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_CP013859	Microbacterium sp. XT11, complete genome	7 crisprs	csa3,cas3,DEDDh,WYL	1	4	3	0

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP013859_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_1

596994-597102

Orphan

Consensus_repeat	Method
GCACGCGTGAGCCGATCCGCGCGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013859_1

>merge|NZ_CP013859|1|596994-597102|CRISPRCasFinder
GCACGCGTGAGCCGATCCGCGCGCTCCCCGCGCCCGCACGCGTGAACAGATCCGCCCGCTCCCCGCGCCCGCGCCGTCACGCCCGCACGCGTGAGCCGATCCGCGCCTA

>NZ_CP013859|1|1|596994-597102|CRISPRCasFinder
GCACGCGTGAGCCGATCCGCGCGCT	CCCCGCGCCCGCACGCGTGAACAGATCCGCCCGCTCCCCGCGCCCGCGCCGTCACGCCC
GCACGCGTGAGCCGATCCGCGCCTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_157540844.1\|598196_598373_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067195666.1\|592398_593166_+\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP013859.1\|WP_067195703.1\|603469_604282_+\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133381
NZ_CP013859.1\|WP_067195696.1\|602310_602901_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_157540842.1\|586945_587974_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067195690.1\|599105_599570_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235095
NZ_CP013859.1\|WP_067202039.1\|607716_608544_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP013859.1\|WP_067202030.1\|585410_586778_+\|glucose-6-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|237233
NZ_CP013859.1\|WP_067195693.1\|600909_602178_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340844
NZ_CP013859.1\|WP_067195651.1\|581657_582602_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176115
NZ_CP013859.1\|WP_067195659.1\|583535_585332_-\|glycoside-hydrolase-family-15-protein	unknown	unknown	gnl\|CDD\|225922
NZ_CP013859.1\|WP_067195699.1\|602946_603486_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319898
NZ_CP013859.1\|WP_083511068.1\|588428_590636_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|274529
NZ_CP013859.1\|WP_067195677.1\|594937_596164_-\|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	unknown	unknown	gnl\|CDD\|235513
NZ_CP013859.1\|WP_067195655.1\|582788_583376_+\|nitroreductase	unknown	unknown	gnl\|CDD\|380315
NZ_CP013859.1\|WP_157541200.1\|590866_592021_-\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|238640
NZ_CP013859.1\|WP_067202035.1\|599680_600907_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340844
NZ_CP013859.1\|WP_067195648.1\|577990_581524_-\|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143443
NZ_CP013859.1\|WP_067195708.1\|608681_609629_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP013859.1\|WP_067195706.1\|604597_607591_-\|alpha-mannosidase	unknown	unknown	gnl\|CDD\|223460

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_067202035.1\|599680_600907_-\|glycosyltransferase	gnl\|CDD\|340844	cd03817, GT4_UGDG-like, UDP-Glc:1,2-diacylglycerol 3-a-glucosyltransferase and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. UDP-glucose-diacylglycerol glucosyltransferase (EC 2.4.1.337, UGDG; also known as 1,2-diacylglycerol 3-glucosyltransferase) catalyzes the transfer of glucose from UDP-glucose to 1,2-diacylglycerol forming 3-D-glucosyl-1,2-diacylglycerol.	5.36013e-34
NZ_CP013859.1\|WP_067195666.1\|592398_593166_+\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	6.12663e-67
NZ_CP013859.1\|WP_067195706.1\|604597_607591_-\|alpha-mannosidase	gnl\|CDD\|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	4.52491e-137
NZ_CP013859.1\|WP_067195703.1\|603469_604282_+\|MerR-family-transcriptional-regulator	gnl\|CDD\|133381	cd01106, HTH_TipAL-Mta, Helix-Turn-Helix DNA binding domain of the transcription regulators TipAL, Mta, and SkgA. Helix-turn-helix (HTH) TipAL, Mta, and SkgA transcription regulators, and related proteins, N-terminal domain. TipAL regulates resistance to and activation by numerous cyclic thiopeptide antibiotics, such as thiostrepton. Mta is a global transcriptional regulator; the N-terminal DNA-binding domain of Mta interacts directly with the promoters of mta, bmr, blt, and ydfK, and induces transcription of these multidrug-efflux transport genes. SkgA has been shown to control stationary-phase expression of catalase-peroxidase in Caulobacter crescentus. These proteins are comprised of distinct domains that harbor an N-terminal active (DNA-binding) site and a regulatory (effector-binding) site. The conserved N-terminal domain of these transcription regulators contains winged HTH motifs that mediate DNA binding. These proteins share the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements. Unique to this family, is a TipAL-like, lineage specific Bacilli subgroup, which has five conserved cysteines in the C-terminus of the protein.	1.35626e-34
NZ_CP013859.1\|WP_067202030.1\|585410_586778_+\|glucose-6-phosphate-dehydrogenase	gnl\|CDD\|237233	PRK12853, PRK12853, glucose-6-phosphate dehydrogenase.	1.34189e-170
NZ_CP013859.1\|WP_067195690.1\|599105_599570_+\|hypothetical-protein	gnl\|CDD\|235095	PRK02983, lysS, bifunctional lysylphosphatidylglycerol synthetase/lysine--tRNA ligase LysX.	0.00526305
NZ_CP013859.1\|WP_067202039.1\|607716_608544_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.14222e-68
NZ_CP013859.1\|WP_067195699.1\|602946_603486_+\|VOC-family-protein	gnl\|CDD\|319898	cd06587, VOC, vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC is found in a variety of structurally related metalloproteins, including the type I extradiol dioxygenases, glyoxalase I and a group of antibiotic resistance proteins. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). Type I extradiol dioxygenases catalyze the incorporation of both atoms of molecular oxygen into aromatic substrates, which results in the cleavage of aromatic rings. They are key enzymes in the degradation of aromatic compounds. Type I extradiol dioxygenases include class I and class II enzymes. Class I and II enzymes show sequence similarity; the two-domain class II enzymes evolved from a class I enzyme through gene duplication. Glyoxylase I catalyzes the glutathione-dependent inactivation of toxic methylglyoxal, requiring zinc or nickel ions for activity. The antibiotic resistance proteins in this family use a variety of mechanisms to block the function of antibiotics. Bleomycin resistance protein (BLMA) sequesters bleomycin's activity by directly binding to it. Whereas, three types of fosfomycin resistance proteins employ different mechanisms to render fosfomycin inactive by modifying the fosfomycin molecule. Although the proteins in this superfamily are functionally distinct, their structures are similar. The difference among the three dimensional structures of the three types of proteins in this superfamily is interesting from an evolutionary perspective. Both glyoxalase I and BLMA show domain swapping between subunits. However, there is no domain swapping for type 1 extradiol dioxygenases.	9.84824e-07
NZ_CP013859.1\|WP_067195693.1\|600909_602178_-\|glycosyltransferase	gnl\|CDD\|340844	cd03817, GT4_UGDG-like, UDP-Glc:1,2-diacylglycerol 3-a-glucosyltransferase and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. UDP-glucose-diacylglycerol glucosyltransferase (EC 2.4.1.337, UGDG; also known as 1,2-diacylglycerol 3-glucosyltransferase) catalyzes the transfer of glucose from UDP-glucose to 1,2-diacylglycerol forming 3-D-glucosyl-1,2-diacylglycerol.	1.91566e-77
NZ_CP013859.1\|WP_067195651.1\|581657_582602_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|176115	cd08423, PBP2_LTTR_like_6, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator, contains the type 2 periplasmic binding fold. LysR-transcriptional regulators comprise the largest family of prokaryotic transcription factor. Homologs of some of LTTRs with similar domain organizations are also found in the archaea and eukaryotic organisms. The LTTRs are composed of two functional domains joined by a linker helix involved in oligomerization: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal substrate-binding domain, which is structurally homologous to the type 2 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcriptional repressor undergoes a conformational change upon substrate binding which in turn changes the DNA binding affinity of the repressor. The genes controlled by the LTTRs have diverse functional roles including amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to a name a few. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.7925e-38
NZ_CP013859.1\|WP_067195659.1\|583535_585332_-\|glycoside-hydrolase-family-15-protein	gnl\|CDD\|225922	COG3387, SGA1, Glucoamylase and related glycosyl hydrolases [Carbohydrate transport and metabolism].	7.55553e-134
NZ_CP013859.1\|WP_083511068.1\|588428_590636_-\|AAA-domain-containing-protein	gnl\|CDD\|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP013859.1\|WP_067195677.1\|594937_596164_-\|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	gnl\|CDD\|235513	PRK05579, PRK05579, bifunctional phosphopantothenoylcysteine decarboxylase/phosphopantothenate synthase; Validated.	0
NZ_CP013859.1\|WP_067195655.1\|582788_583376_+\|nitroreductase	gnl\|CDD\|380315	cd02138, TdsD-like, nitroreductase similar to Burkholderia pseudomallei TdsD. A subfamily of the nitroreductase family containing uncharacterized proteins that are similar to Burkholderia pseudomallei TdsD, may be involved in the processing of organosulfur compounds. Nitroreductase catalyzes the reduction of nitroaromatic compounds such as nitrotoluenes, nitrofurans and nitroimidazoles. This process requires NAD(P)H as electron donor in an obligatory two-electron transfer and uses FMN as cofactor. The enzyme is typically a homodimer.	7.99627e-72
NZ_CP013859.1\|WP_157541200.1\|590866_592021_-\|amidohydrolase-family-protein	gnl\|CDD\|238640	cd01315, L-HYD_ALN, L-Hydantoinases (L-HYDs) and Allantoinase (ALN); L-Hydantoinases are a member of the dihydropyrimidinase family, which catalyzes the reversible hydrolytic ring opening of dihydropyrimidines and hydantoins (five-membered cyclic diamides used in biotechnology). But L-HYDs differ by having an L-enantio specificity and by lacking activity on possible natural substrates such as dihydropyrimidines. Allantoinase catalyzes the hydrolytic cleavage of the five-member ring of allantoin (5-ureidohydantoin) to form allantoic acid.	1.43269e-119
NZ_CP013859.1\|WP_067195648.1\|577990_581524_-\|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase	gnl\|CDD\|143443	cd07125, ALDH_PutA-P5CDH, Delta(1)-pyrroline-5-carboxylate dehydrogenase, PutA. The proline catabolic enzymes of the aldehyde dehydrogenase (ALDH) protein superfamily, proline dehydrogenase and Delta(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH, (EC=1.5.1.12 )), catalyze the two-step oxidation of proline to glutamate; P5CDH catalyzes the oxidation of glutamate semialdehyde, utilizing NAD+ as the electron acceptor. In some bacteria, the two enzymes are fused into the bifunctional flavoenzyme, proline utilization A (PutA) These enzymes play important roles in cellular redox control, superoxide generation, and apoptosis. In certain prokaryotes such as Escherichia coli, PutA is also a transcriptional repressor of the proline utilization genes.	0
NZ_CP013859.1\|WP_067195708.1\|608681_609629_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.20674e-67

>NZ_CP013859.1|WP_067195677.1|594937_596164_-|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC
MNIVVGVSGGIAAYKSVQLVRLLVKAGHDVTVVPTDDALRFVGAPTWEAISRNPVTTSVHDDVARVRHVALGQGADLIVVAPATANTIARMAAGIADNLLGTTLLASVAPVLIAPAMHTEMWRHPATQANVATLRQRGVHVIGPGEGELAGGDSGPGRMLEPEEIADAALALLAPRDLEGLRVVVSAGGTREPLDPVRYLGNRSSGRQGVAVAAEAALRGADVTLVAANVAGDVLQAARHPSLRVVHAGSAAELGAVMRTEAQGADVVVMAAAVADYRPATVSDRKLTKESGGVTAIELVENEDIVAGLARDRAPGTTVVAFAAETPRSDEELLERARRKQQRKGVDLLVVNEVGWERGFESAENAVRILGRDGAVVASVDGSKRAVAAALWDAVADAVTADAEHDAH
>NZ_CP013859.1|WP_067195666.1|592398_593166_+|IclR-family-transcriptional-regulator
MAESRTPKSAGSGVQSVERVFELLELVTDAGGDVTLSELAASTDLPLPTIHRLLRTLVSLGYARQLPNRRYALGPRLIRIGEGASRQFGALARPQLKGLVDALGESANMAVLDGDMVVYVAQVPSQHSMRMFTEVGRRAHLHDTGVGKAILAQLPDETVRGIVSRAGMPTPTEFSIGTVHALLAELEVIRERGYAIDDQEQEIGVRCFSMAIPGAPTPTAVSVSGPVSRVDEQFGERAVPLLRRAAEAISAELAS
>NZ_CP013859.1|WP_157541200.1|590866_592021_-|amidohydrolase-family-protein
MYLGRSYSVVTTLDRTVPLIEDRLILAGLHDRCASVRSSGLGVLELESDPERAVEAIAAEAQRAVEVDRAEVIVLGCGGMAELKDRVVELCGVPVVDEFPPLDADELEEDMRELASFDSVMIVHAEDSRAIDRAPQPEGDDYGKFLASRPRGAENLAIAEVIERARWTGARAHILHLSSSDALPMLRTAKQDGLKLTVETCPHYLTLTAEEIPHGATQFKCCPPIREAGNRELLWQGLEDGTIDFIVSDHSPSTLDLKDLENGDFAVAWGGVASLQLGLSLIWTEARQRGLSLETVVGWMSERPAQFAGLTGKGRIAPGYDADFSVFAADDAYVVDVAKLHHKNPLTPYHGKALAGVVRKTWLHGEVVDFETPRGRLLRRGMTE
>NZ_CP013859.1|WP_083511068.1|588428_590636_-|AAA-domain-containing-protein
MTTPQTSPQSEEQQSALEQFGINLTDRARQGKLDPVIGRDSEIRRVSQVLTRRTKNNPVLIGEPGVGKTAVVEGLAQRIVAGDVAESLKDKELVSLDISALVAGAMYRGQFEERLKSVLKEITESDGRIITFIDELHVLMGAGGGEGSVAASNMLKPMLARGELRLIGATTLNEYREFIEKDAALERRFQQVYVGEPSVEDTIAILRGLKGRYEAHHGVTISDSALVAAAALSNRYLPARQLPDKAIDLVDESMSRLKMEIDSSPVEIDQLKRQVDRMKLEELALKKEKDDASKERLSTLREQLVVQEKELAELEARWARERQGLNRVGELKKQLDDAITQRDLAMRNADYTTASKLEYETIKRLERDIAEAEQAEAAASTEGRMVNEQVTEEDIAAVIAAWTGIPVGRLLQGESEKLLHLESELGKRLIGQKEAVKAVSDAVRRSRAGISDPGRPTGSFLFLGPTGVGKTELAKALAEFLFDDERAMVRIDMSEYGEKHSVSRLVGAPPGYIGYEQGGQLTEAVRRRPYSVVLLDEVEKAHPEVFDVLLQVLDDGRLTDGQGRTVDFSNVILVLTSNIGSPILIDPVLSPDEKREQVMALVRQAFRPEFLNRLDDIVMFQALSEDDLAQIVELSIDQLQKRLHERRLTLGVTPDARSWLAERGYDPVFGARPLRRLIQTEVQNRLATALLSGGVRDGDTVRVDVAADGTGLVLTSEGPAPQLDDDVIEAELLDD
>NZ_CP013859.1|WP_157540842.1|586945_587974_+|hypothetical-protein
MLWPVLTLTFGSLPFVVVLVLSTGRQPVISDYWSTVAGLGGWLSPAFTNGFSAIQTVGMVLVAVAAFTGLAGDWQSVPPRARRFIRPLAGVCTVTIGAMGALTPLAVVHSPATASTAVLLWMCCWAVMLFGLGVSEIAPLRRRMIFARARHVRALRLLERDPLPAAPTRPELVLAVVAICVIPVVVTYAACGLVALMLGSLWPLQPAMLLLSYSGYVAHLGWLIRADRTQSTAYRRLGGFIVLIGGAIGVLFGLPLLAIPPAGFAFIILGLLTAVVLLLPRITTRLWPYRVISAYATNRGKTAIDEQAARLFTWWKDEVKRSVAARPRQGLRARLAAWLTAP
>NZ_CP013859.1|WP_067202030.1|585410_586778_+|glucose-6-phosphate-dehydrogenase
MTSTPTTLFILGASGDLTSRLLLPSLAALLQRQPQRRIAVRGAGTEAWDASTWRSVVSDAFTDAPDALDRVHIEDYVAADVTDRTAVASLVESLAPGTVLYFALPPAVTRAAIEAMQGLTLPEGTLLAMEKPFGDDEASARELNERLLALVPEQQVFRVDHFLGRSTLLNLLGVRLPHRIWEPVWSAEHIESVFIRFDESLALEGRARYYDKAGAMIDMIQSHLLQVLALLAMDPPASLDERDLRDAKAAVLRATHVRGDDPAASSRRARYTAGRVGDRELPAYVDEEGVDAARNTETLAEVTFEVSNDRWEGVPFVLRSGKALRAKHSEVVVTFRQVRHLPRGLAGQPADGGRLTFSLGPDTMVLGLHVTGGDDPFALRDEDLTADLGEGQRRSYEEALDELLDGEVALSVRADEAEECWRIIQPVRDAWAKGEVPLEEYAAGSLGPASWPTSN
>NZ_CP013859.1|WP_067195659.1|583535_585332_-|glycoside-hydrolase-family-15-protein
MAARIEDYALLSNCRTAALVSTTGSIDWLCLPRLDSPSVFGALLGDEAHGRWQLRPADPDAICTRRYDGDTFVLITRWESADAVAEVHDFMPIGLDPDVAIRRTDLVRRIIGVQGEMRFAQRLSIRFDYSRGMPWVRQTGTESHPCLVAMGGPDAVAVRGARLTAADHRHEGELTVRAGEVRNLHLTWFPSHRDVPPELDTDDELEQTKSWWQEWADRISHDGPRRGDVVRSLLILRALTNHETGGIAAAATMALPEEIGGERNWDYRYVWLRDAALTLEALLDHGFLVVADRWREWLLRAVAGDPGDLQIMYGLAGERDLLERELPAFPGYEGSRPVRIGNGAAAQYQADVVGEVLVTLSAARSAGLDESEFSWPLERQLVRFASEQIERPDQGLWEIRGEPHHFTHSRVMMWAAFDRAVRGVEEFGLEGPVDRWRGLRDRMREEIDTRGVVDGHFVQYYGTNEVDASLLLLPQVGYCEPGDPRMLATVDRIEQTLMRDGLVRRYRTGTGVDGLSGTEGAFLACSFWLVEQYALTGRREEAHALMDRLCGLANDVGMLSEEYDTVAGRQLGNTPQAFSHLALVRAADALTRTAHRPR
>NZ_CP013859.1|WP_067195655.1|582788_583376_+|nitroreductase
MSTPVIDRTAPTEHPVLDVLAGRWSPRAFDAETPIDEAKLAAALEAARWTPSANNTQPWRFIVARRGTALHAQIVESLMGFNQQWAGNAAALVVAVAETATEDGTPLTHAVYDLGQAVAHFSVQAHNDGLYVHQMSGFDPEVVREFADLDPRFSAVTVIAVGDFGDVEALPDVLKEREVAPRVRRPISETVILSA
>NZ_CP013859.1|WP_067195651.1|581657_582602_+|LysR-family-transcriptional-regulator
MLDVNRLRMLVELSRRGTLSAVADALSYSKATVSQQLAALEREVGVPLLRRVGRGVQLTPQGDVLVAEAVGVLDRLEHARVAVAESLAEVTGTVRVAVFQTAAHALLPPALLALQAQHPSLRVDVTECDPETGLVGVAGRDFDLMLAEQYPGHSRPITPDLDRVMLAHDAIALALPPGVPREVDPLAALRSTSDEPWVLEPQGTASRAWAEQLCRSAGFEPDVHFEVADLTTHIRLIRAGLAVGLLPGLVWAGDAPTLDLVPLPGAPRREIFSAARRVSAASPAIRAVRRALADAASPAGSVPAGSLGKPPEVP
>NZ_CP013859.1|WP_067195648.1|577990_581524_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase
MTVVDAASDAARRPRTDEVAALVQRWLAESETHPVEPAAQRLSEVLKDPNGLAFTVGFVDGVMRPEDLKVAARKLADLSDITPALLPGYLRLAIKAGGFWAPVLPGVVVPIARRVLRAMVGHLVLDATPSKLGPAIAKLRKSGNRLNLNLLGEAVLGEREAGRRLKGTYDFLARDDVDYVSIKVSSVVSQLSMWSFDEAVADVVEKLTPLYELAAAAEAKGKAKFINLDMEEYRDLDLTIAAFTSILDQPALKDLEAGIVLQAYLPDALGAMQRLQEWAAARRAKGGAPIKVRVVKGANLAMEEVDAKIHGWPLATYGTKQDSDTNYKRVLDWAMTPERLHAVRIGVAGHNLFDIAYTWLLAKARGVTDAVEFEMLLGMATGQAEAVRKDVGNLLLYTPVVNPAEFDVAIAYLVRRLEENASPENFMSAVFELSSNPELLQRERQRFERSLAALEAEVVAPAPNRTQDRSTLRLAADAKEQGNAKRTLNEERGHETTDAMTGFANEPDTDPALAANRAWGRDILRRSTSSTLGQGAIAAARIETAEQLDAVFSAASAAAEKWAALPASDRAAVLHRAGRELAARRGELIEIMAHEAGKTIAEADPEVSEAIDFAHYYAERALDLERIEGAEFVPSRITVVTPPWNFPVAIPAGGVLAALASGSSAVIKPAKLTQRCGAVMVEALWAAGVPRDLLALVDLGSRELGTRLVSSPEVDRVILTGAYETAKLFRSFRSDLPLLGETSGKNAIIVTPSADLDLAAADVARSAFGHAGQKCSAASLAILVGSVADSKRFERQLVDAVRSMRVGLPDDPATQMGPIIEPANGKLLKALTTLDRGERWLVEPRKLDAEGKQWTPGVKIGVAPGSTTHLTEFFGPVLGIMRAKDLDEAIRLQNAVDYGLTAGLHSLNSEEVATWLERVEAGNLYVNRGITGAIVQRQPFGGWKRSAVGAGAKAGGPNYLFGLGEWKPAELPATASDAAVTSDVAALLAAASDLDATEREWLQRAAASDERAWTTEFGIVTDKSGLGVERNLFRYRPVAVDVRIAEDAPLVDGIRVIAAALRSGSPFTVSAPALPAKVEKALRSRGVTVEHEKDAAWVRRFAKSVAKGENSWQRVRLVGGEASTLFAAIDGLPDVAVWSHAVTGAGRVELLPFLHEQAVSITNHRFGNPTALSDGVI
>NZ_CP013859.1|WP_157540844.1|598196_598373_+|hypothetical-protein
MILIIALLVLAGWAIVATIIEVRRDGYRAVPTDWTRVAPAERHGREALDSAEIGRIHR
>NZ_CP013859.1|WP_067195690.1|599105_599570_+|hypothetical-protein
MSEPHFPPAQPSGTPGQGTPGYPQPSGAPGQDAPGYPQPSGTSPYGSPAPAPQPGNPLGRVAFLIAVIAFALGALVNLITPFLFASGNYDVADSLSTVVNILVLLGEVAALVLGLIALRRPEPRLLAAIAVGIAGAGVVIRLLGWASTLLWYVF
>NZ_CP013859.1|WP_067202035.1|599680_600907_-|glycosyltransferase
MHVVFFGDQHLDSLGGAQVSMRLQRAFLERAGHTVTVVAPRMHGPRAATVPDPANVDLPSVPLTVDREYSMSWPGRATDRHLDEAMTRRLPVDLVHVQADFWGAFIGHRFAARHGIPVVHTMHNRVDVGIAAVTPLHRPALAFLNAWRRRALRGIGEPVAGRDGWSYLRGLAAGASAVTAPSTHFARRLEQNDVFRPVDVVWNGIDDDLRDATLAAAPEERMPGRPRFVWLGRMSPEKRLLPFLEAFVAAGMDAELEIIGGGAQRAAAERIVTGMPHVRFAGRLDYAETLARIAAADALVQTSIGFETQGMTPFEAATLGTPSVISDPDIAAELGGGLWAVPDPSEPGQSAREREARRIAALAETLRTAASDIASGRAPVPLPSVAEAFRQSSRTAAMIEIYERVLAG
>NZ_CP013859.1|WP_067195693.1|600909_602178_-|glycosyltransferase
MYLKAASVTSTDDPTEPSRTPDADSAAAEPATGQRPLRILLGCDTFSPDINGAARFAERLAAGLVQRGHDVHVTAPNTAYRRTAPRTEVIEGEPMTLHRLPSVRWAPHDWLRFVWPWRSKHYARKVLDAVQPDVVHIQSHIVIGRGLARIARQRGIPVIATNHVMAENILDHTTMPKFIDDLVLKFAWADARRTFALTRAITTPTRRAADFLERTVDVSGVIPVSCGIDRSQYTPVIGPREKNRIVFVGRLTAEKQVEVILKAMTKLDPGLDASFDIVGGGDQRKQLEHLAAQLGLADRVTFHGRTTDEELRALLSRASVFAIASIAELQSIATMEAMASALPIVAADAVALPHLVHDGENGYLFEPGNADELAARLTDVLTAEPAEYERMQRASLDGVVIHDINRTLDTFEALYRDEPLPE
>NZ_CP013859.1|WP_067195696.1|602310_602901_+|hypothetical-protein
MRLAADADPRLWIPVTDSFGFRGRRHRKAAIRMLLSQATSALGATPRPGSRFGAWAMSQAAPLLMKRADGRVLVWTWKADPELVVAMVTAQALTPEVRIARASMPMDYDDTESFSSRWLGAGEKLVVPIPESPTAPPFATYTWDTGTHLVTLTAICSDRERFGTVIGALDDLARSIRVADEITGGESPEVLRLPPA
>NZ_CP013859.1|WP_067195699.1|602946_603486_+|VOC-family-protein
MNDFFPAFEMGPTSERGARAVAPEIFRGIYAMPAFVTIPTDDLDASVDFWLRGLGFIELFRMPGVVHLRRWAFQDVLLVPGEPDGPEHPPAMSVSFSYVLSELDGVAEACAELRPGSTTGPRDTPWLTRDVEVITPEGARVICTAPREFDPSSAEAQSLAAAGIPVPGTDEEGDNGHRG
>NZ_CP013859.1|WP_067195703.1|603469_604282_+|MerR-family-transcriptional-regulator
MVIVADREVRTGVTVGRAAELTGVTVRTLHHWDEIGLARPSLRSPAGYRSYTDDDLHRVQRIVAYRAAGLGLEAIREVVDDTTAEIGETLRAQRAQLAERMRELERLDQRLERLMQAHERGILLDEAEQAELFGPDWDPSQTSQARIAWGGSLQWAQFAERSATRGREEWRALHDAMSAVQSGLADALSRGVAAGSDEANELVERHREVFSHFFPLSREMQVCLGRMFEADAGFAAYYDGIRPGLASWFRQIIDASARAHGIDPDAAVWR
>NZ_CP013859.1|WP_067195706.1|604597_607591_-|alpha-mannosidase
MHDDTSLTVGRVTRVLDERIRPAIHSASVPLTVEAVQLPGEPIPPAEGLALDFAPVAVPAPWGPAWSTTWFRLTGRVPAGWAGRRVEAVIDLGFDINMPGFQCEALVYRPDGSPVKSINPRNQWLPIADTAEGDEPVELYLEAAANPVLLDYHPFLPTQEGDILTSSPEPLYRTRRIDLAIFEPEVFELSLDLEVLSELQAELPATSPRRMRILQALDDALDVLDLQRIAETAADARAQLADVLAAPAEASAHRISAIGHAHIDSAWLWPVRETIRKVARTTSSMTALLDEHPEFQYGMSSAQQYAWLKEHRPEVYERVKAAVAEGRFLPLGGMWVESDTVMPSGESMVRQFSYGQRFFEREFGIRSKGVWLPDSFGYSPALPQLMRRAGFEWFFTQKISWNQQNVFPHHTFLWEGIDGSRVFTHFPSMDTYNSQLSGAEVAKAARQFKENRLTSRSIAPVGWGDGGGGTTREMTGKAARLRDLEGSARVEWEHPDVFFEAAKAELPHPAVWVGELYLELHRGTLTSQHATKALHRWAEHALVEAELWAATDAVRTGAAHPRAEFDRLWQTLLLHEFHDILPGTSIAWVHREAVEVLSGVLDDARALSDAARRSLAGDGDRALVFDPLAGDAVETRSPDGDGGSETAAVSLTEESGGYRLENELVSVLISADGLITSAVDKATGREAVAAGRAANLFQLHQDFPNMWDAWDIDRYYRNSVTDLTDAAEVTASVEAGTAVVRVVRRFSESTIEQTIVLRPGSRTVLLRNDVDWHETEKLLKLAFPLDVQATHTEAETQFGYQSRVTHTNTSWEAAKFETSMHRFVLVREQDFGVALVNDSIYGYDTTRDADDDGVTTTVRLSLLRAPRFPDPDTDHGHHEIEVGFVIGADAAIATAEGRRLNAPATVVRGGREVEPLVSVDGEGIVVSAVKLADDDSGDVIVRVYEALGRRAAGVLEIGFEHREVREVSLIEDELESPRRGGELQLRPFEVRTLRIAR
>NZ_CP013859.1|WP_067202039.1|607716_608544_-|carbohydrate-ABC-transporter-permease
MKPSLGGLIGRYALLLIVLAIMVFPFLWQMSTSFKGATENIYDFPPQLIPQAPTLDNYAEVFRTIPVLDYAWHSLLVGVGTVVTNVVFATIGGYALGTMKFRGKWVVLAIIFSTLLLPGEVTLTSQYLTVKSLGLANTLWGVFLPGAIAAINVLLMMAACRMIPPDTLDAATIDGANTMQRLRHIVWPNVRGMVSVVALFAFIGAWDDFLWPLVVLSDPANYTLTVGMQYLSSNFSANPRVIAAGTMIALVPIIVLFAALQRQFFKGVEEGSVKG
>NZ_CP013859.1|WP_067195708.1|608681_609629_-|sugar-ABC-transporter-permease
MKRQSWYTPYLLVLPAVVWVFVFALWPFLNTVVLAFTDARPLRPAEFVGLANFAKLFEDERFGYALTTSLVYVVVCVPLLTFLPLLLALLVHTKIPAIGFFRTTFYFPVIASAVVVAIVWEFLFSGSGTINSALKFFGVVDRPIEFLSDRWLLIGCAIGLTVWKGLGYYMVVYLAALGNVGRELHEAAAMDGAGRLRRFWSVTVPGVRGPMMLVSVLVCVGAMRVFTELYVLSNGSGGPGGRAMSMVMLIQSMGKGLNGQVGYASAISLVLFLLTLVPLAVVGVINNSDTLKDALAARRTARAARLARRAQGATR

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_CP013859_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_2

636528-636606

Orphan

Consensus_repeat	Method
CACAGCGCACATCACCGTAGGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013859_2

>merge|NZ_CP013859|2|636528-636606|CRISPRCasFinder
CACAGCGCACATCACCGTAGGAGTGCACCCGGCGCACACGCGAAACACACCGGTCACACAGCGCACATCACCGTAGGAG

>NZ_CP013859|2|2|636528-636606|CRISPRCasFinder
CACAGCGCACATCACCGTAGGAG	TGCACCCGGCGCACACGCGAAACACACCGGTCA
CACAGCGCACATCACCGTAGGAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067195750.1\|635119_636436_-\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|367155
NZ_CP013859.1\|WP_083511072.1\|634367_634838_-\|glyoxalase	unknown	unknown	gnl\|CDD\|319906
NZ_CP013859.1\|WP_083511075.1\|639053_639893_+\|uroporphyrinogen-III-C-methyltransferase	unknown	unknown	gnl\|CDD\|381169
NZ_CP013859.1\|WP_067195740.1\|628717_630094_-\|NAD(P)-binding-protein	unknown	unknown	gnl\|CDD\|366721
NZ_CP013859.1\|WP_067195760.1\|641760_642687_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223566
NZ_CP013859.1\|WP_067195744.1\|630690_631671_-\|DnaJ-domain-containing-protein	unknown	unknown	gnl\|CDD\|237665
NZ_CP013859.1\|WP_067195738.1\|627989_628634_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_083511073.1\|636661_637531_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239509
NZ_CP013859.1\|WP_067195770.1\|647268_647832_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|173776
NZ_CP013859.1\|WP_067195767.1\|645833_647051_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|225371
NZ_CP013859.1\|WP_067195757.1\|639939_641340_+\|pyridine-nucleotide-disulfide-oxidoreductase	unknown	unknown	gnl\|CDD\|215457
NZ_CP013859.1\|WP_067195742.1\|630222_630645_-\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133394
NZ_CP013859.1\|WP_067195737.1\|626404_627697_-\|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP013859.1\|WP_067195748.1\|632337_634197_-\|molecular-chaperone-DnaK	unknown	unknown	gnl\|CDD\|234715
NZ_CP013859.1\|WP_067195765.1\|643596_644058_-\|DUF3817-domain-containing-protein	unknown	unknown	gnl\|CDD\|378962
NZ_CP013859.1\|WP_157540850.1\|642749_643436_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_083511074.1\|637986_639057_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223673
NZ_CP013859.1\|WP_083511076.1\|644158_645076_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP013859.1\|WP_067195734.1\|625367_626333_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP013859.1\|WP_067195746.1\|631678_632335_-\|nucleotide-exchange-factor-GrpE	unknown	unknown	gnl\|CDD\|271355

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_067195750.1\|635119_636436_-\|HNH-endonuclease	gnl\|CDD\|367155	pfam02720, DUF222, Domain of unknown function (DUF222). This family is often found associated to the N-terminus of the HNH endonuclease domain pfam01844. The function of this domain is uncertain. This family has been called the 13E12 repeat family.	2.02178e-11
NZ_CP013859.1\|WP_083511072.1\|634367_634838_-\|glyoxalase	gnl\|CDD\|319906	cd07242, VOC_BsYqjT, vicinal oxygen chelate (VOC) family protein similar to Bacillus subtilis YqjT. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	9.49345e-27
NZ_CP013859.1\|WP_083511075.1\|639053_639893_+\|uroporphyrinogen-III-C-methyltransferase	gnl\|CDD\|381169	cd11642, SUMT, Uroporphyrin-III C-methyltransferase (also known as S-Adenosyl-L-methionine:uroporphyrinogen III methyltransferase, SUMT). SUMT is an enzyme of the cobalamin and siroheme biosynthetic pathway. It catalyzes the first of three steps leading to the formation of siroheme from uroporphyrinogen III; it transfers two methyl groups from S-adenosyl-L-methionine to the C-2 and C-7 atoms of uroporphyrinogen III to yield precorrin-2 via the intermediate formation of precorrin-1. Precorrin-2 is also a precursor for the biosynthesis of vitamin B12, coenzyme F430, siroheme and heme d1. This family includes proteins in which the SUMT domain is fused to other functional domains, such as to a uroporphyrinogen-III synthase domain to form bifunctional uroporphyrinogen-III methylase/uroporphyrinogen-III synthase, or to a dual function dehydrogenase-chelatase domain, as in the case of the multifunctional S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase/dehydrogenase/ferrochelatase CysG, which catalyzes all three steps that transform uroporphyrinogen III into siroheme.	7.89749e-93
NZ_CP013859.1\|WP_067195740.1\|628717_630094_-\|NAD(P)-binding-protein	gnl\|CDD\|366721	pfam01593, Amino_oxidase, Flavin containing amine oxidoreductase. This family consists of various amine oxidases, including maze polyamine oxidase (PAO) and various flavin containing monoamine oxidases (MAO). The aligned region includes the flavin binding site of these enzymes. The family also contains phytoene dehydrogenases and related enzymes. In vertebrates MAO plays an important role regulating the intracellular levels of amines via there oxidation; these include various neurotransmitters, neurotoxins and trace amines. In lower eukaryotes such as aspergillus and in bacteria the main role of amine oxidases is to provide a source of ammonium. PAOs in plants, bacteria and protozoa oxidase spermidine and spermine to an aminobutyral, diaminopropane and hydrogen peroxide and are involved in the catabolism of polyamines. Other members of this family include tryptophan 2-monooxygenase, putrescine oxidase, corticosteroid binding proteins and antibacterial glycoproteins.	4.73756e-26
NZ_CP013859.1\|WP_067195760.1\|641760_642687_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	1.48659e-43
NZ_CP013859.1\|WP_067195744.1\|630690_631671_-\|DnaJ-domain-containing-protein	gnl\|CDD\|237665	PRK14295, PRK14295, molecular chaperone DnaJ.	3.80755e-86
NZ_CP013859.1\|WP_083511073.1\|636661_637531_+\|hypothetical-protein	gnl\|CDD\|239509	cd03416, CbiX_SirB_N, Sirohydrochlorin cobalt chelatase (CbiX) and sirohydrochlorin iron chelatase (SirB), N-terminal domain. SirB catalyzes the ferro-chelation of sirohydrochlorin to siroheme, the prosthetic group of sulfite and nitrite reductases. CbiX is a cobaltochelatase, responsible for the chelation of Co2+ into sirohydrochlorin, an important step in the vitamin B12 biosynthetic pathway. CbiX often contains a C-terminal histidine-rich region that may be important for metal delivery and/or storage, and may also contain an iron-sulfur center. Both are found in a wide range of bacteria. This subgroup also contains single domain proteins from archaea and bacteria which may represent the ancestral form of class II chelatases before domain duplication occurred.	2.72707e-14
NZ_CP013859.1\|WP_067195767.1\|645833_647051_-\|MFS-transporter	gnl\|CDD\|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	3.01536e-59
NZ_CP013859.1\|WP_067195757.1\|639939_641340_+\|pyridine-nucleotide-disulfide-oxidoreductase	gnl\|CDD\|215457	PLN02852, PLN02852, ferredoxin-NADP+ reductase.	2.88493e-117
NZ_CP013859.1\|WP_067195742.1\|630222_630645_-\|MerR-family-transcriptional-regulator	gnl\|CDD\|133394	cd04766, HTH_HspR, Helix-Turn-Helix DNA binding domain of the HspR transcription regulator. Helix-turn-helix (HTH) transcription regulator HspR, N-terminal domain. Heat shock protein regulators (HspR) have been shown to regulate expression of specific regulons in response to high temperature or high osmolarity in Streptomyces and Helicobacter, respectively. These proteins share the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their conserved N-terminal domains contain predicted winged HTH motifs that mediate DNA binding, while the dissimilar C-terminal domains bind specific coactivator molecules.	1.36419e-29
NZ_CP013859.1\|WP_067195737.1\|626404_627697_-\|sugar-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.27695e-51
NZ_CP013859.1\|WP_067195748.1\|632337_634197_-\|molecular-chaperone-DnaK	gnl\|CDD\|234715	PRK00290, dnaK, molecular chaperone DnaK; Provisional.	0
NZ_CP013859.1\|WP_067195765.1\|643596_644058_-\|DUF3817-domain-containing-protein	gnl\|CDD\|378962	pfam12823, DUF3817, Domain of unknown function (DUF3817). This domain is of unknown function. It is sometimes found adjacent to pfam07690 and pfam03176 which are both transporter domains.	1.44914e-16
NZ_CP013859.1\|WP_067195770.1\|647268_647832_-\|hypothetical-protein	gnl\|CDD\|173776	cd01026, TOPRIM_OLD, TOPRIM_OLD: topoisomerase-primase (TOPRIM) nucleotidyl transferase/hydrolase domain of the type found in bacterial and archaeal nucleases of the OLD (overcome lysogenization defect) family. The bacteriophage P2 OLD protein, which has DNase as well as RNase activity, consists of an N-terminal ABC-type ATPase domain and a C-terminal Toprim domain; the nuclease activity of OLD is stimulated by ATP, though the ATPase activity is not DNA-dependent. Functional details on OLD are scant and further experimentation is required to define the relationship between the ATPase and Toprim nuclease domains. The TOPRIM domain has two conserved motifs, one of which centers at a conserved glutamate and the other one at two conserved aspartates (DxD). The conserved glutamate may act as a general acid in strand cleavage by nucleases. The DXD motif may co-ordinate Mg2+, a cofactor required for full catalytic function.	0.00928097
NZ_CP013859.1\|WP_083511074.1\|637986_639057_+\|ABC-transporter-permease	gnl\|CDD\|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	1.12931e-54
NZ_CP013859.1\|WP_083511076.1\|644158_645076_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.07736e-27
NZ_CP013859.1\|WP_067195734.1\|625367_626333_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.54975e-82
NZ_CP013859.1\|WP_067195746.1\|631678_632335_-\|nucleotide-exchange-factor-GrpE	gnl\|CDD\|271355	cd00446, GrpE, nucleotide exchange factor GrpE. GrpE is the adenine nucleotide exchange factor of DnaK (Hsp70)-type ATPases. In bacteria, the DnaK-DnaJ-GrpE (KJE) chaperone system functions at the fulcrum of protein homeostasis. GrpE participates actively in response to heat shock by preventing aggregation of stress-denatured proteins; unfolded proteins initially bind to DnaJ, the J-domain ATPase-activating protein (Hsp40 family), whereupon DnaK hydrolyzes its bound ATP, resulting in a stable complex. The GrpE dimer binds to the ATPase domain of Hsp70 catalyzing the dissociation of ADP, which enables rebinding of ATP, one step in the Hsp70 reaction cycle in protein folding. In eukaryotes, only the mitochondrial Hsp70, not the cytosolic form, is GrpE dependent. Over-expression of Hsp70 molecular chaperones is important in suppressing toxicity of aberrantly folded proteins that occur in Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis, as well as several polyQ-diseases such as Huntington's disease and ataxias.	8.27495e-39

>NZ_CP013859.1|WP_067195750.1|635119_636436_-|HNH-endonuclease
MTALADATIEQMGALRGLTEALVEVDRALSGVLAVKEGLLAVGARLAADMAGDGDPGAELSLRSVAAEFATALRVSDRTVQARMAEAEMKVSLFPEVWKAQGAGRISSGHARVILDAGMYLDDEASRHAYAEQMIAFAETESPNRVGRLARRVAERFQARTADERHRVARRERRVWVTEAADGMAQLGLLGPAALVQGAFSRLTAMAERVQNGLSPDGSDSADAATDPVDSAASSPDDRRIDEIRCDLALDLMLSGAPAGHDTREGVLAAIAGHVSVTVPVLTLMGVDDAAAEIDGRMPVDTATARRLAGASAGWERILTHPVTGGVLAVDRYRPSADMIRYLKSRDVRCRFPGCGRAAADCDVDHTADAALGGATSRENLGDLCRRHHVLKHHSPWQVEQLGGGVFAWTSPTGKTYIDHPPPQNTVTFTDADGPPPF
>NZ_CP013859.1|WP_083511072.1|634367_634838_-|glyoxalase
MAGIHHVELWVADLAEARAEWGWLLQAVGFARTSEWPGGESWEVGGAYLTLTTAPALSGPVHDRRAPGVNHLAFRAGPPDRVDTIMAEAQQHGWRPLYHDRYPHAGGPGHYAGWLENSAGFKAEIVADPEIVADPEIVADPEIVADPEIVAAEPAG
>NZ_CP013859.1|WP_067195748.1|632337_634197_-|molecular-chaperone-DnaK
MARAVGIDLGTTNSVVSVLEGGEPKVIANAEGFRTTPSVVAFTKDGEVLVGETAKRQAVTNVDRTISSVKRHMGTDWTFDVDGKKWTPQEISARILMKLKRDAEAYLGDTVTDAVITVPAYFNDAERQATKEAGEISGLNVLRIINEPTAAALAYGLDKGKEDELILVFDLGGGTFDVSLLEVGKDDDFSTIQVRATAGDNRLGGDDWDQRLVDYLIKQFKETTGVDVSADKIALQRLKEAAEQAKKELSSSTSTSINLPYLSLTESGPVSLSETITRAKFEDLTKDLLDRTKKPFEDVIREAGIKVSDISHVVLVGGSTRMPAVAELVKRETGKEANKGVNPDEVVAVGAALQAGVLKGERKDVLLIDVTPLSLGIETKGGMMTKLIERNTAIPTKRSETFTTADDNQPSVAIQVFQGEREFTRDNKPLGTFELTGIAPAPRGIPQIEVTFDIDANGIVHVSAKDKGTGKEQSMTITGGSSLSKEDIDRMVREAEEHAAEDKKRREAAEVRNQAEALAYSIEKLIADNDDKLPEDVKTDVKADVDALKSALAGDDDDAVKTAFDKLNQSQTKLGEAIYAQSQADAAAGAPSGDAPAGDASSDEDVIDAEVVDDEDEKK
>NZ_CP013859.1|WP_067195746.1|631678_632335_-|nucleotide-exchange-factor-GrpE
MTDKNFDSNDSVPEPVEGREGSDAQASGPAPQNPDFDAPQNPDSDEARAAEHSDDDLTVDDILNADQTDEAAAAETAAIADAEHLVNDLKRLQAEYANYRRRTEEQRQVEIERAKGEAAKGLIPVLDDLDRAGQHGDLVEGTPFAVIADKIRAVVERLGVVAYGEAGEEFDPQRHEAIFQQPTPGAEKTTILEVVEVGYRLGEVELRPAKVVVAVPAE
>NZ_CP013859.1|WP_067195744.1|630690_631671_-|DnaJ-domain-containing-protein
MASQDWFDKDFYKILGVSKDVSDADLKKTYRKLARKYHPDSNPGDAAAEAKFKEISEAYSVLSDAEQRKEYDEIRAMGSGARFTASGSGAGGFEDVFSRFGQSGRGQTADFEDIFAMFNQGGGGFGSGRFGQTSGGFRGFGGPSRGADVTARTTIDFTTAVQGETITLQGDDGKPFKVKIPAGVSDGQKIKLRGRGRPSPDGGENGDIVVQITVRPHPVFTREGLNLRVVVPVTFTEAALGATIEVPTLGGDPVKLRVAPGTPSGRVLRVKGRGVTTTKGTGDLLAELQVAVPSHLDEAAREALERFQELEPDENPRADLLAKARR
>NZ_CP013859.1|WP_067195742.1|630222_630645_-|MerR-family-transcriptional-regulator
MADKRMDADTPVFAIAVAAELSGLHPQTLRQYDRIGLVVPGRTSGGSRRYSTRNIEQLREVAQLSAEGMSLPAIARLLDLEDENRMLRRRITELEGALRAERENRPGARVFAAGSGGVVPMPGGRRIRRSTEVVLWRPRG
>NZ_CP013859.1|WP_067195740.1|628717_630094_-|NAD(P)-binding-protein
MRITRRTLLIGAGAGVVGVLLASCTPEPVPTPTPTPDRSPSPKPTPMTGPTPSAFARSTWTTDAFSLGAVSFTPAGTAAIARDALAAPVDDRLFFAGEATDADAPGTMGGAFRSGIRAAEEIIATAGYGERVAIVGAGLAGAAAASRLAGTGFALTVFEARDRTGGRVHAIVDEATWPVPAQLGSWTLSAADSDVAAEVDDLDIRTAQLTTPLWRSADGDVTAPSPQAVLDAITAAQALPADVSLADALTQAGADLDDPALAALLSSLTATAGADAADLSSWFPPAVPGDDRLAVLGDLGAVFDRLLDGVKVSLSSPVSRVAYDDAGVSLGIATGESLSFDRVLLTVPLGVLQAGGVDFAPKLPFGQRGAIADLGNGFIETVWLRFDEPLIETDAALWHVVGGDAVIRTWVNLAPATGEPLLVGVVGGAAAEDFAGLDDDAALAAALNSLAPFLDQQS
>NZ_CP013859.1|WP_067195738.1|627989_628634_+|hypothetical-protein
MKARTIFGVLRLAAAIVCLVALVHRLFWGLSSQTIAGDNFFAYLTVQSNCALVVVLVIGAVLAFARAADPRWFTVALSLVLTWTITAGLAFALIVWQAGIRGIRVDVPWSDQVLHFWLPACTAIAWVLTPGHRGVPWWIVPVSLAFPLAWGGVTMWRGPIVGWYPYYFLDPRQVSGPVEFLATSGVALAIFALVASALVLISRMRRPGHERPEV
>NZ_CP013859.1|WP_067195737.1|626404_627697_-|sugar-ABC-transporter-substrate-binding-protein
MKLNLADRTRRARALRMTGVAAVAAVALAGCASGTDQTGSDSAGGELTFSNWQFLEDGKGPILWDAVKGYTGPNDDIELTKVEIPFANYADKLSTELGAGGGPDVMVLQDSQFASLVDAGVLEPLDDIADELGDSLNNTNEAGVVDDTQYGFNWERPTYSTVIYNKDIFAQLGLEVPTTFDEFLTTAKAIKDQLGIAGWAGRHQTAEIDGWTLEMANWIYGFGGELSDGKKLTIDKAENVEAVEAFLETFASGVAPIGDDASTFRAKFGQGQVGMLFENSGVATTITSNPDNVVNGQNLGAAPLPLAHPGSNSQLIIAVNANSDNKEAAKDFVRWVLSDEGQTAIRAGLGASAMATDVEPDPAFLEANPWATQFLEAAKTSKSTLVEGFETESKVIWREVLTAVEDLRVNGGDVKTKLAEVQKSLEAELG
>NZ_CP013859.1|WP_067195734.1|625367_626333_-|sugar-ABC-transporter-permease
MATPTLEAPPAARAAAPRRRPRSGSAVGRFVERNGAYLFLFPAIAYLAIFTVFPLIRGVLLSFTATKLVNPAGGRGVGLENYDYLLSSDRFWTSVVTTLLYTLFTVVFAVGIGTAGALLLNTAFKGRSIVRAIATIPWAVPTVAAALIFVWIYNNEQGILNRTTAALGLGQHGWLVDPQYGLFAVTFATVWKLTPLVMLVMLSALQSVPHELREATWVDGATRFQSFLAVTLPHIMPTVRVITLLMTIWSIRRFEIIFLITGGGPLDVTNTLVVNVYRTAFQDQNLGRAAAIGALGLVLSLLVTVVYFVVEQIQERQENQR
>NZ_CP013859.1|WP_083511073.1|636661_637531_+|hypothetical-protein
MSRPLLLAVSHGTADAAGSRAIAALVDSARQSLPDVDVRAAFVDVQEPDAAELAPRLGGRVVIVPLLLSSGFHVHHDLHGIAARRPRTVVADPLGPDPRLAEVLASRLDALHEHAPEHDERKHEGHEHEPEHEPEREPGGDHKRHEPEPEPEPEHDERDHKRHEPEPEPERDRQEQKRHAPVILAVAGSRDERSLTDAEAMASLLAARTGRDIHLAYLAARRPSLPTALAEHPDAVVSTFLLARGYFFDLASRQAAGRMLTAPLLDGGEVPPALTDLVISRYLDAAARL
>NZ_CP013859.1|WP_083511074.1|637986_639057_+|ABC-transporter-permease
MPAETPETLTHTHGTHETRTHGTHETYTHGTHGAAGTALTGASGTTLTTGAGTTLTTGAGTAPTTAAGTADDLRTLSAGLDRLQSDAEPTRSRWREALAKALPPVVLLLALLALWQLYVVIAHPRPDKAPSPAGVLGALGEAWSTGRLQEAVATSLERGIIGFLIAIAVGTPLGLLLAEWRLLRRAAGPLISGLTVLPSVAWVPAAIIWFQLSDATVYFVILMGTIPSIVNGLLGGIDQVPPQLRRVGVVLGASRWQLATSVVLPAALPGYLAGLKQGWAFSWRSLMAAEIIAVGGSIGFGLGAMLGQARELADLAGVLATILLILAIGIVIELVLFGPLERRMLRDRGLLLGGAK
>NZ_CP013859.1|WP_083511075.1|639053_639893_+|uroporphyrinogen-III-C-methyltransferase
MTGRVTLVGAGPGDAGLLTLRGLRALQEADVIVADRLGARPVLEQLAADGIRLTAEIVDVGKLPGHHPVPQDGINDLLVQRALAGDRVVRLKGGDPFVFGRGREEQQHCEAAGVPVDVVPGVTSAVSVPAVAGIPLTHRGVATSFTVVSAHDQIDAIPGGGEHTVVLLMGVNTLAHSAHVLASGARGPECPVAIVEDGYGPRERVTIGTLGSIAHDAAARQVRSPAVIVVGYVVRLSPHAPETREPVGNPRDKPHWIDALLGGLAVDAGLASAVERTLG
>NZ_CP013859.1|WP_067195757.1|639939_641340_+|pyridine-nucleotide-disulfide-oxidoreductase
MTRSPLSLRVAIVGAGPAGIYAGNLLADAVRDRSGTVEIDLFESLPAPYGLIRYGVAPDHTRIKGIVGSLHEMLDAFPETADGGPAPARRTIRFLGNVEIGRDLSLSELRSRYHAVILATGAIRDAELPIPGVDLPGSFGAADFVAWFDGHPDVARTWPLDAASVAVIGNGNVALDVARILAKHPVDLRTTEVPDTVLSGLEASAVTDVHVFGRRGPADIKFTPIELRELGEVRDVDIVLHDEDFDGVDPASAPTNQLKVMLRTLNAWRDRPAGTASRRLHLHFWHSPVEILGDERVEGVRFERTRAGADGTVVGTGEFRDHAVQAVYRAVGYYGTRVVGAPFDEARGVIPNEGGRVTDEPGLYATGWIKRGPVGLIGHTKSDALETITNLVADAEAGRLAAPEVDGDIVDLLEADGAEYTTWDGWLALDAHERRLGETHEYVRERVKVVPREEQVAVSRDGTLVR
>NZ_CP013859.1|WP_067195760.1|641760_642687_+|NAD(P)/FAD-dependent-oxidoreductase
MTGTAPYDVLIVGGGPAGLSAALNLGRSLVRVLVVDADRPRNAATLSSHGFLTRDGVPPHELRKLARAELESYPTVEVRSRVRVVELRRDGDTWTAGIGRTEASETVSAGVVLLATGLRETLPDVPNLRGFYGMSLFSCAACDAWELRGRRLALIGESADLAVRARLLSRWTQNLTLFTHGSRAVTAEEEAELAAAGVAVLRHPIVELLGAKGRLEGIRLADGSIVEADGGFVRPHWENDLSFLDGVAPAVDENGHLITDRSGRTDVPGLYAAGDAAAGPQQLIVAAGAGARVAAVIVHDAVGVTTAH
>NZ_CP013859.1|WP_157540850.1|642749_643436_+|hypothetical-protein
MTRTSGGRAAAAATIVGLALLPLSGCLYAQIPEHPTAVESTPASDGPADEPADEPSDPPADAPADGLSFADGASIPASAHIEWGDGFFMDDGWTVTSPDDGNGGWAYGTTDGTCVARFWQGDVSGLPLVAGDDSASSDALLAYVIGDASAADITPLAVTASLGYGTGSNQTLEARQIIGEDGDRRWAITARAFTANAHGVYVIADCTGGDLEAVFAEIVEKNPVVVSG
>NZ_CP013859.1|WP_067195765.1|643596_644058_-|DUF3817-domain-containing-protein
MFTLPSRLFRVLAIAEAVTWTILIAALVSRALGAPGIVVTIGGGIHGFVFLAYGATAILVALNNRWHAGVAVLAVASAIVPYATVPLEIWLHRTGRLAGEWRLEESADPRDRRWYDRTMRWFLRRPWVLGGLIAAAVVALYVVLLLVGPPGGR
>NZ_CP013859.1|WP_083511076.1|644158_645076_+|helix-turn-helix-transcriptional-regulator
MVTVDPEALSQVLGAVDLRVGIARRRRLDAAALLPLSTGDSTLVYVARGQVHGIPPLDSGCRLTVERSSQQVAVDQGRPASSLRAGDAFLTLGRASLALEADAETELVVVDLALADAASIVDALLPDYITVTGFDRLEPAAAALAAGMGPLDPTACSGRRGDPVICRMMATTVLLSVIRAWAENGCAPEGWPRMSSDPFLDRVVEAIHEQPGRDWTVERLASVGAMSRSAFAERFRSVIGRSPADYVTEVRVDAAKRMLEEGRSVSETSRALGYASDEGFSRAFRRRTGMTPSAWRAAARTPVVA
>NZ_CP013859.1|WP_067195767.1|645833_647051_-|MFS-transporter
MTTTAPVPIAPVSNAPAGRIDRMRYGGLVALMMMGFLLVTAEFLPNGVLTEMADALGVTPGQAGQTVTVTALVGLVVAPTIGLIFPRLDRRSLLVWMALAAAVSNLVVAIAPSLMIVLAARFLLGAAISAFWSMSITVAAALAGPERLGRGVMFTSAGVSLATVAGVPLGVMLSELVDWRMVFALASVLMVLLAVALRAALPSVPAAQAASIRLLVDTVRRPGIGLGLFGHVFVVLGHFLAYTYVRLALERIPDVDASTIVVLLALFGLGGLAGNIAIGLVIDRSFAFLAVIAPLVISAAVLAMILLPGTVAGVAAVVLVWGFFFSSWLIVANTWVGHRMPDRLEAGGSLVVVGFQAAIMIAAGVGGLLVDTLGIELVYVVGAASLLLGAVLFGVSNRARAHGRA
>NZ_CP013859.1|WP_067195770.1|647268_647832_-|hypothetical-protein
MPETTEPRTVVLFEGASDRLAVETAARRLGLSVDELELVDLDGITNLRGRLRMLREAGRRVVGLYDAAEGGYVSSVLRDLGAISHDGSPEDAGFFGCERDLEDEVIAAAGAELVIQTLDARGELARFRVFQGQPAQRERTVEEQLHRFAGTAAGRKARFAADVIAAIPVERMPRPIVALLRAALRGR

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_CP013859_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_3

1092000-1092091

Orphan

Consensus_repeat	Method
CCGAACCGGCCGCTGCTCTGCTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013859_3

>merge|NZ_CP013859|3|1092000-1092091|CRISPRCasFinder
CCGAACCGGCCGCTGCTCTGCTGACCGCCTTCACGTCCGGCCTCGCTGGGGTCGGCGCCGTTCTCCGCGCCGAACTGGCCGCTGCTCTGCTG

>NZ_CP013859|3|3|1092000-1092091|CRISPRCasFinder
CCGAACCGGCCGCTGCTCTGCTG	ACCGCCTTCACGTCCGGCCTCGCTGGGGTCGGCGCCGTTCTCCGCG
CCGAACTGGCCGCTGCTCTGCTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067202205.1\|1100940_1101495_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP013859.1\|WP_067202202.1\|1095599_1097309_-\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224099
NZ_CP013859.1\|WP_067196433.1\|1094487_1095603_-\|LacI-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_CP013859.1\|WP_067202198.1\|1090732_1090999_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP013859.1\|WP_067196418.1\|1088853_1090074_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340883
NZ_CP013859.1\|WP_067196436.1\|1098511_1099594_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270269
NZ_CP013859.1\|WP_067196422.1\|1091060_1091834_+\|type-I-methionyl-aminopeptidase	unknown	unknown	gnl\|CDD\|238519
NZ_CP013859.1\|WP_157540888.1\|1079389_1080280_+\|restriction-endonuclease	unknown	unknown	gnl\|CDD\|225973
NZ_CP013859.1\|WP_083511119.1\|1099931_1100858_-\|NAD(P)H-binding-protein	unknown	unknown	gnl\|CDD\|187542
NZ_CP013859.1\|WP_067196434.1\|1097466_1098480_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226361
NZ_CP013859.1\|WP_067196428.1\|1092775_1093417_+\|NAD(P)H-hydrate-epimerase	unknown	unknown	gnl\|CDD\|223140
NZ_CP013859.1\|WP_067196430.1\|1093546_1094431_-\|3',5'-cyclic-nucleotide-phosphodiesterase	unknown	unknown	gnl\|CDD\|277347
NZ_CP013859.1\|WP_067196411.1\|1083710_1085489_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|197273
NZ_CP013859.1\|WP_067196413.1\|1085481_1086669_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067196438.1\|1101573_1102203_+\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_CP013859.1\|WP_067196426.1\|1092320_1092617_-\|DUF503-family-protein	unknown	unknown	gnl\|CDD\|377364
NZ_CP013859.1\|WP_067196420.1\|1090153_1090459_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223713
NZ_CP013859.1\|WP_067196416.1\|1088072_1088654_-\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|372995
NZ_CP013859.1\|WP_067196415.1\|1086712_1087996_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_157540891.1\|1080280_1083736_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239517

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_067202205.1\|1100940_1101495_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	1.226e-10
NZ_CP013859.1\|WP_067202202.1\|1095599_1097309_-\|iron-ABC-transporter-permease	gnl\|CDD\|224099	COG1178, ThiP, ABC-type Fe3+ transport system, permease component [Inorganic ion transport and metabolism].	8.95689e-64
NZ_CP013859.1\|WP_067196433.1\|1094487_1095603_-\|LacI-family-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	4.30375e-63
NZ_CP013859.1\|WP_067202198.1\|1090732_1090999_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	4.74157e-08
NZ_CP013859.1\|WP_067196418.1\|1088853_1090074_-\|MFS-transporter	gnl\|CDD\|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.05683e-24
NZ_CP013859.1\|WP_067196436.1\|1098511_1099594_-\|extracellular-solute-binding-protein	gnl\|CDD\|270269	cd13551, PBP2_Fbp_like_5, Substrate binding domain of an uncharacterized ferric iron transporter, a member of the type 2 periplasmic binding fold superfamily. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria from the Pasteurellaceae and Neisseriaceae families and is critical for survival of these pathogens within the host. This periplasmic domain (Fbp) has high affinity for ferric iron and serves as the primary receptor for transport. After binding iron with high affinity, Fbp interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ferric iron-binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	4.84172e-114
NZ_CP013859.1\|WP_067196422.1\|1091060_1091834_+\|type-I-methionyl-aminopeptidase	gnl\|CDD\|238519	cd01086, MetAP1, Methionine Aminopeptidase 1. E.C. 3.4.11.18. Also known as methionyl aminopeptidase and Peptidase M. Catalyzes release of N-terminal amino acids, preferentially methionine, from peptides and arylamides.	3.74412e-98
NZ_CP013859.1\|WP_157540888.1\|1079389_1080280_+\|restriction-endonuclease	gnl\|CDD\|225973	COG3440, COG3440, Predicted restriction endonuclease [Defense mechanisms].	4.17732e-12
NZ_CP013859.1\|WP_083511119.1\|1099931_1100858_-\|NAD(P)H-binding-protein	gnl\|CDD\|187542	cd05231, NmrA_TMR_like_1_SDR_a, NmrA (a transcriptional regulator) and triphenylmethane reductase (TMR) like proteins, subgroup 1, atypical (a) SDRs. Atypical SDRs related to NMRa, TMR, and HSCARG (an NADPH sensor). This subgroup resembles the SDRs and has a partially conserved characteristic [ST]GXXGXXG NAD-binding motif, but lacks the conserved active site residues. NmrA is a negative transcriptional regulator of various fungi, involved in the post-translational modulation of the GATA-type transcription factor AreA. NmrA lacks the canonical GXXGXXG NAD-binding motif and has altered residues at the catalytic triad, including a Met instead of the critical Tyr residue. NmrA may bind nucleotides but appears to lack any dehydrogenase activity. HSCARG has been identified as a putative NADP-sensing molecule, and redistributes and restructures in response to NADPH/NADP ratios. Like NmrA, it lacks most of the active site residues of the SDR family, but has an NAD(P)-binding motif similar to the extended SDR family, GXXGXXG. 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. Atypical SDRs are distinct from classical SDRs. 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.	7.689e-59
NZ_CP013859.1\|WP_067196434.1\|1097466_1098480_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	1.03384e-145
NZ_CP013859.1\|WP_067196428.1\|1092775_1093417_+\|NAD(P)H-hydrate-epimerase	gnl\|CDD\|223140	COG0062, COG0062, Uncharacterized conserved protein [Function unknown].	1.40318e-38
NZ_CP013859.1\|WP_067196430.1\|1093546_1094431_-\|3',5'-cyclic-nucleotide-phosphodiesterase	gnl\|CDD\|277347	cd07402, MPP_GpdQ, Enterobacter aerogenes GpdQ and related proteins, metallophosphatase domain. GpdQ (glycerophosphodiesterase Q, also known as Rv0805 in Mycobacterium tuberculosis) is a binuclear metallophosphoesterase from Enterobacter aerogenes that catalyzes the hydrolysis of mono-, di-, and triester substrates, including some organophosphate pesticides and products of the degradation of nerve agents. The GpdQ homolog, Rv0805, has 2',3'-cyclic nucleotide phosphodiesterase activity. GpdQ and Rv0805 belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	2.17546e-61
NZ_CP013859.1\|WP_067196411.1\|1083710_1085489_-\|hypothetical-protein	gnl\|CDD\|197273	cd09176, PLDc_unchar6, Putative catalytic domain of uncharacterized hypothetical proteins with one or two copies of the HKD motif. Putative catalytic domain of uncharacterized hypothetical proteins with similarity to phospholipase D (PLD, EC 3.1.4.4). PLD enzymes hydrolyze phospholipid phosphodiester bonds to yield phosphatidic acid and a free polar head group. They can also catalyze transphosphatidylation of phospholipids to acceptor alcohols. Members of this subfamily contain one or two copies of the HKD motif (H-x-K-x(4)-D, where x represents any amino acid residue) that characterizes the PLD superfamily.	6.48959e-15
NZ_CP013859.1\|WP_067196438.1\|1101573_1102203_+\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	5.31337e-25
NZ_CP013859.1\|WP_067196426.1\|1092320_1092617_-\|DUF503-family-protein	gnl\|CDD\|377364	pfam04456, DUF503, Protein of unknown function (DUF503). Family of hypothetical bacterial proteins.	1.52915e-27
NZ_CP013859.1\|WP_067196420.1\|1090153_1090459_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|223713	COG0640, ArsR, Predicted transcriptional regulators [Transcription].	5.66532e-08
NZ_CP013859.1\|WP_067196416.1\|1088072_1088654_-\|HNH-endonuclease	gnl\|CDD\|372995	pfam14279, HNH_5, HNH endonuclease. This domain is related to other HNH domain families such as pfam01844. Suggesting that these proteins have a nucleic acid cleaving function.	3.0422e-05
NZ_CP013859.1\|WP_157540891.1\|1080280_1083736_-\|NUDIX-domain-containing-protein	gnl\|CDD\|239517	cd03425, MutT_pyrophosphohydrolase, The MutT pyrophosphohydrolase is a prototypical Nudix hydrolase that catalyzes the hydrolysis of nucleoside and deoxynucleoside triphosphates (NTPs and dNTPs) by substitution at a beta-phosphorus to yield a nucleotide monophosphate (NMP) and inorganic pyrophosphate (PPi). This enzyme requires two divalent cations for activity; one coordinates the phosphoryl groups of the NTP/dNTP substrate, and the other coordinates to the enzyme. It also contains the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as metal binding and catalytic site. MutT pyrophosphohydrolase is important in preventing errors in DNA replication by hydrolyzing mutagenic nucleotides such as 8-oxo-dGTP (a product of oxidative damage), which can mispair with template adenine during DNA replication, to guanine nucleotides.	4.3323e-45

>NZ_CP013859.1|WP_067196422.1|1091060_1091834_+|type-I-methionyl-aminopeptidase
MIEILTSDELVRARQAGALVGTILHTLKERTRPGVNLLDLDRWAQELIADAGGQSCYVDYAPSFGRGPFGHYICTAVNDAVLHGMPHDFALADGDLLTLDLAVSLHGIAADAAISFVVGEAASAADLAMIDATERALAAAIAVARPGARTGDLSHAIGSVLRDAGYPINLEFGGHGIGSTMHQDPHISNDGRPGRGYQLRPGLLLALEPWVMADTDDLLTDPDDGWTLRSATGCRTAHSEHTIAITETGAEILTLAR
>NZ_CP013859.1|WP_067202198.1|1090732_1090999_-|helix-turn-helix-transcriptional-regulator
MVRMPLTPADVERGERLGAILRRARGGRSMLSVALDAGISPETLRKIESGRVATPSFSTIAAIAGVLGLSLDEVWAEVGTDAAGRVAS
>NZ_CP013859.1|WP_067196420.1|1090153_1090459_+|helix-turn-helix-transcriptional-regulator
MAGDLPHPERFEIQLTDVLFALSDPERLAIARQLADGPLDMAACHATDPNLPKSTKSHFMKVLREAGVIRNEPNGRRRMLTLRRDDLDARFPGLLDSVLNA
>NZ_CP013859.1|WP_067196418.1|1088853_1090074_-|MFS-transporter
MTTTQPVTVPAAVLDAPRRRSGAAFVLAVVAQITMMVGASAPSPFYPVLAHDIGFGPVVISAVFAVYAVALLLTLLTAGSLSDHIGRRPVAFVGFLLLAGSMVLFWHADSVVVLVLARALQGIASGLLISALSAAVLDLAPAGRERVAALWNALTPGIGLALGALVSAVVLDTTGEPLLDVFAPLTVAYVALAVLFLLAPETAPRRPGALASLSFRLSLPTGIRRDFLHASPAVIAGWATGGLFLSLGANIVRGELGGQAHVWQGLPVTVLAGVGAITALLIRRRSARTSVLFGTAALGVGTLLSLIALGVQSLPFYLVAAAVTGMGFGTAFSGVVASLAPRIPPTERADAFAVIYLLAYLAFGVPSVIAGALVSVVGLGAVCVGYGVVVILLALVAFALRVRRAD
>NZ_CP013859.1|WP_067196416.1|1088072_1088654_-|HNH-endonuclease
MTYLSLFAMPKPVRITGRSSSITNSFVNGVIPVVPPTEEEVREALEILGMLDGIACAYCGDTSTEWDHLRPLVDMQRPTGYISEIHNLVPACGKCNQSKGNKNWLTWMRSTAPLSPTARRIADIEQRIERLQEYERRGCPTRIDFESAVGVELWERHWAHHRRILDLMREAEADAQDIRLRVREAYEAQQATD
>NZ_CP013859.1|WP_067196415.1|1086712_1087996_-|hypothetical-protein
MDDAQVGEIELITDGDGLALIGPSAAVERFLTSHGLASRDLELPRLNRAFSGSAAIAQSASEVAAQSGRWMKLTEESWAAAQKLPQVTNSSGNLQATLRAPNGQFAKNLQFVKGPGSVLTNPAMLAGAAGLMAQLAMQQTMQEITDYLAVIDEKIDDVLRAHDDAVLADMIGVDLVLDEAMTIREEVGRVSDVTWSKVQATSITIARTQAYALRRLDALAEKLETRSVNDLADVVKDVERKTQDWLSVLAHCFSLHEAVGVLELDRVFDTSPEELDRHRLALRAARTNRVELITRSTRSLLERMDAAAEVANSKVLFNPLESPAIVSARNGVNGSVGEFHTRLGIEELREGVDAKRWSRAVAETRDAALHAGGIGVNAALRAGAEGAERAARVGAEGLDKVRSLAGSVGGLAERTFRRRPGREDPVE
>NZ_CP013859.1|WP_067196413.1|1085481_1086669_-|hypothetical-protein
MASTIGWLDVSADEQRRMRELASLFTLRDSRDELGLGLLRDSIADALFPGTSTLHTRARYLLFVPWCFQHAARAKPDQRWRRLDETERSIIAPLRSSADPSGLLGERAGTALKNLPSSTYWTMLQRYGILAQPTTREDALAASAPTRLIDDDGQTTVSTIWSAPPMPPGFPAEVPDGFSLSHDEAAWLRDRVLEHAHGTLFAHLVQHRPDADSTAPWTDHAARTAPERAAGVLRQAEEFSAVMHGAQLLYNLLLAADALRFGVGDGDLVTHYRDRLDTWAQELTPAAREWRLADLLDVLRSEHEAAPAITPSTRDFIVRWSAHVRDGDPRMLLDDEAAHTLVRQRERIAKGAKARLNNPRRLATWGGASGSARLTFRWATVRGMLDDIHEGLQRA
>NZ_CP013859.1|WP_067196411.1|1083710_1085489_-|hypothetical-protein
MLEPDSRSLLSELLRPPSGFTLSHAVGTTFTLTLEAALAVPLSLAGSGASGDDAPGILSAVRRATDRIDLFAQTGYIGLGTASELVTVLEPMIHPVSMPAGRLFHPKVWFLEFASGDERRYRFVCSSRNLTTDRTWDAVVALDGHPGEAADEANDDMVRMLRWLASGGRTTPQLPGARRARLLRFAESWRSIRWEQPEHVRRFAVHVLGIGGDAPPVLDGIRSLIVSPFVTDSGLARLRARPGRPTTLVSRPEQLDRLAPASFDHLSMYVLDDFVDQALADAGTETETAQATGLVGLHAKIVVHDRAMGGSTVFLGSANATEPAWGSNVEVMVQLDGPTKQLGVDAITQSLAPLLDEYETEGGATASEDEAAERDLDSALRTIATVRLTLRVHPGEPYAASLWAADPVPVVPDGLSLSWRLLTGTDARNGTFPTAADPHLFESLALAEITPFVVVSLTDSGGRLRQSVVIAEIMDDVPGRQDAIVAAHLTQPGAFARFIRLMLQQSGPTGIADASSFSSFRSPFGGGVSEDGSGLLELLVRATATNAGALADIERVLSHLSADERSAALPAGFSEVWASVVAALDGEASRAG
>NZ_CP013859.1|WP_157540891.1|1080280_1083736_-|NUDIX-domain-containing-protein
MGRRVVRVDVDAVMRGLKGFQRDSVDHVIDRFYGPDAGSGRFLVADETGLGKSVIARGVIAKTIERLERDDAVERIDIVYICSNADLANQNLRRLNVTGDKHLAMATRLTLLARESHRLAEHDGDGKKVNLVSFTPGTSFKDGGWRSGNAEERALLCILLEHLLHPDDGEKRAMRRLFQGGVAKLSNFEWRISRMREQLGKAGPDARIAEEFSALITADGTLSRFLRLRDRVREHGTKPTTGELWHETAEVTAALRRNLAKAGVEALEPDLIILDEFQRFRALLDPSTDSEAAELADSLFTYGDAKVLLLSATPYKPFTTADDGDDDHQRDFLETIDFLAGRDAALVGDVKEALEAHRLALVTGGDASSTAASVRRALLRYMSRSERPPLARNRDMVIDRPLDGGVPSAVEIADWIALHRLDQHLGARIDIEQWKSIPYFATFMDTYKAGTRVRELLNAEGGEAVAPLLSGARGLTAEQVEQRAEIDLGNGMLRALAAETIGRGWWKMLWMPPSMPYLRPGPVYSSIGDEVTKHVVFSAWNGVPTAIAALLSHEATRLSHRGRSRSSDSSAIRLAWSLNEEGRPTQMSALALFWPHPGLASAADPLAAARAAGGAVDASFASAAVPSEGDAAEPSSAFFAFPGATPVGVEPSRLAALIGGEPDDESDAGSRFAEYLDAASAAIGAEPSGHPDLGRLAAHAPGSIAYRALRAAASPEATDIGLWRAAWELSLAFRSLFARPESAALLDTLNETDAPYWSVVLDYCADGNLQAVLDEYVFQLRSEAGGALLDDEGLMVAAQQIGAAVRMRAAAAFGHETTAARSAIRFPTRFAVRYGGSGTDADEKVAARQSGVRAAFNSPFAPFVLASTSVGQEGIDFHWWSHAVVHWNLPSNPVDFEQREGRVHRYMGHAVRKNVAAKHWGDVLASSGSAWDAAFAAAESEATDQFSPWWVYDGEARIHRRIAAFTLSRDHDKYERLLDALTLYRLTLGQPRQEDMLRLMRQNGVEAEDAGVGRGAIDLRAPRTVRVVGAVISRDGLVLAAQRGATQRLAGLWEFPGGKVELGESPTHALRREVREELRCDIIVGDRIVTTRHSYPFGTVELTTFHATVEAGEPRATEHSQLRWLGASELVSLPWADADMPTVHFLAASCD
>NZ_CP013859.1|WP_157540888.1|1079389_1080280_+|restriction-endonuclease
MSRRPLSEQQAIREDVFRWLDARRNAGAYEYSRDELINYTYNGERIPLLDTGRGIRNPADFDATLTIMTSSKKTQYSDGIGPEGLVTYSYQSREGGDNVKLRNAFDHGDPLVYFLGVRPGYFVAFYPVYIVHDDPVRREVSIALDESLRYFDDPLNLKEYERRYAERLVKTRLHQPMFRARVLRAYETTCAICNLKHAELLDAAHIVADAQIGGVAEVTNGLALCKIHHASYDQNLLGITPDYEVRIDRDLLEEVDGPMLRHGLQDMHGRPLTLPRRPADYPSKEKLAEKFALFAA
>NZ_CP013859.1|WP_067196426.1|1092320_1092617_-|DUF503-family-protein
MWIGWIEFDVLLGDVHSLKEKRSVIRPIIADLARRTEAAAAEVGAQDLHRRTAIGVSVVATHASHVRDVLDQAERMLSEQHPEVTVLSARRGLHSSDD
>NZ_CP013859.1|WP_067196428.1|1092775_1093417_+|NAD(P)H-hydrate-epimerase
MPHTVPTYTADQVRAAEAPLLAAGVPLMRRAARALAAVIAERDPKRMLVIAGSGDNGGDALFAAAELASGGTAIDVLRTSDRAHEEGFAAAMNAGAREVELDLLEPAGYDLVLDGILGIGARGALRGRARNAVQALLPHHPRVIAVDIPSGLDPDTGDTDGTVLAAETTVTFGAVKAGLATGDGPRLAGRLVLVDLGLTLADPVGSASVHAIR
>NZ_CP013859.1|WP_067196430.1|1093546_1094431_-|3',5'-cyclic-nucleotide-phosphodiesterase
MILTEHPRPSHTFVHISDTHLPGERSPLYGSGADADSNLSLLLSRLVSSGLRPDALLMTGDLTDRGDASAYRRLRALIEPAAEALKCEVVWVAGNHDSRAAMRTELLDSPSSADPITSVTWFGDLRVIALDSTVPGAHWGELDDAQLSWLAEELATPAPGGTLLLMHHPPLPTVLDLAVTVELRDQPRLAAVLRGSDVRAILSGHVHHPSFGTFAGIPVAVASSSAYGQDLAQPVGATRGQDAAQGYNLVQVYEATVVHSVVSLERGADVGEAVPADEAGRRIAGRGIGWRGQR
>NZ_CP013859.1|WP_067196433.1|1094487_1095603_-|LacI-family-transcriptional-regulator
MSPSSDAGTADAGKPDAGRPQAASADKTKADAAGRGAATPALRVTISDVAAAAGVSRATATRALKGEGRFAPETRDRILEVAERLGYVRNTMAAELAAGRTGTVGLMLRDASNPAYGLLFSRLQDEGHRRGLDLVTVTIGADEQGAKQVGALHRLLGMRVAGLIVATGGITAAQLEPFADQVPILRAGRVESSERIHTVHYDDSGHGRLLAEHILSLGHRKVVVLAGSPEASYPEHLRATAMQETLSAGGAEVTMIAAGAGPAEGVDQALSAVRVGATAVMCASDYRQLAVMRAARAAGMDVPGDVSVTGCDGILPGADLLGLTTVRIPVEEVAAAAVETMQTLLTTESPVPTVRRGFTGTLVPGTTAASP
>NZ_CP013859.1|WP_067202202.1|1095599_1097309_-|iron-ABC-transporter-permease
MLRSPLAWVTIVVVLWFAAAFLVLPNAALLGVTFFPDGQFSFRAVEKLLGSERALKTLGNSFLLAVTLSVTVNVVGVFIVLVTQYFQVRGSRLLWLGYATTLIYGGIVLAAGYNFIYGRFGFFTNLMVNVWPDLDRGWFSGYFAVVFVMTFATTTNHMLFLSSSLGKVDYASIEAAKLMGASTWTILRRIVLPVMKPMLFAVTVLTFLIGLGALTAPLVLGGPDFQTVAPLIIDLSRSPVTRDIAALLAIVLGVATIILIAVMNRAEKSGVYFSVAKVATPIQKQPIRNPVANAIVHVIAYALWVIYLIPVVLIVIFSFVDARSILAGSITFDSFTLENYITVFSSAEAIRPFLVSVVYSALASLIVVGGLLFVARLLQKHRNVVTSAIEYVLHIPWILPIVLIALALVMAFDRPQGIVANVVLTGTPVLLLIAYISVKIPFTLRLLKAAFASVPDSLEDASRILGARSLTTFRRVLIPLVLPTAAAITALNFNSLLDDYDAAIFLYHPLYKPLGVAIQESTRGENNLDAMPITFVYTVLLMIIMGVTMYLVYGRGARAGSPRRRRSRS
>NZ_CP013859.1|WP_067196434.1|1097466_1098480_-|ABC-transporter-ATP-binding-protein
MIRFDDVEVAFGDHRAVSHLDLEIQEGEFFTLLGPSGCGKTTALRTLAGFIQPTGGSIHIAGRDVTRVPSEKRGVGMVFQNYALFPSMNVRDNIAFGMSVQKVSKAERNRRVDEIAERTGLASAQLDKNVSELSGGQQQRVAIARALVLTPRILLLDEPLSNLDAKLRVQLREQLKELQHEVGVTTVYVTHDQEEALTLSDRIAVLDAGRLQQVGTPEEIYDRSATPFVCRFIGENNRLTSAQLAGIGAGLDPAAESYVRPEKLRLDAADAAASAPALDGTIVDRTYHGSHSVYTVAVADSTLRVSVPAAASARRWNPGDAVRVGVDPQWILQYPAA
>NZ_CP013859.1|WP_067196436.1|1098511_1099594_-|extracellular-solute-binding-protein
MVDIRKKRWALIGLTAAAAVALSGCAGESGDAAGTEGPDAGGSGEKIIVYTNSNSDGRGEWITEKAKEAGFDIEIVGLGGADLTNRIIAEKNNPVGDVVFGLNNMFFEQLKAEDAIEAYEPSWSGEVPQESGDPADGAYWPLVEQAIVTVYDQNRITDPPADLEELYTGTGYAGRYEVNTALGQATPQLVLASILTENLDKDGDLGVSDKGWDLVADYFANGSPAVEGTDLYARITRDEVDYGVLPSSGIAARDEEYGTKTGIIVPEYGVPYVTEQIAPIAGSGNEEQAQKFIDWFGSAEVQGEFAAEFNAMPVNEKAIEKANPEVVKLMDNLPRQDIDFGFVSEHLGDWVEKVTLEYIG
>NZ_CP013859.1|WP_083511119.1|1099931_1100858_-|NAD(P)H-binding-protein
MIVVTTPTGRVGRRLVSHLLERGSAVRVIVRDGNQLDSGIRERVDIVEGTHADERVLDRALRGAEALFWLVPPDPTAPSAEEHYLRFARAGAASIRRNRVGRVVAVTSAGHGWRGPAGLLSAAFMMDAELRATGAAFRAISLPFYMENLAGQLDGMRTRGTLSLTFAPDRPLAMVATRDIAAHAADLLTDPSWSGQQDVPLFAPDRWTPDDIARVLSEEIGSPVAYRRMSIDDFAGMLRARGAGERAIRDTVEMFAAQDQGIYDEDWKTATIAATDFRTWCREELLIGTDEHPAGARRRTGADAVLPS
>NZ_CP013859.1|WP_067202205.1|1100940_1101495_+|TetR/AcrR-family-transcriptional-regulator
MNASSRSLRADARRNRDAVLDAASELFALRGDDVQMGEIAARAGLGVGTLYRHFADKEALRAAIIGRRFEAMIAIARAAEELEDPWAAFETLLVEYLKSAEPDVAFRLAVLDRREPAWDRIAAEKDAFGEIIRRIVRRAVDAGHLRADFSAQDFILVARGAMANMSDGDDWRRHLDLMLNGIRA
>NZ_CP013859.1|WP_067196438.1|1101573_1102203_+|PadR-family-transcriptional-regulator
MNNSSFPFGGHGGSGRGGSGFGGPGFGGPGFGGAGGAASAFFEAMDQLRKSFDPRPSGGSRMARGDVRTAVLTLLAEKPMHGYQIISEIAERSGGTWKPSAGSVYPTLQLLADEGLITAEEQNGRKTYSLTEAGAAVAAEASESPAPWESTTRDGSRDHARFSALPKAGVDLAAAAAQVGRTGSPEQVQQAIDVLDDARRKLYSILAQD

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_CP013859_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_4

1254133-1254210

Orphan

Consensus_repeat	Method
GTGGGATGCCGCGGGCTGACCGT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013859_4

>merge|NZ_CP013859|4|1254133-1254210|CRISPRCasFinder
GTGGGATGCCGCGGGCTGACCGTGGAGGCGGCCGACCGTGGAGTGCGGGGCGGCCGTGGGATGCCGCGGGCTAACCGT

>NZ_CP013859|4|4|1254133-1254210|CRISPRCasFinder
GTGGGATGCCGCGGGCTGACCGT	GGAGGCGGCCGACCGTGGAGTGCGGGGCGGCC
GTGGGATGCCGCGGGCTAACCGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067196663.1\|1255792_1256170_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223317
NZ_CP013859.1\|WP_067196679.1\|1266526_1267453_+\|M15-family-metallopeptidase	unknown	unknown	gnl\|CDD\|350624
NZ_CP013859.1\|WP_067196677.1\|1265377_1266424_-\|radical-SAM-protein	unknown	unknown	gnl\|CDD\|275263
NZ_CP013859.1\|WP_067196651.1\|1246619_1248092_+\|amidophosphoribosyltransferase	unknown	unknown	gnl\|CDD\|236427
NZ_CP013859.1\|WP_067196655.1\|1251077_1251917_-\|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl\|CDD\|372574
NZ_CP013859.1\|WP_067196681.1\|1267593_1268757_+\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173849
NZ_CP013859.1\|WP_067196665.1\|1256166_1256526_+\|CrcB-family-protein	unknown	unknown	gnl\|CDD\|223317
NZ_CP013859.1\|WP_067196659.1\|1252971_1253349_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067196646.1\|1245473_1246595_+\|phosphoribosylformylglycinamidine-cyclo-ligase	unknown	unknown	gnl\|CDD\|235439
NZ_CP013859.1\|WP_067196668.1\|1258012_1258660_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225767
NZ_CP013859.1\|WP_067196657.1\|1252082_1252862_+\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133381
NZ_CP013859.1\|WP_067196675.1\|1263154_1265122_+\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223587
NZ_CP013859.1\|WP_067202266.1\|1248091_1249399_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340897
NZ_CP013859.1\|WP_067196673.1\|1261966_1262863_-\|aldose-1-epimerase-family-protein	unknown	unknown	gnl\|CDD\|185699
NZ_CP013859.1\|WP_067196670.1\|1258674_1261908_+\|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223911
NZ_CP013859.1\|WP_067202273.1\|1250451_1251081_-\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_CP013859.1\|WP_067196644.1\|1244783_1245389_-\|zinc-binding-alcohol-dehydrogenase	unknown	unknown	unknown
NZ_CP013859.1\|WP_067202269.1\|1249883_1250426_+\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP013859.1\|WP_067196653.1\|1249540_1249732_-\|DUF3073-domain-containing-protein	unknown	unknown	gnl\|CDD\|378620
NZ_CP013859.1\|WP_067196667.1\|1256654_1257800_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226609

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_067196663.1\|1255792_1256170_+\|hypothetical-protein	gnl\|CDD\|223317	COG0239, CrcB, Integral membrane protein possibly involved in chromosome condensation [Cell division and chromosome partitioning].	4.11137e-14
NZ_CP013859.1\|WP_067196679.1\|1266526_1267453_+\|M15-family-metallopeptidase	gnl\|CDD\|350624	cd14852, LD-carboxypeptidase, L,D-carboxypeptidase DacB and LdcB, and related proteins. This L,D-carboxypeptidase family includes LdcB LD-Carboxypeptidase from Streptococcus pneumoniae, Bacillus anthracis, and Bacillus subtilis, and L,D-carboxypeptidase DacB from Streptococcus pneumonia and Lactococcus lactis. These enzymes are active against cell-wall-derived tetrapeptides and synthetic tetrapeptides lacking the sugar moiety but are inactive against tetrapeptides terminating in L-alanine. L,D-carboxypeptidase DacB plays a key role in the remodeling of S. pneumoniae peptidoglycan during cell division. It adopts a zinc-dependent carboxypeptidase fold and acts as an L,D-carboxypeptidase towards the tetrapeptide L-Ala-D-iGln-L-Lys-D-Ala of the peptidoglycan stem. This family also includes vanY D-Ala-D-Ala carboxypeptidase which is vancomycin-inducible and penicillin-resistant. VanY hydrolyzes depsipeptide- and D-alanyl-D-alanine-containing peptidoglycan precursors; it is insensitive to beta-lactams. All these enzymes belong to the MEROPS family M15 subfamily B.	1.6437e-60
NZ_CP013859.1\|WP_067196677.1\|1265377_1266424_-\|radical-SAM-protein	gnl\|CDD\|275263	TIGR04470, hypothetical_protein_ALIPUT_00462, radical SAM mobile pair protein B. Members of this family are the downstream member (B) of a pair of tandem-encoded radical SAM enzymes. Most of these radical SAM gene pairs have an additional upstream regulatory gene in the MarR family. Examples of high sequence identity (over 96 percent) from cassettes in several Treponema species of the oral cavity to those in multiple Firmicutes in the gut microbiome suggest recent lateral gene transfer, as might be expected for antibiotic resistance genes. The function is unknown.	8.5654e-24
NZ_CP013859.1\|WP_067196651.1\|1246619_1248092_+\|amidophosphoribosyltransferase	gnl\|CDD\|236427	PRK09246, PRK09246, amidophosphoribosyltransferase; Provisional.	0
NZ_CP013859.1\|WP_067196655.1\|1251077_1251917_-\|DUF4097-family-beta-strand-repeat-protein	gnl\|CDD\|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	9.32997e-09
NZ_CP013859.1\|WP_067196681.1\|1267593_1268757_+\|acyl-CoA-dehydrogenase	gnl\|CDD\|173849	cd01160, LCAD, Long chain acyl-CoA dehydrogenase. LCAD is an acyl-CoA dehydrogenases (ACAD), which is found in the mitochondria of eukaryotes and in some prokaryotes. It catalyzes the alpha, beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of LCAD 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. LCAD acts as a homodimer.	1.42195e-126
NZ_CP013859.1\|WP_067196665.1\|1256166_1256526_+\|CrcB-family-protein	gnl\|CDD\|223317	COG0239, CrcB, Integral membrane protein possibly involved in chromosome condensation [Cell division and chromosome partitioning].	2.64965e-19
NZ_CP013859.1\|WP_067196668.1\|1258012_1258660_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|225767	COG3226, COG3226, Uncharacterized protein conserved in bacteria [Function unknown].	3.61159e-21
NZ_CP013859.1\|WP_067196646.1\|1245473_1246595_+\|phosphoribosylformylglycinamidine-cyclo-ligase	gnl\|CDD\|235439	PRK05385, PRK05385, phosphoribosylaminoimidazole synthetase; Provisional.	1.53201e-163
NZ_CP013859.1\|WP_067196657.1\|1252082_1252862_+\|MerR-family-transcriptional-regulator	gnl\|CDD\|133381	cd01106, HTH_TipAL-Mta, Helix-Turn-Helix DNA binding domain of the transcription regulators TipAL, Mta, and SkgA. Helix-turn-helix (HTH) TipAL, Mta, and SkgA transcription regulators, and related proteins, N-terminal domain. TipAL regulates resistance to and activation by numerous cyclic thiopeptide antibiotics, such as thiostrepton. Mta is a global transcriptional regulator; the N-terminal DNA-binding domain of Mta interacts directly with the promoters of mta, bmr, blt, and ydfK, and induces transcription of these multidrug-efflux transport genes. SkgA has been shown to control stationary-phase expression of catalase-peroxidase in Caulobacter crescentus. These proteins are comprised of distinct domains that harbor an N-terminal active (DNA-binding) site and a regulatory (effector-binding) site. The conserved N-terminal domain of these transcription regulators contains winged HTH motifs that mediate DNA binding. These proteins share the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements. Unique to this family, is a TipAL-like, lineage specific Bacilli subgroup, which has five conserved cysteines in the C-terminus of the protein.	1.40478e-38
NZ_CP013859.1\|WP_067196675.1\|1263154_1265122_+\|DEAD/DEAH-box-helicase	gnl\|CDD\|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	1.10119e-114
NZ_CP013859.1\|WP_067202266.1\|1248091_1249399_+\|MFS-transporter	gnl\|CDD\|340897	cd17339, MFS_NIMT_CynX_like, 2-nitroimidazole and cyanate transporters and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Escherichia coli 2-nitroimidazole transporter (NIMT) and cyanate transport protein CynX, and similar proteins. NIMT, also called YeaN, confers resistance to 2-nitroimidazole, the antibacterial and antifungal antibiotic, by mediating the active efflux of this compound. CynX is part of an active transport system that transports exogenous cyanate into E. coli cells. The NIMT/CynX-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.20319e-92
NZ_CP013859.1\|WP_067196673.1\|1261966_1262863_-\|aldose-1-epimerase-family-protein	gnl\|CDD\|185699	cd09022, Aldose_epim_Ec_YihR, Aldose 1-epimerase, similar to Escherichia coli YihR. Proteins similar to Escherichia coli YihR are uncharacterized members of aldose-1-epimerase superfamily. Aldose 1-epimerases or mutarotases are key enzymes of carbohydrate metabolism, catalyzing the interconversion of the alpha- and beta-anomers of hexose sugars such as glucose and galactose. This interconversion is an important step that allows anomer specific metabolic conversion of sugars. Studies of the catalytic mechanism of the best known member of the family, galactose mutarotase, have shown a glutamate and a histidine residue to be critical for catalysis; the glutamate serves as the active site base to initiate the reaction by removing the proton from the C-1 hydroxyl group of the sugar substrate, and the histidine as the active site acid to protonate the C-5 ring oxygen.	5.36804e-115
NZ_CP013859.1\|WP_067196670.1\|1258674_1261908_+\|efflux-RND-transporter-permease-subunit	gnl\|CDD\|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_CP013859.1\|WP_067202273.1\|1250451_1251081_-\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.58715e-21
NZ_CP013859.1\|WP_067202269.1\|1249883_1250426_+\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA 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 UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	6.87497e-18
NZ_CP013859.1\|WP_067196653.1\|1249540_1249732_-\|DUF3073-domain-containing-protein	gnl\|CDD\|378620	pfam11273, DUF3073, Protein of unknown function (DUF3073). This family of proteins with unknown function appears to be restricted to Actinobacteria.	4.03904e-16
NZ_CP013859.1\|WP_067196667.1\|1256654_1257800_-\|hypothetical-protein	gnl\|CDD\|226609	COG4124, ManB, Beta-mannanase [Carbohydrate transport and metabolism].	7.05075e-07

>NZ_CP013859.1|WP_067196659.1|1252971_1253349_+|hypothetical-protein
MTGPRQRSGAAFVGAAPFIVAASTYALNCALGAAVAARLVDTSGIRWVHHLLYVGTCVTTATALGLALARPGARPAALALAPAAAPLAVIPFAGTRGLRHPLVALAAAPFYIAGVVRSRSALDRK
>NZ_CP013859.1|WP_067196657.1|1252082_1252862_+|MerR-family-transcriptional-regulator
MSGRDWSIQEIARLAGTTSRTLRHYDDIGLLPPTRIASNGYRHYDENALVRLQRILLLRELGLGLPQIAEVLDRERAEASALETHLALLREEQNRLARQIASVESTIAALRGGEELMAENMFDGFDHTQYKEEVEERWGKKAYADSDRWWRGMTDAERAEWMQRAADLGRDWIATAESGVDAASDEAQALARRHVEWLTSIPGTPAATPGGDAKGYVLGLGEMYVADPRFGANYATSAGGTQGAEFVRDALRVYAEANL
>NZ_CP013859.1|WP_067196655.1|1251077_1251917_-|DUF4097-family-beta-strand-repeat-protein
MTEKWLIAPGEERVIDIENATRLKIGLVGGQVDVIGHDEPGIRIEVHGVIVKDLRIESAGGEVEIDHPQLGWDNFLEVFRNFGSGGPKAEVSVAVPRGIALNLGVVSAGALVSGIRNDARLNTVSGDIIVDTLIGDLTVNTVSGDVQVRGLTGSILANSVSGDVAVTGTVRKATVDIVSGSTLVDAAGDVNSITVNSVSGGTTVRLDESLAANYVIRSMSGRILVDGVDRGSNGPSNYTGSTGELAGRFVDLRANSVSGGVTVLRRTPATIENDPEWDA
>NZ_CP013859.1|WP_067202273.1|1250451_1251081_-|PadR-family-transcriptional-regulator
MSPAVFSHGDLRLYLLSLLAESPQHGYGIIQALTDRTGGTYTPSAGTIYPRLAKLEEDGLVTKTVDGRTTIYAITEAGRAELASREDDLAGIEAGLKDSVRLIANEVRQSVQEAMKSLRADLATAAHDERKAAKSRPRTASDDERIASREEVHRADAVINAFRARVRADLRTHVAQGGVLPASVVSQLEDALDTAAKAVTSAIAALRDR
>NZ_CP013859.1|WP_067202269.1|1249883_1250426_+|universal-stress-protein
MTDSTSEPQAEAAQNAALQKAVIVGLQPDQSRHVIDEAAKYAKLLGAPLVVVHVDVTRFVTYEDPDGYVHSAPIDINFEAGAAEFEAVQAAAADALDGTGLTWTARQLVGDPALAIKQLAGKLDAQLIVVGTRKRGIGESIREFFTGSVAARLAHRQHRSVLVVPLEEPVPDTQKEIWTE
>NZ_CP013859.1|WP_067196653.1|1249540_1249732_-|DUF3073-domain-containing-protein
MGRGRQKAKHTKIARELKSYSPAVNYSALERELGHPKDDSDSEYVDKWADEYADEDEDELERA
>NZ_CP013859.1|WP_067202266.1|1248091_1249399_+|MFS-transporter
MTSARPLWEGRAMALLGIVLVAFSLRSAVASLSPVLDHISQAFPVSPVVVGLIGAAPPVCFAVFGLLTPLVERRFGLERVAVVALALMAAGLLLRGLSVDSVTLLGATALVFAGVGSGNVLLPPLVKKYFPDRLGVMMTVYSTTMAVSTFLPPLVAVPVADSLGWRISLGMWGVFAAVALVPWVGLLIRERREPAAPVVTELLVPDPTDGVDDLRDAVAASTGPISTAPASPRIFGRLWRLPLAWALAFVFATSSSMAYASFAWMPAMLVDIGGVSPATAGFLLSVFAAVGLPCSMLVPVLVVRFQATRPLFFFAAGAGVVGLAGLLVAPRAALALWVVIFGLTAIMFPLSLVLLSIRARTPESAVALSGFVQSLGYAIAALFPLTIGLLHETTGGWQAPIVLLAAALVAAAPAGWISGRRRTIEDEWERRHGRW
>NZ_CP013859.1|WP_067196651.1|1246619_1248092_+|amidophosphoribosyltransferase
MCGIVGMVGTAPVNQDIYDALLLLQHRGQDATGIATAEANGVMHNAKAQGMVREAFRTRDMRSLLGNVGLGHVRYATKGTASSEEEMQPFYVNAPYGIILVHNGNLTNTRELTADMAQRDRRHLNSSSDTELLLNVLAGELQATTSTVDLDPERIFEAVSRTHERIEGAYAVIALIAGYGLLAFRDPFGIRPLILGRRPSTTPGAEGHDEWVVASESLVLENGDYEVVREVEPGEAVFITNDGELFTRQCAQNPTLAPCAFEYVYLARPDSIMNGISVYESRLRMGERLADTIAKHVPRDKIDVVMPIPDSSRPAAMEVARKLGIEYREGFYKNRYVGRTFIMPGQAVRKKSVRQKLNAMSTEFQGKNVLLIDDSIVRGTTSKQIIQMARDAGATSVTFASAAPPVRHPHVYGINMPSRQELIAHGRTIPEIAEELGCDYLVYQEVDDLKAAITEGSAVTDLDMSCFDGRYVTGTVTDEYLAWVEGSQSS
>NZ_CP013859.1|WP_067196646.1|1245473_1246595_+|phosphoribosylformylglycinamidine-cyclo-ligase
MAASPTNPYSEAGVDTAAGDLAVELMKSSVRATHGPEVLGGVGGFAGLFDASALLGYRRPLLASSTDGVGTKVAIAQAIDKHDTIGQDLVGMVVDDIVVVGAKPLFMTDYIACGKVVPERIADIVRGIAEACSATGTALVGGETAEHPGLLGPRDYDVAGAATGVVEADAILGADRVREGDAVIAVASSGLHSNGYSLVRHIITNAGISYADNAAEFGTTWGEALLEPTRLYTLPMLRLIDALDGGQDGGVHALSHVTGGGIAANLARVLPKGSWAEVDRSTWSPSPVFRVLSDIAGSTLESAEGTWNLGIGFLAVVAGERADAAVAALAAEGLPAWQVGTVGFGARPAGEFEEGAKGVDGGAVRLVGAYASH
>NZ_CP013859.1|WP_067196644.1|1244783_1245389_-|zinc-binding-alcohol-dehydrogenase
MSDKPQWLIREDASVPVLVALALRQTLGIRAPADLPSLRDLPVRAPDAVEASPALEAQWRDYWDMTVEPRAHRSDVPLELVDGFDTLVALPATGAEELAAAIAPHAASVLDYAHAAHDRYVSSVTSHTGGDSYRAYASAIAEFEREVGRRAHSFELNVQVLPLSQRGIWWIGALTVAVTDGLRRDVVAFDSAIRPVISELA
>NZ_CP013859.1|WP_067196663.1|1255792_1256170_+|hypothetical-protein
MAGVNLRRVFFVAVGGTVGTAARLALGMLLADAGVVPVLVANAVGAFLLGVLTARLPAATDLRLLLGTGALGGFTTYSAFMTGTLSLWADAPLLACAYAAASLVLGVGGAALGLRAGRPRAGGRA
>NZ_CP013859.1|WP_067196665.1|1256166_1256526_+|CrcB-family-protein
MTPLLFAGAAVAGGAGAVLRYLVDLGVARLAGRRFPWGILVVNLTGSFALGLVTAALPGQAVVLGAGLLGGYTTFSTAMLDTVALWRDGERPASVANAIGMLCAGLACAALGLAVGAAL
>NZ_CP013859.1|WP_067196667.1|1256654_1257800_-|hypothetical-protein
MVARPRLSRALLAAGLAAAVAAALTGAAAAASATEVSSGAGTGTASVPSATSVPRVSIRDADQTTILGWASHDLTTMASEEQAFGTTNAMLSTYVDFVQSPSFPDDDADAASARGSALLIAWEPWDWSRPADQQPEFAPRLVAAGTYDTYLTSWLTAAQERTADAEIIVRFAPEMNDSSRPWSSGTAPGATTPAEYIAMWRHVYALKQAVAPDIVMMWNPLNYGAGPYPFEDYFPGVAYVDALALDGFNWGYTAQTQAGWQSPDDVFGFTSANGPVPRLKALAGGKPWGVAETASAPDTPADFQPGGPGYGAWGTWVFQWPENPPYEATADDWITQEGWSRMLIARAEDAGASFVNFFHTVKETDWRLTDTAVGREVLTAG
>NZ_CP013859.1|WP_067196668.1|1258012_1258660_+|TetR-family-transcriptional-regulator
MSDVQRRRRDPEARRREIVAAAAELIVEIGVDALTHRKVASRAGVPLGATTQYFDTLDDLREAGVRALADEIEERIAVTRRAVVDGGVTPEVLARLIHEGLDDARAVQADRAVVTAAVHDPRVRELARFWSDEVVGFIAPVHGTDRARAAAVFIDGVLWHAQIHDEPLEERLIHDALAGILAPPTAPADSAPSADSAPFAASAPSADSAPSAASD
>NZ_CP013859.1|WP_067196670.1|1258674_1261908_+|efflux-RND-transporter-permease-subunit
MSKLAVLSLKNRALIALITIVAAVFGGIALTNLKQELIPSLELPALVVMSTYPGASPEVVENDVSTPIETAIQGVPGLESTTATSTTNASIVQATFTYGTNLATAEQKMQQAINRISSSLPEDVSPQVLSVSIDDFPVIQVAVTGFDDAENAQAELESVAIPKLEDVDGVNAAEIIGGVGQRITITPDAAKLALAGQSSQAISSALQQNGTLFPGGDITEGDQTLTVQTGAKITSVDEIAALPLVGTGLTIGDVASVVQEPDPKTSISRVDGKDALSISITKLPAANTVDVSHGVIAALDEIEEAFPDATFTIVFDQAPFIVQSIETLATEGLLGLAFAVIVILVFLLSIRSTLVTAISIPTSVLITFIGLQAFGYSLNILTLGALTIAIGRVVDDSIVVIENIKRHYVGDADKGDAIRLAVREVAAAVTASTITTVAVFLPIVFVGDMVGELFRPFAMTVTIAMVASLLVALTIVPVLAYWFLKPGKPLLDADGRAIDPEHPDAPPTPLQRGYRPILGWTLKHSGVTVALAVVVLGATLAAAPLMKVNFLSDSGQNTMTVTQDLGPTASLEAKSDAARAVEKALLDIDGIRHVQASIGSSGSALRDAFSGGAGVTYSVLTDGDADQEKLRADVQKAIDGLDDVGEVSVAASAGLGSSDIEVSVTASNSSDLEKATSAVVDELKGREGVGQVTDNLAAALPYLAVVVDRSAAAQHGLSEVAVGSIVSNTMRPQQAGSVEIDDTALTVYIAAPEPPTTAQALRELAIPTPTGIVQLQDLATVEERNGPTSITTEKGKRTATVTVPPASDNLAVATASVSAALAAVDLPAGAAATVGGVASQQADSFSQLGLAMLAAILIVYVVMVATFKSLRQPLLLLVSVPFAATGAILLQIVTGVPLGVASLIGVLMLIGIVVTNAIVLVDLVNQYREKGLSTAEAVMAGGEKRLRPILMTALATIFALTPMALGITGHGGVISQPLAIVVIGGLVSSTVLTLIVLPTLYNLVEGAKERRRARKGVGPDAGADGGRAADSGPELPGGGADAVGADADGGGADVGVAGGLPHAPQLTRRELRKRSAG
>NZ_CP013859.1|WP_067196673.1|1261966_1262863_-|aldose-1-epimerase-family-protein
MNTASPTGTQVQLRRGQVTAQIAQVGASLRALRIGDVDLIARYPLDQPTPSCSGVVLVPWPNRVRDGRWTDGDTTRQLAITEPKFGNASHGLLRFTPYEIQQTDDAAVLRAAVYPQTGYPYLLDTSVSYDLGDDGIEVTHTITNRSRTAAPVAVGTHPFVTIGDVDPHDLVLRVPAATAIDVDERMLPTGTRPADPALRDGVRLGDVTFDTGFTDLTRDDDGRVRHTLTAPDGRTLTLWQGPGFDFVQVFTTTAYPGHSLALAIEPMTAPADALNSGAGIRRLDPGETWILHWGITLS
>NZ_CP013859.1|WP_067196675.1|1263154_1265122_+|DEAD/DEAH-box-helicase
MPKNKKPRGGRPAANFEPRYGAKKTSFHDRHHGAGARPSRDGGRDERGGRTDAADRRTASAGYDRRPGSRSPGHRGYRPEPESGAPKRRWTEPESGAPKRRWTEQERAGRGEARNIRNRAESGRREAPHRRDDQGRADERPRYGERPAAGRRFDDRGGRGERGFGERPASDRPRFARDDRPRRDDRTFGGRPQRGGRDERGGQQFDRPRYADRAASGRGDRREARPSRDNWNGTPAFAPTGDVVHERLEAQAVQAVEVENVTFADLGLGSNITETLKNMGAETPFPIQAASIPAVLEGRDVLARGRTGSGKTIAFGAPLVESVLKSQAGKRREFGRSPRAIILAPTRELALQIDRTIQPIARSVGLFTTQIYGGVPQGRQVGALKKGVDIVIGTPGRIEDLVNQGKLDLSDTRIAVLDEADHMCELGFVEPVQRILRRTADGSQKLLFSATLDREVAALVDEFLVDPAVYEVAGETQETSTIEHRVLVIEHRDKAEILTSLVDREGKTLVFARTRAYAEMLAEQFDDAGIPAVSLHGDLNQAKRTRNLQRLTSGRVDVLVATDVAARGIHVDDIDLVVQADAPDEYKTYLHRAGRTGRAGRAGRVVTLITRQRQRRMGELLDRAEIDAPFEVARPGDDVIEEIAGRMPSAADLTS
>NZ_CP013859.1|WP_067196677.1|1265377_1266424_-|radical-SAM-protein
MRWQGQKLGDVDDAALPGLEDRRGVLRTVTTPEFAGMTFHEVLSKSALNKVPGASRMPFGWTINPYRGCSHACVYCFARGTHEYLDLDGGADFDSQIVVKVNVVEVLQRELRRGSWEHETVALGTNTDPYQRAEGRYKLMPGIIEALAASGTPLSILTKGTLIRRDIPLLVKAAHRVSVDVQMSIAMYDDELQKAIEPGAPTTQARLDTVRALADAGFPVTVFLMPILPHMTDSVEAITSALARIKDAGASRVIYGALHLRPGVKPWFMNWLAGARPDLVSSYRGLYPGVTVEAPKAYRQWLARRVRPLIRLHGLDGRHEDDYPVRGIRPATPSATPGSTSLAQPTLF
>NZ_CP013859.1|WP_067196679.1|1266526_1267453_+|M15-family-metallopeptidase
MNLARQPQHAPPRSPLRGPALPIGLAVTAIGVLMSLVSLPSAPADARVPPEPRVVQAVPPVDVAATTAADPCAEQVVRDAIAAADDAATIAAFGGAESFRAAVAAGNAPCIALDDPSHVWVVVNKARPLNPVDFAPQSLAPAPVRVTTGSGQARADVAAALGAMAAAAAADGVGQIGANNGYRSYDLQVRTYAGHVRSEGQANADAASARAGHSEHQTGLALDLVACAPCGGIDAFGATAQGAWVAEHAWEYGFIVRYEAGATGVTGYKPEPWHVRYIGPELAAAYHHGGFHTLEEFFGLPAAPDYLH
>NZ_CP013859.1|WP_067196681.1|1267593_1268757_+|acyl-CoA-dehydrogenase
MERDIYDEDHEAFRDLVKDFVKRHVTNDAIEKWNADGEVDRATMLAAGEAGIIGLSVPEEFGGAGMLQDYRFRAIVNEEVIAAGAGSLAGAFGIQDDLAVPYLVHMGTQEQKEKWLPRMATGEVIGALAMTEPGAGSDLRGIKTTAKKVDGGYLVNGAKTFISSGATADLVVTFVKTGEGNRPDAFSLVLIENGMEGFDHGKKLHKMGFHGHDTAELSFSDVFVPEENLIGGKEGMGFIQLMMNLPLERLSIGVAGAAAAQAALDWTVAYTKDREAFGERIIDFQNTRFKIADMAATVDALWAYIDRALLAYKDGKLSAEEAAKVKFWATEREWEVLDIGVQLHGGYGYITEYPIARAFLDARVHRIYGGTNEIMRDIVSRQIAGKR

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_CP013859_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_5

1317880-1318197

Orphan

Consensus_repeat	Method
GCCTGCGGCCCCTCAGCCGCCTGCCGC	CRISPRCasFinder

5 spacers

The CRISPR arrays of NZ_CP013859_5

>merge|NZ_CP013859|5|1317880-1318197|CRISPRCasFinder
GGCTTCGGTCCCGCAGCCGCCTGCGCCGGCTTCGGCCCCGCAACCACCCGCGCCGGCTTCCGCCCCGCAACCACCCGCGCCGGCCGCGCCGCAGCCGCCGGCCGCCTCGCTGACCGCTGCGTACCCGCCTGCCCCGGTGGCCCCGCAGCCGCCCGCGTATCACTCGCGGCTTGTTGAGCCGCAGCCTGCGGCCCCTCAGCCGCCTGCCGCCGCACCGCAGCCTGCGGCCCCGCAGCCGCCTGCCGCGTCGCAGCCGCCTGCGGCCCCGCAGCCGCCTGCCGCGTCGCAGCCGCCTGCCGCCCCGCAGCCGCCTGCCGC

>NZ_CP013859|5|5|1317880-1318197|CRISPRCasFinder
GGCTTCGGTCCCGCAGCCGCCTGCGCC	GGCTTCGGCCCCGCAACCACCCGCGCCGGCTTCCGCCCCGCAACCACCCGC
GCCGGCCGCGCCGCAGCCGCCGGCCGC	CTCGCTGACCGCTGCGTACCCGCCTGC
CCCGGTGGCCCCGCAGCCGCCCGCGTA	TCACTCGCGGCTTGTTGAGCCGCA
GCCTGCGGCCCCTCAGCCGCCTGCCGC	CGCACCGCAGCCTGCGGCCCCGCAGCC
GCCTGCCGCGTCGCAGCCGCCTGCGGC	CCCGCAGCCGCCTGCCGCGTCGCAGCC
GCCTGCCGCCCCGCAGCCGCCTGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067196777.1\|1326698_1332788_+\|fibronectin-type-III-domain-containing-protein	unknown	unknown	gnl\|CDD\|238020
NZ_CP013859.1\|WP_067196784.1\|1333802_1335068_+\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP013859.1\|WP_067196773.1\|1320497_1326569_+\|fibronectin-type-III-domain-containing-protein	unknown	unknown	gnl\|CDD\|238020
NZ_CP013859.1\|WP_083511137.1\|1298718_1299882_+\|HTTM-domain-containing-protein	unknown	unknown	gnl\|CDD\|214802
NZ_CP013859.1\|WP_067196755.1\|1313157_1314546_+\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP013859.1\|WP_067196752.1\|1312195_1313161_+\|MoxR-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP013859.1\|WP_067196737.1\|1297945_1298806_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067196781.1\|1332831_1333803_+\|MoxR-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP013859.1\|WP_067196770.1\|1319675_1320347_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067196749.1\|1306194_1312119_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380078
NZ_CP013859.1\|WP_067196746.1\|1303274_1304318_+\|NAD(P)-dependent-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|176186
NZ_CP013859.1\|WP_067196790.1\|1337463_1338726_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377640
NZ_CP013859.1\|WP_083511138.1\|1300012_1302058_+\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173839
NZ_CP013859.1\|WP_067196766.1\|1318848_1319679_+\|serine/threonine-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP013859.1\|WP_067202287.1\|1304347_1304917_+\|DNA-3-methyladenine-glycosylase-I	unknown	unknown	gnl\|CDD\|377025
NZ_CP013859.1\|WP_083511139.1\|1338722_1339535_+\|serine/threonine-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP013859.1\|WP_067196759.1\|1314542_1317104_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274855
NZ_CP013859.1\|WP_067202290.1\|1305082_1306195_+\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP013859.1\|WP_067196787.1\|1335064_1337467_+\|transglutaminase	unknown	unknown	gnl\|CDD\|376628
NZ_CP013859.1\|WP_067196793.1\|1339534_1341004_+\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|235906

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_067196777.1\|1326698_1332788_+\|fibronectin-type-III-domain-containing-protein	gnl\|CDD\|238020	cd00063, FN3, Fibronectin type 3 domain; One of three types of internal repeats found in the plasma protein fibronectin. Its tenth fibronectin type III repeat contains an RGD cell recognition sequence in a flexible loop between 2 strands. Approximately 2% of all animal proteins contain the FN3 repeat; including extracellular and intracellular proteins, membrane spanning cytokine receptors, growth hormone receptors, tyrosine phosphatase receptors, and adhesion molecules. FN3-like domains are also found in bacterial glycosyl hydrolases.	3.73197e-12
NZ_CP013859.1\|WP_067196784.1\|1333802_1335068_+\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	3.35813e-25
NZ_CP013859.1\|WP_067196773.1\|1320497_1326569_+\|fibronectin-type-III-domain-containing-protein	gnl\|CDD\|238020	cd00063, FN3, Fibronectin type 3 domain; One of three types of internal repeats found in the plasma protein fibronectin. Its tenth fibronectin type III repeat contains an RGD cell recognition sequence in a flexible loop between 2 strands. Approximately 2% of all animal proteins contain the FN3 repeat; including extracellular and intracellular proteins, membrane spanning cytokine receptors, growth hormone receptors, tyrosine phosphatase receptors, and adhesion molecules. FN3-like domains are also found in bacterial glycosyl hydrolases.	1.84032e-15
NZ_CP013859.1\|WP_083511137.1\|1298718_1299882_+\|HTTM-domain-containing-protein	gnl\|CDD\|214802	smart00752, HTTM, Horizontally Transferred TransMembrane Domain. Sequence analysis of vitamin K dependent gamma-carboxylases (VKGC) revealed the presence of a novel domain, HTTM (Horizontally Transferred TransMembrane) in its N-terminus. In contrast to most known domains, HTTM contains four transmembrane regions. Its occurrence in eukaryotes, bacteria and archaea is more likely caused by horizontal gene transfer than by early invention. The conservation of VKGC catalytic sites indicates an enzymatic function also for the other family members.	2.99815e-41
NZ_CP013859.1\|WP_067196755.1\|1313157_1314546_+\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	2.83266e-24
NZ_CP013859.1\|WP_067196752.1\|1312195_1313161_+\|MoxR-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.74299e-83
NZ_CP013859.1\|WP_067196781.1\|1332831_1333803_+\|MoxR-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.51416e-87
NZ_CP013859.1\|WP_067196749.1\|1306194_1312119_+\|hypothetical-protein	gnl\|CDD\|380078	pfam17963, Big_9, Bacterial Ig domain. This entry represents a wide variety of bacterial Ig domains.	0.000552309
NZ_CP013859.1\|WP_067196746.1\|1303274_1304318_+\|NAD(P)-dependent-alcohol-dehydrogenase	gnl\|CDD\|176186	cd05283, CAD1, Cinnamyl alcohol dehydrogenases (CAD). Cinnamyl alcohol dehydrogenases (CAD), members of the medium chain dehydrogenase/reductase family, reduce cinnamaldehydes to cinnamyl alcohols in the last step of monolignal metabolism in plant cells walls. CAD binds 2 zinc ions and is NADPH- dependent. CAD family members are also found in non-plant species, e.g. in yeast where they have an aldehyde reductase activity. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P) binding-Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	0
NZ_CP013859.1\|WP_067196790.1\|1337463_1338726_+\|hypothetical-protein	gnl\|CDD\|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	3.52379e-20
NZ_CP013859.1\|WP_083511138.1\|1300012_1302058_+\|acyl-CoA-dehydrogenase	gnl\|CDD\|173839	cd01150, AXO, Peroxisomal acyl-CoA oxidase. Peroxisomal acyl-CoA oxidases (AXO) catalyze the first set in the peroxisomal fatty acid beta-oxidation, the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. In a second oxidative half-reaction, the reduced FAD is reoxidized by molecular oxygen. AXO is generally a homodimer, but it has been reported to form a different type of oligomer in yeast. There are several subtypes of AXO's, based on substrate specificity. Palmitoyl-CoA oxidase acts on straight-chain fatty acids and prostanoids; whereas, the closely related Trihydroxycoprostanoly-CoA oxidase has the greatest activity for 2-methyl branched side chains of bile precursors. Pristanoyl-CoA oxidase, acts on 2-methyl branched fatty acids. AXO has an additional domain, C-terminal to the region with similarity to acyl-CoA dehydrogenases, which is included in this alignment.	5.76527e-167
NZ_CP013859.1\|WP_067196766.1\|1318848_1319679_+\|serine/threonine-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	5.16037e-49
NZ_CP013859.1\|WP_067202287.1\|1304347_1304917_+\|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.	2.3163e-112
NZ_CP013859.1\|WP_083511139.1\|1338722_1339535_+\|serine/threonine-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	5.01235e-57
NZ_CP013859.1\|WP_067196759.1\|1314542_1317104_+\|hypothetical-protein	gnl\|CDD\|274855	TIGR03920, T7SS_EccD, type VII secretion integral membrane protein EccD. Members of this family are EccD, a component of actinobacterial type VII secretion systems (T7SS) with ten to eleven predicted transmembrane helix regions. [Protein fate, Protein and peptide secretion and trafficking].	0.000920478
NZ_CP013859.1\|WP_067202290.1\|1305082_1306195_+\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	5.78949e-68
NZ_CP013859.1\|WP_067196787.1\|1335064_1337467_+\|transglutaminase	gnl\|CDD\|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.24225e-20
NZ_CP013859.1\|WP_067196793.1\|1339534_1341004_+\|FHA-domain-containing-protein	gnl\|CDD\|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	2.099e-08

>NZ_CP013859.1|WP_067196759.1|1314542_1317104_+|hypothetical-protein
MNARTPQQRPGAAGRQGPGAGDGLFPAPAVWGLAFVVVGVALATAAAWPLYEAPRALLVGLGGGAIGMAVAVVSRLLRWGPLLASVLAGLVYVVVAAPFAVPSSLSSPSAFLGGVRDAVLGVALGWKQILTLAPPLGEYQAVLVPFLVVVYVGAFVAALLVLDRRRRAALSVVVVAAMSVFGIAFGASATSAPLRLGGIVLPAPREWAVGVAVFLCGLVFLIGRARLERSRALRAVAAQNVSRRATPVWLRIRRHLLAGALVVVALVAGVAVAPAAAGWGDRSVLRDAVEPLVVVRQQPSPLAEYRSWFTADKLDETVVTVEGDQHGIDRLRIATLDAYDGQDFHVGADVRFSRLPRAAGPGGDRARLTLTIGDAYSGIWVPAPAHLAQAPSFAGRRADALADGFHRDEAGDTAITIAKASGGRTGLVPGDSYEVLADAPASAPSLSDAQAGEPLLDVEEHPALAEWAGMQELPRTGGGYLELIDRLRARGYLSHSLLDDEAAAGWTAELRESEGYSFAASYAGHSTARIEELFASLVEQQRRAGADASPDMLVAAVGDDEQFATAAALLARLWGFESRVVLGVRLAAAEEVPGVPACDTVCTGRNMTAWTEVREPGGAWVAVDATPQFAQLPSLITEGEQLPEHPTVPEQPRSEALDPPQAQSDSRSSDVPAEQATTDGLAAFFAIARVVGLSLAGLLLLVLPLLVILAAKCVRGRARRGAADPEVRLVAAWEELTDLYADNDVPLGPGTRVQSAEASGSAAAVRLAALVDRGVFSAHPPAAADAAQAWEVVDAERARLRKGNTWWRSLRAALGLRSFLSRLAPRSRGASSGRHLAVGTLAVAGEYRNEEDE
>NZ_CP013859.1|WP_067196755.1|1313157_1314546_+|DUF58-domain-containing-protein
MSTSHDPRLTRTAARTSTSTRTSTSTRTSTVTRYDRTRRGPVRGAVVGTRRMLRRTGRVLRRLLTWVSETVTTAGLLVSVAAVLGAAGGLAFGWVEAWAVATIAVVLLVLCVPFVLGAHDYRITLALDRDRVVAGTEIGAVLDVRNNGRRLALPGVVDVPVGDGLVEAHVPLLRPDGHHREELSIAARRRGIIDVGPMTITRGDPLGILRRELSWPEVQRIHVHPVTVPIPSTSAGLIRDLEGTPSTTLVDADLSFHAVREYVVGDSQRHVHWKSTAKTGRLMVRQYEESRHARIAIVLDLAADSYESDDEFEATVSAAASLALQGVFEGRDVLFAVSNEIPEHSRTEVLSIRALPTATPRSLLDATCAIEAGEHVMRLEAVTALTVQSYPDLSIAFLLTGSRMPLERMRHAAVTMPAAVETVAVRAELGQEPSLRNAKELSVLTLGALGDLPHMLARGVLK
>NZ_CP013859.1|WP_067196752.1|1312195_1313161_+|MoxR-family-ATPase
MTIANEQAAWFAETFSILAGNVEQAILGKRHVVELVLAAAITGGHVLLEDYPGTGKTALARSIAQTINGTSSRIQFTPDLLPGDVTGITVYDQKEGVFEFHAGPVFANIVLADEINRASPKTQSALLEVMEEATVTVDGVSRPVGSPFLVMATQNPIEQGGTYRLPEAQLDRFMIKTSIGYPDDAATMRILQGAAVPKPPLQGIAGTDTILTMGELARGVYVNPLISDYIMRIVDATRRASEVRLGVSVRGALALSRMVMTWAAKSGRTYVTPDDVRDLAVVTLAHRLVLEPEAEFDGVTAVAVIGQILLDVEPPRENGTA
>NZ_CP013859.1|WP_067196749.1|1306194_1312119_+|hypothetical-protein
MPLGDRSAPAARPRSRGRLLAVAAGVAALATVVVFAVTAQGYQAQEVPRLESSVWVLRDAGQYARVNTDLAEIDTVRDVDAPEQVWQHGAAAALFSQGSRQRWDIDPADPQDLLSEGADDGAPSASHPTPAGTRDIVAAGSYIAYRTDTGQVSVTTVEPGAATALVDPFAEVEVDEGEDPPTYTASAIGLSPDGILALYSAEEKAVRRFDIAQHRFLGDGDPVASAPEGDDALAMTVVGDRWVLLQTDEGRLWISGRGDPVDLDLGEGARLQNGVASGDSVVIADAGGLVSVALASGDSRRIAEAEGTPAAPLVMGGRTFAAWLDTDAGTLWADGDSVSLAIPDGVLESVQVEPVFRSNGDRAVLTDVATGLIWTAPDGRLIPLEQWAIDDQTEHEEGTVVVEDVAEQLPPVAVDDAFGVRAGQQVILPVLFNDHDPNKKDVLTIDPASVAGGLADAGFGELSLAGNGQTLVVTVRAESGQTSFTYAVTDGSAVSPPATVTLTVVDDEVNTAPVWCGVEACQQQWPAPQLLPGGSTIVPALSGWVDPEGDPFVLSDAYETDPAAPVMVVPLADGRVAIRHTDPNAPDATIQVTVVVADSRGAVAEKVLDVHVSASPAVVAAPVALTMRIGEPQSVRIADHLSGGSGSYRLVDAVQTAAAADGLEVSPNAASGTVDLTVAEAGQYVVTYTAQDVVTQAEKSAVIRITAVDGATPLAIMPLTAFVREGEDTTVDVLRAVQNTSGRVLLVSEAASSTPRLSVSVVGNQSVRVSGTTDDGSPGLVGTATVTVADGAGAAVKGSVTVFLAPPSSVTRPIVFPDAITVRAGALTRIDVAANDVAPRGEPLVVLPEVIGSGQPDELVFADGNSLRYLAPSTPGTYRLTYSVSLQRNPSLFDNGAVVVTVVPPGTNRAPTPATLTGRVLSGQTVTLPVPSTGVDPDGDRVVLADVDQPGAGKGTVTVSAAGDAIVYRAPAGGVDGGQVSFGYTVRDTGGEEGAGLVRIGVLDGRIDDATPVTFSDYLRVQAGSSSPVVIDPRANDLDPAQGDLELIDLVPNAPRADGNPLYERLDGLIDPATSLDDGRIVLRPGDTPGTNSYVYTVRSTRTQSTAEGLIVLTVTEESVTDQPVVSDTVVTARTRRELSEGGIDVIADRVQWASGDVSSLRLSLWGEQSGFSVSGSRIIGDPPADGALVPFQLRGVADGGREVVAYGFLHVPPFEDLRVQAVAGAEPVTVDEDGSATFDVGDYVDLAASDPFEVGTGAFGVQRAAASCTPASGKTAEYAAGRGAPWSDTCLVPVRLQGQDRWSYIEVPVGIRPAAPQVVLTSISHTVSPGQSQSIDLTGSMVSWEGGREGDPAALDYRVVYSGSSFTVSQQGSALTVEAHADAVSGTREDVTVEVGAFGGASASVRLVVGIAPPDAPRGATLTRQCVVTSPGCSIDVVGVAGEYDPFQGKPGAGLTLVSLGGGSRCDVASAAVSGERAIAVSWPGGGQAPGGQCVIPFVVADAQGRTGTGSLTLDLQGFPQAPASVTTVGYTRSTVVLEVPLGAAASAHPSVTSVTILQDGAAANASCTAAAGAVYRCTVGGLVTGAPHSFQAVAVNAVGSSAPTSAHRSWAYSPPEVSNVTATPVYRQGVTDAATGVAEIAITSSPDAASFRVQETGQVIARNGTTTKADVALSPGAQTITVVPVSQFQPPAGDIGNEGGAFTASVTVAGSVFFSPSATQAVAASNTSINVSGIAAQANGSAEPLEVVYVAWRSGDVRCTATRDGGLSVSGAEAQSSSPSIQGLAEYRLYSVKACASNGYGVAESSTVSVFTFTFVDGPGGNTTYTVDTTPKHQGDHYSYGLASEPSLTIEDGFVAQYQMYGSWRSDFTLSPDSSPGQVRARSCHATQTGSCSGAVDITATTAPTVVDVDFVPCMPVPEIDDVVTVSRAARGSYVSVVTPSVDNPGFFDVTVSWQGAFETLSPITHRMKACG
>NZ_CP013859.1|WP_067202290.1|1305082_1306195_+|serine/threonine-protein-kinase
MTAPPVLAGYSYVRPLGSGGFADVFLYEQDLPRRVSAVKVLLADAVNPEVLRTFNAEADISARLSAHPAIVTIYQASISSDGRPYIAMEYCPDNMGTRYKKGPVPVAEVLDAGVRIAGALETVHRAGLLHRDIKPSNILLSSLGSPVLADFGIAAAVVDEGDPDIIAMSVPWSSPEVLQQRVSGSVASEVWSLAATLYTLFAGRTPFEKDDRASNSRAQLTKRIVQARYTPVPLPGFPAAIDEILATAMQRDPARRFSSMAEFAERLRWAQYDLGIAPTAFEAASAEWAAAAPVSFSDSAPRGPGVTTVDAGGRRAVRAAQQRVRLEHDEPPPPRRRRPSPLMAGLIGAGVGMAALAAVGVTVLMLTGVI
>NZ_CP013859.1|WP_067202287.1|1304347_1304917_+|DNA-3-methyladenine-glycosylase-I
MNALISGPDERHRCAWVGDDAEYRRYHDEEWGTPLHGDRALFEKMSLEGFQAGLSWITILRKRPRFREAFAGFDPDVVAEFGVGDVERLMADAGIIRNRAKIEATIGNARLVREMTEGELDALMWSFAPPGPRTRPRSMADVPAVTPESTAMSKELRRRGFRFVGPTTMYALMQSAGMVDDHLEGCWRA
>NZ_CP013859.1|WP_067196746.1|1303274_1304318_+|NAD(P)-dependent-alcohol-dehydrogenase
MLRVTAYAAPSEAAPLEKTVIERRELGPHDILIDVAFAGICHSDIHTVRGDWGPQRYPLAPGHEIAGVVSAVGDAVTRHAVGDRVGVGCLVDSCGECAPCLRGQEQFCREGAVFTYGSTDRDGSVTQGGYSQQLVVSERFAVRIPDALPLDRAAPLLCAGITTYSPLRRWNVGPGTRVAVVGMGGLGHMAVQLAHALGAEVTVLSQTLSKKDDGLRLGADRYFATSDPATFRELSGSFDVILNSVSAPIELRSYLRLLDVDGALVCVGLPPEPLSLAVGGLIGGNKSIAGSNIGGIAETQEMLDFCAEHGIAAEIEVIPASEINAAYERVLASDVRYRFVIDAATFA
>NZ_CP013859.1|WP_083511138.1|1300012_1302058_+|acyl-CoA-dehydrogenase
MVDVATAPEVKNPKLDGERITALLLGTWADTRRQAREMIKDPAFWRNDDLAKDEHRERVLSQLHLLVENRAVHRAFPKRFGGEEDNGANIAGFEELVAADPSLQIKSGVQWGLFGSAILQLGTTEHHDKWLPGVMDLSIPGAFAMTEIGHGSDVASVGTTATYDPETEEFVIHTPFRGATKEYLGNAALHGVAATVFAQLITNGVNHGVHCFYVPLRGEDGTDLPGIGREDDGLKGGLNGIDNGRLSFDHVRIPRTNLLNKYGDVAPDGTYSSPIDSPGRRFFTMLGTLVQGRVSLDGASSWASALGLKIAITYANERRQFDGADGQEVVLLDYGKHQRRLLPRLATTYAQIFAHDEFLQKFDGVFSGRTDTPDDREDLETLAAALKPLSTWHALDTLQEAREACGGAGFMFENRLVGLRADLDIYVTFEGDNNVLLQLVGKRLLTDYAAQFKGKDAAALAKYAVGQTAGKVFHGAGLRQLGQAVADLGSTARSVEKGLREEQQHELLADRVQQMIADIAGRLRAAGKDKALGARLFNENQAELIEAARAHGELLQWEAFTDAVHRVDHGDTKKVLTWLRDLFGLQLIEKHLAWYLINGRLSTQRAAAVSSYIDRLCARLRPYAQELVDAFGYEPEHVRAPIASGAEKARQDEARAYYAELAASGEAPIQEKALKKGAARG
>NZ_CP013859.1|WP_083511137.1|1298718_1299882_+|HTTM-domain-containing-protein
MASADRGGGPEPRELREHVPQPVREDPEVTSERTASLPTRLLAFAASMIAGFWAMVLSAVERISAFVSDWLWNGKKSLYGLAVTRILFGVTALGLLAANFGTRLYTFGSGSAWNGELAEPVSDFPKIWVFSAFHAAMGNDVVYTLLYLLLAALAVLFVLGWRFRIVLPVFFCLWVGFIEANDMVGDQGDNMFRIALLLLFFADPAARWSLDARRRAKSGEWFAPGSQPALLGTVFHNLALVALTAQVCFVYASGALFKAGGVPWKEGYAVYNPLHTMRFGTWPVLSDLVTTWGPMVTMMSWGSIILQVAFPLALLTRPTRLIALIGILSFHIGIAVLMGLPWFSLTMIAIDSIFIRDRTWRRLSAGVVRRWQAAKAVAPPTPDRAAV
>NZ_CP013859.1|WP_067196737.1|1297945_1298806_+|hypothetical-protein
MSTMTDTAPTDEDVPAAQTDPAAQTAPAAQTDPAVRPRPAWWAKLIAFAAVLLTLWHVFASFLWIAPYSALREIPTQEVLAGYMLPMFGQSWSVFAPEPINGDYHFNVRAVIEKDGEEVETGWVSATDVELSMIRYNLFPPRAGIQSSEVASGQMNAYNKLNEEQQAVVALDFDKDDWEDWMVRTFDKLEGDDKPSTDAYMAEEHMATAYATQVAYAIWGADAVIKVQYRVSRQNVVPYAQRNEPDAKRPDPTFSTTGWRLPIEEEGQSRENFANTFRSQFERIQK
>NZ_CP013859.1|WP_067196766.1|1318848_1319679_+|serine/threonine-protein-phosphatase
MTLSSVILNVASLTDVGLTRAVNEDSVLAASPVFLVADGMGGHDAGDRASQAVVEAFQPLGGHEVSTADIGAALARANGAVSAISAQHARGAGSTVAAVALIEHEGVPHWLVFNVGDSRVYRHHDTELDQLTIDHSLGQELVDAGELRAEDMATFAHRNVITRAIGAEENLADSWLVPVIDGDRLLICSDGLSGEVSDESIRATLTMCGRPETAAAALVRRAKQAGGRDNISVIVIDVVAGGAAPPSADGTDSRQSAVHTTTMLESTTVPVRGRSS
>NZ_CP013859.1|WP_067196770.1|1319675_1320347_+|hypothetical-protein
MTGHEGIDDETVVLSRRALRRRAESAPTQGTQDEHSDAVEHVDGLDERTVVMDRSARPADAAPDGHADGLDERTVVMDRSALPSDAVPARETDDSTMVDDSTVVVDRTVVVDRTVVADRSRARREPRGNAPDPLHDTVRVVRAPAPAAPETPAIYKPRAAPRVPSAPPAVANDIPPTRTADASAPSVARTSRRRSVYALAAIGAAGIVSIAGLALLVGVAVTS
>NZ_CP013859.1|WP_067196773.1|1320497_1326569_+|fibronectin-type-III-domain-containing-protein
MKALSWMRMKPKTLASSAAVTVGAIAITTMAFAYEGNPTTKVDLNDGGVWITKTSSLLVGHFNHESTVLDGGLRNGSDDYDILQDAAQVLVVDDSASTVTAVDPARVALTDSAAIPGSAKVALGNRTAAILDRDSGDLWVVPVSGIAAFEIKGTDPTVELGEHADVAVAKDGTVFGLSAQRGEVVTIPVDNQGEALDASTASIGEVDPAGDPSITAVGDAPVVLDPAAGAVVTPGGTRTEIGDADGALLQQPSAETDAVAVATASALVRVPLDGGEPQKIDAGGVGAPAAPVWLRGCTYGAWAGSASFVRECPGETNDVAEKIPDAEDSTSLVFRVNRDVIVLNDAVGGAAWLPNESLQRVDNWDDIVPPEGENENQEDTTEETVETTLPERSEQNTPPIAEDDEFGVRPGRTTMLPVLDNDTDADGDVLVASLAQSQPALGEVQPVNNGGSMQIAVDEDTTGGGSFEYQVDDGRGGKATATVQLTVHDWETNGAPEQRRTTGIAVEEGGSVSYNVLPDWLDPDGDDIYLRNVVAAPGDEVDFTTDGQVTYRAVASLQGRKDIQVTVADGLGETATGTLRLDVRPAGSTMPKTNADHVVTRVGEAISVSPLVNDTSSSREPLRLARVDEVPGATIVPDYQNKAFTFRSETAGVYYAQYLVSAGPNAVPGLVRIDVLPPSETQLPPIAVRDVALLPSGGEVLVGVLGNDTEPSGGILVVQSVTVPPHSGISVSVLNHETLRIGDQGALSEQVRISYRISNGTQSAEGDVIVIPIPRPEQLLPPVANDDQVVVRAGDVVTIPVLDNDTHPNGDVLHVDPQLVEPLVDPEDGEAFVSQDTVRFRASDRPGTVYLTYQAVDSMGQKDAGYVTVQVRPVDEESNSAPKPQDLTVRALSGSSVRIAIPLDGIDADGDSVELVGQESAPSKGQVAEVGTNYLVYEAFDDAAGVDSFTYRVRDRLGKEGVATIRVGIAPGDSANQAPYAVKDAVVVRPGRTIAVPVLANDSDPEGDAISLVKKGLEIPSDAGLQARVSGDRVVVKAPDRTMDTSIQYTIRDARGATATAVLQITVDDEVPLKVPTARDDRVVAADVTDSLRVDVDVLTNDEDPDGTVDALDLTVETGGVVQEDRSIRVTVGEQRQLIRYTVTDQDEQSASAFIFVPALSELRPTLSSTKPVEVKSGETIELPLSKYVTVAGGGDVVITEAAKVSAVNSDGSPLIKDQTTLVYTSKPGYFGKDALTFEVTDGTGPDDPQGRKATLTIPITVLPPENQPPVFVNGQVEVAPGEPATSLDLAALTTDPDPEDADKLRFRISGEPGNGISARVDGSKLLVEAGSSTPKGTSATVQLRIDDGTTEPVEGSVAVLVTASTRALPTANTDTIAEADQGKTITVPVLQNDVNPFPETPLKVVSVVPETGSGTAEISGSEVKVTPSADFVGTFVVRYRVQDATKDPDREVDGRIVLTVQGVPEAPGTPTVSSVQDRTVVLAWSPPANNGAEITSYTVRSVAGNYTKKCSSTTCTLDGLTNNVEYVFQVVATNRVGDSEPSPSSAVARPDARPDTPQPPKLVFGDKSLKVSWATPTTPGSPVESYTLEISPAPPSGVAQKTGVTGNSLVWEGLENGADYQVRVRAHNRAPEPSSWSGWSASEIPAGVPGTVAAPRAQSAPSVGSQAQMTVSWDAAPQNGDAIAEYELLVMRGGSIVNRVPRIAGTQHSQTVTVATSTADYTYAVRARNKAGWGAQSPASTPQRAFGSPGAPTITGAQEHDGYVTVQYSLSDTNGANSSEIHYEYTLDGSTWSRNWDGERINAANNGTYTVRVRAYSVVGGQESQPGPASAPSGALRPYGPVANPGVGAANQGLSVKVSWSAPAPNGRPIEEVQVRLDGGSWQNLGLSGSRNVGNGYDQTHTIEVRARDSAGQWSNVVSASARTDSKPQPDAWVTGGSYVSGCTNVGGGTCRKFVLNTSNFAGGSYNIECTVDGRVFGNNAGFPVDIPSNGSVQLDCYNGFGTSKGVNIIGGNPSKARPGNF
>NZ_CP013859.1|WP_067196777.1|1326698_1332788_+|fibronectin-type-III-domain-containing-protein
MKALAWMRARPKTLASAAGVAAGAVVLTGMAFLYEGNPTTKVDLNDGGVWITKSSSLLVGHFNHPSALLDGGLRTTGEDFDILQDETAVLVVDSAASTLTAVDPARVSLGDSAGIPPGAKVSLGNRTAAIVDRTSGDLWVVPVGGIASFTVESAEPVAELGKDADAVVADDGTVFGLSAERGEVVTVSVDAEGEALEPSTASVGELSSSQRPSITAVGRTPVVLDAGAGEVVVPGGARTAVPDAADAVLQHASAATDAVAVATPSALVRVPLDGGEPEVIETSGRGTAAAPVWLRGCTYGAWAGSARFLRDCPGEQSDVDARIEGAESSATLTFRVNRDVIILNDAVGGSAWLADESLQQVDNWNDITPPEGQTENEEDTAQETVETTLPERKPENTPPVAEDDSFGVRPGASILLPVVDNDNDPDGDVLVAALAEQQPSIGTVQPIQNGGALQIAVDEEATGSDTFTYEVDDGRGGTDTAVVTLAVHEDDVNAAPTPKRKTTLTVETGGTISYNVLPDWIDPDGDDIYLKEVIPAPGDEVDFSTDGQITYKATASLQGRKEIQVTVADGFNEMQSASVTLDVRPQGSTAPKTNADHVVTRVGEQVTVAPLANDTSSGREPLRLGRVDDQVPGATVLPDFPNKSFTFSSDTPDTYYVQYLATAGPENAEGIVRVDVLEAAETELPPVAVRDVALLPSGGDVLVGVLANDSDPSGGILVVQSVSLDQGTGISVSVINHETLRITDQGALDSQVRVRYRISNGSQSAEGEVVVIPIPAPEKILQPVANPDTATVRAGDVVTIPVLENDTHPSDDVLHVAPELVEPLVDPEDGEAFVSQDTVRFKAGPEPKTVYLTYDAVDSRQQKSAGFVTVQILPVEEGKNAAPRPRDLVARALAGTEVSIAVPLDGIDADGDSVELLDIASNPTKGRITDTGQNYFTYEAFEDSTGVDTFEYRVRDRLGKEGTATIRVGIAPAEDVNREPYAVKDAVVVRPGREIAVPVMANDSDPEGDEISLVSEKEGGLEIPDVDGLSARVSGDRVLVQAPNRSLETSLQYTIRDSRGATATAVLQITVDDEVPLVAPVARDDRVRPEDLNEGSLTADIAILENDEDPDGTTDSLTVTLGDGATALENGMVRVAITDELQLITYTLTDQDGLSASAFLFVPAKSGLRPVLSSTKPVEVVSGETKELPLADYVTVAGGGTARITEHAKVAAVHADGSDLVKDETTLVYTSAQGYFGEDAITFEVTDGSGPDDPDGRTATLSLPITVLPPANQQPVFTGAEMQVAPGEEATRLDLAALTADPDPEDAGHHSYTLVGGAGKGVSARIDGDDLLVEASSNAKKGTVLSLTVRVTDGETEPVEGQVSVVVSASNRALPVANTDTVSEADQGKPVTVSVLDNDFNPFPETPLRVTSAVLETGAGDVTVKGDTVEVTPGATFVGTMVVRYRIQDATEDVDREANGQVVVTVQGVPEAPGTPTVTSVQDRTVVISYSAPSNNGAEITAYTVRSVQGSAYTKTCQSTTCTLDGLANNVEYTFQVTATNRVGEGKPSGVSDVARPDARPDTPSPPTLTFGDRSLTVKWATPSTPGSPVESYTLEISPAPPSGVSQKQATGNSLVWDGLENGANYQVRVQAHNRAPEPSSWSGWSASEIPAGPPLDPAAPTTAELAPVGDQAQMQVNWVPPNPNGDAIDSYQLEVYEGSTLVRTVTPGAGARSQAVVVPTSESAYTYRIRAHNKAGWGAWSPQSAPRRGVIAPGAPTSVSVVKEMDRALQITYTPGSRNGARTSEIAYQYRLGAGGWANLPGDNIIGGLTNGQDYDVSLRAVATVDGVQYSGAASNSARGNPYGPLKPPTVGASSNARSVTLSWNGEVSANGRSITKVETSIDGGGYRSASSTGSQTVGDGYSEQHSIRIRVTDAAGQVIESTTASATSGPAPQPKAWTTQGADSGECSPDVCYYLGFSVSNFPAGEYTVWCLEDGKRFAGGATWVVPANGAAYKKGPGGCYHGGFNSRYLLQMEIVGWGVTEGIRWD
>NZ_CP013859.1|WP_067196781.1|1332831_1333803_+|MoxR-family-ATPase
MTMTPEQAAWFQGTFTRLVDNVDKAVKGKREVVSLVLASMLAEGHVLLEDAPGTGKTSLAKALAATVQGTSARIQFTPDLLPSDVTGVTIYDQQSHRFEFHRGPIFASIVLADEINRASPKTQSALLEVMEESRVTVDGVTHDTGRPFLVIATQNPIEQAGTYKLPEAQLDRFLIKTSIGYPDLDVTESILAGASDRNPAAGLPAIITTSAVADMADLGSTVHVEPAVLRYVAELAEATRADAGVRLGVSVRGAIAMVRIAKIWAAAHGRHFVLPDDIKALARPVWQHRLLLDAEAEFAGTTSDVVVARVLEAVAAPQARTAA
>NZ_CP013859.1|WP_067196784.1|1333802_1335068_+|DUF58-domain-containing-protein
MTTEALQTAQTAPAEPSAGWRDVAAVVGARVLARLRLIASAIRPLAWVLMALAVAFWILGQTAGWAEFTIAAVVVAITVAVCALFLVGRTAYDVSLDLARTRVVVGERAVGALTLANRGTRAILPSRVVLPVGSGRGEFGIQRLAPGEEAEELFAIPTHKRGVVKVGPVSVVRGDPLGLFERAHRRDDPVDLFVHPKTVLFDGQSLGYLRDLEGLPAADLSRDDVSFHALLEYQPGDDLRHVHWKSTARTGTMMVRQYEETRRSHFVIGLSRSSGDYATDDDFELGISIAGSIGLRAIRDSQRVDVRVQGRALAAGTGKQLLDSLAAIEHSRPRDGGIGDLAGVVARTMPLASVVVLVCGSRVGADDLRLACSRLPFGARVIAVVADRSAAAPALRRIGDADVVTIGSLEQTPLALLKVLS
>NZ_CP013859.1|WP_067196787.1|1335064_1337467_+|transglutaminase
MTSTVPERTTLPLRRWVLDIGVSALLIGVSIAGFWPTFAGPSYLLAAVGGLVLGLAIAAVAAWRRWGILVIAGLTVAAYFVFGGALALPQTAIAGVVPTLDTLQRLALGTVTSWKQLLTTVAPVSTADGHALVPFLLSLLSAVITASLALRLSHVGWALIPAGAMLVLTIALGTPEPAFPVAQGLLFAVLSIAWMALRQLWAPQNAAVSVGEVDPSRAAHMRMRRLLAGVAVLAVAGGAGVAGSAIAAPAQPRHVFRDVIIPPFNIRDYPSPLQSFRKNVRDNAEDTLFTVRGLPEGARMRIAVMDQYDGMVYNVTDGGPESSSAFTPLRSNMAPDAEGIPVSLKVEIEKYSGVWVPDAGAVSEIDFTGDRAEELRRSTYVNTETGTAVATSKLRSGDAYTVDTVMPAEIEDSQLADADFGKVALPKQSNVPEELASLAAETVAGAETPIEQVRALETFFAEGGFFSHGLEGEVLSRAGHTAERISTLVGGDQMIGDDEQYAVAMALLAREVGIPARVVMGYYPDEEDADDAEFAATGDDVHAWVEVNFEKFGWLPFNPTPPEDKVPNDQNTKPKVDPKPQVLQPPPPPQEPVDLPPTLPDDRKGEDESLNILGILGVILAVGGISLAIIALLASPFIVIGAWKAARRRSRRNAARASDRISGGWNELTDRAVDYGARIAPGGTRAEEAVTVASTLTLPEVTALAARADSEVFGPDEPTPEDVEAFWAEVDGIVGGLGKEAGFWKRMKARLSLRSLLGGTAIAGGLQSLRDAAAARVRREPGTIESSTDTTSTSAESEAS
>NZ_CP013859.1|WP_067196790.1|1337463_1338726_+|hypothetical-protein
MTTVAFDSMAPISRRAIAYLIDALIAGGIAVVGTIVLAVVAAMTRPIENLLIVLPVGYGVLLLVLLAWLLVYTRMQVGGGSIGMRAQGVRLVSTDGTPLGYGRALLRNVIFGLAAGIVVGYFTPLFDGSGRFQGWHDKVAGSLVVDARRAAPPSDAAPATSAMPVAAPASSPAAQPTIPGIPVPSPAASFAPPVPPVPPVPPVQPTPAPAAGAPTVDTTIPAASAAPVVDPASSAPVPAAPVAAEGSVIAYVPGVSRPEPAAPAQPAGPAGHAPEPAAPVAASAPPVPASAPPVPASAPTAADDIEDTRISIPGHRLVFTWDDGTKVPVSRRTIFGRNPAPEDGAVLMPVRDETLSLSKTHFEAAADTSGGWVLDRHSTNGTTIVRDGQRIACPPGQRVPVRLGDAIEIGDRIVTIGGYA
>NZ_CP013859.1|WP_083511139.1|1338722_1339535_+|serine/threonine-protein-phosphatase
MRPGLIVSSGSATHPGLRRALNEDAFLASAPVFIVADGMGGHEAGERASATVIEEFAFYIGRTALELDDVRAALERAREGVEHLSTSGNGRAGTTLSGVVIASVDGMGYWLALNIGDSRTYRLADGELEQITVDHSVVQELIESGELTPEEAATDRRRNIITRAIGASSTGDADYWLFPAERGDRILVCSDGLTAELTDARIREILATTPDPQQAADALVSDALGAGGRDNITVVVADAVSVASRPGTLLDTETHIDMDTRPREAAGGVR
>NZ_CP013859.1|WP_067196793.1|1339534_1341004_+|FHA-domain-containing-protein
MQTIYRPGEWYLIVIPGALVALPPDVPGEVVARLWDRLPAEKTLATVIDVLTTQAGGSFAALPPFAAAVAEGADVRLALRGGVAARVSGGTDAAQDYSGSEVTTWSERFVGGATRVEITVEESDAASALPVQSGVVRAAAVSAELEAGDADPLVAVLGPAPLLEQSATTGFSAAALAGAVAPPLARFGTRGDAASLDSVEQDESVEPAVPAEPDAPGGTAAAESVDPAADAAADDAVAAPEPPDEPAPVDEPAPVDEPAPVDEPAPVDEPASVDEPAPADEPADSAEHDALLDEGITLIPTETLAPLSEEDEFEQLFGETVHSASSVGVPPPPPLPGAVQGDHDGATISSAQLRALRQQPPVGDDAPTAVLPVVSGSVGRIRFSTGQVVTLDRTVIIGRRPRSTRASGENLPHLVAVESPQQDISRSHLEVRPEGDTVVVIDLHTTNGSTLLRPGADPVRLHPGEQTLVLSGDVVDLGDGVTLVFEDLP

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_CP013859_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_6

1895159-1895239

Unclear

Consensus_repeat	Method
CCCGCGGCGGAACGCCGAAGCGC	CRISPRCasFinder

1 spacers

cas3

The CRISPR arrays of NZ_CP013859_6

>merge|NZ_CP013859|6|1895159-1895239|CRISPRCasFinder
CCCGCGGCGGAATGCCGAAGCGCCTCCATGCCGTCGGGCCCGTCCGCGCCGGAGAGCGCACGCGGCGGAACGCCGAAGCGC

>NZ_CP013859|6|6|1895159-1895239|CRISPRCasFinder
CCCGCGGCGGAATGCCGAAGCGC	CTCCATGCCGTCGGGCCCGTCCGCGCCGGAGAGCG
CACGCGGCGGAACGCCGAAGCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067197986.1\|1884501_1884855_-\|Fe-S-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067202469.1\|1890226_1893772_+\|transcription-repair-coupling-factor	cas3	cd09639_cas3_CAS-I	gnl\|CDD\|224118
NZ_CP013859.1\|WP_083511342.1\|1896805_1899538_-\|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl\|CDD\|234570
NZ_CP013859.1\|WP_083511183.1\|1901554_1902823_+\|histidine--tRNA-ligase	unknown	unknown	gnl\|CDD\|273080
NZ_CP013859.1\|WP_067198012.1\|1900770_1901520_+\|MazG-family-protein	unknown	unknown	gnl\|CDD\|237065
NZ_CP013859.1\|WP_067202472.1\|1902891_1903686_+\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238874
NZ_CP013859.1\|WP_067197983.1\|1883096_1884497_+\|sugar-kinase	unknown	unknown	gnl\|CDD\|212662
NZ_CP013859.1\|WP_067198009.1\|1899590_1900757_+\|Na+/H+-antiporter-NhaA	unknown	unknown	gnl\|CDD\|377746
NZ_CP013859.1\|WP_067198005.1\|1895306_1896674_-\|NADP-specific-glutamate-dehydrogenase	unknown	unknown	gnl\|CDD\|181834
NZ_CP013859.1\|WP_067198001.1\|1889567_1890131_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379112
NZ_CP013859.1\|WP_067197999.1\|1888617_1889481_-\|Fpg/Nei-family-DNA-glycosylase	unknown	unknown	gnl\|CDD\|223344
NZ_CP013859.1\|WP_067198017.1\|1903666_1904179_-\|glyoxalase	unknown	unknown	gnl\|CDD\|319910
NZ_CP013859.1\|WP_067198022.1\|1905036_1906272_-\|APC-family-permease	unknown	unknown	gnl\|CDD\|129987
NZ_CP013859.1\|WP_067198019.1\|1904253_1905036_+\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|378964
NZ_CP013859.1\|WP_067198003.1\|1894477_1895074_+\|gamma-carbonic-anhydrase-family-protein	unknown	unknown	gnl\|CDD\|223735
NZ_CP013859.1\|WP_067197992.1\|1885410_1886673_-\|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|181774
NZ_CP013859.1\|WP_067197989.1\|1884940_1885414_-\|6,7-dimethyl-8-ribityllumazine-synthase	unknown	unknown	gnl\|CDD\|234606
NZ_CP013859.1\|WP_067197995.1\|1886669_1887299_-\|riboflavin-synthase	unknown	unknown	gnl\|CDD\|236455
NZ_CP013859.1\|WP_067197997.1\|1887298_1888342_-\|bifunctional-diaminohydroxyphosphoribosylaminopyrimidine-deaminase/5-amino-6-(5-phosphoribosylamino)uracil-reductase-RibD	unknown	unknown	gnl\|CDD\|273015
NZ_CP013859.1\|WP_067198024.1\|1906336_1906807_-\|DUF4442-domain-containing-protein	unknown	unknown	gnl\|CDD\|373120

Protein	Function_ID	Function_description	E-value
NZ_CP013859.1\|WP_083511183.1\|1901554_1902823_+\|histidine--tRNA-ligase	gnl\|CDD\|273080	TIGR00442, hisS, histidyl-tRNA synthetase. This model finds a histidyl-tRNA synthetase in every completed genome. Apparent second copies from Bacillus subtilis, Synechocystis sp., and Aquifex aeolicus are slightly shorter, more closely related to each other than to other hisS proteins, and actually serve as regulatory subunits for an enzyme of histidine biosynthesis. They were excluded from the seed alignment and score much lower than do single copy histidyl-tRNA synthetases of other genomes not included in the seed alignment. These putative second copies of HisS score below the trusted cutoff. The regulatory protein kinase GCN2 of Saccharomyces cerevisiae (YDR283c), and related proteins from other species designated eIF-2 alpha kinase, have a domain closely related to histidyl-tRNA synthetase that may serve to detect and respond to uncharged tRNA(his), an indicator of amino acid starvation; these regulatory proteins are not orthologous and so score below the noise cutoff. [Protein synthesis, tRNA aminoacylation].	7.26866e-96
NZ_CP013859.1\|WP_067202469.1\|1890226_1893772_+\|transcription-repair-coupling-factor	gnl\|CDD\|224118	COG1197, Mfd, Transcription-repair coupling factor (superfamily II helicase) [DNA replication, recombination, and repair / Transcription].	0
NZ_CP013859.1\|WP_083511342.1\|1896805_1899538_-\|phosphoenolpyruvate-carboxylase	gnl\|CDD\|234570	PRK00009, PRK00009, phosphoenolpyruvate carboxylase; Reviewed.	0
NZ_CP013859.1\|WP_067198012.1\|1900770_1901520_+\|MazG-family-protein	gnl\|CDD\|237065	PRK12334, PRK12334, nucleoside triphosphate pyrophosphohydrolase; Reviewed.	1.90823e-67
NZ_CP013859.1\|WP_067202472.1\|1902891_1903686_+\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238874	cd01836, FeeA_FeeB_like, SGNH_hydrolase subfamily, FeeA, FeeB and similar esterases/lipases. FeeA and FeeB are part of a biosynthetic gene cluster and may participate in the biosynthesis of long-chain N-acyltyrosines by providing saturated and unsaturated fatty acids, which it turn are loaded onto the acyl carrier protein FeeL. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	3.99108e-48
NZ_CP013859.1\|WP_067197983.1\|1883096_1884497_+\|sugar-kinase	gnl\|CDD\|212662	cd07779, FGGY_ygcE_like, uncharacterized ygcE-like proteins. This subfamily consists of uncharacterized hypothetical bacterial proteins with similarity to Escherichia coli sugar kinase ygcE , whose functional roles are not yet clear. Escherichia coli ygcE is recognized by this model, but is not present in the alignment as it contains a deletion relative to other members of the group. These proteins belong to the FGGY family of carbohydrate kinases, the monomers of which contain two large domains, which are separated by a deep cleft that forms the active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain.	1.07592e-105
NZ_CP013859.1\|WP_067198009.1\|1899590_1900757_+\|Na+/H+-antiporter-NhaA	gnl\|CDD\|377746	pfam06965, Na_H_antiport_1, Na+/H+ antiporter 1. This family contains a number of bacterial Na+/H+ antiporter 1 proteins. These are integral membrane proteins that catalyze the exchange of H+ for Na+ in a manner that is highly dependent on the pH.	8.77898e-104
NZ_CP013859.1\|WP_067198005.1\|1895306_1896674_-\|NADP-specific-glutamate-dehydrogenase	gnl\|CDD\|181834	PRK09414, PRK09414, NADP-specific glutamate dehydrogenase.	0
NZ_CP013859.1\|WP_067198001.1\|1889567_1890131_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	3.93611e-32
NZ_CP013859.1\|WP_067197999.1\|1888617_1889481_-\|Fpg/Nei-family-DNA-glycosylase	gnl\|CDD\|223344	COG0266, Nei, Formamidopyrimidine-DNA glycosylase [DNA replication, recombination, and repair].	5.60295e-54
NZ_CP013859.1\|WP_067198017.1\|1903666_1904179_-\|glyoxalase	gnl\|CDD\|319910	cd07246, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	3.88165e-26
NZ_CP013859.1\|WP_067198022.1\|1905036_1906272_-\|APC-family-permease	gnl\|CDD\|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	2.01992e-39
NZ_CP013859.1\|WP_067198019.1\|1904253_1905036_+\|AraC-family-transcriptional-regulator	gnl\|CDD\|378964	pfam12833, HTH_18, Helix-turn-helix domain.	8.30755e-22
NZ_CP013859.1\|WP_067198003.1\|1894477_1895074_+\|gamma-carbonic-anhydrase-family-protein	gnl\|CDD\|223735	COG0663, PaaY, Carbonic anhydrases/acetyltransferases, isoleucine patch superfamily [General function prediction only].	2.48123e-38
NZ_CP013859.1\|WP_067197992.1\|1885410_1886673_-\|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II	gnl\|CDD\|181774	PRK09311, PRK09311, bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II.	0
NZ_CP013859.1\|WP_067197989.1\|1884940_1885414_-\|6,7-dimethyl-8-ribityllumazine-synthase	gnl\|CDD\|234606	PRK00061, ribH, 6,7-dimethyl-8-ribityllumazine synthase; Provisional.	3.04546e-53
NZ_CP013859.1\|WP_067197995.1\|1886669_1887299_-\|riboflavin-synthase	gnl\|CDD\|236455	PRK09289, PRK09289, riboflavin synthase.	6.18029e-100
NZ_CP013859.1\|WP_067197997.1\|1887298_1888342_-\|bifunctional-diaminohydroxyphosphoribosylaminopyrimidine-deaminase/5-amino-6-(5-phosphoribosylamino)uracil-reductase-RibD	gnl\|CDD\|273015	TIGR00326, eubact_ribD, riboflavin biosynthesis protein RibD. This model describes the ribD protein as found in Escherichia coli. The N-terminal domain includes the conserved zinc-binding site region captured in the model dCMP_cyt_deam and shared by proteins such as cytosine deaminase, mammalian apolipoprotein B mRNA editing protein, blasticidin-S deaminase, and Bacillus subtilis competence protein comEB. The C-terminal domain is homologous to the full length of yeast HTP reductase, a protein required for riboflavin biosynthesis. A number of archaeal proteins believed related to riboflavin biosynthesis contain only this C-terminal domain and are not found as full-length matches to this model. [Biosynthesis of cofactors, prosthetic groups, and carriers, Riboflavin, FMN, and FAD].	8.14301e-93
NZ_CP013859.1\|WP_067198024.1\|1906336_1906807_-\|DUF4442-domain-containing-protein	gnl\|CDD\|373120	pfam14539, DUF4442, Domain of unknown function (DUF4442). This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 139 and 165 amino acids in length. There is a conserved PYF sequence motif. There is a single completely conserved residue N that may be functionally important.	6.91251e-12

>NZ_CP013859.1|WP_067198003.1|1894477_1895074_+|gamma-carbonic-anhydrase-family-protein
MLYEHLGARPRIHDTAVVAPTAVVSGDVEIGPHCQVLHGAVITAEGGPITLGEHVIVMENALIRATAANAVHIGAHTLVGTLASIAGATVGEEVFFASGARIFNGALVGDRCEVRVNAIVHRRAVLPEGTVVPIGWVAVGDPVQLLSPDREAEIAAAQPELDFPGHVFGVDRDTPDLMVQLTERYGSSLARHAADRLL
>NZ_CP013859.1|WP_067202469.1|1890226_1893772_+|transcription-repair-coupling-factor
MRALEEASLYRDALTWAHTDADLGLVDGLDAPALAGLLRKRAENGHPAALLAVAPTGRRAESIAQALASYLPDAEVLTFPAWETLPHERLSPSPDTVGRRLQTLRRITGWTGDHPLVVVASVRAALQPIAGNLADIEPLELAIGSRGHELDDVAERLVERAYSRVDMVSRRGEFAVRGGILDVFPPTSEHPFRVEFFGDEIDQIRAFSVADQRSLPGDVSTVDLPPSRELLLTQEVRDNARALVGGFPAISAMLERMAEGIPVEGMESLLPAVAGPLKSLVEYLPDGAATAVVDPERSSARAITLGETNREFLDAAWSAATSGASAPIDLGAGDFLTIARLREIVHARGGVWWRLSPFAIGGADAETIDAAVIPSFHGNVDGAISFVDGCVSEGWRVVVIAAGPGLVDRARDVLSDRGVAARVVDRLTEAPEAGVATLVTGSVEAGVQVPEAKLAVLTDNEFYGRTIGGDQRVVKKLASRRKNVVDPLQLKQGDYVVHATHGIGRFVEMTQREVSTGGRNAAKSTRDYLVLEYAPSKRGYPGDKLFVPTDQLDLLSKYVGGEAPTLSKMGGSDWAQAKGRARKAVRDIAVELVKLYSARMSAKGHAFGPDTPWQRELEEAFPFAETHDQLQTIEEIKADMERPIPMDRLLSGDVGFGKTEVAVRAAFKAIQDGKQVAMLVPTTLLVKQHLETFTERFAGFPVKVRPLSRFQTDKEARLTLQGLLDGSVDMVIGTHRILTDQVIFKDLGLLIIDEEQRFGVEHKDALKKLKTNVDILAMSATPIPRTLEMAVTGIREMSTLQTPPEDRHPILSFVGPRSDKQIAAAIRREILREGQVFFVHNRVQSIQRVAAELAELVPEARIAVAHGKMGEHQLEQVVDDFWERKYDVLVSTTIIETGLDISNANTIIIDRADKYGLSQLHQLRGRVGRGRERAYAYFLYDDSKPLSETAADRLQTIAVNNDLGSGMQVALKDLELRGAGNLLGAEQAGHIAGVGFDLYLRMIGEAVATFRGEEVETGQELRLELPLEARIPEDYIDSERLRLEAYQKLSAASAATAKDDAIDLVVEELTDRYGTPPEEVVGLVAIARLRRRAARAGLTDVVAMGSNLRISPARLEDSIKVRMQRLYPKAKLVAGGEALVVPLPTVPSAVGVGLEPLPGAQLLEWVGQLFTALFPEPVKTD
>NZ_CP013859.1|WP_067198001.1|1889567_1890131_-|GNAT-family-N-acetyltransferase
MEPVTLITERLTLRAPTPSDAEAIERACQDPEIPRWTTVPSPYSRADAEDFIRLIAEWWADGSETVWSIFHEGVLVGSIGLHRIVDHHTGGHAELGYWVAAEARGHGFLAEAGKAVIDWGFAELGLVRIRWQAVVGNIPSARAARALGFRYEGLQRQALTGPRGRDDGWLGGLLVTDDRSPVEWPIL
>NZ_CP013859.1|WP_067197999.1|1888617_1889481_-|Fpg/Nei-family-DNA-glycosylase
MPEMPEVQGLTAFLDDRAVGRTITRAAVSAISALKTYDPPIHALQAAEVTGASRHGKFIVLSCGDDLHLVFHLAKAGWLRWYDELPTTLIKPGKSPIALRVALDDGAGFDLTEAGTKRSLAVYVVRDPHDVPGIARLGPDPLDPSFTRDVFAGLLEGKRMQIKGLLRDQGVIAGIGNAYSDEILHAARMSPYANAGKLDDAEIDRLYAAMQTTLAEAVAEASGKPPADLKDAKRRGMQVHARRGEACPVCGDTVRSVFFADRSMEYCPTCQTGGKPLADRRLSRLLK
>NZ_CP013859.1|WP_067197997.1|1887298_1888342_-|bifunctional-diaminohydroxyphosphoribosylaminopyrimidine-deaminase/5-amino-6-(5-phosphoribosylamino)uracil-reductase-RibD
MAVTEAERRAMTRALELAANGPRGVNPQVGAVILSSDGETMAEGWHRGAGTPHAEVDALSKLAPGAARGATAVVTLEPCNHTGRTGPCALALIDAGITRVVYALDDPGAVSGGGADRLRAAGVDVESGEQADAAHTLIDGWLTAQRLGRPHVTVKWAQSLDGRAAASDGSSQWITGPAARADVHRRRAESDAIVVGTGTVLADDPALTARDGDALLPHQPTPVVIGSRVTPADAALRRHPNSPLFYDTRDLHAVLADLHSRGVQRVFVEGGPTLASAFVASGLVDRVLAYVAPVLLGGDRLALTDLGIPSIDRALRLEIDEWVPLGPDLLAIAHPATATDSPTEGAD
>NZ_CP013859.1|WP_067197995.1|1886669_1887299_-|riboflavin-synthase
MFTGIIEEIGEITAIVPSGDGWRLTVRAPKAAADAVHGESIAVSGVCLTVVGSTADTFDTDVMKQTLDVAAIGSATVGTRVNIEKAMPVGARLGGHIVQGHVDGAGTVLEVRPGDQWSVLRISLPADLAPLVVDKGSIAVDGTSLTVSAVSPADAADAWFEVSLIPETLAATILGSRAVGDRVNLETDILARHVERLLAFRSAPEGGSR
>NZ_CP013859.1|WP_067197992.1|1885410_1886673_-|bifunctional-3,4-dihydroxy-2-butanone-4-phosphate-synthase/GTP-cyclohydrolase-II
MSLSTIPAALESLRAGRPVIVADDENRENEGDVILSAELATPEWVAWTVRWSSGFLCAPMPADLADALNLQPMVAANEDARSTAYTVSVDAAVGVTTGISAHDRARTLNVLADPSSTAHDLIRPGHVLPLRAVDGGVRERSGHTEAAVELMKLAGLRPVGAIAEVVAEDGSMMRMPGLLELGESAGVPVITIEQLIAHLNEIDPQGAVTTPGRRVSLRADATVPTSHGTFRFLAYKDRVSGTDHIAVVSGEPGDTALVRVHSECLTGEAFGSLKCECGPQLDAALDAIEKEGGVVIYMRGHEGRGIGLINKLRAYSLQEEGLDTVDANLALGLPADAREYAAAAGILTDLGISKVRLLTNNTDKVAQLRELGLDVIEQVPLIVGVGPNNHQYLETKRDRMGHIIGAEELAEALADGKEHE
>NZ_CP013859.1|WP_067197989.1|1884940_1885414_-|6,7-dimethyl-8-ribityllumazine-synthase
MSGAGAPKTGNIDARGLNVVIVAGTWHETITDGLIAGAQRVLDEASASHRLVRVPGSFELAVAAQAAFAGGADAVVALGVIIRGGTPHFDYVAAATTDGLTRVSLDAGKPVGFGVLTLDDEQQGLDRAGLPGSTEDKGAEAADAALRTALVTRELRG
>NZ_CP013859.1|WP_067197986.1|1884501_1884855_-|Fe-S-protein
METLRLVVVFVHLIGFAVLFGAWAAQAFGGTRKFTRVMDYGLAIAGLAGLALAAPWGISYDLNYVKIGVKLVVLLVIGAMLGIGSARQKRGEAVPAGVFWLVGVLTLANAGMGLLWR
>NZ_CP013859.1|WP_067197983.1|1883096_1884497_+|sugar-kinase
MSAPAAGFVVAIDNGSQSTKVLIVDAAGTVHASARVALRPYSSPAPGRWEHPGDDLWDSIVAATRAAVAGFGGDPREIRGIGLCTIRFCRAVLRADGTLAQPVMSWMDERLPRAYERESDDAVYVTTSSGYIGHRLTGQRTDAAGNVQGTWPIDTERWAWSRDAEDYARTGMDPSMLFDLVAPGEALGMLTAEAAAVLGLPAGIPVIATSNDKAVEALGAGLRDPEDALLSLGTYVATMTPGDRPVPPHPDVWTNFSSRPGGYLYESAGVRRGMWTVSWFRDLVSGGAEGVSEEGLNRGAESVPAGAGGLVAALDWLAPADEPWRRGALVGFDGTQGRFHVYRAILEALAIESEAGDERARRALGRARRRLVVTGGGSGSALMRQILAAVYGVPVRTPRVHDAAGMGAAICAAVGTGLHPTWDAAVDAMVAVGTEVAPEPHLVSAYAEVRQTYARVIPRIRLLFAD
>NZ_CP013859.1|WP_067198005.1|1895306_1896674_-|NADP-specific-glutamate-dehydrogenase
MTEPTADFHPLSTIAQPIFESVRALNPNEPEFHQAVHEVLHSIGPVLDRRPDYVDNGILERLVEPERQVIFRVPWIDDAGRLQVNRGYRVQYNSALGPYKGGLRFHPSVNISIIKFLGFEQIFKNALTGQGIGGGKGGSNFDPHGKSDAEIMRFCQSFMSELYRHIGEHTDVPAGDIGVGGREIGYMFGMYRKITNRHESGILTGKGIGWGGAQVRTEATGYGAVFFVQEMLAVHGESLEGKRVAVSGSGNVALYAIEKAQQLGAKAVTASDSSGYVVDDAGIDLALLRQIKEVERGRIVEYANRRPGARFVEGGNVWETPVDIAVPSATQNELNEDSALALIANGVRAVAEGANMPSTPEAVEAFQRAGVLFAPGKAANAGGVATSALEMSQNAARQRWDFANSEQKLRDIMADIHSAAFEAAERYGTPGDYVAGANIVGFERVADAMLAQGVI
>NZ_CP013859.1|WP_083511342.1|1896805_1899538_-|phosphoenolpyruvate-carboxylase
MSAGAVFRSRYPRRVTPAHSFPEPTNTEAIRVIGRFEAGRGIPEAMRSDVRMLGALLGQVLREAGSDGLFDDVERLRLATIQAYDEETPDAFERAAAIAESFSVSRADEVARAFTCYFHLVNLAEEHQRVRVLRERAGQPGREDAADTVASAYAKLKSEVGDDEARRRLEALRFHPVFTAHPTEARRRAVSSSIRRLSELLTQHDAASEGGAEQRRARRRMLEEIDTLWRTAPLRAQKPTPTDEVRTVMGVFDETLFTTVPHVYRRIDDALRGEESGSSAPVVPAFVRIGSWVGGDRDGNPFVTAAVTREASQIASDHVLRGLERAIERIGRTLTLDAEGTPPSEAVSALWEAFVAAEPDTAAELATRSPDEPHRRVMLALSRRVAATRRGGDLAYASPEELLADLRAVQSSLLAAGARRHAFGGVQHLIWQVETYGFHLTELEVRQHSQVHAKALAELDAGGPVSAQTEEVLEVFRVIAEIQRDRGLRAAGRYVVSFTQSAQDLAAVHRLARHAMGDDAPVLDVVPLFETFADLQAAPGILAEAVTFPEFQERLAATGNRLEVMLGYSDSSKDVGPVAANLALYEAQEKIAQWAKDSGIELTLFHGRGGALGRGGGPANSAILAQPPHSVDGRFKLTEQGEVIFARYGEPAIAMRHIDQVAAATLLASSPSVEERTSSAATRYAEVARTMDVASRERFFSLVKAEGFAPWFATVTPMEEIGLLALGSRPARRGLSVESLEDLRAIPWVFAWTQARINLAGWFGLGTALEAVGDEDLLVEAYREWPLLHTMIDNVAMSLAKTDERIARQYLALGDRDDLAALVLDELALTRRWVIRLTGGDRLLENKPVLQRAVQLRSPYVDALSLLQLRALRALRASAGQAEGSGADAEQQRLLLLSVSGVAAGLQNTG
>NZ_CP013859.1|WP_067198009.1|1899590_1900757_+|Na+/H+-antiporter-NhaA
MRISANPLRGQQFPAVLLLLAAGLGLLLANLMTHDAIEGVLELHLAVPGTALDLSVGHWISDGLLAVFFLVVAIELRHELTHGELDSPRKAVQPAIAAAGGVLVPIAVYLLLAGDFTTVAGWPVPTATDIAFALGVLAMFGRGLPPTVRVFLLALAILDDIIGIVFIAVLFAHDVQWLLLALAVVCVIAFWALSRLLHATGHTLVAVAMAVVGVVTWGLVAASGIHATIAGVLLGLVMAPVPAGRVRHALEPAVNGVILPLFAFVAAFVVIPAVSPTELSPAFWGILVALPVGKIIGISLFGWVAMRIRPKGAPPALPFADLVAAGALGGIGFTVSLLLANLAFAGDAGIRDQAILGVLLGSLVALVLSGVIVSLRAGWYRRVAAAAE
>NZ_CP013859.1|WP_067198012.1|1900770_1901520_+|MazG-family-protein
MTDTPEDDPLRAVAETMRAVRERCVWSQRITHRDLVPYLIEEAHEVIDAVEAGSRDDLREELGDLLWQVLFHSAIAAQDEDDPFDIDDVARGLNEKMVRRHPHVFGGAVARTPEEVLVHWNAAKAAEKRTRRSALDGIPRGMPALALAQKMLGRVPPAPLPATADAATTDAATTGTDGGRPSSEAELGEALLSLVRAARENGWDAERALRERLRALEAEVRAAEERAGEGLSAEGRGGRRSAEERAGEG
>NZ_CP013859.1|WP_083511183.1|1901554_1902823_+|histidine--tRNA-ligase
MNPPRGMRDILPADKARREHVLSIIRDRYRSHGFDEIETPALEEYSRLHAGIGGDNEKLAYNVLRRGLDAEAIREAADDPAALADLGLRYDLTVPLARFYASNRGQLPGVFRSIQIGPVWRAERPQKGRYRQFVQCDIDIMGDDSARAEAELMVASLDALDALGLEGATVRVNDRRVLDWMLESFGFALDERPGVLITIDKLDKIGPDGVAAELRERGADSGAVGAFEAFLRRPQTMEYNPFGERQIRKALPDGAPDEIVAHLVGIGDAVAAGTGRSDVPLVFDPFLVRGMGYYTGTIFELAHPSVDYSLGGGGRYDGMIGRFLGQQVPAVGFSLGFERLVDLVRTETDAVARAVVLIHDADVPVAELVAHKSRLIAGGARVRLEKRTKNLKALLERSAAGGYTAFATVPSGAQELELKPLS
>NZ_CP013859.1|WP_067202472.1|1902891_1903686_+|SGNH/GDSL-hydrolase-family-protein
MAVAGLGLAACAVGVRVLLARQAAIARRRIGKPLGEESIDADRVWRRSLGGEPVELLLLGDSLAAGLGAERRKQTLGARLAKDLAARVRRPVRLRTAAVVGAESPDLGGQLDSLPDDYRPDVAVIVVGGNDVTHRIPASVSAAHLGDAITRLRVKGTQVVVGTCPDLGALRAVPQPLRRLAASISRRLAAVQAETAAGAGADAVDLRRAVGAMFSDDPDQMFSLDRFHPSALGYRRTAEALLPAVHRAVERGVRSGDPVTPPAR
>NZ_CP013859.1|WP_067198017.1|1903666_1904179_-|glyoxalase
MTNHTSAGASGQHTTDGRPHNATSLTPFLAIPRAKEAIEFYRDVFDARVVDVTEFGGVVAHADLDFGLGLLQRGEPHPDYHLVAPPDGDDDCYSMGLYVPDVDAVVERAVDAGATVREAPSDFVSGDRFASIRDPFGVRWSIMTRIEDISEEESARRVSEWAASFSAPAE
>NZ_CP013859.1|WP_067198019.1|1904253_1905036_+|AraC-family-transcriptional-regulator
MVDPTRGVLYPGRLPQFHRLPAEGEAADLVAWVWIPEWDLAPGETSRQDIVGYPALNLVVERDAVTLAGATTRVSHRDLRGRGWAVGALLRPAAVPALTPAPAAIIDEEVRLHEPVLRRAVADAMESGGEGYRRRAALALAEWLVARVGPLDAHGRQANAMTDVLLGPGAAGSPEEAATRLAVSVRTLQRLAHRHVGMSPGAMIRRRRLHDAAERLRGDPAVDLAALAAESGYADHAHLTRDFRAVLGITPRAYRARASG
>NZ_CP013859.1|WP_067198022.1|1905036_1906272_-|APC-family-permease
MPLVRRLGLRDAVAIGLGSMIGAGVFSVWGPALGAAGSGLLAALAIAAAVAYCNATASAQLAAVHPVAGGTYAYARAEIGPWWGFVAGWCFVVGKIASCAAMAMTFAAYAAPPGWERPVAVLAVAALGAVNCIGITRTAGLTRLLVAVSLTGLAVVVAVGFSSAPSAAPSALPDSTAYGVLQAAGLLFFAFAGYARIATMGEEVSDPARTIPRAIVLALAVVVAVYALVAVVVLLTLGIDAAATRAPLAEVLTRAGWPALAPVVRVAAAAASLGALLALLTGIGRTTLAMAREADLPTFFARIDDRFHVPRRAEIAITLVVIGIVAAADLRGAIGFSSFGVLLYYLIANAAAFRQSGPARRYPRALQVVGALGCLLLVTTLPVVASAVGLGVVLLGVGYRMLRLRVRRGRA
>NZ_CP013859.1|WP_067198024.1|1906336_1906807_-|DUF4442-domain-containing-protein
MRITPRRLAIGMSLWIPNLFSGIRVRRFSDDWTHATVELHVNLFTRNYVKTAFGGSMSAMTDPYFFMLVMHQLGRDYVVWDTRGEIEFVKPGRGVLTAEFEVTRERAEQIRARAEGGAKVLEWFETVITDREGDVVARVRREVYVREKRRVTAARA

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_CP013859_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP013859_7

2361559-2361666

Orphan

Consensus_repeat	Method
CCGCCCTCTCCCGCGCCGAGGAGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP013859_7

>merge|NZ_CP013859|7|2361559-2361666|CRISPRCasFinder
CCGCCCTCTCCCGCGCCGAGGAGAAGCGGGACGAGTTGGAGGCGAATCTGATACTCGCAGGGGCAACAGTCTCCGACGTGCTTTCCGCCCTCTCCCGCGCCGAGGAGA

>NZ_CP013859|7|7|2361559-2361666|CRISPRCasFinder
CCGCCCTCTCCCGCGCCGAGGAGA	AGCGGGACGAGTTGGAGGCGAATCTGATACTCGCAGGGGCAACAGTCTCCGACGTGCTTT
CCGCCCTCTCCCGCGCCGAGGAGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP013859.1\|WP_067198876.1\|2357677_2358061_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198905.1\|2364018_2364486_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198889.1\|2360860_2361178_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198873.1\|2356465_2357656_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273206
NZ_CP013859.1\|WP_067198897.1\|2362728_2362971_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067202622.1\|2364655_2364898_+\|TM2-domain-containing-protein	unknown	unknown	gnl\|CDD\|377473
NZ_CP013859.1\|WP_067198885.1\|2358911_2359952_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198899.1\|2362967_2363417_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198901.1\|2363409_2363634_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198907.1\|2364915_2365209_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_157541031.1\|2355731_2356469_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379352
NZ_CP013859.1\|WP_067198882.1\|2358735_2358915_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_083511214.1\|2359948_2360218_+\|WhiB-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376791
NZ_CP013859.1\|WP_157541034.1\|2362526_2362736_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198903.1\|2363626_2363869_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198887.1\|2360214_2360868_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198878.1\|2358050_2358536_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198893.1\|2361777_2362527_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198909.1\|2365671_2366037_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP013859.1\|WP_067198880.1\|2358532_2358736_+\|hypothetical-protein	unknown	unknown	unknown

>NZ_CP013859.1|WP_067198889.1|2360860_2361178_+|hypothetical-protein
MTDFAALWKATAKKLASDIRELEAINSALRQAVRFHARKRDEASHAAGRHKSDAALYEAALSRAEETIERIDGEVKDFEQSDNDAIVAIEEILIDYDKQKGDRSE
>NZ_CP013859.1|WP_067198887.1|2360214_2360868_+|hypothetical-protein
MITDTDIFQAELRRWVERYEQHLDQLPVLLEHLRDRANPMKAGSLEERVGGGGGDTPAPFRLDPVDDCDDLWSSLVEYIGEVAERLQDPAPGAAGASWAVKGSVRGIPAWMGPDEAYRAAYELIAWLIDRAEKVHALALKDSEDHLFSLIRKLMTRYVIPPIERPSHRRLCIGEDEEGRMVGCGERAVVVDWIIGDVGEARCAVCGAVYTREEDTHD
>NZ_CP013859.1|WP_083511214.1|2359948_2360218_+|WhiB-family-transcriptional-regulator
MTDTMRVFTEVLVTPAPWMRDALCAQSDPDLWFPPKGGEGGAEAKRICQSCDVIGQCLAYALEHNETVGIWGGKSPKERQRIRREGRAA
>NZ_CP013859.1|WP_067198885.1|2358911_2359952_+|hypothetical-protein
MTGKPQTCTHRGCSRKPVARRLCHAHYQAAWKAGELTAHAKLPPRPKKHDHVCPDDHKHASASTCFIQHQCRCEPCVEAHNARERNRKKQKAYGRFDTGLVDVAPVREHVLKLGEFGIGYKRVAQLAGFKSSTPVRTIVWGRQDPGPRFGEMQKRVKRETAEKILAIQPVIDNLAPGQKIAASGTHRRLQALVVAGWSMSKLANLLGLDPSNFSTFMQRDTVLVSTWIAVRDLFDELWDQEPPHAEWRDKIAFSRSQRYAKLHGWLPALAWDDIDTDPEPPTVEVDEQTKGERILEDVEWLLEAGEPVEQVAMTLGRSMDAIAKLAQRHHRLDLARPFWAKVRRAA
>NZ_CP013859.1|WP_067198882.1|2358735_2358915_+|hypothetical-protein
MPLSYPPIRAVEVDGEKRWQATCRTCGQDVCSRPQVVKAAVDEMRRAHGYEAECRRAER
>NZ_CP013859.1|WP_067198880.1|2358532_2358736_+|hypothetical-protein
MSEGPIKQWRDGHKTDRVSTPDAHRVCAPSPVKGRGYCGRKNDRTAPFKDATCSDCHAAARADKEAG
>NZ_CP013859.1|WP_067198878.1|2358050_2358536_+|hypothetical-protein
MSSDALCPACTKTAEALGHTAEERLAALGWSPTGFQMQSYHDGVWTPMENGNASKHWAPKKSRYEAVHMCIAWTGGVCIPAMRVVDLSTGKVIWQDRWDGGNAADLDQIIPEWARAIYGQVRAEQRESQAVLDHAVDEYVPDRKTAPADDCALFSLAEMDS
>NZ_CP013859.1|WP_067198876.1|2357677_2358061_+|hypothetical-protein
MAKLILENVIVDRVFSTQHGYGVGVTETFEMRNGETGRKRYTLWFNDHPGVEEGQRISASGFLGTKVREYESNGETRTAVDVSVYSARLIQSAPPIDPAPETDSWTPQATGDAWSTPQSSDTWGGEF
>NZ_CP013859.1|WP_067198873.1|2356465_2357656_+|AAA-family-ATPase
MSIVDAERAVIGAIIKDSSVLRKVQAEVMPSDFYDGRLGDIYRGITHMSTTREPIDYLTVYGHLAEWGVVGVELPQLAAWVDAVPTASNADFYAAQVRQASLARGLKVIAARVQEAADTMPPEQLISRTADELRDLREHHTIEDVHAMALDEVLTQEVEYDWVIPDLLERRDRFMITGIEGGGKSTLIRQLAITAAAGIHPFREYPIDPVRVLVVDAENTEKQWGRETRRWAPSMNMLDGQDMYKRLHLACMRRLDLTKDIDLGMVHRLVDQYSPDMLFIGPMYRLAPKLNNDEDAAPLLGALDTLRDRGLALVIEAHAGHQTNPQGERDLRPRGSSQLMGWPEFGYGLRRSKKNPLHVDMVRWRGDRDARGWPAKLGRAAPGVTGTQRWPWRPVD
>NZ_CP013859.1|WP_157541031.1|2355731_2356469_+|hypothetical-protein
MSVKVSSWVWHGEETAELAGNEMILLLALADVADDNGRCRFLTEDDDLSYRGLARKARVSRSTVIRIMAKFRDANLIEQVKGVKGRSNEIRIIVPWARQSGSKLEPIAPDGPNDSVPSETDSVPTEQEFGSKSDEHASLIRKDVIDVARVRPGFAEFYLIYPRKVGKEAARKAFEKAAKSTEPEVIIEGARRFAADPNLPEKQFIPHPATWLNAGRWDDEPLPPRVGAEHPEVPDYGRDEWMYRA
>NZ_CP013859.1|WP_067198893.1|2361777_2362527_+|hypothetical-protein
MADRFQGESDPIATNPILRGVDLAVDRLVRADCFTERTLRVLDELRAEVLAAEQAHTQTDDERVSLMDAATDAFAKHEGAPTWQDDPVGRDAALRWHMRGFEDGLNARRAVHTPTDDEREVLRRVREFATKERDSIRGRYGADSATYAGYANACDDILSILDGDPSAHGRDRDGICRRCGHALTAAEVLDGETPCEPQGEPSDAAVIAGAEAMCEQGPANTPIWDDWVWERFSRAALRAAAEVRGERWA
>NZ_CP013859.1|WP_157541034.1|2362526_2362736_+|hypothetical-protein
MFYDRQVNYKVAYVRIDNENSVAELADALSEFGIEDATWTVEPSYIVLSREMSTTEVPAVVGQGGENRG
>NZ_CP013859.1|WP_067198897.1|2362728_2362971_+|hypothetical-protein
MAESPSINIQIDEQALRDQIDKTVQDAFREASMRLRLAADALDGGEWIRGFEEHQEQRLRDEYERGRKHALAEQEGQVDR
>NZ_CP013859.1|WP_067198899.1|2362967_2363417_+|hypothetical-protein
MSEYTPTMQELKDYATSYTAMASEAEWDRALAAHDAEVRAAQHIVSCARCGAKPVVASDALNSDIVVCGDCGVQIGLHELQEVRAGVVAEEPEGEHVFIERYGMYHAKFGGIGGDVSSLTLTREAWKALGEADVLAVSVVPVEQGDGDA
>NZ_CP013859.1|WP_067198901.1|2363409_2363634_+|hypothetical-protein
MPEPIAASIRAELDQTPEWWQQQYDALVRKQIPRTPEHHAGHDLAEPIRSWGGATLTRPWCTSCGVPIERAPDG
>NZ_CP013859.1|WP_067198903.1|2363626_2363869_+|hypothetical-protein
MAEYLTYREAATRVRRSIRSINRWRRQGMPMGWEVRDGQRVRVVDETILLAWWRDRLTAWPPHQYRLRRMLTDDDTRHAE
>NZ_CP013859.1|WP_067198905.1|2364018_2364486_-|hypothetical-protein
MDSQAELALNVVLAITSAVGAGIAIWQAVVAKGARDDAEVHARRALEIAERQSAAQEAIAARLKPAPWSDLINVSGQLYATKNTSGEALTITNVSVTPDSAFPMFKPRTPIPSTLQPGDAFRAMLVGRYGLAIDTVVVEWTAASGETGTTRLAKP
>NZ_CP013859.1|WP_067202622.1|2364655_2364898_+|TM2-domain-containing-protein
MKDTGIAYLLAILLGGFAAHRFYLGQIGSAVAFLVLWWGGWALTFIFIGFVMVAIAAVWWIVDLFIIPSMVRTANGMRSQ
>NZ_CP013859.1|WP_067198907.1|2364915_2365209_+|hypothetical-protein
MGDLHHGRGYKAYRRKRAALKRRVERENLPCGYGGNYGCGEPFDLSIPYPDPMSFSADHPEALGNGGHMVKQDLVPMHLGCNSRKGDAAEVEIWEAS
>NZ_CP013859.1|WP_067198909.1|2365671_2366037_+|hypothetical-protein
MAAMKADSAARRASADDDAQSAPIVALPGGSVAMPAAPQGDVDARAELLANMALVKRAMEAIAEADPLKIVQLSKRHSELVDELVKVSGTAPAGPAAEEADPFAFLGDASRRPAPAPRKSS

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_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NZ_CP013859.1	1318180-1318206	2	0.926

1. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to position: 1318180-1318206, mismatch: 2, identity: 0.926

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
cccgcagccgcctgccgcaccgcagcc	Protospacer
******************..*******

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	MN369741	Mycobacterium phage LoneWolf, complete genome	27725-27751	3	0.889
NZ_CP013859_5	5.2\|1317985\|27\|NZ_CP013859\|CRISPRCasFinder	1317985-1318011	27	NC_009444	Pseudomonas fluorescens SBW25 plasmid pQBR103, complete sequence	37396-37422	4	0.852
NZ_CP013859_5	5.3\|1318039\|24\|NZ_CP013859\|CRISPRCasFinder	1318039-1318062	24	KU984979	Propionibacterium phage PFR1, complete genome	14158-14181	4	0.833
NZ_CP013859_5	5.3\|1318039\|24\|NZ_CP013859\|CRISPRCasFinder	1318039-1318062	24	NC_031108	Propionibacterium phage PFR2, complete genome	15727-15750	4	0.833
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_LR134461	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 19, complete sequence	109350-109376	4	0.852
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NC_013449	Streptomyces sp. W9 plasmid pCQ3, complete sequence	40563-40589	4	0.852
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NC_019307	Streptomyces sp. W75 plasmid pCQ4, complete sequence	45276-45302	4	0.852
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_CP034352	Streptomyces sp. W1SF4 plasmid p2, complete sequence	23018-23044	5	0.815
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	232125-232151	5	0.815
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_AP017658	Sphingobium cloacae strain JCM 10874 plasmid pSCLO_4, complete sequence	9307-9333	5	0.815
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_AP017659	Sphingobium cloacae strain JCM 10874 plasmid pSCLO_5, complete sequence	24086-24112	5	0.815
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_AP017661	Sphingobium cloacae strain JCM 10874 plasmid pSCLO_7, complete sequence	17378-17404	5	0.815
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_CP013918	Sphingomonas sp. LK11 plasmid unnamed1, complete sequence	11800-11826	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NC_014718	Paraburkholderia rhizoxinica HKI 454 plasmid pBRH01, complete sequence	299113-299139	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MK814757	Gordonia phage Fairfaxidum, complete genome	45752-45778	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NZ_CP025017	Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence	160271-160297	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NZ_CP028350	Pantoea vagans strain PV989 plasmid pPV989-508, complete sequence	402695-402721	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NC_014258	Pantoea vagans C9-1 plasmid pPag3, complete sequence	169243-169269	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MH536817	Mycobacterium phage Druantia, complete genome	28606-28632	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	JX307703	Mycobacterium phage Sabertooth, complete genome	28602-28628	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KF024733	Mycobacterium phage Medusa, complete genome	28602-28628	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KY204245	Mycobacterium phage Camperdownii, complete genome	28276-28302	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KY083058	Mycobacterium phage Abdiel, complete genome	28604-28630	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MT889390	Mycobacterium phage Bartimeaus, complete genome	28605-28631	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MK359323	Mycobacterium phage Baby16, complete genome	28614-28640	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KX557234	Mycobacterium phage Florean, complete genome	28602-28628	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MG099942	Mycobacterium phage Blackmoor, complete genome	28605-28631	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MT889386	Mycobacterium phage CentreCat, complete genome	28606-28632	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KX619651	Mycobacterium phage Roosevelt, complete genome	28605-28631	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KF841476	Mycobacterium phage Melvin, complete genome	28601-28627	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MK359325	Mycobacterium phage Eros, complete genome	28605-28631	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KX579975	Mycobacterium phage Mundrea, complete genome	28363-28389	5	0.815
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	1958696-1958722	6	0.778
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MF377441	Arthrobacter phage Timinator, complete genome	13858-13884	6	0.778
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MT310895	Arthrobacter phage StevieBAY, complete genome	13858-13884	6	0.778
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	KU647629	Arthrobacter phage BarretLemon, complete genome	13859-13885	6	0.778
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	MH825703	Arthrobacter phage LeeroyJ, complete genome	13858-13884	6	0.778
NZ_CP013859_5	5.2\|1317985\|27\|NZ_CP013859\|CRISPRCasFinder	1317985-1318011	27	NC_015162	Deinococcus proteolyticus MRP plasmid pDEIPR02, complete sequence	146784-146810	7	0.741
NZ_CP013859_5	5.4\|1318090\|27\|NZ_CP013859\|CRISPRCasFinder	1318090-1318116	27	NZ_CP054618	Azospirillum oryzae strain KACC 14407 plasmid unnamed4, complete sequence	26614-26640	7	0.741
NZ_CP013859_5	5.5\|1318144\|27\|NZ_CP013859\|CRISPRCasFinder	1318144-1318170	27	NZ_CP025013	Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence	693703-693729	7	0.741

1. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to MN369741 (Mycobacterium phage LoneWolf, complete genome) position: , mismatch: 3, identity: 0.889

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cccaccgcagccggcggctccgcagcc	Protospacer
* ********** *****.********

2. spacer 5.2|1317985|27|NZ_CP013859|CRISPRCasFinder matches to NC_009444 (Pseudomonas fluorescens SBW25 plasmid pQBR103, complete sequence) position: , mismatch: 4, identity: 0.852

ctcgctgaccgctgcgtacccgcctgc	CRISPR spacer
ctcgctgaccgctgcgaagccgccgga	Protospacer
**************** * ***** *

3. spacer 5.3|1318039|24|NZ_CP013859|CRISPRCasFinder matches to KU984979 (Propionibacterium phage PFR1, complete genome) position: , mismatch: 4, identity: 0.833

tcactcgcggcttgttgagccgca	CRISPR spacer
ggactcgcggctggttgagccgcg	Protospacer
  ********** **********.

4. spacer 5.3|1318039|24|NZ_CP013859|CRISPRCasFinder matches to NC_031108 (Propionibacterium phage PFR2, complete genome) position: , mismatch: 4, identity: 0.833

tcactcgcggcttgttgagccgca	CRISPR spacer
ggactcgcggctggttgagccgcg	Protospacer
  ********** **********.

5. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_LR134461 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 19, complete sequence) position: , mismatch: 4, identity: 0.852

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
ggtcccgcagcccgcggccccgcagcc	Protospacer
 *. ********.**************

6. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NC_013449 (Streptomyces sp. W9 plasmid pCQ3, complete sequence) position: , mismatch: 4, identity: 0.852

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gccgcagccgcctgccgagtcgccggc	Protospacer
 **************** ***** * *

7. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NC_019307 (Streptomyces sp. W75 plasmid pCQ4, complete sequence) position: , mismatch: 4, identity: 0.852

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gccgcagccgcctgccgagtcgccggc	Protospacer
 **************** ***** * *

8. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP034352 (Streptomyces sp. W1SF4 plasmid p2, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cgcaccgccgcctgcggctccgcactg	Protospacer
******** *********.***** .

9. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
ggtcccgcagccgtcggccccgcagcc	Protospacer
 *. ********  *************

10. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_AP017658 (Sphingobium cloacae strain JCM 10874 plasmid pSCLO_4, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cgcgccgcagcctgccgccccgcgccg	Protospacer
***.*********** *******. *

11. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_AP017659 (Sphingobium cloacae strain JCM 10874 plasmid pSCLO_5, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cgcgccgcagcctgccgccccgcgccg	Protospacer
***.*********** *******. *

12. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_AP017661 (Sphingobium cloacae strain JCM 10874 plasmid pSCLO_7, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cgcgccgcagcctgccgccccgcgccg	Protospacer
***.*********** *******. *

13. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP013918 (Sphingomonas sp. LK11 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
cgcgccgcagcctgccgccccgcgccg	Protospacer
***.*********** *******. *

14. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NC_014718 (Paraburkholderia rhizoxinica HKI 454 plasmid pBRH01, complete sequence) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
accgcagcggcctgccgcgccgcagta	Protospacer
 ******* **********.*****.

15. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MK814757 (Gordonia phage Fairfaxidum, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gccgcagccgccgcccgcgtcgcagag	Protospacer
 ***********  ***********

16. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP025017 (Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
accgcagccgccggccgcatcgcacct	Protospacer
 *********** *****.***** *.

17. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP028350 (Pantoea vagans strain PV989 plasmid pPV989-508, complete sequence) position: , mismatch: 5, identity: 0.815

cccgcagc--cgcctgccgcgtcgcagcc	CRISPR spacer
--ggtaacagcgcctgccgcgtcgcagcc	Protospacer
   *.*.*  *******************

18. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NC_014258 (Pantoea vagans C9-1 plasmid pPag3, complete sequence) position: , mismatch: 5, identity: 0.815

cccgcagc--cgcctgccgcgtcgcagcc	CRISPR spacer
--ggtaacagcgcctgccgcgtcgcagcc	Protospacer
   *.*.*  *******************

19. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MH536817 (Mycobacterium phage Druantia, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

20. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to JX307703 (Mycobacterium phage Sabertooth, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

21. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KF024733 (Mycobacterium phage Medusa, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

22. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KY204245 (Mycobacterium phage Camperdownii, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

23. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KY083058 (Mycobacterium phage Abdiel, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

24. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MT889390 (Mycobacterium phage Bartimeaus, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

25. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MK359323 (Mycobacterium phage Baby16, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

26. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KX557234 (Mycobacterium phage Florean, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

27. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MG099942 (Mycobacterium phage Blackmoor, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

28. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MT889386 (Mycobacterium phage CentreCat, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

29. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KX619651 (Mycobacterium phage Roosevelt, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

30. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KF841476 (Mycobacterium phage Melvin, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

31. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MK359325 (Mycobacterium phage Eros, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

32. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KX579975 (Mycobacterium phage Mundrea, complete genome) position: , mismatch: 5, identity: 0.815

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
tgcacagcggcctgccgcgttgcagcc	Protospacer
. *.**** ***********.******

33. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
cagttcgccgcctggcgcgtcgcagcc	Protospacer
*   . ******** ************

34. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MF377441 (Arthrobacter phage Timinator, complete genome) position: , mismatch: 6, identity: 0.778

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gtcgcagacgcctgccgcgacgcagag	Protospacer
 .***** *********** *****

35. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MT310895 (Arthrobacter phage StevieBAY, complete genome) position: , mismatch: 6, identity: 0.778

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gtcgcagacgcctgccgcgacgcagag	Protospacer
 .***** *********** *****

36. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to KU647629 (Arthrobacter phage BarretLemon, complete genome) position: , mismatch: 6, identity: 0.778

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gtcgcagacgcctgccgcgacgcagag	Protospacer
 .***** *********** *****

37. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to MH825703 (Arthrobacter phage LeeroyJ, complete genome) position: , mismatch: 6, identity: 0.778

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
gtcgcagacgcctgccgcgacgcagag	Protospacer
 .***** *********** *****

38. spacer 5.2|1317985|27|NZ_CP013859|CRISPRCasFinder matches to NC_015162 (Deinococcus proteolyticus MRP plasmid pDEIPR02, complete sequence) position: , mismatch: 7, identity: 0.741

ctcgctgaccgctgcgtacccgcctgc	CRISPR spacer
tggagggacagctgcgtacccgcctgc	Protospacer
.  .  *** *****************

39. spacer 5.4|1318090|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP054618 (Azospirillum oryzae strain KACC 14407 plasmid unnamed4, complete sequence) position: , mismatch: 7, identity: 0.741

cgcaccgcagcctgcggccccgcagcc	CRISPR spacer
tgttccgcagcctgcggccccgccatg	Protospacer
.*. ******************* ..

40. spacer 5.5|1318144|27|NZ_CP013859|CRISPRCasFinder matches to NZ_CP025013 (Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence) position: , mismatch: 7, identity: 0.741

cccgcagccgcctgccgcgtcgcagcc	CRISPR spacer
agcgcagccgcccgccgcgtcgctata	Protospacer
  **********.********** ..

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

2349905 : 2360218

Gordonia_phage(25.0%)

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_067198846.1\|2349905_2350181_+	helix-turn-helix transcriptional regulator	A0A1W6JRC7	Corynebacterium_phage	7.3e-12	60.3
WP_157541021.1\|2350195_2350387_+	hypothetical protein	NA	NA	NA	NA
WP_157541024.1\|2350383_2350650_+	hypothetical protein	NA	NA	NA	NA
WP_157541028.1\|2350677_2351211_+	hypothetical protein	NA	NA	NA	NA
WP_083511213.1\|2351200_2351926_+	hypothetical protein	G8I8E1	Mycobacterium_virus	4.8e-10	30.9
WP_067198857.1\|2351925_2352186_+	hypothetical protein	NA	NA	NA	NA
WP_067198859.1\|2352182_2353328_+	hypothetical protein	NA	NA	NA	NA
WP_083511356.1\|2353168_2354251_+	recombinase RecT	A0A1B3AZ87	Gordonia_phage	1.4e-37	46.6
WP_067198864.1\|2354247_2354592_+	hypothetical protein	NA	NA	NA	NA
WP_067198866.1\|2354588_2355068_+	hypothetical protein	NA	NA	NA	NA
WP_067198868.1\|2355064_2355331_+	hypothetical protein	NA	NA	NA	NA
WP_067198869.1\|2355327_2355732_+	hypothetical protein	A0A0U4IKC7	Arthrobacter_phage	3.8e-17	46.4
WP_157541031.1\|2355731_2356469_+	hypothetical protein	A0A2K9VGL5	Pontimonas_phage	2.2e-18	53.2
WP_067198873.1\|2356465_2357656_+	AAA family ATPase	A0A1P8VV42	Rathayibacter_phage	5.2e-70	39.5
WP_067198876.1\|2357677_2358061_+	hypothetical protein	NA	NA	NA	NA
WP_067198878.1\|2358050_2358536_+	hypothetical protein	NA	NA	NA	NA
WP_067198880.1\|2358532_2358736_+	hypothetical protein	NA	NA	NA	NA
WP_067198882.1\|2358735_2358915_+	hypothetical protein	NA	NA	NA	NA
WP_067198885.1\|2358911_2359952_+	hypothetical protein	A0A142K8V3	Gordonia_phage	2.4e-23	33.3
WP_083511214.1\|2359948_2360218_+	WhiB family transcriptional regulator	A0A2P1CGA4	Mycobacterium_phage	1.8e-15	58.3

DBSCAN-SWA_2

2366065 : 2376037

Rathayibacter_phage(42.86%)

portal,capsid

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_067198911.1\|2366065_2367484_+	hypothetical protein	A0A1P8VV92	Rathayibacter_phage	2.7e-126	53.2
WP_067198913.1\|2367480_2368941_+\|portal	phage portal protein	A0A2D1GPM7	Mycobacterium_phage	4.0e-24	27.2
WP_067198915.1\|2368949_2369594_+	hypothetical protein	A0A0K1LT09	Mycobacterium_phage	8.3e-06	41.1
WP_067198917.1\|2369662_2370604_+\|capsid	phage major capsid protein	A0A0C5ADQ6	Mycobacterium_phage	2.9e-76	53.2
WP_067198918.1\|2370622_2370958_+	hypothetical protein	NA	NA	NA	NA
WP_157541039.1\|2370884_2371301_+	hypothetical protein	NA	NA	NA	NA
WP_067198922.1\|2371300_2371693_+	hypothetical protein	NA	NA	NA	NA
WP_067198925.1\|2371697_2371967_+	hypothetical protein	A0A1P8VV83	Rathayibacter_phage	9.0e-07	39.0
WP_067198927.1\|2371963_2372389_+	hypothetical protein	NA	NA	NA	NA
WP_067198929.1\|2372459_2373029_+	hypothetical protein	A0A1P8VV84	Rathayibacter_phage	2.3e-23	40.3
WP_067198931.1\|2373127_2373526_+	hypothetical protein	NA	NA	NA	NA
WP_157541041.1\|2373871_2376037_+	hypothetical protein	A0A2K9VH55	Gordonia_phage	1.4e-20	35.1

DBSCAN-SWA_3

3191344 : 3205954

Streptomyces_phage(45.45%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_067201077.1\|3191344_3192307_+	hypothetical protein	A0A2H5BLD0	Streptomyces_phage	1.8e-36	36.1
WP_067201078.1\|3192381_3192861_+	hypothetical protein	NA	NA	NA	NA
WP_067201080.1\|3192860_3193217_+	hypothetical protein	NA	NA	NA	NA
WP_067201086.1\|3193213_3193501_+	hypothetical protein	A0A142K9Z8	Gordonia_phage	8.2e-06	38.4
WP_067201089.1\|3193497_3193911_+	hypothetical protein	NA	NA	NA	NA
WP_067201096.1\|3193917_3194481_+	hypothetical protein	Q6VY45	Streptomyces_phage	3.2e-38	45.3
WP_067201101.1\|3194585_3194864_+	hypothetical protein	NA	NA	NA	NA
WP_067201106.1\|3194983_3195202_+	hypothetical protein	NA	NA	NA	NA
WP_067201122.1\|3195211_3197560_+	hypothetical protein	A0A2R4A056	Microbacterium_phage	6.9e-50	44.3
WP_067201124.1\|3197567_3198446_+	hypothetical protein	A0A2R4A2E6	Microbacterium_phage	1.1e-21	32.8
WP_083511273.1\|3198409_3200290_+	hypothetical protein	A0A291LHU4	Streptomyces_phage	1.0e-64	39.5
WP_157541136.1\|3200295_3200442_+	hypothetical protein	NA	NA	NA	NA
WP_067201129.1\|3200519_3201425_+	hypothetical protein	A0A0K1Y8X4	Streptomyces_phage	4.0e-30	40.4
WP_067201131.1\|3201421_3202237_+	hypothetical protein	A0A2R4A190	Microbacterium_phage	1.7e-16	35.6
WP_067201134.1\|3202303_3203086_+	peptidoglycan-binding protein	A0A2L0HNW5	Microbacterium_phage	5.0e-82	62.4
WP_067201137.1\|3203085_3203316_+	hypothetical protein	NA	NA	NA	NA
WP_067201139.1\|3203325_3203604_+	hypothetical protein	NA	NA	NA	NA
WP_157541139.1\|3203764_3203920_+	hypothetical protein	NA	NA	NA	NA
WP_067201142.1\|3203991_3204249_+	hypothetical protein	NA	NA	NA	NA
WP_067201145.1\|3204310_3204679_+	hypothetical protein	NA	NA	NA	NA
WP_067201148.1\|3204675_3205269_+	hypothetical protein	A0A2L1IYZ3	Streptomyces_phage	1.2e-30	45.9
WP_157541142.1\|3205357_3205954_+	hypothetical protein	O21963	Arthrobacter_phage	4.3e-09	37.5

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_CP013859

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

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection