CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP036262	Planctomycetes bacterium FF011L chromosome, complete genome	22 crisprs	DinG,RT,cas3,WYL,DEDDh,csa3	3	8	1	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP036262_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_1

112732-112846

Orphan

Consensus_repeat	Method
TGCCGGGCGGCTCGCGCCGCACCGCTAGGATTTGCGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_1

>merge|NZ_CP036262|1|112732-112846|CRISPRCasFinder
TGCCGGGCGGCTCGCGCCGCACCGCTAGGATTTGCGCCCGCAAGCCGTCCGGCCGATGCGTTGGAAGCCGCACTTTCTTGCCGAGCGGCTCGCGCCGCACCGCTAGGATTTGCGC

>NZ_CP036262|1|1|112732-112846|CRISPRCasFinder
TGCCGGGCGGCTCGCGCCGCACCGCTAGGATTTGCGC	CCGCAAGCCGTCCGGCCGATGCGTTGGAAGCCGCACTTTCT
TGCCGAGCGGCTCGCGCCGCACCGCTAGGATTTGCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145349456.1\|120561_121371_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP036262.1\|WP_145354834.1\|117509_119540_-\|protein-kinase	unknown	unknown	gnl\|CDD\|214567
NZ_CP036262.1\|WP_145349455.1\|119668_120304_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349445.1\|101681_103064_+\|BBP7-family-outer-membrane-beta-barrel-protein	unknown	unknown	gnl\|CDD\|377874
NZ_CP036262.1\|WP_145349453.1\|116188_116707_+\|SET-domain-containing-protein-lysine-N-methyltransferase	unknown	unknown	gnl\|CDD\|380949
NZ_CP036262.1\|WP_145349444.1\|99381_101466_-\|preprotein-translocase-subunit-SecA	unknown	unknown	gnl\|CDD\|237253
NZ_CP036262.1\|WP_145349447.1\|109490_109838_+\|diacylglycerol-kinase-family-protein	unknown	unknown	gnl\|CDD\|260134
NZ_CP036262.1\|WP_145349449.1\|110649_112263_+\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145349441.1\|93481_93913_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|223725
NZ_CP036262.1\|WP_145349451.1\|114669_115740_+\|tetraacyldisaccharide-4'-kinase	unknown	unknown	gnl\|CDD\|376853
NZ_CP036262.1\|WP_145349440.1\|92571_93318_+\|MIP-family-channel-protein	unknown	unknown	gnl\|CDD\|223653
NZ_CP036262.1\|WP_145349458.1\|122727_123279_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|236608
NZ_CP036262.1\|WP_145349448.1\|110126_110348_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349442.1\|93976_94399_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370070
NZ_CP036262.1\|WP_145349452.1\|115863_116157_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|313734
NZ_CP036262.1\|WP_145349443.1\|94584_99258_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036262.1\|WP_145349446.1\|103467_109488_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380081
NZ_CP036262.1\|WP_145349457.1\|122487_122703_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235202
NZ_CP036262.1\|WP_145349450.1\|113013_114627_+\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145349454.1\|116826_117441_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145349456.1\|120561_121371_-\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	1.03281e-05
NZ_CP036262.1\|WP_145354834.1\|117509_119540_-\|protein-kinase	gnl\|CDD\|214567	smart00220, S_TKc, Serine/Threonine protein kinases, catalytic domain. Phosphotransferases. Serine or threonine-specific kinase subfamily.	1.54942e-68
NZ_CP036262.1\|WP_145349445.1\|101681_103064_+\|BBP7-family-outer-membrane-beta-barrel-protein	gnl\|CDD\|377874	pfam07585, BBP7, Putative beta barrel porin-7 (BBP7). This is a family of putative beta barrel porin-7 BBP7 proteins identified initially in Rhodopirellula baltica.	2.8056e-79
NZ_CP036262.1\|WP_145349453.1\|116188_116707_+\|SET-domain-containing-protein-lysine-N-methyltransferase	gnl\|CDD\|380949	cd19172, SET_SETD2, SET domain (including post-SET domain) found in SET domain-containing protein 2 (SETD2) and similar proteins. SETD2 (also termed HIF-1, huntingtin yeast partner B, huntingtin-interacting protein 1 (HIP-1), huntingtin-interacting protein B, lysine N-methyltransferase 3A or protein-lysine N-methyltransferase SETD2) acts as histone-lysine N-methyltransferase that specifically trimethylates 'Lys-36' of histone H3 (H3K36me3) using demethylated 'Lys-36' (H3K36me2) as substrate. It has been shown that methylation is a posttranslational modification of dynamic microtubules and that SETD2 methylates alpha-tubulin at lysine 40, the same lysine that is marked by acetylation on microtubules. Methylation of microtubules occurs during mitosis and cytokinesis and can be ablated by SETD2 deletion, which causes mitotic spindle and cytokinesis defects, micronuclei, and polyploidy.	3.73454e-25
NZ_CP036262.1\|WP_145349444.1\|99381_101466_-\|preprotein-translocase-subunit-SecA	gnl\|CDD\|237253	PRK12898, secA, preprotein translocase subunit SecA; Reviewed.	0
NZ_CP036262.1\|WP_145349447.1\|109490_109838_+\|diacylglycerol-kinase-family-protein	gnl\|CDD\|260134	cd14265, UDPK_IM_like, Integral membrane undecaprenol kinase and similar enzymes. This mostly bacterial family of homo-trimeric integral membrane enzymes, the products of the dgkA gene, catalyzes the ATP-dependent phosphorylation of undecaprenol to undecaprenyl phosphate. C55-isoprenyl (undecaprenyl) pyroposphate acts as a scaffold for the assembly of peptidoglycan components; undecaprenol kinase (UDPK) is involved in recycling undecaprenyl units for re-use in the peptidoglycan biosynthesis. UDPK does not participate in the de-novo biosynthesis of undecaprenyl phosphate. Gram-positive bacteria have a large pool of free undecaprenol, in contrast to gram-negative bacteria. UDPK may also play a role in a stress-induced pathway that affects the function of ribosomes. In Streptococcus mutans, UDPK has been shown to be required for biofilm formation, such as in the case of smooth surface dental caries. Members of the UDPK family have low activity as diacylglycerol kinases (DAGK), and many of them are annotated as DAGKs.	4.61901e-34
NZ_CP036262.1\|WP_145349449.1\|110649_112263_+\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	2.58962e-31
NZ_CP036262.1\|WP_145349441.1\|93481_93913_-\|peptidylprolyl-isomerase	gnl\|CDD\|223725	COG0652, PpiB, Peptidyl-prolyl cis-trans isomerase (rotamase) - cyclophilin family [Posttranslational modification, protein turnover, chaperones].	7.21926e-69
NZ_CP036262.1\|WP_145349451.1\|114669_115740_+\|tetraacyldisaccharide-4'-kinase	gnl\|CDD\|376853	pfam02606, LpxK, Tetraacyldisaccharide-1-P 4'-kinase. This family consists of tetraacyldisaccharide-1-P 4'-kinase also known as Lipid-A 4'-kinase or Lipid A biosynthesis protein LpxK, EC:2.7.1.130. This enzyme catalyzes the reaction: ATP + 2,3-bis(3-hydroxytetradecanoyl)-D -glucosaminyl-(beta-D-1,6)-2,3-bis(3-hydroxytetradecanoyl)-D-glu cosam inyl beta-phosphate <=> ADP + 2,3,2',3'-tetrakis(3-hydroxytetradecanoyl)-D- glucosaminyl-1,6-beta-D-glucosamine 1,4'-bisphosphate. This enzyme is involved in the synthesis of lipid A portion of the bacterial lipopolysaccharide layer (LPS). The family contains a P-loop motif at the N-terminus.	3.05159e-91
NZ_CP036262.1\|WP_145349440.1\|92571_93318_+\|MIP-family-channel-protein	gnl\|CDD\|223653	COG0580, GlpF, Glycerol uptake facilitator and related permeases (Major Intrinsic Protein Family) [Carbohydrate transport and metabolism].	1.12903e-71
NZ_CP036262.1\|WP_145349458.1\|122727_123279_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|236608	PRK09652, PRK09652, RNA polymerase sigma factor RpoE; Provisional.	1.51501e-44
NZ_CP036262.1\|WP_145349442.1\|93976_94399_-\|hypothetical-protein	gnl\|CDD\|370070	pfam08695, Coa1, Cytochrome oxidase complex assembly protein 1. Coa1 is an inner mitochondrial membrane protein that associates with Shy1 and is required for cytochrome oxidase complex IV assembly. It contains a conserved hydrophobic segment (amino acids 74-92) with the potential to form a membrane-spanning helix. The N-terminus of Coa1 is rich in positively charged amino acids and could form an amphipathic alpha helix, characteristic of a mitochondrial presequence. A cleavage site for the mitochondrial processing peptidase is predicted adjacent to the presequence. Upon in vitro import into mitochondria, Coa1 is processed to a mature form, indicating that it possesses a cleavable presequence. The eukaryotic cytochrome oxidase complex consists of 12-13 subunits, with three mitochondrial encoded subunits, Cox1-Cox3, forming the core enzyme. Translation of the Cox1 transcript requires the two promoters, Pet309 and Mss51, and the latter has an additional role in translational elongation. Coa1 is necessary for linking the activity of Mss51 to Cox1 insertion into the assembly complex.	1.15771e-05
NZ_CP036262.1\|WP_145349452.1\|115863_116157_+\|hypothetical-protein	gnl\|CDD\|313734	pfam10571, UPF0547, Uncharacterized protein family UPF0547. This domain contains a zinc-ribbon motif.	0.000340375
NZ_CP036262.1\|WP_145349443.1\|94584_99258_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	9.50541e-20
NZ_CP036262.1\|WP_145349446.1\|103467_109488_+\|hypothetical-protein	gnl\|CDD\|380081	pfam17973, bMG10, Bacterial Alpha-2-macroglobulin MG10 domain. Alpha-2-macroglobulins (A2Ms) are plasma proteins that trap and inhibit a broad range of proteases and are major components of the eukaryotic innate immune system. However, A2M-like proteins were identified in pathogenically invasive bacteria and species that colonize higher eukaryotes. Bacterial A2Ms are located in the periplasm where they are believed to provide protection to the cell by trapping external proteases through a covalent interaction with an activated thioester. This domain is found on the C-terminal region in A2Ms in bacteria. Structure analysis of Salmonella enterica ser A2Ms (SA-A2Ms) show that they are composed of 13 domains, all of which fold as variants of beta sandwiches with the exception of the TED, which consists of 14 alpha helices. Most of the beta sandwich domains appear to serve a structural role and are referred to as the macroglobulin-like (MG) domains. This is the MG10 domain. MG10 is markedly different from the other MG domains in that it has more beta strands and an alpha helix. The position of MG10 is stabilized by, in addition to other hydrogen bonds, the formation of a beta sheet with MG9.	1.82016e-32
NZ_CP036262.1\|WP_145349450.1\|113013_114627_+\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	1.50355e-43
NZ_CP036262.1\|WP_145349457.1\|122487_122703_-\|hypothetical-protein	gnl\|CDD\|235202	PRK04023, PRK04023, DNA polymerase II large subunit; Validated.	0.00843509

>NZ_CP036262.1|WP_145349449.1|110649_112263_+|DUF1559-domain-containing-protein
MSNVSFRPLLGAGLLVLFSLSLPAQEDVSNKLSAEFVPDNALAAIFASPSKVLQDPSFEMMPIEVLQAQGLEMIGVDPMHIDQLTVVVGPPGPQGPVGGVVIQFSQDYSIEDLNPQIFREAEPQESNGREVYLLAGPPNTVLFRKDARTFIIGVGNYLNSIVDGNQGQGSLARLLPRIPDQNGITAVAVLDQIRPMLTGLLKQNVRQMPAQVQGVVRLPELTDALVVNVKPAGLLNFQATVVALCTDADAAQEAAGVLNDSIDFGIAKVVEDATQGMDSSDPVRNASAKYGVRLADFLGNSFRPKIVGNRLVIKPASNAGTVGALVGLLLPAIQAARGAASRVRSSNNQRQILLAMHIYHDTYQKLPDAQIKDKEGKPLLSWRVSILPFIEHQALYEQFHLDEPWDSEHNLPLANQMPDAFRHPDLPTEKNETVYQVAAGKGLMFDNDKANRFRDVGDGLSNTVLLTETDAAHAVVWSKPEDSSIDMNDPAGHLHVAPGDVYQFGFGDGSVQAIPLDMDLETLKALFTRAGGEFVKR
>NZ_CP036262.1|WP_145349448.1|110126_110348_-|hypothetical-protein
MRQSKVSNTKRKQPGGRQILAGGESRRSNKDGYQSPAGDRVYPSPILSPAGLDNALEAIRRLTPPASICRPLG
>NZ_CP036262.1|WP_145349447.1|109490_109838_+|diacylglycerol-kinase-family-protein
MSKFRNAFQGLVFAMRGQSSFVIHLVMAAAVIGLAAICQVESWRWAVLLLAIGMVLALETINSAIECLVHRLHPEHDPEIGKVLDMAAGAVLLGAIFAAAVGLIVLLPPLLEWFG
>NZ_CP036262.1|WP_145349446.1|103467_109488_+|hypothetical-protein
MAASRRFPRLFLALGVFVCVTPFLLGAQSQEDRWKKVDKAIAEGLPKTAISELQPIIDSALAGEKYDEAIKAIGLRVSLEANIQGNQPAERIVRLEAEVEKAAEPMKPVMRAILANAYWQYFQQNQWRFQQRTQTSGPPGDDFTTWSLPQILAHVDAQFQAVLADAETLQEIPVRDFEAVLDKGNAPDSYRPTMYDVLAHNALDFYASGVQAGSQVQDSFVLTIDSPVFADSQTFMDWKPETSDSDSRLVKAITIYQDLLRFHASDDDPDARLDVDLLRLEFGNNEAAGETKPKSERFIAALRRFIDQNEDHPIVARALHLWALDLHSQGDLVKAHAIATRGLEQFPGTVGGNRCFNLIQSIEAKSASALTERVWNEPAPTIDIQYRNVNKVYLRLVPFDFKKMVIDSQRWQATAINEQTLQELLATKPTKAWAVDLPATTDYQLREESIPAPLDVPLGSYFLLASENADFSSRDNQISVAEVWRSDLAIVSRSRNGEGIVEGLVLDASSGNPIQGASVQAWNRGNRNETQPLKVVRTDRDGRYRLQDADRLQLQILVTDGKQQLSTDNMVRAYRNNQNSRLQEQTRFFTDRAIYRPGQTIRYKGVCLEFEQEKDLYQTIPHRDVVVVLRDVNGEEVERLKHRTNGNGSFQGSFTAPRGRVTGMMTLMVDGKPSGATSIRVEEYKRPKFRVAIDPPTKPAQLGEDVQVSGKATAYTGASIGGAKVQYRVVREVRYPDWWYWRCWWMPPANSGPQEIVNGVTTTEADGGFDVLFTARPDESVLRESEPVFQFTIYADVTDLTGETRSSSQTVRVGYTTLAATLNAAAWQTADKPVSIDVQTSTLNGDGRPAKGTLKVYALQQPEEVMRAELSGGRGRIPYRGNAMPASPDPANPNSWDLGKMVADLSVETDAGGKATVEVPLPAGIYRAVYETTDSAGEKVTALLQRNVLDLEAEDLAIRIPDLFAIKESTLEPGDDLVAVWGSGYEQARAFVEIEHRGKILQEYWTNPQQTQFVIEQSVTEAMRGGFTLRVTMVRENRAYLHTEQIQVPWTNKELDIQWERFVSKLAPGAVEKWTAKIQGPDAEVMAAEMVATLYDASLDAFAPHSWMSGFNVFRTDHSSLYSQFENNAESLRTLVSNRRTDQRDGSLSYRHLANSLISQAYGFGFMNRNRMMRRGGAPEMMMDSAPMGMGGMGGSAMMQKGAAMSASELAPAAAPMPADADAAIAGGGEEAAKSEPDLTNVTARKNLAETAFFFPQLIANDDGTVTMEFTMPEALTEWKFIGFAHDNQLRAGILDGTAVTSKDLMVEPNPPRFVREGDRLEFTVKVSNQSPTRQTGKVRLAFQDARSGDSVDASLGNANGDKEFAIAAGESQTFAWQIEVPDNQGVLVYKAVGATGRLSDGEEGFLPVLSRKVLVTESLPLPIRGNQTKKFVFDRLLHSGDSDSLQNQSLTVQMVSNPAWYAVMALPYLMEYPHQCSEQTFNRLYANALGQSIANSDPRIEQVFEQWRGTEALDSPLEKNEDLKSVMLEETPWLRDGKNESQARRNVGILFDGNRLSDEINRNEQQLAEMQLENGMWPWFPGGGENEYITLYITTGFGRLRHLGVDIDVAPAVRSLAALDRWMTERYRKIADRDKVHISSTIALYLYGRSFFLEDYPVAEADQVAFEYWQNQARTHWLKLANRQSQGHLALALKRLGDPQTATKIMASIKERSVTDEELGMYWREQEHSWWWYRAPIETQAVMIEAFDEVMDDAEAVEDCKVWLLKQKQTQDWKTTKATADAVYALLLRGSQLLESDALVEVTLGETTIQPQNVEAGTGFYQQRFTGSDILPEQGEITVRKLDDGVAWGAVHWQYLEDMTKVTAFEGTPLTLQKKLYVKRNTPQGPTLTEVEGPLEVGDEVVVRIVLRSDRDMEYLHLKDYRGSGTEPVNVLSSYRYQDGLAYYESTRDTASHFFIDYLPKGTYVFEYSTRVQLRGEYQTGFAEIQSMYAPEFNSHSESLPLVVQ
>NZ_CP036262.1|WP_145349445.1|101681_103064_+|BBP7-family-outer-membrane-beta-barrel-protein
MKRIFQVLALAAAVTGVSIGNVSNAQTVSVGDMSSYTPPSEAYPSIDASVGGYVGDLATPAGHHERVQRLAPRVASHGGYETCGGCNSVSCEGGCYSSGQSRRGKIGAALNDPCASGWMNAELLLWFPQALQSPDLVATGPNAAGAIQGGPGYQALFGGRIEQGMQPGFRADVGRYFSDGQFGVGARIWFLQGADTAFSAQSDGSPGSPILSRPLFNTSVGTEGGFLVGGPLGPLTGEINISSQLDMVASELYGKALFIQGEDYRMDLIGGYSFFNIENDLLITQSSTQLPPSPAARRVVLDSFNTENNFHGGQIGFQTELNRGRFSFLSLTKVHLGNMHQRVDVFGTSRSDFVGVPASLQTFDRGLLVGDDQQSQSRDVFAFAPEANLKIGYRMRNHVNFTVGYSFIYWNRVALAGDQIDRNVDQTAVLTNNPSTSPARKFNDRGFFVQGIDLGISVDY
>NZ_CP036262.1|WP_145349444.1|99381_101466_-|preprotein-translocase-subunit-SecA
MPSSDPDQPNRATDSIDATDTDPATDSEASESSGGAPPTRSDGRDGVSSQLGSVFTTGASPRMLRWRRKLVQINELEPELTGEDDVTLRKRSLALRYRAMSGEKLASLLPEAYALVREAGRRALNMRHYDVQMIGGICLYEGCVAEMQTGEGKTLTATLPLYLHSLSGKGAHLATVNDYLAKRDAEWMTPLFERLGLTVGIIQTADDQPSRRKSYAASVTYGTAKEFGFDFLRDRLLLRAQNRLQTEMLGDGADGFSGSGDQPVMRGMHFCLVDEADSILIDEARTPLIIGSIEDTVRDQIVETYRWGAEHAPEYELDEHYIIDDETKQYELTAKGRQKVRSIKKSDLVRTVGLVDLYEFAERSIKVHAEFLKERQYVVRPGEQGKPEIVIVDEFTGRLAEGRKWRDGIHQAIEAKENLEISVPTGQAARITIQDLFLRYPHLAGMTGTAATSAREMKKIYRTPVIRVPTNRPPRRVRLKDNVMGDIEKKFAAIVEETVEMNQTGRPVLIGTRSIDKSVRLSQLLTERGIEHKVLNANNVEAEAEIVEQAGGEGKVTVATNMAGRGTDVKLAPGVESKGGMHVICTELHDAARVDRQLIGRCGRQGDRGSYRQYLSLDDDILKGGFGPDKAERLKRIGETATGELPAYAKLFTKAQRKVERKHFRDRMVLLHHEKERKKMQREIGQDPYLDTPD
>NZ_CP036262.1|WP_145349443.1|94584_99258_-|PQQ-binding-like-beta-propeller-repeat-protein
MVSTEMPKQNYPLVLKIVAITCFMVTAADAQNVFRPIDTSGGFIEAPRAIRQQLSESERAISEKRYSDAVLGLGKLLQRSNELGLEEDIAGQDFFLDANEDLDSIAIKSLLRRAEDQLGALPPEGLELYELNYGAAARKELDAATTNRDWNGLRDVVRRYFHTKAGYQSAYLWGYHELATGRPLAASVRFGRLATQPNAAKQLGGQLDVALARSLQLANRDPKQITAAMRPVAGQSPATDGSDSQQQRAKEYKIGEATVPAAEVGNESDWLEEHFAKLQRSSPPIPMDYPVAGGDASRSLNEGGQKPLSSERWLLPTTSGDLETRTIRDAAQAFASQGELPPPSWLPLRVGNQLLMRTTERLMGVDFETGKRTWEYPWESAAPKETSMSVGEEISTDSDQLNQRVWYDLPYGRISSDGKRVFLLEDLGKVQTVQAYPAFGFQPIRQGVSDRKNAGSNTLVALNIESEGKLLWQTGVGEEIPSIYTEAFFLGPPLPVNGQLYVLAELEGDIFLLCMDPKTGTPLWRQQILAMEAGGIENDPIRRISGAMPAYQDGVLVCPTSAGAVVAIDLASRSLLWGAKYKRSRSITNPRNMNSSVDSNRMMQRWYDGTPQIVDGTVYITPVDSDRLHALDLLTGKPRFPEIQRSDMRYLAGIRDEQIIIVGTREVHAYEVKTGRRRWTTALNESGQNAQVSGLSTFGGNLLFVPMSDRQIITIDLAQGIITHRQPTNFELGNLLQAGGQLISQSPTEVAVAFGQQWLRPTVEEHLAQNPKDLWAIKRKAQLLIEDGQTEDALEWLATAREIAPQDEEARSLSVTAMLGALRSDFESHVDLLAPLQTLVRMPNRQAEMLALMARGNVQQGHPLKAIEQLIEHSSLLIQESNLLTDAEPIPTADSYAHPSLDSWIAGQVRKSFEIASPEEAEEMNQAVSLHLETAYSKSTRAFERALHHFSSAAGANAGRLKLVDRLIREDAGLRAERLVKAALLQSDLQPAQESEFRLRLAEIYAQGNFREDVQEQLALLSSDDLDEGKQAILANLQAQIQSDKPITWPAHVHTRWNDSQQRIGTPPAPELLEILAQQGAHLQGWQIVTEEGKSLSLRDPQGRITAIPMDHRDNRSQGQRIAVLDGGLMVALMPTELVAVDLFSASQGSRDSVLWRHAWRNELGGRIARHNTFGTPFGDHYKTYEIDDPLRNSPKGEYRLGPIMENNLYILNAGDLQAIHTISGTRQWSNSGAPRTGHILASPQQIAVASPQSGDNRIDFFSTADGMKVDSKPWPAGEKIWSTAGRNLLTYEETKDAKEIVVRLRDLFADKIILEESLQGPETAGDKIKGDITDGRWLSILHPEGKVIVWDLVNGSEVLSEEIEPIEKLSGLQAVARGNRLILLPETSMPVERVPNTVPLIAQSENHVRVDGPLIGIDLKAGKIAWNVPLEDGPWGCTVGQATGSPLLIFSRALMIHSPTRTGPPTRELSLLAVDIQTGETKAKRTNLRIRSTGNDVATLLNVDTNEKVVAAMVGASFMQFMYSDDPPPETPEAEAPNADELDEDENFNEPFGIFN
>NZ_CP036262.1|WP_145349442.1|93976_94399_-|hypothetical-protein
MSMVNDGFGPNPNLPQQAPKKSNALKWVLGILAVLGVTGLLCCGGCLLMAKMGFDQVGKQIVAQVENDPVIVEHLGQNLTASMEIMATGELQQATGDSDAMSFAISGDKGSGQLTGTQVGPNQFGNFVLIKDGQSYPLGK
>NZ_CP036262.1|WP_145349441.1|93481_93913_-|peptidylprolyl-isomerase
MKVATFDTARGEIRIQLHDDKTPKTVANFEKLVADGFYDGLVFHRVIPDFMVQGGCPQGTGTGGPGYKFEDEFHAELTHDGPGVLSMANAGPNTNGSQFFITHVATPWLDNKHSIFGKVLEGQDVVDSIEQGDKINKITISEE
>NZ_CP036262.1|WP_145349440.1|92571_93318_+|MIP-family-channel-protein
MHPYVAEFVGTTFLILFGNGVVANVVLPKTKGNSGGWIVIAAGWGLAVFIGAFCANEFSGAHLNPAVTLAMYLAGGLSLPDSFGYVGAQMLGAMTGALLVYVFYREHFRQASDDPNAMLACFSTSPNIRNLPQAFVCEVIGTFALILPIFLLVAPGFSSGVEPSDGDPVLGLGSIGLLPVGLLVLGIGLSLGGTTGYAINPARDLGPRLIHALLPIKGKQGSDWQYAWVPVLGPLTGAALAVLVNAFL
>NZ_CP036262.1|WP_145349450.1|113013_114627_+|DUF1559-domain-containing-protein
MSIVPFRLLLGTGMLVLSSLTLPAQEDGPKKLSAEFVPDNALAAIFASPNKVMQEPGFEMLPIEIVRAQGLATVGVDPMHIDRLTVVVGPPGPQGPVGGIVIQFSQDYSIEDLNPQVFREVEPQEINGREVYLLDGPPDTVLFRKDARTFIVGIGNYLNSIVEGNQGQGSLARLLPRIPDQNGVTAVAVLDQVRPMLTGMLKQNARQMPPQLQDIVRLPELTDALIVNIRPADLLNFQATVVALCTDADAAQNAAEILNGSIDFGRNQFLGEVTKDMDLSDPVQKASSEYMFRVSEKISDNLRPQVIDNRLVIKPDSNVGTVGVLVGMLLPAVQAARGAARRMQSSNNQKQILLAMHNYHSTFNHLPDAAVKDKDGKPLLSWRVSILPFIGENELYEQFHMDEPWDSEHNLPLSKKMPAIYRHPSLKTEENETVYQVAVGDGLLFNDQKPTRFRDILDGTSNTILLTETDAEHAVNWAKPEDSPIDMDDPKGHLNIMPGGVFQVGFADGSVQAISELVDPNMLKAMFTRDGREVINR
>NZ_CP036262.1|WP_145349451.1|114669_115740_+|tetraacyldisaccharide-4'-kinase
MDYRSLMNGQRRDPLAFVLRPLLRIGSWFYGLGIRIRNSRYDRGVSETHDAGVPVISVGNLTTGGTGKTPLVCYLARELRSQGFRVALISRGYGRGDGDLNDEALELELRLPDVPHVQDPDRVAAAAVAVEELETEILLMDDGFQHRRLQRDLDIVVIDATCPFGYGYLLPRGMLREPIASIRRADVAILSRCNHISPEERLQIKQAYLRRKPDLIWLEAEHHPGRLVDHENRPEPLEVVAGKRVLVFCGIGNPAAFAKTVRDCGAELVDQLSLPDHASYDREMLERLRAWGESWPPGEIEYMLCTQKDLVKIRTNRIAGIPLRAIQIDMTVEPEAELQQALKKVVQPDGPVEGTV
>NZ_CP036262.1|WP_145349452.1|115863_116157_+|hypothetical-protein
MGWFRRRRDSSPDAPLVPCPHCGADVRADAVACRECGYAWEADDLVDDGSDDFDYDAFVEREFSESNVSQSLPAWQRFVIFLLVLAFAATLLGPLLF
>NZ_CP036262.1|WP_145349453.1|116188_116707_+|SET-domain-containing-protein-lysine-N-methyltransferase
MSGLSKKRRAKLQQKLDEDYGYRQYADRDVEVREGACGHGVHAVRQFLPGELVIEICGQVLSQKKYDGSTYVMEMDDEWYLEPTIPGAYLNHSCNPNAELLKLTDSSMGIIAICNIEPGSEITFDYQWTAGDWVPRCQCGAPNCRGWVVGADSLEEMKEFAKEQKQKSKRKK
>NZ_CP036262.1|WP_145349454.1|116826_117441_-|hypothetical-protein
MNRNLPSLQSFHRIIGVSCCALLAIGACFADEPASEASALSELSVAPLQHQFYPDDRPEWIVADPVLEGPQHRWAVASSPALTEEASMTSLTEQKRIAVAAYLSEVLGTTDPPFKIDDQQIDRQLVNPDRIYHGEVTTSDGVMYEDAVELVFDQDFRDGIQKKWRRYERRSRLAGLGVLGAGGFALLLGMTGVLKVVSRSRASA
>NZ_CP036262.1|WP_145354834.1|117509_119540_-|protein-kinase
MAALAGTLDRGRRLFGRPNAADTPTSAFDNTPSDSASSPPIPTAPKMHFTYASGSSPLPRYTIRRGVGIGGFGEVYFAVSEAGKEVAIKRIQRNLDVELRGVSHCLNLKHPNLVSLFDVCRDDQDQAWVIMEYIAGPNLREVLDQHPQGLPEEEVRRCLVGLASGIAYLHDSGLVHRDLKPGNVFDDAGIIKIGDYGLSKFISASRRGGHTESVGTFHYMAPEVGRGEYGREIDIYALGVILCELLTGRVPFDGESSHEIVMKHLTAQPDLEGIASPYREVIKSALEKDPRNRPQSIAQMLKPLGLQIDTFGSGTPATMPSSLGSTSSPAESKQDPILARLASPPAAPGASAEKPIREEPLARAIRGSLTDLARWWESLESYPGTRIAMMFMIVALVVINTGWLVPLLTFVAIFYVPYYIIRHLVLGIRQQPSYAEAHQLAVARAQIPRPLSAGQWRQQKRIELASKRSLTRMTELSGSWTKAIFWTAILGVVGTMIGLRDADLSAENIAPYALTAVTIGFAALALLGMGKLWERGEGEPLSRRLVLAGVGIIVGSFAYVASEYLLLPIGGTALSADVADNLPQNLYTNEGVPRLAAMMAHFALLMGAVGWWKNTDPLRKRRLSVWTVAVAVVFEWAISLALPIPQPWGILVAGGIAIVLQLASPWENRHQEMQVS
>NZ_CP036262.1|WP_145349455.1|119668_120304_-|hypothetical-protein
MHSHSLSTEPSNQSGQPDRWALWVDGAGGFLLITSLSATIGGPASDDEAMIAVQADLRRREALITRSNGQYQVQAVDGRVAPSASASGNRESASPQAVVSLRPEDSFVLGDGVPFKFRLPNPLSGSARLTVDRRYRFRSHVDAILLIDDTLVIGPSADCHIQVPHAAGKLVLMPKENAWQIKPAVAGTQWQNLQCGTRWHDFDLSMTLEKL
>NZ_CP036262.1|WP_145349456.1|120561_121371_-|hypothetical-protein
MLKKIILAGSAVTLLTGMAMGTGLWSYGRCAADKVTQSAKDLVPMEWEVDRARKMITDLEPEITENAKRIAREKIGVTRLERQVDESSARLADAQRNIERLSSDLKSGDQAYTYAGKTYTSVQVKDDLSARWKRFKTQRATVDKLEQQLDARHASLAAANERMDAMLSAKRQLEVEVENLQARLSALRVAQTTSDLNLDDSQLSRTRELLDELATRIDVEEEVMAVDADYFGEIDLDEPEQEDLLDEISTYFGGDADDDQQLVSIEMVQ
>NZ_CP036262.1|WP_145349457.1|122487_122703_-|hypothetical-protein
MTDKIHAHDAGTPGPRRPFLGVMFRCCNVYARIYRRVDLTAYAGNCPRCGKALQVPIGNGGTGQRFFSTKQ
>NZ_CP036262.1|WP_145349458.1|122727_123279_-|sigma-70-family-RNA-polymerase-sigma-factor
MSKEAELIEAALQGDKEAFGQLVRTHQDRLFAAMLQVTRSAEEAEDVVQDAFVRAYLKLDTFQRNSRFFTWLYRIAFNSALSRRRRKRVTMSLDQTREVTGNEPIDNVDSPDERMLRGERVLSIQVALDQLSDEHRTILVLREMENHPYEDIAEILEISIGTVRSRLSRARTQLRLTLEGMQQ

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Crispr_ID: NZ_CP036262_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_2

152828-152946

Orphan

Consensus_repeat	Method
CAGTCCTACACCGTCCAGCGCCC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP036262_2

>merge|NZ_CP036262|2|152828-152946|CRISPRCasFinder
CAGTCCTACACCGTCCAGCGCCCGGTCACCGAAACGCAGTACCGCGATCAGTCCTACACCGTCCAACGCCCCGTCGTTGAAACGCAGATGCAGACCCAGCAGTACACCGCGCTCCGCCC

>NZ_CP036262|2|2|152828-152946|CRISPRCasFinder
CAGTCCTACACCGTCCAGCGCCC	GGTCACCGAAACGCAGTACCGCGAT
CAGTCCTACACCGTCCAACGCCC	CGTCGTTGAAACGCAGATGCAGACC
CAGCAGTACACCGCGCTCCGCCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354837.1\|159398_160499_+\|patatin	unknown	unknown	gnl\|CDD\|132838
NZ_CP036262.1\|WP_145349472.1\|154208_154553_+\|rhodanese	unknown	unknown	gnl\|CDD\|238089
NZ_CP036262.1\|WP_145349473.1\|154884_155541_+\|ribonuclease-H	unknown	unknown	gnl\|CDD\|260015
NZ_CP036262.1\|WP_145349466.1\|140004_140682_+\|redoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239245
NZ_CP036262.1\|WP_145349471.1\|151260_152016_-\|lipoate--protein-ligase-family-protein	unknown	unknown	gnl\|CDD\|319742
NZ_CP036262.1\|WP_145349475.1\|157308_158295_+\|IS4-family-transposase	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349467.1\|142079_144551_-\|MMPL-family-transporter	unknown	unknown	gnl\|CDD\|223964
NZ_CP036262.1\|WP_145349477.1\|163372_163858_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131309
NZ_CP036262.1\|WP_145354838.1\|165793_166012_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349464.1\|136371_136764_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349463.1\|134485_135379_+\|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|223730
NZ_CP036262.1\|WP_145349479.1\|166524_167574_+\|replication-initiator-protein-A	unknown	unknown	gnl\|CDD\|370826
NZ_CP036262.1\|WP_145349476.1\|161600_163382_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238760
NZ_CP036262.1\|WP_145349474.1\|155802_157035_+\|tyrosine-type-recombinase/integrase	unknown	unknown	gnl\|CDD\|271175
NZ_CP036262.1\|WP_145349478.1\|164291_165593_-\|IS256-family-transposase	unknown	unknown	gnl\|CDD\|307151
NZ_CP036262.1\|WP_145349469.1\|146284_149512_+\|organic-solvent-tolerance-protein-OstA	unknown	unknown	gnl\|CDD\|224369
NZ_CP036262.1\|WP_145349470.1\|150057_150954_-\|TonB-family-protein	unknown	unknown	gnl\|CDD\|367555
NZ_CP036262.1\|WP_145349462.1\|131455_134434_+\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223354
NZ_CP036262.1\|WP_145349468.1\|144606_146046_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224720
NZ_CP036262.1\|WP_145349465.1\|136898_139658_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145349478.1\|164291_165593_-\|IS256-family-transposase	gnl\|CDD\|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	4.50503e-29
NZ_CP036262.1\|WP_145349472.1\|154208_154553_+\|rhodanese	gnl\|CDD\|238089	cd00158, RHOD, Rhodanese Homology Domain (RHOD); an alpha beta fold domain found duplicated in the rhodanese protein. The cysteine containing enzymatically active version of the domain is also found in the Cdc25 class of protein phosphatases and a variety of proteins such as sulfide dehydrogenases and certain stress proteins such as senesence specific protein 1 in plants, PspE and GlpE in bacteria and cyanide and arsenate resistance proteins. Inactive versions (no active site cysteine) are also seen in dual specificity phosphatases, ubiquitin hydrolases from yeast and in sulfuryltransferases, where they are believed to play a regulatory role in multidomain proteins.	1.09432e-27
NZ_CP036262.1\|WP_145349473.1\|154884_155541_+\|ribonuclease-H	gnl\|CDD\|260015	cd13935, RNase_H_bacteria_like, RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner. This family includes bacterial ribonuclease H (RNase H) enzymes. RNases are divided into two major families, Type 1 and Type 2, based on amino acid sequence similarities and biochemical properties. RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner in the presence of divalent cations. RNase H is widely present in various organisms, including bacteria, archaea and eukaryotes. Most prokaryotic and eukaryotic genomes contain multiple RNase H genes. Despite the lack of amino acid sequence homology, type 1 and type 2 RNase H share a main-chain fold and steric configurations of the four acidic active-site residues and have the same catalytic mechanism and functions in cells. RNase H is involved in DNA replication, repair and transcription. One of the important functions of RNase H is to remove Okazaki fragments during DNA replication. RNase H inhibitors have been explored as an anti-HIV drug target because RNase H inactivation inhibits reverse transcription.	1.19533e-58
NZ_CP036262.1\|WP_145349466.1\|140004_140682_+\|redoxin-domain-containing-protein	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	7.74965e-30
NZ_CP036262.1\|WP_145349471.1\|151260_152016_-\|lipoate--protein-ligase-family-protein	gnl\|CDD\|319742	cd16443, LplA, lipoate-protein ligase. Lipoate-protein ligase A (LplA) catalyzes the formation of an amide linkage between free lipoic acid and a specific lysine residue of the lipoyl domain in lipoate dependent enzymes, similar to the biotinylation reaction mediated by biotinyl protein ligase (BPL). The two step reaction includes activation of exogenously supplied lipoic acid at the expense of ATP to lipoyl-AMP and then transfer to the epsilon-amino group of a specific lysine residue of the lipoyl domain of the target protein.	1.10145e-44
NZ_CP036262.1\|WP_145354837.1\|159398_160499_+\|patatin	gnl\|CDD\|132838	cd07199, Pat17_PNPLA8_PNPLA9_like, Patatin-like phospholipase; includes PNPLA8, PNPLA9, and Pat17. Patatin is a storage protein of the potato tuber that shows Phospholipase A2 activity (PLA2; EC 3.1.1.4). Patatin catalyzes the nonspecific hydrolysis of phospholipids, glycolipids, sulfolipids, and mono- and diacylglycerols, thereby showing lipid acyl hydrolase activity. The active site includes an oxyanion hole with a conserved GGxR motif; it is found in almost all the members of this family. The catalytic dyad is formed by a serine and an aspartate. Patatin belongs to the alpha-beta hydrolase family which is identified by a characteristic nucleophile elbow with a consensus sequence of Sm-X-Nu-Sm (Sm = small residue, X = any residue and Nu = nucleophile). Members of this family have been found also in vertebrates. This family includes subfamily of PNPLA8 (iPLA2-gamma) and PNPLA9 (iPLA2-beta) like phospholipases from human as well as the Pat17 isozyme from Solanum cardiophyllum.	9.8386e-51
NZ_CP036262.1\|WP_145349467.1\|142079_144551_-\|MMPL-family-transporter	gnl\|CDD\|223964	COG1033, COG1033, Predicted exporters of the RND superfamily [General function prediction only].	1.23502e-64
NZ_CP036262.1\|WP_145349477.1\|163372_163858_+\|hypothetical-protein	gnl\|CDD\|131309	TIGR02256, Uncharacterized_protein_y4qB, integrative and conjugative element protein, VC0181 family. This uncharacterized protein is found in several Proteobacteria, among them Rhizobium sp. NGR234, Vibrio cholerae, Myxococcus xanthus, and E. coli strain ECOR31. In the latter, it is part of an integrative and conjugative element that is readily induced to excise and circularize.	2.47528e-11
NZ_CP036262.1\|WP_145349476.1\|161600_163382_+\|hypothetical-protein	gnl\|CDD\|238760	cd01483, E1_enzyme_family, Superfamily of activating enzymes (E1) of the ubiquitin-like proteins. This family includes classical ubiquitin-activating enzymes E1, ubiquitin-like (ubl) activating enzymes and other mechanistic homologes, like MoeB, Thif1 and others. The common reaction mechanism catalyzed by MoeB, ThiF and the E1 enzymes begins with a nucleophilic attack of the C-terminal carboxylate of MoaD, ThiS and ubiquitin, respectively, on the alpha-phosphate of an ATP molecule bound at the active site of the activating enzymes, leading to the formation of a high-energy acyladenylate intermediate and subsequently to the formation of a thiocarboxylate at the C termini of MoaD and ThiS.	5.64857e-15
NZ_CP036262.1\|WP_145349463.1\|134485_135379_+\|alpha/beta-hydrolase-fold-domain-containing-protein	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	5.27231e-16
NZ_CP036262.1\|WP_145349479.1\|166524_167574_+\|replication-initiator-protein-A	gnl\|CDD\|370826	pfam10134, RPA, Replication initiator protein A. Members of this family of bacterial proteins are single-stranded DNA binding proteins that are involved in DNA replication, repair and recombination.	4.55633e-98
NZ_CP036262.1\|WP_145349474.1\|155802_157035_+\|tyrosine-type-recombinase/integrase	gnl\|CDD\|271175	cd00397, DNA_BRE_C, DNA breaking-rejoining enzymes, C-terminal catalytic domain. The DNA breaking-rejoining enzyme superfamily includes type IB topoisomerases and tyrosine based site-specific recombinases (integrases) that share the same fold in their catalytic domain containing conserved active site residues. The best-studied members of this diverse superfamily include Human topoisomerase I, the bacteriophage lambda integrase, the bacteriophage P1 Cre recombinase, the yeast Flp recombinase, and the bacterial XerD/C recombinases. Their overall reaction mechanism is essentially identical and involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA. The enzymes differ in that topoisomerases cleave and then rejoin the same 5' and 3' termini, whereas a site-specific recombinase transfers a 5' hydroxyl generated by recombinase cleavage to a new 3' phosphate partner located in a different duplex region. Many DNA breaking-rejoining enzymes also have N-terminal domains, which show little sequence or structure similarity.	8.38353e-23
NZ_CP036262.1\|WP_145349469.1\|146284_149512_+\|organic-solvent-tolerance-protein-OstA	gnl\|CDD\|224369	COG1452, Imp, Organic solvent tolerance protein OstA [Cell envelope biogenesis, outer membrane].	6.77636e-06
NZ_CP036262.1\|WP_145349470.1\|150057_150954_-\|TonB-family-protein	gnl\|CDD\|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	1.80518e-21
NZ_CP036262.1\|WP_145349462.1\|131455_134434_+\|FAD-binding-protein	gnl\|CDD\|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	3.97409e-76
NZ_CP036262.1\|WP_145349468.1\|144606_146046_+\|hypothetical-protein	gnl\|CDD\|224720	COG1807, ArnT, 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family [Cell envelope biogenesis, outer membrane].	6.73686e-10
NZ_CP036262.1\|WP_145349465.1\|136898_139658_-\|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.	8.19715e-106

>NZ_CP036262.1|WP_145349471.1|151260_152016_-|lipoate--protein-ligase-family-protein
MPQLLERSLDSPASNLALDEALLLAAEADEIPPVLRLWQFASPTVVVGRGSKATEEVQLEHCRSQQIPILRRCSGGATVMGGPGCLMYSLVIDLRPNPHLRQLNHLHSHVMQRVLAGVQKSVDSDQKEALQFQGICDLTYQNRKFSGNSLRITRHHVLYHGTILLASDLGLIAECLATAPRQPTYRQERSHRDFITNVPANANSLRTHLAKEFEAQEPLCKDHEPLPSTLEERIRKLTEERYGQESWTLRH
>NZ_CP036262.1|WP_145349470.1|150057_150954_-|TonB-family-protein
MESPFIVPLQLETGPISPTVGHGASAWSASLILHAAAAILGISIGVRESIDVPVTPGETGSQAVIQLAAAQVTASAATAVLVPWGDPESDSSSPPPTLETSGEAPREIEPLLAELPAVLLPMTFTEIELPVDSVPKGDPNGQPGPEVIPDSEPPPIVEAMPESDSEAEVADANVQAAQDAHEEIEASMPAAEAPATVASTSAPSGAQVDTPARPAPSNPPPVYPPAADLENRQGRTILRVEVDSKGKANKVEVIQSSGHKDLDNAAVAAVRNWHFLPAMKGETAVAQTIAVPIRFVDP
>NZ_CP036262.1|WP_145349469.1|146284_149512_+|organic-solvent-tolerance-protein-OstA
MSALPAERNDREVEGCSEPRSPTSLSAARRRSCRSLLVASLVMIIGWLGGADAYSARPAETQAAGLRVRGTTVWRWRDGATDLYFLTGDCEIESNGKAILADRVLVKFDRRGDAFDVVALASGSVHVDGQSQQEWSQQVTLSQRPSIDGLQYRGRPEQPLELLARMTQLQGQPIQGQPIQGQPHGRFGQVQQAQLMTPIPAANSAAYADGGVQQAVGIFDPAEPLQATSPIRPVQFQPPVEREGPLGDNNMRFLVGGGALAVEVLPRNASLLPQISIRTRPLPGETQGESVIIGRGGVTIAINDAQADLGDRIINVGTVSLSADRVVGWMPNLSSVLSGGGLGAGDGELYLEGDIVFRQGDRVIYADRMYYNVTRQYGMVLDAEVLTSIPEYEGLVRLKADVLQQVSQGEFVAFDAALTTSRMGVPRYWLQSEQLRLSTREELVVDDATGLGTMTRRNLVSSNRNFVYAGGVPLLYWPVFTSDLKHSNLYVTDIKIKNDSIFGTQLFLDFDLFQVLGVDDPPDNVEWTLSTDYLSDRGPALGTTLDYNVPSVLGIPGPVKGMFDIWGIDDSGLDYLANDRKNLVPPVSLRGRALLRHRHYLPNDFELIAELGLISDRNFLEQYLEREWDRDKDQDNSLRLRKYYQNNMFDLNVSVRTSDFFMDTNQLPRFDHYGLGGSIFGDRLTWSMHNQIGYSKLEVADAPEDPVELAKFTLLPGEVPAEGLIASTKQELAAPINAGVVKVVPYVSGEVTYYGEDVNGNELTRLLGQGGVRTTLPMSKQFPTVQSSLLNIRSLAHKLEWRGDFFYADSNTDLDQIPLYDQLDDDSQEQFRRRLIFDNFGGPPLPTQYDPRNFAFRQGMQSHVTSPSNPIADDLMQVRLGLNQRWQTKRGLPGRERIVDLAIFDFDVLLFPEEDRDNFGEVLGPTRYDFRYHVGDRVTLLSDGYFDFFEEGLRSVSAGVMSSRPGLGDIYVGFLSLEGPISSSVLRGAVDYRLNEKWILGAGSTFDLGVVGNVGQNLTITRIGESGLLRMGINVDSGRDNVGFVFSFEPRFWPKRRLGMLGGQLIPPPGVEGLE
>NZ_CP036262.1|WP_145349468.1|144606_146046_+|hypothetical-protein
MKNDPATSQSDWSFSSLKVWRSLWGLLLVALVIRGGILVSRVDSLQADVDGYRWIAETLAEYQVFGVAGEEGNVRATAFRPPLYPWMLSWLVSDSPTDAGATGESKPTVSIWSVVLLHLILGLLTVAGTYHIARALLSPLEAWGAGLLVAMDPILLTQSTQVMTETLATALAVAVGLAWQRLFLPLESSHTDDQAAANNPFARPRYWLASGGLAVALSLGFLSRPTFFVWAFLLLIYLVGVAVRKRVWWPVVTAALVVAVMASVIGAWTVRNQRQLGHPVWATSHGGYTLLLGNNPLFYDYLEDDPEQPNQTDAWDAERFHRTWAGRYQSDPLEEDFWKWPPTGPVPSPQIDDEVADDALAYSAAKQTIHQRPAMFAWACCVRVARLWTPLPHATPGRSLNAVRAVGGYYFIFYAAMLGGLCRYGRRWLHSPWMAGLLLAVALTCLHSIYWSNMRMRAPVIPWMACVAAAAIGSREPRR
>NZ_CP036262.1|WP_145349467.1|142079_144551_-|MMPL-family-transporter
MLQETPLQSLVRQWVALRWWLLGIGIVLYLVTLPAAGRLQMDRQIESMFPASDPAVVAYKDLAEHFGGNAIVLLVYPDDQLFTAGGLQRAAKLSDRVGAVPGVQATLSIAEVAQSVEELRGISSFGMALLGEKKPPAILETSPTSIAFRKMFAGYTHNQAENYGAIVVMLQPLADPSSETPDKRSGGVQANHEATVASLRAIANDLPPELGKGVLVGQPVLVSEGYTMIQRDGQQLGTTTIWLLSVVLLILFRSPRWVLLALATIWGSSTVTRGLAVLLGLQLSLVSSMLTAILTVVSVAALIHIAVAWQKRRARGEDRQAATIRTLTRLLPPILWAGFTDAVGFAALMAADVGPVRDFGLLMTLGVGVVMLVLFFLLPAGLCAGKPETAHGKGSPQHAHQANRSKRRRRFTAGFGRWGSRFTVGLLKHRQAILWGTCLLGLLTAIGLSRLSAETNFLRNFREESSIAKAYQLVEEQFGGAGVWDILLPIPDRPLTTADLKRVHNLEVDLQAIRIPDFPNARVTQTLSMADTDAAAALSENPLIRLAPSSVRLQRMAQIMPEFSAALMTPTDSNDGYHGLRMMLRSPENLNSEAKTALIRSVQQTVQQHLDRPEWQSVQQRPKQTGLEESAFTEPGRVTGYYVLLARLVNSLLEDQWTSLGLASIGIFVVVWWATGNFVWAALTLLANGFPVMISLAALGWLNIPLNMGGAMIAAVSIGLTIDGSLHFLASYRRSRQRYGRCAGRAVLRAQSQVSWPISCATLALVVGFAVLTRSDFVPTATFGALLSLAMLLGMLANQILLPVLLGRAIFSSKLLFPSDDEF
>NZ_CP036262.1|WP_145349466.1|140004_140682_+|redoxin-domain-containing-protein
MMLTSHNKRYLVLGILAVSGLTGCANRGRIPFFSQAPEPESLETAESSPSYALSDTSESSPAAVAAAEMSMSDLESTESPKEQAPADVQVKTVSATMESKAEVASADLEKPAVVSRSMIQPTLITLPEGADLEALVAETRGPVLIDFYADWCGPCRTQGKILHSLESEAASRQGRIIKVDIEAHPKLAKRLGVKSLPTLVMIRDGEVVERKVGVTDKKTLLNWLK
>NZ_CP036262.1|WP_145349465.1|136898_139658_-|protein-kinase
MDPSTQPSSSADDPGPDSEPDREIAASSETESTKPVLPRLSPALPADTSTEEIPGQDLTPPDQGSAADLPIDDLVAAKTVIRKANGDGQSPLAGHTPAQIASVLLGYHLNHFQLNSLIGGGGMGAVFSAHDTRLDRTVAIKVIPRVGEDPDLLRRFRNEAQSAAKLDHPNIARVYDVGRHDEWHYIVFEFIEGTNVRDLVNRHGVLSIDEAVYFVRQVAEALEHAHLRGVVHRDIKPSNVLIRPDGQVKVVDMGLARTLQLEVSGDMTASGVTLGTFDYISPEQARDPRDADVRSDIYSLGCTLYFMLTGSPPYPGGTVLQKLLSHGNSPPPDPRDVRPEVSDDLVSILHKMLAKRPGDRYRRPIDLISDLAELARRENLTRSQGLSTVAISTGSSWLARLERHLPWITAAVLLVLSVAWLQLLSSVSAVDDSMPRPTSMASEPTRMASLRPKETNQPATDLLRKPSNMGEDLLATKPLVGPPAPSSSDEATQPPSIQQIPLPPGIVPETTRLEENLPSGAAMSSTISELTATRIRVGGISATTPDELRTNDLATALALANEHKIARIELAERLIVTEPLVIEQNNLVIAASDPGCQIQFENSPLLAMEHAVMVDIGSQRVRFENLQFVWKVPSNAVHGGALFRIAANRGVQFENCAITIENTFLRDPINAFWITPVPTSSEDQQTVSAASPPLVAIELLNVIVRGEMTLIRMDVAAQLQFRWENGLAAISQRLLETGGAITKPPAGRTQLKLVLKQITASLPTGLAQVNLGPSGSIPVVLDRVCTNSVFKTAPGFSHIEINGLSNLQDGPFVLLGGIGNHYDSGPGNSDQMVRLNDQADDSVLFRLSDLATNTPPAWMKEQAPQSIIHWSQPSPPSEKPLHLLTPEDFLQDGTVLPGFDIGLLPTLLPSATTPPDDPT
>NZ_CP036262.1|WP_145349464.1|136371_136764_-|hypothetical-protein
MKRFALMALTLMMLGSPAYAISEFNKQWKAQYLGDDASEDFKRSGRKAGCYVCHVKGEKKDEARNEYGNALHKHLDAENFSKERIKAEPEKVKAEILEAFKKVAPVKSKDGKAFGEKIKAGELPATDAKL
>NZ_CP036262.1|WP_145349463.1|134485_135379_+|alpha/beta-hydrolase-fold-domain-containing-protein
MPTKFLLPFLTSMLLLPSTLVFAQDRAEIPLWPAAAPGETGDVEPEHALPKRENENPPKLRIGNVSKPVMTLFKPENPDPKGTTVIVAPGGGYSILAYSHEGSEICEWLNSIGVTAVLLKYRVPRRSEENFHELPLMDAQRAIRMVRSKAAEWNINPDRIGMLGFSAGGHLTVMAGTNGGKASYEAVDEIDQLSPQLNFMIPIYPAYLLNKKTNQLNTNIVVNKDIPPAFIAITFDDSERAVGAAMLLVAMKKVDVPCELHVYRNGGHGYGMRASKNAVSKWPELCRDWFAASGLIE
>NZ_CP036262.1|WP_145349462.1|131455_134434_+|FAD-binding-protein
MINASEDPATNDTIDSSELQRLLKQGIRGEVYVDDVSRGVYATDASLFQMFPRCVVVPRDQADLCHAMKIAAAHKISVTPRGGATSLSGQTYGPGIILDVSKYMNQVLAVDVQAQTARVQPGVVRDQLNAAVAADQLHFAPDPATGSRATIGGMIGNNTCGTRSVVYGKTIDHVLACRVLLADGTVAEFEQVEPAVWQARAAGENVSEREAELYRGVTEIISEHHDQILQRYPKVLRRVSGYNLDEFVDGAGYTGTIGPRAEQNQGKRPWNLSNLIVGSEGTLGVVLEATVRLTPLPQASAVCVVHFSELLDSLKYVDAMLQHEPSTVELLDETVMREAKVNSATQHMSHFIEGDPAAVQIVEFFGQDLPEAQRRCEQFATAMKEAGIGYSWPVLSKPSDVHDVWETRKLGLGLISNVRGANKGRDFIEDACVPTAHLAEYISKIQQLCTAQGITRLSLYAHASVGVVHVVPALDLHQHAEAEKMQAIADQAFQWVMEYGGSWSGEHGDGQLRGQYLPAMFGDDLYEAFRQVKRLFDPNNLMNPGKVIDSQTLLDNLRYQPPGYAEAAEKSEQAALYKYADQGGLQLAVEQCNGVGACRKIGSGTMCPSYMATRDEQHSTRGRANALRLAMSGQLEADPLEGLASDGLHDVLSLCLACKACKSECPNAVDMAKLKSEALQIRHDRKGISLGAKVLGRMPDAAKRFAGWTGNIANLTNWIPGGRALLQRMVGIDRRRPLPTFATTTLAQSLQRDPVPTGRRDRGRVVLFDDTYANYFEPNLGRAAIGLLEDAGYEVILAKAGCCQRTRLSKGLVREAKKYGVEVFRRLDVFAQQGLPILCLEPSCASALVDDLPDLLDDRELAQRVAGQIQMLDGFLDREGIEVECTEESILLHGHCHQKATFGTSAIHALLGGPESGCCEEVDSGCCGMAGSFGYEHYDLSQQVGEDRLFPAVRQAVAEGRAVVACGISCRHQLKDCLGVDAKHFVEVLRIR
>NZ_CP036262.1|WP_145349472.1|154208_154553_+|rhodanese
MTNESELPIEIDVQEVQRLRDAGEAFLLLDVREQDEYATARIEGAVLLPLSELQERAKELQERQAERVIVHCHHGGRSLRVVSVLRQSGFKQAQNMTGGIEQWSQEIDSTVPRY
>NZ_CP036262.1|WP_145349473.1|154884_155541_+|ribonuclease-H
MAQKKPKFYVVWQGRSPGVYATWDACQNQISGFSGAKYKSFPSRSAAETAFKQAADQHWGKGGSSRSKKSTPVVDSDDLEGMGVDMTAWAVDAACKGNPGELEYQGVDLASGINLFHKGPYEEGTVNIGEFLAIVHALALLDHAGHSHTAIYSDSRIGISWVKQKKCKTKLPRSPINAGLFRLVDRAEKWLESHKFQNRILKWETKHWGEIPADFGRK
>NZ_CP036262.1|WP_145349474.1|155802_157035_+|tyrosine-type-recombinase/integrase
MAGLEVRNGRYNLILRFGGKRFVRSLKTSDEDEATSKRLRVEENIKLVESGRLTIPDNSDVVTFLLSDGKLDRKPVVKGSLTIPQLFKEFWEALPVDSLEGSTMDMMKIHQRHVESVLGRRLIAQDLTHDDLQKYVTKRAAVKTYKGTTISGGTIKKEIVTFNSVWRWGVNTGKLHGEFPKSNLRYPKSKELPVFQTWQEIERQVAAGASAGIWDALYLSLDEITHLLDHVKEIANLPFLYPMFTFAAYTGARRSELLRSQLSDINLQGGVITIREKKRVKGKTSTRRVPLATPLKAVLTNWLSEHPGSPFTFCHPDPILGSHRKTRDDENQLTRDQASHHFKQVLQNSPWSVIKGWHCLRHSFISNCASKGIDQRMIDEWVGHSTEAMRRRYRHLFPASQSQAMKSLFA
>NZ_CP036262.1|WP_145349475.1|157308_158295_+|IS4-family-transposase
MNVSSLNNARFRRQISFLRRQFLQDGESAFANILADSCIAEALRANDVQWRDRIFSPMVTLWVFLIQVLSADHSCRAAVARLVAHRVSQGKPSCSAETGAYCQARKRIPEKFFADVVRKTGHATVEAADTAWRWKERRVLMFDGTTVTMPDTAENQSDYPQNSAQKPGLGFPIARIAALLSLSCGAVLDLRICKYAGKGQSELGMLRQLMGVFSKGDVLLADRLMCSWREIAMLKARSVDSVTRLSAKRTADFRCGRRIGKDDHIVRWPKPVLRATDPETDCSLPDFLEIRETRVRVEQAGFCTVCIIIVTTLLDSDEITKDGTTNWI
>NZ_CP036262.1|WP_145354837.1|159398_160499_+|patatin
MNLNGQPEQQTTKPLRVLSLDGGGMRGIYSAAYLSRLNDRFAQVHKTSKLIDLGKRFDLIVGTSTGALIGCGLAKGVPLSEIVALYRNNGSNIFRRSIPKTMFGVPLDILKRGKALAVGEKSLREALQLCLGNTTLAEIYRDRNIAMAIPAVEMGRHGSWVFKTAHLNGSNHRDDDYSLVDVCMATSAAPLYRSLARIPVPDSGQTRAYNYFADGGLWANNPVLVGLIDSLGMASEGQEIQIYSLGTCSRPTGENLRPSDVNRGLVGWRFGADAAALSIDAQEMAYDYMARMLTKHVKNTCTIVRFPFDDVPAHMMDYLGLDDTREESMDELVRQAHSDADFTNSKCAKPEDTDGRLIASLFKPEE
>NZ_CP036262.1|WP_145349476.1|161600_163382_+|hypothetical-protein
MNAKNSIAELARWIDALPNTRRLAGHELHNYRKQFVDGWRIDLNLAENVSINLLITAQFPFVSPKIALIDRTKFLSWPHVEKDGCLCVFPPNTNVDPYRPVEVAKSLVAETEALLQCLLDGNLDDDFNREFDSYWLLSSDDLRHQFFSILPDGCDSQKVAVWSSSKFRIIGADEKSVLCWLKNRLQKDYDRTDTGFLVKLSKPLSPEEYPDCTEALLALISEDAPNFLESISDHIAKSFQPLTIILAISATNGTNYGVVELCRLLRANEKVSKCGRSNRVSVNGFRDGKAPLSVQLSQQTKYTKVVRSPLERADAEWALGGRGHDPRFAVLQKQRVAIVGLGSFGSFLTDNLIQAGLGQVAMFDGDLMRWENTGRHLLGGDTVGQNKTDALKRRFETNYPTIVSCESNPVDWQQRIETAESLDGFDLVISTTGSWKAECMLNDLHECSGKRTPIVYAWLEPFAAAGHAVAIMERSGCLQCGFTGAGQFSRRVFDWPAAPTTMVSQAGCGNEFQPYGITDSLHSIAMAVDLSVECLLGQLTASTHRVWINKDRKIDPIQRGWSVAWQTVPNFDTREEVVSEFPWSARPDCQRCS
>NZ_CP036262.1|WP_145349477.1|163372_163858_+|hypothetical-protein
MQLDQPIRYAIANSDQCIVVETQVLEVFDDYRQDRCWKREAGGQLFAKLTNDEIVLKIATSPTRKDIRRRFQFIPFLKNQQEEINSQFESGLFFVGDWHTHPQTVPEMSPEDRESMADCFVKSSHGLDAFLMVIVGTRPFPEGLSVSIHRERDFAKATLVS
>NZ_CP036262.1|WP_145349478.1|164291_165593_-|IS256-family-transposase
MLKVERWSPGEQTLLSTTFQFSSAATDGETIMNEVSLLESLGQVSASETGQIFRNFLRGHVREMISEVMAAEVTELCGPKHDPTSSDVYRAGSSSGRVLYEGEREEVVRPRVRQKFSNGSSHEVELSTYRVAKDPQQLQAQIVQAIVSGVTSRGIEELKPNSPGVKKSNVSRLWKDAGNKLIEQMRGKDLSSITWCALMLDGIHLSKDQTAVVALGIDSGGRKHVLDFALGSSENLEVSRELMTRIVNRGFTCDHRLYVVLDGSDALRGAVVEFFSDAVIQRCLVHKERNIKGKLSKRHWGELSRLFTRLRRVQGIEAAEEIFGELKTFLEPINAEAYRSLHEAGDDLLALHRLNVPNTLHRSLLSTNAIENSFLNTRRRLGRVTRFRAETDQASRWLSYALLEAEKGFRRITGHTSLPLLVAALGRPEVPPA
>NZ_CP036262.1|WP_145354838.1|165793_166012_-|hypothetical-protein
MVEAKAIQEWYDTKTVGEILDRAAYSVREWCRLGRVKAEKRVCGRGSAKEWMISNAELERIKSEGLLPLERR
>NZ_CP036262.1|WP_145349479.1|166524_167574_+|replication-initiator-protein-A
MNETTTTRSPLLPDRHPTHDFFVCDIFNAAPKSDMASMEHPIFSLSTKPDRSIRRYDHGDLFVEIRPSADGLATVHDRDILIYCISQVMAAKNAGRSASQIIRFRGHELLRATNRMTNGRGYDGLKAALERLAGTRITTNVVTGGKEIIRGFGLIDQYEIVRETRGGRMQEVEVKLSDWVFNAVEHHEVLTLSRDYFRLRKPIERRIYELGRKHCNRKAEWKISLALLQKKCGAVSSSREFRRLVNNIVQEDRTYSHMPDYAVDLNDDDMVIFTSRGTIASLTTSSDVDLSHVRISGDGYDQARLAAPGWDIHRVEQEWREWMTESPTNSDAAFIGFCRKWFEKRGRPA

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Crispr_ID: NZ_CP036262_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_3

412108-412211

Orphan

Consensus_repeat	Method
CCAATTTTGCCACCGTCCGTGGCAAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_3

>merge|NZ_CP036262|3|412108-412211|CRISPRCasFinder
CCAATTTTGCCACCGTCCGTGGCAAAATTTCCATCGGTGCCCCCAGCAGTGCAGCAAACCCCGGAAATTGGGGAACTGCCAAATTTGCCACCGTCCGTGGCAAA

>NZ_CP036262|3|3|412108-412211|CRISPRCasFinder
CCAATTTTGCCACCGTCCGTGGCAAA	ATTTCCATCGGTGCCCCCAGCAGTGCAGCAAACCCCGGAAATTGGGGAACTG
CCAAATTTGCCACCGTCCGTGGCAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145349657.1\|407168_407501_-\|thioredoxin-family-protein	unknown	unknown	gnl\|CDD\|239245
NZ_CP036262.1\|WP_145349678.1\|425744_426524_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133022
NZ_CP036262.1\|WP_145349680.1\|426520_428119_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349673.1\|421410_421653_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|117819
NZ_CP036262.1\|WP_145349675.1\|421649_422270_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|222854
NZ_CP036262.1\|WP_145354854.1\|424682_425477_+\|Nif3-like-dinuclear-metal-center-hexameric-protein	unknown	unknown	gnl\|CDD\|376614
NZ_CP036262.1\|WP_145349661.1\|408706_408964_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349647.1\|404836_405295_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349655.1\|406699_406951_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349669.1\|416239_419101_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349671.1\|419097_419997_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238697
NZ_CP036262.1\|WP_145349649.1\|405571_405883_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354855.1\|428252_429587_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP036262.1\|WP_145349677.1\|423970_424501_+\|translation-initiation-factor-IF-3	unknown	unknown	gnl\|CDD\|234582
NZ_CP036262.1\|WP_145349653.1\|406204_406438_-\|addiction-module-protein	unknown	unknown	gnl\|CDD\|378247
NZ_CP036262.1\|WP_145349659.1\|407718_408039_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349663.1\|408960_409158_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349651.1\|405906_406212_-\|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	gnl\|CDD\|368240
NZ_CP036262.1\|WP_145354853.1\|415110_415299_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349665.1\|409830_411027_-\|tyrosine-type-recombinase/integrase	unknown	unknown	gnl\|CDD\|271193

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145349673.1\|421410_421653_-\|hypothetical-protein	gnl\|CDD\|117819	pfam09274, ParG, ParG. Members of this family of plasmid partition proteins adopt a ribbon-helix-helix fold, with a core of four alpha-helices. They are an essential component of the DNA partition complex of the multidrug resistance plasmid TP228.	6.0539e-06
NZ_CP036262.1\|WP_145349657.1\|407168_407501_-\|thioredoxin-family-protein	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	1.61585e-13
NZ_CP036262.1\|WP_145349671.1\|419097_419997_-\|hypothetical-protein	gnl\|CDD\|238697	cd01406, SIR2-like, Sir2-like: Prokaryotic group of uncharacterized Sir2-like proteins which lack certain key catalytic residues and conserved zinc binding cysteines; and are members of the SIR2 superfamily of proteins, silent information regulator 2 (Sir2) enzymes which catalyze NAD+-dependent protein/histone deacetylation.	8.51496e-17
NZ_CP036262.1\|WP_145349678.1\|425744_426524_+\|glycosyltransferase	gnl\|CDD\|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. DPM1 is the catalytic subunit of eukaryotic dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. In higher eukaryotes,the enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The 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. This protein family belongs to Glycosyltransferase 2 superfamily.	6.99108e-49
NZ_CP036262.1\|WP_145354855.1\|428252_429587_-\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	5.91934e-47
NZ_CP036262.1\|WP_145349677.1\|423970_424501_+\|translation-initiation-factor-IF-3	gnl\|CDD\|234582	PRK00028, infC, translation initiation factor IF-3; Reviewed.	1.11183e-70
NZ_CP036262.1\|WP_145349653.1\|406204_406438_-\|addiction-module-protein	gnl\|CDD\|378247	pfam09720, Unstab_antitox, Putative addiction module component. This entry defines several short bacterial proteins, typically about 75 amino acids long, which are always found as part of a pair (at least) of small genes. The other protein in the pair always belongs to a family of plasmid stabilisation proteins (IPR007712). It is likely that this protein and its partner comprise some form of addiction module - a pair of genes consisting of a stable toxin and an unstable antitoxin which mediate programmed cell death - although these gene-pairs are usually found on the bacterial main chromosome.	6.29126e-12
NZ_CP036262.1\|WP_145349675.1\|421649_422270_-\|AAA-family-ATPase	gnl\|CDD\|222854	PHA02518, PHA02518, ParA-like protein; Provisional.	4.54743e-58
NZ_CP036262.1\|WP_145354854.1\|424682_425477_+\|Nif3-like-dinuclear-metal-center-hexameric-protein	gnl\|CDD\|376614	pfam01784, NIF3, NIF3 (NGG1p interacting factor 3). This family contains several NIF3 (NGG1p interacting factor 3) protein homologs. NIF3 interacts with the yeast transcriptional coactivator NGG1p which is part of the ADA complex, the exact function of this interaction is unknown.	1.29187e-90
NZ_CP036262.1\|WP_145349651.1\|405906_406212_-\|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	gnl\|CDD\|368240	pfam05016, ParE_toxin, ParE toxin of type II toxin-antitoxin system, parDE. ParE is the toxin family of a type II toxin-antitoxin family. It is toxic towards DNA gyrase, but is neutralized by the antitoxin ParD. The family also encompasses RelE/ParE described in.	0.00621251
NZ_CP036262.1\|WP_145349665.1\|409830_411027_-\|tyrosine-type-recombinase/integrase	gnl\|CDD\|271193	cd01193, INT_IntI_C, Integron integrase and similar protiens, C-terminal catalytic domain. Integron integrases mediate site-specific DNA recombination between a proximal primary site (attI) and a secondary target site (attC) found within mobile gene cassettes encoding resistance or virulence factors. Unlike other site specific recombinases, the attC sites lack sequence conservation. Integron integrase exhibits broader DNA specificity by recognizing the non-conserved attC sites. The structure shows that DNA target site recognition are not dependent on canonical DNA but on the position of two flipped-out bases that interact in cis and in trans with the integrase. Integron-integrases are present in many natural occurring mobile elements, including transposons and conjugative plasmids. Vibrio, Shewanella, Xanthomonas, and Pseudomonas species harbor chromosomal super-integrons. All integron-integrases carry large inserts unlike the TnpF ermF-like proteins also seen in this group.	5.13599e-49

>NZ_CP036262.1|WP_145349665.1|409830_411027_-|tyrosine-type-recombinase/integrase
MKRWLVMSIRTFFDKFCYRDVTLGLATPRKPKRRPVVLSTREVARLLQAASTIRDKLVLGLMYATGMRVSEVVRVRFRDIDFDRNIIMTWQGKGRADRLVTLPQSYRELLRSMRAHGTAESYIFAGAAKGRFLSTRTVQRIMQTTMRIAKIDKPATPHSLRHSFATHSFEAGCDIRRIQKVLGHVHLETTTIYVHVAKPADPSQMPSPIDRLHAATGDGPSEPSHMATSSPALSRDPQNLPNVPSPPAEPVGRMQLFGKTSPDSSSTIQLTIRVPAEGRAIYFTGTTVTEARQGYLTLSVPPLEKWDKELNWLRPRQRERFQEADFYERLQQSIRSRFQAGTLITHRPEKQTTTATIATRIDRPHRDRSLPSTISKHISLSASTFPTAPFPTWSVRTK
>NZ_CP036262.1|WP_145349663.1|408960_409158_-|hypothetical-protein
MSLQELENTIAKLPPDELAKFREWFLDFDSAQFDKRIETDARDGRLDSLADAALRDHATGKSTPL
>NZ_CP036262.1|WP_145349661.1|408706_408964_-|hypothetical-protein
MNHFASPAFWECYKKLPDVIRTLADKNFALLKDNPDHPSLHFKKVGRYRSARVGRDFRALAVETDDGLLWFWIGNHAEYDRLIGA
>NZ_CP036262.1|WP_145349659.1|407718_408039_-|hypothetical-protein
MNLDADDARDYMKLLERAIIHLRYRIRYDDSVTVAEVHDILDSLHNIPAMLRGAGDWFTPDNIDADLERYDNKWLNADDGASRRRGLLELLQDVRNGDFSDDPPVA
>NZ_CP036262.1|WP_145349657.1|407168_407501_-|thioredoxin-family-protein
MSSPQLTHETYADFVASNSFAVVHCWAVWNGYDHKMRAALADQMPHFRQIAFAEFDVDPPDHHDICRELNVHGPPFLALYRDGALVTSRVGLMDRADLRAFLHGLLNPAA
>NZ_CP036262.1|WP_145349655.1|406699_406951_-|hypothetical-protein
MYARPDTIESTLWNFHWAWAIVRESEVRFRELRSETLSRHKAPSGLFSRFKHDNPDASDDEALAFTLDQWRAVSTELGVPLET
>NZ_CP036262.1|WP_145349653.1|406204_406438_-|addiction-module-protein
MNTQPQDLLSAALTLPEIERANIAGSLLRSLDPSPDPTADEAWAAEIKRRVESIDRGEVELTPWNDVMSAMRDRRNG
>NZ_CP036262.1|WP_145349651.1|405906_406212_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MDERPFWFHPDASAEVLVAHDRYGEVTFKLAERFQDELERSRQTITRGPQVWPEYLYGTQRYLLKGFPYFIVYRAVPDRIEIIAVAHERQRPGYWADRTVS
>NZ_CP036262.1|WP_145349649.1|405571_405883_+|hypothetical-protein
MSNRVTADQLIGADHHLRGGFEIELGHNPGDQFGIINGVHVKHLEAEPIARVLVILSSGFCHISGADNGRFLRHRPERSLNYWEFYQCQCQRPLPKSQGVPKA
>NZ_CP036262.1|WP_145349647.1|404836_405295_-|hypothetical-protein
MDERFLNYCDQLQPRLDALLAMPGIHPVAPPTGMPNRGVYLLTENDVHLYTGRSNTMPKRLRDHCTGGHRKAALAVKLTRLATGNPATYRRENSISVLMTQPDFATAFTDAQTRIRNMTLRYVEETDPVRQCLLEIYVSLVLRTTYNSWDTT
>NZ_CP036262.1|WP_145354853.1|415110_415299_-|hypothetical-protein
MHILKLAGIRYKSLNLVAVQRVETIAKRLFNFLVDTSKLLKLDVCIIEFAEAVRRQLHPSYE
>NZ_CP036262.1|WP_145349669.1|416239_419101_-|hypothetical-protein
MTTSFFSELANLKAILGGSTSTEEKWKEVKPLLADEPIKREFWSLLDSADWISVLESAAEFESPPTPDISEDASRFPRWDASKYLVRMASLAPADVARILASVRTANTSVNGDIIDAANKLPIDDAVCLVPAIRYAAENLSVWVHFKDACEFCVKLCDSGHMEEAFELAEALFLPREPASERSMHDPKDYWYREGLQQVSESLVSASPERMIICLRDWVGILGRVNRGEDSTSIADDYSYIWRPAIEEHEQNSDYDLAGFVVGVLREVCERAIGEDLIPVSRVLAILTEQELDVFRRFRVHLINVFADRVPELARAVLLDRASFDDFALKHEYARLVQDRFGELPESDRKSWIEFVDQGRPDVDREYPFFESDEHLTNYARYWRFHRLHLIRRHLSDQLLDEYNKLLEEFEDGKLAEFHSYSGPLRYGYESPIELDALRQLDFADALKAVCEWDGESTSSFGPSVQGLADRFEQYVKDNASSYSRFANELIDKPAPFVSAFLSAMRNAVTEGKAISIEPTLELCVWLIDGKRSAGGDSYVYEQERALDLIRGLLDAQTERKEPSQSLLDGRLAIWGCIETMCEATPNSWVLQDNEPDDPRDHDFTTLAINSARGKAVETAFAYAGWIRSLASEVTNQSFEALDLIEFRQVLESQACGKNRSWVGLAIIGSHLSTIYHFDERWLENHRDLIFRLEDVEEDPEEAFGWAAWNAFLTWTQPHRVYLDLFRSQYEYACSQTSEVAKTERRSQSPMRSLSQHIAIYYGRGYLSLEVNGSLIRILLTNARPCVRRQLLQFIGNSLRGEKELPQEVVNRFQSLWDFYWPMHGCNDFLTNPEEFVFADWFAFGSFDEVWALQKLKEAVFSVPAVIAGRDVVNRLAQQAERDPLSSIQLLQRFIESDDQNWRVAEWSAAATDILRTSLNSESSKARDIAESLIDRLGRSGFLEFGKLLGDKF
>NZ_CP036262.1|WP_145349671.1|419097_419997_-|hypothetical-protein
MANPTNALAYQPLLDSIENRDCIAVIGAGISSPDYPLWNALLTELLRDCGIRAEDLPAKIARDIASLADFARARNRAAYYDTLNRVFARRKSPECATRYHLLARIGFCSYINLNFDPVLCDVLNLHTNISVSTYPVLQPKHLRDGNVFHLHGRIDKDFPAEDGRIVLSKEDFKTAYHPIKSRVHAFLQSVFNDHDVCFLGCNPEEPNLKRILRSCESFQESLHGVTSPSRPRRFLLWNHDSAEPMLKKCGVNLVNYAKVDGAYTGLLDVLKHLAGDRPISHRQGGVESSTYASNDGGQP
>NZ_CP036262.1|WP_145349673.1|421410_421653_-|hypothetical-protein
MSKRITMSARPKPKPEVDNWVEMRESSIDVKPRTKPKRLTIDIDPELHTELKISCAKRGIQIADLLRNLIEGDVRRHDRG
>NZ_CP036262.1|WP_145349675.1|421649_422270_-|AAA-family-ATPase
MIYAFLNQKGGVGKTTLSIHTATELSSRGRRVLLVDADPQGSSLAWSNYREKSDFTVVGMAKATIHREVESLAQDYDDVIIDGPPRVTELARSIILAADVVVIPLQPSPMDVWAAAETVDLVREAQVFKPNIRCCLMLNRKIANTAIGRDVREALAELEVPILKSDIGQRVAFAETAANGATVLDQQRSKAAKEIKKFVNELRRIK
>NZ_CP036262.1|WP_145349677.1|423970_424501_+|translation-initiation-factor-IF-3
MALARRPPQTEQRDSTRINAQIRITPIRVIADDGEQLGIIPTEEALEKARESGLDLVEVAPTERPPVCRIMDYGKYKYEKNKKKNHGGTHNKTKEIRLRPKTGQEDINTRVRQAIKFLQHKDKVQVSVLFRGREMAHIEEGRKVMQSVIETLSEYGKVETTPQQHGRRMICMIAPR
>NZ_CP036262.1|WP_145354854.1|424682_425477_+|Nif3-like-dinuclear-metal-center-hexameric-protein
MEQFSRSLVSLAPLKLAESWDNVGLLVGDRKASVQRVMVCLTITPAVVAEAVSRQVDLVISHHPLPFKPLPRLTRDTIAGGMLLDLIQARVAVYSSHTAWDSASGGVNRQLADLLCLDSVVPLVPFESPADDATEPLGAGRCGRFVEPVTVRELAARIGEATASSRVRFVGNPEHRVAKVAFACGSGGSFLDAAARVGCDAMVTGEATFHTCLDAESRGIGLVMLGHYASERFAMESMAAQLAGLHPDLTIWPSENEADPIRQL
>NZ_CP036262.1|WP_145349678.1|425744_426524_+|glycosyltransferase
MSTVKPGESNERWLVALPVYNEAAYVDGVLDEVLAYAGDVLVVDDGSTDGTSEILQAREDVQVIRHPKNRGYGAALQTAFQYTIDEGYDGIVTLDCDGQHQPKRIPRFIEAAKTVDIVSGSRYLKQYEGDSQPPQQRLVINRQITKQINEQLGIDLTDAFCGFKAYRTEGLKKLRITDDGYAMPLQLWVEAAAAGLSVRELPVPLIYLDLERSFGGSLDHAETRLRYYNQVIEQSLAAVCADGRTIPAARSSLCQNSLG
>NZ_CP036262.1|WP_145349680.1|426520_428119_+|hypothetical-protein
MITLEVSTPFQAYQVPRADQTALVSPPLAEAPGLLKENQRLAAGWSFEFAGIPIAQLRQQARVDLLAAANQYTSAYRDYSGPQDPTSILLAGHQPQLFHPGVWFKNFALSKLGHSLSATPINLVVDNDLRGSGSVRVPAEGPDGRIQAASIAYDDPGASVPFEQHRIANRQLFNSFDERLAAAVAPWVDSPCVFEMWKHARKAAERCENTGCALASARHAVEGELGLQTLELPLSVACRSRSFAAFLIGLVGDLPRLHACYNDSVLEYRAAHGIRSQAHPVPLLGESDGWLEAPLWLYGDDAPERRQVWVKQQGDLLYLSDLQGVTVSIDYDPESPEMADQLYRLQSANFKLRPRALVTTMYSRLILGDLFLHGIGGGKYDQLGDRIMGRFFEITPPSFMVMSATVWLPRIGEAADSESVTRLQRMIRDTRFNPQRFFPGADRPEELLAEHRALLANVPTGAEKSEWHRRLMDVNTKLSAMLDSVRSRLAAQQREAQEHSRQWNVLASREIPFCAYPLEMLDETFTKLLSQH
>NZ_CP036262.1|WP_145354855.1|428252_429587_-|FtsX-like-permease-family-protein
MMWIRTLQLGVKSLLLHPLRSGLTMLGILIGVWAVIVLTAISQGASDQVQQQLESLGADTIILVSLKPPPEKLTSTSALKYGLTRDELEMIKANVPTLRSVVPIREIRRQFTRGDNTVDGRLVGCTPGYAQVNRLELRDRGGRFLTDADNSSSATVCVLSSGVADRLFPYEDPLGKRVYVPESTDYYQVVGVLKHRNASAAIGGSLDAQDFSNDIYVPLQTVRTRIGDRIVTRRSGQFQVEEMELNQITLRVNGGEEYVRSTAKMLESMIKPRHENLSDAAVVVPLELLEQARNLRLMFLGIGVMIACISLIVGGIGIMNIMLASVTERTREIGVRRALGAKRSDITRQFLVETVALSFAGAMLGIALGFLGPPMYNGFLGQVAYWAPDKFAALPEVIRDAKPKIVYATIPLAVIIAMSVGLASGLYPAIRAARMNPIDALRHE

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Crispr_ID: NZ_CP036262_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_4

658703-658795

Orphan

Consensus_repeat	Method
CTCATGCCGTCGCGTTCGCGACT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_4

>merge|NZ_CP036262|4|658703-658795|CRISPRCasFinder
CTCATGCCGTCGCGTTCGCGACTCTTAAGGTGCTAGGGGGCATGTTCCTGGGACTTGCGTCCCAGGCTTTCGCATGCCGTCGCGTTCGCGACT

>NZ_CP036262|4|4|658703-658795|CRISPRCasFinder
CTCATGCCGTCGCGTTCGCGACT	CTTAAGGTGCTAGGGGGCATGTTCCTGGGACTTGCGTCCCAGGCTTT
CGCATGCCGTCGCGTTCGCGACT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145349964.1\|648790_648985_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349980.1\|662998_664081_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	unknown	unknown	gnl\|CDD\|224182
NZ_CP036262.1\|WP_145349968.1\|649853_651116_-\|Bcr/CflA-family-efflux-MFS-transporter	unknown	unknown	gnl\|CDD\|340878
NZ_CP036262.1\|WP_145349963.1\|647446_648790_-\|Trk-system-potassium-transporter-TrkA	unknown	unknown	gnl\|CDD\|236541
NZ_CP036262.1\|WP_145349986.1\|668172_668490_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354876.1\|668012_668237_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|312856
NZ_CP036262.1\|WP_145349966.1\|648981_649620_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349978.1\|659899_661372_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293764
NZ_CP036262.1\|WP_145349988.1\|669127_669547_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|236715
NZ_CP036262.1\|WP_145354872.1\|652540_653485_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349972.1\|653549_655694_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|374209
NZ_CP036262.1\|WP_145349984.1\|665399_667919_-\|DUF1592-domain-containing-protein	unknown	unknown	gnl\|CDD\|377886
NZ_CP036262.1\|WP_145349982.1\|664080_665403_-\|DUF1552-domain-containing-protein	unknown	unknown	gnl\|CDD\|377875
NZ_CP036262.1\|WP_145349992.1\|670803_671487_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|372556
NZ_CP036262.1\|WP_145354874.1\|661586_662696_-\|DUF1593-domain-containing-protein	unknown	unknown	gnl\|CDD\|377887
NZ_CP036262.1\|WP_145349990.1\|670125_670434_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145349976.1\|657160_658603_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP036262.1\|WP_145349961.1\|643323_646704_-\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|274225
NZ_CP036262.1\|WP_145349970.1\|651304_652213_+\|N-acetylneuraminate-lyase	unknown	unknown	gnl\|CDD\|188641
NZ_CP036262.1\|WP_145349974.1\|656118_657111_+\|YHYH-protein	unknown	unknown	gnl\|CDD\|379520

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145349980.1\|662998_664081_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	gnl\|CDD\|224182	COG1262, COG1262, Uncharacterized conserved protein [Function unknown].	4.57756e-53
NZ_CP036262.1\|WP_145349982.1\|664080_665403_-\|DUF1552-domain-containing-protein	gnl\|CDD\|377875	pfam07586, HXXSHH, Protein of unknown function (DUF1552). A family of proteins identified in Rhodopirellula baltica.	2.08329e-103
NZ_CP036262.1\|WP_145349963.1\|647446_648790_-\|Trk-system-potassium-transporter-TrkA	gnl\|CDD\|236541	PRK09496, trkA, Trk system potassium transporter TrkA.	5.85208e-148
NZ_CP036262.1\|WP_145354876.1\|668012_668237_-\|hypothetical-protein	gnl\|CDD\|312856	pfam09492, Pec_lyase, Pectic acid lyase. Members of this family are isozymes of pectate lyase (EC:4.2.2.2), also called polygalacturonic transeliminase and alpha-1,4-D-endopolygalacturonic acid lyase.	5.6634e-10
NZ_CP036262.1\|WP_145349978.1\|659899_661372_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293764	cd16145, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036262.1\|WP_145349988.1\|669127_669547_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|236715	PRK10562, PRK10562, putative acetyltransferase; Provisional.	5.19566e-31
NZ_CP036262.1\|WP_145349970.1\|651304_652213_+\|N-acetylneuraminate-lyase	gnl\|CDD\|188641	cd00954, NAL, N-Acetylneuraminic acid aldolase, also called N-acetylneuraminate lyase (NAL). N-Acetylneuraminic acid aldolase, also called N-acetylneuraminate lyase (NAL), which catalyses the reversible aldol reaction of N-acetyl-D-mannosamine and pyruvate to give N-acetyl-D-neuraminic acid (D-sialic acid). It has a widespread application as biocatalyst for the synthesis of sialic acid and its derivatives. This enzyme has been shown to be quite specific for pyruvate as the donor, but flexible to a variety of D- and, to some extent, L-hexoses and pentoses as acceptor substrates. NAL is member of dihydrodipicolinate synthase family that comprises several pyruvate-dependent class I aldolases.	1.30436e-112
NZ_CP036262.1\|WP_145349972.1\|653549_655694_+\|hypothetical-protein	gnl\|CDD\|374209	pfam15902, Sortilin-Vps10, Sortilin, neurotensin receptor 3,. Sortilin, also known in mammals as neurotensin receptor-3, is the archetypical member of a Vps10-domain (Vps10-D) that binds neurotrophic factors and neuropeptides. This domain constitutes the entire luminal part of Sortilin and is activated in the trans-Golgi network by enzymatic propeptide cleavage. The structure of the domain has been determined as a ten-bladed propeller, with up to 9 BNR or beta-hairpin turns in it. The mature receptor binds various ligands, including its own propeptide (Sort-pro), neurotensin, the pro-forms of nerve growth factor-beta (NGF)6 and brain-derived neurotrophic factor (BDNF)7, lipoprotein lipase (LpL), apo lipoprotein AV14 and the receptor-associated protein (RAP)1.	4.61862e-09
NZ_CP036262.1\|WP_145349984.1\|665399_667919_-\|DUF1592-domain-containing-protein	gnl\|CDD\|377886	pfam07631, PSD4, Protein of unknown function (DUF1592). A region of similarity shared by several Rhodopirellula baltica cytochrome-like proteins that are predicted to be secreted. These proteins also match pfam07627, pfam07626, and pfam07624.	6.71793e-55
NZ_CP036262.1\|WP_145349992.1\|670803_671487_-\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|372556	pfam13313, DUF4082, Domain of unknown function (DUF4082). This family appears to be a parallel beta-helix repeated region that sits between successive Cadherin domains, pfam00028.	0.0012504
NZ_CP036262.1\|WP_145354874.1\|661586_662696_-\|DUF1593-domain-containing-protein	gnl\|CDD\|377887	pfam07632, DUF1593, Protein of unknown function (DUF1593). A family of proteins in Rhodopirellula baltica that are predicted to be secreted. Also, a member has been identified in Caulobacter crescentus. These proteins mat be related to pfam01156.	5.81606e-73
NZ_CP036262.1\|WP_145349976.1\|657160_658603_-\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	1.08607e-08
NZ_CP036262.1\|WP_145349961.1\|643323_646704_-\|c-type-cytochrome	gnl\|CDD\|274225	TIGR02604, Piru_Ver_Nterm, putative membrane-bound dehydrogenase domain. All proteins that score above the trusted cutoff score of 45 to this model are large proteins of either Pirellula sp. 1 or Verrucomicrobium spinosum. These proteins all contain, in addition to this domain, several hundred residues of highly variable sequence, and then a well-conserved C-terminal domain (TIGR02603) that features a putative cytochrome c-type heme binding motif CXXCH. The membrane-bound L-sorbosone dehydrogenase from Acetobacter liquefaciens (Gluconacetobacter liquefaciens) (SP\|Q44091) is homologous to this domain but lacks additional sequence regions shared by members of this family and belongs to a different clade of the larger family of homologs. It and its closely related homologs are excluded from the this model by scoring between the trusted (45) and noise (18) cutoffs.	1.37597e-56
NZ_CP036262.1\|WP_145349974.1\|656118_657111_+\|YHYH-protein	gnl\|CDD\|379520	pfam14240, YHYH, YHYH protein. This domain family is found in bacteria, eukaryotes and viruses, and is typically between 141 and 198 amino acids in length. There is a conserved YHYH sequence motif.	2.61805e-11
NZ_CP036262.1\|WP_145349968.1\|649853_651116_-\|Bcr/CflA-family-efflux-MFS-transporter	gnl\|CDD\|340878	cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.07206e-93

>NZ_CP036262.1|WP_145349976.1|657160_658603_-|IS4-family-transposase
MTARGFTCDEFGYLTSQTHQARKPPVCYQSFDSFRNRVHHARQCGDLYFASLLSKETIASAFGEATSILDAARVYNTSVTLWVFLSQVMSIHHGCVSAVTKLITYRVANRQRSCSAQTGAYCIARDKLDESAMHRLVTSSGQAIEAKAPNHWLWLGHRVITADGATVTMANTRDNQAEYPQLSSQAPGCGFPILRGVVLFALSTGVVLEMATGRYKGKLTHEVSLFRQIDQIIEETDVFLADRAYAGWFEMARVMQRDGHVVVRKHPMRRSDFRTGIRYGKDDHSIQIAKPLRPAWMSVEEYKTYPDFITIREIKIRIANTGFRTREIIVHTSLLDDTNYTKEDIATLFRRRWQAELNLRSLKTIMQMEHLRCKKPHRVRNEIRAHMLAYNLIRGVMAEVAIEGDVQPWQISFKSTLTTVSDMLPVLGLISNVDELCEVLYRCCLQHVVGNRPDRYEPRVLKRRPKIMQKPRHDYKPGEA
>NZ_CP036262.1|WP_145349974.1|656118_657111_+|YHYH-protein
MIHRFKPRLLTLSLMLGLLSFGSGCGPRGETIPQKVVQAVNPDHFVEESLVEPIRKEMRTLSDGSQAECYVITTKAVPPDHPLGPWAPKHVTDGEDKGGIWIKDGHVYNVSGEFVAHLDELYDDPEWNLVREDGSIKVTDTEEAFNLAARPNVDPRYENYAVECPPDVVEWKSYHNVYVIPVSPVYRSVTTDFHRVGDGHSPVGVAFNGVKYDPPAPIHMIIKAHTIAPFDHSGGHVNPHAGYHYHAATGKTKEIEQSDGHSPLIGYALDGFGIYAHLDTVGKEPEGLDECSGHYDDVRGYHYHAGAAGDNQIIGAFRGIAGSAEIVKPK
>NZ_CP036262.1|WP_145349972.1|653549_655694_+|hypothetical-protein
MSHLLAPKRIIAYHLRGVAAVCCLLFLLCLGIGQQSLAAAPPVWQPFGPGGGGWIEDVVSHPTNPQEVWAMTDLSGLFRSQDAGVTWRKMSSDVERGVVARKQIVSHNRQFAIDPTEPNRMYWGVCGMIWSSQDGGVSWQASYGNPPAPGNDKRTGVGHAMTVANDGTVFALDHESVLRTSRDHGATWSELTKPPVAQNSSDTPAFPFCLADGTLCVACRPSAGLAVSNDGGNSWSTKLATSIILNACAAPAGTGHDGTLYAFDSTGRLHRSEDSGKTFVVIKETRHQWKPGLRFAGGLAVSKSGKVMLWALGETVVSMDWGESWTRHRIETNWQRGSYAGMNRYASPEGKCSALAVTADGNVWLKCDSSLMCRSTDDGVSWTGSTEGLQVLCYFQGAAVSPHSPHQAMVAALDQGVFKTSDDGKSWQPMRIQPEWWDDKWQNHDGSVVKAHPTKPETWFAIIHGHGGTRHPRLHRTDDGGESWRLVLDVKKKFGGDWGRWLSDAEMGDLCFDPINPNIIYLSNYQLGVLRSEDGGATWVHTLKAKNGLNLVTSPSGQHVYLQCLKRNGLYASHDRGLTWGITYAADGVDGLAHHPTDESTLFVNDGQHENYWSYKGQRPSKLLKSTDAGKTWNELARLDGGPLYVDPVKPSVMLTSTLHGRGILRSTDGGMTWHEFHFDAPSHTTRGFTYGGLPGSVLYHMFGNMARTTQLYK
>NZ_CP036262.1|WP_145354872.1|652540_653485_+|hypothetical-protein
MHSTALLVPFLLFATAALAQHPQIPVGPNADLGGVLLMPAGDEWNRDVSKDPVDPRSDAIIAKIGAQTRLHEDFGLIWKGAPGGIPYYVVSGDQPKVPVAFAYAGESDPGPYPIPPNAPIEGGPEGAGDRHVIVLDKDNWRLYEMFHAFPIDGGKSWKASSGAIFDLKDLKPRPAGWTSADAAGLPILPGLARYDELCVKKKLTHALRFTVKKSRRAYVFPASHFASKHNDPDLPPMGMRVRLKADFDTSKFSGPARVLLEGLKTYGMILADNGGDWFVSGAPDDRWVHDELTPIRQVKGSDFEVVKMGPMTMR
>NZ_CP036262.1|WP_145349970.1|651304_652213_+|N-acetylneuraminate-lyase
MSQFKLSNLIAATYTPLNADGRLNLQQVGPLVEHLLGSGVTGLYVCGSTGEGMSLSCEDRRSVTDAFVTAAAGRVPVIVQVGHNSLDDAKQLAAHAQQVGADAISATCPSYFKVGTVGGLVDSMAEVASGAPELPFYYYHIPMLTGSKIDMVPFLTEGVARIPNLVGLKYTDTALHEFQECFELQDGRFDVVWGCDEMLLGALATGAQAAIGSTYNIAAPLYARLIEAFEKGDLQEARRLQGLSIQMIRTINLYPFHPAMKAVLKMKGIDVGGCRLPQGKLTAEEAKSLQSKLQSIGFFDWS
>NZ_CP036262.1|WP_145349968.1|649853_651116_-|Bcr/CflA-family-efflux-MFS-transporter
MPAKRSDLFIISLLGALSVVSPFAIDVYLPAFPELAAEFGVPSTTIALTLSSYFTGLALGQIIYGPLLDRFGRKKPLTFGLSLFVIASLGCAFAPNINALIGLRFIQGLGGCVAQVASIAMVRDFFPRNQAARVLSRLFLFIAVSPLLAPTIGSLIIQFAGWQSAFYALALIVAGILALVLTLLPEGHTPDPDIVLRPGPIFAEYWSIFRHPRFSTYAGAGAFSFAGLFTYVAGSPILFMDGFGVGGTTYSLIFAFLAAGFIGASQVNVLLLRRYSSEQLFRWFLTAQVAFALLFLAGSLAGILGLAGTLAMMLGFLGCIGITNPNAAALAIGPFSKNAGSASALLGFFQLGAGAIISTGISAASPEDQLPIIAIFGATSAIGLVILLQGQKRAFACPVEEEPSEVAEPGQDRLMPVETR
>NZ_CP036262.1|WP_145349966.1|648981_649620_-|hypothetical-protein
MSQTDPSKIEVDGIPIDLRNPAVAGILAWLFPGAGHFYQKRYAKGVLYMACILTTYVVGFIVGGAHVVYASWIPGDKRWHYVCQLGAGAIAMPALIEGYRMKNATQQFGDGVRSPLSYATDPDWKPLFGGLMAPPRRPVMEQSADEVSAWYARQGAGYEMGTWYTMIAGILNILVIYDACSGPLSTPISGRKKKAAKDEDETPSPNSTEKSS
>NZ_CP036262.1|WP_145349964.1|648790_648985_-|hypothetical-protein
MMSISPTYLLYYLPLLVSISLVYGATRHEDMTLILKHAAYTAYWITSFMGVIFLILLGIGYLVS
>NZ_CP036262.1|WP_145349963.1|647446_648790_-|Trk-system-potassium-transporter-TrkA
MHVMILGAGTVGTWVADILCRQGHSVTVVDQNAENVRRINAELDVRAVQGNASQSTVLFQCGVAASDICLALTGEDEVNIVAASMAKALGARRTVARVYAPAFRDLSTFDYQRHFGIDRLLSLEQLSATELARTIRNPGAIPLENFARGQLVVYEIEVAASAPAVGTKLSDLKLPSGVRVGSISRENRMWIASAGDEPRAGDQISLIGMPGDVADAHDLFDREKRFPRKQVIMIAGGGETGYHLAQSLGEHHFHVILLEKDAERCDYLSTQLKNITVLHASANRRMILEDEGAGKADWFVACTGNDENNIMACVEARELGAKHVLSVVGRADYANVVEKLGIDLAVSERDVAARQILGHLHEGSVISHSKLPNGSIGVYELEILENSEVSGKPLCDLPLSGNCLVAAIDRDGFVKVPKASDQLIPGDIVVALIDETVSQETLKLFQA
>NZ_CP036262.1|WP_145349961.1|643323_646704_-|c-type-cytochrome
MHVPPLFVLLASLFLSLAWCHSTTAQSEQAHANTSAAAEPAQPAASYGLGVRDTPWRSPAEEQAGFHLPAGFEINLFAAEPQIAKPLNMAFDKRGRLWVTQSSLYPYPSTNPDQEAEQTADAVVILEDTNGDGTADRKTTFADGLNIPIGVLPYGDGCLCFSIPNLWYLRDTDGDGRCDKREIVLGPFDTTRDTHGMVNALRDGNDGWIYACHGFNNQSTIAGTDGESITLISGNTFRFKADGSRVEQYTHGQVNPFGMTQDDWGYFYTADCHSKPITQLVKGAYYPSFGRPHDGLGFLPPMVDHLHGSTAISGIAYISPDSPIVPLRGQMISGNVMTSRLNRNAIEYRGATAVGIELPDFLTSDDPWFRPVDIQIGPQNQIVVADFYNRIIGHYEVPLEHPGRDRTSGRIWQIRYVGDSKTASTPTSDSAQDNKIARQQMANLQAAEGSNQIALLAREYLKDSNPHLARLAAERLGEHGDLNDVPALLKRLHQLDRADHVGRQSVRIAVASRLKDSSDQEKGYPWLDQLTATEKDALANILPAVDTSDAAALLLDYLAAAPVNKRTRNLFRQVAENATSDRLADCVQVAQRIAGEDWALQEEWLDLIWNTIDSGQSIPAPELRTWSGKLAKHRWAIHREERSLLSSHPPVFWHSDRGTHWPVQPRQNASGDSVRVSSSIPFGESYTGIQATGPFAAPDMIEFLIAGHRGPPAKPAHRLNEIRLVDADTNEVLEQAYPPRSDIAQKVRWDTHSLAGRMVQIEAIDGDSGNAYAWFAVGDFRPAWLNTFNTLETFQTDLQWMVRSASTDNNQAQLATLQAALEEPNYPPLFRLSIARAISQMQTSKDPRLVLEALLQAVLTHSADAVAPSSPWAIQWTTPASLPLILQNDSETMDKVCREITANQSTAGQTLFALRWVQEGGSTERILQMGDAGSLTAQVFANPEVWSALEPRLKDPQKAIAQALHTRGQSSESESNLAFMERMETIQGLQGDPLAGEPLFKQHCAACHQLRGTGTVLGPQLDGAIVRPQERLFEDILTPNRNVDKAFLTTSFLTLDGRVLVGLIQEESENQVRLIDGAGKVQTLSKKEIEFQKPTGRSLMPANFADLLQDQAFADLLAFLKEGDTK
>NZ_CP036262.1|WP_145349978.1|659899_661372_+|sulfatase-like-hydrolase/transferase
MNHVFTSIVFCLLFATNGLDVWAEPPSPQTTVAEDLPAASQKAHVKGDGGLSLTSQKPNIVLIMADDLGYGDLGCYGQKLISTPRIDQLAASGMRFTQAYAGAPVCTASRSVLMTGLHNGHTPARDNVPHYSTYFQEDDVTIAEVLKPAGYRCGGVGKWSLGDAGSVGRATHQGFDSWFGYLNQDHAHYYYPEYLDDDDGRFELTGNAASREHYSHDLLTDRALQFIRESQASPFFLYVAWTLPHFAAKDEDPDGLTVPTTAPYSDRDWDERSKKYAAMINMLDSDVGRILDLLSELELDENTLVIFTSDHGGHWSVPKPLKTNGALRGYKRDLTEGGIRVPFIARWTGTISANQTNQEVIAFQDMLPTFAELADVSPPQGIDGISVVDVMEGKKLDSTREFLYWDYGHCRARYDQAVRWKDWKGIRQGAGSDLQLYDLASDVSESHNIAANHPEIVRRIEAMMEGAVTPSERYPIGKRYRGGPLWTREK
>NZ_CP036262.1|WP_145354874.1|661586_662696_-|DUF1593-domain-containing-protein
MKSPHESGLYQSDGWDCPVINTILQEADADRNRIKELALKTNLNHLTALLTFLFVIAIHFAASVSASPPGGALSGDRPRVVISSDIGGSDPDDFQSLIHLLLYADVIDVEGLISSPPEAGRAKHILEVIDAYANDYSHLKSHSKAYPAADALRSVVKQGALDKASQKGWSEPTDGSRWIIQRAHAADKRPLWILVWGSITDVAQAIHDDPSIKSHIRVYSIGSWNTSQDSAARDYLFKNHTDLWWIESDTSFRGMYMGGLQDDDWGNLSFIQQNVKGHGSLGDLFFKKKHDIKMGDTPSFLYLLRGNPDDPTSPHWGGAFVATGHGKDYWTDNPDPSLSTSNRAGAKTVSNWRREYLEDWKYRMDRVNE
>NZ_CP036262.1|WP_145349980.1|662998_664081_-|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme
MKFPKLALPFIVVLLAPLTVSLAVSRATADDAGKPSKANALGMQMVRIPAGEYMRGFDNRNGRDHRFHLAHRYSTSQNFNAETPPQRVAISRSFEIGAREVTVAQFREFVEATDYQTDAERSDGGLGCFPDEKDYVDRFHKSAEITWQSPGFPQSDQHPVVVVSWNDAQAFCQWLSAKESATYRLPTEAEWEYACRGGTSTWYSWGQDPDEAYQHANVADAALEAAQPGTTRYQRAVKLDENQGDGVVFTAAVGSYRANAWGLHDMHGNVWEWCSDRWSGGLYESYFDGVPRQQRDDVLVRDPHFTEKTDQHKYGDWRVIRGGAWTCAPAAVRSSTRTYAEAADASVYTGFRIVRDTPQP
>NZ_CP036262.1|WP_145349982.1|664080_665403_-|DUF1552-domain-containing-protein
MNILKFQPLKRRTFLRGAGTCLTLPWLEAMLPRTARAATETPKAVPRMGMFYFGTGMNMRQFYPQGYGNDAKLSRILTPLEPHRGDFTVLSGTCLEKGGGHGGAYPFATSIAIGEKQSISPDQLAAKLHGKQTRFPSLQLSVKRGTGFGSQILATISWNGQGVPLAAENDPQAVFNQLFRPASEQQKAQQSDEFRQRRSVLDAVLSDAHQLTGKLGQADRHQLDQYFHSIREVEQTLSREIAWQDRPKPQPDLKGYGDYEHVVAPEGNGKFVYDTYGKLMYDLIALAYQTDSTRVVSYVVRTELAGGVYPEFGVNKGYHELTHHGNDPKNLEELAKVDTIYMQHWRYFLDRLASIRDGDGTLLDHTMLGFSSGMGIGHSKDQLPTVLSGGSGLGIRHQTHLKLNDNTPLSSLWQTMLEKMGVTVEGPFQDSRGTIGELVV
>NZ_CP036262.1|WP_145349984.1|665399_667919_-|DUF1592-domain-containing-protein
MLDRILFVAAALLCTPAAFATTFDDEIAPLLKQYCMDCHGPQEAQGKLRVDELTADFSRRDNAAAWIEVRNMIHLGEMPPADEPQLPAAAIEQVSVWIAAQLRAAEHAQRSTGGRVLMRRLNRREYTHSVADLLSMKFPVGESPLDVLPPEGTAEGFDKVSSALLLDPSLMTNYYRVARRIADRAIVDGPPEYPTETMRLEFEDIADSRAIRYLVRRLGMTPVPGGLELIEGNTRSFGLLNYPGQRGNNVAPTNGFYRFTLRAGGVPGADGQPPRLRVTQSHPDDAMEAIMEVDITAPIDQPQDYSVVVPRDTLGGELSVKLLNATGLHMSQRPGENFIRRNSELGKTGDFAEVLRINGRKVAEGWSGDRSTPDPDKLDVSTYPRAFLDYLEVEGPLYDQWPPQSHTKVLFRGDDATEDLEYARAIYARLLPLAWRRPIAPEETDPILQVVATELEQGESFHEAIRVGLATTLTSPKFLYIVEANHATAARTSPPRPLNDYELASRLSYFLWSSMPDAELFELARRNRLNDAATLSAQVDRMLADPKAERFVDGFARQWLRTDTFLSFTPAEYLYREYDEALSDAVVREPLEFFRTILQEQLSVRNFIDSDFVVINKRLARHYGIDGVNGDAFRRVPLPADSPRGGLLAMAGVHQAGSDGRRTKPIARAMYVREVLFNDPPDPPPPNVGEIEPNIRGQNLTVRERLIQHQQIDACAICHRSLDPYGLALENFNVIGAWRELQDGENFRGGDRPAIDPSGRLPNGAEFQSFVEFRAHLLEQDDRFRRALAEKLLIYALGRPIEPSDDATLSRATDTMARGDDTFHTLIKSLVTSKVFATK
>NZ_CP036262.1|WP_145354876.1|668012_668237_-|hypothetical-protein
MESCSANWQTLPTSRNRNAPLDKPSGCSDRDGDGGVKYDLQEIGSERRGGYTWYGTWGERVLASYARCPHRTGD
>NZ_CP036262.1|WP_145349986.1|668172_668490_-|hypothetical-protein
MQKGLYSKPTFDQFSGVHYLGWQEATRIEGCYRSVFNLDVSRDCKTWERKYRFETSQSFQSPTCHEHEGTIWLTISQSDHGGSSDRIMFGKLADLAHLPESERTP
>NZ_CP036262.1|WP_145349988.1|669127_669547_-|GNAT-family-N-acetyltransferase
MIRKYEASDLNDLLETWAAASELAHPFLTQEFLASERENIPNVYLPIADTWVFESEGQVIGFIALIGNEIGAIFVHPSIQRTGVGTSLMEKAKALHEELEVEVFVSNTIGRGFYAKCGFTLMEEKLHEPTGQQVMRLNC
>NZ_CP036262.1|WP_145349990.1|670125_670434_+|hypothetical-protein
MNQTTSIADGNILAVKSAAQDANAVQNAVNLIAIIGCFHRHLLALRQSGLNDDDLNNHPVSLAFVSKLNSLCRMKIEREMAAFSAIDRIAEGKSVEYEVLPL
>NZ_CP036262.1|WP_145349992.1|670803_671487_-|PEP-CTERM-sorting-domain-containing-protein
MMRTIQLAVACVTVLIATAGQVQAGVILDFAGGSTMFGAGDYTVGFTFSVTAPVAVDGLAWWDEGGDGLNSPHEVGLWTGGGSLLASTFVSNGSTIEPSTSGFGNWLITDIATLNLGLGDYVIGGVQPNSTGGDLLRFPATATTISGIVFGVPIQHFGNGLTLTMPNFTGTGTGTTGIIGALGPNLRLSTAAVPEPSSLALFGIGACVACVGTARRRRREQKQLATT

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Crispr_ID: NZ_CP036262_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_5

1030028-1030117

Orphan

Consensus_repeat	Method
TCTGTCGCCCTCCGGGCTAGCCAAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_5

>merge|NZ_CP036262|5|1030028-1030117|CRISPRCasFinder
TCTGTCGCCCTCCGGGCTAGCCAAGGCCTTAAAGACAGACCGGCGGCTGACGCCGCCGGCAAGTATCTGTCGCCCTCCGGGCTAGCCAAG

>NZ_CP036262|5|5|1030028-1030117|CRISPRCasFinder
TCTGTCGCCCTCCGGGCTAGCCAAG	GCCTTAAAGACAGACCGGCGGCTGACGCCGCCGGCAAGTA
TCTGTCGCCCTCCGGGCTAGCCAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145350313.1\|1046525_1047872_+\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145350301.1\|1036210_1037839_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|349772
NZ_CP036262.1\|WP_145350309.1\|1041812_1043576_+\|single-stranded-DNA-specific-exonuclease-RecJ	unknown	unknown	gnl\|CDD\|273193
NZ_CP036262.1\|WP_145350294.1\|1025259_1028151_+\|response-regulator	unknown	unknown	gnl\|CDD\|381085
NZ_CP036262.1\|WP_145350283.1\|1018477_1018921_-\|Na(+)/H(+)-antiporter-subunit-B	unknown	unknown	gnl\|CDD\|183563
NZ_CP036262.1\|WP_145350305.1\|1039170_1041393_+\|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl\|CDD\|377178
NZ_CP036262.1\|WP_145350311.1\|1045546_1046329_-\|SprT-family-zinc-dependent-metalloprotease	unknown	unknown	gnl\|CDD\|370932
NZ_CP036262.1\|WP_145354932.1\|1043820_1045293_+\|RtcB-family-protein	unknown	unknown	gnl\|CDD\|376465
NZ_CP036262.1\|WP_145350296.1\|1029476_1029809_+\|DUF971-domain-containing-protein	unknown	unknown	gnl\|CDD\|377616
NZ_CP036262.1\|WP_145354928.1\|1019507_1019837_-\|monovalent-cation/H(+)-antiporter-subunit-G	unknown	unknown	gnl\|CDD\|237169
NZ_CP036262.1\|WP_145350292.1\|1023024_1025049_-\|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl\|CDD\|238141
NZ_CP036262.1\|WP_145350285.1\|1018917_1019511_-\|DUF4040-domain-containing-protein	unknown	unknown	gnl\|CDD\|183561
NZ_CP036262.1\|WP_145350288.1\|1020138_1020624_-\|sodium:proton-antiporter	unknown	unknown	gnl\|CDD\|376653
NZ_CP036262.1\|WP_145350298.1\|1030547_1034249_-\|methionine-synthase	unknown	unknown	gnl\|CDD\|236539
NZ_CP036262.1\|WP_145350290.1\|1021678_1023022_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|225363
NZ_CP036262.1\|WP_145350307.1\|1041617_1041782_+\|50S-ribosomal-protein-L33	unknown	unknown	gnl\|CDD\|376336
NZ_CP036262.1\|WP_145350300.1\|1034639_1036142_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370676
NZ_CP036262.1\|WP_145350303.1\|1037913_1038741_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|132060
NZ_CP036262.1\|WP_145350286.1\|1019857_1020142_-\|pH-regulation-protein-F	unknown	unknown	gnl\|CDD\|237148
NZ_CP036262.1\|WP_145354930.1\|1028217_1029456_+\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|341239

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145350313.1\|1046525_1047872_+\|twin-arginine-translocation-signal-domain-containing-protein	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.45243e-27
NZ_CP036262.1\|WP_145350301.1\|1036210_1037839_+\|hypothetical-protein	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	5.25815e-22
NZ_CP036262.1\|WP_145350309.1\|1041812_1043576_+\|single-stranded-DNA-specific-exonuclease-RecJ	gnl\|CDD\|273193	TIGR00644, recJ, single-stranded-DNA-specific exonuclease RecJ. All proteins in this family are 5'-3' single-strand DNA exonucleases. These proteins are used in some aspects of mismatch repair, recombination, and recombinational repair. [DNA metabolism, DNA replication, recombination, and repair].	6.8603e-175
NZ_CP036262.1\|WP_145350294.1\|1025259_1028151_+\|response-regulator	gnl\|CDD\|381085	cd00156, REC, phosphoacceptor receiver (REC) domain of response regulators (RRs) and pseudo response regulators (PRRs). Two-component systems (TCSs) involving a sensor and a response regulator are used by bacteria to adapt to changing environments. Processes regulated by two-component systems in bacteria include sporulation, pathogenicity, virulence, chemotaxis, and membrane transport. Response regulators (RRs) share the common phosphoacceptor REC domain and different effector/output domains such as DNA, RNA, ligand-binding, protein-binding, or enzymatic domains. Response regulators regulate transcription, post-transcription or post-translation, or have functions such as methylesterases, adenylate or diguanylate cyclase, c-di-GMP-specific phosphodiesterases, histidine kinases, serine/threonine protein kinases, and protein phosphatases, depending on their output domains. The function of some output domains are still unknown. TCSs are found in all three domains of life - bacteria, archaea, and eukaryotes, however, the presence and abundance of particular RRs vary between the lineages. Archaea encode very few RRs with DNA-binding output domains; most are stand-alone REC domains. Among eukaryotes, TCSs are found primarily in protozoa, fungi, algae, and green plants. REC domains function as phosphorylation-mediated switches within RRs, but some also transfer phosphoryl groups in multistep phosphorelays.	3.94508e-06
NZ_CP036262.1\|WP_145350283.1\|1018477_1018921_-\|Na(+)/H(+)-antiporter-subunit-B	gnl\|CDD\|183563	PRK12508, PRK12508, Na(+)/H(+) antiporter subunit B.	6.12954e-58
NZ_CP036262.1\|WP_145350305.1\|1039170_1041393_+\|NADP-dependent-isocitrate-dehydrogenase	gnl\|CDD\|377178	pfam03971, IDH, Monomeric isocitrate dehydrogenase. NADP(+)-dependent isocitrate dehydrogenase (ICD) is an important enzyme of the intermediary metabolism, as it controls the carbon flux within the citric acid cycle and supplies the cell with 2-oxoglutarate EC:1.1.1.42 and NADPH for biosynthetic purposes.	0
NZ_CP036262.1\|WP_145350311.1\|1045546_1046329_-\|SprT-family-zinc-dependent-metalloprotease	gnl\|CDD\|370932	pfam10263, SprT-like, SprT-like family. This family represents a domain found in eukaryotes and prokaryotes. The domain contains a characteristic motif of the zinc metallopeptidases. This family includes the bacterial SprT protein.	0.000136406
NZ_CP036262.1\|WP_145354932.1\|1043820_1045293_+\|RtcB-family-protein	gnl\|CDD\|376465	pfam01139, RtcB, tRNA-splicing ligase RtcB. This family of RNA ligases (EC:6.5.1.3) join 2',3'-cyclic phosphate and 5'-OH ends. They catalyze the splicing of tRNA and may also participate in tRNA repair and recovery from stress-induced RNA damage.	5.25585e-126
NZ_CP036262.1\|WP_145350296.1\|1029476_1029809_+\|DUF971-domain-containing-protein	gnl\|CDD\|377616	pfam06155, DUF971, Protein of unknown function (DUF971). This family consists of several short bacterial proteins and one sequence from Oryza sativa. The function of this family is unknown.	2.14545e-21
NZ_CP036262.1\|WP_145354928.1\|1019507_1019837_-\|monovalent-cation/H(+)-antiporter-subunit-G	gnl\|CDD\|237169	PRK12674, PRK12674, putative monovalent cation/H+ antiporter subunit G; Reviewed.	4.00013e-24
NZ_CP036262.1\|WP_145350292.1\|1023024_1025049_-\|prolyl-oligopeptidase-family-serine-peptidase	gnl\|CDD\|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	1.10606e-12
NZ_CP036262.1\|WP_145350285.1\|1018917_1019511_-\|DUF4040-domain-containing-protein	gnl\|CDD\|183561	PRK12504, PRK12504, DUF4040 domain-containing protein.	1.16549e-63
NZ_CP036262.1\|WP_145350288.1\|1020138_1020624_-\|sodium:proton-antiporter	gnl\|CDD\|376653	pfam01899, MNHE, Na+/H+ ion antiporter subunit. Subunit of a Na+/H+ Prokaryotic antiporter complex.	2.69452e-29
NZ_CP036262.1\|WP_145350298.1\|1030547_1034249_-\|methionine-synthase	gnl\|CDD\|236539	PRK09490, metH, B12-dependent methionine synthase; Provisional.	0
NZ_CP036262.1\|WP_145350290.1\|1021678_1023022_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|225363	COG2804, PulE, Type II secretory pathway, ATPase PulE/Tfp pilus assembly pathway, ATPase PilB [Cell motility and secretion / Intracellular trafficking and secretion].	6.71658e-45
NZ_CP036262.1\|WP_145350307.1\|1041617_1041782_+\|50S-ribosomal-protein-L33	gnl\|CDD\|376336	pfam00471, Ribosomal_L33, Ribosomal protein L33.	1.19874e-07
NZ_CP036262.1\|WP_145350300.1\|1034639_1036142_+\|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.	4.86406e-06
NZ_CP036262.1\|WP_145350303.1\|1037913_1038741_+\|AAA-family-ATPase	gnl\|CDD\|132060	TIGR03015, pepcterm_ATPase, putative secretion ATPase, PEP-CTERM locus subfamily. Members of this protein are marked as probable ATPases by the nucleotide binding P-loop motif GXXGXGKTT, a motif DEAQ similar to the DEAD/H box of helicases, and extensive homology to ATPases of MSHA-type pilus systems and to GspA proteins associated with type II protein secretion systems. [Protein fate, Protein and peptide secretion and trafficking].	5.6215e-48
NZ_CP036262.1\|WP_145350286.1\|1019857_1020142_-\|pH-regulation-protein-F	gnl\|CDD\|237148	PRK12599, PRK12599, putative monovalent cation/H+ antiporter subunit F; Reviewed.	4.99126e-13
NZ_CP036262.1\|WP_145354930.1\|1028217_1029456_+\|AMP-binding-protein	gnl\|CDD\|341239	cd05913, PaaK, Phenylacetate-CoA ligase (also known as PaaK). PaaK catalyzes the first step in the aromatic degradation pathway, by converting phenylacetic acid (PA) into phenylacetyl-CoA (PA-CoA). Phenylacetate-CoA ligase has been found in proteobacteria as well as gram positive prokaryotes. The enzyme is specifically induced after aerobic growth in a chemically defined medium containing PA or phenylalanine (Phe) as the sole carbon source. PaaKs are members of the adenylate-forming enzyme (AFE) family. However, sequence comparison reveals divergent features of PaaK with respect to the superfamily, including a novel N-terminal sequence.	1.06564e-123

>NZ_CP036262.1|WP_145350296.1|1029476_1029809_+|DUF971-domain-containing-protein
MSNSGIVHPTSIERLGSDQIAILWSDGSRTEPTIQQLRRACPCATCREKKKAADKPPEPSKPIGLPVLKAEEAQSLQITAMRPAGQYAYNIQFSDGHHSGLFPFELLRSI
>NZ_CP036262.1|WP_145354930.1|1028217_1029456_+|AMP-binding-protein
MGPSALADLQLCKLNRLLADVLPHSEFYQAKYGRQDWQLESLDELKSIPFLKKGELVNPQPGHPARFHCLPRRQYVRFHQTSGTTGRPMPVWDTAADWEWWIRTWQYVLDAAEVTPDDTVAMAFSFGPFIGFWSANDALIRRQALVVPAGGMSTRARLQLIIHSQATLLCCTPTYALHLAEVAREDNLDLRSSSVTRIIVAGEPGGSIPEVRQQIELVWDARVIDHSGASELGPWGVGATDGSGLFVIESEFIAESLVPGTDQPAADGELGELILTGLGRVGGPAIRFRTGDLVRATRQHDHDCRFLFLPGGVLGRADDMLVIRGVNVFPSGVESVVRSIDGLGEFRMIATRVAAMDQLEVEVEGDTAAATELGKVLQVRLGLRIPVRSVPHQSLPRSEAKSRRLDDRRFLP
>NZ_CP036262.1|WP_145350294.1|1025259_1028151_+|response-regulator
MTRRFHCLILAGWMFCLLLGGAPSQNVMAQPPAADPFAPVDPFAPAGDNPGMDPNNPFGGPVEGNLFDPAAAPAAAAGQALGEILQPTDPFIEELRRYAAGSNAKLALAIRQAARIGNWKEVEDFLQILAGRKPSQAVLSSMANTIDGPLLARMRLQPKLSPESIKMIDQMRSAAQASASDNKILRQAILALKSPSVDLQLKGYRALFTGGDNAIAELVTAAVQPSPVVPREKLVPVLREMGPSAEHAIRQFVLYGAPELRAGALETLVLWDRKAALGDLVTALHAADATDKERSIAASTLAQDYKPLPSGKEAEQFLTGKLNDAVRLAKRTARDEKMKTIWVIGEDGKTITPQLATARLAAVQQAAVAAARLRPLSGLSLEAQRAALITDIDYAVQQDLLFGTDPKDFDSLRESYSADAFSLPQLQSLLSDSMDQRRDAATVGILRLLPADPQLVRSMSQDQTPLVDAASHPDPRVRYEASLLIGRTKMDEPYRGSSVVLRRWLEMAALKNRPTALVVQPRPAAAMRLEAMLIQQGYNVEIVPSVQEAALRVARGGDIQVIVATTDLPDLPPIELVDRIRRISLGANIPILFYGDDRAGTSNNSLSAPVRRIVPPRRTLDQDRYDVLLESLQLLNDDLEFVLFQPPIDVPVNRPDPQLEQRENYAAALEKVRAAVLKSKLDRNLSFFGLALGIDAHPIALTLQPETEGGIAQAEILRTSLEDLGFEFESVSDLAALQTRLEDRRPVHMVFLSASSAPEYARDLVNQIRETKEGAKVPIFFYGGSDDGLETARFESQLRRRHAISTPESFTSVMDAVNAAAALPPLDSDERKAYEIGSMSILSAVAQDPKQEFYDLRTNEIDKVLGAPSSGSNESHLAVLAGLGTAESQDALAELAANESVAQPVRMRAAERFAESVQRFGTRLSRDHVALQYQRYNRTNNEDIRASIGIVLDAMEKRVSSTN
>NZ_CP036262.1|WP_145350292.1|1023024_1025049_-|prolyl-oligopeptidase-family-serine-peptidase
MTVLFQSRCRLFALTLLVLGILGGFATIQAAEPVVAPDSETTAKRFDWKGTESKWEGFKRFDFQVDQHKAYVVAPETVAPGAPWVWRARFPGFHAEADKILLDRGFHVAHIDTANQLGSPRAMKTWDAFYQAMVSQGLAKQVALEGVSRGGLFVYAFAAQWPDRVACIYCDTPVCDMKSWPGGKGKGVGSASTWKTCLAEYGFSEAEALAYQGNPIDRLETIAAAKIPILHIVSLTDRVVPPEENTFILADRYRKLGGQMDIIEVAEGTEKSQGHHFTHPDPVRVADFIEAHATVLPNTNDYFELRGSLDNSRIQFERNKKGRVAFMGGSITEMKGWRERTQAYLRSRFPETEFEFIDAGISSTGSTPGSFRLMRDVLAAGDIDLFFEEAAVNDKHNFRQPTEIVRGMEGILRHARRANPKMDIVVMQFVDPYHMTDYRNGQTPKVIEQHQRVAKHYDVPTIQLAKEVTERIDANQFTWKEDFRDLHPSDYGHRLYASTIRRLLSTAWEPPLRDTATAVDHNMPQPIDPFSYDRGTMVPLESATDLQGFRIDPKCDPRANDIGGGVRKRFHDVPMLVGTSAGDSFALKFSGRGVGIFVAAGPDAGKISYQVDGGETKHLDLFTKWSGGLHIPWVHVLESELPEGEHVLRIQIDADHNEASKGTACRIVNLLVNE
>NZ_CP036262.1|WP_145350290.1|1021678_1023022_+|general-secretion-pathway-protein-GspE
MPPKDPQEEPQLWQSVPPIEFSVVVGTREQQQGLEILARQAPGYPVAAGQIAHALKVRATHIMMDFTQQATAMRYQIDGQWENLPPLPRDAGDAMLYTLKQVSGLNPADRRSAQLGKCATKVKKAKFTITVQSQGTKTGERVLVRIEPDKAPFAGLTDLGMRDKMREITKAALDADGALVLISAPKGTGLTTTWQVSMEAADRLTRDFQSVENEDRKEPETINISANYYGPKTGKTAGELVRSMILKEPDVFVLPEIPDDEVLASILDQVANNEKAAYTRLVAQDAVEAAVKLVAKHRSCAKAIASTLKAVTSQRLVRRLCENCRQPFEPSPQLLKQLGIPQGRVGVLYRAYVPPPIEQQVDEKGNPAPVPVCHVCNGRSYLGRAGVFELLQPGPQFRAALLKTQDVNKLRQVAKAEGHRGLQTEAVLTVARGITSLEEVKRVFAGG
>NZ_CP036262.1|WP_145350288.1|1020138_1020624_-|sodium:proton-antiporter
MKYTLTLSAALAANWLLWSGYFNHPFLLGVGAVSCIFCVYIARRMKIVDDEGAPVQLGIRPFTRYAPWLIKEIVVANLDVTRILLARKMPIQRCVVEVDAPQKTELGRVILANSITLTPGTVAINLHGSQITVHALSLADAEEDIAGEMSDRICDLEPPQS
>NZ_CP036262.1|WP_145350286.1|1019857_1020142_-|pH-regulation-protein-F
MTMTHLFLATSIAILVTMTLALIRAMLGPTVFDRVLALNMFGTKTVLLICVLDFMSGRDDFLDLALLYSLMNFIGMVALLRFTEFGDFGGENLE
>NZ_CP036262.1|WP_145354928.1|1019507_1019837_-|monovalent-cation/H(+)-antiporter-subunit-G
MTGNILCWLFLVSGAFFSLIGGIGILRLPEFFSRMHGGGITDTLGAGLILTGLMFYAGFSLVTVKLITILFFVWITSPTSCHALARSALAHGLKPELDASILQKKGDKS
>NZ_CP036262.1|WP_145350285.1|1018917_1019511_-|DUF4040-domain-containing-protein
MIAIDIIILALLAATAVTIARIRDLWAAVMFTGIYSFLSASWMLNLDAPDVAFTEAAVGAGISTVLMLSTLALTGFKQGRSGVRIVPLLAVVATGGILIYGTLDMHHFGDPNAPVQIYPKESFVQKSQPDMHGLPNVVTALLASYRGYDTLGETAVIFTAGTAVLLILRREKPRSSRPGSPESDSPESEQNTEGASA
>NZ_CP036262.1|WP_145350283.1|1018477_1018921_-|Na(+)/H(+)-antiporter-subunit-B
MIQTTFPIVRIVTKLLIPYILLFGLYVQFHGDFGPGGGFQAGVIFASGLILYGLVFGLEAIQRVAPPALMERLTALGVLIYGGTGVLTMYLGGQFLDYSTLEHSVGHGILPSGQHLGILLVEMGVGITVTSVMTMIFYAFAGRRRSV
>NZ_CP036262.1|WP_145350298.1|1030547_1034249_-|methionine-synthase
MLQASNSESILPELVRERILILDGAMGTMIQRLNLDEKAVRGERFAEHHKDLNRFSDILCLTHPDKITDIHRAYFAAGADIVETNSFGASPVGMIEFDLPLELVEEINIAAVTCAKKAADEFTEKNPSRPRFVAGSIGPTSRQTAISTNVDDAAHRDVTFHEMADSYHRQIVALAGAGVDILLPETAIDTLNLKALLFAIQQYYDGGGRRIPVMASGTFDRGGRTFVSGQSVEAFVTAIRHFPLLSIGMNCALGPDIMRPHLEELAKVSPVPVSCHPNAGLPNEMGAYDLGPKAMGEMIADFASNQWLNIVGGCCGTTPDHIREIDAAVKNIRPRQDADQPVYTRLSGQLPFAMRPEVPFTMIGERTNVTGSRAFARLIRGDKYDEAVEVAREQVLNGAAVIDLNFDDGLLDGVEAMTRFLRLIAGDEVVAAVPLMIDSSKWEVIEAGLQNVQGKAIVNSISLKDGEEKFLERARLIRQYGAATVVMAFDEQGQAAEKDHKVAICKRAYDLLVNEVQFPPEDIIFDPNILTVATGMSEHNNYAIDFIEAVREIKKVCPGVKTSGGVSNISFSFRGNDPVREAMHSAFLYHAVKAGLDMGIVNAGQLEVYEEIPKDLLEHVEDVLLNRREDATDRMLDFAETVKGSGKKKSAEDLSWRERDVSERLKHALLKGVDKFVVEDAEEARQQLPRCLDVIEGPLMAGMQVVGDLFGEGKMFLPQVVKSARVMKKAVAYLEPFMEEEKRLNGTAMHSHRGKFLIATVKGDVHDIGKNIVGVVLQCNNYEVIDLGVMVSAERILEEAKKQEVDLVGLSGLITPSLDEMAHVASEMKRLGMSTPLLIGGATTSAKHTAVRIAPRYDFPVVHVLDASRGVGVVEKLLNKDNRDAFIKENNKQQEQLVASFRDRRQTLIPYEEALAKKFETDWESVRIDTPEFLGTKTLTDYPLEELRKYIDWSPFFMTWELKGKYPKIFESDKYGAQARELYDDGNRLLDQMIANNSLRACGVYGFFPVASDGDSVILYTDDQRTEERTRFHFLRQQWERKGQDDYRSLADYIAPVDSGRKDYLGAFAVTAGLGADELAETYRAKQDDYTAIMVQAVADRLAEAFAELLHEKARNEWAFGKEENFSKDDLIAESYRGIRPAAGYPACPDHTEKSTLFELLDAENQAHVQLTESYAMTPGASVSGLYFAHPQAKYFTVDRITRDQVQDYAKRKGWKLRDMERWLAPNLAYDPD
>NZ_CP036262.1|WP_145350300.1|1034639_1036142_+|hypothetical-protein
MTHPGNPAKSGHPGFQSSNLSHDSVGSDDPPVLFRLPALNQAASAAPASPKSRLTEDTGSPANSFPPPPPVAAAGSNSFPPPPVQPAVPNQASPAPTANTAERESRNAHTPDTNQPAGRSWTENMGTRLAVIALVLAAAGVMLLISRNGEDKSLQIAEDETDQLLADLGIPANGDAGNDAAPEFSTTETPDPAIDFDFTPTKPPATAPPAERGDVDLAASPAQRAPAELPAWDIDTAATETSGPLGSGDPAARTADARADDSRADFATDSAPSAISEPATINEPSGDEGFELTAPRSPYDSQTRSSMRAPETNRFATAPEFQPSAATQPAAPSNVAPQPQDRVASLPQANVAQRVSSDTLGQPSSRSAPQPSQTETPYAVSDWSQYLPAESNPAAAANVAQQPGSPQQQPVVAQQQPGYPQQQPGFSQQQPGYPQQPGGYGQQAAGGYGEVPHVAQAPQGYGPAPAAGATQPGQYPSSPYGGAGGMIESSDVPVSPYDNR
>NZ_CP036262.1|WP_145350301.1|1036210_1037839_+|hypothetical-protein
MSKIDQAFVKAFAKERPRTAPPTPESIAAEMVAMGMSSFWVDPSNNDLLRKDEPQSIGQTSTGRRRGSRSVKSAPPVSPPAQAASPSASDEPSKAAPDASVSKRIRPDQATASTESHSIELLRFDRAQMEISPEKLLRARLDASSFPAFTVAHDSLEDIVPERISAADATLPVDTTEEATTHVDDARFVPTTWGDHAPAPATPQIDHPEVASSASAPAPAAPETVSAPLPAAGPLRFDSPHPSRPATEVNSNAYQTAVEEVAEIQFAPASEEADVTRREMPAVEKAVPVQEAVSPNAFAQQAMEQASPVQSLPFQEAPLPVEQSSASAPKTSGAFEAAWEVDGFDAPSIVRELMVAGDMVNNAGQPLAQAAAEGMQAVLVSSPRRGDGRSTLAMALALSAAATGCRVALVDGDWEKPSLADDFQLELEFGWPEAIRGGVPLSETAVHGVEDGVTLFPIVPAENAPQPSADALRQTVDSLRPHFDLILVDGPTADTPLQYSGFQSAIVIHNRQSYDSVGLNHCIQQLRYAGIAHVGVAENFSA
>NZ_CP036262.1|WP_145350303.1|1037913_1038741_+|AAA-family-ATPase
MYESYWNLNERPFENWSDPRFYYPSEIHQTALLKVRYAVENRRAAVAICGDSGIGKSLIVDALAAQLPDPFAPVAKLAFPQLAGSELLGYVTDELTGTTGPNDETSRTSLRRLDDFFADNVDAGRHAVLIVDEAHLLTAPEQLETLRLLLNLQREQAQAEAAWTLVLVGHATLLSVIERNRALDERMSVKCMLSRMNSEQTAAYIQHRLQAAGCENHPIFSAEAIETLYVRSGGIPRRINRLADLALMVGYAEELEQIDAAHIDGVHQELVTIAA
>NZ_CP036262.1|WP_145350305.1|1039170_1041393_+|NADP-dependent-isocitrate-dehydrogenase
MSQTSEIVYTLTDEAPALATRSLLPIIQAFTRSSGVSVRLKDISLACRILAQFSDVLPADQQRSDVLAELGELAKTPDANIIKLPNVSASIPQLNTAIAELQSHGYAIPDYPADPQNDAERETKSRYAKVLGSAVNPVLREGNSDRRVAAPVKKYAQDHPHSMGEWSSDSKTRVASMAQGDFYGSEQSHVMVHAGEIRIELESPTGEITVLKPSLELLPGEVIDASCMSRKALRSYLEEQIAQAGRDQALLSLHLKATMMKVSDPIIFGHAVTVFFAPVFEKYAETLESLGVNPNNGLGDLLRKIESLPEAEKVAIQADIEAVYAQQPRLAMVDSDKGITNLHVPSDVIIDASMPAAIRSSGKMWGPDGKLHDTTALIPDRCYAGVYQATIDFCKKHGAFDVTTMGSVSNVGLMAQKAEEYGSHDKTFEIPHAGTVRAIDQDGNVLTEHVVEEGDIWRMCQTKDAPIRDWVNLAVKRARATGNAAIFWLDANRAHDANLIAKVRHYLDELETDGLEIEILSPIVAAKETCQRSRDGLDTISVTGNVLRDYLTDLFPILELGTSAKMLSIVPLLAGGGLFETGAGGSAPKHVQQFVSENHLRWDSLGEFLALAVSLEDLGQKTGNEKLLALAKGLDQANGAYLSHNRSPSRKAGEIDNRGGHFYLALYWAQAIAGSSDNAELRSEFGALAKELAANEQTIVDELNAVQGAPVDLGGYFNPDEKKVEAAMRPSATLNRILPG
>NZ_CP036262.1|WP_145350307.1|1041617_1041782_+|50S-ribosomal-protein-L33
MAKSKKKVETVFLICEETGDYNYTLRRKPGGEKLRLKKYCPRVRKHTWHVEKKK
>NZ_CP036262.1|WP_145350309.1|1041812_1043576_+|single-stranded-DNA-specific-exonuclease-RecJ
MRKEWRVLPLDQGRVEQLARLARIPDVVAQLLVSRGVYDLTAAKQFLDAKLSDLRDPLDLPGVPLAVEVIAKAIRSKAPIVIYGDYDADGMTSAAILFRGLKLMGSDVSYYVPNRLEEGYGLSSAALEKLAQRGKKLVISVDCGVGSVDEAKLCKTLGMQLVITDHHRIDGELPDAAAIVHPRLPGTSYPFGELCGAGVAFKLAWALCQEICESKRVTNQLRQYLLEALALAAIGTVADVVPLVDENRILVKHGLKSLRAHPGPGVAQLMRITKIDQRSDLQSEDIAFSIAPRLNAAGRLGQAQLGVELLTIQEETRAIQLAEYLDQLNANRVSLERSVYLAAQKQATDDYDPEADSALVLAGSGWHLGVIGVVAGRLAEKYGRPVLILSLDPVNGRPATGSGRAGGPHIDLHEALGECEHRLQKFGGHRAAAGLTLEDAQVDDFRSDFCEAVAKQVAESDHVAEVKIDAEAGIGQLSYQSVRQIEQLAPFGQGNPRPVLYARGVQLAEPSRRMGGGDRHLTLRVTQDGVSIRGVAFGQGDWCEELNAHEGPFDIAYRPVINEFRGQRNVEIQLVDWRPTHAAVVGS
>NZ_CP036262.1|WP_145354932.1|1043820_1045293_+|RtcB-family-protein
MIPTGEATAILPAGNHHSPVKVFGNEKIRATFDDLCLQQAINSRCAPGVTEVVLNPDAHCGYGAPIGCVLASPTHIYPGPVGFDIKCSMSLLQTDVPADAMIDKTIRRELIHAVCRRIPTGMGKGARDVPKSRRVEEKTGVAAMTDGASSDVLAALGVPVAWADRCEDAFHRGHDGSADALRQRLYYLRQGKTFSRFRSTVQQLGSYGGGNHFGECEVVDVVDDNESRQIANVFGLRDQHVAFLSHCGSRGIGHRLASGQFKQLEHKFDQWKIPYPGNDKQLVYAPIGSSEANDYIDDMSLGANFATVNHLLINALVLEAFQEIIPGTTGNLVYFISHNIARQEIVDNRETWVHRKGATRAFPAGHHALKRTPFEHTGHPILLPGNPQAGSSVMVGLPGAKESCYSVNHGAGRALGRRRAIRELDQKQIDASFDSADILSNCRRYPRDEAPAAYKDFEEVLRSVKQAGLAKEVARLRARFVIKDSSDADD
>NZ_CP036262.1|WP_145350311.1|1045546_1046329_-|SprT-family-zinc-dependent-metalloprotease
MNEKERSKLGEMVLSLPAKNKDTVARQHQIYSDSLRISRAMDRPNFTRVANDDLRQMAKMYDELFFEGRLLKLAADEGLKFGWSSRMTKNAGKTVTLYPHNYKRGDRRKFEIILSSALLFQTFSDIDRPVEVTGIVCRDRLQAMQRVLEHELVHLVEMLVWDDSSCSKSLFQRIANRAFGHTQHQHDLITQRERAARKFKIGVGSKVNFQFEGQPLQGVVNRITRRATVLVPDQAGALFDDGKRYRKYYVPLEHLRKRSA
>NZ_CP036262.1|WP_145350313.1|1046525_1047872_+|twin-arginine-translocation-signal-domain-containing-protein
MAHTDEKSSHPSPQRSAAPRREFLKGAAALGGAAAALSVTAPKLHAAGSDVIRIALIGCGGRGRGAALNAMAADPKVRLVALADLFDQSITDCRKQLTKQKPDQVELSDETCFVGFDAYKKAIELADVVLLASPPHYRPDHLEAAVAADKHIFCEKPIATDATGVRRVLAICEEADKKNLNIVSGLCWRYDQGVRETMGQIFDGKIGRVIGSQANYLTGPVWIRPRKDGESEMAYQCRNWYYFNWLSGDHITEQFIHSLDKALWLRHDEPPVKAYGMGGRGLRSDLTQGDIFDHFAVVYEWADGSTTNAFTRQVRGAYNQVEDFVYGSDGKASVLANKIEGKNSWKFDGKDKVNMYQQEHNELFEAVQGKRPRINNGTYMCRSTLLAILGREVCYSGKEITWDEAINSPQDLRPQKYSFDAEAPAVKVPKPGVYKFPIAKPGDKSGSV

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Crispr_ID: NZ_CP036262_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_6

1030190-1030374

Orphan

Consensus_repeat	Method
CGCTAAGAAGGGACGCCGCGAGCCCTCCGGCCCGAGTGTAGGGATGCGCAA	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP036262_6

>merge|NZ_CP036262|6|1030190-1030374|PILER-CR
CGCGAGCCCTCCGGCCCGAGCGTAGGGATGCGAAACAGGCCGGACGGCTCGCGCCGTTCCGCTAAGAGTGGGCGCCGCGAGCCCTCCGGCCCGAGTGTAGGGATGCGCAACAGGCCGGACGGCTCGCGCCGTTCCGCTAAGAAGGGACGCCGCGAGCCCTCCGGCCCGAGTGTAGGGATGCGCAA

>NZ_CP036262|6|1|1030190-1030374|PILER-CR
CGCGAGCCCTCCGGCCCGAGCGTAGGGATGCGAAACAGGCCGGACGGCTCG	CGCCGTTCCGCTAAGAGTGGGCGCCGC
GAGCCCTCCGGCCCGAGTGTAGGGATGCGCAACAGGCCGGACGGCTCGCGC	CGTTCCGCTAAGAAGGGACGCCGC
GAGCCCTCCGGCCCGAGTGTAGGGATGCGCAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145350313.1\|1046525_1047872_+\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145350301.1\|1036210_1037839_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|349772
NZ_CP036262.1\|WP_145350309.1\|1041812_1043576_+\|single-stranded-DNA-specific-exonuclease-RecJ	unknown	unknown	gnl\|CDD\|273193
NZ_CP036262.1\|WP_145350294.1\|1025259_1028151_+\|response-regulator	unknown	unknown	gnl\|CDD\|381085
NZ_CP036262.1\|WP_145350283.1\|1018477_1018921_-\|Na(+)/H(+)-antiporter-subunit-B	unknown	unknown	gnl\|CDD\|183563
NZ_CP036262.1\|WP_145350305.1\|1039170_1041393_+\|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl\|CDD\|377178
NZ_CP036262.1\|WP_145350311.1\|1045546_1046329_-\|SprT-family-zinc-dependent-metalloprotease	unknown	unknown	gnl\|CDD\|370932
NZ_CP036262.1\|WP_145354932.1\|1043820_1045293_+\|RtcB-family-protein	unknown	unknown	gnl\|CDD\|376465
NZ_CP036262.1\|WP_145350296.1\|1029476_1029809_+\|DUF971-domain-containing-protein	unknown	unknown	gnl\|CDD\|377616
NZ_CP036262.1\|WP_145354928.1\|1019507_1019837_-\|monovalent-cation/H(+)-antiporter-subunit-G	unknown	unknown	gnl\|CDD\|237169
NZ_CP036262.1\|WP_145350292.1\|1023024_1025049_-\|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl\|CDD\|238141
NZ_CP036262.1\|WP_145350285.1\|1018917_1019511_-\|DUF4040-domain-containing-protein	unknown	unknown	gnl\|CDD\|183561
NZ_CP036262.1\|WP_145350288.1\|1020138_1020624_-\|sodium:proton-antiporter	unknown	unknown	gnl\|CDD\|376653
NZ_CP036262.1\|WP_145350298.1\|1030547_1034249_-\|methionine-synthase	unknown	unknown	gnl\|CDD\|236539
NZ_CP036262.1\|WP_145350290.1\|1021678_1023022_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|225363
NZ_CP036262.1\|WP_145350307.1\|1041617_1041782_+\|50S-ribosomal-protein-L33	unknown	unknown	gnl\|CDD\|376336
NZ_CP036262.1\|WP_145350300.1\|1034639_1036142_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370676
NZ_CP036262.1\|WP_145350303.1\|1037913_1038741_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|132060
NZ_CP036262.1\|WP_145350286.1\|1019857_1020142_-\|pH-regulation-protein-F	unknown	unknown	gnl\|CDD\|237148
NZ_CP036262.1\|WP_145354930.1\|1028217_1029456_+\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|341239

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145350313.1\|1046525_1047872_+\|twin-arginine-translocation-signal-domain-containing-protein	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.45243e-27
NZ_CP036262.1\|WP_145350301.1\|1036210_1037839_+\|hypothetical-protein	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	5.25815e-22
NZ_CP036262.1\|WP_145350309.1\|1041812_1043576_+\|single-stranded-DNA-specific-exonuclease-RecJ	gnl\|CDD\|273193	TIGR00644, recJ, single-stranded-DNA-specific exonuclease RecJ. All proteins in this family are 5'-3' single-strand DNA exonucleases. These proteins are used in some aspects of mismatch repair, recombination, and recombinational repair. [DNA metabolism, DNA replication, recombination, and repair].	6.8603e-175
NZ_CP036262.1\|WP_145350294.1\|1025259_1028151_+\|response-regulator	gnl\|CDD\|381085	cd00156, REC, phosphoacceptor receiver (REC) domain of response regulators (RRs) and pseudo response regulators (PRRs). Two-component systems (TCSs) involving a sensor and a response regulator are used by bacteria to adapt to changing environments. Processes regulated by two-component systems in bacteria include sporulation, pathogenicity, virulence, chemotaxis, and membrane transport. Response regulators (RRs) share the common phosphoacceptor REC domain and different effector/output domains such as DNA, RNA, ligand-binding, protein-binding, or enzymatic domains. Response regulators regulate transcription, post-transcription or post-translation, or have functions such as methylesterases, adenylate or diguanylate cyclase, c-di-GMP-specific phosphodiesterases, histidine kinases, serine/threonine protein kinases, and protein phosphatases, depending on their output domains. The function of some output domains are still unknown. TCSs are found in all three domains of life - bacteria, archaea, and eukaryotes, however, the presence and abundance of particular RRs vary between the lineages. Archaea encode very few RRs with DNA-binding output domains; most are stand-alone REC domains. Among eukaryotes, TCSs are found primarily in protozoa, fungi, algae, and green plants. REC domains function as phosphorylation-mediated switches within RRs, but some also transfer phosphoryl groups in multistep phosphorelays.	3.94508e-06
NZ_CP036262.1\|WP_145350283.1\|1018477_1018921_-\|Na(+)/H(+)-antiporter-subunit-B	gnl\|CDD\|183563	PRK12508, PRK12508, Na(+)/H(+) antiporter subunit B.	6.12954e-58
NZ_CP036262.1\|WP_145350305.1\|1039170_1041393_+\|NADP-dependent-isocitrate-dehydrogenase	gnl\|CDD\|377178	pfam03971, IDH, Monomeric isocitrate dehydrogenase. NADP(+)-dependent isocitrate dehydrogenase (ICD) is an important enzyme of the intermediary metabolism, as it controls the carbon flux within the citric acid cycle and supplies the cell with 2-oxoglutarate EC:1.1.1.42 and NADPH for biosynthetic purposes.	0
NZ_CP036262.1\|WP_145350311.1\|1045546_1046329_-\|SprT-family-zinc-dependent-metalloprotease	gnl\|CDD\|370932	pfam10263, SprT-like, SprT-like family. This family represents a domain found in eukaryotes and prokaryotes. The domain contains a characteristic motif of the zinc metallopeptidases. This family includes the bacterial SprT protein.	0.000136406
NZ_CP036262.1\|WP_145354932.1\|1043820_1045293_+\|RtcB-family-protein	gnl\|CDD\|376465	pfam01139, RtcB, tRNA-splicing ligase RtcB. This family of RNA ligases (EC:6.5.1.3) join 2',3'-cyclic phosphate and 5'-OH ends. They catalyze the splicing of tRNA and may also participate in tRNA repair and recovery from stress-induced RNA damage.	5.25585e-126
NZ_CP036262.1\|WP_145350296.1\|1029476_1029809_+\|DUF971-domain-containing-protein	gnl\|CDD\|377616	pfam06155, DUF971, Protein of unknown function (DUF971). This family consists of several short bacterial proteins and one sequence from Oryza sativa. The function of this family is unknown.	2.14545e-21
NZ_CP036262.1\|WP_145354928.1\|1019507_1019837_-\|monovalent-cation/H(+)-antiporter-subunit-G	gnl\|CDD\|237169	PRK12674, PRK12674, putative monovalent cation/H+ antiporter subunit G; Reviewed.	4.00013e-24
NZ_CP036262.1\|WP_145350292.1\|1023024_1025049_-\|prolyl-oligopeptidase-family-serine-peptidase	gnl\|CDD\|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	1.10606e-12
NZ_CP036262.1\|WP_145350285.1\|1018917_1019511_-\|DUF4040-domain-containing-protein	gnl\|CDD\|183561	PRK12504, PRK12504, DUF4040 domain-containing protein.	1.16549e-63
NZ_CP036262.1\|WP_145350288.1\|1020138_1020624_-\|sodium:proton-antiporter	gnl\|CDD\|376653	pfam01899, MNHE, Na+/H+ ion antiporter subunit. Subunit of a Na+/H+ Prokaryotic antiporter complex.	2.69452e-29
NZ_CP036262.1\|WP_145350298.1\|1030547_1034249_-\|methionine-synthase	gnl\|CDD\|236539	PRK09490, metH, B12-dependent methionine synthase; Provisional.	0
NZ_CP036262.1\|WP_145350290.1\|1021678_1023022_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|225363	COG2804, PulE, Type II secretory pathway, ATPase PulE/Tfp pilus assembly pathway, ATPase PilB [Cell motility and secretion / Intracellular trafficking and secretion].	6.71658e-45
NZ_CP036262.1\|WP_145350307.1\|1041617_1041782_+\|50S-ribosomal-protein-L33	gnl\|CDD\|376336	pfam00471, Ribosomal_L33, Ribosomal protein L33.	1.19874e-07
NZ_CP036262.1\|WP_145350300.1\|1034639_1036142_+\|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.	4.86406e-06
NZ_CP036262.1\|WP_145350303.1\|1037913_1038741_+\|AAA-family-ATPase	gnl\|CDD\|132060	TIGR03015, pepcterm_ATPase, putative secretion ATPase, PEP-CTERM locus subfamily. Members of this protein are marked as probable ATPases by the nucleotide binding P-loop motif GXXGXGKTT, a motif DEAQ similar to the DEAD/H box of helicases, and extensive homology to ATPases of MSHA-type pilus systems and to GspA proteins associated with type II protein secretion systems. [Protein fate, Protein and peptide secretion and trafficking].	5.6215e-48
NZ_CP036262.1\|WP_145350286.1\|1019857_1020142_-\|pH-regulation-protein-F	gnl\|CDD\|237148	PRK12599, PRK12599, putative monovalent cation/H+ antiporter subunit F; Reviewed.	4.99126e-13
NZ_CP036262.1\|WP_145354930.1\|1028217_1029456_+\|AMP-binding-protein	gnl\|CDD\|341239	cd05913, PaaK, Phenylacetate-CoA ligase (also known as PaaK). PaaK catalyzes the first step in the aromatic degradation pathway, by converting phenylacetic acid (PA) into phenylacetyl-CoA (PA-CoA). Phenylacetate-CoA ligase has been found in proteobacteria as well as gram positive prokaryotes. The enzyme is specifically induced after aerobic growth in a chemically defined medium containing PA or phenylalanine (Phe) as the sole carbon source. PaaKs are members of the adenylate-forming enzyme (AFE) family. However, sequence comparison reveals divergent features of PaaK with respect to the superfamily, including a novel N-terminal sequence.	1.06564e-123

>NZ_CP036262.1|WP_145350296.1|1029476_1029809_+|DUF971-domain-containing-protein
MSNSGIVHPTSIERLGSDQIAILWSDGSRTEPTIQQLRRACPCATCREKKKAADKPPEPSKPIGLPVLKAEEAQSLQITAMRPAGQYAYNIQFSDGHHSGLFPFELLRSI
>NZ_CP036262.1|WP_145354930.1|1028217_1029456_+|AMP-binding-protein
MGPSALADLQLCKLNRLLADVLPHSEFYQAKYGRQDWQLESLDELKSIPFLKKGELVNPQPGHPARFHCLPRRQYVRFHQTSGTTGRPMPVWDTAADWEWWIRTWQYVLDAAEVTPDDTVAMAFSFGPFIGFWSANDALIRRQALVVPAGGMSTRARLQLIIHSQATLLCCTPTYALHLAEVAREDNLDLRSSSVTRIIVAGEPGGSIPEVRQQIELVWDARVIDHSGASELGPWGVGATDGSGLFVIESEFIAESLVPGTDQPAADGELGELILTGLGRVGGPAIRFRTGDLVRATRQHDHDCRFLFLPGGVLGRADDMLVIRGVNVFPSGVESVVRSIDGLGEFRMIATRVAAMDQLEVEVEGDTAAATELGKVLQVRLGLRIPVRSVPHQSLPRSEAKSRRLDDRRFLP
>NZ_CP036262.1|WP_145350294.1|1025259_1028151_+|response-regulator
MTRRFHCLILAGWMFCLLLGGAPSQNVMAQPPAADPFAPVDPFAPAGDNPGMDPNNPFGGPVEGNLFDPAAAPAAAAGQALGEILQPTDPFIEELRRYAAGSNAKLALAIRQAARIGNWKEVEDFLQILAGRKPSQAVLSSMANTIDGPLLARMRLQPKLSPESIKMIDQMRSAAQASASDNKILRQAILALKSPSVDLQLKGYRALFTGGDNAIAELVTAAVQPSPVVPREKLVPVLREMGPSAEHAIRQFVLYGAPELRAGALETLVLWDRKAALGDLVTALHAADATDKERSIAASTLAQDYKPLPSGKEAEQFLTGKLNDAVRLAKRTARDEKMKTIWVIGEDGKTITPQLATARLAAVQQAAVAAARLRPLSGLSLEAQRAALITDIDYAVQQDLLFGTDPKDFDSLRESYSADAFSLPQLQSLLSDSMDQRRDAATVGILRLLPADPQLVRSMSQDQTPLVDAASHPDPRVRYEASLLIGRTKMDEPYRGSSVVLRRWLEMAALKNRPTALVVQPRPAAAMRLEAMLIQQGYNVEIVPSVQEAALRVARGGDIQVIVATTDLPDLPPIELVDRIRRISLGANIPILFYGDDRAGTSNNSLSAPVRRIVPPRRTLDQDRYDVLLESLQLLNDDLEFVLFQPPIDVPVNRPDPQLEQRENYAAALEKVRAAVLKSKLDRNLSFFGLALGIDAHPIALTLQPETEGGIAQAEILRTSLEDLGFEFESVSDLAALQTRLEDRRPVHMVFLSASSAPEYARDLVNQIRETKEGAKVPIFFYGGSDDGLETARFESQLRRRHAISTPESFTSVMDAVNAAAALPPLDSDERKAYEIGSMSILSAVAQDPKQEFYDLRTNEIDKVLGAPSSGSNESHLAVLAGLGTAESQDALAELAANESVAQPVRMRAAERFAESVQRFGTRLSRDHVALQYQRYNRTNNEDIRASIGIVLDAMEKRVSSTN
>NZ_CP036262.1|WP_145350292.1|1023024_1025049_-|prolyl-oligopeptidase-family-serine-peptidase
MTVLFQSRCRLFALTLLVLGILGGFATIQAAEPVVAPDSETTAKRFDWKGTESKWEGFKRFDFQVDQHKAYVVAPETVAPGAPWVWRARFPGFHAEADKILLDRGFHVAHIDTANQLGSPRAMKTWDAFYQAMVSQGLAKQVALEGVSRGGLFVYAFAAQWPDRVACIYCDTPVCDMKSWPGGKGKGVGSASTWKTCLAEYGFSEAEALAYQGNPIDRLETIAAAKIPILHIVSLTDRVVPPEENTFILADRYRKLGGQMDIIEVAEGTEKSQGHHFTHPDPVRVADFIEAHATVLPNTNDYFELRGSLDNSRIQFERNKKGRVAFMGGSITEMKGWRERTQAYLRSRFPETEFEFIDAGISSTGSTPGSFRLMRDVLAAGDIDLFFEEAAVNDKHNFRQPTEIVRGMEGILRHARRANPKMDIVVMQFVDPYHMTDYRNGQTPKVIEQHQRVAKHYDVPTIQLAKEVTERIDANQFTWKEDFRDLHPSDYGHRLYASTIRRLLSTAWEPPLRDTATAVDHNMPQPIDPFSYDRGTMVPLESATDLQGFRIDPKCDPRANDIGGGVRKRFHDVPMLVGTSAGDSFALKFSGRGVGIFVAAGPDAGKISYQVDGGETKHLDLFTKWSGGLHIPWVHVLESELPEGEHVLRIQIDADHNEASKGTACRIVNLLVNE
>NZ_CP036262.1|WP_145350290.1|1021678_1023022_+|general-secretion-pathway-protein-GspE
MPPKDPQEEPQLWQSVPPIEFSVVVGTREQQQGLEILARQAPGYPVAAGQIAHALKVRATHIMMDFTQQATAMRYQIDGQWENLPPLPRDAGDAMLYTLKQVSGLNPADRRSAQLGKCATKVKKAKFTITVQSQGTKTGERVLVRIEPDKAPFAGLTDLGMRDKMREITKAALDADGALVLISAPKGTGLTTTWQVSMEAADRLTRDFQSVENEDRKEPETINISANYYGPKTGKTAGELVRSMILKEPDVFVLPEIPDDEVLASILDQVANNEKAAYTRLVAQDAVEAAVKLVAKHRSCAKAIASTLKAVTSQRLVRRLCENCRQPFEPSPQLLKQLGIPQGRVGVLYRAYVPPPIEQQVDEKGNPAPVPVCHVCNGRSYLGRAGVFELLQPGPQFRAALLKTQDVNKLRQVAKAEGHRGLQTEAVLTVARGITSLEEVKRVFAGG
>NZ_CP036262.1|WP_145350288.1|1020138_1020624_-|sodium:proton-antiporter
MKYTLTLSAALAANWLLWSGYFNHPFLLGVGAVSCIFCVYIARRMKIVDDEGAPVQLGIRPFTRYAPWLIKEIVVANLDVTRILLARKMPIQRCVVEVDAPQKTELGRVILANSITLTPGTVAINLHGSQITVHALSLADAEEDIAGEMSDRICDLEPPQS
>NZ_CP036262.1|WP_145350286.1|1019857_1020142_-|pH-regulation-protein-F
MTMTHLFLATSIAILVTMTLALIRAMLGPTVFDRVLALNMFGTKTVLLICVLDFMSGRDDFLDLALLYSLMNFIGMVALLRFTEFGDFGGENLE
>NZ_CP036262.1|WP_145354928.1|1019507_1019837_-|monovalent-cation/H(+)-antiporter-subunit-G
MTGNILCWLFLVSGAFFSLIGGIGILRLPEFFSRMHGGGITDTLGAGLILTGLMFYAGFSLVTVKLITILFFVWITSPTSCHALARSALAHGLKPELDASILQKKGDKS
>NZ_CP036262.1|WP_145350285.1|1018917_1019511_-|DUF4040-domain-containing-protein
MIAIDIIILALLAATAVTIARIRDLWAAVMFTGIYSFLSASWMLNLDAPDVAFTEAAVGAGISTVLMLSTLALTGFKQGRSGVRIVPLLAVVATGGILIYGTLDMHHFGDPNAPVQIYPKESFVQKSQPDMHGLPNVVTALLASYRGYDTLGETAVIFTAGTAVLLILRREKPRSSRPGSPESDSPESEQNTEGASA
>NZ_CP036262.1|WP_145350283.1|1018477_1018921_-|Na(+)/H(+)-antiporter-subunit-B
MIQTTFPIVRIVTKLLIPYILLFGLYVQFHGDFGPGGGFQAGVIFASGLILYGLVFGLEAIQRVAPPALMERLTALGVLIYGGTGVLTMYLGGQFLDYSTLEHSVGHGILPSGQHLGILLVEMGVGITVTSVMTMIFYAFAGRRRSV
>NZ_CP036262.1|WP_145350298.1|1030547_1034249_-|methionine-synthase
MLQASNSESILPELVRERILILDGAMGTMIQRLNLDEKAVRGERFAEHHKDLNRFSDILCLTHPDKITDIHRAYFAAGADIVETNSFGASPVGMIEFDLPLELVEEINIAAVTCAKKAADEFTEKNPSRPRFVAGSIGPTSRQTAISTNVDDAAHRDVTFHEMADSYHRQIVALAGAGVDILLPETAIDTLNLKALLFAIQQYYDGGGRRIPVMASGTFDRGGRTFVSGQSVEAFVTAIRHFPLLSIGMNCALGPDIMRPHLEELAKVSPVPVSCHPNAGLPNEMGAYDLGPKAMGEMIADFASNQWLNIVGGCCGTTPDHIREIDAAVKNIRPRQDADQPVYTRLSGQLPFAMRPEVPFTMIGERTNVTGSRAFARLIRGDKYDEAVEVAREQVLNGAAVIDLNFDDGLLDGVEAMTRFLRLIAGDEVVAAVPLMIDSSKWEVIEAGLQNVQGKAIVNSISLKDGEEKFLERARLIRQYGAATVVMAFDEQGQAAEKDHKVAICKRAYDLLVNEVQFPPEDIIFDPNILTVATGMSEHNNYAIDFIEAVREIKKVCPGVKTSGGVSNISFSFRGNDPVREAMHSAFLYHAVKAGLDMGIVNAGQLEVYEEIPKDLLEHVEDVLLNRREDATDRMLDFAETVKGSGKKKSAEDLSWRERDVSERLKHALLKGVDKFVVEDAEEARQQLPRCLDVIEGPLMAGMQVVGDLFGEGKMFLPQVVKSARVMKKAVAYLEPFMEEEKRLNGTAMHSHRGKFLIATVKGDVHDIGKNIVGVVLQCNNYEVIDLGVMVSAERILEEAKKQEVDLVGLSGLITPSLDEMAHVASEMKRLGMSTPLLIGGATTSAKHTAVRIAPRYDFPVVHVLDASRGVGVVEKLLNKDNRDAFIKENNKQQEQLVASFRDRRQTLIPYEEALAKKFETDWESVRIDTPEFLGTKTLTDYPLEELRKYIDWSPFFMTWELKGKYPKIFESDKYGAQARELYDDGNRLLDQMIANNSLRACGVYGFFPVASDGDSVILYTDDQRTEERTRFHFLRQQWERKGQDDYRSLADYIAPVDSGRKDYLGAFAVTAGLGADELAETYRAKQDDYTAIMVQAVADRLAEAFAELLHEKARNEWAFGKEENFSKDDLIAESYRGIRPAAGYPACPDHTEKSTLFELLDAENQAHVQLTESYAMTPGASVSGLYFAHPQAKYFTVDRITRDQVQDYAKRKGWKLRDMERWLAPNLAYDPD
>NZ_CP036262.1|WP_145350300.1|1034639_1036142_+|hypothetical-protein
MTHPGNPAKSGHPGFQSSNLSHDSVGSDDPPVLFRLPALNQAASAAPASPKSRLTEDTGSPANSFPPPPPVAAAGSNSFPPPPVQPAVPNQASPAPTANTAERESRNAHTPDTNQPAGRSWTENMGTRLAVIALVLAAAGVMLLISRNGEDKSLQIAEDETDQLLADLGIPANGDAGNDAAPEFSTTETPDPAIDFDFTPTKPPATAPPAERGDVDLAASPAQRAPAELPAWDIDTAATETSGPLGSGDPAARTADARADDSRADFATDSAPSAISEPATINEPSGDEGFELTAPRSPYDSQTRSSMRAPETNRFATAPEFQPSAATQPAAPSNVAPQPQDRVASLPQANVAQRVSSDTLGQPSSRSAPQPSQTETPYAVSDWSQYLPAESNPAAAANVAQQPGSPQQQPVVAQQQPGYPQQQPGFSQQQPGYPQQPGGYGQQAAGGYGEVPHVAQAPQGYGPAPAAGATQPGQYPSSPYGGAGGMIESSDVPVSPYDNR
>NZ_CP036262.1|WP_145350301.1|1036210_1037839_+|hypothetical-protein
MSKIDQAFVKAFAKERPRTAPPTPESIAAEMVAMGMSSFWVDPSNNDLLRKDEPQSIGQTSTGRRRGSRSVKSAPPVSPPAQAASPSASDEPSKAAPDASVSKRIRPDQATASTESHSIELLRFDRAQMEISPEKLLRARLDASSFPAFTVAHDSLEDIVPERISAADATLPVDTTEEATTHVDDARFVPTTWGDHAPAPATPQIDHPEVASSASAPAPAAPETVSAPLPAAGPLRFDSPHPSRPATEVNSNAYQTAVEEVAEIQFAPASEEADVTRREMPAVEKAVPVQEAVSPNAFAQQAMEQASPVQSLPFQEAPLPVEQSSASAPKTSGAFEAAWEVDGFDAPSIVRELMVAGDMVNNAGQPLAQAAAEGMQAVLVSSPRRGDGRSTLAMALALSAAATGCRVALVDGDWEKPSLADDFQLELEFGWPEAIRGGVPLSETAVHGVEDGVTLFPIVPAENAPQPSADALRQTVDSLRPHFDLILVDGPTADTPLQYSGFQSAIVIHNRQSYDSVGLNHCIQQLRYAGIAHVGVAENFSA
>NZ_CP036262.1|WP_145350303.1|1037913_1038741_+|AAA-family-ATPase
MYESYWNLNERPFENWSDPRFYYPSEIHQTALLKVRYAVENRRAAVAICGDSGIGKSLIVDALAAQLPDPFAPVAKLAFPQLAGSELLGYVTDELTGTTGPNDETSRTSLRRLDDFFADNVDAGRHAVLIVDEAHLLTAPEQLETLRLLLNLQREQAQAEAAWTLVLVGHATLLSVIERNRALDERMSVKCMLSRMNSEQTAAYIQHRLQAAGCENHPIFSAEAIETLYVRSGGIPRRINRLADLALMVGYAEELEQIDAAHIDGVHQELVTIAA
>NZ_CP036262.1|WP_145350305.1|1039170_1041393_+|NADP-dependent-isocitrate-dehydrogenase
MSQTSEIVYTLTDEAPALATRSLLPIIQAFTRSSGVSVRLKDISLACRILAQFSDVLPADQQRSDVLAELGELAKTPDANIIKLPNVSASIPQLNTAIAELQSHGYAIPDYPADPQNDAERETKSRYAKVLGSAVNPVLREGNSDRRVAAPVKKYAQDHPHSMGEWSSDSKTRVASMAQGDFYGSEQSHVMVHAGEIRIELESPTGEITVLKPSLELLPGEVIDASCMSRKALRSYLEEQIAQAGRDQALLSLHLKATMMKVSDPIIFGHAVTVFFAPVFEKYAETLESLGVNPNNGLGDLLRKIESLPEAEKVAIQADIEAVYAQQPRLAMVDSDKGITNLHVPSDVIIDASMPAAIRSSGKMWGPDGKLHDTTALIPDRCYAGVYQATIDFCKKHGAFDVTTMGSVSNVGLMAQKAEEYGSHDKTFEIPHAGTVRAIDQDGNVLTEHVVEEGDIWRMCQTKDAPIRDWVNLAVKRARATGNAAIFWLDANRAHDANLIAKVRHYLDELETDGLEIEILSPIVAAKETCQRSRDGLDTISVTGNVLRDYLTDLFPILELGTSAKMLSIVPLLAGGGLFETGAGGSAPKHVQQFVSENHLRWDSLGEFLALAVSLEDLGQKTGNEKLLALAKGLDQANGAYLSHNRSPSRKAGEIDNRGGHFYLALYWAQAIAGSSDNAELRSEFGALAKELAANEQTIVDELNAVQGAPVDLGGYFNPDEKKVEAAMRPSATLNRILPG
>NZ_CP036262.1|WP_145350307.1|1041617_1041782_+|50S-ribosomal-protein-L33
MAKSKKKVETVFLICEETGDYNYTLRRKPGGEKLRLKKYCPRVRKHTWHVEKKK
>NZ_CP036262.1|WP_145350309.1|1041812_1043576_+|single-stranded-DNA-specific-exonuclease-RecJ
MRKEWRVLPLDQGRVEQLARLARIPDVVAQLLVSRGVYDLTAAKQFLDAKLSDLRDPLDLPGVPLAVEVIAKAIRSKAPIVIYGDYDADGMTSAAILFRGLKLMGSDVSYYVPNRLEEGYGLSSAALEKLAQRGKKLVISVDCGVGSVDEAKLCKTLGMQLVITDHHRIDGELPDAAAIVHPRLPGTSYPFGELCGAGVAFKLAWALCQEICESKRVTNQLRQYLLEALALAAIGTVADVVPLVDENRILVKHGLKSLRAHPGPGVAQLMRITKIDQRSDLQSEDIAFSIAPRLNAAGRLGQAQLGVELLTIQEETRAIQLAEYLDQLNANRVSLERSVYLAAQKQATDDYDPEADSALVLAGSGWHLGVIGVVAGRLAEKYGRPVLILSLDPVNGRPATGSGRAGGPHIDLHEALGECEHRLQKFGGHRAAAGLTLEDAQVDDFRSDFCEAVAKQVAESDHVAEVKIDAEAGIGQLSYQSVRQIEQLAPFGQGNPRPVLYARGVQLAEPSRRMGGGDRHLTLRVTQDGVSIRGVAFGQGDWCEELNAHEGPFDIAYRPVINEFRGQRNVEIQLVDWRPTHAAVVGS
>NZ_CP036262.1|WP_145354932.1|1043820_1045293_+|RtcB-family-protein
MIPTGEATAILPAGNHHSPVKVFGNEKIRATFDDLCLQQAINSRCAPGVTEVVLNPDAHCGYGAPIGCVLASPTHIYPGPVGFDIKCSMSLLQTDVPADAMIDKTIRRELIHAVCRRIPTGMGKGARDVPKSRRVEEKTGVAAMTDGASSDVLAALGVPVAWADRCEDAFHRGHDGSADALRQRLYYLRQGKTFSRFRSTVQQLGSYGGGNHFGECEVVDVVDDNESRQIANVFGLRDQHVAFLSHCGSRGIGHRLASGQFKQLEHKFDQWKIPYPGNDKQLVYAPIGSSEANDYIDDMSLGANFATVNHLLINALVLEAFQEIIPGTTGNLVYFISHNIARQEIVDNRETWVHRKGATRAFPAGHHALKRTPFEHTGHPILLPGNPQAGSSVMVGLPGAKESCYSVNHGAGRALGRRRAIRELDQKQIDASFDSADILSNCRRYPRDEAPAAYKDFEEVLRSVKQAGLAKEVARLRARFVIKDSSDADD
>NZ_CP036262.1|WP_145350311.1|1045546_1046329_-|SprT-family-zinc-dependent-metalloprotease
MNEKERSKLGEMVLSLPAKNKDTVARQHQIYSDSLRISRAMDRPNFTRVANDDLRQMAKMYDELFFEGRLLKLAADEGLKFGWSSRMTKNAGKTVTLYPHNYKRGDRRKFEIILSSALLFQTFSDIDRPVEVTGIVCRDRLQAMQRVLEHELVHLVEMLVWDDSSCSKSLFQRIANRAFGHTQHQHDLITQRERAARKFKIGVGSKVNFQFEGQPLQGVVNRITRRATVLVPDQAGALFDDGKRYRKYYVPLEHLRKRSA
>NZ_CP036262.1|WP_145350313.1|1046525_1047872_+|twin-arginine-translocation-signal-domain-containing-protein
MAHTDEKSSHPSPQRSAAPRREFLKGAAALGGAAAALSVTAPKLHAAGSDVIRIALIGCGGRGRGAALNAMAADPKVRLVALADLFDQSITDCRKQLTKQKPDQVELSDETCFVGFDAYKKAIELADVVLLASPPHYRPDHLEAAVAADKHIFCEKPIATDATGVRRVLAICEEADKKNLNIVSGLCWRYDQGVRETMGQIFDGKIGRVIGSQANYLTGPVWIRPRKDGESEMAYQCRNWYYFNWLSGDHITEQFIHSLDKALWLRHDEPPVKAYGMGGRGLRSDLTQGDIFDHFAVVYEWADGSTTNAFTRQVRGAYNQVEDFVYGSDGKASVLANKIEGKNSWKFDGKDKVNMYQQEHNELFEAVQGKRPRINNGTYMCRSTLLAILGREVCYSGKEITWDEAINSPQDLRPQKYSFDAEAPAVKVPKPGVYKFPIAKPGDKSGSV

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Crispr_ID: NZ_CP036262_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_7

1380368-1380512

Orphan

Consensus_repeat	Method
GCCGGAGCGGCATCGCTGTCGCTCTTTGATCCGGCCTACTTTTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_7

>merge|NZ_CP036262|7|1380368-1380512|CRISPRCasFinder
GCCGGAGCGGCATCGCTGTCGCTCTTTGATCCGGCCTACTTTTACTCAAGCGACCATTAAACTGACACTTGCTGGCAATGAATGCCAAAGCGCGAGCGTCTGCCGGAGCGGCATCGCTATCGCTCTTTGATCCGGCCTACTTTTA

>NZ_CP036262|7|6|1380368-1380512|CRISPRCasFinder
GCCGGAGCGGCATCGCTGTCGCTCTTTGATCCGGCCTACTTTTA	CTCAAGCGACCATTAAACTGACACTTGCTGGCAATGAATGCCAAAGCGCGAGCGTCT
GCCGGAGCGGCATCGCTATCGCTCTTTGATCCGGCCTACTTTTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145350619.1\|1369178_1369652_-\|DUF1569-domain-containing-protein	unknown	unknown	gnl\|CDD\|369441
NZ_CP036262.1\|WP_145350634.1\|1399466_1399952_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350632.1\|1397219_1397669_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350633.1\|1399227_1399455_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350621.1\|1371805_1373059_-\|diaminopimelate-decarboxylase	unknown	unknown	gnl\|CDD\|143501
NZ_CP036262.1\|WP_145350624.1\|1376017_1376896_-\|UDP-N-acetylmuramate-dehydrogenase	unknown	unknown	gnl\|CDD\|237553
NZ_CP036262.1\|WP_145350618.1\|1367836_1368946_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525
NZ_CP036262.1\|WP_145350626.1\|1377799_1378852_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145355009.1\|1387375_1388506_+\|TIGR03009-domain-containing-protein	unknown	unknown	gnl\|CDD\|274387
NZ_CP036262.1\|WP_145355007.1\|1380570_1385706_-\|LEPR-XLL-domain-containing-protein	unknown	unknown	gnl\|CDD\|380149
NZ_CP036262.1\|WP_145350629.1\|1391774_1393193_+\|pyruvate-dehydrogenase	unknown	unknown	gnl\|CDD\|237000
NZ_CP036262.1\|WP_145350617.1\|1366800_1367679_-\|haloacid-dehalogenase-like-hydrolase	unknown	unknown	gnl\|CDD\|378932
NZ_CP036262.1\|WP_145350623.1\|1375054_1375966_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350630.1\|1394076_1395594_-\|DUF4038-domain-containing-protein	unknown	unknown	gnl\|CDD\|379072
NZ_CP036262.1\|WP_145350625.1\|1377026_1377434_-\|thioredoxin	unknown	unknown	gnl\|CDD\|379399
NZ_CP036262.1\|WP_145350628.1\|1389017_1391744_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	unknown	unknown	gnl\|CDD\|236500
NZ_CP036262.1\|WP_145350627.1\|1385964_1387074_-\|WD40-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP036262.1\|WP_145350622.1\|1373185_1374919_-\|S1-RNA-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|235851
NZ_CP036262.1\|WP_145350620.1\|1370384_1371479_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350631.1\|1396595_1396928_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145350619.1\|1369178_1369652_-\|DUF1569-domain-containing-protein	gnl\|CDD\|369441	pfam07606, DUF1569, Protein of unknown function (DUF1569). A family of hypothetical proteins identified in Rhodopirellula baltica.	1.25352e-46
NZ_CP036262.1\|WP_145350621.1\|1371805_1373059_-\|diaminopimelate-decarboxylase	gnl\|CDD\|143501	cd06828, PLPDE_III_DapDC, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Diaminopimelate Decarboxylase. Diaminopimelate decarboxylase (DapDC, EC 4.1.1.20) participates in the last step of lysine biosynthesis. It converts meso-2,6-diaminoheptanedioate to L-lysine. It is a fold type III PLP-dependent enzyme that contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. DapDC exists as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Homodimer formation and the presence of the PLP cofactor are required for catalytic activity.	6.38987e-153
NZ_CP036262.1\|WP_145350624.1\|1376017_1376896_-\|UDP-N-acetylmuramate-dehydrogenase	gnl\|CDD\|237553	PRK13905, murB, UDP-N-acetylmuramate dehydrogenase.	1.98549e-79
NZ_CP036262.1\|WP_145350618.1\|1367836_1368946_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	3.44808e-51
NZ_CP036262.1\|WP_145350626.1\|1377799_1378852_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	3.88924e-17
NZ_CP036262.1\|WP_145355009.1\|1387375_1388506_+\|TIGR03009-domain-containing-protein	gnl\|CDD\|274387	TIGR03009, plancto_dom_2, Planctomycetes uncharacterized domain TIGR03009. Domains described by this model are found, so far, only in the Planctomycetes (Pirellula sp. strain 1 and Gemmata obscuriglobus), in up to four proteins per genome. The function is unknown. [Hypothetical proteins, Conserved].	1.62561e-52
NZ_CP036262.1\|WP_145350627.1\|1385964_1387074_-\|WD40-repeat-domain-containing-protein	gnl\|CDD\|238121	cd00200, WD40, WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from its N-terminus and the WD dipeptide at its C-terminus and is 40 residues long, hence the name WD40; between GH and WD lies a conserved core; serves as a stable propeller-like platform to which proteins can bind either stably or reversibly; forms a propeller-like structure with several blades where each blade is composed of a four-stranded anti-parallel b-sheet; instances with few detectable copies are hypothesized to form larger structures by dimerization; each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade; the last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure; residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands; 7 copies of the repeat are present in this alignment.	8.29126e-44
NZ_CP036262.1\|WP_145350629.1\|1391774_1393193_+\|pyruvate-dehydrogenase	gnl\|CDD\|237000	PRK11855, PRK11855, dihydrolipoamide acetyltransferase; Reviewed.	9.34335e-151
NZ_CP036262.1\|WP_145350617.1\|1366800_1367679_-\|haloacid-dehalogenase-like-hydrolase	gnl\|CDD\|378932	pfam12710, HAD, haloacid dehalogenase-like hydrolase.	2.34099e-09
NZ_CP036262.1\|WP_145350628.1\|1389017_1391744_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	gnl\|CDD\|236500	PRK09405, aceE, pyruvate dehydrogenase subunit E1; Reviewed.	0
NZ_CP036262.1\|WP_145350630.1\|1394076_1395594_-\|DUF4038-domain-containing-protein	gnl\|CDD\|379072	pfam13204, DUF4038, Protein of unknown function (DUF4038). A family of putative cellulases.	5.44123e-81
NZ_CP036262.1\|WP_145350625.1\|1377026_1377434_-\|thioredoxin	gnl\|CDD\|379399	pfam13899, Thioredoxin_7, Thioredoxin-like. Thioredoxins are small enzymes that participate in redox reactions, via the reversible oxidation of an active centre disulfide bond.	7.62079e-10
NZ_CP036262.1\|WP_145355007.1\|1380570_1385706_-\|LEPR-XLL-domain-containing-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.	5.46475e-44
NZ_CP036262.1\|WP_145350622.1\|1373185_1374919_-\|S1-RNA-binding-domain-containing-protein	gnl\|CDD\|235851	PRK06676, rpsA, 30S ribosomal protein S1; Reviewed.	2.24259e-114

>NZ_CP036262.1|WP_145350626.1|1377799_1378852_+|Gfo/Idh/MocA-family-oxidoreductase
MRLRVGLIGLGDAWKTRYRPALKLLHDRFDVRAIYTNVPWLAAHAATDFQAQLADGYRSLIQRSDIDAVLILEPCWQGWLPMLAACDQGKAIYWAADLNFEAQQSREVKSKVDASGVAFMAEFPRRFAPATLRLKELIATRLGQPKLIFCHQRMPNAGDSKRTPAQRNGVPQAAANSDREILESIDWCRYVVGRDPVDVYAREHRSGERVDYRSLSMGFQATESAPAVTAQLSVGTYIPTQWHEAIHFRAPSAMQICCENGVAFIDLPSSLVWFDEAGRHLESLDSEMSVGEQLLTQFHRAVTSLVRKMGDLEDAWRASQVLHAGRLSLETQATIKLTLDGNECQLAPKL
>NZ_CP036262.1|WP_145350625.1|1377026_1377434_-|thioredoxin
MVSLFLAAVLATVVSDQPVTQQNYAQAYQSAHDEGKPLVVVVGAEWCPACVTLKEQTIAQMKAEGEFSEVSMAIVDQDAEPALAAQLKRGQSIPQIIVFSPQTSGGWKRTQMTGFQTRATIRTVLKRAKQRILGS
>NZ_CP036262.1|WP_145350624.1|1376017_1376896_-|UDP-N-acetylmuramate-dehydrogenase
MPFPEHLQHLIQNDQPLAQLTWLGIGGPARYFAEPHSREQLIELVQAASKAEIPVRLLGSGSNVLVRESGFDGLVLSLAASSLSTVSVAENQLTAAAGAKLSHAITHAVGEGLGGLEHLAGIPGTVGAAVSGNVSAAGGDIGSLVEQVEVMETDGTIRVIPKEDLQFSYRKSNLSGLLILSVTFALEKNDAIKLTKRLQKFWIVAQNQRPDGEPRLAQPFIDPDGFSADDLIQQSGMGGMRLGNASLTAGKPNYLLAHSGATSDDIVQLLARVREQVSSQSGIDLQLNLQIW
>NZ_CP036262.1|WP_145350623.1|1375054_1375966_-|hypothetical-protein
MAKAKAPDPSDKPHPIKHFLLGLVRKIAKAPLSVAFLWPVLLAIAAYVAWIQWGVDHVVPHFSRLESSHIQLTERPDYIPEHVDLTAEVLAGTGMGDLSLLDRQVSARIAEAYSTHAWIEQVKSVRVGVGGEIQVHVQYRQPVAMVRHLSRHPDVQGWAYYPVDRMGIVLPPDSFGGKEAEKYLVINIPEVDPRGTEGVSIGDSRVVLAASLAAILMPHREELGLAAIELHPTTGANRHRIEFDVVTQSGRRLVWGSPPGEELMNEPPADLKLKALFQSPPPGTDLRMAALAAHRKQIANDVQ
>NZ_CP036262.1|WP_145350622.1|1373185_1374919_-|S1-RNA-binding-domain-containing-protein
MTVGENPESQPAPETPDSQPAPAATDPPAPAAEKDSSAAGEATETTAAPPASEQPAAEKPAAELGPLSAAARRSGPLAARGAGAARPTSPASAPATSKASGGAQKPGNAPAVKPQFAKPPGSGSGRPTTGKPGSGPRPGSKRPGGNKKPDQPNPLQAPQPNRARITIPSKRSPLADDIQQELDAELAGADFDALMSGMPDRKGGLAEGQRVHAAVLKIHDDSVFVSLGGPDEGMIPFEQFEEEPTVGQSIEVIVRGFSSEDGLYLCVIPGQTISVSDISDLEEGATVEATVTATNTGGLELTVGGAPAFMPISQITEHRIEDTSDFVGQKLVCVITECNPGRNRLVLSRRAVLERERAERRKEQMEQLEVGQMHEGIVRSIKDFGAFVDLGGCDGLIHISKLSWDRVQHPSEVLEEGQKVKVRIDQFDKETGKIGLSYRDLITNPWDTVDTDYPIGQVVNGTVTRVANFGAFVKLGPGIEGLIHISELAHHRVSRVNNVVQEGENVEVKVMSIDTESQRVGLSLKAATAAPVETKSDSAPEEIDEPVREPIIKPQHTGPLKGGTGGDSGGDRFGLRW
>NZ_CP036262.1|WP_145350621.1|1371805_1373059_-|diaminopimelate-decarboxylase
MSSLPFSEEVIVDAAAEFPTPFYLYDETGIRENAQRLIKAFDWCDFKEFFAVKATPNPAILKALAEEGCGADCSSLAELVLCERIGIRGEEIIFTSNDTPAKDFEKAVELGAIINLDDISHIDYLDQICGLPELLCFRYNPGKPLGSDTAFIIGEPQEAKYGFTRDQLFAGFEDIRRRGVKRFGLHTMVLSNELNSSYFAETAKMIFEVAVDLKKELDLTLEFVNLGGGLGVPYRPEQEPIDLQTISDGIRQLQQQMLVPAGLGSMRICMENGRVMTGPYGVLVTRVLHQKQTYKHYVGVDACMANLMRPGMYGAYHHLSVMGKPTQPDDAPCDVVGSLCENNDKFAIDRPLPAVETGDIIAIHDAGAHGHSMGFQYNGKLRSAEYLRTTDGTIKQIRRAETLDDYFATLDLPTQGQ
>NZ_CP036262.1|WP_145350620.1|1370384_1371479_+|hypothetical-protein
MCRLGRYEVFAEKEVGVYHVYNRTVRGGFLHGVDPDSGVDHTPRRDRFRDRMKFLSKFLYVDVLSFAIMSNHWHCVFRNRPDLVEKLTDREVAVRWLSVLSRKRVPKKHRGKIQESEIAQIVNDPKRVAELRSRLSSISWFVRLMCQTIARECNIEDDCTGRFFEERFKLKRLLDEADVLACMSYVDLNPIRAGLTDSLEGYLEVSIGERLRTLDDGQIDSSSWLAPLELASEVDGEKVRVVGTKQAEPLSANKKQEARRGCLPMRLEAYTSLLWHLALEARPELQALESLTKQKLQTPICLRGEEISIAEFSERNLDLDRRCKTGLGKHTCRVIRERIAAQEAARQKSAGVGLSPRTIVSSQI
>NZ_CP036262.1|WP_145350619.1|1369178_1369652_-|DUF1569-domain-containing-protein
MDRRDLLFRNLDDAVADCKMLSESGYVRNGNWSLGQICLHMRLTIDANMDGYPLWMSVGLPLRPVLRKFLLPRLLRGDSPTGLKTAGIFVPPADANDLTEIEAFAKCVDRFHSHSGRLYPHPGFGRLPKDEFEQFHAAHTSHHLSFLAPRTEDDSSN
>NZ_CP036262.1|WP_145350618.1|1367836_1368946_+|GntR-family-transcriptional-regulator
MALESKHQLISRTLLKEIAAGEYQPSGRLPSETQLVKRFRVSRPTVARAMRDLQDQGLVERRAGSGTFLRRGNVATVGQRDLGLLVPELGTVDVLQAICGDLTRLARLHNFNLLSGEHDSIEAVDFGFQAAEALCADYIKKGVRGVFFAPFESSMHSSDWNRKLAAQLRDAGISVILLDRDLGKFPVRSEFDLVGIDNFAGGFVMTNHLLRLGCKQLVFLAPRTEVPTVRSRISGAYEAVRSGGISTSDELVQRVDPEDVGAVQQMVAETGCRGILCANDRLAVNLMQTLKSLGIRVPADIRIVGFDDVEFAASNTIPLTTIHQPCRDLAAVAFRAMVDSIEERDITPRSYVLPIKLIVRESCGVYREQ
>NZ_CP036262.1|WP_145350617.1|1366800_1367679_-|haloacid-dehalogenase-like-hydrolase
MVLHPPISPGPRSKPYLLASDFDHTLSFNDSGVALSEMLGQSSFAEKVNGLAASHLVQQGGELTYLLLHDPEYRCVRREHLVEVGKRIRLKKNLATLLEALESKIAGHQFLFYVISAAPEEVIQSALDGIVPPERIRGTRFNYNDATGEIESVSQLTAGYGKVAVLTELQQSIGLGPKRTVYVGDGSSDIHVMLHTNHCGGYTIAVSENPHIAPIAKRTVLSDNALSILIPLLEDVVGWTDPTAIRSLFSSCGLEVQGWDRTQMDRLTISETVPSGDTGPDQIYSGRASLAS
>NZ_CP036262.1|WP_145355007.1|1380570_1385706_-|LEPR-XLL-domain-containing-protein
MTAESLEPRILMAADPIHVGLVYIETDYLESDSDVGSDSHGDRFILSFTGGAADTELTEIRISTDKDGDGLSVGDPIFDTEVGNRGKKGAHGFKVHKITSDDAVQATATVEDGGQELIIRLEGFHAGDRLEFTIDVDEILRNVADIAIFNEKLDVITSGQEFEDSILEATFKAPHYESANADALFLNEFGDPGADFGLNLPPDEGSGVDSHADRSAAAVGSVTQTPKPISIAGTVWVDNDLDLLRETGEEGLPGVELTLLQRNESSGQFVDTGFRTTTDSAGNYQFGTSLGLMPGTYRVAESQPDGYFSVGAVPGNVDGSSVGTALQDDILTDIVIPKGDLHAVQYNFAEAQPSEVSGYVYRDDSDDGIRDPSEPGIANIRVRLIPESTLANQATLIATTDDNGFYQFEGLSPGQYRIEQIDQPVGLSDGLDTAGTVNGTTVGAATNPGDLISGLVLAGNQTGLEYNFGELPLGSISGMVYVLGPGEDCDGYDPGIDAPLPGVRVVLQDGSGNTIMETTTDNNGEYFFGQLPKGQYTILEFTPAGLIDGHSFAGRINNLKVGEAIDGGRIESIMLPAGGDGIRYDFCEASPAEVSGHVYHDRDQDGNRDSGEEGIADVLIELVDTQGTVIATTQTDGNGYYVFEDILPGTYAIRESQPAGYLDGLDQAGTIAGATVGTAANPGDLIRSIAIKQGQTGVNYDFGELLPASLSGHVHVDTDGDCIADPDEEMLEGVVIQLWNQAGEKIAETLTDSNGRYQFVDLVPGRYTVIELQPEGYFEGGQMAGSAGGDDSQINRIGDVDLGSGEIAVEYNFCELPPAEISGYVHADSNGDCILDPGEPMLENVRVDLLDANGNILATAYTDSNGYYRFTNLMAGQYTVRETQPIGYLQGHQTAGSAGGNDSSQDVISEIPIGYGDRLTDYNFCELEPSSLGGFVYVDSNENCVFESDEKPLGGVEVQLLNEAGEIIERTTTAADGSYRFENLRPGEYSVRELQPVGYFQGGQVVGDGGGIVLGQDHLGKISIGPGERLSQYNFCELEGGSISGMVWSETDLNRDFDSGDQPLADVVVELLNENGDVLRTTTTASDGSYTFDNLRPGNYQVREIQPGGYFHGGQNLGSLGGNVGADDLLVGIQVAGGKDGVDYDFPEVPPAIISGFVFQDGPAITLENPPTPEELRDYVDGIRGEDDTMLAGVWLELRTVQGQPYASSNALPGSYADGVIRVQTDINGFYEFTGLRPGAYSIYQIQPEDFIDGLDTPGTSGGLAVNPADIADDIDLQFIVQTLSASDETNPNDDAILNVDLVAGGRSQENNFSELIIKELPPSVPQPDPDPLPLVIPPYVPNTFPDSDRLAGFGVPEYVKPPAFYDLAYPVTWHLSIINAGSPRGEMQEDGAIIRQTSSQDDPTFATNQHRTGRWNLVTRTGERLSLSDAIILGDEGAIPLAGDFDGDGRDEVAIFVGGQWFVDLNGNGRWDPGDLWISLGTEADRPVVGDWDGDGKDDVGIFGREWLRDPQAIVNDPGLPDPGNRRSTRPKNLPPTAPEATDGMREMRRSTQPIRADLIDHVFRYGQHQDTPLAGDWNGDGIDAIAVFRAGVWQLDEDGDGRWTNADREFEFGPPNGVPVVGDWNGDGIDDFGVVLGDQWILDSDGDRKLTDKDERLQVPVAGIDALPIAGDWDGDGKDEPGSYSTQQEVPTDESTASDEGTRHEDDAA
>NZ_CP036262.1|WP_145350627.1|1385964_1387074_-|WD40-repeat-domain-containing-protein
MKIDWFRWGSVLLIAFASNLLVAQPHANGQSTSHRVAAVIPDLANVSEVLSLEPQDGSQASPVITALAVDPAGQVLIAAGDDHHLRVIDPHPFEEAQVLRKHTDWVRSLDFRNDGKLLVSAGNDGQIILWDREQDWKVLQTLEGAPAIASVCFAPQQGMLAAVGFDPQLFLLQQGGARRPVLRCGCNDLRVVRFSDDMRLVVAAGRSGNAHFFDPVSGQPAGEFELHSDRIRDLVFMPGSNVMVSVGEDRRIVVYDSLQGEILHTIPVLECKLFCVTPLDANHVAVGGADNKIRIVDIQRGQVKRSLSGHSGSIASVEASAEYLFSGSFDATVRRWPIAQILQAPLVAQRDDQSIQNEVSASKDPTPKR
>NZ_CP036262.1|WP_145355009.1|1387375_1388506_+|TIGR03009-domain-containing-protein
MRFLFVAVSCALAGSFAQGQAPANTAQRGYTAPQAGNGQAATSTAQNQNYQRQNQQLTPAQQHQLAQQRAASQQQAVRGTPTSASAGAAATAQMNTQQTEPKPPFAPLTAQQETELTQLLQAWEVQSNKVDRLECDFTRWHYDLVAAPAGVHATWAKGEIRYASPDKGMFKVNELKFFKGMQAGKPQYDVSEGQFGEYWVCNGQQLLDFDRGEKKCTIQDLPPEMQGTDIFESPLPFVFNLDANKIRERYWVRTVESPKKGMIVVEAWPKRQEDRAQYRLVQIVLDPQSFLPQALLMYAPNYNAQAAPAWDHYEFSNVKRNSIIGGLESFLNRFIEKPDKTWTIVRERYQPPAENNVPEGNRNIQAAQAPGGPQRQ
>NZ_CP036262.1|WP_145350628.1|1389017_1391744_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type
MADLDAKTIAQEELSNSMGERPHFDVDPAETAEWLSSLQYVLQSKGPERARFLLEQLRDSAALEGVQVPSETETPYVNTIPQKDQPPYPGNRDLERRIKSIIRWNAMAMVTRGNKKTDGIGGHISTFASSATLYEVAFNHFLQGRGEDGYSGDSIYFQGHASPGMYSRAFLEGRITEEKLENFRRELADGGGLSSYPHPWLMPSFWEYPTVSMGLGPIMAIYQARFNEYLRDRGIKDTSSQRVWAFLGDGEIDEPETLGAISLASREKLDNLIFVINCNLQRLDGPVRGNSKVIQELESIFRGAGWNVFKVVWGKDWDELLERDTSGLLVRRMNEVVDGQYQKYVVMPGSYIREHFFGKYPELLELVKNYSDERLERLGRGGHDPEKVFAAYHQAATLRNGRPTVVLAKTIKGYGLGEAGEGKNVAHNQKKLNEEELLEFRTRFGIPISDDEVGKAPFYKPPANSAEVKYLNERREALGGYVPSRPTEHPTMQVPTLEEYKKHTQDSKGKAASTTQMFVRLLTDLCRDKTIGKHIVPIVPDESRTFGMEGMFRQFGIYAHAGQLYEPVDSAQAMYYKEATDGQMLEEGITEAGSMSSFNAAGTAYSLHGVNMIPFFVYYSMFGFQRIGDLVWAAADMRAKGFMIGGTAGRTTLNGEGLQHQDGHSLLNAIAFPTVRAYDPAFGYEMTVIVLEGLKRLYQDGEDGIYYITAENDNYEHPAMPEGVEEGIIKGIYKFKSQEVDNAKARVQLFGSGAILNSALAAQKILAEKYNVASDVWSVTSYTQLRREAADCQRWNMLHPTETPKQSYLEKQLEGVEGPFISASDYVRALGEQLAPWVPGDYYVLGTDGMGRSETRENLRRHFEVDAESITIATLSRLSKVDVFSAQEVDQAITDLDFNRDKPNPYFT
>NZ_CP036262.1|WP_145350629.1|1391774_1393193_+|pyruvate-dehydrogenase
MATEEVKLPELSEGIDSGDVLEILVSEGDQITAGQDIVEMETDKATVPVSSSVGGKVVEVVVKIGDTVPIGGVLLKVDAAAAADAGSAAPEPAAPAATPEPPTPEPAAPEPAAQEPAAQEAPVAEAPAAPAPAAPVAPAPEPVAPTPPPAAPAAPVSDGAPIAAGPAIRRLAREVGVDLSTVQGSGAAGRITREDVLAVVRHASEAARSGVVVKAPSPAAPAVPGAEALPGDASSDAFGPVRVERMTKMRKTIAAQMHQSWSTVPRVTNFDDADITDLERLRGSSKEDYAAQGIKLTTMPFLIKAVATALRHHPAINAVIDEENGQVVYKDYVNIGIAVDTDRGLVVPVMPDVDRSGIPDVARGLAEMAAKVRNGQFGLNDLRGGTFTISNLGAIGGQYSTPIVNVPEVAILLVGRSRKLPVVMPDDTIQPRLMMPLSLSYDHRLVDGGTAARFLNDVIGYLEAPSRLLLAL
>NZ_CP036262.1|WP_145350630.1|1394076_1395594_-|DUF4038-domain-containing-protein
MMKSFLLCLVLLVMLGLPDSGKLGADDFASLRVSENGRFLVQEDGSGFFPVADTAWAIGWQLKRDQVERYLQRRKDQNFNTIALIAFPGVEGNVVIPNVYGDHAFKISGSGAWDPLQPITTPGKNPEDSAQYDYWDHLEYIIDTAESKGMAAILLPAWGVCVAGDWANGKATRDLIFDETSGYQYSHWIGERFKNKKNIIWMIGGDRSAVYGEKDYRKVFGAMAEGIADGVNGINQPNQEADYSTTLMSYHPRKWQPNSSEWFHNEPWLDFNSMQDQPSDQITATELDYKLLPAKPTWLFEGGYEFRRNIYKDWQIRFQSYQTVFAGGFGVTYGSMNIYHFNSAVAASDESITLDKSRKWEASLDEPGAMDMQHLFRLMTSMSNEQFLDRIPDQSLIEGSTGGMEGSEGIRSNRLQATRGSKGDYAMVYNANGRNFSVRMDRLSAPEMNAFWFNPRTGKWQVEDQDHTDRQPFKKSIPSGPAAPVQEFDPPGAEGDGNDWVLLLN
>NZ_CP036262.1|WP_145350631.1|1396595_1396928_-|hypothetical-protein
MTNTKMECSKCGSSILESTAGQNSGLCKTCVAGPKIETVAEGMELGMRLLLGLFFAALVGTIGYGIGSFLGTIGGIIVTIPFAFFGFVYGCFCVEINAIIRTLLPFISDP
>NZ_CP036262.1|WP_145350632.1|1397219_1397669_-|hypothetical-protein
MSRIKLLFVAVVTASLIAGTATSAFAIWIELQSASVPLSNDYPEYARQQIWKAFETENCDFIDGHSTLRVTTLNFSGDTTAVNKLLLELANCPAASVAVSFEKIKNKCDWRIVHSVTGNKFRVIINLESNQIELEQLTIPPANGPDLKR
>NZ_CP036262.1|WP_145350633.1|1399227_1399455_+|hypothetical-protein
MKTRSNRNRDHGPDPLLKVCTNELRHEERSPVKVASNESRVDDHLTVESRVFGNKVVVALVASDLIGTIEHMCRL
>NZ_CP036262.1|WP_145350634.1|1399466_1399952_-|hypothetical-protein
MTLNHLIRLVVTMVAGSGLCAAEAKQQMTVTLDVSKATILVDGELPLRYMTAAMDAVTDLGYDGATASQVTAAEQALSPTGVSFTVHIETDTVTFRSLRPVPTKVVICFLQRLDSASISNVRFATLDAEGANKCDTPSNASEPSNQVVSPVKDLSRRPGDQ

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Crispr_ID: NZ_CP036262_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_8

1513845-1513937

Orphan

Consensus_repeat	Method
CTCATGCCGTCGCGTTCGCGACT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_8

>merge|NZ_CP036262|8|1513845-1513937|CRISPRCasFinder
CTCATGCCGTCGCGTTCGCGACTTTTAAGGTGCTAGGGGGCATGTTCCTGGGACTTGCGTCCCAGGCTTTCGCATGCCGTCGCGTTCGCGACT

>NZ_CP036262|8|7|1513845-1513937|CRISPRCasFinder
CTCATGCCGTCGCGTTCGCGACT	TTTAAGGTGCTAGGGGGCATGTTCCTGGGACTTGCGTCCCAGGCTTT
CGCATGCCGTCGCGTTCGCGACT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145355027.1\|1509160_1510633_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293763
NZ_CP036262.1\|WP_145350710.1\|1511557_1513324_+\|serine-hydrolase	unknown	unknown	gnl\|CDD\|365903
NZ_CP036262.1\|WP_145355029.1\|1526586_1528620_-\|BREX-system-Lon-protease-like-protein-BrxL	unknown	unknown	gnl\|CDD\|379127
NZ_CP036262.1\|WP_145350718.1\|1525452_1526424_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350714.1\|1516854_1517946_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|197338
NZ_CP036262.1\|WP_145350707.1\|1505535_1507125_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293749
NZ_CP036262.1\|WP_145350705.1\|1501250_1503782_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350709.1\|1510734_1511436_+\|transposase	unknown	unknown	gnl\|CDD\|376616
NZ_CP036262.1\|WP_145350711.1\|1514332_1514959_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350704.1\|1500255_1501254_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP036262.1\|WP_145350717.1\|1523964_1525137_-\|SIR2-family-protein	unknown	unknown	gnl\|CDD\|379106
NZ_CP036262.1\|WP_145350708.1\|1507392_1508952_-\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP036262.1\|WP_145350702.1\|1496800_1498573_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|224331
NZ_CP036262.1\|WP_145350712.1\|1515843_1516464_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|222854
NZ_CP036262.1\|WP_145350719.1\|1528734_1531251_-\|BREX-1-system-phosphatase-PglZ-type-A	unknown	unknown	gnl\|CDD\|274259
NZ_CP036262.1\|WP_145350715.1\|1518386_1521572_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|379165
NZ_CP036262.1\|WP_145350716.1\|1522069_1523965_-\|DUF87-domain-containing-protein	unknown	unknown	gnl\|CDD\|223510
NZ_CP036262.1\|WP_145350706.1\|1504247_1504973_-\|GDSL-family-lipase	unknown	unknown	gnl\|CDD\|238858
NZ_CP036262.1\|WP_145350703.1\|1498569_1500225_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|132557
NZ_CP036262.1\|WP_145350713.1\|1516460_1516703_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145355027.1\|1509160_1510633_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293763	cd16144, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036262.1\|WP_145350710.1\|1511557_1513324_+\|serine-hydrolase	gnl\|CDD\|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	4.83705e-45
NZ_CP036262.1\|WP_145350714.1\|1516854_1517946_+\|hypothetical-protein	gnl\|CDD\|197338	cd10283, MnuA_DNase1-like, Mycoplasma pulmonis MnuA nuclease-like. This subfamily includes Mycoplasma pulmonis MnuA, a membrane-associated nuclease related to Deoxyribonuclease 1 (DNase1 or DNase I, EC 3.1.21.1). The in vivo role of MnuA is as yet undetermined. This subfamily belongs to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds.	3.35959e-34
NZ_CP036262.1\|WP_145350707.1\|1505535_1507125_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293749	cd16025, PAS_like, Bacterial Arylsulfatase of Pseudomonas aeruginosa and related proteins. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	1.35394e-174
NZ_CP036262.1\|WP_145350717.1\|1523964_1525137_-\|SIR2-family-protein	gnl\|CDD\|379106	pfam13289, SIR2_2, SIR2-like domain. This family of proteins are related to the sirtuins.	1.11594e-09
NZ_CP036262.1\|WP_145350709.1\|1510734_1511436_+\|transposase	gnl\|CDD\|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	2.33541e-16
NZ_CP036262.1\|WP_145350716.1\|1522069_1523965_-\|DUF87-domain-containing-protein	gnl\|CDD\|223510	COG0433, COG0433, HerA helicase [Replication, recombination, and repair].	3.0564e-25
NZ_CP036262.1\|WP_145350704.1\|1500255_1501254_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.07456e-95
NZ_CP036262.1\|WP_145350708.1\|1507392_1508952_-\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	2.95993e-38
NZ_CP036262.1\|WP_145350702.1\|1496800_1498573_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|224331	COG1413, COG1413, FOG: HEAT repeat [Energy production and conversion].	9.81282e-08
NZ_CP036262.1\|WP_145350712.1\|1515843_1516464_+\|AAA-family-ATPase	gnl\|CDD\|222854	PHA02518, PHA02518, ParA-like protein; Provisional.	1.98738e-55
NZ_CP036262.1\|WP_145350719.1\|1528734_1531251_-\|BREX-1-system-phosphatase-PglZ-type-A	gnl\|CDD\|274259	TIGR02687, conserved_hypothetical_protein, TIGR02687 family protein. Members of this family are uncharacterized proteins sporadically distributed in bacteria and archaea, about 880 amino acids in length. This protein is repeatedly found upstream of another uncharacterized protein of about 470 amino acids in length, modeled by TIGR02688.	0
NZ_CP036262.1\|WP_145350715.1\|1518386_1521572_+\|ATP-binding-protein	gnl\|CDD\|379165	pfam13401, AAA_22, AAA domain.	3.93011e-05
NZ_CP036262.1\|WP_145355029.1\|1526586_1528620_-\|BREX-system-Lon-protease-like-protein-BrxL	gnl\|CDD\|379127	pfam13337, Lon_2, Putative ATP-dependent Lon protease. This is a family of proteins that are annotated as ATP-dependent Lon proteases.	0
NZ_CP036262.1\|WP_145350706.1\|1504247_1504973_-\|GDSL-family-lipase	gnl\|CDD\|238858	cd01820, PAF_acetylesterase_like, PAF_acetylhydrolase (PAF-AH)_like subfamily of SGNH-hydrolases. Platelet-activating factor (PAF) and PAF-AH are key players in inflammation and in atherosclerosis. PAF-AH is a calcium independent phospholipase A2 which exhibits strong substrate specificity towards PAF, hydrolyzing an acetyl ester at the sn-2 position. PAF-AH also degrades a family of oxidized PAF-like phospholipids with short sn-2 residues. In addition, PAF and PAF-AH are associated with neural migration and mammalian reproduction.	4.88371e-86
NZ_CP036262.1\|WP_145350703.1\|1498569_1500225_-\|ABC-transporter-permease-subunit	gnl\|CDD\|132557	TIGR03518, ABC_transporter_permease_protein, gliding motility-associated ABC transporter permease protein GldF. Members of this protein family are exclusive to the Bacteroidetes phylum (previously Cytophaga-Flavobacteria-Bacteroides). GldF is believed to be a ABC transporter permease protein (along with ATP-binding subunit, GldA and a sunstrate-binding subunit, GldG) and is linked to a type of rapid surface gliding motility found in certain Bacteroidetes, such as Flavobacterium johnsoniae and Cytophaga hutchinsonii. Knockouts of GldF abolish the gliding phenotype. Gliding motility appears closely linked to chitin utilization in the model species Flavobacterium johnsoniae. Bacteroidetes with members of this protein family appear to have all of the genes associated with gliding motility.	4.07129e-07

>NZ_CP036262.1|WP_145350710.1|1511557_1513324_+|serine-hydrolase
MSPAKWIFERTLVAVRFEFRCGFPLLATVLSSPMTDFFCASPVLCERGLMSVVGIRRMARRLALYGVAFTLIVAASSGSSDAADRGSSTDQAATSPPGNPPQSVSRADVDAALRLIPERVEAMRQKSGVPGLAVAIVFDDEVVYSAGFGVRKLGSDDLVGPDTVFQIASLSKALSATVVAGVVGDGTIAWNDPIVENFPGFVLSDSYVTQRVTYADLFTHRSGLPAHAGDLLEDLGFDRQQVLTRLFRQPLSPFRGQHLYTNFGLTAAAEAAAVAAETRWDELMEDKLFAPAQMSNSSARFDDYLAADDRAVPHQRDIHGNWIVTTNQRDPDAQSPAGGVSSTANDLGQWLRLQLAGGELNGQRIIDPTALLTMQTPHSISGPPNNPSAHTNLYGLGMGISVRDDGYTTWSHSGAFLLGTGTNFSMIPGQRLGVVTLTNGQPVGLAEATSETILDLIVDGEVARDWLGGYMGRFAELYESDTPTDWTASVADPIPPSPLLTYAGTYDNDYYGPMTVDDSTGILVMTLGPKSMTFDLTPHDGDTFLFTPPGENSVGPTGITFDVKDGQSVSATAEFYDMTGLGTWTRQD
>NZ_CP036262.1|WP_145350709.1|1510734_1511436_+|transposase
MPRSPRADEAGGLYHVLNRANMRLPIFKKELDYVAFEKILHEALAIHQIELYCFQLMPNHYHLVLRPLVDGEMSRFMGWVGGTHTMRYHSHYHTSGQGHLYQQRYKSFPIQDDDHFFVVCRYVERNALRAEMVVRAEDWRWGSLWHWLQKPPVEPKLLSPWPISRLPNWVDRVNEPLTQSELDAVRLSAQRGRPLGDEGWVNTIARRLKLESTMRPRGRPRVRFPKQSQNKKA
>NZ_CP036262.1|WP_145355027.1|1509160_1510633_+|sulfatase-like-hydrolase/transferase
MRKRTTIITAFLLVGAAIPAVSADSQNKPARPNIVLVMADDLGGRDLPAYGNRFNETPNIDRLAVQGTVFHNAYAAPVCSATRASIQSGQYPARVGIFDFIPGHWRPFEKVIAPKHRTQHLPEDIVTLGDVMQSAGYKTGYFGKWHLNNGRENLPNTRGYEFAHMYAGGGFYAPKFVPPYDAGGDKRLSNQLTEMSIDFMKENKDQPFFLFLSHYDVHVQLDADKDLIDKYLDKKKTPDYPGNAVYAAMIEHVDNSVGDMMQATDELGLTDNTIFIFYSDNGGVDNRFDNVPLLTGKGKAAYPEGHPLTYIATSNTPLRAGKGTLYEGGIRVPLIVRWPGKVASGATSEAIVSSVDFYPTFLDLVQGKAPEKQVLDGFSMLPALTKNKFDTERELFTHYPVFHHEQPMSALRKGDWKIVQNLVSGEFELFNLKYDVNEMTDLKFSYAEKTAEMKKALAKWQSDTNAQNPVPNPDFDPSKRYEWGTHPDRK
>NZ_CP036262.1|WP_145350708.1|1507392_1508952_-|DUF1080-domain-containing-protein
MTRNFASLAMVIAVILSPLITCAAEPDLNPPEGFRAIFNAQDLSGWYGLNPHLVTKLSGEKKEASLKAQREEFSQHWRIENGELVNNGHGPYATSEEEFGDIEFLIEYKTIAKADSGIYLRGIPQVQIWDWHQTFDPKRPTRKPHLGSGALFNNTPGNSGRDPLVFADNPLGEWNQVRIRQVSDRTWVWLNDCLVVDGAVMENYWDRDQSLPATGPIMLQTHGGEIRWRNLFVRDIPADEADEILQASEEKKSDLSNSLTLHASFDQGLDADFSRGDRTCYVRAGKQLHRAKPTEEGKIESESGRYGGSLHFTKKGRFQPIFTNSGVLDYNGKEWNSTVSAWLRLDPDKDLEPGYCDPIQIVGDSGDKGFIFLEFSKDETPRYFRYAIRPLSSIWNPNNVSWADIPFDERPMVQVEKPSFSRESWTHVVFTLENINNRNAKPSGRLYLNGKLMGSIEDWDLTFDWDPASVLMVLGASYVGHMDDLAVFDRVLNGEEVEHLYGLEEGVKELYAPKTMQAK
>NZ_CP036262.1|WP_145350707.1|1505535_1507125_+|sulfatase-like-hydrolase/transferase
MKFRLLMAFALGLACLDVASSAEEASTRRPNIVLVMADDLGWSDVGCYGGEIRTPQIDSLARDGMRFTQFYNNAICGPTRASLLTGLYCQQVGHRGDRWNEPKNFDKCATIAELLQAGGYRTMMVGKWQGRDLAVDRGFDRFFGPMCQAKISYFHQVAKNPFRLDRDHWKLPSDFYLTDAINEFAVQFLDEAVGQSQPFFLYVSHIAPHWPLHARETDIAAYRQQYRESGWDQWRQRRLRKQRELGVIPANWEMSPRPANIHDWSADTNKDWQAERMAAYAAQVEAIDRGLGELLQIIQNSGQADNTLVMFLSDNGAAPDGGLNPTTGGFGFTPKTRNDRWRKDGEPIRPGSGPGNPPGPHDTFAAYGLAWANLSNTPLRGTKQTGYEGGICTPLVARWPGEIRSRGEVTNQVGHVIDIMATCLDVADVKYPTEFNDRRLLPMEGKSLLPILQGHDRDGHEVLCWSVPKHHVVRMGRWKAVQPRSGGAWQLFDLEADGTETVDLAEQQPERTRGLADRFHQWRQRVEAR
>NZ_CP036262.1|WP_145350706.1|1504247_1504973_-|GDSL-family-lipase
MPLRFRSVMNSFLLVALIAVSASAQDVATAPDTVKPVPRAGGWMNRHQSMNDRVKKGDVDLVFIGDSITQGWEGNGKNVWKTFYGDRNAVNLGIGGDRTQHVIWRLDNGNLEGISPKAAVIMIGTNNSGSNSPEEIAEGVEVIVKQLREKTPETKILVLATFPRGPNPADAKRQVNEKSNAIVEKLADGEHVFYLDIGDKFLDDDGNLSRDIMPDLLHLSEPGYTIWAESIEPSLTKLLGK
>NZ_CP036262.1|WP_145350705.1|1501250_1503782_-|hypothetical-protein
MFGPVVMKPPSLLFLLVGLAIWTGPAIGWAEDADGDAKNLPPIFVSSVGGPTGLKAYASGEWGEVSVVVGNRTQEPQVVQATVQIKGSEELRFSRDVLVPARSVRHSTIPIRLPEQLPPNAQLEILGHVAADARIPKAEFDGIVRLVSPSDTAYIQDHPISLEPSEPHLDFAYEAALALRAANGLDRRMMLCSERMLPSSYEGWDAVGSVILSGNRLAENPAARQALREWLSKGGCMWIQADKTSIDTIRLLLGSAVSIEQVDQVAIHDFAIQHASKDFQGDPTEVLLEQPVQFKRVIAEGVEVIYQIDGWPALMKAKVGLGEVYFSMLEGRGLIRPRRSEDPPAKNQQFHADYIGLEPLREVAIGMRPREIPEVVPVDVRAAYVTERIGYKIPSRGFVVGVLLGFCGLIGVAGVGLSYAGWREHLLWVTLATAGLATATVVAMGVASHHAVPATASSFQVVEVLPEMDEIATTGSIASYQPKLAAANMSSNGSTRLDPQSPRLAGKIRNIVWTDTNRWRWDKTIMPTGVQLFQFDRYQTLSQPVTATAAFGPQGLTGVVNADALRGTGRTEPVRLVDGVLVFPRSQPLAANLTPEGNFSAGIDDLLPPNEFFSSTFVDSTQRQRRAIYQAWYDSYQARLDSTSYLIGWTESLGSGLIWDEDVNVIGGALVAIPLTIQRTAPGTNISLPGSTLQVQSVVSKSGRSNTFENATSRWIFPYGRSARNRLRFQLPAEALPLRVDSASLFLDCSIPSRTLTIEVIEGEQRRTIVERANQSGKLTFDLAGPTPLKLDPEGGLTIEFTIGESPPTDDKAQQASNTWSIRTMRLDVSGTTMQSAEVEPQR
>NZ_CP036262.1|WP_145350704.1|1500255_1501254_-|ATP-binding-cassette-domain-containing-protein
MSELQPIVEIQNLTKRYGDFVAIDDLSLTVHRGQILGFIGPNGAGKTTTIKILVGLAKPTSGTARIAGVDCAKQSSTIKRLVGYMPDGFGAYDNMRVREYLDFFGAAFGIPRRQRQRRIAEVLEITSSTYMQDRFVESLSHGMQQRVGIARTLLHDPEVLIFDEPANGLDPQARIEMRELLLHLAACDKTLIVTSHILPELSRICDQVAILTHGRLRAAGSLEQIMHDLSQRRMIEIQLLAGEPPDQAKQVLQTILQADEPVTVSQAESMVRFETLRSDDALSEVLGKLIQAGVKIAQFRELQADLEDAFLSVIRQTEESQESPLPASTPSR
>NZ_CP036262.1|WP_145350703.1|1498569_1500225_-|ABC-transporter-permease-subunit
MLPIIRREFVAILRTRRAAIIQWLLAVCYTAIIVVRWPSDARADLSGANSQNVFGLFAYGLLAVVVLMTPIFPATSIVMERRTGTLALLLNSPLKTPAIYLGKLLGVLGFVVLMIAISLPSAAACYAMGGVDLQDQLVTLYGLLLVVAVQYVAVGLLVSSYAASADSAVRLTYGCVLGLSLITLGPYFLFQSDPGLVSSTVAWVRCLSPIPAVMQIAGQGDIGSLEKMQGWSALGRYVVLAMVSSLGMSMWTVYRLHFRCMDRSRSQGMVTDDKSLGIRAIRRVAFLVDPSRRSGSIGNWSNPVMIKEFRSRRFGRSHWMIRLVMVCAVLSLLIAFSVTAGTVRLELEAVGGPLVMLQVGLLVMFLPSLAAGLISSERESGAWPLLRSTPLSGGAIVRGKLLSVFWTMLLLIASTIPGYLVMLYIQPTVWVQVAQGFVCLILAGLLALMISATAGSIFRRTAAATTAAYICVLTLFGGSLLVWLARDAPFGFKTVENVLILNPMAAALSVFRIPGFAAYHLLPYSWYVSAALIVAMYFAMRLQVQRLTRPE
>NZ_CP036262.1|WP_145350702.1|1496800_1498573_-|HEAT-repeat-domain-containing-protein
MKVTVSRVMAWLTWATIWMCLALPCRAADDQSSNDPIVSPRYLEQPKIELKKPQIRWSPDLQNSWMQSLLLDEIDLKREASDALTLAQSLGMQALPEFRDVLWQIIDDDNTPVSCRVSAAQAYIAMGKPPANDELSAAVVRWPTALAIVLEPALAAWDSHLMRDIWLQRVQSDQADPALLRVAVEALGTVRDPASETALTALLQSSHQPFSLRMVAARSLSRLPGPHRVDLARAMLDAPLSAPMQWLLGVQLLGEEQSDEAIQLLERFADLDAPAVAGEALRQLLQVAPQKVIARAKQNIDDRDANIRAVTVDALITTGTLANIELLARALQDPVLTTRRTARDGLLQFASEEALTPEVVQKATTVLDSNDWRGIEQALILLTKLQQRDARQRLFQLLEHDRGEVMETAAWSIKELAQPDWSEQSLAALRKHLQNLTDAPTAAKLDALIHLVETMGVLRMPESLELLRTFVPKNSPFSPSVRGAAVWAIGEILQGQPNADVVSELQSRLNDNSPTLPESEIVRGMAAVSLGKMQSKASLQHLIRWRDSEQLNSFIGRRSAWAIFKITGDPIGKARTPTTNLRGWSVQPLK
>NZ_CP036262.1|WP_145350711.1|1514332_1514959_-|PEP-CTERM-sorting-domain-containing-protein
MFANHLSIVNFTLFTILTIGTSSFANAGLVLGFTGDYAPMNWTLDQNSGDGSVAISGAPASVSITSSNTGSGVFVNTDFSAIVTQSGTVSFAWEYLTTDSYASAEWDPFGYVLNGTFIQLTDDAGSISQSGNTAFLVSLGDVFGFRAQAIDDALGSATTTISTFSAPGTSNANVPEPFSIAIWGMIGLTGLAARKRHLHRTPSTEPMT
>NZ_CP036262.1|WP_145350712.1|1515843_1516464_+|AAA-family-ATPase
MIYSFLNQKGGVGKTTLSIHTASEFARRGQKVLLIDADPQGSALAWSNFRESPEFTVVGMPKATIHKEIEMLAEDYDHVVIDGPPRVTELARSIILASDIVIIPLQPSPMDVWASAETVDLVKEAQTFRPKIKVCMAVNRKIANTAIGRDVRKALKELKVPVLKSDIGQRVAYAESAAIGSTVLGKRMSKPAQEVKKFVNELRRIT
>NZ_CP036262.1|WP_145350713.1|1516460_1516703_+|hypothetical-protein
MSKQVNMSARPKVTPSPDTWVESRQVPEVKSTTKPKRLTIDLDPQLHKALKLSCVKREIQIADLLRGLIEEDVKQAKELP
>NZ_CP036262.1|WP_145350714.1|1516854_1517946_+|hypothetical-protein
MPHYYDLLPAQELEERGYPRFVSRMSVSEKKRAIKQVLAIKEHIVASGVPRKQDGNLVFATWNLKEFGQAKKHPEFYCYIAEIMFAFDLVVIQEVRRSIRELQILSNMLGDSWTYVINDVTEGNAGNGERSAILYDTKRVDFSGFSGELVVADGHQIKRTPHITGFITGWKHFSIINVHLDPGNSSTNAAERKGELKRIMNTLEPKVGIGGLGFENIILTGDFNFYPQVDDASVAMLKNDYGFEQVENLSDVDTTLAMNTHTYDRMFIRRDEFFEIAKDKDGNENGRVVEFRTLFESNLITYKAKAKADYESRNPTKTLDDNAYPNYFWVHWLSRQISDHYPIWLEINTDSAVRYLENKLDAL
>NZ_CP036262.1|WP_145350715.1|1518386_1521572_+|ATP-binding-protein
MADWIENHKIAWPAIVAVVSFFGGGFFRFLYERYFSERAVPTEKLLKRFAGNRLGSYGRRRLRNESLQALAGWHAELVPPAIGHKLRAWPETEFSVVEKDFSDGVTASRCPRLEDEEPSYRPLYISATSAAESLADSRSVVQSVIGQIKLVADNQEGSAALIKYRVADDRRPARLWVSAPQLQVTSTHQIYSLSQDLAKEVRRWIPSVSIVVEVYMSDDIQLDFEKAAESNSATIVKQLLGEDVFDDAFLRQASNSSEAYAIARTFAFYMLKQGAILDVAEPSMSYPVTDDILDERFKTHFANGVLTPGKWECVSIFGPPGSGKTDLARKCAAYLVSEHKSLIVALSTEGSLAALDFLTRGQNEEEARQALSSAVKRFVPTERSEDASWVKGCLDAFVRCSQVSPDRLVFLIDDLLPRPNLKEIITGITSNDSARKPKLILIGRPRLDFLPRPNSVYVECEHWGRGDATKMLRSWVEEGLKTHAAKALKAGWAAKRKAFSIYHLRVLVQYVDRPDLAPSTFMREELQRMTAPLTEHFVGLSRPPEQTLSDIRTMIESAIPSSEILEALDDHKPVDIVSLLGQLSWNSKYHEVAWSSGRTSGDLQALMNRDRVLSWSGKKIRDVEEADSFIRTCVEAGIFRQVRGEGGAHWIDNFIADGFAANYIGSDMLEGSYEIGDLTIADMVEKLHQRNSLDILPFALRSNQLMRVIRAVVLKKPHLADAVNSLLTDETVSAWLKEEPRLADDLTGALLAMASEIDLIQIGPLGVAFSEMTAISENAASLAKERLGKSDPGGMLALSGVAAESDSISGFFEQADSLGVDKTDSTEIAFWSAHKSRTPDFRKRIIQLIEGGTSMGEINRLWGRWCSSCEGPELANELYALLEGGVKDTSALSELVDQTCNAIADRSRGKRILDRAGFVAAIQHLHSQNEIDVAEVAVGWLGYFWNSGVCSRADRWSLDKVGSVAIQLDSQMPAKVSEVFSKLRAGEAVSLPSSSQLKQIGADTSTCPEIVSDRLPKRFSYTYELRPGWLMCVDKGETRYVDLTNELNKLKFQWRIEMIVQ
>NZ_CP036262.1|WP_145350716.1|1522069_1523965_-|DUF87-domain-containing-protein
MSSTFELVADLKVGDIVEVTGSSIKVELSGDVTELTRTHEGRVYPIGQIGSMVKIHFGRKLIFGFVTLLRMRSEEQTDLQSPIPPEADQRLMEVELFAEAVWNSTDAKLHLSRGVTTYPLPRQTVHLLTREETLSIYDTAEADRCDENYSPLVAFAHYSGADNAVCRANVDKMLGMHCAVLGSTGSGKSGAVAALLHSMVEHKQPNGSRSDPRIVILDPHGEYGRAFESCSVRYRAYDPLNNEAATGEPISLPYWLMSADEFRMLVIGKTEQEATSQNNIIYKALTHARMVAAGLVDKAPSSHGSPAPTDGLEFDSPRPKTASHSDRLLSFDRDKPRPFCLDELYRHILFMQAARDNKGTMRPITATEFSRSFKSIIDKLSVIRRDPRIDFLMSNWAKNSLRLEQIIGQLVGPSQAADGSEKPIRILDISGLPNEVAGPLASMLARLLFQYKLYQTDTERKRDPVLLVCEEAHRYVPDRGEAEYAAAQVAIRRIAREGRKYGIGLMLVSQRPSDIESTVIAQCGTWLVLRLTNAGDQQQVARFLPDGLSGMTKALPNLAQQEAIFVGEGAAMPAKVRVRDLRSDQLPKSNSAKFAQGWTLDRLIEREMKEVATRMVDGDQIEFAEDATKPF
>NZ_CP036262.1|WP_145350717.1|1523964_1525137_-|SIR2-family-protein
MELENGTSDVLQQLDNLLSSSNQSWLFGAGTSIDSGIPLMRALTDRVIARANEAPDGQALAGIQEELDPHCHIEHILSHIADRRAIAERCKNKQVQFGKAKFDLTTLEEFHRRLLCSIAETVRWGYIAYNGEDRPERVGTSHAPIVTIDNQTAFVRAVFNHRQTNVDKRRKPVRIFTTNYDTLIEDALAMECISYWDGFEGGAIGFRSLRFGDDEPVSGIRAQVIKLHGSIDWHLGSDGRVWRVRDSDVYPEKTSRVLIYPQSTKYVATQRDPFASQFDLLRRSLNSTKENVFAICGYSFGDEHINQEIQLAMERRENKTTILAFASKMSGVLNDWANSTWCKRLYVITEKGIFVGGNGPFAQPLKEQTLGWWKLDGVTRLLQSGPEACV
>NZ_CP036262.1|WP_145350718.1|1525452_1526424_-|hypothetical-protein
MCKTAFSELIRLYDDFDDQLRFYYEQHFSVESHYECALRDCQWPDCELEAADGICPKDIPIPQSHQKITRDHALNVAATSLCRELGIARLPADKKAQPGRNFRKLLVASGQLPLGSARREGFEQELKDDISLAVRNAIYELRDWIDQQKNELQHDLTRPHRLHVDDLDSFSLVKDVSSRAANGMLRNGVLDWPEDRIRTAFEEILDIPFTSRHSPAELNDLITANVILDGLRVPTAFMLKGPGVKVSTLEIKHCGSQGNQLLKLFDSPAEIFSIQFVGKISESVVRDAEQKAQNLRRLGKQASLLVIDGQDTARILIAYGKTG
>NZ_CP036262.1|WP_145355029.1|1526586_1528620_-|BREX-system-Lon-protease-like-protein-BrxL
MSPLDRKINEHFGGLVVRKDLVKAVKGNAVLPSYVLEYLLGQYCATADENSIETGIETVKDIVAKHYVTRSEAGLVRSQIREKKLRKVIDRISVNLNDKHDIYEATFANLGINKVAVPASTVKKHQKLLVGGVWCIADIEYQHDDDDKSIPWVLESLKPIQLSSFDFDGYLAARKQFTTDEWIDTLIQSIGFTPDAFGRRSKFLQLVRLIPFCERNYNLIELGPKGTGKSHIYGEFSPHGMLISGGEVSVPKLFVENRAPYKIGLVGYWDCVAFDEFAGKAKRVDKSLVDIMKNYMANKTFSRGIETLGAEASMAFVGNTQHTVAHMLRHSDLFDELPTKFHDSAFLDRMHFFVPGWEVDILRGDMYTSDFGFVVDYLAEILKQQRNFDYSHLYANDFQLSEQISTRDRDAINKTFSGLVKIIFPNQDATTKELEELLVFAIEGRKRVKDQLMRIDQTYADVRFAYTNAEGQEEVVKTLEEELYPAIYYKSGEPESDTEEVAHKIEPTKQSPTAAKSGAEEGHVTVKENQRGIDFDTLFGPYVVGAKKIVLTDPYVRIFHQARNLMEFIETIARVKPDDERVEIELLTSEEEFSPEKQLEFFEKIQKNCLPIGILFSWTFDTTIHARHIVTDTGWKILLDRGLDVFQRYDTNDSFAISNRLQKHRSCKAFEVTYLRQ
>NZ_CP036262.1|WP_145350719.1|1528734_1531251_-|BREX-1-system-phosphatase-PglZ-type-A
MSERIIQALEKLFTKHRIVFWYDEEDSLRKDFDAVEVAGVEKVEIVNNEFGLKYRMLRQQSKQKFLVFKTGGPPEDKENWLLDVQLAHTDFRTDKASLWLTELELPYEFRPLVSRHEFFFNSAKRRDSLKKKVTKNDTLTQVAMKMLGVCADCADSEPRLDSVIENLLAELAKGDGAKRYDLIGKCGLDGFLWEQTKNVYQYAADSPTVKDFAIELFKSCYRMDVGGEVRFGSEALVFLKRWKDSRNHEAAFKTLSHQAAEMLSISSDLENRDLKALAEVDYFEFVDQRILSELASAVGKKTISSGECTQLIRGRRRGHWYAQYEHYYEAVDHAAQLLHLLDTLSIQLDSLQQGVSAYIQSFYRLDQVYRKFIFHNVKSGGATLLGPLTNEICKRYTNTFLMPLGDRWQELVDGLEKWGIPGNRSQTGFFDKYVRRVLEKNKKVYVIISDAMRFEVGEELCRRVRQEDRFEAELDHMITTLPSYTQLGMGALLPHKQLRIQEDKSTTVIADDVSTAGTVNRDKILKAAAKSIASDASALAVQAVDILDKNKEEVRALVRDHDVIYIYHNSIDQIGHTQKTERKAFEAAETAMEDVVRVVRKLTSANATNVVVTADHGFLYQDEVDESDFSAAQVEGEILASDRRFIVGRDLKVSGGANLYSSEALGLDGDLQIAVPKSINRFRKSGSSTRFMHGGSTLQEIVIPVIEIKKSRGSDVSAVNVDMIPTPSSVISTGQLALVFYQSEPVTEKVQARHLRVGLYATDGELISDSHELAFDLTSENARERELKVRLLLSKQADNYNQQQIMLKMEEPISDTSQFKDYKSVPFTLRRSFTSDFD

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_CP036262_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_9

1567995-1568097

Orphan

Consensus_repeat	Method
GGGTGTGCAAAAGCACGAAC	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP036262_9

>merge|NZ_CP036262|9|1567995-1568097|PILER-CR
GGTGTGCGAAAGCACGAAGAGAAGTGGGCAGCTACACAGTTCGGGGTGTGCAAAAGCACGAACAGCCTTCTGCAGCCAGTGCCGAGTGTGCAAAAGCACGAAC

>NZ_CP036262|9|2|1567995-1568097|PILER-CR
GGTGTGCGAAAGCACGAAGA	GAAGTGGGCAGCTACACAGTTCGG
GGTGTGCAAAAGCACGAACA	GCCTTCTGCAGCCAGTGCCG
AGTGTGCAAAAGCACGAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145350745.1\|1574351_1575065_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350747.1\|1575764_1576481_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350743.1\|1570043_1571078_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350739.1\|1565358_1565904_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350734.1\|1555945_1556269_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145355037.1\|1564018_1565281_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP036262.1\|WP_145350749.1\|1578046_1578787_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350735.1\|1556271_1556931_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145355033.1\|1559426_1560689_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP036262.1\|WP_145350748.1\|1576493_1578050_+\|TraM-recognition-domain-containing-protein	unknown	unknown	gnl\|CDD\|226036
NZ_CP036262.1\|WP_145350738.1\|1562870_1563209_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350742.1\|1569567_1570047_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350741.1\|1568194_1569262_+\|RepB-family-plasmid-replication-initiator-protein	unknown	unknown	gnl\|CDD\|370826
NZ_CP036262.1\|WP_145355035.1\|1561442_1562705_+\|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl\|CDD\|275209
NZ_CP036262.1\|WP_145350737.1\|1557821_1558748_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275381
NZ_CP036262.1\|WP_145350740.1\|1566633_1567605_-\|DUF3991-domain-containing-protein	unknown	unknown	gnl\|CDD\|379044
NZ_CP036262.1\|WP_145350750.1\|1578811_1579054_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP036262.1\|WP_145350736.1\|1557242_1557677_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145350744.1\|1571479_1574296_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214621
NZ_CP036262.1\|WP_145350746.1\|1575102_1575732_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145350741.1\|1568194_1569262_+\|RepB-family-plasmid-replication-initiator-protein	gnl\|CDD\|370826	pfam10134, RPA, Replication initiator protein A. Members of this family of bacterial proteins are single-stranded DNA binding proteins that are involved in DNA replication, repair and recombination.	1.1755e-102
NZ_CP036262.1\|WP_145355037.1\|1564018_1565281_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	2.25358e-165
NZ_CP036262.1\|WP_145350737.1\|1557821_1558748_-\|hypothetical-protein	gnl\|CDD\|275381	sd00034, LRR_AMN1, leucine-rich repeats, antagonist of mitotic exit network protein 1-like subfamily. A leucine-rich repeat (LRR) is a structural protein motif of 20-30 amino acids that is unusually rich in the hydrophobic amino acid leucine. The conserved eleven-residue sequence motif (LxxLxLxxN/CxL) within the LRRs corresponds to the beta-strand and adjacent loop regions, whereas the remaining parts of the repeats are variable. LRRs fold together to form a solenoid protein domain, termed leucine-rich repeat domain. Leucine-rich repeats are usually involved in protein-protein interactions.	2.6111e-16
NZ_CP036262.1\|WP_145350740.1\|1566633_1567605_-\|DUF3991-domain-containing-protein	gnl\|CDD\|379044	pfam13155, Toprim_2, Toprim-like. This is a family or Toprim-like proteins.	5.10058e-15
NZ_CP036262.1\|WP_145350750.1\|1578811_1579054_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	2.43126e-14
NZ_CP036262.1\|WP_145355033.1\|1559426_1560689_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	1.29482e-162
NZ_CP036262.1\|WP_145350748.1\|1576493_1578050_+\|TraM-recognition-domain-containing-protein	gnl\|CDD\|226036	COG3505, VirD4, Type IV secretory pathway, VirD4 components [Intracellular trafficking and secretion].	3.4381e-31
NZ_CP036262.1\|WP_145350744.1\|1571479_1574296_+\|hypothetical-protein	gnl\|CDD\|214621	smart00327, VWA, von Willebrand factor (vWF) type A domain. VWA domains in extracellular eukaryotic proteins mediate adhesion via metal ion-dependent adhesion sites (MIDAS). Intracellular VWA domains and homologues in prokaryotes have recently been identified. The proposed VWA domains in integrin beta subunits have recently been substantiated using sequence-based methods.	2.6032e-05
NZ_CP036262.1\|WP_145355035.1\|1561442_1562705_+\|group-II-intron-reverse-transcriptase/maturase	gnl\|CDD\|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	9.94173e-162

>NZ_CP036262.1|WP_145350740.1|1566633_1567605_-|DUF3991-domain-containing-protein
MDRHSELAAFKRLDLVQYCQSRSFVIDQRASSRSAIVLRSPSDEKIGVSKSTEGTFIFYDYKGGRGGSIIDFCQWLDGGTLGEVRKTLRAYDPTSFSVPSALPFKLVSSTHDETKVLAAWMQARSIGASGHPYLTQYRRIALEVQTAPLFRDRIRIDSRSNALFPHFSTKGTLCGFEIKNGGASKKSFTGFSPNGLKGLACSRPRETDCEMVVCETAIDMLSLASIEGIEKRRFFSTGGQVSEMQLEALQSAASRMPTNSTRILLALDNDKAGHELARRIADALSNSKLKVVPYFPPDPGADWNDMLQRTIRESNRTPEPIKS
>NZ_CP036262.1|WP_145350739.1|1565358_1565904_-|hypothetical-protein
MRISLFCAASLAACLFAGTVAQALTMSYGRRDIAEAGAGCIGGWISGHGNTAYFQGDTAQLNQHLASLAADTEGRSAAKVVLHAGTKTVDNPEEEAQTVFRARTRADKQIPAQLSIDWSVRKYCPSDDLLTGRCKCDRRIVTVDIWVANDIRLDALSIPAGLKVESGRELERFVDRHSGSE
>NZ_CP036262.1|WP_145355037.1|1564018_1565281_+|group-II-intron-reverse-transcriptase/maturase
MQHVVADANFEAAWKSVKRNRGAPGPDGITIAEFPDWFRPRWLSIRQQLLDGTYRPDPVRRKTIDKPDGGKRLLGIPNIVDRLIQQAIVQILTPVFDPHFSDSSHGFRPKRSAHGAAKQVRRTVRRGYRFVADFDLSKFFDRVQHDVLMSRVARRVRDKRLLQLIGRYLRAGVMVEGVLQPTDLGTPQGGPLSPILSNILLDDLDKELERRGLPFVRYADDFAVFAKSPRAAERIMNSVGRYVAKKLRLVVNEEKSRVLACTEFEFLGFSFPKSRANINVSVKSILRFKQRVREITGRSRGISMDRRLGELRRYVRGWMGYFGIASQLKLFDKLDQWIRRRIRMCYWKQWKRPKRRRAMLIRLGVPRRQAIRHARSRKGHWRMAKTIASNVGLTNKWLQEEGLLSLKTLWAQLAPLRRTA
>NZ_CP036262.1|WP_145350738.1|1562870_1563209_-|hypothetical-protein
MATVQHQLEQLHGRLNRAGVPPDGCYKRNTVWYPLVSYINTIIALYLSDNYDVIPVFVMRATNTHADIAKEHKHVYLDLVAEYLHLIVTHLRETGFTEEQLAPYVSGVHGDN
>NZ_CP036262.1|WP_145355035.1|1561442_1562705_+|group-II-intron-reverse-transcriptase/maturase
MEQIVAPENFETAWARVRANRGAPGPDGITLDEFPELFRSQWAEIRQQLLEGTYQPGPTRRKSISKDDGGQRDLGIPNVIDRLIQQAVLIVLTPIFDPTFSDSSFGFRPNRSAHGAAKQIQSHIQAGYRHCVDMDLSKFFDRVQHDVLLSRVARKIRDKRLLGLIGRYLRAGVMVDAQLQPSIEGTMQGGPLSPLLANILLDDFDKELESRGLCFVRYADDFLVFTKTRKAAERVFDSVGRYLTRKLKLVVNQQKSRICGTHGVEFLGFEFRGLGGSIRVSPKNIAKFKERVKEITRRNRGVSMTSRLRELRPYFNGWVGYFRWVPIKSTFGDLDKWVRRRIRACYWKQWRKPKARVRKLLSLGIHRRVACSHGNSSKGPWLMSKTWAVHQALSMEYLTQSGLPSLLEIWSKFAAKKRNA
>NZ_CP036262.1|WP_145355033.1|1559426_1560689_+|group-II-intron-reverse-transcriptase/maturase
MEQIVDPENFETAWARVRANRGAPGPDGITLDEFPELFRSQWAEIRQQLLEGTYQPGPARRKSISKDDGGQRDLGIPNVIDRLIQQAVLIVLTPIFDPTFSDSSFGFRPNRSAHGAAKQIQSHIQAGYRHCVDMDLSKFFDRVQHDVLLSRVARKIRDKRLLGLIGRYLRAGVMVDAQLQPSIEGTMQGGPLSPLLANILLDDFDKELESRGLRFVRYADDFLVFTKTRKAAERVFDSVGRYLTRKLKLVVNQQKSRICGTHGVEFLGFEFRGLGGSIRVSPKNIAKFKERVKEITRRNRGVSMTSRLRELRPYFNGWVGYFRWVPIKSTFGDLDKWVRRRIRACYWKQWRKPKARVRKLLSLGIHRRVACSHGNSSKGPWLMSKTWAVHQALSMDYLTQSGLPSLLEIWSKFAAKKRNA
>NZ_CP036262.1|WP_145350737.1|1557821_1558748_-|hypothetical-protein
MLGVHAWEHGLRHFSQWIVNLPCPVMSTVLSLNLHMNLAESSLESSTKVSHRRWLRFSMRSLLFVVTVVSVWLAVVSSRARSQKQAIDRVKQLGGFVSYDYTLDTNMNWRKGPNLPAPVWLIDLTGEDYVRTVWIVNFDDKSDPSDDDLEVVERFDALKQLTLMNRKKITDEGLRHVSGLTELEVLALNGTNVSGEGLSHLRNCQGLKGLPMNNTPLMDVGLSHISHLGSLEWVQLSGTQVTDQGLSHLSGLTKLESLELRDTAITDDGLKHLSNLKSLKKLSLRGTETTDAGRNWLQAELPNCKVSN
>NZ_CP036262.1|WP_145350736.1|1557242_1557677_-|hypothetical-protein
MYRTAVFTLLTMLVGIPSILVADEPEQGQVATPAFDVTSLHRNIPSIAASRVSVAVSDVSLPTFVAGIELLLERDKELARELVAAVDRDNRPHQSTGIPTAEHRVLVTLESSISNTEFEQIVRFALADDARLARALIGVKTGNR
>NZ_CP036262.1|WP_145350735.1|1556271_1556931_+|hypothetical-protein
MQSNDSLKEQVSQLTGEVKVLRESVDELKTALEWAIRNARITVHFDETANSQPSQVAEPPPTPATHQKQLTLNFETQATFKVAEQLTASEQPGKNVLSIEDYKARTRAIWDAVNAWIIEFTPSIEFDAHELGVYEKIKPESQGSFSDEDQERLLKDDYALACGVAIAVEDASILMEDHGHADDAESLTRAYYLAIALKSADFDLEHYLPGFPVHCMERP
>NZ_CP036262.1|WP_145350734.1|1555945_1556269_+|hypothetical-protein
MDPTSTFNAMLEAYANSDHEEAREHATNLMDWLLKGGFPPRFFLAAKSQSVFELSTNFAEQASAEVCRRILRDDNFGPDETGGEYCDPEPSGPCHPSELIRNQCDLP
>NZ_CP036262.1|WP_145350741.1|1568194_1569262_+|RepB-family-plasmid-replication-initiator-protein
MTPQASASRQVLLPERYPEGDLFICDVSDAIPKSDLGSMEHPIFSLSTKPDTQQRVYDHAGVKITITPSSVGLASVHDKDILIYCISQLVAKMNAGEPLGRTLHIRAHDLLVTTNRSTDGRGYEQLIAAMDRLSGTRIKTNLRSGGEEITEGFGLIDSWRILRQTQSGRMSEMRINLSDWMFNAVQAREVLTIHRSYFRLRKSLERRLYELARKHVGRQHEWRISLELLRKKCGSNSTLKEFRRMIRAIAKDDEANDHIPDYSVRMELGADGKREMVRFQNRGTLPAMKTGPDIVVPPLDPDTYHEARLEAPGWDVYELEKQWRSWITMSGAEAPRNPDAAFLGFCRRWRQTKQL
>NZ_CP036262.1|WP_145350742.1|1569567_1570047_+|hypothetical-protein
MTKSSFYAGSMELPKGIESRLKKYQADPSLDCERAADYRFACEYLLQTAQIAWYGECNFSDLEDAIYWVDRLTNYPIDGFPDSSESGLSPEDLDEIHWRAQSWYEVFKATVASNPNDYKDDPSTLKEVIRRETDFFNFSESESDENEKTFADIGTLDYL
>NZ_CP036262.1|WP_145350743.1|1570043_1571078_-|hypothetical-protein
MPAIDLGTFNSLFDLKEMTIAKLARLSKVSRATIRNILKTGRCTEKTLHKISGPLGTTADCLIAHDRANTIICDVLKEEYKDLLRDVLHSDAFVVHAEETVGLFDADVLAFAHQVKKSDLDSCNLSPNGRNQVHTELCRDGLFYKKPNPHHPTIFKYCCRIWSLDQLTDNLELRIGIEILCAKRALKLIARDPAKSLAIQREMKRLLDGMEELKPSLESNPDDKIADLALRYDSRFHRAWAGDAPDHRASMGRAIFGHGQLTHHYKYEMAKARRKSNFPAKQTTLSDLALYSLNDLRGIYDAFVAIDDPTDSKQVDPLLDLIEQHPRNNWDRIAAIHQFNCENA
>NZ_CP036262.1|WP_145350744.1|1571479_1574296_+|hypothetical-protein
MLNGIPQGGNSNNHSSRNADRNAGHRRQSGRNGADAKPERSPPDHGQTELPKIGFKPVAGDSQYSPCELTDATEKMHRNCLPIEKISHSERNLKNLAENPGHYASVISQHQQIIASHLVMLEEVEACHKGLQEAKKKAKRRRDSAPPHKTHYSWNPRYRKQPGATSRRKRKSWSRLGILTFPSFRKWLGGFTDAGWFVVAIACMFAVIPLISVPLEFQLFATQITAGPLFDLPGATKTAPTIQPGFWVCASACFAPLICMLIGLKVIKQPGFFWSDQVTKWMGISLFLGALLALWFFAFVTCSTPGSSSITNRLPPSSSGLHWSLVALLSSVMALTNTFAISWAWDWFSKLLEAKVTKSVLLDQANQDLRKIGAAFVANQATKRQITGFLERCKSADPILQGALDKARQRLSSEQELAETLRSANTMLDHVNELLAKLKGGQTLAWMGFVLALTLGCHNAPPLQDGNQQAGAAAELPEIEYFVFDNGDFAPSTVRELLKDMVLSRLPGGARLYVVHGSDRNLAAAIDVPYGDQIQREANPYFAAEWQGIESFYSNPPVPTETTPSVIGIARSVQDLRRNKQAPCKIVCLGSIVYHDPEYAGFSMRNHQVPSTGWIGDKSGPFTDNPSLPRSTQVECFVPSGKVGDNLRHGQLIRDFSATYIASLNGAHLTRISPDLSLAGMFSESFMPVHSGQPAGEQVIIDTRVEDDVLPVETPRSREIITVPFDASALMPRLRWEEGSLQQVIQDGGGDPTKLSAMSCDVFVCVDGSGSMVRVLRDFGSTLDRICDDLGPVLGRLRIGVLVISDKASRQFPLQIVTGGSPSRAKLKEFTTDIGPLGGDPEMGQLIHAGSEAIKTGSTLDPNRRILIVASDYINGDITDLSSKVERWLALAPACNRVLAVCTSAEKSAQFQQLCNSENARAASGTDALIEELTNMTK
>NZ_CP036262.1|WP_145350745.1|1574351_1575065_+|hypothetical-protein
MSILDLLLKQSSGVGLGAKIVDQLSQEEHFTLVKQLEALTDREVSHVAGNLCDALTGARSLGYLRACGIVFVAMTLLSGPRQELIQEFEKEVGITRSKLYRMRLVWEVFGRRLKDQPAVLERFIPQALNKLAETWVSDDARDNAIAAAERGETINIKAAEKFTGRRPKPESSSTGKRSKASGPLFQHSSESVNVVIKRRSKGSAVDFQAIVLALEEALAKARQEMIDVNAGPLRISG
>NZ_CP036262.1|WP_145350746.1|1575102_1575732_+|hypothetical-protein
MPFEKLDSFTNPFGDSSEPEEVQESNDDLRLPASDVVVRKPLGKRLKYYAVNAIALPTGLIVSAEVSAAGLRSLLAVTQMPLSRLPISGAAQISQYQGIERLDLAILMAALLFAATAVLWANVFKCLAKPGQITADWKNRKAWLILRSVIAVTVLSSEAVLFYHGVAAEGGGGWTETPVYVPLVTSVLWIAAVAMLGAYHSDYVTEHKE
>NZ_CP036262.1|WP_145350747.1|1575764_1576481_+|hypothetical-protein
MSYFHDALKLLFTVLLICCSEGCVPVETDQSPAMFDSDLDDATLNIIVDTSSSFRRTFEMQGGPLMSKVIVDFMQQNAGKDIRITISQMQARDNVVLFEGGANEFRKQFKAPESLLELVESAAEPNTFSPVFVATGKSIRYANEYLAPSLKPGGRLLTVIYSDMVDTEPNRATRSQEGHQMLAELERYRGAGGRLALYCVTEEERTRWFKIVDLAGFERSDVAIFSDRVADPDLPQWY
>NZ_CP036262.1|WP_145350748.1|1576493_1578050_+|TraM-recognition-domain-containing-protein
MPKLHSLLADLPRGRRPGDIGARPDAHFEAPENLVATRSLRFDPAVNDCNKWFIGVVGGKAQQDGFTREGRPSRYVTGGVPLACAIDNHIFLLASSRSGKGRGVLGTNLALSPPGASSFVIDPKGDLASQFIRYHALAQEKVCGLIDPMLCADSRTREYRVGICPIRFVMGSGIEGLVERATIIADSFVPEDVNARERHWDEKAKMALGPIAAHLATHPLYEGIRNGVELWRAITQIAKPSLVDESRFSLDVEMMSSELEYVRDGARMLFDCSETEFSGIVSTLRRHLGFLSIQAIQNCMLLPVQHDPSVLASGGVSLFSSLPAKYQSTCAGWQRFIIQAHLAQFEEHRIRSRYQCTFYLDEFHTLGRMKVVEQGAALLAGLGVRLAVCAHSLGQIRNLYSENFEIFLSNAGVIQAFAVADQMSLEYLSKRLGNTSTLSHASSAATYGQQTGDGMGGDSYQVGSDPLMAPHEIEQYFGRDDSQLRQLILRPSHKPAITQRAYLDKHSIFANRFDEVHT
>NZ_CP036262.1|WP_145350749.1|1578046_1578787_+|hypothetical-protein
MIRIYRTAALPPYPPLYFDDSNGEIMIVGRHAAGWGLAMGGLIAQSLLYASSFWVAFKAWEWIGEYPFEAELVRQFVLLVQIFGAGIVMQVWFKVVKHCCVKTLKTWLAERVFYSTVRIYINRRQVGFKCRRYRNGVVLPRRLKARRIRLEFISTDDRIDPYGSTESQEQQMARRSKRCLLLVVSTWPQIASGKMPGPPDRRAFPIAEMPTSICRKFNTVCNAALRLSDPTFQPKPQSTVGQDIDA
>NZ_CP036262.1|WP_145350750.1|1578811_1579054_+|helix-turn-helix-domain-containing-protein
MPTMIRPVPHSEPLLLNVREVAAILAVSESTVYALIRQRKLSCYRFGRCIRIHRDAITEYLDSQRVECTPAEFLNAKRHF

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_CP036262_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_10

2304044-2304137

Orphan

Consensus_repeat	Method
GGCCGGACGGCTCGCGCCGTTCCGCTAAGAAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_10

>merge|NZ_CP036262|10|2304044-2304137|CRISPRCasFinder
GGCCGGACGGCTCGCGCCGTTCCGCTAAGAATGCGTACCGCCAATATCGTTTCCAGGGCGGTGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAT

>NZ_CP036262|10|8|2304044-2304137|CRISPRCasFinder
GGCCGGACGGCTCGCGCCGTTCCGCTAAGAAT	GCGTACCGCCAATATCGTTTCCAGGGCGGT
GGCCGGACGGCTTGCGCCGTTCCGCTAAGAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145351181.1\|2308131_2310432_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377775
NZ_CP036262.1\|WP_145351186.1\|2318816_2319014_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351180.1\|2306322_2307942_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP036262.1\|WP_145351168.1\|2290187_2293019_-\|leucine--tRNA-ligase	unknown	unknown	gnl\|CDD\|178177
NZ_CP036262.1\|WP_145351169.1\|2293313_2294114_+\|type-I-methionyl-aminopeptidase	unknown	unknown	gnl\|CDD\|235576
NZ_CP036262.1\|WP_145351171.1\|2296286_2297837_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351178.1\|2304156_2305128_-\|serine-acetyltransferase	unknown	unknown	gnl\|CDD\|200082
NZ_CP036262.1\|WP_145351179.1\|2305966_2306326_-\|response-regulator	unknown	unknown	gnl\|CDD\|381091
NZ_CP036262.1\|WP_145351173.1\|2299139_2300630_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	unknown	unknown	gnl\|CDD\|235489
NZ_CP036262.1\|WP_145351174.1\|2300626_2302114_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	unknown	unknown	gnl\|CDD\|234572
NZ_CP036262.1\|WP_145351184.1\|2313492_2314077_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351170.1\|2294343_2295861_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377874
NZ_CP036262.1\|WP_145351183.1\|2312993_2313491_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351172.1\|2297833_2298421_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239773
NZ_CP036262.1\|WP_145351175.1\|2302124_2302418_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	unknown	unknown	gnl\|CDD\|178810
NZ_CP036262.1\|WP_145351177.1\|2302980_2303511_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351176.1\|2302450_2302729_-\|50S-ribosomal-protein-L28	unknown	unknown	gnl\|CDD\|234736
NZ_CP036262.1\|WP_145355129.1\|2305230_2305491_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351185.1\|2314277_2318198_-\|MMPL-family-transporter	unknown	unknown	gnl\|CDD\|223964
NZ_CP036262.1\|WP_145351182.1\|2310431_2312966_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131281

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145351181.1\|2308131_2310432_-\|hypothetical-protein	gnl\|CDD\|377775	pfam07090, GATase1_like, Putative glutamine amidotransferase. This family consists of several hypothetical bacterial proteins of around 250 residues in length. The function of this family is unknown. The structure of this cytoplasmic domain was solved by the Midwest Center for Structural Genomics (MCSG). The structure has been classified as part of the Class-I Glutamine amidotransferase superfamily owing to similarity with other known structures. The monomer combines with itself to form a hexamer, and this hexamer exposes a potential catalytic surface rich in Glu, Asp, Tyr, Ser.Trp and His residues.	5.12129e-16
NZ_CP036262.1\|WP_145351168.1\|2290187_2293019_-\|leucine--tRNA-ligase	gnl\|CDD\|178177	PLN02563, PLN02563, aminoacyl-tRNA ligase.	0
NZ_CP036262.1\|WP_145351180.1\|2306322_2307942_-\|GAF-domain-containing-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	1.01804e-45
NZ_CP036262.1\|WP_145351178.1\|2304156_2305128_-\|serine-acetyltransferase	gnl\|CDD\|200082	TIGR01172, Serine_acetyltransferase, serine O-acetyltransferase. Cysteine biosynthesis [Amino acid biosynthesis, Serine family].	4.545e-53
NZ_CP036262.1\|WP_145351179.1\|2305966_2306326_-\|response-regulator	gnl\|CDD\|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.11223e-30
NZ_CP036262.1\|WP_145351173.1\|2299139_2300630_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB	gnl\|CDD\|235489	PRK05477, gatB, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB.	0
NZ_CP036262.1\|WP_145351174.1\|2300626_2302114_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA	gnl\|CDD\|234572	PRK00012, gatA, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA.	0
NZ_CP036262.1\|WP_145351170.1\|2294343_2295861_-\|hypothetical-protein	gnl\|CDD\|377874	pfam07585, BBP7, Putative beta barrel porin-7 (BBP7). This is a family of putative beta barrel porin-7 BBP7 proteins identified initially in Rhodopirellula baltica.	3.02164e-06
NZ_CP036262.1\|WP_145351172.1\|2297833_2298421_+\|hypothetical-protein	gnl\|CDD\|239773	cd04240, AAK_UC, AAK_UC: Uncharacterized (UC) amino acid kinase-like proteins found mainly in archaea and a few bacteria. Sequences in this CD are members of the Amino Acid Kinase (AAK) superfamily.	2.99324e-10
NZ_CP036262.1\|WP_145351175.1\|2302124_2302418_-\|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC	gnl\|CDD\|178810	PRK00034, gatC, Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC.	4.00932e-33
NZ_CP036262.1\|WP_145351176.1\|2302450_2302729_-\|50S-ribosomal-protein-L28	gnl\|CDD\|234736	PRK00359, rpmB, 50S ribosomal protein L28; Reviewed.	7.30708e-12
NZ_CP036262.1\|WP_145351169.1\|2293313_2294114_+\|type-I-methionyl-aminopeptidase	gnl\|CDD\|235576	PRK05716, PRK05716, methionine aminopeptidase; Validated.	5.97309e-121
NZ_CP036262.1\|WP_145351185.1\|2314277_2318198_-\|MMPL-family-transporter	gnl\|CDD\|223964	COG1033, COG1033, Predicted exporters of the RND superfamily [General function prediction only].	7.69975e-28
NZ_CP036262.1\|WP_145351182.1\|2310431_2312966_-\|hypothetical-protein	gnl\|CDD\|131281	TIGR02226, hypothetical_protein-transmembrane_prediction, N-terminal double-transmembrane domain. This model represents a prokaryotic N-terminal region of about 80 amino acids. The predicted membrane topology by TMHMM puts the N-terminus outside and spans the membrane twice, with a cytosolic region of about 25 amino acids between the two transmembrane regions. Member proteins tend to be between 600 and 1000 amino acids in length. [Hypothetical proteins, Domain].	2.26671e-18

>NZ_CP036262.1|WP_145351177.1|2302980_2303511_+|hypothetical-protein
MRFHSAFFPISVLAAVLCAGCSLTGSSSTGALSERVQPTEGALVALSAPASEEVFRKIKQAKAQNSIVLQVAGDDEPVRVLPLPPEGQTVHVSTLLDQTGVRSAIKHMRVRVYRSETGDWNCPPMEVAFDGKQVRPENDYALHPGDRIEVQADKTGVLDNFIGSLIPLNTRRALGG
>NZ_CP036262.1|WP_145351176.1|2302450_2302729_-|50S-ribosomal-protein-L28
MARQCEACGKKVQMGNRVETRGKAKYLGGVGTKITGITRRKFVPNLQKVHITTPSGENKSVRVCTSCIRSGAVRKKVHVKPFELGDKKPAKK
>NZ_CP036262.1|WP_145351175.1|2302124_2302418_-|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatC
MAFSDDDIRKVAHLARLELTDQEVQRLGPQLERILGFVEQLAELNTDEVEPMTTALDVSNRWMADEPAPSLSREAALANAPLADDECFLVPPVLPPS
>NZ_CP036262.1|WP_145351174.1|2300626_2302114_-|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatA
MTIPLDSAARLQQMLQSREVSAAEVAQATLDRTATTEPTVSAFTHLATESLLAQAADIDRRRVAGESLGPLAGIPIAIKDVLCTADMPTTCSSKMLKDFHPPYDATVVAKLRSADALLVGKTNMDEFAMGASTENSAFGVTRNPWDLTRTPGGSSGGAAAVVAAQNVPLSLGSDTGGSIRQPAAFCGVTGLKPTYGRVSRFGLVAFASSLDQVGPLGWDVADTALLLDHIAGFDPRDSTSLDAPVEDYSAAAAKPDVKGMRIGVMRGQLDDPGLDPDARSAVAAAIDVYRDAGATLVDVEFAHSKYWVPTYYIIAPCEASSNLSRYDGAHYGHRAEIDEAAAKKDGPLVATYCKSRSEGFGDEVKRRIMLGTYALSEGYSAKYYAKSLRVRRLIRGDYDAAFEKVDALLSPVTPSAAFPLGDKMEDPLQMYLCDLFTVGANLAGIPALSLPAGTTESGLPLGVQLQAPPLKESTLFRAGAMFQQATTHHRRRPVA
>NZ_CP036262.1|WP_145351173.1|2299139_2300630_-|Asp-tRNA(Asn)/Glu-tRNA(Gln)-amidotransferase-subunit-GatB
MSERLDDGRFPHKIVIGLEVHAQLKTQTKLFCRCSAQFGAAPNTQVCPVCLGLPGALPVLNEEAISLAIVTGLALNCTIPPLTKWDRKQYFYPDLPKGYQISQFDLPICAEGYLDITDPENDEETRRIGLFRAHLEEDAGKSMHDETSGRDFTRIDLNRCGTPLLEIVSKPELRSAAEAKNYLTELRLLLRHLKVSDCEMQEGSLRVDANVNLHIDKDNQRIATPIVEVKNMNSFRAVERAIEFEAIRQYQEWEDTGITIETMGKRTFGWNDATETTFVQREKEESADYRYFPDPDLLPVQIPKEQVEAVRQAMGELPAETRERFQTQHGLAPYDADVLVNQGPAMVGFFETAAGIAKAPKRVSSWIQQDVMRTLKEQQIDLEDFPIQAETLGELLGEVQAGKLDNNRARDVFQHLLANGGTVAEATKSLGIEAVDDNELDTICDQLLAANPQVIEDVQGGKPQAIGSLIGQAKKINPNINPGQLRQTLLQKIAEA
>NZ_CP036262.1|WP_145351172.1|2297833_2298421_+|hypothetical-protein
MKQAVVHRRVIKLGGSLLAAPDLVSRIQSWLNRQPKANENLWIIGGGEIVEGLRVYDQIHLLDPVAMHWRCVRQMRSTFEILAELFPAWTQITSEAEFSAACSRGRFAPQTLIAADTFFTPANDGHLPADWTTTSDSIAAFLAQQTDAEELVLLKSCEISAQATIAELVANGTIDQAFLFASKGLPLVRAEALEG
>NZ_CP036262.1|WP_145351171.1|2296286_2297837_+|hypothetical-protein
MTANFESIAQLMERLGPPPQAIMDDWIAQLTAGSSFHEEATDGDFGLRDVATRYAVDRQNRLVRMEDSPQSSASGNLWQSPDAVNESREVVVTTARSPAGRVRANRGRRVARFRRGAIPLAGLGCVGALVGWGIFAKSSGTSGSDVVEKSKPAEKSKPVAQAMPNVLDANARLHSSQGRGDAFSLFKPEPEGFVLGDQGEQELEEIDHDNGDGLAVSGAKPVVSLQGIPERLQPAAMVDAAVEELRQEDYDALPGQEVRTANQADSEAPATGDSPVHPSSPQLEIDPLVFEFYEHDQRKAWHLGTAPPAERTQLGFSFVLPADIDLIWVMPPENDSQRASMFVVQLTSADNREVAIQLRYDLRIAKRLTCRRRLYARLDPQLPWFPLEAPKFSEWMHQQFFQQKQQGILLAAMERRYADADSSTRRQLRPQRDALRQSIEQVESVLERSSQLSHLLDSLAAPASMDLRLQVRSPEKNEILLSSRGADFLPERDLPDGYHVVRFEEEPRDVPRENPK
>NZ_CP036262.1|WP_145351170.1|2294343_2295861_-|hypothetical-protein
MPKIIQWSRTVLTLAATLAVATFAVAAPPMPPAADADYGASGYLTPRGMPPVGTPGVMPAMYSAMPGPPMGVMQAGGMGMPGGQGVSPAGFNGSSGCDASGCDCLGYGCNRCSSGPVGSGGILDRMRGGGPGMMGQGPMGYGMMGHGGGCGCGSCGGMGLLGNGRLRHGHIAGLLGMLMPYGEAGPNAPRWFDFSAEATFLKRNTQNPSSLLSTFGAAGTPALYSSAADLEDIEAGIRLSGAIILGVGSNLELTYMGGNKWEDSSAVNATTAPPLNLFSFISFYGTNPVGGYADSDNASRQGISGEANFHSGEINYRQRTAGATGRLQGSWLAGLRYIRLDEALTFTSTGNVGGTPRYLNLTNSTKNDLFGVQIGGDLWWNLMAGVSIGSELKLGVLENDVNRNIYATGSNIGAGATAGSRGDFIGSSETTGMLELNTAIVYRLSHSWAFRSSYYILAVDEIGGGMNLTESRNLLLTPQVSNANAPVSYDPLVLQGFTFGAEYTW
>NZ_CP036262.1|WP_145351169.1|2293313_2294114_+|type-I-methionyl-aminopeptidase
MLRKRNKLQLTAAQRDSMRKAGRFNADLLDYLRPFITAGVTTGSIDDRVCEYTQKHGHRAATLGYQGYPKSCCTSINDVICHGIPNEYVLQDGDIVNVDLTSVVDGWFGDQSETFLIGEVSDEARAVTQCSFDCLYMAIEALEPGCPVSVIGETVVREAQARGFSVVREYVGHGLGRAFHQDPSIPHFPNRQSRIDRLLPGICFTVEPMINAGTRYAKPVDKADGWTVRTKDGKLSAQFEHSVLMTETGPEILTLTQDGPRRGHRF
>NZ_CP036262.1|WP_145351168.1|2290187_2293019_-|leucine--tRNA-ligase
MPRYTPSEIEPRWQAYWEQNRTFATPESPGPTKRYVLDMFPYPSGEGLHVGHPEGYTATDIVSRFARMKGETVLHPMGFDAFGLPAEEHAIKTGEHPRIQTEKNIAEFTRQLKMLGFSYDWDRAIATTDPGYVRWTQWIFTVLYDTWFDPEQNKGRPISELPIPAEIAAAGETAIETYQAEFRLAYETEAPVNWCDALGTVLANEEVIDGKSERGGHPVRRLPLRQWMLRITAYAERLLSGLENLDWPGGIKTLQQDWIGRSTGAEVDFFIGKETDFADWKKSRAGKPMPTELAEDALRVYTTRPDTLFGATYMVVAPEHPAVDRLTTPAAAADVQKYRDAAAFKSERERTQGEREKTGVFTGSFAINPVNGKPVPIWIADYVMASYGTGAIMAVPAHDERDFEFARQFALPVIAVVDPPADLENREDILAGKACFAGTGLAINSGSFDGQETTQVKATVTQDLETAGLGKSAINYKLRDWLFSRQRFWGEPFPVLHEIDSDGKDTGRKRTVPTGDLPVQLPELADFRPHGRPEPMLEKADQSWLQVELDGKRYRRETNTMPQWAGSCWYFLRYIDPTNDTCLIDPDKERAWMPVDLYVGGAEHAVLHLLYSRFWHKVLFDRGHVHCDEPFQKLINQGMILGEAELTVFQTEAGAYVSPADVRRSEEGPTAPDGSPVHPVSVQDTDVEKQGDNLVLAAEPEIRVESRSFKMSKSRGNVVNPDVVVKEYGADSLRLYEMFMGPLEATKPWSMAGVGGVRNFLDRSWRMIVDKDAEQIELSAAITDKECTEAQNRQLHKTIRSVSEDIESLSFNTAIARMMEFVNFFTREKQRPRAAMQSFVLLLSPFAPHIAEELWEILGNKKTLAYEAWPEWDEAALIETTVEIPVQINGKVRTKLVVAADIKKEDLQAQVMELEKIQEATAGKQIVKTIVVPGRLVNIVVKG
>NZ_CP036262.1|WP_145351178.1|2304156_2305128_-|serine-acetyltransferase
MASDFRLKQQLPDLTEKIVETYTPDDVINHLGHCPLPSYEAVIEILSDLKDILYPGYRRKVGLHSGNIQYHVGGLIDQLHDSLTTQIARALRHDDRVRNSHNDCESDIDFEAKGQAMAIELLRRIPELRKVLSTDVQAAFDGDPACHTTDEIVFCYPGFEAITVFRIAHELLQLGVPFIPRMMTEWAHKTTGIDIHPGATVGNHFFIDHGTGVVIGETCEIGAHVKLYQGVTLGALSFPTDADGQLIRGTKRHPTIEDRVVVYANATILGGRTVVGHDSVIGSSVWITKTVSPYTTVTLEKPQLRVRGAASAESHDPELNFQI
>NZ_CP036262.1|WP_145355129.1|2305230_2305491_-|hypothetical-protein
MLSRLGGRNECQSCQSGVAVGCRPGPLRWQQGGLNYSEGLATGHMAQGSNTRPANPGPASGTVAYPYYTTRGPRDFLLDNPPTIGN
>NZ_CP036262.1|WP_145351179.1|2305966_2306326_-|response-regulator
MTPPLRIVIADDEQDIRHGLHRLLAKLAYEVVGEASNGHELLSCCRETTPDVVITDIRMPIMSGIEAANELSKTHSIPIIVVSAHERPQTQTECISDFLLKPVSLTSLQAAIIRACPQA
>NZ_CP036262.1|WP_145351180.1|2306322_2307942_-|GAF-domain-containing-protein
MNDNRNLLARDLQGQTRVLKRLAKGDSLEDILQTLVEVAEESRPEMIASILLVDRETGCLRMGAARQLPKFYMDACEGLMPGPSVGSCGTAAYTGKRVIVTDIDTDPLWSGVREFAQRASLRACWSEPIIGSTGEVLGTLAMYYKTPRAPEQSELEFVSSSANLAALAIERVRHQREVEGERALLKTIVGGIPDALISSSLDRKITHYNASAAQLFGYAATEAMGMPTLELYANSDDYHRLGSFPFKAAHAPVLAATEVEWKKKSGETFPGEIVATTIRDEQGKSLGYLGLIRDITDRKAAEAKLAESQRKLVQAERLAAMGEMVSAIAHESRNALQRIQVCVDILQYEMAEDAEARDDLDRISHATTDLQRLHEELCNYAGPIQLDISQGDLSEVWQKAWKNLQVSRTDRDARLCEQIDTVDLKCPMDAFRIEQVFRNLFENSLAACEDPVRICISCRNVEVDGVPSLSIQVRDNGPGLPEEIRPLVFEAFHTTKAKGTGLGMAVAKRFLEAHKGSIAIGNDHGDGAEFVMTLPRELE
>NZ_CP036262.1|WP_145351181.1|2308131_2310432_-|hypothetical-protein
MQITWNPTFGSIWLVVLAFVIVFLLLYLVRPQQDGLTPSRQRWLLGLRSGGALILLLAMLRPTMVRTTETPVPATLAVLLDGSSSMSLPSGDGRDRWTVQSEVWSKLLPSLQGRDEMLDVQVFQYAQKASPLTMEAVSDWLSTQPTGRETDLSIPLQSAVSQASGRPLAGVVMVGDGTQTSRAQGGGAQQSARLLAALEVPLWTVPIGQRRGDETERDVEITDVPESLRLFSGNSFKLPVTIRTQSLAGADIPVRVRWVPQALDASGQPSAPIENETSIRSVVPRTQSDSQAMEFSLEAPAPGRYQLEVSADNQAGEALTINNQQIAFVDVREGGGRILYLEGEPREEQLRLRLALRRFPDLELVYQWIRRDTESTWPVDLSAALQPDQFDIYILGDLHAKALGNDQLELLQKRVAEGAGLMMLGGLNTYDEGGYGQSPLAEVLPIQLSPEAARPVDSPPSPEMQIQGPVPLRVVRNHPLVQIGDANRPQATFDQLPPLTGANRFTGIKAIPGVQVLLESDQKDPLLVVGEYGNGRVVTFAGDSTWQWWRKGASLQHRRFWRQIMLWLMARDTLSDDAIAIELEGRRFAVDATPSFTVRARFSQSKTLETPLTAELVDSAGTVTSLPVIRQPAADGEAIVSGKLSNLSPGIYRMRASASGEDSPLKPDEIAFQVIDNDREKLRPIADPAFLEQLADLTGEAGGKAFAVDELDQLIDAINRRRSDAALPITKQYRLGNDPGTGWLLFLLFAGCLGTDWALRRRWGLA
>NZ_CP036262.1|WP_145351182.1|2310431_2312966_-|hypothetical-protein
MSFLNATLIFGALAAAIPIVLHLIAKKQPQRMLFPAVRFLSERVEVQRSKLRIRRWLLLALRAALLAILALALAQPQIHASAGGTWLTIAIAFLFGLALLALAATAISRQMTRSLVLGLTAAGLALLILAIGWSGFVWAGTAPVQALDSSPAAVAIVIDNSPRSGYLIENKTRLDKLKSTARWLVTRYPADSRITIMDRSARPASYSLDTAAAVRGIDKLDPLQNVQPLADRIEAAVRLVRSSELERKAVFVLSDLSEQSWFPSGKDDPETAESPLLRLLSEAPPVRLQILPVDFQRDGRESPPTTPPQNRRLGLPRLSDTSPPQQVSVPLQIVVTSEPDTPASEVRCEAQLYALDPTLPAVRDGQTVLPKLQTVDRTSVQLAGGESAEMILTLPPLPIGTHHGQIHLLGNDPLAIDDTRFFSLVVRPPAKLLIASSDTAAADHLEKLLNADFGPGDPRAEFVVQRTRGTKWTAAQLQAVDAVALLDPNPDQVSETDANSLLKWVSEGGSLFVALGGSSRGSLVTTEPSTAPTASSDEEAIVDDQRPPRRRLFPLKRIWRVPEPGTFLEIIRPDHPVMQELSAIPGGVPWAPFRIHRYWQLATDPSDSVLARYAGTSNGAVIERAFGSGRMILMTTPLAPSYQHPQADWNELSSAGSAWPSFLMLRQIFSYLGNRDEPGLNVQVGDAVALAVGVRDAESENQDASEDLRRLQMFSADSPPVPVPVTSGLATVGTTSNGGNYWLRGIQPAIGFSVNLSPEATNLKSIEPADLEALLGAENFDFISDAESIRESEGGGRDLRPLYSQAMLLVLGLFLFEQILANRFYRTGNSRPALSTRLRSSGAA
>NZ_CP036262.1|WP_145351183.1|2312993_2313491_-|hypothetical-protein
MNEPIEPHAVDPLTAAVSSPPTDRVASLDHVTKDRNVELAKSLARWQRFVAMIIIGLAILVLGNYVVVFATGEAAGIVPFLFSFAISAISVIVIYVLPSVFLWRAAGASRQFANQPNSNSWAQLIYQQAKFWQVTGIIVLVCFGMMIGLMGLMLLLTIVGFSSFP
>NZ_CP036262.1|WP_145351184.1|2313492_2314077_-|hypothetical-protein
MTDLNPSNQNPYAAATGNISLHSDVAATVNTPQTDARRLGFWQFFLGIILLAIFGIVVLILGLQMLLAGVLAGSIAGVIGVGLVILIMAFFYLLPAISIMRAGATAKQYSVTPDAVQQTLLLERQLRTWRVLGSLALLGVVFSFSALALTVGRTVTSSPPGALGPAVRDVTVPVESDSLQPSQPATSLSSEEGT
>NZ_CP036262.1|WP_145351185.1|2314277_2318198_-|MMPL-family-transporter
MKQSFLSKRSPFGISNALVILLVIFFFVPWAIRSARMSLQHTENNVKDWLPSEFRETSELAWFGKYFAGERFILATWPGCTEDDQRLQLFAQKLRSEAEGSTPAVLPANWEAAKETAAKLQLMLPSDHHKNWGGLDEKWLVSATGRWYYLTPDGKLYRWDVESNAVHSSWIAFQRATGSYKLDGTFVAAFGGPPGKRVANPYYNDPALLSAPLFRSVQTGPDVASLLAVEGGPLWPVDLTDPELKPQIARRHAIDRLTGTLYAPAVPHEFDWTAEGFARVVEEYRDSKSEESDDIASAEAASEVATDSSKPLPAELVEAFDLALQQFTQARYQGDREALLNADTKQHDEAWYAVFDAVEIKPPPRQTCVMVTLTPLGEQKLPYVVGRGVMGGPRGRLLTLAEQSGLEAAAIPSSAPPPFNVVEAVGSSGRPPLRLGGPPVDNVTIDEEGTITLSRLVGYSVLLGFGLSYLCFRSLKVTIMIFAVGGMSAVFGMAMVGWTGTAVDAILLSMPSLVYVLGLSGAIHVVNYYRDEVESEGPAGAAGRAFRHALVPCTLAAVTTAIGLMSLYTSNITPIRKFGFFSALGVLATVIILFAYLPAALETFIPHLAKKRQTKKKSIGDGGVLGRAWGAVGDFIVKRHWWVSTAATALLIFCLLGLFKIQTTVQLLKLFSADSRIINDYAWLEDNFGKLVPMELVVRLPESPDAEVAAAEPAEDTRSSWNQTASNAATTSADPEMSMLEKVEAVSRIQHVVEQALGETGLGIVGQAMSTATFLPDLPPPSNGAIKSERYLFNQELTVGRNDLKGSDYFRVEENGPFAGSDLFRISLRVSALSDVDYGRFIYQLRETVEPVLEAYRSEEQIKQRMPTRSRGVRKIVVLGRGAPEHLGVEPVLQPKPEMTPEERKASETLAQRTLRFLEGTPPATDSRVIDQRSIYETTLAELLRNHSSTRVLWHDPSDGKLDGKETHEQWGKNLESADMIIMLRDHEDYDLSFIEQHAKNWIDVRQIPFDRTIPTVVDEIPVAENAGPVEVVYTGVVPVVYKAQRTLLHSLVESIGWAFVLIAGVMTILLNPGRMPFTWFAPSNLGFGFAAGCVAMIPNIFPVAVVFGTMCHMGIKIDIGTMMTASVAMGVAVDDTIHFLSWFRHNLDTGMERIEAIKATYRRVGPAMTQTTIVGGLGLFVFALSSFTPTQQFGTLMLVMLAAALVGDLIFLPALLAGPLGRLFKARPPKPTANLTAPISEQDPPEFDSTSNENGRSSGSGPHSAESQPQSQTRSSVPPPASLRTRGLRTDQPHQYDPSSDPGPH
>NZ_CP036262.1|WP_145351186.1|2318816_2319014_+|hypothetical-protein
MSSIPAPVRQVLQARSDATLQKIDMAVLAKHLDVQQQAGDSVNELLQQNATIQRQLAAGYLDVRV

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Crispr_ID: NZ_CP036262_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_11

2949071-2949235

Orphan

Consensus_repeat	Method
ATCTACTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCAATCGCATCGAAAGCAGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_11

>merge|NZ_CP036262|11|2949071-2949235|CRISPRCasFinder
ATCTACTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCAATCGCATCGAAAGCAGAGTGAATTTGCCGGTCGGCTTGTGTTAATCCGCTGGGAGATTCGTCTGCAGATGGTATCTACTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCAATCGCATTGAAAGCAGA

>NZ_CP036262|11|9|2949071-2949235|CRISPRCasFinder
ATCTACTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCAATCGCATCGAAAGCAGA	GTGAATTTGCCGGTCGGCTTGTGTTAATCCGCTGGGAGATTCGTCTGCAGATGGT
ATCTACTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCAATCGCATTGAAAGCAGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145351666.1\|2935734_2936784_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP036262.1\|WP_145351675.1\|2952163_2953666_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351665.1\|2935301_2935712_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351680.1\|2958616_2959102_-\|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl\|CDD\|181730
NZ_CP036262.1\|WP_145351674.1\|2951539_2952124_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351667.1\|2937443_2938787_-\|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	unknown	unknown	gnl\|CDD\|236307
NZ_CP036262.1\|WP_145351668.1\|2939438_2940536_-\|M24-family-metallopeptidase	unknown	unknown	gnl\|CDD\|238525
NZ_CP036262.1\|WP_145355216.1\|2949445_2950723_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351678.1\|2956609_2957383_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351669.1\|2940893_2944355_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036262.1\|WP_145351673.1\|2951050_2951488_+\|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|273242
NZ_CP036262.1\|WP_145351679.1\|2957639_2958587_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|350353
NZ_CP036262.1\|WP_145351670.1\|2944803_2944977_-\|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS	unknown	unknown	gnl\|CDD\|377073
NZ_CP036262.1\|WP_145351676.1\|2954431_2955967_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145351672.1\|2948405_2948954_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377555
NZ_CP036262.1\|WP_145351677.1\|2956085_2956490_+\|holo-[acyl-carrier-protein]-synthase	unknown	unknown	gnl\|CDD\|223807
NZ_CP036262.1\|WP_145355211.1\|2938886_2939363_-\|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl\|CDD\|235777
NZ_CP036262.1\|WP_145351671.1\|2947535_2948372_-\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|372587
NZ_CP036262.1\|WP_145355213.1\|2944983_2947482_-\|heavy-metal-translocating-P-type-ATPase	unknown	unknown	gnl\|CDD\|319851
NZ_CP036262.1\|WP_145351681.1\|2959007_2960453_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145351666.1\|2935734_2936784_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	2.32852e-72
NZ_CP036262.1\|WP_145351667.1\|2937443_2938787_-\|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	gnl\|CDD\|236307	PRK08591, PRK08591, acetyl-CoA carboxylase biotin carboxylase subunit; Validated.	0
NZ_CP036262.1\|WP_145351668.1\|2939438_2940536_-\|M24-family-metallopeptidase	gnl\|CDD\|238525	cd01092, APP-like, Similar to Prolidase and Aminopeptidase P. The members of this subfamily presumably catalyse hydrolysis of Xaa-Pro dipeptides and/or release of any N-terminal amino acid, including proline, that is linked with proline.	3.96462e-109
NZ_CP036262.1\|WP_145355213.1\|2944983_2947482_-\|heavy-metal-translocating-P-type-ATPase	gnl\|CDD\|319851	cd07553, P-type_ATPase_HM, P-type heavy metal-transporting ATPase; uncharacterized subfamily. Uncharacterized subfamily of the heavy metal-transporting ATPases (Type IB ATPases) which transport heavy metal ions (Cu(+), Cu(2+), Zn(2+), Cd(2+), Co(2+), etc.) across biological membranes. The characteristic N-terminal heavy metal associated (HMA) domain of this group is essential for the binding of metal ions. This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP036262.1\|WP_145351669.1\|2940893_2944355_+\|hypothetical-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	0.00016421
NZ_CP036262.1\|WP_145351677.1\|2956085_2956490_+\|holo-[acyl-carrier-protein]-synthase	gnl\|CDD\|223807	COG0736, AcpS, Phosphopantetheinyl transferase (holo-ACP synthase) [Lipid metabolism].	6.27074e-38
NZ_CP036262.1\|WP_145351679.1\|2957639_2958587_-\|hypothetical-protein	gnl\|CDD\|350353	cd14503, PTP-bact, bacterial tyrosine-protein phosphataseS similar to Neisseria NMA1982. This subfamily is composed of bacterial tyrosine-protein phosphatases similar to Neisseria meningitidis NMA1982, which displays phosphatase activity but whose biological function is still unknown.	3.11973e-13
NZ_CP036262.1\|WP_145351670.1\|2944803_2944977_-\|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS	gnl\|CDD\|377073	pfam03597, FixS, Cytochrome oxidase maturation protein cbb3-type.	1.97974e-17
NZ_CP036262.1\|WP_145351676.1\|2954431_2955967_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	4.88626e-29
NZ_CP036262.1\|WP_145351672.1\|2948405_2948954_-\|hypothetical-protein	gnl\|CDD\|377555	pfam05751, FixH, FixH. This family consists of several Rhizobium FixH like proteins. It has been suggested that suggested that the four proteins FixG, FixH, FixI, and FixS may participate in a membrane-bound complex coupling the FixI cation pump with a redox process catalyzed by FixG.	4.31401e-18
NZ_CP036262.1\|WP_145351680.1\|2958616_2959102_-\|aminoacyl-tRNA-hydrolase	gnl\|CDD\|181730	PRK09256, PRK09256, aminoacyl-tRNA hydrolase.	4.01358e-49
NZ_CP036262.1\|WP_145351673.1\|2951050_2951488_+\|Rrf2-family-transcriptional-regulator	gnl\|CDD\|273242	TIGR00738, Putative_HTH-type_transcriptional_regulator, Rrf2 family protein. This model represents a superfamily of probable transcriptional regulators. One member, RRF2 of Desulfovibrio vulgaris is an apparent regulatory protein experimentally (MEDLINE:97293189). The N-terminal region appears related to the DNA-binding biotin repressor region of the BirA bifunctional according to results after three rounds of PSI-BLAST with a fairly high stringency. [Unknown function, General].	1.31737e-35
NZ_CP036262.1\|WP_145351671.1\|2947535_2948372_-\|sulfite-exporter-TauE/SafE-family-protein	gnl\|CDD\|372587	pfam13386, DsbD_2, Cytochrome C biogenesis protein transmembrane region.	6.4075e-34
NZ_CP036262.1\|WP_145355211.1\|2938886_2939363_-\|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl\|CDD\|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	1.1891e-52
NZ_CP036262.1\|WP_145351681.1\|2959007_2960453_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	2.8001e-12

>NZ_CP036262.1|WP_145351672.1|2948405_2948954_-|hypothetical-protein
MPPSSASSDPASAGPREKASPAEERKARRFWVSFIVMLMCIPVITGGSAIYLSKTRSLISVIPDYYQASLHWDETQQERSAAERLGWTVKLQPAEIADGQGMRALELWVHDAQKNPVDDLQIEGHFFRHRDANGRLPVQLRGVGEGHYLALEPMRETGIWQFELTIDGAPEPMAVSSTMNVQ
>NZ_CP036262.1|WP_145351671.1|2947535_2948372_-|sulfite-exporter-TauE/SafE-family-protein
MWILLAAVLTASVLGSMHCVGMCGPLAIWASGAGERQPRKTVFASTSLYHFGRLLTYTLVGFAAGAIGSFVDWTGDAVGFQIAAARTVGGVMIVLGVFKLRALLVPPPMPTDGHSPPASKIGGLLVRLRPYIFQLPIPLRAVVTGLLTTLLPCGWLYMFALFAAGTGSPVTGGLVMAAFWLGSVPALVGLVAGTQVLARRFTRLVPIAASLLLILTGCFTTSGRGFANLQSLTAFQNTVQSDRLDGESDPAALLQRVRTVGDAPLPCCEDLSIETEPS
>NZ_CP036262.1|WP_145355213.1|2944983_2947482_-|heavy-metal-translocating-P-type-ATPase
MVPDSATPDKSAPESKSDSRTPSKVSREAPCTHCDLPTPYVGENPPHPLFCCNGCRGAYELIQGWGLDSYYDLRDQANGERNRMPEATDKGRFDSFDDPEFLGLSTPKQQSDGLQSAQLAVHGLHCAACAWLIENAAQQTEGWNTARVHLGDHTLRVMFDPATCSLSGIARLLHRLGYELAPITKQPDAHFRKENRRLLTQIAIAGFCAANAMWIAVALYAGDASGVAAEHRLLLRLMGTGLGLIAVAVPGRTFFRGAFAALRTWTPHMDLPVALGLSVGTVTGTVNAISGRGDVYFDSLAVLVFFLLVGRWIQFHQQHRAAKAVDLLLRITPAHANRIAADNTTDWVLVDTLRPDDQIRVAAGESLPADGIIAAGNTTLDRSLLTGESQPVAAQTGDEVSAGTLNLSRSIDVTVRAVGSESRIGRVMQSVESAMAERTPIVQLADAIGGWFVVIVTLLAIAALVIWSGEGWGLAAGHATALLIVACPCALALATPLAIAVSLGRAAKRKILIRDGASLQLLASKGILWFDKTGTLTEGRSRAQVLYGPETALSDAAAVERDCSHPIASAIERECLLQGLTPPDDAELLVVETGGVQGVCEGRQIVVGNIPFLTSKGIVCSAEILAAVDASLQIAATPIVIAVDGVATTVLGLSDPLRQQAAETVATLQRRGWQVGILSGDHPAIVAAVAQQIGIPLELAHGGLLPADKLERVRQPQSMITVMIGDGANDAAALAAADVGIAVRGGAEVSLQAAPIFIASGRLTSIVELIRGSSATSKLIRTTFAVSLSYNLFAVGFALAGWISPLLAAVLMPLSSISVLSLTLAWPTFRSP
>NZ_CP036262.1|WP_145351670.1|2944803_2944977_-|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS
MSVLYIALPIAIFLGAAGMVACIRCIRSGQYDDMDTPAVRMLIDDKPSVEKKQTKDK
>NZ_CP036262.1|WP_145351669.1|2940893_2944355_+|hypothetical-protein
MTVSTDPFAVSNHPVPAMPTPPARGLGGLFIVLSVIAAISLALCCGMGTLAYFSMQQFLVGEVAASLPERQNSFADDSARFEQSLASLPEKPSPDPSLQKFVASAIATLQEEGEPPFSTDMFLEAVRQSEHSGGNLSMANRIQIRHWLNLYQPQPDVAPLSRILQFHLSEEGRLASVDLLFYSDENQAESHQWFLVKESNQWRLYDWQRLEYGRRLSDEYASYALGTAPVSDGYDEMLIKLVDLEEESRQGVTPQLIDKLRRLERKPMLAADRSIGMLRIAYQWLAWGESKEAIRLLKSIPDPQQRWGVYPVLAMSYLGVDEIDKALATAKLAAQQAPHHPNVYWLYSEIYDRMDRPDESAEAAIKALDICPQDGGLFQTLLAQDRDQDIPRLLTFAIDNPSEDYWTQLLNQASYSREWGLALVEAMSARDDLPVGLEHLAKGNVAWADEDYRLAGDEFFQATETVVLPELLAIANNDHLLARVESEDYQQLFAESKDRGEMAKRLLEWCLDGEFYSDSLPLIAALQGIPETQDPWVRGLKGWAFHAAGQFEPAVAELTAFADWANADGSLSEEDAWYAASSDYYLADSFLNLQRPLEVIERWPNDKNRHQQIGDHLVKVYDLRQLQDFVTQVDEDSVTSVRLQEIRIEAEIAMRMADPEACRVAHAKALNLASIVFDDEDSYELASMVRGHARDLIWLQDYSDTRILQRYLKTPFVKPFLNQLVWQGGDVLDLKALIYVPQLSRQVPVVEWNEVQGEVDFELGKYFDAIGDYDQAAKLFQAGLKHVDDSSEWLREQRLLALLGVQIRRQDYDSIAVILEELNQDFDYSIESELVAAMLQGEGKKVLQQIEQADEDSQLAILDWLSDDEATAAMAQAIDQPWMLDLIGKYPLRVIRKSTDANLQLICEERAKIDQEWLDNRLAKALGESYVLKEFPAVDNREDSKSWLLETPSGKRMVFRVRPAEYQSRSLPDSLQIALYGPVQVLMVSVIDVQPNAAQRVFDVCSILAEAEKDVFVCRDVGRSLMWAAPNLPQQLAWKGRVPVGPMVMQNPLLEDVSDVDVESGIDWIDVDKWKEKLNQSGGSLPVVLQVGRGAGEELVSADLIGVDPRDESLLVRPRQASLLVPWIQPAGTYRTGVGFVAVPPEEDDAKAN
>NZ_CP036262.1|WP_145351668.1|2939438_2940536_-|M24-family-metallopeptidase
MNYSARLQEACSRLSSHQVDALFVFNETNVSYLTGFSGDSTVLLLTENGATLLSDRRYETQLQQECPQLPALVRGPDKNMYQLIEEAAASQLADCQSIGFEANHLHWNDYQKLAKSLGARTLVPTSAFIEAQRLIKDEDEIAILRRAVSIAERTFLSIRARLRPDWTELQMAHELESTMRELGASGCGFAPILAIDANAALPHAHPGSQVLNQASTLLVDWGAKFQGYTSDLTRTLSIGPPSDRFHEVYEVVLLAQQTAIEKIRPGIPLKEIDRAARDVIAQAGFGDYFGHGLGHGIGLQVHESPRMASTSEETLESGMVVTVEPGIYLPGEFGVRIEDDVLVTPEGNEVLSSLAKGLDDMIVFL
>NZ_CP036262.1|WP_145355211.1|2938886_2939363_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MNAGGKREAVNVFGIDQLKELIELMEQHDLAEIDLQQDTDRISLKRGGAQPLQAMPAPMAAAPVAAATPAEPAGDGPNILTIKSPMVGTFYTKPNPESENFVKVGAMVSPDTVICIVEAMKVFNEIPAEVSGKVVAVLAENGQPVDFDKPLFKIDTSA
>NZ_CP036262.1|WP_145351667.1|2937443_2938787_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit
MYNRILIANRGEIALRVIRACRELGIESVAVYSQADADSAHVRYADQAFCIGPARSADSYLRIDRIISAAELGDVDAIHPGYGFLAENAHFNEVCRSCKIDFIGPRPEAMEMLGDKNTARSLAIKAEVPVVPGSDGLIDDDNEAIRVANEIGFPVLIKATAGGGGKGMRVAVDQSVLATAVSQARTEAQAAFGNGAVYIEKYIEKPRHIEVQVIADEHGNVVHLYERDCSVQRRHQKLIEEAPSPTLSPEKRTAICEAAVRMIRAANYTNAGTVEFIVDKNDDFYFIEVNARIQVEHPVTEMVTGIDLIKQQILVASGEPLPFKQEDIPCRGVAIECRINAENPDKGFQPNPGKIQHMFAPGGLGVRFDSHVCSGYTVPPYYDSMIGKLIVYQPTRLEAIATMRRALKELAIEGISTTASFHDKVLQHPEFIAGNCDTTFVEREFTN
>NZ_CP036262.1|WP_145351666.1|2935734_2936784_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MNVMEAVMTHPAADFFSTGAVLVSQAMRDVLRIASLAASTDASVLIVGEMGTGKHWLARAIHQASSRRDQPFQRWDCGSIAPLGIGNGEEGLGRSCSPPASGTLFLDHLDRADLPLQDRLSQFVFNAGEQADAHPDSSSTLPAAPCRLIAASSLDLLPPVEEGRFRSDLFWGVNVIPILLPPLRERREDILPLIDHFWKVLNRQIGKQVQSLEGPLLTSLENYPWPGNIDQLFSYLQRVIVCSEGSEPAIDFLPESITGKAKAIAEPVNTADVGSLTTAVVQQGLQTIAEDASDVHSQIVDRVEREVIRQVLLECDGVQTRAASRLGMNRNTLHKKIKDYGMDQPPSAS
>NZ_CP036262.1|WP_145351665.1|2935301_2935712_+|hypothetical-protein
MLSKLPSILAACFVVSSLVFTGCDSDPLGRVEVDGTVTVDGTPLKKGEIMFIPQEPSSPTDSLKIVDGAFKGPVLPGSKQVQIRGYEEVTSDLSADSPEAGVSFNKQILPAKFNDNSELTETIPSSESLKYELSTK
>NZ_CP036262.1|WP_145355216.1|2949445_2950723_-|hypothetical-protein
MGGLFCGLVAHGLTSNDLHAQSASYERPPIDYINAPVSDEVSVLGKQISAGEVELEYDPKFGYLPAVLKALDIPLDSQVLVFSKTSLQLHRIAPGTPRAIYFNDNVYVGYCHRGDALEIAVTDPQQGAIFYTIRQRSSDTPRLLRDRGQCLTCHATNRTQGVPGYLIRSVYSDNSGHPIFSRGTFTTDHASPFIERWGGWYVTGEHGQMRHMGNVTTSDDEAMDYESGANRTTLEGLVDTDPYPSPHSDIVALMVLEHQTQVHNALTFANFETREALHQSYTMNALLERDPDHISESAQRRMTKAVEKLVQQLLLCDEFGLESPVTGTSTFASEFAKRGPTDPSGRSLRDLDLKTRLFRYPCSFLIYSPAFRELPPEVHQRAVSRIQEVLTATEPEEAFAHLSADDRKAILEILVATHADFAERN
>NZ_CP036262.1|WP_145351673.1|2951050_2951488_+|Rrf2-family-transcriptional-regulator
MLSKTAEYALRAVTVLATVQGRPVSADKVAEQTKIPRRYLHKVLQDLTAAGLMSSRPGPGGGYELVGKPETLTILDVVNAVDPIARITSCPLGLTSHTSLCPLHRELDKAYASVENALRKVTLADVVLSTDPIVPLCDIPAIRPK
>NZ_CP036262.1|WP_145351674.1|2951539_2952124_+|hypothetical-protein
MLRMPASRFGFVLTALLTFGFVGAGIPAAFSADAVADEKGTEITIASGAKMMAPATWKVVRPKISIIQNEFAAPGAEPEQTARVTMMAASGSVQANVDRWKGQFQLAAKDGFKEEQKTIEGHTLHLVDLQGTFNERMGGPFAGGRVVHRENYAMAGAILIDPNGGKFFIKMTGPVEAVKANRKAFGEMLDGLKK
>NZ_CP036262.1|WP_145351675.1|2952163_2953666_+|hypothetical-protein
MNIQSFLEHHGVLRNPFAEEDAQTDPVFKEHCIVSAYHPVWDKVYGDPTEPATAIVFGPKGSGKTAMRLQIDRHLAAYNVEHPTKRINVIRYDDFNPFLDHFRERLSRRSAKKPERVLEAWRLWDHMDAILCIGTTQLVDRALEKTGEEEEGPLPVIASRVDDRDLAKLDRTTARDLLLLACCYDQSTSSSFTGRWEQFRRKLGYSNWGVQWDLWLAIGWAVLMLMLTGYLFRTEKIEWDTAAWIFAGLCCLGCFPYARRWFRCQRLAMGIHRHMRVGKREIGSLRKVLLQFPAKELASQPLPRFSRTDDRFELLTKLQLAGKKLGFSGTIVMLDRVDEPHMTGGKPELMRRFVWPLLDNKLLKHPGLGLKLMLPQELHRDIERESTEFHERARLDKQNVIPAFAWTGESLYDLARARMSACAAEGRTPEPKDLFSEQIGYTRLLAVFQSLRVPRHLFRFLYRVLVEHCNKYSDAEPNFQIDSQTFESVLAVYLRDLEPK
>NZ_CP036262.1|WP_145351676.1|2954431_2955967_-|Gfo/Idh/MocA-family-oxidoreductase
MIMEPASMPQRPKLNRRHFVAATTVAAASAAAVRPSLAQSANETMNVAIIGAGGRGGSHVSAFLGNDKTRITHVVDIDPKAASQRAGQIEKEQGKRPEIVTDMRRVFDDASVDAISTATPNHWHALCGVWAMQAGKDCYIEKPICHNIAEGRALVEAAKKYKRICQVGTQSRSSAAVQEAVKFIAEGNIGEVKLARGLCYKRRKSIGPLGDYPIPEGIDFALWTGPATITDPKVTRQRFHYDWHWQRHYGNGDLGNQGPHQTDIARWGLGVDRHPEQIISYGGRLGYRAERKDPTYIDAGDTANTEVSIYDYGDKCLVFETRGLSVDNSADEELNKLFGSTKGNKIGVVFYGTDGYVVQKTYSHCIAYDKDMNVIKEFKGGGDHFGNFVDACNRRDTDVLNADAMTGHLSAGVSHLGNISYYLGEKNKASADQISEAVAKIPSLDDNQATLARTMQHLKDNGVDTNGSPLSLGPLLKFDPEAERFTNNDEANKMLTREYREGFVCPTGDKV
>NZ_CP036262.1|WP_145351677.1|2956085_2956490_+|holo-[acyl-carrier-protein]-synthase
MTIHRLGTHIVECARIANMIAQHGELFLERVYSIGEIEYCGQQGSPHHLYAARWAAKEAVLKVLMTRKTAGIRWTELEVVVDSDGEPRVVLSGRAKKMAEEIGIDEILLTIAHCRTYATATAISLLEDPSSYAD
>NZ_CP036262.1|WP_145351678.1|2956609_2957383_+|hypothetical-protein
MARRLTAAMVAAAAIGGPYVATETEIGKNVSGSVSAMVRTASSTNANRTDNFSDTSTAGPYHAHYQTESLWDQRLGPRTREAMLGSNPLQPSLVGGPVHDLRDVLRFDITPNWISGHFARVTTVLADLQLDGLRVPLVTGTDATDLAGTITYYFDHSGQMQRVNVQGFVGDPADITQLMQQYYHMSPEPTLDAGVFTVRWNGMATGLLKLTRAPVMYSDATHQRYTVFLELNQPNLAYGLSPAAQQIVRADRYTGRW
>NZ_CP036262.1|WP_145351679.1|2957639_2958587_-|hypothetical-protein
MTFTKIIHRTLATGCLVFLLGTSPIVAHPPTSSTESPSSAASATPQPSSREATPLPHWLQWTEQVFSGAQPTTADDFAALQARGIRTIVSVDGARPNVELAKHYGMRYLHVPIGYDGIDPDANLSFFRIAKEVQGTVYVHCHHGKHRGPAAAAVLCMGAGKIDRPQAEANLRSAGTSPNYTGLWKAVRDYRRPAADQELPQLVEIAQVTSTAAWMAQIDRTWDNLKACQNADWKHPKDNPDLVAKHEALQLWEGFTEAQRLLPNDAPTSLKQGLQTSQELSQSLMTALRKNESVKADRLILQLQEACVDCHKVHR
>NZ_CP036262.1|WP_145351680.1|2958616_2959102_-|aminoacyl-tRNA-hydrolase
MQPPRRTLAVVRIAREKDPFVENLVINRRLTIPASQLEVSYARSSGPGGQNVNKVNSKVTLRWQVRDQPLIPDGWRDRFLTAFGTRVTIHGEIVLQSDRYRDAPRNLQDCCDKLQQMLLQVAVPQKARRKTKPTLGSKKRRLDSKKRQSDKKRLRGRPGMD
>NZ_CP036262.1|WP_145351681.1|2959007_2960453_+|PQQ-binding-like-beta-propeller-repeat-protein
MVKRRLITRFSTNGSFSRAMRTTASVRLGGCILMVCLLVDRPGWGQAGSQPNRAEPQNKVSDSDWPQFLGPHGNGHSDATGIRTDWSDGNLKTLWHQPLGTGYGIGSEADGKYYQFDREADQERLRCFDAASGKLIWSESQPVVYRDMYGYNNGPRSSPVIADGSVFTFGVAGQLTCRDEQSGAVSWTVDTNKKYGVIQNFFGVSCSPIVFEDSVIVMVGGSPPEDQQIAMGALDRVSPNGSAIVAFDVKTGEEKWRAGNYLASYSTPLVVELQGEQVLLAFVREGLLAIDPSTGNNRWFHPWRSPRLESVNAALPVVKGNQILISECYDIGSVFLNATTDEAEVVWADNPRSRDKNFRAHWSTPVVIDGALYGCSGRNAPDSDFRCIDFETGTVHWVDRRRTRSSVLAIDGHLVVLDEGGRMQLVKANREALEVVTEIDLGIGAPDRPALQPPCWAAPIYANGRLYVRGRDNVICLQLGK

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_CP036262_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_12

3239666-3239757

Orphan

Consensus_repeat	Method
GAACCGGTGGTTTGCACCACCGGCAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_12

>merge|NZ_CP036262|12|3239666-3239757|CRISPRCasFinder
GAACCGGTGGTTTGCACCACCGGCAACCATCTGCCGCCCTCCGGGCTAATGGCTTGCTTCGGCATTGAACCGGTGGTTTGCACCACCGGCAA

>NZ_CP036262|12|10|3239666-3239757|CRISPRCasFinder
GAACCGGTGGTTTGCACCACCGGCAA	CCATCTGCCGCCCTCCGGGCTAATGGCTTGCTTCGGCATT
GAACCGGTGGTTTGCACCACCGGCAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145351861.1\|3241475_3242519_-\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|366542
NZ_CP036262.1\|WP_145351865.1\|3251108_3251591_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351858.1\|3238213_3238972_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351853.1\|3232488_3233994_-\|TolC-family-protein	unknown	unknown	gnl\|CDD\|224455
NZ_CP036262.1\|WP_145351860.1\|3240294_3241425_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145351855.1\|3235971_3236238_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145351866.1\|3251624_3252683_+\|low-specificity-L-threonine-aldolase	unknown	unknown	gnl\|CDD\|178323
NZ_CP036262.1\|WP_145351851.1\|3229911_3231375_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293751
NZ_CP036262.1\|WP_145351857.1\|3237020_3237992_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187541
NZ_CP036262.1\|WP_145355257.1\|3244360_3247312_+\|DUF5117-domain-containing-protein	unknown	unknown	gnl\|CDD\|379818
NZ_CP036262.1\|WP_145351867.1\|3252673_3254326_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227621
NZ_CP036262.1\|WP_145351856.1\|3236496_3237030_+\|gamma-carbonic-anhydrase-family-protein	unknown	unknown	gnl\|CDD\|223735
NZ_CP036262.1\|WP_145351854.1\|3234820_3235975_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340839
NZ_CP036262.1\|WP_145351852.1\|3231454_3232372_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225256
NZ_CP036262.1\|WP_145351863.1\|3248088_3249558_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227665
NZ_CP036262.1\|WP_145351864.1\|3249884_3250832_+\|DUF1571-domain-containing-protein	unknown	unknown	gnl\|CDD\|377879
NZ_CP036262.1\|WP_145351850.1\|3229020_3229854_+\|DUF1853-family-protein	unknown	unknown	gnl\|CDD\|378094
NZ_CP036262.1\|WP_145351859.1\|3239808_3240195_-\|glyoxalase	unknown	unknown	gnl\|CDD\|319909
NZ_CP036262.1\|WP_145351862.1\|3242699_3243950_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380413
NZ_CP036262.1\|WP_145351849.1\|3227523_3229017_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293750

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145351861.1\|3241475_3242519_-\|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.	2.12449e-08
NZ_CP036262.1\|WP_145351853.1\|3232488_3233994_-\|TolC-family-protein	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	6.8971e-22
NZ_CP036262.1\|WP_145351860.1\|3240294_3241425_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.29875e-76
NZ_CP036262.1\|WP_145351866.1\|3251624_3252683_+\|low-specificity-L-threonine-aldolase	gnl\|CDD\|178323	PLN02721, PLN02721, threonine aldolase.	5.19003e-121
NZ_CP036262.1\|WP_145351851.1\|3229911_3231375_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293751	cd16027, SGSH, N-sulfoglucosamine sulfohydrolase (SGSH; sulfamidase). N-sulfoglucosamine sulfohydrolase (SGSH) belongs to the sulfatase family and catalyses the cleavage of N-linked sulfate groups from the GAGs heparin sulfate and heparin. The active site is characterized by the amino-acid sequence motif C(X)PSR that is highly conserved among most sulfatases. The cysteine residue is post-translationally converted to a formylglycine (FGly) residue, which is crucial for the catalytic process. Loss of function of SGSH results a disease called mucopolysaccharidosis type IIIA (Sanfilippo A syndrome), a fatal childhood-onset neurodegenerative disease with mild facial, visceral and skeletal abnormalities.	1.17572e-133
NZ_CP036262.1\|WP_145351857.1\|3237020_3237992_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187541	cd05230, UGD_SDR_e, UDP-glucuronate decarboxylase (UGD) and related proteins, extended (e) SDRs. UGD catalyzes the formation of UDP-xylose from UDP-glucuronate; it is an extended-SDR, and has the characteristic glycine-rich NAD-binding pattern, TGXXGXXG, and active site tetrad. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	0
NZ_CP036262.1\|WP_145355257.1\|3244360_3247312_+\|DUF5117-domain-containing-protein	gnl\|CDD\|379818	pfam16313, DUF4953, Met-zincin. This is a family of uncharacterized proteins that carry the highly characteristic met-zincin mmotif HExxHxxGxxH, the extended zinc-binding domain of metallopeptidases.	1.14564e-73
NZ_CP036262.1\|WP_145351867.1\|3252673_3254326_+\|hypothetical-protein	gnl\|CDD\|227621	COG5305, COG5305, Predicted membrane protein [Function unknown].	7.81779e-06
NZ_CP036262.1\|WP_145351856.1\|3236496_3237030_+\|gamma-carbonic-anhydrase-family-protein	gnl\|CDD\|223735	COG0663, PaaY, Carbonic anhydrases/acetyltransferases, isoleucine patch superfamily [General function prediction only].	1.41627e-83
NZ_CP036262.1\|WP_145351854.1\|3234820_3235975_+\|glycosyltransferase	gnl\|CDD\|340839	cd03811, GT4_GT28_WabH-like, family 4 and family 28 glycosyltransferases similar to Klebsiella WabH. This family is most closely related to the GT1 family of glycosyltransferases. WabH in Klebsiella pneumoniae has been shown to transfer a GlcNAc residue from UDP-GlcNAc onto the acceptor GalUA residue in the cellular outer core.	2.07436e-76
NZ_CP036262.1\|WP_145351852.1\|3231454_3232372_-\|hypothetical-protein	gnl\|CDD\|225256	COG2382, Fes, Enterochelin esterase and related enzymes [Inorganic ion transport and metabolism].	0.00169726
NZ_CP036262.1\|WP_145351863.1\|3248088_3249558_-\|hypothetical-protein	gnl\|CDD\|227665	COG5373, COG5373, Predicted membrane protein [Function unknown].	3.09636e-05
NZ_CP036262.1\|WP_145351864.1\|3249884_3250832_+\|DUF1571-domain-containing-protein	gnl\|CDD\|377879	pfam07608, DUF1571, Protein of unknown function (DUF1571). A family of paralogous proteins in Rhodopirellula baltica.	6.43765e-80
NZ_CP036262.1\|WP_145351850.1\|3229020_3229854_+\|DUF1853-family-protein	gnl\|CDD\|378094	pfam08907, DUF1853, Domain of unknown function (DUF1853). This family of proteins are functionally uncharacterized.	2.56891e-62
NZ_CP036262.1\|WP_145351859.1\|3239808_3240195_-\|glyoxalase	gnl\|CDD\|319909	cd07245, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	1.09631e-25
NZ_CP036262.1\|WP_145351862.1\|3242699_3243950_-\|hypothetical-protein	gnl\|CDD\|380413	cd07010, cupin_PMI_type_I_N_bac, Phosphomannose isomerase in bacteria and archaea, N-terminal cupin domain. This subfamily contains type I phosphomannose isomerase (PMI; E.C. 5.3.1.8; also known as mannose-6-phosphate isomerase) found in many bacteria (e.g. Bacillus subtilis) and archaea. PMI catalyzes the reversible isomerization of fructose-6-phosphate (F6P) and mannose-6-phosphate (M6P), the first committed step in the synthesis of mannosylated glycoproteins. The active site, located within the N-terminal jelly roll-like beta-barrel cupin fold, contains a single essential zinc atom and forms a deep, open cavity large enough to contain M6P or F6P. PMI type I also has a C-terminal beta-barrel fold which has diverged considerably from the N-terminal domain and is not included here. This subfamily does not contain an alpha helical domain that exists in eukaryotic and some prokaryotic PMIs. F6P is a substrate for glycolysis and gluconeogenesis, while M6P is a substrate for production of activated mannose donor guanosine 5'-diphosphate D-mannose, an important precursor of mannosylated biomolecules such as glycoproteins, bacterial exopolysaccharides and fungal cell wall components. PMI is also essential for survival, virulence and possibly pathogenicity of some bacteria and protozoan parasites, as well as for cell wall integrity of certain yeasts. Thus, PMI is a potential target against fungal infections causing serious illness or death.	1.18781e-09
NZ_CP036262.1\|WP_145351849.1\|3227523_3229017_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293750	cd16026, GALNS_like, galactosamine-6-sulfatase; also known as N-acetylgalactosamine-6-sulfatase (GALNS). Lysosomal galactosamine-6-sulfatase removes sulfate groups from a terminal N-acetylgalactosamine-6-sulfate (or galactose-6-sulfate) in mucopolysaccharides such as keratan sulfate and chondroitin-6-sulfate. Defects in GALNS lead to accumulation of substrates, resulting in the development of the lysosomal storage disease mucopolysaccharidosis IV A.	0

>NZ_CP036262.1|WP_145351858.1|3238213_3238972_+|hypothetical-protein
MKNRTLPILAGLLFLSSAWTAPAFAQSALPQGPSFRLETEIYDADGNTPLARHKILFDSGVIYDLEEMGGTIQTIFDPTRERVVLLDTKAQLQAELSTQQLIDATVQLSAAARQNSKAAAFGLDAEVVQTGDQYAVKFGSCKYETTTQELSRPEFAHAYHELTVWAARLNVLRRVGVPPFGRMALGEKLSAAGLVPLELTLSIDEGSKVQRYRAHHLVIETLSELDRRAIQKVGDNLANFRKVSLEEFPSES
>NZ_CP036262.1|WP_145351857.1|3237020_3237992_-|NAD-dependent-epimerase/dehydratase-family-protein
MIHRILVTGGAGFLGSHLCERLVEEGHDVICLDNFFTSQKSNVVHLLNRPNFELIRHDITLPIFLEVDQIYNLACPAAPGHYQFNPIKTMKTSVMGVINMLGIAKRCGARFLQASTSEVYGDPDVHPQPESYRGSVNPIGPRACYDEGKRAAESICMDYRRSNNVDARIVRIFNTYGPRMHPYDGRVVSNFIRQALRNEPITIFGDGEQTRSFCYRDDLVEAIVRMMNNSEGFAGPVNIGNQGEFTIRQLAEMVMEKVGGESKLVQKPLPTDDPTRRRPDIRLAKEKLDWEPTTPLSEGLQKTIDWFRSIDIDDYQPPTPNYS
>NZ_CP036262.1|WP_145351856.1|3236496_3237030_+|gamma-carbonic-anhydrase-family-protein
MTIYQLGEKCPKIDPSAYIAAEATIIGDVEIAADANVWPGAVARGDVEPIRIGARSSVQDNVVMHTDPGFPLHIGEDATIGHQATLHGCTIGRGALVGMQAVVLNGAEIGEGSLVAAGALVTEGKSFPAHSLILGSPAKVARPLREDEIKNIQALAARYVERGRDYRENLKPVTPQE
>NZ_CP036262.1|WP_145351855.1|3235971_3236238_-|hypothetical-protein
MARAAKTLNPNAPLTTREENVLRVFREFLMRPGQMLCFHGPDLDRHRESLETLTDRDLLVSESFKGGYSLTTEGFEAMKACTSRPAPR
>NZ_CP036262.1|WP_145351854.1|3234820_3235975_+|glycosyltransferase
MSERISVLLMIGSLAGGGSERQMIGIAKMLDRTKFRPVLFLIYASGELLKEVPADVPVYAYWQDQKPFRFNYPGRILRDQKRYLEKVLRKESIDVLYSRTYPMALVAGPVTKRLGVPHLPTIVVDPASMLRDSKERWMRLKLLLLKRAYHDSELVLTVSEGVREAAIAFYDLPPPHVRRMINSLDLERLDRLAEQPFDHFRPGRFHIVHAGRFVSQKGHRYLFEAIAELVRRGHRELSVHLYGEGPDQDSLQQLVAKLGLQDHVELNPYLVNVLPAIKNADLFCLPSLYEGMPNALLEAVALGIPVVSTDCPSGPREILNEGELGRLVPVADSVAMADAIAEVIENKQAAFEWAARAKKEIRARFDPAAVTPVLEQILESAVGS
>NZ_CP036262.1|WP_145351853.1|3232488_3233994_-|TolC-family-protein
MRPIAERFQFDRTESAVETTADIPPQFAPPAPQKDLAATAIQQTAHDASEPSAGDSETANAVAQASGFEASNLTALVPFTIADPPFPADSEPAAQPTSGMTLEAFESLALTNNPTIGALVATTRKAAGFRTQVGLRANPTIGYSGSQLDDEGTDQHSVFISQTIITADKLELNRRVLDRALRTQLLHLEAQKYRVATDVRVKFYDALAAQERMRLVQDFQKVANKGLELSELRKEALEGSQLDIVQAKVQKNEIDLVLQQAEIAYSAAWRELAALAGSPHLSPTPLIGTLPQTDVAMDWTELTATTVYSSPEYQAAQAKVSQARANIDRQEIQAIPNFDFNLAGGHDNGTDSGFINVQVGAPIPVFNRNQGNLSAARGELMRACREVQRIENSIQARIAIVSQQYDSALAAVAMYNNEILPNAAEGLKLAETAYRAGETSFVQVLVARRTYYDTNLQYLKSQTRLAQARTRLDGYVLSGALDAIVDESGDDSLRGQTFSQQ
>NZ_CP036262.1|WP_145351852.1|3231454_3232372_-|hypothetical-protein
MHKRLLVLTIAVYAALGIQASDHQPLDVDSQQVLEIPGISSGDPAAGKRVVVKAPEFASTSVFHTIYLPPGWTPTGKQYPIIFEYTGNRFPQSGSTGQTEDAALGYGLTAGKCIWVSLPYVSADHQKNEVTWWGDELATVEYAKLNVPRIIQTYNADPNAVILCGFSRGAIGVSYIGLHDAEIAKLWTIMVTHDHFDGVRSWGGTEWGQPLSEYQHRAASRLKRIGNRPLLVIQNGDIRATRSFVKQTIGAPDNVSFMQINANEILGAFPNSIAKSAHTDRWLLPPSSARSEVWAWINRSLAAAE
>NZ_CP036262.1|WP_145351851.1|3229911_3231375_+|sulfatase-like-hydrolase/transferase
MGETMSRIFALLLGTCWLAGSVLADQTQPAQPSKPNVLWIYVDDMSDWMGCYGDSLALTPNIDSLAEGGVLFERAYMPAPVCSTTRSALITGTMQTSYGLHQHRTMIKEELAEGLLTVPELFRRAGYLTFNEAKDDYNFKRERSLMYSPEFERPKINSHLVGRDLSWLKQLQGKSFFGQIQLKGGKFGGETGAKFPADSLVADDAVSVPPQYPDHPVFRNAIARHYAQIAETDAQVGAIITALKEYGLWENTYVFFFTDHGSPLPRAKQFLYEEGTKVPLIVHGTESDSLVSGGASRRSDLVSGIDITMTSLALADIAIPDFMEGKDLFADDYQPRTYLISARDRMGNAIDRIRSVSSQHFRYIRNYKTDRALFQPQYRDGYATFETFQKMRRRNLLSPVQASYFDSENRPAEEFYDLRDDPHQVVNLAEDPKYETAIADHRRFLHEWEEATDDKGRYPESKESLKEVFEHAAGKCVAPEFDFLRTQ
>NZ_CP036262.1|WP_145351850.1|3229020_3229854_+|DUF1853-family-protein
MLQSQELRDLTWVVESPFLLNPHPDLPKFDWRSVSLSQLTAFCQEKPSRRVGRYFEGLVLYWLQHVRKIQVVAESLQVRSGKRTLGEIDFLFRDESSKLTHWEVAVKFYLFHPNRTFAGSHYIGPNAGDTFERKRERMFRHQLPLSETHFPDVQQRNAFVKGRIFYHPDDGSQPQLPEGLAPDHLRGNWIHAFELVGWIRKQDGRHAILNKPYWLSPAEFDQDGDCGLSDHETIERLTRHFQEAAHPVLVSHLCESDGLWQETSRTFVVPDHWPGTG
>NZ_CP036262.1|WP_145351849.1|3227523_3229017_+|sulfatase-like-hydrolase/transferase
MSRRAFSSSPLPANDLLPEGSIVLRRPSKVLFALALCFSGFAQTFFGAELLADSQSSPNFIVIFTDDQGYNDLGCFGSKTIKTPHIDRLAAEGRKYTSFYTACSVCSPSRAALLTGSYPKRVGMHKHVLFPKSDYGLNPSEYTIADHLKSQGYATACVGKWHLGHHPEILPRANGFDSYYGIPYSNDMNHPDNARKSKIASDRLWESQGTSITYWNTPLFENEEIVELPVDQRTITRRYTDKAIDFVTENQDKPFFLYLPHSMPHIPLYVPEDVYDPDPQNAYKCVIEHIDAEVGRLADTVRELGLDKNTYIIYTSDNGPWLQFKNHGGSADPLRAGKGTTFEGGQRVPCVVWGPGRIPAGTQCDAMTSTMDLLPTIASLSGAPLPDIPTIDGYDITGTFKTNESPRNELLFYSSVGALQGIRLGDWKYLEVVSRPNARKSKTGKPSVGIYLFQLSDDIGEQNNLIDQHPEIAAKLKARMQEADAEITANARPVWRK
>NZ_CP036262.1|WP_145351859.1|3239808_3240195_-|glyoxalase
MRTINLNHVALHVTDVERSIAFYRDALGLEVLPRPAFDFPGAWFRVGTDQELHLIGDRELDVHSGHRGTHIAIQVEDLDAWDAHLSKELEKHGASRVPRKTRPDGAQQSFLIDPDGHWVELCELPKAK
>NZ_CP036262.1|WP_145351860.1|3240294_3241425_-|Gfo/Idh/MocA-family-oxidoreductase
MKPLNIGMIGYGFMGKAHTNAYKQANNFFDCEYKPVLKALCARNRDKAEGFAKNWGYESIETDWRALLKRDDIDAVDICTPNNLHKEIAIEAAKAGKMILCEKPLAMNTAEGEEMCEAVEAAGVPNMVWYNYRRVPAVSLAKQLIDEGRLGKIFHYRANFLQDWTINADVPVGGAATWRLDAEAAGSGVTGDLLAHCIDTALWLNGGIKDVTAMTETFVKERTHADTGEKIPVTIDDACSFLCHFNNGSLGLFESTRYARGHKALYTLEINGEKASLRWDLHDLHRLEYFDHADDSIVRGWRSIHVSDGDQPYMGNWWVPGLQIGYEHSFIHQVADFLKSLESDAPFSPNFRDALETQKVCDAVLASAKQRVWKDV
>NZ_CP036262.1|WP_145351861.1|3241475_3242519_-|TIM-barrel-protein
MNNFPKLHNAAWPGVVGKGGEGDDPIIELDQLLDMTASAEVNGRRFDGVDLFLFDPHVSIDATDAELEDLAERVRSRNLDIGTVVAPVWEPTGGGPAMGGPEEVEAFLTQVRKACQIGQKLRQIGVRPHGVIRLDSASSVSEWVKDPEGNQSKIADTFKAACDIAEEYDERLAAEGEICWGGMQSWRKMVDLLERVGHPERLGFQADMAHTLLYLMGYNAPEDAIVASDFDWSDTAAKEAALKELTHALRPWTIDFHVAQNDASVHGTGSHDKTGRHCLPDDPNGKLDIAKDAGFWLRDEHGDVLKTIKHICWDGCMFPNEVMTKPDTWNKILASMLEVQAAHGWQE
>NZ_CP036262.1|WP_145351862.1|3242699_3243950_-|hypothetical-protein
MNIALDEGLVKGDSVASLLDSALDAGGGLLRLTPTWVPRSFLHPGRRIKLHPGDYYRFGADRGGIDERWFGSTTEAANEGRVWHEGLSFCLFEGKKFLLKDAVEEAGARLIGSAIADKYNRWPVYSKFFDNMGPIPHHMHQSFEDAKLVGQEGKPESYYFPPQLNNVDNNFAYTFMGLEPGTTKEDVRKCLENWNAGDNGILDLSRAYRLKRGTGWLIPPGVLHAPGSLCTYEPQWGSDVFGMYQSIVEGRYVPWSLLVKDMPEEKHQDLDFIVGQLDWERNVDTHFKNSNYLEPIRDEANSGDKFEDLWIVYGTVDKQQLFSAKELTIQPGAKCVLNDPGASSWITVQGKGKMGALNLQTPAMIHFGENTEDEVFISHEAATNGVQIENTGSEPLVGLRYFGPDVHGNNIPKAGS
>NZ_CP036262.1|WP_145355257.1|3244360_3247312_+|DUF5117-domain-containing-protein
MHCLIPTSLFAATGRAILTLATLAVPVVAVAADSLPEFSKVSEGYEEIAPSDQQDVKGLFKVWKREKDGQVIGELPKNFATKKYFLALTVSSGDKYAGLQSGDWVVQWRKYNDRLALIAPNLTIRATGDDEAKASVKRLFTDQVLLDVPILATGPSGGPVVDLDSLLVGNATKFFGNSVRVTNPRLVALKQAKVFKKNIELAFEIVGASSKLQTIHYSISEVPATNNGYTPRAADERIGYFTTSFTDLGKYDDDETRIRYINRWHLEKRDPKLKLSPPKEPIRFYIEHTTPVRYRRWIKEGIEFWNKAFEEVGFVDAIVVEYQDAATGIHMEKDPEDVSYNFVRWLNNDVGTAIGPSRVHPETGQILDADIILTDGWIRHFRFNYHDLMPQLAMEGMGPDTLAWLAEHPSWDPRVRFASPSKALHLRQQAAMAGSLPASGHPFAAADPMLLGDDEYDGLYGRVSQKNGLCMAASSRGMEMALARMNWALTLLDDKANDDKKKDDGEEKKEKTDEEKKEEVTKSDKDKDEAKEDESLLDGMPEWFVGPLLADLVAHEVGHTLGLRHNFKASAMLTLDEINSRDVKGKKTITASVMDYTPINYRYESGEIQGDYGMIDLGPYDFWAIEYGYVLDAKKLPGILERCTEPALQFATDEDTSGPDPLARRYDFGRDPLAFANEQTKLVQLYRERILDEFVEDGDGWGKARRAYELTLGLQVRMINMMANWVGGTSIHRDRKGDPGDRDPVEVIPAEQQREALKFVIDQAFNDQAFGLNPELLARMSVDKWLDSSSRSQIATEGAWPIHDRVLGVQSSALTLLMNPTTLRGVYDNELRVAADVDVLTLPELLNTISEATWAELSAECPEDRDDRRPMISSLRRNLQREHVERLLDLVLATKSQGAASKPISNLARLHLKELQGNIQKSLESCGDKMDVYSKAHLSELDERIGSALKAGYTYGSANAGGGIMQIRFGQPTDQSRDQVFPQ
>NZ_CP036262.1|WP_145351863.1|3248088_3249558_-|hypothetical-protein
MRFLKHPLREARMHSSGPTAYLTCGLLIVFSCGCQSPLADRSVRVTENSPEALQAAEQPRTLLAERQKPAVPESTAVSSSLSDTHASIDGGTLADSEALLQAFQNAGPEVQEAARRRMLASQQSNVKVNPLPDLPTQSDLDLDPFDRPLELPNETTTIANITDAMKEDSKSQQAAPNADAFRTAISDEIAASGFVVPTSHSSESATTETVADLAEPPAAPAGVPEPQPESPIEPAPTEPTAELATPTPAAPKAPVSEAALMASLLEQMSAAPTDDNDTNKMRQAMRYRLQLVLAGRIDEAVEPIEGLDSSEQEFFRNQVLALWTAIDPQGHPVPQRRWTTALPQLREAVSHLAAATGTLEVRNLAFCTDVESYGRIKTFDSMRFNPGQQVILYSEVDSFAAERLSTGYETQLQGSYEIFDSSGKRIAEKVLPTDQQVCNNYRRDYFIAYRLHLPSQLADGKYRMELTMEDLKGKKYGQSSIEFEISNAR
>NZ_CP036262.1|WP_145351864.1|3249884_3250832_+|DUF1571-domain-containing-protein
MAFRQDQWRRQFVTAFMLIGLCSSLGYAQPLPGQQPVFRQAYESAPEQERNAADASPVAANQIALAANTKIPESTGAHPLEPALKMARESLQHIQGNVDDYTALFVKRCRVDGVLPEMQYSNVKIRNRKVEAGKIKVPLSVYIDFLRPAKVRGREVIWVENKNDGNMVVHESGLKNFMNVNLAPDSYLAMRGQKHPISEIGIENLAVKLIETGERDLQYDECEVKFFNDAKVGKEVCTMLQVIHPVERAHFDFYCARVYFSNELNMPIRYESWSWPETADGKPVLEEEYNYVNVKVNVGLTDNDFDTDNAEYRFW
>NZ_CP036262.1|WP_145351865.1|3251108_3251591_-|hypothetical-protein
MMHQFGQQSPFVNHHPSPEAAMSPSSSSNPYQSPPSVIHKGVIYGDNALRRKGGFLYREIELSGPFTGILIYNGWWFLQRISLNGQRLWSQISWLTLQRTIDFQIPVCQEQGSPIASPNGTADSMITLHPARLQIDFDSRLKFRRFQLLIDEVSVYDEIV
>NZ_CP036262.1|WP_145351866.1|3251624_3252683_+|low-specificity-L-threonine-aldolase
MIDLRSDTVTRPTAEMRRAMADAVVGDDVIDIDPTVAALQSETASLLGKEAALFMPSGSMANQIAVRVHCTRGSEFLCEADCHIYQYEQAAFAQLSGLVAKTIQGDSGILLPSQLSDQIRPHNDHMVRTEMITLENTHNRGGGTIQPLQTVIEICEWAEKNGLRRHLDGARLWNAIEATGVDAKQWADPFDSVSVCFSKGLGAPVGSVLAGSKPFIAEARRTRKLFGGGMRQAGIIAAGALHALRHHRPRLAVDHQHAQRLAAAVEECPGLSLGAAGVQTNIIFAFIDPAWGTAKQLVDLLREEQVACMAMLPQAIRLVTHMDVDSDQIDRAAEALRKIMASGPGSDASGCK
>NZ_CP036262.1|WP_145351867.1|3252673_3254326_+|hypothetical-protein
MQVNEAPDFSRRRLTLLSLGLAVLTVALRWSFCHESLWVDELHSAWAVWDELALVSERSSAGNQTPWYFWGLWAWKQIFGGSEVALRAPSLLASAISVFAITWAAAVHSRQFVVGLLAGGLLAVEFRAVEFGTEVRVYALLIVLSILSARGWLTVLESSESSDAVETPWSLPWFRKVAMIWLPGFAAVLLHPTAALTVGMLAAVGGVLGITTQKRVRTAIYAAAGSIGFVLLALAVNGVAVRNVWSIRHQWAQFAIPRSGIELYRMWPWQLVIAAVLALIVVVVGCRVFCGNRAKTEGTKQPKSNAALLCLGTVLAATTLCWVVAFLEWLPMWHVRYLIGLLPLMMWGTADLWGIVFAKMNCTRMRFLTASMNGAIAVCLVGWLVHSQGTWWLWMPTKPNVPNVVLRGEDWRSAIAWLQDHRQANEPVYLGAELIESSLLTDGVEDASADRLKEYLLFPTSGPYAIDVKEPLGLAFLSMRSDLKRILAPSPQQGVKVRWLVYRMDEASVEQAYNQANLPDIASPAIARTNGATEAFGGVTIVRLETQAEE

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Crispr_ID: NZ_CP036262_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_13

4669840-4669978

Orphan

Consensus_repeat	Method
AAAGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAAACAGTTCCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_13

>merge|NZ_CP036262|13|4669840-4669978|CRISPRCasFinder
AAAGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAAACAGTTCCTAGCGGCAGGGCGCGAGTCCTCCGGCCCGTCGACACCAAACGCTTAAAAGGAAAAGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAAACAATTCCT

>NZ_CP036262|13|11|4669840-4669978|CRISPRCasFinder
AAAGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAAACAGTTCCT	AGCGGCAGGGCGCGAGTCCTCCGGCCCGTCGACACCAAACGCTTAAAAGGA
AAAGGCCGGACGGCTTGCGCCGTTCCGCTAAGAAAACAATTCCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145352783.1\|4684755_4686000_+\|NO-inducible-flavohemoprotein	unknown	unknown	gnl\|CDD\|237337
NZ_CP036262.1\|WP_145352776.1\|4665233_4666013_+\|DUF3386-family-protein	unknown	unknown	gnl\|CDD\|371771
NZ_CP036262.1\|WP_145352773.1\|4660849_4661134_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352785.1\|4687218_4687527_-\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|239604
NZ_CP036262.1\|WP_145352771.1\|4656149_4658354_+\|S46-family-peptidase	unknown	unknown	gnl\|CDD\|371067
NZ_CP036262.1\|WP_145352778.1\|4670034_4671108_-\|S-methyl-5-thioribose-1-phosphate-isomerase	unknown	unknown	gnl\|CDD\|235578
NZ_CP036262.1\|WP_145352784.1\|4686135_4686471_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380358
NZ_CP036262.1\|WP_145352782.1\|4683489_4684191_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352772.1\|4658671_4660516_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293765
NZ_CP036262.1\|WP_145352769.1\|4654025_4654613_+\|imidazoleglycerol-phosphate-dehydratase-HisB	unknown	unknown	gnl\|CDD\|153419
NZ_CP036262.1\|WP_145355475.1\|4686563_4687205_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274701
NZ_CP036262.1\|WP_145352781.1\|4673726_4683449_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369473
NZ_CP036262.1\|WP_145352774.1\|4661178_4662117_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145352786.1\|4687532_4687985_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352777.1\|4668521_4669748_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225153
NZ_CP036262.1\|WP_145352775.1\|4663852_4665139_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036262.1\|WP_145352779.1\|4671147_4672584_-\|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl\|CDD\|180579
NZ_CP036262.1\|WP_145355473.1\|4666249_4668295_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|378963
NZ_CP036262.1\|WP_145352770.1\|4654973_4656008_-\|DUF1593-domain-containing-protein	unknown	unknown	gnl\|CDD\|377887
NZ_CP036262.1\|WP_145352780.1\|4672708_4673317_-\|30S-ribosomal-protein-S4	unknown	unknown	gnl\|CDD\|235411

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145352776.1\|4665233_4666013_+\|DUF3386-family-protein	gnl\|CDD\|371771	pfam11866, DUF3386, Protein of unknown function (DUF3386). This family of proteins are functionally uncharacterized. This protein is found in bacteria and eukaryotes. Proteins in this family are about 220 amino acids in length.	1.33786e-33
NZ_CP036262.1\|WP_145352785.1\|4687218_4687527_-\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|239604	cd03528, Rieske_RO_ferredoxin, Rieske non-heme iron oxygenase (RO) family, Rieske ferredoxin component; composed of the Rieske ferredoxin component of some three-component RO systems including biphenyl dioxygenase (BPDO) and carbazole 1,9a-dioxygenase (CARDO). The RO family comprise a large class of aromatic ring-hydroxylating dioxygenases found predominantly in microorganisms. These enzymes enable microorganisms to tolerate and even exclusively utilize aromatic compounds for growth. ROs consist of two or three components: reductase, oxygenase, and ferredoxin (in some cases) components. The ferredoxin component contains either a plant-type or Rieske-type [2Fe-2S] cluster. The Rieske ferredoxin component in this family carries an electron from the RO reductase component to the terminal RO oxygenase component. BPDO degrades biphenyls and polychlorinated biphenyls. BPDO ferredoxin (BphF) has structural features consistent with a minimal and perhaps archetypical Rieske protein in that the insertions that give other Rieske proteins unique structural features are missing. CARDO catalyzes dihydroxylation at the C1 and C9a positions of carbazole. Rieske ferredoxins are found as subunits of membrane oxidase complexes, cis-dihydrodiol-forming aromatic dioxygenases, bacterial assimilatory nitrite reductases, and arsenite oxidase. Rieske ferredoxins are also found as soluble electron carriers in bacterial dioxygenase and monooxygenase complexes.	1.78716e-33
NZ_CP036262.1\|WP_145352771.1\|4656149_4658354_+\|S46-family-peptidase	gnl\|CDD\|371067	pfam10459, Peptidase_S46, Peptidase S46. Dipeptidyl-peptidase 7 (DPP-7) is the best characterized member of this family. It is a serine peptidase that is located on the cell surface and is predicted to have two N-terminal transmembrane domains.	0
NZ_CP036262.1\|WP_145352778.1\|4670034_4671108_-\|S-methyl-5-thioribose-1-phosphate-isomerase	gnl\|CDD\|235578	PRK05720, mtnA, methylthioribose-1-phosphate isomerase; Reviewed.	3.60499e-166
NZ_CP036262.1\|WP_145352784.1\|4686135_4686471_+\|cupin-domain-containing-protein	gnl\|CDD\|380358	cd02230, cupin_HP0902-like, Helicobacter pylori HP0902 and related proteins, cupin domain. This family includes prokaryotic and archaeal proteins homologous to HP0902, a functionally uncharacterized protein from Helicobacter pylori and Spy1581, a protein of unknown function from Streptococcus pyogenes. These proteins demonstrate all-beta cupin folds that cannot bind metal ions due to the absence of a metal-binding histidine that is conserved in many metallo-cupins. HP0902 is able to bind bacterial endotoxin lipopolysaccharides (LPS) through its surface-exposed loops, where metal-binding sites are usually found in other metallo-cupins, and thus may have a putative role in H. pylori pathogenicity.	2.08779e-24
NZ_CP036262.1\|WP_145352783.1\|4684755_4686000_+\|NO-inducible-flavohemoprotein	gnl\|CDD\|237337	PRK13289, PRK13289, NO-inducible flavohemoprotein.	0
NZ_CP036262.1\|WP_145352772.1\|4658671_4660516_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293765	cd16146, ARS_like, uncharacterized arylsulfatase. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036262.1\|WP_145352769.1\|4654025_4654613_+\|imidazoleglycerol-phosphate-dehydratase-HisB	gnl\|CDD\|153419	cd07914, IGPD, Imidazoleglycerol-phosphate dehydratase. Imidazoleglycerol-phosphate dehydratase (IGPD; EC 4.2.1.19) catalyzes the dehydration of imidazole glycerol phosphate to imidazole acetol phosphate, the sixth step of histidine biosynthesis in plants and microorganisms where the histidine is synthesized de novo. There is an internal repeat in the protein domain that is related by pseudo-dyad symmetry, perhaps as a result of an ancient gene duplication. The apo-form of IGPD exists as a catalytically inactive trimer which, in the presence of specific divalent metal cations such as manganese (Mn2+), cobalt (Co2+), cadmium (Cd2+), nickel (Ni2+), iron (Fe2+) and zinc (Zn2+), assembles to form a biologically active high molecular weight metalloenzyme; a 24-mer with 4-3-2 symmetry. Each 24-mer has 24 active sites, and contains around 1.5 metal ions per monomer, each monomer contributing residues to three separate active sites. IGPD enzymes are monofunctional in fungi, plants, archaea and some eubacteria while they are encoded as bifunctional enzymes in other eubacteria, such that the enzyme is fused to histidinol-phosphate phosphatase, the penultimate enzyme of the histidine biosynthesis pathway. The histidine biosynthesis pathway is a potential target for development of herbicides, and IGPD is a target for the triazole phosphonate herbicides.	3.09246e-117
NZ_CP036262.1\|WP_145355475.1\|4686563_4687205_+\|hypothetical-protein	gnl\|CDD\|274701	TIGR03652, FeS_repair_RIC, iron-sulfur cluster repair di-iron protein. Members of this protein family, designated variously as YftE, NorA, DrnN, and NipC, are di-iron proteins involved in the repair of iron-sulfur clusters. Previously assigned names reflect pleiotropic effects of damage from NO or other oxidative stress when this protein is mutated. The suggested name now is RIC, for Repair of Iron Centers. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	1.70762e-48
NZ_CP036262.1\|WP_145352781.1\|4673726_4683449_+\|hypothetical-protein	gnl\|CDD\|369473	pfam07705, CARDB, CARDB. Cell adhesion related domain found in bacteria.	0.000412937
NZ_CP036262.1\|WP_145352774.1\|4661178_4662117_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	1.03285e-49
NZ_CP036262.1\|WP_145352777.1\|4668521_4669748_+\|hypothetical-protein	gnl\|CDD\|225153	COG2244, RfbX, Membrane protein involved in the export of O-antigen and teichoic acid [General function prediction only].	8.30204e-10
NZ_CP036262.1\|WP_145352775.1\|4663852_4665139_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	7.45374e-14
NZ_CP036262.1\|WP_145352779.1\|4671147_4672584_-\|dihydrolipoyl-dehydrogenase	gnl\|CDD\|180579	PRK06467, PRK06467, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP036262.1\|WP_145355473.1\|4666249_4668295_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	8.17694e-129
NZ_CP036262.1\|WP_145352770.1\|4654973_4656008_-\|DUF1593-domain-containing-protein	gnl\|CDD\|377887	pfam07632, DUF1593, Protein of unknown function (DUF1593). A family of proteins in Rhodopirellula baltica that are predicted to be secreted. Also, a member has been identified in Caulobacter crescentus. These proteins mat be related to pfam01156.	9.29972e-104
NZ_CP036262.1\|WP_145352780.1\|4672708_4673317_-\|30S-ribosomal-protein-S4	gnl\|CDD\|235411	PRK05327, rpsD, 30S ribosomal protein S4; Validated.	3.67742e-89

>NZ_CP036262.1|WP_145352777.1|4668521_4669748_+|hypothetical-protein
MCANIVGILLAYAATILLARNLEPSEFESYIGAIATLGLLASLGEGGIGKYSLKIVPQYVLQKEAGLLGGFLRFALGSAILLGILLAGLAAIIELAVQVEEREKVVLEALVYLPVMAVVGVAIDFLLAFRMPVFATLLARIVIPLTTLICIGLTIQAERLSPSTAVFAFGAGSLICLPIAIGANFTKSEPLTLDSRPIFLAGPWFLNSLSFLVFSFLTAWIFRAPLVIMHHIPHSGNELALLAPALETGCLVLLLAKSTDKYFQPMISEYLTTNNWAEGRKMRWLRLQWIGFGITGFLGLVFFFGRTILGWYGDKYVVAYPSLCVIAIGSSIWTICSLAPTYLQYTDALRRLLGSLLGHAILLTVLTVWLNRMFGTFGVALAYAVSISSLSLCNMWLASGRLREVRQA
>NZ_CP036262.1|WP_145355473.1|4666249_4668295_-|FAD-dependent-oxidoreductase
MGLFVGAFYCSSFVDAQSQATAPSVVVYGATPAGFCAAIAAAREGAAVTLVEPSHHVGGVNTGGLSFSDSNQTVRTTVMGLFDEWHTRIAADYAGRGQPLHYDVSEKNNAKWTYEPHVAARVTKAMLAEAGVDVQPNQVLTSVDLEAGRIQAILCKDRRFAADVFVDATYEGDLMAAAGVEWTIGREGRAAYSEKLAGKQYTKGTIPVSGLDSNGQLLPLLTATEGGDEEAGDRHVMVYSFRLCLTKNPENRVDFPAPETYDPKRFEAVRRYYLQVKRPHLLWDIYPLPNDKFDANNGIGKQFSMGLVGGGDDWCETPFTERSELWQKHRQYTLELYHFLTTDESVPEHLRKQMAEYGLCRDEFPETDHWSPQLYVREGRRMRGMHVLTENDVLRDPEKSDPIAVSSFPIDSHDCQRIGTAESIRNEGTIFPVRMAGRPHGYPYHVPYRSILPVKSDCENLLVPVALSATHVAFSSIRVEPTWMILGQSAGIAAALSAKQNVAVQDLPYPALQKQLLAQGQVLELPELAPLPPPAQPVGLKVSDLEGIVLDDATAEITGAWSTSRLFNPHIGSGYLHDGGDGEGDLSATFSGKVPASGNYEIRMAYSPHSSRSSRVPLEVRNGDTVKEFKVDQTVPLPVGQAFRKIGEIELRKGEPLTVTIRNQDCDGFVILDAIQFLPKL
>NZ_CP036262.1|WP_145352776.1|4665233_4666013_+|DUF3386-family-protein
MKRKELLRGIAAVLLLLPAIGHAEKPLDAPQKKGSSDQLARAAMKEAHDARAVWHHFPGFTAEVTIQTDAESHTGTILVTDDFDYELTISDDAIEPWIHSKLRSVIGHRRPGSAAVEVQVSEQKTSPEFGIFVARKDGSGTFRIENGLIREVLRKTDSNWLEITNVEMFDAGDGKVLPETSSVSYRDLQTGNLTKNVTNRFTWTRVGDFFLPSECFTIETGTEGSRQTRQLTFSNHKLTEPKKPLKVLESTSKLHNPLP
>NZ_CP036262.1|WP_145352775.1|4663852_4665139_+|PQQ-binding-like-beta-propeller-repeat-protein
MIASTCTLLAAICSAENPPWSKFQNGGRSTSDLTLPVEWAPDKNIAWTADIEGYGQSTPIVSHDQIVVTSTSGENKDNYHVSSFSIEDGSKNWQIDLTNPSPFANTPMVSRAAPSAIATANGFIAFFEGGVLAAISPEGKKQWEKNLVDTYGAIESRHGLSASLEQTNDLVFVWVERGEDPYILALDPTSGEEIWKAAGVGKTSWASPRLIPVDGGQHLVCSASGKIIGLDPSTGKRLWEFENISNNSSCTPTPAGEGQFLIGASDGRGESSAGSAAASNGLIQISKNDAGEYEANFKWHAKKATSTFGSPVVAGTTAAIVNRTGVLYRLDLETGEQVSVERTDAGGIWSTPIVAGGNIYLFGHKGTTSVISLADGKEIANNRCWAEAAAADDSSRSRGGNVLYAAAPAGNFLLLRRGDKLFAIGKTP
>NZ_CP036262.1|WP_145352774.1|4661178_4662117_-|DUF1559-domain-containing-protein
MSHKDFRARAGFTLVELLVVIAIIGVLVGLLLPAVQAAREAARRMSCSNQLKQIALATHNFHDTLLTFPYATRDRLEGDDGSTWATGHIQILPFLEGDAVASRWDPNEPRNSTVDSDGDGWTNDTLKKESIPTYLCPSMVPPSGPLTGERAPMSYLFSSGTPDASMLHYAVYYGLPEPAYDGAIIPVKTYLASGETAGPNHRKPTKFRDVIDGTSNTFLMGETDFMPKGVPSTSYGGVWAYGYAGYAWGTTYVPFNRHDNTSTVYGAFRSQHPSGGQFSLVDGSVRFVSETIDHAVYQAVSTRANGEVATLP
>NZ_CP036262.1|WP_145352773.1|4660849_4661134_-|hypothetical-protein
MKNKSFLTLIANTLLVILLGCGSDAGPAVSSGPLPPLSVEEWKQLPIQEKYDEATFERLRAKDEKLQAERAWGRFMREVVVPERKRDIPGIPGQ
>NZ_CP036262.1|WP_145352772.1|4658671_4660516_+|sulfatase-like-hydrolase/transferase
MSQYFAKTSSADQKRVGGQPGPASSTLPLTALAVPFLAALSALFLSPIARQATAAERPNIVMILADDQGWGDLSLHGNTNLSTPNIDSLAADGVAFENFYVSAVCAPTRAEMLTGRYFIRTGVRGVTRGDERLNLDEITIADTFQKAGYRTGAFGKWHNGSQPPYHPNDRGFDEYYGFTSGHWGTYFEPPLDHNNTAVKGKGYLVDDLTNHAIEFIEENKSEPFFCYVPLNTPHSPMHIPDRFYEKFDGVDLKMRNRDPEKEDELFSRAALAMVENIDWNVGRILQVLDEQNLAENTIVIYFSDNGPNSWRWNGDMKGRKGSIDEGGIRVPCLIRWPRKLAAGKKIDQVAAAIDFLPTLSDLANVELISEKPLDGRSLEPLLLGDGKDWQDRALLSFRKGASLRTQRFRIDGAGKLFDIENDRSQRHPVNEKFPKVSERMQDLLAKQTAEMKQIIATAPARPFTVGYGKRTVLPARDGEAKGGVERSARAPNNSFFTNWIDPKGAIEWNIEVGESGPYHVVVHHTCPTENVGTSIRVAIGDATAVAKVDKAFDPPLEGAAQDRASRGSESYVKDFAPLDFGMMDLEKGVHTLRLSTEALVGGRSIDVHSVELTK
>NZ_CP036262.1|WP_145352771.1|4656149_4658354_+|S46-family-peptidase
MPCQACPTSPHVFPLSCSRLFGFITLLCGVGCSLTAIAEEGMYPMSELRSLDLAARGIELTADQIFKPHANSLVDGVCKVNGCTGSFVSPKGLIITNHHCAYGAIQQASQGKQDYLTDGFQANTQQDEIPAPDYVVRVTEDYRDVSQEVLSAVRQDMTFLERTKAIEKKSKEIEFAAEQAAPQFRAEVAEMFAGESYVLFRYTYLKDIRLVFAPPQSVGNFGGEIDNWMWPRHTGDFSFMRAYVAPDGSSATYHADNVPYEPQRFIQVSAAGVEEEDAVFLLGYPGRTARHKTSAFLLYEQNLRLPTIIDLYNSQMAIMENAGKDNREVEIKHASRMRSLSNVEKRSRGQLQGLVRADIVKNRQDQEAELQKFIESEPANREQFGTLQAEIEAVYDQMTAAAPLEINLNQLRSASRAASFAFFVIDAAHERQKPNLDRETPYLDKNWDQSLQKLKSSVNDYHQATDQAILADILQRLALVDAEQTIPALTPLLASAEAIPTVSAQLVEQTKLDDWNFLEECLAMDVQQLNEVKDPLLQLMLQLYPTYLQIRETQKTREGELSELYGRLLLIKRRFMQTNFVPDANATLRFTCGHVRRYSPEDAVIKTPLTTLSGVIAKTTGVAPFITPAEVIAKQQAGDLGPFRSPELDDVPVAILYDTDTTGGNSGSPILNGRGELVGVNFDRCFEATINDFAWDQSYSRSIGVDIRYVLWLTGIVYGADHLLDEMGIDMPAN
>NZ_CP036262.1|WP_145352770.1|4654973_4656008_-|DUF1593-domain-containing-protein
MLNRCCRLLVLGVVLGTLFAMHSQANADERPRLLVLTDIGGDPDDRQSMIRLMVYSNAFRIEGLVATASGVPGELKEKITQPHLIREIVSAYGEVRPNLAKHEEGWPTVEQLSGVIKTGSPQRGRKHIGKGNDTEGSAWLIERIDAGSPEDPLNIAIWGGQSDLAQALWRVQTDRSAAEYAKFVKRFRVYDIADQDRIANWMHEQFPGLYYILSRAPAGKDSRTATFRGMYLTGNEQLTSEEWIRENILGTGPLGSRYPLKTHTNPNPYGCLKEGDTPSWFFFLPKGGNDPTDPTKSGWGGQFYQASDGWYRDDGPHYREARETVSRWREKFQEDFALRMSWSK
>NZ_CP036262.1|WP_145352769.1|4654025_4654613_+|imidazoleglycerol-phosphate-dehydratase-HisB
MSRKTTIDRQTGETQIRLSIDLDGSGAGERKTGIGFLDHMLDLFAKHALIDLTVEATGDLHVDDHHTTEDIGICLGQAIDQALGDRAGIRRYGHFTLPMDEVLVTAAVDMGGRYAFEYQAPISADKIGTFDTELVEHFWQSFAANAKCNLHVLMHYGRNAHHISEGIFKAVARAVRMAAESDPRSDAIPSTKGVL
>NZ_CP036262.1|WP_145352778.1|4670034_4671108_-|S-methyl-5-thioribose-1-phosphate-isomerase
MNSELVKTKASTLPPTLQWVGGIDGFLRLIDQTKLPVEEVYFDCNSVEQTHDAIYRLVVRGAPAIGIAAAYGVSVAIGTAMKEQADARKAALAAIDYLATSRPTAVNLFWALDQMRVVVNEATDQELADRVLQKAKAIHEQDRQTCAAIGQHGAPLLNGCRNVLTHCNAGALAASEKGTALAVIYAAHELQPELHVYADETRPLLQGARLTAWELARSGVDVTVLCDNMAASLMQAGKVDAVVVGADRIAANGDAANKIGTYPLAIVARHHGVPFYVAAPVSTFDRTLADGAGIPIEQRDAREVSHPYGTQTAADGANIYNPAFDVTPAELITAIITDQGIIQPVNAANVAKTIGLS
>NZ_CP036262.1|WP_145352779.1|4671147_4672584_-|dihydrolipoyl-dehydrogenase
MHTPLVVLGGGPGGYAAAFLAADEGLDVTIVEAEARLGGTCLLRGCIPSKALLHVARVISEVDELRADWGVRYDANPEIDVDAVRARKEKVIDNLTGGLANLAKRRKVTVIRARGSFIDSKTMKLEGDDPSIPEGGQLTFDHCILATGSVPAMPPAFDIGSDKVMDSTGALALADIPETLLVVGGGYIGLEMGSVYAGLGSKVTVVELSDGLLPGADRDLVKPLAKRIEKMVDGRLWLNTKVGSMAESEDGKVEVTFEGPGKFGHERFDRVLVSIGRRPVSRGLGLENTKVVVNERGFVECDSQQRTADPHILAIGDVAGDPMLAHKASHEGRVAAEVVAGKPSVFDKAAIPAVVFTDPEIAWAGLTEEEAKNAGRNYEVAVYPWAASGRAQALGRTEGLTKWLVDPDTKRVIGCGIVGAGAGELIAEAVLALEMGCEVGDIAETVHAHPTLGETLMNSAEVFFGTATEIYKPKRAKS
>NZ_CP036262.1|WP_145352780.1|4672708_4673317_-|30S-ribosomal-protein-S4
MARYTGPKARINRRLGALIYETSGASKALDRRPAPPGMHTRGRRPSNYGIALMEKQKIKHYYGLGERQLRRYFDAVSRRSGNTGELLLLMCESRLDNVVRRCGFAKTRPQARQGVVHGHFFVNGTKVAKPNYLLRPGDIIEVRNREKLKDVYRGVIANSSPDALDWVAFDSENLKATVQGLPGPSDISLPVDANAVVEFLSR
>NZ_CP036262.1|WP_145352781.1|4673726_4683449_+|hypothetical-protein
MFPKRSAPRVPASSRGQTARRRLAAALRPRRRLIRIEQLEDRRLLAVGTPVLGTSNDILFSGDATNDLMFFSVSEAGLLQHNRGGYFGFTSNSDLDSVTAGEQTRLVSELTSFRYEDAGSNDRLFFDGENPFSLGDAGIYASAGEITVRDDTSIESTGGVIQFVAAQKILLDQRSSLTTVDGGILLSGNPNADAIGDSIGLESVGATIRTSGSGNIQLVGFGGNDPAEYRNYGISLEEGTTIESTSETSSAGTIQIEGTGGDSSTAAYGVNIDGADIVVRSAYGDISIVGVGGHRSSASGSNFYGVNISAADVIESTGTGPDAATITIDGTGGAESRNNYGVRLAGATTDILSIDGDILIIGQGNGDGTGDTNYGVRSDSIGSIASTGTGIDAASITIIGEGGDGTRSGVGLSLNGSTTQLTSVYGDISIVGRGSDGSGYGNSGGSIGLTIASTGLGENAAKIDIQGTGGINTSGSGITVSGSITTTDGDVTITGLGTGDGTRSGDGGVNVTASIDAVGEADIIIDGTGGQGTGANHGVTISSGAALTTKDGEILITGQGSNGAGSNNYGVHIANIEGIESKWLSDGTIPSPAKITIDGTGGDTGGGNHGVYFDGASEGITSVDGAILITGRTGTGTGPSNVGVRMRDFGAIQSTGTTAHAATITIHGEGGFGQSNNYGVLIDSINRSSVSSFVGDILITGIGGTGDPDVSQSSNRGLVLSNVEIASLGTPDNATGTPATITINGTGGIADRQNYGTYINASAVKSVIGNIDIRGEGGGAGTGDTGVVISSTELVSSGEGDQAATITIHSESGVSGASLTLSTIDGDVSFTGLNGSSAYGTGVLTSTGDGMIRFDGGTVNAGSITSETSDIVLRGGAITVGTVESTGTGETAAKILIGDASTHSIQVNGDLTSVDGDIRIVNQITDPSTGVGSILLRGNITSTGINANHAASITIDGTGAENQVGVWFSGAGKSITSKVGDIEITGRGGASATGSSLHGVFLDRDVSISSTGTDTDAAQIDIHGTGGAGVNSNHGVYFRGDEEGSITSVVGAISITGTGGAGTGKSSAGVSIEEASISSTGISSASPAIDAATITITGIGGSGTSGNDGVYVGTDTAISSIDGAISIDGTGGDVGSGVILQYQSSLTSSGVGSDAASITVNGTAGLGAYGRGVSMSRNMVNSVDGDVTVEGYGSAGRSLGVYIDGSQVASTGTGVHAAEISILGIGGEEGSYDNYGVTVRRSTTSFTTIDGDLTIFGQGGSSGSTIGLRVETFDTIASTGTGPNAAKISLTGVLPDGTSGTAMTFAYGGRNLITSVEGDIALTVNANGSNGLFGPSGLVQIESTGVGADAAEISIESLGGEGGSISLSEGSRIDTVDGNIALNSARSIYVHGSISSTGTGIHAGQIRIDDSRAVSVSGSITSIDGDISVSSIKGDAPLSTGYVLMQGSIASTGVGTSAATITIEGQTKASMTSGVRIHGEVYSTDGDIQILGTGSGQYRSGVEVAYGGSVKSLGSDKAHAATITIDGSSGTEGGLGIQLLGETVDSSIVSTIAGDIRIIGDGGNGPQHANRGVWIRKGFVQSTGAASDNAGNITIEGSGGDGGTYDLVGVDISTDAKIVTVAGDIEIIAEAGVGSGSNNDGLRLGGVSLIGDASTAGDITIQADSIDLQSGTVQSTGLLTIAPGQAGTPIGIGGGAGDLNLSDAELALLVDGFNSITIGDATAGIIDIDTATFTDNVSLIGSAFHDHAGTDIDMGANTLSLIGTIAPGQSPGILRLAGAIEFADATVLDLEIDGPDADETANGHDQVSVTGTLIIGAGVTLQTATTNGFDPLLGQQLVIVENDETDPIEGEFAGLPEGSILTNFLGVPLDARISYLGLDGATGNDVVLTIIAGNLAPTADAGGPYFIDEGDSLTLDASLSSAPDDDPLDYTWDLNGDGDFSDAVGMTPMIPWSELDALGIGNVAQFTATVSVDDGRAAAVTATTTVNVQLNAPPIANAGESYEVGEGGSIQLNANGSTDDKGIENLTITWDLDGDGLFGETGIDAERGDETGAQPTFSATDVDGTKNVSVTVRVEDDRGKVDSDTTTVSVQNIAPTLILDSEVTIVRGDSITVEGSFVDPGPDTWTVTVDYADGTGQETLDLDGKKFDLDHEYNVAGTYLVVVTVDDGDGGVSSQNLKVIVNLPPLPDLTLISSDIRYLPINPAVGDPVNFVVDVTNAGSLAATDVPVRFMVYDAVSESFVEIGHTVIDSIDASPDSEGETSQSEVLFTWDGSAGQPPLPQEDVFLLVRVEVDAGSEIEELDESNNEDIQILQVGSPDFGTAAITANISDKTVYRNELVAVGGQAYYDFSTVPGDFDFPIQGASVTMRLLDPASGLVLAASTVLTASNGNFLHTIRSPELDGDYTLRFEVTEGTLSTVFESTLTVLGDSPEEPPSPPRSPPSRGYVFFPSIQFTQSVIPPGNPQIGEPVTIVGTFNYELAQPLLNVPVTFNDLFPVAGEVRTFEIGSGFVNFPDGGLEDPTLLPMDWTPTAEGFHIIQVIAEPDFNFRAHTHVTQLLLVGDLDTSSLTLAYELPTVVELPQLRAGARMFPIFAAAQAPQTPSPGDTVTYTIRYENTGDTTITGGQLIDDFDETVVGVPTNISDGGVVDGSVVRWELGDIPAGASGTVSYEVTINEAAELPPGSAFVFNTAVLNTDQAAAASTSELLLSNDSPVITNLNIEPMVAENGNVTLAGTFSDASLEDTHTIQITWGDGQTDTLLFTAGERAFSLPHSYDLTATPYVESYEIAVTLTDSSGQNSNGSVTTQTPVVAPPVPDEQSPNSSVASAVWNTETNLFDLLVDFADPPGGADAPVSGVQHLEVFYRVNPQNGNSAVQRFGDITLSPASPAGSQLLSRTIDAQPGDIIQVWSVATDGSGNVENEVTPRTDYSFAVADTVGPDTQVLSAIFDGNAFIDLHVSGVDVGGGHVDSIDVYVETRTGTASPIVSLIGTIPGGAAMVDETIKFAVPQDGVIRPYRFFSIGTDHLGNREGGNSLLDGDPGPEGDVLLSDIVLEEPSAAVVTGFDVNNGLENRSSVHSADILFNDENFIDQLLESLNDEDSSNDRIRIERLDLNGNSIEPPVYLPVTAVQDGLTLRLQFGATGIQENGVYAIRLDMDDDADNEWDDELQFHRLKGDINGDGAVDTSDLLKARLAYRNSALHADADVDGNGMVDAFDLRFFSTFLRQRDGEKVLGMPREELDD
>NZ_CP036262.1|WP_145352782.1|4683489_4684191_+|hypothetical-protein
MKTIKYLVPAILIATATLLDTSESQAGLLITISDAEVAPGESGYVDVLVSSNADALNPDSFDSFLLFFSVNVVDHPVAPINFLESIGTAPQLSATSPDYIFLGHSGLFFETISDSPGPPVANDFIDVIDATDDFSVSSISSGDSPFLLARLNFVSDPMATVGNFYEVSLDDAFFDGGNLPDFAVNSDARIYMVAAAVPEPSSLLIFTIAALAWTGHTRMRRSVKDKPRCVDNH
>NZ_CP036262.1|WP_145352783.1|4684755_4686000_+|NO-inducible-flavohemoprotein
MLSDKTIRIVKEITPLVAANAETITRRFYERMFEANPEVKAFFNQAHQHTGGQQKALAGAICAYFTHIDNPAVLMPAVEIIAQKHVSLGIKAEHYPIVGSNLLAAIKDVMGEGATDEIIEAVGEAYGFLADIFISRENAICEEQASAPGGWNGTRTFVVSKKIAESDIVTSFYLKPEDEGPLPPFKPGQYITVHIDHPHTPTSPRNYSLSDCASQPHYRISVKREERLSADAPDGLISNHLHDGIEEGHRIELGPPCGEFTIDPATVAKPVVLVAGGIGVTPLLSMAKSIIHANPNAPVYFIQAARNSKVQAFADELANLSDAGPNVHTKVIYDAPLPGDVEAGRCDDTGYVTTELLRGWTPFSEAEFYFCGPKPFMQNLHACLQELGVDEHRVRYEFFGPKEELQPAPSNVAG
>NZ_CP036262.1|WP_145352784.1|4686135_4686471_+|cupin-domain-containing-protein
MAINHANPAEVIHLQPLGSKIDSTKTYTLFKTDVMEAIRLVMPAGKQIPEHKARGEITVHCLEGAVKFFVGETPHELSAGDMLYLEAGKLHAVEAIEDSTVLVTIFLNKAS
>NZ_CP036262.1|WP_145355475.1|4686563_4687205_+|hypothetical-protein
MLQIDYCCGGDKPLENACWENGLEVLRVHSLLKQTVAETHDTEHPDWMHASLTELCDRIEQKHHARLKDSLPLLSRLMAEVVALHGEAHEELREVEQHFMTWRDEILTAMAEEERSLFPAIRQYDSEAFTDHSETLTAPLQEMIYRVRFEHADIGEALKKTRSASKNFLAPKDACAKFSQMYQLLRWTEADVRQYVHKEESILFPRVKKRLQG
>NZ_CP036262.1|WP_145352785.1|4687218_4687527_-|Rieske-2Fe-2S-domain-containing-protein
MPWIKAAKSQDVPVGTGKLVIVDDYLIALFNVDGVFYAIDDACPHQGAPLSDGRVEGCVAICPWHGAEFDVTTGKLLGGPGVRDVQAYAVKTKEDDVLIEVP
>NZ_CP036262.1|WP_145352786.1|4687532_4687985_-|hypothetical-protein
MMNQPNTIYDVLGMLADYHQQRAERYERLCKASVDPKADILLKHLVELETDSMNVVRDEMQRLPPEHSTYLLSGPRLSSEALHAVECNCKDESSFQEALSCALVSDQRLDELLDRIEDSTAAPSVIELAKRLREVEHMKGRQIAKFTRED

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Crispr_ID: NZ_CP036262_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_14

4775980-4776139

Orphan

Consensus_repeat	Method
AAGAAAGGTCCGTGCATTGTCTTCCTAGCGGTGCGGCGCGAGCCGCCCGGCCAAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_14

>merge|NZ_CP036262|14|4775980-4776139|CRISPRCasFinder
AAGAAAGGTCCGTGCATTGTCTTCCTAGCGGTGCGGCGCGAGCCGCCCGGCCAATTGCGCGATCCCACGCTTCCAAAAAGGCCGGACGGCTTGCGCCGTGCCGCTAAGAAAGGTCCGTGCACTGTCTTCCTAGCGGTGCGGCGCGAGCCGCCCGGCCAAT

>NZ_CP036262|14|12|4775980-4776139|CRISPRCasFinder
AAGAAAGGTCCGTGCATTGTCTTCCTAGCGGTGCGGCGCGAGCCGCCCGGCCAAT	TGCGCGATCCCACGCTTCCAAAAAGGCCGGACGGCTTGCGCCGTGCCGCT
AAGAAAGGTCCGTGCACTGTCTTCCTAGCGGTGCGGCGCGAGCCGCCCGGCCAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145352848.1\|4776223_4777273_-\|DUF4013-domain-containing-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352854.1\|4784162_4784804_-\|response-regulator	unknown	unknown	gnl\|CDD\|226932
NZ_CP036262.1\|WP_145352844.1\|4769969_4770959_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352852.1\|4781663_4782629_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145352856.1\|4786235_4786829_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224473
NZ_CP036262.1\|WP_145352841.1\|4767187_4768036_-\|type-III-pantothenate-kinase	unknown	unknown	gnl\|CDD\|224438
NZ_CP036262.1\|WP_145352850.1\|4779807_4780887_-\|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl\|CDD\|349906
NZ_CP036262.1\|WP_145352851.1\|4781014_4781434_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|379297
NZ_CP036262.1\|WP_145352857.1\|4786834_4788268_-\|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl\|CDD\|224062
NZ_CP036262.1\|WP_145352843.1\|4769589_4769850_-\|50S-ribosomal-protein-L27	unknown	unknown	gnl\|CDD\|235464
NZ_CP036262.1\|WP_145352849.1\|4778178_4779576_+\|PDZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|273938
NZ_CP036262.1\|WP_145352840.1\|4765400_4767140_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223021
NZ_CP036262.1\|WP_145352839.1\|4764296_4765349_-\|ferrochelatase	unknown	unknown	gnl\|CDD\|234585
NZ_CP036262.1\|WP_145352845.1\|4771090_4772533_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352846.1\|4773242_4774913_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|223642
NZ_CP036262.1\|WP_145352853.1\|4783011_4783299_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145352838.1\|4762334_4763624_+\|alkaline-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|366747
NZ_CP036262.1\|WP_145352855.1\|4785607_4785796_-\|carbon-storage-regulator-CsrA	unknown	unknown	gnl\|CDD\|376847
NZ_CP036262.1\|WP_145352847.1\|4775224_4775836_+\|superoxide-dismutase-family-protein	unknown	unknown	gnl\|CDD\|376292
NZ_CP036262.1\|WP_145352842.1\|4768032_4769190_-\|GTPase-ObgE	unknown	unknown	gnl\|CDD\|274271

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145352854.1\|4784162_4784804_-\|response-regulator	gnl\|CDD\|226932	COG4566, TtrR, Response regulator [Signal transduction mechanisms].	4.75881e-54
NZ_CP036262.1\|WP_145352852.1\|4781663_4782629_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	2.67069e-53
NZ_CP036262.1\|WP_145352856.1\|4786235_4786829_-\|hypothetical-protein	gnl\|CDD\|224473	COG1556, COG1556, Uncharacterized conserved protein [Function unknown].	2.35325e-11
NZ_CP036262.1\|WP_145352841.1\|4767187_4768036_-\|type-III-pantothenate-kinase	gnl\|CDD\|224438	COG1521, COG1521, Pantothenate kinase type III (Bvg accessory factor family protein) [Transcription].	8.83805e-27
NZ_CP036262.1\|WP_145352850.1\|4779807_4780887_-\|M20/M25/M40-family-metallo-hydrolase	gnl\|CDD\|349906	cd05656, M42_Frv, M42 Peptidase, endoglucanases. Peptidase M42 family, Frv (Frv Operon Protein; Endo-1 4-Beta-Glucanase; Cellulase Protein; Endoglucanase; Endo-1 4-Beta-Glucanase Homolog; Glucanase; EC. 3.2.1.4) subfamily. Frv is a co-catalytic metallopeptidase, found in archaea and bacteria, including Pyrococcus horikoshii tetrahedral shaped phTET1 (DAPPh1; FrvX; PhDAP aminopeptidase; PhTET aminopeptidase; deblocking aminopeptidase), phTET2 (DAPPh2) and phTET3 (DAPPh3), Haloarcula marismortui TET (HmTET) as well as Bacillus subtilis YsdC. All of these exhibit aminopeptidase and deblocking activities. The HmTET is a broad substrate aminopeptidase capable of degrading large peptides. PhTET2, which shares 24% identity with HmTET, is a cobalt-activated peptidase and possibly a deblocking aminopeptidase, assembled as a 12-subunit tetrahedral dodecamer, while PhTET1 can be alternatively assembled as a tetrahedral dodecamer or as an octahedral tetracosameric structure. The active site in such a self-compartmentalized complex is located on the inside such that substrate sizes are limited, indicating function as possible peptide scavengers. PhTET2 cleaves polypeptides by a nonprocessive mechanism, preferring N-terminal hydrophobic or uncharged polar amino acids. Streptococcus pneumoniae PepA (SpPepA) also forms dodecamer with tetrahedral architecture, and exhibits selective substrate specificity to acidic amino acids with the preference to glutamic acid, with the substrate binding S1 pocket containing an Arg allows electrostatic interactions with the N-terminal acidic residue in the substrate. The YsdC gene is conserved in a number of thermophiles, archaea and pathogenic bacterial species; the closest structural homolog is Thermotoga maritima FrwX (34% identity), which is annotated as either a cellulase or an endoglucanase, and is possibly involved in polysaccharide biosynthesis or degradation.	3.65544e-136
NZ_CP036262.1\|WP_145352851.1\|4781014_4781434_-\|carboxypeptidase-regulatory-like-domain-containing-protein	gnl\|CDD\|379297	pfam13620, CarboxypepD_reg, Carboxypeptidase regulatory-like domain.	0.00195302
NZ_CP036262.1\|WP_145352857.1\|4786834_4788268_-\|4Fe-4S-dicluster-domain-containing-protein	gnl\|CDD\|224062	COG1139, COG1139, Uncharacterized conserved protein containing a ferredoxin-like domain [Energy production and conversion].	1.19619e-163
NZ_CP036262.1\|WP_145352843.1\|4769589_4769850_-\|50S-ribosomal-protein-L27	gnl\|CDD\|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	1.31752e-47
NZ_CP036262.1\|WP_145352840.1\|4765400_4767140_-\|hypothetical-protein	gnl\|CDD\|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	0.000268596
NZ_CP036262.1\|WP_145352855.1\|4785607_4785796_-\|carbon-storage-regulator-CsrA	gnl\|CDD\|376847	pfam02599, CsrA, Global regulator protein family. This is a family of global regulator proteins. This protein is a RNA-binding protein and a global regulator of carbohydrate metabolism genes facilitating mRNA decay. In E. coli CsrA binds the CsrB RNA molecule to form the Csr regulatory system which has a strong negative regulatory effect on glycogen biosynthesis, glyconeogenesis and glycogen catabolism and a positive regulatory effect on glycolysis. In other bacteria such as Erwinia caratovara RmsA has been shown to regulate the production of virulence determinants, such extracellular enzymes. RmsA binds to RmsB regulatory RNA.	9.3408e-23
NZ_CP036262.1\|WP_145352839.1\|4764296_4765349_-\|ferrochelatase	gnl\|CDD\|234585	PRK00035, hemH, ferrochelatase; Reviewed.	2.28601e-125
NZ_CP036262.1\|WP_145352846.1\|4773242_4774913_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|223642	COG0568, RpoD, DNA-directed RNA polymerase, sigma subunit (sigma70/sigma32) [Transcription].	1.34598e-31
NZ_CP036262.1\|WP_145352838.1\|4762334_4763624_+\|alkaline-phosphatase-family-protein	gnl\|CDD\|366747	pfam01663, Phosphodiest, Type I phosphodiesterase / nucleotide pyrophosphatase. This family consists of phosphodiesterases, including human plasma-cell membrane glycoprotein PC-1 / alkaline phosphodiesterase i / nucleotide pyrophosphatase (nppase). These enzymes catalyze the cleavage of phosphodiester and phosphosulfate bonds in NAD, deoxynucleotides and nucleotide sugars. Also in this family is ATX an autotaxin, tumor cell motility-stimulating protein which exhibits type I phosphodiesterases activity. The alignment encompasses the active site. Also present with in this family is 60-kDa Ca2+-ATPase form F. odoratum.	1.28348e-54
NZ_CP036262.1\|WP_145352842.1\|4768032_4769190_-\|GTPase-ObgE	gnl\|CDD\|274271	TIGR02729, Obg_CgtA, Obg family GTPase CgtA. This model describes a univeral, mostly one-gene-per-genome GTP-binding protein that associates with ribosomal subunits and appears to play a role in ribosomal RNA maturation. This GTPase, related to the nucleolar protein Obg, is designated CgtA in bacteria. Mutations in this gene are pleiotropic, but it appears that effects on cellular functions such as chromosome partition may be secondary to the effect on ribosome structure. Recent work done in Vibrio cholerae shows an essential role in the stringent response, in which RelA-dependent ability to synthesize the alarmone ppGpp is required for deletion of this GTPase to be lethal. [Protein synthesis, Other].	4.33169e-180
NZ_CP036262.1\|WP_145352847.1\|4775224_4775836_+\|superoxide-dismutase-family-protein	gnl\|CDD\|376292	pfam00080, Sod_Cu, Copper/zinc superoxide dismutase (SODC). superoxide dismutases (SODs) catalyze the conversion of superoxide radicals to hydrogen peroxide and molecular oxygen. Three evolutionarily distinct families of SODs are known, of which the copper/zinc-binding family is one. Defects in the human SOD1 gene cause familial amyotrophic lateral sclerosis (Lou Gehrig's disease). Structure is an eight-stranded beta sandwich, similar to the immunoglobulin fold.	1.5345e-39
NZ_CP036262.1\|WP_145352849.1\|4778178_4779576_+\|PDZ-domain-containing-protein	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	1.09295e-88

>NZ_CP036262.1|WP_145352847.1|4775224_4775836_+|superoxide-dismutase-family-protein
MIRTKPFALAVAFATCFAFSSASAQDKPAHSHEKESHHGHAEAGHHHGDLPTFGVAIVTPTKGNKVRGVLQLKQVGDDLKVMGKVRNLTPGKHGFHIHEFGDFRDGAKGTSAGGHFNPAGVDHGPEGHGHVGDLGNITANDEGVATIKTTLKNTKLHFVLGRSFVIHADADDLKSQPSGNAGPRVGLGIIGIGNAEYKPAAKK
>NZ_CP036262.1|WP_145352846.1|4773242_4774913_+|sigma-70-family-RNA-polymerase-sigma-factor
MHEEYRDENIKQLRDQQVRFAPRAKKLEQAMRAEQLLADLEDSRSYSFDFVCFRITDYRPELSQRRNIKGADLKYDLRLFVEDMSEAADITIEEANESVHTVGDLSRMFSVSTKTISRWRDQGLVSRRFVVGGRKRVGFLQSSVERFVAKNGARIRRGERFSQLSDEEKGEIIERARQLAESGASLSEVTRCLAEQMHRSPETVRYTLKNYDAENASLAIFPNHRGTLTEEDKRSIFQQFHRGSTVNQLCKRYGRTRSSITRILVDVRVARTMELPLDYMYNEDFEDASREPEFLGEMPALDPASRRQRVPADLPPYLAALYDVPLLNREQEYHLFRKMNYLKHKASQLREQLQNSADRAAVMEQIHDLYEQAVAVKNKIVQSNLRLVVSIAKRHMNSTDDFFALVSDGNMSLIRAAEKFDYGRGNKFSTYATWAIMKNFARTIPSEFKHRDRFRTTAEELFLAQSDNRGNPFVEESTQRQRQREVGRILNRLDEREQKIISARFGLAKGSEPLTLKEVGQEMGVTKERIRQLEARALNKLREAASEAKIDVELGS
>NZ_CP036262.1|WP_145352845.1|4771090_4772533_-|hypothetical-protein
MKRRNFLLNGLAVASLAGGLRKASYAAPSDEQYLFTPVLHPTCRVRIEMELKGNIDLAKNELVSKERVRQLPIAYDSVLDYEERLSVKDDQKPRGARRYYHTAMSQGTTSGTPSRLELRDSAKHTAVHLTEGRSVSYAASAYLTHEEVSLLEIPVNSLVIDQALPTEPLAIGAEYKLDTEILRQLLDMDAIQEQDVVSKLVSVDDKSARFEWTGTVQGSTDGVPTVIDLAGKITFDRKAKFCSWVAIALRERRQIGKAKPGFELSATIKVLRKPLTDVVTVLDKPLGDTPKPAQLLVNLYSTAGRYGVLMDRRWQMISQSSSLSTMRMVDQDRDIAQCDVRHLPSLDAGRQLTLEALQADIKKSLGEQFREWISASELANGSDLRIARAHAMGVAEGVPVHWVFAHCSDDSGRRILATFTLAADNQEAFAGADEQFVQSLRFLTVASPSTDEEQEEEGDAAAKPDTQAASRPTSAAKTQR
>NZ_CP036262.1|WP_145352844.1|4769969_4770959_-|hypothetical-protein
MKSNLFIVAAGLLLALTVQPILSGQDSKLPAVRVESTLFAPGTVTIIPPQPTAEETFTGPIALRDFIDAHPEIAWKAPEFKDGRPYSDPRTRTLPEMARQVILRREVYSLEFAFKPLRQIYADVPQPDGRMKRKLIWYMVFRVRYLGGDLRAAEDSSSNTPYGRIEAVSYKSRRFLPLIVLSNHVTGKEYLDRILPAVKDVIATREKITAPLYNTVEISSQPIKLATDPSSPGVWGLATWEDVDPEIDFFSVYVSGLTNAFKREESKDNKVTLLKKTLQLNFYRPGDTMRQTDDEIRFGIPAFSNAKEQKEILDEYGLTKRLDYQWVYR
>NZ_CP036262.1|WP_145352843.1|4769589_4769850_-|50S-ribosomal-protein-L27
MAHKKGQGSSRNGRDSNAQRRGVKRFGGQKVTPGSILVRQVGTKFHPGANVGMGNDYTLFALTEGVVRFDRKGRRINVDAVAVEAA
>NZ_CP036262.1|WP_145352842.1|4768032_4769190_-|GTPase-ObgE
MFVDRVEIEVHAGKGGDGCASFRREIYIPKGGPDGGNGGHGGSITLTAVAGVNSLSAFQGRYYWRAPKGMPGQGADCHGRRGKDMPLQVPPGTAVIDAEHGFVIKDLIEPGDSIVIARGGKGGYGNTHFKSSTNQAPRQFQRGELGESRKVILELKSIADVGLVGKPNAGKSTLLSRLSKARPEIADYPFTTKHPNLGMVRANAERSFVLADIPGLIDGASEGVGLGHEFLRHVERAGILLHLVEPEPNDQTDPLQNYISIRGELDAYSEDLAGRPEIVAVTKAELPSSQEAQVALQEHLGHPVYRISAVTGEGLNELLRTVTKALDEARPEGTPSLLLSETDRPQEPDEPAPEKPRRVPPHLAGPTAQLCDDLQAKDVPGEGTK
>NZ_CP036262.1|WP_145352841.1|4767187_4768036_-|type-III-pantothenate-kinase
MSQDPVESLCIGVDLGNTRVKCWALGAAADWQQGLSLADQQAIRSAAWLDRVMQWRDQLVHSLPIASAQPAVEWVIASVQATITGRFCDRITSHFPSDRFRVLSSADVPLRTRLPARQKIGIDRLLTSWVAWQNNRRGEPGPTIVADAGSALTIDWTGVEGEFRGGAILPGVQLQLQSLGEHIPALSAAVESIIQQHLSPQPATSVPSFPGMDTESAIAVGVYTSAAAAIDRFVQQVELESATRVQLWLTGGDAPRIAPWLKSQYRLEPDLMRDAINRLIYV
>NZ_CP036262.1|WP_145352840.1|4765400_4767140_-|hypothetical-protein
MAESLAELLGIDPNTEKPNAYQIFGLQAGESDPERIEQAIGGVVRRLKENQAATEPALWSRAATAVTKARRLLIDPESRAAYDAKLRQSRKRRSAPISEADSDPLAGLLPKSDPLAPFDIEAAAARSAGLRPRQPPPLPTSVHSIDDTPEFADALTDTVDPDDQEPGGSGLGMAGLSDPAVEPAQVESPQAESPAVESIQFDPTVSMLQAGTANPSSGDNGNAGSGGDMAFAQLASAPKSSVRRRRTSRAPMILLSAVVLLMLGGIGGAAYYLVERESQLTTQPQVAQAAAPVPRDRPRAQPSDSIMGSMGPRKSTKPPADLAPFETSNQPMPSAMPMAAGNGMGAGMETPSQPDMQEPSMPMQPEVTPDLSVASLPKPPMPTPTPPPAPPAPSDAEIKQGDAALLAAQNAFLKRNWLQVKPLAENAQRQAKTAAQIAAADKWFEVAEMADYYLGGIKKALGDLKSGNTLQLAPTLEVAISEVSQDHLKLQVNGRIKRYTFEEIPLLVLHQLEKMTMSAGEPAAPVARAVYQYWTPVSKPADREEALEQLRAMPDEVGGVHPHEIADTLQALPAATPSS
>NZ_CP036262.1|WP_145352839.1|4764296_4765349_-|ferrochelatase
MHETTSATSYDSFLLVSFGGPEGPDDVLPFLENVLRGKPVPRERMLEVAEHYRSFGGVSPINSQNRLLLEALKLEFEQRGIELPIYWGNRNWHPMLSDTLQQMKTDGCSRTLAFFTNMFSSYSGCRQYRENLAEACRTVGEDAPQIDKLRFGFNHPKFIQTVARNLKDSLEELQADPATTKVLFTAHSIPMSMADHCDYERQLKEASRLVAENVGNQNWELVYQSRSGSPHQPWLEPDVCDWIAEADDREKLERLVVVPLGFVSDHMEVIYDLDHEAADLCKERGIAFSRSKTVGVDPQFVSMIADLIIERQSGEVERVAIGDLGPWHDVCPADCCQYNPTRPTRPSESK
>NZ_CP036262.1|WP_145352838.1|4762334_4763624_+|alkaline-phosphatase-family-protein
MTSKIVVINVVGLTPELLQHAPRISQAGSAKPLRGPLPAVTSTAQATILTGLNPAEHGIVGNGWYFRETGEIRFWQQANTLIQGETLYQAISPAKTAKMFWWYNQGAPVEWSATPKPHYGCDGSKEFGILDRTSCELVKNLGPFPFHAFWGPFSGVASSQWIAAASAKVIEQKRPELTLVYLPHLDYDYQRFTEHDPQRVAEVDACAGTVIDAAERIRAEVIILSEYGLVPVSRPVMINQALREAGLLTVRDGPFGEMLMPMDSKAFAVVDHQLAHIYVSDRSLLPAVRDCLESLPGVDAVVDPCDIGLGHPRSGELVALSEPDAWFCYYYWLDDRKAPDFARTVDIHRKPGYDPCELFITSKFRAAARLAQKKLGMRYRMDVVPLDPRLVRGSHGLRTAPQKGAVIVGQDPPEDMLQVKDYVRSRMER
>NZ_CP036262.1|WP_145352848.1|4776223_4777273_-|DUF4013-domain-containing-protein
MSVLLALLAAIPALQWITFGYMLEVSGRLSRGEKLRDSFPWSDVATRIGFALAAIFLVSLPVHLLTHWSQVARLIDPESNASLPLRWLGGFAVGAAGIYLSWAWMRGGRLRDYLWPAPIRFLKTYWRPSTWLAARDDLWSLLVSLEVPRLFWLGVRGAVGTLVWIIVPAILLIVANREGKGGSAGVLGALAFVAMGIVLMYVPLLQSRFAEKNRLTEMFNVAAVRRSYRRAPWAHTFAALLLFGLAIPLYLLKIETLPREATWLPCLMFVALMLPARTVLGLATRRSNHRPEPQGWWAGIQRWMARGLMPAIVGIYMLFVFLSQYLDVHGLQTWFHQHAILVPVPFTGT
>NZ_CP036262.1|WP_145352849.1|4778178_4779576_+|PDZ-domain-containing-protein
MSDSITGASYMLYDTKITVSRPTPRLLLAAALVFTLLASPTALGDSPRETSVVRAYRAASPSVVNIHGQKTIRSTTAGFNGSSAESFRQVNGMGTGVIVDPRGYIITNFHVIEDVADIRVTLKDGRTVSASTISHNRANDLAVIKINVSEPLPVIARTSSEDLMVGEPVLAIGNAFGYENTLTQGIISALHRDVPVNETQSYRDLIQTSAGINPGNSGGPLLNIEGKMIGINVAVRVGAQQIAFTIPVDQALETVAIMLEERNRKQVSLGVEELLAPGTQSLQIEHPLSTQLEPGDKITKVANKEVQTRFDFALAATEVRPGDSVPMQITRNGVKKEFTLVAGDPSTSNFGARTADLVWQWIGIRTEPLSSAELRRLNQRTATPNQGGLKITSLRSGSPAAHQGIEPGDILLGIHEWRTASLDDLEMIIDHPELQRAPETRFYILRSNKTLYGYMRLADRPVARR
>NZ_CP036262.1|WP_145352850.1|4779807_4780887_-|M20/M25/M40-family-metallo-hydrolase
MAIEPAARQFLMDALATPSPSGYEEKVQAVVRQYIEPVAESVRIDVHGNLMASSVPGDGPRLMYAGHCDQIGMLVSYIDDEGFVYANTIGGWDPQQLIGQTMTIWTDHGPLPAVISRKPIHLLSTSERTEVVKIEQMWLDIGACDKAEAEKHVRIGDPITLHLNHRALLGAHLSGPAMDNTTGMWTVMEAFRRAAVSKSELRCQLTSVSTVQEEIGLRGAKTAAGSIRPDVAIAVDVTHASDCPTIDKTQRGDIRLGRGPVIARGPNMNPRVVARLIELAERNGIPYQVAAIGRATPNDANVLQIHGGGVATGLVAIPNRYMHSAVETISTEDIDNAAELLSHFALELSADDDFTPCVG
>NZ_CP036262.1|WP_145352851.1|4781014_4781434_-|carboxypeptidase-regulatory-like-domain-containing-protein
MIRIKRTAVVMIALCSSALPLLSGCTPSTGFYEVEGTVTHNGEPVPKVFLIFHPANPDIHPEAMAMSDEQGRYKMMVGNSPGVPPGEHTVYATDPAAVQGGSSSDDPDYKEVITKYGPGTSTYKVTIDKDESELELKLD
>NZ_CP036262.1|WP_145352852.1|4781663_4782629_-|DUF1559-domain-containing-protein
MRTYLGRHRVGFTLVELLVVIAIIGVLVGLLLPAVQAAREAARRMSCSNNMKNMALAVHNYHDTHKKFPAGNIAWNGLGTNSTRAQANSEPNGRWYNGMWAWPVAILPFMEGQNLYDQMDFNQLPYTPERGDVYFGDYGPETNHGVVNELPCTSAPAAFRCPSVPLIGDEGAFKDYAGNSGGTRMSTCCPERATDTDGIFHKNKNYTFGSIIDGSSNTLLFVEQSNFIQGHNRPTNPFVWMNHSSQGESISHQGGNSFPPNLPKAIVIDAWRVTGRLARGMHPSGIMVAYCDGSVGFVSETISVNNWRAIHSRDAGEVVQN
>NZ_CP036262.1|WP_145352853.1|4783011_4783299_-|hypothetical-protein
MLKNPAVCRTGSRRIVMFFEPRVAGFLNDVNLPNSPPENFSGLPVRFTQPEPTTSASSRTFFFASLRCIPTFRIVRKISDLPVKLRIGAKEMRGI
>NZ_CP036262.1|WP_145352854.1|4784162_4784804_-|response-regulator
MPDQTTQDTFPADPIVFVVDDEASSRNVIAEMVKSMSLPVESYDSAEAFLATYRNQRPACIVTDQRMPGMSGIDLIEKLQEQDLTIPVIVVTAFPDTQSTVRAVRGGAISLIEKPCRREKLWTMIVEAIRLDKRNSVKDAEREHAKQCVESLNEGERAVAHMLIEGLANKVIAARLDVSLRTVESRRAAIFKKFGVTSIASMVLLWLTAHPDS
>NZ_CP036262.1|WP_145352855.1|4785607_4785796_-|carbon-storage-regulator-CsrA
MLVLSRKKNESIVINNDIKIVVVEIRGDKVRLGVEAPREVPVHRREVYDAIQRSKEDAPEQV
>NZ_CP036262.1|WP_145352856.1|4786235_4786829_-|hypothetical-protein
MTSSSRQSILDRVRSRSLPEAPLPELDHDRLIRFDDLADAFQHSAESVGATVIRCRSIDEVPEHLLKIDSFREADEFASTIEKIPGNVQVSSRTSGHDWASLDWLLIQSRLGVAENGAVWVPTQELNNRVQVFITQHLGVVLKAEDLVHHMHGAYESIGAIERYGVFVSGPSKTADIEQSLVLGAHGCRTLTLFLLV
>NZ_CP036262.1|WP_145352857.1|4786834_4788268_-|4Fe-4S-dicluster-domain-containing-protein
MKSTVDHPTAAKPFVANQERMKWHDGALWFVREKRDRQAHSIPEWEYLRELASQTKAHTQANLAEYLEAFERQATAAGAVVHWAADAEEHNAIVLGLLQKNNVQRVVKSKSMLTEECHLNPYLEAQGIEVVDTDLGERIIQLRDEPPSHIVLPAIHLKKGDVGETFHEHLGTEKGASDPKYLTEAARQHLRDRFLNAQAGITGVNFAIAETGGVTVCTNEGNADLGASLPPLHIACMGIEKLIPRQADLGIFLRLLARSATGQPITTYSSHFLGPREGGQLHIVLVDNGRSSIRDRDEFREALNCIRCGACMNTCPVYRRSGGHSYASVVPGPIGSVLSPAADTEQHKSLPFACSLCGSCTDVCPVKIPLHHQLLAWRQEIGREGLLPVSKRMPMKAAAALFARPRLFAVAGWFGRFALRVLPHALTHNRLNTWAVARELPIAPKKSFRSWYRDQDRPANSLPIVTPDPESSPTKNR

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Crispr_ID: NZ_CP036262_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_15

5147520-5147813

Orphan

Consensus_repeat	Method
TGGGGAGCANGGTGGNGAGCANGGTGGNGA	CRT

5 spacers

The CRISPR arrays of NZ_CP036262_15

>merge|NZ_CP036262|15|5147520-5147813|CRT
TGGGGAGCAAGGTGGGGAGCAAGGTGGGGAGCAAGGTGGGGAGCAAGGTGGGGAGCAAGGTGGGGAGCAAGGTGGAGAGCAAGGTGGAGAGCAAGGTGGAGAGCAGGGTGGGGAGCAAGGTGGAGAGCAGGGTGGAGAACAGGGTGGGGAACAGAGTGGGGAGCAAGGTGGAGAGCAGGGTGGGGAACAGGGTGGAGAACAGGGTGGTGAGCAGGGTGGGGAGCAGGGTGGAGAACAGGGTGGAGAGCAGGGTGGAGAGAAAGGTGGGGAACAGGGTGGTGAGCAGGGTGAGGG

>NZ_CP036262|15|1|5147520-5147813|CRT
TGGGGAGCAAGGTGGGGAGCAAGGTGGGGA	GCAAGGTGGGGAGCAAGG
TGGGGAGCAAGGTGGGGAGCAAGGTGGAGA	GCAAGGTGGAGAGCAAGGTGGAGAGCAGGG
TGGGGAGCAAGGTGGAGAGCAGGGTGGAGA	ACAGGGTGGGGAACAGAG
TGGGGAGCAAGGTGGAGAGCAGGGTGGGGA	ACAGGGTGGAGAACAGGGTGGTGAGCAGGG
TGGGGAGCAGGGTGGAGAACAGGGTGGAGA	GCAGGGTGGAGAGAAAGG
TGGGGAACAGGGTGGTGAGCAGGGTGAGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145353208.1\|5156333_5156927_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145353189.1\|5141343_5142219_-\|NAD(P)H-hydrate-dehydratase	unknown	unknown	gnl\|CDD\|238576
NZ_CP036262.1\|WP_145353200.1\|5150269_5151127_-\|TIGR03546-family-protein	unknown	unknown	gnl\|CDD\|200289
NZ_CP036262.1\|WP_145353213.1\|5159387_5160797_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036262.1\|WP_145353204.1\|5152143_5153175_+\|nucleotide-pyrophosphatase	unknown	unknown	gnl\|CDD\|293742
NZ_CP036262.1\|WP_145353181.1\|5138175_5138574_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238219
NZ_CP036262.1\|WP_145353198.1\|5148515_5150273_-\|TIGR03545-family-protein	unknown	unknown	gnl\|CDD\|274640
NZ_CP036262.1\|WP_145353191.1\|5142212_5144009_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|236848
NZ_CP036262.1\|WP_145353193.1\|5144287_5145967_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236090
NZ_CP036262.1\|WP_145355566.1\|5155161_5156247_+\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145353206.1\|5153658_5154801_-\|acyltransferase-family-protein	unknown	unknown	gnl\|CDD\|376607
NZ_CP036262.1\|WP_145353195.1\|5145974_5146490_+\|GrpB-family-protein	unknown	unknown	gnl\|CDD\|377252
NZ_CP036262.1\|WP_145353179.1\|5136681_5137722_-\|3-deoxy-7-phosphoheptulonate-synthase	unknown	unknown	gnl\|CDD\|181535
NZ_CP036262.1\|WP_145353185.1\|5139363_5139924_+\|DJ-1/PfpI-family-protein	unknown	unknown	gnl\|CDD\|153243
NZ_CP036262.1\|WP_145353187.1\|5140236_5141310_-\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|224871
NZ_CP036262.1\|WP_145353214.1\|5160816_5162505_-\|flagellar-hook-associated-protein-FlgK	unknown	unknown	gnl\|CDD\|224176
NZ_CP036262.1\|WP_145353183.1\|5138577_5139354_+\|sirohydrochlorin-chelatase	unknown	unknown	gnl\|CDD\|225049
NZ_CP036262.1\|WP_145353210.1\|5157107_5159225_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224001
NZ_CP036262.1\|WP_145353177.1\|5135929_5136685_-\|triose-phosphate-isomerase	unknown	unknown	gnl\|CDD\|234589
NZ_CP036262.1\|WP_145353202.1\|5151193_5152081_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145353189.1\|5141343_5142219_-\|NAD(P)H-hydrate-dehydratase	gnl\|CDD\|238576	cd01171, YXKO-related, B.subtilis YXKO protein of unknown function and related proteins. Based on the conservation of the ATP binding site, the substrate binding site and the Mg2+binding site and structural homology this group is a member of the ribokinase-like superfamily.	3.46699e-82
NZ_CP036262.1\|WP_145353200.1\|5150269_5151127_-\|TIGR03546-family-protein	gnl\|CDD\|200289	TIGR03546, TIGR03546, TIGR03546 family protein. Members of this family are uncharacterized proteins, usually encoded by a gene adjacent to a member of family TIGR03545, which is also uncharacterized.	1.66609e-35
NZ_CP036262.1\|WP_145353213.1\|5159387_5160797_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	4.3305e-52
NZ_CP036262.1\|WP_145353204.1\|5152143_5153175_+\|nucleotide-pyrophosphatase	gnl\|CDD\|293742	cd16018, Enpp, Ectonucleotide pyrophosphatase/phosphodiesterase, also called autotaxin. Ecto-nucleotide pyrophosphatases/phosphodiesterases (ENPPs) hydrolyze 5'-phosphodiester bonds in nucleotides and their derivatives, resulting in the release of 5'-nucleotide monophosphates. ENPPs have multiple physiological roles, including nucleotide recycling, modulation of purinergic receptor signaling, regulation of extracellular pyrophosphate levels, stimulation of cell motility, and possible roles in regulation of insulin receptor (IR) signaling and activity of ecto-kinases. The eukaryotic ENPP family contains at least five members that have different tissue distribution and physiological roles.	3.49566e-24
NZ_CP036262.1\|WP_145353181.1\|5138175_5138574_+\|hypothetical-protein	gnl\|CDD\|238219	cd00371, HMA, Heavy-metal-associated domain (HMA) is a conserved domain of approximately 30 amino acid residues found in a number of proteins that transport or detoxify heavy metals, for example, the CPx-type heavy metal ATPases and copper chaperones. HMA domain contains two cysteine residues that are important in binding and transfer of metal ions, such as copper, cadmium, cobalt and zinc. In the case of copper, stoichiometry of binding is one Cu+ ion per binding domain. Repeats of the HMA domain in copper chaperone has been associated with Menkes/Wilson disease due to binding of multiple copper ions.	0.00763294
NZ_CP036262.1\|WP_145353198.1\|5148515_5150273_-\|TIGR03545-family-protein	gnl\|CDD\|274640	TIGR03545, TIGR03545, TIGR03545 family protein. This model represents a relatively rare but broadly distributed uncharacterized protein family, distributed in 1-2 percent of bacterial genomes, all of which have outer membranes. In many of these genomes, it is part of a two-gene pair.	1.32545e-80
NZ_CP036262.1\|WP_145353191.1\|5142212_5144009_-\|HAMP-domain-containing-protein	gnl\|CDD\|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	4.15226e-66
NZ_CP036262.1\|WP_145353193.1\|5144287_5145967_+\|hypothetical-protein	gnl\|CDD\|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	3.03186e-12
NZ_CP036262.1\|WP_145355566.1\|5155161_5156247_+\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	1.75593e-54
NZ_CP036262.1\|WP_145353206.1\|5153658_5154801_-\|acyltransferase-family-protein	gnl\|CDD\|376607	pfam01757, Acyl_transf_3, Acyltransferase family. This family includes a range of acyltransferase enzymes. This domain is found in many as yet uncharacterized C. elegans proteins and it is approximately 300 amino acids long.	2.61554e-13
NZ_CP036262.1\|WP_145353195.1\|5145974_5146490_+\|GrpB-family-protein	gnl\|CDD\|377252	pfam04229, GrpB, GrpB protein. This family has been suggested to belong to the nucleotidyltransferase superfamily. It occurs at the C-terminus of dephospho-CoA kinase (CoaE) in a number of cases, where it plays a role in the proper folding of the enzyme.	2.40328e-36
NZ_CP036262.1\|WP_145353179.1\|5136681_5137722_-\|3-deoxy-7-phosphoheptulonate-synthase	gnl\|CDD\|181535	PRK08673, PRK08673, 3-deoxy-7-phosphoheptulonate synthase; Reviewed.	0
NZ_CP036262.1\|WP_145353185.1\|5139363_5139924_+\|DJ-1/PfpI-family-protein	gnl\|CDD\|153243	cd03169, GATase1_PfpI_1, 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.	9.4856e-83
NZ_CP036262.1\|WP_145353187.1\|5140236_5141310_-\|acyl-CoA-dehydrogenase	gnl\|CDD\|224871	COG1960, CaiA, Acyl-CoA dehydrogenases [Lipid metabolism].	4.65963e-20
NZ_CP036262.1\|WP_145353214.1\|5160816_5162505_-\|flagellar-hook-associated-protein-FlgK	gnl\|CDD\|224176	COG1256, FlgK, Flagellar hook-associated protein [Cell motility and secretion].	2.10087e-70
NZ_CP036262.1\|WP_145353183.1\|5138577_5139354_+\|sirohydrochlorin-chelatase	gnl\|CDD\|225049	COG2138, COG2138, Sirohydrochlorin ferrochelatase [Inorganic ion transport and metabolism].	1.83711e-33
NZ_CP036262.1\|WP_145353210.1\|5157107_5159225_-\|hypothetical-protein	gnl\|CDD\|224001	COG1075, LipA, Predicted acetyltransferases and hydrolases with the alpha/beta hydrolase fold [General function prediction only].	8.7809e-07
NZ_CP036262.1\|WP_145353177.1\|5135929_5136685_-\|triose-phosphate-isomerase	gnl\|CDD\|234589	PRK00042, tpiA, triosephosphate isomerase; Provisional.	3.89972e-139

>NZ_CP036262.1|WP_145353195.1|5145974_5146490_+|GrpB-family-protein
MSLPVRLSHYDPSWRQEFEQTRSSILMSCSGWVQSVEHIGGTAIPGLIAQAIVDCVAGVVAPEGLEAASTAIEGLNYRREKLPTWVDDGILFTKPRHGPTTHRIFLTRIDSPLWSRVLRVRDWLREHPEVAYRFEDAKVKQWKAAGGDPCRYAHAKAIFFAHLEDQIHTTG
>NZ_CP036262.1|WP_145353193.1|5144287_5145967_+|hypothetical-protein
MSRKSRRFLQASIVGPLVLVLSVSPASAGWLKKHLHCAPPPCPPVNCVPVCPPAPVCCDPVPVECVPVVPDCCGSVPVYAEPMHLEPTPLEHHPSEESLKPATDETAPAPSDEVFDAAPPSLPAEEKAPAEEVTAPAPKEAAPAPAPEPKEAAPEPKEAAPEPKEAAPEPKEAAPAVEEAAPAEDIFGAPVEEAAPAMEAPAAEPAPAGDDIFGAPAEEAAPAGDDIFGAPVEEAAPAMEAPAAEAAPAGNDIFGAPAEEAAPAGDDIFGAPVEEAAPAMEAPAEEAAPAGNDIFGAPAEEAAPAGDDIFGAPVEEAAPAMEAPAAEAAPAGDDIFGAPAEEAAPAGDDIFGAPAADAPAMEAPAAGDDIFGAPASDAPAAGDDIFGAPPADAPAMEAPAAGDDIFGAPPAGDDIFGAPPADAPAMEAPAAGDDIFGAPPAEAAEDDIFGAPSAEAPAAEPLDNDIFGAAPATEPAEVAVHAAVNVMDTTEMRVWIDNTGGFSTTGRLIEIQDDFVRLQKENGRTCTVPARRLSPADSAYVESIANQLPSETIAMLINN
>NZ_CP036262.1|WP_145353191.1|5142212_5144009_-|HAMP-domain-containing-protein
MIRLLQNAFASMSLERKSVLLFVSALVPLMLAAFWVVQLLAGKLVIDRTRQVARDFGAAKLMRVHCDAIYGVELSPDVRKTSLEVLNDLELKLLRPEYEYAVLSLGEETTYDNLTDATQPDDETERELLEQLRDKFYLRLEQYLAKDRPDLVQRPMLLEENEAFTQIAPGRQPLSLERGPIDGRYIHYTPVFSEPECLVSCHSPKVPVSFAPDADPKLLAQQYPFRVIRVSMPYNATQEANNWIRAVVIAVAMLIIAITVVVLHRIMRYLVLHPLYHLRDVSDAITHGDTNLRASIDTEDEFRELANAFNRMLRYLVETREQIQLVNNELDQRVDQLAQLNLQLYEANRLKSDFLANMSHELRTPLNSIIGFSEVLSGIDSLDDKQRRYATNIQKSGRVLLEMINDILDLAKVEAGKMEVRPVPFDLEMLVRAQADMVRSLSEDKNIQLTVSADDDLPQAKQDQNKFGQILTNLLSNAIKFTPEGGMINVRLALCDEDRFELSVSDTGVGIASEDQKIIFEKFRQSRKVLDGEGLTREFSGTGLGLSIVKELSKLLGGEVSFESQLGRGSTFYVRLPLIFTASPPMPTLHPLLESDES
>NZ_CP036262.1|WP_145353189.1|5141343_5142219_-|NAD(P)H-hydrate-dehydratase
MLNAIERVATLPAPPARNSESHKGSFGHLLLVAGSKTMSGAARLSALSALRGGVGLLTVATAESVWGIVAAENPAWMTLPLAEQDGCCRLQSLSVIESAWERKTALAVGPGLGQTPEVADLVKVCYSRCPLPLVLDADGLNAFVGHVDQLACALEAPRVLTPHPGELARLLGIEVRELQRDRENVAVKFARQTGAVVLLKGAQTVITDGDRLAVNGTGNSGLARGGAGDVLTGLIGALLAQGMEAFSAAQFAAHFHGLAADIVATEKTAQAMLVTELIDAFPAAWKRILAS
>NZ_CP036262.1|WP_145353187.1|5140236_5141310_-|acyl-CoA-dehydrogenase
MSALVLSPQSAALDHLCERLARSANDRQTVSDWPAEALQWCADAGVYRWFLPKSVGGLEWDVEDQTRGFLRLAAADLTTTFVITQAIGACRRIAGSPNSSVAEQWLPRLLQGTAHPTVGISHLTTSRQHLREPVLRAEASGSGFRVSGFSPWVTAAPYADLFVVGATLRSGEQLLAAIPADAEGVKPSPGTSLVALSASCTARVDFDNVFAQGEQVLAGPIENVMQGGTGGMTGGIQTSALAIGLAKAAIEFLSVESERREDLQDIAGRMLEDVQQVEATLLSAAAGNPACDLAELRGEANRLVLRATQAALMSAKGAGYVAGHPVGRWCQEALFFLVWSCPQPVAQSHLCELAGLS
>NZ_CP036262.1|WP_145353185.1|5139363_5139924_+|DJ-1/PfpI-family-protein
MPAPKVLIVIGDASETLDTMYPFYRLQEAGFQPVVIAPEKRLYQMVMHEVKPGWTITKEWEGYTLQADLAFADVDPEAYAGIMFSGGRAPEYIRYDENLVRITKHFFATDKPIASVCHGVEIPAYADCVRGRKMATVPKCKFDLEVCGGEFVDAPCVIDGNLVSGRTFHDNGHYIGPWIELLQAAV
>NZ_CP036262.1|WP_145353183.1|5138577_5139354_+|sirohydrochlorin-chelatase
MSKTGLLLVGHGTRNDQGAEQFQVLTAVLKKQLPHFVVAGCFLELRPPTMEQAWQTLIEAGVTEVAVQPLLLFSAGHAKQDIPDAVDKLATPDIPVRYGRPLSRERNLVTLVCRTAANLLAELSPPQGSVSRTALVMVGRGSFDPCAQADMRLLAETVWRTVNEQLPSGSAGFLSVDTAFYAMAQPRLPEVLREVCSRGNVQDVIVQPHLLFAGQLHYAIEAQVQEVADQFPSKRILVGQPLGPDPLIAASVCNRIQE
>NZ_CP036262.1|WP_145353181.1|5138175_5138574_+|hypothetical-protein
MRFLSYAVAVLVAAGLIYYVGQNPNTDTEAATETTEVAVAAEATTTTDSAELEGQLVTLHVPKMHCPFACYPAVKETLEKTPGVVTVVLAEQKDKNAIDNPEVKIQVSEDFDTEAAIEALASAGFSETTKVQ
>NZ_CP036262.1|WP_145353179.1|5136681_5137722_-|3-deoxy-7-phosphoheptulonate-synthase
MIVILKSGASDQQIDHVIERIEALGLQAHLSRGTFRTIVGVIGDESKVSEDSLRSIPGIAQVIPVLPPYKLASLEAHPQRSVVDVSGVLVGGGNLGMIAGPCSVEEPERMDRLAKSARESGANLFRGGAYKPRTSPYAFQGLGVEGLKILKEAGHRYGLPVVTEVTDPRNVEIVSEYADMLQVGARNMQNFVLLTEVGKSSRPVLLKRGMSATIQDLLMSAEYILSQGNPNVVLCERGIKSFDPSTRNLFDVAAVPVLAGLTHLPVIVDPSHATGRPDLIPACALAGLAAGADGVHIEIHDEPEVAKSDGPQALLPEQYQELAGRMRKMAELLGKTISPPNPEVAA
>NZ_CP036262.1|WP_145353177.1|5135929_5136685_-|triose-phosphate-isomerase
MTRRILIAGNWKMNTRRRDAAALAKGVVDGIPKECAVEIALCPPSVYLGTVSECVVGSPVGLGGQNLYAAADGAFTGEVNAGMLTDIGCSYVILGHSERRQLMGETDADVSKKLHAALAGNLIPIVCVGETQEQRENNETEQVVSDQLKGSLAGLDEARAAGIVIAYEPVWAIGTGLTASPDQAEAVHAFIRGILTDDFGEDVAGQIRLQYGGSVKPGNAAELLGQKNIDGALVGGASLKAEDFLGIINAV
>NZ_CP036262.1|WP_145353198.1|5148515_5150273_-|TIGR03545-family-protein
MIRWRFLIPRILIVVVVIALLRWSIGPIVQYASVQALEASVGARVDIASTTVGLFPPRLEYAGLQIGDPREGKSHTNAFQADLVSFELDGNALLKRRWVARSGRISGLKIGEGRDSSGHLEVPEVIEEPAGPSMLGQWLGGFTDQAVDGLESFGKDLETYQRSEEIRQRWEAEYASLKMRAESLEVEVRAIRDEAKGIDNPLRDLPRLQATIARAEAVRKELIAIRSKLDSLPQQVQVDWLAMEQAKQNDLNRVKEFVPQDFRDTDKIGPDLFKGIVQGQIDRVRSHLDTAREIAGWTITEPIDVERTRGDDIRLVAGPLPPSLLVQQCQIDGDLSINNEVYTMTGILENLTPQTERLTEPLRARMRLEGPRVVRVDFQRYFDEKRPKPRDVLTIHWPNLEVRPHHIGNSDDAQLAIRGGDLDLYVQIEAIGDEMHGKLISRQADTHLALETSAKISELAAVQSLQSRLSSIDRLEVQAEFSGTWSDLDMSLSTNLTGVLSEGMKEAFNVQIADAKQKLNTRIQVEHQQQMAKLQDLLGKQHMATRDILAKADLQIDELKSKLVSELPSASTYLGTLESKLRGLR
>NZ_CP036262.1|WP_145353200.1|5150269_5151127_-|TIGR03546-family-protein
MATASRYGVLERILFCDFGAREAPAMFLWLIKQIFAVKNALAGRRHPHQLAWGLAFGVLLGIIPHGNLLAIGLVVMVLCLNLNHAMTGLAGLAISFFAVKLDPYSHQLGEYVLHHPQMVAPLAQAWQLPFVPWTDLNNTVVMGSLLLGIVALIPVYVLSYFGFSLTVPAVTETPDPTSAEISKNVPAPLAIGKKRDATQTRSEAPVPPSTVPVGMETRIDVIRVADRGAGGQPSGTEKGSQNGRRIDGAHMQVTSPASDADNAQINQALNYLLRRLRQAQQEKTS
>NZ_CP036262.1|WP_145353202.1|5151193_5152081_+|hypothetical-protein
MYTILFLALFPIGIFLAFVVVTVIITLREIHYVWYLAPQESVSDSVSASDTSSRALNARVDIPYQPPAYQQPTLPLTPYAGQKCRDFDSMQYEYLGDFRHAKGGIYKIRYDVWWSKDRYVLALIEAGKVAGIPVSNVSLITLGNPTHKGHPGSSPPQSAKDLPSICITTIVTEAAYEPDLTGATQTMLFPHANSGDQQRFHYQRLKLPSAVPFSANPLEDLYQFRIADAARIFESGNAQHIETSQKMWRPTLRGTMRIVADQYAFMLARRFYSDKRRLRKQLGKLESESSRMSPT
>NZ_CP036262.1|WP_145353204.1|5152143_5153175_+|nucleotide-pyrophosphatase
MPRLQLWGIAPSNEHGTSNTFRLLGLFLVTLASAPFAFAAEPAAANLPQSSKTPKVLLIGIDGLRVDALKKANTPALDQLAAAGSIRYQTRVISEQVPDSDTISGPGWTTYLTGTWADRHGVLDNSFKGRKSDQAPHLFRLTKQGNPDLLTASFLDWTPLNQHVTTDADVNVIVSPNAKMDEYVGGDETIAHMAAALLASRPIDIAFVYLGAVDETGHKHGFHPTVKPYMDQIETTDRHIQRLLEAIAARPTYDQEDWLVVVGSDHGGEGTGHGGGRENSMVYHTAMIVSGDAALPNSKTDETPSVSTTDITAVALTHLGITLEPEWKLAGDATLWLKPSDRQ
>NZ_CP036262.1|WP_145353206.1|5153658_5154801_-|acyltransferase-family-protein
MSAPYRHHDVSVSVKETFQVVALIATVMVVGIHYKSAVPLSAEAADATWNALTQDFLFGGIARVAVPLFAFAAGFFYYRSDDGTWGCYLKKLGQRGRSVGLPYFIVASVAIFAWLMIRRLTNDPANMNWPQFVATWWLHPPAEQLWFLRDLLVLVLIAPVIRFALGASGLRAAVVILILGGAWFLQWEPFPILVGWHFLHIETLFFFALGAVATRYPDWLESICRISTVGVCGLLGLWGVLLLLRINLRADFDLWYSDSYGWLDLFAHKTAILVGGVALFGVAYRLRYPILMRLSGAAFFVYLVHEFPLRAILVRGADQVVPHPYTCWVLTPLVVVGCFVAAVLTTRYFPLAMQTLSGGRVPSVGKRSLPKRSAQANSPA
>NZ_CP036262.1|WP_145355566.1|5155161_5156247_+|DUF1559-domain-containing-protein
MNKRPTRGFTLVELLVVIAIIGVLVGLLLPAVQAAREAARRMQCSNNLKQLGLALHNYHDSHRSFPAAGTLPRGTNVAKYYPGIMVSLFPYIEQGARYDQIQDRLRITSDPWSALFTGSPYDMTLPALLCPSEPNGDSPSPHASNARINYMFNMGDGMLKLDAAWHHPNYISNQYVQAQNRGPFHMDSWKKFASIVDGTSNTLAFSESASASQGYWSREVKGGVGMNSALLEPDGAQPIIHPDVCMTGTIDPNNRRQYLTPTDTWRGNFYQMGTPWNGFHTVVPPNGPSCMDSLTGLYTAIFTPNSYHPSGVNAVYMDGSVRLITDTVDSGDLTQTQPVAGPSPYGVWGAMGTHAGGEVQF
>NZ_CP036262.1|WP_145353208.1|5156333_5156927_-|hypothetical-protein
MKKLLNSFLSGCATMACLMTLGCGELRPDGFPDLYPVTLVVTQDGEPLADAMVSLYPENSSLTRWPVGGMSDASGNVELVTYGKYEGVPAGIFKVMVNKTVHEGDPIPESPAADASPAERAAYDRAIKTGSRESFQVVQKEFRTADKTSLTVTVSPDAENSYTLDVGAAVKEKDQQASAVGGGSADYVPMGESAVAE
>NZ_CP036262.1|WP_145353210.1|5157107_5159225_-|hypothetical-protein
MLPAQSPSRSSWQIAVATGLLWACVIGLTSGCTTTRYISKRHVRENALNTSLNLMRWKGPSLSERTSLQLTRFGLLDQYEKDPKATLEKLQQMAMSQDQELTFAVGELSYVEGVKAERAGIESTALHHYGMAMSNSYQYLFAADLDATRNPYDPQFREACELYNESLEDMLRLLCAENKLRPGQNYTIETPERTFTIDTVARGKWPAAEFERYEFVSDYKVETLHNRHVTYGLGVPLLAVRRPKDGDPHREKYYPDGLSYAVTALLRCTDIDRKPGEPPKHCVLEFFDPLSHNHVELANRWVPLETDLTTPLAYYLDSPQFRERDNATQGLLNPAKSQETRGLYMLEPYDPKRIPVVMVHGLWSSPLTWMDMFNDLRSFPAIRERYQFWFYMYPSGQPFWNSATEMRADLANVRDAFDPMHHDRTMDQMVLVGHSMGGLVSRMQTIDSHQDFWNIVSNQPVQELQGPSETKAKLASALFFKPNQSVQRVVTIATPHRGSDFANDYTRWLARKFIRLPRMAVNTGTLLAARNPGFFKDTKMLTTSNAIDSLAPESPIFPVMMRAQESSEVKLHNIVGLVEKHGLFGRIIEGSDGIVEFDSAHLENADSEIVVNSDHTSVHTKSQTILEVRRILLEHMAELDATDRVADAAGNELAAGGAASYPAAGPIAQLHSPQVADSPNANLPPLLLRHPSIGSTVAQPVVTSP
>NZ_CP036262.1|WP_145353213.1|5159387_5160797_-|Gfo/Idh/MocA-family-oxidoreductase
MRFGILGTGRITRRLVADLQSTAGVQVTAIASRDVDRADWYAQQYGIATGVEGYQALLGRDDVDAVYIALPPSMHCQWAVAAAEHGKHVLCEKPLAISAEEAHRVDAVCQEKQVRWLDATGWLHHPRTANFSGLEQRGKLGTLKHLSSAVSFYEPFQSGDHRLDASLGGGCVLDLGWYAVGLPIWFAGRPLSVYATAVMRHGVPYRMTAMMWFPDDVTATINCGYDVTTRKWFEVAGDSGSIVCDDFTRPWPEREARFWSHDRTGAAESHSFEGNQEQAMLLRFTKPESDLAIYQQQTLDTQQTLEAITQSLQNGQRCDVVFRERETPAFSSVSLVPAKPTVWFLSGDLMFGSRIRAAAEAAGLEFRMSSGLPTGTVGSEASDEPKDAENQTSAENRSLDPVWMILDLSTRGGMLPTLDADSRNRFPHATWLAYGPHVQVSKLKAAREAGIELVLTRSQFDMRLPTLFK
>NZ_CP036262.1|WP_145353214.1|5160816_5162505_-|flagellar-hook-associated-protein-FlgK
MSLFSTINQSAGALRASQMGLQVVGNNIANANTPGYIRQELELIPASATRVGELIIGQGVIPKATRQIIDQALAERMWNASTAAAGADSLQAAYTELEDLVGGLNGGGLEAQLDTFNEALHNLSNAPADPAARELVLEQASALTNMINQTYQEATAGMERANDQLPGVAIELNSLTSRIADLNLEIMVLEGGRALSSDATGLRDERYQLLEEMAKIVDINVQEQASGSVSVFVGGDYLVSEKYAREVYTAYDSDTQGQEIRIVETDSPLQAKGGMVGATTAARDEVWGAYVEELDEFAANLASVFNQVHSQGQGSLGHTSMSGVKNLEPGVPLERAGLQTEPTNGTFDIQVVDANGDLVSTHRINVQKLDIIGDSTINSIVADIDAIDGIQASVDGSGTIQIESESPGMGFTFSDDNSGFLAAAGLNTFFTGTTASTISVNSYLVDNPDQLSVSKSGVGQDTNALADLVDLIKKPQEQFGGLSLQSLQQRSLGSIAQRVSVQRSSADGVSDFYETLRAQHLSITGVNLDEEAIKMITYQRAFQASSRVIATASEMLELLVNL

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Crispr_ID: NZ_CP036262_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_16

5465367-5465804

Orphan

Consensus_repeat	Method
CTCGCCGCCTGACTCGCC	CRT

8 spacers

The CRISPR arrays of NZ_CP036262_16

>merge|NZ_CP036262|16|5465367-5465804|CRT
CTCACCACCTGACTCGCTACCAGGCTCACCACCCGATTCCATACCAGACTCGCCGCCCGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCACCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCACCTGACTCGCTGCCTGACTCGCCACCAGACTCGCC

>NZ_CP036262|16|2|5465367-5465804|CRT
CTCACCACCTGACTCGCT	ACCAGGCTCACCACCCGATTCCATACCAGACTCGCCGCCCGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGACTCGCCGCCTGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGACTCGCCGCCTGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGACTCGCCACCTGA
CTCGCCGCCTGACTCGCC	GCCTGACTCGCCGCCTGA
CTCGCCGCCTGACTCGCC	ACCTGACTCGCTGCCTGA
CTCGCCACCAGACTCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145353602.1\|5474720_5475158_-\|flagellar-biosynthesis-protein-FlgD	unknown	unknown	gnl\|CDD\|235847
NZ_CP036262.1\|WP_145353593.1\|5468735_5469239_-\|carbon-storage-regulator	unknown	unknown	gnl\|CDD\|376847
NZ_CP036262.1\|WP_145353595.1\|5469386_5471264_+\|malto-oligosyltrehalose-trehalohydrolase	unknown	unknown	gnl\|CDD\|200464
NZ_CP036262.1\|WP_145353573.1\|5450693_5451698_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP036262.1\|WP_145353591.1\|5467989_5468568_-\|DUF3365-domain-containing-protein	unknown	unknown	gnl\|CDD\|378734
NZ_CP036262.1\|WP_145353599.1\|5472225_5474667_-\|flagellar-hook-basal-body-complex-protein	unknown	unknown	gnl\|CDD\|235557
NZ_CP036262.1\|WP_145353579.1\|5457154_5458348_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145355649.1\|5478333_5479704_-\|FliI/YscN-family-ATPase	unknown	unknown	gnl\|CDD\|274607
NZ_CP036262.1\|WP_145353571.1\|5449867_5450317_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145353587.1\|5462743_5463547_-\|peptidase	unknown	unknown	gnl\|CDD\|100085
NZ_CP036262.1\|WP_145353583.1\|5460784_5461870_+\|P-loop-NTPase	unknown	unknown	gnl\|CDD\|378455
NZ_CP036262.1\|WP_145353585.1\|5462161_5462476_-\|histidine-biosynthesis-protein-HisIE	unknown	unknown	gnl\|CDD\|237855
NZ_CP036262.1\|WP_145353607.1\|5477615_5478200_-\|flagellar-export-protein-FliJ	unknown	unknown	gnl\|CDD\|131526
NZ_CP036262.1\|WP_145353575.1\|5451697_5454016_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224196
NZ_CP036262.1\|WP_145353581.1\|5459442_5460693_+\|peptidase-T	unknown	unknown	gnl\|CDD\|235484
NZ_CP036262.1\|WP_145353597.1\|5471337_5472237_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381321
NZ_CP036262.1\|WP_145355646.1\|5458376_5459336_-\|3'-5'-exonuclease	unknown	unknown	gnl\|CDD\|99825
NZ_CP036262.1\|WP_145353605.1\|5476977_5477625_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145353603.1\|5475278_5476940_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|350657
NZ_CP036262.1\|WP_145353577.1\|5453990_5456282_-\|sulfate-transporter	unknown	unknown	gnl\|CDD\|223732

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145353602.1\|5474720_5475158_-\|flagellar-biosynthesis-protein-FlgD	gnl\|CDD\|235847	PRK06655, flgD, flagellar hook assembly protein FlgD.	6.41855e-15
NZ_CP036262.1\|WP_145353593.1\|5468735_5469239_-\|carbon-storage-regulator	gnl\|CDD\|376847	pfam02599, CsrA, Global regulator protein family. This is a family of global regulator proteins. This protein is a RNA-binding protein and a global regulator of carbohydrate metabolism genes facilitating mRNA decay. In E. coli CsrA binds the CsrB RNA molecule to form the Csr regulatory system which has a strong negative regulatory effect on glycogen biosynthesis, glyconeogenesis and glycogen catabolism and a positive regulatory effect on glycolysis. In other bacteria such as Erwinia caratovara RmsA has been shown to regulate the production of virulence determinants, such extracellular enzymes. RmsA binds to RmsB regulatory RNA.	6.89735e-10
NZ_CP036262.1\|WP_145353595.1\|5469386_5471264_+\|malto-oligosyltrehalose-trehalohydrolase	gnl\|CDD\|200464	cd11325, AmyAc_GTHase, Alpha amylase catalytic domain found in Glycosyltrehalose trehalohydrolase (also called Maltooligosyl trehalose Trehalohydrolase). Glycosyltrehalose trehalohydrolase (GTHase) was discovered as part of a coupled system for the production of trehalose from soluble starch. In the first half of the reaction, glycosyltrehalose synthase (GTSase), an intramolecular glycosyl transferase, converts the glycosidic bond between the last two glucose residues of amylose from an alpha-1,4 bond to an alpha-1,1 bond, making a non-reducing glycosyl trehaloside. In the second half of the reaction, GTHase cleaves the alpha-1,4 glycosidic bond adjacent to the trehalose moiety to release trehalose and malto-oligosaccharide. Like isoamylase and other glycosidases that recognize branched oligosaccharides, GTHase contains an N-terminal extension and does not have the conserved calcium ion present in other alpha amylase family enzymes. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase. Glycosyltrehalose Trehalohydrolase Maltooligosyltrehalose Trehalohydrolase.	2.13334e-172
NZ_CP036262.1\|WP_145353573.1\|5450693_5451698_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.767e-88
NZ_CP036262.1\|WP_145353591.1\|5467989_5468568_-\|DUF3365-domain-containing-protein	gnl\|CDD\|378734	pfam11845, DUF3365, Protein of unknown function (DUF3365). This family of proteins are functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 198 to 657 amino acids in length.	2.08531e-06
NZ_CP036262.1\|WP_145353599.1\|5472225_5474667_-\|flagellar-hook-basal-body-complex-protein	gnl\|CDD\|235557	PRK05682, flgE, flagellar hook protein FlgE; Validated.	2.02966e-42
NZ_CP036262.1\|WP_145353597.1\|5471337_5472237_+\|aldo/keto-reductase	gnl\|CDD\|381321	cd19095, AKR_PA4992-like, Pseudomona aeruginosa PA4992 and similar proteins. Pseudomona aeruginosa PA4992 is the prototype of this family. It is a putative aldo-keto reductase that catalyzes the reversible reduction of ketones to the respective alcohols using NAD(P)H as a hydride donor.	1.29744e-89
NZ_CP036262.1\|WP_145353587.1\|5462743_5463547_-\|peptidase	gnl\|CDD\|100085	cd06164, S2P-M50_SpoIVFB_CBS, SpoIVFB Site-2 protease (S2P), a zinc metalloprotease (MEROPS family M50B), regulates intramembrane proteolysis (RIP), and is involved in the pro-sigmaK pathway of bacterial spore formation. In this subgroup, SpoIVFB (sporulation protein, stage IV cell wall formation, F locus, promoter-distal B) contains two tandem repeats of the cystathionine beta-synthase (CBS pair) domain. SpoIVFB is one of 4 proteins involved in endospore formation; the others are SpoIVFA (sporulation protein, stage IV cell wall formation, F locus, promoter-proximal A), BofA (bypass-of-forespore A), and SpoIVB (sporulation protein, stage IV cell wall formation, B locus). SpoIVFB is negatively regulated by SpoIVFA and BofA and activated by SpoIVB. It is thought that SpoIVFB, SpoIVFA, and BofA are located in the mother-cell membrane that surrounds the forespore and that SpoIVB is secreted from the forespore into the space between the two where it activates SpoIVFB. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown.	6.93193e-20
NZ_CP036262.1\|WP_145353583.1\|5460784_5461870_+\|P-loop-NTPase	gnl\|CDD\|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	1.51647e-134
NZ_CP036262.1\|WP_145353585.1\|5462161_5462476_-\|histidine-biosynthesis-protein-HisIE	gnl\|CDD\|237855	PRK14900, valS, valyl-tRNA synthetase; Provisional.	4.12905e-11
NZ_CP036262.1\|WP_145353607.1\|5477615_5478200_-\|flagellar-export-protein-FliJ	gnl\|CDD\|131526	TIGR02473, conserved_hypothetical_protein, flagellar export protein FliJ. Members of this family are the FliJ protein found, in nearly every case, in the midst of other flagellar biosynthesis genes in bacgterial genomes. Typically the fliJ gene is found adjacent to the gene for the flagellum-specific ATPase FliI. Sequence scoring in the gray zone between trusted and noise cutoffs include both probable FliJ proteins and components of bacterial type III secretion systems.	1.89051e-09
NZ_CP036262.1\|WP_145353575.1\|5451697_5454016_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224196	COG1277, NosY, ABC-type transport system involved in multi-copper enzyme maturation, permease component [General function prediction only].	1.99963e-08
NZ_CP036262.1\|WP_145353581.1\|5459442_5460693_+\|peptidase-T	gnl\|CDD\|235484	PRK05469, PRK05469, tripeptide aminopeptidase PepT.	0
NZ_CP036262.1\|WP_145355646.1\|5458376_5459336_-\|3'-5'-exonuclease	gnl\|CDD\|99825	cd05782, DNA_polB_like1_exo, Uncharacterized bacterial subgroup of the DEDDy 3'-5' exonuclease domain of family-B DNA polymerases. A subfamily of the 3'-5' exonuclease domain of family-B DNA polymerases. This subfamily is composed of uncharacterized bacterial family-B DNA polymerases. Family-B DNA polymerases contain an N-terminal DEDDy DnaQ-like exonuclease domain in the same polypeptide chain as the polymerase domain, similar to family-A DNA polymerases. This exonuclease domain contains three sequence motifs termed ExoI, ExoII and ExoIII, with a specific YX(3)D pattern at ExoIII. These motifs are involved in metal binding and catalysis. The exonuclease domain of family-B DNA polymerases has a fundamental role in proofreading activity. It contains a beta hairpin structure that plays an important role in active site switching in the event of a nucleotide misincorporation. Family-B DNA polymerases are predominantly involved in DNA replication and DNA repair.	1.59543e-67
NZ_CP036262.1\|WP_145355649.1\|5478333_5479704_-\|FliI/YscN-family-ATPase	gnl\|CDD\|274607	TIGR03496, FliI_clade1, flagellar protein export ATPase FliI. Members of this protein family are the FliI protein of bacterial flagellum systems. This protein acts to drive protein export for flagellar biosynthesis. The most closely related family is the YscN family of bacterial type III secretion systems. This model represents one (of three) segment of the FliI family tree. These have been modeled separately in order to exclude the type III secretion ATPases more effectively. [Cellular processes, Chemotaxis and motility].	0
NZ_CP036262.1\|WP_145353603.1\|5475278_5476940_-\|hypothetical-protein	gnl\|CDD\|350657	cd17470, T3SS_Flik_C, C-terminal domain of flagellar hook-length control protein FliK and similar domains. The flagellar hook-length control protein FliK is a soluble cytoplasmic protein that is secreted during flagellar formation. It controls hook elongation by two successive events: by determining hook length and by stopping the supply of hook protein. It contains an N-terminal domain that determines hook length and a C-terminal domain that is responsible for switching secretion from the hook protein to that of the filament protein, by interacting with FlhB, the switchable secretion gate.	5.58001e-20
NZ_CP036262.1\|WP_145353577.1\|5453990_5456282_-\|sulfate-transporter	gnl\|CDD\|223732	COG0659, SUL1, Sulfate permease and related transporters (MFS superfamily) [Inorganic ion transport and metabolism].	6.21413e-93

>NZ_CP036262.1|WP_145353587.1|5462743_5463547_-|peptidase
MILREPDRSPYDLVFRIGEFPVRIAWTFWLMTAVFGYNFVDYIDYLFLSVYGLWSPSTLPLLLIWSACVLVSITVHELGHALAFRRYGIHSQIVLYHFGGLAIPLAANSPTHSVSRLSAKENLVIAAAGPGAQLLLAAAVILLTRTAGYEVHQAPDFLQSIPGVAGGNPIMDVGLYTLVNSLVWPSVVWALFNLIPVWPLDGGRIAREVIAMLGGNIRHSLGLSIVVGAAMVVVGFMIGQWFMAILFASLLMGNWQEFQRLGQWRSW
>NZ_CP036262.1|WP_145353585.1|5462161_5462476_-|histidine-biosynthesis-protein-HisIE
MAKKKRAAKTAAKKVAKKTAVKRTAAKKTAAKKTAAKKRVAKKRAVKKVVKKAAKRTATKKVAKKKAVKRTATKKVAKKTAKKRAAKKRVSKAAPRKKTATRRK
>NZ_CP036262.1|WP_145353583.1|5460784_5461870_+|P-loop-NTPase
MPDQELTADLVRSLLETFPDPETGRPIGTMGQLGDIQVENKHAKIALGLSTHSYPIANEVKEQIASLVAAKIPGTTVDITVHPHARPPARSGQAGLRIKTVIAVGSGKGGVGKSTVAASLAVTLELLGAKVGLMDADVYGPSIPHLFGLTGKPELTPNKKIVPIKSGDLPVISMGFFVEPDQAVIWRGPMLHQSINQFLGETDWGELDYLVIDMPPGTGDVALTLSQGAVPIAGAVVVCTPQEVALLDAVKAISMFRTVKIPVAGIVENMSGFVCPDCHKRYDIFGSGGARDKAEELSLPFLGELPIDPILRKAGDAGELAAVIRSDARARAPLEKVARALVRNFAQQAALTPPKPSLPTL
>NZ_CP036262.1|WP_145353581.1|5459442_5460693_+|peptidase-T
MSNQINRDRLLERFLAYVGVDTAANPDTTRYPSSAGQWELGNLLTQQLEDLGADYPHQDEHGLVWASVPATDGGNSPTIALIAHLDTSPEAPSANISPQVIKNYEGGDILLPSGQVIRVDQTPELNDLIGSTLITTDGTTLLGGDDKAGVAIIMELAQHLIENPHLEHGTVRILFTCDEEIGRGTDKINLSKLDAAAAYTLDGGGAGDLDVETFSADAATVTFRGHNIHPAIAKGRMVNAVRAAAYFVDLLPRDQQTPETTSGREGFIHAHNIHGGVGNATVELILRSFDTAELDLFADQIRTLAETVQEHFPGLQVDVQVRSQYRNLAEGLQQSPEVVQFAEQAYQNLQRTYRKTIIRGGTDGSQLTEKGLPTPNLSSGQHNIHAVHEFACLDQMEDAIEHLVELLRLWSQQAKS
>NZ_CP036262.1|WP_145355646.1|5458376_5459336_-|3'-5'-exonuclease
MEFLLFDVETIADGQLVAAVKYPTEELEPAEAIERFQEELRETQKGRDFIPHTFQIPIAVVVAKVDSDLNMVDLVSLDEPQFRSHVMTQHFWRGWEHYHHPTWVTFNGRGFDIPVMELAAFRYGLNLKDWFHNKGASYTHPRNRYNANAHLDLHEILTNYGSCWFRGGLDLAATLIGKPGKMATKGDQVQEMWNQGKLQEISDYCRCDVLDTYFVFLRTSVLNGRIDLAREAELVEQTHRWLVERSGECQAYVDYLSCWGDWKNPWEVVEEAATKPVQELPDPTQRGESEVSESGVSDESDVSVGSPVDSLDSDGESSS
>NZ_CP036262.1|WP_145353579.1|5457154_5458348_-|hypothetical-protein
MPNPKSITKRFSTVVIRCLFVGWAIVLTSVAGAQGPPNPPANPAGGFQPLVLNLPVANAAVVQPQQRGRLTTADADQRGLVLEGIAGIPVRMSLPIADPAQFWVITPVNQNLVRIQLSDHGKLWSLTATALAGPVVLQISRRDANQLWRVSGQGAAIRLDSVGFPGQSLAGNTRGVVRLEPTSQVNSQFWLASYQRPPAHLHLPVVRLVQHEYRPLPAGRPARIQLFNSHRSEIRIVLTDLMNQRSYPQQSIQPGQSIPVSLERDLGGEIIERYEVSDSTGRIHVDEFITVVPPAILYDISVYEKFLQSIAIDRTGKSPNVIEDVNYQAKSVGIFPLPAGNALRDGMQIDVWQEAVLQANPGGVRGPISLPSQRTPALSPMEKVLQEQQRLQSRQRP
>NZ_CP036262.1|WP_145353577.1|5453990_5456282_-|sulfate-transporter
MTNETPGETSAVAEDSLQSMLKPANLGKDLIAGVVVALVALPLCLGIALASGADPMSGLIAGIVGGIVVGVLSGSSTSVSGPAAGLVAIVAAQISSLGFEGFLLAVVIGGLLQVALGVAKAGALSAFFPSSVIRGLLAAIGVLLILKQIPHLFGHDSDPEGEMSFWQTDGENTFSSVFYSLVGDIHEGVMVIGFACIAVLVLWEKIPLLKKTQVPGPLVAVVLGIVLNELFKTRSESWVAANEHLVQLPIASSFAEFKGFFVFPDFALLANPAVYLGGVTIAIVASLETLLNLEAVDKIDPKHRNSPPSRELVAQGVGNMVSGFIGGLPITSVIVRGSVNVNAGGNSKLSAIFHGGLLLGSVVLLPGLLNRIPLAALAAILLVTGFKLASPALFKKMWNEGRYQFIPFIVTLVAIVATDLLIGILIGLGVSLLFILNSNLRRPIRRVVESRLGGDVLHVELANQVSFLNRAALDRIFQQAPRDTHILIDASDTDYIDPDVLGMIRDFKGNVAPARGVRVSLRGFRARYGLQDEIQFADYSTRELQDKASAEQVLEMLKEGNRRFVTGQRLNRDFGRQIHATAKGQNPIAAVLSCIDSRVPAELVFDLGVGDIFSVRVAGNVIGSYTLGSIEYGVGVAGVKLVLVMGHTRCGAVTSSVGLLASGQDAKEATGCAHLPVIVDEIIASIDPSELQVLKQSKEEPSEDYVDSIAKKNVLRTVEQIIERSEVIRRGVEEGRVVVAGALYDVNTGRIEFYPLNSLAAQT
>NZ_CP036262.1|WP_145353575.1|5451697_5454016_+|ABC-transporter-permease-subunit
MGPYLSVIADSFRAASSSRILWIALFCVGIFLVALAPLGYRENTVATIGPSEIVRADRLLQRLTDGQQESPSPESSIATALSPEFKARLQQAADTESAPIREEDIAEELNQLIDAETDPWFDEEIWQETTQLKELRDLNAESTSDLTEALKRRRSRLRLEAGLRGEIRPRPEKTISIVYAIWETPIEWPLPKALFHQVLVGSILPVTINGLLGFVGIILGILVTAPMLPEMLQPGSLHLLLSKPISRPLLYLSKFVGGCAFMFLCVGPLLSGVWLILGWRFDLWLPGLFYCIPVYMLLFMVYYSVSCLVALQWKSAIAAALLSIGFWVACGALGLVGVAMEAAVSEPAKIEKVAYFSDDDRDLLISTTKPGLIRSWQSSTAQWQDLPLERYRGEFVYILGPIPIGPDHYALARKSATPMGLSGKGDLTILDISNPELPKARRSIVLPHGTTEIFATTDNGMIAAGPEGLYFATAAAVLDTPTKPPTGGGFMGQLSNLLTPNDETFRSILPRNVYLRSPMAAQMLEDDQMLVYSAGILFRLVRESSDEQPDQWTVAAKRNVEGNASSDTKIAVNQSQVALYRSDEPIRFYDRSDLQLAAELELPSKEKLHSITGNPQAGTFLILQSDQTPLQIKGGAEPSFVSLPKNMVDDSIEYLQYDAAGNLLVAYDIDSLQILPPDGGAVEDLRPNLSNWRRANRYLVQPARYLIPQTGELRAETIRAALQGDTTQTLGEGLFAEKTSQRLDVQRPVFTCLGFTALMLLIGCIKFARQDY
>NZ_CP036262.1|WP_145353573.1|5450693_5451698_+|ATP-binding-cassette-domain-containing-protein
MSASADDPIIEIQDLRKTYRSGLLGGNRLEALQGVSLDVRPGEVFGLLGPNGAGKTTLIKTLLGIVRKTSGQATLFGAPVGTSRSRYRIGYLPENLRVEKHHTARSALQLYGRLSGLSNSVVQQRTDPLLEKVGLQGRDRETVRRFSKGMYQRLGLAQALLHDPDLLILDEPTDGLDPVGRSEMRNLLRQLRDEGKTIFLNSHILQEVEAVCDRVAVMAKGTLRGVGSIAELTANREFIEYQVHVAGPVDATLAAIPDSLRKNASAVPLLLQDGSDGCELKLNCDIEAAGAGDLDAAVDGLRKHGLSIRHVQRAKQSLESAFFALVDDTSEEVR
>NZ_CP036262.1|WP_145353571.1|5449867_5450317_+|hypothetical-protein
MGQETSTQRFSKRTLRQVSLDSVRALTGAFYCPDRSTVESFHCIDFQPETETSFGRQLWYFDAIATNEHNRELVVYGFLEYSEEFGSMEIVQDGVFESIAQRARFETVYHTATLKPTWRHPSHRWLFIGMTLVGSIWLASLLLNKLLAS
>NZ_CP036262.1|WP_145353591.1|5467989_5468568_-|DUF3365-domain-containing-protein
MNTSFRSIGLFLIVASALVNQAVAEPPTKTETPSAATVAAVLPAPNLSEVEQRSRILHELISGSLQVMHRDLFDEDESLAIPSHSLEDVFSEMEESFQIEIRWMSVNTDALNTDHLPSDAFERQAAKVLASGKPHFAEAEAGRYRFAGPIRLASQCLKCHVQRRTSNEDRLAGLLISMPFEETPPAEKTESK
>NZ_CP036262.1|WP_145353593.1|5468735_5469239_-|carbon-storage-regulator
MLVLTRKTQEAFELPDVDVLVRVLRCSPSNVQIGIQAPLAIRILRSELHHNDLRTLPGESGQSQQQASRLIRRLESQLAALDGLAGGVELSAVDGAHLTSLVLEEAHETLRQLRRQLVVSQCRDIPSLETRSQGQVKAVTGSVATSVPENVASDRVRQSNSVYAVSA
>NZ_CP036262.1|WP_145353595.1|5469386_5471264_+|malto-oligosyltrehalose-trehalohydrolase
MGNRSPTPHRKRNVTINFDSPATPLKNAFGPRFLEDGTVQFRVWAPACDSLHLRLSQNGTLLRLPMERQADGFFESKAAAQSGELYSFELPNGQHRPDPASRFQPEGVHGPSQLVDDRQYQWECQSFAGTATANLVIYELHIGTFTKAGTYEGAIGRLDELVALGINAIELMPLAQAAGRRNWGYDGVNLFAPNHHYGTADQLRQLVDAAHQRGLSVIHDVIYNHFGAEGNYLHEFGGYISKHHKTPWGDAPNFDEAPCRPARDWILANAIYWLESFQMDGLRLDALHCMGDTSSPHIVTEIGQTFADLRSTATRPYHLIAESNIYDEELIKEVSKSGDTGHGFDAIWCDDFLHSVSAIVRPGEHMSCRQYDPKDDLHTLLQRGYLFAGSLHAEPQRVPPEADPQSVALEKLVVSIQNHDFIGNHPAGLRFHQHSSLELHRAAAALMLTYPAIPMLFMGEEFATDSPFYFFSDFNDGHLRTAVEEGRRREYPQHDWSNSPSPLSVAAVNKSRIGPASEGDLQTRLWYRQLIQLRQSWQTQNLLTSANLKANWSAEDSLAKMTYQLGEQEAVVMVRLHPADANIKDLTVAFDGEVLLKQNGSAVSGHAGQWNLEPAGVLIGIQAAR
>NZ_CP036262.1|WP_145353597.1|5471337_5472237_+|aldo/keto-reductase
MLPKRMLGNTGMEVTQLGYGTMGLRGPKTWGVRVVDEADAEVFLNLVLDSGINFIDTAPDYGIAEERIGRYLSDRRSEFYLATKCGCVFTQHGDHLEIDHEWDTDVIRRNIDTSLARLQTDYIDLLQFHGGDAQTLQSTGLIRLLEEYRDQGVIRHLGISSKLPNLEGLIDLKVFETFQIPYSCLTPEHGPAIARAAATGAGIIIRGGIAHGGPDAEIKREPLNDLWTAANLDALKPDEMTRAELVLRYTLSNPHCDTTIVGTCNKDHLKANLAAAKAGPLPDTLVQAISQQVASVLST
>NZ_CP036262.1|WP_145353599.1|5472225_5474667_-|flagellar-hook-basal-body-complex-protein
MGLASALTTALTGLSAAETQIDVIGNNLANSQTVGFKESRVNYATQFLQTLSLGAAPTVDNGGTNPRQVGLGVQVAEIAQNFAQGTIEISSSPSDLAIQGDGFFMVEAASGERLYTRNGIFKLNADGELVNSTGQRLLGYGVDDLFRIQQSGLVPLEVPLGTESVAKATENVTLEGTLTPEGDVATVSQVIESQVLGDGMVPRPDGTSVALSTAPLPSSSGVSVDTTAAGTVPAGTYEYRVALVDSTGNESVLSGSIAATVGAGNSIRLNGLPVDADGRDYPTVNVYRTDTNGSDLFFLGSAASGGDFIDDGSAAIDLARPADTENLTGNYSYMVTYYKAGEPESRPSPILGPRNVANGRITLTDFPDPPVPPESGGFPEYDSIRIYRNLAGDQNNFFLVDTVSPGETYTDSKTDAEITDLTVSGNKTLDRDGPTIDSNTLLTNVLRRDGATYEAIFKAGTLSYEGRKGGRALGAKELTITENTTVQELIDFVEAASGVQTSQIDAQNPIPTSENNITGESGELVPGGLIKDGAIRFVSNTGELNALEIDLTAFRLTDELGNVTVPNMAFGTVQEAEGQSAASDFIVYDSLGVPINVRVTAALESRSDEQTTYRWYADSASNQVNDSNAITVGTGLVTFDGNGNFVSSTNSRVNVNRQGVPSVSPLQFDLDFSAVSGLASQDASLAATRQDGSAPGVLNNFVVGEDGGLRGVFSNGITRDLGQIRLARFANPVGLEVRGANLYAQGINTGLPVEGAPGENGIGTVVGGALELSNTDIGKDLVGLVLASTQYRGNSRVITTSQQLLDELLNLRR
>NZ_CP036262.1|WP_145353602.1|5474720_5475158_-|flagellar-biosynthesis-protein-FlgD
MSAINTSGSSVQSAENLSSSNQNDGFSDVNMDQFLQLLITEMQNQDPMDPMENSEMLQQIGQIREIGATDQLTNTLAGFAQNQELITASGLIGQQVDALADDSTEVSGVVDKVTIETGEDDSRNVKVHVGGKTIDIKNIRQINSA
>NZ_CP036262.1|WP_145353603.1|5475278_5476940_-|hypothetical-protein
MNTSNSLDHQQALSLRGPSAFSTRSLQAISSGSGQSSVGDGFAELFQVVASATSVTANSASSSLAPSSDSVEASEEASDVDDEEQDSVAVRPSADSASQNETPVVGIAAAANTANDQEAEQEPEEDADVGAAEELTDESNDSEDPTTKEAAVDAEMLLVPEGEASPERASESSAEVPGEETLVSATLGKETDSKASIEGPITGDQTAELAATADSEVTDESGKVAPSAESTDGESPAGFAGKVEVDPDGGSDRRRQGGREKGKRGLEKTPADARAIEGSPQPSGSPDEVSAAAQSSGKPIPSGLLNGAIPVDAAGDLEVQAPPPVVAATPIASAQVAAAGAALQATTNGRKDASGKTSLVKSSGAETEAIQNTNATSDRLNTATKGTAGAKQADGPRVADRALLVQRVSKAFQRLGVDGGQIRIRLHPQELGGVQLQLSMQGSRMNAQVVAETELARSLINEHLPELKQRLADQGIQVERFDVRLDGEQTAAQNRDFAEQQSSSEQRQASGKSAASQSRNLSSGQPAVDGPPPPKAVRSVIDAAKFKSVDLVG
>NZ_CP036262.1|WP_145353605.1|5476977_5477625_-|hypothetical-protein
MGLVIRLFAGICIATIVTQGIVLGVCAGRGTLNAGSITQIVALLNGIDITGDRLRMIVEQSESTERPTYDQILMARTREGLDMDLRLDSQKRYSKELEDKFAELKRDQKLFDERREEFFAKLDEVRKGVMDDGMQELTETLQALDTEQAKIQLVRMIEDNRIEDVVSIIQATPIDKRSDILAEFVSQPEEEMLADILRMIGDGEPAKSLIDRSGK
>NZ_CP036262.1|WP_145353607.1|5477615_5478200_-|flagellar-export-protein-FliJ
MPESLRSATFILQWRILSMARFAFRFEALLRLRENERDAVRGHVADAIQAQSILEQQRDALQQQREESRLQAQRRLASTQLSVDTLLHEGRFDLQLAAEIQGLDTNIRIVQTEIDRRQETLQVADVEVKRLERLREQQYQQWTAAQLAAEQTELDEIAQLRFARAAASQQKLGRVRGRSGADTEPEDKGARAWD
>NZ_CP036262.1|WP_145355649.1|5478333_5479704_-|FliI/YscN-family-ATPase
MCDAVCESTLIQIRGRVAAVSGGNIEIEGMTAPVGAVCRIRMAGNQTCLARLIGFQGVRPILAPLAFPDGVAAGDEVELLATRARIHVGPELRGRVINALGEPIDGRPLPAGLQPAELERDCPDSLKRPAISKPLETGVRAIDAFLTCGLGQRIGIFAGSGVGKSTLLSMLVQGTAADTIVVGMVGERGREVREFIEHSLGPDGMKRTIMVAATSDQPAALRVQAAWTATAVAESLRDAGQNVLLLIDSVTRFALAQREIGLAAGEPPTTRGYPPSVFAMLPRLVERAGTTEQGSITAFYSVLVEGDDTNEPIADTLRGLLDGHVVLSRELASQSHWPAIDILASLSRLQTRVVSPEVREAAEILRRSMAEYKRNEDLINIGAYKAGSNPHLDQAIAIREPLKQLICQATLEAKSGQTDRLTQTHLEMVRLANALKGVNAALQQGAETPQPNGGTP

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Crispr_ID: NZ_CP036262_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_17

5983566-5983728

Orphan

Consensus_repeat	Method
CCACTTTCGTAACGGATCGGCGAAAGTCGAATCGTCGTAGCGTGGGAGAACC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_17

>merge|NZ_CP036262|17|5983566-5983728|CRISPRCasFinder
CCACTTTCGTAACGGATCGGCGAAAGTCGAATCGTCGTAGCGTGGGAGAACCAAGCTGCTGGCCGGTCGGCTTGCGCCGATCCGCTAAGAATTCCAACCGCAAATCGCCACCCACTTTCGTAACGGATCGGCGAAAGTCGAATCGTCGTAGCGTTGGAGAACC

>NZ_CP036262|17|13|5983566-5983728|CRISPRCasFinder
CCACTTTCGTAACGGATCGGCGAAAGTCGAATCGTCGTAGCGTGGGAGAACC	AAGCTGCTGGCCGGTCGGCTTGCGCCGATCCGCTAAGAATTCCAACCGCAAATCGCCAC
CCACTTTCGTAACGGATCGGCGAAAGTCGAATCGTCGTAGCGTTGGAGAACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354078.1\|5996553_5996949_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366443
NZ_CP036262.1\|WP_145354073.1\|5986421_5987795_-\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP036262.1\|WP_145354079.1\|5997437_6001253_-\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377876
NZ_CP036262.1\|WP_145354065.1\|5967124_5969557_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275327
NZ_CP036262.1\|WP_145354072.1\|5985090_5986281_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	unknown	unknown	gnl\|CDD\|335469
NZ_CP036262.1\|WP_145354076.1\|5992523_5994818_+\|ribonuclease-R	unknown	unknown	gnl\|CDD\|273947
NZ_CP036262.1\|WP_145354063.1\|5962542_5964468_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379232
NZ_CP036262.1\|WP_145354074.1\|5988097_5989519_-\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|273938
NZ_CP036262.1\|WP_145354070.1\|5981133_5983491_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145355762.1\|5969775_5969952_+\|transposase	unknown	unknown	gnl\|CDD\|372671
NZ_CP036262.1\|WP_145354075.1\|5989939_5992426_+\|glucuronate-isomerase	unknown	unknown	gnl\|CDD\|235087
NZ_CP036262.1\|WP_145354077.1\|5995378_5996323_+\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036262.1\|WP_145354068.1\|5977079_5979425_-\|polysaccharide-biosynthesis-tyrosine-autokinase	unknown	unknown	gnl\|CDD\|349772
NZ_CP036262.1\|WP_145354071.1\|5983898_5984903_-\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|237845
NZ_CP036262.1\|WP_145354062.1\|5960616_5962536_+\|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl\|CDD\|132152
NZ_CP036262.1\|WP_145354066.1\|5970363_5974389_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275327
NZ_CP036262.1\|WP_145354069.1\|5979446_5980520_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224512
NZ_CP036262.1\|WP_145354064.1\|5964590_5966951_-\|TIGR03032-family-protein	unknown	unknown	gnl\|CDD\|379811
NZ_CP036262.1\|WP_145354080.1\|6001212_6001971_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225731
NZ_CP036262.1\|WP_145354067.1\|5974528_5977036_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273357

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354078.1\|5996553_5996949_+\|hypothetical-protein	gnl\|CDD\|366443	pfam01060, TTR-52, Transthyretin-like family. TTR-52 was called family 2 in, and has weak similarity to transthyretin (formerly called pre-albumin) which transports thyroid hormones. The specific function of this protein is as a bridging molecule in apoptosis cross-linking dying cells to phagocytes. TTR-52 bridges by cross-linking surface-exposed phosphatidylserine (PtdSer) on apoptotic cells to the CED-1 receptor, a transmembrane receptor, on phagocytes. TTR-52 has an open beta-barrel-like structure.	0.000809107
NZ_CP036262.1\|WP_145354073.1\|5986421_5987795_-\|O-antigen-ligase-family-protein	gnl\|CDD\|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	2.40532e-08
NZ_CP036262.1\|WP_145354079.1\|5997437_6001253_-\|DUF1553-domain-containing-protein	gnl\|CDD\|377876	pfam07587, PSD1, Protein of unknown function (DUF1553). A family of proteins found in Rhodopirellula baltica.	9.44058e-41
NZ_CP036262.1\|WP_145354065.1\|5967124_5969557_+\|hypothetical-protein	gnl\|CDD\|275327	TIGR04534, hypothetical_protein, ELWxxDGT repeat. This model describes protein repeat with a well-conserved motif ELWxxDGT, and a periodicity of about 48. A single protein may have as many as 18 repeats. It may consist nearly entirely of this repeat, or may have other repeats as well (e.g. hyalin repeat). It is most common in the Deltaproteobacteria.	1.50964e-19
NZ_CP036262.1\|WP_145354072.1\|5985090_5986281_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	gnl\|CDD\|335469	pfam03781, FGE-sulfatase, Sulfatase-modifying factor enzyme 1. This domain is found in eukaryotic proteins required for post-translational sulfatase modification (SUMF1). These proteins are associated with the rare disorder multiple sulfatase deficiency (MSD). The protein product of the SUMF1 gene is FGE, formylglycine (FGly),-generating enzyme, which is a sulfatase. Sulfatases are enzymes essential for degradation and remodelling of sulfate esters, and formylglycine (FGly), the key catalytic in the active site, is unique to sulfatases. FGE is localized to the endoplasmic reticulum (ER) and interacts with and modifies the unfolded form of newly synthesized sulfatases. FGE is a single-domain monomer with a surprising paucity of secondary structure that adopts a unique fold which is stabilized by two Ca2+ ions. The effect of all mutations found in MSD patients is explained by the FGE structure, providing a molecular basis for MSD. A redox-active disulfide bond is present in the active site of FGE. An oxidized cysteine residue, possibly cysteine sulfenic acid, has been detected that may allow formulation of a structure-based mechanism for FGly formation from cysteine residues in all sulfatases. In Mycobacteria and Treponema denticola this enzyme functions as an iron(II)-dependent oxidoreductase.	4.17289e-38
NZ_CP036262.1\|WP_145354076.1\|5992523_5994818_+\|ribonuclease-R	gnl\|CDD\|273947	TIGR02063, Ribonuclease_R, ribonuclease R. This family consists of an exoribonuclease, ribonuclease R, also called VacB. It is one of the eight exoribonucleases reported in E. coli and is broadly distributed throughout the bacteria. In E. coli, double mutants of this protein and polynucleotide phosphorylase are not viable. Scoring between trusted and noise cutoffs to the model are shorter, divergent forms from the Chlamydiae, and divergent forms from the Campylobacterales (including Helicobacter pylori) and Leptospira interrogans. [Transcription, Degradation of RNA].	0
NZ_CP036262.1\|WP_145354063.1\|5962542_5964468_-\|hypothetical-protein	gnl\|CDD\|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	2.03781e-06
NZ_CP036262.1\|WP_145354074.1\|5988097_5989519_-\|trypsin-like-serine-protease	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	8.10866e-104
NZ_CP036262.1\|WP_145355762.1\|5969775_5969952_+\|transposase	gnl\|CDD\|372671	pfam13683, rve_3, Integrase core domain.	1.2649e-06
NZ_CP036262.1\|WP_145354075.1\|5989939_5992426_+\|glucuronate-isomerase	gnl\|CDD\|235087	PRK02925, PRK02925, glucuronate isomerase; Reviewed.	1.38316e-21
NZ_CP036262.1\|WP_145354077.1\|5995378_5996323_+\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	4.00789e-51
NZ_CP036262.1\|WP_145354068.1\|5977079_5979425_-\|polysaccharide-biosynthesis-tyrosine-autokinase	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	1.37817e-57
NZ_CP036262.1\|WP_145354071.1\|5983898_5984903_-\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	2.36592e-173
NZ_CP036262.1\|WP_145354062.1\|5960616_5962536_+\|asparagine-synthase-(glutamine-hydrolyzing)	gnl\|CDD\|132152	TIGR03108, eps_aminotran_1, exosortase A system-associated amidotransferase 1. The predicted protein-sorting transpeptidase that we call exosortase (see TIGR02602) has distinct subclasses that associated with different types of exopolysaccharide production loci. This model represents a distinct clade among a set of amidotransferases largely annotated (not necessarily accurately) as glutatime-hydrolyzing asparagine synthases. Members of this clade are essentially restricted to the characteristic exopolysaccharide (EPS) regions that contain the exosortase 1 genome (xrtA), in genomes that also have numbers of PEP-CTERM domain (TIGR02595) proteins.	7.90065e-151
NZ_CP036262.1\|WP_145354066.1\|5970363_5974389_+\|hypothetical-protein	gnl\|CDD\|275327	TIGR04534, hypothetical_protein, ELWxxDGT repeat. This model describes protein repeat with a well-conserved motif ELWxxDGT, and a periodicity of about 48. A single protein may have as many as 18 repeats. It may consist nearly entirely of this repeat, or may have other repeats as well (e.g. hyalin repeat). It is most common in the Deltaproteobacteria.	2.8229e-18
NZ_CP036262.1\|WP_145354069.1\|5979446_5980520_-\|hypothetical-protein	gnl\|CDD\|224512	COG1596, Wza, Periplasmic protein involved in polysaccharide export, contains SLBB domain of b-grasp fold [Cell wall/membrane/envelope biogenesis].	1.60493e-17
NZ_CP036262.1\|WP_145354064.1\|5964590_5966951_-\|TIGR03032-family-protein	gnl\|CDD\|379811	pfam16261, DUF4915, Domain of unknown function (DUF4915). This family consists of uncharacterized proteins around 370 residues in length and is mainly found in various species, such as Shewanella, Rheinheimera, Saccharophagus, Leptolyngbya and so on. It contains serveral TPR repeat-containing proteins. The function of this family is unknown.	2.94532e-141
NZ_CP036262.1\|WP_145354080.1\|6001212_6001971_-\|hypothetical-protein	gnl\|CDD\|225731	COG3190, FliO, Flagellar biogenesis protein [Cell motility and secretion].	3.70364e-15
NZ_CP036262.1\|WP_145354067.1\|5974528_5977036_-\|hypothetical-protein	gnl\|CDD\|273357	TIGR00947, 2A73, putative bicarbonate transporter, IctB family. This family of proteins is suggested to transport inorganic carbon (HCO3-), based on the phenotype of a mutant of IctB in Synechococcus sp. strain PCC 7942. Bicarbonate uptake is used by many photosynthetic organisms including cyanobacteria. These organisms are able to concentrate CO2/HCO3- against a greater than ten-fold concentration gradient. Cyanobacteria may have several such carriers operating with different efficiencies. Note that homology to various O-antigen ligases, with possible implications for mutant cell envelope structure, might allow alternatives to the interpretation of IctB as a bicarbonate transport protein. [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	1.00814e-10

>NZ_CP036262.1|WP_145354070.1|5981133_5983491_-|hypothetical-protein
MPLFLLAFFCCCAASQVVNAQKTIPEDPWARFHFEGNQAFSDAALRKALIADPTFLLATHPLGSSDELEGVIRNGLVYGYRRKGFPSPIISVTSQADPPLTTIRIDEGARMLCGKIRIQGGVTLDPERLIERLTKRFPKPNTFPAFVEAGGEIRQRWVNEKGKTVPLVDPVWEPGTPVSLDTETELHAAVVRGIADLGYSSAIVFTRVELNEETHSASLVIEIAEEGSKDKAESIECIGYQVNTPEQIAQAIGWHPNDEIDRSKIEEWTKQLWLSGRFSDQSVRFLRNKEGSGYLVVKVTEVPKMPSLGQSLSESAEVFRRAGNWIGGSQERHDDLVFTFVDDHRRLRWIQSSKGSLLQYFSSSEPNESIPRWSILFDDEQLVLDHQANPLHWSAGIAGADFHVHAQTGILADGKSEDGFARLNFTGNWKTGRNEGQSLFQHAFAVSPADWLAFAYKPGLEQKIVDGVLIAEHPKQRCRIDVATGRVLQWDSDRGGVYFQKGLYEKERTVLLDAVAEKQNAYQAKHPLTSLAQFLCAAPIWNDIHEAIRDGEPVVEEASDAQRRAVQKLLAAGLLEPLDLWIGKQEQGRGEERFFVPSNDLGPKSPFGMGIQLVARASLEYGPQIFPEGEWPLKVLRESALVGLGKPRYFKPVLKGLLEDPKIGPLCLGSVAGLLAHIDSNLASQLARQALLRVDQEHFASDLTGLLAGPGGNWFKEMLSALEGLEEEEWDALSSGVLKNFPRGQALLQRIREQLIKQDSHIDKAIYQVIEPDLRSALQGMVKPT
>NZ_CP036262.1|WP_145354069.1|5979446_5980520_-|hypothetical-protein
MRRIKCCCLVALLFAALGCSHARYSVANLPPEFHAPHHISARHVDLSKMTRNSVPTEWLQPGDTIEVSIVTGVEEGATPKWNLLVDNNGTIDVPLVGPAKVSGLTPTMAADRIRDTSIQKGIYIDPKVMVSIEEKRTFQISVVGAVNEPATYEIPASNCDLLTAITMAKGVSDEASRYIEIKHSPTTLSDLAKTAPVTGPDGVALASFQSGTPPAMVNLDLGQLESQPPGALQLYDGSVVNVMREPKRMVSVIGLVTKPGQIDMPDGEDLMLMDAIAQAGGTTLSIADKVHVIRTLPGQAAPAVIEASISDAMSGGPDNMRLAQGDIIRVEETPSTIALQTIRSFFRVGFSAAVPGI
>NZ_CP036262.1|WP_145354068.1|5977079_5979425_-|polysaccharide-biosynthesis-tyrosine-autokinase
MNQIENLSGPQHLTAADAIQALLRFGNGMMRRQRMVASVFLLVGLFAGIYYVTADRVYQASAQLLVEEPSIGVFPGASPTAQSNKLPTQEKIIRSDRVLKQALDQLRQMDSSLQIDLVGLSDEQALTTLQGNLTVQLVRNTNVIELSYRSASPKAAEVVLDVLVQSYLDFMQQHHQDTSVTVLELLKGEREKIEETLHLEQQRLIKLRDEAHVVGFDNDSLKSHPALQRVNSLNESLTQAQKTRIELQAISAVVSDAIREGRDPRPHMHAVDPDAARSLTAAVLGVAPEQMRSIHVLEQKLLSDRAEVMRLEKHLGPTHPSMVALQGEISNAETYLSDFQARVNGRSSNQSGGQFAALLGDLVQQKLNESTQHEALLRKEYDTLEKEVVAMNGSLSEMLLSQREVDRLSRAYDALLEKIHGVDLGQDQAAVRVAVIGKPKALIAAVSPRLRLVVLAAGFFSTLLSVGLVYIADLRDDRFASLEEAERQTRTEILAVVEKLETYGEYGAEAIQMHVAPSTRSSEAFRTLRAGLMLNPAKPRLIAVSSSEPGDGKTTISSNLAVGLAQAGKRTLVIDADLRKPGMTNLFNVRHAKGLSQLLVEMSPVDVVDKYVMSTGIDNLELIPCGARPLDPAELLASNALSDIVQWAASRYDHVVLDCPPVLIANDVALVTRLTDGLVLVVRPEKNSRRHVLRAIERLERFQTNVLGMVINAMDASTADGAYGYGYGYGYGYGDELTDEKQAVVMPSQNAVSQSELVVHTDSAAPKTAPVRRSTPRRRAA
>NZ_CP036262.1|WP_145354067.1|5974528_5977036_-|hypothetical-protein
MPQSIEPQIESELPSVLFNAGSQGRWVRVAHWLMDASLLVVLFAAPLVLGGRHPLGRLVLIAAVVPGTVGMLIKVIAGRKIPLTWLQISLLLGCLLVPVCQVAVFSPEFIGRFAPGIEHLFGEDPVLVSQGVVTTTFSMSQVTTVKSIPTLLAYLCFFSFLVCRLDDFSDVERLLRWFIGSVLLLTVLAILQSQFGNGRFLWWYDHPSREPGDIPRGPFQNENHLASLLALAVPCSLYFLFRNIKSKSSKLGARISFEQCLAAVTCLVIVVTVFATPSRGGAAIIVFGGVVWGALLGWNLLSKRLAGIWMGYAGWMRTGVVAGWAAAVTGVFVMFNGIERFSYWRYKIWAADIAVWRDFPLLGIGVGNHRYAYRAYLDEYWYQTFTTAESSWLQLLVETGAVGVTLAVLIVIAVLVAALRIVASYSRGVPFLLGSAILAGLAVSCFHASGDFPWHIPSCFVGCMVLVVAAVRLPAVLVDRFGKPSQVLVPMPTKGVGGVAAIGIAVALLVGNYWAITKAIPDARASLQWDAYRRLVRDQPDLNQATGDNQATRLLLATLKADPSHIAARSKLVFRMSAELEQSRFEHADISRLAKQVLNQSSLVVGFCPLESRSYLCAAIAASALGANVEQQERLLAQSQRLRPVDGAVALRRGLNAVMVQEMERADVHFKIALNDDPSMRDRAVETLTLLLSPKEIVERCQPGQEATAMLYQRTRKPVPDEMQQFLGRYYCACLETAAAACENEADAEQFRAAAAKVATEINDSALQLEIAGKRLRSNDRNIALLLTRAEIYLDMGQYEDAQADLRRCQKEAPQNPDVRRFALRLDRQSATLHR
>NZ_CP036262.1|WP_145354066.1|5970363_5974389_+|hypothetical-protein
MSLSCRRPTFSSDRDASSFCHLRPSGFQISLHDPITGFGICKDTPFHGIIKRPGRALLFLNNWLPRLRVYPIQKTLFDVDSLMKRSKRRTLSLTRRRTLDVQPLESRWMLAANPVMLSLGADGGSFFTELHDTVYFAANNDELWKTDGTLAGTEMVYDLRESDDPGLGTFLISEIKVFDEQLAIATYSINDSLELWVSDGSHEGTRFVHEFDNPQNSSEGLTFTEAGGQLFFAASDPVNGLGIELWKTDLTTGGTTMVADLNQSEPGSYTPTYLTNFNEELFFAAGDPGEDESDGWELWKSDGTEAGTTMVTDVNGPGGFIWKPTVSNGEIYFGAWDDDVNGDFSTQLWKSDGTASGTSLVTDFGINALGFFDGIEVNGKLIGIVVDPVSGPELWTTDGTSAGTGIVKDIFPGETGSFPGSLTKFNNELYFTADDGTHGKELWKTDGTEAGTVLVADIESGESGSSPYGFGYPSQFGHDNDRLYFSAYSATNGYELWSTDGTSLGTQMVADLAPGTSESPPGNVIQNSSYFSGLAFVNDHIFFSTYETDTSESGTYVLKPSNLVTLLPDATANLLTEMNGMGYFVINQNELWKTDGTVTGTQLVHDLSNLSNFQITEIEVVNNQLAMTAAIYTGGNSIELWASDGTSGGTNRIFDFGDSPSNSRGLSLTEVGGQLFFTPIDPVSQTGIELWKSDLTTGGTMMVAEFDQAETAGYSPGYMTSFNGELYFTAGDPGAPGDGESDGWELWKSDGTEAGTTMITDVNGPDEFINRPTFFNGEIYFGAGKSDFSYIYFSRLWKSDGTKTGTSLVKDFGENSSAFFNGPELNGKLIGFVSNATSGAELWATDGTPSGTGMIKDIFPGELGSQPYYVTKFNNDIYFSADDGIHGRELWKSDGTESGTVLVADINPSDEESSADGFRPLNQFIEWNNRLYFNAYTRPNGEELWSTDGTSQGTQIVADVIPGPDAPYLRETALVRGRLVFAGYSGTYVLNPSNVDSIFAVSSNDTVIRAQRADSPGSLVTTSVLSLPPNLEGRDVLTADTNGDGKSDLLVRAADGWWYVSESAPNGGWTPFVKHVYWSTSYAWDEVRTGDFNGDGLEDLAGFEATGGRWLVSSSQATGLASSSIQTIWSPTITWSDIQVGDFNNDGRDDLFARAGGNKIVVAKSTGTNLPTTTWVTLAATEEWKDVLVGDFDGDGNDDFTARANAGGSIITGLSTGTAFSVSAWAHWSAAVDWSNTRVGDFNNDGRDDLITLGAGNRWMVVGSSGTAFDSQVTASWAASLSFHEVLVLDLDGDGNDDLATRTANNQWYVWTAPLQSINLRNWGTWSANVGWRSIQTGTSI
>NZ_CP036262.1|WP_145355762.1|5969775_5969952_+|transposase
MATIGVETLYLKPGEPGQSGVCKSFNGWLRDEYLSQTDLMNEDDAPNKITNLACGLQH
>NZ_CP036262.1|WP_145354065.1|5967124_5969557_+|hypothetical-protein
MKRLKKKSQPLTRRRSLSVQTLETRQMLAANPILQLPGLAHGGMFTDLNDTVYFAANDGELWKTDGSVAGSQLVHDLGSAEESVRITITEMSVFNDQLVLTASDESGTVDLWVSDGTNGGTQQVYEFGGAAFSSDGVYFTEAGGQLFFSVKGLAPDSEYEIWKTDLTSGGTTMVTDLSTPGPYSESPRNLTSFNGELYFTAIDPGDSETDGRELWKSNGTVNTLVTDVNGPDGQLVGPVIANGELYFGTRSTDGSGISSSQLWKTDGTIGGEILIKDFGNDAPGLERAVEFNGKLIGVVTDEASGTELWVSDGTSAGTGLLKDIVPGDTGSYPTNLTKFNNELYFSANDGIHGAELWKTDGTEAGTVLVADINPGPDGSYPYGTGYPGVFAEGNNRLYFSATTATNGSELWSSDGTSQGTELVADLVPGTDGSYPYSMTFLQDHLFFGTYGINDGTFVLNPSNVDSIFAVSSGDTVIKAQQGASPGSLSSTAAIALPGNLAGRDVLTADTNGDGISDLLSRAADGWWYVSESAPNGDWTPFVKHVYWSTSYAWDEVRTGDFNGDGLEDLAGFEATGGRWLVSSSQATGLASSSIQTIWSPTITWSDIQVGDFNNDGRDDLFARAGGNKIVVAKSTGTNLPTTTWVTLAATEEWKDVLVGDFDGDGNDDFTARANAGGSIITGLSTGTAFSVSTWAHWSAAVDWSNTRVGDFNNDGRDDLITLGAGNRWMVVGSSGTAFGSQVTASWAASLSFHEVLVLDLDGDGNDDLATRTANNQWYVWTAPLQSINLRNWGTWSANVSWRSIQTGTST
>NZ_CP036262.1|WP_145354064.1|5964590_5966951_-|TIGR03032-family-protein
MTELKPTREVRFEFTNELPGLLNDLGISLLATTYQAGKLVAIGTQRGQLEMQMCSVARPMGLAVSAGCLAIGAQEAVWFADACPEMARQIEPAGRFDAGYSVQRASMTGDIAIHDMAWGNDDQLWAVNTRFSCLCLCDDQHHFSPVWKPPFISNLAAEDRCHLNGLAMQNGKPRYVTVMSQTDTAEGWRPSKATSGCILSVPDGRCLVSGLSMPHSPRVFQNRLFALNSGLGAIGWYEKGQFQTLSKQPGFTRGLDFYGHYAFVGLSKIRETSTFGGIPIADDRDSLKCAIVVVDLRTGKRVAHFEFLAGVDELFDVRVLPKMLNPYIGGPHPHVDNGPVAWLAKPFPSPRQAAEMLSPVVSIGGVPVQELEITHDRITPELLQQFNRATSLAEAQDYEQAISLLQRCAHEHPTVAAVHCNLGVALQLAGRVQDAYQPLQTAFDLAPQNPAVQFNLSMAELQLGHYQNGWRHYEARWSSGQGGALPKGLESWGVPASDAIAEGSTLLVYGEQGIGDEIMFFSLLKRLQATMPSVQLVVACDPRLVGLLRRSYPTLTVISSQNLSALEYRRLAASVTCRIPCGSLPGMLRFPDEVSDHDRQERTLSVDPLRVEYWRQELRRRAGKEVNEFVGVSWAGGKNVQEHAVRSIPLPAWGEIFEPSPNAQFVNLQYGVSRTVSEDSQPEQVGQAFLANMITADQIAPLVDLEEFAAMISALDRVVSIDNSTLHLAGALGIPTVGILPVASSAAYRWGTKTEATIWYPSVRLVRRKLGESDSEVICRAAKALE
>NZ_CP036262.1|WP_145354063.1|5962542_5964468_-|hypothetical-protein
MSLQSRLYTSSKRTRKPANRLRKSQLERLESRDLFAVDIVFDYSYDDGGFFTSEAKAAIERAAEAYELRLQDTLAAIPSAPPGNSWSAVFDDPETGGSVSVPGLELAVGEVRVYLGARAIGGSTLGIASTGYSLSYNNTDWLDTVVLRGQIGDNEQSTWGGSISFDSSTSWHFGEAEPSGSQNDLYSVALHELGHLFGIANQVGNTWTNYVKPLAELSGAEQTAVNNEPGYYFTGPKSVALYGSPILVGSGHFGDDVGVGGQEAALTPSLTTGTRKPMSPLDWAALDDIGWEVSAEFVSQDLVALNGTGQWYAISDEGGAAFVRQVGSWAPGVTWGNVTVGDFDGDGVDDVIARNMNTNAWVVGERSSTGLLFRTVGVWSTAVAWENMTVSDFNGDGKVDVAARGNNGTWVVGVSDGTQIATTVYGAWTDAIQWVDVLPADINGDGQVDIIGRNQNAGGWIVAESQGTSFTNRTLGYWSPSITWTNVMVDDFNGDGMDDIYARGAGGRWIVSQSTGTAITTRTVGGWAEAINWQDIQTLDLNGDGYAELIARNSSNVWIASFFDDDIFRTVTLGAWSTSTPITFLGVADTNGDGKAELIGTTAAGSLLLSGIDGSEQLTNEVWGTWAGAVDVIFAKRGAGA
>NZ_CP036262.1|WP_145354062.1|5960616_5962536_+|asparagine-synthase-(glutamine-hydrolyzing)
MCGIAGLSGDFIPGLMDRMNTAQRHRGPDGQGVFENPASEIALGHVRLAVLDLSESSSQPMHSSDGRYVLVFNGEIYNFRELRQTLESQGVAFRSRGDTEVLLRGLQAEGTAFIKKLDGMFAFALWDQEQQELLIARDRLGVKPLYYAEPVPGAFLFASEIKAMCAHPKLRREPDFFAIQQHLAYGHSSGTRTALRGIQRVPPGGIIRWRPNQPLKTEQYWTPPFCDQPQNFKDAKEQLRELISAAVHRQLVSDVPVGAFLSGGLDSSLIARLASEQGVLNCYTTTYSSADNQLDQSASDLPYARFMAKELGARLEEIAMTSDVASIWQRLIYHLDEPLADPAAIACYLISRLAKEDNTTVMLSGQGADELLAGYPRYWAIQSTQQIDSLPMAMRSAITRMASVIPGALPGRIGGTLRRVRRVLSEAQRTPIERFLGYCSATPSASIRSILSPDFLAAIGDETALDECARGIRNDPSAQNINRFLRRDLGTYLPNHNLLYTDKMGMATGIETRVPFIDNALVDFIVGLPPELKIQKGTTKFLLKEAARTLVPDRVIDRRKAGFGAPYRNWLRNDLSEMWNDLTDSESVNRRGWFDPQALAEIRHQSQTGKTDLYMLQWAVLTMELWARQFIDQNPADQN
>NZ_CP036262.1|WP_145354071.1|5983898_5984903_-|aspartate-semialdehyde-dehydrogenase
MYENLALVGATGAVGRIVLDQLVQRQLPYKTLKLLASSRSAGTQVKVGDETKTVELLEPSAFDGVDLVIASTPDEVSAEFCSWAVERGAVVVDESAFWRMDPKVPLIVPEVNPEAIKGHHGIIASPNCSTTQMVVAMAPIYRAAGIRRVVVSTYQATSGAGLAGNVELEKATQAALSKQGNHTAETFQHDIAFNLIPQIGSEKHEGYTSEEMKMVYETRKIFGDDSIQVCPTCVRVPVMIGHSESILIETEKPLSAAEARELFAAAPGIRVIDDLSQKSYPMPRDCDGCDDVLIGRIRKDLSSENGIAFWCVSDNLRKGAATNAIQIAELLMKS
>NZ_CP036262.1|WP_145354072.1|5985090_5986281_-|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme
MRDRTSFLTILLTAVATLGLGGWVAAEETPGISKEKPAEGPFVEVKEGYMVPYTTRIPGSDVTFEMVPIPGGTYMLGSPESDPAHKEDEGPQVKVTIDPIWVARHEITWDEYDQYMNLYYTFKEFQARGIRPVDPEQRADVITSPTELYQPDHTYEYGKEPDEPAITMTQYAAKQYTKWLSAITGQQFRLPSEAEWEYACRAGTETPYNFGDSADDLDANAWFFDNAEEGVVKVGQKKPNAFGLYDMHGNAAEWVVDGYTEDGYKSLAGKELNGINAVQWPTSAYPRVVRGGSWESDPEDLRSTSRMGSQDPEWKEEDPNFPKSPWWFTSDPARGVGFRIVRSYQPLAPETISKFWEAVTEDEIDDIESRLREGRGGLGKVDKGLTKAIEDWKASQ
>NZ_CP036262.1|WP_145354073.1|5986421_5987795_-|O-antigen-ligase-family-protein
MAKLSFLTLVIAAAVNPVNLMTSIEFERQTQSNSPILLAKLCVAGVAALLGVWIWFTSPSVRRSMFSIPGACLVALAIVFCLTSLFAGVGSPANPMISRAAAMIFVAYLLFTLGAVQRLQPHSFLLALLLGVVANLLVTLALYVFVPSHGVFHEYISATETVPRMGGTAHPNGVAITAVTAVLIALGIRFGRPRGEGRGSLQRDAETERAVSTPWEISVGSQSLRLNRWLVFAVLIGVVAALAALSRTAILAGGIATCFLLFHWFSRRAIVLSVVLLITLGIGTALLTSMSTGKDPFSSSAVVAVTKSGKLEELTSMTGRTVIWAQAIDWIQQRPWTGWGLDSSASVMTGPTAGTHNLMLNTCFSAGLVAGGILLVLLLWSLRSAFVQPYPWIRGILIYVLVSGLVEDTIFDSFPNALSLAWIAALVAPSMYSASLKDEEGSGGVDPLSTPTRSLGG
>NZ_CP036262.1|WP_145354074.1|5988097_5989519_-|trypsin-like-serine-protease
MHPYRPDTPNIVPASDTGPASDAGPASDIVLSADIVTSAEGVTPASSSPSESPSESSEVSVSIRGERVGFGYENPLPARQRDRNRDSKGSLSQSVLFLMTVALLFAALRYLLPVVVEEARYAWHRGELRAEYEVSGEGLRTASLDSLSQASQMVTQHVGPSVVHIEVQRQRTSQQVDLANFLQEQKGLPPSMGPLLSSDQGSGVIVDASGYILTNEHVIAGGASIQVGLSDGQRVPAVVVGVDPLTDLAVLKIDATNLIPIEFGESDAAKVGSPVWAVGSPFGLDRTVTFGILSGKHRVVKASTRYQDFMQSDVAVNPGNSGGPLVDARGQLIGINTAIVGDTYRGVSFSIPSNVAKSVYERIRADGHFQRGWLGVALAEVPDDLHKGADARVRGALVTGLADPDSPAARAGVLAGDIVLQLNEIELADIGHLMRLVGDLKVGESVQLLVRRDDGLQSLWVTIGSPPAERVLR
>NZ_CP036262.1|WP_145354075.1|5989939_5992426_+|glucuronate-isomerase
MSDSLRQTIYQALADTCLIDPHTHINPHSPASSTLADVLGYHYYTELAHSAGMPREHIEAANLGPKEKVERLVHGLAPLENTAQYSWLIAICQRFFGFEEDKLTPDNWEAVYDAAEEKMRIAEWPDLVLEKSNVEAVFLTNDFDDALEGFDTNKYIPCLRTDDLVFHLGKPEVRERLAACSGIEVSDLGTLREALQQRFEHFTRNGARACAISLPPSFSPTQVTDGRAATALDDVLRSGTSAAPAHQDALARRVFWTLAELCDEYNLPFDLMIGVNRGVYPAGVYQGQDLYDSRVSLIQYRELFNAFPEVKFPISVLASVTNQELVSYAWIFPNVLTNGHWWYSNTPSFIERDATARLEAVPQTKQIGYYSDAYKLEFVWPKFDMYRQILAKILTESFVIARGWSEERAIALGKQILRGNVETIFPAREPSPPAEEAVPSDSSTADSWDIAGATGAAVIAPAAGAIAGVFTEPYQASEIEKEAEIEAEIEEAAEEIEAAAEAQIEQAVEEIEEAAEAEIEEAAEEIEEALYDADGDDDEPMEFATIDSSEDMTPEPEVAFDTDQEVADEEDDAELWTGPEETLEVATEENSIEIKDPLAELETESPGLETELSAAEIELSEPEGDRSEPAVELPELETESLVLETESLDIDVSLPETETDPLALAPEATETTETTEAASEIVFDLDQEASDEEDDDELWTGAEESLEIESAEPESPTAEATPEIVFDSDQEASDEEDDALLWGTDSDDEEDEDSEGDLTIEPPFNEPPPTELPGLEEYTELNDSGTVMPPDDSEEEGFGLLSDGSSVFESDEENTDSEDDGKDTPSPN
>NZ_CP036262.1|WP_145354076.1|5992523_5994818_+|ribonuclease-R
MEVSKELTDRVLQLIHSPNYQPGKPKQLASALKLDAEETRELKRVIKWLAAQGQLAYGSNHMIISPALARGNIDIVRGSFRPAVGGFGFVRPNSGGTETEAPDDIFIPPGETLGALYGDVVEIRVRGRSNRRGNGMEGTVLKIIERSRRQFTGSYRLENGESMVYLDGVPYEAPISVGDVRGLPVENDDKVVVEMVEFPDAQGKGGEAVIMEVLGSSKNPAIDTIMIMRQYGLPDAFPEAVIDAARAESDRFDDSKVPAERKDLTDLLTITIDPFDARDFDDAISLKHADGRWTLWVHIADVSSFVPAGGPIDAEAYKRGTSVYLPGRVIPMIPEIISNHMASLQPEQIRFTKTVEIEMLDDGTVTSTEVYNAAIRSDKRLNYEQVDQFIANPDDARKEWGEPIVDLLAHMYNLAMTLRKRRLDRGALTMDMPDIKLNLDKQGKVKGAFLAVNTESHQIIEEFMLAGNQAVATWLDDLELNFLHRIHPAPERRKLRQLQQFVKDIGIQVDTLESRFEIQKVLSTVAGGPLEHAVNFAVLRAMNKAIYGPHRDGHYALDMQHYCHFTSPIRRYPDLMVHRLVQKIIDKVPTPDDPFPVLLRDGHHCSDQERNAERAERELIQVKLLHHLKKHVGEKMEAVISRVYPDGLNARCLKLPIEGFIPITALPNDNYRYERRGQVIEGHKELNRFRLGDQLTIQIAKVDVRERQLFLSVIKNHTVAREGKKTPVKKPGKAKAFGGTSKTGTKKNQSKHARTGKKNKTRRR
>NZ_CP036262.1|WP_145354077.1|5995378_5996323_+|DUF1559-domain-containing-protein
MNRHSSRAGFTLVELLVVIAIIGVLVGLLLPAVQAAREAARRMQCGNNLKQMTLACHNYHDTFGKLPAGKITTVTGFGGPYRSNWAIAILPYIEQNNLYELYRQEENNNSTWNMANVNSQFVETYACPSDLNVKQTGRPESGRGSGQDWARGSYRCMTGASAGHKDVTNGGWWDGDEYSGIPSSWIGAMHFVDEQLQQESMGITDGTSNTLLIGELHRPKDKDRRGTFWAYSYTSYNASGAVPYGASIAAHRWAECLANVPSSNICKRGFGSYHPAGNNWAVCDGSVRFISDTVNMDVYVGLASAYGGEVVQFP
>NZ_CP036262.1|WP_145354078.1|5996553_5996949_+|hypothetical-protein
MASCLCTLAVGCGPSYTTVPVSGTVTVNGKPAANVWLQFELIENGVNAPRSTATTDDSGKFTLSLATEDGGVGAVPGEHVVRLAPKGEDNEAMEGPEADAPRKMRLPEEATGGKIKFTIPEEGTDSANFDF
>NZ_CP036262.1|WP_145354079.1|5997437_6001253_-|DUF1553-domain-containing-protein
MRKIDRGTCLPAFEAFRVLLDAHRISGFVRMVGNSVSRLHSMYLPPAMNRYCTGVLRTLSAFLLCVLPAFEGALCLDVAAAEPAETDTPQPVAKWDFETPLSVKLVGGGQIQESSLIAPEFPDFQEQHQSLHLGLGSYLRIADHPDGRFDFASGDEITLEAWVRLDGFGQNAYLIGKGRTGNPGTTANNQSWALRLRSKGGSACVNFLFRSRPSADAPDSEGQWHRWTSNQGFTPGSGWHHVAVTYRFGDSDPNNIRGYLDGKQVAGRWDMDGATSRPPVNDDDEVWIGSTMKGDKSNSLHGDIDGIAVYRKVLPPETFKARYRYNPQPRVVTEVPEGKVAVQMYGPIASTGTIPTRVGKLLTTWIQDDLAFVQLPHRYDEWGIRQDWGRPLLVQATTDVAVPAGKHRILVRARGLSRLWIDDELVLTTRAQPNRAGAHHVVDPLPEVLFPGMRPHAMSEQEKVIEHTFEGQPSRFVLESIVGGPRYRPEFGENCVAIELEGTSMFTILAPQPVHPLTDEGWEAVVEKTAQQISQQDLQNRRKASEASKAYWDKRHRFAVQNRMSDTPAEQGIDGLLAARLSSELQRAAGSEAASDDQNLFAEQIEPILAQHCYRCHGEKEQGGLSLRSREKMLAGGESEIPAVVPGKPEESQLFELVSAAADDYRMPPQGDGLTEKQVAAVRTWIEQGAVVPAKPITATAEVTPVSSDEVFLRRVYLDTVGVAPSISEATEFLSSTDPDRRRKLIDQLLKDPRVADNWVGYWQDALAENPNLLKPTLNNTGPFRWWIHEALTDNKPLDRFATELIMMRGSTWDGGTAGFAVASQNDAPMAAKAYVLGTAFMGVQMKCARCHDAPYHQWKQGDLFQMAAMLERKPIKLPASSTVPPAFFAAQERESLIKATLQPGEAVQPEWPFADIIPDVPGELLENPDDSRERLAAQLTLSRRFAQIMVNRVWGRLMGLALVEPVDDWEGNPPSDPALLEYLADELIQSGYDFRHLCRTIMNSEAYQRTAIDREEGIEPESRFYAGPYRRRMTAEQVVDTAFHAVGMPLGTEELTMDVEGTLPPSTFLNFGYPERAWEFTTLANERDRPSLALPKTQAVADVLKAFGWRNSRPEPIAERELAANLIQPAVLANGTLGTWLTRLSEESGLTTEVLRDQPLETLVDRLFLTMLTRYPTDAEQARFVALLEEGYADRMVPLAEVDPLPEQERFRFVSWSNHLNSEANKIKVEMEERVRQGPPATPFIRAEWRTKFEDAVWSLLNAPEMVMIP
>NZ_CP036262.1|WP_145354080.1|6001212_6001971_-|hypothetical-protein
MYSRFDRLSRFPCKGFLSGFAACILAGISLTSAGFAQSIQGQGFAQSETQEATRYRPADEVVLARPGDRVTLVNAQDAGHDQAAASPFRGEAAPASRDVSPFRSVETNPDEEKQARQTLPLATVISSLAIVLGLFAALVWVWRRGGGSTLGGLSKEAFQVIGRSPLAPRQNMVLVRCGRRVLVLAVSGTSTSTLAEITDPDEVAELLALTGGGVGHHQFQQTLAELGKERPQQKRFVDTDEEDRPRHLFASV

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Crispr_ID: NZ_CP036262_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_18

6007305-6007410

Orphan

Consensus_repeat	Method
AGGCGTTTTACTAGCCCAGCGGGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_18

>merge|NZ_CP036262|18|6007305-6007410|CRISPRCasFinder
AGGCGTTTTACTAGCCCAGCGGGCGGGTACTTGCAGGGATAAAGAACCTCTCTGAGCTATAGCACTCACACCGAAACATACGAGGCGTTTTATTAGCCCAGCGGGC

>NZ_CP036262|18|14|6007305-6007410|CRISPRCasFinder
AGGCGTTTTACTAGCCCAGCGGGC	GGGTACTTGCAGGGATAAAGAACCTCTCTGAGCTATAGCACTCACACCGAAACATACG
AGGCGTTTTATTAGCCCAGCGGGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354078.1\|5996553_5996949_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366443
NZ_CP036262.1\|WP_145354085.1\|6005222_6005864_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235774
NZ_CP036262.1\|WP_145354083.1\|6003790_6004552_-\|motility-protein-A	unknown	unknown	gnl\|CDD\|224210
NZ_CP036262.1\|WP_145354096.1\|6017796_6017976_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354086.1\|6006090_6007281_+\|N-acylglucosamine-2-epimerase	unknown	unknown	gnl\|CDD\|238153
NZ_CP036262.1\|WP_145354084.1\|6004610_6004805_-\|flagellar-protein	unknown	unknown	gnl\|CDD\|377645
NZ_CP036262.1\|WP_145354090.1\|6011399_6012620_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|223282
NZ_CP036262.1\|WP_145354089.1\|6009801_6011400_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036262.1\|WP_145354088.1\|6008780_6009629_-\|DUF2064-domain-containing-protein	unknown	unknown	gnl\|CDD\|275102
NZ_CP036262.1\|WP_145355765.1\|6001970_6002372_-\|flagellar-motor-switch-protein-FliN	unknown	unknown	gnl\|CDD\|131533
NZ_CP036262.1\|WP_145354087.1\|6007502_6008711_-\|glycine-oxidase-ThiO	unknown	unknown	gnl\|CDD\|274092
NZ_CP036262.1\|WP_145354081.1\|6002456_6003005_-\|dihydrolipoamide-acetyltransferase	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354095.1\|6017090_6017597_+\|transcriptional-repressor	unknown	unknown	gnl\|CDD\|133478
NZ_CP036262.1\|WP_145354094.1\|6016626_6016929_+\|flagellar-biosynthesis-anti-sigma-factor-FlgM	unknown	unknown	gnl\|CDD\|377300
NZ_CP036262.1\|WP_145354092.1\|6013328_6015164_+\|TIGR03960-family-B12-binding-radical-SAM-protein	unknown	unknown	gnl\|CDD\|188475
NZ_CP036262.1\|WP_145354093.1\|6015267_6016200_-\|cation-diffusion-facilitator-family-transporter	unknown	unknown	gnl\|CDD\|223131
NZ_CP036262.1\|WP_145354079.1\|5997437_6001253_-\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377876
NZ_CP036262.1\|WP_145354091.1\|6012904_6013216_-\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|225057
NZ_CP036262.1\|WP_145354080.1\|6001212_6001971_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225731
NZ_CP036262.1\|WP_145354082.1\|6003004_6003784_-\|OmpA-family-protein	unknown	unknown	gnl\|CDD\|235887

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354078.1\|5996553_5996949_+\|hypothetical-protein	gnl\|CDD\|366443	pfam01060, TTR-52, Transthyretin-like family. TTR-52 was called family 2 in, and has weak similarity to transthyretin (formerly called pre-albumin) which transports thyroid hormones. The specific function of this protein is as a bridging molecule in apoptosis cross-linking dying cells to phagocytes. TTR-52 bridges by cross-linking surface-exposed phosphatidylserine (PtdSer) on apoptotic cells to the CED-1 receptor, a transmembrane receptor, on phagocytes. TTR-52 has an open beta-barrel-like structure.	0.000809107
NZ_CP036262.1\|WP_145354085.1\|6005222_6005864_-\|hypothetical-protein	gnl\|CDD\|235774	PRK06292, PRK06292, dihydrolipoamide dehydrogenase; Validated.	8.73578e-05
NZ_CP036262.1\|WP_145354083.1\|6003790_6004552_-\|motility-protein-A	gnl\|CDD\|224210	COG1291, MotA, Flagellar motor component [Cell motility and secretion].	4.40306e-80
NZ_CP036262.1\|WP_145354086.1\|6006090_6007281_+\|N-acylglucosamine-2-epimerase	gnl\|CDD\|238153	cd00249, AGE, AGE domain; N-acyl-D-glucosamine 2-epimerase domain; Responsible for intermediate epimerization during biosynthesis of N-acetylneuraminic acid. Catalytic mechanism is believed to be via nucleotide elimination and readdition and is ATP modulated. AGE is structurally and mechanistically distinct from the other four types of epimerases. The AGE domain monomer is composed of an alpha(6)/alpha(6)-barrel, the structure of which is also found in glucoamylase and cellulase. The active form is a homodimer. The alignment also contains subtype III mannose 6-phosphate isomerases.	1.84854e-64
NZ_CP036262.1\|WP_145354084.1\|6004610_6004805_-\|flagellar-protein	gnl\|CDD\|377645	pfam06289, FlbD, Flagellar protein (FlbD). This family consists of several bacterial FlbD flagellar proteins. The exact function of this family is unknown.	1.50524e-27
NZ_CP036262.1\|WP_145354090.1\|6011399_6012620_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|223282	COG0204, PlsC, 1-acyl-sn-glycerol-3-phosphate acyltransferase [Lipid metabolism].	2.43618e-15
NZ_CP036262.1\|WP_145354089.1\|6009801_6011400_+\|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.	8.56872e-95
NZ_CP036262.1\|WP_145354088.1\|6008780_6009629_-\|DUF2064-domain-containing-protein	gnl\|CDD\|275102	TIGR04282, hypothetical_protein, transferase 1, rSAM/selenodomain-associated. Members of this protein family show strongly correlated phylogenetic distribution, and in most cases co-clustering, with an unusual radical SAM enzyme (TIGR04167) whose C-terminal pfam12345 domain often contains a selenocysteine residue. Other members of the conserved gene neighborhood include another putative glycosyltransferase, an alkylhydroperoxidase family protein (TIGR04169), and a phosphoesterase family protein (TIGR04168). The cassette is likely to be biosynthetic but its exact function is unknown. [Unknown function, Enzymes of unknown specificity].	1.85864e-53
NZ_CP036262.1\|WP_145355765.1\|6001970_6002372_-\|flagellar-motor-switch-protein-FliN	gnl\|CDD\|131533	TIGR02480, Flagellar_motor_switch_protein_FliN, flagellar motor switch protein FliN. Proteins that consist largely of the domain described by this model for this protein family can be designated flagellar motor switch protein FliN. Longer proteins in which this region is a C-terminal domain typically are designated FliY. More distantly related sequences, outside the scope of this family, are associated with type III secretion and include the surface presentation of antigens protein SpaO required or invasion of host cells by Salmonella enterica. [Cellular processes, Chemotaxis and motility].	4.40532e-31
NZ_CP036262.1\|WP_145354087.1\|6007502_6008711_-\|glycine-oxidase-ThiO	gnl\|CDD\|274092	TIGR02352, Glycine_oxidase, glycine oxidase ThiO. This family consists of the homotetrameric, FAD-dependent glycine oxidase ThiO, from species such as Bacillus subtilis that use glycine in thiamine biosynthesis. In general, members of this family will not be found in species such as E. coli that instead use tyrosine and the ThiH protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Thiamine].	6.34857e-76
NZ_CP036262.1\|WP_145354095.1\|6017090_6017597_+\|transcriptional-repressor	gnl\|CDD\|133478	cd07153, Fur_like, Ferric uptake regulator(Fur) and related metalloregulatory proteins; typically iron-dependent, DNA-binding repressors and activators. Ferric uptake regulator (Fur) and related metalloregulatory proteins are iron-dependent, DNA-binding repressors and activators mainly involved in iron metabolism. A general model for Fur repression under iron-rich conditions is that activated Fur (a dimer having one Fe2+ coordinated per monomer) binds to specific DNA sequences (Fur boxes) in the promoter region of iron-responsive genes, hindering access of RNA polymerase, and repressing transcription. Positive regulation by Fur can be direct or indirect, as in the Fur repression of an anti-sense regulatory small RNA. Some members sense metal ions other than Fe2+. For example, the zinc uptake regulator (Zur) responds to Zn2+, the manganese uptake regulator (Mur) responds to Mn2+, and the nickel uptake regulator (Nur) responds to Ni2+. Other members sense signals other than metal ions. For example, PerR, a metal-dependent sensor of hydrogen peroxide. PerR regulates DNA-binding activity through metal-based protein oxidation, and co-ordinates Mn2+ or Fe2+ at its regulatory site. Fur family proteins contain an N-terminal winged-helix DNA-binding domain followed by a dimerization domain; this CD spans both those domains.	7.41568e-34
NZ_CP036262.1\|WP_145354094.1\|6016626_6016929_+\|flagellar-biosynthesis-anti-sigma-factor-FlgM	gnl\|CDD\|377300	pfam04316, FlgM, Anti-sigma-28 factor, FlgM. FlgM binds and inhibits the activity of the transcription factor sigma 28. Inhibition of sigma 28 prevents the expression of genes from flagellar transcriptional class 3, which include genes for the filament and chemotaxis. Correctly assembled basal body-hook structures export FlgM, relieving inhibition of sigma 28 and allowing expression of class 3 genes. NMR studies show that free FlgM is mostly unfolded, which may facilitate its export. The C terminal half of FlgM adopts a tertiary structure when it binds to sigma 28. All mutations in FlgM that prevent sigma 28 inhibition affect the C-terminal domain and is the region thought to constitute the binding domain. A minimal binding domain has been identified between Glu 64 and Arg 88 in Salmonella typhimurium. The N-terminal portion remains unstructured and may be necessary for recognition by the export machinery.	3.89651e-07
NZ_CP036262.1\|WP_145354092.1\|6013328_6015164_+\|TIGR03960-family-B12-binding-radical-SAM-protein	gnl\|CDD\|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP036262.1\|WP_145354093.1\|6015267_6016200_-\|cation-diffusion-facilitator-family-transporter	gnl\|CDD\|223131	COG0053, MMT1, Predicted Co/Zn/Cd cation transporters [Inorganic ion transport and metabolism].	7.51289e-78
NZ_CP036262.1\|WP_145354079.1\|5997437_6001253_-\|DUF1553-domain-containing-protein	gnl\|CDD\|377876	pfam07587, PSD1, Protein of unknown function (DUF1553). A family of proteins found in Rhodopirellula baltica.	9.44058e-41
NZ_CP036262.1\|WP_145354091.1\|6012904_6013216_-\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|225057	COG2146, {NirD}, Ferredoxin subunits of nitrite reductase and ring-hydroxylating dioxygenases [Inorganic ion transport and metabolism / General function prediction only].	5.46403e-23
NZ_CP036262.1\|WP_145354080.1\|6001212_6001971_-\|hypothetical-protein	gnl\|CDD\|225731	COG3190, FliO, Flagellar biogenesis protein [Cell motility and secretion].	3.70364e-15
NZ_CP036262.1\|WP_145354082.1\|6003004_6003784_-\|OmpA-family-protein	gnl\|CDD\|235887	PRK06925, PRK06925, flagellar motor protein MotB.	4.54346e-19

>NZ_CP036262.1|WP_145354086.1|6006090_6007281_+|N-acylglucosamine-2-epimerase
MAYAPHPSLPTASLLSTYRDGLLENTLPFWLNHACDQQHGGFFGSLDERGQVIDTDKSIWQQGRFTWLLAELANNLSPDPTWVQWAKSGADFLDTHGFDPEDGRMFFQVTRDGIPLRKRRYSFSEAFAAIAYGELAQLFNDTNYRDKALACFQTFQNHLANPPGPAKFTNARPTRGIGGAMITINIAQQLRESIKLESANAIIDQAIAEIETFHVHNDIECVVETVSPEGKRIDHFDGRTLNPGHAIEAAWFIMWEGKVRQDSRLIELGCRMLDWMWERGWDQEFGGILYFTSLDEAPIQEYWQDMKFWWPHNETIIATLLAAILTGDPKYVRWHQQVHDWSYQHFADPTNGEWFGYLRRDGAISNRLKGNLWKGPFHLPRMEWICWQMLAELPAS
>NZ_CP036262.1|WP_145354085.1|6005222_6005864_-|hypothetical-protein
MMSENDEILEPPGSIAIIGGGILGLEAALYGRFLGYDVQVFEAARIGQWWEEQGDVELGFLPGRAISGLAWQAIQAQRDQPEELPVLPTTMAEWGSQIVQELAEVDLLRGRVLASHRVTEVTAVPNEEDPNETDFVIRCDGAEESWEAEAIIDTTGLFSPAEGEALVPYRYRLTQPSDNDFETKTATGRDQICQLFAQLGDRPDLDLFRPTRT
>NZ_CP036262.1|WP_145354084.1|6004610_6004805_-|flagellar-protein
MIKLSRLDGEPFILNADLIRYVESRPDTFITLTTGERLVVAESMDEVVDRSVRYQQQKQWIPGR
>NZ_CP036262.1|WP_145354083.1|6003790_6004552_-|motility-protein-A
MDIASLIGLILAVGLIVGSMLMGSAPMTAFVDIPSFLVVVGGAVAAAMICFPLKSMLGVPKVMMKVFLNKNEDVSKLIQQIVALAETARRDGLLALEAQISDIENPLVKTGLQMAVDGSTPETVEEVLRTEVNAISTRHREGKSVMDQLGRFAPAYGMIGTLMGLIMMLSDMSDPSGIGAGMAVALITTLYGAIVANVVFSPFAEKLGLLSRKEMIGMEIAIRGVMAIQSGESPRAIDQKLQTFLPPKLRSKE
>NZ_CP036262.1|WP_145354082.1|6003004_6003784_-|OmpA-family-protein
MEEEPEESGPEIPEWVVTFGDMMSLLLTFFIMLVSLSEIKEDEKYQALVDSMHRQFGYSKSLDSLAPGDAKPRASAMSVLATTGRAKRKDTAKGGVPEPAPHGEEPMVRIIRPGKRTAVGAVVFFEVGDADLDAEGKRVLDQVSVQLRGKPQKIEIRGHASPELAARTGDVNEAMDLGYLRARHVLDYLVNVTELDAKRFRLNSAGATEPMHSGGDSANGHANARVEVFLLDENAEDLRGTSAERAQRVLQTPTNDEAP
>NZ_CP036262.1|WP_145354081.1|6002456_6003005_-|dihydrolipoamide-acetyltransferase
MADDAPENEEVAAPKKSGLGKGLMIGFISVVVLVETALFFFLVPSAEEVSALAEARLIQSVQEGQQKVEELTDEENSVEEVLIGQFGETFSPLDTQDHYRVELNLFGLVRKKDLEKMNAEKTSKEGRIRHAVRMKIRMSDLSELDENQLGLLQRRILTTCNHLLEDDLLLSVGFRDYQLYKE
>NZ_CP036262.1|WP_145355765.1|6001970_6002372_-|flagellar-motor-switch-protein-FliN
MATDKKQEVSPHDIEKLIADAQAGVDQAVGNDPDSDAQPFHLNNLESVAQGGETHPMQLLGDVELDLRIELGRTQMRLEEVLKLRGGAVVALDKLAGDPVDVYVNGRLIARGEVLVMNDNFCVRVTELLGATA
>NZ_CP036262.1|WP_145354080.1|6001212_6001971_-|hypothetical-protein
MYSRFDRLSRFPCKGFLSGFAACILAGISLTSAGFAQSIQGQGFAQSETQEATRYRPADEVVLARPGDRVTLVNAQDAGHDQAAASPFRGEAAPASRDVSPFRSVETNPDEEKQARQTLPLATVISSLAIVLGLFAALVWVWRRGGGSTLGGLSKEAFQVIGRSPLAPRQNMVLVRCGRRVLVLAVSGTSTSTLAEITDPDEVAELLALTGGGVGHHQFQQTLAELGKERPQQKRFVDTDEEDRPRHLFASV
>NZ_CP036262.1|WP_145354079.1|5997437_6001253_-|DUF1553-domain-containing-protein
MRKIDRGTCLPAFEAFRVLLDAHRISGFVRMVGNSVSRLHSMYLPPAMNRYCTGVLRTLSAFLLCVLPAFEGALCLDVAAAEPAETDTPQPVAKWDFETPLSVKLVGGGQIQESSLIAPEFPDFQEQHQSLHLGLGSYLRIADHPDGRFDFASGDEITLEAWVRLDGFGQNAYLIGKGRTGNPGTTANNQSWALRLRSKGGSACVNFLFRSRPSADAPDSEGQWHRWTSNQGFTPGSGWHHVAVTYRFGDSDPNNIRGYLDGKQVAGRWDMDGATSRPPVNDDDEVWIGSTMKGDKSNSLHGDIDGIAVYRKVLPPETFKARYRYNPQPRVVTEVPEGKVAVQMYGPIASTGTIPTRVGKLLTTWIQDDLAFVQLPHRYDEWGIRQDWGRPLLVQATTDVAVPAGKHRILVRARGLSRLWIDDELVLTTRAQPNRAGAHHVVDPLPEVLFPGMRPHAMSEQEKVIEHTFEGQPSRFVLESIVGGPRYRPEFGENCVAIELEGTSMFTILAPQPVHPLTDEGWEAVVEKTAQQISQQDLQNRRKASEASKAYWDKRHRFAVQNRMSDTPAEQGIDGLLAARLSSELQRAAGSEAASDDQNLFAEQIEPILAQHCYRCHGEKEQGGLSLRSREKMLAGGESEIPAVVPGKPEESQLFELVSAAADDYRMPPQGDGLTEKQVAAVRTWIEQGAVVPAKPITATAEVTPVSSDEVFLRRVYLDTVGVAPSISEATEFLSSTDPDRRRKLIDQLLKDPRVADNWVGYWQDALAENPNLLKPTLNNTGPFRWWIHEALTDNKPLDRFATELIMMRGSTWDGGTAGFAVASQNDAPMAAKAYVLGTAFMGVQMKCARCHDAPYHQWKQGDLFQMAAMLERKPIKLPASSTVPPAFFAAQERESLIKATLQPGEAVQPEWPFADIIPDVPGELLENPDDSRERLAAQLTLSRRFAQIMVNRVWGRLMGLALVEPVDDWEGNPPSDPALLEYLADELIQSGYDFRHLCRTIMNSEAYQRTAIDREEGIEPESRFYAGPYRRRMTAEQVVDTAFHAVGMPLGTEELTMDVEGTLPPSTFLNFGYPERAWEFTTLANERDRPSLALPKTQAVADVLKAFGWRNSRPEPIAERELAANLIQPAVLANGTLGTWLTRLSEESGLTTEVLRDQPLETLVDRLFLTMLTRYPTDAEQARFVALLEEGYADRMVPLAEVDPLPEQERFRFVSWSNHLNSEANKIKVEMEERVRQGPPATPFIRAEWRTKFEDAVWSLLNAPEMVMIP
>NZ_CP036262.1|WP_145354078.1|5996553_5996949_+|hypothetical-protein
MASCLCTLAVGCGPSYTTVPVSGTVTVNGKPAANVWLQFELIENGVNAPRSTATTDDSGKFTLSLATEDGGVGAVPGEHVVRLAPKGEDNEAMEGPEADAPRKMRLPEEATGGKIKFTIPEEGTDSANFDF
>NZ_CP036262.1|WP_145354087.1|6007502_6008711_-|glycine-oxidase-ThiO
MRIGVTVVSVHSQDDVSVPLPDRSAEGGPIQSGSEITIVGGGVVGLSVAWEAVRRGLRVTVLEKKTIGEGTSWTAAGILPPANWETATDPVDRLRGLSHSLHPVWAAELLQATGIDNGLRRCGGIYLATSVGEAAALVGLRAYWQEYDIAVEALSMTELVALEPSLTSIVEAGRVKSAYRLPDEYQIRSPDHLAALRAACELEGVEIVESICVDRLDEQPDHIGLQTAAGKRTADAVVVTAGAWSSALAKESGFPFDIIPVRGQVLMYHLSEPPFRHVVNEGNRYFVPREDGHLLIGSCEEEVGWTTETTPSALAEIQHWGEQVWPGLKSHAPMRSWAGLRPSTVDGFPYIGKVPQSRRTFVATGHFRSGIHLSCGSAVLIVDALMGEPPKMDLDPFRIGRG
>NZ_CP036262.1|WP_145354088.1|6008780_6009629_-|DUF2064-domain-containing-protein
MTPKHQNRLPSLVCLVAKYWEPGTVKTRLGADVGMPVSAALHQRFVKHLTKRLGAGLPGHSDTPPPQVQQASCQNNESAAVKQIWAISPPDAVAKVQGEVPGWEIGPQGDGDLGERLQRLFQDHLACRSQDPVEQSRMLVIGGDCPDLPAATIAEALDQLRTVDAVLGPASDGGYYLLGLKGPWQDWMKRLFQEVPWSQPEVAEVTRDRLKAAGRRWHELPCRDDVDTLADLCRLVERLQANEVESLADGDPSSERELLNEIWDCLPVALRSLPALHKLAGC
>NZ_CP036262.1|WP_145354089.1|6009801_6011400_+|protein-kinase
MTKLTSERFIELVAKSNLVDPDKSDQLVEKVREKFDGNLPDDPATMAAIFRRNKLLTEWHTDKLLTGKYKGFFLGKYKLLGHLGSGGMSSVYLGEHVQMRDRRAIKVLPRRRVNDASYLARFKNEAKAIAALNHKNIVRAYDIDNEGDLHYMVMEHVDGDDLQVRVRKEGPFDFRTAAEVIVQAAEGLQHAHDRGMIHRDVKPANLLIDSEGTIKLLDMGLALFAQDDEASLTIEHNENVLGTADYLAPEQALNSHTVDHRADIYGLGCTLYFILTGQPPFPEGSLAQRIAKHQKEMPESIRKIRTDCPGELEGMVVKMIQKDPNYRYQKASDVAEAMSRWLENSKLPAKNAKTRIAGGSDPSAAALMLGSDSSTVHVDSDLQLGKHASDQNDTLSGRTGETVAKSGNQLSASDSGRLVKVKSQSRAASDSSSSAIDLERESGYAPRMAKNTEKRGVTLPPKERFLPKKAAAKATAKGQISAKGKSPAARSPATQNQSTDPEKQIPWLLVAVFGVMLIVALAVGFALAKLTS
>NZ_CP036262.1|WP_145354090.1|6011399_6012620_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSVIVEKPYQFIPPYRGNAWPTWIQRLHIVDFYLRRKDGIVGYECRNLESVAESLNKRDGILLAPNHCRYSDPLVLGWPARELKQHVYAIASWHLFNKNAFESFAIRRMGAFSLFREGNDRQSLETAIEILNNAERPLIIFPEGTTNRTNDHLQPLLEGVAFLARTAAKRREKQSGGSVVIHPTWIKYVIQGDIHAWANQALSQLEKPLGWQRTNGRTVLQRIERLATGLLSLQEIEYTGSVHPGDLDERRKRLIATLLQRTEAEAGVTPSAEPIPVLHRVRNLRTKLLPRLLATESETEKEKIRHSLREVDMAQQLESYVTGYLVPEECTDTRILETIQRMQEDFLGDVDTSLPLKAIIEFDDAIPVPPSRAPRGQVDPILIELEQRLRVLKDRLQHEARPFVDR
>NZ_CP036262.1|WP_145354091.1|6012904_6013216_-|Rieske-2Fe-2S-domain-containing-protein
MSEFETVGKVSDFEENVGQAHPVNGRMVAVFMRNGEFSAIDDLCPHMGASLAEGHVEEDTVTCPWHAWRFCIKDGTWEDNPRVKVDSFEVRVVGEDVQVRVND
>NZ_CP036262.1|WP_145354092.1|6013328_6015164_+|TIGR03960-family-B12-binding-radical-SAM-protein
MIQIERRRFLETHVWPHVQTPAQYVGGERNIVVKDHREVSGTLCLGFPDAYTIGMSHHGLQVLYSQMNRRDDWAAERVFTPWPDMEAQLRKHQVPLYSLETFTALSDFDVVGLSLQYEISAPNVLTMLDLGGIPLESEARTMADPLVIAGGPCCQNPEPMADYFDVMVTGDGEPSLPEVCDLWLELKQQARDPSGNFLTGEAGIQQRREALAEVAKRLDYAYVPRFYAPEYQNDRLVRLERTRDDVPETIAPSVIRDLDGLQLPTKPIVPYIECVHDRIAIEIMRGCPHQCRFCQSTVIKRPLRIREVETIVSGALESYYNTGFNEISVLSLSSSDYPHFEALIHRLHEVFEPLGVNIAVPSLRVNEQLRSLPQLIGTRRRSSLTLAPEVARDDMREQIRKRIKNSDLVEGCRAAFENGFESVKLYFMCGLPGERPVDLDGIVDLAEQIATVGKEVRGRYARVTASVSNFVPKAHTPYQWNGMQRREYFHWAHKYLWSRRNIRSVNIKCHDVETSLLEGVLSRGDRRTGKAIRLAWERGARMDGWTEHLDPERWWQAITDAGLDVEQQVHEGYQLTDKLPWDHVNVKYGRAFLEKEQNRATIQLAAMANAE
>NZ_CP036262.1|WP_145354093.1|6015267_6016200_-|cation-diffusion-facilitator-family-transporter
MPFTQPPTPRERVYRDAKRAASWGLGANVLLATAKLAGGIFTGSAALLADAVNSLGDVASAFAVQGALHVAQQDEDDEHPYGHTKAESIAGLSISLLVAFSAAVLGLETIRKLGAPADPPPVLAGIIAAVCAVIKEGLYRYTKLVAKRLDSTSLWAIAWDHRSDALASGAIAIALLVAPYAGPFASQIDQVTAILVCGFLIVVGIRLFSRTAGELMDQQAGPGLTNNVRQVAEDVTGVNDIEKLRVRKSGLEFFVEIHVRVDGQMSVGEGHRIGHVVKDAILASYPRVRDVHVHIEPHVCDREHGHSGNR
>NZ_CP036262.1|WP_145354094.1|6016626_6016929_+|flagellar-biosynthesis-anti-sigma-factor-FlgM
MQIFGPIRVSTSQATQANNRITPPQPGQGSATRSAGPVDQLDISSAAKAAFGSAPTDAVAGGGEIRLDRVAEIRRAIADGSYDTPEKMDMAMSRMLDRFA
>NZ_CP036262.1|WP_145354095.1|6017090_6017597_+|transcriptional-repressor
MCVSKTGPLERVEVALQPQERFEEFLRSRGLRNTTQRRLLVEQVFSRHEHFDADGLMEQLPRKGEKDYVSRPTVYRTLKEFVDAGLLKSFQLDGRTVYEHDYGYPQHDHLYCTKCERLFEFQSDELTNLRDQVAAEQGFRVSSHRLIIQGTCQACSRQRRKKRQQDLV
>NZ_CP036262.1|WP_145354096.1|6017796_6017976_+|hypothetical-protein
MPNKENTAFPSENHETKENRDGIFVSLANRLPFLQTIATTRPSRPDMAATPRQTSQLAD

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Crispr_ID: NZ_CP036262_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_19

6067952-6068083

Orphan

Consensus_repeat	Method
GCGCCGTGCCGCTAAGAGGTCACGCAAATCCTTGCGGT	CRISPRCasFinder

1 spacers

csa3

The CRISPR arrays of NZ_CP036262_19

>merge|NZ_CP036262|19|6067952-6068083|CRISPRCasFinder
GCGCCGTGCCGCTAAGAGGTCACGCAAATCCTTGCGGTGGGGTGCGAGCCCTAAGGACCGTCGATAACTTGGCGTGCAAAAGGCCGGACGGCTTGCGCCGTGCCGCTAAGAGGTCACGCAAATCCTTGCGGT

>NZ_CP036262|19|15|6067952-6068083|CRISPRCasFinder
GCGCCGTGCCGCTAAGAGGTCACGCAAATCCTTGCGGT	GGGGTGCGAGCCCTAAGGACCGTCGATAACTTGGCGTGCAAAAGGCCGGACGGCTT
GCGCCGTGCCGCTAAGAGGTCACGCAAATCCTTGCGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354119.1\|6050559_6051234_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354127.1\|6068552_6069200_-\|protein-tyrosine-phosphatase	unknown	unknown	gnl\|CDD\|319973
NZ_CP036262.1\|WP_145354122.1\|6055767_6058746_+\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377872
NZ_CP036262.1\|WP_145354135.1\|6082633_6083503_-\|TIR-domain-containing-protein	unknown	unknown	gnl\|CDD\|227253
NZ_CP036262.1\|WP_145354131.1\|6075896_6078953_+\|RNA-directed-DNA-polymerase	unknown	unknown	gnl\|CDD\|238824
NZ_CP036262.1\|WP_145354126.1\|6066554_6067730_+\|redoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239264
NZ_CP036262.1\|WP_145354118.1\|6049163_6050063_+\|sulfotransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|366246
NZ_CP036262.1\|WP_145354128.1\|6069196_6071014_-\|arsenical-pump-driving-ATPase	unknown	unknown	gnl\|CDD\|275109
NZ_CP036262.1\|WP_145354123.1\|6058754_6060140_+\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036262.1\|WP_145354132.1\|6079306_6079849_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145355777.1\|6072625_6072910_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	csa3	COG0640_csa3_CAS-I-A	gnl\|CDD\|238042
NZ_CP036262.1\|WP_145354130.1\|6075115_6075619_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354121.1\|6054106_6055042_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|293786
NZ_CP036262.1\|WP_145354124.1\|6060546_6061662_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354129.1\|6073085_6074792_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293765
NZ_CP036262.1\|WP_145355774.1\|6062174_6064481_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293749
NZ_CP036262.1\|WP_145354120.1\|6051247_6054067_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238287
NZ_CP036262.1\|WP_145354133.1\|6079988_6081317_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214615
NZ_CP036262.1\|WP_145354125.1\|6064747_6065839_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|366359
NZ_CP036262.1\|WP_145354134.1\|6081469_6082357_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354127.1\|6068552_6069200_-\|protein-tyrosine-phosphatase	gnl\|CDD\|319973	cd16345, LMWP_ArsC, Arsenate reductase of the LMWP family. Arsenate reductase plays an important role in the reduction of intracellular arsenate to arsenite, an important step in arsenic detoxification. The reduction involves three different thiolate nucleophiles. In arsenate reductases of the LMWP family, reduction can be coupled with thioredoxin (Trx)/thioredoxin reductase (TrxR) or glutathione (GSH)/glutaredoxin (Grx).	3.12746e-09
NZ_CP036262.1\|WP_145354122.1\|6055767_6058746_+\|DUF1553-domain-containing-protein	gnl\|CDD\|377872	pfam07583, PSCyt2, Protein of unknown function (DUF1549). A family of paralogues in the planctomyces.	3.19168e-88
NZ_CP036262.1\|WP_145354135.1\|6082633_6083503_-\|TIR-domain-containing-protein	gnl\|CDD\|227253	COG4916, COG4916, Uncharacterized protein containing a TIR (Toll-Interleukin 1-resistance) domain [Function unknown].	1.58515e-31
NZ_CP036262.1\|WP_145354131.1\|6075896_6078953_+\|RNA-directed-DNA-polymerase	gnl\|CDD\|238824	cd01646, RT_Bac_retron_I, RT_Bac_retron_I: Reverse transcriptases (RTs) in bacterial retrotransposons or retrons. The polymerase reaction of this enzyme leads to the production of a unique RNA-DNA complex called msDNA (multicopy single-stranded (ss)DNA) in which a small ssDNA branches out from a small ssRNA molecule via a 2'-5'phosphodiester linkage. Bacterial retron RTs produce cDNA corresponding to only a small portion of the retron genome.	2.52485e-15
NZ_CP036262.1\|WP_145354126.1\|6066554_6067730_+\|redoxin-domain-containing-protein	gnl\|CDD\|239264	cd02966, TlpA_like_family, TlpA-like family; composed of TlpA, ResA, DsbE and similar proteins. TlpA, ResA and DsbE are bacterial protein disulfide reductases with important roles in cytochrome maturation. They are membrane-anchored proteins with a soluble TRX domain containing a CXXC motif located in the periplasm. The TRX domains of this family contain an insert, approximately 25 residues in length, which correspond to an extra alpha helix and a beta strand when compared with TRX. TlpA catalyzes an essential reaction in the biogenesis of cytochrome aa3, while ResA and DsbE are essential proteins in cytochrome c maturation. Also included in this family are proteins containing a TlpA-like TRX domain with domain architectures similar to E. coli DipZ protein, and the N-terminal TRX domain of PilB protein from Neisseria which acts as a disulfide reductase that can recylce methionine sulfoxide reductases.	8.30217e-21
NZ_CP036262.1\|WP_145354118.1\|6049163_6050063_+\|sulfotransferase-domain-containing-protein	gnl\|CDD\|366246	pfam00685, Sulfotransfer_1, Sulfotransferase domain.	9.99003e-20
NZ_CP036262.1\|WP_145354128.1\|6069196_6071014_-\|arsenical-pump-driving-ATPase	gnl\|CDD\|275109	TIGR04291, Arsenical_pump-driving_ATPase, arsenical pump-driving ATPase. The broader family (TIGR00345) to which the current family belongs consists of transport-energizing ATPases, including to TRC40/GET3 family involved in post-translational insertion of protein C-terminal transmembrane anchors into membranes from the cyotosolic face. This family, however, is restricted to ATPases that energize pumps that export arsenite (or antimonite).	0
NZ_CP036262.1\|WP_145354123.1\|6058754_6060140_+\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	3.58789e-150
NZ_CP036262.1\|WP_145355777.1\|6072625_6072910_-\|metalloregulator-ArsR/SmtB-family-transcription-factor	gnl\|CDD\|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	7.57017e-16
NZ_CP036262.1\|WP_145354121.1\|6054106_6055042_+\|hypothetical-protein	gnl\|CDD\|293786	sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.	9.9586e-05
NZ_CP036262.1\|WP_145354129.1\|6073085_6074792_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293765	cd16146, ARS_like, uncharacterized arylsulfatase. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036262.1\|WP_145355774.1\|6062174_6064481_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293749	cd16025, PAS_like, Bacterial Arylsulfatase of Pseudomonas aeruginosa and related proteins. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036262.1\|WP_145354120.1\|6051247_6054067_+\|hypothetical-protein	gnl\|CDD\|238287	cd00519, Lipase_3, Lipase (class 3). Lipases are esterases that can hydrolyze long-chain acyl-triglycerides into di- and monoglycerides, glycerol, and free fatty acids at a water/lipid interface. A typical feature of lipases is "interfacial activation," the process of becoming active at the lipid/water interface, although several examples of lipases have been identified that do not undergo interfacial activation . The active site of a lipase contains a catalytic triad consisting of Ser - His - Asp/Glu, but unlike most serine proteases, the active site is buried inside the structure. A "lid" or "flap" covers the active site, making it inaccessible to solvent and substrates. The lid opens during the process of interfacial activation, allowing the lipid substrate access to the active site. .	2.46821e-06
NZ_CP036262.1\|WP_145354133.1\|6079988_6081317_-\|hypothetical-protein	gnl\|CDD\|214615	smart00318, SNc, Staphylococcal nuclease homologues.	5.05137e-26
NZ_CP036262.1\|WP_145354125.1\|6064747_6065839_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|366359	pfam00891, Methyltransf_2, O-methyltransferase. This family includes a range of O-methyltransferases. These enzymes utilize S-adenosyl methionine.	3.37837e-18

>NZ_CP036262.1|WP_145354126.1|6066554_6067730_+|redoxin-domain-containing-protein
MSKFSRPFQLLSAICVVPLLTLSSAVLAADGPTMTIGSKAPAIDIEHWVSDGKGQFPHTTKLESGKVYIVEFWATWCGPCIAAMPHLSETQQKYADQGVQLISVSREPLETVETFLEKPVRNEEDKTYRELTSTYSLTCDPDRSTFEDYFQAAGQTGIPCAFIVGKSGLIEWIGHPMRMEEPLEQVLADKWDREAFGVEFAAAQKKKWLQAELSRNFRTALNLANAGKSDEAIKIFDTLIANEEYEAQHGRLKQARAGILITTAGEDAEPLMTQYIADHGDDASALAAISRDVLTAKLQRKELPDSVFALAAEAANKAVESNPNELGFLYLLAQWQKANGETEQAIKTTETAIELATKQNSRLAGMLTQFLATLKPKQETPAKESEPAEEK
>NZ_CP036262.1|WP_145354125.1|6064747_6065839_+|methyltransferase-domain-containing-protein
MNDLRLNNLPQSDPANVLRFRDRQYAADLIGAAIIEFDFFSWLQDNPRSSLSVICEHFDWHARPADVLLTLCRASGFITSEEICDGNYRADDSGLSSLSIVGQEHLTSTSPWFLGPYYQPIADSKILKDFASILRTGKPANWQAKSDGADWHESMKDPQFARSFTGLMNCRGLALGQHLAKSLIPKLSESKHLLDVAGGSGIYSATMVAHNPHLRATVWEQAPVDAIVRSEIERYGLSEKVSIFSGDMFSNDWQTSLSNAPAMDVVLMSNVLHDWDWPEAQSLINKAYALLPPKGTLVIHDAIINAEKAGPLAVAEYSALLMNITQGKCYSVGEYNSMLANAGFQPAEFQSTIADRGFMTAIK
>NZ_CP036262.1|WP_145355774.1|6062174_6064481_+|sulfatase-like-hydrolase/transferase
MQQSTYNPLPAENRLPDDAPNILIVLIDDVGPGQTDAFGGEIHTPTLNKISKEGVAYNRFHTTAMCSPTRAALLTGRNHHRVGNGQITELANDWDGYVGIIPKSSATVAEVLKNYGYRTAAWGKWHNTPAQQITAAGPFDFWPAGYGFEYFYGFLAGEASQYEPQLVRNTTYVDHPHTSDGHDYYHLSEDLADDAIHWLKDHKAFAPDKPFLMYWASGASHGPHQVPKEWADKYKGKFDDGWDEYRKRVYVRAKELGWIPKNAQLTPRPPTLASWDSIPEDEKPFQRRLMEVYAGFTEHADVQVGRIVDEIDNLGYGENTMIFYIWGDNGASAEGQNGTISELLAQNSIPTTTQQQIEALDSLGGLDVLGSPKTDNMYHAGWAWAGASPYQGTKLLASYFGGTRNPMAVRWPAKIKPTAKPHSQFLDVNDVVPTIYDILDITPPRMVNGVPQDKIDGISFKSTLNDASAKEVQPTQYFEIMGSRAIYHDGWIASAIGPRLPWESGLPAGIKEWNPANDKWQLYNLNEDWTQANDLADKMPAKLEEMKKLFLIELTENQGLPVGGGLWVPLLHPELRLVPPYTSWNFPVAITRMPEVAAPSLGNKDNVVTVNTDVPANANGVIYALGGFSGGLTLYVKENVLSYEYNLFEIQRTHIRAKGKLAAGKHKIEVKTTYVEPKPAGPLKVVLSVDGKEIASGIVPTSAPLLFTANDALDFGIDLGSPVGLEYYDLAPFKFNGTIKNASVKYLGTPAQIKKERGETDNQIPAAN
>NZ_CP036262.1|WP_145354124.1|6060546_6061662_+|hypothetical-protein
MLTHSFLMHGAGKMCNVNRSEVFKANEIGVYHAMNKTTRGIYLFGIDLTSENDYRDRRGWYRDRMALLARFFCIDVLAYSIMSNHWHAILRNRPDLATKLTPREVAIRWLSVTSRAKCRNKNGGKITEAEIAKIVNDPEAVEERRARLSNISWFVRQMCQTLSRRCNKEDQVTGHLFGNRFQMNRLPTEEEILAGMLYVDLNPLRAGLADALDDFAEVSISERLTTLEGEAADLESWLAPLELETEVDGKQVVVANKLTAEQIEERVRKREALSDSLGCVPMKLEAYQELLWHLALQARPELQATDRLPANIFRSPLKLAGENINIDELAERHAQMGRRYASPVDLQTRIAIAQRQAGGGSVPIDNTWASV
>NZ_CP036262.1|WP_145354123.1|6058754_6060140_+|DUF1501-domain-containing-protein
MNTHRWIDRRHFLYGAGLSAAAATCTNRLAHAATGPTVLHHPATASNVIFLFMSGGPSQVDTFDPKPELDRLEGEDVPESIAASIPRIKRAGIKNLMRSPWKFKNHGESGIPVSELFPNVAKQVDDLCVIRSMQHNNPVHGPGECVALTGTSAGDRPSIGSWSLYGLGTANENLPAFITMNLHSDGMQYPQGAGWGSGFLPSGFQGTIVDPSKGIRHVAMPPNTTEQDRRQQLDLIHWFNDRHLRQSGEQSELQARIDSYETAFRMQTAAPDLFDISKETQQTHQLYELDNPQSKSVGKACLLARRMVERGVRFVQVRVGGWDAHGNIQANHSKMASRTDGPIASLLTDLRQRDLLKSTLVVWAGEFGRTPTKEGRGKGRDHSPAGYTTWLAGGGIQGGQIIGATDPLGYVAIERPVSPHDFHATILHALGIDANRLTYNHHGRDEVPTVFGGEAVKEAFA
>NZ_CP036262.1|WP_145354122.1|6055767_6058746_+|DUF1553-domain-containing-protein
MRPTILLLSCLSALCSYFAAVLPAADKSIGWSDEWTMSQAGGVSQWFEIRGTGKRNNPLRRQLDQRFDGDQFFVRFQLRYDAASIDTPADGNGEFLVLWIDEQDGGDGAGHSGGIPNIGIHVNQNKNAFMARFSSASETFGDVELQGDRVYNVLACLSRSNPGSGNRYDQMRVWIDPKITEEAKPTIRLTGKDAIQSIHWIGFSTGGKTEPDDRISVSEVSVATSWLASFGLTLEIDRGNKPKTTSPPPSMPPANQAINQTVDFRKEVYPILRDHCFECHSGEDSESGIRLDSYDEILNQVSPRDAKSSHLIALIESSDPAIQMPPPDTAASKVSDKQIKVLRRWIDEGVSWDQKLLPSPVLDSDHWAFQPLTVPHPPATKPNTRARSPIDAFIQSKQNDLGTASTKSADWATLQRRISLDLTGLPPSAFPGLELANSHEQLDRWIDKLLASQAYGERWGRHWLDLARWGESNGHQHNRSRPHAWRYRDYVIDSFRTDKPYDLFIREQIAGDELPAASQSLQATGFLAAARYSGNELDKEIQRNDILVDVVNATAQTFLGMTMGCAQCHTHKFDPITIRDYYRFQAFFTRGQPGNLLLTRNVPDAKSWTTTRQQLLASVRARIVEKKRIAGIPEPILVTPTTIVASLNPTERQVYKDLETAIGSVPQVWGWTGANSQTTVAPHEMRSPLPNDRAAIESLKTFIRIRGDVKSVGPEVKPGWPAAFGPTPDSADSRTDLAAWMGSSDNPLTARVWVNRIWQWHFGTGIVKTSGDFGTQGTPPTHPELLDWLANELIDSGWSTQHIHRLILQSATYRQSDAFSKSHFDLDPECTTIWRWTPRRLESEAIRDSALFVAGKLEQTDGGPSVPDTADSDSFRRSVYLQQERERIAESLTLFDSPPALSTCSRRRTSTVSLQPLYLLNSEFMQNVSQAFADRLRKSTDESDYAAAAIRIALGRNAEAEEVARLNEFLSENSLESLCLAVLNLSEFLYVN
>NZ_CP036262.1|WP_145354121.1|6054106_6055042_+|hypothetical-protein
MMFIRPMTLAALLYLISPAPNANAVPRDPVKSVTILYDLPYGPVYRRGAEQETEIWKTEGWTPETFFEDPDTIALCDTISDGSPEQLKKGIANAKDLNHQGTKNFTLLHWAYLDNNIIAFRLLLEAGASPDIPLTDHIFCKRLRHYLLKGDTILFTSIQDIAWQFTILAAKHTHKPNLRNAKNDTTLLTLTRARIASSVIDSVLQAVLQTGVDINARGEFHSTAAFRAITWNRADICLSLLKAGAAPDLKHPNNLTIKSVLEFEQQHLRKKGISSADKDALEKWLNAHEKTSANPDLTQPTNKGNQGESER
>NZ_CP036262.1|WP_145354120.1|6051247_6054067_+|hypothetical-protein
MLQTPTHAVSTIYEGSSQIEVRLTLSRPLQISDFLQIQADLNFNNQNDEGETIWSNDDIIYFIGTHEVVASIGLIADDGPWPGNGRPQDDLKVTIQTSEETIESEVIVKNVPPVFASVPTVEVTEDTDGNRLLNLSVSVIDPGRQDQLRMIANWADGETTTGEWSPNSQFDMMTLTRMIPAGAALPEIYPLTLMVHDDDIEMTNGEFNPETIGLASSQITVTHVDVAYNNDDDDGNNYPDLWDRPDDNYRISGDMDPPQGDAIVPVNKPISSENDVIAYQVADIRPQMVPATEGRYILIYDPTIIRLWDSAHKTQWIKPHNSPDTTADTFGVGRPLQGIEYEGQDTVFIEGINISPSQTSIQMAWVADGWNFTSDDTLPERESDSPKQVIGDIVIVDVWGIDVDIDSDNNDGYAQPAGDRWEEYLEDNEFAIGKIIKPIQLYESFPSNLLNEQLEANYQFTPVSIRVSTGLAPETQVVISTLTTLPHSSGSIQLWTTPRNDPNRNDNLVTEGGHRISGYLSELSLNEIGYDPNSSTITLWIETTYVRDDIRTKEDLDNLSAPSNKLRIQLLGPDNLNVEDRVKWTAVKKESFYNTLSSNQTLRNAMAAELVYGNNGIYGTPHESTDYGLKLISNQNQQDLLKLMAMSHTLSKNQAQYILDSFYYRAPTTDSPNSDSIANFGAGLYLDHFSGRFILAFRGTDPEDMNDWATNFSQLTSNYSADYEMAILLTTVLQKNVPSLQLMQLTGHSLGGGLASAAAIATALHADTFNAAGITRNTLINPVTKIEHTENSFSRFDNAHLYVDSFQVWHFKTPDNEKITVPDVLSFAQNYLSIEHNGRHYLPDAIGERHYLVGTDTLDEGLEFTQDLISFMQTPDKSSIEPILIGILSIDINILGPYIYIDGELEIATLKKMVESHSFKAIYHGLLNPNAHQFTGHTF
>NZ_CP036262.1|WP_145354119.1|6050559_6051234_-|hypothetical-protein
MPVMARGESSHEGIDGSVLVGVPVGIGSAVGSGTLVKVGVPEGVGIPVGFGVPVGIGGSEEVGVPDNVGVPVEMGGSDNVGVSVGAGGSYEVGVPVEVGVPDGVGGCGEVPVGVGAPVGERAPVEEGVPVGVRLPVGFGRSEGSGMLGKVGLPVGCAVPVRVGDIVSVLVGDIVSVLVGDVGSGMQGPTILALGRQYCSPSSRSPSQSMGEESVEVVVGGVYDP
>NZ_CP036262.1|WP_145354118.1|6049163_6050063_+|sulfotransferase-domain-containing-protein
MKRLVWLASYPKSGNTWMRMLLSAYQQDRDKNFEIDDAFRSTISASRRATFLRVANKQELEIPQIDSLREAVQRSIAQTIKPPILLKTHDACVQHNGFPVIRKELTLGAIYVIRNPLDVVDSFADHMGLSTDGAISAMNNPRFSIGGKDAELVPQYLQTWSNHVRTWTEHNNFPVHVIRYEDLHAAPHFTFRNALNFLGWNVDSRRLKHAIQASSFSNLKQQEERKGFAERSQSSRSGRFFRNGKTGNWRETLTPEHIQQIVSMHGPVMEFYGYHLPCQSTDSSLTTETSNIKKQIINL
>NZ_CP036262.1|WP_145354127.1|6068552_6069200_-|protein-tyrosine-phosphatase
MNVGKPIDLYPSLSEFIAKRESEFDQIPDSRKRELKQLAGYVRDCLNAGKEADLTFVCTHNSRRSHLTQIWAKVAADALGLNVVRTFSGGTEATAMNTRVVDSLRRSGFLVTTDSAGSRDPGNPDYHVGYSDQVEPLSCFSKVYDSPPNPTEGYCAVMTCSSADQACPVVPGCELRLPIRYEDPKVADDTPQEAEVYDARSEQICREMFFAMKQV
>NZ_CP036262.1|WP_145354128.1|6069196_6071014_-|arsenical-pump-driving-ATPase
MKFLNKPTRNLFFTGKGGVGKTSMACAAAIALADRGSRVLLVSTDPASNLDEVLATELTNHPTGVESVSNLWAMNIDPELAASEYRERMVGPYRGVLPEAAVQSMEEQFSGSCTLEIAAFDEFAKLLGDASATSQFDHIVFDTAPTGHTLRLLTLPSAWSGFMDDNTSGTSCLGPLAGLQAQQAIYKQTVQSLGDAERTTLVLVTRPDLAAFREAERTSRELSELGVRQQHLIVNGVFAAEGASDPIADAMQSRCEQAINDMPTGLATLPQSTVALAPQGLVGVDALRWIGTGQSIAVQAKATNNERENLENILSQATPLQKLVDDIANQKHGVILTMGKGGVGKTTIAAAVAVSLAEKGLKVHLSTTDPAAHIAAAIASDTLEGMSVSRIDPQQEVRKYRDEVMKSAGAELDSQGRALLEEDLRSPCTEEIAVFRAFADAVAEGEDGFVVLDTAPTGHTVLLLDSALSYHREVTRQSSQMPESVEKLLPRLRDPNFTHVLVVTLPESTPVHEAEQLQKDLRRAEIEPYGWVINQSLVPLQVTDSVLLCRQHNELPFIEEVLTKHAKQTVVVPWQAEPPIGVTGLRNLVANSNGNTLTTLKGVCS
>NZ_CP036262.1|WP_145355777.1|6072625_6072910_-|metalloregulator-ArsR/SmtB-family-transcription-factor
MELQADPTADDFAKLAWAIAHPARVQIVRFLIGRQACMCGEIVNQLPLAQSTVSQHLKILKESGLIQGEVDGPKVCYCINPECLESLKAFVNEL
>NZ_CP036262.1|WP_145354129.1|6073085_6074792_+|sulfatase-like-hydrolase/transferase
MKPSHFALAILVTCTTLSLAAEDRPNVVLIMSDDQGGGDYGFMGNDVIRTPALDAMHARSGYLSKFYVSPVCAPTRASLMTGRYNYRTRCVDTYVGRAMMDPEEVTLAESLRDAGYKTGIYGKWHMGDNYPLRAMDQGFSESLVHRGGGIGQPSDPIGAEGKYTDPVLFKNGEEVSLKGYCTDIYFDAAMEFMTSSTETGKPFFAYIATNAPHGPFDDVPQELYEEYKNTDLSSLLARPLPEKRRKAEFDKLARIAAMITNIDENVARLFAKLDELGITDNTIVIYLNDNGPNTMRYVGNMRGMKSHVDDGGIRSPLLFQWPAKVQADATSDKLCAHIDVMPTILDACNVEPPHATKMDGRSFLPLLTGEDVNWPTRQVVFQSHRGNVPQLFNHFALHEDPWKLVNPSGFGNERINGVPKLELYNLSNDPRQMHNVAADHPETTKRLSQAYEAWFADVSSTREDNFAPPRIIVGTKHEPQTVLTRQDWRHATGRPWAKDSNGFWLLQAAEAGDYDIEIILDSDNHPAGTAIVSVGESQSELKLTAGQQRGHLFVIDASPDIARGWRFL
>NZ_CP036262.1|WP_145354130.1|6075115_6075619_+|hypothetical-protein
MFEKSDLTFQQMMVWERLHDGLKAIEDANDNLESRAAKIIAGSTGAIGAIAGFNLLPQSIVDTGRIESIFLAVLCASVLVLFWFAAKLWSQRSLCVPINGDVDDLYNDFIAKTQNEAFNNALIDTAKAFEHAKWVNGIKGSELRRMYIVLQSQLVIVGVGVVIKAFS
>NZ_CP036262.1|WP_145354131.1|6075896_6078953_+|RNA-directed-DNA-polymerase
MAKRSATTRMKGLPKKFFDRNDLFVAYRKAKQDVFQEKTQANRLAFSEYEKHLNANLETLHSRLTSRTVNWFRDLNFIGDVGFIPKDLHLASTASESESEPHFSQSDPDESWKRQIQAMGGENPTVSFRPMAAFTVDMYIVCTLWVNRVGAHLDACLDNTAKGSRLRRHQRSEETGTIGGLHLDAIGSFPPYYYAYKEWRDDGLKAIRLELEEDRKVIAITMDLTSFYHRIDAGFLLDDAFLEAVRFQELSGHDLTNEERLFTRQLVRAFANWGEEYADSSDAPCVGIPVGPSAPRVIANVLLAEFDQLVQQKLDPIYYARYVDDIFLVIRDHGQFNDGKDVLSHLCERIEPLDFNDDGQELHLKLRYAKDSQLVFQAKKQRIFALSGEIGHDLLDTIQSKIDEISSEWRLLPDLDVLETSPAARALAAGKRPNEDVNTLRKADDLSLNRLSFANLLRDHDQLLNYLPPSEWRSKRHEFYKFAERNVLSPSRVFGLVGYFPRLFGLAVACRDWKQAESLLKRTVRSLTTLKETTTLLTETKTSDTWKKFALTLGRVVHETLIQCYPLSGKKPSDARSVNLLAGQISELLGFESDSERLLIEQSRELFWTDLGRVPFKDGILGYMQIPKCPLPSWEGGIPDEQRERHAAIREFVKSVGQDVKKTRPLLLPTRPLSVAEITELDQSTVSDLTKLKKFVHAIRGTWVRPANDHEDGDWSTATRVTIGLGERKRQPRIAITSLAVGDSSWAMAAAGKPDLSASRYKCLTKLVNSIIKSKTRPDYVLLPELSVPRRWLPGIASKLLRQRISLIAGAEYRYDKSVVFNEAAIYLVDNRVGYASAHTVIWQQKGLPAHHEREELRSKFGLKLAEPQSSRCLKRVYNHFGFEFGTLICSELTDIEHRQIFRGQVDGLFVLSWNQDLESFGSLIESASLDVHCFMALVNNRKYGDSRVRAPYKDAWERERARIKGGMDDYFVIVELDIDAIRDFHSHQLPPLGDRAKFKPTPEGFKISKSRKRIPGT
>NZ_CP036262.1|WP_145354132.1|6079306_6079849_+|hypothetical-protein
MNLDEQFIDVRIHYFPQWDKRGDWTIAYGTTEQLRSNTGYCDTDANVIYLDGRAFPTMSADGQRAFIIHEICHDVGAAFHNRRWAIRMEHAARTADRLGESDVAEILRSDIYSYFGNGLSLAYNAEGISTYLDDLLAHNPDISFDGLRKRLSKFFGYRISKINRDFGPEIQSFADNSGIE
>NZ_CP036262.1|WP_145354133.1|6079988_6081317_-|hypothetical-protein
MGYKFGFRRSKKLPVGRLTVTHRGVSHSVRTPFGTFSNKLLGGGAKRRSQSSVSSGGNSSPSGGDALLGCFFAIFATLSFLVLGCCGFGGLVSWMASDSSTSRSQQTVADSRIGTDAVNSSALDPTASQSVATTDTSSMATESSGSLIPEAPSPSHIEVEAEDPEEPAEIQLALPKQSKRTWTDKSGTHSVVATLVNFNETHVQLERADGGNKVALPIESLSEDDQIYFAYATTPRYDQEAEVVIGKASRIMDGDTIKLHSIEDDQRTIRLVGIDAPESDQRFGPEAKLWLTHEVSGKNLRVEVKEKDRYGRLLGNVYVIDEGDRWLNHEIILAGLAWHYVDYSSDIRLAKAQQVARGEVAGLWQDARRVAPWDYRNGTRIETAIPVEAESIRTTDIQVYVTDSGTKYHSSGCRYLAKSKHQIPLSRAKSAYSPCSKCSPPR
>NZ_CP036262.1|WP_145354134.1|6081469_6082357_-|hypothetical-protein
MNDSLLAYIPDDDGYTETKTIRKVSGIHEERKLSARSSSRVLNICVRPLLFGAFAMMLNHTFREFFLEAAIESLRAVLPSPPPRRWNGKHTSILDRCIVIANYLEQEKEKDSWITPVAEDLEKLIADIKEIPGADHWLVLAEHALACFDNARVVMDDIAERLEDRQPRMLNHVPNADIAVEVVAQLAVRVDPATRKVVQVIGIVESIPCYWPESDNVIGIPLCINLNGCLDNKEAEGICIHSDAYVSEWECDTAEMEAAMAGADDDNEAEWFKHAYSNPFTVFDVDRLEPAYVPA
>NZ_CP036262.1|WP_145354135.1|6082633_6083503_-|TIR-domain-containing-protein
MPLHLIVSADPEAFTASRFEMPVERCLEYTDNNLRDYFFHFGETRIDELLAFPALIAHEQDVSDENVRLVRLTDIARRGNRIRAIFDPTGTELTYEQFTNLSFELDIDGFEYHRTHWAIKNVDLTDVLSKAGVQTPPSAFPQRPYVDLGSHRFQVALSFPGEDRNLVQDIASRLEQRLGLNSVFYDFHYQAFLARPSLDTLLQTVYTNARLNVVFLSGNYERKRWCSGIEFRAIREIIANRENDRVMFIKTGDGDVSGVFATDGWIEADNQKADNIAYFIEQRARVYDT

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Crispr_ID: NZ_CP036262_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_20

6240421-6240510

Orphan

Consensus_repeat	Method
AGAATGAATTTGCCGGTCGGCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_20

>merge|NZ_CP036262|20|6240421-6240510|CRISPRCasFinder
AGAATGAATTTGCCGGTCGGCTTTCTTAGCGGAACGGCGCGAGCCGTCCGGCCACCGCATAGAAAACAGAATGAATTTGCCGGACGGCTT

>NZ_CP036262|20|16|6240421-6240510|CRISPRCasFinder
AGAATGAATTTGCCGGTCGGCTT	TCTTAGCGGAACGGCGCGAGCCGTCCGGCCACCGCATAGAAAAC
AGAATGAATTTGCCGGACGGCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354240.1\|6243244_6244741_-\|mannitol-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|223324
NZ_CP036262.1\|WP_145354235.1\|6235010_6236342_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|274511
NZ_CP036262.1\|WP_145354245.1\|6252648_6254388_+\|matrixin-family-metalloprotease	unknown	unknown	gnl\|CDD\|239805
NZ_CP036262.1\|WP_145354241.1\|6244927_6246646_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271377
NZ_CP036262.1\|WP_145354243.1\|6248803_6249388_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238008
NZ_CP036262.1\|WP_145354233.1\|6230981_6231584_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP036262.1\|WP_145354231.1\|6225743_6227192_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293763
NZ_CP036262.1\|WP_145354236.1\|6236495_6237143_-\|DUF1579-domain-containing-protein	unknown	unknown	gnl\|CDD\|377882
NZ_CP036262.1\|WP_145355813.1\|6250383_6250623_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354230.1\|6222832_6225328_-\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377872
NZ_CP036262.1\|WP_145354234.1\|6233029_6234673_-\|phosphoglucomutase-(alpha-D-glucose-1,6-bisphosphate-dependent)	unknown	unknown	gnl\|CDD\|100094
NZ_CP036262.1\|WP_145355816.1\|6251003_6252374_+\|terpene-cyclase/mutase-family-protein	unknown	unknown	gnl\|CDD\|238362
NZ_CP036262.1\|WP_145355810.1\|6237245_6238277_-\|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|223730
NZ_CP036262.1\|WP_145354242.1\|6247031_6248342_+\|VCBS-repeat-containing-protein	unknown	unknown	gnl\|CDD\|379232
NZ_CP036262.1\|WP_145354238.1\|6240729_6241554_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354232.1\|6227668_6230983_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036262.1\|WP_145354229.1\|6221446_6222829_-\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036262.1\|WP_145354244.1\|6252343_6252547_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354239.1\|6241609_6243007_-\|glutamate-decarboxylase	unknown	unknown	gnl\|CDD\|130848
NZ_CP036262.1\|WP_145354228.1\|6220251_6221316_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354240.1\|6243244_6244741_-\|mannitol-dehydrogenase-family-protein	gnl\|CDD\|223324	COG0246, MtlD, Mannitol-1-phosphate/altronate dehydrogenases [Carbohydrate transport and metabolism].	1.3752e-169
NZ_CP036262.1\|WP_145354235.1\|6235010_6236342_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|274511	TIGR03300, assembly_YfgL, outer membrane assembly lipoprotein YfgL. Members of this protein family are YfgL, a lipoprotein component of a complex that acts protein insertion into the bacterial outer membrane. Other members of this complex are NlpB, YfiO, and YaeT. This protein contains multiple copies of a repeat that, in other contexts, are associated with binding of the coenzyme PQQ. [Protein fate, Protein and peptide secretion and trafficking].	2.62781e-19
NZ_CP036262.1\|WP_145354241.1\|6244927_6246646_-\|hypothetical-protein	gnl\|CDD\|271377	cd11484, SLC-NCS1sbd_CobB-like, nucleobase-cation-symport-1 (NCS1) transporter CobB-like; solute-binding domain. This NCS1 subfamily includes Escherichia coli CodB (cytosine permease), and the Saccharomyces cerevisiae transporters: Fcy21p (Purine-cytosine permease), and vitamin B6 transporter Tpn1. NCS1s are essential components of salvage pathways for nucleobases and related metabolites; their known substrates include allantoin, uracil, thiamine, and nicotinamide riboside. NCS1s belong to a superfamily which also contains the solute carrier 5 family sodium/glucose transporters (SLC5s), and solute carrier 6 family neurotransmitter transporters (SLC6s).	9.23528e-14
NZ_CP036262.1\|WP_145354243.1\|6248803_6249388_+\|hypothetical-protein	gnl\|CDD\|238008	cd00051, EFh, EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to the activation or inactivation of target proteins. EF-hands tend to occur in pairs or higher copy numbers.	2.61398e-05
NZ_CP036262.1\|WP_145354231.1\|6225743_6227192_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293763	cd16144, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	3.4104e-144
NZ_CP036262.1\|WP_145354236.1\|6236495_6237143_-\|DUF1579-domain-containing-protein	gnl\|CDD\|377882	pfam07617, DUF1579, Protein of unknown function (DUF1579). A family of paralogous hypothetical proteins identified in Rhodopirellula baltica that also has members in Gloeobacter violaceus, Sinorhizobium meliloti and Agrobacterium tumefaciens.	1.47671e-39
NZ_CP036262.1\|WP_145354245.1\|6252648_6254388_+\|matrixin-family-metalloprotease	gnl\|CDD\|239805	cd04278, ZnMc_MMP, Zinc-dependent metalloprotease, matrix metalloproteinase (MMP) sub-family. MMPs are responsible for a great deal of pericellular proteolysis of extracellular matrix and cell surface molecules, playing crucial roles in morphogenesis, cell fate specification, cell migration, tissue repair, tumorigenesis, gain or loss of tissue-specific functions, and apoptosis. In many instances, they are anchored to cell membranes via trans-membrane domains, and their activity is controlled via TIMPs (tissue inhibitors of metalloproteinases).	4.70612e-35
NZ_CP036262.1\|WP_145354230.1\|6222832_6225328_-\|DUF1553-domain-containing-protein	gnl\|CDD\|377872	pfam07583, PSCyt2, Protein of unknown function (DUF1549). A family of paralogues in the planctomyces.	1.88759e-106
NZ_CP036262.1\|WP_145354234.1\|6233029_6234673_-\|phosphoglucomutase-(alpha-D-glucose-1,6-bisphosphate-dependent)	gnl\|CDD\|100094	cd05801, PGM_like3, This bacterial PGM-like (phosphoglucomutase-like) protein of unknown function belongs to the alpha-D-phosphohexomutase superfamily. The alpha-D-phosphohexomutases include several related enzymes that catalyze a reversible intramolecular phosphoryl transfer on their sugar substrates. Other members of this superfamily include phosphoglucosamine mutase (PNGM), phosphoacetylglucosamine mutase (PAGM), the bacterial phosphomannomutase ManB, the bacterial phosphoglucosamine mutase GlmM, and the bifunctional phosphomannomutase/phosphoglucomutase (PMM/PGM). Each of these enzymes has four domains with a centrally located active site formed by four loops, one from each domain. All four domains are included in this alignment model.	0
NZ_CP036262.1\|WP_145355816.1\|6251003_6252374_+\|terpene-cyclase/mutase-family-protein	gnl\|CDD\|238362	cd00688, ISOPREN_C2_like, This group contains class II terpene cyclases, protein prenyltransferases beta subunit, two broadly specific proteinase inhibitors alpha2-macroglobulin (alpha (2)-M) and pregnancy zone protein (PZP) and, the C3 C4 and C5 components of vertebrate complement. Class II terpene cyclases include squalene cyclase (SQCY) and 2,3-oxidosqualene cyclase (OSQCY), these integral membrane proteins catalyze a cationic cyclization cascade converting linear triterpenes to fused ring compounds. The protein prenyltransferases include protein farnesyltransferase (FTase) and geranylgeranyltransferase types I and II (GGTase-I and GGTase-II) which catalyze the carboxyl-terminal lipidation of Ras, Rab, and several other cellular signal transduction proteins, facilitating membrane associations and specific protein-protein interactions. Alpha (2)-M is a major carrier protein in serum and involved in the immobilization and entrapment of proteases. PZP is a pregnancy associated protein. Alpha (2)-M and PZP are known to bind to and, may modulate, the activity of placental protein-14 in T-cell growth and cytokine production thereby protecting the allogeneic fetus from attack by the maternal immune system.	5.04533e-11
NZ_CP036262.1\|WP_145355810.1\|6237245_6238277_-\|alpha/beta-hydrolase-fold-domain-containing-protein	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	2.31217e-20
NZ_CP036262.1\|WP_145354242.1\|6247031_6248342_+\|VCBS-repeat-containing-protein	gnl\|CDD\|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	1.85794e-06
NZ_CP036262.1\|WP_145354229.1\|6221446_6222829_-\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	2.21115e-176
NZ_CP036262.1\|WP_145354232.1\|6227668_6230983_-\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	4.92076e-96
NZ_CP036262.1\|WP_145354239.1\|6241609_6243007_-\|glutamate-decarboxylase	gnl\|CDD\|130848	TIGR01788, Glutamate_decarboxylase_alpha_GAD-alpha., glutamate decarboxylase. This model represents the pyridoxal phosphate-dependent glutamate (alpha) decarboxylase found in bacteria (low and hi-GC gram positive, proteobacteria and cyanobacteria), plants, fungi and at least one archaon (Methanosarcina). The product of the enzyme is gamma-aminobutyrate (GABA).	0
NZ_CP036262.1\|WP_145354233.1\|6230981_6231584_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	1.43978e-24

>NZ_CP036262.1|WP_145355810.1|6237245_6238277_-|alpha/beta-hydrolase-fold-domain-containing-protein
MEKRRSSPEGKARLKQLLNRFPDADTNKDGELSWQELRTHQAASRENQAPRSQRNRALKVEAPVPDVAYGEHELQRFDLWPVPDAEAPTPLVIFIHGGGFRGGDKSLVQNSTIQTFHKAGIAVASMNYRLSDSGPYPIMMQDAARGLQTIRHRAAEWNIQPDQIGCFGGSAGAGISLWLAFHDDLADPSSDDPIARQSTRIVAAGAMNGQSTYDMHTFRDWFGVPDLEMDRALPAFLGVKTNDELDEPDVLRLMKDASPIHHLSEDDSASVYMTYSRPNVKVTKDSASSIWVHHVLLGLKLQEAMKARGLECVVTAPDMPAETEYESLEEFLIAKLKSTVGEK
>NZ_CP036262.1|WP_145354236.1|6236495_6237143_-|DUF1579-domain-containing-protein
MAMQRRMHYDLNSIAVVSPGSFLYRNSLQSMVMSMKFLGSAMVFLATVLCVSPVLLGQDTELPKPGPEFELLQADAGTWDVEIKAWQGPGEPTVSKGKETNRMLGEFWLLSNFQGNMMGLEFSGHGVYGYDQESKKYVGTWFDSLGPKKMDLVGTHDKASNTLTLEGIGPGVDGQPAKHLITTKYNDDGTHRMTMQMAVGDEMIKIFEMKYTRTK
>NZ_CP036262.1|WP_145354235.1|6235010_6236342_-|PQQ-binding-like-beta-propeller-repeat-protein
MKRSFSVVCGITVIGLATVGCGKRTPVVEVSVNDSGVTVEEIAVDGELDLAWPQWRGGVGGRANEDAATTSALPTEWNAESNVRWQADVPGRGHSSPIVVGDLVVIGSATETPAEQFVLAYDRNDGRELWKRVVHSGGLPSARAVHRKATHANGTIASDGVRLVTAHLNSDHVWATALDMEGELLWQTDIGAFVSKFGYAPSPVLYKSLVIIAADNSGGGYLVGLDVRTGEIAWRRSRGNVSSYSSPALVTVDGVDQVVISGGDRLASYAPATGEMLWETPCIAEATCGTAIATADRIYASGGYPEKETICVDGKGKQIWSNRTGLYEPSLVTDGKNLFAVSDDGVAYCWDAVDGKQHWKKRLGGNFSSSPVIAGGNVYVSDLSGNDYVFQAGAEKYQLVAKNRLGDDCYASPAVAGDAILFRVGVGQGAGRQEKLFCIANES
>NZ_CP036262.1|WP_145354234.1|6233029_6234673_-|phosphoglucomutase-(alpha-D-glucose-1,6-bisphosphate-dependent)
MTLNELAGQPVPLELLENIPRLISSYYVLKPDPKNSTQAVEFGTSGHRGTSKTGRFNEDHILAISQAICEYRKSQGITGPLYLGMDTHALSEPAFVSALEVFAANGVIAKIDADRGYTPTPVISHAILGHNRSRSIELADGVVITPSHNPPSDGGFKYNATNGGPADSATTTVIQNRANEILANGLADVKRIGFAEALASEFVQKHDYVTPYVEDLQNVVDMDAIKNANLRIGVDPMGGAGIAYWEPIAKRYGLNIEIVNRRIDPTFSFMRVDKDGKVRMDCSSPSAMAGLIDLKDRFDIAFGNDPDYDRHGIVTPSVGLMNPNHYLAVAIQYLFQNRPGWGADVAVGKTLVSSSMIDRVAADLGRTLCEVPVGFKWFVDGLLDGSLGFGGEESAGASFLRKDGTTWTTDKDGIILDLLAAEILAKTGKDPGEHYQALVEKFGSPVYDRIDAPATPAQKNALKELSPESVRSKELAGDAIEARLTEAPGNHAAIGGLKVVTQNGWFAARPSGTEDIYKIYAESFVGAEHLARIQTEAKQIVDDALSS
>NZ_CP036262.1|WP_145354233.1|6230981_6231584_+|sigma-70-family-RNA-polymerase-sigma-factor
MSNPSANRPDHPTLSTMWIADAKQMEPQAWSRLVTVFGPIVYRWCRVAGVPAGDAPDVVQEVFTSVARGIQNFERQKSSGSFRSWLATITRSRATDYFRRAAKQQQAAGGTEAMYALQQLAENVESTITPTNVQSDISKQLLLQVQAEFESTTWDAFWQTTIEGKSASEVAEATGLSRASVYQAKSRILKSLRKRLAESS
>NZ_CP036262.1|WP_145354232.1|6227668_6230983_-|protein-kinase
MFFNDRPSRRGSIFENFAIRVRRLRSSYCQVDPFSLRVLSLSPTPRENAMMTAAPTKCPPPDQLNAFVLGRLSDEASEAVYQHLSQCESCTSELETIDDGEDSLIVDLRKPDPLASFGEEPDCQVAVVKALGSLALSSDSSGIAANLPQEIGEYEIVRPLGSGGMGSVYLARHRKLGREVALKVLATHRLGDARVHQRFEAEMRAIGRLSHPNIVTAHDAREIEGTAVLVTEYIDGLDLGRLVQAVGPLSTADACEIVRVVCVALAYTHDQGFVHRDIKPSNVMLSRSGEVKLLDLGLARFQYGDPDRVEITGTGQAMGTADYMAPEQVTDSRSVDVRADIYSLGCTLMKLLTGQAPFADDQYQTPFAKMTAHVSAPPPRLSDQAGNVPKGLVSLVDSMLQKDLAKRPQSAVQVAEELEKFTEGSDLQKLIAGAHASGFSAASEPLIDSYPIANAALESTRRRVPIAFAVATGFLGFLIGIAFGVIITIKYPDGTQAKIDVPPGSEIAVESDELAGAETNPKSADATSSVVEAIGKAGQRNAVPQLLNSDSAPVTAGLAFRILLRKDDLTEEELEIATSQLGLPPSAIHMIVSVNHGDWIPIADQATAPIVREHNGIRYALASPKADQRLERTGGHVKASVSSQGLGNQKSDAVATRPEIKLAFDDALTPRMRRFTSDNLGKSLAVVVDGSVVMAPVINSPITSACVISGDFTPVEILKFYRSITAEDRTNAASKPQYSVRGTWNVLLSNGKEVQDVLIVFSNRRYYVLENSAVIQMGGYAFNSTEGVVNGQVVKVNEVFALSEFSFSAPHAGFLESKDGQAILYFEPSLLPLKVRPAFLLHKPGSTSHVTLTRQSDFPAGDNERLELVRSGVFSVAHSVGLDFCQKLDEMEEDNAIKALENQELANRRLVSQYSLKQIGIGFHNFHDVYQKFPGSANVREGARAISGDTTFPYSWRVAILPFVEQQDLFEQYRFNEPWDSENNIKLVEKMPEVYQSPFAPDDDPVGQTHFLGFATEHGALGNAHGESFRNFTDGLASTILLVESKKGVPWTKPEDLTETNVESLEGDILRYLMADGSVHDMQPIDNDKLQKLITRDGGEVIGN
>NZ_CP036262.1|WP_145354231.1|6225743_6227192_+|sulfatase-like-hydrolase/transferase
MPPAQPTSPTAVVLLTLSAVLMSVSALASDQPNIVVLFADDLGYGELGCQGNPEIPTPHIDSIAHNGVRFTDGYVAGPNCSPSRAGLLTGRIPTRFGYEFNPTGALNERPGFGLPTAEITIAEALQNAGYTTGLIGKWHQGGTADYHPFRHGFDEFFGFLQEGHYFVPPPYAGVTTMLRRKTLPYGQTGRWVGNKGLIYTDHMGYNEPDYDADNPIIRGGQPVVETEYLTDALTREAVDFIDRHDDKPFFLYLSYNAVHSPLQGSDRFMEQFASIEDDHRRIFAAMLANLDESVGAVLKRLQDSGLEENTIVFFLSDNGGPTRELTSSNLPLRGSKGDMYEGALRVPFMMQWKGKIPSGQVYRKPVSSFDIYATATANIAAATKPNQVEGVDLIPYLTGEDEGTPHKTLFWRQGGRCGLRHGDWKLVRMGGRKSPNEAKWELYDLATDLTEQKDLASSHPDQLSELVKIWEQMNHEMSEPLF
>NZ_CP036262.1|WP_145354230.1|6222832_6225328_-|DUF1553-domain-containing-protein
MRNFIDVTLLGLFAIGWGICVPSVRGAENAIDFNRDIRPILSDKCFFCHGPDAHERKADLRLDTAEGALADLGGYAAIVPGNLEESEFVLRILDQDDPMPPLDSHKSLKPSEIELLKRWIAEGGEYSEPWAYVPPERHPVPEVSDTDWPENWIDHFVLARLEAEGLQPAPDADPVTLIRRLYFDLTGLPPTPAQVDAFVNGERELTAIVDELLESPHFGERLAMYWLDLVRYADTVGYHGDQTHNISPYRDWVIAALNANMPFDQFTREQLAGDLLPNPSTAQKVASGYNRLLQTTHEGGLQLKEYDAIYNADRVRNVSAVWMGATVGCAQCHDHKYDPYTIQDHYALGAFFADIADRGFSGNTLPANRPPEISVYSLEQQQELARLKAEMALVIDEETQTQLESLESAQQKLLARIKAAKTKEAKDTLATEQKDLEQRISQLASQEKRDAFQKLRKQHRSLEKQGRQTMITVAEEPRVMRVLPRGNWQDETGDVVLPAVPGFLGRVTPTAGERANRLDLANWLVDPENGAGGLTARVFANRFWYLFFGTGISRSLADFGGQGEPPANPELLDQIAVSFYESGWDVKKLVRLIVTSHAWRQSSVASPELLERDPHNQLVARQSRYRLPAELIRDNALAVSGLLISEEGGESAKPYQPAGYYRHLNFPTRKYAAHENQNQWRRGLYVHWQRMFLHPMLKAMDAPSREECTAQRPRSNTPNAALVLLNDPTFLESARVLGARILIEGGESADSRIDFAYRVVLSRSPDEEERVVLKALLEATQAEYVSKPATADLLLQTGIAPIPDGLDKIELASWTAVSRALLNLNETVTRN
>NZ_CP036262.1|WP_145354229.1|6221446_6222829_-|DUF1501-domain-containing-protein
MNPFNRRTFLGQTGISLGSAAASTLASGAISNDIPHFAAKAKRVIFLCMAGGPSHLETFDYKPTLDELNGKPMPESFTKGQPIAQLQGQALKVLGHLADFKRYGNSGQQISDYLPHTAKIADDIAIVRSMVTEQINHDPAHTFMNTGTAISGRPSMGSWVTYGLGAETEDLPGFVVLTSQGGRNPQPIASRQWSAGFLPGRFQGVEFNSSGDPVDYVSNPKGVSANQQSALVDAIRKLDQQRNAQVANPDIDTRLSAYEMAFRMQTSVPGLMDISSEPQHVLDAYGAQPGDGTYASNCLLARRLAERGVRFIQLYHRGWDHHGDLQKYMDICCGLTDKPTAALINDLKERGMLEDTLVIWGGEFGRTPMFQGKGGPGRDHHIKGFSMWMAGGGVKGGISHGETDELGYNAVQDVVHVRDLHATMLHLLGIDSSRFSFPFQGLGMRLTGVEPAKVVHELIA
>NZ_CP036262.1|WP_145354228.1|6220251_6221316_-|hypothetical-protein
MKILFSFLSACLLISLSATAEDRLPDVEVQNVRKVSHNGEHNAFTDLIRWKDKIWLTFRSCPDGHMVFPTSKVVVMSSADEGKTWELEHRFSVEKRDVRDPHFLAFQGKLFIYTGTWYSGEGELPRDQYDLNKHLGYAVFTEDGQEWSEPHQLEGTYGHYIWRAASHDGKAYLCGRRKRNYSEDETGAGGTAIVESAMLQSEDGLNWRFHTLFQEDRGNETAFLFEPDGNMLSVSRSRTNIAVLGRSRPPYLEFSRVDLPEHIGGPLLAKWGPHTLVGGRRTTDKGPKTTLYWLKENSLIPFAQLPSGGDNSYPGFVELKDGRGLVSWYSTHEKDEKGKPYTAVYLADLELSKE
>NZ_CP036262.1|WP_145354238.1|6240729_6241554_-|hypothetical-protein
MQNDSEDCVEATGAWPFITRRVYHADGRVRVWTSRMHRKFITRLCGDGSQPIAVPQRLNQWIGGAFAIGSVCFAFASLLLLFPSLAGSFAKELNIGGIYFLGSIPFTFAAGLQLFQAANADAATEPSNRRRVLFGWRPHEIGWLSCALQFGGTILFNFNTFDAMLTSLDWLQQDVVVWAPDFFGSILFLASGYLAFVEVCHAHWAFRPRSWAWWLNFINLLGCISFMISACFAFVPPGLPNQTVVMLATLFTLLGAVCFFIGALMTLQESPESS
>NZ_CP036262.1|WP_145354239.1|6241609_6243007_-|glutamate-decarboxylase
MPLHDKNSIRDLVDDEIYASSDMSVSMPKYKFPLQEHSPRDVYSAVHDELMLDGNSRQNLATFCQTWAEPEVHKLMDECMDKNMVDKDEYPQTAEIEGRCVHMLADLWNSPDAANTIGCSTTGSSEAAMLGGMAMKRAWEAKRKAAGKSIDKPNLVTGPVQVCWHKFARYWDIELREVPMEGDRLILNAEEVVRRCDENTIGVVPTLGVTFTCQYEPVKEIADALDQLQESTGLDIRMHVDGASGGFLAPFCAPDLVWDFRIPRVKSINASGHKFGLAPLGVGWAIWREEADLPEEEIFWVNYLGGNMRDIALNFSRPGGQIVCQYYNFLRLGHEGYRKIHTACYETAKYIAGEVAKLGPFDVIYDGDMASGIPALCWKLKEGVDPGFSLYDFADRLRARGWQVPAYSLPPKREDLAIQRILVRHGVSRDLGSLLVEDMKRAIDYYKSHPVHTPMSADEASGFHH
>NZ_CP036262.1|WP_145354240.1|6243244_6244741_-|mannitol-dehydrogenase-family-protein
MSQSVSLNQNNLVRLSPEIARPEYQRTEGRAGIMHVGVGGFHRSHEAYYTDALMQIQETPEWGICGVGLREADRQMAAVLEKQDSLYTLITKHPAGDIENRVIGSLTGFMMGCDDPAAVIERMANPDIRIVSLTITEGGYNVDTETGDFDFSNPDAQHDLQNPTTPRLVFGYLTAALRLRRANGIPAFTVQSCDNIQHNGNLTRKMVLGFARRQDPELADWIENEVCFPNAMVDRITPVTTAEDIRYLDEKMGLLDEWPVTCEPFCQWVIEDRFSDGRPEWELVGAQFVPDVTPYETMKLRLLNAGHSVLGILGAIYGFGTIDEAVSDKLFAKFLRRFMDLEATPTLDAVEGIDLDAYKNTLIERFGNPNIKDSLARICLESSSKLPVFLLPTIQANLDRGGSVKYAALVIAAWCFYSDKGVDQHGRELEIVDELKQALHDAAKRTHDDPLSFLKLKSVFGDLAMNERFANTYADLVAQLSNDVDVSALMSEIIESDT
>NZ_CP036262.1|WP_145354241.1|6244927_6246646_-|hypothetical-protein
MSSDTSRQAIASMKQEQVPIPEHRLHGWTHFLGLYAGEHVAATEFVIGATFVALGATTKDILIGLLIGNVLAILSWTLITAPIAVQTRLSLYTYLDKIAGDSMTKLYNWANVLIFMVISAAMITVSSTAVRLLFDIPAQLQWYPTSAPFVAVVLSVGIIVVFVAMYGFNAVAEFSSICGPWLVVMFTSGALVLFPALAESVLGRTQLLAFADFIKIGDQSIWTGVNSSGEPGIGLLEVIGFAWAANTITHFGLIDMALLRYAKKSIYGLCTSAGMLFGHYVAWIAAGIMGAGTAVLLKSTIVELDPGDVAYRALGLSGYVIVIVAGWTTANANLYRAGLAAQAIFHNHSRGAVTLTVGCITVVIACFPFVFGQMLPLLTYAGLLVVPVGGIVFAEHVVFPRIGFTRYWAKYRKLDHSTPAVVSWAAGLVFGFGLNAMNVMSFYYLFLPTWLFTIVVYTLLAKRYGAAEKYPDEEQADRELTEAIQVFQKQQAHDEGEPVKDHLMASKVLKGVAWTSLTLTLVLALKVMFGSPNMSVYEANAAIFYTWGFVFTISYFVSAYWVLRRRKALNSH
>NZ_CP036262.1|WP_145354242.1|6247031_6248342_+|VCBS-repeat-containing-protein
MIVSSDFPAATVLGCLSIGIDPTPTIDRVLMFRLLVVSLFCAFMVIPQMGRCEDANDWKQFAGVQGPSGWRVNVIQPDPKNHGPDGFNHHDWDGDGDLDVFVNFEEGGYSRLYSNPGKVKIRQPWVDYVEFPPHGKCEDSGIGDLDDDGDIDYVANGGHVYFNPGKQKLKDSQNWVQMTLFENEARNPVVGDIDGDGLDDLIVGANAWYKQPANNKQDAAAWKRYELGEAKWSMSCILHDIDGDGDKDILVQERKKQGTFYYENPGVEKITDRWPVKIIDPEIGGMFMVLGDVNDDGRLDLVKAADKICIFLRTNNLGPPIYKKIEVDCPDQPAGVRVKAKPKGVAILELNNDRPHREIVIIPEYEAQLWYLSFTGDGMSPENWTSTLMDMPYPESRKKMDNAFLVDLDGDGDLDIATTEENGGWGIIWFENPANH
>NZ_CP036262.1|WP_145354243.1|6248803_6249388_+|hypothetical-protein
MNALSKLLCSAAMLTFTTTAFAQPPGGGRGGRGQGGPSPVERLMTLDVNGDGQLTVNEVTDARMKPMLNRADTNQDGAVTKAELTAMFGGQSADGRPGGPGGAGGGMRGGPGGGGPPEIGQIIPSFLQEQLGLSEEQQSALAKLQAEVDAQLALILTAEQQQQLKQGPGGPGGPGGQQGGGRERAGRGRPPADN
>NZ_CP036262.1|WP_145355813.1|6250383_6250623_+|hypothetical-protein
MAMQYQQQALMVQRQLAYQMYANAQQQRLAMMQREAKALPYRLARAEAKRAARAERIAARLREQDQTSDDYTLTSVSTD
>NZ_CP036262.1|WP_145355816.1|6251003_6252374_+|terpene-cyclase/mutase-family-protein
MMIHLVLLLALALISTSSGVVGRIELTLRQSSAPVTTELMDFSIAAMDLDNAPSEESSIEFQEEITPVEIEIPVNLTSLKFDLDSIAPRKLSPTPPPTGKASATNMFSGRTGRMKQQLLLEAGGNADTENAVAMGLEWLKRNQLKDGSWSLRGPYQGGARSENNVAATAMAMLAFMGAGSTHRGGEYEKELWKAVRWLVKKQDRQGFMASAAADHEKMYSQAQATIALCELYAMTGDSWIRPYAQLSCDFACRSQSTGGGWRYRPRFDSDTSVTGWFVMGLKSGEAGGLKIDPKVLKRVDGYLDSVSAGSKDDYYNVGYSYMIGDAPSPSMTAEGLLCRQYIGWDRNMRGMRNGLDTLVKNHPISMRSQDVYYWYYATQALHHFGGPLWTEWNDKLKVALPAAQQTRGPEKGSWAPNQDAWGTHAGRLYTTCLSLYCLEVYYRHMPIYAPEEINDA
>NZ_CP036262.1|WP_145354244.1|6252343_6252547_-|hypothetical-protein
MSRNVFFGDMETWRHGDMETWRHGDMETWRKRVRFLFSEVYFCLFLLKACVTNWGVGIHASLISSGA
>NZ_CP036262.1|WP_145354245.1|6252648_6254388_+|matrixin-family-metalloprotease
MLFFRSSKSCHHQPKKRRRLAAEPLEARRVLAASLGWDGPGLGSTELTYYIGNSPDSLSQAEATAAIETALAAWSSVADITFTPTSQAGLQDSIDISFTNIDGVGGTLAQAYFPDDINPARIAGDIQFDIADGWEVGNSLGNQAFDLVYVAVHEIGHSLGLDHTDTLSSVLAPYVSPSQSFSSLSAEDTESILNLYAAADGVTIPETPTEETPTEEIPDDQTATNDSDTDSSSDSDEDPFPRRRWNRSGNWHRWGGRLDAEAPEYNYVNPTDVNSDGITTALDALSIINQLNRSSAGVSEEGVDIERLCDTNGDGTITALDALTVINALNRNSLASANASEVYDTSDLDDDIDATVEATVEATEVADDNLATDDEPEETTEVSEDTDGLTNETDETDDNEDPIDDGGLVDETDSSDTDQEDCHEGEHLPLHIAHGGLLIQNAEMLITRFDTDDDAALSEAEVSERLWTRLNELDIDADGDGLVTASELETAATAARQEAFDGQDADGDGQLTESELSERFWEKISDADSDLDGGVSFDELDAFFVTQQDQFAETGGRSHHLRHQHLSDAVFALIGRRGR

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Crispr_ID: NZ_CP036262_21

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_21

6408394-6408549

Orphan

Consensus_repeat	Method
CCAGCAGGCACGAGTCTCGGAGAGACTCTGCTACGTGCCATGACGCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_21

>merge|NZ_CP036262|21|6408394-6408549|CRISPRCasFinder
CCAGCAGGCACGAGTCTCGGAGAGACTCTGCTACGTGCCATGACGCCGCGGCAGATGGCGATACCCGGGCAGCCACTCTCGTAGCTCCGCCTCTCCGAGGCGGAGAGCCCAGCAGGCACGAGTCTCGGAGAGACTCTGCTACGTGCCATGACGCCG

>NZ_CP036262|21|17|6408394-6408549|CRISPRCasFinder
CCAGCAGGCACGAGTCTCGGAGAGACTCTGCTACGTGCCATGACGCCG	CGGCAGATGGCGATACCCGGGCAGCCACTCTCGTAGCTCCGCCTCTCCGAGGCGGAGAGC
CCAGCAGGCACGAGTCTCGGAGAGACTCTGCTACGTGCCATGACGCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354337.1\|6401420_6401891_-\|DUF420-domain-containing-protein	unknown	unknown	gnl\|CDD\|377257
NZ_CP036262.1\|WP_145354346.1\|6413508_6420315_+\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225858
NZ_CP036262.1\|WP_145355840.1\|6403488_6404424_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP036262.1\|WP_145354336.1\|6399175_6401437_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036262.1\|WP_145354342.1\|6408653_6409316_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354347.1\|6420400_6423775_+\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|237108
NZ_CP036262.1\|WP_145354350.1\|6425511_6426366_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|372616
NZ_CP036262.1\|WP_145354338.1\|6401887_6402577_-\|redoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239266
NZ_CP036262.1\|WP_145354343.1\|6409843_6410608_-\|methylamine-utilization-protein	unknown	unknown	gnl\|CDD\|259883
NZ_CP036262.1\|WP_145354344.1\|6411008_6412337_+\|phosphoribosylamine--glycine-ligase	unknown	unknown	gnl\|CDD\|234856
NZ_CP036262.1\|WP_145355837.1\|6402576_6403410_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|130314
NZ_CP036262.1\|WP_145354335.1\|6397148_6398054_-\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP036262.1\|WP_145354341.1\|6406809_6408144_-\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|365823
NZ_CP036262.1\|WP_145355834.1\|6398007_6399036_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|285027
NZ_CP036262.1\|WP_145354351.1\|6426473_6427376_-\|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	unknown	unknown	gnl\|CDD\|236467
NZ_CP036262.1\|WP_145354345.1\|6412765_6413488_+\|4'-phosphopantetheinyl-transferase-superfamily-protein	unknown	unknown	gnl\|CDD\|225524
NZ_CP036262.1\|WP_145354348.1\|6423774_6424632_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|274428
NZ_CP036262.1\|WP_145354339.1\|6404542_6405544_-\|protoheme-IX-farnesyltransferase	unknown	unknown	gnl\|CDD\|260120
NZ_CP036262.1\|WP_145354340.1\|6405599_6406643_-\|cytochrome-oxidase-assembly-protein	unknown	unknown	gnl\|CDD\|224528
NZ_CP036262.1\|WP_145354349.1\|6424628_6425501_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|132144

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354337.1\|6401420_6401891_-\|DUF420-domain-containing-protein	gnl\|CDD\|377257	pfam04238, DUF420, Protein of unknown function (DUF420). Predicted membrane protein with four transmembrane helices.	1.99899e-40
NZ_CP036262.1\|WP_145354346.1\|6413508_6420315_+\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP036262.1\|WP_145355840.1\|6403488_6404424_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.59925e-87
NZ_CP036262.1\|WP_145354336.1\|6399175_6401437_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	1.43309e-06
NZ_CP036262.1\|WP_145354347.1\|6420400_6423775_+\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|237108	PRK12467, PRK12467, peptide synthase; Provisional.	0
NZ_CP036262.1\|WP_145354350.1\|6425511_6426366_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|372616	pfam13489, Methyltransf_23, Methyltransferase domain. This family appears to be a methyltransferase domain.	0.00114771
NZ_CP036262.1\|WP_145354338.1\|6401887_6402577_-\|redoxin-domain-containing-protein	gnl\|CDD\|239266	cd02968, SCO, SCO (an acronym for Synthesis of Cytochrome c Oxidase) family; composed of proteins similar to Sco1, a membrane-anchored protein possessing a soluble domain with a TRX fold. Members of this family are required for the proper assembly of cytochrome c oxidase (COX). They contain a metal binding motif, typically CXXXC, which is located in a flexible loop. COX, the terminal enzyme in the respiratory chain, is imbedded in the inner mitochondrial membrane of all eukaryotes and in the plasma membrane of some prokaryotes. It is composed of two subunits, COX I and COX II. It has been proposed that Sco1 specifically delivers copper to the CuA site, a dinuclear copper center, of the COX II subunit. Mutations in human Sco1 and Sco2 cause fatal infantile hepatoencephalomyopathy and cardioencephalomyopathy, respectively. Both disorders are associated with severe COX deficiency in affected tissues. More recently, it has been argued that the redox sensitivity of the copper binding properties of Sco1 implies that it participates in signaling events rather than functioning as a chaperone that transfers copper to COX II.	2.80154e-34
NZ_CP036262.1\|WP_145354343.1\|6409843_6410608_-\|methylamine-utilization-protein	gnl\|CDD\|259883	cd04221, MauL, Methylamine utilization protein MauL. MauL is one of the products from the methylamine utilization gene cluster in Methylobacterium extorquens AM1. Mutants generated by insertions in mauL were not able to grow on methylamine or any other primary amine as carbon sources. MauL belongs to the blue or type I copper protein family. They are involved in electron transfer reactions with the Cu center transitioning between the oxidized Cu(II) form and the reduced Cu(I) form.	7.97342e-21
NZ_CP036262.1\|WP_145354344.1\|6411008_6412337_+\|phosphoribosylamine--glycine-ligase	gnl\|CDD\|234856	PRK00885, PRK00885, phosphoribosylamine--glycine ligase; Provisional.	0
NZ_CP036262.1\|WP_145355837.1\|6402576_6403410_-\|ABC-transporter-permease-subunit	gnl\|CDD\|130314	TIGR01247, drrB, daunorubicin resistance ABC transporter membrane protein. This model describes daunorubicin resistance ABC transporter, membrane associated protein in bacteria and archaea. The protein associated with effux of the drug, daunorubicin. This transport system belong to the larger ATP-Binding Cassette (ABC) transporter superfamily. The characteristic feature of these transporter is the obligatory coupling of ATP hydrolysis to substrate translocation. The minimal configuration of bacterial ABC transport system: an ATPase or ATP binding subunit; An integral membrane protein; a hydrophilic polypetpide, which likely functions as substrate binding protein. In eukaryotes proteins of similar function include p-gyco proteins, multidrug resistance protein etc. [Transport and binding proteins, Other].	1.42494e-36
NZ_CP036262.1\|WP_145354335.1\|6397148_6398054_-\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	1.28237e-28
NZ_CP036262.1\|WP_145354341.1\|6406809_6408144_-\|c-type-cytochrome	gnl\|CDD\|365823	pfam00034, Cytochrom_C, Cytochrome c. The Pfam entry does not include all Prosite members. The cytochrome 556 and cytochrome c' families are not included. All these are now in a new clan together. The C-terminus of DUF989, pfam06181, has now been merged into this family.	4.61482e-11
NZ_CP036262.1\|WP_145355834.1\|6398007_6399036_-\|AAA-domain-containing-protein	gnl\|CDD\|285027	pfam07726, AAA_3, ATPase family associated with various cellular activities (AAA). This Pfam entry includes some of the AAA proteins not detected by the pfam00004 model.	5.43664e-88
NZ_CP036262.1\|WP_145354351.1\|6426473_6427376_-\|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	gnl\|CDD\|236467	PRK09328, PRK09328, N5-glutamine S-adenosyl-L-methionine-dependent methyltransferase; Provisional.	7.40735e-102
NZ_CP036262.1\|WP_145354345.1\|6412765_6413488_+\|4'-phosphopantetheinyl-transferase-superfamily-protein	gnl\|CDD\|225524	COG2977, EntD, Phosphopantetheinyl transferase component of siderophore synthetase [Secondary metabolites biosynthesis, transport, and catabolism].	1.26573e-33
NZ_CP036262.1\|WP_145354348.1\|6423774_6424632_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|274428	TIGR03101, hydr2_PEP, exosortase A system-associated hydrolase 2. This group of proteins are members of the alpha/beta hydrolase superfamily. These proteins are generally found in genomes containing the exosortase/PEP-CTERM protein expoert system, specifically the type 1 variant of this system described by the Genome Property GenProp0652. When found in this context they are invariably present in the vicinity of a second, relatively unrelated enzyme (ortholog 1, TIGR03100) of the same superfamily.	1.31427e-18
NZ_CP036262.1\|WP_145354339.1\|6404542_6405544_-\|protoheme-IX-farnesyltransferase	gnl\|CDD\|260120	cd13957, PT_UbiA_Cox10, Protoheme IX farnesyltransferase. Protoheme IX farnesyltransferase (also called heme O synthase, heme A:farnesyltransferase, cytochrome c oxidase subunit X [Cox10]) converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of the heme B porphyrin ring with a hydroxyethyl farnesyl side group. It is localized at the mitochondrial inner membrane. Eukaryotic Cox10 is important for the maturation of the heme A prosthetic group of cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, that catalyzes the electron transfer from reduced cytochrome c to oxygen. Prenyltransferases (PTs) catalyze the regioselective transfer of prenyl moieties onto a wide variety of substrates and play an important role in many biosynthetic pathways.	7.2017e-81
NZ_CP036262.1\|WP_145354340.1\|6405599_6406643_-\|cytochrome-oxidase-assembly-protein	gnl\|CDD\|224528	COG1612, CtaA, Uncharacterized protein required for cytochrome oxidase assembly [Posttranslational modification, protein turnover, chaperones].	2.98065e-16
NZ_CP036262.1\|WP_145354349.1\|6424628_6425501_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|132144	TIGR03100, hydr1_PEP, exosortase A system-associated hydrolase 1. This group of proteins are members of the alpha/beta hydrolase superfamily. These proteins are generally found in genomes containing the exosortase/PEP-CTERM protein expoert system, specifically the type 1 variant of this system described by the Genome Property GenProp0652. When found in this context they are invariably present in the vicinity of a second, relatively unrelated enzyme (ortholog 2, TIGR03101) of the same superfamily.	2.00201e-12

>NZ_CP036262.1|WP_145354341.1|6406809_6408144_-|c-type-cytochrome
MSGSLSNVCRSLVAVGWVGMAVAICLFVAPGCDSQPISFSGNALEKVKQEHVSGADLGQAESDIQAIMQAWFGTPDQPIVPVALQDLVQVDRIERSAGPVSSTEDGEHQGLYREHCAVCHGLNGNGRGPASGLQNPYPRDFRMGVYKFKSTPRGTPPTREDLLATLHRGAPGTAMPTFHSLPESDREALVDYVIYLSVRGMLERQLWQIAAEEFDYDSQPLPPEERLYAAGNEGTDDPAFVQQVAAIDELLLEITQAWLNAPQLALEIPEVPADVGRNVGTAEEEDSELVEIHDASVARGKALFHGQTANCVGCHGPAGKADVATLDFDDWTKDWTTRINITPTDTDAIAPFRAAGALRPRPAKPRNLQLGAFHGGSDPGLLYTRIVNGIDGTPMPAMELVEHPQPVGLTQRQVWDLINYVLSLSPADVAPLASESLVLPESSR
>NZ_CP036262.1|WP_145354340.1|6405599_6406643_-|cytochrome-oxidase-assembly-protein
MSDSAIQTQEDSYRPWLYRWTLLVLGLVWPLVWVGSLVTTQDAGMSVPDWPNTYGDNLFLYPLETWLSGPFDLFIEHGHRLLGALVGFVAIIVVAVAFWTERRRWVQGLAVLGLVLIIVQGILGGMRVVLGDRLLAMTHGCTAPIVFALFTVLAVVTSRWWSQIRSGPSEVDSPTKTEGSASGSDGARSSLKVVRGGWLASVVVIACYFQLVLGAMLRHVSMEATPGGFTHTVAMHVLLAFVIWGLTAILWLRLRGCGEKTLSRPGGALVGLVAVQIALGLTTWVVHYGFPMFQDYGFPARYLVQAKSFWGSFVICGHVATGSLILATAVLLTTRTFRIKHLRRTSS
>NZ_CP036262.1|WP_145354339.1|6404542_6405544_-|protoheme-IX-farnesyltransferase
MSLAAPSPPIRLHANADTSVVGVDSVLQRESSATRDEEAVAKAHPGLLRDLIVLTKPRIVIMVLVTTGVAAVVAAGWQLSPLVLLHALLGTAAVGASAGTMNQIWERRLDCGMKRTRSRPLPAGRITLFWAVVYCGVLGITGTAYLSWFSGPAPAFFGIATWLTYVLIYTPMKTRTSWNTTVGAVSGALPMMIGYTAAGGDVLGIRGWLLVAVLVAWQYPHFMAIAWMYRREYGEAGFLMTPVVEPTGRSAAAQSVVGAFALLAVLVALVWMTASGWSAVGLSLLMVAVSFGLVRDSIRFAYLKTDASARRMMFASLLQLPSAMIVLVIAALV
>NZ_CP036262.1|WP_145355840.1|6403488_6404424_-|ATP-binding-cassette-domain-containing-protein
MSPAVIQVAGVEHRYGDRAALQGVDLTVQQGSIFALLGPNGSGKTTLFRLISTLMPLQKGQITVAGAEVRDVIEVRKRIGIVFQSPSLDKKLSVDENIACQAALYGLSGAAFRKRRDEVLQALGLTDRRKEICEKLSGGLKRRVELAKGMLHRPRVLLLDEPSTGLDPGARLDLWEALRSMAAEGMTILLTTHLLEEAEKADQLAILAEGKIIANGTPDQLQAEMGDGLVTIHSEDPEATEKLVQEKLGLKVQRVQQQIRIHSDRPADLVPKLAELLGESARSITVGRPGLEDVFIAKTGHRFWSTSEAQE
>NZ_CP036262.1|WP_145355837.1|6402576_6403410_-|ABC-transporter-permease-subunit
MPTTVHSPSGWGAAWMLARREWVRFFRQRNRVTAAVVQPLLFWLLFGTGLRGSFEGAGGQDFIQFFLPGTVALIVLFTAIFATISVIEDRREGFMQAVLVAPVGRWPVLAGKVIGGGAIAWVQAVFFLTLVYAFGTAPLSFSIFPLMLLLAVLALSMCGLGMIVAWPMDSTQGFHAIMMLGLMPMWLMSGAFFPVPAAGEESLAMGQTVLRWVMLANPLTYGLAEMRHLLYPAVDFAEGGFAPDSVTNWIVSVLFMVAMLSIAWYLMRGSKKADLVA
>NZ_CP036262.1|WP_145354338.1|6401887_6402577_-|redoxin-domain-containing-protein
MRTAVHIFLIVVIGLVIGLALRQMRNQSQRQHTVTIKGPDGDIEVVIDEEQPTRVEAPPKPDLPEDANWVREFTLTERSGREVTSESLKGQPYVVSFFFTQCPSICIQQNQALKELADKFAGQDVKFLSISVDAENDTPEALREYAARFGADPDQWLFLTTDDPIYIQRVGAEMFQVSANLQHTERFILMNPEGDMEALYRWSDPRSLKRLEKDLQEMIAANKTAKDAA
>NZ_CP036262.1|WP_145354337.1|6401420_6401891_-|DUF420-domain-containing-protein
MMDWLAENLPHATASLNALATILLLLALWQVKRGNIKAHRNLMLTALSVSVLFLGLYLLHKFALLETTGSPNKKFPRDPAVASQGAFIVYLLVLLTHIPLAITVPVLAVWAAILGLKDRRSAHRRLVRWAFPIWLYVSISGVVVYLMLYQIYVPPQ
>NZ_CP036262.1|WP_145354336.1|6399175_6401437_-|PQQ-binding-like-beta-propeller-repeat-protein
MFRLSRVRSIQRFGVMTLVVCFWVGGNLSLFAQSQRLYEIEPAQRLSFNQLDQLIIAGEADAAVDLAVQMLDSTDGRLMRVPDSLRTDADLIAENYQPAELAVHDRLLRLGLKYPETLQLYRQRFDRVAKSEWERAVQVVEPEEARKALLEVSRRYFSTSYGDDVLLSLADLDLRAGRLQSAIDHLVRIDPFWQPRSPVPAGVSSPESAAVSATDWNTLLATLRRDPKTPLPFSVIDSLVQQVQNRKGLPLGCYRNSSIPLRQVGDRLIAAYRARGADILVVELERIVQVAADEVSGDQEADSLKVASAEPEWSAVVDGAPGEKHQRVLQGSARYLQNVDKNSLPPLAAGVNEKVSVRSFPAIVDGVAFIHSGSEVFARSLQTGQPWPSGIGTEAIHVATNTDTLLWPAGLPLSGMPRFDLVAGGRWLVGSFGSRYVGQQAYRSQRTASQLVVLDRYREGALQGGYPVRLPDDYVFASRPVLLGDRCFIAVRSTDGAAQSITLQCYDLPTGNILWASPPFVMQRLVKEQIAVETIPLVLAEDRLVIHAEGVTASVSVADGRLQWSVRHPLAELDSGGFPRQRPAAVKSDSALGVVGGEVIVAGVDMDRVVGLNAADGQLRWATAAGVGDDITHVIGQVAGQWVLGGQQLIWLKALSGDVLSSFPEGDVDQVGGGIDSPAGVGTGILVDGFVYWPTSESIYVFPGAVDENDRGTAIPRMVDRISLRPFGRRGGDLSESDGWILNSTPEAIVVLK
>NZ_CP036262.1|WP_145355834.1|6398007_6399036_-|AAA-domain-containing-protein
MTEQLHRRIVGQEEVIEQVLIALFSGGHCLLVGVPGLAKTLLVHSLSEVLQLQFSRIQFTPDLMPADITGTEVMQEDRASGERHFRFIEGPVFANIVLADEINRTPPKTQAALLEAMQEKQVTAAGQRHALPNPFFVLATQNPIEQEGTYPLPEAQLDRFMFDIRIRHMSEDDELAVVMRTTGDGQESIQPVLNADELVELIQTVRRVPVAASVARYATRLARLSRPADTSAADGGTKTLPVSQRVDQFVQWGAGPRGSQYLVLGAKAKAALDGRMMVEREDIRSIAKPVLRHRMRLNFAARAEGLSADALIDELLDAIDQQEKSDLHGSELEKVFRSADAR
>NZ_CP036262.1|WP_145354335.1|6397148_6398054_-|DUF58-domain-containing-protein
MDPNWKKFFDPQTLAELSGSGLRRLRPFDGGALTGVHRSSRHGHSVEFAEHRPYVLGDDLRSVDWKVYARTDRFFLQNREDETALVCHLMLDASGSMAFAGLQPSGDAQSKFDYAARVAASLGFITLTAQDQCSLTFLGGNGIDLPLSNGEPQVQGMVDVLARCQVEGDDHVGQQVQQALARLTRPGIVVLISDLLDSPQAIETAVRYVRAAGHDLFVIQVLHPEEKELSVHGMTRFQGMEGEPPVDLQPEAFAEAYHEAMQEFCQSIEQVCEQTETPFLALTTDQPIGSMLAARLNQYYG
>NZ_CP036262.1|WP_145354342.1|6408653_6409316_-|hypothetical-protein
MDQSDLSFFDPAADWDVVERHLPHWGQPGCMCFVTWRLGDALPAEILVQLDVAIGDLLRGAGLDPDSDLRVQLSQHPCKFRSDVYHKLFQLRDRFLDSGYGACHLANRECAEIVLESLLKFDGERYFMTDVVVMPNHAHFLVGFASQTRFLKQCTEWKRFSGRAVNRYLGIQGSFWQVDQFDHLLRGEKWFDYYRQYIVDNPKKASLRLGEFLHFQKRLA
>NZ_CP036262.1|WP_145354343.1|6409843_6410608_-|methylamine-utilization-protein
MRRFLLSAALLCFASQLNAGDLKIQFLFDGVVPPPTAINVNRDEAFCGKHGLVDERLVVNPTSKGIKNVVVYVYTGRGGSKLPDQTPKNATHVLANKNCRFEPHIVIAQVGDTLKVTNPDPVGHNASMNFLKNTPQNPMIPSGQEVEVELKESEPAPIPVTCSIHPWMQSRLVVLDHPFAAVSDEDGVLVIKDLPNEELNFRVYVEAADGALDEVDLNGKTVKWKRNRFDVDIKDGMNDMGVVKIKANQIKYGD
>NZ_CP036262.1|WP_145354344.1|6411008_6412337_+|phosphoribosylamine--glycine-ligase
MPAESADNSSIPATKKVLIVGNGGREHALAWKLAQSPQVAQVFVAPGNAGTAIDATNVSIEASDKPGIIKFAIENEIAFVVVGPEAPLVDGLVDDLQAAGIRAFGPSAAAAELEGSKVFCKNLLRASNIPTAEYQTFRTASDASRFIKDRYPDSEQDVPVVVKADGLAAGKGVIVCSTRSQALDAINRIAGVREFGEAGDVLIIEERLMGQEASVLAITDGSTIITLPAAQDHKPAYDGDLGPNTGGMGAFCPTPLIDAEMMARIERDILVPVVHAMKRSRRPFRGILYAGLMLTAAGPKVLEFNVRFGDPECQPLLMRMKGDLCEIIEAVIDGRLADVDPPEWDERPSICVVMASEGYPSAYEKGRVIKGLDKAAEMSDVKVFHAGTQNIGTTVINNGGRVLGVTAIGNSISDAKLKAYKAVKEIRWPGAWCRKDISDKAL
>NZ_CP036262.1|WP_145354345.1|6412765_6413488_+|4'-phosphopantetheinyl-transferase-superfamily-protein
MSVCKTVASRPPFVTMASVASVRPRHDASARTLGETLSAKIHPWMPKDIAWQLSPLQPADSAYPNRLTKRQREFAAGRSVASELLKTFGVSERVGVNADRSPAWPKGFAGSITHSDHWVWCTVAHRSGYLSVGIDTEPIVDESTAQQLHEQIATETEWQIATIPSLDQCQRFTLVFSAKEAFYKCWYPMMGTVLHPKQIEVCQLDENRITMKRNSDPFQLAIRYLIYGDNVFTATWWREN
>NZ_CP036262.1|WP_145354346.1|6413508_6420315_+|amino-acid-adenylation-domain-containing-protein
MNIQERYSLLNNTKAATPQLHLHQWIEQQSQANAEKTAVVCEQDSQSYASLSAWSNQIAGWLQTKGVGIGDRVGICCRRDVDLPATLVGILKSGASYVPLDPEYPVDRLKFMVKDADVKHVLGHQSHGDLIDQFDVDATMIDQQRDAIESADVYTEVHTDPRTDVAYVIYTSGSTGNPKGVLVPHLAVVNMLHSMISTPGFTADDRILATTTLSFDISVAEMFLPLVTGGSVAVVDRQTARDSERLVQAIQKHHVTFMQATPAMWRMMVEAEFSGTSQMKFVTAGEPLPRDLIDPLLERCGELWNLYGPTETTVYSTASRILNSTDRILIGKPIDNTHSYIVDDSDQLCDVETPGELLIGGLGVTMGYLNRDALNAEKFVTWNGESVFRTGDLAQITDDGQIDHLGRIDSQIKLNGHRIELGEIDAAMATDASVRIAATVLREDTPGDVRLVGYVLPADNQTPDVVALREELSKSLPDYMVPSSITVVDSFPYTPSGKLDRGAFPMPATKRPDIETPYIAPKSEQEKQLATIWSNVLQIDRIGTHDSFFDLGGNSIRATKVVSAARNQMGINVSIAEFFDRPTIDAFLASSAKSEEQKTLPTPAASRSRTNASGRFAIVGMAARMPGAEDVNTFWQNLINERESITFFDTDELDPSLDPRDTHSEHYVPARGILKDSDHFDARFFGMPPRTAEWTDPQQRVLLELAWTALEDAGMGNHSATATDDVIGIWAGTYATSYFIKNVLSNPERVREIGEFNAGLNNEKDYLATRIAHSLNLTGPAVSVSTACSTSLVALIEACKAIEGGLCDAAIAGGVSISHPQNSGHLHQTGSIFTPDGHCRPFDAFGAGTLFSDGAGLVVVKRLEDAIENNDRIYAVIRGFGINNDGSEKSSFGAPSIHGQSRAIAMAHASADVQAESIGYIEAHGTATPIGDPIEVTALREVFEAQTEQKQFCAIGSVKSNIGHTVAAAGVAGLIKTALSLHHECIPATLHFENPNPQIDFEDSPFFVCDRTIQWPRSSEPRRAGVSAFGVGGTNAHVILEEAPAVHAGETQERSGTLPVHLLPVSAKTETALSKSAKRLATYLESDRGSSIELADVAHTLANGRARMNWRAFVVAGDPQDASKAFSLQKAPRYQQQKWDGVERDVVFMFPGQGAQYLRMGHDLYQHCDVFRASLDRCCDLLTPSIDRDLRDILFPASDQHESATALLRETQFTQPALFAVGYSLAQTWMNWGIRPTAMMGHSIGEFAAACVAGVFSLEDAVRLIAKRGEMMQRLPGGSMLSVRLPGHTVEPMLSGDLAIASYNGPSLCVVAGPDDQVQTLQKELESNEVVCRSLQTSHAFHSPMMQEIVRPYAEFVRTVTLAPPSIPILSTVSADWMTDEQATDPNYWAAHLREPVQFSGAVTQMWKEDSSRILLELGPRRTLATLAKQHADDPKKQIALPSLSDNADDHTESKAMLSALGRMWLEGVSIDWKNVQTKGRTVSLPTYPFERKRYFMEPNQAKYRSLHPIPPSPVPADVLANLPSTETAPSIPTSLSSPSPCSAPNLPMNRKPAIITAIKDVFENSSGFDLNDFENDTTFFEMGLDSLGLTQTATALHKAFGIEVTFRQLLEETPHVDGLSNFLDEHLPRDQFREQAEPQQDHAANVASFTTNPIAADQSDLTGQITLDNNTASVTQSPVNVQTDQLGQVATGDMTYSIVQQQLQIMAAQMQWLAGTPVSVPATTTPLASSTSPQPQSRSPKEPSKDLTPPPFTNDAPPKAFGAAARVAKTDSALDASQQTALDEIIRLHNQMTPKSKAQAQQHRAYLADPRTVSGFRPNLKEMTYPLVVDRSKGVYLWDIDGNEYVDFTCGFGSNLLGHSHEITVNAINEQVQKDFSIGPQSPLAGEVAALFCELTGNQRMAFANTGSEAVLACTRLARSATGRDRIVMFNEDYHGILDEVLVRGSKSHKSFPAAPGIPKEHVSNTLVLDYGTDESLRIIQENIDTIAAILVEPVQSRHPELQPREFLHKLRALTEHAPTALIFDEVISGLRIGKGGAQEYFGIRADLASYGKVVGGGMPIGVVAGKAEYMDGLDGGFWQYGDDSRPEAGMTYFAGTFVRHPLTLAASKAILQHIKSEGQPMYDRLNQLGDYLTTELNKVATELNAPLFAANFGSLFKLQFHDEPLYSELLFAAMRRRGMHIWDHRPCLLTLAHTKSHVDQLVQALHESIIECQRHGFLTGDGYRKSSVSSAADQPPVSGAKLGKDKNNHPGWFIPDAANPGQFLQV
>NZ_CP036262.1|WP_145354347.1|6420400_6423775_+|amino-acid-adenylation-domain-containing-protein
MTPVLSNLNSVAATVAFVPGTQPENRYATSQAQLEVWLSAKQSEQANCAYNEISTLELRGPLDVDRLKQAIVKVCERHGSLRSTVGIDGQHILVHPRPQHAFSFVDWSIDPSKDIAAARRMVVQNEATTPFDLVDGPLLRAVLQKATDTQHWLTLTAHHLVMDGWSLALFYRDLGYFYDTLSGIQRDALAPASQYDEYALQMDQYMASDAGQADEAFWTKCYQGDIPVLELPIEKPRPSLRTFTAERMETTLPATLVAAVQKVGAKSGCSRYNTLLAAFTAYVAQISGCDDFGIGIPTAGQAALDHPELIGHCVNTMPLRTQVDSDTSFLSHMKQTRSRLLDAFEHQRYSYGTLLRKLAPARDPSRPPMLNVSFNIDPVMDTAQLGFTGFDLDITIEPRRFENFEWFINGVIRKDQSIELQVQYNSDLYTERAMECYFDGFRTFLEGVAASPDTRINDLPKVSLRMRQQAIVDWNATALDYPIEATLHSEFSRQATATPDAVCVRFGDQTLTYADVDSQSNRIARYLKSEGVQEGDLVGICVNRSEQMLVNLIAILKAGCGYVPLDPAYPSDRLQYMCDHSQLTTIVTERSLVPRITSFNKPHLAIDDAREAIANLDDSDVQTSANPNDTCYVIYTSGSTGKPKGVQVQHGAVVNFLYAMREAPGFTQDDSILAVTTLSFDIAVLELYLPIVFGGSVVIADTDTSSNGSKLADALEKHDITWLQATPATWRLLIQSGWQGKTKRNGQAFKVQAFKVLCGGEPMPNDLVDPLLKRCDQLWNMYGPTETTVWSAVYRITDASSPILIGKPIGNTQIYLLDQQGHEVSPGCEGEVYIGGAGVTQGYLHRPDLTEERFVDNRYRNPFVAYNNNKLYRTGDLARYTFDGNLQFLRRNDKQVKVRGYRIELGEIESHLKSHPAVAQCVVIVREDSPGDAKLVAYVIPKPEQSASAIELREHLRMSVPNYMVPQNFVTLDSMPQTNNGKIDYASLPSPKQNTASDDLLNATAEKPETEAEKRLAAIWQEVLETDQIGRDDNFFDIGGHSLLVMKVIAIVAETTSISLSPQDFLTGTLRHMAYQLEDVTGAADTTADASVKVGMETVDPAKPSSSAEPKHRLLRSLKGFWNE
>NZ_CP036262.1|WP_145354348.1|6423774_6424632_+|alpha/beta-fold-hydrolase
MEPRFIGDPHSQLLSIHHRAQGVHGNSKRAVVICPPIGQEYVQTHWSLRLFANQLARKGVHVLRLDYYGIGDSAGEIEDVTSTAVWLQNIATAIQHLQDNTGVETVTLVGLRLGATLAAQVADDNPNVNAVVLWEPVADGREYLDALRSNHHEMLDLWVRPIQTPNDESREEILGTRYSRELVREIEQTTLDPSSIVQPQLIVQLESDTRSFSHPTDGIQRVFRVADSDDWSDLRRLEVAWLRPTTIRMIVDSVDDMFDRLDRFEALSLPDSGMQLQELTAGVQQ
>NZ_CP036262.1|WP_145354349.1|6424628_6425501_+|alpha/beta-fold-hydrolase
MKETICRFGPNDSLLGILTRPDEDELIKDAPVALILNAGIVHRVGQFRLHVSMARQLAKQGYSTLRIDLSGLGDSAPRTDRSDSDNRAERDVRDAMDHLEQTIGAESFVLIGLCSGAYNAHKVSIKEDRVTGAVFLDGLVFQTSGYVRRHKIGRLFRYRFWRNAIKRRLSGKMPDHSESDANQLAASEFFDTGMSRESVRNDLQTLLDRNVQMLFIYTEGYDDICGRAQFYEMYGFRPSDQQQVEYYANAEHTYPIVENREIACVRIATWFADRFPRVAENRRILQNSSL
>NZ_CP036262.1|WP_145354350.1|6425511_6426366_+|methyltransferase-domain-containing-protein
MSSLLSIETASEASLKKRTAECIGRIVSTLSPGRTKMLYETPQSTPSGFVDKAIMAFLKRNAIQNHQEGFFERLHKDFWQGKGGEVFSSNCDNRFNDLFLTRQKDDITALKKTCLETKPKHLVEFGCSGGAVLNYLTQSIEGIDSATGIEINQEQVRRNQTSDEFDSRIDFVCDDGGDWLLANGQPQSLFVSNGGVLEYFRRERLDQMLTHISQQLGPATFFAIEPVACDHDFDQTNASIPFGNELSFSHNYPNLFQSNGFDVVHRSVVEFESWKMLAIIAVTR
>NZ_CP036262.1|WP_145354351.1|6426473_6427376_-|peptide-chain-release-factor-N(5)-glutamine-methyltransferase
MSTEQTEKTEPWTVLRLLTWTTDFFKKKGSDTARLDAEVLLADARGCSRIELYTAFNTELEQEPLVAFRELVRRRGEGTPVAYLVGYKEFYSLKFQVNPSVLIPRPETEHLVIEALDRAKSIAGEGKLHIADVGTGSGAIAIAIAKNLPRARVAAIDKSEQALQVARENVERYELQDRIVLQHGDLLQTIKMDASLDMVCSNPPYISQAEYDALDPGVREQEPEMALLCGPKGTETIEALIPQAARCLKPGGFLIIELSPMIADACADILKANEAFAADTVHLIRDLAGHKRILSAQKAA

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Crispr_ID: NZ_CP036262_22

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036262_22

6792199-6792286

Orphan

Consensus_repeat	Method
CGTAGCCGCGTCTCTCCGAGACG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036262_22

>merge|NZ_CP036262|22|6792199-6792286|CRISPRCasFinder
CGTAGCCGCGTCTCTCCGAGACGCGGAATTCCCGCCGTCTTGGAAAGAGGGAGCTACGGGCAAAGCGTAGCCGCGTCTCTCCGAGACG

>NZ_CP036262|22|18|6792199-6792286|CRISPRCasFinder
CGTAGCCGCGTCTCTCCGAGACG	CGGAATTCCCGCCGTCTTGGAAAGAGGGAGCTACGGGCAAAG
CGTAGCCGCGTCTCTCCGAGACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036262.1\|WP_145354579.1\|6794510_6795101_+\|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl\|CDD\|179314
NZ_CP036262.1\|WP_145354585.1\|6804313_6806506_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227713
NZ_CP036262.1\|WP_145354575.1\|6787836_6788640_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP036262.1\|WP_145354583.1\|6801384_6802296_+\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP036262.1\|WP_145354574.1\|6786310_6787597_+\|serine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235461
NZ_CP036262.1\|WP_145354581.1\|6798205_6799909_+\|solute:sodium-symporter-family-transporter	unknown	unknown	gnl\|CDD\|236699
NZ_CP036262.1\|WP_145354577.1\|6790738_6792181_+\|leucyl-aminopeptidase	unknown	unknown	gnl\|CDD\|234863
NZ_CP036262.1\|WP_145354576.1\|6788721_6790566_-\|UbiD-family-decarboxylase	unknown	unknown	gnl\|CDD\|376697
NZ_CP036262.1\|WP_145354570.1\|6781129_6782203_+\|SidA/IucD/PvdA-family-monooxygenase	unknown	unknown	gnl\|CDD\|188533
NZ_CP036262.1\|WP_145354582.1\|6800344_6801385_+\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|285027
NZ_CP036262.1\|WP_145354569.1\|6779609_6781133_+\|uroporphyrinogen-III-C-methyltransferase	unknown	unknown	gnl\|CDD\|381169
NZ_CP036262.1\|WP_145354580.1\|6796897_6797737_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036262.1\|WP_145354578.1\|6793020_6794457_+\|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl\|CDD\|235490
NZ_CP036262.1\|WP_145354568.1\|6779015_6779294_-\|30S-ribosomal-protein-S20	unknown	unknown	gnl\|CDD\|376586
NZ_CP036262.1\|WP_145354571.1\|6782786_6784091_-\|tRNA-(N(6)-L-threonylcarbamoyladenosine(37)-C(2))--methylthiotransferase-MtaB	unknown	unknown	gnl\|CDD\|223694
NZ_CP036262.1\|WP_145354586.1\|6806527_6809830_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376899
NZ_CP036262.1\|WP_145354572.1\|6784117_6784471_-\|ATP-dependent-Clp-protease-adaptor-ClpS	unknown	unknown	gnl\|CDD\|376861
NZ_CP036262.1\|WP_145354573.1\|6784678_6786094_+\|dipeptidase	unknown	unknown	gnl\|CDD\|349929
NZ_CP036262.1\|WP_145354584.1\|6802292_6804317_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131281
NZ_CP036262.1\|WP_145355904.1\|6795939_6796500_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036262.1\|WP_145354579.1\|6794510_6795101_+\|3-isopropylmalate-dehydratase-small-subunit	gnl\|CDD\|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	2.81034e-124
NZ_CP036262.1\|WP_145354585.1\|6804313_6806506_+\|hypothetical-protein	gnl\|CDD\|227713	COG5426, COG5426, Uncharacterized membrane protein [Function unknown].	0.000210342
NZ_CP036262.1\|WP_145354575.1\|6787836_6788640_-\|SDR-family-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	3.40928e-60
NZ_CP036262.1\|WP_145354583.1\|6801384_6802296_+\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	1.25216e-34
NZ_CP036262.1\|WP_145354574.1\|6786310_6787597_+\|serine--tRNA-ligase	gnl\|CDD\|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP036262.1\|WP_145354581.1\|6798205_6799909_+\|solute:sodium-symporter-family-transporter	gnl\|CDD\|236699	PRK10484, PRK10484, putative transporter; Provisional.	0
NZ_CP036262.1\|WP_145354577.1\|6790738_6792181_+\|leucyl-aminopeptidase	gnl\|CDD\|234863	PRK00913, PRK00913, multifunctional aminopeptidase A; Provisional.	0
NZ_CP036262.1\|WP_145354576.1\|6788721_6790566_-\|UbiD-family-decarboxylase	gnl\|CDD\|376697	pfam01977, UbiD, 3-octaprenyl-4-hydroxybenzoate carboxy-lyase. This family has been characterized as 3-octaprenyl-4- hydroxybenzoate carboxy-lyase enzymes. This enzyme catalyzes the third reaction in ubiquinone biosynthesis. For optimal activity the carboxy-lase was shown to require Mn2+.	7.84724e-133
NZ_CP036262.1\|WP_145354570.1\|6781129_6782203_+\|SidA/IucD/PvdA-family-monooxygenase	gnl\|CDD\|188533	TIGR04018, thioredoxin_reductase, putative bacillithiol system oxidoreductase, YpdA family. Members of this protein family, including YpdA from Bacillus subtilis, are apparent oxidoreductases present only in species with an active bacillithiol system. They have been suggested actually to be thiol disulfide oxidoreductases (TDOR), although the evidence is incomplete. [Unknown function, Enzymes of unknown specificity].	1.10877e-103
NZ_CP036262.1\|WP_145354582.1\|6800344_6801385_+\|AAA-domain-containing-protein	gnl\|CDD\|285027	pfam07726, AAA_3, ATPase family associated with various cellular activities (AAA). This Pfam entry includes some of the AAA proteins not detected by the pfam00004 model.	4.2774e-85
NZ_CP036262.1\|WP_145354569.1\|6779609_6781133_+\|uroporphyrinogen-III-C-methyltransferase	gnl\|CDD\|381169	cd11642, SUMT, Uroporphyrin-III C-methyltransferase (also known as S-Adenosyl-L-methionine:uroporphyrinogen III methyltransferase, SUMT). SUMT is an enzyme of the cobalamin and siroheme biosynthetic pathway. It catalyzes the first of three steps leading to the formation of siroheme from uroporphyrinogen III; it transfers two methyl groups from S-adenosyl-L-methionine to the C-2 and C-7 atoms of uroporphyrinogen III to yield precorrin-2 via the intermediate formation of precorrin-1. Precorrin-2 is also a precursor for the biosynthesis of vitamin B12, coenzyme F430, siroheme and heme d1. This family includes proteins in which the SUMT domain is fused to other functional domains, such as to a uroporphyrinogen-III synthase domain to form bifunctional uroporphyrinogen-III methylase/uroporphyrinogen-III synthase, or to a dual function dehydrogenase-chelatase domain, as in the case of the multifunctional S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase/dehydrogenase/ferrochelatase CysG, which catalyzes all three steps that transform uroporphyrinogen III into siroheme.	1.68021e-103
NZ_CP036262.1\|WP_145354584.1\|6802292_6804317_+\|hypothetical-protein	gnl\|CDD\|131281	TIGR02226, hypothetical_protein-transmembrane_prediction, N-terminal double-transmembrane domain. This model represents a prokaryotic N-terminal region of about 80 amino acids. The predicted membrane topology by TMHMM puts the N-terminus outside and spans the membrane twice, with a cytosolic region of about 25 amino acids between the two transmembrane regions. Member proteins tend to be between 600 and 1000 amino acids in length. [Hypothetical proteins, Domain].	5.54804e-25
NZ_CP036262.1\|WP_145354578.1\|6793020_6794457_+\|3-isopropylmalate-dehydratase-large-subunit	gnl\|CDD\|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_CP036262.1\|WP_145354568.1\|6779015_6779294_-\|30S-ribosomal-protein-S20	gnl\|CDD\|376586	pfam01649, Ribosomal_S20p, Ribosomal protein S20. Bacterial ribosomal protein S20 interacts with 16S rRNA.	2.41355e-20
NZ_CP036262.1\|WP_145354571.1\|6782786_6784091_-\|tRNA-(N(6)-L-threonylcarbamoyladenosine(37)-C(2))--methylthiotransferase-MtaB	gnl\|CDD\|223694	COG0621, MiaB, 2-methylthioadenine synthetase [Translation, ribosomal structure and biogenesis].	5.44455e-137
NZ_CP036262.1\|WP_145354586.1\|6806527_6809830_+\|hypothetical-protein	gnl\|CDD\|376899	pfam02687, FtsX, FtsX-like permease family. This is a family of predicted permeases and hypothetical transmembrane proteins. Buchnera aphidicola LolC has been shown to transport lipids targeted to the outer membrane across the inner membrane. Both LolC and Streptococcus cristatus TptD have been shown to require ATP. This region contains three transmembrane helices.	0.00353402
NZ_CP036262.1\|WP_145354572.1\|6784117_6784471_-\|ATP-dependent-Clp-protease-adaptor-ClpS	gnl\|CDD\|376861	pfam02617, ClpS, ATP-dependent Clp protease adaptor protein ClpS. In the bacterial cytosol, ATP-dependent protein degradation is performed by several different chaperone-protease pairs, including ClpAP. ClpS directly influences the ClpAP machine by binding to the N-terminal domain of the chaperone ClpA. The degradation of ClpAP substrates, both SsrA-tagged proteins and ClpA itself, is specifically inhibited by ClpS. ClpS modifies ClpA substrate specificity, potentially redirecting degradation by ClpAP toward aggregated proteins.	2.01825e-16
NZ_CP036262.1\|WP_145354573.1\|6784678_6786094_+\|dipeptidase	gnl\|CDD\|349929	cd05680, M20_dipept_like, uncharacterized M20 dipeptidase. Peptidase M20 family, unknown dipeptidase-like subfamily (inferred by homology to be dipeptidases). M20 dipeptidases include a large variety of bacterial enzymes including cytosolic nonspecific dipeptidase (CNDP), Xaa-methyl-His dipeptidase (anserinase),and canosinase. These dipeptidases have been shown to act on a wide range of dipeptides, but not larger peptides. For example, anserinase mainly catalyzes the hydrolysis of N-alpha-acetylhistidine while carnosinase degrades beta-alanyl-L-histidine.	0

>NZ_CP036262.1|WP_145354577.1|6790738_6792181_+|leucyl-aminopeptidase
MEFKTSPNVLPSDCIVLGIDADGQLSKSAQTIDQQAGNVLSRAVKAGDISSKSGKTTLVPLPETSDHAAALVIATGKTEELSVEQAYRLGAISLKTLSDRQRDQIGVTLTAGWAPEFVEAFVAGACAGSNGQGIYLAEPKLMAPKTVTLVGADEAAVRSGQILGNSVNLTRRLVNEPGNVIYPETFAQRAKTVADECGLAIEIWDEKKLEEENCQAILAVGRGSVHPPRLVKITYNGAPDNKDAPVALVGKGVTFDSGGLSLKPSPSMLDMKMDMAGAATVLGVLQCIAQLKLPCNVVGYMGLAENMLDGDNYRLGDVIRSRSGKTIEIHNTDAEGRVVLADVLDVANEGNPASIVDLATLTGACLVALGTKIVGLMGNNDALQSEIQTAAKEVGEHVWPLPMHSFFDEQVRSKVADLKNVGDGRWGGSITAAKFLEAFVGDTPWLHMDIAGPAFADSATPEQDAGGTGAMVRTLVQWLR
>NZ_CP036262.1|WP_145354576.1|6788721_6790566_-|UbiD-family-decarboxylase
MKHRSTRDAVEDLRRGGYLIECSDSVDPNLEIAEIQRRVYASGGPAVLFTNVKGCRFPMVSNLFGSLEQARYLFRDTLESVRRLIELKIDPPALARRPWRYAGSPLTAIRMLPRYRRSGPVKANQCQLSELPQLKCWPDDGGAFVTLPQVLSADPVSPDVLMKCNLGMYRVQLSGNEYDPQHEVGLHYQIQRGIGVHHQHAAAKNQALPVSINVGGTPAMTLAAVMPLPEGLGELTFAGALSGRRVGMLRDGKSAPFYADADFSIVGEIDPQATKPEGPFGDHLGYYSLQHPFPVMKVRSVYHRKDAIWPFTVVGRPPQEDTTFGQLIHELTGPIIPTVLPGVKGVHAVDAAGVHPLLMAVGSERYMPFSRAAEPQELLIQANAILGNGQLSLAKYLMIVNEADDPELDVDDCGAVLQHLLQRIDWRRDLHFQTRTTIDTLDYSGDGLNRGSKVILAATGPVRRELPTEVPSGLVLPDGFSNPQVVAPGVLAIEGPRCVAGDRLYRDAMVGFVASQTVGGPLDAFPWVTVCDDSRFAAAGLKNWLWVTFTRSNPAVDIYGVAEGIRDKHWGCRGALVVDARTKTHHAPPLMEDPDTTRQVDARATRGDALAKYL
>NZ_CP036262.1|WP_145354575.1|6787836_6788640_-|SDR-family-oxidoreductase
MSRIAKLFADPHPVALVTGSGAPRVGNVIARHLASLGCRIVIHANSSMEAAERTASELRSEGVETIVVQASIEKSEQVERMIEEVVETFGRLDILVNSAAIWEPKRLEDVTPEDVRRYFEVNTLGTFVAARSAGLQMVTQPKGGVIINIGDWGLVRPYLDHAAYFPSKGAIEGMTRSLAVELAERNRAVRVNCIHPGPVLLGDDLPTATQAAVMGSTLLKRVGTPEHVAHAVQFLVENDFVTGAAIPVDGGRTIYADDGLQTKHKIG
>NZ_CP036262.1|WP_145354574.1|6786310_6787597_+|serine--tRNA-ligase
MLDRKYILENADAVTANCTRRGVKCDVPKLVQLETERLEKLKEAQELNRQANEVSKQIGKAKDNDERQQFIDRGRELREAKDTAQKQTDALEEQILEIQRAIPNLTHPDAPTGGEEDATEQGFGKTPKPTFDFKPLDHLELAERHDMLDFEAGARVAGAGFYFLKNDAVRLDLALQQFAVAFLSDRGFTPVSTPDVALTEILKGTGFQPRGPETQIYSIENTELNLVATAEITLGGMLSGQTMQADELPLKLCGLSHCFRTEAGAAGRASKGLYRVHQFSKVEMFAFTSPEASDQMHEELRQIECELYDALEIPFRIIDTASGDLGGPAYRKYDLEAWMPGRGENGEWGEITSTSNCTDYQSRRLNIRFKTAGQKGTQFAHTLNGTAVATGRTMIAIIENNQQADGSIKVPTALQPWVGKAVIGEAVT
>NZ_CP036262.1|WP_145354573.1|6784678_6786094_+|dipeptidase
MPHFSLNRQTHVTSNTIDTLLDSHQQAHTEDLIEWLRIPSVSSDPKAKKEVREAGQWVADLLRNAGLQTEWIETQGHPLVYATTPPVPGAPVALVYGHYDVQPPEPLDLWDSPAFEPDIRDGNIYARGATDDKGQVLTHVQAVLRLLETGQPLPLQIKFLIEGEEEVGSENLERMLPELADKLACDVVVISDSSQFAPGQPAITYGLRGITTFELKVFGPSQDLHSGSFGGAVMNPGIALSKLIASMINDDGQIQLPGFYDDVQPLTDEERQQFASLPFEDAEFARSLGVAKLAGEKGYTTLERKWARPTFDVNGLTCGHQGPGAKTIIPATASAKLSFRLVPNQDPQKIAEALEAHVAQHTPVGVTTKITPDHGAPGMVANLKSPFIAAAQTALEAAFGKPPVLIREGGSIPIVQKFQETLGADCLLLGWGLNDDNAHSPNEKFCLADYHRGIKASAHLWQQIGSLNQNR
>NZ_CP036262.1|WP_145354572.1|6784117_6784471_-|ATP-dependent-Clp-protease-adaptor-ClpS
MKESQAAVLEPPAEREQQSRRQRTAPKRQPRYNVILWDDTDHSYDYVIMMLRELFGHPRERGMQMAKEVDSSGRVICMTTTMELAELKRDQIHAYGADGGVTRCKGSMSASIEPVPE
>NZ_CP036262.1|WP_145354571.1|6782786_6784091_-|tRNA-(N(6)-L-threonylcarbamoyladenosine(37)-C(2))--methylthiotransferase-MtaB
MSAKMRTVTLGCKVNQYETELVRQGLSRIGFDDAEGDEQADVCIVNTCTVTSEGDSKSRQMIRRLARRNPDSRIVVMGCYATRAPEEVASLPNVVDVVTDKRELPDLMTRFGVVDVPTGLDGFSGRQRAYVKVQDGCLLRCSYCIIPMVRPELTSRPKQHIVEEVQRLVQAGHHEVVLTGIHLGHYGVDWNRDKPKEEWVRLAHLVRELAELPGNFRIRLSSIEATEVTRELIEVMTDYPERIAPHMHVCLQSGSDSVLRRMRRRWGTRMFLDRCQMLQDALDQPALTTDVIVGFPGETDEEFEQTLETCRKARFSKVHVFPYSQRRGTPAAEMEDQVDKEVQAERVQRLLALEADLRQDYFKSLHGRTVQAIVESTRGLTGIGQVEDNEWVMRGTSCRFAPVEFFASQPVQRGTLVNLKVVDATSEKLVGLPV
>NZ_CP036262.1|WP_145354570.1|6781129_6782203_+|SidA/IucD/PvdA-family-monooxygenase
MNHAPLPSSEKAPRVLIVGAGPIGLELAVDLQRNRIPFEIVDAGPIGQTMNWWAPETRWFSSNERISIAGVPLLTKDQSKATREDYLNYLRGIAIQFNLRVRTYEPVTKIRRSEQGFDVDTMPQQSLRSDHYDKIVLAIGGTDRPRRLNVPGEDLPHVDGYLREPHRYFGRRVLIVGGRNSAAEAALRLHHAGAQVSLSYRGPALPEEGIKYWLLPELKGLCSAGRITAHFGSEVVRITPQETELRSAQSNETFSVKADDVLTLIGYEQNKSLFQSAGVNLQESTQHPEFDLATMETNVPGIYVAGTAVAGTQNSRYKTFLENCHQHVDKIVAHLTGQTATAQDDQFQKQITAQPES
>NZ_CP036262.1|WP_145354569.1|6779609_6781133_+|uroporphyrinogen-III-C-methyltransferase
MQLKCAQVYLIGSGPGDPGLLTLRGAACLAASDVVLYDGLSNVAMLSHAPNAQHICVGKHGQSRIWKQEEIIAEMLQHVSHGKTVARLKGGDPAVFARTAEEVDALKAAEIPFEIVPGITAALAAGSYAGIPVTHRKWASAVALVTGHEEPDKPESALDWDALAKFPGTLVIYMGVTTAETWTRALLDAGKPADTPAAILRRVSLPDQQSIHCRLDEVTDHLTPASKFRPPAIVILGAVTKLAETMSWFEHRPLFGTRILVTRPENQSEELAAGLRELGAEVTSQPAITISAPESWDEVDRCLNQITAGDTLVFASRNGVRFLAKRWTENGLDARHFAGVRIAAVGTRTAEALQEHGLRADIVPDDFTAEGLASTLSPDAQDRRFWLIRASRGRNVLAETLQNAGGNVDQIVTYRNEDTAVADPHIADQLQQGSFDWVTVTSSAIARSLHNLYGDALFQTKLASISPITTQTLSEIDSLNASPVAAEATTFTMAGLIEAILKHKQES
>NZ_CP036262.1|WP_145354568.1|6779015_6779294_-|30S-ribosomal-protein-S20
MPNSLSAKKRLRQNEKLRQANRAIRTGLRSQIRKVREAVAGGQLETADAEGRVASRKIDKACARGVLHKNTAARTKSRIQHLIKKAKAEAAA
>NZ_CP036262.1|WP_145354578.1|6793020_6794457_+|3-isopropylmalate-dehydratase-large-subunit
MSDSTAPAGSPQTMFEKIWNNHVVHSEPGKQAILYIDLHLVHEVTSPQAFEGLRINNRTVRRPERTIATPDHNVPTSDRSLPIADPIAKIQIETLRKNCSEFDVQLFDIDDVRQGIVHVIGPENGYTQPGMTIVCGDSHTATHGAFGSLAFGIGTSEVEHVLATQTLLQYKPKTFELRVDGELAPGVTAKDMILYLIGQIGTAGGTGYVLEFTGDCMTALSMEERMTVCNMSIEAGARAGMIAPDQTTFDYLKGRPQAPQGAAFDAAVAKWKQLPSDAGAQYDLSRTFQGSDIQPQVTWGTNPGQVRSVTDSTPNPSDFSDPTEQKTTANALEYMGLEAGTRLTDVSINRVFIGSCTNARIEDLRAAAAVAKGHHVSDSVNAMVVPGSGQVKRQAEKEGLDQIFKEAGFDWREAGCSMCLAMNPDKLEPGERCASTSNRNFEGRQGKGGRTHLVSPAMAAAAAVSGHFVDIRDWKYQS
>NZ_CP036262.1|WP_145354579.1|6794510_6795101_+|3-isopropylmalate-dehydratase-small-subunit
MQNFTIHTGVVATMDRANVDTDQIIPKQFLKRIERTGFGEFLFFDWRYEEDGKTPNPTFELNQVDVKGASVLVTRRNFGNGSSREHAVWALDDFGIRCVIAPSFADIFFNNCFKNGLLPITLSEADIDILFEKTKAQSPYQITVDLETQTITDNQGFERKFEVEPYRRHCLMNGLDDIALTLEHEAKITEFENANA
>NZ_CP036262.1|WP_145355904.1|6795939_6796500_-|hypothetical-protein
MIHTFDEAYQFVLKNKVCTVFGSRGSPHPSLWGSTDLSEEKPKAGGWSPKVKAVWDWKTRIPQTYPDEVFYGKIPGGDAVLMEMQYFRDVHYKEAYQPVGELNSLTQEVYDFIRLEASFTGPLRKRAIASLACTKSQFDTALKNLQVSLNIVRSNDPALKNDFWITMREMHLEIVQQHERDGLLPS
>NZ_CP036262.1|WP_145354580.1|6796897_6797737_+|hypothetical-protein
MPPETQPVSSPAKPRRNWIIIALLVLFISPIVLTVGVVCLLAFVAVLGGSAAIEQAKLQTEAKLQTEATVVSTQAFSDAPSPGDPLIAEVESPQESPIVESPFVEVDETPRTPEPTSLRFNDLTFSLRFVDKNDSTGTLNEYIPDGETLERWTQMIAVRDQPINVDPATVAQGAAEALQKINPQAPYKLWQSDDGLSHGIDFATWQGDIAEYNIFVYTRSADKKSIASYQYAERAYGDERQAFLDDLKNRRKDLIGEVTEFRFPVLTEQAPPYQLISQP
>NZ_CP036262.1|WP_145354581.1|6798205_6799909_+|solute:sodium-symporter-family-transporter
MLTIVSFVFFTALVGVLTWLITRHKETDSADGYFLAGRSLGAGVIAGSLLLTNLSTEQLVGLNGDAYTNGLSVMAWEVVAGVSLVLMAVFFLPRYLRRGITTIPEFLAGRYNDTTQLITNFIFILAYMMILLPIILYTGAMGLKEILAISDLTGIESETATLWLTVWTIGIIGSIYAIFGGLRSVAVSDTLNGFGLLVGGGLIAYFGLSAVGDGSALEGLSTLRETHPEKFNSLGSADSSVPWPTLFSGVLLLNLFYWTTNQQIIQRTFAASTLAEGQKGVLLAATFKILAPLILVLPGIIAFHLYGQGDSPIPQDQAYGTLVRNVLPTSLTGFFAAALVGAILSSFNSALNATATLFSLGFYRKLIRPTASDHETVRMGRIFGTIIALAAMTMAPMLAGQDSIFGYLQKMNGLYFIPIFAVVLVGMLSKKTPAIAANIALVVGVVVIFCGYFAPGFSSVVGQIHEFHFLGIVFVSLVAMMLGFAAIAPRPSHQHSSAGQGSAAKSDLAADQPYAPLQTGSEGLQTDDSSDDEFPPSPIDMTPWPLALPAGITLAIIVVGIYAWFAI
>NZ_CP036262.1|WP_145354582.1|6800344_6801385_+|AAA-domain-containing-protein
MSDAISSSGSKPDTEPTLSDNDVQAIDDLRVAHSKLKTELARVIVGQQAVIDQLVICLFARRHALLMGVPGLAKTLLVSKLAETLSLHFSRIQFTPDLMPMDITGTDILQDNAEGRREFHFVKGPVFANIVLADEINRAPPKTQAAMLEAMQEQRVTVVGKTYELPSPFMVLATQNPVEQEGTYPLPEAQLDRFMSLIELDYPNEAEEIQIAKSTTGGDLPELAHLLTGEKILEHQALVRRVPVPDHIYTYAARLVRKTRPQGESAPSWLPPLVSWGAGPRAVQNLILGAKSRAALLGSYMVRLEDVQEVAAAVLTHRIITTFAAQAEGIAAKDIVKRLIEESNES
>NZ_CP036262.1|WP_145354583.1|6801384_6802296_+|DUF58-domain-containing-protein
MFTGRQPREFLDTKILARLAGMPLFARRAMQGNVSGKHTSPHRGASVEFAEYRKYVPGDDLRRLDWRAYGRSDRFYIKEFEADTNLRCCVVLDTSGSMDFGTTGTTKIQYARQIAASLGYLAVQQGDAIGLHCFADGIVKNVPAKRNAAHLSLIFDTLEQAIPEGPTQLISVLHELAETIRQRALIVVISDFFVDPAELRGCFEHLRFRKHDLAAFQLLDPAELEFTFQRPTRFLDMEGGPAIFAEPNVIADRYQTALNEYLKQLQQIVLETGVDYHRTRIDEPFEQALMRFLVGRTRGRGVR
>NZ_CP036262.1|WP_145354584.1|6802292_6804317_+|hypothetical-protein
MSFLQPWMLLALPLVALPVIIHLINQRRFQTMPWAAMMFLLAANRMSRGYARLRQWLILLFRMLAIAGLLFVISRPLASGWLGATAGGGADATIVILDRSPSMQQIGTGSNSSKLDTARRQLSDALATLGTSRLVLIDSGDSSARELESIEAISDATDTGPAGNTADLAGMLKTAYDYVKANRVGRADVWIVSDLRESDWESGSGRWDALRDNFASLPQTTKFHLLAYSEPTAQNRSIRVTNVRRQQQGDTTNLLVSLSLSGDENNTAEGEFPLQFEIEGARSETTIALTGGSAEIKDHPIPIDSQLVRGWGRVSIPADTNPADNDAYFVFAEPAPRKTILVSDDPETSRPLLLAAQISPDPNVAATAETVNRDQLATIPWEEVALLVWQGDLPSAAEQKPIDAFVQAGGQVLFFPPKIIGSQQAYGLSWQPWISDDKGAEVSNWRGDEDLLANTISGASLPVGKLKIHKYAGLKGEYTPLASLDEQHPLLVRANRFTNDPAGNRDTTSLSGPPGIYFCTTTPNPGDSTLARDGVVLYVAIQRAILRGSEALGDTRSLDAGASEAVDWRAVSVNEDAISSQYGIQPGIYETSQKLLAINRSKAEDSATLVSDQKLESLFQGLDFSRVDDQAGSLRSLVNEIWRLFLIIMIVAMIVEAALCLPQKRTANEGAATP
>NZ_CP036262.1|WP_145354585.1|6804313_6806506_+|hypothetical-protein
MNRTQALTFEWSPWTLALSVVLIVAGAIFCWLAWRRSGYRRVIGWLELLRFCLIAAGVVLLNQPEWVQEYRPKEKPTVAVLYDASDSMTTMDAVRSTGGPAVTRHEQVAPLSEAETWSGLQDRFNVVIEPFASPESEDGSNLTAPLSGVIDQHPNLLGVVLASDGDWNLGSPPVEAAARLRGKGVPVFSVPVGRSSQLPDLELLSFDVPTFGIQGKAVRIPFTIESALPREYSTTVVLRSSEGDEISKDVLVAAMGRTNDSLIWQPPANGDFTLTLEVPPHSSETLTENNQRTAPIQIREERLRVLVIESVPRWEYRYLRNALSRDPGIEVSCLLFHPQLDKVGGGNADYISEFPAGLDQLSPYDVVFLGDVGIDDGQLTVEQCDQLKGLVEQQASGLVFIPGWQGRQSGLLETSLKELYPVVMDPLQPDGWGSRTASHFELTEIGQRSLLTKLADTREENAEIWESLPGFQWYAPVIKARPGSEVLAVHKDISNEYGRLPLLATRTYGTGKVLFMGTDGAWRWRKGVEDLYHYRFWGQVVRWMAYQRNMAKGETMRLYYSPEQPQVRQTVTLTANVMEENGEPLVSGNVSARIVGPSGRGQTVQFTSQGDQWGAFSGRFRSTESGEHSVTLSCQQTGATLETTVYVQGAALERIGKPARPEVLEEISRISRGQVIPIDKLESIRNALQTLPDPPPAIRRLQLWSHPLIAGTMVFLLGLFWIGRKAVGLI
>NZ_CP036262.1|WP_145354586.1|6806527_6809830_+|hypothetical-protein
MNKPSTRQHQKLVIPQSLENQLDQYRRQVWKIKTIEAIALALCGLLIGFLIVFALDRLFDTPAVIRLLVFAAAAIVCGVIPLFFHRWIWQHRRTEQLARLLSRRMPQLGDQLLGVIELTHNESEQHRSPALCEAAMQQVAEVSSKRDLRKATPPSRYRSWSGIAVLTGCGAAALMLLFPAATSNAWARFLAPWKQTERYTFTHLDEIPNQIIVAHGESFPLDVRLTESTEWHPDTAQVSIGSRPPIETSIEQEGYQFELPPLIEDAALALRVGDARREIAVVPKLRPELRELTAEVTLPEYLQRTKGIEKDLRSGMAAIVKGSQAVVRAKISRPLTAAHVNGEAVNVQSDQFVSTTVPVEQMADWKLDWQDEFGLAGREPFSLSIEAHEDEAPTVACENLQRTSVVLDSELLNFRIKANDDFGIRRVGIQWSSLNDQFVDEPIEGSRALAGGSPESESMDIQGTFSANSLGIPAQALHLRMWAEDYLPDRPPIYSAPYTVFVLTPDQHAIWMAEQLNKWHRQALEVRDRERQLFEANKELRSMTADELDRPEARRRLERQAQAERTNGRRLSKLTGAGEELVRQAARNPEIGVGHLDRWAEMLQVLQDISDNRMPNVADLLQEASEQSKLAKLGNTPPKPQGPQAGKVRATGSGGTPREEEPDPENKTPPAPTIADVESNQQPANEPAPSEEDAPPKKPSSPSLGLAKTTLIGPGGEPKEPPPPANDTVDKAVHEQENLLAEFEKISDELNQILGNLEGSTLVKRLKAAARKQYAIGGDLTEDIDSTFGRTKFGDKKVADEKTVQEKLAHLQTSEEESSQDVSRIMDDMHAYFERRRLTNFKTILEDMKKEDVVGGLRQLGSDLVSHQATSVAQCDYWSDTLDRWAEDLVDPASNGSCPGGKSPGSLPPSLVLEVLHVLEAEVKLREETRVAEQAREVTEEEQFQTEAKRLSRDQNGLSKRILKVVEAIEALPEGAARFAKDIKLLEGVIPVMNDATEILRSPDTGQQAIAAETEAIERLLESKRINPSGGGGGGGSTPGGGGGGTTTDTAIVLMGKGINKNEVREDRAISQSTGETGPALPAEFRAGLDRYFNELEQVQ

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4763889-4763912	0	1.0
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6647570-6647593	0	1.0
NZ_CP036262_20	20.1\|6240444\|44\|NZ_CP036262\|CRISPRCasFinder	6240444-6240487	44	NZ_CP036262.1	6240531-6240574	0	1.0
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	2601743-2601769	1	0.963
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6116579-6116605	1	0.963
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6116884-6116910	1	0.963
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4763810-4763833	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4763968-4763991	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6773062-6773085	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	2845064-2845087	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	3003203-3003226	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4437210-4437233	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4437405-4437428	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4437502-4437525	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4577353-4577376	1	0.958
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6240675-6240698	1	0.958
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	2601577-2601603	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	2601660-2601686	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	2623476-2623502	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6116681-6116707	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6116783-6116809	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	1921445-1921471	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	1927738-1927764	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	1928040-1928066	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	2289748-2289774	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	3661923-3661949	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6773027-6773053	2	0.926
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP036262.1	6773097-6773123	2	0.926
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4465048-4465071	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6773027-6773050	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6966577-6966600	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6966678-6966701	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	6966879-6966902	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP036262.1	4437308-4437331	2	0.917
NZ_CP036262_20	20.1\|6240444\|44\|NZ_CP036262\|CRISPRCasFinder	6240444-6240487	44	NZ_CP036262.1	4724885-4724928	2	0.955
NZ_CP036262_20	20.1\|6240444\|44\|NZ_CP036262\|CRISPRCasFinder	6240444-6240487	44	NZ_CP036262.1	5399770-5399813	2	0.955
NZ_CP036262_20	20.1\|6240444\|44\|NZ_CP036262\|CRISPRCasFinder	6240444-6240487	44	NZ_CP036262.1	1891447-1891490	2	0.955
NZ_CP036262_20	20.1\|6240444\|44\|NZ_CP036262\|CRISPRCasFinder	6240444-6240487	44	NZ_CP036262.1	3247995-3248038	2	0.955

1. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4763889-4763912, mismatch: 0, identity: 1.0

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgcgccgttc	Protospacer
************************

2. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6647570-6647593, mismatch: 0, identity: 1.0

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgcgccgttc	Protospacer
************************

3. spacer 20.1|6240444|44|NZ_CP036262|CRISPRCasFinder matches to position: 6240531-6240574, mismatch: 0, identity: 1.0

tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	CRISPR spacer
tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	Protospacer
********************************************

4. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 2601743-2601769, mismatch: 1, identity: 0.963

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggctcgcgccgttc	Protospacer
*** ***********************

5. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6116579-6116605, mismatch: 1, identity: 0.963

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggctcgcgccgttc	Protospacer
*** ***********************

6. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6116884-6116910, mismatch: 1, identity: 0.963

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggctcgcgccgttc	Protospacer
*** ***********************

7. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4763810-4763833, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggcttgcgccgttc	Protospacer
**************.*********

8. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4763968-4763991, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggcttgcgccgttc	Protospacer
**************.*********

9. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6773062-6773085, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
cagcccggacggctcgcgccgttc	Protospacer
*** ********************

10. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 2845064-2845087, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggctcgcgccgttc	Protospacer
** *********************

11. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 3003203-3003226, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggcttgcgccgttc	Protospacer
**************.*********

12. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4437210-4437233, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggctcgcgccgttc	Protospacer
** *********************

13. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4437405-4437428, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggctcgcgccgttc	Protospacer
** *********************

14. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4437502-4437525, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggctcgcgccgttc	Protospacer
** *********************

15. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4577353-4577376, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggctcgcgccgttc	Protospacer
** *********************

16. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6240675-6240698, mismatch: 1, identity: 0.958

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggcttgcgccgttc	Protospacer
**************.*********

17. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 2601577-2601603, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

18. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 2601660-2601686, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

19. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 2623476-2623502, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaattggccggacggctcgcgccgttc	Protospacer
***. **********************

20. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6116681-6116707, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

21. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6116783-6116809, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

22. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 1921445-1921471, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaagggccggacggctcgcgccgttc	Protospacer
*** .**********************

23. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 1927738-1927764, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

24. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 1928040-1928066, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

25. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 2289748-2289774, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaaaaggccggacggcttgcgccgttc	Protospacer
*** *************.*********

26. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 3661923-3661949, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aatcgggccggacggctcgcgccgttc	Protospacer
** *.**********************

27. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6773027-6773053, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aaacagcccggacggctcgcggcgttc	Protospacer
****** ************** *****

28. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to position: 6773097-6773123, mismatch: 2, identity: 0.926

aaacaggccggacggctcgcgccgttc	CRISPR spacer
aatcgggccggacggctcgcgccgttc	Protospacer
** *.**********************

29. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4465048-4465071, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggagggctcgcgcccttc	Protospacer
********* ********** ***

30. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6773027-6773050, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
cagcccggacggctcgcggcgttc	Protospacer
*** ************** *****

31. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6966577-6966600, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggcttgcgccgttc	Protospacer
** ***********.*********

32. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6966678-6966701, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggcttgcgccgttc	Protospacer
** ***********.*********

33. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 6966879-6966902, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggacggcttgcgccgttc	Protospacer
** ***********.*********

34. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to position: 4437308-4437331, mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
catgccggaccgctcgcgccgttc	Protospacer
** ******* *************

35. spacer 20.1|6240444|44|NZ_CP036262|CRISPRCasFinder matches to position: 4724885-4724928, mismatch: 2, identity: 0.955

tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	CRISPR spacer
tcttagcggaacggcgcgagccgtccggcaaccgcatcgaaaac	Protospacer
***************************** ******* ******

36. spacer 20.1|6240444|44|NZ_CP036262|CRISPRCasFinder matches to position: 5399770-5399813, mismatch: 2, identity: 0.955

tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	CRISPR spacer
tcttagcggaacggcgcgagccgtccggcaatcgcatagaaaac	Protospacer
***************************** *.************

37. spacer 20.1|6240444|44|NZ_CP036262|CRISPRCasFinder matches to position: 1891447-1891490, mismatch: 2, identity: 0.955

tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	CRISPR spacer
tcttagcggaacggcgcgagccgtccggcaatcgcatagaaaac	Protospacer
***************************** *.************

38. spacer 20.1|6240444|44|NZ_CP036262|CRISPRCasFinder matches to position: 3247995-3248038, mismatch: 2, identity: 0.955

tcttagcggaacggcgcgagccgtccggccaccgcatagaaaac	CRISPR spacer
tcttagcggaacggcgcgagacgtccggcaaccgcatagaaaac	Protospacer
******************** ******** **************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1585463-1585486	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1375810-1375833	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	986534-986557	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	751428-751451	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1582022-1582045	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	1114530-1114553	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	44104-44127	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	924982-925005	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	1114497-1114520	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	1113320-1113343	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	1113333-1113356	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	1113333-1113356	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	909775-909798	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	1113322-1113345	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1029953-1029976	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	1113322-1113345	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1042062-1042085	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	1114496-1114519	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	1113333-1113356	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	908330-908353	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	1113344-1113367	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	1113322-1113345	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	908330-908353	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1062047-1062070	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	1083947-1083970	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1685321-1685344	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	988334-988357	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1126475-1126498	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1149159-1149182	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1324635-1324658	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1460482-1460505	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1045458-1045481	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1134227-1134250	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	849081-849104	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1067710-1067733	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	985720-985743	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	985709-985732	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1064412-1064435	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	1040412-1040435	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1134216-1134239	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1127592-1127615	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1155215-1155238	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	1149169-1149192	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1039892-1039915	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1127592-1127615	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1155215-1155238	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1127592-1127615	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1039915-1039938	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1127596-1127619	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1155215-1155238	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1155215-1155238	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1155215-1155238	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1039915-1039938	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1057018-1057041	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1037689-1037712	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1085639-1085662	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1131795-1131818	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1039915-1039938	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1127591-1127614	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1039915-1039938	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1039915-1039938	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1155216-1155239	2	0.917
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP013419	Burkholderia sp. MSMB0266 plasmid pMSMB0266, complete sequence	197680-197703	3	0.875
NZ_CP036262_2	2.1\|152851\|25\|NZ_CP036262\|CRISPRCasFinder	152851-152875	25	NC_011892	Methylobacterium nodulans ORS 2060 plasmid pMNOD01, complete sequence	80658-80682	4	0.84
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1062044-1062070	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	1083944-1083970	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1685318-1685344	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	988331-988357	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1126472-1126498	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1149156-1149182	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1324632-1324658	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1460479-1460505	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1045455-1045481	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1134224-1134250	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	849078-849104	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1067707-1067733	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	985717-985743	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	985706-985732	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1064409-1064435	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	1040409-1040435	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1134213-1134239	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1127589-1127615	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1155212-1155238	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	1149166-1149192	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1039889-1039915	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1127589-1127615	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1155212-1155238	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1127589-1127615	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1039912-1039938	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1127593-1127619	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1155212-1155238	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1155212-1155238	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1155212-1155238	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1039912-1039938	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1057015-1057041	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1037686-1037712	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1085636-1085662	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1131792-1131818	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1039912-1039938	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1127588-1127614	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1039912-1039938	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1039912-1039938	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1155213-1155239	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1585463-1585489	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1375810-1375836	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	986534-986560	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	751428-751454	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1582022-1582048	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	1114530-1114556	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	44104-44130	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	924982-925008	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	1114497-1114523	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	1113320-1113346	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	1113333-1113359	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	1113333-1113359	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	909775-909801	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	1113322-1113348	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1029953-1029979	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	1113322-1113348	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1042062-1042088	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	1114496-1114522	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	1113333-1113359	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	908330-908356	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	1113344-1113370	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	1113322-1113348	5	0.815
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	908330-908356	5	0.815
NZ_CP036262_6	6.2\|1030319\|24\|NZ_CP036262\|PILER-CR	1030319-1030342	24	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	79357-79380	5	0.792
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_AP014579	Burkholderia sp. RPE67 plasmid p1, complete sequence	436300-436326	6	0.778
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP013419	Burkholderia sp. MSMB0266 plasmid pMSMB0266, complete sequence	197680-197706	6	0.778
NZ_CP036262_15	15.4\|5147706\|30\|NZ_CP036262\|CRT	5147706-5147735	30	NZ_LR134459	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 17, complete sequence	90824-90853	6	0.8
NZ_CP036262_16	16.6\|5465685\|30\|NZ_CP036262\|CRT	5465685-5465714	30	NZ_CP022581	Gordonia rubripertincta strain CWB2 plasmid pGCWB2, complete sequence	58981-59010	6	0.8
NZ_CP036262_16	16.2\|5465445\|30\|NZ_CP036262\|CRT	5465445-5465474	30	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	1308112-1308141	7	0.767
NZ_CP036262_16	16.6\|5465685\|30\|NZ_CP036262\|CRT	5465685-5465714	30	MT889364	Arthrobacter phage Yavru, complete genome	6953-6982	7	0.767
NZ_CP036262_6	6.1\|1030241\|27\|NZ_CP036262\|PILER-CR	1030241-1030267	27	NZ_CP020040	Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence	79357-79383	8	0.704
NZ_CP036262_10	10.1\|2304076\|30\|NZ_CP036262\|CRISPRCasFinder	2304076-2304105	30	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1854901-1854930	8	0.733
NZ_CP036262_15	15.2\|5147598\|30\|NZ_CP036262\|CRT	5147598-5147627	30	NC_048758	Serratia phage Parlo, complete genome	10193-10222	8	0.733
NZ_CP036262_16	16.2\|5465445\|30\|NZ_CP036262\|CRT	5465445-5465474	30	NC_015952	Streptomyces violaceusniger Tu 4113 plasmid pSTRVI02, complete sequence	190809-190838	8	0.733
NZ_CP036262_16	16.2\|5465445\|30\|NZ_CP036262\|CRT	5465445-5465474	30	NZ_CP009439	Streptomyces glaucescens strain GLA.O plasmid pSglau1, complete sequence	152852-152881	8	0.733
NZ_CP036262_16	16.2\|5465445\|30\|NZ_CP036262\|CRT	5465445-5465474	30	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	114583-114612	8	0.733
NZ_CP036262_16	16.6\|5465685\|30\|NZ_CP036262\|CRT	5465685-5465714	30	MH651182	Gordonia phage Neville, complete genome	19661-19690	8	0.733
NZ_CP036262_16	16.6\|5465685\|30\|NZ_CP036262\|CRT	5465685-5465714	30	MK967378	Gordonia phage Trax, complete genome	19970-19999	8	0.733
NZ_CP036262_16	16.6\|5465685\|30\|NZ_CP036262\|CRT	5465685-5465714	30	NC_010627	Paraburkholderia phymatum STM815 plasmid pBPHY02, complete sequence	338330-338359	8	0.733

1. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

2. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

3. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

4. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

5. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

6. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

7. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

8. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

9. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

10. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

11. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

12. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

13. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

14. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

15. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

16. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

17. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

18. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

19. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

20. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

21. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

22. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

23. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

24. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

25. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

26. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

27. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

28. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

29. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

30. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

31. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

32. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

33. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

34. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

35. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

36. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

37. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

38. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

39. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

40. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

41. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

42. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

43. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

44. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

45. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

46. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

47. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

48. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

49. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

50. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

51. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

52. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

53. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

54. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

55. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

56. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

57. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

58. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

59. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

60. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

61. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

62. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 2, identity: 0.917

caggccggacggctcgcgccgttc	CRISPR spacer
caggccggacggctcgatccgttc	Protospacer
****************  ******

63. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP013419 (Burkholderia sp. MSMB0266 plasmid pMSMB0266, complete sequence) position: , mismatch: 3, identity: 0.875

caggccggacggctcgcgccgttc	CRISPR spacer
caggcgggccggctcgcgccgttt	Protospacer
***** ** **************.

64. spacer 2.1|152851|25|NZ_CP036262|CRISPRCasFinder matches to NC_011892 (Methylobacterium nodulans ORS 2060 plasmid pMNOD01, complete sequence) position: , mismatch: 4, identity: 0.84

ggtcaccgaaacgcagtaccgcgat	CRISPR spacer
cgtcaccgacacgcagtaccgcggc	Protospacer
 ******** *************..

65. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

66. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cttcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

67. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

68. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

69. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

70. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

71. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

72. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

73. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

74. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

75. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

76. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

77. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cttcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

78. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cttcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

79. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

80. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

81. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

82. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

83. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

84. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

85. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

86. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

87. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

88. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

89. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

90. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

91. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

92. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

93. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

94. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

95. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

96. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

97. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

98. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

99. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

100. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

101. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

102. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

103. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

104. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

105. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

106. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

107. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

108. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

109. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

110. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

111. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

112. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

113. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

114. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

115. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

116. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

117. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

118. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

119. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

120. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

121. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

122. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

123. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

124. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

125. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

126. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.815

aaacaggccggacggctcgcgccgttc	CRISPR spacer
cctcaggccggacggctcgatccgttc	Protospacer
   ****************  ******

127. spacer 6.2|1030319|24|NZ_CP036262|PILER-CR matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 5, identity: 0.792

caggccggacggctcgcgccgttc	CRISPR spacer
gaggccggacggctcgcgcccccg	Protospacer
 ******************* ..

128. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_AP014579 (Burkholderia sp. RPE67 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.778

aaacaggccggacggctcgcgccgttc	CRISPR spacer
gaagaggccggaccgctcgcgccggaa	Protospacer
.** ********* **********

129. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP013419 (Burkholderia sp. MSMB0266 plasmid pMSMB0266, complete sequence) position: , mismatch: 6, identity: 0.778

aaacaggccggacggctcgcgccgttc	CRISPR spacer
ttgcaggcgggccggctcgcgccgttt	Protospacer
  .***** ** **************.

130. spacer 15.4|5147706|30|NZ_CP036262|CRT matches to NZ_LR134459 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 17, complete sequence) position: , mismatch: 6, identity: 0.8

acagggtggagaacagggtggtgagcaggg	CRISPR spacer
cccggcaggagaacagcgtggtgagcagcg	Protospacer
 * **  ********* *********** *

131. spacer 16.6|5465685|30|NZ_CP036262|CRT matches to NZ_CP022581 (Gordonia rubripertincta strain CWB2 plasmid pGCWB2, complete sequence) position: , mismatch: 6, identity: 0.8

gcctgactcgccgcctgactcgccacctga	CRISPR spacer
gccaccgtcgccgcccgagtcgccacctga	Protospacer
***    ********.** ***********

132. spacer 16.2|5465445|30|NZ_CP036262|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 7, identity: 0.767

gcctgactcgccgcctgactcgccgcctga	CRISPR spacer
cgcggcgccgccgcctgacgcgccgcctga	Protospacer
  * *  .*********** **********

133. spacer 16.6|5465685|30|NZ_CP036262|CRT matches to MT889364 (Arthrobacter phage Yavru, complete genome) position: , mismatch: 7, identity: 0.767

gcctgactcgccgcctgactcgccacctga	CRISPR spacer
gccggactcgccgccggactcgcggccgcg	Protospacer
*** *********** ******* .**  .

134. spacer 6.1|1030241|27|NZ_CP036262|PILER-CR matches to NZ_CP020040 (Streptomyces sp. 3211 isolate 3 plasmid p3211-1, complete sequence) position: , mismatch: 8, identity: 0.704

aaacaggccggacggctcgcgccgttc	CRISPR spacer
gccgaggccggacggctcgcgcccccg	Protospacer
.   ******************* ..

135. spacer 10.1|2304076|30|NZ_CP036262|CRISPRCasFinder matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 8, identity: 0.733

gcgtaccgccaatatcgtttccagggcggt	CRISPR spacer
tgtcattgccaatatcgtttccggcgcggt	Protospacer
   .*..***************.* *****

136. spacer 15.2|5147598|30|NZ_CP036262|CRT matches to NC_048758 (Serratia phage Parlo, complete genome) position: , mismatch: 8, identity: 0.733

gcaaggtggagagcaaggtggagagcaggg	CRISPR spacer
attacctggagagcaaggtggggatcagga	Protospacer
.. *  ***************.** ****.

137. spacer 16.2|5465445|30|NZ_CP036262|CRT matches to NC_015952 (Streptomyces violaceusniger Tu 4113 plasmid pSTRVI02, complete sequence) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccgcctga	CRISPR spacer
ctcgtgttcgccgccggactcgccgcctgg	Protospacer
 .*  ..******** *************.

138. spacer 16.2|5465445|30|NZ_CP036262|CRT matches to NZ_CP009439 (Streptomyces glaucescens strain GLA.O plasmid pSglau1, complete sequence) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccgcctga	CRISPR spacer
ctcgccctcgccgccggactcgacgcctgg	Protospacer
 .*   ********* ****** ******.

139. spacer 16.2|5465445|30|NZ_CP036262|CRT matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccgcctga	CRISPR spacer
atcggcctcgccgcctggctcgccgccgcg	Protospacer
..* * ***********.*********  .

140. spacer 16.6|5465685|30|NZ_CP036262|CRT matches to MH651182 (Gordonia phage Neville, complete genome) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccacctga	CRISPR spacer
ctggaactcgccgcccgactcgccaccagg	Protospacer
 .  .**********.*********** *.

141. spacer 16.6|5465685|30|NZ_CP036262|CRT matches to MK967378 (Gordonia phage Trax, complete genome) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccacctga	CRISPR spacer
ctggaactcgccgcccgactcgccaccagg	Protospacer
 .  .**********.*********** *.

142. spacer 16.6|5465685|30|NZ_CP036262|CRT matches to NC_010627 (Paraburkholderia phymatum STM815 plasmid pBPHY02, complete sequence) position: , mismatch: 8, identity: 0.733

gcctgactcgccgcctgactcgccacctga	CRISPR spacer
ttctcactcgccgcctgacttgccaaccct	Protospacer
 .** ***************.**** *.

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

6252648 : 6326028

Tetraselmis_virus(25.0%)

transposase,protease

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145354245.1\|6252648_6254388_+\|protease	matrixin family metalloprotease	W8QE20	Anopheles_minimus_irodovirus	1.8e-07	34.8
WP_145354246.1\|6254651_6255305_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_145354247.1\|6255304_6257911_+	protein kinase	A0A146JFA3	Tokyovirus	2.1e-15	23.6
WP_145354248.1\|6257907_6259140_+	hypothetical protein	NA	NA	NA	NA
WP_145354249.1\|6259134_6260523_-	sulfatase-like hydrolase/transferase	A0A2P0VMN7	Tetraselmis_virus	6.8e-21	28.5
WP_145354250.1\|6260602_6262075_-	sulfatase-like hydrolase/transferase	NA	NA	NA	NA
WP_145354251.1\|6262739_6263330_+	histidine phosphatase family protein	NA	NA	NA	NA
WP_145354252.1\|6263675_6264539_+	hypothetical protein	NA	NA	NA	NA
WP_145354253.1\|6264641_6265763_-	ABC transporter permease subunit	NA	NA	NA	NA
WP_145354254.1\|6265763_6268541_-	ribosome-associated ATPase/putative transporter RbbA	A0A2H4PQG7	Staphylococcus_phage	2.3e-20	29.0
WP_145354255.1\|6268614_6269625_-	HlyD family efflux transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_145354256.1\|6270026_6271073_+	dihydroorotate dehydrogenase-like protein	NA	NA	NA	NA
WP_145354257.1\|6271169_6271760_+	hypothetical protein	NA	NA	NA	NA
WP_145354258.1\|6272348_6273518_+	polyphosphate kinase 2	NA	NA	NA	NA
WP_145355818.1\|6274175_6275690_-	DUF1254 domain-containing protein	NA	NA	NA	NA
WP_145354259.1\|6275807_6276851_-	DUF1214 domain-containing protein	A0A2P0VP21	Tetraselmis_virus	8.9e-42	36.1
WP_145354260.1\|6276948_6278391_-	DUF1254 domain-containing protein	M1I2Z8	Paramecium_bursaria_Chlorella_virus	7.5e-124	49.7
WP_145355821.1\|6278491_6280012_-	DUF1214 domain-containing protein	NA	NA	NA	NA
WP_145354261.1\|6280877_6281354_+	NYN domain-containing protein	NA	NA	NA	NA
WP_145354262.1\|6281636_6282989_+	amidohydrolase family protein	NA	NA	NA	NA
WP_145354263.1\|6283026_6283254_-	hypothetical protein	NA	NA	NA	NA
WP_145354264.1\|6287712_6288126_-	hypothetical protein	NA	NA	NA	NA
WP_145354265.1\|6288846_6289893_+	hypothetical protein	NA	NA	NA	NA
WP_145354266.1\|6289965_6290430_+	hypothetical protein	NA	NA	NA	NA
WP_145354267.1\|6291158_6291818_+	hypothetical protein	NA	NA	NA	NA
WP_145355824.1\|6292075_6292792_+	WecB/TagA/CpsF family glycosyltransferase	NA	NA	NA	NA
WP_145354268.1\|6293343_6294276_+	2OG-Fe(II) oxygenase	NA	NA	NA	NA
WP_145354269.1\|6294325_6295786_+	oligosaccharide flippase family protein	NA	NA	NA	NA
WP_145354270.1\|6295858_6296767_+	sulfotransferase domain-containing protein	NA	NA	NA	NA
WP_145354271.1\|6296759_6297521_+	sulfotransferase	NA	NA	NA	NA
WP_145354272.1\|6297602_6298937_+	hypothetical protein	NA	NA	NA	NA
WP_145354273.1\|6299053_6300388_+	polysaccharide pyruvyl transferase family protein	NA	NA	NA	NA
WP_145354274.1\|6300447_6301497_+	glycosyltransferase	NA	NA	NA	NA
WP_145354275.1\|6301525_6302425_+	sulfotransferase domain-containing protein	NA	NA	NA	NA
WP_145354276.1\|6302446_6303424_+	sulfotransferase	NA	NA	NA	NA
WP_145354277.1\|6303460_6304060_+	transferase	NA	NA	NA	NA
WP_145354278.1\|6304094_6305153_+	glycosyltransferase	NA	NA	NA	NA
WP_145354279.1\|6305142_6306231_+	Gfo/Idh/MocA family oxidoreductase	NA	NA	NA	NA
WP_145354280.1\|6306227_6307235_+	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_145354281.1\|6307221_6308469_+	glycosyltransferase	NA	NA	NA	NA
WP_145354282.1\|6308835_6309165_-\|transposase	transposase	NA	NA	NA	NA
WP_145354283.1\|6312867_6313116_+	glycosyltransferase	NA	NA	NA	NA
WP_145354284.1\|6313261_6314428_+	glycosyltransferase	NA	NA	NA	NA
WP_145354285.1\|6314512_6315400_+	sugar nucleotide-binding protein	A0A1V0SL94	Klosneuvirus	2.4e-19	24.1
WP_145354286.1\|6315797_6316121_-\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_145354287.1\|6316151_6317132_-\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_145354288.1\|6319017_6319890_+	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	1.3e-94	61.3
WP_145354289.1\|6322236_6322536_+	hypothetical protein	NA	NA	NA	NA
WP_145354290.1\|6322622_6323738_+\|transposase	IS1380 family transposase	NA	NA	NA	NA
WP_145354291.1\|6324191_6325286_+	acyltransferase family protein	NA	NA	NA	NA
WP_145354292.1\|6325341_6326028_-\|transposase	transposase	NA	NA	NA	NA

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP036262

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection