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_CP029192	Streptomyces venezuelae strain ATCC 14584 chromosome, complete genome	17 crisprs	WYL,csa3,DEDDh,DinG,PD-DExK,cas3,RT,Cas9_archaeal,cas4,casR	3	10	0	0

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP029192_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_1

2683550-2683824

Orphan

Consensus_repeat	Method
GGNCTTCTTGGCGGTGGCCTTCTTCGCCG	CRT

4 spacers

The CRISPR arrays of NZ_CP029192_1

>merge|NZ_CP029192|1|2683550-2683824|CRT
CGCCTTCTTGGCGGTGGCCTTCTTCGCCGGGGCGGTCTTCTTGGCCGTGGCCTTCTTCGCCGCCGGGGTGGCCTTCTTGGCGGTGGTCTTCTTCGCCGCCGGGGTCGCCTTCTTGGCCGTGGCCTTGGTGGCGGTCTTCTTGGCGGTGGCCTTCTTCGCCGCTGCCTTCTTCGCCGTCGCCGTGGTCTTCTTGGCGGTGGCGGTGGTCTTCTTGGCCGTGGTCTTCTTCGCCGTGGCCTTCGTGGCGGTCTTCTTGGCGGTGGCCTTCTTCGCCG

>NZ_CP029192|1|1|2683550-2683824|CRT
CGCCTTCTTGGCGGTGGCCTTCTTCGCCG	GGGCGGTCTTCTTGGCCGTGGCCTTCTTCGCCGCCGGGGT
GGCCTTCTTGGCGGTGGTCTTCTTCGCCG	CCGGGGTCGCCTTCTTGGCCGTGGCCTTGGTGGC
GGTCTTCTTGGCGGTGGCCTTCTTCGCCG	CTGCCTTCTTCGCCGTCGCCGT
GGTCTTCTTGGCGGTGGCGGTGGTCTTCT	TGGCCGTGGTCTTCTTCGCCGTGGCCTTCGTGGC
GGTCTTCTTGGCGGTGGCCTTCTTCGCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150215989.1\|2674436_2676113_-\|DAK2-domain-containing-protein	unknown	unknown	gnl\|CDD\|274671
NZ_CP029192.1\|WP_150221113.1\|2687859_2688318_-\|DUF4188-domain-containing-protein	unknown	unknown	gnl\|CDD\|316352
NZ_CP029192.1\|WP_150215991.1\|2677412_2678381_-\|thiamine-phosphate-kinase	unknown	unknown	gnl\|CDD\|235583
NZ_CP029192.1\|WP_055564460.1\|2687024_2687744_+\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP029192.1\|WP_016642988.1\|2678593_2678827_+\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366431
NZ_CP029192.1\|WP_150215996.1\|2685419_2686844_-\|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl\|CDD\|235490
NZ_CP029192.1\|WP_150215993.1\|2681596_2682376_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP029192.1\|WP_150215999.1\|2690697_2692176_-\|glutamate--tRNA-ligase	unknown	unknown	gnl\|CDD\|234953
NZ_CP029192.1\|WP_055564463.1\|2684346_2684583_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150215988.1\|2672173_2674375_-\|ATP-dependent-DNA-helicase-RecG	unknown	unknown	gnl\|CDD\|236794
NZ_CP029192.1\|WP_150215990.1\|2676627_2677416_-\|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	unknown	unknown	gnl\|CDD\|180561
NZ_CP029192.1\|WP_150215995.1\|2684820_2685414_-\|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl\|CDD\|179314
NZ_CP029192.1\|WP_150216000.1\|2692168_2692957_-\|DUF2437-domain-containing-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP029192.1\|WP_016642993.1\|2676352_2676538_+\|50S-ribosomal-protein-L28	unknown	unknown	gnl\|CDD\|234736
NZ_CP029192.1\|WP_150221111.1\|2678886_2679345_+\|DUF3515-family-protein	unknown	unknown	gnl\|CDD\|378794
NZ_CP029192.1\|WP_150216001.1\|2693036_2693237_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150215992.1\|2679368_2680526_-\|D-alanine--D-alanine-ligase	unknown	unknown	gnl\|CDD\|234993
NZ_CP029192.1\|WP_150215997.1\|2688409_2689108_+\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133407
NZ_CP029192.1\|WP_150221112.1\|2680571_2681588_-\|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|234629
NZ_CP029192.1\|WP_150215998.1\|2689781_2690510_-\|HAD-IA-family-hydrolase	unknown	unknown	gnl\|CDD\|223943

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150215989.1\|2674436_2676113_-\|DAK2-domain-containing-protein	gnl\|CDD\|274671	TIGR03599, YloV, DAK2 domain fusion protein YloV. This model describes a protein family that contains an N-terminal DAK2 domain (pfam02734), so named because of similarity to the dihydroxyacetone kinase family family. The GTP-binding protein CgtA (a member of the obg family) is a bacterial GTPase associated with ribosome biogenesis, and it has a characteristic extension (TIGR03595) in certain lineages. This protein family described here was found, by the method of partial phylognetic profiling, to have a phylogenetic distribution strongly correlated to that of TIGR03595. This correlation implies some form of functional coupling.	4.83978e-145
NZ_CP029192.1\|WP_150221113.1\|2687859_2688318_-\|DUF4188-domain-containing-protein	gnl\|CDD\|316352	pfam13826, DUF4188, Domain of unknown function (DUF4188).	1.13546e-54
NZ_CP029192.1\|WP_150215991.1\|2677412_2678381_-\|thiamine-phosphate-kinase	gnl\|CDD\|235583	PRK05731, PRK05731, thiamine monophosphate kinase; Provisional.	1.58228e-130
NZ_CP029192.1\|WP_055564460.1\|2687024_2687744_+\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	7.69317e-46
NZ_CP029192.1\|WP_016642988.1\|2678593_2678827_+\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|366431	pfam01037, AsnC_trans_reg, Lrp/AsnC ligand binding domain. The l-leucine-responsive regulatory protein (Lrp/AsnC) family is a family of similar bacterial transcription regulatory proteins. The family is named after two E. coli proteins involved in regulating amino acid metabolism. This entry corresponds to the usually C-terminal regulatory ligand binding domain. Structurally this domain has a dimeric alpha/beta barrel fold.	1.3259e-08
NZ_CP029192.1\|WP_150215996.1\|2685419_2686844_-\|3-isopropylmalate-dehydratase-large-subunit	gnl\|CDD\|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_CP029192.1\|WP_150215993.1\|2681596_2682376_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	5.05273e-42
NZ_CP029192.1\|WP_150215999.1\|2690697_2692176_-\|glutamate--tRNA-ligase	gnl\|CDD\|234953	PRK01406, gltX, glutamyl-tRNA synthetase; Reviewed.	0
NZ_CP029192.1\|WP_150215995.1\|2684820_2685414_-\|3-isopropylmalate-dehydratase-small-subunit	gnl\|CDD\|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	1.59871e-122
NZ_CP029192.1\|WP_150215988.1\|2672173_2674375_-\|ATP-dependent-DNA-helicase-RecG	gnl\|CDD\|236794	PRK10917, PRK10917, ATP-dependent DNA helicase RecG; Provisional.	0
NZ_CP029192.1\|WP_150215990.1\|2676627_2677416_-\|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	gnl\|CDD\|180561	PRK06427, PRK06427, bifunctional hydroxy-methylpyrimidine kinase/ hydroxy-phosphomethylpyrimidine kinase; Reviewed.	1.75755e-125
NZ_CP029192.1\|WP_150216000.1\|2692168_2692957_-\|DUF2437-domain-containing-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].	9.20942e-98
NZ_CP029192.1\|WP_016642993.1\|2676352_2676538_+\|50S-ribosomal-protein-L28	gnl\|CDD\|234736	PRK00359, rpmB, 50S ribosomal protein L28; Reviewed.	6.10405e-24
NZ_CP029192.1\|WP_150221111.1\|2678886_2679345_+\|DUF3515-family-protein	gnl\|CDD\|378794	pfam12028, DUF3515, Protein of unknown function (DUF3515). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 166 to 214 amino acids in length. This protein has a conserved RCG sequence motif.	2.87392e-21
NZ_CP029192.1\|WP_150215992.1\|2679368_2680526_-\|D-alanine--D-alanine-ligase	gnl\|CDD\|234993	PRK01966, ddl, D-alanine--D-alanine ligase.	8.25292e-175
NZ_CP029192.1\|WP_150215997.1\|2688409_2689108_+\|MerR-family-transcriptional-regulator	gnl\|CDD\|133407	cd04780, HTH_MerR-like_sg5, Helix-Turn-Helix DNA binding domain of putative transcription regulators from the MerR superfamily. Putative helix-turn-helix (HTH) MerR-like transcription regulators (subgroup 5), N-terminal domain. Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	6.09705e-30
NZ_CP029192.1\|WP_150221112.1\|2680571_2681588_-\|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase	gnl\|CDD\|234629	PRK00094, gpsA, NAD(P)H-dependent glycerol-3-phosphate dehydrogenase.	0
NZ_CP029192.1\|WP_150215998.1\|2689781_2690510_-\|HAD-IA-family-hydrolase	gnl\|CDD\|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	2.41725e-36

>NZ_CP029192.1|WP_150215993.1|2681596_2682376_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSRRRIGFWYRLAAVIAKPPLVVLFKRDWRGMEHIPADGGFITAVNHNSHIDPFSYAHYQYNTGRVPRFLAKDGLFKGGFVAKVMKGTGQIPVYRETTNALDAFRAAVDAIERGECVAFYPEGTLTRDPDMWPMTAKSGAARVALKTKCPVIPVAQWGANLALPPYSKKPAFFPRKTLQVKAGAPVDLSRFYDKEPTPDVLREVTETIMAAITELLEEVRGEKAPDTPYDPRRARLEQRRKADRGTARGSAESTSEDSK
>NZ_CP029192.1|WP_150221112.1|2680571_2681588_-|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase
MNSARPVKAAVFGTGSWGTAFGMVLADAGCDVTLWGRRTELADAVNSTRTNPDYLPGVRLPENLRATSDPAEAAADADFTVLAVPSQTLRGNLAEWAPLLAPETVLVSLMKGVELGSAMRMSEVIEDVTKVPSDRVAVVTGPNLAREIAARQPAAAVVACRDEAVAQRLQTACHTPYFRPYTNTDVVGCELGGAVKNVIGLAVGIADGMGLGDNAKGSLITRGLAETTRLGLAMGADPLTFSGLAGLGDLVATCSSPLSRNHTFGTNLGKGMTLEETIAVTKQTAEGVKSCESVLDLARRHGVDMPITETVVGIVHEGTPPMVALKDLMSRSAKPERR
>NZ_CP029192.1|WP_150215992.1|2679368_2680526_-|D-alanine--D-alanine-ligase
MSSENLPQSPEQPLRKPRVAVVFGGRSSEHGISVVTAGAVLRAIDRTKYDVLPIGITTDGRWALTADEPERMAIADRTMPNVSDLADSVEGGVVLPLDPGNREVVYSEPGSVPKALGEVDVVFPMLHGPYGEDGTLQGLLELSGVPYVGSGVLASAVGQDKDYMKRVFSSFGLNVGPYLVIRPREWQQDEEGARRRIADFAGEHGFPLFIKPARAGSSIGITKVDSFEGLDEAIAEAQHHDPKILVEALLRGREIECGVLEFEDGPRASVPAEIPPVQAHDYYDFEAKYIDSAPGIVPAPLTPDETAEIQRLAVEAFEAASCEGLVRADFFLTEDGRFVINEINTMPGFTPISMYPQMWEKSGVSYPELVDRLIQAALNRSTGLR
>NZ_CP029192.1|WP_150221111.1|2678886_2679345_+|DUF3515-family-protein
MSALALSITTAACSGTDDEASVVVPSPDAKAASLCRDLHEQLPEKVDGLGRTDPGPKSDLTAGWGDPAIILRCGVPRPPKMIDLSYAPKNGVKVNGVAWLLEKRDDGSYTFTTGARLAYVEVTLPKERTGGGLGPLTDFAAPIKKTVPKGIA
>NZ_CP029192.1|WP_016642988.1|2678593_2678827_+|Lrp/AsnC-family-transcriptional-regulator
MVQAYILIQTEVGKASTVAELIGKIPGVIQAEDVTGPYDVIVRAQADTVDELGRMVVAKVQQVDGITRTLTCPVVHL
>NZ_CP029192.1|WP_150215991.1|2677412_2678381_-|thiamine-phosphate-kinase
MKGSVGELGEFGLIRELTSRLTSTPAVRLGPGDDAAVVTAPDRRVVASTDILLEGRHFRRDWSTAYDVGRKAAAQNLADIAAMGAVPTALLLGLVVPAELPASWPTELMDGLRDECQVAGAAVVGGDVVRGDTITVAITALGDLRNHEPVTRAGAQTGDVVAVTGWLGWSAAGHAVLSRGFRSPRAFVEAHRRPEPPYHAGPAAAGLGATSMTDVSDGLIADLGHIAEASKVRIDIRSGDVDVPSQMNDIGQAVGVDPLQWVLNGGEDHAIVATFPPDVKLPARWKVIGEVLNPSALPQVTVDGAPWTSKGWDHFGDNGDTE
>NZ_CP029192.1|WP_150215990.1|2676627_2677416_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase
MTAPPRVLTVAGSDSGGGAGIQADLKTMLALGTHGMSVVTAVTAQNSLGVQGFWELPVEAVRAQYRSVVDDIGVQAVKTGMLASAALVETVAELIAGTDAPAVVDPVGVSKHGDSLLAASALDSVRTKLLPAATVATPNLDEVAQLTGVEVDSEDGLRRAADAVLAYGPKWVLIKGGHLRGDAVDLLTDGSEEHVLRAPRHDNRHTHGTGCTLASAIASQLAKGQGVPEAVAAAKEYVTGAIAEGFALGGGIGPVDHGWRSK
>NZ_CP029192.1|WP_016642993.1|2676352_2676538_+|50S-ribosomal-protein-L28
MAANCDVCGKGPGFGNNISHSHRRTPRRWNPNIQRVRAVVSGTPKRLNACTSCIKAGKVSR
>NZ_CP029192.1|WP_150215989.1|2674436_2676113_-|DAK2-domain-containing-protein
MPQNLDAVAVRAWCRLALDALGRAREEIDSINVYPVADGDTGTNLYLTVESASQAVDAAFTGHEPALPSLTETVRAMAHGALIGARGNSGTILSQLLRGMAQVIGADGVPRGEADHVEGPVLERALRQAAESAYQAVAHPVEGTVLTVATAAADAATGTGGDCGAVARAAYEGARAALEATPGQLAVLGRAGVVDAGGRGLVAVLGALTGALSGEPLTARGAAHGKGSVHGHARVEAVECEDVPGDESGPAFEVIYLLEADDAAVTRLRARLDRLGDSLVVVGGDGLWNVHVHVDDAGAAVEAGVEAGRPHRIRITHFGADDAHTTTPHTTAQPPRERAQRAVVAVVPGEGLAGLYAEAGATTVPTRVGEPPASGELVDAIRRAHAREVVLLPNDAELRHTAAAAAEQARTEGVRVALIPTRSAVQGIAALAVHEPDRRFDEDVVAMTSAAGATRYGELAVAERQSWTMAGICQTGDVLGLIDGDVAVIGAEVARTAVSVLDRMLSAGGEMVTLVLGESVPDTVAEHLEKHVREAYLAVDTVVYRGGRQSALMLIGVE
>NZ_CP029192.1|WP_150215988.1|2672173_2674375_-|ATP-dependent-DNA-helicase-RecG
MDLVPALEEPLKKVVGPATAKVMAEHLDLHTVGDLLHHYPRRYAERGELTRLADLPLDEHVTVVAQVATARILKFNGGRGQRLEVTITDGSGQVQLVFFGRGIHKPHKDLLPGTRAMFAGKVSVFNRKMQLAHPAYELLRGDGDEAGETVGSWAGAQLPIYPATAKLESWKIAKSVDMVLPSAQEAQDPLPPSLRDGRGLIPLPEALLKIHRPHSKADIAAARDRLKWDEAFVLQVALARRRYADAQLPAVARRRKPGGLLDAFDAKLPFTLTDGQEKVSKEIFDDLATEHPMHRLLQGEVGSGKTMVALRAMLAVVDAGGQAAMLAPTEVLAQQHHRSIVEMMGELAEGGMLGGAEHATKVTLLTGSMGAASRRQALLDLVTGDAGIVIGTHALIEDKVQFHDLGLVVVDEQHRFGVEQRDALRGKGKQPPHLLVMTATPIPRTVAMTVFGDLETSVLDQLPAGRSPIASHVVPAEDKPHFLARAWERVREEVENGHQAYVVCPRIGDEEEDPKKAKKKAEEEATAEKRPPLAVVEVAEQLARGPLSGLKVEVLHGRMQPDDKDAVMRRFAAGETQVLVATTVIEVGVNVPNATAMVIMDADRFGVSQLHQLRGRVGRGSAPGLCLLVTDMPEASPARGRLGAVASTLDGFELSRIDLEQRREGDVLGQAQSGVRSSLRMLAVIDDEEIIAAAREEAVAVVADDPELERLPALRTALDALLDAEREQYLDKG
>NZ_CP029192.1|WP_055564463.1|2684346_2684583_-|hypothetical-protein
MGRDSQLELYGLVADQLKEAHSRVRALQVPEGVRMALTRKLLVITAAAKHDLADAARRLERLMASLDEADEGRFPQDG
>NZ_CP029192.1|WP_150215995.1|2684820_2685414_-|3-isopropylmalate-dehydratase-small-subunit
MEAFTKHTGRAVPLRRSNVDTDQIIPAHWLKKVTRDGFEDGLFEAWRKDSEFVLNRPERQGSTVLVAGPDFGTGSSREHAVWALQNFGFKAVISSRFADIFRGNSLKNGLLTVVLDQKVVDALWELTERDPQAEITVDLEDRQVRAEGITADFELDENARWRLLNGLDDISITLQNEPDIAAYESGRPSYKPRTVQV
>NZ_CP029192.1|WP_150215996.1|2685419_2686844_-|3-isopropylmalate-dehydratase-large-subunit
MGRTLAEKVWDDHVVRRAEGEPDLLFIDLHLLHEVTSPQAFDGLRQAGRPVRRLDLTIATEDHNTPTLDIDKPIADPVSRAQLETLRKNCAEFGVRLHPLGDVEQGVVHVVGPQLGLTQPGTTVVCGDSHTSTHGAFGALAFGIGTSQVEHVLATQTLPMARPKTMAITVDGELPDGVTAKDLILAIIAKIGTGGGQGYVLEYRGSAVEKLSMEARMTICNMSIEAGARAGMIAPDQTTFDYIEGRAHAPRGEDWDAAVAYWKTLKTDDDAVFDAEVYIDAASLAPFVTWGTNPGQGAPLSASVPDPASYEDASERYAAEKALEYMGLTAGQPLRDIKVDTVFVGSCTNGRIEDLRAAASIVEGRKVADGVRMLVVPGSVRVALQAVEEGLDKVFTGAGAEWRHAGCSMCLGMNPDQLAPGERSASTSNRNFEGRQGKGGRTHLVSPQVAAATAVTGHLASPADLSDAPVTAGV
>NZ_CP029192.1|WP_055564460.1|2687024_2687744_+|IclR-family-transcriptional-regulator
MDNSSGVGVLDKAALVLSALESGPATLAGLVAATGLARPTAHRLAVALEHHRMVARDMQGRFILGPRLSELAAAAGEDRLLATAGPVLTHLRDVTGESAQLYRRQGDMRICVAAAERLSGLRDTVPVGSTLTMKAGSSAQILMAWEEPERLHRGLQGARFTATALSGVRRRGWAQSIGEREPGVASVSAPVRGPSNRVVAAVSVSGPIERLTRHPGRMHAQAVIDAAGRLSEALRRSGG
>NZ_CP029192.1|WP_150221113.1|2687859_2688318_-|DUF4188-domain-containing-protein
MTAEAEGDVVVFHIGMRINAFRAVRSWWPVFRAMPRMLKELSRDRESGMLGYRLLFGGTRVVYVVQYWESQEKLLAYSTAQDKAHRPAWAAFNRRIREGRGKVGFWHETFVVPAGAHEQVYVNMPPFGLGAATGVIPVGRRGERAADRLTAV
>NZ_CP029192.1|WP_150215997.1|2688409_2689108_+|MerR-family-transcriptional-regulator
MALSKEERKRRHEPMRLAELSRRSGVPTATIKYYLREGLLPPGHRVTATQAEYDDAHLQRLRLVRALVQVGRVPIASAREVLTALEDDSLDHNSRLGTAVWALPHGPESAAADPAEDAARHTVDALLERLGWRNAQGYGAKSPAYRMLVTAVGTLARLGYPCDVADLAPYARAGRQLADADLDLIERYESPDEQLEAAVALTVLYEPVLLSLRRMAQAEESNRRYGQKEPRE
>NZ_CP029192.1|WP_150215998.1|2689781_2690510_-|HAD-IA-family-hydrolase
MPIKAVVWDIDDTIFDYARADSTGMHAHLTAEGLLERYESAERALDRWRELTERHWARFGAGGVTFQEQRRDRVRDFMDAPALSDDDADAWFERYVGHYESAWSLFPDTLPTLDELAGEYRHAVLSNSALVVQDRKLTVLGVRDRFEAVLCAADLGVSKPAAEAFLAVCAHLGLAPAEIAYVGDQPEIDARGARDAGLLGIWLDRNGSTGDGPTGVHRIRALSELPALLRADTRFGAPSTFG
>NZ_CP029192.1|WP_150215999.1|2690697_2692176_-|glutamate--tRNA-ligase
MANATPVRVRFCPSPTGNPHVGLVRTALFNWAYARHNEGTLVFRIEDTDAARDSEESYEQLLDSMRWLGFDWDEGPEVGGPHAPYRQSQRMEIYKDVAAKLIDGGYAYPCYCTTEELDARREAARAAGKPSGYDGHCRDLTAEQIQAYEAEGRKHIIRFRMPDEATTFTDLVRGEITVQAENVTDYGIVRANGAPLYTLVNPVDDALMEITHVLRGEDLLSSTPRQIALYKALIELGIAKAIPEFGHLPYVMGEGNKKLSKRDPQASLNLYRERGFLPEGLLNYLSLLGWSFSADQDVFSIPDMVAKFDLADVNANPARFDLKKAEAINADHIRMLDVKTFAEACEPWLKAPHANWAPEEFDEAAWQAIAPHAQTRLKVLSEITDNVDFLFRAEPVFDEPSWTKAMKEGSDALLRTARAKLDAADWTSPESLKEAVLAAGEEHGLKLGKAQAPVRVAVTGRTIGLPLFESLEILGKEKALTRIDAALAKLTA
>NZ_CP029192.1|WP_150216000.1|2692168_2692957_-|DUF2437-domain-containing-protein
MRIARFSIDGNVAFGAVEGESPPGTTDGLVLDIIKGIPFADFELSGTKVPLSKVRLLPPVLPNKVVAIGRNYAEHAAELGNEVPDIPVAFFKPSTSVAGPGDAIVYPSFSQEVHHEAELAVVIGRMCREVPRERARDVILGYTCANDVTARDVQKRENQWARAKGFDTSCPLGPWVETDLDPSDLTIQCTVNGEQRQLGRTTEMVRSVEDLIVHISEAMTLLPGDVILTGTPAGVGPLNVGDEVAVTIEGIGTLTNRVIKRG
>NZ_CP029192.1|WP_150216001.1|2693036_2693237_-|hypothetical-protein
MKTVKSTMFRNIANPRRTTLAHLTDADEVQAAAERPEHAVELPTQTANPKRTILMDAPEQATPVAG

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_CP029192_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_2

3947176-3947279

Orphan

Consensus_repeat	Method
CGCCCTTTCCGGGCAGGAGCACCGAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_2

>merge|NZ_CP029192|2|3947176-3947279|CRISPRCasFinder
CGCCCTTTCCGGGCAGGAGCACCGACCCCGCCGCTCCGCGGCGGATCACTCCCACCCACCCGCCCGTTCACCCCGCACCGCCCTTTCCGGGTAGGAGCACCGAC

>NZ_CP029192|2|1|3947176-3947279|CRISPRCasFinder
CGCCCTTTCCGGGCAGGAGCACCGAC	CCCGCCGCTCCGCGGCGGATCACTCCCACCCACCCGCCCGTTCACCCCGCAC
CGCCCTTTCCGGGTAGGAGCACCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150216994.1\|3955567_3957028_-\|menaquinone-biosynthesis-decarboxylase	unknown	unknown	gnl\|CDD\|163413
NZ_CP029192.1\|WP_150216993.1\|3954665_3955571_-\|4-hydroxybenzoate-octaprenyltransferase	unknown	unknown	gnl\|CDD\|183814
NZ_CP029192.1\|WP_150216988.1\|3949302_3950721_-\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|224220
NZ_CP029192.1\|WP_150216989.1\|3951073_3951373_-\|DUF4229-domain-containing-protein	unknown	unknown	gnl\|CDD\|379415
NZ_CP029192.1\|WP_150216984.1\|3941904_3942765_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|375319
NZ_CP029192.1\|WP_150216986.1\|3945848_3947162_+\|3-oxoacyl-ACP-reductase	unknown	unknown	gnl\|CDD\|236207
NZ_CP029192.1\|WP_150216983.1\|3940293_3941712_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP029192.1\|WP_150216992.1\|3953965_3954640_-\|UbiX-family-flavin-prenyltransferase	unknown	unknown	gnl\|CDD\|223241
NZ_CP029192.1\|WP_150216990.1\|3951491_3952016_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP029192.1\|WP_150216979.1\|3936172_3936958_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|237187
NZ_CP029192.1\|WP_150221227.1\|3934992_3936069_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	unknown	unknown	gnl\|CDD\|176198
NZ_CP029192.1\|WP_150221228.1\|3942821_3944333_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|312032
NZ_CP029192.1\|WP_150216981.1\|3938149_3939160_+\|3-oxoacyl-ACP-synthase	unknown	unknown	gnl\|CDD\|238423
NZ_CP029192.1\|WP_150216982.1\|3939227_3940268_+\|transaldolase	unknown	unknown	gnl\|CDD\|235117
NZ_CP029192.1\|WP_030791839.1\|3953257_3953713_-\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|214628
NZ_CP029192.1\|WP_150216985.1\|3944495_3945776_-\|acetyl-CoA-C-acetyltransferase	unknown	unknown	gnl\|CDD\|236440
NZ_CP029192.1\|WP_150221229.1\|3948394_3949030_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP029192.1\|WP_150216980.1\|3936991_3938113_+\|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	unknown	unknown	gnl\|CDD\|319968
NZ_CP029192.1\|WP_150216991.1\|3952029_3953193_-\|aminofutalosine-synthase-MqnE	unknown	unknown	gnl\|CDD\|213851
NZ_CP029192.1\|WP_150216987.1\|3947547_3948432_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239537

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150216994.1\|3955567_3957028_-\|menaquinone-biosynthesis-decarboxylase	gnl\|CDD\|163413	TIGR03701, mena_SCO4490, menaquinone biosynthesis decarboxylase, SCO4490 family. Members of this protein family are putative decarboxylases involved in a late stage of the alternative pathway for menaquinone, via futalosine, as in Streptomyces coelicolor and Helicobacter pylori. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP029192.1\|WP_150216993.1\|3954665_3955571_-\|4-hydroxybenzoate-octaprenyltransferase	gnl\|CDD\|183814	PRK12888, ubiA, 4-hydroxybenzoate octaprenyltransferase.	6.25138e-175
NZ_CP029192.1\|WP_150216988.1\|3949302_3950721_-\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|224220	COG1301, GltP, Na+/H+-dicarboxylate symporters [Energy production and conversion].	6.78798e-113
NZ_CP029192.1\|WP_150216989.1\|3951073_3951373_-\|DUF4229-domain-containing-protein	gnl\|CDD\|379415	pfam14012, DUF4229, Protein of unknown function (DUF4229). This family of integral membrane proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 95 and 122 amino acids in length.	4.00907e-16
NZ_CP029192.1\|WP_150216984.1\|3941904_3942765_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|375319	pfam17765, MLTR_LBD, MmyB-like transcription regulator ligand binding domain. This domain is found in a family of actinobacterial transcription factors. The structure shows it has a PAS domain like fold and it is bound to Myristic acid.	5.0805e-50
NZ_CP029192.1\|WP_150216986.1\|3945848_3947162_+\|3-oxoacyl-ACP-reductase	gnl\|CDD\|236207	PRK08261, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	0
NZ_CP029192.1\|WP_150216983.1\|3940293_3941712_-\|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].	5.74547e-55
NZ_CP029192.1\|WP_150216992.1\|3953965_3954640_-\|UbiX-family-flavin-prenyltransferase	gnl\|CDD\|223241	COG0163, UbiX family flavin prenyltransferase [Coenzyme transport and metabolism].	5.82065e-67
NZ_CP029192.1\|WP_150216990.1\|3951491_3952016_-\|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.	1.32305e-09
NZ_CP029192.1\|WP_150216979.1\|3936172_3936958_+\|SDR-family-oxidoreductase	gnl\|CDD\|237187	PRK12743, PRK12743, SDR family oxidoreductase.	5.70971e-94
NZ_CP029192.1\|WP_150221227.1\|3934992_3936069_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	gnl\|CDD\|176198	cd08236, sugar_DH, NAD(P)-dependent sugar dehydrogenases. This group contains proteins identified as sorbitol dehydrogenases and other sugar dehydrogenases of the medium-chain dehydrogenase/reductase family (MDR), which includes zinc-dependent alcohol dehydrogenase and related proteins. Sorbitol and aldose reductase are NAD(+) binding proteins of the polyol pathway, which interconverts glucose and fructose. Sorbitol dehydrogenase is tetrameric and has a single catalytic zinc per subunit. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Related proteins include threonine dehydrogenase, formaldehyde dehydrogenase, and butanediol dehydrogenase. 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. Horse liver alcohol dehydrogenase is a dimeric enzyme and each subunit has two domains. The NAD binding domain is in a Rossmann fold and the catalytic domain contains a zinc ion to which substrates bind. There is a cleft between the domains that closes upon formation of the ternary complex.	3.59984e-65
NZ_CP029192.1\|WP_150221228.1\|3942821_3944333_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|312032	pfam08386, Abhydrolase_4, TAP-like protein. This is a family of putative bacterial peptidases and hydrolases that bear similarity to a tripeptidyl aminopeptidase isolated from Streptomyces lividans. A member of this family is thought to be involved in the C-terminal processing of propionicin F, a bacteriocidin characterized from Propionibacterium freudenreichii.	1.18846e-24
NZ_CP029192.1\|WP_150216981.1\|3938149_3939160_+\|3-oxoacyl-ACP-synthase	gnl\|CDD\|238423	cd00827, init_cond_enzymes, "initiating" condensing enzymes are a subclass of decarboxylating condensing enzymes, including beta-ketoacyl [ACP] synthase, type III and polyketide synthases, type III, which include chalcone synthase and related enzymes. They are characterized by the utlization of CoA substrate primers, as well as the nature of their active site residues.	4.86903e-36
NZ_CP029192.1\|WP_150216982.1\|3939227_3940268_+\|transaldolase	gnl\|CDD\|235117	PRK03343, PRK03343, transaldolase; Validated.	2.05237e-43
NZ_CP029192.1\|WP_030791839.1\|3953257_3953713_-\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|214628	smart00344, HTH_ASNC, helix_turn_helix ASNC type. AsnC: an autogenously regulated activator of asparagine synthetase A transcription in Escherichia coli).	1.71692e-34
NZ_CP029192.1\|WP_150216985.1\|3944495_3945776_-\|acetyl-CoA-C-acetyltransferase	gnl\|CDD\|236440	PRK09268, PRK09268, acetyl-CoA C-acetyltransferase.	0
NZ_CP029192.1\|WP_150221229.1\|3948394_3949030_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	2.3205e-13
NZ_CP029192.1\|WP_150216980.1\|3936991_3938113_+\|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	gnl\|CDD\|319968	cd16361, VOC_ShValD_like, vicinal oxygen chelate (VOC) family protein similar to Streptomyces hygroscopicus ValD protein. This subfamily of vicinal oxygen chelate (VOC) family protein includes Streptomyces hygroscopicus ValD protein and similar proteins. ValD protein functions in validamycin biosynthetic pathway. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	2.11292e-40
NZ_CP029192.1\|WP_150216991.1\|3952029_3953193_-\|aminofutalosine-synthase-MqnE	gnl\|CDD\|213851	TIGR03700, mena_SCO4494, putative menaquinone biosynthesis radical SAM enzyme, SCO4494 family. Members of this protein family appear to be involved in menaquinone biosynthesis by an alternate pathway via futalosine, based on close phylogenetic correlation with known markers of the futalosine pathway, gene clustering in many organisms, and paralogy with the SCO4550 protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP029192.1\|WP_150216987.1\|3947547_3948432_+\|hypothetical-protein	gnl\|CDD\|239537	cd03453, SAV4209_like, SAV4209_like. Similar in sequence to the Streptomyces avermitilis SAV4209 protein, with a hot dog fold that is similar to those of (R)-specific enoyl-CoA hydratase, the peroxisomal Hydratase-Dehydrogenase-Epimerase (HDE) protein, and the fatty acid synthase beta subunit.	5.46424e-11

>NZ_CP029192.1|WP_150216986.1|3945848_3947162_+|3-oxoacyl-ACP-reductase
MADRYLTFTATGPGRFLTRRLGLPRPTRLRRWTPENPYLTGDLLLLSPTTASPCAPDLRTLLSTSLNVTSTSARPTAVVVDATAVTDTRSLTEVYAALHPVVRDVADNGRILIVGSPPDPADHHQAAAQQALEGFLRSLAKEVGRGRTANLVRVSGPMATAESTLRFLLSPKSAYVTGQVVETGPAETVAAPADRDRPLAGRTALVTGAARGIGAAVAEVLTRDGARVTLLDVPSAQPDLTRLADRLDGGTALPLDITAHDAGERIAAALPDGLDILVHNAGITRDRKLANMDRDRWTSVLDVNLTSVLTVTDTLLKTGTIRRGGCVVATASIAGIAGNAGQTNYAASKAGVIGLVRSLGPRALVEHGVAVNAVAPGFIETKMTAAVPLLIREAGRRMNSLAQGGLPVDVAETASWLAQGGLNAQTIRVCAQSLLGA
>NZ_CP029192.1|WP_150216985.1|3944495_3945776_-|acetyl-CoA-C-acetyltransferase
MSLPSVRRVAVLGGSRVPFARSDGPYATASNQDMLTAVVDGLVERHGLRGRGVVGELVAGAVLKHSRDFNLAREVVLGSALDSRTPAYDLQQACGTGLQAVVAVANKVMLGQVESGIAGGSDTASDAPLGVNDELRRVLLAARRATSVGGRLRALGGVRPRHLVPDIPRNAEPRTGLSMGEHAAVTARAWGITRAAQDELAAASHQRLAAAYERGLLDDLVVPYEGLTRDQNLRPGSTVEQLGRLKPVFGVAAGGATMTAGNSTPLTDGAAVVLLGSDEWAAGRGLEPLAHLVACETAAVDFVHGDVAGGDDGLLMAPAYAVPRMLERVGLGLGDFDFVEVHEAFASQVLATLAAWEKQGLGTVDRERLNVAGSSLATGHPFAATGARIVATLAKLLAERGRPGRGLISICAAGGQGVTAILERSQ
>NZ_CP029192.1|WP_150221228.1|3942821_3944333_-|alpha/beta-fold-hydrolase
MAAAGDESGRPDLARYYTQKIKWGTCKGDTEAMAEATGGAKDIRCGHVSVPLDYADPASGDVDVAMIRMKSSASGKPRGSLLLNFGGPGGPGVSALAGAQKDFGFLSKDYDVVSFDPRGVGLSEPVSCGDADKSTDPSSGGTGDAAAVLAEMRNVAAECAKKSGPVLPHMGTVNVSRDLDVMRQALGDKKLNYLGFSYGTRLGAVYAAQFPKNVGRMVLDGVDTLTEPVAEQSLVTAEGRQTALDNFLTWCTGNAGCVFGTDSRSARKGMVRLIKDMDQMPLRSLDGAEFTGQDVVGVLGQALYSRQAWPALSQALGALLADGDPRALIRMSGGLVPTGIPATGPATGPAAGEEVPADNMAAALMGVNCADDPDRPDAAHIEKEVGKLQKQFDDASPVFGKSMLMPVLLCFGRPAGTKYIREDVRDVKTPKLLLVGTRGDPATPYRWTEETARRLGSQAVVLDNKGDGHTGYLGSTCVQDKVNGFLLYGETPKSGESCAADEG
>NZ_CP029192.1|WP_150216984.1|3941904_3942765_+|helix-turn-helix-domain-containing-protein
MTTTTTGIAPSPGTELGRYLRARRARVAPAEAGLPAGTGFRRTPGLRREELATLAGVSVDYYTRLERGRETNPSPAVIDALARALRLSGDSHERLRDLAELSSGRLTEPHPTADHTVRDSTLRTLDALAPLPAYVVSRHSHMLAANAPGKALLPGLWEWPAERRNVLRYLFLHPVGRVLYQPWEETVAKSVSHLRAIGGTDTDSPQLTNLVGELLLKSPDFARIWERYDVCERGGGIKTFEHPKVGPMTLTYEVMTLARTGGQRMVVYQAPRNTPDETAMLRLTAG
>NZ_CP029192.1|WP_150216983.1|3940293_3941712_-|MFS-transporter
MAVPTLVPSARVPRSPDAPRASSSGSLALVASLLGFAVITIDVTAVNIALPDIRATLHGGMAGLQWVVDAYTLMFAALMLSAGALADRAGARRAYALGVGVFTAASLACALAPGIGALIAARVAQGAGAAIVMPASLSLIRQAYDDPRRRARAIALWTVGGSVSVAVGPVLGGVLTEAAGWRSVFLLNLPVGALILVLLARVARSPRRPAAVDLGGQVTAVLALAGLAFAVIEGGHMGWTSAPVVAGFGVAVVCAVAFHRVEKRHPAPMVPLSLLRQRQVGVALAVGFAVNAGFYGVTFLLGLYYQQLRGMSGVAAGLMFVPLAAIITGTNLVSPRAAERFGRRTVIVLGQAVLALAMFALVPLDADTPLWLVLVLLVPTGLGGAFAVPALTAQLLDSVPGERAGTASGMLNSLRQTGGAMSVALFGALIAGGGDGGVGGGFSLSGMHGGLVVAGLVLCATTALAAWMLPRD
>NZ_CP029192.1|WP_150216982.1|3939227_3940268_+|transaldolase
MNHAWKRLRAEGVDVWIDVSATAGGAAREVRRALAQGEVAGARMDVPREDPAAGHAPAAEIRRVCDQLLPRHRASGGTGGLVSVPLPAGAAPDPAAWAARARALRDEIDRPNLVVRLPAEAADTATLRALFALDVAVEVSGVCSPRRYGEAATALLSALDGPARTASFVSFDVTGVERHVDARLDLIGSDEAKALRGRAGLACARLAHRAHEMTFSSARWGALAAAGTPEPKLLWVTGGASPYRSAYYVQELVTRGTATAMRPAAADALAEAGTVSGDRVWRHYADAERTLAYLNWFGISVETLAAGPQSPPAALADPPAPRETASHPPAHPHRGAHQSHRRLTPA
>NZ_CP029192.1|WP_150216981.1|3938149_3939160_+|3-oxoacyl-ACP-synthase
MRWTDIYVESAAAEFGKLQTGQEAVDLGLLPAEEIVRSAQRSVSVSDGRSGPELAVAAGRTALARAGRDARDVGLLIHADCWYQGLEFWNTAAYVQDQVLGHGDCVAYELRQMSNGGMSALENAAARLTAIPATRAALVTTGDRFADPAFPRWSTDRGLAFGDAGTAVVLSRTPGALRLVATSSYSQPMLEGLHRGAEPFLPSGSETGPLDLVARKKGFLRGRSQEEITTRNETGMMSAVKTCLAEADTDIAGMKAVVVPFFGARLSRLQCLAPLGIQPEVTLQEFGLTVGHLGAGDQAAGLAKLLEDDTLESGDQVLLVGVGAGFSWTCAVLERS
>NZ_CP029192.1|WP_150216980.1|3936991_3938113_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein
MSPTAPSDTRAAATGRTADGLSIPTARNVDHYAYTVADLDTAVDFCTTVLGADVLYRLGPVEEPDSDWMARQLGVHPRASTNIAMLRLGPDSNLELFQYTAPEQRTQAPEFTDVGGHHIGIHVSDLDVALAKAERSPHVRVLGEPHTDTGGPTAGNRWIHLLTSWGMRLELRELATELPYEKETEARVYRPAGDWPRGLPGSLGIGHVGYSVADLDEAVAFFTGPMGGELAYRTSESVDAGTARRQYAVTSPFRKDTAAIRLGPVTTVELSSYEIEGRRTERPRNSDVGGHHLAFFVDDVERAAAWLAATDGAEVLGEPQLIEDGGPIHGDRWVYFRGVGGFQLEVLNMPPGMPYEQHTAARRFGPSPRWTNR
>NZ_CP029192.1|WP_150216979.1|3936172_3936958_+|SDR-family-oxidoreductase
MNRPIAVVTGASSGIGAAVAEALAAAGFDLVVGYGRQADAAKEIADGLAVRHGVRAETLGLDLTDPAAAGEALRDRVDAFGGIDVLVNNAGLNRRASVVEETLQDWQRILDVNLTSPFRLSQVAAARMIAQGRGGRIINITSIHEHIPIGEGSTYCAAKGGLGALTKAMALDLAGHGITVNAVAPGETATPMNNVPAGLDAADIARPAIPAGRPGRPDEVAALVAYLASPAAAYTTGTSTLVDGGMALSAAVANAAHAGTV
>NZ_CP029192.1|WP_150221227.1|3934992_3936069_+|alcohol-dehydrogenase-catalytic-domain-containing-protein
MLPPTDDLLCGRWPNGSMKAAAVMDVNKVGQVEVEIPGPELGYVLVAPTTVGICGTDLELLHGTASYVRDGRATMPHVFGHEWVGRVVAIAGNCQYSRQLQIGDRVVGQTMLSCGGCRACQRGHRNECSQLKEVGLYGQQGAAAEFIRLPAQSLTKVPPGVDDFSAALAEPAVTVLAALDKVGVFPGERVLVFGTGTMGLLAVQMARRVAGTVDVVGIDDAGIGAALRMGAEHAFLPGEARDGDYDVVIEASGAVPALLEALRVADVGGRIAAVGVPNDPLPAVDASELVLRGVTMTGVRHGLDYYERALRLFSEGVLSAKGMIADVFELADVDKAFELLERGRRAAPKVALSLTPRP
>NZ_CP029192.1|WP_150216987.1|3947547_3948432_+|hypothetical-protein
MPPALAVLRAALRRTHSRPDPSAPPPPTRLTTTRTTDPDHLAAYRRLCGFPAGHATLPLPYPHVLAFPLSMRLMTGRDFPLPLLGLVHTSIEIDQYKPIRSTEELHLSVRTTALTPHRRGTEATLLTEAASADGELLWQSRSTYLARHKTRPTSTASAPRTEPESAPEPESAPAPAPGENWQLPAGLGRRYASVSGDRNPIHLHALTARPFGFPRAIAHGMWTAARCLAEQERGETRTPTHTHAPTHTRIEFKAPVPLPTTVTYSTPTPHTFELRSPQGKLHLTGATGPTDAPP
>NZ_CP029192.1|WP_150221229.1|3948394_3949030_-|TetR-family-transcriptional-regulator
MPRAVREQQMLDAAVRTFGQRGYRAASMDEIAELAGVSKPLVYLYLNSKEELFSACIRREAAALVAAVRGADGGAAAPGPVPADRQLWDGLRAFFTHTAERPDGWAVLHSQARTQGEPFAAEVAAMREEIVSFVTTLIAEAARAAHGDPSLPEREVAGLAQALVGAAESLAGWANVEGAVSAKEAAATLMNFAWAGLGGLMEGRRWVPSPL
>NZ_CP029192.1|WP_150216988.1|3949302_3950721_-|cation:dicarboxylase-symporter-family-transporter
MSANSATPADKAGTTEKPQSGFRIPKFLKIPFWAQILGGLVLGVLLGWLARSQDISWLVTTLSKVGDTFIGLLKLAVAPLVFFAILVSITNLRKVNNAARLATRTLLWFMITSLIAVAIGLAIGLLTNPGSGTGLTPKDGKAPDHAGSWIDFLTGIIPTDVITPFTQLNVLQIVFMAAVAGIAVLKIGDKAQPILELSESVLALLQKALWWVIKLSPIGTIGLIGFAIADYGWNLISKYATFTADIYIGCALVLFGVYPLLLAFVAKVNPLQFFKGAWPAIQLAFVSRSSVGTMPITQKVTERLGVPKEYTSFAVPFGATTKMDGCAAIYPSIAAIFVAQIFDVNLGIKEYLLIAFVSVVGSAATAGLTGATVMLTLTLSTLGLPMEGVGLLLAIDPVLDMMRTATNVAGQALVPVVVAAREKILDREAYERASASSLEEFDSSESTDSVGSSDSVDTPEDARPSRKVPAAV
>NZ_CP029192.1|WP_150216989.1|3951073_3951373_-|DUF4229-domain-containing-protein
MLRYTLMRLGIFVGCFLVVWGLVYSEILPRGLGESNLLWVLLLALVISAPISFVVLRKERDRASETVVARVDRAKANLEANRTQEDEADDVARAQAQGS
>NZ_CP029192.1|WP_150216990.1|3951491_3952016_-|GNAT-family-N-acetyltransferase
MSLVFRLDPPVDPALRDGVLALWADVTNAGGAVGFVPPTTPEEIRPEFVRHLAAMSEGRTRLLVGYDEEGAVAATAFLTHNTHRLMRHWIWLYTVMVHPRHQGKGYGRDLMAAVDDAARSLEGTDAIRLTCRGGTGLEHFYASCGYKEVGRVPGAIRVAPGDDRDDIMLLRELR
>NZ_CP029192.1|WP_150216991.1|3952029_3953193_-|aminofutalosine-synthase-MqnE
MDAGLKRELEQKVRDGERLSREDGIALYESDDLAWLGGLAHEVRTRKNGDVVHFNVNRHLNMTNVCTASCAYCSFQRKPGEKDAYTMRIEEAVRLAKAMEGENLTELHIVNGLHPNLPWRYYPRSLSELKKALPDVSLKAFTATEIHHFETISGMPASEILDELIEAGLESLTGGGAEIFDWEVRQHIVDHRTHWEDWSRIHRLAHEKGLKTPSTMLYGHIEERRHRVDHVLRLRELQDETGGFQVFIPLRYQHDFVDMQDGKVRNRLQARTKMASGAEALKTFAVSRLLFDNVPHVKVFWVMHGLHTTQLALQHGADDMDGSVVEYKITHDADNFGTPNKLTREDLLDLIREAGFRPVERNTRYEAIREYEGPDPLLRETPQAMRV
>NZ_CP029192.1|WP_030791839.1|3953257_3953713_-|Lrp/AsnC-family-transcriptional-regulator
MDAVDRQLIQALRENGRASYAELGRLVGLSGPSVTDRINRLEAAGVITGYRATVDSASLGLGVIALIGISLSDAADHEDVARRLKDLHEIEDCWFIAGDDSYMLKVRASDVDGLEKTIRRLSGTRGVSRTRTTIVLSTKWENRVGELPEEE
>NZ_CP029192.1|WP_150216992.1|3953965_3954640_-|UbiX-family-flavin-prenyltransferase
MNPGDTQRRPWIVGVSGASGTPYAAAVLRALLAAGESVDLVVSRASRLTLLDETGIAFRDAHWRDDLRQWLARGADGKPGVFDPDVSDVRYWSAGDLAAGPSSGSYATKGMLIVPASTACVAGVALGLSKDLLQRSASVTLKEGRRLVVCVRETPLNGQTLKHLVSLDEAGAIVLPASPAFYAGATHIQDLVDFVAGRVLDAARVPHSLYRRWEGELGSGSQGG
>NZ_CP029192.1|WP_150216993.1|3954665_3955571_-|4-hydroxybenzoate-octaprenyltransferase
MSSASAAIPQQPGRTKAFLRLVMIEHSVFALPFAYIAALTAMFRLDGNIHWGRLLLVTICMVGLRTFAMAANRIIDREIDARNPRTAHRELVTGAVSVKSAWTGALIALVVFLGSAALLNPLCLALAPVAVVPMVVYPYGKRFTNFPQAILGLAQAIGPIGAWLAVTGEWSWQAVILGLAVGIWIGGFDLIYACQDVETDREVGVKSVPARFGIPAAIRGARGCHLVTTALFVWYAAATDAGVFFWLGIAIVAGAFVYEHSIVKPHDLSRLNRAFFQVNGFIGIALFACALLDLLVRGLTV
>NZ_CP029192.1|WP_150216994.1|3955567_3957028_-|menaquinone-biosynthesis-decarboxylase
MAYDDLRSLLRALDREGDLKRIKAEVDPYLEVGEITDRVQKAGGPALLFENVKGSAMPLAMNVYGTDRRLLKALGLKSYNEISEKIGGLLKPELPHGFVGVREAFGKLGAMTHVPPKKVKGENAPVQETVLTGDDVDLEQLPALFTWPEDGGSFFNLGLTHTKDPDTGVRNLGLYRLQRHDKRTIGMHWQIHKDSRNHYQVAARRGEKLPVAIAFGCPPAVTYASTAPLPGDMDEYMLAGFIQGKRVEMVDCKTVPLQVPAHAEVVIEGWLEPGEMLPEGPFGDHTGFYTPQEPFPALKIDCVTMRKRPLLQSIVVGRPPTEDGPLGRATERFFLPLLKVIVPDIVDYHLPESGGFHNCAIVSIDKKYPKHAQKVMHAIWGAHMMSLTKLIIVVDKDCDVHNLHEVSWRALGNTDYARDLTVVEGPVDHLDHASYQQFWGGKAGIDATKKLPEEGYVRDGGWPNMVESDPSIAAKVDRRWKEYGLS

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_CP029192_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_3

4182718-4182837

Orphan

Consensus_repeat	Method
TCCGAGGATCCCGATCCCTCCGGG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP029192_3

>merge|NZ_CP029192|3|4182718-4182837|CRISPRCasFinder
TCAGAGAATCCCGCGCCGTCCGACGCAGCGAACTCCACGCCCTCCGAGGATCCCGATCCCTCCGGGAACCTCGCCCCGTCCGGGGACCACGATCCATCCGAGGACCCCGATCCCTCCGGG

>NZ_CP029192|3|2|4182718-4182837|CRISPRCasFinder
TCAGAGAATCCCGCGCCGTCCGAC	GCAGCGAACTCCACGCCC
TCCGAGGATCCCGATCCCTCCGGG	AACCTCGCCCCGTCCGGGGACCACGATCCA
TCCGAGGACCCCGATCCCTCCGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150217170.1\|4192416_4192881_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217169.1\|4191388_4191832_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_003975360.1\|4180422_4180584_-\|DUF4177-domain-containing-protein	unknown	unknown	gnl\|CDD\|379366
NZ_CP029192.1\|WP_150217164.1\|4180666_4181647_+\|P-loop-NTPase	unknown	unknown	gnl\|CDD\|223082
NZ_CP029192.1\|WP_150217168.1\|4190026_4191151_-\|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|99812
NZ_CP029192.1\|WP_150217166.1\|4183870_4186159_+\|penicillin-binding-protein	unknown	unknown	gnl\|CDD\|223815
NZ_CP029192.1\|WP_150185357.1\|4186276_4186741_-\|GatB/YqeY-domain-containing-protein	unknown	unknown	gnl\|CDD\|370480
NZ_CP029192.1\|WP_076685181.1\|4183142_4183538_-\|WhiB-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376791
NZ_CP029192.1\|WP_150217171.1\|4193175_4193748_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221243.1\|4188896_4189982_-\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|239583
NZ_CP029192.1\|WP_150217167.1\|4186872_4187799_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|224326
NZ_CP029192.1\|WP_150188347.1\|4183428_4183641_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217163.1\|4179955_4180426_-\|RidA-family-protein	unknown	unknown	gnl\|CDD\|100006
NZ_CP029192.1\|WP_079075134.1\|4173582_4173771_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217160.1\|4175870_4176872_-\|endonuclease-III	unknown	unknown	gnl\|CDD\|223255
NZ_CP029192.1\|WP_016642758.1\|4177231_4177906_+\|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223736
NZ_CP029192.1\|WP_150221242.1\|4175044_4175758_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239518
NZ_CP029192.1\|WP_150217159.1\|4173790_4174996_-\|MarP-family-serine-protease	unknown	unknown	gnl\|CDD\|367140
NZ_CP029192.1\|WP_150217161.1\|4178020_4178851_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293836
NZ_CP029192.1\|WP_150217162.1\|4178948_4179827_-\|NUDIX-hydrolase	unknown	unknown	gnl\|CDD\|239518

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_003975360.1\|4180422_4180584_-\|DUF4177-domain-containing-protein	gnl\|CDD\|379366	pfam13783, DUF4177, Domain of unknown function (DUF4177).	0.000161009
NZ_CP029192.1\|WP_150217164.1\|4180666_4181647_+\|P-loop-NTPase	gnl\|CDD\|223082	COG0003, ArsA, Predicted ATPase involved in chromosome partitioning [Cell division and chromosome partitioning].	3.2048e-33
NZ_CP029192.1\|WP_150217168.1\|4190026_4191151_-\|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	gnl\|CDD\|99812	cd06216, FNR_iron_sulfur_binding_2, Iron-sulfur binding ferredoxin reductase (FNR) proteins combine the FAD and NAD(P) binding regions of FNR with an iron-sulfur binding cluster domain. Ferredoxin-NADP+ (oxido)reductase is an FAD-containing enzyme that catalyzes the reversible electron transfer between NADP(H) and electron carrier proteins such as ferredoxin and flavodoxin. Isoforms of these flavoproteins (i.e. having a non-covalently bound FAD as a prosthetic group) are present in chloroplasts, mitochondria, and bacteria in which they participate in a wide variety of redox metabolic pathways. The C-terminal domain contains most of the NADP(H) binding residues and the N-terminal domain interacts non-covalently with the isoalloxazine rings of the flavin molecule which lies largely in a large gap betweed the two domains. Ferredoxin-NADP+ reductase first accepts one electron from reduced ferredoxin to form a flavin semiquinone intermediate. The enzyme then accepts a second electron to form FADH2 which then transfers two electrons and a proton to NADP+ to form NADPH.	2.42864e-105
NZ_CP029192.1\|WP_150217166.1\|4183870_4186159_+\|penicillin-binding-protein	gnl\|CDD\|223815	COG0744, MrcB, Membrane carboxypeptidase (penicillin-binding protein) [Cell envelope biogenesis, outer membrane].	3.0384e-159
NZ_CP029192.1\|WP_150185357.1\|4186276_4186741_-\|GatB/YqeY-domain-containing-protein	gnl\|CDD\|370480	pfam09424, YqeY, Yqey-like protein. The function of this domain found in the YqeY protein is uncertain.	3.07115e-45
NZ_CP029192.1\|WP_076685181.1\|4183142_4183538_-\|WhiB-family-transcriptional-regulator	gnl\|CDD\|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	2.94899e-27
NZ_CP029192.1\|WP_150221243.1\|4188896_4189982_-\|acyl-CoA-desaturase	gnl\|CDD\|239583	cd03506, Delta6-FADS-like, The Delta6 Fatty Acid Desaturase (Delta6-FADS)-like CD includes the integral-membrane enzymes: delta-4, delta-5, delta-6, delta-8, delta-8-sphingolipid, and delta-11 desaturases found in vertebrates, higher plants, fungi, and bacteria. These desaturases are required for the synthesis of highly unsaturated fatty acids (HUFAs), which are mainly esterified into phospholipids and contribute to maintaining membrane fluidity. While HUFAs may be required for cold tolerance in bacteria, plants and fish, the primary role of HUFAs in mammals is cell signaling. These enzymes are described as front-end desaturases because they introduce a double bond between the pre-exiting double bond and the carboxyl (front) end of the fatty acid. Various substrates are involved, with both acyl-coenzyme A (CoA) and acyl-lipid desaturases present in this CD. Acyl-lipid desaturases are localized in the membranes of cyanobacterial thylakoid, plant endoplasmic reticulum (ER), and plastid; and acyl-CoA desaturases are present in ER membrane. ER-bound plant acyl-lipid desaturases and acyl-CoA desaturases require cytochrome b5 as an electron donor. Most of the eukaryotic desaturase domains have an adjacent N-terminal cytochrome b5-like domain. This domain family has extensive hydrophobic regions that would be capable of spanning the membrane bilayer at least twice. Comparison of sequences also reveals the existence of three regions of conserved histidine cluster motifs that contain the residues: HXXXH, HXX(X)HH, and Q/HXXHH. These histidine residues are reported to be catalytically essential and proposed to be the ligands for the iron atoms contained within the homolog, stearoyl CoA desaturase.	3.03498e-46
NZ_CP029192.1\|WP_150217167.1\|4186872_4187799_+\|metallophosphoesterase	gnl\|CDD\|224326	COG1408, COG1408, Predicted phosphohydrolases [General function prediction only].	1.37513e-45
NZ_CP029192.1\|WP_150217163.1\|4179955_4180426_-\|RidA-family-protein	gnl\|CDD\|100006	cd02199, YjgF_YER057c_UK114_like_1, This group of proteins belong to a large family of YjgF/YER057c/UK114-like proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	3.55053e-68
NZ_CP029192.1\|WP_150217160.1\|4175870_4176872_-\|endonuclease-III	gnl\|CDD\|223255	COG0177, Nth, Predicted EndoIII-related endonuclease [DNA replication, recombination, and repair].	1.42918e-103
NZ_CP029192.1\|WP_016642758.1\|4177231_4177906_+\|Crp/Fnr-family-transcriptional-regulator	gnl\|CDD\|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	3.31367e-52
NZ_CP029192.1\|WP_150221242.1\|4175044_4175758_-\|NUDIX-domain-containing-protein	gnl\|CDD\|239518	cd03426, CoAse, Coenzyme A pyrophosphatase (CoAse), a member of the Nudix hydrolase superfamily, functions to catalyze the elimination of oxidized inactive CoA, which can inhibit CoA-utilizing enzymes. The need of CoAses mainly arises under conditions of oxidative stress. CoAse has a conserved Nudix fold and requires a single divalent cation for catalysis. In addition to a signature Nudix motif G[X5]E[X7]REUXEEXGU, where U is Ile, Leu, or Val, CoAse contains an additional motif upstream called the NuCoA motif (LLTXT(SA)X3RX3GX3FPGG) which is postulated to be involved in CoA recognition. CoA plays a central role in lipid metabolism. It is involved in the initial steps of fatty acid sythesis in the cytosol, in the oxidation of fatty acids and the citric acid cycle in the mitochondria, and in the oxidation of long-chain fatty acids in peroxisomes. CoA has the important role of activating fatty acids for further modification into key biological signalling molecules.	8.93415e-51
NZ_CP029192.1\|WP_150217159.1\|4173790_4174996_-\|MarP-family-serine-protease	gnl\|CDD\|367140	pfam02674, Colicin_V, Colicin V production protein. Colicin V production protein is required in E. Coli for colicin V production from plasmid pColV-K30. This protein is coded for in the purF operon.	8.75586e-23
NZ_CP029192.1\|WP_150217161.1\|4178020_4178851_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293836	cd16278, metallo-hydrolase-like_MBL-fold, uncharacterized subgroup of the MBL-fold_metallo-hydrolase superfamily; MBL-fold metallo hydrolase domain. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) for which this fold was named perform only a small fraction of the activities 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.	4.97676e-76
NZ_CP029192.1\|WP_150217162.1\|4178948_4179827_-\|NUDIX-hydrolase	gnl\|CDD\|239518	cd03426, CoAse, Coenzyme A pyrophosphatase (CoAse), a member of the Nudix hydrolase superfamily, functions to catalyze the elimination of oxidized inactive CoA, which can inhibit CoA-utilizing enzymes. The need of CoAses mainly arises under conditions of oxidative stress. CoAse has a conserved Nudix fold and requires a single divalent cation for catalysis. In addition to a signature Nudix motif G[X5]E[X7]REUXEEXGU, where U is Ile, Leu, or Val, CoAse contains an additional motif upstream called the NuCoA motif (LLTXT(SA)X3RX3GX3FPGG) which is postulated to be involved in CoA recognition. CoA plays a central role in lipid metabolism. It is involved in the initial steps of fatty acid sythesis in the cytosol, in the oxidation of fatty acids and the citric acid cycle in the mitochondria, and in the oxidation of long-chain fatty acids in peroxisomes. CoA has the important role of activating fatty acids for further modification into key biological signalling molecules.	0.00234538

