGPPTLHQALLDHPARDAHDLSALRLVVTGAAVVPPRLVQRLRAELGISTVLTAYGLSEASGIVTMCRRGDPEEVVATTSGRAIPGTEVRIVSVAGETLPPGSPGEVLVRGHHVMSGYYEDPSETKKVLTGDGWLRTGDVGVLDEDGNLRITDRIKDMFIVGGFNAYPAEIEQLLGVHPDVSDVAVIGVADARLGEVGKAYVVRRPGATLTADDVIAWSRREMANYKVPREVEFVPDLPRNASGKVLKGELRRRGVTG
>NZ_CP030771.1|WP_138960302.1|4379147_4379534_+|VOC-family-protein
MTTLVRHITFDCRDAYGLGTFWAGVLGGSLAEDDAPGDPEVLLRTPGGTDLLFVVVPDAKTGKNRVHFDLQPQERSRDEEVERLLKLGATLVADHRRPDGLGWVTLADIEGNEFCVERSAAERAATDG
>NZ_CP030771.1|WP_138960301.1|4378803_4379007_+|hypothetical-protein
MTRTRKILVTLAVVAAASAGASTTAFADSHSPVAAPLGDGHTPVTPQGDGHFPAPPGDGQMPTPPRS
>NZ_CP030771.1|WP_138960300.1|4378442_4378622_+|hypothetical-protein
MSDSKKKKVLKPMGDGHMPAPPEDGPIVPTGDGHMPVPPKGGATTKGDGHMPAPPAKDA
>NZ_CP030771.1|WP_138966660.1|4375301_4378220_+|winged-helix-turn-helix-domain-containing-protein
MQATARFSVLGPVRAWLGEQQLSTGSPQQRALLAALLLRDGRTATASELIDAIWGEEPPSQALAAIRTYASRLRKVLPPGALVSESGGYAVRAAEGALDLAEAETLSAVAERARAQGDLCQARALVNKALSLWDGEPLANVPGPYADAQRTRLEEWRLQLVEARLDMDLEQGCHAESVSELTALTAAHPLRERLRELLMLALYRSGRQAEALAVYADTRRLLADELGVDPRPGLQELQQRILTADPALAEPSAPAAEPSAGVIRPAQLPATVQDFTGRVSFVKELSDILSTAEGRVMAVSALAGIGGVGKTTLAVHVAHAARPHFPDGQLYVDLQGAGPRVAEPETVLGAFLRALGTADPDIPDTLEERAALFRSVLDGRRVLVLLDNARDAAQVRPLLPGTEGCAALVTSRTRMVDLAGAHLVDLDVMSPDEALQLFTKIVGEERVASEREAALDVVAACGFLPLAIRIAASRLAARRTWTVSTLAAKLADERRRLDELQAGDLAVEATFELGYGQLEPVQARAFRLLGLADGPDISLTAAAAMLDLAPEDAEDLLESLVDTSLLESAAPGRYRYHDLVRLYARACAERDELPPSEREAALSRLLDFYLASAARVYAIERPGDRTVDHLESVDHPVRGFEDDARALDWLHAEAACILACAQQSLGRAGLRRAVDLLLAAKDLAESGASSHRFELVTRAACAAAHEAGDPHAEGRARVTLGQVLNKLGSFEQAAVELQRAADHAETTEDPWTRGNAANELAISVGCMNQHAGSDPLALKTVETHVLRAIEAFRLDGNRHGEASSLCNWSRTLAMMGRTDQSIELARQGVALYDELGISFRVANARYALGIGLNQAGRYAEALVQLTDAQRVFAENRQRLWEGAAHYRIAQVHLAARHPAQAAKHAEQALATGCVGGDWMRANVLTVLGKALDSLGQIDRARACWSKALALHEQTGAPEADEVRVLLRPVAAA
>NZ_CP030771.1|WP_138960306.1|4388406_4390875_-|PQQ-binding-like-beta-propeller-repeat-protein
MVDQLTQHDPRRIGPFEVLGRLGAGGMGLVYLARSASGRRVAIKTVRTELAEDQLFRVRFTREVEAARAVSGFYTAAVVDADPRAAVPWLATAYVPAPSLEEIVNEHGPLPTQAVRWLAAGIAEALESIHGAGLVHRDLKPSNVLVVEDGPRVIDFGIASGVSNTRLTMTNVAVGTPAYMSPEQAKDSRSVTGASDVFSLGSTLVFAATGHAPFHGANPVETVFMLLREGPDLEGLPDELRPLIESCMQMEAALRPTPNDLQAQLAPHLFASESSGDDSGTASAWLPERAVALIEARRGGRPPARAATTGSAGRNSRAGAASAPVSLPPPPRQAPAMPAHAPSQAAPSTPSHAASHAPFHGGAPGGAPGFHGGVPDAGPVRLAGAQVPIGPGPRVAEARAAVVPPPSGLAGSWSRSATPAPAQPRANGTAPAAAAPASAPTGAGAAAGGSWRPWRFRMSNDVWGTPAVAGNLVYVTSFEVHALDVGTGRRSFKTRDVAWSMAVADGRIHASDGPTLYALDGSDGTDLWRLSTDAWVYALQADRGTVVTATRGGGVQGWEAANGEKLWEITGAQTEFETPEAAPVIRDGTVYVWKDARLRAVDARSGIERWSYPIGDAASCGGVPVRVTQAADGFVYVAAGTRVLALDVAAGHVRWHFEAPAAFLSPPAFAPGPAVTGGGVYLADYLGTVYALDATDGRDRWRIATESRSSVEPVLVADGHVHVGSGKGLYTLDAVTGTPKWRFQAGGEVVGSPVVADRRIHFGATDHLLYTLKADDGRLRWKLATGGEITGAPVVRDGVVYACSKDRCVYALDAERGTATAR
>NZ_CP030771.1|WP_138960307.1|4391056_4391827_-|VOC-family-protein
MEFAEGVPCWVDAMLPDVEGGKRFYGELFGWTFDSGAGPEHGRYAQALLDGEPVAALAPKPDGRMPTTWTVYLATPDAATAAARVTAAGGQVITEPVPVGAYGTMGLVADPEGAVFGLWQAGGHPGFGALRKPGAYCWTEVHVRDKSVVDPFYEAVFGYGGHDVELGGEEFRTWSPEGAEAGPDTAVGGRAVMSASVPAAMPAHFLSYFAVADCDATAAAARHLGGRVRTEPYDIPYGRVAVLVDNQGAAFGILQD
>NZ_CP030771.1|WP_138960308.1|4392113_4392761_+|TetR-family-transcriptional-regulator
MTGQVRTVDGRVAGRRGQATRQKLLDCLSEMLSSSPYRDVKVIDVARKAGTSPATFYQYFPDVEGAVLEIAEQMATEGAELTHLLEGRSWVGKAGWQTSQDLVDGFLDFWRKNDAILRVVDLGAAEGDKRFYKIRMKILNSVNNSLADTVKELQSKGKVDKDVSPAALAGSLVAMLAAVASHQRGFQTWGVKQAELKPNLAALVHMGVTGKKPTK
>NZ_CP030771.1|WP_138960309.1|4392785_4393370_-|nitroreductase-family-deazaflavin-dependent-oxidoreductase
MAGPGVRLVRKVSATRAFARLAPRVVPAVDRAVHRLTRGKVLLSARMLPGLVLTARGARSGLVRRTPLACVPGRDGSWLLVGSNFGRAAHPAWTANLLAHPDAEVSWRGRDVPVRARLLTGDERTRAWAAALEFWPPYAAYQERVDREIRVFRLERRETRETREKQEKQEKQERGESEEKGRSPVGRGPGAAPG
>NZ_CP030771.1|WP_138960310.1|4393369_4394704_-|acyl-CoA-dehydrogenase-family-protein
MDAACTVEQNEIRRAVREVLSKRRAAEGLRAAVRTPAGYDAALWEALAGRLGLPGLALPEEYGGVGCGPVELALAGEELGRALAPSPLFATAVLAAPLLLRLGTARQRAAFLPRVASGGLTAALAVPGAELGAALGLTGGNGGDWAGGGRAGGVQATAATGTWHLYGQADQVLDGHSAGLLLVAAHAGGFARSRTLLFLVRGDAPGLVRTRRTTLDETRAQARVELRDVRAELLGDGEGADVLPALADVGERAAAVLAAEAVGAADEALARTLGHVREREQFGRPIGSFQAVKHRLADVYVRVCAARSAAYYAAWAAGAVGPAGPLGGEAAADGQAAVDGEAVASAPVAAGVEPGAGLALACALDALRTAAAEAVQLHGGTGFTWEHDAHLFFKRASGDELLFGPAHRLRAHAAERAGLFAPHSHPGRAPVRVGRGATAEEAAV
>NZ_CP030771.1|WP_138960311.1|4394874_4396059_+|acetyl-CoA-acetyltransferase
MPSPSRTGSRKVAVVGVALADCGRLDDATPYALHAQAARRALADAGLGRDAVDGLASAGLGTLAPVEVAEYLGLRPRWVDSTAVGGATWEVMAAHAADAIAAGHANAVLLVYGSTARADVRAGRRTGNLSFGARGPLQFEAPYGHSLIAKYAMAARRHLHEYGTTLEQLASVAVQARANAATNPEAMFREPITVDDVLGGPVIADPFTKLHCCLRSDGGCAVLLAAEDLVRDCAPRPVWVLGTGEHVSHTTMSEWRDFTVSPAAVSGRLAFERAGVRPADIDVAQIYDAFTYMTLVTLEDLGFCAKGEGGAFVEKGRLLRDGELPTNTDGGGLSAQHPGMRGLFLLVEAVRQLRGDAGPGRQVRRADGRLPELAVASGTGGWFCSSGTVVLARG
>NZ_CP030771.1|WP_138960312.1|4396161_4396827_+|pyridoxal-5'-phosphate-synthase
MTTNRFRDLLRSQKVWDTDLPTFDPAATPDAPLGLFHHWFAEAVAAGQTEPHTMTLATTDGAGRADARTVMLHDADAAGWHFASHDISRKGRQLAERPHAALHFYWPAQARQIRLRGPVAVAPHAEALADLHARTTGALAAALVGHQSEVLGSRAELTRASEDAWERAAERPDADAPSWTLYVLAPDEVEFFQGDARRRHVRLRYRAADQQGAWLRELLWP
>NZ_CP030771.1|WP_138966668.1|4396841_4397345_+|GNAT-family-N-acetyltransferase
MTGEDAGLVLRPARAEDAAAVARIWHAGWSDGHLGHVPEALLTVRTPQSFVLRAPRRVDDTVVALVAGVVAGFVMVVDDEVEQVYVSAAHRGTGVAVALLAEAERVVAAKGHRRAWLAVVDGNARARRFYERQGWRDEGLFEYLAASATGPIRVPCHRYVKHLTAPA
>NZ_CP030771.1|WP_138960313.1|4397432_4397882_-|OB-fold-domain-containing-protein
MTADGRPRFDLPEVDAFTRTYWDAAAEGRLLLRRCHAPGCGLAHHYPREFCPHCWSEDVTWERARGDATLYTWSVVHRNDLPPFASRVPYVAAVVDLVEGPRMMTELVGGAEGGLRIGMPLRVAFREAAEGLAVPVFEPGEAPRREHAA
>NZ_CP030771.1|WP_138960314.1|4398179_4399370_+|NAD(P)-binding-domain-containing-protein
MADSNPPPPSTDRPLADRPGPARPVYVIGGGPGGLAVAAALRARGVRAVVLEKSDRVGASWRGHYDRLHLHTTRRLSGLPGLAMPRSFGRWVARDDVVRYLEKYAEYHELDVVTGVEVTRLERADGGGWLLRATGGRELTGRAVIVATGYNHTPHVPDWPGADTFPGDLRHACAYREPSPYADQDVLVVGIGNTGAEIAVDLAEGGAARVRIAVRTAPHIMRRSTAGWPAQRSGILCRRLPVPVVDRLGRAIARVSVPDLSAHGLPRPGTGLYSRVREGAIPVQDVGLIDAVRSGRVEPVAAVESFEGGKVLLADGSRVGPDAVIAATGYRRALEPLLGHLGVLDPRGRPRALGPRTAPEAPDLYFTGFTTPISGTLRELARDAGRIARAVARAGA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_7

4479891-4480033

Orphan

Consensus_repeat	Method
GGGAGGAACCCGCCGCGGTAGCGGCGGGCAACCGGACGACGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_7

>merge|NZ_CP030771|7|4479891-4480033|CRISPRCasFinder
GGGAGGAACCCGCCGCGGTAGCGGCGGGCAACCGGACGACGGCCCGCGAGCCGCGAGGTCGGGGCCGGGCCGGGTCACCCGGGTGACACGGGTGGGCGGGTGGGAGAAACCCGCCGCGGTAGCGGCGGGCAACCGGACGACGG

>NZ_CP030771|7|6|4479891-4480033|CRISPRCasFinder
GGGAGGAACCCGCCGCGGTAGCGGCGGGCAACCGGACGACGG	CCCGCGAGCCGCGAGGTCGGGGCCGGGCCGGGTCACCCGGGTGACACGGGTGGGCGGGT
GGGAGAAACCCGCCGCGGTAGCGGCGGGCAACCGGACGACGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138960373.1\|4473541_4476730_-\|molecular-chaperone-Hsp90	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960372.1\|4472572_4473400_-\|calcium-binding-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960380.1\|4483980_4484979_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl\|CDD\|223682
NZ_CP030771.1\|WP_138966678.1\|4478496_4479873_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340863
NZ_CP030771.1\|WP_138960378.1\|4482948_4483212_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_030363393.1\|4482354_4482738_-\|cold-shock-protein	unknown	unknown	gnl\|CDD\|224197
NZ_CP030771.1\|WP_138960381.1\|4484975_4486055_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl\|CDD\|227119
NZ_CP030771.1\|WP_138960383.1\|4486899_4487871_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|238566
NZ_CP030771.1\|WP_138960369.1\|4468986_4469262_+\|DUF2530-domain-containing-protein	unknown	unknown	gnl\|CDD\|378488
NZ_CP030771.1\|WP_138960371.1\|4471750_4472530_-\|calcium-binding-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960379.1\|4483175_4483841_-\|haloacid-dehalogenase-like-hydrolase	unknown	unknown	gnl\|CDD\|223620
NZ_CP030771.1\|WP_138960375.1\|4480199_4480703_+\|DUF2771-domain-containing-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960374.1\|4476854_4477835_-\|DUF3027-domain-containing-protein	unknown	unknown	gnl\|CDD\|378605
NZ_CP030771.1\|WP_138960368.1\|4467334_4468783_-\|NCS2-family-permease	unknown	unknown	gnl\|CDD\|225161
NZ_CP030771.1\|WP_138960376.1\|4480666_4481407_+\|futalosine-hydrolase	unknown	unknown	gnl\|CDD\|236194
NZ_CP030771.1\|WP_138960370.1\|4469343_4471746_+\|HAD-IC-family-P-type-ATPase	unknown	unknown	gnl\|CDD\|319795
NZ_CP030771.1\|WP_138960366.1\|4466487_4466925_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP030771.1\|WP_138960367.1\|4467092_4467269_+\|ribbon-helix-helix-protein,-CopG-family	unknown	unknown	gnl\|CDD\|372110
NZ_CP030771.1\|WP_138960382.1\|4486051_4486903_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224045
NZ_CP030771.1\|WP_138960377.1\|4481399_4482257_+\|1,4-dihydroxy-6-naphthoate-synthase	unknown	unknown	gnl\|CDD\|270353

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138960367.1\|4467092_4467269_+\|ribbon-helix-helix-protein,-CopG-family	gnl\|CDD\|372110	pfam12441, CopG_antitoxin, CopG antitoxin of type II toxin-antitoxin system. CopG antitoxin is a member of a type II toxin-antitoxin system family found in bacteria and archaea. Most antitoxins encoded by the relBE and parDE loci belong to the MetJ/Arc/CopG family of dimeric proteins which bind DNA through N-terminal ribbon-helix-helix (RHH) motifs. The toxin for CopG proteins falls into the family BrnT_toxin, pfam04365.	0.00627158
NZ_CP030771.1\|WP_138960380.1\|4483980_4484979_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl\|CDD\|223682	COG0609, FepD, ABC-type Fe3+-siderophore transport system, permease component [Inorganic ion transport and metabolism].	7.20282e-81
NZ_CP030771.1\|WP_138966678.1\|4478496_4479873_+\|MFS-transporter	gnl\|CDD\|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.38743e-23
NZ_CP030771.1\|WP_030363393.1\|4482354_4482738_-\|cold-shock-protein	gnl\|CDD\|224197	COG1278, CspC, Cold shock proteins [Transcription].	5.29053e-27
NZ_CP030771.1\|WP_138960381.1\|4484975_4486055_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl\|CDD\|227119	COG4779, FepG, ABC-type enterobactin transport system, permease component [Inorganic ion transport and metabolism].	8.65822e-78
NZ_CP030771.1\|WP_138960369.1\|4468986_4469262_+\|DUF2530-domain-containing-protein	gnl\|CDD\|378488	pfam10745, DUF2530, Protein of unknown function (DUF2530). This family of proteins with unknown function appears to be restricted to mycobacteria.	0.00110897
NZ_CP030771.1\|WP_138960379.1\|4483175_4483841_-\|haloacid-dehalogenase-like-hydrolase	gnl\|CDD\|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	3.5352e-21
NZ_CP030771.1\|WP_138960374.1\|4476854_4477835_-\|DUF3027-domain-containing-protein	gnl\|CDD\|378605	pfam11228, DUF3027, Protein of unknown function (DUF3027). This family of proteins with unknown function appears to be restricted to Actinobacteria.	3.31501e-101
NZ_CP030771.1\|WP_138960368.1\|4467334_4468783_-\|NCS2-family-permease	gnl\|CDD\|225161	COG2252, COG2252, Xanthine/uracil/vitamin C permease [Nucleotide transport and metabolism].	5.00529e-109
NZ_CP030771.1\|WP_138960376.1\|4480666_4481407_+\|futalosine-hydrolase	gnl\|CDD\|236194	PRK08236, PRK08236, hypothetical protein; Provisional.	5.1919e-76
NZ_CP030771.1\|WP_138960370.1\|4469343_4471746_+\|HAD-IC-family-P-type-ATPase	gnl\|CDD\|319795	cd02609, P-type_ATPase, uncharacterized subfamily of P-type ATPase transporter, similar to uncharacterized Streptococcus pneumoniae exported protein 7, Exp7. This subfamily contains P-type ATPase transporters of unknown function, similar to Streptococcus pneumoniae Exp7. The P-type ATPases, are a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids. They are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle. A general characteristic of P-type ATPases is a bundle of transmembrane helices which make up the transport path, and three domains on the cytoplasmic side of the membrane. Members include pumps that transport various light metal ions, such as H(+), Na(+), K(+), Ca(2+), and Mg(2+), pumps that transport indispensable trace elements, such as Zn(2+) and Cu(2+), pumps that remove toxic heavy metal ions, such as Cd(2+), and pumps such as aminophospholipid translocases which transport phosphatidylserine and phosphatidylethanolamine.	0
NZ_CP030771.1\|WP_138960366.1\|4466487_4466925_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	2.30807e-19
NZ_CP030771.1\|WP_138960377.1\|4481399_4482257_+\|1,4-dihydroxy-6-naphthoate-synthase	gnl\|CDD\|270353	cd13635, PBP2_Ttha1568_Mqnd, A menaquinone biosynthetic enzyme exhibits the type 2 periplasmic-binding protein fold. This group includes Ttha1568 (MqnD) from Thermus thermophilies HB8, an enzyme within an alternative menaquinone biosynthetic pathway that catalyzes the conversion of cyclic de-hypoxanthine futalosine to 1,4-dihydroxy-6-naphthoate. Menaquinone (MK; vitamin K) is an essential lipid-soluble carrier that shuttles electrons between membrane-bound protein complexes in the electron transport chain. Ttha1568 has significant structural homology with the members of type 2 periplasmic-binding fold protein superfamily. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.39901e-142
NZ_CP030771.1\|WP_138960382.1\|4486051_4486903_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224045	COG1120, FepC, ABC-type cobalamin/Fe3+-siderophores transport systems, ATPase components [Inorganic ion transport and metabolism / Coenzyme metabolism].	2.71475e-132
NZ_CP030771.1\|WP_138960383.1\|4486899_4487871_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	1.54795e-76

>NZ_CP030771.1|WP_138966678.1|4478496_4479873_+|MFS-transporter
MHSPRPAGRAARALARALHLPFTGTARGIRKATHAHGAGESGLGKLIELHAVNGAGDVLITISLASTVFFSVPTDEARGRVALYLAITMAPFTLLAPVIGPLLDRLPHGRRAAMAGAMLARALLALILSSAVATGGLELYPAALGVLVASKAYGVVRSAVVPRLLPPAFSLVKANSRVTLSGLLATGLAAPVGAGLQALGARWPLYGACVVFIAGTVLSFTLPRKVDSAKGESKALLAADEEHLRLARARDRGDSTRRSRLGLRTVGPAVTHGLAVNAAQRGLSGFLIFFLAFLLREHPLGGQSAAVSLGIVGVAAGTGNALGTAVGAWLKSRAPEMIIVTVVAVVLGVAVCAALFYSPVGIACLAAVAGFAQALSKLSLDALIQRDVPEAVRTSAFARAETLLQMAWVVGGGIGIALPLNGTLGLSVAAAIVAIGWLPTVRGLLAAARRGGSRRVLA
>NZ_CP030771.1|WP_138960374.1|4476854_4477835_-|DUF3027-domain-containing-protein
MSAATTRSRTQRTPRTPDRLCAEAVGFARAAAEEAAAPGVVGEHVEVVVEGDRVVTHLFECKELGYRGWRWAVTVARASRAKVVTLDETVLLPGPDALLAPEWVPWSERLRPGDMGPGDLLPTDAEDLRLEPGYSGEDAPPPNSVLSQELAERADAEYADAEYADATDGTDTVRDTDATATDAVPARGSLAALAEELGMRRARVLSRYGLHTSADRWDEGYGAKTPMAQAAPASCVSCGFLVPIGGSLGQAFGVCANEFGPADGHVVSLAYGCGGHSEAAVMPKPPRPAPPVLDETRVDELPLRPAPDSGSVPPADPGANEDLGHS
>NZ_CP030771.1|WP_138960373.1|4473541_4476730_-|molecular-chaperone-Hsp90
MSKTVRPATEGTDPFGTARLRRSVLEAWAASPARFREDANAEEDLALGGYRDRLVVELAQNASDAAARAGVPGRLALTLQDGVLAAANTGAPLDAAGVESLATLRASAKREGDALRRTTGRFGVGFAAVLSVSDEPAVVGRTGGVRWSLAEARELAAETARFSPGLGDEVRRRDGHVPLLRLPLAAEGSAPDGYDTVVILPLRDVAAEDLVTRLLAGIDDALLLALPGLEEVSVRTPDGTTRVLRRSTDGADTVVADTRKGTTRWRTVTRAGELDTRLLADRPVEERLRPYWQLTWAVPVGDDGTPGAPRTSPVLHAPTPSDEPLGVPALLIGTFPLDTSRRHAAPGPLTDFLVERAADAYAELLAGWRPVTEAVIGLVPGPLGRSELDGALRQAVLDRLPRTAFLPPAAAPVRGPADGRAPEPADEWAQDAAPEALRPRDAEVVEGAGADTVRVLAEVLPSLLPAGLERRGELRTLGVARVPLTEAVDRLAGLEREPSWWRRLYDTLAGVDPDRLSGLPVPLASGRTTIGPRQVLLPAPGDATAPAALARLGLKVAHADAAHPLLEKLGALPATPRAVLTTPQVRAAVAASLDDDSWYDGLDERAGLAADELADLVLGLVRDADLAPGDEPWLGALALPDEDGEPAPAGELVLPGSAFAEVMREGELAFVDADVAGRWGEQPLAACGVLASFTLVRATDVVLDPDDLEPRDGDFAEPDDAGLLDAVDVWCEDVLDRLPDTAVPPVATEIVAVRDLDLVADDQWPRALALLSRPPLRDALTQPVRVLLPDGTTESVRPYTAWWLRGHPVLDGRRPAGLRAAGGDPLLDGLYDSADAAGFDDEQVLRALGVRTSVGALLAEPGGAAELLDRLADPERTVSPAQLHALYGALADVDPEQVTLPDEVRVVLGGEGGEVMCVDTGDAVVADVPDLLPLTAGLPLLPVAPSRAGDLAELLQAERLSAYVRAEVDPASGVEHEVPESVRVLLGPATPATYREHEELVVDGVDLEWRRTPDGTVHAATVEGVAAGLAWAARQWPRRFEVAALLEDPSRTGELARDRWFD
>NZ_CP030771.1|WP_138960372.1|4472572_4473400_-|calcium-binding-protein
MRIRATVAAVSGALALSALLAPAAQAAGPDVTALPKNAQKGDTKITKAVVNGGKDIVVGTTAKKKFTIAVTATDAKGIAGGGGLLWHGRKFDDQNLSGVLAPVADEKCKKLSATSATCTVSITVNPKASWDENGLANHMAGGGWKLFAAAGGTDDDYVIRTAYKTGIHLKRAARLTVNASPEPVRKGETITVAGALTRANWDTRKYAGYTQQPVRLQFKKKGASGYSTLKTVKSDAKGNLRTTVKASADGTFRYVFAGTSTTPAVTSAGDAVDVR
>NZ_CP030771.1|WP_138960371.1|4471750_4472530_-|calcium-binding-protein
MRIRTTVAAVSGAVVLSGLALPAAQAADTHKGHTKITKVVVNGGKDIVLGTSDKKITMTVTGTDPKGIKDGFVALWYGKKLDWSRLDGMLSPAKDPRCTKIDAKRATCKIVTVAHPSGLKNSTAGTWNVVAGLLGKGRAENHVIKEKYKTARVLRAAKLTADASPEPTGKGETITVSGALTRANWESRTYAGYTGQPVKLQFKAAGASAYTTVKTVKSGAKGQLKATVKASVDGTFRYVFGGSASSPAVVSAGDFVDVR
>NZ_CP030771.1|WP_138960370.1|4469343_4471746_+|HAD-IC-family-P-type-ATPase
MTHIDAGAELDPVHPVPPPTGRATGLSAAEVAERVARGEVNDVPVRSSRSTAEIVRANVFTRFNAIIGVLWAIMLFVAPIQDSLFGFVIVANTGIGIIQELRAKKTLDGLAVIGEAKPTVRRDGVAAEISTSEIVLGDLVELGPGDKIVVDGETVESDSLEVDESLLTGEADPVLKKPGDKLMSGSFVVAGGGAFTATKVGREAYAAQLAEEASRFTLVHSELRSGISTILKYVTWLMIPTSIGLVISQLVVKDDNFKESIAYTVGGIVPMIPEGLVLLTSVAFAIGVIRLGRQQCLVQELPAIEGLARVDTVCLDKTGTLTEGGMDVTELRPLNGSDETYVRKVLGALGESDPRPNASLQAIIDAYPDSEEWRCTESLPFSSARKYSGASFSESDGESSTWLLGAPDVLLPAGDPALDEVEDLNHQGLRVLLLARAAGDLDAPDLAAGARPTALVVLEQRLRPDAADTLRYFAEQDVQAKVISGDNAVSVGAVAAKLGLPGAENTVDARQLPKEEAAMAQELDANSVFGRVTPQQKRDMVGALQSKGHTVAMTGDGVNDVLALKDADIGVSMGSGSEATRAVAQIVLLNNSFATLPSVVAEGRRVIGNITRVATLFLVKTVYSVVIALLVVCSQVEYLFLPRHLTLLSTLTIGVPAFFLALAPNKERAKPHFVRRVMRYALPGGIIAALSTFATYLLARHHYVGDGAREAETSAATLTLFLVSLWVLAIIARPYTWWRICLVAAMGLGFLLVLTIPYLQDFFALKLVGTTMPWAAVAIAAVASAATEFAFRWVDRRFAA
>NZ_CP030771.1|WP_138960369.1|4468986_4469262_+|DUF2530-domain-containing-protein
MAKWTPKHEAPEPLEGPVVATITGGTAIWFVLFLAQLPFYGWFDDRDATWWVWTCLAGGGLGLIGIWYVRGREAAIKRAEASRTAAVRDAT
>NZ_CP030771.1|WP_138960368.1|4467334_4468783_-|NCS2-family-permease
MSPSATAPVDAKQPPPNPPQGGLDGFFKISERGSTLAREVRGGFATFFAMAYIIVLNPIILGSAKDMYGHQLDNKQLVTATVLTAAFTTLLMGVIGNVPIALAAGLGVNTVVALQLAPRMSWPDAMGMVVLAGFVVMLLVATGLRERVMSAVPLGLRKGIAIGIGLFIMLIGLVDAGFVSRIPDAAHTTVPLQLGGDGHLNGWPVLVFVLGVLLTLALLVRKVPGAILLSIVVMTAVAMIVHAVADVPSWGLTTPEWPGNPVATPDFGLVGEISLFGGFEKVGVLTGVLFVFTVLLSCFFDAMGTIMGIGDEAHLTDDKGDFPGINKVLFVDGIAVAAGGASSSSATTCFVESTAGVGEGARTGFANVVTGGLFTVALFLTPLATMVPSQAATPALLAVGFLILSGSIGQIDWSDYTIAIPAFVTMLMMPFTYSITNGIGMGFITFTVLRLAAGRGREVPVAMYVVSAVFAFYYLMPALDLT
>NZ_CP030771.1|WP_138960367.1|4467092_4467269_+|ribbon-helix-helix-protein,-CopG-family
MASTVLSLRIDSELLDRLRKHAAKRGMSVQDYVVRTLIRDDFDERFKSSVEETERFYA
>NZ_CP030771.1|WP_138960366.1|4466487_4466925_-|MarR-family-transcriptional-regulator
MPDLSHGDDAAAVNSLRSAVMRLSRRLKHQRVDESLSPTEMSVLGTLARCGNATPGELARKEHVQPPSMTRIVALLEAKGLVRLEPHPDDRRQKVVTQTEQAETMLEESRRKRNAWLARLTEELDDDEWAKLRDAAPVLEKLAHL
>NZ_CP030771.1|WP_138960375.1|4480199_4480703_+|DUF2771-domain-containing-protein
MTSLVPRSARSRRAVASLGAVSAGLLVLSACDKPTPLATVTVGSKSVHSEASCYKDGKELTPSAVQDCLKDTKDIKSITVDPDEKVRFGVDPEIADKGWTLLMNGQPLTEASKKTYVVIPGSVFFNQQYGGGGSSTTVSLLEGGKSEGGAPKATGLWSFKLKKDKDA
>NZ_CP030771.1|WP_138960376.1|4480666_4481407_+|futalosine-hydrolase
MVVQAEEGQGRLTLTGTGRGPRVLVATAVPAERDAVASGLSAGAGPASGAGRVDVLAVGVGPAAAAAGTAAALATAAAHGTPYGLVVSAGIGGGFPPDAPVGSLVVADAVTAADLGAETADGFLPVTELGFGRVTYEPPGTLVRELAAAAGAATGTVLTVSTVTGSAERAAGLRARHPRALAEAMEGFGVAEAAAVHGLPVCEVRAVSNPVGPRDRAAWRIGDALTALTGAFGKFAPVLESWNRHD
>NZ_CP030771.1|WP_138960377.1|4481399_4482257_+|1,4-dihydroxy-6-naphthoate-synthase
MTDTAPGPLRIAYSPCPNDTFVFDAWAHGRVPDAPALDVTFADIDITNGMAERGEFDVLKVSYAVLPYVLDEYALLPCGGALGRGCGPLVLTREPGLDLSGKKVAVPSERSTAYLLFRLWAADVLADGVGEIVVLPFDRIMPAVRDGEVDAGLVIHEARFTYQNYGLHRLADMGEHWEATTGLPIPLGAIIAKRSLGEDALRGLADAARASVRAAWDDPEVSRPYVLEHAQEMDPKVADQHIGLYVNEFTADLGEDGYAAVRGLLTRAAAEGLVPALAPGALAFP
>NZ_CP030771.1|WP_030363393.1|4482354_4482738_-|cold-shock-protein
MPTGKVKWFNSEKGFGFLSRDDGGDVFVHSSVLPDGVDTLKPGQRVEFGVVAGQRGDQALSVTLLDPTPSVAAAQRRKPDELASIVQDLTTLLENITPMLEKGRYPDKASGAKIAGLLRAVADQLDV
>NZ_CP030771.1|WP_138960378.1|4482948_4483212_+|hypothetical-protein
MRDKTQANSTGPGDGLVRIGAIVFFVGAVATLVTVAPLFLGGDPFPPVAYAVCMLMGVGFLIAGAGVFRSIAVQRRQARSAAGPSAT
>NZ_CP030771.1|WP_138960379.1|4483175_4483841_-|haloacid-dehalogenase-like-hydrolase
MTSRTARTTRDGGALTVGFDLDMTLIDSRPGIHACYVALSERTGVYVDADLAVTRLGPPLEQELAHWFPATEVAATAELYREMYPTYAIAATPALPGARAAVDAVRAAGGRAIVVTAKYEPNAKLHIEHLGIAADAVVGNLWAERKAQALHEYGASVYVGDHTGDVRGARTAGALSVAVATGPCDAEELRAAGADVVLGDLSQFPAWLAAHVADGPAADLA
>NZ_CP030771.1|WP_138960380.1|4483980_4484979_+|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MRVNARRAVAMTAAVVALLLAVLFSLAVGARAIAPSAVLDALLHGGHGDAAEVVREMRVPRTVLGVMVGAALAVAGTALQGITRNPIADPGILGISQGASVGVVVAIAYAGTHTLTGYVWYAFTGAALAAVAVYAIAASGRGGATPVKLALGGAAINALLVSVTTGVLTTRASALDEFRFWQVGALSGREAAIVGQTWPFLLAGLLLVLSVARGLDALALGEDVAKGLGQNVALVRVVGGLGATVLTGVGVAAAGPIAFIGLAVPHIARAVIGGDHRWVLPLAALLGPVMLLVSDTVGRIVFPPSEVPAGVMTALIGVPFLVTLVRRKAVAA
>NZ_CP030771.1|WP_138960381.1|4484975_4486055_+|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MSPDVLAAPRRVRPAGYAVVRLGRATFLAHRRATVVATVLALLLAAACLAYLCVGETYVQPVEALKVVLGRPSADELVVGTLREPRMTVGLLVGAAFGVAGALIQTVARNPLASPDIIGISQGASAVTVAAMTFGLTSYTVLPYLSVAGGVAAALLVYAFAWRGGLHATRFVLIGIGFAIALRSVTTLFMTKGDYLVAQQAQIWMTGSLNGRGWPEAGPLALTLLVLLPCVAWAARAQRTVSMDDDTATALGVRLGRVRTGLVLLGVVLASVATGAAGPVDFVALLAPQIARRLTRTAQIPLVSSALLGAIVVVLADLLARRLFSPTELPVGVLTAAVGAPYLIWLIVRSRSVRNGGTA
>NZ_CP030771.1|WP_138960382.1|4486051_4486903_+|ATP-binding-cassette-domain-containing-protein
MSAPAGARLTARELTLAYEDRTVVHALDLAIPDGAVTVVVGPNACGKSTTLRALGRLLKPRGGAVLLDGEELAKLPTRRIAQRIGLLPQTPVAPEAITVADLVARGRQPHQRWWQQWSDADERAVTEAMERTDVTALAERAVDELSGGQRQRVWIAMALAQETELLLLDEPTTYLDIAHQVEVLDLVRQLNHDRGRTVAVVLHDLNQAARYADHLVAMKEGRVVAEGAPRDVVTAELVRDVFGLACVVVPDPVTGSPLVVPGTPWRPPAPEGEKPSPDERSSS
>NZ_CP030771.1|WP_138960383.1|4486899_4487871_+|ABC-transporter-substrate-binding-protein
MNRSSRRRVRTVGALAVTGALALAGCGSSDDDKDAGSGRTHVVKTAMGEVKVPVAPERVVVLDTAELDSALTLGVKPVGATHTDASSGFPGYLPEDELTGIKDVGEMMNPNLEVIAGLKPDLILTSKIRHGAKYDQLKQIAPTVMTETTGYPWKANFRTHADALGKKAAAEKTVAAYDAHVKEVTAAIGGPAKARATEVNVVRFVQGADIRIYGEQSYIATILKDVGLGRAPVSQKAKDGFSYDVSPEKIDLADTDVIFQSTYGDPKKAKQTQTVNSGLWKNMKAVRSGNVHVVDDELWLQGIGYTAADEVLDQLRTALAKRK

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_8

4639280-4639408

Orphan

Consensus_repeat	Method
CCCAGGCGCCCGCGCCCGCGTACGGATCGGCCGCTCAGGGCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_8

>merge|NZ_CP030771|8|4639280-4639408|CRISPRCasFinder
CCCAGGCGCCCGCGCCCGCGTACGGATCGGCCGCTCAGGGCAGCCCCACGCCCGAAGGCGGACCGCCGCCCGACGGGAGACCCGCGCCCCAGGCGCCCGCGCCCGCGTACGGACCGGCCGCTCAGGGCA

>NZ_CP030771|8|7|4639280-4639408|CRISPRCasFinder
CCCAGGCGCCCGCGCCCGCGTACGGATCGGCCGCTCAGGGCA	GCCCCACGCCCGAAGGCGGACCGCCGCCCGACGGGAGACCCGCGC
CCCAGGCGCCCGCGCCCGCGTACGGACCGGCCGCTCAGGGCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_171075790.1\|4633732_4633891_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960498.1\|4645749_4647177_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|315512
NZ_CP030771.1\|WP_138960493.1\|4635844_4636546_-\|phosphatase-PAP2-family-protein	unknown	unknown	gnl\|CDD\|239480
NZ_CP030771.1\|WP_138960491.1\|4631916_4632285_+\|metal-sensing-transcriptional-repressor	unknown	unknown	gnl\|CDD\|197385
NZ_CP030771.1\|WP_171075791.1\|4636804_4637986_-\|C40-family-peptidase	unknown	unknown	gnl\|CDD\|381602
NZ_CP030771.1\|WP_138960495.1\|4637952_4638333_+\|DUF397-domain-containing-protein	unknown	unknown	gnl\|CDD\|377231
NZ_CP030771.1\|WP_138960500.1\|4649392_4650355_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213235
NZ_CP030771.1\|WP_138966725.1\|4639752_4641228_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_016644813.1\|4631128_4631749_-\|DUF47-domain-containing-protein	unknown	unknown	gnl\|CDD\|224310
NZ_CP030771.1\|WP_138966718.1\|4632409_4632598_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_171075794.1\|4647178_4648699_+\|type-VI-secretion-protein	unknown	unknown	gnl\|CDD\|378923
NZ_CP030771.1\|WP_138960501.1\|4650351_4651134_+\|ABC-transporter-permease	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960492.1\|4632779_4633586_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960496.1\|4642010_4642841_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960499.1\|4648695_4649256_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP030771.1\|WP_030689133.1\|4641509_4641818_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_171075793.1\|4644161_4645721_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960497.1\|4642830_4644165_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|312941
NZ_CP030771.1\|WP_171075792.1\|4638334_4638895_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP030771.1\|WP_138966721.1\|4633984_4635583_+\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223354

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138960498.1\|4645749_4647177_+\|ATP-binding-protein	gnl\|CDD\|315512	pfam12846, AAA_10, AAA-like domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily. Many of the proteins in this family are conjugative transfer proteins.	1.28259e-10
NZ_CP030771.1\|WP_138960493.1\|4635844_4636546_-\|phosphatase-PAP2-family-protein	gnl\|CDD\|239480	cd03385, PAP2_BcrC_like, PAP2_like proteins, BcrC_like subfamily. Several members of this family have been annotated as bacitracin transport permeases, as it was suspected that they form the permease component of an ABC transporter system. It was shown, however, that BcrC from Bacillus subtilis posesses undecaprenyl pyrophosphate (UPP) phospatase activity, and it is hypothesized that it competes with bacitracin for UPP, increasing the cell's resistance to bacitracin.	2.81559e-22
NZ_CP030771.1\|WP_138960491.1\|4631916_4632285_+\|metal-sensing-transcriptional-repressor	gnl\|CDD\|197385	cd10148, CsoR-like_DUF156, Transcriptional regulators CsoR (copper-sensitive operon repressor), RcnR, and FrmR, and related domains; this domain superfamily was previously known as DUF156. This superfamily includes various transcriptional regulators that respond to stressors including Cu(I), Ni(I), sulfite, and formaldehyde. It includes CsoR (copper-sensitive operon repressor) from Mycobacterium tuberculosis (MtCsoR), Bacillus subtilis (BsCsoR), Thermus thermophilus (TthCsoR), and Staphylococcus aureus (SaCsoR), Mycobacterium tuberculosis RicR (regulated in copper repressor, MtRicR), Escherichia coli RncR (formally known as YohL, nickel and cobalt-sensitive), Alcaligenes xylosoxidans NreA (nickel-sensitive), E. coli FrmR (formally known as YaiN, formaldehyde sensitive), and Staphylococcus aureus CstR (CsoR-like sulfur transferase repressor, NWMN_0026.5, SaCstR). CsoR is Cu(I)-inducible, and regulates the expression of genes involved in copper homeostasis. For example, TthCsoR binds the promoter region of the copZ-csoR-copA operon, and represses expression of these genes, which encode the copper chaperone CopZ, CsoR, and the copper efflux P-type ATPase CopA, respectively. In the presence of excess Cu(I), TthCsoR binds this ion, and is released from the DNA, allowing expression of the downstream genes. TthCsoR also senses other metal ions such as Cu(II), Zn(II), Ag(I), Cd(II) and Ni(II). CsoRs form a homotetramer (dimer of dimers). In the case of MtCsoR, two Cys residues on opposite subunits within each dimer, along with a His residue, bind the Cu(I) ion. These residues are conserved in the majority of members of this superfamily. Exceptions include the functionally uncharacterized Bacillus subtilis YrkD where there is an Asn instead of His (C-N-C), E.coli RcnR where there is a Thr instead of the second Cys (C-H-T), or TthCsoR and E.coli FrmR where there is a His instead of the second Cys and which have an additional N-terminal His (not found in those family members having C-H-C) that may also be involved in metal binding (H-C-H-H). A conserved Tyr and a Glu residue facilitate allosteric regulation of DNA binding. SaCstR regulates genes predicted to function in sulfur metabolism; it is thought that oxidation of the intersubunit Cys pair to a mixture of disulphide and trisulphide linkages by sulfite, results in a reduced affinity of SaCstR for the operator DNA. SaCstR exists as a mixture of oligomeric states, including dimers, tetramers and octamers. The sequence of SaCstR was not available at the time this hierarchy was curated and therefore was not included. Escherichia coli RncR represses expression of the gene encoding the nickel and cobalt-efflux protein RcnA. The gene encoding Alcaligenes xylosoxidans NreA is part of the nre nickel resistance locus located on the pTOM9 plasmid from thisbacteria. Escherichia coli FrmR regulates the formaldehyde degradation frmRAB operon.	4.14326e-33
NZ_CP030771.1\|WP_171075791.1\|4636804_4637986_-\|C40-family-peptidase	gnl\|CDD\|381602	cd13399, Slt35-like, Slt35-like lytic transglycosylase. Lytic transglycosylase similar to Escherichia coli lytic transglycosylase Slt35 and Pseudomonas aeruginosa Sltb1. Lytic transglycosylase (LT) catalyzes the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc) as do "goose-type" lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. Proteins similar to this this family include the soluble and insoluble membrane-bound LTs in bacteria, the LTs in bacteriophage lambda, as well as the eukaryotic "goose-type" lysozymes (goose egg-white lysozyme; GEWL).	4.85152e-34
NZ_CP030771.1\|WP_138960495.1\|4637952_4638333_+\|DUF397-domain-containing-protein	gnl\|CDD\|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	0.00200767
NZ_CP030771.1\|WP_138960500.1\|4649392_4650355_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213235	cd03268, ABC_BcrA_bacitracin_resist, ATP-binding cassette domain of the bacitracin-resistance transporter. The BcrA subfamily represents ABC transporters involved in peptide antibiotic resistance. Bacitracin is a dodecapeptide antibiotic produced by B. licheniformis and B. subtilis. The synthesis of bacitracin is non-ribosomally catalyzed by a multi-enzyme complex BcrABC. Bacitracin has potent antibiotic activity against gram-positive bacteria. The inhibition of peptidoglycan biosynthesis is the best characterized bacterial effect of bacitracin. The bacitracin resistance of B. licheniformis is mediated by the ABC transporter Bcr which is composed of two identical BcrA ATP-binding subunits and one each of the integral membrane proteins, BcrB and BcrC. B. subtilis cells carrying bcr genes on high-copy number plasmids develop collateral detergent sensitivity, a similar phenomenon in human cells with overexpressed multi-drug resistance P-glycoprotein.	5.97718e-90
NZ_CP030771.1\|WP_016644813.1\|4631128_4631749_-\|DUF47-domain-containing-protein	gnl\|CDD\|224310	COG1392, COG1392, Phosphate transport regulator (distant homolog of PhoU) [Inorganic ion transport and metabolism].	1.13928e-31
NZ_CP030771.1\|WP_171075794.1\|4647178_4648699_+\|type-VI-secretion-protein	gnl\|CDD\|378923	pfam12696, TraG-D_C, TraM recognition site of TraD and TraG. This family includes both TraG and TraD as well as VirD4 proteins. TraG is essential for DNA transfer in bacterial conjugation. These proteins are thought to mediate interactions between the DNA-processing (Dtr) and the mating pair formation (Mpf) systems. This domain interacts with the relaxosome component TraM via the latter's tetramerisation domain. TraD is a hexameric ring ATPase that forms the cytoplasmic face of the conjugative pore.	7.9531e-06
NZ_CP030771.1\|WP_138960497.1\|4642830_4644165_+\|hypothetical-protein	gnl\|CDD\|312941	pfam09606, Med15, ARC105 or Med15 subunit of Mediator complex non-fungal. The approx. 70 residue Med15 domain of the ARC-Mediator co-activator is a three-helix bundle with marked similarity to the KIX domain. The sterol regulatory element binding protein (SREBP) family of transcription activators use the ARC105 subunit to activate target genes in the regulation of cholesterol and fatty acid homeostasis. In addition, Med15 is a critical transducer of gene activation signals that control early metazoan development.	0.00144742
NZ_CP030771.1\|WP_138960499.1\|4648695_4649256_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.6724e-13
NZ_CP030771.1\|WP_171075792.1\|4638334_4638895_+\|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.	1.05884e-15
NZ_CP030771.1\|WP_138966721.1\|4633984_4635583_+\|FAD-binding-protein	gnl\|CDD\|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	5.81148e-34

>NZ_CP030771.1|WP_171075792.1|4638334_4638895_+|GNAT-family-N-acetyltransferase
MTAHQHGPLPTHQHAPLPARLRPAEPGDHAAIVAAVRTWWTDRSPAEMRELSLLLPKLFLQFFARTSLVREDADGVRAFLVGFHPADHPDEAYIHFVGVDPALRGQGAGRELYEAFFREAAAAGRTRVRSVTSPTNTRSIAFHRALGFRLQDGDGVGPDGVPVHKDYDGPGLDRVCFLRTLTVTDD
>NZ_CP030771.1|WP_138960495.1|4637952_4638333_+|DUF397-domain-containing-protein
MSYAPSTTPRPPGVRRGQCRCGTPAPGGSSSVRRRIIGSARPPRRRPRPVTDARPDLPADLEWIRAAPEGDRGPGPWIEYAFGPDDAVHLRETGAPDRVVTTTRAKWEAFVLGVRAGEFDHFAEGH
>NZ_CP030771.1|WP_171075791.1|4636804_4637986_-|C40-family-peptidase
MGEGWLTVRKTWLLASVAFSGSMGFIGLLVVGTFVAAGSVAGGGGTRGSVGLAKGAVPTTYQPLVQKWGNLCKAINPALLAAQLYQESGFNPSAKSPARAQGIAQFIPGTWATHGIDGDGDGDRDVWDPKDAIPSAASYDCKLAKYVKDAPGDPTRNMLAAYNAGAYAVIKYGGVPPYRETQNYVKIITTLEKSFARPVGRVNPSRQAAGAIYYAQKKLGTLYLWGGNGTADQGGRFDCSGLTLAAYRSVGIPLPRVANDQYNAGPHPKRDELLPGDLVFFSDDLSNSRAIRHVGIYVGGGYMIDAPRPGAKIRFDPVDTPDYFGATRVTEDGAKAVPSESPEEREEKPKKDREPAGEPSSPPSRRPSEEPSEESSTAPSVPSDAPQPEGTDV
>NZ_CP030771.1|WP_138960493.1|4635844_4636546_-|phosphatase-PAP2-family-protein
MAGLDTSGSNPDVSLLYDINGLAKDSPGFVARAMEFIGEYGLLAALVLLVLWCWWGARKRGALDDAAGSVAAVVWAPLAAAIAVLVNVPIRNFVERPRPFRDHQGLEVLVDGKNDYSFVSDHATLAMAIGVGLFVAHRKFGIAGIALAALEGFCRVFMGVHYPTDVIGGFALGTAVTLLLSPLAMALLTPVTKAIGRSGRAARLVWAPHRGARPVATLPEQEAAGSDEKGLAA
>NZ_CP030771.1|WP_138966721.1|4633984_4635583_+|FAD-binding-protein
MARRTFIGTAAAAVAAAGTAACSGGSGGTGGASGSASASGTAGSATASTATTPIRTAAASAAANLTALARDLDGSLVRPNEAHWATARQLYNTRFDSLKPTAVAYVAHPDDIRTALAYARAHDVPVAVRNGGHSYAGWSSGTGRLILDVSRLNRTRVSGSTATIGGGAKLIDVYRALAAKGVTIPAGSCPTVGISGLTLGGGHGVVSRAYGLTCDSLTSATLVTAAGKLIRADKSEHKDLFWALRGAGNGQFGVVTELTFRTHPAPQAVSAYLTWPWAKAAAVVKAWQEWGPAQPDEIWSSLHLAAVPGGTPTVSVAAFSLGTYGGLQNAVDRLADKVGAPARSVSLKRRGYEEAMEVYAGCSSFATDAQCHLPGTTPGRTPTGALGRETYAARSDFFDRSLSAAGIRALLGQMEHVRGERGTAGSIALTALGGAINRVDPTATAFVHRRSRMLAQYIASWRAGTSGTGAQGWLKGAHGAMRRHASGAAYQNYTDATLTNWREAYYGQAAPRLKKVKKAYDPTRFFSFPQAL
>NZ_CP030771.1|WP_171075790.1|4633732_4633891_+|hypothetical-protein
MPESHSPEPTHRTTTVENGRFCAARCSCGWRGPARRARSKARADAAAHSETL
>NZ_CP030771.1|WP_138960492.1|4632779_4633586_-|hypothetical-protein
MGQQHRHTGTAAVAAAVGLMTLATGCSGGGAAASDDPAKEVRDAADALVRAGSSRARTSMEMASGGTRVTVRGQGTYDYRRRQGRFEVVLPQDPADRGRRRPPVTELMTGGDLYMKNRGAGVPADKWVRVDTASLSDGNLVTGGATDPLVAAELLRGARQVTYVRETRVDDVAVRHYRGVAELAGAVPGASAPYRDALRAAVAKGFSKGGVPFDAYLDEQGRLRKLRHRFQVANAEVASTTSLYGFGAPVRVRLPPEKDIYAGKIAER
>NZ_CP030771.1|WP_138966718.1|4632409_4632598_-|hypothetical-protein
MALVRGTAVQDHVALAEIELCGELIIAASAAHGERLSADRIDEVLRVSDAQQDDGPSPARGT
>NZ_CP030771.1|WP_138960491.1|4631916_4632285_+|metal-sensing-transcriptional-repressor
MTTTEAAAAATTTDAPSGSAQTADHAGHQTHGYHKQKDEHLKRLRRIEGQIRGLQRMVEEDVYCIDILTQVSAGTKALQSFALQLLEEHLRHCVADAAVKGGDEIDAKVEEATKAIARMLRT
>NZ_CP030771.1|WP_016644813.1|4631128_4631749_-|DUF47-domain-containing-protein
MRFRLTPRETSFYDMFAASADNIVTGSKLLMELLGADASARAEIAERMRAAEHAGDDATHAIFHQLNSSFITPFDREDIYSLASSLDDIMDFMEEAVDLVVLYQVEELPKGVEQQIEVLARAAELTAEAMPHLRTMDNLTEYWIEVNRLENQADQIHRKLLAHLFNGKYDAIEVLKLKQIVDVLEEAADAFEHVANTVETIAVKES
>NZ_CP030771.1|WP_138966725.1|4639752_4641228_+|hypothetical-protein
MRPVAAALLNLTGLGLGYVLVRAWLPAVLCWAATAGLLLIALPADVDGVPGGLLVGYLALLVLAAADAARRARRTALAWRLRAPLAAALGVVLLAVPAASAFAYEAARDEAVEDMLLERLDEADRLVADQDGQDFAGSERAYRSALDTYRDLVRDHGGSRAADRVPDRLDAYYKAVARPYADGRYCQAIAPLTYLRTLPDRIGENRLGRLATWPDDRLATSLYECGSAAVDRGDGTHLQELLTTFPDSDAARKVVPALGAAIDDRTADLKGPDPCSATEKLTRVRAVAASLPGGKGGSLTARAERAVQSGEYACGVDEFKDGQFTEAAKRMRDYADTYKASGKRERARTIAIAAEVAAERPQAGRKLPAQRGPGSGQEFVVKNDGASAVEVLFTGPATGTVKLGACAGCTPYASRAEGKSKACKASRSYPQKTLRLPPGEYHFLYKRGTGGTGLVRDHSDGTTVQGGYRYTDCTYVVSGGLGGIGGLSPRT
>NZ_CP030771.1|WP_030689133.1|4641509_4641818_+|hypothetical-protein
MLMAAEKGDITTIIGGIAPDWGPFGSLGNEARVMIEVVMAVAILLCLGIAIWGAAKQRIGATALRDTFSAEQGKGLIIAGLTGVFIIGSLGTLFTIVYGMAV
>NZ_CP030771.1|WP_138960496.1|4642010_4642841_+|hypothetical-protein
MSDDDDLFGGTGETRTRLPEREDGYGGARRSGRPGGRSSSRSLVTVIGVVVLLIAAIAFANRDDSSSDGDGGGAHDKGAKTSPTAPTGEKPVTGKNGSIPTGYAKTEQGAQSAAANYAVALGSAEMFDKSKRDGILKAIMAPSSVTKFEAVLDKAYSADFFKNVGLNANGSTPSGYQFVSRTSPIGTKVTDFADGRATVAAWCGGLLGLAGERSTKPVTNSWFTITMKLAWIDGDWKITTHTQKDGPAPVPGDDRASGSEEIADAVEGYGGFTYAR
>NZ_CP030771.1|WP_138960497.1|4642830_4644165_+|hypothetical-protein
MRGSRPVLKLTAALAAIQTAVLLLATRAAAAPDDDPCALIHGPAKKYCEQGEGGGGGGGGRKTPDNGALSELDPLSSLARGFGDAASWIVNKLTEYVNDTAAVDFTNEKFLQQYAVVFAASTILTLIVWLLAVTKRAVRGVPLLTALSEAIGFLWLTVLASAFTPLILSTVVSATDGVSEVLAKSVGGDTDRFFGTFSQALDKGTDIGGGPIMLIVVSAVSIAAAGILCLELVIRAAMLYVGALLGTVVYSGLVDKNTWGRIRRWAGLMVAIILVKPIIVIVLGVAGALQGEDGPDSLSAVVSGLSVILLAIFASASIYRFIPGFGDDIMATRNNRLMRGAENRAATALNSPAAWVAQGIRTHSARPGGKAGGGQGGGGDTPPQTAAANAVGSGLSSHAHRQAGPAQNGGGTVPSAAPPPRTSPSNTPHAGNRGGTNSTGGEGR
>NZ_CP030771.1|WP_171075793.1|4644161_4645721_+|hypothetical-protein
MTTQSHVSPPVTPRRTYLIGRARPNAIIGRNRETGEIALIIAGAFLGMMCGILIPFLALRIVLLMGFPLIAIAAVYIPYKGRTFYKWFEINRSFKRSLRRGTTYRSSAAESGIRLDGREVEIGPPPGIGRISWLAAPFGPDEIAVLLHADRRTVTAAIEIEGPGVGLRDSEDQEALVDRFGTLLKHVANGDGFVTRLQMLARTLPADPDAHAKDVAARGDDRALPWLQHSYDELQSMVSTSSEQHRAYLVACMHYSRDLAAEAQAMARAARPHGGRKLDRDAGLAVVMARELTDICSRLQEADIRVRQPLGQGRLASLVHSMYDPDHPIDHIQAMTKRNAWPAELDAMEPTYLQAKTRESSTRAPWCHSTAWVKEWPMTPVGVNFLAPLLVHTPDVIRTVAVTMDLEPTEVAIERMLTEKTNDEAEASRQAKMNRTVDPRDIASHSRLDQRGEDLASGAAGVNLVGYITVSSRSPEALARDKRTIRASAGKSYLKLEWCDREHHRAFVNTLPFATGIRR
>NZ_CP030771.1|WP_138960498.1|4645749_4647177_+|ATP-binding-protein
MRDPLTVLTDAFTSFLFGKVETTRLPVRTSTGQAQAVYLPTAAPGLGDSGVIIGREVYSGKGYIYDPFQLYGQQLPAPHWLVLGESGNGKSALEKTYVLRQLRFKDRQVVVLDAQGEDGVGEWNLIAQELGITPIRLDPTAALDMGIRLNPLDPAITTTGQLALLRTIIEVAMGHGLDERSGFALKVAHAYVNETILDRQPVLTDIVEQLRHPEPESAEAMNVAIDDVRAWGLDVALVLDRLVDGDLRGMFDGPTTVGIDLDAPLIVFDLSHIDRNSIAMPILMAIVGVWLEHTWIRPDRKKRIFLVEEAWHIINSPFVAQLFQRLLKFGRRLGLSFVAVVHHLSDVVDGAAAKEAAAILKMASTRTVYAQKADEARATGRVIGLPRWAVEIIPTLTPGIAVWDVNGNVQVVKHLITETERPLVFTDRAMTESASDLLATDDVLAAAEREAEERAAYMEQQMGEGPAGSSRSTVA
>NZ_CP030771.1|WP_171075794.1|4647178_4648699_+|type-VI-secretion-protein
MAQDRYRDRRQDQPGRERGVPDALLVGVLAFVVGMVFLMWSATGIAGWWAHGAWPDHVTFNNTPPAVRHLVQEPHDVAGAWPGTPRDQLSGYGLFWGFLIGQVMVLIVLTIFVMGTLTRFRAVRKAARHAETTTSDTAVGNRPAGRDGWAQPPAPSNRDAEPRTGAPEQPLEAEPEPRPAPEPAPAPALAKRPPTVPTPRTPLVLGTPETRRPLAAEAIADAESATLVITSDPTLWEETKDARAKLGPVLVYDPVHLCDTPARLHWSPTTGCEDKATATHRARALLAPIRPTAKLDTAVADTAELLLRSFLHAAAVDGRSVKHVHRWAQGTQVQDAVRVLRTHPKAAPGAAGELESALTAYAERRDMAQELTSRALSCLFTLNVRESCTPNRADSLSLESLVDEGGTLFVVGEAIEDPKANPGAMPLLTALASSMVERGRRLADRSPAGRLDPPLTLVLDDVAAVAPLPQLPELLAAGADQGMPTLALLRSREQGRARWPHDELIG
>NZ_CP030771.1|WP_138960499.1|4648695_4649256_-|GNAT-family-N-acetyltransferase
MEHLIRPVRGDEWRQVRALRLLALRDPAAPVAFLETYEKAVAQPDEYWQDRTTNAAPGGPIRQFVAEGPDGGWAGSVTVLVEEPGTQSVLGAGVEVRQAHLVGVYVRPEHRGTGLTEALFEAAVEWARAADGAGVERIRLFVHEDNERAEAFYRRFGFVRSGLSASVPGDPSALEYEMVLAPAPGR
>NZ_CP030771.1|WP_138960500.1|4649392_4650355_+|ATP-binding-cassette-domain-containing-protein
MIRAQGLTKRYGRGARTKTAVDDLSFEVHPGTVTGFLGPNGAGKSTTMRMLLGLDAPTSGRCTVGGRAYATHSAPLTEVGALLEARSLHPGRSAYHHLTALAHTHGIPRSRVEHVLAATGLTDVAGRRVKGFSLGMGQRLGIAAALLGDPATLVLDEPVNGLDPDGVLWIRNLLKAQAAEGRTVLVSSHLMSEMAVTADHLIIIGRGRLLADTTVEKFVRESGTGSVKVVSPAAARLAALLAGPGVTVDGDTTGPLDAPGALEVRGTDAEHIGRTAAAHAIPLFELTPHTASLEQAFMDLTHDSVEYVTPDVAPLEGAAA
>NZ_CP030771.1|WP_138960501.1|4650351_4651134_+|ABC-transporter-permease
MTTTTPTPSYRVTPARVLRSEWHKLWTLRTTWITVLAASALVLAVGITMGSTYDGDDSDVDTIVFTLFGTQLSQICLAVLGILVTAGEYSTGMIRASLTAVPRRRPVLWSKAAVFTAVAFTLSFVTNVITFLTAQIWLADTDKKLTLTDSGVLGALTGNAAGVTLLSLIALGLGALLRSVPGGIGAFVGSVLVLPEIVGTLPFGGVDAVVRCFPAQAASSLGSLTRVDDTIAPGPALFTLVLWALAVLTAASYLLKRRDV

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_9

5175192-5175307

Orphan

Consensus_repeat	Method
GGGATCCGTGGGGCGCCGCGCGCGGGTGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_9

>merge|NZ_CP030771|9|5175192-5175307|CRISPRCasFinder
GGGATCCGTGGGGCGCCGCGCGCGGGTGCTTGGTGTCTGACCCTGGCCGCGTATGCACGGGGTGGTCCCGCCGCCGCCTCACCCGGGGGATCCGTGGGGCGCCACGCGCGGGTGCT

>NZ_CP030771|9|8|5175192-5175307|CRISPRCasFinder
GGGATCCGTGGGGCGCCGCGCGCGGGTGCT	TGGTGTCTGACCCTGGCCGCGTATGCACGGGGTGGTCCCGCCGCCGCCTCACCCGG
GGGATCCGTGGGGCGCCACGCGCGGGTGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_030688977.1\|5171602_5171968_-\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|377953
NZ_CP030771.1\|WP_138960901.1\|5172075_5172561_-\|winged-helix-DNA-binding-protein	unknown	unknown	gnl\|CDD\|224759
NZ_CP030771.1\|WP_138960902.1\|5172749_5174255_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|129794
NZ_CP030771.1\|WP_171075815.1\|5180593_5181355_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP030771.1\|WP_138960903.1\|5176288_5176954_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960895.1\|5166299_5167928_-\|cytochrome-c-oxidase-subunit-I	unknown	unknown	gnl\|CDD\|238832
NZ_CP030771.1\|WP_138960899.1\|5170656_5171034_+\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915
NZ_CP030771.1\|WP_138960896.1\|5168034_5168571_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP030771.1\|WP_138966837.1\|5165952_5166294_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960900.1\|5171105_5171438_-\|antibiotic-biosynthesis-monooxygenase	unknown	unknown	gnl\|CDD\|224278
NZ_CP030771.1\|WP_138960909.1\|5185966_5187568_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP030771.1\|WP_138960906.1\|5183239_5183929_+\|response-regulator	unknown	unknown	gnl\|CDD\|223816
NZ_CP030771.1\|WP_138960905.1\|5179391_5180597_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223650
NZ_CP030771.1\|WP_138960898.1\|5169419_5170442_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960897.1\|5168563_5169400_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138966841.1\|5181351_5183130_-\|peptidoglycan-binding-protein	unknown	unknown	gnl\|CDD\|367272
NZ_CP030771.1\|WP_138960908.1\|5185451_5185970_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138960907.1\|5183925_5185455_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|182539
NZ_CP030771.1\|WP_138960910.1\|5187564_5189142_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP030771.1\|WP_138960904.1\|5177740_5179213_-\|ornithine-decarboxylase	unknown	unknown	gnl\|CDD\|99739

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_030688977.1\|5171602_5171968_-\|PH-domain-containing-protein	gnl\|CDD\|377953	pfam08000, bPH_1, Bacterial PH domain. This family contains many bacterial hypothetical proteins. The structures of Structure 3hsa and Structure 3dcx show similarities to the PH or pleckstrin homology domain. First evidence of PH-like domains in bacteria suggests role in cell envelope stress response.	2.2303e-62
NZ_CP030771.1\|WP_138960901.1\|5172075_5172561_-\|winged-helix-DNA-binding-protein	gnl\|CDD\|224759	COG1846, MarR, Transcriptional regulators [Transcription].	3.90846e-13
NZ_CP030771.1\|WP_138960902.1\|5172749_5174255_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	8.78233e-65
NZ_CP030771.1\|WP_171075815.1\|5180593_5181355_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	5.15314e-104
NZ_CP030771.1\|WP_138960895.1\|5166299_5167928_-\|cytochrome-c-oxidase-subunit-I	gnl\|CDD\|238832	cd01662, Ubiquinol_Oxidase_I, Ubiquinol oxidase subunit I. Ubiquinol oxidase, the terminal oxidase in the respiratory chains of aerobic bacteria, is a multi-chain transmembrane protein located in the cell membrane. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. The number of subunits in ubiquinol oxidase varies from two to five. Subunit I contains a heme-copper binuclear center (the active site where O2 is reduced to water) formed by a high-spin heme and a copper ion. It also contains a low-spin heme, believed to participate in the transfer of electrons from ubiquinol to the binuclear center. For every reduction of an O2 molecule, eight protons are taken from the inside aqueous compartment and four electrons are taken from ubiquinol on the opposite side of the membrane. The four electrons and four of the protons are used in the reduction of O2; the four remaining protons are pumped across the membrane. This charge separation of four charges contributes to the electrochemical gradient used for ATP synthesis. Two proton channels, the D-pathway and K-pathway, leading to the binuclear center have been identified in subunit I. It is generally believed that the channels contain water molecules that act as 'proton wires' to transfer the protons. A well-defined pathway for the transfer of pumped protons beyond the binuclear center has not been identified. Electrons are believed to be transferred directly from ubiquinol (the electron donor) to the low-spin heme, and directly from the low-spin heme to the binuclear center.	0
NZ_CP030771.1\|WP_138960899.1\|5170656_5171034_+\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	5.14206e-07
NZ_CP030771.1\|WP_138960896.1\|5168034_5168571_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	4.37806e-19
NZ_CP030771.1\|WP_138960900.1\|5171105_5171438_-\|antibiotic-biosynthesis-monooxygenase	gnl\|CDD\|224278	COG1359, COG1359, Uncharacterized conserved protein [Function unknown].	3.3066e-23
NZ_CP030771.1\|WP_138960906.1\|5183239_5183929_+\|response-regulator	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	6.95276e-83
NZ_CP030771.1\|WP_138960905.1\|5179391_5180597_-\|ABC-transporter-permease	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	3.17967e-28
NZ_CP030771.1\|WP_138960904.1\|5177740_5179213_-\|ornithine-decarboxylase	gnl\|CDD\|99739	cd00615, Orn_deC_like, Ornithine decarboxylase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The major groups in this CD corresponds to ornithine decarboxylase (ODC), arginine decarboxylase (ADC) and lysine decarboxylase (LDC). ODC is a dodecamer composed of six homodimers and catalyzes the decarboxylation of tryptophan. ADC catalyzes the decarboxylation of arginine and LDC catalyzes the decarboxylation of lysine. Members of this family are widely found in all three forms of life.	3.9611e-115
NZ_CP030771.1\|WP_138966841.1\|5181351_5183130_-\|peptidoglycan-binding-protein	gnl\|CDD\|367272	pfam02956, TT_ORF1, TT viral orf 1. TT virus (TTV), isolated initially from a Japanese patient with hepatitis of unknown aetiology, has since been found to infect both healthy and diseased individuals and numerous prevalence studies have raised questions about its role in unexplained hepatitis. ORF1 is a large 750 residue protein. The N-terminal half of this protein corresponds to the capsid protein.	1.8818e-07
NZ_CP030771.1\|WP_138960907.1\|5183925_5185455_+\|HAMP-domain-containing-protein	gnl\|CDD\|182539	PRK10549, PRK10549, two-component system sensor histidine kinase BaeS.	2.85039e-46
NZ_CP030771.1\|WP_138960910.1\|5187564_5189142_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	3.73046e-07
NZ_CP030771.1\|WP_138960909.1\|5185966_5187568_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	1.48388e-08

>NZ_CP030771.1|WP_138960902.1|5172749_5174255_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MTATTAANGAPEAPDVPAASGVVAAPDAPAASGAGSAPVKGRSRRLALGVIATGMLMIILDGSIVTVAMPAMQEDLNFTPAGLSWVVNAYLIAFGSLLLLAGRLGDLIGRKRMFVTGIGLFTLASVLAGAATSPATLIAARFLQGVGGAMSSAVSLGILVTLFTEPGERARAIAVFSFTGAAGASLGQVLGGVLTDALNWHWIFFINLPIGLAALLLALPALPADRGLGLRAGADVTGALLVTAGLMTGIYSVVKVEQYGWASGHTLGFGGLAAVLLAGFVVRQTKARTPLLPLRMFRSRAVTGANVVQLLMVAALFSFQVLVALYLQNVLGYGAAETGLAMLPAAAVIGAVSLGVSARLNARFGERAVLLAGLVLLLGVLGLLTRVPVHATYWVDLLPVMLLAAGFGLALPALTSLAMSGARADDAGLASGLFNTTQQIGGALGVAVLSTLAASRTESLLATGHSRAEALTSGYHLAFGIGTALLAAAFLTAAALLRPAR
>NZ_CP030771.1|WP_138960901.1|5172075_5172561_-|winged-helix-DNA-binding-protein
MTAMAPTRTEPDLSFLLDHTSHVLRTQMAAALGEIGLTARMHCVLVHALQEERTQAQLAEIGDMDKTTMVVTVDALEKAGLAERRPAREDRRARVIAVTEKGAEVAARSQEIVDGVHERALGALSKTDRTALLRALNRLVEGHLATPAESPRPARRARQRA
>NZ_CP030771.1|WP_030688977.1|5171602_5171968_-|PH-domain-containing-protein
MALFGNAHTVDPASAQQEYARLMGHGEQVYAAYRLIRDTILLTDRRMIFVDKQGMTGKKVEYHSVPYRSITHFAVETAGHFDLDAELKIWISSNPVPIEKTFTKGVDIYEVQAILTQFVAR
>NZ_CP030771.1|WP_138960900.1|5171105_5171438_-|antibiotic-biosynthesis-monooxygenase
MIFITVKFTVRPERSEDWLDLVDDFTRATRAEPGNIFFEWSRSVDDPHQFVLVEAFRDGEAGREHVESAHFAAAMETMSYAIASTPQIVSTEIPGMDGWGAMGEVSPREA
>NZ_CP030771.1|WP_138960899.1|5170656_5171034_+|nuclear-transport-factor-2-family-protein
MPAQDVHETAVARYFEAWNATGTEDIRKAVEAAWTQDGTYTDPLADAAGTEALVAVIAAVQKQFPGFEFRRTGELDGHHGLVRFTWELVSGADGSAPVAGSDVAVLAEDGRVRTVYGFLDRLPQA
>NZ_CP030771.1|WP_138960898.1|5169419_5170442_-|SGNH/GDSL-hydrolase-family-protein
MRKQLVGGVVAGMLLLGACGDPGAEDGSGGAPAPDPPAASRTDGSGPPSQTNRQQAERDEEGDEERGKEGGASRAGPKSPGTSGGRASGPKPAPRVLYLGDSLAMENQDVLGSLLRDRLAARYTSAPYSGTTLCDYLEDTGEDSLVPDEDKAATLVRELRPDFVVLQFWGNSWGYTPCMGGVTYDKQRDTYFTRYAADARRLTGQIEEAARDVGAARPKVVWVSQGPDVMTPDRVRRVNELYRRQAAASGDLVSDAGRAVSPASARYRWVRELPCTADERAHPVYCTEPGGRTALHRGDDYLHFCLAPTTPKSRPCPVRSPGIRRIGQAVTDTVARAAKR
>NZ_CP030771.1|WP_138960897.1|5168563_5169400_+|hypothetical-protein
MTDELDLLRAADPVSATEGPWRDRPLDARAERGLNQLLHTSRRRARRRVVLWAEAAAVALAAVLVLTLPDLAATSATAAPRALHPRAGSAAVPLAEVAERARAAARDGEPGLRRGSHVRTWSLPAESGPRAEPPARPPGARARPPHTPAGLRAYLTDAYDRGAHRRSGPLTTDQLLDALPRLLDTWTLGARESAALARVLADTEGLRPAGAITDRLGRSGQAYVHRSRGAGDDELRRMLILDPGTGTVLGLEVMFTKAEPRFEVRAGDVRSYSAWRRD
>NZ_CP030771.1|WP_138960896.1|5168034_5168571_+|sigma-70-family-RNA-polymerase-sigma-factor
MSTDEAFAAAYREHYWAVSRFVARRLGAGETHEVEEVVAEVFSIAWRRRAELPENALPWLYGVARNCLANTVRGLGRYRRLLHRIGHHEATRHGQVVTGPDADAPGAWVHEALARLSPADQEALRLTTWEELGVDDLAVALGCGRSAAAMRLHRARRRLRAEIDRMRMNVTAGDGTHD
>NZ_CP030771.1|WP_138960895.1|5166299_5167928_-|cytochrome-c-oxidase-subunit-I
MRATVKWLTTTDHKTIGTLYLVTAFAFFCIGGVMALFMRAELARPGLQIMSNEQFNQAFTMHGTLMLLMFATPLFAGFANWLMPLQIGAPDVAFPRLNMFAYWLYLFGSLIAVGGFLTPGGAADFGWTAYAPITDAAHATNIGADMWIMGLALSGFGTILGAVNFITTIVCMRAPGMTMFRMPIFTWNVLLTGVLVLLAFPVLAAALFALEVDRKFGAHIFDVANGGALLWQHLFWFFGHPEVYIIALPFFGIISEVIPVFSRKPMFGYMGLIGATIAIAGLSVTVWAHHMYATGGVLLPFFSFMTFLIAVPTGVKFFNWIGTMWKGSLSFETPMLWAVGFLITFVFGGLTGVLLASPPMDFAVTDSYFVVAHFHYVIFGTVVFAMFSGFHFWWPKFTGKMLDERLGKITFWTLFIGFHGTFLVQHWLGAAGMQRRIPDYLDAEGFTGLNTLSTIFSFLLGMSLLPFFYNVWKTAKYGAYVEENDPWGYGRSLEWATTCPPPRHNFHSLPRIRSESPAFDLRHPEIAAELAPVPEPAERAAL
>NZ_CP030771.1|WP_138966837.1|5165952_5166294_-|hypothetical-protein
MDDRPAEAALLIHEIEGHLLVESARTESRAAAARFTARLDWLTQAQREEVERVYTEDHLALTRHIWRRTAHRSRELRTEYETRYRSLRRRLLAGALLGMTFALLVAGAWVSAP
>NZ_CP030771.1|WP_138960903.1|5176288_5176954_-|hypothetical-protein
MLSRIRGVLRREWQGVAVAAWRELRSRGAAGVALAVGGTLAMLVLHGLEQIPDPDRVVRMLGEVRADQPLWQSLLRTPLSVFIPTRDQPPWGGIPRLVLAFGLAQLLVGWRRTLLVAYGATLAGTLGARVMIAIGPGHWAGVPASYAHDVDTGASAAVVGLFTYLAVRLRAPVLCLAFVVPTVVGSLLNPNLAGREHLVAVALVAGVAAVRQGRGGLAGSG
>NZ_CP030771.1|WP_138960904.1|5177740_5179213_-|ornithine-decarboxylase
MEPIDHTAAPVLEALDAYHDRGRLAFTPPGHKQARGADPQARRVLGDAVFRSDVLAVGGLDDRRASGHVLSRAERLMADAVHAEHTYFTTCGSSLSVKAAMLTVAHPGDRLLIGRDAHKSVVAGLILCGIDPVWVEPQWDAERSLAHPPSVASYAAALDRHPDARGALVTSPTPYGSCADLRGLAELCHGRGLPLVVDEAWGAHLPFHEDLPSWAMDAGADICVTSIHKMGSGLEQGSVFHLQGNRVDPAELASRADLLGTTSPSVLIYAGLDAWRRQMVLRGHELMSGALRLAAEVHEEIELIPGLHVNGRADLTGPGLAADLDPLPTVIDISGLGTTGYRAADWLREHHALTVHIGDHRRIGAQLTHADSRETVGPLLDALRDLSAHRAELADAPRVDVPSPAELRMEQVCLPRDAYFGAVESVPLDRAAGRVAAEMATPYPPGIPAALPGERLTEPVLAYLRSGHAAGMYIPDTADHTLRTLRVLKE
>NZ_CP030771.1|WP_138960905.1|5179391_5180597_-|ABC-transporter-permease
MSAPGRDRLRPARLSPADVLRVGSVGLRARRARVVLSSLGIAIGIATMVAVVGLSTSSRADLMQRLDRLGTNLLTAEAGKDASGQEVKLPKSAVAMVERIGPVRQATATANVDARIRRSAAVPEERSAPVTAQAARPDLLSALNTRVAKGGWLDRGRERLPVTVLGRIAAERLGITAPGEKIMMGDRYVVVVGILAPMELVPTLDRVALVGFPAAERYFGFDGHPTTVFERSTDAAVEDVRAVLARTVNPGDKGSVTVSRPSDALAAKTATDEGLTALMLGLGAVALLVGGVGVANTMVISVLERRTEIGLRRAIGATRGAVRIQFLTESLLLSAIGGVAGAGLGALATHGFALAQGWTPVVPPWSLAGGLAATLVTGVLAGLYPAARAARLRPTVALNAA
>NZ_CP030771.1|WP_171075815.1|5180593_5181355_-|ABC-transporter-ATP-binding-protein
MNPPTSRAAAARQDTAGPPGAAVVELRRATKVYPGGVTALREVDLTVHDGELLAIVGPSGSGKSTALNLIGTLDRPTSGSVRVAGHDVGALSDAQVAALRARHIGFVFQHFHLAPGRSALDNVADGLLYAGVPARRRRAAAAEALERVRLGHRLGHRPGELSGGEKQRVAIARALVGAPRLLLADEPTGALDSASGQVVMELLRELNAAGTTVCVITHDHDIADSLPRRVRFRDGEIVFRDGEADFRGGEVVV
>NZ_CP030771.1|WP_138966841.1|5181351_5183130_-|peptidoglycan-binding-protein
MWPPDGEAHDHHLTQGAGLRRTPAPARRARRGPRARALRRLRLGLRRRRRRRRRRQAGPGRLRARVPRQGGRRRQGQGLGGPVRRGQGGQERLLRRADDVRPLHAHQSGAEGLSRPQAERLSQLARDRQDRRPQRRRRGVQGRQGRRLRRRAPRGDEPGAQARPAAGLRVDARARQVHAGQGRLAVPQPDDGRRQRAARRRARPHLTEARHEVPRLRGGPGGLRVQAARRPGRHAVRRRTGWLAAAGAAAAGVVTAGAFAVGGGQRDGAADEGGAPPATAEVVRTDLVLSKTVDGTVDFAGRRPVKPAVQGTVTVAAREGATVRQGQALYELDDKPVTLLYGPVPVFRGMKQGDRGTDVLQLERNLRDLGYGAGLYVDVRYDAATAAAVKRWQRSLNRVPTGRVGKGEVVFQGGPVKVVAADAALGDQVGPDAAVLTAASPTPVVRAGLDQGDGSLAARGTRAEIRLAGGKKVRGKVTGTVRPERTEDSGPGGDGITVEIALDGGAAALLGEAARATASVTFVSESRRGVLAVPVEALVALRGESGGYGLQLVPASGPPRMIRVGTGMTADGRIEVRGAGLREGVRVGVAAQ
>NZ_CP030771.1|WP_138960906.1|5183239_5183929_+|response-regulator
MPHVLLIEDDASVRDGMELVLRRHGYEVSAAATGEAALALLDGPGGEAVDIAVLDLMLPGLDGFEVCRRVRARASRPTLPVIMLTARGDDTDVVRGLEAGADDYVVKPVTAPVLEARIRAALRRATPVAARDTYAGLVVDRAGLTVTKSGTPLALPPTELRLLLELSASPGQVFSREQLLRSVWDHDFLGDSRIVDAAVGRLRAKIEDVASRPRYVQTVRGFGYRFGPL
>NZ_CP030771.1|WP_138960907.1|5183925_5185455_+|HAMP-domain-containing-protein
MKRPGRRPGSPGRRPERPGRRPGRLRAPRGLRTRLVVTFVLVALIGTATATALAYREARTAVLSRTQEAAQQDLRTRVDALAPDVDVPPDQRSLGVFARSVSSGLPGSPLVVARYENLKAASDGSPDDPRVTAGLRADVRVSGRMSFQRVTHEGEPYLAVGTPVTYEGGRASRLEVFAVTPLRAEERDVAALLTSVRDGLLPVLVLTAVLALLAARTVLRPVRDLGRATRRLADGDLGTRVEPRGRDELADLARDFNTTADALQTTVAELRDQEAKAREQEARARRFVADVSHELRTPLAAMTMVATVLDEDADRLPPDAAHAARTVSAETAKLTRLVDDLMEMSRFDAGVARLRLTEADLAATVRSSLALRAWTGRVTAELPDSAPALIDVRRIDVVVANLVGNALRHGAPPVTVRLTTGAGLATVTVTDHGPGLAPDALAHVFDRFYKADAARTRSEGSGLGTAIALENARLHGGTIEAANGPGGRGAVFTLRLPLRPAAGPGDGPR
>NZ_CP030771.1|WP_138960908.1|5185451_5185970_+|hypothetical-protein
MTPARAAALALALALAAALTACGVRPTGVVTGADPATGLTRGLRLYFVDGTGLRGVSRPEAKIRDLAGAVKLLGAGPNRTERESGLTNLVEIGRIDVTGRGDRVTYRSPGSFFDADSDRLPNGQLVCTLARAQSYLSSKDEDRRVRPDDVQVTLDNGERRFGPYRCSQFLDG
>NZ_CP030771.1|WP_138960909.1|5185966_5187568_-|PQQ-binding-like-beta-propeller-repeat-protein
MTQPPPGPPGPQGQFGPPPQAGFGPPVPLPPAGFGPPVEPPPGGFGPPAPVGPPPPRARRRRVVVIASVAALALVAGGGAWYVAARGDGPDGGGSKGGGKKPGPAYAKPAEVVPADPKATFHGGAPVPKLPKKESTWPVKGSWLTDEVYVKSSVAKITGLDAATGETRWTLPKPGQSCGGSPEIGAGGIAVVVVAPTTHDAKGFRAPCTQVLAFRVATGEKLWTKTVRIGYQTEKTPFNQVAISGRTVAVGGLYGGAAFDLRTGEPRWKPRAGDTCRDVGYGGGARLVAIRTCGDYGAEKYEVQDLDPRSGKPRWRYKLPGGVRNLNVVSTDPVVVGLDSGEITAHGASDVFALDGRGRLRSRISLPERQYAHDCGDTAVVNDCRGLVVGNDRLYAPTARRDAKDGIASTNDIVVFSLATGKTTGQRGNTDSNGPTFPFRMDGGNVLAYRDQLGVQVVTLDGRTLRERKLLTSAKRPGGLVPVESELHFVDGRLYMSTDLAFTSGAKGPERFMMYVFARKDQKDRKDQKDRKG
>NZ_CP030771.1|WP_138960910.1|5187564_5189142_-|PQQ-binding-like-beta-propeller-repeat-protein
MAGPPPQRPHEPVPGNPYVDPVPAPRRRGSATAWIAAGAVLAAVGAGAGAYALLKEDGGKGSGGFRAPLARDRGPSGEPSGSGERTDAPGGSGPPVRRIDVNAGAKPGESRGWLDLNGVRLPGKGAMLGDLWTVGGRSDALVVQALYDTVTAYRARDGEKAWTLRLPDKVCDTPVDTAPGGHVVVAYGDGSTSGTGKCNQLQQIDLRTGERGWHRELKEHDLSDSTSSVRLAVTGATVTVAQGDLAHTYRVSDGKRLFSSQRDRVGTCYLRDVAGGARLLYVENCAAGAPKAHGRVRNVDPRTGDVRWQYRSRDGWTVDKVYSVDPLVLAVRSRDDPDEWGIVSVDGKGRERAWIPLHRGPYAFEMCDGAGDAGEGVQNCPGGAVVGDVLHLPTAPKGGLGPNKVVAFDLATGKRRWAAAVPGGRQLTPVRQAGGGKGSGVVVYVRAQAGKPGRTVRFPASGGAPRVLLRHSTPAQKWEAEMFAGETLYSGGRVFVAPSRLAPKSLGGNKEQGRLLSFGGDLETP

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_10

5475781-5475921

Orphan

Consensus_repeat	Method
GCGCTTCGCGTCGGGGCCGGGCCTCGTGAGGCCGGGGAGTT	CRISPRCasFinder

1 spacers

csa3

The CRISPR arrays of NZ_CP030771_10

>merge|NZ_CP030771|10|5475781-5475921|CRISPRCasFinder
GCGCTTCGCGTCGGGGCCGGGCCTCGTGAGGCCGGGGAGTTCCGGGTGGGAGGGTGGGAAGCTCCGCCGCGGTAGCGGCGGTGCCGCCCACTCGGCGGCGGCGCTTCGCGTCGGGGCCGGGCCTCGTGAGGCCGGGGAGTT

>NZ_CP030771|10|9|5475781-5475921|CRISPRCasFinder
GCGCTTCGCGTCGGGGCCGGGCCTCGTGAGGCCGGGGAGTT	CCGGGTGGGAGGGTGGGAAGCTCCGCCGCGGTAGCGGCGGTGCCGCCCACTCGGCGGCG
GCGCTTCGCGTCGGGGCCGGGCCTCGTGAGGCCGGGGAGTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138961113.1\|5480210_5481413_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP030771.1\|WP_138966889.1\|5477969_5479112_+\|NADH-quinone-oxidoreductase-subunit-D	unknown	unknown	gnl\|CDD\|223722
NZ_CP030771.1\|WP_138961118.1\|5485271_5486270_+\|DUF2520-domain-containing-protein	unknown	unknown	gnl\|CDD\|227782
NZ_CP030771.1\|WP_138961103.1\|5467169_5468987_-\|DUF2156-domain-containing-protein	unknown	unknown	gnl\|CDD\|235095
NZ_CP030771.1\|WP_138966885.1\|5465628_5466237_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|379209
NZ_CP030771.1\|WP_138961116.1\|5483676_5483913_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961104.1\|5469267_5470401_+\|esterase	unknown	unknown	gnl\|CDD\|223700
NZ_CP030771.1\|WP_138961102.1\|5466254_5467139_-\|dihydropteroate-synthase	unknown	unknown	gnl\|CDD\|238380
NZ_CP030771.1\|WP_138961112.1\|5479076_5480105_-\|SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|224481
NZ_CP030771.1\|WP_138961110.1\|5474661_5475735_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961109.1\|5473539_5474502_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270324
NZ_CP030771.1\|WP_138961105.1\|5470584_5471742_-\|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213262
NZ_CP030771.1\|WP_138961108.1\|5472787_5473468_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224095
NZ_CP030771.1\|WP_138961101.1\|5465092_5465452_-\|dihydroneopterin-aldolase	unknown	unknown	gnl\|CDD\|376737
NZ_CP030771.1\|WP_171076112.1\|5475987_5477358_-\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|225962
NZ_CP030771.1\|WP_138961111.1\|5477342_5477855_-\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|225937
NZ_CP030771.1\|WP_138961114.1\|5481562_5482237_+\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP030771.1\|WP_138961106.1\|5472050_5472791_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224095
NZ_CP030771.1\|WP_138961115.1\|5482271_5483381_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|238042
NZ_CP030771.1\|WP_138961117.1\|5483872_5485135_-\|threonine-aldolase	unknown	unknown	gnl\|CDD\|224919

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138961113.1\|5480210_5481413_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.20577e-47
NZ_CP030771.1\|WP_138966889.1\|5477969_5479112_+\|NADH-quinone-oxidoreductase-subunit-D	gnl\|CDD\|223722	COG0649, NuoD, NADH:ubiquinone oxidoreductase 49 kD subunit 7 [Energy production and conversion].	8.41208e-147
NZ_CP030771.1\|WP_138961118.1\|5485271_5486270_+\|DUF2520-domain-containing-protein	gnl\|CDD\|227782	COG5495, COG5495, Uncharacterized conserved protein [Function unknown].	1.91477e-53
NZ_CP030771.1\|WP_138966885.1\|5465628_5466237_-\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|379209	pfam13474, SnoaL_3, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	8.06281e-21
NZ_CP030771.1\|WP_138961111.1\|5477342_5477855_-\|PH-domain-containing-protein	gnl\|CDD\|225937	COG3402, COG3402, Uncharacterized conserved protein [Function unknown].	6.32486e-24
NZ_CP030771.1\|WP_138961108.1\|5472787_5473468_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224095	COG1174, OpuBB, ABC-type proline/glycine betaine transport systems, permease component [Amino acid transport and metabolism].	1.56642e-54
NZ_CP030771.1\|WP_138961102.1\|5466254_5467139_-\|dihydropteroate-synthase	gnl\|CDD\|238380	cd00739, DHPS, DHPS subgroup of Pterin binding enzymes. DHPS (dihydropteroate synthase), a functional homodimer, catalyzes the condensation of p-aminobenzoic acid (pABA) in the de novo biosynthesis of folate, which is an essential cofactor in both nucleic acid and protein biosynthesis. Prokaryotes (and some lower eukaryotes) must synthesize folate de novo, while higher eukaryotes are able to utilize dietary folate and therefore lack DHPS. Sulfonamide drugs, which are substrate analogs of pABA, target DHPS.	2.38077e-113
NZ_CP030771.1\|WP_138961112.1\|5479076_5480105_-\|SAM-dependent-methyltransferase	gnl\|CDD\|224481	COG1565, COG1565, Uncharacterized conserved protein [Function unknown].	3.20856e-22
NZ_CP030771.1\|WP_138961103.1\|5467169_5468987_-\|DUF2156-domain-containing-protein	gnl\|CDD\|235095	PRK02983, lysS, bifunctional lysylphosphatidylglycerol synthetase/lysine--tRNA ligase LysX.	0
NZ_CP030771.1\|WP_138961104.1\|5469267_5470401_+\|esterase	gnl\|CDD\|223700	COG0627, COG0627, Predicted esterase [General function prediction only].	5.69059e-10
NZ_CP030771.1\|WP_138961105.1\|5470584_5471742_-\|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein	gnl\|CDD\|213262	cd03295, ABC_OpuCA_Osmoprotection, ATP-binding cassette domain of the osmoprotectant transporter. OpuCA is a the ATP binding component of a bacterial solute transporter that serves a protective role to cells growing in a hyperosmolar environment. ABC (ATP-binding cassette) transporter nucleotide-binding domain; ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition, to the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	7.06385e-150
NZ_CP030771.1\|WP_138961101.1\|5465092_5465452_-\|dihydroneopterin-aldolase	gnl\|CDD\|376737	pfam02152, FolB, Dihydroneopterin aldolase. This enzyme EC:4.1.2.25 catalyzes the conversion of 7,8-dihydroneopterin to 6-hydroxymethyl-7,8-dihydropterin in the biosynthetic pathway of tetrahydrofolate.	9.10216e-44
NZ_CP030771.1\|WP_171076112.1\|5475987_5477358_-\|PH-domain-containing-protein	gnl\|CDD\|225962	COG3428, COG3428, Predicted membrane protein [Function unknown].	3.87006e-35
NZ_CP030771.1\|WP_138961109.1\|5473539_5474502_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|270324	cd13606, PBP2_ProX_like, Bacterial substrate-binding protein ProX of ABC-type osmoregulated transporter and its related proteins; the type 2 periplasmic-binding protein fold. This group includes periplasmic substrate-binding component of ABC transport systems from gram-negative and -positive bacteria that are involved in uptake of osmoprotectants (also termed compatible solutes) such as betaine, choline, proline betaine, carnitine, and L-proline. To counteract the efflux of water, many microorganisms accumulate the compatible solutes for a sustained adjustment to high osmolarity surroundings. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.25717e-89
NZ_CP030771.1\|WP_138961114.1\|5481562_5482237_+\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.43519e-73
NZ_CP030771.1\|WP_138961106.1\|5472050_5472791_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224095	COG1174, OpuBB, ABC-type proline/glycine betaine transport systems, permease component [Amino acid transport and metabolism].	2.72556e-55
NZ_CP030771.1\|WP_138961115.1\|5482271_5483381_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	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.	5.05674e-13
NZ_CP030771.1\|WP_138961117.1\|5483872_5485135_-\|threonine-aldolase	gnl\|CDD\|224919	COG2008, GLY1, Threonine aldolase [Amino acid transport and metabolism].	3.29418e-41

>NZ_CP030771.1|WP_138961110.1|5474661_5475735_+|hypothetical-protein
MPRGRHRHSPPLHRLLPPSAVAGFSLAAAGGAWLFAEPVVLRGLAAAAAASAVLGSVVMRRWDRAAGKRVAELGRARASEEWRYEERIAECESDLDEARELRSKLENKLRSKRAELAALRNEHAALLRRYATAETERASALEGRRLLAIEATTSTRALPAGSAEDAEEDTPEASLYERANAALDRLTGRHGEAEAEIEVEVEVEAVEDLDASDAPEAEADDKELSAPEAAEAADEPEAADEAVDGHERAAGAHLLVPAAAAVVPPAQARRTAGEGGFDFFGTKGAAPAALDAVQNEDLADVVGEEALAVHKAEAEAEFKPSDATTDAERGVGQVIDLTAHDETEQIDLKGLRTALRA
>NZ_CP030771.1|WP_138961109.1|5473539_5474502_+|ABC-transporter-substrate-binding-protein
MNSRTRRARRMAGTAVAVVTLGAGLAACGGDSLEDDKDSVGGKGAIVVGSARFTEQKVLAELYAGVLRDAGYDASVKTVQNREVYEPELKKGSIDVAPEYAATLTEFLNLKKNGSDAEPVASSDLGATVSELAKLAKPRGLKALPAGGAVDQNAFAVTKDYAKEHKLKTLSDLGKSGEKVRIAAGDECETRPFCAPGLKKKYGIDVAGIDPKGVGTTQSKQAVKNGTDQLVLTTTTDATLKNFGLVILEDDKKLQNADNILPVVNEKSAGDKEIADALGKLTKTLTTDDLIELNRKVDEERQKEGDVAKDYLKSKGLIEK
>NZ_CP030771.1|WP_138961108.1|5472787_5473468_+|ABC-transporter-permease-subunit
MNAISGAYEWLTTSANWQGEKGVWHRLAEHLYFSGVCLAVSCAIALPIALLLGHIGKGGALAVNISNVGRAVPTLAVLILLTLTPLGEHGDVPTLIALVLFAVPPLLTNAYVGMREVDRSVVEAARGMGMSGRQVFGRVELPLAYPLIMTGVRSAAVQVVATATLAAMAGEGGLGRIITAGFNLQNTPQVVAGAFLVALLALAVEGVLVAVGWACDPMRGRSRMRA
>NZ_CP030771.1|WP_138961106.1|5472050_5472791_+|ABC-transporter-permease-subunit
MSKRNCLVTNDWICGEYVRSRSQELIDATVQHVGITAASVAIGVAVSLPLALLARRWRFLAAPILGVTTVLYSIPSLAMFSLLLPFFGLSASLVVTGLVLYSLTILVRNILAGLRAVPEEAREAAKGMGYGPLRLLWEVELPLALPSLLAGVRITTVSTVALTTVGAIVDKGGLGTMILDGLDTQFKAQVLTASVLCVLLALAADLLLLALQRWLTPWTRAHRIRTSRFSRKADAAPGVGKVAEPV
>NZ_CP030771.1|WP_138961105.1|5470584_5471742_-|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein
MIRFEHVTKRYADGTTAVDDLSFEVNEGELVTLVGPSGCGKTTTMKMVNRLIEPTSGRIFLDGDDISDIDPVQLRRRIGYVIQQVGLFPHKTVLDNTATVPHLLGVKRAKARERAAELLDLVGLDPAVYGDRYPEQLSGGQRQRVGVARALAADPPVLLMDEPFGAVDPVVRERLQNEFLRLQQAVRKTVLFVTHDIEEAVRLGDRIAVYGHGRIEQFDTPSTVLGAPATEYVADFVGADRGLKRLSVTPIEEGDLEQPPVVHLDDALPRELDARWAVVLDGDNNLHGWISAEHARGGTGTVREHARRMEAWLPVGASLKQAFSTMLQHDAGWIAVIDEHSEGRFLGVLTPARLHEALRRSTTADALDIARGDVELESVATVTGG
>NZ_CP030771.1|WP_138961104.1|5469267_5470401_+|esterase
MGLTSNKVLALAIALAVLLFIGTIWLWPRLARRSWRAITGRVGLLLATQVAVFASIGLYTNQAFGFYASWADLLGQETEQGVVVDHDVLKGEKGPVKVTDTQTVDVPGGETPRVGGQIQKVQVQGRNSKIASPAYVYLPPEYFQPQYKHRTFPSAVVLTGYPGTAEALIKGLHYPQTAHKQVRQGKMQPMILVMLRPTVAPPRDTECVDIPGGPQAETFFARDLPDAITQHYRAGKKPDSWGIIGDSTGGYCALKLAMHHPDVYGAGASLSGYYKAAQDVTTGNLFHGDKDLENQANLMWYLDHMPPPKTSLLLSSSKKGEGNYKDTLKFIDKVKPPTRVSSMILDSGGHNFNTWRREIPGSLVWMSERLTGGSDVR
>NZ_CP030771.1|WP_138961103.1|5467169_5468987_-|DUF2156-domain-containing-protein
MSGVVPEGKGGLRRILRGPRPEAVPTLVARACTLVGLLNVAAGVFPRFRHSRLHTFAEVLPGLFGPFAAALALSCGVLLLLLAHGLRRNKRRAWRAAVVLLPLGAVAQFTYRHSFIGVLIPIALLVLLLRHRKEFAALPDPRSRWRALANFVVLGAGSLALGLVIVSVHPDKVVGDPSISERLMHVLYGLFGVEGPVDYTGRTPWTVGFSLGALGLLTALTTIYLAFRPEHPAARLTEDDETRLRELLAKHGGRDSLGHFALRRDKGVVFSPSGKAAVTYRVVSGVMLASGDPIGDVEAWPGAIERFMDEAKAHSWTPAVMGCSETGGQVWTRETGLDALELGDEAVVEVADFSLSGRAMRNVRQMVKRIERNGYETRVRRIRDLGEQELERIQRAADDWRGTDTERGFSMALGRIGDPSDGDCLIATAHKTDEQPGPYGDLKAVLHFVPWGKDGVSLDLMRRDRSADPGMNELLIVAALQAAPQLGIARMSLNFAMFRAALARGEKLGAGPVLRAWRGLLVFLSRWFQIESLYKFNAKFQPRWEPRFVVYRSSRDLPRIGFAAMQAEGFVTLALPRFLRRRTAGPRPCPHQSVRSAEQHEVRAA
>NZ_CP030771.1|WP_138961102.1|5466254_5467139_-|dihydropteroate-synthase
MSTLRGRGSVEGLPQWDRCAVMGVVNVTPDSFSDGGRWFDTTAAVKHGVDLVAQGADLVDVGGESTRPGAPRVDEDEELRRVVPVVRDLAAEGVTVSVDTMRATVARQALAAGAVLVNDVSGGLADPDMVPSVAAAGAPFVVMHWRGFLTDMHAKPVYEDVVSEVVDEIHARVEAAIAGGIAPERIVVDPGLGFSKDAEHDLALVAHLERLRDLGRPVLVAASRKRFLGRVLAGPGGSPPPARERDAATAAVSAIAAHQGAWAVRVHEVRATADAVRVAQAVTDAGSAGAAGAR
>NZ_CP030771.1|WP_138966885.1|5465628_5466237_-|nuclear-transport-factor-2-family-protein
MEQVERANTAFYEALERGDFDAVTDLWLDPADLADGTGSGGPSSLTSALSRLPVDLEDDEDPGAPDGTDDDSRDGGADGFGEDADDGAAISCVHPGWPVLTGRGEVLRSYALIMANTEYIQFFLTDVRVSVAGDTALVSCTENILSGGPAPREGDELGPLVGQLVVATNVFRRTSDGWKLWSHHASPVLAESGDDEDDESPS
>NZ_CP030771.1|WP_138961101.1|5465092_5465452_-|dihydroneopterin-aldolase
MDRVALRGLKARGHHGVFPREREEGQTFIVDLVLGLDTRAAAADDDLAKTVHYGIVAEEVVAVVEGEPVNLIETLSERIAQACLKHDGVLEVEVTVHKPDAPITVPFDDVTVTITRSRV
>NZ_CP030771.1|WP_171076112.1|5475987_5477358_-|PH-domain-containing-protein
MGGAVTGEPAAGPRAEAAPEPQAGGDGPVERRLHPVTPLRRAWAPVAVLMGWAFHDPDGAQRRMADMTATSLALVATAVVVGGSLYGFLSWWYTHYAVTDTELRIRTGLVFRRTAHIRLDRLQAVDLTQPLVARVAGVSKLKLDVVGTDKKDELAYLGERDATALRAELLARAAGFAPETAHEVGEAPSRQLLHVPPRMLAVSVLLTGAPWLLLLATLVVPTVLWFLTHSVWTVIVTGLPMLGGAFASSVGRFVGEYDWTVGESPDGLRLDHGLLDKAHETVPPGRVQSVRLVEPLLWRRFGWVRVELDVAGSANGVLVPVAPRALAESVIAQVLPGVRVPGPDELSRPPARASWCVPVWWKGHGLAVTDAVFAARHGLLRRRLSLVPHAKVQSVRLVQGPWERFKGVADVKVDTGAGRTVTARLRPSGEAAELLRGQAERSRTGRRAARPDRWMA
>NZ_CP030771.1|WP_138961111.1|5477342_5477855_-|PH-domain-containing-protein
METGTGAPGTAPGADAGEPVWTGLPRGLLKMRRMLLVVWLVPIAVALGVLLGLFAGPVWAVLAALPLALAAWGWVLLERNWRSWRYAERVDDLLISRGVLWREETVVPYGRMQLVEVTSGPVERYFGLAGVQLHTAAAATDARIPGLEPQEAERLRDRLTELGEARSAGL
>NZ_CP030771.1|WP_138966889.1|5477969_5479112_+|NADH-quinone-oxidoreductase-subunit-D
MTETTVGVGGAAESTDMVLNIGPQHPSTHGVLRLRLVLDGERIQHAEPVIGYMHRGAEKLFEARDYRQIVMLANRHDWLSAFSNELGVVLAVERMLGMEVPERAVWTRTLLAELNRVLNHLMFLGSYPLELGGITPVFYAFREREELQNVMEEISGGRMHYMFNRVGGLKEDLPAGWTARARAAVASVRSRMDVYDRLVLGNEIFRGRTRGVGVLSEEAVHAYGVSGPIARASGVDFDLRRDEPYLAYGELGDVLKVVTREEGDCLARFECLLEQTHNALDLADACLDRIADLPQGPINQRLPKVLKAPEGHTYAWTENPLGINGYYLVSKGEKTPYRLKLRSASYNNIQALTELLPGQLVADMVAILGSLFFVVGDIDK
>NZ_CP030771.1|WP_138961112.1|5479076_5480105_-|SAM-dependent-methyltransferase
MTHEAQRAAGHPARGWREATEEALYGPYGFYRRPEGPAGHFRTSVHASPLYAAAVARLLRRVDAALGHPRELAFVDVGAGRGELTTGVLAELPADVAARTRAYAVERAARPEGLDPRVRWCAAPPAGTSGLLFANEWLDNVPLDVAETAPDGSVRQVLVHEDGAEELGGPLAGPDADWLARWWPLGPEPGLRAEIGRPRDAAWAAAVATLDRGLAVAVDYAHTRDARPPFGTLTGFREGRETVPVPDGGCDITAHVALDACALPGGRLLTQRAALAALGVRGGRPPLALASADPAAYVRALTRAGEAAELTARGGLGDFGWLTQPVGIPDPLLVDVADHEEQ
>NZ_CP030771.1|WP_138961113.1|5480210_5481413_+|sensor-histidine-kinase
MQRLYDFLRRHPTGVDAFWAFVLLGLSGLSVVAVADSDGHDPTLVVIPVVIGLCLVVALRRRFTEHMLVLAAVIGLVQMAGDVRPNMANFAMLVIIYTAAADGPKWASRFALTGGLAAAPLSQLRWPETSAGMWGKVLYTVFMIVPFALAWVLGDSIRTRRAYLAQLEERAARLEKEREAQAKVAVAAERARIARELHDVVAHNVSVMVVQADGAAYVLDAAPDQAKQALATISGTGRQALAEMRRLLGVLRTGEHEESGEYVPQPDVEQLDELIEQVRGAGLPVDFKVEGTPRPLPSGVELTAYRIVQEALTNTRKHGGENAGASVRLVYFDDGLGLLVEDDGKGAPHELYEDGGADGSGHGLIGMRERVGMVGGTLDAGPRPGGGFRISALLPLKPAH
>NZ_CP030771.1|WP_138961114.1|5481562_5482237_+|response-regulator
MSIRVMLVDDQVLLRTGFRMVLAAQPDMEVVAEAGDGVEALQVLRATAVDVVLMDVRMPKLDGVETTRRICSEANPPKVLILTTFDLDEYAFSGLKAGASGFMLKDVPPGELLAAIRAVHSGDAVVAPSTTRRLLDRFAPMLPGTAGQPQHKGLERLTEREREVMVLVAQGLSNGEIAARLVLSEATVKTHVGRILTKLGLRDRVQVVVLAYETGLVRAGGGGG
>NZ_CP030771.1|WP_138961115.1|5482271_5483381_-|metalloregulator-ArsR/SmtB-family-transcription-factor
MSVSIDITGLAPERVHVVPSPLAELGMALHALSEPGHHPGLQGWATAVNARLDQSLADRLCEADFLWRTTFSDVFAPFAGIPGKRALPGATLAEELDQLDKLTDEQFVDAALEFTCQLAYDQNRVTDPLNDPKMRRHALELAAARGEHQVAFTERLLDDPPAVRAWFRQLMQDCDEAFFSDTWARLSHQLAADARHKTELLRRKGLGEALKAMSGAVTLDEEARRITVDKMASGHTRTAEGGLVLVPTSLGWPHVMVLHRYGWQSSITYPIRSPGLTEPASVEQLTRRMAALSHPVRMRLCRHLARGAYTTGELADAHGMTAPEISRHLSVLKKAELITTRRRGRYVQHQLDLGVVSRLGSEFIEGVLR
>NZ_CP030771.1|WP_138961116.1|5483676_5483913_+|hypothetical-protein
MSVTQQFLLDSYRAAQHGEAAPPAPGAHDWQVVREVRDYGRFHAVVHERPAHGRLRAALRRALHGLRGGAVRSPRPLP
>NZ_CP030771.1|WP_138961117.1|5483872_5485135_-|threonine-aldolase
MTAHDAQDDAPTPQESPPAAGPESPRAAGPETPQEDPGAAGPEGRGEPDERERRIAAARGARRLLARPPVTVPLGEHLAALAAGAADVADLQGPADLYGDGVVEDLEDEVARLLGKEAAAFFPTGTMAQQVALRCWAGRTGNATVALHPRSHPEVHERDALVTVSGLRTAHPTDAPRPPTAEEVRDFEEPFGTLMLELPLREPGFLLPTWDELQEVVAAARERDAVVHFDGARLWECAPHFGRPLDEIAGLADSVYVSFYKSLEGIAGAALAGPQTLVEEARAWRHRYGGLGFQQFPTALSALLGLRNVLPRLPEYVAHARVVADALRGAFEASGVPWSRVHPQPPHTHQFQVWLPYPPDVLNEAALAQAEETKTLLFWRWFPDGPPGLSVTEVTVAGPGLAWTADDVREAVADFVRRLP
>NZ_CP030771.1|WP_138961118.1|5485271_5486270_+|DUF2520-domain-containing-protein
MNAPHRPEPHSDPRAGHGPDPKDRPARLTVGVVGAGRVGPALAAALQLAGHRPVAVSGVSDSSVRRAAAMLPDVPVVTPAQVLERADLVLLTVPDDALPGLVEGLAETGAVRPGQLLAHTSGRYGTKILDPALRAGALPLALHPAMTFTGTPVDVQRLAGCSFGVTAPDELRLAAEALVIEMGGEPEWIAEDARPLYHAALALGANHLVTLVAESMELLRGAGVAAPDRMLGPLLGAALDNALRSGDAALTGPVARGDAGTVAAHVAELRKHAPQTVAGYLAMARATADRALAHGLLKPELAEDLLGVLAGPGGAAGGTEGFRDGGADGGDR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_11

5507925-5508015

Orphan

Consensus_repeat	Method
CCCCACCCGCCCGCCCTTCTCAG	CRISPRCasFinder

1 spacers

PD-DExK

The CRISPR arrays of NZ_CP030771_11

>merge|NZ_CP030771|11|5507925-5508015|CRISPRCasFinder
CCCCACCCGCCCGCCCTTCATCAGCCAGACCCCGGCTCCGTCCCGGCGGGTTCCGCTGTGCGCCGGCTCTTTCCCCGCCCGCCCTTCACAG

>NZ_CP030771|11|10|5507925-5508015|CRISPRCasFinder
CCCCACCCGCCCGCCCTTCATCA	GCCAGACCCCGGCTCCGTCCCGGCGGGTTCCGCTGTGCGCCGGCT
CTTTCCCCGCCCGCCCTTCACAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138961129.1\|5502771_5504181_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP030771.1\|WP_138961127.1\|5499315_5499873_+\|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl\|CDD\|366703
NZ_CP030771.1\|WP_138961132.1\|5505733_5506273_-\|SigE-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|132028
NZ_CP030771.1\|WP_138966897.1\|5500729_5502217_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|129794
NZ_CP030771.1\|WP_138961138.1\|5515640_5517353_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274357
NZ_CP030771.1\|WP_138961134.1\|5509795_5510482_+\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP030771.1\|WP_138966899.1\|5508245_5509799_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|226951
NZ_CP030771.1\|WP_138961136.1\|5512742_5513867_-\|DNA-integrity-scanning-protein-DisA	unknown	unknown	gnl\|CDD\|237395
NZ_CP030771.1\|WP_138961125.1\|5495084_5497610_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|214361
NZ_CP030771.1\|WP_138961131.1\|5505059_5505674_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961140.1\|5519962_5520787_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138961137.1\|5513957_5515367_-\|DNA-repair-protein-RadA	unknown	unknown	gnl\|CDD\|236994
NZ_CP030771.1\|WP_138966901.1\|5517362_5518307_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961126.1\|5497692_5498670_-\|DUF1016-family-protein	PD-DExK	COG4804_PD-DExK_CAS-I:CAS-III	gnl\|CDD\|380007
NZ_CP030771.1\|WP_138961135.1\|5511826_5512660_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|164795
NZ_CP030771.1\|WP_138961128.1\|5499897_5500479_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP030771.1\|WP_138961133.1\|5506529_5507462_-\|A/G-specific-adenine-glycosylase	unknown	unknown	gnl\|CDD\|224115
NZ_CP030771.1\|WP_138961130.1\|5504258_5504972_-\|response-regulator	unknown	unknown	gnl\|CDD\|223816
NZ_CP030771.1\|WP_138961139.1\|5518444_5519377_+\|Ppx/GppA-family-phosphatase	unknown	unknown	gnl\|CDD\|223326
NZ_CP030771.1\|WP_138961141.1\|5520783_5521416_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380054

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138961129.1\|5502771_5504181_-\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.7399e-31
NZ_CP030771.1\|WP_138961127.1\|5499315_5499873_+\|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl\|CDD\|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	4.91624e-36
NZ_CP030771.1\|WP_138961132.1\|5505733_5506273_-\|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.	4.60706e-58
NZ_CP030771.1\|WP_138966897.1\|5500729_5502217_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	5.64854e-74
NZ_CP030771.1\|WP_138961138.1\|5515640_5517353_+\|hypothetical-protein	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	2.84917e-09
NZ_CP030771.1\|WP_138961134.1\|5509795_5510482_+\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.90068e-69
NZ_CP030771.1\|WP_138966899.1\|5508245_5509799_+\|ATP-binding-protein	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	6.14807e-25
NZ_CP030771.1\|WP_138961136.1\|5512742_5513867_-\|DNA-integrity-scanning-protein-DisA	gnl\|CDD\|237395	PRK13482, PRK13482, DNA integrity scanning protein DisA; Provisional.	0
NZ_CP030771.1\|WP_138961125.1\|5495084_5497610_+\|AAA-family-ATPase	gnl\|CDD\|214361	CHL00095, clpC, Clp protease ATP binding subunit.	0
NZ_CP030771.1\|WP_138961140.1\|5519962_5520787_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	9.53999e-29
NZ_CP030771.1\|WP_138961137.1\|5513957_5515367_-\|DNA-repair-protein-RadA	gnl\|CDD\|236994	PRK11823, PRK11823, DNA repair protein RadA; Provisional.	0
NZ_CP030771.1\|WP_138961126.1\|5497692_5498670_-\|DUF1016-family-protein	gnl\|CDD\|380007	pfam17761, DUF1016_N, DUF1016 N-terminal domain. This family may include an HTH domain.	9.20527e-44
NZ_CP030771.1\|WP_138961135.1\|5511826_5512660_+\|hypothetical-protein	gnl\|CDD\|164795	PHA00370, III, attachment protein.	2.60493e-06
NZ_CP030771.1\|WP_138961128.1\|5499897_5500479_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	1.70595e-16
NZ_CP030771.1\|WP_138961133.1\|5506529_5507462_-\|A/G-specific-adenine-glycosylase	gnl\|CDD\|224115	COG1194, MutY, A/G-specific DNA glycosylase [DNA replication, recombination, and repair].	1.80742e-79
NZ_CP030771.1\|WP_138961130.1\|5504258_5504972_-\|response-regulator	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.6544e-82
NZ_CP030771.1\|WP_138961139.1\|5518444_5519377_+\|Ppx/GppA-family-phosphatase	gnl\|CDD\|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	3.26053e-81
NZ_CP030771.1\|WP_138961141.1\|5520783_5521416_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|380054	pfam17920, TetR_C_16, 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. This entry represents the C-terminal domain found in a number of different TetR transcription regulator proteins found in Actinobacteria. 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.	8.14013e-32

>NZ_CP030771.1|WP_138961133.1|5506529_5507462_-|A/G-specific-adenine-glycosylase
MPTALAADRADSRAAEGPSSHGRLHSPVIAWFEAHARDLPWRRPDAGPWGVMVSEFMLQQTPVARVLPVYEQWVARWPRPADLAKEAPGEAVRAWGRLGYPRRALRLHGAAVAITERHGGDVPTQHAQLLALPGIGEYTAAAVASFAYGQRHAVLDTNVRRVFARAVTGVQYPPNATTAAERKLARALLPEDEATAARWAAASMELGALVCTAKNEDCGRCPIAAHCAWLTAGKPAHEGPARRGQTYAGTDRQVRGKLLAVLREAVTPVPQSALDRVWDEPVQRARALDGLVADGLVEPLPDGFYRLPLT
>NZ_CP030771.1|WP_138961132.1|5505733_5506273_-|SigE-family-RNA-polymerase-sigma-factor
MAHGEVLEFEEYVRTRQDALLRSARRLVPDPVDAQDLLQTALVRTYGRWDGIADKRLADAYLRRVMINTRTEWWRARKLEEVPTEQLPDASVDDSTEQHADRALLMDIMKVLAPKQRSVVVLRHWEQMSTEETAAALGMSAGTVKSTLHRALARLRQELESRDLDARVFEREERERCAA
>NZ_CP030771.1|WP_138961131.1|5505059_5505674_-|hypothetical-protein
MSPKAGSTAVAVLAALGLLLAVTSCSAGGSGTRDEGPARTGAVASASPSESPSPAPKNVDAVQLVKSDPKVSLAVKRDLKPCTEDEYPVDVSYGNLTGAASSDIVVNVLTCGDAVGIGSYVYRPDGKKYKNVFVDEQPPVYAEIDRGDLVVSKQLYGKDGSVAEPTGEDVITYRWATDHFTERGRVRNNYSSAVGGEPTPSSDN
>NZ_CP030771.1|WP_138961130.1|5504258_5504972_-|response-regulator
MAEHTHVLFVEDDDVIREATQLALERDGFVVTAMPDGLLGLDAFRADRPDIALLDVMVPGMDGVSLCRRIREESTVPVIMLSARADSIDVVLGLEAGADDYVTKPFDGAVLVARIRAVLRRFGHASGSGTGAAASQDQGPGDGGVLTFGDLEIDTEGMEVRRGGQPVALTPTEMRLLLEFSSAPGTVLSRDKLLERVWDYGWGGDTRVVDVHVQRLRTKVGQDRIETVRGFGYKLKA
>NZ_CP030771.1|WP_138961129.1|5502771_5504181_-|HAMP-domain-containing-protein
MSGAARRGRDARTGFGGRAGGLRDRLLGLVGTRLRTGVRWKIATAIGFVGALIAVALSLVVHNAARVSMLDNARDLQDERVQIAQRNYEARGTTTAIYGTKVDDPELPKELRRQVLKGRRATYVQERGGGTPDIWAAVPLSDGHVLSVHTRFTDRSATIMKDLDQALVIGSISVVFGGCAVGVLIGGQMARRLRKAATAAREVAQGQTEVSVRDAIGGVVRDETDELAQAVDAMADALKQRLEAERRVTADIAHELRTPVTGLLTAAELLPPGRPTELVKDRAQAMRTLVEDVLEVARLDSASERAELQDILLGEFVSRRMATLPVEVTVTVVHESEVTTDPRRLERILYNLVTNAAKHGKPPIEVSVEGRVVRVRDHGPGFPEALLAEGPSRFRTGSADRAGRGHGLGLTIAAGQARVLGARLTFRNVRPPGESTNGPAVGAVAVLWLPEHAPTNTGSYPMLQLPDLG
>NZ_CP030771.1|WP_138966897.1|5500729_5502217_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MRVVIFALMVAILLAMLDNMIVSPAMPTIVGDLGGLEHLSWVVTGYTLATAASTPIWGKLGDMYGRKGAFLTSIVIFLIGSALSGLAQDMGQLIAFRAVQGLGAGGLMVGVMAIIGELVPPRERGKYMGMMTGVMAVAMIGGPLVGGTLTDHLGWRWAFYINLPLGIVALFMVSAVLHLPKKQAGGRIDYLGAALLTVGITSFVLVTTWGGTEYAWDSAVIMELIGLGVASLVGFYFVQQKAAEPLMPLRIFRSRNFTLMSVISFLTGFVMFGAMLFLPLYQQAVQGASATNSGLLLMPMLLAMMAVSNVAGRVTTSTGKYKVFPIAGSVLMAVGLFLLAQMDTETSRLTSGIYMAVLGAGMGCLMQITMLVAQNSVEMKDMGVASSSATLFRTLGSSFGVAVMGALFNNRVQDEMAERAGAAGGKVTEQSAQLDAASLAKLPDVVRDAYQHAVSSGTHAAFVLGSVMAVAALCAAVFVRETPLRGSAPAAPADQ
>NZ_CP030771.1|WP_138961128.1|5499897_5500479_-|TetR-family-transcriptional-regulator
MGTGKQQRRGDTRQRIQDVALELFAEQGYEKTSLREIAERLEVTKAALYYHFKTKEDILTSIFDDMTRPIDELIEWGKEQPRTLDTKRAILTRYSEILTNAAPLFRFMQENQATMRDLKTGESFKDRMLQLLDILKSDDPATPMTAQVRCFSALFTMHGGMFVLKDAEGDPEEKRKAILEVAIDLVTQAHEGV
>NZ_CP030771.1|WP_138961127.1|5499315_5499873_+|peptidoglycan-DD-metalloendopeptidase-family-protein
MSKRSKSHPSGRPSCRVRAAVVAVGVGAVTALGAGAAGAAVKAPAAPSWQDPVDRYRLSATFGLGGSMWAHKHSGQDFAVPSGTVVKSVHAGTVVKAGPNGAGDGPAYGNAVVIKHANGTYSQYAHLSRVEVRVGQAVTGGQRIALSGNTGNSSGPHLHFEIRTTPNYGSAVDPVSFLRQQGVRV
>NZ_CP030771.1|WP_138961126.1|5497692_5498670_-|DUF1016-family-protein
MHKYEDLLAEAKATAEGARLRTRRAVNAELVQMYWRIGKLILARQTEDGWGTGIVARLATDLRGAFPRQRIFSYRNLVQTPKMAHTWPALIAQRPVAQLPWSHITVLLDKLHTRAERDFYATEAVRNGWSRAQLTLAIRQRLHLPQRATPPLPDDVTLPAGSPALAELACDPYRLDFLRLDDQRPADPTYEESIANRMVRVLTGLGSGFAFVGCRYPVLAGDQYHRVDLLFYHLSLRRYVACALGTTTTRPTHLTRLDAQVRAVDDLVRDPDRDAPTIGVLIETSSGQATYTSLPPRGRQLLPTEEDLARVLREAVAPADATPHL
>NZ_CP030771.1|WP_138961125.1|5495084_5497610_+|AAA-family-ATPase
MFERFTDRARRVVVLAQEEARMLNHNYIGTEHILLGLIHEGEGVAAKALESLGISLEAVRQQVEEIIGQGQQAPSGHIPFTPRAKKVLELSLREALQLGHNYIGTEHILLGLIREGEGVAAQVLVKLGADLNRVRQQVIQLLSGYQGKETATAGGPAEGTPSTSLVLDQFGRNLTQAARESKLDPVIGREKEIERVMQVLSRRTKNNPVLIGEPGVGKTAVVEGLAQAIVKGEVPETLKDKHLYTLDLGALVAGSRYRGDFEERLKKVLKEIRTRGDIILFIDELHTLVGAGAAEGAIDAASILKPMLARGELQTIGATTLDEYRKHLEKDAALERRFQPIQVAEPSLPHTIEILKGLRDRYEAHHRVSITDEALVQAATLADRYISDRFLPDKAIDLIDEAGSRMRIRRMTAPPDLREFDEKIAGVRRDKESAIDSQDFEKAASLRDKEKQLLAAKAKREKEWKAGDMDVVAEVDGELIAEVLATATGIPVFKLTEEESSRLLRMEDELHKRVIGQKDAVKALSKAIRRTRAGLKDPKRPGGSFIFAGPSGVGKTELSKALAEFLFGDEDALISLDMSEFSEKHTVSRLFGSPPGYVGYEEGGQLTEKVRRKPFSVVLFDEVEKAHPDIFNSLLQILEDGRLTDSQGRVVDFKNTVIIMTTNLGTRDISKGFNLGFAASGDKKTNYERMKNKVSDELKQHFRPEFLNRVDDVVVFPQLTQDDILQIVDLMISKVDERLKDRDMGIELSQSAKELLAKKGYDPVLGARPLRRTIQREVEDTLSEKILFGELRPGHIVVVDTEGEGETATFTFRGEEKAALPDVPPIESAAGGSGPNLSKEA
>NZ_CP030771.1|WP_138966899.1|5508245_5509799_+|ATP-binding-protein
MDALLWLALATPAATADAIGLNEPRTAWQQLGGLAALAAAAAIWRRRPTLAFLLAAAPGEATAPSLFTVSYGMALAAFAFLLGRHGPRARPALLAFAAVAAAGTAKVVVRDVDPVVEWLVLMATLLFGAVFPWLAGRYLRQSRALTASALARADQLEREQRIVADRARLRERARIAQDMHDSLGHELSLIAVRAGALQLAADLPEHHRAAARDLRVAAADATDRLREIIGVLRDEGDEPAPLAPPGETVAQLVARAGESGLRVRYVAEGAEEPGPAERLAYRVVQEALTNAAKYAPGAPVTVAATRADARTTITVTNGPPREPGSPPGGGSGLADLHTRLAALGGDLDAGAHAGGFRVRAVIPADAGVAVAAPAPADTVPLPSGTLAHARRRTVLAFGAAAATGAVLIAGTFGWYAYTKTHSVLRPADFAALRVGAAQADVAAVLPERGVSDPPVDRAPGPPPPGADCRYYRSSGQLFTSSAHFRLCFENGKLVDKTVIPKPGASGGPGTGGDGGRR
>NZ_CP030771.1|WP_138961134.1|5509795_5510482_+|response-regulator
MIRVVLADDEAMIRAGVRAILTAGDGIEVVAEAADGREAIELAQAHRPDVALLDIRMPRLDGLAAGEEIVRTLPGTAVAMLTTFSEDAYVARALGGGATGFLLKSGDPHELIAGVRAVAGGAAFLSPKVARYVIDGLGGRRIGRESAARTRVAALTPREREVLGLVGAGLSNPEIAARLHLVEGTVKAYVSAVLDRLEVKNRVQAAIVAYEAGLVADDGARTAPGAPG
>NZ_CP030771.1|WP_138961135.1|5511826_5512660_+|hypothetical-protein
MGSLRNPIGPLPSSIYWRRRAVLLSVLGLLLLLVIWALASGGGGGKTGADGPSGNGPATSITPGPSGSGPAISEHPGGRDESEGSGGSGGSGGSGGSGGSGGGGDSGSGGGSGEDSGGAGSGSDDGAKGGGGSGSRLPAGSTLPNCAPGAVKLKLRSLRNEYEAGQKPKLELTAVNTGSKACKVDLGAKGAVLTITQSGSGDEIWSSDDCPAAGGTSLLFRVPGGGRVSHVVEWDLKASAPQCATPPAGTAKPDTYLVEAKSEALGSDRASFVLTAD
>NZ_CP030771.1|WP_138961136.1|5512742_5513867_-|DNA-integrity-scanning-protein-DisA
MAANDRAAVPGKPGGGSGADGLMRASLSAVAPGTALRDGLERILRGNTGGLIVLGSDKTVESMCTGGFVLDVEFTATRLRELCKLDGGIVLSSDLSKILRAGVQLVPDPTIPTEETGTRHRTADRVSKQVGFPVVSVSQSMRLVALYVDGQRRVLEDSAAILSRANQALATLERYKLRLDEVAGTLSALEIEDLVTVRDVTAVAQRLEMVRRIATEIAEYVVELGTDGRLLALQLDELIAGVEPERELVVRDYVPEPTAKRSRTVDEALAELDSLTHAELLELSTVARALGYTGSPETLDSAVSPRGFRLLAKVPRLPGAIIERLVEHFGGLQKLLAASVDDLQTVDGVGEARARSVREGLSRLAESSILERYV
>NZ_CP030771.1|WP_138961137.1|5513957_5515367_-|DNA-repair-protein-RadA
MAARTKTAKDRPSYRCTECGWQTAKWLGRCPECQAWGTVEEYGAPAVRTTTPGRVTTSALPIGQVDGRQATARSTGVPELDRVLGGGLVPGAVVLLAGEPGVGKSTLLLDVAAKAATDGHRTLYVTGEESASQVRLRADRIGALADDLYLAAETDLAAVLGHLDAVKPSLLILDSVQTVASPEIDGAPGGMAQVREVAGALIRASKERGMSTLLVGHVTKDGAIAGPRLLEHLVDVVLHFEGDRHARLRLVRGVKNRYGATDEVGCFELHDEGIVGLADPSGLFLTRRAEPVPGTCLTVTLEGRRPLVAEVQALTVDSQIPSPRRTTSGLETSRVSMMLAVLEQRGRISALGKRDIYSATVGGVKLSEPAADLAVALALASAASDTPLPKNLVAIGEVGLAGEVRRVTGVQRRLAEAHRLGFTHALVPADPGKVPAGMKVTEVADMGDALRVLPRSRRREAPREEEDRR
>NZ_CP030771.1|WP_138961138.1|5515640_5517353_+|hypothetical-protein
MMSSSPEVPTHTTGAHRAYAGPRSRVVPRPVPQAPAAPYEPFLDGLFTYCLSVLCDHDTATTALGDVLALAERRGARPDGDTRAWLYALARWMCLRVLAEARKGGRQGAHAAGSGKIPPAPPHTTEAPPADEAERARRRELAQLAWPEAAGTTPEQREALELAVRHQLAPKEVAAVLGLDLTAARELLASAACEVERTRAALAVVETGTCPIVARLTGDNQVLLGTALRRELVRHVDDCPRCRRTAERAGAGAWPGTAVTPAALPLIEAPRAALHHAMAHAPRAPRRNRGGPRFDRRGFPMDPKDHAARRERFRARAVTTTVVATVVAAPVLALWAAYRGAPLTGEGTDGRASSASEADDGGRDGSRGRDSYENAGNARTTPDPRFAAGPGGPGVSVEVISPGAPAAPGAGRIGVQARSNGGVTLITLTASGSSPVRWSASTGAPWLLLSHASGTLAPGDSFTIRVYVDDDREPPGHWSARVTIAPSGAVISIEGYGSSRPSHPRPRPTPTRPGPADPDPTPTPSGDGDPTPTPPDPDPTPTDPAPTDPAPSPSDPGSTPPPSDGGPGQG
>NZ_CP030771.1|WP_138966901.1|5517362_5518307_-|hypothetical-protein
MSAPPARGGADGKASKESKADRAAEGAKGEKTAKAGKKDKAGKAGRADKAVRKLRRAADGAVPADDEKGLDFPRAWVEFPDPADEEQIFRCDLTWLTSRWTCVFGSGCQGIQAGRADDGCCTLGAHFSDEDDEKRVATFVERLTPDIWQHHDVGRETGWVSQDEDGERQTRPYNGSCVFQNRPGFAGGAGCSLHILALKEGREPLETKPDVCWQLPVRRTYDWIERPDDTKVLQVSIGEYDRRGWGPGGHDLHWWCTSATSAHGAGDPVYVSYRPELIELMGKAGYDRLVELCEARLASQLPLLAPHPADPPRA
>NZ_CP030771.1|WP_138961139.1|5518444_5519377_+|Ppx/GppA-family-phosphatase
MRLGVLDVGSNTVHLLVVDAHPGARPLPAHSHKADLRLAQLLDPAGAIGPEGVDQLIATVRDALQAAEDKGVEDLLPFATSAVREATNADDVLARVRAETGVDLQVLTGEEEARLTFLAVRRWFGWSAGKLLVLDIGGGSLEIAYGMDEEPDAAVSLPLGAGRLTAAWLPEDPPEPGDVRALRRHVRAQIARTVGEFSRLGSPDHVVATSKTFKQLARLGGAARSTEGLYVQRELKRKSLEDWVPQLAAMTVGERSELPGVSEGRAGQLLAGALVAEGAMDLFGVESVEICPWALREGVILRRLDHLPAR
>NZ_CP030771.1|WP_138961140.1|5519962_5520787_+|TIM-barrel-protein
MVEPVVRIPDAKVALSTASVYPESTATAFEIAARLGYDGVEVMVWTDPVSQDIEALRRLSDYHQIPILAVHAPCLLITQRVWSTDPWVKLQRARAAAEKLDASTVVVHPPFRWQRGYARDFVQGIWRMAEETDVRFAVENMYPWRYRDREMLAYAPDWDVTKDDYRHFTIDLSHTATARTDALQMVDRMGDRLGHVHLADGRGSAKDEHLVPGRGTQPCAALLERLATSGFDGHVVIEVNTRRAMSSAEREADLAEALAFTRLHLASSAKVPRP
>NZ_CP030771.1|WP_138961141.1|5520783_5521416_+|TetR-family-transcriptional-regulator
MTASAAAPRRRGRPSRTQTERGPATRETILDAARDQFSAHGYEKTSVRAIAKAAGVDSALVHHYFGTKEQLFAAAVEVSFAPALQAPAAIQDGPLDAVGERLTRFVLGVWEDPATRTPLLAIVRSAVNNETAAAVFRRLVSTQLLSRIAGTLDLPDAELRAELAAAQLVGVAMLRYVIQVEPLASADLEELVARVAPVVQGHLTGFPGPA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_12

5519707-5519804

Orphan

Consensus_repeat	Method
GTCCGGCGTTTGAGGACGAGCGCGTCAGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_12

>merge|NZ_CP030771|12|5519707-5519804|CRISPRCasFinder
GTCCGGCGTTTGAGGACGAGCGCGTCAGCGTGATGAATGGCAACGGCGCCGCAGGGAAGATCCAGCCTGTCCGGCGTTTGAGGACAAGCGCGTCAGCG

>NZ_CP030771|12|11|5519707-5519804|CRISPRCasFinder
GTCCGGCGTTTGAGGACGAGCGCGTCAGCG	TGATGAATGGCAACGGCGCCGCAGGGAAGATCCAGCCT
GTCCGGCGTTTGAGGACAAGCGCGTCAGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138966899.1\|5508245_5509799_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|226951
NZ_CP030771.1\|WP_138966901.1\|5517362_5518307_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_171075826.1\|5523737_5524055_+\|SH3-domain-containing-protein	unknown	unknown	gnl\|CDD\|227324
NZ_CP030771.1\|WP_138961138.1\|5515640_5517353_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274357
NZ_CP030771.1\|WP_138961146.1\|5528603_5529341_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|272861
NZ_CP030771.1\|WP_138961134.1\|5509795_5510482_+\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP030771.1\|WP_138961132.1\|5505733_5506273_-\|SigE-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|132028
NZ_CP030771.1\|WP_138961136.1\|5512742_5513867_-\|DNA-integrity-scanning-protein-DisA	unknown	unknown	gnl\|CDD\|237395
NZ_CP030771.1\|WP_138961148.1\|5530374_5530992_-\|isochorismatase-family-protein	unknown	unknown	gnl\|CDD\|238496
NZ_CP030771.1\|WP_138961144.1\|5526566_5527073_+\|EamA/RhaT-family-transporter	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961140.1\|5519962_5520787_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138961137.1\|5513957_5515367_-\|DNA-repair-protein-RadA	unknown	unknown	gnl\|CDD\|236994
NZ_CP030771.1\|WP_138961143.1\|5524127_5526404_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|270916
NZ_CP030771.1\|WP_138961135.1\|5511826_5512660_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|164795
NZ_CP030771.1\|WP_138961142.1\|5521721_5523575_+\|dihydroxy-acid-dehydratase	unknown	unknown	gnl\|CDD\|237104
NZ_CP030771.1\|WP_138961133.1\|5506529_5507462_-\|A/G-specific-adenine-glycosylase	unknown	unknown	gnl\|CDD\|224115
NZ_CP030771.1\|WP_138961147.1\|5529442_5530270_+\|pyrroline-5-carboxylate-reductase	unknown	unknown	gnl\|CDD\|237008
NZ_CP030771.1\|WP_138961145.1\|5527332_5528181_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP030771.1\|WP_138961139.1\|5518444_5519377_+\|Ppx/GppA-family-phosphatase	unknown	unknown	gnl\|CDD\|223326
NZ_CP030771.1\|WP_138961141.1\|5520783_5521416_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380054

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138966899.1\|5508245_5509799_+\|ATP-binding-protein	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	6.14807e-25
NZ_CP030771.1\|WP_171075826.1\|5523737_5524055_+\|SH3-domain-containing-protein	gnl\|CDD\|227324	COG4991, COG4991, Uncharacterized protein with a bacterial SH3 domain homologue [Function unknown].	6.44412e-09
NZ_CP030771.1\|WP_138961138.1\|5515640_5517353_+\|hypothetical-protein	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	2.84917e-09
NZ_CP030771.1\|WP_138961146.1\|5528603_5529341_+\|ABC-transporter-permease	gnl\|CDD\|272861	TIGR00025, Mtu_efflux, ABC transporter efflux protein, DrrB family. The seed members for this model are a paralogous family of Mycobacterium tuberculosis. Nearly all proteins scoring above the noise cutoff are from high-GC Gram-positive organisms. The members of this paralogous family of efflux proteins are all found in operons with ATP-binding chain partners. They are related to a putative daunorubicin resistance efflux protein of Streptomyces peucetius. This model represents a branch of a larger superfamily that also includes NodJ, a part of the NodIJ pair of nodulation-triggering signal efflux proteins. The members of this branch may all act in antibiotic resistance.	1.07616e-24
NZ_CP030771.1\|WP_138961134.1\|5509795_5510482_+\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.90068e-69
NZ_CP030771.1\|WP_138961132.1\|5505733_5506273_-\|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.	4.60706e-58
NZ_CP030771.1\|WP_138961136.1\|5512742_5513867_-\|DNA-integrity-scanning-protein-DisA	gnl\|CDD\|237395	PRK13482, PRK13482, DNA integrity scanning protein DisA; Provisional.	0
NZ_CP030771.1\|WP_138961148.1\|5530374_5530992_-\|isochorismatase-family-protein	gnl\|CDD\|238496	cd01014, nicotinamidase_related, Nicotinamidase_ related amidohydrolases. Cysteine hydrolases of unknown function that share the catalytic triad with other amidohydrolases, like nicotinamidase, which converts nicotinamide to nicotinic acid and ammonia.	1.82236e-55
NZ_CP030771.1\|WP_138961140.1\|5519962_5520787_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	9.53999e-29
NZ_CP030771.1\|WP_138961137.1\|5513957_5515367_-\|DNA-repair-protein-RadA	gnl\|CDD\|236994	PRK11823, PRK11823, DNA repair protein RadA; Provisional.	0
NZ_CP030771.1\|WP_138961143.1\|5524127_5526404_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	4.39127e-82
NZ_CP030771.1\|WP_138961135.1\|5511826_5512660_+\|hypothetical-protein	gnl\|CDD\|164795	PHA00370, III, attachment protein.	2.60493e-06
NZ_CP030771.1\|WP_138961142.1\|5521721_5523575_+\|dihydroxy-acid-dehydratase	gnl\|CDD\|237104	PRK12448, PRK12448, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP030771.1\|WP_138961133.1\|5506529_5507462_-\|A/G-specific-adenine-glycosylase	gnl\|CDD\|224115	COG1194, MutY, A/G-specific DNA glycosylase [DNA replication, recombination, and repair].	1.80742e-79
NZ_CP030771.1\|WP_138961147.1\|5529442_5530270_+\|pyrroline-5-carboxylate-reductase	gnl\|CDD\|237008	PRK11880, PRK11880, pyrroline-5-carboxylate reductase; Reviewed.	5.86619e-104
NZ_CP030771.1\|WP_138961145.1\|5527332_5528181_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.23002e-84
NZ_CP030771.1\|WP_138961139.1\|5518444_5519377_+\|Ppx/GppA-family-phosphatase	gnl\|CDD\|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	3.26053e-81
NZ_CP030771.1\|WP_138961141.1\|5520783_5521416_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|380054	pfam17920, TetR_C_16, 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. This entry represents the C-terminal domain found in a number of different TetR transcription regulator proteins found in Actinobacteria. 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.	8.14013e-32

>NZ_CP030771.1|WP_138961139.1|5518444_5519377_+|Ppx/GppA-family-phosphatase
MRLGVLDVGSNTVHLLVVDAHPGARPLPAHSHKADLRLAQLLDPAGAIGPEGVDQLIATVRDALQAAEDKGVEDLLPFATSAVREATNADDVLARVRAETGVDLQVLTGEEEARLTFLAVRRWFGWSAGKLLVLDIGGGSLEIAYGMDEEPDAAVSLPLGAGRLTAAWLPEDPPEPGDVRALRRHVRAQIARTVGEFSRLGSPDHVVATSKTFKQLARLGGAARSTEGLYVQRELKRKSLEDWVPQLAAMTVGERSELPGVSEGRAGQLLAGALVAEGAMDLFGVESVEICPWALREGVILRRLDHLPAR
>NZ_CP030771.1|WP_138966901.1|5517362_5518307_-|hypothetical-protein
MSAPPARGGADGKASKESKADRAAEGAKGEKTAKAGKKDKAGKAGRADKAVRKLRRAADGAVPADDEKGLDFPRAWVEFPDPADEEQIFRCDLTWLTSRWTCVFGSGCQGIQAGRADDGCCTLGAHFSDEDDEKRVATFVERLTPDIWQHHDVGRETGWVSQDEDGERQTRPYNGSCVFQNRPGFAGGAGCSLHILALKEGREPLETKPDVCWQLPVRRTYDWIERPDDTKVLQVSIGEYDRRGWGPGGHDLHWWCTSATSAHGAGDPVYVSYRPELIELMGKAGYDRLVELCEARLASQLPLLAPHPADPPRA
>NZ_CP030771.1|WP_138961138.1|5515640_5517353_+|hypothetical-protein
MMSSSPEVPTHTTGAHRAYAGPRSRVVPRPVPQAPAAPYEPFLDGLFTYCLSVLCDHDTATTALGDVLALAERRGARPDGDTRAWLYALARWMCLRVLAEARKGGRQGAHAAGSGKIPPAPPHTTEAPPADEAERARRRELAQLAWPEAAGTTPEQREALELAVRHQLAPKEVAAVLGLDLTAARELLASAACEVERTRAALAVVETGTCPIVARLTGDNQVLLGTALRRELVRHVDDCPRCRRTAERAGAGAWPGTAVTPAALPLIEAPRAALHHAMAHAPRAPRRNRGGPRFDRRGFPMDPKDHAARRERFRARAVTTTVVATVVAAPVLALWAAYRGAPLTGEGTDGRASSASEADDGGRDGSRGRDSYENAGNARTTPDPRFAAGPGGPGVSVEVISPGAPAAPGAGRIGVQARSNGGVTLITLTASGSSPVRWSASTGAPWLLLSHASGTLAPGDSFTIRVYVDDDREPPGHWSARVTIAPSGAVISIEGYGSSRPSHPRPRPTPTRPGPADPDPTPTPSGDGDPTPTPPDPDPTPTDPAPTDPAPSPSDPGSTPPPSDGGPGQG
>NZ_CP030771.1|WP_138961137.1|5513957_5515367_-|DNA-repair-protein-RadA
MAARTKTAKDRPSYRCTECGWQTAKWLGRCPECQAWGTVEEYGAPAVRTTTPGRVTTSALPIGQVDGRQATARSTGVPELDRVLGGGLVPGAVVLLAGEPGVGKSTLLLDVAAKAATDGHRTLYVTGEESASQVRLRADRIGALADDLYLAAETDLAAVLGHLDAVKPSLLILDSVQTVASPEIDGAPGGMAQVREVAGALIRASKERGMSTLLVGHVTKDGAIAGPRLLEHLVDVVLHFEGDRHARLRLVRGVKNRYGATDEVGCFELHDEGIVGLADPSGLFLTRRAEPVPGTCLTVTLEGRRPLVAEVQALTVDSQIPSPRRTTSGLETSRVSMMLAVLEQRGRISALGKRDIYSATVGGVKLSEPAADLAVALALASAASDTPLPKNLVAIGEVGLAGEVRRVTGVQRRLAEAHRLGFTHALVPADPGKVPAGMKVTEVADMGDALRVLPRSRRREAPREEEDRR
>NZ_CP030771.1|WP_138961136.1|5512742_5513867_-|DNA-integrity-scanning-protein-DisA
MAANDRAAVPGKPGGGSGADGLMRASLSAVAPGTALRDGLERILRGNTGGLIVLGSDKTVESMCTGGFVLDVEFTATRLRELCKLDGGIVLSSDLSKILRAGVQLVPDPTIPTEETGTRHRTADRVSKQVGFPVVSVSQSMRLVALYVDGQRRVLEDSAAILSRANQALATLERYKLRLDEVAGTLSALEIEDLVTVRDVTAVAQRLEMVRRIATEIAEYVVELGTDGRLLALQLDELIAGVEPERELVVRDYVPEPTAKRSRTVDEALAELDSLTHAELLELSTVARALGYTGSPETLDSAVSPRGFRLLAKVPRLPGAIIERLVEHFGGLQKLLAASVDDLQTVDGVGEARARSVREGLSRLAESSILERYV
>NZ_CP030771.1|WP_138961135.1|5511826_5512660_+|hypothetical-protein
MGSLRNPIGPLPSSIYWRRRAVLLSVLGLLLLLVIWALASGGGGGKTGADGPSGNGPATSITPGPSGSGPAISEHPGGRDESEGSGGSGGSGGSGGSGGSGGGGDSGSGGGSGEDSGGAGSGSDDGAKGGGGSGSRLPAGSTLPNCAPGAVKLKLRSLRNEYEAGQKPKLELTAVNTGSKACKVDLGAKGAVLTITQSGSGDEIWSSDDCPAAGGTSLLFRVPGGGRVSHVVEWDLKASAPQCATPPAGTAKPDTYLVEAKSEALGSDRASFVLTAD
>NZ_CP030771.1|WP_138961134.1|5509795_5510482_+|response-regulator
MIRVVLADDEAMIRAGVRAILTAGDGIEVVAEAADGREAIELAQAHRPDVALLDIRMPRLDGLAAGEEIVRTLPGTAVAMLTTFSEDAYVARALGGGATGFLLKSGDPHELIAGVRAVAGGAAFLSPKVARYVIDGLGGRRIGRESAARTRVAALTPREREVLGLVGAGLSNPEIAARLHLVEGTVKAYVSAVLDRLEVKNRVQAAIVAYEAGLVADDGARTAPGAPG
>NZ_CP030771.1|WP_138966899.1|5508245_5509799_+|ATP-binding-protein
MDALLWLALATPAATADAIGLNEPRTAWQQLGGLAALAAAAAIWRRRPTLAFLLAAAPGEATAPSLFTVSYGMALAAFAFLLGRHGPRARPALLAFAAVAAAGTAKVVVRDVDPVVEWLVLMATLLFGAVFPWLAGRYLRQSRALTASALARADQLEREQRIVADRARLRERARIAQDMHDSLGHELSLIAVRAGALQLAADLPEHHRAAARDLRVAAADATDRLREIIGVLRDEGDEPAPLAPPGETVAQLVARAGESGLRVRYVAEGAEEPGPAERLAYRVVQEALTNAAKYAPGAPVTVAATRADARTTITVTNGPPREPGSPPGGGSGLADLHTRLAALGGDLDAGAHAGGFRVRAVIPADAGVAVAAPAPADTVPLPSGTLAHARRRTVLAFGAAAATGAVLIAGTFGWYAYTKTHSVLRPADFAALRVGAAQADVAAVLPERGVSDPPVDRAPGPPPPGADCRYYRSSGQLFTSSAHFRLCFENGKLVDKTVIPKPGASGGPGTGGDGGRR
>NZ_CP030771.1|WP_138961133.1|5506529_5507462_-|A/G-specific-adenine-glycosylase
MPTALAADRADSRAAEGPSSHGRLHSPVIAWFEAHARDLPWRRPDAGPWGVMVSEFMLQQTPVARVLPVYEQWVARWPRPADLAKEAPGEAVRAWGRLGYPRRALRLHGAAVAITERHGGDVPTQHAQLLALPGIGEYTAAAVASFAYGQRHAVLDTNVRRVFARAVTGVQYPPNATTAAERKLARALLPEDEATAARWAAASMELGALVCTAKNEDCGRCPIAAHCAWLTAGKPAHEGPARRGQTYAGTDRQVRGKLLAVLREAVTPVPQSALDRVWDEPVQRARALDGLVADGLVEPLPDGFYRLPLT
>NZ_CP030771.1|WP_138961132.1|5505733_5506273_-|SigE-family-RNA-polymerase-sigma-factor
MAHGEVLEFEEYVRTRQDALLRSARRLVPDPVDAQDLLQTALVRTYGRWDGIADKRLADAYLRRVMINTRTEWWRARKLEEVPTEQLPDASVDDSTEQHADRALLMDIMKVLAPKQRSVVVLRHWEQMSTEETAAALGMSAGTVKSTLHRALARLRQELESRDLDARVFEREERERCAA
>NZ_CP030771.1|WP_138961140.1|5519962_5520787_+|TIM-barrel-protein
MVEPVVRIPDAKVALSTASVYPESTATAFEIAARLGYDGVEVMVWTDPVSQDIEALRRLSDYHQIPILAVHAPCLLITQRVWSTDPWVKLQRARAAAEKLDASTVVVHPPFRWQRGYARDFVQGIWRMAEETDVRFAVENMYPWRYRDREMLAYAPDWDVTKDDYRHFTIDLSHTATARTDALQMVDRMGDRLGHVHLADGRGSAKDEHLVPGRGTQPCAALLERLATSGFDGHVVIEVNTRRAMSSAEREADLAEALAFTRLHLASSAKVPRP
>NZ_CP030771.1|WP_138961141.1|5520783_5521416_+|TetR-family-transcriptional-regulator
MTASAAAPRRRGRPSRTQTERGPATRETILDAARDQFSAHGYEKTSVRAIAKAAGVDSALVHHYFGTKEQLFAAAVEVSFAPALQAPAAIQDGPLDAVGERLTRFVLGVWEDPATRTPLLAIVRSAVNNETAAAVFRRLVSTQLLSRIAGTLDLPDAELRAELAAAQLVGVAMLRYVIQVEPLASADLEELVARVAPVVQGHLTGFPGPA
>NZ_CP030771.1|WP_138961142.1|5521721_5523575_+|dihydroxy-acid-dehydratase
MPELRSRTVTHGRNMAGARALMRASGVPGADIGRKPIIAVANSFTEFVPGHTHLAPVGRIVSEAVREAGGIPREFNTIAVDDGIAMGHGGMLYSLPSRDLIADSVEYMVEAHCADALICISNCDKITPGMLMAALRLNIPTVFVSGGPMEAGKATLVNGTVRKLDLIDAMVDASNENVSDEDILRIEENACPTCGSCSGMFTANSMNCLTEAIGLSLPGNGSVLATHTARRALYERAGATVVEITKRYYDGDDASVLPRNIATHAAFENAMALDIAMGGSTNTILHLLAAAQEAEVGYDLTDIDAVSRRVPCLAKVAPNVAPQGTYYMEDVHRAGGIPAILGELYRGGLLNEDVHTVHSPSIKQWLDAWDVRGGSVAPEALELWHAAPGCKRSAEAFSQSERWETLDTDAANGCIRDVAHAYSQDGGLAVLKGNLAVDGAVVKTAGVDESIWTFEGPAVVCESQEEAVEKILNKQVKEGDVVVIRYEGPKGGPGMQEMLYPTSFLKGRGLGKACALVTDGRFSGGTSGLSIGHASPEAASGGTIALVEDGDRIRIDIPGRSIELLVDDAELARRREALGGTYAPKSRERKVSAALRAYAAMATSADKGAVRDVSRLG
>NZ_CP030771.1|WP_171075826.1|5523737_5524055_+|SH3-domain-containing-protein
MSSEELTMPATADVADGAALTIEAATARRYAIVEDVNVRSGPGTAYDKVGRLSAGTFVTIGCQKPGETVTGPTGTSKIWDRIGSGRYVSDTYVRTGSNGYVAPRC
>NZ_CP030771.1|WP_138961143.1|5524127_5526404_-|PQQ-binding-like-beta-propeller-repeat-protein
MSLRSGDPEEIGGYPLESRLGSGGMGTVFLARTASGRPVALKLIHQQFAGDEEFRIRFRQEVAAARRVSGAFTAAVVDADPEAQQPWMATAYIEGPTLAQRIAQRGPIVGMELRTLAIGLAEALRDIHRADVVHRDLKPSNVVLSAEGPRVIDFGISRAADQQTLTMTGRVIGTPPFMSPEQLQTPRGVGPSSDVFSLGTLLVYAATGQGPFDADSPYMTAYQVVHEAPTLDDVPGALRTAVEPCLAKDPAVRPTIDELLVRLRDLPVDLGAAAGDGGSRTRDTDTQHHLSDTSGATGASSAAGTSSAPGAASASDSSGTSDGSGPAPARGLGGRLRRRWRPVLAAVLGVAVIAGCVALLRPGADGPGGDGPDDNGRNMAVVGSPLPHGFKAWRQTVPPGGAKLPDELRCVPRGDSAYCGGGGVIATRIRVADGHRMWTAHHPGVPMQNTYLVGVSGNTVLGYRLLPDDSGPGEVVALDAARGKELWSARFGSKSMAVTGRSDDAEVIGSTVVMLNAARTHVEGRAVRSGKVLWRTPVPAGAVCSPLTAGGQAHVMCAPATEVEATAIRHATVRGLDPASGTFGRAVALRGPLQVLGAYDGRLVLAKERVGEIGVVEYESVVHVDVARGKATTARLPKRYGGSPSLAAGTVYFTEQNGEVSAVDAVTGKLRWTRQAGVEGASGPVAGPGALYFSSASGRVAALAPRDGRRLWTADPKANGSAEVGTSPRVALAGRAAIVTGAGNLVYAFDTAKPPKSG
>NZ_CP030771.1|WP_138961144.1|5526566_5527073_+|EamA/RhaT-family-transporter
MSDERRTEQTEGTPAGPLPEPIRFFGTTWLEHTDGYAARRVGVAAGSLVAAAAGCLVLRFAYQGLEIADVGTFVNVLVVVMFAICSAIAFRRTWDGFSKRHDPQSVASMRSLMTIGFIGSLLAYFFRSLKEAPGERLHREEYETARDQYERRTKRRAGNPAKRKRRQK
>NZ_CP030771.1|WP_138961145.1|5527332_5528181_+|ATP-binding-cassette-domain-containing-protein
MMNIATPPRAPARATAPAAIHAHTLKAVRGHRTVLRDLTFTVPRGQITGLLGPSGCGKSTLMRAVVGTQAKVTGTLDVLDHPAGTPALRSRIGYVTQDPSVYEDLTVRQNLEYFAAVLTPGRGPAAARRREDVTRAIADVDLTSHADALAGNLSGGQRNRVSLAVALLGAPELLVLDEPTVGLDPVLRRDLWNLFHTLSDERGTTILVSSHVMDEAERCHRLLLMREGEILADDTPDALRERTGTGTVEEAFLHLVDKANATRHPDEPTAAQAHDTREPQLP
>NZ_CP030771.1|WP_138961146.1|5528603_5529341_+|ABC-transporter-permease
MNIHRTLATAARVLRQLRHDPRSIALLVLVPCVMLLLLRYVFDGSPRTFDSIGASLLGIFPLITMFLVTSIATLRERTSGTLERLLAMPLAKGDLIAGYALAFGTLAIIQSALATGLALWGLGLDVTGSAWLLLLVALLDALLGTALGLFVSAFAASEFQAVQFMPAVIFPQLLLCGLFTPRDKMQPVLEALSDALPMSYAVDGMNEVLRHPDITGTFVRDAVIVAACAVLVLALGAATLRRRTA
>NZ_CP030771.1|WP_138961147.1|5529442_5530270_+|pyrroline-5-carboxylate-reductase
MSQTRKPSQTVAVLGTGKIGEALLSGMIRSGWAPAELLVTTRRQERADELRTRYGVEALTNAEAAKRADTLILACKPQDMARLLDELAPHVAADRLVISAAAGITTSFIEERLTTGTPVIRVMPNTPVLVDEGMSVISGGTHATAGHLTHAENIFGAVGKTLRVPETQQDACTALSGSGPAYFYFLVEAMTDAGILLGLPRDKAHDLIVQAAIGAAVMLRDSGEHPVKLREAVTSPAGTTINAIRELENHGVRAALIAALEAARDRSRELASGSG
>NZ_CP030771.1|WP_138961148.1|5530374_5530992_-|isochorismatase-family-protein
MEIAENAALIVVDVQQGFEEVEYWGERNNPEADDNIAALIRAWQETGRPVVFVRHDSVKPDSPLRSGYAGNGFKEYVEERRGKGAGGELLVTKSVNSAFYGTPDLDAWLKEAGISQFVVTGIQTNMCAETTARMGGNLGYDVLFALDATYTFDLEGPFGWRLAAEEIARATAVSLHGGGFAEVVTTDKLIAAASGPAGTSSPSGV

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_13

5630379-5630492

Orphan

Consensus_repeat	Method
ACGGCGCCGCAGAGAACATCCAGCCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_13

>merge|NZ_CP030771|13|5630379-5630492|CRISPRCasFinder
ACGGCGCCGCAGAGAACATCCAGCCCGCACCGGCCACCCCAGCCCGTCCGGCGTTTGAGGACGAGCGCGTCAGCGCGATGAATGACCACGGCGCCGCAGGGAACATCCAGCCCG

>NZ_CP030771|13|12|5630379-5630492|CRISPRCasFinder
ACGGCGCCGCAGAGAACATCCAGCCCG	CACCGGCCACCCCAGCCCGTCCGGCGTTTGAGGACGAGCGCGTCAGCGCGATGAATGACC
ACGGCGCCGCAGGGAACATCCAGCCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138966927.1\|5626508_5627456_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223674
NZ_CP030771.1\|WP_138961214.1\|5629244_5630072_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224048
NZ_CP030771.1\|WP_138961218.1\|5640208_5640508_+\|WXG100-family-type-VII-secretion-target	unknown	unknown	gnl\|CDD\|377587
NZ_CP030771.1\|WP_138961206.1\|5620720_5621035_-\|AzlD-domain-containing-protein	unknown	unknown	gnl\|CDD\|377512
NZ_CP030771.1\|WP_138961207.1\|5621031_5621766_-\|AzlC-family-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224215
NZ_CP030771.1\|WP_138961211.1\|5624798_5626490_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173853
NZ_CP030771.1\|WP_016645643.1\|5630697_5630901_-\|cold-shock-protein	unknown	unknown	gnl\|CDD\|224197
NZ_CP030771.1\|WP_138961220.1\|5643781_5644102_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236323
NZ_CP030771.1\|WP_171076114.1\|5640620_5641133_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961209.1\|5622497_5623478_-\|SIS-domain-containing-protein	unknown	unknown	gnl\|CDD\|224651
NZ_CP030771.1\|WP_138961213.1\|5628300_5629248_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223521
NZ_CP030771.1\|WP_138961219.1\|5642573_5643785_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961212.1\|5627452_5628301_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224094
NZ_CP030771.1\|WP_138961215.1\|5632255_5633263_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366286
NZ_CP030771.1\|WP_138961216.1\|5633408_5635094_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP030771.1\|WP_138966929.1\|5631382_5632237_+\|menaquinone-biosynthesis-protein	unknown	unknown	gnl\|CDD\|270352
NZ_CP030771.1\|WP_138961221.1\|5644353_5645016_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961208.1\|5621812_5622472_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP030771.1\|WP_138961210.1\|5623569_5624802_+\|acyl-coenzyme-A--6-aminopenicillanic-acid-acyltransferase-form	unknown	unknown	gnl\|CDD\|367486
NZ_CP030771.1\|WP_138961217.1\|5635254_5639844_-\|cell-division-protein-FtsK	unknown	unknown	gnl\|CDD\|274860

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138966927.1\|5626508_5627456_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.10709e-106
NZ_CP030771.1\|WP_138961214.1\|5629244_5630072_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	2.44377e-98
NZ_CP030771.1\|WP_138961218.1\|5640208_5640508_+\|WXG100-family-type-VII-secretion-target	gnl\|CDD\|377587	pfam06013, WXG100, Proteins of 100 residues with WXG. ESAT-6 is a small protein appears to be of fundamental importance in virulence and protective immunity in Mycobacterium tuberculosis. homologs have been detected in other Gram-positive bacterial species. It may represent a novel secretion system potentially driven by the pfam01580 domains in the YukA-like proteins.	1.99997e-13
NZ_CP030771.1\|WP_138961206.1\|5620720_5621035_-\|AzlD-domain-containing-protein	gnl\|CDD\|377512	pfam05437, AzlD, Branched-chain amino acid transport protein (AzlD). This family consists of a number of bacterial and archaeal branched-chain amino acid transport proteins. AzlD is known to be involved in conferring resistance to 4-azaleucine although its exact role is uncertain.	6.69822e-08
NZ_CP030771.1\|WP_138961207.1\|5621031_5621766_-\|AzlC-family-ABC-transporter-permease	gnl\|CDD\|224215	COG1296, AzlC, Predicted branched-chain amino acid permease (azaleucine resistance) [Amino acid transport and metabolism].	2.58463e-30
NZ_CP030771.1\|WP_138961211.1\|5624798_5626490_+\|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.	4.14354e-91
NZ_CP030771.1\|WP_016645643.1\|5630697_5630901_-\|cold-shock-protein	gnl\|CDD\|224197	COG1278, CspC, Cold shock proteins [Transcription].	5.45949e-36
NZ_CP030771.1\|WP_138961220.1\|5643781_5644102_-\|hypothetical-protein	gnl\|CDD\|236323	PRK08651, PRK08651, succinyl-diaminopimelate desuccinylase; Reviewed.	0.000990327
NZ_CP030771.1\|WP_138961209.1\|5622497_5623478_-\|SIS-domain-containing-protein	gnl\|CDD\|224651	COG1737, RpiR, Transcriptional regulators [Transcription].	1.18664e-36
NZ_CP030771.1\|WP_138961213.1\|5628300_5629248_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	8.04715e-133
NZ_CP030771.1\|WP_138961212.1\|5627452_5628301_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	5.24619e-69
NZ_CP030771.1\|WP_138961215.1\|5632255_5633263_-\|hypothetical-protein	gnl\|CDD\|366286	pfam00756, Esterase, Putative esterase. This family contains Esterase D. However it is not clear if all members of the family have the same function. This family is related to the pfam00135 family.	3.85024e-10
NZ_CP030771.1\|WP_138961216.1\|5633408_5635094_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	4.79654e-85
NZ_CP030771.1\|WP_138966929.1\|5631382_5632237_+\|menaquinone-biosynthesis-protein	gnl\|CDD\|270352	cd13634, PBP2_Sco4506, The conserved hypothetical protein SCO4506 exhibits the type 2 periplasmic-binidng protein fold. This group includes the SCO4506 protein from Streptomyces coelicolor and related hypothetical proteins. SCO4506 is an ortholog of Ttha1568 (MqnD) from Thermus thermophilies HB8. MqnD is an enzyme within an alternative menaquinone biosynthetic pathway that catalyzes the conversion of cyclic de-hypoxanthine futalosine to 1,4-dihydroxy-6-naphthoate. Menaquinone (MK; vitamin K) is an essential lipid-soluble carrier that shuttles electrons between membrane-bound protein complexes in the electron transport chain. SCO4506 has significant structural homology with the members of type 2 periplasmic-binding fold protein superfamily. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.93184e-111
NZ_CP030771.1\|WP_138961208.1\|5621812_5622472_+\|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.	1.00076e-14
NZ_CP030771.1\|WP_138961210.1\|5623569_5624802_+\|acyl-coenzyme-A--6-aminopenicillanic-acid-acyltransferase-form	gnl\|CDD\|367486	pfam03417, AAT, Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase.	1.22737e-10
NZ_CP030771.1\|WP_138961217.1\|5635254_5639844_-\|cell-division-protein-FtsK	gnl\|CDD\|274860	TIGR03928, T7_EssCb_Firm, type VII secretion protein EssC, C-terminal domain. This model describes the C-terminal domain, or longer subunit, of the Firmicutes type VII secretion protein EssC. This protein (homologous to EccC in Actinobacteria) and the WXG100 target proteins are the only homologous parts of type VII secretion between Firmicutes and Actinobacteria. [Protein fate, Protein and peptide secretion and trafficking].	1.17927e-133

>NZ_CP030771.1|WP_138961214.1|5629244_5630072_+|ATP-binding-cassette-domain-containing-protein
MTKTALLQATGLSKTYPLPGGGSHRAAHDVGFAVPEGGSLGIVGESGSGKTTVARMLVGLVPPDRGEITVAGRRREPRTPRTSRARLARAREIQMVFQDPYVSLDPRLTATQCLRTALRLHGKDERGGAAARDLLDRVGLGAREADARPRDLSGGQRQRLAIARALAVDPRVLVLDEAVAALDVSIQAQILQLLREIREETGVALVFVSHDLAVVRHVTDAVLVMRRGEVVEQGPTGRVLADPEHAYTRLLLASVPGENWDPAAVSRTREALPAR
>NZ_CP030771.1|WP_138961213.1|5628300_5629248_+|ATP-binding-cassette-domain-containing-protein
MLLDIDDVTVTVPGAARPLLDSVSLRVAEGEVVALVGESGSGKSTTARTALGLLPDGAGVSGSVRFDGTEVLTLTGERLRAHRAGSVALVHQDPRAALNPVRRVGDFLTERGATRAEAVALLASVGLPDPERRVRQRPHELSGGMLQRVVIAGALAARPRLLLADEATSALDVTTQADILALLRTLRAEHGLGLLFITHDLHLAAAYSDRVYVMYAGRVVEERTAKALFTTPSHPYTRGLLSCSPTLDALEAPLRPIPGRPPSLADVFEGCAFVERCGQARPECGTWDPEPVPLPDGGVSACLAAGTPVETEVKP
>NZ_CP030771.1|WP_138961212.1|5627452_5628301_+|ABC-transporter-permease-subunit
MTLTLGATNAVKAAGPRRPVGVLIAGTLLGLVVLAAALAPLLAPYAPDTIDLSSSLVGTGREHLLGTDSSGQDLLSRALYGARTSLVAPLLLLAVAGVLGVTLGVLAAWRGGWVDTLVSRLTDVMYAFPGLLFTVLIIAVFGTGTTTSVLALGLAFTPTIAKYTRSLALSEARKPYVDAYRVQGMGGARICARHLIPNLGRSVLGYLVVLFGEALMSLATLSYLGFGAQPPSCDWGLMVQEGQAAIVQGAMLPALVPGTAIALVVVCFNVVGVWAADRLGRQ
>NZ_CP030771.1|WP_138966927.1|5626508_5627456_+|ABC-transporter-permease-subunit
MAVRLVRRLAGVLATLLAASFVIFAAVYAAPGDPAVFLAGGRDKLTPERLAQVRAEYHLDEPLAAQYGRWLWDCLHLDLGRSFKYSDQVSDLVAARFPTTLQLVLYATVLFVVLGVGAGILAAVKRSTWVDSAVVGVTTLAASVPSFVAAIALVSFFGVRLGWFPVTGSGEGFLGTVHHLTLPALSLALGALALVSRVTRQAMVDAAASDHVAAARASGVPEREIVRRHVLRNALGPIVTMCGLVMAGMLAGTVVVETAFGLSGIGSLLVGAINTHDFPVAQAVLLLMVTGYIVVTTAVDAVHPLLDPRVKEVRS
>NZ_CP030771.1|WP_138961211.1|5624798_5626490_+|ABC-transporter-substrate-binding-protein
MTHPPTRPASPTGPAQAAPRRAARAAAGLLAASLLAAGCAGADTNALGGAPADAAKLTLRATTPPAQGRLDRADWLLEDEPDSLDLDRQGGSAGRVVLTNICERLYQLQPDMSVEPFLAEKARTPDDRTLVLTVRDGVTFHDGSELTAADVLWSLKRHAAKDMEQSDEFGNVSSMRRTGPRELTIRFKEPDALFTKALAGDAGIVWNPRRVTAAGKEFGTPGQADACSGPYRLKEWKSGDSLTIEAYADYWGTKPLTRRVVFRWASDSALVNALRTGAADGTYAESPNTAAALRRAKNLRQYYGPSTASLVLIPTARGGLKDPAIRRALSLSLDRKGIANSGYGGLVQPWAAPVGAGAWGYERPRFAAAQKKLGAAAPATPTADDLAEAKKLVKEAGAPDDPVVIGTDSSQGRTVVANATRAALQRIGVRAQIKTVPPAQFEEFYSDPQARDGIDVLVGDWYISKADPMGFYDNGLSDSSNNWVGFKDPAYDRLVHKALATLDDTERARLTTEAQRRFVDAAVWIPVAQVPTALVLSDRLTGPPSSQSYLYYPWAARLGARKG
>NZ_CP030771.1|WP_138961210.1|5623569_5624802_+|acyl-coenzyme-A--6-aminopenicillanic-acid-acyltransferase-form
MAPRTTSDRSARVLPVVEISGTPTERGRQYGEAVRPQLHAALGYYAAAFGQSAGLTWDQVTARAARWLKPVREYAPHLEEEMAGIAEGAGVDLLDVLALNARGEVIYDRSFKRMAAPEGAEGAATEAAADASTAADASVEAADGCTSFAAYGPASGDGHVYAGQNWDWRAGVADTVVMLRVVQPPRPTLIMQVEAGQIGRQGANSAGIALNANGLGGRFSDAVGLPQTVVRRSVLDQHAVTDAVDVLCRTRAHIASNALLTCREGFAIDLETTPAGHGWMYPKDGLLVHGNHYQAGVPAALAPGYRPLSPDSLVRVPRAEEGLAALRGATGPDESIKMIKQAMSDHLGHPESLCTHPDPRRPELRRWATLVSSCVDLTTGDYRVTAGTPCDRDYQHLPWNLYDGPFGDPR
>NZ_CP030771.1|WP_138961209.1|5622497_5623478_-|SIS-domain-containing-protein
MKISEPPEGGAADGPDRAAGEADGPAGGPTDGPDDAGGAARLRTAVRGQWETLSASERAVAQYLASVPAESLLFASAQELGSASGTSNATVVRALQRLGYAGLPALKRDLATDFTAAVAPEVRLAKRIAHVGRDLGGIWDEVFDEAQERIEHARRLTPDDALRTAVGVLADAGEIHAYGVAASELAARHLALTLGRVGRRARYVGATGFALADHLLALRQGDAVVIFQPGRDLAELSVLIERARAVGARVLLVTDELAERYGGRVDAVLTAPHTPTGITTEALTALVVADVLLLALTTLDEARAVDTSHQLTALREQLLSPRPRKG
>NZ_CP030771.1|WP_138961208.1|5621812_5622472_+|helix-turn-helix-domain-containing-protein
MDWYAERSGVVTVRTDHNTEGAGGAGGVEGGAEAPRAPRAPREWVAEALRRERARAGLSLSELAKRAGIAKSTLSQLEAATGNPGIETVWALAVALGVPFSALMESPAPAVTVIRAGEGPTMHAERSSYAGTLLSRGPSGLRRDIYHGAMEPGPVRESDPHNPGTVEHLVVSTGRLLAGPRDEPVELLPGDYMAYRGDVPHAYEALVPGTTFVLVMQHV
>NZ_CP030771.1|WP_138961207.1|5621031_5621766_-|AzlC-family-ABC-transporter-permease
MRSTHRTDDPTERTAGFVRFSDLPTDVLRDIALVLLADLVVGVSFGAIAVAGGLPVWVPVTMSLLVYAGSAQFSAVAVLTSGGGAAAAAATGLLLNTRTAAFSLAVADSLGRSWAARLVGAHLVTDETAAFVLAQPDARRRRAAFWISGIGLFVAWNTSVLAGALAGSALGDTARFGLDAAFPAVLVALVLPVLRDAGGGARRAAAIGAVLAVAAAPVLPAGLPVLLALLGLLATGRRPAGGAA
>NZ_CP030771.1|WP_138961206.1|5620720_5621035_-|AzlD-domain-containing-protein
MNAQLVCVLALAAGTYVFRLAGPLLHGRVELPARVQELLAVAATVILVALLATGAFTEGHAFAGWSRPAGVLVGAALAWKRAPFVMVVLGAAGATALLRLAGLS
>NZ_CP030771.1|WP_016645643.1|5630697_5630901_-|cold-shock-protein
MATGTVKWFNAEKGFGFIAQEGGGPDVFVHYSAINASGFRSLEENQAVTFDVTQGPKGPQAENVTPA
>NZ_CP030771.1|WP_138966929.1|5631382_5632237_+|menaquinone-biosynthesis-protein
MPSSRRTARPRVGHIQFLNCMPLYWGLARTGTLLDFELTKDTPEKLSEQLVRGDLDVGPVTLVEFLRNADDLVAFPDLAVGCDGPVMSCVIVSQVPLDRLDGARVALGSTSRTSVRLAQLLLAERHGVRPEYYTCPPDLGLMMQEADAAVLIGDAALRANLIDAPKLGLEVHDLGQMWKDWTGLPFVFAVWAARRDYLAREPEVVREVHKAFLASRDLSLDEVAKVAEQASRWESFDAGVLERYFTTLDFRFGGPQLEGVTEFARRVGPTTGFPGDVKVELLRP
>NZ_CP030771.1|WP_138961215.1|5632255_5633263_-|hypothetical-protein
MNIRRTTVALTAALAATAALLTGCSSDGDEPMSFDSASAPAPAQGHGSEHAGIRLPTGPRASFTTASTLDDGTKIGVTTLHGKKSGFTGKVWVWAPKQYFDPKYSHSGFPVLIALPGGPGYPNNYWMGTDLKLESSIAKWSREGKSQPFIVVMPVLNPDATFYYDGSDIPGQPKMGTWMTEDVPDFVKANFRTFTSRDGWGFMGSSSGGFVGLKSVLKHPEKFRAVIASGPDTVPDSPLWRGHEPQRLANDPGRLAERLIRRGGPEVDIAFQVGTAESGQPNLRAFMKKYGKGPVRTRLNVIQGGTHSARSYVPAMDDGPIQWISKKMKGPVPGS
>NZ_CP030771.1|WP_138961216.1|5633408_5635094_+|protein-kinase
MHPLEPDEPTAVGPYRLLGRLGSGGMGRVYVGRSAGGRTVAVKVVHPHFALDEEFRARFRREVEAARRVGGQWTAPVLDADPEAALPWVATGYAAGPSLTEAVRDAGPLPEHSARVLGAGLAEALAHVHALGLVHRDVKPSNVLLTLDGPRLIDFGIARATDGTASLTSTGVSIGSPGYMAPEQILGKAATGAADVFSLGASLVYAATGEPPFAGDTSAALLYKVVHEEPDLGALGGELRDLAAACLAKDAAARPAPAEVARRLAPEGAAPLVAAGWLPGPLVERVSRSAVRLLDLEAKGDGAGGAAASGPVSFAGPAVGVFGPPDASYGAGGPGAAVPPTPLPRGGPADARPSPVPPPPAAAPPGKVSLSVAATAAPGTPDGRGRRVSCTVALAVAGALAAVLVGSAFLFDVLPGSGAGGDGDGSAGKRPPAATGGASDSDGLVPKRYLGKWRGKASAQDGLVALGTFDVTISQVTKAGERVGTVTQTDLIGGTCVDVLTLTSATEKRLALKAVGATSNGGGCSQAAHTVWLRPVGSELQYTSEDPKAGDPEARLRRVRG
>NZ_CP030771.1|WP_138961217.1|5635254_5639844_-|cell-division-protein-FtsK
MRLTLTVVDPIGGGSADVVLDADPDSSVRDIAAELARTAGRSGAQVIPLGPHQPTPDGAPVLYVDGYAVDPGATVVTSPLREGAVVSLHDPAGCVPGEPTGLVELRVVGGPAAGAVHRLGIGRYDIGSGPAAYVRVDDPELAARALTLSVATDGTCRLVVRGGEEGGGEVTLDGAKFTGAEDGAWPLGSQLAAGNTLFELVRYAPPDAALKWSEDGAGLDYNRPPRLRPPERQTTFRLPSPPRDFEARPLPWLMALFPLVGAVIAAMIFNRWYYLIIAGLSPIMLFGNYFLDKKHGRKSHAKQVKEYKETKERIEKDAQDALVAERLDRRHAAPDPAAVLTLATGPRTRLWERRRTDADHLLLRFGTGTLPSDVVLDDPEQDEHKRQVTWTIEDAPVALGLKQLGVIGLAGPGDSAAALGRWAVAQTAALHSPMDVQFYVLTENSAWESWDWLRWLPHARPGGGQDVNVLIGTDAETVGARVGELTQVLDAREKVKQETRGQTGGFTDPDIVVVWDGSRRLRSLPGVVRILRDGPAVGIYALCLDTEQRFLPGECQAFVVAEPRARELADPAAGAAPGAGGIPPRPATAPAGGGFPSFHAWHTADAEAGRADTADELRLRVEQTGARRLLGVRPDFVSPAWCLRLARAVSPLRDISGETEDSALPGASRLLDVLQLEPPSREAITARWQSGGQSTTAVIGESYDGPFGIDLRKDGPHGLIAGTTGSGKSELLQTIVAALAVANTPENMTFVLVDYKGGSAFKDCVQLPHTVGMVTDLDAHLVERALESLGAELKRREHILADADAKDIEDYQDLVRRDPTRAPVPRLLIVIDEFASMVRDLPDFVTGLVNIAQRGRSLGIHLLLATQRPSGVVSPEIRANTNLRIALRVTDGGESSDVIDAPDAGHISKNTPGRAYVRLGHASLVPFQSGRVGGRRPGAADPQALAPWADELTWPGLGRATAARPRARAREDEEITDLKVLVDAIREANTALAVPAQHSPWLPALGEMLLLDAIVSPPAPAGALPPAPYGVEDLPADQARRPVAVDFATFGHLMIGGAPRSGRSQVLRTIAGSLARTHSCADVHLYGIDCGNGALNALTRLPHCGAVVSRNQTERVVRLVNRLKGELGRRQDLLAEKGYADIGEQRSGAAADERLPHLVVLLDRWEGWLPTLGEIDHGSLTDEVTALLREGASVGIHLVVTGDRQLLVGRVSSLTEDKYGLRLADRSDFSLLGIPSRKVPEEIPPGRAFRNESGTETQFALLSEDATGQGQAAALAAIGEAAAVRDADVPRRLRPFRVDTLPGRISFDEAWELRDPEASRSKLWALIGVGGDELMGHGPDLAEGVPAFVVAGPAKSGRSTVLMNAARSFLAQGVRLVVAAPRQSPLRGLDGTEGVLKVFTGDDIDEDDLEEAIDSATPRSPIAVLVDDGEILEDCDAASQFKRIIQRGADEGLALVLAGDEEDVCSGFSGWQVDAKKGRRGILLSPQDSSSGDLIGVRVSRSMVGGPVTPGKGLLHLGTGEPATVTTPF
>NZ_CP030771.1|WP_138961218.1|5640208_5640508_+|WXG100-family-type-VII-secretion-target
MSKDLDVTYQDMRDAAKHVVKEKDKLKEKLDGLRKYIANLVETGYVTKSSSKAFDENFDEFVRGAKDMLDGLDGMGDYLTTAADKFEQIDDELGKAARG
>NZ_CP030771.1|WP_171076114.1|5640620_5641133_-|hypothetical-protein
MLVPRDWFRIDLTLDRWRPQLKTFADRQAARRGMSAEAARGLWATLRNTAESGAAQGAIELFLRSEISDTGATPATLLVSLLPMSGALYVTPQELARSVTEHRGAATKVSVTRLPAGETVRVTTATTLDLYVNMPGKAGYLLLAFSVPLSGVESSLGGLCEAIAASLRWV
>NZ_CP030771.1|WP_138961219.1|5642573_5643785_-|hypothetical-protein
MTRPTDWEPLHDGDPVPGDPYEVARLGKELRNMADEIDKQARNIKALSSVESWDSDAGRAFHEIADGTSGRLKRSFERYDEAAKALGTKVVEGDTESKEYASELYRAQKVADKALEKYRAARSDQQTAVGDLDKYKGTVPSKDDIGDRTRLEKQRDEAMSVIRDCHGDIARAKSIRDDAASAAAKHIKNIIHHDGVRDPGGFMNWLADWADRFSNLSAIFAILAVICTFVPPLQVLAPVFAALSVVCSAAALAGHAYDMFKRGGKLNLLKLGLDVLGVMPGLGALKGFGALKGLKGLAKLRGVRFSGLGALKGVGFKFNNGIAVNLTNKILTKAKQMPIAGEKITAGIKTAGFGSALYKIFTGKDGARTGDPGDPVKPANLPRPSPRPAPTPSPTPFRTAMAQ
>NZ_CP030771.1|WP_138961220.1|5643781_5644102_-|hypothetical-protein
MSDRTRADLGMIRDCSDALFRIHREFKENSNPADEYGDALGSKKLRDVFDDFSGTWKKTRKKLMADIEKLAKFTDSAADTYDKVDHELAEALRNARKEAKEAKGKK
>NZ_CP030771.1|WP_138961221.1|5644353_5645016_-|hypothetical-protein
MTSAPQPTGEDIAPVLLPPLTFVVPDGFHDVPVDASADERPESAAAFVRGLYPGGDAELWGSAAPYYERVTTLLSTAGLLYSGLGIFGLGEEGVAHCSLSVAVCASRHDDTETAAQGMLAVLSGDPLNDARWLDLPCGPAISCVSMRELSVAAEQTTASEEQPKIITGQIQVYLPFPTGPYMAVFTLSTASMQCWGEFCDMLTAILQTASFTDPDAPDHA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_14

5799385-5799470

Orphan

Consensus_repeat	Method
CCCTCTTGTTTCGTCGGCGGCTTTCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_14

>merge|NZ_CP030771|14|5799385-5799470|CRISPRCasFinder
CCCTCTTGTTTCGTCGGCGGCTTTCCGCCGGTGGACCGGGAGCTCCCTCCCTGCGTGCGCCCTCTTGTTTCGTCGGCGGCTTTCCG

>NZ_CP030771|14|13|5799385-5799470|CRISPRCasFinder
CCCTCTTGTTTCGTCGGCGGCTTTCCG	CCGGTGGACCGGGAGCTCCCTCCCTGCGTGCG
CCCTCTTGTTTCGTCGGCGGCTTTCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138961332.1\|5797187_5797556_+\|holo-ACP-synthase	unknown	unknown	gnl\|CDD\|234610
NZ_CP030771.1\|WP_138961338.1\|5802962_5803511_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961341.1\|5805961_5806216_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961333.1\|5797668_5799156_+\|NAD(P)H-hydrate-dehydratase	unknown	unknown	gnl\|CDD\|238576
NZ_CP030771.1\|WP_138961339.1\|5803613_5804270_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	unknown	unknown	gnl\|CDD\|274750
NZ_CP030771.1\|WP_138961326.1\|5791142_5792369_+\|DUF2029-domain-containing-protein	unknown	unknown	gnl\|CDD\|378217
NZ_CP030771.1\|WP_138961327.1\|5792579_5793023_+\|50S-ribosomal-protein-L13	unknown	unknown	gnl\|CDD\|181703
NZ_CP030771.1\|WP_138961342.1\|5806233_5807502_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|380115
NZ_CP030771.1\|WP_138961343.1\|5807529_5808471_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|366688
NZ_CP030771.1\|WP_138961334.1\|5799540_5800698_+\|alanine-racemase	unknown	unknown	gnl\|CDD\|143481
NZ_CP030771.1\|WP_138966959.1\|5804305_5804857_+\|ribosomal-protein-S18-alanine-N-acetyltransferase	unknown	unknown	gnl\|CDD\|273701
NZ_CP030771.1\|WP_138961330.1\|5795064_5796015_-\|DUF389-domain-containing-protein	unknown	unknown	gnl\|CDD\|129372
NZ_CP030771.1\|WP_138961340.1\|5804849_5805965_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD	unknown	unknown	gnl\|CDD\|236585
NZ_CP030771.1\|WP_138961336.1\|5801929_5802445_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE	unknown	unknown	gnl\|CDD\|376771
NZ_CP030771.1\|WP_138961331.1\|5796070_5797069_-\|type-I-pantothenate-kinase	unknown	unknown	gnl\|CDD\|235466
NZ_CP030771.1\|WP_138961325.1\|5789343_5790198_+\|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl\|CDD\|234577
NZ_CP030771.1\|WP_138961335.1\|5800711_5801911_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|366166
NZ_CP030771.1\|WP_171075833.1\|5790219_5791068_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961329.1\|5793709_5795068_+\|phosphoglucosamine-mutase	unknown	unknown	gnl\|CDD\|237672
NZ_CP030771.1\|WP_138961328.1\|5793065_5793581_+\|30S-ribosomal-protein-S9	unknown	unknown	gnl\|CDD\|178888

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138961332.1\|5797187_5797556_+\|holo-ACP-synthase	gnl\|CDD\|234610	PRK00070, acpS, 4'-phosphopantetheinyl transferase; Provisional.	3.37829e-48
NZ_CP030771.1\|WP_138961333.1\|5797668_5799156_+\|NAD(P)H-hydrate-dehydratase	gnl\|CDD\|238576	cd01171, YXKO-related, B.subtilis YXKO protein of unknown function and related proteins. Based on the conservation of the ATP binding site, the substrate binding site and the Mg2+binding site and structural homology this group is a member of the ribokinase-like superfamily.	5.62178e-62
NZ_CP030771.1\|WP_138961339.1\|5803613_5804270_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	gnl\|CDD\|274750	TIGR03725, T6A_YeaZ, tRNA threonylcarbamoyl adenosine modification protein YeaZ. This family describes a protein family, YeaZ, now associated with the threonylcarbamoyl adenosine (t6A) tRNA modification. Members of this family may occur as fusions with ygjD (previously gcp) or the ribosomal protein N-acetyltransferase rimI, and is frequently encoded next to rimI. [Protein synthesis, tRNA and rRNA base modification].	5.34907e-61
NZ_CP030771.1\|WP_138961326.1\|5791142_5792369_+\|DUF2029-domain-containing-protein	gnl\|CDD\|378217	pfam09594, GT87, Glycosyltransferase family 87. The enzymes in this family are glycosyltransferases. PimE is involved in phosphatidylinositol mannoside (PIM) synthesis, a major class of glycolipids in all mycobacteria. PimE is a polyprenol-phosphate-mannose-dependent mannosyltransferase that transfers the fifth mannose of PIM. The family also includes alpha(1-->3) arabinofuranosyltransferase, invloved in the synthesis of of mycobacterial arabinogalactan.	5.16857e-09
NZ_CP030771.1\|WP_138961327.1\|5792579_5793023_+\|50S-ribosomal-protein-L13	gnl\|CDD\|181703	PRK09216, rplM, 50S ribosomal protein L13; Reviewed.	9.17549e-101
NZ_CP030771.1\|WP_138961342.1\|5806233_5807502_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|380115	pfam18096, Thump_like, THUMP domain-like. This is a domain of unknown function found in bacteria.	2.09863e-18
NZ_CP030771.1\|WP_138961343.1\|5807529_5808471_+\|polysaccharide-deacetylase-family-protein	gnl\|CDD\|366688	pfam01522, Polysacc_deac_1, Polysaccharide deacetylase. This domain is found in polysaccharide deacetylase. This family of polysaccharide deacetylases includes NodB (nodulation protein B from Rhizobium) which is a chitooligosaccharide deacetylase. It also includes chitin deacetylase from yeast, and endoxylanases which hydrolyzes glucosidic bonds in xylan.	3.10174e-34
NZ_CP030771.1\|WP_138961334.1\|5799540_5800698_+\|alanine-racemase	gnl\|CDD\|143481	cd00430, PLPDE_III_AR, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Alanine Racemase. This family includes predominantly bacterial alanine racemases (AR), some serine racemases (SerRac), and putative bifunctional enzymes containing N-terminal UDP-N-acetylmuramoyl-tripeptide:D-alanyl-D-alanine ligase (murF) and C-terminal AR domains. These proteins are fold type III PLP-dependent enzymes that play essential roles in peptidoglycan biosynthesis. AR catalyzes the interconversion between L- and D-alanine, which is an essential component of the peptidoglycan layer of bacterial cell walls. SerRac converts L-serine into its D-enantiomer (D-serine) for peptidoglycan synthesis. murF catalyzes the addition of D-Ala-D-Ala to UDPMurNAc-tripeptide, the final step in the synthesis of the cytoplasmic precursor of bacterial cell wall peptidoglycan. Members of this family contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. AR and other members of this family require dimer formation and the presence of the PLP cofactor for catalytic activity. Fungal ARs and eukaryotic serine racemases, which are fold types I and II PLP-dependent enzymes respectively, are excluded from this family.	5.71007e-159
NZ_CP030771.1\|WP_138966959.1\|5804305_5804857_+\|ribosomal-protein-S18-alanine-N-acetyltransferase	gnl\|CDD\|273701	TIGR01575, rimI, ribosomal-protein-alanine acetyltransferase. Members of this model belong to the GCN5-related N-acetyltransferase (GNAT) superfamily. This model covers prokarotes and the archaea. The seed contains a characterized accession for Gram negative E. coli. An untraceable characterized accession (PIR\|S66013) for Gram positive B. subtilis scores well (205.0) in the full alignment. Characterized members are lacking in the archaea. Noise cutoff (72.4) was set to exclude M. loti paralog of rimI. Trusted cutoff (80.0) was set at next highest scoring member in the mini-database. [Protein synthesis, Ribosomal proteins: synthesis and modification].	5.51072e-30
NZ_CP030771.1\|WP_138961330.1\|5795064_5796015_-\|DUF389-domain-containing-protein	gnl\|CDD\|129372	TIGR00271, Uncharacterized_protein_MJ0678, uncharacterized hydrophobic domain. This domain is in a family of archaeal proteins that includes AF0785 of Archaeoglobus fulgidus and in several eubacterial proteins, including the much longer protein sll1151 from Synechocystis PCC6803.	1.14297e-52
NZ_CP030771.1\|WP_138961340.1\|5804849_5805965_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD	gnl\|CDD\|236585	PRK09604, PRK09604, tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD.	0
NZ_CP030771.1\|WP_138961331.1\|5796070_5797069_-\|type-I-pantothenate-kinase	gnl\|CDD\|235466	PRK05439, PRK05439, pantothenate kinase; Provisional.	0
NZ_CP030771.1\|WP_138961325.1\|5789343_5790198_+\|tRNA-pseudouridine(38-40)-synthase-TruA	gnl\|CDD\|234577	PRK00021, truA, tRNA pseudouridine(38-40) synthase TruA.	7.97762e-110
NZ_CP030771.1\|WP_138961335.1\|5800711_5801911_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	3.99402e-25
NZ_CP030771.1\|WP_138961328.1\|5793065_5793581_+\|30S-ribosomal-protein-S9	gnl\|CDD\|178888	PRK00132, rpsI, 30S ribosomal protein S9; Reviewed.	4.48709e-73
NZ_CP030771.1\|WP_138961329.1\|5793709_5795068_+\|phosphoglucosamine-mutase	gnl\|CDD\|237672	PRK14318, glmM, phosphoglucosamine mutase; Provisional.	0
NZ_CP030771.1\|WP_138961336.1\|5801929_5802445_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE	gnl\|CDD\|376771	pfam02367, TsaE, Threonylcarbamoyl adenosine biosynthesis protein TsaE. This family of proteins is involved in the synthesis of threonylcarbamoyl adenosine (t(6)A).	6.24504e-46

>NZ_CP030771.1|WP_138961333.1|5797668_5799156_+|NAD(P)H-hydrate-dehydratase
MRTAYRVEDVRAAERALMARVPEGALMQRAAAGLAVACGQLLGKVYGARVALLVGSGDNGGDALYAGARLARRGAGVTAVLLSPERAHAGGLAALRGAGGRVVDGSGAGSGSGSAADAAFASLSGADLVVDGIVGIGGKGGLRPGAAELARAAEESGALVVAVDLPSGVDADTGEVRGAAVRADATVTFGAYKPGLLVDPAREYAGALRLVDIGLGGELSAYAPAVEALQYADVEQLLPVPGAESDKYRRGVLGVVAGSARYPGAAVLTVAGALRGGAGAVRYVGPAADAVIARFPEALVSAGPVPRAGRVQAWVVGPGLGDGHGDAGERLRDVVAAEVPVLIDADGLRLVDASAVRERGAPTLLTPHAGEAAALLGVGRAEVEAARLDAVRELAGRYGATVLLKGSTTLVAGAGGGVVRVNPTGTGWLATAGSGDVLSGLAGALLAAGLGARDAGAVGAFLHGLAGRLAAEGAPVGAQDVAEAVPAAWRDVRRG
>NZ_CP030771.1|WP_138961332.1|5797187_5797556_+|holo-ACP-synthase
MIIGVGIDVAEIDRFAASLERTPGMRERLFVERELHLPGGERRGVASLAARFAAKEALAKALGAPPGLRWTDAEVYVEETGQPRLRVSGTVAARAEALGVRGWHVSLSHDAGVASAVVIAEG
>NZ_CP030771.1|WP_138961331.1|5796070_5797069_-|type-I-pantothenate-kinase
MISLVSSPPRGANRHKPEATPYVDLTRSEWSALREKTPLPLTAAELEKLRGLGDVIDLDEVRDIYLPLSRLLNLYVGATDGLRGALNTFLGDTGEKGSQSGTPFVIGVAGSVAVGKSTVARLLQALLSRWPEHPRVELVTTDGFLLPTKELQARGLMSRKGFPESYDRRALTRFVADIKAGKDEVTAPVYSHLIYDIVPGQRLTVRRPDILIVEGLNVLQPALPGKDGRTRVGLADYFDFSVYVDARAEDIERWYLNRFRKLRETAFQNPSSYFRKYTQVSEEEALDYARTTWRTINKPNLVENVAPTRGRATLIIRKGPDHKVRRLSLRKL
>NZ_CP030771.1|WP_138961330.1|5795064_5796015_-|DUF389-domain-containing-protein
MLHLRLITPADRTDAVVRLIEKTPGTTHLAVVPGAARNPSGDIVMCDVAREAGDELLGGLRALEIDKHGSIALENIDLSLSLRADKAEDEAPGEGADAVLWEHLADATHEESTLSITYVAFITLATMIAACGVVLDNAILIVGAMAVGPEFGPLAGFCTALVQRAPRLALRSLIALIAGFAIAMAVTVAFSFFMDAVDLFDQAALEAKRPNTNFIYRPDWFSFVVAVLAGAAGTLSLTSAKSGALVGVAISVTTVPAAANAAVAFSYDEYRQAWGSTEQLLLNLLGIVLAGTFTLLTQKLLWARQRERTAKKFGLP
>NZ_CP030771.1|WP_138961329.1|5793709_5795068_+|phosphoglucosamine-mutase
MGRLFGTDGVRGVANADLTAELALGLSVAAAHVLAEAGTFEGHRPTAVVGRDPRASGEFLEAAVVAGLASAGVDVLRVGVLPTPAVAHLTAALGADLGVMLSASHNAMPDNGIKFFARGGHKLADDLEDRIESVYEEHRTGAPWERPTGAGVGRVTSYDQGLDQYVAHLIGVLPNRLDGLRIVLDEAHGAAARVSPEAFARAGAEIVTIGASPDGLNINEGCGSTHLELLRAAVVEHGADLGIAHDGDADRCLAVDHTGAEVDGDQILAVLALGMRERGVLRRDTVVATVMSNLGFKLAMEREGLRFVQTAVGDRYVLEEMKANGYALGGEQSGHVIALDHATTGDGTLTGLLLAARVAETGRSLKELAAVMERLPQVLINVPDVDRTRVRTSTELATAVADAERELGETGRVLLRPSGTEPLVRVMVEAADIEQARSVAGRLADVVKSALG
>NZ_CP030771.1|WP_138961328.1|5793065_5793581_+|30S-ribosomal-protein-S9
MAETTAEQPIDETVDIEHYTTESEAPVEGEYTSESNAARFGDPQPAAGLGRRKNAIARVRIVPGTGKWKINGRTLEDYFPNKVHQQEVNEPFKVLELEGRYDVVARIAGGGVSGQAGALRLGVARALNEADVDNNRGALKKAGFLKRDDRAVERKKAGLKKARKAPQYSKR
>NZ_CP030771.1|WP_138961327.1|5792579_5793023_+|50S-ribosomal-protein-L13
MRTYSPKPGDVTRQWHVIDAQDIVLGRLATTAASLLRGKHKPIYAPHVDTGDFVVIINADKVHLSGNKKTQKMAYRHSGYPGGLRSVRYDELLEKNPEKAIEKAVKGMLPKNSLGRQMLSKLKVYKGDQHPHGAQQPQPFEITQVAQ
>NZ_CP030771.1|WP_138961326.1|5791142_5792369_+|DUF2029-domain-containing-protein
MNAGKCDVSGGTGWWLRPAAWQAWAVLGVVLGALVLRVACRVPDGGMDNGIVVRAAGAWLEGRSPYADRHFLYLPGAVLAAVPQAVLPQGVVRALVPLGVVGALAGGWAGALRIHGVPLGSRFAVFGLLGLALGFAPFGHLVELGNWTVASAAALPVALLCVCRGRWGRAGAVLGVAVAVKPLLVPVLLLFVFARRWRELGIAVGVPVAVSAAAALLLPDPAGFLTRTLPFLLRGGDSFVRLYEASPAAVLPRLGVPGAVASLVAGAGAVVGVGCAWRRWGRGDAGAGRVVETAVALMLAAFLVSRPSYDHYLLVVVPLLLAGAGEAGAVVRGAGFWVALVPQVPGFAWVGLEPGVRRAFKDCVTLCVLAFAVARCCLRPRAVTVDDAGPAGPPEAVGSAVPVSRAAF
>NZ_CP030771.1|WP_171075833.1|5790219_5791068_-|hypothetical-protein
MSFGQGGPQWGPGGSTTPDWAALAEASEKRARRRKWLLFGGGALATVAVATAVAVAVVSANGDDAAASNKPASELPSSPDIPGASSAPEPSFEATTPPPPPDPKDYISDADKDKAPLSAAILFPGTKLTSGAKVYKKGATADTKRCASVTQPVLGRVLTKNKCTKLMRVTYARRGIAVTVGVAVFDTEAQAAKVKKQADKGLVTSLPGKGVAPFCRTAVCRGTYNAYGRYAYFTTTGFLGGKDVTEKDRKAYEVGDDLARFAFNQINRRGETQASAAANNPE
>NZ_CP030771.1|WP_138961325.1|5789343_5790198_+|tRNA-pseudouridine(38-40)-synthase-TruA
MSEEVKPGFVRVRLDLSYDGRDFSGWAKQREGQRTVQGEIEDALRTVTRSGETYELTVAGRTDSGVHARGQVAHVDLPESLWAEHREKLLRRLAGRLPHDVRIWRAEEAPAGFNARFSAIWRRYAYRVTDHPGGVDPLLRGHVLWHDWTLDLDAMNEAAQALIGEHDFAAYCKRREGATTIRTLQELRWERRPDGILEATVRADAFCHNMVRSLVGAMLFVGDGHRPPDWPGKVLAAGVRDSAVHVVRPHGLTLEEVGYPADELLAARSAEARNKRSLPSAGCC
>NZ_CP030771.1|WP_138961334.1|5799540_5800698_+|alanine-racemase
MTDTALPRVRAEIDLAALRANVRALRAHAPGAAFMAVVKADGYGHGMVPCAKAALDAGADWVGTATPEEALALRAAGVGGRLMCWLWTPGSPWREAVEADIDVSVSRVQALAEVAAAARAAGRTARVQLKADTGLGRNGCMPDDWPELVGEALRAEADGLVKVTGLWSHFACADEPGHPSIAPQLGTFRSMVGYAEEAGLRPEVRHIANSPATLTLPETHFDLVRPGIAMYGVSPSPEIGTPEDFGLRPVMTVAAALAHVKRAPAGHGVSYGHLYTTAGETTLGLVPAGYGDGIPRHASGTGPVLVGGKWRTVAGRIAMDQFVVDLGGDEPEVGAEAVLFGPGDRGEPTAEDWARAAGTIAYEIVTRIGARVPRVYVNERPGTGD
>NZ_CP030771.1|WP_138961335.1|5800711_5801911_+|alpha/beta-fold-hydrolase
MGEGSTGAAAEVVGAVAGRPGGAVTTWRRAGVAGAAIGVIAAGAAAGVAIERLTVGRGMRKKARLALDASGPYGSLRGTPGKAYADDGTELAFEVDEVGAEGSQAARRRRLFGRRAPAPVTVVFSHGYCLSQDSWHFQRAALRGVVRAVYWDQRSHGRSGRGAARLRDREPVTIDRLGRDLKAVIDAAAPEGPLVLVGHSMGGMTTMALADQFPELIRERVVGVALVGTSAGGLGEVNFGLPVAGVNAVRRVLPGVLRALGSQAELVERGRRATSDLFAGIIKRYSFSSKDVDPAVARFAERMIESTPIDVVAEFYPAFTEHDKADALKHFAELPVLVLAGDKDLVTPSEHSEVIADLLPDAELVLVPDAGHLVMLEHPEVVTDRLADLLARTGAVGTG
>NZ_CP030771.1|WP_138961336.1|5801929_5802445_+|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE
MEAPHSPAVPAATLKIAVNSPEQMGELGRRLAKILRPGDLVMLTGELGAGKTTLTRGLGEGLGVRGAVTSPTFVIARVHPPLGDGPALVHVDAYRLGGGLDEMEDLDLDVSLPDSVVVVEWGDGKVEELSDDRLHLVIHRAVGDTTDEGREITVHGIGARWQDADLSVLAV
>NZ_CP030771.1|WP_138961338.1|5802962_5803511_-|hypothetical-protein
MSRTSSGFVAGLTAAALAVVGFLAYQASASAPDDLNARPDKSPTTPTKSPKGKGGSLALPDRSGTGKRVVYSLEGDRVWLVGDSGKAKRTYKVTPSTVDPEPGTYEVTSRQGQVTGSDGRQIEHVVRFTTVDGITVGFSAALNGSTEKPDPAKKTGGIRSSREDGNAMWDFAIIETPVVVVK
>NZ_CP030771.1|WP_138961339.1|5803613_5804270_+|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB
MLLLALDTATPAVTVALHDGTSVVAESSQVDARRHGELLLPAVDRVLADAGVRLDAVTAVVTGVGPGPYTGLRVGLMTADTFGLALGVPVYGVCTLDGLAYASGIEDGPFVVATDARRKEVYWARYEDPRTRVAGPAVDRPADIAEQVAGLPAVGAGATLYPETFPDARGPEHVAAAALAGLAAEKLAAGEELLEPRPLYLRRPDAQVPKNYKVVTPQ
>NZ_CP030771.1|WP_138966959.1|5804305_5804857_+|ribosomal-protein-S18-alanine-N-acetyltransferase
MRWWDIDPVLALEKELFPEDAWSRGMFWSELAHARGPGSTRRYLVAYDGARLVGYGGLAVAGTDSDGGDALAADVQTIAVARDQWGTGLGARLLTELLRHATAFEATEVMLEVRVDNTRAQKLYERFGFEPIGFRRGYYQPGNVDALVMRLSDPSALPQAPHPSPNGRADGPVNGVQGTEIHG
>NZ_CP030771.1|WP_138961340.1|5804849_5805965_+|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD
MADLRDEPLVLGIETSCDETGVGIVRGTTLLADAVASSVDEHARFGGVVPEVASRAHLEAMVPTIQRALKDAGVAASDLDGIAVTAGPGLAGALLVGVSAAKAYAYALGKPLYGVNHLASHICVDQLEHGALPEPTMALLVSGGHSSLLLSTDITADVRPLGATIDDAAGEAFDKIARVLNLGFPGGPVIDRYAREGDPEAIAFPRGLTGPRDPAYDFSFSGLKTAVARWIEAKRAAGEDVPVRDVSASFQEAVVDVLTRKAVRACKDEGVDHLMIGGGVAANTRLRALAQERCERAGIRLRVPRPKLCTDNGAMVAALGAEMVARNRRPSDLGLSADSSLPVTEPHVPGAHAHTHDHDHVHEVSKDNLYS
>NZ_CP030771.1|WP_138961341.1|5805961_5806216_+|hypothetical-protein
MSVALMWEARAAEGRGPELLAWARAQGLAAAPVRRETFRAPQDRVLVITWWDAAYDAELPELPAPPADLVSRPPHRWRFEPVDS
>NZ_CP030771.1|WP_138961342.1|5806233_5807502_-|class-I-SAM-dependent-methyltransferase
MPRARHRRRTRTFHRLAHNGPVNAPHDPQPATTAFAALLTAEGTALLDAVREVEPAAELAVATRLRRDHPADLVSAALAQARLRQRAVAKFGAGDAARMFFTPNGVEQSTRTSVATYRAERFKELGVRRIADLCGGIGGDAIALARAGIEVLAVDHDPLTCAVARANAAALGLEDLIEVREADVTEVDTAGYDAVFVDPARRGGRGRIFDPEAYSPPLSWAVAAARKAPRAALKIAPGIPHEAVPEEAEAEWISDGGDVKEAVLWFGTDAPGSHRATLLPSRATLCAGRAVMLPDPDVRPVGRYLYEPDGAVIRAHLVAEVAARVEGGLVDETIAYVTSDVARTTPYASAYEITDQLPFNVKKLKALLREREVGVLTVKKRGSAVEPEELRRKVKPRGPGSATVFLTRVAGAPTMLVGHPAP
>NZ_CP030771.1|WP_138961343.1|5807529_5808471_+|polysaccharide-deacetylase-family-protein
MRLVRQNGEWVRMVRGRALLALAALGVGAVASGCASDPDAGAGREHGAPAAHGQQPRLAPPAQALREYAQRLRASQAARAAAAKRWGLAEVPLTAPAAPAVKTRPATRKGFEVRGQAELPPVFTTVPTKDKVVFLTVDDGAEKDPAFLRMMSDLKIPYTAFLSDYLVKEDYGYFKRMRDHGVTLNNHTLNHRYLPGLSYEAQRHEICGMQDVIERRYGKRPELFRPPYGNYNRDTLRAARSCGVKAVPLWASEGFADHMEWREWDKDLHPGDIILTHFRGREDWKGTMPDMVRTVLKTVTDRGYAVARLEDYL

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_15

6205565-6205970

Orphan

Consensus_repeat	Method
GCCCNGCNCCCCGGCGGCCCCNNC	CRT

6 spacers

The CRISPR arrays of NZ_CP030771_15

>merge|NZ_CP030771|15|6205565-6205970|CRT
CCGCCGCGCCCCGGCAGCCCCACCCGACCGACACCCACCCCACCCCCACGGCCCCCGCCCGGGCGACACCCACAGAGCCCGGCTCCCCGGCGGCCCCGGCACCCGACAGCCACCCCGGCGCGCCCGACGCCGCGCCCGCAGTGCCCGGCTCCCTGGCGGCCCAGCCGACCGACGGCCGCCCCGGCCTGTCCGACGCCGCGCCCGGCTCCCCAGCGGCGCCCGACAGCTACCCCGGCGCGGCCGCCCCCGCGCCCGCAGCGCCCGGCTCCCCGGCCGTCCCGGCATCCGACAGTGACCCCAGCCGGACCGCCACACCTGCGCCGCCCGCCCCGGCGGCCCCGCCCGCCCCGGCGGCCCCGGCGGCCCCGGTGGCCCCGGTGGCGGCGTCCGCTCAGGCGGTCGCACC

>NZ_CP030771|15|1|6205565-6205970|CRT
CCGCCGCGCCCCGGCAGCCCCACC	CGACCGACACCCACCCCACCCCCACGGCCCCCGCCCGGGCGACACCCACAGA
GCCCGGCTCCCCGGCGGCCCCGGC	ACCCGACAGCCACCCCGGCGCGCCCGACGCCGCGCCCGCAGT
GCCCGGCTCCCTGGCGGCCCAGCC	GACCGACGGCCGCCCCGGCCTGTCCGACGCCGC
GCCCGGCTCCCCAGCGGCGCCCGA	CAGCTACCCCGGCGCGGCCGCCCCCGCGCCCGCAGC
GCCCGGCTCCCCGGCCGTCCCGGC	ATCCGACAGTGACCCCAGCCGGACCGCCACACCTGC
GCCGCCCGCCCCGGCGGCCCCGCC	CGCCCCGGCGGCCCCGGCGGCCCCGGTGGCCCCGGTGGC
GGCGTCCGCTCAGGCGGTCGCACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138961635.1\|6208955_6210089_-\|P-loop-NTPase	unknown	unknown	gnl\|CDD\|378455
NZ_CP030771.1\|WP_138961637.1\|6210719_6211994_-\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|225148
NZ_CP030771.1\|WP_138961636.1\|6210133_6210730_-\|DUF1003-domain-containing-protein	unknown	unknown	gnl\|CDD\|377629
NZ_CP030771.1\|WP_171075850.1\|6208070_6208817_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961629.1\|6201213_6202014_-\|enoyl-CoA-hydratase/isomerase-family-protein	unknown	unknown	gnl\|CDD\|236163
NZ_CP030771.1\|WP_138961642.1\|6216227_6216869_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961633.1\|6207461_6207935_+\|twin-arginine-translocase-TatA/TatE-family-subunit	unknown	unknown	gnl\|CDD\|179287
NZ_CP030771.1\|WP_138961640.1\|6213558_6214674_-\|magnesium-and-cobalt-transport-protein-CorA	unknown	unknown	gnl\|CDD\|213364
NZ_CP030771.1\|WP_138961628.1\|6200623_6201217_+\|DNA-3-methyladenine-glycosylase-I	unknown	unknown	gnl\|CDD\|377025
NZ_CP030771.1\|WP_171075849.1\|6203561_6204326_+\|RNA-polymerase-sigma-factor-SigE	unknown	unknown	gnl\|CDD\|236606
NZ_CP030771.1\|WP_138961638.1\|6212232_6212994_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961630.1\|6202702_6203401_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|226607
NZ_CP030771.1\|WP_138961639.1\|6213001_6213517_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138961641.1\|6215177_6215768_+\|suppressor-of-fused-domain-protein	unknown	unknown	gnl\|CDD\|377450
NZ_CP030771.1\|WP_138961626.1\|6199153_6200014_-\|dihydropteroate-synthase	unknown	unknown	gnl\|CDD\|273657
NZ_CP030771.1\|WP_016642901.1\|6202289_6202523_+\|DUF3117-domain-containing-protein	unknown	unknown	gnl\|CDD\|371461
NZ_CP030771.1\|WP_138961627.1\|6200174_6200627_+\|DivIVA-domain-containing-protein	unknown	unknown	gnl\|CDD\|274639
NZ_CP030771.1\|WP_138961625.1\|6198337_6199090_+\|TIGR00730-family-Rossman-fold-protein	unknown	unknown	gnl\|CDD\|224527
NZ_CP030771.1\|WP_138961624.1\|6197117_6198209_+\|succinyl-diaminopimelate-desuccinylase	unknown	unknown	gnl\|CDD\|237264
NZ_CP030771.1\|WP_138961631.1\|6204322_6205312_+\|zf-HC2-domain-containing-protein	unknown	unknown	gnl\|CDD\|188261

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138961635.1\|6208955_6210089_-\|P-loop-NTPase	gnl\|CDD\|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	2.63404e-130
NZ_CP030771.1\|WP_138961637.1\|6210719_6211994_-\|CBS-domain-containing-protein	gnl\|CDD\|225148	COG2239, MgtE, Mg/Co/Ni transporter MgtE (contains CBS domain) [Inorganic ion transport and metabolism].	1.0219e-48
NZ_CP030771.1\|WP_138961636.1\|6210133_6210730_-\|DUF1003-domain-containing-protein	gnl\|CDD\|377629	pfam06210, DUF1003, Protein of unknown function (DUF1003). This family consists of several hypothetical bacterial proteins of unknown function.	2.56408e-47
NZ_CP030771.1\|WP_138961629.1\|6201213_6202014_-\|enoyl-CoA-hydratase/isomerase-family-protein	gnl\|CDD\|236163	PRK08140, PRK08140, enoyl-CoA hydratase; Provisional.	1.85583e-76
NZ_CP030771.1\|WP_138961633.1\|6207461_6207935_+\|twin-arginine-translocase-TatA/TatE-family-subunit	gnl\|CDD\|179287	PRK01371, PRK01371, Sec-independent protein translocase protein TatB.	1.85261e-45
NZ_CP030771.1\|WP_138961640.1\|6213558_6214674_-\|magnesium-and-cobalt-transport-protein-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.	1.58689e-166
NZ_CP030771.1\|WP_138961628.1\|6200623_6201217_+\|DNA-3-methyladenine-glycosylase-I	gnl\|CDD\|377025	pfam03352, Adenine_glyco, Methyladenine glycosylase. The DNA-3-methyladenine glycosylase I is constitutively expressed and is specific for the alkylated 3-methyladenine DNA.	1.43056e-103
NZ_CP030771.1\|WP_171075849.1\|6203561_6204326_+\|RNA-polymerase-sigma-factor-SigE	gnl\|CDD\|236606	PRK09647, PRK09647, RNA polymerase sigma factor SigE; Reviewed.	4.21265e-124
NZ_CP030771.1\|WP_138961630.1\|6202702_6203401_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	2.08274e-48
NZ_CP030771.1\|WP_138961641.1\|6215177_6215768_+\|suppressor-of-fused-domain-protein	gnl\|CDD\|377450	pfam05076, SUFU, Suppressor of fused protein (SUFU). SUFU, encoding the human orthologue of Drosophila suppressor of fused, appears to have a conserved role in the repression of Hedgehog signaling. SUFU exerts its repressor role by physically interacting with GLI proteins in both the cytoplasm and the nucleus. SUFU has been found to be a tumor-suppressor gene that predisposes individuals to medulloblastoma by modulating the SHH signaling pathway. Genomic contextual analysis of bacterial SUFU versions revealed that they are immunity proteins against diverse nuclease toxins in polymorphic toxin systems.	8.04563e-30
NZ_CP030771.1\|WP_138961626.1\|6199153_6200014_-\|dihydropteroate-synthase	gnl\|CDD\|273657	TIGR01496, Dihydropteroate_synthase, dihydropteroate synthase. This model represents dihydropteroate synthase, the enzyme that catalyzes the second to last step in folic acid biosynthesis. The gene is usually designated folP (folic acid biosynthsis) or sul (sulfanilamide resistance). This model represents one branch of the family of pterin-binding enzymes (pfam00809) and of a cluster of dihydropteroate synthase and related enzymes (COG0294). Other members of pfam00809 and COG0294 are represented by model TIGR00284. [Biosynthesis of cofactors, prosthetic groups, and carriers, Folic acid].	5.71739e-92
NZ_CP030771.1\|WP_016642901.1\|6202289_6202523_+\|DUF3117-domain-containing-protein	gnl\|CDD\|371461	pfam11314, DUF3117, Protein of unknown function (DUF3117). This family of proteins with unknown function appears to be restricted to Actinobacteria.	5.49792e-25
NZ_CP030771.1\|WP_138961627.1\|6200174_6200627_+\|DivIVA-domain-containing-protein	gnl\|CDD\|274639	TIGR03544, cell_division_initiation_protein_DivIVA, DivIVA domain. This model describes a domain found in Bacillus subtilis cell division initiation protein DivIVA, and homologs, toward the N-terminus. It is also found as a repeated domain in certain other proteins, including family TIGR03543.	1.58142e-06
NZ_CP030771.1\|WP_138961625.1\|6198337_6199090_+\|TIGR00730-family-Rossman-fold-protein	gnl\|CDD\|224527	COG1611, COG1611, Predicted Rossmann fold nucleotide-binding protein [General function prediction only].	2.30365e-56
NZ_CP030771.1\|WP_138961624.1\|6197117_6198209_+\|succinyl-diaminopimelate-desuccinylase	gnl\|CDD\|237264	PRK13007, PRK13007, succinyl-diaminopimelate desuccinylase; Reviewed.	0
NZ_CP030771.1\|WP_138961631.1\|6204322_6205312_+\|zf-HC2-domain-containing-protein	gnl\|CDD\|188261	TIGR02949, putative_anti-sigma_factor, anti-sigma factor, TIGR02949 family. This group of anti-sigma factors are associated in an apparent operon with a family of sigma-70 family sigma factors (TIGR02947). They and appear by homology, tree building, bidirectional best hits and one-to-a-genome distribution, to represent a conserved family. This family is restricted to the Actinobacteria. [Transcription, Transcription factors].	2.33182e-07

>NZ_CP030771.1|WP_138961631.1|6204322_6205312_+|zf-HC2-domain-containing-protein
MSGSRSNPAERHFAEQHLGDRLAALVDGELGHDARERVLAHLATCPTCKTEADAQRRLKSVFAQTAAPPPSESFLARLQNLPGMSLDDIEGQGGPRTPVDDGFATGSSGTTGLPRGGVFSLSGPRPDPLVEYAPSGAHAAVLPSEQRGFRIHAVGRTEAERSGWRGRRFAFAAAGAVSLAAIALGGVTVSAPLGSADQRAGGAGTNSNASPPRSQPAPATGVPESTRRRGGSPFSVQGQRPQAPASTTAAVPLLSGAPGPSTRTPQHLTAPLLAGAGVMSPLVRAAAPDDPERPDVPAGGLTLNAAADPAPRATPPPGLAQRRGTAEIH
>NZ_CP030771.1|WP_171075849.1|6203561_6204326_+|RNA-polymerase-sigma-factor-SigE
MVGAPLDTTRADRGGAAESADQGGALRRFLRLAGRPKSVTDTADRANSAQTATFAADADAQAWTPPTWEEIVSTHSGRVYRLAYRLTGNQHDAEDLTQEVFVRVFRSLSTYTPGTFEGWLHRITTNLFLDMVRRKQRIRFDALGDDAAERLPSREPSPQQVFNDTHFDADVQQALDTLAPEFRAAVVLCDIEGLSYEEIAATLGVKLGTVRSRIHRGRSQLRKALQHRSPEARAERRSLAVTGAVALGGGGATA
>NZ_CP030771.1|WP_138961630.1|6202702_6203401_-|class-I-SAM-dependent-methyltransferase
MCGFPGPTDTVTARQPRGQERAISGNRQTSWAFADAFVAEDEALLWARDRARDAGLRSVSPGTGAALRLLAATVDAKAVAEIGTGTGVSGIHLLHGMRPDGVLTTVDPEPERQQFARMAFRAAGFAGNRARFIPGRALDVLPRLADGGYDLVFCDGDRLECLDYLAESLRLLRPGGLVCFEGVFFDGRTVDSGPQPIEVLRLRELLRAVRESQDLVPSILPVGDGLLCAVKR
>NZ_CP030771.1|WP_016642901.1|6202289_6202523_+|DUF3117-domain-containing-protein
MFDAGDTWVVGCDKLVSGRGTSMAAMKPRTGDGPLEVTKEGRGIVMRVPLEGGGRLVVELTPDEADALGDALKKVVG
>NZ_CP030771.1|WP_138961629.1|6201213_6202014_-|enoyl-CoA-hydratase/isomerase-family-protein
MADTVLYEVSDGLATITLNRPDAMNAMNTEAKVALRDAARAAAADQEVRAVLLTATGRAFCVGQDLKEHIGVLQESRATGSGQTMSTVRDHYNPIVRALTGMAKPVVAGVNGVAAGAGFGFALAADYRVVADTASFTTSFAGVALTADSGVSWTLSRLVGQSRAADLLLFPRSVKAQEALDLGIANKVVPADALAEEARAVARALAEGPTLAYGAIKESLAYAAGHSLDETLDKEDELQTKAGASEDHAIAVQAFLDKAAPRYLGR
>NZ_CP030771.1|WP_138961628.1|6200623_6201217_+|DNA-3-methyladenine-glycosylase-I
MSDAIPGPDGAPRCPWGLSTEDYVAYHDEEWGRPVHGDDALFERLCLEAFQSGLSWITILRRREGFRAAFSGFKIAAVAEFTDTDRERLLADEGIIRNRAKVDATLANARVLADWPEGELDRLIWSFAPDAAARPAPRTLADVPAVTDASTALAKDLKKRGLRFIGPTTAYALMQACGLVNDHLADCVAREASGSGR
>NZ_CP030771.1|WP_138961627.1|6200174_6200627_+|DivIVA-domain-containing-protein
MVMFLFLVVALVVVVAAVTLAVLGGSEGGTLPDVPPERFADPLPPDRPLRRADVEAVRFPMTVRGYRMVDVDEALDRLGAELAERDARIAELETALAGAQATAVGGPGLFTTYAGPPAPAPDPAEHGPSDRVPDGEDPAAPHAERPEDDR
>NZ_CP030771.1|WP_138961626.1|6199153_6200014_-|dihydropteroate-synthase
MLKLGRRVFEAHEPVIMAIVNRTPDSFYDQGATFRDEPALARVEQAVAEGAAIIDIGGVKAGPGEEVTAAEEARRTVGFVAEVRRRFPDVVISVDTWRHEVGEAVCDVGADLLNDAWGGVDPKLAEVAARYGVGLVCTHAGGAEPRTRPHRVTYEDVVADILRVTVGLAERAVELGVPRESVLIDPGHDFGKNTRHSLEATRRLGELVDTGWPVLVSLSNKDFVGETLDRPLKERVVGTLATTAVSAWLGAQVYRVHEVAETRQVVDMVATIAGHRPPAVARRGLA
>NZ_CP030771.1|WP_138961625.1|6198337_6199090_+|TIGR00730-family-Rossman-fold-protein
MGSPEAQGPPEEQHLGPVVRRREQITPGTTDQRLLDTEGGDSAWVHTDPWRVMRIQSEFVEGFGALAELPSAISVFGSARTRPDSPEYEAGVRIGKALVEAGFAVITGGGPGAMEAANKGAREAKGVSVGLGIELPFEQGLNPHVDIGVNFRYFFVRKTMFVKYAQGFVVLPGGLGTLDELFEALTLVQTRKVTRFPIVLFGSAYWGGLVDWLRDTVVAQGKASEHDLLLFHVTDDVDEAVSLVTKEVGR
>NZ_CP030771.1|WP_138961624.1|6197117_6198209_+|succinyl-diaminopimelate-desuccinylase
MDQTSAQPPLDLTMDAAALTAALVDFPSPSGQEKALADAIETALRALPHLTVDRHGNNVVARTDLGRAERVVLAGHIDTVPIAGNVPSRLDEDGVLWGCGTCDMKSGVAVQLRIAQTVPEPNRDLTFVFYDNEEVAAHLNGLGHVAEAHPDWLAGDFAVLLEPTGNQVEGGCQGTLRVHLKTTGERAHSARAWMGSNAIHAAAPILAKLAAYEARRPVVDGLQYHEGLNAVGIEGGVATNVIPDACTVVVNFRYAPDRTPEEAEAFVRDYFADCGIDEFVVDDHTGGARPGLTHPSAQAFLAAVGGEARPKYGWTDVARFSALGVPAVNYSPGEPLLAHKVDERVKASLIPEAEAKLRAWLTS
>NZ_CP030771.1|WP_138961633.1|6207461_6207935_+|twin-arginine-translocase-TatA/TatE-family-subunit
MFNDIGVFEIVTLVILAVLIFGPDKLPKFIQDASRTIRKIRQFSDSAKQDIRDELGPEFKDFEFDDLNPKKFIRKQMERDDLGLKEIRNGFDLRKEMAEVADSVHGRESESGQDRADGASRSGTSTASANGSGRIDMEKRPAKPAADDHPPFDADAT
>NZ_CP030771.1|WP_171075850.1|6208070_6208817_+|hypothetical-protein
MSGVRTPEGGGPLRTDDSEEAAGYMETTSRVGAQASAADGTASQAVPSARRTVDGYLLAPFPWYGLDEAFTGPRWLMQVGTAADGAVEHGSIGHGDEPSVRAEGGLGNGDRERFAVVVTVAANPVRRSADGTGVLEATSVSSAAWLAGVGLLSYTWPGQMDHSLRDDWLDQQTETAWVLADDLDGSDWSSLSLPVDGVPTSFHYRESEYGWVLAGSTQEGVHLGAYGRGMSAYGLGFSVVKDIAAYAK
>NZ_CP030771.1|WP_138961635.1|6208955_6210089_-|P-loop-NTPase
MVTEDAVREALATVNDPEIQRPITELGMVKSVDIGADGAVAVAVYLTVSGCPMRDTITKNVTDAVARVEGVTRVDVTLDVMSDEQRKELATALRGGQAEREVPFAKPGSLTRVYAVASGKGGVGKSSVTVNLAAAMAADGLKVGVVDADIYGHSVPRMLGADGRPTQVENMIMPPSANGVKVISIGMFTPGNAPVVWRGPMLHRALQQFLADVFWGDLDVLLMDLPPGTGDIAISVAQLVPNAEILVVTTPQQAAAEVAERAGSIAVQTHQKIVGVVENMSGLPCPHCGEMVDVFGTGGGQRVAEGLTKTTGATVPVLGSIPIDVRLREGGDEGRPVVLSDPESPAGSALRTIAGKLGGRQRGLSGLSLGITPRNKF
>NZ_CP030771.1|WP_138961636.1|6210133_6210730_-|DUF1003-domain-containing-protein
MARERQGRVGGREREAREERREPRPETRPRFRLDQPRARRRKLLPDYDPEAFGRLSERIARFLGTGRFIVWMTVVIIMWVVWNVSAPESLRFDNYPFIFLTLMLSLQASYAAPLILLAQNRQDDRDRVTHEQDRRQNERSIADTEYLTRELASLRMGLGEVATRDWLRSELQDLVKELEEQRPVFPPEAARARDVGDR
>NZ_CP030771.1|WP_138961637.1|6210719_6211994_-|CBS-domain-containing-protein
MAGGAPRIFVSHLSGTAVFDPNGDQVGRVRDLVVMLRVGRRPPRLLGLVVELATRRRIFLPMTRVTGIESGEVISTGVLNVRRFEQRPTERLVLGEMLDRRVRLVETGEEVTVLDVSVRQLPARRDWEVDRVFVRKGKEGAFRRKGETLTVDWSAVDGFSLEEHGQGAENLLATFEQLRPADLANVLHHLSAKRRAEVAAALDDDRLADVLEELPEDDQIEILGKLKEERAADVLEAMDPDDAADLLAELPEDDKERLLTLMQPDDAADVRRLMAYEERTAGGLMTTEPIVLRPDATVADALARVRQEDLSPALAAQVYVCRPPDETPTGKYLGTVHFQRLLRDPPYTLVGSILDDDLRPLSPEDQLPVVAGFFAAYDMVAAPVVDEGGALLGAVTVDDVLDHMLPEDWRETEFHLQEEAGHGA
>NZ_CP030771.1|WP_138961638.1|6212232_6212994_+|hypothetical-protein
MRPAPRFRRSALLGAVCAGLVVGGAGLTACGGGGEDPDQGTNGVGKLSAARIQSKARQAAEAAPAVRLSGSVVTKGHTYKLDMRLTANGGTGTVTSKGQMFELLRVGENLFLKADSAFWAHEGEDGGSPGADSSAAAKLDGKYVKVPQGDPAYRRLSGFTDKDVLLDGTLALHGTLAKGERGGSGSKRYIRISGDEGAGGTLEVSLDGKPYPLTLRRAGGAGTLRLSEWNQAVPLKEPGLNETVDYGKQLPTS
>NZ_CP030771.1|WP_138961639.1|6213001_6213517_-|hypothetical-protein
MTADTLFGRALIEEATKKSGLIWVRGAGPARALWHVWLDGAAHLVGDGPGEQPLPHLADGATAEVTVRSKDKGGRLLSWTATVTELAPRTEEWEAAVAELKGKRLNAPDGERVVERWAAECRVLRLTPREADLEPPGGSLAAPPLPTPATTRRPMPQALPKLLLGRGRKRR
>NZ_CP030771.1|WP_138961640.1|6213558_6214674_-|magnesium-and-cobalt-transport-protein-CorA
MSMIRDLRAAVRPSLRKDSGAYSSYDATRDPRAASAVVDCAVYRDGRRVSCDETLTPHEAMLQVRRDGGFAWIGLHEPTEAEFAGIAAEFGLHPLAVEDAVHAHQRPKLERYDDTLFTVFKTIHYVEHAELTATSEVVETGEVMCFTGRDFFITVRHGGHGSLRALRRRLQDEPELLAKGPSAVLHTIADHVVDGYLAVADAMQVDIDDVENEVFAATGKGGSRGVDAGRIYQLKREVLEFKRAVQPLLRPMQLLSERPMRLVDPDIQKYFRDVADHLARVQEQVLGFDELLNSILQANLAQAAVAQNEDMRKITSWAAIIAVPTAVCGVYGMNFDHMPELHWRFGYPMVLGLIATACYSIHRTLKRNGWL
>NZ_CP030771.1|WP_138961641.1|6215177_6215768_+|suppressor-of-fused-domain-protein
MADVLALVEARLRDGLGEPDARAAVTFLGTDRVEVLRFPAESTGVVRYATLGMSAQPMADPTAVLADPVKGPRAELVLSVRGGVADTDKVLRPLAVLAASPQVEGVVVAPGSSLDVGEPLWPGAPFTSVLVAEPGGLVADLELAEPMEPVRFLPLLPMTPNEAAWKRVHGAQALQERWLSKGTDLRDPLRAGVALD
>NZ_CP030771.1|WP_138961642.1|6216227_6216869_+|hypothetical-protein
MRGEPSCPKCGGRVRAPGLFADSWQCDVHGTVHPLQPVIPPSVEALSVVVHRAQVPVWMPWPLPVGWLFTGVACAGDDRSGGRATAVACSGPAPLGGGGELILVAEELGVGLGARYAGIDGPDPGPGMNVGKPPAAKVLAAGRPTPMWHVSGTPEDRAVFAGEACGLWLWAVAWPEQSGLLMYDELVLTDLRDAGAEVELLPCGALSPRLLTP

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_16

7641758-7641990

Orphan

Consensus_repeat	Method
GCCTGCCGAGGCCACGGGGCCCACCG	CRISPRCasFinder

4 spacers

The CRISPR arrays of NZ_CP030771_16

>merge|NZ_CP030771|16|7641758-7641990|CRISPRCasFinder
GCCTGCCGCGGCGACCGGGGCGGTCGGTGGTGCCGGGGCTTCCAGGGCTGCCGTGAGGAGGGGGCCCCTCGGGGTGGCCGGGTCCACCGGGTCACTCGAGCCTGCCGAGGCCACGGGGCCCACCGAGTCTGCCGAGGCCACGGGGGCGACCGGGCCTGCCGAGGCCACGGGGCCGACCGGGCCTGCCGAGGCCATGGGGTGCGTTGGGCCTGCCGAGGCCATGGGACCTGCCG

>NZ_CP030771|16|14|7641758-7641990|CRISPRCasFinder
GCCTGCCGCGGCGACCGGGGCGGTCG	GTGGTGCCGGGGCTTCCAG
GGCTGCCGTGAGGAGGGGGCCCCTCG	GGGTGGCCGGGTCCACCGGGTCACTCGA
GCCTGCCGAGGCCACGGGGCCCACCG	AGTCTGCCGAGGCCACGGGGGCGACCGG
GCCTGCCGAGGCCACGGGGCCGACCG	GGCCTGCCGAGGCCATGGGGTGCGTTGG
GCCTGCCGAGGCCATGGGACCTGCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138962650.1\|7628288_7628966_+\|FCD-domain-containing-protein	unknown	unknown	gnl\|CDD\|224715
NZ_CP030771.1\|WP_138962649.1\|7627241_7628189_+\|beta-ketoacyl-ACP-synthase-3	unknown	unknown	gnl\|CDD\|236475
NZ_CP030771.1\|WP_138967285.1\|7650648_7651899_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340911
NZ_CP030771.1\|WP_171075896.1\|7626956_7627118_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138962657.1\|7639722_7641153_+\|ThuA-domain-containing-protein	unknown	unknown	gnl\|CDD\|377643
NZ_CP030771.1\|WP_138962659.1\|7645010_7645709_+\|EboA-domain-containing-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138967283.1\|7642765_7643944_+\|UbiA-family-prenyltransferase	unknown	unknown	gnl\|CDD\|260127
NZ_CP030771.1\|WP_138962661.1\|7646560_7647766_+\|metabolite-traffic-protein-EboE	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138962664.1\|7652182_7653571_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340911
NZ_CP030771.1\|WP_138962654.1\|7634492_7635842_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP030771.1\|WP_138962658.1\|7643940_7645014_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138962660.1\|7645708_7646557_+\|TatD-family-hydrolase	unknown	unknown	gnl\|CDD\|224024
NZ_CP030771.1\|WP_138962662.1\|7647762_7649163_+\|alkaline-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|366747
NZ_CP030771.1\|WP_138962655.1\|7635941_7636940_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138962663.1\|7649364_7650465_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP030771.1\|WP_138962665.1\|7653705_7655862_-\|acetate--CoA-ligase-family-protein	unknown	unknown	gnl\|CDD\|131764
NZ_CP030771.1\|WP_138962656.1\|7637259_7639707_+\|PQQ-dependent-sugar-dehydrogenase	unknown	unknown	gnl\|CDD\|271150
NZ_CP030771.1\|WP_138962652.1\|7632332_7633352_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224093
NZ_CP030771.1\|WP_138962653.1\|7633376_7634426_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|380534
NZ_CP030771.1\|WP_138962651.1\|7629351_7630533_+\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138962650.1\|7628288_7628966_+\|FCD-domain-containing-protein	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	4.08701e-48
NZ_CP030771.1\|WP_138962649.1\|7627241_7628189_+\|beta-ketoacyl-ACP-synthase-3	gnl\|CDD\|236475	PRK09352, PRK09352, beta-ketoacyl-ACP synthase 3.	1.86811e-154
NZ_CP030771.1\|WP_138967285.1\|7650648_7651899_-\|MFS-transporter	gnl\|CDD\|340911	cd17353, MFS_OFA_like, Oxalate:formate antiporter (OFA) and similar proteins of the Major Facilitator Superfamily of transporters. This subfamily is composed of Oxalobacter formigenes oxalate:formate antiporter (OFA or OxlT) and similar proteins. O. formigenes, a commensal found in the gut of animals and humans, plays an important role in clearing dietary oxalate from the intestinal tract, which is carried out by OFA/OxlT, an anion transporter that facilitates the exchange of divalent oxalate with monovalent formate, the product of oxalate decarboxylation. This exchange generates an electrochemical proton gradient and is the source of energy for ATP synthesis in this cell. The OFA-like subfamily belongs to the Monocarboxylate transporter -like (MCT-like) family 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.	7.32164e-100
NZ_CP030771.1\|WP_138962657.1\|7639722_7641153_+\|ThuA-domain-containing-protein	gnl\|CDD\|377643	pfam06283, ThuA, Trehalose utilisation. This family consists of several bacterial ThuA like proteins. ThuA appears to be involved in utilisation of trehalose. The thuA and thuB genes form part of the trehalose/sucrose transport operon thuEFGKAB, which is located on the pSymB megaplasmid. The thuA and thuB genes are induced in vitro by trehalose but not by sucrose and the extent of its induction depends on the concentration of trehalose available in the medium.	3.41672e-111
NZ_CP030771.1\|WP_138967283.1\|7642765_7643944_+\|UbiA-family-prenyltransferase	gnl\|CDD\|260127	cd13964, PT_UbiA_1, UbiA family of prenyltransferases (PTases), Unknown subgroup. Many characterized members of the UbiA prenyltransferase family are aromatic prenyltransferases and play an important role in the biosynthesis of heme, chlorophyll, vitamin E, and vitamin K. They contain two copies of a motif similar to the active site DxxD motif of trans-prenyltransferases and are potentially related. Prenyltransferases (PTs) catalyze the regioselective transfer of prenyl moieties onto a wide variety of substrates and play an important role in many biosynthetic pathways. The function of this subgroup is unknown.	4.61694e-42
NZ_CP030771.1\|WP_138962661.1\|7646560_7647766_+\|metabolite-traffic-protein-EboE	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	5.53091e-08
NZ_CP030771.1\|WP_138962664.1\|7652182_7653571_-\|MFS-transporter	gnl\|CDD\|340911	cd17353, MFS_OFA_like, Oxalate:formate antiporter (OFA) and similar proteins of the Major Facilitator Superfamily of transporters. This subfamily is composed of Oxalobacter formigenes oxalate:formate antiporter (OFA or OxlT) and similar proteins. O. formigenes, a commensal found in the gut of animals and humans, plays an important role in clearing dietary oxalate from the intestinal tract, which is carried out by OFA/OxlT, an anion transporter that facilitates the exchange of divalent oxalate with monovalent formate, the product of oxalate decarboxylation. This exchange generates an electrochemical proton gradient and is the source of energy for ATP synthesis in this cell. The OFA-like subfamily belongs to the Monocarboxylate transporter -like (MCT-like) family 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.	1.56596e-108
NZ_CP030771.1\|WP_138962654.1\|7634492_7635842_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	4.7493e-59
NZ_CP030771.1\|WP_138962658.1\|7643940_7645014_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	6.50898e-29
NZ_CP030771.1\|WP_138962660.1\|7645708_7646557_+\|TatD-family-hydrolase	gnl\|CDD\|224024	COG1099, COG1099, Predicted metal-dependent hydrolases with the TIM-barrel fold [General function prediction only].	2.48329e-89
NZ_CP030771.1\|WP_138962662.1\|7647762_7649163_+\|alkaline-phosphatase-family-protein	gnl\|CDD\|366747	pfam01663, Phosphodiest, Type I phosphodiesterase / nucleotide pyrophosphatase. This family consists of phosphodiesterases, including human plasma-cell membrane glycoprotein PC-1 / alkaline phosphodiesterase i / nucleotide pyrophosphatase (nppase). These enzymes catalyze the cleavage of phosphodiester and phosphosulfate bonds in NAD, deoxynucleotides and nucleotide sugars. Also in this family is ATX an autotaxin, tumor cell motility-stimulating protein which exhibits type I phosphodiesterases activity. The alignment encompasses the active site. Also present with in this family is 60-kDa Ca2+-ATPase form F. odoratum.	1.83017e-70
NZ_CP030771.1\|WP_138962655.1\|7635941_7636940_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	6.60435e-30
NZ_CP030771.1\|WP_138962663.1\|7649364_7650465_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.95093e-26
NZ_CP030771.1\|WP_138962665.1\|7653705_7655862_-\|acetate--CoA-ligase-family-protein	gnl\|CDD\|131764	TIGR02717, Uncharacterized_protein_MJ0590, acetyl coenzyme A synthetase (ADP forming), alpha domain. Although technically reversible, it is believed that this group of ADP-dependent acetyl-CoA synthetases (ACS) act in the direction of acetate and ATP production in the organisms in which it has been characterized. In most species this protein exists as a fused alpha-beta domain polypeptide. In Pyrococcus and related species, however the domains exist as separate polypeptides. This model represents the alpha (N-terminal) domain. In Pyrococcus and related species there appears to have been the development of a paralogous family such that four other proteins are close relatives. In reference, one of these (along with its beta-domain partner) was characterized as ACS-II showing specificity for phenylacetyl-CoA. This model has been constructed to exclude these non-ACS-I paralogs. This may result in new, authentic ACS-I sequences falling below the trusted cutoff.	6.51588e-160
NZ_CP030771.1\|WP_138962656.1\|7637259_7639707_+\|PQQ-dependent-sugar-dehydrogenase	gnl\|CDD\|271150	cd04084, CBM6_xylanase-like, Carbohydrate Binding Module 6 (CBM6); many are appended to glycoside hydrolase (GH) family 11 and GH43 xylanase domains. This family includes carbohydrate binding module 6 (CBM6) domains that are appended mainly to glycoside hydrolase (GH) family domains, including GH3, GH11, and GH43 domains. These CBM6s are non-catalytic carbohydrate binding domains that facilitate the strong binding of the GH catalytic modules with their dedicated, insoluble substrates. Examples of proteins having CMB6s belonging to this family are Microbispora bispora GghA, a 1,4-beta-D-glucan glucohydrolase (GH3); Clostridium thermocellum xylanase U (GH11), and Penicillium purpurogenum ABF3, a bifunctional alpha-L-arabinofuranosidase/xylobiohydrolase (GH43). GH3 comprises enzymes with activities including beta-glucosidase (hydrolyzes beta-galactosidase) and beta-xylosidase (hydrolyzes 1,4-beta-D-xylosidase). GH11 family comprises enzymes with xylanase (endo-1,4-beta-xylanase) activity which catalyze the hydrolysis of beta-1,4 bonds of xylan, the major component of hemicelluloses, to generate xylooligosaccharides and xylose. GH43 includes beta-xylosidases and beta-xylanases, using aryl-glycosides as substrates. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold.	2.42083e-38
NZ_CP030771.1\|WP_138962652.1\|7632332_7633352_+\|ABC-transporter-permease	gnl\|CDD\|224093	COG1172, AraH, Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components [Carbohydrate transport and metabolism].	3.80143e-82
NZ_CP030771.1\|WP_138962653.1\|7633376_7634426_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|380534	cd06311, PBP1_ABC_sugar_binding-like, periplasmic sugar-binding domain of uncharacterized ABC-type transport systems. Periplasmic sugar-binding domain of uncharacterized ABC-type transport systems that share homology with a family of pentose/hexose sugar-binding proteins of the type 1 periplasmic binding protein superfamily, which consists of two domains connected by a three-stranded hinge. The substrate specificity of this group is not known, but it is predicted to be involved in the transport of sugar-containing molecules and chemotaxis.	5.48744e-82
NZ_CP030771.1\|WP_138962651.1\|7629351_7630533_+\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	7.98946e-70

>NZ_CP030771.1|WP_138962657.1|7639722_7641153_+|ThuA-domain-containing-protein
MRVRARLVVATAAATLLIGCVSGPARSRPDPDDGGRTGGKDGERVLVFSKTAGFRHDSIPDGIAAVRDLGAAHGFSVDATDDARAFTPKNLSRYDAVVWLSTTGDVLNSAQQTAFERYVRAGGGYVGVHAAADTEYDWPFYGALVGAHFQSHPAVQPAKIKVEDHAHPATAHLGAGWDRTDEWYNYRSNPRTRARVLASLDESSYSGGSMGGDHPIAWCQSSVDGGAGRSFYTGGGHTRQSYAAPAFRRHLLGGIQYATGAARADCRPEQGYTSLFDGTAASLTRWKQAGPGSFALADDGTLTSVGGMGLFWYAHRSFASYSLKLDWKMTGADKDDNSGVFVGFPPSDDPWSAVNNGYEIQIDATDVPEKTTGSVYGFKSADLSARDRALNPPGQWNTYELRVEGERLRIWLNGTLINDYTNTEPARSLLDGHIGIQNHGADDQVAFRDIRVKDLAAARSTDASATAPEARGAGAR
>NZ_CP030771.1|WP_138962656.1|7637259_7639707_+|PQQ-dependent-sugar-dehydrogenase
MHRPRPTPRKALALLTGTLLTAATLTVAAPHSTAQAPSQPRAEDFQQVTLAKGEPEMGEPMTLAVLPDRSVLHTSRDGTVRLTDAKGETKVAGRIPVYSHDEEGLQGVGVDPNFRKNRAVYLYYAPPLSTPAGDAPNDGTAADFKKFDGVNRLSRFVLKPDGTLDLAGEKKVIDVPASRGICCHVGGDIDFDKQGNLYLSTGDDSNPFASDGYTPIDERAGRNPAYDAQRTAANTNDLRGKILRIKVRDDGSYAVPRGNLFAKGTAKTRPEIYAMGFRNPFRMSVDKPTGIVYLGDYGPDAGKADPKRGPAGQVEFTRVTKPGNYGWPYCTGKNDAYVDYDFATGASGAAFDCAAPRNTSPRNTGLTRLPPAQPAWIPYDGGSVPEFGTGSESPMGGPVYRYDANLASPVKFPQAYDGNYFAGEFGRRWIKRIDQGADGAVKSINAFPWKGTQVMDMEFGPDGALYVLDYGTGYFNGDQNSALYRIENATGGHSPVVEAAASVTSGQIPLKTQFTARATDADGDALTYAWDFGDGGTSTEQNPSHTYDKNGVYTATVTAKDPGGRTGTASAHVTVGNTAPTVKLELPGDGQLFTFGDKVPFKVTVTDPEDGTVDCSKVKVTHILGHDSHGHPVTSANGCEGTVQTSADSEHDPNANIFGVFDAEYTDKGANGQPPLTTHDQSVTQTRHRQAEHYGASQGVSVISHTPAHGGKTVGDIHNGDWISFKPYQLGNATKLTARVASAGSGGTLEIRAGAADGTLLGSAKVDPTGSWETYTDVSTAIAGAPTGTTTLYLVFKGAGTGALYDVDDFTFTTS
>NZ_CP030771.1|WP_138962655.1|7635941_7636940_+|TIM-barrel-protein
MPRSFTLFTGQWADLPLEEVCSLARDFGYDGLELACWGDHFEVDKALADPSYADGRRALLDKYGLKCWAVSNHLVGQAVCDAIIDERHRAILPARIWGDGDAEGVRRRAAAEMADTARAAAAFGVRTVVGFTGSAIWHLVAMFPPAPEAMIERGYEDFAERWNPILDVFDAEGVRFAHEVHPSEIAYDYWTTQQALDAVGHRPAFGLNFDPSHFVWQDLDPVSFLWDFRERVYHVDCKEARRRLDGRNGRLGSHLPWGDPRRGWDFVSAGHGDVPWEDVFRMLRAISYDGPISVEWEDAGMDRLQGAPEALRHLKSYDYEPPTASFDAAFAK
>NZ_CP030771.1|WP_138962654.1|7634492_7635842_+|Gfo/Idh/MocA-family-oxidoreductase
MSETEHEAASGAAASGAAASGAVPTGGPAAARRRLGVGMVGYAFMGAAHSQGWRTVGRVFDLPVEARLAAVCGRHGAAVRAAADRLGWAAAETDWRALIARDDVDLVDVCTPGDSHAEIAIAALEAGKHVLCEKPLANTVEEAEAMAAAAERARARGQMAMVGFNYRRVPALVLAREMVAAGRLGTLRHVRLTYLQDWLVDPGFPLTWRLRRDRAGSGALGDLGAHIVDLAQYLTGEAVAGVSALTETFVRERPLLEGTSSGLAAGGAGTGGGGAAGAEAGGTGADGGGAGRAAVGQVTVDDAAVFTARFPSGALATFEATRFAAGRKNALRLELNGSDGSLAFDLERLNELSFHDHTEPAASAGFRRILVTESAHPYLAAWWPPGHGLGYEHTFVHQARDLLHAIATGTAPEPSFADGLAVQRVLAAVEESAQKNSVYTPVAAAPAAT
>NZ_CP030771.1|WP_138962653.1|7633376_7634426_+|substrate-binding-domain-containing-protein
MPHSTSRRGLLFGAAAVSAGAVLTGCTSNESKDSDGDAAPAGDNRPADDKPGKEVTIGFAGPQADHGWLNAINDNAKERAEKYKDVTLEATEGSNDTAAQIGQVETLINKKVDVLVILPADGKALTRVGLKAMKAGIPVVNLDRIFASAQAYRCWIGGDNYGMGLNAGHYIGEKLKGTKNARVVELAGLDNLELTKQRTKGFDDALKNYPNIEKVARQAAEFTVESGQAKMAQLLQAQKNIDALWNHDDDQGVGALRAIKQAGRDDFLMVGGAGALSAFQEIKADRGVLKATVLYPPTMAASAIDLARALGQGKGIGGMAEYEIPASITLYSAVVDKDNVDQYMSTGFK
>NZ_CP030771.1|WP_138962652.1|7632332_7633352_+|ABC-transporter-permease
MTQPASPARPVTEKSPPADGERGPLWALAARVDLRTLSLLGVLAVLIVIGGVTQPDAFLDTDNVQLILTQASVIGVVTVGMTFVIISGGIDLSVGAIVALASVWATTVATQEYGFAGILFTAVVVGLGCGLVNGLLIAYGGLVPFIATLAMLASGRGLALEITDGKTQMVTVDGVLKLGERDAYVLGIPPLVLVFAGVTLLGWLLLNRTTFGRRSVAVGGNAEAARLAGIDVRRQRLYLYLLSGLCCGIAAFLLIVLSGSGQNTNGNLYELDAIAAAIIGGTLLSGGRGTITGSVLGVLIFTTITNIFALNNLETAVQQIAKGAIIVAAVLVQRRTATT
>NZ_CP030771.1|WP_138962651.1|7629351_7630533_+|ROK-family-protein
MTARPANAHQARLLRLLRDDGPNSRAQLGDQVDLSRSKLAVEVDRLLETGLVVADGLAASRGGRRSHNIRLAPNLRFLGVDIGATSVDVAVTNAELEVLGHLNQPMDVREGPVAVFEQVLAMAAKLRASGLAEGFDGAGIGVPGPVRFPEGVPVAPPIMPGWDGFPVREALSQELGCPVMVDNDVNLMAMGEQHAGVARSVGDFLCVKIGTGIGCGIVVGGQVYRGTTGSAGDIGHIQVEPEGRPCACGNKGCLEAHFSGAALARDAREAAHQGRSPELAARLEAAGALTAADVAAAAAAGDPTALDLIRAGGNRTGQVIAGLVSFFNPGLVVIGGGVTGLGHTLLAAIRTQVYRQSLPLATGNLPIVLGELGPAAGVTGGARLISDHLFSPA
>NZ_CP030771.1|WP_138962650.1|7628288_7628966_+|FCD-domain-containing-protein
MLSAGLPQGTVPKLERPGPLRERVYEALLELITTRALRPGQHLVESELAGHLGVSRQPVREALQRLNTEGWVDLRPAQGAFVHEPTEEEADQLLTVRTLLEAEAARLAAANAGSAGIAALEELCARGESAVAAGDVDLVVATNAAFHAKVMELAGNVVLAELAGRVDGRVRWYYTPVARQRGIRSWVEHRELIAAIAARDEARATAVMRAHTEHTRRTYHDRTPA
>NZ_CP030771.1|WP_138962649.1|7627241_7628189_+|beta-ketoacyl-ACP-synthase-3
MPGSRIAAVGHYQPAKVLTNDDLAGMVDTSDAWIRSRVGIRTRHIAGPEEPVDELAAHAAAKALAAAGRAPASVDLVVVATSTAVDRSPNMAARVAARLGLPSPAALDVNVVCAGFTHALATADHAVRAGAASRAVVIGADKMSEITDWTDRTTCVLVGDGAGAAVVEACGEGEEPGISPVLWGSVPEMGHAVRIEGQPARFAQEGQSVYRWATTQLPPLARATCERAGLTPADLAAVVLHQANLRIVEPLATRIGAVNAVVARDVVDSGNTSAASVPLALSKLVERGEIVTGDPVLLFGFGGNLSYAGQVVRCP
>NZ_CP030771.1|WP_171075896.1|7626956_7627118_+|hypothetical-protein
MTTPPSPPPADGGAPGPPPRRRALILGSWLWVTVPLAYGLYELVHKARQLFTG
>NZ_CP030771.1|WP_138967283.1|7642765_7643944_+|UbiA-family-prenyltransferase
MRLPALFTVPGDALAGAAATGLRPGRGTALALTSSLCLYEAGMALNDWADRAEDAVDRPHRPIPSGRVHPAAALTAAAALTAAGLALAARAGRPALTVATALAGTVWAYDLTLKHTKAGPTAMATARALDLLLGATATATASGVVAGRVGAGPGATGATAGGSAAGATGTREGMSRVSSALPAALALGAHTLAVTSVSRHETQGGSTTAPLGALATTLALAHAVARPRRTADGPPSHRRAVHGPPSLPQPTDGPLSLPRSADGPPALPQSAGGPPSLPQSADGPPALPADRRPAVRLGLPGTTRPARPAEDTGALTRTALALAYTATAGRPFLHAALNPSPPLTQRAVGGGIRALIPLQAALAARSGALGSALVAASLAPAARRFARRVSVT
>NZ_CP030771.1|WP_138962658.1|7643940_7645014_+|TIM-barrel-protein
MTAANETPPARGASRLDSPRAGAPAAQEAPAAGLPAEGAPAPLRFGYGTNGLTDLRLDDALGLLADLGYSGVGLTLDHMHLDPLAPDLAARTRRVARRLDRLGLTVTVETGARYVLDPRRKHGPSLLDPDPQGRAERARLLVRAVQVATDLGAHAVHCFSGITPDGTSVDTAWSRLTDALVPVLDAASQARLPLAVEPEPGHLLATLADFHHLRHLLGDPEPLGLTLDIGHCQCLEPRSPADCVRAAAPWLRHVQIEDMRRGVHEHLPFGDGEIDFPPVLRALADTGYQGLTVVELPRHSHAGPQLAAQSLDFLRRAAPVARPQPETCGTHTSPRAPSSPVTVPLPLREASPRGGTP
>NZ_CP030771.1|WP_138962659.1|7645010_7645709_+|EboA-domain-containing-protein
MTDTSAVADLRSRLDATLGGAARAWLDQAVAEATAHPTADDRAAHSMWELRFAEAGRRCGPEHADAARLLLLHAARADTATLTRLYDQGTAAERRAVLRSLPLLVSGPDALPLVDDALRTNDTRLLAAALGPYAAAHLPAHTWRHAVLKCLFTGVPVDAVADLERRAHADAELARMLADYADERTAAGRPVPGDLRRVLALAAPPDPSDLPDPVASVTVTAPSTPIGEEQES
>NZ_CP030771.1|WP_138962660.1|7645708_7646557_+|TatD-family-hydrolase
MRIFDPHIHMSSRTTDDYQAMHAAGVRAVVEPAFWLGQPRTSPASFVDYFDSLLGWEPFRAAQYGIAHHCTIALNPKEANDARCTPVLDLLPRYLVKDNVVAVGEIGYDSMTPAEDTALAAQLQLAADHELPALVHTPHRDKLAGLRRTLDVVAESALPLDRVLIDHLNETTVKEAKDAGCWLGFSIYPDTKMDEERMVAILRQYGPEHVLVNSAADWGRSDPLKTRKVGDAMLDAGFTEDDVDRVLWRNPVAFYGLSGRLSLDVTDTDATHEGNSILRGGA
>NZ_CP030771.1|WP_138962661.1|7646560_7647766_+|metabolite-traffic-protein-EboE
MRFRHPDGSIIHLAYCTNVHPAETLDGVLAQLRDHCEPVRKRLGRDRIGIGLWLAKDAAHALVTDPAALRGLRTELDRRGLEVVTLNGFPYEGFGSAEVKYRVYKPDWADPERLEHTSSLARILAQLLPDDVTEGTISTLPLAWRTAFGPARAQAAHTALGSLAQRLDALAELTGRSIRIGLEPEPGCIVETTGDAIEPLTEVGHSRIGVCVDTCHLATSFEDPHTALGALAAAGIPVVKTQLSAALHAEHPHLPEVRAALAAFDEPRFLHQTRTVPRGPARPATAGAPDAVLRGTDDLGEALAPGALPDTAPWRSHFHVPLHAAPAPPLTSTLSVLKDTLALLVGGPHPRTRHLEVETYTWQALPPELRPRARPQLVDGIAAELTLARDLLTDLGLKELP
>NZ_CP030771.1|WP_138962662.1|7647762_7649163_+|alkaline-phosphatase-family-protein
MTPPVPGRPNPLLVLDVVGLTPHLLAHMPHLAALGTSGSRAPLGTVLPAVTCAAQSTFLTGTTPAEHGIVGNGWYFRELGDVLLWRQHNGLVAGDKLWDAARRAHPGYTVANICWWYAMGADTDITVTPRPVYYADGRKEPDCYTRPPALHDELTEKFGTFPLFHFWGPGADIVSSRWIVDATRHIIDTRRPDLALCYLPHLDYDLQRYGPDDPRAHRAAADLDAVIAPLLADAKAEGRTVVALSEYGITRVSRPVDINRALRRAGLLDVHTQDGMEYLDPMASRAFAVADHQIAHVYVRRPEDLEATRAALDGLDGIDQLLDDEGKKAHHLDHPRSGELVAVAEADAWFTYYYWLDDARAPDFAQLVEIHRKPGYDPVELFMDPEDPYVRLKAAGALARKKLGMRYRMAVVPLDPSPIRGSHGRLPTSEDPDSGPLILCSTPRAVAGRVAATDVKSLLLQLAGLD
>NZ_CP030771.1|WP_138962663.1|7649364_7650465_+|TIM-barrel-protein
MSRKPTPDDPELAHRLSRRGMLGVAAGATAAALAGTAAAAGPASAATAGPASAATTPTTDAAQPSGKGRGRPVLPPGRLGVQLYSLRDKVSSLGFAAVFAELERYGYDEVEFAGYAQGSAGAITLARLKRLVRDHGLTAIGSHVGYYSDGDPNAYTFAQNLTKVLDDAEALGLKHIGTASGPFRYGTTVDAWKRAAEDFNTYGEAARARGMKFYQHNHAEEFSFATNKPSVRLYDVLLAETDPDLVYLEMDIYWAHSARFRFGKQVDGTPRPFDPIDYVLRRPHRYPLFHVKDGIRDDSTRDGYRMVDVGDGDIDYKKFLSKVTARTQGGRRYHHWQVEHDSPSDSFAFARKSSAHLHALRERCGD
>NZ_CP030771.1|WP_138967285.1|7650648_7651899_-|MFS-transporter
MVALPWVAMIAISVFEYAYGAAEDTLSDAHHWTSSNTFWVLSVWIFFQAGVSFPAGKLREKGILTSRAAMLTGSVLSMLGFVSLSHAPNVVAAMVGFGLLGGVGSGLIYSTSVNMVGKWYPERRGGKTGFVNGGFAYGAVPFIFLFSYGFDTSNYRTVLDLVGFYVLAVTLVAGLFFKDPPKNWWPESVDPLRSVTGTRTAVALAKNPPAVAQFTPGEALRTGVVPLMWVCMLCCAGVSIFGISFQVPFAKEMGFGPMIAASSMGVMSVINGTGRGVVGWLSDLLGRRPTLTYVCLALSVAQFGVLWAGAIRNEPLFLVFAFLSGFAGGAFYPLFAALVPDYFGENNNASNYGMVYSAKLVSGLFGGGVGAMVVHSWGYIGAYTTAGAVSLLAAGLSLLLRQPSSPRARGELARSG
>NZ_CP030771.1|WP_138962664.1|7652182_7653571_-|MFS-transporter
MTTTDLTAPVPFREVTDRNGRLYRIGETDVDIMGRPRWTMVLFPWMGMLGISSSEYAFTSAEDTLHDAHLWSGGHIFWLMGVWVFFQAAVAFPAGQLRESGRLPARYAMLLGAFGTVCGYLSLAYAPHVTVAYVGFGMFSGIGAGLVYATCVNMVGKWYPERKGGKTGLVNGGFAYGSVPFVFLFTSYMDVSNYHGVLIFVGAVCASVVAFAGWFFKDPPKGWWPPHVDPLKVSADPRVRRALEKNPPAVKQYTPREAAHTPVLWLMWFCLLCTAGINIFGIAFQVPFGKDMGFAGGVVVTAMSLKAIVNGTGRGVIGWISDRYGRRSTLVIVCLVLGVAQFGALASGSMGSMPFFLFCSMVSGFGGGAIFPLFAAMTADHFGENNNATNYGVVYSSKLISGLVGSGLGAVVVDAWDYEGAFVIAGCIGICSAVLALFLKAPGRPCARRVVPNPHPLGEEMA
>NZ_CP030771.1|WP_138962665.1|7653705_7655862_-|acetate--CoA-ligase-family-protein
MPADDRSERVRALLDSVRAEGRTSLTAPEGKILADAYGIAVPGEELARDVDEAVAHAARFDGPVVLKIVSPDILHKTEAGGVVVGVEGAEDVRAAFHRIVDNARAHAPTARLDGVQVQELLPSGADAREVIVGAVTDPTFGKVVAFGLGGVLVEVLKDVTFRLAPVDVEEAASMLDSIAAAEILRGVRGAQPVDRGALAEQIRRVSQLVTDFPEIAEVDLNPVIATPRGALAADVRVILGDRAPEERHTYTRAEMLASMRRLMQPRSVAVIGASNEPGKIGNSVMRNLIDGGFAGEIHPVNPRADDILGRKAYKSVTDVPGEVDVAVFAIPAAFVAKALEDVGRKGIPNAVLIPSGFAETGEQALQDEIVAIGRRHGVRLLGPNIYGYYSTWQDLCATFCTPYDVKGGVALTSQSGGIGMAILGFARTTKTGVSAIVGLGNKSDLDEDDLLTWFGEDPRTQCIAMHLEDLKDGRAFVEAARATVPKKPVVVLKAGRTAAGARAAGSHTGALAGDDAVYDDVLRQAGVIRAPGLNEMLEYARALPVLPTPRGDNVVIITGAGGSGVLLSDAVTDNGLRLMEIPPDLDAAFRAFIPPFGAAGNPVDITGGEPPSTYEATIRLGLEDPRVHALVLGYWHTIVTPPMVFAELTARVVAEFRARGVDKPVVASLAGDVEVEEASQYLFERGVVAYPYTTERPVEVLGAKYRWARAAGLLGGGR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_17

7746343-7746407

Orphan

Consensus_repeat	Method
GCGCCGTGGCTGCCCACCGCGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_17

>merge|NZ_CP030771|17|7746343-7746407|CRISPRCasFinder
GCGCCGTGGCTGCCCACCGCGGGCCCGGCGGACCTGGGGCCCACGCCTTGGCCTCCCACTGCGGG

>NZ_CP030771|17|15|7746343-7746407|CRISPRCasFinder
GCGCCGTGGCTGCCCACCGCGGG	CCCGGCGGACCTGGGGCCC
ACGCCTTGGCCTCCCACTGCGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_030668194.1\|7739896_7740157_+\|WhiB-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376791
NZ_CP030771.1\|WP_138962730.1\|7750453_7752742_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223256
NZ_CP030771.1\|WP_138962729.1\|7749523_7750411_+\|DUF4394-domain-containing-protein	unknown	unknown	gnl\|CDD\|373019
NZ_CP030771.1\|WP_138962724.1\|7738207_7739431_-\|sugar-hydrolase	unknown	unknown	gnl\|CDD\|185759
NZ_CP030771.1\|WP_171075902.1\|7757976_7758129_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138962731.1\|7752752_7754417_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223562
NZ_CP030771.1\|WP_138962723.1\|7736982_7738140_+\|acyltransferase-family-protein	unknown	unknown	gnl\|CDD\|224748
NZ_CP030771.1\|WP_138962725.1\|7740196_7742668_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_171075901.1\|7730209_7732756_-\|ThuA-domain-containing-protein	unknown	unknown	gnl\|CDD\|377643
NZ_CP030771.1\|WP_138962734.1\|7757617_7757917_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|367663
NZ_CP030771.1\|WP_138967298.1\|7733059_7734004_+\|multicopper-oxidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|259991
NZ_CP030771.1\|WP_138962721.1\|7734725_7735802_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP030771.1\|WP_138962732.1\|7754797_7755631_+\|isocitrate-lyase/phosphoenolpyruvate-mutase-family-protein	unknown	unknown	gnl\|CDD\|379346
NZ_CP030771.1\|WP_138962728.1\|7747975_7749244_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379258
NZ_CP030771.1\|WP_138962720.1\|7734029_7734548_-\|RICIN-domain-containing-protein	unknown	unknown	gnl\|CDD\|366226
NZ_CP030771.1\|WP_138962727.1\|7746860_7747847_-\|acyl-ACP-desaturase	unknown	unknown	gnl\|CDD\|153109
NZ_CP030771.1\|WP_138967301.1\|7756451_7757621_+\|oxidoreductase	unknown	unknown	gnl\|CDD\|226855
NZ_CP030771.1\|WP_138962722.1\|7735922_7736684_+\|NAD(P)H-binding-protein	unknown	unknown	gnl\|CDD\|187554
NZ_CP030771.1\|WP_138962733.1\|7755716_7756133_-\|SsgA-family-sporulation/cell-division-regulator	unknown	unknown	gnl\|CDD\|377399
NZ_CP030771.1\|WP_138962726.1\|7742889_7746312_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_030668194.1\|7739896_7740157_+\|WhiB-family-transcriptional-regulator	gnl\|CDD\|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	5.74726e-25
NZ_CP030771.1\|WP_138962730.1\|7750453_7752742_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223256	COG0178, UvrA, Excinuclease ATPase subunit [DNA replication, recombination, and repair].	0
NZ_CP030771.1\|WP_138962729.1\|7749523_7750411_+\|DUF4394-domain-containing-protein	gnl\|CDD\|373019	pfam14339, DUF4394, Domain of unknown function (DUF4394). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 262 and 476 amino acids in length.	1.59095e-76
NZ_CP030771.1\|WP_138962724.1\|7738207_7739431_-\|sugar-hydrolase	gnl\|CDD\|185759	cd09220, GH64-GluB-like, glycoside hydrolase family 64: beta-1,3-glucanase B (GluB)-like. This subfamily is represented by GluB, beta-1,3-glucanase B , from Lysobacter enzymogenes Strain N4-7 and related bacterial and ascomycete proteins. GluB is a member of the glycoside hydrolase family 64 (GH64) involved in the cleavage of long-chain polysaccharide beta-1,3-glucans, into specific pentasaccharide oligomers. Among bacteria, many beta-1,3-glucanases are implicated in fungal cell wall degradation. GluB possesses the conserved Glu and Asp residues required to cleave substrate beta-1,3-glucans. Recombinant GluB demonstrated higher relative activity toward the branched-chain beta-1,3 glucan substrate zymosan A than toward linear beta-1,3 glucan substrates. Based on the structure of laminaripentaose-producing, beta-1,3-glucanase (LPHase) of Streptomyces matensis, which belongs to the same family as GluB but to a different subfamily, this cd is a two-domain model. Sometimes these two domains are found associated with other domains such as in the Catenulispora acidiphila DSM 44928 carbohydrate binding family 6 protein in which they are positioned N-terminal of a carbohydrate binding module, family 6 (CBM_6) domain.	1.43705e-173
NZ_CP030771.1\|WP_138962731.1\|7752752_7754417_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	2.57733e-121
NZ_CP030771.1\|WP_138962728.1\|7747975_7749244_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	8.22611e-12
NZ_CP030771.1\|WP_171075901.1\|7730209_7732756_-\|ThuA-domain-containing-protein	gnl\|CDD\|377643	pfam06283, ThuA, Trehalose utilisation. This family consists of several bacterial ThuA like proteins. ThuA appears to be involved in utilisation of trehalose. The thuA and thuB genes form part of the trehalose/sucrose transport operon thuEFGKAB, which is located on the pSymB megaplasmid. The thuA and thuB genes are induced in vitro by trehalose but not by sucrose and the extent of its induction depends on the concentration of trehalose available in the medium.	5.78428e-75
NZ_CP030771.1\|WP_138962734.1\|7757617_7757917_-\|hypothetical-protein	gnl\|CDD\|367663	pfam03795, YCII, YCII-related domain. The majority of proteins in this family consist of a single copy of this domain, though it is also found as a repeat. A strongly conserved histidine and a aspartate suggest that the domain has an enzymatic function. This family also now includes the family formerly known as the DGPF domain (COG3795). Although its function is unknown it is found fused to a sigma-70 factor family domain in CC_1329. Suggesting that this domain plays a role in transcription initiation (Bateman A per. obs.). This domain is named after the most conserved motif in the alignment.	4.10739e-16
NZ_CP030771.1\|WP_138967298.1\|7733059_7734004_+\|multicopper-oxidase-domain-containing-protein	gnl\|CDD\|259991	cd14449, CuRO_1_2DMCO_NIR_like_2, The cupredoxin domain 1 of a two-domain laccase related to nitrite reductase. The two-domain laccase (small laccase) in this family differs significantly from all laccases. It resembles the two domain nitrite reductase in both sequence and structure. It consists of two cupredoxin domains and forms trimers, and hence resembles the quaternary structure of nitrite reductases more than that of large laccases. There are three trinuclear copper clusters in the enzyme localized between domains 1 and 2 of each pair of neighbor chains. Laccase is a blue multi-copper enzyme that catalyzes the oxidation of a variety of organic substrates coupled to the reduction of molecular oxygen to water. It displays broad substrate specificity, catalyzing the oxidation of a wide variety of aromatic, notably phenolic, and inorganic substances. Laccase has been implicated in a wide spectrum of biological activities. This subfamily has lost the type 1 (T1) copper binding site in domain 1 that is present in other two-domain laccases.	4.17925e-65
NZ_CP030771.1\|WP_138962721.1\|7734725_7735802_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	7.89779e-92
NZ_CP030771.1\|WP_138962732.1\|7754797_7755631_+\|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.	2.03344e-87
NZ_CP030771.1\|WP_138962720.1\|7734029_7734548_-\|RICIN-domain-containing-protein	gnl\|CDD\|366226	pfam00652, Ricin_B_lectin, Ricin-type beta-trefoil lectin domain.	8.11019e-08
NZ_CP030771.1\|WP_138962727.1\|7746860_7747847_-\|acyl-ACP-desaturase	gnl\|CDD\|153109	cd01050, Acyl_ACP_Desat, Acyl ACP desaturase, ferritin-like diiron-binding domain. Acyl-Acyl Carrier Protein Desaturase (Acyl_ACP_Desat) is a mu-oxo-bridged diiron-carboxylate enzyme, which belongs to a broad superfamily of ferritin-like proteins and catalyzes the NADPH and O2-dependent formation of a cis-double bond in acyl-ACPs. Acyl-ACP desaturases are found in higher plants and a few bacterial species (Mycobacterium tuberculosis, M. leprae, M. avium and Streptomyces avermitilis, S. coelicolor). In plants, Acyl-ACP desaturase is a plastid-localized, covalently ACP linked, soluble desaturase that introduces the first double bound into saturated fatty acids, resulting in the corresponding monounsaturated fatty acid. Members of this class of soluble desaturases are specific for a particular substrate chain length and introduce the double bond between specific carbon atoms. For example, delta 9 stearoyl-ACP is specific for stearic acid and introduces a double bond between carbon 9 and 10 to yield oleic acid in the ACP-bound form. The enzymatic reaction requires molecular oxygen, NAD(P)H, NAD(P)H ferredoxin oxido-reductase and ferredoxin. The enzyme is active in the homodimeric form; the monomer consists mainly of alpha-helices with the catalytic diiron center buried within a four-helix bundle. Integral membrane fatty acid desaturases that introduce double bonds into fatty acid chains, acyl-CoA desaturases of animals, yeasts, and fungi, and acyl-lipid desaturases of cyanobacteria and higher plants, are distinct from soluble acyl-ACP desaturases, lack diiron centers, and are not included in this CD.	2.19381e-129
NZ_CP030771.1\|WP_138967301.1\|7756451_7757621_+\|oxidoreductase	gnl\|CDD\|226855	COG4447, COG4447, Uncharacterized protein related to plant photosystem II stability/assembly factor [General function prediction only].	4.06118e-15
NZ_CP030771.1\|WP_138962723.1\|7736982_7738140_+\|acyltransferase-family-protein	gnl\|CDD\|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	1.94802e-31
NZ_CP030771.1\|WP_138962733.1\|7755716_7756133_-\|SsgA-family-sporulation/cell-division-regulator	gnl\|CDD\|377399	pfam04686, SsgA, Streptomyces sporulation and cell division protein, SsgA. The precise function of SsgA is unknown. It has been found to be essential for spore formation, and to stimulate cell division.	4.28193e-34
NZ_CP030771.1\|WP_138962722.1\|7735922_7736684_+\|NAD(P)H-binding-protein	gnl\|CDD\|187554	cd05243, SDR_a5, atypical (a) SDRs, subgroup 5. This subgroup contains atypical SDRs, some of which are identified as putative NAD(P)-dependent epimerases, one as a putative NAD-dependent epimerase/dehydratase. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine-rich NAD(P)-binding motif that is very similar to the extended SDRs, GXXGXXG, and binds NADP. Generally, this subgroup has poor conservation of the active site tetrad; however, individual sequences do contain matches to the YXXXK active site motif, the upstream Ser, and there is a highly conserved Asp in place of the usual active site Asn throughout the subgroup. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	5.05857e-28

>NZ_CP030771.1|WP_138962726.1|7742889_7746312_+|hypothetical-protein
MARPDPAAAAARLLADLDPLPYPERMRRLARVGQARRGEVREWLPALEGGAAAPGPGRRWGRARRERDGTDRFVPGRAHERGVAVLLASVTGDTAWIAARLADPDAFVRGHALRAADAVGVPDAAFEAALTDAPRAVRRALLRALAAGRRTALADRLVDGVRRDWGDAEAARLLPGCSDDVVARLLPEVLYAVRALTALAKRHHGVLLDVVTRELAAAPDVLRDACWERCGAALAAGAEHDPLRALDLLERYAPSSFPSQLLPRVGVFAAVAPDRVLRLLAGEWGAVLRRSGRLTRSVLRRLARHGGPGLTAYARSVADDSAALTQLLAAHPPAARPALYAAAVEGRGPGAATVDSGLWDVLPRRAAADEARRVAARARAEGAYWTTVLAAESHLPCAEVRERLVAATRRPVADDRAEAWPFLVRNAARSRDAAEVSLVVRDMAERLANEQDPVRAEALYALSTVRPALFDPGAVERLDRIAADAVAARDCSYDTRDALGSLALAVLREHAGNPRTELVGWGLRTLTLLTGSTGRADFGRLDRALRRGQEHAVYEALRPWIEAGAEKADYGLAFALARAVGRRARGMAALQDLLWRAILRGDNPTAATAIGLWLDAAPTPAERDDRVARVLAREPSAAALDPVRTVLTHRRTDLLDPLLGARPPYGRFLTPGSAWTLPAAPGVVRRWTARQQEAWARQLGAAVADEKLPLAERAAALARGAAVPGAGADLARQWSAAADVRLGEAGLAALAHTDRPGDAVPALLAHAGDERARVAVYAAGRASRYAAPSLLAGPLREVLTGPGVKVTSRKEAARLVAARLPAATAASLLREAYRAPGAHPDVRAACVASCGGLLGEAPAGELLADAARGEPASRFAVLRMSPLDVAPAHRERYANLVCDVGAADDAEAAVLAFGVLPRWAPWSAGAAEVLGAACADLARGRAVWQAAADGLVTAAVTALRGDEALCGALASLAAVPGEAGLGARRRVEHVVARLVVRQGAAGRSVARRAGELLTSYEDFRPQAVRLLVAAVEVGGARVGPDLERVAELHEGRPVLAGATARALAERLAGVDASLAGAALLPVARALAAGPGTARPLFAVSLAQTLGSRTGWPAPWRDLLTDLRHHALPDTRDAALAVTLP
>NZ_CP030771.1|WP_138962725.1|7740196_7742668_-|hypothetical-protein
MAQTHEWMFYEVMWRGWADRARVPHPVPWWAQAAFRRWSDDFDQGTYASKEAAFASNALYRYWHMVGVKDHRQESLVGQAGEIEPVYDKYCLAFFLYDPAAGAVRLPQLAGGGTVEQRVEAPHLPVVVTEFRSADGVAYAQRTFATAVGARRRDLAVTRLAVRSQDGRPREGWLCAAVLPAGPSGFQRHDRRGEQLTDRRLTFLRYLPDEARVETNSGWGPVFDAPPEHYGVYGNPDFTTDPGAYLVRSPFHDLVTGGKLNAALQAQDQVAGLCSAAFAWPFRVADDEVFALDVRLPVDLYSGADDLAELRATPAAELEQANRAFWAAKLLGQGVRPELPEPVAHLADRFRQCRAQLLVLSDHGEIHPGPTVYDSFWIRDSSVEATACSLVGDTALAERQLGTHYPLRFNRGTGRIGPCAEYGFYGGPHEKDDREWDSNGQALWAIGRFDRTRGRDAAFGAKLYAPYVVDAARWLRDNRDAYGLLHSGWSAEHLGERDKPHYWDDLWGLAGLYEAARLAERLGTPEAAELWAAFDDLKRATAASIRWVLAEQRRRGDWETYIPTGPGDVGRLDSTMIGAAAYFHPLRLHMGDKLGGDVDRAARWTLDTMYARFVTGGFRHEAAWNAYGPYLTMQLAHAYLLAGDPARMDALLGWTVAAASPRAEGRAVALGAWNEQHAFPIASDYGEVPYRHWYMGDIPHGWAAAEYLLLVRDILFFEADEDRDPHVYVAPGVRPHWVPDGAAVAVGAAPTLFGAPFGYRLAHDAGERTVTVDVTDAPQGVRYVYPCRFGPVRAATADGRALPVAGDDVHVPAGTARFTVTYG
>NZ_CP030771.1|WP_030668194.1|7739896_7740157_+|WhiB-family-transcriptional-regulator
MHIDTTVTEAELAWQEQALCAQTGPDFFFPDPGSSVREAKRICRLCDMRSACLAYALDNDERFGVWGGLSEKERQSLRRERVSRTA
>NZ_CP030771.1|WP_138962724.1|7738207_7739431_-|sugar-hydrolase
MISRRVFLTSSAATAGALTYPVRGGALSPRAEAAPATCELVLRNKSLPGQVRAYVTGHEPGTGRWLLLRPDGGVHRPESPPAPHTPLAVDCAIPLGAAGSAPRILTLPQMYGARVYFVRDDRLDFLLNPGPALVEPAFANPADPHYGRTWSFCEFTFNSTQLYANISYVDLVTALPIGLTLEGDATHTVAPLPGGAVDRIAADLVAQAGRDGQPWDRLVVRGGGRVVRVVSPQNVMAPYFDRPDQMPFRDLFTAYADQVWEKYRSTDLRIDLQGGRGVRVGRVSGNTLTFAGGHTFTKPSSKDVFTCNHGPFANNPADPDDKKALLARLAAGFNRGLMLTHPTQPNGTTAADYYRGPVTNHWARVVHANSPIGYAFPYDDVRPDGQPDVSGAAHDNNPRRFTVSVGA
>NZ_CP030771.1|WP_138962723.1|7736982_7738140_+|acyltransferase-family-protein
MATDAVRPKLSRLPSLSGMRFIAALPVFAFHGTSGMNFLRGDTGEFFTDLFKDAGTPSVSFFFVLSGFILTWSARPRDTVPGFWRRRMIKVYPNHLLAFAATVVIMLLASDPFEAKKFFTSLFLVQSWVPELPVLTGMNPVAWSLSCEVLFYLSFPLLLPLVRRLSVRGLWVAAGVLVAVPWLAVVFAQNVIDGTPLLPGQPLTHEQLWFVYFFPVTRMAEFVLGIVVARLVLGGSVPRIGLVPAALFALGGYLLNAQVPYLYSVGGTAAFWVAPLVVAGATADVRGTRSAMRGRVMVKLGELSFAFYLVHVMFLVSAQRWLVQDMSDGAALATFIGCFAGSLAVAYALFTWVESPLVRKFGSAPRPKPTLAPAPTAEPLTAAKD
>NZ_CP030771.1|WP_138962722.1|7735922_7736684_+|NAD(P)H-binding-protein
MAASILVTGGTGTLGRLVVPLLRTAGHEVRVLSRHAHAPGDGITYVTGDLVKGEGVAEAVAGVDTVLHLAGGPKGDAEAAGHLVRAARAAGVRHLVYISVIGADRVPLGWFRAKLQAERAVAESGIPWTTLRAAQFHDLVLTMAEKMAKLPVLPVPGGLRFQPVDAREVAARLAELTLGEPAGLVADLAGPKVYGMGELNRGYLKARGKHRLLMPVRMPGKAGRAYRAGENLTLDGASVGRRTWEEFLAERVR
>NZ_CP030771.1|WP_138962721.1|7734725_7735802_+|substrate-binding-domain-containing-protein
MSEAGARPTLEAVAARAGVSRATVSRVVNGEAGVREVLAVKVRRAVDELGYVPNRAARSLVTRRYDAVAVVIAEPETRVFADPFFALQLRGISKELTAHDVQLVLLLTEGRADHARVGRYLSGGHVDGALVFSLHLDDPLPVIINGAGVPTVFGGRPGWTGGEDSVRYVDCDNRGGARTAVRHLAGLGRTRIAHITGALDQTSAADRLDGFRDVLPAGDARLVAEGDFTPAGGERAMRHLLDRCPDVDAVFAANDLSAAGALRVLRAAGRRVPDDVAVVGFDDMLPVAEQADPPLTTVRQDIEEMGRLMAAMLLRGQDRCPAPDDGRVRPRERPRGADDVGHAASVVLPTELVRRESA
>NZ_CP030771.1|WP_138962720.1|7734029_7734548_-|RICIN-domain-containing-protein
MKVTRRLTALTAALVTAASGALLTGAAPAGAAEPDPGSLFRNTGNGLCMSTADDPANAFQGTATFAPCDLGDPRQRWRLNLANQPAWQISSVSTGKCLADVAGWGLAWLGTCDANDVDQFWHFNGNQAGDLFWVSHDDGKLLSTPYREGTSYVTVRHDLDPKDARYKWSLLR
>NZ_CP030771.1|WP_138967298.1|7733059_7734004_+|multicopper-oxidase-domain-containing-protein
MSAMAPEAVPAEEPPRRAPAGGEVRRVTMYAEKLPDGQLGYGLERGKASVPGPLIELNEGDTLHVDFENTTDVAVSLHVHGMDYEISSDGTKHTRSDVAPGKRRTYTWRTHVPGRRKDGTWRPGTAGYWHYHDHVVGTDHGTGGLRKGLYGAVIVRREGDVLPDKTCVIVFNDMMINNRPAHSGPDFEATVGDRVEFVSITHGEYYHTFHIHGHRWADNRTGMLTGPDDPSQILDDKITGPGDSFGFQVIAGEGVGAGAWMYHCHVQSHSDMGMVGLFLVKKPDGSIPEYEPHHPRAGAGAGAGAEPESGGAHH
>NZ_CP030771.1|WP_171075901.1|7730209_7732756_-|ThuA-domain-containing-protein
MRLTPRQQPLTTREFGRSRYRASRRSWAAAMAAGVLAAGVLSGPAASARPFPEPPGDAEAMKTTMSRALPAPPGGANVRVLAFYGSAAPGDESPVVDAAIAAIEKIGRSGPTAQRFTVTATDDPAVFTDARRLGTFNAVAFVTGGGDVLDPEQEAGLEAYMEAGGGFLGLHDAARAEPYSSWFTGLVGARPKDESPAAVQRATVEVGDRQSPATKDLPLEWKRPDQWLNWETNPSGTVHTVARVRETTYKPGAGANGWDHPVSWCRDYDGGRSFYTGMGGTADAYDETDFRAHLRGALLWTTRLVRADCKAAITDNYRAERLTQPNKPGQNDQIGEPHGLVTAPDGTVFYIGRGGADSSRPVVTDWNDPDVGKGRGEIHVYDPRTKQVTLAGAVSVFGNKGGGGELTKNEEGLLGIELDPRFESNGWVYLHYTPHARINRETHMGERYVSRFTYDKASGKLAMDSEKVLLKWPVQVHSCCHAGGGMAWDSKGNLYIATGDNNSSGSSDGYSGNNPQPNFMGVSFADARRTAGNTHNLNGKILRIHPEPDGTYTLPEGNLFTGKEPDEGGGKTRGEIYVMGVRNPARISIDKKTDTLYAGWVGPDAGQPSTTWGPAKYDTFAAITHASNRGWPYCMGNNQPYRDRNLPDPGKPLGWYDCKNLRNESPNNDGLVKIPPAEPNTIWYSPQGGGIDYPRDANGVPSYRTEEQKQLLPWLKGGGQATMNGPVYRYDPASTSADKWPAYWDGKWFVGDFYDGDQPRHAVLTDPRTVGTGGLPVHAESLRKIIPVGNDRIKNLMDWKFAPDGSLYVLDYGRGFFTSDARSALWRVTYTGGGATPAAGDLARKAGR
>NZ_CP030771.1|WP_138962727.1|7746860_7747847_-|acyl-ACP-desaturase
MTLTSPHLGSPDTWTDARLLYALEEVVEQELNRHLKVAKDWMPHEYVPFSDARNFPGQFEDGEAWALGQSPVTDVGRIALVVNLLTEDNLPSYHHEIATLFGRDGAWGTWVHRWTAEEGRHGIVMRDYLLASRAVDPDELERFRMAHMSEGFESDNRHSMLHSVAYVAFQELATRISHRNTGHQSGDPVCDRMLARIATDENLHMVFYRNLLRAAFDLAPDATMMAVRDVVVGFRMPGHGIPGFERAAAKMAIGGVYNLRIHHDDVLQPVLRFLKIMSIPGLGPEGARAQEELGLFLDGLDGEARRFDERLAARQARIDARAGAKAQA
>NZ_CP030771.1|WP_138962728.1|7747975_7749244_-|helix-turn-helix-domain-containing-protein
MGSLFAELARQAANSARREVETYTREIPEFASLDADTRARAETLEYAVWLRRRTIELSPDNTALTASDLADIASMGEVRGGSGMSLESRQEVLRLHTALMLREINEAVEAQRGGGAEELLRMMSWFAPQGERGIAAYCQGFVTALSRRLPYVEQVALLARTLLAHDPLAAELASAVGMELPGSFAVTVIRVPHGAGGHHGPEREVEALVKTHRVPMVWCPAGDGGGELIALIPDTDAEADINADAPARAHTVTGRAPDHLPGLVFDSVPGLALDLVRDFAGAVGRPCAAGTATAPLAELADALEGARRISRATPLRRAPARLRPHTAADVFVELAVVDVPFVDSWLATVARHLEPGPDLVLTLDAYYHHDMDRGATAAALNVHPRTLDYRLRRVRDLTGLAPGSTRGVRVLSAAVTRHLAVR
>NZ_CP030771.1|WP_138962729.1|7749523_7750411_+|DUF4394-domain-containing-protein
MKIRSRTHGRRRFAAAVALLTASTALVMGAPGTGSAAPAATPSLQAFGISGDGLLMAAFKTDNPRQLDWVREITGLKGDQKVVGIDFRVQDGQLYGVGDKGGIYTFKWPPEVPEPTATKVSQLQFDLLGTNFGVDFNPAADRLRVISDGAQNLRHNLNTHTTDEDVALTTPPITGWTRGVSAAAYTNNDLNGATGTLLFDVDTKLDQLVVQAPANNGTLSSVGSLGVDAGPNAGLDIYSTLSGGKTVSNAGFAILGPASGTGNPSLYNVNLFTGATDVIGRFPVNITDIAIYPSK
>NZ_CP030771.1|WP_138962730.1|7750453_7752742_-|ATP-binding-cassette-domain-containing-protein
MHAATDHGHIVLTGARENNLKEVSLRIPKGRLTVFTGVSGSGKSSVVFDTVAVESQRQLNETFTWFVRNRLPKYERPQADAIEDLAPAIVVDQKPIGGHSRSTVGTMTDIYSVMRVLFSRHGTPGAGPATAYSFNDPSGMCPECAGLGRTVRPDYDRILDPARSLADGAVRFPPFAAGTWQGQTYTNSPDLDPHKPLGDFTAEERHFLLRGHPDSGKVSVDNTGGARAIDFEGLADRFERLYLHRDLSALSQKTRDLVQGFLVEGRCPACAGARLNPAALASRINGLNIADCARMEVTDLVAELGRVQGPVAGPVARAAVAALERVEAIGLGYLSLDRETSTLSGGEGQRLKMVRHLGSSLTGMTYIFDEPSVGLHPRDVGRLGDLLLRLRDKGNTVLVVEHDPDVIAIADHVVDMGPGAGTHGGRVVFEGTPHELRAADTPTGRALRRPAGVREHPREPVGSAWIKGADLHNLKDVSVRVPLGVLTAVTGVAGSGKSTLVTGAFTAQHPDAVVVEQSAIGISGRSTPATYLGIMDRVRALFARHTGTEPGLFSFNSSGACERCQGRGISYSDLAFMDPVTTICEECAGRRFKQEVLRLTVGGRSIADVLDMTAEQALAFLADFPDPAVRRRLGALRDVGLTYLTLGQPLSTLSGGERQRIKLATQLHRTGTTYVLDEPTTGLHMADVDGLLALLDRLVDAGNTVLVVEHNLDVVRHADWVIDLGPDGGKHGGRVVFEGTPRELLAAEGSFTAEHLRRSVAA
>NZ_CP030771.1|WP_138962731.1|7752752_7754417_-|ATP-binding-cassette-domain-containing-protein
MSTVPTPSITCTSLSFAWPDGTSVFDGLQAAFGPGRTGLIGRNGSGKSTLLKLVAGELAPAEGTVRTAEDVGYLPQNITLDTALRVDEVLGIAGTRAALHAIEAGDVREEHFTAVGDDWDVEERARATLDQLGLAHIGLDRTTGEVSGGESVLLRLAALLLRGPGVLLLDEPTNNLDLYARRRLYAAVDAWSGVLVVVSHDRELLDRVDHIADLHEGEVTWYGGNFSAYEQALAVEQEAAERMVRVAEADLRKQKRELADAQVKLARRKRYGQKMWDQKREPKVVMGNRKRAAQESAGKHRILHEEKLAEAKERLDDAVEAVRDDDDIRVDLPHTAVPPGRTVLTLSNLTLRYGARVRGEFELRGPERVALVGRNGAGKTTLLRTIGGDLAPVGGEALAQVPLRFLPQRLDVLDDDLTVAENVARQAPDATNNRVRARLARFLFRGAKADQQAATLSGGERFRAALAALMLADPAPQLLLLDEPTNNLDMASVRQLSSALEAYEGALIVASHDVPFLESIGITRWLLLDGEIKEITGKHREKMENRTGAVGYPE
>NZ_CP030771.1|WP_138962732.1|7754797_7755631_+|isocitrate-lyase/phosphoenolpyruvate-mutase-family-protein
MTHVNDLATAFRDLHVPGSPLVLPNAWDAASARLVETAGAAAVATTSAGLAWALGAGDGDRLTRDQALGAVARIVDTVSVPVTADVESGYAEDAEGVADTVRAVLAAGAVGVNIEDARHAAGDPLRPVAEQAERIAAARGAADAAGVPLFVNARVDTYLRGAGEGAAERLALTLERAAAFLDAGADGVFVPGVVDPETVEALVAKVDGPLNVMAGPGAPPVARLAALGVARVSVGSGIAQAAHALVRGAARELLTEGTYGSLTGGLDFGEADALFSR
>NZ_CP030771.1|WP_138962733.1|7755716_7756133_-|SsgA-family-sporulation/cell-division-regulator
MSTVIEQAVEARLVAAAPRMPTIPATLHYDQRDPFAVRMSFPAPATLEGVEVHWTFARDLLSQGVENTVGDGDVRVRPYGYERTVLEFHAPEGTAIVHVRTGDLRRFLHRTMVLVPAGQEHRHVDLDQDLADLMRDAC
>NZ_CP030771.1|WP_138967301.1|7756451_7757621_+|oxidoreductase
MGVALGAVALAAASLVAPGAAGAVDRAGAGAEGVAGARGGAGAEAGSAGAGAEAGGAGAAGHRGGSPRWDLKPTGTDARFRGLAAVSRSTAWAAGSKGTVLRTADGGAHWRNVSPPGASGLEFRDVEAFDGRRAVALAIGEGEASRLYRTADGGKTWTEAFRNAEPKAFYDCMTFFDRRHGLALSDPVDGAYRILSTADGGRSWKVLPATGMPAAQEGESAFAASGQCLVSAGPRDVWLATGGAARARVLHSADRGLTWTATDAPIPAGDPARGVFGLAFRDRAHGLAVGGDYRAGEASPRAAAVTRDGGRTWRPAARPVPAYRSGVAWLPYSRTTALAVGPTGTDLTTDAGRSWRTVDEGSYDTVDCAPDLGCWAAGEKGRVARLERR
>NZ_CP030771.1|WP_138962734.1|7757617_7757917_-|hypothetical-protein
MFVMELTYTAPVDRVDALLAEHVAWLDAQYAAGVFLASGRKNPRDGGVILAVGDSRAEIEGLAALDPFVTGGVCEYRITEFLATKTAPALADHRQRLPA
>NZ_CP030771.1|WP_171075902.1|7757976_7758129_-|hypothetical-protein
MPAIPAESRRRATKCGSAIVLMTFVLLSTTAICMPSDVKSSTRPPARLNR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP030771_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP030771_18

7984217-7984387

Orphan

Consensus_repeat	Method
CATCGCGCTGCGCGCTCGTCCTCAAGCGCCGGACGGGCTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP030771_18

>merge|NZ_CP030771|18|7984217-7984387|CRISPRCasFinder
GATCGGCCTTCGGCCTCGTCCTCAGGCGCCGGACGGGCTTGACCATCGCGCTGCGCGCTCGTCCTCAAGCGCCGGACGGGCTGTATGGCTGTGGTGCGGCTCGTCCTGCGGGCGTCGCGCGGGTTCGTGATCATCGCGCTGCGCGCTCGTCCTCAGGCGCCGGACGGGCTG

>NZ_CP030771|18|16|7984217-7984387|CRISPRCasFinder
GATCGGCCTTCGGCCTCGTCCTCAGGCGCCGGACGGGCTT	GACCATCGCGCTGCGCGCTCGTCCTCAAGCGCCGGACGGGCTGTATGGCTGTGGTGCGGCTCGTCCTGCGGGCGTCGCGCGGGTTCGTGAT
CATCGCGCTGCGCGCTCGTCCTCAGGCGCCGGACGGGCTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP030771.1\|WP_138962996.1\|7988163_7989093_+\|branched-chain-amino-acid-transaminase	unknown	unknown	gnl\|CDD\|181025
NZ_CP030771.1\|WP_138962980.1\|7975797_7976328_-\|DUF309-domain-containing-protein	unknown	unknown	gnl\|CDD\|377120
NZ_CP030771.1\|WP_138967338.1\|7986419_7987697_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138962985.1\|7978037_7979390_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP030771.1\|WP_138963000.1\|7989814_7990132_+\|AzlD-domain-containing-protein	unknown	unknown	gnl\|CDD\|377512
NZ_CP030771.1\|WP_138962978.1\|7975008_7975785_-\|precorrin-6A-synthase-(deacetylating)	unknown	unknown	gnl\|CDD\|236218
NZ_CP030771.1\|WP_171075913.1\|7990167_7993455_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276938
NZ_CP030771.1\|WP_138962998.1\|7989089_7989818_+\|AzlC-family-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|377070
NZ_CP030771.1\|WP_138962987.1\|7979464_7980445_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224096
NZ_CP030771.1\|WP_171075914.1\|7993959_7994385_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|226158
NZ_CP030771.1\|WP_138967336.1\|7985868_7986402_+\|bacilysin-biosynthesis-protein-BacA	unknown	unknown	gnl\|CDD\|270350
NZ_CP030771.1\|WP_138962976.1\|7972492_7972690_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_138962989.1\|7980441_7981320_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223472
NZ_CP030771.1\|WP_138962994.1\|7987732_7988167_+\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915
NZ_CP030771.1\|WP_138967334.1\|7981343_7982324_+\|hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240644
NZ_CP030771.1\|WP_138963009.1\|7994818_7995358_+\|FABP-family-protein	unknown	unknown	gnl\|CDD\|378046
NZ_CP030771.1\|WP_138963004.1\|7993550_7993889_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	unknown
NZ_CP030771.1\|WP_171075912.1\|7972882_7974931_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP030771.1\|WP_138962974.1\|7971283_7972471_+\|acetyl-CoA-C-acyltransferase	unknown	unknown	gnl\|CDD\|238383
NZ_CP030771.1\|WP_138962983.1\|7976683_7977778_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|380483

Protein	Function_ID	Function_description	E-value
NZ_CP030771.1\|WP_138962980.1\|7975797_7976328_-\|DUF309-domain-containing-protein	gnl\|CDD\|377120	pfam03745, DUF309, Domain of unknown function (DUF309). This domain is found in eubacterial and archaebacterial proteins of unknown function. The proteins contain a motif HXXXEXX(W/Y) where X can be any amino acid. This motif is likely to be functionally important and may be involved in metal binding.	1.15241e-22
NZ_CP030771.1\|WP_138962994.1\|7987732_7988167_+\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	1.05822e-07
NZ_CP030771.1\|WP_138962985.1\|7978037_7979390_+\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.61104e-51
NZ_CP030771.1\|WP_138963000.1\|7989814_7990132_+\|AzlD-domain-containing-protein	gnl\|CDD\|377512	pfam05437, AzlD, Branched-chain amino acid transport protein (AzlD). This family consists of a number of bacterial and archaeal branched-chain amino acid transport proteins. AzlD is known to be involved in conferring resistance to 4-azaleucine although its exact role is uncertain.	2.4329e-05
NZ_CP030771.1\|WP_138962978.1\|7975008_7975785_-\|precorrin-6A-synthase-(deacetylating)	gnl\|CDD\|236218	PRK08284, PRK08284, precorrin 6A synthase; Provisional.	5.31466e-138
NZ_CP030771.1\|WP_171075913.1\|7990167_7993455_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	1.01105e-39
NZ_CP030771.1\|WP_138962998.1\|7989089_7989818_+\|AzlC-family-ABC-transporter-permease	gnl\|CDD\|377070	pfam03591, AzlC, AzlC protein.	1.0023e-28
NZ_CP030771.1\|WP_138962987.1\|7979464_7980445_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.24074e-57
NZ_CP030771.1\|WP_171075914.1\|7993959_7994385_-\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|226158	COG3631, COG3631, Ketosteroid isomerase-related protein [General function prediction only].	5.76767e-16
NZ_CP030771.1\|WP_138967336.1\|7985868_7986402_+\|bacilysin-biosynthesis-protein-BacA	gnl\|CDD\|270350	cd13632, PBP2_Aa-PDT_like, Catalytic domain of prephenate dehydratase from Arthrobacter aurescens and similar proteins, subgroup 3; the type 2 periplasmic binding protein fold. Prephenate dehydratase (PDT, EC:4.2.1.51) converts prephenate to phenylpyruvate through dehydration and decarboxylation reactions. PDT plays a key role in the biosynthesis of L-Phe in organisms that utilize the shikimate pathway. PDT is allosterically regulated by L-Phe and other amino acids. The catalytic PDT domain consists of two similar subdomains with a cleft in between, which hosts the highly conserved active site. In gram-postive bacteria and archaea, PDT is a monofunctional enzyme, consisting of a catalytic domain (PDT domain) and a regulatory domain (ACT) (aspartokinase, chorismate mustase domain). In gram-negative bacteria, PDT exists as fusion protein with chorismate mutase (CM), forming a bifunctional enzyme, P-protein (PheA). The CM in the P-protein catalyzes the pericycle isomerization of chorismate to prephenate that serves as a substrate for PDT. The CM and PDT are essentail enzymes for the biosynthesis of aromatic amino acids in microorganisms but are not found in humans. Thus, both CM and PDT can potentially serve as drug targets against microbial pathogens. The PDT domain has the same structural fold as the type 2 periplasmic binding proteins (PBP2), many of which are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.18284e-05
NZ_CP030771.1\|WP_138962996.1\|7988163_7989093_+\|branched-chain-amino-acid-transaminase	gnl\|CDD\|181025	PRK07544, PRK07544, branched-chain amino acid aminotransferase; Validated.	4.47965e-143
NZ_CP030771.1\|WP_138962989.1\|7980441_7981320_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.07001e-65
NZ_CP030771.1\|WP_138967334.1\|7981343_7982324_+\|hydroxyacid-dehydrogenase	gnl\|CDD\|240644	cd12167, 2-Hacid_dh_8, 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.	4.27295e-127
NZ_CP030771.1\|WP_138963009.1\|7994818_7995358_+\|FABP-family-protein	gnl\|CDD\|378046	pfam08768, DUF1794, Domain of unknown function (DUF1794). This domain forms a beta barrel structure but the function is unknown. The GO annotation for this protein indicates that the protein has a function in nematode larval development and has a positive regulation on growth rate.	4.48751e-57
NZ_CP030771.1\|WP_171075912.1\|7972882_7974931_-\|MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	7.14351e-76
NZ_CP030771.1\|WP_138962974.1\|7971283_7972471_+\|acetyl-CoA-C-acyltransferase	gnl\|CDD\|238383	cd00751, thiolase, Thiolase are ubiquitous enzymes that catalyze the reversible thiolytic cleavage of 3-ketoacyl-CoA into acyl-CoA and acetyl-CoA, a 2-step reaction involving a covalent intermediate formed with a catalytic cysteine. They are found in prokaryotes and eukaryotes (cytosol, microbodies and mitochondria). There are 2 functional different classes: thiolase-I (3-ketoacyl-CoA thiolase) and thiolase-II (acetoacetyl-CoA thiolase). Thiolase-I can cleave longer fatty acid molecules and plays an important role in the beta-oxidative degradation of fatty acids. Thiolase-II has a high substrate specificity. Although it can cleave acetoacyl-CoA, its main function is the synthesis of acetoacyl-CoA from two molecules of acetyl-CoA, which gives it importance in several biosynthetic pathways.	0
NZ_CP030771.1\|WP_138962983.1\|7976683_7977778_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|380483	cd01541, PBP1_AraR, ligand-binding domain of DNA transcription repressor specific for arabinose (AraR) which is a member of the LacI-GalR family of bacterial transcription regulators. Ligand-binding domain of DNA transcription repressor specific for arabinose (AraR) which is a member of the LacI-GalR family of bacterial transcription regulators. The ligand-binding domain of AraR is structurally homologous to the periplasmic sugar-binding domain of ABC-type transporters and both domains contain the type 1 periplasmic binding protein-like fold. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the type 1 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	1.16652e-55

>NZ_CP030771.1|WP_138967334.1|7981343_7982324_+|hydroxyacid-dehydrogenase
MSSRAAAAVFAPRALAALAEVCDLAPPPALDDLTSARARSVLADVEVLVTGWGCPPLDAGVLAAAPRLKAVVHAAGSVRGHVTDACWERGLAVSSAAAANALPVAEYTLAMILLHGKHVLEQARDYRRARERGDWLRTPHHVGNYRRTVGILSASLIGRRVIELLRPFDFEVLLHDPYVTAAQAAELGAERVTLPALFARGDLVSVHTPLLPATRGLVDRELLVSMRPGATLINTSRGAVVDQDALTDVVRAGRIRAVLDVTDPEVLPAAHPLWDCPNALLTPHLAGSQGSEWQRLADTAVGEVARWAAGEGLAHPVRRERLAYLA
>NZ_CP030771.1|WP_138962989.1|7980441_7981320_+|ABC-transporter-permease-subunit
MSASHSASSHSASSRPCLLGRATVNAVVGLFVLYTLLPVLWLVLAATKTRDALFSSSLLSFGDFSLTRNVKDVFAMDGGLYGRWYGNSLLYAVLGAALGSLISVACGYAFDKYRFRHKEKLFGLVLAAVMVPQTVLALPLYLLASEAGLVNTFWAVFIPVLFNPFGVYLGRIFSQGYVPDEVLEAARVDGAGELTTYVRVSLRMLGPGLVTVFLFQLTAIWNNFFLPMVMLSDQDLYPVSLGLYQWNSQATVSPEYYPVVITGSLLAVVPLLLAFALLQRFWRSGLTAGAVK
>NZ_CP030771.1|WP_138962987.1|7979464_7980445_+|ABC-transporter-permease-subunit
MTATAHVPAAAAPQRAAERRGQKAKRMAARRRRTAAGVLMAPFLLLLAVVFLVPVGTAVWLSFFSDDQPGLGFGPERTVFVGARSYAAVLGDPTFLSGLGTVALYCLLYIPLMVLGSLALALLLDSGVVRLRAWAQLGLFLPHAVPGIIAALIWLYLYTPGISPVIDVLNKADITVDFLGLHTTLPSIVNIALWSNLGYNMVVFYAALQAVPREVVEASVVDGAGPVRTALQVKTPLVRSSIVVVAMFTLIWALQLFTEPMLLSQSSQMINSRFSPSMYIYDAAFTRNNYSLAAAASVILLALTVAVSYGVTRWTSRSDRTEGAAR
>NZ_CP030771.1|WP_138962985.1|7978037_7979390_+|extracellular-solute-binding-protein
MPGRHSRPSRRGVLAAATALPLTGALGACGGGGAAPRAKGAKGAKGVTTLTFWSALRGSQEVVDAFNRTHDHIRVDFEQVPSGNHGGYAKLSNAARAGNAPDVATIEYPQVPGFAIDGVARDITPLLGAGLRARLLPQALGLTTFERRTYSVPLDVEPMVLHYRQDLFDKYGFDVPATWEEFAELARKVPGRGEGRRAAVFATDGAMHFAAWAWQAGAQWFDTSKGAWNVSLADAPTRRVAAYWQRLIDEDLVHVNAVESRLFDAQVAGGQVLTRFSGAWEAGAQMNARPAQKGLWRIAPLPQWDPDRPAIGTHGGSTFAVTKDARHPEAAMEFIEWQVSHPDALKARLSSGASSQYPAATDLVAVGRAAFDRGYYGGQDVYALFDEEARKIRDGWVWGPRMTATSKVMQDAFARAGGGSGTVLSSVRAAQDGTMPDLKALGLATTQHST
>NZ_CP030771.1|WP_138962983.1|7976683_7977778_+|substrate-binding-domain-containing-protein
MREPVDLRRQRILAAVRSRGATRVSDLAAELAVSVVTLRRDVEELAREGKLRRGHGVARPVTDEAERPAPPAPAGDGGPVAVVVPERHSYLYETLHGARAAFEEAGVRIALHIAPAAPGAEQPLVERALADGARGLLIAPRWRDRATEEADCAWLARVPVPLVVMERRPRRGSALHAVDAVCTDHWYGVHLAVEHLTGLGHRRIVLAARDDSPTARALRAAFTEIAADHPDVHEWALALSSPGAVPDPAAPTAEQPVDLPGLLGATGATAAVLHGDVDALMLVQALRDSGVRVPEDCSVIAYDDVVAALGSTPLTAVSPPKADIGRAAAELLLRRLARGAEPVRRLELLPELKVRGSTRPLRGA
>NZ_CP030771.1|WP_138962980.1|7975797_7976328_-|DUF309-domain-containing-protein
MTSALGPGGRDRDTEGRARSARPRDGLGRPLPYGAEGVERQPEGVTRTPARTLAEAQALLDAGRPFHAHEVFEDAWKSGPERERGLWQGLAQLAVGLTHAARGNATGGARLLRRGAGAVAEWSAAGPGRERPYGIGVAELVEWARGLAARVERGEVPLDAAAAAPTLAPGTTRGDG
>NZ_CP030771.1|WP_138962978.1|7975008_7975785_-|precorrin-6A-synthase-(deacetylating)
MRRIHVIGIGAGDPDQLTLQAVKAMKDTEVFFVLDKGEDKEDLVALRRGMLDAHRPDGAYRVVEARDPRRAQEADRVAYAGAVDDWRGRRADIYERLIAEELGAEGTGAFLVWGDPALYDSTIAILEDVIGRGAVAFSYAVVPGVSSVSALAARHRVGLNRVGRPFQVTTGRRLSDEGFPEGVDDVVVMLDARQAFLRYADRDDLDIYWGAYLGTPDEILVSGALPEAAGRIARLRAEARARKGWIMDTYLLRRRPRD
>NZ_CP030771.1|WP_171075912.1|7972882_7974931_-|MFS-transporter
MTVTEHAEAARAPEQGPPVLDRRRRNVVFVTIMLGVLLAALDQTIVGTALPTIVSDLGGAAHMSWVVTSYLLAETVATVLVGKFGDLFGRKVVFQVSAVVFITGSFLCGLATNMSLLIAWRAMQGIGAGGLMVTSMALIADVIPLRERGKYQGAIGAVFGVSTVIGPLLGGLFTDHLSWRWAFYVNVPIAVLVVVAAARTIPSVKSAARPVIDYLGIALVAIGSSALILATSWGGNEYAWGSGVIIGLFAGGLAALAGFCWAETRAAEPMLPMRLFANPVFTVCSVLSFIVGFAMLGAMTFLPTYLQYVDGDSATISGVRTLPMVVGLLIASIFSGNVVSRTGTYRIFPIVGALVMALGLFLMSLMGSATSAWLESLYMFVLGVGIGLCMQVLTIAVQNTVAYADLGTATSGVTFFRTLGSSFGTAVFGTIYANTLAPNLRDGVAEAARTGAAPQEAIAKASQSPEGLHELPGAAAAPLVEAYADTLQTVFLWTVPVAAVGFVVALFLKQVELRDSARMSSNDMGEGFASPSSAGDSARLLELAVGNILRHKGAGTARTVVSRSDTRLDPAGAWAVMQVALFTRLVGHANLNLIAARRRLPPEVLVPVFDRMVEEGYLSRSGTLFQHTPAGEREAGVIGKEWARWLAEELEKDGRGSEDDAALTTAVDTIAKRLLAEDLNTP
>NZ_CP030771.1|WP_138962976.1|7972492_7972690_-|hypothetical-protein
MGMETDGAIHQVHARLVGAYWLDSPYLRHPRCCCCAPARPARPWGVTAVGLACLALALTVAVTLM
>NZ_CP030771.1|WP_138962974.1|7971283_7972471_+|acetyl-CoA-C-acyltransferase
MRTVHFAAARRTPIGRLRGALSSVRPDDLAATVVRGLLDGVPDLDPARVDDVYWGAANQAGEDNRNVARMAALLAGLPESVPGATVNRLCASGLEAVTTAARAIAAGEADIVVAGGSESMSRAPFVLPRPDEALPHRMETVDTRLGWRLVNPRMRELHGLLSMGETAEEVAERHGVSRERQDAFALRSHQRAAAARKDGRFDAELLPVTTPDGTLVDTDEGIREDTSYEKLSKLRPVFRDGGSVTAGNASPMNDGAAGLLLVSEEALRDLGLTSLGRYAAGASAGVHPDVMGIGPVPATRKALARLGWSVADVQEAEVNEAFAAQAIASVDTLGIDPDLVNPDGGAIALGHPLGCSGARILTTLLHRMGRTGATRGLATMCVGVGQGSAVLVERD
>NZ_CP030771.1|WP_138967336.1|7985868_7986402_+|bacilysin-biosynthesis-protein-BacA
MGDIRYLHTLGPTGTNLESAAHLWFQRHGLEDEGQVVLHPSLEDAMASVPRTGAHALVACAVYPELHTLVFGNLHTCRMVDCFLWPTYEMVLAAAPGTHGEPRTVATHPAPAGLVAPVSARQLVTSNAQAAIDCADGKAEGCVTTVVAARAHGLRIVRSFGEVPMVYTVHQVREAAR
>NZ_CP030771.1|WP_138967338.1|7986419_7987697_+|hypothetical-protein
MLGPASGTHHLHDDLLGEAARLGSGLLPRVNAFRRRQRDDGTVPAPDAADRRALLAVTDEATRFFAGHGRAAQADALAADVEGWLAAGLDTPPHFARSRDALTAPADGDWAAFLAPVQTTNSAPPVGKRLEFFLVRRKEPDALPGLAEHYPHPKNNCQATVLVAGSEGVADGNCIVFFPENVAAHDKVVEQAYAIFFFSKFRRIHETYAVPSARAVLTPRSVPRASTGMDPEACYQARAVWGYLHDYFHHQGRWPLDQHIKLKMNWFVGLLEELKVDARTALACHADPAVPYADEQIAMILLERMFRYPLDAHAVRNFDAGTGVFLYSWLRERRALATGRAGLLHLDHDRVIEGLRELVDAIEGMEAAVSTPAEYRAAAKALVRTRLREGAEGDRYAFTDDQRALLRERERLAALPPLRFAPAAL
>NZ_CP030771.1|WP_138962994.1|7987732_7988167_+|nuclear-transport-factor-2-family-protein
MGKLDRAAMEAAVRQYFEACNKVDRDLFAACLSEDVVHYLAHGMSGPVHGIDPIVERWGADVRANDSHWAVDAVYADEHTRTAVCEWTAFKPRLGKVLRGAEVYRFDDTGLIDEVRIYYASARDDTRAANELEGFPYADRGFAT
>NZ_CP030771.1|WP_138962996.1|7988163_7989093_+|branched-chain-amino-acid-transaminase
MTGAAPPLDDRDGVLWVDGALVPWRAARLHVLSHGLHYGGSVFEGERVYDGRVFALHDHSARLVASARHLGYELPWTADELDAVTREVVAAAGLTDGYVRPVAWRGADTLRLVAPDNRVHLAVAAWPWPRIFTDGPRGIRLGTSRWRRPAPDTAPIRAKAAALYAVGALAGQEAEAAGFDDALLLDHRGRLAEATGANLFLVRDGELHTPPPECVLDGITRRTVIGLARDLGLPVVERHLDPAELDRADEVFLTGTAYEVQPVTGIDDRTFPLGEVGGALTEAYARAVRAGDGDRAAPPAPAAASSDTG
>NZ_CP030771.1|WP_138962998.1|7989089_7989818_+|AzlC-family-ABC-transporter-permease
MTGSGSTGSPRSSRGPGTDGGRRAAWAEGARAAVPFTVAIFAFGVSFGVLAKGAGFSALAATSMSGLVFVGSSQFAAVSVIVNGGGWAAAAVAGTLLNLRYLVMGFAILPALRGGRARRAVESQLVIEESWAIASDADGRFDRVRLLSSGVVLWLGWVLGTLAGAIGPFRAVDVLNYGLDAVSPVLFFLLLAPHLGTARKRSAAATAAVAAAVLTAVAVPDSAIAVACLVAVGWTWRAGRKP
>NZ_CP030771.1|WP_138963000.1|7989814_7990132_+|AzlD-domain-containing-protein
MSNDPWIVVGALVVTTFLIKGAGSLVLGDRELPAWFPRFVEYLTPALLAVLVVTQLVGSAGAHGMTFDARVAGFAGALVAWRLKAPVPLVVLVAAAVTAGVRALG
>NZ_CP030771.1|WP_171075913.1|7990167_7993455_-|tetratricopeptide-repeat-protein
MSRISEPQEAQAPKESVRIRLLGPVSVEVQGRHVGLGPQQRALLAALALARGPVSTSRLAELLWEGEIPDGAVSSLRTHVLHLRRILEPGRRATSGFEVLVSAGARSNTSYTLQVADGQVDALRFVHLTDRARKAAADGDAPAVVTLLDEALALWTGPALEGVSDRSFALAETDRLEELRLVAREDRVDALIELGRYEASLAELTTLVRAFPLRERLRRQLMLALYRSGRQADALAAYRDFYQLLDDEVGIEPGRQLKELHQRVLVGDPALAPERSPAPAAPPAARPVPRQLPPDVASFTGRADQLRELDTLLSRYDTGPGQTLVISSVSGMAGVGKTALAVHWMHRVADRFPDGQLYANLRGHAAEPPTTADEALGQLLRALGVGTGHLPESTDEKAALYRSLLAGKRVLILLDDAAGLEQVRPLLPGSPTCFVVVTSRNDLRGLTAFHDAHRVSLAVFAEDEALALLGRVIGADRVRGEPEAAAEAVRLCGLLPLAVRIVAAHLIGDRHLPIARIVGQLRADRLGELALDQERHTGVRSVLALSYRSLPAPEREALRLLALAPGPEVSVPAAAALTGAAVPATTRLLDQLAARSLLETHRPGRFHLHALVRLFAGERAAAEDAPAVRDDAVGRLLTWYLGTAEQAACRLYGTFYSWYAARPPEPDGSPTAPLAFRSDAAARAWLDDERPALLACAQHAVRHGPRPFAWKSALAVHGHLMEHGRRTDWLRAAHAGLKAAEAEHDDHARAVMHWSLCYVLWELARHEEALEHSAAADELFARAGQPVERAGAVLGLAASHRERGALDQAVRDAERALALYREGAQPAGEAWALFLLGRARLDQGRLDAARGHFAAAGACAEASADQHTVMLSLWGRASVQHALGALEEAQRLLTRALAVDGRLLATYAAEGALNALAVVCRDLGDPRLALKYAVDALGVTHRTRRRLVEPDALNTIGTVLLRLDDVPGALDHHRRALDAARAACCRRAEAEACLGLAAVHRQLGESREALACTRRALSTARQAGLGLAEGAALTELARVHLALGQHAKAARAAERSARLHRATGHRPGLDEALEVAAAVERAGAAAAGPPEAGAG
>NZ_CP030771.1|WP_138963004.1|7993550_7993889_-|nuclear-transport-factor-2-family-protein
MTSSSGRPSHPAVRAFVDAVNAQDQQALWTVLAEDATVIDVGTERDLHAWVERELFSSHARMEVVRESPDGLSVSARFHNDIWNDIDTAWEFTVSDGVIRRFVTGPDESGSG
>NZ_CP030771.1|WP_171075914.1|7993959_7994385_-|nuclear-transport-factor-2-family-protein
MSTHSPEASARATREVIDAYLARLADRDLDGAVRLFAESAEFLAPGSPAVPWSGHHTGHKGVAHFFATLHEYLQPEEFTVTHIVVDGEHGVIIGHLRDTVKATGKPLTTPFAAHLTVVDGRVARYHLFEDTHALHRAVTDG
>NZ_CP030771.1|WP_138963009.1|7994818_7995358_+|FABP-family-protein
MQPVPDLPFPDAHRPDDAPAPHPLLAPVTELLGTWHGLGDGGYPTLDGDFAYAQEVTFRHDGRPFLRYEARAWILDADGAPLRPAARESGWWRLQADGHVEAVISQPTGIVEVATGVAADRTVDVSTHQVALTPTAKRVDATRRRYALADDGTLTFTHDLAAVGQPLQHHLSATLRRAR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP030771_1	1.1\|255975\|38\|NZ_CP030771\|CRISPRCasFinder	255975-256012	38	NZ_CP030771.1	256011-256048	0	1.0
NZ_CP030771_3	3.1\|1206644\|19\|NZ_CP030771\|CRISPRCasFinder	1206644-1206662	19	NZ_CP030771.1	3562558-3562576	1	0.947

1. spacer 1.1|255975|38|NZ_CP030771|CRISPRCasFinder matches to position: 256011-256048, mismatch: 0, identity: 1.0

aaggtggtactgcgatcgaaggcggtgcgacgactgaa	CRISPR spacer
aaggtggtactgcgatcgaaggcggtgcgacgactgaa	Protospacer
**************************************

2. spacer 3.1|1206644|19|NZ_CP030771|CRISPRCasFinder matches to position: 3562558-3562576, mismatch: 1, identity: 0.947

tggctgacgcgggcggcgc	CRISPR spacer
tggctgacgtgggcggcgc	Protospacer
*********.*********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	MN842294	Leclercia adecarboxylata strain G426 plasmid pG426-FII, complete sequence	58218-58245	4	0.857
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_MH909329	Leclercia adecarboxylata strain 150707804 plasmid p707804-3FII, complete sequence	91965-91992	4	0.857
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP015007	Aminobacter aminovorans strain KCTC 2477 plasmid pAA02, complete sequence	80735-80762	5	0.821
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_LR134465	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence	308097-308129	6	0.818
NZ_CP030771_16	16.2\|7641829\|28\|NZ_CP030771\|CRISPRCasFinder	7641829-7641856	28	NZ_CP019037	Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence	55954-55981	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NC_017966	Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence	263523-263550	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022775	Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence	1598272-1598299	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	11021-11048	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	1516491-1516518	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP015420	Rhodovulum sulfidophilum DSM 1374 plasmid unnamed2, complete sequence	95754-95781	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP023017	Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence	1588398-1588425	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	1515513-1515540	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	1516483-1516510	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	1515841-1515868	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	1516473-1516500	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022764	Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence	1598440-1598467	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022797	Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence	1598423-1598450	6	0.786
NZ_CP030771_16	16.3\|7641883\|28\|NZ_CP030771\|CRISPRCasFinder	7641883-7641910	28	NZ_CP022758	Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence	1598402-1598429	6	0.786
NZ_CP030771_4	4.1\|2554425\|31\|NZ_CP030771\|CRISPRCasFinder	2554425-2554455	31	MN379638	Chicken microvirus mg7_7, complete genome	3660-3690	8	0.742
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_CP024425	Paracoccus yeei strain TT13 plasmid pTT13-3, complete sequence	67011-67043	8	0.758
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_CP031081	Paracoccus yeei strain CCUG 32053 plasmid pYEE3, complete sequence	109283-109315	8	0.758
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	353989-354021	8	0.758
NZ_CP030771_15	15.4\|6205788\|36\|NZ_CP030771\|CRT	6205788-6205823	36	NZ_CP034352	Streptomyces sp. W1SF4 plasmid p2, complete sequence	155674-155709	8	0.778
NZ_CP030771_15	15.4\|6205788\|36\|NZ_CP030771\|CRT	6205788-6205823	36	NC_030917	Gordonia phage OneUp, complete genome	16491-16526	8	0.778
NZ_CP030771_15	15.6\|6205908\|39\|NZ_CP030771\|CRT	6205908-6205946	39	NZ_CP013855	Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence	189258-189296	8	0.795
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	402885-402917	9	0.727
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_CP049358	Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence	75057-75089	9	0.727
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NZ_CP031159	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence	61214-61246	9	0.727
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NC_010627	Paraburkholderia phymatum STM815 plasmid pBPHY02, complete sequence	412139-412171	9	0.727
NZ_CP030771_15	15.3\|6205731\|33\|NZ_CP030771\|CRT	6205731-6205763	33	NC_006569	Ruegeria pomeroyi DSS-3 megaplasmid, complete sequence	468257-468289	9	0.727
NZ_CP030771_15	15.6\|6205908\|39\|NZ_CP030771\|CRT	6205908-6205946	39	NZ_CP016082	Streptomyces sp. SAT1 plasmid unnamed2, complete sequence	180042-180080	13	0.667

1. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to MN842294 (Leclercia adecarboxylata strain G426 plasmid pG426-FII, complete sequence) position: , mismatch: 4, identity: 0.857

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
agcctgccgacgccacgggggcgactga	Protospacer
**.******* **************.*.

2. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_MH909329 (Leclercia adecarboxylata strain 150707804 plasmid p707804-3FII, complete sequence) position: , mismatch: 4, identity: 0.857

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
agcctgccgacgccacgggggcgactga	Protospacer
**.******* **************.*.

3. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP015007 (Aminobacter aminovorans strain KCTC 2477 plasmid pAA02, complete sequence) position: , mismatch: 5, identity: 0.821

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
actctgccaaggccacgggggcgacgtc	Protospacer
* ******.****************

4. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_LR134465 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence) position: , mismatch: 6, identity: 0.818

gaccgacggccgccccggcctgtccg-acgccgc	CRISPR spacer
cgccgacggccgccccgggctggccgcacgcgg-	Protospacer
 .**************** *** *** **** *

5. spacer 16.2|7641829|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP019037 (Massilia putida strain 6NM-7 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.786

gggtggccgggtccaccgggtcactcga	CRISPR spacer
gcgtggccgggtccatcgggtcaccgac	Protospacer
* *************.********. .

6. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NC_017966 (Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
gctctgccgtggccacgggggcgatctt	Protospacer
. ******* **************.*

7. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022775 (Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

8. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
cgctggccgaggacgcgggggcgaccgg	Protospacer
 *.. ******* *.*************

9. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

10. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP015420 (Rhodovulum sulfidophilum DSM 1374 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tgagtgccgagggcaagggggcgaccga	Protospacer
 *  ******** ** ***********.

11. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP023017 (Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

12. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

13. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

14. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

15. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

16. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022764 (Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

17. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022797 (Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

18. spacer 16.3|7641883|28|NZ_CP030771|CRISPRCasFinder matches to NZ_CP022758 (Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.786

agtctgccgaggccacgggggcgaccgg	CRISPR spacer
tacccgccgatgccacgcgggcgaccgg	Protospacer
 ..*.***** ****** **********

19. spacer 4.1|2554425|31|NZ_CP030771|CRISPRCasFinder matches to MN379638 (Chicken microvirus mg7_7, complete genome) position: , mismatch: 8, identity: 0.742

cgggcgggaaagaaacgccgcggagcggcgc	CRISPR spacer
attgcctgaaagaatcgccgcgaagcggcga	Protospacer
   **  ******* *******.*******

20. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_CP024425 (Paracoccus yeei strain TT13 plasmid pTT13-3, complete sequence) position: , mismatch: 8, identity: 0.758

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
cgccggcggccgcccctgcctgtccgatccgga	Protospacer
 .***.********** **********. * *

21. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_CP031081 (Paracoccus yeei strain CCUG 32053 plasmid pYEE3, complete sequence) position: , mismatch: 8, identity: 0.758

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
cgccggcggccgcccctgcctgtccgatccgga	Protospacer
 .***.********** **********. * *

22. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.758

gaccgac---ggccgccccggcctgtccgacgccgc	CRISPR spacer
---ctacctgggccgccccggcctgaccgccgcccg	Protospacer
   * **   *************** *** ****

23. spacer 15.4|6205788|36|NZ_CP030771|CRT matches to NZ_CP034352 (Streptomyces sp. W1SF4 plasmid p2, complete sequence) position: , mismatch: 8, identity: 0.778

cagctaccccggcgcggccgcccccgcgcccgcagc	CRISPR spacer
caccacccccgccccggccgcccccgcgcccgcgca	Protospacer
** *  ***** * *******************.

24. spacer 15.4|6205788|36|NZ_CP030771|CRT matches to NC_030917 (Gordonia phage OneUp, complete genome) position: , mismatch: 8, identity: 0.778

-cagctaccccggcgcggccgcccccgcgcccgcagc	CRISPR spacer
gcaggcg-acgggcgggtccgcccccgcgcccgcagc	Protospacer
 *** ..  * **** * *******************

25. spacer 15.6|6205908|39|NZ_CP030771|CRT matches to NZ_CP013855 (Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence) position: , mismatch: 8, identity: 0.795

cgccccggcggccccggcggccccggtggccccggtggc	CRISPR spacer
ccgcgccacggccccgtcggccccggtgcccccggtgcc	Protospacer
*  * * .******** *********** ******** *

26. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 9, identity: 0.727

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
agccgccggccgccccggcctgcccgaccgaaa	Protospacer
..*** ****************.*****   .

27. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_CP049358 (Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
cgaggacgaccgccccggcctgcccgacgaggt	Protospacer
 .  ****.*************.******  *.

28. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NZ_CP031159 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence) position: , mismatch: 9, identity: 0.727

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
cgaggacgaccgccccggcctgcccgacgaggt	Protospacer
 .  ****.*************.******  *.

29. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NC_010627 (Paraburkholderia phymatum STM815 plasmid pBPHY02, complete sequence) position: , mismatch: 9, identity: 0.727

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
aagtcacggccgcctctgcctgtccgacgacat	Protospacer
.* . *********.* ************ *..

30. spacer 15.3|6205731|33|NZ_CP030771|CRT matches to NC_006569 (Ruegeria pomeroyi DSS-3 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.727

gaccgacggccgccccggcctgtccgacgccgc	CRISPR spacer
ccctgacggccaccccggcctgaccgaccttgg	Protospacer
  *.*******.********** ***** ..*

31. spacer 15.6|6205908|39|NZ_CP030771|CRT matches to NZ_CP016082 (Streptomyces sp. SAT1 plasmid unnamed2, complete sequence) position: , mismatch: 13, identity: 0.667

cgccccggcggccccggcggccccggtggccccggtggc---------	CRISPR spacer
---------ggccccggcggtcccggcggtcccggtggggcgtaccgg	Protospacer
         ***********.*****.**.********

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

482333 : 530673

Bacillus_phage(33.33%)

tRNA,plate,tail,holin

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_138957603.1\|482333_483137_-\|tRNA	tRNA-dependent cyclodipeptide synthase	NA	NA	NA	NA
WP_138957604.1\|483560_484220_+	DUF4360 domain-containing protein	NA	NA	NA	NA
WP_138957605.1\|484343_485003_-	DUF1707 domain-containing protein	NA	NA	NA	NA
WP_138957606.1\|485290_487699_+	hypothetical protein	NA	NA	NA	NA
WP_138957607.1\|488012_488786_+	hypothetical protein	NA	NA	NA	NA
WP_138965912.1\|489006_490110_+	serine hydrolase	A5YJY7	Mycobacterium_phage	6.3e-22	28.1
WP_138957608.1\|490154_490643_-	hypothetical protein	NA	NA	NA	NA
WP_138957609.1\|490769_491804_-	sulfotransferase	NA	NA	NA	NA
WP_138957610.1\|491947_493426_-	MFS transporter	NA	NA	NA	NA
WP_138957611.1\|493658_494663_+	YdcF family protein	NA	NA	NA	NA
WP_138957612.1\|494711_495635_-	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_138965914.1\|495771_496185_+	MerR family transcriptional regulator	NA	NA	NA	NA
WP_138957613.1\|496516_497263_+	VCBS repeat-containing protein	NA	NA	NA	NA
WP_171076043.1\|497421_498021_+	response regulator transcription factor	NA	NA	NA	NA
WP_138957615.1\|498181_498859_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_138957616.1\|498855_500883_+	AAA family ATPase	A0A0R6PCP6	Moraxella_phage	1.5e-21	33.9
WP_138957617.1\|500933_502337_-	hydrolase	NA	NA	NA	NA
WP_138957618.1\|502593_504189_+\|tail	phage tail sheath subtilisin-like domain-containing protein	J9PVC2	Bacillus_phage	3.3e-64	32.8
WP_138957619.1\|504261_504705_+\|tail	phage tail protein	NA	NA	NA	NA
WP_138957620.1\|504704_505211_+	hypothetical protein	NA	NA	NA	NA
WP_171075611.1\|505207_505366_+	hypothetical protein	NA	NA	NA	NA
WP_138957621.1\|505449_506352_-	hypothetical protein	NA	NA	NA	NA
WP_138957622.1\|508027_508534_+	extensin	NA	NA	NA	NA
WP_138965916.1\|508586_509009_+\|tail	phage tail protein	NA	NA	NA	NA
WP_138957623.1\|509051_509771_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_138957624.1\|509770_511654_+	VgrG-related protein	NA	NA	NA	NA
WP_138957625.1\|511686_512136_+	GPW/gp25 family protein	A0A1D7SP91	Cyanophage	3.9e-10	30.5
WP_138957626.1\|512135_514094_+\|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_138957627.1\|514122_514680_+\|tail	phage tail protein	NA	NA	NA	NA
WP_138957628.1\|514676_516005_+	discoidin domain-containing protein	NA	NA	NA	NA
WP_138957629.1\|516183_518199_+	FAD/NAD(P)-binding protein	NA	NA	NA	NA
WP_138957630.1\|518217_518994_+	L-iditol 2-dehydrogenase	NA	NA	NA	NA
WP_138957631.1\|519028_520399_+	glycosyltransferase family 4 protein	NA	NA	NA	NA
WP_138957632.1\|520410_521595_+	MFS transporter	NA	NA	NA	NA
WP_138957633.1\|521591_522404_+	acetoacetate decarboxylase family protein	NA	NA	NA	NA
WP_138957634.1\|522400_522940_+	5'(3')-deoxyribonucleotidase	NA	NA	NA	NA
WP_138957635.1\|523017_523431_-	ANTAR domain-containing protein	NA	NA	NA	NA
WP_171075612.1\|523534_523924_-	response regulator	W8CYM9	Bacillus_phage	1.8e-08	33.3
WP_138957637.1\|524311_524539_-	DUF5133 domain-containing protein	NA	NA	NA	NA
WP_138957638.1\|524657_524903_-	CsbD family protein	NA	NA	NA	NA
WP_138957639.1\|524872_526165_-	carboxylesterase family protein	A0A0M4JT58	Mollivirus	9.7e-30	36.3
WP_138957640.1\|526186_526996_-	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_138957641.1\|529912_530113_+	hypothetical protein	NA	NA	NA	NA
WP_138965918.1\|530301_530673_+\|holin	phage holin family protein	NA	NA	NA	NA

DBSCAN-SWA_2

2473291 : 2481302

Mycobacterium_phage(50.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138966304.1\|2473291_2475136_-	DNA polymerase	A0A2P1CHS7	Mycobacterium_phage	2.7e-134	45.6
WP_138958951.1\|2475200_2475749_-	hypothetical protein	NA	NA	NA	NA
WP_138958952.1\|2475761_2476307_-	hypothetical protein	NA	NA	NA	NA
WP_171075687.1\|2476303_2477119_-	metallophosphoesterase	G8I7S5	Mycobacterium_virus	1.3e-72	55.0
WP_138958954.1\|2477115_2477484_-	hypothetical protein	NA	NA	NA	NA
WP_138958955.1\|2477480_2478149_-	topoisomerase	A0A249XU42	Mycobacterium_phage	5.5e-45	46.4
WP_138958957.1\|2478528_2478807_-	hypothetical protein	NA	NA	NA	NA
WP_138958958.1\|2478799_2479234_-	hypothetical protein	A0A159B6U4	Tsukamurella_phage	2.7e-16	43.6
WP_138958959.1\|2479233_2479572_-	hypothetical protein	NA	NA	NA	NA
WP_138958960.1\|2479595_2480429_-	AAA family ATPase	Q5J5G2	Mycobacterium_virus	6.8e-53	39.8
WP_138966306.1\|2480510_2481302_-	PD-(D/E)XK nuclease family protein	A0A1J0GNS3	Mycobacterium_phage	2.5e-44	39.7

DBSCAN-SWA_3

4766473 : 4807385

Streptomyces_phage(95.35%)

capsid,terminase,portal

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138960574.1\|4766473_4768123_-	long-chain-fatty-acid--CoA ligase	A0A2H4PQU7	Staphylococcus_phage	8.3e-18	23.2
WP_138960575.1\|4768198_4769851_-	recombinase family protein	A0A1J0MCY2	Streptomyces_phage	4.6e-133	48.8
WP_138960576.1\|4769847_4770213_-	hypothetical protein	A0A1V0E644	Streptomyces_phage	2.5e-36	66.1
WP_138960577.1\|4770228_4770678_-	helix-turn-helix domain-containing protein	A0A1V0E635	Streptomyces_phage	1.5e-54	73.3
WP_138960578.1\|4771144_4771339_+	hypothetical protein	A0A1V0E670	Streptomyces_phage	1.5e-16	79.7
WP_138966755.1\|4771403_4771760_+	hypothetical protein	A0A1V0E656	Streptomyces_phage	6.1e-35	65.9
WP_138960579.1\|4771756_4772137_+	hypothetical protein	A0A1J0MC56	Streptomyces_phage	6.7e-32	64.5
WP_138960580.1\|4772133_4773375_+	recombinase RecT	A0A1V0E653	Streptomyces_phage	3.7e-143	72.1
WP_138960581.1\|4773371_4774004_+	hypothetical protein	A0A1V0E652	Streptomyces_phage	2.7e-78	72.6
WP_138960582.1\|4774225_4775188_+	mucin-2	A0A1J0MCR8	Streptomyces_phage	2.1e-130	77.5
WP_138960583.1\|4775184_4775865_+	cell surface glycoprotein	A0A1J0MCX6	Streptomyces_phage	3.2e-77	65.7
WP_138960584.1\|4775861_4776407_+	hypothetical protein	A0A1V0E642	Streptomyces_phage	2.4e-67	73.1
WP_171075798.1\|4776403_4776574_+	hypothetical protein	A0A1J0MD79	Streptomyces_phage	2.4e-13	78.6
WP_138960585.1\|4776694_4777210_+	HNH endonuclease	A0A1J0MCN4	Streptomyces_phage	9.1e-64	85.7
WP_138960586.1\|4777209_4777701_+	single-stranded DNA-binding protein	A0A1J0MC80	Streptomyces_phage	2.1e-65	77.9
WP_171075582.1\|4777787_4777964_+	hypothetical protein	NA	NA	NA	NA
WP_138960587.1\|4777992_4778418_+	hypothetical protein	A0A1V0E663	Streptomyces_phage	6.4e-47	77.5
WP_138960588.1\|4778617_4779625_+	hypothetical protein	A0A1V0E662	Streptomyces_phage	4.7e-32	43.4
WP_138960589.1\|4779621_4780449_+	hypothetical protein	A0A1V0E674	Streptomyces_phage	3.2e-127	83.6
WP_138960590.1\|4780721_4782539_+	hypothetical protein	A0A1J0MCL2	Streptomyces_phage	1.1e-71	36.1
WP_138960591.1\|4782601_4783420_+	hypothetical protein	A0A1J0MCP3	Streptomyces_phage	3.6e-30	50.3
WP_138960592.1\|4783498_4783930_+	hypothetical protein	A0A1J0MCJ1	Streptomyces_phage	1.2e-24	59.0
WP_138960593.1\|4784087_4784621_+	helix-turn-helix domain-containing protein	A0A1J0MC31	Streptomyces_phage	6.7e-62	72.9
WP_138960594.1\|4784625_4785879_+\|terminase	PBSX family phage terminase large subunit	A0A1J0MCH4	Streptomyces_phage	6.8e-214	87.3
WP_138960595.1\|4785847_4786291_-	hypothetical protein	NA	NA	NA	NA
WP_138960596.1\|4786333_4787818_+\|portal	phage portal protein	A0A1J0MCN7	Streptomyces_phage	2.5e-231	79.6
WP_138966757.1\|4787854_4790056_+\|capsid	phage capsid protein	A0A1V0E608	Streptomyces_phage	3.9e-265	69.2
WP_138960597.1\|4790064_4790244_+	hypothetical protein	A0A1J0MC96	Streptomyces_phage	5.1e-14	63.3
WP_138960598.1\|4790357_4791083_+	hypothetical protein	A0A1J0MD42	Streptomyces_phage	3.7e-47	50.8
WP_138960599.1\|4791103_4792114_+\|capsid	phage capsid protein	A0A1J0MCK3	Streptomyces_phage	3.2e-89	55.5
WP_138960600.1\|4792125_4792371_+	hypothetical protein	NA	NA	NA	NA
WP_138960601.1\|4792375_4792765_+	hypothetical protein	A0A1J0MCI1	Streptomyces_phage	4.2e-53	81.4
WP_138960602.1\|4792761_4793079_+	hypothetical protein	A0A1J0MC76	Streptomyces_phage	7.8e-34	70.8
WP_138960603.1\|4793075_4793426_+	hypothetical protein	A0A1V0E617	Streptomyces_phage	7.1e-44	82.8
WP_138960604.1\|4793422_4793854_+	hypothetical protein	A0A1J0MC59	Streptomyces_phage	2.5e-14	38.4
WP_138960605.1\|4793865_4794411_+	hypothetical protein	NA	NA	NA	NA
WP_138960606.1\|4794410_4794881_+	hypothetical protein	NA	NA	NA	NA
WP_138960607.1\|4795126_4797184_+	hypothetical protein	A0A1V0E632	Streptomyces_phage	2.5e-27	61.5
WP_138960608.1\|4797205_4799350_+	hypothetical protein	A0A142K644	Streptomyces_phage	1.3e-82	34.7
WP_138966761.1\|4799397_4800999_+	right-handed parallel beta-helix repeat-containing protein	D7NW65	Streptomyces_phage	3.5e-138	50.2
WP_138960609.1\|4802518_4803445_+	N-acetylmuramoyl-L-alanine amidase	A0A0K1Y5X7	Streptomyces_phage	1.8e-78	67.8
WP_138960610.1\|4803498_4803735_+	hypothetical protein	A0A1J0MD62	Streptomyces_phage	8.4e-25	83.3
WP_138960611.1\|4803731_4803995_+	hypothetical protein	A0A1J0MCF7	Streptomyces_phage	1.0e-34	90.4
WP_138960612.1\|4804055_4805408_-	transcriptional regulator	A0A1J0MD11	Streptomyces_phage	1.3e-215	83.6
WP_138960613.1\|4805566_4806001_+	ATP-binding protein	A0A1V0E640	Streptomyces_phage	4.2e-46	66.7
WP_138960614.1\|4805979_4806480_+	hypothetical protein	A0A1J0MCS0	Streptomyces_phage	9.1e-53	63.4
WP_171075799.1\|4806620_4806794_+	hypothetical protein	A0A1J0MCJ2	Streptomyces_phage	7.6e-15	63.2
WP_171075800.1\|4806938_4807385_+	NUDIX hydrolase	D0R7I2	Paenibacillus_phage	8.3e-05	39.1

DBSCAN-SWA_4

8978999 : 9001940

Streptomyces_phage(58.82%)

head,terminase,capsid,tail,portal,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138964143.1\|8978999_8979440_-	hypothetical protein	Q6VY36	Streptomyces_phage	8.0e-53	65.7
WP_138964145.1\|8979439_8979622_-	hypothetical protein	NA	NA	NA	NA
WP_138964147.1\|8979631_8980420_-	N-acetylmuramoyl-L-alanine amidase	A0A0K1Y5X7	Streptomyces_phage	6.6e-98	64.4
WP_138964149.1\|8980419_8980656_-	hypothetical protein	A0A1D8EVF2	Mycobacterium_phage	3.6e-15	56.8
WP_171075964.1\|8980718_8983364_-	right-handed parallel beta-helix repeat-containing protein	A0A0K1Y5U2	Streptomyces_phage	3.3e-141	42.4
WP_138964151.1\|8983376_8983994_-	hypothetical protein	A0A0K1Y5B7	Streptomyces_phage	3.2e-71	63.7
WP_138967480.1\|8984005_8984920_-	hypothetical protein	A0A0K1Y5A0	Streptomyces_phage	4.1e-99	61.3
WP_138964153.1\|8984934_8986092_-\|tail	phage tail protein	A0A0K1Y599	Streptomyces_phage	1.3e-115	56.6
WP_138964155.1\|8986091_8986970_-	hypothetical protein	A0A0K1Y5X3	Streptomyces_phage	3.8e-70	50.3
WP_138964157.1\|8986990_8991364_-\|tail	phage tail tape measure protein	A0A0K1Y580	Streptomyces_phage	6.7e-224	51.4
WP_138967482.1\|8991386_8991761_-	hypothetical protein	NA	NA	NA	NA
WP_138964159.1\|8991808_8992174_-	hypothetical protein	Q6VY44	Streptomyces_phage	6.9e-26	55.8
WP_138964161.1\|8992178_8992544_-	hypothetical protein	NA	NA	NA	NA
WP_138964163.1\|8992629_8993400_-	Ig-like domain-containing protein	A0A2H4PA05	Gordonia_phage	4.7e-24	37.3
WP_138967484.1\|8993462_8993882_-	DUF3168 domain-containing protein	NA	NA	NA	NA
WP_138964165.1\|8993878_8994160_-	hypothetical protein	A0A2H4P9V4	Gordonia_phage	2.4e-10	48.8
WP_138964167.1\|8994169_8994538_-	hypothetical protein	A0A2P1JSY3	Streptomyces_phage	1.8e-18	44.2
WP_138964169.1\|8994554_8995112_-	mobile element protein	NA	NA	NA	NA
WP_138964171.1\|8995104_8995410_-	hypothetical protein	NA	NA	NA	NA
WP_138964173.1\|8995496_8995709_-	hypothetical protein	NA	NA	NA	NA
WP_138964175.1\|8995724_8997053_-\|capsid	phage major capsid protein	A0A222ZEN6	Arthrobacter_phage	1.4e-76	40.0
WP_138967486.1\|8997059_8997950_-\|head,protease	HK97 family phage prohead protease	A0A222ZEN8	Arthrobacter_phage	3.4e-42	47.3
WP_138964177.1\|8997963_8999922_-\|portal	phage portal protein	A0A222ZFM5	Arthrobacter_phage	2.5e-122	41.0
WP_138964179.1\|8999921_9000140_-	hypothetical protein	NA	NA	NA	NA
WP_138964181.1\|9000161_9001940_-\|terminase	terminase large subunit	A0A1B3B1U6	Gordonia_phage	1.4e-196	58.7

DBSCAN-SWA_5

9019445 : 9025616

Streptomyces_phage(71.43%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138964250.1\|9019445_9020135_-	VWA domain-containing protein	A0A160DF64	Gordonia_phage	2.1e-31	37.7
WP_138964252.1\|9020198_9020447_-	hypothetical protein	NA	NA	NA	NA
WP_138964254.1\|9020443_9020683_-	hypothetical protein	NA	NA	NA	NA
WP_138964256.1\|9020679_9020979_-	WhiB family transcriptional regulator	NA	NA	NA	NA
WP_138964258.1\|9020975_9021533_-	hypothetical protein	A0A0M4QTU3	Streptomyces_phage	8.7e-36	47.0
WP_138967490.1\|9021544_9022168_-	hypothetical protein	Q1WDI4	Streptomyces_phage	3.1e-34	49.1
WP_138964260.1\|9022358_9023162_-	DNA polymerase III subunit epsilon	Q1WDI5	Streptomyces_phage	3.8e-32	35.7
WP_138967492.1\|9023185_9023632_-	HNH endonuclease	G9FH70	Rhodococcus_phage	5.1e-23	42.9
WP_138964262.1\|9023757_9024783_-	hypothetical protein	Q6VY80	Streptomyces_phage	4.4e-86	50.1
WP_138964264.1\|9024782_9025616_-	hypothetical protein	Q6VY81	Streptomyces_phage	1.2e-76	54.7

DBSCAN-SWA_6

9069162 : 9078199

Streptomyces_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_171075974.1\|9069162_9069741_+	TerD family protein	A0A1J0GW82	Streptomyces_phage	9.0e-28	37.8
WP_138964379.1\|9069902_9070535_+	hypothetical protein	A0A2D1GGF9	Gordonia_phage	4.9e-19	37.2
WP_138964381.1\|9070531_9071398_+	PD-(D/E)XK nuclease-like domain-containing protein	A0A0R8VB90	Thermobifida_phage	1.5e-58	44.7
WP_138964383.1\|9071394_9072258_+	hypothetical protein	A0A1B3B1U8	Gordonia_phage	7.3e-66	51.2
WP_138964385.1\|9072337_9072709_+	hypothetical protein	NA	NA	NA	NA
WP_138964387.1\|9072705_9073083_+	DUF2493 domain-containing protein	A0A1I9SDK9	Streptomyces_phage	4.3e-23	50.8
WP_138964389.1\|9073183_9073441_+	hypothetical protein	NA	NA	NA	NA
WP_138964391.1\|9073437_9073833_+	hypothetical protein	NA	NA	NA	NA
WP_138964393.1\|9073829_9074252_+	hypothetical protein	NA	NA	NA	NA
WP_138964395.1\|9074248_9075271_+	DNA cytosine methyltransferase	A5YK40	Mycobacterium_phage	5.8e-54	38.7
WP_138964397.1\|9075385_9076234_+	hypothetical protein	R4JHP8	Mycobacterium_phage	3.2e-42	37.1
WP_138964399.1\|9076307_9077459_+	HNH endonuclease	I6RTT8	Marinomonas_phage	1.4e-11	36.4
WP_138964401.1\|9077455_9078199_+	hypothetical protein	Q6VY73	Streptomyces_phage	1.6e-37	43.8

DBSCAN-SWA_7

9117878 : 9124526

Mycobacterium_phage(33.33%)

capsid,terminase,portal

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_171075985.1\|9117878_9118043_+	HNH endonuclease	A0A1C9M094	Mycobacterium_phage	4.2e-07	59.1
WP_138964525.1\|9118415_9118904_+	hypothetical protein	Q6VY56	Streptomyces_phage	1.2e-57	67.9
WP_138964527.1\|9118908_9120585_+\|terminase	terminase	A0A0K1Y5V8	Streptomyces_phage	2.3e-188	58.8
WP_138964529.1\|9120581_9122051_+\|portal	phage portal protein	A0A2H4JAT8	uncultured_Caudovirales_phage	2.5e-74	41.8
WP_138964531.1\|9122028_9122847_+	hypothetical protein	F8S0R5	Gordonia_phage	3.1e-05	31.3
WP_138964533.1\|9122910_9123546_+	hypothetical protein	NA	NA	NA	NA
WP_138964535.1\|9123566_9124526_+\|capsid	phage major capsid protein	A0A127KPY1	Mycobacterium_phage	2.3e-20	29.3

Anti-CRISPR protein detection

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

2. NZ_CP030772

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

143875 : 289534

108

Enterobacteria_phage(20.0%)

transposase,plate,integrase,tail

attL 155555:155571|attR 274659:274701

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138958190.1\|143875_145546_-\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_138967843.1\|146017_146794_-	aldo/keto reductase	NA	NA	NA	NA
WP_138968754.1\|146790_147357_-	AAA family ATPase	NA	NA	NA	NA
WP_138967845.1\|147380_147983_-	3'-5' exonuclease	NA	NA	NA	NA
WP_138967847.1\|147979_149167_-	radical SAM protein	NA	NA	NA	NA
WP_138967849.1\|149166_150228_-	nucleoside-diphosphate kinase	D2E8E1	Anguillid_herpesvirus	9.4e-07	29.9
WP_138967851.1\|150224_151241_-	thymidylate synthase	NA	NA	NA	NA
WP_138967853.1\|151750_153922_-	hypothetical protein	NA	NA	NA	NA
WP_138968756.1\|153918_154119_-	hypothetical protein	NA	NA	NA	NA
WP_138968758.1\|154201_154819_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_138967855.1\|154821_155046_-	hypothetical protein	NA	NA	NA	NA
WP_138967857.1\|155237_155723_-	hypothetical protein	NA	NA	NA	NA
155555:155571	attL	NA	NA	NA	NA
WP_138968760.1\|156303_157395_+	XRE family transcriptional regulator	NA	NA	NA	NA
155555:155571	attL	NA	NA	NA	NA
WP_138967859.1\|157428_158334_+	phosphotransferase	NA	NA	NA	NA
WP_138968762.1\|159505_160339_+	conjugal transfer protein	NA	NA	NA	NA
WP_138967861.1\|160338_160665_+	hypothetical protein	NA	NA	NA	NA
WP_171076184.1\|160661_161240_+	hypothetical protein	NA	NA	NA	NA
WP_138967863.1\|161239_163924_+	ATP-binding protein	NA	NA	NA	NA
WP_138967865.1\|163920_164259_+	hypothetical protein	NA	NA	NA	NA
WP_138967867.1\|164264_166967_+	hypothetical protein	NA	NA	NA	NA
WP_138967869.1\|166963_168151_+	C40 family peptidase	A0A1J0GW44	Streptomyces_phage	7.8e-10	33.6
WP_138968766.1\|168510_168810_+	hypothetical protein	NA	NA	NA	NA
WP_138967871.1\|169264_169753_+	hypothetical protein	NA	NA	NA	NA
WP_138968768.1\|169992_170649_+	ATP/GTP-binding protein	NA	NA	NA	NA
WP_138967873.1\|170676_171363_+	hypothetical protein	NA	NA	NA	NA
WP_138968770.1\|171374_172280_+	hypothetical protein	NA	NA	NA	NA
WP_138967875.1\|172392_173793_+	Flp pilus assembly complex ATPase component TadA	NA	NA	NA	NA
WP_138967877.1\|173789_174749_+	type II secretion system F family protein	NA	NA	NA	NA
WP_138968772.1\|174739_175648_+	hypothetical protein	NA	NA	NA	NA
WP_138967879.1\|175692_175914_+	hypothetical protein	NA	NA	NA	NA
WP_138967881.1\|175910_176324_+	pilus assembly protein	NA	NA	NA	NA
WP_138968774.1\|176410_176836_+	hypothetical protein	NA	NA	NA	NA
WP_138967883.1\|176835_177312_+	hypothetical protein	NA	NA	NA	NA
WP_138967885.1\|177314_180746_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_138967887.1\|181084_181366_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_171076185.1\|181503_181656_+	hypothetical protein	NA	NA	NA	NA
WP_138967889.1\|181821_182373_-	flavoprotein	NA	NA	NA	NA
WP_138967891.1\|182369_183617_-	helix-turn-helix transcriptional regulator	A0A0M4RQ74	Streptomyces_phage	4.8e-18	26.7
WP_138967893.1\|183695_184202_+	hypothetical protein	NA	NA	NA	NA
WP_138967895.1\|184198_184591_+	restriction endonuclease	NA	NA	NA	NA
WP_138967897.1\|184870_186073_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138967899.1\|186542_186890_-	hypothetical protein	NA	NA	NA	NA
WP_138967901.1\|186978_187248_+	hypothetical protein	NA	NA	NA	NA
WP_138967903.1\|187551_188460_-\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_138967905.1\|188475_188889_-	hypothetical protein	NA	NA	NA	NA
WP_138967907.1\|188888_189830_-	hypothetical protein	NA	NA	NA	NA
WP_138967909.1\|190111_191818_-\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_138967911.1\|191945_192689_-\|transposase	transposase	NA	NA	NA	NA
WP_138968776.1\|193677_194904_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138967913.1\|195038_197141_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138967915.1\|197103_198495_+\|transposase	IS21 family transposase	A0A2L1IVA1	Escherichia_phage	3.0e-21	29.2
197349:197365	attR	NA	NA	NA	NA
WP_138967917.1\|198494_199019_+	ATP-binding protein	NA	NA	NA	NA
197349:197365	attR	NA	NA	NA	NA
WP_138967919.1\|199269_200430_+	hypothetical protein	NA	NA	NA	NA
WP_138967921.1\|200426_200918_+	hypothetical protein	NA	NA	NA	NA
WP_138967923.1\|200914_202867_+	DUF3732 domain-containing protein	NA	NA	NA	NA
WP_138967925.1\|202906_203323_-	hypothetical protein	NA	NA	NA	NA
WP_138967927.1\|203322_205620_-	hypothetical protein	NA	NA	NA	NA
WP_138967929.1\|205616_207395_-	hypothetical protein	NA	NA	NA	NA
WP_138967931.1\|207553_209014_-\|integrase	site-specific integrase	NA	NA	NA	NA
WP_138967933.1\|209148_209562_+	ATP-binding protein	U5N3V8	Enterobacteria_phage	2.9e-28	46.8
WP_138967935.1\|210009_210498_-	hypothetical protein	NA	NA	NA	NA
WP_138967937.1\|211465_211735_+	hypothetical protein	NA	NA	NA	NA
WP_138967939.1\|214803_215178_-\|transposase	transposase family protein	NA	NA	NA	NA
WP_138967941.1\|215642_216287_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_138967943.1\|216235_216526_+\|transposase	transposase	A0A1B3AZF8	Gordonia_phage	1.3e-06	38.3
WP_138967945.1\|216675_216771_+\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_138967947.1\|216786_217026_+	hypothetical protein	NA	NA	NA	NA
WP_138967949.1\|217180_217378_+\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_138967951.1\|217497_218253_+\|transposase	transposase	NA	NA	NA	NA
WP_171076186.1\|219215_220589_+\|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	3.1e-42	32.2
WP_138967957.1\|222229_223870_+\|tail	phage tail sheath subtilisin-like domain-containing protein	J9PVC2	Bacillus_phage	3.2e-38	35.7
WP_138967959.1\|224052_224502_+\|tail	phage tail protein	NA	NA	NA	NA
WP_138967961.1\|224494_224917_+	hypothetical protein	NA	NA	NA	NA
WP_138967964.1\|226383_226836_+\|tail	phage tail protein	NA	NA	NA	NA
WP_138967966.1\|226882_227680_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_171076187.1\|227663_229892_+	VgrG-related protein	NA	NA	NA	NA
WP_138967970.1\|229906_230320_+	GPW/gp25 family protein	A0A0E3F3H3	Synechococcus_phage	8.7e-09	42.9
WP_138967972.1\|230316_233499_+\|plate	baseplate J/gp47 family protein	NA	NA	NA	NA
WP_138967974.1\|233727_234033_-	hypothetical protein	NA	NA	NA	NA
WP_138967976.1\|234145_235213_+	hypothetical protein	NA	NA	NA	NA
WP_138967978.1\|235290_235896_+\|transposase	transposase	NA	NA	NA	NA
WP_138967980.1\|235913_236108_+	hypothetical protein	NA	NA	NA	NA
WP_138967982.1\|236244_238134_+	hypothetical protein	NA	NA	NA	NA
WP_138967984.1\|238423_242671_+	hypothetical protein	NA	NA	NA	NA
WP_138967986.1\|243007_243655_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_138967988.1\|243651_245862_+	AAA family ATPase	A0A0R6PCP6	Moraxella_phage	8.5e-26	32.5
WP_138967990.1\|251174_251930_+\|transposase	transposase	NA	NA	NA	NA
WP_138967996.1\|257961_261753_+	hypothetical protein	NA	NA	NA	NA
WP_138967998.1\|263159_263351_-	hypothetical protein	NA	NA	NA	NA
WP_138968000.1\|263408_263780_-	hypothetical protein	NA	NA	NA	NA
WP_138968002.1\|263856_264306_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_138968779.1\|264591_265038_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	1.0e-18	34.0
WP_138968005.1\|265328_269099_+	hypothetical protein	NA	NA	NA	NA
WP_138968007.1\|269242_270013_-\|transposase	transposase	NA	NA	NA	NA
WP_138968009.1\|270153_270777_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_138968011.1\|272237_272459_+	hypothetical protein	NA	NA	NA	NA
WP_138968002.1\|273477_273927_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_138968781.1\|274211_274658_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	3.5e-19	34.7
WP_138968013.1\|275503_276259_+\|transposase	transposase	NA	NA	NA	NA
WP_138968783.1\|278526_279405_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_138968015.1\|279559_280825_-	cytochrome P450	I6XF76	Cotesia_sesamiae_Mombasa_bracovirus	4.9e-18	26.5
WP_138968017.1\|280924_281917_-	4-hydroxy-3-methylbut-2-enyl diphosphate reductase	NA	NA	NA	NA
WP_138968019.1\|281913_282996_-	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968021.1\|282992_284135_-	flavodoxin-dependent (E)-4-hydroxy-3-methylbut-2-enyl-diphosphate synthase	NA	NA	NA	NA
WP_138968023.1\|284131_286084_-	1-deoxy-D-xylulose-5-phosphate synthase	NA	NA	NA	NA
WP_138968025.1\|287189_287522_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968785.1\|287500_288133_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968789.1\|288307_289534_+\|transposase	IS701 family transposase	NA	NA	NA	NA

DBSCAN-SWA_2

295198 : 372174

Acinetobacter_phage(25.0%)

transposase,integrase

attL 323919:323978|attR 374829:377108

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138968031.1\|295198_296146_-\|transposase	Mu transposase C-terminal domain-containing protein	NA	NA	NA	NA
WP_138968033.1\|296256_296643_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138958190.1\|296840_298511_+\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_138967841.1\|298638_300639_-	hypothetical protein	NA	NA	NA	NA
WP_138968035.1\|300794_301667_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968037.1\|301736_302348_+	hypothetical protein	NA	NA	NA	NA
WP_138968039.1\|302307_302883_-\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_138968041.1\|302903_303332_-	RacP protein	NA	NA	NA	NA
WP_138968043.1\|303444_305094_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138968045.1\|305039_305660_-\|transposase	transposase	NA	NA	NA	NA
WP_138968047.1\|305584_306124_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968049.1\|306170_307064_-	hypothetical protein	NA	NA	NA	NA
WP_138968051.1\|307063_308347_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138968053.1\|308343_309174_-	RacO protein	NA	NA	NA	NA
WP_138968055.1\|309879_310512_-	hypothetical protein	NA	NA	NA	NA
WP_138968057.1\|312094_313123_-	hypothetical protein	NA	NA	NA	NA
WP_171076190.1\|314403_314550_-	hypothetical protein	NA	NA	NA	NA
WP_171076191.1\|315934_316084_+	hypothetical protein	NA	NA	NA	NA
WP_171076192.1\|316080_316401_+\|transposase	transposase	A0A0C5AEA5	Paenibacillus_phage	1.2e-10	36.6
WP_138968063.1\|317783_318692_-	calcium-binding protein	NA	NA	NA	NA
WP_138968065.1\|319041_319233_-	hypothetical protein	NA	NA	NA	NA
WP_138968066.1\|319216_319636_-\|transposase	transposase	NA	NA	NA	NA
WP_138968791.1\|321024_321261_-\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	5.9e-10	45.2
WP_171076193.1\|321270_322371_-\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_138968071.1\|322572_322800_-\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_138968074.1\|322860_323109_-	type II toxin-antitoxin system RelE/ParE family toxin	NA	NA	NA	NA
WP_138968077.1\|323105_323381_-	type II toxin-antitoxin system prevent-host-death family antitoxin	NA	NA	NA	NA
323919:323978	attL	NA	NA	NA	NA
WP_138968080.1\|323949_324273_-	hypothetical protein	NA	NA	NA	NA
WP_138968082.1\|327567_327906_-	hypothetical protein	NA	NA	NA	NA
WP_171076194.1\|328510_328657_-	hypothetical protein	NA	NA	NA	NA
WP_171076195.1\|328662_329511_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968086.1\|330145_331174_-\|transposase	transposase	NA	NA	NA	NA
WP_138968793.1\|333446_334925_-\|transposase	transposase	NA	NA	NA	NA
WP_138968088.1\|335174_335480_-	hypothetical protein	NA	NA	NA	NA
WP_171076196.1\|335568_336036_-\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	2.3e-21	36.2
WP_138968002.1\|336299_336749_-\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_138968092.1\|336860_337679_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_171076197.1\|338586_338742_-	hypothetical protein	NA	NA	NA	NA
WP_171076198.1\|339434_339893_+	recombinase family protein	NA	NA	NA	NA
WP_138968098.1\|340234_341551_-\|transposase	transposase	NA	NA	NA	NA
WP_171076199.1\|341985_342333_-	hypothetical protein	NA	NA	NA	NA
WP_138968100.1\|342584_343862_-\|transposase	transposase	NA	NA	NA	NA
WP_138968795.1\|346692_347574_-	SDR family NAD(P)-dependent oxidoreductase	F2NZ12	Diadromus_pulchellus_ascovirus	3.9e-06	28.0
WP_138968007.1\|347633_348404_+\|transposase	transposase	NA	NA	NA	NA
WP_138968105.1\|348562_351121_-	FAD-dependent monooxygenase	NA	NA	NA	NA
WP_138968107.1\|351117_358428_-	amino acid adenylation domain-containing protein	A0A2K9L3I8	Tupanvirus	5.4e-85	21.7
WP_138968109.1\|358754_359000_-\|transposase	transposase	NA	NA	NA	NA
WP_171076200.1\|359128_360916_-	maturase	NA	NA	NA	NA
WP_171076201.1\|361478_361919_-	HNH endonuclease	NA	NA	NA	NA
WP_138968113.1\|362357_364100_-	group II intron reverse transcriptase/maturase	A0A0U4J920	Pseudomonas_phage	4.6e-83	37.6
WP_138968115.1\|364725_365403_-	hypothetical protein	A0A0U4J920	Pseudomonas_phage	7.8e-31	40.0
WP_138968117.1\|365419_368143_-	recombinase family protein	NA	NA	NA	NA
WP_138968119.1\|368273_368522_-	hypothetical protein	NA	NA	NA	NA
WP_138968121.1\|368778_369075_+\|transposase	transposase	NA	NA	NA	NA
WP_171076202.1\|371064_371520_+\|transposase	transposase domain-containing protein	NA	NA	NA	NA
WP_138968125.1\|371565_372174_+\|transposase	transposase	NA	NA	NA	NA
374829:377108	attR	NA	NA	NA	NA

DBSCAN-SWA_3

377086 : 592079

115

Salmonella_phage(33.33%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_171076203.1\|377086_377659_-\|transposase	transposase	NA	NA	NA	NA
WP_171076204.1\|377585_377882_-\|transposase	transposase domain-containing protein	NA	NA	NA	NA
WP_138968802.1\|378796_379276_+	flavin reductase	NA	NA	NA	NA
WP_138968133.1\|379272_381051_+	tryptophan 7-halogenase	NA	NA	NA	NA
WP_138968789.1\|381224_382451_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968804.1\|382790_383990_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138958190.1\|387352_389023_+\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_138967841.1\|389151_391152_-	hypothetical protein	NA	NA	NA	NA
WP_138968135.1\|393711_394164_-	hypothetical protein	NA	NA	NA	NA
WP_138968137.1\|394414_399196_-	acyltransferase domain-containing protein	NA	NA	NA	NA
WP_171076205.1\|399276_402381_-	SDR family oxidoreductase	NA	NA	NA	NA
WP_171076206.1\|402316_402643_-	SDR family NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_171076207.1\|403927_404293_-	hypothetical protein	NA	NA	NA	NA
WP_138968145.1\|404546_404831_-	hypothetical protein	NA	NA	NA	NA
WP_138968147.1\|407436_407769_+	Lsr2 family protein	A0A160DEV0	Gordonia_phage	2.3e-12	39.8
WP_138968149.1\|411981_412419_+	Uma2 family endonuclease	NA	NA	NA	NA
WP_138968151.1\|412520_413276_+\|transposase	transposase	NA	NA	NA	NA
WP_171076208.1\|414968_415424_-\|transposase	transposase	NA	NA	NA	NA
WP_171076209.1\|416665_418666_-\|transposase	transposase	A0A1B0VCD8	Salmonella_phage	5.2e-22	33.2
WP_138968157.1\|419584_420568_+\|transposase	transposase	NA	NA	NA	NA
WP_171076210.1\|421304_421556_+\|transposase	transposase	NA	NA	NA	NA
WP_171076211.1\|421704_422340_+\|transposase	transposase	NA	NA	NA	NA
WP_138968161.1\|426338_426914_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968163.1\|426910_427426_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968165.1\|428787_429114_+	hypothetical protein	NA	NA	NA	NA
WP_138968167.1\|429721_430276_+	Uma2 family endonuclease	NA	NA	NA	NA
WP_138968169.1\|431126_432302_+	hypothetical protein	NA	NA	NA	NA
WP_138968171.1\|434464_435772_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968163.1\|435914_436430_+	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968161.1\|436426_437002_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968175.1\|437133_438054_+\|transposase	transposase	A0A0M5M147	Mycobacterium_phage	7.6e-53	60.9
WP_138968177.1\|438492_439695_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968179.1\|439813_440572_+\|transposase	transposase	NA	NA	NA	NA
WP_138968181.1\|442097_443591_+\|protease	trypsin-like serine protease	NA	NA	NA	NA
WP_138968183.1\|445374_446037_-\|transposase	transposase	NA	NA	NA	NA
WP_138968187.1\|448912_449377_-	hypothetical protein	NA	NA	NA	NA
WP_138968189.1\|449764_449971_+\|transposase	transposase	NA	NA	NA	NA
WP_138968191.1\|450052_450418_+\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_138968193.1\|450407_451844_+\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	9.1e-29	30.3
WP_138968195.1\|452323_452626_+	hypothetical protein	NA	NA	NA	NA
WP_138968198.1\|452622_453636_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968200.1\|453645_454014_+	hypothetical protein	NA	NA	NA	NA
WP_138968202.1\|454010_455144_+	hypothetical protein	NA	NA	NA	NA
WP_138968204.1\|458026_458566_+\|transposase	transposase	NA	NA	NA	NA
WP_138968206.1\|459138_460581_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968809.1\|460640_461255_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968208.1\|461251_461737_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_171076212.1\|461955_463347_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_138968213.1\|464452_465325_+	hypothetical protein	NA	NA	NA	NA
WP_138968811.1\|467132_469283_+	recombinase family protein	A0A0K1Y9M7	Streptomyces_phage	1.5e-06	27.3
WP_171076213.1\|473803_473968_-	hypothetical protein	NA	NA	NA	NA
WP_138968218.1\|474038_474551_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968220.1\|474728_474998_-	hypothetical protein	NA	NA	NA	NA
WP_138968814.1\|476022_476988_+	TniB family NTP-binding protein	NA	NA	NA	NA
WP_138968222.1\|476984_477911_+	TniQ family protein	NA	NA	NA	NA
WP_138968816.1\|480769_481090_-\|transposase	transposase	NA	NA	NA	NA
WP_171076214.1\|481139_481286_+	hypothetical protein	NA	NA	NA	NA
WP_138967903.1\|481634_482543_-\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_138967905.1\|482558_482972_-	hypothetical protein	NA	NA	NA	NA
WP_138967907.1\|482971_483913_-	hypothetical protein	NA	NA	NA	NA
WP_138968226.1\|484128_490389_-	SDR family NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_171076215.1\|490385_491198_-	acyltransferase domain-containing protein	NA	NA	NA	NA
WP_138968230.1\|491248_492010_-	enoyl-CoA hydratase/isomerase family protein	NA	NA	NA	NA
WP_138968232.1\|492006_492759_-	enoyl-CoA hydratase/isomerase family protein	NA	NA	NA	NA
WP_138968234.1\|492751_493987_-	hydroxymethylglutaryl-CoA synthase family protein	NA	NA	NA	NA
WP_138968236.1\|493997_495257_-	polyketide beta-ketoacyl:ACP synthase	NA	NA	NA	NA
WP_138968238.1\|495264_495516_-	acyl carrier protein	NA	NA	NA	NA
WP_171076216.1\|495512_497216_-	polyketide synthase	NA	NA	NA	NA
WP_171076217.1\|498517_498778_+\|transposase	transposase	NA	NA	NA	NA
WP_138968244.1\|498807_500024_-\|transposase	IS3 family transposase	A0A160DCU2	Gordonia_phage	1.5e-40	33.1
WP_171076218.1\|500712_501297_+	hypothetical protein	NA	NA	NA	NA
WP_138968248.1\|502646_502925_+	hypothetical protein	NA	NA	NA	NA
WP_138968250.1\|503712_506940_-\|transposase	Tn3 family transposase	NA	NA	NA	NA
WP_138968818.1\|508289_508838_+	hypothetical protein	NA	NA	NA	NA
WP_138968252.1\|508906_510439_+\|transposase	ISKra4 family transposase	NA	NA	NA	NA
WP_138968254.1\|512103_512703_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968163.1\|512837_513353_+	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968161.1\|513349_513925_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_171076219.1\|513878_515075_-\|transposase	ISL3 family transposase	NA	NA	NA	NA
WP_171076220.1\|515079_516441_-\|transposase	ISL3 family transposase	NA	NA	NA	NA
WP_138968821.1\|517399_518653_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968260.1\|518576_519017_-\|transposase	transposase	NA	NA	NA	NA
WP_138968823.1\|519652_528217_+	SDR family NAD(P)-dependent oxidoreductase	D0R7J2	Paenibacillus_phage	9.6e-25	29.6
WP_171076221.1\|528263_533816_+	SDR family NAD(P)-dependent oxidoreductase	D0R7J2	Paenibacillus_phage	4.2e-21	29.0
WP_138968264.1\|533817_537873_+	SDR family NAD(P)-dependent oxidoreductase	D0R7J2	Paenibacillus_phage	2.6e-20	28.1
WP_138968266.1\|537869_540122_+	polyketide synthase	NA	NA	NA	NA
WP_138968268.1\|540816_542388_+	acyl-CoA carboxylase subunit beta	NA	NA	NA	NA
WP_138968271.1\|542874_543624_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_138968825.1\|544133_544637_-\|transposase	transposase	NA	NA	NA	NA
WP_138968273.1\|544629_544860_-	hypothetical protein	NA	NA	NA	NA
WP_138968827.1\|545622_546879_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138958988.1\|549563_550763_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968830.1\|552783_553443_+\|transposase	transposase	NA	NA	NA	NA
WP_138968275.1\|553495_554854_+	PAS domain S-box protein	NA	NA	NA	NA
WP_138968277.1\|555813_558924_+\|transposase	Tn3 family transposase	A0A1B0V7H9	Salmonella_phage	4.5e-49	24.6
WP_138968279.1\|560576_561659_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968281.1\|561655_562630_+	4-hydroxy-3-methylbut-2-enyl diphosphate reductase	NA	NA	NA	NA
WP_138968283.1\|562678_564061_+	cytochrome P450	S4VQU1	Pandoravirus	4.4e-20	29.6
WP_138968285.1\|564598_564907_-	hypothetical protein	NA	NA	NA	NA
WP_138968287.1\|565227_566952_+	hypothetical protein	NA	NA	NA	NA
WP_138968289.1\|567421_568330_-	recombinase family protein	A0A1B0VBM1	Salmonella_phage	2.6e-05	28.1
WP_138958063.1\|568572_569328_-	GAF domain-containing protein	NA	NA	NA	NA
WP_138968291.1\|569329_570058_-	ANTAR domain-containing protein	NA	NA	NA	NA
WP_138968293.1\|570356_572681_-\|transposase	Tn3 family transposase	NA	NA	NA	NA
WP_138968295.1\|573253_573589_+	hypothetical protein	NA	NA	NA	NA
WP_138968297.1\|573751_574666_+	recombinase family protein	A0A1B0VBM1	Salmonella_phage	7.6e-05	27.5
WP_171076222.1\|574662_576501_-	type I polyketide synthase	D0R7J2	Paenibacillus_phage	1.4e-26	32.1
WP_171076223.1\|577184_577361_-	hypothetical protein	NA	NA	NA	NA
WP_138968301.1\|578893_580819_+	2,3-oxidosqualene cyclase	NA	NA	NA	NA
WP_138968303.1\|580881_581691_+	squalene/phytoene synthase family protein	NA	NA	NA	NA
WP_138968305.1\|581678_582965_+	NAD(P)-binding protein	NA	NA	NA	NA
WP_138968307.1\|584734_586468_-	hypothetical protein	NA	NA	NA	NA
WP_138968309.1\|586593_587688_-	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_171076224.1\|588341_588854_-	hypothetical protein	NA	NA	NA	NA
WP_171076225.1\|588875_592079_-\|transposase	Tn3 family transposase	A0A1B0V7H9	Salmonella_phage	2.4e-45	28.0

DBSCAN-SWA_4

595422 : 671083

Streptomyces_phage(25.0%)

transposase,integrase,protease

attL 590714:590732|attR 681496:681514

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
590714:590732	attL	NA	NA	NA	NA
WP_138968317.1\|595422_596535_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_138968177.1\|597208_598411_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968319.1\|598528_598831_-	hypothetical protein	NA	NA	NA	NA
WP_138968322.1\|598966_600376_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_138968324.1\|600874_601378_-	hypothetical protein	NA	NA	NA	NA
WP_138968326.1\|602493_603501_-	hypothetical protein	NA	NA	NA	NA
WP_171076226.1\|603581_604763_-	aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme	NA	NA	NA	NA
WP_138968330.1\|604928_606107_-	glutathione synthetase	NA	NA	NA	NA
WP_138968332.1\|606180_607440_-	ATP-grasp domain-containing protein	NA	NA	NA	NA
WP_138968334.1\|607508_608600_-	hypothetical protein	NA	NA	NA	NA
WP_138968336.1\|609964_610702_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968338.1\|610804_612010_-	hypothetical protein	NA	NA	NA	NA
WP_138968341.1\|612293_612776_-	toxin-antitoxin system, toxin component	NA	NA	NA	NA
WP_138968343.1\|613884_614856_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968345.1\|615182_616019_-	protein-L-isoaspartate O-methyltransferase	A0A1J0MC37	Streptomyces_phage	5.7e-31	36.8
WP_171076227.1\|616198_617446_+\|transposase	ISL3 family transposase	NA	NA	NA	NA
WP_138968349.1\|617518_617803_+	hypothetical protein	NA	NA	NA	NA
WP_138968351.1\|617799_618024_-\|transposase	Tn3 family transposase	Q1MVP5	Enterobacteria_phage	1.1e-10	47.2
WP_138968353.1\|618209_618803_+	hypothetical protein	NA	NA	NA	NA
WP_138968355.1\|618846_621270_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138968834.1\|621266_622421_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138968359.1\|623998_624907_+	cytochrome P450	NA	NA	NA	NA
WP_138968361.1\|624927_626154_+	cytochrome P450	NA	NA	NA	NA
WP_138968836.1\|626235_627000_+	class II aldolase/adducin family protein	NA	NA	NA	NA
WP_138968363.1\|627601_628552_-	magnesium transporter CorA	NA	NA	NA	NA
WP_138968365.1\|628596_628785_-	hypothetical protein	NA	NA	NA	NA
WP_138968367.1\|632199_633396_-	hypothetical protein	NA	NA	NA	NA
WP_138968369.1\|636357_636690_-	antibiotic biosynthesis monooxygenase	NA	NA	NA	NA
WP_138968371.1\|636747_636954_-	DUF2180 family protein	NA	NA	NA	NA
WP_138968373.1\|636953_637529_-\|protease	DJ-1/PfpI/YhbO family deglycase/protease	NA	NA	NA	NA
WP_138968375.1\|637650_638181_-	RpiB/LacA/LacB family sugar-phosphate isomerase	NA	NA	NA	NA
WP_138968378.1\|638399_639260_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968380.1\|640516_641725_+\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968382.1\|642972_645405_-	hypothetical protein	NA	NA	NA	NA
WP_138968384.1\|646254_646668_-	hypothetical protein	NA	NA	NA	NA
WP_171076228.1\|647641_647941_+\|transposase	transposase	NA	NA	NA	NA
WP_138968388.1\|647996_648662_+\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	3.4e-31	37.8
WP_138968390.1\|650092_650974_-\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_138968838.1\|650970_651246_-\|transposase	transposase	NA	NA	NA	NA
WP_138968392.1\|651547_652039_-	hypothetical protein	NA	NA	NA	NA
WP_138968394.1\|652614_653526_-	AAA family ATPase	NA	NA	NA	NA
WP_138968396.1\|654354_654972_-\|transposase	transposase	NA	NA	NA	NA
WP_138968398.1\|655278_655467_-	hypothetical protein	Q8W6R2	Burkholderia_virus	4.2e-11	56.7
WP_171076229.1\|655661_656099_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968406.1\|659902_660262_+	hypothetical protein	NA	NA	NA	NA
WP_138968408.1\|660298_660514_+	hypothetical protein	NA	NA	NA	NA
WP_138968411.1\|660561_660756_-	hypothetical protein	NA	NA	NA	NA
WP_138968413.1\|660736_661390_-	hypothetical protein	NA	NA	NA	NA
WP_138968415.1\|661433_661712_-	hypothetical protein	NA	NA	NA	NA
WP_138968840.1\|662071_663379_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968161.1\|663476_664052_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968417.1\|664048_664564_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968419.1\|664617_666063_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_171076261.1\|666135_666932_-\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_171076230.1\|666931_667633_-	DUF4158 domain-containing protein	NA	NA	NA	NA
WP_138968789.1\|668308_669535_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968804.1\|669883_671083_+\|transposase	IS701 family transposase	NA	NA	NA	NA
681496:681514	attR	NA	NA	NA	NA

DBSCAN-SWA_5

687350 : 848251

111

Enterobacteria_phage(30.43%)

transposase,integrase

attL 762131:762173|attR 846511:846553

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138968444.1\|687350_688415_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_171076231.1\|688752_689379_-	aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme	NA	NA	NA	NA
WP_138968448.1\|689710_691222_-	UbiD family decarboxylase	NA	NA	NA	NA
WP_138968450.1\|691913_693401_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_138968452.1\|693439_694987_-	cupin domain-containing protein	NA	NA	NA	NA
WP_138968454.1\|695467_696067_+	cytochrome P450	NA	NA	NA	NA
WP_138968254.1\|699825_700425_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968456.1\|701631_702321_+	hypothetical protein	NA	NA	NA	NA
WP_138968458.1\|702636_702888_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_138968460.1\|703129_703927_-	hypothetical protein	NA	NA	NA	NA
WP_138968462.1\|704254_705493_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968464.1\|707587_707818_-	hypothetical protein	NA	NA	NA	NA
WP_138968466.1\|708727_709288_-	hypothetical protein	NA	NA	NA	NA
WP_138968468.1\|709519_710002_+	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968470.1\|710424_710724_+\|transposase	transposase	NA	NA	NA	NA
WP_138968472.1\|710793_711336_+\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	2.9e-12	34.3
WP_138968474.1\|711694_711877_+	hypothetical protein	NA	NA	NA	NA
WP_138968476.1\|715165_715900_-\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	1.5e-24	30.1
WP_138968477.1\|715904_716345_-\|transposase	transposase	B6ETC4	Enterobacteria_phage	8.1e-05	42.2
WP_171076173.1\|717598_717763_+	hypothetical protein	NA	NA	NA	NA
WP_171076232.1\|717853_719485_-	di-trans,poly-cis-decaprenylcistransferase	R9W0U9	Flavobacterium_phage	2.0e-08	36.5
WP_138968481.1\|719474_720548_-	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_138968483.1\|721182_721476_+	recombinase family protein	NA	NA	NA	NA
WP_138968485.1\|722105_722417_-	hypothetical protein	NA	NA	NA	NA
WP_171076233.1\|722625_723582_-\|transposase	transposase	NA	NA	NA	NA
WP_138968472.1\|723880_724423_-\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	2.9e-12	34.3
WP_138968470.1\|724492_724792_-\|transposase	transposase	NA	NA	NA	NA
WP_138968489.1\|726729_727695_-\|transposase	transposase	NA	NA	NA	NA
WP_138968491.1\|727841_728633_+	response regulator	W8CYM9	Bacillus_phage	9.8e-33	34.9
WP_138968493.1\|728629_729865_+	HAMP domain-containing protein	NA	NA	NA	NA
WP_138968789.1\|731044_732271_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_138968495.1\|732874_733348_-	ester cyclase	NA	NA	NA	NA
WP_138968497.1\|733354_734383_-	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_138968499.1\|734459_735266_-	ATP-binding cassette domain-containing protein	G3M9Y6	Bacillus_virus	5.3e-26	33.8
WP_171076234.1\|735348_736221_-	ABC transporter permease	NA	NA	NA	NA
WP_138968503.1\|736217_737603_-	ABC transporter permease subunit	NA	NA	NA	NA
WP_138968505.1\|737654_738722_-	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_171076235.1\|738919_739471_-	flavin reductase family protein	NA	NA	NA	NA
WP_138968509.1\|739581_740376_-	2-oxo acid dehydrogenase subunit E2	NA	NA	NA	NA
WP_138968511.1\|740377_742600_-	MFS transporter	NA	NA	NA	NA
WP_138968513.1\|742700_743207_+	VOC family protein	NA	NA	NA	NA
WP_138968515.1\|743221_744718_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_138968517.1\|744764_746042_-	M24 family metallopeptidase	NA	NA	NA	NA
WP_138968519.1\|746038_747031_-	NAD-binding protein	NA	NA	NA	NA
WP_138968521.1\|747194_748229_+	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_138968523.1\|748222_749269_+	substrate-binding domain-containing protein	C6ZCU4	Enterobacteria_phage	9.0e-26	30.1
WP_138968525.1\|749284_750130_+	cyclic nucleotide-binding domain-containing protein	NA	NA	NA	NA
WP_138968527.1\|750682_751198_+\|transposase	transposase	NA	NA	NA	NA
WP_171076262.1\|751079_751592_-\|transposase	transposase	NA	NA	NA	NA
WP_138968531.1\|751555_752116_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968533.1\|753150_754365_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_171076236.1\|754811_755732_-\|transposase	IS3 family transposase	Q6H9S6	Enterobacteria_phage	5.1e-33	31.7
WP_171076237.1\|756049_756448_-	hypothetical protein	NA	NA	NA	NA
WP_138968025.1\|757048_757381_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968785.1\|757359_757992_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_171076238.1\|757993_758707_-\|transposase	IS3 family transposase	Q8W6R2	Burkholderia_virus	2.3e-09	35.2
WP_138968849.1\|758703_758931_-\|transposase	transposase	NA	NA	NA	NA
WP_138968002.1\|760949_761399_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_171076239.1\|761662_762130_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	7.3e-20	34.9
762131:762173	attL	NA	NA	NA	NA
WP_138968541.1\|762320_763076_+\|transposase	transposase	NA	NA	NA	NA
WP_138968543.1\|763575_764166_+	hypothetical protein	NA	NA	NA	NA
WP_138968080.1\|764382_764706_-	hypothetical protein	NA	NA	NA	NA
WP_138968851.1\|768627_771174_+	phosphotransferase	NA	NA	NA	NA
WP_138968545.1\|771276_771402_+	SapB/AmfS family lantipeptide	NA	NA	NA	NA
WP_138968547.1\|771559_773347_+	ATP-binding cassette domain-containing protein	NA	NA	NA	NA
WP_138968549.1\|773392_775345_+	ATP-binding cassette domain-containing protein	A0A076FI99	Aureococcus_anophage	9.2e-08	26.9
WP_138968551.1\|775289_775979_-	SDR family oxidoreductase	NA	NA	NA	NA
WP_138968121.1\|777360_777657_-\|transposase	transposase	NA	NA	NA	NA
WP_138968553.1\|779022_780066_-	hypothetical protein	NA	NA	NA	NA
WP_171076240.1\|780493_781882_-	cytochrome P450	I6WI04	Cotesia_sesamiae_Mombasa_bracovirus	6.5e-16	29.1
WP_171076241.1\|781857_782274_-	hypothetical protein	NA	NA	NA	NA
WP_138968854.1\|783090_784434_+	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_138968557.1\|784504_785746_-	TniQ family protein	NA	NA	NA	NA
WP_138968220.1\|787703_787973_+	hypothetical protein	NA	NA	NA	NA
WP_138968218.1\|788150_788663_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_171076213.1\|788733_788898_+	hypothetical protein	NA	NA	NA	NA
WP_138968559.1\|791758_792979_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968836.1\|796744_797509_-	class II aldolase/adducin family protein	NA	NA	NA	NA
WP_138968361.1\|797590_798817_-	cytochrome P450	NA	NA	NA	NA
WP_171076242.1\|798837_799608_-	cytochrome P450	NA	NA	NA	NA
WP_171076262.1\|799655_800168_-\|transposase	transposase	NA	NA	NA	NA
WP_138968531.1\|800131_800692_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968252.1\|802453_803986_-\|transposase	ISKra4 family transposase	NA	NA	NA	NA
WP_138968818.1\|804054_804603_-	hypothetical protein	NA	NA	NA	NA
WP_138968563.1\|805487_806042_-	hypothetical protein	NA	NA	NA	NA
WP_171076243.1\|807302_807545_+\|transposase	transposase	NA	NA	NA	NA
WP_138968567.1\|807564_809787_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_171076263.1\|810923_811763_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_138968571.1\|812036_812612_-	hypothetical protein	NA	NA	NA	NA
WP_138968856.1\|813851_815228_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_138968858.1\|815916_816144_+\|transposase	transposase	NA	NA	NA	NA
WP_171076244.1\|816140_816773_+\|transposase	IS3 family transposase	Q8W6R2	Burkholderia_virus	2.1e-09	35.2
WP_171076245.1\|818100_818298_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_138968860.1\|822606_823551_+\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_138968161.1\|824505_825081_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968163.1\|825077_825593_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968577.1\|827472_828285_-	methyltransferase domain-containing protein	A0A1X9I6N4	Streptococcus_phage	1.4e-10	35.7
WP_138968580.1\|828472_829708_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968582.1\|831366_832182_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_138968002.1\|833130_833580_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_138968584.1\|833576_834311_+\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	1.8e-25	30.5
WP_138968586.1\|835073_835346_+	hypothetical protein	NA	NA	NA	NA
WP_171076246.1\|835360_836722_+	cytochrome P450	S4VXU7	Pandoravirus	7.3e-12	25.8
WP_138968864.1\|836772_837495_+	di-trans,poly-cis-decaprenylcistransferase	R9W0U9	Flavobacterium_phage	2.0e-08	31.3
WP_138968591.1\|837662_838679_+	hypothetical protein	NA	NA	NA	NA
WP_171076236.1\|839766_840687_+\|transposase	IS3 family transposase	Q6H9S6	Enterobacteria_phage	5.1e-33	31.7
WP_138968593.1\|841300_842986_+	hypothetical protein	NA	NA	NA	NA
WP_138968596.1\|843063_843276_-	hypothetical protein	NA	NA	NA	NA
WP_138968002.1\|845329_845779_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_171076247.1\|846042_846510_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A0P0I4A4	Acinetobacter_phage	6.0e-22	36.2
WP_138967588.1\|846772_848251_+\|transposase	transposase	NA	NA	NA	NA
846511:846553	attR	NA	NA	NA	NA

DBSCAN-SWA_6

852506 : 922199

Streptomyces_phage(28.57%)

transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_138968606.1\|852506_853376_+\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_138968868.1\|853733_855335_+\|transposase	ISL3 family transposase	NA	NA	NA	NA
WP_138968608.1\|855423_855897_+	hypothetical protein	NA	NA	NA	NA
WP_138968610.1\|856007_856331_+	hypothetical protein	NA	NA	NA	NA
WP_171076249.1\|857380_857557_+	hypothetical protein	NA	NA	NA	NA
WP_138968870.1\|860501_860957_-	hypothetical protein	A0A222YU12	Streptomyces_phage	1.3e-10	56.6
WP_138968614.1\|861527_861809_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968616.1\|863437_863929_-	hypothetical protein	NA	NA	NA	NA
WP_171076250.1\|864122_864959_-	aldo/keto reductase	NA	NA	NA	NA
WP_171076251.1\|865649_865805_-	hypothetical protein	NA	NA	NA	NA
WP_138968621.1\|866328_866784_-	WhiB family transcriptional regulator	NA	NA	NA	NA
WP_171076252.1\|870491_871658_+	PQQ-binding-like beta-propeller repeat protein	NA	NA	NA	NA
WP_138968625.1\|871772_871988_+\|transposase	transposase	A0A0M5M147	Mycobacterium_phage	6.3e-11	55.0
WP_171076253.1\|872290_872626_-\|transposase	transposase	NA	NA	NA	NA
WP_138968629.1\|872622_873690_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968208.1\|873853_874339_+	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968809.1\|874335_874950_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968631.1\|875005_875302_+	hypothetical protein	NA	NA	NA	NA
WP_171076254.1\|875778_875916_+	hypothetical protein	NA	NA	NA	NA
WP_138967937.1\|876267_876537_-	hypothetical protein	NA	NA	NA	NA
WP_138968633.1\|878659_878965_+	hypothetical protein	NA	NA	NA	NA
WP_138968635.1\|880166_880913_-\|transposase	transposase	NA	NA	NA	NA
WP_138968559.1\|883191_884412_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_138968637.1\|884863_885607_+	N-acetylmuramoyl-L-alanine amidase	A0A291LHM6	Streptomyces_phage	6.2e-05	32.5
WP_138968639.1\|885849_886095_+	hypothetical protein	NA	NA	NA	NA
WP_138968809.1\|886277_886892_-\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_138968208.1\|886888_887374_-	winged helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_138968419.1\|887432_888878_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_171076174.1\|889647_889899_+	hypothetical protein	NA	NA	NA	NA
WP_171076255.1\|891926_892136_-	single-stranded DNA-binding protein	A0A0U4B2E8	Arthrobacter_phage	4.8e-16	59.7
WP_138968645.1\|894268_894814_-	Uma2 family endonuclease	NA	NA	NA	NA
WP_171076175.1\|896892_897300_-	hypothetical protein	NA	NA	NA	NA
WP_138968647.1\|897296_897578_-	hypothetical protein	NA	NA	NA	NA
WP_171076256.1\|897632_898844_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_171076257.1\|898891_899299_-	hypothetical protein	NA	NA	NA	NA
WP_171076258.1\|900817_902122_+	hypothetical protein	NA	NA	NA	NA
WP_171076259.1\|903894_904677_+	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_138968872.1\|904660_905755_+	type III polyketide synthase	NA	NA	NA	NA
WP_138968655.1\|905751_906198_+	MaoC family dehydratase	NA	NA	NA	NA
WP_138968657.1\|906201_906702_+	MaoC family dehydratase	NA	NA	NA	NA
WP_138968659.1\|906714_907734_+	methyltransferase	NA	NA	NA	NA
WP_138968661.1\|907851_908301_+\|transposase	transposase	B6ETC4	Enterobacteria_phage	7.3e-09	41.4
WP_138968663.1\|908297_909032_+\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	1.4e-25	30.5
WP_138968665.1\|910104_916491_-	SDR family NAD(P)-dependent oxidoreductase	D0R7J2	Paenibacillus_phage	9.0e-28	32.8
WP_138968874.1\|917265_918246_-	Rieske 2Fe-2S domain-containing protein	NA	NA	NA	NA
WP_138968668.1\|918410_919262_-	Rieske 2Fe-2S domain-containing protein	NA	NA	NA	NA
WP_138968670.1\|919554_919782_-	hypothetical protein	NA	NA	NA	NA
WP_138968876.1\|921989_922199_-\|transposase	transposase family 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_CP030771

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

2. NZ_CP030772

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection