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_CP026729	Bifidobacterium catenulatum subsp. kashiwanohense strain APCKJ1 chromosome, complete genome	8 crisprs	cas3,RT,csa3,DEDDh,WYL,c2c9_V-U4	0	0	3	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP026729_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_1

37550-37624

Orphan

Consensus_repeat	Method
TGTCCGATTCTGCAGAATCGGACA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP026729_1

>merge|NZ_CP026729|1|37550-37624|CRISPRCasFinder
TGTCCGATTCTGCAGAATCGGACAACCAAACCACGAAAAGTGAGCCACAGTTGTCCGATTCTGCAGAATCGGACA

>NZ_CP026729|1|1|37550-37624|CRISPRCasFinder
TGTCCGATTCTGCAGAATCGGACA	ACCAAACCACGAAAAGTGAGCCACAGT
TGTCCGATTCTGCAGAATCGGACA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154303336.1\|31715_32096_+\|DUF3073-family-protein	unknown	unknown	gnl\|CDD\|378620
NZ_CP026729.1\|WP_154303342.1\|42543_44640_-\|Stk1-family-PASTA-domain-containing-Ser/Thr-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP026729.1\|WP_154303335.1\|30487_31588_-\|tryptophan--tRNA-ligase	unknown	unknown	gnl\|CDD\|234866
NZ_CP026729.1\|WP_154303334.1\|27195_28824_+\|sodium/solute-symporter	unknown	unknown	gnl\|CDD\|271369
NZ_CP026729.1\|WP_033501551.1\|44636_45581_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP026729.1\|WP_154303338.1\|33000_35448_+\|glycogen/starch/alpha-glucan-family-phosphorylase	unknown	unknown	gnl\|CDD\|273967
NZ_CP026729.1\|WP_033501566.1\|25045_26887_+\|threonine/serine-exporter-family-protein	unknown	unknown	gnl\|CDD\|377697
NZ_CP026729.1\|WP_070097852.1\|38979_39465_-\|cell-division-protein-CrgA	unknown	unknown	gnl\|CDD\|179394
NZ_CP026729.1\|WP_154303341.1\|40407_41499_+\|class-E-sortase	unknown	unknown	gnl\|CDD\|320679
NZ_CP026729.1\|WP_154303337.1\|32207_32645_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380033
NZ_CP026729.1\|WP_154303343.1\|45577_47044_-\|penicillin-binding-protein-2	unknown	unknown	gnl\|CDD\|274573
NZ_CP026729.1\|WP_033501548.1\|50284_50800_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238017
NZ_CP026729.1\|WP_154304349.1\|41687_42332_+\|C26-family-cysteine-hydrolase-domain-containing-family	unknown	unknown	gnl\|CDD\|181107
NZ_CP026729.1\|WP_033501558.1\|35668_35896_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_033501555.1\|39582_40350_+\|DUF881-domain-containing-protein	unknown	unknown	gnl\|CDD\|377575
NZ_CP026729.1\|WP_033501564.1\|28982_29528_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_033501603.1\|48662_50279_-\|serine/threonine-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP026729.1\|WP_154303344.1\|47040_48666_-\|FtsW/RodA/SpoVE-family-cell-cycle-protein	unknown	unknown	gnl\|CDD\|223843
NZ_CP026729.1\|WP_033501563.1\|29520_30393_+\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	unknown	unknown	gnl\|CDD\|378065
NZ_CP026729.1\|WP_154303339.1\|36082_36877_+\|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl\|CDD\|223777

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154303336.1\|31715_32096_+\|DUF3073-family-protein	gnl\|CDD\|378620	pfam11273, DUF3073, Protein of unknown function (DUF3073). This family of proteins with unknown function appears to be restricted to Actinobacteria.	2.09016e-19
NZ_CP026729.1\|WP_154303342.1\|42543_44640_-\|Stk1-family-PASTA-domain-containing-Ser/Thr-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.	4.41824e-128
NZ_CP026729.1\|WP_154303335.1\|30487_31588_-\|tryptophan--tRNA-ligase	gnl\|CDD\|234866	PRK00927, PRK00927, tryptophanyl-tRNA synthetase; Reviewed.	2.98248e-113
NZ_CP026729.1\|WP_154303334.1\|27195_28824_+\|sodium/solute-symporter	gnl\|CDD\|271369	cd11475, SLC5sbd_PutP, Na(+)/proline cotransporter PutP and related proteins; solute binding domain. Escherichia coli PutP catalyzes the Na+-coupled uptake of proline with a stoichiometry of 1:1. The putP gene is part of the put operon; this operon in addition encodes a proline dehydrogenase, allowing the use of proline as a source of nitrogen and/or carbon. This subfamily also includes the Bacillus subtilis Na+/proline cotransporter (OpuE) which has an osmoprotective instead of catabolic role. Expression of the opuE gene is under osmotic control and different sigma factors contribute to its regulation; it is also a putative CcpA-activated gene. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	2.14304e-178
NZ_CP026729.1\|WP_033501551.1\|44636_45581_-\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	1.18558e-109
NZ_CP026729.1\|WP_154303338.1\|33000_35448_+\|glycogen/starch/alpha-glucan-family-phosphorylase	gnl\|CDD\|273967	TIGR02093, Glycogen_phosphorylase, glycogen/starch/alpha-glucan phosphorylases. This family consists of phosphorylases. Members use phosphate to break alpha 1,4 linkages between pairs of glucose residues at the end of long glucose polymers, releasing alpha-D-glucose 1-phosphate. The nomenclature convention is to preface the name according to the natural substrate, as in glycogen phosphorylase, starch phosphorylase, maltodextrin phosphorylase, etc. Name differences among these substrates reflect differences in patterns of branching with alpha 1,6 linkages. Members include allosterically regulated and unregulated forms. A related family, TIGR02094, contains examples known to act well on particularly small alpha 1,4 glucans, as may be found after import from exogenous sources. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP026729.1\|WP_033501566.1\|25045_26887_+\|threonine/serine-exporter-family-protein	gnl\|CDD\|377697	pfam06738, ThrE, Putative threonine/serine exporter. ThrE is a family of bacterial and Archaeal proteins that catalyze the export of L-threonine from the cell. UniProtKB:Q79VD1 has been characterized as being necessary for this export. The domain exhibits 10 putative TMs and catalyzes the proton-motive-force-dependent efflux of threonine and serine.	2.52089e-37
NZ_CP026729.1\|WP_070097852.1\|38979_39465_-\|cell-division-protein-CrgA	gnl\|CDD\|179394	PRK02251, PRK02251, cell division protein CrgA.	2.6445e-49
NZ_CP026729.1\|WP_154303341.1\|40407_41499_+\|class-E-sortase	gnl\|CDD\|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	4.86596e-64
NZ_CP026729.1\|WP_154303337.1\|32207_32645_-\|hypothetical-protein	gnl\|CDD\|380033	pfam17844, SCP_3, Bacterial SCP ortholog. This domain is found in MSMEG_5817 gene product from M. smegmatis. It has been shown to be vital for mycobacterial survival within host macrophages. Crystal structure revealed a Rossmann-like fold alpha/beta two-layer sandwich forming a highly hydrophobic interface cavity and with high structural homology to the SCP family. Hence, it has been suggested that this domain may be involved in the interaction of apolar ligands through its hydrophobic cavity. Alanine-scanning mutagenesis of the hydrophobic cavity of MSMEG_5817 protein demonstrated that the conserved Val82 residue plays an important role in ligand binding.	2.7953e-43
NZ_CP026729.1\|WP_154303343.1\|45577_47044_-\|penicillin-binding-protein-2	gnl\|CDD\|274573	TIGR03423, pbp2_mrdA, penicillin-binding protein 2. Members of this protein family are penicillin-binding protein 2 (PBP-2), a protein whose gene (designated pbpA or mrdA) generally is found next to the gene for RodA, a protein required for rod (bacillus) shape in many bacteria. PBP-2 acts as a transpeptidase for cell elongation (hence, rod-shape). [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	7.36626e-93
NZ_CP026729.1\|WP_154304349.1\|41687_42332_+\|C26-family-cysteine-hydrolase-domain-containing-family	gnl\|CDD\|181107	PRK07765, PRK07765, aminodeoxychorismate/anthranilate synthase component II.	1.82234e-99
NZ_CP026729.1\|WP_033501548.1\|50284_50800_-\|FHA-domain-containing-protein	gnl\|CDD\|238017	cd00060, FHA, Forkhead associated domain (FHA); found in eukaryotic and prokaryotic proteins. Putative nuclear signalling domain. FHA domains may bind phosphothreonine, phosphoserine and sometimes phosphotyrosine. In eukaryotes, many FHA domain-containing proteins localize to the nucleus, where they participate in establishing or maintaining cell cycle checkpoints, DNA repair, or transcriptional regulation. Members of the FHA family include: Dun1, Rad53, Cds1, Mek1, KAPP(kinase-associated protein phosphatase),and Ki-67 (a human nuclear protein related to cell proliferation).	2.00253e-17
NZ_CP026729.1\|WP_033501555.1\|39582_40350_+\|DUF881-domain-containing-protein	gnl\|CDD\|377575	pfam05949, DUF881, Bacterial protein of unknown function (DUF881). This family consists of a series of hypothetical bacterial proteins. One of the family members YlxW from Bacillus subtilis is thought to be involved in cell division and sporulation.	2.21724e-47
NZ_CP026729.1\|WP_033501603.1\|48662_50279_-\|serine/threonine-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	2.73695e-68
NZ_CP026729.1\|WP_154303344.1\|47040_48666_-\|FtsW/RodA/SpoVE-family-cell-cycle-protein	gnl\|CDD\|223843	COG0772, FtsW, Bacterial cell division membrane protein [Cell division and chromosome partitioning].	3.4543e-76
NZ_CP026729.1\|WP_033501563.1\|29520_30393_+\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	gnl\|CDD\|378065	pfam08843, AbiEii, Nucleotidyl transferase AbiEii toxin, Type IV TA system. This family was recently identified as belonging to the nucleotidyltransferase superfamily. AbiEii is the cognate toxin of the type IV toxin-antitoxin 'innate immunity' bacterial abortive infection (Abi) system that protects bacteria from the spread of a phage infection. The Abi system is activated upon infection with phage to abort the cell thus preventing the spread of phage through viral replication. There are some 20 or more Abis, and they are predominantly plasmid-encoded lactococcal systems. TA, toxin-antitoxin, systems on plasmids function by killing cells that lose the plasmid upon division. AbiE phage resistance systems function as novel Type IV TAs and are widespread in bacteria and archaea. The cognate antitoxin is pfam13338.	5.70707e-28
NZ_CP026729.1\|WP_154303339.1\|36082_36877_+\|rhomboid-family-intramembrane-serine-protease	gnl\|CDD\|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	4.0477e-25

>NZ_CP026729.1|WP_154303339.1|36082_36877_+|rhomboid-family-intramembrane-serine-protease
MAYQRFSLFPDSPSFKDLCSARSMRYRWRNGDPVITVAIMVICVAVWIVETLLKIAWPAGYNSFVGTGVFMPALATHRPWTFITSMFLHQPASLWHILFNMLTLWCVGPVLERMMGHLPYLALYVLSGLGGSAGMMVWALFSQDGWLTSAYGASGALFGLFAAILVVYQRIGIDIRSMLIWMLINFLMPIITPNIAWQAHIGGFIIGGVFAWLLVSGLHALRGKSLQQRTLIYGAIMLAVIIAIVVACNMSNPLRVNPFLGMFF
>NZ_CP026729.1|WP_033501558.1|35668_35896_-|hypothetical-protein
MENKSSNGWKFFALLFGALLAGVVGLYVYKQQNPDYDPWEEPWENSSSPVDLGLTKDAEEAKEADTEAAAAPEAA
>NZ_CP026729.1|WP_154303338.1|33000_35448_+|glycogen/starch/alpha-glucan-family-phosphorylase
MTEITAPKSAVTAEQFADEIREQLKYTQGVTVEQAKPADVYVAASAAVRRHLMDSWFKTQADMVNGNTKAVGYLSAEFLMGKQLRNALLNAGLTEQFNAAVKELGFSVQDVVNAEHEPGLGNGGLGRLAACFIDSLASLGVPAFGYGIQYKYGIFEQKFDENGKQIETPDYWLTNEEPWGHIDYNRDQKVSFGGEVVEENGKKVWKPAWSVRAVPVDYMVPGYASGRVNTLRLWTAKSYDEFDLLTFNKSEYLDAVKPQVEAENISKILYPEDSTPQGKALRLEQQYFFVSASIHDAIRVFYPGQDKPDLTTFADKITFQLNDTHPVIGIPELMRVLMDEYGYDWDTAWTVTNKTFNYTCHTLLPEALEVWPSKLIGELLPRHLEIIEKIQDQFAAELKTKGVDEATIQDMAIYTGDSVRMAYLATYGGSHVNGVAELHSQLLKDVTLKNFSDVYPDKFTNVTNGVTPRRFVKLANPRLSDLITEGLGTDKWVSDLELLKGLEPLAADDEFVKKFAAVKQANKVDFANYAKREYGFDIDPNTMINTMVKRLHEYKRQALKILAVIARYADIKSGKISADNVMPRTIVFGAKAAPGYYLAKQTIQLINNVARVINNDPDVKGKLNVYFPWNYNIRLAQHLIPATDLDEQISQAGKEASGTGNMKFALNGAMTVGTLDGANVEIRERVGAENFFLFGMTVDEVDALYAEGYEPKKYYEADPRLKAAIDMVADGTFSNGDKTVYEDLVHDWLTKDWFMTLADFGAYTAIQSEIEALYAQPLEWNRKALINVANSGYFSSDRSMEDYLERIWKTGPLAD
>NZ_CP026729.1|WP_154303337.1|32207_32645_-|hypothetical-protein
MAVIREQDLHKGHDAFAQWLQTSHRIITDSIPTNTDAARDFRLEFSPRLPRQLWAMAVRYSLHLLEKKAPGEGVEVRVAPWGAIKILDGPASDPHNLTPPDVIELEPDVWMRLATGITSWQEEKDAGRITAVGERDDLSDLLPLV
>NZ_CP026729.1|WP_154303336.1|31715_32096_+|DUF3073-family-protein
MGRGRQKAKQQKIARKLKYLTTDTDYDELAKELGAQEPGSGFFDPFADIEAKYSHDADAEDEIPEDVQESTQGDAEDDLDEYAKWAAEAAAKATSGEFPAAKSAAPKPHKPIPMPMPSVLKPKKQD
>NZ_CP026729.1|WP_154303335.1|30487_31588_-|tryptophan--tRNA-ligase
MTDETQEQQITAVGNEMSASFLAAKKRSDATLAAIKQNPGKFTMLTGDRPTGRLHLGHYFGSIRERVAMQNRGVNSNIIIADYQVITDRDTTEHIEDNVLNLVLDYMAAGIDPEKTMIFTHSAVPAENQLMLPFLSLVTEAELHRNPTVKSEMEASGHALTGLLLTYPVHQACDILFCKANVVPIGKDNLPHVEITRTIARRFNERYAKKHPVFPEPAAILSEAPEIPGLDGRKMSKSYGNSIMLGATAQETAKLIKKSPTDSERRITFDPIARPQVSALLTTAGLVTGRDPKEIAEEIGDSGAGALKAYVIESVNSFLEPHRARREELAKDMDYVRDVLAEGNKKANAIANETLEQVREAMGMRY
>NZ_CP026729.1|WP_033501563.1|29520_30393_+|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein
MSDIDELHQYAIRLAQEQNSSGMIMTIEKELLHYEILNAMDEGGLLDRLVFQGGTSLRLCYGAERYSEDLDFSGGRDFDRKGLDTLKDCVEHAVGDRYHVSISVKEPRQVKSLVSAWTVIVDTTPKYKDVPRQRIKIEVASIEAHDPVIRPLKVNYEGLGDYSDIMLAVESKEEILADKIESFVCSDHVRYRDLWDLAWLSKQPGVQQNKVQDLRKQKASDYGEISKYMERYPLVQEKIANAFDSDKFVHEMSRFLPASRVNRTVAKPLWLLGTKQQLADLFIAYAPDLA
>NZ_CP026729.1|WP_033501564.1|28982_29528_+|hypothetical-protein
MKQSEAIKVLNQWDLHGRYVYLKRDLRKLFRDEPKETFDDSLSRLVKSEILVRAARGVYVYGLTRNFSDATVDLIARNLRRGYATYESLESMLSAYGVISQIPVDRRTYMTTGRSGEYQTPYGAIEFTHTARPITQTIPELLHPEGRGVPLASKQLALRDLKATHRNLDLVDYELMEETYE
>NZ_CP026729.1|WP_154303334.1|27195_28824_+|sodium/solute-symporter
MVTKDFWVLLAMVIYFVAMLTIGFIYSKRSNSSTRQYFAGGRGVGPWLTALSAEASDMSGWLLMGLPGVAYFTGAADPLWTALGLALGTYLNWKLVARRLRRYSVVAGDAITIPDFFSKRFHDKRNIVSTIAALIILVFFCVYVGSCFVTVGKLFSTLFGWDYHLTMVIGAAIVFAYTVIGGYLSVVVTDFIQGLLMFFALAVVFIGSVASVGGVDNTVAFLKGIPGFLDGTQMATPILNDAGEQIIEAGQAMFGAPTEYGVITMISMLAWGLGYFGMPQVLVRFLSIRSSEEIKKSRIIATTWCVVSLACGVCIGLVGRAMMPTQFVTQSAAENIFIVVSQALLPSFMCGIVVSGIFAASMSSSSSYLIIGASAVGENIFRGLLYRKATDRQVMMVARITLLVMFIFGIVVAFDQNSSIFQVVSYAWAGLGASFGPLMLCSLYWRRTNKFGAIAGMLSGTATVLIWHNLIKPLGGVFAIYELLPAFIISLLFIVVVSLLTPAPDAEVLHEFDHYLDDPDDRKVDDDLVAAEIASGEKRAQI
>NZ_CP026729.1|WP_033501566.1|25045_26887_+|threonine/serine-exporter-family-protein
MSAQYEHEHETNFDSAEKSASAVSKFHTHSIPLDMEDIERDWDKPVAEAGIAAKASVIVRVGMLDLGAGTGSFRVREMMHRIAYPLGVHVRADVNLTDIEASCTDGKDRITEVIDLPTTGVNTERIWLLEHFADWFNVNLGKGSMYHSQSDVSEGLMQHLDKRDASQVSADLSKRLRERQKAEQNQEGSDDPVLDALEMVTERAEATDTTAQPLHLRDIEAASEQHNRSEREAECETKRETAGTANVVASEPTTKKTRKNRNHKPPKGQYAEHFDHVGKEKNQTQGITVRQAHERLNMIERRKPLYSPAFAGFASACACASFVFLLGGGPFDMIGAFIGAGLGHWLRRRLFAHHLNQFFVTFVCVAVAALACTGTLRLIGIFEPVALQHDTAYIGAMLFVIPGFPLITGGLDMAKIDFPSGIQRVAYVLCIILMATLAGWMVASIVHLNPEGFEPLGLNPVVNCLLRFVFAFIGVWGFSTMFNSPQRMCLVAATIGAITDTLRLEIVDMGVPAEAGAFIGALLAGLLASAWRSAVHRSWLAPHLGYPRICLTVPSIVIMVPGLYMYQAMFHLGQFDTLNALDWAFRAFMVIICLPIGLAMARVITDKSWRYDI
>NZ_CP026729.1|WP_070097852.1|38979_39465_-|cell-division-protein-CrgA
MLMADEELHETTADNQNDLQSTDDTAAVEEGNETVQNAAEETTVESASADSDDDDDLDIPMDRVEAVLNATVDKDSLSPQMQRMMNRQAENTRRVEETIKGTKSNPRWFVPLFCALMIIGLVWAVVYYLTSNYPIPNIGAWNLAIAFAIIMVGFIMTMWWR
>NZ_CP026729.1|WP_033501555.1|39582_40350_+|DUF881-domain-containing-protein
MAKHTGKHTAKRSKAAGAAAVLVLMFSGFLLATNLRVNRSVVVTNDTAELVEQRVKKVNSLQAEVDALSSRVNDLSKTLSSQGDTDPQDSESAGNGTMLPAVEGPGLVVTLDDSPLWENMIDSSGSTSNINDYVVHQQDVEAVVNALWAGGAESMMIMDQRVLFNSAVRCSGNVLLLQGKKYSPPFTISAIGPVDNMKKALDDSQDVTIYRQYVSAFGLGWQVEEKEKLHFEATDALQQPLQYAQAMSDGTGETQ
>NZ_CP026729.1|WP_154303341.1|40407_41499_+|class-E-sortase
MKHVAHKQRRKSVVWTILGIFAELMLTAAAICALYIAWQMWWTGVQAEHNQIETRQSVSWSDPGQSDNVTIAQAQEGDPPTQPQSAQEGELIAQVYIPRFGSQWQRNLVEGTSLTELNKHGLGHYKDSQMPGQVGNFAFAGHRNGYGQPLGDVDKLQEGDPIIIRTQDYWYVYHYTSHKIVLPTDIEVVAANPENPGATPTKRMLTMTTCEPKYSTPTHRWISYAEFSYWAKVSDGIPQELASTDSNGKVKFVNNEKSSIVASVSSLKPWIFGALAAYVIIFLSALVAWRWPYLADVRAGRREKPEFSLYGGLMRLQPGVLPIRLVLMALLIFAAAASCFEWLFPWAATSIPALQEMSNYTAV
>NZ_CP026729.1|WP_154304349.1|41687_42332_+|C26-family-cysteine-hydrolase-domain-containing-family
MTDSARILVVDNYDSFVYTIVGYLKTLGATVTVVRNDAIDPSEAGVIDEYDGVLISPGPGAPAESGASEGMIRLCAEQSKPMFGVCLGMQALAEVFGATVSHAPTIMHGKTSLVEHIDDEIFEGVANPMTATRYHSLAVEPDSVPEELVVTAWTQSDHIVQGIKHRSKPMYAVQFHPESVMTQDGYRLLANWLKVCGQENAVERSAGLQPKVAA
>NZ_CP026729.1|WP_154303342.1|42543_44640_-|Stk1-family-PASTA-domain-containing-Ser/Thr-kinase
MNINMPTSLAGERYQLGQLVGRGGMAEVHVALDTRLGRTVAVKIMRADFANDKIFLERFRREAHSVAQMNNPNIVNIYDSGEEVVTTETGQTEHLPYLVMEYVKGQTLRDILKVNGALSQRDAEQVMMGVLNALEYSHRMGIIHRDIKPGNIMISEQGVVKVMDFGIARALDDSAATMTQSQGVVGTAQYLSPEQARGESVDMRSDLYSAGCVLYEMLTGRPPFTGDSAVAIAYQHVSEVATPPSSVVPGLPKMWDSICAKAMAKDRQNRYATASEFKNDLLTFMNGGVPMAAAFNPLTDLTNMKARKQAEMTANTVAMTPTGETAATQAFNPVTGQFEAVPNPQNGVATKTRAEQRAEAAKARKKKQIIIGSVVGGLVALLVILGVFFMLNKSDSAADMVEVPDFTATANISEARVEEQLAAKGLKLDAREDSDSSKPKGTITKQNPKGGKKVAKGSTVSVWFSTGPQSVAVPDVSNKSQDDAKSILEAAGFKVGNVRTVDNVSIEKDKVVSTDPAANSKQTEGTIITLYISSGMTKIPDNLIGQPKDSAIEQLKQAGLTQITIESEYSDSIASGAVTRVDPGVGSTVEAGTTVTIWVSTGKQQISVPSVIGMSYANAKSLLESYGFQVTVSGPEDGTVTGMSPTAGTQSDSGATITLTTKSSSTDNAGNGGGNNSNSGNNNNGNNGGNSTTPGEGN
>NZ_CP026729.1|WP_033501551.1|44636_45581_-|serine/threonine-protein-kinase
MKLIEGQLIHRRYRLDARLAQGGMGEVWKGYDIQLGRPVAIKALRGDLGVTQEAKLLRLRAEAHNSANLAHPNIAALFEYYEHDGIGFLVMEYVPSKSLADLFHEQNGPMEPTRLLPILIQTARGLFVAHSHGVIHRDVKPANIMVSDSGEVKITDFGVSYSTNQEQITQDGMVVGTAQYISPEQAQGQHATPQSDIYSLGVVAYEGLCGHRPFTGATPVDIAAAHVNNPVPPLPDSVDVQLREFVMSMLAKDPLDRPKDALTVSRTLSRIERRLLDQQTQLADTMVVPTGGRLPRRVVSRPHISLITDGKEQG
>NZ_CP026729.1|WP_154303343.1|45577_47044_-|penicillin-binding-protein-2
MNKSLRQLFTIVVALFVILGMSTTIITAIRANQLNSDPRNTRALYHEYGAPRGAILASDGSVIAKSDPSNDAFSYQRSYAAGALYAPVTGFFSISQRGWSGIEASRSSLLSGQSDQLVWQRFKSLFTGQENKGATIETSIDPKIQQAAYNGLANNDGAAVAIEVKTGRILAMASTPSYDPNQLASHDTSEANGNYSALSQNESNPMLNRVTSQLYPPGSTFKTVVAAAALETGEYQTDTEIPAGSSYTLPGTATQLTNAVSQADGSDGKITLEDAMAYSSNTAFAQLGVALGDEKISSMAEKLGFDNPIAVDGSESTGTPWVSVASNFPTDAADDKLALASIGQGDTVVTPLQNALVAAAVVNGGKVMRPTLVDRVRSSDLSVISQTKPQVMSRAFSSDTAGKLTQMMEAVVTKENQNLAIDGEQVAAKTGTAQIGNGNTSIDGWVIGFAPADDPKIAVAVVVHNVDLYGSFAAGPIMKAMMQEALAE
>NZ_CP026729.1|WP_154303344.1|47040_48666_-|FtsW/RodA/SpoVE-family-cell-cycle-protein
MMATRLKQFGLLLFSMLICGVSFFQMFERTTGGFPHNYLWMLAFVGALFLTSWGLLLRFQPYANQAIMCCVMVLTGTGIMMIARIDQDSNTSVAFKQLLWLSIALVVVNLLVIFMKDYRVLRRFSYVSMVIGLVLLLSPMLPVVGSEQYGARIWVRIPGLGSFQPSEFAKLFLAFFFASYLYDHRDQLAVGGKKVLGLQLPRIKDLGPIIVVWIVSMGVLVMQHDLGTSLMFFAMFVSMLYVATGRTSWIVIGFIAFAVGAFAAANIFSHVGARVDAWLHPFDSTQYSKEYGGSYQLVTGIFGLASGGLMGTGLGQGHPSLTPIANSDYIYAALGEELGLTGLMAILMLYLLIIAAGMITAMKIKDGFGKLLASGLVFTMAFQVFTVVGGITLVIPLTGLTLPYMAAGGSSLIANYMLAALLMVISNSANKPESDIDSDTFQYEAMQALSARKQSRARRSVSSEQSSTQSQAVSPAATQAVPQVAIPAAMQQSQATEIISTATPVAGTPIVPPAPPSNVFGTSDMPSTPNPSGNTSEGSQA
>NZ_CP026729.1|WP_033501603.1|48662_50279_-|serine/threonine-protein-phosphatase
MPTSPASQPLFMYSTVVSDVGTVRSNNQDSAFAGEHLIAICDGMGGHAGGDTASTIAIRSLAHIEQDNVQGDVQVIAHMLKTSVMAAHDAIVGKAKRERRLAGMGTTVTSVALVAGYWVVAHIGDSRAYLLHDGRLIRMTSDHSYVQHLIDTGRISESEARNHPQRNVVMRVLGDFDIDSRPDIAVRKAHPSDRWLLCSDGLCGVLEDSTLQEMLSTCSDQEECAQQLVSMALRAGSTDNVTAVIADATLALDADAFDLPHQTPLVGGAASASLEPIADIINEPVASAPALREGKKSPAARAAALRNGKNPDDNDNPPEQRVAQPSTVREENGDRTNPDTGEIPVVQKDDGRISADPNDPEVAKAIRNEHIEQRKTKRSRTRRNRVIAIIVTIVILLGLAGGAFATYRWSQTKYYIGDNNGEVSIFQGVPTSLFGFQLSHAITDTNMKTSELPPSWQEQLAQGISFDTYGEAKTHTRLIKKQLKQQQDAEAQKGQNKTNSGSDSKSSSKSSDTTSNKSSSKSGDSGNASADKSGGDQS
>NZ_CP026729.1|WP_033501548.1|50284_50800_-|FHA-domain-containing-protein
MLTELTFAILKYGFLVLLWIFVACTVRSLYRDVETLSPRKSRAHRRKERRARKAVEAPAPVAALAPVVSATSSAKPTLLVIIDGPLAGSSVPLTGNTITLGRSASNTVVLDDEFVSSHHARVYTDPATGKWAVEDLGSTNGTVVNQQRLNAPMILGTRIPVRIGATTFELR

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Crispr_ID: NZ_CP026729_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_2

62170-62267

Orphan

Consensus_repeat	Method
AATCGAATAACGGTAATCCGTTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP026729_2

>merge|NZ_CP026729|2|62170-62267|CRISPRCasFinder
AATCGAATAACGGTAATCCGTTCATGAAGCCCACGGCGCAAGGCGGTGCCAACGTGCCGCCGGCCGGGTCGAATAATCCGAATAACGGTAATCCGTTC

>NZ_CP026729|2|2|62170-62267|CRISPRCasFinder
AATCGAATAACGGTAATCCGTTC	ATGAAGCCCACGGCGCAAGGCGGTGCCAACGTGCCGCCGGCCGGGTCGAATA
ATCCGAATAACGGTAATCCGTTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154303346.1\|55771_56428_-\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP026729.1\|WP_081962282.1\|74888_77213_-\|YhgE/Pip-domain-containing-protein	unknown	unknown	gnl\|CDD\|224428
NZ_CP026729.1\|WP_154303358.1\|69349_70804_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|215457
NZ_CP026729.1\|WP_154303348.1\|56718_57798_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|378820
NZ_CP026729.1\|WP_033501548.1\|50284_50800_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|238017
NZ_CP026729.1\|WP_154303359.1\|70997_72098_+\|zinc-metalloprotease-HtpX	unknown	unknown	gnl\|CDD\|235102
NZ_CP026729.1\|WP_154303347.1\|56435_56597_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154303357.1\|66438_67449_-\|asparaginase	unknown	unknown	gnl\|CDD\|199207
NZ_CP026729.1\|WP_033524162.1\|80223_81291_+\|class-II-fructose-bisphosphate-aldolase	unknown	unknown	gnl\|CDD\|236406
NZ_CP026729.1\|WP_154303345.1\|51747_54195_+\|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl\|CDD\|366030
NZ_CP026729.1\|WP_154303351.1\|59012_59240_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|334619
NZ_CP026729.1\|WP_154304350.1\|54516_55689_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|226951
NZ_CP026729.1\|WP_154303363.1\|77215_79915_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224428
NZ_CP026729.1\|WP_154303356.1\|63961_66397_+\|heavy-metal-translocating-P-type-ATPase	unknown	unknown	gnl\|CDD\|319844
NZ_CP026729.1\|WP_033501547.1\|50827_51535_-\|DUF3662-and-FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|378850
NZ_CP026729.1\|WP_154304351.1\|67593_69081_-\|amino-acid-permease	unknown	unknown	gnl\|CDD\|224038
NZ_CP026729.1\|WP_154303361.1\|72489_73722_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP026729.1\|WP_154303353.1\|59784_61152_-\|tRNA-guanosine(34)-transglycosylase-Tgt	unknown	unknown	gnl\|CDD\|234642
NZ_CP026729.1\|WP_154303350.1\|57896_58868_+\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP026729.1\|WP_154303362.1\|73789_74746_+\|aromatic-amino-acid-DMT-transporter-YddG	unknown	unknown	gnl\|CDD\|183277

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154303346.1\|55771_56428_-\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	3.00041e-34
NZ_CP026729.1\|WP_081962282.1\|74888_77213_-\|YhgE/Pip-domain-containing-protein	gnl\|CDD\|224428	COG1511, COG1511, Predicted membrane protein [Function unknown].	2.46924e-92
NZ_CP026729.1\|WP_154303348.1\|56718_57798_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|378820	pfam12146, Hydrolase_4, Serine aminopeptidase, S33. This domain is found in bacteria and eukaryotes and is approximately 110 amino acids in length. It is found in association with pfam00561. The majority of the members in this family carry the exopeptidase active-site residues of Ser-122, Asp-239 and His-269 as in UniProtKB:Q7ZWC2.	3.03536e-38
NZ_CP026729.1\|WP_033501548.1\|50284_50800_-\|FHA-domain-containing-protein	gnl\|CDD\|238017	cd00060, FHA, Forkhead associated domain (FHA); found in eukaryotic and prokaryotic proteins. Putative nuclear signalling domain. FHA domains may bind phosphothreonine, phosphoserine and sometimes phosphotyrosine. In eukaryotes, many FHA domain-containing proteins localize to the nucleus, where they participate in establishing or maintaining cell cycle checkpoints, DNA repair, or transcriptional regulation. Members of the FHA family include: Dun1, Rad53, Cds1, Mek1, KAPP(kinase-associated protein phosphatase),and Ki-67 (a human nuclear protein related to cell proliferation).	2.00253e-17
NZ_CP026729.1\|WP_154303359.1\|70997_72098_+\|zinc-metalloprotease-HtpX	gnl\|CDD\|235102	PRK03072, PRK03072, heat shock protein HtpX; Provisional.	1.04974e-177
NZ_CP026729.1\|WP_154303358.1\|69349_70804_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|215457	PLN02852, PLN02852, ferredoxin-NADP+ reductase.	2.19762e-106
NZ_CP026729.1\|WP_154303357.1\|66438_67449_-\|asparaginase	gnl\|CDD\|199207	cd08963, L-asparaginase_I, Type I (cytosolic) bacterial L-asparaginase. Asparaginases (amidohydrolases, E.C. 3.5.1.1) are enzymes that catalyze the hydrolysis of asparagine to aspartic acid and ammonia. In bacteria, there are two classes of amidohydrolases. This model represents type I L-asparaginases, which are highly specific for asparagine and localized in the cytosol. Type I L-asparaginase acts as a dimer. A conserved threonine residue is thought to supply the nucleophile hydroxy-group that attacks the amide bond. Many bacterial L-asparaginases have both L-asparagine and L-glutamine hydrolysis activities, to a different degree, and some of them are annotated as asparaginase/glutaminase. One example of an enzyme with no L-glutaminase activity is the type I L-asparaginase from Wolinella succinogenes.	4.38429e-115
NZ_CP026729.1\|WP_033524162.1\|80223_81291_+\|class-II-fructose-bisphosphate-aldolase	gnl\|CDD\|236406	PRK09197, PRK09197, fructose-bisphosphate aldolase; Provisional.	0
NZ_CP026729.1\|WP_154303345.1\|51747_54195_+\|prolyl-oligopeptidase-family-serine-peptidase	gnl\|CDD\|366030	pfam00326, Peptidase_S9, Prolyl oligopeptidase family.	5.42245e-44
NZ_CP026729.1\|WP_154303351.1\|59012_59240_+\|hypothetical-protein	gnl\|CDD\|334619	pfam01638, HxlR, HxlR-like helix-turn-helix. HxlR, a member of this family, is a DNA-binding protein that acts as a positive regulator of the formaldehyde-inducible hxlAB operon in Bacillus subtilis.	1.49838e-09
NZ_CP026729.1\|WP_154304350.1\|54516_55689_-\|ATP-binding-protein	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.41971e-08
NZ_CP026729.1\|WP_154303363.1\|77215_79915_-\|ABC-transporter-permease	gnl\|CDD\|224428	COG1511, COG1511, Predicted membrane protein [Function unknown].	6.00156e-101
NZ_CP026729.1\|WP_154303356.1\|63961_66397_+\|heavy-metal-translocating-P-type-ATPase	gnl\|CDD\|319844	cd07544, 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_CP026729.1\|WP_033501547.1\|50827_51535_-\|DUF3662-and-FHA-domain-containing-protein	gnl\|CDD\|378850	pfam12401, DUF3662, Protein of unknown function (DUF2662). This domain family is found in bacteria, and is approximately 120 amino acids in length. The family is found in association with pfam00498.	4.03141e-41
NZ_CP026729.1\|WP_154304351.1\|67593_69081_-\|amino-acid-permease	gnl\|CDD\|224038	COG1113, AnsP, Gamma-aminobutyrate permease and related permeases [Amino acid transport and metabolism].	1.11987e-173
NZ_CP026729.1\|WP_154303361.1\|72489_73722_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	6.10297e-16
NZ_CP026729.1\|WP_154303353.1\|59784_61152_-\|tRNA-guanosine(34)-transglycosylase-Tgt	gnl\|CDD\|234642	PRK00112, tgt, queuine tRNA-ribosyltransferase; Provisional.	9.51472e-166
NZ_CP026729.1\|WP_154303350.1\|57896_58868_+\|EamA-family-transporter	gnl\|CDD\|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	4.00419e-24
NZ_CP026729.1\|WP_154303362.1\|73789_74746_+\|aromatic-amino-acid-DMT-transporter-YddG	gnl\|CDD\|183277	PRK11689, PRK11689, aromatic amino acid efflux DMT transporter YddG.	1.4499e-127

>NZ_CP026729.1|WP_154303353.1|59784_61152_-|tRNA-guanosine(34)-transglycosylase-Tgt
MTSLIESSTDTAQDTQNAATAVSENLIEHPRGAEPGKPGRRDAFYFEQKTRLPDAADGKGRGGARYGRTGTIHTPHGDIHTPAFVPVATQAAMKAVLPETMKDLGAQCLLSNAFHLYERPGEQVLDEAGGLAKFMNWNGPTFTDSGGFQVLSLGAGFKKTLAMDVTGMKSDDVIAEGKERLAFVDEDGVTFKSPLNGSLHRFSAEISMGIQHKIGADIMFAFDELTTLMNTRGYQVRSVERTYRWAQRCVAEHKRLTEERVGKPYQALYGVVQGANYEDLRRHAAEQIASLDFDGVGIGGAIEKRIIGDTCAWICDAMPESRPRHVLGIAAVDDIFACVENGGDTFDCVAPARCGRNGAIFTRDGRYNIKRAQFKHDFGPLEEGCDCYTCTHYSRAYVDHALRAREFNGFTLATIHNEHFFVKLLDDIRASIDGGYFDEFRNEALARFYTNGSRG
>NZ_CP026729.1|WP_154303351.1|59012_59240_+|hypothetical-protein
MLRTSDHDKAHVGAGEHVGQMLGSVRDCRQSLFGPSADRVHDHVEYSLTEVGESLRPIIEAMKTWGNHYRDEHES
>NZ_CP026729.1|WP_154303350.1|57896_58868_+|EamA-family-transporter
MAKQTSGQTSQSQKTSESQKTAKKTEHVLEQTPKSLLIGTGMTLLGGAMWGMNSTMAKLLMRDYQLDPIWLSCVRALFASLIFLVGSAITTPQKLAGAVKDVKSYPKYLVTTLICVLLVQVSYLMTIDWTNSGTATVLQTLNLIFVLAWVCLRGRRLPLKRELVGVLLAFAGTFLIATGGNFASLSLPWQGLAWGLIDAVSTAAMSILPVMLMLKWGNMTINGITFLMSGLILCPFAQPWVNIPALDARGMLLLLYTIVCGTFLAFWLYMAGVMRVGAVRATMLGTSEPVMATITAVAWAGETFTFTDLTGFAMIIIMVFLVR
>NZ_CP026729.1|WP_154303348.1|56718_57798_+|alpha/beta-fold-hydrolase
MEFMTITLIDEARYDAEMDETVLPALRNCMTEGWMEPTTIDWDGNMLPKLKHPGRLHYYCYDAHKFDALREDGASGVFRGAVVISHGFTEFGRKYSEMVWYFLLAGYSVCVFEHRGHGHSTHDMSNPSLVWIDDWHRYVADFATFAQTVGREVAGDGPMYLYCHSMGGGIGAAVLERYPSLFDKAVLSTPMIAPVVGMPTWIARIVVGVICGLGFGKSRVFGHTDFDGNLNPDDYKGASEARIRWFHKQRLTDKSCQTNAATFDWANQAMALSRAVLKPDMCGAIEAPVLLFQAGRDVWVLNGPQDDFVERVREGGGSIEKVRYSQSLHEIFSMPNAVLESYLDKILVFLAAPNASLAE
>NZ_CP026729.1|WP_154303347.1|56435_56597_-|hypothetical-protein
MKCVSLLMVVTLSLTSTPAYAYAATPVNGNDDISTAANPNCPTWLQWLCGKGK
>NZ_CP026729.1|WP_154303346.1|55771_56428_-|response-regulator
MTTSEKHPKIHRIALVDNDPRALDSLSAVIACKVPTAYVVWTATSGDEAIERCQDANSNVSLLILDMSMEGLQGPATCRRLRLMGKHMPILGATSFSIKSYRDKLVEAGAQGLVGKENADQLAQIIMRMCDGEVMEGFETPALANLRISREAETAPSLTVREEQIISLCAEGMLDREIAERLGISEATIRKHMQSILRKLNCKTSRQAVALWVRSNAF
>NZ_CP026729.1|WP_154304350.1|54516_55689_-|ATP-binding-protein
MLIVLIWTVYGVCYEPPTDISGMVWIAMLVAALVVSPLFPKSMSVAIIVIVYAGDLFTSYASSGNSLPTHLYAYGMLAYSTNVIIAAALFTYYIATILLISPPGPGTNPVSMISMYAMVLLLGRALSWSEKTTRKRFEAAQNKNRLQELESRARIADAIHDAVTGDLSAAAFVAQRHVDGVSGSPSAAAGGPASAADAADAEDWRQINEYILFALTNVHRVIDELNMDATVLPGDADGEALANLLQATMNDGDRRLRKLGFEITSIRHCAGGKPSASRETAELANNLLREIYANIARHAAPVSKVDLSVMLRPNAIEITQINPMKEGIAGADGHDNELPGGHGLASFKKQLESHQGTLTASAQDGSWTLFAYIPVTVIDDSPGLFEQVQA
>NZ_CP026729.1|WP_154303345.1|51747_54195_+|prolyl-oligopeptidase-family-serine-peptidase
MTDAIRQFPRKKARTLRFSCGAPRSARVIADGSRALFLRSDGSEDTVTSLWMSVIDENGNASEMLLADPRTLLADADAEDVPAEERARRERAREGGSGIVGYSTDVSGNRVTFTINGQLFLTDIAAGVTRAIAIEEDELKPVLNPRISPDGQHVMYTTGTYLVNVDLADTAFDTASGDDDCEIGDAISVVASIPQDGEWKIGLAEFAAGEEMDRYDGFWWSPDSKYVLFETYDESPEPIWHLSDPANPANPARSNRYPQALTANANVRLTLLELGFDSDNCCYGAIANEVQWDHETYEYLAAVSWTSGHEPIILVQDRRQQHDQVLAIHVGEPIATMRDAENGFTDDEGDQVETFSIAIPEYAEGERPGSTRVLEEHSNAYWLDLIHGTPAFTPNGRLICAMNDMDADTNRLTANGVPFTPAGLQVREVLDVTDDDVLCVVQRTPELLPDDSLPFLWQSNAADHDARSFDVVSIRYDGTWEPLTYAPGQWAISRAGNGCVVTGRGMDDATVQMQHCMNIATTDENGTDVASMVVAPIENHAETPGFTPNVHFTRLGERGLYTAIVLPSASSEYAHADTLPVLMKPYGGPGFQQVVESQSFYWDAQWWADQGYIVVTADGRGTTGRGPKWDRAIYETMKSVTLEDQVDAVRALPEALATLAVQENKESSETTIPQPDLNRVAMIGWSYGGFLSALAVLEEPETFAAACAGAPPTDWTLYDTHYTERYLGLDPAVYERNSIISDAPQLDRPLMLIHGFADDNVTIAHSLRLSQALMAAGRKHTFLPLTGITHMTNDETVAENLLILQRDFLAEALER
>NZ_CP026729.1|WP_033501547.1|50827_51535_-|DUF3662-and-FHA-domain-containing-protein
MSVLDRFEKSVEGAVNGVFAKFGSKDLQPVDLSSALEREIDKEAMPVTRDRTVAPNEYRFKLSTPDFNNIVDWGAEALANELADNLTQYAKDQHYAFVGPVVVIFEEDLELTKSNFKLTSESVQGNTVPVTTEAQTEDCPMLEIGEHQYLLTESKTIIGRGSDCDIVIDDPGISRRHMEIDVTDNGSTVIARDLGSTNGMYVEGHHVEAATLLDGNTITIGRTRILYWASSQDQE
>NZ_CP026729.1|WP_033501548.1|50284_50800_-|FHA-domain-containing-protein
MLTELTFAILKYGFLVLLWIFVACTVRSLYRDVETLSPRKSRAHRRKERRARKAVEAPAPVAALAPVVSATSSAKPTLLVIIDGPLAGSSVPLTGNTITLGRSASNTVVLDDEFVSSHHARVYTDPATGKWAVEDLGSTNGTVVNQQRLNAPMILGTRIPVRIGATTFELR
>NZ_CP026729.1|WP_154303356.1|63961_66397_+|heavy-metal-translocating-P-type-ATPase
MRRIIDICWRLCKQVPLLPITILSAIPLALLGEWRPWGEAAWVSHDLHAGFGWLNAFNPGVGQWIVIVLVAYTIVVTVRGMIDDLRNGHVGVDLLAVVAIASTVAVQEYWAAWAVVLMISSGEAIEEFAQSKAESNLTALIDAAPRTAHVVALPGVRGHVHATGSEHTADVTADGFRAVRMSDSAETDNQDGEKHTYVSESPESDTKGTSQTYDAAGECFETVPVDQVRLGDVILVLPGETVPVDGELLSGVATLDLSNINGEPVPREVYAGARVMSGAVNGSSTLTMRATQLAQDSQYQKILELVSSAQESRPAVVKTADMLAVPFTVLSLAIAGIAWAVSGLPLRFAQVLVLATPCPLLIAAPVAYVAGTGRLAKAGILIKAQDVLENLGRVSHIFFDKTGTLTVKQPQVVRVEKPFETSSPLNEDHILMMAGVVESYSVHILSKGIAAAGRKAMGDLYARYTSGQRLCAERDLPGHGHDYPVVKNIVEDSGKGVAGEVNGHRVRVGRFAYVTADEAGFMPVLHAPGERYVSDSPKSDTLGVRDGMSDDAQSTVVAPSITSYAEASQTTPVRKSETANSLFAPLAPDEMAAYVAIDGKLAARIVLRDVPRANTKRSLARLHELGIKELSMLTGDKAASARIIANEVGIDDVQSELFPEDKVAAVKNATESTHQNQSMPARIMRRITGESRNHQVTMMVGDGVNDAPVLAVADIGMAMTDGTSTAASESAQVVIMNDDIASVPRAIAIARRTKNVMLQAVLIGLGLAIIGMVAAAFNLIPVVVGAFMQEVIDVVSILWALTVLFDRGESA
>NZ_CP026729.1|WP_154303357.1|66438_67449_-|asparaginase
MRIHITYTGGTIGMIDSPNGLIPGADTRGWLFRLLEDAHMDASLFTFTELDPLIDSSNATPDNWQTMVDDLRAHHDDADAFVVLHGTDTMSYSSAALSYALADFGKPVIFTGSQHPLGKIESDATANVTGALNAAMSGRFHGVGLFFGHHLFAGNRVSKSSSWAFEGFSAPSVGPLARTGTPWHWYAGDSAAVGCGWTSPQPYSRHDVAVIDMAPGISAARLEAMLTPRPEAVLLRAYGVGNVPSDEPGLTDVIADVLHDDVPVVIASQCQQAEVLLGHYETGDAIARAGAIGSGDMTLEAAYAKIMFLLSQGVTGADFGKWMRVSIAGEISPSSL
>NZ_CP026729.1|WP_154304351.1|67593_69081_-|amino-acid-permease
MAQSKAPEQGGVRKLDKSDAGYAKDLKPRHIQMIAIGGSIGTGLFLGAGGRLAQGGAGLAIAYAVCGIFAFLMVRALGELAIRRPSSGAFVSYAREFLGEKGAYVTGWLFFLDWSVTVMADITAVAVYFHYWKAFQGVPQWLLALIALALVFVLNLLSVKMFGEAEFWFAAIKVATIIAFMVIAIWAIVTGAPVGGSHAGVANITDNGGLFPKGIAPVFALTLGVVFAFGGTEMVGVAAGEAKDAEKVLPKAINSMIIRIFVFYVGSVVLMTLVLPYTAYSSNESPFVTFFSGIGIPHAGDVIQVVVLTAALSSLNAGLYSTGRTLRSLAVAGSGPKFAARMNKHHVPYGGIIITSALGLIGVVLNAVLPSDAFEIVMNLAGIGIAGTWAAILVTHISFLKKVKAGEETRPAYRMPGAPYTNYISLLFFAVVVLSNLTSAAGRWTLLMFAVVVVAMIAGWFYVRGRINGNLMDEMLDDNDNDVADVLETTEVPGK
>NZ_CP026729.1|WP_154303358.1|69349_70804_+|FAD-dependent-oxidoreductase
MTETNELRIAVIGAGPAGVYSSDIFLRQLKKLGEGLGLGTAARIDLFEKLPVPFGLVRYGVAPDHPSIKFIASALEKTLDNPDIHLYCDVEFGKDVTLDELLERYDAVLFATGAVEDKPLGLPGADLDGVYGAAKFVEWYDGYPTGAREWPLEAEEVAVIGGGNVAMDVARELMRNADDLKERTDIPDNVYEGVKANKARVLHLFIRRGVAQAKFSVQELREMEKLPGVQLIINEDDFDLDEDTIEEAGKDKLTRQMVEELFTIREMAEDMEDDGDVDYEGNTADRKYYVHFNSAPVEVLGEDGKVVGIRVEKTETSADGKMSRTGEFEEYPVQAVYHAIGYKPATAPGIAYDERHAHLANANGDGRITTTASAEDGAQVRERLYATGWAKRGPVGLIGSTKSDALLIVTNMLEDLSKAAEGGRVADDRDPESIDRLLASRGVKPIDFAGWKKIDAFERAEGAKEGREHKKVIDPEQMRALAHA
>NZ_CP026729.1|WP_154303359.1|70997_72098_+|zinc-metalloprotease-HtpX
MNGKLQVHGHCNGLKTTLLFALMWGVIMLIWWATGGSQRTLGIYILIGLGSTFASYWFSDKLAIASMRAQEVSEQEAPVLYKIVRELSAKAGKPMPRIYIAPTMSPNAFATGRNERHAAVCCTQGILQMLNEREIRGVLGHELMHVYNHDILTSAIASAMATVISYLGYSLMYFGGGNSRDDRNDSSSNGLGLLGVLLSTILAPIAASLIQMAISRTREYDADEDGSMLTEDPEALASALNKISNGAETMPMQKTAGTQSVAAMMIANPFSAEGFSKLFSTHPPTSDRIARLMQMGQEMRQQGVQSGYLAGGYATSGVAAADIRQGGRSAMAGAGGPQFGTQYGSGHDSVGSAGGSFRDYSQRPRG
>NZ_CP026729.1|WP_154303361.1|72489_73722_+|helix-turn-helix-domain-containing-protein
MSFKENLQYLRGSRNMTQKQLAMLLGVSRQAISKWESEKAYPEMDKLLMLCDMFGVTLDDLVMGDVRASAGCGGARRVDLAADTDGVAASVGVADAAVGAVPGVIGFAASQVAGMSDSGESDAQGAKTGVQLSVSPESDTRDGADIPQSVPRHIVQDVVGYDSHMRRFAWLIAIGVAAIILGVAVGMLFSPEGSVLGPSPVNDVLVTVCTLVGAMVGLALLIPAGIMHGDFRRRHPYVQDFYTNEDKSRASVVLAIGVAIGAVLILAGVCVRVFCDEFVADGDAGWPDSVLLACVAAAVFCFIMSGMTHDKVNVDKYNREAEEESVREGRSVPHPTMSESDRFYSRLTGAICGVIMLLATVVALLMLFLGTAGSDADTWMKVFWVPWPIGGVLCGVVGIIVPLVKEARRR
>NZ_CP026729.1|WP_154303362.1|73789_74746_+|aromatic-amino-acid-DMT-transporter-YddG
MNTDQKLPAESAGERPSNPLFGHAISHAATLIGLFAIVLWGFMAGLVRLVSESFGATLGSALIYTVGGMLLLIVRRPKPISQAPRKYLVAGGLMFIAYEASISLSIGLATTNAQSVEVSLVNYLWPTLLVLMTAAVSHKRGSVSEALPGAIVATVGVAMAVGGENLDVQEAVANIASNPLPYVLAFAGAFIWAIYATVTPSMSDGYDGTTIFFCCVAVVLWIIHFVSGDGLPAVAPGIGGYIALLACAASIAGGYACWGYGMLHGSMETLAIGSYATPLFSTASSTLLLGVTLGMPFWIGVALVVVGSLINVWFARRC
>NZ_CP026729.1|WP_081962282.1|74888_77213_-|YhgE/Pip-domain-containing-protein
MIWGIFKRDMCHATRNVIAVIVSMGLVVVPALYAWFNIAASWDPYGNTKALKVAVANNDKGYKSDLIPVRVNVGETIISTLHANDQLDWQFVKSDKAIDGVKSGEYYAAIVIPKGFSADMMTLFSPDIKHAQLKYYLNEKINPIAPHITDQGATTVVNTIDKTFAKTIAQVGLDLASSILRYSQSPQMAEYMRNLNGNLTTMADTLSGASQQVTSYSQLLGSANDIVDSTGKLLASATTAGKQAQNALKQGKSGATSFTSAGANVTSSVNTALDQVLGAFDQVAAKVNKAFDAIGKGADTAASQLTTLSEQVSSGESLYDTYITSLNHMRESVEQLPDSDSAKQALLEAIDREITLLEAAKGDSQKLAQQLKDASTQVTQDAAAAESSRKEILNRITSAKQSISNVRDDYATNVKPKIDALASTVSTLISQTDSMITQLSGTADDLDDVTGDVGTNVTSIRSALGAIAKKLDSSAATVKELITKLETGGNAGDGNSDGGDGDNDASSSDSGESDELRALATANASTLSTLISAPVALHRVSVYPIANYGSAMAPFYTILSIWVGAIILCAMLKVTISDREKAHVLGLGDTLPRIAGPSGPGNASRWGLRLDHEYFGRYTIFALLALLQGTLVCLGDMYFLGVQANHALQFLAVGWLAALVFSNIVYTLTVSFGDIGKAVAVVLLVMQVAGSGGTFPIETLPKFFQMLYPFLPFPHAIDAMHAAMAGSYGNEYLLDMVYLALFLIPSLLLGLVLRKPVIRLNNWVSRNLESTKVM
>NZ_CP026729.1|WP_154303363.1|77215_79915_-|ABC-transporter-permease
MHQVFAIFLRDVKRILKNPVALVVTLGVAIIPSLYAWCNILANWDPYANTGNIQVAVANEDKGTTSTLVGHLDAGQQTVNQLKKNHQLGWRFVPKQQAIEGVESGKYYAAIVLPEDFSSRLIGTVTGKGDRPSITYYINEKLNAIAPKITDTGATTIDEQINTTFVSSVADAVAEEVKEAAGETTGSVKSAQSDVINDLTDTINQLETVQQQLRDTRSTLDKALTTIDSAKQSNIALASEITNSLDTVGKASDLLSETRTQTERFSNTLVGALDNGSTQLSGLQVNVSNATGTVLSGLNTTQDALDQVSSTMHHVNTTTDNVLDSVEKALQASQLDPNSQTYKDLSAQLAEARKQLTFQQQRIDAFDQDTTAAINAGKNTANGFNDDVTTLAKNGTASMASARTTITGTVMPNLNTGLDTLSLANGSLSGTLTTLQSTLEQGNGLLDQLSRTVTQTNTTIAGTQTQLANLAKQLNTTRTDVAALSSSAMFQQLSQALGLDASEVGSFVGEPVHLDEQVLYPVKNYGSAVTPFYTNLALWVGGFVLVAIYKLEVDRDEKIRMYTPRQGYMGRWLLFVTVGFLQAIIATIGDLALGIQCEHPFLFILVGIFASFVYVNIIYALAVAFRHIGKAVAVILVIIQIPGAAGLYPIEMMPEFFRRLKPFLPFTYGINAMRGPIGGMYANHYWIDMLSLFWYLPVALFIGLVVRKLALNLNRLFDNRLADTDLMITEHNEGTVEPLRLTETAKQIAEEFPELARRRAIHFFRMYPRLVRWGFLALAVLPFVFLLLLFITRMKLAMLLGWIISIIAIDTYLIVVEYLRERYANYLGEEAMSAEEFRSAILHENLLFRPGMHYKPMHAIRTRLYEAAHGGSAGHAAEYAAGNTDGNAGRSRREEGSEQ
>NZ_CP026729.1|WP_033524162.1|80223_81291_+|class-II-fructose-bisphosphate-aldolase
MTIATPERYAQMLDAARRGGYAYPAINVTSTQTLNAALQGFAEAESDGIIQVSVGGAAYFSGQRVNDRVTGSLAFAAFAHEVAAKYPNITIALHTDHCAKQYLDEWVRPLLDHEVEQVKHGQEPTFQSHMWDGSTVPLGENLDIAEELLDKSQAAHTVLEIEIGAVGGEEDGHSAEINDKLYSTPAQGIAVAQRLGLGERGRYMAAFTFGNVHGAYKPGVVKLRPELLDEIQTTVALAIKAGEMPDPAHSLDVASGKPFALVFHGGSGSAPEEIAQAVSYGVVKMNIDTDTQYAFSRAVAGHMFSNYDSVLKIDGEVGNKKMYDPRSWGREAESAMAARVVEACRQLGSAGKALK

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Crispr_ID: NZ_CP026729_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_3

482857-482933

Orphan

Consensus_repeat	Method
AGTCACTGGAATAATCTCCCCGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP026729_3

>merge|NZ_CP026729|3|482857-482933|CRISPRCasFinder
AGTCACTGGAATAATCTCCCCGCTAGGGAGCGCGTGAGAGTCCGTATTCTTCTAGTCACTGGAACAATCTCCCCGCT

>NZ_CP026729|3|3|482857-482933|CRISPRCasFinder
AGTCACTGGAATAATCTCCCCGCT	AGGGAGCGCGTGAGAGTCCGTATTCTTCT
AGTCACTGGAACAATCTCCCCGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154303521.1\|484308_485310_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238919
NZ_CP026729.1\|WP_154303520.1\|483202_484255_+\|ADP-ribosylglycohydrolase	unknown	unknown	gnl\|CDD\|377122
NZ_CP026729.1\|WP_004268639.1\|472248_472338_+\|AURKAIP1/COX24-domain-containing-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154303517.1\|479156_480023_+\|PRD-domain-containing-protein	unknown	unknown	gnl\|CDD\|170086
NZ_CP026729.1\|WP_033500862.1\|486924_487485_+\|cysteine-hydrolase	unknown	unknown	gnl\|CDD\|376404
NZ_CP026729.1\|WP_154303519.1\|481304_482591_+\|serine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235461
NZ_CP026729.1\|WP_033500853.1\|473428_474709_-\|ribonuclease-H	unknown	unknown	gnl\|CDD\|260010
NZ_CP026729.1\|WP_154303516.1\|477041_479129_+\|PTS-transporter-subunit-EIIC	unknown	unknown	gnl\|CDD\|273919
NZ_CP026729.1\|WP_154303526.1\|493549_495718_-\|DUF4037-domain-containing-protein	unknown	unknown	gnl\|CDD\|379078
NZ_CP026729.1\|WP_003835555.1\|487703_488390_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP026729.1\|WP_154303518.1\|480062_481184_-\|diacylglycerol-kinase	unknown	unknown	gnl\|CDD\|224513
NZ_CP026729.1\|WP_154303514.1\|471419_472046_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154303524.1\|492041_492617_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_033500861.1\|485425_486877_+\|allantoin-permease	unknown	unknown	gnl\|CDD\|271377
NZ_CP026729.1\|WP_154303522.1\|488386_490003_-\|PspC-domain-containing-protein	unknown	unknown	gnl\|CDD\|226951
NZ_CP026729.1\|WP_154303525.1\|492831_493479_-\|DUF4125-family-protein	unknown	unknown	gnl\|CDD\|379239
NZ_CP026729.1\|WP_154303523.1\|490116_492039_+\|PspC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377200
NZ_CP026729.1\|WP_154303515.1\|475042_476719_-\|alpha-D-glucose-phosphate-specific-phosphoglucomutase	unknown	unknown	gnl\|CDD\|100094
NZ_CP026729.1\|WP_157872354.1\|474782_474953_-\|GHKL-domain-containing-protein	unknown	unknown	gnl\|CDD\|379627
NZ_CP026729.1\|WP_033500852.1\|472555_473254_-\|ribose-5-phosphate-isomerase-RpiA	unknown	unknown	gnl\|CDD\|234816

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154303521.1\|484308_485310_+\|hypothetical-protein	gnl\|CDD\|238919	cd01944, YegV_kinase_like, YegV-like sugar kinase. Found only in bacteria, YegV-like kinase is part of the ribokinase/pfkB sugar kinase superfamily. Its oligomerization state is unknown at this time.	6.61761e-84
NZ_CP026729.1\|WP_154303520.1\|483202_484255_+\|ADP-ribosylglycohydrolase	gnl\|CDD\|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	4.85735e-53
NZ_CP026729.1\|WP_154303517.1\|479156_480023_+\|PRD-domain-containing-protein	gnl\|CDD\|170086	PRK09772, PRK09772, transcriptional antiterminator BglG; Provisional.	1.92505e-43
NZ_CP026729.1\|WP_154303519.1\|481304_482591_+\|serine--tRNA-ligase	gnl\|CDD\|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP026729.1\|WP_033500853.1\|473428_474709_-\|ribonuclease-H	gnl\|CDD\|260010	cd09278, RNase_HI_prokaryote_like, RNase HI family found mainly in prokaryotes. Ribonuclease H (RNase H) is classified into two evolutionarily unrelated families, type 1 (prokaryotic RNase HI, eukaryotic RNase H1 and viral RNase H) and type 2 (prokaryotic RNase HII and HIII, and eukaryotic RNase H2). RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner. RNase H is involved in DNA replication, repair and transcription. RNase H is widely present in various organisms, including bacteria, archaea and eukaryotes and 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 (DEDD), residues and have the same catalytic mechanism and functions in cells. One of the important functions of RNase H is to remove Okazaki fragments during DNA replication. Prokaryotic RNase H varies greatly in domain structures and substrate specificities. Prokaryotes and some single-cell eukaryotes do not require RNase H for viability.	4.25162e-61
NZ_CP026729.1\|WP_154303516.1\|477041_479129_+\|PTS-transporter-subunit-EIIC	gnl\|CDD\|273919	TIGR01995, beta-glucosides_PTS_EIIBCA, PTS system, beta-glucoside-specific IIABC component. This model represents a family of PTS enzyme II proteins in which all three domains are found in the same polypeptide chain and which appear to have a broad specificity for beta-glucosides including salicin (beta-D-glucose-1-salicylate) and arbutin (Hydroquinone-O-beta-D-glucopyranoside). These are distinct from the closely related sucrose-specific and trehalose-specific PTS transporters.	5.46781e-136
NZ_CP026729.1\|WP_154303526.1\|493549_495718_-\|DUF4037-domain-containing-protein	gnl\|CDD\|379078	pfam13228, DUF4037, Domain of unknown function (DUF4037). This presumed domain is functionally uncharacterized. This domain family is found in bacteria and eukaryotes, and is approximately 100 amino acids in length. There is a single completely conserved residue P that may be functionally important.	6.28735e-32
NZ_CP026729.1\|WP_003835555.1\|487703_488390_-\|response-regulator-transcription-factor	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	6.76121e-61
NZ_CP026729.1\|WP_154303518.1\|480062_481184_-\|diacylglycerol-kinase	gnl\|CDD\|224513	COG1597, LCB5, Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase [Lipid metabolism / General function prediction only].	5.83915e-41
NZ_CP026729.1\|WP_033500861.1\|485425_486877_+\|allantoin-permease	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).	2.80553e-35
NZ_CP026729.1\|WP_033500862.1\|486924_487485_+\|cysteine-hydrolase	gnl\|CDD\|376404	pfam00857, Isochorismatase, Isochorismatase family. This family are hydrolase enzymes.	2.08842e-24
NZ_CP026729.1\|WP_154303522.1\|488386_490003_-\|PspC-domain-containing-protein	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.04968e-21
NZ_CP026729.1\|WP_154303525.1\|492831_493479_-\|DUF4125-family-protein	gnl\|CDD\|379239	pfam13526, DUF4125, Protein of unknown function (DUF4125).	6.01254e-102
NZ_CP026729.1\|WP_154303523.1\|490116_492039_+\|PspC-domain-containing-protein	gnl\|CDD\|377200	pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.	3.38958e-17
NZ_CP026729.1\|WP_154303515.1\|475042_476719_-\|alpha-D-glucose-phosphate-specific-phosphoglucomutase	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_CP026729.1\|WP_157872354.1\|474782_474953_-\|GHKL-domain-containing-protein	gnl\|CDD\|379627	pfam14501, HATPase_c_5, GHKL domain. This family represents the structurally related ATPase domains of histidine kinase, DNA gyrase B and HSP90.	5.87929e-09
NZ_CP026729.1\|WP_033500852.1\|472555_473254_-\|ribose-5-phosphate-isomerase-RpiA	gnl\|CDD\|234816	PRK00702, PRK00702, ribose-5-phosphate isomerase RpiA.	7.24143e-122

>NZ_CP026729.1|WP_154303519.1|481304_482591_+|serine--tRNA-ligase
MLDIQFIREHADVVKESQRKRGESVELVDEVLRSDEVRRSSLKEFEAARAQQKEIGKKVAAAQADEKAKLIAETKELSQKVSEYKAAADAAAEEYTTAMWKLSNVVEPEAPEGGEDDYVVVKKVGQIRDFAAEGFEPKDHLTLGRDVAGIDMERGVKVGGSRFYFLRGQVARMQIAMLTMAVDQAQEHGFTLAITPTLVRPEVMRGTGFLNSHADEIYRLREPDEQYLVGTSEVALAGMHENEILDLSDGPLRYCGWSSCYRREAGAAGKDTSGIIRVHQFDKVEMFVYTKQEDSYKEHEHLLAMEQEMLGKVEVPYRIIDTAAGDLGSSAARKFDCEAWVPTQGRYRELTSTSNCTEYQARRLNIRERMEDGGTRAVSTLNGTLATTRWLVAILENHQQKDGSIVIPQAMRAYMGGKEVIEPTKWEA
>NZ_CP026729.1|WP_154303518.1|480062_481184_-|diacylglycerol-kinase
MGDMPMPVIIVIVVLAVAAVCAAFFFAVRAYKHRRFAEQLDKRDDDQVHYAFVINPSKPQAEQRKQHIQEFCEAKHLTQIEYIETQLDKDGRACALEALEHGADVVVAVGGDGTVRTVASALSGTGHALGIIPIGTGNLFARNMGIPVDDIDAALTVATSHGSRLVDVGRLTLLDDETADHGHAFLIIAGIGFDAVMIDDTNPELKKNISWLAYFVSGVKNLFAPKYKGDVTITSADGSTHTTHGLTFRTFMAGNCGQIPVFSLMPDAVYDDGILDYEIIDTSGGLIGWANLFGDVLHQTITGKAQQSPLSTNSTVDQIQGVSAEIKLEKPVLAQVDGDMLPETQHIRFSVERKSLCVRVPEAPDNNTANVNQ
>NZ_CP026729.1|WP_154303517.1|479156_480023_+|PRD-domain-containing-protein
MDVLRVFNNNVVLAKDGNSEVILTGRGIGFQAKPGQHVDDAKIVRRFVPAGGKDPDHMAQQVAGIPPEIIRLVTDAMNRAGLKEQADRQPALVLALSDHICGAIRRSQNKQTIEYPLEAEVRSLYASEYAKGKALVDAMNTYLGGALPDCEAVALALHLVNAGFSTGDLSATYTMTGVIQQILTVIESYYGINLDQNSVNVARFITHLRYLFVRIHQHEQLDDEPEPIVESIKTSYPKASDCANRLAIIIKMRLDASLSQAEIAYLTLHVARVTSHAAESHENNNINA
>NZ_CP026729.1|WP_154303516.1|477041_479129_+|PTS-transporter-subunit-EIIC
MAGSLASQIITAIGGPENVRSLTHCATRLRFELVDASKVDQNGLEHMQGVLGAVPQSGDRYQIVIGGGVATVYENIMHLPEMAGVGGASASDDGQKSNADVKAEARSKARGKVAWLDSFFEYLADSFRPILGVLLGASIIIALVNLLISLNVIPNDEASAGWVFVKAIWKGVFYFLPIMVAYNAAKKLKVDPWLGGAIMAILMTPQFTGLMDAKTTTCVENAALGTKSCTANIFGLPMALSDYSGNVFVPLLMAGALALVYHGLKRIIPESVQLVFVPFFCMIIVGALTAFIIGPIGVWVGNGLGVGLAWMNTHAPFIFAIIIPMLYPFLVPLGLHWPLNALMLMNIQTLGYDFIQGPMGVWNFACFGTTAGVLFLAVRDKDKDMRQTALGALAAGLLGGVSEPSLYGIHLRYKLIYKRMLVGCGLGGVVIAILGWLFPSVTAAGQTVHGVTTTAFAFTSLLTIPVFNQMWVYAVSIAVSFLTTFLLIITFDYRTPEQKAEVLARAAADQKASASSVEAKGAAPAAATAAATAVATKPEAPAAAATTVVNAPVAGHVISLDETGDPVFASRALGEGVGIQPADSEVVAPVTGVLQTVAETGHAFGIKTDDGVEVLVHVGIDTVKMNGEGFDVKVKANEHVNAGDTLVVVDFDKVKEAGYSTTTLMTVLNTVAFASVAPKTGVDVKAGESVIDIQH
>NZ_CP026729.1|WP_154303515.1|475042_476719_-|alpha-D-glucose-phosphate-specific-phosphoglucomutase
MVANNAGMPATPADLINVDEVIGKYYDVVPDPNVPEQRVSFGTSGHRGSSLKTSFNEAHIVAITQAIAEYRKKAGVTGPLYIGRDTHALSEPAWKTAIEVLVANGVTVRIDSRDDFTPTPVVSQAILTHNRAADGTQRFTGEGLADGIVVTPSHNPPTDGGFKYDPVTGGPAPADVTNAIADRANELLGDFKNIKRVPFEQAVKSDLVERFDFREHYVADLENVIDFDVIRSSGVRLGIDPLGGASVNYWPLMNEKFNLTIDVVRPQVDPTWSFMTIDHDGKIRMDPSSPYAMKGLVDSLNNGAWDKYDLVGGTDPDADRHGIVCPNWGVMNPNHYIAVCVEYLFGGNRPGWPEGAGIGKTLVSSSLIDRVAASIDAKLVEVPVGFKWFVDPLFKGEVAFGGEESSGMSFLRKDGRVWTTDKDGLIPDLLAAEITAKTGKNPAQLHQEQVERFGESWYKRIDTPTTLEQKQKFAKLSGDDVAATTLAGEDITAKLTEAPGNNAKIGGLKVTTENNWFAARPSGTENIYKVYAESFESPEALDKVLAEATEVVDKALAA
>NZ_CP026729.1|WP_157872354.1|474782_474953_-|GHKL-domain-containing-protein
MSSIGKRDGGPVSTKHGGTGLDTETVRRTAERHHGTATFDYGDDVFQASVMLCLDD
>NZ_CP026729.1|WP_033500853.1|473428_474709_-|ribonuclease-H
MTITVSTDGSALGNPNGPMGWGWADHELATGGKPGHHHEGDCDAGGATNGTNQIGELCAVLEALRAHPGSEPLVIETDSQYAINCSTTWVHGWKKNGWKNSQKKPVKNADLIRAIDAEISKRPGSVKFVWVKGHAGNAGNEKVDELARTYAGDCRSKVREGYLPLEGWQSLLASEYSQGIDVPDDAQMLLDGKITSDEYHIGRGQGESAGGSLTDDLIGASDPEPRPRSIADMLVEPEGYPTPDEATLPLPPNGMPAESDEMPEPTTVLATAVSDSTPSDTATSDSTQSDTTTPRKSYAEMLIKTDYFPREDAENTSDGTLQPTQSEQSATRSDESADSLQSPETQESLTDAPQSATQPQQSQRPRRKSPSGLSVSGTIRFTPPPNSSPTFDGRLRRIRGYIAVEGYVQGDGTLVLEDAPFAVKHN
>NZ_CP026729.1|WP_033500852.1|472555_473254_-|ribose-5-phosphate-isomerase-RpiA
MDKAQQDALKKAAGIEAAKLIQNGMIAGLGTGSTVRFLVDELGRRVQEEGLEFTGVTTSRRTQEQAEGYGIKIVDIDDVDHIDVTIDGADEVDKNFNGIKGGGAALLWEKIVATNSNKIVWIVDESKVVDTIGKFPLPVEVIPFGAGQVVKRFEARGYKPVLRLDAEGKPVRTDENNYVVDLHLERIEHPEALADDLINTVGVVEHGLFLHMVDQVIVGDPNGPRVLTNSNK
>NZ_CP026729.1|WP_004268639.1|472248_472338_+|AURKAIP1/COX24-domain-containing-protein
MGSVIKKRRKRMSKKKHRKLLRKTRHQRK
>NZ_CP026729.1|WP_154303514.1|471419_472046_+|hypothetical-protein
MSNTQTSSSHGKLIAAVVAAALVVVLALVSAFIWPGWALNKGGEARSQGTTSQGASQGASEPTTPSIDAVALPDDASELLKAMPDSVLNFARTKAAAGTSWSGASPVEEYTLTYSTGTDGQEVTLEVAQWSQGEDAQSQYDNLTGAMTGKELGSGNVKVSGEATGAYSAKTDPNDETKAIAVWRNDTVVFQATGAKDSVRRFYQQFPL
>NZ_CP026729.1|WP_154303520.1|483202_484255_+|ADP-ribosylglycohydrolase
MRKNGMQMKDQAMGAMAGLALGDALGMPTQSMSAEQIRQYYDGPITKLMNAVPQQPIAPNMKAGAVTDDTEQAFVLAQRLIDDNGCIDNTRYAHDLLQWEAAMKAKGSLDLLGPSTKAALQKLTEGVSLEETGRFGTTNGGAMRATPVGIAFRPGQALADAAWQSCVVTHNTVQGIEATTLVAAAVSFAIEGERDFLHLAVEFVQKLPQRGNWSAKASVLARVQYFMNWAETDGCRLNDDEFAAVLQRDCGTSVESNESVAAAFAIAARFFDDPTHALCFAASIGGDTDTIAAIAGAMLGAWHGMQGFDKTMLDQVLSQLAEDNHLDLVGTVTSLSALRDDSALNDANIV
>NZ_CP026729.1|WP_154303521.1|484308_485310_+|hypothetical-protein
MTGKVISLGQVIVDLTMNVDAVPRAGEDVFAGNVQTQVGASFNTLYAVRRMGVKASHAGVIGTGPWALQILQTLENQGIQHIGKRDAVRDSGFCVALTDANAERTFISTRGAEAYGSVDAFDSVNPEKQDVVHVSGYTLVHHTADALLAFAKRTTEHREFTAVFDPSPMIATVDDDVFRVMLAYRPIWSCNEREATLIAQRLVALDNGNSCDCKVSQDILQAIENANVDEETVAWLCNRLQSPVIVRVGADGAWLAIPGDEALRIPGFPMKAVDTNGAGDCHAGVLCALLCEGVPLKDAVRCANAASALAVTRSGPATCPDRKEVERLLGRVF
>NZ_CP026729.1|WP_033500861.1|485425_486877_+|allantoin-permease
MSNEKGTLSIEEQGIDTISEEERKGTPASLFWPWFAANVSMFAMSYGAWALGFGISFWQATAMTIIGVVVSFLLVGIISIAGKRGNAPTMVLTRATFGVEGAKVPAALSWIATLGWEISLTTTAVLALSSTIEKLGWGSGAAPKIISTIVVVSLVVVAGIFGYDLIMRCQQVITIVTGVITVGFFILGWGHIDFSAINSVPAGSLPAMLGCCFFVMTGFGLGWVNIAADYSRYLPRKSSNGGIVFWTTFGASIANVFLIFYGLLLAVSNADMAENVGNDPIGAIASILPTWYLIPYTIVAVLGLMSGSIMDNYSNGLALLSFGVKLPRTVAAAFTAALTVLGVVYVTFFSDTFIGPFQGFLTTLGVPMAVWAGMFVADVIIRKKDYSTADLYDSKGRYGAWNGKSFAILIVGTVLGWGLVVNTAASWLNWQGYLLFLIGGKDGSWAAANLGVIVALVVGLAGSLIFQRGDIAKQEADLPVSEV
>NZ_CP026729.1|WP_033500862.1|486924_487485_+|cysteine-hydrolase
MIAEDEWLVVIDRQRVFAESEWSAWACPDGSYHTTDEAFARLARAFGDRVVYTRYVAPEPPQNAWVDYFKNWPQFLVAPDDPMYDLTADTAELAQGHAVVSCDTFGKWGSVLSEAIKGAKKITVCGVATDCCVLTTVLAAADNGVAVRVAADACAGSSPENHQMALNTMALFTPLVTVTNTDAILK
>NZ_CP026729.1|WP_003835555.1|487703_488390_-|response-regulator-transcription-factor
MNEQEQQIRIAIVDDHEMFRAGVIATLQPHFDIVGQASDVEGSVAMIAQTKPNVVLLDVHVPGGEGGGGAEILMKSRAYSPNTVFLALSVSDSPQDVGSVIRAGAQGYVTKTISGDDLISSIKQVYEGYAVFSPKLAGFVLSAFQNGSPAGIGGSASGPIHDDELDRLSNREQEVMRLIARGYTYKEVAAELFISIKTVETHVSSVLRKLQLSNRTELTRWAADRRIV
>NZ_CP026729.1|WP_154303522.1|488386_490003_-|PspC-domain-containing-protein
MKSLGKPWYTQSQYDQASAVYMRYCCDQALHEGRPLPTRPAKLPLMRPPYGRMGAGVCKAISMHLGIAVLWVRLFFLATTCLFGAGLIAYIFLWMALPVGDPVQQAYIIAGKRSPWQAPLSRGNMPYGTYPVSPEYQSFTATQDGQHTQPPSFEDTTERNDGTYDNTQSSSENLEQTLKKAPKPALLALAGLILLSICFVMFAGGVERALIVPLLLGLVGIGVSWLRFNAEEGQLWTMLGGIALIFAAYALYVSSCIHFDAFSMIRILCAGLALLIGVLLAIVPWIMALIRDLGTERASKEREEERADMTAHLHDGVLQTLALIQLHADDQQTVFSLARSQERELREWLYQERTTSDRSVNAGLKEIAAHVEDTHGKPIEVVTVGDARPSAQTDALLDATQQALINAVAHGGEPISVYCEASSKLVEVFVRDHGNGFDVNAIPANRLGIRESIIGRIKRRGGTVEIVSRPQWGTEVRMHMPIADMPASAAADTNAQQSHEPQSNSQQTDFPDHHNRQSNNQRTNQFSNQPTNHFEEQQ
>NZ_CP026729.1|WP_154303523.1|490116_492039_+|PspC-domain-containing-protein
MSNANNDPLGDRGNAGPQPAAGQPYYQQPAYGSPQPSRGGRFFAWIRSSQVKRGHDRWIGGVCDGIARRLGWNTTLVRALMVVATLFFGAGAAFYGLAWFVLPDERDNQILAEDLINGKWDWNCIGALLCCLVAICLPGAGWFAFALAALVLWLLLNRQIYAPNVPPNQWQQPPYGQAPYGQPQYGQPQYGGPPYGQPVPPASPSSAQSNPYTQPMQASGAYNGADSTASSPESQSPQPQRPQPQQPQYHAYQQQVNGPAAFATANVPPTFTAPAAPVAQAPRSPKYGRRKPAGPLLVLMMFGLTMIACALCVWCIMTYGVQGGQRGTEYTLQACAAFVGGICLVTGIVIVALGFAGRRTGGLHPLTWISIFMSLVMVMALASYSLFSYRINTGISSSYKRVNVSGITTMGSTASEMSRYEQGIVAQGNDYATDVLHIDLSDYAKNNGPHKVDLQDGTQGTTSCPTGTLNVVASSAQVVVTLPNGCWWAFGSDGDFYNITDFVGSSDGLTLDSGNIYVSLMGNDSTKSVVKKRALGTYDWSCGSYGDESGIEDFDDETATEDGTDTGADSTRTDSPFKDGDVDKAYREIYDNHQYWPCFTGDDKAPVRPAGLRINTMATVGGSVAVQYASDNTLGKAGKE
>NZ_CP026729.1|WP_154303524.1|492041_492617_+|hypothetical-protein
MSDDKTQEMPVMTDAGDMPTETLHTVDAQSTYDHSQHSGRATQDDKPRVESVPAQSVPTYTASAAGANVGHKNRQIGDDIIRPFGRSGSTIALGVFTCFMGVVTLLCGMHVPMNLWWWASDPKQFFVFLLGGIGVLLIAVAVIWVIVSAVHSNRSKNGNDVDSDDPFDAPYNSNTTAFSTDSDKSPLSERS
>NZ_CP026729.1|WP_154303525.1|492831_493479_-|DUF4125-family-protein
MNSNVISDVIDGHDTANLVESIIKLEWNQFQQTNNEGGRASCQGNWPMFHQMRASQFMTWPEELLRSYRSDLQEADRVGRNLVTEKYGRMMQSTYPQEYCANIAPYIPQISAGRNALQEGIITVQVAWARDFRERFPHLGEAMRVLTTVEDTPETTSFETYLRGELGTYSDRTVALYRDFVERLRHEQRNLTEETIRNTVRLAGFEDLAQAEAAQ
>NZ_CP026729.1|WP_154303526.1|493549_495718_-|DUF4037-domain-containing-protein
MPSAVREMMEVTDEGIAMADSDVNLNMNNCDDGCATFAVQRFLRGLDAIFDAHKAPEQAEPYLQKARTEAEHSHDDAGLLTVLNETMGFYRSQGRHTDNLPIIRESLSIADHLHLQEIDPQAWATTLINAATGMRAAGQYEEAEQLYRQALDAATSAFSPTDRRLAALHNNMSMLYSETGRLNQAKRELEQALDLLEQSSPDASADIDVASTRTNLALLLLQMDRHWASDAIQHAQKALTIYRTGHLEHSAHYASALAGYAQACYMAGCLQDAVSGYEHALSVIEECYGRNTDYYHTTAANLEAAKQALHKHMPSAHKTRESQEYQESQESLKSQHSPKSSESQQSSEPHYMTESGASSIPAISHHISGLALSRAFWNDLGKPLLAGAYSAYQGRIAAGLVGYGSECFGFDDEFSRDHDFAPRFCLWLTDEDYDAIGEQLQADYDALSRDFTVDEQGKPHFAGHGSADSNALAASQSPLTPRAQGEFRRDGVFRIGDFFERITLFREAPAQNDYASWLSLDDATLATATNGQVFADPLGVFSKTRQGFKFMPEDIRLSLISRRLGMMAQAGQYNLLRMLQRGDGAAAMLSIHEFVNATASLVFLINEPVSVGYLPYYKWQFAAMRKLSRRMATRLAGVCEQLEDILRLSSAACFGGAGFGEGGKGAKPAAEHIIATVERICSDVVDELLREGLTESHETFVEWQRPYVEDHIKSDASCLHSL

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Crispr_ID: NZ_CP026729_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_4

2039714-2039830

Orphan

Consensus_repeat	Method
AGGTGTAATAGGAGCCGAGGGAGTCAATCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP026729_4

>merge|NZ_CP026729|4|2039714-2039830|CRISPRCasFinder
AGGTGTAATAGGAGCCGAGGGAGTCAATCCACCGCTTGGAGTCTGCGAACCAGCACCAGGATTACTACCGGAACTAGGAGTATTGCCAGGTGTAATAGGAGCCGAGGGAGTCAATCC

>NZ_CP026729|4|4|2039714-2039830|CRISPRCasFinder
AGGTGTAATAGGAGCCGAGGGAGTCAATCC	ACCGCTTGGAGTCTGCGAACCAGCACCAGGATTACTACCGGAACTAGGAGTATTGCC
AGGTGTAATAGGAGCCGAGGGAGTCAATCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154304182.1\|2050339_2051614_-\|divalent-metal-cation-transporter	unknown	unknown	gnl\|CDD\|234815
NZ_CP026729.1\|WP_051920277.1\|2023898_2024450_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225420
NZ_CP026729.1\|WP_154304426.1\|2049042_2050362_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP026729.1\|WP_154304173.1\|2028157_2029618_-\|IS21-family-transposase	unknown	unknown	gnl\|CDD\|226950
NZ_CP026729.1\|WP_034255053.1\|2033362_2035105_+\|ATP-dependent-helicase	unknown	unknown	gnl\|CDD\|223288
NZ_CP026729.1\|WP_033501501.1\|2051724_2052579_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381357
NZ_CP026729.1\|WP_154304176.1\|2037884_2039156_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304181.1\|2047310_2048852_-\|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|129794
NZ_CP026729.1\|WP_154304172.1\|2026199_2026805_-\|low-molecular-weight-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|319971
NZ_CP026729.1\|WP_033501502.1\|2052692_2053436_+\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|377857
NZ_CP026729.1\|WP_033501997.1\|2022033_2023227_-\|glycosyltransferase-family-1-protein	unknown	unknown	gnl\|CDD\|340858
NZ_CP026729.1\|WP_154304425.1\|2046965_2047292_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_048349540.1\|2044809_2045430_-\|protein-tyrosine-phosphatase	unknown	unknown	gnl\|CDD\|319971
NZ_CP026729.1\|WP_154304180.1\|2045634_2046651_-\|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl\|CDD\|197318
NZ_CP026729.1\|WP_154304178.1\|2041316_2042792_-\|polysaccharide-biosynthesis-tyrosine-autokinase	unknown	unknown	gnl\|CDD\|349772
NZ_CP026729.1\|WP_154304171.1\|2024710_2026084_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_162008510.1\|2030006_2030420_+\|transposase	unknown	unknown	gnl\|CDD\|366234
NZ_CP026729.1\|WP_154304175.1\|2031359_2033348_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226121
NZ_CP026729.1\|WP_033501998.1\|2020826_2022029_-\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP026729.1\|WP_154304179.1\|2042936_2044742_+\|DUF4012-domain-containing-protein	unknown	unknown	gnl\|CDD\|379067

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154304182.1\|2050339_2051614_-\|divalent-metal-cation-transporter	gnl\|CDD\|234815	PRK00701, PRK00701, divalent metal cation transporter MntH.	1.54352e-136
NZ_CP026729.1\|WP_051920277.1\|2023898_2024450_+\|hypothetical-protein	gnl\|CDD\|225420	COG2865, COG2865, Predicted transcriptional regulator containing an HTH domain and an uncharacterized domain shared with the mammalian protein Schlafen [Transcription].	7.31481e-25
NZ_CP026729.1\|WP_154304426.1\|2049042_2050362_+\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	1.09254e-33
NZ_CP026729.1\|WP_154304173.1\|2028157_2029618_-\|IS21-family-transposase	gnl\|CDD\|226950	COG4584, COG4584, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.0167e-17
NZ_CP026729.1\|WP_034255053.1\|2033362_2035105_+\|ATP-dependent-helicase	gnl\|CDD\|223288	COG0210, UvrD, Superfamily I DNA and RNA helicases [DNA replication, recombination, and repair].	6.36168e-21
NZ_CP026729.1\|WP_033501501.1\|2051724_2052579_+\|aldo/keto-reductase	gnl\|CDD\|381357	cd19131, AKR_AKR5C2, Escherichia coli 2,5-diketo-D-gluconic acid reductase A (DkgA/YqhE) and similar proteins. Escherichia coli DkgA/YqhE is a founding member of aldo-keto reductase family 5 member C2 (AKR5C2). DkgA/YqhE (EC 1.1.1.274), also called 2,5-DKG reductase A, or 2,5-DKGR A, or 25DKGR-A, or AKR5C, catalyzes the reduction of 2,5-diketo-D-gluconic acid (25DKG) to 2-keto-L-gulonic acid (2KLG). It is also capable of stereoselective -keto ester reductions on ethyl acetoacetate and other 2-substituted derivatives.	1.17893e-122
NZ_CP026729.1\|WP_154304180.1\|2045634_2046651_-\|endonuclease/exonuclease/phosphatase-family-protein	gnl\|CDD\|197318	cd09084, EEP-2, Exonuclease-Endonuclease-Phosphatase (EEP) domain superfamily; uncharacterized family 2. This family of uncharacterized proteins belongs to a superfamily that includes the catalytic domain (exonuclease/endonuclease/phosphatase, EEP, domain) of a diverse set of proteins including the ExoIII family of apurinic/apyrimidinic (AP) endonucleases, inositol polyphosphate 5-phosphatases (INPP5), neutral sphingomyelinases (nSMases), deadenylases (such as the vertebrate circadian-clock regulated nocturnin), bacterial cytolethal distending toxin B (CdtB), deoxyribonuclease 1 (DNase1), the endonuclease domain of the non-LTR retrotransposon LINE-1, and related domains. These diverse enzymes share a common catalytic mechanism of cleaving phosphodiester bonds; their substrates range from nucleic acids to phospholipids and perhaps, proteins.	1.033e-18
NZ_CP026729.1\|WP_033501502.1\|2052692_2053436_+\|HNH-endonuclease	gnl\|CDD\|377857	pfam07510, DUF1524, Protein of unknown function (DUF1524). This family of uncharacterized proteins contain a conserved HXXP motif. A similar motif is seen in protein families in the His-Me finger endonuclease superfamily which suggests this family of proteins may also act as endonucleases.	1.30073e-23
NZ_CP026729.1\|WP_033501997.1\|2022033_2023227_-\|glycosyltransferase-family-1-protein	gnl\|CDD\|340858	cd04955, GT4-like, glycosyltransferase family 4 proteins. This family is most closely related to the GT4 family of glycosyltransferases. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found in certain bacteria and Archaea.	0
NZ_CP026729.1\|WP_154304181.1\|2047310_2048852_-\|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.24478e-72
NZ_CP026729.1\|WP_048349540.1\|2044809_2045430_-\|protein-tyrosine-phosphatase	gnl\|CDD\|319971	cd16343, LMWPTP, Low molecular weight protein tyrosine phosphatase. Low molecular weight protein tyrosine phosphatases (LMW-PTP) are a family of small soluble single-domain enzymes that are characterized by a highly conserved active site motif (V/I)CXGNXCRS and share no sequence similarity with other types of protein tyrosine phosphatases (PTPs). LMW-PTPs play important roles in many biological processes and are widely distributed in prokaryotes and eukaryotes.	3.03161e-32
NZ_CP026729.1\|WP_154304178.1\|2041316_2042792_-\|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.	3.05149e-61
NZ_CP026729.1\|WP_154304172.1\|2026199_2026805_-\|low-molecular-weight-phosphatase-family-protein	gnl\|CDD\|319971	cd16343, LMWPTP, Low molecular weight protein tyrosine phosphatase. Low molecular weight protein tyrosine phosphatases (LMW-PTP) are a family of small soluble single-domain enzymes that are characterized by a highly conserved active site motif (V/I)CXGNXCRS and share no sequence similarity with other types of protein tyrosine phosphatases (PTPs). LMW-PTPs play important roles in many biological processes and are widely distributed in prokaryotes and eukaryotes.	9.34444e-33
NZ_CP026729.1\|WP_162008510.1\|2030006_2030420_+\|transposase	gnl\|CDD\|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	1.16699e-09
NZ_CP026729.1\|WP_154304175.1\|2031359_2033348_+\|AAA-family-ATPase	gnl\|CDD\|226121	COG3593, COG3593, Predicted ATP-dependent endonuclease of the OLD family [DNA replication, recombination, and repair].	1.34368e-35
NZ_CP026729.1\|WP_033501998.1\|2020826_2022029_-\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	1.7647e-41
NZ_CP026729.1\|WP_154304179.1\|2042936_2044742_+\|DUF4012-domain-containing-protein	gnl\|CDD\|379067	pfam13196, DUF4012, Protein of unknown function (DUF4012). This is a family of uncharacterized proteins found in archaea and bacteria.	1.73293e-40

>NZ_CP026729.1|WP_154304176.1|2037884_2039156_-|hypothetical-protein
MYKHEKQAVERLQSNHIHMLSTLSTAIIAFFLIISLSGTMLFPMMAFADEPQPVAQVGDTTYMSVQDAIGHTSMKNNTVTLLTDTTESVTVTPSKVVRGITLELNGHVLNASNTTAITVPANMQLTITGSGTVVGGDNPAIDCRGALRIQGGNFTSNTTLMRFAETSGASAEASISAGTFTAPTLIGMLDDAEHLGYASIRGGEYHGAIPAGLDTLVLMGGSFSTTENLTPYLADMVGLIPNGDDGMFDISELAISSDYPTVALEQGSTLQNLTNDSLLDLTRTKLNGISDYRLVADAEQLQALNKQIELALQAVAKRKAFDAVNQTVTITATRNTEIADGGAGPQFRTSGHDEISTQVTVNIKSIAKPEEPDKPDEPGKPAEPKQPDMPRTGSAIQALAVASLLLLVAAAVCAFVTSRLRSS
>NZ_CP026729.1|WP_034255053.1|2033362_2035105_+|ATP-dependent-helicase
MSKECIGVNYGLAKAEADKVDARIIEALKSGHSFRVEAGAGSGKTYSLNRVIEWIQANKWSAYNRKKQNVICITYTNAAVDVIAERLAKDSFILPSTVHSFAWNAIKQYQGVLIEAVTTNPDYLPDEGDFNQVTEVAYTLGHRYKENGVQYLYHDDVLKLFCQLLDNAKFRRVFADKYPLILIDEYQDSYKPIIDRFINFFIAKSTGPQFGFFGDAWQTIYQSNKACGEIKHEKIEVIKKGSNFRSAPRIVQLLNNIRPELPQKSAIDGFDGEVLVITCDDYSGARRTERNFKNELPAAEFKARLNTIVTKIEQNTPADEDLKVLMITHKVLASQQGYEQLLDILNDALRNKEDPFLIFFADTIESIYHALDTSNTQLLFDTLGIKRYPITKKSEKTKWKTLYEQLTEVRTQKAIDVLKTIIDSQLIPIPPKVDGWYRLYMDAPETMYASKATIQQFLQLDYAQFIAVRDFLYPDAQFSTEHGVKGEEYDNVVFVISRGWNQYQFETYAPMITGHASIPKGKEASYERNRNLFYVCCSRPKKRLFFFVTVPIDSSFRTFLVKLTGEESILTYRQFMEASN
>NZ_CP026729.1|WP_154304175.1|2031359_2033348_+|AAA-family-ATPase
MQLSKIKIKNYRLLIDAELEVDSRTTLIVGRNNTAKTSCFSCIGKVLNGEAVSFDDYPLLRRKDFYTKIALFMEKKLTYEDLCKHIEIISIDFLVDYSLDDLDDNLGALSPFIIDVDVDTTTALIRAEYRLKTDEKTLWSLLESSYYKDGAYSPSEEAHKVLADNFGKLFGLTVYAINPNNPEDKQVKSQKELYDLFPFHAIPAERVLGEDDAHNSSLGLLISGFFDTSEAELDPDVATEIKRLRSIVEKANKDVQKQSDEILSSVVNNSIGFGYPNIEELKLGVTTQLSIDDQIKNQTKLSYISGTANESLPSSHNGLGYKNLIKMEFLLAAFAKDIEKRGVACVPLLFIEEPESHMHPQMQTAFAAYLEKFLGKLSDVKIQTFLTSHSAHIANTMKFSKVRYTQKSNTGVIYKNLNTFAQDHPNNVDFIRKYLTLTKCDLFFADKAIFVEGASERLLLPDMIEKCEKSGEFSYCKYPLSAQYYALIEIGGAYAHKFIPFIDFLGVPCLILTDLDSVANSKGKNGKAVKKSVIVSQGETTSNETIKWWIRRNKGISENNTSKINLSEIKAITADDKTRGKCHIEFQTTENGLCGHSLEEAIRNVNRKHYNLSDKISEDELEFKGKSKTDFALDLIYKYSDYCVPDYIKSGLKWLNDQRVLE
>NZ_CP026729.1|WP_162008510.1|2030006_2030420_+|transposase
MSAGRSGGQGHCRPFRRADPGRGPGAAFATLDFPLADVQVFRTDRGGEFDNTRIDEPFDVFDVKGSLSRKGNPYGNAVVESMNRLLRKELVYRNHHTTIEQPGRDPDGCVWCSDDQRLHSTLGYRSPKEFTEQGLVL
>NZ_CP026729.1|WP_154304173.1|2028157_2029618_-|IS21-family-transposase
MTTPVCVRQRIRQLDRQGMSHKEISRRLGVSRTTVVRYANHGDYSPRPSNAVLPGRSLVDDGYAAIVDGWPAADLRMPVKQRHTATRVYERLGAERGFTGSYSSVRRWVKRWRREHRMESDGFAELEWVPGSAQVDFGQARAVIAGVERVVHFLAVSFPYSNMRWVVALPGETSECVCQGLLWIFGRMGMAPGVVVFDNATGVGHRRPDGTAARTRLFSLFCAHYGFESRFRDPYSDHGKGSVENAVGFVRRNLMVPMPSAESFQTLTRVWLDACERISGSDHYRHGVPVRELFEAEKDHMLPLPGVRFDPCDWRSVKTDKTGAATIDANRYPAGPRWRSMRLQAGVRVFEIELRDPDGGHIVTLERVWGKSARTQVDPASLLAIIARKPRIWGESPIRNDFPETVRALLDRMDARTRSNLLDDIRAVAADCGFAATVKAVETVINAGRTVDRTAIGTCAKRILEGAGTEGGQDLKRYDRYMKEAE
>NZ_CP026729.1|WP_154304172.1|2026199_2026805_-|low-molecular-weight-phosphatase-family-protein
MHIMFVCTGNICRSPMGELLLTRYLSGTTVQVSSAGTHGLPMHQIDPNSALLMESVGIEPSGFRSRRLTQPMAKSADLILCFEKDQRKDIVTLAPTAVKYTFLLGDFANMCEYCARNGLVKGLTIQERLQSVIDSASIIRPMLPEPEDIEDPHGKEYAQFRTAAEQTNKALRTILTSMRKHYRVEEAPVRPQITRQYAYTV
>NZ_CP026729.1|WP_154304171.1|2024710_2026084_-|hypothetical-protein
MTDSNIAGIAEADFGKAGVSFDNDRPILVDSSDFLFYAALAMLPIDGTVAGPYMPFWTPLSPWLFMAYAVANWRLLPQVWHRFRAFFLFPVLLIALSAVDWYLVAFHRLPALVSLAGVAGALACLCALDMALRIKRLSWRRMLDLLILVYWFAFAVGVVQRLSIMFDWTSVKNFFIHLMSRQYISSTSHWGGGRPQFLFAEPSYIGMHLFGVLLPLIWLVRGRDHKRANQLRVLIMVFAAGSVIMGAGVRIILDSIIALVFVIIEMNSWHTWRGRLVAFGELVVTVGLGACSVAVNHRLSSIAELGFDGDGSFYARLWQSLGPGAGALKHPKQLLLGYGAGNLSDATHQGADAAVRSLERLGLNASAPKGWYAQVTPANMFTMSAYTSFFVEFGLIASVILVVLVLWWISHNHAWNKTTVCWLLLTIYLYVQFEGYAFYALPLLLWAVAAVPRLKSK
>NZ_CP026729.1|WP_051920277.1|2023898_2024450_+|hypothetical-protein
MDWYRQEFDIPQTASTQQTLHLLASEQLIIAQDAGNYAITNLDALLFARDFNDFPTVARKALRVIRYDGPSPISPSRSKTFFSGYAKLDQALEYVEALLPEQEVIQGVRRVTLRMFPHMALRELMANMLIHQDFSITGTGPMICIFDGRIEFTNPGSSLVDVARLLNDLPHSHNEKWQLFADD
>NZ_CP026729.1|WP_033501997.1|2022033_2023227_-|glycosyltransferase-family-1-protein
MSGVSAVQHVFVVGSKGIPGSYGGYETFVDRLTEYHEGEPGLRYHVACKSLSESGEFSYHNARCFRVRVPQIGPAQAIWYDVAALADCVAYIRRNRIPHPIVYVLACRIGPFTAHFARAVHRLGGKLYVNPDGHEWMRAKWSAPVRRYWKVSERMMTKHADLMVCDSVNMEKYIREEYARYRPQTTFIAYGAEDRRSRLADDDPKLLDWFRSKGLEPKSYYLVVGRFVPENNYETMIREFMVSNSKRDFALVTNVSDKFLEELKEKTHFDRDPRIKFVGTVYDKELLMKIREEAYAYFHGHEVGGTNPSLLEALASTDLNLLLGVGFNREVAQDAALYWSKEPGDLAALIDHADAMSPDEIHALGARAKQRIADAYSWQHIADQYKNLFLGREQKEG
>NZ_CP026729.1|WP_033501998.1|2020826_2022029_-|glycosyltransferase-family-4-protein
MKILAIHNFHRSGSASGDDQVFKSETSMLEEHGHEVIRYTVSNDEFDKADAAGKLAATFGMLWSFKNYRAVVSLIREHHPDLVHVHTFFPLLSPSILYAAKRMGVPVVATLHDTRFVCPVATSLRDGKICNECGDGHYLRMTRHACFKGSRLQSLLVAGIFKYHRARRSFYKQIDRYICLNDNQIDLLKGIGFDSSKIVKKYNFVPDAQANMAAERVSGLPERYAVFYGRIGAEKGIRVLQRIWNEIDDIPLVVMGGGPLEDDFKAWADKKPNVYFLGYTPHEQCMAIAKAGEFVVFPSIWYEGCSMVEIESESLGLPLIATDLGFSAEAVNDGVNGVKVPLGDMHGWVTAIRGLWKEPELCKKMGMNSRRDYEDKYTPENNYQQLLNVYRGIVSSTARR
>NZ_CP026729.1|WP_154304178.1|2041316_2042792_-|polysaccharide-biosynthesis-tyrosine-autokinase
MRGSVTSAENTNVQQVAVEEDSEDGITLMDLMRIIRKHLVTAAIIFVMVFAGVAAYTFLVPPKYTATAQAMATYNASQGDDAGISQQYTGGTYIAGQITSYTTLATTETVLEPVIKDLGLDTSVKSLAEQLTVTNPTDTAFVNISAEDGDAQQASDIANAVAVSMQNVIQNDLYSAADKSPVKISIVQRARVPESPSSPNKPLYLAVGVVAGLVLGVFAALLKDMLNTKVEETSDVRSLVGASSLGSVPQDNSLGEKRPVLVSQPNGPIAEEFRRIHTNIEFLQTDKVAGKGQLLVITSAQPSEGKTTTSINVAAALAEDGARVLLVDADLRHPSVAHHLGLEGSAGLAHVLSGQMSPKDVVQNYWKPTLHILPAGKRPANAGVLLGSDTMRIMVEQALTQYDYVIIDTAPLSVSNDGIVFGRWAKGLVLVTGRGVCEKKELKEISESLHVAKVPVLGFIFNYADLKKTHSNSNYYYYYYEDAPRKKSHKK
>NZ_CP026729.1|WP_154304179.1|2042936_2044742_+|DUF4012-domain-containing-protein
MSQHASAHAARSHKLRNTLLVITALLILLVIAGGVIGLNFYKQAKEVKAHEEQAVSSLSAITNVNTLKDAQASDAAIQQAQTHTAAAKDIANGTLWNMLSKMPVVGGDVTNVQDMTQVVDDLVQQTLPSLTDVVQQLANAQISGENGQLNLQPIVDAQDDFSSVSKQVKSLNSKLSNLPEPRIGMVKKAYSQSRSQFTKVTDMVEQVNNALQMLPSFLGQNGVRTYLLVAQTTSEQRSGGGLVGSMGTLQTDHGQIQVGEFHHNGDFINGSNGNASEHAVFKGPLGFSFDIRDTFAVPDIARNAEMMNEAWQRSQYACDVDGIVSIDPVFIQKMVEINGNVTLEDGTVLTGKNTAEYMLNTIYKEVPVSLQDTYFEYIASTIMNNAFSNMDITKMMKVAQSIGELTKNRHFYAYTFHDDEAKYFQGAGLAKGTPDSETDPEVGIYLNEQNPSKLGWYINRKAQITKTGQNADGSKTYHVTYTLTNTLTSSEMATCTGYILGGEQAGVTGKPVAAPGTSAQRMLFYAPKGGSISEITSSGDVRDQSNAVMDGQKLVTNVAYIAPGESVTFDFDVTTSPKAESDLTIDQTPSGKMTNEVNYQY
>NZ_CP026729.1|WP_048349540.1|2044809_2045430_-|protein-tyrosine-phosphatase
MHIMFVCTGNICRSPMGELLLTRYLAGTTVQVSSAGTRGLPRCQMDPSSARLMTSVNIEPSGFRSRRLTRSMAESADLILCFEKEQRKDIVALAPGAVRYTFLLNDFANMCQYCAQNGMVSGLTIQERLASVIKVSSMIRPMLPTPKDIDDPHGKSFDKFRIAANQTNNALRTMLKSMKKHYSMGIAPVRSQICSGQPITTYNMWA
>NZ_CP026729.1|WP_154304180.1|2045634_2046651_-|endonuclease/exonuclease/phosphatase-family-protein
MTRLGDAQRNETRRETRSTLLTVLLWLVTAVIVVAMLLRMLPNNLDGKRYVPLVVALMPWLGLLSAVIAVFALTIRRIGKRRALAALSAVCVVIQVAWHWGYIVPAASPVSQPTATVRVMTFNTKQGVADAQQIVEAIREEHIEVLAMQEVSSDLLNRLNDEGIADYLPYSITPQLTWHDNGGVNVLYSAHPLQETTENLIPIESSSIPAATVVLNGRNVRFGSVHPFSPRPRNQGLWNKSLDSIAQLQHYDNNESYVLMGDFNSTWDHASFRYLLGDRFTDAGQSAGEGLHMTFPAVFPIAEIDHIIYDKGVRATDLATKRIQGSDHLALLATLTIA
>NZ_CP026729.1|WP_154304425.1|2046965_2047292_+|hypothetical-protein
MMSEEAMREEVAQAVEVAANKAAKEEISKLAEFESAIDETLASGYLDDTLTVTDADGVAQVLPVLDSEPISHLVEGLEAVGGSANVFVRTSAGVVALSVVEYKPNEEE
>NZ_CP026729.1|WP_154304181.1|2047310_2048852_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MSAKRSMSRALTREESYQNGHLTRTAFISIAILTFITFVGNFTQLQLSAALPTIVSDFGISVTTGQWLTSIFQLVMGVMVPLTAYLTRRFSTREIVLVSMVVFTIGSLFAWIGPTFLMVLIGRLLEAVGTGVMWPVLQITVFSIYPLSRRGFAMGTVGMAMSVAPAIGPTLGGVQTDLNGWRSIFLTLTIIGVISLLLAYFGLHNFGENDKTAKADFFSVGLSVFGFGGLMFGFTNIESYSFVNPMVWLPMVIGVTGIIWFVFRQIHGARRQIENPEAQPPLLNLSVLKNRSFTVGTITAALAFFAFSSIMVIMPLYIQDCRGYSAAISGLVMLPGALGQCISQFFGGKVLDRFGARPVALIGTITLCFGTVMMSLISMTSWIWWVSIWQFVRQIGMGFVLMPITTWSLNCLEPEEVSAGSAVTNTVRQIAGAIGAPVLVILMETFTSLRWTTLGGTKAVYAAANVFGIQWALRVSAAICFVMVLMVFFGVRGQGAGSTHETVQRALNRRRAA
>NZ_CP026729.1|WP_154304426.1|2049042_2050362_+|diguanylate-cyclase
MTVRAMFHICMESWGIFICLICAGGIFIATPQKTRRTRIKILMQIACMLLLGADALGWYFLVDAGETAYYMVRISNFSVFCINYIFMSFFATYVWLTASKHHHRRPAALYAVYALSVIGILLLIITQFTGLFYYFDDHNLYHRGNFYLLSQAVAVLGIILCLFMLISYRKNLDRIVFLSMMSFFVLPTLATIYQALAYGFSLQCLATVISTQIMFVMDTVEVNMRFHSQQAAYEKARYEAEHDGMTGLLNKEAGWKHMRKYFDRMDSHDEAMLMFVDIDDFKTINDTYGHTVGDFWIREVASQLRHIYRQDDIICRYGGDEFMALIRNTASEQVLETTLGMFFQQLARASEQRGQDVHCSVGVCRIAATRISGNRVISRNTDGGNGEDTRGGVDFDQCVKQADLALYETKRFNKGTFTVYDYDRPQQHPQSASRSGRKV
>NZ_CP026729.1|WP_154304182.1|2050339_2051614_-|divalent-metal-cation-transporter
MEGNMDSKNAITTPQPQSHQHYGHALAGILGPAFVAAVAYVDPGNVAANVTSGATYGYLLVWVLVLANCMSVLIQYQSAKLGIVTGRSLPEILSERLGNAGRFMFFMQAEVIAIATDLAEVIGGAIALKLLFGLPLFVGGCIIGAISTVLLIFQKGPTHRLFEKMIIALLLVITFGFIAGLFIDPPNPTQVATGLIPRFKGSATVLMAASMLGATVMPHAIYLHSTLVNDHYSAGQKKPDIKTLLYGSKVDVIWALLLAGTVNLALLILAANSLYGVTGTDSIEGAQHAIAAALGPVVGTIFSVGLLASSLSSTSVGTYAGAEIMHGLLRIKAPMWACRVVTLVPALVVLWFAKNPTEALIMGQVVLSIGIPFAIIPLMKYTHDRSLMSDHVDGPVKFAINMIVVSLIVALNVILVFLTLSGRS
>NZ_CP026729.1|WP_033501501.1|2051724_2052579_+|aldo/keto-reductase
MATFHTPMVTLSDGNLIPQIGLGVLRIDDEGVTPVVESALEAGYRHIDGAAGYNNEAGVGRALRNAGFTQGEHRKNLWVTTKLRDSEQGYDSARKAFDRQLGLLQLDYVDMYMLHWPTPFNWRSGETWKAFTEFRAENRVRTLGVCNFMPEHLDRLYEETGEYPAVNQIELHPTWQQREVVEYCKAHDIAVEAYSPMARGADLNAGNGTIERIAAAHGITPAQVILRWHIENGTIIIPKSVHADRQKQNLDLFGFVLAPEEHAAIDALDGPTRAGHDPMTFTYA
>NZ_CP026729.1|WP_033501502.1|2052692_2053436_+|HNH-endonuclease
MQRAGKRFKKSWINADGPLERILILLVVVAVVGVTIGMLLPKINPTVGEITGEYTATGTAAETLEKLTVDDNPSKAGYDRDAFGFRETDDDGNGCDVREDVLARDLTDVQYKNSRSCQVASGTLDDPYTGQTIQFVRGVKTSSAVQIDHVVALENAWQSGANTWDHTKLYQFGNDMYNLLAVDGPANQQKGSASAAYWLPTNSEYRCDYVARQIGVKDKYGLTVTTQEKRAMLSVLHGCPAQSVPER

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Crispr_ID: NZ_CP026729_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_5

2201886-2202062

Orphan

Consensus_repeat	Method
CCTCCACCCACTGGAGGAA	PILER-CR

3 spacers

The CRISPR arrays of NZ_CP026729_5

>merge|NZ_CP026729|5|2201886-2202062|PILER-CR
CCTCCACCCACTGGAGAAAAACACCCGCGTACCGGCCTCCAGACGTCCCAAAACCTCCAGTCACTGGAGGAATTGATACGTTGGCAGGCTTACAGCATCTAAATCCATCCACTCACTGGAGGAAGACACCCACTGACGGGCCTCCCAGCATCCAGATTCCTCCACCCACTGGAGGAA

>NZ_CP026729|5|1|2201886-2202062|PILER-CR
CCTCCACCCACTGGAGAAA	AACACCCGCGTACCGGCCTCCAGACGTCCCAAAACCT
CCAGTCACTGGAGGAATTG	ATACGTTGGCAGGCTTACAGCATCTAAATCCAT
CCACTCACTGGAGGAAGAC	ACCCACTGACGGGCCTCCCAGCATCCAGATTCCT
CCACCCACTGGAGGAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154304431.1\|2221338_2222703_-\|glycoside-hydrolase-family-27-protein	unknown	unknown	gnl\|CDD\|269893
NZ_CP026729.1\|WP_154304235.1\|2217886_2218843_-\|TatD-family-deoxyribonuclease	unknown	unknown	gnl\|CDD\|238635
NZ_CP026729.1\|WP_033501483.1\|2191741_2192851_-\|acyltransferase-family-protein	unknown	unknown	gnl\|CDD\|225813
NZ_CP026729.1\|WP_033501481.1\|2185154_2188181_+\|DUF4422-domain-containing-protein	unknown	unknown	gnl\|CDD\|379595
NZ_CP026729.1\|WP_154304225.1\|2197482_2197800_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|367091
NZ_CP026729.1\|WP_051920327.1\|2196928_2197483_+\|DUF4065-domain-containing-protein	unknown	unknown	gnl\|CDD\|226128
NZ_CP026729.1\|WP_154304233.1\|2215484_2217662_-\|potassium-transporter-Kup	unknown	unknown	gnl\|CDD\|376906
NZ_CP026729.1\|WP_033501482.1\|2188251_2189958_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304239.1\|2223015_2224119_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP026729.1\|WP_154304227.1\|2200891_2201248_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304429.1\|2199143_2200769_+\|sialate-O-acetylesterase	unknown	unknown	gnl\|CDD\|377084
NZ_CP026729.1\|WP_033501807.1\|2213481_2214273_-\|HD-domain-containing-protein	unknown	unknown	gnl\|CDD\|129396
NZ_CP026729.1\|WP_033501509.1\|2190064_2191663_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304228.1\|2210922_2212248_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|376899
NZ_CP026729.1\|WP_154304231.1\|2214399_2215284_-\|class-II-glutamine-amidotransferase	unknown	unknown	gnl\|CDD\|238889
NZ_CP026729.1\|WP_154304430.1\|2208353_2210714_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304230.1\|2212244_2213363_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP026729.1\|WP_033501484.1\|2193036_2193987_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|275035
NZ_CP026729.1\|WP_154304237.1\|2218964_2221322_-\|alpha-L-arabinofuranosidase	unknown	unknown	gnl\|CDD\|226064
NZ_CP026729.1\|WP_154304223.1\|2194055_2196659_-\|1,4-beta-N-acetylmuramidase	unknown	unknown	gnl\|CDD\|119376

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154304431.1\|2221338_2222703_-\|glycoside-hydrolase-family-27-protein	gnl\|CDD\|269893	cd14792, GH27, glycosyl hydrolase family 27 (GH27). GH27 enzymes occur in eukaryotes, prokaryotes, and archaea with a wide range of hydrolytic activities, including alpha-glucosidase (glucoamylase and sucrase-isomaltase), alpha-N-acetylgalactosaminidase, and 3-alpha-isomalto-dextranase. All GH27 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. GH27 members are retaining enzymes that cleave their substrates via an acid/base-catalyzed, double-displacement mechanism involving a covalent glycosyl-enzyme intermediate. Two aspartic acid residues have been identified as the catalytic nucleophile and the acid/base, respectively.	1.04995e-87
NZ_CP026729.1\|WP_033501483.1\|2191741_2192851_-\|acyltransferase-family-protein	gnl\|CDD\|225813	COG3274, COG3274, Predicted O-acyltransferase [General function prediction only].	3.28186e-18
NZ_CP026729.1\|WP_033501481.1\|2185154_2188181_+\|DUF4422-domain-containing-protein	gnl\|CDD\|379595	pfam14393, DUF4422, Domain of unknown function (DUF4422). This family of proteins is found in bacteria and archaea. Proteins in this family are typically between 255 and 371 amino acids in length.	1.10412e-83
NZ_CP026729.1\|WP_154304225.1\|2197482_2197800_+\|hypothetical-protein	gnl\|CDD\|367091	pfam02452, PemK_toxin, PemK-like, MazF-like toxin of type II toxin-antitoxin system. PemK is a growth inhibitor in E. coli known to bind to the promoter region of the Pem operon, auto-regulating synthesis. This family represents the toxin molecule of a typical bacterial toxin-antitoxin system pairing. The family includes a number of different toxins, such as MazF, Kid, PemK, ChpA, ChpB and ChpAK.	0.00295664
NZ_CP026729.1\|WP_051920327.1\|2196928_2197483_+\|DUF4065-domain-containing-protein	gnl\|CDD\|226128	COG3600, GepA, Uncharacterized phage-associated protein [Function unknown].	6.89963e-23
NZ_CP026729.1\|WP_154304233.1\|2215484_2217662_-\|potassium-transporter-Kup	gnl\|CDD\|376906	pfam02705, K_trans, K+ potassium transporter. This is a family of K+ potassium transporters that are conserved across phyla, having both bacterial (KUP), yeast (HAK), and plant (AtKT) sequences as members.	0
NZ_CP026729.1\|WP_033501484.1\|2193036_2193987_+\|glycosyltransferase	gnl\|CDD\|275035	TIGR04182, glyco_TIGR04182, glycosyltransferase, TIGR04182 family. Members of this family are glycosyltransferases restricted to the archaea. All but two members are from species with the PGF-CTERM/archaeosortase A system, a proposed maturation system for exported, glycosylated proteins as are found often in S-layers.	7.90259e-72
NZ_CP026729.1\|WP_154304239.1\|2223015_2224119_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.23372e-80
NZ_CP026729.1\|WP_154304223.1\|2194055_2196659_-\|1,4-beta-N-acetylmuramidase	gnl\|CDD\|119376	cd06414, GH25_LytC-like, The LytC lysozyme of Streptococcus pneumoniae is a bacterial cell wall hydrolase that cleaves the beta1-4-glycosydic bond located between the N-acetylmuramoyl-N-glucosaminyl residues of the cell wall polysaccharide chains. LytC is composed of a C-terminal glycosyl hydrolase family 25 (GH25) domain and an N-terminal choline-binding module (CBM) consisting of eleven homologous repeats that specifically recognizes the choline residues of pneumococcal lipoteichoic and teichoic acids. This domain arrangement is the reverse of the major pneumococcal autolysin, LytA, and the CPL-1-like lytic enzymes of the pneumococcal bacteriophages, in which the CBM (consisting of six repeats) is at the C-terminus. This model represents the C-terminal catalytic domain of the LytC-like enzymes.	4.46358e-69
NZ_CP026729.1\|WP_154304429.1\|2199143_2200769_+\|sialate-O-acetylesterase	gnl\|CDD\|377084	pfam03629, SASA, Carbohydrate esterase, sialic acid-specific acetylesterase. The catalytic triad of this esterase enzyme comprises residues Ser127, His403 and Asp391 in UniProtKB:P70665.	9.60421e-31
NZ_CP026729.1\|WP_033501807.1\|2213481_2214273_-\|HD-domain-containing-protein	gnl\|CDD\|129396	TIGR00295, Uncharacterized_protein_MJ0778, TIGR00295 family protein. This set of orthologs is narrowly defined, comprising proteins found in three Archaea but not in Pyrococcus horikoshii. The closest homologs are other archaeal proteins that appear to be represent distinct orthologous clusters. [Hypothetical proteins, Conserved].	5.87478e-14
NZ_CP026729.1\|WP_154304231.1\|2214399_2215284_-\|class-II-glutamine-amidotransferase	gnl\|CDD\|238889	cd01908, YafJ, Glutamine amidotransferases class-II (Gn-AT)_YafJ-type. YafJ is a glutamine amidotransferase-like protein of unknown function found in prokaryotes, eukaryotes and archaea. YafJ has a conserved structural fold similar to those of other class II glutamine amidotransferases including glucosamine-fructose 6-phosphate synthase (GLMS or GFAT), glutamine phosphoribosylpyrophosphate (Prpp) amidotransferase (GPATase), asparagine synthetase B (AsnB), beta lactam synthetase (beta-LS) and glutamate synthase (GltS). The YafJ fold is also somewhat similar to the Ntn (N-terminal nucleophile) hydrolase fold of the proteasomal alpha and beta subunits.	5.9231e-43
NZ_CP026729.1\|WP_154304230.1\|2212244_2213363_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	2.27185e-30
NZ_CP026729.1\|WP_154304228.1\|2210922_2212248_+\|FtsX-like-permease-family-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.	3.06194e-09
NZ_CP026729.1\|WP_154304237.1\|2218964_2221322_-\|alpha-L-arabinofuranosidase	gnl\|CDD\|226064	COG3534, AbfA, Alpha-L-arabinofuranosidase [Carbohydrate transport and metabolism].	2.5756e-30
NZ_CP026729.1\|WP_154304235.1\|2217886_2218843_-\|TatD-family-deoxyribonuclease	gnl\|CDD\|238635	cd01310, TatD_DNAse, TatD like proteins; E.coli TatD is a cytoplasmic protein, shown to have magnesium dependent DNase activity.	3.11452e-78

>NZ_CP026729.1|WP_154304227.1|2200891_2201248_-|hypothetical-protein
MAESDDELDIQRELDTRDSLASMARYHASSPSAITTQVLPPSFIPTATGRVRPVTGAFPAIQSDEQEKQSQLGRSVRSIRSLAAGSLRKSQDSTADGNDDDNNGVTPRMASSAPHYVD
>NZ_CP026729.1|WP_154304429.1|2199143_2200769_+|sialate-O-acetylesterase
MAILVAIIVGCGPKWGDGSANVNASNASSSSGTSDDSSANYATRASVQLPSYYMENMVFQRGKTLVVKGAVTTSQRGKTVDPTQLVTTISQGKKASSAQAKISNNGDFTCNLPKQKASLKPYSLTISYNEATLLTLKNVYVGDVFIAAGQSNMELNYSQYYEGPGNDYNFGGGLITTNDLPKQLSDKNVHFVASANTTEGTDFPLRDVNEQADSWLDATVDNSQHFSYLAQQFAMQLRAAHPNVPVGIVQTAWGGTPIRNHVKGGSIYANHIAPLEGFHVAGVLWYQGCNDSANEATALAYESQMTSLINQYRTVFDQNDLPFLYVQLARWPGYQYTQNVRFAQLSTLSNVGLHNASNVAMTVSLDTDKGTSTLIHPLGKDILGARMAAQYLAMSEGKAVPNGPLIAHAKHASDGTIVLSFQKGTATGLQAENPNYSKTASATVPNYTANSDATPLDGIANVATPTSASLQGFEIANDSGKWVPATAVINGKQIVLSAADGSSNLNAVTQVRYWWSGNPAISSLLYNDLGLPASPFIAVVE
>NZ_CP026729.1|WP_154304225.1|2197482_2197800_+|hypothetical-protein
MQPRPWQIWKVWFPFRENPSAGKYRPVVIKEVTEDNCVVIYITSQVEKTHFPDFMLIHNWDEAGLTKASAIRYRRMLKIPIDQLENYMGTLSPYDRIELQMKYLK
>NZ_CP026729.1|WP_051920327.1|2196928_2197483_+|DUF4065-domain-containing-protein
MLNVMDVADFFIATANEGDPEEDDGMTNMKLNKLLFFAQAASLQRFGKPLFDAPLEAWKYGPVVKSVYRTFKECQRDSIAKVAQPFDWQTIPPETLDLLCDVYRTYARDYSAMGLMRKTHQPDTPWSETYVPNENKVIPVESIQKWVQKQPLPIDMQPEPDKNIIVAELDSQGRPFLPEGWEDD
>NZ_CP026729.1|WP_154304223.1|2194055_2196659_-|1,4-beta-N-acetylmuramidase
MVSPHHVLKIATALSAVALTASVAVTPAYALQDIAIEDAVAQSGPVTADNGVVVQSDDQSDDQTGDQQSQDSMPDNPNAKLPDTVSDEISDDATVVSEDLAVTPEGEVKNIETGETVTDTTLVGTQDQQPDPLAKTNGESFIPVSAEDVKNAVADANVQLSKFESNEYGAHWGTYDNSKAFFDYQNNLFVQQAKGVIDVSEWQGDIDWAKAKADGVEGVIIRLGYGWGNNADKKAQRNISECKRLGIPFGIYWYSYADTPLIAKEEGADVVAKLKQFGVNPSDLAYPVYYDLEKWTWKGHQPPTDPNVYNDIVNNWYSALQSAGYKNLSVYSYTSYLQGPLKHADIYAKTTWVAQYGARMGFDSFPTDSRGWQYTSSGKVDGISGNVDMNAFGNKEFVNGGSSNDLQAAIDVRKMTAVTIPNGNYYINVRSKVTSSVDIPGGSAADSTAIQLYSGNGSKAQQFTFTRQSDGSYEIVNVNSGKALDVRNGVAESNAIVQQYSRNNSQAQRWFIRDSGAGYYLQSALGNWVLDLSGGNTADGAAIRLYTPNGTASQLFVVSSSDVNIATGVSMIITSVANKKLVTDVTSASTTNGARVQLYSSNNTNAQKYRFESIGNGTYKIVNINSGKMLDVAGGSTANGAALQQYTSNNTVAQQWTVRNYGSGKIALVSVNANKAVDIPGGNAVQQAQLQLYSPNGTVAQQWLVAKAPLTLRERLNETAAKHRQDLPDGTYTFGSKLNTSMKVDVSGASRSNYGNVQIWANNGTNAQKWKVTHDSSGYVTLTSVNSGKVLDVNGGVSANGTNVQQYDSNGTYAQKWIAVKNSDGSYTFQSALAENVVLDVNGGSSANGTNVQLYTSNGTNAQKWVK
>NZ_CP026729.1|WP_033501484.1|2193036_2193987_+|glycosyltransferase
MLEKNPNPSVAVLLPCYNEEVTIGKVVRDFKASLPQADIYVYDNNSTDRTAEIAAAEGAVVRREPRQGKGNVIRAMFEDIDADVYIMSDGDDTYPADAAPAMVDKILEGYDMVIGDRLSSTYFQENKRPFHNFGNRLVRGSINGLFGAHVTDIMTGYRAFSFTFAKTYPVLSRGFEVETEMTIHSLNNNLRLYEMPIQYRDRPEGSVSKLDTVGDGIKVMSTIFRMIREYKPLPFFGGLGLIVGIVGLILCGSVGIDFMRTGMVARFPTLIGAVMLVIAGLLLIVAGIILDVIAKNDRKAFIVDANHFALMKRRGK
>NZ_CP026729.1|WP_033501483.1|2191741_2192851_-|acyltransferase-family-protein
MGKRIVGYDVAKSIAMFFVVLLHFAFYTRYYSGGLAGTAVTTLCVICVPLFFAVNGALLLPRTFDVKKHYKKTCTVVAIVSIWKLLIAAFFVYVDGSHSVGVKNLVVFLFGGGFGEYPVGYFWFMNALIAVYLIYPLIKIAFDSNDKSAMGCLLAVIFVFSVGKDTVRVILQMLGSVSHHDFASVLDGVGQFYIFGDYGYVLMYFVIGGLIGASVSRSGGHCLDRFRLQPTVALLAVLLCYIVTFAIQRYQHAVQGTNLTVDHGYWLFPTFLATILVLQLLVNVKMEGGVAAVSKVVGANTFGIYMLHMIGLVLMSRLQVLPVFSCLGNMNSILVTLMNIVMALFVFLGCLIVSVLLRRIPVVGRLFSL
>NZ_CP026729.1|WP_033501509.1|2190064_2191663_-|hypothetical-protein
MFAFGDDASNSEGKILTLKTAFFYKALLFCLLFVFLFIAVDSAVEKMKWNALEENREARFLRYEWTIRSVLKNAVIIFICWFPYIFFLFPGVYWSDTSKQLLIHYGVEEFTDHHPFALTYLFGAFADFGEQTFGNPILGLYCLIVLQLITAIMLLSVTVLYTHKMGLSRRACHVELAFFALFPVFPVMFCSLAKDTISVLFLMAFCLLFVEVIRTKGDIATNPWVISGLFLCGLLTCLTKKAGVYVVVPSLVLAFLMVLSKKAKAILISVGMAVAVIMLILIPKCIMPALGVEPGGKQESIPFAIQQVAHDIKYNGDDMTEDEKGLVSDFLTIDYSKIADSYDPQIVDPVKGTKLKDESLFGDFIKLWIKKTVEHPLGHFESWIGLVKGWFGFQNNDGSPNYMVVCTESAWYYDPIMKYVPQWPVKASKSDMARSIYNMEQSVPVVNVLFSRSLWASILPCLMLFFALRPEKGKLGRVASMMPVDMSFVYLLLVPVSGMGGEPTRYVLQMICVAPLFLTLIAKSRSQENVEE
>NZ_CP026729.1|WP_033501482.1|2188251_2189958_-|hypothetical-protein
MTVVQKGMKRRVPLVVLAMICGFLASLVDSIRQNDQLVLAPRMLWYTLIIAILFFLFVLLLECVLAWLNREPETYRNVSCKLREIFSFKTSKKQFALIAVVLVLCWLPYLIVTYPGVIWYDTEQQLLQWNGQPNTFTNGSYLSDHHPVFDTMIFGTFLRLGAFFGSADRGLYLGCIVIELVTIASLASMILYCRHIGAGWRFCFAEMIFFAVFPFTALFSMTMVKDSLFMPFFIWFAMIFVEAVRTQGVLLKQPQFFTAFLLTALLMGLTKKTGVYIVLICCIILFFAVSSIIRKRAVGVFTVVISVFMILMPKIVFPVLRIQEGGKQEMLAVPLQQSALLVKRHENDVSRQDLEVIYKILGDDVADRYQWWASDNVKGYSWDSQNDQYLGQYAIAWIHGLASHPETYVEAYVALQEAWLGIPSPTDSNAGDLVMQTYALGSDHYALPDSVKLGLCFGGFKNAVQKLQETINDHIARAPIVNLLCSRAVWSTWIFVFVLYECIRRKQRHCSWLAPYVVTFLFLWISPATVTIEGMRYLIPMVMIAPLMLGMLGSGEQTNSAQAAEDER
>NZ_CP026729.1|WP_033501481.1|2185154_2188181_+|DUF4422-domain-containing-protein
MREKNPFFSIIIPCYNSASYIQECLDSLTKQSFTDWEAIVVNDASSDEASEIIEQYTSRDQRIHLLDKQINEGLHLARRSGVSISSGKYVLFLDSDDALAEETLSKVRFAINQNNPDIFRFGLTCVEQNGMNSHSAREFEAWANSPSSVSGGNQLLEDTFISPSEYGRDWHVTHKAFRGDICRRAFSVMSDTRLERAEDSYEFLVLASMSDLEISDTTIRGYIYNIGRGVTTDKSLSIQQFLTAANQMKLCWVAANAFAEDNQSALILKSSARLKERLIFSLMNDWKDRIPEKDKLEAAKQVSQVIGNTETSVELMRFVRDEAYTSLGYTNSSKAFVTWFKLAKSLVQDEPNIPARYLQLEKAASRHVKEYNAAQELYFRQENHRVKIFASTHKDVNRFPCDTIQMIQVGSSGNSMRLFYCHRDDEGENISDRNPRYCELTAQYWAWKNVDADYYGFCHYRRYFDFSDTPHKENPYGEIIDDYIDAKAAKEYGLDDTNIERVVHQYDVITTPFGDLTEIIDEHGTPRALWEAAPLLHDDDLLHCYRILCKMYPDYKEDADAFFKGNKACFCNMFIMKKEIFFDYCSWMFPILEEFDRNTDYSMYSKEALRTPGHLSERLLNIYLMHHKRIGSNWKFKELQCVHFTNPEPAEQLKPLDVTDKPIIPVVFAADDNYVPQLTTTVYSAMKNADPSYFYDVTVLQRNISWDKQERMRGFFKQFPNMNLRFTNVDRELAGYELSTNNAHISVETYYRFLIQKVLPFYDKVLYLDSDIIINGDIAKLYNIDLQGKLLGAVRDIDFLGNLNVKHGKRMNYAKTVLKMKNPYDYFQAGVLVLNTKAMRERYTIRQWLTYASNPAFIYNDQDVLNAHCESEVLYLPWEWNVVHDCGGRVGNLFVQAPNDIYDAYMRSRNNPQIIHYAGFQKPWTDPDCDFASIYWRYARETPFYERLLKRVVKATAPKAPVIVTPAKPPRAVGEDNPIRKIIDPIMPIGSRRRELLKSIGRTARGRR
>NZ_CP026729.1|WP_154304430.1|2208353_2210714_-|hypothetical-protein
MVAALATMESMTSEHITNTGSVMANHGSIQTPAQTQLRQDGSSNGGPSERKRDLRWRPAMLHPASLRVLLPWITSIIGIASALCLVIAWFPSTVWNTPIVSSDAPAHYYFIRRLLDEGLGAALHLWPHNSFYPPLFHVCAYFVIKIAALFGVQCSIYAAFNITWIIASGVMFPSGMLVLCRYFLQRWNRGNPISNLISRISQASPTSESSSVSESSNVSNQQVSSAVNRQYNATFVLQNLIGLFVPVFAVSSVCHPYGLLNAGPLIAFGFATSLLPFLIAATLRLFDAIAAREHIVKWLAITAIAGVVCLVAHPRIAFTYALILVPFIVLRLPWKLILGAFIAMCVGAVAFVALMLTSFKSDRWANPASWFHSHQPSKNLWESISFCFTDGLDGFPAILFALLLIAGTVAAFVCAFRRAAVRSSDSLSAAVSTVAPAFSVDALVSDAAVSLVSASDLPAASCSDAADVSLSAPSEPSRPRRNDRLRDVIALMAAFLLVTLVYVCTVTLVGALPNIISAPWYRDENRIMTMLPLVALPLLVIGVNALSECVSVCAASASFVPSASSFSAKNSASSVPSLSSASAVSSVKNVSFASNWIGPIAAFLVIAILAVSAQIVCPSRTAARDAIIAHSSLNQSDPNEQLTEQKITVLRKVMERTGTQATIISDPLNGSMYAETLFNASMLYPIINARTDVPSVPFGKVETAFASGDGQQVLGTVCPLTDAPEYFLTMGDQAQSLQSFPYRAQYDSFHNEELIDAYVDGGTLVKVADYSQYGQGWALYRFGCAD
>NZ_CP026729.1|WP_154304228.1|2210922_2212248_+|FtsX-like-permease-family-protein
MFVLKNAWAALGRVKWRTALIALLALLVSFSAAVDLAVIRADDTANNETYQSQKATAVIRPTAQTKAKRDGADSSYTDKYLTWEKYSTYATAAQSNSVTFDYTLAASVPVRESKSLQAIAAKSDISEDKTGGNLTLQAFYTLDAAKINDYGYYKVVKGKHLSYKTQSDGVLISQALADKNNLKVGDKVTVGNPSKASETYTFTVRGIYEYDSDVPEGNGSDAKYAKDNRENVIYTTYINFAKNGLDTTEATGWGVPNLNIVFSLANPSTYDKFVRSVKKAKLDTKTYEITSPSLTAYKKSIEPLDSAASSARIVLLAMTIIGGIALLALIVWAAVGGRRDEIGMAMITGVTKGRLGWQFMLETFMMTVPGWIIGLVAGALLAKPIGTAWAGGQAVAITSASIWNVIWYGLGTCLVLGIVAFVRVACFNLNQLFEERSEVTA
>NZ_CP026729.1|WP_154304230.1|2212244_2213363_+|ATP-binding-cassette-domain-containing-protein
MSDNMNDKNDNIDETVVDEAVVDQTAEAEASETVDDAAIGDIAADESSADSIESIDFTVVYDDDNAAVAGKDTADAAETADAANNAADTTNDDSDVAANNANQVKETLALRSSDAPTALETHEAVKADSATSVSSQLDNEIKRNRKKDEFFFKANPTFALDHVTVTNRKTGRNILDDLSLSFHAGATHAVLVDAEDREQHQALLATMVGMARTDRGNVMHKSANLSDVEPVEMLGHRIGFIPQRFAFRPDLDAESNVLYAMDASNRNFLKPKPAIARELLKRVGFDEVTSGLAVGEVSELNQRRVAIARALSCEAEVIIADEPTAGLDADDAAVVLDLLKKFKRDADRKRAIIVVTTNPEVADAMDHSVELD
>NZ_CP026729.1|WP_033501807.1|2213481_2214273_-|HD-domain-containing-protein
MTTGYIPTLAQVDELHRKIAQSQAAYDLIHGHCVVVADIARRMARRQNALFTRRCTLPDDAPEKAGNFGLRLTQDGNGSESFGMLRIPSVPSSDGLTGGTVPPRLIDEHLVVIGGLLHDIGTYFLLKQDGSDGGPLKFDGPNYVRHGLKGYEYLLNEGVDESIAQFARNHTGVGLTKEAVESQGLPLPPADYVPMNLEQEVVMVADKYNSKSIPPKFLTAEAYARKAARFGESNRREWLRLLERYGVLDVTPLAEQYHMRIAE
>NZ_CP026729.1|WP_154304231.1|2214399_2215284_-|class-II-glutamine-amidotransferase
MCRLLGFAAAGSNTSLNGVLGMQAVRDFRDLSEIHNDGWGSALVTVPSESPYLRDGGAPTPETGTAIYKNTIAARHDPIFDELANTPARGGLWHLRLASSNLPLILENQQPFYANGLSFIHNGDISDDQGRNIITNRAFPVDPSIVQSTGGRSDSAIFFAVILQYIGFGFALDEAVAQAVRELRKSYPKSSYNCMIQSQDQFIALCAAGREVTSKRIVEIYDQYGRGNQAHDYRVMRYRTLGESEADQAAGQPKGVVVASSGFDQCAEDGWTRLENDQMIIASNRTGAFRVRSI
>NZ_CP026729.1|WP_154304233.1|2215484_2217662_-|potassium-transporter-Kup
MANEPNEDEPLFHAATYTQAPKVSHKVLTKEERQVLIKQHEEKQQEAAHLDQVASKGPIGRWWSRLQSGPNRITPAMAIVALGVVYGDIGTSPLYTMQTFLNGQGGLAHADREAVLGVLSLVFWSITLITTVKYVLIAMRIDNKGEGGIFALYSLVRKYGAWLAIPAMLGGAAFLADSVLTPAVSISSAVEGLETLPAFEKLFTENKQLTLMITAAIILMLFSVQSRGTERIGKAFGSVVLVWFSFLAVVGLANLSQYWSVFAALNPVYGVRFLFSSHNAAGLAIMGTVFLSTTGAEALYSDMGHVGRGNIYFTWPFIKIALVLCYFGQGAWMLNHWDDSAYIRTHGLNPFFEMMTPSVRYVAVVLSVVAGVIASQALITGAFTMVSEATHLNWMPHLQVRYPARTRGQLYIPVVNVVLCVSTLLVLALFRDSEHISAAYGLALTITMITTTILLAVYIWHSGRRIGAVVFTVLFLAIQFMFFFASMAKFLHGGWFTMLLTFAILLVMYTWNEGTKLERAQRRHMQPAECLPVLKRLHDDDTIPYFADNIVYLTSDPETKRIDTDIFFSIFADHPKRARAWWAVSVETADEPFTREYSVENFGTDYMFRVRIRLGFKVSQSIPAYIHQIMNDLSKSGDLPRQESRYPKLDADPNIGPIRYVLIHKALMPESKVSQRGAISLEVKYAIRRLAGSPVKWFGLAPYNPLIEIQPLFLATQRPPRLKRV
>NZ_CP026729.1|WP_154304235.1|2217886_2218843_-|TatD-family-deoxyribonuclease
MSKHHRDRSWAPAPQPLPENAHVIDNHTHVASVVPFSRAMSHEAQEKGQPEVPVYSVDELLNQAQQVGVEGVIDCGCELPNLMTAIDMAREHPQTVHAAIAIHPNESVLHGHRGVPGPDGLPLKYKPWHDTSFEDAMAEVHRLAITYPNQVVAIGETGMDLFRTGEAAKELQREAFRAHIALAKELNLPMQIHDRDSHKEVIETLLADGAPERTVFHSYSGDAEMGEIAHENGWYLSLSGTSSYKGNDGIRESARIVGLSHVMVETDAPYLSPMPYRGRTNAPYMIPYTLQSLANYLDKPLTEVAQATRKTTREVYGI
>NZ_CP026729.1|WP_154304237.1|2218964_2221322_-|alpha-L-arabinofuranosidase
MDKLTAILNKAGVRNISTDLWGIFFEDISYSGDGGLNADLVQNGAFEYNRADSSDWSNYSFWRKIVPAGSFAAFDVLTDNPVAEENPHYASVEVEQAPASLENIGWDGMVFRAGETYDFSAWMRISSNCEASALPVTVALIDDDGNAIAEQDITVDSNDWRKQEVSLTVSGESNAIVVHEGALRLTFTTEGTVDLDFVTLEPRTTYNGLKHFRPDLVKALADLQPRFMRFPGGCITHGLGMDNMYHWDRTIGDVEHRPHNFNLWGYHQSFRIGYYEYLCLCETIGAKPLPVLPAAVSCQNTSQGPVPIVQKDMPAYIDEVLHLVEFCNGDAATTEWGAKRAAMGHPEPFNLEYLGIGNEDLIDDVFRNRFQQIFDAVKATYPDIVVVGTVGPAPSGPDYEAGWQYAREAGVPIVDEHSYQSSSWWFHNLDHYDTTDREGPKVYLGEYGSWNTQLINGLSEAAFMGRMELNGDAVVMSSYAPLFAKNGHHSWNPDLIYFDNERTYLPYSYWVQQMYATTTSDTAWPVAVEGKTTLRRELPPTVGLRLEGAAHADITNFSVDTADGRHVDLEDCHYAGNGPMNTSLNIDSDAYTINATITYYQGRWGLQLVHGDINGKNHNITSFGRAFEIKVVRDGTAYNLDGTEWSMDEVFPGTVWQVRIEVADRGESMKLYIDGELVAQGVEKPEEPRRTVTVARNDAEGVTYVRIVNALDAEAEIDLNQVLEELGVSAESRASATATVLAGTDPYAGEIGKASPTVPVGTAIDLTSGAYTAPSWSFTTLTLHD
>NZ_CP026729.1|WP_154304431.1|2221338_2222703_-|glycoside-hydrolase-family-27-protein
MGWNSWDSYGTTITEDEVLANARFMAEHLKAAGWDTLVIDAGWFDPNAHAHGYSDGTPLCIDEYGRQLPDERRFPSSAEGKGFGPLADAVHELGLKLGVHVMRGIPRQAVHENLPVKDTDLTARDVADTEHNCVWNHDNYGLKRGDAGAQAWYDAQVDLFASWGLDFLKVDDMQTPFFPEEIEAYHNAIAKAEKRYGRRITLSLSPGGWVASTHVDFLRDVAQMWRISDDLWDRWEDIFQQFPRLARWAPLQRTGHWADADMLPLGHIGLRAERGDDRQSRLTLDEQKTLLTLWCMGRSPLMVGGDLPTSDDDTIALLTNPALREVTAGSANNREIVRERLFSEWNVEDSYIGDLIVWTADAVKWADGTPCAHPGSHYGAIFWTGDEPYELKGNIQLQSFVGIADRNRDWTLADLWTDAPGTPSDIRIEGEGEDRVIRGTIPAHGALWFAIRPL
>NZ_CP026729.1|WP_154304239.1|2223015_2224119_+|substrate-binding-domain-containing-protein
MATSKPTLRDVAAAAGVSPMTASNALRGKTGVKESTRARVLAAAKKLDYRINLTASMLKSGRSNIIHVIVNEFDSPFYSKLTQALSNEIVARGLTPFIEQTRYSADAAAHALTSNPFSGQLFDGEILHATGLGTNLPLAKLNGGRPFVLVDACEETPTVDAVNFPNEEAERAAAQHLIDHGCRKIAIVGHAFTKRADLAHAQNAFLLRLRGACNALLDAGLPYDETTVFEAGSAEDGIAAGHAIAQQILATRGNADVGEGADPPFDGVCCANDFAAFGVIRGLADHGIRVPQDVQVIGFDGVTSGSYATPSLSTIEVDLNQLAKFVLDMIAERVERQGEEDAEPLPPSRATIGYQLVERESTAPHLL

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Crispr_ID: NZ_CP026729_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_6

2244466-2244566

Orphan

Consensus_repeat	Method
AAAATCATCCATTTCACTGGACG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP026729_6

>merge|NZ_CP026729|6|2244466-2244566|CRISPRCasFinder
AAAATCATCCATTTCACTGGACGATTCTGTATTTTCCACAAAATCATCCAGTAAAATGGACAATTCTGCAAAAATCGAAAAATCATCCATTTCACTGGACG

>NZ_CP026729|6|5|2244466-2244566|CRISPRCasFinder
AAAATCATCCATTTCACTGGACG	ATTCTGTATTTTCCAC
AAAATCATCCAGTAAAATGGACA	ATTCTGCAAAAATCGA
AAAATCATCCATTTCACTGGACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_033501799.1\|2227585_2229106_-\|sugar-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224053
NZ_CP026729.1\|WP_154304247.1\|2251811_2252879_-\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP026729.1\|WP_154304242.1\|2234864_2235629_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_099571530.1\|2245938_2246760_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223730
NZ_CP026729.1\|WP_003838378.1\|2225479_2226463_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|380660
NZ_CP026729.1\|WP_154304434.1\|2247005_2248136_-\|DUF2961-domain-containing-protein	unknown	unknown	gnl\|CDD\|378582
NZ_CP026729.1\|WP_033501798.1\|2229186_2230401_-\|anhydro-N-acetylmuramic-acid-kinase	unknown	unknown	gnl\|CDD\|236579
NZ_CP026729.1\|WP_154304249.1\|2255836_2257150_+\|carbohydrate-binding-protein	unknown	unknown	gnl\|CDD\|119360
NZ_CP026729.1\|WP_154304245.1\|2238785_2240573_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP026729.1\|WP_154304240.1\|2230626_2231670_-\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP026729.1\|WP_154304243.1\|2235736_2237902_-\|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl\|CDD\|226063
NZ_CP026729.1\|WP_162008514.1\|2240603_2242535_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP026729.1\|WP_033501800.1\|2226566_2227571_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224093
NZ_CP026729.1\|WP_033501791.1\|2248204_2249083_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP026729.1\|WP_154304250.1\|2257239_2259696_+\|EAL-domain-containing-protein	unknown	unknown	gnl\|CDD\|376350
NZ_CP026729.1\|WP_154304433.1\|2244621_2245827_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|224292
NZ_CP026729.1\|WP_154304248.1\|2253335_2255585_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|379305
NZ_CP026729.1\|WP_033501790.1\|2249151_2250090_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP026729.1\|WP_118270062.1\|2242939_2244028_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223730
NZ_CP026729.1\|WP_033501789.1\|2250255_2251563_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_033501799.1\|2227585_2229106_-\|sugar-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224053	COG1129, MglA, ABC-type sugar transport system, ATPase component [Carbohydrate transport and metabolism].	0
NZ_CP026729.1\|WP_154304247.1\|2251811_2252879_-\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	8.32455e-54
NZ_CP026729.1\|WP_099571530.1\|2245938_2246760_+\|alpha/beta-hydrolase	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	7.17289e-24
NZ_CP026729.1\|WP_003838378.1\|2225479_2226463_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|380660	cd20005, PBP1_ABC_sugar_binding-like, monosaccharide ABC transporter substrate-binding protein such as CUT2. Periplasmic sugar-binding domain of uncharacterized ABC-type transport systems that share homology with a family of pentose/hexose sugar-binding proteins of the type 1 periplasmic binding protein superfamily, which consists of two domains connected by a three-stranded hinge. The substrate specificity of this group is not known, but it is predicted to be involved in the transport of sugar-containing molecules and chemotaxis.	3.42098e-103
NZ_CP026729.1\|WP_154304434.1\|2247005_2248136_-\|DUF2961-domain-containing-protein	gnl\|CDD\|378582	pfam11175, DUF2961, Protein of unknown function (DUF2961). This family of proteins has no known function.	6.17643e-115
NZ_CP026729.1\|WP_033501798.1\|2229186_2230401_-\|anhydro-N-acetylmuramic-acid-kinase	gnl\|CDD\|236579	PRK09585, anmK, anhydro-N-acetylmuramic acid kinase; Reviewed.	1.95168e-118
NZ_CP026729.1\|WP_154304249.1\|2255836_2257150_+\|carbohydrate-binding-protein	gnl\|CDD\|119360	cd06543, GH18_PF-ChiA-like, PF-ChiA is an uncharacterized chitinase found in the hyperthermophilic archaeon Pyrococcus furiosus with a glycosyl hydrolase family 18 (GH18) catalytic domain as well as a cellulose-binding domain. Members of this domain family are found not only in archaea but also in eukaryotes and prokaryotes. PF-ChiA exhibits hydrolytic activity toward both colloidal and crystalline (beta/alpha) chitins at high temperature.	7.74119e-94
NZ_CP026729.1\|WP_154304245.1\|2238785_2240573_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.57618e-171
NZ_CP026729.1\|WP_154304240.1\|2230626_2231670_-\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	3.61925e-82
NZ_CP026729.1\|WP_154304243.1\|2235736_2237902_-\|glycoside-hydrolase-family-127-protein	gnl\|CDD\|226063	COG3533, COG3533, Uncharacterized protein conserved in bacteria [Function unknown].	1.44395e-179
NZ_CP026729.1\|WP_162008514.1\|2240603_2242535_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	8.59032e-173
NZ_CP026729.1\|WP_033501800.1\|2226566_2227571_-\|ABC-transporter-permease	gnl\|CDD\|224093	COG1172, AraH, Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components [Carbohydrate transport and metabolism].	2.82068e-86
NZ_CP026729.1\|WP_033501791.1\|2248204_2249083_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.87792e-65
NZ_CP026729.1\|WP_154304250.1\|2257239_2259696_+\|EAL-domain-containing-protein	gnl\|CDD\|376350	pfam00563, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues. The EAL domain is a good candidate for a diguanylate phosphodiesterase function. The domain contains many conserved acidic residues that could participate in metal binding and might form the phosphodiesterase active site.	1.67519e-25
NZ_CP026729.1\|WP_154304433.1\|2244621_2245827_+\|AAA-family-ATPase	gnl\|CDD\|224292	COG1373, COG1373, Predicted ATPase (AAA+ superfamily) [General function prediction only].	5.66015e-74
NZ_CP026729.1\|WP_154304248.1\|2253335_2255585_-\|glycosyltransferase	gnl\|CDD\|379305	pfam13632, Glyco_trans_2_3, Glycosyl transferase family group 2. Members of this family of prokaryotic proteins include putative glucosyltransferases, which are involved in bacterial capsule biosynthesis.	1.29237e-24
NZ_CP026729.1\|WP_033501790.1\|2249151_2250090_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.06195e-78
NZ_CP026729.1\|WP_118270062.1\|2242939_2244028_+\|alpha/beta-hydrolase	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	3.36632e-26
NZ_CP026729.1\|WP_033501789.1\|2250255_2251563_-\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.08882e-35

>NZ_CP026729.1|WP_118270062.1|2242939_2244028_+|alpha/beta-hydrolase
MADKQAIIAQYAEKYGLTDEMIKHAERWTETTVDLAGLSEARLQGILDMRFGAIAVDTPRSELWHTPDTIDVIEDIPYLPDGGYDTEAGQCRGHLLDLYLPHDAVLRCGHTLPVYIDIHGGGFTYGYKELNRNFNVHLAETGFAVFSLNYRPAPQTDLKGQLADVQAALRWIKAHLTDYPVNPNAVFLTGDSAGGALTMLTLAIENNAEAAAAFGIDEPSGIGFAGAAPVCGAYSSASLETMGSELTVGYDPNRRTGLEQMLGVEFFDGIEAADPKFLTAEGLAFNVDLPPLFIVTCGDDFLEADNLALAAALARKGADFELFDPKPRRHETLGHVFVIGMPWLDESVECFERLRRFSYERC
>NZ_CP026729.1|WP_162008514.1|2240603_2242535_-|ATP-binding-cassette-domain-containing-protein
MYVDPNRNKEAGNLKWILPYCKPDLPRVVGAIVLFCVNNTMALIIPLLSGLIVDRVIVQGHVSELTRLCIMMIVFTIVRVTSRYGYQMWMERFGQNSVFRLVSDEYEKLHELDFTYFNHTRTGDIMSRMTSDTDAIRHALSWVSYQVLDCVVMFVGALVMMFTIDWRLALALACVTPFIFILTRGLSTHARPLFFAIRNSLAEMNSMVEENIEGNRVVKAFVREPYETEKFDERNDDYMQRNMAQAYNSRKYMPWLDGLGFSLQLITLGLGGFLVITGRMTLGNLVAFNSYLWMIDGPVRQSGWLINDWQRFNASCIKIRKLLTSQSHITEKPGVGANANTATPNANNANGVNDATGNASQSQATFITSATQAAQATQVTTNTTRIAGSIDFQHVSFAFPDEPNTPVLEDVDFHVPAGAKLGILGETGAGKSTLVNLISRFYDPTEGSVLIDGVDARDWPLATLRSQVCVVAQDTFLFSDTIGGNISFGVGEQREYDEQYIRRMATIAGADGFIRSMPEGYDTVVGERGVGLSGGQKQRLSLARALADDPSILIMDDTTSAVDMETEAEIQRHLRELDEQKTIVTIAHRISSVKDSDLILVLEHGRIVERGTHDELVAAHGRYWEIYYKQLGLQAGRSHGFEA
>NZ_CP026729.1|WP_154304245.1|2238785_2240573_-|ATP-binding-cassette-domain-containing-protein
MAKRNTFREDEELEEQINLHDILRIGVYLKPYMSRIARILVVVVMMSCIAVVVPYLTKIMIDSAIPSKNLTLLGELTGLMAVLIVIYEFGLRYRTVEITRVGQLMLKDMRRDIFTHIQTLPFSYFDSRPHGKILIRVVNYVNTLSDTLSSGLINVISDVFTFLITLVVMFVVDWRLALFSLVLFPFLIAWVLMLQHFQRRAYQVLSNKQSNLNAFIHESIAGVKTTQTFAQEAAQFKTFQEQQNDVRTSWMKAVHIQFLMWPGIQTISVMTIAFIYYVGVTGFGAVNVSTGVLIAFVGYANNFWNPVISIGNFYNQLITCSAYLERIFETLDVQPEIRNAPDATELPQIEGRVDFNDVIFRYEPDGRNILNLVDLHVEPGSTVALVGPTGAGKTTIINLLSRFYDVAEGSVTIDGHDVRSVTLESLRRQMGVMLQDTFIFSGNVRENIRYGKLDATDAEIEAAAKAVHAHEFIMDLPNGYDTVVEERGSTLSAGQRQLIAFARVLLADPRILILDEATSNIDTRTEEALQAGLNHLLKGRTSFIIAHRLSTIENADMICYIDHGQIVEQGNHAELLAKRGAYYRLYDSQYAMIKV
>NZ_CP026729.1|WP_154304243.1|2235736_2237902_-|glycoside-hydrolase-family-127-protein
MTDIHNRHSHPIALRDATVTDPFWAAEQELVRTAVIPYQWNALNDNVPGATPSYCMHNFKAAAAQNAEHHKQGKAFVPPKYTFRGFEALPEDPANPDPDKFYGFVFQDTDFSKWIEAVGYSLTHHPDAELEATADAAIDIVCAAQLDNGYLDTYYILNGMDRHFTNLKDHHELYCFGHLVEGAVAYYEATGKRKLLDAACRFADYIDSRFGTEEGRLHGYPGHEIAEMALVKLAAVTGETRYAGLAEYFVRQRGQQPLYFALEDRRRAEEDGRNYEPREQNYAYYQADKPVTEQTEALGHAVRAAYFYSGVADVARITEEATLLESCETLWRNIVDRKLYITGGIGATHMGEAFSFDYDLPNDTAYSESCAAIALAFFARRMLEIQPKSEYADVMESALYNTTLAGMALDGKSFFYVNPLEVVPEACHRDERKFHVKPVRQKWFGCACCPPNIARMVESVQQYAYTVADDASTLYVHLYMGGVVSAKLGGSDVSLEVRADMPWNGAGAITVTLPSSDEGQVPESFALALRLPAWAGGESVADSIHAAGEKDSRITRTIRDGYLYLTGTWRDGDVIDFDFPMPVRMIAANPLVREDAGKVAFIRGPLAYCAEGTDNGDNLHLLHADAETIAADPDAVKVNEITFHAQAAAQDERGLGEVEPVDLPMVTLTIPAWRESSQGAADKSLYALWQPAQRQPTEVTLIPYFAWANRGETEMTVFLRS
>NZ_CP026729.1|WP_154304242.1|2234864_2235629_-|hypothetical-protein
MAVMKTRINMADGRHDDDYALSDEQKAAVAELSRSNVYAKQSKWKTLHELPIAEKWPYFKENFLSYAVIIAVVVVIVAAFGVSYLTKGPRAELSVEGINMGGYADQLDRLGSDFVKAEKISDSRLVQMDTSISLGDSENAQDGSARLLAMVSAGQINMIVTDADTFAEVNNRGDITKPAEIMGEAQLERIRGSLVDAKGNPVTDVKKAVGFDLSKSKVWKSVKGLPQQQMILGFSNVTKSKEMPVRFVEYLRFE
>NZ_CP026729.1|WP_154304240.1|2230626_2231670_-|substrate-binding-domain-containing-protein
MNTRPTLKDVGAAAGVSVYVASRALRGESGVAASTRARVERAASELGYVRNEMAAGLRKKNSHTVGILTASGRNQYYSMLAQVIDSTLREYGYYAVVSDMLKDRAGMGKPEEQSLRLLFEQRPAAIVATYALSKSALKIIESFHVPVVFVDSPSAVAGEWPFVGSDNRQAGKIAGDYLGGLGHKNIAAVSYPSSWPTCKARITGLREAAERCGADVTVVECDNNPESAYENMSRKLQESDGSSRCDAVFALNTMMAMGSFRALQENGFHIGRDISLIAMDDFDWAPMLTPPLTVISQNMDEIGRQAGRFVVDAIRGNALAGQNLIIPVRLIERRSCVNWNENTERSS
>NZ_CP026729.1|WP_033501798.1|2229186_2230401_-|anhydro-N-acetylmuramic-acid-kinase
MAYAIGLNSGSSFDGVDAVLIEINQAEDGSVLPPKYIDALSIDWPEDIQQQVLAAFDDTLGIFKLTRLNYVCGAVFAQAASELMKKHNLTGKDIDVIGYDGQTIYQEPPEHDQMKQYDASSPFYEMWTKYGYPCGLQIGEPGVVSVLTDAPVVTQFRSVDHTLQGTGAPLMQYFDYVLFRNDKPTATLNIGGISNCHVACADRSKMRAFDCGPGNVMIDQAMRVLYGKEYDANGEVAAQGTVNEEMLAEMLEHPFFKREIPRCAWRLDFGAEYTQSMLDKYANLSSEDKLATITAFSAEAIARAFSEFILPTGLGVDRLIASGGGVRNATLMKMIAERLPEGVKLETSDVIGIPPQYKEAIKFATIAFSTKRSIADNIPAACGATKFGVLGKLVLPPSQAKLTD
>NZ_CP026729.1|WP_033501799.1|2227585_2229106_-|sugar-ABC-transporter-ATP-binding-protein
MIDSTTDRTSLLLEVSNVTKKFPGVLALDGVSLKIRPGEVHALMGENGAGKSTLMKIIGGIHKANGGTITFKGQPYQPDGPADAQSKGVSLIHQELNLVPDLTVAQNIFLGREPMGKTGVFLSEEQAAAKADELLKSIGVTFSSKVLVRDLPVASQQMVEIAKAISFDSQLLVMDEPTAALTDREVDALFKLIHDFVSPTTAVIYISHRMEELMRISNRITVFRDGRFVKEVKTEETSRDEIVKLMVGRDITAYSRPSARVEGAPAAMSVRNITNAMVKDASFDVYPGEILGFGGLAGAGRTELARAIIGADSRSAGQVMVGGKTVDIRRPSDAVEAGIAYLSEDRKQYGLVLDKTIDDNVALASLKNYVNAIGWIRDTAIARTSKQYIDALSIKTPSSKQLVKNLSGGNQQKVVIAKWLARDCDVLIFDEPTRGIDVGAKQEIYELLDELAHDGHAIIVISSELEELLRVSDRILVMCNGSITGELDHSEATQENIMELATTFRK
>NZ_CP026729.1|WP_033501800.1|2226566_2227571_-|ABC-transporter-permease
MTSTNETLDMAKNSLRKRFNSNSLQQLLIFATWIVLLIGFSIADPHFMRMGNIVALLLASAVTGIQALGVTFTIATGGIDITPGLGMAMTGVITAMCMTAFHLPIWLAVLAGILSGAVLGWINGLLIAGFGVQPMIATLAMMLVAQGVALILSGSKPVYTTDEVGFDRIARGTQILGIPNAVWIFLAVAVISWIVLNKTRLGRYALSMGSNEEATRMSGVNVRRWKWAVYVLAGCFTGLSGVVMTSRLSAAQPATGSGYEMYAIAAAVIGGASLAGGRASITGTVIGALIITTINNGLQIMSVPDPWQKVFLGIVVIAAVLVDIYRQHNAKKAK
>NZ_CP026729.1|WP_003838378.1|2225479_2226463_-|ABC-transporter-substrate-binding-protein
MKKSKYIALAAVAAFTVAPLSACGAGQSNGSESKNYEIAMVAKGFSQSFWVSVHQGADDAAAKYGATVTFNGPDNDSQVDKQADMVQNAINKSPDAVAIAPLDEAALTPAVQSAKSASIPLFAFDTAFETNADAITSTVKTSNREVGKVAAENLIALLNGKGKYAVIAHSQTDATSTERRDGFLDYMKKNAPDMEMVGEVQYSNADQAKAQDIASAILQANPDLDAIFATNEATVVGAATPVESALKSGHKVLLVGVDSGKAQQQYIRDGVISGSVSQNPYQIGYKTIENAVKSLNGEKIDKVIDSGCFWYNADNIDDDDVQQAMYE
>NZ_CP026729.1|WP_154304433.1|2244621_2245827_+|AAA-family-ATPase
MVTSELIERPQYTDWLQRWKDRDVIKVITGLRRCGKSMVLELFRRSLVAKGIAESRIISINFESLDAHYPTDYQSLYDYIVERLQPNCTNYVFLDEVQHVEHFEKAADGLYVRDDVDLYITGSNANLLSSELATLLTGRYVELKMLPLSFSEYRNALQSTANDNALFDRYLTYGGLPYVTQLTEDRDIADYLGGVFNTILVADIAQRNPRMDMRAFNDVAAFLADNVGNLASLKSMSGGLAASGRRISPTTISGYIEEMVRNYLLFEATRYDLQGKAYLHSESKYYLGDMGFRFWLLGKRQGDLGHRIENVIYLELLRRYSTVSVGKLRGGEIDFVASDANGPHYYQVSQTVLDESTLARELAPLQTVRDNHPKTLLTLDTVGLGDYQGIQHRNILDWLLE
>NZ_CP026729.1|WP_099571530.1|2245938_2246760_+|alpha/beta-hydrolase
MKYFEHEILGIDGSAAKFVGYCLDNSEEIVPDRVRPSVLVIPGGGYEMTSDREAEPIAMQFLAAGFNAFVLRYSVKPSVFPVALLEAADAMKMIREHAAEWHVDPEAIAVIGFSAGGHLAANLATSTSDDVLEAHGYDPDAVRPNGLMLAYPVITSGTLAHRGSFDSLLGERRNDPEALESVSIERHIDTKTPPVFVWHTVPDEVVPYENTLMLIDACKKAGVSVEAHLFPNGGHGLSLGTAETAWQGVNGIEPSMQIWTQLAVAWMRRTFAR
>NZ_CP026729.1|WP_154304434.1|2247005_2248136_-|DUF2961-domain-containing-protein
MQVDSLGAFSARNPLDSLAVAAPGRTRCVNAENPTGGKGTAATAASALGPSRKGSPCIQTVKAGENVTLMDVDGPGVIRHIWMTVTDRTSPTGPNVLRNLILEFYWDGEETPSVQCPIGDFFCCGHAQACRVNSMPVVVVPNRGFNCYFSMPFEHARIVLRNDHNEDVPAFFYQIDYTEYDALPADTMRFHAQWRRERVTELARDYVVLDGVHGRGAYIGTYLALTALESRWWGEGEVKMYIDGDDQYPTWCSTGAEDYFGGAWSFADFDEHGRMHEQTFCAPYVGFPFYSQRLASHRESAYWDVNTPVTRGLYRWHIPDPIYFEHDLRVEWQQIGTEEGGNFERQDDVASVAYWYQLEPHTPFDPIGDRRFRQPR
>NZ_CP026729.1|WP_033501791.1|2248204_2249083_-|carbohydrate-ABC-transporter-permease
MTQTMTASAARKASKKTQHVRSTGDWITLIVLIAAALLVLFPLLVLTINAFKTPVDYNATGPLSLPKHFTMDGIISFWTTTKFPLKFWNSLIISLVVAAAAVVLSVLNSFALGIGRVKGNTWIVLAIMLANMMPQEALLYPLYTMFKQLGLYNTKLAIIIVFTIIQSAYGTYLLSSVYGTFPQAILEAAAIDGASRWQILRKVVLPISWPTISVLFVFFFVWTWNEYMIPMAFLMGDDVQTIPLALATLQGQRTMDATTLASASLLSIVPTIIFFIIFQRKLSQGITAGAVK
>NZ_CP026729.1|WP_033501790.1|2249151_2250090_-|sugar-ABC-transporter-permease
MSKKTKTGGVSMSRLPGNRSAKFVPYLIPGLVGLLVIVVIPFVWNIYLSFTRWRGVGPVKFVGLQNWKRLFADSTFWISFANSFWIIVAIVVIPTILGLFISSLLTDVIQKKFGGKTASFLRAMFYLPQLLPVAVAAIIMGWIFRPEDGAVNALLVKLGLGSLQHNWLGSPDSALPVLMFILVWIQLGYPIVIFMSGLQRVDPELYEAAGLDGANWWQKFRVVTLPSIIPELLVVILTATIGALKTFAPVYLLTKGGPGTATTVPSYYSYNQFFQVQQVGYGAAISTALTVVIIVFSIVFTMVQKHVEKELV
>NZ_CP026729.1|WP_033501789.1|2250255_2251563_-|extracellular-solute-binding-protein
MKITQGIALAAAAAMSLATLAACGSDTAQDAETPDSLSFWYYEEDDAGQTQAWRRAAEAFEKETGVEIKFERKSFTQIAQNGSQFLNSDEAPDLMESNRGNGSAGVLSTMGLLTDLGDYVSQYGWDKKVTGANAAVAKYDENGIMDGDTWYGMTSYAEFQRVYYNKDLFAKYGLEIPTTYDEFVEVCQKFVDAGVTPIAADAQEYGVMWLWWQLVSKNADAKFIDNWQLYKGDVDWNSKILTNSVNTINDWLDKGFISRNVTGMKAEDTTQAFIKGEYPIYQTGTWNQGRFVKQITTFDWDAAVMPESNFAIGCAGNLLVIPERSHHKDLAAKFIDYVLSDDVQNYLGNAGGIPVAGDVSKITDEKSKDMIEEYTSYANDGKLSYYPDYAASNLTDAVPAEFQELVNGTKKPADVLKGIHEKYDVGVEDMGVKTN
>NZ_CP026729.1|WP_154304247.1|2251811_2252879_-|substrate-binding-domain-containing-protein
MTCNANDLESRGRRKMAGIKDVAQEAGVSVSTVSYALSGKRSISAKTTDKVMAAVERLGYTPDASARKMRGMRNHIFALSAPIRGDINQAKYNAYFLQTAWQAKNRGYDVLLLTGEDAVADIRRVTQSNLVDGVVLLDIEERDERTAQAGSYSKPCVAIGYPAEHEGCACVDIDFAEAGRMAADCLYSKGHRNAMFLRDNETDYDRGSGYVLLFREALLERAKELGMTIHESSKHRDDRFDAAEFVRELRSSGERPTAIVNQANANVLKLVLQQLQASELRVPDDISVLSCGTYFEGELMPQPITEMPVMPQELCSKAVDLLVEAIDEHRDIKGLVELSTPVMHSRGSVTKVGDA
>NZ_CP026729.1|WP_154304248.1|2253335_2255585_-|glycosyltransferase
MVKIGGNEGGDRKHQWGAETSTQPLAIMHAKPSPTRVVLGYVAIACTVISWLVYMITMILSLFVNNPSLTLRFVVEGVLYMTIVTTLIFSALVYLTTRQGALYRFIRHERVPRAMLDDHFAHNYSKGITVLIPSYVEQPKVVEKTIWSAALQEFPDLAVVLLIDDPPHPKNDEARAILKASRELMPKVLAELAAPAERFTKARDETAATLANQMSARRSVVAHCAEDYRAAAQWLEHKADMWLIEDHTDNFFCDQVLRGLARDLRLTEQALNESITLQQHVDANRILQLYERLVRIFTAKGWSFERKLYASTSREGNKAMNLNSFIGLMGHSLKRVETSDGVILRDVREDESPDFVMRNSEYVLTLDADSMLLRDYCLRLVYQMEQPGNERVAVIQTPYSSYRGAPTRIERIAAATTDIQHMLHQGMTYYDATFWVGANAVIRKAALDDICVVSTEGTRTVKTYIQDRTVIEDTESSIDLGYFGWHLVNYPERLSYSATPPDFGSLVVQRRRWANGGLLIIGKFFRIVHARHQQGNDVTLGEWALRVNYMASIAWSSFGLMFLLAYPFDQRLLSPWVVFASLPYFATMSSDLKRNGYKRSDIFRIYGFNIVLLTVNLSGTLKSIQQGMTNTKIPFARTPKVNNRTASPALYVTMPWVIIIYSCMVFYADTFSHNWGNAVFAGFNAIVTFWALTAYIGIWHSVQDMVVGLIRWFFVPIKEPQQEAARKKSSWRDVLYFGDRQMIYESRPL
>NZ_CP026729.1|WP_154304249.1|2255836_2257150_+|carbohydrate-binding-protein
MMKPLFPGRRFSFLRLFIAILCIALVAAGTWSWITFTRTAAKKLPEPWFGGYVDVTTTPSYEFESKVGNVYRNVILGFVTAGDGCQPSWGGYYTLDEAASTLDLDSRIAQTYKTDRTVTVSFGGQNGTELAAACTDVDALANAYQQVIDRYHITSLDFDIENTNLDGYSETATRRAQAVAKLIANEKAKNKGKDDTSHDLIISLTLPADAEGLTAQGMQTVNAFLDAGVTLSTVNLMTMDFNVASTSITQSTLIKSSLNAAHAQYKTLLYSRGRLFSDHQIWELLGATVLIGQNDTKNEYFTLDNAREINTFALETSLGHLSMWSLNRDQQCGENYTNTNTLKTFCSGRKQTDGEFATTLGSGFRGTPGTLVDFDNTSWNSSQQAYPTWEPDVLYKQGDKVIWNGNIYESLGNNENEQPDSAEEGTNAPWRIIGPVL
>NZ_CP026729.1|WP_154304250.1|2257239_2259696_+|EAL-domain-containing-protein
MASKQSKHQATTGSHSRDGIRKPVRLTILAVIYTLFLAVAIAFHAQEGVQRLMEAPARICIWSLCFLLCLIYHKKRSSYRVAAEHTVLPPLTVILLVTGYFPDVAMFLIIVTIITSIITARSLKIGILHAGTTLAPIPLIKILFANTSHVLSIIISQNYVNAAINPYRFQHWLLPLLIMTVVVPIIRLICDIVTFFFAQIPIRKAMHEYSLSHILAMAVADLLAIVWIPEILEFANIGSDAATVLSVFMLALIAYSLLLMTVDTMSRLARSRSALKCIANVSDALPLPNQVPEETVVRRINRGLTHMRCFVSDANNLGKRGYSYRYSAPIFTGSRQYYLAMERSIWNRPFTSTDETILLTCGEVLAESLRVNKEVTLLRTESETDTLTGALTYRAFIGHLKSLQTENVHNLVAVVYFGVEHLRTVNEHYGRKIGNAVLRSVGMRLSQLLPNNVTLYRVNGAEFAMIVTDVTSTSDVEELATRMRNLAVMPVHTEEGEVSVDVSSSISFSNATDGFAVLLADASAHIYALESSNLPAVDGTTATLAAQNSSDDYVNASDVLRHAIEDNTISVLYQPIFDVNTKRITSLDTIVRVHDAKGRTLAPYFVTAEAHRLNMSVQLTLDVLETCVKDMTAFRQVAPELDIVDICMNGSELGASIFHERMEQLTHEQPQLRFGLQLGSHAIHVAHDEVDDEVADLAALPNVELGLTNAGTTYSEVAAFAHLPLDFVRFDKTVVRDFRTPRAKQIMQRTLDISRDNDAFHVVFDGVETLDQVEFIRSIGGTLAEGTLLSNAMSANEFLMRLETMGTALPEAAPRQAE

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Crispr_ID: NZ_CP026729_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_7

2262382-2262518

Orphan

Consensus_repeat	Method
GATTCTTCCACTCACTGGAAGATTCTGGAC	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP026729_7

>merge|NZ_CP026729|7|2262382-2262518|PILER-CR
GTCCAGATTCCTCCAGTCAGTGGAAGAATCTGAACCGCGAAATACCCTCGTACTGTCCAAAAACTTCCAGTGAGTGGAAGAATCATCCCGATGGCAGGCCGAAAAACGTCCAGAATGTTCCAGCGAGTGGAAGAATC

>NZ_CP026729|7|2|2262382-2262518|PILER-CR
GTCCAGATTCCTCCAGTCAGTGGAAGAATC	TGAACCGCGAAATACCCTCGTACT
GTCCAAAAACTTCCAGTGAGTGGAAGAATC	ATCCCGATGGCAGGCCGAAAAAC
GTCCAGAATGTTCCAGCGAGTGGAAGAATC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154304247.1\|2251811_2252879_-\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP026729.1\|WP_048349553.1\|2265512_2266454_-\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP026729.1\|WP_033501781.1\|2268074_2268779_-\|TENA/THI-4-family-protein	unknown	unknown	gnl\|CDD\|381693
NZ_CP026729.1\|WP_154304260.1\|2268951_2271057_-\|glycoside-hydrolase-family-2	unknown	unknown	gnl\|CDD\|225789
NZ_CP026729.1\|WP_154304248.1\|2253335_2255585_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|379305
NZ_CP026729.1\|WP_154304249.1\|2255836_2257150_+\|carbohydrate-binding-protein	unknown	unknown	gnl\|CDD\|119360
NZ_CP026729.1\|WP_033501814.1\|2274042_2274297_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304434.1\|2247005_2248136_-\|DUF2961-domain-containing-protein	unknown	unknown	gnl\|CDD\|378582
NZ_CP026729.1\|WP_154304262.1\|2273348_2273975_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_162008534.1\|2260924_2262232_-\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|238434
NZ_CP026729.1\|WP_154304263.1\|2274414_2275398_-\|16S-rRNA-(cytidine(1402)-2'-O)-methyltransferase	unknown	unknown	gnl\|CDD\|223390
NZ_CP026729.1\|WP_033501791.1\|2248204_2249083_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP026729.1\|WP_154304256.1\|2263433_2265434_-\|family-20-glycosylhydrolase	unknown	unknown	gnl\|CDD\|119335
NZ_CP026729.1\|WP_154304250.1\|2257239_2259696_+\|EAL-domain-containing-protein	unknown	unknown	gnl\|CDD\|376350
NZ_CP026729.1\|WP_162008515.1\|2259828_2260845_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|380486
NZ_CP026729.1\|WP_033501790.1\|2249151_2250090_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP026729.1\|WP_003835859.1\|2271270_2273133_-\|methionine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237029
NZ_CP026729.1\|WP_080789080.1\|2262552_2263365_-\|glucosamine-6-phosphate-deaminase	unknown	unknown	gnl\|CDD\|179028
NZ_CP026729.1\|WP_033501789.1\|2250255_2251563_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP026729.1\|WP_154304258.1\|2266936_2268061_+\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154304247.1\|2251811_2252879_-\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	8.32455e-54
NZ_CP026729.1\|WP_048349553.1\|2265512_2266454_-\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	2.08452e-48
NZ_CP026729.1\|WP_033501781.1\|2268074_2268779_-\|TENA/THI-4-family-protein	gnl\|CDD\|381693	cd19358, TenA_E_Spr0628-like, TenA_E proteins similar to Streptococcus pneumoniae Spr0628 and Saccharomyces cerevisiae S288C PET18. This family of TenA proteins belongs to the TenA_E class, and lacks the conserved active site Cys residue of the TenA_C class; most have a pair of structurally conserved Glu residues in the active site. TenA_C proteins (EC 3.5.99.2; aminopyrimidine aminohydrolase, also known as thiaminase II) catalyze the hydrolysis of the thiamin breakdown product 4-amino-5-amino-methyl-2-methylpyrimidine (amino-HMP) to 4-amino-5-hydroxymethyl-2-methylpyrimidine (HMP) in a thiamin salvage pathway; the role of TenA_E proteins is less clear. Arabidopsis thaliana TenA_E (not belonging to this family) hydrolyzes amino-HMP to AMP, and the N-formyl derivative of amino-HMP to amino-HMP. Members of this family include the putative thiaminase Streptococcus pneumoniae Spr0628, and Saccharomyces cerevisiae S288C PET18, a protein of unknown function whose expression is induced in the absence of thiamin. It has also been suggested that TenA proteins act as transcriptional regulators based on changes in gene-expression patterns when TenA is overexpressed in Bacillus subtilis, however this effect may be indirect. Many proteins in this family have yet to be characterized.	4.13002e-66
NZ_CP026729.1\|WP_154304260.1\|2268951_2271057_-\|glycoside-hydrolase-family-2	gnl\|CDD\|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	2.2787e-34
NZ_CP026729.1\|WP_154304248.1\|2253335_2255585_-\|glycosyltransferase	gnl\|CDD\|379305	pfam13632, Glyco_trans_2_3, Glycosyl transferase family group 2. Members of this family of prokaryotic proteins include putative glucosyltransferases, which are involved in bacterial capsule biosynthesis.	1.29237e-24
NZ_CP026729.1\|WP_154304249.1\|2255836_2257150_+\|carbohydrate-binding-protein	gnl\|CDD\|119360	cd06543, GH18_PF-ChiA-like, PF-ChiA is an uncharacterized chitinase found in the hyperthermophilic archaeon Pyrococcus furiosus with a glycosyl hydrolase family 18 (GH18) catalytic domain as well as a cellulose-binding domain. Members of this domain family are found not only in archaea but also in eukaryotes and prokaryotes. PF-ChiA exhibits hydrolytic activity toward both colloidal and crystalline (beta/alpha) chitins at high temperature.	7.74119e-94
NZ_CP026729.1\|WP_154304434.1\|2247005_2248136_-\|DUF2961-domain-containing-protein	gnl\|CDD\|378582	pfam11175, DUF2961, Protein of unknown function (DUF2961). This family of proteins has no known function.	6.17643e-115
NZ_CP026729.1\|WP_162008534.1\|2260924_2262232_-\|amidohydrolase-family-protein	gnl\|CDD\|238434	cd00854, NagA, N-acetylglucosamine-6-phosphate deacetylase, NagA, catalyzes the hydrolysis of the N-acetyl group of N-acetyl-glucosamine-6-phosphate (GlcNAc-6-P) to glucosamine 6-phosphate and acetate. This is the first committed step in the biosynthetic pathway to amino-sugar-nucleotides, which is needed for cell wall peptidoglycan and teichoic acid biosynthesis. Deacetylation of N-acetylglucosamine is also important in lipopolysaccharide synthesis and cell wall recycling.	2.91229e-128
NZ_CP026729.1\|WP_154304263.1\|2274414_2275398_-\|16S-rRNA-(cytidine(1402)-2'-O)-methyltransferase	gnl\|CDD\|223390	COG0313, COG0313, Predicted methyltransferases [General function prediction only].	3.85504e-102
NZ_CP026729.1\|WP_033501791.1\|2248204_2249083_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.87792e-65
NZ_CP026729.1\|WP_154304256.1\|2263433_2265434_-\|family-20-glycosylhydrolase	gnl\|CDD\|119335	cd06565, GH20_GcnA-like, Glycosyl hydrolase family 20 (GH20) catalytic domain of N-acetyl-beta-D-glucosaminidase (GcnA, also known as BhsA) and related proteins. GcnA is an exoglucosidase which cleaves N-acetyl-beta-D-galactosamine (NAG) and N-acetyl-beta-D-galactosamine residues from 4-methylumbelliferylated (4MU) substrates, as well as cleaving NAG from chito-oligosaccharides (i.e. NAG polymers). In contrast, sulfated forms of the substrate are unable to be cleaved and act instead as mild competitive inhibitors. Additionally, the enzyme is known to be poisoned by several first-row transition metals as well as by mercury. GcnA forms a homodimer with subunits comprised of three domains, an N-terminal zincin-like domain, this central catalytic GH20 domain, and a C-terminal alpha helical domain. The GH20 hexosaminidases are thought to act via a catalytic mechanism in which the catalytic nucleophile is not provided by solvent or the enzyme, but by the substrate itself.	2.35709e-88
NZ_CP026729.1\|WP_154304250.1\|2257239_2259696_+\|EAL-domain-containing-protein	gnl\|CDD\|376350	pfam00563, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues. The EAL domain is a good candidate for a diguanylate phosphodiesterase function. The domain contains many conserved acidic residues that could participate in metal binding and might form the phosphodiesterase active site.	1.67519e-25
NZ_CP026729.1\|WP_162008515.1\|2259828_2260845_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|380486	cd01544, PBP1_GalR, ligand-binding domain of DNA transcription repressor GalR which is one of two regulatory proteins involved in galactose transport and metabolism. Ligand-binding domain of DNA transcription repressor GalR which is one of two regulatory proteins involved in galactose transport and metabolism. Transcription of the galactose regulon genes is regulated by Gal iso-repressor (GalS) and Gal repressor (GalR) in different ways, but both repressors recognize the same DNA binding site in the absence of D-galactose. GalR is a dimeric protein like GalS and is exclusively involved in the regulation of galactose permease, the low-affinity galactose transporter. GalS is involved in regulating expression of the high-affinity galactose transporter encoded by the mgl operon. GalS and GalR are members of the LacI-GalR family of transcription regulators and both contain the type 1 periplasmic binding protein-like fold. Hence, they are structurally homologous to the periplasmic sugar binding of ABC-type transport systems.	3.21672e-81
NZ_CP026729.1\|WP_033501790.1\|2249151_2250090_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.06195e-78
NZ_CP026729.1\|WP_003835859.1\|2271270_2273133_-\|methionine--tRNA-ligase	gnl\|CDD\|237029	PRK12268, PRK12268, methionyl-tRNA synthetase; Reviewed.	0
NZ_CP026729.1\|WP_080789080.1\|2262552_2263365_-\|glucosamine-6-phosphate-deaminase	gnl\|CDD\|179028	PRK00443, nagB, glucosamine-6-phosphate deaminase; Provisional.	3.04458e-123
NZ_CP026729.1\|WP_033501789.1\|2250255_2251563_-\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.08882e-35
NZ_CP026729.1\|WP_154304258.1\|2266936_2268061_+\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	5.81359e-37

>NZ_CP026729.1|WP_162008534.1|2260924_2262232_-|amidohydrolase-family-protein
MEQSRERFANEVDIALAQSARPFAIHNARKVDAQGVAEHYWIVSDGSAIIATGNRDDDFAAACASVGLDADADSDSVSSVGSGDSMTGSVGSVTNAAGRMMTPGYVDIHAHGSWGSSFDDGVQGIRMARAGHMMHGTTRQVLSLITNPLDVMCANLQTVRGMMGARPDILGAHLEGPFLALSRKGAHDPECLKDPVPEYVDRLLHAANGCLRQITIAPELPHGIDAIRRFAAAGVVPAVGHCDADYATARKGFNAGAGIMTHMFNAMNGLHHREPGPIPAAVEDPRVTVELINDGFHVQDPMVRLGFGFAPHRIAFVTDAMAATDCPDGHYLLGALDVNVIDGHARLASNGAIAGSTLTLEKAVQRAVLELGFTPTDAVEAATLTPAKAFGFDRANPVTKQPLGLLAPGYAADVLLLNPATWAVEHVWCEAHLLR
>NZ_CP026729.1|WP_162008515.1|2259828_2260845_+|substrate-binding-domain-containing-protein
MATIREIAKRVGFSQATVSRVLKDDPTFSVKDSTREKILNASLEMGYKNVPQYQRITIPQNVAILDNVVPDEGLQDAYFDELREVLVKHAEEQLMNVTMQKDVDSLIANADKYAGFISIGPSPLDRKTLHRLHKKLPHGVFIDINPAPALFDSVQPDLEQTILDALDTLMTSGCSRIGFIGGLGNIMGEHEYPEDVRTFAFRNWALRLGLDVQELVYADGPFTVENGRLQGRQLVQDHADDLPDAVIVAADPLAVGVLQAFATENVMVPRDIKVISINNQEIAKYTSPALSSYDISQDELAKAAVLMLAEALTANRKISQHMRISTSLVVRDSFTPQD
>NZ_CP026729.1|WP_154304250.1|2257239_2259696_+|EAL-domain-containing-protein
MASKQSKHQATTGSHSRDGIRKPVRLTILAVIYTLFLAVAIAFHAQEGVQRLMEAPARICIWSLCFLLCLIYHKKRSSYRVAAEHTVLPPLTVILLVTGYFPDVAMFLIIVTIITSIITARSLKIGILHAGTTLAPIPLIKILFANTSHVLSIIISQNYVNAAINPYRFQHWLLPLLIMTVVVPIIRLICDIVTFFFAQIPIRKAMHEYSLSHILAMAVADLLAIVWIPEILEFANIGSDAATVLSVFMLALIAYSLLLMTVDTMSRLARSRSALKCIANVSDALPLPNQVPEETVVRRINRGLTHMRCFVSDANNLGKRGYSYRYSAPIFTGSRQYYLAMERSIWNRPFTSTDETILLTCGEVLAESLRVNKEVTLLRTESETDTLTGALTYRAFIGHLKSLQTENVHNLVAVVYFGVEHLRTVNEHYGRKIGNAVLRSVGMRLSQLLPNNVTLYRVNGAEFAMIVTDVTSTSDVEELATRMRNLAVMPVHTEEGEVSVDVSSSISFSNATDGFAVLLADASAHIYALESSNLPAVDGTTATLAAQNSSDDYVNASDVLRHAIEDNTISVLYQPIFDVNTKRITSLDTIVRVHDAKGRTLAPYFVTAEAHRLNMSVQLTLDVLETCVKDMTAFRQVAPELDIVDICMNGSELGASIFHERMEQLTHEQPQLRFGLQLGSHAIHVAHDEVDDEVADLAALPNVELGLTNAGTTYSEVAAFAHLPLDFVRFDKTVVRDFRTPRAKQIMQRTLDISRDNDAFHVVFDGVETLDQVEFIRSIGGTLAEGTLLSNAMSANEFLMRLETMGTALPEAAPRQAE
>NZ_CP026729.1|WP_154304249.1|2255836_2257150_+|carbohydrate-binding-protein
MMKPLFPGRRFSFLRLFIAILCIALVAAGTWSWITFTRTAAKKLPEPWFGGYVDVTTTPSYEFESKVGNVYRNVILGFVTAGDGCQPSWGGYYTLDEAASTLDLDSRIAQTYKTDRTVTVSFGGQNGTELAAACTDVDALANAYQQVIDRYHITSLDFDIENTNLDGYSETATRRAQAVAKLIANEKAKNKGKDDTSHDLIISLTLPADAEGLTAQGMQTVNAFLDAGVTLSTVNLMTMDFNVASTSITQSTLIKSSLNAAHAQYKTLLYSRGRLFSDHQIWELLGATVLIGQNDTKNEYFTLDNAREINTFALETSLGHLSMWSLNRDQQCGENYTNTNTLKTFCSGRKQTDGEFATTLGSGFRGTPGTLVDFDNTSWNSSQQAYPTWEPDVLYKQGDKVIWNGNIYESLGNNENEQPDSAEEGTNAPWRIIGPVL
>NZ_CP026729.1|WP_154304248.1|2253335_2255585_-|glycosyltransferase
MVKIGGNEGGDRKHQWGAETSTQPLAIMHAKPSPTRVVLGYVAIACTVISWLVYMITMILSLFVNNPSLTLRFVVEGVLYMTIVTTLIFSALVYLTTRQGALYRFIRHERVPRAMLDDHFAHNYSKGITVLIPSYVEQPKVVEKTIWSAALQEFPDLAVVLLIDDPPHPKNDEARAILKASRELMPKVLAELAAPAERFTKARDETAATLANQMSARRSVVAHCAEDYRAAAQWLEHKADMWLIEDHTDNFFCDQVLRGLARDLRLTEQALNESITLQQHVDANRILQLYERLVRIFTAKGWSFERKLYASTSREGNKAMNLNSFIGLMGHSLKRVETSDGVILRDVREDESPDFVMRNSEYVLTLDADSMLLRDYCLRLVYQMEQPGNERVAVIQTPYSSYRGAPTRIERIAAATTDIQHMLHQGMTYYDATFWVGANAVIRKAALDDICVVSTEGTRTVKTYIQDRTVIEDTESSIDLGYFGWHLVNYPERLSYSATPPDFGSLVVQRRRWANGGLLIIGKFFRIVHARHQQGNDVTLGEWALRVNYMASIAWSSFGLMFLLAYPFDQRLLSPWVVFASLPYFATMSSDLKRNGYKRSDIFRIYGFNIVLLTVNLSGTLKSIQQGMTNTKIPFARTPKVNNRTASPALYVTMPWVIIIYSCMVFYADTFSHNWGNAVFAGFNAIVTFWALTAYIGIWHSVQDMVVGLIRWFFVPIKEPQQEAARKKSSWRDVLYFGDRQMIYESRPL
>NZ_CP026729.1|WP_154304247.1|2251811_2252879_-|substrate-binding-domain-containing-protein
MTCNANDLESRGRRKMAGIKDVAQEAGVSVSTVSYALSGKRSISAKTTDKVMAAVERLGYTPDASARKMRGMRNHIFALSAPIRGDINQAKYNAYFLQTAWQAKNRGYDVLLLTGEDAVADIRRVTQSNLVDGVVLLDIEERDERTAQAGSYSKPCVAIGYPAEHEGCACVDIDFAEAGRMAADCLYSKGHRNAMFLRDNETDYDRGSGYVLLFREALLERAKELGMTIHESSKHRDDRFDAAEFVRELRSSGERPTAIVNQANANVLKLVLQQLQASELRVPDDISVLSCGTYFEGELMPQPITEMPVMPQELCSKAVDLLVEAIDEHRDIKGLVELSTPVMHSRGSVTKVGDA
>NZ_CP026729.1|WP_033501789.1|2250255_2251563_-|extracellular-solute-binding-protein
MKITQGIALAAAAAMSLATLAACGSDTAQDAETPDSLSFWYYEEDDAGQTQAWRRAAEAFEKETGVEIKFERKSFTQIAQNGSQFLNSDEAPDLMESNRGNGSAGVLSTMGLLTDLGDYVSQYGWDKKVTGANAAVAKYDENGIMDGDTWYGMTSYAEFQRVYYNKDLFAKYGLEIPTTYDEFVEVCQKFVDAGVTPIAADAQEYGVMWLWWQLVSKNADAKFIDNWQLYKGDVDWNSKILTNSVNTINDWLDKGFISRNVTGMKAEDTTQAFIKGEYPIYQTGTWNQGRFVKQITTFDWDAAVMPESNFAIGCAGNLLVIPERSHHKDLAAKFIDYVLSDDVQNYLGNAGGIPVAGDVSKITDEKSKDMIEEYTSYANDGKLSYYPDYAASNLTDAVPAEFQELVNGTKKPADVLKGIHEKYDVGVEDMGVKTN
>NZ_CP026729.1|WP_033501790.1|2249151_2250090_-|sugar-ABC-transporter-permease
MSKKTKTGGVSMSRLPGNRSAKFVPYLIPGLVGLLVIVVIPFVWNIYLSFTRWRGVGPVKFVGLQNWKRLFADSTFWISFANSFWIIVAIVVIPTILGLFISSLLTDVIQKKFGGKTASFLRAMFYLPQLLPVAVAAIIMGWIFRPEDGAVNALLVKLGLGSLQHNWLGSPDSALPVLMFILVWIQLGYPIVIFMSGLQRVDPELYEAAGLDGANWWQKFRVVTLPSIIPELLVVILTATIGALKTFAPVYLLTKGGPGTATTVPSYYSYNQFFQVQQVGYGAAISTALTVVIIVFSIVFTMVQKHVEKELV
>NZ_CP026729.1|WP_033501791.1|2248204_2249083_-|carbohydrate-ABC-transporter-permease
MTQTMTASAARKASKKTQHVRSTGDWITLIVLIAAALLVLFPLLVLTINAFKTPVDYNATGPLSLPKHFTMDGIISFWTTTKFPLKFWNSLIISLVVAAAAVVLSVLNSFALGIGRVKGNTWIVLAIMLANMMPQEALLYPLYTMFKQLGLYNTKLAIIIVFTIIQSAYGTYLLSSVYGTFPQAILEAAAIDGASRWQILRKVVLPISWPTISVLFVFFFVWTWNEYMIPMAFLMGDDVQTIPLALATLQGQRTMDATTLASASLLSIVPTIIFFIIFQRKLSQGITAGAVK
>NZ_CP026729.1|WP_154304434.1|2247005_2248136_-|DUF2961-domain-containing-protein
MQVDSLGAFSARNPLDSLAVAAPGRTRCVNAENPTGGKGTAATAASALGPSRKGSPCIQTVKAGENVTLMDVDGPGVIRHIWMTVTDRTSPTGPNVLRNLILEFYWDGEETPSVQCPIGDFFCCGHAQACRVNSMPVVVVPNRGFNCYFSMPFEHARIVLRNDHNEDVPAFFYQIDYTEYDALPADTMRFHAQWRRERVTELARDYVVLDGVHGRGAYIGTYLALTALESRWWGEGEVKMYIDGDDQYPTWCSTGAEDYFGGAWSFADFDEHGRMHEQTFCAPYVGFPFYSQRLASHRESAYWDVNTPVTRGLYRWHIPDPIYFEHDLRVEWQQIGTEEGGNFERQDDVASVAYWYQLEPHTPFDPIGDRRFRQPR
>NZ_CP026729.1|WP_080789080.1|2262552_2263365_-|glucosamine-6-phosphate-deaminase
MTEVIIVKNEREAGDIYGRSVADLIKTKPNAVLGLATGSSPLAAYQSLARIVRSEHIDVSQVRGFALDEYLGLPLDHPQSYHSTIHRTVVEPLGLNPDLVHVPGDVLDGAPLSDGERIAAAGPAYDRAIEEAGGIDVQILGIGTDGHVGFNEPGSSLASGTRVKTLVEQTRIDNARFFDDDINKVPTHCITQGIGTILKARHLVLLAFGSGKAEAVAETVEGGVSAFCPASALQMHPHATIIVDEEAASRLRHKDYYRYAYAHKPAWQRI
>NZ_CP026729.1|WP_154304256.1|2263433_2265434_-|family-20-glycosylhydrolase
MTNENTREWAIIPEPNSMTVGEGAVSLPYAGRVNESIAIGDGDYLLARQLVADIRSTTGLDWDYATGGMWPGFISLHIADSDASEEAGTPGAYTLTIDTDGIAITGYDFEGMRNGVQTLRQLIRQNGAILPVLQIEDAPAYQIRGYYLDATRGRVPTLAWLKQWADKLCLYKYNQLQLYIEHTFAFDGMSETWRGSSPLKPADILEFDQYCANLGIELVPSVSTFGHQYVAMRTQELRELGEFPEDADRPFSFIERMRHHTLNVADDRAFAFSTQLVDSYLQLFRTKRFNICADETFDLGKGQSKQEAQRVGVATLYATYVGKLCEHLSQQGHEPMFWGDIAIEMPEILETLPNNVTLLNWQYDPEATDEKIQLVAKAGAKQVVCPAVWGWNALLPRIDDAWNNIARIARYGLDCGAEGMLITDWGDFGHINDPRMAVPGMIFGAQYAWNPAGDSAGDTAENDLLARISRVEYDDCSARFVALLRNASAQAVFTWRELVEYLELDDGAGNCNTDVAQTIPCLTERLANQENALTLREARDRMMRNMATIIERVPQANRKLQQCMVEIAPIMAHIGKPGITAAVRIAMEGQLLLNRAGFALAEAHGVREAHDVDDRQPSDYRALARELECWCEAYAKEWAVTSQPSELHRIQETVWKAADELRRISK
>NZ_CP026729.1|WP_048349553.1|2265512_2266454_-|ROK-family-protein
MNARLHHNNRPQGCIGIDIGGTKIEGVLLDATDRVVDVCRMPSHSGENNVVTDIVRVARTLSNEPLPIGIGIPGQVNCATGQVRNVVNLGIETLELGERISEIMHVPVHVENDVNAAAVGATEFVEHVDGNATVVFLNFGTGLAAGLVRDGQAEHGYSGCIGEIGHLPVDPNGFACPCGQRGCLETVASGGAVAKLWPSANPPMPDLIRKARQGDEHANDVLGKVAHGMGDVIQIVAQAYDPQRIIIGGGMAKTGNDLIEVIQAELSRRAEGCRFLNTLDIASKIRIAAVDKPIGAIGAALAAKRAQLGNQTM
>NZ_CP026729.1|WP_154304258.1|2266936_2268061_+|ROK-family-protein
MSGTQAKASPSDIRISNITAAFEQLFPATQMSRANIGKLIGLSRFTTSEVTGEMVDNRILRELGPDNREGRGKRSQVLAIDTDCWRIASIDLSNPKLAKGALTDLSGRIVDRTELPADNGCSVDDVIGLCKQLIASTPLPILGIGIAVTGIVEPDGVVRKSVHLEWNELPLKAEVENATGVPTLVGNDTNAALVAERFFGDCSPNSMLISIGRGVGAALCLNDVIIEGSSSTAGEIAHVVVDPNGPTCECGKRGCLESLVSDDRLQERIAQDPASRTRILAEAGALLGRVMAIPAGLLDLRDISVYGAPEIVNAQFIDAMEDEIRRTMTTDYQKAPQIHRCRQGEDLTLRGQATIVIRTLVPTIHERGSLIGDA
>NZ_CP026729.1|WP_033501781.1|2268074_2268779_-|TENA/THI-4-family-protein
MTVNHVPEAPQSASGDYAWLGAEPGSVADQLYMSAADEWNQAINSRFVNEMLDDTLPESILKSYLIQDFKFFNQGIMSHAIELAPRQETKDMLAKQSQWFADNEATYFTGFLKEYGITDEEYNNSEQTPANREYCEYLTKLVQGTWEELITALCCMEWIYLAWAKRTIDAGVIQQIPAHKGWVDLHEGDHFRAWTGRLIALVNEYASVDGSEAEVFRTIVHLERRFFEDSYPQQ
>NZ_CP026729.1|WP_154304260.1|2268951_2271057_-|glycoside-hydrolase-family-2
MLDVKRVLKAAPTKMRSQEPLQQLWTPWGEQIASEWLSSNAAHKAFCPAKDGERKLENGRTPILNEHPRPTMVRSNHTMLNGFWDYAIVSIPESDNGPKWRKSATALTRDEAVQAVKETAIPETFDGKILVPFSPESALSGVHQTIYPDNMIWYRTIVHPVTLGGEEAVRQIGDANRLILHFEAVDYVCACFIDGQFAGVHVGGYLPFDVDISAFVDPDDDFEIALCVYDPNDSGTQMRGKQKIEREGIWYTAQSGIWQSVWMEIVPEAYIQTLTLKGAADGRLFIRAEIGGDKPNAKLRIVVTDPADGAIVADERFAAGMRKVRTEIATRSEHLWSPEDPYLYDVTATLEFGAAKSQEKQDVVRSYCAFRTVEIKPDLKGVARFHLNGKPLFLKGVLDQGYWPDGLLTAPSDEALIHDITAMKESGFNMLRKHIKIESARWYYHCDRLGMLVWQDAVSGGGEYNAWTTNRKPTLVRTTWNKYRDDTAKHFAALGADDSTYRRDWSRTCDAMVHMLAGHPSIVAWVLFNEGWGQFNACDAAERIHALDPTRPIDATSGWYDQRCGDFHSVHNYFRPLEIYPDKGPLRGYVAEYEKRHKRRRRAAHYAVLPVAQHGVRAFMISEFGGLAQLVADHAAVSRAYGYGEYDSIEDWRAAVRSVLASAESLESRGLAGYVYTQVSDVEEELNGLLTYDRRLNKFVQ
>NZ_CP026729.1|WP_003835859.1|2271270_2273133_-|methionine--tRNA-ligase
MSHILVNVAWPYANGPRHIGHVAGFGVPSDVYARYERMKGNDVLMVSGTDEHGTPILVEADKEGVSAQELANRYNRVIAKDLCDLGLSYDLFTRTTTGNHEQVVQELFKQCLANGYIYKGTQKVAISPSTGRTLPDRYIEGTCPICGADGARGDQCDACGNELDPDELLNPVSKINGETPRFEETEHFFLDLPALAEANLAWLKTREGWRTNVINFSIGLFKEVKPRAITRDIDWGIPVPVAGWIDNPNKKLYVWFDAVIGYLSASIEWARRKGDPEAWRAWWNDPETPGYYFMGKDNITFHSQIWPSEMLGYNGQGSKGGETGKLGPLNMPEQVVASEFMTMEGKKFSSSRGIVIYVKDILARYPVDAVRYYISVAGPESSDSDFTWAEFVRHNNEELAASWGNLVNRVANLMNKNFGEIPALDENEMTDEDRALLSETKAAFNTVGSLIENHRQKNALSEAMRVVGDINKYISATEPWKIKDNPARLGTVLHVAAQAVSDANHLLAPFLPHSAQKVWEALGGTGTFSPLPRLEEVEDLDKPGFMYPIITGDYKLGETVHPWASEPIVAGAPVPKPHPIFAKIPPEAVEEELARFDSELKARREAEAARLAAEKAKLEG
>NZ_CP026729.1|WP_154304262.1|2273348_2273975_+|hypothetical-protein
MDTSPPLLGNADLPGPMCLNLLASSGALCKLDSANAYSSHDSDTLYGRACIIATLLPSRSVACARTAAWVWLGGTFPDSIDIIAKAHYRTLRYGRKINVFNRVAPSEHTIKVGPITVTTPVRTACDLALNCVPETESKVSEIICMLMQEFHFRSNDCMQIMEDAKHIRNAPQARNYILAIDGRSYEHGNRKDCENRKNHKDAEYVRGA
>NZ_CP026729.1|WP_033501814.1|2274042_2274297_+|hypothetical-protein
MEPPSPPILLTPLVACSPGTAQDVLWHIAEYAPRLRKWLIANPSATPAMLEYLAQVGGPDVARSLQILLESLESRALDAIAHDG
>NZ_CP026729.1|WP_154304263.1|2274414_2275398_-|16S-rRNA-(cytidine(1402)-2'-O)-methyltransferase
MERMNERECEDKREREDENADGDAGLDALVSGANIPHGTVVLAATPIGNTADASARLIALLEHADIVAAEDTRRLYALANRLGVHVNGRVVAYHDHNERDKSDGLLDQVETGATVLVVSDAGMPTINDPGLAIVRRAIERGLPVTCAPGPSAVLDALCLSGLPTDRFCYEGFLPRKHSERVQYLRTLRSERRTIVFYETLHRIDEAMADLLDVFGPNRKMALCRELTKDFEQIRRGTVAQIRQSVIDEPPRGEMVLVVAGASEEEADAAVPASLSIEDLAVLSIDRAREDNLRIKDAISQVIAEHPLADGSLANRKQVYNTVLAMKE

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Crispr_ID: NZ_CP026729_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP026729_8

2326951-2327106

Orphan

Consensus_repeat	Method
TATTCAGCGCTCTCGACGGGCGCAAGCACGGCCTTGAAAAGGACTGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP026729_8

>merge|NZ_CP026729|8|2326951-2327106|CRISPRCasFinder
TATTCAGCGCTCTCGACGGGCGCAAGCACGGCCTTGAAAAGGACTGCTCGCTGAGCCGTCAAGCAGAGAGCCCAGTGGGCTCTCTGTAGGCGAAGTGAGAAGACGCGCTATTCAGCGCTCTCGACGGGCGCAAGCACAGCCTTGAAAAGGACTGCT

>NZ_CP026729|8|6|2326951-2327106|CRISPRCasFinder
TATTCAGCGCTCTCGACGGGCGCAAGCACGGCCTTGAAAAGGACTGCT	CGCTGAGCCGTCAAGCAGAGAGCCCAGTGGGCTCTCTGTAGGCGAAGTGAGAAGACGCGC
TATTCAGCGCTCTCGACGGGCGCAAGCACAGCCTTGAAAAGGACTGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP026729.1\|WP_154304316.1\|2330056_2332129_+\|sodium:proton-antiporter	unknown	unknown	gnl\|CDD\|223104
NZ_CP026729.1\|WP_055063865.1\|2333805_2334387_+\|dCTP-deaminase	unknown	unknown	gnl\|CDD\|234753
NZ_CP026729.1\|WP_154304319.1\|2332757_2333561_+\|esterase	unknown	unknown	gnl\|CDD\|223477
NZ_CP026729.1\|WP_154304308.1\|2323221_2324157_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224096
NZ_CP026729.1\|WP_154304307.1\|2322298_2323183_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223472
NZ_CP026729.1\|WP_048349547.1\|2350743_2351997_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238881
NZ_CP026729.1\|WP_154304296.1\|2313063_2313819_+\|NAD-dependent-deacetylase	unknown	unknown	gnl\|CDD\|238701
NZ_CP026729.1\|WP_154304312.1\|2325671_2326874_+\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP026729.1\|WP_154304301.1\|2317213_2319034_-\|alpha,alpha-phosphotrehalase	unknown	unknown	gnl\|CDD\|200472
NZ_CP026729.1\|WP_154304305.1\|2320476_2321892_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|224586
NZ_CP026729.1\|WP_154304310.1\|2324171_2325464_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|224567
NZ_CP026729.1\|WP_128832457.1\|2352824_2354042_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340874
NZ_CP026729.1\|WP_154304321.1\|2337238_2340145_+\|beta-glucosidase	unknown	unknown	gnl\|CDD\|366858
NZ_CP026729.1\|WP_154304323.1\|2347404_2350401_-\|HAD-IC-family-P-type-ATPase	unknown	unknown	gnl\|CDD\|223550
NZ_CP026729.1\|WP_154304299.1\|2315722_2316988_-\|threonine-ammonia-lyase	unknown	unknown	gnl\|CDD\|236182
NZ_CP026729.1\|WP_162008517.1\|2319415_2319649_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP026729.1\|WP_154304436.1\|2334909_2336352_-\|GHKL-domain-containing-protein	unknown	unknown	gnl\|CDD\|340412
NZ_CP026729.1\|WP_033501960.1\|2329499_2329949_-\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663
NZ_CP026729.1\|WP_033501964.1\|2352018_2352828_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223999
NZ_CP026729.1\|WP_154304298.1\|2313964_2315335_-\|DUF4143-domain-containing-protein	unknown	unknown	gnl\|CDD\|379306

Protein	Function_ID	Function_description	E-value
NZ_CP026729.1\|WP_154304316.1\|2330056_2332129_+\|sodium:proton-antiporter	gnl\|CDD\|223104	COG0025, NhaP, NhaP-type Na+/H+ and K+/H+ antiporters [Inorganic ion transport and metabolism].	6.09039e-80
NZ_CP026729.1\|WP_055063865.1\|2333805_2334387_+\|dCTP-deaminase	gnl\|CDD\|234753	PRK00416, dcd, deoxycytidine triphosphate deaminase; Reviewed.	3.54819e-92
NZ_CP026729.1\|WP_154304319.1\|2332757_2333561_+\|esterase	gnl\|CDD\|223477	COG0400, COG0400, Predicted esterase [General function prediction only].	6.82343e-20
NZ_CP026729.1\|WP_154304308.1\|2323221_2324157_-\|ABC-transporter-permease-subunit	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.30589e-69
NZ_CP026729.1\|WP_154304307.1\|2322298_2323183_-\|ABC-transporter-permease-subunit	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.44857e-66
NZ_CP026729.1\|WP_048349547.1\|2350743_2351997_-\|hypothetical-protein	gnl\|CDD\|238881	cd01844, SGNH_hydrolase_like_6, SGNH_hydrolase subfamily. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	3.51464e-46
NZ_CP026729.1\|WP_154304296.1\|2313063_2313819_+\|NAD-dependent-deacetylase	gnl\|CDD\|238701	cd01410, SIRT7, SIRT7: Eukaryotic and prokaryotic group (class4) which includes human sirtuin SIRT6, SIRT7, and several bacterial homologs; and are members of the SIR2 family of proteins, silent information regulator 2 (Sir2) enzymes which catalyze NAD+-dependent protein/histone deacetylation. Sir2 proteins have been shown to regulate gene silencing, DNA repair, metabolic enzymes, and life span.	1.65147e-93
NZ_CP026729.1\|WP_154304312.1\|2325671_2326874_+\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	2.32643e-30
NZ_CP026729.1\|WP_154304301.1\|2317213_2319034_-\|alpha,alpha-phosphotrehalase	gnl\|CDD\|200472	cd11333, AmyAc_SI_OligoGlu_DGase, Alpha amylase catalytic domain found in Sucrose isomerases, oligo-1,6-glucosidase (also called isomaltase; sucrase-isomaltase; alpha-limit dextrinase), dextran glucosidase (also called glucan 1,6-alpha-glucosidase), and related proteins. The sucrose isomerases (SIs) Isomaltulose synthase (EC 5.4.99.11) and Trehalose synthase (EC 5.4.99.16) catalyze the isomerization of sucrose and maltose to produce isomaltulose and trehalulose, respectively. Oligo-1,6-glucosidase (EC 3.2.1.10) hydrolyzes the alpha-1,6-glucosidic linkage of isomaltooligosaccharides, pannose, and dextran. Unlike alpha-1,4-glucosidases (EC 3.2.1.20), it fails to hydrolyze the alpha-1,4-glucosidic bonds of maltosaccharides. Dextran glucosidase (DGase, EC 3.2.1.70) hydrolyzes alpha-1,6-glucosidic linkages at the non-reducing end of panose, isomaltooligosaccharides and dextran to produce alpha-glucose.The common reaction chemistry of the alpha-amylase family enzymes is based on a two-step acid catalytic mechanism that requires two critical carboxylates: one acting as a general acid/base (Glu) and the other as a nucleophile (Asp). Both hydrolysis and transglycosylation proceed via the nucleophilic substitution reaction between the anomeric carbon, C1 and a nucleophile. Both enzymes contain the three catalytic residues (Asp, Glu and Asp) common to the alpha-amylase family as well as two histidine residues which are predicted to be critical to binding the glucose residue adjacent to the scissile bond in the substrates. 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 performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_CP026729.1\|WP_154304305.1\|2320476_2321892_+\|AAA-family-ATPase	gnl\|CDD\|224586	COG1672, COG1672, Predicted ATPase (AAA+ superfamily) [General function prediction only].	6.66736e-33
NZ_CP026729.1\|WP_128832457.1\|2352824_2354042_-\|MFS-transporter	gnl\|CDD\|340874	cd17316, MFS_SV2_like, Metazoan Synaptic vesicle glycoprotein 2 (SV2) and related small molecule transporters of the Major Facilitator Superfamily. This family is composed of metazoan synaptic vesicle glycoprotein 2 (SV2) and related small molecule transporters including those that transport inorganic phosphate (Pht), aromatic compounds (PcaK and related proteins), proline/betaine (ProP), alpha-ketoglutarate (KgtP), citrate (CitA), shikimate (ShiA), and cis,cis-muconate (MucK), among others. SV2 is a transporter-like protein that serves as the receptor for botulinum neurotoxin A (BoNT/A), one of seven neurotoxins produced by the bacterium Clostridium botulinum. BoNT/A blocks neurotransmitter release by cleaving synaptosome-associated protein of 25 kD (SNAP-25) within presynaptic nerve terminals. Also included in this family is synaptic vesicle 2 (SV2)-related protein (SVOP) and similar proteins. SVOP is a transporter-like nucleotide binding protein that localizes to neurotransmitter-containing vesicles. The SV2-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.03651e-22
NZ_CP026729.1\|WP_154304321.1\|2337238_2340145_+\|beta-glucosidase	gnl\|CDD\|366858	pfam01915, Glyco_hydro_3_C, Glycosyl hydrolase family 3 C-terminal domain. This domain is involved in catalysis and may be involved in binding beta-glucan. This domain is found associated with pfam00933.	1.09156e-36
NZ_CP026729.1\|WP_154304323.1\|2347404_2350401_-\|HAD-IC-family-P-type-ATPase	gnl\|CDD\|223550	COG0474, MgtA, Cation transport ATPase [Inorganic ion transport and metabolism].	0
NZ_CP026729.1\|WP_154304299.1\|2315722_2316988_-\|threonine-ammonia-lyase	gnl\|CDD\|236182	PRK08198, PRK08198, threonine dehydratase; Provisional.	0
NZ_CP026729.1\|WP_154304310.1\|2324171_2325464_-\|extracellular-solute-binding-protein	gnl\|CDD\|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	2.42927e-35
NZ_CP026729.1\|WP_154304436.1\|2334909_2336352_-\|GHKL-domain-containing-protein	gnl\|CDD\|340412	cd16935, HATPase_AgrC-ComD-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Staphylococcus aureus AgrC and Streptococcus pneumoniae ComD which are involved in quorum sensing. This family includes the histidine kinase-like ATPase (HATPase) domains of various two-component sensor histidine kinase (HKs) including Staphylococcus aureus AgrC which is an HK of the accessory gene regulator (agr) quorum sensing two-component regulatory system (TCS) AgrC-AgrA. The agr system plays a part in the transition from persistent to virulent phenotype. This family also includes Streptococcus pneumoniae ComD HK of the ComD-ComE TCS, involved in quorum sensing and genetic competence.	7.12391e-34
NZ_CP026729.1\|WP_033501960.1\|2329499_2329949_-\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	9.0803e-58
NZ_CP026729.1\|WP_033501964.1\|2352018_2352828_-\|alpha/beta-hydrolase	gnl\|CDD\|223999	COG1073, COG1073, Hydrolases of the alpha/beta superfamily [General function prediction only].	8.74457e-09
NZ_CP026729.1\|WP_154304298.1\|2313964_2315335_-\|DUF4143-domain-containing-protein	gnl\|CDD\|379306	pfam13635, DUF4143, Domain of unknown function (DUF4143). This domain is almost always found C-terminal to an ATPase core family.	8.4602e-36

>NZ_CP026729.1|WP_154304312.1|2325671_2326874_+|ROK-family-protein
MAVSPLPQWFEGSEYTHKVATCVMKYGPISRITLAQILGLSQGAVSRITSDLIYAGVIEETPMPSGKAGKLPKGFVQKENAERRGRPQTGLRIIENARSFVGMKINATHISAVAVNAIGQIITGCHDLEIEDTSPQAVVALIKQLTIDCSDEAEMAGWPKPCAVGISLGGHIVDNAVVTFAPFMHWSQPVELSAMVREATGLPTGIYNDIDSLVVDACMFGSGVGLNSFAVLTFGAGVGYSLTVNGELVNCPDKSYGLVGHILVDPDGPRCVSGHKGCAQCLSDNSIAAEYSQIIGHPTSFDDFARDARANKPQATNLVNRTCFRLGTMVATIANLAMPDKIMIAGESSFIAKFGIDDLRNGINMYRHSQAAPVDFEIPDHDWALWAKAAAAQAIRQYVG
>NZ_CP026729.1|WP_154304310.1|2324171_2325464_-|extracellular-solute-binding-protein
MKPDSTTSVGKFRRIVYRTLTAVCAAALTAGLAGCGNSTAGTVTLDFFQFKAEAADWFTAKAKEFEKTHPNIKVNVNNSSDATTDLRTRLVKNREPDVITINGDINFGMLAEAGVFHDFTDDDIVDELNPGMVNIAKSLVQTNDKSKKRLYGLPYAGNASGYIINADVWEQAGEDPDNPPQTWSEFIDLLQRFKSKGIVPIEASTADSWTLQAPLASLNSTLVPESEYLSLKDGSKKFSDLWGTVSDQLVEIYQNYTQKNPAVTYQQATQDLAAGKAAILPLGTYAIPQIRLINSDANLRFAQMPATDNAEEQQLTAGDDVILTMGAHTKHEKEAREFIDFLMNDENIKDYSKRQSAFTPYKDTYVGDEALNGVLDFYRAGKLADFCDHYVPASINLAGFLQTLIQSGNTEKFLNGMQSEYDKIEARNFR
>NZ_CP026729.1|WP_154304308.1|2323221_2324157_-|ABC-transporter-permease-subunit
MTTAHTANTAKKSAKTSKNKVSKYSKRKVDPAFYWMTVPAVILVSIFLYWPFLQGAAYSFTNSQGYGDFKFIGLKNYIAMFQDSRVGHAYLFTIFIAVLITIGTNFLGMFLAVLLNSKIAFKNGFRAIFFIPYTLSVLVIGYVFKYIFMTPLPAIGQALHIDWLSTSMISNPDLAWFPIVFLSIWQGVAYSTLLYLAGLQTIDNEIYEAAAIDGVNAWQNFWQITFPLIGPFFTINMVLSLKNSLGAFDQIMALTKGGPDSKTETVSYLIFQNGLGNGEYSYQMANAVTFFIVLAILAFVQLKFFSGKEKV
>NZ_CP026729.1|WP_154304307.1|2322298_2323183_-|ABC-transporter-permease-subunit
MTSVTVAKTAKTGVQAQAKPEKIRRDHKVNWWLTAVVAVLSLTVLVPLYFAVVTALKTPGEAGTFSLPITWEWHNFADAWNKVNYPKAALNSAIITVCAVVLTLLTNTFVAYAVARNMDKRFFRFLYYFFLAMMFVPFTVIMLPIAKEMGSLHLDNQLGLIILYTILGIGTNLFIAIGFIRSIPISLEEAARIDGASTWRIFWTIIFPLMGPINATIAILTALWAWNDFLLPLITLTDQSNQTIPLAQYVFQSQFTSNYPMAFASYLMAMAPVLIVYIFAQKRVVGGVMRGAVK
>NZ_CP026729.1|WP_154304305.1|2320476_2321892_+|AAA-family-ATPase
MFVGRKQELATLEQQFSRHRFEMTVIYGRRRIGKTALIDQFVANKKTLYFTALQRSSAINLHLFTIQIANFFGLPTLPDFTDWYSALQFIIAQAKTLNERFVFVFDEFPYAALMSESLPSEMQIAIDHGFKDLNCMIILSGSNEGFMESEVLGYKSPLYGRRTSQIRLQPLNYTAIGEFVPQSSVFDRINYYATFGGTPYYLTQLDPDADFETNVLNLCFNQLGLLHEEPMMLLREELREPALYASVLQAIAGGSSTPKIIAEHSGVDPNSINKYLRILEELGLVSRNVPFGERPEKSRKALYSIKDPFFAYWYQFVAPAQSAIESHAGQNAARQLAFNDAFTTYVGQQFEVICLQWLLKHNGENGENCAVPFLATQFGKWWGNDPRKREQTDIDIVLGNPQTKQLLMCECKWRNTLKETEAVEALRDRVGLIRGYGETHLMFFSKYPISDATQRKYEGQVTFISAEQLFA
>NZ_CP026729.1|WP_162008517.1|2319415_2319649_-|hypothetical-protein
MPARNSSSVCFDVNVTVPDNAVMAAKSACPWNGVRVDASDVRVQRLINTSLHDLDGLRMSIPALPEDRFLAVDDFMI
>NZ_CP026729.1|WP_154304301.1|2317213_2319034_-|alpha,alpha-phosphotrehalase
MTDFNRSILPDAVRSNGATPNPWWANAVVYQIYPRSFQDTNGDGVGDLKGITSRLDYLADLGVDVVWLSPVYRSPQDDNGYDISDYQDIDPLFGTLEDMDELLAEAHRRGLKIVMDLVVNHTSDEHAWFQASRDKDDPHADWYWWRPARPGHEPGTPGAEPNRWGSYFGGSAWQYDPKRGEYYLHQYSRKQPDLNWENPEVRKAVYRMMNWWMDRGIDGFRMDVITQVSKTVDKNGKLPGEDGSEIEDYPVGEEGYSSPFSWCSDGPRIDEFLAEMRREVFEGREGYMNVGEAPGITPDRNEFITDPKNGELDMLFLFDHVGIDQEGSKWNTVPFEVRNLRTRLAAQQEAVKDAGWASLFFCNHDQPRVVSRWGDDSDRESRELGAKAFGMLLHMHRGTPYIYEGEELGMTNAHFTSLDQYRDLEAINAYRQRVEEARCQSPESMMAALALIGRDNARTPMQWDASRYAGFTAPDAAAEPWIGVNPNHVEINAAEEFDDPDSVYGFYKKLIAMRHNNATVATGEWNLLAADDEQVYAFTRTSGDDTILVVVNLTDKSAGLPGEVAELLGDGVAESQTLLSTYDVAHSVKSIARGELARWEGVVIQL
>NZ_CP026729.1|WP_154304299.1|2315722_2316988_-|threonine-ammonia-lyase
MEQNEVLKALQRDHAAELKLAAERLKGTARHTEIIPSKVLSDMTGHEILLKPENLQVTGSFKIRGAYNKIASLSDEQLARGIVTASAGNHAQGVAYAARERGAKATICMPQITPPLKVDATKAYGADVVLYGEVFDESAARAQELSDTEGMIYVPPFDDYEVLCGQGTIGLEILEDVPNVTDVVVPLGGGGLGAGVALAIKTFKPEVRVIGAIPEGSPAWKNSLAAGHVVAADQVRTSAEGVAVKRPGDLTFALLNEFLDDIVTVTERDINEMILLMLEKHKLVVEAAGAVSLAALEHLNLRSRKFAEAKGPHVVVPILSGGNEDTVSISAVIQKGMIARGRIMNFEVELPDIPGQLVKVATILAEQRANVIALDHDQFKASSHYTDSVSLGVTVETNGPEHIDRILDAMREAGFQPKRIY
>NZ_CP026729.1|WP_154304298.1|2313964_2315335_-|DUF4143-domain-containing-protein
MTENSNQQVKPQGYRPRIVDQQIERYMRIFGAVEIAGTKWCGKTWSARQHAASITYVDHSNNLMAAQSDPSLMLLGERPHVIDEWQLVPPIWDEVRHKVDDEPGEKGQWLLTGSSTPMHDKRPKHTGAGRIGHVRMSPMSLFESGDSTGEVSLSSLFEGDFNPAKVETPTERLFDFVCRGGWPEAQNLPVSDAQILIREYVHLTLNEGVSRQGRDPEVARRLLRSLSRNVSQSVTFKTLGLDMYGAELDLDSDVADKQNDSQKKDLQKDLEDFISPRTISEYVAMFERMFVIDGVPGWVPPSRSPKRLQTKPRRYFADPSIAAAVLGVNPRALLEDWQTFGFLFENLCVRDLLVYARALPDIGDEPVRYYHDDSGLECDAIIELTDGRWAGIEIKSSQSKVDDAAKNLLRLREKLLKNPQSRVRAPEFLAVLVGVGDFAYQREDGIYVIPITALGA
>NZ_CP026729.1|WP_154304296.1|2313063_2313819_+|NAD-dependent-deacetylase
MSKKIAVLTGAGISTSAGIPDFRGPDGVWTKHPEQTKVYDIDAFLANEEDRVYSWRWQKESPVWNAQPGTSHKALVKLEQAGLLTLLATQNFDALHEKAGNSSDVIVNLHGTIGTSHCMKCHAKYDTADIMANLDNEPDPHCHRRLPYSGNMPCNGLIKTDVVYFGEALPDGALEKSYRLATQADELWVIGSTLEVMPAASIVPMAAQAGVPITIMNMGRTQYDRLADRLIHDDIAVALPQLVDETIAAAQ
>NZ_CP026729.1|WP_033501960.1|2329499_2329949_-|nucleoside-deaminase
MQWSDDMGLAIELAREAAAEGEVPVGAVVLDAGGAVIGRGRNLREAHADPLAHAEVKAMTQAARSLGTWNLADCTLIVTLEPCPMCAGACLQTHVGRIVFGAWDAKLGACGSIWDIPRDPHIGHVPEVIGGVREAECARLMTDFFAGKR
>NZ_CP026729.1|WP_154304316.1|2330056_2332129_+|sodium:proton-antiporter
MAVFELIVCIIAAVVLSSFISRFIPKVSTPLVQIALGALASQLPFFPNVTLDPELFMVLFIAPLLYLEAHEIDKSELLKSVKLSLSLAIGLAIATMVAVGFTLHAAWPAIPLAAALALGAALGPTDAVAVSSLGKEAALTQRQTSVLKGESLFNDASGIVGFQFAIAAAISGVFEVGDSAIQFVFSFFGGAIFGLAVGMIADLLFESLRSFGWETTTSRILMELFLPFILYLGAEAVHVSGILSVVTAGLIIRFDRTGIGPNVARTNIVSSSVWGVFSFTLNGTVFILLGMLLPNAMSASWDDPQVSNWRLLVAILTVSAVVIVMRFLWISLMLRLARDTVTGKRRKMTAQRWRSAAVMTFGGPKGTITLSLMFTIPYTITGGAWFPMRDELIFIAGGVIVVTLLLANFLLPLLAPNRNKDASVEMTEITIEVLRRTVEELTGRVTPDNRRAVLMIIDSYTKRITRLKQRIGEIDPQGYMQLQIDALNWEKEYVKTRLAKVKATPNDDKAAHDLEIEACERLLDQIMSSLRHIETEHNSGRTIWRAKGRFRALQRRMGTMLKRVNSRIRRTTPLFSDDELFAHTRVVQVDAIEHVIDRLYEEMGRDTYNTEHCSALLLDYRRGEATLRSRPNVGTSAEAQAQAEDVKRESYGIELGVIQDMYEAGDITRAQSKQLRRNVYVMSVDADAQI
>NZ_CP026729.1|WP_154304319.1|2332757_2333561_+|esterase
MSEIREHETSDSYDSNNPGTPTGLIGRESPVIPGRFGEPLQVTHVQYSRGGGSAAPRRPLFLCLHGWGSNEADLADMMRYVAPYNDFASLRAPLVLQEAGSGEFGFGQGAYSWFHDCVPSGEDLDRDAYAAAQAIDDWVARNVSEDRAVVPIGFSQGGLLAIQLLRVHPERYAASISLSGFLAPGIIAGSAPADSHVAELNIPVFYGYGKNDTVIPMPELFATAAWLDEHTFLTSKSYRGLDHAVSLNEFSDLRDWLAAHDIAPGIL
>NZ_CP026729.1|WP_055063865.1|2333805_2334387_+|dCTP-deaminase
MLLSDRDILAAQAEGHISLDPWTPEMVQPASIDVRLDRFFRLFNNHAYTYVDPAENQGELTEQFEVAPGEPWILHPGEFALGSTWEYVKLDPTIAARLEGKSSLGRLGILTHSTAGFIDPGFEGHITLELSNVSTLPVKLWPGMKIGQMCFFQLSSPAEHPYGSQGTGSHYQGQRGPTPSRSYVNFYKADIAD
>NZ_CP026729.1|WP_154304436.1|2334909_2336352_-|GHKL-domain-containing-protein
MDGIDWPEVCNWFNSFRFVFTVLIATWIFTRGSAPKRGRYGLRVALVVAAGIILAVSNPLYVGTDNPLPWLSVSNFVRVWIAVTFLLALLSIKFLRRTSWTNALSRWAMGLCVERFITSFIHNWLFLIIIKDFKTERPLSYIAISLFIYGLFLMMSAHWLAPLFARDLTPLKNDGGKESRTLCMLYILGVVALYLVTNASMGISEQYVDLLRKLIGGDAEGRTLLDYILYFSTGMAGLVALLIFLFQYAIYHTTELRHESALLQVLSEQKSRQFDTISANIDYINHKSHDLKHQIDALEYAEGSRRGALVREVRNALNLYDSTANTGNDALDTLITERNFFCARNGIRMTCSLAGCDWDAIDVVDLYTILGNALDNACDYVMRFDNPDKRVISVSARQKGNLIVLSIDNYFEETLDMADGLPKTTKPDTFSHGLGLKSIRNIAHRYGGDILVTAKPPIFTLQISLFTDVVRERTDKPKVS
>NZ_CP026729.1|WP_154304321.1|2337238_2340145_+|beta-glucosidase
MSRKGKARRPLPYIASAAIILIVILVSVATIIGNVYASKYSDLISVYFNQKTSKVVSADNETTEHFKSDYASDKERQKALGKMGTDILREGVTLLKNNDSALPLSKNAKISVFGQDSVDPVYGGGGAGSIDTSKAKSLLSAFKDAGFDVNPTLTDFYTKGAGKDYRKTSTDAYGKGEFAVNEVPVSKYTDDVKKSFSEYDDAAVVIIGRSGSESQDLPTGKLASGYTYLQLDDNERAMLKMASGNFDKVVVLLNTQNPMELKDLEDDSVDAVLWIGSLGQTGATGVAEALNGTVNPSGHLTDTYAYDLKSAPSSANFGSYTIVNSSQPFSTSYMAYSEGIYVGYRYYETRYEDVVLGNEDKANYDYAEQVEYPFGYGLSYTDFEWSNYAMKKTADGYDMSVKVTNTGKTDGKDVVQLYMQSPYTDYDRRNGIEKVSNELVGFAKTKLLKTGESETVTIHVDKESLKTYDAKGEGTYIVDAGDYYFAVGTDAHDALNNILAVKGKTTSDGMTSRGDASLASKDTIRTQDDKTYAESAETGKKISNQFQDVDLATYDGSFKYLSRSDWNGTWLATYKDGKWTAPQEFVDALAVDTKQTEPEQVPTTGKEDSSFGKLNASMLMDTDYDDETWAALIQQMSVKELDELVRIGGYATKSVNSTQLPATTDKDGPAGISSTLVGGESGMGYPGELVIASTWNTDLAEAFGKAIGEDSIALKVAVWYGPACNIHRNPYGGRAFEYFSEDSFLSGAMCAKVVSGARSKGVVPTVKHFALNDQETNRMGGAILANEQTVRQLYLKPFEMSVRDGGATAMMASMNRIGTRWTGGHKGLLTNTLRGEWGFNGFVVTDQASYSVFAYEDMREGLEAGTDLWLNTDASLWKLDKADMTDGVISNMQRAAHNISYAISHSNAMNGLSANSKIVNVTPLWRWGVYALDALVAIGSVATIVFSVMQIIRRRQMATATVTVESSQ
>NZ_CP026729.1|WP_154304323.1|2347404_2350401_-|HAD-IC-family-P-type-ATPase
MVDRKEDQSTQFRDTSSGNFEQAKNIATQTQVDPSLADAQTVAQSLGVDLNTGLSQAEAKRRLDKYGPNELASAPPVPKWKKFLEQFKDPLVYLLLAATGISLAAWFIERANAVPGAEGGEALPFDAIVIVLILIVNAVLGYIQESKAEAAVEALSSMTAPQTNVLRDGQIERINTVGVVPGDIIVLGEGDSVSADGRLFTAASLRIAEASLTGESVPVGKKTDTLAQAKALGDRANMVFNGTSVTQGTGRAIVTSTGMGTQVGKIADLLQATEDDETPLQKEMNYVSKILGIAVCIIAVVVLVALALTEGFQDVHDVIDSLLLAVSLAVAAVPEGLAAILTVVLALGVQRMAMHNAIVKKLHSVETLGSASVICSDKTGTLTRNEMTVERVVTPSGEVQLTGTGYAPEGRMVVDSQTMEYAQIREIIESEAVATLAVGALANDGELREVAASAGNAENVTWEAVGDPTEVSLIVAARKVKANRKYANYERVGEIPFTSERKRMSIVAQDNTDAGRLTVFSKGAPDVLLGYCSRIAVGGAVRPLTEGDRQQILATVEQLSSDAYRTLGQAYRPLGTASLAQVPGIMLNSAGHVADIAEQSDVLENDLIWVGMVGIIDPPRTEVRDSVAEAHRAGIRTVMITGDHPLTAARIATDLGIIDKDGKAMTGSQLDELPDEAAFDKVTSEVSVYARVAPEHKLKIVESLQRQGNIVAMTGDGVNDAPAVKTADIGVAMGITGTEVTKQSAKMILADDNFSTIVAAVREGRGIFNNIRKFLRYLLSSNVGEVFTVFGGVMLAGFLGITQPGSQGVIVPLLATQLLWINLLTDAAPALAMGVDPSTDDVMARKPRKLTDRVIDAEMWGDIIFIGVIMAAVTLIGMDMHLAGGLFTDRSVDAIGHDAQMTEARTMGFTILVFAQMLNAIASRSHLQSAFVGLFSNKWLWGALALSTVLQLAVIYIPFLNTAFGTVPLSAGAWVECLGLAMIVLIASELRKCVLRAR
>NZ_CP026729.1|WP_048349547.1|2350743_2351997_-|hypothetical-protein
MCNDVSVIASSDASNASRVLNLPEGGSVRLCGAMDVQRVTIGERTGLRPIRLPLSGLVQRSLYEYETVRTVVSGCSGVHLRVRTAADAIRLAVRAARVDYGELNSEFNAFAATVDGRTVCEVTSQPDAIERVSRDGRTCVRTELDECSVVEFTGLGAIGEKTVVIWLPQTVIVDLLGVSGVHGEPVEAAEESSTPRWLHYGSSISHCHTPSSPLQVWPVLAAGLNDLEVTNLGFAGQCMLDPYVAKAIAASDADVITLSVGVNITGARAMNQRTFTPALHGFLDVIRERHPDTPIVLVSSIYWPDSDDVPGPSDVRFHDDGSVTCYSYGDRKEIAVGALTLEQSREELQHVTQVRHDTYGENIQYLDGLTLFGPSDVGNFCLPDGLHPDAQLYAEIARRFSCQVFADNGLVPRASLH
>NZ_CP026729.1|WP_033501964.1|2352018_2352828_-|alpha/beta-hydrolase
MNLKPISFDVEGLTLRGSVYEPKGGFEQEKRYPTALLFHGFGGNRIDFSGFMMQMARSLSQQGIVAITYDRAGHGESDGTFFDVSISREVRHAKQVLQQVCSLDYVDENNLHFGGISLGAVVESIVASETAAKPRSMVMVSSAASCVDEITSGKIQGKSLEGLRTQSYFDFMGAKMGPAMVEDVKGLDLYAKVTGCTSDVLLIHGTADFVPVEYAQRYKDVFGDRATLIVKENGDHGFCSVPDREFVMSKTAQFIAEHAGVSYQGVEIF
>NZ_CP026729.1|WP_128832457.1|2352824_2354042_-|MFS-transporter
MATFVDNAATMGVSTAFVLYQSGGRLTGNQIGMLTSSVTIGVALGSFLGGRLGDRFGRRHVFVGTMLIIILGAFIPFISTDFAFMLPGVLLLGLGIGADLPVAMATISETATDKNRAKILVFSNLLGGFGILMSVLLGIFFGNSGVFGGHVIFGAFGGVAVIVLLMRLTIPETETWLKANEERKEGVHTLRADNSSVKDLMKTPWRKPFVTLVCYYSLVAISVSVSSGFGTYIAYNVANISVSTYSTASLACMPLAILGAAWFMAVADSKWRMTYYVIGSVLVAVSGLIPVIFGFNLVTLCAFTYIVTFAGAFCYETIMKVWTQESFPTMLRGTAQGFIYGISRVLTAIMSAVTPALLVFNPKMLYVSIALLSAVGFFVGWLGFHKSTGNTFQTEAQVESEGALQ

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

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

859176 : 899359

Bifidobacterium_phage(42.86%)

tRNA,integrase,coat,portal,tail,terminase

attL 862147:862161|attR 904490:904504

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_154303683.1\|859176_859776_+\|tRNA	aminoacyl-tRNA hydrolase	NA	NA	NA	NA
WP_154303684.1\|859765_863314_+	transcription-repair coupling factor	NA	NA	NA	NA
862147:862161	attL	NA	NA	NA	NA
WP_003835282.1\|863451_864750_+	phosphopyruvate hydratase	W6LP63	Streptococcus_phage	2.0e-131	55.8
WP_154303685.1\|864828_865386_+	septum formation initiator family protein	NA	NA	NA	NA
WP_154303686.1\|865394_865961_+	DUF501 domain-containing protein	NA	NA	NA	NA
WP_154303687.1\|865988_866984_+	Ppx/GppA family phosphatase	NA	NA	NA	NA
WP_154304382.1\|867245_867734_-	hypothetical protein	NA	NA	NA	NA
WP_154303688.1\|868031_868634_-	hypothetical protein	NA	NA	NA	NA
WP_154304383.1\|868678_869059_-	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_154303689.1\|869078_869441_-	XRE family transcriptional regulator	NA	NA	NA	NA
WP_154303690.1\|869558_869687_+	anhydro-N-acetylmuramyl-tripeptide amidase	NA	NA	NA	NA
WP_154303691.1\|869674_869923_+	hypothetical protein	NA	NA	NA	NA
WP_154303692.1\|869934_870153_+	hypothetical protein	NA	NA	NA	NA
WP_154303693.1\|870149_870332_+	hypothetical protein	NA	NA	NA	NA
WP_154303694.1\|870328_870553_+	hypothetical protein	I3NLC5	Bifidobacterium_phage	3.7e-14	54.1
WP_154303695.1\|870995_871298_+	hypothetical protein	NA	NA	NA	NA
WP_154303696.1\|871294_871513_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_154303697.1\|871509_871689_+	hypothetical protein	NA	NA	NA	NA
WP_154303698.1\|871685_872324_+	molecular chaperone GrpE	NA	NA	NA	NA
WP_154303699.1\|872475_873447_+	endonuclease	D2IYT8	Enterococcus_phage	2.0e-24	30.8
WP_154303700.1\|873449_874286_+	DNA-binding protein	A0A1P8DTF2	Proteus_phage	2.3e-48	46.4
WP_154303701.1\|874285_874765_+	single-stranded DNA-binding protein	A6N1Y1	Microbacterium_phage	4.2e-39	60.0
WP_154304384.1\|874889_875276_+	hypothetical protein	NA	NA	NA	NA
WP_154303702.1\|875278_875812_+	hypothetical protein	NA	NA	NA	NA
WP_154303703.1\|875808_876123_+	hypothetical protein	NA	NA	NA	NA
WP_154303704.1\|876119_876431_+	hypothetical protein	NA	NA	NA	NA
WP_162008471.1\|876452_876599_+	hypothetical protein	NA	NA	NA	NA
WP_154303706.1\|876595_876910_+	hypothetical protein	NA	NA	NA	NA
WP_154303707.1\|877184_877982_+	hypothetical protein	A0A1U9WS24	Gordonia_phage	4.2e-07	31.3
WP_154303708.1\|877978_878137_+	GTP-binding protein	NA	NA	NA	NA
WP_154303709.1\|878234_878618_+	DUF3310 domain-containing protein	A0A2H4P9W5	Gordonia_phage	3.0e-11	57.9
WP_154303710.1\|878614_878839_+	hypothetical protein	NA	NA	NA	NA
WP_154303711.1\|878835_878979_+	antitoxin	NA	NA	NA	NA
WP_154303712.1\|878975_879731_+	PhnA protein	I3NLB4	Bifidobacterium_phage	3.3e-14	27.1
WP_154303714.1\|880734_881286_+	hypothetical protein	NA	NA	NA	NA
WP_154303715.1\|881287_882406_+\|terminase	terminase	A0A1C9EHW4	Gordonia_phage	2.2e-110	55.1
WP_154303716.1\|882392_883046_+\|terminase	terminase	A0A1C9EHV3	Gordonia_phage	1.6e-57	52.4
WP_154303717.1\|883048_884569_+\|portal	phage portal protein	D7NW49	Streptomyces_phage	5.6e-69	33.8
WP_154303718.1\|884450_885668_+	hypothetical protein	A0A1C9EHV4	Gordonia_phage	2.6e-32	35.4
WP_154303719.1\|885679_886270_+	hypothetical protein	NA	NA	NA	NA
WP_154303720.1\|886281_887223_+\|coat	coat protein	D7NW53	Streptomyces_phage	1.5e-48	39.7
WP_154303721.1\|887248_887830_+	hypothetical protein	NA	NA	NA	NA
WP_154303722.1\|887826_888240_+	hypothetical protein	I3NL96	Bifidobacterium_phage	2.3e-25	67.1
WP_154303723.1\|888236_888614_+	hypothetical protein	I3NL95	Bifidobacterium_phage	7.9e-17	44.2
WP_154303724.1\|888614_889031_+	transcriptional regulator	I3NL94	Bifidobacterium_phage	1.1e-22	44.9
WP_144090520.1\|889052_889571_+	hypothetical protein	I3NL93	Bifidobacterium_phage	5.8e-42	51.5
WP_154303725.1\|889674_890184_+	hypothetical protein	I3NL92	Bifidobacterium_phage	1.3e-17	39.9
WP_154303726.1\|890234_890507_+	hypothetical protein	I3NL91	Bifidobacterium_phage	5.7e-09	45.2
WP_154303727.1\|890522_893924_+\|tail	phage tail tape measure protein	I3NL90	Bifidobacterium_phage	4.1e-136	48.5
WP_154303728.1\|893910_894765_+	hypothetical protein	NA	NA	NA	NA
WP_154303729.1\|894731_896288_+	hypothetical protein	NA	NA	NA	NA
WP_154303730.1\|896287_896539_+	hypothetical protein	NA	NA	NA	NA
WP_154303731.1\|896535_897363_+	hypothetical protein	NA	NA	NA	NA
WP_154303732.1\|897490_897715_-	hypothetical protein	NA	NA	NA	NA
WP_162008472.1\|897850_898150_-	hypothetical protein	NA	NA	NA	NA
WP_154303733.1\|898186_898432_-	hypothetical protein	NA	NA	NA	NA
WP_154303734.1\|898486_899359_-\|integrase	tyrosine-type recombinase/integrase	A0A286S1S8	Klebsiella_phage	7.8e-07	27.9
904490:904504	attR	NA	NA	NA	NA

DBSCAN-SWA_2

906369 : 947941

Bifidobacterium_phage(40.91%)

integrase,holin,head,transposase,portal,tail

attL 923099:923113|attR 945440:945454

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_131205763.1\|906369_907224_+\|transposase	IS3 family transposase	A0A1B1P773	Bacillus_phage	3.0e-48	39.5
WP_154303742.1\|907220_907406_-	hypothetical protein	NA	NA	NA	NA
WP_154303743.1\|907704_908259_+	hypothetical protein	NA	NA	NA	NA
WP_154303744.1\|908320_908527_-	hypothetical protein	I3NLD9	Bifidobacterium_phage	3.9e-26	83.8
WP_154303745.1\|910906_911521_-	hypothetical protein	NA	NA	NA	NA
WP_154304385.1\|911566_911944_-	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_144171196.1\|911963_912341_-	XRE family transcriptional regulator	NA	NA	NA	NA
WP_081028318.1\|912455_912704_+	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_154303746.1\|912728_912953_+	hypothetical protein	NA	NA	NA	NA
WP_154303747.1\|912949_913165_+	hypothetical protein	NA	NA	NA	NA
WP_154303748.1\|913161_913374_+	hypothetical protein	NA	NA	NA	NA
WP_154303749.1\|913822_914128_+	hypothetical protein	NA	NA	NA	NA
WP_154303750.1\|914124_914343_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_154303751.1\|914339_914519_+	hypothetical protein	NA	NA	NA	NA
WP_154303752.1\|914515_915160_+	molecular chaperone GrpE	NA	NA	NA	NA
WP_154303753.1\|915311_916283_+	endonuclease	I4AZN3	Saccharomonospora_phage	3.2e-25	28.9
WP_154303754.1\|916285_917122_+	DNA-binding protein	Q858E1	Salmonella_phage	1.8e-48	48.3
WP_154303755.1\|917121_917604_+	single-stranded DNA-binding protein	A6N1Y1	Microbacterium_phage	2.7e-41	71.4
WP_154304386.1\|917725_918112_+	hypothetical protein	NA	NA	NA	NA
WP_154303757.1\|918114_918411_+	hypothetical protein	NA	NA	NA	NA
WP_154303758.1\|918407_918719_+	hypothetical protein	NA	NA	NA	NA
WP_154303759.1\|918715_919195_+	hypothetical protein	NA	NA	NA	NA
WP_154303760.1\|919191_919509_+	hypothetical protein	NA	NA	NA	NA
WP_154303761.1\|919678_920470_+	hypothetical protein	NA	NA	NA	NA
WP_154303708.1\|920466_920625_+	GTP-binding protein	NA	NA	NA	NA
WP_154303709.1\|920722_921106_+	DUF3310 domain-containing protein	A0A2H4P9W5	Gordonia_phage	3.0e-11	57.9
WP_154303710.1\|921102_921327_+	hypothetical protein	NA	NA	NA	NA
WP_154303711.1\|921323_921467_+	antitoxin	NA	NA	NA	NA
WP_154303762.1\|921463_922219_+	PhnA protein	I3NLB4	Bifidobacterium_phage	9.7e-14	27.5
923099:923113	attL	NA	NA	NA	NA
WP_051662174.1\|923149_923713_+	hypothetical protein	A0A1C9EHY3	Gordonia_phage	2.2e-18	40.8
WP_034880959.1\|923709_925335_+	hypothetical protein	D7NW48	Streptomyces_phage	6.2e-143	47.5
WP_051662175.1\|925345_926800_+\|portal	phage portal protein	A0A0K2CMY3	Mycobacterium_phage	5.5e-66	35.9
WP_034881132.1\|926837_927701_+	hypothetical protein	A0A1C9EHV4	Gordonia_phage	4.8e-17	28.8
WP_051662176.1\|927788_928331_+	hypothetical protein	NA	NA	NA	NA
WP_034880961.1\|928358_929336_+	hypothetical protein	G9FH86	Rhodococcus_phage	1.5e-115	62.4
WP_152548811.1\|929338_929551_+	hypothetical protein	NA	NA	NA	NA
WP_034880964.1\|929547_929769_+\|head	head protein	NA	NA	NA	NA
WP_034880966.1\|929773_930196_+	hypothetical protein	NA	NA	NA	NA
WP_080704331.1\|930206_930629_+	hypothetical protein	I3NL96	Bifidobacterium_phage	1.4e-25	68.3
WP_034880968.1\|930625_931003_+	hypothetical protein	I3NL95	Bifidobacterium_phage	1.1e-15	42.6
WP_034880970.1\|931003_931420_+	hypothetical protein	I3NL94	Bifidobacterium_phage	8.2e-23	44.9
WP_154303763.1\|931444_931963_+	hypothetical protein	I3NL93	Bifidobacterium_phage	1.3e-41	50.9
WP_154303764.1\|932064_932574_+	hypothetical protein	I3NL92	Bifidobacterium_phage	2.2e-17	38.0
WP_154303765.1\|932912_936377_+\|tail	phage tail tape measure protein	I3NL90	Bifidobacterium_phage	4.6e-135	45.9
WP_154303766.1\|936363_937218_+	hypothetical protein	NA	NA	NA	NA
WP_154303729.1\|937184_938741_+	hypothetical protein	NA	NA	NA	NA
WP_154303730.1\|938740_938992_+	hypothetical protein	NA	NA	NA	NA
WP_154303767.1\|938988_939771_+	hypothetical protein	NA	NA	NA	NA
WP_162008472.1\|939807_940107_+	hypothetical protein	NA	NA	NA	NA
WP_154303768.1\|940254_940449_+	hypothetical protein	NA	NA	NA	NA
WP_154303732.1\|940576_940801_-	hypothetical protein	NA	NA	NA	NA
WP_154303734.1\|940939_941812_-\|integrase	tyrosine-type recombinase/integrase	A0A286S1S8	Klebsiella_phage	7.8e-07	27.9
WP_154303735.1\|941924_942323_+	hypothetical protein	NA	NA	NA	NA
WP_154303769.1\|942340_943918_+	hypothetical protein	NA	NA	NA	NA
WP_154303770.1\|944285_945377_+	reverse transcriptase	A0A0C5K882	ANMV-1_virus	2.2e-19	27.7
WP_154303771.1\|945943_946255_+	hypothetical protein	I3NL84	Bifidobacterium_phage	5.6e-08	51.6
945440:945454	attR	NA	NA	NA	NA
WP_162008473.1\|946400_947639_+	LysM peptidoglycan-binding domain-containing protein	Q8LTJ6	Lactococcus_phage	2.9e-31	38.3
WP_154303773.1\|947650_947941_+\|holin	holin	NA	NA	NA	NA

DBSCAN-SWA_3

1235804 : 1243056

Streptococcus_phage(85.71%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_000228166.1\|1235804_1236674_+	hypothetical protein	A0A1X9I6C9	Streptococcus_phage	4.3e-159	95.8
WP_000662263.1\|1236654_1237389_+	class I SAM-dependent methyltransferase	A0A1X9I6N4	Streptococcus_phage	1.5e-141	100.0
WP_001255864.1\|1237421_1238330_+	aminoglycoside nucleotidyltransferase ANT(6)-Ia	E4ZFP8	Streptococcus_phage	2.0e-167	93.4
WP_000627290.1\|1238326_1238869_+	streptothricin N-acetyltransferase Sat4	A0A1B0RXL7	Streptococcus_phage	8.9e-94	100.0
WP_001096887.1\|1238961_1239756_+	aminoglycoside O-phosphotransferase APH(3')-IIIa	E4ZFP6	Streptococcus_phage	2.3e-154	100.0
WP_001079938.1\|1240031_1240604_+	HTH domain-containing protein	A0A1B0RXM1	Streptococcus_phage	5.5e-102	99.5
WP_070097856.1\|1241554_1241905_+	hypothetical protein	NA	NA	NA	NA
WP_048349578.1\|1241901_1243056_-	DNA methylase	A0A2P1N159	Mycobacterium_phage	5.1e-99	49.9

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_CP026729

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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