>NZ_CP029192.1|WP_150217164.1|4180666_4181647_+|P-loop-NTPase
MSRLQVVSGKGGTGKTTVAAALALALATEGKRTLLVEVEGRQGIAQLFETEALPYEERKIAVAPGGGEVYALAIDPELALLDYLQMFYKLGGAGRALKKLGAIDFATTIAPGLRDVLLTGKACEAVRRKDKRGRYTYDCVVMDAPPTGRITRFLNVNDEVAGLAKIGPIHNQAQAVMRVLKSPETAVHLVSLLEEMPVQETADGIAELRAAQLPVGRVIVNMVRPALLGDASLELGLDRTPRTAIAKTLSAAGLGGARRGGGAERLVDPLLEQAAEYAERYALERDQRAQLTEFGQPLHELPLLAGGMDLAGLYELATALRKQGIS
>NZ_CP029192.1|WP_003975360.1|4180422_4180584_-|DUF4177-domain-containing-protein
MTKWEYATVPLLVHATKQILDTWGEDGWELVQVVPGPNNPEQLVAYLKREKQA
>NZ_CP029192.1|WP_150217163.1|4179955_4180426_-|RidA-family-protein
MSGAVEARLAELGLTLPEVVPPLASYQPAVQSGVYVYTAGQLPMVEGKLAVTGKVGAEVTPEEAKDLARTCALNGLAAIKSVAGDLDRIARVVKVVGFVASATDFTGQPGVINGASELLGEVLGDKGVHARSAVGVAVLPLDAPVEVEFQVELTEA
>NZ_CP029192.1|WP_150217162.1|4178948_4179827_-|NUDIX-hydrolase
MANGQWYPPEWPDRIRALASGELTPATPRRAATVMLLRDGRDEAGNGAPEVHMLRRRASMAFAGGAYAYPGGGVDPRDDDQLVRWAGPTRASWADRLGVDDEAQAIVCAAVRETYEEAGVLLAGRTPDTVVGDTTGDDWESDREALVARELSFAQFLDHRNLYLRSDLLAAWARWITPEFEPRRYDTFFFVAALPEGQRTRNASTEADRTVWIRPSEAAARYDDGELLMMPPTIATLRSLSAHPTPRAALAAAPGQDMTPVLAQARLENDTLVLSWPGHDEFTKRVGAGGER
>NZ_CP029192.1|WP_150217161.1|4178020_4178851_-|MBL-fold-metallo-hydrolase
MTDAAALPGQPRGGVLSGPATARAVNVLAPNPSAMTLDGTNTWIVSEPDSPLAVVIDPGPQDDAHLSRVVETAEKMGKRVALTLLTHGHPDHAEGAARFAELTRTPVRALDPALRLGDEGLAPGDVITTGGLEMRVVATPGHTADSLCFHLPADQAVLTGDTILGRGTTVVAHPDGRLGDYLDSLRRLRSLTVDDGVHTVLPGHGPVLEDAQGAVEFYLAHRATRLAQVETAVENGHSEASDVVAHVYADVDRSLWPAAELSVRAQLDYLREHGLI
>NZ_CP029192.1|WP_016642758.1|4177231_4177906_+|Crp/Fnr-family-transcriptional-regulator
MDDVLRRAPLFAALDDEQAAELRASMSEVTLARGDALFHEGDPGDRLYVVTEGKVKLHRTSPDGRENMLAVLGPGELIGELSLFDPGPRTATASALTEVKLLGLGHGDLQPWLNARPEVAAALLRAVARRLRKTNDQMSDLVFSDVPGRVARALLDLSRRFGVQSEEGIHVVHDLTQEELAQLVGASRETVNKALADFAGRGWLRLEARAVILLDVERLAKRSR
>NZ_CP029192.1|WP_150217160.1|4175870_4176872_-|endonuclease-III
MSTKKTTKTTAKTAATKTTTATTPPAKSAAKKTAAPAKKAAAAKKATAPAKKVAAAKKAPAAKKATAAAANKAPAAKKPPESHAALVRRARRINRELADVYSYAHPELDFENPFELLVATVLSAQTTDLRVNQTTPRLFAKYPTPEDLAAAVPEEVEELIRPTGFFRAKTKSIMGLAKALRDDFGGEVPGRIDDLVKLPGVGRKTAFVVLGNAFGVPGITVDTHFGRLVRRWKWTEETDPVKVETAVAALFPKSEWTMLSHRVIFHGRRICHSRKPACGACPIAPLCPSYGEGETDPEKAKKLLKYEMGGFPGQRLKPPPDYPGKPAPPLAAG
>NZ_CP029192.1|WP_150221242.1|4175044_4175758_-|NUDIX-domain-containing-protein
MTRSTTQSTHGGRQPHEELLSTAGLPSWLDPVVHAAQTVQPLQLSRFLPPESGAGRQSAVLILFGEGEKGPEILLMERAGSLRSHAGQPSFPGGALDPEDGDPQGEGPLRAALREAEEETGLDPRGVQLFAELPRLFIPVSDFVVTPVLGWWRTPTPVGVVDPNETARVFTVPVADLTDPANRATAVHPSGHHGPAFLVESALVWGFTAGVIDRILHFAGWERPWDRSRQVPLDWRA
>NZ_CP029192.1|WP_150217159.1|4173790_4174996_-|MarP-family-serine-protease
MNMLDVLLLLAAVWFAVVGYRQGFVVGILSVIGFLGGGLVAVYLLPIVWDALNDDDAATVSTTAAVIAVVIVIVCASIGQAFTTHLGNKLRRYITWQPARALDATGGALVNVVAMLLVAWLIGSLLAGATLPTLGKEVRNSKVLLGVDRALPGQADTWFTDFSSVLARNGFPQVFSPFSDEPITEVKPPDPKLAKSAVATKAKRSIVKVRGEARSCGKVLEGTGFVFANRRVMTNAHVVGGVDDPTVQIGDQGQIYDAKVVLYDWERDIAVLDVPTLQAPALQFTSKDAASGVGAIVAGFPEDGPYDVRPARVRGRITAKGPDIYHRGTVRRDVYSLYATVRQGNSGGPLLTPEGKVYGVVFAKSLDDPDTGYALTADEVREDIEKGRTANQEVDSEGCAL
>NZ_CP029192.1|WP_079075134.1|4173582_4173771_+|hypothetical-protein
MGWTHDYSDVARNRRSATALNSRERGGPQDPGHHGPPQEMGIPRILRRRARWVSARLRHTRD
>NZ_CP029192.1|WP_076685181.1|4183142_4183538_-|WhiB-family-transcriptional-regulator
MPLPPWGSLDSGEDGAGMGWVTDWSAQAACRTTDPDELFVQGAAQNRAKAVCTGCPVRTECLADALDNRVEFGVWGGMTERERRALLRRRPTVTSWRRLLETARSEYERGAGLLPVDLEDEETYESYAAVG
>NZ_CP029192.1|WP_150188347.1|4183428_4183641_-|hypothetical-protein
MPLTHSPFGPFKIGPEGGVALCPPSVTSSTGGGAYAAAAVGEPRFGRGRRRYGLGNRLECAGGLPHYRSG
>NZ_CP029192.1|WP_150217166.1|4183870_4186159_+|penicillin-binding-protein
MGKKRSGGGLSPTQQAAKFLGVSVLAGAVLAGIALPAFGALGLAAKGSVEGFDEIPANLKQPPLSQRTSILDNKGGQIATVYSRDRTVVPLKDISPYMQKAIVAIEDARFYEHGAVDLKGILRALNQNAQSGGVSQGASTLTQQYVKNVFVEEAGDDPTKVAEATQQTIGRKVRELKYAIQVEEELGKKRILKNYLNITYFGQQAYGIEAASQRYFSKHAKDLEVQEAALLAGIVQSPSRYDPVNDAAEATKRRNVVLQRMAETHDITQAEADAAKKTDLGLNVSRPKNGCITSVKGAGFFCDYVREVFLNDPVFGKTKEDRAKVWNRGGLKVHTTLDPQAQDSVQASIKNHVNKTDDVATAAAIVEPGTGKIRGMGQSRPYGFKKDETTINLSVDDSMGGGAGYQPGSTFKPIVAAAALEGGKSAGQSYSSPYEMPYPERVSACGGKQWVNSGGDKLTNENESEVGPYGMREATAKSVNTYYVQLIGDIGICPVTQLAAKMGVERADGKKMDQAPSIALGTQEMSPLTMAGAYATFASRGTYCTPIAIESIATLGGKSLPVPKSTCSRAMSEKTADTINTLLKGVVEDGTGKQAGLGSRASAGKTGTTDYRYAAWFVGYTPNLSGAVWVGDPMHKRRMVDITIGGVPYGKVFGGEVPGPIWRDAMTGALAGKPAPNFRTVHIPGGDKDKDEDHGGDGGHDDGRPGDGGGLGGGGNGGGNGGGGGGGNPWPDISIPPGVLGGNGNGGNGNGFGGGIGGGWRR
>NZ_CP029192.1|WP_150185357.1|4186276_4186741_-|GatB/YqeY-domain-containing-protein
MTTLKSKLHEDLTAAIRGRDELRSSTLRLTLTAITKEEVAGKTARELSDDEVQKVIAREAKKRREAAEAFAEGGRAEQAAKEKAEGEILAEYLPKQLSDDELQDIVAQAVAEAKAAGAEGPRAMGQVMKIVNPKVAGLAEGGRVAATVKKLLAG
>NZ_CP029192.1|WP_150217167.1|4186872_4187799_+|metallophosphoesterase
MRARYAVPLGITATAAAGLAYSVGVEPRSFRLRRVTVPVLPPGMRSLRVLQVSDIHMVSGQRKKQRWLRSLAGLRPDIVINTGDNLSDPEGVPETLDALGPLMEFPGAYVFGSNDYYGPKPRNPGRYLIEKVQGRHGLNGNAPAVGVPRNPWEGLRDGFDAAGWVNLTNTRGALKIDGYEIAFTGLDDPHIKRDRYAEVAGGPDSGADFSMGIVHAPYLRSLDAFTADGYPLILAGHTHGGQLCIPFYGALVTNCDLDTDRVKGLSRHESEGRTSYLHVSAGCGANRYTPMRFACPPEATLLTLTARD
>NZ_CP029192.1|WP_150221243.1|4188896_4189982_-|acyl-CoA-desaturase
MPTAAAAGADGTPPPVASHADRAEQLGRELDRLRDEIVAARGPDDARYIRTVIAVQRGCEAGGRLALAVSLFPPAWAAGTALLAVAKTLENMELGHNILHGQWDWLGDPAVHSTTWEWDFAAPADAWKRTHNHLHHTYTNVVGRDRDLGYTILRMSPDQPWRPAHLLQPLYTALLAPVFEWGIALYDLEAEAVAQGRKSVRAFVRDASGVTRKAVRQAAKDYVLFPLLAGPSALPCLLGTLTANGARNIWAHTVIFCGHFPGDVQTFTEDQLDGETRGEWYLRQIQGSANIEGGPLLHLLTGNLSHQIEHHLFPDLPSNRYAQMAPRVREICDRYGLPYVTGPLWRQYASMWSRVLRHALP
>NZ_CP029192.1|WP_150217168.1|4190026_4191151_-|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein
MSVRPWLSPGALRPGTRATLTALSWLTSPLTPDDYLGLIDPLWSARHPAGRVSAVRREAPGAATLVIRPGRGWNGHRAGQYLPLGVEIDGVRHWRTYSITSPPGRSPGGGPGGEITVTVKARRDGRVSPHLVHRTAPGSVLRLGPAQGEFVLPRPLPGRLLFVTAGSGVTPVVGMLRTLARHGGAAPDTLLLHSAPSPDECLFHAELAALESRLPWLSVRLTYTRTEGRLTTERIGELCPDWHRRETWACGPSGLLDMAEGHWAAAGVREQLRVERFHLAPVRAPRADAVGGRVRFDRSAVEADAAAASPLLAVGESAGVPMPHGCRRGLCFGCLVPLLDGRVRDLRNGELRGEPGELIQTCVNGAAGPLVLDL
>NZ_CP029192.1|WP_150217169.1|4191388_4191832_-|hypothetical-protein
MTLTPPPLLPSPSLLRLRLAPHAGGPRAIDGAWWPRSYDLLAELPCLLAGLPRSWGHITSVVLNGAVWTPTPGRMFVAGQVVRLRRSLTATAAHTVVLLAPGHGRWDLLVVPPDATEEAAKPIMESVTGAGSVVASEPPVAIPRSRP
>NZ_CP029192.1|WP_150217170.1|4192416_4192881_+|hypothetical-protein
MNAPIVHRSSAGPGRRAMYPPARLVLRPPTFPQGPVCGAWWPRTDDLAAELAALTDVFDASHGLVTRIASHRGSWPHEPRTLPVTGHTVTASWYTSGLDPHTIRLFSCGARRWDLFVVPPRSGADAAARLMTAAADPASHLTGTALMATEVPPG
>NZ_CP029192.1|WP_150217171.1|4193175_4193748_+|hypothetical-protein
MTVLTARPPPTATAAKPSDCSPLRLSVKPPGPLSGLLDGAWWPRSRDLARELPALTDLLDPLWGRITRVSVNPTYWPGVPRKVPVKGHVVNVGWFRAEQDPHQLMLRSYRVGRWDLLIIPPEIGAEAAARLMATACDPRIVRTGSALVADELSRHPAAPAEADPPGRTQAESWEAEGGATAAPVGTTGGR

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_CP029192_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_4

4272400-4272511

Orphan

Consensus_repeat	Method
CGGGGAACTGCGCGAGCAACCCCCACCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_4

>merge|NZ_CP029192|4|4272400-4272511|CRISPRCasFinder
CGGGGAACTGCGCGAGCAACCCCCACCGGCCCGCACGGGGCGTCCCCTCATAGGCGCCGGATGGGGGGGACTACCCAGGGGCGCGGGGAACTGCGCGAGCAACCCCCGCCGG

>NZ_CP029192|4|3|4272400-4272511|CRISPRCasFinder
CGGGGAACTGCGCGAGCAACCCCCACCGG	CCCGCACGGGGCGTCCCCTCATAGGCGCCGGATGGGGGGGACTACCCAGGGGCG
CGGGGAACTGCGCGAGCAACCCCCGCCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150217240.1\|4266001_4266667_-\|deaminase	unknown	unknown	gnl\|CDD\|223340
NZ_CP029192.1\|WP_150170232.1\|4276019_4276667_-\|DUF4956-domain-containing-protein	unknown	unknown	gnl\|CDD\|379819
NZ_CP029192.1\|WP_150221252.1\|4262768_4263065_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217250.1\|4277473_4277953_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|378956
NZ_CP029192.1\|WP_150217252.1\|4279023_4279545_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217243.1\|4269905_4270601_-\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224715
NZ_CP029192.1\|WP_150217241.1\|4266749_4267400_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217237.1\|4263253_4263913_-\|DUF5063-domain-containing-protein	unknown	unknown	gnl\|CDD\|374737
NZ_CP029192.1\|WP_150217244.1\|4270731_4272087_-\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|235687
NZ_CP029192.1\|WP_150217248.1\|4275216_4276023_-\|VTC-domain-containing-protein	unknown	unknown	gnl\|CDD\|143622
NZ_CP029192.1\|WP_150217247.1\|4273904_4275278_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP029192.1\|WP_150217242.1\|4267500_4269909_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133031
NZ_CP029192.1\|WP_150217253.1\|4279847_4281719_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP029192.1\|WP_150217245.1\|4272533_4273052_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370924
NZ_CP029192.1\|WP_150217239.1\|4265164_4265950_+\|SLATT-domain-containing-protein	unknown	unknown	gnl\|CDD\|375613
NZ_CP029192.1\|WP_150217238.1\|4264577_4264922_-\|YbaB/EbfC-family-nucleoid-associated-protein	unknown	unknown	gnl\|CDD\|234669
NZ_CP029192.1\|WP_150217251.1\|4278080_4278842_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376540
NZ_CP029192.1\|WP_055569715.1\|4263905_4264505_-\|recombination-protein-RecR	unknown	unknown	gnl\|CDD\|234616
NZ_CP029192.1\|WP_150217246.1\|4273125_4273905_+\|response-regulator	unknown	unknown	gnl\|CDD\|223816
NZ_CP029192.1\|WP_150217249.1\|4276853_4277459_+\|glutamine-amidotransferase	unknown	unknown	gnl\|CDD\|153234

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150217240.1\|4266001_4266667_-\|deaminase	gnl\|CDD\|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	1.60507e-09
NZ_CP029192.1\|WP_150170232.1\|4276019_4276667_-\|DUF4956-domain-containing-protein	gnl\|CDD\|379819	pfam16316, DUF4956, Domain of unknown function (DUF4956). This family consists of uncharacterized proteins around 220 residues in length and is mainly found in various Bacteroides species. The function of this protein is unknown.	4.78232e-60
NZ_CP029192.1\|WP_150217250.1\|4277473_4277953_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|378956	pfam12802, MarR_2, MarR family. The Mar proteins are involved in the multiple antibiotic resistance, a non-specific resistance system. The expression of the mar operon is controlled by a repressor, MarR. A large number of compounds induce transcription of the mar operon. This is thought to be due to the compound binding to MarR, and the resulting complex stops MarR binding to the DNA. With the MarR repression lost, transcription of the operon proceeds. The structure of MarR is known and shows MarR as a dimer with each subunit containing a winged-helix DNA binding motif.	1.28056e-11
NZ_CP029192.1\|WP_150217243.1\|4269905_4270601_-\|GntR-family-transcriptional-regulator	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	1.97977e-29
NZ_CP029192.1\|WP_150217237.1\|4263253_4263913_-\|DUF5063-domain-containing-protein	gnl\|CDD\|374737	pfam16702, DUF5063, Domain of unknown function (DUF5063).	3.64884e-53
NZ_CP029192.1\|WP_150217244.1\|4270731_4272087_-\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|235687	PRK06062, PRK06062, hypothetical protein; Provisional.	0
NZ_CP029192.1\|WP_150217248.1\|4275216_4276023_-\|VTC-domain-containing-protein	gnl\|CDD\|143622	cd07750, PolyPPase_VTC_like, Polyphosphate(polyP) polymerase domain of yeast vacuolar transport chaperone (VTC) proteins VTC-2, -3 and- 4, and similar proteins. Saccharomyces cerevisiae VTC-1, -2, -3, and -4 comprise the membrane-integral VTC complex. VTC-2, -3, and -4 contain polyP polymerase domains. For S. cerevisiae VTC4 it has been shown that this domain generates polyP from ATP by a phosphotransfer reaction releasing ADP. This activity is metal ion-dependent. The ATP gamma phosphate may be cleaved and then transferred to an acceptor phosphate to form polyP. PolyP is ubiquitous. In prokaryotes, it is a store of phosphate and energy. In eukaryotes, polyPs have roles in bone calcification, and osmoregulation, and in phosphate transport in the symbiosis of mycorrhizal fungi and plants. This subgroup belongs to the CYTH/triphosphate tunnel metalloenzyme (TTM)-like superfamily, whose enzymes have a unique active site located within an eight-stranded beta barrel.	3.97904e-34
NZ_CP029192.1\|WP_150217247.1\|4273904_4275278_+\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.17088e-30
NZ_CP029192.1\|WP_150217242.1\|4267500_4269909_-\|glycosyltransferase	gnl\|CDD\|133031	cd04188, DPG_synthase, DPG_synthase is involved in protein N-linked glycosylation. UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate.	2.58241e-88
NZ_CP029192.1\|WP_150217253.1\|4279847_4281719_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.05387e-78
NZ_CP029192.1\|WP_150217245.1\|4272533_4273052_-\|hypothetical-protein	gnl\|CDD\|370924	pfam10254, Pacs-1, PACS-1 cytosolic sorting protein. PACS-1 is a cytosolic sorting protein that directs the localization of membrane proteins in the trans-Golgi network (TGN)/endosomal system. PACS-1 connects the clathrin adaptor AP-1 to acidic cluster sorting motifs contained in the cytoplasmic domain of cargo proteins such as furin, the cation-independent mannose-6-phosphate receptor and in viral proteins such as human immunodeficiency virus type 1 Nef.	0.00324567
NZ_CP029192.1\|WP_150217239.1\|4265164_4265950_+\|SLATT-domain-containing-protein	gnl\|CDD\|375613	pfam18183, SLATT_2, SMODS and SLOG-associating 2TM effector domain 2. The SLATT domain contains two transmembrane helices. SLATT domains are generally predicted to function as pore-forming effectors in a class of conflict systems which are reliant on the production of second messenger nucleotide or nucleotide derivatives. SLATT domains are predicted to initiate cell suicide responses upon their activation. This SLATT family is the only prokaryotic SLATT family to exist as a standalone domain, with no as-yet discernable genome associations.	1.00067e-114
NZ_CP029192.1\|WP_150217238.1\|4264577_4264922_-\|YbaB/EbfC-family-nucleoid-associated-protein	gnl\|CDD\|234669	PRK00153, PRK00153, YbaB/EbfC family nucleoid-associated protein.	6.31677e-39
NZ_CP029192.1\|WP_150217251.1\|4278080_4278842_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|376540	pfam01381, HTH_3, Helix-turn-helix. This large family of DNA binding helix-turn helix proteins includes Cro and CI. Within Neisseria gonorrhoeae NGO_0477, the full protein fold incorporates a helix-turn-helix motif, but the function of this member is unlikely to be that of a DNA-binding regulator, the function of most other members, so is not necessarily characteristic of the whole family.	0.000543997
NZ_CP029192.1\|WP_055569715.1\|4263905_4264505_-\|recombination-protein-RecR	gnl\|CDD\|234616	PRK00076, recR, recombination protein RecR; Reviewed.	6.69424e-125
NZ_CP029192.1\|WP_150217246.1\|4273125_4273905_+\|response-regulator	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.49777e-78
NZ_CP029192.1\|WP_150217249.1\|4276853_4277459_+\|glutamine-amidotransferase	gnl\|CDD\|153234	cd03140, GATase1_PfpI_3, Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. PfpI is an ATP-independent intracellular proteases which may hydrolyze small peptides to provide a nutritional source. Only Cys of the catalytic triad typical of GATase1 domains is conserved in this group. This Cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow.	3.44054e-63

>NZ_CP029192.1|WP_150217244.1|4270731_4272087_-|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme
MTPQPNPQVGAAVKAADRAHVFHSWSAQELIDPPAIAGAEGAYFWDYDGNRYLDFTSGLVYTNIGYQHPKVVAAIQEQAATMTTFAPAFAVEARSEAARLIAERTPGDLDKIFFTNAGADAVEHATRMARLHTGRPKVLAAYRGYHGGTHQAINLTGDPRRWASDTGTAGVVRFWAPFLYRSRFYAETEAQECERALQHLEDTIVFEGPQTIAAIILETVPGTAGIMIPPPGYLAGVRALCDKYGIVFILDEVMAGFGRTGEWFAADLFDVTPDLLTFAKGVNSGYVPLGGVAISGEIAETFARRPYPGGLTYSGHPLACAAAVATINVMAEEGIVDHAADLGARVIEPGLRALAERHPSVGEVRGVGMFWALELVKDRETREPLVPYNATGEANAPMAAFGAAAKKQGLWPFINMNRTHVVPACNITETEAKEGLAALDVALSVADEHTV
>NZ_CP029192.1|WP_150217243.1|4269905_4270601_-|GntR-family-transcriptional-regulator
MPGTDGPAVIRSTLRQQIADALRDEVLAGRLEPGQEFTVKEIAEQYGVSATPVREALVNLTAQGLLDADQHRGFRVHEHTLDDYRGMLEARGLIADGIFRDLVAHRARRDTADALFSVRRRGEEAARAACAGDLTVLIGYDLRFWRELSALFGNAYLSDFLHRLRVKSWVCAVTHLRRWSDINGGDLRGLLWSRHTELVDALVRDDPEAAHGIVREYNAHSLALIERLAAA
>NZ_CP029192.1|WP_150217242.1|4267500_4269909_-|glycosyltransferase
MSVDLSVVVPAYNEEQRLGPTLDALRDHLETTCRGAWELIVVDDGSTDRTAEIAAEASAADPRVQLVRGDRNRGKGHALRLGVLASYGSRVLVTDADLAAPIEELDHLDKALTDGHAAAIGSRARPGATIDTHQHRLRELLGRTGNFLIRSVAVPGIRDTQCGFKLFDGDRAREAFAASRLHGWGIDVEILQYFRRAGWPVAEVPVRWSHQEGSKVRPLDYVKVLAELTTLKARTVRRADVVVALLFLALSVFLYSSRWVAPAHRYIPDSLQDQNQWEWFFAVTADNVRHLNNPLFTTLQNVPDGVNLMANTVMLGLSVPLAPVTWLLGPAVALNVAMTGGLAATAVSWYALIRRRLVPHRGAAAVGAAVAAFAPPMVSHANAHPNFIVLFMIPLIIERALRLCEGTRVVRNGVVLGLYTTYQIFLGEEPLLLAALGMLLFALAYAAVRRDVARAAWRPLARGLAIALAVTIPLVAFPLHWQFFGPQSYQSVLHGDNVGNSPLAFFSFAERSLAGSHETADHLAMNPTEQNAFFGWPLAALAFAIVVRLWERTVVKALAFTVLAAALLSLGPKFRIPLTDVVLPGPWAALSGRPLFESVIESRVAMVCAPALGMLLALALVQLLRAPRRAHRFAGVAAVALALLPVFPAPLKAVDRVDVPPFIAQGTWRTYLGEGETLVPVPVPDPANAEGLHWQVDADLGFRIPGGYFNGPWGPDRVGIYGPSPRNTSNLLRDVRSSGRVPEVTPAWREAVRQDLEFWKAGLLVLAPQQNDGELRTTVDALLGRPGKWVDGVWIWDLRKGS
>NZ_CP029192.1|WP_150217241.1|4266749_4267400_-|hypothetical-protein
MACDLWLVPLVDVLCHSADNPFAEELAVYDKALHEAGFPPVPVFAYMPGLSGDVAPVAGFDYDALHFLRRAYLLQICGLEVTPVDELGGDYEQLLEMFDATAQQSHLVWHYDHAGAYVPVDFPAPLSNEELLAGGGPLGSSHALLRELEYVAPSIGIDAANPPLAPAPPSAPTSLEEPAAPSPPDASPFARERHVWLGLHAAATRSLAQGSMIIYS
>NZ_CP029192.1|WP_150217240.1|4266001_4266667_-|deaminase
MSRQQERQQLLKVQNFMLSQDGFGTGEGQSLERPFGHADPREMSAWAVATASWPNRTDPGGTRGLDDYFTRDFSHNIGAEIMGRNKFGPQRGPWQDHEWRGWWGDEPPFHTPVFVMTHHERPSFTLSDTTFHFVAGDPATVLERAKEAAQGKDVRLGGGPTIVREFLEAGLVDTLHVAVVGQMKLGAGVRLWNSPEDLTDRYHLEVVPSPSGVTHHLFWRR
>NZ_CP029192.1|WP_150217239.1|4265164_4265950_+|SLATT-domain-containing-protein
MSQPEMQPEGVPPETPEGQGSGGSGGTPSGGVPTGDLTGRAFPLGDWGDPAGRLDELYRWVERGALNTAEWYLTDRGRKRRAARLLRVGAALGAVGAGVLPLLDLARAGGAGTTGGLAGWGFVSLLVGVACVGCDRFFGLTSGWMRDVATAQAVQRRLQVLQFDWASESVREVLGPTEGTAGEAAERCLGVLRRFTDDITELVRAETSDWMVEFRAGPVPLAMQAIVPGGAPREAPASPGRFPLPPGARPNMPRQRPPEPR
>NZ_CP029192.1|WP_150217238.1|4264577_4264922_-|YbaB/EbfC-family-nucleoid-associated-protein
MIPGGGQPNMQQLLQQAQKMQQDLAAAQEELARTEVEGQAGGGLVKATVNGSGELRGLVIDPKAVDPEDTETLADLVVAAVQAANENAQALQQEKLGPLAQGLGGGGGIPGLPF
>NZ_CP029192.1|WP_055569715.1|4263905_4264505_-|recombination-protein-RecR
MYEGVVQDLIDELGRLPGVGPKSAQRIAFHILQAEPTDVRRLAHALLEVKDKVRFCATCGNVAQEELCNICRDPRRDPSVICVVEEPKDVVAIERTREFRGKYHVLGGAISPIEGVGPDDLRIRELLARLADGTVTELILATDPNLEGEATATYLARMIKPMGLKVTRLASGLPVGGDLEYADEVTLGRAFEGRRLLDV
>NZ_CP029192.1|WP_150217237.1|4263253_4263913_-|DUF5063-domain-containing-protein
MSDATLNTVTDNPDDFAVQISDQIESFIVSVREVAKGDEPDSAVPFLLLEVSQLLLAGGRLGAHEDIVPEERYEPDLGPEQDVDDLRERLASLLDPIDVYSEVFDPYEPRKAPVPCRISDDLADVVADLSHGLAHYRAGRTTEALWWWQFSYFSNWGSTASGALRALQSLVAHVRLNQPLDDLDGLDTDEDLGADGLEEEAGKVMAEEIAGPLGLRTIK
>NZ_CP029192.1|WP_150221252.1|4262768_4263065_-|hypothetical-protein
MGLAEAIGAVRAELRRAAEEGRGQDLQFRTGPVELEFTVDVRKDAEARAKVLVLPFGAEAKASRSKGTVNRLKVTLQPVDPSTGEDARVGDDVDERPR
>NZ_CP029192.1|WP_150217245.1|4272533_4273052_-|hypothetical-protein
MRKWRNAVVTAAWVAVGTAAGALGAWQLASADSDGAGGAAHSRPLDEAAVRRALAASDPPPTSRSTPTPPSPPPSRSLTPPASSPPSAERSTVRFTGGSATVECRADGTVRLVSWSPADGFHIDDDVERGPAAVARLEAEPGDDDEQPDLPYEIRCVGGTPRAQVVPDTDDD
>NZ_CP029192.1|WP_150217246.1|4273125_4273905_+|response-regulator
MAHLLVVEDDPQLRGALVRALRDKGHAVATAPSGMAGLDAAVTSGPDLVVLDLGLPDVDGAQVLRMLRAVSDVPVIVATARDDEPGMVTVLEAGADDYIVKPFGAAQLDARIKAVLRRLGVTETEEPLRVGGLSIDPASREVTLDEAALDLTPREFDLLAYLARRPGQVVSRRELLAEVWQQPLGGADKTVDVHLSWLRRKLGETAQRPRYLHTVRTVGVKLAAPDGQGHSEEEPSEQGADQRAHGEHGPNENEQGGPA
>NZ_CP029192.1|WP_150217247.1|4273904_4275278_+|HAMP-domain-containing-protein
MRRSLLLLTAATTALVLTALLVPLTLLTRSHAADRATAEATARAQWVAHALGPALATTDERETAEQTVESVNGKDLPSTSLILADGKVIGPRLGHGSAVTDPVRLARTGRAFTYETSSGGRLVLVPVQGAKDGTAVVQVTLSERQLYAGTLASWLVLVGIGVGLVLVGLLLADRLGARLVGATRRLARTADRLAAGDLTARAEPEGPPELRLIAGELNRLASRIDELLTAERENAADLAHRLRTPVAALRLDAETLRDPDEAHRIAADVLALERSVNDVIRKARRPLREAPRADLAAVARERTAFWAPLAEDQNRTVHTTTPDDGEVPVPVPADELTAALDALIGNVLDHTPHGTAFSLTVRRTSEGRAAELTVADEGPGFPDPGAAPDRGRSGAGSTGLGLDIARRTAEEAGGTFETATATPREGGARVTLTFPLPLTPPRAHPAGTPSAPPAPTC
>NZ_CP029192.1|WP_150217248.1|4275216_4276023_-|VTC-domain-containing-protein
MNPAVRAIGRAATAAHPIALDEVNARAELLARFDNSYLVPVEIFEDLAALLTDPRRSGGPFRALSIGGKRWFRYHSTYYDTPDLGTFHDHRQGRRLRYRIRERVYRDSGERQFEIKLKSGRGETVKHRQRLEGDDHALDAVRLGFLDGVLRGSYGIEAPDGLTPSLVTDYQRATFVADGQRITCDAGLVVRDTATGRSAAADSGLVLVETKTKGHLTDADRVLHRYGVRAADFTKYCGGYAAVRPELGINKWARAVRTAFPRGARAGV
>NZ_CP029192.1|WP_150170232.1|4276019_4276667_-|DUF4956-domain-containing-protein
MDSTLTLCAHLGLDLAAVALLTFGVFYPRHRRRELVPAYLALNVALFAIVAGLGTVGGDGGLALGFGLFGVLSIVRLRSDALQHQEVAYYFITLVLGLLCGLPALGLPVAALLAGVLLVVMYGADHPRLFARDRRTVVTLDSVHREEESLRAELARRLGEPLGWTVQEVDYVRDLMVLEVRFRQPEPSVTSRELTVRRRTTRSRTIAPSHPKETV
>NZ_CP029192.1|WP_150217249.1|4276853_4277459_+|glutamine-amidotransferase
MSLTSRKPVHLALYDTFADWETGHATAWLARFGYEIRTVAPSAEPVVSIGGLRVQPDLSLAELRPEDSSLLILPGADLWDTSDDLAPFAHTARAFLDAGVPVGAICGATAGLAREGLLDDRTHTSGASMYLAATGYKGGERYAEKDAVTDGDLITAGPTEPVAFAREIFARLGDVLDAEKLDAWYRLFHDSDPAAYETLNS
>NZ_CP029192.1|WP_150217250.1|4277473_4277953_+|MarR-family-transcriptional-regulator
MPAPHTPQDLLTRTALTVFRLNGQFLTVSEELAKPAGLTAAWWQVLGAVLRDPLPVAGIARTMGITRQSVQRVADLLVREGLAEYAPNPAHRRAKLLRPTAEGRAAVAHIDPGHARLAARLADALGETEFAETARVLERLATVLDDVVDADARTGTSEA
>NZ_CP029192.1|WP_150217251.1|4278080_4278842_-|helix-turn-helix-transcriptional-regulator
MATPNGTLQAVRKGLLMSQDEFARAVRDAGQQLGQPNEASKRLVQRWESGDTAAPRQLYARALERVTGVPIEALGFGVPSVAVTEDGRGGHDLDDATFSVTAGQSAPAPSAAPRGNFTGVWLSTYEYVSSGRDDAVFIGKHHVVLLQHGNRLTGRSLPNGSLNPASPLTLDLQVEGATVTGTWAEQTASDGYYRGARYFGALQLLAEPTGRRMVGKWVGFGKEFDVNTGPWELRLMDSATSKAALAQYDRAPE
>NZ_CP029192.1|WP_150217252.1|4279023_4279545_+|hypothetical-protein
MAGFTGRALSVAAVDSPGLVSAAFDWLARAQDEPRKARLEWAEQGIALLPLGTRFNSVCLPASLVYEAVGTGDLNTVAATLAELLGGPVIHNRVQHRYHALVECSPTQRWMREYSEAPMLGIGHHLSVPASDLRGPTGLYWAVRPRIVGGLCPVRSVATLVHIARSESRRGPQ
>NZ_CP029192.1|WP_150217253.1|4279847_4281719_+|protein-kinase
MEKLVPGDPQRIGAYRLLARLGAGGMGQVYLARSERGRTVAVKLVREELAEQDEFRNRFRQEVQAARQVGGAWTAPVLDADTEAAIPWLATGYVAGPSLQAVVSHDHGPLPERSVNILGAGLAHALKDIHAAGMVHRDLKPSNVLVTIDGPRVIDFGIARALETVTDGGLTRTGALVGSPGFMAPEQVRGDRITPACDVFCLGSVLAYAASGALPFGTANSGVHALMFRIAQEEPDLEELPEGLTELIAACLRKEPGDRPSLDEVLERTGAADALGDGHTLDPWLPGALVAQLGRHAVQLLDAEDPEEAAAQEAGEGAEVGAGAGSGAARDATPPPPGKPGTAPLDHLPTMVSGGSGSGSGGGGQAPPAPAPTPTPAPPPGAPVYGYPHQPPHQPAGYGYPQYPHQHPQAAPPGFGPTPPYGPVPPPEPARRSGRSTAALVVVALIVALGAGGTVYAVMNGDSADDKQRDDSANGTGASSAPKTPGSATPSPESSGPEPSPSDSDDGTVPDKYLGTWSGGLDTANGHSTRELTLQQGGVGDTVLSVTADGPADGGGTYHCVFQGKLVSASGERLRIGPTEVTVGEPMTSCTPGDPSVITVLGNGKLRRANTDGSGELTYEKGN

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_CP029192_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_5

4523282-4523422

Orphan

Consensus_repeat	Method
CCGGCGGCGGTCAGCAGCAGGGTGGCGGCGGTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_5

>merge|NZ_CP029192|5|4523282-4523422|CRISPRCasFinder
GCGGTGGCGGCGGCCAGCAGGGCGGCGGCTGGGGCGGTGGCTCCGGCGGCGGTCAGCAGCAGGGTGGCGGCGGTGCTCCCGCCGACGACCCCTGGGCGACCGGTGCGCCGGCCGGCGGCGGTCAGCAGCAGGGCGGCGGCG

>NZ_CP029192|5|4|4523282-4523422|CRISPRCasFinder
GCGGTGGCGGCGGCCAGCAGGGCGGCGGCTGGG	GCGGTGGCTCCGGCGGCGGTCAGCAGCAGGGTGGCGGCGGTGCTCCCGCCGACGACCCCTGGGCGACCGGTGCGC
CGGCCGGCGGCGGTCAGCAGCAGGGCGGCGGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150217451.1\|4531981_4532446_+\|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl\|CDD\|225039
NZ_CP029192.1\|WP_016644628.1\|4522521_4522812_+\|30S-ribosomal-protein-S6	unknown	unknown	gnl\|CDD\|179034
NZ_CP029192.1\|WP_055565790.1\|4520671_4521793_-\|peptidoglycan-bridge-formation-glycyltransferase-FemA/FemB-family-protein	unknown	unknown	gnl\|CDD\|225224
NZ_CP029192.1\|WP_150217440.1\|4519573_4520605_-\|alanine-racemase	unknown	unknown	gnl\|CDD\|376473
NZ_CP029192.1\|WP_150217447.1\|4528763_4529675_-\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176191
NZ_CP029192.1\|WP_150217450.1\|4531438_4531918_+\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133384
NZ_CP029192.1\|WP_150217437.1\|4513994_4514681_-\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_CP029192.1\|WP_150217448.1\|4529746_4530379_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP029192.1\|WP_150217441.1\|4521940_4522255_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217449.1\|4530414_4531368_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235736
NZ_CP029192.1\|WP_003949403.1\|4523561_4523798_+\|30S-ribosomal-protein-S18	unknown	unknown	gnl\|CDD\|178997
NZ_CP029192.1\|WP_150217434.1\|4510877_4511402_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223021
NZ_CP029192.1\|WP_150217444.1\|4524453_4525791_-\|MATE-family-efflux-transporter	unknown	unknown	gnl\|CDD\|240541
NZ_CP029192.1\|WP_150217439.1\|4517957_4519484_+\|DUF2029-domain-containing-protein	unknown	unknown	gnl\|CDD\|227937
NZ_CP029192.1\|WP_150217436.1\|4512852_4513935_-\|inositol-3-phosphate-synthase	unknown	unknown	gnl\|CDD\|132491
NZ_CP029192.1\|WP_150217443.1\|4523816_4524263_+\|50S-ribosomal-protein-L9	unknown	unknown	gnl\|CDD\|234659
NZ_CP029192.1\|WP_150217438.1\|4515054_4517820_+\|penicillin-binding-protein	unknown	unknown	gnl\|CDD\|223815
NZ_CP029192.1\|WP_150217445.1\|4526251_4527733_+\|replicative-DNA-helicase	unknown	unknown	gnl\|CDD\|273206
NZ_CP029192.1\|WP_150217446.1\|4527784_4528702_-\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176191
NZ_CP029192.1\|WP_150217435.1\|4511516_4512773_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340863

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150217451.1\|4531981_4532446_+\|carboxymuconolactone-decarboxylase-family-protein	gnl\|CDD\|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	2.28766e-15
NZ_CP029192.1\|WP_016644628.1\|4522521_4522812_+\|30S-ribosomal-protein-S6	gnl\|CDD\|179034	PRK00453, rpsF, 30S ribosomal protein S6; Reviewed.	3.10898e-39
NZ_CP029192.1\|WP_055565790.1\|4520671_4521793_-\|peptidoglycan-bridge-formation-glycyltransferase-FemA/FemB-family-protein	gnl\|CDD\|225224	COG2348, COG2348, Peptidoglycan interpeptide bridge formation enzyme [Cell wall/membrane/envelope biogenesis].	4.62093e-32
NZ_CP029192.1\|WP_150217440.1\|4519573_4520605_-\|alanine-racemase	gnl\|CDD\|376473	pfam01168, Ala_racemase_N, Alanine racemase, N-terminal domain.	3.35916e-09
NZ_CP029192.1\|WP_150217447.1\|4528763_4529675_-\|zinc-binding-dehydrogenase	gnl\|CDD\|176191	cd05289, MDR_like_2, alcohol dehydrogenase and quinone reductase-like medium chain degydrogenases/reductases. Members identified as zinc-dependent alcohol dehydrogenases and quinone oxidoreductase. QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR actin the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	3.9834e-92
NZ_CP029192.1\|WP_150217450.1\|4531438_4531918_+\|MerR-family-transcriptional-regulator	gnl\|CDD\|133384	cd01109, HTH_YyaN, Helix-Turn-Helix DNA binding domain of the MerR-like transcription regulators YyaN and YraB. Putative helix-turn-helix (HTH) MerR-like transcription regulators of Bacillus subtilis, YyaN and YraB, and related proteins; N-terminal domain. Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	1.29079e-41
NZ_CP029192.1\|WP_150217437.1\|4513994_4514681_-\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.79151e-19
NZ_CP029192.1\|WP_150217448.1\|4529746_4530379_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	2.09608e-12
NZ_CP029192.1\|WP_150217435.1\|4511516_4512773_-\|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.	5.92825e-39
NZ_CP029192.1\|WP_003949403.1\|4523561_4523798_+\|30S-ribosomal-protein-S18	gnl\|CDD\|178997	PRK00391, rpsR, 30S ribosomal protein S18; Reviewed.	9.24137e-38
NZ_CP029192.1\|WP_150217434.1\|4510877_4511402_-\|hypothetical-protein	gnl\|CDD\|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	9.02762e-05
NZ_CP029192.1\|WP_150217444.1\|4524453_4525791_-\|MATE-family-efflux-transporter	gnl\|CDD\|240541	cd13136, MATE_DinF_like, DinF and similar proteins, a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Escherichia coli DinF is a membrane protein that has been found to protect cells against oxidative stress and bile salts. The expression of DinF is regulated as part of the SOS system. It may act by detoxifying oxidizing molecules that have the potential to damage DNA. Some member of this family have been reported to enhance the virulence of plant pathogenic bacteria by enhancing their ability to grow in the presence of toxic compounds. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	3.68466e-114
NZ_CP029192.1\|WP_150217439.1\|4517957_4519484_+\|DUF2029-domain-containing-protein	gnl\|CDD\|227937	COG5650, COG5650, Predicted integral membrane protein [Function unknown].	1.82936e-37
NZ_CP029192.1\|WP_150217436.1\|4512852_4513935_-\|inositol-3-phosphate-synthase	gnl\|CDD\|132491	TIGR03450, mycothiol_INO1, inositol 1-phosphate synthase, Actinobacterial type. This enzyme, inositol 1-phosphate synthase as found in Actinobacteria, produces an essential precursor for several different products, including mycothiol, which is a glutathione analog, and phosphatidylinositol, which is a phospholipid.	0
NZ_CP029192.1\|WP_150217443.1\|4523816_4524263_+\|50S-ribosomal-protein-L9	gnl\|CDD\|234659	PRK00137, rplI, 50S ribosomal protein L9; Reviewed.	7.03641e-65
NZ_CP029192.1\|WP_150217438.1\|4515054_4517820_+\|penicillin-binding-protein	gnl\|CDD\|223815	COG0744, MrcB, Membrane carboxypeptidase (penicillin-binding protein) [Cell envelope biogenesis, outer membrane].	8.71449e-142
NZ_CP029192.1\|WP_150217445.1\|4526251_4527733_+\|replicative-DNA-helicase	gnl\|CDD\|273206	TIGR00665, DnaB, replicative DNA helicase. This model describes the helicase DnaB, a homohexameric protein required for DNA replication. The homohexamer can form a ring around a single strand of DNA near a replication fork. An intein of > 400 residues is found at a conserved location in DnaB of Synechocystis PCC6803, Rhodothermus marinus (both experimentally confirmed), and Mycobacterium tuberculosis. The intein removes itself by a self-splicing reaction. The seed alignment contains inteins so that the model built from the seed alignment will model a low cost at common intein insertion sites. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP029192.1\|WP_150217446.1\|4527784_4528702_-\|zinc-binding-dehydrogenase	gnl\|CDD\|176191	cd05289, MDR_like_2, alcohol dehydrogenase and quinone reductase-like medium chain degydrogenases/reductases. Members identified as zinc-dependent alcohol dehydrogenases and quinone oxidoreductase. QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR actin the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	4.3064e-85
NZ_CP029192.1\|WP_150217449.1\|4530414_4531368_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|235736	PRK06196, PRK06196, oxidoreductase; Provisional.	2.731e-168

>NZ_CP029192.1|WP_016644628.1|4522521_4522812_+|30S-ribosomal-protein-S6
MRHYEVMVILDPDLEERAVSPLIENFLSVVREGNGKVEKVDTWGRRRLSYEIKKKPEGIYSVIDLQAEPAVVKELDRQMNLNESVLRTKVLRPEMH
>NZ_CP029192.1|WP_150217441.1|4521940_4522255_-|hypothetical-protein
MAQAMRPNSATSLFATDGKAHPLQDTLLGVTLVLGAIAFVTAMFHNLHLISSWTGLAGIATGAYGQFISVTTRERFGLILGLGASAVGFFLGMAHGGLFGGVVG
>NZ_CP029192.1|WP_055565790.1|4520671_4521793_-|peptidoglycan-bridge-formation-glycyltransferase-FemA/FemB-family-protein
MSLTLRTISREQHLAYIQTLPSASHCQVPAWADVKSEWRSENLGWFDDRTGELVGAGLVLYRQLPKLKRYLAYLPEGPVINWYAPNLDEWLQPMLAHLKQQGAFSVKMGPPVVIRRWDAPAIKAGIQNPDVKRLRDTEATYIEPRAFEVSDRLRRMGWQQGEDGGAGFGDVQPRFVFQVPLANRSLDEVQKGFNQLWRRNIKKAEKAGVEVVQGGYHDLPEWQRLYEITAVRDKFRPRPLGYFQQMWQALNSEDPNRMRLYFARHNGVNLSAATMLVVGGHVWYSYGASDNIGREVRPSNAMQWRMLRDAYAMGATVYDLRGISDSLDETDHLFGLIQFKVGTGGEAAEYIGEWDFPLNKLLHKALDIYMSRR
>NZ_CP029192.1|WP_150217440.1|4519573_4520605_-|alanine-racemase
MALTLYVDTARWRAHQKHMLEQFPGIVPVCKGNGYGFGHERLAEEATRFGSDVLAVGTTYEAARIKDWFSGDLLVLTPFRRGEEPVPLPDRVIRSVSSLDGVHGLVGARVVIEVMSSMKRHGVSEQELPQLHAAIEDVRLEGFAIHLPLDRTDGSDAVEEVIGWMDRLRAARLPLHTMFVSHLKAGELARLQQQFPQTRFRARIGTKLWLGDHEATEYRGAVLDVTAVAKGDRFGYRQQKAASDGWLVVVAGGTSHGVGLEAPKALHGMMPRAKGVARAGLATVNRNLSPFVWAGKQRWFAEPPHMQVSILFVPSDAPEPKVGEELVAHLRHTTTQFDRIIDR
>NZ_CP029192.1|WP_150217439.1|4517957_4519484_+|DUF2029-domain-containing-protein
MPSADPSAETPRTSAYEPVSPQEQEPVRPTREDEVARSGSELMGGPVGRRVLFAASWWTPVRIIALVALGMFALGMVQKMPCYNGAWFLGASSQYTHACYSDIPHLYQGRGFADGLVPYFDRLPGDMEYLEYPVLTGVFMEMASWVTPGSGSIQHQEKIYWMVNAGILMACTAVVAVCVARTHRRRPWDGLLVALAPAFALTATINWDLLAVALTAAAMLMWSRSRPVAFGVLLGLATAAKLYPVLILGPLLILCWRAGRWRAFGTALLGTVSAWLVVNLPVMLLASDGWSKFYTFSQERGVDFGSFWLILSQRMDSPLSTDTVNTLATALMLVACLGVGALGLTAPRRPRFAQLAFLVVAAFILTNKVYSPQYVLWLIPLAALARPRWRDFLIWQACEVAYFLGIWLYLAYTTSGDAHKGLPTEGYQLAIVVHLLGTLYLCAVVVRDVLMPERDVVRSSGDDDPSGGVLDGSRDVFVLGTARYAGRAALHTAQAPTVKWGSAADAPR
>NZ_CP029192.1|WP_150217438.1|4515054_4517820_+|penicillin-binding-protein
MSEHRRKPPQPQGGGRAAARRGTPGAPSGRRAAPRGDTGSPSASYGGPGPGSGAPDDGDRPYGGRAEARRAAQRSGSVGAGGGRRRAPDGGGRAGGGGGRRGGGSGGSSGPGRGRGRGAEPPRKKRFIDYPRAGKSGARRWVPSWRLVTGVFLGFFGGLMAVAGISYALVEVPEVDKAAKAQNNVYYWADGKQMVATGGERNRQIIDYDDIPKEMRFAVMSAENKTFEKDKGVDPMGITRAVVNMAKGGQTQGGSTITQQYVKNARLGDQSQTFTRKFKELFISIKVGRTVSKEDIMAGYLNTAYYGRGAYGIQAAARAYFNEEASKLDPSQCAFLATVLKGATYYDPAGYPEIDPAANKQDNTARAKKRWAWILDEEVKDGRLTSEQRAQFTKFPKLQNPRSNMDLAGQTGYLVDLAKAYVIRNTNITAEQLQRGGYEIHTTFERRKVNELEKAVNKVRKEKIKPKVRPEKDTHVQFGGASVDPKTGAIKAIYGGEDATKHFTNNADQTGAQVGSTYKPFVLAAAFKYGVRDPDGPEEQSEAERTIVNPKSLYSGKNELKIQKYNGQIWTDRDGKQWNQKNDGNQSYNRPSFQIDLREAMRESVNSAYVQLGMDVGLEKVKQAAMEAGLKDDSSMAGATYPSFSLGTSSPSAIRMAGAYSTFAASGKQNEPYSVSEVEHEGDTVFRHEKETKQAFSAEVADNVTDVLRTVVEKGTGTSAKLTGRQVAGKTGTTDGNKSAWFVGYTPQLSTAVSMYRLDDDETNKKRKFLEMFGTGGEEKIHGASFPAQIWQDYMEQALKGKSVVNFPVPGPIGKVVGETPPPPPTPTKTEEPEETTSPTPTETEPSKPPTHSPDPTDTCDPFDWDCNHDGGQQNGGADGGVDGGPGGESPPPTEDPVGGGGSNGNGNGNGGGGIFGGPSD
>NZ_CP029192.1|WP_150217437.1|4513994_4514681_-|PadR-family-transcriptional-regulator
MSRRSGILEFAVLGLLRESPMHGYELRKRLNTSLGVFRAFSYGTLYPCLKTLVANGWLIEESGGTPEDALAAPLAGRRAKIVYRLTAEGKEHFEDLLSQTGPDAYEDEHFAARFAFFGQTSRDVRMRVLEGRRSRLEERLEKMRASLARTRERLDDYTLELQRHGMESVEREVRWLNELIESERAGRDQQRSAPGSSAQQNSTSGESAGLPRRRENDPPPDPSDDPAK
>NZ_CP029192.1|WP_150217436.1|4512852_4513935_-|inositol-3-phosphate-synthase
MGSVRVAIVGVGNCAASLVQGVEFYKDADPDTKVPGLMHVQFGEYHVGDVEFVAAFDVDAKKVGLDLSDAIGASENNTIKICDVPNSGVTVQRGHTYDGLGKYYRQTIEESDEAPVDVVQILKDRQVDVLVCYLPVGSEDAAKFYAQCAIDAKVAFVNALPVFIAGTKEWADKFTEAGVPIVGDDIKSQVGATITHRVMAKLFEDRGVRLERTMQLNVGGNMDFKNMLERDRLESKKISKTQAVTSQIPDRELGEKNVHIGPSDYVAWLDDRKWAYVRLEGRAFGEVPLNLEYKLEVWDSPNSAGVIIDALRAAKIAKDRGIGGPILSASSYFMKSPPVQYFDDEAYANVEKFIKGEVER
>NZ_CP029192.1|WP_150217435.1|4511516_4512773_-|MFS-transporter
MAVVGDLRILLRLRDFRRLLAVRLISQGADGVYQVALATYVVFSPEKQASPGAIASAMAVLLLPYSLIGPFAGVLLDRWPRRQVFLHGNLLRAALASLTAVLMLSGVPDWLFYASALCVTAVNRFVLAGLSAALPRVVDADRLVIANSLSPTAGTLAATLGGGLAFVIRLAASDSDAAVVLCGATLYLCAALASLRMARELLGPDPDLVQPRLTTALAGTARGLRAGVHHLTQRPAAARALAAMTVLRFCYGALTVMVLMLCRYAWTSTEADGLALLGLAVGISGAGFFVAAVVTPAAVGRLGPGGWIVTCAATAALLEPALGLPFEPVPLLIAAFFLGLTTQGAKIATDTVVQSSVDDGFRGRVFSIYDVLFNIAFVGAAAVAALMLPPDGRSVPLVLVVALLYAAVAGGMGRFGAQ
>NZ_CP029192.1|WP_150217434.1|4510877_4511402_-|hypothetical-protein
MTTPPPQGQTPYPPQGQNPYGQPQGGAAPYGQAPPAPYPPQQGQPGGPTAPYPAFNQGGPVPPPPAPRRGGAKKLLLRIGGFILVAILIAVGKWYMGKSDAESTSVGSCMHNKGTEIRPDLEEVDCSSSDSEFEVVEKFDGTSDSSKCETVKTSEIAYYQSGKGHNVVLCLKKA
>NZ_CP029192.1|WP_003949403.1|4523561_4523798_+|30S-ribosomal-protein-S18
MAKPPVRKPKKKVCAFCKDKVTYVDYKDTNMLRKFISDRGKIRARRVTGNCTQHQRDVATAVKNSREMALLPYTSTAR
>NZ_CP029192.1|WP_150217443.1|4523816_4524263_+|50S-ribosomal-protein-L9
MKIILTHEVSGLGAAGEVVDVKDGYARNYLIPRNFAIRWTKGGEKDVEQIRRARKIHEIATIEQANEIKAQLEGVKVRLAVRSGDAGRLFGSVTPADVASAIEAAGGPKVDKRRVELGSPIKTLGAHTTSVRLHPEVAAKVNVEVVSA
>NZ_CP029192.1|WP_150217444.1|4524453_4525791_-|MATE-family-efflux-transporter
MTQAPAAPKAARRRHDREIIALAVPAFGALVAEPLFVLADSAIVGHLGTAQLAGLGVASALLTTAVSIFVFLAYATTAAVARRVGAGDLQAAIRQGMDGIWLALLLGAAVIAVVLPTAPALVDLFGASDTAAPYAVTYLRISSLGIPAMLVVLAATGVLRGLQDTRTPLYVAIGGFVANGVLNVGLVYGADLGIAGSAWGTVIAQCGMAAVYLYVVVRGAKRHGASLRPDAAGIRACAQAGAPLLVRTLSLRAILMIATAVAARLGDSDVAAHQIVLSLWSLLAFALDAIAIAGQAIIGRYLGADDPDGARAVCRRMVQWGIASGVVLGLLVVLARPVFIPLFTGDGDVQDAALPALVVIALAQPICGIVFVLDGVLMGAGDGPYLAWAMIVTLAAFTPVALLVPTFGGGLTALWGAMTLMMAVRMLTLWLRSRSGRWLVTGATR
>NZ_CP029192.1|WP_150217445.1|4526251_4527733_+|replicative-DNA-helicase
MSISEPLDDPWADSGPSDRLPVSRQRRDGGGGRSRDEQHDRGREGGWDGGGSSFERVPPQDLDAEQSVLGGMLLSKDAIADVVEVLKGHDFYRPAHETIYASILDLYAKGEPADPITVAAELTKRGEITKVGGASYLHTLVQTVPTAANAEYYAEIVHERAVLRRLVEAGTKITQMGYAADGDVDEIVNSAQAEIYAVTEQRTTEDYLPLGDIMEGALDEIEAIGSRSGEMTGVPTGFTDLDQLTNGLHPGQMIIIAARPAMGKSTLALDFARACSIKHNMPSVIFSLEMGRNEIAMRLLSAEARVALHHMRSGTMTDEDWTRLARRMPDVSAAPLYIDDSPNLSMMEIRAKCRRLKQRNDLKLVVIDYLQLMQSGGSKRSESRQQEVSDMSRNLKLLAKELELPVIALSQLNRGPEQRTDKKPMVSDLRESGSIEQDADMVILLHREDAYEKESPRAGEADIIVGKHRNGPTATITVAFQGHYSRFVDMAQT
>NZ_CP029192.1|WP_150217446.1|4527784_4528702_-|zinc-binding-dehydrogenase
MRYHRYGGPEVLCLEEAEEPHAGPGQVRVAVRATGVTPADWYLRSGMLRDIAPLDFPHIPGMDAAGTVDEVGEGVVGTAVGDAVFGLVPFADRGGAAARYAVLEAWAHNPRAWSFEEAGGAAGNVDTATRVLEALEATEGMTLLIEGAAGGVGTVTAQLARARGLSVIGTASEGNHGFLDRLGVVPVTYGPGLAERVAPLAPHGIDVVLDAAGKGSLAELVAITGDPRRVITIADFDADRHGVRFSRSEAGASPGWAGLPLAARLADQGQLTIPLHAVFALKETASAHEASAAGHARGKIVITVP
>NZ_CP029192.1|WP_150217447.1|4528763_4529675_-|zinc-binding-dehydrogenase
MKRVSFAEYGGPDVLHLTEAEEPHAGPGQIRVAVRAAGVNPVDWRIREGQFRQAQQFPQTHFSELPSGTGQDAAGVVDEVGPDVTTVEVGDRVFGRGSSTYAEFAVLSAWARIPESLTFEEAAGYPSVVETALRIIRQSGVQSGQTLLVSGASGGVGSAVLQIARDRGIKAIGTAGAASQDYLRGLGALATTYGEGWVERVRQLGQVDAALDLAGSGVIPDLVELTGDPQKVISIADLTAPEHGVRFSGVTGNVPQALVEACDLIARGRLHIPVAKTYQLTEAAAAQADSQAGHTRGRRVIVI
>NZ_CP029192.1|WP_150217448.1|4529746_4530379_+|TetR-family-transcriptional-regulator
MTVPTTPTEPNSPTGSATPPGPSTPPGRRERKKAATRQRIADTAMRLFLERGYDSVGIRDVAAEADVAVTTLFSHFASKEALVFEQDDHFEQRLTQTVTGRTPHEPLIPALRDEVHAMVRHCTADGSAAIYRMIDETRALREYEESMRLRYAESLATAIAADPEFARTTTACRTIARFVVDAYALAREASDPQAAVDEIFRMIEAAWDAA
>NZ_CP029192.1|WP_150217449.1|4530414_4531368_-|SDR-family-NAD(P)-dependent-oxidoreductase
MITEQRKLGTGFGAHSTADDVLAGMDLAGTTALVTGGYSGLGLATTRALVHAGAHVVVPARRPETAENALRDLPRTEVHALDLADLVSVRVFSEGFLATGRSLGILINGAGVMACPETRVGRGWEAHFAINHLGHFALAHRLRPAFAPEGARVVAVASSGHFLSDIRWSDPHFDTGYDRWLAYAQSKTANALFALHLNGLGADHNLRAFAVHPGSILTPLQRHIPRDEWLAQGWMTPDGTPAVGFKSPEQGAATAVWAATSPLLEGRGGAYCQDCDIAEPATSDDMLVGGVKPWAVDPDAAARLWDLSCELTGLSAF
>NZ_CP029192.1|WP_150217450.1|4531438_4531918_+|MerR-family-transcriptional-regulator
MSERPGAVPEESGGNGGGLSIGKVAEATGLSVHALRFFEREELFLREIPRTGGGQRLYEQADVDWLLLCGRLRVSGMPIATIKRFAALVRSGPGNERERLALLQEHERDVRAKIDDLNACLEVIHGKVTTYEQHLRDGTAAGLWSPRPLTTPRRDSSVE
>NZ_CP029192.1|WP_150217451.1|4531981_4532446_+|carboxymuconolactone-decarboxylase-family-protein
MQARMQNPATIFPEAMKAVLSLSGVSRRQGLPQATIELVQLRVSQINGSSVCVEGNVRSAVAAGATDEQCASVAAWRHLSCFTAAERSALALAEAATRLADRPDPVPAEIWDEAARHFTEQELAALVLAIGVANMLNRINIITRRHAGSQPWEC

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_CP029192_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_6

4814136-4814233

Orphan

Consensus_repeat	Method
CCCTGCCCGCCGCTGCGCGGCGAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_6

>merge|NZ_CP029192|6|4814136-4814233|CRISPRCasFinder
CCCTGCCCGCCGCTGCGCGGCGATACGCCCCTCCCACCCGCCCGTGCGCCCCGCACCGATGGGCGCGGGCAGGTCCCTGTCCGCCGCTGCGCGGCGAT

>NZ_CP029192|6|5|4814136-4814233|CRISPRCasFinder
CCCTGCCCGCCGCTGCGCGGCGAT	ACGCCCCTCCCACCCGCCCGTGCGCCCCGCACCGATGGGCGCGGGCAGGT
CCCTGTCCGCCGCTGCGCGGCGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150217654.1\|4804233_4805535_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_055567145.1\|4815617_4816238_+\|DUF47-domain-containing-protein	unknown	unknown	gnl\|CDD\|224310
NZ_CP029192.1\|WP_150221287.1\|4823465_4825742_-\|RNA-degradosome-polyphosphate-kinase	unknown	unknown	gnl\|CDD\|235469
NZ_CP029192.1\|WP_150217662.1\|4814920_4815280_-\|metal-sensing-transcriptional-repressor	unknown	unknown	gnl\|CDD\|376835
NZ_CP029192.1\|WP_150217655.1\|4805534_4806338_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213231
NZ_CP029192.1\|WP_150217657.1\|4807090_4808101_+\|transglycosylase-SLT-domain-containing-protein	unknown	unknown	gnl\|CDD\|381602
NZ_CP029192.1\|WP_150217658.1\|4808349_4809075_+\|phosphatase-PAP2-family-protein	unknown	unknown	gnl\|CDD\|239480
NZ_CP029192.1\|WP_150221285.1\|4812962_4813769_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217653.1\|4803463_4804186_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217666.1\|4820401_4821526_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	unknown	unknown	gnl\|CDD\|270283
NZ_CP029192.1\|WP_150217665.1\|4819264_4820287_-\|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl\|CDD\|273992
NZ_CP029192.1\|WP_150217661.1\|4813863_4814070_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150217664.1\|4818194_4819268_-\|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl\|CDD\|223654
NZ_CP029192.1\|WP_150217659.1\|4809744_4810749_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380149
NZ_CP029192.1\|WP_150221286.1\|4821890_4822328_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239645
NZ_CP029192.1\|WP_150217660.1\|4810954_4812550_-\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223354
NZ_CP029192.1\|WP_150217667.1\|4822363_4823485_-\|CHAD-domain-containing-protein	unknown	unknown	gnl\|CDD\|377493
NZ_CP029192.1\|WP_150217663.1\|4816247_4817246_+\|inorganic-phosphate-transporter	unknown	unknown	gnl\|CDD\|376541
NZ_CP029192.1\|WP_150169539.1\|4817362_4818139_-\|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|184587
NZ_CP029192.1\|WP_150217656.1\|4806370_4806793_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_055567145.1\|4815617_4816238_+\|DUF47-domain-containing-protein	gnl\|CDD\|224310	COG1392, COG1392, Phosphate transport regulator (distant homolog of PhoU) [Inorganic ion transport and metabolism].	1.49623e-30
NZ_CP029192.1\|WP_150169539.1\|4817362_4818139_-\|phosphate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|184587	PRK14241, PRK14241, phosphate transporter ATP-binding protein; Provisional.	0
NZ_CP029192.1\|WP_150217663.1\|4816247_4817246_+\|inorganic-phosphate-transporter	gnl\|CDD\|376541	pfam01384, PHO4, Phosphate transporter family. This family includes PHO-4 from Neurospora crassa which is a is a Na(+)-phosphate symporter. This family also contains the leukaemia virus receptor.	1.39657e-100
NZ_CP029192.1\|WP_150217655.1\|4805534_4806338_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213231	cd03264, ABC_drug_resistance_like, ABC-type multidrug transport system, ATPase component. The biological function of this family is not well characterized, but display ABC domains similar to members of ABCA subfamily. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	4.3649e-94
NZ_CP029192.1\|WP_150217657.1\|4807090_4808101_+\|transglycosylase-SLT-domain-containing-protein	gnl\|CDD\|381602	cd13399, Slt35-like, Slt35-like lytic transglycosylase. Lytic transglycosylase similar to Escherichia coli lytic transglycosylase Slt35 and Pseudomonas aeruginosa Sltb1. Lytic transglycosylase (LT) catalyzes the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc) as do "goose-type" lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. Proteins similar to this this family include the soluble and insoluble membrane-bound LTs in bacteria, the LTs in bacteriophage lambda, as well as the eukaryotic "goose-type" lysozymes (goose egg-white lysozyme; GEWL).	1.52034e-33
NZ_CP029192.1\|WP_150217658.1\|4808349_4809075_+\|phosphatase-PAP2-family-protein	gnl\|CDD\|239480	cd03385, PAP2_BcrC_like, PAP2_like proteins, BcrC_like subfamily. Several members of this family have been annotated as bacitracin transport permeases, as it was suspected that they form the permease component of an ABC transporter system. It was shown, however, that BcrC from Bacillus subtilis posesses undecaprenyl pyrophosphate (UPP) phospatase activity, and it is hypothesized that it competes with bacitracin for UPP, increasing the cell's resistance to bacitracin.	2.88237e-23
NZ_CP029192.1\|WP_150217665.1\|4819264_4820287_-\|phosphate-ABC-transporter-permease-subunit-PstC	gnl\|CDD\|273992	TIGR02138, phosphate_transport_system_permease_protein_PstC, phosphate ABC transporter, permease protein PstC. The typical operon for the high affinity inorganic phosphate ABC transporter encodes an ATP-binding protein, a phosphate-binding protein, and two permease proteins. This family consists of one of the two permease proteins, PstC, which is homologous to PstA (TIGR00974). In the model bacterium Escherichia coli, this transport system is induced when the concentration of extrallular inorganic phosphate is low. A constitutive, lower affinity transporter operates otherwise. [Transport and binding proteins, Anions].	6.38773e-83
NZ_CP029192.1\|WP_150217666.1\|4820401_4821526_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	gnl\|CDD\|270283	cd13565, PBP2_PstS, Substrate binding domain of ABC-type phosphate transporter, a member of the type 2 periplasmic-binding fold superfamily. This subfamily contians phosphate binding domain 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 PBPII 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.	1.96695e-77
NZ_CP029192.1\|WP_150221287.1\|4823465_4825742_-\|RNA-degradosome-polyphosphate-kinase	gnl\|CDD\|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP029192.1\|WP_150217664.1\|4818194_4819268_-\|phosphate-ABC-transporter-permease-PstA	gnl\|CDD\|223654	COG0581, PstA, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	1.50779e-85
NZ_CP029192.1\|WP_150221286.1\|4821890_4822328_-\|NUDIX-domain-containing-protein	gnl\|CDD\|239645	cd03673, Ap6A_hydrolase, Diadenosine hexaphosphate (Ap6A) hydrolase is a member of the Nudix hydrolase superfamily. Ap6A hydrolase specifically hydrolyzes diadenosine polyphosphates, but not ATP or diadenosine triphosphate, and it generates ATP as the product. Ap6A, the most preferred substrate, hydrolyzes to produce two ATP molecules, which is a novel hydrolysis mode for Ap6A. These results indicate that Ap6A hydrolase is a diadenosine polyphosphate hydrolase. It requires the presence of a divalent cation, such as Mn2+, Mg2+, Zn2+, and Co2+, for activity. Members of the Nudix superfamily are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site.	3.70588e-38
NZ_CP029192.1\|WP_150217667.1\|4822363_4823485_-\|CHAD-domain-containing-protein	gnl\|CDD\|377493	pfam05235, CHAD, CHAD domain. The CHAD domain is an alpha-helical domain functionally associated with the pfam01928 domains. It has conserved histidines that may chelate metals.	8.40989e-08
NZ_CP029192.1\|WP_150217660.1\|4810954_4812550_-\|FAD-binding-protein	gnl\|CDD\|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	7.05388e-34
NZ_CP029192.1\|WP_150217662.1\|4814920_4815280_-\|metal-sensing-transcriptional-repressor	gnl\|CDD\|376835	pfam02583, Trns_repr_metal, Metal-sensitive transcriptional repressor. This is a family of metal-sensitive repressors, involved in resistance to metal ions. Members of this family bind copper, nickel or cobalt ions via conserved cysteine and histidine residues. In the absence of metal ions, these proteins bind to promoter regions and repress transcription. When bound to metal ions they are unable to bind DNA, leading to transcriptional derepression.	4.15195e-33
NZ_CP029192.1\|WP_150217659.1\|4809744_4810749_-\|hypothetical-protein	gnl\|CDD\|380149	NF012181, MSCRAMM_SdrD, MSCRAMM family adhesin SdrD. Features of this protein family include a YSIRK-type signal peptide at the N-terminus and a variable-length C-terminal region of Ser-Asp (SD) repeats followed by an LPXTG motif for surface immobilization by sortase.	8.60127e-06

>NZ_CP029192.1|WP_150217661.1|4813863_4814070_+|hypothetical-protein
MNVAPMRGGTAVQDHVALAEIELCGELIIAASAAAERLSFDRIDEVLQVADWRERGVPGEAGGRSPRD
>NZ_CP029192.1|WP_150221285.1|4812962_4813769_+|hypothetical-protein
MGGAGGVVVGAVAFGLMAAASGCSPSGAAADGSGPGDPADVVRRSADSLVRAGSSKASTSMEMASGGTRVTIRGKGVYDFERQVGQFEVVLPQDPAGKDEHRPITELMASGALYMKNRGAGVPSDKWVRIETRSLSDGNLVTGGATDPLAAAELLRGARKVGFVGEERVGGVDVRHYRGVVDLRAAARAASAGQRGALGVAAAKGFSRGSVPFDVYLDDEGRVRKLRQRFAVADANVASTTLFYGFGVPAKVRLPAEKDIFAGKIAGP
>NZ_CP029192.1|WP_150217660.1|4810954_4812550_-|FAD-binding-protein
MERRTFIGTTAATLAAATVAGCSGGTPDGPGTRTGAGATASGGGTRSAGGTPIRTSSAASSSPATLKALARDLDGTLVQPGQAKWAAARQLYNTRYDDLKPTAVAYVAHPDDIRTALAYARAHRTKVAIRNGGHSYAGWSSGNGRLIIDVSKLSKIRASGSSATVGGGAKLIDVYRSLAAKGVTIPAGSCPTVGISGLTLGGGHGVVSRAYGLTCDSLTSATLVTADGKQLTASKSENKDLFWALRGAGNGQFGIVTELTYRTHAAPQGVSAYMTWPWSKAAAVIKAWQEWGPDQPDEIWSSAHLANTPGGTPTVSVACFSLGTYGELQNAVDRLADKIGAPARSVSLKRRTYEESMEVYAGCSSFSADAQCHLPGATPGRSPQGALKRETYAASSDFFDRSLSAAGIRTLLSQIENVTGASGGSIALTALGGAINRVDPTATAFVHRRSRMLAQYIASWRAGTSGSGARAWLNKAHGAMGRYASGAAYQNYTDSTLTNWREAYYGAAAPRLKKLKKQYDPTRFFDFPQAL
>NZ_CP029192.1|WP_150217659.1|4809744_4810749_-|hypothetical-protein
MTPPRSTRIPSGAPRIAAVTATAAAAAVLALAGPAVALDKPTEPGQLTLIDTPEGKALADKDGNPLYTRDADDADTPDCTGECATEWPAAIGYPTKADDVSGQTAQTGDDAPDADKPQVIYETRPLYYYKGDEKGQDPKGQDVKGWSLLGADGKELGAGAGTDGDSDPDTDSDSDSDATDKSASPETSSTSAEKSAPPMASSSPAPSTDASTDASTDASSDTSTEAASQPPANPYTTPTPNPDASATKSPDTRVGALDATPSGAARGGATHAAAEAEHPAAGPLTFASAAVTGAAAGVGVWLLRRRKAHAAAPGTDAVPGPGRGAGPGSGPDHH
>NZ_CP029192.1|WP_150217658.1|4808349_4809075_+|phosphatase-PAP2-family-protein
MAGLDESGSNPDVGLLYDINGLAKDTPSWFDSAAAFVGEYGLLLALVLLVVWCWWGQRKRGTLDDAASSVAAVVWAPLAAGIAVLVNVPIRGFVERPRPFRLHRGVELLVDGKNDYSFVSDHATLAMAIGAGLFVANRKFGIVGLCLAAVEGFLRVFMGVHYPTDVVGGFALGTAVALLLSPLAMALLTPLTKMIGRSGRMGWLVWDRKVAPVAAPLSGTATTTQAAGAASVDPDERDLAA
>NZ_CP029192.1|WP_150217657.1|4807090_4808101_+|transglycosylase-SLT-domain-containing-protein
MRKAWLVASVGIGGALSFIALLVVGTYMAAGSMANGVGGGSVGLAKGAVPATYQPLVQKWGNLCKAINPALLAAQLYQESGFNPRATSPAKAQGIAQFIPGTWASHGLDGDGDGDRDVWDPKDAIPSAASYDCKLAGYVKDAPGNPTKNMLAAYNAGAYAVIKYGGVPPYSETQNYVKTITDLSKSFARPVGRVEPSRQAAGAIYYAQKKLGTLYLWGGNGTPEQGGRFDCSGLTLAAYRSVGVTLPRVANDQYNAGPHPKREELLPGDLVFFSDDLTNSRAIRHVGIYVGGGYMINAPRTGAVIRFDRIDTPDYFGATRVTEDGAKAVPAKPTEV
>NZ_CP029192.1|WP_150217656.1|4806370_4806793_-|hypothetical-protein
MRKRFTGKRKLAVVGVLTAVAISVPAVGAVAAEISGSRLPFALSTAGSKEDGDRWKGKSSGHAKACGDVPVNDTRTFSAYIYQDKSFRPDPKIASTSRSYKQGYGCGAYKGTSTGGKYYTKATWAGIPGSRAYGYVNAQN
>NZ_CP029192.1|WP_150217655.1|4805534_4806338_-|ATP-binding-cassette-domain-containing-protein
MSTPHSAAATGSQPVAAVAGVTVQYGSTTALDDVSLTFPAGVTGLLGPNGAGKSTLLSLLSTARRPKSGDVTLLGETPGRTRVQRLRKQIGVLPQSFGYYPRFTVLEFTEYAAWLRKVPASQRRERAREALRLVQMEKHAGTRMGALSGGMLRRVGIAQAMVNEPSLVLLDEPTVGLDPAQRVGFRKLIKELGDRCAVVMSTHLAEDVAHVCDRVAVLLEGTVRFTGTVAELCALPDGDTGDAGGDIDGSAVEAGYLHLAGTEAVAG
>NZ_CP029192.1|WP_150217654.1|4804233_4805535_-|hypothetical-protein
MRVLLTEMRRGEAKWAAALMGAIGVYYFTAESPDESDWIGWWTQTSLQVQLFSVIVMGSVMSAAAAWSAGRAFRHRTRLWADTAARGSWSQSLLLWLAAWLWALLAYAVLIAVAFSRTAGVSDVSEPAWTPLLLGAGMMGLEIAVGVAVGSALPSRVVAPFAGVFWYSLFVVVAFVPDTPLDKLFPAIDEFWSSEFEPNTTRMLVAVAWCLAFGLALIALPALWRGAALAPRPVALGALTVAALVAGGTLVAFRTPVPDSYWAVRKEQPAQPLCTTSGRTKACLWPDDRHLLPQARAAVRTVDSGLGSLSGLNRSFYADGLDLPSGAGSAELPLMSPAATKDDLTDAMFSAALPQPRSSKCAPHLLKSAGGYPDTFLFEAAVRARIGAPGEYYGEEFGRALERITGAPRAKQDRWIEAAAGDIRACEPVPELP
>NZ_CP029192.1|WP_150217653.1|4803463_4804186_-|hypothetical-protein
MPPANPEPTTPSPTTPSPTSRSEEPARSGLLQDPRLAPVLAFVRCRGLPRAAAVALLVALAATAFAGQRVAVPEFRYLVDFSVPVAEIVPLAHAVILATTLFSPMADLEQTSAQPMSRHRALYLITLLALALGLTALPLLAGATSEVFVSAARNVIGYLGLGMLSARLFGSGLAWLLPLGMFGPTLLLGVGSDNTPEPWAWSLHPSTHTPAMITAVLLWAAGACASATAGPRQSERAEQN
>NZ_CP029192.1|WP_150217662.1|4814920_4815280_-|metal-sensing-transcriptional-repressor
MTTTEAADTADAAVPTPGAPEAPSDQVHGYHKQKDEHLKRLRRIEGQIRGLQRMVEEDVYCIDILTQVSAGTKALQSFALQLLEEHLRHCVADAAVKGGTEIDAKVEEATKAIARMMRT
>NZ_CP029192.1|WP_055567145.1|4815617_4816238_+|DUF47-domain-containing-protein
MRFRLTPRETSFYDMFAASADNIVTGSKLLMELLGADSSARAEIAERMRAAEHAGDDATHAIFHQLNSSFITPFDREDIYNLASSLDDIMDFMEEAVDLVVLYQVEELPKGVEQQIEVLARAAELTAEAMPNLRTMANLTEYWIEVNRLENQADQIHRKLLAQLFNGKYDAIEVLKLKQIVDVLEEAADAFEHVANTVETIAVKES
>NZ_CP029192.1|WP_150217663.1|4816247_4817246_+|inorganic-phosphate-transporter
MDTFALIVTIGVALGFTYTNGFHDSANAIATSVSTRALTPRAALAMAAVMNLAGAFLGSGVAKTVSEGIIETPHGDKGMWILFAALIGAIVWNLITWYFGLPSSSSHALFGGMVGAALAGGIGVIWSGVVDKIVIPMFLSPVVGLVAGYLVMCAIMWMFRKSNPHKAKRGFRIAQTVSAAGMALGHGLQDAQKTMGIVVMALVISDVQSADAPIPIWVKIACALMLSAGTYAGGWRIMRTLGRKIIELDPPQGFAAETTGAGIMFTTAFMFHAPISTTHVITSAIMGVGATKRVNAVRWGVAKNIILGWFITMPAAAIVAALSFWVVDLAFL
>NZ_CP029192.1|WP_150169539.1|4817362_4818139_-|phosphate-ABC-transporter-ATP-binding-protein
MAKRIDVSGLTAFYGSHKAIDDISMTVEPRSVTAFIGPSGCGKSTFLRTLNRMHEVTPGGRVEGKVLLDDEDLYGSGVDPVAVRRTIGMVFQRPNPFPTMSIFDNVAAGLKLNGSYKKSELNDIVEKSLKGANLWNEVKDRLNKPGSGLSGGQQQRLCIARAIAVEPDVLLMDEPCSALDPISTLAIEDLIGELKERFTIVIVTHNMQQAARVSDRTAFFNLAAVGQPGKLIEIDDTERIFSNPSVQATEDYISGRFG
>NZ_CP029192.1|WP_150217664.1|4818194_4819268_-|phosphate-ABC-transporter-permease-PstA
MSTTTPTPTGPLVKRPSTLKAATLPRWTPLVMAAGSAAVAVAIGAAAGLDSRIQWGLIAAVLFIVGSYVLAMGVEGSRQAKDRLATSLVWVMFLLAVVPLASLIYETVQRGIKVFDGYFLTHSMGVVADEETGGGIYHAIIGTLEQVLLASVIAVPIGLLTAVYLVEYGRGKLAKTVTFFVDVMTGIPSIVAGLFVLSFWILILKFDYSGWAGAMALAILMMPVIVRSTEEMLKLVPNELREASLALGVPKWRTILKVVLPTAIGGITTGVMLAVARIAGETAPVLLLVWVNPLINTNPFSGAQGSLPLYIYQQYAAGTEASYDRAWAAALALIGFIMILNMAARAVARWKAPKTGR
>NZ_CP029192.1|WP_150217665.1|4819264_4820287_-|phosphate-ABC-transporter-permease-subunit-PstC
MDIPSNTTAPPPVEDVEPTAPVSKAAARGATRPGDKIFLGLSRGSGIVLLVIMAAIAAFLTYRTTVALSDNTGNFLTTFEWDPAGINTDGKPYFGIAVLVFGTVVSSIIALAIAVPVAIGIALFISHYAPRKLAAPIAYVIDLLAAVPSIVYGLWGALVVAPNLTGLYSWLDDYFGWTGIFAYNGEAPRSLMTVGILLAIMILPIITNVSREVFLQAPKMHEEAALALGATRWEVIRMSVLPFGRSGIISASMLGLGRALGETIAVATVLSPNFLINTSVLDYGGGTFAQNIASKFNEASEYGQDALIASGLVLFIITLLVNGAARLIIARRKEYSGANA
>NZ_CP029192.1|WP_150217666.1|4820401_4821526_-|phosphate-ABC-transporter-substrate-binding-protein-PstS
MKLQRKNRLRALSLGAIAVSGALALTACGSDDTSSGDGGKETNANANIKCDDAKGQLAASGSSAQKNAIDAWRKVYTTNCKDVQLNYNPTGSGAGITAFLQGQTAFAGSDSALKPDEVEKSKKICKGSQAIDLPMVGGPIAIGYNVPGVDSLTLDAKTLGDIFNNKIKTWDDKAIEKLNPDAKLPSTKIQPFHRSDESGTTDNFTKYLKGAAPSAWPYEPGKSWEPKGGQSANGSAGVAGQVKQTAGAISYFELSYAGEGVKTVDLKTEAKEPVKATVDNASKAISEAKVVGKGKDLALELNYKPTAEGAYPITLVTYEVVCEKGNKADTLAATKSFLTYIASEDGQNVLKDNDYAPIPAEIITKVRSTVAGLS
>NZ_CP029192.1|WP_150221286.1|4821890_4822328_-|NUDIX-domain-containing-protein
MPGEETTVLAAGCVLWRPDRAGRDGIELALVHRPKWSDWSHPKGKLKRGETARDAALREVLEETGMACELGAELPTARYRDAQDRPKEVRYWAAEALSGTFAPNSEVSHLRWLAPEEARRLLTRERDAELVNDLLAALAAPRGRA
>NZ_CP029192.1|WP_150217667.1|4822363_4823485_-|CHAD-domain-containing-protein
MAQQHHEMTDTGTGAGPGTAGEALTGYLQDQATEFLRSLRLHRESSTASQGAEESLEAARSLRRAARRIGGTLHTFRPLLDAEWASSLRPELAWLSGTLGQEHAYAGRLDRLLEALHRLSGPSPVPAPAGDPQPASAALAASGAGGRTARQNGWAQPSVPSAADSGTPRGLAVGAAKAAALLERQLTLARTRAHSTALQAFGSSRFHAVADHVAVLASEVPLSGTTEGLVPLADQAEAALAEAVAVLPLGQAGHPYNAGALSHGLAPTDTAPDAQDAPWLKVRSLLRLYRYAQEVLVGHDRTDPRIADASHALNVHREAAAAAAAAAHAARTPRIAPATAYALGVLHADQRHEVEAARFVFQRAWLREEARTR
>NZ_CP029192.1|WP_150221287.1|4823465_4825742_-|RNA-degradosome-polyphosphate-kinase
MVVPARNNGSMSQQNTQGHVQHAQPSVGSIAAHRPATIAATVSDLDPDIDADLDAYDEDAAVGHDGAELPQGRFLDRERSWLAFNERVLELAEDPHTPLLERANFLAIFASNLDEFFMVRVAGLKRRIATGVATRSASGLQPREVLDLIWNRSRELMARHAACYQDDVAPGLADEGIHLVRWHELTEKEQSRLFTLFRQQIFPVLTPLAVDPAHPFPYISGLSLNLAVVVRNPVSGHQHFARVKVPPLLSRFLEASPQRYVPIEDVIAAPAHLQELFPGMEIQEHHMFRLTRNEDLEVEEDDAENLLQALEKELMRRRFGPPVRLEVEESIAPNILSLLVRELKISEAEVYPLPGPLDLTGLFSIAKLDRPELKYPKFVAGTHRDLAEVESASAPDIFAALRERDVLLHHPYDSFSTSVQAFLEQAASDPDVLAIKQTLYRTSGDSPIVDALIDAAESGKQVLVLVEIKARFDEQANIKWARKLEEAGCHVVYGLVGLKTHCKLSLVVRQEGESLVRYSHVGTGNYHPKTARLYEDLGLLTSNAEVGADLSDLFNRLSGYSRRETYRRLLVAPKSLRDGLISRINKEIQHHRAGRPAYVRIKVNSMVDEAVVDALYRASQAGVEVDVWVRGICAVRPGVEGLSENIRVRSVLGRFLEHSRVFAFGNGGEPEVWIGSADMMHRNLDRRIEALVRVQDPAHRAALSRLLETGMSDTTASWHLGADGNWTRHSADPDGQPLRNVQEMLIDARRRRRGTATP

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_CP029192_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_7

5291850-5291912

Unclear

Consensus_repeat	Method
CCCCCGCCGTCCGGCGCTCCGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_7

>merge|NZ_CP029192|7|5291850-5291912|CRISPRCasFinder
CCGCCGCCGCCCGGCGCTCAGGGCACCTCCGCCCCGCAGCCGCCGCCGGCCGGTCCGTCGACG

>NZ_CP029192|7|6|5291850-5291912|CRISPRCasFinder
CCGCCGCCGCCCGGCGCTCAGGG	CACCTCCGCCCCGCAG
CCGCCGCCGGCCGGTCCGTCGACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218010.1\|5295095_5295431_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369438
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341045
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	unknown	unknown	gnl\|CDD\|179535
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	unknown	unknown	gnl\|CDD\|379608
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	unknown	unknown	gnl\|CDD\|379604
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	unknown	unknown	gnl\|CDD\|184641
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl\|CDD\|235457
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373065
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	unknown	unknown	gnl\|CDD\|377315
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	unknown	unknown	gnl\|CDD\|370724
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	unknown	unknown	gnl\|CDD\|235534
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|224316
NZ_CP029192.1\|WP_150218016.1\|5306670_5307090_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl\|CDD\|366019
NZ_CP029192.1\|WP_150218009.1\|5294071_5294974_+\|cellulose-binding-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	unknown	unknown	gnl\|CDD\|271374

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	gnl\|CDD\|369438	pfam07591, PT-HINT, Pretoxin HINT domain. A member of the HINT superfamily of proteases that is usually found N-terminal to the toxin module in polymorphic toxin systems. The domain is predicted to function in releasing the toxin domain by autoproteolysis.	8.20347e-12
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). 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. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) 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.	3.99707e-59
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	gnl\|CDD\|271374	cd11480, SLC5sbd_u4, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	4.56151e-133
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	gnl\|CDD\|379608	pfam14433, SUKH-3, SUKH-3 immunity protein. This family belongs to the SUKH superfamily and functions as immunity proteins in bacterial toxin systems.	1.64687e-64
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	gnl\|CDD\|379604	pfam14414, WHH, A nuclease of the HNH/ENDO VII superfamily with conserved WHH. WHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif WHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. WHH is the shortest version of HNH nuclease families. Like AHH and LHH, the WHH nuclease contains 4 conserved histidines of which the first one is predicted to bind a metal-ion and other three ones are involved in activation of water molecule for hydrolysis.	9.1151e-12
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	gnl\|CDD\|184641	PRK14352, glmU, bifunctional UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase GlmU.	0
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.29148e-35
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	gnl\|CDD\|235457	PRK05426, PRK05426, peptidyl-tRNA hydrolase; Provisional.	1.20743e-94
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	gnl\|CDD\|373065	pfam14431, YwqJ-deaminase, YwqJ-like deaminase. A member of the nucleic acid/nucleotide deaminase superfamily prototyped by Bacillus YwqJ. Members of this family are present in a wide phyletic range of bacteria and a few basidiomycetes. Bacterial versions are predicted to function as toxins in bacterial polymorphic toxin systems.	4.70656e-16
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	gnl\|CDD\|377315	pfam04341, DUF485, Protein of unknown function, DUF485. This family includes several putative integral membrane proteins.	8.85525e-16
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	gnl\|CDD\|370724	pfam09852, DUF2079, Predicted membrane protein (DUF2079). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.1089e-53
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	2.83294e-66
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	gnl\|CDD\|224316	COG1398, OLE1, Fatty-acid desaturase [Lipid metabolism].	3.49193e-70
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	1.88341e-30
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	8.03989e-110
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	gnl\|CDD\|366019	pfam00311, PEPcase, Phosphoenolpyruvate carboxylase.	0
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	gnl\|CDD\|179535	PRK03092, PRK03092, ribose-phosphate diphosphokinase.	0

>NZ_CP029192.1|WP_150218007.1|5289772_5290768_+|cell-wall-assembly-protein-Knr4
MTTGRLGQQSAPPNAAYAGQVVHFPDPVRAARHPRGVRVDERGYPDFSAYARAAAEIAEPPEGFGVDELRLTDYVSANAAMAAADHDLWDTIPAVATPHGWTWHHVPNSRRLELVPVEVKALLRHHGGIATTAVDQNKRGTRPLQETRPAHFGLPKAAVAVTEGQVQSVEEDLGYRLPGAYRSFLKAAGGCAPVGAALDAELGLLVDQPFFTVRDEAAVNDLVYVNKCLRDHLTKDYLGVAFVQGGLLAVKVKGDRIGSVWFCAYDDARDVSEAAGWPPAERVRQLLLPCGDDFDAFLSRLAGNPPELETVANLMVDGGFAHAVSVSSGGE
>NZ_CP029192.1|WP_150221336.1|5288849_5289443_-|hypothetical-protein
MSGQTLATTAGATTGDGTAPATVPTATQAAQAAQAAHTAGDPRVGWSATAAHAPILRQRRDGILPTVAAALSVRGQTTLTCTAGRGEEPPALHPLVQDFLDALTSGQRERFTGRCAEAILISRHLTAADASRSKRASRKPMTNGEARKALKHGKLTTRRIREDGDPLHGHFAQPCRSCTALTAHFGVRVVDPTATEA
>NZ_CP029192.1|WP_150218006.1|5288268_5288799_-|SUKH-3-domain-containing-protein
MHPDHPATAAAPGTGGSTRFPVPVDAALRAAGWRPGHWDIKQAEIWADALRRHTSPAGHRHTVFPAAVEAWAEFGGLHITPQGPGRQIAPATVHLDPMYGLHLARTLGDLGRALGTELCPIGEEPDNQALLAIDTEGRVYSLDHSGDWFLGAHIDQALATLITGAQPTRLSASSGI
>NZ_CP029192.1|WP_150218005.1|5286937_5288251_+|sensor-histidine-kinase
MTTTGDDRTTAMTGPWWWERWRGAALDAGLAVLSAAECGAEGVAFARDAGLPVPVGVGFGVLAGAALLIRRRWPIAVVLISIAITPAQMGVLLTVVGLYTLAASELPRRIIGALAGMSMAGTLVVALVRANQDMAEGSPSIGSEFIPFFAVTAAIGVTAPPVLLGLYVGARRRLVEGMRERADSLERELQLLAERAEERAEWARNEERTRIAREMHDVVAHRVSLMVVHAAALQAVARKDPEKAVRNAALVGDMGRQALTELREMLGVLRTGDGTKAKAEKPAEPPLAAVAFAAAAAASRAVDEDGPCLAELEELVGQSRTAGMAVDLSVEGEARDCSAEVEQTAYRVVQEALTNVHKHAAGAKTHVRLAYRSAEIAMQVENEPPPEADASSDARLPSGGNGLVGMRERVMALGGVFVSGPTDGGGFRVSAVLPAAA
>NZ_CP029192.1|WP_150218004.1|5285003_5286452_-|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU
MSATCPAAVVVLAAGEGTRMKSDRPKVLHDICGRSLIGHVLHAASALSPEQLVTVVGFQSDQVREHLGAIAPQVRTAYQAEQNGTGHAVRIGLEELGGTVDGTVVVVCGDTPLLTGATLQKLAAVHDDDGNAVTVLTAEVPDATGYGRIVRDGADGSVTAIVEHKDATEAQHAIREINSGVFAFDGRLLTEALGKVRTDNSQGEEYLTDVLGILREAGHRVGAAVADDHEEIAGINNRVQLAQARRTLNDRLLTGAMLAGVTVVDPASTWVDATVTFERDAVIQPGTQLHGATHLGKGCEVGPNTRLKDTSVGAGARVDNSVADTAEIGEQALVGPFAYLRPGTRLGVKSKAGTYVEMKNATIGDGSKVPHLSYVGDATIGEHSNIGAASVFVNYDGQAKHHTTVGSHCRTGSDNMFVAPVTVGDGAYTAAGSVITKDVPAGSLAVARGQQRNIEGWVARKRPGSAAAKAAEAASREPAGES
>NZ_CP029192.1|WP_150168841.1|5283915_5284890_-|ribose-phosphate-diphosphokinase
MTGIKTTGEKKLMLFSGRAHPELAEEVAHKLGVGIVPTKAFDFANGEIYVRYQESARGADCFLIQSHTAPINKWIMEQLIMIDALKRASARSITVIVPFYGYARQDKKHRGREPISARLIADLMKTAGADRILTVDLHTDQIQGFFDGPVDHLFALPILADYVGAKVDRSKLTVVSPDAGRVRVADRWCDRLGAPLAIVHKRRDKDVANQVTVHEVVGEVKGRVCVLVDDMIDTGGTICAAADALFAHGAEDVIVTATHGVLSGPAADRLKNSKVSEFVFTDTLPTPSELELDKITVLSIAPTIANAVREVFEDGSVTSLFDEQ
>NZ_CP029192.1|WP_150218003.1|5283145_5283736_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc
MSEVKITAETRSEFGKGAARRLRRADKLPAVVYGHGSEPVHIALPHHDTLMALKTPNVLINLDIEGKSELVIPKAVQRDALRIGILEHVDLLIVKRGEKVTVEVPVHTEGDLAPGNNLLEHVLNTLPVEAEATHIPESVTVSVAGLDAGASVLAKDIPLPSGTTLAVEDDAVVLQVLAAQAEEAPAEDAEGEGDEA
>NZ_CP029192.1|WP_150218002.1|5282433_5283036_-|aminoacyl-tRNA-hydrolase
MHVTTDASAPWLIAGLGNPGPEYAMNRHNVGFMVADLLAQRIGGKFKRAGKAQAQVVEGRIGAPGPANRRVILVKPMSYMNVSGGPVTALRDFYKVPTANIVAVHDELDIDYGTLRLKLGGGDNGHNGLKSMTKAMGPDYHRIRFGIGRPPGRMQVADFVLKDFSSTERKELDYFVDRAADSVEALITEGLERAQSTYNS
>NZ_CP029192.1|WP_150218001.1|5279627_5282372_+|phosphoenolpyruvate-carboxylase
MSSADDQGQQATSTASTELRADIRRLGDLLGETLVRQEGPELLELVEKVRRLTREDGEAAATLLGGTELETAAKLVRAFSTYFHLANVTEQVHRGRELRAKRAAEGGLLARTADRLKDADPEHLRQTVQNLNVRPVFTAHPTEAARRSVLNKLRRVAELLETPVIESDRRRHDIRLAENIDLVWQTDELRVVRPEPADEARNAIYYLDELHAGAVGDVLEDLTAELERVGVELPEGTRPLSFGTWIGGDRDGNPNVTPAVTWDVLILQHEHGINDALDMIDELRGFLSNSIRYTGATEELKSSLQCDLERLPEISPRYKRLNSEEPYRLKATCIRQKLENTKQRLAKGIPHEDGRDYLGTAELLHDLTLIQTSLREHKGALFADGRMNRTIRTLAAFGLQLATMDVREHADAHHHALGQLFDRLGEESWRYADMPREYRQKLLAKELRSRRPLGPSPAPVDAAGEKTLGVFLTVKKALEVFGPEVIESYIISMCQGADDVFAAAVLAREAGLIDLHAGWAKIGIVPLLETTDELRAADVILDEMLADPSYRRLVALRGDVQEVMLGYSDSSKFGGITTSQWEIHRAQRRLRDVAHRYGVRLRLFHGRGGTVGRGGGPSHDAILAQPWGTLEGEIKVTEQGEVISDKYLVPSLARENLELTVAATLQASALHTAPRQSDEALARWDAAMDVVSDAAHSAYRKLVEDPDLPNYFLASTPVDQLADLHLGSRPSRRPGSGVSLDGLRAIPWVFGWTQSRQIVPGWFGVGSGLKALREAGLDTVLDEMHEHWHFFRNFVSNVEMTLAKTDLRIARHYVDTLVPDELKHVFAMIEEEHELTVREVLRITGGDELLDSHPALQQTFAIRDAYLDPISYLQVALLKRQRDAAAAGTDPDPLLGRALLLTVNGVAAGLRNTG
>NZ_CP029192.1|WP_150218000.1|5278284_5279346_-|acyl-CoA-desaturase
MTTTSDAYSEADVIDDAPRADASSATATATPTATAPPSATLGGEQKRSLEQIALLLFITVPFLALVAAVPLAWGWGVSWLDLGLLVFMYYLGCHGITIGFHRYFTHGSFKAKRPLRIALAVAGSMAVEGPLVRWVADHRKHHKFSDAEGDPHSPWRFGETVPALMKGLWWAHIGWMFDEEQTSQEKYAPDLIKDPAIRLISRQFLFWTIVSLAIPPVVGGLVTMSWWGAFTAFFWGSLVRVALLHHVTWSINSICHAVGKRPFKSRDRSGNVWWLAVLSCGESWHNLHHADPTSARHGVMRGQVDSSARIIRWCEQLGWAYDVRWPSQSRIDSRRKPEGAADSRRGAAASDAA
>NZ_CP029192.1|WP_150218009.1|5294071_5294974_+|cellulose-binding-protein
MSSSGASSSPYGFVTVRGRGYRPEQVEAYAAGLSQDRDGAWERAARLTVLAKDMEVEAEHLRDVVSRLAPQTYETLGERARQILALAEAEAAAVRESAAAEAQAVTEDAEAGARELRESARAHAERVGADAEDRAGRRLQADRATADEIRISARQDVKAWRGEALAALREMRQRCEGLLAEQEKEQGERWEAAEREAAEREAASDAHYAERVAAAETRLSEAERAFAEAEESARHGQEDAEARGAEIVAEAVLCEERVTRETERILREHGERWDEVRAHMDHVRSSLATLTGRAPAEETP
>NZ_CP029192.1|WP_150218010.1|5295095_5295431_-|hypothetical-protein
MESDPHLLVEDDRFTALFLLGADDRAEDVENADAELRLPDGTRWSATFMTLREIAAVMDRWKRTGEAAGGAFFQCPDLVVVPTGGVAAMTTAFRAIVDEGGPEGVLPRLED
>NZ_CP029192.1|WP_150218011.1|5295420_5297355_-|hypothetical-protein
MHHRTTTRLVTTVAALSLSFTSAVAAGSPAAAAEKKPASLLEIAERVSHYAHCDDLGLVEKAGCLKEFGRKALIAGAGTALFLYGTQSIMKDHGARFKTLDTELEALGKLKLAELKDPSSTSDPKEQEKILTQAVKTAKAAGPHLANLAKNVAKADEMMGTASDSLYALSILTVVVGDYGYPPSRKVEPIKDKDLPDWGKELRELNAAFDQMNKGFAQMNRGLKTMNEGVDEVNKGLAKANKGISKANKGMKEMNDGIAQANRGMKTANKNVPGIKKGAERLSELPDIDFDFSHVGDSWGSGSSGLDEATQQRRMSLFLDLVPGIGDGKGIVEALTGKDLATGKELSGAERAAGSLAVLRWLKVGAKVGAKALTADDVRKARKGGTAAATCASNSFLPGTRVLMADGSAVPIEQVREGDQVLATEPGTGTTQGRPVTDLIVGDGEKNLVKVDVDVDGDHGDRTASVTATDLHPFWTGDDQWTNAADLAAGTTLRTDAGAPARIAAVTSWTAPDQEVRNLTVAGAHTYYVLVGDTPVLVHNAAPCKIITSAVGKDAQLSKAAQQAGKNQAVQRDLDGLFEQLSRGNMNPGLGSKALAGTDVTYARGRNGGRLFFRNVEGGIEIVGKSDKGNESKVIARLKQLYGK
>NZ_CP029192.1|WP_150221337.1|5297501_5299082_-|cation-acetate-symporter
MSLVAFTVVVTLTLLLCVMTGPDRDDLDEFYTGYGALSPLRNGLAIAGDYISAATVLGTGGVIALLGYDGVVLALSTALSLTLLMFLLAEPLRNAGRFTMGDVVARRMPGRAVRIAACTATIAALLPLMVVQLAGAGDLLAFILGFSSDGLKTGCVVALGALMISYAAIGGMKGTALIQILKIVMLLGSGAVVAALILHRFDWSPGALLAAAQDGSGAGPAYLRSGLQFADSPSPRLDMISSELTVVLGGAALPHVTMRMYTARDAREIRRSMSWAVSSVALFVLVITVVGFGATALLGRATIAEDDPQGNTAYLLGSRAAFGAHTSAAETLIFTTVTTALFLTLLASVAGMILACANSLAHDVFAQGRRTPSPRREMTLARASALAIGVPAIALAILVKDHNLQPLATLSFCLGASALAPALVYSLFWRRYTRTGLLWTLLGGTLGSLILMTGTNLVSGSPGALFPHHDFTWFPFTTTGIASIPLGFLLGWLGTRFSPRAEAEEHRRRYEAVEGWILAGASGRGK
>NZ_CP029192.1|WP_150218012.1|5299099_5299540_-|DUF485-domain-containing-protein
MTDVPYDAYDPAPLPYEQQPHLTYPWQPPPPEAPPAPRLPRRPAPGRHSDLRKLRGAYRIQRRVATLTALGYFTLFLVLSALAPAFMTGTVSGGLTTGLLLGLCQLPVTLLALVLFERTARRRLDPLSELLRRQRESALPRDGEAP
>NZ_CP029192.1|WP_150221338.1|5299651_5301214_-|MFS-transporter
MQGEGSSVGTQDAVRTQDAVRGRGAVVAALMLAMALAAVDSTIVSTAVPQIVGALGGFSIFSWLFSGYLLAATVTLPVYGKLSDTFGRKPVLIAGCVLFLLGSGLCALAWNMESLIAFRVVQGLGGGAVQGTVQTLAADLYPLKERPKIQAKLSTVWATSAVAGPALGGLITSYADWRWIFLINLPIGAVALWLIVRHLHEPAREAVPRGRVDWPGALAVFACGGTLLTALVQGGVAWDWVSVPSFAFFGAGLALIGVVVIVERRAEEPIIPGWVWRRRTIAAVNLALGALGLLMVAPTVFLPTYAQSVLGLAPVAAGFVLSVMTLSWPVSAALSQHVYRRIGFRNTAITGISGAALILFTFPFLPYPGTAWQPALLMLLLGAALGLFQLPLIVGVQSSVGWAERGTATASVLFCRQIGQTLGAALFGAVANGVLAARLDGAGSLDSVARILDDPGSVADPEPLRRAVDAAVDSVYLGAGCAAVAALAVLVFLAPRRFPVLDERQLSSQKDQLSPTQQSD
>NZ_CP029192.1|WP_150218013.1|5301634_5302423_+|ATP-binding-cassette-domain-containing-protein
MTTAITTPRHGGTGGRTAVAARARQVVKAYGSGETRVVALDHIDVDIARGQFTAIMGPSGSGKSTLMHCLAGLDTVSSGQIHLDETEITGLKDKKLTKLRRDRIGFIFQAFNLLPTLNAIENITLPMDIAGRKPDRAWLDQVVETVGLAGRLKHRPTELSGGQQQRVAVARALASRPEIIFGDEPTGNLDSRAGAEVLGFLRRSVTDLGQTIVMVTHDPVAASYADRVLYLADGRIVDEMHHPTADQVLDRMKSFDARGRTS
>NZ_CP029192.1|WP_150218014.1|5302419_5305017_+|FtsX-like-permease-family-protein
MTVLKTSMRNFFAHKGRMALSAVAVILSVAFVCGTLVFSDTMSTTFDKLFAATSADVTVTPKSAEDAGDTPRSGKPESMPASVVQEAKKAKGVKAAEGAVSSQSVTVVNAKNKNMGPTNGGPTIAGNWTHNDLRSMDITSGHAPRGPTEVMIDADTADKHDLKLGDELRTIAATGDLTAKISGIATFKVTNPGAAIVYFDTATSQRQLLGATGRFTHVNLTAAAGVSDTQLKKNVAAVLDGKAAAHDGYDIKTQKEAADDNRESVGSFLDVMKYAMLGFAGIAFLVGIFLIINTFSMLVAQRTREIGLMRAIGSSRKQVNRSVLVEALMLGVFGSVLGVGAGIGLAVGLMKLMSGMGMELSTGDLTVNWTTPVVGLVLGIVVTVLAAYLPARRAGKVSPMAALRDAGTPADGRASALRAVIGLVLTGAGGYALWAASQADKAKDGSLLLGGGVVLSLIGFVVIGPVLASGVVRVISAVLLRMFGPVGRMAERNALRNPRRTGATGAALMIGLALVACLSVVGSSMVASATDELDKSVGADFIVQPTQPGMNITDKAADALGKADHIAHITRYKQINADMTTPSGKTVDGVGLSAADPSYATDLRRETTAGKLSDAYGKNAMSVGDDFAEKHGLKVGDELKIAFEHGRTAKLRLAAITNDDTSVDRGSMYLNITTMEKYVPADRIPQNDMMFASATKGQEEAAYASLKKSLDAYPQYKVMDQTDFKQTLKDQVGQLLNMVYGLLGLAIIVAILGVVNTLALSVVERTREIGLMRAIGLSRRQLRRMIRMESVVIALFGALLGLGLGMGWGATAQKLLALEGLKVLEIPWPTIIAVFIGSAFVGLFAALVPAFRAGRMNVLNAIATE
>NZ_CP029192.1|WP_150218015.1|5305107_5306565_-|DUF2079-domain-containing-protein
MPAAKTDLPAQERADELIPGRDRSVSVPVVDGKRRLWDRAPHLLAAGLFVAYAVVSVCRYRRLESSSWDLGIFEQAVRAYAHLRVPVADLKGPGANILGDHFSPVTALLAPAYRLFPSPVTLLVAQALLIAVSVVPVTRAATRILGRASGLAIGVAYGLSWGIQRAVDFDFHEICFAVPLIAFSLEALLRQRWRASLLWALPLVLVKEDLGATLAALAVVVAIRCRRTDPKALRHALGVAAFGAVATAVTLTLVIPAFNSVGGYDYWDKVGEAGPTAGAFDGFGTKLRTLAWLLIPTSGLLALRSPLLLVALPTLGWRFVSADDHYWGTDWHYSAVLMPVVLLALVDAVDTARRSPKPWLRRYADLLPACVAAAALALTTSLPLAGLTEGATYRKSEQVVAIEKMLDRIPDGATVEANIGPITRLTSRTRVFWTGAADPVVPRYVALDVRSGWTKDPVAYANGLHPGTRYVAEDTAYGYVLLRRE
>NZ_CP029192.1|WP_150218016.1|5306670_5307090_-|hypothetical-protein
MTEPTPPADGGDSLAAALKRAAASGGLAASPVPAHQVAARGARRRRRTYAAGAALAVCLVSGGGALAAVQLGRGGEPVGPAVPPSPTKSASFPESSLADRSPSSGVPSSLTPSTSLPPTATPTWPTPPTATATATPSGG

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_CP029192_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_8

5291997-5292071

Unclear

Consensus_repeat	Method
CCCCCGCCGTCCGGCGCTCCGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_8

>merge|NZ_CP029192|8|5291997-5292071|CRISPRCasFinder
CCTCCGCCGTCCGGCGCTCCGAGCGCTGCGGACGCCTCCGCGTACGGATATCCGCAGCCGCCCGCCGCACCGGCG

>NZ_CP029192|8|7|5291997-5292071|CRISPRCasFinder
CCTCCGCCGTCCGGCGCTCCGAG	CGCTGCGGACGCCTCCGCGTACGGATAT
CCGCAGCCGCCCGCCGCACCGGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218010.1\|5295095_5295431_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369438
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341045
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	unknown	unknown	gnl\|CDD\|179535
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	unknown	unknown	gnl\|CDD\|379608
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	unknown	unknown	gnl\|CDD\|379604
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	unknown	unknown	gnl\|CDD\|184641
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl\|CDD\|235457
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373065
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	unknown	unknown	gnl\|CDD\|377315
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	unknown	unknown	gnl\|CDD\|370724
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	unknown	unknown	gnl\|CDD\|235534
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|224316
NZ_CP029192.1\|WP_150218016.1\|5306670_5307090_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl\|CDD\|366019
NZ_CP029192.1\|WP_150218009.1\|5294071_5294974_+\|cellulose-binding-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	unknown	unknown	gnl\|CDD\|271374

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	gnl\|CDD\|369438	pfam07591, PT-HINT, Pretoxin HINT domain. A member of the HINT superfamily of proteases that is usually found N-terminal to the toxin module in polymorphic toxin systems. The domain is predicted to function in releasing the toxin domain by autoproteolysis.	8.20347e-12
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). 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. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) 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.	3.99707e-59
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	gnl\|CDD\|271374	cd11480, SLC5sbd_u4, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	4.56151e-133
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	gnl\|CDD\|379608	pfam14433, SUKH-3, SUKH-3 immunity protein. This family belongs to the SUKH superfamily and functions as immunity proteins in bacterial toxin systems.	1.64687e-64
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	gnl\|CDD\|379604	pfam14414, WHH, A nuclease of the HNH/ENDO VII superfamily with conserved WHH. WHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif WHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. WHH is the shortest version of HNH nuclease families. Like AHH and LHH, the WHH nuclease contains 4 conserved histidines of which the first one is predicted to bind a metal-ion and other three ones are involved in activation of water molecule for hydrolysis.	9.1151e-12
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	gnl\|CDD\|184641	PRK14352, glmU, bifunctional UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase GlmU.	0
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.29148e-35
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	gnl\|CDD\|235457	PRK05426, PRK05426, peptidyl-tRNA hydrolase; Provisional.	1.20743e-94
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	gnl\|CDD\|373065	pfam14431, YwqJ-deaminase, YwqJ-like deaminase. A member of the nucleic acid/nucleotide deaminase superfamily prototyped by Bacillus YwqJ. Members of this family are present in a wide phyletic range of bacteria and a few basidiomycetes. Bacterial versions are predicted to function as toxins in bacterial polymorphic toxin systems.	4.70656e-16
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	gnl\|CDD\|377315	pfam04341, DUF485, Protein of unknown function, DUF485. This family includes several putative integral membrane proteins.	8.85525e-16
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	gnl\|CDD\|370724	pfam09852, DUF2079, Predicted membrane protein (DUF2079). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.1089e-53
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	2.83294e-66
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	gnl\|CDD\|224316	COG1398, OLE1, Fatty-acid desaturase [Lipid metabolism].	3.49193e-70
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	1.88341e-30
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	8.03989e-110
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	gnl\|CDD\|366019	pfam00311, PEPcase, Phosphoenolpyruvate carboxylase.	0
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	gnl\|CDD\|179535	PRK03092, PRK03092, ribose-phosphate diphosphokinase.	0

>NZ_CP029192.1|WP_150218007.1|5289772_5290768_+|cell-wall-assembly-protein-Knr4
MTTGRLGQQSAPPNAAYAGQVVHFPDPVRAARHPRGVRVDERGYPDFSAYARAAAEIAEPPEGFGVDELRLTDYVSANAAMAAADHDLWDTIPAVATPHGWTWHHVPNSRRLELVPVEVKALLRHHGGIATTAVDQNKRGTRPLQETRPAHFGLPKAAVAVTEGQVQSVEEDLGYRLPGAYRSFLKAAGGCAPVGAALDAELGLLVDQPFFTVRDEAAVNDLVYVNKCLRDHLTKDYLGVAFVQGGLLAVKVKGDRIGSVWFCAYDDARDVSEAAGWPPAERVRQLLLPCGDDFDAFLSRLAGNPPELETVANLMVDGGFAHAVSVSSGGE
>NZ_CP029192.1|WP_150221336.1|5288849_5289443_-|hypothetical-protein
MSGQTLATTAGATTGDGTAPATVPTATQAAQAAQAAHTAGDPRVGWSATAAHAPILRQRRDGILPTVAAALSVRGQTTLTCTAGRGEEPPALHPLVQDFLDALTSGQRERFTGRCAEAILISRHLTAADASRSKRASRKPMTNGEARKALKHGKLTTRRIREDGDPLHGHFAQPCRSCTALTAHFGVRVVDPTATEA
>NZ_CP029192.1|WP_150218006.1|5288268_5288799_-|SUKH-3-domain-containing-protein
MHPDHPATAAAPGTGGSTRFPVPVDAALRAAGWRPGHWDIKQAEIWADALRRHTSPAGHRHTVFPAAVEAWAEFGGLHITPQGPGRQIAPATVHLDPMYGLHLARTLGDLGRALGTELCPIGEEPDNQALLAIDTEGRVYSLDHSGDWFLGAHIDQALATLITGAQPTRLSASSGI
>NZ_CP029192.1|WP_150218005.1|5286937_5288251_+|sensor-histidine-kinase
MTTTGDDRTTAMTGPWWWERWRGAALDAGLAVLSAAECGAEGVAFARDAGLPVPVGVGFGVLAGAALLIRRRWPIAVVLISIAITPAQMGVLLTVVGLYTLAASELPRRIIGALAGMSMAGTLVVALVRANQDMAEGSPSIGSEFIPFFAVTAAIGVTAPPVLLGLYVGARRRLVEGMRERADSLERELQLLAERAEERAEWARNEERTRIAREMHDVVAHRVSLMVVHAAALQAVARKDPEKAVRNAALVGDMGRQALTELREMLGVLRTGDGTKAKAEKPAEPPLAAVAFAAAAAASRAVDEDGPCLAELEELVGQSRTAGMAVDLSVEGEARDCSAEVEQTAYRVVQEALTNVHKHAAGAKTHVRLAYRSAEIAMQVENEPPPEADASSDARLPSGGNGLVGMRERVMALGGVFVSGPTDGGGFRVSAVLPAAA
>NZ_CP029192.1|WP_150218004.1|5285003_5286452_-|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU
MSATCPAAVVVLAAGEGTRMKSDRPKVLHDICGRSLIGHVLHAASALSPEQLVTVVGFQSDQVREHLGAIAPQVRTAYQAEQNGTGHAVRIGLEELGGTVDGTVVVVCGDTPLLTGATLQKLAAVHDDDGNAVTVLTAEVPDATGYGRIVRDGADGSVTAIVEHKDATEAQHAIREINSGVFAFDGRLLTEALGKVRTDNSQGEEYLTDVLGILREAGHRVGAAVADDHEEIAGINNRVQLAQARRTLNDRLLTGAMLAGVTVVDPASTWVDATVTFERDAVIQPGTQLHGATHLGKGCEVGPNTRLKDTSVGAGARVDNSVADTAEIGEQALVGPFAYLRPGTRLGVKSKAGTYVEMKNATIGDGSKVPHLSYVGDATIGEHSNIGAASVFVNYDGQAKHHTTVGSHCRTGSDNMFVAPVTVGDGAYTAAGSVITKDVPAGSLAVARGQQRNIEGWVARKRPGSAAAKAAEAASREPAGES
>NZ_CP029192.1|WP_150168841.1|5283915_5284890_-|ribose-phosphate-diphosphokinase
MTGIKTTGEKKLMLFSGRAHPELAEEVAHKLGVGIVPTKAFDFANGEIYVRYQESARGADCFLIQSHTAPINKWIMEQLIMIDALKRASARSITVIVPFYGYARQDKKHRGREPISARLIADLMKTAGADRILTVDLHTDQIQGFFDGPVDHLFALPILADYVGAKVDRSKLTVVSPDAGRVRVADRWCDRLGAPLAIVHKRRDKDVANQVTVHEVVGEVKGRVCVLVDDMIDTGGTICAAADALFAHGAEDVIVTATHGVLSGPAADRLKNSKVSEFVFTDTLPTPSELELDKITVLSIAPTIANAVREVFEDGSVTSLFDEQ
>NZ_CP029192.1|WP_150218003.1|5283145_5283736_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc
MSEVKITAETRSEFGKGAARRLRRADKLPAVVYGHGSEPVHIALPHHDTLMALKTPNVLINLDIEGKSELVIPKAVQRDALRIGILEHVDLLIVKRGEKVTVEVPVHTEGDLAPGNNLLEHVLNTLPVEAEATHIPESVTVSVAGLDAGASVLAKDIPLPSGTTLAVEDDAVVLQVLAAQAEEAPAEDAEGEGDEA
>NZ_CP029192.1|WP_150218002.1|5282433_5283036_-|aminoacyl-tRNA-hydrolase
MHVTTDASAPWLIAGLGNPGPEYAMNRHNVGFMVADLLAQRIGGKFKRAGKAQAQVVEGRIGAPGPANRRVILVKPMSYMNVSGGPVTALRDFYKVPTANIVAVHDELDIDYGTLRLKLGGGDNGHNGLKSMTKAMGPDYHRIRFGIGRPPGRMQVADFVLKDFSSTERKELDYFVDRAADSVEALITEGLERAQSTYNS
>NZ_CP029192.1|WP_150218001.1|5279627_5282372_+|phosphoenolpyruvate-carboxylase
MSSADDQGQQATSTASTELRADIRRLGDLLGETLVRQEGPELLELVEKVRRLTREDGEAAATLLGGTELETAAKLVRAFSTYFHLANVTEQVHRGRELRAKRAAEGGLLARTADRLKDADPEHLRQTVQNLNVRPVFTAHPTEAARRSVLNKLRRVAELLETPVIESDRRRHDIRLAENIDLVWQTDELRVVRPEPADEARNAIYYLDELHAGAVGDVLEDLTAELERVGVELPEGTRPLSFGTWIGGDRDGNPNVTPAVTWDVLILQHEHGINDALDMIDELRGFLSNSIRYTGATEELKSSLQCDLERLPEISPRYKRLNSEEPYRLKATCIRQKLENTKQRLAKGIPHEDGRDYLGTAELLHDLTLIQTSLREHKGALFADGRMNRTIRTLAAFGLQLATMDVREHADAHHHALGQLFDRLGEESWRYADMPREYRQKLLAKELRSRRPLGPSPAPVDAAGEKTLGVFLTVKKALEVFGPEVIESYIISMCQGADDVFAAAVLAREAGLIDLHAGWAKIGIVPLLETTDELRAADVILDEMLADPSYRRLVALRGDVQEVMLGYSDSSKFGGITTSQWEIHRAQRRLRDVAHRYGVRLRLFHGRGGTVGRGGGPSHDAILAQPWGTLEGEIKVTEQGEVISDKYLVPSLARENLELTVAATLQASALHTAPRQSDEALARWDAAMDVVSDAAHSAYRKLVEDPDLPNYFLASTPVDQLADLHLGSRPSRRPGSGVSLDGLRAIPWVFGWTQSRQIVPGWFGVGSGLKALREAGLDTVLDEMHEHWHFFRNFVSNVEMTLAKTDLRIARHYVDTLVPDELKHVFAMIEEEHELTVREVLRITGGDELLDSHPALQQTFAIRDAYLDPISYLQVALLKRQRDAAAAGTDPDPLLGRALLLTVNGVAAGLRNTG
>NZ_CP029192.1|WP_150218000.1|5278284_5279346_-|acyl-CoA-desaturase
MTTTSDAYSEADVIDDAPRADASSATATATPTATAPPSATLGGEQKRSLEQIALLLFITVPFLALVAAVPLAWGWGVSWLDLGLLVFMYYLGCHGITIGFHRYFTHGSFKAKRPLRIALAVAGSMAVEGPLVRWVADHRKHHKFSDAEGDPHSPWRFGETVPALMKGLWWAHIGWMFDEEQTSQEKYAPDLIKDPAIRLISRQFLFWTIVSLAIPPVVGGLVTMSWWGAFTAFFWGSLVRVALLHHVTWSINSICHAVGKRPFKSRDRSGNVWWLAVLSCGESWHNLHHADPTSARHGVMRGQVDSSARIIRWCEQLGWAYDVRWPSQSRIDSRRKPEGAADSRRGAAASDAA
>NZ_CP029192.1|WP_150218009.1|5294071_5294974_+|cellulose-binding-protein
MSSSGASSSPYGFVTVRGRGYRPEQVEAYAAGLSQDRDGAWERAARLTVLAKDMEVEAEHLRDVVSRLAPQTYETLGERARQILALAEAEAAAVRESAAAEAQAVTEDAEAGARELRESARAHAERVGADAEDRAGRRLQADRATADEIRISARQDVKAWRGEALAALREMRQRCEGLLAEQEKEQGERWEAAEREAAEREAASDAHYAERVAAAETRLSEAERAFAEAEESARHGQEDAEARGAEIVAEAVLCEERVTRETERILREHGERWDEVRAHMDHVRSSLATLTGRAPAEETP
>NZ_CP029192.1|WP_150218010.1|5295095_5295431_-|hypothetical-protein
MESDPHLLVEDDRFTALFLLGADDRAEDVENADAELRLPDGTRWSATFMTLREIAAVMDRWKRTGEAAGGAFFQCPDLVVVPTGGVAAMTTAFRAIVDEGGPEGVLPRLED
>NZ_CP029192.1|WP_150218011.1|5295420_5297355_-|hypothetical-protein
MHHRTTTRLVTTVAALSLSFTSAVAAGSPAAAAEKKPASLLEIAERVSHYAHCDDLGLVEKAGCLKEFGRKALIAGAGTALFLYGTQSIMKDHGARFKTLDTELEALGKLKLAELKDPSSTSDPKEQEKILTQAVKTAKAAGPHLANLAKNVAKADEMMGTASDSLYALSILTVVVGDYGYPPSRKVEPIKDKDLPDWGKELRELNAAFDQMNKGFAQMNRGLKTMNEGVDEVNKGLAKANKGISKANKGMKEMNDGIAQANRGMKTANKNVPGIKKGAERLSELPDIDFDFSHVGDSWGSGSSGLDEATQQRRMSLFLDLVPGIGDGKGIVEALTGKDLATGKELSGAERAAGSLAVLRWLKVGAKVGAKALTADDVRKARKGGTAAATCASNSFLPGTRVLMADGSAVPIEQVREGDQVLATEPGTGTTQGRPVTDLIVGDGEKNLVKVDVDVDGDHGDRTASVTATDLHPFWTGDDQWTNAADLAAGTTLRTDAGAPARIAAVTSWTAPDQEVRNLTVAGAHTYYVLVGDTPVLVHNAAPCKIITSAVGKDAQLSKAAQQAGKNQAVQRDLDGLFEQLSRGNMNPGLGSKALAGTDVTYARGRNGGRLFFRNVEGGIEIVGKSDKGNESKVIARLKQLYGK
>NZ_CP029192.1|WP_150221337.1|5297501_5299082_-|cation-acetate-symporter
MSLVAFTVVVTLTLLLCVMTGPDRDDLDEFYTGYGALSPLRNGLAIAGDYISAATVLGTGGVIALLGYDGVVLALSTALSLTLLMFLLAEPLRNAGRFTMGDVVARRMPGRAVRIAACTATIAALLPLMVVQLAGAGDLLAFILGFSSDGLKTGCVVALGALMISYAAIGGMKGTALIQILKIVMLLGSGAVVAALILHRFDWSPGALLAAAQDGSGAGPAYLRSGLQFADSPSPRLDMISSELTVVLGGAALPHVTMRMYTARDAREIRRSMSWAVSSVALFVLVITVVGFGATALLGRATIAEDDPQGNTAYLLGSRAAFGAHTSAAETLIFTTVTTALFLTLLASVAGMILACANSLAHDVFAQGRRTPSPRREMTLARASALAIGVPAIALAILVKDHNLQPLATLSFCLGASALAPALVYSLFWRRYTRTGLLWTLLGGTLGSLILMTGTNLVSGSPGALFPHHDFTWFPFTTTGIASIPLGFLLGWLGTRFSPRAEAEEHRRRYEAVEGWILAGASGRGK
>NZ_CP029192.1|WP_150218012.1|5299099_5299540_-|DUF485-domain-containing-protein
MTDVPYDAYDPAPLPYEQQPHLTYPWQPPPPEAPPAPRLPRRPAPGRHSDLRKLRGAYRIQRRVATLTALGYFTLFLVLSALAPAFMTGTVSGGLTTGLLLGLCQLPVTLLALVLFERTARRRLDPLSELLRRQRESALPRDGEAP
>NZ_CP029192.1|WP_150221338.1|5299651_5301214_-|MFS-transporter
MQGEGSSVGTQDAVRTQDAVRGRGAVVAALMLAMALAAVDSTIVSTAVPQIVGALGGFSIFSWLFSGYLLAATVTLPVYGKLSDTFGRKPVLIAGCVLFLLGSGLCALAWNMESLIAFRVVQGLGGGAVQGTVQTLAADLYPLKERPKIQAKLSTVWATSAVAGPALGGLITSYADWRWIFLINLPIGAVALWLIVRHLHEPAREAVPRGRVDWPGALAVFACGGTLLTALVQGGVAWDWVSVPSFAFFGAGLALIGVVVIVERRAEEPIIPGWVWRRRTIAAVNLALGALGLLMVAPTVFLPTYAQSVLGLAPVAAGFVLSVMTLSWPVSAALSQHVYRRIGFRNTAITGISGAALILFTFPFLPYPGTAWQPALLMLLLGAALGLFQLPLIVGVQSSVGWAERGTATASVLFCRQIGQTLGAALFGAVANGVLAARLDGAGSLDSVARILDDPGSVADPEPLRRAVDAAVDSVYLGAGCAAVAALAVLVFLAPRRFPVLDERQLSSQKDQLSPTQQSD
>NZ_CP029192.1|WP_150218013.1|5301634_5302423_+|ATP-binding-cassette-domain-containing-protein
MTTAITTPRHGGTGGRTAVAARARQVVKAYGSGETRVVALDHIDVDIARGQFTAIMGPSGSGKSTLMHCLAGLDTVSSGQIHLDETEITGLKDKKLTKLRRDRIGFIFQAFNLLPTLNAIENITLPMDIAGRKPDRAWLDQVVETVGLAGRLKHRPTELSGGQQQRVAVARALASRPEIIFGDEPTGNLDSRAGAEVLGFLRRSVTDLGQTIVMVTHDPVAASYADRVLYLADGRIVDEMHHPTADQVLDRMKSFDARGRTS
>NZ_CP029192.1|WP_150218014.1|5302419_5305017_+|FtsX-like-permease-family-protein
MTVLKTSMRNFFAHKGRMALSAVAVILSVAFVCGTLVFSDTMSTTFDKLFAATSADVTVTPKSAEDAGDTPRSGKPESMPASVVQEAKKAKGVKAAEGAVSSQSVTVVNAKNKNMGPTNGGPTIAGNWTHNDLRSMDITSGHAPRGPTEVMIDADTADKHDLKLGDELRTIAATGDLTAKISGIATFKVTNPGAAIVYFDTATSQRQLLGATGRFTHVNLTAAAGVSDTQLKKNVAAVLDGKAAAHDGYDIKTQKEAADDNRESVGSFLDVMKYAMLGFAGIAFLVGIFLIINTFSMLVAQRTREIGLMRAIGSSRKQVNRSVLVEALMLGVFGSVLGVGAGIGLAVGLMKLMSGMGMELSTGDLTVNWTTPVVGLVLGIVVTVLAAYLPARRAGKVSPMAALRDAGTPADGRASALRAVIGLVLTGAGGYALWAASQADKAKDGSLLLGGGVVLSLIGFVVIGPVLASGVVRVISAVLLRMFGPVGRMAERNALRNPRRTGATGAALMIGLALVACLSVVGSSMVASATDELDKSVGADFIVQPTQPGMNITDKAADALGKADHIAHITRYKQINADMTTPSGKTVDGVGLSAADPSYATDLRRETTAGKLSDAYGKNAMSVGDDFAEKHGLKVGDELKIAFEHGRTAKLRLAAITNDDTSVDRGSMYLNITTMEKYVPADRIPQNDMMFASATKGQEEAAYASLKKSLDAYPQYKVMDQTDFKQTLKDQVGQLLNMVYGLLGLAIIVAILGVVNTLALSVVERTREIGLMRAIGLSRRQLRRMIRMESVVIALFGALLGLGLGMGWGATAQKLLALEGLKVLEIPWPTIIAVFIGSAFVGLFAALVPAFRAGRMNVLNAIATE
>NZ_CP029192.1|WP_150218015.1|5305107_5306565_-|DUF2079-domain-containing-protein
MPAAKTDLPAQERADELIPGRDRSVSVPVVDGKRRLWDRAPHLLAAGLFVAYAVVSVCRYRRLESSSWDLGIFEQAVRAYAHLRVPVADLKGPGANILGDHFSPVTALLAPAYRLFPSPVTLLVAQALLIAVSVVPVTRAATRILGRASGLAIGVAYGLSWGIQRAVDFDFHEICFAVPLIAFSLEALLRQRWRASLLWALPLVLVKEDLGATLAALAVVVAIRCRRTDPKALRHALGVAAFGAVATAVTLTLVIPAFNSVGGYDYWDKVGEAGPTAGAFDGFGTKLRTLAWLLIPTSGLLALRSPLLLVALPTLGWRFVSADDHYWGTDWHYSAVLMPVVLLALVDAVDTARRSPKPWLRRYADLLPACVAAAALALTTSLPLAGLTEGATYRKSEQVVAIEKMLDRIPDGATVEANIGPITRLTSRTRVFWTGAADPVVPRYVALDVRSGWTKDPVAYANGLHPGTRYVAEDTAYGYVLLRRE
>NZ_CP029192.1|WP_150218016.1|5306670_5307090_-|hypothetical-protein
MTEPTPPADGGDSLAAALKRAAASGGLAASPVPAHQVAARGARRRRRTYAAGAALAVCLVSGGGALAAVQLGRGGEPVGPAVPPSPTKSASFPESSLADRSPSSGVPSSLTPSTSLPPTATPTWPTPPTATATATPSGG

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_CP029192_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_10

5292582-5292676

Unclear

Consensus_repeat	Method
CCCCCGCCGTCCGGCGCTCCGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_10

>merge|NZ_CP029192|10|5292582-5292676|CRISPRCasFinder
CCCGGTCCGCCCGGCGCTCCCGGCGCCCCCCAGCCTCCGGGCCCGCCCGGTGCCCCCGGCGCCCCCGGCACGCCCCCGCCCCCCGGCGGTGGCGG

>NZ_CP029192|10|9|5292582-5292676|CRISPRCasFinder
CCCGGTCCGCCCGGCGCTCCCGG	CGCCCCCCAGCCTCCGGGCCCGCCCGGTGCCCCCGGCGCCCCCGGCACG
CCCCCGCCCCCCGGCGGTGGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218010.1\|5295095_5295431_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369438
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341045
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	unknown	unknown	gnl\|CDD\|179535
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	unknown	unknown	gnl\|CDD\|379608
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	unknown	unknown	gnl\|CDD\|379604
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	unknown	unknown	gnl\|CDD\|184641
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl\|CDD\|235457
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373065
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	unknown	unknown	gnl\|CDD\|377315
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	unknown	unknown	gnl\|CDD\|370724
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	unknown	unknown	gnl\|CDD\|235534
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|224316
NZ_CP029192.1\|WP_150218016.1\|5306670_5307090_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl\|CDD\|366019
NZ_CP029192.1\|WP_150218009.1\|5294071_5294974_+\|cellulose-binding-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	unknown	unknown	gnl\|CDD\|271374

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	gnl\|CDD\|369438	pfam07591, PT-HINT, Pretoxin HINT domain. A member of the HINT superfamily of proteases that is usually found N-terminal to the toxin module in polymorphic toxin systems. The domain is predicted to function in releasing the toxin domain by autoproteolysis.	8.20347e-12
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). 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. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) 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.	3.99707e-59
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	gnl\|CDD\|271374	cd11480, SLC5sbd_u4, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	4.56151e-133
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	gnl\|CDD\|379608	pfam14433, SUKH-3, SUKH-3 immunity protein. This family belongs to the SUKH superfamily and functions as immunity proteins in bacterial toxin systems.	1.64687e-64
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	gnl\|CDD\|379604	pfam14414, WHH, A nuclease of the HNH/ENDO VII superfamily with conserved WHH. WHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif WHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. WHH is the shortest version of HNH nuclease families. Like AHH and LHH, the WHH nuclease contains 4 conserved histidines of which the first one is predicted to bind a metal-ion and other three ones are involved in activation of water molecule for hydrolysis.	9.1151e-12
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	gnl\|CDD\|184641	PRK14352, glmU, bifunctional UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase GlmU.	0
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.29148e-35
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	gnl\|CDD\|235457	PRK05426, PRK05426, peptidyl-tRNA hydrolase; Provisional.	1.20743e-94
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	gnl\|CDD\|373065	pfam14431, YwqJ-deaminase, YwqJ-like deaminase. A member of the nucleic acid/nucleotide deaminase superfamily prototyped by Bacillus YwqJ. Members of this family are present in a wide phyletic range of bacteria and a few basidiomycetes. Bacterial versions are predicted to function as toxins in bacterial polymorphic toxin systems.	4.70656e-16
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	gnl\|CDD\|377315	pfam04341, DUF485, Protein of unknown function, DUF485. This family includes several putative integral membrane proteins.	8.85525e-16
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	gnl\|CDD\|370724	pfam09852, DUF2079, Predicted membrane protein (DUF2079). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.1089e-53
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	2.83294e-66
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	gnl\|CDD\|224316	COG1398, OLE1, Fatty-acid desaturase [Lipid metabolism].	3.49193e-70
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	1.88341e-30
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	8.03989e-110
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	gnl\|CDD\|366019	pfam00311, PEPcase, Phosphoenolpyruvate carboxylase.	0
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	gnl\|CDD\|179535	PRK03092, PRK03092, ribose-phosphate diphosphokinase.	0

>NZ_CP029192.1|WP_150218007.1|5289772_5290768_+|cell-wall-assembly-protein-Knr4
MTTGRLGQQSAPPNAAYAGQVVHFPDPVRAARHPRGVRVDERGYPDFSAYARAAAEIAEPPEGFGVDELRLTDYVSANAAMAAADHDLWDTIPAVATPHGWTWHHVPNSRRLELVPVEVKALLRHHGGIATTAVDQNKRGTRPLQETRPAHFGLPKAAVAVTEGQVQSVEEDLGYRLPGAYRSFLKAAGGCAPVGAALDAELGLLVDQPFFTVRDEAAVNDLVYVNKCLRDHLTKDYLGVAFVQGGLLAVKVKGDRIGSVWFCAYDDARDVSEAAGWPPAERVRQLLLPCGDDFDAFLSRLAGNPPELETVANLMVDGGFAHAVSVSSGGE
>NZ_CP029192.1|WP_150221336.1|5288849_5289443_-|hypothetical-protein
MSGQTLATTAGATTGDGTAPATVPTATQAAQAAQAAHTAGDPRVGWSATAAHAPILRQRRDGILPTVAAALSVRGQTTLTCTAGRGEEPPALHPLVQDFLDALTSGQRERFTGRCAEAILISRHLTAADASRSKRASRKPMTNGEARKALKHGKLTTRRIREDGDPLHGHFAQPCRSCTALTAHFGVRVVDPTATEA
>NZ_CP029192.1|WP_150218006.1|5288268_5288799_-|SUKH-3-domain-containing-protein
MHPDHPATAAAPGTGGSTRFPVPVDAALRAAGWRPGHWDIKQAEIWADALRRHTSPAGHRHTVFPAAVEAWAEFGGLHITPQGPGRQIAPATVHLDPMYGLHLARTLGDLGRALGTELCPIGEEPDNQALLAIDTEGRVYSLDHSGDWFLGAHIDQALATLITGAQPTRLSASSGI
>NZ_CP029192.1|WP_150218005.1|5286937_5288251_+|sensor-histidine-kinase
MTTTGDDRTTAMTGPWWWERWRGAALDAGLAVLSAAECGAEGVAFARDAGLPVPVGVGFGVLAGAALLIRRRWPIAVVLISIAITPAQMGVLLTVVGLYTLAASELPRRIIGALAGMSMAGTLVVALVRANQDMAEGSPSIGSEFIPFFAVTAAIGVTAPPVLLGLYVGARRRLVEGMRERADSLERELQLLAERAEERAEWARNEERTRIAREMHDVVAHRVSLMVVHAAALQAVARKDPEKAVRNAALVGDMGRQALTELREMLGVLRTGDGTKAKAEKPAEPPLAAVAFAAAAAASRAVDEDGPCLAELEELVGQSRTAGMAVDLSVEGEARDCSAEVEQTAYRVVQEALTNVHKHAAGAKTHVRLAYRSAEIAMQVENEPPPEADASSDARLPSGGNGLVGMRERVMALGGVFVSGPTDGGGFRVSAVLPAAA
>NZ_CP029192.1|WP_150218004.1|5285003_5286452_-|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU
MSATCPAAVVVLAAGEGTRMKSDRPKVLHDICGRSLIGHVLHAASALSPEQLVTVVGFQSDQVREHLGAIAPQVRTAYQAEQNGTGHAVRIGLEELGGTVDGTVVVVCGDTPLLTGATLQKLAAVHDDDGNAVTVLTAEVPDATGYGRIVRDGADGSVTAIVEHKDATEAQHAIREINSGVFAFDGRLLTEALGKVRTDNSQGEEYLTDVLGILREAGHRVGAAVADDHEEIAGINNRVQLAQARRTLNDRLLTGAMLAGVTVVDPASTWVDATVTFERDAVIQPGTQLHGATHLGKGCEVGPNTRLKDTSVGAGARVDNSVADTAEIGEQALVGPFAYLRPGTRLGVKSKAGTYVEMKNATIGDGSKVPHLSYVGDATIGEHSNIGAASVFVNYDGQAKHHTTVGSHCRTGSDNMFVAPVTVGDGAYTAAGSVITKDVPAGSLAVARGQQRNIEGWVARKRPGSAAAKAAEAASREPAGES
>NZ_CP029192.1|WP_150168841.1|5283915_5284890_-|ribose-phosphate-diphosphokinase
MTGIKTTGEKKLMLFSGRAHPELAEEVAHKLGVGIVPTKAFDFANGEIYVRYQESARGADCFLIQSHTAPINKWIMEQLIMIDALKRASARSITVIVPFYGYARQDKKHRGREPISARLIADLMKTAGADRILTVDLHTDQIQGFFDGPVDHLFALPILADYVGAKVDRSKLTVVSPDAGRVRVADRWCDRLGAPLAIVHKRRDKDVANQVTVHEVVGEVKGRVCVLVDDMIDTGGTICAAADALFAHGAEDVIVTATHGVLSGPAADRLKNSKVSEFVFTDTLPTPSELELDKITVLSIAPTIANAVREVFEDGSVTSLFDEQ
>NZ_CP029192.1|WP_150218003.1|5283145_5283736_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc
MSEVKITAETRSEFGKGAARRLRRADKLPAVVYGHGSEPVHIALPHHDTLMALKTPNVLINLDIEGKSELVIPKAVQRDALRIGILEHVDLLIVKRGEKVTVEVPVHTEGDLAPGNNLLEHVLNTLPVEAEATHIPESVTVSVAGLDAGASVLAKDIPLPSGTTLAVEDDAVVLQVLAAQAEEAPAEDAEGEGDEA
>NZ_CP029192.1|WP_150218002.1|5282433_5283036_-|aminoacyl-tRNA-hydrolase
MHVTTDASAPWLIAGLGNPGPEYAMNRHNVGFMVADLLAQRIGGKFKRAGKAQAQVVEGRIGAPGPANRRVILVKPMSYMNVSGGPVTALRDFYKVPTANIVAVHDELDIDYGTLRLKLGGGDNGHNGLKSMTKAMGPDYHRIRFGIGRPPGRMQVADFVLKDFSSTERKELDYFVDRAADSVEALITEGLERAQSTYNS
>NZ_CP029192.1|WP_150218001.1|5279627_5282372_+|phosphoenolpyruvate-carboxylase
MSSADDQGQQATSTASTELRADIRRLGDLLGETLVRQEGPELLELVEKVRRLTREDGEAAATLLGGTELETAAKLVRAFSTYFHLANVTEQVHRGRELRAKRAAEGGLLARTADRLKDADPEHLRQTVQNLNVRPVFTAHPTEAARRSVLNKLRRVAELLETPVIESDRRRHDIRLAENIDLVWQTDELRVVRPEPADEARNAIYYLDELHAGAVGDVLEDLTAELERVGVELPEGTRPLSFGTWIGGDRDGNPNVTPAVTWDVLILQHEHGINDALDMIDELRGFLSNSIRYTGATEELKSSLQCDLERLPEISPRYKRLNSEEPYRLKATCIRQKLENTKQRLAKGIPHEDGRDYLGTAELLHDLTLIQTSLREHKGALFADGRMNRTIRTLAAFGLQLATMDVREHADAHHHALGQLFDRLGEESWRYADMPREYRQKLLAKELRSRRPLGPSPAPVDAAGEKTLGVFLTVKKALEVFGPEVIESYIISMCQGADDVFAAAVLAREAGLIDLHAGWAKIGIVPLLETTDELRAADVILDEMLADPSYRRLVALRGDVQEVMLGYSDSSKFGGITTSQWEIHRAQRRLRDVAHRYGVRLRLFHGRGGTVGRGGGPSHDAILAQPWGTLEGEIKVTEQGEVISDKYLVPSLARENLELTVAATLQASALHTAPRQSDEALARWDAAMDVVSDAAHSAYRKLVEDPDLPNYFLASTPVDQLADLHLGSRPSRRPGSGVSLDGLRAIPWVFGWTQSRQIVPGWFGVGSGLKALREAGLDTVLDEMHEHWHFFRNFVSNVEMTLAKTDLRIARHYVDTLVPDELKHVFAMIEEEHELTVREVLRITGGDELLDSHPALQQTFAIRDAYLDPISYLQVALLKRQRDAAAAGTDPDPLLGRALLLTVNGVAAGLRNTG
>NZ_CP029192.1|WP_150218000.1|5278284_5279346_-|acyl-CoA-desaturase
MTTTSDAYSEADVIDDAPRADASSATATATPTATAPPSATLGGEQKRSLEQIALLLFITVPFLALVAAVPLAWGWGVSWLDLGLLVFMYYLGCHGITIGFHRYFTHGSFKAKRPLRIALAVAGSMAVEGPLVRWVADHRKHHKFSDAEGDPHSPWRFGETVPALMKGLWWAHIGWMFDEEQTSQEKYAPDLIKDPAIRLISRQFLFWTIVSLAIPPVVGGLVTMSWWGAFTAFFWGSLVRVALLHHVTWSINSICHAVGKRPFKSRDRSGNVWWLAVLSCGESWHNLHHADPTSARHGVMRGQVDSSARIIRWCEQLGWAYDVRWPSQSRIDSRRKPEGAADSRRGAAASDAA
>NZ_CP029192.1|WP_150218009.1|5294071_5294974_+|cellulose-binding-protein
MSSSGASSSPYGFVTVRGRGYRPEQVEAYAAGLSQDRDGAWERAARLTVLAKDMEVEAEHLRDVVSRLAPQTYETLGERARQILALAEAEAAAVRESAAAEAQAVTEDAEAGARELRESARAHAERVGADAEDRAGRRLQADRATADEIRISARQDVKAWRGEALAALREMRQRCEGLLAEQEKEQGERWEAAEREAAEREAASDAHYAERVAAAETRLSEAERAFAEAEESARHGQEDAEARGAEIVAEAVLCEERVTRETERILREHGERWDEVRAHMDHVRSSLATLTGRAPAEETP
>NZ_CP029192.1|WP_150218010.1|5295095_5295431_-|hypothetical-protein
MESDPHLLVEDDRFTALFLLGADDRAEDVENADAELRLPDGTRWSATFMTLREIAAVMDRWKRTGEAAGGAFFQCPDLVVVPTGGVAAMTTAFRAIVDEGGPEGVLPRLED
>NZ_CP029192.1|WP_150218011.1|5295420_5297355_-|hypothetical-protein
MHHRTTTRLVTTVAALSLSFTSAVAAGSPAAAAEKKPASLLEIAERVSHYAHCDDLGLVEKAGCLKEFGRKALIAGAGTALFLYGTQSIMKDHGARFKTLDTELEALGKLKLAELKDPSSTSDPKEQEKILTQAVKTAKAAGPHLANLAKNVAKADEMMGTASDSLYALSILTVVVGDYGYPPSRKVEPIKDKDLPDWGKELRELNAAFDQMNKGFAQMNRGLKTMNEGVDEVNKGLAKANKGISKANKGMKEMNDGIAQANRGMKTANKNVPGIKKGAERLSELPDIDFDFSHVGDSWGSGSSGLDEATQQRRMSLFLDLVPGIGDGKGIVEALTGKDLATGKELSGAERAAGSLAVLRWLKVGAKVGAKALTADDVRKARKGGTAAATCASNSFLPGTRVLMADGSAVPIEQVREGDQVLATEPGTGTTQGRPVTDLIVGDGEKNLVKVDVDVDGDHGDRTASVTATDLHPFWTGDDQWTNAADLAAGTTLRTDAGAPARIAAVTSWTAPDQEVRNLTVAGAHTYYVLVGDTPVLVHNAAPCKIITSAVGKDAQLSKAAQQAGKNQAVQRDLDGLFEQLSRGNMNPGLGSKALAGTDVTYARGRNGGRLFFRNVEGGIEIVGKSDKGNESKVIARLKQLYGK
>NZ_CP029192.1|WP_150221337.1|5297501_5299082_-|cation-acetate-symporter
MSLVAFTVVVTLTLLLCVMTGPDRDDLDEFYTGYGALSPLRNGLAIAGDYISAATVLGTGGVIALLGYDGVVLALSTALSLTLLMFLLAEPLRNAGRFTMGDVVARRMPGRAVRIAACTATIAALLPLMVVQLAGAGDLLAFILGFSSDGLKTGCVVALGALMISYAAIGGMKGTALIQILKIVMLLGSGAVVAALILHRFDWSPGALLAAAQDGSGAGPAYLRSGLQFADSPSPRLDMISSELTVVLGGAALPHVTMRMYTARDAREIRRSMSWAVSSVALFVLVITVVGFGATALLGRATIAEDDPQGNTAYLLGSRAAFGAHTSAAETLIFTTVTTALFLTLLASVAGMILACANSLAHDVFAQGRRTPSPRREMTLARASALAIGVPAIALAILVKDHNLQPLATLSFCLGASALAPALVYSLFWRRYTRTGLLWTLLGGTLGSLILMTGTNLVSGSPGALFPHHDFTWFPFTTTGIASIPLGFLLGWLGTRFSPRAEAEEHRRRYEAVEGWILAGASGRGK
>NZ_CP029192.1|WP_150218012.1|5299099_5299540_-|DUF485-domain-containing-protein
MTDVPYDAYDPAPLPYEQQPHLTYPWQPPPPEAPPAPRLPRRPAPGRHSDLRKLRGAYRIQRRVATLTALGYFTLFLVLSALAPAFMTGTVSGGLTTGLLLGLCQLPVTLLALVLFERTARRRLDPLSELLRRQRESALPRDGEAP
>NZ_CP029192.1|WP_150221338.1|5299651_5301214_-|MFS-transporter
MQGEGSSVGTQDAVRTQDAVRGRGAVVAALMLAMALAAVDSTIVSTAVPQIVGALGGFSIFSWLFSGYLLAATVTLPVYGKLSDTFGRKPVLIAGCVLFLLGSGLCALAWNMESLIAFRVVQGLGGGAVQGTVQTLAADLYPLKERPKIQAKLSTVWATSAVAGPALGGLITSYADWRWIFLINLPIGAVALWLIVRHLHEPAREAVPRGRVDWPGALAVFACGGTLLTALVQGGVAWDWVSVPSFAFFGAGLALIGVVVIVERRAEEPIIPGWVWRRRTIAAVNLALGALGLLMVAPTVFLPTYAQSVLGLAPVAAGFVLSVMTLSWPVSAALSQHVYRRIGFRNTAITGISGAALILFTFPFLPYPGTAWQPALLMLLLGAALGLFQLPLIVGVQSSVGWAERGTATASVLFCRQIGQTLGAALFGAVANGVLAARLDGAGSLDSVARILDDPGSVADPEPLRRAVDAAVDSVYLGAGCAAVAALAVLVFLAPRRFPVLDERQLSSQKDQLSPTQQSD
>NZ_CP029192.1|WP_150218013.1|5301634_5302423_+|ATP-binding-cassette-domain-containing-protein
MTTAITTPRHGGTGGRTAVAARARQVVKAYGSGETRVVALDHIDVDIARGQFTAIMGPSGSGKSTLMHCLAGLDTVSSGQIHLDETEITGLKDKKLTKLRRDRIGFIFQAFNLLPTLNAIENITLPMDIAGRKPDRAWLDQVVETVGLAGRLKHRPTELSGGQQQRVAVARALASRPEIIFGDEPTGNLDSRAGAEVLGFLRRSVTDLGQTIVMVTHDPVAASYADRVLYLADGRIVDEMHHPTADQVLDRMKSFDARGRTS
>NZ_CP029192.1|WP_150218014.1|5302419_5305017_+|FtsX-like-permease-family-protein
MTVLKTSMRNFFAHKGRMALSAVAVILSVAFVCGTLVFSDTMSTTFDKLFAATSADVTVTPKSAEDAGDTPRSGKPESMPASVVQEAKKAKGVKAAEGAVSSQSVTVVNAKNKNMGPTNGGPTIAGNWTHNDLRSMDITSGHAPRGPTEVMIDADTADKHDLKLGDELRTIAATGDLTAKISGIATFKVTNPGAAIVYFDTATSQRQLLGATGRFTHVNLTAAAGVSDTQLKKNVAAVLDGKAAAHDGYDIKTQKEAADDNRESVGSFLDVMKYAMLGFAGIAFLVGIFLIINTFSMLVAQRTREIGLMRAIGSSRKQVNRSVLVEALMLGVFGSVLGVGAGIGLAVGLMKLMSGMGMELSTGDLTVNWTTPVVGLVLGIVVTVLAAYLPARRAGKVSPMAALRDAGTPADGRASALRAVIGLVLTGAGGYALWAASQADKAKDGSLLLGGGVVLSLIGFVVIGPVLASGVVRVISAVLLRMFGPVGRMAERNALRNPRRTGATGAALMIGLALVACLSVVGSSMVASATDELDKSVGADFIVQPTQPGMNITDKAADALGKADHIAHITRYKQINADMTTPSGKTVDGVGLSAADPSYATDLRRETTAGKLSDAYGKNAMSVGDDFAEKHGLKVGDELKIAFEHGRTAKLRLAAITNDDTSVDRGSMYLNITTMEKYVPADRIPQNDMMFASATKGQEEAAYASLKKSLDAYPQYKVMDQTDFKQTLKDQVGQLLNMVYGLLGLAIIVAILGVVNTLALSVVERTREIGLMRAIGLSRRQLRRMIRMESVVIALFGALLGLGLGMGWGATAQKLLALEGLKVLEIPWPTIIAVFIGSAFVGLFAALVPAFRAGRMNVLNAIATE
>NZ_CP029192.1|WP_150218015.1|5305107_5306565_-|DUF2079-domain-containing-protein
MPAAKTDLPAQERADELIPGRDRSVSVPVVDGKRRLWDRAPHLLAAGLFVAYAVVSVCRYRRLESSSWDLGIFEQAVRAYAHLRVPVADLKGPGANILGDHFSPVTALLAPAYRLFPSPVTLLVAQALLIAVSVVPVTRAATRILGRASGLAIGVAYGLSWGIQRAVDFDFHEICFAVPLIAFSLEALLRQRWRASLLWALPLVLVKEDLGATLAALAVVVAIRCRRTDPKALRHALGVAAFGAVATAVTLTLVIPAFNSVGGYDYWDKVGEAGPTAGAFDGFGTKLRTLAWLLIPTSGLLALRSPLLLVALPTLGWRFVSADDHYWGTDWHYSAVLMPVVLLALVDAVDTARRSPKPWLRRYADLLPACVAAAALALTTSLPLAGLTEGATYRKSEQVVAIEKMLDRIPDGATVEANIGPITRLTSRTRVFWTGAADPVVPRYVALDVRSGWTKDPVAYANGLHPGTRYVAEDTAYGYVLLRRE
>NZ_CP029192.1|WP_150218016.1|5306670_5307090_-|hypothetical-protein
MTEPTPPADGGDSLAAALKRAAASGGLAASPVPAHQVAARGARRRRRTYAAGAALAVCLVSGGGALAAVQLGRGGEPVGPAVPPSPTKSASFPESSLADRSPSSGVPSSLTPSTSLPPTATPTWPTPPTATATATPSGG

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_CP029192_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_9

5292357-5292473

Unclear

Consensus_repeat	Method
CCCCCGCCGTCCGGCGCTCCGAG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP029192_9

>merge|NZ_CP029192|9|5292357-5292473|CRISPRCasFinder
CCAGGGGCTCCCGGCGCTCCGGGCACGCCCCCCGGCGCGCCCCAGCCGCCCGGCCCGCCCGGCGCACCCCAGCCGCCCGGCCCGCCCGGCGCACCCCAGCCGCCCGGTCCGCCCGGT

>NZ_CP029192|9|8|5292357-5292473|CRISPRCasFinder
CCAGGGGCTCCCGGCGCTCCGGG	CACGCCCCCCGGCGCG
CCCCAGCCGCCCGGCCCGCCCGG	CGCACCCCAGCCGCCCGGCCCGCCCGGCGCA
CCCCAGCCGCCCGGTCCGCCCGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218010.1\|5295095_5295431_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369438
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341045
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	unknown	unknown	gnl\|CDD\|179535
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	unknown	unknown	gnl\|CDD\|379608
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	unknown	unknown	gnl\|CDD\|379604
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	unknown	unknown	gnl\|CDD\|184641
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl\|CDD\|235457
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373065
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	unknown	unknown	gnl\|CDD\|377315
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	unknown	unknown	gnl\|CDD\|370724
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	unknown	unknown	gnl\|CDD\|235534
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|224316
NZ_CP029192.1\|WP_150218016.1\|5306670_5307090_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl\|CDD\|366019
NZ_CP029192.1\|WP_150218009.1\|5294071_5294974_+\|cellulose-binding-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	unknown	unknown	gnl\|CDD\|271374

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218011.1\|5295420_5297355_-\|hypothetical-protein	gnl\|CDD\|369438	pfam07591, PT-HINT, Pretoxin HINT domain. A member of the HINT superfamily of proteases that is usually found N-terminal to the toxin module in polymorphic toxin systems. The domain is predicted to function in releasing the toxin domain by autoproteolysis.	8.20347e-12
NZ_CP029192.1\|WP_150221338.1\|5299651_5301214_-\|MFS-transporter	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). 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. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) 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.	3.99707e-59
NZ_CP029192.1\|WP_150221337.1\|5297501_5299082_-\|cation-acetate-symporter	gnl\|CDD\|271374	cd11480, SLC5sbd_u4, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	4.56151e-133
NZ_CP029192.1\|WP_150218006.1\|5288268_5288799_-\|SUKH-3-domain-containing-protein	gnl\|CDD\|379608	pfam14433, SUKH-3, SUKH-3 immunity protein. This family belongs to the SUKH superfamily and functions as immunity proteins in bacterial toxin systems.	1.64687e-64
NZ_CP029192.1\|WP_150218007.1\|5289772_5290768_+\|cell-wall-assembly-protein-Knr4	gnl\|CDD\|379604	pfam14414, WHH, A nuclease of the HNH/ENDO VII superfamily with conserved WHH. WHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif WHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. WHH is the shortest version of HNH nuclease families. Like AHH and LHH, the WHH nuclease contains 4 conserved histidines of which the first one is predicted to bind a metal-ion and other three ones are involved in activation of water molecule for hydrolysis.	9.1151e-12
NZ_CP029192.1\|WP_150218004.1\|5285003_5286452_-\|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU	gnl\|CDD\|184641	PRK14352, glmU, bifunctional UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase GlmU.	0
NZ_CP029192.1\|WP_150218005.1\|5286937_5288251_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.29148e-35
NZ_CP029192.1\|WP_150218002.1\|5282433_5283036_-\|aminoacyl-tRNA-hydrolase	gnl\|CDD\|235457	PRK05426, PRK05426, peptidyl-tRNA hydrolase; Provisional.	1.20743e-94
NZ_CP029192.1\|WP_150221336.1\|5288849_5289443_-\|hypothetical-protein	gnl\|CDD\|373065	pfam14431, YwqJ-deaminase, YwqJ-like deaminase. A member of the nucleic acid/nucleotide deaminase superfamily prototyped by Bacillus YwqJ. Members of this family are present in a wide phyletic range of bacteria and a few basidiomycetes. Bacterial versions are predicted to function as toxins in bacterial polymorphic toxin systems.	4.70656e-16
NZ_CP029192.1\|WP_150218012.1\|5299099_5299540_-\|DUF485-domain-containing-protein	gnl\|CDD\|377315	pfam04341, DUF485, Protein of unknown function, DUF485. This family includes several putative integral membrane proteins.	8.85525e-16
NZ_CP029192.1\|WP_150218015.1\|5305107_5306565_-\|DUF2079-domain-containing-protein	gnl\|CDD\|370724	pfam09852, DUF2079, Predicted membrane protein (DUF2079). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.1089e-53
NZ_CP029192.1\|WP_150218003.1\|5283145_5283736_-\|50S-ribosomal-protein-L25/general-stress-protein-Ctc	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	2.83294e-66
NZ_CP029192.1\|WP_150218000.1\|5278284_5279346_-\|acyl-CoA-desaturase	gnl\|CDD\|224316	COG1398, OLE1, Fatty-acid desaturase [Lipid metabolism].	3.49193e-70
NZ_CP029192.1\|WP_150218014.1\|5302419_5305017_+\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	1.88341e-30
NZ_CP029192.1\|WP_150218013.1\|5301634_5302423_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	8.03989e-110
NZ_CP029192.1\|WP_150218001.1\|5279627_5282372_+\|phosphoenolpyruvate-carboxylase	gnl\|CDD\|366019	pfam00311, PEPcase, Phosphoenolpyruvate carboxylase.	0
NZ_CP029192.1\|WP_150168841.1\|5283915_5284890_-\|ribose-phosphate-diphosphokinase	gnl\|CDD\|179535	PRK03092, PRK03092, ribose-phosphate diphosphokinase.	0

>NZ_CP029192.1|WP_150218007.1|5289772_5290768_+|cell-wall-assembly-protein-Knr4
MTTGRLGQQSAPPNAAYAGQVVHFPDPVRAARHPRGVRVDERGYPDFSAYARAAAEIAEPPEGFGVDELRLTDYVSANAAMAAADHDLWDTIPAVATPHGWTWHHVPNSRRLELVPVEVKALLRHHGGIATTAVDQNKRGTRPLQETRPAHFGLPKAAVAVTEGQVQSVEEDLGYRLPGAYRSFLKAAGGCAPVGAALDAELGLLVDQPFFTVRDEAAVNDLVYVNKCLRDHLTKDYLGVAFVQGGLLAVKVKGDRIGSVWFCAYDDARDVSEAAGWPPAERVRQLLLPCGDDFDAFLSRLAGNPPELETVANLMVDGGFAHAVSVSSGGE
>NZ_CP029192.1|WP_150221336.1|5288849_5289443_-|hypothetical-protein
MSGQTLATTAGATTGDGTAPATVPTATQAAQAAQAAHTAGDPRVGWSATAAHAPILRQRRDGILPTVAAALSVRGQTTLTCTAGRGEEPPALHPLVQDFLDALTSGQRERFTGRCAEAILISRHLTAADASRSKRASRKPMTNGEARKALKHGKLTTRRIREDGDPLHGHFAQPCRSCTALTAHFGVRVVDPTATEA
>NZ_CP029192.1|WP_150218006.1|5288268_5288799_-|SUKH-3-domain-containing-protein
MHPDHPATAAAPGTGGSTRFPVPVDAALRAAGWRPGHWDIKQAEIWADALRRHTSPAGHRHTVFPAAVEAWAEFGGLHITPQGPGRQIAPATVHLDPMYGLHLARTLGDLGRALGTELCPIGEEPDNQALLAIDTEGRVYSLDHSGDWFLGAHIDQALATLITGAQPTRLSASSGI
>NZ_CP029192.1|WP_150218005.1|5286937_5288251_+|sensor-histidine-kinase
MTTTGDDRTTAMTGPWWWERWRGAALDAGLAVLSAAECGAEGVAFARDAGLPVPVGVGFGVLAGAALLIRRRWPIAVVLISIAITPAQMGVLLTVVGLYTLAASELPRRIIGALAGMSMAGTLVVALVRANQDMAEGSPSIGSEFIPFFAVTAAIGVTAPPVLLGLYVGARRRLVEGMRERADSLERELQLLAERAEERAEWARNEERTRIAREMHDVVAHRVSLMVVHAAALQAVARKDPEKAVRNAALVGDMGRQALTELREMLGVLRTGDGTKAKAEKPAEPPLAAVAFAAAAAASRAVDEDGPCLAELEELVGQSRTAGMAVDLSVEGEARDCSAEVEQTAYRVVQEALTNVHKHAAGAKTHVRLAYRSAEIAMQVENEPPPEADASSDARLPSGGNGLVGMRERVMALGGVFVSGPTDGGGFRVSAVLPAAA
>NZ_CP029192.1|WP_150218004.1|5285003_5286452_-|bifunctional-UDP-N-acetylglucosamine-diphosphorylase/glucosamine-1-phosphate-N-acetyltransferase-GlmU
MSATCPAAVVVLAAGEGTRMKSDRPKVLHDICGRSLIGHVLHAASALSPEQLVTVVGFQSDQVREHLGAIAPQVRTAYQAEQNGTGHAVRIGLEELGGTVDGTVVVVCGDTPLLTGATLQKLAAVHDDDGNAVTVLTAEVPDATGYGRIVRDGADGSVTAIVEHKDATEAQHAIREINSGVFAFDGRLLTEALGKVRTDNSQGEEYLTDVLGILREAGHRVGAAVADDHEEIAGINNRVQLAQARRTLNDRLLTGAMLAGVTVVDPASTWVDATVTFERDAVIQPGTQLHGATHLGKGCEVGPNTRLKDTSVGAGARVDNSVADTAEIGEQALVGPFAYLRPGTRLGVKSKAGTYVEMKNATIGDGSKVPHLSYVGDATIGEHSNIGAASVFVNYDGQAKHHTTVGSHCRTGSDNMFVAPVTVGDGAYTAAGSVITKDVPAGSLAVARGQQRNIEGWVARKRPGSAAAKAAEAASREPAGES
>NZ_CP029192.1|WP_150168841.1|5283915_5284890_-|ribose-phosphate-diphosphokinase
MTGIKTTGEKKLMLFSGRAHPELAEEVAHKLGVGIVPTKAFDFANGEIYVRYQESARGADCFLIQSHTAPINKWIMEQLIMIDALKRASARSITVIVPFYGYARQDKKHRGREPISARLIADLMKTAGADRILTVDLHTDQIQGFFDGPVDHLFALPILADYVGAKVDRSKLTVVSPDAGRVRVADRWCDRLGAPLAIVHKRRDKDVANQVTVHEVVGEVKGRVCVLVDDMIDTGGTICAAADALFAHGAEDVIVTATHGVLSGPAADRLKNSKVSEFVFTDTLPTPSELELDKITVLSIAPTIANAVREVFEDGSVTSLFDEQ
>NZ_CP029192.1|WP_150218003.1|5283145_5283736_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc
MSEVKITAETRSEFGKGAARRLRRADKLPAVVYGHGSEPVHIALPHHDTLMALKTPNVLINLDIEGKSELVIPKAVQRDALRIGILEHVDLLIVKRGEKVTVEVPVHTEGDLAPGNNLLEHVLNTLPVEAEATHIPESVTVSVAGLDAGASVLAKDIPLPSGTTLAVEDDAVVLQVLAAQAEEAPAEDAEGEGDEA
>NZ_CP029192.1|WP_150218002.1|5282433_5283036_-|aminoacyl-tRNA-hydrolase
MHVTTDASAPWLIAGLGNPGPEYAMNRHNVGFMVADLLAQRIGGKFKRAGKAQAQVVEGRIGAPGPANRRVILVKPMSYMNVSGGPVTALRDFYKVPTANIVAVHDELDIDYGTLRLKLGGGDNGHNGLKSMTKAMGPDYHRIRFGIGRPPGRMQVADFVLKDFSSTERKELDYFVDRAADSVEALITEGLERAQSTYNS
>NZ_CP029192.1|WP_150218001.1|5279627_5282372_+|phosphoenolpyruvate-carboxylase
MSSADDQGQQATSTASTELRADIRRLGDLLGETLVRQEGPELLELVEKVRRLTREDGEAAATLLGGTELETAAKLVRAFSTYFHLANVTEQVHRGRELRAKRAAEGGLLARTADRLKDADPEHLRQTVQNLNVRPVFTAHPTEAARRSVLNKLRRVAELLETPVIESDRRRHDIRLAENIDLVWQTDELRVVRPEPADEARNAIYYLDELHAGAVGDVLEDLTAELERVGVELPEGTRPLSFGTWIGGDRDGNPNVTPAVTWDVLILQHEHGINDALDMIDELRGFLSNSIRYTGATEELKSSLQCDLERLPEISPRYKRLNSEEPYRLKATCIRQKLENTKQRLAKGIPHEDGRDYLGTAELLHDLTLIQTSLREHKGALFADGRMNRTIRTLAAFGLQLATMDVREHADAHHHALGQLFDRLGEESWRYADMPREYRQKLLAKELRSRRPLGPSPAPVDAAGEKTLGVFLTVKKALEVFGPEVIESYIISMCQGADDVFAAAVLAREAGLIDLHAGWAKIGIVPLLETTDELRAADVILDEMLADPSYRRLVALRGDVQEVMLGYSDSSKFGGITTSQWEIHRAQRRLRDVAHRYGVRLRLFHGRGGTVGRGGGPSHDAILAQPWGTLEGEIKVTEQGEVISDKYLVPSLARENLELTVAATLQASALHTAPRQSDEALARWDAAMDVVSDAAHSAYRKLVEDPDLPNYFLASTPVDQLADLHLGSRPSRRPGSGVSLDGLRAIPWVFGWTQSRQIVPGWFGVGSGLKALREAGLDTVLDEMHEHWHFFRNFVSNVEMTLAKTDLRIARHYVDTLVPDELKHVFAMIEEEHELTVREVLRITGGDELLDSHPALQQTFAIRDAYLDPISYLQVALLKRQRDAAAAGTDPDPLLGRALLLTVNGVAAGLRNTG
>NZ_CP029192.1|WP_150218000.1|5278284_5279346_-|acyl-CoA-desaturase
MTTTSDAYSEADVIDDAPRADASSATATATPTATAPPSATLGGEQKRSLEQIALLLFITVPFLALVAAVPLAWGWGVSWLDLGLLVFMYYLGCHGITIGFHRYFTHGSFKAKRPLRIALAVAGSMAVEGPLVRWVADHRKHHKFSDAEGDPHSPWRFGETVPALMKGLWWAHIGWMFDEEQTSQEKYAPDLIKDPAIRLISRQFLFWTIVSLAIPPVVGGLVTMSWWGAFTAFFWGSLVRVALLHHVTWSINSICHAVGKRPFKSRDRSGNVWWLAVLSCGESWHNLHHADPTSARHGVMRGQVDSSARIIRWCEQLGWAYDVRWPSQSRIDSRRKPEGAADSRRGAAASDAA
>NZ_CP029192.1|WP_150218009.1|5294071_5294974_+|cellulose-binding-protein
MSSSGASSSPYGFVTVRGRGYRPEQVEAYAAGLSQDRDGAWERAARLTVLAKDMEVEAEHLRDVVSRLAPQTYETLGERARQILALAEAEAAAVRESAAAEAQAVTEDAEAGARELRESARAHAERVGADAEDRAGRRLQADRATADEIRISARQDVKAWRGEALAALREMRQRCEGLLAEQEKEQGERWEAAEREAAEREAASDAHYAERVAAAETRLSEAERAFAEAEESARHGQEDAEARGAEIVAEAVLCEERVTRETERILREHGERWDEVRAHMDHVRSSLATLTGRAPAEETP
>NZ_CP029192.1|WP_150218010.1|5295095_5295431_-|hypothetical-protein
MESDPHLLVEDDRFTALFLLGADDRAEDVENADAELRLPDGTRWSATFMTLREIAAVMDRWKRTGEAAGGAFFQCPDLVVVPTGGVAAMTTAFRAIVDEGGPEGVLPRLED
>NZ_CP029192.1|WP_150218011.1|5295420_5297355_-|hypothetical-protein
MHHRTTTRLVTTVAALSLSFTSAVAAGSPAAAAEKKPASLLEIAERVSHYAHCDDLGLVEKAGCLKEFGRKALIAGAGTALFLYGTQSIMKDHGARFKTLDTELEALGKLKLAELKDPSSTSDPKEQEKILTQAVKTAKAAGPHLANLAKNVAKADEMMGTASDSLYALSILTVVVGDYGYPPSRKVEPIKDKDLPDWGKELRELNAAFDQMNKGFAQMNRGLKTMNEGVDEVNKGLAKANKGISKANKGMKEMNDGIAQANRGMKTANKNVPGIKKGAERLSELPDIDFDFSHVGDSWGSGSSGLDEATQQRRMSLFLDLVPGIGDGKGIVEALTGKDLATGKELSGAERAAGSLAVLRWLKVGAKVGAKALTADDVRKARKGGTAAATCASNSFLPGTRVLMADGSAVPIEQVREGDQVLATEPGTGTTQGRPVTDLIVGDGEKNLVKVDVDVDGDHGDRTASVTATDLHPFWTGDDQWTNAADLAAGTTLRTDAGAPARIAAVTSWTAPDQEVRNLTVAGAHTYYVLVGDTPVLVHNAAPCKIITSAVGKDAQLSKAAQQAGKNQAVQRDLDGLFEQLSRGNMNPGLGSKALAGTDVTYARGRNGGRLFFRNVEGGIEIVGKSDKGNESKVIARLKQLYGK
>NZ_CP029192.1|WP_150221337.1|5297501_5299082_-|cation-acetate-symporter
MSLVAFTVVVTLTLLLCVMTGPDRDDLDEFYTGYGALSPLRNGLAIAGDYISAATVLGTGGVIALLGYDGVVLALSTALSLTLLMFLLAEPLRNAGRFTMGDVVARRMPGRAVRIAACTATIAALLPLMVVQLAGAGDLLAFILGFSSDGLKTGCVVALGALMISYAAIGGMKGTALIQILKIVMLLGSGAVVAALILHRFDWSPGALLAAAQDGSGAGPAYLRSGLQFADSPSPRLDMISSELTVVLGGAALPHVTMRMYTARDAREIRRSMSWAVSSVALFVLVITVVGFGATALLGRATIAEDDPQGNTAYLLGSRAAFGAHTSAAETLIFTTVTTALFLTLLASVAGMILACANSLAHDVFAQGRRTPSPRREMTLARASALAIGVPAIALAILVKDHNLQPLATLSFCLGASALAPALVYSLFWRRYTRTGLLWTLLGGTLGSLILMTGTNLVSGSPGALFPHHDFTWFPFTTTGIASIPLGFLLGWLGTRFSPRAEAEEHRRRYEAVEGWILAGASGRGK
>NZ_CP029192.1|WP_150218012.1|5299099_5299540_-|DUF485-domain-containing-protein
MTDVPYDAYDPAPLPYEQQPHLTYPWQPPPPEAPPAPRLPRRPAPGRHSDLRKLRGAYRIQRRVATLTALGYFTLFLVLSALAPAFMTGTVSGGLTTGLLLGLCQLPVTLLALVLFERTARRRLDPLSELLRRQRESALPRDGEAP
>NZ_CP029192.1|WP_150221338.1|5299651_5301214_-|MFS-transporter
MQGEGSSVGTQDAVRTQDAVRGRGAVVAALMLAMALAAVDSTIVSTAVPQIVGALGGFSIFSWLFSGYLLAATVTLPVYGKLSDTFGRKPVLIAGCVLFLLGSGLCALAWNMESLIAFRVVQGLGGGAVQGTVQTLAADLYPLKERPKIQAKLSTVWATSAVAGPALGGLITSYADWRWIFLINLPIGAVALWLIVRHLHEPAREAVPRGRVDWPGALAVFACGGTLLTALVQGGVAWDWVSVPSFAFFGAGLALIGVVVIVERRAEEPIIPGWVWRRRTIAAVNLALGALGLLMVAPTVFLPTYAQSVLGLAPVAAGFVLSVMTLSWPVSAALSQHVYRRIGFRNTAITGISGAALILFTFPFLPYPGTAWQPALLMLLLGAALGLFQLPLIVGVQSSVGWAERGTATASVLFCRQIGQTLGAALFGAVANGVLAARLDGAGSLDSVARILDDPGSVADPEPLRRAVDAAVDSVYLGAGCAAVAALAVLVFLAPRRFPVLDERQLSSQKDQLSPTQQSD
>NZ_CP029192.1|WP_150218013.1|5301634_5302423_+|ATP-binding-cassette-domain-containing-protein
MTTAITTPRHGGTGGRTAVAARARQVVKAYGSGETRVVALDHIDVDIARGQFTAIMGPSGSGKSTLMHCLAGLDTVSSGQIHLDETEITGLKDKKLTKLRRDRIGFIFQAFNLLPTLNAIENITLPMDIAGRKPDRAWLDQVVETVGLAGRLKHRPTELSGGQQQRVAVARALASRPEIIFGDEPTGNLDSRAGAEVLGFLRRSVTDLGQTIVMVTHDPVAASYADRVLYLADGRIVDEMHHPTADQVLDRMKSFDARGRTS
>NZ_CP029192.1|WP_150218014.1|5302419_5305017_+|FtsX-like-permease-family-protein
MTVLKTSMRNFFAHKGRMALSAVAVILSVAFVCGTLVFSDTMSTTFDKLFAATSADVTVTPKSAEDAGDTPRSGKPESMPASVVQEAKKAKGVKAAEGAVSSQSVTVVNAKNKNMGPTNGGPTIAGNWTHNDLRSMDITSGHAPRGPTEVMIDADTADKHDLKLGDELRTIAATGDLTAKISGIATFKVTNPGAAIVYFDTATSQRQLLGATGRFTHVNLTAAAGVSDTQLKKNVAAVLDGKAAAHDGYDIKTQKEAADDNRESVGSFLDVMKYAMLGFAGIAFLVGIFLIINTFSMLVAQRTREIGLMRAIGSSRKQVNRSVLVEALMLGVFGSVLGVGAGIGLAVGLMKLMSGMGMELSTGDLTVNWTTPVVGLVLGIVVTVLAAYLPARRAGKVSPMAALRDAGTPADGRASALRAVIGLVLTGAGGYALWAASQADKAKDGSLLLGGGVVLSLIGFVVIGPVLASGVVRVISAVLLRMFGPVGRMAERNALRNPRRTGATGAALMIGLALVACLSVVGSSMVASATDELDKSVGADFIVQPTQPGMNITDKAADALGKADHIAHITRYKQINADMTTPSGKTVDGVGLSAADPSYATDLRRETTAGKLSDAYGKNAMSVGDDFAEKHGLKVGDELKIAFEHGRTAKLRLAAITNDDTSVDRGSMYLNITTMEKYVPADRIPQNDMMFASATKGQEEAAYASLKKSLDAYPQYKVMDQTDFKQTLKDQVGQLLNMVYGLLGLAIIVAILGVVNTLALSVVERTREIGLMRAIGLSRRQLRRMIRMESVVIALFGALLGLGLGMGWGATAQKLLALEGLKVLEIPWPTIIAVFIGSAFVGLFAALVPAFRAGRMNVLNAIATE
>NZ_CP029192.1|WP_150218015.1|5305107_5306565_-|DUF2079-domain-containing-protein
MPAAKTDLPAQERADELIPGRDRSVSVPVVDGKRRLWDRAPHLLAAGLFVAYAVVSVCRYRRLESSSWDLGIFEQAVRAYAHLRVPVADLKGPGANILGDHFSPVTALLAPAYRLFPSPVTLLVAQALLIAVSVVPVTRAATRILGRASGLAIGVAYGLSWGIQRAVDFDFHEICFAVPLIAFSLEALLRQRWRASLLWALPLVLVKEDLGATLAALAVVVAIRCRRTDPKALRHALGVAAFGAVATAVTLTLVIPAFNSVGGYDYWDKVGEAGPTAGAFDGFGTKLRTLAWLLIPTSGLLALRSPLLLVALPTLGWRFVSADDHYWGTDWHYSAVLMPVVLLALVDAVDTARRSPKPWLRRYADLLPACVAAAALALTTSLPLAGLTEGATYRKSEQVVAIEKMLDRIPDGATVEANIGPITRLTSRTRVFWTGAADPVVPRYVALDVRSGWTKDPVAYANGLHPGTRYVAEDTAYGYVLLRRE
>NZ_CP029192.1|WP_150218016.1|5306670_5307090_-|hypothetical-protein
MTEPTPPADGGDSLAAALKRAAASGGLAASPVPAHQVAARGARRRRRTYAAGAALAVCLVSGGGALAAVQLGRGGEPVGPAVPPSPTKSASFPESSLADRSPSSGVPSSLTPSTSLPPTATPTWPTPPTATATATPSGG

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_CP029192_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_11

5321492-5321666

Unclear

Consensus_repeat	Method
CCTAGGGGCGCGGGGAACTGCGCGA	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP029192_11

>merge|NZ_CP029192|11|5321492-5321666|CRISPRCasFinder
CCCAGGGGCGCCGAGAACTGGCTCCGGCGGCGAAGGCTCCCCAGGGGCGCCGAGAACTGGCTCCGGCGGCGAAGGCTCCCTAGGGGCGCGGGGAACTGCGCGAGCAACCACGGTGGATCGGCACCTGGCACACGACCGGGGGACCCACAATCCAGGGGCGCGGGGAACTGCGCGA

>NZ_CP029192|11|10|5321492-5321666|CRISPRCasFinder
CCCAGGGGCGCCGAGAACTGGCTCC	GGCGGCGAAGGCTCCCCAGGGGCGCCGAGAACTGGCTCCGGCGGCGAAGGCTC
CCTAGGGGCGCGGGGAACTGCGCGA	GCAACCACGGTGGATCGGCACCTGGCACACGACCGGGGGACCCACAA
TCCAGGGGCGCGGGGAACTGCGCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218028.1\|5324565_5325282_+\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|369056
NZ_CP029192.1\|WP_150218035.1\|5331037_5332333_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|225139
NZ_CP029192.1\|WP_150218023.1\|5317273_5317903_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370676
NZ_CP029192.1\|WP_150218032.1\|5327568_5328102_+\|DUF501-domain-containing-protein	unknown	unknown	gnl\|CDD\|224424
NZ_CP029192.1\|WP_150218026.1\|5321732_5323016_+\|cytochrome-P450	unknown	unknown	gnl\|CDD\|225035
NZ_CP029192.1\|WP_150218024.1\|5319586_5320255_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372652
NZ_CP029192.1\|WP_150218022.1\|5315055_5317152_+\|N-6-DNA-methylase	unknown	unknown	gnl\|CDD\|280533
NZ_CP029192.1\|WP_150218034.1\|5329437_5330841_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224172
NZ_CP029192.1\|WP_150221341.1\|5317899_5319426_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP029192.1\|WP_150221340.1\|5314048_5314858_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218031.1\|5327031_5327511_+\|septum-formation-initiator-family-protein	unknown	unknown	gnl\|CDD\|368217
NZ_CP029192.1\|WP_150218021.1\|5313283_5314033_+\|N-acetyltransferase	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218029.1\|5325606_5326887_+\|phosphopyruvate-hydratase	unknown	unknown	gnl\|CDD\|234617
NZ_CP029192.1\|WP_150218027.1\|5323154_5324216_+\|transglycosylase-domain-containing-protein	unknown	unknown	gnl\|CDD\|369056
NZ_CP029192.1\|WP_150221339.1\|5312528_5313230_+\|DUF1524-domain-containing-protein	unknown	unknown	gnl\|CDD\|377857
NZ_CP029192.1\|WP_150218019.1\|5311415_5311838_-\|ketosteroid-isomerase	unknown	unknown	gnl\|CDD\|226158
NZ_CP029192.1\|WP_150218020.1\|5311925_5312330_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218025.1\|5320288_5321317_+\|nucleoside-triphosphate-pyrophosphohydrolase	unknown	unknown	gnl\|CDD\|237065
NZ_CP029192.1\|WP_150218036.1\|5332498_5335015_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|226957
NZ_CP029192.1\|WP_150218033.1\|5328098_5329040_+\|Ppx/GppA-family-phosphatase	unknown	unknown	gnl\|CDD\|223326

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218028.1\|5324565_5325282_+\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|369056	pfam06737, Transglycosylas, Transglycosylase-like domain. This family of proteins are very likely to act as transglycosylase enzymes related to pfam00062 and pfam01464. These other families are weakly matched by this family, and include the known active site residues.	1.48802e-36
NZ_CP029192.1\|WP_150218035.1\|5331037_5332333_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|225139	COG2230, Cfa, Cyclopropane fatty acid synthase and related methyltransferases [Cell envelope biogenesis, outer membrane].	1.58029e-115
NZ_CP029192.1\|WP_150218023.1\|5317273_5317903_+\|hypothetical-protein	gnl\|CDD\|370676	pfam09770, PAT1, Topoisomerase II-associated protein PAT1. Members of this family are necessary for accurate chromosome transmission during cell division.	3.32632e-06
NZ_CP029192.1\|WP_150218032.1\|5327568_5328102_+\|DUF501-domain-containing-protein	gnl\|CDD\|224424	COG1507, COG1507, Uncharacterized conserved protein [Function unknown].	2.62274e-60
NZ_CP029192.1\|WP_150218026.1\|5321732_5323016_+\|cytochrome-P450	gnl\|CDD\|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	1.22492e-102
NZ_CP029192.1\|WP_150218024.1\|5319586_5320255_+\|hypothetical-protein	gnl\|CDD\|372652	pfam13624, SurA_N_3, SurA N-terminal domain. This domain is found at the N-terminus of the chaperone SurA. It is a helical domain of unknown function. The C-terminus of the SurA protein folds back and forms part of this domain also but is not included in the current alignment.	5.27343e-10
NZ_CP029192.1\|WP_150218022.1\|5315055_5317152_+\|N-6-DNA-methylase	gnl\|CDD\|280533	pfam02384, N6_Mtase, N-6 DNA Methylase. Restriction-modification (R-M) systems protect a bacterial cell against invasion of foreign DNA by endonucleolytic cleavage of DNA that lacks a site specific modification. The R-M system is a complex containing three polypeptides: M (this family), S (pfam01420), and R. This family consists of N-6 adenine-specific DNA methylase EC:2.1.1.72 from Type I and Type IC restriction systems. These methylases have the same sequence specificity as their corresponding restriction enzymes.	1.49857e-33
NZ_CP029192.1\|WP_150218034.1\|5329437_5330841_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	3.79299e-99
NZ_CP029192.1\|WP_150221341.1\|5317899_5319426_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	3.20235e-102
NZ_CP029192.1\|WP_150218031.1\|5327031_5327511_+\|septum-formation-initiator-family-protein	gnl\|CDD\|368217	pfam04977, DivIC, Septum formation initiator. DivIC from B. subtilis is necessary for both vegetative and sporulation septum formation. These proteins are mainly composed of an amino terminal coiled-coil.	7.53649e-11
NZ_CP029192.1\|WP_150218029.1\|5325606_5326887_+\|phosphopyruvate-hydratase	gnl\|CDD\|234617	PRK00077, eno, enolase; Provisional.	0
NZ_CP029192.1\|WP_150218027.1\|5323154_5324216_+\|transglycosylase-domain-containing-protein	gnl\|CDD\|369056	pfam06737, Transglycosylas, Transglycosylase-like domain. This family of proteins are very likely to act as transglycosylase enzymes related to pfam00062 and pfam01464. These other families are weakly matched by this family, and include the known active site residues.	1.68647e-32
NZ_CP029192.1\|WP_150221339.1\|5312528_5313230_+\|DUF1524-domain-containing-protein	gnl\|CDD\|377857	pfam07510, DUF1524, Protein of unknown function (DUF1524). This family of uncharacterized proteins contain a conserved HXXP motif. A similar motif is seen in protein families in the His-Me finger endonuclease superfamily which suggests this family of proteins may also act as endonucleases.	1.34763e-27
NZ_CP029192.1\|WP_150218019.1\|5311415_5311838_-\|ketosteroid-isomerase	gnl\|CDD\|226158	COG3631, COG3631, Ketosteroid isomerase-related protein [General function prediction only].	2.81205e-10
NZ_CP029192.1\|WP_150218025.1\|5320288_5321317_+\|nucleoside-triphosphate-pyrophosphohydrolase	gnl\|CDD\|237065	PRK12334, PRK12334, nucleoside triphosphate pyrophosphohydrolase; Reviewed.	2.55911e-103
NZ_CP029192.1\|WP_150218036.1\|5332498_5335015_-\|FtsX-like-permease-family-protein	gnl\|CDD\|226957	COG4591, LolE, ABC-type transport system, involved in lipoprotein release, permease component [Cell envelope biogenesis, outer membrane].	9.48605e-23
NZ_CP029192.1\|WP_150218033.1\|5328098_5329040_+\|Ppx/GppA-family-phosphatase	gnl\|CDD\|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	8.06984e-87

>NZ_CP029192.1|WP_150218025.1|5320288_5321317_+|nucleoside-triphosphate-pyrophosphohydrolase
MNQTEPQPPADPSTEPVGRVVLLTTSHRVAPGLLSWPAWQALHAADEVLCADAEHPQLPYLREAGVRVEQAAPAAQELVEACAGGRTVLVVATAEGDRALTDGLARLAGTGRVAMPDLELLPASYDLPGARLLDLVQVMDRIREECPWSSQQTHKGLAKYVIEEAYELVEAIEEGDREELREELGDVLLQVVFHARIAEEATGGDSDDDADDDEEAPFSIDDVAAGIVEKLIHRHPHVFGDDSAQTPEDVRAHWLRTKAEEKRRTSLTEGIPLGQPALALAAKLASRARTASLDVPLPPGEGIGYDLLTLALRAESEGVDPEAALRAAARAYRAAILTAEAR
>NZ_CP029192.1|WP_150218024.1|5319586_5320255_+|hypothetical-protein
MHRRRRTALILSAAAIAAAPLLTACGSKAHPGAAAVVGGDRITVAQLEGRVNEVRDAQRSAIPDDAQYAQAIAKSGGLTRATLHTMVLDKVLHRAATDAGVTVTRRDIQTMRRGMEQQSGGRKALEEGWLQQYNVAPARLDDSLRTEIEAQKLSAKLGADMNSPEGQAVFWKALSAASKKLDIDLNPRYGTWDVDKNKRADAKTPWVRQVTKAQAGPAEQPA
>NZ_CP029192.1|WP_150221341.1|5317899_5319426_+|protein-kinase
MTVRVVAGRYELSTLIGQGGMGQVWTAYDQRLDRRVAVKLLRPDRVAGAEAEELRRRFVRECRVTAQVDHPGLVTVHDAGSEGEDLYLVMQYVDGADLGDHLAEHDPYPWQWAVAIAAQLCAVLSAVHAVPIVHRDLKPRNVMVKQDGTISILDLGIASVMDTDTTRLTHTGSPIGSPAYMAPEQAMGGAVGPYTDLYALGVLMHELLSGDVPFSGSTALGVLHRHLYEPPLPVRRLRPEVPEALEALVLRLLAKDPQHRHGSAQEVYGELAPLLPARGVPSGGPLDPTRPFLRPHAPWPDRAATPAPAPDMPAQPPGTAPQQDVARAVDDVKRLLGEGRITQAVDILGAILPAAAAKHGEHSPVVRTLRKQYAATLMDDGQYRRALPELRRLADERAAESGQADPHSLQFRYEAAQCLEQLGEPAAALAEYRSLLPYYENQYATDDRRQSLEIRRRIGHLLLALGDRTAAHDTLARLLHDAEVLHGPGHPFPAEIMRTLQWLGQVRG
>NZ_CP029192.1|WP_150218023.1|5317273_5317903_+|hypothetical-protein
MHGHGYAPQHPHPPSRGTHVTLRVLFVVLTVLTCGLLAWAAMLRLALVTRKAHNWVLFGIVTALDVLALALVGVDPGEDEFQGPGSAGMVVMLCTMVAAVAYYLYGDIRHFSPYRQQPQPQQPQQYTGYVPQQPQASYGYPQQIAPAPNPAPAPGPPGPVHLQPTQLGHTPPPHPPAPAPARPAPVRIDQVRAELDELSDYLRKQEGGN
>NZ_CP029192.1|WP_150218022.1|5315055_5317152_+|N-6-DNA-methylase
MTPRNDTTEVTAAGIARLAGVGRAAVSNWRRRHGDFPKPVGGTETSPSFALAQVEDWLRAQGKLVEVPLRERLWQQLAGHPAGPVTALLHTGCGLLLLRDRPTDWLAVSAVSDERMAQLLPDVLDETVTMRFGVRRRRAVRIPAAAELLPSVPLLRAAAELASELGAKQTYEFLLGRQTDANPRQYTLTPTGPAELMARIAGSAAPPGTVLDPACGTGALLRAVPPRPDQYLYGQDSSPELAALTALRLALHSDATVRTMAADTLRADAYDDRKAEAVLCHPPFNERNWGHDELAYDARWEYGFPARSESELAWVQHALARLTDGGTAVLLMPPAAASRRSGRRIRADLLRRGALRAVIALPAGTAPPYNLPLHIWVLRKPGPAAKPAPELLLVETAGLLAADGRDRQLWPAVQDAVLDAWEHVERHGTLDERPGTARSVPVLELLDDEVDLAPARHLPPPAAAGGGAELLTVRQGLGEALRRAADLAPPPADLAPADIGDIPRPPLTTVGELARAGALTLHTGTGEGPGGTPVLTDHDVLTGAAPSGTAHESTGSAAGADDVEPVRTAPGDVVVPVFGGGTAARVIDEATAGAALGRGLALLRPDPAALDPWFLAGFLRGTANHRQASSYASTSARLDVRRLQLPRLPLAGQHAYGERFRRLAEFEDAVRRAALLGDRLVRGMHDGLTEGTLPPGAA
>NZ_CP029192.1|WP_150221340.1|5314048_5314858_-|hypothetical-protein
MRRTAAVAAVLVAATVGLTACGSESGKASDAGKASDSTKTKQDKPKEPFAGMSGTEIVNKAVEATKDATSLRLAGDIDDDETGRMKMDLALDTSGKCAGTMSMADEGSFDLIVPGNGTVYMKYDEKFLRSQSKGEPEDQTAAAVEMLADRWSKTKASGPDAKDIAGMCDLDDLLKEFEGGINSNARRGATTELDGIPAIRIDAHDAEEKYTIYVAAEGKPYLLKIIDAEPKKGEAKKAEPEHITFSEYDKPVKTTPPAGKVIDLDKLGA
>NZ_CP029192.1|WP_150218021.1|5313283_5314033_+|N-acetyltransferase
MNLKITTLAERPELTDPLWNMAEDWPEFILHDPVGWSLIGRIVKDLPEYVLVATDEDDGGKVVARAFSVPFALRARGTGELPDGGWDQVLLWAFSDLRHGKRADTVSAIEITVDETARGKGLSARMLDAMRENARAHGFAEVVAPVRPNAKHLEPAARIDEYAYRTREDGLPHDPWLRVHVRAGGVVEKVAHASMTVSGSTAQWREWTGLPFDTEGPVEVPGALVPVHCEPERGYGVYVEPNVWVRHTL
>NZ_CP029192.1|WP_150221339.1|5312528_5313230_+|DUF1524-domain-containing-protein
MLALLAVPALLTGCETGTKDKADGGAAGPDAKAGSALAAVDTLTVKGRAPKTGYERSRFGTAWADTDSNRCPTRDDILKRDLKDVTYAGGDCRVTSGKLAPDPYTGKDVTFRRGRSQVDIDHLVALSDAWQKGAFQWQPAKRIAFANDPLNLLAVDAGPNRGKGDGDTATWLPPNKGYRCTYVAGQVAVKKKYGVWVTGAERAAMKKVLTTCPDEKLPSGTAPTEAPPRFHAR
>NZ_CP029192.1|WP_150218020.1|5311925_5312330_-|hypothetical-protein
MHKRLPRLALPLLTVLVLGTTGCGGSDTNASDTPRTSSPSAHPTPAAPQGRGLKGPAAEFFLKTLRKNYPDLDHIDDDALVAEGDALCTIRGAALGEQFKESTRRLGTTKVQTSRIMGAAHALCRDKDDQLFDR
>NZ_CP029192.1|WP_150218019.1|5311415_5311838_-|ketosteroid-isomerase
MSAADTADRTRAVVQEFLQARLAVDRGRMEELFADDVDWLLAENPAVPWIRPRSTGAECAAQSEELAAHTVPEDARASLDTFLVDGTDAVLFGHLSGTVRATGKSFAGPFALRLTVEDGRITRHHLYENSLSIAAACTTA
>NZ_CP029192.1|WP_150218026.1|5321732_5323016_+|cytochrome-P450
MQDEQPAPPGGTPEPEPELFTWEFASNPYPAYAWLRDNAPVRKTPLPSGVEAWLVTRYADARQALAEPRLSKNPAHHDEPAHAKSKTGIPGERSANLMTHLLNIDPPDHTRLRRLVSKAFTPRRVAEFAPRVQELTDQLIDRFIEEGSADLIHEFAFPLPIYAICDLLGVPREDQDDFRDWAGMMIRHGGGPRGGVARSVKKMRGYLAELIHRKRLEPGDDLISGLIKASDHGEHLTENEAAAMAFILLFAGFETTVNLIGNGMYALLTHPEQRARLQKALAEGDTGLLETGVEELLRFDGPVELATWRFATEPLTIGGQDIAAGDPVLVVLAAADRDPARFEEPDTLDLSRRDNQHLGYGHGIHYCLGAPLARLEGQTALATLLRRLPDLQLAAEPDDLRWRGGLIMRGLRTLPVKFTTAQTTVSD
>NZ_CP029192.1|WP_150218027.1|5323154_5324216_+|transglycosylase-domain-containing-protein
MLSGHGRHRRPRQAPALIVAAGVTGSAIAIPLLGATSANAAETTTWEKLAECESGGEWSANPGNGYYGGLQLSQDTWEAYGGLDYAPSADQASRSQQIAVAEQVLDAKGTAAWPSCAPIAGLTQDGAAADVDPGAPITPKPTDPSDSKGSDKDGEDGKDGKSGKDAKDPSGEDKDKGKGEPSDNASDPEKPSGDASDTPGSGKDSREKNHDESGETGESGEKGETGENESDSGKSGDEDATSPTPENSTDPADDTAGSGGSDDSASGRHRGDRADESESADGRSGRHASRGEKRSGPVADGTYTVRSGDNLSVIADDLGVDGGWHELYTDNKKTVGKDPDLILPGQSLDLGEK
>NZ_CP029192.1|WP_150218028.1|5324565_5325282_+|LysM-peptidoglycan-binding-domain-containing-protein
MLFSSKGKHRRPSKATRVVTLAGVTGAAVAAPLMAAGSASAATTSEWDAVAQCESGGNWSINTGNGYYGGVQFSASTWSAYGGTKYAPTADKASKAQQIEIAEKVLAGQGKGAWPSCGVGLSGASPSTGGGSQEQAPQQKAEPQPQQTQQQAAPQQQAAPKPQPKPQPQTESKKTVETPTGKTVKKGDGEYKVKTGDTLSKIAQAEHVKGGWHKVYKLNGDIIDNADMIYPGQQLHLS
>NZ_CP029192.1|WP_150218029.1|5325606_5326887_+|phosphopyruvate-hydratase
MPSIDVVVAREILDSRGNPTVEVEVGLDDGSTGRAAVPSGASTGAFEAIELRDGDPNRYQGKGVEKAVLAVIEQIGPELVGYDATEQRLIDQAMFDLDATDNKGSLGANAILGVSLAVAHAASEASDLPLFRYLGGPNAHLLPVPMMNILNGGSHADSNVDIQEFMIAPIGAESFSEALRWGTEVYHTLKKVLKDKGLSTGLGDEGGFAPNLDSNRAALDLILEAIKQAGYVPGEQIALALDVAASEFYKDGKYSFEGKDRSAAEMTEYYEELVASYPLVSIEDPLFEDDWAGWNVITEKLGDKVQLVGDDLFVTNPERLARGIEENSANALLVKVNQIGSLTETLDAVEMAQRSGFKCMMSHRSGETEDVTIADLAVATNCGQIKTGAPARSERVAKYNQLLRIEEILDDAAVYAGRSAFPRFKG
>NZ_CP029192.1|WP_150218031.1|5327031_5327511_+|septum-formation-initiator-family-protein
MAKAGTKDRFSTATRLRLLGEQTAERVYRSQTKRQARRSRLTGRAALLALVLCSLVVALAYPMRQYVSQRAEIDDLRRQQAEHRADVEKLRDEKARWQDDAYAEQRVRDRLHYVMPGETGFTVIDPAASKSRRTDQGAATRPWYSNVWDGVDKADRPDD
>NZ_CP029192.1|WP_150218032.1|5327568_5328102_+|DUF501-domain-containing-protein
METPPPTTERTEPTDADVEAFKQQLGRPPRGLRAIAHRCPCGQPDVVETAPRLPDGTPFPTTYYLTCPRAASAIGTLEANGVMKEMSERLKTDEELAKQYRAAHEDYIARRDAIEVLEGFPSAGGMPDRVKCLHVLVGHSLAAGPGVNPLGDEAIAMLPEWWAKGPCVTPCAPEGAE
>NZ_CP029192.1|WP_150218033.1|5328098_5329040_+|Ppx/GppA-family-phosphatase
MTRVAAIDCGTNSIRLLVADADPATGELVDLDRRMTIVRLGQGVDRTGRLAQEALDRTFAACREYAAVIKEHGAERVRFVATSASRDAENRDEFVRGVLDILGVEPEVISGDQEAEFSFTGATKELTGRDDLAKPYLVVDIGGGSTEFVVGTDRVEAARSVDVGCVRMTERHLVRDGVVTDPPAPEQLDAIRADIESALDLAERTVPLKEARTLVGLAGSVTTVAAIALDLDVYDSQAIHHARIPYQRVSAIVDRLTRATHDERAAIPVMHPGRADVIASGALVLLAIMDRVGAREVVVSEHDILDGIGWSIA
>NZ_CP029192.1|WP_150218034.1|5329437_5330841_+|NAD(P)/FAD-dependent-oxidoreductase
MSTTERPRILVVGGGYVGLYAARRILKKMRFGEATVTVVDPRSYMTYQPFLPEAAAGSISPRHVVVPLRRVLPRAEVLTGRVTTIDQDRKVATIAPLVGEAYELPFDYLVIAMGAVSRTFPIPGLAEQGIGMKGIEEAIGLRNHVLEQLDKADSTTDEDVRRKALTFVFVGGGFAGAETIGEVEDMARDAAKYYNNVKREDMRFVLVDVADKILPEVGPKLGQYGKEHLEGRGVEVYLKTGMDSCVDGHVVLNNGLEVDSNTIVWTAGVKPNPALSRFGLPLGPRGHVDTQTTLQVQGTDYIWAAGDNAQVPDMVGRKAGNENAWCPPNAQHALRQAKVLGDNVISGMRGFPQKEYSHANKGAVAGLGLHKGVAMIVMGKMKIKLKGRLAWYMHRAYHGMAMPTFNRKIRVFADWTLGMFLKREVVSLGAMETPREEFYEAAKPAPKPAAAAEPAPAVKAEEKAKAS
>NZ_CP029192.1|WP_150218035.1|5331037_5332333_+|methyltransferase-domain-containing-protein
MQDAAQRLKTLAEQLMGAPLPVRIRAWDGSESGPPNTPALVVRNRRALRHLLWKPGELGLARAWVAGDLDVDGDLYKALDVMAEFIWERGEDSRSLRQSLRDPEFRAAARSLLALSAPFLPPAPPPEEMRRPGRLHLHTKGSDRRAISHHYDVGNDFYALVLGPSMVYSCAYWESPDGTLEDAQRDKLDIVARKLALKPGMRLLDVGCGWGSMAVHAAREYGVSVVGVTLSQEQAAYARKRIAEEGLTDRIEIRVQDYRDVRDGPYDAISSIGMAEHVGSTRYLEYAHDLHALLRPGGRLLNHQIARRPQADESAYSVDEFIDAYVFPDGELAPLGTTVGLLERAGFEVRDVETLREHYALTLRRWVANLEAHWTEGQRLTSPGRARIWRLYMAASALAFERNRIGVNQVLAVKTPEDGASGMPLRARDWR
>NZ_CP029192.1|WP_150218036.1|5332498_5335015_-|FtsX-like-permease-family-protein
MFRTALRNVLAHKARLLMTVLAVMLGVAFVSGTLVFTDTFGNAYKNKSAKSFDHVSVAIQPDGGSSEDGESKEPARLTDGLLKKAAALPGAESAIGSVNGFTALADKDGKLVGGEWGTTGSNYYPGKDGKDPRYAFTKGAAPKSAADIALDSRTAERTGFKVGDTVRYSTDGPVRSAKVSGIFDTDDGSVVAGGSLVVLDNTTALKALNKTEYDEIDVKAAAGTSESALKSSVEKILPKDTDAVTGGQLSDDQDRMIEQQTSSMSQVLLIFAGIALFVGIFIIANTFTMLVAQRTKELALMRAVGASRRQVTRSVLIEAFLVGLVAAVAGFGLGLGVSVGLESLMNSGGASLPDGPLVIAPTTIVVALLIGVVVTMLAAWLPGRRAAKIPPVAAMNSVHATPTTRGLVVRNTIGSLIVAFGTVLLFMDDNYVMAGGAGIILVGVIVLTPLLSRPFIAASAPLLKPFGVTGKLSRLNSVRNPRRTASTASALMIGLTLITGMTVIAVSMGSAINKMAAGSMKADYSVSMANFQELAPEVREKIDKIPDVEASSPLRPAYGEADGSYSVVNGVDPKSFGKLVGLDFTSGSIDDLKAGTALVDTDTAKDKGLKAGDTFPLKFEEDGKTVRLKVAGVYEGNEMLNGLFAPTSVVDPHLSKPVDKQVLVKMKGGASDRAENAIVDALGDNPAITVQDKDDVSNAVAGGINLILNMLYGLLAMAILIAVLGVINTLAMSVFERKHEIGMLRAIGLDRAKVKQMVRLESVVISLFGAVLGIGLGLFMGWAVGGSIAEKVTTYSMEIPVGRIVIFLAIAAVVGVMAAVWPARSAARLNPLMAIKSE

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_CP029192_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_12

5421814-5422130

Orphan

Consensus_repeat	Method
CCAGGGGCGCGGGGAACTGCGCAAGAATGCCCACGACCCGCACCCGA	PILER-CR

3 spacers

The CRISPR arrays of NZ_CP029192_12

>merge|NZ_CP029192|12|5421814-5422130|PILER-CR
CCAGGGGCGCGGGGAACTGCGCAAGAATGCCCACGACCCGCACCCGAACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAAGTACTCCAGGGGCGCGGGGAACTGCGCAAGAAGGCCCACGACCCGCACCCGAACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAACCGGCCCAGGGGCGCGGGGAACTGCGCAAGAATGCCCACGACCCGCACCCGAACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAACCGGCCCAGGGGCGCGGGGAACTGCGCAAGAAAGCCCACGACCCGCACCCGA

>NZ_CP029192|12|1|5421814-5422130|PILER-CR
CCAGGGGCGCGGGGAACTGCGCAAGAATGCCCACGACCCGCACCCGA	ACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAAGTACT
CCAGGGGCGCGGGGAACTGCGCAAGAAGGCCCACGACCCGCACCCGA	ACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAACCGGC
CCAGGGGCGCGGGGAACTGCGCAAGAATGCCCACGACCCGCACCCGA	ACAACATCCCGCGAGCGGAACGTCAAGGCGCCGGGGAACCGGC
CCAGGGGCGCGGGGAACTGCGCAAGAAAGCCCACGACCCGCACCCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218147.1\|5432698_5434315_+\|L-lactate-permease	unknown	unknown	gnl\|CDD\|224535
NZ_CP029192.1\|WP_150218142.1\|5423538_5424495_-\|2-phospho-L-lactate-transferase	unknown	unknown	gnl\|CDD\|237443
NZ_CP029192.1\|WP_150221350.1\|5408235_5409606_-\|LytR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367673
NZ_CP029192.1\|WP_150218126.1\|5409973_5411011_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133016
NZ_CP029192.1\|WP_150218143.1\|5424529_5425045_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380416
NZ_CP029192.1\|WP_016642094.1\|5425688_5425952_+\|WhiB-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376791
NZ_CP029192.1\|WP_150218145.1\|5426183_5429909_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|224137
NZ_CP029192.1\|WP_150218125.1\|5407635_5408184_+\|acyl-CoA-thioesterase	unknown	unknown	gnl\|CDD\|224523
NZ_CP029192.1\|WP_150221352.1\|5431443_5431896_-\|metallopeptidase-family-protein	unknown	unknown	gnl\|CDD\|240574
NZ_CP029192.1\|WP_150218146.1\|5429905_5431396_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218133.1\|5416917_5417697_-\|TIGR03089-family-protein	unknown	unknown	gnl\|CDD\|274426
NZ_CP029192.1\|WP_150218128.1\|5411081_5412833_-\|LytR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367673
NZ_CP029192.1\|WP_150184425.1\|5432158_5432581_+\|DUF3499-family-protein	unknown	unknown	gnl\|CDD\|378788
NZ_CP029192.1\|WP_150218138.1\|5420498_5421503_+\|DNA-3-methyladenine-glycosylase-2-family-protein	unknown	unknown	gnl\|CDD\|223200
NZ_CP029192.1\|WP_150218135.1\|5417816_5419229_+\|peptidoglycan-recognition-protein	unknown	unknown	gnl\|CDD\|128941
NZ_CP029192.1\|WP_150221351.1\|5425224_5425440_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218129.1\|5412934_5414698_-\|LytR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367673
NZ_CP029192.1\|WP_150218140.1\|5422195_5423542_-\|coenzyme-F420-0:L-glutamate-ligase	unknown	unknown	gnl\|CDD\|183957
NZ_CP029192.1\|WP_150218137.1\|5419356_5420439_+\|NTP-transferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|224129
NZ_CP029192.1\|WP_150218131.1\|5414923_5416225_-\|LytR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|367673

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218147.1\|5432698_5434315_+\|L-lactate-permease	gnl\|CDD\|224535	COG1620, LldP, L-lactate permease [Energy production and conversion].	1.48023e-138
NZ_CP029192.1\|WP_150218142.1\|5423538_5424495_-\|2-phospho-L-lactate-transferase	gnl\|CDD\|237443	PRK13606, PRK13606, LPPG:FO 2-phospho-L-lactate transferase; Provisional.	3.13305e-173
NZ_CP029192.1\|WP_150221350.1\|5408235_5409606_-\|LytR-family-transcriptional-regulator	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	1.03336e-54
NZ_CP029192.1\|WP_150218126.1\|5409973_5411011_+\|glycosyltransferase	gnl\|CDD\|133016	cd02525, Succinoglycan_BP_ExoA, ExoA is involved in the biosynthesis of succinoglycan. Succinoglycan Biosynthesis Protein ExoA catalyzes the formation of a beta-1,3 linkage of the second sugar (glucose) of the succinoglycan with the galactose on the lipid carrie. Succinoglycan is an acidic exopolysaccharide that is important for invasion of the nodules. Succinoglycan is a high-molecular-weight polymer composed of repeating octasaccharide units. These units are synthesized on membrane-bound isoprenoid lipid carriers, beginning with galactose followed by seven glucose molecules, and modified by the addition of acetate, succinate, and pyruvate. ExoA is a membrane protein with a transmembrance domain at c-terminus.	1.54597e-92
NZ_CP029192.1\|WP_150218143.1\|5424529_5425045_-\|cupin-domain-containing-protein	gnl\|CDD\|380416	cd10548, cupin_CDO, cysteine dioxygenase, cupin domain. This family contains cysteine dioxygenase (CDO; EC 1.13.11.20), which catalyzes the conversion of cysteine to cysteine sulfinic acid, the first step in the biosynthesis of essential oxidized cysteine metabolites such as sulfate, hypotaurine, and taurine. CDO also plays an important role in the regulation of intracellular cysteine levels in mammals; CDO expression is altered in cancer cells, and abnormal or deficient CDO activity has been linked to Parkinson's disease, Alzheimer's disease, and rheumatoid arthritis. CDO is an iron-dependent thiol dioxygenase that uses molecular oxygen to oxidize the sulfhydryl group of cysteine to generate cysteine sulfinic acid. The CDO active site contains an amino acid-derived cofactor. These enzymes are found in prokaryotes as well as eukaryotes and belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	1.35336e-23
NZ_CP029192.1\|WP_016642094.1\|5425688_5425952_+\|WhiB-family-transcriptional-regulator	gnl\|CDD\|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	4.04301e-28
NZ_CP029192.1\|WP_150218145.1\|5426183_5429909_+\|glycosyltransferase	gnl\|CDD\|224137	COG1216, COG1216, Predicted glycosyltransferases [General function prediction only].	1.2637e-31
NZ_CP029192.1\|WP_150218125.1\|5407635_5408184_+\|acyl-CoA-thioesterase	gnl\|CDD\|224523	COG1607, COG1607, Acyl-CoA hydrolase [Lipid metabolism].	1.44627e-49
NZ_CP029192.1\|WP_150221352.1\|5431443_5431896_-\|metallopeptidase-family-protein	gnl\|CDD\|240574	cd12954, MMP_TTHA0227_like_1, Minimal MMP-like domain found in a group of hypothetical proteins from alphaproteobacteria and actinobacteria. The subfamily includes some uncharacterized bacterial proteins which show high sequence similarity with Thermus thermophilus hypothetical protein TTHA0227. However, they do not contain the conserved HExxH (x could be any amino acid) motif. They may not have any zinc metallo-peptidase activity.	5.8633e-26
NZ_CP029192.1\|WP_150218133.1\|5416917_5417697_-\|TIGR03089-family-protein	gnl\|CDD\|274426	TIGR03089, conserved_hypothetical_protein, TIGR03089 family protein. This protein family is found, so far, only in the Actinobacteria (Streptomyces, Mycobacterium, Corynebacterium, Nocardia, Propionibacterium, etc.) and never more than one to a genome. Members show twilight-level sequence similarity to family of AMP-binding enzymes described by pfam00501.	3.18352e-72
NZ_CP029192.1\|WP_150218128.1\|5411081_5412833_-\|LytR-family-transcriptional-regulator	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	1.54582e-44
NZ_CP029192.1\|WP_150184425.1\|5432158_5432581_+\|DUF3499-family-protein	gnl\|CDD\|378788	pfam12005, DUF3499, Protein of unknown function (DUF3499). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 125 to 163 amino acids in length.	4.41406e-58
NZ_CP029192.1\|WP_150218138.1\|5420498_5421503_+\|DNA-3-methyladenine-glycosylase-2-family-protein	gnl\|CDD\|223200	COG0122, AlkA, 3-methyladenine DNA glycosylase/8-oxoguanine DNA glycosylase [DNA replication, recombination, and repair].	2.5681e-25
NZ_CP029192.1\|WP_150218135.1\|5417816_5419229_+\|peptidoglycan-recognition-protein	gnl\|CDD\|128941	smart00701, PGRP, Animal peptidoglycan recognition proteins homologous to Bacteriophage T3 lysozyme. The bacteriophage molecule, but not its moth homologue, has been shown to have N-acetylmuramoyl-L-alanine amidase activity. One member of this family, Tag7, is a cytokine.	2.99896e-47
NZ_CP029192.1\|WP_150218129.1\|5412934_5414698_-\|LytR-family-transcriptional-regulator	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	7.39289e-54
NZ_CP029192.1\|WP_150218140.1\|5422195_5423542_-\|coenzyme-F420-0:L-glutamate-ligase	gnl\|CDD\|183957	PRK13294, PRK13294, F420-0--gamma-glutamyl ligase; Provisional.	0
NZ_CP029192.1\|WP_150218137.1\|5419356_5420439_+\|NTP-transferase-domain-containing-protein	gnl\|CDD\|224129	COG1208, GCD1, Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis/translation initiation factor 2B, gamma/epsilon subunits (eIF-2Bgamma/eIF-2Bepsilon) [Cell envelope biogenesis, outer membrane / Translation, ribosomal structure and biogenesis].	5.61071e-106
NZ_CP029192.1\|WP_150218131.1\|5414923_5416225_-\|LytR-family-transcriptional-regulator	gnl\|CDD\|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	3.40104e-61

>NZ_CP029192.1|WP_150218138.1|5420498_5421503_+|DNA-3-methyladenine-glycosylase-2-family-protein
MSSRFAPRPTRTTVRGGETAVPGGVPRQATAALTRTWQPPYPLDLGLTLGPLRRGPGDPTFRTTPDGSVWRASRTPLGPGTLRVAARGGSVEAEAWGPGAAWLLDGLPALLGATDDPELFAPRHRLVAMTAHRRPGLRLLRTGLVLESLIPSILEQKITTEEAYRAWRLLVRKYGEPAPGPTPAQARMHVMPDPRTWALIPSWEWHKAGVDNKRSSTILRAVARAGRLEEAASMEPPQAQSRLELIPGIGPWTSAETVQRSNGAPDSVTVGDVHLPGIIGHALADNRDANDEDMLALLAPYEGQRHRAARLILLSGRTPPRRDPKMRKTNIALW
>NZ_CP029192.1|WP_150218137.1|5419356_5420439_+|NTP-transferase-domain-containing-protein
MTEAILLVGGKGTRLRPLTVHTPKPMVPAAGVPFLTHQLARARAAGVDHIVLATSYLAEVFEPYFGDGSALGLHIEYVTETEPLGTGGAIRNVASRLRSGPDEPVLIFNGDILTGLDIRALVDTHETSGADVSLHLTRVDDPRAYGLVPTDATGRVTAFLEKPQTPEEIVTDQINAGAYVFRRSVIDTIPAGRPVSVERETFPDLLASGAHLQGMVDSTYWLDLGTPQAFVRGSADLVLGRAPSPAVPGRCGEHLVMTGADVAPGAKLTGGTVIGENARIGEGARISGSTVLSGAVVEPGAVVSDSLIGAGARIGARSTLSGAVIGDGATVGADNELRDGVRVWCEATLPAGAVRFSSDQ
>NZ_CP029192.1|WP_150218135.1|5417816_5419229_+|peptidoglycan-recognition-protein
MPTIVRMRGFLASSIGVTCAAALALPLTLPSSGARAAAPGAPSAAGPATEAVPGSTQSIPLTPLGSDRALGSAGAREQGLARRDVSPFSLVGVVWNDPEAELHGTVQVRTRATGTTTWSDWQHVETHNHEHAADPGSPERGTGTVRGSTAPLWVGDSDGVEIRVRAEAPPATNRALAPASASASTSSAAPLPEGLRLELVDPGDEPPAQNPGHKAPRAPSMSELSAASSAVNADLAPIGASVIPALTKRQTEDDLIAARGGKAGTKARPFVGPRPRIITRKGWGADEKLREKKFGYTKTVKAAFVHHSATGNYYRCSQSAAVIRSIYRFHVKSSGWRDFGYNFAVDKCGNIYEGRAGGVAKPVLGAHTLGFNTNSMGIAVLGTYSYSNPPKAAVNAIARLTAWKLGLYGANPRGTTYLKSGGGNLYKKGKNVRLRVISGHRDGFATECPGSRLYKKLGTARSTSARFQGR
>NZ_CP029192.1|WP_150218133.1|5416917_5417697_-|TIGR03089-family-protein
MNANDRTPADLLRSALASDPGRPLVTFYDDATGERVELSVATFANWVAKTANLLQGDLSAEPGDRAVLLLPAHWQTAVWLLACSSVGVVADVGGDPASADLVVSGPDSLDAARACSGERVALALRPLGGRFPQPPDGFADYAVEVPGQGDQFAPYAPVDPDEVSLVVDGVELTGAEVVARAREDAGRLGDGGGGDGAGGDTGVRVLSGLSYGTWDGLSAGLYAALAGGGSVVLCRHLERLSEGGLEKRVGDERVGVVRR
>NZ_CP029192.1|WP_150218131.1|5414923_5416225_-|LytR-family-transcriptional-regulator
MGEDAGSHSGGGPSGTGEGGTPYGPGVGASASGVGVGRRQRRWVRWCAVGVAVVVLGAGGLGWAAYQKLNGNITTDTDAAAELARYEKERPTPLVQDAQNILLLGSDTRAGQGNRKYGRDPGTQRSDTTILLHLAADRQSATAVSIPRDLMVNIPGCRKPDGSRTRAQFAQFNWAFEFGGTACTIRTVEKLTDIRVDHHMVVDFAGFKDMVDAVDGVQVCLKAPIDDSDAHVKLAPGLRTLNGEQALGFVRARKSLGNGSDTDRMDRQQEFLGALVNKVQSNDVLLNPTKLYPVLDAATSSLTTDPGLASLRGLYELVRGMRNIPTERVQFLTVPRQSYTYDANRDELVEPAAKELFTRLRTDAPVAVDPRQPAEQARQESSESGYEEGSSEDEEEYDGSGADWSDEKPDDPSQTPSPAPTFRGNTAAGSTCE
>NZ_CP029192.1|WP_150218129.1|5412934_5414698_-|LytR-family-transcriptional-regulator
MDAQGRGRAENIDPADQWVLNPDTGDYELRLSPSAGQSSVPGPRGSSPRQGGRGRSAPGRERSRPDERDERREVPGQRRRRVKEPEPGSGGRRKQNPRKSKGKGKPKSKGKKVMIWTGGTLAFLLVAGCTGGYLYYQHLNDNITSIDDDGAGTGGFSKDRAINILVMGTDKRSGSGNKGYGDEGSAGHADTTILLHVSKDRTNATALSIPRDMIVDIPECPTKQDDGSVKNIPGTQKARFNESLGQSDRTPSCTMRTVKEITGITPDHFMVADFNAVKTLSSAVGGVDVCLAKDIDDPKSHLKLPKGKHTIEGEDALAFVRTRHSVGTGGDLSRIELQQQFLSALMRKLKSNDTLSNPKKMFSLAEAGTEALTVDSKIADIMKLKDLGMELGKLDMKNLSFATVPVIDNPAETVHTTVVPNPTKSEQLFAMMRADQSLTVVKQKEKKEKAAVAARLKGPKADASEVRVDIYNGSGKTGAAQTTLTWLQNTEGVLKSSQLGNAPSDVKKTTLEYAPDQADQARRLADIMGLSGAALKPGKSEKNAQGLPAMKLTLGGDFKGAGVPVDASSKAPKDIDKVEADKVKCAK
>NZ_CP029192.1|WP_150218128.1|5411081_5412833_-|LytR-family-transcriptional-regulator
MRQNSVRKEGARQRAPHASDHGWDEGKDDDTDDGSRGESRAGSRNGSRESAREGSRKGGTRSKKSSKGGGEPPDGSARHRRGAHGGARPPRRKRRVLRWSATILSVLILGTAGAGYLYYQHLNSNLETDDLNLGEHRAPEPTPNAAGQTPLNILLIGSDARDSKANQKLGGAKETFGSPPLADVQMLLHLSADRTNMSVVSMPRDTLLQIPKCTDPDDGKVYPETGPKYMTNESLGRGGPGCTVATWEKLTNIHINHFMMVDFSGVVSMADAIGGVPVCVDRNIHSRDREGHGSGLKLKKGTTEVKGEQALQWLRTRYGFEGGTDISRAKAQHMYMNALVRKLRENTGLTSPNQLRKLAEEATSALTVDDGLGSPRKLYDLGNELKKVSPSRTTMTTMPFDYAGARVVPKPEDAEQLFRLVRDDIPLDGKGKKKPAKEKVSDDPAAADDEIAVQVQNGTRSATEPPVSGRASTVAQLLAGKGFKKATPDSAAALAEEKTVVRFPSADLEGDAQRVAKSLGLPLSAAKKSTDVSGVTLVVGADWREGDAPPKAKKKDDTTPDSADALSGSDKKACMKVDPNFSW
>NZ_CP029192.1|WP_150218126.1|5409973_5411011_+|glycosyltransferase
MNAKSEGQPPAVSVIMPVLNEERHLREAVHAILRQEYAGEMEVVVALGPSTDRTDEIAAELVREDPRVHTVPNPTGRTPAALNAAIKASRHPIVVRVDGHAALSPGYITTAVRLLEETGAMNVGGIMHAEGQNDWEHAVAAAMTSKIGVGNAAFHTGGDAQQAETVYLGVFRREALEQQGGYNEEFIRAQDWELNFRIREAGGMIWFSPELKVSYRPRPSVRALAKQYKDYGRWRHVVARYHEGSINLRYLAPPTAVCAIAAGVVVGAALTPWGFVIPGGYVAAIAAGSVPAGKGLPLKARLRIPVALATMHMSWGWGFLTSPRSLAERVIASRRPAVPGETQRV
>NZ_CP029192.1|WP_150221350.1|5408235_5409606_-|LytR-family-transcriptional-regulator
MRVATGFSVTVLAAAGIGHAVVTGLDTGIKRVDAFRDMKNRPEPGNGMNVLLVGTDGRDKLSPEDKQKYRLGGAPCHCTDTIMIVHISEDRDRASVVSLPRDSYADLPAHTDRNTRQKHHEHPNKINAAYAEGGPNLTVRTVEHMTKVKIDHYLEVDFTSFMKTVDVLGGVEICTARPLQDSHTGLNLAEGTHLMNGGEALQYVRSRYVDGASDLGRMQRQQRFLAALIAKATGSGVLLNPVKFRDVTLTLLGAVRADNGFGTDEILDLGRAMRGFSPSSSEFTTVPLNDKGTTIPGIGSTLVWHPEKSEKLFEALREDRPLAARHGKGGSTMVGVAPQQIRVQVDNGTGDPGLGKRVDAALRKTGFRTSQLPGNIPGAAARPVERTVVAYDPRWDRSAKALATALPGSEMREVKGQGATLKVIAGKDFKEVRRVRAEDVRQGEFGAVTGDQVVCP
>NZ_CP029192.1|WP_150218125.1|5407635_5408184_+|acyl-CoA-thioesterase
MTDQAPNPESEIPGKPTSASRTTLSHIMTHNDTNLLGTVHGGVIMKLVDDAAGAVAGRHSGGPAVTASMDEMVFLEPVRVGDLVHVKAQVNWTGRSSMEVGVRVLAERWNESTPAQQVGSAYLVFAAVDADGKPRTVPPVVPETDRDRRRYQEAQIRRTHRLARRRAIKDLRESRAAEGFDD
>NZ_CP029192.1|WP_150218140.1|5422195_5423542_-|coenzyme-F420-0:L-glutamate-ligase
MTSAATPPSYRVWAVPGLPDVRQGDDLAKLIAAAEPGLADGDVVLVTSKIASKAEGRIVEAADREAAIDAETVRVVARRGTLRIVENRQGLVMAAAGVDASNTPAGTVLLLPADPDASARAVREGLRDALGVDVGVIVTDTFGRPWRAGLTDVAIGAAGVRVLDDLRGSEDAYGNPLGATVVATADELAAAGDLVKGKAAGLPVAVVRGLSRVVVGGDGVDGGDGVDGADAGARALVRDARNDMFRLGTSEAVREAVTRRRTVREFTDEEVDPGAVRRAVAAAVTAPAPHHTTPWRFVLLESAASRVELLDAMRDAWVADLRRDGKSEESIAKRVRRGDVLRKAPYLVVPCLVMDGSHTYGDARRDAAEREMFVVAMGAGVQNFLVALAGERLGSAWVSSTMFCRDVVRDVLGLPGSWDPMGAVAVGHPVDEPSARGGRVVEEFLAVR
>NZ_CP029192.1|WP_150218142.1|5423538_5424495_-|2-phospho-L-lactate-transferase
MRIVVLAGGIGGARFLRGLKKAAPDADITVIGNTGDDIHLFGLKVCPDLDTVMYTLGGGINEEQGWGRTDETFKVKGELAAYGVGPEWFGLGDRDFATHIVRTQMLGAGYPLSAVTEALCERWQPGVRLIPMSDDRIETHVAVTVDGEQKAVHFQEYWVRLRASVDAHAVVPVGAEQAKPAPGVLEAIAEADVVLFPPSNPVVSVGTILAVPGIREAIADAGVPVVGLSPIVGDAPVRGMADKMLAAVGVETGAAAVAEHYGSGLLDGWLVDTVDAGVVERVEEAGIRCRAVPLMMSDLDATAQMAREALALASEVRA
>NZ_CP029192.1|WP_150218143.1|5424529_5425045_-|cupin-domain-containing-protein
MNSDSDLQIAGDILEVPHLLQPAREHPATVAEFVGLARAIAADRSQWEHLVEYDATSRWYHRLRTGPGYEVWLLSWVPGQGSGLHDHGRSSGVLTVLRGELTERTQNGTRALGAGAQRVFAPGYVHEAVNDSLEPAVSLHVYYPGLTEMPMHSAQCAASVAPDATEDVVTA
>NZ_CP029192.1|WP_150221351.1|5425224_5425440_+|hypothetical-protein
MRVIERARFASMPTRTALHTSGVNSVSSMWNMFHLIRLFCQAKGLCRHPAGHMAQQPTLKHRRPSLRGPTG
>NZ_CP029192.1|WP_016642094.1|5425688_5425952_+|WhiB-family-transcriptional-regulator
MTELVQELLVEDADEELGWQERALCAQTDPESFFPEKGGSTREAKKVCLACEVRSECLEYALANDERFGIWGGLSERERRRLKKAAV
>NZ_CP029192.1|WP_150218145.1|5426183_5429909_+|glycosyltransferase
MSVHSHSAAHQEAAAAGFDPSNPPAFPRHIVTAVLVSHDGARWLPDALAGLLGQERPVQNAVAADTGSADDSARLVTEALGADRVLHLARRSGFGTAVDEAVRTAAVLTPEELPYLKRPSGWDPVSRSWRDEAYDMPELPHGEPVQWLWLLHDDCAPDPDALAEMLRVVENEQELGKEVAVVGPKLRGWYDRRQLLEVGVSIANSGRRWTGLDRREQDQGQHDHVRPVLSVSTAGMLIRRDVYEQLGGFDRRLPLMRDDVDLCWRAHAAGHRVLVAPDAVVRHAEASSRERRTVDCVGRTATSPHRVDKAGATYTLLVNARSAVLPWVLFRVVVGTLLRTVAYLVGKAPVQALDEVAGLLATLLRPGRVLAARKQRGKPVPDAGEMRALFPPPGATVRATVEQAAGSLVGRNDAEAPAGAGRHGVVESGPGGDDADFLEIEQFARLKRIARKPGPMLFVVLLFASLIACRALLGSGALAGGALLPAPGDSSDLWARYTDVWHPVGTGGTQGAPPYVALVAGLSTLFLGSTGLAVTVLLVGSVPLAGFAAYFASRPLVTSRLLRAWASIAYAFLPAATGALAGGHIGTAVLAVLLPLIARAGIAASGLAAPHGTRGTWRATWAYTLLLTLATAFTPIVWPIALVLGLALLVVRRGDITAYGLRFLASLGTPLLVLAPWLLTLLPFGFFKEAGLEFGADSATATDLLGASPGGPGTVSGLLLIGIVLAALGALLRGERQRAVRTAWAAALVSLVFAVLSNGSTWAGPATLGYGIALLAAAALGADGARARVAEQSFGWRQPVAALIAFAAAAGPLLVAAGWMIGGADGPLERRDPVQVPAFVAEESGTEDQARTLVLGSESAAQVSYSLVRGSGARLGDAELAAAAADDERLDKIVARLVAGSGADQADQLGGYAVRYVLVRDGAPRQMSRTLDATPGLTRLSQEDGSALWRVDRQVARAAVVPRTGDPEPVAAGPVELHTKIESGDEGRVLRLADSADPGWTATLDGRPLPRTTVDGWAQGFELPTAGGHLDVTYDPPMTHTAWLWAQGALAVVLVVMALPGRRRDVDDDLPDEPVVPAQAVEGEGRRARRLRAQNEQAAQEAGQDVPPPPPSEEALAAVPQQSQSYDGWQAPAPADAEQGAYDAGQPYHGGHYQDGQYPSGTYGQEAYQQDAYQSGAQYDPYASYGGAGGVYGEQQQYGHSFDASYDASYDRHQQHQDPRHQQHQDPTHGTDSERPDGSQQ
>NZ_CP029192.1|WP_150218146.1|5429905_5431396_+|hypothetical-protein
MNRTTQSLIAVVVALGAVTGFAAFGGSEGTDDTGAKSAARLPVERTSLLCPVPSSSDLAETSYTAFTPKAVGAEAKGKAELLPVSKALTDAAKEKDKKAKPFLTQKAPGEPVAGEASGAESPALIGTADGGLAPGWTVQQTTTYAAGSGRGMHGTNCTAPDTDFWFPGASTAKDRSDYIHLTNPDDSAAVVDVELFGPDGEVTSAVGDSIQVQPHSSVPVLLSTLADKKVTNLTMHVTARSGRVAAAVQSSDEKLGGDWLPASADPADSLVLPGIPKDATSVRLVAYAPGADDADLKVQLASPTGTITPAGHESLQVRSGMTAAVDLGDVTKGEAGSLVLSPTDRSVPVVAALRVTRGKGSKQETAFIPATPAVGARATVADNRAKGSTLSLVAPEKTAKVKVTASAGTEGGSPATKTYTVKGGTTLAIADPPKPAGLKGAYALTVEPVSGGPVYGSRMLAAPEEGLPMFTVQPLPDDRGTVEVPKAERDLAVLQK
>NZ_CP029192.1|WP_150221352.1|5431443_5431896_-|metallopeptidase-family-protein
MDDPVQPRAADPRPRRRDRHGRGMRGPVAPPQVPLSTSRGEAFTDLVQDSVERLERRWPQLTEIEFVVLEVPPVGGPDADWQEEVVPLGGTISAAEGRPARVVVYRRPVEIRTKGRDERAHLVHEVVVEQVAELLGLSPESVDPRYGDED
>NZ_CP029192.1|WP_150184425.1|5432158_5432581_+|DUF3499-family-protein
MESRRGPLKSAVPSNAVSPVRRCSRTACGRPAVATLTYVYADSTAVLGPLATYAEPHCYDLCAEHSERLTAPRGWEVVRLADASGPARPSGDDLEALANAVREAARPQERAAEAGGGARRADPMEVARRGHLRVLRSPDN
>NZ_CP029192.1|WP_150218147.1|5432698_5434315_+|L-lactate-permease
MFVQQLEPVADSLGLSALVATLPLLTVLVLLGAVRMKAHRAGLIGLAVAVLVAWLVYGMPLGQTASSAAQGALFGLFPILWIVVNALWVYRMTVRTRHFDILRRSFGRLSDDPRIQALVVAFCFGALLEALAGFGAPVAISAVMLVALGFDPVRAAVVALVANTAPVAFGAMGTPVVTLAQVTGLPLDTVATVVGRQTPLLALVVPLLLVVLVDGRRGLRETWMPALACGFAFAVAQFAASNFVSAQLADIGAALAGAGALMAVPRARRPAAEPVRAAVLTGARSEDLDQDDPRPEVLRAYAPYALIVAVFSLAQIPAVKDFLAKATRTFDWPFLNVADPSGDPVGGNVFSLPLVSTGGTLVLLAGLGTAAVLGVHARVAVREWVATVHELRFAILTVTSVLALAYVMNLSGQAATIGHYVAAAGAGLAFLSPVLGWFGVAVTGSDTSANALFGALQVTAAQQSGLSPELLAAANSSGGVLGKMISPQNLTIACAAVGLAGKEGDLLRKVLPWSLGLLLVMCLIVVGQSTAVLGWMLP

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_CP029192_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_13

5540568-5540769

Orphan

Consensus_repeat	Method
CCGCGCAAGGACGCTCCGACCGCCCGGAGGGTGACCCAGGGACGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_13

>merge|NZ_CP029192|13|5540568-5540769|CRISPRCasFinder
CCGCACCAGAACGCCCCGCCCAGCCGAAGGGCGACCCAGTGGCGCGTGGGCCCGCGCAAGGACGCTCCGACCGCCCGGAGGGTGACCCAGGGACGCGAGGAACTGCGCGAGCAACCCACGACGGCCTGCAGATGACCGGGTCAGGGGCGCGGGGGACCGCGCAAGGACGCTCCGACCGCCCGGAGGGTGACCCAGGGGCGCG

>NZ_CP029192|13|11|5540568-5540769|CRISPRCasFinder
CCGCACCAGAACGCCCCGCCCAGCCGAAGGGCGACCCAGTGGCGCG	TGGGCCCGCGCAAGGACGCTCCGACCGCCCGGAGGGTGACCCAGGGACGCGAGGAACTGCGCGAGCAACCCACGACGGCCTGCAGATGACCGGGTCAGGGGCGCGGGGGA
CCGCGCAAGGACGCTCCGACCGCCCGGAGGGTGACCCAGGGGCGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218231.1\|5533103_5536856_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|274858
NZ_CP029192.1\|WP_150168509.1\|5543573_5544263_+\|cell-division-ATP-binding-protein-FtsE	unknown	unknown	gnl\|CDD\|225438
NZ_CP029192.1\|WP_150218222.1\|5522207_5524451_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|367953
NZ_CP029192.1\|WP_150218228.1\|5529236_5530136_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223472
NZ_CP029192.1\|WP_150218237.1\|5542314_5542977_+\|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl\|CDD\|380203
NZ_CP029192.1\|WP_150218241.1\|5545311_5546508_+\|PDZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|223864
NZ_CP029192.1\|WP_150218236.1\|5540922_5542029_+\|peptide-chain-release-factor-2	unknown	unknown	gnl\|CDD\|234799
NZ_CP029192.1\|WP_150218245.1\|5547994_5548777_+\|collagen-like-protein	unknown	unknown	gnl\|CDD\|237171
NZ_CP029192.1\|WP_150218220.1\|5519486_5520410_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379276
NZ_CP029192.1\|WP_150221360.1\|5549058_5550630_+\|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase	unknown	unknown	gnl\|CDD\|334815
NZ_CP029192.1\|WP_150221359.1\|5530132_5531413_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224096
NZ_CP029192.1\|WP_150218233.1\|5537319_5539005_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP029192.1\|WP_150218226.1\|5526808_5529067_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|367953
NZ_CP029192.1\|WP_150218235.1\|5539221_5540460_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP029192.1\|WP_150218243.1\|5547725_5547998_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218224.1\|5524510_5526763_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|367953
NZ_CP029192.1\|WP_150218239.1\|5544315_5545233_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|225088
NZ_CP029192.1\|WP_150218230.1\|5531486_5532881_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|224567
NZ_CP029192.1\|WP_150168503.1\|5546526_5547048_+\|SsrA-binding-protein-SmpB	unknown	unknown	gnl\|CDD\|376590
NZ_CP029192.1\|WP_150168511.1\|5543153_5543345_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218231.1\|5533103_5536856_-\|FHA-domain-containing-protein	gnl\|CDD\|274858	TIGR03924, T7SS_EccC_a, type VII secretion protein EccCa. This model represents the N-terminal domain or EccCa subunit of the type VII secretion protein EccC as found in the Actinobacteria. Type VII secretion is defined more broadly as including secretion systems for ESAT-6-like proteins in the Firmicutes as well as in the Actinobacteria, but this family does not show close homologs in the Firmicutes. [Protein fate, Protein and peptide secretion and trafficking].	3.2937e-44
NZ_CP029192.1\|WP_150168509.1\|5543573_5544263_+\|cell-division-ATP-binding-protein-FtsE	gnl\|CDD\|225438	COG2884, FtsE, Predicted ATPase involved in cell division [Cell division and chromosome partitioning].	1.36978e-124
NZ_CP029192.1\|WP_150218222.1\|5522207_5524451_-\|glycosyltransferase	gnl\|CDD\|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.08612e-130
NZ_CP029192.1\|WP_150218228.1\|5529236_5530136_-\|ABC-transporter-permease-subunit	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	6.02987e-71
NZ_CP029192.1\|WP_150218237.1\|5542314_5542977_+\|LPXTG-cell-wall-anchor-domain-containing-protein	gnl\|CDD\|380203	NF033201, Vip_LPXTG_Lm, cell invasion LPXTG protein Vip. Vip (Virulence protein), like the LPXTG-type internalins, is an LPXTG-anchored surface protein of the mammalian cell-invading pathogen Listeria monocytogenes, but absent from the related species Listeria innocua. For certain cell types, Vip is required for Listeria's ability to invade. It appears to bind the endoplasmic reticulum (ER) resident chaperone Gp96 as its receptor.	2.86111e-05
NZ_CP029192.1\|WP_150218241.1\|5545311_5546508_+\|PDZ-domain-containing-protein	gnl\|CDD\|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	2.03848e-64
NZ_CP029192.1\|WP_150218236.1\|5540922_5542029_+\|peptide-chain-release-factor-2	gnl\|CDD\|234799	PRK00578, prfB, peptide chain release factor 2; Validated.	0
NZ_CP029192.1\|WP_150218245.1\|5547994_5548777_+\|collagen-like-protein	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	7.04028e-08
NZ_CP029192.1\|WP_150218220.1\|5519486_5520410_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379276	pfam13578, Methyltransf_24, Methyltransferase domain. This family appears to be a methyltransferase domain.	5.20727e-14
NZ_CP029192.1\|WP_150221360.1\|5549058_5550630_+\|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase	gnl\|CDD\|334815	pfam02113, Peptidase_S13, D-Ala-D-Ala carboxypeptidase 3 (S13) family.	4.53333e-119
NZ_CP029192.1\|WP_150221359.1\|5530132_5531413_-\|ABC-transporter-permease-subunit	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.67363e-39
NZ_CP029192.1\|WP_150218233.1\|5537319_5539005_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	1.87622e-103
NZ_CP029192.1\|WP_150218226.1\|5526808_5529067_-\|glycosyltransferase	gnl\|CDD\|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	3.36554e-145
NZ_CP029192.1\|WP_150218235.1\|5539221_5540460_+\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.96375e-85
NZ_CP029192.1\|WP_150218224.1\|5524510_5526763_-\|glycosyltransferase	gnl\|CDD\|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.89418e-146
NZ_CP029192.1\|WP_150218239.1\|5544315_5545233_+\|FtsX-like-permease-family-protein	gnl\|CDD\|225088	COG2177, FtsX, Cell division protein [Cell division and chromosome partitioning].	1.7351e-59
NZ_CP029192.1\|WP_150218230.1\|5531486_5532881_-\|extracellular-solute-binding-protein	gnl\|CDD\|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	1.08877e-26
NZ_CP029192.1\|WP_150168503.1\|5546526_5547048_+\|SsrA-binding-protein-SmpB	gnl\|CDD\|376590	pfam01668, SmpB, SmpB protein.	7.64388e-84

>NZ_CP029192.1|WP_150218235.1|5539221_5540460_+|protein-kinase
MTRKIGSRYTAHQILGRGSAGTVWLGEGPEGPVAIKLLREDLASDQELVGRFVQERTALLSLDHARVVGVHDLVVDGNDLALVMDLVRGTDLRTRLDRERRMAPEAAVAIVADVADGLAAAHAAGIVHRDVKPENVLLDMQGPLGPGGSHPALLTDFGVAKLIDSPRRTRATKIIGTPDYLAPEIIEGLPPRAAVDIYALATVLYELLAGFTPFGGGHPGAVLRRHVTETVVPLPGIPEELWQLLVQCLAKAPASRLRASELASRLRELLPLVAGMPPLDVDEPDTESSQAEEAYEDSAPPEPRETAPRRGAVPLVPGSASADSNRDTHTSMRVPGPDELAGGARGTARAPRASGAARPGSAKNRTSARRRRITLGVAGVVLVAAAGVGTWVATSDDDTPPSEPGNSAPQTP
>NZ_CP029192.1|WP_150218233.1|5537319_5539005_+|protein-kinase
MRPVGSKYLLEEPLGRGATGTVWRARQRETAGAEAAVPGQPGETVAIKVLKEELANDADVVMRFLRERSVLLRLTHENIVRTRDLVVEGDLLALVMDLVDGPDLHRYLRENGPFTPVAAALLTAQIADALAASHADGVVHRDLKPANVLLKQDGQGMHPMLTDFGIARLADSPGLTRTHEFVGTPAYVAPESAEGRPQTSAVDIYGAGILLYELVTGRPPFSGGSALEVLHQHLSAEPRRPSTVPDPLWTVIERCLDKNPDRRPSAENLARGLRAVAEGVGVHSTPAQIAAAEGVGALLMPDPSPAHVPETPGAADPTQVLPNNAGSYDPNAATSVMQSTGGHGSGDADPTSVLPNNRGGNADPTAVMPPVPPNGPGPDPNDPHPWQSQMAAARDRNEQTQYQAHLDPDQDPLRRRPQRQVARPQQQQHPQQYAPQQPRGQRQQRQQYAPAPQQQYQPQHQPQQYAAPPQAPPQQQPAPRPTREPREPRQPRQRSANPMKIPGLGCLKGCLFTIVILFVASWLVWEFSPLQDWIGTTKGYWEQLQDWYDTVSGWMGKIGGN
>NZ_CP029192.1|WP_150218231.1|5533103_5536856_-|FHA-domain-containing-protein
MQIRLTVLGPRSGQTERQDRPAAATDQGATDPRAVGPQGACDVLVTAPAGTALAAVASGLATTVAGSDAPLVLYAGPDRLDAQRCTLGEPPLIDGAVLSLGAPAEPGPELAGAPAQLHVVAGPDAGGVHLLHGGRIQVGRSADADVPLDDPDVSRMHCSVTLTPDGRVTVTDLGSTNGTAVDGKEITDRPVRLSPGSLLRIGESALRLTDGAGGPGSGAGTALATAPDGEGHVRVRPVGTAPPTLVEAAPHGSAAHQAYGPSGWGGTGGEGAYDTGGAQGAHGARSPQGAYGAAHAHGSQSSYGAYGTQPAPVEHGGGTETPVVPHQGTAPDTERTRTGTPARGTTVPRNLRKRGGLSAWARRLTGGRDGGPDHDPYDGPDGPDEYEGYGEYGGHDRHDGPHEAYADGGHAGDRAPGPLGPSPEDLAITAAARTPEAWPDPAALLLTALGPGPRLWERGPGHPEALAVRLGTVDRALPAADGREGLLPAVPVTVGLREAGSLGLAGPRDRLTGLARAVVAQLAALHSPDSLEIVLISTDRARPVAGRTAEWAWLGWLPHLRPAHGQDCRLLLAYDRDQAAARADELIRRLDDHIADSGTGSAGVAATGARTVVVVDGDPGSATLRESTVRLAAEGAQAGIHVVCLAETVAASPSSPVLDTYEAACSVAPAFRACGAVALLSGDVATALRLMRTAGGRPAGHGTVAAVDAVSAAWAERFARALAPLRTDGTAVEGHARVSAPLPRTARLLDELGLARATPASLMARWAAAADDPEALGGRAAAVLGAGPRGPVVADLGAEGPHLLAEGPAGSGRTELLRSVAASLAAAERPDRLGIVLVDGRDGVGAGGAVGRQGTGLGACTDLPHVTTHLVANDPVRMRAFAQSLAAELKRRAELLGRLGFAEWHTQREVSGRMVTQRSQSAAPGATTASTAPVSPRGEVGPTASARSEAPAQAQASAPAEATRPGSSPSVPAARSGAAPSATRPGNSPSAAPARPESTATHPANHPSGNSRPTNAASAASVRPEATHPTTSPSANSHPAASSPAPSVPAQGLDGDLDPAPSATMRLRPASARQRVDPGPPLPRLVVLVDDFDALLAPALGSPGRPAAGSVVRALEAVARDGERLGVHLVATSGRSERVLETELGQRASLRVVLDAVASGPEEPAPGRGELRSPDGRATAFQAGRVTGRIPRTATLRPTVVPLEWERMGDPPARRPVRELGNGPTDLALLASALERAARSVSADQVPSLL
>NZ_CP029192.1|WP_150218230.1|5531486_5532881_-|extracellular-solute-binding-protein
MRSTLRTRRAPLHRRTTARVASAVVAGALAFTVAACGGDDSDDGDKGNKGTDDDTASSLQLPELDGESVSVAAVWGGAERKVFLKVLDEFEKRTGAGVSFVPAQDPIISFLESKVAGGQPPDVAMLPQVGAIEQAVANKWAKPVGTEAQKQLDKNYSKGWQKLGAVDGKQYGVYFKAANKSLVWYNTAVFENAGVKEPKTWDAFMKTAQTVYDSGVPPVSVAGADAWTLTDWFENIYLSQAGPEKYDQLAQHKIKWTDPSVKEALTTLGEVFGTKGFVAGGAKGALQTEFPVSVKQTFTGGDQPKAGMVFEGDMVSLAISETKAKVGTDAKVFAFPAVGDESPAVVGGDAAVALKDSKGAQALLTFLGSPDAAKIWAEAGGFISPNKSLDMAAYPNDVQRNIAKNLIAAGDDIRFDMSDQAPQSFGGTPGKGEWKALQDFLQDPKDVAGTQKALETAAAKAYKD
>NZ_CP029192.1|WP_150221359.1|5530132_5531413_-|ABC-transporter-permease-subunit
MTGTRKAMAVLFLLPALVLLGALVLYPIGYSFFRSFFDDSGDFTAFGNYKTLFTDDSIRTAIKNNAIWVVVAPTVATILGLIFAVLTERVRWGTAFKLVIFMPMAISMLAAGIIFRLVYESDPDRGVANAVMVSVHDTFSESSAFPQAHPSTASPLKNAGGGAFITKEPVKAGTPVVLPLTGVPPDQMPDGAKAARPAEADPQRVTGTAWQDFTRGKGRGKANAPDSTEFGYPGIKIEAVRNGEVVASTEASDDGTFALPKEADGAQLRYPASNFREAYNGIDWLGPTLITPSIIGSYLWMWAGFAMVLIAAGLASVPRELLEAARVDGANEWQVFRRVTVPLLAPVLAVVLVTLMINVLKIFDLVFVIPPGSSKDEANVLAVQLYNSAFLDKDSGVASAIAMLLFLLVIPVMLFNIRRMRREARR
>NZ_CP029192.1|WP_150218228.1|5529236_5530136_-|ABC-transporter-permease-subunit
MTAQTETTARTEIVKARQSVGGRIASLLGSTALRVFLVLVGLFWLVPTIGLLIGSFRTPADMSESGWWKAFSAPSQLTFDNYTTLLKDETITDSILSSIMITVPATLLVVIIGSLAGYAFAWMEFPGRDWWFIGVVALLVVPVQVALVPIADLFGKIGIFETTIGVITFHVAFGLPFAIFLLRNFFAEIPRELLEAARLDGAGELRLFVRVVMPLGAPAIASLGIFQFLWVWNDMLIALIFADSKNPPITVALQQQVRFFGDNVQILAPGAFISMVIPLAVFFAFQRQFVSGVMAGAVK
>NZ_CP029192.1|WP_150218226.1|5526808_5529067_-|glycosyltransferase
MPRFSVIVPAYRVQAYVHECLESVLSQSFTDLELIAVDDCSPDASGAIIDEFAARDARVRAVHLKENVGLGRARNAGMEHATGDYLIFLDSDDTLTPGSLHAISDRIKETGEPDVLIYDYARTFWSGEAIRNQFAAHLTEEGAAPFRLADRPGLLKVLMVAWNKAHRRDFIEREGFTFPPGYYEDTPWTYPLLMTADTMATLDRVCVHYRQRRQGNILGTTSLKHFDIFDQYDRVFAFLDEHPELSAAWRPVMFRRMVDHLSTIFTKRGRLPRGSRAAFLRRARSHYRRHRAPGAPVPARTRLRHGLVRLGSHRTYRGLWAALRLRSRARRSVAYGVRRTKGALLQLHYRVQLRLPVRDRHAVFSSYWGRGYGCNPGALEAAMRELVPGVSTAWIAHPRHHHTIPSATRRLRPGSAAYWTALARSKYLVNNVNFDRRLVKRPGQVLVQTQHGTPLKHMGLDLQERPAAARGMDFAALLRNVDKWDYVLSSNRHSTLVWERVFPAGYTTLEYGYPRNDRYQKATSADVAGLRDRLGIPHGAVAVLYAPTHRDYRRSQLRALDLERMLRALGPRFVVLTRAHHFYGAPLAVGGEQPSGRLIDVSDHPSIESLCLASDALVTDYSSLMFDYANLDRPIVLHADDWEAYEAARGTYFDVRAFPPGAVARSEDELTDIFATGHWAGSRSAQLRRAFRERFCAYDDGRAAERVVRHVVLGEPGGLPSVVPLAERHPVPGGAPRPDRVPFSGLQRSPQL
>NZ_CP029192.1|WP_150218224.1|5524510_5526763_-|glycosyltransferase
MPRFSIIVPTHDVAGRLTGCLASVLGQSFADFEVIAVVDSLDGTAGPSPAIAAEHAARDPRVRRAQSPPDAGLPGARNAGVGAATGDYLLFLDGDDTLTPGTLAALDARLDACDDPDLLFFDHERVHWFEGGEGPVLERLCAGAPRGTFTVAEHAALPDPLVPAFSVAHRRAFVAEHGLVFEPGMFTDALWGLRAVLRAGRIAVLDRVCVRHLLRRQGARHRAPGVHHMDLLDRFGRAMDEAVALDVPAPVLARVFRRFTHELLKAASTPARLPSARLRRRFFRRAARLYRLHRPAGFRAPAGSLGVQHRLLGAGAYGTFCVLRGLKSRVVRAVSLLREVWGKAERRLPGRNAYAAFLRQPVDDGLAVFSAYWGRGYSCNPAAIHAKARELAPHIRTVFLVSGATAAAGLPEGVEGVEIGSRRYWEVMARAKYTFNNVNFEMAVKKRPGTVHVQTQHGTPLKRMGVDQADFPATAAAAGPLGKLLERVDRWDFNVSANRHSTEVWERAYPGAYESLDVGYPRNDAFYRASAADVGALRGRLGVPEGRIAVLYAPTHRDYRTDFAAQLDLPAFCDALGEEFVVLLRAHHLYEGSAGLEEVVRSGKLIDVTEHRSPEEVCLASDALVTDYSSIMFDYANLDRPIVVYADDWDVYRETRGVYFDLLAEPPGVVARTPDELTAAFRSGAWEGPRAGALRAAFRERFCDLDDGLAAERVVRRVLLGEPVERLPPVLPLRDRVPAPAAPRVPQRRP
>NZ_CP029192.1|WP_150218222.1|5522207_5524451_-|glycosyltransferase
MPRFSIIVPVFKVQGFLRACLDSVLTQSFADIEVIAVDDCSPDHCGAIVDEYAAADPRVRAVHLAENAGLGGARNAGVTYATGDYLLFLDSDDSYTPGALAAIDERLRVTADPDVLVFDHVRTHWWGQGGRSMTADLLAAAGTDTFDVLGSPQYLHLFLVAWNKAYRRDFFTGHGFTYREGLYEDAPVTYQALVSARRVGCLDRVCVEYRQRRQGAITRTPGRRHFDIFPQYEALFAFLDARPELDAARPLLFERTINHFLTTLPNTERVPAEDRGDFYRMIVDFHRRHRPPGFTPPDDALRLQWRLTASSPYAVFRAAAAAQSVVAAAREKKQRLRREAARRAKRTFTRVQRAHPLDPDLAVYSAFSHRGLLGDPAAVHQAAGLVAPHVRAVWVVHPDVLDRMPRGVDFVLPDTPAYHRVVSRATYFVSNVNWAPGLVKREGQVHVQTHRGTPLKHMGLDLLGRPAATHRLNLRGQLWRADRWDYSLVSGRHAERAWASAYPCRFTSLPTGAPRNDVLVKGDPLRGVAVRRRLGIPDGGTVILYAPTPRDHRKGYEPRIDFERLVRDAGPGVTLLVRLHPQDARAAVRGLQLRDLERRGVLRDVTDEPSVEDLMLASDALVTDYSSLMFDYACLDRPIVVHADDWEVYQVTRGTYFDLLASPPGHVTTSTARLAELFAAGTWRDERSAALRAAFRARFCEYDDGNAAARVVSRVMLGQEYPPPAIPQQDPGLLRDAVSAALSNNTR
>NZ_CP029192.1|WP_150218220.1|5519486_5520410_-|class-I-SAM-dependent-methyltransferase
MTTTSSEADELPRPTTLEEVPGWFWPLDQRLFAWFLGEGAAATPPGDLLEMGCYLGKSTVVMGRFLRPGEKMTVCDLFGADDGYTKEATKAFYQKSLTRRAFEANYTAFHDTLPELVEGRTDLLPGIVDDASCRFVHIDASHMYDDVRDDILTAKNALREDGVLVLDDYRTEHTPGVAAATWEAVFRHGLRPVMLSSNKLYGTWGDPAPLRDALHEALHAMPNCAPEIQHIAGLDVLRASRAKIPAPDLVTSRHPARPARPAPTAAPALPAPRAQAAAPARKPSAVRRLAVDLLPPVVTRAVRKARR
>NZ_CP029192.1|WP_150218236.1|5540922_5542029_+|peptide-chain-release-factor-2
MAVVDVSEELKSLSSTMESIEAVLDLDKMRADIAVLEEQAAAPSLWDDPDAAQKITSKLSHLQAEVRKAEALRGRIDDLSVLFEMAEEEDDPDTRAEAESELESVKKALDEMEVRTLLSGEYDAREAVVTIRAEAGGVDASDFAEKLQRMYLRWAERHGYKTELYETSYAEEAGIKSTTFAVNVPYAYGTLSVEQGTHRLVRISPFDNQGRRQTSFAGVEILPVVEQTDHIEIDESELRVDVYRSSGPGGQGVNTTDSAVRLTHLPTGIVVSCQNERSQIQNKATAMNVLQAKLLERRRQEEQAKMNALKGDGGNSWGNQMRSYVLHPYQMVKDLRTEFEVGNPESVFNGEIDGFLEAGIRWRKQQEK
>NZ_CP029192.1|WP_150218237.1|5542314_5542977_+|LPXTG-cell-wall-anchor-domain-containing-protein
MTKKTRIRVARIAAGAVIAAGASLTAAGAASALDVGVDLGGASAGAHADESGVGVDVDLPGPGDETPPGDDPTIPGPEDPEEPTEEPTEPTEEPTEPTEDPEPTEDPTDPSDPPTSDPTDPGDENGTGGGNGGGGGNDNNPDGGSNPVEQGKGKDSLTDTGSKPVEQGGNNAQPAADKGELAETGATETTFLLIGAATMIAGGIGFRILPRLVGNRGAAA
>NZ_CP029192.1|WP_150168511.1|5543153_5543345_-|hypothetical-protein
MTLDRLVCANCAAPVSEGRCPVCRANRERMQQEGPFAGLNPAALIALLVVLIAAVALLAHQSA
>NZ_CP029192.1|WP_150168509.1|5543573_5544263_+|cell-division-ATP-binding-protein-FtsE
MIRFDNVSKAYPKQSRPALRDVSLEIEKGEFVFLVGSSGSGKSTFLRLVLREERTSHGQVHVLGKDLARLSNWKVPHMRRQLGTVFQDFRLLPNKTVGENVAFAQEVIGKSRGEIRKSVPQVLDLVGLGGKEDRMPGELSGGEQQRVAIARAFVNRPKLLIADEPTGNLDPQTSVGIMKLLDRINRTGTTVVMATHDQQIVDQMRKRVIELEKGRLVRDQSRGVYGYQH
>NZ_CP029192.1|WP_150218239.1|5544315_5545233_+|FtsX-like-permease-family-protein
MRAQFVLSEIGVGLRRNLTMTFAVIVSVALSLALFGGSLLMRDQVSTMKGYWYDKVNVSIFLCNKADAAQDPKCAKGAVTNEQKDQILGDLKKMPVVDKVVHESADEAYKHYKEQFGDSPLSSSLTPDQMQESFRIKLKDPEKYQVVATAFSGRDGVQAVQDQKGYLDNLFGLLNGMNWAAVAVMALMLVVALMLIVNTVRVSAFSRRRETGIMRLVGASSFYIQMPFIMEAAVAGLIGGGLACGMLLVGRYFMIDHGLELSEKINLINFLGWDAVLAKLPLVLAIGLLMPALAAFFALRKYLKV
>NZ_CP029192.1|WP_150218241.1|5545311_5546508_+|PDZ-domain-containing-protein
MSGLDRFAERFPGPRRIRRGATLTLVFASVLVTGAATGSWSDAADDGRNEPPPSVRSDALAAPEGDADTADEAADAAAEAMADGKSGKDAAEEAVSRSGDRWGSVYSPGEFQEFEKALDGAYTGVGLWARRAADGHIEVSKVQQDGPAERAGIREGDRLRSIDGKHVKGRPVTEVLSLLRGGRAGTPVVLGLERGTRAWREKLHRARLSTDSVRVTEASDGAVVIKVDAFTKGSGEAVRTAVREAPEGAGILLDLRGNSGGLVSEAVTATSALVDGGLVATYDVRGEQKALHAERGGDTDRPVVALVDGGTMSAAELLTGALQDRGRAVVVGSRTFGKGSVQMPSRLPDGSVAELTVGHYRTPSGRAVDGRGITPDLEAEDGAEKRAETVLTGLGPPS
>NZ_CP029192.1|WP_150168503.1|5546526_5547048_+|SsrA-binding-protein-SmpB
MAKEKVKRKAAKAAEKAPARKMVAQNKKARHDYHILDTYECGLVLMGTEVKSLRLGRASLVDGFVHIDRGEAWLHNIHVPEYVQGTWTNHSATRKRKLLLHRAEIDKLESKSQETGHTIVPLALYFKDSRVKVEIALAKGKKEYDKRQALKEKQDLRETNRAIEAAKRRQRGA
>NZ_CP029192.1|WP_150218243.1|5547725_5547998_+|hypothetical-protein
MDATVTLFGSVLAALGVLGAAVVAYLGKRGENALMGFSNLTEKLQIERDRLERQVAERDAKLAELSALHVHDQSEIARLLMDNQRLGGTP
>NZ_CP029192.1|WP_150218245.1|5547994_5548777_+|collagen-like-protein
MTQLERLLARRWRTVFLVCVLLALSGAAVILWARIDAGDRRADQFASEADRRGEAVSTLARDVRTLRAQVRAHGDTPAAPDPSDAVDDLPGRVKVPAGAPGTPGQDGKPGEKGARGNGGQRGEAGEQGDAGERGDRGPQGEPGEPGASGEPGEPGEPGAVGQDGRSGDQGQTGPMGPAGPPGADGASGAMGPRGEQGPKGDRGEKGDPGSPCPDGYSLQEPSGDPDALVCRRTNNGPTGPAPALTLLTALPPQRRRLQDH
>NZ_CP029192.1|WP_150221360.1|5549058_5550630_+|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase
MRHWIWPAVLAVAAAGLSAGSPAGADSDRSGLPEAIDTILADPRMEGGVASVVVADSASGDVLYQHRSSGRLMPASNTKLLTSAAAMELLGPGHRFTTDVRTTAQRRGSELRGDLYLRGTGDPTTLAKDYDRLAAKIADSGIKRVTGRLVADDTRFDDKRVGDTWGGDDESSYYAAQISALSVAPDTDYDTGTVIVEVEPGARAGAKPRVRVTPKTDYVDIDLRATTVARGGADTVAVERQHGKNVITVSGTVPVGGDTTKEWVTVWEPTKYAAAVFRDALTAHGVKVNGPTRAGIATPRDARRLATHDSMPLKDLMIPFMKLSNNMHAESLTKAMGHKATSRPGSWSDGITAIGGYLKTADVDPGKIRQVDGSGLSRKDNVAAEQYIKLLRSAKSEPWFADWYTSLPVACDPDKFVGGTLRTRMCGTPAALNVHAKTGSLTGASALSGYVKDKNGRELVFSIILNNYLPSSVKALEDAIVVTLASSTEDRAVPVTPRSTRAAERDGGAGAELECSWRKPARC

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_CP029192_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_14

5591500-5591591

Orphan

Consensus_repeat	Method
CTGCTGTAGCTGCTCTTGAACCACTCCAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_14

>merge|NZ_CP029192|14|5591500-5591591|CRISPRCasFinder
CTGCTGTAGCTGCTCTTGAACCACTCCAGGGCGACCTCCACGCACGAGTCCCCTTCGTTGCCACTGCTGTAGCTGCTCTTGAACCACTCCAG

>NZ_CP029192|14|12|5591500-5591591|CRISPRCasFinder
CTGCTGTAGCTGCTCTTGAACCACTCCAG	GGCGACCTCCACGCACGAGTCCCCTTCGTTGCCA
CTGCTGTAGCTGCTCTTGAACCACTCCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150221367.1\|5594732_5595605_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224095
NZ_CP029192.1\|WP_055568198.1\|5586834_5587476_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|224332
NZ_CP029192.1\|WP_150218294.1\|5589729_5591274_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|341045
NZ_CP029192.1\|WP_150218307.1\|5599451_5600963_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP029192.1\|WP_150218293.1\|5587792_5589592_-\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223989
NZ_CP029192.1\|WP_150218300.1\|5593086_5593617_-\|DUF664-domain-containing-protein	unknown	unknown	gnl\|CDD\|368218
NZ_CP029192.1\|WP_150218289.1\|5585791_5586001_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218284.1\|5582407_5583835_-\|SidA/IucD/PvdA-family-monooxygenase	unknown	unknown	gnl\|CDD\|226906
NZ_CP029192.1\|WP_150221365.1\|5591623_5592400_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP029192.1\|WP_150218304.1\|5597636_5598107_-\|AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224439
NZ_CP029192.1\|WP_150218285.1\|5584006_5585092_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197715
NZ_CP029192.1\|WP_150218302.1\|5593758_5594736_-\|glycine-betaine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270329
NZ_CP029192.1\|WP_150218282.1\|5581343_5581532_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221368.1\|5596928_5597576_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224095
NZ_CP029192.1\|WP_150218287.1\|5585163_5585778_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378968
NZ_CP029192.1\|WP_150221366.1\|5595631_5596909_-\|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224050
NZ_CP029192.1\|WP_150218305.1\|5598228_5599377_+\|4-hydroxyphenylpyruvate-dioxygenase	unknown	unknown	gnl\|CDD\|273528
NZ_CP029192.1\|WP_150218298.1\|5592635_5593085_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP029192.1\|WP_150218291.1\|5585930_5586731_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226011
NZ_CP029192.1\|WP_150221364.1\|5581599_5582097_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|238979

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150221367.1\|5594732_5595605_-\|ABC-transporter-permease-subunit	gnl\|CDD\|224095	COG1174, OpuBB, ABC-type proline/glycine betaine transport systems, permease component [Amino acid transport and metabolism].	1.05503e-60
NZ_CP029192.1\|WP_055568198.1\|5586834_5587476_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	3.452e-30
NZ_CP029192.1\|WP_150218294.1\|5589729_5591274_-\|MFS-transporter	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). 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. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) 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.	1.46993e-26
NZ_CP029192.1\|WP_150218307.1\|5599451_5600963_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	9.31112e-07
NZ_CP029192.1\|WP_150218293.1\|5587792_5589592_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|223989	COG1061, SSL2, DNA or RNA helicases of superfamily II [Transcription / DNA replication, recombination, and repair].	9.64819e-60
NZ_CP029192.1\|WP_150218300.1\|5593086_5593617_-\|DUF664-domain-containing-protein	gnl\|CDD\|368218	pfam04978, DUF664, Protein of unknown function (DUF664). This family is commonly found in Streptomyces coelicolor and is of unknown function. These proteins contain several conserved histidines at their N-terminus that may form a metal binding site.	1.75929e-44
NZ_CP029192.1\|WP_150221368.1\|5596928_5597576_-\|ABC-transporter-permease-subunit	gnl\|CDD\|224095	COG1174, OpuBB, ABC-type proline/glycine betaine transport systems, permease component [Amino acid transport and metabolism].	5.0482e-53
NZ_CP029192.1\|WP_150218284.1\|5582407_5583835_-\|SidA/IucD/PvdA-family-monooxygenase	gnl\|CDD\|226906	COG4529, COG4529, Uncharacterized protein conserved in bacteria [Function unknown].	2.03093e-37
NZ_CP029192.1\|WP_150221365.1\|5591623_5592400_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	8.54015e-06
NZ_CP029192.1\|WP_150218304.1\|5597636_5598107_-\|AsnC-family-transcriptional-regulator	gnl\|CDD\|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	3.47327e-26
NZ_CP029192.1\|WP_150218285.1\|5584006_5585092_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	1.52446e-14
NZ_CP029192.1\|WP_150218302.1\|5593758_5594736_-\|glycine-betaine-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270329	cd13611, PBP2_YehZ, Substrate-binding domain YehZ of an osmoregulated ABC-type transporter; the type 2 periplasmic-binding protein fold. Osmoprotectant binding lipoprotein YehZ of Clostridium sticklandii is predicted to be involved in uptake of compatible solutes such as choline, L-proline and glycine betaine, but the relative substrate preference is not known. To counteract the efflux of water, microorganisms accumulate the compatible solutes for a sustained adjustment to high osmolarity surroundings. YehZ belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	5.63977e-153
NZ_CP029192.1\|WP_150218287.1\|5585163_5585778_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378968	pfam12840, HTH_20, Helix-turn-helix domain. This domain represents a DNA-binding Helix-turn-helix domain found in transcriptional regulatory proteins.	8.16732e-12
NZ_CP029192.1\|WP_150221366.1\|5595631_5596909_-\|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224050	COG1125, OpuBA, ABC-type proline/glycine betaine transport systems, ATPase components [Amino acid transport and metabolism].	7.96505e-147
NZ_CP029192.1\|WP_150218305.1\|5598228_5599377_+\|4-hydroxyphenylpyruvate-dioxygenase	gnl\|CDD\|273528	TIGR01263, 4-hydroxyphenylpyruvate_dioxygenase, 4-hydroxyphenylpyruvate dioxygenase. This protein oxidizes 4-hydroxyphenylpyruvate, a tyrosine and phenylalanine catabolite, to homogentisate. Homogentisate can undergo a further non-enzymatic oxidation and polymerization into brown pigments that protect some bacterial species from light. A similar process occurs spontaneously in blood and is hemolytic (see . In some bacterial species, this enzyme has been studied as a hemolysin. [Energy metabolism, Amino acids and amines].	0
NZ_CP029192.1\|WP_150218298.1\|5592635_5593085_+\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	3.08396e-16
NZ_CP029192.1\|WP_150218291.1\|5585930_5586731_-\|hypothetical-protein	gnl\|CDD\|226011	COG3480, SdrC, Predicted secreted protein containing a PDZ domain [Signal transduction mechanisms].	9.1712e-31
NZ_CP029192.1\|WP_150221364.1\|5581599_5582097_+\|AAA-family-ATPase	gnl\|CDD\|238979	cd02021, GntK, Gluconate kinase (GntK) catalyzes the phosphoryl transfer from ATP to gluconate. The resulting product gluconate-6-phoshate is an important precursor of gluconate metabolism. GntK acts as a dimmer composed of two identical subunits.	7.72939e-09

>NZ_CP029192.1|WP_150218294.1|5589729_5591274_-|MFS-transporter
MTDDTDDTGGVLSKPYRALSIGIVSVVLLIAFEATAVGTAMPVAARELDGVSLYAFAFSGYFTTSLFGMVLSGQWADRRGPLGPLATGIALFAAGLLLSGTAGAMWLFIAGRAVQGLGGGLVIVGLYVIVSRAYPEHLRASIMAAFAASWVVPSVVGPLISGTVTEHLGWRWVFVGIPVLVLAPLALALPAIRRTASGPVDPDTPVAAFDWRRIRLALGISLGAGLLQYAGQDLRWLSLLPAAAGGAVLVPAVLGLLPKGTYRAARGLPSVVLLRGVAAGAFITAESFVPLMLVTQRGLSPTMAGLSLAVGGATWALGSYVQSRPRMEPYRSRLVASGMVLVAASILAAPSVLIEAVPVWVVGVAWGFGCFGMGMVIASTSVLLLRLSPPADAGSNSAALQISDGLSNVILLAAGGAAFAALGGGTVGTGHGADAGAAGSHPGAFVAVFLPMAVVALAGAWVGTRLQGPRDSDEAAVPAPDETGLVVTDVVTDVRMDVLSDTTPDVTSDVRTRE
>NZ_CP029192.1|WP_150218293.1|5587792_5589592_-|DEAD/DEAH-box-helicase
MTTTSAAANASHHLSPAFPGRAPWGTANKLRAWQQGAMDRYLQEQPRDFLAVATPGAGKTTFALTLASWLLHHHVVQQVTVVAPTEHLKKQWAEAAARIGIKLDPEYSAGPLSKEYHGVAVTYAGVGVRPMLHRNRSEQRKTLVILDEIHHAGDSKSWGEACLEAFEPATRRLALTGTPFRSDTNPIPFVQYAEGNDGIRRSAADYTYGYGSALGDGVVRPVIFLSYSGNMRWRTKAGDEIAARLGEPMTKDAVSQAWRTALDARGEWMPNVLKAADKRLTEVRKAIPDAGGLVIASDQDSARAYAKLIREITGTKATVVLSDDTGASKRIDDFSASTDRWMVAVRMVSEGVDVPRLAVGVYATTISTPLFFAQAVGRFVRSRRRGETASVFLPTVPDLLTFANEMEVERDHALDKPKKEGEEDPYAESEAEMDEANKQEDEDTGEQEQFSFEALESEAVFDRVLFDGAEFGMQAHPGSEEEQDYLGIPGLLEPDQVQMLLQKRQARQIAHSRKKPDEEADLLELPAERRPVVSHKELLGLRKQLNTMVGAYVHQSGKPHGVIHTELRRTCGGPPSAEATAGQLRQRIEKVQEWATRMK
>NZ_CP029192.1|WP_055568198.1|5586834_5587476_-|helix-turn-helix-domain-containing-protein
MTAETSQTLDRGLRVLKLLADTDHGLTVTELSNKLGVNRTVVYRLLATLEQHALVRRDLGGRARVGLGVLRLGRQVHPLVREAALPALRSLAEDIGATAHLTLVDGSEALAVAVVEPTWTDYHVAYRTGFRHPLDRGAAGRAILAARQGLVTDPGYALTHGELEAGASGAAAPLVGVTGLEGSVGVVMLADSVPERVGPRVVDAAREVADALR
>NZ_CP029192.1|WP_150218291.1|5585930_5586731_-|hypothetical-protein
MFSRLTRPQALALCALPVVALLAVAGLAPLPFAVAQPGGTADVLGKHEGKPVLTVSGVPTRATRGELRMTTIVATGPQMDVYLGDVIDGWFRSDRAVMPKDSVYPVGDDVKEVEKHNLGDMKKSQDAATDAALNYLKANGVDDTAKVKVKADLGKIGGPSAGLFLSLGIIDKLDGDGSGGDLTGGRKIAGTGTITADGKVGPVGGVALKTQAAGRDGATVFLVPKDECEDAQAELPKGLRLVPVTTLKGTVDALRALEKGGKVPSC
>NZ_CP029192.1|WP_150218289.1|5585791_5586001_+|hypothetical-protein
MHPYVHLMLHEERAERLRRAAAPRRTNRHHLRAQLGWRLVELGLRLVSSSGPSRPFPAPAARRPFPSAS
>NZ_CP029192.1|WP_150218287.1|5585163_5585778_+|helix-turn-helix-domain-containing-protein
MTEDDRSGPRPRNVHHLNPRSLRGLAHPLRMRLLSSLRLEGPATASQLAARLGESSGATSYHLRQLAEYGFVEDDPDRGKGRERWWRSAHQGTRTDEDLIRDPNPEVQAALSTLLYEYATQRAQEVTTWIATRHEWPQAWDEAADTSDYTLTLSPAQATELSHKVNALMESYRNTPPPRGTPDVAQVRVHSHIFPTRPAPAEDA
>NZ_CP029192.1|WP_150218285.1|5584006_5585092_+|helix-turn-helix-transcriptional-regulator
MNRSRGALSGLERAADAVELFERASAGLRRVVPFDSAVWRATDPETGLITAPMLVQNLGSGEGCAAYWENELLEETVVPYRELARAVVPAAGLRDFTGDLPARSARYRRLLRGWGMHDELRAVLRIGDRPWGLVSLFRDAEPFRPDEIALVADQSRPLATLLRRFARPPASVPPRTDVPAPGLILFDGRGEAMSINEEARQHLAALPKGPSFPSPLGVRLPIWVIGTALQARAVADGRDHGDARVRIRTTEGRWLVCHASCLTGPGGRPGPVALVIEPPAPADLAVLIAESYGLTARELEITQLVARGMTTAEIAGTLFITPHTVRDRLKTLFAKVGVSSRGELVSRLFTEHYWPQGHPLN
>NZ_CP029192.1|WP_150218284.1|5582407_5583835_-|SidA/IucD/PvdA-family-monooxygenase
MNLDLDLDLDLAVVGGGAAAVALLDALSTRAADRPSPGTLRVFEPSPHLWRGRPYGPDLDVVRVNVPPGISSIRHGDAGHYADWLGERAADHIDPLLGLPVVPRALYGEYLTHTAEKAVAAMAEQGWSVEVVPARVTGAARRGTRLALRTADGREYAAAQVALCVGTGNPPDPYGFTGTPGYIADPYPLARTLDHVPVESDVAVIGSGLTAVDVVVALAARGHRGRISLLSRTGVLPYVWQRPVAGRPPRHLTAERVTELHAARGTVTLADLTDLLRAELADRDGDFEALTAELRATTTTDPARRLPQQLDAVDDPRVGRRTLQSAAHAVGPYAWRLLPEADRARLRHHLRTATAVASPMVPVNASVLMRLLDTGQLTVAPGDIRRTLSTTPPDTVVNAVNPPPQAIPAGAGHLVASLVDTGLGTPHPAGGLLPADPRVHVVGDLSGGGSFIASSIPGVAAQASRAARALRTPLS
>NZ_CP029192.1|WP_150221364.1|5581599_5582097_+|AAA-family-ATPase
MASGKSTVAQALAERLPRAAHVRGDAFRRMIVSGGVPYEGVPGGEGEAQLRLRYRLSASAADACSDAGFTAVVQDVILGEELKAYVELVRTRPAYVVVLAPRPEAVAAREESRGKTGYGAWTVADLDAILRERTPRLGLWLDSGELTVDETVDAILSRLDEARVK
>NZ_CP029192.1|WP_150218282.1|5581343_5581532_+|hypothetical-protein
MVAWGFLALVGGLVLATNVCRAADWFQMMSYQHRMWPKSVTTMRVVGAVFSVAGAFVLLGVL
>NZ_CP029192.1|WP_150221365.1|5591623_5592400_-|helix-turn-helix-domain-containing-protein
MVGNQLKLRREVAGMSVAQFAVAIGYGEDLVRKVERGARIPRPEYLDKVDEVVGAGGFVSAMKKEMREARYPKRVRELAKLEERAAEVAVYASHGVHGLLQTEEHSRVVFRARQPAYSQEEVERFVTARMARQSIFGREPAPSLSFVQEEAALRRPIGGTMVWRQQLERLLEVGELPHVTLQVMPIDCEAHPGLDGDIEVLKFGDGTAVGRSDGAFNGRPVTEPKQLRILELRYGIIRAQALTPRETRTFVERVLGET
>NZ_CP029192.1|WP_150218298.1|5592635_5593085_+|ATP-binding-protein
MNQEISTRAQAPTPTHQFTILLSATRRGARLARLLTREQLRCWRRPSEEAEQIVAELANNAVLHGHVPGRSFRLGLLLSAANTLRIEVTDARADRSPPLHPRRPSPKEESGRGLLLVEALADRWGTDLGTLPPSPCKTIWAEIDVPQST
>NZ_CP029192.1|WP_150218300.1|5593086_5593617_-|DUF664-domain-containing-protein
MPGTDTKSPDERADLLEALDHHRTMLRRTARDLTDEQAGLRTTASELCIGGIIKHVTSVERVWAAFIQDGRAAFGDFTAMTDEDVAQRADEFRMLPGETLAGVLAAYEKVASRTDELVRSLPDLDVSHLLPEAPWWEPGGSWTARRVLLHVISETAQHSGHADIIRESLDGALTMA
>NZ_CP029192.1|WP_150218302.1|5593758_5594736_-|glycine-betaine-ABC-transporter-substrate-binding-protein
MRNLRITARTTVVAAVGGALLAACGLTSGSPMVDDVKPGSIGKGLPLKGVDLTVTSKEFTEQLILGAIMGIAFEAAGADVLDRTGIQGSIGAREAVKGGDADAMYEYTGTAWITYQGNTKPITDPQKQWQAVRDADLKNGVTWLEPATLNNTYALAMNESNAATYKTKTLSDVAALSKSDSKAVTLCVESEFASREDGLPGMQKAYGMKVPSSNITKMDTGIIYTQASKGSCVYGEVFTTDGRIKAMDLTTMEDDKHFFPNYNAAPEINSKSLKEHPEMAEVLAPITKKLNNKVARDLNSKVDVEGQDPHEVAKDWLIEEGFVKE
>NZ_CP029192.1|WP_150221367.1|5594732_5595605_-|ABC-transporter-permease-subunit
MPEPKPKPREATRPQGEHDVKGLAFRDEGEAELEAPPAVLGAKQPRRVTWQKLTFLPAVLAIVLLATWWWFQQADLDSISKNALANGNVWLRLRQHIQLTAISTFFVLIIAIPLGILLTRRRLRKGAPVAMAVANIGQATPAIGLLALLVIWLGIGEKAALIGIIIYAVLPVLSNTIAGLKANDPTLIEAARGIGMSPLGVLSKVELPLAVPLILAGVRTALVLNVGTATLATFGGGGGLGDLITTGMTNQRMPVLMLGSILTIALALLVDWLASLAELVLRPRGLEVDA
>NZ_CP029192.1|WP_150221366.1|5595631_5596909_-|betaine/proline/choline-family-ABC-transporter-ATP-binding-protein
MPNGGATAEGAGRTTATTTSGATIELENLTKRYPGSSEPAVDSVNMEIKAGEIVIFVGPSGCGKSTTLKMINRLIEPTGGRIRINGEDVTDIDPVKLRRKVGYAIQSSGLFPHMTVAQNIALVPKMVGWGKSKIKSRVEEMLDLVGLDPAEFHDRYPRQLSGGQQQRVGVARALAADPPVLLMDEPFGAVDPITRDHLQDELIRLQHELHKTIVFVTHDFDEAIKLGDRIAVLRERSHIAQFDTPEAILTNPADDFVSGFVGAGAALKRLNLTRVRDVEIADIPTVTVDDPLQDIFDKLRGGTTNELLLLDKRGRPYKWLRRGDLMRAKGSLARAGTLVHDTVTRDATLRDALEAVLTDNAGRVAVTGRRGEYTGVVDMETLMNSVHEMLEADRLEAVEHQHELEEQRARLTQHEQEGYGGEAKA
>NZ_CP029192.1|WP_150221368.1|5596928_5597576_-|ABC-transporter-permease-subunit
MNFWDYLGNRHQQLLTDAFQHASAVFQCMVVATLMGVLIGVLTYRSEWAGNLATTTTSTILTVPSLAMIGLLIPIVGLGVAPTVIALTLYGLLPIVRNAIVGLRGVDPSLIDAAKGIGMSRVARLFRVELPIAWPPILTGIRVSTQMLMGIAAIAAYASGPGLGNEIFRGIGSLGSKNALNQVLAGTLGIIVLALLFDAAYVLIGRLTIPRGIRV
>NZ_CP029192.1|WP_150218304.1|5597636_5598107_-|AsnC-family-transcriptional-regulator
MAIDHLDGRLIVLLAREPRIGVLEASRRLGVARGTVQARMDRLQSNGVIRGFGPEVDPSALGYPVTAFATLEIKQGQGADVRAHLASVAEVLELHTITGHGDMLCRLVARSNADLQRVIDRVVGFDGIVRASTAIVMENPVPLRIIPLVEQASEDP
>NZ_CP029192.1|WP_150218305.1|5598228_5599377_+|4-hydroxyphenylpyruvate-dioxygenase
MTETTTHTTPDTAREADPFPVKGMDAVVFAVGNAKQAAHYYSTAFGMKLVAYSGPENGSRETASYVLTNGGARFVFTSVIKPSTDWGHFLTSHVAEHGDGVVDLAIEVPDARAAYAYAVEQGARGITEPYEVKDENGKVVLAAIATYGKTRHTLVERTDYDGPYLPGFEAANPIVEPPAKRTFQAIDHCVGNVELGKMNEWVGFYNKVMGFTNMKEFVGDDIATEYSALMSKVVADGTLKVKFPINEPAIAKKKSQIDEYLEFYGGAGVQHIALATNDIVETVRTMRAAGVQFLDTPDSYYDTLGEWAGETRVPVETLRELKILVDRDEDGYLLQIFTKPVQDRPTVFFEMIERHGSMGFGKGNFKALFEAIEREQEKRGNL
>NZ_CP029192.1|WP_150218307.1|5599451_5600963_-|tetratricopeptide-repeat-protein
MRPSVKRVLIGSVAGSVVLGGVLVLLPADGGGKAKPPALGPAGRAMAAVGTGAPAALPDLAALIGEREAQVRAHPGDEQSWAVLGSAYVARGVRTADFADFPKADRALNTSLRAKPEGNPEALTGLAALANARRDFRSARKWGELAVKQAPKRWTAYPALIDAYSGLGDAKGVGRALESLQELGSGSAVLARSGQVYRDRGWREDANAALTDAAALAVAPAAKAAALNRVAELAWERGEPTVALRHYDAALAADAGHHPSMAGRGRALAALGRSSEALLAYRSALTKHPLPEYALELGELYESLRLVPAAHAQYDALRTLVKQERTRGINKERLLGLFEADHGDADAAVGRLTAEYKRHGSPETADALGWALHRSGESEAGLKLVTKAMDKGPRSALFAFHRGSIERELQYYGAARRHLNEALRINPYFSPLAVPEAERALEALGEPPEGGPAEVYAPEPVRQVSRPAPRLRTPARAQPRTQPRTQPSQRQSAPSATRTAPAR

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_CP029192_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_15

5782367-5782469

Orphan

Consensus_repeat	Method
ATCCGCCGCGAAGCGGCGGGTTCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_15

>merge|NZ_CP029192|15|5782367-5782469|CRISPRCasFinder
ATCCGCCGCGAAGCGGCGGGTTCGGCGCCCCTACCCGGAAAGGGCGGTGCGGGGTGAACGGGCGGGTGGGTGGGAGTGATCCGCCGCGAAGCGGCGGGGTCGG

>NZ_CP029192|15|13|5782367-5782469|CRISPRCasFinder
ATCCGCCGCGAAGCGGCGGGTTCGG	CGCCCCTACCCGGAAAGGGCGGTGCGGGGTGAACGGGCGGGTGGGTGGGAGTG
ATCCGCCGCGAAGCGGCGGGGTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150218564.1\|5785232_5786195_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP029192.1\|WP_150218566.1\|5786244_5786844_-\|LysE-family-translocator	unknown	unknown	gnl\|CDD\|224199
NZ_CP029192.1\|WP_150221389.1\|5780024_5781827_-\|glycoside-hydrolase-family-3-protein	unknown	unknown	gnl\|CDD\|366376
NZ_CP029192.1\|WP_150218562.1\|5784376_5785177_-\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|366542
NZ_CP029192.1\|WP_150218550.1\|5770542_5772231_+\|thiamine-pyrophosphate-binding-protein	unknown	unknown	gnl\|CDD\|223107
NZ_CP029192.1\|WP_150218574.1\|5791995_5792832_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP029192.1\|WP_150218576.1\|5792858_5793395_-\|DUF937-domain-containing-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218545.1\|5766353_5767853_-\|PucR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|377939
NZ_CP029192.1\|WP_150218573.1\|5790838_5791999_+\|DUF993-family-protein	unknown	unknown	gnl\|CDD\|368783
NZ_CP029192.1\|WP_150218547.1\|5768032_5769511_+\|sodium:solute-symporter	unknown	unknown	gnl\|CDD\|271373
NZ_CP029192.1\|WP_150218571.1\|5789690_5790842_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP029192.1\|WP_150218558.1\|5779319_5779946_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218557.1\|5777780_5779238_+\|aminopeptidase	unknown	unknown	gnl\|CDD\|283275
NZ_CP029192.1\|WP_150218569.1\|5788506_5789556_-\|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_CP029192.1\|WP_150218549.1\|5769562_5770546_+\|agmatinase	unknown	unknown	gnl\|CDD\|212538
NZ_CP029192.1\|WP_150218555.1\|5777246_5777654_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150218554.1\|5773408_5777146_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP029192.1\|WP_150218560.1\|5782506_5783403_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176115
NZ_CP029192.1\|WP_150218567.1\|5786873_5788427_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|224089
NZ_CP029192.1\|WP_150218552.1\|5772331_5773270_+\|serine-hydrolase	unknown	unknown	gnl\|CDD\|379138

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150218564.1\|5785232_5786195_-\|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.	1.32482e-13
NZ_CP029192.1\|WP_150218566.1\|5786244_5786844_-\|LysE-family-translocator	gnl\|CDD\|224199	COG1280, RhtB, Putative threonine efflux protein [Amino acid transport and metabolism].	1.16948e-37
NZ_CP029192.1\|WP_150221389.1\|5780024_5781827_-\|glycoside-hydrolase-family-3-protein	gnl\|CDD\|366376	pfam00933, Glyco_hydro_3, Glycosyl hydrolase family 3 N terminal domain.	7.48424e-111
NZ_CP029192.1\|WP_150218562.1\|5784376_5785177_-\|TIM-barrel-protein	gnl\|CDD\|366542	pfam01261, AP_endonuc_2, Xylose isomerase-like TIM barrel. This TIM alpha/beta barrel structure is found in xylose isomerase and in endonuclease IV (EC:3.1.21.2). This domain is also found in the N termini of bacterial myo-inositol catabolism proteins. These are involved in the myo-inositol catabolism pathway, and is required for growth on myo-inositol in Rhizobium leguminosarum bv. viciae.	3.46019e-31
NZ_CP029192.1\|WP_150218550.1\|5770542_5772231_+\|thiamine-pyrophosphate-binding-protein	gnl\|CDD\|223107	COG0028, IlvB, Thiamine pyrophosphate-requiring enzymes [acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase] [Amino acid transport and metabolism / Coenzyme metabolism].	6.57384e-145
NZ_CP029192.1\|WP_150218574.1\|5791995_5792832_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.6438e-38
NZ_CP029192.1\|WP_150218545.1\|5766353_5767853_-\|PucR-family-transcriptional-regulator	gnl\|CDD\|377939	pfam07905, PucR, Purine catabolism regulatory protein-like family. The bacterial proteins found in this family are similar to the purine catabolism regulatory protein expressed by Bacillus subtilis (PucR). PucR is thought to be a transcriptional activator involved in the induction of the purine degradation pathway, and may contain a LysR-like DNA-binding domain. It is similar to LysR-type regulators in that it represses its own expression. The other members of this family are also annotated as being putative regulatory proteins.	4.90242e-25
NZ_CP029192.1\|WP_150218573.1\|5790838_5791999_+\|DUF993-family-protein	gnl\|CDD\|368783	pfam06187, DUF993, Protein of unknown function (DUF993). This family consists of several hypothetical bacterial proteins of unknown function.	0
NZ_CP029192.1\|WP_150218547.1\|5768032_5769511_+\|sodium:solute-symporter	gnl\|CDD\|271373	cd11479, SLC5sbd_u3, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	0
NZ_CP029192.1\|WP_150218571.1\|5789690_5790842_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.65101e-49
NZ_CP029192.1\|WP_150218557.1\|5777780_5779238_+\|aminopeptidase	gnl\|CDD\|283275	pfam05576, Peptidase_S37, PS-10 peptidase S37. These serine proteases have been found in Streptomyces species.	0
NZ_CP029192.1\|WP_150218569.1\|5788506_5789556_-\|LacI-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.85187e-101
NZ_CP029192.1\|WP_150218549.1\|5769562_5770546_+\|agmatinase	gnl\|CDD\|212538	cd11592, Agmatinase_PAH, Agmatinase-like family includes proclavaminic acid amidinohydrolase. This agmatinase subfamily contains bacterial and fungal/metazoan enzymes, including proclavaminic acid amidinohydrolase (PAH, EC 3.5.3.22) and Pseudomonas aeruginosa guanidinobutyrase (GbuA) and guanidinopropionase (GpuA). PAH hydrolyzes amidinoproclavaminate to yield proclavaminate and urea in clavulanic acid biosynthesis. Clavulanic acid is an effective inhibitor of beta-lactamases and is used in combination with amoxicillin to prevent the beta-lactam rings of the antibiotic from hydrolysis and, thus keeping the antibiotic biologically active. GbuA hydrolyzes 4-guanidinobutyrate (4-GB) into 4-aminobutyrate and urea while GpuA hydrolyzes 3-guanidinopropionate (3-GP) into beta-alanine and urea. Mutation studies show that significant variations in two active site loops in these two enzymes may be important for substrate specificity. This subfamily belongs to the ureohydrolase superfamily, which includes arginase, agmatinase, proclavaminate amidinohydrolase, and formiminoglutamase.	9.16257e-165
NZ_CP029192.1\|WP_150218554.1\|5773408_5777146_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	5.20293e-166
NZ_CP029192.1\|WP_150218560.1\|5782506_5783403_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|176115	cd08423, PBP2_LTTR_like_6, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator, contains the type 2 periplasmic binding fold. LysR-transcriptional regulators comprise the largest family of prokaryotic transcription factor. Homologs of some of LTTRs with similar domain organizations are also found in the archaea and eukaryotic organisms. The LTTRs are composed of two functional domains joined by a linker helix involved in oligomerization: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal substrate-binding domain, which is structurally homologous to the type 2 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcriptional repressor undergoes a conformational change upon substrate binding which in turn changes the DNA binding affinity of the repressor. The genes controlled by the LTTRs have diverse functional roles including amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to a name a few. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	8.96781e-65
NZ_CP029192.1\|WP_150218567.1\|5786873_5788427_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	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].	7.87731e-110
NZ_CP029192.1\|WP_150218552.1\|5772331_5773270_+\|serine-hydrolase	gnl\|CDD\|379138	pfam13354, Beta-lactamase2, Beta-lactamase enzyme family. This family is closely related to Beta-lactamase, pfam00144, the serine beta-lactamase-like superfamily, which contains the distantly related pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	2.17192e-14

>NZ_CP029192.1|WP_150221389.1|5780024_5781827_-|glycoside-hydrolase-family-3-protein
MSLEDKVGQLFVMHVYGHTATDPDQADVDTNLKELGVRDAAELIARYRLGGVIYFGWAHNTRSPHQIAELSEGIQKASPTIPVLISVDQEHGAVARIGAPATLLPGAMALGASGSHEHAREAARIAGTELRALGIRQDHAPDADVNVDPANPVIGIRSFGADPDAVAGFVTAQIEGYRSAGIATAAKHFPGHGDTTDDSHTELPHIHHTREEWDRYDAPPFRAAIAAGVDSVMTAHIVVPALDPSGDPATLSHPILTGILREELGYDGVISTDSLAMRGVRTKYGDDRVAVLALKAGADQLLNPPRPDIAWHAVIEAVRNGELTEERIDASVLRVLRMKARVGLLDQVLEGAPGAPAPHAPTPALSVDATVGTPAHLVAADHIADATTTLLVNTDALLPLSPATHPRVLVVGADPRSPSGTTGPPTTVLAGALNSLGFQAVALPTGTAPDEAAIEKAVADAQGRDAVLVATYNITTHTTTKDNTQAANTALDQTPGPHARAHRATDPGDDTATGQTRLVTALKATGLPVIALAIRNPYDVAHLPPVDAALASYCWTDVELRAAARVIAGRTVPQGRLPVPVRRADDPAQVLYPIGHGLTY
>NZ_CP029192.1|WP_150218558.1|5779319_5779946_-|hypothetical-protein
MIACDSGWPRTAGRAVCALLLAVTATLTGCQKSPGSESSPKPSQPSGTSTGFFAVDECSSRGRASFTEVPCGSERAAARVIARYDGKVRQGPACPARTDFVLHISESRPAVDEDGDGEVPQGYACMRNLEAPHPGDPGRGGGPRTVVGDCVYGAGRGEVRETACDGSGERAPEYLVSSAVRERAECPAATRLYVTLGGTRPVGCAVRM
>NZ_CP029192.1|WP_150218557.1|5777780_5779238_+|aminopeptidase
MRKALRWVLSLVVLIGTVGVAGATTGTATAADRTRSSTDRADSTDIADIADIKDRLLAIPGMSLIEEKPYPGYRFFVLNYTQPVDHRHPSKGTFKQRLTVLHKDTSRPTVFYTSGYGVSTAPSRREPTQIVDGNQVSMEYRYFTPSRPQPADWSKLDIWQAASDQHRIHKALKSIYGKKWLATGGSKGGMTATYYERFYPRDMDGVVAYVAPNDVVDKEDSAYDKFLAGVGPRECRTRIQDVQREALVRREPLSAKLAAYAEAEGYTFKTVGTLDKAFEAVVMDLVWGFWQYQPAATACGTIPDAAAATDQEIFDYVDSVGGWSSYTDQGLEPYTPYYYQAGTELGAPTIGQPWLGDLSRYGYQPPRNFVPRDIPMKFKPQAMRDVDRWVRHNAHRMMYVYGEYDPWGAEPFRPARGAKHDTHVFTAPGANHGANVAQLVAADKAKATQRIQAWAGVSSSAGKPLAAYDKKLDRRDVRKEQTLRP
>NZ_CP029192.1|WP_150218555.1|5777246_5777654_+|hypothetical-protein
MSSGRGSGRIRRRLTLGTAVLAAAVLLALAGPGTSSAQAVDGLCAGRKVRTLPFSTGRVDVFKSRGYVCAVAVAKRTGARKSMSVSVKARGGRPARDKGHYSHHAGPVTVHAGHRCVWVKGRISGRGVSSGWILC
>NZ_CP029192.1|WP_150218554.1|5773408_5777146_+|ATP-binding-cassette-domain-containing-protein
MAEQRGWARRLTGYAWRYPKDVVLALGSSLGGMAVMALVPLITKVIIDDVIGQDGEGGTRSMGPWAGALIGAALVVYVLTYIRRYYGGRLALDVQHDLRTEMYGTITKLDGRRQDELSTGQVVGRATSDLQLIQGLLFMLPMTIGNILLFVISLVIMAWLSLPLTLVALAVAPALWVIARRSRSRLHPATWYAQAQAAAVAGVVDGAVSGVRVVKGFGQEEQETGKLREVGRKLFAGRLRTIRLNSRYTPALQAVPMLGQVAMLAVGGWLAVEGDITLGTFVAFSTYLAQLVGPVRMLAMVLTVGQQARAGVERVLELIDTEPSMADGRKELPADAPATVEFDDVSFAYEDDRPVLDGLSFEIRPGETLAVVGSSGSGKSTVSLLLPRFYDVTHGAVLIGGHDVRELTLDSLRSAIGLVPEDSFLFSDTVGANIAYGHPEATREQIETAARAAQAHGFISELPEGYDTKVGEQGLTLSGGQRQRIALARAILTDPRLLVLDDATSAVDARVEHEIHEALRGVMAGRTTLLIAHRRSTLGLADRIAVLDEGRLADLGTHAELEERSALYRRLLTDPDELGGVSPGHALPADLPEDTSVRDELDAEFDAERGITPALWTGDRDARSAKDPALAGMPSTPELLAQVDALPPATDTPGIDEARAVTPEESYGLRRLLAGFGVPLLFSLLLVAVDAGMGLLLPVLIRHGIDEGVSDLALGAVWTASGLALVAVVVQWAAQTGETRMTGRTGERVLYSLRLKIFSQLQRLGLDYYERELTGRIMTRMTTDVDALSTFLQTGLVTAFVSVVTFFGIMVALLVIDVELALVVFATLPPLIVGTYFFRKSSVKAYELARERVSVVNADLQESVAGLRIVQAFRRERAGAERFAENSDSYRQARIRGQWLISVYFPFVQLLSSVAVVAVLIVGAGRVEAGTLTTGALVAYLLYIDLFFAPVQQLSQVFDGYQQASVSLGRIQELLQEPTSTKAADEPLEVLSLRGEIAFEDVDFAYAATGEGDPEEALSDVRLRIPAGQTVAFVGETGAGKSTLVKLVARFYDPTGGRVTVDGTDLRSLDLTSYRHRLGVVPQEAYLFAGTVRDAIAYGRPDATDAQVEAAARAVGAHDMIATLDGGYLHEVSERGRNLSAGQRQLIALARAELVDPDILLLDEATAALDLATEAQVNQATDRIAGKRTTLVVAHRLTTAARADRVVVMDHGRVAEDGTHDELLALDGRYARLWRTFVGEPVEAA
>NZ_CP029192.1|WP_150218552.1|5772331_5773270_+|serine-hydrolase
MTHRTSGISRRARVLSAGLAAGVLVPLGAVATAAPAVAAPAPQVTCSSAQAGLAAKLKKDITAALKNRKGTVAVGLYDRTTKTTCTLRGSTAFDSASVVKATVLAALLWDAKKTERKLTERESDLAYAMITKSDNDATSKLWRQLGTGKINAFLKAAKMTKTVPGSGGYWGLTRINATDEQKLLALITAKNSVLSDNARAYILKLMGKVVSSQRWGTPAGTPSGVSIHVKNGWLQRSTHGWRVHSIGAFKGGGHDYTISVLTHGNSTMNYGVATIQGVAKAIHKDLAPRASAVSTYAPTTTPKEAFVAVPSS
>NZ_CP029192.1|WP_150218550.1|5770542_5772231_+|thiamine-pyrophosphate-binding-protein
MSHDHDIVLRPTAAQTEAALNPPAGRNGGDLVMETLAGLGATTVFGLPGQHALGMFDALRRSSLSYVGFRVENNTGFAADAYGRITGEVAPLLLSTGPGALTSLAALQEAAAGSSPVLAIGSQVPVAGLGGGRHGYLHELRDQQASFRDVVKSVHTVRTASQIPSAVAAAWESALTAPHGPVWVEIPQDVLLAETTLPVVTAMDATPEEVVPRPELTAVAADLLLRAERPAIIAGGGVVRSDASGKLRALAELVNAPVVTTFGGKGAFPWEHPLSLQSWLEDRHTTDFLEDADVLLVVGSGLGELSSNYHTFAPRGRVIQIEADAGKLESNHPALGIHADARTALSALLETIEEPREDPEAPERVSAVLAKVRERIDAQDLTLEQRILAAVREALPDASPSFWDMTILAYWAWSAFDARRPNTMHSAQGAGGLGYGFPAALGAAVADPSQPVLAVSGDGGAMYSIAELATARQYGLNVTWLIVDDGGYGILREYMSEAFGEATATELARPDFVKLAESFGVPGVRSSPETLRDDLAKALAEPGPSVVVLPALLRMFAPTHLD
>NZ_CP029192.1|WP_150218549.1|5769562_5770546_+|agmatinase
MSSNETPRGPVDSSRIPRYAGPATYARLPRLDEVGGRTDIAVVGVPFDTGVSYRPGARFGGNAIREASRLLRPYNPAQDASPFALAQVADAGDIAANPFNINEAVETIEAAADDLLGSGARMMTLGGDHTIALPLLRSVAKKHGPVALLHFDAHLDTWDTYFGAEYTHGTPFRRAVEEGILDTEALSHVGTRGPLYGKKDLTDDEKMGFGIVTSADIYRRGADEVADQLRQRIGDRPLYISIDIDCLDPAHAPGTGTPEAGGMTSRELLEILRGLASCNLVSADVVEVAPAYDHAEITAVAASHTAYELTTIMSRQIAEARGTVSER
>NZ_CP029192.1|WP_150218547.1|5768032_5769511_+|sodium:solute-symporter
MAVDYTVIVVYLAGMLAMGWWGMRRAKSKAEFLVAGRRLGPWMYSGTMAAIVLGGASTIGGVGLGYQYGLSGAWMVFTIGLGLLALSVFFSARIARLKVYTVSEMLDLRYGGRAGVISGVVMWAYTLMLAVTSTIAYATIFDVLFDLNRTVAIIIGGAIVVAYSTLGGMWSITLTDMVQFVVKTIGVLLLLLPIAVVKAGGFGEMKAKLPTEYFDPLGVGGETIFTYVLIYTFGMLIGQDIWQRVFTARSDKVARYGGTVAGTYCLVYAIAGAVIGTAAKAMYPKLPSADAAFATIVKDELPMGVRGLVLAAALAAVMSTSSGALIACATVANNDIWSRLRGAVGKPAGEEHDEVKGNRAFILVMGVAVIVIAIALNDVVEALTVAYNLLVGGLLVPILGGLLWRRGTAPGALAAVVAGGLSVIGLMWWYGILANEPVYYGLLTSLAVYVVVSLATRPTDARVLAAWRERLAGRGAGPGAEQPVAEPAPTPQ
>NZ_CP029192.1|WP_150218545.1|5766353_5767853_-|PucR-family-transcriptional-regulator
MADPTAPPTPPVPLAALLAREDLGLRQLAGPDARAAGTAVQWVHTSEMADPYPYLLGGELLLTAGVHITDPSDAAGDYLDAYVSRIVAAGGAALGFGVAPVHDTVPRALAEACDRHGLPLVEVPRRTTFSGVARAVWRLMAEARHAELRRVTEAQQGLATAAARTDPVPAVLRQLASRLGGTAVLYGPDGTELQSAGRTRETARDALRGLTGVVGRGEPGTPASAADTAGDVHLAAYALGGGRGFVLATATERREPGDHTIAGAAVVLLSLLTGEHQSTSEAARSAALVRLLVGAAPAEVAPLLGAGHWHVVHARVGVGLVAGHTPLAAAALAAALGTALVDPPDAADSVEGAVRLLVPADREPAVTDGWVLGVSAPATATGLSAADAQAARALRRAEATRAPLVRHHANGLAALMAPEEADAHARVLLAPLTDNEALTSTLRTWLSLHGSWDRTAVALGIHRNTVRQRITRCESLLGSDLNDPDIRMELWFALTRTTT
>NZ_CP029192.1|WP_150218560.1|5782506_5783403_-|LysR-family-transcriptional-regulator
MLDLGRLRALHAVSVHGTVGAAATALGYTPSAVSQQIAKLERETRTTLLERRGRGVALTEEALHLADTAQQLLAIVERAETELEERRGVPAGRLTIAAFASAARGLMPSVLADLARRHPSLDTRMTEIDPHLSIDLVAKGAVDMAVAHDWDIAPIPTPPGVEQAVIGDDFCDLVVPHDHRLAGRASVRREELKSERWITQPPGLVCHEWLIRTLREAGCEPDIAHQAEENPTLVALVAAGLGVALIPRLGRGPIPSGAVTVPLAPVPVRRLYALWRAGASRRPAIAETVRTLQLHWAP
>NZ_CP029192.1|WP_150218562.1|5784376_5785177_-|TIM-barrel-protein
MRFAFSTLGVPGLPVPDVLRLATTHGYHGVELRAHPEEPVHPGLGIVERADVAAEFKAAGVEILGIAGYARVAAPGEDGPVLDEVRSLVSLARDLGAPFVRVFPGGGTEQGAAEADATAARRLGTAAGYAADAGVRILLETHDSHRTGADATRILGTVGHRQVGALWDLMHTWLGGESVTETFAALSPYLGYVQVKDIASADDTTPLALGSGVLPLEECVARLSAESWEGWLCWEYEKRWYEDAAPLPELLGPGRELLSRLVSRSG
>NZ_CP029192.1|WP_150218564.1|5785232_5786195_-|GNAT-family-N-acetyltransferase
MATTPIHEMRAFNRFYTNLIGALDYSRHLYVPYTLTESRVLYELARSPRTDAADLRTELSLDAGYLSRLLAKFERDGLVERAPSADDSRRQRITLTARGRDAAELLDERSREAVGSLLADVPPAERSRLASAMRTVREILENGRGQGRGRRRERRPDVTLREPGPGDLGWIVQRNAALYAAEFGWNTDYEGLVARIVADFAQDHDPHLERVWIAEVDGRPAGCVMCVRDEAPGTARLRLLLVEPDARGLGIGDQLVASCVEFARGVGYRELTLWTNDVLESARGIYRRHGFVLVAEKPHRSFGVDLVGQDWLLPLHERPS
>NZ_CP029192.1|WP_150218566.1|5786244_5786844_-|LysE-family-translocator
MEFLLTSLVVCVTPGTGVLFTIAAGLSRGTRAAVTAAVGCTLGVVPHMAAAITGLAALLNTSAIAFQTLKYLGVTYLLYMAWSTWRDKSELTAARESEPRSAGRTILTGVLINILNPKLTLFFFAFLPQFVSADEPYALLRMTELSVCFMLITFVVFVAYGRFAAAMRHHVISRPRVVTRLRRVFAAAFAALGARLAFL
>NZ_CP029192.1|WP_150218567.1|5786873_5788427_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MNRSIGSPPHRSITSVSTAPPVPAATSVPTAGGGGVSDFLQLDTGDAPRGGLADWLARRIRDAIADGRLPVGGRLPATRTLAADLRVSRGVVTEAYRRLTEDGHVAGRGRGGTVVVAVPHAPGPGPEASTPPRTGAHDGNVDLFAAPHDDLGVFDAIRAAPARIDLSPGLPDLAAFPRAAWLRAERSVLAGLAPSDFGYGDPRGTPALRTAVAHWLSRNRGIRADPGDVMIVNGTAQALRLLVDVLHADGVREVAVEEPGSLGVRQHLRPLGTPPVPVDAHGVRVDALRASGARAVLLTPAHQFPTGVVLGGERRRELMKWARDGGLVIEDDYDAEHRYDRPAVPALRALLPEHVCYAGSVSKLLAPALRLGWLLAPPAYRDALLDAKRLTDLGTAALPQLVLAHLMESGDLERHLRLIRRHHRRRRDAMIAAIRTHLPTAVVHGAAAGLHLTITFREGAYEGSDAALATAALEQGVKTHPLSWHTQLPHAPGLVLGYAASTPTEIAQGVSVLGGLL
>NZ_CP029192.1|WP_150218569.1|5788506_5789556_-|LacI-family-DNA-binding-transcriptional-regulator
MTVTLADVAARAQVSPATVSRVLNGNYPVAAATRERVLRAVDELDYVLNGPASALAAATSDLVGILVNDIADPFFGIMAGAVQSEIGGPGGRAGGERMAVVCNTGGSPERELTYLTLLQRQRAAAVILTGGAIEDAEHAEAISGKLRRLTEAGTRVVLCGRPPSPDTDAVALTFDNRGGGRQLTEHLVSLGHRRIGYIAGPEERTTTRHRLEGHRAALAARGVPDDPALTVHGPYDRRSGYDATEELLRRAPDLTAVVAANDTVALGACAALRDKGLRIPADVSVAGFDDLPFSIDAVPALTTVRLPLHEAGARAGRIAMSKEKPPPGGVATVHGELMVRGSTAGPRGT
>NZ_CP029192.1|WP_150218571.1|5789690_5790842_+|Gfo/Idh/MocA-family-oxidoreductase
MTRKTVRIAMNGVTGRMGHHQHLVRSILALREQGGLDLGDGTVLWPEPVLVGRREHALRALAEQHGLDQYSTDLDAVLADPAVDIYFDAQVTSAREDALKRAIAAGKHIYTEKPTATGLDAALGLARLAEAAGIKHGVVQDKLFLPGLRKLKRLIDGGFFGRILSVRGEFGYWVFEGDWQPAQRPSWNYRSEDGGGIVVDMFPHWEYVLHELFGRVRTVQALTATHVPQRWDERGKPYDATADDAAYGIFELDGGAVAQINSSWTVRVNRDELVEFQVDGTEGSAVAGLRNCRVQHRSTTPKPVWNPDLPATHSFRDQWQEVPDNGDFDNGFKAQWELFLKHVYADGPYHWDLLAGARGVQLAELGLKSSAEGRRIDVPEIAL
>NZ_CP029192.1|WP_150218573.1|5790838_5791999_+|DUF993-family-protein
MTTLLLPVAGGGTRAYTPSAEPPPTAVGGPPLASRTVFSAAHVVADPFADVSPDGPAAVDWDATLAFRRHLWSHGLGVAEAMDTAQRGMGLDWAGAAELIRRSAAEAKAAGGRIACGVGTDQLTGPASLPEVRSAYEEQLALVDAAGAQPILMASRALAAAATSPDAYLETYGHLLRQAREPVILHWLGPMFDPALEGYWGAADLDAATETFLEVIAAHPDKVDGIKVSLLDADREIALRRRLPDGVRCYTGDDFNYPELIAGDDHGFSHALLGIFDPLGPLAAEAVRALDTGDVKRFRALLDPTVELSRHLFQAPTRYYKTGVVLLAWLAGHQTHFTMVGGLQSARSLPHLARAYELADGLGLFPDPALAAHRMRSLLTVHGVPQ
>NZ_CP029192.1|WP_150218574.1|5791995_5792832_+|TIM-barrel-protein
MTEQVPSSRLSVNQETIKQWSLPELAEGCAKEGVGAVGLWRAPVQEHGVERTARLMRDTGLTVTSLCRGGFLTDIDEAARARALDDNRAAVDEAAALGTDTLVLVSGGLPAGSKDLAGARERIADALAVLGPYAEERGVRLAIEPLHPMFASDRCVVSTLGQALDLAERFPAHQVGVVVDTYHVWWDDQAPAQIARAGRGGRLHAFQLADWITPLPAGVLLGRGQVGDGCIDFRAFRAAVDGAGYRGPIEVEIFNEELWARDGREVLRETADRFRAHA
>NZ_CP029192.1|WP_150218576.1|5792858_5793395_-|DUF937-domain-containing-protein
MTDDSQTSEPRSFEQDVLDELGDDRLQEIAGLLDTDASGAQDVVGTTVSALSGDIQGRAADPAEADEVRQAFDEVGPADPTLQGVATLGGLGGLAGGGMMAGMLAKMSRPVANAVSKKTGIPAAKVTRVIEMLIPVVLAVLSKRAARTKGPGGAPSGSAPSSGGGLGDLLGQILGGKK

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_CP029192_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_16

6954364-6954516

Orphan

Consensus_repeat	Method
CCGCGGGCGTGACGACCGGGG	CRT

3 spacers

The CRISPR arrays of NZ_CP029192_16

>merge|NZ_CP029192|16|6954364-6954516|CRT
CCGCGGGCGTGACGACCGGGGTCGCGACGACCGCGGGCGCGGGCCGCGTCGTGACGACCGCGGCGGGCGGCCCGGTGGTGGCGGGTTCCGCGGGCGTGACGACCGGCGTGACGGCGACCGCGGTGGATACCGCGGCGGGCGTGACGACCGGGA

>NZ_CP029192|16|2|6954364-6954516|CRT
CCGCGGGCGTGACGACCGGGG	TCGCGACGACCGCGGGCGCGG
GCCGCGTCGTGACGACCGCGG	CGGGCGGCCCGGTGGTGGCGGGTT
CCGCGGGCGTGACGACCGGCG	TGACGGCGACCGCGGTGGATACCG
CGGCGGGCGTGACGACCGGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150219438.1\|6961948_6962782_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224045
NZ_CP029192.1\|WP_055569440.1\|6943964_6944903_+\|SPFH/Band-7/PHB-domain-protein	unknown	unknown	gnl\|CDD\|223407
NZ_CP029192.1\|WP_150183357.1\|6944981_6945488_-\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|224321
NZ_CP029192.1\|WP_150183359.1\|6942585_6943383_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224044
NZ_CP029192.1\|WP_150219426.1\|6941366_6941615_+\|DUF320-domain-containing-protein	unknown	unknown	gnl\|CDD\|367652
NZ_CP029192.1\|WP_150219435.1\|6958718_6959765_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|238566
NZ_CP029192.1\|WP_150219425.1\|6941044_6941290_+\|DUF320-domain-containing-protein	unknown	unknown	gnl\|CDD\|367652
NZ_CP029192.1\|WP_150219436.1\|6959818_6960862_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl\|CDD\|182464
NZ_CP029192.1\|WP_150219437.1\|6960858_6961887_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl\|CDD\|227119
NZ_CP029192.1\|WP_150219428.1\|6943428_6943857_+\|NfeD-family-protein	unknown	unknown	gnl\|CDD\|224501
NZ_CP029192.1\|WP_150219434.1\|6957879_6958722_-\|siderophore-interacting-protein	unknown	unknown	gnl\|CDD\|99790
NZ_CP029192.1\|WP_150219430.1\|6946242_6947025_-\|sporulation-protein	unknown	unknown	gnl\|CDD\|369195
NZ_CP029192.1\|WP_150219431.1\|6947186_6947828_+\|DNA-3-methyladenine-glycosylase	unknown	unknown	gnl\|CDD\|234840
NZ_CP029192.1\|WP_150219433.1\|6956737_6957793_+\|HAD-hydrolase-like-protein	unknown	unknown	gnl\|CDD\|319832
NZ_CP029192.1\|WP_150219439.1\|6962765_6963113_-\|sterol-binding-protein	unknown	unknown	gnl\|CDD\|379708
NZ_CP029192.1\|WP_150219427.1\|6941675_6942464_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150219432.1\|6955366_6956665_-\|DUF1015-family-protein	unknown	unknown	gnl\|CDD\|377633
NZ_CP029192.1\|WP_150219440.1\|6963155_6963470_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150221494.1\|6954592_6955312_+\|tetratricopeptide-repeat-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150219429.1\|6945654_6946194_-\|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	unknown	unknown	gnl\|CDD\|182339

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_055569440.1\|6943964_6944903_+\|SPFH/Band-7/PHB-domain-protein	gnl\|CDD\|223407	COG0330, HflC, Membrane protease subunits, stomatin/prohibitin homologs [Posttranslational modification, protein turnover, chaperones].	6.10907e-67
NZ_CP029192.1\|WP_150183357.1\|6944981_6945488_-\|HNH-endonuclease	gnl\|CDD\|224321	COG1403, McrA, Restriction endonuclease [Defense mechanisms].	1.18497e-18
NZ_CP029192.1\|WP_150219432.1\|6955366_6956665_-\|DUF1015-family-protein	gnl\|CDD\|377633	pfam06245, DUF1015, Protein of unknown function (DUF1015). Family of proteins with unknown function found in archaea and bacteria.	5.49861e-123
NZ_CP029192.1\|WP_150219426.1\|6941366_6941615_+\|DUF320-domain-containing-protein	gnl\|CDD\|367652	pfam03777, DUF320, Small secreted domain (DUF320). Small domain found in a family of secreted streptomyces proteins. It occurs singly or as a pair. Many of the domains have two cysteines that may form a disulphide bridge.	3.72394e-14
NZ_CP029192.1\|WP_150219435.1\|6958718_6959765_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	2.46114e-19
NZ_CP029192.1\|WP_150219425.1\|6941044_6941290_+\|DUF320-domain-containing-protein	gnl\|CDD\|367652	pfam03777, DUF320, Small secreted domain (DUF320). Small domain found in a family of secreted streptomyces proteins. It occurs singly or as a pair. Many of the domains have two cysteines that may form a disulphide bridge.	1.79304e-18
NZ_CP029192.1\|WP_150219436.1\|6959818_6960862_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl\|CDD\|182464	PRK10441, PRK10441, Fe(3+)-siderophore ABC transporter permease.	3.56626e-93
NZ_CP029192.1\|WP_150219437.1\|6960858_6961887_+\|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl\|CDD\|227119	COG4779, FepG, ABC-type enterobactin transport system, permease component [Inorganic ion transport and metabolism].	7.26622e-104
NZ_CP029192.1\|WP_150219428.1\|6943428_6943857_+\|NfeD-family-protein	gnl\|CDD\|224501	COG1585, COG1585, Membrane protein implicated in regulation of membrane protease activity [Posttranslational modification, protein turnover, chaperones / Intracellular trafficking and secretion].	4.0954e-15
NZ_CP029192.1\|WP_150219434.1\|6957879_6958722_-\|siderophore-interacting-protein	gnl\|CDD\|99790	cd06193, siderophore_interacting, Siderophore interacting proteins share the domain structure of the ferredoxin reductase like family. Siderophores are produced in various bacteria (and some plants) to extract iron from hosts. Binding constants are high, so iron can be pilfered from transferrin and lactoferrin for bacterial uptake, contributing to pathogen virulence. Ferredoxin reductase (FNR), an FAD and NAD(P) binding protein, was intially identified as a chloroplast reductase activity, catalyzing the electron transfer from reduced iron-sulfur protein ferredoxin to NADP+ as the final step in the electron transport mechanism of photosystem I. FNR transfers electrons from reduced ferredoxin to FAD (forming FADH2 via a semiquinone intermediate) and then transfers a hydride ion to convert NADP+ to NADPH. FNR has since been shown to utilize a variety of electron acceptors and donors and has a variety of physiological functions including nitrogen assimilation, dinitrogen fixation, steroid hydroxylation, fatty acid metabolism, oxygenase activity, and methane assimilation in a variety of organisms. FNR has an NAD(P)-binding sub-domain of the alpha/beta class and a discrete (usually N-terminal) flavin sub-domain which vary in orientation with respect to the NAD(P) binding domain. The N-terminal moeity may contain a flavin prosthetic group (as in flavoenzymes) or use flavin as a substrate. Because flavins such as FAD can exist in oxidized, semiquinone (one-electron reduced), or fully reduced hydroquinone forms, FNR can interact with one and two electron carriers. FNR has a strong preference for NADP(H) vs NAD(H).	6.61168e-81
NZ_CP029192.1\|WP_150219430.1\|6946242_6947025_-\|sporulation-protein	gnl\|CDD\|369195	pfam07070, Spo0M, SpoOM protein. This family consists of several bacterial SpoOM proteins which are thought to control sporulation in Bacillus subtilis.Spo0M exerts certain negative effects on sporulation and its gene expression is controlled by sigmaH.	1.12264e-110
NZ_CP029192.1\|WP_150219431.1\|6947186_6947828_+\|DNA-3-methyladenine-glycosylase	gnl\|CDD\|234840	PRK00802, PRK00802, DNA-3-methyladenine glycosylase.	3.34491e-87
NZ_CP029192.1\|WP_150219438.1\|6961948_6962782_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224045	COG1120, FepC, ABC-type cobalamin/Fe3+-siderophores transport systems, ATPase components [Inorganic ion transport and metabolism / Coenzyme metabolism].	2.38528e-133
NZ_CP029192.1\|WP_150219439.1\|6962765_6963113_-\|sterol-binding-protein	gnl\|CDD\|379708	pfam14864, Alkyl_sulf_C, Alkyl sulfatase C-terminal. This domain is found at the C-terminus of alkyl sulfatases. Together with the N-terminal catalytic domain, this domain forms a hydrophobic chute and may recruit hydrophobic substrates.	1.14379e-08
NZ_CP029192.1\|WP_150183359.1\|6942585_6943383_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224044	COG1119, ModF, ABC-type molybdenum transport system, ATPase component/photorepair protein PhrA [Inorganic ion transport and metabolism].	2.21978e-93
NZ_CP029192.1\|WP_150219433.1\|6956737_6957793_+\|HAD-hydrolase-like-protein	gnl\|CDD\|319832	cd07530, HAD_Pase_UmpH-like, UmpH/NagD family phosphatase, similar to Escherichia coli UmpH UMP phosphatase/NagD nucleotide phosphatase and Mycobacterium tuberculosis Rv1692 glycerol 3-phosphate phosphatase. Escherichia coli UmpH/NagD is a ribonucleoside tri-, di-, and monophosphatase with a preference for purines, it shows peak activity with UMP and functions in UMP-degradation. It is also an effective phosphatase with AMP, GMP and CMP. Mycobacterium tuberculosis phosphatase, Rv1692 is a glycerol 3-phosphate phosphatase. Rv1692 is the final enzyme involved in glycerophospholipid recycling/catabolism. This subfamily belongs to the UmpH/NagD phosphatase family, and to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	2.84133e-100
NZ_CP029192.1\|WP_150219429.1\|6945654_6946194_-\|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	gnl\|CDD\|182339	PRK10257, PRK10257, putative kinase inhibitor protein; Provisional.	1.64465e-59

>NZ_CP029192.1|WP_150219431.1|6947186_6947828_+|DNA-3-methyladenine-glycosylase
MIASPDRTPLTRDFFDRPVLEVAPDLLGRILVRDSAAGPIEVRLTEVEAYAGEVDPGSHAYRGRTARNSVMFGQGGHMYVYFTYGMWHCMNLVCGPVGKAGAVLLRAGEITEGAEIARKRRLSARNDKELAKGPARLATALDVDRQLDGADVCGDPSSPFSVLTGTPTPPAQVSSGPRTGVAGEGGVHPWRFWVTNDPTVSPYRAHVPRRRRT
>NZ_CP029192.1|WP_150219430.1|6946242_6947025_-|sporulation-protein
MGFKKLLASLGAGGASVETVLAEVNVVPGGVVQGEVRIQGGSVDQEIEGLSVGLQARVEVEGNDQETKQDIEFTKVRLGGAFTLQANQVHAVQFTLEIPWETPVTSIDGQQLRGMNIGVTTELEIARAVDSSDLDPINVHPLPAQQAILDAFIQLGFRFKSADMERGHIRGTRQKLPFYQEIEFFPPQQYRGLNQVELSFVADDREMDVVLEMDKKPGLFSEGSDSFRSFKVGLNDFQGTDWAAYLNEWLSQVGSKRNWF
>NZ_CP029192.1|WP_150219429.1|6945654_6946194_-|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein
MSELKRPPLPHDFHPPVPSFTVTSEDFEPGAVLKDAQVYAAGNTSPQLRWEGFPPETKSFAVTCFDPDAPTGSGFWHWTVFDIPVSATELPGGAGSGKFEGLPEGAVQVRNDFGTKDFGGAAPPAGDRPHRYVFTVYAVDQEKLGPDSDAPPAFVGFNLRFHTLARAQVIAEYAAPAES
>NZ_CP029192.1|WP_150183357.1|6944981_6945488_-|HNH-endonuclease
MRDTLVLNASFEPLSTVSLNRAVVLVLQDKAVVEHAHPGLRVRAAAIDIPVPRVIRLCRYVRVPFRRQAPWSRRGVLVRDRHRCAYCGRRATTVDHVVPRSQGGADSWLNTVASCALDNHRKANRTPEEAGMPLLRQPFEPTPADAMLLSLGRDELASLPEWLAQPAA
>NZ_CP029192.1|WP_055569440.1|6943964_6944903_+|SPFH/Band-7/PHB-domain-protein
MEPIIIVLIILVVLVFIALIKTIQVIPQASAAIVERFGRYTRTLNAGLNIVVPFIDSIRNRIDLREQVVPFPPQPVITQDNLVVNIDTVIYYQVTDARAATYEVASYIQAIEQLTVTTLRNIIGGMDLERTLTSREEINAALRGVLDEATGKWGIRVNRVELKAIEPPTSIQDSMEKQMRADRDKRAAILQAEGVRQSEILRAEGEKQSAILRAEGEAKAAALRAEGEAQAIRTVFESIHAGDPDQKLLSYQYLQMLPKIAEGDANKLWIVPSEIGDALKGLGGALGNFGPLGGGSGGSAPATERREQPPID
>NZ_CP029192.1|WP_150219428.1|6943428_6943857_+|NfeD-family-protein
MDIDAWVWWLIGAAALGIPLVLTAMPELGMLAVGAVAASVTAGLGGGAVLQVVVFAAVSVALIAVVRPIATRHRAGRPELVTGVDALKGRSALVLERVDASGGRIKLAGEIWSARALDTDRAYEAGQEVDVVEIDGATAVVM
>NZ_CP029192.1|WP_150183359.1|6942585_6943383_+|ATP-binding-cassette-domain-containing-protein
MSDVLELEDVSVVREGRALVDQVSWSVKEGERWVILGPNGAGKTTLLNVASSYLYPSTGTATILGETLGKPGTDVFELRPRIGVAGIAMAEKLPKRQTVLQTVLTAAYGMTAGWHEDYEDVDEQRARAFLDRLGMSDYLDRRFGTLSEGERKRTLIARALMTDPELLLLDEPAAGLDLGGREDLVRRLGRLARDPIAPSMIMVTHHVEEIAPGFTHVLMIRQGKVLAAGPLELELTSRNLSLCFGLPLVVDQKNDRWTATGLPLS
>NZ_CP029192.1|WP_150219427.1|6941675_6942464_-|hypothetical-protein
MLSEPRSGRLAAWGNALLAGLVSPDDAVLAMVGDDAVHRVEGLPGESGPVGLTLAMGRLRSQGVTGLRVALPAPGHPLGLSGPPEFNARALEAEEAVVGFGAPYGLVPEVYEAGPDGDVHVGVVWHCLPVREAPPADVPSLGEAERELAEALREATEVLSRLDVAGSGPVAEAALDAYRARAERGRELLAPGYPPRAVRVLELAQRVGLLISLAYENGHGGAVSASEMAARVQALRPVERTARRAQVAAYNSSVEERERGGR
>NZ_CP029192.1|WP_150219426.1|6941366_6941615_+|DUF320-domain-containing-protein
MNNIAKKAALAVVAAGLAAGASAGVASATSDAQADGVATKSPGVGSGNLVQVPVDVPVNATGNSVNVIGVLNPAFANHTVNH
>NZ_CP029192.1|WP_150219425.1|6941044_6941290_+|DUF320-domain-containing-protein
MKNLKKAAAVTMVAGGLVAAGAGMASAHGGAHADGVAKNSPGVVSGNLVQAPVHVPVNVCGNTVTVIGGLNPVFGNVCKNL
>NZ_CP029192.1|WP_150221494.1|6954592_6955312_+|tetratricopeptide-repeat-protein
MQSLPKGLAEDVAKNLVMVAKLIDEEPEQAYAYSRIALRLASRVAAVREAAGFAAYANQKYGEALAEFRAARRMTGSVELWPVMADCERGLGRPEKALEMAGAPEVHKLDKAGQVEMRLVAAGARRDLDQIDAAIVTLQSPELASNSVQPWTARLRYAYADALLAAGREDEAREWFAKAVESDKDGSTDASDRLAELDGVEFVDLDDVDGDDDVDEADAGAGAGAETGVGGDVDGPDKD
>NZ_CP029192.1|WP_150219432.1|6955366_6956665_-|DUF1015-family-protein
MNTAGHNDVTGLDLIPFRGVRYVPERVGSLAAVTSPPYDVVVRPDGLLHLESADPHNIVRLILPQATTPEARNQQAADTLHTWLAEGVLAPDAEPSLYVYEQRNSEILQRGVIGALRLSEAADGIVLPHEGVMPHVVEDRAALMQATSANLEPLLLTYRGDEPDAETETEPDGATAVVERAARREPLLSTTTEDGFHHRLWAVTDPAEIAEIQSDLAHHQALIADGHHRWATNLRLRAEHPSPSAWDYGLVLLVDTARYPLRVRAIHRYLHRLPVSDALAALGDSFHIRTVEGPLDHALEALAEAAAKGNAFVLAGDGAFHLVDHPSPELLARTVPNDHPVAWRTLDATVLHSTLLDHVWRIPDTPDHIAYIHDTAATVEKAERDGGTAILMHPVREEVVRDLARQGVTMPRKSTSFGPKPATGLVLRDLTF
>NZ_CP029192.1|WP_150219433.1|6956737_6957793_+|HAD-hydrolase-like-protein
MSQAASGNADGRVRTCPDGSERALSEVYDTALLDLDGVVYAGGHAIAHAVESLGTAREGGMHLAYVTNNALRTPDAVAEHLTELGIATDGSDVITSAQAAARLVSEQVPQGARVLVIGGEGLRVALRERGLEPVESADDDPVAVVQGYGGPDMAWGRFAEACYAIARGVPWFASNTDLTIPSARGIAPGNGAAVEVVRIATGGEPQVAGKPLPPMHRETILRTGAERPLVVGDRLDTDIEGAFNGEVDSLLVLTGVTDGAQLLAAPPEHRPTYVDADLRGMLTGQPDVTPVDGGGFGCGGWTASVRGEELALDGEGESMDGLRALCATAWTQAGDGTCDLDAGKALSRLGL
>NZ_CP029192.1|WP_150219434.1|6957879_6958722_-|siderophore-interacting-protein
MTDSPDSPYRFFDVDVARAEHLTPAMIRVTFTGADLPRMASAGLDQRVKIFLPHPGQDAPVMPDTTSGDALDWYAAWCDLDPSVRGIMRTYTTRELRRDPHELIIDFAVHGPAPSPADGPATSWARTARPGSRIGVLAPVDEENSAYDFRLPDDTDWLLLAADESALPAVANILATLPTGLPTRVWIEVHDLADRQELPTRADAEIHWLTRVGATADAIRGTDLPEGTPYAWIAGESATVKAVRRHLVADRGHDRKRVSFSGYWRQGTTTDELIDSNETA
>NZ_CP029192.1|WP_150219435.1|6958718_6959765_-|ABC-transporter-substrate-binding-protein
MRAARRSPSPAPNRRRVLLAGGALGLGALLTACGDSGSSASGKNGKGGGGGGSWRFKDDRGKTAATEEHPKNIVAFISAAAALHDYGIECKGVFGPSEPVGGKPNPQAGDLNLKGLTSLGTEWGQFNIEKYAALEPDLLISNMFPAPALWYVPEESTEKIASLAPTVGISVARTSLKEPLKRYTELAASLGADLETERVRAAKARFHRAERTLRKAAEANRGLKVMAMTGTADQMYVAVPDSYCDLNYFKDLGIEFVEGKKSDEWGFWEFLGWENADRYHADLIMIDNRTSALPAKELAKKPTWNKLPAVAAGQTIPWPMEERYSYAGYAPVLERLAAAVEKSKRLKR
>NZ_CP029192.1|WP_150219436.1|6959818_6960862_+|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MLVDSPPESRAETAAAPPGRRAIRSVGLLVALAVLLLVFLASIAVGAKSMSMDQVWHGLFQDTGTYGDVVVGERLARSLLGLLAGVALGLSGAVLQALTRNPLADPGLLGINLGASAAVVSAISFFGVTSLSGYVWFAFTGALLVGVLLYFLGGSRGATPVRLALAGTALSAALYGYLQAVMIMDGAALNKMRFWTVGSLASANMDTIKQVLPFLAIGTVLALSLARPLNAMAMGDDTARALGAHLTRTRVLSMAAATLLCGAATAACGPIVFVGLMVPHMVRSFTGPDMRWILPYSAVLSPVLLLGADVVGRVVARPAELQVGIVTAVIGAPVFIFLVRRRKVAQL
>NZ_CP029192.1|WP_150219437.1|6960858_6961887_+|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MKAIRTRGGLSVRLDVRTAVVIALLVVAALVSGVVLIGTGDFYIPAADVVRTLFGNGDAGQEFIINDLRLPRVLVGLLVGAALGLGGALFQSIARNPLGSPDVLGLGQGSTAGALTMIVLFQGSAVQVAAGALVGGLVTGLAIYLLAWKRGVHGYRLVLVGIGVSAFITAINGYLLTKADFVDAARSVVWMTGSLNGRDWDQVWPLLVLCAVLVPLVLVYGRPLRMLEMGEDVANSLGVRVERTRFVLLGASVLLTAAATAAAGPVSFVALTAPQLARRLTRAPGPNLMPAMFMGATLLIVADWASQRAFGADQLPVGVVTGVLGGVYLLWLLVSQRKAGRI
>NZ_CP029192.1|WP_150219438.1|6961948_6962782_+|ATP-binding-cassette-domain-containing-protein
MNRLIADDVTLGYDQRVIAEKLSVEIPDNSFTVIVGPNACGKSTLLRALSRMLKPSTGRVLLDGNVIQSMPAKKVARTLGLLPQSSVAPDGITVGDLVARGRYPHQGLLRQWSEDDERIVNESMASTGVGELAERYVDELSGGQRQRVWIAMALAQQTPLLLLDEPTTFLDIQHQLDVLDLCAELHEEQGRTLVAVLHDLNHAARYATHLIALRDGAVLAEGAPSEIVTAELVKEAFGIDCQIIDDPETGTPLVVPAARAGRRTAVAAGTSSAKAAT
>NZ_CP029192.1|WP_150219439.1|6962765_6963113_-|sterol-binding-protein
MATMAECRTALDKLSDTLASADGDVRSAAALNRSLSCRITDLDVTFTGRLENGRITVLDSHPGPPREKAEIRLAMTGDDLLAMVDGELNFAKAWASGRVKLEAGFRDLLRLRSLL
>NZ_CP029192.1|WP_150219440.1|6963155_6963470_+|hypothetical-protein
MSDSFAGPGQGEAVEPEHQAPDDPSYDPAAPAPLGVERTPTGNAEVDACLARLGDADHLATDGHIEVYEDVHRGLREALTALDARPGPPAPTGAPTTRSSYDRS

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_CP029192_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP029192_17

7169028-7169151

Orphan

Consensus_repeat	Method
CGATCGCCCTGCGGGCTCGTCCTCAAGCGCCGGACGGGCTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP029192_17

>merge|NZ_CP029192|17|7169028-7169151|CRISPRCasFinder
CGATCGCCCTGCGGGCTCGTCCTCAAGCGCCGGACGGGCTGGATTCTCTTCCGCCCGTCCGGTTTTCGCGTGCGGGTGCAGGCGATCGCCCTGCGGGCTCGTCCTCAAGCGCCGGACAGGCTGG

>NZ_CP029192|17|14|7169028-7169151|CRISPRCasFinder
CGATCGCCCTGCGGGCTCGTCCTCAAGCGCCGGACGGGCTGG	ATTCTCTTCCGCCCGTCCGGTTTTCGCGTGCGGGTGCAGG
CGATCGCCCTGCGGGCTCGTCCTCAAGCGCCGGACAGGCTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP029192.1\|WP_150219582.1\|7158152_7158920_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150219599.1\|7181525_7182299_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|180818
NZ_CP029192.1\|WP_150219593.1\|7176243_7176915_-\|FCD-domain-containing-protein	unknown	unknown	gnl\|CDD\|225097
NZ_CP029192.1\|WP_150221516.1\|7164507_7165509_-\|magnesium/cobalt-transporter-CorA	unknown	unknown	gnl\|CDD\|213364
NZ_CP029192.1\|WP_150219586.1\|7165571_7166258_+\|MSMEG_4193-family-putative-phosphomutase	unknown	unknown	gnl\|CDD\|163560
NZ_CP029192.1\|WP_150219598.1\|7179884_7181516_-\|thiamine-pyrophosphate-binding-protein	unknown	unknown	gnl\|CDD\|180820
NZ_CP029192.1\|WP_150219588.1\|7166885_7167710_+\|SCO1664-family-protein	unknown	unknown	gnl\|CDD\|274813
NZ_CP029192.1\|WP_150219584.1\|7161267_7162248_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|223739
NZ_CP029192.1\|WP_150219592.1\|7175093_7176092_-\|PAC2-family-protein	unknown	unknown	gnl\|CDD\|378251
NZ_CP029192.1\|WP_150219583.1\|7159015_7161271_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273632
NZ_CP029192.1\|WP_150219596.1\|7178649_7178874_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP029192.1\|WP_150219589.1\|7167777_7169007_+\|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase	unknown	unknown	gnl\|CDD\|183518
NZ_CP029192.1\|WP_150219594.1\|7177098_7177653_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP029192.1\|WP_150219595.1\|7177634_7178648_-\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|226985
NZ_CP029192.1\|WP_150165941.1\|7162414_7163470_+\|LLM-class-F420-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|274647
NZ_CP029192.1\|WP_150219591.1\|7173093_7174851_-\|S8-family-serine-peptidase	unknown	unknown	gnl\|CDD\|173792
NZ_CP029192.1\|WP_150219597.1\|7178920_7179871_-\|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|99782
NZ_CP029192.1\|WP_150219590.1\|7169274_7172337_+\|DUF5110-domain-containing-protein	unknown	unknown	gnl\|CDD\|269882
NZ_CP029192.1\|WP_150219585.1\|7163691_7164480_+\|ferritin-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|153097
NZ_CP029192.1\|WP_150219587.1\|7166331_7166922_+\|DUF3090-family-protein	unknown	unknown	gnl\|CDD\|213872

Protein	Function_ID	Function_description	E-value
NZ_CP029192.1\|WP_150219599.1\|7181525_7182299_-\|SDR-family-oxidoreductase	gnl\|CDD\|180818	PRK07062, PRK07062, SDR family oxidoreductase.	1.81965e-120
NZ_CP029192.1\|WP_150219593.1\|7176243_7176915_-\|FCD-domain-containing-protein	gnl\|CDD\|225097	COG2186, FadR, Transcriptional regulators [Transcription].	2.10826e-47
NZ_CP029192.1\|WP_150221516.1\|7164507_7165509_-\|magnesium/cobalt-transporter-CorA	gnl\|CDD\|213364	cd12830, MtCorA-like, Mycobacterium tuberculosis CorA-like subfamily. This bacterial subfamily belongs to the Thermotoga maritima CorA (TmCorA)-like family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subfamily includes the Mg2+ transporter Mycobacterium tuberculosis CorA (which also transports Co2+). Thermotoga maritima CorA forms funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport by a related protein, Saccharomyces cerevisiae Alr1p. Natural variants in this signature sequence may be associated with the transport of different divalent cations. The functional diversity of the MIT superfamily may also be due to minor structural differences regulating gating, substrate selection, and transport.	4.50227e-163
NZ_CP029192.1\|WP_150219586.1\|7165571_7166258_+\|MSMEG_4193-family-putative-phosphomutase	gnl\|CDD\|163560	TIGR03848, MSMEG_4193, probable phosphomutase, MSMEG_4193 family. A three-gene system broadly conserved among the Actinobacteria includes MSMEG_4193 and homologs, a subgroup among the larger phosphoglycerate mutase family protein (pfam00300). Another member of the trio is a probable kinase, related to phosphatidylinositol kinases; that context supports the hypothesis that this protein acts as a phosphomutase.	4.18513e-116
NZ_CP029192.1\|WP_150219598.1\|7179884_7181516_-\|thiamine-pyrophosphate-binding-protein	gnl\|CDD\|180820	PRK07064, PRK07064, thiamine pyrophosphate-binding protein.	0
NZ_CP029192.1\|WP_150219588.1\|7166885_7167710_+\|SCO1664-family-protein	gnl\|CDD\|274813	TIGR03843, Phosphatidylinositol_3-_and_4-kinase, conserved hypothetical protein. This model represents a protein family largely restricted to the Actinobacteria (high-GC Gram-positives), although it is also found in the Chloroflexi. Distant similarity to the phosphatidylinositol 3- and 4-kinase is suggested by the matching of some members to pfam00454.	2.08628e-121
NZ_CP029192.1\|WP_150219584.1\|7161267_7162248_-\|aldo/keto-reductase	gnl\|CDD\|223739	COG0667, Tas, Predicted oxidoreductases (related to aryl-alcohol dehydrogenases) [Energy production and conversion].	2.9069e-100
NZ_CP029192.1\|WP_150219592.1\|7175093_7176092_-\|PAC2-family-protein	gnl\|CDD\|378251	pfam09754, PAC2, PAC2 family. This PAC2 (Proteasome assembly chaperone) family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 247 and 307 amino acids in length. These proteins function as a chaperone for the 26S proteasome. The 26S proteasome mediates ubiquitin-dependent proteolysis in eukaryotic cells. A number of studies including very recent ones have revealed that assembly of its 20S catalytic core particle is an ordered process that involves several conserved proteasome assembly chaperones (PACs). Two heterodimeric chaperones, PAC1-PAC2 and PAC3-PAC4, promote the assembly of rings composed of seven alpha subunits.	1.18249e-50
NZ_CP029192.1\|WP_150219583.1\|7159015_7161271_-\|AAA-family-ATPase	gnl\|CDD\|273632	TIGR01448, recD_rel, helicase, putative, RecD/TraA family. This model describes a family similar to RecD, the exodeoxyribonuclease V alpha chain of TIGR01447. Members of this family, however, are not found in a context of RecB and RecC and are longer by about 200 amino acids at the amino end. Chlamydia muridarum has both a member of this family and a RecD. [Unknown function, Enzymes of unknown specificity].	1.54559e-36
NZ_CP029192.1\|WP_150219589.1\|7167777_7169007_+\|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase	gnl\|CDD\|183518	PRK12418, PRK12418, cysteinyl-tRNA synthetase; Provisional.	0
NZ_CP029192.1\|WP_150219594.1\|7177098_7177653_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.60392e-18
NZ_CP029192.1\|WP_150219595.1\|7177634_7178648_-\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	4.51256e-34
NZ_CP029192.1\|WP_150165941.1\|7162414_7163470_+\|LLM-class-F420-dependent-oxidoreductase	gnl\|CDD\|274647	TIGR03559, F420_Rv3520c, probable F420-dependent oxidoreductase, Rv3520c family. Members of this protein family are predicted to be oxidoreductases dependent on coenzyme F420. The family includes a single member in Mycobacterium tuberculosis (Rv3520c/MT3621) but four in Mycobacterium smegmatis. Prediction that this family is F420-dependent is based primarily on Partial Phylogenetic Profiling vs. F420 biosynthesis. [Unknown function, Enzymes of unknown specificity].	7.16275e-130
NZ_CP029192.1\|WP_150219591.1\|7173093_7174851_-\|S8-family-serine-peptidase	gnl\|CDD\|173792	cd04843, Peptidases_S8_11, Peptidase S8 family domain, uncharacterized subfamily 11. This family is a member of the Peptidases S8 or Subtilases serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	1.06332e-106
NZ_CP029192.1\|WP_150219597.1\|7178920_7179871_-\|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	gnl\|CDD\|99782	cd06185, PDR_like, Phthalate dioxygenase reductase (PDR) is an FMN-dependent reductase that mediates electron transfer from NADH to FMN to an iron sulfur cluster. PDR has an an N-terminal ferrredoxin reductase (FNR)-like NAD(H) binding domain and a C-terminal iron-sulfur [2Fe-2S] cluster domain. Although structurally homologous to FNR, PDR binds FMN rather than FAD in it's FNR-like domain. Electron transfer between pyrimidines and iron-sulfur clusters (Rieske center [2Fe-2S]) or heme groups is mediated by flavins in respiration, photosynthesis, and oxygenase systems. Type I dioxygenase systems, including the hydroxylate phthalate system, have 2 components, a monomeric reductase consisting of a flavin and a 2Fe-2S center and a multimeric oxygenase. In contrast to other Rieske dioxygenases the ferredoxin like domain is C-, not N-terminal.	1.53993e-99
NZ_CP029192.1\|WP_150219590.1\|7169274_7172337_+\|DUF5110-domain-containing-protein	gnl\|CDD\|269882	cd06596, GH31_CPE1046, Clostridium CPE1046-like. CPE1046 is an uncharacterized Clostridium perfringens protein with a glycosyl hydrolase family 31 (GH31) domain. The domain architecture of CPE1046 and its orthologs includes a C-terminal fibronectin type 3 (FN3) domain and a coagulation factor 5/8 type C domain in addition to the GH31 domain. Enzymes of the GH31 family possess a wide range of different hydrolytic activities including alpha-glucosidase (glucoamylase and sucrase-isomaltase), alpha-xylosidase, 6-alpha-glucosyltransferase, 3-alpha-isomaltosyltransferase and alpha-1,4-glucan lyase. 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.	1.00429e-171
NZ_CP029192.1\|WP_150219585.1\|7163691_7164480_+\|ferritin-like-domain-containing-protein	gnl\|CDD\|153097	cd00657, Ferritin_like, Ferritin-like superfamily of diiron-containing four-helix-bundle proteins. Ferritin-like, diiron-carboxylate proteins participate in a range of functions including iron regulation, mono-oxygenation, and reactive radical production. These proteins are characterized by the fact that they catalyze dioxygen-dependent oxidation-hydroxylation reactions within diiron centers; one exception is manganese catalase, which catalyzes peroxide-dependent oxidation-reduction within a dimanganese center. Diiron-carboxylate proteins are further characterized by the presence of duplicate metal ligands, glutamates and histidines (ExxH) and two additional glutamates within a four-helix bundle. Outside of these conserved residues there is little obvious homology. Members include bacterioferritin, ferritin, rubrerythrin, aromatic and alkene monooxygenase hydroxylases (AAMH), ribonucleotide reductase R2 (RNRR2), acyl-ACP-desaturases (Acyl_ACP_Desat), manganese (Mn) catalases, demethoxyubiquinone hydroxylases (DMQH), DNA protecting proteins (DPS), and ubiquinol oxidases (AOX), and the aerobic cyclase system, Fe-containing subunit (ACSF).	0.00155906
NZ_CP029192.1\|WP_150219587.1\|7166331_7166922_+\|DUF3090-family-protein	gnl\|CDD\|213872	TIGR03847, TIGR03847, conserved hypothetical protein. The conserved hypothetical protein described here occurs as part of the trio of uncharacterized proteins common in the Actinobacteria.	8.90672e-85

>NZ_CP029192.1|WP_150219589.1|7167777_7169007_+|cysteine--1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside-ligase
MHAWPASEVPALPGKGRDLRIHDTATGGLVTLDPGPVARIYVCGITPYDATHMGHAATYNAFDLVQRVWLDTKRQVHYVQNVTDVDDPLLERATRDGKDWVELAEGETALFREDMTALRLLPPKHYIGAVEAIPGIVPLVERLRDMGAAYELEGDVYFSVESDTHFGEVSGLDTAAMKLLSAERGGDPERVGKKNPLDPMLWMAAREGEPSWDGGSLGRGRPGWHIECVAIALDHLGMGFDVQGGGSDLAFPHHEMGASHAQALTGEYPFAKAYVHAGMVGLDGAKMSKSKGNLVFVSQLRRDGVDPAAIRLALLAHHYRADWEWTDAVLAEAVERLGRWRAAVSRPDGPSAEALVEEIREALANDLDAPAALAAVDRWAAGQASAGGADEGAPGVVSRAVDALLGVAL
>NZ_CP029192.1|WP_150219588.1|7166885_7167710_+|SCO1664-family-protein
MPAPERIPAGSVTAVDPVTLLTHGELTVRGRIREASNAVLYCTVAYEGQEAACVYKPVAGERPLWDFPDGTLAQREVAAYEVSLATGWDLVPPTVLRDGPHGEGMCQLWIEASGDAELLALVDGDEPGEGWKAVGLAQVDEERTALLVHADDVRLRRLAVLDAVINNSDRKGGHLLPADGRLYGIDHGVTFHAENKLRTLLWGWAGEPLTDEALEALQGLQDGLAEGAGLAGRLAALITAGETEALRARVAALLKSGRHPEPSGEWPAIPWPPV
>NZ_CP029192.1|WP_150219587.1|7166331_7166922_+|DUF3090-family-protein
MSRQVFLYDPPERFVAGTVGLPGRRTFFLQASAGVRVTSVALEKTQVAALAERMEELLDEVVRRSGGNAPVPAVAPSEVSDSAPLDSPVEEEFRVGTMALAWDGEEERMVVEAQALVELDADTEDDLAAAEERLLQDEENGPPMLRVRLTGAQARAFAKRALDVVNAGRPPCPLCSLPLDPEGHVCPRQNGYRRGA
>NZ_CP029192.1|WP_150219586.1|7165571_7166258_+|MSMEG_4193-family-putative-phosphomutase
MPTLILVRHGRSTANTAGLLAGWTPGVALDERGSAQAAALPGRLSALPLSEVVTSPLQRCRETVAPLLAARPGLQAHTDDRIGECDYGDWSGRKLAELADEPLMEVVQRHPSAAAFPGGESMRAMQTRAAEAVREWNARVERDHGEDAVYLMCSHGDIIKSLVAEALGLHLDLFQRISVEPCSVTAIRYTRLRPFLVRLGDTGDFASLAPREEPSGDDATVGGGAGAP
>NZ_CP029192.1|WP_150221516.1|7164507_7165509_-|magnesium/cobalt-transporter-CorA
MIVDCAIYRDGRRTEGPGDLSDALDQARAEGDAFVWIGLHEPTEKEFDRVTQEFGLHPLAVEDALKAHQRPKLEVYDDSVFMVLKPVVYEQDSDTVSSGEVMIFMGDSFVVTVRHGEGAPLGVVRHRLEAEPDVLKHGPTAVLYSIADASVDHYLEVADELQADLEVLEAEVFSPDGGSSSRNTASRIYRFKRQILEFRRATGPLALPVARLSGVGPFSPSVPFVDETAQPFFRDVNDHLTRVNESVEGLDRLVSDILSAHLAQMSVRQNDDMRKISAWAAMAAVPTMIAGVYGMNFDHMPELHWWWTYPAVILLMALLEVVLYRMFKRRGWL
>NZ_CP029192.1|WP_150219585.1|7163691_7164480_+|ferritin-like-domain-containing-protein
MLSARSVFEEILDNDESYRLFCSIAASGEAQGGWENGRIAALVPQSERALAPKIARHGADEDKHGRIFHALLKKRGLQPVDVPHDTDYTMLLEKHGIGLAHDKLKADEPLSVRDVVTYLSHSRVTEQRASEQMRLLLKYFADHPDIGRAVRMISNDEDNHLAYCHEELLRFARAGHGRAIQRTLRECAHAEIRVYRDVSLAVMERMGRILHWPHAKRQLLTAGIHAVYGYERAVGWRRMVSLEMPGRRDALGGPATTATEFA
>NZ_CP029192.1|WP_150165941.1|7162414_7163470_+|LLM-class-F420-dependent-oxidoreductase
MQLGINLGYWGAGMDADNLAVAKEADKLGYAVCWAAEAYGSDAATVLSWVAAQTERIDIGSAIFQIPARQPAMTAMTAATLDSLSGGRFRLGLGVSGPQVSEGWYGVKFDKPLARTREYVEIVRKAMTRERLSYEGEHWTLPLPGGPGKPIKLTVHPQREHIPLYVAAIGPKNLEQTGEIADGALLIFPAAEHLEDTAIRHLRAGREKAGKTMDGFDVVPTVPLAVGEDAQVDALADMFRPYTALYVGGMGSRKQNFYNQLAQRMGYEKEAAEIQDKYLAGDKDGAAAAVPRQLIDSTTLLGSVDRIADRMQAYAAAGVTTLTLAPAGFTLEERLASLRAGTEALERAGLA
>NZ_CP029192.1|WP_150219584.1|7161267_7162248_-|aldo/keto-reductase
MEQRHLGRTGLRVSRIGLGTLTWGHTEENDAADLLKVFWEAGGTLVDTADVYGDGEAEYLIGRLIERLVPRRDLVIATKAGSVPDPERRFDGSRGHLLAALDASLSRLGTDYVDLWQVHAFDPGTPLEETLQALDIAVSSGRARYAGVADFCGWQLAKAATWQLAASGTRTRLASTQMEYSLLQRGVEREVLPAALDLGVGLLPSSPLGRGVLTGKYRHATPADSRGGSDHMAPFVAPYLDETASHIVDAVATAADGLAATPLQVALAWVRDRPGVTAPIIGARNAQQLTAALSVETLSLPDEICRALDDVSAPVHRYPDHDWSTL
>NZ_CP029192.1|WP_150219583.1|7159015_7161271_-|AAA-family-ATPase
MSTEPAAAEDPGAAAAEEAESPGTEEAAPDAEAASDTGESKVEGENAENAENAENTEEAKGEGESAELSETEAEIAAQRELRERIEQRKASKQGPIDAGTKLSGTAADLLAAVRAVESGEKPVASAFREPEPARRPAPSRAPEPVRPQQPAADRAPARETVEAVRAVLAEGGAPPALAEPTAAALGDGADGQLRADPWQLLRVTGVRPEQADGFARALLGAECGPDDERRGRAITVWLLEQAAVAGHTALDAAALSAALGQRAVPDPEAAVQGALAEGDALVFQDALEGTEVPVQRTDDEAARNEESGEDGADAEPERPVRVLIGLERYALAEESLADGLARVINSLPKETDDTAEPEGPDWKGAAARASGSAAELIRAVAGHGLVLHSGGEEARAEPAALVAAAAALGLRVCAAAHSADGRRRLARAAGVEGTAVTVAGLLAGDEGPGRDAEGALALDLLVVLDAPQLDVETAAMLVESLPDGARLVLSGDPGVLWSAGPGRVFADLLSARCCPQVVSRTPDPGPVGELTSGIGIGELNQVEAPGKEVVLVPVRDPAEAIHRTVQLVADSVPRAIGVPAEHTQVITPGHGGAAGTRALNAALKERLNPGPGRFGGFDPDDRVAHVPAPGRTTLGRVVRADAEGLHLECDGAPVVVPQERVEREVRHGWALTAHQATGQRWPAVVVVLPGDAAPALSRPWVYTAFSRAERHLSVVQGVEQALPRAVAERLWKDRTTRLQTLLRPQVPATTA
>NZ_CP029192.1|WP_150219582.1|7158152_7158920_+|hypothetical-protein
MSDAAQPTAAEVRAAAEAVKTALDRHLAAVERRSGEDDPAVYEAFNELAAAAEEYDELLYDRYDEVTPFEIPGSDDALPPYQGPDEANALSVLLRRDYTVVEPQRLLAQAQRVADLEAGGTGGAGSADTVHSALGVLFGEFEPDEISSRHKEFGLEEGDSTLWVTAVDTPAEPGEWLDAPFDQADPHRVVCRFDVSVVFDDELDDEGLDGLDTDVDIDIDPDVPVPVDDTDDTDDAEEDGDGAAGGGSAAWRAGR
>NZ_CP029192.1|WP_150219590.1|7169274_7172337_+|DUF5110-domain-containing-protein
MRSPTRFRPVVAVVLLGLLAVFAGPGGGSAQAAEEPSGTTVGDVTGFDADGSVYQLTAGQVEARVSFVSAETFRIELAPDGKFTDPAGGDIVLPQGKAPRTKWADKGDRYEMRTSEVTLRAYKSPLRFALYRSDGSRVWAESKGLSWTKEGTTQSLARGGDEQFYGGGMQNGRGNTSHRGKKVEVSVDYNWDDGGHPNSVPFYLSSEGYGVFRNTYAPNTYDFGAPVTATAKEQRFDAYYFAGRGSDAAKDVIGQYTKLTGKPFLPPVYGMEIGDADCYLHNANRGERHTLDSLKVADGYVENDMPNGWMLVNDGYGCGYEDLAETAKGLQERDMQLGLWTEDGLDKIAEQVKAGQRVAKLDVAWVGDGYKKALDGCKDAYKGIEDNSDARGFTWAPESWSGAQRCGVQWSGDQSGSWEYIRWQIPTYAGSTMSGLAYTTGDVDGIFGGSPKTYVRDLQWKMFLPVTMTMDGWAASDKQPFRQGEPYTSINRKYLKLHESLLPYLYSYGHEATQTGVGAVRPLALEYPHDPKAATDAAKYEFLTGEDFLVAPVYKDTTTRDGIYLPKGTWTDYWSGRTYQGPTTIDGYSAPLDTLPLFVRGGATVPMWPGGIRSYRDRTSHSPLAWDIYPQGDSSFELYEDDGVTRQHRDGKYATQRAEVRAPHSGAGDVRVRIGASKGTYKGKPGSRAHSFTLHTGDAPSRVELGGHRLPRLSSESAYDRARAGWFYDRDDRGGVVKVKTAALRTDRGFELRLDDTSAVGGAVPGAPATVSVPAGQELGAGTPGKVAVDITAGTRDATGVEATLDVPAGWTAGTAKADRVPAGTTRRVEVALTPAKDADIGEQPLTATVRHRSAGQDRTAVQRFALGVMPKAPVEDTWASDMKWLKSTNGYGPAERDRSNGESGAEDGHTLTLAGRTYEKGIGTHADSVIEVYPGGRCTKFSADVGIDDEINGYGEVAFSVEADGKVLWTSPKVTGASATVPVDVDVRGARHVELKVSDTNGSKSGDHADWAAARFSCA
>NZ_CP029192.1|WP_150219591.1|7173093_7174851_-|S8-family-serine-peptidase
MTEQADPARDPGAGGPGPDGMGFTYREAQQELIVVARPEARLRAGERDVRSASGSDVSALNMFLTDEQLTLEPLFGNEDRLRAAAPSATGGDDVPDLALFYRVRGGDDRPDELRARMAALPGIDTAYVKPGAVPASIDPSPTQPHDLDEATRRRKEGMPATPDFTSRQGYLKPAPEGIDARWAWQRIGGSGEGVTVVDIEGAWQLRHEDLAAKLAGVVVGTPLQDLAWRNHGTAVIGVIGGDRNSLGITGIVPEAVTATASFQPLGTAATIHAAAERLNPGDIILLELHRPGPKFDFGPRDDQKGYIAIEWWPDDYAAVRYATAKGVLVVGAAGNGAESLDDAVYERRPDGFPSWWRNPFNPSNRSSGAVLVGAGAPPPGTHGRDHGPDRSRLAFSNYGARVDAQGWGRETTTTGGFWDRPGDLQGGADEIAWYTDTFSGTSSASPIVVGALASLQGMLKAAGQQPMTPDRARATLRATGSPQQDAPGRPASQRIGNRPDLKAAVTNLLPSAVGSGQAERYWDELLPYPPELPPRLRLFVAGQWRNLDNPSPETRQAVHAAFAGGRPDVRVWFSDDEVVGLVVTG
>NZ_CP029192.1|WP_150219592.1|7175093_7176092_-|PAC2-family-protein
MIELEGVPELVDPVMVAAFEGWNDAGDAASAAVAHLDKEWKGEVFAALDAEDYYDFQVNRPTVWLDGGVRKITWPTTRLSVVRVGGDKPRDLVLVRGIEPSMRWRSFCNEILGFAHELGVELVVIMGALLGDTPHTRPVPVSGVTSDPDLARTMDLEETKYEGPTGIVGILQEACTHAGVPAVSLWAAVPHYVSQPPNPKATLALLNRLEDLIDLRIPLGELAEDARAWQVGVDQLAAEDSEVAEYVQSLEEARDTAELPEASGEAIAREFERYLRRRDGGEGGAGGAAYLRDSPSDRTRPPKPKPTQRPGQGTEDGEGESGDSGPPDSSDD
>NZ_CP029192.1|WP_150219593.1|7176243_7176915_-|FCD-domain-containing-protein
MAVTDEAIEKIKGMIVSGALRPGDRLPKESELAAELGLSRNSLREAVRALALIRILDVRQGDGTYVTSLDPQLLLEALSFVVDFHRDDTVLEFLAVRRILEPAATAMACAHISDAELDALSEQLDALGAAPSVEELVAADLEFHRGIVQTSGNSVLCSLLDGLSGPTTRARVWRGLTQEDAVSRTLHEHRAILTALRDRDAEAARSWATVHIASVEQWLRTTL
>NZ_CP029192.1|WP_150219594.1|7177098_7177653_+|MarR-family-transcriptional-regulator
MAGKKAAHQPDAVASIIADWARERPDLDTSPLEVLARLHRTFIRYNTRLTSAIEQHGLAVAGFDVLTALRRAGAPYRLTAGQLADSGLVSSAGVTLRIDRLEKDGLIVRERDADDRRVVYSRLTDAGLAKIDEVFAEHLENERRMLDGLSPAERRQLARLMSKLERSITEAGPREAQEDQAGEA
>NZ_CP029192.1|WP_150219595.1|7177634_7178648_-|Rieske-2Fe-2S-domain-containing-protein
MTLPVHDTADHIYATGLRNQWHPVVPSSFVTPGAMRKVTALGEQWLLFRRSDGTLSMLADRCPHRGAPLSLGKHLGDRVACWYHGVEVETDGTVSSVPGLPGCNLEGKKLVTSLPVREVGGAVLAYFGDERHPEPAELTLPEPLTDPEVDAILCYAEWNGPWRFAVENLLDPMHGAFLHHESHTMYNGDTTAKFRIRETDRGYFFEKTDQRGVNFDWVELCRTGVDWVDLTIPYPPSAGPGGPFGIVGMVCPVDEDRTGVFFWRYRRVRGWQRDTWRFLYKTLIEERHWQVLEQDRVMLEAMPADADQRENLYQHDLGVVRLRRMYRAEAVAQASPA
>NZ_CP029192.1|WP_150219596.1|7178649_7178874_-|hypothetical-protein
MTTTWPYLDVHQSRTHEPTPYEYKLAATLEEVFTKEGHELADVVRGLNARQVHAPDGAPWTEESFRAEMNRLGA
>NZ_CP029192.1|WP_150219597.1|7178920_7179871_-|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein
MTTSENRLDLRVRRMTWEAQGVLSVELAHPDGKPLPAWEPGAHVDVLVGGQVRQYSLCGDPRDTASYRIGVLNEPSSRGGSRYVHTQLRPGQTVTVTEPRNHFALEEAPAYVFVAGGIGITPILAMAREAARREAPWRLVYGGRTRDSMAFTDELDALGGALTLVPQDERGHIDLAEALEGQTLPEGTLVYCCGPEPLLAAVEAACPAERLRVERFAAPVVERSGGDAAFEVECRRSGVTLSVGPDTSVLAAAEAAGLPVRSSCRDGICGSCETRVLDGTPDHRDFLLSEAEHATNASMMICVSRCASGRRLVLDL
>NZ_CP029192.1|WP_150219598.1|7179884_7181516_-|thiamine-pyrophosphate-binding-protein
MRYDNGGDLLVAVLRELGIDTVFGIVSVHNLPLVEAVDRELRFVPVRHEATAVNAADAHGRARGSLGCALTSTGTGAGNAAGSLVEALSAGTSVLHVTGQVESRYLGSGRGFIHETKDQLGMLTAVSAYAATVPSAVDAGRVLREAARAALAAPGGPASVEWPVDLQYAAQTDTALDVPAPLFSEPLGAELAAAGELLASARRPLVWAGGGATRAGTELAELLTATGAGLLTSNSGRGTVPEDDPRVVGNFATTPEGRALLADADVVLSVGTHFRSNETADYSLELPAAHIQVDIDPAALGRVYPAAHTLCGDAAGVLRALLPYARRVGTEPGWSGRVTGVRDEVRANLRDAIGPQAALCDAIRAALPREAVVARDVTIASSSWGNRLLDMYDPRDNVFPRGGGIGQGLGMGIGAALARPGAPTVVLAGDGGLAVHLGELLTLAQEAPDLTLIVFNDGGYGVLRNMQDRYAERRSGVDLTTPDFALLARACGLPYRRIAAAEQAGPVVGEAVASGGPVLVEVDLAALGPMKSPFTPPVKIPAA
>NZ_CP029192.1|WP_150219599.1|7181525_7182299_-|SDR-family-oxidoreductase
MDLGLADRTYLVTGGSSGVGLATVRALLDEGANVATCGRDADRLKSIGTHERLFTAPCDVRDAAAVREFTGAAAHAFGGVDGLVNNAGQSRMKRFDETTEDDWRDELELKFAGVLNPLHAARPHLRASTAASVVNVNAVLAKQPEPRLITTSAARAGILNLSASLARELAPDAIRVNSVCLGLVDTGQWTRRHAAAGSGLPYEEWQAELAADRGVALGRLGRAEEVAYAILALLSPRASYITGTSIDVCGGVGRGIL

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_CP029192_2	2.1\|3947202\|52\|NZ_CP029192\|CRISPRCasFinder	3947202-3947253	52	NZ_CP029192.1	3451551-3451602	1	0.981
NZ_CP029192_11	11.1\|5321517\|53\|NZ_CP029192\|CRISPRCasFinder	5321517-5321569	53	NZ_CP029192.1	5321478-5321530	1	0.981
NZ_CP029192_2	2.1\|3947202\|52\|NZ_CP029192\|CRISPRCasFinder	3947202-3947253	52	NZ_CP029192.1	4249887-4249938	2	0.962
NZ_CP029192_16	16.1\|6954385\|21\|NZ_CP029192\|CRT	6954385-6954405	21	NZ_CP029192.1	598425-598445	2	0.905
NZ_CP029192_16	16.1\|6954385\|21\|NZ_CP029192\|CRT	6954385-6954405	21	NZ_CP029192.1	7059148-7059168	2	0.905

1. spacer 2.1|3947202|52|NZ_CP029192|CRISPRCasFinder matches to position: 3451551-3451602, mismatch: 1, identity: 0.981

cccgccgctccgcggcggatcactcccacccacccgcccgttcaccccgcac	CRISPR spacer
cccgccgctccgcggcggatcactcccacccacccacccgttcaccccgcac	Protospacer
***********************************.****************

2. spacer 11.1|5321517|53|NZ_CP029192|CRISPRCasFinder matches to position: 5321478-5321530, mismatch: 1, identity: 0.981

ggcggcgaaggctccccaggggcgccgagaactggctccggcggcgaaggctc	CRISPR spacer
ggtggcgaaggctccccaggggcgccgagaactggctccggcggcgaaggctc	Protospacer
**.**************************************************

3. spacer 2.1|3947202|52|NZ_CP029192|CRISPRCasFinder matches to position: 4249887-4249938, mismatch: 2, identity: 0.962

cccgccgctccgcggcggatcactcccacccacccgcccgttcaccccgcac	CRISPR spacer
cccgccgctccgcggcggatcgctcccacccacccgcccgtttaccccgcac	Protospacer
*********************.********************.*********

4. spacer 16.1|6954385|21|NZ_CP029192|CRT matches to position: 598425-598445, mismatch: 2, identity: 0.905

tcgcgacgaccgcgggcgcgg	CRISPR spacer
tcccgacgcccgcgggcgcgg	Protospacer
** ***** ************

5. spacer 16.1|6954385|21|NZ_CP029192|CRT matches to position: 7059148-7059168, mismatch: 2, identity: 0.905

tcgcgacgaccgcgggcgcgg	CRISPR spacer
tcgcgacgaacgcggccgcgg	Protospacer
********* ***** *****

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP029192_16	16.1\|6954385\|21\|NZ_CP029192\|CRT	6954385-6954405	21	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	1090960-1090980	1	0.952
NZ_CP029192_16	16.1\|6954385\|21\|NZ_CP029192\|CRT	6954385-6954405	21	NZ_CP013345	Sphingopyxis macrogoltabida strain 203N plasmid unnamed1, complete sequence	127914-127934	1	0.952
NZ_CP029192_1	1.3\|2683711\|22\|NZ_CP029192\|CRT	2683711-2683732	22	MH744425	Mycobacterium phage Wamburgrxpress, complete genome	65127-65148	2	0.909
NZ_CP029192_1	1.3\|2683711\|22\|NZ_CP029192\|CRT	2683711-2683732	22	MK494092	Mycobacterium phage Silverleaf, complete genome	64055-64076	2	0.909
NZ_CP029192_1	1.3\|2683711\|22\|NZ_CP029192\|CRT	2683711-2683732	22	NC_042313	Mycobacterium virus JoeDirt, complete genome	65735-65756	2	0.909
NZ_CP029192_1	1.3\|2683711\|22\|NZ_CP029192\|CRT	2683711-2683732	22	NZ_CP024895	Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence	145482-145503	2	0.909
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP021357	Rhodococcus sp. S2-17 plasmid pRB11, complete sequence	15124-15147	3	0.875
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP027299	Streptomyces sp. SGAir0924 plasmid unnamed_5	358836-358859	3	0.875
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP011667	Streptomyces sp. Mg1 plasmid pSMg1-3, complete sequence	68992-69015	3	0.875
NZ_CP029192_16	16.3\|6954472\|24\|NZ_CP029192\|CRT	6954472-6954495	24	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	196064-196087	3	0.875
NZ_CP029192_16	16.3\|6954472\|24\|NZ_CP029192\|CRT	6954472-6954495	24	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1617061-1617084	3	0.875
NZ_CP029192_16	16.3\|6954472\|24\|NZ_CP029192\|CRT	6954472-6954495	24	NC_009236	Burkholderia phage phiE12-2 chromosome, complete genome	6376-6399	3	0.875
NZ_CP029192_16	16.3\|6954472\|24\|NZ_CP029192\|CRT	6954472-6954495	24	CP000624	Burkholderia phage phiE12-2, complete genome	6376-6399	3	0.875
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	735135-735165	4	0.871
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP034352	Streptomyces sp. W1SF4 plasmid p2, complete sequence	227193-227223	4	0.871
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP048789	Roseobacter ponti strain DSM 106830 plasmid p1, complete sequence	3559-3582	4	0.833
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	872319-872342	4	0.833
NZ_CP029192_16	16.3\|6954472\|24\|NZ_CP029192\|CRT	6954472-6954495	24	NZ_CP029235	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436e, complete sequence	62032-62055	4	0.833
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	68399-68432	5	0.853
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	287592-287625	5	0.853
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1453425-1453452	5	0.821
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_022061	Mycobacterium phage KayaCho, complete genome	29938-29968	5	0.839
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	KJ433975	Mycobacterium phage 40BC, complete genome	29944-29974	5	0.839
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	KJ433973	Mycobacterium phage 39HC, complete genome	29944-29974	5	0.839
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_024145	Mycobacterium phage Hosp, complete genome	28140-28170	5	0.839
NZ_CP029192_16	16.2\|6954427\|24\|NZ_CP029192\|CRT	6954427-6954450	24	NZ_CP040452	Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence	596754-596777	5	0.792
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4864921-4864960	6	0.85
NZ_CP029192_1	1.2\|2683648\|34\|NZ_CP029192\|CRT	2683648-2683681	34	MH271302	Gordonia phage Margaret, complete genome	27623-27656	6	0.824
NZ_CP029192_3	3.2\|4182784\|30\|NZ_CP029192\|CRISPRCasFinder	4182784-4182813	30	NZ_KJ599675	Micrococcus sp. A7 plasmid pLMA7, complete sequence	33408-33437	6	0.8
NZ_CP029192_3	3.2\|4182784\|30\|NZ_CP029192\|CRISPRCasFinder	4182784-4182813	30	NC_024972	Micrococcus sp. A1 plasmid pLMA1, complete sequence	46763-46792	6	0.8
NZ_CP029192_3	3.2\|4182784\|30\|NZ_CP029192\|CRISPRCasFinder	4182784-4182813	30	NZ_CP025617	Micrococcus luteus strain SGAir0127 plasmid pSGAir0127	47875-47904	6	0.8
NZ_CP029192_3	3.2\|4182784\|30\|NZ_CP029192\|CRISPRCasFinder	4182784-4182813	30	NC_019941	Thioflavicoccus mobilis 8321 plasmid pTHIMO01, complete sequence	51411-51440	6	0.8
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	MH825699	Streptomyces phage Darolandstone, complete genome	4068-4098	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	613440-613470	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1129880-1129910	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1576399-1576429	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1501034-1501064	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	397898-397928	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1583850-1583880	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	1293498-1293528	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	1541762-1541792	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1595330-1595360	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1593731-1593761	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1593731-1593761	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1593731-1593761	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1593731-1593761	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1593731-1593761	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	457434-457464	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1501440-1501470	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1482090-1482120	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1535037-1535067	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1574236-1574266	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1591046-1591076	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1593734-1593764	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	451489-451519	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	451489-451519	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP013553	Rhizobium phaseoli strain N931 plasmid pRphaN931a, complete sequence	66706-66736	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP013559	Rhizobium phaseoli strain N841 plasmid pRphaN841b, complete sequence	66746-66776	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	434624-434654	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP013564	Rhizobium phaseoli strain N831 plasmid pRphaN831a, complete sequence	66706-66736	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	796515-796545	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	796515-796545	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	796516-796546	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	796512-796542	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	796518-796548	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP012383	Streptomyces ambofaciens ATCC 23877 plasmid pSAM1, complete sequence	62237-62267	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	CP054924	Verrucosispora sp. NA02020 plasmid unnamed, complete sequence	17329-17359	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_015409	Verrucosispora maris AB-18-032 plasmid pVMKU, complete sequence	45352-45382	6	0.806
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP038146	Streptomyces sp. S501 plasmid unnamed, complete sequence	19705-19735	6	0.806
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NZ_CP047145	Streptomyces sp. HF10 plasmid plas1, complete sequence	35075-35114	7	0.825
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NZ_CP046906	Streptomyces sp. QHH-9511 plasmid unnamed, complete sequence	14781-14814	7	0.794
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	122224-122257	7	0.794
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP025016	Rhizobium leguminosarum strain Norway plasmid pRLN4, complete sequence	76549-76576	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP025506	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvE, complete sequence	18406-18433	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP030763	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed3, complete sequence	458314-458341	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NC_012848	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence	252718-252745	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP022668	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR3, complete sequence	471154-471181	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP050088	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b6, complete sequence	96182-96209	7	0.75
NZ_CP029192_8	8.1\|5292020\|28\|NZ_CP029192\|CRISPRCasFinder	5292020-5292047	28	NZ_CP050092	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence	288108-288135	7	0.75
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP031166	Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence	542414-542444	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	114588-114618	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	2734692-2734722	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP051544	Paracoccus sanguinis strain OM2164 plasmid pPspOM44, complete sequence	8662-8692	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	245036-245066	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_010905	Amycolatopsis benzoatilytica strain DSM 43387 plasmid pA387, complete sequence	11163-11193	7	0.774
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	382889-382919	7	0.774
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NZ_CP048642	Streptomyces aureoverticillatus strain HN6 plasmid unnamed, complete sequence	18940-18979	8	0.8
NZ_CP029192_1	1.2\|2683648\|34\|NZ_CP029192\|CRT	2683648-2683681	34	MT657344	Microbacterium phage Kauala, complete genome	28759-28792	8	0.765
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NC_004320	Corynebacterium efficiens YS-314 plasmid pCE3, complete sequence	23489-23522	8	0.765
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1043602-1043632	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	769469-769499	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP036407	Komagataeibacter saccharivorans strain JH1 plasmid p92689, complete sequence	83962-83992	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP016457	Sphingobium sp. RAC03 plasmid pBSY17_2, complete sequence	1323-1353	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	345564-345594	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_LR134468	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence	60464-60494	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP022365	Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence	127843-127873	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP023993	Streptomyces malaysiensis strain DSM 4137 plasmid unnamed, complete sequence	48622-48652	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	293932-293962	8	0.742
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP011869	Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence	64938-64968	8	0.742
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	869474-869513	9	0.775
NZ_CP029192_1	1.2\|2683648\|34\|NZ_CP029192\|CRT	2683648-2683681	34	NZ_CP047145	Streptomyces sp. HF10 plasmid plas1, complete sequence	35084-35117	9	0.735
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	780360-780393	9	0.735
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	MG298964	Streptomyces phage Alsaber, complete genome	23953-23986	9	0.735
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	MT711978	Streptomyces phage Endor1, complete genome	24383-24416	9	0.735
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	MK967385	Gordonia phage SheckWes, complete genome	27206-27239	9	0.735
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	429959-429989	9	0.71
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP032350	Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence	164565-164595	9	0.71
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NC_018836	Streptomyces phage phiHau3, complete genome	31371-31401	9	0.71
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP019671	Burkholderia cenocepacia strain VC12308 plasmid unnamed, complete sequence	1960-1990	10	0.677
NZ_CP029192_9	9.2\|5292419\|31\|NZ_CP029192\|CRISPRCasFinder	5292419-5292449	31	NZ_CP026703	Serratia marcescens strain AR_0027 plasmid unitig_1_pilon, complete sequence	20133-20163	10	0.677
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	MG099941	Gordonia phage Bjanes7, complete genome	26053-26092	11	0.725
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NC_041883	Gordonia phage Attis, complete genome	26053-26092	11	0.725
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	MK801734	Gordonia phage LordFarquaad, complete genome	26053-26092	11	0.725
NZ_CP029192_1	1.1\|2683579\|40\|NZ_CP029192\|CRT	2683579-2683618	40	NC_031251	Gordonia phage SoilAssassin, complete genome	26052-26091	11	0.725
NZ_CP029192_1	1.4\|2683762\|34\|NZ_CP029192\|CRT	2683762-2683795	34	KJ194582	Mycobacterium phage Hawkeye, complete genome	7585-7618	11	0.676

1. spacer 16.1|6954385|21|NZ_CP029192|CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 1, identity: 0.952

tcgcgacgaccgcgggcgcgg	CRISPR spacer
tcgcgacgaccgcgggcgcga	Protospacer
********************.

2. spacer 16.1|6954385|21|NZ_CP029192|CRT matches to NZ_CP013345 (Sphingopyxis macrogoltabida strain 203N plasmid unnamed1, complete sequence) position: , mismatch: 1, identity: 0.952

tcgcgacgaccgcgggcgcgg	CRISPR spacer
tcgcgacgaccgcgggcgcgc	Protospacer
********************

3. spacer 1.3|2683711|22|NZ_CP029192|CRT matches to MH744425 (Mycobacterium phage Wamburgrxpress, complete genome) position: , mismatch: 2, identity: 0.909

ctgccttcttcgccgtcgccgt	CRISPR spacer
atgccttcttcgccgtcgtcgt	Protospacer
 *****************.***

4. spacer 1.3|2683711|22|NZ_CP029192|CRT matches to MK494092 (Mycobacterium phage Silverleaf, complete genome) position: , mismatch: 2, identity: 0.909

ctgccttcttcgccgtcgccgt	CRISPR spacer
atgccttcttcgccgtcgtcgt	Protospacer
 *****************.***

5. spacer 1.3|2683711|22|NZ_CP029192|CRT matches to NC_042313 (Mycobacterium virus JoeDirt, complete genome) position: , mismatch: 2, identity: 0.909

ctgccttcttcgccgtcgccgt	CRISPR spacer
atgccttcttcgccgtcgtcgt	Protospacer
 *****************.***

6. spacer 1.3|2683711|22|NZ_CP029192|CRT matches to NZ_CP024895 (Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence) position: , mismatch: 2, identity: 0.909

ctgccttcttcgccgtcgccgt	CRISPR spacer
cagccttcttcgccgtcgccgc	Protospacer
* *******************.

7. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP021357 (Rhodococcus sp. S2-17 plasmid pRB11, complete sequence) position: , mismatch: 3, identity: 0.875

cgggcggcccggtggtggcgggtt	CRISPR spacer
ggtgcgggccggtggtggcgggtt	Protospacer
 * **** ****************

8. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP027299 (Streptomyces sp. SGAir0924 plasmid unnamed_5) position: , mismatch: 3, identity: 0.875

cgggcggcccggtggtggcgggtt	CRISPR spacer
cgggcggcgcgggggtggcgggtg	Protospacer
******** *** **********

9. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP011667 (Streptomyces sp. Mg1 plasmid pSMg1-3, complete sequence) position: , mismatch: 3, identity: 0.875

cgggcggcccggtggtggcgggtt	CRISPR spacer
cgggcggcccggtagtggctggtg	Protospacer
*************.***** ***

10. spacer 16.3|6954472|24|NZ_CP029192|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 3, identity: 0.875

tgacggcgaccgcggtggataccg	CRISPR spacer
ggacggccaccgcggtggagaccg	Protospacer
 ****** *********** ****

11. spacer 16.3|6954472|24|NZ_CP029192|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 3, identity: 0.875

tgacggcgaccgcggtggataccg	CRISPR spacer
ggacggccaccgcggtggagaccg	Protospacer
 ****** *********** ****

12. spacer 16.3|6954472|24|NZ_CP029192|CRT matches to NC_009236 (Burkholderia phage phiE12-2 chromosome, complete genome) position: , mismatch: 3, identity: 0.875

tgacggcgaccgcggtggataccg	CRISPR spacer
cgccggcggccgcggtggataccg	Protospacer
.* *****.***************

13. spacer 16.3|6954472|24|NZ_CP029192|CRT matches to CP000624 (Burkholderia phage phiE12-2, complete genome) position: , mismatch: 3, identity: 0.875

tgacggcgaccgcggtggataccg	CRISPR spacer
cgccggcggccgcggtggataccg	Protospacer
.* *****.***************

14. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 4, identity: 0.871

cgcac-cccagccgcccggcccgcccggcgca	CRISPR spacer
-gaacgccctgccgcccggcccgcccggccca	Protospacer
 * ** *** ******************* **

15. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP034352 (Streptomyces sp. W1SF4 plasmid p2, complete sequence) position: , mismatch: 4, identity: 0.871

cgcaccccagccgcccggcccgcccggcgca-	CRISPR spacer
cgcaccccggccgcccggcgcgccc-gcgcgg	Protospacer
********.********** ***** ****.

16. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP048789 (Roseobacter ponti strain DSM 106830 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.833

cgggcggcccggtggtggcgggtt	CRISPR spacer
cgggctgcccggtggtggcggcac	Protospacer
***** ***************  .

17. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 4, identity: 0.833

cgggcggcccggtggtggcgggtt	CRISPR spacer
cgggcggcccggtcgtggcggtgg	Protospacer
************* *******

18. spacer 16.3|6954472|24|NZ_CP029192|CRT matches to NZ_CP029235 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436e, complete sequence) position: , mismatch: 4, identity: 0.833

tgacggcgaccgcggtggataccg	CRISPR spacer
gtccggcgaccgcggtggaaaccg	Protospacer
   **************** ****

19. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 5, identity: 0.853

tggccgtg--gtcttcttcgccgtggccttcgtggc	CRISPR spacer
--tccgtgacgccttcttcgccgtggccttcttggc	Protospacer
   *****  *.******************* ****

20. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 5, identity: 0.853

tggccgtg--gtcttcttcgccgtggccttcgtggc	CRISPR spacer
--tccgtgacgccttcttcgccgtggccttcttggc	Protospacer
   *****  *.******************* ****

21. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 5, identity: 0.821

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgccgcggacgcctccgcgtatgtctac	Protospacer
***.*****************.*  **.

22. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_022061 (Mycobacterium phage KayaCho, complete genome) position: , mismatch: 5, identity: 0.839

cgcaccccagccgcccggc---ccgcccggcgca	CRISPR spacer
cgcacccgagccgcccggcgcgctgcccggc---	Protospacer
******* ***********   *.*******

23. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to KJ433975 (Mycobacterium phage 40BC, complete genome) position: , mismatch: 5, identity: 0.839

cgcaccccagccgcccggc---ccgcccggcgca	CRISPR spacer
cgcacccgagccgcccggcgcgctgcccggc---	Protospacer
******* ***********   *.*******

24. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to KJ433973 (Mycobacterium phage 39HC, complete genome) position: , mismatch: 5, identity: 0.839

cgcaccccagccgcccggc---ccgcccggcgca	CRISPR spacer
cgcacccgagccgcccggcgcgctgcccggc---	Protospacer
******* ***********   *.*******

25. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_024145 (Mycobacterium phage Hosp, complete genome) position: , mismatch: 5, identity: 0.839

cgcaccccagccgcccggc---ccgcccggcgca	CRISPR spacer
cgcacccgagccgcccggcgcgctgcccggc---	Protospacer
******* ***********   *.*******

26. spacer 16.2|6954427|24|NZ_CP029192|CRT matches to NZ_CP040452 (Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence) position: , mismatch: 5, identity: 0.792

cgggcggcccggtggtggcgggtt	CRISPR spacer
accacggcccggtggtggcgggta	Protospacer
   .*******************

27. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 6, identity: 0.85

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
cggcggtcttcttggccggggccttcttcgcggccgcctt	Protospacer
 ***************** ************ ****   *

28. spacer 1.2|2683648|34|NZ_CP029192|CRT matches to MH271302 (Gordonia phage Margaret, complete genome) position: , mismatch: 6, identity: 0.824

ccggggtcgccttcttggccgtggccttggtggc	CRISPR spacer
tcgccggcgccttcttggccggggccttggcggc	Protospacer
.**  * ************** ********.***

29. spacer 3.2|4182784|30|NZ_CP029192|CRISPRCasFinder matches to NZ_KJ599675 (Micrococcus sp. A7 plasmid pLMA7, complete sequence) position: , mismatch: 6, identity: 0.8

aacctcgccccgtccggggaccacgatcca	CRISPR spacer
gacctcgccccggccggggaacacgaggcc	Protospacer
.*********** ******* *****  *

30. spacer 3.2|4182784|30|NZ_CP029192|CRISPRCasFinder matches to NC_024972 (Micrococcus sp. A1 plasmid pLMA1, complete sequence) position: , mismatch: 6, identity: 0.8

aacctcgccccgtccggggaccacgatcca	CRISPR spacer
gacctcgccccggccggggagcacgaggcc	Protospacer
.*********** ******* *****  *

31. spacer 3.2|4182784|30|NZ_CP029192|CRISPRCasFinder matches to NZ_CP025617 (Micrococcus luteus strain SGAir0127 plasmid pSGAir0127) position: , mismatch: 6, identity: 0.8

aacctcgccccgtccggggaccacgatcca	CRISPR spacer
gacctcgccccggccggggagcacgaggcc	Protospacer
.*********** ******* *****  *

32. spacer 3.2|4182784|30|NZ_CP029192|CRISPRCasFinder matches to NC_019941 (Thioflavicoccus mobilis 8321 plasmid pTHIMO01, complete sequence) position: , mismatch: 6, identity: 0.8

aacctcgccccgtccggggacca-cgatcca	CRISPR spacer
cacctccccgcgtccggggaccaccgaagc-	Protospacer
 ***** ** ************* ***  *

33. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to MH825699 (Streptomyces phage Darolandstone, complete genome) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cgcacccaagccgcccggcccgcccacgccc	Protospacer
******* *****************.   *

34. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cggcggcccgccgcccggccctcccggcgca	Protospacer
**    ** ************ *********

35. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

36. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

37. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

38. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

39. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

40. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

41. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

42. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

43. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

44. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

45. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

46. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

47. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

48. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

49. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

50. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

51. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

52. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

53. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

54. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

55. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

56. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

57. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP013553 (Rhizobium phaseoli strain N931 plasmid pRphaN931a, complete sequence) position: , mismatch: 6, identity: 0.806

cgcacc-ccagccgcccggcccgcccggcgca	CRISPR spacer
-acgccggcagccggctggcccgcccggcgca	Protospacer
 .*.**  ****** *.***************

58. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP013559 (Rhizobium phaseoli strain N841 plasmid pRphaN841b, complete sequence) position: , mismatch: 6, identity: 0.806

cgcacc-ccagccgcccggcccgcccggcgca	CRISPR spacer
-acgccggcagccggctggcccgcccggcgca	Protospacer
 .*.**  ****** *.***************

59. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

60. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP013564 (Rhizobium phaseoli strain N831 plasmid pRphaN831a, complete sequence) position: , mismatch: 6, identity: 0.806

cgcacc-ccagccgcccggcccgcccggcgca	CRISPR spacer
-acgccggcagccggctggcccgcccggcgca	Protospacer
 .*.**  ****** *.***************

61. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

62. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

63. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

64. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

65. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

66. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

67. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

68. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

69. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

70. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

71. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccggcgca----	CRISPR spacer
cgcagcccagccgcccggccagc----cgcaccac	Protospacer
**** *************** **    ****

72. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP012383 (Streptomyces ambofaciens ATCC 23877 plasmid pSAM1, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcccgg-cgca	CRISPR spacer
ccacccccaacctcccggcccgcccggtcgc-	Protospacer
*   *****.** ************** ***

73. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to CP054924 (Verrucosispora sp. NA02020 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

-cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ctgca-cccacccgcccggcccgaccggcacg	Protospacer
 .*** **** ************ *****.*.

74. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_015409 (Verrucosispora maris AB-18-032 plasmid pVMKU, complete sequence) position: , mismatch: 6, identity: 0.806

-cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ctgca-cccacccgcccggcccgaccggcacc	Protospacer
 .*** **** ************ *****.*

75. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP038146 (Streptomyces sp. S501 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

cgcaccccagccgcccggcccgcc-cggcgca	CRISPR spacer
cggaacccagccgcccggcccgctgctgccc-	Protospacer
** * ******************. * ** *

76. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NZ_CP047145 (Streptomyces sp. HF10 plasmid plas1, complete sequence) position: , mismatch: 7, identity: 0.825

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
cggccgtcttcttggccgtggccttcttcgcgggccgctt	Protospacer
 *** ************************** * * *  *

77. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NZ_CP046906 (Streptomyces sp. QHH-9511 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.794

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
tccgggcggtcttcttcgccgtggtcttcttggc	Protospacer
*    *.*****************.**** ****

78. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 7, identity: 0.794

---tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
atctggc---ggtcttctccgccgcggccttcgtgct	Protospacer
   ****   ********.*****.********** .

79. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP025016 (Rhizobium leguminosarum strain Norway plasmid pRLN4, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccaa	Protospacer
****** ************** .. .*

80. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP025506 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvE, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

81. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP030763 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

82. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NC_012848 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

83. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022668 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR3, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

84. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP050088 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b6, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

85. spacer 8.1|5292020|28|NZ_CP029192|CRISPRCasFinder matches to NZ_CP050092 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b6, complete sequence) position: , mismatch: 7, identity: 0.75

cgctgcggacgcctccgcgtacggatat	CRISPR spacer
cgctgccgacgcctccgcgtagaaccag	Protospacer
****** ************** .. .*

86. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP031166 (Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gacacaccagtcgcccggcccgcccgcgcca	Protospacer
 .*** ****.***************   **

87. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
accaccccggccgcccggcccggccgcggct	Protospacer
  ******.************* ***  **

88. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cgagcaccagtcgcccgtcccgcccggcgtt	Protospacer
** .* ****.****** ***********.

89. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP051544 (Paracoccus sanguinis strain OM2164 plasmid pPspOM44, complete sequence) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cccgccccatctgcccggcccgcccggcctg	Protospacer
* *.***** *.**************** ..

90. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 7, identity: 0.774

cgcacc-ccagccgcccggcccgcccggcgca	CRISPR spacer
-gcgtcaccagcgacccggcccgcccggcgtc	Protospacer
 **..* ***** .****************.

91. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_010905 (Amycolatopsis benzoatilytica strain DSM 43387 plasmid pA387, complete sequence) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
agcaccacggccgcccggcccgccgtgcccg	Protospacer
 ***** *.***************  ** *.

92. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.774

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ccgatcccagccgcacggcccgtccggcccg	Protospacer
*  *.********* *******.***** *.

93. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NZ_CP048642 (Streptomyces aureoverticillatus strain HN6 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.8

gggcggtcttcttggccgtggccttcttcgccgccggggt-	CRISPR spacer
ccgcggtcttcttggccgtggtcttcttcg-ggctggtctt	Protospacer
  *******************.********  **.**  *

94. spacer 1.2|2683648|34|NZ_CP029192|CRT matches to MT657344 (Microbacterium phage Kauala, complete genome) position: , mismatch: 8, identity: 0.765

ccggggtcgccttcttggccgtggccttggtggc	CRISPR spacer
tggccggtgccttcttcgccgtggccttgggggc	Protospacer
. *  * .******** ************* ***

95. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NC_004320 (Corynebacterium efficiens YS-314 plasmid pCE3, complete sequence) position: , mismatch: 8, identity: 0.765

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
tcgccgtggtctacgtcgccgtggccgcctcggt	Protospacer
* ********** * *********** .* .**.

96. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gggctcccagacgaccggcccgcccggctcc	Protospacer
 *  .***** ** ************** *

97. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gggctcccagacgaccggcccgcccggctcc	Protospacer
 *  .***** ** ************** *

98. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP036407 (Komagataeibacter saccharivorans strain JH1 plasmid p92689, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
tgcctgccagccgcccggcatgcccggcggc	Protospacer
.** . ************* .********

99. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP016457 (Sphingobium sp. RAC03 plasmid pBSY17_2, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ctcgacccagccgcccggcacgccctgcagg	Protospacer
* *. ************** ***** **. .

100. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cgaaccccagccgcccggtccgctcactgag	Protospacer
** ***************.****.*. .* .

101. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_LR134468 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cgacgtgcagccgcccggcccgcgcgacgcc	Protospacer
**   . **************** **.***

102. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP022365 (Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
tggcgcgcagcggcccggcctgcccggcgcg	Protospacer
.*   * **** ********.*********.

103. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP023993 (Streptomyces malaysiensis strain DSM 4137 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ggaagaccagcagcccggcccgcacggcgag	Protospacer
 * *  ***** *********** ***** .

104. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 8, identity: 0.742

-cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
tcacg-tccagccgccagggccgcccggcgat	Protospacer
 *.*. .********* ** **********

105. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP011869 (Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence) position: , mismatch: 8, identity: 0.742

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
cgtgtagcagtcgcccgccccgcccggcgcg	Protospacer
**...  ***.****** ************.

106. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.775

gggcggtcttcttggccgtggccttcttcgccg---ccggggt	CRISPR spacer
ccggggtcttcttggctgcggccttcttcgccgcgccctg---	Protospacer
  * ************.*.**************   ** *

107. spacer 1.2|2683648|34|NZ_CP029192|CRT matches to NZ_CP047145 (Streptomyces sp. HF10 plasmid plas1, complete sequence) position: , mismatch: 9, identity: 0.735

ccggggtcgccttcttggccgtggccttggtggc	CRISPR spacer
ttccggccgtcttcttggccgtggccttcttcgc	Protospacer
..  **.**.******************  * **

108. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.735

tggccgtggtcttcttcgccgtggccttcgtggc----	CRISPR spacer
ccgccgtggtcgtcttcggcgtggcc----gggcatct	Protospacer
. ********* ****** *******     ***

109. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to MG298964 (Streptomyces phage Alsaber, complete genome) position: , mismatch: 9, identity: 0.735

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
gcgtgctcgtcttcttcgccgtcgccttcttgac	Protospacer
  *.  * ************** ****** **.*

110. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to MT711978 (Streptomyces phage Endor1, complete genome) position: , mismatch: 9, identity: 0.735

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
gcgtgctcgtcttcttcgccgtggtcttcttgac	Protospacer
  *.  * ****************.**** **.*

111. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to MK967385 (Gordonia phage SheckWes, complete genome) position: , mismatch: 9, identity: 0.735

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
ccggtgcagccttcttcgccgcggccttcttggc	Protospacer
. * .*..*.***********.******* ****

112. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 9, identity: 0.71

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gttcggccagccgcccggcccgcacggcggg	Protospacer
  .   ***************** ***** .

113. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP032350 (Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.71

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
agcacccccgccgccccgcccgccccctctc	Protospacer
 ******* ******* ********  . .

114. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NC_018836 (Streptomyces phage phiHau3, complete genome) position: , mismatch: 9, identity: 0.71

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
ggtcggccagccgccaggcccgccgggcgtc	Protospacer
 *.   ********* ******** ****.

115. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP019671 (Burkholderia cenocepacia strain VC12308 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.677

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gatcgaccagccgcccggcccgccggtcggt	Protospacer
 ..   ****************** * **

116. spacer 9.2|5292419|31|NZ_CP029192|CRISPRCasFinder matches to NZ_CP026703 (Serratia marcescens strain AR_0027 plasmid unitig_1_pilon, complete sequence) position: , mismatch: 10, identity: 0.677

cgcaccccagccgcccggcccgcccggcgca	CRISPR spacer
gatcgaccagccgcccggcccgccggtcggt	Protospacer
 ..   ****************** * **

117. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to MG099941 (Gordonia phage Bjanes7, complete genome) position: , mismatch: 11, identity: 0.725

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
tcttcttcttcttggccggggcctttttcgccgctcgcgt	Protospacer
   .  ************ ******.********. * **

118. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NC_041883 (Gordonia phage Attis, complete genome) position: , mismatch: 11, identity: 0.725

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
tcttcttcttcttggccggggcctttttcgccgctcgcgt	Protospacer
   .  ************ ******.********. * **

119. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to MK801734 (Gordonia phage LordFarquaad, complete genome) position: , mismatch: 11, identity: 0.725

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
tcttcttcttcttggccggggcctttttcgccgctcgcgt	Protospacer
   .  ************ ******.********. * **

120. spacer 1.1|2683579|40|NZ_CP029192|CRT matches to NC_031251 (Gordonia phage SoilAssassin, complete genome) position: , mismatch: 11, identity: 0.725

gggcggtcttcttggccgtggccttcttcgccgccggggt	CRISPR spacer
tcttcttcttcttggccggggcctttttcgccgctcgcgt	Protospacer
   .  ************ ******.********. * **

121. spacer 1.4|2683762|34|NZ_CP029192|CRT matches to KJ194582 (Mycobacterium phage Hawkeye, complete genome) position: , mismatch: 11, identity: 0.676

tggccgtggtcttcttcgccgtggccttcgtggc	CRISPR spacer
ttgccgaggtcttcttcgccgtcgcccataccct	Protospacer
* **** *************** ***. ...  .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site	Prophage annotation

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_CP029192

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

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection