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_CP009280	Paenibacillus sp. FSL P4-0081, complete genome	20 crisprs	cas3,PrimPol,WYL,csa3,cas14j,RT,DEDDh,DinG	3	4	9	0

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP009280_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_1

1232926-1233018

Orphan

Consensus_repeat	Method
TATGCTTTCGAAGCCAGTTTTGTCAGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_1

>merge|NZ_CP009280|1|1232926-1233018|CRISPRCasFinder
TATGCTTTCGAAGCCAGTTTTGTCAGCAACTCATTCGCCTGAGCTGCTGCATCAAAACTTGGAGATTATGCTTTCGAAGCCAGTTTTGTCAGC

>NZ_CP009280|1|1|1232926-1233018|CRISPRCasFinder
TATGCTTTCGAAGCCAGTTTTGTCAGC	AACTCATTCGCCTGAGCTGCTGCATCAAAACTTGGAGAT
TATGCTTTCGAAGCCAGTTTTGTCAGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_156118531.1\|1222239_1222392_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_052421677.1\|1234324_1237537_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|374168
NZ_CP009280.1\|WP_042133861.1\|1231865_1232501_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042133853.1\|1219464_1221267_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_081969829.1\|1243708_1245556_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213192
NZ_CP009280.1\|WP_039305831.1\|1219015_1219348_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_052421676.1\|1227941_1230365_+\|transcription-initiation-factor-TFIID	unknown	unknown	gnl\|CDD\|372732
NZ_CP009280.1\|WP_042133874.1\|1245528_1246215_+\|ECF-transporter-S-component	unknown	unknown	gnl\|CDD\|377783
NZ_CP009280.1\|WP_042133868.1\|1241265_1241541_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042133863.1\|1233065_1234328_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042133876.1\|1246359_1248069_+\|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl\|CDD\|223910
NZ_CP009280.1\|WP_063779779.1\|1238261_1240595_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP009280.1\|WP_042133855.1\|1224547_1227937_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372732
NZ_CP009280.1\|WP_039305825.1\|1221323_1222247_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225169
NZ_CP009280.1\|WP_042133850.1\|1217774_1218917_+\|3-dehydroquinate-synthase	unknown	unknown	gnl\|CDD\|341474
NZ_CP009280.1\|WP_042133865.1\|1240656_1240893_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042133858.1\|1230558_1231830_+\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238742
NZ_CP009280.1\|WP_052421679.1\|1242854_1243799_+\|energy-coupling-factor-transporter-transmembrane-protein-EcfT	unknown	unknown	gnl\|CDD\|223692
NZ_CP009280.1\|WP_156118532.1\|1222634_1224458_+\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238119
NZ_CP009280.1\|WP_042133870.1\|1241961_1242858_+\|DUF4430-domain-containing-protein	unknown	unknown	gnl\|CDD\|379618

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_052421677.1\|1234324_1237537_+\|hypothetical-protein	gnl\|CDD\|374168	pfam15847, Loricrin, Major keratinocyte cell envelope protein. Loricrin is a family of major keratinocyte cell envelope proteins found in primates. It acts as an important epidermal barrier, and is initially expressed in the granular layer comprising 70% of the total protein mass of the cornified layer. Expression of Loricrin is regulated by TNF-alpha via a c-Jun N-terminal kinase-dependent pathway.	3.74915e-07
NZ_CP009280.1\|WP_042133870.1\|1241961_1242858_+\|DUF4430-domain-containing-protein	gnl\|CDD\|379618	pfam14478, DUF4430, Domain of unknown function (DUF4430). Although this family has overlaps with SLBB, the majority of its sequences are unique. Several family members, eg UniProtKB:A0RGA8, that do not overlap have an LPXTG-cell wall anchor at their C-terminus, a SSF_Family 10_polysaccharide_lyase or Glycosyltransferase structure associated with them in the middle region, as shown by InterPro, as well as this domain at the N-terminus.	1.89209e-19
NZ_CP009280.1\|WP_052421679.1\|1242854_1243799_+\|energy-coupling-factor-transporter-transmembrane-protein-EcfT	gnl\|CDD\|223692	COG0619, CbiQ, ABC-type cobalt transport system, permease component CbiQ and related transporters [Inorganic ion transport and metabolism].	1.77253e-11
NZ_CP009280.1\|WP_052421676.1\|1227941_1230365_+\|transcription-initiation-factor-TFIID	gnl\|CDD\|372732	pfam13809, Tubulin_2, Tubulin like. Many of the residues conserved in Tubulin, pfam00091, are also highly conserved in this family.	0.000387562
NZ_CP009280.1\|WP_042133874.1\|1245528_1246215_+\|ECF-transporter-S-component	gnl\|CDD\|377783	pfam07155, ECF-ribofla_trS, ECF-type riboflavin transporter, S component. This family is the substrate-binding component (S component) of the energy coupling-factor (ECF)-type riboflavin transporter. It is a transmembrane protein which binds riboflavin, and is responsible for riboflavin-uptake by cells.	5.63084e-08
NZ_CP009280.1\|WP_156118532.1\|1222634_1224458_+\|VWA-domain-containing-protein	gnl\|CDD\|238119	cd00198, vWFA, Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains.	6.98647e-19
NZ_CP009280.1\|WP_042133876.1\|1246359_1248069_+\|methyl-accepting-chemotaxis-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	4.39752e-52
NZ_CP009280.1\|WP_081969829.1\|1243708_1245556_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213192	cd03225, ABC_cobalt_CbiO_domain1, First domain of the ATP-binding cassette component of cobalt transport system. Domain I of the ABC component of a cobalt transport family found in bacteria, archaea, and eukaryota. The transition metal cobalt is an essential component of many enzymes and must be transported into cells in appropriate amounts when needed. This ABC transport system of the CbiMNQO family is involved in cobalt transport in association with the cobalamin (vitamin B12) biosynthetic pathways. Most of cobalt (Cbi) transport systems possess a separate CbiN component, the cobalt-binding periplasmic protein, and they are encoded by the conserved gene cluster cbiMNQO. Both the CbiM and CbiQ proteins are integral cytoplasmic membrane proteins, and the CbiO protein has the linker peptide and the Walker A and B motifs commonly found in the ATPase components of the ABC-type transport systems.	1.01153e-84
NZ_CP009280.1\|WP_042133855.1\|1224547_1227937_+\|hypothetical-protein	gnl\|CDD\|372732	pfam13809, Tubulin_2, Tubulin like. Many of the residues conserved in Tubulin, pfam00091, are also highly conserved in this family.	4.57144e-82
NZ_CP009280.1\|WP_042133858.1\|1230558_1231830_+\|VWA-domain-containing-protein	gnl\|CDD\|238742	cd01465, vWA_subgroup, VWA subgroup: Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains. Not much is known about the function of the VWA domain in these proteins. The members do have a conserved MIDAS motif. The biochemical function however is not known.	6.92083e-19
NZ_CP009280.1\|WP_063779779.1\|1238261_1240595_+\|hypothetical-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	6.01437e-09
NZ_CP009280.1\|WP_042133850.1\|1217774_1218917_+\|3-dehydroquinate-synthase	gnl\|CDD\|341474	cd08195, DHQS, Dehydroquinate synthase (DHQS) catalyzes the conversion of DAHP to DHQ in shikimate pathway for aromatic compounds synthesis. Dehydroquinate synthase (DHQS) catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate-7-phosphate (DAHP) to dehydroquinate (DHQ) in the second step of the shikimate pathway. This pathway, which involves seven sequential enzymatic steps in the conversion of erythrose 4-phosphate and phosphoenolpyruvate into chorismate for subsequent synthesis of aromatic compounds, is found in bacteria, microbial eukaryotes, and plants, but not in mammals. Therefore, enzymes of this pathway are attractive targets for the development of non-toxic antimicrobial compounds, herbicides and anti-parasitic agents. The activity of DHQS requires nicotinamide adenine dinucleotide (NAD) as cofactor. A single active site in DHQS catalyzes five sequential reactions involving alcohol oxidation, phosphate elimination, carbonyl reduction, ring opening, and intramolecular aldol condensation. The binding of substrates and ligands induces domain conformational changes. In some fungi and protozoa, this domain is fused with the other four domains in shikimate pathway and forms a penta-domain AROM protein, which catalyzes steps 2-6 in the shikimate pathway.	4.29607e-150
NZ_CP009280.1\|WP_039305825.1\|1221323_1222247_-\|hypothetical-protein	gnl\|CDD\|225169	COG2260, COG2260, Predicted Zn-ribbon RNA-binding protein [Translation, ribosomal structure and biogenesis].	0.00627544

>NZ_CP009280.1|WP_042133861.1|1231865_1232501_+|hypothetical-protein
MKYAEVDSGAPVIAEVVSRVEDRFCTLRWRWPDGVQAVCIHKASAEAPEDEEHPPSGMKLYTREEYKANNGYRDRLDEIGLVAYTIYARLAGNGETLLVRQRDGANKTLVSAGKARIYYSVQHKKGLFSKLKTVHMTITAEVPVPKEVLCYVKKRDGHPASREDGALFPFVQDFAPGRNQLPPIEVGKDDFIRIFFTDGRKYGLYYELVPE
>NZ_CP009280.1|WP_042133858.1|1230558_1231830_+|VWA-domain-containing-protein
MQRKINLLLLLFSLLGGGVAFVLGELLLDRRPYDLPPIVLVGIYFALVALCVSIGSVVAETISPKLNGQSWKLRYLGTSWKMLPLAVVLLFGIGTLTEFVYELNFGGIKPVKNVIMVIDDSGSMLESDPNNSRYEAARALVQQLDEDNKVAVVTFSHEASVVQPLIPLSKAENRQKVSDVISSLVTTEGGTNISGALTEAMNVINEDGADRGAMVILLSDGFSQFDTSTELTAFVDRGIAVNTIGLALDDPSGSNLLQDIASVTGGQYYDVTDANRLGEVFQQIYDRLGDRTLLTERSDRAADSPYYAVVRILALILIGTALGLGLGIIFDNRHLARSFSFGGALSGLAAGLILEFGLNGDTVTDPMIRLLALLVLVAILTLFTYVVPVGEGRLSRKGRAAGAAAAPADGFPPPRRNRGSKGF
>NZ_CP009280.1|WP_052421676.1|1227941_1230365_+|transcription-initiation-factor-TFIID
MIRDQALQYSEQYAAQEEAQHNKGDGRSSIHYPALFLFLGDKVTPAIGPVLERCERKWDNAGGVMALHAGSPSGSGSTQEKDGIKGWIGSGNSSVHERVLHMALPNTAGRDPRTVRRELYREFHEDSQYLAGMNRTLRQLSNSIADYGRLYSSFDVIHLSIVTRVDDPLNVLLPEVALLARAILSQSFKSVQTDLYALINEREQGDNFGYSSSVGLAFLRELDGMQAADYALSAPLLVTEEGLSIPVGHGPSALFDLVYLLSDKNERGLMSVHGMDDNYEIIAHISLLKNRVRPAADHASGHGGYNNMTFKSGIRGSTGRQGYASAGFSAVRRPNRQIALAVLYHALHYLAEKLRAGNSRSLKERQALLGLGADSLRARAAELLPDDTGLAEMTGLMSLGRPSYSELRALSLREAEELLFGEGGQAYFRSNFAEVSTRRTAAIDPAREWAGVLAAEEQATPPVTFYQLAEWTAELAEGGGSVLHALRQHMGGLRSALLSAQEELERLYAESVERQPFQRVPLLDKRTVRNFIHYLFDTVYGKKYEILRLESELALCLRYDAALEQLHADSRAKVLAMEALEEELQSLALASIGRSKDTVDQNIMEYYRSVTEEVMKDIETRRGGNIFFSERFMGSLSELLRRGRDAVAERLIEICRRELLTAGPFTLPFEEELLRRANVAAAYENRGIVSKEELFKQLYRSLEEEAAMNVRLFEYTQEHRHEEKYFFGDSASEFLRYAFGADETTRIYRLGFVHEQRRSGVEKLNLMGGFHLEDLLYYRNGKVYYETYAGNGYELHGLAEEQLPEMR
>NZ_CP009280.1|WP_042133855.1|1224547_1227937_+|hypothetical-protein
MKPVVREHIQQLDVSLGGGIVSDKIRVDTIDNPILIIGLGGTGIDALLRLKYQINRRFKLPEDPLSKKKRDKPDNVEFLAFETNEQDRGKKYKGIGLDPQNEFVLLANAEIGGLLQNRSILDSYITDWLSPELSITDGMNGAAGVRQAGRLLLFTKINQVVAAIDKKIKTLSVGTSKKLMVFLLTGLSGGTGSGAFLDIAYIVRGIIERDYGAAGIDRVNTLGYLFTPDVNLANKSLSEHTREYIRKNGYAALKELDYWMNVDSRGERFRQQYGNILSVNSPLPPFNLCHLISATNTEGKLLENAYDYCMNVTAENITNFMASEEKASGEEFAIHDYISNIRTNIAQMNKTYPANYEYNIIGASSAVLPIEEMTTYLAFRLFDKMDKMFHHAPGQEDVEKMARKLGIDLDTMIKTFESRVPEPLPGYQNSERLSHANVVKNQVVSMDTELEQNFLARAREEYIKAKKQLPGEITGRFGEELERIFLHPEQGPFYVSRLLYTEKGFCILKLIQSYIEALRESLLRLPRDIETAQDSAEEKLGDARSAFVSKEKKKNAYIEAKINEYWLHADVERTEQMIQFYEDLYELLNEENSRIYGVFTEILTALSSIFEKNGDILINGEEQADHKGNKTYYWNIVNVPDISATISKVMDQKDGDDLIRDFTREMLKHSGRWVKEQEIDIVRSISEFLSDKFGDLITRSMEDFLVMKYGREEPLDKFVERIIAGRLDEDAVPIFHLSNSSGSLHFPSWGFVSVPVKAPGILKGIRNYQNNALGKSQFTIKESQVKNRIFWLNTRNGVPLFVYTPLRVFEENYERTILDKEGIGRHLVMTDKDNWTYLPSPIPEKSWGDTYVNARVRDYNARVRADFLRALEAGVIIEKGIDENTSSRFSVIFTKPFDLDKMLSGYDLQLGSSRPNLGEVRKAAEELKALRAGGLEREGIKDIFGSINRELAQENLIRSPQLIARVREELAKYDALSAKAAELEVLVHQHLDEDKWIDQFIEALYTDTITKKGALYVYDRDEDEDAWEPFANLMKERSYVEYAVYRHFRALDEKSRSLLLRKAARRAGEMTAAEDVTPLLYKLEGMYVSFLEARDSLEYERVEHANGDEMYGFYKSLTGKLGSIRRKLK
>NZ_CP009280.1|WP_156118532.1|1222634_1224458_+|VWA-domain-containing-protein
MLRTHRNPRTIKNRLQRIFPVLLLILCIAVLPFGGAAASAASAAPSHIDAVLLIDVSNSMNKSDKNKIANEAMKMFIDMLSTQGDKVGIVAYTDKVQREKALLGITSAGDKQDLKDFIDGLNRGPYTDIAVGMEEAVKVLENGSDPGHEPMIVMLADGNNDLDEASGATQAQSDQELKAAVETAKQKGYPVYTIGLNADGKLNKDILSNLSDQTGGKAFTTDSADDLPQILSEIFASHLKLKVVPVPSITANGDYQEVTVNVPNGSVLEANISIMSSQPVTAKLSDPSGKEVAIPSDAVLLSKSSTYTLIKLLSPEQGDWKLQVKGVAKDKIDINLVFNYDLELKIDVLPSQSYRKGDTVDISSHLFSNGAEVTESSLYQEMKAVLLATDVDTGTVEEIALDNSGAEFKGAFEIKDNHAYELKVRAEESSFYRESDVLTINAKTGTVATSPPATGAGTGEEPVTDQKSPSTLYYIIGGIVLLLAAAAAFWLLRRRSNRGFVGQLVVEVLDGNTGEKTYPQYKKLAGFRGKFTLHQLLQLAPELKESEKLVFTPGNNDRLMLRGGEGISVERSGRAADTSRGLEMKSGDRVSVSLQTVDKTILLEYLI
>NZ_CP009280.1|WP_156118531.1|1222239_1222392_-|hypothetical-protein
MITYVILGVTFLYAVIQISLYASRQRKPLTREDIDERLLAALNGGDSTRE
>NZ_CP009280.1|WP_039305825.1|1221323_1222247_-|hypothetical-protein
MSKKKPVTFRPFKAPRYSYEKLRICRRCGRYTALGEERCTRCGRASLTPVEKQAVSIAGRKMHTRLLLILLLTLASVYFGQSLQQMALSGAGGIVIAGLVYYTQRKVRQNENLYALNELLGRNILRIKEDLELNRQEAVSVLRENDVLAYEKLREISILLRGDRISRQRVALLHGFQLRKDMVLELEQLLLKDFEPLLAEYIGEIAKVRPDLIKDRTLRYVKNYEVQILEMDKGLAILTVVAGAAVRLKRYALLYSGLIGRYVQELPKDRFLRLSRLIAANPYEPWNGLDAKVAEIRELKYRWDPEV
>NZ_CP009280.1|WP_042133853.1|1219464_1221267_-|hypothetical-protein
MTIKQALTLRNIMIILCIFMLVLLGQKALGIEDKIQTVREAERLYAAGELIAAENQYRLAAANTAILYKEEQINARLKELAPITAIRSSLRGLVLTLEDQLTVKDFTGYMESYASLLSLKSKYMVTGGPYEVYYRQLSADSGISEKMTAGFRQFKEQFLAGLTESQKNAANNTTGAGSAESVKWSLLQIPEAYYGGAGAKEELLAAKFEAHDTARLKALAAAGSFQPMLDSALSMEEAYQSHSYTADWIEDQVQESTTLILNKDLDGDRTAAFAGHAVAYRKYAESAGLKSSKVLKLIDSSTTRLLREAARQVRGGQYAEAIRLYGNLNPLQDTSEAVAAATLAWNTAEPVRLLPGGDVQGSYKLTASVTGRYGAKVAVAGVGASGRLVYADMSDDGTLSTRTGDVVADAAALIELTFDESLSVYSEVPVVTAIGSREDGRRTFTAYTIRPEGISQLFSFAGNGYELIAEDGSIRVSDTDLADGQDGQTAIFRQVNGAYEFSEIYREVTYTPIDASQLELHPYEKVTLSCNIYIGSAGRTVASSNGRYLILQGETGGVTGLAVASGQFENGYEHAQTDAGEQYVPVFIVDSIGSLSIQMP
>NZ_CP009280.1|WP_039305831.1|1219015_1219348_+|hypothetical-protein
MGNPLKEFKNSINGLKQSLDGVKQSVDGLKAPVDEFKTNVQETLDEAKSRSEGVKSELGRMKQAVKETQAVLTEVKDTLTASADVLYTRKRYLRLFGRKRKLQTAKAGRA
>NZ_CP009280.1|WP_042133850.1|1217774_1218917_+|3-dehydroquinate-synthase
MSKSFEVVLKKVVDHSYTIEIGEGLFGSLIRDLQQGLLPDVSKFAIITDSTVEPLYGRPLLELLRRSGFQADLFSFPAGESSKTRETKALLEDQLLNQAYGRDCCIIAVGGGAVTDLAGFLAGTFGRGVPALNYATTLLAAADASVGGKTGVNTPVATNLIGVFHQPRKVYIDLAAWRTLPAREFRSGLAETIKHACLADETFFRYLEENIGRVISEQGGLILDADVCGHIALTNCRIKYEVVEQDEHESNLRQILNLGHTAGRALEALSGYQLLHGEAVAVGLVIQARLGVKYGYMTAEQADRVVSLLKKAGLPTEIPDSIANRALVDKMYTDKKVRSGRIRFVFQDGIGEMKRFADGSYSVPVEEADIMELLEEMRGN
>NZ_CP009280.1|WP_042133863.1|1233065_1234328_+|hypothetical-protein
MSFFSRFMKKNQAPARPLYYDIVCPYCFSRFEPEEVVFRAMHSREDDENYALGEDDLLNKYRERFGLDTVDDLEAILNPADIPEEYHHYTDHVLTGITDRYGVLTRRRLCPSCHNELPVTAGKVPSNIISIIGASQVGKSVYMTSLIHTLQHTTAGHFDAACMPLNAEISRKFRTLYEEPLFERGDLLASTQKEKMQEPFIFQFVFKDESKPPLTLVFFDVAGEGMVDQDYLGLHGQHIKNSAGILFMVDPLQIRSIREKIRINFGDRPGEWVSQYDEPRDVVLTMFGDFIAYQEKSKTNIPTAIVLAKSDMLHSLKDEDGDYIKSNSNVFNNYVHRNTLNLDEFHNIDGEIRRFIEKVDRPFKDTMDVYFANTGYFAVSALGSNPVNQKVEGVVSPIRVDEPFIWLLHKLNYIEGSDGP
>NZ_CP009280.1|WP_052421677.1|1234324_1237537_+|hypothetical-protein
MNRFSGSMITQQMYTRERRGVYRATEGFDTVAKSESLDNNFVKKILHPFCLYDAPAELAARGEKDEELYPDALHLFHTESNETVIGLSRYLAADFTGQRSAFFAHNFVVPPIRSEEIVEGYGEWLHAGFARSYEGEPGGTLPELESIPVGVREESADPLTVLRSLGFTEELFKALLQAVMLSVAGKKKIYIALDVPISELSQRAVELTEVLYASMPHDFRRRLGVITYAKEPQSRKYIHLTFVEKGSLRPGDRSIEKDYIFDLAGARILNADFGESRQTYADLAWKTLGQKGGSLRDFARFADSLLLGESVDRKLSLALYNELAVFYEIEQGNEDLYTGNKNAVLGGLLSYLKPEGALESRVRLNDMFLERFDREYDLIRKKGIPAPEILEWFKEYFAMPGHNYRVKIVDYFINGMLNCQSAGREDALAAAYGIIEGNDELSAAFFKRVLAQPIFRKALLEPYMESRLADAPKSADILRFVAHWGRFLPEALQQAFVRDTVKEYLLEKLQRDNDPVAAVASVHESVQKAEKERRRGGGVHAEALSLLQELGTVADRFLLNRISLDELTMEQLLEISFLRYRDTADWQPPLDAIAKCKANALRAAYRWFGEEKPDEEIFAGLSPRELDDVQLLGGRWLKESRSIEPFERLPLAFYHSSEREGGPLDYDALLELVARKAGNDKETVYRFLAWSQHNRLFTISSKKLWPNYRRAVLKYFLKNDREAFKNRDFRKSYSSAATPAMQNVYNEARSQLASPLARWVSRSRFQILISGSVLGIVLIIAVIAISWLRPDADTAAPQPTVSPIRGDIHSADGQEQAPVSVRLVGGVADAGTATGTGNGGTEGTGNAGGAEGGGTEGSGNAGGAEGGGEAGVKLVFSFASVAECSAFNPAEIIVMSGNNVVDTYKVAATASSCLAAGVDGGANGDAAAGNSGGSDKAEASPAAGASGAGNDGGSDEGAAGTDGGATGNEAVGTDGGGDAAAGNSGGSDEAEASPATGASGAGTPARVYEVTVELEPGAKLAAGDVITAGIYTLKLQASPGSILGSTPSTTPETTPGTGPTPSASPDTDAE
>NZ_CP009280.1|WP_063779779.1|1238261_1240595_+|hypothetical-protein
MRNRCKYKQWLCEGNFISAACIVSFPGRPVQGGLYVAPASAEDAGFIYTILFTERGQAMKNNLSSKFIRLGLIVVMMFAVLGAAVAPAGQAFAETAASTGNNAASLPSGTAVSVAEAVYATSEFVLKAGVQSDWQAIGLAQAGYKVPDSYLKALESKVAAAKGVYARATDYARITLTVRALGGNPADVAGYNLIEKLYNNDKITGQTLNNAAYVLLALDSGTYTMPDNAKWTPAKLLAEILSKQNTDGGFTLTTGASDPDMTAMVLTVLAGHKDDPAVNTAGQRAAAWLATAQDKNGGYGDSSESVAQAIIGLSSFGIDPAGAEYTVGNVNLVSKLLSYSAADGGFAHTAGGSYNQLSTEQALEALVAYKLFSTGSKLYDLSNSPVKSPQVSVSVAIESPNGTLAEGTVYAGNVLQALEKAAAAKKVALVNEAGNYVTGIGGVTAGAFGGYDGWMYVVARGGAWIYPSVGMGDFLLAENDRVLVYYGGDNTQVVESVTVSPAQPQPGQDITVKVTQKQWVWNEATFTSDPVSSPAAGVQVSIGGKTAVTDAAGSAVVAGGLPANKYTITVTGYLKDSTPAVVRYSQPLTVASAAADRAAFTDVKSISPWALESVYTAYDRKLMGGVSESSLVFAPKQNITRAEFAALLLRLTGNEPSAASSAQSFSDVKADAWYYGAVNKAKELGIVSGVAGTAFKPDGPVTRQDMAVMIVRALKLDEASAAAGTGKFTDEDQISAYALTAVRTVTGLGIMSGTGGEFAPATAVTREMAAAVAVRLP
>NZ_CP009280.1|WP_042133865.1|1240656_1240893_-|hypothetical-protein
MKYNNLPATTLVRREMLPFVQQFPIIAAILIEMLYFVQDFQQAFGFPPQTRVEIVRFLPQQPYYSNFTAVKTKLYIHI
>NZ_CP009280.1|WP_042133868.1|1241265_1241541_+|hypothetical-protein
MLLMLLMLLMLLMLLMLLMLLMLLMLLMLLMLLMLLMLLMLLLLMLLMLLMLLMLLMLLMLLMLLLVGLELMKLMELLLVGLELMKLPLVG
>NZ_CP009280.1|WP_042133870.1|1241961_1242858_+|DUF4430-domain-containing-protein
MFSLLKSGRARLYPLLLLLVVLLLSGCSKAQPDSAGGGPVPPASSQAAQTPRPEGTAIPSATADGMAASSSGAAPAGAAPGVTEQAPVTQAPVPAATAPAPGHTGAAAPASAATGSPAAPAPAATGSPAAPASAATGSPAAPAPAATAKSAAPAPAATGKPAAPAPAATAKPAAPAPAATAAPVNTVTLSITGDEEHGVILAPAAYEIEKNETALELLGRITRQHKIQMEYQGSKTFAYVEGIDNLYEYDHGAESGWMYKVNGEFPSKASGSWVMKPGDTVEWLYTLDLGKDIGAASP
>NZ_CP009280.1|WP_052421679.1|1242854_1243799_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT
MNSGFQSMYPAVALLYYAGLLLFALLGLHPLFLVTEIAGLLALLLLQGQGKALLRGLPFMLLMGVSVAVLNPLFSHRGAHILFYWLDQPITLEAVLYGLIMMTVLLTIFIWFISYNYTVTTDKFMYLFAAAAPRTALLTLMALRFVPLFQRRLRQITLIQRLRGVDVRTGSLRKRMQDGMTLLKVLLTWSLEEALQTGDSMTARGYGVAKRSTYSIYKPDRQDKLILLVLTLSGMIALFFWLQGYGTLEIYPRMKSMDFGWQDAVMYGSFCLFVLLPAGLEGKEKWLWRSSKRNKYPSAILKKTGTRSMSSRSQ
>NZ_CP009280.1|WP_081969829.1|1243708_1245556_+|ATP-binding-cassette-domain-containing-protein
MVMEILKAEQVSFRYPEEDRDSLHELSFTIEEGEFVVLCGPSGGGKTTLLRHLKRELAPVGMFSGSLTYKGQLLPELPAAVAAGEIGMVFQNPDAQIVMDTVWHELAFSMENLGMPPAVMRTRLAEICGLFGLEPLLYQSVHELSGGQKQLLNLASVLLLQPKVLLLDEPTSQLDPVAAREFIMALQRLNEEMSVTVIISEHRLEEVLPLADRVLMLEGGRLVADAGPRAFVQQAGSASLASRQAYLPAASRLYLALSPEAGTAAAENIPLTVREGKRWVHSRAAVASTVTEAGVCATVIRDHPAANCGAGLPAAVSREETAAAPGTVTPANAGAEPATSPSNSFSQVRNPDSPVKLPAPSAEILLSCREVTFRYDKEGREVLRKLSLTLRRGELLAVMGGNGAGKSTLLHVLGGLMKPQRGKAELSKGSTTGLLAQNPLLYFSYDTVAEELQHMAQYAGASLEEAGREIDALLEVFRLREVLQSHPHDLSGGQQQQTALAMMMLLKPDILLLDEPTKGLDPAAKDRLAALLQQLRRQGASILIVTHDVEFAAKYASRCALLFDGSITAEGAPAEFFSSNYFYTTAVNRMVRDLLPQALTIEDVIRTWSGSAPPC
>NZ_CP009280.1|WP_042133874.1|1245528_1246215_+|ECF-transporter-S-component
MVRFRAPLLIALGLFVAGLALTAALKDRHYVLLSLVLLLAALLPLFLRLERRQLASRELVLLAVLSAIAAVSRIPFAALPGVKPVSAVVILSAYVFGAEAGFVIGAVAALVSNIYFGQGPWTPWQMFAWGMTGLTAGWLRNTWWMKKRPGLLIFGFIWGFLFGWIMNLWVILSLPDAFSWGLVAATYGASFYFDLAHALSNVLFLAILAGGWTKVLKRFRKKYGLLQE
>NZ_CP009280.1|WP_042133876.1|1246359_1248069_+|methyl-accepting-chemotaxis-protein
MRHLKIKHKMTLLIAVIVVLLIGIGTTGIMTTSRMADRSQETYEQNLLPIYLITEIRGNNRAIESFLLEDLITRDAAKSLELKAAIETNITTNNELLEQLKTVEFSNDKIAANINEYLLLLPDYRSQRDNIIHLADNNLNDEGYQVFSGGAFSESRRTMVNLLEDTAALLVQDSSAHNEDTVASAKSSITLSGILITIAWVLSIVISIMITRLITKPLKELQQLMKRAEEGDLTAAASYQSKDEIGQINTSFNTMLEGLQNMMRGVSESAEILSASSEEMSASAEQTAHASQMIAETSSEIAAGFDVQAESIARTARSVRTMTYDINEARHSGSEMNGLMAQAASSTDRGVEAVERILAQMREIDSSVSASQSIVGSLGSLSEEINTIITTINDIATQTNLLSLNASIEAARAGEHGRGFAVVAGEIRKLAEATGRSSLQITEIITHIRQQTESAVESMELGSGIVSHGVAQSEVVSAAFTEIQTSIQAASEQMELITEVIGHVAQESEGVAQAMAEVDEISRKGAGDVQDTSAASEQQLTAMGEMSSSAQYLATLAEDLQKHLARFKL

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_CP009280_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_2

1307950-1308026

Orphan

Consensus_repeat	Method
TGGGCCAATGGAGGAAATGAGGGGCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_2

>merge|NZ_CP009280|2|1307950-1308026|CRISPRCasFinder
TGGGCCAATGGAGGAAATGAGGGGCATTAGTGCTCTTGATTCCACCGGATGTGGGCCAAAGGAGGAAATGAGGGGCA

>NZ_CP009280|2|2|1307950-1308026|CRISPRCasFinder
TGGGCCAATGGAGGAAATGAGGGGCA	TTAGTGCTCTTGATTCCACCGGATG
TGGGCCAAAGGAGGAAATGAGGGGCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042133951.1\|1298684_1300184_+\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP009280.1\|WP_042133953.1\|1300149_1301529_+\|oligosaccharide-flippase-family-protein	unknown	unknown	gnl\|CDD\|240533
NZ_CP009280.1\|WP_156118536.1\|1320210_1320696_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275056
NZ_CP009280.1\|WP_042133975.1\|1317205_1318684_+\|potassium/proton-antiporter	unknown	unknown	gnl\|CDD\|235410
NZ_CP009280.1\|WP_042133969.1\|1308563_1309937_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|273648
NZ_CP009280.1\|WP_042133962.1\|1305055_1306156_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340833
NZ_CP009280.1\|WP_042133981.1\|1320932_1321619_+\|M50-family-metallopeptidase	unknown	unknown	gnl\|CDD\|315961
NZ_CP009280.1\|WP_042133978.1\|1319453_1320158_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224924
NZ_CP009280.1\|WP_042140779.1\|1295586_1296522_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|366154
NZ_CP009280.1\|WP_081970412.1\|1312223_1312625_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214807
NZ_CP009280.1\|WP_042133982.1\|1321806_1322490_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042133957.1\|1302626_1303817_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP009280.1\|WP_039302998.1\|1297879_1298653_+\|WecB/TagA/CpsF-family-glycosyltransferase	unknown	unknown	gnl\|CDD\|377136
NZ_CP009280.1\|WP_042133976.1\|1318915_1319371_+\|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl\|CDD\|153102
NZ_CP009280.1\|WP_042133965.1\|1306160_1307501_+\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|223936
NZ_CP009280.1\|WP_042133971.1\|1312836_1314351_+\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|366944
NZ_CP009280.1\|WP_042133955.1\|1301785_1302640_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133005
NZ_CP009280.1\|WP_042133973.1\|1314571_1317118_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366285
NZ_CP009280.1\|WP_042133950.1\|1296536_1297883_+\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP009280.1\|WP_042133960.1\|1303813_1304953_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042133951.1\|1298684_1300184_+\|O-antigen-ligase-family-protein	gnl\|CDD\|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	1.35307e-08
NZ_CP009280.1\|WP_042133953.1\|1300149_1301529_+\|oligosaccharide-flippase-family-protein	gnl\|CDD\|240533	cd13128, MATE_Wzx_like, Wzx, a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Escherichia coli Wzx and related proteins from other gram-negative bacteria are thought to act as flippases, assisting in the membrane translocation of lipopolysaccharides including those containing O-antigens. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	2.34756e-35
NZ_CP009280.1\|WP_156118536.1\|1320210_1320696_-\|hypothetical-protein	gnl\|CDD\|275056	TIGR04211, hypothetical_protein, SH3 domain protein. Members of this protein family have a signal peptide, a strongly conserved SH3 domain, a variable region, and then a C-terminal hydrophobic transmembrane alpha helix region.	3.8525e-07
NZ_CP009280.1\|WP_042133975.1\|1317205_1318684_+\|potassium/proton-antiporter	gnl\|CDD\|235410	PRK05326, PRK05326, potassium/proton antiporter.	0
NZ_CP009280.1\|WP_042133969.1\|1308563_1309937_+\|cupin-domain-containing-protein	gnl\|CDD\|273648	TIGR01479, Mannose-1-phosphate_guanylyltransferase, mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase. This enzyme is known to be bifunctional, as both mannose-6-phosphate isomerase (EC 5.3.1.8) (PMI) and mannose-1-phosphate guanylyltransferase (EC 2.7.7.22) in Pseudomonas aeruginosa, Xanthomonas campestris, and Gluconacetobacter xylinus. The literature on the enzyme from E. coli attributes mannose-6-phosphate isomerase activity to an adjacent gene, but the present sequence has not been shown to lack the activity. The PMI domain is C-terminal. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides].	2.53953e-73
NZ_CP009280.1\|WP_042133962.1\|1305055_1306156_+\|glycosyltransferase	gnl\|CDD\|340833	cd03804, GT4_WbaZ-like, mannosyltransferase WbaZ and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. WbaZ in Salmonella enterica has been shown to possess mannosyltransferase activity.	1.34343e-145
NZ_CP009280.1\|WP_042133981.1\|1320932_1321619_+\|M50-family-metallopeptidase	gnl\|CDD\|315961	pfam13398, Peptidase_M50B, Peptidase M50B-like. This is a family of bacterial and plant peptidases in the same family as MEROPS:M50B.	1.92647e-30
NZ_CP009280.1\|WP_042133978.1\|1319453_1320158_-\|hypothetical-protein	gnl\|CDD\|224924	COG2013, COG2013, Uncharacterized conserved protein [Function unknown].	0.000271017
NZ_CP009280.1\|WP_042140779.1\|1295586_1296522_+\|glycosyltransferase-family-2-protein	gnl\|CDD\|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	5.94947e-29
NZ_CP009280.1\|WP_081970412.1\|1312223_1312625_+\|hypothetical-protein	gnl\|CDD\|214807	smart00758, PA14, domain in bacterial beta-glucosidases other glycosidases, glycosyltransferases, proteases, amidases, yeast adhesins, and bacterial toxins.	8.39807e-25
NZ_CP009280.1\|WP_042133957.1\|1302626_1303817_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	4.4152e-65
NZ_CP009280.1\|WP_039302998.1\|1297879_1298653_+\|WecB/TagA/CpsF-family-glycosyltransferase	gnl\|CDD\|377136	pfam03808, Glyco_tran_WecB, Glycosyl transferase WecB/TagA/CpsF family.	1.04844e-86
NZ_CP009280.1\|WP_042133976.1\|1318915_1319371_+\|DNA-starvation/stationary-phase-protection-protein	gnl\|CDD\|153102	cd01043, DPS, DPS protein, ferritin-like diiron-binding domain. DPS (DNA Protecting protein under Starved conditions) domain is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. Some DPS proteins nonspecifically bind DNA, protecting it from cleavage caused by reactive oxygen species such as the hydroxyl radicals produced during oxidation of Fe(II) by hydrogen peroxide. These proteins assemble into dodecameric structures, some form DPS-DNA co-crystalline complexes, and possess iron and H2O2 detoxification capabilities. Expression of DPS is induced by oxidative or nutritional stress, including metal ion starvation. Members of the DPS family are homopolymers formed by 12 four-helix bundle subunits that assemble with 23 symmetry into a hollow shell. The DPS ferroxidase site is unusual in that it is not located in a four-helix bundle as in ferritin, but is shared by 2-fold symmetry-related subunits providing the iron ligands. Many DPS sequences (e.g., E. coli) display an N-terminal extension of variable length that contains two or three positively charged lysine residues that extends into the solvent and is thought to play an important role in the stabilization of the complex with DNA. DPS Listeria Flp, Bacillus anthracis Dlp-1 and Dlp-2, and Helicobacter pylori HP-NAP which lack the N-terminal extension, do not bind DNA. DPS proteins from Helicobacter pylori, Treponema pallidum, and Borrelia burgdorferi are highly immunogenic.	5.38282e-58
NZ_CP009280.1\|WP_042133965.1\|1306160_1307501_+\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	gnl\|CDD\|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0
NZ_CP009280.1\|WP_042133971.1\|1312836_1314351_+\|glycosyl-hydrolase	gnl\|CDD\|366944	pfam02156, Glyco_hydro_26, Glycosyl hydrolase family 26.	1.71848e-51
NZ_CP009280.1\|WP_042133955.1\|1301785_1302640_+\|glycosyltransferase-family-2-protein	gnl\|CDD\|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	7.71228e-63
NZ_CP009280.1\|WP_042133973.1\|1314571_1317118_+\|hypothetical-protein	gnl\|CDD\|366285	pfam00754, F5_F8_type_C, F5/8 type C domain. This domain is also known as the discoidin (DS) domain family.	1.24111e-14
NZ_CP009280.1\|WP_042133950.1\|1296536_1297883_+\|O-antigen-ligase-family-protein	gnl\|CDD\|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	6.58917e-08
NZ_CP009280.1\|WP_042133960.1\|1303813_1304953_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	1.86737e-52

>NZ_CP009280.1|WP_042133965.1|1306160_1307501_+|UDP-glucose/GDP-mannose-dehydrogenase-family-protein
MKLAVIGTGYVGLVSGVCFTLNGNHVICVDKDEAKIEKLNRMESPIYEPGIEALIEMNLREGRLSFSADLKDSVRRSDIVILAVGTPSLPGGEADLRYIEGAAIEIAQAMEGYKVIMTKSTVPVGTNEKIRNLIASHTNHPFDIVSAPEFLREGSAIRDTLHPDRIVIGLDNPELEPMMRQLHQGFTDNVFVTDIRSAEMIKYASNAFLATKISFINEIANICEKVGADVTEVAEGMGMDRRIGSTFLQAGIGYGGSCFPKDTNALIQIAGNVDYEFKLLKSVVEVNKGQRFMIISKLHESLGSLRGAVIGIWGLAFKPNTDDVREAPAREIVEALVAEGATVKLYDPIAAENFRAQYDHPQLRWCGLAEEAAEGSDAVCLLTDWSQFKDIDLHLLAKSMRRQVLIDGRNVYSKEQIEGTGLEYHSVGRPQMGGLSGFSASVAGAV
>NZ_CP009280.1|WP_042133962.1|1305055_1306156_+|glycosyltransferase
MKIAIAHDYLIQMGGAERVVEVFHHMYPDAPIFTTVFNGSRLTDNLKDADIRASWLQKIPGVKRNFKGVLPLYPMAVRDLDFSGYDIVLSSSSAFMKSIQVPESTFHLCYCHTPMRFAWDYDTYMERQSNSGLFKRLLKVYMQRLKNWDQRTSKNVNQFVANSSVVKTRIQNYYHRDSDVIFPPINTARFTSSPTIGDYYLIVSRLVSYKRIDLAVEAFNRNGVKLYIVGDGPDRKRLEGMAKDNISFLGRLEDEEVTGLMSQCRAFVFPGEEDFGITPLEANAAGRPVIAYQAGGALDTIIPYVNGVFFQHQEVDDLLQAIDEAESYAWDIEQIMGHARKFDEQAFMVQFKQYVEQAYVNFLKGG
>NZ_CP009280.1|WP_042133960.1|1303813_1304953_+|glycosyltransferase-family-4-protein
MIKVAYIDHTAKWSGGEVALFNILTNIGEQISPLVILAEEGTLAERLREKGIDVRIIPLDESIRSRGRNAVNLGAPAAAMKLLAYGRKLAPLLKEEKVDCVHTNSLKSAFYGAVAAKKAGVPLIWHIRDHIGAPYLKPVVAKAIRLLSRLLPNGVIANSHSTLNALELPRSKKTLVVYSAFAKAIGEGIGKRDQKDFNVLLVGRLAHWKGQHIVLEAAKAFKHDSRVKFWLAGDALFGEEEYKQELIQQMQQGNITNVSLLGHVDDIQGLMNKADLLIHTSITPEPFGQVIVEGMAAGLPVIASNEGGPVEIVVPGVTGMLIQPGDATVLADSITWMLNHPEERRRMADNGMKRVKEHFVIENTVKDIVAYYKGLLAVT
>NZ_CP009280.1|WP_042133957.1|1302626_1303817_+|glycosyltransferase-family-4-protein
MSYNDGLNIMTTGLSWPSLQPGGLNTYFKSVCEQLSSRNQVHALICSQETPATPKELIIHNAGDPKETIWKRKDAFQRKAADLMGDGSGRIDILYTHFAPYGIGPAIEAKKRGIPVVMTFHGPWNEEMKIEGQGIRHKVKTTIAKSIEHKAYKLADKFIVLSEYFRGMLHDLHGVPLHKIIVIPGAANVERFVPSTNRLAIRRTLNLPEGATTVLTVRRLMNRMGLLQLLEAWKQVAERFPNAILLIGGKGPLRGELEEKIADYGLGNKVRLLGYIPDHELASYYQAADMFVVPSQALEGFGLITVEALASGLPVMATPVGGNKEILQGFRPELLFKSAGSDDMAEGMIHMLSNRKLLPGRDECRNHVLEKYTWQHVGDQVESVFLETLGKGVSVG
>NZ_CP009280.1|WP_042133955.1|1301785_1302640_+|glycosyltransferase-family-2-protein
MDSMTSVLGGRGSYPISAVIIAQDDEVRISAAIQSCRLFADEVVVIDGGSKDGTVQLSESLGCRVYVNPWPGYAKQREFGVERAVHDWVFLIDTDEVVSEELARDILERKPGLTDATVAFSLYRIGDFLGKWLDKGEYLVRLYNRKEYGIRNSLVHEMPEVSEERTVKLNGTLWHQGFRSINDHVARFNKYTDLEAQSAFESGKPFKLSHLLLRPPARFLQKYFVHGLFKKGISGFAVSIFWVMYEFMVGFKHYELHSSGKLTRHNAMGQADKENKGERSYVVQ
>NZ_CP009280.1|WP_042133953.1|1300149_1301529_+|oligosaccharide-flippase-family-protein
MQQLNAKSLPASTVWSSLRRFTKSKDNSSAAVKTMFVSVLILLVNMLTGVLTARYLGPTGRGEQTAMVNWSQFLAFSMSFGIPSALIYNAKKNPDEAGVLYRVALLIGLVFGTMAMIIGIIVLPYWLKSFSHDVVVFAQWSMILCPLIVVSQVNNAAFQFRGDYKTFNWLRYLIPLLTLAAIGILILTGHMNPYTTALAYLVPSVPLFIGMTVSLLRTYKVKLRDAYLNFKRLFTYGMGSYGNDLLGQFSYYIDQIIIAGLLRPADLGLYAVAVSLSRMVNFFSNSITVVLFPKASEMSKDEAVALTFKAFRISTTCTLLGAVFLMLVAPFVIPLLYGKDFNTALTVFRLLLLEVTISGGTLILAQVFMALGKPKFVSILQGVGLILVIPLLFLLVPKFGLFGAGVAMLSSAVLRFLFIILNIRYNLKVKLPRLLINAQDLQWLKTTMNSYIRKKPMDV
>NZ_CP009280.1|WP_042133951.1|1298684_1300184_+|O-antigen-ligase-family-protein
MKMLSRDENSLSLPSRSAVKSAAVMTMICGAAVILPLLIGFASAKLSSSNSLQGVILAGILFPAFLLALLNTRMLIPYTLLIWAVAPELRRIADWYEGVYHSVSLLSLAPLLTGATLAIPVLKEIHKIRKSSTRILLLFSIALAYGAMIGLAKNGIGSVYDLANYIVPLLLIPFFAVTQYKPKDIDRLLYAFANIAVLVAAYGIVQYLTVPPWDAFWMRNADMMSIGTPYPLEIRVFSTLNSPGPAATFLVFALVPMILEKRWQGTLRWIGVLLVVVCLLTTLVRSAWLVLLVMLLVYIASSPSKGKWKTLLQLGFVAAALFTIVPKLPGAEGLVARMETLTSVQEDHSYNERLSLWTNMLPMVAGNPVGQGIGSVGQGTKIGNGGELGEYGNMDNGVIALLLTFGVLGALFFFGALGAVIKEIAVRVTSKDHLQPYARLSLAAWMGAVVSLVSDNGFPGLKGYLIWMLIGLGLSAKEITQSRKKGIPHAAVERKITSR
>NZ_CP009280.1|WP_039302998.1|1297879_1298653_+|WecB/TagA/CpsF-family-glycosyltransferase
MNQVNMFDVNFDNYDFMDLLDYIDKTIQERNQSYILTCNVDHVIKLRKDKEFQEVYSEAGAVVADGMPLIWASKMLGKPLKQKVSGADLFSRLGNAFEQRKYRLFFLGSAEGVPEQATKNLKAAYPGINVVGCYSPSYGFEHNEEENQRIIQMLTESQPDIVFVGVGAPKQEKWIYRHYTSYQAPISIGVGATFDFLSGSVKRAPDFMQRTGMEWLWRLSQEPGRLWKRYLVDDAQFLVLLLKELRKRDKVKNSKSQ
>NZ_CP009280.1|WP_042133950.1|1296536_1297883_+|O-antigen-ligase-family-protein
MTNFEWGSKINALPYGMLYLMSALFLGAAVIYQPVIAVAAVLLIMLLFVSISRPELISYFVLLTTAVSINFLFSGSMFGVEILSLYKLVILVLLVPCILVNGLKFRLSQPLWAMLALVFITFTFSIWLPEMSSSIAVKAFIGLSLPFVFLLINWKKEVAEKQIRIITLLPLVSVLAGVVLQAAHLHSLLDIEFTGAVRIQGANIPAHLAMLAFMGVAIAFIEIKRSPQHIRFYYTMLGLNFLILIGTGTRGPILALVLMVLYYFYDISRQYLKGKTKFLIPLLCSLLVITSAVYLQLDNIKKRSFERTTETGVDLSGRAEAWEYFLNKAEDSPYAGRGLGAVTVANDGSLYKGFVVPHNEYIRFYFDGGYFGAILLLLSLLAVFLLVYRALAPPVKPYYLLFIAAFLIYSFTDNTLSTVQFIIPFCWYLNCLYRSSQLADSPQKEVIR
>NZ_CP009280.1|WP_042140779.1|1295586_1296522_+|glycosyltransferase-family-2-protein
MLVHGEVPKISIIICTYNRSALLVKTLHSLLPLENLDHAEIIVVDNSSKDDTAAAIRRFIDTYGADMDIRYLLEPVQGLSAARNTGILASKSPLIAFLDDDAIPCRTWISTIVSTFEQKPEVMAMGGKIAPIFESKRPEWLIKPFELPYTIVDLGNRIREYPKRLHPCGANMAMRKIVFDISLFPLELGRKGDSLLSGEETWLFGQIQQEGHSILYHPEMAVDHFVPANRLTEDWIMKRYYSQGISNAMKSEGMKGNLLLLGKTGAKVMYILADSILSRSQGRRLLNKCRLESIRGTLHMIWNRKRESAAG
>NZ_CP009280.1|WP_042133969.1|1308563_1309937_+|cupin-domain-containing-protein
MKLVLLSGGSGKRLWPLSNDSRSKQFLKVLESPAGEPESMVQRVWRQLQETGMAESSYLATGRSQVEMIQSQLGSGVPIIVEPERRDTFPAIALTAAYLYSVAGVSPSETVAILPVDPYVESSFFETVLQLESTMLESGANLALMGVVPEHASEKYGYIIPTSAEAGASGYLQVSHFQEKPDRKQAEELISRNALWNCGVFAFRLGYLLDILQRKGLPLNYEELQKQYKLLASISFDYEVVEKEENIVVQPYAGFWKDLGTWNTLTEEMTSNHVGKGFVTADSEGTCLINELDIPITVIGAKDLIIAASPDGILVTHKAESPRIKEVLKSFEQRPMYEERRWGHYKVIDYVKYAEGNEVLTKRIFISEGKNISYQLHHKRSEIWTIVSGEASIVLNEKMHNVKAGDVVRIPEGTKHAILALTDMEFIEVQTGSELVEEDNIRITLDWEDIALQQFIS
>NZ_CP009280.1|WP_081970412.1|1312223_1312625_+|hypothetical-protein
MTLSGAPAVVRTDAVLDFNWRQGTPDAAIGIDFFSVRWSGKLKPLYTETYQIYTTSDDGIRVRINGELVIDSWMKQSGTERTGSISLTAGQLYDIQVEYYENQGDARARLMWESSSQVKATVPASALFLPSAS
>NZ_CP009280.1|WP_042133971.1|1312836_1314351_+|glycosyl-hydrolase
MNTYRKYRLYTTIIPIILILSLLPWGEARSLPVARPVNTPAASIQPVNPSASKEATALLSYLADLSGKGMISGQHDYLESPDEFNNKLKNASGQYAVLHGYELGAINNQSKETIARQRQAVVDSAIKWHKGGGIVAMTFHQNLPGTSPEWANVKMNLSQDKFDAYVTPGTPQYKALIAELDEVAGYLGELRDAGVPVLWRPYHEMNGNWFWWGQKDNFAQLWDIVYDRMVNTHKLNNLLWVWNPNAPNEWAKAYSNYYPGAAKVDVLAADIYNNDFKQSYYENLLKLADGKPIGIGESGELPDPVILSQTQSKWVYTMTWGKMLLENNNLQKIQSFMSNKYTVSRDDYKLALSAQLNALTAVSRNGLKGQYFGNTELSGKPLLTRNDNRIDFNWHGDSPAPGIGKDSFSVRWTGKIKPVYSEKYTFTASSDDGIRVWIGGKLIIDSWKKQSGVSREGSITLTAATAYDIKVEYYENHGDASVRLMWQSPRQKQAVIPQNALTLP
>NZ_CP009280.1|WP_042133973.1|1314571_1317118_+|hypothetical-protein
MSELSAAKDAGPAVPEGTVLWKLGQHDGSAAEFTAAGSNGAKGVFSVASTAVKAAELQSIPSGLHGATNPELRITYKLDKIPVNGVLFRVSILDAYKSVPQMSVFSNRQLSGIIQIAGVDGTDSKYDFRKTYELYIPKEQLISGTNELTLRAARGIYSSAAEDKYNWWTWDNLSLEALKTPVKEPIHGSYTLTGTMVNNKQFYFDKGAVTHLPYIMKWLGLAYSGNIMRTSCASDVGRSCENMGEYYEVLKDYNMQAVALYLYTGDIKLKEDGSLPDDAEKKLTDYFKQYGQYFQYYEVDNEPGLFNRSKAVNLAIADWLNKKGKTIAPHLQTVAPGWAYWPGYSEDSCGNQKGTLKQCGDPDGWERDPEQRNELEEVTDLTNGHSYGESYIFSNGGSFTENLKTFGGAVDGLSKKMLTTEFGTSDSHVDAYQYGASERTAAVFDRIMRGHIGYADMFVQHAAFFKNFSLFKYGFNLEEHDPGATEIYYTKEGEDSRVSIMRRLDLAYATHGAPLSYQITNKDDLADKLVYVRAVDTSTLEPLAGSGATSNKLLVNFVNFEETEQTVKVKVTMPEKTVYEGERFGRGDTYEEARSYMSGRNATPVLEFTETLAPGEAVQYILQPSSEVADVAPQGFKAAAVKGLSMHLSWLEAPGASYEVLRADGPGSELKVIAAGVQSTEYTDSKLQEGTLYTYAVRVSGSGVMSEKTQITATGLVPLDRTGWKVTSNVNTAASKPESAIDGDRRTRWDTGKHQASGEYFQIDLGAVHAIEAIELIYTLSSYDYPRGYTVQVSDDAKSWTQVASGKGKLELTRIAFSQVQTRYIRIQQTGSGGNYWSIQELQVYSRE
>NZ_CP009280.1|WP_042133975.1|1317205_1318684_+|potassium/proton-antiporter
MTHLADQIILLLAALLLVGVLSTKFSTRFGMPALVLFIAAGMVLSHFIYFNNASLTQIAGIFALVVILFEGGMQTSMKDIRPVMKPALSLATAGVLVTTGVVGVFARFILGVPWAESFLFGAIVGSTDAAAVFSVLGGKNIDKRLTSTLEAESGSNDPMAVFLTVSLIEWIQHPDTAIWSLVLSFFWEMGIGLLLGILIGKLATYLINRINLDSTGLYPVMAIGFAVLTYGVSAMVHSSGLLAVYVMGLVLGNSELMYHRTIMNFNHGFAWMMQIAMFILLGLLVFPQELADIAWQGILLSVILMVVARPAGVFISLLFAKFSFREKTLISWAGLRGAVPIVLATYPLLAGLPQGRLFFNVVFFVVLTSAVIQGTTISPLASRLRLVGREDASQPSLMELVALGKTDSEFNHIGIDRHMPIAGMQIAQIGLPDDILFTAIIRNKSIVTPHGSTVIEPGDTVYVLSPKTKRDEMRAIFRSGKGKAAETDITSV
>NZ_CP009280.1|WP_042133976.1|1318915_1319371_+|DNA-starvation/stationary-phase-protection-protein
MSTQVKSHTELHAALNRQTANWTLLGVKLHHYHWYVSGAQFFTLHEKFEELYNEAAGYVDELAERLLAIGGQPASTMTQYLALSGLKEATGGESAKEMVAQLVKDFTAVAEELKQAISAAEELSDQPTADLLIGIRTSVEKTSWMLNAYLA
>NZ_CP009280.1|WP_042133978.1|1319453_1320158_-|hypothetical-protein
MNVDVQDEGDSGSGQAVAFTVAENEEVHVLHPQQIIAYQGPSSGRADRLMDVKGMYRKRKLIRSDITGPCRFVAALPPGYRVKTLQLDGKSDLLYDFRHLFFYSKGVTMQTRVLNMKNMLITRDIVKVKFSGHGSIGILTEGTVCEAELDPFDPLYVDAGSIIAYPENARLELTVYGNHLASQHMSYHWKMTGHGPVLFQAGRQSRRFQRDNNEDGIIKRFLREALPFGGVFIK
>NZ_CP009280.1|WP_156118536.1|1320210_1320696_-|hypothetical-protein
MIKLLGSALLLLGISFTYDIPAAKANYFTDLYNGLQSFSELPGEVNKLQESYQQTAEELQKTKAELGTAVDELGQTKDQLDQSLQQMATYQAQNAALQEQNRQLSQVVDELKNDRTARENYYNRIKVTVITGLALILGYFLLIRLLRFTMRHRSRRSDRLR
>NZ_CP009280.1|WP_042133981.1|1320932_1321619_+|M50-family-metallopeptidase
MNKWLKTLLFLAGSALLTRFIPFSSLFRNLDTMFHEFGHALVTLLLSGSVLRIELHPDHSGVTYSAIAAGGRAILVSLAGYPLASLFSLLLFYLYSRDKRQWGLIMASGVALVMLVLYVRGGFGMIWLSGFILLNAAMLFLWPKVSKYYYLFLAFLTLEESVMGTLFLVTASVLTPSRAGDAANLARLTPLPAILWALLFFLFSLLCAKWALGFFFREEKKANRARSL
>NZ_CP009280.1|WP_042133982.1|1321806_1322490_+|hypothetical-protein
MQASIQPIFTWSQDRILAGGAKNIILLVEWKGVSQGEEFRKKSRKVVAREIELRVWLESHVTVTGCYGCTAEEGEGRSLLLKLGKIHSGQRRFIALEFTMSGMPAGIHEALWLQWQYRQPTVERIRELPLKKLGMEYSHHTDVLGAQCCFHVEKHVELLKMEGLLAEREVARAQNQQQVSTEKLRRQADKLLLLAARSGDMQLVKEAEALYKQLEVEMTLLGKVVTR

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_CP009280_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_3

1420306-1420408

Orphan

Consensus_repeat	Method
CCCCAAGGCTGATCAACCGCAAAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_3

>merge|NZ_CP009280|3|1420306-1420408|CRISPRCasFinder
CCCCAAGGCTGATCAACCGCAAAATAACCCCACAAAGTGGGGCTCTGGCTTCGATGATTACTCAGGTACTTTGCGGGGACCCCAAGGCAGATCAACCGCAAAA

>NZ_CP009280|3|3|1420306-1420408|CRISPRCasFinder
CCCCAAGGCTGATCAACCGCAAAA	TAACCCCACAAAGTGGGGCTCTGGCTTCGATGATTACTCAGGTACTTTGCGGGGA
CCCCAAGGCAGATCAACCGCAAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042134094.1\|1425600_1426194_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_081969841.1\|1413785_1414520_+\|ZIP-family-metal-transporter	unknown	unknown	gnl\|CDD\|223505
NZ_CP009280.1\|WP_081970421.1\|1414523_1414667_+\|S-layer-homology-domain-containing-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP009280.1\|WP_042134096.1\|1427489_1428926_+\|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl\|CDD\|224089
NZ_CP009280.1\|WP_042132671.1\|1415260_1416553_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP009280.1\|WP_039302038.1\|1426297_1427248_-\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|183067
NZ_CP009280.1\|WP_039302057.1\|1418238_1419228_-\|glyceraldehyde-3-phosphate-reductase	unknown	unknown	gnl\|CDD\|381377
NZ_CP009280.1\|WP_052421691.1\|1429286_1429958_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239632
NZ_CP009280.1\|WP_042140795.1\|1424641_1425262_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|341387
NZ_CP009280.1\|WP_042134089.1\|1421168_1422347_+\|YsnF/AvaK-domain-containing-protein	unknown	unknown	gnl\|CDD\|378207
NZ_CP009280.1\|WP_042134091.1\|1422792_1423788_-\|class-II-fructose-bisphosphatase	unknown	unknown	gnl\|CDD\|236536
NZ_CP009280.1\|WP_042134079.1\|1409086_1410403_+\|amidohydrolase	unknown	unknown	gnl\|CDD\|238623
NZ_CP009280.1\|WP_156118543.1\|1410567_1413429_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP009280.1\|WP_042134085.1\|1419387_1420233_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380391
NZ_CP009280.1\|WP_042134081.1\|1416761_1417055_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042134098.1\|1430164_1430725_-\|adenylyl-sulfate-kinase	unknown	unknown	gnl\|CDD\|223603
NZ_CP009280.1\|WP_042134083.1\|1417174_1418083_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381312
NZ_CP009280.1\|WP_042134087.1\|1420483_1420795_-\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP009280.1\|WP_081969839.1\|1407661_1409074_+\|Zn-dependent-hydrolase	unknown	unknown	gnl\|CDD\|236456
NZ_CP009280.1\|WP_039302045.1\|1423822_1424623_-\|kinase/pyrophosphorylase	unknown	unknown	gnl\|CDD\|377080

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042134089.1\|1421168_1422347_+\|YsnF/AvaK-domain-containing-protein	gnl\|CDD\|378207	pfam09557, DUF2382, Domain of unknown function (DUF2382). This entry describes an uncharacterized domain, sometimes found in association with a PRC-barrel domain pfam05239 which is also found in rRNA processing protein RimM and in a photosynthetic reaction centre complex protein). This domain is found in proteins from Bacillus subtilis, Deinococcus radiodurans, Nostoc sp. PCC 7120, Myxococcus xanthus, and several other species. The function is not known.	1.36489e-38
NZ_CP009280.1\|WP_081970421.1\|1414523_1414667_+\|S-layer-homology-domain-containing-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	2.22176e-06
NZ_CP009280.1\|WP_042134096.1\|1427489_1428926_+\|PLP-dependent-aminotransferase-family-protein	gnl\|CDD\|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	4.18184e-124
NZ_CP009280.1\|WP_042132671.1\|1415260_1416553_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	2.79457e-179
NZ_CP009280.1\|WP_039302038.1\|1426297_1427248_-\|EamA-family-transporter	gnl\|CDD\|183067	PRK11272, PRK11272, putative DMT superfamily transporter inner membrane protein; Provisional.	8.64958e-26
NZ_CP009280.1\|WP_039302057.1\|1418238_1419228_-\|glyceraldehyde-3-phosphate-reductase	gnl\|CDD\|381377	cd19151, AKR_AKR14A2, Salmonella enterica aldo-keto reductase (AKR) and similar protein. Salmonella enterica AKR is a founding member of aldo-keto reductase family 14 member A2 (AKR14A2).	0
NZ_CP009280.1\|WP_052421691.1\|1429286_1429958_+\|hypothetical-protein	gnl\|CDD\|239632	cd03577, NTR_TIMP_like, NTR domain, TIMP-like subfamily; TIMPs, or tissue inibitors of metalloproteases, are essential regulators of extracellular matrix turnover and remodeling. They form complexes with matrix metalloproteases (MMPs) and inactivate them irreversibly by non-covalently binding their active zinc-binding sites. This group contains domains similar to the TIMP NTR domain, which binds MMPs. Members of this group may or may not function as MMP inhibitors.	1.03578e-10
NZ_CP009280.1\|WP_042140795.1\|1424641_1425262_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|341387	cd04617, CBS_pair_CcpN, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains of CcpN repressor. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	4.37001e-60
NZ_CP009280.1\|WP_081969841.1\|1413785_1414520_+\|ZIP-family-metal-transporter	gnl\|CDD\|223505	COG0428, COG0428, Predicted divalent heavy-metal cations transporter [Inorganic ion transport and metabolism].	6.90634e-34
NZ_CP009280.1\|WP_042134091.1\|1422792_1423788_-\|class-II-fructose-bisphosphatase	gnl\|CDD\|236536	PRK09479, glpX, fructose 1,6-bisphosphatase II; Reviewed.	0
NZ_CP009280.1\|WP_042134079.1\|1409086_1410403_+\|amidohydrolase	gnl\|CDD\|238623	cd01298, ATZ_TRZ_like, TRZ/ATZ family contains enzymes from the atrazine degradation pathway and related hydrolases. Atrazine, a chlorinated herbizide, can be catabolized by a variety of different bacteria. The first three steps of the atrazine dehalogenation pathway are catalyzed by atrazine chlorohydrolase (AtzA), hydroxyatrazine ethylaminohydrolase (AtzB), and N-isopropylammelide N-isopropylaminohydrolase (AtzC). All three enzymes belong to the superfamily of metal dependent hydrolases. AtzA and AtzB, beside other related enzymes are represented in this CD.	9.96619e-128
NZ_CP009280.1\|WP_156118543.1\|1410567_1413429_-\|hypothetical-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	1.45924e-08
NZ_CP009280.1\|WP_042134085.1\|1419387_1420233_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|380391	cd06986, cupin_MmsR-like_N, AraC/XylS family transcriptional regulators similar to MmsR, N-terminal cupin domain. This family contains bacterial proteins containing an AraC/XylS family helix-turn-helix (HTH) DNA-binding domain C-terminal to a cupin domain, and may be possible transcriptional regulators. Included is MmsR, a bacterial transcriptional regulator thought to positively regulate the expression of the mmsAB operon. The mmsAB operon contains two structural genes involved in valine metabolism: mmsA which encodes methylmalonate-semialdehyde dehydrogenase, and mmsB which encodes 3-hydroxyisobutyrate dehydrogenase. The cupin domain of members of this subfamily does not contain a metal binding site.	4.76023e-30
NZ_CP009280.1\|WP_042134098.1\|1430164_1430725_-\|adenylyl-sulfate-kinase	gnl\|CDD\|223603	COG0529, CysC, Adenylylsulfate kinase and related kinases [Inorganic ion transport and metabolism].	1.53817e-88
NZ_CP009280.1\|WP_042134083.1\|1417174_1418083_-\|aldo/keto-reductase	gnl\|CDD\|381312	cd19086, AKR_AKR11C1, AKR11C family of aldo-keto reductase (AKR). Bacillus subtilis uncharacterized oxidoreductase YqkF is a founding member of aldo-keto reductase family 11 member C1 (AKR11C1). It may function as oxidoreductase. This family also includes Bacillus halodurans AKR11C1, an NADPH-dependent 4-hydroxy-2,3-trans-nonenal reductase.	5.76958e-102
NZ_CP009280.1\|WP_042134087.1\|1420483_1420795_-\|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl\|CDD\|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	3.16815e-22
NZ_CP009280.1\|WP_081969839.1\|1407661_1409074_+\|Zn-dependent-hydrolase	gnl\|CDD\|236456	PRK09290, PRK09290, allantoate amidohydrolase; Reviewed.	1.50854e-148
NZ_CP009280.1\|WP_039302045.1\|1423822_1424623_-\|kinase/pyrophosphorylase	gnl\|CDD\|377080	pfam03618, Kinase-PPPase, Kinase/pyrophosphorylase. This family of regulatory proteins has ADP-dependent kinase and inorganic phosphate-dependent pyrophosphorylase activity.	7.21347e-129

>NZ_CP009280.1|WP_042134085.1|1419387_1420233_-|AraC-family-transcriptional-regulator
MAIFKYNSHRPHRTSPDLHLHYWGQEQCAPGHSVGPGVRDLYKIHFIHEGTGKVVVGEASHTLGAGQAFLTYPHVVTHYAADQDSPWTYSWIAFTGEEAGYLLSRTSLSPEQPVFPMDQELMPSLFERLSEAADCQDVLDLPLKVILYEFLSLLLRTVPATANLVIPRQKSVYVEQCLHYLHAHYCENVTVESMSASLKLDRKYLSTLFKRTIGLPPQQYLLNFRIAKACELLTETSCTIGEISHSVGYQDALLFSRMFKKVKGCSPKEYRIRHTDTDIVL
>NZ_CP009280.1|WP_039302057.1|1418238_1419228_-|glyceraldehyde-3-phosphate-reductase
MYIASPERYDTMKYNRTGRSGLLLPAISLGLWHNFGGNDVFENGRAMVRRAFDLGITHFDLANNYGPPAGSAEESFGQILKKDLAAYRDELIISSKAGYYMWPGPYGEWGSKKNLVSSLDQSLKRLGLDYVDIYYHHRPDPNTPLEETMSALDLLVRQGKALYVGISNYKPEEAREAAQILRRLGTPCLIHQPNYSMMSRWIEDGLQDVLAEEGIGTIAFSPLQKGILTDRYLKGITADSRAAGPSVFLSEKEITAEVIAKVSKLNDIAAARGQKMSQLALSWVLRGGKVTSALIGASKVSQIEDAVASLNAPELSAEELEQIENILRG
>NZ_CP009280.1|WP_042134083.1|1417174_1418083_-|aldo/keto-reductase
MNTNRLGQSDLYVSAMGLGCMTLGTDEVKAAAIIHEALDHGINFLDTADLYDEGRNEEIVGQAIRHRRADVILATKVGNRRIPGQEGWSWDASKSYIRSAVKESLRRLQTDYIDLYQLHGGTLEDEIDETIEAFEELKQEGVIRHYGISSIRPNVIREYVQRSGIVSVMSQYSILDRRPEESILPLLAREGISLIARGPLASGTLTEHGRSKAERAYLDYTAAELSELHGQLMQQTTLTRTLTQTALQYPLADPAVAAIIPGASSLAQLRQNIASATSPPLSALELETVRKVSKAGRYTVHL
>NZ_CP009280.1|WP_042134081.1|1416761_1417055_+|hypothetical-protein
MDRLTWEALLTFVLLVAGFISLYAAIHKRTNFARYSMTVLLIASGAPLAVMLVLESRRDALDANIGLGMAFLLTWLITALVFAASVIIWIVKKRKHG
>NZ_CP009280.1|WP_042132671.1|1415260_1416553_+|group-II-intron-reverse-transcriptase/maturase
MNAKRLTTPKEKVQELQEKLGQAAKENSKRKFHALYDKVYRWDVLCEAWKRVKANKGAAGVDEVTLADIVEQGETRFLKECERALKEGNYHPQPVRRHYIPKKDGKPRPLGIPTVRDRVVQMATKLVIEPIFEADFEDVSFGFRPKRSAKGALDRIRKACNRKGNWVVDVDIQGYFDNINQEKLMKLVQMRINDRRILKVIRKWLQAGVMEEGNVRRSDLGTPQGGVISPLLANIYLNYFDRLWEKHGSGLGELTRYADDFVVVCKSKKDAEHAYELIGRIMERLELTLHPTKTRIVGLWTGDEGFDFLGMHHRKTKAETSQGKVYYTTQQWLTKKAEERIRGVVKERLAPPSMRSRSFVEHVEWLNPKIQGWRNYYYTNYSQKRLAKLDWYILQRFTRWYAKKRQRGRWMSSVSEVKYSAKQYGLKTLL
>NZ_CP009280.1|WP_081970421.1|1414523_1414667_+|S-layer-homology-domain-containing-protein
MCSITAWARPYASAARKLGLILGQGGNKFNPLQKATRAEAVQLISKL
>NZ_CP009280.1|WP_081969841.1|1413785_1414520_+|ZIP-family-metal-transporter
MASAFLGSFLSAMATVLGVIPILFVKRLSELWKDVLVAFTAGIMVSATTFGLMPQAIKESGIIALTLGLITGVLLLDLIESHIPHIDVENKPGLSNLDSKALLVMIALFIHNIPEGLSTGFSYASEQASLGPMVAIAIGAQNMPEGLILAIFLMNARATRRKALTIAALTGLMEMVSAVIGYFTASYVQNVVGYGLAFAAGAMLFIVYKELIPESHGHGYERPSTYSFIFGLLAMVYITTFFGG
>NZ_CP009280.1|WP_156118543.1|1410567_1413429_-|hypothetical-protein
MNLMSLGQSFAASSAHDTSGATVVGKDAAGHWAEGVLTEWQQQGLLTGYQDGSLQPDHQITRAEFTALINKSFGYTNTAAITYADVKSSSWFYTDITKAAAAGYIMGYPDQTFRPNQSLSREEMAVIVSSVLKLNAVDMAASFTDTAAGHEWSKKQINAIAAAGLMNGYGQKFRPLATATRAEAVSVLDRALKLQTSSSANTIVYDKAGNYGPETGVVTVNGSVYIEASEVVLSNTIITGDLVISEAVGKGDVTLKNVTVKGTTTIAGGGKNSIHVVDSVLVTVIVNKKDGSIRIVTEGTSSVEQITLQSGALLEEGSGTGSGFGNIDLSAAIPASAEVALAGTFETVDIFATAIKVNLTSGSIGQLTLAPGAANTRIDIASGASINTLILNAVASVTGKGSIGTALINASGSTIAQTPGHVSYGNNASAVVGAPVVSGNSSNSHAVTEVVYGFEGYISDVDNHPVADMTIHFRKGLAATTGTIAASVITDAEGKYFANLAPGIYTGELSKAGYITTYVIGASLTTHKNTEQNATAIKIPAADEIRIVLTWGEYPYDEDSHLIGPAPGNQSFHTWYGDREFSNNDVVYADLDHDDTSSYGPETTTIRKRVDGKYTFYVHNFSGNGADHTQTLAASGAKVEIYNGSNATPVKTYHIPVADSTDEYWHVFDMNVAGSELSFTDTNMLTVNPPYVEVDVSPTPNTYNLSVENHVGTNDIVNVYGLEPGDVISVYSEEGGTAEPLQTATVYGESTSIRMTGLDFGKEYTTIYISLKKPNRTESYAIPIPVLSEASYAELATTIAGNFKDRVLPGTMTVGQTVYMADPAFEWPRDFDVRIMDFQAPSTVTDDVYLLRDYYLWYMDYNGTAEPVKYSITLELKLDSSAVTKEIFITVPSVFTALPETIAYARTLNDDRLADPLTAAEVVVSNPEATAEQYIQAIKDLHWIFSLIANEEE
>NZ_CP009280.1|WP_042134079.1|1409086_1410403_+|amidohydrolase
MREIYSADVLYTQDEFKKNGALLVENGIITDVGEREELLGRYPDARHIHWENRAIVPGTVNSHNHSFQSLLRGIAIDKPFLDWRDQALYKYTPLLDEEAIYTGALLAFGEMLRYGITTVCDFFYVHNGGTVYDEAVIRAAGDLGIRLVFARTMYDWTGAPLAYRETVPEAVERTRSLAKKYQGNPMVTVHPAPHSPHAASPEMIKAGHKLAMELDTPFHIHVAEEMFEVEEIQRDYGLRPVYYLDSLGVLDERMIAVHLVWVEDSEIELIGARRGSLAYCPSSNMFLADGVTRIPDLLKAGVRVTLGTDGGCSNNRISVYEEMRMCALLQKVSRLDGTCITAGQVYRMGTRSAGEILQLPVGSLETGQHADFAALDLQDLSLAPKRELFANMVYAMQPGAIRTVVVGGKVVFEQGKIKAVSEAAIGGRVDRLFEKWAK
>NZ_CP009280.1|WP_081969839.1|1407661_1409074_+|Zn-dependent-hydrolase
MRALRINAERLQNNIRELAKFGLNEQTGGLDRTTFTEAELAARQWLKSKLLDLQLRVRVDEAANIWATRRGTGQGTISGDSDVMECPEAPEDLEVSGVPDGQRISDPSGNSVAAGGSCASGRARESLPVIAFGSHIDTVPNGGKYDGALGVLLALEVMTVLEENKINTRHPLELVSFSAEEPNPFGLSTFGSRAVSGKLRQDDLAGVRNDQGQLLTEALRRAGGDPEHFEQCRRDPEALAAFLEVHIEQGKRLLDRGIPVGIVTAITGIYREEITVTGEANHAGTTLMQDRKDALMGASEMMLAFEAVCRKQPADEAVGTIGRISNEPNAANIIPEKVLFHLEARGADRQQIQEMIGDWSQQAEGIARSRALRLERRLILDQAPQPMDARVIDVSAAQAEALGIPVLQLGSMAGHDATHMASLTCAGMLFVPSLGGKSHCPEEESRIADIEKAGNVLLQSILALDEQLSR
>NZ_CP009280.1|WP_042134087.1|1420483_1420795_-|(2Fe-2S)-ferredoxin-domain-containing-protein
MNMRLKVLKKHLLFCCSEHCNNQDVEEVMQEFKEQMVEHGINKTVKINKTSCLGLCGNGPFVIVYPDGIWYYNVTTDDVARIVEEHLVNGVPVEELVMLKMEA
>NZ_CP009280.1|WP_042134089.1|1421168_1422347_+|YsnF/AvaK-domain-containing-protein
MNKKIVGVFYTEHEASRAIEDLKSHGFLTEDISVIARNKRDVEAISDETGTKAPEGMASGAATGGILGGVTGLLAGIGALAIPGIGPIIAAGPIAATLTGVAVGAGTGGLVGGLIGLGIPEDEAESYDNYVDEGRILVMVDADNTRESDVYSIFRNHNSANADRYMDDPNTTGDAADTARHSVTDTVDAAFNGSGLEGRDDTGLDTMNSATEHDLPGTRALDDVNRPGMTGDVYSGTPNGIDGALDSTRTGGFNDPDEDRRLRLREEQLDVSKNKVQTGEVNVHKEIIEEQKTINVPVTHEEIVIERRAVNNDTTAEPVGADETIRIPVSEEQVEVRKNTVVTGEVEIHKREVQGTEQVQDTVRREEARVDKSGEVKVDGSDELLRDHSRSR
>NZ_CP009280.1|WP_042134091.1|1422792_1423788_-|class-II-fructose-bisphosphatase
MERELALEIVRVTELGALSSARWIGRGDKNAADNAATTAIRSMFDSVSIDGTVVIGEGEMDEAPMLYIGERVGNRNGPSVDVAVDPLEGTEVVACGLHNAQSVIAIADKGSLLHAPDIYMEKLACGPELAGKLSLDDPAEVTLRKAGMITGKALSELTVMVLDRKRHEGLISILREAGVRIKLINHGDVAGAIAAALPDSDVDLYMGSGGAPEGVLAAAALRCLGGELQGRLLPEGPFEMQRCLQMGLDNPARVLSMEDMVGTGDVIFAATGVTSGEFLSGVRFIGKERAETHSVIMRAQSRTIRYIRSIHFLPGKDIPEVIPARANAAFM
>NZ_CP009280.1|WP_039302045.1|1423822_1424623_-|kinase/pyrophosphorylase
MEPSTHYITICSDSIGDTAEAVVQAVIHQFQNQRVTIRRYGNVRHEDELRKLMEETAQLQGFVAYTLVQPELREMIREEAVRLDLRIVDIMGPMMQAFIDTFDDAPEARPGLLHQLDEEYFSRIEAIEFTVACDDGRDLGAMLKADIVLLGMSRTSKTPLSIFLAHRGKKVVNYPVVPEVGPPQQLLSLPPNRIIGLTMKPEYMLKIRSERLKMLGLPTGSQYASLERITEEMEYAATLFAKLGCPVIDITDKAIEETAGIIMGYI
>NZ_CP009280.1|WP_042140795.1|1424641_1425262_-|helix-turn-helix-transcriptional-regulator
MQIIEIVKKRAPITGDQIAESLGLSRPTIRGDLSILVMLEYVDAKPKVGYFPGTKAAARHNSRGLLQDTKVSDIQSIPVIIRENTTIQDAVVTLFLQDVGTLIICDSDGKLTGVASRKDFLKVTLGNPGAVTMPVSMVMTRQPKVITVSPDDTVLDAAQRMIYHEVDSLPVVVPGSGEGSGSGLDVVGRLTKTSIVKLLLELEAKG
>NZ_CP009280.1|WP_042134094.1|1425600_1426194_+|hypothetical-protein
MRKSSFVLICGIVILTLLSAGCSKDTPKYAELFTQVEEHRAVFNQPLEDGLAVLGVTDAVGEYDPNLGTIMQDDVLTVNQMEFIQQITADVTNDTIIGYRIGTVFPRSESGYEDARELVRAFLEHYKPADDEEADKVEQSVQTIDRMALPLMPSIGFIRESWTYGEGEKKLYITYRISNSFESDEELPLNLFFSSEE
>NZ_CP009280.1|WP_039302038.1|1426297_1427248_-|EamA-family-transporter
MIMLAYSLVCLIFGTTFLAIKIGVDAGAPPFFSAGLRFFTAGAVLFLFMVVKGKASFSLLLRKEMLFTGATLTFGTFAALYWAEQYVSSGLAAVLSATGPMMILLMQMAFLRQKAPAYSLFGCIIGFTGVLLLVLPSLAADVTPLWLIGCVVVLIGEICYAAGAIYSKKVTTTFSGVSPVALNAAQMMYGGALLFIISLFTEPLHPAFLLSFKTAGSLLYLTVVGSMVGHTLFYWLVSKTNPVFPSTWLYISPPIAVGVGFLFYNEAVTWVTLLGVFTIIAGTVLVNAGALKQLIFKQKPAIPVLQKTSIEALPQD
>NZ_CP009280.1|WP_042134096.1|1427489_1428926_+|PLP-dependent-aminotransferase-family-protein
MKKSVGAEQSNPLFRQVYEFMANRIGRGEWKPHDKLPSIRLLADELGVHRLTVFKAYRALTENGMLYVKDKSGYYVSPGSRMANSVEEGAAVLGYTVKSPMSDIQRKPVTYQFSQALIDPGLLPNLFLSDYVKKVFDLYPKVMGTYSTVQGDEELRATLSSHFHDRYRLQLSASELLITSGAQQAINLIAGIMLGPMDAVLVERPTYSVALDIFRRAGARLVPVEISPQGYDLAAVEELMRRHKPRMFYINPTHHNPTGYTVPAKQRKLLVELAERYRCLLVEDDPFRDMHFEEEPPAPFFAYDTEGWVIYISSFSKYVAPGLRICAVACRYPFMERLIAAKSLADNGTPLLNQKIFLHYYTSPRLQQHLGKLRIALQVHKEIMEEELAAAGWEWTAPQGGLNLWVKLPDTVSVDVLFVRCMEQSISFVPGEICDPLGEMKSWLRLSYSFASEALLREGMRQLTAIAREIEAEGEHRE
>NZ_CP009280.1|WP_052421691.1|1429286_1429958_+|hypothetical-protein
MMIAIKRIRGVLLMFLCALLVFMTLLTVRPQVTYACSCVIPAPPLEAMENSTAVFEGTVISVAKPSGIIQSSADPMQVTFQVGARWKGDLGNQVTVSTAQSGDSCGFEFAEGERYMVYARGAEADGNLAKGNEEQSELTTSLCSRTALYADAQEDLNELGPGTGGGSPTAPPETAEGDAPSVPVDNHSATAPWLLYVGAGAGMVILIALGLTWQRRQSNKSRK
>NZ_CP009280.1|WP_042134098.1|1430164_1430725_-|adenylyl-sulfate-kinase
MTAQLHAQTQTGVTIWLTGLSGAGKSTLAALLKDRLQEQGRAVEWLDGDELRRTLGRGLGFSREDRFENIRRAVYIAGLLNRHGVVTVVSVISPYADMRSYARRELPGFVEVYVDCPLPVCEARDVKGLYAKARSGEIPAFTGISDPYEAPDRPELRLLTAERTPEECVEEMIDWLTENRLYQPWR

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_CP009280_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_4

2115415-2115507

Orphan

Consensus_repeat	Method
CTGGAGAGGAAGCAGAAGCACAAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_4

>merge|NZ_CP009280|4|2115415-2115507|CRISPRCasFinder
CTGGAGAGGAAGCAGAAGCACAAGTGACGGCGGTGCTGAAAAAGGAAACGGGGCGGGAAGCAGCAGTATCTGGAGAGGAAGCAGAAGCGCAAG

>NZ_CP009280|4|4|2115415-2115507|CRISPRCasFinder
CTGGAGAGGAAGCAGAAGCACAAG	TGACGGCGGTGCTGAAAAAGGAAACGGGGCGGGAAGCAGCAGTAT
CTGGAGAGGAAGCAGAAGCGCAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_052421731.1\|2120773_2123473_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042134912.1\|2129676_2129991_+\|multidrug-efflux-SMR-transporter	unknown	unknown	gnl\|CDD\|224987
NZ_CP009280.1\|WP_042134903.1\|2112865_2114545_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270299
NZ_CP009280.1\|WP_042134897.1\|2102162_2102663_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224759
NZ_CP009280.1\|WP_042134895.1\|2100321_2101956_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP009280.1\|WP_042134899.1\|2107599_2109891_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042134894.1\|2099755_2100223_+\|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224759
NZ_CP009280.1\|WP_063779786.1\|2125671_2127786_+\|nucleotide-pyrophosphatase	unknown	unknown	gnl\|CDD\|225914
NZ_CP009280.1\|WP_042134908.1\|2124533_2125391_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|227311
NZ_CP009280.1\|WP_052421728.1\|2103388_2107342_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|269893
NZ_CP009280.1\|WP_042134905.1\|2117935_2120275_+\|glycoside-hydrolase-family-95-protein	unknown	unknown	gnl\|CDD\|379625
NZ_CP009280.1\|WP_042134901.1\|2111865_2112771_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_039307795.1\|2110965_2111850_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_CP009280.1\|WP_039309990.1\|2098664_2099120_-\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|341362
NZ_CP009280.1\|WP_081970440.1\|2129215_2129677_+\|multidrug-efflux-SMR-transporter	unknown	unknown	gnl\|CDD\|224987
NZ_CP009280.1\|WP_052421730.1\|2116053_2117874_+\|alpha-galactosidase	unknown	unknown	gnl\|CDD\|379079
NZ_CP009280.1\|WP_052421732.1\|2127788_2128133_+\|thioredoxin-family-protein	unknown	unknown	gnl\|CDD\|239245
NZ_CP009280.1\|WP_042134906.1\|2123771_2124500_+\|thioredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|372611
NZ_CP009280.1\|WP_042134910.1\|2128242_2129151_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP009280.1\|WP_042134892.1\|2099238_2099673_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042134912.1\|2129676_2129991_+\|multidrug-efflux-SMR-transporter	gnl\|CDD\|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	8.81886e-28
NZ_CP009280.1\|WP_042134903.1\|2112865_2114545_+\|extracellular-solute-binding-protein	gnl\|CDD\|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.22938e-164
NZ_CP009280.1\|WP_042134897.1\|2102162_2102663_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|224759	COG1846, MarR, Transcriptional regulators [Transcription].	2.37388e-11
NZ_CP009280.1\|WP_042134895.1\|2100321_2101956_-\|MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.7392e-59
NZ_CP009280.1\|WP_042134899.1\|2107599_2109891_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	9.60114e-24
NZ_CP009280.1\|WP_042134894.1\|2099755_2100223_+\|winged-helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.30146e-15
NZ_CP009280.1\|WP_063779786.1\|2125671_2127786_+\|nucleotide-pyrophosphatase	gnl\|CDD\|225914	COG3379, COG3379, Uncharacterized conserved protein [Function unknown].	5.39129e-19
NZ_CP009280.1\|WP_042134908.1\|2124533_2125391_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|227311	COG4977, COG4977, Transcriptional regulator containing an amidase domain and an AraC-type DNA-binding HTH domain [Transcription].	2.78929e-22
NZ_CP009280.1\|WP_052421728.1\|2103388_2107342_+\|hypothetical-protein	gnl\|CDD\|269893	cd14792, GH27, glycosyl hydrolase family 27 (GH27). GH27 enzymes occur in eukaryotes, prokaryotes, and archaea with a wide range of hydrolytic activities, including alpha-glucosidase (glucoamylase and sucrase-isomaltase), alpha-N-acetylgalactosaminidase, and 3-alpha-isomalto-dextranase. All GH27 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. GH27 members are retaining enzymes that cleave their substrates via an acid/base-catalyzed, double-displacement mechanism involving a covalent glycosyl-enzyme intermediate. Two aspartic acid residues have been identified as the catalytic nucleophile and the acid/base, respectively.	2.45931e-88
NZ_CP009280.1\|WP_042134905.1\|2117935_2120275_+\|glycoside-hydrolase-family-95-protein	gnl\|CDD\|379625	pfam14498, Glyco_hyd_65N_2, Glycosyl hydrolase family 65, N-terminal domain. This domain represents a domain found to the N-terminus of the glycosyl hydrolase 65 family catalytic domain.	5.66694e-47
NZ_CP009280.1\|WP_042134901.1\|2111865_2112771_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.85695e-60
NZ_CP009280.1\|WP_039307795.1\|2110965_2111850_+\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.21324e-115
NZ_CP009280.1\|WP_039309990.1\|2098664_2099120_-\|CBS-domain-containing-protein	gnl\|CDD\|341362	cd04586, CBS_pair_BON_assoc, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the BON (bacterial OsmY and nodulation domain) domain. This cd contains two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the BON (bacterial OsmY and nodulation domain) domain. BON is a putative phospholipid-binding domain found in a family of osmotic shock protection proteins. It is also found in some secretins and a group of potential haemolysins. Its likely function is attachment to phospholipid membranes. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	2.90883e-32
NZ_CP009280.1\|WP_081970440.1\|2129215_2129677_+\|multidrug-efflux-SMR-transporter	gnl\|CDD\|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	4.9588e-33
NZ_CP009280.1\|WP_052421730.1\|2116053_2117874_+\|alpha-galactosidase	gnl\|CDD\|379079	pfam13229, Beta_helix, Right handed beta helix region. This region contains a parallel beta helix region that shares some similarity with Pectate lyases.	0.000245234
NZ_CP009280.1\|WP_052421732.1\|2127788_2128133_+\|thioredoxin-family-protein	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	1.10567e-14
NZ_CP009280.1\|WP_042134906.1\|2123771_2124500_+\|thioredoxin-domain-containing-protein	gnl\|CDD\|372611	pfam13462, Thioredoxin_4, Thioredoxin.	8.00274e-34
NZ_CP009280.1\|WP_042134910.1\|2128242_2129151_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	1.05691e-46
NZ_CP009280.1\|WP_042134892.1\|2099238_2099673_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	9.39497e-16

>NZ_CP009280.1|WP_042134903.1|2112865_2114545_+|extracellular-solute-binding-protein
MKKSLISLLMLVTVLTVVISGCSGKNTDSPSGAQATSGNASGNTPAAAAPVEVSVFAVQESGIDIPTNKFTTFLQDKFNIKFDWQINPSDGAKEKRQISLASGDYPDAYLLTAYIDEFSQGDVLKYGQQGVLVPLNDLIDKYAPNIKAAMEKTPALKTLNTAPDGNIYGLGAYTECFHCSYPNKMWINTEWLKKLNLEEPKTTEEFKQMLEAFKTQDPNGNGKADEVPLSGSTEDFGVRIIPYLMNSFVYDDDRNYLNLTPDGKVESAAIKPEWKEGLTYIKSLFDAGLIDPGAFTQNAEAFKKIGENADAEILGAGAGMHPAIFINIDPGNTRSAHYNPLAPLTGPSGVSFATHDAGGVSPGAKFVITNKASEEAQIALIKMVDYMFTPEGQTNSASGMKGIDWTDPGEGDVALGKDSKPVIKQIPMAEGEAPRNAGWSGMGHFYMPKEYRDTFVQGTDIYASNGYERRLYDATLLYEGHEPKDLFPLWSIWIDPSDIDEASMLQTNLRNYIEQNELQFITGNKDLNKDWDAYVKGLKDLKLDRYLEILQKAYDVSAK
>NZ_CP009280.1|WP_042134901.1|2111865_2112771_+|carbohydrate-ABC-transporter-permease
MAASAAVSQKIKESTGDRIFLTVVYAVLILVVIAVLYPLIFIISSSISSPAAVTSGRVWLWPVDISFKAFKVLFSTHEIVSGYANSIFYTAAGTLISVTLTVMIAYPLSRKAFFGRNALMMVITFTMIFSGGLIPTYMVVRQMHLIDTRWALLIPNAIWVWQVIIARSFFQASIPEELLEASEIDGCSDMRFIRSVVLPLSKPILAVLVLMYAVGQWNSYFDALIYLKTADLFPLQLVLRSIIIQNNSSGAMDAMAMVERQQMAELLKYALIVVATLPVLVIYPFVQRYFVQGMLVGSVKG
>NZ_CP009280.1|WP_039307795.1|2110965_2111850_+|sugar-ABC-transporter-permease
MLKHWQLHLLVIPPLLFFLIFKYYPMANAVLAFKDYNVIKGIWGSPWVGFRNFELFFENPMFWTLVKNTILLSGFLLLAGFPIPILLALMINEIRGGRFKRFVQLVSFAPYFISTVVMVSIIMLFLAPRLGFANIALNFFGLESVNFLGEPGMFRSIYVWSDIWQTAGYSAVIYLAALAGIDPTLYEAAKVDGASRFQKIRHIDLPGIVPTIVIILILNVGNVMAIGFEKVYLLQNPLNIVNSEIIATYVYRIGLLNANYSFATAVGLFNSLINLVLLLTVNGLAKRITNNSIW
>NZ_CP009280.1|WP_042134899.1|2107599_2109891_+|helix-turn-helix-transcriptional-regulator
MPKYSKVFRRFLISYLVILIIPSIGGYMSYHTSISVTQSISIENSVTQLEKSQEILERRMAEVEGLTRQLAINQELNVLMNEQGRETNVFGIWRAMRNVLTFGQTNDFLQDYYIYLANYDLVLTAGSSYRPDHYYEIYHYKDLPLEEWKKEILDRTHRSEIKPLSAFVSKGTPTSVITYMQSLPLDSFNNSSPAVVVVNIDEKIIASLLSGLTERDGGWVHISDADGNTIVLQGQNNAYVDKLAADPFFDADKVSQFYRDDLVITTRSGTNGWVYQAGIPRSVLMENANKIKHMTWLITAGALFLGLLAGLVLAYRNSMPINRLLAVMKEQFGKEDSPERNEFDFLSGNIADMITKNKLLETELNRQLPLVRDAFLKRLIAGEFESREEIVSAAEQADIGLGEGTGYAGILQIKGYTGMDSVEILNELNAARLLLKQTFAELAGPLPMTDMGSDKIVILFFSSTADGGPAGNEDGMERLMDQGVQRVFEEYRISVQGGFGEYFSSVTEVSQSFEQARQALEYAVYTNRKGVLRHQEVQIENTTYYYPLETEQRLISTIRAGELAEAERIMEATFAQNLGPRELSMEMKHQLIGEMKGTFLKLLDQKIFMESPLGESVKRQIIDIDTSAPLERIQTEFLELTGELCGFITNKKKDAHTQIIKQMYQYTAEMYADTELTLYRVAEHVERPEKYISQLFKEVTGVNYSDHLIKVRMDEAAILLRESRYTVDEIAARVGYNSSHSFRRAFKRLTGISPSTYRQSHGE
>NZ_CP009280.1|WP_052421728.1|2103388_2107342_+|hypothetical-protein
MKSLGKKIGLCLLMLIMTAAQTGLAGTRQNVAEAADKELAQKPYMGWSSFSMQVYEPSGNWISADSIKKQSDAMHEKLQSHGYEYINIDAGWNGSMDEYGRPIPSTERYPNGFQEVIDYVHNNEQKIGIYLIPGLSIDAYNQNLEIYGTAGECRMQDIAVQPLKIVDAWNAYSYKIDFSNPCAQKYIDSIADMLGEWGIDFVKFDSVTPGSGINNLSLDARGDVEAWSKALARHDIWFELSWALDHNYVDFWKKYANGWRIQWDVEAYDSNVGLTQWANIARLFPDAALWWRDAGPGGWNDFDSLNVGNGAMDGLTKDERQTAMTFWAVSAAQLYIGNDMTRLDDYGLQLLTNDEVIAVNQSGRPAHPVSMDTKQQVWYANNGDGTYNVALFNLGSRSAAVDVKWSDIGLEGPASVRDLWSHTELGTFEDGYSAGALEPHASRMFKVTAKEGTSIVNDDDTGLRYTGSWQRNGGKEQVPGSQDMNISITDTSPAPGEGDPGDGGQQGGGAGADPIDPGTGSGASVTRSVYVNDSNPAIAYSGSWSSSTGRSAGDHRADVHYTEQNGDYFQYTFSGTGIELLTEKDPAQGDILVYLDDATSPDRVSTYTSGDKEAQQIVYSASGLAEGEHTLKVVKDSGQYMLLDALRITAGQLINPQAGSFDKAPGSQADLELALAAGSDSLLAITNNGVALLPGADYTADGSTVILKKEYLFNQPSGLTELALSFDGGSSELFTVQITGSSTVRYEQINNDDPGITYNGSWSRSTGRNMGDYKDDVQYTELNGDSFEYAFNGTGISLYTEVDSSQGDMDIYVDGEFKETVSAYRNGRLAQQNLYSISGLPEGIHTLRAVKKSGRFMLLDMLKVEIPDLVNPVEAVFDKAAAAQADIDVTLLRQPGLFGGIRQGSYTLVEDTDYTLSGSTVTLAKSYLAAQPAGTLTLIFEFSGDYQNDVHYTEKDGDYFEYAFTGSGISLVGPTGPELGDIELYVDGELRQTASAYSANRQILQSIAVITGLEAGPHVLKAVKKSGGLMLADQVRITLPAADEGPGEEPTATPAPSATPEPAATPEATATPQPGATAQTGGNPAPAATASPAVTVAPSPTSAPVPSSTPGIAEEHHSAYAKGYPDGLFKPNQKITRAEMASLLFAAITPEAGGTAASFSDVSADYWAAAAISAVAEAGVMTGYSDGSFRPGQLITRAEMASLAAVLIPADTAYTAAGRGFPDIAGHWAEAAILKAQGAGILSGYSDGSFKPGNPLTRAEAVTVINRLTGRGPLRGMAVTSWRDVPLTHWAYADIMEASVNHAWKPADGGGEQFSGS
>NZ_CP009280.1|WP_042134897.1|2102162_2102663_+|MarR-family-transcriptional-regulator
MSIQDSQERQLLITLENIKRLTPRQQSMDSIPHGEFVTMFVIHAAMKQQEADQQERGGPCRGLMVSRLSELMQVSRPTASQMVSTLEEKGYIERVMSETDRRVIYICLTAKGQAVFGSRMDRYSDVLAEIIDKVGREEIDQLISTCGRLMEAVNEVRPRVMGNASE
>NZ_CP009280.1|WP_042134895.1|2100321_2101956_-|MFS-transporter
MEHLTQKKKVTIMIALMAAMFFAAINQTIVGTAMPRIIAILGGIEHYTWVITIYMLTSTIATVLVGKLSDIYGRKPFLLAGIVIFIIGAFLSGLSDNIYQMITYRGIQGVGGGILMSATVTAVGDLFAPRERAKWTGIMMAMFGFSSVIGPTLGGFMVDHMDWRWIFWIFLPLGIVAFIMIWRMFPKGTRAASETIDYPGSIFLSLSIVALLLGFSWAGTKYAWSSPEILGLFAAAIAGAVILILIERKAKSPVLPLSLFKNSIVTISMIIGFLMNAGMMGAMIYLPFFVQGVEGVSPTNSGFINMPMSLMMIVLSTLAGRWISKSGKYKRYAMIGMPFMVAAMIMMAFMNSIIMAVASMIVFGIGLGLAMPVFTLTVQNAVAPQMLGVATATTTLFRNLGGTIGIAVMGTVMNTTLTHKLESAVASGKGPDLSKLDPEAAGQLTAFMNPQLLLDQPKLKELHTTLPEQIRPLFNQLIEMLRGALSDSLTVVFLSGTALLVIAAVLVLFLKEIPLRSSESKTEAAAEEAGAGSKLRKETAPAGH
>NZ_CP009280.1|WP_042134894.1|2099755_2100223_+|winged-helix-turn-helix-transcriptional-regulator
MNEDKYEHIDDLIEAFQQFARMNWRKTTLWGLKPSEIRVLVSIKKGMEQEGNKGRTVSDISKLLKVTSPTVTQMVNSLIAQGYAVRTPDSQDRRISDITLTDKGAHLADMAVAKSRETFQGMIDHLGKERSETLSELLNGVYEYFEQLNSQQNDF
>NZ_CP009280.1|WP_042134892.1|2099238_2099673_+|MarR-family-transcriptional-regulator
MEKRSIETIELEMAVLVRRLTSLTTYKKIGNLDRAAYLLLHQIAFNNGTAGVKMLSDEFQLDISTVSRQAAALENKGYIIRVPDPVDGRAYTLQITELGGEILDENRQMRQEIMGKLLANWSDEEGDSFGELLRKFNATFLEED
>NZ_CP009280.1|WP_039309990.1|2098664_2099120_-|CBS-domain-containing-protein
MKAHEFMIRQVYKVKQEDTVRTFIEKCITHRISGMPVVNDRNEIVAYLSDGDIMRYIGRHEDLIVDSFFQINVFVGDNDEFEERTRKLLNLNVMAIAKKKVVTVHYEEDIEQIATILGKKQIKKVPVERNRVLVGIISRGDVIRHSFKALL
>NZ_CP009280.1|WP_052421730.1|2116053_2117874_+|alpha-galactosidase
MFDIHHEVHPVDDDQPVHRTVLCLTDFGAVPDSDGDTQPAMRRAIEAAGRLEGPVLLDCPQGCYHFYPDAALRVPYYITNTASEEELPDVTKTAGLLLKGQRQLTLDGNGSLFLFHGKQTMLILDGCTDMEIRNLHLDYVQPTVAEMTVEQCGADFCEVTVHSDSRYELIGGRLDWIGEGWRFRGGPMQVYDPVQNITWRTDNWLAEARLVEVIGPHSLRFSFGFRPDVAPGTVLQVRDGIRDQAGIFITECSGVTFQNAGVHFMHGLGIVGQFSRDLVFRQLELSPRPETGRTVAGFADFIHLSGCRGQLLIEDSRFSGAHDDAINVHGTYLRIAGQPAGNTLKVRFMHPQSYGFMAFHTGDEIEFVRAESLTAYAVSRVAGVRQLNPRELELTLEGPVPPGIGGNDVIENVTWTPEVEIRGNVFSRIPTRGILAATRRRTVIRDNVFERMQMSAILVAADAESWYESGAVRDMTITGNTFIACGSSEAPVIHIAPEKKEADSGAPVHRNIRIEHNLFETGDTPVLSARSTEGLTFRHNRVVVAAADAGDRNRKMGKDKDKDTDKDKDKDKSMDEERFSSLENAVRLTACSGVDVTANSFCIEEQ
>NZ_CP009280.1|WP_042134905.1|2117935_2120275_+|glycoside-hydrolase-family-95-protein
MNDFKLWYSEPAVSWAQGLPLGNGRLGAVVMAAPHREVWSMSEVTYWSGQSDPVPSSGGGKAALEEMRQHFFSGDYEGGDRLAKRHLQPKKQNFGTNLGLCEVVIDFAEQMQNREQESGDGGQFRRELDLTNAVAGAVHQGKSSTLHREVFASHAGDLVASRIWGGLPGTVSFSLSLVNGTGQFRATAVEGDMLEFKSQATENIHSNGTCGVYAKGWVKVVISGGSIHSGDGLLTVSGADEAWIYFAVSTNYRRTDADWESESRSTIDQAAGKGYELLREEHIADYRSQYDKVNIHLGRSDKADLPTGQRIQSLARGGGDDPQLFALFLQYGRYLTIAGSRADSPLPMHLQGIWNDGEACRMGWSCDYHLDVNTQMNYYPTEITNLGDSHLPLMRYVEELAQAGKSTAGNLYGSKGWVAHVFSNVWGFTLPGWETSWGLNVTGGLWLATHLIQHYEYSLDREFLARQAYPVLKEAAVFFLDYMCIHPKHGWLVTGPANSPENSFYPGDPGDGAQQLSMGPAMDQILVRELFEFCLMAAALLDRDEAFRQMLQAAAAKLPPLQIGRKGQLQEWLEDYEEAQPEHRHLSHLFALYPGNRITPGRTPELSRAARVTLENRMQQNELEDVEFTAALFGLGFARLHDGEDAYKHISHLIGGLCFDNLFTYSKSGIAGAESNIFVIDGNFGGTALIAEMLLQSHAGEIHLLPALPAAWSTGAVSGLRAKGNAEVDVAWDNGQLTAAEVRTFSPGMVTVRWGEVRTVFQAEAGGSYKLGSRLELLA
>NZ_CP009280.1|WP_052421731.1|2120773_2123473_-|hypothetical-protein
MKKTKVSSVTEGAEEAKAEVETIEAEVMVELEMAGAVAAVTEMVEAVSSVMEADPMVVEETVEVIGAVTEMAEAVAATEPGPAAGYAAAGSLLHAQEQAGRHNITFSGPAVDFFEGALLGNGGLGVVVTTRPDAVMLHFGHNNVWDIRIAEHHGEEILTFKEVYDRFASLPADLGQLTDNPWYREYCEMAGDNYSKPYPRPMPCGSLLLRYDRRRAEVLGHTVHIGDGRCTVDFLINGKPAVFELFVEAEQDRVWMSVTDTATGSQVPLFHEARLIPDPKTPQEFPPASWENDAGAGLMSFTQILPHMEFPASPYLPHERDKAFRLAVRLPGAEFIGSGSIARLDSSGKSGGFLACAELREGPAAEIATLADTGTVIGAQPGPSASARMNAPTRAGYDHALAQTREAWREYWGHSFITLEDEFLEQIWYRNLYFLNCSVKAGITCPGLFANWSYGSIGADWHGDYHMNYNTQQPFWVTFSSNHLEKHLPYADMVDHVLPVSRKWAREYYRLPGAYFPHSAYPVEMSMMPYPVPHWGWEICETPWTVQSLWWHYLYSMDEEFLRSRAFMPMKEAVLFMTAYMKRPEAYGQPWKDGCYHIFPTVVPELYEITPGFARNSDCLIDLTLTKFIFRAFISACTVLGEIEAEGALLTEVQDILNHFPEYPEAESASGRVFVSVAGENPDTIYNVPVPLTTVFPGEEHGLHSPPAEYQTAVNTYRNHLNEGGNELVFQPLAGARLGILDLERFKRQIRYCLLPNGTCTNKVLMSGGRYSDTDDFSFMARMGIWFENFALPAVINECLLQSYNGVLRFFPNWPEHDSAEFRSLRAVGGFLVSASIRAGEVQQIEVFSEAGAPLSFYIPWEQGAECTRSSGEMQTFTGMAADMQTSAGEIIRIVKAGG
>NZ_CP009280.1|WP_042134906.1|2123771_2124500_+|thioredoxin-domain-containing-protein
MAKSKVKQTKKSSGFAVPVIVICVMVLAVSVAFLNRTRAAGGLDGLPNYTEIRGDFDANGLKYEKQPHLGSTTAKAKVIEFADFKCPACKKWKETYFEQFKQEFIDTGKVELFFINFAFIDRDSIMAASAGEAVFAQDNDKFWEFMSKLYDHQGDETKIWATPQFMLNFVKDNISGIDYERFAKDLQARTYMLPVKEDFKTAGNYGVNGTPKFMVNGQLLPGSSYEELAAAIEAAQASNVTE
>NZ_CP009280.1|WP_042134908.1|2124533_2125391_+|helix-turn-helix-domain-containing-protein
MNFSAIHPYVYLATRYPFAKGQSSSPRICYMSSVYLISEGYGTLLAGGQSHRVSPGMLIHLPPGKLHEWRADAAEPMVHLCCYFDWHLVDREGVFDWACPICYKPEQLKEELLGPLFPYPLPLSMDVGLLRGWTERFQKFYKAGEFDNEQTFIRNLTIQRHFQEFIDDLLHLLLSGQPIPDRRISSLLEQMEQDLLHDVPKPLEAYYSSLQLSRGHFFELFRKSTGASPVEYMNRFRVNRAKEDLLHSPLSITEIAEKYHFSSLHYFSRLFHRQTGQTPREFRTR
>NZ_CP009280.1|WP_063779786.1|2125671_2127786_+|nucleotide-pyrophosphatase
MANGKDGAHGSSNNSNNNNSKAKKVMLLGLDGADPAVIRKYVAEGKLPGFKRALDAGVTTSDLGMQSVLPAITPPNWASIATGAYPATHGITCFWNHTLGNELDVLDYGFDSGLLKAETIWQAYARAGKKSIIFNYPTSWPPQVEDAIYVDGTSIYTNLRGYIDYEKVYEGRAEYAELIEIPHVVDNTGANCRFEGEETSQKAEISKDTYEGYGYTQPGLVTTTQDGELSADVPTADQIYTPLRPAEGWTSAPAGAREFAVPVNNGQARRYGLLVADDQGDYSRVQIYASKTAAVPLGEAGPGEWSGWIYDTYSIEGADIPVAYKIRVLELDPAGNSFKFYASYVLDLKTGKYFYPQNIGEELYSKVGPMLQPSNYSRLNPQADQVLLESIEEMYSWHVDAINHLLDNNEWDLFYTHMHGIDMFNHFYLDHTLPAASAEYERYQEIIYKIYEISDRFISALLDRLDGGTAAFIVSDHAGVAKNPETDHPLIGDMWGINVGILGDLGYTQLKENGGSYEIDWSRTTAVAQRATFIYLNVKGRDPQGIVDPADYDSTVAKIIDDLYSYRDPKTGRRVISFALNRNDMEVVGLGGENSGDIFYILEADFTRCHGNGLSNHTLLGYSMRALFIALGAGVKSGEVIGRKVKVVDIVPTICHLTGSPVPENAEGGIIYQILAGSAEEEIPAAGKPAEAGEPVTAGAGGGV
>NZ_CP009280.1|WP_052421732.1|2127788_2128133_+|thioredoxin-family-protein
MRPEIPRRPVSHITDSEFEALAFGSEGPVLVFFGSRRCKICRQLFPVAEAIAHDFQGRMNVYGVDAGKYRLLFQSLRLRGIPQLVLFLDGEVKLRLGGYHPLPVLVEQLEQWVP
>NZ_CP009280.1|WP_042134910.1|2128242_2129151_+|LysR-family-transcriptional-regulator
MRLEQLYHIVAIAQTGSISTAAERSYISQPALSSSVSKLEVELGILLFKRTNQGVQPTDVGRAVIQKAMEAIDLLEDIKALAEENTQAMTGSIHLAVEPFISNTIMVNALTTFKYRHPGVNVLMKVGESNNNLRDIAAGKADFGVVMKTCGQPEEKDLCIKELFRDRLVLLVSKDSELAGRGAVPLQEALAQPLVLYNTEFATDCWVSELLQKHGDYNVAYRLDSFPMLENVIGQNLCAAFAPKFMSDYFLNKGSIVPLDIADTELDVSIVLAWTKRHHLSLMEKEMMETIKSFSSMLQFIG
>NZ_CP009280.1|WP_081970440.1|2129215_2129677_+|multidrug-efflux-SMR-transporter
MSAWFYVVAGGLVDIFWATGLKYSQGFRLFWPSLLVLCCIGISYTLYVKAMMRLPVGTAYTVFTGIGAAGTAAAGMLLLNEPAGFWRIFFILLLLCGMIGLRLTAGDESEAQEGGGEADAALRGGEPGRALKKGHFLPLSTTSPADREQGGLR
>NZ_CP009280.1|WP_042134912.1|2129676_2129991_+|multidrug-efflux-SMR-transporter
MGWLLLIIAGLSEVASVPLLKYSRGFRHLWPSVAAVAALALSFYCLSRSVMTIPVGTVYAVWTGIGSCGAVVLGAMVYRESLRPSKLICLAIIIIGMIGLRLTS

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_CP009280_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_6

2783552-2783781

Orphan

Consensus_repeat	Method
AAATCTTGTAAAAAGTACAACAATT	CRISPRCasFinder

4 spacers

The CRISPR arrays of NZ_CP009280_6

>merge|NZ_CP009280|6|2783552-2783781|CRISPRCasFinder
AAATGTTGCATAAAATACAACAATTCGCGGCGCGAATCGGCTAAATAAGGGGAATCTTGCACAAAATACAACATTTTGAAGCTCAGATCGGCTGATCAGCTTAAAATCTTGTAAAAAGTACAACAATTCGTGAATGCGACAGCCAAATGGAGGCAAATCTTGTAAAAAGTACAACAATTTCTGTATGCAGCCGCCAAATGGGCGAAAATCTTGCGAAAAGTACAACAATT

>NZ_CP009280|6|5|2783552-2783781|CRISPRCasFinder
AAATGTTGCATAAAATACAACAATT	CGCGGCGCGAATCGGCTAAATAAGGG
GAATCTTGCACAAAATACAACATTT	TGAAGCTCAGATCGGCTGATCAGCTTA
AAATCTTGTAAAAAGTACAACAATT	CGTGAATGCGACAGCCAAATGGAGGC
AAATCTTGTAAAAAGTACAACAATT	TCTGTATGCAGCCGCCAAATGGGCGA
AAATCTTGCGAAAAGTACAACAATT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042135579.1\|2785422_2785680_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042135585.1\|2788672_2789326_+\|deoxynucleoside-kinase	unknown	unknown	gnl\|CDD\|224345
NZ_CP009280.1\|WP_039303946.1\|2788052_2788676_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|224345
NZ_CP009280.1\|WP_156118588.1\|2795282_2803112_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP009280.1\|WP_042140990.1\|2781684_2782821_+\|carboxynorspermidine-decarboxylase	unknown	unknown	gnl\|CDD\|143502
NZ_CP009280.1\|WP_042135565.1\|2769452_2770892_-\|multidrug-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP009280.1\|WP_081969919.1\|2786305_2787886_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377924
NZ_CP009280.1\|WP_042135567.1\|2771797_2773618_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP009280.1\|WP_036702452.1\|2780459_2781659_+\|saccharopine-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|224662
NZ_CP009280.1\|WP_042135591.1\|2811947_2812637_+\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP009280.1\|WP_042135572.1\|2777531_2778560_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376439
NZ_CP009280.1\|WP_042135578.1\|2784266_2785250_+\|phosphotransferase	unknown	unknown	gnl\|CDD\|225213
NZ_CP009280.1\|WP_042135570.1\|2776471_2777482_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376439
NZ_CP009280.1\|WP_076248709.1\|2773699_2774611_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042135590.1\|2803192_2811916_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379104
NZ_CP009280.1\|WP_063779791.1\|2774717_2776373_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042135566.1\|2771054_2771669_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379883
NZ_CP009280.1\|WP_042135575.1\|2778602_2779373_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225375
NZ_CP009280.1\|WP_156118587.1\|2789765_2795282_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237081
NZ_CP009280.1\|WP_042135580.1\|2785702_2786290_-\|DUF2441-domain-containing-protein	unknown	unknown	gnl\|CDD\|287372

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_156118587.1\|2789765_2795282_+\|hypothetical-protein	gnl\|CDD\|237081	PRK12372, PRK12372, ribonuclease III; Reviewed.	0.000361812
NZ_CP009280.1\|WP_042135585.1\|2788672_2789326_+\|deoxynucleoside-kinase	gnl\|CDD\|224345	COG1428, COG1428, Deoxynucleoside kinases [Nucleotide transport and metabolism].	3.29702e-87
NZ_CP009280.1\|WP_039303946.1\|2788052_2788676_+\|AAA-family-ATPase	gnl\|CDD\|224345	COG1428, COG1428, Deoxynucleoside kinases [Nucleotide transport and metabolism].	1.15459e-61
NZ_CP009280.1\|WP_156118588.1\|2795282_2803112_+\|hypothetical-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	2.75813e-07
NZ_CP009280.1\|WP_042140990.1\|2781684_2782821_+\|carboxynorspermidine-decarboxylase	gnl\|CDD\|143502	cd06829, PLPDE_III_CANSDC, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Carboxynorspermidine Decarboxylase. Carboxynorspermidine decarboxylase (CANSDC) catalyzes the decarboxylation of carboxynorspermidine, the last step in the biosynthesis of norspermidine. It is homologous to eukaryotic ornithine decarboxylase (ODC) and diaminopimelate decarboxylase (DapDC), which are fold type III PLP-dependent enzymes that contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. Based on this similarity, CANSDC may require homodimer formation and the presence of the PLP cofactor for its catalytic activity.	0
NZ_CP009280.1\|WP_042135565.1\|2769452_2770892_-\|multidrug-efflux-MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	7.24953e-90
NZ_CP009280.1\|WP_081969919.1\|2786305_2787886_-\|hypothetical-protein	gnl\|CDD\|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	9.27742e-17
NZ_CP009280.1\|WP_042135567.1\|2771797_2773618_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	8.55496e-43
NZ_CP009280.1\|WP_036702452.1\|2780459_2781659_+\|saccharopine-dehydrogenase-family-protein	gnl\|CDD\|224662	COG1748, LYS9, Saccharopine dehydrogenase and related proteins [Amino acid transport and metabolism].	6.42709e-171
NZ_CP009280.1\|WP_042135591.1\|2811947_2812637_+\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	2.30664e-22
NZ_CP009280.1\|WP_042135572.1\|2777531_2778560_+\|iron-ABC-transporter-permease	gnl\|CDD\|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	9.58112e-83
NZ_CP009280.1\|WP_042135578.1\|2784266_2785250_+\|phosphotransferase	gnl\|CDD\|225213	COG2334, COG2334, Putative homoserine kinase type II (protein kinase fold) [General function prediction only].	5.85717e-36
NZ_CP009280.1\|WP_042135570.1\|2776471_2777482_+\|iron-ABC-transporter-permease	gnl\|CDD\|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	8.29506e-73
NZ_CP009280.1\|WP_076248709.1\|2773699_2774611_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.07056e-23
NZ_CP009280.1\|WP_042135590.1\|2803192_2811916_+\|hypothetical-protein	gnl\|CDD\|379104	pfam13287, Fn3_assoc, Fn3 associated.	5.54328e-17
NZ_CP009280.1\|WP_063779791.1\|2774717_2776373_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.17007e-23
NZ_CP009280.1\|WP_042135566.1\|2771054_2771669_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	1.52851e-14
NZ_CP009280.1\|WP_042135575.1\|2778602_2779373_+\|alpha/beta-hydrolase	gnl\|CDD\|225375	COG2819, COG2819, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	1.81457e-36
NZ_CP009280.1\|WP_042135580.1\|2785702_2786290_-\|DUF2441-domain-containing-protein	gnl\|CDD\|287372	pfam10386, DUF2441, Protein of unknown function (DUF2441). This is a family of highly conserved, predicted, proteins from Bacillus species. The structure forms a homo-dimer. The function is unknown.	7.10361e-62

>NZ_CP009280.1|WP_042140990.1|2781684_2782821_+|carboxynorspermidine-decarboxylase
MDIDISALPSPAYLVDERLLTKNLETLNYVQEQSGAKILLAQKGFSMHSMYPLVGKYLHGVTSSSLFEARLGFEEMGKEVHVYAPAYVDREFDELLGYTDHIVFNSFDQWSRFKERVQNAPKKISCGIRVNPEYSEIEVPLYDPCYNYSRMGVTLPNFRPEELDGIDGLHFHTMCEQNSDTLERTLKVVEEKFGQYLHGMKWLNFGGGHHITRPDYDLETLIKCIRHMKETYGVEIYLEPGEAIALNTGYLVATVLDTMHNGMDIAILDTSAECHMPDVLAMPYRPGIIGAGMPGEFAHTYRLGGMTCLAGDVIGDYSFPEPLKYGDKLIFLDMAHYSMVKNHMFNGVNLPAIASYNEEEGIKVIREFEYSDFSGRLS
>NZ_CP009280.1|WP_036702452.1|2780459_2781659_+|saccharopine-dehydrogenase-family-protein
MGKALIIGAGGVASVVVHKCCQNPDVFEEICIASRTVSKCDALKEKLDGGLTKISTAKLDADNTEEVIELIKSFQPDVVINVALPYQDLTIMDACLATGVHYVDTANYEPQDTAKFEYSWQWAYKERFEKAGITALLGSGFDPGVTGVFTAYAQKHYFDEIHTIDIVDANAGDHGYPFATNFNPEINIREITANGRYFENGEWIETAPLSEKKVYDLPEIGPKDIYLLYHEELESLAVNIPGVKKIRFWMTFSQNYLTHLKVLENVGMTSIEPINYEGKEIIPLQFLKAILPDPASLGPRTKGKTNIGCIIQGTKDGQPKTYYVYNVCDHEECYREVGSQAISYTTGVPAMIGAMMIIKGIWNKPGVHNIEEFDPDPFMDALNKHGLPWQEDFSPTLLD
>NZ_CP009280.1|WP_042135575.1|2778602_2779373_+|alpha/beta-hydrolase
MGIKYIHIEVHGWKLTIRLPFSYGTEHRRFPVAYLQDEGSVMKHTANYLDHLFRSQQLNELILVGVASKDRNHDYTPWPLPEVTPGAPSFGGGGDDYLRALAEEIKPYIDSHYLTLQEARHTGIIGYSLGGLISLYASYRYPEVFGRIGLLSASFWYEGILDYMRDHPVDRAGQRIYMYYGELEGCYKTNAQKEMAGRSRAAHQLLLEQGFGGGDLLLECDPQGTHDLMFFSRQFPPALKWLFGRGEAGPVRGNAG
>NZ_CP009280.1|WP_042135572.1|2777531_2778560_+|iron-ABC-transporter-permease
MKPKSKALAFWGLFLLLSVLIVCGMYVSLTNGTFDISAKDVVRTLLRIHPVADHDLVIFEFRLPRILLGALVGFGLGIAGAVLQGITRNSLADPGILGIHAAAGAFVVMFMFFVGGTMKAPGWISVMSMPMFGFIGGLCSIVLLYLFARNQGEFHPQQLILVGIALASGFGAVTLYVSLRMDPENFEMATVWLAGSVYNANWRQVLSTLPWLLILTPVIWRRAAVLDLLQLHEVSVKGVGVAVGRERQILLLCCVGLVSACVSVSGSIGFVGLIAPHIARRLIGNTYRYIVPLCGLIGMLMVIIGDFIGKTVFAPFQLPVGIVISIIGVPYFIFLLFRNRAR
>NZ_CP009280.1|WP_042135570.1|2776471_2777482_+|iron-ABC-transporter-permease
MKWTGGIKTASLLVLGVVLIIIISVLSVAYGTKPMSFGTVLNAIFHADPENIDHVIVRTSRIPRTAGALLIGAFLAVSGALMQGMTRNYLASPSIMGISDGSVFAVTLCMVLLPGASSMTMIVYSLAGSALGALLVFGTAKLLPGGVSPLTLAVLGTIIGTFLGGVSQALAVYFQVSQNISFWYNARLHMMDPAVIRLALPFAAAGLVLALLMAKPVTMLSLGDETAAGLGLRVGTIKMLTMLSVVLLTGISVAIAGKIAFIGLIIPHIVRFLVGQDYRKIIPFTAFAGALFLALCDLISRYINFPFETPVGVVTALFGVPFFLYLIKTRGGGHHS
>NZ_CP009280.1|WP_063779791.1|2774717_2776373_+|helix-turn-helix-domain-containing-protein
MELIQQRTSIDNQDDPVDWDRLSFRLLSLQALKGTGEVHLAQQLLFSYALAVVTRGSVQFISDHNQYELAAGSAVLCLPDQTCGTVQPAGGLEMYIFYFDVYCYGKSGDSGSCLPVKDTRLFQGDGRLPFHPSKEMSAKCSRLFLLSEQGEQSIGFRAQLDFQELLYDLRARSLHRPRDTNSALEQAKQYIEAHYTEALTVEQVAQSADFSAKYFVDLYKKKYGKSALEYAAELRIGQAKRLMAESGVKLRDIAHRVGYADEFYFSRKFKKMIGMPPAVYMKSRRRKLAAYTPGLLGQLLPLNITPYAAALHPKWTEYYYRNYRADIPVHISAYRNNQDWQANIEVLKQSNAELILAPAGLADDERTALEQVAPVNYLTSDSADWRGQFHELSRLLGEEWQREQWLAAFDWEVNAAKDRLHEGLGQQTVTVIRMLGSQLFLHCNEGMASILYRELELHPAYECEAEVYNVPVTPAMLAELPADHLLMLIRQEYDTLGEWRKLQNDPQWMKIPAVQRHHVHVLSSDPWREDSAYAQLRMLRQILQLLPANRP
>NZ_CP009280.1|WP_076248709.1|2773699_2774611_+|helix-turn-helix-transcriptional-regulator
MISLSKTLQHLKLISEMLQKRGSQRVEKIVQNLAIDIHWIHDKITFPHWRDIRQNINVHSFYWIQEGQGIFRTDQDYPVSAGMLFYLQPGLAMDMSCGREEPLRITMILLSLYTLSPSADNQGRIEPLDVLPLQFMLKPEGEQGKQLGHMFHKIAADWVPGSTGSQLMTQSLLYELMYELLQVQANAQLGRGQGYELFLRIKDDIERRYSEPLLIHELAVRYGISSSYLRSLFQQYLHRSPKSYLSEIRYEHAGKLLLYTRLTLKEIAAACGYSDEFHFSKSFKQQNGQPPSAMRTQDQGKSG
>NZ_CP009280.1|WP_042135567.1|2771797_2773618_-|acyltransferase
MSEQRSASRKALDYMPWIGPSAQDQQEQILYQQQLTTEYSCTFGEACYVSPEAVVLPDQLQMGDRSYIAGGAIVRSARLVMGSDCSLNSYSVLSGDITMGNGVRVASHASMYGFNHGFASTDIPVFRQPCTVQGIIIGDDVWIGANAVILDGVQIGSHSIVAAGAVVTRDVPAYSIVGGNPARLIRSRLAGDTAAIAAAVEQKEDIGMTMDAQPGGTAVKGGTGTNAADTAVTADKDTAVNTKPVTESVPPYSLLSQQLADFGRLAGDQLIPLLEYYSESTGEENFFRDRPGYKRTVRAYCDAVEIAAMFGSLPPGWTRAELTAVLQGFQDAGTGLLPDPWSPPGPEDLPELLTDHLSRYHLLAVGYALEVLGSALPHPVTVAENMETAALYPYLNDLPWEDNAWGGGDWIDCYATGLYHNLKTFGSRKRPDDLFGWLATHCRRDSGLWGLPTAEEGWLQPVNGFYRLTRATYAQFGLPLPYPERSIDTVLAHSRDRRFFRAEVLNACNVLDVVHPLWLCLKQTDYRRGEIRSWAENMLSEVLKFWVPQRGFAFQLSQQQDTGLQGTEMWLSILYLLADLCGVSSSLGYTPKGVHRLDPAFSLPPR
>NZ_CP009280.1|WP_042135566.1|2771054_2771669_+|TetR/AcrR-family-transcriptional-regulator
MDDIKQENQPKGGRRRGEVLEQAILQAAWEELGEAGYARLTMEGIAVRAQTNKTALYRRWPNKAKIVAAAIKKHMPKTALAAPDSGDLRTDMLQLFQSFARPLQGLGAETIHGLLVDYHGDDLIALLPKIMPPKTGGKLNAIMGTILANAEKRGEVRLDRIPERVILLPLDLFRYELLTTHEPVSDETITGIIDDIFLPLVRIS
>NZ_CP009280.1|WP_042135565.1|2769452_2770892_-|multidrug-efflux-MFS-transporter
MSDQRTKPKKAQKEKLDPAILKVALILVFGALAPLFDSTMINVAIRTLTSDLQSSVAVIQWVITGYVLTMGMAIPVSGWAVNRFGGKKVYMFSLAVFLAGSVLCSLAWNPGSLIGFRLLQGVGAGILIPTLQTVLVQTAGGRNIGRIMSIISIPTLLGPILGPVLGGVIINSLGWRFIFYVNIPITLIAILLAWRGIPADEPSTRKQTLDLTGLLLLSPAFAILIYGIAQISTYGGLHSSKVVIPLVIGLVLMAAFIVYALRTRIEPLLDLRLFKSRIFSASNVTVFLSGMVMNGALLLLPLYYQQVRGESVLSTGMMMIPQGIGMLLTRSWIGSLSDRIGSRIIVILSLLVTIFATLPFAFAGPDTNLILLAAALVVRGAALNGLLIPVMVSAYVGLRKDQIPHASISMRICQTIGGAFGAAILATVSQHQLAGQSASSLQSIAGAYDAAFWWSIGFAVIALIPALILPSHRSSPAAG
>NZ_CP009280.1|WP_042135578.1|2784266_2785250_+|phosphotransferase
MLKLQYLHKNEELAAMLLGNWEHDPESLHLFQYYRISSNAVYPFENAGHSQLLRFAPVTEKQKENILAELEFIAYLREHGYGALEAVSSRTGLELIEAQTPWGPYYASVFKRVAGVQLGSTELSDHIVYKYGEALGRLHQLSNEYTPVQPGRWTHKAVLEWILSVLADFPGEEAAVAEARLLEEYFDGQPVTPENYGLIHYDFEPDNVFYDEASDNINAIDFDDAMYHWYAMDIEQALDSLEGEAAPEEYERKKQIFMNGYISRRPLPQDGPTMAACRRFADLYGYARILRSAAELGENEPDWLTSLRSRLANACAARASRFGGPVG
>NZ_CP009280.1|WP_042135579.1|2785422_2785680_-|hypothetical-protein
MQEAEDEFEDMDEEEDEEDYLTGDYGTRVCDFCGQQADWTEPVNDTNENGEKIELRSCLMCSFDGTGIASREEIQVMMDQMKKRE
>NZ_CP009280.1|WP_042135580.1|2785702_2786290_-|DUF2441-domain-containing-protein
MQVNEWYVYHIVTRNKMDLGQIISFDSNQKNTLYHFFFEKEQMNSKGEDFMQILHGHYTNDGLSMDKENADVVIRYADQTIRAIREALIEMVRLQEYPEYPSRLSCLYAAKSYEDALKWKEIFVSHHRKVLQIVQLRVNGRIFEGDGTLLPKEDGLPFSRKIEQAREYWKGNNHNQLPELLINGIIEVVEIIDEF
>NZ_CP009280.1|WP_081969919.1|2786305_2787886_-|hypothetical-protein
MEGNIFFYLPISVKITLKVEGAFMKKRNLLVSLIMGLTAVLSIGNPETGSAASASGVASYGANYLIKDDGSLWVWGDTKSVPTQVQGLSDVQASFPLWNSALVTARDGSVWNWETNARTLEIEVTPIAELTNMTDFLSLDSRRVAITGEGKVFIAVTTPDGAETTSFSPVPGIDQVAAVSGYSESNGQSSWRRFLFLKTDGTVWTTFDEFATLTPVASLTDITQLEQNYALRKDGSVWTWPIQNFYQPETLGDASKLTATRMPALSSVSILRNNGRTRLAIDGQSRLWFWGSTVTGYSDGTTYADQPVPVLFSGISKVTNAYIVEHSIVALTSDGKVYAASTETTRMSPDAPFTQLTSDVQSMKGGGRHIIMQKKDGTLWGWGVNKNAQLGYGTYEFNYPAPVPMQKPISVTLNGESVAFTNGVITRNGQNFIPLRSLFSKMGATVGYSMDKVATITGTAEGKSPLSIVINTKSGATTVNGKSVTLLTPPFVVNGTVYLPLRFISEQLGATVEWLPQESRITISMK
>NZ_CP009280.1|WP_039303946.1|2788052_2788676_+|AAA-family-ATPase
MKHAPFIAVEGPIGAGKTTLATMLASEMQLPVIKEIVDENPFLDKFYQNMDDWSFQLEMFFLCNRFKQLEDTTTQYIDKGKPVISDYHIYKNLIFGERTLKGSKRDKYREIYHILTDDFPKPDIIFYIRADLDTLLARIAKRARTFEEIIAPAYLQQLIEDYDDAMASLARREPSTVIITIDGNKVDFVENPEDFAAIAEQLKELMK
>NZ_CP009280.1|WP_042135585.1|2788672_2789326_+|deoxynucleoside-kinase
MNSYNIPDNAIITVAGTVGVGKSTLTAALAERLQFQTSLEQVDHNPYLEKFYHDFERWSFHLQIYFLAERFKEQKKMFELGGGFVQDRSIYEDTGIFAKMHADQGTMSKTDYETYTSLYEAMVMTPYFPHPDVLIYIEGSLPSILTRINERGREMEIQTDVSYWEHMHGRYSQWINEFSACPVLRLNIDEYDVKDAASMADILHKVGAAIGRAPVGK
>NZ_CP009280.1|WP_156118587.1|2789765_2795282_+|hypothetical-protein
MLLSLIPGSFSGLAEAAGDDFEVTFKNGAHVGNLSYPAENAFGNFYNNMEEGFAQTETDKDARMDWTTGDIYAGLDDNEATVTFEVDVAKNPLLKAMAESGQAEMITGFAVLRRHSGFLWTRHSAITVTIDGRDIIKERTGSSQKYNKTATARITPTSKIKVWVYGEGDDDGEAAGVRGFYLKFQDLKRPVIDSYTFTGNGAERLNENINQQELYVKRDENITLSYNFNEPVRPATVVKANSDYFLRQKLFINDPDTGLPAAGQQQYLQNITFNEDNLTTYQKTLSYRYTGVPFHNSGNLPLKPLITGGTTGGAPMDLSLENKLKEAVLRDAAGNKATINLNTVPSKSSNAWLNNKSGNPFDFDRGGFRVIVDAVRPKYSKTANGIQPEILTGVTLNKGDVIDFTLQMTEEAIAKTGWDEKKTFILFNNGMKAYYVAGKNTRNWTFRMTVPGGLTVETPLLKVVAVSNDAKGGSLPINMDTDVIQDYAGNLMIQPANFDGIHEEKIDPYGSDFSLANSKIDWANLFIDNTKPIIGYRFEAQGASDVAYSKKGKVTIDANDPSIKVPHLDPTEADRGAERPSRGIYRPSNMSAEASPSVGLVYYWWSQDKADPFASVSGDNNAALKRYALSAKQPSEELYPGEFQNVQLSVVNNKTNLLSPPPEAFEEGNSGEWYLHTWTADMTWDSARELMQYEKKKAYVASHQAQYDAWIAEAPGSKADKIFYADNQALAAVGQYGDLSVWKVDDFKQDDSNWTHEVGILKLDNQGPAITMAAEDSTTVQALVKDPHSGVKSVQYQWVKDGDSPQDIKWADTSYSGNTVTRSTYEDIDEDGAYWLYLKALDNAGNETVKTPQEKAVVVSSEATIPTQFTPEANPDYVRSHDVMFQISGVTPDYVGYAISSSSIHPESDNEYTGLEASTELIQPLSVDNSLDSREETTQPEAPAEPNAPAEPEVTANIGPVAILKLLSEGPVQPELTPLAAEETPAPESGAEPATTPAASAGATEPAADAAAEATEDNTDSRLAAMGLNASVSEATYSYVIPAKSKLNGTQYIHLMVKHSDRTYYYSKAYYFDNEAPVVYFSPDAIAYPLPQQKTRISVSEFYSKTGLVSKYKWVKQETGAEVPTESSTEWKDVPSGGSVSIDDKSLDAGQIAEYRLYVLAVDGAGNSSVTASGGTFKVSASSKPEAPVSDAKSSLIYLSGDAKDGYTAIVKLSLETEDKTGYEYSVSPDNGASWINWKPYTNFVAVKVPTGDPTQLQVWVKYRTPGGLISEAAKLDIEGASTTEQPVYALATLSVNSPVNATVGADIEFTLPPGIRVMPSKINPSVPVRTGNSFKIYENGYYSFDLTDLGDPDRTDTLYLVVKNIDGTPPEGTVEYSNMERTNGNVVAYLQSTSEPVTITNNGGKNAYTFKENGTFVFEIKDAAGNTNTVEATVKNINKEAPKVKVVRSYQYGLNGSSTFNTVKDNNGNVLFSTGTTVTVEKADASAKAINIISQAKSITLTENGTASFTVVDEYGNTTVIKEKVTNILSAPPEADKIAYTFVDADGKAVPADQIVTIGGQKYAKGKVKVTISGSVTAPNKMFFGVRPIEGGAAYSNQISKADGTFSYSRAFESSGSAVVAISDLLGNVNKVPVTIAGLDNTPPELTLNNETAGIVQNKKDFNFRADLGGFTVSDNVSEAAGVKVSVSGLDLSKLGRQRVAYTAVDQVGNETVVYQDVVVVKDGGLLIFGNDTLISASSGESALFNTNTLTFKVSGYNNMKVAGVDKVNQAGTFDILYYPGLYREGQLKLVKQKLTYDELVSSQFKVTFPKTGWYTIVVRTQERDREFATFFIGNMK
>NZ_CP009280.1|WP_156118588.1|2795282_2803112_+|hypothetical-protein
MKDKQGEYMVKLLKRATALMLTIIMVFLSTSESFHALVEAASSTKTTVVENNFIKVTVDNETGRYGIRTVDGQPIRKNDNNVNLLFQGDDPETSFTTFRIDGTDYIYGNKYKFDNSHYSETTTPKVVENSNGTKQLEMIWKIKGVEIKQILMLYTDSKDAVNSGNVNIRYEVNNRSNAQVEIGSRILLDTMVGGNDGPQFQIGTAYKSPLQVERKLVHNPEDNAGIPEEDRAYFKIPSYWVMRDKLDLTNPQATNVVAYGFNNFAEQNINIVDEMIVGHWNGLANTKWDYEVHPNLDFTRDTNDYGTADSAVAFYWNPDKVAAGGFQSFETVYGLGEITAPDKVFSIRYVDQVQQLATAALEQGETVPSKYVDNGVFTITAEVENLQAYNMEHSKIEVEMTLESGLSFVRQDESGKDVLDANGKPVLENDRSKMLEFKKSASPEEAALGIEPKYKPGDAITATFRVQAKGRPWPVTRDYMISARSPETQGKIEGIEDEGIKAQYESNRTNFILLPPVGEATATYSYALSPAELYSSDVKYLTVNLSNIEAYNTGNATTAPNFDLYLKDLVSGSRYKVNVQDAVVMQPTDDGFSGAMRITYRGGERVDEGGNVLESGLGPELPLGEYAVEIDYKGDAGGDEEVAALYDITTPQSFLVTDNDETRIREAGVMAVYREAVDISGLANGASVKDDLLDQLNSLFPGEPFKNGSFLYSAVTEYKKTKALFGAASKAVDPEFDISEFMDDEALKETPLYAYKLFATEEDFEAFQEEAESEDPEFDREVLVTVRGMIKQVGTGDEEQVIVDTKTEPAIINDAVAYTGKDLAFVRGKLDIFGNSLPGDLPFLDTLFIKGDGTLSVASSGFVFHKGEWTLDFFNGFSKSLGDENYNPSKVETPEDDDEEEEGSKEDKGNDGNPEDDSQNGSLKWAIGGVGDRLNPLRQVMIGDVYFNKQSLFGAPSFAIDGFGFSFNDFILRENGISFGGSLSLKIINSEIKNVIFNSAGFYGVDASLGFDLNQEMGLFGPDKKKDADKKKGPDAPSGKVTIKHAVQGGGVGNEYGLEFAAQLKNMLGVEIEFSLKKVKDGRILPDVIAFGAELPAPGIIVTGATYLTAVRGAVRELADTIAGGTAQDPFPLTIEAGVGMRFGIAPAYFFGDVDLTVKRTGLKVEGRLDFSADAEAEKDDRLPMLTKALLEAQWVTPWFVRVEAAMDIGGWDIIIGKAGIFVGQNLEKNRTDFEGYIGSKVQIPNSVPVVGGMPLSSMFLGVNNDKVWGSIGILFISLGITYYWSGGIEFGTSSDQLPEGMIHLVVDDPDNGPRLMVIGEGVETLATSAAPAAEEENQEIIYREVAEGVKIVENGSVNVGVGGITVKNGGRIHEIPMGAATGNAIIEMEYSSKDMPEFKLQDAAGKDYPVVFETFANPDKPNPKANAFTQYIPASDVSPDPSKLNAEVDIRRAYIIIPENEAKKGGTWTLTAVSAVETKLMNVPTLPQLSEVNLAKDNSNVNKFTASWKVANAAEGDTVNLYLAEDAVTTEKTIVEGQEVLSPGDPGMLIAKDVPVGAGGSVSGGITSGSTVIDVTNVTLMGNPEDIRGLLRQGNYYLRAELKSSATFGTKTSPQRFELVDPLAPQVVSDVSVVPAGNGLFSLSFKPGAKKAGHNAYEHSFVIDAQVQVNGKLETYSPFGEILYTEEELQPYWNAATGKYEGILIGGWKALSTSDEVNTTSLEGTVTDVTKLKYTGLEVGTEYVVGVTAATVPTEDADKNQNYHYAEHQNSSKKLLPVPSLPKLTVASGSGTVQDTGNYINLLTSETKQKLTLTSDQSNVTVEVFNAEKSIGSVALTDKAGGGSQGVLNLDQFQTDGPFALELRARNMTTKDISVTMLYMTVDTIAPVLYLDQPVTGERTANGAVHVAGTTTTGTVLTAKYTVNQLQPDGKYKEVEIPTTLKVDPLTGDFNGTVEIKSDEPSVALNIVASDEAKNLNTAVVDITNAGYKVPVALVLKGMEKDLEPGQTGKVKAYLKVSDGQDENTGKPKFKDEPIADKDLQKLTYTVAVGDAVSLSAVGSVTALATGSSLIEAEYKVSEGVTLKGMVAATVAVPKPEKLGAIQASTSYIYADSSRTKITITSSGDMTGQQIAYKVYRSGAVLPAFDDNVSSWSLLPLDGIISASYGDVIVLAKRTSTDKLVKAAGQVTATVWSSSGAGTGGGGGGGGGGGGAATPGVVEEQSPDTAAQVTVNGQPVVTEWNGLTAVIRITDKEAAAGSDLTVSSADPAAKAFSIHVDQNVVKQAVAAKKKVIIEVPMGRLVLEPENLTALNSELVVGIGQNSTADQQAMKTIADQQGFTLMAAGQGVTVTANLPAGSWTPALAAKIAIPSPLAANEITAIVLKDAAGNWTTVPWKLDSSGTAVNVQLTGEGSLYFIRNQKIFKDMPAGWGKDGIAAASAKLFVLGKSADTFDPTGKVTRAEYPTILLRVAGLMNKQAPSAGFSDVGSSSWYNRSVSIAAQLGIVTGFEGGKYAPQGTLTRMEAMTMLGRLLTLVSPGTEISDAEVTAILAGFTDKDKVPAWARQAVALSIKNGIILGEGNKVNPSSPLTREQAAAIAIRLDQLITAKQ
>NZ_CP009280.1|WP_042135590.1|2803192_2811916_+|hypothetical-protein
MALKRKSIIGYLIALAVVVVAAVAGGIMAKADPQTWDSMAKTEWYISTNDTFKIDSEDKLAGVAKLVNEGTGNGLQGKILEITRDMDLKNYQWIPIGTAEHPFKGTLITEGGLIKKISNMNVVTNLSYQGLVGNMEGGTVGGLTFEGSGSITVTGVTYDVYAGSAVGKMSGSSIVFDITNNISISTHASPYRSFTGGIVGMGEGMISNSINNGTITAQGSADIGGILGYGESRGIIIKKVVNNAAILAQGTDSAVLTAGGIAGHTTGPLSLNDEDTPIINNASVTIDGGNRVVAGGIAGKVDNTVVFSNMTTNKGAVTVNASAAEGSAAGALVGATGAVVSPEVGITFVNTAPVVNNGGKNVYTGGIAGYTGSKFTWTHAYINTQPITATGTQDVSTGGFVGHAAGGLVTSNAAAGVFENKALVSVNGVTGIYTGGIAGYDASGNIGQASSTGALNVKGTADVYTGGIVGYEAGGTITSSVTGKTASDLLAITSDGTIGGIAGYLEGTLNDSSVKYATLQVTSAGGIAGGIAGNAQGTMNNITAGDASSASYSTLILKAVVAAPADGQDNITFGGVVGVNTKPLVLTGGKAARISFLNEAGKSGYTIGGAAGKLTADAVIGTVAVPAEVQDLLVELKADKVSFGGGAGHNSAAQFNGHTSRTEIKATGASVKAGGMFGENHSAAAAPFNHAENVVITSTGADNVLGGNTGLNTGQLVNATVTRLSIEANGVRAEAGGIAGHSEGPAAPADRAGMKSAVLNVPGYDPMITLTAVESKAGAIVGAAKTTDITNPEVNAADDAQAFIQAQAAKPSVGGLAGTLENSAIYSDSKIVNLENMLILVAPAATDAYIGGIVGYNEASKLDRLVGTTVNLTINAPRATAGGVAGYNHGSSSGIIVNSYISALNLKANAGAVSSYIGGIVGLNDAQTIDPVLNPATAVSTIQNTRTLGTVSAVSPTSIVGGMVGENRTLIANNSITDKITVISRGNSSIIGGLAGVNTATGTLYYTYSNANLTIEGVGTLGGGLVGENAGAVLGSYVDIDVTGNATGTASGSVYLGGLIGRNTAGTVEQSYTSSKVTANGVYTNVGGLVGEHSGGTIKNSYVAKSVAAAKANSYVGGFIGRITNGKVNNVYSAAQVSAGSGAYAGGFAGRYDNASKELLYKSYYIKDEALNINSDLPDFAEGNHRWLNVHVRLTTILSETLKDRMVFPGLSGWDFEGSWKYGSLNAVYQYPEVNRAANTGGDIGNDVNANINWYMKDKDAINFEITTEAELAGLAAIVNGTIAGADKFDFTDRTVTIMNPIHIQSKQWVPIGNKEANPFEGTFEGNNHLIDGLTLQPVYTHSGLFGVIGTKAIVQNINLEPLSVAGNQYTGVLAGMNLGTVNNVDLKLLGGVKVSGGIVGGMIGSNSGSITGLHLTLDGGSRIETVADHGIAGGLIGENTADFTTGTYTIKDIDGSTGSAADHAIVGGLIGVQTGDVTGLGHEVNSRYRVSATGMESTVGGLIGQFTSGQAKDITLTFADGTLEARGLGSILGGIIGQSDAGNSISNVTVTGFGSGVQLTANGTAGGVVGVKEGKLGGMLARSIDPGNSFDIEHAAVEGVKLSTTGDSLKAVIGGIAGSAVHTAIHDVRFNASLQAAGEEITAGGILGESVNSILYHAEASPDLQVAAKNGDAAVGGIAGTVSADDIHRGYDFGKAYPLYSGIYIAKVQSSKITVTGADNSADLYVGGVAGKNDNASIYSSEVASGLNVTGGNTVNAGGVAGYSSGIIVDTIVKTGLHADTSRVYNAGGLVGWGSGGEIHYSKVIAGSGQALTVGTALTLGQSVPATHAGGVIGMGDTIKITHTHTDIPVQITDTNQDNTIYAGGFAGLLGDNGTLAGQIQKSYAAGKLNVSGRLGSYVGGFAGSVDHYSITDSYASGDISNTGFDTRSGGFAAAVERSGSISNSYALQNKISTVGVKSSTRSYNGGFAGYNDGTLTGVYANVPEISVNVAGNNVSTGALVGYNFRDGKISGSSYTTGTLTAGLKAVGHNAGAAAGAVSSAAVNPLSSGTWIMDYDTSFLNELTDGTITVQTPLQLSGAVMFYNETGLNYYKLFNRTADDKPELATILLGADINLAGSTWTAFDSFKGVFDGQGYTISGLSLKTPEQQTAGFIKENYGQILNVNFTGADISGAVNSGIAAGINHAGAVIRKVNVSGSVAGSATAGGAAGVNLGLIEKAANDGVTLSGQGRKGGIAGRNAGVIHQAVSKGNIDVTATLATGGIAGENSAEGTIFESIVYGDIHVASAQAIAGGISGLNAGEIKNSYSAGAIYAEGMSTAWAGGIAGLAESGAITSSLNTGEVKAGVKGKILPLQAFFGGIAGQKSDHATISQSLFNRQMLKNNIAFYNLDGQAVAGNSSSAMGLLGTELTSPNLPAGLDAGIWTAQNTFYPVLLAFDGTEEGTLASAAVILNPQDLINRVGSAFSLSGSGALVWSADPSKADVNGAAGSLKQGGSAVLKAIAGGQSRSITVNAAALQYPGSAAAPTATPAELSFSTEVKVELTTAEPDGQIYYTLDGTDPTEASQLYSEAIVLKDKTTVKAVTIVPGKEYSKVSAWTWTLLVSSGGGGGGGGGGGGGGGAVVPTPTPTPTPVPVITAIAGTTTVNGDSEAPVKIAKNSKLKLTAPEGQTIYYTTDGSTPTVNSTKYTGELLITKTMTIKMITDKNDTVTTIEYVAENAKYSLKSNAGEIKYIAAYPNGLFMPNAAITRYELIQSLAPLLDMEDVNVGNLFNDVSAGNEALTGFFASAGIIEGYPDGGFGGTKGLTRAEFSKIMTTVLKLDVTDTGITKQSDLKGHWSENYVNALSKAGYVQGFPDGTFKPGSPITRAQAVVLINRIAGTKKLAVTAVRFKDLPATHWAYKDIMSVVQ
>NZ_CP009280.1|WP_042135591.1|2811947_2812637_+|trypsin-like-peptidase-domain-containing-protein
MKTKLLAVSLIFSLISAVLFYSDTTSADTPSVYNAEQSYGIANEAMFYLRVLKSDGTASSTGTGIILSPAGTAATAYHVVKGAERMEGVMADGSIISPIKVTKFDELKDVAVLELPSPAAMKQKGNAYAYLPLRKDVLKHGEAVFALGYPLKNTAIITEGIVNTPAAEINGRSRILTSAQVASGMSGGPLLDTHGQLAGIISGSLRTMNNIHLVVNMEDLRSLLPASFK

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_CP009280_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_5

2783000-2783480

Orphan

Consensus_repeat	Method
CACCATACAACNCACNATA	CRT

7 spacers

The CRISPR arrays of NZ_CP009280_5

>merge|NZ_CP009280|5|2783000-2783480|CRT
CACGATACAACCTATGATAAAGGTCAGCGTACAACACGCCATACTGCTTACCATACAACACATCATATTACTCAACATACAACCACCATACGACCCACGATAAAGCTCAACGTACAACACGCCATACTGTTCACCATACAACCCACGATACTACTCAACATAGAACCACCATACGACCCACATAAAGGTCAGCATACAGCCCACCATACAACACACTATACGACCCACGATAAAGCTCAGCGTACAACACGCGATACTGCTCACCATACAACACACTATACTACTCAACATACAACCACCATACAACCCACATAAAGGTCAGCATACAGCCCACCATACAACACACCATACGACCCACGATAAAGCTCAGCGTACAACACGCGATACTGCTCACCATACAACACACTATACTACTCAACATACAACCTACGTTAAACCTCAGCGTCAACACGCCATATTGTTCACCGTACAATACATCAAT

>NZ_CP009280|5|1|2783000-2783480|CRT
CACGATACAACCTATGATA	AAGGTCAGCGTACAACACGCCATACTGCTTACCATACAACACATCATATTACTCAACATACAAC
CACCATACGACCCACGATA	AAGCTCAACGTACAACACGCCATACTGTT
CACCATACAACCCACGATA	CTACTCAACATAGAACCACCATACGACCCACATAAAGGTCAGCATACAGCC
CACCATACAACACACTATA	CGACCCACGATAAAGCTCAGCGTACAACACGCGATACTGCT
CACCATACAACACACTATA	CTACTCAACATACAACCACCATACAACCCACATAAAGGTCAGCATACAGCC
CACCATACAACACACCATA	CGACCCACGATAAAGCTCAGCGTACAACACGCGATACTGCT
CACCATACAACACACTATA	CTACTCAACATACAACCTACGTTAAACCTCAGCGTCAACACGCCATATTGTT
CACCGTACAATACATCAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042135579.1\|2785422_2785680_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042135585.1\|2788672_2789326_+\|deoxynucleoside-kinase	unknown	unknown	gnl\|CDD\|224345
NZ_CP009280.1\|WP_039303946.1\|2788052_2788676_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|224345
NZ_CP009280.1\|WP_156118588.1\|2795282_2803112_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP009280.1\|WP_042140990.1\|2781684_2782821_+\|carboxynorspermidine-decarboxylase	unknown	unknown	gnl\|CDD\|143502
NZ_CP009280.1\|WP_042135565.1\|2769452_2770892_-\|multidrug-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP009280.1\|WP_081969919.1\|2786305_2787886_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377924
NZ_CP009280.1\|WP_042135567.1\|2771797_2773618_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP009280.1\|WP_036702452.1\|2780459_2781659_+\|saccharopine-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|224662
NZ_CP009280.1\|WP_042135591.1\|2811947_2812637_+\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP009280.1\|WP_042135572.1\|2777531_2778560_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376439
NZ_CP009280.1\|WP_042135578.1\|2784266_2785250_+\|phosphotransferase	unknown	unknown	gnl\|CDD\|225213
NZ_CP009280.1\|WP_042135570.1\|2776471_2777482_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376439
NZ_CP009280.1\|WP_076248709.1\|2773699_2774611_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042135590.1\|2803192_2811916_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379104
NZ_CP009280.1\|WP_063779791.1\|2774717_2776373_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042135566.1\|2771054_2771669_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379883
NZ_CP009280.1\|WP_042135575.1\|2778602_2779373_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|225375
NZ_CP009280.1\|WP_156118587.1\|2789765_2795282_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237081
NZ_CP009280.1\|WP_042135580.1\|2785702_2786290_-\|DUF2441-domain-containing-protein	unknown	unknown	gnl\|CDD\|287372

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_156118587.1\|2789765_2795282_+\|hypothetical-protein	gnl\|CDD\|237081	PRK12372, PRK12372, ribonuclease III; Reviewed.	0.000361812
NZ_CP009280.1\|WP_042135585.1\|2788672_2789326_+\|deoxynucleoside-kinase	gnl\|CDD\|224345	COG1428, COG1428, Deoxynucleoside kinases [Nucleotide transport and metabolism].	3.29702e-87
NZ_CP009280.1\|WP_039303946.1\|2788052_2788676_+\|AAA-family-ATPase	gnl\|CDD\|224345	COG1428, COG1428, Deoxynucleoside kinases [Nucleotide transport and metabolism].	1.15459e-61
NZ_CP009280.1\|WP_156118588.1\|2795282_2803112_+\|hypothetical-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	2.75813e-07
NZ_CP009280.1\|WP_042140990.1\|2781684_2782821_+\|carboxynorspermidine-decarboxylase	gnl\|CDD\|143502	cd06829, PLPDE_III_CANSDC, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Carboxynorspermidine Decarboxylase. Carboxynorspermidine decarboxylase (CANSDC) catalyzes the decarboxylation of carboxynorspermidine, the last step in the biosynthesis of norspermidine. It is homologous to eukaryotic ornithine decarboxylase (ODC) and diaminopimelate decarboxylase (DapDC), which are fold type III PLP-dependent enzymes that contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. Based on this similarity, CANSDC may require homodimer formation and the presence of the PLP cofactor for its catalytic activity.	0
NZ_CP009280.1\|WP_042135565.1\|2769452_2770892_-\|multidrug-efflux-MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	7.24953e-90
NZ_CP009280.1\|WP_081969919.1\|2786305_2787886_-\|hypothetical-protein	gnl\|CDD\|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	9.27742e-17
NZ_CP009280.1\|WP_042135567.1\|2771797_2773618_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	8.55496e-43
NZ_CP009280.1\|WP_036702452.1\|2780459_2781659_+\|saccharopine-dehydrogenase-family-protein	gnl\|CDD\|224662	COG1748, LYS9, Saccharopine dehydrogenase and related proteins [Amino acid transport and metabolism].	6.42709e-171
NZ_CP009280.1\|WP_042135591.1\|2811947_2812637_+\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	2.30664e-22
NZ_CP009280.1\|WP_042135572.1\|2777531_2778560_+\|iron-ABC-transporter-permease	gnl\|CDD\|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	9.58112e-83
NZ_CP009280.1\|WP_042135578.1\|2784266_2785250_+\|phosphotransferase	gnl\|CDD\|225213	COG2334, COG2334, Putative homoserine kinase type II (protein kinase fold) [General function prediction only].	5.85717e-36
NZ_CP009280.1\|WP_042135570.1\|2776471_2777482_+\|iron-ABC-transporter-permease	gnl\|CDD\|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	8.29506e-73
NZ_CP009280.1\|WP_076248709.1\|2773699_2774611_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.07056e-23
NZ_CP009280.1\|WP_042135590.1\|2803192_2811916_+\|hypothetical-protein	gnl\|CDD\|379104	pfam13287, Fn3_assoc, Fn3 associated.	5.54328e-17
NZ_CP009280.1\|WP_063779791.1\|2774717_2776373_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.17007e-23
NZ_CP009280.1\|WP_042135566.1\|2771054_2771669_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	1.52851e-14
NZ_CP009280.1\|WP_042135575.1\|2778602_2779373_+\|alpha/beta-hydrolase	gnl\|CDD\|225375	COG2819, COG2819, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	1.81457e-36
NZ_CP009280.1\|WP_042135580.1\|2785702_2786290_-\|DUF2441-domain-containing-protein	gnl\|CDD\|287372	pfam10386, DUF2441, Protein of unknown function (DUF2441). This is a family of highly conserved, predicted, proteins from Bacillus species. The structure forms a homo-dimer. The function is unknown.	7.10361e-62

>NZ_CP009280.1|WP_042140990.1|2781684_2782821_+|carboxynorspermidine-decarboxylase
MDIDISALPSPAYLVDERLLTKNLETLNYVQEQSGAKILLAQKGFSMHSMYPLVGKYLHGVTSSSLFEARLGFEEMGKEVHVYAPAYVDREFDELLGYTDHIVFNSFDQWSRFKERVQNAPKKISCGIRVNPEYSEIEVPLYDPCYNYSRMGVTLPNFRPEELDGIDGLHFHTMCEQNSDTLERTLKVVEEKFGQYLHGMKWLNFGGGHHITRPDYDLETLIKCIRHMKETYGVEIYLEPGEAIALNTGYLVATVLDTMHNGMDIAILDTSAECHMPDVLAMPYRPGIIGAGMPGEFAHTYRLGGMTCLAGDVIGDYSFPEPLKYGDKLIFLDMAHYSMVKNHMFNGVNLPAIASYNEEEGIKVIREFEYSDFSGRLS
>NZ_CP009280.1|WP_036702452.1|2780459_2781659_+|saccharopine-dehydrogenase-family-protein
MGKALIIGAGGVASVVVHKCCQNPDVFEEICIASRTVSKCDALKEKLDGGLTKISTAKLDADNTEEVIELIKSFQPDVVINVALPYQDLTIMDACLATGVHYVDTANYEPQDTAKFEYSWQWAYKERFEKAGITALLGSGFDPGVTGVFTAYAQKHYFDEIHTIDIVDANAGDHGYPFATNFNPEINIREITANGRYFENGEWIETAPLSEKKVYDLPEIGPKDIYLLYHEELESLAVNIPGVKKIRFWMTFSQNYLTHLKVLENVGMTSIEPINYEGKEIIPLQFLKAILPDPASLGPRTKGKTNIGCIIQGTKDGQPKTYYVYNVCDHEECYREVGSQAISYTTGVPAMIGAMMIIKGIWNKPGVHNIEEFDPDPFMDALNKHGLPWQEDFSPTLLD
>NZ_CP009280.1|WP_042135575.1|2778602_2779373_+|alpha/beta-hydrolase
MGIKYIHIEVHGWKLTIRLPFSYGTEHRRFPVAYLQDEGSVMKHTANYLDHLFRSQQLNELILVGVASKDRNHDYTPWPLPEVTPGAPSFGGGGDDYLRALAEEIKPYIDSHYLTLQEARHTGIIGYSLGGLISLYASYRYPEVFGRIGLLSASFWYEGILDYMRDHPVDRAGQRIYMYYGELEGCYKTNAQKEMAGRSRAAHQLLLEQGFGGGDLLLECDPQGTHDLMFFSRQFPPALKWLFGRGEAGPVRGNAG
>NZ_CP009280.1|WP_042135572.1|2777531_2778560_+|iron-ABC-transporter-permease
MKPKSKALAFWGLFLLLSVLIVCGMYVSLTNGTFDISAKDVVRTLLRIHPVADHDLVIFEFRLPRILLGALVGFGLGIAGAVLQGITRNSLADPGILGIHAAAGAFVVMFMFFVGGTMKAPGWISVMSMPMFGFIGGLCSIVLLYLFARNQGEFHPQQLILVGIALASGFGAVTLYVSLRMDPENFEMATVWLAGSVYNANWRQVLSTLPWLLILTPVIWRRAAVLDLLQLHEVSVKGVGVAVGRERQILLLCCVGLVSACVSVSGSIGFVGLIAPHIARRLIGNTYRYIVPLCGLIGMLMVIIGDFIGKTVFAPFQLPVGIVISIIGVPYFIFLLFRNRAR
>NZ_CP009280.1|WP_042135570.1|2776471_2777482_+|iron-ABC-transporter-permease
MKWTGGIKTASLLVLGVVLIIIISVLSVAYGTKPMSFGTVLNAIFHADPENIDHVIVRTSRIPRTAGALLIGAFLAVSGALMQGMTRNYLASPSIMGISDGSVFAVTLCMVLLPGASSMTMIVYSLAGSALGALLVFGTAKLLPGGVSPLTLAVLGTIIGTFLGGVSQALAVYFQVSQNISFWYNARLHMMDPAVIRLALPFAAAGLVLALLMAKPVTMLSLGDETAAGLGLRVGTIKMLTMLSVVLLTGISVAIAGKIAFIGLIIPHIVRFLVGQDYRKIIPFTAFAGALFLALCDLISRYINFPFETPVGVVTALFGVPFFLYLIKTRGGGHHS
>NZ_CP009280.1|WP_063779791.1|2774717_2776373_+|helix-turn-helix-domain-containing-protein
MELIQQRTSIDNQDDPVDWDRLSFRLLSLQALKGTGEVHLAQQLLFSYALAVVTRGSVQFISDHNQYELAAGSAVLCLPDQTCGTVQPAGGLEMYIFYFDVYCYGKSGDSGSCLPVKDTRLFQGDGRLPFHPSKEMSAKCSRLFLLSEQGEQSIGFRAQLDFQELLYDLRARSLHRPRDTNSALEQAKQYIEAHYTEALTVEQVAQSADFSAKYFVDLYKKKYGKSALEYAAELRIGQAKRLMAESGVKLRDIAHRVGYADEFYFSRKFKKMIGMPPAVYMKSRRRKLAAYTPGLLGQLLPLNITPYAAALHPKWTEYYYRNYRADIPVHISAYRNNQDWQANIEVLKQSNAELILAPAGLADDERTALEQVAPVNYLTSDSADWRGQFHELSRLLGEEWQREQWLAAFDWEVNAAKDRLHEGLGQQTVTVIRMLGSQLFLHCNEGMASILYRELELHPAYECEAEVYNVPVTPAMLAELPADHLLMLIRQEYDTLGEWRKLQNDPQWMKIPAVQRHHVHVLSSDPWREDSAYAQLRMLRQILQLLPANRP
>NZ_CP009280.1|WP_076248709.1|2773699_2774611_+|helix-turn-helix-transcriptional-regulator
MISLSKTLQHLKLISEMLQKRGSQRVEKIVQNLAIDIHWIHDKITFPHWRDIRQNINVHSFYWIQEGQGIFRTDQDYPVSAGMLFYLQPGLAMDMSCGREEPLRITMILLSLYTLSPSADNQGRIEPLDVLPLQFMLKPEGEQGKQLGHMFHKIAADWVPGSTGSQLMTQSLLYELMYELLQVQANAQLGRGQGYELFLRIKDDIERRYSEPLLIHELAVRYGISSSYLRSLFQQYLHRSPKSYLSEIRYEHAGKLLLYTRLTLKEIAAACGYSDEFHFSKSFKQQNGQPPSAMRTQDQGKSG
>NZ_CP009280.1|WP_042135567.1|2771797_2773618_-|acyltransferase
MSEQRSASRKALDYMPWIGPSAQDQQEQILYQQQLTTEYSCTFGEACYVSPEAVVLPDQLQMGDRSYIAGGAIVRSARLVMGSDCSLNSYSVLSGDITMGNGVRVASHASMYGFNHGFASTDIPVFRQPCTVQGIIIGDDVWIGANAVILDGVQIGSHSIVAAGAVVTRDVPAYSIVGGNPARLIRSRLAGDTAAIAAAVEQKEDIGMTMDAQPGGTAVKGGTGTNAADTAVTADKDTAVNTKPVTESVPPYSLLSQQLADFGRLAGDQLIPLLEYYSESTGEENFFRDRPGYKRTVRAYCDAVEIAAMFGSLPPGWTRAELTAVLQGFQDAGTGLLPDPWSPPGPEDLPELLTDHLSRYHLLAVGYALEVLGSALPHPVTVAENMETAALYPYLNDLPWEDNAWGGGDWIDCYATGLYHNLKTFGSRKRPDDLFGWLATHCRRDSGLWGLPTAEEGWLQPVNGFYRLTRATYAQFGLPLPYPERSIDTVLAHSRDRRFFRAEVLNACNVLDVVHPLWLCLKQTDYRRGEIRSWAENMLSEVLKFWVPQRGFAFQLSQQQDTGLQGTEMWLSILYLLADLCGVSSSLGYTPKGVHRLDPAFSLPPR
>NZ_CP009280.1|WP_042135566.1|2771054_2771669_+|TetR/AcrR-family-transcriptional-regulator
MDDIKQENQPKGGRRRGEVLEQAILQAAWEELGEAGYARLTMEGIAVRAQTNKTALYRRWPNKAKIVAAAIKKHMPKTALAAPDSGDLRTDMLQLFQSFARPLQGLGAETIHGLLVDYHGDDLIALLPKIMPPKTGGKLNAIMGTILANAEKRGEVRLDRIPERVILLPLDLFRYELLTTHEPVSDETITGIIDDIFLPLVRIS
>NZ_CP009280.1|WP_042135565.1|2769452_2770892_-|multidrug-efflux-MFS-transporter
MSDQRTKPKKAQKEKLDPAILKVALILVFGALAPLFDSTMINVAIRTLTSDLQSSVAVIQWVITGYVLTMGMAIPVSGWAVNRFGGKKVYMFSLAVFLAGSVLCSLAWNPGSLIGFRLLQGVGAGILIPTLQTVLVQTAGGRNIGRIMSIISIPTLLGPILGPVLGGVIINSLGWRFIFYVNIPITLIAILLAWRGIPADEPSTRKQTLDLTGLLLLSPAFAILIYGIAQISTYGGLHSSKVVIPLVIGLVLMAAFIVYALRTRIEPLLDLRLFKSRIFSASNVTVFLSGMVMNGALLLLPLYYQQVRGESVLSTGMMMIPQGIGMLLTRSWIGSLSDRIGSRIIVILSLLVTIFATLPFAFAGPDTNLILLAAALVVRGAALNGLLIPVMVSAYVGLRKDQIPHASISMRICQTIGGAFGAAILATVSQHQLAGQSASSLQSIAGAYDAAFWWSIGFAVIALIPALILPSHRSSPAAG
>NZ_CP009280.1|WP_042135578.1|2784266_2785250_+|phosphotransferase
MLKLQYLHKNEELAAMLLGNWEHDPESLHLFQYYRISSNAVYPFENAGHSQLLRFAPVTEKQKENILAELEFIAYLREHGYGALEAVSSRTGLELIEAQTPWGPYYASVFKRVAGVQLGSTELSDHIVYKYGEALGRLHQLSNEYTPVQPGRWTHKAVLEWILSVLADFPGEEAAVAEARLLEEYFDGQPVTPENYGLIHYDFEPDNVFYDEASDNINAIDFDDAMYHWYAMDIEQALDSLEGEAAPEEYERKKQIFMNGYISRRPLPQDGPTMAACRRFADLYGYARILRSAAELGENEPDWLTSLRSRLANACAARASRFGGPVG
>NZ_CP009280.1|WP_042135579.1|2785422_2785680_-|hypothetical-protein
MQEAEDEFEDMDEEEDEEDYLTGDYGTRVCDFCGQQADWTEPVNDTNENGEKIELRSCLMCSFDGTGIASREEIQVMMDQMKKRE
>NZ_CP009280.1|WP_042135580.1|2785702_2786290_-|DUF2441-domain-containing-protein
MQVNEWYVYHIVTRNKMDLGQIISFDSNQKNTLYHFFFEKEQMNSKGEDFMQILHGHYTNDGLSMDKENADVVIRYADQTIRAIREALIEMVRLQEYPEYPSRLSCLYAAKSYEDALKWKEIFVSHHRKVLQIVQLRVNGRIFEGDGTLLPKEDGLPFSRKIEQAREYWKGNNHNQLPELLINGIIEVVEIIDEF
>NZ_CP009280.1|WP_081969919.1|2786305_2787886_-|hypothetical-protein
MEGNIFFYLPISVKITLKVEGAFMKKRNLLVSLIMGLTAVLSIGNPETGSAASASGVASYGANYLIKDDGSLWVWGDTKSVPTQVQGLSDVQASFPLWNSALVTARDGSVWNWETNARTLEIEVTPIAELTNMTDFLSLDSRRVAITGEGKVFIAVTTPDGAETTSFSPVPGIDQVAAVSGYSESNGQSSWRRFLFLKTDGTVWTTFDEFATLTPVASLTDITQLEQNYALRKDGSVWTWPIQNFYQPETLGDASKLTATRMPALSSVSILRNNGRTRLAIDGQSRLWFWGSTVTGYSDGTTYADQPVPVLFSGISKVTNAYIVEHSIVALTSDGKVYAASTETTRMSPDAPFTQLTSDVQSMKGGGRHIIMQKKDGTLWGWGVNKNAQLGYGTYEFNYPAPVPMQKPISVTLNGESVAFTNGVITRNGQNFIPLRSLFSKMGATVGYSMDKVATITGTAEGKSPLSIVINTKSGATTVNGKSVTLLTPPFVVNGTVYLPLRFISEQLGATVEWLPQESRITISMK
>NZ_CP009280.1|WP_039303946.1|2788052_2788676_+|AAA-family-ATPase
MKHAPFIAVEGPIGAGKTTLATMLASEMQLPVIKEIVDENPFLDKFYQNMDDWSFQLEMFFLCNRFKQLEDTTTQYIDKGKPVISDYHIYKNLIFGERTLKGSKRDKYREIYHILTDDFPKPDIIFYIRADLDTLLARIAKRARTFEEIIAPAYLQQLIEDYDDAMASLARREPSTVIITIDGNKVDFVENPEDFAAIAEQLKELMK
>NZ_CP009280.1|WP_042135585.1|2788672_2789326_+|deoxynucleoside-kinase
MNSYNIPDNAIITVAGTVGVGKSTLTAALAERLQFQTSLEQVDHNPYLEKFYHDFERWSFHLQIYFLAERFKEQKKMFELGGGFVQDRSIYEDTGIFAKMHADQGTMSKTDYETYTSLYEAMVMTPYFPHPDVLIYIEGSLPSILTRINERGREMEIQTDVSYWEHMHGRYSQWINEFSACPVLRLNIDEYDVKDAASMADILHKVGAAIGRAPVGK
>NZ_CP009280.1|WP_156118587.1|2789765_2795282_+|hypothetical-protein
MLLSLIPGSFSGLAEAAGDDFEVTFKNGAHVGNLSYPAENAFGNFYNNMEEGFAQTETDKDARMDWTTGDIYAGLDDNEATVTFEVDVAKNPLLKAMAESGQAEMITGFAVLRRHSGFLWTRHSAITVTIDGRDIIKERTGSSQKYNKTATARITPTSKIKVWVYGEGDDDGEAAGVRGFYLKFQDLKRPVIDSYTFTGNGAERLNENINQQELYVKRDENITLSYNFNEPVRPATVVKANSDYFLRQKLFINDPDTGLPAAGQQQYLQNITFNEDNLTTYQKTLSYRYTGVPFHNSGNLPLKPLITGGTTGGAPMDLSLENKLKEAVLRDAAGNKATINLNTVPSKSSNAWLNNKSGNPFDFDRGGFRVIVDAVRPKYSKTANGIQPEILTGVTLNKGDVIDFTLQMTEEAIAKTGWDEKKTFILFNNGMKAYYVAGKNTRNWTFRMTVPGGLTVETPLLKVVAVSNDAKGGSLPINMDTDVIQDYAGNLMIQPANFDGIHEEKIDPYGSDFSLANSKIDWANLFIDNTKPIIGYRFEAQGASDVAYSKKGKVTIDANDPSIKVPHLDPTEADRGAERPSRGIYRPSNMSAEASPSVGLVYYWWSQDKADPFASVSGDNNAALKRYALSAKQPSEELYPGEFQNVQLSVVNNKTNLLSPPPEAFEEGNSGEWYLHTWTADMTWDSARELMQYEKKKAYVASHQAQYDAWIAEAPGSKADKIFYADNQALAAVGQYGDLSVWKVDDFKQDDSNWTHEVGILKLDNQGPAITMAAEDSTTVQALVKDPHSGVKSVQYQWVKDGDSPQDIKWADTSYSGNTVTRSTYEDIDEDGAYWLYLKALDNAGNETVKTPQEKAVVVSSEATIPTQFTPEANPDYVRSHDVMFQISGVTPDYVGYAISSSSIHPESDNEYTGLEASTELIQPLSVDNSLDSREETTQPEAPAEPNAPAEPEVTANIGPVAILKLLSEGPVQPELTPLAAEETPAPESGAEPATTPAASAGATEPAADAAAEATEDNTDSRLAAMGLNASVSEATYSYVIPAKSKLNGTQYIHLMVKHSDRTYYYSKAYYFDNEAPVVYFSPDAIAYPLPQQKTRISVSEFYSKTGLVSKYKWVKQETGAEVPTESSTEWKDVPSGGSVSIDDKSLDAGQIAEYRLYVLAVDGAGNSSVTASGGTFKVSASSKPEAPVSDAKSSLIYLSGDAKDGYTAIVKLSLETEDKTGYEYSVSPDNGASWINWKPYTNFVAVKVPTGDPTQLQVWVKYRTPGGLISEAAKLDIEGASTTEQPVYALATLSVNSPVNATVGADIEFTLPPGIRVMPSKINPSVPVRTGNSFKIYENGYYSFDLTDLGDPDRTDTLYLVVKNIDGTPPEGTVEYSNMERTNGNVVAYLQSTSEPVTITNNGGKNAYTFKENGTFVFEIKDAAGNTNTVEATVKNINKEAPKVKVVRSYQYGLNGSSTFNTVKDNNGNVLFSTGTTVTVEKADASAKAINIISQAKSITLTENGTASFTVVDEYGNTTVIKEKVTNILSAPPEADKIAYTFVDADGKAVPADQIVTIGGQKYAKGKVKVTISGSVTAPNKMFFGVRPIEGGAAYSNQISKADGTFSYSRAFESSGSAVVAISDLLGNVNKVPVTIAGLDNTPPELTLNNETAGIVQNKKDFNFRADLGGFTVSDNVSEAAGVKVSVSGLDLSKLGRQRVAYTAVDQVGNETVVYQDVVVVKDGGLLIFGNDTLISASSGESALFNTNTLTFKVSGYNNMKVAGVDKVNQAGTFDILYYPGLYREGQLKLVKQKLTYDELVSSQFKVTFPKTGWYTIVVRTQERDREFATFFIGNMK
>NZ_CP009280.1|WP_156118588.1|2795282_2803112_+|hypothetical-protein
MKDKQGEYMVKLLKRATALMLTIIMVFLSTSESFHALVEAASSTKTTVVENNFIKVTVDNETGRYGIRTVDGQPIRKNDNNVNLLFQGDDPETSFTTFRIDGTDYIYGNKYKFDNSHYSETTTPKVVENSNGTKQLEMIWKIKGVEIKQILMLYTDSKDAVNSGNVNIRYEVNNRSNAQVEIGSRILLDTMVGGNDGPQFQIGTAYKSPLQVERKLVHNPEDNAGIPEEDRAYFKIPSYWVMRDKLDLTNPQATNVVAYGFNNFAEQNINIVDEMIVGHWNGLANTKWDYEVHPNLDFTRDTNDYGTADSAVAFYWNPDKVAAGGFQSFETVYGLGEITAPDKVFSIRYVDQVQQLATAALEQGETVPSKYVDNGVFTITAEVENLQAYNMEHSKIEVEMTLESGLSFVRQDESGKDVLDANGKPVLENDRSKMLEFKKSASPEEAALGIEPKYKPGDAITATFRVQAKGRPWPVTRDYMISARSPETQGKIEGIEDEGIKAQYESNRTNFILLPPVGEATATYSYALSPAELYSSDVKYLTVNLSNIEAYNTGNATTAPNFDLYLKDLVSGSRYKVNVQDAVVMQPTDDGFSGAMRITYRGGERVDEGGNVLESGLGPELPLGEYAVEIDYKGDAGGDEEVAALYDITTPQSFLVTDNDETRIREAGVMAVYREAVDISGLANGASVKDDLLDQLNSLFPGEPFKNGSFLYSAVTEYKKTKALFGAASKAVDPEFDISEFMDDEALKETPLYAYKLFATEEDFEAFQEEAESEDPEFDREVLVTVRGMIKQVGTGDEEQVIVDTKTEPAIINDAVAYTGKDLAFVRGKLDIFGNSLPGDLPFLDTLFIKGDGTLSVASSGFVFHKGEWTLDFFNGFSKSLGDENYNPSKVETPEDDDEEEEGSKEDKGNDGNPEDDSQNGSLKWAIGGVGDRLNPLRQVMIGDVYFNKQSLFGAPSFAIDGFGFSFNDFILRENGISFGGSLSLKIINSEIKNVIFNSAGFYGVDASLGFDLNQEMGLFGPDKKKDADKKKGPDAPSGKVTIKHAVQGGGVGNEYGLEFAAQLKNMLGVEIEFSLKKVKDGRILPDVIAFGAELPAPGIIVTGATYLTAVRGAVRELADTIAGGTAQDPFPLTIEAGVGMRFGIAPAYFFGDVDLTVKRTGLKVEGRLDFSADAEAEKDDRLPMLTKALLEAQWVTPWFVRVEAAMDIGGWDIIIGKAGIFVGQNLEKNRTDFEGYIGSKVQIPNSVPVVGGMPLSSMFLGVNNDKVWGSIGILFISLGITYYWSGGIEFGTSSDQLPEGMIHLVVDDPDNGPRLMVIGEGVETLATSAAPAAEEENQEIIYREVAEGVKIVENGSVNVGVGGITVKNGGRIHEIPMGAATGNAIIEMEYSSKDMPEFKLQDAAGKDYPVVFETFANPDKPNPKANAFTQYIPASDVSPDPSKLNAEVDIRRAYIIIPENEAKKGGTWTLTAVSAVETKLMNVPTLPQLSEVNLAKDNSNVNKFTASWKVANAAEGDTVNLYLAEDAVTTEKTIVEGQEVLSPGDPGMLIAKDVPVGAGGSVSGGITSGSTVIDVTNVTLMGNPEDIRGLLRQGNYYLRAELKSSATFGTKTSPQRFELVDPLAPQVVSDVSVVPAGNGLFSLSFKPGAKKAGHNAYEHSFVIDAQVQVNGKLETYSPFGEILYTEEELQPYWNAATGKYEGILIGGWKALSTSDEVNTTSLEGTVTDVTKLKYTGLEVGTEYVVGVTAATVPTEDADKNQNYHYAEHQNSSKKLLPVPSLPKLTVASGSGTVQDTGNYINLLTSETKQKLTLTSDQSNVTVEVFNAEKSIGSVALTDKAGGGSQGVLNLDQFQTDGPFALELRARNMTTKDISVTMLYMTVDTIAPVLYLDQPVTGERTANGAVHVAGTTTTGTVLTAKYTVNQLQPDGKYKEVEIPTTLKVDPLTGDFNGTVEIKSDEPSVALNIVASDEAKNLNTAVVDITNAGYKVPVALVLKGMEKDLEPGQTGKVKAYLKVSDGQDENTGKPKFKDEPIADKDLQKLTYTVAVGDAVSLSAVGSVTALATGSSLIEAEYKVSEGVTLKGMVAATVAVPKPEKLGAIQASTSYIYADSSRTKITITSSGDMTGQQIAYKVYRSGAVLPAFDDNVSSWSLLPLDGIISASYGDVIVLAKRTSTDKLVKAAGQVTATVWSSSGAGTGGGGGGGGGGGGAATPGVVEEQSPDTAAQVTVNGQPVVTEWNGLTAVIRITDKEAAAGSDLTVSSADPAAKAFSIHVDQNVVKQAVAAKKKVIIEVPMGRLVLEPENLTALNSELVVGIGQNSTADQQAMKTIADQQGFTLMAAGQGVTVTANLPAGSWTPALAAKIAIPSPLAANEITAIVLKDAAGNWTTVPWKLDSSGTAVNVQLTGEGSLYFIRNQKIFKDMPAGWGKDGIAAASAKLFVLGKSADTFDPTGKVTRAEYPTILLRVAGLMNKQAPSAGFSDVGSSSWYNRSVSIAAQLGIVTGFEGGKYAPQGTLTRMEAMTMLGRLLTLVSPGTEISDAEVTAILAGFTDKDKVPAWARQAVALSIKNGIILGEGNKVNPSSPLTREQAAAIAIRLDQLITAKQ
>NZ_CP009280.1|WP_042135590.1|2803192_2811916_+|hypothetical-protein
MALKRKSIIGYLIALAVVVVAAVAGGIMAKADPQTWDSMAKTEWYISTNDTFKIDSEDKLAGVAKLVNEGTGNGLQGKILEITRDMDLKNYQWIPIGTAEHPFKGTLITEGGLIKKISNMNVVTNLSYQGLVGNMEGGTVGGLTFEGSGSITVTGVTYDVYAGSAVGKMSGSSIVFDITNNISISTHASPYRSFTGGIVGMGEGMISNSINNGTITAQGSADIGGILGYGESRGIIIKKVVNNAAILAQGTDSAVLTAGGIAGHTTGPLSLNDEDTPIINNASVTIDGGNRVVAGGIAGKVDNTVVFSNMTTNKGAVTVNASAAEGSAAGALVGATGAVVSPEVGITFVNTAPVVNNGGKNVYTGGIAGYTGSKFTWTHAYINTQPITATGTQDVSTGGFVGHAAGGLVTSNAAAGVFENKALVSVNGVTGIYTGGIAGYDASGNIGQASSTGALNVKGTADVYTGGIVGYEAGGTITSSVTGKTASDLLAITSDGTIGGIAGYLEGTLNDSSVKYATLQVTSAGGIAGGIAGNAQGTMNNITAGDASSASYSTLILKAVVAAPADGQDNITFGGVVGVNTKPLVLTGGKAARISFLNEAGKSGYTIGGAAGKLTADAVIGTVAVPAEVQDLLVELKADKVSFGGGAGHNSAAQFNGHTSRTEIKATGASVKAGGMFGENHSAAAAPFNHAENVVITSTGADNVLGGNTGLNTGQLVNATVTRLSIEANGVRAEAGGIAGHSEGPAAPADRAGMKSAVLNVPGYDPMITLTAVESKAGAIVGAAKTTDITNPEVNAADDAQAFIQAQAAKPSVGGLAGTLENSAIYSDSKIVNLENMLILVAPAATDAYIGGIVGYNEASKLDRLVGTTVNLTINAPRATAGGVAGYNHGSSSGIIVNSYISALNLKANAGAVSSYIGGIVGLNDAQTIDPVLNPATAVSTIQNTRTLGTVSAVSPTSIVGGMVGENRTLIANNSITDKITVISRGNSSIIGGLAGVNTATGTLYYTYSNANLTIEGVGTLGGGLVGENAGAVLGSYVDIDVTGNATGTASGSVYLGGLIGRNTAGTVEQSYTSSKVTANGVYTNVGGLVGEHSGGTIKNSYVAKSVAAAKANSYVGGFIGRITNGKVNNVYSAAQVSAGSGAYAGGFAGRYDNASKELLYKSYYIKDEALNINSDLPDFAEGNHRWLNVHVRLTTILSETLKDRMVFPGLSGWDFEGSWKYGSLNAVYQYPEVNRAANTGGDIGNDVNANINWYMKDKDAINFEITTEAELAGLAAIVNGTIAGADKFDFTDRTVTIMNPIHIQSKQWVPIGNKEANPFEGTFEGNNHLIDGLTLQPVYTHSGLFGVIGTKAIVQNINLEPLSVAGNQYTGVLAGMNLGTVNNVDLKLLGGVKVSGGIVGGMIGSNSGSITGLHLTLDGGSRIETVADHGIAGGLIGENTADFTTGTYTIKDIDGSTGSAADHAIVGGLIGVQTGDVTGLGHEVNSRYRVSATGMESTVGGLIGQFTSGQAKDITLTFADGTLEARGLGSILGGIIGQSDAGNSISNVTVTGFGSGVQLTANGTAGGVVGVKEGKLGGMLARSIDPGNSFDIEHAAVEGVKLSTTGDSLKAVIGGIAGSAVHTAIHDVRFNASLQAAGEEITAGGILGESVNSILYHAEASPDLQVAAKNGDAAVGGIAGTVSADDIHRGYDFGKAYPLYSGIYIAKVQSSKITVTGADNSADLYVGGVAGKNDNASIYSSEVASGLNVTGGNTVNAGGVAGYSSGIIVDTIVKTGLHADTSRVYNAGGLVGWGSGGEIHYSKVIAGSGQALTVGTALTLGQSVPATHAGGVIGMGDTIKITHTHTDIPVQITDTNQDNTIYAGGFAGLLGDNGTLAGQIQKSYAAGKLNVSGRLGSYVGGFAGSVDHYSITDSYASGDISNTGFDTRSGGFAAAVERSGSISNSYALQNKISTVGVKSSTRSYNGGFAGYNDGTLTGVYANVPEISVNVAGNNVSTGALVGYNFRDGKISGSSYTTGTLTAGLKAVGHNAGAAAGAVSSAAVNPLSSGTWIMDYDTSFLNELTDGTITVQTPLQLSGAVMFYNETGLNYYKLFNRTADDKPELATILLGADINLAGSTWTAFDSFKGVFDGQGYTISGLSLKTPEQQTAGFIKENYGQILNVNFTGADISGAVNSGIAAGINHAGAVIRKVNVSGSVAGSATAGGAAGVNLGLIEKAANDGVTLSGQGRKGGIAGRNAGVIHQAVSKGNIDVTATLATGGIAGENSAEGTIFESIVYGDIHVASAQAIAGGISGLNAGEIKNSYSAGAIYAEGMSTAWAGGIAGLAESGAITSSLNTGEVKAGVKGKILPLQAFFGGIAGQKSDHATISQSLFNRQMLKNNIAFYNLDGQAVAGNSSSAMGLLGTELTSPNLPAGLDAGIWTAQNTFYPVLLAFDGTEEGTLASAAVILNPQDLINRVGSAFSLSGSGALVWSADPSKADVNGAAGSLKQGGSAVLKAIAGGQSRSITVNAAALQYPGSAAAPTATPAELSFSTEVKVELTTAEPDGQIYYTLDGTDPTEASQLYSEAIVLKDKTTVKAVTIVPGKEYSKVSAWTWTLLVSSGGGGGGGGGGGGGGGAVVPTPTPTPTPVPVITAIAGTTTVNGDSEAPVKIAKNSKLKLTAPEGQTIYYTTDGSTPTVNSTKYTGELLITKTMTIKMITDKNDTVTTIEYVAENAKYSLKSNAGEIKYIAAYPNGLFMPNAAITRYELIQSLAPLLDMEDVNVGNLFNDVSAGNEALTGFFASAGIIEGYPDGGFGGTKGLTRAEFSKIMTTVLKLDVTDTGITKQSDLKGHWSENYVNALSKAGYVQGFPDGTFKPGSPITRAQAVVLINRIAGTKKLAVTAVRFKDLPATHWAYKDIMSVVQ
>NZ_CP009280.1|WP_042135591.1|2811947_2812637_+|trypsin-like-peptidase-domain-containing-protein
MKTKLLAVSLIFSLISAVLFYSDTTSADTPSVYNAEQSYGIANEAMFYLRVLKSDGTASSTGTGIILSPAGTAATAYHVVKGAERMEGVMADGSIISPIKVTKFDELKDVAVLELPSPAAMKQKGNAYAYLPLRKDVLKHGEAVFALGYPLKNTAIITEGIVNTPAAEINGRSRILTSAQVASGMSGGPLLDTHGQLAGIISGSLRTMNNIHLVVNMEDLRSLLPASFK

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_CP009280_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_7

2897120-2897299

Orphan

Consensus_repeat	Method
AAATCTTGCACAAAATACAACAATC	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP009280_7

>merge|NZ_CP009280|7|2897120-2897299|CRISPRCasFinder
AAATCTTGCACAAAATACAACAATCGCAATGGGCAGACGTCCGAAACTCGGAAATCTTGCACGAAATACAACAATCTGAATTAGTGAGAGCTCAGTTAGGCTGAAATGCTGCATTTTGTACAACAATCGGGGTCCGAGTGGTGCCGTTCCAATGATAATCTTGCATTCTGTACAACATTC

>NZ_CP009280|7|6|2897120-2897299|CRISPRCasFinder
AAATCTTGCACAAAATACAACAATC	GCAATGGGCAGACGTCCGAAACTCGG
AAATCTTGCACGAAATACAACAATC	TGAATTAGTGAGAGCTCAGTTAGGCTG
AAATGCTGCATTTTGTACAACAATC	GGGGTCCGAGTGGTGCCGTTCCAATGA
TAATCTTGCATTCTGTACAACATTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042135696.1\|2903058_2904534_+\|protoporphyrinogen-oxidase	unknown	unknown	gnl\|CDD\|237009
NZ_CP009280.1\|WP_042135688.1\|2898813_2899443_+\|O-methyltransferase	unknown	unknown	gnl\|CDD\|226607
NZ_CP009280.1\|WP_039308750.1\|2886214_2887051_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_039310261.1\|2906943_2907567_+\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP009280.1\|WP_042135686.1\|2897503_2898637_-\|class-I-SAM-dependent-RNA-methyltransferase	unknown	unknown	gnl\|CDD\|223194
NZ_CP009280.1\|WP_042135692.1\|2900940_2902002_+\|uroporphyrinogen-decarboxylase	unknown	unknown	gnl\|CDD\|234644
NZ_CP009280.1\|WP_081969925.1\|2902117_2903062_+\|ferrochelatase	unknown	unknown	gnl\|CDD\|183526
NZ_CP009280.1\|WP_039308765.1\|2895940_2896192_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_039308768.1\|2896318_2896621_+\|heme-biosynthesis-protein-HemY	unknown	unknown	gnl\|CDD\|223393
NZ_CP009280.1\|WP_156118592.1\|2890365_2891970_+\|response-regulator	unknown	unknown	gnl\|CDD\|381091
NZ_CP009280.1\|WP_039308771.1\|2896663_2896903_+\|DUF1450-domain-containing-protein	unknown	unknown	gnl\|CDD\|377806
NZ_CP009280.1\|WP_042135681.1\|2892272_2893625_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|378963
NZ_CP009280.1\|WP_042135683.1\|2893648_2895769_+\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP009280.1\|WP_042141002.1\|2906136_2906868_+\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176506
NZ_CP009280.1\|WP_081969924.1\|2887155_2888559_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP009280.1\|WP_081956787.1\|2899492_2900680_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340949
NZ_CP009280.1\|WP_042135672.1\|2885250_2886189_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP009280.1\|WP_042141003.1\|2907592_2908393_+\|DUF92-domain-containing-protein	unknown	unknown	gnl\|CDD\|376674
NZ_CP009280.1\|WP_042135698.1\|2904723_2906106_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214858
NZ_CP009280.1\|WP_042135677.1\|2888639_2890388_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|225519

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042135696.1\|2903058_2904534_+\|protoporphyrinogen-oxidase	gnl\|CDD\|237009	PRK11883, PRK11883, protoporphyrinogen oxidase; Reviewed.	7.71128e-172
NZ_CP009280.1\|WP_042135688.1\|2898813_2899443_+\|O-methyltransferase	gnl\|CDD\|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	3.05786e-46
NZ_CP009280.1\|WP_039308750.1\|2886214_2887051_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.59101e-76
NZ_CP009280.1\|WP_039310261.1\|2906943_2907567_+\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	1.61092e-56
NZ_CP009280.1\|WP_042135686.1\|2897503_2898637_-\|class-I-SAM-dependent-RNA-methyltransferase	gnl\|CDD\|223194	COG0116, COG0116, Predicted N6-adenine-specific DNA methylase [DNA replication, recombination, and repair].	1.45487e-155
NZ_CP009280.1\|WP_042135692.1\|2900940_2902002_+\|uroporphyrinogen-decarboxylase	gnl\|CDD\|234644	PRK00115, hemE, uroporphyrinogen decarboxylase; Validated.	1.10145e-173
NZ_CP009280.1\|WP_081969925.1\|2902117_2903062_+\|ferrochelatase	gnl\|CDD\|183526	PRK12435, PRK12435, ferrochelatase; Provisional.	1.59644e-122
NZ_CP009280.1\|WP_039308768.1\|2896318_2896621_+\|heme-biosynthesis-protein-HemY	gnl\|CDD\|223393	COG0316, sufA, Fe-S cluster assembly scaffold protein [Posttranslational modification, protein turnover, chaperones].	5.57563e-13
NZ_CP009280.1\|WP_156118592.1\|2890365_2891970_+\|response-regulator	gnl\|CDD\|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.97698e-28
NZ_CP009280.1\|WP_039308771.1\|2896663_2896903_+\|DUF1450-domain-containing-protein	gnl\|CDD\|377806	pfam07293, DUF1450, Protein of unknown function (DUF1450). This family consists of several hypothetical bacterial proteins of around 80 residues in length. Members of this family contain four highly conserved cysteine residues. The function of this family is unknown.	1.07392e-07
NZ_CP009280.1\|WP_042135681.1\|2892272_2893625_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	7.68862e-135
NZ_CP009280.1\|WP_042135683.1\|2893648_2895769_+\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	2.31733e-11
NZ_CP009280.1\|WP_042141002.1\|2906136_2906868_+\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	2.14441e-77
NZ_CP009280.1\|WP_081956787.1\|2899492_2900680_-\|MFS-transporter	gnl\|CDD\|340949	cd17391, MFS_MdtG_MDR_like, Multidrug resistance protein MdtG and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli multidrug resistance protein MdtG, Streptococcus pneumoniae multidrug resistance efflux pump PmrA, and similar multidrug resistance (MDR) transporters from bacteria. 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. MdtG confers resistance to fosfomycin and deoxycholate. PmrA serves as an efflux pump for various substrates and is associated with fluoroquinolone resistance. MdtG-like MDR transporters belong to the bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	5.21339e-129
NZ_CP009280.1\|WP_042135677.1\|2888639_2890388_+\|HAMP-domain-containing-protein	gnl\|CDD\|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	8.12446e-39
NZ_CP009280.1\|WP_042135672.1\|2885250_2886189_+\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.70904e-91
NZ_CP009280.1\|WP_042141003.1\|2907592_2908393_+\|DUF92-domain-containing-protein	gnl\|CDD\|376674	pfam01940, DUF92, Integral membrane protein DUF92. Members of this family have several predicted transmembrane helices. The function of these prokaryotic proteins is unknown.	4.64742e-72
NZ_CP009280.1\|WP_042135698.1\|2904723_2906106_+\|hypothetical-protein	gnl\|CDD\|214858	smart00854, PGA_cap, Bacterial capsule synthesis protein PGA_cap. This protein is a putative poly-gamma-glutamate capsule biosynthesis protein found in bacteria. Poly-gamma-glutamate is a natural polymer that may be involved in virulence and may help bacteria survive in high salt concentrations. It is a surface-associated protein.	2.40563e-94
NZ_CP009280.1\|WP_081969924.1\|2887155_2888559_+\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	7.00128e-32

>NZ_CP009280.1|WP_039308771.1|2896663_2896903_+|DUF1450-domain-containing-protein
MANDIRLCDECNHIKMKSIVPKLLKMAPDAEIKTGCISYCGPCGKRPFVYINGRYISAPTEDEVLAKAEAFVKQPAVKK
>NZ_CP009280.1|WP_039308768.1|2896318_2896621_+|heme-biosynthesis-protein-HemY
MNVKITRNAAKVIKKTMELEGNSELKLRVAITHSHGDHAHYGLDLDTPKENDVVISTDKEIDVILDPNQPLLDGVKIDYLYFPEEGFVITNPSKGNHGDH
>NZ_CP009280.1|WP_039308765.1|2895940_2896192_+|hypothetical-protein
MKFRKLLSLKQWSHIFRSSWQYIISPNVTMGDKLLFTIPALLYWVLPDFMPFIPIDDIGVTMLLMGWFVSRMDRKYPALKSLR
>NZ_CP009280.1|WP_042135683.1|2893648_2895769_+|DUF1080-domain-containing-protein
MTNNHVKHNSSKNRPGRLTILGIVAFLLFSLVSGASGPMAAAAGTTYYVDSALGSDNSSGTSETAAWKTLGKVNSTTFSPGDRILLKAGSVWTNQYLDLQGSGTEGNPITVDRYGSGGKPLIDFGNTAMGGEGFGVRLRNVSYWEINNLEITSGQQPTDMRRNGVLVVGEGAGAGNFRHIYIRNLDIHDIFGTDRRTGGINVHARGANTAPESTWDDILIENNTIINVADTGIQTMTDAFFNSAWTHKFDAFSNVVIRGNVVEKIHRDGILVRASASPLIEYNKTKSIGEATDVNTSIVNYLEDITVVAAQWAYYTKGAIFQYNEASDTRMLGGDGQPWDFDIEVHDSIYQYNYSYNNEGGTLLVMNNTNNNIFRYNISQNDKDANGVFHLVNGGGNLYIYNNIIYRSGTQNKALTHASNTGMAYYTNNIFYNAASGQYTNSPRMTYDHNSFYGLNSGVPSDPNKITGNPGFVSPGTATGLASADGYKLAQTSPLINAGAVVAGNGGLDYFGNTLYNGVPDIGVYEFQGTITPPVTLLQDDFEDNNYSGWTTSGGAWSVADDGTKALTQTSSSGEALAYTGDASWRNYTYSAKIKLLNAFGNAGLLFRYADASNYYMFRLNDSGDKAELFKKTAGTLTMVSSADVAVTPGQWTELKVTVSGSTVTAFAGGTQLIQWTDTAAQPAGGKIGIRMHSSTARIDDVKVTE
>NZ_CP009280.1|WP_042135681.1|2892272_2893625_+|FAD-dependent-oxidoreductase
MNRTTFRLPAEEIAISHEVDVLVAGGGPAGVAAAISAARSGARTLLIEQRGFLGGMGTVALVPAFCPYSDGEKAVVRGIGLQLLEQMKAECEPEFRERFGTELDWVPIDPEVLKRVYDDTVAESGAGVLLHTIASQTVMDADGRKIEGIVIVNKSGRSLIKVKTVIDATGDADLAALAGAPFHKGGEAGELQAATMCYLLANVDRKRFLDYLNESGDTDQIHRAVQQAQADGKLPQGRDSVSGLSWVADYLVGVNFGHVFGIDGSRAEDLTRGAVEGRKLVLRQLEFFRAYVPGFEQAHLVSTGEQIGIRETRRIVGDYVLTQDDFMNMVSFPDDIARNSYFIDIHMARSSGAMHIHHLPPGESHGVPYRCMLPVGLDNVWVAGRAASSDRVVQGSLRVMPNCFAMGQAAGMAAAMAAGTDSQSRKVDITALQRGLVQQGAWLGEALAAL
>NZ_CP009280.1|WP_156118592.1|2890365_2891970_+|response-regulator
MMTLMLIDDDVPMLEYVEYLLGSLGLELQLVASAFSSEDALEQFHAALPDVVIIDIGLPGMDGLELADAFRITKPEVRLIFLTCYEDFHYSKRAIQLEADDYLIKDELSPEQLKSSLSKAMSRFKSREELLERYSFRQAIERNKEVLKQSFLKQLLSGTADQENTLEFGQRLGISWKHPYLRHGFIHMDAASVTERYRYKDIPLIHFAVNNIALELSAGEASITPIMSRDADIYLVWNVADPGCPGTGLTDFMQSVLDKVEQYLKITLRGFYSGASVPLRNFDSLYKTLMDSRDHNFYQAVTPIAVLDEQADFGQTAEWRGDKERGMLSLALEEGHAAWIDLAINQWTQQVTTDRLLPRLVKEACGNFVRQMAFEAGGLAEEDFFTQLEQTVHIQEAARLTKRELRNLWRQHTLAPVAAQEKDIRLQEVDRFLEEHVDQMVTSTDMAEHLHLNASYFSRYFKKLSGINFTDYVNQYKMNMAITMLARPHETVENVAYTLGFSDRAYFSKVFKKYSGRNPSEYKAGPAEEGGAEE
>NZ_CP009280.1|WP_042135677.1|2888639_2890388_+|HAMP-domain-containing-protein
MKWLSRFSFHRRLQFTFLILILLPFIVVTFWSYTSVRENVSDKISRAGEETLKVIGSQIEKTVDSISFVSVYFSEAYDPAVLESLRYLKNTGNFGNYGVYTHYNKLKTTANILSVQSLDADLQIMLVNRENRILIGNQNIPVFSGLPEQLLEESSKLNEQEKISLQWFPYGGDPSAPDYYYAVRFITDPLNQEKLATLYVGIPSHYFHNLLDTGNSANVLSLADGLGRSIAVTGGADTPKESQMLVSEVRIPKVGWLLTSKTPRSSIDSHINREFLVSISIVGLFFLAFLILSMLWAGYINKPISLLRASVKQYVGGNRAVRIPVRGKDEVAVLSSAFNQMLDDMNQLLQQVESEQEEKRLLELQALAAQIRPHFLLNTLNSIKVDLLLSGDQPHGAMIDALMKLLRVYVHVDKPLELAEECKVLGSYVQVMQIRNRLDIAFECVLDEKVGEVMLPRLLLQPIVENAISHGFSARPAKPAILLEAAFEDDMLKISISDNGRGMPEDKLQRLNRRLQGNEDTALWPEKGVGLVNTARRLQVLYGYRARLSAQARTDDDGMTFTLYIPITSEKEAVPLDDPDAD
>NZ_CP009280.1|WP_081969924.1|2887155_2888559_+|extracellular-solute-binding-protein
MSLQTTNQGGIALKKLSLVLASMILMLSVTACGGNGNSTNSAATDAPASADPAAGSSSTDQPAGKAKIKFYTFKADKPEEPIYQAVQAYNESQDKVEVEYESLVQNSDSTDFMKKLDILVAGGEVVDVFMTGNEDELLERASRGVVEPLNSFFEQESITPEDEYSKLLKLDDKVYGILPSSTQWLTVFNKDHLEAAGLSLPEMGWTWDDFRDYAKKLTTPEHYGTYFHTWGEYPNIIAYTEKPHPQLSADLKPIFDDPSFEYFFNLRRTMEKEDKSVEPYADVLASNYHVLQQFFAGNASMLAVPSYAVRAALNLEKFPHEFQTMYAPLPRSVDTEELGMTNISGGGLAMGAKSENKEASYDFIRWMSKESYKFTKEIPAFKGVDGAELINGFFGENTDLIDTASLSKTLFDPNIQMPDTFSVPYGSELKAIVENGFASFILDNRSFDEVKTEMTAEVEKVVQANQK
>NZ_CP009280.1|WP_039308750.1|2886214_2887051_+|carbohydrate-ABC-transporter-permease
MTMRKFKTGNLIFTALFALLSVFFLMPLVWMLSAASKTEKEVWTFPIQWIPTDWNLIANFKAVWMGDVAFGLFYMNSIKIALISTIATIVISAMAGYALGKLDFKGRTLIFTLMLAFMMIPEQATLVPRYIMIKELGLYDSHAALILMGMFSSYFTFLLRQFMIGIHNDMLEAAELDGAGFFRIFWSVVLPLSRPILATVGIIKFIWTWNDYQGPLIMLNSTKLYTIPLGMQFFKEEFGTQISVMMMASVAAILPLLILFLALQKQVIDGIAIGGVKG
>NZ_CP009280.1|WP_042135672.1|2885250_2886189_+|sugar-ABC-transporter-permease
MSESAVTRKTTGAEPKTYWTRKRREQLAGWLFIAPEVIGMLVIAVFPLLFSLFLSLTEWNLVGGLSAIHFVGLDNFVELFRDNRFLLALKNNVLFTIGTVPVTMLLGVVLSALIHKKLYAKTFFKVAFFVPYICSTVAIAAVWQALYHPSKGPINQILMQIGLSEPPRWLVDTSFSLIAIMIIYVWQLLGYQIIIFLAGMTNIPEELYEAATIDGASGIGQFRRITLPLLGPTTFFLAITSTISSFKIFDMIKFLTDGGPNYSSTVIVYQIYEEGFERFKMGYASAMSWVLFLIIMLVTSITWMTQNRKVHY
>NZ_CP009280.1|WP_042135686.1|2897503_2898637_-|class-I-SAM-dependent-RNA-methyltransferase
MGKLQLIATAPMGLEAVVARELNELGYETTVENGRVLFSGDYIDICRCNLWLRTSDRVLVKMGQFPAKTFDELFEGVKAINWEDWIPENGEFPVEGRSHKSQLTSVPACQGIVKKAIVEKLKLSYHTEWFPENGPRYVVEVILLNDIALITLDTTGPALHKRGYRRQATEAPLKETMAAALIQLSRWNGHRPLYDPCCGSGTILIEAAMIAWNIAPGLRRSFPSEHWPEIPQRLWEEAREEAFDAVRDDYPLQLTGTDIDPAAIEIAEAAAKSAGLSGEITFKHIAAAKARPEGEYGCIITNPPYGERISNDKEVEKLTRQFGEMMLYLPTWSFFAISPYKEFEQYYGRKADKRRKLYNGRIECQYYQYLGPLPPRN
>NZ_CP009280.1|WP_042135688.1|2898813_2899443_+|O-methyltransferase
MQNQEEYSEQLYIEDELLLKVKQAIAANGMPEVSIAPGYGRLLTMLVTLSRATRILEIGALGGYSGICLCRGLSQSGSLTSLELNADYGKLAHGHLEQAGFGDAVEYKIGPALDSLKQLEAQGQKYDFFFIDADKENYPNYLEYAIRLASPGAIIAGDNIFLRGRTLNTEKNGPAVQAMRRFNEMIAGDPRLTSTLLPAYDGLALAMVK
>NZ_CP009280.1|WP_081956787.1|2899492_2900680_-|MFS-transporter
MVLWFGQFLVNAGMTMITPFLSLYLAKDLGVTGDHAIGMWAGLIFAANFLTSFIFQPLWGKLADKYGRKIMLLRSSFGMAIVIVLMGFAQSPMQLLLLRLLNGTISGFNPASIALVSGTTPKPRMGFAMGLMQSGAVAGTILGPLIGGLLADWIGFRPIFYVVGALLFVASLLALFLVKEKFDRVEAAQVPQVSVLEGFKELAKVPQLPALFGVTFLLQFAMISPMSLLPLYVEKLHGSAVNIAFWAGMVSAVTGISNMLASPLLGKLSDKVGAHRILTYALIGAALFLIPQAFVTSVWQLILVRFLMGVFMGGLLPSVNALIRSYTPDGKESRAFGFNSSTLALGNMLGAVIGGFLSGYIGIEGLFIISGAFLLINTVWVRLKLYKKTEPRLFR
>NZ_CP009280.1|WP_042135692.1|2900940_2902002_+|uroporphyrinogen-decarboxylase
MTYNDTFIRACRQQSTEHVPVWYMRQAGRYDPEYRKIKEKYSLLEICRQPELAAEVTLMPVRKLGVDAAILYSDIMNPVASLGVDFDIVKNIGPVIENPIRSAADVDRLKPIDVEGDLGHILETIALLDKELDVPLITFAGAPFTIASYLIEGRPSKSYHRTKEMMFSQPRVWEKLMEKLGDMVIAYLRAHVASGGKAFQLFDSWVGALAPRDFEAYVLPTITRIFAELSDLDVPKIYFPGVSSGELLPSLARLQADVIGLDWRVSLTEGRRRTGGGFAIQGNLDPYLLTAPMDVLKERTKELIDEGIRQPGYIFNLGHGLFPEASLDTLKELTDYVHEYSAAALKQAAGPLA
>NZ_CP009280.1|WP_081969925.1|2902117_2903062_+|ferrochelatase
MTTKIGVLVMSYGTPESLEDVEAYYTHIRRGNAPSAEQLKELKDRYEAIVGGVFPLRENTDRQVEALQAKLNSGQIQYVCYQGLKHARPFIEDGVEAMVRDGITQAIGIVLAPHYSVMSVGTYIKRAKEKADACGINMEFVESYHMHPELIDVLSRRVTAKLDEFEETGAARDEVRVLFSAHSLPERILAMGDPYRDQLLETSKAIADQAGVESWQFTWQSAGRTAEPWLGPDILDTLRELAEAQVKYVLSAPIGFVSDHLEVLYDLDIEAQALASELDMRLLRIDSLNSDPAYMSVLSDVVRTKAGQLQVKQS
>NZ_CP009280.1|WP_042135696.1|2903058_2904534_+|protoporphyrinogen-oxidase
MSGSPRKVVIIGGGLSGLSAAYYVRKFYREAGIQPEIILIEKDKCLGGKIETLHRDGFVIEKGPDSFLARKTAMVDLARELELDHELVTTNPNAKKTYILQRGKLHPMPAGLVLGIPTELKPFLKSGLVSFGGKMRAMMDFVLPPRRSSEDESLGDLIERRLGTEVLENMTEPLLAGIYAGDMRKISLQATFPQFGEVERQYGSLIRGMTTGRKPAETHTGTKKSAFLTFRQGLQSLVHALIHDLQDAQQRTGTGAVSIKVRSGAGVSAEASAAPRYEVELDNGELLQADDIYITVQNFAAAELLRPHVDVSALDAVNYVSVANVVMAFTKKGIVTEYDGSGFLVPRKEGRNITACTWTSTKWLHTSPDDKVLLRCYVGRSGDEQNVDLPDEALAELVRKDLKEIMGITAAPLFTEITRLRHSMPQYPVGHPGRIAGLRSELEEKLPGVYAFGAGYDGIGMPDCIKQAKLTAETAAAHLEKLPEQPAAVTV
>NZ_CP009280.1|WP_042135698.1|2904723_2906106_+|hypothetical-protein
MYPPRSRSRQSKKHSSKKRRRTVWAWFNVVLLLMITGLLAYSFMDNKEKESSAPPVAVTEPSPSPEASATAAAPVEVAPTAEATASPEPTPEATPEATALPTETAEAVITPVSTVKEAAATAEPQATTGNPGGLISGLPENSSGGTVKLNFAGDVIFAGKVAELLQKKGYDYSYSALDGMFKKDDLTVVNLETPITTGGVGAANKQFVFKGAPEALDALKSAGVDAVNLANNHTLDQGEEGLLDTLKHLSKRGIPYVGAGKNSKEAYSAQYFERQGIKIALLGFTRVMPVIEWKAEAGKPGLASVYDSAEALKAIAAAKQQADLVVVVVHWGKERMEQYDKTQQTLGHSFIDAGADLVMGGHPHVLQGIEPYKGKWIAYSTGNFIFTRSSLPATWETAVFQAECSKEGQCSLKLSPMDAELGQPVPMNEADGQLLLHKVESLSSGLVKIRNDGTVVQSAQ
>NZ_CP009280.1|WP_042141002.1|2906136_2906868_+|glycerophosphodiester-phosphodiesterase
MNNMCVAHRGFSGKAPENTLAAVRMAIALPFVRWMEIDVQLTKDGVPVVIHDYSLDRTTNGHGKVKNMDYEHIRRLDAGSWKGRAFRGERVPSLEEVLSLASGRLRLNIELKTSGEMYPGLEQAVIDLVNTMGMREDVVLTSFDAGALQRIKELDPRFRTGLIYDSRSGDPAKKLNELGCSFLSISSDRLSPVLAKSLAERGVKIMAWTVNKAKEMRRLSAMHSDIMICTNRPDIWGDIFLQA
>NZ_CP009280.1|WP_039310261.1|2906943_2907567_+|fumarylacetoacetate-hydrolase-family-protein
MSRAVNNVYCVGRNYKLHAEELGNQVPAEPLIFLKPSHAAVALDKAIIHLPKDAGLIHYEGELVLRIARDYVPGMSVEELVDVMALGLDFTLRDVHNDLQKKGLPWTPAKGFKNAAPLTPYIAFPEQEELEATDFTVRKNGIEVQRGNVQNMIFSLQKIVEFIASRYGLGKDDIIFTGTPAGVGPVVPGDSFELFWGDTLMGTCLIG
>NZ_CP009280.1|WP_042141003.1|2907592_2908393_+|DUF92-domain-containing-protein
MQWLIGACGALLVAGAAYWKQSLSLSGMLAAIVMGTIYFGAGNAFWFGILLLFFISSSLLSKLHHENKAELEATYDKTGRRDAGQVFANGGLGMLLVLLNAIYPLEIWGFLFIGVMATVTSDTWATEIGTLAKRPPRSVLTGKVLQAGTSGGVSLPGTLAAAAGGALIGAASWLLRAASGMPPHSLLTLALAGLLGGLAGAFADSVLGATVQRMNRCAVCGREVEASMHCGKPTLYARGWRWMDNDTVNAVSSIIGGVVALLASYI

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_CP009280_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_8

2913991-2914089

Orphan

Consensus_repeat	Method
ATGATTCAGTCCACACAGCCTAAGCTCTCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_8

>merge|NZ_CP009280|8|2913991-2914089|CRISPRCasFinder
ATGATTCAGTCCACACAGCCTAAGCTCTCCGTAAACCCCGCAGCATGGCATTAGCCTTCATAGTCTCCATGATTCAGTCCTCACAGCCTAAGCTCTCCG

>NZ_CP009280|8|7|2913991-2914089|CRISPRCasFinder
ATGATTCAGTCCACACAGCCTAAGCTCTCCG	TAAACCCCGCAGCATGGCATTAGCCTTCATAGTCTCC
ATGATTCAGTCCTCACAGCCTAAGCTCTCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042135696.1\|2903058_2904534_+\|protoporphyrinogen-oxidase	unknown	unknown	gnl\|CDD\|237009
NZ_CP009280.1\|WP_036725228.1\|2918175_2918373_+\|cold-shock-domain-containing-protein	unknown	unknown	gnl\|CDD\|278729
NZ_CP009280.1\|WP_036702226.1\|2917769_2918003_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_144026086.1\|2912379_2912703_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_156118774.1\|2913112_2913910_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042135719.1\|2922472_2924947_+\|pyridine-nucleotide-disulfide-oxidoreductase	unknown	unknown	gnl\|CDD\|163244
NZ_CP009280.1\|WP_039299701.1\|2921262_2922234_+\|6-phosphofructokinase	unknown	unknown	gnl\|CDD\|235111
NZ_CP009280.1\|WP_144026094.1\|2920160_2921189_+\|DUF2600-family-protein	unknown	unknown	gnl\|CDD\|378492
NZ_CP009280.1\|WP_039310261.1\|2906943_2907567_+\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP009280.1\|WP_042135698.1\|2904723_2906106_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214858
NZ_CP009280.1\|WP_042135702.1\|2909128_2911072_+\|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223562
NZ_CP009280.1\|WP_042135721.1\|2924962_2925223_+\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197390
NZ_CP009280.1\|WP_042141002.1\|2906136_2906868_+\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176506
NZ_CP009280.1\|WP_042135710.1\|2914114_2915158_-\|M42-family-metallopeptidase	unknown	unknown	gnl\|CDD\|349907
NZ_CP009280.1\|WP_042135712.1\|2915185_2915506_-\|DUF1049-domain-containing-protein	unknown	unknown	gnl\|CDD\|227703
NZ_CP009280.1\|WP_042135717.1\|2918637_2919882_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340893
NZ_CP009280.1\|WP_042135700.1\|2908469_2909072_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP009280.1\|WP_042141003.1\|2907592_2908393_+\|DUF92-domain-containing-protein	unknown	unknown	gnl\|CDD\|376674
NZ_CP009280.1\|WP_042141004.1\|2915591_2917382_-\|oligoendopeptidase-F	unknown	unknown	gnl\|CDD\|341071
NZ_CP009280.1\|WP_081970469.1\|2911589_2912009_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|315378

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042135696.1\|2903058_2904534_+\|protoporphyrinogen-oxidase	gnl\|CDD\|237009	PRK11883, PRK11883, protoporphyrinogen oxidase; Reviewed.	7.71128e-172
NZ_CP009280.1\|WP_036725228.1\|2918175_2918373_+\|cold-shock-domain-containing-protein	gnl\|CDD\|278729	pfam00313, CSD, 'Cold-shock' DNA-binding domain.	9.08426e-32
NZ_CP009280.1\|WP_042135721.1\|2924962_2925223_+\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|197390	cd10155, BsYrkD-like_DUF156, Uncharacterized protein YrkD from Bacillus subtilis and related domains; this domain superfamily was previously known as part of DUF156. This domain family contains an uncharacterized protein YrkD from Bacillus subtilis and related proteins. This family is part of a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes CsoRs (copper-sensitive operon repressors). CsoRs form homotetramers (dimer of dimers). In Mycobacterium tuberculosis CsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily. In this family, however, not all these residues are conserved, there is an Asn instead of the His (C-N-C); also a conserved Tyr and a Glu residue that facilitates allosteric regulation of DNA binding for CsoRs are very poorly conserved.	1.42933e-33
NZ_CP009280.1\|WP_042135719.1\|2922472_2924947_+\|pyridine-nucleotide-disulfide-oxidoreductase	gnl\|CDD\|163244	TIGR03385, Coenzyme_A_disulfide_reductase, CoA-disulfide reductase. Members of this protein family are CoA-disulfide reductase (EC 1.8.1.14), as characterized in Staphylococcus aureus, Pyrococcus horikoshii, and Borrelia burgdorferi, and inferred in several other species on the basis of high levels of CoA and an absence of glutathione as a protective thiol. [Cellular processes, Detoxification].	2.19112e-172
NZ_CP009280.1\|WP_039299701.1\|2921262_2922234_+\|6-phosphofructokinase	gnl\|CDD\|235111	PRK03202, PRK03202, ATP-dependent 6-phosphofructokinase.	0
NZ_CP009280.1\|WP_144026094.1\|2920160_2921189_+\|DUF2600-family-protein	gnl\|CDD\|378492	pfam10776, DUF2600, Protein of unknown function (DUF2600). This is a bacterial family of proteins. Some members in the family are annotated as YtpB however currently no function is known.	0
NZ_CP009280.1\|WP_039310261.1\|2906943_2907567_+\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	1.61092e-56
NZ_CP009280.1\|WP_042135698.1\|2904723_2906106_+\|hypothetical-protein	gnl\|CDD\|214858	smart00854, PGA_cap, Bacterial capsule synthesis protein PGA_cap. This protein is a putative poly-gamma-glutamate capsule biosynthesis protein found in bacteria. Poly-gamma-glutamate is a natural polymer that may be involved in virulence and may help bacteria survive in high salt concentrations. It is a surface-associated protein.	2.40563e-94
NZ_CP009280.1\|WP_042135702.1\|2909128_2911072_+\|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	0
NZ_CP009280.1\|WP_042141002.1\|2906136_2906868_+\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	2.14441e-77
NZ_CP009280.1\|WP_042135710.1\|2914114_2915158_-\|M42-family-metallopeptidase	gnl\|CDD\|349907	cd05657, M42_glucanase_like, M42 Peptidase, endoglucanase-like subfamily. Peptidase M42 family, glucanase (endo-1,4-beta-glucanase or endoglucanase)-like subfamily. Proteins in this subfamily are co-catalytic metallopeptidases, found in archaea and bacteria. They show similarity to cellulase and endo-1,4-beta-glucanase (endoglucanase) which typically bind two zinc or cobalt atoms. Some of the enzymes exhibit typical aminopeptidase specificity, whereas others are also capable of N-terminal deblocking activity, i.e. hydrolyzing acylated N-terminal residues. Many of these enzymes are assembled either as tetrahedral dodecamers or as octahedral tetracosameric structures, with the active site located on the inside such that substrate sizes are limited, indicating function as possible peptide scavengers.	5.47705e-154
NZ_CP009280.1\|WP_042135712.1\|2915185_2915506_-\|DUF1049-domain-containing-protein	gnl\|CDD\|227703	COG5416, COG5416, Uncharacterized integral membrane protein [Function unknown].	4.84837e-16
NZ_CP009280.1\|WP_042135717.1\|2918637_2919882_-\|MFS-transporter	gnl\|CDD\|340893	cd17335, MFS_MFSD6, Major facilitator superfamily domain-containing protein 6. Human Major facilitator superfamily domain-containing protein 6 (MFSD6) is also called macrophage MHC class I receptor 2 homolog (MMR2). It has been postulated as a possible receptor for human leukocyte antigen (HLA)-B62. MFSD6 is conserved through evolution and appeared before bilateral animals. It belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.33304e-51
NZ_CP009280.1\|WP_042135700.1\|2908469_2909072_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	4.56697e-16
NZ_CP009280.1\|WP_042141003.1\|2907592_2908393_+\|DUF92-domain-containing-protein	gnl\|CDD\|376674	pfam01940, DUF92, Integral membrane protein DUF92. Members of this family have several predicted transmembrane helices. The function of these prokaryotic proteins is unknown.	4.64742e-72
NZ_CP009280.1\|WP_042141004.1\|2915591_2917382_-\|oligoendopeptidase-F	gnl\|CDD\|341071	cd09608, M3B_PepF, Peptidase family M3B, oligopeptidase F (PepF). Peptidase family M3B oligopeptidase F (PepF; Pz-peptidase B; EC 3.4.24.-) is mostly bacterial and includes oligoendopeptidase F from Lactococcus lactis. This enzyme hydrolyzes peptides containing between 7 and 17 amino acids with fairly broad specificity. The PepF gene is duplicated in L. lactis on the plasmid that bears it, while a shortened second copy is found in Bacillus subtilis. Most bacterial PepFs are cytoplasmic endopeptidases; however, the Bacillus amyloliquefaciens PepF oligopeptidase is a secreted protein and may facilitate the process of sporulation. Specifically, the yjbG gene encoding the homolog of the PepF1 and PepF2 oligoendopeptidases of Lactococcus lactis has been identified in Bacillus subtilis as an inhibitor of sporulation initiation when over-expressed from a multicopy plasmid. This PepF family includes Streptococcus agalactiae PepB, a group B streptococcal oligopeptidase which has been shown to degrade a variety of bioactive peptides as well as the synthetic collagen-like substrate N-(3-[2-furyl]acryloyl)-Leu-Gly- Pro-Ala in vitro.	0
NZ_CP009280.1\|WP_081970469.1\|2911589_2912009_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|315378	pfam12688, TPR_5, Tetratrico peptide repeat. BH0479 of Bacillus halodurans is a hypothetical protein which contains a tetratrico peptide repeat (TPR) structural motif. The TPR motif is often involved in mediating protein-protein interactions. This protein is likely to function as a dimer. The first 48 amino acids are not present in the clone construct. This Pfam entry includes tetratricopeptide-like repeats not detected by the pfam00515, pfam07719, pfam07720 and pfam07221 models.	2.08027e-06

>NZ_CP009280.1|WP_156118774.1|2913112_2913910_-|hypothetical-protein
MQSLRGHRRWWIVVTTVVLLVLFAVILAALRLTDDDEHEVFDDLPHSYIYAESSGEIQLHMMAVKPEDIVLRRAGQPLRQIAAYGINGGFFYGDDLLSIAIMNDVPVNGAPQGYGSGWFNAKYERGTLVWDGAAGAFSVQVVASGGDLAVSDRGNYWAQGGISMNLQHEELWAAGAAAEHLPFEGERRLRSGLVYDQSGKLWLLVTNSLCTAAEFRTAVQRAVPGEGREGIFLDGDGSSQMNADEVVLTGDSRPVVQMIAVAGGK
>NZ_CP009280.1|WP_144026086.1|2912379_2912703_+|hypothetical-protein
MMNIRLREIGLSVMFVSAVFFFGRPDVTDETNEHIEHNVEALKYYKNTSAPVIAHPISADNKLPRRHEETSEQNLIIAEVDSGKSPVQLIPVYKNGDVPRIELVPSR
>NZ_CP009280.1|WP_081970469.1|2911589_2912009_+|tetratricopeptide-repeat-protein
MLLQLLSADDSNAELYYQLAWTHDVLGMEREAVSYYEQSLAHGLPDEEQKAGAMLGLGSTYRTLGAYSQSRELLEQGVLEFPHRAEFKAFLAMTLHNLGAHAEAMELLLKLLSETSADAGIHSYSKAIMFYADKLEQVW
>NZ_CP009280.1|WP_042135702.1|2909128_2911072_+|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MNIMTVEHLSKSYGEKTLFLDASFGMDDRDKIGVIGVNGTGKSTFLKIIAGLDTPDAGQIAIGNDVRVQYLAQNPPYEPGNTVLQQVFAGDDPELATMREYMEIMSLLEQNPGDSGLEARLVRIGQAIDAAGSWQLESEAKIVLTKLGITQFDARMENLSGGQRKRVALAAALITPSELLILDEPTNHIDTDSVAWLEQYLQKRRGALLMVTHDRYFLERVASVMLELDGGSLYRYEANYSRFLELKADREEREASAEQKRKNLLRTELAWIRRGAKARSTKQKARIDRFEKLKESTGGASSASMDISVASTRLGRKIIEIQDLTKSMDGRTLIKDLTYIAVPQDRVGIVGKNGSGKSTLLNLIAGKLTPDSGEVQLGTTVKLGYFTQEHQDMDLSMRAIEYVKEEAEIIKTADGSVITAGQMLERFLFPPAMQWTPISKLSGGEKRRLYLLRVLMGAPNVLLLDEPTNDLDIGTLAVLEDYLDEFPGVVFTVSHDRYFLDRTIDKLIAFEDGSIRLHVGDYSEYEEWLAKNVPSGSGGSGKSEGAGGRSTTAPVEQSGNAPAAAPSREKLKFTFKEQKEYEGIDEAIEQAEQHLVDISAEMEAAFADSGKLQELVDKQRQAEAELERLMERWTYLNELAEKIAGKA
>NZ_CP009280.1|WP_042135700.1|2908469_2909072_+|TetR/AcrR-family-transcriptional-regulator
MSSASVHKHAAILDAAYELFGSGGFYETKMSEVAERAGIAKGTVYLYFKSKEELFMAVTRRDCEGFLEQLEGKLGTCSRLADKLSVIAEHHLFYYYERKQHTKLFFRAPNNNPELVDYMAQFMEAYMQAVVKVLLEGGASEPELMAQSYIGMLDRLKMDILFNPGFAEEDAYKRAKFAANLFITGALGSLNSALGDLPSE
>NZ_CP009280.1|WP_042141003.1|2907592_2908393_+|DUF92-domain-containing-protein
MQWLIGACGALLVAGAAYWKQSLSLSGMLAAIVMGTIYFGAGNAFWFGILLLFFISSSLLSKLHHENKAELEATYDKTGRRDAGQVFANGGLGMLLVLLNAIYPLEIWGFLFIGVMATVTSDTWATEIGTLAKRPPRSVLTGKVLQAGTSGGVSLPGTLAAAAGGALIGAASWLLRAASGMPPHSLLTLALAGLLGGLAGAFADSVLGATVQRMNRCAVCGREVEASMHCGKPTLYARGWRWMDNDTVNAVSSIIGGVVALLASYI
>NZ_CP009280.1|WP_039310261.1|2906943_2907567_+|fumarylacetoacetate-hydrolase-family-protein
MSRAVNNVYCVGRNYKLHAEELGNQVPAEPLIFLKPSHAAVALDKAIIHLPKDAGLIHYEGELVLRIARDYVPGMSVEELVDVMALGLDFTLRDVHNDLQKKGLPWTPAKGFKNAAPLTPYIAFPEQEELEATDFTVRKNGIEVQRGNVQNMIFSLQKIVEFIASRYGLGKDDIIFTGTPAGVGPVVPGDSFELFWGDTLMGTCLIG
>NZ_CP009280.1|WP_042141002.1|2906136_2906868_+|glycerophosphodiester-phosphodiesterase
MNNMCVAHRGFSGKAPENTLAAVRMAIALPFVRWMEIDVQLTKDGVPVVIHDYSLDRTTNGHGKVKNMDYEHIRRLDAGSWKGRAFRGERVPSLEEVLSLASGRLRLNIELKTSGEMYPGLEQAVIDLVNTMGMREDVVLTSFDAGALQRIKELDPRFRTGLIYDSRSGDPAKKLNELGCSFLSISSDRLSPVLAKSLAERGVKIMAWTVNKAKEMRRLSAMHSDIMICTNRPDIWGDIFLQA
>NZ_CP009280.1|WP_042135698.1|2904723_2906106_+|hypothetical-protein
MYPPRSRSRQSKKHSSKKRRRTVWAWFNVVLLLMITGLLAYSFMDNKEKESSAPPVAVTEPSPSPEASATAAAPVEVAPTAEATASPEPTPEATPEATALPTETAEAVITPVSTVKEAAATAEPQATTGNPGGLISGLPENSSGGTVKLNFAGDVIFAGKVAELLQKKGYDYSYSALDGMFKKDDLTVVNLETPITTGGVGAANKQFVFKGAPEALDALKSAGVDAVNLANNHTLDQGEEGLLDTLKHLSKRGIPYVGAGKNSKEAYSAQYFERQGIKIALLGFTRVMPVIEWKAEAGKPGLASVYDSAEALKAIAAAKQQADLVVVVVHWGKERMEQYDKTQQTLGHSFIDAGADLVMGGHPHVLQGIEPYKGKWIAYSTGNFIFTRSSLPATWETAVFQAECSKEGQCSLKLSPMDAELGQPVPMNEADGQLLLHKVESLSSGLVKIRNDGTVVQSAQ
>NZ_CP009280.1|WP_042135696.1|2903058_2904534_+|protoporphyrinogen-oxidase
MSGSPRKVVIIGGGLSGLSAAYYVRKFYREAGIQPEIILIEKDKCLGGKIETLHRDGFVIEKGPDSFLARKTAMVDLARELELDHELVTTNPNAKKTYILQRGKLHPMPAGLVLGIPTELKPFLKSGLVSFGGKMRAMMDFVLPPRRSSEDESLGDLIERRLGTEVLENMTEPLLAGIYAGDMRKISLQATFPQFGEVERQYGSLIRGMTTGRKPAETHTGTKKSAFLTFRQGLQSLVHALIHDLQDAQQRTGTGAVSIKVRSGAGVSAEASAAPRYEVELDNGELLQADDIYITVQNFAAAELLRPHVDVSALDAVNYVSVANVVMAFTKKGIVTEYDGSGFLVPRKEGRNITACTWTSTKWLHTSPDDKVLLRCYVGRSGDEQNVDLPDEALAELVRKDLKEIMGITAAPLFTEITRLRHSMPQYPVGHPGRIAGLRSELEEKLPGVYAFGAGYDGIGMPDCIKQAKLTAETAAAHLEKLPEQPAAVTV
>NZ_CP009280.1|WP_042135710.1|2914114_2915158_-|M42-family-metallopeptidase
MLNIQPNEEYILTLLKKLLDTPSPSGFTAQVMTLVAEEAAALNIPLSWNEKGGAILTVPGLDPSRTIGISAHVDTLGAMVRSIKPNGSLRLTSVGGFSMQSIENEYCTIHTRSGLTYTGTILSSHPSVHVYADARDFKRVEENMEIRIDEVVSTKDDVLKLGIAVGDFISFDARAVLTPSGYVKSRHLDDKASVAAIFGLLESIRREGWKPLHNLSLLISNYEEVGHGAAWIPGGINEMIAVDMGAMGDDLSCKETDVSICAKDSSGPYDYAMTSKLIELANGLAIPFAVDIYPQYGSDASAALRGGNNIRAALIGPGVHASHSMERTHKQAVLNTAKLLAAYVGAH
>NZ_CP009280.1|WP_042135712.1|2915185_2915506_-|DUF1049-domain-containing-protein
MKFQWSLILGLFFALLTAVFAVMNVDTVPVNFGFDVVSIPLILVILGCALIGGVVVGSYGIFRQYKLQKQIKSLNAELTKLRDAGNAMDSLTVPNDVLSSEGSAQI
>NZ_CP009280.1|WP_042141004.1|2915591_2917382_-|oligoendopeptidase-F
MEQLPKRSEVPAENRWKLEDMFASEEQWDAEYKEVKELITSASDFQGKLDSPQALKKCFELDDKLSLLTERLYVYAHMRQDEDTAAPKYQALSSKAKKLGVEAGEALSFVTPEILALPNETLDQFIADPSLSDYTFTLTEMKREKAHVLSKAEEALLAQVGTLAQAPQTVFGMLNNADLKFPKVKNEDGEEVELTHGSYIQFLESPDREVRKNAFKAVYETYGKQKNTIAATLSANVNKNVFYSRVRKYPSVLEMSLYGDNIPKEVYTNLIDTIHESLPLMHRYMKLRQKLLGVDELHMYDLFAPLVDEYKLNITFEEAKKITKEGLKPLGEDYLSVLQEGYDKSWIDVYENENKRTGAYSWGAYGTHPYVLLNHNDNLNSMFTLAHEMGHALHSYYSDTTLKYRDAQYTIFLAEVASTTNEALLMDYLLNKSTDPKEKMYLLTYYADQFRTTVFRQTMFAEFEKIIHQRAEEGESLTPQDLSAIYYDLNVKYYGKDMVVDKDIEMEWARIPHFYNSFYVYKYATGFSAATSFAKQILEEGKPAVDRYLGFLKSGGSDYSINILTKAGVDMSSPEPIREAMSVFESVIEQMEQLTK
>NZ_CP009280.1|WP_036702226.1|2917769_2918003_-|hypothetical-protein
MIKKHEIYKTDKWNMMTVEVQGRYIILREISDQWGEETHTFMSRPAMMQWVNNRFNKESYKDNEEEYKNIIAAFKQV
>NZ_CP009280.1|WP_036725228.1|2918175_2918373_+|cold-shock-domain-containing-protein
MKGTVKWFNAEKGYGFLQVEGGEDVFVHFSAIQGDGFKTLDEGQAVEFDVTDGNRGPQAANVVKL
>NZ_CP009280.1|WP_042135717.1|2918637_2919882_-|MFS-transporter
MYAGRSGGQYSDQNWLRSFMFTLYGTSVLVVSYFPLFYSHLGFSSPQMGLLYSVGPLISILSNLFWSMMSDRLGTVRKIMALLLGGQLVTAIILARAADFSSVMLILSVFYFFYYPVFPLADTMAIKIAQRHGRNFIAIRVFGSLGYSFFALTIGYVLRALGPEYSVGICIVIVVTALLITFGLKDVKRSEPAPADVSGDASGKPLKGGGLKEILLQKEVLWFFSCVFLLAIGYRMNEAFLTISLKGMNAGDEIIGWALLASALSEIPIFFLLSKYGDKFKELPLLAFASLMFALRFLFMSLAQEPGAVVAIQAMHSVSFGIYYVTAVRYITRIIPDHLRATGMALFTVVWSSGAGLLSGTFGGLIYQDAGRIVFYMVATGFSILAFIGFLSKHLMDVGGGPDRPLRRKARTPL
>NZ_CP009280.1|WP_144026094.1|2920160_2921189_+|DUF2600-family-protein
MNRVYKYVLPEVRACLDFWRQDAEGIPDPELRKQALASIETKQFHCEGGGIYAAGNLSMRHILIPLIVAYQTISDYLDNLCDRSTSLDPADFRLLHQSMLDAINPEAEPVNYYALRNEQNDGGYLYRLVRKCQEMTSQLPGYAAAAAEIHDLAVLYTDLQVYKHIRPELREAALKEWWEREGHRAPHLGWNEFAAATGSTLGVFMLFLASCDPKLSLSASASIRAAYFPHVCGLHIMLDYLIDQDEDRAGGDLNFCNYYDDTDTMLNRIASIVEWARKDVRTLPETSMHRMVIEGLLALYLSDPKVSEQREVRSVSKRLMRKSPLTRLFFFVNSRWIRKHMY
>NZ_CP009280.1|WP_039299701.1|2921262_2922234_+|6-phosphofructokinase
MANVKKIAVLTSGGDSQGMNAAVRAVVRSAIYFGIEVFGIQRGYQGLLNRDIFPMDLRSVGDIIQRGGTILQSARCLEFLKPEGQQRGADILNEMGIDGLVVIGGDGSYKGANKLSKLGINTMALPGTIDNDISFTDYTIGFDTAVGVVVDAINKLRDTMSSHERSSIVEVMGRHCGDIALHAGLASGAETILVPEMPYDLNEVADRMKDNFARGKRHSIVIVAEGVGKGEDVAQALKDRHASLDARVTVLGHIQRGGTPTPGDRNLASRLGDFAVRKLIEGESDKACGIIKGELTLTDIDKVVNTKKDFDTDLYELASRLSQ
>NZ_CP009280.1|WP_042135719.1|2922472_2924947_+|pyridine-nucleotide-disulfide-oxidoreductase
MGRTIVIIGGVAGGASAAARLRRLNEEDRIIILERGEHVSFANCGLPYYIGETIDSREKLFLQTPAGIRARFNIDVRVFTEATQIDREHKRVECRNSKTGEVEQIPYDIIVLSPGARPIVPSIEGISAAENLFTLRNIPDTDRIKAYVDRRKPRHATVIGAGFIGLEMAENLRERGLEVTVIDRGQQILNPLDPEMARPLEEHMRLHGVEVRLNEGVEAFEQQGSLLRLSSGEVLSTDMVILAIGVSPENDLARSSGLALGVRGAVKVNAQLQTSDPAIYAVGDVIEVKDRIQGFDTMVSLAWGANRQGRLAADHINGREASYNGAMGTAIIKIFGLTAALTGNNEKTLKSLGVPYEAVHIHPNSHAGYYPGAAPIAMKLLFNPQTGAIYGAQAAGSTGVDKRIDVIATAIRGNLKANELADIELSYAPPYSSAKDPVNMAGYVASNLLEGLVANLQWHEVDDFSHGGGLIIDVREEVERSAGYIPGSINIPLPELRERLTEIPRDKEIAVSCQVGLRGYIAARILSQNGYQVRNVDGGYKTYAVMEESQLQSTGKRKASSGSAAPANAVNNRTEHGNEQRLILDACGLQCPGPILKVYETVKSMEDGQRVEISATDFGFAADIRQWCSKTHNTLESVDVSEGKVKALVRKGSWNTADDVFQVQNPQVTEGTTMVVFSGDLDKTIASFIIASGAAAMGKQVTMFFTFWGLNVLRRGQTPQVKKAGLDRMFGMMMPQGTRKLPLSRMNMGGLGARLIRYTMKRKNVDSLEQLMQGALNAGVKLMACSMSMDIMGISQEELIEGVEIGGVASYLGAAEDSGVNLFI
>NZ_CP009280.1|WP_042135721.1|2924962_2925223_+|metal-sensitive-transcriptional-regulator
MVYDKAIINRLKRIEGQVRGVLSMLEEGKDCREIVTQLTAIRTAVDRTAGAVIGDNLEHCIQEELAKGNTPDQVIKEAVQLLVKSR

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_CP009280_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_9

3120317-3120664

Orphan

Consensus_repeat	Method
AAAGGGATAAATCCCACTAATTCCGCCGAAAGTGGGCGATGC	PILER-CR

3 spacers

The CRISPR arrays of NZ_CP009280_9

>merge|NZ_CP009280|9|3120317-3120664|PILER-CR
AAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATGCACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCAATGTGCGGAAATGAAAGGGATAAATCCCACTAATTCCGCCGAAAGTGGGCGATGCACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATGTGCGGGAATGAAAGGGATAAATCCCACTAATTCCGCCGAAAGTGGGCGATGCACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATACGCGGAAATGAAAGGGATAAATCCCACTAATTCCGCCGAAAGTCGGCGATGT

>NZ_CP009280|9|1|3120317-3120664|PILER-CR
AAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATGC	ACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCAATGTGCGGAAATG
AAAGGGATAAATCCCACTAATTCCGCCGAAAGTGGGCGATGC	ACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATGTGCGGGAATG
AAAGGGATAAATCCCACTAATTCCGCCGAAAGTGGGCGATGC	ACGGGAATCAAAGGGATAAATCCCTCTAATTCCGCCGAAAGTGGGCGATACGCGGAAATG
AAAGGGATAAATCCCACTAATTCCGCCGAAAGTCGGCGATGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_081969936.1\|3126467_3128375_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|225519
NZ_CP009280.1\|WP_042135892.1\|3108537_3109965_+\|family-43-glycosylhydrolase	unknown	unknown	gnl\|CDD\|350132
NZ_CP009280.1\|WP_042135917.1\|3130347_3131778_+\|family-43-glycosylhydrolase	unknown	unknown	gnl\|CDD\|350117
NZ_CP009280.1\|WP_042135902.1\|3116481_3117501_+\|zinc-binding-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|176222
NZ_CP009280.1\|WP_042135921.1\|3133522_3134314_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_156118598.1\|3119801_3119963_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042135913.1\|3125011_3126544_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|227095
NZ_CP009280.1\|WP_042135894.1\|3111098_3113543_+\|DUF5110-domain-containing-protein	unknown	unknown	gnl\|CDD\|269877
NZ_CP009280.1\|WP_052421801.1\|3122968_3123955_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_CP009280.1\|WP_042135904.1\|3117522_3119769_+\|glycoside-hydrolase-family-95-protein	unknown	unknown	gnl\|CDD\|379625
NZ_CP009280.1\|WP_042135919.1\|3131801_3133316_+\|glycosyl-hydrolase-43-family-protein	unknown	unknown	gnl\|CDD\|350115
NZ_CP009280.1\|WP_042135900.1\|3115522_3116482_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381389
NZ_CP009280.1\|WP_042135908.1\|3121192_3122875_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270300
NZ_CP009280.1\|WP_042135891.1\|3107131_3108277_-\|xylanase	unknown	unknown	gnl\|CDD\|225940
NZ_CP009280.1\|WP_042135923.1\|3134486_3136301_+\|family-43-glycosylhydrolase	unknown	unknown	gnl\|CDD\|350139
NZ_CP009280.1\|WP_042135898.1\|3114555_3115395_+\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|226145
NZ_CP009280.1\|WP_042135910.1\|3123969_3124881_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_052421802.1\|3128367_3129888_+\|response-regulator	unknown	unknown	gnl\|CDD\|227095
NZ_CP009280.1\|WP_052421800.1\|3110104_3110998_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042135896.1\|3113554_3114424_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_081969936.1\|3126467_3128375_+\|sensor-histidine-kinase	gnl\|CDD\|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.57702e-45
NZ_CP009280.1\|WP_042135892.1\|3108537_3109965_+\|family-43-glycosylhydrolase	gnl\|CDD\|350132	cd18620, GH43_XylA-like, Glycosyl hydrolase family 43-like protein such as Clostridium stercorarium alpha-L-arabinofuranosidase XylA. This glycosyl hydrolase family 43 (GH43) subgroup belongs to the GH43_AXH-like subgroup which includes enzymes that have been characterized with beta-xylosidase (EC 3.2.1.37), alpha-L-arabinofuranosidase (EC 3.2.1.55), alpha-1,2-L-arabinofuranosidase 43A (arabinan-specific; EC 3.2.1.-), endo-alpha-L-arabinanase as well as arabinoxylan arabinofuranohydrolase (AXH) activities. GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. The GH43_XylA-like subgroup includes Clostridium stercorarium alpha-L-arabinofuranosidase XylA, and enzymes that have been annotated as having beta-xylosidase (EC 3.2.1.37), alpha-L-arabinofuranosidase (EC 3.2.1.55), endo-alpha-L-arabinanase (EC 3.2.1.-) as well as arabinoxylan arabinofuranohydrolase (AXH) activities. GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. AXHs specifically hydrolyze the glycosidic bond between arabinofuranosyl substituents and xylopyranosyl backbone residues of arabinoxylan.	1.78704e-139
NZ_CP009280.1\|WP_042135917.1\|3130347_3131778_+\|family-43-glycosylhydrolase	gnl\|CDD\|350117	cd09003, GH43_XynD-like, Glycosyl hydrolase family 43 protein such as Bacillus subtilis arabinoxylan arabinofuranohydrolase (XynD;BsAXH-m23;BSU18160). This glycosyl hydrolase family 43 (GH43) subgroup includes characterized Bacillus subtilis arabinoxylan arabinofuranohydrolase (AXH), Caldicellulosiruptor sp. Tok7B.1 beta-1,4-xylanase (EC 3.2.1.8) / alpha-L-arabinosidase (EC 3.2.1.55) XynA, Caldicellulosiruptor sp. Rt69B.1 xylanase C (EC 3.2.1.8) XynC, and Caldicellulosiruptor saccharolyticus beta-xylosidase (EC 3.2.1.37)/ alpha-L-arabinofuranosidase (EC 3.2.1.55) XynF. It belongs to the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. It belongs to the GH43_AXH-like subgroup which includes enzymes that have been annotated as having beta-xylosidase, alpha-L-arabinofuranosidase and arabinoxylan alpha-L-1,3-arabinofuranohydrolase, xylanase (endo-alpha-L-arabinanase) as well as AXH activities. GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. AXHs specifically hydrolyze the glycosidic bond between arabinofuranosyl substituents and xylopyranosyl backbone residues of arabinoxylan. Bacillus subtilis AXH (BsAXH-m2,3) has been shown to cleave arabinose units from O-2- or O-3-mono-substituted xylose residues and superposition of its structure with known structures of the GH43 exo-acting enzymes, beta-xylosidase and alpha-L-arabinanase, each in complex with their substrate, reveals a different orientation of the sugar backbone. Several of these enzymes also contain carbohydrate binding modules (CBMs) that bind cellulose or xylan. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	0
NZ_CP009280.1\|WP_042135902.1\|3116481_3117501_+\|zinc-binding-alcohol-dehydrogenase-family-protein	gnl\|CDD\|176222	cd08261, Zn_ADH7, Alcohol dehydrogenases of the MDR family. This group contains members identified as related to zinc-dependent alcohol dehydrogenase and other members of the MDR family. 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 includes various 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.	5.93867e-172
NZ_CP009280.1\|WP_042135921.1\|3133522_3134314_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.8977e-24
NZ_CP009280.1\|WP_042135913.1\|3125011_3126544_+\|response-regulator-transcription-factor	gnl\|CDD\|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	3.38625e-86
NZ_CP009280.1\|WP_042135894.1\|3111098_3113543_+\|DUF5110-domain-containing-protein	gnl\|CDD\|269877	cd06591, GH31_xylosidase_XylS, xylosidase XylS-like. XylS is a glycosyl hydrolase family 31 (GH31) alpha-xylosidase found in prokaryotes, eukaryotes, and archaea, that catalyzes the release of alpha-xylose from the non-reducing terminal side of the alpha-xyloside substrate. XylS has been characterized in Sulfolobus solfataricus where it hydrolyzes isoprimeverose, the p-nitrophenyl-beta derivative of isoprimeverose, and xyloglucan oligosaccharides, and has transxylosidic activity. All GH31 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. The XylS family corresponds to subgroup 3 in the Ernst et al classification of GH31 enzymes.	1.65187e-168
NZ_CP009280.1\|WP_042135908.1\|3121192_3122875_+\|extracellular-solute-binding-protein	gnl\|CDD\|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.40392e-155
NZ_CP009280.1\|WP_042135904.1\|3117522_3119769_+\|glycoside-hydrolase-family-95-protein	gnl\|CDD\|379625	pfam14498, Glyco_hyd_65N_2, Glycosyl hydrolase family 65, N-terminal domain. This domain represents a domain found to the N-terminus of the glycosyl hydrolase 65 family catalytic domain.	3.37636e-87
NZ_CP009280.1\|WP_042135919.1\|3131801_3133316_+\|glycosyl-hydrolase-43-family-protein	gnl\|CDD\|350115	cd09001, GH43_FsAxh1-like, Glycosyl hydrolase family 43 such as Fibrobacter succinogenes subsp. succinogenes S85 arabinoxylan alpha-L-arabinofuranosidase. This glycosyl hydrolase family 43 (GH43) includes mostly enzymes that have been annotated as having beta-1,4-xylosidase (beta-D-xylosidase; xylan 1,4-beta-xylosidase; EC 3.2.1.37) activity. They are part of an array of hemicellulases that are involved in the final breakdown of plant cell-wall whereby they degrade xylan. They hydrolyze beta-1,4 glycosidic bonds between two xylose units in short xylooligosaccharides. These are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. This subfamily includes the characterized Clostridium stercorarium F-9 beta-xylosidase Xyl43B. It also includes Humicola insolens AXHd3 (HiAXHd3), a GH43 arabinofuranosidase (EC 3.2.1.55) that hydrolyzes O3-linked arabinose of doubly substituted xylans, a feature of the polysaccharide that is recalcitrant to degradation. It possesses an additional C-terminal beta-sandwich domain such that the interface between the domains comprises a xylan binding cleft that houses the active site pocket. The HiAXHd3 active site is tuned to hydrolyze arabinofuranosyl or xylosyl linkages, and the topology of the distal regions of the substrate binding surface confers specificity. It also includes Fibrobacter succinogenes subsp. succinogenes S85 arabinoxylan alpha-L-arabinofuranosidase (Axh1;Fisuc_1769;FSU_2269), Paenibacillus sp. E18 alpha-L-arabinofuranosidase (Abf43A), Bifidobacterium adolescentis ATCC 15703 double substituted xylan alpha-1,3-L-specific arabinofuranosidase d3 (AXHd3;AXH-d3;BaAXH-d3;BAD_0301;E-AFAM2), and Chrysosporium lucknowense C1 arabinoxylan hydrolase / double substituted xylan alpha-1,3-L-arabinofuranosidase (Abn7;AXHd). A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	4.08702e-133
NZ_CP009280.1\|WP_042135900.1\|3115522_3116482_+\|aldo/keto-reductase	gnl\|CDD\|381389	cd19163, AKR_galDH, L-galactose dehydrogenase (L-galDH) and similar proteins. L-galDH (EC 1.1.1.316), also called L-galactose 1-dehydrogenase, catalyzes the oxidation of L-galactose to L-galactono-1,4-lactone in the presence of NAD(+). It uses NAD(+) as a hydrogen acceptor much more efficiently than NADP(+).	1.57756e-172
NZ_CP009280.1\|WP_052421801.1\|3122968_3123955_+\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	9.62598e-128
NZ_CP009280.1\|WP_042135891.1\|3107131_3108277_-\|xylanase	gnl\|CDD\|225940	COG3405, CelA, Endoglucanase Y [Carbohydrate transport and metabolism].	2.0159e-88
NZ_CP009280.1\|WP_042135923.1\|3134486_3136301_+\|family-43-glycosylhydrolase	gnl\|CDD\|350139	cd18818, GH43_GbtXyl43B-like, Glycosyl hydrolase family 43 such as Geobacillus thermoleovorans IT-08 beta-xylosidase/exo-xylanase (GbtXyl43B). This glycosyl hydrolase family 43 (GH43) subgroup includes the characterized enzymes Geobacillus thermoleovorans IT-08 beta-xylosidase (EC 3.2.1.37) / exo-xylanase (GbtXyl43B), and Paenibacillus sp. strain E18 alpha-L-arabinofuranosidase (EC 3.2.1.55) Abf43B. It belongs to the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	1.16483e-159
NZ_CP009280.1\|WP_042135898.1\|3114555_3115395_+\|amidohydrolase-family-protein	gnl\|CDD\|226145	COG3618, COG3618, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	1.2312e-59
NZ_CP009280.1\|WP_042135910.1\|3123969_3124881_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.74205e-57
NZ_CP009280.1\|WP_052421802.1\|3128367_3129888_+\|response-regulator	gnl\|CDD\|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.86333e-69
NZ_CP009280.1\|WP_052421800.1\|3110104_3110998_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.69223e-26
NZ_CP009280.1\|WP_042135896.1\|3113554_3114424_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	4.41535e-27

>NZ_CP009280.1|WP_156118598.1|3119801_3119963_+|hypothetical-protein
MEDCVNWMLAELMIIENCVNRKLAERMIIEDYGNRKLAEWMIIEDCGNRKLAE
>NZ_CP009280.1|WP_042135904.1|3117522_3119769_+|glycoside-hydrolase-family-95-protein
MTSKEQSQRLWYSEPAQEWNEALPIGNGRLGAMIFGRAAEEKLQLNEDSVWYGGPRDRNNEDALPHLPKLRKLILEGKLKEAEELAAMTMTGLPEAQRHYLPLGELLLSFSGHEQPAADYRRELDLERGVSRVSYSTGGVRYTRELFASFPDQAIVVRLTSDRKNAISLKARFNRQNWRMLEKTEKWQNSGLVMGGECGGRGGSSFAAVLKAVTEDGTCRNIGEYLLVEGANSVTLLLAAGTTFRHPDPALHAKMQLEELSRVPYEELLARHIADYRSLYGRVALTLPENPQLHGLPTGERLKRFQQGEEDHWLITTYFQYGRYLLISSSRPGSLPANLQGIWNDSFTPAWDSKFTININAQMNYWPAEICNLAECHEPLFDLIERMREPGRVTARVMYDCGGFTAHHNTDIWADTAPQDTYLPASFWPLGAAWLCLHLWEHYQFSQDRYYLAQAYDTMKEAAQFLLDYLIEDEAGRLITCPSVSPENTYQLPGGESGVLCAGASMDFQIIEALFKAVVRSAEIIGRDEAFREELRSALDRLPGPQIGKYGQIQEWMEDYEEVEPGHRHISHLFALYPGDAFTVEHTPELAAAARTTLERRLASGGGHTGWSRAWIINFWARLQDESKAYTNVRALLEHSTLPNLFDNHPPFQIDGNFGGTAGIAEMLLQSHTDSIRLLPALPASWSEGSVKGLRARGGYTLDFSWADGLVTEAVVSCTVSGPCRIEGPGLDSVFFIGEAGGSYTFTR
>NZ_CP009280.1|WP_042135902.1|3116481_3117501_+|zinc-binding-alcohol-dehydrogenase-family-protein
MKGIICEEIGKLVYREDLPEPELQDGEAIVSIRRIGICGTDLHAYRGNQPYFTYPRVLGHELSGTVERIGDNPQGLRAGDQVSVIPYLHCGECRACLSGTTNCCQKMRVFGVHLDGGMRERVSLPVGNLLKTDGLTLDQAAMLEPLAIGAHAVRRSGLGSGDQVLVIGAGPIGLGVMAMARYAGAQVIAMDVNDERLEFCKGWAQAEHTVSALREPKEQLSGLTQGNFLPYVIDSTGNISSMEGAFGLVGHGGTLTYVGLVKGDITFSDPDFHAREMTVQGSRNATREDFEQVIRAITDGYIEVDSYISHRCSFEDMTGQFESWLNPESKVIKALVELD
>NZ_CP009280.1|WP_042135900.1|3115522_3116482_+|aldo/keto-reductase
MKYRKLGNTGLEVSVLSYGASSLGSVFRDVPKEEGIRTVHTALDMGINLIDVSPYYGLTKAETVLGESLQTVPRDRYILSTKAGRYGQDEFDFSRERIIRSAEESMGRLGTDYLDILLLHDIEFGSLEQVMEEGIPALEELKQSGKIRYSGVTGLPLPIFETVLSRTALDVILSYCHYSLNDTALLQLLPLLESRGTGLINASPISMGLLSNRKVPDWHPASAEIQAACQRAAEYCRDNGEDIAKLAVQFSTANEQIPTTLVSTATPENIRNNIKWTDEPMDEQLLAEVRGILKPIDGATWPSGQPEWNVMQGRNGDLL
>NZ_CP009280.1|WP_042135898.1|3114555_3115395_+|amidohydrolase-family-protein
MYIDAHQHYWKIDRDDYGWITPDIPVLFRDYLPADLEPHLHKHGISHSIVVQAAPTVEETEYILGLSEQADSIAGVIGWLDLTSPSFKEQYQQLCRHRKFTGLRVMIQEMEDPGLLLTRPYIEALTFLADEDVPVDLLVLADQLPQLIGLLDRVPGLRGVIDHLAKPPIAAGQLEPWRSRMAEIAKHPGICCKLSGMVTEAGPEGWTQEDFTAYIHAVLELFGPERVMFGSDWPVCLMAATYDEVLQILRTALQERLSPEEMEPVFGANAVRFYKLNSL
>NZ_CP009280.1|WP_042135896.1|3113554_3114424_-|AraC-family-transcriptional-regulator
MEPIRKHFDNELPFSLLLDYKETKSPQRELPDHQHDWYEFIYVYGGKGTFFIDQTFYEMRQGDVIVVPGNTVHRGFPDKEEPVTSSAVFFSPGLVLNHTYSESYAYLKLFDAAKKNKQYKYTLSPEHAGILQNDIDVIHGEREQSRPDGGQALTLLLHLTLLHLNRYCLPQAAEPVTSSALLPDWFREALSYINDHLDQPLELSALAGRAAISPAHFSRVFKQRLGMNVTDYIATKRIFAAKDCLLQSSYTIEQIAMACGFESMPHFYRTFKKITKVTPAAYRRNSRTH
>NZ_CP009280.1|WP_042135894.1|3111098_3113543_+|DUF5110-domain-containing-protein
MKGGTIVNLIATHSGTDGVRLETTEGIMHIAMYTPGIARIRYTLNAELSGKESLMVVSRPEAESVEWTVEEHSGHLEISTVLLKIKVDKLTCAFSYWDADGRLLTREPSRGGKTLERTEVYHTVFDASADTVETGQGADGLRARAEGINRRLDREAFHTKLEFEWQEGEALYGLGSHEEGMMNLRGRQQYLYQQNMKAVVPVLVSTRGYGILVDSGSYMTFHDDAFGSYLWSDADEEMDYYFIYGPEFDQITGGIRYLTGDAPMLPKWSFGYVQSKERYISQAELIATVQEYRERSLPLDCIVLDWQSWTGNLWGQKTFDPERFPDPSQMMNSLHAMNAKLMVSIWPIMGAGGANHEEMKESGFLLGNQATYDAFREEARELYWKQANDGLFSHGVDAWWCDCTEPFEADWKGAVKPEPEQRLLINTSESKRYLDPGLINAYSMQHSKGIYEGQRAATSEKRVVNLTRSAFAGQHRYGTVTWSGDIAANWETLRKQIADGLNFCLTGSPYWTLDIGAFFVKKQKEQWFSNGDYDEGVADLGYRELYIRWFQLGAFLPMFRSHGTDTPREVWQFGEEGEPMYDTLVKYLKLRYRLMPYIYSLAGAVAHRSYTLFRALAFDYREDVQVHSISDQFMFGPAFMAAPVTEAMYYGPGSLELEGVRKLRSVYLPAGEWYDYWSDERIEGGQMIEAKAGLETLPLFVRAGSIVPLGPEIQYTDEQPDAVISLKVYGGKDVSFTLYEDEGDNYNYEHGSYSMILMTWSEAARSLTIGKRAGDYAGMQAVRQFTVEIAGQAGSCIVNYEGEAVTVREADLNL
>NZ_CP009280.1|WP_052421800.1|3110104_3110998_-|helix-turn-helix-transcriptional-regulator
MYEHRYRENKLHGQPEFPLHIYRVEHQARVHSILPVHWHNEMEIIYLAEGRATFQVESREFTIQAGDALIVHPGELHSGMDTVSGGTCYYSIVFKCSWLSSPYPDRVQSLFLDPLLQGTTRLPALLSAADDTHTPLLYLIKELLNRYEHQSAAYELSLKALLLLFIADSHQYRLTGQNPDPEPRHRREYNRQIREVLSYMEQHSRDRLELDQLASVVSLSRSHFCKFFKAQTGMRPMEYLNYIRISQAASLLRSGSYNVLEAALESGYQHVSYFSKWFRHYMNMTPSDYKARYSSGV
>NZ_CP009280.1|WP_042135892.1|3108537_3109965_+|family-43-glycosylhydrolase
MTQQQGFNPYLPSCEYIPDAEPYVFEGRVYVYGSHDRFNGHAFCLNDYACWSAPEDNLADWQYEGVIYRTTDDPLNPEGSMCLYAPDVTKGPDGRYYLYYVLDKVPVVSVAVCGKPGGKYEFYGYVTYGDGTRLGEREGDEPQFDPGVLTEGDTTYLYTGFCGYGDKSRHGAMATVLGPDMLTIIEEPVFVAPSQPYSGGTGFEGYEFFEAPSIRKRGDIYYLIYSSISMHELCYATSKHPTRDFVYQGVIVSNCDLHIDTYKPADQPMYYGGNNHGSIVEVNGEWYIFYHRHTNGTAFSRQGCIERIEFRADGTIPQVEMTSCGPNGGPLQGSGEYPAYLACHLFCKDQEMYTGGFGPIGAWMDSRFPKITQDGRDGDEETGYIANMTDSATAGFKYFKCEGVTRVSIKVRGYCHGEFEVKAAWDGPALGRIPVGFTNVWKEYTAEVAIPDGVQALYFTYTGNGGAQLASFTLK
>NZ_CP009280.1|WP_042135891.1|3107131_3108277_-|xylanase
MNFFTEGSFYTGKYRNLFLENGLEAEAISQRLEDTWNELFYGAPGVRIYHPMGDDKGYIVDTGNTDVRTEGMSYGMMMAVQMDKKEEFDRLWKFAKVYMQHTEGRYKDYFAWHCKLDGTRLSPGPAPDGEEFFAMALFFASARWGDGAEPFNYSGQARIILRACVHKGEDGEGDPMWDPATRLIKFIPETPFSDPSYHLPHFYDLFALQADEADRAFWKDAAAQSRAYLHKACHPETGLSPEYANYDGTPAEPQPHGDFRHFFSDAYRVAANIGLDYEWFRCDPWQVEQSNRIQAFFRDTKPEDYRRYTIDGQPFDELSLHPVGLLATLGMASLAADGPDAGPFVKLFWHTPLRTGERRYYDNCLYFFTMLALSGNYRIYR
>NZ_CP009280.1|WP_042135908.1|3121192_3122875_+|extracellular-solute-binding-protein
MHKTAKRSAKAAAAGVLALTLALTGCGSGNNSSNTGSKDNATGGNASPAAAGDDNAPVTFSVFMSGPGQQPTPDNKILKLMKEKTGVSFNMEFLVGDLQQKLGVMIAGGDYPDIMSGDDKLINAKAYIPLEDLIEKYAPNLKKHYADVWNQIKDESDGHIYVLPSYGVYQGKITEPTYQGPGFWLQKKVLEEMGYPTPKTLDEYFDIIAKYKEKHPDVIGFESLNFDWRVFPLQNAPEHLSGHPNDGAVVVDNNVAQIFADKDMSKDYYKKLNEINAQGLMDKEAFVQNYDQYLAKIASGKVVGMFDQHWNFQDGETSLISQGKIEDTYIGFPLLYPGAEEWYRDRGAVGTNRGFGISINAKDPERIIKFWDQMITEEWQKTIQWGVKGEDYEVNADGSFYRTPEQRANADKTSWQVANKITGMHGYMPKIQGTYSDGNAADPGTQPQEFFDSLKPYDQKILKAYNKKSWSEFFKEPKENHIYFPAYSIVLKDGSPAQLAQSKLNDLQVKFLPKAIMASPDEFEDVWQDYVDKIHKLDIKAYEDRINEGIQQRIEKWSVK
>NZ_CP009280.1|WP_052421801.1|3122968_3123955_+|sugar-ABC-transporter-permease
MSDAVLDKQVKKQKTRRSKVDPEIGVSLSWKTLKIQKQLIFMSVPIAIYLIIFNYVPVWGWIMAFQNYRPALSFGQQEWVGFQQFKFLFSDETFMLVLRNTVAMSFINLVLGTVTAIGLALLLNEIRLKFFKRIVQSISYLPHFLSWVIAAGIVATSLSIDDGIVNVILMKLHLIKDPIMWLSEGKYFWGIVGASNVWKEVGWGTIIYLAAITSIDPSLYEAASIDGATRLQKMRFVTLPGIKATFVILLIMNIGHILDAGFELQYLLGNGLTIDYSQTIDIFVIKYGISMGNYSLATAAGIFKTIVSVVLVFMANYTAKRLGEERLI
>NZ_CP009280.1|WP_042135910.1|3123969_3124881_+|carbohydrate-ABC-transporter-permease
MKAVAKGSSRIEPVVFHTLNTLFMLFVVAVTLYPFLHTMAVSFNDGSDTLAGGIYLWPRSWTLENYKAVFVSGTIYHAAFISVSRTVISTLLGVFLTTMLAYALAQPQYIFRKKIGLLFILTMYFNAGLIPNYFLIKNMGLLHSFMVYILPSLVSAFNLIIMRTYIRGLPFSLTESAKIDGAGDFRIFWKIIFPLCTPVLATVALFIAVGSWNAWFDTFLYASSDLKLSTLQYEMMKLLGSTMSTNNDPSMLAGGQNNQVQALVTPASIRSAITIVTAVPILFVYPFLQKYFVVGLNLGSVKE
>NZ_CP009280.1|WP_042135913.1|3125011_3126544_+|response-regulator-transcription-factor
MLKVLFADDEPLMLEGLRFLVDWEKLNFEVCGEALDGEDALELIHSTRPDLVITDVRMPVIDGLELIKRASKTDFRPKFIIFSGYADFEYAKRALKYGVSNYLTKPLDEKELTEALQIVTDQIHKERKVSSRREALSALMQADTVSRLLMRENTEEERQKGMKSLGITPASRICCILVHGTAPDSLQLREQVSAMGGKEPLRSLSVYPFTAGSGKHGYLLVSPQEGPELDPAMLTSWMDEIRPLYSTPVCFTASLQHHGPEALNSAYQDALAAELCRPDAAEGGAAGFFEKQDKTQMAMLPAELRRSLLQSVTEGKLEHLSGQLRDVFKIFSAEVASSSWIDAFLANIKAELLREITARGGDYAQWVKKWFPSRYTASCLPLLERQTEEELCEAAEWFAAAADGRREDQIVSAVTEYVRRHYQEKLKLQDIAKVLHVNSAYLGQRFRKHYGSSFNDYLHEYRIEEAKKLLRRTDMGISDISSRVGYADADVFAAKFKALNGVTPTVYKKS
>NZ_CP009280.1|WP_081969936.1|3126467_3128375_+|sensor-histidine-kinase
MRTLMCSLPSSRRSTALRLPYTRRAKSRGGGDCMKHKRKPSAFINDIPLKYKFLFIYLLCVLVPILSINALFYVQISRNVEVRERENLGISVDRVVYDLMQIVNECVAISNTVAADRPYMEMMDYAYPDNEAYYDAYNDFLKDKLRQYSNLHSYIYWMGIYTSNPTIQNGSSYFILSDKDKQSEWYRKISSSTDKVLLTSYQGTNPLNPPQQEVFVSLIRKLDNFTGQPYNKYLRIDLRLNNVQELFQKERDYLDFKLLDEKNRIVLASGQSFYSLDTNALLNVDTSLDQPSKQIVRTLSSAAYTKGWRLVGTPEGRKVNHEMVHALRISLILALLTIILPTLLMIVIIRSYNLRVRLLYKHMKLVKYEQFESIDMYEGKDEIGGLIRSFNLMTGKIRNLINDVYKLEIQKKDLELERVRAELKYLESQVDPHFLFNTLNAILVICKKYKYEQVTDVIRNLALIMRRLLSWKDDLITVEEEVSFIEMYLQIEKFRFQNRFSYVLDIEPEVLKCRIPKMSIQALVENSCKHGLQSVKWAREIHVSAARDNAGLLIVVTDNGKGIEKEKLEWIKSHLETEQDSGQNVGLRNVYKRLMLYYNGRARFSIESTEYEQTVITIRIPEDLSLDLVVEGSHV
>NZ_CP009280.1|WP_052421802.1|3128367_3129888_+|response-regulator
MYKVVLADDETLALEGLRTQTDWEELGFEICGACENGEEALAAIVQSSPDLVITDIRMPGIDGLELIRRVRSLEMEQPIFVVLSGYGEFEYARTAIRYGVSHYLLKPVVEAEWDKVLTDITDELELRVKQRMQQSMLASRLLPLAIARMLEGHWAEPEEEAAEQMDRLDETVTGWTYLHVEGDSSNITDLCRELAGPAGALFIDLPGDQAGLVVESSAGAAGLAEQLYAGLIRSGVKGSVSIGPSVQSLRELPVSYREAAGAAARHYFYSDGSGPVHSAIEGEGQVNYNLPATELLEEIISAVERLQEQKVQEKLNEMFSVFKENRTDPGVVQMTSMDIMLRSMELLKEFGGADDQWIGSLDFFRTEPKSLEALQATLQSALATSMNYIRQHKERNSEHPLIRVECFLRDHYSRHLTVKEIAEHFYINPVYLGQAFIKKHGISILEYIHNLRIEAAKKRLIETRDTVRSIVESVGYVHYHHFLREFEKRTALKPVAFREQSQSDKG
>NZ_CP009280.1|WP_042135917.1|3130347_3131778_+|family-43-glycosylhydrolase
MTTQLNQATGKVPPNGNPLVAHRYGADPYALVFGDRVYLYMTNDALEYDESGVVKENSYSSINTITVISSADLVNWTDHGAIAVAGPEGAAKWATQSWAPAAVHKVIGGKDKFFLYFANNASGIGVLSSDSPVGPWVDPIGEALILRSTPGVADVTWLFDPAVLVDDDGKGYIYFGGGVPEGQFAEPGTARVMRLGEDMTSVVGTAEVIPAPFMFEDAGIHKRNGVYYYTYCSNFYDGERPEGSPPAGEIAYMTSDSPMGPWTYQRTILKNPGHFFGVSGNNHHAVFEFHDSWYIAYHAQTLSKAQGIANGYRSTHLNRLTHLEDGSIQEIHADYEGVQQLVTLNPYERIPAATMGWSAGVKTEFLTAGGEQIVTDIENGGWIGLSGVDFGSRGAKAFQVSVLGLEAGGVLELHLDDPAGPLAGKLSVPAANGAEWTELKTEVHGAIGVHSLYLVFTGASGKDLFKLAAWKFTTEA
>NZ_CP009280.1|WP_042135919.1|3131801_3133316_+|glycosyl-hydrolase-43-family-protein
MNTAIITNPVMWADVPDVDVIRVGPVFYMVSTSMHSMPGCPIMKSENLYDWEIVNYVYGTFEDHEAHRLEDGQGIYGSGSWAASLRYKEGIYYVCFSSNDMDQFYIYRTGDIEHGPWERSVIPGLHHDPALLLDEDNRNYVIYGNGDIMLKELTADLTAVKPGGTDQLLLEGEREDIGLRIEGCHAHKRNGYYYLFFIEWPRTGNQRRRQLCYRSRELPGPYERKVILDDDLGYQNNGVAQGGIVDTPDGDWYAVLFQDHGAVGRIPCVLPVSWEQDWPVIGENGEAPKVFRTKLPAGEPKPLVISDEFDYTSGRLALNWQWNHNPDNGLWSLTERPGYLRLRTGRTADSILRARNTLTQRTEGPACSAETLIDLSGMQTGDKAGMVALQNGYGTVEAAALKQGGFSVNMCVNSGDGYPQTVESIPFTGNRIYLRIDFNFEDSVDQAHFFYSADGAVWKAIGGTLHMKYTLDHFMGYRIGLFNYATQSAGGYADFDYFRYRRQG
>NZ_CP009280.1|WP_042135921.1|3133522_3134314_-|AraC-family-transcriptional-regulator
MPTIHYVEYDAAHQHDFVYSIPEGLDAWLLVLTQTPALFEVNGELKEFPAHSAVLYPPKHSIYYRACSRKYVNDWVRFDADESYITETVLPVGTPFSLPDPGYCHQLFQLLTLENSFQNDYRELSIDYLFRLLFNKLSEASEDKLTPQYYNLLELRKTLYSNPGHPWTVSSMAGHLHISTGYLQTIYKSTFGISCMEDVIHCRIRLAKEKLGYGQHKIAEIAALCGYANVEHFCRQFRQLTGFSPRAYREKLASKQAETRQEE
>NZ_CP009280.1|WP_042135923.1|3134486_3136301_+|family-43-glycosylhydrolase
MIPQRNEDRNQILCYTRLPQEDMVYASRLAHSMHLAYSTDGLLFQELNHNSGVLFAKATENEDGTLRAKSLNHPYLFHLADGNYGVIAVRTEADGEADEQSKGKVLLFSSADLLQYSEVGLLELKADTFVSDVSCQYDTEQNGYLISWIDEYGQGYESWMTDIMSLKNVSAPEKAKPFTLDTVLADIEGILPRNVISVSAETARRLFFKLTVPENIAIVVPDRVSAASVEEVKAVRATALYSDGTQASKKVDWNIGAIDWSQAGTYRITGEIHQEHYPFPIALDRADPCIAQWKGKYYFIATNDADQNHTLYMREADTIPGLVTAEEVLILDSSTHEQIRGLLWAPEFHVIEDELYIFHAATSGEFFYEESHVMKLRAGGRPMNAADWTIPERVVKKDGTYLCEAGKTISLDMTVIRWNGKLYAAWSERQFVPVDLGAWVYIATINPQEPWKLTSDPVLLTRPDYGWANNHTFVDEGPFALYSDDKLYVTFASAAVDATYVVGLLTADKGADLLDIESWTKGNYPLLTSRSVPGEYGPGHNSYVTDEDGVIWNAYHARPGIDGPRSSGLRRVHFDIDGAPVLDLTEEKDLNPELKQVSMEVNVG

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_CP009280_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_10

3643229-3643366

Orphan

Consensus_repeat	Method
ATAACTGTATTCTGTACAATTAAAA	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP009280_10

>merge|NZ_CP009280|10|3643229-3643366|CRISPRCasFinder
ATAACTGTATTCTGTACAATTAAAAGGCGGAGAAAACCCGGATGTGCAGGAATAACTGTATTCTGTACAATTAAAATTGAGCAAAATATTCTTCTTCGGCAAAAAAGAATTATATAAGTGTACAGAGTGCAATTAAAA

>NZ_CP009280|10|8|3643229-3643366|CRISPRCasFinder
ATAACTGTATTCTGTACAATTAAAA	GGCGGAGAAAACCCGGATGTGCAGGA
ATAACTGTATTCTGTACAATTAAAA	TTGAGCAAAATATTCTTCTTCGGCAAAAAAGAATTAT
ATAAGTGTACAGAGTGCAATTAAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042136644.1\|3635366_3636530_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226669
NZ_CP009280.1\|WP_042136667.1\|3650780_3651281_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042136658.1\|3645466_3646066_+\|nitroreductase-family-protein	unknown	unknown	gnl\|CDD\|380317
NZ_CP009280.1\|WP_039298093.1\|3647935_3648271_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379842
NZ_CP009280.1\|WP_042136662.1\|3648470_3649577_+\|lactonase-family-protein	unknown	unknown	gnl\|CDD\|378416
NZ_CP009280.1\|WP_042136651.1\|3639872_3640217_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224647
NZ_CP009280.1\|WP_042136646.1\|3636680_3637349_+\|conjugal-transfer-protein-TraX	unknown	unknown	gnl\|CDD\|368639
NZ_CP009280.1\|WP_042136664.1\|3650067_3650748_+\|phosphatase-PAP2-family-protein	unknown	unknown	gnl\|CDD\|239486
NZ_CP009280.1\|WP_042136654.1\|3642819_3643194_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042136656.1\|3643531_3643747_-\|DNA-binding-protein	unknown	unknown	gnl\|CDD\|181104
NZ_CP009280.1\|WP_042136659.1\|3646437_3647682_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|234605
NZ_CP009280.1\|WP_042136649.1\|3639382_3639736_-\|DoxX-family-protein	unknown	unknown	gnl\|CDD\|379266
NZ_CP009280.1\|WP_039298097.1\|3649734_3649956_-\|RNA-chaperone-Hfq	unknown	unknown	gnl\|CDD\|379947
NZ_CP009280.1\|WP_052421842.1\|3637442_3638951_+\|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|377924
NZ_CP009280.1\|WP_039298089.1\|3646145_3646340_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227213
NZ_CP009280.1\|WP_042136652.1\|3640293_3641508_+\|chromate-transporter	unknown	unknown	gnl\|CDD\|273350
NZ_CP009280.1\|WP_042136642.1\|3633830_3635360_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|184134
NZ_CP009280.1\|WP_042141113.1\|3641786_3642716_+\|phosphotransferase	unknown	unknown	gnl\|CDD\|366736
NZ_CP009280.1\|WP_081969972.1\|3643776_3645189_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|380032
NZ_CP009280.1\|WP_042136647.1\|3639077_3639353_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042136644.1\|3635366_3636530_+\|sugar-ABC-transporter-permease	gnl\|CDD\|226669	COG4214, XylH, ABC-type xylose transport system, permease component [Carbohydrate transport and metabolism].	1.98346e-149
NZ_CP009280.1\|WP_042136658.1\|3645466_3646066_+\|nitroreductase-family-protein	gnl\|CDD\|380317	cd02140, Frm2-like, nitroreductase family protein. A subfamily of the nitroreductase family containing uncharacterized proteins that are similar to nitroreductase. 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. Members of this family are also called NADH dehydrogenase, oxygen-insensitive NAD(P)H nitrogenase or dihydropteridine reductase.	9.13304e-109
NZ_CP009280.1\|WP_039298093.1\|3647935_3648271_-\|hypothetical-protein	gnl\|CDD\|379842	pfam16409, DUF5017, Domain of unknown function (DUF5017). This family of proteins is functionally uncharacterized. This family is found in various Bacteroides and Prevotella species. Proteins in this family are around 350 amino acids in length.	0.0082688
NZ_CP009280.1\|WP_042136662.1\|3648470_3649577_+\|lactonase-family-protein	gnl\|CDD\|378416	pfam10282, Lactonase, Lactonase, 7-bladed beta-propeller. This entry contains bacterial 6-phosphogluconolactonases (6PGL)YbhE-type (EC:3.1.1.31) which hydrolyze 6-phosphogluconolactone to 6-phosphogluconate. The entry also contains the fungal muconate lactonising enzyme carboxy-cis,cis-muconate cyclase (EC:5.5.1.5) and muconate cycloisomerase (EC:5.5.1.1), which convert cis,cis-muconates to muconolactones and vice versa as part of the microbial beta-ketoadipate pathway. Structures of proteins in this family have revealed a 7-bladed beta-propeller fold.	5.41069e-117
NZ_CP009280.1\|WP_042136651.1\|3639872_3640217_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	4.20307e-36
NZ_CP009280.1\|WP_042136646.1\|3636680_3637349_+\|conjugal-transfer-protein-TraX	gnl\|CDD\|368639	pfam05857, TraX, TraX protein. This family consists of several bacterial TraX proteins. TraX is responsible for the amino-terminal acetylation of F-pilin subunits.	3.07401e-26
NZ_CP009280.1\|WP_042136664.1\|3650067_3650748_+\|phosphatase-PAP2-family-protein	gnl\|CDD\|239486	cd03392, PAP2_like_2, PAP2_like_2 proteins. PAP2 is a super-family of phosphatases and haloperoxidases. This subgroup, which is specific to bacteria, lacks functional characterization and may act as a membrane-associated lipid phosphatase.	2.07198e-53
NZ_CP009280.1\|WP_042136656.1\|3643531_3643747_-\|DNA-binding-protein	gnl\|CDD\|181104	PRK07758, PRK07758, hypothetical protein; Provisional.	8.18467e-15
NZ_CP009280.1\|WP_042136659.1\|3646437_3647682_-\|peptidylprolyl-isomerase	gnl\|CDD\|234605	PRK00059, prsA, peptidylprolyl isomerase; Provisional.	3.16336e-46
NZ_CP009280.1\|WP_042136649.1\|3639382_3639736_-\|DoxX-family-protein	gnl\|CDD\|379266	pfam13564, DoxX_2, DoxX-like family. This family of uncharacterized proteins are related to DoxX pfam07681.	3.23595e-14
NZ_CP009280.1\|WP_039298097.1\|3649734_3649956_-\|RNA-chaperone-Hfq	gnl\|CDD\|379947	pfam17209, Hfq, Hfq protein.	1.25072e-23
NZ_CP009280.1\|WP_052421842.1\|3637442_3638951_+\|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl\|CDD\|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	4.30785e-19
NZ_CP009280.1\|WP_039298089.1\|3646145_3646340_+\|hypothetical-protein	gnl\|CDD\|227213	COG4876, COG4876, Uncharacterized protein conserved in bacteria [Function unknown].	1.19821e-19
NZ_CP009280.1\|WP_042136652.1\|3640293_3641508_+\|chromate-transporter	gnl\|CDD\|273350	TIGR00937, Chromate_transport_protein, chromate transporter, chromate ion transporter (CHR) family. Members of this family probably act as chromate transporters, and are found in Pseudomonas aeruginosa, Alcaligenes eutrophus, Vibrio cholerae, Bacillus subtilis, Ochrobactrum tritici, cyanobacteria and archaea. The protein reduces chromate accumulation and is essential for chromate resistance. [Transport and binding proteins, Anions].	3.3623e-103
NZ_CP009280.1\|WP_042136642.1\|3633830_3635360_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|184134	PRK13549, PRK13549, xylose transporter ATP-binding subunit; Provisional.	0
NZ_CP009280.1\|WP_042141113.1\|3641786_3642716_+\|phosphotransferase	gnl\|CDD\|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	3.44046e-05
NZ_CP009280.1\|WP_081969972.1\|3643776_3645189_-\|metallophosphoesterase	gnl\|CDD\|380032	pfam17839, CNP_C_terminal, C-terminal domain of cyclic nucleotide phosphodiesterase. This is the C-temrinal domain found in Listeria monocytogenes, Lmo2642 cyclic nucleotide phosphodiesterase. The auxiliary C-terminal domain, consists of five alpha-helices forming a long helical bundle, and is connected to the catalytic domain pfam00149 by two loop segments. It is suggested that this auxiliary domain of Lmo2642 might confer functional specificity to the protein through the interactions with unknown factors or involving the substrate recognition.	1.50291e-27

>NZ_CP009280.1|WP_042136654.1|3642819_3643194_+|hypothetical-protein
MDKAKRELLMNICLISPVLSVLYGIMVTGIDNSLVSETTYISGPGGFVVFVLFFLILYPLHILLSIFQFAVIRFAGESLVKRLVISNATGLGVVGAIYYITQEIEALCLIFSLAVFSVAALISK
>NZ_CP009280.1|WP_042141113.1|3641786_3642716_+|phosphotransferase
MEKVFGTSYAVAMVTKLHGGAQKVVYKIDCTNGFSCVLYVWDITMNYFQEEIVNQNTNVQSYGSEQFEINNRYLLEQSIRTPALYDMNMDRNPYDFDYALIEYVTGQAAEAYFNHSDSRVKDTIFQRLGDMITGMHTGESDIYGKPDQTERSSGQCHLIQLQNAIIQLSYASEYIDVIRRNQGKLLDMLYKLESRVERRSRYGYIHGELGPNHVLVTDQLEPCLIDIEGAGFYDIEHEHSFMEFRFGDFYRYLKNDNLDVNRKLFYQYHHHLSLISAGLKLVQRGYPDQQTAKGISDYHTRRALQFIES
>NZ_CP009280.1|WP_042136652.1|3640293_3641508_+|chromate-transporter
MQTDEQRVPEDIQKGRAGALLEVLLVSAKLGLTSFGGPIAHLGYFHNEYIRRRKWMDERSYADLVALCQFLPGPASSQVGIGIGVVRAGLLGGVVAWLGFTLPSVIALVAFAFLLQGYDIGSAGWIHGLKIVAVAVVAHAILGMGQKLTPDRERVTIAVIGAAVTLSWQTAYSQVLTIAAAGIVGVWLYRKKTAEGTANLHVSISRTFAILCLLLFFGLLVALPLLRGTAETGGLAIFDSFYRSGSLVFGGGHVVLPLLEREVVPSGWVSQADFLAGYGATQAVPGPLFTFASYLGALTGGVTGAIVATSAIFLPAFLLVVGALPFWNSLRKNLKIQGALAGINAAVVGLLLAALYDPLWTSAIVEPMDFALAAILFIMLVFWKLPPWVVVVAGSAGGMLLGVY
>NZ_CP009280.1|WP_042136651.1|3639872_3640217_+|helix-turn-helix-transcriptional-regulator
MESYCKFESALDILIGKWKPVILLQLMNKGTMRFGELQKSIPDINKKMLTQQLRELEYNDIVHREVYNQIPPKVEYSISEYGKGLSSVLQVLNDWGVSHIEHMKKLYGVDRSGS
>NZ_CP009280.1|WP_042136649.1|3639382_3639736_-|DoxX-family-protein
MNTALWIVQGIAAAGFVYSGWLKAFRYGQAKKSWGWVSDVPKALVVFIGVAELLGALGLILPYALNIVPVLTPAAAAALAVTVLCGALFHIRRKEYREIGVNIFFIVLALIVAAGRF
>NZ_CP009280.1|WP_042136647.1|3639077_3639353_+|hypothetical-protein
MQRIILIYKQFLTEPLWFKILIITTLLAAVIFSSSSFPQNGYYQLTSKLAAAIFFTAYGVNFRSNTRVSAVFFVMAAVCVFLSWNIWMDHL
>NZ_CP009280.1|WP_052421842.1|3637442_3638951_+|copper-amine-oxidase-N-terminal-domain-containing-protein
MKKMKARTKWLVPFLALLLILAGCQTVGGFDVNKALLGDLDVKSSESSTTLSLSAVPAVGIRAEDQEIVDLINSLSLTLGSVKLQDNGNVSASGIVGYKQSKIPFSLFMDQANIVFTAEGAKQPFYFPIQGYEDTLGIEGLDQTKTLELSKLISQFVVKNLPNPGAITVASVSESVYGQQTSLTKLHTEITGEELPVLLKSFLRSISKDTEGFTALISGLYDYLYPLLEASGEDLNSLGFGEIPLDDKEGVVTVAHDAAKLAVDALLLVYDKQLENLYESTPELKTVLGKDTKLTVDLFVDSGFHVRKQNIDLKVALPASEDLPLQSINVKLVSETWNVNGPVTADPISTTGGIDFSSAQLTPGETLRSFEQGSAVYNLLKDDMGITSKSLMMAPDDDYYYPIVDNGTTYVPLRYIAEDLDASVEWDAANRAINVTDDVYGDLLVFKIGSAQAQIAGATVKLPQPVFVDEYGDAYVPLRVLAQGLHATVEVDEDGYIWIDRP
>NZ_CP009280.1|WP_042136646.1|3636680_3637349_+|conjugal-transfer-protein-TraX
MQIIAMLTMLIDHIGYIFFPGELAWRVVGRIAFPIYCYALVQGHIHTSSRPRYLRRLLVIALLAQIPYNLALDPGGWNVVFTLLLSAAVLTLLDKLPKLWYGIPVIILAVLLMDILPLDYNAYGLLLVLIFRYTRSYWLVLAHFALNLFYLFYYNWLVQMASIVPTILIALTPGFWILLERKRLPRWVWWSFYPGHLAVLALVKILFFQDWVSIEWRSLFTL
>NZ_CP009280.1|WP_042136644.1|3635366_3636530_+|sugar-ABC-transporter-permease
MGAITELFKKNIRQYGMIIALIFISIFFQIMTDGILLKPLNVTNLILQNSYILVLAIGMVLVIITGHIDLSVGSVAAFIGALSAIMMVDMKMNPVLAVILSLLMGALVGAWQGFWVAYIKIPAFIVTLAGMLLFRGLTMIVLNGQSIAPFPKAFQKISSGFLPDIAGGSSLNVLTLVIGVILSVLVVYQEYRSRQITLKYGFEQSPVWISVGKAAALVIVINLFTYVIAQYNGIPNILVILLVLIAIYSFVMNHMTMGRHIYALGGNEKAASLSGVKTKRVTFWVFVNMGVLAALSGLVFAARLNSATPKAGTNFELDAIAACFIGGASASGGIGTVVGAIIGGLVMGVMNNGMSLVGLGVDWQQGIKGLVLLLAVGFDIYNKSKTA
>NZ_CP009280.1|WP_042136642.1|3633830_3635360_+|ATP-binding-cassette-domain-containing-protein
MSEYILEMKGITKTFPGVKALANVNLQVKAGEIHALCGENGAGKSTLMKVLSGVYPHGTYEGDILYQGQVCQFKDIKDSEGLGIVIIHQELALIPYLSISENIFLGNEQARRGVINWNETTVKTKELLTTVGLKESPFTGVSTIGVGKQQLVEIAKALSKEVKLLILDEPTAALNEDDSENLLLLILELKKRGISSIIISHKLNEIEKIADSVTILRDGQTIKTLDMKRDAVTEDVIIKGMVGRDLTNRYPERTPELGETIFEIRNWEVYHPTQQDRKMLDQINLHIRRGEVVGIAGLMGAGRTELAMSVFGKSYGKRISGQTFMHGREVHLNNITQAIESGLAYVTEDRKQYGLILIDDIKRNISLSNLKKLSRRGVINENEEVLVAEEYRKKLNIKTPSILQKTVNLSGGNQQKVVLSKWIYAQPDILILDEPTRGIDVGAKYEIYSIINGLAAEGKGVLVISSELPEIIGMCDRIYTMCEGRISGEVERKDASQELLMKFMTRSRG
>NZ_CP009280.1|WP_042136656.1|3643531_3643747_-|DNA-binding-protein
MADTHESPPGSSLPEIISKPAHRALAGAGIVNLEQLTTITEAELLKLHGMGPKGIRILRQALADKGLDFAK
>NZ_CP009280.1|WP_081969972.1|3643776_3645189_-|metallophosphoesterase
MSSPLKDGTKRTMKFTLLILLSSALILSGCKDTASTSLNAAAAVTEPETAIDSTAPVSFWVATDTHYLDKALEDGGQAFQTYVTGGDGKMLPYSDELTEALVYDVEQKKPGFLILSGDLTNNGEASSHKELAAKLHRIEAMGTSVYVIPGNHDINNPWARSFDGDKQVVADHINVEDFLATYEDFGYHEALSRDADSLSYVVKAAPGLWLLMIDSAQYAHNEEYNFPQTDGRILPSTLSWMDENVKLAAQEHASIITVMHHNLLSHTSMAVSGFKLNNSQETMKTLRKDGLNLVLSGHIHMQDIRRDPAEDSIDPAMPVYDIATSAMAVNPHQYGAMTFDPVSRAFTYNTAAVDVEGWAQAKDITDPHLLNFKSYAEDTFAGESYEKAMTRLKDSTFTEAQKQSMAEVMSKLNVKYFAGTAADSLDEIQAMPGYKLWESMEGGFMSGYIRSMAEHSGQSNVSLEMVLTTQ
>NZ_CP009280.1|WP_042136658.1|3645466_3646066_+|nitroreductase-family-protein
MSKNFFEAVKGRRSVYAISKESPISDEQIQKIVEEAVLHSPTSFNSQSSRAVVLLGEQHDKLWDITAETLRKIVPTEQFEGTAQKLASFKAGYGSVLFFEDQAVVKHLQENFALYAENFPIWANQSSGILQFVVWTAFAEQGLGASLQHYNPLIDDEVKETFGIPAEWKLIAQLPFGTIVTPPGEKEFQPIEERVKVIK
>NZ_CP009280.1|WP_039298089.1|3646145_3646340_+|hypothetical-protein
MPWNKGDYPDSLKNFTAPVRNKAVEIANALLEDGYEEGRAIAIATAQAKEWGENHDKQIRKKNH
>NZ_CP009280.1|WP_042136659.1|3646437_3647682_-|peptidylprolyl-isomerase
MDKKDFNENGQLENGGTPPEENDTSVVTPEDGIERAEAVSEPQAEVIIPAEPVQAATESSSSVHSPKIEESVPVMNKVGDGTPPSKPAAPAGGKGWMIASIILAAALIVVLIVQPFKKDDSKIAVATVNGTDITKAQLYDKLVEAGGESTLQNLITTTLVDQEAKKANITVTDEDINQEIADLTTQFGGEEALNSALQQSSMTLDDLKKQMPLQVEIRKLVEPKVTITDEDISKYYDENKATFNQEEEVRASHILVETKEEADAIVKQLKDGADFAILAKEKSADTGSKDKGGDLDFFKRADMVAEFSDAAFNMKVGETSGAVKTDYGYHIIKVTDRKEAHEYTLAEKKEEITKTLKAQKVSEMSSTWLADLTKNATITNTLTDTPDASATPAASAAPDASADPAAAATEAPAK
>NZ_CP009280.1|WP_039298093.1|3647935_3648271_-|hypothetical-protein
MSSLLEARNVYEDFEVETDILFFKVGDHDLVIFHGRNYNIKKRMTAEQLNRLLSSNSYYHVYGGCYVNLNKISSIEDDCIYFGEMGLYAKSVRVPRRKQESIRHLLRGLSS
>NZ_CP009280.1|WP_042136662.1|3648470_3649577_+|lactonase-family-protein
MNENTKLLLFTGSYATAEESGVQVFAFDGEAGGTLERLDTADGITNPTFVNVDPSGLKLYAIGEKPSGEGGKEGEIVTFAIEPKTGKLTELKRTPTMPAAGTGQTTTCNINRDAESEHIVVCSYHGGTVGLLTLDADGIPEALTDIAVHTGHSDLPGHDRPHPHSAIFSPDERFLFVSDLGLDLIRTYRINKEAKKLEALGDTVLHEGAGPRHFVFHPDGKSAYVINELDSTVTSFLYDADAGTLQTAFTVSTLPEGYPSENNSCAEIAFSKDGRYLYGSNRGHDSIVVYAVNPASAELTLVEHVSTRGGHPRHFTVTPDGAYLIVANRDGNNLVVFSLDAAGGRLTFTGNTAELSKPVCVMPAVFAG
>NZ_CP009280.1|WP_039298097.1|3649734_3649956_-|RNA-chaperone-Hfq
MESLKLQERLLNQCISTKVPVTIFTTNGVKMQGLVTSYDAYTITLQGQGDGRQNVLFKSAVSTVVPLKPVSLK
>NZ_CP009280.1|WP_042136664.1|3650067_3650748_+|phosphatase-PAP2-family-protein
MLYYHYWSGGFRRFIWFLLGFILIAVLVKQGGAAGFDRAVIHIVQSVESPPLTALAKSLSLVGSSRLAIGISLLTMTILFFALKHRMELALFLWVGLGSQLLNTLLKLWFHRERPSIHRLIEQAGYSFPSGHSMAAFSLYGVIAYLLWRHMHNRRERFILILFTVLMTGGIGWSRIYLGVHYPSDVIGGYAASGAWLMLSAACFEAYRNSRERKGGGPQRKKDARK
>NZ_CP009280.1|WP_042136667.1|3650780_3651281_-|hypothetical-protein
MNNPIQRITAFTAAVMLTMAPAAAFAENPSAGTATSAPDSIHAGREHGHPHGGNKNFRAGGHFIINETAKLLEMDRSELIDSLKAGKTLSALAQEKKGWSEDQYIQKLSEAASLKVDESVKDGRITKEDADKLKAGLPVMIKLSLSRAAQFHQAKPSQQPAAPKTR

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_CP009280_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_11

4547993-4548077

Orphan

Consensus_repeat	Method
AGTTTTGTCAGCATCCGCTTCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_11

>merge|NZ_CP009280|11|4547993-4548077|CRISPRCasFinder
AGTTTTGTCAGCATCCGCTTCTTGCATCACCTTCGCAAAACTTGCTTCGAAAGCATACACTTAGTTTTGTCAGCATCCGCTTCTT

>NZ_CP009280|11|9|4547993-4548077|CRISPRCasFinder
AGTTTTGTCAGCATCCGCTTCTT	GCATCACCTTCGCAAAACTTGCTTCGAAAGCATACACTT
AGTTTTGTCAGCATCCGCTTCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_081970030.1\|4557187_4557616_-\|VOC-family-protein	unknown	unknown	gnl\|CDD\|366361
NZ_CP009280.1\|WP_042137725.1\|4555826_4556645_-\|VanW-family-protein	unknown	unknown	gnl\|CDD\|377286
NZ_CP009280.1\|WP_052421902.1\|4556641_4557166_-\|cysteine-hydrolase	unknown	unknown	gnl\|CDD\|238496
NZ_CP009280.1\|WP_042137702.1\|4538336_4539683_+\|ATP-synthase-subunit-J	unknown	unknown	gnl\|CDD\|273349
NZ_CP009280.1\|WP_042137719.1\|4552627_4553464_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379312
NZ_CP009280.1\|WP_042137712.1\|4545867_4546425_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042141238.1\|4543576_4544224_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042137714.1\|4548083_4548980_-\|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl\|CDD\|223654
NZ_CP009280.1\|WP_042137722.1\|4553529_4554444_-\|DMT-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP009280.1\|WP_042137708.1\|4544293_4544878_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379115
NZ_CP009280.1\|WP_042137717.1\|4549980_4550928_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein	unknown	unknown	gnl\|CDD\|270371
NZ_CP009280.1\|WP_042137724.1\|4554601_4555738_-\|glutathione-dependent-formaldehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|176243
NZ_CP009280.1\|WP_042137706.1\|4541555_4542785_+\|aminopeptidase	unknown	unknown	gnl\|CDD\|376723
NZ_CP009280.1\|WP_039298909.1\|4548976_4549879_-\|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl\|CDD\|223646
NZ_CP009280.1\|WP_042137704.1\|4540263_4541502_+\|aminopeptidase	unknown	unknown	gnl\|CDD\|376723
NZ_CP009280.1\|WP_039298880.1\|4539815_4540097_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_039298903.1\|4547198_4547975_-\|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224042
NZ_CP009280.1\|WP_042137710.1\|4544870_4545599_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293807
NZ_CP009280.1\|WP_052421901.1\|4551188_4552118_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP009280.1\|WP_156118649.1\|4543226_4543400_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_081970030.1\|4557187_4557616_-\|VOC-family-protein	gnl\|CDD\|366361	pfam00903, Glyoxalase, Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily.	1.19988e-12
NZ_CP009280.1\|WP_042137725.1\|4555826_4556645_-\|VanW-family-protein	gnl\|CDD\|377286	pfam04294, VanW, VanW like protein. Family members include vancomycin resistance protein W (VanW). Genes encoding members of this family have been found in vancomycin resistance gene clusters vanB and vanG. The function of VanW is unknown.	5.24663e-60
NZ_CP009280.1\|WP_042137702.1\|4538336_4539683_+\|ATP-synthase-subunit-J	gnl\|CDD\|273349	TIGR00933, Trk_system_potassium_uptake_protein_trkH., potassium uptake protein, TrkH family. The proteins of the Trk family are derived from Gram-negative and Gram-positive bacteria, yeast and wheat. The proteins of E. coli K12 TrkH and TrkG as well as several yeast proteins have been functionally characterized.The E. coli TrkH and TrkG proteins are complexed to two peripheral membrane proteins, TrkA, an NAD-binding protein, and TrkE, an ATP-binding protein. This complex forms the potassium uptake system. [Transport and binding proteins, Cations and iron carrying compounds].	2.3656e-98
NZ_CP009280.1\|WP_042137719.1\|4552627_4553464_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	7.50117e-13
NZ_CP009280.1\|WP_052421902.1\|4556641_4557166_-\|cysteine-hydrolase	gnl\|CDD\|238496	cd01014, nicotinamidase_related, Nicotinamidase_ related amidohydrolases. Cysteine hydrolases of unknown function that share the catalytic triad with other amidohydrolases, like nicotinamidase, which converts nicotinamide to nicotinic acid and ammonia.	2.4817e-55
NZ_CP009280.1\|WP_042137710.1\|4544870_4545599_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293807	cd07721, yflN-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis yflN; MBL-fold metallo hydrolase domain. This subgroup includes the uncharacterized Bacillus subtilis yflN protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	1.34045e-68
NZ_CP009280.1\|WP_042137714.1\|4548083_4548980_-\|phosphate-ABC-transporter-permease-PstA	gnl\|CDD\|223654	COG0581, PstA, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	2.69332e-94
NZ_CP009280.1\|WP_042137708.1\|4544293_4544878_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|379115	pfam13305, WHG, WHG domain. This presumed domain is around 80 amino acids in length. It is found to the C-terminus of a DNA-binding helix-turn-helix domain. This domain may be involved in binding to an as yet unknown ligand that allows a transcriptional regulation response to that molecule. The domain is named WHG after three conserved residues near the C-terminus of the domain.	1.25052e-19
NZ_CP009280.1\|WP_042137717.1\|4549980_4550928_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein	gnl\|CDD\|270371	cd13653, PBP2_phosphate_like_1, Substrate binding domain of putative ABC-type phosphate transporter, a member of the type 2 periplasmic binding fold superfamily. This subfamily contains uncharacterized phosphate binding domains found in PstS proteins that serve as initial receptors in the ABC transport of phosphate in eubacteria and archaea. After binding the ligand, PstS interacts 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. The PstS 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.	5.56e-91
NZ_CP009280.1\|WP_042137724.1\|4554601_4555738_-\|glutathione-dependent-formaldehyde-dehydrogenase	gnl\|CDD\|176243	cd08283, FDH_like_1, Glutathione-dependent formaldehyde dehydrogenase related proteins, child 1. Members identified as glutathione-dependent formaldehyde dehydrogenase(FDH), a member of the zinc-dependent/medium chain alcohol dehydrogenase family. FDH converts formaldehyde and NAD(P) to formate and NAD(P)H. The initial step in this process the spontaneous formation of a S-(hydroxymethyl)glutathione adduct from formaldehyde and glutathione, followed by FDH-mediated oxidation (and detoxification) of the adduct to S-formylglutathione. MDH family uses NAD(H) as a cofactor in the interconversion of alcohols and aldehydes, or ketones. Like many zinc-dependent alcohol dehydrogenases (ADH) of the medium chain alcohol dehydrogenase/reductase family (MDR), these FDHs form dimers, with 4 zinc ions per dimer. The medium chain alcohol dehydrogenase family (MDR) has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The N-terminal region typically has an all-beta catalytic domain. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit.	0
NZ_CP009280.1\|WP_042137706.1\|4541555_4542785_+\|aminopeptidase	gnl\|CDD\|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_CP009280.1\|WP_039298909.1\|4548976_4549879_-\|phosphate-ABC-transporter-permease-subunit-PstC	gnl\|CDD\|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	1.58685e-92
NZ_CP009280.1\|WP_042137704.1\|4540263_4541502_+\|aminopeptidase	gnl\|CDD\|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_CP009280.1\|WP_052421901.1\|4551188_4552118_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	1.36826e-40
NZ_CP009280.1\|WP_039298903.1\|4547198_4547975_-\|phosphate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224042	COG1117, PstB, ABC-type phosphate transport system, ATPase component [Inorganic ion transport and metabolism].	2.95385e-168
NZ_CP009280.1\|WP_042137722.1\|4553529_4554444_-\|DMT-family-transporter	gnl\|CDD\|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	6.27677e-17

>NZ_CP009280.1|WP_039298903.1|4547198_4547975_-|phosphate-ABC-transporter-ATP-binding-protein
MGIAEPVVRESFQTEDLSIFYGTYEAVKGISLPFAQNTVTALIGPSGCGKSTFLRSLNRMNDDISGSTTKGSIWIDGIDINASGTDVIKLRQKIGMVWQKPNPFYKSIYDNIAFGPKYHGIKGKKALDEIVESSLRRAALWDEVKDRLKDSALALSGGQQQRLCIARALSVNPQILLLDEPASALDPVSTGKVEELIKELKEELRIVIVTHNMQQAARISDYTAYFYLGSLVEYDKTEKVFSNPENQMTQEYIMGRFG
>NZ_CP009280.1|WP_042137712.1|4545867_4546425_-|hypothetical-protein
MYRKLRYASVVNKFLWNLKQVRLKDECVFVSGIPQNPQKSEAWKIKGINPSDSAESGRYEEIKGINPSDSAESGRYEEIKGINPSDSSESGWYEEIKGINPPESARSGRQAGMRGKSAPESAKSGWQAGMKSISAPESARSGRQAGMRGKSAPESAKSGWQAGMKSISALDFTRFCPGSSQNRAI
>NZ_CP009280.1|WP_042137710.1|4544870_4545599_-|MBL-fold-metallo-hydrolase
MRVTQEGYLHQLTWLPRLFPVNCYLVEEEEELTLIDAGMPYSLQGILQQSARLQKPLTRIVLTHGHMDHVGALDALKKLVPEAKVYISERDAALLAGDRSLRAGELQTPIKGSVPSKIATKPDVLLYEGDTIGSLTAISTPGHTPGSMSFRDQRSGALIVGDAFQTFRATAVSGKKVPLFPFPAMATWSLEQALASAYKLIDLVPSVLAVGHGNLVRHPVESMKHAAAEAGRVLVNGGKVHG
>NZ_CP009280.1|WP_042137708.1|4544293_4544878_-|TetR/AcrR-family-transcriptional-regulator
MARAGLDTHTLVLAAAELADEQGVQEVTLAALAAKLGVRPPSLYNHINGLAGLRTLLAIHGLEQLYDAMSAAAEGARGEQAVYALSQAYIGFARQHPGLYETTLRAPEQGDTALEAAGGKVLSLIIQVLSCFGLDEEGNLHAVRGLRSILHGFSALENQGGFGMPLDLNVSLTRLIRAYIAGIRCMGEGADELE
>NZ_CP009280.1|WP_042141238.1|4543576_4544224_-|hypothetical-protein
MAEVVAKLGIVPLAPLIPGHPSVNGLTLAENWHTGSELDPWGWRVRFPGEGLAGYGKFIKKKAVLVSREWLPAYLAAAGSPRSLEERYDSGLATREALTLLQIIREHEGIETRQLRSMADMKAKEKKTAFDNAVTELQGTLDIVISGVKQRLNADGEPNGWNSTSFETSGHWMNEAGIESFEGTREEAVAWLRSRMDGSWTPEAIAWISKALGWK
>NZ_CP009280.1|WP_156118649.1|4543226_4543400_+|hypothetical-protein
MKESFNQEVDSTEPERLEVQAPKDLSIVASDAIKYTAYIMLLFGFLYFLIAYLAPML
>NZ_CP009280.1|WP_042137706.1|4541555_4542785_+|aminopeptidase
MLDFKQKLENYALLAVKIGVNIQPGQTLVVNADIVSAELVRLIVRQAYEAGAKLVKVNYTDEFVTRTRYDLAPSESFLEPPKWQADELEDLARNGAAFLTIISANPDLLSGVEPSRISDNQKTAGQAMAPYREMMMANHVSWSGIAFPSPSWAAKVFPDAAPEQQIELLWDAIFKAVRADQENPVAAWSSHLGGLKQRCDLLNAKKYRKLHYTAPGTDLTIELPEGHIWCQAGAVNSRGMSFLANIPTEEVFTAPLKTGASGKVSSTKPLSYGGNIIDRFTLTLENGKVTDFTAEVGQEALASLLAMDEGAAYFGEVALVPFHSPISESGILYYTTLYDENASCHLALGAAYAFTLQDGINMTKEQLAERGMNQSLTHVDFMMGSLEMSIDGIADDGSVDPIFRNGDWA
>NZ_CP009280.1|WP_042137704.1|4540263_4541502_+|aminopeptidase
MTQTELQSKLSKYADLAVQIGVNVQPGQILVVNAPISAAEFVHLITAKAYAIGASQVKVNWSDEFITRQQFEHASPEVFTKAPTWYAGEVTEFAENGAAFLNVIAENPDALKGIDPERIANFQKTRGAALTKYREMQMSDKVSWSIVAIPSQPWADKVFPDVPEEERVDKLWEAIFHTVRLDREDPVAAWQEHLDTLEQKADVLNAKKYKSLHYIAPGTDLSIELPEGHIWAQGDSINAKGHSFVANMPTEEVFTAPKKTGVNGTVRSTKPLSYGGNIIDGFSITFEQGRIISVSAEQGQEALEYLISLDEGAKYLGEVALVPHNSPISDSNILYFNTLFDENASNHLAIGTAYAFCLEGGKEMNQDELIAHGLNTSVTHVDFMIGSAEMDIYGITADGTREPVFLKGNWAF
>NZ_CP009280.1|WP_039298880.1|4539815_4540097_-|hypothetical-protein
MNLEITKAEMKRVEDRSFVGRTVFTLENHSSPYEITFFSSRGTEWDYSLSFAGEPGSEEQFLEVDALLENDDDVYNQLLDAALDTQEIPEEEA
>NZ_CP009280.1|WP_042137702.1|4538336_4539683_+|ATP-synthase-subunit-J
MANLSFGYLRLTPPKILSLGFAILIAAGTLLLCLPAASTGGRISFIDALFMATSATCVTGLAVIDTGTQLTAFGQIVLLVLFQFGGLGFVTMATLITLVLNKRISLKERLLLQESMNQNSMQGIVKLIRRVLIYSLVIQLTGAILLAARFMMDMPFGKAAYYGVFHSISIFNNAGFDLFGDVHGPFSGLTRYVEDPIVNITSMLLIFLGGIGFIVLSDVIDFPKRKRLTLHSKVVLTTSAALIVIGAAIFFWLELNSTLKPLHAGGKIMASFLQAITPRSGGVTTIEIPLLRESTQFLMILLMFIGAAPGSTGGGIKITTFAILASTAYAKLRGKEDIVMFRHRISKENVYRAITMTLLSLMLVVISTMLLSVTESADFLTVLFEAVSAFGTSGITMGLTTELTTIGKVLVIILMFVGRTGPLTLAYALKPKNSKELYRYPEGNITIG
>NZ_CP009280.1|WP_042137714.1|4548083_4548980_-|phosphate-ABC-transporter-permease-PstA
MKPRTADKIATAIIVTFALLIVAILVGLLGYILIRGMSHISWDFLTSAPQKIRAGGGVGPQLFNSLFLLVLTLIITIPLGLGAGIFMAEYARPGRLTNFIRLVVEVLSSFPSIIVGLFGLLLIVNTFNLGFSLISGALALTFFNLPLMVRITEQAFRTVPKQQKEAGFALGLSKWKIVTSVLLPVALPTIITGTILSAGRVFGEAAALMFTAGMSSPRLDFSNWNPLSPSSPLNPFRPAETLAVHIWKVNSEGLAPDALQIAAGASAVLVLTVLIFNLAARYFGRFIYRKLTASKRMN
>NZ_CP009280.1|WP_039298909.1|4548976_4549879_-|phosphate-ABC-transporter-permease-subunit-PstC
MRVKPKKTRFEKHHIENFIGRAYMSFCVLLLIVIIVSMVYFVASKGIANFVSGEVKVSDFLFGTKWSPEADTPSYGAFPFIAGSFLVTLLAALIASPLSICAALFMTEIVPGWGKKLLQPVIELLSGIPSVVYGFVGLSVIVPFLRNTLPGQGIGVAAGALVLSVMILPTITSVAADALASLPQNLKESSFALGATRWQTISRVILPTTFPAIMTGVVLGMARAFGEALAVQMVIGNAPFVPRSLFESASTLTSVITLGMGNTTMGSPQNNALWSMALVLMLMTFVFVLLVRMLERRNKI
>NZ_CP009280.1|WP_042137717.1|4549980_4550928_-|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein
MQFRKSWIMALALTSVVALSACGNGGNNAATNNGGNAAATNTQNSSGAELSGSILASGSTALQPLVEQAAEKFMDANAGVDIQVQGGGSGTGLTQVAEKQVDIGNSDVFAEEKLKDADAEKAAALVDHQVAVVAIAAVSNPDAGVDTLTKQQLVDIFTGKIKNWSEVGGADQAIQIINRPASSGTRATFESFALGTKTDDLPGSIQEDSSGTVKKIIGETPGAIGYLALSYLDDSVKTLSYDGVEPSVDNVISGKYPVWAYEHMYTNGEPNETVKAFLDFMMTDEVQTGDVVELGYIPASQMQVSRDVAGTVTTK
>NZ_CP009280.1|WP_052421901.1|4551188_4552118_+|LysR-family-transcriptional-regulator
MNFVKLQIVVLIEKYKKVTDVAAEMGLKQPTVSFHMKSLESELGASLFQFRSGRVLLTDAGRALYQYAVRIVSLTAEAERTVKQFTSLASGNLELTASDIPGNYLVPKLLSQFTGLHDGIDVFLSILPDDAVRERLRSREIQLAVLHSADGQDDSFHTQVIARDETVLIFAPGHPFAGAQEITVETAAREPWVQHEAASFLRGISDKWTQLNHVKVWNHAVLSSPEAVKRMISGGGMVGVFSKSGIEAEVAAGSLAYAPLPGLHPGDGAFVLAWRKDYTLSPLQKAFAGMAGSDGLQEEDQREDLISSE
>NZ_CP009280.1|WP_042137719.1|4552627_4553464_-|methyltransferase-domain-containing-protein
MNEQDQNEPSGLNGGAAPSSEELWNEDTYAAWTSRFGSPAEAAEKLVKDPAGKLFPLNAYMGDVQGRKIMNLMGSNGMKAVALGLMGAEVTVADFSEANGRYATELAQEAGVKLNYIVSDVLGLPEAVLDGSYDLVFAEMGIVHYFTDLAPFMTTAYRLLAPGGKFVLRDFHPVTTKLISSKGSTAKVRKHKVNGDYFDTALEEKQVSYSKYMPSSGKAAGADRPNVVYWRRWTLGEIVTAAAASGLVIQELVEEPNLSSDVYDKGIPKTFTLVAGKR
>NZ_CP009280.1|WP_042137722.1|4553529_4554444_-|DMT-family-transporter
MIPKKPPVPVPLLMVIGIVAISFSSIFIKWSSAPVSVQGMYRLLFTSLLMLPFARRYSGAAWALRLKDWLLLGASGVMLALHFLLWMGSLNYTSVASSTMIMALEPLFIMLGAYILYKERNSASAMLGMAIAIFGVVFIGWGDIGLSAENLKGDMLSVGGTVAVAAHLLIGQKLVARMPSYLYSLIVFISAAIVFAVYNLVTSIPFFAYPAREWGIFVLLAVVPTVFGHILFNWLLQYASATTVSMNILGEPVGASILAFLLLGEQLSGLQWTGGVLVMAGLGVYLYSGRRKALKLQEALPNAS
>NZ_CP009280.1|WP_042137724.1|4554601_4555738_-|glutathione-dependent-formaldehyde-dehydrogenase
MKAVTYQGKKKVEVKEVADARLEKKDDIIVRITSTAICGSDLHIYNGEIPGMHDDYIIGHEPMGIVEDVGPEVTKVKKGDRVIIPFNVACGQCFFCQHEMESQCDHANEAKDTGGYLGYSDTYGGFAGGQAELLRVPYGNFGPFVVPEDAEMEDEKLLFLSDIVPTAWWGVENAGVKPGDTVIVLGCGPVGLLTQKFAWMKGASRVIAVDHIPYRLQHAKQTNNVEIFNFEKIKEFEKHMKEITRGGADVVIDCVGLDAKKTVVEKVETTLMLQGGSLGAFRIASEVVRKFGTIQLVGVYGLNYNMFPLGHLFERNITLKMGQAPVIHYMPALYRMIKENKFDPTDIITHRLPISRAEHGYKVFQEKEEDCIKVVLKP
>NZ_CP009280.1|WP_042137725.1|4555826_4556645_-|VanW-family-protein
MNPVITAMKPIRRSRLRLFAGKRYFIWKRYWKWITARGRLAKELRPEALPYEAASHATPLLRSLRNVDMQLQYNKITNLRLAVAKLDGLVIRPGETFSYWRSIGKPTRRKGYLDGMVLHYGGFRSGTGGGLCQLSNLIYWMALHTPLTVTERHRHSYDVFPDEQRTQPFGSGATCSYNYLDLQLRNDTEYTYQLKLHLDETHLHGEWRCDSRQLYNYEVYEDGHVISLEPWGGYVRSNAIRRRVLTHTGELAGDEAVAENHALMMYSPLLHG
>NZ_CP009280.1|WP_052421902.1|4556641_4557166_-|cysteine-hydrolase
MSTALLIIDVQEAMFAYPDMKLFDEEGVLERISSLLDKARLAGVPVIYIQHTEEEGEFVKGIPTWEISSRIAPQAGEKVIEKTTPDSFHLTGLQEELERLGVTELVICGMQTDYCVNATSRRAHSLGYSSVLVKDAHSTFDDNHLTGEEIVKQHNDALGSGIAALRSEQEVTFR
>NZ_CP009280.1|WP_081970030.1|4557187_4557616_-|VOC-family-protein
MVTASGGGNEMEFKSPQINLYVTDLARSRTFYEKLGFKLTFTAEIEGEAVHHELVLDGFKLGLASRTSANKVHGLTPGTNTGSELALWTEDTDLALQYLLENGGTLLSAAHDFLNDLRSAWINDPDGNPVQLVCRRKSAAGE

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_CP009280_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_12

4622784-4622887

Orphan

Consensus_repeat	Method
GTGCGATGAAATCTCAAGGTGAATAGGCTCACAAAACTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_12

>merge|NZ_CP009280|12|4622784-4622887|CRISPRCasFinder
GTGCGATGAAATCTCAAGGTGAATAGGCTCACAAAACTTAGGCGTATGCTTTCGAAGCGAGTTTTGTGCGATGTAATCTCAAGGTGAATAGGCTCACAAAACTT

>NZ_CP009280|12|10|4622784-4622887|CRISPRCasFinder
GTGCGATGAAATCTCAAGGTGAATAGGCTCACAAAACTT	AGGCGTATGCTTTCGAAGCGAGTTTT
GTGCGATGTAATCTCAAGGTGAATAGGCTCACAAAACTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_039299072.1\|4615345_4616023_-\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270620
NZ_CP009280.1\|WP_042137792.1\|4611376_4612309_-\|dihydroorotate-dehydrogenase	unknown	unknown	gnl\|CDD\|235982
NZ_CP009280.1\|WP_039299084.1\|4620138_4620861_-\|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224051
NZ_CP009280.1\|WP_042137801.1\|4616415_4618536_+\|polyphosphate-kinase-1	unknown	unknown	gnl\|CDD\|235469
NZ_CP009280.1\|WP_042137807.1\|4622902_4624648_+\|alpha-glycosidase	unknown	unknown	gnl\|CDD\|200477
NZ_CP009280.1\|WP_052421910.1\|4624809_4625094_+\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915
NZ_CP009280.1\|WP_081970036.1\|4618483_4620043_-\|Ppx/GppA-family-phosphatase	unknown	unknown	gnl\|CDD\|223326
NZ_CP009280.1\|WP_039299069.1\|4614326_4615187_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|213022
NZ_CP009280.1\|WP_042137810.1\|4625151_4626588_-\|glycogen-synthase-GlgA	unknown	unknown	gnl\|CDD\|234809
NZ_CP009280.1\|WP_042137799.1\|4613092_4614133_-\|NADH:flavin-oxidoreductase/NADH-oxidase	unknown	unknown	gnl\|CDD\|239242
NZ_CP009280.1\|WP_042137817.1\|4634570_4635296_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|226164
NZ_CP009280.1\|WP_042137804.1\|4620847_4621507_-\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP009280.1\|WP_039299112.1\|4632556_4633255_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP009280.1\|WP_042141254.1\|4635385_4636522_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341030
NZ_CP009280.1\|WP_042137806.1\|4621645_4622461_-\|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270338
NZ_CP009280.1\|WP_042137793.1\|4612301_4613006_-\|dihydroorotate-dehydrogenase-electron-transfer-subunit	unknown	unknown	gnl\|CDD\|99814
NZ_CP009280.1\|WP_042137811.1\|4626618_4628538_-\|1,4-alpha-glucan-branching-protein-GlgB	unknown	unknown	gnl\|CDD\|235445
NZ_CP009280.1\|WP_039299109.1\|4631153_4632560_-\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP009280.1\|WP_042137813.1\|4628755_4629979_+\|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl\|CDD\|179997
NZ_CP009280.1\|WP_156118652.1\|4630071_4631157_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|224584

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_039299072.1\|4615345_4616023_-\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|270620	cd14667, 3D_containing_proteins, Non-mltA associated 3D domain containing proteins, named for 3 conserved aspartate residues. This family contains the 3D domain, named for its 3 conserved aspartates, including similar uncharacterized proteins. These proteins contain the critical active site aspartate of mltA-like lytic transglycosylases where the 3D domain forms a larger domain with the N-terminal region. This domain is also found in conjunction with numerous other domains such as the Escherichia coli MltA, a membrane-bound lytic transglycosylase comprised of 2 domains separated by a large groove, where the peptidoglycan strand binds. Domain A is made up of an N-terminal and a C-terminal portion, corresponding to the 3D domain and Domain B is inserted within the linear sequence of domain A. MltA is distinct from other bacterial LTs, which are similar to each other. Escherichia coli peptidoglycan lytic transglycosylase (LT) initiates cell wall recycling in response to damage, during bacterial fission, and cleaves peptidoglycan (PG) to create functional spaces in its wall. PG chains (also known as murein), the major components of the bacterial cell wall, are comprised of alternating beta-1-4-linked N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), and lytic transglycosylases cleave this beta-1-4 bond.	3.76339e-26
NZ_CP009280.1\|WP_042137792.1\|4611376_4612309_-\|dihydroorotate-dehydrogenase	gnl\|CDD\|235982	PRK07259, PRK07259, dihydroorotate dehydrogenase.	4.19051e-150
NZ_CP009280.1\|WP_039299084.1\|4620138_4620861_-\|amino-acid-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	3.83869e-161
NZ_CP009280.1\|WP_042137801.1\|4616415_4618536_+\|polyphosphate-kinase-1	gnl\|CDD\|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP009280.1\|WP_042137807.1\|4622902_4624648_+\|alpha-glycosidase	gnl\|CDD\|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_CP009280.1\|WP_052421910.1\|4624809_4625094_+\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	0.00125881
NZ_CP009280.1\|WP_081970036.1\|4618483_4620043_-\|Ppx/GppA-family-phosphatase	gnl\|CDD\|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	1.59934e-93
NZ_CP009280.1\|WP_039299069.1\|4614326_4615187_+\|polysaccharide-deacetylase-family-protein	gnl\|CDD\|213022	cd10917, CE4_NodB_like_6s_7s, Catalytic NodB homology domain of rhizobial NodB-like proteins. This family belongs to the large and functionally diverse carbohydrate esterase 4 (CE4) superfamily, whose members show strong sequence similarity with some variability due to their distinct carbohydrate substrates. It includes many rhizobial NodB chitooligosaccharide N-deacetylase (EC 3.5.1.-)-like proteins, mainly from bacteria and eukaryotes, such as chitin deacetylases (EC 3.5.1.41), bacterial peptidoglycan N-acetylglucosamine deacetylases (EC 3.5.1.-), and acetylxylan esterases (EC 3.1.1.72), which catalyze the N- or O-deacetylation of substrates such as acetylated chitin, peptidoglycan, and acetylated xylan. All members of this family contain a catalytic NodB homology domain with the same overall topology and a deformed (beta/alpha)8 barrel fold with 6- or 7 strands. Their catalytic activity is dependent on the presence of a divalent cation, preferably cobalt or zinc, and they employ a conserved His-His-Asp zinc-binding triad closely associated with the conserved catalytic base (aspartic acid) and acid (histidine) to carry out acid/base catalysis. Several family members show diversity both in metal ion specificities and in the residues that coordinate the metal.	3.80442e-79
NZ_CP009280.1\|WP_042137810.1\|4625151_4626588_-\|glycogen-synthase-GlgA	gnl\|CDD\|234809	PRK00654, glgA, glycogen synthase GlgA.	0
NZ_CP009280.1\|WP_042137799.1\|4613092_4614133_-\|NADH:flavin-oxidoreductase/NADH-oxidase	gnl\|CDD\|239242	cd02932, OYE_YqiM_FMN, Old yellow enzyme (OYE) YqjM-like FMN binding domain. YqjM is involved in the oxidative stress response of Bacillus subtilis. Like the other OYE members, each monomer of YqjM contains FMN as a non-covalently bound cofactor and uses NADPH as a reducing agent. The YqjM enzyme exists as a homotetramer that is assembled as a dimer of catalytically dependent dimers, while other OYE members exist only as monomers or dimers. Moreover, the protein displays a shared active site architecture where an arginine finger at the COOH terminus of one monomer extends into the active site of the adjacent monomer and is directly involved in substrate recognition. Another remarkable difference in the binding of the ligand in YqjM is represented by the contribution of the NH2-terminal tyrosine instead of a COOH-terminal tyrosine in OYE and its homologs.	1.16722e-162
NZ_CP009280.1\|WP_042137817.1\|4634570_4635296_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|226164	COG3638, COG3638, ABC-type phosphate/phosphonate transport system, ATPase component [Inorganic ion transport and metabolism].	1.16103e-71
NZ_CP009280.1\|WP_042137804.1\|4620847_4621507_-\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	3.04469e-83
NZ_CP009280.1\|WP_039299112.1\|4632556_4633255_-\|response-regulator-transcription-factor	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	6.32746e-82
NZ_CP009280.1\|WP_042141254.1\|4635385_4636522_-\|MFS-transporter	gnl\|CDD\|341030	cd17477, MFS_YcaD_like, YcaD and similar transporters of the Major Facilitator Superfamily. This family is composed of Escherichia coli MFS-type transporter YcaD, Bacillus subtilis MFS-type transporter YfkF, and similar proteins. They are uncharacterized transporters belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	6.90125e-69
NZ_CP009280.1\|WP_042137806.1\|4621645_4622461_-\|transporter-substrate-binding-domain-containing-protein	gnl\|CDD\|270338	cd13620, PBP2_GltS, Substrate binding domain of glutamate or arginine ABC transporter, a member of the type 2 periplasmic binding fold protein superfamily. This family comprises of the periplasmic-binding protein component (GltS) of an ABC transporter specific for glutamate or arginine from Lactococcus lactis, as well as its closely related proteins. The GltS domain belongs to the type 2 periplasmic binding protein fold superfamily (PBP2), whose many members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	7.96713e-89
NZ_CP009280.1\|WP_042137793.1\|4612301_4613006_-\|dihydroorotate-dehydrogenase-electron-transfer-subunit	gnl\|CDD\|99814	cd06218, DHOD_e_trans, FAD/NAD binding domain in the electron transfer subunit of dihydroorotate dehydrogenase. Dihydroorotate dehydrogenases (DHODs) catalyze the only redox reaction in pyrimidine de novo biosynthesis. They catalyze the oxidation of (S)-dihydroorotate to orotate coupled with the reduction of NAD+. In L. lactis, DHOD B (encoded by pyrDa) is co-expressed with pyrK and both gene products are required for full activity, as well as 3 cofactors: FMN, FAD, and an [2Fe-2S] cluster.	7.42783e-79
NZ_CP009280.1\|WP_042137811.1\|4626618_4628538_-\|1,4-alpha-glucan-branching-protein-GlgB	gnl\|CDD\|235445	PRK05402, PRK05402, 1,4-alpha-glucan branching protein GlgB.	0
NZ_CP009280.1\|WP_039299109.1\|4631153_4632560_-\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.23242e-61
NZ_CP009280.1\|WP_042137813.1\|4628755_4629979_+\|glucose-1-phosphate-adenylyltransferase	gnl\|CDD\|179997	PRK05293, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_CP009280.1\|WP_156118652.1\|4630071_4631157_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	2.78991e-27

>NZ_CP009280.1|WP_042137806.1|4621645_4622461_-|transporter-substrate-binding-domain-containing-protein
MNKWGKLSLGLLLAAGLLAGCGSNNNENNTAASGNANTGAAAKKLIMGTSADFPPYEFHKVVDGQDTIVGFDIEIAKEIAADLGRELEIKDLPFDSLLNELSSGRIDMVISGLSPTPERAEAVGLSDIYYKAEQAVVVRESDKDKYATMDSLKGAKLGIQTGSIQEDIAKDIEGAQLTSLSKISEIVLQLQSNRVDASIMEGPVAKSFVKNVKGLVITDAKPEVEDDGYVIGVKKGNTELLDQVNKTLTRLNSEGKIDEYVAAASELAESK
>NZ_CP009280.1|WP_042137804.1|4620847_4621507_-|amino-acid-ABC-transporter-permease
MNIFDMAYEYRNFFLSGLKYTLLLAVLGVFFGFILGILVSLLRMSKWRILRFIATTWVEFLRGTPMLVQLFLIHYGLTELGLEFTPIQSGAITLTINSSAYLAEIFRAGIQGVDRGQVEAARSLGMKQGMTMRYIVLPQAIKNVLPAIGNEFITIIKESSIVSMIGVADLFFQAKTITTITYEGLTPYVVIALMYFVLTFTLSKLLGILERRLNTDDRG
>NZ_CP009280.1|WP_039299084.1|4620138_4620861_-|amino-acid-ABC-transporter-ATP-binding-protein
MIEVKNLQKSFGKLEILKGIDLNIHKGEVVVVIGPSGSGKSTFLRCLNLLEQPTGGEISFEGQSITAKKHDINVTREKMGMVFQQFNLFPHKSVLQNIMLAPLKVRKQQASEAEKIATELLRTVGLEDKRDAYPAQLSGGQKQRIAIARALAMQPHVMLFDEPTSALDPEMVGEVLEVMKQLAVDGMTMVIVTHEMGFAREVGDRILFMDGGVIVEQGTPAEVFGNPKHARTRDFLSKVL
>NZ_CP009280.1|WP_081970036.1|4618483_4620043_-|Ppx/GppA-family-phosphatase
MINLLEREYIQMRDDLCRIGIIDIGSNSIRLVIYDTTQAGGYKIIKECKYSARLSEKITKEGRLEKKDMDTIIPVLHQFKEICDDFEVDNIRAGATAAIRNAANSAEIISYLSEASSIRIEVISGHQEAYFGFLGVINAFDIQDGFVIDIGGGSTEVTLFRGRRYQHSISFPFGAVNTNLMFSQGGNWNADQVRKLQLYVTGRLVEHDWLTTGNGLPLYGLGGTLRSLGKLDQKNREYSLPNSHGYVLEGETIEKFMETLPATPYEKRKDLDGLSKSRGDIIVSGLVIFHTVYHYIGASRAVISGEGLREGMLHDLLKPEQPVRDSALEYSLDTIIRFDIRTSKRHLDHIYKLALGLLGAFEREGDREEHEMLIYVAIMLHRTGSNINYYQSKRHTRYWLMNSPIRGLTHRQLILSAYIASYSTKSRKQKLSQMHKDILLASDEEWIHKLGTLVQLSIALDSTEIGIVSGVNARLHNNTLDLELQGGQVLIGLEDIENALKAFRNAWSVKVKLGFPSSG
>NZ_CP009280.1|WP_042137801.1|4616415_4618536_+|polyphosphate-kinase-1
MNVNAEEKKNNHTSPATAYLNRDLSWIEFNRRVLAEAQDPENPLMERAKFLAIVSSNLDEFISVRVAGIQDQIRAGYTKKDFTGYTPSGLYKRLIKRVTKIIADQYRTFKDISRSLHKEGIVFVDYKDLTHAQEQSIEQYYRDIIYPVLTPMAVDQSRPFPLVHSQFIYLAVVLTRKNSQEEEPYFAILQIPSNLPRCIPLPHRSNSKKRQFVFIEDVIRQHIQTLFSGYDPVAVSEFRLTRNSDLTIDEEGAEDLLEEIEKELRKRRRGVPARLEVQKGIHPYALEQLQAEFELEDFVFEIEGPLDLSFLRGFAGSVKGFSYLHHAPIEPLYPAEFEENEDFFEVLGERDVLVYHPYESFDAMTDFIIQASEDEQVMAIKMTLYRVSGNSPLITALANAAESGKQVTVVVELKARFDEERNIAWARKLEQSGCHVVYGLVGLKTHAKVTLIVRQEGPELRRYVHVGTGNYNDSTAKAYTDLSLFTANHEIGLDASELFNQMTGYSANYNWNSFIVAPTNMSLSLQKLILREAEHAAAGRPARIIAKMNSLSNQEVIDNLYSAAQAGVSIDLIVRGVCCLRPGIEGLSERITVRSIVDRFLEHSRIYYFENGGKPEVYLSSADWMTRNLTRRIELMCPVKDSSIRKQIVKILDLSLMDNVKSSFLQPNGYYERADDKKAPFRSQFAAMNVTRWKGSRALPSPTKHS
>NZ_CP009280.1|WP_039299072.1|4615345_4616023_-|LysM-peptidoglycan-binding-domain-containing-protein
MKIKFGAITALAAVLGLGTLLQAAPVQADSVHIAGEATTFYTLSNHYDISVEELMSANPQISASNIYPGLKLAIPGTVQAKTVAVTESAAAAVVTNADLSALSVEPASNTVQAWGKAYTYAKSIQVKASAYSSAASENGKWGAVDYFGNALKLGTIAVDPSVIPLGTKVLVTGYSHPGLPKQAFLATATDMGSAIKGNRIDIFIPGSQSFVADFGYQYVQLYIIQ
>NZ_CP009280.1|WP_039299069.1|4614326_4615187_+|polysaccharide-deacetylase-family-protein
MKLARIRRILLLIFIIIVILPSIFPIAVSASASAPASARPNVSMEEDPAVPAGSTASQSSARRHKRNKGLSLSQLLRKYPDTIKTQGPRRKIIALTFDDVPDPRFTPQLLDVLHKYNVKATFFVVGSRAEKHPGLVARIIREGHAIGNHSYNHPEFGKLGMNEFRTQIIRTENIIQALAGYKPRLIRPPYGDISEQQLKWARAHGYKLVNWNVDSLDWRGLSKTQVRNNILSRAGKGAIILQHGGGGRGSNLQGTIQALPEVISIMRKRGYSFVTVPQMFEVSKSK
>NZ_CP009280.1|WP_042137799.1|4613092_4614133_-|NADH:flavin-oxidoreductase/NADH-oxidase
MTDLFAPYELKALTLKNRVVMPPMCQYAVEKQDGIPTDWHFVHYVSRAVGGTGFIIVEMSGIHPDGRITNQDTGIWEDGQIAAFKRITEAVHAQGAKIAIQLGHAGRKAVDANPPVAPSAIPFDAHSQTPRALTRDGIAEMIGAYRDAARRAVEAGFDTVELHGAHGYLIHQFHSPLSNVRDDEYGSDPALFGEQVVEAVREVLPAEMPLLMRVSAKEYVEGGYNEAYALEFCRRYKAAGVDMFHVSSGGEGPIGSNGGPNAGPAYQVELAEYIRSGLQVPVIAVGRLESYGEAQAVITEARAELVAVGRGMLSDPYWTLHAEEALGGVHQANLPKPYLRGIWNKK
>NZ_CP009280.1|WP_042137793.1|4612301_4613006_-|dihydroorotate-dehydrogenase-electron-transfer-subunit
MATVISNERLGDGVYHLVVEGGNGGAMGQFYMLRAWGAYPLLSRPLSIHQVNDSGVDFLYHVVGEGTEILAGLKPGDKLELEGPFGTGFPHVEGKVALVGGGIGIAPLYYCAQELPESDIYLGFSREPFRTEAFRPLAAELTVDVGGHILDSVDFTAYDHIFVCGPHPMLKAAQLKGIAAETAGKRPDVYLSLENRMACGIGACLVCSVSCKDGQRKACADGPVFLAGEVLFHD
>NZ_CP009280.1|WP_042137792.1|4611376_4612309_-|dihydroorotate-dehydrogenase
MINTTATIAGVHFKNPIVMASGTFGFGREYGKLYDVSLLGGISGKGLTLHAKAGNPGVRVYETASGMLNSVGLENPGVEAFLAKELPYWETLDTARIVNLGGNTLADYVLGAELIQRDADARLLTGKPAVDMIELNISCPNVKEGGIAFGVKTPAALEVVRAVRAATRLPLAVKLSPNAEDIAEMAEMCEAEGADAVSLINTISGMKIDVRRRRSVFNNLYAGLSGPAIKPVALRMVHQVSKRVSIPVIGMGGITSATDIIEFIMAGAAVIQVGTYNFMNLRAGSTLVEELQQFMAEENISSLDEIRGIV
>NZ_CP009280.1|WP_042137807.1|4622902_4624648_+|alpha-glycosidase
MLLEAMYHVPRDKWAYAYDATTIHLRVRTKRDDVDYVVALTGDKYDWQHTSYDIIMEKAASDDKFDYWEAAVRPKYKRLSYTFRVSKGSETVYLLDNGIRTECPQPPNHFYEFPYIHGIDLFKVPTWAKDAVFYQIMTERFANGNPLNDPEGTEPWGGKPKLDNFFGGDLQGVLDHLDDLQELGINAVYFTPLFVSPSNHKYDIVDYKKVDPNFGDNELLKKVVEECHKRGIRVMLDAVFNHCSDKFPPFQDVLEKGEFSVYRDWFHMNSFPAEIVDGIPTYDTFGFYGNMPKFNTANHEVKSYLLEVAEYWIKEIRVDGWRLDVANEVDHHFWRDFRKVVKAANPDAYIVGEVWSDSLTWLLGDQFDSVMNYPFSGAVLEFFNGGMDGITFGHRIGSLLMRYPQQTNEVVFNLLGSHDTPRLLTVLGEDKRKLKLTVVFLFTFMGTPCIYYGDEIGLTGGEDPDCRKCMEWDETKQDRELYDFYRMMIALRKEHKALREGRFRILQACENDPCIVYERADERIHFTVWMNNSPQPRTLSHPMETDDWLDALTGEAVVPENGMMNVALDPYGYRILYRNLS
>NZ_CP009280.1|WP_052421910.1|4624809_4625094_+|nuclear-transport-factor-2-family-protein
MIEREQVIEKYFQSWIHKNNSILSQIFDPNIAYTECYGPEYHGLATITKWFDDWNTRGTVLVWTIKQFIHQGSMTAVEWYFKCEYESVLSLYII
>NZ_CP009280.1|WP_042137810.1|4625151_4626588_-|glycogen-synthase-GlgA
MKVLFAAAEAHPFIKTGGLADVIGALPKALKAAGVDVRVILPKYKGIAEKYSSQMEHVAVLEVPIGWRNQYCGIERIVFEGVPVYFIDNEYYFGRDGIYGYMDDGERFAFYNRAVLECLPAINFQPDVLHCHDWHAAVIPLLLQAHYRHNPFYSEMRTVFTIHNLLYQGVFPYSVLGELLGLDDSYFPGVEYYGNVNYMKGGIVYSDHVTTVSPTYADEIRTPYYGYGLDGLLTSRSDALSGIVNGIDTKSYNPASDPSIFTRYRSNLVKKAENKLGLQQELGLPVAPYIPMVAMVTRLVDSKGLDLLTRVLDELLYYDDIQFVLLGTGDEVYERWFREAQWRYPTKLSSQILFNDALSRKIYAASDLFLMPSKFEPCGISQLLALRYGSIPVVRETGGLNDTVQAYNEETGEGNGFTFKDYNAHDMMYTLRRAVSFYHKPEHWKKVAKNAFTGDYSWNVSAQQYIDIYNKISDKVTE
>NZ_CP009280.1|WP_042137811.1|4626618_4628538_-|1,4-alpha-glucan-branching-protein-GlgB
MAEIPKTVNLPSSEDIYLFHEGTNYRSYTMLGAHIAVEEGQAGVRFTVWAPHAAYVGLAGDHNGWDGTLDSDSLYKIPDSGFWSRFFPGIEPGTFYKYRIHGADGTSFLKADPYAFKAEVRPATASVVANLDGYQWGDAAWRRKSKAPYNAPMNIYEMHFGTWRQKDNGELYTYREMSSLLIPYLTEMSYTHVEFMPLAEHPYDLSWGYQGTGYFAATSRFGDPQDLMYLIDQLHQAGIGVILDWVPAHFAKDAHGLRMFDGSPLYEYADPMLAEKPGWGTLSFDFSKPEIISFLISNALFWFEMYHIDGMRVDAVTSMLRLDFEKQHHQYTKNMHGGLENLEAIAFIQQLNTAIFRYYPKALMMAEESSAWPGVTSPVHEGGLGFNYKWNMGWMNDTLGYIEHDFGARPYHHNLLTFPIVYAYAENYTLPLSHDEVVHGKKSLLNKMPGSYEQKFAGLRALLGYQISHPGKKLLFMGGEFGQFIEWKDQDQLDWLLLEYEAHRRMLAYTAALNKLYLTQKALWELDHDMEGYQWIDADDSGQSVASYIRRGKRPVDTLVIIINFQPVERRNYRIGVPRPGTYEEIFSSETREYGGSGIHNEPVKSEKKEWHNQLNSLELTLPPLGFLVLKKSGRKTIK
>NZ_CP009280.1|WP_042137813.1|4628755_4629979_+|glucose-1-phosphate-adenylyltransferase
MSKKDCIAMLLAGGEGRRLAPLTSSMAKPAVPFGGQYRIIDFPLSNCVNSKIDTIGVLTQYEADSLHHHIGEGEPWGLHSRSDKGVKLLPSGVEGRDTYSGTADAIYKNIEYIDSQNPEHVLILSADHIYHMDYRKMLDYHVGKAAKATISVMEVPWDEASRFGVMNVNDDLQISEFAEKPKVPKSNLASMGIYMFEWEYLKGYLLRDAANSESGHDFGKDVIPSMLDANDQLFAYRFDGYWRDVGTVDSLWEAHMDLLQSENGFKLDNSRWPMYSRSYRTKLAAYKPRVQAPPADCLMHETCTLEGNLQRSVIFGGVEIGKLSKIKQSVIMPGVRIGRGVLIENAIIGEGAVIKDGAVIKGSADNIVVVGPHEIVAAKPIIRTQPSRLLQEVYEKTGRLRAEGMPS
>NZ_CP009280.1|WP_156118652.1|4630071_4631157_-|GNAT-family-N-acetyltransferase
MNTQESGKSSSEQRLEMIRGGREHSADILKLLREAAGWMESKGINQWTPGQFSIRDVEDYLSSREVYLAMEGAALAGMFTLQFSDIQYWGDRNDESYAYLHRLAVAKSHRGMGLGGQMIRFALRRAEERGCAGLRLDTVAHNIKLNRYYQSLGFHYMGTRDVGAGRLVNLYEYEAETGDPGSVILRYMGEADYALMREWSVSPEYLKKWAGPSLSYPLDDRQLERYLDGANHPAESGLLVYCAVLRATGQTVGHISLSGIDRENGSARISRVVVDPGSQGRGIGLQMVREVLRIGFEGLRLHRISLGVFDFNTAAQKTYETAGFTREGISREAATFGGRYADCIEMGILDREWRANRPSGK
>NZ_CP009280.1|WP_039299109.1|4631153_4632560_-|HAMP-domain-containing-histidine-kinase
MIKKGMRRQIVLHYILVVFVALLLVETIFLLAIRTYYYDSIYSKITTHISAGETFVKYEFSAERSPNQLLNLLDFFNLEYTELEVLTLNGDIITSSTGFQPDRTITTSDVPEAVGGSVGRWVGRQAGTNESVMAVSKMVQINSHETYILRYLTSMEGVNKDLLNLTLLSIGIGAAVMSIVVLFSFGLANSIVRPLNNITAVSAQMAKGKFTTRIKGDYRYEIAELASTLNYMAEEIVRSNQIKDDFISSISHELRTPLTSIKGWSETLISGGYDPEETKLGMGIISKESDRLIGLVEEILDFSKLQQNEMKLSITQVDIKVLLQETLLNIWAKAEKKRIHLLLECEETIYIRGDANRLKQVFLNLVDNAVKFSPEDSSIVLSAERLSNTEMAVIVRDSGIGISEAHLSRVRDRFFQVDALNGGTGLGLAISQQIVELHNGKLEMDSELGKGTQVTVILPLDDVQEEKA
>NZ_CP009280.1|WP_039299112.1|4632556_4633255_-|response-regulator-transcription-factor
MSKVLILEDEESIRSFIVINLKRNGFEVLEAADGNEALHKLTTVPDIDIALLDVMVPGIDGFEVCRRIRETNERLGIIFLTAKVQEQDKVYALSVGADDHVSKPFSPTELIARIQSLLRRVNVHREQSAKVSFHSGPFTLDLISKQFKKSGEAIELTPTEFSLVQFFLEKENTPLSRDSLLDHVWGKEYMGDPKIVDVNIRRLRQKIENNPSEPEFLQTVWGHGYKWKGQVQ
>NZ_CP009280.1|WP_042137817.1|4634570_4635296_-|ATP-binding-cassette-domain-containing-protein
MITVEHLAKAVGEDKAPVLQDIGFQLEPGEFVVILGASGSGKSTLLKCLALREKWDRGNFRVDGKDIMKSPFAGKRKIRREWAYLEQNAELNPNRTALKNVLIGQASQTPLWRMATGMVRSDDYMGAMDQLDLLGLLDKAKMKTSHLSGGERQRVAIARALVHGAKVILADEPVTGLDPKTAENVLETLRKLCKETGLTVITVLPIELAERFASRLWVLEDGRIKHDVKGRRLTSQERLHL
>NZ_CP009280.1|WP_042141254.1|4635385_4636522_-|MFS-transporter
MNYMILITVIILAGLSQGMLLPVLSILLEQKGVSSSLNGLNAAALYVGSFAMTLIAERVLGAIGFKKLIAAGLSLVLVTLLLFPLLPGVKVWFVLRLLVGIGDSAINYAAQLWVLLMSPAEHRGRNLSLYGMSYGLGFSLGPLGIILLRFGPSAPFLITAGLFVLVLLLVAVKLPDSRPHPIDHSEGQARRFGRSYRLAWYALIPALLYGYMEASLNSNFPVYGLRIGFSTDQIATLLPFAGIGGLLLQLPLGIWSDRYGRRAILIASGVGGGLAFTLLPLAGEHFLLNLLLLMIAGGLVGSFFSLGLSYAADILPRHLLPAANVVSSFHYSLGSIAGPGVGGLLLQFGWGGSVFAVMGGLYILFGLTGLLFSPRKII

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_CP009280_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_13

4834455-4834557

Orphan

Consensus_repeat	Method
ACTGCCCGACGCGCTTTTCGCTCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_13

>merge|NZ_CP009280|13|4834455-4834557|CRISPRCasFinder
ACTGCCCGACGCGCTTTTCGCTCCGTTGCCCGCATAGCCACTACCCGACGCGCTTTTCGCTCCGCTGCCCGCATAGCCACTGCCCGATGCGCTTTTCGCTCCG

>NZ_CP009280|13|11|4834455-4834557|CRISPRCasFinder
ACTGCCCGACGCGCTTTTCGCTCCG	TTGCCCGCATAGCCACTACCCGACGCGCTTTTCGCTCCGCTGCCCGCATAGCC
ACTGCCCGATGCGCTTTTCGCTCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042138064.1\|4828443_4830327_-\|molecular-chaperone-HtpG	unknown	unknown	gnl\|CDD\|235366
NZ_CP009280.1\|WP_042138056.1\|4822921_4824661_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP009280.1\|WP_042138075.1\|4845321_4846386_-\|recombinase-RecA	unknown	unknown	gnl\|CDD\|236476
NZ_CP009280.1\|WP_042138070.1\|4831752_4832649_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP009280.1\|WP_042138071.1\|4832768_4833644_+\|4-hydroxy-tetrahydrodipicolinate-synthase	unknown	unknown	gnl\|CDD\|188637
NZ_CP009280.1\|WP_042138058.1\|4824657_4826397_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP009280.1\|WP_042138074.1\|4844452_4845187_-\|RecX-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|237619
NZ_CP009280.1\|WP_042138062.1\|4827854_4828361_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_144026167.1\|4839872_4840847_-\|membrane-dipeptidase	unknown	unknown	gnl\|CDD\|366534
NZ_CP009280.1\|WP_042138066.1\|4830551_4831004_+\|DNA-gyrase-inhibitor	unknown	unknown	gnl\|CDD\|225980
NZ_CP009280.1\|WP_039294751.1\|4839145_4839718_-\|phosphate-propanoyltransferase	unknown	unknown	gnl\|CDD\|237899
NZ_CP009280.1\|WP_042138077.1\|4846671_4847961_-\|competence/damage-inducible-protein-A	unknown	unknown	gnl\|CDD\|234789
NZ_CP009280.1\|WP_042138055.1\|4821823_4822399_-\|histidine-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|366010
NZ_CP009280.1\|WP_052421918.1\|4836001_4838950_-\|EAL-domain-containing-protein	unknown	unknown	gnl\|CDD\|236645
NZ_CP009280.1\|WP_042138060.1\|4826567_4827437_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP009280.1\|WP_039294761.1\|4841546_4842341_-\|TIGR00282-family-metallophosphoesterase	unknown	unknown	gnl\|CDD\|379099
NZ_CP009280.1\|WP_039294762.1\|4842602_4844144_-\|ribonuclease-Y	unknown	unknown	gnl\|CDD\|237177
NZ_CP009280.1\|WP_042138068.1\|4831005_4831692_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293807
NZ_CP009280.1\|WP_039294770.1\|4848020_4848608_-\|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase	unknown	unknown	gnl\|CDD\|273139
NZ_CP009280.1\|WP_019910496.1\|4841083_4841344_-\|stage-V-sporulation-protein-S	unknown	unknown	gnl\|CDD\|225234

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042138064.1\|4828443_4830327_-\|molecular-chaperone-HtpG	gnl\|CDD\|235366	PRK05218, PRK05218, heat shock protein 90; Provisional.	0
NZ_CP009280.1\|WP_042138056.1\|4822921_4824661_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP009280.1\|WP_042138070.1\|4831752_4832649_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	2.1738e-58
NZ_CP009280.1\|WP_042138071.1\|4832768_4833644_+\|4-hydroxy-tetrahydrodipicolinate-synthase	gnl\|CDD\|188637	cd00950, DHDPS, Dihydrodipicolinate synthase (DHDPS). Dihydrodipicolinate synthase (DHDPS) is a key enzyme in lysine biosynthesis. It catalyzes the aldol condensation of L-aspartate-beta- semialdehyde and pyruvate to dihydropicolinic acid via a Schiff base formation between pyruvate and a lysine residue. The functional enzyme is a homotetramer consisting of a dimer of dimers. DHDPS is member of dihydrodipicolinate synthase family that comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways.	5.45284e-102
NZ_CP009280.1\|WP_042138058.1\|4824657_4826397_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.42568e-160
NZ_CP009280.1\|WP_042138075.1\|4845321_4846386_-\|recombinase-RecA	gnl\|CDD\|236476	PRK09354, recA, recombinase A; Provisional.	0
NZ_CP009280.1\|WP_039294751.1\|4839145_4839718_-\|phosphate-propanoyltransferase	gnl\|CDD\|237899	PRK15070, PRK15070, phosphate propanoyltransferase.	6.39357e-119
NZ_CP009280.1\|WP_144026167.1\|4839872_4840847_-\|membrane-dipeptidase	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	8.46948e-81
NZ_CP009280.1\|WP_042138066.1\|4830551_4831004_+\|DNA-gyrase-inhibitor	gnl\|CDD\|225980	COG3449, COG3449, DNA gyrase inhibitor [DNA replication, recombination, and repair].	1.53001e-39
NZ_CP009280.1\|WP_042138074.1\|4844452_4845187_-\|RecX-family-transcriptional-regulator	gnl\|CDD\|237619	PRK14135, recX, recombination regulator RecX; Provisional.	1.5185e-34
NZ_CP009280.1\|WP_042138077.1\|4846671_4847961_-\|competence/damage-inducible-protein-A	gnl\|CDD\|234789	PRK00549, PRK00549, competence damage-inducible protein A; Provisional.	0
NZ_CP009280.1\|WP_042138055.1\|4821823_4822399_-\|histidine-phosphatase-family-protein	gnl\|CDD\|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.53214e-51
NZ_CP009280.1\|WP_052421918.1\|4836001_4838950_-\|EAL-domain-containing-protein	gnl\|CDD\|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	3.89296e-116
NZ_CP009280.1\|WP_042138060.1\|4826567_4827437_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	3.39249e-49
NZ_CP009280.1\|WP_039294761.1\|4841546_4842341_-\|TIGR00282-family-metallophosphoesterase	gnl\|CDD\|379099	pfam13277, YmdB, YmdB-like protein. This family of putative phosphoesterases contains the B. subtilis protein YmdB.	5.29938e-155
NZ_CP009280.1\|WP_039294762.1\|4842602_4844144_-\|ribonuclease-Y	gnl\|CDD\|237177	PRK12704, PRK12704, phosphodiesterase; Provisional.	0
NZ_CP009280.1\|WP_042138068.1\|4831005_4831692_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293807	cd07721, yflN-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis yflN; MBL-fold metallo hydrolase domain. This subgroup includes the uncharacterized Bacillus subtilis yflN protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	2.75718e-57
NZ_CP009280.1\|WP_039294770.1\|4848020_4848608_-\|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase	gnl\|CDD\|273139	TIGR00560, pgsA, CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase. Alternate names: phosphatidylglycerophosphate synthase; glycerophosphate phosphatidyltransferase; PGP synthase. A number of related enzymes are quite similar in both sequence and catalytic activity, including Saccharamyces cerevisiae YDL142c, now known to be a cardiolipin synthase. There may be problems with incorrect transitive annotation of near homologs as authentic CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase. [Fatty acid and phospholipid metabolism, Biosynthesis].	3.84608e-54
NZ_CP009280.1\|WP_019910496.1\|4841083_4841344_-\|stage-V-sporulation-protein-S	gnl\|CDD\|225234	COG2359, SpoVS, Stage V sporulation protein SpoVS [Function unknown].	1.33023e-44

>NZ_CP009280.1|WP_042138071.1|4832768_4833644_+|4-hydroxy-tetrahydrodipicolinate-synthase
MLTEEQIYGIYVPVVTPFHAAGEIDLESYQRYVNNIIKNSIHGLVVNGTTGESPTVNIQELQTLVDASRELLKNTSIPLVVGTGTNDTMSTVTRTELAANSGADAALVVVPYYSRPSQEGIIAHFRKAAEVGLPIIAYDIPGRAGVGMSVDTARTILEMNNVVGLKDCSGSPVLVSELSRHGSKPVLCGDDLNFFDMLGCGAAGGMLASANVHTASYLSIYEQYRAGQVEAARAAFDQLVPLMKLLFKESNPAPIKWLLSARGEISSDTLRLPMTSISAALREELGAYLAG
>NZ_CP009280.1|WP_042138070.1|4831752_4832649_-|LysR-family-transcriptional-regulator
MDLTYMRTFREVAKRQSFTRAAEELGYAQSSVTMQIQKIEKEYGVPLIERHGRALRLTPPGEELLKLFVEILDLYDRSKETIAQQIGGTLTIGTIDSLAAFYLPPFLQQLRTMFPGLNIHLQTEQEANLVSKIRDGEVDIGLLLDRSTADILLERTIIREEPLVLVAPASHPLASVAQVTLQDLNNCELIVSEESCIYRSLFENLLREHGIVFRIGFELSNLEAIKRCVRNGLGIALLPRIVAEEEIERGNLAELSFAHPEIHFDLQLLLHPKKWKSLPLQSLIQMLREDAKAKAAIL
>NZ_CP009280.1|WP_042138068.1|4831005_4831692_-|MBL-fold-metallo-hydrolase
MDIIELPIQFEYEGQPYYIYPSLIVSGEELTLVDTGYPTFMPLIEKKILELGYDPLNLKNIIITHYDDDHIGALYEFVEKYPSVTVMASEVDTPSISGLVKSERLVQAEALLVEMPKEEQASGEEFVQLLKNLRHVPVKQTVREGQCILDGKCQVLATPGHTSGHISLYFPELSSVITGDAAVSEENELAVANPQYCFDLESAEQSLNRLQALNARSYYCYHGGKLGF
>NZ_CP009280.1|WP_042138066.1|4830551_4831004_+|DNA-gyrase-inhibitor
MKIQLQTLPVTRIAYVRQTGPYGPGNSKAMGALKEWARAHRLLTGSAILFGIPQDNPDTTLPEHCRYDACISVLENAPADKSINYGEIPGGTYAVVTIQHTAEAVQKAWTEILPALYVSGHQLDYQRPVMERYTGDMISNHLCQLCFPVH
>NZ_CP009280.1|WP_042138064.1|4828443_4830327_-|molecular-chaperone-HtpG
MAKKEFKAESKRLLEMMINSIYTQREIFLRELISNASDAIDKIYYKALADEGLVFNKEDYYIKVTADKASRTLTISDTGIGMTQEELENNLGIIANSGSFAFKKDNEAKDGHNIIGQFGVGFYSAFMVADDVTVISKALGSDQAFKWESQGADGYTIEPCEKDAVGTEITLKIKENTEDDNYDEFLEEYRLKSIIKKYSDFIRFPIKMDITGRQPKEDAENEFVDVIEEQTVNSMVPIWRKNKNELTEEDYNNFYAEKRYGFDKPLKHIHISADGAVVYNAILFIPENTPFDYYTKEYEKGLELYSNGVLIMNKCGDLLPDYFSFVKGMVDSEDLSLNISRELLQHDRQLTLIAKNIKSKIKSQLLSLLKDEREKYETFYKSFGRQLKFGVYNDYGMEKETLQDLLMFHSSKEKKLVTLAEYVERMPEDQKFIYYASGESVERIEKLPQTEMVLDKGYEILYFTDDIDEFAIKMIMSYKEKEFKNVSSGDLGIEESAEDKPSEAEENENKGLFEAMQGILSGKVKAVKASKRLKSHPVCLSTEGELTIEMEKILKAMPNGGQDVQADKVLEINIHHDVFKSLKAAAEGDKEKLGLYTNLLYNQALLIEGLQVNDPVQFTNDICKIMV
>NZ_CP009280.1|WP_042138062.1|4827854_4828361_+|hypothetical-protein
MLPTKRSLVTAVISTVIFYSSGIAAGDISDLSSKEEGVITAHDTERLKSLGIQLHLPTSSNLVITKEQAISLAHTSAPKFASEAPEVIIEYQLLTYPYLTAFSEQALNKNANLRADGYLNNTPVYIVTFKGIHGTGHAARGQKVPTYKEFNVVIDASSGETLFSFTYK
>NZ_CP009280.1|WP_042138060.1|4826567_4827437_+|LysR-family-transcriptional-regulator
MDIRQLKYFLAIAEEGQITSAARKLQMAQPPLSQQLKLLEEELGVKLVERGPRSIQLTDAGIILRNRAQQILELTDSTTREINDFAKGLKGSLSIGTVSSSGATLLHDRLGEFHKNYLGVTFEIHEGNTFMIIDLLNKGIVEIGIIRTPFNSSNLECLYLNSEPMIAVMTPDYDWNSSEAAISLGELQHKPLIIYRRFEQLIRETCLEHGFEPQIFCMNDDARTTLLWANAGLGIGIIPKSAFELANHSNLIFKEIRCEALHTRVAAVWIKDKYLSSLATKFIETFRAR
>NZ_CP009280.1|WP_042138058.1|4824657_4826397_-|ABC-transporter-ATP-binding-protein
MFKIAVFLKPYRKEVIIGPIFKLLEAILELLLPTIVALIINNGIGRQDSAYVYRMGSLMVLMAILGFGCSMICQYYAARASQGFGTSLRNKMFKHISSLSYAELDIIGTPSLINRITNDVNQLQLAVAMLIRLVIRAPFICIGAIIMSMILDFRLSLILIAATPVFGVILYFIITRSSPLYRKYQAKLDRLALVLSENLSGIRVIRAFAESRREKQRFNEASEDLTQTAIRVGRISAWLGPMTTLVVNAAIIAILWAGGIHIDAGRLSQGEIIAFINYVTQILLALIVVSNLVILFTKASSSANRVNEVLAMTASVAEVAADAPPAKRDDSAPVISFRNVSFGYNTTGELALQNITVDIHRGETVGLIGSTGSGKSTFVNLIPRFYDAVEGEILVEGVNVRQYRLEQLRSRIGIVPQKAMLFTGSIADNIRWGKASATREEIMSAAAVAQAEEFIAKLPEGLDTLVARGGHNLSGGQKQRLTIARAVVGRPPVLILDDSSSALDFATDAALRRALNKNSGDMTVLLVSQRVSTVRQADQIIVFDEGRIAGIGSHEELLESCGVYQEICMSQLSSEEAVQ
>NZ_CP009280.1|WP_042138056.1|4822921_4824661_-|ABC-transporter-ATP-binding-protein
MNSTKTWKRLFRYTSQYRKITIGAVICAILSVIASLIGPLLIGRAVDHMIGPDQVDFPEIFRLLLILGAVYLVGSFFGWLLTYYTNKLAYRTVYDLRRELFDKLDALPLKFHDNHPQGDSISRFVNDMDAVSDGLLQGFSTLLTGIVTIAGAIGLMLYISPVMTLVVLLSAPATFFVARFITIRSQQMFREQAKILGGLNGYVEELVGGQKVVQAYHYEDRSFAGFAERNNELYKTGIKSQFYGSLSNPTTRLVNNITFSVIAMIGSALVIGGHFSVGDLSSFLIYSNLFAKPFNEITGVITQLQSATASAQRIFNILDLPQETQDAPGAVVMKGSQGTITFDKVSFAYTPERPLIRNFSLEVKPGTRVAIVGQTGAGKTTLVNLLMRFYEVDSGTIRIDGTDITSITRDSLRRNFGMVLQDTWLYGGSIRDNIAYGKPEASEAEVIAAAKAANAHSFIKRLPEGYNTKISGSGDNLSQGQKQLLTIARVMLVDPPMLILDEATSSIDTLTEVRIQKAFLAMISGRTSFVIAHRLSTIRESDLILFMKDGDIVESGTHEELVGSGGYYARLYNSQFMAV
>NZ_CP009280.1|WP_042138055.1|4821823_4822399_-|histidine-phosphatase-family-protein
MATIGLIRHGITEWNIAGRAQGLADIPLNREGREQAVKLAGRLRKERWDIMISSHLCRARETAEIIAAAAGIGEHLIDERICEMDCGQLEGLNEAEWLGRWGQDWRSLELGMETAEDVSRRGALVLEELYNRYGNKKILVVSHGALIGLTLQHLLPQVFTTTYIDNASLTLLTKTNNNWDCQLYNCVEHLV
>NZ_CP009280.1|WP_052421918.1|4836001_4838950_-|EAL-domain-containing-protein
MNQKESSSTSTDEAAAGTVVLSEFMAERNKRFELAQVLANVGYWEYDRILQKITWSKHMYAIYGQALSSGVDLDNVFARVHEEDAGRVKLAFSNSLESMQSYQIEYRIIRPDGEVRYVAESARFWDNEAIGTVQDITEKTALQLQLIEEGQYYKSLFENNTDAVYSSNLEGMILSCNAAMNGLFGYTEGELVHASFERLIDPEQVSLSRKVIAEVINTVSPRSYELTARHKDGTAIDIFVTNIPVMIANELVGIYGIAKNVTEQKSMERHLLEAEAKYRSIVEQSIVGVFIVQNGIYIYANPHLERMLGNVNLMGRQVLDSIYPGDRDTVSTKMLGLTEGQFNRTMIHRAVKPDGSLIYCEVHYTRILHINEDAIVGTVLDITERKETEQETEYLAYHDYLTGLPNRRMFEEQLDQQLRLASFYNKKLAVLLIDLDRFKAVNDILGHTIGDTLLKQFAVKLQESLENGWVAYRLSGDEFCIILPEVESHREAIFLSESIISRTKEDYLIAGFELNITLSMGISIFPEDGDSVDRLLLNADSALYHAKSQGRDQAQCYSSSLNIQSFKIFTMTNDLRKALEKQELFLQYMPRVDTQTREILGAEALIRWNHPDWGLVSPAEFVPIAEESGLIVPIGEWVLREACRQNKQWQEMGLPHITVSVNFSVQQLFQQNILQTIDEILAGSGLAPEYLEIEITESSFMTNEREVIQLLEELRKRKIKVSLDDFGTGYSSLYMLKRLALDTVKIDKAFVEEILTDPVNQSIIECILNLAKALKMNVVAEGVETEAQYEYLKEQQCDEIQGYYFSRPVEQEALGMLLREKYIANPRPGVTEIPPVSNRREYFRVDLANPLVAGMTISTFKGREVDLGSTEVYLTNIGPGGLKFVMGYKLPVNDNILLKFETEILHQPTHLLGKIAWTHELENGAVYEYGVQFQMEESERLGLIRNLNNLAIQIREGTPAHTRIFLGDPVKSIKEQLKKVRL
>NZ_CP009280.1|WP_039294751.1|4839145_4839718_-|phosphate-propanoyltransferase
MSKTVSVGVSARHIHLTQEHVEALFGAGYQLTEFKPLSQPGQFAANEQVAVIGTKGKFDKVRILGPARPASQLEVSRTDAFSLGVKAPVRESGHIEGTPGITIKGPAGEVELETGVIVAARHIHFHTSEAEAWGIADKQLLKVRLGGERGLVLENVIARVSDNFKLDMHIDTDEANAAGANNGDTAEIVD
>NZ_CP009280.1|WP_144026167.1|4839872_4840847_-|membrane-dipeptidase
MRVADFHCDALSKLQASPEIDFKNDPRLDVTAERLVEGNVELQVFAVYLSADRGRAKFEDVLGQIELFRQKVVGPGGLQWLRWKEEADEQILTAPAFGMLSLEGVDGLEGNLFYAQLCFELGVRFLGVTWNYANWAADGVLEQRNGGFTEKGRKLIEWCNGSGMLLDVSHLAPAGFWELAERSKRPFIASHSNSAAICGHPRNLSDGQIQALIAVDGRMGLTFVPWFVRDGGGAKIDDMRRHIEHVCALGGSKQLMFGSDFDGIEMWVEGLEHPGKYAEFTDLLLRYYPEDEVKGWLCGNALTYLRTHLPSSAGVNPLSPPEGL
>NZ_CP009280.1|WP_019910496.1|4841083_4841344_-|stage-V-sporulation-protein-S
MDVLKVSAKSNPNSVAGALAGVLRERGSAELQAIGAGALNQAVKAVAIARGFVAPSGVDLICIPAFTDIVIDGEDRTAIKLIVEPR
>NZ_CP009280.1|WP_039294761.1|4841546_4842341_-|TIGR00282-family-metallophosphoesterase
MKVLFIGDIVGNTGRKALREMLPSLKSKYQPHIIIANGENAAAGRGITAAIANEFFNWGVHGITMGNHTWDNKDIFEFIDDEPRIIRPANFPPGTPGRGYTVVKGNGKQLAIVNLQGRTFLPAIDDPFRIGEEIVEELRREHKCILVDFHAEATSEKIAMGYFMDGLASIVVGTHTHVQSNDDVILPGGTAYLTDAGMVGSREGILGMEKDAIIYKFTTQLPSRFVVDEGKWQLHGLFAELDEATGKATRLEKIRLREDEWVMS
>NZ_CP009280.1|WP_039294762.1|4842602_4844144_-|ribonuclease-Y
METVIWVIIVLVVAAAFFGFGYFIRKSLAEAKISSAEKEAVVIVENAKKEAEALKKETVLEAKDEVHRIRTEAEKETRERRNEIQRQERRLLQKEESLDKKMESLERKEEQVANKEKRIDETQQQIDVIYKNQVTELERISNLSIDDARSIILSNVEQEVRHETAQMIKEIEQQAKEEADKKAREIITLAIQRCAADHVAETTVSVVTLPNEEMKGRIIGREGRNIRALETLTGIDLIIDDTPEAVILSGFDPIRREVARTALEKLVADGRIHPARIEEMVEKSRKEVDERIREYGEQATFEVGVHGLHPDLIKILGRLKFRTSYGQNVLKHSMEVAYLTGLMAGELGEDIVLAKRAGLLHDIGKALDHEVEGSHVEIGVELAKKYKEHPVVINSIASHHGDVEATSVIAMLVGAADALSAARPGARRETLETYIKRLEKLEEISESFEGVEKSYAIQAGREVRVMVQPEKIDDAEAFRLARDITKMIESELDYPGHIKVTVIRETRAVEYAK
>NZ_CP009280.1|WP_042138074.1|4844452_4845187_-|RecX-family-transcriptional-regulator
MVIQLDSEPDEQDVQILADFPEDEELVITRVERLKKSNYRYLIHFGAYNVTVHEDVMIKYRMISGSSFVKADLEEIVAADERQRAYVEGLKYLERKPRTAQEMARRLREKEIGETVIAEVLLRLQEERLLDDPLYAKQWAEQRITNQRKGKMWIRQELREKGIDKSLISEALDQITPEQEMESALQTGRKKWNLLRGDINEKRRKTGAFLMRRGFSGEMVRQVIQILRAEEDSAGEEVEIFDLD
>NZ_CP009280.1|WP_042138075.1|4845321_4846386_-|recombinase-RecA
MSDRRAALDMALRQIEKQFGKGSIMKLGESTHMKVEVVPSGSLALDIALGIGGLPKGRIIEVYGPESSGKTTVALHAIAEVQKLGGQAAFIDAEHALDPKYANALGVNIDELLLSQPDTGEQALEIAEALVRSGAVDIIVVDSVAALVPKAEIEGDMGDSHVGLQARLMSQALRKLSGAINKSNTIAIFINQLREKIGVMFGNPETTPGGRALKFYSSVRLDVRRVESIKMGNDVVGNRTKIKVVKNKVAPPFKQADVDIMYGEGISREGSLVDIGTEMDIVNKSGAWYSYEGERLGQGRENSKQFLKEHQDIALLIENKIREASNLSTLVAAPTEADVVAEQEEEEKLLLEIE
>NZ_CP009280.1|WP_042138077.1|4846671_4847961_-|competence/damage-inducible-protein-A
MKAEIIAVGTELLLGQIVNSNAQFLSIELAALGIDVYFQTVVGDNKNRLLEAIEIARNRADIILFTGGIGPTEDDLTKDALAAALGRTLHIDQLAMDHVQRFFDDRKIVMTENNRKQALVIEGTTPLSNEIGLAVGIAFAEDNKYYIVLPGPPREMKPMFTDKAKPWLQQHALTSEMPIYSKMLKFAGIGESLLEDKLIDLIRGQSDPTIAPYAKEGEVTVRISTKAPSEREAMVKLDVLEKKIADILPENLYANIDVPLEQLIVDWMADAGLTLSAAESCTGGLLMESITNIPGSASMFAGGIVCYSNDLKKKLLNVPAAMLEGPDAPGAVSREVAEVLAEQVRMIGDSDFGLSVTGVAGPGYSERKPVGLVFVGLAERGRKTEVYELNLKGTRENIRLRTVKALLYRLWRRLEERKVATPLEGSALQ
>NZ_CP009280.1|WP_039294770.1|4848020_4848608_-|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase
MNLPNRITLARICLIPIMMFFLLVDFSFYPEPIHWGSFQLSINHLIAAVIFLLAASTDGIDGYIARKYNMVTNLGKLLDPLADKLLVSAVLISLVELGRCDSWIAIVIISREFAVTGLRQVALLEGKVVAASKWGKIKTVTQIVAISLLLLNNFPFQFVSIPVDDIAIWAAAIITIYSGIDYFVKNKDLLQLHNA

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_CP009280_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_14

4842358-4842453

Orphan

Consensus_repeat	Method
AAGTTTTGTAAGCATCAGCTTCTTGGAAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_14

>merge|NZ_CP009280|14|4842358-4842453|CRISPRCasFinder
AAGTTTTGTAAGCATCAGCTTCTTGGAATTTTACTTCGTACAAAACTCGCATCGAAAGCATACTCTTAAGTTTTGTAAGCATCAGCTTTTGGAATA

>NZ_CP009280|14|12|4842358-4842453|CRISPRCasFinder
AAGTTTTGTAAGCATCAGCTTCTTGGAAT	TTTACTTCGTACAAAACTCGCATCGAAAGCATACTCTT
AAGTTTTGTAAGCATCAGCTTTTGGAATA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042138070.1\|4831752_4832649_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP009280.1\|WP_042138082.1\|4849730_4850690_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|224343
NZ_CP009280.1\|WP_042138072.1\|4834244_4835828_-\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223587
NZ_CP009280.1\|WP_042138071.1\|4832768_4833644_+\|4-hydroxy-tetrahydrodipicolinate-synthase	unknown	unknown	gnl\|CDD\|188637
NZ_CP009280.1\|WP_042138075.1\|4845321_4846386_-\|recombinase-RecA	unknown	unknown	gnl\|CDD\|236476
NZ_CP009280.1\|WP_039294751.1\|4839145_4839718_-\|phosphate-propanoyltransferase	unknown	unknown	gnl\|CDD\|237899
NZ_CP009280.1\|WP_144026167.1\|4839872_4840847_-\|membrane-dipeptidase	unknown	unknown	gnl\|CDD\|366534
NZ_CP009280.1\|WP_042138066.1\|4830551_4831004_+\|DNA-gyrase-inhibitor	unknown	unknown	gnl\|CDD\|225980
NZ_CP009280.1\|WP_042138080.1\|4848758_4849250_-\|YajQ-family-cyclic-di-GMP-binding-protein	unknown	unknown	gnl\|CDD\|213038
NZ_CP009280.1\|WP_042138074.1\|4844452_4845187_-\|RecX-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|237619
NZ_CP009280.1\|WP_042138087.1\|4852010_4852778_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|235506
NZ_CP009280.1\|WP_042138077.1\|4846671_4847961_-\|competence/damage-inducible-protein-A	unknown	unknown	gnl\|CDD\|234789
NZ_CP009280.1\|WP_019910496.1\|4841083_4841344_-\|stage-V-sporulation-protein-S	unknown	unknown	gnl\|CDD\|225234
NZ_CP009280.1\|WP_052421918.1\|4836001_4838950_-\|EAL-domain-containing-protein	unknown	unknown	gnl\|CDD\|236645
NZ_CP009280.1\|WP_036692667.1\|4851634_4851895_-\|DUF3243-domain-containing-protein	unknown	unknown	gnl\|CDD\|378681
NZ_CP009280.1\|WP_039294761.1\|4841546_4842341_-\|TIGR00282-family-metallophosphoesterase	unknown	unknown	gnl\|CDD\|379099
NZ_CP009280.1\|WP_042138068.1\|4831005_4831692_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293807
NZ_CP009280.1\|WP_039294770.1\|4848020_4848608_-\|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase	unknown	unknown	gnl\|CDD\|273139
NZ_CP009280.1\|WP_042138084.1\|4850719_4851487_-\|DUF3388-domain-containing-protein	unknown	unknown	gnl\|CDD\|314698
NZ_CP009280.1\|WP_039294762.1\|4842602_4844144_-\|ribonuclease-Y	unknown	unknown	gnl\|CDD\|237177

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042138070.1\|4831752_4832649_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	2.1738e-58
NZ_CP009280.1\|WP_042138082.1\|4849730_4850690_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|224343	COG1426, COG1426, Predicted transcriptional regulator contains Xre-like HTH domain [Function unknown].	3.99702e-33
NZ_CP009280.1\|WP_042138072.1\|4834244_4835828_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	6.19139e-160
NZ_CP009280.1\|WP_042138071.1\|4832768_4833644_+\|4-hydroxy-tetrahydrodipicolinate-synthase	gnl\|CDD\|188637	cd00950, DHDPS, Dihydrodipicolinate synthase (DHDPS). Dihydrodipicolinate synthase (DHDPS) is a key enzyme in lysine biosynthesis. It catalyzes the aldol condensation of L-aspartate-beta- semialdehyde and pyruvate to dihydropicolinic acid via a Schiff base formation between pyruvate and a lysine residue. The functional enzyme is a homotetramer consisting of a dimer of dimers. DHDPS is member of dihydrodipicolinate synthase family that comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways.	5.45284e-102
NZ_CP009280.1\|WP_042138075.1\|4845321_4846386_-\|recombinase-RecA	gnl\|CDD\|236476	PRK09354, recA, recombinase A; Provisional.	0
NZ_CP009280.1\|WP_039294751.1\|4839145_4839718_-\|phosphate-propanoyltransferase	gnl\|CDD\|237899	PRK15070, PRK15070, phosphate propanoyltransferase.	6.39357e-119
NZ_CP009280.1\|WP_144026167.1\|4839872_4840847_-\|membrane-dipeptidase	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	8.46948e-81
NZ_CP009280.1\|WP_042138066.1\|4830551_4831004_+\|DNA-gyrase-inhibitor	gnl\|CDD\|225980	COG3449, COG3449, DNA gyrase inhibitor [DNA replication, recombination, and repair].	1.53001e-39
NZ_CP009280.1\|WP_042138080.1\|4848758_4849250_-\|YajQ-family-cyclic-di-GMP-binding-protein	gnl\|CDD\|213038	cd11740, YajQ_like, Proteins similar to Escherichia coli YajQ. In Pseudomonas syringae, YajQ functions as a host protein involved in the temporal control of bacteriophage Phi6 gene transcription. It has been shown to bind to the phage's major structural core protein P1, most likely activating transcription by acting indirectly on the RNA polymerase. YajQ may remain bound to the phage particles throughout the infection period. Earlier, YajQ was characterized as a putative nucleic acid-binding protein based on the similarity of its (ferredoxin-like) three-dimensional topology with that of RNP-like RNA-binding domains.	1.42687e-87
NZ_CP009280.1\|WP_042138074.1\|4844452_4845187_-\|RecX-family-transcriptional-regulator	gnl\|CDD\|237619	PRK14135, recX, recombination regulator RecX; Provisional.	1.5185e-34
NZ_CP009280.1\|WP_042138087.1\|4852010_4852778_-\|SDR-family-oxidoreductase	gnl\|CDD\|235506	PRK05565, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	7.5676e-96
NZ_CP009280.1\|WP_042138077.1\|4846671_4847961_-\|competence/damage-inducible-protein-A	gnl\|CDD\|234789	PRK00549, PRK00549, competence damage-inducible protein A; Provisional.	0
NZ_CP009280.1\|WP_019910496.1\|4841083_4841344_-\|stage-V-sporulation-protein-S	gnl\|CDD\|225234	COG2359, SpoVS, Stage V sporulation protein SpoVS [Function unknown].	1.33023e-44
NZ_CP009280.1\|WP_052421918.1\|4836001_4838950_-\|EAL-domain-containing-protein	gnl\|CDD\|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	3.89296e-116
NZ_CP009280.1\|WP_036692667.1\|4851634_4851895_-\|DUF3243-domain-containing-protein	gnl\|CDD\|378681	pfam11588, DUF3243, Protein of unknown function (DUF3243). This family of proteins with unknown function appears to be restricted to Firmicutes.	1.19671e-39
NZ_CP009280.1\|WP_039294761.1\|4841546_4842341_-\|TIGR00282-family-metallophosphoesterase	gnl\|CDD\|379099	pfam13277, YmdB, YmdB-like protein. This family of putative phosphoesterases contains the B. subtilis protein YmdB.	5.29938e-155
NZ_CP009280.1\|WP_042138068.1\|4831005_4831692_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293807	cd07721, yflN-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis yflN; MBL-fold metallo hydrolase domain. This subgroup includes the uncharacterized Bacillus subtilis yflN protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	2.75718e-57
NZ_CP009280.1\|WP_039294770.1\|4848020_4848608_-\|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase	gnl\|CDD\|273139	TIGR00560, pgsA, CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase. Alternate names: phosphatidylglycerophosphate synthase; glycerophosphate phosphatidyltransferase; PGP synthase. A number of related enzymes are quite similar in both sequence and catalytic activity, including Saccharamyces cerevisiae YDL142c, now known to be a cardiolipin synthase. There may be problems with incorrect transitive annotation of near homologs as authentic CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase. [Fatty acid and phospholipid metabolism, Biosynthesis].	3.84608e-54
NZ_CP009280.1\|WP_042138084.1\|4850719_4851487_-\|DUF3388-domain-containing-protein	gnl\|CDD\|314698	pfam11868, DUF3388, Protein of unknown function (DUF3388). This family of proteins are functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 261 to 275 amino acids in length. This protein is found associated with pfam01842.	1.43434e-106
NZ_CP009280.1\|WP_039294762.1\|4842602_4844144_-\|ribonuclease-Y	gnl\|CDD\|237177	PRK12704, PRK12704, phosphodiesterase; Provisional.	0

>NZ_CP009280.1|WP_039294761.1|4841546_4842341_-|TIGR00282-family-metallophosphoesterase
MKVLFIGDIVGNTGRKALREMLPSLKSKYQPHIIIANGENAAAGRGITAAIANEFFNWGVHGITMGNHTWDNKDIFEFIDDEPRIIRPANFPPGTPGRGYTVVKGNGKQLAIVNLQGRTFLPAIDDPFRIGEEIVEELRREHKCILVDFHAEATSEKIAMGYFMDGLASIVVGTHTHVQSNDDVILPGGTAYLTDAGMVGSREGILGMEKDAIIYKFTTQLPSRFVVDEGKWQLHGLFAELDEATGKATRLEKIRLREDEWVMS
>NZ_CP009280.1|WP_019910496.1|4841083_4841344_-|stage-V-sporulation-protein-S
MDVLKVSAKSNPNSVAGALAGVLRERGSAELQAIGAGALNQAVKAVAIARGFVAPSGVDLICIPAFTDIVIDGEDRTAIKLIVEPR
>NZ_CP009280.1|WP_144026167.1|4839872_4840847_-|membrane-dipeptidase
MRVADFHCDALSKLQASPEIDFKNDPRLDVTAERLVEGNVELQVFAVYLSADRGRAKFEDVLGQIELFRQKVVGPGGLQWLRWKEEADEQILTAPAFGMLSLEGVDGLEGNLFYAQLCFELGVRFLGVTWNYANWAADGVLEQRNGGFTEKGRKLIEWCNGSGMLLDVSHLAPAGFWELAERSKRPFIASHSNSAAICGHPRNLSDGQIQALIAVDGRMGLTFVPWFVRDGGGAKIDDMRRHIEHVCALGGSKQLMFGSDFDGIEMWVEGLEHPGKYAEFTDLLLRYYPEDEVKGWLCGNALTYLRTHLPSSAGVNPLSPPEGL
>NZ_CP009280.1|WP_039294751.1|4839145_4839718_-|phosphate-propanoyltransferase
MSKTVSVGVSARHIHLTQEHVEALFGAGYQLTEFKPLSQPGQFAANEQVAVIGTKGKFDKVRILGPARPASQLEVSRTDAFSLGVKAPVRESGHIEGTPGITIKGPAGEVELETGVIVAARHIHFHTSEAEAWGIADKQLLKVRLGGERGLVLENVIARVSDNFKLDMHIDTDEANAAGANNGDTAEIVD
>NZ_CP009280.1|WP_052421918.1|4836001_4838950_-|EAL-domain-containing-protein
MNQKESSSTSTDEAAAGTVVLSEFMAERNKRFELAQVLANVGYWEYDRILQKITWSKHMYAIYGQALSSGVDLDNVFARVHEEDAGRVKLAFSNSLESMQSYQIEYRIIRPDGEVRYVAESARFWDNEAIGTVQDITEKTALQLQLIEEGQYYKSLFENNTDAVYSSNLEGMILSCNAAMNGLFGYTEGELVHASFERLIDPEQVSLSRKVIAEVINTVSPRSYELTARHKDGTAIDIFVTNIPVMIANELVGIYGIAKNVTEQKSMERHLLEAEAKYRSIVEQSIVGVFIVQNGIYIYANPHLERMLGNVNLMGRQVLDSIYPGDRDTVSTKMLGLTEGQFNRTMIHRAVKPDGSLIYCEVHYTRILHINEDAIVGTVLDITERKETEQETEYLAYHDYLTGLPNRRMFEEQLDQQLRLASFYNKKLAVLLIDLDRFKAVNDILGHTIGDTLLKQFAVKLQESLENGWVAYRLSGDEFCIILPEVESHREAIFLSESIISRTKEDYLIAGFELNITLSMGISIFPEDGDSVDRLLLNADSALYHAKSQGRDQAQCYSSSLNIQSFKIFTMTNDLRKALEKQELFLQYMPRVDTQTREILGAEALIRWNHPDWGLVSPAEFVPIAEESGLIVPIGEWVLREACRQNKQWQEMGLPHITVSVNFSVQQLFQQNILQTIDEILAGSGLAPEYLEIEITESSFMTNEREVIQLLEELRKRKIKVSLDDFGTGYSSLYMLKRLALDTVKIDKAFVEEILTDPVNQSIIECILNLAKALKMNVVAEGVETEAQYEYLKEQQCDEIQGYYFSRPVEQEALGMLLREKYIANPRPGVTEIPPVSNRREYFRVDLANPLVAGMTISTFKGREVDLGSTEVYLTNIGPGGLKFVMGYKLPVNDNILLKFETEILHQPTHLLGKIAWTHELENGAVYEYGVQFQMEESERLGLIRNLNNLAIQIREGTPAHTRIFLGDPVKSIKEQLKKVRL
>NZ_CP009280.1|WP_042138072.1|4834244_4835828_-|DEAD/DEAH-box-helicase
MTFNDLNLIPPILKALSLENYTSPTPIQEESIPAALAGRDILGCAQTGTGKTAAFSLPIIQLLSQQPARTGGAKRIRSLILTPTRELALQISENIQAYSKFTTIRSTAIVGGVSQKAQERALSQGADILIATPGRLIDLISQRHVDLQHVQILVLDEADRMLDMGFIHDVKRIIAKMPAKKQTLFFSATMPAEISQLVKTLLVDPVKIEITPVSSTVDRIEQSIYLLENGNKQNQLNRLLQDPSIVSALVFTRTKRGADRVTRDLTRINITAQAIHGNKSQNDRQNALRNFKSGATRVLVATDIAARGIDIDELSHVINFNLPNIPETYVHRIGRTGRAGMSGVAISLCEAEEIPYLKDIQKLIGKVIPEVKDHAYPMSKSNLALLADRPGKAPAKPSQKAKTNPARKPKSEWFSQGKQGGGNGGAKSASGSGYAGSGAKSASGSGYAGNGAKSASGSSYAGSGAGSSRPAGESGNRAGSGSRPGERSAARPGGNRSSKPAGGQYGRSSQSGNRPGNRPAAKAGRSQ
>NZ_CP009280.1|WP_042138071.1|4832768_4833644_+|4-hydroxy-tetrahydrodipicolinate-synthase
MLTEEQIYGIYVPVVTPFHAAGEIDLESYQRYVNNIIKNSIHGLVVNGTTGESPTVNIQELQTLVDASRELLKNTSIPLVVGTGTNDTMSTVTRTELAANSGADAALVVVPYYSRPSQEGIIAHFRKAAEVGLPIIAYDIPGRAGVGMSVDTARTILEMNNVVGLKDCSGSPVLVSELSRHGSKPVLCGDDLNFFDMLGCGAAGGMLASANVHTASYLSIYEQYRAGQVEAARAAFDQLVPLMKLLFKESNPAPIKWLLSARGEISSDTLRLPMTSISAALREELGAYLAG
>NZ_CP009280.1|WP_042138070.1|4831752_4832649_-|LysR-family-transcriptional-regulator
MDLTYMRTFREVAKRQSFTRAAEELGYAQSSVTMQIQKIEKEYGVPLIERHGRALRLTPPGEELLKLFVEILDLYDRSKETIAQQIGGTLTIGTIDSLAAFYLPPFLQQLRTMFPGLNIHLQTEQEANLVSKIRDGEVDIGLLLDRSTADILLERTIIREEPLVLVAPASHPLASVAQVTLQDLNNCELIVSEESCIYRSLFENLLREHGIVFRIGFELSNLEAIKRCVRNGLGIALLPRIVAEEEIERGNLAELSFAHPEIHFDLQLLLHPKKWKSLPLQSLIQMLREDAKAKAAIL
>NZ_CP009280.1|WP_042138068.1|4831005_4831692_-|MBL-fold-metallo-hydrolase
MDIIELPIQFEYEGQPYYIYPSLIVSGEELTLVDTGYPTFMPLIEKKILELGYDPLNLKNIIITHYDDDHIGALYEFVEKYPSVTVMASEVDTPSISGLVKSERLVQAEALLVEMPKEEQASGEEFVQLLKNLRHVPVKQTVREGQCILDGKCQVLATPGHTSGHISLYFPELSSVITGDAAVSEENELAVANPQYCFDLESAEQSLNRLQALNARSYYCYHGGKLGF
>NZ_CP009280.1|WP_042138066.1|4830551_4831004_+|DNA-gyrase-inhibitor
MKIQLQTLPVTRIAYVRQTGPYGPGNSKAMGALKEWARAHRLLTGSAILFGIPQDNPDTTLPEHCRYDACISVLENAPADKSINYGEIPGGTYAVVTIQHTAEAVQKAWTEILPALYVSGHQLDYQRPVMERYTGDMISNHLCQLCFPVH
>NZ_CP009280.1|WP_039294762.1|4842602_4844144_-|ribonuclease-Y
METVIWVIIVLVVAAAFFGFGYFIRKSLAEAKISSAEKEAVVIVENAKKEAEALKKETVLEAKDEVHRIRTEAEKETRERRNEIQRQERRLLQKEESLDKKMESLERKEEQVANKEKRIDETQQQIDVIYKNQVTELERISNLSIDDARSIILSNVEQEVRHETAQMIKEIEQQAKEEADKKAREIITLAIQRCAADHVAETTVSVVTLPNEEMKGRIIGREGRNIRALETLTGIDLIIDDTPEAVILSGFDPIRREVARTALEKLVADGRIHPARIEEMVEKSRKEVDERIREYGEQATFEVGVHGLHPDLIKILGRLKFRTSYGQNVLKHSMEVAYLTGLMAGELGEDIVLAKRAGLLHDIGKALDHEVEGSHVEIGVELAKKYKEHPVVINSIASHHGDVEATSVIAMLVGAADALSAARPGARRETLETYIKRLEKLEEISESFEGVEKSYAIQAGREVRVMVQPEKIDDAEAFRLARDITKMIESELDYPGHIKVTVIRETRAVEYAK
>NZ_CP009280.1|WP_042138074.1|4844452_4845187_-|RecX-family-transcriptional-regulator
MVIQLDSEPDEQDVQILADFPEDEELVITRVERLKKSNYRYLIHFGAYNVTVHEDVMIKYRMISGSSFVKADLEEIVAADERQRAYVEGLKYLERKPRTAQEMARRLREKEIGETVIAEVLLRLQEERLLDDPLYAKQWAEQRITNQRKGKMWIRQELREKGIDKSLISEALDQITPEQEMESALQTGRKKWNLLRGDINEKRRKTGAFLMRRGFSGEMVRQVIQILRAEEDSAGEEVEIFDLD
>NZ_CP009280.1|WP_042138075.1|4845321_4846386_-|recombinase-RecA
MSDRRAALDMALRQIEKQFGKGSIMKLGESTHMKVEVVPSGSLALDIALGIGGLPKGRIIEVYGPESSGKTTVALHAIAEVQKLGGQAAFIDAEHALDPKYANALGVNIDELLLSQPDTGEQALEIAEALVRSGAVDIIVVDSVAALVPKAEIEGDMGDSHVGLQARLMSQALRKLSGAINKSNTIAIFINQLREKIGVMFGNPETTPGGRALKFYSSVRLDVRRVESIKMGNDVVGNRTKIKVVKNKVAPPFKQADVDIMYGEGISREGSLVDIGTEMDIVNKSGAWYSYEGERLGQGRENSKQFLKEHQDIALLIENKIREASNLSTLVAAPTEADVVAEQEEEEKLLLEIE
>NZ_CP009280.1|WP_042138077.1|4846671_4847961_-|competence/damage-inducible-protein-A
MKAEIIAVGTELLLGQIVNSNAQFLSIELAALGIDVYFQTVVGDNKNRLLEAIEIARNRADIILFTGGIGPTEDDLTKDALAAALGRTLHIDQLAMDHVQRFFDDRKIVMTENNRKQALVIEGTTPLSNEIGLAVGIAFAEDNKYYIVLPGPPREMKPMFTDKAKPWLQQHALTSEMPIYSKMLKFAGIGESLLEDKLIDLIRGQSDPTIAPYAKEGEVTVRISTKAPSEREAMVKLDVLEKKIADILPENLYANIDVPLEQLIVDWMADAGLTLSAAESCTGGLLMESITNIPGSASMFAGGIVCYSNDLKKKLLNVPAAMLEGPDAPGAVSREVAEVLAEQVRMIGDSDFGLSVTGVAGPGYSERKPVGLVFVGLAERGRKTEVYELNLKGTRENIRLRTVKALLYRLWRRLEERKVATPLEGSALQ
>NZ_CP009280.1|WP_039294770.1|4848020_4848608_-|CDP-diacylglycerol--glycerol-3-phosphate-3-phosphatidyltransferase
MNLPNRITLARICLIPIMMFFLLVDFSFYPEPIHWGSFQLSINHLIAAVIFLLAASTDGIDGYIARKYNMVTNLGKLLDPLADKLLVSAVLISLVELGRCDSWIAIVIISREFAVTGLRQVALLEGKVVAASKWGKIKTVTQIVAISLLLLNNFPFQFVSIPVDDIAIWAAAIITIYSGIDYFVKNKDLLQLHNA
>NZ_CP009280.1|WP_042138080.1|4848758_4849250_-|YajQ-family-cyclic-di-GMP-binding-protein
MSSESSFDIVSKMDMQELTNAVHQTEKEIDNRFDFKNSKSSLKLEKDALIIASEDEYKLNAVIDILQSKMVKRGITLKNMDFGKVEPASLGTVRQRLGLKQGIDQENAKKINILIRDSKLKVKSTIQGDQIRVTGKSRDDLQQIIQLLRKADLPLDLQFNNLK
>NZ_CP009280.1|WP_042138082.1|4849730_4850690_-|helix-turn-helix-domain-containing-protein
MSELGRHLKEARLQKGMSLDDVQEVTKIRKKYLEAIEAGDYKVLPGSFYVRAFIKTYAEAVGVNPDELMEEHGNVPAAPVDTTMETVIQKRSRKPETERNAKWLPTLLMWTFPVLILVVIYLYASSTMNKEEADKTDSGSLTAATQDPAKVQPSATAAGGGAAATATTDTGATATVAPTATPVPSPTPSTQSITVTEDRKSGKTTIYKVTAPAGSSVQVEIAATGVSWLEVYQGENSKGEKLSFGNTKAGDNMSFTLGSAGMYIKSGYSPATTISVNGQVITDGKTSSRLLLELDDGTSASGTDDAANAASDGESATTE
>NZ_CP009280.1|WP_042138084.1|4850719_4851487_-|DUF3388-domain-containing-protein
MEYKQWYMEYKIHKNRPGLLGDIASMLGMLEVNILTINGVEGKTRGMLLETSDDEKIMLMGEMLKKVDNITVTALRSPRLVDKLAVRHGRYIDRDSDDRKTFRFTRDELGLLVDFLGELFKREGNQVIGLRGMPRVGKTESIIAGSVCAMKRWTFVSSTLLRQTVRSQLADDELNPNNVFIIDGIVSTIRSNEKHYNLLQNVMSMPSTKVIEHPDIFVRESEYTFDDFDIIIELRNTPNEEILYESFTTSYSDDL
>NZ_CP009280.1|WP_036692667.1|4851634_4851895_-|DUF3243-domain-containing-protein
MSTDSVVKNFDTWKSFLGDRVIQAEKMGMSDETITKLAFEIGEFLDKKVDPGNYSNRAIKELWDVGTDDEKHTIAGLMVKLAKKNA
>NZ_CP009280.1|WP_042138087.1|4852010_4852778_-|SDR-family-oxidoreductase
MALPGEGSKAIGEMTVLITGGSGGIGGAIAERFASVGMNIVIHYMNSHEAANDVARRCMALGAKVMTVAADMKDRSQLVRMAERLEASGMMPDILVNNAGKAHYGMLADVTEEEWDDIMAVNLKGTFMCSQIFMPYMVSQRYGRIINVSSVWGISGASCEVAYSASKGGVNAFTKALAKELAPSKVTVNAVAPGAVQTAMLANLQADEVKMLEDEIPAGRLASPEDISSLVYFLALPESGYITGQIISPNGGWIT

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_CP009280_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_15

5255324-5255410

Orphan

Consensus_repeat	Method
GTTTTGATAGCATATGCTGCTTGAT	CRISPRCasFinder

1 spacers

DinG

The CRISPR arrays of NZ_CP009280_15

>merge|NZ_CP009280|15|5255324-5255410|CRISPRCasFinder
GTTTTGATAGCATATGCTGCTTGATTCAACTTCGCAAAACTCGCTTCGTAAGCATTCACTTAGGTTTTATAGCATATGCTGCTTGAT

>NZ_CP009280|15|13|5255324-5255410|CRISPRCasFinder
GTTTTGATAGCATATGCTGCTTGAT	TCAACTTCGCAAAACTCGCTTCGTAAGCATTCACTTA
GGTTTTATAGCATATGCTGCTTGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042138599.1\|5259256_5259640_-\|aspartate-1-decarboxylase	unknown	unknown	gnl\|CDD\|376751
NZ_CP009280.1\|WP_042138591.1\|5251736_5252504_-\|DUF4111-domain-containing-protein	unknown	unknown	gnl\|CDD\|379178
NZ_CP009280.1\|WP_042138589.1\|5249173_5250676_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273520
NZ_CP009280.1\|WP_052421944.1\|5261710_5262511_-\|biotin--[acetyl-CoA-carboxylase]-ligase	unknown	unknown	gnl\|CDD\|223417
NZ_CP009280.1\|WP_042138603.1\|5265104_5265809_-\|bacillithiol-biosynthesis-deacetylase-BshB1	unknown	unknown	gnl\|CDD\|274915
NZ_CP009280.1\|WP_042138594.1\|5253364_5254666_-\|amidohydrolase	unknown	unknown	gnl\|CDD\|238623
NZ_CP009280.1\|WP_042138596.1\|5255525_5258384_-\|ATP-dependent-DNA-helicase-DinG	DinG	COG1199_DinG_CAS-IV-A	gnl\|CDD\|236148
NZ_CP009280.1\|WP_042138582.1\|5244855_5245623_-\|DnaD-domain-containing-protein	unknown	unknown	gnl\|CDD\|226445
NZ_CP009280.1\|WP_042138584.1\|5245646_5246942_-\|asparagine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235176
NZ_CP009280.1\|WP_042138601.1\|5263854_5265012_-\|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA	unknown	unknown	gnl\|CDD\|274914
NZ_CP009280.1\|WP_042138600.1\|5259632_5260523_-\|pantoate--beta-alanine-ligase	unknown	unknown	gnl\|CDD\|376824
NZ_CP009280.1\|WP_042138598.1\|5258500_5259142_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP009280.1\|WP_039309895.1\|5265808_5266231_-\|methylglyoxal-synthase	unknown	unknown	gnl\|CDD\|179969
NZ_CP009280.1\|WP_042138587.1\|5248168_5249041_-\|3-hydroxybutyryl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|180269
NZ_CP009280.1\|WP_042138586.1\|5246963_5248172_-\|acetate-kinase	unknown	unknown	gnl\|CDD\|234680
NZ_CP009280.1\|WP_039308791.1\|5260524_5261391_-\|3-methyl-2-oxobutanoate-hydroxymethyltransferase	unknown	unknown	gnl\|CDD\|234723
NZ_CP009280.1\|WP_039308806.1\|5254652_5255306_-\|redox-sensing-transcriptional-repressor-Rex	unknown	unknown	gnl\|CDD\|235486
NZ_CP009280.1\|WP_042138590.1\|5250668_5251211_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379491
NZ_CP009280.1\|WP_042138593.1\|5252815_5253334_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227656
NZ_CP009280.1\|WP_052421945.1\|5262500_5263844_-\|CCA-tRNA-nucleotidyltransferase	unknown	unknown	gnl\|CDD\|237339

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042138599.1\|5259256_5259640_-\|aspartate-1-decarboxylase	gnl\|CDD\|376751	pfam02261, Asp_decarbox, Aspartate decarboxylase. Decarboxylation of aspartate is the major route of beta-alanine production in bacteria, and is catalyzed by the enzyme aspartate decarboxylase EC:4.1.1.11 which requires a pyruvoyl group for its activity. It is synthesized initially as a proenzyme which is then proteolytically cleaved to an alpha (C-terminal) and beta (N-terminal) subunit and a pyruvoyl group. This family contains both chains of aspartate decarboxylase.	1.3767e-82
NZ_CP009280.1\|WP_042138591.1\|5251736_5252504_-\|DUF4111-domain-containing-protein	gnl\|CDD\|379178	pfam13427, DUF4111, Domain of unknown function (DUF4111). Although the exact function of this domain is not known it frequently appears downstream of the family Nucleotidyltransferase, pfam01909. It is also found in species associated with methicillin-resistant bacteria.	1.85099e-36
NZ_CP009280.1\|WP_042138589.1\|5249173_5250676_-\|AAA-family-ATPase	gnl\|CDD\|273520	TIGR01241, ATP-dependent_zinc_metalloprotease_FtsH, ATP-dependent metalloprotease FtsH. HflB(FtsH) is a pleiotropic protein required for correct cell division in bacteria. It has ATP-dependent zinc metalloprotease activity. It was formerly designated cell division protein FtsH. [Cellular processes, Cell division, Protein fate, Degradation of proteins, peptides, and glycopeptides].	1.76454e-147
NZ_CP009280.1\|WP_052421944.1\|5261710_5262511_-\|biotin--[acetyl-CoA-carboxylase]-ligase	gnl\|CDD\|223417	COG0340, BirA, Biotin-(acetyl-CoA carboxylase) ligase [Coenzyme metabolism].	4.63954e-83
NZ_CP009280.1\|WP_042138603.1\|5265104_5265809_-\|bacillithiol-biosynthesis-deacetylase-BshB1	gnl\|CDD\|274915	TIGR04001, thiol_BshB1, bacillithiol biosynthesis deacetylase BshB1. Members of this protein family are BshB1 (YpjG), an enzyme of bacillithiol biosynthesis; either BshB1 or BshB2 (YojG) must be present, and often both are present. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	1.09303e-93
NZ_CP009280.1\|WP_042138594.1\|5253364_5254666_-\|amidohydrolase	gnl\|CDD\|238623	cd01298, ATZ_TRZ_like, TRZ/ATZ family contains enzymes from the atrazine degradation pathway and related hydrolases. Atrazine, a chlorinated herbizide, can be catabolized by a variety of different bacteria. The first three steps of the atrazine dehalogenation pathway are catalyzed by atrazine chlorohydrolase (AtzA), hydroxyatrazine ethylaminohydrolase (AtzB), and N-isopropylammelide N-isopropylaminohydrolase (AtzC). All three enzymes belong to the superfamily of metal dependent hydrolases. AtzA and AtzB, beside other related enzymes are represented in this CD.	0
NZ_CP009280.1\|WP_042138596.1\|5255525_5258384_-\|ATP-dependent-DNA-helicase-DinG	gnl\|CDD\|236148	PRK08074, PRK08074, bifunctional ATP-dependent DNA helicase/DNA polymerase III subunit epsilon; Validated.	0
NZ_CP009280.1\|WP_042138582.1\|5244855_5245623_-\|DnaD-domain-containing-protein	gnl\|CDD\|226445	COG3935, DnaD, Putative primosome component and related proteins [DNA replication, recombination, and repair].	4.87632e-39
NZ_CP009280.1\|WP_042138584.1\|5245646_5246942_-\|asparagine--tRNA-ligase	gnl\|CDD\|235176	PRK03932, asnC, asparaginyl-tRNA synthetase; Validated.	0
NZ_CP009280.1\|WP_042138601.1\|5263854_5265012_-\|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA	gnl\|CDD\|274914	TIGR03999, thiol_BshA, N-acetyl-alpha-D-glucosaminyl L-malate synthase BshA. Members of this protein family are BshA, a glycosyltransferase required for bacillithiol biosynthesis. This enzyme combines UDP-GlcNAc and L-malate to form N-acetyl-alpha-D-glucosaminyl L-malate synthase. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	0
NZ_CP009280.1\|WP_042138600.1\|5259632_5260523_-\|pantoate--beta-alanine-ligase	gnl\|CDD\|376824	pfam02569, Pantoate_ligase, Pantoate-beta-alanine ligase. Pantoate-beta-alanine ligase, also know as pantothenate synthase, (EC:6.3.2.1) catalyzes the formation of pantothenate from pantoate and alanine.	2.7273e-160
NZ_CP009280.1\|WP_042138598.1\|5258500_5259142_-\|hypothetical-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	0.000488048
NZ_CP009280.1\|WP_039309895.1\|5265808_5266231_-\|methylglyoxal-synthase	gnl\|CDD\|179969	PRK05234, mgsA, methylglyoxal synthase; Validated.	1.73553e-76
NZ_CP009280.1\|WP_042138587.1\|5248168_5249041_-\|3-hydroxybutyryl-CoA-dehydrogenase	gnl\|CDD\|180269	PRK05808, PRK05808, 3-hydroxybutyryl-CoA dehydrogenase; Validated.	6.91387e-109
NZ_CP009280.1\|WP_042138586.1\|5246963_5248172_-\|acetate-kinase	gnl\|CDD\|234680	PRK00180, PRK00180, acetate kinase A/propionate kinase 2; Reviewed.	0
NZ_CP009280.1\|WP_039308791.1\|5260524_5261391_-\|3-methyl-2-oxobutanoate-hydroxymethyltransferase	gnl\|CDD\|234723	PRK00311, panB, 3-methyl-2-oxobutanoate hydroxymethyltransferase; Reviewed.	1.21978e-155
NZ_CP009280.1\|WP_039308806.1\|5254652_5255306_-\|redox-sensing-transcriptional-repressor-Rex	gnl\|CDD\|235486	PRK05472, PRK05472, redox-sensing transcriptional repressor Rex; Provisional.	2.83546e-109
NZ_CP009280.1\|WP_042138590.1\|5250668_5251211_-\|hypothetical-protein	gnl\|CDD\|379491	pfam14155, DUF4307, Domain of unknown function (DUF4307). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 132 and 153 amino acids in length. There is a single completely conserved residue C that may be functionally important.	0.00992337
NZ_CP009280.1\|WP_042138593.1\|5252815_5253334_-\|hypothetical-protein	gnl\|CDD\|227656	COG5353, COG5353, Uncharacterized protein conserved in bacteria [Function unknown].	1.84344e-17
NZ_CP009280.1\|WP_052421945.1\|5262500_5263844_-\|CCA-tRNA-nucleotidyltransferase	gnl\|CDD\|237339	PRK13299, PRK13299, tRNA CCA-pyrophosphorylase; Provisional.	1.07142e-124

>NZ_CP009280.1|WP_039308806.1|5254652_5255306_-|redox-sensing-transcriptional-repressor-Rex
MKSDKISEAVVRRLPVYLRFLNDLQKREISTVSSQELGQKLDLNPAQIRKDLAYFGDFGRKGIGYDVSYLIEKIRHILKLDQQINVALVGAGNLGHALSNYNAYLKDTMKITAVFDAYEPKVGQQINSLTVQPMSELGDTIRAQGIRIGIITVPDSEAQNVADILVDSGIEAILNFAPVILKTPANIRIHAADFTTDLQSLAYYLHDGKDEAEDEQQ
>NZ_CP009280.1|WP_042138594.1|5253364_5254666_-|amidohydrolase
MSSNKTIIKNGRFLVPGSDKPVLSGYMTIENDLITYIGEDKPVIEEDAEVIDGSRLLFMPGLVNTHGHAAMSLLRGYGDDMVLQAWLQEKMWPMEEKFTGDDVYWGTSLSVLEMLKGGTTTFLDMYDHMDRVAEVTEQSGIRAVLMRGVIGLCPEEVQNHKLAEAIAFARNWHGKADGRITAMLSPHAPYTCPPEFFMKFVQAAHDLDLPMHTHMSETRHEVEQNVADYGLRPVAHLEKLGMFTRPSLIAHGVHLNDEEIEILARHNVGVSHNPGSNLKLASGVARVPELLRAGVKVSLGTDGAASNNNLDMFEEMRLAALIHKGVSGDPTAVPAPEALLMATEYGAQSIFLNQVGRLAAGMKADFIAIDIDQPHLLPHTDLLSHAVYSASAKDVENVWVNGKQVVKHGQCLTLDEEAIRRKAQETFEGLLKR
>NZ_CP009280.1|WP_042138593.1|5252815_5253334_-|hypothetical-protein
MKKRRKWLPLGISLVLLLLFGLSQFYAYIMKDQWNERSEAKEIARARAGLTEVTKAQKSVWDENAIYWVLTGKNDAGTELMVWVRFTKEGQPAGGDNDLYAEELSKGTSEAQIRDIIAAQLPGITIKRLLPGVYNGEYAWQLFYKKDGRFYYSFYRFTDGSAIGEGYSLPNR
>NZ_CP009280.1|WP_042138591.1|5251736_5252504_-|DUF4111-domain-containing-protein
MEILAYLDQAVTLFKEELGANLSGIYLHGSLAMGCFHPDKSDIDLLIVVHDKLPVEVSRKLAKKVIAYHDSLPNRRGVELTIVLKKYLKNFVHPTPFEFHFSDFHLDRYRNDEHYLCGGFEDRDLAAQFAVVYQRGFILYGEPIREAFLPVDRQYYLDSILGDIGDAAQQIIDSPVYYTLNLCRVLYFVREEVVSSKKEGGEWGLQHLPSSYHGLLKHCLEEYSGVASDSSYDPELLIDFAEYMAGEIRQHQAKV
>NZ_CP009280.1|WP_042138590.1|5250668_5251211_-|hypothetical-protein
MKLRLMPVLLTSLLSAALLFGGWYSYRQFAVQEPLQKLVSSYEGVKDSHISIKRNEVTLKLDLQPGTKLRELVQYVSKEGSSAINGRTLKLDVEQNSSALLDEYWDKAMFSVAEAMESRKYTLIPAKLDGLKTQDSKYSGVIATTEIDDKNVYVSLSNGKESKFIILPRAAATMGVWNNA
>NZ_CP009280.1|WP_042138589.1|5249173_5250676_-|AAA-family-ATPase
MPKYWKEVLAGFVPVMLIFMVFVGINIFPVIIAFGMVAALLFIAHARGGLAVNAGADKKRKKNGPSKLTFEEIGGQDNAKQELREALDFLIRHEEISKFGIRPLKGILLTGPPGTGKTLMAKAAAHYTNSVFVAASGSEFVEMYVGVGAGRVRDLFKDARTRALKENKQSAIIFIDEIDVIGGKREGGQQREYDQTLNQLLTEMDGIYNNEAPRILLVAATNRKEMLDSALLRPGRFDRHIQVDMPDKKGRKSILDLHAKNKPLHETVSLDKIAEEAYGFSGAQLESVMNEAAIYMMRENLTQVEQRHLSMAIDKVMMGEKTDRETNHEEKQRVAIHELGHAIMAELLRPGSVSQVTLTPRGQALGYVRHNPQTEQYLYTKDYLENQIMIALGGAAAEEMYYGGRSTGSRGDFDQALNIVETMMKSGLTSLGIANLQMVTTEELMKENSKILDELMVRTNDLLNKQRNVFDYSLDILMKEEVLSGEQFRCQFRDSVLLPA
>NZ_CP009280.1|WP_042138587.1|5248168_5249041_-|3-hydroxybutyryl-CoA-dehydrogenase
MNFKKIGVIGGGTMGQGIAEMLAAKGLDVMLVEKTADRLNYSYEMIETSLDKQLEKWAITQAEKKLILSRIQKVTHFAELSSCDMVIETIVEDLEAKQKVFNQLDQVCPSHIILASNTSTLSLTELASSTMYPERVIGMHFIHPVAKVDLVEIVRGLKTSDSTFEDTKTFVDEIVEKKGVMIYESPGFVTSRLICLFINEAMHVLQEGVASPEDIDDAMRIGYQFQNGPLEMADRFGLDSVLAALENMFREYGELKYRPSTILKKMVRAGQLGAKSGEGFFKYDKDGDRV
>NZ_CP009280.1|WP_042138586.1|5246963_5248172_-|acetate-kinase
MNILVINSGSSSLKYQLYNMTDESVLAKGLVERIGMDSSILNHKPTGKQEVTEVSEILEHNTAIRKVLACLTDKEHGVIASTDEINAVGHRVVHGGEFFKASALVDADAKTKIRQLFDLAPLHNPAAMMGITATEINMPGVPQVVVFDTAFHQTMPEKAYMYAIPRVLYNKYKVRRYGAHGTSHDFVSKAAADYLDRPLGELKIITCHIGNGASVTAVDGGVSVDTSMGMTPLEGLMMGTRSGDLDPAIVPYVMNKEELSVGEVNSMLNKHSGLLAISGVSSDMRDIIDGAEKGEANSTLAFEMYEYRLRKYIGSYAAAMNGVDVIVFTAGVGENASLLREKVLNNLTFLGIELDAEANKVRSGDPRRISTPGSKVQVLVVPTNEELVIARDTYSIVQGING
>NZ_CP009280.1|WP_042138584.1|5245646_5246942_-|asparagine--tRNA-ligase
MANKSVIKNVNEHVGESVVIGCWVNNKRSSGKIQFLQLRDGTGYIQGVVVKSEVPEQVWDDAKSLTQESSLYVTGIIREEPRSQSGYEMTVTGIEVLHLTENYPITPKEHGVDFLMDHRHLWLRSSKQRAVMVIRAEIIRAVQQFFNESGFTKVDPPILTPTSAEGTTNLFHTKYFEEDAYLTQSGQLYMEAAAMALGRVYSFGPTFRAEKSKTRRHLIEFWMIEPEMAFTDHEESLRVQEDFISFVVQSVLTNCRAELEAVGRDVSKLENIKAPFPRISYDDAIKFLNEKGYEIAWGDDFGAPHETAIAEMSDKPVFITHYPASFKAFYMKPHPERPEVVLCADMIAPEGYGEIIGGSQRIDDPALLEARFKEHNLSMDTYKWYMDLRTYGSVPHSGFGLGLERTVAWICGLDHVRETIAFPRTLYRLYP
>NZ_CP009280.1|WP_042138582.1|5244855_5245623_-|DnaD-domain-containing-protein
MDGKGWNTWGEGVAFGLENGMAVIPYALLKYYRKLNLTGSEAMLLIHLLSFRQVEGIDFPSLEELQAVTGRSISVIAGELQKLMKEGFISIDGDNDELRDIHYERYNFSGLYGKLGAYLAEVSQEHSQEKRSRAESEPGSRAAAHYSGSPAPEGGYGRPAAPGGTEAEESRSLFSIFEKEFGRPLSPMECESISGWVDEDRYPEELILLALKESVFAGKVHFRYIDRILLEWARNRVKNAQDVKAYSQKFRSGGR
>NZ_CP009280.1|WP_042138596.1|5255525_5258384_-|ATP-dependent-DNA-helicase-DinG
MKFAVLDFETTGTQSVGEIIQVGLAIIEEDRSISRVYGSYVKPGAPIPPFITGLTGITDSDVQDAPELDEMMMELVPLLDDVVLVGHNVAFDFHFLQNALDRCGYLPFQGRILDTIDFLKICFPSLTTYQLGSVSSHFGLTHERPHQADSDALATALVLLKCLEELDSLPLLTIQRLNELFADEDSDLAWYFDGLQREREMETFQPEGDLTFYRQLALAVGDWAELAPPREEGSDNPLQNITFGEYMEEVTKRLKDTLPQYESREAQELMIQEVMTALDQDKHLLIEAGTGTGKSLGYLLPAIYHSVRSNQKVMVSTHTINLQDQLRERDIPLLTSVVPFPFKAAIFKGRGHYLCLRKFEHRINKRDFTSPREEALTAAQMMVWLTQTETGDDEELNLSGRGGDFWETVASDTDSCLGRSCPWFRKCYYHRAKHEAGISDVVVTNHSKLFADVKAGHQLLPAYEHLIIDEAHHLEDIAGKHLGMQMKYFTVAHTLTRLYKDSRSGQLPALRQTLQSSGSEQASEWSGVIDRIYPDLLTVKESWDTLSDKLFGLLPERSDAGAGEAGQLVARLQPGKKPKEWEELAALENTLHLSLSDIIRKGDKMLSEMRDTDSQSSSDSLVTDIGGLFKDLASIREQIRFFMGLNDENIVYWLEGSGNYRGKSLQMYAVPVDVSTQLRELFFDKKKSIILTSATLSVDKSFQFMIDNLGLGEAAEQGRLMTALLPSPFKYREQALLVIPRDFPSVKGSIGDARFVDTLVHSLAETAVATRGRMLVLFTSYKMLRQVYDPLKEALASQDIAVLGQGVEGGSRSKLIRRFQDSTASVLLGTSSFWEGVDIPGEALTCLAIVRLPFQPPNHPLAEAKSELLQAQKKNPFMKLSVPQAVIRFKQGFGRLVRTAQDRGIVIVYDTRVIESYYGKYFLYSLPGPKMEHMLTDQIVPRIAEWLEEGGV
>NZ_CP009280.1|WP_042138598.1|5258500_5259142_-|hypothetical-protein
MFQHLFAEMNKMLQEISADYPTAEGARRNDLLSKYNMLHRISDDVMDEWLAFAEKLSQFRNQADFQPQPEQEIPEEEAPELAMDAFVRGQGYYKLLMYRKCIEQFKEVTARHPDSLAARLYLAMAYLQEGEGETAWGHLNHMLGLIRETKLKAMIYNALGCIRASQERFNEASELFSLSLLHDPALPEPNINLEVCRKRGGKLQFGQQLVSLL
>NZ_CP009280.1|WP_042138599.1|5259256_5259640_-|aspartate-1-decarboxylase
MFRHMMKSKIHRATVTEANLNYVGSITIDENLMEAADLLENEKVQIVDNNNGSRLETYVIPGPRGSGVICLNGAAARLVQPGDTVIIISYAMLSSEELADHKPTVVFVDAGNQPVKLADHEIHATIA
>NZ_CP009280.1|WP_042138600.1|5259632_5260523_-|pantoate--beta-alanine-ligase
MRVIRTIAQLREALEYMRQGGHGPVGFVPTMGYLHEGHASLLRAAGEKSGTVVMSIFVNPLQFGPNEDYASYPRDEQRDLALAEREGADIVFIPSVEEMYPQPIRTGVSVSSLTTQLCGASRPGHFDGVTTVVSKLFNIVQPDYAFFGLKDAQQVAVLRRMVADLNMNVEIIACPIVREEDGLALSSRNVYLSAEERRQALVLSRSLREVRQALENGKVRTVEEARALLVSVIAESPLAVIDYAEILTFPDLESLEGGGKLSAAGGEVIMALAVKFGRTRLIDNNVFIPKEAHALV
>NZ_CP009280.1|WP_039308791.1|5260524_5261391_-|3-methyl-2-oxobutanoate-hydroxymethyltransferase
MAEKHPLNIIKMKKMKTEGVPLSMLTAYDYPSALLAEEAGVDLILVGDSLGNVVLGYDTTLPVTIDDMVYHTRSVKRGAQNTFIIADMPFMTYHGSVDETLRGVRRLMQEGQAHAVKMEGGLEICNAVSAVVAAGVPVLGHIGLTPQSVNMIGGYRIQGKDAKDAQRLIDEAKALEAAGAFGIVLELVTEEVAAAISKAISIPTIGIGAGRYCDGQVLVFHDVLRYASPYREKRFVKTYADVGSLIREGISSYVREVKDRSFPAEEHVFNADETVLESLYGGAGKGAK
>NZ_CP009280.1|WP_052421944.1|5261710_5262511_-|biotin--[acetyl-CoA-carboxylase]-ligase
MKSDDTLPSGRMKREDFVSSWPGEIVRMDSVASTQEEAKKLAENGAPEGTAIMAEEQTGGRGRMGRKWHSPRGKGIWMSLVLRPNLPLSLTPQLTLLAGVAVCTAIREVTGVPAGIKWPNDLLAGGRKICGILLESSLREGGLHYCIAGIGIAVNLTREDYPAELQEVGTSLLIEGGGIPVDRTGLAEAVLAELEYLYLQYIEQGFRPIRELWESMSVTLGRQVCVNTPQGRTEAMAVGLDDNGGLRLRNSAGEITSVLSGEIEMI
>NZ_CP009280.1|WP_052421945.1|5262500_5263844_-|CCA-tRNA-nucleotidyltransferase
MEWTMASSGMAEAAGTVITGLLAGGHEAYFVGGCLRDELLGRPVHDMDITTSALPEEVMALFPRCVPTGLAHGTVTVLQNGYSFEVTTYRTESGYADHRRPEHVFFVSDVKEDLRRRDFTINAMCSGLNGALIDPFGGERDLQLRRIRCVGQAEERFGEDALRMLRCVRFASVLDFAIAKNTWRGLMRQRDKLAHIAVERVRAEVERIVEGPHPQRGLALLLRSGLLPRGKAPFPWTGSDLAAAAARTAGLGNLQDARLRWALLLHALGSSAAAADELLRAWTFPGATRSSVVAVLRVREAWDAALSSVAPDAPGATEGLRRRWIAAVLAHGQSAAEGWLTLLAAAEDALGPAATVPPVLSPAAGQQPVYATVQARILRSWTAAMPLRSLAELAVTGNELAELLQKRPGPWLGVLLNKLLLAAAAGGIANDKQLLLQEAQRMDRDEE
>NZ_CP009280.1|WP_042138601.1|5263854_5265012_-|N-acetyl-alpha-D-glucosaminyl-L-malate-synthase-BshA
MDRLKIGITCYPSLGGSGVVATELGKLLAEKGHEVHFITHSIPFRLGTFQKNIFYHEVEVNDYYVFRYPPYDLALATKMAQVAKMQKLDLFHVHYAVPHAVCAFLAKQILGNDIKVVTTLHGTDITVLGQDESLKDLIRLGINESDAVTAVSQDLIKETRKALDITREIDLTYNFVDKRVYYPRDVTDLRGDYAAPDEKILMHISNFRPVKRVSDVVDVFAKVNKHLPSRLLLVGEGPDLPKIQAKISEMGLEDKVRFLGKQDEIAQVISLADLLLLPSEKESFGLVALEAMACGVPTIGSQTGGIPELIQHGKTGFLAPVGDTQTMADYAVQLLSDDAMAESFRRACLERACHDFSRDMITNQYEDIYYRVLGRKVLGLDPIRG
>NZ_CP009280.1|WP_042138603.1|5265104_5265809_-|bacillithiol-biosynthesis-deacetylase-BshB1
MKLDILVFGAHADDAEIGMAGTIAKHTAAGFKVGMCDLTQAEMSSNGTVELRKLEAQQAADMLGAAVRTNLGLPDRGLYMTEHHLAAVTAEIRRYAPSIVFAPYWEDRHPDHIACSKLVEEAVFNAKLRKYMPDMPSIPEPQLYFYFINDLGRTDLIVDVTEQYPLKEQALSCYRSQFGILPGEDAVKTPLTEGYIERVRSRDMLLGQRRLIPYAEGFAGKVPHTVDYFGAAGK
>NZ_CP009280.1|WP_039309895.1|5265808_5266231_-|methylglyoxal-synthase
MLKIAFIAHDRKKDEMVNFVTAYEHVFEGHQLYSTGTTGQRIMEATKLVIHRYMSGPLGGDQQIGSMVATDELDLIIFLRDPLMAQPHEPDITALLRLCDVYGIPVATNIATAEILVKAIDRGDFGWRELVHKYKPGVDE

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_CP009280_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_16

5751194-5751289

Orphan

Consensus_repeat	Method
TTGCTTCGTACAAAACTCGCTTCGAAAGCATA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_16

>merge|NZ_CP009280|16|5751194-5751289|CRISPRCasFinder
TTGCTTCGTACAAAACTCGCTTCGAAAGCATATGCTTAAGTTTTGATAGCATAACCTTCCTAATTTGCTTCGTACAAAACTCGCTTCGGAAGCATA

>NZ_CP009280|16|14|5751194-5751289|CRISPRCasFinder
TTGCTTCGTACAAAACTCGCTTCGAAAGCATA	TGCTTAAGTTTTGATAGCATAACCTTCCTAAT
TTGCTTCGTACAAAACTCGCTTCGGAAGCATA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042138901.1\|5756595_5758194_+\|response-regulator	unknown	unknown	gnl\|CDD\|381091
NZ_CP009280.1\|WP_052421981.1\|5746925_5747705_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|227095
NZ_CP009280.1\|WP_156118681.1\|5754662_5756444_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|225519
NZ_CP009280.1\|WP_042138899.1\|5749140_5751150_-\|beta-galactosidase	unknown	unknown	gnl\|CDD\|367090
NZ_CP009280.1\|WP_156118682.1\|5764135_5764285_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138896.1\|5744646_5745264_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138900.1\|5751301_5752126_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_042138894.1\|5742524_5743871_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340863
NZ_CP009280.1\|WP_042138903.1\|5762069_5762951_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|212492
NZ_CP009280.1\|WP_042138902.1\|5758480_5761324_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379757
NZ_CP009280.1\|WP_081970081.1\|5745341_5745779_+\|DUF4362-domain-containing-protein	unknown	unknown	gnl\|CDD\|372994
NZ_CP009280.1\|WP_052421982.1\|5753106_5754453_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270452
NZ_CP009280.1\|WP_042138895.1\|5744113_5744635_+\|matrixin-family-metalloprotease	unknown	unknown	gnl\|CDD\|239806
NZ_CP009280.1\|WP_039306468.1\|5752138_5753029_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP009280.1\|WP_042138897.1\|5745862_5746510_-\|elongation-factor-G-binding-protein	unknown	unknown	gnl\|CDD\|319974
NZ_CP009280.1\|WP_042138904.1\|5763309_5763816_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138893.1\|5741137_5742349_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP009280.1\|WP_042138898.1\|5747732_5749070_-\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|307945
NZ_CP009280.1\|WP_042138892.1\|5739024_5740776_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270300
NZ_CP009280.1\|WP_042141419.1\|5761455_5761953_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042138901.1\|5756595_5758194_+\|response-regulator	gnl\|CDD\|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.02368e-55
NZ_CP009280.1\|WP_052421981.1\|5746925_5747705_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.70051e-27
NZ_CP009280.1\|WP_156118681.1\|5754662_5756444_+\|HAMP-domain-containing-protein	gnl\|CDD\|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.73491e-62
NZ_CP009280.1\|WP_042138899.1\|5749140_5751150_-\|beta-galactosidase	gnl\|CDD\|367090	pfam02449, Glyco_hydro_42, Beta-galactosidase. This group of beta-galactosidase enzymes belong to the glycosyl hydrolase 42 family. The enzyme catalyzes the hydrolysis of terminal, non-reducing terminal beta-D-galactosidase residues.	6.22459e-81
NZ_CP009280.1\|WP_042138900.1\|5751301_5752126_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	6.62057e-71
NZ_CP009280.1\|WP_042138894.1\|5742524_5743871_+\|MFS-transporter	gnl\|CDD\|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	8.06754e-60
NZ_CP009280.1\|WP_042138903.1\|5762069_5762951_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|212492	cd05327, retinol-DH_like_SDR_c_like, retinol dehydrogenase (retinol-DH), Light dependent Protochlorophyllide (Pchlide) OxidoReductase (LPOR) and related proteins, classical (c) SDRs. Classical SDR subgroup containing retinol-DHs, LPORs, and related proteins. Retinol is processed by a medium chain alcohol dehydrogenase followed by retinol-DHs. Pchlide reductases act in chlorophyll biosynthesis. There are distinct enzymes that catalyze Pchlide reduction in light or dark conditions. Light-dependent reduction is via an NADP-dependent SDR, LPOR. Proteins in this subfamily share the glycine-rich NAD-binding motif of the classical SDRs, have a partial match to the canonical active site tetrad, but lack the typical active site Ser. This subgroup includes the human proteins: retinol dehydrogenase -12, -13 ,and -14, dehydrogenase/reductase SDR family member (DHRS)-12 , -13 and -X (a DHRS on chromosome X), and WWOX (WW domain-containing oxidoreductase), as well as a Neurospora crassa SDR encoded by the blue light inducible bli-4 gene. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.78894e-61
NZ_CP009280.1\|WP_042138902.1\|5758480_5761324_-\|hypothetical-protein	gnl\|CDD\|379757	pfam15979, Glyco_hydro_115, Glycosyl hydrolase family 115. Glyco_hydro_115 is a family of glycoside hydrolases likely to have the activity of xylan a-1,2-glucuronidase, EC:3.2.1.131, or a-(4-O-methyl)-glucuronidase EC:3.2.1.-.	7.85314e-168
NZ_CP009280.1\|WP_081970081.1\|5745341_5745779_+\|DUF4362-domain-containing-protein	gnl\|CDD\|372994	pfam14275, DUF4362, Domain of unknown function (DUF4362). This family of proteins is found in bacteria. Proteins in this family are typically between 93 and 146 amino acids in length. There is a conserved IRIV sequence motif.	1.99523e-17
NZ_CP009280.1\|WP_052421982.1\|5753106_5754453_-\|extracellular-solute-binding-protein	gnl\|CDD\|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	8.00549e-55
NZ_CP009280.1\|WP_042138895.1\|5744113_5744635_+\|matrixin-family-metalloprotease	gnl\|CDD\|239806	cd04279, ZnMc_MMP_like_1, Zinc-dependent metalloprotease; MMP_like sub-family 1. A group of bacterial, archaeal, and fungal metalloproteinase domains similar to matrix metalloproteinases and astacin.	9.99988e-07
NZ_CP009280.1\|WP_039306468.1\|5752138_5753029_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.94698e-69
NZ_CP009280.1\|WP_042138897.1\|5745862_5746510_-\|elongation-factor-G-binding-protein	gnl\|CDD\|319974	cd16342, FusC_FusB, Fusidic acid resistance protein (FusC/FusB). The fusidic acid resistance protein FusC (FusB) mediates resistance to the antibiotic fusidic acid. Its C-terminal domain, which contains a zinc-binding site, interacts with EF-G with high affinity, promoting the dissociation of stalled ribosome#EF-G#GDP complexes that form in the presence of fusidic acid, thus allowing the ribosomes to resume translation.	2.49061e-90
NZ_CP009280.1\|WP_042138893.1\|5741137_5742349_-\|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.	2.92567e-12
NZ_CP009280.1\|WP_042138898.1\|5747732_5749070_-\|glycosyl-hydrolase	gnl\|CDD\|307945	pfam02055, Glyco_hydro_30, Glycosyl hydrolase family 30 TIM-barrel domain.	2.46237e-44
NZ_CP009280.1\|WP_042138892.1\|5739024_5740776_+\|extracellular-solute-binding-protein	gnl\|CDD\|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	0
NZ_CP009280.1\|WP_042141419.1\|5761455_5761953_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	3.68181e-16

>NZ_CP009280.1|WP_042138899.1|5749140_5751150_-|beta-galactosidase
MDHLLYGVAYYDEYMPYDRLDEDIRMMQEAGINTVRIAESTWSTHEPQNGVFNFSPVTRVLDAMHAAGIHVIVGTPTYAIPAWMVKEHPDVLAVTAQGEGKYGARQIMDITHPVYLFYAERIIRKLMAVVHKHPAVIGYQIDNETKHYETAGPNVQLKFVKYMRETYGTLEAINQRFGLDYWSNRIDSWEDFPSMVGTINGSLGAEFARFQRGLVNEFLAWQIGIVGEYKQPGQFTTHNFDFEWRGHSFGVQPSVDHFAAAAPFDIAGVDIYHPSQDNLTGTEISFGGDMTRSLKQDNYFVLETQAQAFPEWTPYPGQLRLQAFSHIGSGASMVAYWHWHSIHNSFETYWKGLLSHDFLPNPVYKEARTIGADFKRLSDRLIGLKKTSKVAVMVSNEALSAIEWFKLPGGVIYNDVVRWMYDELYKMNIACDFIQPSCTRLSDYELIVVPALYAVSDEALQRLNEYVRSGGHAVYSFKSGFTDEQVKVRHTAQPGVIHEACGVAYSHFATPNASAGLTGKLFPEGTEAGVHTVRTWMEMLVPDSAEVLASYDHPQWGEYAAVTRNSFGDGTATYIGCMTEPAALAVILRDTLQVAGLWGEDQQLSFPLIVKSGVNRHGSTIRYYYNYSAESVTFQYPHGAGQELLSGNPVAHAEELKLEAWGVFIISED
>NZ_CP009280.1|WP_042138898.1|5747732_5749070_-|glycosyl-hydrolase
MDVKDIVWVSSTESEPWVSRSVESAAAEGAADLAFTREIHQNIEGFGGCFNELGFEALNLLAAEDRSAVLHSLFHPEGDHKFSICRLPIGASDYALEWYSLNETDGDYAMEHFSIERDRKYLIPYIREALKLNPELKLFASPWSPPTWMKFPRAYNYGTLRWEKEILEAYALYFVKFVQAYAGEGITIHQVHVQNEVVADQKFPSCVWTGEQLREFIRDYLGPAFEQRGLDTEIWLGTINAPEPWDEWMKQKDSGFDAYAHTVLSDPEAYKYVQGVGYQWAGKYGIQRTVQAYPELRYMQTENECGDGENTWFYAKYVFNLYQHYFTNGVNAYIYWNMVLQPKGRSTWGWEQNSMITVDPDEPKAVHNPEFYVMKHFAHFIGPGSRRIGLKGRWTGNALAFGTPEGRRVLVIANPFKEARTILLANDETHYKLMLDAESFNTLIL
>NZ_CP009280.1|WP_052421981.1|5746925_5747705_+|helix-turn-helix-domain-containing-protein
MDIHKYEHLVPDVFLFVDRRSFADWEIISSTIDFHDLSFIVEGKADYFINGEKFTVEAGDMLYVPSGSVREAHTFAEAPMHSFAFNFFWTGADNHVHLPFETVTKHRMTKEILDDIREFSHNWMGGQPFYRMKARAIFQLIVYRLLNITHHQETPLLDPRIHKVMAYIMDHYAEEVTIKALAEWIGLNPVYLGKLFKQNTGSTCKEFLNRVRVNNAEMILSAGGFNVSEVAEHCGYHDVAYFSNVFKSMKGYPPSAALK
>NZ_CP009280.1|WP_042138897.1|5745862_5746510_-|elongation-factor-G-binding-protein
MTTTFIRNHQYNYIKKQSDFVLKTLRSVADRRVLETVRYSAEVNVTEAFSSLTTEQEQMLKPISTLEKAEDFQQYISGFEPYLEPFPPITLKQIQKLFPKNKKMKLPDLASFDFRYVTYLAWADIATNKLFIVYPYEGQFIGVEGRIIPTHKKGYCLFCNRQQDLAFLTVKTKPELASADNIASVGQYVCIDNHGCNQSITNISSLERFVLSVQK
>NZ_CP009280.1|WP_081970081.1|5745341_5745779_+|DUF4362-domain-containing-protein
MEGYRMKMLRVCIYMLLMSLIIVACSNSMHYEAAAKKGYVVYVQGEIINYTYFEQFVENYNNGQDATVKIAKYTDEGDPIFHTLEYKRDQKKISYTYDNSEDENGDKLQANTLCSSITNVDGVYHLADCADDETGKWFSAKQPSK
>NZ_CP009280.1|WP_042138896.1|5744646_5745264_+|hypothetical-protein
MRKFRNKYFYSIITVVLLLGVVMVVNDNKTLTNAESSYNKTDNVTDKVTSTASPKEVVEYHGDLAENFNTVSKLTYGSDAIYEVEVNDSKSFEYEGVIFTVSNANVNEHYKGGSIDTVNILETGGNYNNTEYVFEDSSVLKIGDKAIVYLEKYEGPIPEAQGTYVVTGAYQGKFEIDEANGSLIPAAVDQEELKEVRALTDLNLE
>NZ_CP009280.1|WP_042138895.1|5744113_5744635_+|matrixin-family-metalloprotease
MKKIAPIVCTLLIFFAVLPSSTFAYTYSANANPFPDMNFTYYSILSANYSGPAAAAMNDWAGAVGASYTAVAPTYNEIQFSDNDYGNTGWNAETSHHHVNFSSYDYLDEVRANRYYMGSMSAVTREGVFGHELGHVFGLGHTTNTWTLMCTFEDGRVVVTPQLDDIQGVQSLY
>NZ_CP009280.1|WP_042138894.1|5742524_5743871_+|MFS-transporter
MSEPTPVSAASNRNIILFFSGKFASVLGSSMYTFVVGLYILQLTGSGSSFAVTLLCGMLPSIILSPFAGVVADMVNRRKLLIGSDAASVLIMLLSFAAVSIEGMSLLPIYISLILLSICATFYSISASSSMMMLVDRDSIQRTGSLNQIASSVGHLLAPILAGMLYAFLPLEEFMLLNAAGLTISTVMGCMLKFKPAPEALSEARLTDGPAETGNPPFRERLGNVAAEVRTNLKEGFSYVIRRPVIRSLLIIVFWINFFVVALNIVLPFVAVQTLGLSSKQYGILEAMLAAGMLLMSLLLTVLRQSNNPVNTIIGGLGALGLLFLAMALPLLLHFTAAVTFFFFLPLLILVGVVIMIINIPIQVYLQQSIEEEYRGRVFGLVEGIAGSIAPLGMLLYGVLLDWIPGSIILLASGAAILAVTLIGRRGLISSNADEQQGIHAEVEQAGA
>NZ_CP009280.1|WP_042138893.1|5741137_5742349_-|helix-turn-helix-transcriptional-regulator
MTTKLTIGDKVKQMRKAKGLTQTDLAGEHMTKSMLSQIENGRALPSMNTLQFLAGRLGTDAGYFLEGEHEAELGPLVRKIEQQYKAKQYKEIVAEIQPLMKDTLPMAVDAARLMEFYVGSCYHTGTEGGEEGIERAVEIYERFGLFVERAKIQYLAYALMFAKSRYQDGLELIRRVRKEYVSNKVGNDFLFEIDLYYAESVTLSALADYSGSREAALAALKLSHEEGVYSLSDHLYRLLSHLALLHNDLEQAEAYLSKAKLFAQFTEAAESLELVHLGEIRLALAKQSYGEVLTLAENYPAKDSQFMPFVHMMTGTALYHLERDEEALADLSKVVLNDQVYHPLDRVDLLTAYAYKAKIFAKQGLMEEARYEVELAYDQVKDYPPSEYADLIRQTYHELYNAQ
>NZ_CP009280.1|WP_042138892.1|5739024_5740776_+|extracellular-solute-binding-protein
MTRKTAKPYVALMVLTLLLSVLAGCGGGNNNSKNTAGNTGTEATNSTNAAATAEATAAAEDLSPLTLSFFAEDPNPNWNNMKDEVSTVLTEKTGVTLDAEFAVGDPQQKIALIAAGGEYPDIISAKADIGKLVDAGAVIDLTELIDKYAPNIKRVLGDNLARAKYTNEDQSIYAIPTWAAVNEKKFVAGGGFELQHRVLKEAGYPEIKTVQDYENVIKAYLEKHPTDENGNKNIGVSLNADDWHMYISVTNPAVATTGGSDDGEYFIDQETHEAIYHFRRPEEKEYFRWLNHMNDIGLLDKESFVQKYDQYKAKVATGRVLGLIDQDWDYNDAQQALKTAGKFDQTYGHYPVTLTSEYKETSFWPTGFMGGYGISISTTNPDPVRTIKFLDYLASDEGQILNNWGIEGKHYVVENGKRVVPAEVQDRINNDNTAFTKETGIGFYWNMMVHYGDGAKDSTGNYYTKNFPEQLVLGYSDVEKETLAAYNATTWKDLFPKEEEFAEKAYGAAWNIALPGEDEVSILGNKMRDITWKRIPQAILAKPAEFDKIWDDYMADLEKAGVKKMEAGYTKYVQDRVELWSAK
>NZ_CP009280.1|WP_042138900.1|5751301_5752126_-|carbohydrate-ABC-transporter-permease
MTKSTKTILWVFFLFVALVQLFPLIWLLDFSFLSSNEFYSSSILKWPSAPQWQNYINAWVDGKFLRYFINSAFITTVTILLTVVLSLTLGYAFTRMDWKFRSVFFTIILLGIMIPIHATLLPNFAIFKALGLTDSYLGLILPYTAVSVPMGTFILTGFLRSIPKALEESAIVDGANIYRIVFQIIAPLTAPALVTVVVTTFLNCWNEFIMASTFLSKDALKTLPFSVMNFAGQYSSDYGSQFAVMVLTSIPAIVIYAIFNEQITKGVTAGAVKG
>NZ_CP009280.1|WP_039306468.1|5752138_5753029_-|sugar-ABC-transporter-permease
MQKVFNNKMAIFLFVFPGILLFSLTFLVPIVLSGYYSFRDTLAPGTPSAFIGFANYTELLFHDTRFWLALRNAVLLGLGFIFIQHPIAIFFAIMLDRLGGKAEKWFRTIFFIPCVISVVVISKMWLSLLDPTFGAFNKLLDTLGLGFLKHAWLGDSSTALVTMLFILIWAGFGWGLLFYYAGLKGIPDEMYEAASLDGASGFKLHLRITVPLLSPVITVQITLAMITALKQMETVFLTTNGGPGDSTQFLAVYLYNKAFSASQYGYANAISILFIVVCLLATYLSNKLTRSDATEF
>NZ_CP009280.1|WP_052421982.1|5753106_5754453_-|extracellular-solute-binding-protein
MVMNTKATRNLLLITALAAVSVLSACGGNDQNESAGSTNGNAADPAAEQVTLRVFSNLPDRKSGQGLAEQMVIDNYTKENPNVKIELETLAEEPFKNKLKAYMASNEALDITMVHGGAELNTLVQAGYVKELDPAGYEGETYNFLPGVYKSFTFNDKLYGLPRNSDYEVIYYNQKIFADNGVNVPATYAELLDAAKQFRDKGIEPMSVNGKDLWSFAAFFQDLVIRVSGDQSLMLDAVEQKKNFTTDESFITAAKLLGEARDAKLFQESFMTADYGASQNLFTQGKAAMWYMGSWEAGMATNESLSEDFRNNVAVLKFPVVDGGKGKDTDLLAWNGGGYSLVSSSKHPEEAKKFFDYLMRADQWAKTVWDTGAAVPAQKYELTGTESGLQKQLTDVLTGATTTAGSLGLDYGTPKFKDDGQNAFGKFFAGGSTPEELLADLQKAAESQ
>NZ_CP009280.1|WP_156118681.1|5754662_5756444_+|HAMP-domain-containing-protein
MNLRYKITILIFLLITAVTFAIGGYSYTISKKQIINKVSNSNQSVLKQIDSNLSRMQKTIADWVTVFSLASVVQETLRSNTPDSVEIEDQFYNGPTASMMNQMLVTGNFDYLALYGSLSAPMFQVATDDSSGAYSLDKITPHNIYKESVALNGASYWFPLTEENNVFIQSNRNDKLGMTRIIRDIVNGNRIGFVFVGINLETIRRTYLTDLYDQDHGILILNESGKQLLAAGKETYDKKAVDFVMKRAEAGILSGYTIVNLQGGDTLLNYNINANGWITLYSVPLSSLTEELNSIKSAVLIMILASLLLSIPLLMFFSSFLTAPIKTLLLSMRRFQNGQFEEKVNIKYWDEIGQLSRGYNNMVANIKALVDDAYLLKLKEQEAELKALQSQINPHFLYNMLDTIFWEAEAAGQDKISEMVINLSRLFRLSLNQGKSFTSVAKEKELIELYLSLQKMRFKDSLDFVIDIPDELHPYVILKLSLQPFIENALIHGIERKRGGGCVSISGQRTGDQLMFVIEDNGGGMSSETLQKILTLPDESDIYTARDTGGYAVQNVQARLKHFYKGDFTLHYTSVPGEGTRVEIIIPAILNDI
>NZ_CP009280.1|WP_042138901.1|5756595_5758194_+|response-regulator
MFNMIIVDDEERARVGIRTLIDWQAHGITIVAEARDGQEALDILSIHPVDIMLTDIRMPQMDGLELISIVSGKYPHIKSVIMSGYDDFAYAQQAIRVGASNYLLKPSRRQEILNTILDITEQIQSEKLEIKSLEHLRQGFRESLPLLKEKTLSQLVLTESPAYPQLLANLKMNNLIFPYLLYGVILLRIDNFRQLHQKYLHEDTELLKYGLKNICEESLPETIVCIAFEHQDDIVLILNTDELLDHEELSGYIRIIQDNILSYLRFTVSAGIGSIDKNLQHLRRSFLEASQALNTRNYTGTGKIVEFSGEFDDEASQSSYPLHEEQEVLKAVRNGSPEEIAGKLTLFNVALQPETVSRDQVIKSSFALFFALYKLCIENNVNVNKVFGQNLTELIQVLSRSSLDHIFQSLLETALLVSEHLTSKKNSNKLLEAAKLYIGQNYMKDINREIVAREIYITPGYLSLLFKQQLKISFTDYLHKIRIEHACLLFKDPGMRIEDIALQSGYNDTKYFYQVFKKYKGITPNQFRSNAE
>NZ_CP009280.1|WP_042138902.1|5758480_5761324_-|hypothetical-protein
MKSNEDFILAAPDQAVQIYLDPKGTDYNGLRRVAESFGADIELVSGIAPVILTRKEQLSGTVVIAGAIGGNELIDRLITEGALDVTSIQGKRECYRLQLVEAPMPGVDRALVIAGSDKRGTIYGIYSISELIGVSPWVYFADVVPEQNTTLSIPVSRLNRSTREPSVKYRGFFLNDDWPSLGSWVTHAFGDFNEGFYDKVFELILRLKGNFLWPAMWSAEFSLNGTSSPIANAVHADEYGIVMGTSHHEPLFRAGSEWQKVYAQYGTSNLWDFARNPQAITAFWEDGIKRNRHYDNLVTLGMRGESDSALEGSDQENIELLKQIILTQKALLKKYNLEHMPQVLAVYKEVEKYWYGTAEAEGLKDWEVLQDVTILLSDDNFGNLRKIPEKHEQQREAGWGIYYHFDYHGGPHSYEWVNVTPLEKVWEQMTMAFDYGIRDIWVVNAGDLKPMELPLSYFMDLAYDFEAWGTGAINQTEEYTRRWVEQQFGSDLTPGTVDGIAQVLADYTRMNGRRKPEIIRAGTFSLLHHQEAQRVLEQALSLEQAAARYESELPAALKDAYYQLVYYPAVASANVVKMQIYAGLNRLHAGRGSVLANTYADLVLESIERDKQLEQHYNTGISDGKWQGMMSSPHVGYVNWNADGWSYPEVSRVTPAKEAIMIVGVEGTEQGYTAGTAGLTPFTNLQQETYEITVSSGGAGFGYKAVRSAEWIRLDRTQGWVDTGAAIRVSVDWEKVQGAASGHITLSGAGTIVTVQVEVEWTDITNVPPMTFIETQNTVSIEAEHTLNRVAKSGAEWKTINNYGRTLSSVKMFPAGSSFDQPEEAPCLEYRLLVHQDGEYSLTAYIAPTNQLSPVRGLKYAAGFDGEPPVTADALPPGYEGGNHDNEPWCRAVMDNIHTQVTRHVLAKGQHTLRFYGLDAGLVLQKLVLSAGPLPYSYLGPVESYHS
>NZ_CP009280.1|WP_042141419.1|5761455_5761953_-|MarR-family-transcriptional-regulator
MKQNPINDIQVNNEPINIDQSRLDSREQLELALGEQLNALISAAHALNVKAAARFDSSLQPAAFHIVRWLYSYGPASAAAIAEATAMDRSAVSRQIKQLESLGYVSREASPDDGRAILLSLTEQGQQQTIAALNEKGSVFFGRTAAWKDDELHQFIHMLKQFNGL
>NZ_CP009280.1|WP_042138903.1|5762069_5762951_+|SDR-family-NAD(P)-dependent-oxidoreductase
MPKQPTVVITGATSGLGQLVAIQLAERGYALVLTARSEERAAATRTIIEARQPAANIRFVYGDLSLMQDVNRVGAEIAAACPSIDVLLNNAGIHAFEPRTTAEGLPEMMAVNYLAPWLLTHRLETSLRNAGQARVVNVASEASRRHGVLRLPGDLTDTAAFTARGSSPVYGKTKLLNIMFTAELARQWAGSGITVNALNPGFNVTGLGRELRFASVIERILKIVRLGDPRRGAEIITRLIVDPHYGAVTGGYFNVGTGKSIVPVSPGGDEAMQRRLWADTRELLGEILGENRD
>NZ_CP009280.1|WP_042138904.1|5763309_5763816_+|hypothetical-protein
MKNTKKIIIGFISLIIVLAVFYGGYFKNNKEIEFFHDKFGIPLPKESKLIYSYKSYGALGDGYRLYIYQVTSKSMNDIVKKGHANHWSELPLPSDFTASFSKKIRAITDETTSKLITLDAARGYYMIRNNQTNASITGTNVFNSSFDNVMIGIMNLDNNRIYLLSYNM
>NZ_CP009280.1|WP_156118682.1|5764135_5764285_-|hypothetical-protein
MFKKIYLIALALTIISGVALISNSKAGSYPEMVTANKTDKNPVNTNFSE

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_CP009280_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_17

5872375-5872519

Orphan

Consensus_repeat	Method
AGTGGCAACGGCATCGGGAACGACG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP009280_17

>merge|NZ_CP009280|17|5872375-5872519|CRISPRCasFinder
AGTGGCAACGGCATCGGGAACGACGGCATGGGCACCAGCGGGAATGGCGACAGCGACACCAGCGGCAACGGCATCGGGAACGACGACAGCAGTGGCAGCGGGAACGACAGCGGGAACGGCGGCAGCAGTGGCAGCGGGAACGGCG

>NZ_CP009280|17|15|5872375-5872519|CRISPRCasFinder
AGTGGCAACGGCATCGGGAACGACG	GCATGGGCACCAGCGGGAATGGCGACAGCGACACC
AGCGGCAACGGCATCGGGAACGACG	ACAGCAGTGGCAGCGGGAACGACAGCGGGAACGGC
GGCAGCAGTGGCAGCGGGAACGGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_156118686.1\|5886072_5886228_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138956.1\|5863365_5863641_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042141438.1\|5875768_5878060_-\|glycoside-hydrolase-family-65-protein	unknown	unknown	gnl\|CDD\|224471
NZ_CP009280.1\|WP_042141433.1\|5857044_5857728_+\|pectate-lyase	unknown	unknown	gnl\|CDD\|367395
NZ_CP009280.1\|WP_042138951.1\|5857830_5858502_+\|SOS-response-associated-peptidase	unknown	unknown	gnl\|CDD\|376837
NZ_CP009280.1\|WP_042138955.1\|5861738_5862056_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_081970086.1\|5873789_5875091_-\|DUF4432-family-protein	unknown	unknown	gnl\|CDD\|379620
NZ_CP009280.1\|WP_042138963.1\|5875080_5875821_-\|beta-phosphoglucomutase	unknown	unknown	gnl\|CDD\|213672
NZ_CP009280.1\|WP_042141443.1\|5880051_5881359_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270452
NZ_CP009280.1\|WP_042138960.1\|5866410_5866623_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224393
NZ_CP009280.1\|WP_052421987.1\|5858554_5859595_-\|fibronectin-type-III-domain-containing-protein	unknown	unknown	gnl\|CDD\|238020
NZ_CP009280.1\|WP_042138965.1\|5883541_5885164_+\|response-regulator	unknown	unknown	gnl\|CDD\|381091
NZ_CP009280.1\|WP_156118684.1\|5863665_5864070_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138961.1\|5866750_5866945_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042138958.1\|5864471_5865173_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_081970087.1\|5881716_5883549_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|225519
NZ_CP009280.1\|WP_156118685.1\|5885189_5886089_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|378940
NZ_CP009280.1\|WP_042138964.1\|5878924_5879800_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP009280.1\|WP_039308352.1\|5878079_5878904_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_042138959.1\|5865552_5866329_-\|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223528

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_052421987.1\|5858554_5859595_-\|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.	0.000254501
NZ_CP009280.1\|WP_042141438.1\|5875768_5878060_-\|glycoside-hydrolase-family-65-protein	gnl\|CDD\|224471	COG1554, ATH1, Trehalose and maltose hydrolases (possible phosphorylases) [Carbohydrate transport and metabolism].	0
NZ_CP009280.1\|WP_042141433.1\|5857044_5857728_+\|pectate-lyase	gnl\|CDD\|367395	pfam03211, Pectate_lyase, Pectate lyase.	4.20903e-70
NZ_CP009280.1\|WP_042138951.1\|5857830_5858502_+\|SOS-response-associated-peptidase	gnl\|CDD\|376837	pfam02586, SRAP, SOS response associated peptidase (SRAP). The SRAP family functions as a DNA-associated autoproteolytic switch that recruits diverse repair enzymes onto DNA damage. We propose that the human protein Q96FZ2:UniProtKB, the eukaryotic member of the SRAP family, which has been recently shown to bind specifically to DNA with 5-hydroxymethylcytosine, 5-formylcytosine and 5-carboxycytosine, is a sensor for these oxidized bases generated by the TET (tetrahedral aminopeptidase of the M42 family) enzymes from methylcytosine. Hence, its autoproteolytic activity might help it act as a switch that recruits DNA repair enzymes to remove these oxidized methylcytosine species as part of the DNA demethylation pathway downstream of the TET enzymes.	8.77819e-118
NZ_CP009280.1\|WP_081970086.1\|5873789_5875091_-\|DUF4432-family-protein	gnl\|CDD\|379620	pfam14486, DUF4432, Domain of unknown function (DUF4432).	8.08868e-10
NZ_CP009280.1\|WP_042138963.1\|5875080_5875821_-\|beta-phosphoglucomutase	gnl\|CDD\|213672	TIGR01990, bPGM, beta-phosphoglucomutase. This model represents the beta-phosphoglucomutase enzyme which catalyzes the interconverison of beta-D-glucose-1-phosphate and beta-D-glucose-6-phosphate. The 6-phosphate is capable of non-enzymatic anomerization (alpha <-> beta) while the 1-phosphate is not. A separate enzyme is responsible for the isomerization of the alpha anomers. Beta-D-glucose-1-phosphate results from the phosphorylysis of maltose (2.4.1.8), trehalose (2.4.1.64) or trehalose-6-phosphate (2.4.1.216). Alternatively, these reactions can be run in the synthetic direction to create the disaccharides. All sequenced genomes which contain a member of this family also appear to contain at least one putative maltose or trehalose phosphorylase. Three species, Lactococcus, Enterococcus and Neisseria appear to contain a pair of paralogous beta-PGM's. Beta-phosphoglucomutase is a member of the haloacid dehalogenase superfamily of hydrolase enzymes. These enzymes are characterized by a series of three catalytic motifs positioned within an alpha-beta (Rossman) fold. beta-PGM contains an inserted alpha helical domain in between the first and second conserved motifs and thus is a member of subfamily IA of the superfamily. The third catalytic motif comes in three variants, the third of which, containing a conserved DD or ED, is the only one found here as well as in several other related enzymes (TIGR01509). The enzyme from L. lactis has been extensively characterized including a remarkable crystal structure which traps the pentacoordinate transition state. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	3.80648e-88
NZ_CP009280.1\|WP_042138960.1\|5866410_5866623_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	1.8912e-18
NZ_CP009280.1\|WP_081970087.1\|5881716_5883549_+\|sensor-histidine-kinase	gnl\|CDD\|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	5.83462e-51
NZ_CP009280.1\|WP_042138965.1\|5883541_5885164_+\|response-regulator	gnl\|CDD\|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.29053e-47
NZ_CP009280.1\|WP_042141443.1\|5880051_5881359_-\|extracellular-solute-binding-protein	gnl\|CDD\|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.79406e-45
NZ_CP009280.1\|WP_156118685.1\|5885189_5886089_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|378940	pfam12746, GNAT_acetyltran, GNAT acetyltransferase. Many of the members are annotated s being Zwittermicin A resistance proteins, whereas others are listed as being GNAT acetyltransferases. The family has similarities to the GNAT acetyltransferase family.	1.96417e-19
NZ_CP009280.1\|WP_042138964.1\|5878924_5879800_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.60254e-55
NZ_CP009280.1\|WP_039308352.1\|5878079_5878904_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	9.89217e-79
NZ_CP009280.1\|WP_042138959.1\|5865552_5866329_-\|NAD(P)-dependent-oxidoreductase	gnl\|CDD\|223528	COG0451, WcaG, Nucleoside-diphosphate-sugar epimerases [Cell envelope biogenesis, outer membrane / Carbohydrate transport and metabolism].	3.04991e-24

>NZ_CP009280.1|WP_042138961.1|5866750_5866945_-|hypothetical-protein
MEKELILEKSRQEKNDEGREFVHNRGRKFGVLGMLIIFSILAVYNLYDNHQETNTALVAVFMGI
>NZ_CP009280.1|WP_042138960.1|5866410_5866623_-|helix-turn-helix-transcriptional-regulator
MNDKLILRNRLREARAEQKISQAELAEMVGVSRNTISSIETGQFNPTAKLALVLCIALDMKFEELFYFDL
>NZ_CP009280.1|WP_042138959.1|5865552_5866329_-|NAD(P)-dependent-oxidoreductase
MKRKLLLTGAAGRIGNALFKGLNEDGRYEVTGADIQADEEQGIAQLDINDEARLAELTKDVDTVLHFAWIKDEDDFLGKVLQGNVAGAYKLFEAAVQNGVRRIIFASSNHATGYYKSDETTGPSDPYRPDSFYGLSKCYIELLGRLYSDQGKISSLNIRIGNFPGDDRPHSERAGHIWISERDLLQLVNCCIQADEDLQYLNLYGTSANSDNYYTIGYLEELIGYKPQDDAAELLEQAKAEGWEIRKDETEYQGGQQE
>NZ_CP009280.1|WP_042138958.1|5864471_5865173_-|hypothetical-protein
MLFGIQTSVLIVAVFTAFVGYQFRLREKKRDMAHSELIKSYNDFYSPILFVIREINELPQSEERNDLINKLFTDYGLGSSKGHLIGSVNMLNTYFELNALFRAFKHQPDAYEAKFLKCLKEFEVMIDQEFWDAHDIIYKEHNRYKDHNFKPLKSLFIDLLGTLKFVSDFAMSVCLLTWFTIGYAHIFNIEAFSVKAVGYITGFTVIVILIFVGSFMYSKLFYSKTNNRRERKK
>NZ_CP009280.1|WP_156118684.1|5863665_5864070_-|hypothetical-protein
MSRANVEKVLGEAENDGSRGMMFYNNGVGVLYRENSAVAILMNEDSKGSFITSGGLEVNMNKNDLYKIYDKKNAIEASGSLTFAYDSFNKKYLKEVKYDSDQTNQSYLISVEFNDKGEAERIVVSDIQAALLAN
>NZ_CP009280.1|WP_042138956.1|5863365_5863641_+|hypothetical-protein
MDRKLKQSLKVAAVRRELIVVWLLNGDKIKGIAEVSADPERVKINIIEGPVWVLYIDVEISLVISLRLRVKRKNEPSHPATSFLFIKLAIK
>NZ_CP009280.1|WP_042138955.1|5861738_5862056_-|hypothetical-protein
MKGITVLLVLITVLITAGCSDTYEKSDTDAAGRDLMLAETTQYLFNYEHNSKDTSSESAEFINECLDIYSGDDLEDYKLLVSYIEMDDIEHVKELQRKLGGDIIE
>NZ_CP009280.1|WP_052421987.1|5858554_5859595_-|fibronectin-type-III-domain-containing-protein
MKQWKSIASKLILVIFTGILFFTVQTSTYAAAVGDQLTSPEAGWKRYDDTHAGLKYTGSWYTATGTSYYNGSAKVTTKAADNNYVSFSFYGTELRLIADRNTDRHSDNTITIDGVTETFTEYSTTSTKQVLVYEKTGLPLGAHTVNVTVGHNRINFIVDAIDIDDTGYLINTNLSSPLDLSAAAAIEKIDLSWTAVTNATSYNVKRSTTTGGLYETIASNVTNATYTDINVTSDVKYYYVVTAVNAAGESISSNETSAIPLAATVPDNGRAILTIYLNNGTEKEYDLSMTEVNAFIDWYDQKDAGVGTAKYAFIKAWNKGPFIKRTEYVVFDKILTFNVDEYAAEE
>NZ_CP009280.1|WP_042138951.1|5857830_5858502_+|SOS-response-associated-peptidase
MCGRFTITVTLEELIAHYLIDDSKIATLKPNYNVAPMHNVPAVIASDAGKRLGELRWGLVPFWAKDEKIGSKMINARAETVADKPAFKRLLKTKRCIIPADGFYEWKKDGTSKQPYRILMSDGSLFSFAGLYDTWEDPEGKKLSTCTIITTTPNSLMEDIHDRMPVILRPEDEADWLGRDNDDVESLLKLLKPYDAAKMRAYKVPSAVGNVRNNSKELLEDIG
>NZ_CP009280.1|WP_042141433.1|5857044_5857728_+|pectate-lyase
MLLKKVVGLLLSVVMLSSFYVASPAKVSAATPIVVSTTIVVPAGETFNGNGQTYVANASTLGDGSQAENQKPIFRLEKNATLKNVIIGAPGADGVHCYGNATISNVTWQDVGEDALTLKASGTVNITGGGAYKAYDKVFQANAAGTINIKNFRADDIGKLARQNGGTSYAVNFTLDSSDISNAKDSIFRTDSSSSAAKITNTRYHNVPTLFKGFASGKTSQSGNTQY
>NZ_CP009280.1|WP_081970086.1|5873789_5875091_-|DUF4432-family-protein
MRNEWKSDERICNERVSDERISDELISKGRVSNKRISDETNSNEQKNYQRISNEPNSDEQNSNQRISELTLEQLQPGTPQVLPGGGFVTLTLVTDSFGSHLHLLTISNGRLVFTVILERGMDIGEIRLDAEKISWEREERYLLHPDHVDLSDNEHSGWDSGFYAAVAAIGPEIFGTPDEVRTVHGTGSYSPALPESVRLTWDEQQICLEGNVPVRGYGPLPVYAKTVRIVTRYGAANLFREDTVRNLTEVAQPVDDGYHIQLAGAYMSGGGSYILPVSTAKMLLRDSAPPEVDPLAVYDSETRLDPIRCYQYVPEPVEGLADLPQVRDYCADGGGEQLTAEMLVNAGQDTAAYVIRSLQCYPRSLIAKRAVTDRMYALEPCKTRPNSLEQKTIDGEVVYIGPRGQSIGWIIIGASRDPKEITTLAHMIRSAAK
>NZ_CP009280.1|WP_042138963.1|5875080_5875821_-|beta-phosphoglucomutase
MKCTSWKGGAMLRAQPFEAAIFDLDGVIVDTAKFHYQAWKRLAGELGFDFSESSNEQLKGVSRMESLELLLRSGGITDLTAERKEELASRKNEWYKELLDTLTPGDVLPGVSGFLGLLRSRGVRTAIASASKNAPLILEKVNIRPLFDAVADGNTIGRAKPDPEVFLQAARLLGVAPAACFVFEDADAGVEGAIRAGMRVVGVGDGALLARADLTIASFEQLDPVFLLSHIGLNGDSGKGDCSNEE
>NZ_CP009280.1|WP_042141438.1|5875768_5878060_-|glycoside-hydrolase-family-65-protein
MERYRRIEGLQMNEEHLWCLKENGYEAGLHKHYEGLFTQGNGYMHARGSFEEGCSDAPQDEEYLRFPDNVTLEKPRHPKSKQGTFIPGIVARHPLLKEEIVNLPYMLGLELRSAGESLDMDRSRISGYRRWLDLRDGSLHRTLIWETAEGMQLQCTFERYISMADTHLCIQRIQVEVLAGEGRLEAAASLRGDVRTNGMNHFDSVVPTAEVGGSLSLETLTEQGNRIFMHSALEASEAVIWQEENSQVTAALRGEFAVQTGDRLTVSKLTAVTTDRDMEEGEAGSRALAQLSRAREIGWDQLYERHAACWKSKWQGADILIKGDDLAQLNVRASLYHLLRANAPEDARVAICAKGYAGEAYFGRYFWDTEINLLPFYLHTNPQAARNLLLFRYNTLDGARRNAQSYGYRGARYAWESSLSGDEQCANWQYADHEIHITADIVYALYHYVRATGDQDFLEHYGIDILVETARYWCDRVDWNREEVGELLGVMGPDEYLPFTRNNAFTNRMVKFSLEQTVTCLDSLQGSKPDSYAAAVERLGIRPEEQELFRHTAEKLRLPYDSGTEIVPQSDDFASYADVDFARIWTDRSRPFGHFISQERNYRSKALKQADVLELMLLFPQEFSKEQLKASYDYYEPITTHDSSLSVAVHGIVASWLNQPEAAANFLKRVMAIDLSLEKKGAAEGIHIANCGGLWQLIVYGLAGLKSAMWSKDIELAPRLPEGWTELSFQLAWQGERYRITIHPDAHEVHKLEGRGYVAGTTL
>NZ_CP009280.1|WP_039308352.1|5878079_5878904_-|carbohydrate-ABC-transporter-permease
MLKKSLGVLKYGFVILIVLLSLGPFLWVLLASFKTNAEILSNSLGWPSSFRFSNYTKAFQIAPISRFYINSVIVGIFGTLLNLLLLGMAAYVLARFQFRGKKLLMGAFSLSLLIPGAAMLQPLYLTVNALGLYDKLIGLIIVYTGFGLPVSLYILSSYFLTIPKEMEESAYLDGASFIQTFFRIILPISKPGFGTAGVMQFLLCWNEFQFAIILTTGNQSRTLPLALYYFKSQFASDYGVMFAATMVVIIPSIVVYILLQEQVVSGLAAGAVKG
>NZ_CP009280.1|WP_042138964.1|5878924_5879800_-|sugar-ABC-transporter-permease
MVRKNRGYITLFLLPTVALFIIVYAVSLVILFGTSFTEWSAGRSPVFIGLANYIRLFTDDADFRQSALNTGIWVVLQSTVHVAIGTLFAVILSMKEFYWKFARTVYMFPNIISGAAVGMLFLCMLNPEFGAVNSIVRLFGNADYSQNWFMDYATAFLSVTMTWLPYAAVVTILILAEIAAIPESLFESARIDGASNFKINLYIIIPMLRNIIGTCVILSGTSMLQKMDIILMTTGGGPGNQTMNLPIYIYKTALMDNNFGYSNSVGVFLIGFGLIFVLLCRNLFRIGSSQN
>NZ_CP009280.1|WP_042141443.1|5880051_5881359_-|extracellular-solute-binding-protein
MLMLTMSITACGSGNSAENNGAAATAGSGNAAAPAAKAPVKISYLTFRVGTHASAKMEEEQIKQFNAKYGNEVEVVVEEIPSDAAYVDKIKILAASGDVPDVVMGKDGINDVLIKGNLATPFNDYLDKDAEWKAAIGEDALASNTRDGKIWSISDQKQNIGYFYNKEMFEKAGIKPAETWDEFMSNNEKLKAAGFVPLALMTGENAWTSNLILAAMIGTNGENGKTFMNTLHPTDFNTPEMIQALNMMKELLEKYTTKDALGAGYANAANAFSQGKAAMIANGPWMIGDFSDPTKSSEGFDAKVGVAAYPNNSLISTYEVGYMIGAKTPETRDAAEKFIKFKTGLEGQTLALEYGNVMPVSSEVQPSDALKEKYPIMVESITVAQKSQLHYRTLDSIVYPNVTDAWKNLYPKLAAGRATAEEIAKELTEIAAKNK
>NZ_CP009280.1|WP_081970087.1|5881716_5883549_+|sensor-histidine-kinase
MSNQHILKRISLRPLLGRFSLIPVRNKMVIIIFLLILLPMTFAGCYFYWSISQILTRNANDNLSLLIRQTNDNIEKSFQIIDNTSLHFLSTKMLRNWLIDDMSLSDDFYKKFVNKSEMEEDLKYSLMFNNAWNISLLSTAYVFFDNDNYVSVLKSPPNIEQINRNNLAVYQSVNGRMVRGKEILTPSPGDPTLYFTRVMSNINLPEQRLVLIFGTNEADLAEEYAGLLEYPGAIAYIIDNQGVIYSSAGKQELGSTVPPDVLALRDHTEVSEVKLNQETYLAASRSIGTTGLTFIAGIPRKQVLAKLSGSMHNYIWFIALIAFVSLAAGVLLSLRFTRIIRDLLRSIRKVKKGDYNTRMPAFKDAELNQLSSTFNNMTDEINYLIKEVYEKHLLVKESEFKFLQAQMNPHFLFNTLITIGYKAKLSKDETVYKMVTSLTELLQASIYSNSLAKIPIRQELDFIRFYLYLQKERFEDKMEYTIQIEDEAILDLLLPKLSVEPLVENAVVHGVERKLGKGNINIRIYRKNDSVYFEITDNGSGFEHVPKNWGHFESDTMRKQGHNNIGLINTHKRVKLLYGEPYGIEVESEPGTGARVTLHIPADQGELTHV
>NZ_CP009280.1|WP_042138965.1|5883541_5885164_+|response-regulator
MYKVMIVDDEPVIKKGLQCFIDWSILECEVVCEASNGLEAVELLGYYDVDIVVTDIRMPGMDGLALSDYLHQHFPQTKVIILTAFADFSYAQTAIQYEVVDFVVKTNPTEQIPRAIEKATLLLEKEREQKQKVRQLESKINDNLSEISEKFLREAVYGLISDEAGLYSRSSELGLQLEDYFAIYMEVKDIPGPHGSAGSPANDHYRFLASIRHFLALAFGEHPSYIMAMEKNTLLALVSMTGGNTAVSTQALLTISNEILAMAENFRQYHVNIGISLRHRDISTLSTAYLEAREALQGSFYNDNYVAVYIPHANQALTPAAPPHHAAEQIAGHLQQGDSESAIRQLDQLLENYRSIKEPIENVKVACLLISSYCFRLLSTSQPFAPEMEESQSAVYKQIQESKSIQLLADILGRLILSCSRAVARSDRQPNYIVIECQKYIREHYNQNLSLQIIADHIHINSSYLSRLYKKVTGESIIDVINKYRIDMAKKLLRNPASKVFEVAEAVGIETPAYFTHVFSKYTGMSPKEYKLNYSQTELG
>NZ_CP009280.1|WP_156118685.1|5885189_5886089_-|GNAT-family-N-acetyltransferase
MIESSETTLLAGRADNDAFNQALTESLGFWEQVTPDNEEWRLKIPEVHPNKYIREYTRHRYIVTRETFTPIELSLPEGYVPEKIDLPELRKKSYKNADKIYKWAAEWGSDEHFAIAGCGCYIRHLDKIVSWSLSDCYNGGQVAIGIQTARSYRKMGLAKQVVSAVVQQCWDKGYGSVEWLCVSTNRGSRAVAERVGFMLADTYPSFTSYAPIENFADLNDDGWYEWGAYLQQASQKEPRLYLECLHCYVKANAVEKAQKIVQEMTKAEIECDLEELNGAIAYYRSEGLCSAFKAPEWTI
>NZ_CP009280.1|WP_156118686.1|5886072_5886228_-|hypothetical-protein
MIELKNEQYGKAKELVTSHNELSVFTVLEGLMGQGSCGFGRTSASPDDRVQ

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_CP009280_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_18

7027241-7027371

Orphan

Consensus_repeat	Method
ACAAATAATCCGGAGCAGACTGGAGATTTGAGAACAGGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_18

>merge|NZ_CP009280|18|7027241-7027371|CRISPRCasFinder
ACAAATAATCCGGAGCAGACTGGAGATTTGAGAACAGGAAAGTGCGTCGCGGAAATTGCGGGATGAACGAGTTGTGGGACGAACGATCAAGAACAAATAATCCGGAGCAGACTGGAGATTAGAGAACAGGA

>NZ_CP009280|18|16|7027241-7027371|CRISPRCasFinder
ACAAATAATCCGGAGCAGACTGGAGATTTGAGAACAGGA	AAGTGCGTCGCGGAAATTGCGGGATGAACGAGTTGTGGGACGAACGATCAAGA
ACAAATAATCCGGAGCAGACTGGAGATTAGAGAACAGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_081970236.1\|7037176_7038007_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133055
NZ_CP009280.1\|WP_052422078.1\|7027788_7029615_+\|FTR1-family-iron-permease	unknown	unknown	gnl\|CDD\|223744
NZ_CP009280.1\|WP_042139739.1\|7025756_7027106_+\|deferrochelatase/peroxidase-EfeB	unknown	unknown	gnl\|CDD\|273606
NZ_CP009280.1\|WP_042139738.1\|7024825_7025752_+\|iron-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|225378
NZ_CP009280.1\|WP_042139741.1\|7032439_7033645_+\|N-acetylglucosamine-6-phosphate-deacetylase	unknown	unknown	gnl\|CDD\|238434
NZ_CP009280.1\|WP_042139731.1\|7017245_7018172_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_CP009280.1\|WP_042139733.1\|7019479_7020469_-\|ATPase	unknown	unknown	gnl\|CDD\|225518
NZ_CP009280.1\|WP_019908812.1\|7022439_7022664_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP009280.1\|WP_042139732.1\|7018196_7019495_-\|6-phospho-beta-glucosidase	unknown	unknown	gnl\|CDD\|133432
NZ_CP009280.1\|WP_042139734.1\|7020489_7021479_-\|LacI-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_CP009280.1\|WP_042139744.1\|7034985_7036074_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP009280.1\|WP_042139748.1\|7037924_7038500_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP009280.1\|WP_042139736.1\|7023142_7024120_+\|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380509
NZ_CP009280.1\|WP_042139746.1\|7036136_7037180_-\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP009280.1\|WP_042141602.1\|7038614_7039331_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133055
NZ_CP009280.1\|WP_042141601.1\|7031723_7032452_+\|glucosamine-6-phosphate-deaminase	unknown	unknown	gnl\|CDD\|238693
NZ_CP009280.1\|WP_042139735.1\|7021796_7022072_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042139740.1\|7030845_7031724_+\|MurR/RpiR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224651
NZ_CP009280.1\|WP_042139742.1\|7033857_7034868_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131944
NZ_CP009280.1\|WP_042139730.1\|7016258_7017149_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_081970236.1\|7037176_7038007_-\|glycosyltransferase	gnl\|CDD\|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.72247e-31
NZ_CP009280.1\|WP_052422078.1\|7027788_7029615_+\|FTR1-family-iron-permease	gnl\|CDD\|223744	COG0672, FTR1, High-affinity Fe2+/Pb2+ permease [Inorganic ion transport and metabolism].	6.40746e-38
NZ_CP009280.1\|WP_042139739.1\|7025756_7027106_+\|deferrochelatase/peroxidase-EfeB	gnl\|CDD\|273606	TIGR01412, Probable_deferrochelatase/peroxidase_EfeN, Tat-translocated enzyme. This model represents a small family of proteins with a typical Tat (twin-arginine translocation) signal sequence, suggesting that the family is exported in a folded state, perhaps with a bound redox cofactor. Members of this family show homology to Dyp, a dye-decolorizing peroxidase from Geotrichum candidum that lacks any typical heme-binding site.	5.98111e-158
NZ_CP009280.1\|WP_042139738.1\|7024825_7025752_+\|iron-ABC-transporter-substrate-binding-protein	gnl\|CDD\|225378	COG2822, COG2822, Predicted periplasmic lipoprotein involved in iron transport [Inorganic ion transport and metabolism].	1.91479e-99
NZ_CP009280.1\|WP_042139741.1\|7032439_7033645_+\|N-acetylglucosamine-6-phosphate-deacetylase	gnl\|CDD\|238434	cd00854, NagA, N-acetylglucosamine-6-phosphate deacetylase, NagA, catalyzes the hydrolysis of the N-acetyl group of N-acetyl-glucosamine-6-phosphate (GlcNAc-6-P) to glucosamine 6-phosphate and acetate. This is the first committed step in the biosynthetic pathway to amino-sugar-nucleotides, which is needed for cell wall peptidoglycan and teichoic acid biosynthesis. Deacetylation of N-acetylglucosamine is also important in lipopolysaccharide synthesis and cell wall recycling.	3.33066e-142
NZ_CP009280.1\|WP_042139731.1\|7017245_7018172_-\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.06056e-117
NZ_CP009280.1\|WP_042139733.1\|7019479_7020469_-\|ATPase	gnl\|CDD\|225518	COG2971, COG2971, Predicted N-acetylglucosamine kinase [Carbohydrate transport and metabolism].	1.10757e-36
NZ_CP009280.1\|WP_019908812.1\|7022439_7022664_-\|response-regulator-transcription-factor	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.10543e-19
NZ_CP009280.1\|WP_042139732.1\|7018196_7019495_-\|6-phospho-beta-glucosidase	gnl\|CDD\|133432	cd05296, GH4_P_beta_glucosidase, Glycoside Hydrolases Family 4; Phospho-beta-glucosidase. Some bacteria simultaneously translocate and phosphorylate disaccharides via the phosphoenolpyruvate-dependent phosphotransferase system (PEP-PTS). After translocation, these phospho-disaccharides may be hydrolyzed by the GH4 glycoside hydrolases such as the phospho-beta-glucosidases. Other organisms (such as archaea and Thermotoga maritima ) lack the PEP-PTS system, but have several enzymes normally associated with the PEP-PTS operon. The 6-phospho-beta-glucosidase from Thermotoga maritima hydrolylzes cellobiose 6-phosphate (6P) into glucose-6P and glucose, in an NAD+ and Mn2+ dependent fashion. The Escherichia coli 6-phospho-beta-glucosidase (also called celF) hydrolyzes a variety of phospho-beta-glucosides including cellobiose-6P, salicin-6P, arbutin-6P, and gentobiose-6P. Phospho-beta-glucosidases are part of the NAD(P)-binding Rossmann fold superfamily, which includes a wide variety of protein families including the NAD(P)-binding domains of alcohol dehydrogenases, tyrosine-dependent oxidoreductases, glyceraldehyde-3-phosphate dehydrogenases, formate/glycerate dehydrogenases, siroheme synthases, 6-phosphogluconate dehydrogenases, aminoacid dehydrogenases, repressor rex, and NAD-binding potassium channel domains, among others.	0
NZ_CP009280.1\|WP_042139734.1\|7020489_7021479_-\|LacI-family-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	6.2342e-118
NZ_CP009280.1\|WP_042139744.1\|7034985_7036074_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	4.81647e-30
NZ_CP009280.1\|WP_042139748.1\|7037924_7038500_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	5.03207e-09
NZ_CP009280.1\|WP_042139736.1\|7023142_7024120_+\|LacI-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|380509	cd06286, PBP1_CcpB-like, ligand-binding domain of a novel transcription factor implicated in catabolite repression in Bacillus and Clostridium species. This group includes the ligand-binding domain of a novel transcription factor implicated in catabolite repression in Bacillus and Clostridium species. Catabolite control protein B (CcpB) is 30% identical in sequence to CcpA which functions as the major transcriptional regulator of carbon catabolite repression/regulation (CCR), a process in which enzymes necessary for the metabolism of alternative sugars are inhibited in the presence of glucose. Like CcpA, the DNA-binding protein CcpB exerts its catabolite-repressing effect by a mechanism dependent on the presence of HPr(Ser-P), the small phosphocarrier proteins of the phosphoenolpyruvate-sugar phosphotransferase system, but with a less significant degree.	7.227e-110
NZ_CP009280.1\|WP_042139746.1\|7036136_7037180_-\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.15611e-26
NZ_CP009280.1\|WP_042141602.1\|7038614_7039331_-\|glycosyltransferase	gnl\|CDD\|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	3.52062e-35
NZ_CP009280.1\|WP_042141601.1\|7031723_7032452_+\|glucosamine-6-phosphate-deaminase	gnl\|CDD\|238693	cd01399, GlcN6P_deaminase, GlcN6P_deaminase: Glucosamine-6-phosphate (GlcN6P) deaminase subfamily; GlcN6P deaminase catalyzes the reversible conversion of GlcN6P to D-fructose-6-phosphate (Fru6P) and ammonium. The reaction is an aldo-keto isomerization coupled with an amination or deamination. It is the last step of the metabolic pathway of N-acetyl-D-glucosamine-6-phosphate (GlcNAc6P). GlcN6P deaminase is a hexameric enzyme that is allosterically activated by GlcNAc6P.	3.86067e-135
NZ_CP009280.1\|WP_042139740.1\|7030845_7031724_+\|MurR/RpiR-family-transcriptional-regulator	gnl\|CDD\|224651	COG1737, RpiR, Transcriptional regulators [Transcription].	9.17072e-74
NZ_CP009280.1\|WP_042139742.1\|7033857_7034868_-\|hypothetical-protein	gnl\|CDD\|131944	TIGR02898, Uncharacterized_lipoprotein_YlaJ, sporulation lipoprotein, YhcN/YlaJ family. YhcN and YlaJ are predicted lipoproteins that have been detected as spore proteins but not vegetative proteins in Bacillus subtilis. Both appear to be expressed under control of the RNA polymerase sigma-G factor. The YlaJ-like members of this family have a low-complexity, strongly acidic 40-residue C-terminal domain that is not included in the seed alignment for this model. A portion of the low-complexity region between the lipoprotein signal sequence and the main conserved region of the protein family was also excised from the seed alignment. [Cellular processes, Sporulation and germination].	1.86296e-17
NZ_CP009280.1\|WP_042139730.1\|7016258_7017149_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.43221e-56

>NZ_CP009280.1|WP_042139739.1|7025756_7027106_+|deferrochelatase/peroxidase-EfeB
MKKKDRTSRETPATESVLSKDASKDQLLFDKKLSRRDMLRLTGASGLGLLLGGGGVGSILAARKAAGQPGQALSSPQHAGADIIPFYGNHQAGIITPAQNFLCFASFDLTTTKLSEVKKLLEAWTTAAAALTAGTLIGSVNDNPNLPPADTGEADGLTPSKCTLTFGAGPAFFDSRFGLAAKRPASFTDLPAFTGDSLEPQWCGGDLCVQACADDLQVAFHAIRNLARIARGTAVLRWTQEGFQRTGSADPAGGTPRNLLGFKDGTGNPDVTDDAEMRSVVWSGSGDGPAWMNGGTYLALRRVRFRIEVWDRSTLSDQEATFGRHRQSGAPIGARDEFAELNLEAADASGKPVIPPDSHSALAHGDGSVKMLRRSYSYSSGMDLKTGQLDAGLVFISFQKDLVKQFVSIQQRLSKNDRLNEYMVHTGSAVFACFPGVREGGYIGETLLG
>NZ_CP009280.1|WP_042139738.1|7024825_7025752_+|iron-ABC-transporter-substrate-binding-protein
MKIGYAVPAGLLAASLLFAGCASNDNNNNGNNGNNSNTSGNNAAAQTGNVSTGTPAATADSTAAGVTADFTTAIDEYRKYVIEQCDEFVKQTEGFTNAVKAGKLEDAKALYAPARMYYERIEPIAEALGDLDPNIDARENDVDAADWRGFHKIEQALWQNNTTDGMTDVADRLLKDAQLLRAKVETAEIDANLLVTGAVELLNEVSSSKVTGEEERYSHTDLYDFVANVEGAQKIYELLKPELAKKDPELEQTIGERFTALLNELAPFKSGDGYVSYETLKEAEVRTLSQNLDALAEPLSNMGTILGV
>NZ_CP009280.1|WP_042139736.1|7023142_7024120_+|LacI-family-DNA-binding-transcriptional-regulator
MANIKEIARIAGVSVTTVSRVLNNHPYVSKDKRAAVLDTIEQLNYTRNMNAVHLITGRTGTVAVILPYINAFYFSIIMNGLAHEALLAQYRLILCQSNYLADEEIKVLEMLRNKEIDGVVIVSTALKPELIEEYTAYGPVVTCQDSGQRRYSSVYIEHYAAFKQGLQYLKGKGYRTIGYCEGRQNGSSASIRQTAFREFIAEHKLVFQEEWMIYDCTTEEDGAAVARSLLEMPKRPEAMIITGDHVAAGLMIEARKAGLSIPGDLAVMGFDNQPIGRLLEITTIDNHLYEMGASAFRIIHEQISSDNPDPVYRKLDYRIIERSTV
>NZ_CP009280.1|WP_019908812.1|7022439_7022664_-|response-regulator-transcription-factor
MKGNEHHSKFLLTHREREVFELLVQDKTTRDIAGLLFISEKTVRNHISNVMQKLNVKGRSQAVVELIKLGELKI
>NZ_CP009280.1|WP_042139735.1|7021796_7022072_+|hypothetical-protein
MKWGEITKLHPSRFVLVEAIKASFSNRVRQLEDMAVIQDYDKSEEAWTGYKEMHKLHPTRELYVFHTSRSDVEVVEEFFSGVRQPLLTPMH
>NZ_CP009280.1|WP_042139734.1|7020489_7021479_-|LacI-family-transcriptional-regulator
MNIHDVAKKSGLSVVTVSRVLNNSPSVREGNRQKVLSAIEELNYQPNSAARSLVRGKTGVIGMSITNFNDSFYDRVIRVVNRKLAEQGYFLALSIAENEDDGVNFLFQKDRVDGIILLSPLEEKEYVEELKRKNIPVVLLDNQFQHEDVPSVLVDNYQGGYEATKHLIGLGHTRIAYIGGPSVFLSVTERKRGYVQALDEAGLTPFGTEYCGFTVSSGYEVAKRWIREDKLPTAIFSGDDFIALGVVQALREEGILVPQDISVVGFDDQQFVGEFYPRLTTVRQPEAQMGNIGVELLLKLINGEVTQPAVTKLAPQLLIRESTASVRLT
>NZ_CP009280.1|WP_042139733.1|7019479_7020469_-|ATPase
MKYFLGVDAGGSKTCAMIADEQGKVIGAGKSGNGNHQLGREQAADSLHQAVSEAITASGLTRDQLDYSWFGLAGADREADFRILRPIIGSLGLPRTEISCDTWNALRSGTEKNYGIVLICGSGVNCSGKNPSGATYQCGGFGYRFGDFGGGYDLSMEVFRSVLRADDGREMETVLSKGLTQLLGYTTVSELREDYLDHFRDLPPQIAELLFQAAEEGDPVATGLLVKQGDELGLAAASAIRRLAMEEDIFDIVLAGSLLTKGDRSGIIRRAIERRVKLAAPNGTLRILTREPVVGSVILAMESSGVHVNQEVLDHLSEGKEGQLSWRKH
>NZ_CP009280.1|WP_042139732.1|7018196_7019495_-|6-phospho-beta-glucosidase
MEETLKLVVIGAGSSYTPELIEGIILHHQELPIREIWLVDIEEGREKLHTIAELSKRMIAESGLPITVVETLERREAIAGADFVCTQIRVGMLEARKWDERIPLQYSVIGQETTGPGGMMKGLRTIPVILDICRDIEELAPDAWLLNFTNPAGMVTEAVHKYSSVKSVGLCNSPIGFQKWLSGFFGLPMEKIYAEFVGINHLHWVSDVVIDGKSKLQELIDYPESYKAGNVPFDAWDHRFLNSLQAIPSYYLSYYYMTDEMLAEQKEAAATTGSRAEVVKKVEEELFELYRNIELKEKPKQLEQRGGAYYSEAAVLLMRSIHNDSRDIQTLNVRNNGIIDFLPDDASIEVNCVVTKQGPLPIPLRRVPQSVRGLLAAVKQYESLTIEAAVHGDRGVALQAMVHHPLMPSVTVAEQLLDEMLEKNKPYLPLFH
>NZ_CP009280.1|WP_042139731.1|7017245_7018172_-|sugar-ABC-transporter-permease
MNTAGKASRWKRFTSQLDLQSMVWPGIIFVFIFSYIPMYGVVMAFQQYDIFSGMMKSPWVGLMQFRMFFEAPEFWNVMRNTIVISLLKLIISFPAPILLALMLNEVGHMGFKRVIQTVSYLPYFLSWVIVSGFVFSLLSVDNGTVNYVLERFNLAGEPINFLAVPKYFWSILVSVNVWKEVGFGSIVYLAAIAGIDPTLYEAASIDGASRFKQIHLITLPSITPIIVIFMILAIGSLLSAGFEDILLLATNPILRPYSDVIDTYVYRVGILNARFSYATAVGLFKAVISIILLVTANTIARRANVSLW
>NZ_CP009280.1|WP_042139730.1|7016258_7017149_-|carbohydrate-ABC-transporter-permease
MRLSLGDKVMQRTIYILLTLLALLMLYPFWNALVISFNLGSDTALGGVTLLPRAFTLENYYIVFQDDRLLNSFLITILRTLIGTALSVFFTALLAYGMSKKTLLFRKQYMVFFMITMFFSGGLIPSYLLIRSLGMLDTFWVLIIPGIISVWNMIVVRTFFSALPEGLEESAKIDGSSNYGIFFRIVIPVSGPVLATISLFTAVSYWNDWFTGAIYITKDHLLPIQTLLRQVMNSNIMTQIGSSNAIALDHMNRNRTITTKSLTMATMMVATLPIILTYPFLQKYFVKGVMIGSLKE
>NZ_CP009280.1|WP_052422078.1|7027788_7029615_+|FTR1-family-iron-permease
MIPMIITVKISPWRQIRAALLLICLLLLLPGAPASASGAPLDELLPPVGSALVESGQSRWDAAAADVESFAALWRSANEGTPDPALAGPAAEVDAALAAAAQALAAGGGAPAKAALSTLARSVDAYVTAAAGGGGGDSGAAGRAAAAKLLPAAERTRDAARSADWTAAAEAYRAVVNGWTPAERGIRGDNPAVYGLLETKMSLLRIALQAEPLREEAALAEAEALVALLSGYSEGKAVDTGSAPAEPASIEGLISYLNKAAASAEAGDSPAAAAVMEQFITAWPSAEGAVQIASPKVYANIENESTAVTGYLLSDPPKLAGALEILDNMLAELTPLAGEQTYTAWDAALILLREGLEAILVLAALLAYLRREAEPAARRWVWSGAAVGLAGSIGIAVLLTYTISQAASGGARELIEGIAGLVAVVMMLTIGRWLHGKSSTAAWNKYVDRQMQGALAKGNLWYLFFIAALAILREGAETTIFYAGMAPAIATSQLLLGIGGALAVLVVLGYAIIALSARLPIAAFFRTATVLIYYLVFRFLGESIHALQVAGKIPAHAESSLPSIGWLGLYPTWETFVPQILILAFILWELLRGRQASRRMRTPNRLTK
>NZ_CP009280.1|WP_042139740.1|7030845_7031724_+|MurR/RpiR-family-transcriptional-regulator
MSPILHALQHDKPKLSQMERKLAERILASPGEIVHMGITDLAEECGISPATITRFCKVLHFKGFPDFKVKLAAELAHSDASPQDGGSSYQDIVAGNPLPFIVEAMQANHLASIRDTTSLLDLGRLQSVIDLLCRARRVDLYGMATSSIVAQDFYQKLIRIGVNCTAFADSHMQITSASSLAAGDVAFAVSYSGETPETIDALTCAAASGAATVSLTSYGSSTLATLADIPLFSSSLEQGMRRGDMASRIAQLHIIDILFTGMVSTRFGDFIPKLEQSYLNVQHYRHKRGGQS
>NZ_CP009280.1|WP_042141601.1|7031723_7032452_+|glucosamine-6-phosphate-deaminase
MNILKFQNEEDFAVTGANLIASLVQSNPKAVLGLATGSSPVGVYAKLVEMHRKGIVSFAKVSSYNLDEYVGLPVDHPQSYRSFMNEHLFNHIDIDPARTHVPNGNAPDLDAECLAYDRMLEDNGPVDLQILGIGSNGHIGFNEPDASLSSGTHVVDLLEETLEANARFFDKLEDVPRQAVTMGIGGILKAKQIVLLVRGEEKAEAVKNALEGPITTQCPASLLQSHPNVVVLLDEGAAKWLK
>NZ_CP009280.1|WP_042139741.1|7032439_7033645_+|N-acetylglucosamine-6-phosphate-deacetylase
MAEINGSTGELLYGKVLTPDGVIQKGVIAVLEGLIQYAGEAAWLPAAYASWQTGTSPEPEGLLIPGFVDVHVHGGAGHDFMYSDAASLDTITRFHASQGTTSMLATTMTAAKADIDRVLSEVNAYRNADGGMPYAQLAGVHLEGPFISPKWPGAQNPGHIVPANTLWLEEWEARYPGMIRQVTLAPEREGALEAIQWLRKHGITAALGHTDATFEEVIAAADAGLNQAVHMFNAMTPLHHRKPGTAGAVLFDPRIRAEVIADGIHVHPAAISIIARLKNGHNLLLITDAMSATGLSDGEYAIGDLPVIVSGGIATLKEHPESLAGSTLTMIRGFRYLVQEIGLSLQEASQAASLTPAVSLGMQRSIGSLEAGKRGDILLLDDELNLRGVWIGGRKLEAEIG
>NZ_CP009280.1|WP_042139742.1|7033857_7034868_-|hypothetical-protein
MLKLVTLQLTILMTGDERMLRSKFGLTVSAALLLGAVSITGCGANNSATDNTVETKSVRGTDGRIYVNSAQNGMRANSFDSMEMSEELANRVAAMPEVRSANVMLVGKSAYVAVMLEEASGGVHAKSTRGIQSYSYGSTSGSGTSGMLSGTGRPAGGLETGIGAGMGGMDNSTRTGRGTAAGNPGMTGTGGSIAGIPGSMTGTGTVGGTGVADPENYLGNGNNGIMSRSNMVDGRHMKRDIDESLGNTIGIRSVSPGNGTAITDKDTLTQDMKDKIAAEVKKGKTDLNNVYVSANPDFVERADYYAQEFRAGHPLKGFANEFRTMVERIFPTRSGY
>NZ_CP009280.1|WP_042139744.1|7034985_7036074_+|glycosyltransferase-family-4-protein
MSGGVILKVLFTFYVPSGGVETLNKLRCESLQKSGIECHVLYLMPGSGSHNQTNFPVFITSVDAEIKAVLDTHNYDAIIVTSDYLLLERLRRLGYGRILIYESQGLGKRSDARNLIIDSVPFLRSYCNAVLIPPTDHLLELFIEICPWLHRYVIPNIVDVQSFQHIPGEPPCDPVIAWVGRLETNKNWSEYLKIAHQIRLHKPDLHLWMFHDPDLAADDQKEQFNRELQSLGLKDRLSVFTNIPNHIMPVYYSSIAGSGGFLLSSSITEGFGYAVAEAICCTCPVLSTDSDGVRSFITHNITGKFYPIGNLEAAVNEGLELMNNIPLREAIRQQGRQHMVSRFGFEQYAHSFREMMNSFSIF
>NZ_CP009280.1|WP_042139746.1|7036136_7037180_-|glycosyltransferase-family-4-protein
MRLTFPILTLSRGGAQRMLAELANRLAEIGHEVVVLLPSHGIVEYEMKCPIITAPATVLTEDDFPYGDVIISNYYTTVPVAERASKQGKGLHIRLALCYEPTFLPNNNLSFASYNITRNLLVLSRWQQEIVRINHGIKGRIVPIGLNPDFTNTHLRGRGGNKIVVSAIMRRPEGGFSGHREQDYLLQQLDIVKQRHPEVEIYIITPPSEYASSETLQAMLGDGRFQIRTPGNDSELSYHYNESDIFVSSSTYDTGSLPGLEAMRCGAALVTVYSGGNLEYCVHGHNCLMSYRYENRLAEDVSALVYNKELRQRLAARGELDSGRFTWERSMQIFQTELFEIVSKQGV
>NZ_CP009280.1|WP_081970236.1|7037176_7038007_-|glycosyltransferase
MRRILHSVKRLARIMRRWMLCWPAKQYKLNREGGERMIPKTKVSVVIPFYNCPYVDLAVKSVLAQSYPDIELIVVDDGSTRYMEKLEAYKDNIVYIRKTNGGTASALNMGIKAASGAYFAWLSADDLFHPDKIKRQMEAIRSSGTSFSHTAYYYINELGERFSGVISMPFHNRGDLIETMMSGCPVNGSSVLLDMEIFNKVGRFNEKFLYTQDYDLWLRILPYYEWSYIEEPLLDYRVHKEMGSVIHSEAQNREIALVQSRHQGILTQLLRKERGK
>NZ_CP009280.1|WP_042139748.1|7037924_7038500_-|class-I-SAM-dependent-methyltransferase
MYREIEVKDFLPVLLEQLKFSESILDIGSGTGTLLERYEAAVVLGLDIHRPYLLHRKYKSPHIIPVHADASHIDKLFLPGTFSAVTLIDSLEHFSMREGTELLRKAEIIASNRVVVFTPRGFFPQEGKDHFNLHGEYYQKHWSGWEPEDFLKLGYAVTVLKGFHHAENPSFREAFGEDHAPLDALLACKTV
>NZ_CP009280.1|WP_042141602.1|7038614_7039331_-|glycosyltransferase
MKPRVSVIIPFYNCPYIEQALQSALAQSWQPYEIIVVDDGSFMHAERITPYLPHIHYLGKANGGTASALNHGIAHSTGDYVVWLSSDDMFYRDKINNQVLFMEQNRLLITYTNFNFINGDSQLTQLNAAAVFHNQLDYLRCFLQGNPINGCTVMFKREIFGAIGLFNEALPYTHDYDLWYRAILNGYPPIMLNQSLTAYRRHDGMGTIKHYDVIMAEAAATNARYHAPLSSLIASMGG

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_CP009280_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_19

7050052-7050128

Orphan

Consensus_repeat	Method
TTCAGGGGCACTTTTGCCACTCTTTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_19

>merge|NZ_CP009280|19|7050052-7050128|CRISPRCasFinder
TTCAGGGGCACTTTTGCCACTCTTTCCTGCCTGCCGCCCACTTTCGGCAGATTCAGGGGCACTTTTGCCACTCATTC

>NZ_CP009280|19|17|7050052-7050128|CRISPRCasFinder
TTCAGGGGCACTTTTGCCACTCTTTC	CTGCCTGCCGCCCACTTTCGGCAGA
TTCAGGGGCACTTTTGCCACTCATTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042141605.1\|7048752_7049532_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226425
NZ_CP009280.1\|WP_042139753.1\|7042188_7043283_-\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl\|CDD\|340819
NZ_CP009280.1\|WP_039307029.1\|7058938_7059151_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235562
NZ_CP009280.1\|WP_081970240.1\|7050436_7050610_-\|aspartyl-phosphate-phosphatase-Spo0E-family-protein	unknown	unknown	gnl\|CDD\|378175
NZ_CP009280.1\|WP_042139758.1\|7047375_7048464_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|226988
NZ_CP009280.1\|WP_052422079.1\|7046209_7047343_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|226988
NZ_CP009280.1\|WP_042141602.1\|7038614_7039331_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133055
NZ_CP009280.1\|WP_042139754.1\|7043369_7043681_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_156118801.1\|7058230_7058752_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP009280.1\|WP_042139750.1\|7040376_7041216_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187564
NZ_CP009280.1\|WP_042141606.1\|7055468_7055978_-\|RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|224511
NZ_CP009280.1\|WP_042139763.1\|7054245_7055469_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042139752.1\|7041212_7042199_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|367154
NZ_CP009280.1\|WP_042139760.1\|7050706_7052140_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042139749.1\|7039330_7040380_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|366597
NZ_CP009280.1\|WP_042139766.1\|7059363_7059654_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_081970238.1\|7044358_7045894_-\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP009280.1\|WP_042139764.1\|7056591_7057929_-\|5'-deoxyadenosine-deaminase	unknown	unknown	gnl\|CDD\|180895
NZ_CP009280.1\|WP_039306867.1\|7059650_7059992_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP009280.1\|WP_042139761.1\|7052156_7054055_-\|LTA-synthase-family-protein	unknown	unknown	gnl\|CDD\|293739

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042141605.1\|7048752_7049532_+\|AAA-family-ATPase	gnl\|CDD\|226425	COG3910, COG3910, Predicted ATPase [General function prediction only].	2.04868e-97
NZ_CP009280.1\|WP_042139753.1\|7042188_7043283_-\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	gnl\|CDD\|340819	cd03786, GTB_UDP-GlcNAc_2-Epimerase, UDP-N-acetylglucosamine 2-epimerase and similar proteins. Bacterial members of the UDP-N-Acetylglucosamine (GlcNAc) 2-Epimerase family (EC 5.1.3.14) are known to catalyze the reversible interconversion of UDP-GlcNAc and UDP-N-acetylmannosamine (UDP-ManNAc). The enzyme serves to produce an activated form of ManNAc residues (UDP-ManNAc) for use in the biosynthesis of a variety of cell surface polysaccharides; The mammalian enzyme is bifunctional, catalyzing both the inversion of stereochemistry at C-2 and the hydrolysis of the UDP-sugar linkage to generate free ManNAc. It also catalyzes the phosphorylation of ManNAc to generate ManNAc 6-phosphate, a precursor to salic acids. In mammals, sialic acids are found at the termini of oligosaccharides in a large variety of cell surface glycoconjugates and are key mediators of cell-cell recognition events. Mutations in human members of this family have been associated with Sialuria, a rare disease caused by the disorders of sialic acid metabolism. This family belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	4.00112e-120
NZ_CP009280.1\|WP_039307029.1\|7058938_7059151_-\|hypothetical-protein	gnl\|CDD\|235562	PRK05687, fliH, flagellar assembly protein FliH.	0.00107035
NZ_CP009280.1\|WP_081970240.1\|7050436_7050610_-\|aspartyl-phosphate-phosphatase-Spo0E-family-protein	gnl\|CDD\|378175	pfam09388, SpoOE-like, Spo0E like sporulation regulatory protein. Spore formation is an extreme response to starvation and can also be a component of disease transmission. Sporulation is controlled by an expanded two-component system where starvation signals result in sensor kinase activation and phosphorylation of the master sporulation response regulator Spo0A. Phosphatases such as Spo0E dephosphorylate Spo0A thereby inhibiting sporulation. This is a family of Spo0E-like phosphatases. The structure of a Bacillus anthracis member of this family has revealed an anti-parallel alpha-helical structure.	1.07452e-06
NZ_CP009280.1\|WP_042139758.1\|7047375_7048464_-\|glycosyltransferase	gnl\|CDD\|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	2.08592e-29
NZ_CP009280.1\|WP_052422079.1\|7046209_7047343_-\|glycosyltransferase	gnl\|CDD\|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	3.68147e-33
NZ_CP009280.1\|WP_042141602.1\|7038614_7039331_-\|glycosyltransferase	gnl\|CDD\|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	3.52062e-35
NZ_CP009280.1\|WP_156118801.1\|7058230_7058752_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.43355e-14
NZ_CP009280.1\|WP_042139750.1\|7040376_7041216_-\|SDR-family-oxidoreductase	gnl\|CDD\|187564	cd05254, dTDP_HR_like_SDR_e, dTDP-6-deoxy-L-lyxo-4-hexulose reductase and related proteins, extended (e) SDRs. dTDP-6-deoxy-L-lyxo-4-hexulose reductase, an extended SDR, synthesizes dTDP-L-rhamnose from alpha-D-glucose-1-phosphate, providing the precursor of L-rhamnose, an essential cell wall component of many pathogenic bacteria. This subgroup has the characteristic active site tetrad and NADP-binding motif. This subgroup also contains human MAT2B, the regulatory subunit of methionine adenosyltransferase (MAT); MAT catalyzes S-adenosylmethionine synthesis. The human gene encoding MAT2B encodes two major splicing variants which are induced in human cell liver cancer and regulate HuR, an mRNA-binding protein which stabilizes the mRNA of several cyclins, to affect cell proliferation. Both MAT2B variants include this extended SDR domain. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	6.9686e-64
NZ_CP009280.1\|WP_042141606.1\|7055468_7055978_-\|RNA-polymerase-sigma-factor	gnl\|CDD\|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	6.89078e-33
NZ_CP009280.1\|WP_042139752.1\|7041212_7042199_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|367154	pfam02719, Polysacc_synt_2, Polysaccharide biosynthesis protein. This is a family of diverse bacterial polysaccharide biosynthesis proteins including the CapD protein, WalL protein, mannosyl-transferase, and several putative epimerases (e.g. WbiI).	4.3196e-123
NZ_CP009280.1\|WP_042139749.1\|7039330_7040380_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|366597	pfam01370, Epimerase, NAD dependent epimerase/dehydratase family. This family of proteins utilize NAD as a cofactor. The proteins in this family use nucleotide-sugar substrates for a variety of chemical reactions.	1.24229e-38
NZ_CP009280.1\|WP_081970238.1\|7044358_7045894_-\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.28682e-29
NZ_CP009280.1\|WP_042139764.1\|7056591_7057929_-\|5'-deoxyadenosine-deaminase	gnl\|CDD\|180895	PRK07228, PRK07228, 5'-deoxyadenosine deaminase.	0
NZ_CP009280.1\|WP_042139761.1\|7052156_7054055_-\|LTA-synthase-family-protein	gnl\|CDD\|293739	cd16015, LTA_synthase, Lipoteichoic acid synthase like. Lipoteichoic acid (LTA) is an important cell wall polymer found in Gram-positive bacteria. It may contain long chains of ribitol or glycerol phosphate. LTA synthase catalyzes the reaction to extend the polymer by the repeated addition of glycerolphosphate (GroP) subunits to the end of the growing chain.	1.29347e-89

>NZ_CP009280.1|WP_042141605.1|7048752_7049532_+|AAA-family-ATPase
MYDPMLYLRHVDLLREQVPSFDTYPFNLPVVRALERIAFQKQVTFLVGENGTGKSTVLEGIAAAWGFNPEGGTLNFSFNTRASHSSLYEYLRIAKGVKRPKDGFFLRAESYYNVATYIDELDEDPEAGRSIKDSYGGNSLHEQSHGESFFSTFVHRFGGQGIYILDEPEAALSPLRQMSLLVRMHELAAQNSQFIIATHSPILMSYPGADIFQLEGERITPVALEDTDHYTVTRAFMTDRQRMLRELLGDDYASDASDI
>NZ_CP009280.1|WP_042139758.1|7047375_7048464_-|glycosyltransferase
MKAKNRNVRPRDYRDGYTEGYRLGLCEAVKRLNSPVVGACRPFKLMYVPQGFQAIDTGVTEALRQLVSELIICSPETMLEVAARESPGAVLVMNGLHVFPENHLEQITEIRKLGIPAAIWFVDDPYFTEDTSVICRHYDYVFTHELGCVEFYRSLGVTSVHYLPLCVNPQMFYPRRTGPQYQYDVVFIGNAFRNRTELFDELAPFLRGKKVLIAGGFWERLNTFEELSPFIKSGFIPPEETANYYSGAKLVINIHRPWEGGQDNRNTFQLPSLSINPRTYEISACGTMQLTDIREDLGSHYRPGHDLETFASADELKRKIDYYLKHEQERRKYALRGLQTTLRHHTFTARLPHLLGVLAAQG
>NZ_CP009280.1|WP_052422079.1|7046209_7047343_-|glycosyltransferase
MNNQFIMPAPPLPRTPAEEQKLSGRLTGFKVGYDEGYLRGRLAILDGRPEEPLPVRNIHVMYVASGKGYPYSPLDDAVLFALQRLTTQVTITDVRQNLVELASAQRPDLVLVLDGLDLPLDQVAVLRGRGIKTAIWLTDDPYYTDFTMKIVAHYDYVFTLERNCVEFYRGLGCSEVHYLPFAAHREHYRPTTGRSPVSRDVSFIGSAYWNRINFFRDIMPELMSYNTVINGIWWDRLPEAPIYGDRIEIGKWMSPQETAVTYSGSKIVINLHRSHIDEVANNNTLYIPAASPNPRTFEIAASGTLQLSDARDDMGSFYKVGEEIDTFSSPQEMMDKIRFYLTHEEERRDMALRAFERTLKDHTYTIRLNQLLTVIYG
>NZ_CP009280.1|WP_081970238.1|7044358_7045894_-|glycosyltransferase-family-4-protein
MAAPQPLAGERRDTMADKATIVLFSHVSNTRSITGAEKLLLFFSRELSPYFNCILVAPQDGKLTRLARSYGINVQLLSIPLVYGMYTPYAGLPADIRKLQESREYQELSDWLAGVRPSFIISSTCVHALPPMAAKSLGIPVVWKISETITDNEFTPISVELIHNNSDEILAISQTAAACFPEDIREGKVTQLPPSWNETEMMFEAWSKLRGERRSELKVAPEEPLIGYVSSFINKEKGLEHFVKMAVLVHEQHPAARYIVVGSPGDKSYYERCVRKVKLEGLTSRFRFVGYEECLPAAYCAMDLLVVPSLIREGFGMTALEGYAFGKPVVAYDSGGLREILNAAGCGELLVPAADIGALAERVNTLLAAPAMAAAIGSLARERIEAVYGPAAYRARLYGLAERWYLRYCLAPPQVSGAEEAPPAAPPAGGEDAPAAEAPRVRPSRRAARLRGAKLRRGRLRRAKAWARAAGTRPRRKKRAAGSARRKASGGGKHRRAGHARRRGRRRRKAG
>NZ_CP009280.1|WP_042139754.1|7043369_7043681_+|hypothetical-protein
MKDWLPGAVESGVVVPLIGAIPPGGADSGAFVLLVGAIPAGGANSGAFVPLIGAIPAGAANSGAFVPLIGAIPAGGANSGAFVILIGAIPAGGGGFRGSYPSI
>NZ_CP009280.1|WP_042139753.1|7042188_7043283_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MKIMTILGTRPEIIRLSVIIPLLDEHAERHVLVHTGQNFTASLSGIFFAELGLRAPDYVLQDKQAGLGGQLAAMFGSLESILLQEKPDRILLLGDTNSALCAILAERMGIPVVHMEAGNRCYDLKVPEEKNRRVIDAVSTINMPYTQQSKRHLLSEGFPSQRIVLTGNPIHEVITHYEEQIGSSDILSRLSLEAGRYLLVTAHRAENVDDPESLLQIMSGLNLVAEHYGLRLICSIHPRTRSKLTEQFPLTMNPLVEFHEPFGFFDFVHLERNALCAITDSGTVQEECCLMGVPTVTIRRTTERPETVDCGSNVVSGVEQNSILRCTRLMTSLKPAWEAPEGYLTPDVSVKVVKFLLGGNLHVQ
>NZ_CP009280.1|WP_042139752.1|7041212_7042199_-|NAD-dependent-epimerase/dehydratase-family-protein
MFNNKRILVTGGTGSWGHELIRQLLPQHPKEIIVFSRSESAQVAMSREFEDKRLSFVIGDIRDKDALVAACRGVDYVFHLAALKHVPVCEDQPYEALKTNVVGTQNVIEAAIANNVEKAIYISTDKAANPSNFYGMTKAIGEKLFVYANLIGSGTRFVTVRGGNVLGTNGSVVHLFMKQIKDKGQVRITDMNMTRFFFTLRDAITLLFKASEVSIGGEIFVMTMPTCRIVDLAEVLIEASGRRDVSMIEAGIRPGEKIHEILMSDFESLTTVVYDEQYLVILPTLDMPELKEHYREYPHVSFNSFSSENNLMDQAEIKDILIRGGFLK
>NZ_CP009280.1|WP_042139750.1|7040376_7041216_-|SDR-family-oxidoreductase
MKLLILGGNGMAGHMLADFFRRQGKHHVFHTTRDKNDLGGLYVDADDIAGVEKLVEIVSPHCMINAMGVLNQFAERDVIGAYHVNGFLPHRLRRAADSVHARLIHISTDCVFEGTRGGYTEEDATDGTSVYAITKSLGEVRDPGHLTIRTSIIGPEIRSGGIGLMEWFLAQKGRVTGYERVMWNGVTTLELAKVISSLLDSDLSGLIHLAHPRPVSKYELLQMMQSAFHKEDVKIIPERVHVQDRTLISTRSDVNFELPSYPEMLAELADFMHGSEMPT
>NZ_CP009280.1|WP_042139749.1|7039330_7040380_-|NAD-dependent-epimerase/dehydratase-family-protein
MKGRRLLITGAAGFTGRHAVAYFAAEGAEVTAVVRRCAAEASVFPAGVQQYICDLGDRKAVAGMIGEVMPDQVLHLAGKNSVPESWQDPLLYMETNVMATLYLLEALRFQPASRILVAGSRLKYRPDSAAGPPHPYSLSKTLEELVSLAWGTLFKQPVLMAEPSNLIGPGPSTGFCSLLAQHIVRSEAAAGRGEAPPAAFRISSRHVQRDFLDVRDAVRAYGYILDHGESGKIYRIDSGTQRELGEIAGKLLAHAAAPVEMDWGPQHAEEGQAAASPASAVPAKPSSASAASPASAVPVQPSSASADREVLQEEPEDNAAVLGWKPGIGLDRSLADIIGYTRAGKEGRI
>NZ_CP009280.1|WP_042141602.1|7038614_7039331_-|glycosyltransferase
MKPRVSVIIPFYNCPYIEQALQSALAQSWQPYEIIVVDDGSFMHAERITPYLPHIHYLGKANGGTASALNHGIAHSTGDYVVWLSSDDMFYRDKINNQVLFMEQNRLLITYTNFNFINGDSQLTQLNAAAVFHNQLDYLRCFLQGNPINGCTVMFKREIFGAIGLFNEALPYTHDYDLWYRAILNGYPPIMLNQSLTAYRRHDGMGTIKHYDVIMAEAAATNARYHAPLSSLIASMGG
>NZ_CP009280.1|WP_081970240.1|7050436_7050610_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein
MRNDDYKDKIEQARQELNKLALEHGMQDVRVLRQSVKLDALLNEYSDCNTEKDDQLY
>NZ_CP009280.1|WP_042139760.1|7050706_7052140_-|hypothetical-protein
MKKLNKAETLVALAGCVLILYLLFLKPFSGVADNGDFKRMMETVGLNYYDNTESYADRFFSYSHSRFSYENLFKGFYPSSQILVVLVPRLLAGLVHGSYFDIRLVACVYAMLLLWATWLLVKLGARGSYITGLLLGAGLLFVFYDIGYLAYFNSLFGEPVSMVFMLLTFALGLRLAGSERPPAGGLKLFFIAVLFLVCSKIQNAPVGLAFALIFLRLRTLNGTGNWRKLALRFAVATALVSVALYVAAPKELRHINLYQTVFFGILNGSPDVRGDLRDLGLPERLEVLAGTNYFQGDTAIKQDDPSLTTDFYNLVSHKDVLFFYLGHPSRLVENMKYAAKNSMSIRPYYLGSYEKSMGKPERAIDYTYSTWSQFKKNHLPHTLGFLVLFYLVYYAIVLAHYFRSRGRQARIAGEMMMLLGLIGLFSFLVPILGDGRADIGKHLFLFNVCFDMMAVAMFGWAVHKLVMLLKPVLAANR
>NZ_CP009280.1|WP_042139761.1|7052156_7054055_-|LTA-synthase-family-protein
MNDKKHVPVQAHFYIVIGLVWLKLLLLRGLFFDRIAWEWIAADIAPVLLMMGVLALITPVRMRKAVFWGFNGLLSLLFFAASVYFNHFGSVPTYLALYELNQVFQVKESVESTIELIDYLFFADLVIMIIYLLFRRWKNGPVQQQRGSQPSRRARRVYLIALLVAIIGGGSLSAYSIDSARGITNELVQAESAGFLNYEVVAAIKAQEDNGLIGTGDINETIAKVEALEAAYPYKDIAGGLPEYFGSQKGKNVIVIQMEAFQNFPLHQSLDGQELTPVLNGLAGEGFYFPHVFQQVGPGNTSDAEFMSNTSVYPIATLAMSTGFGDRELPGLPRLLRDKGYEAYTFHVNKVGFWNRNELYPALGFNGYYDKGYFKNDHFNAFGASDEQLYATAVEKLAALQKKGTPFYAQLVTASSHHPFQIPDSFKKIKVPEDLQGTMLGDYLTAVNYTDYAVGTLIDGLKQQGMWDDTVLVLYGDHFGLQPKDVPAEQVEEALGTPYDDRISRFNIPLIIHVPGMEQGQVVERTGGQLDVLPTVANLLGVSLKDEGFTAFGHDLLNIDSNVVGMRYYLPTGSFFNDEVMFVPGKSFADGEAISLDTYEPVEDFSKYQTDYDYILKLMGLSDEYVKLLPQR
>NZ_CP009280.1|WP_042139763.1|7054245_7055469_-|hypothetical-protein
MDKREQEPQWYEQARKGPFPEMKFTEEAAGKVARQIGMDGSSLNQVLPSGRRRRAIRLRILSAAVILLLFGAGAVYWGSGWSGQHGGFNPLQVSSTGIIDPPVAEQADLTDEGFRETAEQVMQEQLGKKLPFVNLEPLVEEGETLADFKDGDSFAKIWFETETGKVVRTYMDTFFAPEQIDSKFIDEAMDQLRKAGYKGEFTVTALHHSVHYGTNADEQGIQTDDSLIAEEGQIDYENGVYRSSTFKMGENEVSAEVKQAGLKAIKLLREKGTDHLYSIKRTVAQKWDVLVLTYGESERGATTVMMDYATQDILQVFDVSLYDEKSFSSADPNTNLLDMDKAKFQRSAAAIADEMFGIRLGEYTIVKEMSGIGSIAFKSPDGATIITGSYNLDGTFYMIQQTPATAE
>NZ_CP009280.1|WP_042141606.1|7055468_7055978_-|RNA-polymerase-sigma-factor
MKLYGEDVWNYIYFLTKNSDQADELTQEVFIKCFYRIGTYRGISSLKTWLFTIARNTVFSYRKSRFFRSGLWGGMQPLPATAQHRKEAAGQAVVARSAEMEYLGNRQVDEIWSMIMKLPDKLREVLVLDLKAELSVREIAELIRISPGTVKSRLHRARHKIQDKLRRME
>NZ_CP009280.1|WP_042139764.1|7056591_7057929_-|5'-deoxyadenosine-deaminase
MANILIKHAEIITMNKQEEIIYGDIRIKDNLIVEIGSGLEVQGDETVLDAKNRTVIPGFVQTHIHLCQTLFRGKGDDLELMDWLRKRIWPLEAAHDEESLYYSAMLGIGELITSGTTTIVDMETVNHTDFAFQAIAKSGIRALSGKVMMDQKNADAPAALQEDTAASLQESVDLLEKWNGYGNGRIQYAFSPRFVISCTEPLLKEVRNLSEHYGVKVHTHASENLGEIEIVQAMTGMRNVVYLDHLGLANERLILAHCVWLDEEEKRILRDRGVHVSHCPGSNLKLASGIADTPGMLHDHIHLSLGADGAPCNNNLDMFNEMRLAAVIQKPQHGPTTMDARSVFRMATIGGAKAVGMEDQIGSIEVGKKADLAILNLYNFHTFPSYDVDPISRIVYSATRADVETTIVDGQILMHKGLLKTVDKETVLHEANRSIKRLLVNTPLG
>NZ_CP009280.1|WP_156118801.1|7058230_7058752_-|GNAT-family-N-acetyltransferase
MGNEIRRAQSNEIGEIMDLIAKCVQVMQAGGSDQWDESYPNREIIAADIATGTLFVCLDNEAIAGIIVLDENQAEQYGAIEWLQQQGPHLIMHRLAVHPEFQGKGIARQLIAFAEEHARHSGYSSIRMDTYAKNERVLKIYPSLGYVQRGEIHFPGRVAAFPVFEKVLTEIFG
>NZ_CP009280.1|WP_039307029.1|7058938_7059151_-|hypothetical-protein
MHVVQPPVQVVPAVEAPPVAQVVPLPPDLGVPPELPPGDAFQQGYTEAYNVGFDAGFAKGFEDGHKLELG
>NZ_CP009280.1|WP_042139766.1|7059363_7059654_-|hypothetical-protein
MSGGLLSEHAVKLEMIRSIARSQAALAAILESIAEVTGQSELTARKLSDNIRILSGYQSSMCRMISGISLHEPKQGVPAAPWLSKDCSEGTAARSR
>NZ_CP009280.1|WP_039306867.1|7059650_7059992_-|hypothetical-protein
MSREKAYLQMLESTAVIQWNIAMILEAKAVEAEKVKQWTHHHIHARAFDSHEDQLKESLSIHEVIVEMVEGLTKLENGLYSNLKAVLGSGEDEGGGDFGGDGGDGFSFGDDSK

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_CP009280_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP009280_20

7540896-7540970

Orphan

Consensus_repeat	Method
GATTTAGTGGGATTTATCCCTTTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP009280_20

>merge|NZ_CP009280|20|7540896-7540970|CRISPRCasFinder
GATTTAGTGGGATTTATCCCTTTAATCCCGCCGCTCAACCCACTTCCGGCCGATTTAGTGGGATTTATCTCTTTA

>NZ_CP009280|20|18|7540896-7540970|CRISPRCasFinder
GATTTAGTGGGATTTATCCCTTTA	ATCCCGCCGCTCAACCCACTTCCGGCC
GATTTAGTGGGATTTATCTCTTTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP009280.1\|WP_042140063.1\|7552128_7553739_-\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223981
NZ_CP009280.1\|WP_042140048.1\|7525973_7526990_-\|glycosidase	unknown	unknown	gnl\|CDD\|350126
NZ_CP009280.1\|WP_042140051.1\|7532719_7534330_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270299
NZ_CP009280.1\|WP_042140056.1\|7541138_7541816_-\|deoxyribose-phosphate-aldolase	unknown	unknown	gnl\|CDD\|234784
NZ_CP009280.1\|WP_042140054.1\|7536605_7539362_+\|alpha-mannosidase	unknown	unknown	gnl\|CDD\|223460
NZ_CP009280.1\|WP_042140046.1\|7521907_7523017_-\|amidohydrolase/deacetylase-family-metallohydrolase	unknown	unknown	gnl\|CDD\|132622
NZ_CP009280.1\|WP_042140050.1\|7530383_7532687_-\|beta-glucosidase	unknown	unknown	gnl\|CDD\|185053
NZ_CP009280.1\|WP_052422114.1\|7547127_7549404_-\|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl\|CDD\|274362
NZ_CP009280.1\|WP_144026171.1\|7543901_7545290_-\|STAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|223732
NZ_CP009280.1\|WP_042140052.1\|7534368_7535280_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP009280.1\|WP_042140053.1\|7535296_7536247_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_CP009280.1\|WP_042140061.1\|7550158_7550833_-\|DUF2294-family-protein	unknown	unknown	gnl\|CDD\|378372
NZ_CP009280.1\|WP_042140057.1\|7541943_7543701_-\|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl\|CDD\|223910
NZ_CP009280.1\|WP_039297374.1\|7551787_7552132_-\|ferredoxin-family-protein	unknown	unknown	gnl\|CDD\|224069
NZ_CP009280.1\|WP_042140062.1\|7551121_7551667_+\|glutathione-peroxidase	unknown	unknown	gnl\|CDD\|238207
NZ_CP009280.1\|WP_042140059.1\|7545553_7546630_-\|3-deoxy-7-phosphoheptulonate-synthase	unknown	unknown	gnl\|CDD\|183614
NZ_CP009280.1\|WP_042140047.1\|7523265_7525602_+\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP009280.1\|WP_042140060.1\|7549619_7550009_-\|response-regulator	unknown	unknown	gnl\|CDD\|381100
NZ_CP009280.1\|WP_042140049.1\|7527212_7530380_-\|alpha-mannosidase	unknown	unknown	gnl\|CDD\|223460
NZ_CP009280.1\|WP_042140055.1\|7539391_7540672_+\|glycoside-hydrolase-family-125-protein	unknown	unknown	gnl\|CDD\|377716

Protein	Function_ID	Function_description	E-value
NZ_CP009280.1\|WP_042140063.1\|7552128_7553739_-\|FAD-binding-protein	gnl\|CDD\|223981	COG1053, SdhA, Succinate dehydrogenase/fumarate reductase, flavoprotein subunit [Energy production and conversion].	2.62543e-52
NZ_CP009280.1\|WP_042140048.1\|7525973_7526990_-\|glycosidase	gnl\|CDD\|350126	cd18614, GH130, Glycosyl hydrolase family 130; uncharacterized. This subfamily contains glycosyl hydrolase family 130 (GH130) proteins, as classified by the carbohydrate-active enzymes database (CAZY), most of which are as yet uncharacterized. GH130 enzymes are phosphorylases and hydrolases for beta-mannosides, and include beta-1,4-mannosylglucose phosphorylase (EC 2.4.1.281), beta-1,4-mannooligosaccharide phosphorylase (EC 2.4.1.319), beta-1,4-mannosyl-N-acetyl-glucosamine phosphorylase (EC 2.4.1.320), beta-1,2-mannobiose phosphorylase (EC 2.4.1.-), beta-1,2-oligomannan phosphorylase (EC 2.4.1.-) and beta-1,2-mannosidase (EC 3.2.1.-). They possess 5-bladed beta-propeller domains similar to families 32, 43, 62, 68, 117 (GH32, GH43, GH62, GH68, GH117). GH130 enzymes are involved in the bacterial utilization of mannans or N-linked glycans. Beta-1,4-mannosylglucose phosphorylase is involved in degradation of beta-1,4-D-mannosyl-N-acetyl-D-glucosamine linkages in the core of N-glycans; it produces alpha-mannose 1-phosphate and glucose from 4-O-beta-D-mannosyl-D-glucose and inorganic phosphate, using a critical catalytic Asp as a proton donor.	2.65915e-113
NZ_CP009280.1\|WP_042140051.1\|7532719_7534330_-\|extracellular-solute-binding-protein	gnl\|CDD\|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.13528e-131
NZ_CP009280.1\|WP_042140056.1\|7541138_7541816_-\|deoxyribose-phosphate-aldolase	gnl\|CDD\|234784	PRK00507, PRK00507, deoxyribose-phosphate aldolase; Provisional.	7.95981e-120
NZ_CP009280.1\|WP_042140054.1\|7536605_7539362_+\|alpha-mannosidase	gnl\|CDD\|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_CP009280.1\|WP_042140046.1\|7521907_7523017_-\|amidohydrolase/deacetylase-family-metallohydrolase	gnl\|CDD\|132622	TIGR03583, EF_0837, probable amidohydrolase EF_0837/AHA_3915. Members of this family of relatively uncommon proteins are found in both Gram-positive (e.g. Enterococcus faecalis) and Gram-negative (e.g. Aeromonas hydrophila) bacteria, as part of a cluster of conserved proteins. These proteins resemble aminohydrolases (see pfam01979), including dihydroorotases. The function is unknown. [Hypothetical proteins, Conserved].	2.05082e-170
NZ_CP009280.1\|WP_042140050.1\|7530383_7532687_-\|beta-glucosidase	gnl\|CDD\|185053	PRK15098, PRK15098, beta-glucosidase BglX.	0
NZ_CP009280.1\|WP_052422114.1\|7547127_7549404_-\|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	4.12043e-99
NZ_CP009280.1\|WP_144026171.1\|7543901_7545290_-\|STAS-domain-containing-protein	gnl\|CDD\|223732	COG0659, SUL1, Sulfate permease and related transporters (MFS superfamily) [Inorganic ion transport and metabolism].	2.03536e-129
NZ_CP009280.1\|WP_042140052.1\|7534368_7535280_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.37997e-66
NZ_CP009280.1\|WP_042140053.1\|7535296_7536247_-\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	8.99304e-128
NZ_CP009280.1\|WP_042140061.1\|7550158_7550833_-\|DUF2294-family-protein	gnl\|CDD\|378372	pfam10057, DUF2294, Uncharacterized conserved protein (DUF2294). Members of this family of hypothetical bacterial proteins have no known function.	2.54404e-14
NZ_CP009280.1\|WP_042140057.1\|7541943_7543701_-\|methyl-accepting-chemotaxis-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	8.16816e-41
NZ_CP009280.1\|WP_039297374.1\|7551787_7552132_-\|ferredoxin-family-protein	gnl\|CDD\|224069	COG1146, COG1146, Ferredoxin [Energy production and conversion].	1.14291e-10
NZ_CP009280.1\|WP_042140062.1\|7551121_7551667_+\|glutathione-peroxidase	gnl\|CDD\|238207	cd00340, GSH_Peroxidase, Glutathione (GSH) peroxidase family; tetrameric selenoenzymes that catalyze the reduction of a variety of hydroperoxides including lipid peroxidases, using GSH as a specific electron donor substrate. GSH peroxidase contains one selenocysteine residue per subunit, which is involved in catalysis. Different isoenzymes are known in mammals,which are involved in protection against reactive oxygen species, redox regulation of many metabolic processes, peroxinitrite scavenging, and modulation of inflammatory processes.	1.30111e-91
NZ_CP009280.1\|WP_042140059.1\|7545553_7546630_-\|3-deoxy-7-phosphoheptulonate-synthase	gnl\|CDD\|183614	PRK12595, PRK12595, bifunctional 3-deoxy-7-phosphoheptulonate synthase/chorismate mutase; Reviewed.	0
NZ_CP009280.1\|WP_042140047.1\|7523265_7525602_+\|AraC-family-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.45038e-23
NZ_CP009280.1\|WP_042140060.1\|7549619_7550009_-\|response-regulator	gnl\|CDD\|381100	cd17548, REC_DivK-like, phosphoacceptor receiver (REC) domain of DivK and similar proteins. Caulobacter crescentus DivK is an essential response regulator that is involved in the complex phosphorelay pathways controlling both cell division and motility. It localizes cell cycle regulators to specific poles of the cell during division. DivK contains a stand-alone REC domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.00851e-36
NZ_CP009280.1\|WP_042140049.1\|7527212_7530380_-\|alpha-mannosidase	gnl\|CDD\|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_CP009280.1\|WP_042140055.1\|7539391_7540672_+\|glycoside-hydrolase-family-125-protein	gnl\|CDD\|377716	pfam06824, Glyco_hydro_125, Metal-independent alpha-mannosidase (GH125). This family, which contains bacterial and fungal glycoside hydrolases, is also known as GH125. They function as metal-independent alpha-mannosidases, with specificity for alpha-1,6-linked non-reducing terminal mannose residues. Structurally this family is part of the 6 hairpin glycosidase superfamily.	0

>NZ_CP009280.1|WP_042140055.1|7539391_7540672_+|glycoside-hydrolase-family-125-protein
MKLPASITTYLTEADERLAHHPKLQQLFRNCFPNTLETTTKLLNDGTTFVFTGDIPAMWLRDSTEQVRHYIPFAKNDPELQRILRGLIARQMFYVNIDPYTNAFNETASDKHYRDTDDCNLNPWMWERKYELDSLCFVVQLAYMYWKEAEQTDIFDTACYQALTSIVNVIETEQYHGEKSPYHFIRQTLQDTETLYNNGRGMPVNYTGMSWSGFRPSDDSCEFGYNIPSNMFAVVILGYIREIASEVYGDERLAARAAKLRKEIDFGIRTYGIVTHPKYGRIYAYETDGFGNYSLMDDAGTPGLMSIPYIGYVGVEDEIYQNTRRFALSFDNPFYFEGKHAKGIGSPHTPGGYVWHMALSMQALTADNDEEIKELIDMLIRTDADTGYMHEGFHPDDPSDFSREWFAWSNSLFATLISKAMDKGLV
>NZ_CP009280.1|WP_042140054.1|7536605_7539362_+|alpha-mannosidase
MTRTTAHLISHTHWDREWYMPYERHHVLLAKLMNELLETLEKDERYRYFHLDGQTIIIEDYLQVHPEKRELLERFIREGRIVIGPWYVLQDEFLTSSEANVRNLLTGHQDAAKYGVISKLGYFPDSFGNMGQAPQLLRQADIGTAVFGRGVKPTGFDNMVGELTSTSYESPYSEMFWESPDGSSVLGLLFANWYSNGNEVPVDAGEAKIFWDKKIADAGKYASTPELLFMNGCDHQPVQRDLADALETARELYPDTDFVHSSFEQYLHALGPSLPEDLVTVTGELRSQHTDGWGTLVNTASARVYLKQLNQRGQTLLEKGAEPLATLAYLVSGQAYPHALLTYAWKTLMQNHPHDSICGCSVDEVHREMITRFEKSRHVGEAIIEESLKAVSGQIGTKDVDAWGESAIPVTVFNTTGWERSGTVSVEVIFAKRYFKEGPNPAAIAEALDQLPRVLERGRLLDADGRVLACKAEDLGTRFGYELPDEQFRKPYMARIVRLTFEAAQVPPLGYTSFAWVQLPGGESAGAAASPLALTKTGMENGFLAVLIREDGSYDVTDKRTGKTFTGLGVYENCGDIGNEYVFRQPEGDTPLTTRGLDARITLAEHEPYRITYEIVHEWTIPASADASFAEEKRRMVPFRQRKAGRSSEQIPLRIVTRISLEANGTGVLVSAKFNNQAMDHRLRVLFPTGLAASTLLADSVFEAAEREIEPAQGWLNPSNAQHQQAFVSVSDGSAGVVIANKGLNEYEVLRDGRNTIAVTLLRSVSELGDWGVFPTPEAQCLGEQTVEFAVRPYAGDAAQPEAFAWAYQYQVPWFAVQTGWQEGSLPAEYQPLKWQGRTLALSAFKLSEAHEDIILRWYNLAHTEQPIVLEPHFPVQAVHASDILERRKHRELLDEGILRSSVGKAQIVTYALQAVQP
>NZ_CP009280.1|WP_042140053.1|7535296_7536247_-|sugar-ABC-transporter-permease
MKGSNAAVSGNPSLKNKSLGKRIWQNWELYLFMLPALLYFLVFHYGPMYGIQIAFKNFVPSKGITGSEWVGFDHFERFFNSYFFWDLLWNTFSISFYELAIGFPLPIILALAFNEVRNGPFKKSVQTVTYAPHFISVVVMAGMIITFLSPSSGMIVRAIEFLGLQPAEFLTDPAWFKTVYVFSGVWQSTGWGTIIYLAALSGVDPQLHEAAIVDGASRIKRVLHINLPTIIPTITIMLILNMGNILGLGFEKILLLQNSLNMEASDVISTYVYRAGLVNAQYSFSTAVGLFNSVVNVILLVTVNRIAKRTSENSLW
>NZ_CP009280.1|WP_042140052.1|7534368_7535280_-|carbohydrate-ABC-transporter-permease
MVTAMKESRGDKLFLISTYIYLFLALLVVLYPLIYILSASISSPQDVNSGAMWLFPKNVTLDGYKLVFENPKIWNGYWNTIVYTVAGTLLNLAVTLPASYALSRSDFVGRQLFMGLILFTMFFSGGLVPTYLLVKNLGLINSMGALILPVAASVWNIVVARTFFQTTIPKELQEAAHIDGCTNLGLFIRIILPLSAPIVAVMALFYGVGHWNSYFPSLIYLNDEAKYPLQMVLRQILVLQEMSAETTGAAINGEVAMAMNNKAETASLVKYGVIVVSTLPIVAVYPFLQRYFVQGVMIGSVKG
>NZ_CP009280.1|WP_042140051.1|7532719_7534330_-|extracellular-solute-binding-protein
MQTTRKPWKLLLSSAVILTLLAGCGNSNEGAANNSTGEVTVNKEGFPIVTEPVTLTLMAPDVGIQNWENMAVLQQMQEKTGITLEYKNAPKDSFETKKNLVFASGDYPDIFYAAGLTTAEQMNYGEQGILIPLEDLIEEYAPNFKALLEENPDVRKSITAPDGHIYSLPVVEFSQHWYRNPMWYNGDFLKALNIDKLPETTEELYTYLKRVKEEDPNGNGTADEIPISSVTTAAANLRDIRTWLLGAFGIYEEEIYVDDADKVHYTPLEEGYKEYLTYMNRLWSEELLDHESFSQTAEQKKAKAQNNRVALFSDWHAYMTKGGEPSTTDPMFAPVRSESVAAPAIAKNRGITTGAFAITNSNPEPEASLRWVDYLYSYEGALFFNKGPEGVLWEYTDKDNRVKQYLPVPDGKEMEDYRATLTPNYGIPAPTLSMDDINKGLKTDFDLWVEQETKQKLLDKGARIPFPALFLTVEEQTEISSLNSDLSTYVKQMEAKFITGAEPLTGWDNYVATVKKMGGERVAEINQAAYDRWKSN
>NZ_CP009280.1|WP_042140050.1|7530383_7532687_-|beta-glucosidase
MIYKDKTRPVADRVQDLLQRMTLGEKAGQLVQPFGWQCYEKRPDGTTGMTEAFKRQVAAGGVGSLYGTLRADPWTGVTLETGLSPKQGAEAVNAIQAYAMQESRLGIPILFGEECSHGHMAIGATVFPVPLALGSMWNPELYREMCRVVALETRSQGGAATYSPVLDVVRDPRWGRTEETFGEDPFLIAAMGVEAVKGLQGERLDAEDSVMATLKHFAAYGSSEGGRNSAPVHMGLRELHEVDLLPFRKAVEAGALSIMTAYNEIDGVPCTTNRYLLQDVLREQWGFDGFVITDCGALGMLTNGHNTADSGEAAVAQALLAGIDMEMSGEMFEKHIADAIDHGRLQEYDLDRAAARILELKFKLGLFDRPYADPEQAERTIGKPEHRELARRIAGESIIMLKNENGTLPLSRRIPKLAVIGPNADAPYNQLGDYTSPQPKGATVTVLEGIRQALGGNADNVLYAPGCRIKGDSREGFAHALACAAEADAVVLAIGGSSARDFGEGTIDLLTGASVVTEHSWSDMECGEGIDRATLNLMGVQLELAQAIHKLGKPLIVVYINGRPVAEPWIVEHADAILEAWYPGQEGGHAIADILFGDVNPSGRLTISIPKHAGQLPVYYYKRRTRGKRYLETDFNAEYPFGYGLSFSEFKYSNLKVEPSVITADGEALVSVDVTHSGDRAGSEVVQLYISDLASAITRPEKQLKGFRKISLQPGATKTVTFSVGREQLEYVSADLTRIVEPGEFTIMAGPHSAEYLTAPLHVREEG
>NZ_CP009280.1|WP_042140049.1|7527212_7530380_-|alpha-mannosidase
MKRMNRFIEWLAKRQWTEKVELAEWNMRKSRYLSPGNYEHEEELHLNYRIARLDGGYGTTYFLQREITVPGDWGPEESALLYLGRGEGLLKLNGAPYHGLDSNHWFIPLPPGTAGEVLQLDIELYDPVPEPEDPLNRQAVIKPPLTGVEITLVRVNLAVYSLLHTVKIVHEAALLLPEGDMRRIRSLKALERVMDTLYMKEPLLLDGAAVTAAEQQLRTEAAAERSAGLHPGTMHMVGQSHIDIAWLWPVRETVRKVSRTFSTVCVLMNRYPEFRYSQSQPQLYAFAKEHYPQLYGRIKERIAEGRWELVGGMWVEPDLNIPGGESLVRQMLYGQGFYMKEFGKRSTIEWLPDTFGYCASLPQLLKQAGIDYFMTTKLGWNDTNPFPHTLFHWVGIDGTKIVAYQNHGVNEHTHPKDVQEHWQAYAQKEQHDELMLLYGHGDGGGGVTHEMLEYVSRTGLAPGQPVSKFSTAEAFFSEIGLRQPGLPAWHGDLYLELHRGTFTTHAFNKRSNRKAEVLYRQAEIWSVLAQKRGLPEPAQPELKLLLKHQEELAEGWKLLLLNQFHDIIPGTSIPEVYATSREQYADIFSIGQRVLDTSLRALASKVNTTGEGRPYVVFNSLGWERTELIRLEGDRSLAALQAFDEDGLLDSEGWSTDEDGGSYTLVVRVRKVPAFGCRTFWLREAAAPAGEQPGRQAEPVSVDGFPEQWETDHYILNFNEHGEISRWVDKSAGRELLQPGQTGNQLQFYHDTPPLWDAWDLDPRYEEQPAGKAKLLDRQVVTSGPVLTVLKFRWQLNESLIEQEIILPRHSRRVDFRTNVSWREQHKLLKVAFPVDIVAAKATYEIPFGALERPTHRNTSWEQAQFEVCGHRWADLSEGGYGVSLLNDCKYGYDIHDGVLRLSLLRSPRWPDRNADQGEHEFTYSLYPHGGEWRQADVVREAAELNEPVQVIGEQPHSGRYSSTYAWLNFQSSHVMLDTIKSAEDGSGVIVRMYESAGSRGTAALDWKDANIRACRVNLLESETGTLETSGGAASLSFRPYEVQTVKLYKKHERN
>NZ_CP009280.1|WP_042140048.1|7525973_7526990_-|glycosidase
MQITRHPNNPIVVPGGYEWRKVTVFNPAVIIDNGKFYMIERTAGSLTPCKNYLGLLESEDGVSFTHVKDEPIVTPDMLGFPYGSVQDPRIVKIDGTFYLNYALRPCAMSYYPTGAGVPQRSIPEYPDGWGEQEGHWLTRSSILKSDNLLDWEFVADTTPLDINDRDNILFPEKIGGKFVLLRRPEEYVGEAYGTEKAAMWITYSEDLVNWEEPKLLATAGNLSWESRKIGGSSPPVRTDKGWLVLYHGVDEDIVYRVGAMLLDLEQPEKIIARTHNFIMEPETYYEKFGFQIPNVIFPTGNVVKDGLLYIYYGVTDTAIALATVPLDELVEHILQEAQ
>NZ_CP009280.1|WP_042140047.1|7523265_7525602_+|AraC-family-transcriptional-regulator
MANPALKPSLLNRFRLSWNHFKSRLLLKYAFSYILMFLIPLTGVTIFVYENAVKGLRVEIEQSNVNQLNQVKSTIDDRMNELQEISGRIAYDKHLTPYMVRHPYYSLEAIQALANYKASSSIAEDLLLYFHDDSNIYSYRGLADLHVTFDTLYQFERWTPEDLRRDLNETRQPLVRPAENVTVNSRVEPMLVMLVPIKPNDPFPYGTVVYLLKESNLTGVMDSILSDFSGSSYIFGASGEVLTANSHDVSLPQDELENLSALEPGIHNLELDGEQYSVVSVKSEENGWTYVTTMPSFQFFSRVAHVQTLILIVFCITVITGIAAALLLAKRQYHPIRDLMEFAKLRSSGNDTSKLRNEWEWIRQTLHDYSARIDLQEPFVRNQCMLLLLKHGKPDDPEIEQMILSAGFSHPQGQGLYFSAILSWDEPVPGGKSWQERHQLQEMLSNVSIPGPDAQIFGVEFSVKDQFALIISLPGEEDMPVQSRMEQVIEAIQAVIREHSQLALSIGVGMAYRDLARLNQSFIEAAAALEHRMIRRSGQVTYFEQLAELNPSAAESFWIPRKSMLKLEQSLKQGNESVAVQMIADTIDTIKGEPLQVHLLRCICFDLLNAFLRTASELGMDEVFANMPELTSFETLEELESRLLVLAAAICAQVERNTETSESSLMDDILAYVDQQFADYTLSLEHVALKFAISTSYLSRSFKEKTGSNFSQYIWQRRVDEVIRLLVNTSSPLKEIIEQVGYLDAPNFIRKFKKETGLTPGQYRKEHALKGAAAKRPV
>NZ_CP009280.1|WP_042140046.1|7521907_7523017_-|amidohydrolase/deacetylase-family-metallohydrolase
MGRVGTENVLRNLQLVGGQRVDIAIQDGVITAITPPGQAEGEHSMDCSGLYVSSGWIDLHVHAVPELDPYGDDIDEIGVKQGVTTLVDAGSCGADRIGDFYTGSLKAATRVFALLNISRIGLERTDELSQLEWIDRSKALEAAAAYPEFIVGLKARISQSVVKDSGIQPLKLARALSEETKLPLMVHIGSAPPAVTEVLELLQRGDVITHYLNGKSNNLFHEDGTPLQELLDAAARGVHLDVGHGTASFSFRVAEQAKAAGIALNTISTDIYRGNRLNGPVYSMSNVLTKFLYLGYSLEEVIRAVTSSAAEWLGKPELAQIRVGQQANLTLFAVEAGGKQLKDSEGDVRAAHYYIEAKGVYANGSLITG
>NZ_CP009280.1|WP_042140056.1|7541138_7541816_-|deoxyribose-phosphate-aldolase
MSETTISGIIDHTLLKADARKDDIIKLAEEAKAYKFASVCVNPAWVSTAHAVLKDTPEVKVCTVIGFPLGSSTPETKAFETTDAIANGAGEVDMVINIGALKDGNDELVKRDIAAVVEAARGKALTKVIIETCLLTDEEKVRACKLAVEAGADFVKTSTGFSTGGATKEDIALMRATVGPAIGVKASGGVRSAEDALVMVGAGATRIGTSGGVAIAKGEQSQSSY
>NZ_CP009280.1|WP_042140057.1|7541943_7543701_-|methyl-accepting-chemotaxis-protein
MFSFIRTRLIARILCIMTVVILCITAGNIAIQRANTGSAVKGTISSYNMSIASHYVTQIDAGRYSEFLADPRESDLYWSLRNELDQFRVSIGARYVYFVRIDEANQPQLMIDGRPEGDPLASQINEITDMPAAAVEAVLAGENASTPLIMNPEYGDYISAFVPVKGADGALIGALGIDTDVAVLSSLTRDVLIQSLPLYGIILALSLAALAVLAWFVSRSLRPLGTITQSAGTMARGDLAEAARILNARPVRSRDEIGTAYQAMLQMSGDLNARVRGMVSGVSTASDSLYGSSETFARNADDVLKMSEAVNGRIGDIYAGAHSQTEGAQSSAVAMDEMAQGISRISAASAVVSEFAVKALDIVQSSQTAMNHTNQQMKSISVSTGHTLDIVLLLQGYANEIEGALAAIRQFADQTKLLALNASIEAARAGEHGRGFTVVAGEVRKLAEGSAASVERVADLLIHIGNASASIGTQMTDASHEVSEGVRMSAEAEAALLEASAAFREVAGQIVDMSATAEQLSAGTEEVAATVGSMASIAGGVSEQTRQIRELTGLQLEKIKEVYEASMMISANTGDLREAIRQVKV
>NZ_CP009280.1|WP_144026171.1|7543901_7545290_-|STAS-domain-containing-protein
MTVAIALIPEAIAFSILAGVSPMVGLYASFCIAIVTAFAGGRPGMISAATGAMALLVGSLVISHGIEYLFAATVLAGIFQILMGMLKLGRFITFLPQPVMTGFVNALAILIFMAQLVHFEGQGWIMYALVALTLVIIYTVPRITKAVPSALVAIIAVSVLSIVLNLDVRTVGDMGTITSALPVFHLPDLPFTLDTLLIILPYSLSLAVVGLLESLMTATLIDDITGTGSDKNREAKGQGLANIVTGFFGGMAGCAMIGQSMVNMKSGGRTRLSTFVSGIFLLFLILVLGDVVKQIPMGALVGVMIMVCISTFEWGSLKTLAKVPLSDALVMIVTVVTVVVTDNLSIGVLFGVLLSALSFAWKMASIKLGVHTTASVTTYKVSGQLFFGTTSHFVHEFMYESDPQQVIIDFSHSHVWDQSAVGAIAKTLDKYAALGKKVTITGLNEESARLVKRIGLSLSGGH
>NZ_CP009280.1|WP_042140059.1|7545553_7546630_-|3-deoxy-7-phosphoheptulonate-synthase
MSNVELDKLRARLDEINGQLLELISERAEIVQEIGVLKEKQGVPKFDPEREKAMLDKLVASNKGPFTSGTIRTLFKQIFSASLDLQSTEHKKSLLVARKNHAEDTVITLPGNVTVGGLSSLMVAGPCSVESELQTRTVAAALQKAGVKVMRGGAFKPRTSPYDFQGLGMDGLRILREAADEYGLLTISEIVDPRHIEEALDYVDVIQVGARNMHNFELLKAVGEVNKPVLLKRGLSATLDEFVHAAEYIMSRGNMEIILIERGIRTYEKATRNTLDISAVPILKQECHLPVLVDVTHSTGRKDILIPCAKAALAAGADGIMVEVHPDPATALSDAAQQLNIEEFNTFFNEVKASGLYR
>NZ_CP009280.1|WP_052422114.1|7547127_7549404_-|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator
MLRQHTESSSPFEQAFKKGTAGVAFLSISEEWTSVNPAVTLLLGYMEERLLGHGFAEFLSEDSLEIHRQKMGTLKAGEAPFFECELNFRHADGSVVAVLLHVSLISEPSTGMGLYYIVHLAGLPHTEAKSRNELPAPPDELYRLIAANIRDIVYYATPDGICRYCSPSIVEVLGYKPEELIGCDIRGLVHPGDMEFMSAPQAAELQSVQLRILHKDGRYLWIEFTLRIVEDSGNWSVLAVGRDVTQRKIMEQKLQESVERYTSLKKYNHDAIISLDLEGNIINGNEKAVELTGYTIPELVGMSVGRIIGNHHLHDVISFCQKKGSMERSIDLIWHKDGHSVEVLTTLAPIIINNETVGFYIIVKDITEQKKLLIAKETAENTNRAKSEFLAMMSHEIRTPMNGVIGMTDLLLDLSDPDSQQREYLEIIRQSGESLLNIINDILDLSKIEAGKTSLHEEPFVLQHCMESALELLQLKAENKGLAIQVEVGPDVPADLIGDGERLKQILINLVGNAVKFTHTGGVKVGVQRIRGEEAADGVTLQFTVADTGIGIPEDARSRLFEPFYQLDHYMSRKHEGSGLGLAISKQLVEMMGGRIQLEPQTGQGATFVFTVVLRTEKQAQTAEGAEPGLLSPQQLSRSLRILVAEDNVINQIVLRKILEKRGFAVDVAEDGLQVVEMVTQRSYDLIFMDVQMPGMNGLEATSRIRQTQPADSQPVIIAVTANALKGDRELCIEAGMDEYISKPLRSETIVNVIGKFF
>NZ_CP009280.1|WP_042140060.1|7549619_7550009_-|response-regulator
MEEYKRTVLYVEDNQLNMALMHHIFKRNLPSVLLLKAETAELGLSIAREALPDLIILDIGLPGLNGYEALEILQQDEATCHIPVLGTSAFAQLSDIEKARNKGFAAYITKPFQVKAFTEMVKRLLDGGL
>NZ_CP009280.1|WP_042140061.1|7550158_7550833_-|DUF2294-family-protein
MSTTELTSQLSSFTGRLLRERFGKGPESIHASIGKQCIALHIRNFIGPVERFLLNKEEEQAFRYTRELLMKSLLPELAAYLKETMAMEVGELFYDWGIHNASGMIVALIKNDVMVIDDYAGRQEVHAQINEVSRKVQKEPVYTDSWWLGPRILIIKREGILIPLEKELIGLGYENTLKTTKRKMEKRYLEDTTTIAPMLGKELSDIYVDWDFDKDTSVIAYTFQ
>NZ_CP009280.1|WP_042140062.1|7551121_7551667_+|glutathione-peroxidase
MSIYEYEARNIRGKETRLEQYKNKVLLIVNTASKCGYTPQYSDLQKLHEKYQEQGLQILGFPSNQFGEQEPGSNEEVNVFCQINYGVTFPLFEKIDVKGDNRHPLFAYLTEQAGFQGFDDTDSNGKLLHTMLQERDPAALTNDEIKWNFTKFLIDRNGNVVERFESPVDPLDMEPAIQKLL
>NZ_CP009280.1|WP_039297374.1|7551787_7552132_-|ferredoxin-family-protein
MIELVSQDRCIGCRLCVKVCPTNVFEMQGKLAVIARQEDCQTCFMCEAYCPADALYVAPQADLSMEVDEQELIESGLLGSWRAEIGWNPGAEDTMAERDTTPFFEVFTETYRGK
>NZ_CP009280.1|WP_042140063.1|7552128_7553739_-|FAD-binding-protein
MPQQQQQATTDVLVLGGGPAGAWAAWSAASQGAKVILADKGYLGTSGATAPGGTTLLVIQPVAELREQAVQARLKAGGYLSENAWIHRVLDQVEQNLELVEEWGYPFPKDEEGRPLRTHLHGPEYMKLMRKVVRKAGVRIWDQSPALELLHDQHGVGGARGINRLTGETWEVKANAVIMATGGCAFLSKGLGCNVLTGEGLLMSAEAGAELSGMEFTRQYAPSFADGTVTRGRMLAWATLYDEAGRPLHQGDRTFGSIPELMLRGPVYASLDLADTKEKQDFLRNAHPIFFMPLERAGIDPFKDKFPLTLRYEGTMRGTGGLRLTGTDCATSVPGLYAAGDAASREKVTGAISGGGAYNASWAICSGSWAGQGAARHALQEPRPADSRLLRAAGRYGMPAGAGTARALDAKPLIAAVQREILPLRINYFRSEPMVAAALQRLNSLMPELSGQVPATVQGIVQSREAAAMLNVGRWIYTAALARKESRGLQRLAEYPALDPRQTHRLILSGIDTIGIRTESVPHAQELRIPREERAI

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_CP009280_2	2.1\|1307976\|25\|NZ_CP009280\|CRISPRCasFinder	1307976-1308000	25	NZ_CP009280.1	5571069-5571093	0	1.0
NZ_CP009280_2	2.1\|1307976\|25\|NZ_CP009280\|CRISPRCasFinder	1307976-1308000	25	NZ_CP009280.1	1788768-1788792	1	0.96
NZ_CP009280_12	12.1\|4622823\|26\|NZ_CP009280\|CRISPRCasFinder	4622823-4622848	26	NZ_CP009280.1	1232921-1232946	1	0.962
NZ_CP009280_19	19.1\|7050078\|25\|NZ_CP009280\|CRISPRCasFinder	7050078-7050102	25	NZ_CP009280.1	1145029-1145053	1	0.96
NZ_CP009280_2	2.1\|1307976\|25\|NZ_CP009280\|CRISPRCasFinder	1307976-1308000	25	NZ_CP009280.1	5571120-5571144	2	0.92
NZ_CP009280_2	2.1\|1307976\|25\|NZ_CP009280\|CRISPRCasFinder	1307976-1308000	25	NZ_CP009280.1	5571171-5571195	2	0.92
NZ_CP009280_19	19.1\|7050078\|25\|NZ_CP009280\|CRISPRCasFinder	7050078-7050102	25	NZ_CP009280.1	1145080-1145104	2	0.92

1. spacer 2.1|1307976|25|NZ_CP009280|CRISPRCasFinder matches to position: 5571069-5571093, mismatch: 0, identity: 1.0

ttagtgctcttgattccaccggatg	CRISPR spacer
ttagtgctcttgattccaccggatg	Protospacer
*************************

2. spacer 2.1|1307976|25|NZ_CP009280|CRISPRCasFinder matches to position: 1788768-1788792, mismatch: 1, identity: 0.96

ttagtgctcttgattccaccggatg	CRISPR spacer
ttagtgctcttgatttcaccggatg	Protospacer
***************.*********

3. spacer 12.1|4622823|26|NZ_CP009280|CRISPRCasFinder matches to position: 1232921-1232946, mismatch: 1, identity: 0.962

aggcgtatgctttcgaagcgagtttt	CRISPR spacer
aggcgtatgctttcgaagccagtttt	Protospacer
******************* ******

4. spacer 19.1|7050078|25|NZ_CP009280|CRISPRCasFinder matches to position: 1145029-1145053, mismatch: 1, identity: 0.96

ctgcctgccgcccactttcggcaga	CRISPR spacer
ctgcttgccgcccactttcggcaga	Protospacer
****.********************

5. spacer 2.1|1307976|25|NZ_CP009280|CRISPRCasFinder matches to position: 5571120-5571144, mismatch: 2, identity: 0.92

ttagtgctcttgattccaccggatg	CRISPR spacer
ttagtgctcttgatttcatcggatg	Protospacer
***************.**.******

6. spacer 2.1|1307976|25|NZ_CP009280|CRISPRCasFinder matches to position: 5571171-5571195, mismatch: 2, identity: 0.92

ttagtgctcttgattccaccggatg	CRISPR spacer
ttagtgctcttgatttcatcggatg	Protospacer
***************.**.******

7. spacer 19.1|7050078|25|NZ_CP009280|CRISPRCasFinder matches to position: 1145080-1145104, mismatch: 2, identity: 0.92

ctgcctgccgcccactttcggcaga	CRISPR spacer
ctgcttgccgcccactttcggcgga	Protospacer
****.*****************.**

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	MK977711	Streptomyces phage Evy, complete genome	13786-13814	5	0.828
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	KM652554	Streptomyces phage Jay2Jay, complete genome	13976-14004	5	0.828
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	MF358541	Streptomyces phage Warpy, complete genome	13996-14024	5	0.828
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	MT310865	Streptomyces phage Bmoc, complete genome	14193-14221	5	0.828
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	NC_042008	Streptomyces phage Mildred21, complete genome	14118-14146	5	0.828
NZ_CP009280_5	5.2\|2783102\|29\|NZ_CP009280\|CRT	2783102-2783130	29	NC_042010	Streptomyces phage Paradiddles, complete genome	12981-13009	5	0.828
NZ_CP009280_6	6.2\|2783628\|27\|NZ_CP009280\|CRISPRCasFinder	2783628-2783654	27	NC_016972	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG2, complete sequence	58114-58140	6	0.778
NZ_CP009280_20	20.1\|7540920\|27\|NZ_CP009280\|CRISPRCasFinder	7540920-7540946	27	NZ_CP045122	Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence	251362-251388	6	0.778
NZ_CP009280_17	17.1\|5872400\|35\|NZ_CP009280\|CRISPRCasFinder	5872400-5872434	35	NC_015969	UNVERIFIED_ORG: Enterobacter soli plasmid pENTAS02, complete sequence	19704-19738	9	0.743

1. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to MK977711 (Streptomyces phage Evy, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatgctgct	Protospacer
 * ********* **********.***.*

2. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to KM652554 (Streptomyces phage Jay2Jay, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatgctgct	Protospacer
 * ********* **********.***.*

3. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to MF358541 (Streptomyces phage Warpy, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatgctgct	Protospacer
 * ********* **********.***.*

4. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to MT310865 (Streptomyces phage Bmoc, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatcctgct	Protospacer
 * ********* ********** ***.*

5. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to NC_042008 (Streptomyces phage Mildred21, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatcctgct	Protospacer
 * ********* ********** ***.*

6. spacer 5.2|2783102|29|NZ_CP009280|CRT matches to NC_042010 (Streptomyces phage Paradiddles, complete genome) position: , mismatch: 5, identity: 0.828

aagctcaacgtacaacacgccatactgtt	CRISPR spacer
tacctcaacgtagaacacgccatcctgct	Protospacer
 * ********* ********** ***.*

7. spacer 6.2|2783628|27|NZ_CP009280|CRISPRCasFinder matches to NC_016972 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG2, complete sequence) position: , mismatch: 6, identity: 0.778

tgaagctcagatcggctgatcagctta	CRISPR spacer
gtcagcacagaccggctgatcagcttc	Protospacer
   *** ****.**************

8. spacer 20.1|7540920|27|NZ_CP009280|CRISPRCasFinder matches to NZ_CP045122 (Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

atcccgccgctcaacccacttccggcc	CRISPR spacer
cacccgccgcgcaacccgcttccgggg	Protospacer
  ******** ******.*******

9. spacer 17.1|5872400|35|NZ_CP009280|CRISPRCasFinder matches to NC_015969 (UNVERIFIED_ORG: Enterobacter soli plasmid pENTAS02, complete sequence) position: , mismatch: 9, identity: 0.743

gcatgggcaccagcgggaatggcgacagcgacacc	CRISPR spacer
ccaacggcagcagcggcaatggcgacagcggcgga	Protospacer
 **  **** ****** *************.*.

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

181957 : 190978

Streptococcus_phage(28.57%)

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_039302434.1\|181957_183244_+	phosphopyruvate hydratase	W6LP63	Streptococcus_phage	1.2e-170	71.9
WP_042132757.1\|183397_183661_+	hypothetical protein	NA	NA	NA	NA
WP_042132758.1\|183806_184040_+	preprotein translocase subunit SecG	NA	NA	NA	NA
WP_063779817.1\|184273_187285_+	ribonuclease R	Q0GXV6	Lactococcus_phage	1.4e-87	38.9
WP_039296783.1\|187508_187988_+	SsrA-binding protein SmpB	W5RAM5	Staphylococcus_phage	1.7e-40	51.3
WP_042132759.1\|188580_189486_-	hypothetical protein	A0A290FZV2	Caldibacillus_phage	4.9e-12	27.7
WP_042132760.1\|189485_189998_-	recombinase family protein	A0A1P8VVL7	Streptococcus_phage	5.9e-23	38.0
WP_042132761.1\|190077_190548_-	ImmA/IrrE family metallo-endopeptidase	A0A2I7SC21	Paenibacillus_phage	1.3e-29	43.7
WP_063779771.1\|190561_190978_-	helix-turn-helix transcriptional regulator	A0A1Q1PVT4	Staphylococcus_phage	3.6e-18	70.3

DBSCAN-SWA_2

194251 : 213850

Bacillus_phage(26.67%)

capsid,terminase,head,portal,protease,integrase,tail

attL 189732:189746|attR 224422:224436

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
189732:189746	attL	NA	NA	NA	NA
WP_042132768.1\|194251_195604_+	replicative DNA helicase	A0A1P8VVQ6	Streptococcus_phage	1.4e-95	45.4
WP_081969783.1\|195613_196327_+	DUF2786 domain-containing protein	F8WPW8	Bacillus_phage	3.6e-26	32.6
WP_042132769.1\|196366_196567_+	hypothetical protein	NA	NA	NA	NA
WP_042140624.1\|196611_197001_+	ASCH domain-containing protein	A0A2I7QYU6	Vibrio_phage	1.0e-14	43.8
WP_042132771.1\|197259_197469_+	hypothetical protein	NA	NA	NA	NA
WP_042132772.1\|197567_197948_+	hypothetical protein	NA	NA	NA	NA
WP_042140625.1\|198349_198910_+\|integrase	tyrosine-type recombinase/integrase	D2XR58	Bacillus_phage	1.1e-38	45.6
WP_156118500.1\|199194_199899_+	hypothetical protein	NA	NA	NA	NA
WP_042132774.1\|199898_200582_+	HNH endonuclease	A0A1B0YEC6	Lactobacillus_phage	1.9e-08	39.5
WP_042132775.1\|200739_201087_+	hypothetical protein	A0A290GJQ7	Caldibacillus_phage	8.1e-08	33.6
WP_042132776.1\|201043_202768_+\|terminase	terminase large subunit	A0A290GJW3	Caldibacillus_phage	1.9e-73	30.9
WP_081970370.1\|202835_204026_+\|portal	phage portal protein	A0A1L2BY94	Clostridium_phage	3.4e-37	28.3
WP_052421611.1\|204012_204660_+\|head,protease	HK97 family phage prohead protease	A0A0F7L115	uncultured_marine_virus	6.3e-22	39.7
WP_052421612.1\|204670_205960_+\|capsid	phage major capsid protein	NA	NA	NA	NA
WP_042132779.1\|206296_206566_+	hypothetical protein	NA	NA	NA	NA
WP_042132780.1\|206570_206882_+\|head	phage head closure protein	R9TPZ2	Paenibacillus_phage	1.6e-10	42.6
WP_156118501.1\|206883_207315_+	hypothetical protein	A0A0U4J8M6	Bacillus_phage	1.7e-31	50.4
WP_042132782.1\|207317_207695_+	hypothetical protein	NA	NA	NA	NA
WP_042132783.1\|208647_209016_+	hypothetical protein	A0A0U4KKN8	Bacillus_phage	5.2e-13	39.7
WP_081969784.1\|209036_209312_+	hypothetical protein	NA	NA	NA	NA
WP_042132785.1\|209316_211812_+	hypothetical protein	A0A1J1J8L9	Escherichia_phage	2.4e-45	36.9
WP_042132786.1\|211808_212615_+\|tail	phage tail family protein	A0A290FZP5	Caldibacillus_phage	6.8e-50	41.7
WP_042132787.1\|212627_213140_+	hypothetical protein	NA	NA	NA	NA
WP_042132788.1\|213157_213850_+	hypothetical protein	V5Q7N8	Xylella_phage	1.6e-18	51.4
224422:224436	attR	NA	NA	NA	NA

DBSCAN-SWA_3

451622 : 458923

Caulobacter_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042132976.1\|451622_452654_+	agmatine deiminase family protein	M1I5R4	Acanthocystis_turfacea_Chlorella_virus	1.6e-67	38.3
WP_042132978.1\|452814_453690_+	N-carbamoylputrescine amidase	M1GUG4	Paramecium_bursaria_Chlorella_virus	3.0e-75	48.8
WP_081969796.1\|453950_454766_+	transporter substrate-binding domain-containing protein	NA	NA	NA	NA
WP_039299378.1\|454876_455524_+	amino acid ABC transporter permease	NA	NA	NA	NA
WP_042140674.1\|455539_456262_+	amino acid ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	4.9e-23	31.3
WP_042132981.1\|456518_456965_+	tellurite resistance TerB family protein	A0A1Y0T181	Sinorhizobium_phage	1.2e-06	28.6
WP_042132983.1\|457088_457685_+	TerD family protein	K4JRX3	Caulobacter_phage	2.9e-21	32.7
WP_042132985.1\|457714_458290_+	TerD family protein	NA	NA	NA	NA
WP_042132987.1\|458341_458923_+	TerD family protein	K4JRX3	Caulobacter_phage	9.1e-28	37.0

DBSCAN-SWA_4

817629 : 829563

Synechococcus_phage(37.5%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042133396.1\|817629_818925_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	2.0e-22	27.8
WP_042133399.1\|819293_820184_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	7.1e-40	33.1
WP_039298247.1\|820547_820793_+	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	2.2e-07	36.7
WP_039298250.1\|820798_821488_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_042133403.1\|821465_823712_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	1.4e-164	42.7
WP_042140723.1\|823696_825193_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	1.8e-51	32.5
WP_042133407.1\|825884_826925_+	phosphoribosylformylglycinamidine cyclo-ligase	A0A0E3F760	Synechococcus_phage	3.0e-66	45.9
WP_042133409.1\|826924_827539_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	3.4e-25	37.6
WP_042133411.1\|828015_829563_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	1.2e-74	51.0

DBSCAN-SWA_5

2628251 : 2638525

Bacillus_phage(66.67%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042135439.1\|2628251_2630045_+	HAMP domain-containing protein	W8CYF6	Bacillus_phage	2.7e-38	33.1
WP_039304977.1\|2630241_2630970_+	response regulator transcription factor	W8CYM9	Bacillus_phage	1.0e-36	35.2
WP_076242755.1\|2631085_2631865_+	phosphate ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	1.6e-16	33.5
WP_039304983.1\|2631987_2632647_+	phosphate signaling complex protein PhoU	NA	NA	NA	NA
WP_042135442.1\|2632876_2635549_+	DNA polymerase I	A0A1B1IST8	uncultured_Mediterranean_phage	2.6e-45	33.9
WP_042135444.1\|2635600_2636443_+	DNA-formamidopyrimidine glycosylase	A0A127AWE5	Bacillus_phage	2.0e-20	28.4
WP_042135446.1\|2636627_2637356_+	membrane protein	NA	NA	NA	NA
WP_042135448.1\|2637365_2637962_+	dephospho-CoA kinase	NA	NA	NA	NA
WP_042140956.1\|2637961_2638525_+	lytic transglycosylase domain-containing protein	A0A0H3V0Q1	Geobacillus_virus	2.9e-15	37.7

DBSCAN-SWA_6

3438366 : 3454770

Paenibacillus_phage(31.25%)

integrase

attL 3434243:3434255|attR 3451231:3451243

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
3434243:3434255	attL	NA	NA	NA	NA
WP_042136333.1\|3438366_3439518_+\|integrase	site-specific integrase	A0A0U3U8Y8	Bacillus_phage	1.2e-60	41.4
WP_042136339.1\|3439980_3441225_-\|integrase	site-specific integrase	A0A0K2CZ62	Paenibacillus_phage	2.0e-141	60.1
WP_081970495.1\|3441301_3441712_-	ImmA/IrrE family metallo-endopeptidase	Q9T201	Bacillus_phage	7.1e-19	35.1
WP_042136344.1\|3441720_3442131_-	helix-turn-helix transcriptional regulator	Q786F1	Bacillus_phage	5.1e-17	40.6
WP_042136346.1\|3442372_3442630_+	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_042136347.1\|3442616_3442907_+	helix-turn-helix domain-containing protein	A0A2I7SC15	Paenibacillus_phage	2.2e-30	68.4
WP_042136348.1\|3442948_3443155_+	hypothetical protein	NA	NA	NA	NA
WP_042136349.1\|3443170_3444304_+	plasmid partitioning protein	A0A1D6Z271	Staphylococcus_phage	1.3e-38	45.7
WP_042136350.1\|3444290_3444734_+	ABC transporter permease	A0A220GJF4	Streptococcus_phage	8.2e-05	24.5
WP_042136352.1\|3445005_3446070_+	replication protein	S5M5Q5	Brevibacillus_phage	3.2e-47	33.9
WP_042136354.1\|3446070_3447051_+	AAA family ATPase	S5MU12	Brevibacillus_phage	2.3e-60	44.2
WP_042136356.1\|3447053_3448157_+	DNA polymerase III subunit beta	D0R7I4	Paenibacillus_phage	1.8e-21	34.7
WP_042136358.1\|3448159_3448705_+	hypothetical protein	NA	NA	NA	NA
WP_156118608.1\|3448760_3448934_+	hypothetical protein	NA	NA	NA	NA
WP_063779798.1\|3448900_3450853_+	DNA methyltransferase	L7TH64	Pseudomonas_virus	5.7e-82	35.1
WP_144025995.1\|3450879_3451095_-	helix-turn-helix domain-containing protein	A0A288WG81	Bacillus_phage	1.7e-11	55.0
WP_156118609.1\|3451253_3451427_+	hypothetical protein	NA	NA	NA	NA
3451231:3451243	attR	NA	NA	NA	NA
WP_042136366.1\|3451499_3452177_+	hypothetical protein	D0R7I8	Paenibacillus_phage	1.4e-59	61.2
WP_042136368.1\|3452191_3452785_+	sigma-70 family RNA polymerase sigma factor	A0A2I7SC33	Paenibacillus_phage	3.4e-14	26.8
WP_052421831.1\|3452859_3454035_+	hypothetical protein	Q8W6F2	Sinorhizobium_phage	1.1e-16	31.4
WP_042136370.1\|3454299_3454770_+	ASCH domain-containing protein	A0A068CCC0	Rhizobium_phage	1.3e-08	31.5

DBSCAN-SWA_7

5341004 : 5349182

Staphylococcus_phage(57.14%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042138651.1\|5341004_5342243_-	D-alanyl-D-alanine carboxypeptidase	A0A1P8VVG5	Erythrobacter_phage	2.2e-07	33.3
WP_039301696.1\|5342419_5342908_-	sporulation protein YtfJ	NA	NA	NA	NA
WP_042138652.1\|5342990_5343686_-	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_039301691.1\|5343867_5344470_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	4.1e-15	33.0
WP_042138653.1\|5344438_5345230_-	segregation and condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	1.9e-07	36.2
WP_036727378.1\|5345466_5345934_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	9.5e-44	58.3
WP_042138654.1\|5345976_5347230_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	1.0e-116	53.9
WP_042138655.1\|5347290_5347959_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	1.1e-37	38.9
WP_042138656.1\|5348084_5349182_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	7.4e-55	37.1

DBSCAN-SWA_8

6387638 : 6430405

Bacillus_phage(24.0%)

capsid,plate,terminase,head,portal,protease,integrase,holin

attL 6401762:6401775|attR 6431458:6431471

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042139300.1\|6387638_6388850_+\|integrase	site-specific integrase	A0A2I7SC08	Paenibacillus_phage	5.9e-29	30.5
WP_052422035.1\|6389254_6389710_-	hypothetical protein	NA	NA	NA	NA
WP_042139301.1\|6389786_6390473_-	hypothetical protein	A0A127AWA8	Bacillus_phage	5.1e-46	63.8
WP_042139302.1\|6390922_6391258_-	hypothetical protein	NA	NA	NA	NA
WP_144026073.1\|6391502_6392123_-	hypothetical protein	NA	NA	NA	NA
WP_052422036.1\|6392321_6392819_+	PH domain-containing protein	NA	NA	NA	NA
WP_052422201.1\|6392834_6394310_-	glycosyl hydrolase	NA	NA	NA	NA
WP_042139305.1\|6394537_6394978_+	DNA-entry nuclease	F8WPS9	Bacillus_phage	8.4e-34	62.6
WP_156118708.1\|6395217_6395355_+	hypothetical protein	NA	NA	NA	NA
WP_155991357.1\|6395403_6395559_-	hypothetical protein	NA	NA	NA	NA
WP_076243860.1\|6395728_6395905_+	putative motility protein	NA	NA	NA	NA
WP_042139306.1\|6396048_6396591_+	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_156118709.1\|6396678_6396843_+	hypothetical protein	NA	NA	NA	NA
WP_156118710.1\|6397185_6397344_+	hypothetical protein	NA	NA	NA	NA
WP_042139308.1\|6397340_6397538_-	hypothetical protein	NA	NA	NA	NA
WP_156118711.1\|6397676_6398414_+	hypothetical protein	NA	NA	NA	NA
WP_156118712.1\|6398367_6398631_-	hypothetical protein	NA	NA	NA	NA
WP_042139311.1\|6398718_6398988_-	hypothetical protein	NA	NA	NA	NA
WP_042139312.1\|6399089_6399449_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_042139313.1\|6400332_6400722_-	hypothetical protein	NA	NA	NA	NA
WP_042139314.1\|6400902_6401706_-	undecaprenyl-diphosphate phosphatase	NA	NA	NA	NA
6401762:6401775	attL	NA	NA	NA	NA
WP_042139315.1\|6402509_6402926_+	extradiol dioxygenase	NA	NA	NA	NA
WP_042139317.1\|6403683_6404346_-	hypothetical protein	NA	NA	NA	NA
WP_081970159.1\|6404350_6405580_-	ATP-binding protein	NA	NA	NA	NA
WP_042139318.1\|6405676_6406072_-	hypothetical protein	NA	NA	NA	NA
WP_156118713.1\|6406152_6406386_-	hypothetical protein	NA	NA	NA	NA
WP_042139321.1\|6406657_6406867_-	hypothetical protein	NA	NA	NA	NA
WP_052422037.1\|6406869_6407715_-	M15 family metallopeptidase	A0A0A0RV08	Bacillus_phage	2.1e-41	54.7
WP_081970161.1\|6407720_6408230_-\|holin	phage holin family protein	D9ZNF2	Clostridium_phage	9.7e-18	38.4
WP_042139323.1\|6408465_6408852_-	hypothetical protein	S6C455	Thermus_phage	2.9e-30	58.2
WP_052422038.1\|6408871_6410629_-	hypothetical protein	S6B1J7	Thermus_phage	8.0e-27	27.3
WP_042139324.1\|6410639_6411251_-	YmfQ family protein	S6BFJ0	Thermus_phage	1.5e-49	56.3
WP_081970163.1\|6411254_6411596_-	hypothetical protein	NA	NA	NA	NA
WP_042139325.1\|6411608_6412631_-	DUF2793 domain-containing protein	A0A0K1Y6G9	Rhodobacter_phage	1.9e-12	36.8
WP_042139326.1\|6412632_6413046_-	hypothetical protein	A0A0A7S1G0	Clostridium_phage	1.4e-35	59.7
WP_081970165.1\|6413049_6414183_-\|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	6.2e-49	40.3
WP_042139327.1\|6414139_6414502_-	DUF2634 domain-containing protein	E5DV62	Deep-sea_thermophilic_phage	7.9e-14	37.5
WP_042139329.1\|6414489_6414903_-	hypothetical protein	NA	NA	NA	NA
WP_052422040.1\|6414899_6415694_-	hypothetical protein	A0A1L2JY62	Aeribacillus_phage	9.1e-55	40.7
WP_042139330.1\|6415686_6416007_-	hypothetical protein	E5DV60	Deep-sea_thermophilic_phage	1.7e-15	42.9
WP_042139331.1\|6416006_6416531_-	hypothetical protein	A8ATH7	Listeria_phage	9.4e-08	33.6
WP_042139332.1\|6416517_6419046_-	hypothetical protein	A0A1L2BYA6	Clostridium_phage	4.0e-19	39.6
WP_156118714.1\|6419093_6419288_-	hypothetical protein	NA	NA	NA	NA
WP_042139334.1\|6419271_6419568_-	hypothetical protein	NA	NA	NA	NA
WP_052422041.1\|6419597_6419996_-	DUF3277 family protein	A0A1L2K2P1	Aeribacillus_phage	9.3e-24	46.5
WP_042139335.1\|6420008_6421034_-	DUF3383 family protein	A0A1L2JZ70	Aeribacillus_phage	2.1e-67	44.1
WP_042139337.1\|6421020_6421518_-	hypothetical protein	NA	NA	NA	NA
WP_042139338.1\|6421504_6421849_-	hypothetical protein	NA	NA	NA	NA
WP_042139339.1\|6421851_6422328_-	hypothetical protein	NA	NA	NA	NA
WP_042139340.1\|6422337_6422886_-	hypothetical protein	NA	NA	NA	NA
WP_042139341.1\|6422860_6423130_-	hypothetical protein	NA	NA	NA	NA
WP_042139342.1\|6423189_6424389_-\|capsid	phage major capsid protein	A0A2I7SBY4	Paenibacillus_phage	2.9e-105	58.0
WP_042139343.1\|6424438_6425032_-\|head,protease	HK97 family phage prohead protease	A0A2I7SBY1	Paenibacillus_phage	2.7e-59	61.2
WP_042139344.1\|6424976_6426350_-\|portal	phage portal protein	Q2I8F9	Bacillus_phage	1.9e-153	63.5
WP_042139345.1\|6426399_6427992_-\|terminase	terminase large subunit	A0A2I7SBY8	Paenibacillus_phage	2.2e-289	87.7
WP_042139346.1\|6427981_6428596_-\|terminase	terminase	A0A2I7SBY3	Paenibacillus_phage	1.7e-80	74.8
WP_042139347.1\|6428768_6429131_-	HNH endonuclease	Q38456	Bacillus_phage	4.2e-31	54.4
WP_042139348.1\|6429114_6429567_-	hypothetical protein	NA	NA	NA	NA
WP_042139349.1\|6429847_6430405_-\|integrase	site-specific integrase	H0USV4	Bacillus_phage	1.2e-50	56.3
6431458:6431471	attR	NA	NA	NA	NA

DBSCAN-SWA_9

7622869 : 7640059

Clostridium_phage(35.0%)

plate,portal,tail,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042140102.1\|7622869_7623151_-\|holin	holin	A0A2H4JD26	uncultured_Caudovirales_phage	5.5e-07	41.4
WP_042140103.1\|7623147_7623858_-	hypothetical protein	A0A127AWA8	Bacillus_phage	6.7e-41	54.4
WP_042140104.1\|7623829_7624222_-	hypothetical protein	NA	NA	NA	NA
WP_042140105.1\|7624208_7624406_-	hypothetical protein	NA	NA	NA	NA
WP_039294205.1\|7624407_7624722_-	hypothetical protein	NA	NA	NA	NA
WP_052422122.1\|7624963_7625356_-	hypothetical protein	S6C455	Thermus_phage	2.7e-28	52.3
WP_042140107.1\|7625365_7627072_-	hypothetical protein	S6B1J7	Thermus_phage	1.0e-39	31.1
WP_042140108.1\|7627083_7627695_-	YmfQ family protein	S6BFJ0	Thermus_phage	1.6e-46	52.6
WP_081970300.1\|7627697_7628033_-	hypothetical protein	A0A0A7S181	Clostridium_phage	2.5e-06	68.6
WP_042140109.1\|7628045_7629068_-	DUF2793 domain-containing protein	A0A0K1LM54	Rhodobacter_phage	7.2e-12	36.8
WP_042140110.1\|7629069_7629483_-	hypothetical protein	A0A0A7RW10	Clostridium_phage	3.4e-29	49.2
WP_042140111.1\|7629485_7630544_-\|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	2.1e-91	52.6
WP_052422123.1\|7630536_7630965_-	DUF2634 domain-containing protein	A0A0A7RTU4	Clostridium_phage	4.6e-21	42.1
WP_042140112.1\|7630961_7631255_-	DUF2577 domain-containing protein	A0A0A7RTJ2	Clostridium_phage	4.1e-13	37.5
WP_042140113.1\|7631260_7632223_-	hypothetical protein	S5MNC9	Brevibacillus_phage	4.2e-86	47.2
WP_042140114.1\|7632235_7632982_-	LysM peptidoglycan-binding domain-containing protein	A0A0K2CNM3	Brevibacillus_phage	4.0e-44	43.3
WP_042140115.1\|7632983_7634816_-	hypothetical protein	S5MNW9	Brevibacillus_phage	1.3e-40	33.3
WP_076247148.1\|7634829_7635009_-	hypothetical protein	NA	NA	NA	NA
WP_039294170.1\|7635008_7635431_-\|portal	phage portal protein	A0A0A7RTY8	Clostridium_phage	2.3e-12	38.9
WP_039294168.1\|7635538_7636009_-\|tail	phage tail tube protein	A0A0A7RVP1	Clostridium_phage	7.5e-49	60.9
WP_042140116.1\|7636010_7637333_-	phage-like element PBSX protein XkdK	A0A0A7RTT5	Clostridium_phage	1.0e-111	49.4
WP_042140117.1\|7637332_7637539_-	hypothetical protein	NA	NA	NA	NA
WP_042140118.1\|7637535_7637958_-	hypothetical protein	NA	NA	NA	NA
WP_144026172.1\|7638382_7638862_-	transcriptional regulator	A0A0C5AN03	Paenibacillus_phage	9.4e-39	61.9
WP_042140119.1\|7639157_7639601_+	helix-turn-helix domain-containing protein	S6C481	Thermus_phage	9.0e-20	42.7
WP_039294354.1\|7639645_7640059_+	ImmA/IrrE family metallo-endopeptidase	Q9T201	Bacillus_phage	4.6e-18	38.2

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_CP009280

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

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