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_CP011020	Pseudomonas chlororaphis strain UFB2 chromosome, complete genome	3 crisprs	csa3,DEDDh,PD-DExK,cas3,DinG,WYL,RT	0	0	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP011020_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP011020_1

141371-141447

Orphan

Consensus_repeat	Method
GCAAGCCCGCTCCCACAAGGGATT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP011020_1

>merge|NZ_CP011020|1|141371-141447|CRISPRCasFinder
GCAAGCCCGCTCCCACAAGGGATTTGGGGTGTACGAAGCCTTTGCATGCACCAGCAAGCCCGCTCCCACAGGGGATT

>NZ_CP011020|1|1|141371-141447|CRISPRCasFinder
GCAAGCCCGCTCCCACAAGGGATT	TGGGGTGTACGAAGCCTTTGCATGCACCA
GCAAGCCCGCTCCCACAGGGGATT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011020.1\|WP_042728651.1\|133162_134014_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|226644
NZ_CP011020.1\|WP_042728656.1\|139824_140736_-\|dihydrodipicolinate-synthase-family-protein	unknown	unknown	gnl\|CDD\|188630
NZ_CP011020.1\|WP_047735493.1\|132151_133150_-\|4-hydroxyproline-epimerase	unknown	unknown	gnl\|CDD\|184428
NZ_CP011020.1\|WP_042729723.1\|147415_149035_+\|inorganic-phosphate-transporter	unknown	unknown	gnl\|CDD\|223383
NZ_CP011020.1\|WP_047735498.1\|145240_146176_-\|phosphatase	unknown	unknown	gnl\|CDD\|274735
NZ_CP011020.1\|WP_047735496.1\|138314_139832_-\|aldehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143430
NZ_CP011020.1\|WP_042728657.1\|141483_142437_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|188320
NZ_CP011020.1\|WP_042728652.1\|134010_134859_-\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|226644
NZ_CP011020.1\|WP_042728653.1\|136051_136900_-\|glycine-betaine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270357
NZ_CP011020.1\|WP_042728661.1\|142656_143901_-\|saccharopine-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|224662
NZ_CP011020.1\|WP_047735500.1\|149268_150012_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP011020.1\|WP_047735495.1\|136971_138318_-\|FAD-binding-oxidoreductase	unknown	unknown	gnl\|CDD\|223737
NZ_CP011020.1\|WP_047735502.1\|150676_152899_-\|TonB-dependent-siderophore-receptor	unknown	unknown	gnl\|CDD\|273805
NZ_CP011020.1\|WP_042728648.1\|129793_131425_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP011020.1\|WP_042728662.1\|143926_145024_-\|carboxynorspermidine-decarboxylase	unknown	unknown	gnl\|CDD\|143502
NZ_CP011020.1\|WP_047735499.1\|146431_147346_+\|polyphosphate-kinase-2	unknown	unknown	gnl\|CDD\|213852
NZ_CP011020.1\|WP_042729721.1\|150079_150463_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_042728660.1\|134855_135974_-\|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226643
NZ_CP011020.1\|WP_047735492.1\|131671_132100_+\|DUF1810-domain-containing-protein	unknown	unknown	gnl\|CDD\|378062
NZ_CP011020.1\|WP_042729719.1\|153021_153423_-\|ParB-N-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|319257

Protein	Function_ID	Function_description	E-value
NZ_CP011020.1\|WP_042728651.1\|133162_134014_-\|ABC-transporter-permease-subunit	gnl\|CDD\|226644	COG4176, ProW, ABC-type proline/glycine betaine transport system, permease component [Amino acid transport and metabolism].	1.14474e-106
NZ_CP011020.1\|WP_042728656.1\|139824_140736_-\|dihydrodipicolinate-synthase-family-protein	gnl\|CDD\|188630	cd00408, DHDPS-like, Dihydrodipicolinate synthase family. Dihydrodipicolinate synthase family. A member of the class I aldolases, which use an active-site lysine which stabilizes a reaction intermediate via Schiff base formation, and have TIM beta/alpha barrel fold. The dihydrodipicolinate synthase family comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways and includes such proteins as N-acetylneuraminate lyase, MosA protein, 5-keto-4-deoxy-glucarate dehydratase, trans-o-hydroxybenzylidenepyruvate hydratase-aldolase, trans-2'-carboxybenzalpyruvate hydratase-aldolase, and 2-keto-3-deoxy- gluconate aldolase. The family is also referred to as the N-acetylneuraminate lyase (NAL) family.	1.01137e-93
NZ_CP011020.1\|WP_047735493.1\|132151_133150_-\|4-hydroxyproline-epimerase	gnl\|CDD\|184428	PRK13971, PRK13971, 4-hydroxyproline epimerase.	0
NZ_CP011020.1\|WP_042729723.1\|147415_149035_+\|inorganic-phosphate-transporter	gnl\|CDD\|223383	COG0306, PitA, Phosphate/sulphate permeases [Inorganic ion transport and metabolism].	3.78009e-57
NZ_CP011020.1\|WP_047735498.1\|145240_146176_-\|phosphatase	gnl\|CDD\|274735	TIGR03706, exo_poly_only, exopolyphosphatase. It appears that a single enzyme may act as both exopolyphosphatase (Ppx) and guanosine pentaphosphate phosphohydrolase (GppA) in a number of species. Members of the seed alignment use to define this exception-level model are encoded adjacent to a polyphosphate kinase 1 gene, and the trusted cutoff is set high enough (425) that no genome has a second hit. Therefore all members may be presumed to at least share exopolyphospatase activity, and may lack GppA activity. GppA acts in the stringent response. [Central intermediary metabolism, Phosphorus compounds].	5.79016e-86
NZ_CP011020.1\|WP_047735496.1\|138314_139832_-\|aldehyde-dehydrogenase	gnl\|CDD\|143430	cd07112, ALDH_GABALDH-PuuC, Escherichia coli NADP+-dependent gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase PuuC-like. NADP+-dependent, gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (GABALDH) PuuC of Escherichia coli which catalyzes the conversion of putrescine to 4-aminobutanoate and other similar sequences are present in this CD.	0
NZ_CP011020.1\|WP_042728657.1\|141483_142437_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|188320	TIGR03418, chol_sulf_TF, putative choline sulfate-utilization transcription factor. Members of this protein family are transcription factors of the LysR family. Their genes typically are divergently transcribed from choline-sulfatase genes. That enzyme makes choline, a precursor to the osmoprotectant glycine-betaine, available by hydrolysis of choline sulfate.	5.86189e-57
NZ_CP011020.1\|WP_042728652.1\|134010_134859_-\|ABC-transporter-permease-subunit	gnl\|CDD\|226644	COG4176, ProW, ABC-type proline/glycine betaine transport system, permease component [Amino acid transport and metabolism].	2.98497e-98
NZ_CP011020.1\|WP_042728653.1\|136051_136900_-\|glycine-betaine-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270357	cd13639, PBP2_OpuAC_like, Substrate binding domain of Lactococcus lactis ABC-type transporter OpuA and related proteins; the type 2 periplasmic binding protein fold. This subfamily is part of a high affinity multicomponent binding-protein-dependent transport system specific to betaine compounds for osmoregulation. The periplasmic substrate-binding domain, which is often fused to the permease component of the ATP-binding cassette transporter complex, is involved in uptake of osmoprotectants (also termed compatible solutes) such as glycine betaine and proline betaine. Many microorganisms accumulate these compatible solutes in response to high osmolarity to offset the loss of cell water. This domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.22852e-100
NZ_CP011020.1\|WP_042728661.1\|142656_143901_-\|saccharopine-dehydrogenase-family-protein	gnl\|CDD\|224662	COG1748, LYS9, Saccharopine dehydrogenase and related proteins [Amino acid transport and metabolism].	1.5253e-145
NZ_CP011020.1\|WP_047735500.1\|149268_150012_+\|SDR-family-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	3.03398e-48
NZ_CP011020.1\|WP_047735495.1\|136971_138318_-\|FAD-binding-oxidoreductase	gnl\|CDD\|223737	COG0665, DadA, Glycine/D-amino acid oxidases (deaminating) [Amino acid transport and metabolism].	4.88473e-42
NZ_CP011020.1\|WP_047735502.1\|150676_152899_-\|TonB-dependent-siderophore-receptor	gnl\|CDD\|273805	TIGR01783, Ferrienterobactin_receptor, TonB-dependent siderophore receptor. This subfamily model encompasses a wide variety of TonB-dependent outer membrane siderophore receptors. It has no overlap with TonB receptors known to transport other substances, but is likely incomplete due to lack of characterizations. It is likely that genuine siderophore receptors will be identified which score below the noise cutoff to this model at which point the model should be updated. [Transport and binding proteins, Cations and iron carrying compounds, Transport and binding proteins, Porins].	1.33987e-103
NZ_CP011020.1\|WP_042728648.1\|129793_131425_+\|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.	1.49846e-49
NZ_CP011020.1\|WP_042728662.1\|143926_145024_-\|carboxynorspermidine-decarboxylase	gnl\|CDD\|143502	cd06829, PLPDE_III_CANSDC, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Carboxynorspermidine Decarboxylase. Carboxynorspermidine decarboxylase (CANSDC) catalyzes the decarboxylation of carboxynorspermidine, the last step in the biosynthesis of norspermidine. It is homologous to eukaryotic ornithine decarboxylase (ODC) and diaminopimelate decarboxylase (DapDC), which are fold type III PLP-dependent enzymes that contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. Based on this similarity, CANSDC may require homodimer formation and the presence of the PLP cofactor for its catalytic activity.	0
NZ_CP011020.1\|WP_047735499.1\|146431_147346_+\|polyphosphate-kinase-2	gnl\|CDD\|213852	TIGR03707, PPK2_P_aer, polyphosphate kinase 2, PA0141 family. Members of this protein family are designated polyphosphate kinase 2 (PPK2) after the characterized protein in Pseudomonas aeruginosa. This family comprises one of three well-separated clades in the larger family described by pfam03976. PA0141 from this family has been shown capable of operating in reverse, with GDP preferred (over ADP) as a substrate, producing GTP (or ATP) by transfer of a phosphate residue from polyphosphate. Most species with a member of this family also encode a polyphosphate kinase 1 (PPK1). [Central intermediary metabolism, Phosphorus compounds].	1.02884e-153
NZ_CP011020.1\|WP_042728660.1\|134855_135974_-\|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	gnl\|CDD\|226643	COG4175, ProV, ABC-type proline/glycine betaine transport system, ATPase component [Amino acid transport and metabolism].	1.46823e-166
NZ_CP011020.1\|WP_047735492.1\|131671_132100_+\|DUF1810-domain-containing-protein	gnl\|CDD\|378062	pfam08837, DUF1810, Protein of unknown function (DUF1810). This is a family of uncharacterized proteins. The structure of one of the members in this family has been solved and it adopts a mainly alpha helical structure.	3.82068e-62
NZ_CP011020.1\|WP_042729719.1\|153021_153423_-\|ParB-N-terminal-domain-containing-protein	gnl\|CDD\|319257	cd16400, ParB_Srx_like_nuclease, ParB/Srx_like nuclease and putative transcriptional regulators related to SbnI. This family contains a Pyrococcus Furiosus enzyme reported to have DNA nuclease activity and resembles the N-terminal domain of ParB proteins of the parABS bacterial chromosome partitioning system. This sub-family also includes siderophore staphylobactin biosynthesis protein SbnI. 60% of the P. furiosus nuclease activity was retained at 90 degree C, suggesting a physiological role in the organism, which can grow in temperatures as high as 100 degrees Celsius. The protein has endo- and exo-nuclease activity vs. single- and double-stranded DNA, and nuclease activity was lost in methylated proteins prepared for structure solution. This family has a fairly well-conserved DGHHR motif that corresponds to the same structural position as the phosphorylation site (a portion of the ATP-Mg-binding site) of sulfiredoxin and the arginine-rich ParB BoxII of ParB.	2.24881e-28

>NZ_CP011020.1|WP_042728656.1|139824_140736_-|dihydrodipicolinate-synthase-family-protein
MRFEGIYTPAVTPHTPDGDIDWNVFDDVLESLVEAKVHGIIIGGSTGEYYAQTAEERLELAARAKDVIGSRVQLIIGTGAIRTEDAVLFAKDAKAIKADAILVTTPPYALPTDQENAIHALTIDRAANLPIMLYNYPGRMCVQMNEDYLARVGKSKNVVAIKESSGDMGRVHLLAREFPHIALSCGWDDQALEFFAWGARSWVCAGSNFLPREHVALYEACVLEKNFDKGRQIMSAMMPLMNALDGGKFVQSIKFGCELNGLKVGDVRAPLRPLNAGDKRSLQTVIANVKRTVAHITSGANHA
>NZ_CP011020.1|WP_047735496.1|138314_139832_-|aldehyde-dehydrogenase
MRDLLTAAEYAAIAKSISFPSNAFIDGAFKPAIGGKTFATHNPATGAFLADIAACTVEDVDYAVSKAREAFEDGRWRLLAPGERKAVLLKFAKLLEDNRHELAVLESLDSGKPVRECQCVDVPDTIHTLRWHAEVIDKLYDHTAPVGNDALTMVVREPIGVVGCVLPWNFPLLMLAWKIGPALAAGCSVIVKPAEQTTLTTLRVAELAFEAGVPAGVLNIVTGTGKDVGEPIGLHKDVDMVSFTGSTATGRRFLHYAADSNLKRVVLECGGKNPAVVMDDAEDLDLVAEQVVNGAFWNMGENCSATSRLLVHASVKDELLQRMGAYLNEWKMGDPLDPHNRVGALVSSDHFEKVKSYLDYANGDKLAVVYGGDTQDGAFVQPTVIDGVDRDSRLFQEEIFGPVLSVTSFTSICEAIALANDTAYGLAASVYTGSLRKAIKLSREIRAGIVTVNCFGEGDASTPFGGYKESGFGGRDKSVFAHDQYTEIKTIWIDVSDRSVDETVK
>NZ_CP011020.1|WP_047735495.1|136971_138318_-|FAD-binding-oxidoreductase
MSAHTIKRLPVDTGVSGWEAISTRSTPVRMLDGQVTADWVIIGAGFAGLSAARRLSQLRPGERIVVLDAHEVAKGPAGRNSGFMIDVPHNLSSGEYSVAGESATALEIAQNRFAIDFASQAAHEYGMSAHTFDPSGKINAAATERGLKLNDNYAKSLHGIGERYELFDAAQMREITGSTYYHGGLYTPGAVMIQPAQYIRDLAAGLADKVTLLERSPVIELSRTGGDWVARSHRGTVTAPKVILAVNGHIEDFGHFKGRLLHVFTYASMTAGYRDEQFDKTLPGRDRWALLPADPMGATLRKITSDGLSRIVIRTKFTYDPSIQVTPKRVAAVAQEQRHSLDLRFPELKDTPFEFSWAGRLCLSRNSAPAFGEIEPNLYSACCENGLGTVKSTLAGVMAAELATGTDSKFLESFSHAPGPSRLPPRLLTQWGVRSVIRWQAFKAGKEG
>NZ_CP011020.1|WP_042728653.1|136051_136900_-|glycine-betaine-ABC-transporter-substrate-binding-protein
MNKIWKTVCAVAIAGMMSLQAHAEEKTITMGTMNWEDLTPITGITKKVLEDSGYTVKVVEFSEWGIAYAALTKGDVQVLASQTDYAASDYWNKNKNKLEKLSPVSFGLYQGLAVPSYVDIDSIDQLNANADKFGGKIIGIEPGSGLMSDATNVVKAYDLKLKLIEGSTSAMTAALKSAVDRKEWVAVTVWDPSWMTKKFDLKFLKDPKAIFPPLQGYYWIGHKGFAEANPRARELMASVYVPIADITSMNAEVKDGKTMEQAVKGWTDSHSDLLKRWGNIKN
>NZ_CP011020.1|WP_042728660.1|134855_135974_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein
MTTAKIDTHEVLVDCQSVWKIFGKSAPAAIDAVAQRGLTKTQILQEYSCVVGVSDVSLQVRRGEIFCIMGLSGSGKSTLIRLLNKLITPSAGKVLVKGKDLSALSPKALREVRARHIGMVFQSVALLPNRTVLENTAFGLEVQGVGKAERYKVAERALAKVGLSEWASRYPTELSGGMQQRVGLARAITADPEVILMDEPFSALDPLIRRQLQDEFRQLTKDLGKSAVFITHDLDEAIRIGDRIAIMKDGVIIQVGTAEEIVLNPADDYVAEFVAGISRLHLVKAHSVMTPVEPFKAANPGCDIAKLAKTTPDADIDELIGLTMKSERDALAVVDNGVVVGVITPRDLLRGVQGTANEFIAPSAVDALEAAT
>NZ_CP011020.1|WP_042728652.1|134010_134859_-|ABC-transporter-permease-subunit
MSTPDFSSQFDAAIDATLEWLSEHGEFLFDAANGALTSVYKGVLWCIAYPPSWVVALIVALVGWRMIGARFALLAGLALMFCALIGLWPETVSTLALVLTATVLALLVAIPLGVVAGLTPAFDRVVDPCLDLVQTMPPYIYLLPAIALLGYGPATALLATFIVAVPPAMRLTSLGIRMTPNEFIELGNASGVTGLQMFFKIRLPFAMPSIMAGVNQSLMMAFGMVVIAGIVGSGGLGEAIYGAVRTLDIAKSINAAIAIVILTMILDRLAQAAARTRVGDSQ
>NZ_CP011020.1|WP_042728651.1|133162_134014_-|ABC-transporter-permease-subunit
MSMSDMRFSPGQFLAPGVDWLNANLHGLFVAISQVVEAVLGFVEHALLAPHPYVLIGIVVAAAFFFANRRVALFAALMLAFCLFSGLWVASMQTIALVSVAVLISVSVAFPLGVLAARVKKVEDAFLPILNIMQTVPPWVYLIPAVMLFSLGRVPAIIATIVYGIPPMLRLTTLAFKQLPKDLLELGQASGASPRDILFKIELPTAAPTLLVGLNQCILMSLAMVVLAGLVGAGGLGAEVTRGLSRMEMGLGLRAGLAIVAVALLMDRLSRGALQRHAPAKLV
>NZ_CP011020.1|WP_047735493.1|132151_133150_-|4-hydroxyproline-epimerase
MRRSFFCIDSHACGNPVRVVAGGGPLLPAVSMAERREIFVRDHDWVRTALMFEPRGHDIMSGVIIYPSVRDDCDFGALFIEVSGCLPMCGAGTLGLSTVVIEEGLIVPRVPGTLAIETPAGRVDVAYTLEGETVDAIRLFNVASYLHSADVSVEVPGVGVLTVDIAYGGNFYAVVEPQANWAGFDGLNAADIVGLSQKLRDALADICDPVHPENSRIRGVHHIIWCDAPHNATADGRCAVFYGDKAIDRSPGGTGTSARMAQLFGKGRLKVGDTFRNESLIGTVFEGKVEAAVAVGAFAGIRPSISGWAQIIGHNTIFVDDKDPLAHGFQLA
>NZ_CP011020.1|WP_047735492.1|131671_132100_+|DUF1810-domain-containing-protein
MTESLERFVQAQTSTFETAMAELERGRKQSHWIWFIFPQLRGLGRSENAAYYGLRDIEEARDYLRHPLLGPRLERATRTVLDSSVPVQRLLGELDAMKFASCMTLFRAAAEAGSVYARALDSTVSVDVRTLEMLHKQEKNGV
>NZ_CP011020.1|WP_042728648.1|129793_131425_+|diguanylate-cyclase
MHFLPFNSLRARFAIAVASVVLVLSCLFGAAIGESSISRLKEHNGLQLSEYAYSMIDRLDRDMSSRSKSLTVLSQLQALRDPANTGEARSLLNHLSDQFPSYSWIGLTDAHGTVVASTDKLLEGADISARPVFLQGKDTTFIGDVHDAVMLAKLLPNPSGEAMKFVDISMPVRDNAGQFMGVLATHLSWKWAAEVGRSLFEPLQKRLPGLEFLVVSKDGTVLLGPKAMIGKPLGIQLDDGSGQNWSVARWQDGNLYLAGFAQSTGVDDYRGLGWTVITRQPADAAFAEAHQLRDEILIWGIVLSVVFALVGWFVAGIITGPVNQIADAAARLSQGADVRIPLLKGSREVETLSLAIRHLVDSLTRKRSQLAVAEGMAYRDTVTGLPNRAALDKYVEAVASESGERPDFGVLCLDLDGFKPVNDRFGHAMGDALLQEVGNRLLTTVRDGDIAVRHGGDEFVLLLRLRSGETLTNIQGAAQRIVAKLAEPMLLAGETLQIGCSIGGALWTGGAFSEALAQADEALYRAKRAGKSQAKFHEALELR
>NZ_CP011020.1|WP_042728657.1|141483_142437_-|LysR-family-transcriptional-regulator
MVKHIDPDLTLLKMPSLKAVKSFVAAAKYQSFTRAAEALCVTQAAISRQIRELEAYLEVDLFKRVGRAVELTEAGVIFFDAAQMSFVNISQAAERIRTHNAGKRVLTLCCSPAFSALWLSARLPTFFSQNPDIDLNLITTQNFLSMEPGIRPDIFITKMAKIQDGYQCYPLFHDVIYPVCTPQYKAAHPELSSLEGLRDGVLLNLSPYGRSQVAEHVDWGVWLAFNDIDINDRPFDSPHVLNANDYNLIITMVLTHQGVALGWNHLVEKLVEDGTLIRPVSEEVVLRESLHYLTFRQDRQNDEACCRLRDWMLAQLA
>NZ_CP011020.1|WP_042728661.1|142656_143901_-|saccharopine-dehydrogenase-family-protein
MKKNVLIIGAGGVAKVVAHKCAQHNDELGRIAIASRNISKCQAIIDSVKAKGSLKQPADIKAFALNALDVEATKALIRETESQIVINVGSAFLNMSVLRACIDTGVAYLDTAIHEEPGKVCETPPWYGNYEWKHLQECQEKNITAILGVGFDPGVVNAYAALAQQQYFDRIDSIDILDVNAGSHGKYFATNFDPEINFREFTGQVWSWQDSQWTSNTMFEVKRTDDLPVVGSQNLYLTGHDEVHSLSKNLDVPNVRFWMSFGEHYINVFTVLRNLGLLSEQPVKTAEGLEVVPLKVVKAVLPDPSSLAPGYTGKTCIGDLVKGVKDGQPREVFIYNVADHEDAFAETDSQGISYTAGVPPVAAALLVARGQWDVQRMVNVEELPAEAFLEALDVMGLPTRIKDEQGDRPWNQQA
>NZ_CP011020.1|WP_042728662.1|143926_145024_-|carboxynorspermidine-decarboxylase
MIKTPYYLIDKQKLLANMQKIAYVREQSGAKALLALKCFATWSVFDLMQQYMDGTTSSSLYELKLGRQKFAGETHAYSVAWADDEIEEMLANCDKIIFNSIGQLQRYTQASAGKVRGLRVNPQVSSSDYLLADPARPFSRLGEWDPEKIEQVIEQISGFMFHNNCENGDFGLFDQMLGTIEERFGHLLHKVEWVSLGGGIHFTGEGYALDAFCARLKAFSQKYGVQVYLEPGEAAITQSASLEVTVLDTLYNGKHLAVVDSSIEAHMLDLLIYRLNAKLAPSEGEHTYMVCGKSCLAGDIFGEYQFDRPLSIGDRLSFIDAAGYTMVKKNWFNGLKMPSIVVKQLDGSVELVREFVYDDYLSSLS
>NZ_CP011020.1|WP_047735498.1|145240_146176_-|phosphatase
MKGDAPLFAAIDLGSNAFRLMIGQTVKRNRRLVIQEVKTLREPVRLAEGLQAGALDELALDRGWQALARFGKKLRGFEAGRVRAVATSAVREAANAQLFLDSAQRHLGFRIDVLSGQEEARLVYAGVAHTVPGVEDTRLVVDIGGGSSELILGRGDQPLLTESLAIGSGTFGTRYFRDGHITAPALLEAERVASLAFEKVAMGFRAQGWQLAIGSSGTARMLAKVLKANGLNDLGQGGITYTGLLRLSLRLLEVRHVEQLRLAGLQAHRLGSLPGGLAIMLAAFKAFGITQMIASEPGLRFGVLHDLIHKR
>NZ_CP011020.1|WP_047735499.1|146431_147346_+|polyphosphate-kinase-2
MLSQDILIQRIHRELLDHTDEELELELSEDGHDMDAFFDEHTPPGSEKDSRRRYFSELFRLQGELVKLQSWVVKTGHKVVILFEGRDAAGKGGVIKRITQRLNPRVCRVAALPAPNDRERTQWYFQRYVSHLPAAGEIVLFDRSWYNRAGVEQVMGFCTADQYEEFFRTVPEFERMLARSGIQLIKYWFSISDQEQHLRFLSRLHDPLKQWKLSPMDLESRRRWEAYTKAKEIMLERTHIAEAPWWVVQADDKKKARLNCIHHLLGQMPYEEVEVPAIELPQRVRQEDYTRSPTPPELIVPQVY
>NZ_CP011020.1|WP_042729723.1|147415_149035_+|inorganic-phosphate-transporter
MTNPTLAMDSPSSVAHSSRPQLNRKPSVITLVVFFAVLGSGLLFTAYSLMHDMNELGTVVTTWTPFLLLGVALLIALGFEFVNGFHDTANAVATVIYTNSMAPNFAVAWSGFFNFLGVLLSSGAVAFGIIALLPVELILQVGSSAGFAMIFALLIAAILWNLGTWWLGLPASSSHTLIGSIIGVGVANALMHGRDGTSGVDWAQATKIGYALLLSPLVGFGCAALLLLALRAFVKNRALYKAPEGNTPPPWWIRGMLILTCTGVSFAHGSNDGQKGMGLIMLILVGTLPMAYALNRAMPADQALQFAAVAEVTQQALVKNSPLPAPADPRAILTTYVGTKEATPQLVPALAALTGSIGAEVKGYGSLARVPAEAVGNVRNDMYLTSETIRLMDKNKVGHFDADTSAKLQLFKQQIDNSTRFIPLWVKIAVAIALGLGTMVGWKRIVVTVGEKIGKSHLTYAQGASAETVAMLTIGAADMFGLPVSTTHVLSSGVAGTMVANGAGLQMRTIRNLVMAWVLTLPAAILLSGSLYWLFTRLF
>NZ_CP011020.1|WP_047735500.1|149268_150012_+|SDR-family-oxidoreductase
MHNEFKPNLSVVTGASSGIGLAVTRRLLESGSKVVAMSRQIGGLGELVERFGDLLSWLPGDVTQVADQARLAQRVGTLGQVDCLVPNAGIAQLADGLDLAAFDRQWAVNGAGALNTLSSLREHLAPEASVVFIGTFLEQATFAGLAAYIASKAALRAQMRTLAVELAPHGVRLNMVSPGPTATPIWGTLGLDEQALGSVANTVNQRLLTGQFLEPQAVADVILFQLSRGARGVYGQDWIVDNGYTLR
>NZ_CP011020.1|WP_042729721.1|150079_150463_-|hypothetical-protein
MQGNPGMTPSNARAPLRPAAEPQAHDPDRCANEPIRDLLRCYGLRTSLIRFKVINALLAAAQDGRTMGVRGVHAYLAKTSADLSFVSVREVLRRLCEEGLILFQADKTYCFTAEAWAMLEQHLDDGR
>NZ_CP011020.1|WP_047735502.1|150676_152899_-|TonB-dependent-siderophore-receptor
MSVARRPCGESALSFAIRCATLGIVLVAGSANSWAATSTSPASADANADASAPADAQGLTLDEINITGAYNGATALPPALASGQVARGARLGMMGNKDVMDTPFNVTSYTAKTLADLQTVTVADALQRDPSVRSTGQTGGIVDSFFIRGFPIGEGNIGELAYDGVYGVAPNYRVFTEYAERVEVLKGPGALMYGISPNSGIGGVINIVPKRPLDEDLTRLTTTYESDSQVGGHLDLSRRFGSENQFGVRFNGSLRGGDTVVDDQERELNIGAIALDYRGERLRLNLDFISQKESFEGASRPFTIAPGVEVPSAPNGRTNLPQKWGWSDTREQSALLGGEYDLNDSLTVFAHAGGGRSDVDRMSDQVPRILNSAGDTSNVPGHYKFNVDRSTADVGLRGVFATGPVTHTTTVMATTYQDELSRGITNGTAITSNIYHPVDAPKQYLRSPKVQRVSESELSGVAVTDTLSVLDDRLQLTLGLRRQNVESRNYSNGAVSSRYDDSATNPMVGVVVKPWDDVSFYYNYVEGLSKGDTAPSGASNSGMTFAPYESKQHELGVKYEHGTFMTTLALFQIEKPGGELGADGVFSVQAEQRNRGVELSMFGEVAPGTRLMGGVTLLDGELTESATAANRGNKPVGVPDVQANLWAEWDTPWVQGFTLTGGAIYTDKQYVNQANTQSLDAWTRFDAGARYATKIEGRPTTFRATVQNVFDREYWSGVASYGAFSAGSPRTLQLSATVDF
>NZ_CP011020.1|WP_042729719.1|153021_153423_-|ParB-N-terminal-domain-containing-protein
MQQGYQISLRPLCEVLQSEHVDPANVESVRQSIVRAGHWLEPIIVERSRGIVMDGNHRLNAALQLGLKRVPCIQLDYADPRVRVRHWQTGQAFEVARIFTTIERGELFPYKTTRHAFYPALPVIAIPLERLYG

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Crispr_ID: NZ_CP011020_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP011020_2

4479964-4480061

Orphan

Consensus_repeat	Method
CGCCTTCGCGAGCAAGCTCGCTCCCACA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP011020_2

>merge|NZ_CP011020|2|4479964-4480061|CRISPRCasFinder
CGCCTTCGCGAGCAAGCTCGCTCCCACAAGGCGCTGTGTGCTGCCGGCAGAGAGAGGGCGGCTGTCGGGCCGCCTTCGCGAGCAAGCTCGCTCCCACA

>NZ_CP011020|2|2|4479964-4480061|CRISPRCasFinder
CGCCTTCGCGAGCAAGCTCGCTCCCACA	AGGCGCTGTGTGCTGCCGGCAGAGAGAGGGCGGCTGTCGGGC
CGCCTTCGCGAGCAAGCTCGCTCCCACA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011020.1\|WP_042728243.1\|4473206_4473707_-\|PsiE-family-protein	unknown	unknown	gnl\|CDD\|225764
NZ_CP011020.1\|WP_047738264.1\|4491588_4492500_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187611
NZ_CP011020.1\|WP_042729376.1\|4483543_4484365_+\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP011020.1\|WP_042728245.1\|4471986_4472397_-\|HPF/RaiA-family-ribosome-associated-protein	unknown	unknown	gnl\|CDD\|238308
NZ_CP011020.1\|WP_042728242.1\|4474157_4474424_+\|YebG-family-protein	unknown	unknown	gnl\|CDD\|377779
NZ_CP011020.1\|WP_047738252.1\|4471030_4471909_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP011020.1\|WP_042728237.1\|4479124_4479928_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|225464
NZ_CP011020.1\|WP_047738255.1\|4480127_4480769_-\|maleylacetoacetate-isomerase	unknown	unknown	gnl\|CDD\|273527
NZ_CP011020.1\|WP_047738254.1\|4476568_4477444_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378890
NZ_CP011020.1\|WP_042728240.1\|4474775_4476407_-\|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl\|CDD\|223910
NZ_CP011020.1\|WP_047739533.1\|4484329_4485031_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_047738250.1\|4469988_4470891_-\|DMT-family-transporter	unknown	unknown	gnl\|CDD\|183067
NZ_CP011020.1\|WP_047738259.1\|4482086_4483391_-\|homogentisate-1,2-dioxygenase	unknown	unknown	gnl\|CDD\|235421
NZ_CP011020.1\|WP_042729381.1\|4492872_4493775_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP011020.1\|WP_047738258.1\|4480778_4482083_-\|fumarylacetoacetase	unknown	unknown	gnl\|CDD\|162276
NZ_CP011020.1\|WP_042728244.1\|4472892_4473210_+\|DUF3509-domain-containing-protein	unknown	unknown	gnl\|CDD\|338217
NZ_CP011020.1\|WP_047738261.1\|4485152_4487702_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225461
NZ_CP011020.1\|WP_042729378.1\|4487887_4489255_-\|DUF1329-domain-containing-protein	unknown	unknown	gnl\|CDD\|377764
NZ_CP011020.1\|WP_042729379.1\|4489277_4491071_-\|DUF1302-domain-containing-protein	unknown	unknown	gnl\|CDD\|377751
NZ_CP011020.1\|WP_042728238.1\|4477919_4478939_-\|Glu/Leu/Phe/Val-dehydrogenase	unknown	unknown	gnl\|CDD\|223411

Protein	Function_ID	Function_description	E-value
NZ_CP011020.1\|WP_042728243.1\|4473206_4473707_-\|PsiE-family-protein	gnl\|CDD\|225764	COG3223, COG3223, Predicted membrane protein [Function unknown].	3.9797e-34
NZ_CP011020.1\|WP_047738264.1\|4491588_4492500_-\|SDR-family-oxidoreductase	gnl\|CDD\|187611	cd05353, hydroxyacyl-CoA-like_DH_SDR_c-like, (3R)-hydroxyacyl-CoA dehydrogenase-like, classical(c)-like SDRs. Beta oxidation of fatty acids in eukaryotes occurs by a four-reaction cycle, that may take place in mitochondria or in peroxisomes. (3R)-hydroxyacyl-CoA dehydrogenase is part of rat peroxisomal multifunctional MFE-2, it is a member of the NAD-dependent SDRs, but contains an additional small C-terminal domain that completes the active site pocket and participates in dimerization. The atypical, additional C-terminal extension allows for more extensive dimerization contact than other SDRs. MFE-2 catalyzes the second and third reactions of the peroxisomal beta oxidation cycle. Proteins in this subgroup have a typical catalytic triad, but have a His in place of the usual upstream Asn. This subgroup also contains members identified as 17-beta-hydroxysteroid dehydrogenases, including human peroxisomal 17-beta-hydroxysteroid dehydrogenase type 4 (17beta-HSD type 4, aka MFE-2, encoded by HSD17B4 gene) which is involved in fatty acid beta-oxidation and steroid metabolism. This subgroup also includes two SDR domains of the Neurospora crassa and Saccharomyces cerevisiae multifunctional beta-oxidation protein (MFP, aka Fox2). SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	7.71693e-148
NZ_CP011020.1\|WP_042729376.1\|4483543_4484365_+\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	1.03471e-56
NZ_CP011020.1\|WP_042728245.1\|4471986_4472397_-\|HPF/RaiA-family-ribosome-associated-protein	gnl\|CDD\|238308	cd00552, RaiA, RaiA ("ribosome-associated inhibitor A", also known as Protein Y (PY), YfiA, and SpotY, is a stress-response protein that binds the ribosomal subunit interface and arrests translation by interfering with aminoacyl-tRNA binding to the ribosomal A site. RaiA is also thought to counteract miscoding at the A site thus reducing translation errors. The RaiA fold structurally resembles the double-stranded RNA-binding domain (dsRBD).	9.08163e-08
NZ_CP011020.1\|WP_042728242.1\|4474157_4474424_+\|YebG-family-protein	gnl\|CDD\|377779	pfam07130, YebG, YebG protein. This family consists of several bacterial YebG proteins of around 75 residues in length. The exact function of this protein is unknown but it is thought to be involved in the SOS response. The induction of the yebG gene occurs as cell enter into the stationary growth phase and is dependent on is dependent on cyclic AMP and H-NS.	5.14889e-25
NZ_CP011020.1\|WP_047738252.1\|4471030_4471909_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	4.32118e-28
NZ_CP011020.1\|WP_042728237.1\|4479124_4479928_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|225464	COG2912, COG2912, Uncharacterized conserved protein [Function unknown].	2.0597e-41
NZ_CP011020.1\|WP_047738255.1\|4480127_4480769_-\|maleylacetoacetate-isomerase	gnl\|CDD\|273527	TIGR01262, Maleylacetoacetate_isomerase, maleylacetoacetate isomerase. Maleylacetoacetate isomerase is an enzyme of tyrosine and phenylalanine catabolism. It requires glutathione and belongs by homology to the zeta family of glutathione S-transferases. The enzyme (EC 5.2.1.2) is described as active also on maleylpyruvate, and the example from a Ralstonia sp. catabolic plasmid is described as a maleylpyruvate isomerase involved in gentisate catabolism. [Energy metabolism, Amino acids and amines].	1.47297e-103
NZ_CP011020.1\|WP_047738254.1\|4476568_4477444_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378890	pfam12625, Arabinose_bd, Arabinose-binding domain of AraC transcription regulator, N-term. AraC is a bacterial transcriptional regulatory protein with a DNA-binding domain at the C-terminus, HTH_AraC, pfam00165, and this dimerization domain which harbours the arabinose-binding pocket at the N-terminus. AraC positively and negatively regulates expression of the proteins required for the uptake and catabolism of the sugar L-arabinose 1,2,3].	7.08648e-32
NZ_CP011020.1\|WP_042728240.1\|4474775_4476407_-\|methyl-accepting-chemotaxis-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	9.48357e-57
NZ_CP011020.1\|WP_047738250.1\|4469988_4470891_-\|DMT-family-transporter	gnl\|CDD\|183067	PRK11272, PRK11272, putative DMT superfamily transporter inner membrane protein; Provisional.	1.35954e-12
NZ_CP011020.1\|WP_047738259.1\|4482086_4483391_-\|homogentisate-1,2-dioxygenase	gnl\|CDD\|235421	PRK05341, PRK05341, homogentisate 1,2-dioxygenase; Provisional.	0
NZ_CP011020.1\|WP_042729381.1\|4492872_4493775_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.23073e-19
NZ_CP011020.1\|WP_047738258.1\|4480778_4482083_-\|fumarylacetoacetase	gnl\|CDD\|162276	TIGR01266, fum_ac_acetase, fumarylacetoacetase. This enzyme catalyzes the final step in the breakdown of tyrosine or phenylalanine to fumarate and acetoacetate. [Energy metabolism, Amino acids and amines].	0
NZ_CP011020.1\|WP_042728244.1\|4472892_4473210_+\|DUF3509-domain-containing-protein	gnl\|CDD\|338217	pfam12021, DUF3509, Protein of unknown function (DUF3509). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 92 to 110 amino acids in length. This protein has two completely conserved residues (G and R) that may be functionally important.	1.65325e-29
NZ_CP011020.1\|WP_047738261.1\|4485152_4487702_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225461	COG2909, MalT, ATP-dependent transcriptional regulator [Transcription].	7.72328e-111
NZ_CP011020.1\|WP_042729378.1\|4487887_4489255_-\|DUF1329-domain-containing-protein	gnl\|CDD\|377764	pfam07044, DUF1329, Protein of unknown function (DUF1329). This family consists of several hypothetical bacterial proteins of around 475 residues in length. The majority of family members are from Pseudomonas species but the family also contains sequences from Shewanella oneidensis and Thauera aromatica.	0
NZ_CP011020.1\|WP_042729379.1\|4489277_4491071_-\|DUF1302-domain-containing-protein	gnl\|CDD\|377751	pfam06980, DUF1302, Protein of unknown function (DUF1302). This family contains a number of hypothetical bacterial proteins of unknown function that are approximately 600 residues long. Most family members seem to be from Pseudomonas.	0
NZ_CP011020.1\|WP_042728238.1\|4477919_4478939_-\|Glu/Leu/Phe/Val-dehydrogenase	gnl\|CDD\|223411	COG0334, GdhA, Glutamate dehydrogenase/leucine dehydrogenase [Amino acid transport and metabolism].	1.02186e-82

>NZ_CP011020.1|WP_042728237.1|4479124_4479928_+|tetratricopeptide-repeat-protein
MKPRQAFFACLHRSPPALFEAALWIAAEHDRDVDVPALLRDFRDLQQRVSHDLPMLPVSELAQPLLRQLNDLGFAQDDATPLRPRAALLDKVLVGKRGQPLALGLIALELARGLEIPMVGVNFPGHFLLKVPGADHLLDPCGGRRLYPHDCRDLLHRQYGANMPLKAEHLVNAEPLQMLQRLSRNLRQLHLANDDYIAALIDAERVLELGNASAADYLARASLYQRLDCPNAERFDLEHALMLSEDPIQRLRLTERLGHLPPNSIVH
>NZ_CP011020.1|WP_042728238.1|4477919_4478939_-|Glu/Leu/Phe/Val-dehydrogenase
MFALMQSSRLESLHLSVDPMTGLKAVIAIHCSRPGPALGGCRYLAYPDDESAVADAVRLAQGMSYKAALAGLPVGGGVAVIMRPAHVESRAALFEAFGRCIEQLDGRYITAIDSGTSVADMDCIAQQTRHVTSTTASGDPAPHAAMGVFAGIRATAMARLGSDNLESLRVAIQGLGNVGYALAEQLHAAGAELLVSDIDPGKVQLAMEQLGAHPIANDALLSTPCDILAPCGLGGVLNSHSVAQLRCSAVAGSAHNQLSNLQVADQLERRGILYAPDYVINSGGLIYVALKHRGEELPSITAHLSKIGARLTEIFAHAQAEKRSPARVADELAERLLYR
>NZ_CP011020.1|WP_047738254.1|4476568_4477444_-|helix-turn-helix-domain-containing-protein
MSELSQLFELAIRHSGNEDLGLLAYKSAHPGHLGVLGYAVMSSSTLGEAMARMVDHHSIIGTGFCMFFEGDETTVRIAGLSGNAQGEVLPRAFIDAVAAITLGLLRWLVPTVCITPVRAEFAYERPRDIRQLEQIFGHDLRFSCAANAMVFQKSDMDIAIATSDASLQQIHDQYLKRRLDEMRSENIAAATKKVILQHLVQARSLAMGDIVLTLGMSTHQLIRALEKENKSFQLLVDQVKKQHCYHLLVNTRLTLKQVSYSLGFRHSSALNKACERWFGMAPGACRSREKM
>NZ_CP011020.1|WP_042728240.1|4474775_4476407_-|methyl-accepting-chemotaxis-protein
MQLRRLKFAARIRFCFVLVIAALIGVSAFATYKAREIRQASLVVEQDALPGIALGDDIILAFSKTRFSVFRLLVSTDDLKLANNYNLLVADIREFEVAQAAYLPIISTDQERGLFTTIGKLFESYRTSALHVHDLIKRGSTGEATALVEGEMSSIAQNMVKVLGELEKLNDQAQQSASAAGQNAYETSIRVTLTAIMLVALGAIFLAHRLTVSISRPIAQALECANAIARGDLREPAQDASGNDEAALLLRAVMIMRKNLSDTLIDVYQAAGQLSNAAEELSVLVGSSNNDLQAQNSELEQAATAITEMSQAVDEVAHNAISTSDESRASLHLARDGQRELDSTLNAIARLDGSVNDASQRADILASNTVEISKVLEVIRSVAEQTNLLALNAAIEAARAGEAGRGFAVVADEVRSLAHRTSTSTMDIERMISHIQNGTQETVSALNDSAVQAAQTREQAASANKALQGITTTVSSIDERNTMIATACEEQALVAKDVDRSIIRIRDLSNLSAVRSDQTMAASEELAHIATKLKERLDGFNFG
>NZ_CP011020.1|WP_042728242.1|4474157_4474424_+|YebG-family-protein
MAVETLYRSTRDLETTFVDRKLADAHDQMLELAELLTDVLMKNVPGLSEKHAEDASIYMAKNRAIFAAAFKNNATALTELSAPAGSED
>NZ_CP011020.1|WP_042728243.1|4473206_4473707_-|PsiE-family-protein
MKINWAENLRQNVHQLAESLGNLFVETFHYLALFAIGAVTAWAAVMEFLQMIEAGHIKIDDILLLFIYLELGAMVGIYFKTNHMPVRFLIYVAITALTRLLISNVSHHSPPDLGIIYLCGGILLLAFAILVVRYASSQFPSVKIENPHRKVGAGSSEHAEVEKGEI
>NZ_CP011020.1|WP_042728244.1|4472892_4473210_+|DUF3509-domain-containing-protein
MDNPFQIITDAFAPHYQINLSIQGLDGSIMLTLSKSGRIVAKRMISAQQRNDPERLRRLVQSIQFGIAIEQGHSAVAILEAMTGGDNIKLPPPHAQGATSSAAGL
>NZ_CP011020.1|WP_042728245.1|4471986_4472397_-|HPF/RaiA-family-ribosome-associated-protein
MQIQVNSDNHIQSSIRLEEWVRTTIESTLERYEEDLTRVEVHLRDENGDKPGPHDLRCQLEARPKGHQPVSVTHKADSLELAIEGAAAKLEHALEHLFGKLRGKRAAGAAPTESVALADALLEEEFLENERAALHG
>NZ_CP011020.1|WP_047738252.1|4471030_4471909_+|helix-turn-helix-transcriptional-regulator
MPTLQTLQVFQALASSPNARLEHSAELGDGMAAALWSNHHDARDYEAPTHHTLSCYIAGGTGTFRRERPATTGGPGKLCILPAGHESAWVINGDIRLAHLYFSPEQFALGCVTLLDREPRQVQLHEATFLDDPQQARRFRQLIALNWDEPGERLLTSSLAHDLLDHLLLSQVGQRQGLRLKGGLAAHQRRLLVEYIDSHLADAISLGQLAALCALSHYHFARMFRESFELPPHQYLLARRLARARQLLRSTSQPLGDVALACGFASASHFTNRFRQALGATPGEYRQAFLAR
>NZ_CP011020.1|WP_047738250.1|4469988_4470891_-|DMT-family-transporter
MNLSLYLLTVLIWGTTWIALKLQLGVVAIPVSIVYRFGLAALILFALLLLSRRLQVMNRRGHLICVAQGLCLFCINFMCFLTASQWIPSGLVAVVFSTATLWNALNARVFFGQRIARNVLLGGALGLSGLALLFWPELAGHHASPQTLLGLALALLGTLCFSAGNMLSSLQQKAGLKPLTTNAWGMAYGAMMLAAWCAFKGIAFDMEWNSRYIGSLLYLVIPGSVIGFTAYLTLVGRMGPERAAYCTVLFPVVALNVSAVAEGYQWTAPALVGLVLVMLGNVLVFRKPRPVAPNVALGAR
>NZ_CP011020.1|WP_047738255.1|4480127_4480769_-|maleylacetoacetate-isomerase
MELYTYYRSTSSYRVRIALALKGLDYQALPINLIAPPGGEHRQPAYLAINPQGRVPALRTDEGDVLVQSPAIIEYLEERYPQVPLLNADLAIRAHERGVAALIGCDIHPLHNVSVLNKLRQWGHDEGQVTEWIGHWISQGLAAVERLIGDEGFCFGATPGLADVYLIPQLYAAERFNVSLQAYPRICRVAGLAAGHAAFQRAHPANQPDTPAG
>NZ_CP011020.1|WP_047738258.1|4480778_4482083_-|fumarylacetoacetase
MTQLSPVRSWVASANGHADFPLQNLPLGIFSHQGGTRRGGVAIGEQILDLSAALQAGLFDGAARAAVEAMAGGDLNGFFELGRGARVALRERLLELLREDSPQRAQLEAQQSQWLFPAADCQLHLPARINDYTDFYVGIEHAQNVGKLFRPDNPLLPNYKYVPIGYHGRASTIRPSGTDVRRPKGQTLPAGQAEPTFGPCARLDYELELGIWIGQGNALGEPIAIGDAAEHIGGFCLLNDWSARDIQAWEYQPLGPFLSKSFLTSISPWVVTAEALEPFRRAQPARPQGDPQPLPYLLDARDQAGGAFDIELEVLLLTDAMREQNLPAHRLTLSNTQYMYWTVAQMVAHHSVNGCQLQAGDLFGSGTLSGPQNGQFGSLLEITEGGKKPIELASGEVRRFLEDGDEIILRARCRREGFASIGFGECRGKILPAR
>NZ_CP011020.1|WP_047738259.1|4482086_4483391_-|homogentisate-1,2-dioxygenase
MNLDSPASDLAYQSGFGNEFASEALPGALPVGQNSPQKAPYGLYAELFSGTAFTMARSEARRTWMYRIRPSANHPAFTPLERQLVGGPLGEVTPNRLRWNPLENPAQPTDFLDGLVRMAANAGMDKPAGISIFHYCANRSMERVFFNADGEWLIVPQLGRLRIITELGVLELAPLEIAVLPRGLKFRVELLDAQARGYLAENHGAPLRLPDLGPIGSNGLANPRDFLTPVAHYENLAQPTTLVQKFLGQLWACELGHSPFDVVAWHGNNVPYKYDLRRFNTIGTVSFDHPDPSIFTVLTSPTSVHGLANLDFVIFPPRWMVAEKTFRPPWFHRNLMNEFMGLIQGAYDAKAEGFVPGGASLHSCMSAHGPDGETCTKAINAELQPAKIDHTMAFMFETSQVLRPSRFAMDCPQLQTDYDGCWASLPVTFDPTRR
>NZ_CP011020.1|WP_042729376.1|4483543_4484365_+|IclR-family-transcriptional-regulator
MQTPLNNGKQKVRSAEVGTDILKALAELSPSTSLSRLAEHVQMPASKVHRYLQALIASGFAEQNTATNHYGLGREALRVGLAALNGMDVLQVAAMPLAELRDDLNETCFLAVWGNHGATVVRIEPAVRAVTVVTQLGSVLPLLSSSTGLVFSAYLPERETIGLREQEVQGSERHALADDQAYATLCEQIRNRGLHHVHGLLMPGVDALSAPVFNAVGQVTAVMTIVGPTSLFHADENGPAAQRLLAATRAVSWRMGYETDGRSAQEVGDDPDQ
>NZ_CP011020.1|WP_047739533.1|4484329_4485031_-|hypothetical-protein
MNTQTFSTYSERLLALKLTRVDFAVQVLLGDHLEALGLNPHNLYLNTVAGFPEPQVETSRTLFDETLACVQKQTLAHYTQGITNIFSKRYSFAVEDRVKALDLITFEKIVADIVTGLAEKPGMDLSERPILPLSAEALHGALKVHLPGVDLEKVFITSFVNHDVANPVVFSSEPLVEYLLAHLRNNDIPYHAKGDPQAIYLVPFSGEERHLHPRLTPAHLNDLLIRIVPDFLG
>NZ_CP011020.1|WP_047738261.1|4485152_4487702_-|helix-turn-helix-transcriptional-regulator
MTAMTPCPDRPGLLPRLSSTHVPRRSLSEPLLTSEARVKLLCAPAGSGKSALFAECFLKAPADCRLHWLPLGGVALTPAQMGERLAQTLGLPVMDEAGLLAHLARLQTPTWLFLDDYCRVPNPELDQWLDRLLNTSSPALHLWLNGRRRPHCNWPRLLLDDELHEFDTQALVFSPGDVQQLLRHLPGPQAARTAREVIQRSGGWCAGVRISLLERCEWARSHATPGRPGTLADYLEYELFSALSPDLAQAWRVLAHLPRFNARLCEHLFGDTVGVECLPLLKDLGCFIEPWEHSSDWLQIFPALARLVREEPWPQGRSWHRRACQWFAAEQDWPMAFEQAMLAHEFETAVSVLQHLSFEHLLQGRNVVLLLNLHDQQGEALSLGTPQSVGLVTAALLFAGRFDQAAVCIEQLTRFAPQPRACQQRQLIARWQVLRGWLLHLSGDGDPAREHFLQAQAHLDPQAWASRLLCQSGLTQQALLKGDLASAQWINRQALCLARAEGSLVFEGLLELDHAQVLEQRGAPHRADELLGDVQARLDKPGQDFSPLLGRIALRRGRLALRMGFEERAAEQFQAGLETGLRSQDKQVLYGFLGKASLAANQGDYGEAFMQLRDAERIMQQRHIPDTVYRGVLLQISCQFWLQQGRAELAHEALTRVLRHFRGPQAKHAPPATLELIPRLEYLLLLTEVHLHRAQDPMARLEAMIAQARYAEMHGLETELHLALAEVAWLTADRSQARVLVQEGLERVACWRAQQALCELRLRQPELLHWAQSSGPIEPPAAPEDALLSHRELEVLELIAQGYSNQQIAERLFISLHTVKTHSRRIHSKLGVQRRTQAVAKAKVMGMMG
>NZ_CP011020.1|WP_042729378.1|4487887_4489255_-|DUF1329-domain-containing-protein
MRKMILQCGALALSLLAANVMAAVSPEEANKLGTTLTPLGAEKAGNADGSIPAWTGGIPKNAGAVDSKGFLADPFANEKPLFTITAATVDKYKDKLSEGQVAMFKRYPETYKIPVYPTHRSVALPPEIYESAKRSALNVTSINDGNGLANFTGNRYYAFPIPKNGVEVLWNHITRYHGGNLRRIITQATPQTNGSFTPIRFEEEVAVPFLIKDADPEKASNVLTYFKQEVTAPARLAGNVLLVHETLDQVKEPRLAWIYNAGQRRVRRAPQVAYDGPGTAADGLRTSDNFDLFSGAPDRYDWKLVGKKEMYIPYNSYKLDSPTLKYDDVIKAGHINQDLTRYELHRVWEVVGTVKPSERHIYAKRHMYIDEDSWQAAVVDHYDGRGQLWRVAEGHAQFYYDHQNPGYTLEALYDIIAGRYIALGMKNEEKHSYEYGFEARAADYTPAALRSSGVR
>NZ_CP011020.1|WP_042729379.1|4489277_4491071_-|DUF1302-domain-containing-protein
MTTITMRAIFKPQALAAAVALGCCAQAQAVSFNIGEIEGQFDSSLSVGASWGMRDADKDFVGTVNGGRGQSSTGDDGRLNFKKGETFSKIFKGLHDLELKYGDTGVFVRGKYWYDFELKDENREFKDISDSNRKEGAKSSGAEILDAFVYHNYSIADLPGTVRAGKQVVSWGESTFIGNSINSINPIDVSAFRRPGAEIKEGLIPVNMLFASQGLTDKLTLEGFYQLEWDQTVVDNCGTFFGNDVVADGCTTGYTVGSPAIAPFQPLTALFGQGIQVSREGVIIPRGGDRDARDSGQWGTALRWLGDDTEYGLYFMNYHSRTPTVGTTTAGASTLAALPGMVAIANGLAPGSGSGLAQSVMLGRGQYYLEYPEDIRLYGASFSTTLPTGTAWTGEISYRPNAPVQLSTNDLTLALVNPIAGGAASPIATRPGADNTGYRRKEITQVQSTLTHFVDQVWGADRLTLVGEAAVVHVGGLESRDKLRYGRDSVFGQYGFNGDTDGFVTSTSWGYRARAILDYSNVIGGVNFKPNVSWSHDVAGYGPNGLFNEGAKAVSLGVDADYRNTYTASLSYTDFFGGDYNVLKDRDFLALSFGVNF
>NZ_CP011020.1|WP_047738264.1|4491588_4492500_-|SDR-family-oxidoreductase
MNESVRFEDKVVIVTGAGGGLGRAHALLFARHGAKVLVNDLGGSAQGEGANASAADRVVAEIRAAGGIAEANHDSVIDGDKLVQNALDAFGRVDVVVNNAGILRDKTFHKMDDADWDLVYRVHVEGAYKVTRAAWPHLREQNYGRVIFTASTSGIYGNFGQSNYGMAKLGLYGLTRTLAIEGRKNNILVNAIAPTGGTRMTEGLIPPQVFEQLKPELVSPLVVYLASEACQETSGLFEVGGGWMGKVRWERSLGAGFNPRTGFSPEDVAAHWQQICDFEDAVHPNDNLEALKEMMANLQRYAV
>NZ_CP011020.1|WP_042729381.1|4492872_4493775_-|alpha/beta-hydrolase
MPLAQIPLRIWRQRSQIFLFRGHAIRYWVAGQGEPLLLIHGFPTASWDWHYLWQPLAQRYRVITCDMLGFGDSAKPADHTYSLLEQADLQQALLAHLNVRQGVHVLAHDYGDSVAQELIARHYEARLNVASCVFLNGGLFPETHRPVLAQKLLLSPLGWLLGRAFSRQSLVKSFRQIFGPRTGPTESVLDDFWSLIEAHHGPRIMHKLIAYIPERRVQRDRWVQAMQRDDVPLRVIDGALDPISGEHMVARYESLIPNPDTVLLSEIGHYPHTEAPVQVLKHYLAFRENIAPRCRKVAYS

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Crispr_ID: NZ_CP011020_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP011020_3

5919197-5919335

Unclear

Consensus_repeat	Method
CATTCTTGGCATATTCGCTTCCTGTATCCTTGGAAGCTTTCAGCGT	CRISPRCasFinder

1 spacers

cas3

The CRISPR arrays of NZ_CP011020_3

>merge|NZ_CP011020|3|5919197-5919335|CRISPRCasFinder
CATTCTTGGCATATTCGCTTCCTGTATCCTTGGAAGCTTTCAGCGTAGCAGAGGAATGAAAAATAAATCTGTCCCCTTTTTCTGTTTTCGCCGCATTCTTGGCAGATTCGCTTCCTGTATCCTTGGAAGCTTTCAGCGT

>NZ_CP011020|3|3|5919197-5919335|CRISPRCasFinder
CATTCTTGGCATATTCGCTTCCTGTATCCTTGGAAGCTTTCAGCGT	AGCAGAGGAATGAAAAATAAATCTGTCCCCTTTTTCTGTTTTCGCCG
CATTCTTGGCAGATTCGCTTCCTGTATCCTTGGAAGCTTTCAGCGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011020.1\|WP_042727861.1\|5910079_5910679_+\|putative-adenosine-monophosphate-protein-transferase-Fic	unknown	unknown	gnl\|CDD\|182396
NZ_CP011020.1\|WP_042732417.1\|5917813_5918398_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_047739207.1\|5911553_5912030_+\|SMI1/KNR4-family-protein	unknown	unknown	gnl\|CDD\|378155
NZ_CP011020.1\|WP_042731679.1\|5935586_5936933_-\|DEAD/DEAH-box-helicase	cas3	cd09639_cas3_CAS-I	gnl\|CDD\|236877
NZ_CP011020.1\|WP_042731675.1\|5942755_5943070_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_080964379.1\|5919860_5933120_-\|filamentous-hemagglutinin-N-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|293785
NZ_CP011020.1\|WP_047739211.1\|5919447_5919858_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_080964377.1\|5916723_5917155_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_053007417.1\|5912715_5913861_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_144419472.1\|5914099_5914927_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP011020.1\|WP_047739213.1\|5937126_5938425_+\|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl\|CDD\|223740
NZ_CP011020.1\|WP_123579870.1\|5909909_5910080_+\|DUF2559-domain-containing-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_042732913.1\|5935068_5935341_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011020.1\|WP_047739214.1\|5938541_5939408_-\|DMT-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP011020.1\|WP_042731674.1\|5943120_5944044_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP011020.1\|WP_053007418.1\|5914817_5916329_-\|calcium-binding-protein	unknown	unknown	gnl\|CDD\|380205
NZ_CP011020.1\|WP_047739206.1\|5910743_5911466_+\|phosphoprotein-phosphatase	unknown	unknown	gnl\|CDD\|277367
NZ_CP011020.1\|WP_042731676.1\|5942004_5942604_-\|FMN-dependent-NADH-azoreductase	unknown	unknown	gnl\|CDD\|224103
NZ_CP011020.1\|WP_047739212.1\|5933144_5934851_-\|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	unknown	unknown	gnl\|CDD\|225387
NZ_CP011020.1\|WP_047739205.1\|5908521_5909742_-\|putative-DNA-modification/repair-radical-SAM-protein	unknown	unknown	gnl\|CDD\|188431

Protein	Function_ID	Function_description	E-value
NZ_CP011020.1\|WP_042727861.1\|5910079_5910679_+\|putative-adenosine-monophosphate-protein-transferase-Fic	gnl\|CDD\|182396	PRK10347, PRK10347, putative adenosine monophosphate-protein transferase Fic.	8.53533e-58
NZ_CP011020.1\|WP_047739207.1\|5911553_5912030_+\|SMI1/KNR4-family-protein	gnl\|CDD\|378155	pfam09346, SMI1_KNR4, SMI1 / KNR4 family (SUKH-1). Proteins in this family are involved in the regulation of 1,3-beta-glucan synthase activity and cell-wall formation. Genome contextual information showed that SMI1 are primary immunity proteins in bacterial toxin systems.	6.54173e-17
NZ_CP011020.1\|WP_042731679.1\|5935586_5936933_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|236877	PRK11192, PRK11192, ATP-dependent RNA helicase SrmB; Provisional.	2.25425e-139
NZ_CP011020.1\|WP_047739213.1\|5937126_5938425_+\|mechanosensitive-ion-channel-family-protein	gnl\|CDD\|223740	COG0668, MscS, Small-conductance mechanosensitive channel [Cell envelope biogenesis, outer membrane].	5.33055e-29
NZ_CP011020.1\|WP_042731674.1\|5943120_5944044_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	4.50873e-37
NZ_CP011020.1\|WP_080964379.1\|5919860_5933120_-\|filamentous-hemagglutinin-N-terminal-domain-containing-protein	gnl\|CDD\|293785	sd00046, FHA_bHelix, beta-helical repeat found in filamentous hemagglutinin and related adhesins and CdiA family proteins. This model contains ten copies of an approximately 20-residue repeat found in two-partner secretion (TPS) proteins, including the filamentous hemagglutinin (FHA) family of adhesins and CdiA family proteins. These repeats form a right-handed beta-helical structure, and are found in large secreted proteins from a number of plant and animal pathogens. FHA family adhesins bind to various types of cells and may contribute to attachment, aggregation, and pathogenesis. CdiA proteins are involved in contact-dependent growth inhibition (CDI).	1.92939e-29
NZ_CP011020.1\|WP_144419472.1\|5914099_5914927_-\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	2.06453e-08
NZ_CP011020.1\|WP_047739214.1\|5938541_5939408_-\|DMT-family-transporter	gnl\|CDD\|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	2.77583e-56
NZ_CP011020.1\|WP_047739205.1\|5908521_5909742_-\|putative-DNA-modification/repair-radical-SAM-protein	gnl\|CDD\|188431	TIGR03916, hypothetical_protein, putative DNA modification/repair radical SAM protein. This uncharacterized protein of about 400 amino acids in length contains a radical SAM protein in the N-terminal half. Members are present in about twenty percent of prokaryotic genomes, always paired with a member of the conserved hypothetical protein TIGR03915. Roughly forty percent of the members of that family exist as fusions with a uracil-DNA glycosylase-like region, TIGR03914. In DNA, uracil results from deamidation of cytosine, forming U/G mismatches that lead to mutation, and so uracil-DNA glycosylase is a DNA repair enzyme. This indirect connection, and the recurring role or radical SAM protein in modification chemistries, suggest that this protein may act in DNA modification, repair, or both. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP011020.1\|WP_053007418.1\|5914817_5916329_-\|calcium-binding-protein	gnl\|CDD\|380205	NF033203, entero_EhxA, enterohemolysin EhxA. Members of this family are the RTX toxin called enterohemolysin or EhxA, because it is found in enterohemorrhagic Escherichia coli (EHEC) strains such as O157:H7.	2.19225e-08
NZ_CP011020.1\|WP_047739206.1\|5910743_5911466_+\|phosphoprotein-phosphatase	gnl\|CDD\|277367	cd07424, MPP_PrpA_PrpB, PrpA and PrpB, metallophosphatase domain. PrpA and PrpB are bacterial type I serine/threonine and tyrosine phosphatases thought to modulate the expression of proteins that protect the cell upon accumulation of misfolded proteins in the periplasm. The PPP (phosphoprotein phosphatase) family, to which PrpA and PrpB belong, is one of two known protein phosphatase families specific for serine and threonine. This family also includes: PP1, PP2A, PP2B (calcineurin), PP4, PP5, PP6, PP7, Bsu1, RdgC, PrpE, and ApA4 hydrolase. The PPP catalytic domain is defined by three conserved motifs (-GDXHG-, -GDXVDRG- and -GNHE-). The PPP enzyme family is ancient with members found in all eukaryotes, and in most bacterial and archeal genomes. Dephosphorylation of phosphoserines and phosphothreonines on target proteins plays a central role in the regulation of many cellular processes. PPPs belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	3.3273e-73
NZ_CP011020.1\|WP_042731676.1\|5942004_5942604_-\|FMN-dependent-NADH-azoreductase	gnl\|CDD\|224103	COG1182, AcpD, Acyl carrier protein phosphodiesterase [Lipid metabolism].	7.84014e-97
NZ_CP011020.1\|WP_047739212.1\|5933144_5934851_-\|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	gnl\|CDD\|225387	COG2831, FhaC, Hemolysin activation/secretion protein [Intracellular trafficking and secretion].	3.25165e-140

>NZ_CP011020.1|WP_042732417.1|5917813_5918398_-|hypothetical-protein
MTVSQSVLDDLWRGEKSICFFVHAGKCYWVVDEKYNFSLDAEKDYRAYLDSGEITQEQYEQSCKSFRGGILKMTAENFPQYLGDSSGKILSPSDLNDFIGADFEVFEKVEYYFLTGEGLTQDLFKRANMIHSRFPRFYINFDRKIFMHMDDARVHEGLAYPDWIAECFDFSFLIPASERYWVVAGNDYWKLRFV
>NZ_CP011020.1|WP_080964377.1|5916723_5917155_-|hypothetical-protein
MEMDDEFLEVNDLDWFAVFNDGLLAHFATGGRGVVPEVIRESISDYEMAYEFFCSLSDGFECEVVEENIPDFNIKVQRDRYLKSFAAMARKGLFSYDVCDAGYKLIARPKGGMKDSKLPLNIKGVLYKIPVGSFDNIKIIKVC
>NZ_CP011020.1|WP_053007418.1|5914817_5916329_-|calcium-binding-protein
MVAAGLNQTGTAGADALVGFNGNDNIHAGAGNDTLDAGTGTNQLFGDAGDDVIQVAYNSRDNILAGGTGNDTLTGGYFSDTYLFNLGDGQDTISEYDAGFSGIDTLRFGAGILASDIQAYKSGADVVFMHNNGTDQVRIKGWFDGTTSSASVVTQSVLERIEFADGTVWSFSDISSISLGQVGTELGDVLAGGSGNDNIRGGDGDDIIDGGAGVNRLYGDAGDDSIQVASSSRDNILAGGTGKDTLKGGYFSDTYVFNLGDGQDTITEYDAGNSATDTLRFGSGILASDIVMRRVGSDLVLLHRNGSDQVTVKEVFDRDTSAASAVTSTLIERIEFADGTTWTWSDMVAAGLSQTGTAGADNLVGFNGNDIIHGGSGNDTLDGGAGTNQLFGDAGDDVIQVAYNSRDNTLAGGTGSDTFTGGYFSDTYIFNLGDGQDTITEYETGRSAMDSRRFGSGNLAGDIVMRRTGSDCSRTRGLSEISKTTATNAGRNTPQRLRSDPCG
>NZ_CP011020.1|WP_144419472.1|5914099_5914927_-|IS4-family-transposase
MVLTVHEREGCPKYQKRLLQTLAEILPKDCVPILVADAGFRRPWIKAVEAQGWYYVGRVRNRDLYRNDADTWVPVKSLYALASSSPKSLGRIEMTQSAPHIIHLYCVRHSAKGRKHQRVTGSIAKNKLSRQSANREREPWLLASNLPEDQWNPSKIVAIYKQRMQIEEGFRDVKSEYFGVGITRHRSRCPRRIEVLLLISALANYIICLTGLQARQAGHERRFQSNSLKRRRVLSLWRLGLEYWRSGRGSNSRSTLERLEHALRAEVHQEAQALE
>NZ_CP011020.1|WP_053007417.1|5912715_5913861_-|hypothetical-protein
MSESKVGSFFKTVAMWLFFALFLAIGLAAMFTSLASGLIMLLAACVFVPQINRTIKEKAGVTVSPGHRAVAAIVCLGFMFYTSSKALDAERSERQAQEAQVAQVKAEQAQKEKHNYVSANKDSILAEMNVLIANQDYLGATALGAKYSNAGSFEIDQAFSKVLFQKTEADKQQKKVSLQASLAKIKQDDYRSLSSTYTQLAAIDSSYQANADKFTKLAEQQAQEAKVREQAAAEKARNRSLGLNWNYADDEDNMSGKPVRRAYVSSISTVDFKFPYSGTQRATLTIRKHPRWGTSVYIAIEKGQFVCGYDGCDVRVRFAKGNAQRMSASEPDDQSSDLLFISNASSFINQARKSDKVYIEADFYQEGSRIFEFDISDLDWK
>NZ_CP011020.1|WP_047739207.1|5911553_5912030_+|SMI1/KNR4-family-protein
MHEQPQTHRIHELLTLVGLRVAPQVAATFRPPATHADITRIEQTLGAPLPPSLAQLLLWHDGQEWNAPLRDSDNRRLLAAHEIVEVMTFFLDPEEEFLEPWGRYWVPFLTNDSGDYVVVDASPTGSGELIAYWHDWENRDVEHHSLLEWAQGLVEELG
>NZ_CP011020.1|WP_047739206.1|5910743_5911466_+|phosphoprotein-phosphatase
MNTISTFPSNPEGRDFVVGDVHGHFKLLSILLERSKFDVERDRLFSVGDLIDRGPDSLEVLDWLSQPWFHAVRGNHEQMLIDCIGGDGDIPRHTRNGGAWLYELPPPVQHELSKALQALPWIIEVDLPDGNTVGIVHAEAPQTQKGDDWQTAKAALQGQLGEICRLRALSMALYARERIEEQNSEPIKGIHQLYVGHSTVPSVKRLGNVIYIDTGCSFGDGALSLIELNSETVTHLRMSP
>NZ_CP011020.1|WP_042727861.1|5910079_5910679_+|putative-adenosine-monophosphate-protein-transferase-Fic
MPDKYGVGEDAYCYPGSTILRNKLDIRDESTLSEAEQQLSAIAADNVEFSPPPYSLGYLQGIHQVLFCDLYEWAGQLRTVGMAKQDTRFCQPSFMEAQAGKIFKGMAAQNWFEGMGRADLINAVAEAYSEINVIHPFREGNGRAQRILFEHLIMNAGFEISWWGIEKEQWIDANIAAYHCMLEPMQHVFEKCIGSPIRP
>NZ_CP011020.1|WP_123579870.1|5909909_5910080_+|DUF2559-domain-containing-protein
MGTVSLEAKKAYAARTRRSNYAASLRLEGFKVSFSESDCKMPTREEVLKTFTKTRA
>NZ_CP011020.1|WP_047739205.1|5908521_5909742_-|putative-DNA-modification/repair-radical-SAM-protein
MQLIAKLGILADAAKYDASCASSGAPKRSSRGRDGLGATDGMGICHSYTPDGRCVSLLKVLLTNFCLYDCQYCVNRRTSNVPRARFTPEEVVRLTLDFYRRNCISGLFLSSGIIRSADYTMEQLVRVARLLREDHQFRGYIHLKTIPDADPLLIEEAGRLADRLSVNIELSSEASLKRLAPEKQLTTIRQAMGTIHDGQQAVAGEARAPRFAPAGQSTQVIVGADATDDHAILQNAESLYQGYGLRRVYYSAFSPIPDSPASVPLAAPPLLREHRLYQADFLMRGYGYKAGELLGNAGNLDLDIDPKLAWALANREVFPLDVNRAEPALLARIPGIGLRSVQRLVALRRERRVRYDDLVQLRCVLEKARPFIITSDYRPAEAQVRSGLLRARLRDPQRPVQMGLWG
>NZ_CP011020.1|WP_047739211.1|5919447_5919858_-|hypothetical-protein
MKSFEYYTSLPDSMTNKELEVEFTELLDGFELQAVKRGDFIKSILELSDRQWHTYNVLDGGIRERIEYCLISVWDGYDQALVEDIIGIMVRLGLEKIWGFLCSCSLMDVSPEVFNEISLALSEVGDSVKDPYRGMR
>NZ_CP011020.1|WP_080964379.1|5919860_5933120_-|filamentous-hemagglutinin-N-terminal-domain-containing-protein
MDDRQYAFLARQPSAALQTRERFCGMPKRGLAFLLANVMFWQPMWAQADGIAVSAAGTGLDRAGNGVPIVNIARPNGNGLSHNQFTDYNVGSNGVILNNATARTQATQLGGIILGNPNLSGTAATTILNEVNGGNPSQLRGYTEVAGQSARVIVANPYGITCNGCGFINSPQVTLSTGKPVVENGRLDRYQVDQGSVIVEGAGLNATNVDRFEIITRSARINAEIQAKNLTIVAGRNDVNADTLNATARADDGSAKPQLAIDSSALGGMYAGAIKLVGTEAGVGVKLDGKLIASGGDIQLDANGQLSLAETSATGAVNVKAASATVQGAVYAGTALNVQTQGNLSNQQTLAARDSITLNAGGQLTNSGMIEAGVNADNTRNAAGDVSLTAQSLSNEGKSVVASRNLTANVTQTLSNQGGTQSGGQTTTVNAATLDNQNQGRVLSNNTLNITANTLLNTQGTISSNGNLTANVGQLNNNSGEFTGLNGVTLRVASLDNVAGLVAAGQGLVINASGQVNNRSGRLTSSKSVQLGAASMDNTAGRLLSDGALTASLSAQLLNQAGLLSSAGLLTLNAASLDNRQNGVVTTTQAADVNVGKVDNRGGELSSQGALTLTGTELDNSNSGKLIAYGDLRLTLERLGNQSQGVISSRSALAVNAGQLDNRQGSLYARQGMNLDLSGQLLNAQGSIKGDTSANVKAAGITNDAGQLTSVGALNIDSAATLSNLGGSVISGDTLLLKAGQVNNASGRIASAKALNASVTGLAQQNGQLVSNTRLSLDLNHGQLSNQGGLISTPGALLLNNLAAVDNRGGEISSDKAFSLNASALDNRAGKVVSKQGLNLTIAQALNNAQGRISANGLAVRAASLDNSSGTLSSDADLSVNLDAALTNLAGEVSSAGLTRLNAMTLNNRNGQVLGDNALEITLGGALDNREGVLGSGKVVDIQAAGLNNSGGGQLISDGSLRARISGLLDNQSQGEVIAKGALDLQTGSLDNRSGRLTGKDLLTLRSDSLDNRGGNVRADKALQLTVAQLDNRNNGVITGKTQVTVESTRLDNSGGLLSSVGPLTLKADEVQNGLGRISSQTDLTAVIDTLQQQGGALVAQGNLSLTGSVLDNRNGGLVGTTKALDLQVGQIDNRMGELSAGLGVKVGAQRLDNSDGGKLIAGNALELKVAQLINQTKGLIHAQGGLTLTGSTLDNSAGSLSSLEALVITLDNALLNNKGLISSEGALTVNAGSLDNTAGSLGSAGALSLLSTGGLINQGGSISTDAALTLNSASLDNSQKGLVSGSAATEVRTGAFNNSQGGRLTSGNTLTLTATQVNNAAGRIASSQALSASVTGLDQQQGELFSNTRVSLDMNQGQLNNQGGLINAPGLLLLSNLKDVNNQGGEISSRLAFTLAARNLDNSGGKLLSNQGLMLRTVQALNNAKGIISAASVDSHSASLDNRDGLISSLDQLDLTVDTLLDNQRGSLIADGALVLNADRLDNRTASIAGKAGLDVTVTALDNRQGTLVSTTDLTLKASSLDNRQAGLIGATKALDLKVDDLDNRGGELSGNTGVTLVSKNLDNSDSGQLFAGQTLKLTVDKLVNRNKGLLSAKAQLNLDGASLDNSGGYLISQQNQRIELSGDLINTQGQLSSEGTLDVSAANLSNTGGSLSSAANLTVKSLGRLDNQGGELVTDGALLLTSTALDNRQQGSISGKGAVNVTTGAFDNSQNGRLNSGSTLSLNAAQVTNQDGGRIGSQGALTASVSGLDQQGGQLFSNTSLSLDLNNGQLNNQNGLINAPGTLLLKNLLGVNNQGGEISSAQAFTLAAQSLNNDGGRLLSNQGLTLRIAQALNNVKGLIGAATVDAHAQSLNNNGGTLTSRSNLVLAIDQQLDNQAQGLISAAQLLTLNSGDLNNQGGSVLASGALLLNAMALNNSANGLINAQGDLTLTANALDSSDGGEVSAKGDMHLTLAALTQNGGRLLGEQAMALNLGGHDLNNRNGLITAKGPLTLNGLRNLNNQSGEISSSQSFTLSGQTLDNSGGKLISSQSLSLDGDSLVNQSGLISGWQDLQVSGSSLDNRNNGTLSSRNGDVGVTLSAALLNGAAGALVSQKKLTVSAASLDNRGGILSSGADQTLTVTGGLLNNAQGGLIDSGATLVMNAMTLGNANGTLNAQNALSFTGTSLDNSGGNLIGNAAVTLDLLGALTNTNGKLASVGPLRVERATQINNQGGQIASQGLLTLLTGGLDNRNRGTVAANDQLILNTTGTVQNDADGLIYSQNSGVQIDAASLGNGKGVVQSQGALTLTVTGDIDNQSGRLQAKAGDVAVVGRNLDNRGGVLASLQGLLTTQLSGVLKNGYDLNNNRQGGITQAQRLNLIALGGLDNYGGRISAQTGDATVTTRNFDNRNGGLYAKGKVNVTGNDFDNSGDNDGQIAGSQIDLNLTGALNNRLGIIESDSTLAIKAASLDNQTGQLRALGGSGTTNFQIGGLFDNRNGTLETANNGLILNAANFQNLGGSLLHVGSGDFDISTANLTNAGGSLVTRGGLTLTADSWTNSSVIQAGRLTVNVNNLTQTGTGQLLASTRLVGSGGNWSNDGLIASDGSINLTLGGSYVGNGRMSSLGGIDLTAAQLSLGAASSIAGGGDSTVTIGGQLSNAGRLTSSANLTVQAGNLINAGTLGSARNLVLKTPSLLNDRGLVFSGADMTLGVSNFTNQSGDLYGLGNVLIGGYGAAARAASVNNVSGSMESGGTFTINADGFQNRTEGAVASGGRKLISGFIANICNDCKGDYYTFTLAAREVFESVDNDTSASSLLTAGKDFVFQGSSFLNSKSTVSAGGNINIVADNVQNIGAQNGTIERTRMYQVAGMSDGGTGRFFANVLTPYNQRNNPDFPYVYYLDLDGNIHKAIPKSTRYREGGRDGESFSVVSLTDADTGGTVKTRGDYNLVLPGLAYGFENTTQSQYDPNNLLQMPNLDQYNLLSDIEIAKDSSGTASTVGSRNAVIQAGGNVSITATKDLQNSVIHEDYTASGGTNKVANTQASGTGTTIVRINNQLPPDRAQQQVNPLSLPGFALPTGQNGLFRLSGQGGSAQQATQANSGSPNWSMGSASISTSQRQQDLPDTQARAVQVGAIAAVGASDRQLSLIARQANDSDVSASTLNVSAPAQDSHSLPMPSRNSSSAGTQVAAVNVTGTNLLPTAQVVPQVGNVVDTPAASQTVARVQGVPETSFKANPQKYLIETNPVLTDLKSFMSSDYLLQNLGYDPDQSAKRLGDGLYEQRLIQQAVVARTGQRFIDGQTSDEGLFKYLMNNAIASKQELGLSVGVTLTSEQVAALTHDIVWLEEHEVNGEKVLVPVLYLAQTEGRLGPTGALIAGNDVTLIAGQNLDNVGTLRASNNLSATAGNDLVNSGLIEAGNRLDVLAVNNIANQAGGILAGRDVSIKAVMGDVVNERTVTTANDSRRQDFMDSAARIEAVNDLDMGAGRDFKSVGSVMVSGRDTTIDAGRDAIIASAQQESASNNGVRKSAVTQFGSSAQAGRDLAVNAGRDFTAIASQLGAERNVALTAGENMTISSATDETHSYSKTKKVTTQEDHVKQIGSAISAGGDVTMGAGKDMAIISSRISAGDEAYLVAGENLDVLAAQDSDYSLYDKKKKGSWGKKQTKHDEVTKVTNVGSEITAGGDLTLVSGDDQRYQAAKLNSGADLTVQSGGAITFEGVKDLSQETHTKSKSSMAWNSMKGKGHTDETLIQSQLVAQGDLVIKAVDGLNIDIKNINQKTVSETIDAMVKADPQLAWLKEAEQRGDVDWRLVKETHESFKYSSSSLGQGAMLAIIIIVTVLTAGAASAAVGSAAGATAGSGTAMAAAGSSAMVSAGTAVGTAAAGTGNLIASAALTSVASTAAVSTINNKGNMGAVFKDVFSSENLKGYVLAGASAGIASQFGFSPTDLKFDIPSAQSVAIKVAADAAAKTVITGGSLKDNLVTSALGSAISIGGAVSANKIGDITVFDNGKLSKVVMHAALGGLMAEAMGGDFRTGAIAAGANEALVDALADKLLPVGVDRNSPEYQQGVSKLLGASQLIGVLTAAFTGGDASAAAAVTANATQYNNLNHQSAERLLKELQGCRATEGCSAQNIREIVGKYEELSAQRSMAINACESRACVEAIQQSAVSLDAPVAKDLMDFLRRNVSYDMAGLLTGNPGAVAVPSQGVDGWGALFTSDKQMAFAKSLKEGWLTPDEWAGVDQWVKETSWLDQQAGRQLSLFERAGLLTELKTTLSMEILGKSPVVVGVNVPKGGATEQATPPSSKPESPASQADGDFGYLNQPVNKTAAFFDAYASAKGFINNGRISAADLEKLVPPGTQNSFKPSGTIADGSKFQYIWNGQKVEIKWHAPDANAAAKFPGSNAGSGWTAQIKIGNKLLGQDGLLYRQPSNATHIPVDF
>NZ_CP011020.1|WP_047739212.1|5933144_5934851_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein
MSSPAHWARLCLALLCLSPLTDARAAPTPGETDLIRERQNRLLEEQQRRLEELKDLPGQEAKPAQPTAPVDARCFPIKTIELKGADSLSASERERLLKPYIGQCLGVTQLNELLKVITDRYIEKGLVTSRAYLPQQDLSGGHLSVLVVEGRLEGLEGAENSQLSDRELAMAFPGKAGDLVNLREIEQMVDQLNRLPSNQAKMELTPGQNVGGSEVRVTNDPRKPWRAGLSRSNDGQRSTGEQQWGSSFEWDSPLGLADQLMLRGGHDAMTDHQHTSNNAMLYYNLPFGWWNVSYTYSQSEYRSQIAANGFNFKQTGDSQNHQLRVERVIHRDALSKTSLNTGLAYLRSNNFIEDSKLAVSSNRLSEAQFGINHGRRVGSAFINLDLGMQQGIGAFDAQDNNSPGPGQADARYRKYTATASYLLPFKLWNESFSFSSLMTGQRSEDVLFSPQRISLGGQSSIRGYKDQSLSGDSGGYWRNDLRWSRPISQAWLRPVFAEYGASLGYDQGVIRGDRYNGDQHGRMSSNSAELFARGEHLTASVTFAHSLERPDPLTEREAPIYFRLDVLL
>NZ_CP011020.1|WP_042732913.1|5935068_5935341_+|hypothetical-protein
MKTFLKLTLATTLACALPAWACTPEEATAKREQLAQEVTRLTQQNPAKAKEINDELQAMDLKTASKDLPDKCQLIDKRLQELKEAQQKAG
>NZ_CP011020.1|WP_042731679.1|5935586_5936933_-|DEAD/DEAH-box-helicase
MFSEFALHERLLKAVAELKFVEPTPVQAAAIPLALQGRDLRVTAQTGSGKTAAFVLPILNRLIGPAKVRVSIKTLILLPTRELAQQTLKEVERFSQFTFIKSGLITGGEDFKVQAAMLRKVPDILIGTPGRMIEQLNAGNLDLKEVEVLVLDEADRMLDMGFAEDVQRLVDECANRQQTMLFSATTGGSGLREMVAKVLNNPEHLQLNAVSQLNSTTRQQIITADHNQHKEQIVNWLLANETYEKAIVFTNTRAMADRIYGRLVAQEYKAFVLHGEKDQKDRKLAIDRLKQGGVKILVATDVAARGLDVDGLDMVINFDMPRSGDEYVHRIGRTGRAGNDGLAISLICHGDWNLMSSIERYLKQSFERRTIKEVKGTYSGPKKVKASGKAVGVKKKKVDGKGDKKKAAAKSPTKRKTANRPKADAPSLVSKDGMAPLKRRKPEAPAAE
>NZ_CP011020.1|WP_047739213.1|5937126_5938425_+|mechanosensitive-ion-channel-family-protein
MDIKQLWVHLQDLWGALDQHPLLHSGLGLMLLLVIALVLGRVARYLILHAAKLLGRQPALHWINDLRQNKVFHRLAQTTPSLIIQFGLHLVPELSKASLVFLGNVATAFTILFMVLALSALLSALLDVYARTEHARTRSIKGYVQLTKMVLYVFAAIIIVATLIDRSPLLLLSGLGAMSAVILLVYKDTLLSFVASVQLTSNDMLRVGDWIEMPQVGADGDVVDITLHTVKVQNFDKTIVSIPTWRLMSESFKNWRGMQQSGGRRIKRSLFIDASGVRFLHDEEEQRLTQVRLLTDYISRKQAELKAWNEAQGNVAAMSANRRRMTNLGTFRAYALAYLKSHAEIQPNMTCMVRQLQTTAQGIPLEIYCFTRTTVWADYERIQGDIFDYLLAVMPEFGLNLYQQPSGTDLRSGLLPAALGASHLPEPQKQVV
>NZ_CP011020.1|WP_047739214.1|5938541_5939408_-|DMT-family-transporter
MGYLLFVTLIQAFSFSLIGEYLAGHVDSYFAVLVRVVLAGLVFIPLTRWRQVEPSFMRGMLLIGALQFGVTYVCLYLSFRVLTVPEVLLFTILTPLHVTLIEDALNRRFNPWALIAALVAVAGAAVIRYDRINPDFFMGFLLLQLANFTYAAGQVLYKHLVARHPSDLPHYRRFGYFYLGALAVALPAFLLFGKADFWPEAPLQWGVLLFLGLVSTALGLYWWNKGACLVNGGTLAVMNNLHVPVGLLLNLLIWNQHEALGRLLLGGSVILAAVWISRLGVRQPLPAH
>NZ_CP011020.1|WP_042731676.1|5942004_5942604_-|FMN-dependent-NADH-azoreductase
MSRVLIIESSARQQDSVSRQLTQTFINQWKAAHPADEIKVRDLAVNPVPHLDANLLGGWMKPAEQRNDSENASLERSDQLTEELLAADVLVMAAPMYNFAIPSTLKAWLDHVLRAGVTFKYTPTGPQGLLTGKRAFVLTARGGIHAGGSTDHQEPYLRQVMGFIGIHDVTFIHAEGMNLGGDFQEKGLNQANAKLSQVA
>NZ_CP011020.1|WP_042731675.1|5942755_5943070_-|hypothetical-protein
MKKICCAVLALLPLTAFAYPIDVEKHLNGLSIDYNAYDTDADIGSIQVNNYGNTDAACTVVFRNGPEAPRTRKLEVAAGKFKNATAKFNRNIIKLRIVLTCQPK
>NZ_CP011020.1|WP_042731674.1|5943120_5944044_+|LysR-family-transcriptional-regulator
MKAPRVTLDQWRTLQAVVDHGGFAQAAEVLHRSQSSVSYTVARMQDQLGVPLLRIDGRKAVLTEAGGVLLRRSRQLVKQASQLEDLAHHMEQGWEAEVRLVVDAAYPSARLVRALTAFMPQSRGCRVRLREEVLSGVEEVLLEGVADLAISSFNIPGYLGAELSDVEFVAVAHPEHALHRLNRELSFQDLESQLQVVIRDSGRQQPRDVGWLGAEQRWTVGSLATAATFVSSGLGFAWLPRHMIERELKEGTLKRLPLDQGGSRNPSFYLYSNKEKPLGPATQILVELLRTFDTAPLDAPFAAPEQA

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

849802 : 883753

Klosneuvirus(50.0%)

holin

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_042729645.1\|849802_851506_-\|holin	choline dehydrogenase	A0A1V0SI18	Klosneuvirus	6.5e-50	29.7
WP_047735897.1\|851724_853197_-	betaine-aldehyde dehydrogenase	NA	NA	NA	NA
WP_042731602.1\|853277_853898_-	transcriptional regulator BetI	NA	NA	NA	NA
WP_042731603.1\|854120_855299_-\|holin	choline ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	1.0e-25	37.9
WP_042731604.1\|855295_856141_-\|holin	choline ABC transporter permease subunit	NA	NA	NA	NA
WP_042731605.1\|856211_857159_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_042731606.1\|857583_858960_+	L-serine ammonia-lyase	NA	NA	NA	NA
WP_042731607.1\|859543_860647_+	GlxA family transcriptional regulator	NA	NA	NA	NA
WP_047735898.1\|860691_860955_-	hypothetical protein	NA	NA	NA	NA
WP_042731609.1\|861254_862418_-	gamma-butyrobetaine dioxygenase	NA	NA	NA	NA
WP_042731610.1\|862437_862914_-	4-hydroxybenzoyl-CoA thioesterase	NA	NA	NA	NA
WP_047735899.1\|863089_864055_-	L-carnitine dehydrogenase	NA	NA	NA	NA
WP_042732673.1\|864194_865082_-	3-keto-5-aminohexanoate cleavage protein	NA	NA	NA	NA
WP_042732674.1\|865152_866097_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_042732675.1\|866264_867224_+	GlxA family transcriptional regulator	NA	NA	NA	NA
WP_047735900.1\|867292_868468_+	hypothetical protein	NA	NA	NA	NA
WP_047735901.1\|868614_869031_-	DUF3010 family protein	NA	NA	NA	NA
WP_042732527.1\|869089_869491_-	DUF1311 domain-containing protein	NA	NA	NA	NA
WP_042732528.1\|869727_870705_+	membrane dipeptidase	NA	NA	NA	NA
WP_030139308.1\|870917_871448_+	hypothetical protein	NA	NA	NA	NA
WP_042732529.1\|871463_873524_+	dimethylglycine demethylation protein DgcA	NA	NA	NA	NA
WP_047735902.1\|873687_875637_+	dimethylglycine demethylation protein DgcB	NA	NA	NA	NA
WP_047735903.1\|875636_876857_+	electron transfer flavoprotein subunit alpha/FixB family protein	NA	NA	NA	NA
WP_047735904.1\|876872_877643_+	electron transfer flavoprotein subunit beta	NA	NA	NA	NA
WP_052497384.1\|877792_879196_-	hypothetical protein	NA	NA	NA	NA
WP_047735905.1\|880300_883753_+\|holin	choline dehydrogenase	NA	NA	NA	NA

DBSCAN-SWA_2

3032277 : 3077052

Pseudomonas_phage(84.62%)

tail,holin,tRNA,plate

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042732363.1\|3032277_3033993_+\|tRNA	proline--tRNA ligase	NA	NA	NA	NA
WP_042732362.1\|3034010_3034964_+	lipoprotein	NA	NA	NA	NA
WP_047736983.1\|3035134_3036196_-	DNA polymerase IV	NA	NA	NA	NA
WP_042731516.1\|3037018_3039661_+	bifunctional lysylphosphatidylglycerol flippase/synthetase MprF	NA	NA	NA	NA
WP_047736986.1\|3039660_3040953_+	virulence factor family protein	NA	NA	NA	NA
WP_047736988.1\|3041245_3043147_-	potassium transporter Kup	M1HZV6	Acanthocystis_turfacea_Chlorella_virus	1.0e-75	34.3
WP_042731513.1\|3043421_3044762_+	30S ribosomal protein S12 methylthiotransferase RimO	NA	NA	NA	NA
WP_047736990.1\|3044986_3045460_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_047736992.1\|3045542_3046253_+	RNA-binding protein S4	NA	NA	NA	NA
WP_042730783.1\|3046309_3046771_+	DUF1456 family protein	Q9EYF4	Enterobacteria_phage	2.5e-36	50.0
WP_047736993.1\|3046839_3047538_+\|tRNA	tRNA (N6-threonylcarbamoyladenosine(37)-N6)-methyltransferase TrmO	NA	NA	NA	NA
WP_003198368.1\|3047740_3048520_-	ferredoxin--NADP reductase	NA	NA	NA	NA
WP_042730781.1\|3048641_3049568_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_042730780.1\|3049572_3049935_-	diacylglycerol kinase	NA	NA	NA	NA
WP_042730779.1\|3050006_3050660_-	response regulator transcription factor	NA	NA	NA	NA
WP_042730778.1\|3050853_3051600_-	DTW domain-containing protein	NA	NA	NA	NA
WP_042730777.1\|3051784_3052207_+	quorum-sensing-regulated virulence factor family protein	NA	NA	NA	NA
WP_042730776.1\|3052234_3052432_-	hypothetical protein	NA	NA	NA	NA
WP_047736995.1\|3052683_3053802_+	TIGR00730 family Rossman fold protein	NA	NA	NA	NA
WP_047736997.1\|3053846_3054314_-	recombination regulator RecX	NA	NA	NA	NA
WP_042730773.1\|3054322_3055375_-	recombinase RecA	A0A2D1GPX2	Mycobacterium_phage	5.0e-109	60.7
WP_042730772.1\|3055458_3055959_-	CinA family protein	B5TK85	Pseudomonas_phage	7.9e-81	92.8
WP_047737000.1\|3056030_3056567_-	lysozyme	B5TK84	Pseudomonas_phage	1.8e-70	80.3
WP_042730770.1\|3056548_3057112_-	glycoside hydrolase family 19 protein	B5TK83	Pseudomonas_phage	8.6e-92	88.7
WP_047737003.1\|3057133_3057568_-	hypothetical protein	B5TK82	Pseudomonas_phage	2.3e-52	69.3
WP_047737005.1\|3058518_3059028_-	hypothetical protein	B5TK78	Pseudomonas_phage	7.8e-68	80.5
WP_047737008.1\|3059024_3060188_-	hypothetical protein	B5TK77	Pseudomonas_phage	7.2e-202	90.7
WP_047737009.1\|3060199_3060799_-	DUF2313 domain-containing protein	B5TK76	Pseudomonas_phage	1.7e-109	96.5
WP_047737011.1\|3060786_3061827_-\|plate	baseplate J/gp47 family protein	B5TK75	Pseudomonas_phage	2.5e-177	93.1
WP_042732290.1\|3061816_3062215_-	phage GP46	B5TK74	Pseudomonas_phage	6.5e-70	96.2
WP_042732291.1\|3062214_3062724_-\|plate	phage baseplate assembly protein	B5TK73	Pseudomonas_phage	1.0e-83	94.7
WP_047737013.1\|3062848_3063889_-\|plate	baseplate protein	B5TK72	Pseudomonas_phage	3.1e-188	94.5
WP_047737014.1\|3063892_3065131_-	2-hydroxyacid dehydrogenase	B5TK71	Pseudomonas_phage	2.0e-221	94.9
WP_047737016.1\|3065117_3066692_-\|tail	tail protein	B5TK70	Pseudomonas_phage	1.3e-142	87.6
WP_042732988.1\|3066822_3067119_-\|tail	phage tail assembly protein	B5TK69	Pseudomonas_phage	3.5e-44	95.9
WP_042732987.1\|3067115_3067463_-\|tail	phage tail protein	B5TK68	Pseudomonas_phage	9.7e-62	99.1
WP_047737021.1\|3067529_3069026_-\|tail	tail sheath protein	B5TK67	Pseudomonas_phage	3.5e-265	94.0
WP_042729844.1\|3069025_3069208_-	DUF2635 domain-containing protein	B5TK66	Pseudomonas_phage	4.1e-27	98.3
WP_047737023.1\|3069204_3069789_-	hypothetical protein	B5TK65	Pseudomonas_phage	2.2e-82	78.9
WP_042729842.1\|3069892_3070243_-\|holin	pyocin R2, holin	B5TK61	Pseudomonas_phage	1.9e-52	90.4
WP_042729847.1\|3070300_3070882_-	DUF642 domain-containing protein	NA	NA	NA	NA
WP_080964315.1\|3070886_3071075_-	Com family DNA-binding transcriptional regulator	B5TK59	Pseudomonas_phage	1.3e-15	97.4
WP_042729841.1\|3071543_3072278_-	helix-turn-helix transcriptional regulator	B5TK58	Pseudomonas_phage	3.6e-130	94.3
WP_047737026.1\|3072813_3073167_+	hypothetical protein	B5TK57	Pseudomonas_phage	1.9e-49	88.9
WP_042729846.1\|3073326_3074052_+	Zeta toxin	NA	NA	NA	NA
WP_047737028.1\|3074472_3077052_+	DNA mismatch repair protein MutS	A0A1V0SDQ0	Indivirus	6.9e-27	23.6

DBSCAN-SWA_3

3236572 : 3242857

uncultured_Caudovirales_phage(83.33%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042732610.1\|3236572_3236965_+	sulfurtransferase complex subunit TusD	A0A2H4JA39	uncultured_Caudovirales_phage	4.2e-53	77.5
WP_047737188.1\|3236964_3237327_+	sulfurtransferase complex subunit TusC	A0A2H4J8C0	uncultured_Caudovirales_phage	1.2e-38	65.8
WP_047737190.1\|3237326_3237620_+	sulfurtransferase complex subunit TusB	A0A2H4JG28	uncultured_Caudovirales_phage	6.3e-30	64.6
WP_042732606.1\|3237616_3237952_+	TusE/DsrC/DsvC family sulfur relay protein	A0A2H4J8B6	uncultured_Caudovirales_phage	2.1e-45	81.1
WP_047737192.1\|3237948_3238950_+	glycosyl transferase family protein	A0A2H4JBY5	uncultured_Caudovirales_phage	2.4e-161	82.4
WP_047737194.1\|3239038_3240043_+	glutathione S-transferase family protein	NA	NA	NA	NA
WP_047737197.1\|3240181_3241576_-	uroporphyrinogen-III C-methyltransferase	NA	NA	NA	NA
WP_042731100.1\|3241576_3242857_-\|tRNA	serine--tRNA ligase	A0A1B1IVT2	uncultured_Mediterranean_phage	2.8e-98	46.1

DBSCAN-SWA_4

3661737 : 3668793

Escherichia_phage(66.67%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_042728070.1\|3661737_3662859_-	DegT/DnrJ/EryC1/StrS family aminotransferase	E5ES42	Bathycoccus_sp._RCC1105_virus	4.0e-40	31.1
WP_047737568.1\|3662916_3663912_-	dTDP-4-dehydrorhamnose 3,5-epimerase	A0A291LA62	Escherichia_phage	3.1e-44	49.5
WP_047737572.1\|3663952_3665020_-	hypothetical protein	NA	NA	NA	NA
WP_042728073.1\|3665182_3666061_-	glucose-1-phosphate thymidylyltransferase RfbA	A0A291LA53	Escherichia_phage	1.9e-109	69.0
WP_047737575.1\|3666057_3666954_-	dTDP-4-dehydrorhamnose reductase	K7QJU0	Escherichia_phage	3.9e-30	35.1
WP_047737578.1\|3666950_3668027_-	dTDP-glucose 4,6-dehydratase	A0A1D7XFE8	Escherichia_phage	2.0e-97	53.0
WP_042728076.1\|3668235_3668475_-	LapA family protein	NA	NA	NA	NA
WP_042728077.1\|3668499_3668793_-	integration host factor subunit beta	A3E2K9	Sodalis_phage	1.9e-10	41.1

DBSCAN-SWA_5

6033965 : 6101270

uncultured_Caudovirales_phage(25.0%)

integrase,protease,transposase,tRNA

attL 6028116:6028130|attR 6098130:6098144

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
6028116:6028130	attL	NA	NA	NA	NA
WP_047739253.1\|6033965_6035534_-\|transposase	IS66 family transposase	A0A218MNE7	uncultured_virus	4.3e-125	48.9
WP_047739254.1\|6035615_6035951_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_080964383.1\|6035947_6036316_-	IS66 family insertion sequence hypothetical protein	NA	NA	NA	NA
WP_162489258.1\|6036215_6036683_-	hypothetical protein	NA	NA	NA	NA
WP_160310732.1\|6036900_6037056_-	hypothetical protein	NA	NA	NA	NA
WP_047739256.1\|6037054_6037765_+	hypothetical protein	NA	NA	NA	NA
WP_063854434.1\|6038188_6038956_+	hypothetical protein	NA	NA	NA	NA
WP_047739257.1\|6039154_6039706_-	TIR domain-containing protein	NA	NA	NA	NA
WP_047739258.1\|6039729_6041193_-	hypothetical protein	NA	NA	NA	NA
WP_047739259.1\|6041254_6041758_-	TIR domain-containing protein	NA	NA	NA	NA
WP_047739628.1\|6041788_6042955_-	restriction endonuclease	NA	NA	NA	NA
WP_047739260.1\|6043221_6043842_+	hypothetical protein	NA	NA	NA	NA
WP_047739261.1\|6043834_6044953_+	ImmA/IrrE family metallo-endopeptidase	B6SBZ6	Clostridium_virus	2.1e-28	30.5
WP_160310733.1\|6044982_6045135_+	hypothetical protein	A0A2H4J9J0	uncultured_Caudovirales_phage	1.0e-15	76.0
WP_047739262.1\|6045423_6046554_-	DUF4935 domain-containing protein	NA	NA	NA	NA
WP_144419474.1\|6047743_6048599_+\|transposase	IS5 family transposase	A0A0N9SHJ4	Paenibacillus_phage	3.3e-18	39.2
WP_047739267.1\|6049435_6049912_-	hypothetical protein	NA	NA	NA	NA
WP_047739629.1\|6049908_6050145_-	hypothetical protein	NA	NA	NA	NA
WP_047739268.1\|6050165_6050858_-	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_047739269.1\|6051366_6051585_-	hypothetical protein	NA	NA	NA	NA
WP_047739270.1\|6051736_6052045_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_047739271.1\|6052165_6052684_+	hypothetical protein	NA	NA	NA	NA
WP_080964384.1\|6052721_6052913_+	hypothetical protein	NA	NA	NA	NA
WP_047739630.1\|6053035_6054481_-	alpha/beta hydrolase	NA	NA	NA	NA
WP_047739272.1\|6054793_6056053_+	hypothetical protein	NA	NA	NA	NA
WP_047739273.1\|6056215_6057382_+	RNA-directed DNA polymerase	NA	NA	NA	NA
WP_047739274.1\|6057402_6058431_-	hypothetical protein	NA	NA	NA	NA
WP_047739275.1\|6058652_6058967_-	hypothetical protein	A0A2H4J9H6	uncultured_Caudovirales_phage	9.6e-08	42.0
WP_047739276.1\|6059216_6060947_+	AAA family ATPase	NA	NA	NA	NA
WP_047739277.1\|6060936_6062349_+	AAA family ATPase	NA	NA	NA	NA
WP_047739278.1\|6062659_6063712_+	hypothetical protein	NA	NA	NA	NA
WP_160310734.1\|6064226_6064376_+	hypothetical protein	NA	NA	NA	NA
WP_144419476.1\|6064857_6065343_-	hypothetical protein	NA	NA	NA	NA
WP_047739279.1\|6066431_6067916_-	hypothetical protein	NA	NA	NA	NA
WP_047739280.1\|6068272_6069577_-\|tRNA	serine--tRNA ligase	A0A1B1IVT2	uncultured_Mediterranean_phage	2.8e-93	52.6
WP_053007432.1\|6069658_6069886_-	hypothetical protein	NA	NA	NA	NA
WP_080964416.1\|6070083_6070548_-	hypothetical protein	NA	NA	NA	NA
WP_047739282.1\|6070941_6071289_-	hypothetical protein	NA	NA	NA	NA
WP_047739283.1\|6072202_6072658_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_144419477.1\|6073211_6074084_-	hypothetical protein	NA	NA	NA	NA
WP_047739284.1\|6074277_6075063_+	hypothetical protein	NA	NA	NA	NA
WP_047739285.1\|6075144_6075363_+	hypothetical protein	NA	NA	NA	NA
WP_080964387.1\|6075466_6076522_+	ParA family protein	NA	NA	NA	NA
WP_047739286.1\|6076778_6079442_+	AAA family ATPase	NA	NA	NA	NA
WP_080964388.1\|6079923_6080958_-	DNA-binding protein	NA	NA	NA	NA
WP_080964389.1\|6081138_6082179_+\|integrase	site-specific integrase	NA	NA	NA	NA
WP_144419478.1\|6083019_6084057_-	hypothetical protein	NA	NA	NA	NA
WP_144419479.1\|6084053_6084734_-	hypothetical protein	NA	NA	NA	NA
WP_053007422.1\|6084730_6085621_-	AAA family ATPase	NA	NA	NA	NA
WP_080964390.1\|6085641_6087516_-\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
WP_080964417.1\|6088285_6088663_-	cytochrome c	NA	NA	NA	NA
WP_047739290.1\|6088765_6089680_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_047739291.1\|6089789_6090542_+	SDR family oxidoreductase	Q06VL0	Trichoplusia_ni_ascovirus	2.3e-15	31.4
WP_047739292.1\|6090674_6092222_+	calcium-binding protein	NA	NA	NA	NA
WP_047739293.1\|6092970_6094401_+\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_047739294.1\|6094662_6096009_-	hypothetical protein	NA	NA	NA	NA
WP_047739647.1\|6096110_6097550_-	hypothetical protein	NA	NA	NA	NA
WP_047739648.1\|6097817_6098900_-	restriction endonuclease or methylase	A0A1S5SAB0	Streptococcus_phage	9.2e-66	40.2
6098130:6098144	attR	NA	NA	NA	NA
WP_144419499.1\|6099236_6099884_-	hypothetical protein	NA	NA	NA	NA
WP_053007424.1\|6099908_6101270_-\|protease	M48 family metalloprotease	NA	NA	NA	NA

DBSCAN-SWA_6

6147502 : 6224888

Shigella_phage(12.5%)

transposase,plate

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_144419424.1\|6147502_6148649_+\|transposase	IS3 family transposase	U5P429	Shigella_phage	8.0e-52	42.2
WP_080964392.1\|6148740_6149196_-\|transposase	transposase	Q75QL1	Wolbachia_phage	5.3e-15	36.4
WP_160310736.1\|6159158_6159299_+	hypothetical protein	NA	NA	NA	NA
WP_042730526.1\|6160833_6162939_-	elongation factor G	A0A2K9L6L3	Tupanvirus	6.4e-39	24.0
WP_024776462.1\|6162969_6163440_-	30S ribosomal protein S7	NA	NA	NA	NA
WP_003186084.1\|6163544_6163916_-	30S ribosomal protein S12	NA	NA	NA	NA
WP_042730527.1\|6164132_6168332_-	DNA-directed RNA polymerase subunit beta'	A0A2I7QNZ7	Vibrio_phage	2.0e-68	27.3
WP_042730528.1\|6168396_6172470_-	DNA-directed RNA polymerase subunit beta	A0A146JCU1	Tokyovirus	8.9e-21	30.6
WP_047739312.1\|6172689_6173055_-	50S ribosomal protein L7/L12	NA	NA	NA	NA
WP_003206099.1\|6173133_6173634_-	50S ribosomal protein L10	NA	NA	NA	NA
WP_003186095.1\|6173833_6174529_-	50S ribosomal protein L1	NA	NA	NA	NA
WP_003176435.1\|6174528_6174960_-	50S ribosomal protein L11	NA	NA	NA	NA
WP_010443972.1\|6175077_6175611_-	transcription termination/antitermination protein NusG	A0A291AUS6	Sinorhizobium_phage	1.7e-09	27.6
WP_003186101.1\|6175620_6175989_-	preprotein translocase subunit SecE	NA	NA	NA	NA
WP_080964395.1\|6176162_6176771_-	elongation factor Tu	NA	NA	NA	NA
WP_038443748.1\|6177141_6177891_-	pantothenate kinase	NA	NA	NA	NA
WP_038443749.1\|6177880_6178840_-	bifunctional biotin--[acetyl-CoA-carboxylase] synthetase/biotin operon repressor	NA	NA	NA	NA
WP_047739313.1\|6184869_6186090_-	CoA transferase	NA	NA	NA	NA
WP_039593369.1\|6186103_6187285_-	acyl-CoA dehydrogenase	NA	NA	NA	NA
WP_042731838.1\|6187441_6188341_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_042731839.1\|6188771_6189893_+	Re/Si-specific NAD(P)(+) transhydrogenase subunit alpha	NA	NA	NA	NA
WP_003187010.1\|6189908_6190232_+	NAD(P) transhydrogenase subunit alpha	NA	NA	NA	NA
WP_042731840.1\|6190231_6191668_+	NAD(P)(+) transhydrogenase (Re/Si-specific) subunit beta	NA	NA	NA	NA
WP_042731841.1\|6191869_6193363_+	acetyl-CoA hydrolase/transferase family protein	NA	NA	NA	NA
WP_047739314.1\|6193681_6193897_+	DUF1127 domain-containing protein	NA	NA	NA	NA
WP_047739315.1\|6194235_6194553_+	DUF2388 domain-containing protein	NA	NA	NA	NA
WP_042730545.1\|6194659_6194968_+	DUF2388 domain-containing protein	NA	NA	NA	NA
WP_003187020.1\|6194994_6195315_+	DUF2388 domain-containing protein	NA	NA	NA	NA
WP_047739316.1\|6195311_6197273_+	DUF4105 domain-containing protein	NA	NA	NA	NA
WP_042730547.1\|6197359_6198166_-	tryptophan synthase subunit alpha	NA	NA	NA	NA
WP_047739317.1\|6198165_6199398_-	tryptophan synthase subunit beta	NA	NA	NA	NA
WP_047739318.1\|6199511_6200429_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_047739319.1\|6200401_6200728_-	DUF883 domain-containing protein	NA	NA	NA	NA
WP_042730551.1\|6200881_6201097_+	dodecin domain-containing protein	NA	NA	NA	NA
WP_042730552.1\|6201211_6201436_+	DUF1161 domain-containing protein	NA	NA	NA	NA
WP_047739320.1\|6201489_6202491_-	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_042730554.1\|6202726_6203158_+	OsmC family protein	NA	NA	NA	NA
WP_047739321.1\|6203296_6203530_+	DUF1161 domain-containing protein	NA	NA	NA	NA
WP_047739322.1\|6203535_6203961_-	lipoprotein	NA	NA	NA	NA
WP_042730557.1\|6204002_6204416_-	hypothetical protein	NA	NA	NA	NA
WP_042730558.1\|6204475_6205567_+	aminopeptidase	NA	NA	NA	NA
WP_042730559.1\|6205653_6206952_-	MFS transporter	NA	NA	NA	NA
WP_003177184.1\|6207327_6207732_+	acyl-CoA thioesterase	NA	NA	NA	NA
WP_047739323.1\|6207788_6208688_+	D-hexose-6-phosphate mutarotase	NA	NA	NA	NA
WP_047739324.1\|6208746_6209679_-	serine/threonine protein kinase	T2AWK4	Cannes_8_virus	1.6e-10	28.1
WP_047739325.1\|6209675_6210401_-	serine/threonine-protein phosphatase	NA	NA	NA	NA
WP_047739326.1\|6210400_6213883_-	type VI secretion system membrane subunit TssM	NA	NA	NA	NA
WP_047739327.1\|6213896_6214760_-	DotU family type IV/VI secretion system protein	NA	NA	NA	NA
WP_047739328.1\|6214765_6216097_-\|plate	type VI secretion system baseplate subunit TssK	NA	NA	NA	NA
WP_042728891.1\|6216093_6216588_-	type VI secretion system lipoprotein TssJ	NA	NA	NA	NA
WP_080964396.1\|6216593_6217370_-	type VI secretion system-associated FHA domain protein TagH	NA	NA	NA	NA
WP_047739330.1\|6217589_6219107_-	sigma-54-dependent Fis family transcriptional regulator	NA	NA	NA	NA
WP_047739670.1\|6219117_6221703_-	type VI secretion system ATPase TssH	A0A1C3S747	Escherichia_phage	1.1e-88	32.4
WP_047739331.1\|6221715_6222720_-\|plate	type VI secretion system baseplate subunit TssG	NA	NA	NA	NA
WP_047739332.1\|6222683_6224471_-\|plate	type VI secretion system baseplate subunit TssF	NA	NA	NA	NA
WP_047739333.1\|6224477_6224888_-\|plate	type VI secretion system baseplate subunit TssE	NA	NA	NA	NA

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP011020

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection