CRISPRimmunity

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_CP011130	Lysobacter capsici strain 55 chromosome, complete genome	22 crisprs	DEDDh,csa3,WYL,cas3,RT,Cas9_archaeal,DinG	8	12	2	0

1. NZ_CP011130

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP011130_1

• CRISPR_ID: NZ_CP011130_1
• CRISPR_location: 116060-116140
• CRISPR_type: Orphan
• Repeat_type: I-E
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_1

Consensus_repeat	Method
CGTCATTCCCGCGAAGGCGGGAATCCAG	CRISPRCasFinder

spacers of NZ_CP011130_1

>1.1|116088|25|NZ_CP011130|CRISPRCasFinder
AGTCTTCAGCGTCATCTCTCCAGAT

CRISPR arrays and Neighbor proteins around NZ_CP011130_1

CRISPR arrays

The CRISPR arrays of NZ_CP011130_1

>merge|NZ_CP011130|1|116060-116140|CRISPRCasFinder
CGTCATTCCCGCGAAGGCGGGAATCCAGAGTCTTCAGCGTCATCTCTCCAGATCGTCATTCCCGCGAACGCGGGAATCCAG

>NZ_CP011130|1|1|116060-116140|CRISPRCasFinder
CGTCATTCCCGCGAAGGCGGGAATCCAG	AGTCTTCAGCGTCATCTCTCCAGAT
CGTCATTCCCGCGAACGCGGGAATCCAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_046658611.1|107105_107387_+|DUF2798-domain-containing-protein	unknown	unknown	gnl|CDD|378657
NZ_CP011130.1|WP_187313315.1|124069_125053_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776
NZ_CP011130.1|WP_057920326.1|113001_114453_+|efflux-transporter-outer-membrane-subunit	unknown	unknown	gnl|CDD|273830
NZ_CP011130.1|WP_046658615.1|120505_121756_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|182528
NZ_CP011130.1|WP_187313314.1|123086_124073_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|224482
NZ_CP011130.1|WP_082648219.1|108354_109575_+|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776
NZ_CP011130.1|WP_057920323.1|98847_102453_+|UvrD-helicase-domain-containing-protein	unknown	unknown	gnl|CDD|224000
NZ_CP011130.1|WP_057920332.1|126492_127020_+|hypothetical-protein	unknown	unknown	gnl|CDD|240273
NZ_CP011130.1|WP_057920333.1|127720_129610_+|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	unknown	unknown	gnl|CDD|235362
NZ_CP011130.1|WP_057920324.1|102449_104297_+|exodeoxyribonuclease-V-subunit-alpha	unknown	unknown	gnl|CDD|273631
NZ_CP011130.1|WP_057920327.1|115362_115791_-|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl|CDD|273970
NZ_CP011130.1|WP_082124635.1|105377_106538_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176114
NZ_CP011130.1|WP_057920329.1|121752_123069_-|hypothetical-protein	unknown	unknown	gnl|CDD|273776
NZ_CP011130.1|WP_046658610.1|104475_105279_+|type-I-restriction-enzyme-HsdR-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|372640
NZ_CP011130.1|WP_036103475.1|109838_113009_+|multidrug-efflux-RND-transporter-permease-subunit	unknown	unknown	gnl|CDD|223911
NZ_CP011130.1|WP_057920325.1|107383_108358_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|212491
NZ_CP011130.1|WP_046658616.1|125075_125750_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224059
NZ_CP011130.1|WP_051546930.1|116476_117229_-|hypothetical-protein	unknown	unknown	gnl|CDD|225837
NZ_CP011130.1|WP_057920328.1|117372_118191_-|hypothetical-protein	unknown	unknown	gnl|CDD|198057
NZ_CP011130.1|WP_082648220.1|118416_119445_-|pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|215524

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_046658611.1|107105_107387_+|DUF2798-domain-containing-protein	gnl|CDD|378657	pfam11391, DUF2798, Protein of unknown function (DUF2798). This family of proteins has no known function.	0.000168399
NZ_CP011130.1|WP_187313315.1|124069_125053_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	6.23371e-15
NZ_CP011130.1|WP_057920326.1|113001_114453_+|efflux-transporter-outer-membrane-subunit	gnl|CDD|273830	TIGR01845, Outer_membrane_protein_OprM, efflux transporter, outer membrane factor (OMF) lipoprotein, NodT family. Members of this model comprise a subfamily of the Outer Membrane Factor (TCDB 1.B.17) porins. OMF proteins operate in conjunction with a primary transporter of the RND, MFS, ABC, or PET systems, and a MFP (membrane fusion protein) to tranport substrates across membranes. The complex thus formed allows transport (export) of various solutes (heavy metal cations; drugs, oligosaccharides, proteins, etc.) across the two envelopes of the Gram-negative bacterial cell envelope in a single energy-coupled step. Current data suggest that the OMF (and not the MFP) is largely responsible for the formation of both the trans-outer membrane and trans-periplasmic channels. The roles played by the MFP have yet to be determined. [Cellular processes, Detoxification, Transport and binding proteins, Porins].	9.28413e-94
NZ_CP011130.1|WP_046658615.1|120505_121756_-|ABC-transporter-permease	gnl|CDD|182528	PRK10535, PRK10535, macrolide ABC transporter ATP-binding protein/permease MacB.	2.54656e-49
NZ_CP011130.1|WP_187313314.1|123086_124073_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl|CDD|224482	COG1566, EmrA, Multidrug resistance efflux pump [Defense mechanisms].	1.59176e-14
NZ_CP011130.1|WP_082648219.1|108354_109575_+|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	3.56996e-73
NZ_CP011130.1|WP_057920323.1|98847_102453_+|UvrD-helicase-domain-containing-protein	gnl|CDD|224000	COG1074, RecB, ATP-dependent exoDNAse (exonuclease V) beta subunit (contains helicase and exonuclease domains) [DNA replication, recombination, and repair].	0
NZ_CP011130.1|WP_057920332.1|126492_127020_+|hypothetical-protein	gnl|CDD|240273	PTZ00110, PTZ00110, helicase; Provisional.	0.00233612
NZ_CP011130.1|WP_057920333.1|127720_129610_+|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG	gnl|CDD|235362	PRK05192, PRK05192, tRNA uridine-5-carboxymethylaminomethyl(34) synthesis enzyme MnmG.	0
NZ_CP011130.1|WP_057920324.1|102449_104297_+|exodeoxyribonuclease-V-subunit-alpha	gnl|CDD|273631	TIGR01447, recD, exodeoxyribonuclease V, alpha subunit. This family describes the exodeoxyribonuclease V alpha subunit, RecD. RecD is part of a RecBCD complex. A related family in the Gram-positive bacteria separates in a phylogenetic tree, has an additional N-terminal extension of about 200 residues, and is not supported as a member of a RecBCD complex by neighboring genes. The related family is consequently described by a different model. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP011130.1|WP_057920327.1|115362_115791_-|nuclear-transport-factor-2-family-protein	gnl|CDD|273970	TIGR02096, putative_cyclase, conserved hypothetical protein, steroid delta-isomerase-related. This family of proteins about 135 amino acids in length largely restricted to the Proteobacteria. This family and a delta5-3-ketosteroid isomerase from Pseudomonas testosteroni appear homologous, especially toward their respective N-termini. Members, therefore, probably are enzymes.	9.58379e-43
NZ_CP011130.1|WP_082124635.1|105377_106538_-|LysR-family-transcriptional-regulator	gnl|CDD|176114	cd08422, PBP2_CrgA_like, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA and its related homologs, contains the type 2 periplasmic binding domain. This CD includes the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA and its related homologs. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.15975e-70
NZ_CP011130.1|WP_057920329.1|121752_123069_-|hypothetical-protein	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	8.95748e-11
NZ_CP011130.1|WP_046658610.1|104475_105279_+|type-I-restriction-enzyme-HsdR-N-terminal-domain-containing-protein	gnl|CDD|372640	pfam13588, HSDR_N_2, Type I restriction enzyme R protein N-terminus (HSDR_N). This family consists of a number of N terminal regions found in type I restriction enzyme R (HSDR) proteins. Restriction and modification (R/M) systems are found in a wide variety of prokaryotes and are thought to protect the host bacterium from the uptake of foreign DNA. Type I restriction and modification systems are encoded by three genes: hsdR, hsdM, and hsdS. The three polypeptides, HsdR, HsdM, and HsdS, often assemble to give an enzyme (R2M2S1) that modifies hemimethylated DNA and restricts unmethylated DNA.	7.28053e-06
NZ_CP011130.1|WP_036103475.1|109838_113009_+|multidrug-efflux-RND-transporter-permease-subunit	gnl|CDD|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_CP011130.1|WP_057920325.1|107383_108358_+|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.	2.89348e-12
NZ_CP011130.1|WP_046658616.1|125075_125750_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224059	COG1136, SalX, ABC-type antimicrobial peptide transport system, ATPase component [Defense mechanisms].	8.74663e-108
NZ_CP011130.1|WP_051546930.1|116476_117229_-|hypothetical-protein	gnl|CDD|225837	COG3300, COG3300, MHYT domain (predicted integral membrane sensor domain) [Signal transduction mechanisms].	5.32911e-37
NZ_CP011130.1|WP_057920328.1|117372_118191_-|hypothetical-protein	gnl|CDD|198057	smart00989, V4R, The V4R (vinyl 4 reductase) domain is a predicted small molecular binding domain, that may bind to hydrocarbons.	8.39997e-09
NZ_CP011130.1|WP_082648220.1|118416_119445_-|pyridoxal-phosphate-dependent-enzyme	gnl|CDD|215524	PLN02970, PLN02970, serine racemase.	1.74646e-139

Protein sequences

>NZ_CP011130.1|WP_057920327.1|115362_115791_-|nuclear-transport-factor-2-family-protein
MKIDGTRSHDRATELVLSYYAAFNRTDWDGMLATLGPQVVHDLNQGARETGVEAFAAFLQRMARHYREQLRDIVVMVSPDGTRAAAEYVVHGEYLVTDAGLPQARGQRYELPGGAFFEIRDGKIQRVTNYYNLEHWVAQVGA
>NZ_CP011130.1|WP_057920326.1|113001_114453_+|efflux-transporter-outer-membrane-subunit
MRNFKLPAIAVLTLALAACAVGPDYVRPTLATPDAFARADAQAGTDGTAAPEPGAEFWRGFNDPLLTRLVEESLTANHDLRIALANYDRANALLRGAKFDRFPTITGSASGSDTRSSSDQMPGVSNNGRDNESYSAQANVSWELDLFGRVRRNVESERAETWASAADLQAMQVSIVGEVARSYVELRGLQERLRVARENAENQTETLRLVQARFDAGRGTEFDTSRARAQLEATLARVPNLEAQVAVTEHRLAVLTGQTPDALIAELDKAVALPSLPQRLDAATPGELLRRRPDVAAAEHRLHAATARIGVATADLFPRFTLSGLIGSQAIDTSALFERASETRLVALGIDWSFLDIGRVRSRIKAADASAEGELARYQQSVLLALEDTENALVRYARARVEDQHLERASQDSLKAAKLARVRYEAGATDLFEVLDAERTQLQAQDAFADGRTRSVTGAIALYKAMAGGWPDREPVREGVARN
>NZ_CP011130.1|WP_036103475.1|109838_113009_+|multidrug-efflux-RND-transporter-permease-subunit
MDFSKFFIDRPIFAAVLSIVIFAAGLIAIPILPISEYPEVVPPSVVVRTVYPGANPKVIAETVATPLEEAINGVEDMMYIKSVAGSDGVLVTTVTFRPGTNADDAAVRVQNRVSQALARLPEDVRRQGVTTQKQSPVFLMVVHLTSPNGKYDTLYLRNYARLHVKDSLARLSGVGDAQIFGGGDYAMRAWLDPDKIASRGLTAGDVVRAMREQNVQVSAGQLGAEPIAKSDFLTLINAQGRLRSEKEFGDIVLKSGEGGEIVRLSDVARLELGAGDYSLRSQLDGKNAVGIGIFQAPGANALDIQEQVIANMDRIAKSFPEGIKYEAVYDTTIFVRDSIKAVVSTLLEAILLVVLVVILFLQTWRASIIPLIAVPVSIVGTFAALYLLGFSINTLSLFGLVLAIGIVVDDAIVVVENVERNIEEGLSPLEAAHQAMKEVSGPIVAIALVLCAVFVPMAFLSGVTGQFYKQFAVTIAISTVISAINSLTLSPALAARLLKPHGAPKDAPTRLIDRLFGWLFRPFNRFFASSSEKYQRSISGILGKRGAVFVVYAVLLVATGFMFKIVPAGFIPLQDKLYLIAAVKLPEGSSISRTDELLRKVTDVAMKTEGVQHSIAFPGLNAVQFTNTPNTGVAFLPLKPFGERSRSAVEITSEINQKIAGFQEGFTFALMPPPILGLGNGAGYQMFIEDRSNLGYGALQTAVSAFQGTIMQTPGMGYANSTYQANVPQLDAEVDRVKAKAQGVPLTELFDTLQTYLGSAYVNDFNQFGRTWQVIAQADGSFRDNVEDIANLRTRNDRGEMVPIGSMVSIKQTFGPDPVLRYNGYPAADIAGDVDPRVMSSAQAMDVVRDVAAKVLPHGMEIEWTDLSYQQASQGNAALIVFPLAILLAFLVLAALYESWTLPLAVILIVPMCMLSALIGVKLTGGDNNVFVQVGLVVLMGLACKNAILIVEFARELELQGKGIVEAALESCRLRLRPIVMTSIAFIAGTVPLVLSHGAGAEIRSVTGITVFAGMLGVTLFGLFLTPVFYVALRKMVGTKLVSHGDHHNASEKVHA
>NZ_CP011130.1|WP_082648219.1|108354_109575_+|efflux-RND-transporter-periplasmic-adaptor-subunit
MSTRNSPARSGRPGLGLSLLALTASVVIALAAVGCGSQAATPEGGAPPPPEVSVAQVLSKQVRQWDDFTGRVSAVESVELRARVSGYVDRVAFKEGQEVKKGDLLFVIDPRRYRAELNRAQAQLEQARAEARLAKTQDKRAQTLVEAKAISREEAETRRAATTQGDAAVRAAEAAVASAQLDLTFSEVRSPIDGRAGRAMVTVGNLASADQTVLTTVVSQNPMYVYFESDEQTYLRYNELARKGQREGNKNPVRIGLASETGYPHEGTVDFTDNQVDPTTGTIRARAVVDNADRVFTQGLFARVQLEGSAEFKAMLVDDKAVLTDQDRKYVYVLGPKNEAVRKDVVLGRMIQGLRVVESGLAPTDKVIVHGVQKVFFPGMPVSPKTIAMGAAAPLPAAPGAAAGAL
>NZ_CP011130.1|WP_057920325.1|107383_108358_+|SDR-family-oxidoreductase
MKAPLVVLGATGGVGRGVVQAAIDSGRPVIAVARQASELKALKAGYPHADLTTIAGSVSSDAAGAKLARALRKLDRPLAGVVAAVCGGAERGRLLDNPADFLRRKLDEDLLPHLAAARHLLPLLAQYDRGGTYVLIGGPGSEHPWAGYGHRSIGAAALRMLARVLHDEARQLAVRVQLLAVDSPVCTEFNQRHSCPEWPSALSVGQRVMALIDHEVSGEPPRAIVPYALRQPPPQLPPRSAARLPPSPASATASPPRSAADSYSTTTSRTSTPKTITATTASSDACPQDPGSPADEKTQRCLQDARALLKSLTSNNPKQEPTPR
>NZ_CP011130.1|WP_046658611.1|107105_107387_+|DUF2798-domain-containing-protein
MLTPRQARFAFLPLMLVAMSALIGLAVVVFRQGLSQGPEEAWMLAWVLAFTIALPAAMLLMPAISAVLAHYTRDDKRHAIIPRVGEKVPGAGQ
>NZ_CP011130.1|WP_082124635.1|105377_106538_-|LysR-family-transcriptional-regulator
MAHDLNDTLIFVKVVEAGSFISAARALRLPKTTVSRKVQELETRLGAQLLHRTTRKLGLTEAGNLYFEHCQRIARELAEAESAVGQLQGGPRGWLRITAPYSVGITWIAPLLGEFHARHPEVRVEMNLSNETVDMIDKGIDVALRVGDLPDSNLVARRLAIFRTQIYASPNYLARHGEPLHPDDLRHHRTLAMPKSRRNNEYVWTLSDGERNVDYVIDPVMVANDPGPLRGALLCGEALMLAADVTVKAFAEQGYVQRVLAGWTGPEYEFNAVFPRGQVQSPKVRAFVDFLVERLNFDADYMQVLCPDAKRFRKASEEAEAAMAHGLAKEAASEPRTIAVPVVEAIEAITEAVDKRAAKTPARVGKRGDEVERKDDTPSDEDAALV
>NZ_CP011130.1|WP_046658610.1|104475_105279_+|type-I-restriction-enzyme-HsdR-N-terminal-domain-containing-protein
MAAIPKKVSERLVAGLKRYQPILSAAKARDVGEADTVTIIKDMLADVFGYDKYSDVTSEHSIRGTFCDLAIKIDNQLQTLIEVKAIGLELKDQHVKQAIDYAANQGVDWVLLTNGITWRVYHLVFAKPIDQELVLEIDFCALSPRLESDIELLYLWCKEGWQRSMLGEYHIQKQALSRFFVGAMLQTDAVIDVVRRELRRVSPDVRIDSDQIRDVLIKEVIKREVIEGEKADEARKKIMKAANKALRATPVKPAKGKNAAEDQPASD
>NZ_CP011130.1|WP_057920324.1|102449_104297_+|exodeoxyribonuclease-V-subunit-alpha
MSLLEALHREGSLRTVDHAFAQALRRLDRDTPDAVLAAAALASQAIARGHAAFDPRSPQWLSEATTDWPDPEQWLALLADSRWVATPAPGIAASAHAPLVLERGLLYLRRYREYERRLADGLRRIAAFAPPPTDLAALAPLFALLFPNARDDDRQARAAALALLQSLLLATGGPGTGKTTTIARVLLLLIAQARLDGVSAPRIALAAPTGRAAERMAESLRAAALRLSALDGIDPSLCEALPTQASTLHRLLGSVPDSPRFRHDARNPLAFDVIVVDEASMVDLPLMCKLVEAVPAGARLILLGDRDQLPSVEAGDVLAAIVDAAGDDDGLPATLAQSLRPLLGEIAIQADPAPLSAYRVHLRRGYRQAESLELAPLAEATRAGDADTVLALLRGGELAGVQFHEDVHDPLAGAGRDWLLPAWRALAAIEDPLEALQAAARLRLLTALRDGGQGAAPLNARIEEALAGAHRPAYFHGRLLLITENSYRHGLFNGDIGICLRPRDADGRELANAATVAWFAGGSEGVRPFHPSALPAHSGAFAMTVHKAQGSEFDAVWLQLPRQDARHLSRELLYTGMTRARRELHIAGSEAVLRLALSRHAARVSGLSWRLAEER
>NZ_CP011130.1|WP_057920323.1|98847_102453_+|UvrD-helicase-domain-containing-protein
MSAVRDPFLDLPLDGLRLIEASAGTGKTYTLATLVTRLVIERGLRIGDILAVTFTDAATQELRERLRRRLLLAARIAADDPALIAAEDDGERAITRELVRAQAEHEGAAALRSRLQRAAREIDLAAVVTIHGFCARVLAEHALETGQPFAAPEMIGSERELIDEIAVDLWRAFGNDAGQAELLSLQWPAGPRALASDLGALMRAPVLLPSAPEPSPDPLPALQDAAESLRLAYEQHGAQAFDAIEAAMAAKVLNGQTWRATLPGQLRQALDRWCANGDPVEPIEPRIDRLTPAVLAEKTNKGKQAQTPSSPLFVAVERYLDVAAQRAQWLARQALRLVHDIRDAGRVRLAELKRVRRVQSFDDLIADVALALDGPHGEALAQRLREQYAVALVDEFQDTDVRQWRIFERVFGEATVMESGLGEPARAAGLFLIGDPKQAIYGFRGGDVHTYLSAAARAEAAPPLDHNFRSRPSVLRAISALYAQAGDTAFVDARIRFREVAPGGAVADADLQRDGAIAPALTIRRLPAPDDDRKKPEWSAPESRDLAVRACVASIHAWLRDAREGRASIDGRALQPGDIAVLVRSHDEAARIQQALIAAGIAAVAAGRRSLFATEQAIELLTVFDAVLHPGDGGRLRAALATVLIGLDGERIAALGLDEAEQAVWQAQALVWRERWQRHGPLALVSDLCAEHAPRLLALADGERRLTNLLQLGETLQEADTRSLGLHGLRDWLHLRIAEADDSDEKQQLRLESDARRVQILTLHKSKGLEFALVFLPFVAIGREPRGGRLCEYPDPLHGRVLQVQSEVFDPNAPDWDSARERAAIEARSEDARLLYVGLTRARHALWLASGPLYLAQASPLQAMLADADALAHQHPDAIVIDDAPLEHPPAPLPPPAAGAVPPARRARHSVPRDWWVYSFTQLTNEDDGAGQGALVADERGAEDEPDIAAAVLTPGDARYSGSRFGNVVHTALERVDFGAWREWTADAPAPDGEAAWLASALRGEGYTDADIDDGLPLLTSLVGLTLTAALPEGTRLCELPERERRSEMEFHFALESVPVDRLLATLHAHGWLRERQAFGLRRRLEGLMTGKIDLVYAFEGRYYVLDYKTNRLPSYDAIQVDRAMGESEYTLQSLIYTVALHRWLRFRLGDAYDYARDFGGVRYLFCRGLDPADPDAGLYAHQPARELVDAVDALFAGGAA
>NZ_CP011130.1|WP_051546930.1|116476_117229_-|hypothetical-protein
MPHDSAIQCIHDPLLVILSYVVSVLGSFTALQLAIAIPNATSAAHRWRAVAAAGLAMGGGAIWAMHFIAMLACQMNVEVTYDLPITLGSAVVAVVSCMAGLAIAGTGLFNWGKLIIAGVLMGLGVTGMHYAGMSAMLMAADTVYNSTLVMASAGIAIVASIVALWLAFNLRGWGQMLGSALVMGVAVCGMHYTGMLAASFVPNEARASLVAGGVSGGYLGVGIFVVTTALLAAVLTISLLRQRQRSMVRI
>NZ_CP011130.1|WP_057920328.1|117372_118191_-|hypothetical-protein
MVDVEFRVVSDRRDGLLLALGQVVIANGFTLLRQRMLNSEEGVVLVMVVRGPAEALLMLEERLGTHHLVQSFEASPYEPAPAAAPTPAPAARNGASTHAPAAAAPSANTAPAASYAAAPSATAAPIDTQRVETLLPQLARNYPNILLQLVALERELPPTQREATLRYIGQRVGAWVYKRDFALGGQLPLADSVRRIALPAMRQLVQAELHEDVLKVRNSPFCHRGETGECCHFLRGMLGGLLEGQHGADGVRVVESQCRNTGAESCRFEFEA
>NZ_CP011130.1|WP_082648220.1|118416_119445_-|pyridoxal-phosphate-dependent-enzyme
MNNLSAPHGVESASANPHTTSAEPVAPTYSDILAAAARIAPLAHATPVLRSRAIDELAGCELHFKCENLQRGGAFKFRGASNAVFSLSDEEVARGIVTQSSGNHGGAIALAARLRGATATVVAPHNTPQVKLAAIRAYGAQIVHCEPDQASRDATTAQVLAQTGGVLVHPFNDPRVIAGQGTATLELLAAAPTLDAVIAPVSGGGLLSGTAIAAHGHNPAIEVYGAEPEGARDAHDSLREGRRITGRKPDTICDGLRAELGTLTFPILRSHLRDILLVDDPQVIAAMRLIWERMKLVVEPSGAVPLAVVLANRERFANRRIGLIVSGGNVDLDLIAQWFARA
>NZ_CP011130.1|WP_046658615.1|120505_121756_-|ABC-transporter-permease
MNRALQWLPTIWREAIEELWRRRLRTLLTLLGLIFGVGAIVAMQAVGEGSRREALHLVESLGLNNLIAEAKPQDENTLRETRARSLGLSLADADAALAVVPGAERYAAEKPIRTHSVFSDNGRSDAQASGVSPDYFALSSLRIAKGRGLTDADDRALAAVAVLGHQAAADLFPGVDPLGRYLKVNHVWLEVIGVLADRDLSKDQFEGVQLGLESNRVYLPLASARARFKFQPQEDEIDRFLLRLQDPSQLATGARVLSTVLNQRHAGMADFRLVVPQQLFQQHQKTQRIFRVVMGAIAGVSLLVGGIGIMNIMLANVLERRREIGLLRALGARRRDVIAQFLREATVICVSGAALGLVFGIVLAYLIATFAGWQVAWAPIPVLLSALFCAAVGLAFGVYPARQAARLDPIAALRHD
>NZ_CP011130.1|WP_057920329.1|121752_123069_-|hypothetical-protein
MTCRNTLRYGALLCLPAMLIACGGEVAPAATETVASAPLNLSVRGEGELKSAKSTPLNVPGRNWAARQVEWMLPEGSAVKKGDLIARFSAEQGKQELAQTLIDLQRNELARAAKQGELETAQSKVAVDLAQVAVQLGIAERYATADLSTMARNEVLDAVQDKRFLSEKRDTLQWQRGQAGVRGQAELGVLDAQRATFDITAKARQSDLDALELRAPNDGVLMLSTNWSGDKPNVGATLRAGFDYGSLPDASAMELELSLPQIEAQGIKVGNAVEMFPVGRPEQKIVSKLSWVASAAKVRSQESPVKYLTMKARIPAEAIARYKLVPGQRLQARVILFDAPALSVANVAIDSDNGKEYVRVRNGADFLRRPVELGVRGPARSQVLSGLRAGDEVLLAEPGVVAAITAPSEPGEDAAAGKPATAEDAKAAPAAAGPAVRR
>NZ_CP011130.1|WP_187313314.1|123086_124073_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MSRAWCLLVLLVAATAPAIAAAPLRVDGEVYARRSSPLMPPSVERMWQFNITELATDGTPVKKGQPVIRFDSNDVIKQLTEKRSQLKEKQSELGKLDLELAERERSERLATAEAQSELEKAQRKTQQPVELIAGIEYRKLLVKRTQMERKMALARKREVLSAEQRRQERRLLSSELGQLQADVDRLQRSLAALNVIAPRDGLMMHRSNFEGEKYDVGSQVWVGQTVAEIPDMSTLAVRAELAERDLQRVAVGVPVRIVVEGGAGSVLSGKIASIGRAIRSKSQVQPVPVLDLDVQLDDPRAPLRPGQAVRVEIQSPGSGGATARKATR
>NZ_CP011130.1|WP_187313315.1|124069_125053_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MFALTMAALPAAAVVLTGEVRSVGGQTIYTPQSNSAPVAIRYFVPEGQPVKAGDVVLRIDPGQAGTQIPDLEAKIEQAHAKAAKELAELEVKQVDAEVALAEADAALATARIEAAIPRALISALDYDRHQGELDKTQRESKLKREQLDAARAAVARRKRDGELEVGKLEVQRDYYRVLLRQSEVRAQQDGIVVHGFNNNWIGGRIDEGSSTMPGSQAGAVVVDGGRMEVRAWALEPDRRGLRVGQNVQLSFDALPKQRVQGRIRNIAGAPDRKSEWGEGRYFSVDIDLPAAHGLRLLPGMSVRVTAATPPAPAAAATGATARSGAQR
>NZ_CP011130.1|WP_046658616.1|125075_125750_-|ABC-transporter-ATP-binding-protein
MIELDAVHRRYEMNGQAVNALAGVDLKIASGEFVAITGASGSGKSSLLNILGCLDRPTRGRYLIEGRDVAAMDDEAASDIRNRRIGFVFQSFHLLPRLSLLENVLLPLRFHREPPPGTHDRALALLQRVGLGERSNHRPSELSGGQQQRAAIARALLLQPALLLADEPTGNLDSKSAGDVLDLIQEVHAGGQTVVLVTHDRDLAARAPREVRLHDGKVDHDSAA
>NZ_CP011130.1|WP_057920332.1|126492_127020_+|hypothetical-protein
MIPLVAASLLAGCVSDYSLRGGGGGGSYYYGRPSVDYNYYGGYGGYYGPGYGYPYGEAYRYRGYGYPGYYGGGYYGGYPYGYYPRPYYPNRPGRPHNPSRPPNPPRQDGGVPWRDTHRVGGGAWAPNNPVQQQPQPRAYSTPQPRSFSQPQMQPRMPTAPSVRRDGGRAWKDVER
>NZ_CP011130.1|WP_057920333.1|127720_129610_+|tRNA-uridine-5-carboxymethylaminomethyl(34)-synthesis-enzyme-MnmG
MNDSFYRYDVIVIGGGHAGTEAALASARAGARTLLLTHSVETVGAMSCNPAIGGIGKGHLVKEIDALGGIMARAADAAGIQWRRLNASKGPAVRATRCQADRGLYRSFIRRAVEAQPGLTLFQAAVDDIVFDAGRVSGVLTQTGLRFHAPAVVLTAGTFLAGKVHVGQTTYAAGRAGDPPATALAARLREGPFVVDRLKTGTPPRIDGRSLDYSVMEEQPGDDPRPVMSFLGTQADHPRQVSCWITHTSERTHEIIRGALDRSPLYTGQIEGIGPRYCPSIEDKVVRFAEKASHQIFVEPEGLDVAEIYPNGISTSLPFDVQLDLVRSIRGFENAHITRAGYAIEYDFFDPRGLKSTLETKAVAGLFFAGQINGTTGYEEAAAQGLLAGVNAARFVRGNEGWSPRRDEAYLGVLVDDLITHGTLEPYRMFTSRAEYRLQLREDNADLRLTPTGHELGLVDEARWSAFERKREAIERESARLASVWAAPNNALGREIAQTLGIEVSRECSARDLLKRPELDYAKLMQVPSLGPAVDAAEVAEQVEIGVKYAGYLDRQREEIERQQRNESTAIAEDFDYAAVRGLSLEVQQKLERVRPQTVGQAQRIPGMTPAAISLLLVHLTRARRSRVA

Crispr_ID: NZ_CP011130_2

• CRISPR_ID: NZ_CP011130_2
• CRISPR_location: 162025-162105
• CRISPR_type: Orphan
• Repeat_type: I-E
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_2

Consensus_repeat	Method
CGTCATTCCCGCGAAGGCGGGAATCCAG	CRISPRCasFinder

spacers of NZ_CP011130_2

>2.1|162053|25|NZ_CP011130|CRISPRCasFinder
AGACTTCAGCGCCATTCCACCAGAA

CRISPR arrays and Neighbor proteins around NZ_CP011130_2

CRISPR arrays

The CRISPR arrays of NZ_CP011130_2

>merge|NZ_CP011130|2|162025-162105|CRISPRCasFinder
CGTCATTCCCGCGAAGGCGGGAATCCAGAGACTTCAGCGCCATTCCACCAGAACGTCATTCCCGCGAAAGCGGGAATCCAG

>NZ_CP011130|2|2|162025-162105|CRISPRCasFinder
CGTCATTCCCGCGAAGGCGGGAATCCAG	AGACTTCAGCGCCATTCCACCAGAA
CGTCATTCCCGCGAAAGCGGGAATCCAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057920352.1|162263_162944_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223620
NZ_CP011130.1|WP_057920350.1|157531_159049_+|glucose-6-phosphate-dehydrogenase	unknown	unknown	gnl|CDD|235579
NZ_CP011130.1|WP_036103539.1|164409_165456_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380487
NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein	unknown	unknown	gnl|CDD|197210
NZ_CP011130.1|WP_057920347.1|151383_151953_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920349.1|154425_155571_-|N-acetylglucosamine-6-phosphate-deacetylase	unknown	unknown	gnl|CDD|224733
NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|224973
NZ_CP011130.1|WP_148650133.1|159032_159788_+|6-phosphogluconolactonase	unknown	unknown	gnl|CDD|238694
NZ_CP011130.1|WP_057920357.1|172723_173926_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_187313397.1|163323_163962_+|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	unknown	unknown	gnl|CDD|235577
NZ_CP011130.1|WP_057920351.1|160075_161908_+|phosphogluconate-dehydratase	unknown	unknown	gnl|CDD|181628
NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein	unknown	unknown	gnl|CDD|225228
NZ_CP011130.1|WP_057920348.1|152114_153569_+|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|238624
NZ_CP011130.1|WP_036103525.1|156630_157383_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein	unknown	unknown	gnl|CDD|349760
NZ_CP011130.1|WP_051546979.1|155584_156595_-|SIS-domain-containing-protein	unknown	unknown	gnl|CDD|225132
NZ_CP011130.1|WP_036103540.1|166216_166411_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_148650131.1|149902_150532_+|macro-domain-containing-protein	unknown	unknown	gnl|CDD|394872
NZ_CP011130.1|WP_148650132.1|150538_151387_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920353.1|165525_165981_-|hotdog-fold-thioesterase	unknown	unknown	gnl|CDD|182337

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057920352.1|162263_162944_+|HAD-family-hydrolase	gnl|CDD|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	8.90569e-43
NZ_CP011130.1|WP_057920350.1|157531_159049_+|glucose-6-phosphate-dehydrogenase	gnl|CDD|235579	PRK05722, PRK05722, glucose-6-phosphate 1-dehydrogenase; Validated.	0
NZ_CP011130.1|WP_036103539.1|164409_165456_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380487	cd01545, PBP1_SalR, ligand-binding domain of DNA transcription repressor SalR, a member of the LacI-GalR family of bacterial transcription regulators. Ligand-binding domain of DNA transcription repressor SalR, a member of the LacI-GalR family of bacterial transcription regulators. The SalR binds to glucose based compound Salicin which is chemically related to aspirin. The ligand-binding of SalR is structurally homologous to the periplasmic sugar-binding domain of ABC-transporters and both domains contain the type 1 periplasmic binding protein-like fold. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the type 1 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	4.42816e-116
NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein	gnl|CDD|197210	cd09111, PLDc_ymdC_like_1, Putative catalytic domain, repeat 1, of Escherichia coli uncharacterized protein ymdC and similar proteins. Putative catalytic domain, repeat 1, of Escherichia coli uncharacterized protein ymdC and similar proteins. In Escherichia coli, there are two genes, f413 (ybhO) and o493 (ymdC), which are homologous to gene cls that encodes the Escherichia coli cardiolipin (CL) synthase. The prototype of this subfamily is an uncharacterized protein ymdC specified by the o493 (ymdC) gene. Although the functional characterization of ymdC and similar proteins remains unknown, members of this subfamily show high sequence homology to bacterial CL synthases, which catalyze the reversible phosphatidyl group transfer between two phosphatidylglycerol molecules to form CL and glycerol. Moreover, ymdC and its similar proteins contain two HKD motifs (H-x-K-x(4)-D, where x represents any amino acid residue) that characteriszes the phospholipase D (PLD) superfamily. The two motifs may be part of the active site and may be involved in phosphatidyl group transfer.	6.23263e-65
NZ_CP011130.1|WP_057920349.1|154425_155571_-|N-acetylglucosamine-6-phosphate-deacetylase	gnl|CDD|224733	COG1820, NagA, N-acetylglucosamine-6-phosphate deacetylase [Carbohydrate transport and metabolism].	4.3392e-163
NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein	gnl|CDD|224973	COG2062, SixA, Phosphohistidine phosphatase SixA [Signal transduction mechanisms].	2.19685e-43
NZ_CP011130.1|WP_148650133.1|159032_159788_+|6-phosphogluconolactonase	gnl|CDD|238694	cd01400, 6PGL, 6PGL: 6-Phosphogluconolactonase (6PGL) subfamily; 6PGL catalyzes the second step of the oxidative phase of the pentose phosphate pathway, the hydrolyzation of 6-phosphoglucono-1,5-lactone (delta form) to 6-phosphogluconate. 6PGL is thought to guard against the accumulation of the delta form of the lactone, which may be toxic through its reaction with endogenous cellular nucleophiles.	6.26843e-65
NZ_CP011130.1|WP_187313397.1|163323_163962_+|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	gnl|CDD|235577	PRK05718, PRK05718, keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase; Provisional.	2.3405e-87
NZ_CP011130.1|WP_057920351.1|160075_161908_+|phosphogluconate-dehydratase	gnl|CDD|181628	PRK09054, PRK09054, phosphogluconate dehydratase; Validated.	0
NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein	gnl|CDD|225228	COG2353, COG2353, Uncharacterized conserved protein [Function unknown].	4.91954e-25
NZ_CP011130.1|WP_057920348.1|152114_153569_+|amidohydrolase-family-protein	gnl|CDD|238624	cd01299, Met_dep_hydrolase_A, Metallo-dependent hydrolases, subgroup A is part of the superfamily of metallo-dependent hydrolases, a large group of proteins that show conservation in their 3-dimensional fold (TIM barrel) and in details of their active site. The vast majority of the members have a conserved metal binding site, involving four histidines and one aspartic acid residue. In the common reaction mechanism, the metal ion (or ions) deprotonate a water molecule for a nucleophilic attack on the substrate. The function of this subgroup is unknown.	3.81761e-35
NZ_CP011130.1|WP_036103525.1|156630_157383_-|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	1.78119e-75
NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein	gnl|CDD|349760	cd02042, ParAB_family, partition proteins ParAB family. ParA and ParB of Caulobacter crescentus belong to a conserved family of bacterial proteins implicated in chromosome segregation. ParB binds to DNA sequences adjacent to the origin of replication and localizes to opposite cell poles shortly following the initiation of DNA replication. ParB regulates the ParA ATPase activity by promoting nucleotide exchange in a fashion reminiscent of the exchange factors of eukaryotic G proteins. ADP-bound ParA binds single-stranded DNA, whereas the ATP-bound form dissociates ParB from its DNA binding sites. Increasing the fraction of ParA-ADP in the cell inhibits cell division, suggesting that this simple nucleotide switch may regulate cytokinesis. ParA shares sequence similarity to a conserved and widespread family of ATPases which includes the repA protein of the repABC operon in Rhizobium etli symbiotic plasmid. This operon is involved in the plasmid replication and partition.	1.86382e-32
NZ_CP011130.1|WP_051546979.1|155584_156595_-|SIS-domain-containing-protein	gnl|CDD|225132	COG2222, AgaS, Predicted phosphosugar isomerases [Cell envelope biogenesis, outer membrane].	6.07141e-109
NZ_CP011130.1|WP_148650131.1|149902_150532_+|macro-domain-containing-protein	gnl|CDD|394872	cd02900, Macro_Appr_pase, macrodomain, Appr-1"-pase family. Macrodomains are found in a variety of proteins with diverse cellular functions, as a stand-alone domain or in combination with other domains like in histone macroH2A and some PARPs (poly ADP-ribose polymerases). Macrodomains can recognize ADP-ribose (ADPr) in both its free and protein-linked forms, in related ligands, such as O-acyl-ADP-ribose (OAADPr), and even in ligands unrelated to ADPr. The yeast protein Ymx7 and related proteins in this family contain a stand-alone macrodomain and may be specific phosphatases catalyzing the conversion of ADP-ribose-1"-monophosphate (Appr-1"-p) to ADP-ribose. Appr-1"-p is an intermediate in a metabolic pathway involved in pre-tRNA splicing.	9.88379e-51
NZ_CP011130.1|WP_057920353.1|165525_165981_-|hotdog-fold-thioesterase	gnl|CDD|182337	PRK10254, PRK10254, proofreading thioesterase EntH.	3.87715e-45

Protein sequences

>NZ_CP011130.1|WP_057920351.1|160075_161908_+|phosphogluconate-dehydratase
MNTPLHPVVAQVTHRIQERSRARRTAYLARIDAAGSGGPHRRRLSCGNLAHGFAACSSGDKAALRSGYAPNLGIVTSFNDMLSAHQPLERYPDLLKAAARDCGATAQVAGGVPAMCDGVTQGREGMELSLFSRDVIAMSTAIALSHDMFDAGLYLGVCDKIVPGLLIGALHFGHLPGIFVPAGPMTSGLPNDEKSRVRQRYATGDATRDELLEAEARSYHGPGTCTFYGTANSNQMLMELMGLHLPGSSFVHPNTPLRDALTALAAQRAAQITALGDDYRPIGRIVDEKAIVNGVIGLHATGGSTNHLLHLIAMAAAAGIDLRLEDFDALSSAIPLLARVYPNGSADVNHFHAAGGLAYLIGELLDHGLLHGDVETVAGHGLARYRVEARLGADGQVEYVPSTPTSCDTAVLRPVSEPFRADGGLRVLSGNLGTAAIKVSAVPEDRWVIEAPCRVFVEQQEVKQAFERGELDRDVIVVVRFQGPRANGMPELHQLTPTLTVLQKRGHRVALVTDGRMSGASGQVPAAMHITPEAMAGGPLAKLRDGDVLRLDAIEGTLNVIEPADWDARESVTADLSGHHVGMGRELFAAFRDYAAPADRGAGVFGSVTL
>NZ_CP011130.1|WP_148650133.1|159032_159788_+|6-phosphogluconolactonase
MKMQAERLTVIEPLPLPLHERLFDDGEQLAQALAKQVAADLRGALARHGEASIALSGGNTPKRFFQALSTQTLDWARVTVLPIDERWLPPEHPRSNERLLRENLLQHNAAVARLLPLYRPTETPEMALMPVLTKIANEGLPLDVAVLGMGDDGHVASLFPDLGYDNPALREIGLQPRGRAPVMSVRTAAMPEPRMTLTLSAIFTAPALYLHIEGDKKRAVLDTAQRDPRCSLPIRSVLSGAPSAPTLYWSP
>NZ_CP011130.1|WP_057920350.1|157531_159049_+|glucose-6-phosphate-dehydrogenase
MSVYTVPNTSQAPHLAPLAPFDLVIFGGTGDLALRKLLPALFHRYADGQIVAGTRIVAIARDTQSDADYRGRVREALAKFANLDARESAAIDGFLDLLLYRRLDLSSDGGWPEFAAEFSGDERVRVFYLAVGPDLFGIVGDRLQSHGLVGPKTRVVVEKPLGKDGASANAINDALGRVFNETQIFRIDHYLGKETVQNLTALRFGNALFEPLWKAEHIDHVQITVAETVGVESRAPYYDKSGALRDMVQNHLLQLLCLVAMEPPSSLAADAIRDEKLKVLRALRPIVNGNAAQSTVRGQYKAGAVDGAAVPGYAQELGAQSLTETFVAIKAEVKNWRWAGVPFYLRTGKRLGERVSEIVVTFRQVPHSIFEELTEQDPSSRLAPNKLVLRLQPDEGVKLWLMNKVPGPGGLRLRHVPLDMSFAAAFGGRQADAYERLLMDVVRGNPMLFMRRDEVDAAWKWIDPIRAAWAASADAPRPYTAGSWGPSAAVALIERDGRTWHEDAG
>NZ_CP011130.1|WP_036103525.1|156630_157383_-|GntR-family-transcriptional-regulator
MQSYLQSEFRRQTDARRAPAYQHLRRTLQHAIDNGELTAGQALPGERELGKLLDLSRVTVRKAIAGLVADGLLVQRQGAGTFVAERIVKSFSRLTSFTDDLRARGLDPRSTFLERGVGEVTPEEAMALNLSPGAAVIRYYRLRTADGVALALERTVVPLAVLPDPALVENSLYEAFAKLDIRPARALQRLRAIAFDAEQARLMNLPEGAPGLFIERRTFLDDGRVVEFTRSFYRGDAYDFVAELQSEPTP
>NZ_CP011130.1|WP_051546979.1|155584_156595_-|SIS-domain-containing-protein
MYAEAHEAGDAVARQFAANADSVDDLAQRLQKQPPRFIVTCARGSSDHAATYGKYLFETQLGLVTASASPSVGSVYAIRPKLEGALFVAISQSGKSPDLLRNAEIAKAAGAYVVALVNVIDSPLAQLADTVLGLHAGPETSVAATKSYLCSLAALLQLTARWSNDAALFNAVHALPDALREASKQDWSPLVEGLTDARNLFVIGRGLGLGAAQEAALKFKETCGLHAEAFSSAEVKHGPMAIVGPGFPVLAFAQDDGTGDGTVAVAREFRARGAPVWLAAPGIHGGDALPLARSSHPAMTPLITVASFYQAVNALAVARGYNPDLPPHLNKVTETV
>NZ_CP011130.1|WP_057920349.1|154425_155571_-|N-acetylglucosamine-6-phosphate-deacetylase
MSVTAGALAFVNGRVLSERGFESDLSVIVEDGHIVAVLPGPAPSGTETVDLRGQYLVPGFIDTQVNGGGDVLFNDAPDVDGLRRIAQAHRRFGTTGMLPTLISDDVSVMLRAIDAVREAIAQNVPGILGIHLEGPYLAAARKGVHNPDKFHTPSEAELDQIASLEVGKTLLTLAPERFDNATLQALAARGVVLSAGHTAADYDRLRDAFAHGVSGVTHLFNAMTPLGSREPGGVGACIEDPNAWCGVIVDGEHVHDASLRIAIAAKPRGKILLVTDAMPPVGGEQEDFVLYGQTMTCRNGKCTTADGTLAGSALDMATAVRNTVQRLGLPLDEACRMASAYPADFIGLGHELGRIAPGYRADLVALDDGLRVTDSWIGGLR
>NZ_CP011130.1|WP_057920348.1|152114_153569_+|amidohydrolase-family-protein
MNLSRSIVFALSLCLSVAAVAAEPPKPVAAPAAAKAPAKSPFLAYEQSLLAFTHADVVDGTGAPIRRDQTLLIENGKIRALGASGRIAIPKGATVIDARGKTLLPGLVMMHEHMFYPTGHGNYSEMVHSFPALYLAGGVTTLRTAGAMLPYADLNMRAQIAAGAIAGPDMDVTAPLLNGPGLAVLAVKVVNGADDAERAVSYWADEGVDSYKAYMHIRRDELQGIIEVAHRRSRKVTAHLCSVTFAEASAMGIDNLEHGFAFASDFVTDKQADACPAAITRSLADLDVDSPRMRALIDLLVARKVALTSTLPVFETLVAQRPKVPEAALSLLLPEVREQYEAGWAAMQAKPADWEWARLFPKLGQWEKRFVDAGGLLLAGTDPTGYGGVIPGYASKRQIQLMVEAGFSFEQAVRVASLNGARYLGRDASIGSLEVGKRADVVMIDGDPTRDAGAIERMPLVFKEGKGYRTDAIFEAMKGKVGLH
>NZ_CP011130.1|WP_057920347.1|151383_151953_+|hypothetical-protein
MSATTPSNMRAARCGLLAMLLFLCTISAASTSGGDADLPAGWRLPTDKESSDPAREDSRSRYTEVRADFNGDGVEDLGRMLKTRTGGGEALWVRLSQARQGPAWIKLDEIPRSERGSADLIMAIDTVKPGLIAYACFDTAPDCNFGADAQRPKLRLADASLLYFRPESAASLFFWSNKHRKFMRVWLSD
>NZ_CP011130.1|WP_148650132.1|150538_151387_+|hypothetical-protein
MLAADVRIVSLPCVIGSIAIDANRKTRIQRKDAPRVAKNLHCWRCKTLIPMLDEREWALMSPALSKTIEDIQAYRRKTGASLSECPPQTSACHLYARLTGFVETNPNAIWHHRAADCGPFCRHCRRPLRTARASFCAGCGTPAERGSAEDEAPSASWSVEHGVDARVFGASHHQVLAAVSQAIGPLIAQTHDAGDPHTYLCADAHVSVVTLEGAQIGVSVYRSGRWARSADFGRFLAQALSCRVYCDGGDEAPTVSDGYKLLEIEGGQERWAMQVPKSEAQA
>NZ_CP011130.1|WP_148650131.1|149902_150532_+|macro-domain-containing-protein
MRRPPTHARNTIHMHLMLHLRTLDPGMAEAWRTVFSESEATVEVGDILDAPADAILSPANSFGFMDGGIDLLYSRYFGWELQDAVQARIRTEHDGELPVGQAIVVATGHPNFPFLISAPTMRVPMPVDRTTHVYLAFRAALIAIAAHNRDRADTIASLTSPALGAGIGAMPFDRVARQMRAAYADVVLGETDWRNSARGVLAQHAGLMR
>NZ_CP011130.1|WP_057920352.1|162263_162944_+|HAD-family-hydrolase
MPAPARTTFLFDLDGTLVDSVYQHVLAWKQALDADGIPLSVWRIHRKIGMSGGLFTNILLRETGIDITPERIERLHRLHAEAYGRQATQIRPLPGAVELLAYLTANDIPWAIATSGRMETARHNLVALGVDPEQRVVITRDMVKYAKPDPDLFLAAADKLGADIEHSVVVGDSIWDLLAARRARALGVGLLSGGYGQEELERAGAFRVYEDPADLLKHIDEVAARP
>NZ_CP011130.1|WP_187313397.1|163323_163962_+|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase
MQDLQARVAAVLALAPVVPVLVIDDLKDAVPLARALVAGGLPAIEVTLRTPVALDAVRAIAAEVEGAAVGVGSVRRPSDFVDALKAGATFAVSPGSSPGLIAAAREIDLPWLPGAATASEAMALLEHGYTQLKFFPAESIGGASALKALGGPLPELRFCATGGIGANNAHEYLALKNVPCVGGSWVAPAAAVKAGDWAQIEALARAAVGLRG
>NZ_CP011130.1|WP_036103539.1|164409_165456_-|LacI-family-DNA-binding-transcriptional-regulator
MRRPTIKDVAELAQVSLKTVSRVINDESGVRARTRARVHEAIAELEYRPDPSARSLRSAQPYALGVVYDNPNPYYIISVQNGVLAACRETGYGLQIHPCDSSSPLLAADLIDLVQGARLAGLVLAPPMSERKELVAELVAHGIRLVRIVSAAEDPKDGSPCVWVDDRDAAYDITEHLIQLGHQRIGFLWGGKSHLSSWERYKGYAQALADYGIVEDENLVLPGDYSFDDGFRGARRLFALPDRPTAIFGSNDEIAAGVLAAAKSSGMHVPYDLSIAGFEDSPFSKQSWPTLTTARQATEEIARHAAYRLIAELRRDGDQQAEMPANEGFSPILVVRGSTAPPRPLAGA
>NZ_CP011130.1|WP_057920353.1|165525_165981_-|hotdog-fold-thioesterase
MNSSDPAPTAARPLFRGTTTVDDLNRLSRNTAMEPLGIVFTEIGPDYVRGTMPVDARTHQPYGLLHGGASVLLAETLGSSAGNLCCAEGKVCVGIEINANHLRGVRSGTVTGTARPIHVGGSTQVWDIRIEDEAGKLACISRLTLAVVPKI
>NZ_CP011130.1|WP_036103540.1|166216_166411_-|hypothetical-protein
MNTQTANTVTTTTATTAPAAAPTAPVARHMHRQRDFGVGYGNSSGYASNRSYASNWVQPRFRFA
>NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein
MNPVLRGLAALLALTLSACASLSPAQRDRASALAAAARSQQIDCAAADACAQASPLHALGGQALAASTSEQPRHYAVILDRGPDALLARINLIRSATHSLDLQTYIFDEDDAGKLVLDELLAAARRGVRVRLLLDQLAALRHIDTLAALSGVHVNFEVKLYNPVLHRARITYPRYVLAAACCWRRLNQRMHTKLLLADGQVGISGGRNYQDDYYDWDDEYNFRDRDVLVAGPVADVMGTDFEVFWSDRRSVPVERLADVGQRIIDDGVPALPPIEFERPQRAQAMRDAAADNAQIQERLVAHAIQVGAVRYISDTPDKHRENAENNALASDSLRNLITHSREEVMLQTPYLVLSKSAQQLFRGLHDRPDPPRVIVSTNSLAATDAFIAYALSYKYKRRYLREFGFNIYEYKPFPADAPIDIAATGASLPDLGLEGLVERDDRAHPNSVQGGGLAESRRGEGPDRNSVIYRQRYRQPLAREYAAIRYARRRSNEPVPLKRAGVRIGMHAKSMVIDERIGVIGTHNFDPRGDHYNTESAVVIDDPVFARALADSIRRDIAPANSWVIARRDKPPIFSGLEYSIAKISEHLPLFDLWPVRYATSYEFVPGPDCPSPLYRTDPGFRACYKPVGDFPEVNLGVKSLTTRIFTAFGAGLAPIL
>NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein
MAVSPAATAWSPGWRLRHRVAAVATLAWASAVAVAAPPAAAPPHALEQRPGEARSVETFDPEHTRFSFELRTRWGQKVAGQFPRYDGELTVLADGRHQVRIRLAAGAVVVGDSERYTRLARGERFFNAPRYPYIEFLSEPHSPDLARTGGPLRGRLTLHGVSRMETFILAPATCAKPGEDCDGIAHGSVSRDDYGLDGWQLALGDRVRFTMQVRLQSTQSKLAPPKSAVPKPAPSRNPDPVPAKPAER
>NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein
MRELILLRHAHAEPAANGQADLDRPLSAEGLAEAEAAGRWLAENKLIPDCVLCSPSRRTRETLEAVLGAIGYVEQRIEPSIFEATPGTLIALADTHHEAERLMLVGHNPGLERLAALLHSGQSGDYRGMPPGGVAVLTVPAGVSLEPGSAQLSAFWWP
>NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein
MKTVLVASSKGGVGKTTIATHLAAQAALEGLRTALIDADPQGSSTRWAQRRSVLESAVLALDGTRRKAWRKQLPEDTQRVVIDAPAGAMADDLESFLEFADAVVVPIQPSTLDIEATVPFLDSLAQHPRVRRGQLRVGLIGNKLKPWTNASQQAIELLREWPYPVVVQIRDSQAYVVMTALGKSLFDYHSQQIREHQADWQPLLKWLKK
>NZ_CP011130.1|WP_057920357.1|172723_173926_-|hypothetical-protein
MSETKRAGRPRSWLLLLLLAAVCACDRAPGKPAADSDAPTRAAITDAGPVASAPLSDAGSIRGATDDESRARAAASLEQAQSDYLSALRIHLKTLADRGDPHSQLQLALLLPLSQPDSISEQLLAARQRALDKAAAVSGQEGLVAWLQAMDCFEREDCDLQPALSRLQQVEPDNAMAWLLALEDAARSDADPAQLDRYLRLAAQADHYDDHLTDSSRETQKALEQVAMPPMTSQAEAALRKAAKLEGSTHEHDGHALIVAALATPMTFPPYRATFELCKPQAVRAESQRSGDCRAVLTLMADGDSLLAQAMGTSRMVQFAAGGRDDAYWRERLRESYWLRENFARFDSPAMLRAVRELGEVPAARAELERLGESRPPLGWLPESVNGRALITTGRLPPKP

Crispr_ID: NZ_CP011130_3

• CRISPR_ID: NZ_CP011130_3
• CRISPR_location: 178797-178877
• CRISPR_type: Orphan
• Repeat_type: I-E
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_3

Consensus_repeat	Method
CTGGATTCCCGCTTTCGCGGGAATGACG	CRISPRCasFinder

spacers of NZ_CP011130_3

>3.1|178825|25|NZ_CP011130|CRISPRCasFinder
TTCTGGTGAGATGTCGCTGAAGTCT

CRISPR arrays and Neighbor proteins around NZ_CP011130_3

CRISPR arrays

The CRISPR arrays of NZ_CP011130_3

>merge|NZ_CP011130|3|178797-178877|CRISPRCasFinder
CTGGATTCCCGCTTTCGCGGGAATGACGTTCTGGTGAGATGTCGCTGAAGTCTCTGGATTCCCGCCTTCGCGGGAATGACG

>NZ_CP011130|3|3|178797-178877|CRISPRCasFinder
CTGGATTCCCGCTTTCGCGGGAATGACG	TTCTGGTGAGATGTCGCTGAAGTCT
CTGGATTCCCGCCTTCGCGGGAATGACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057920366.1|192487_194905_-|family-20-glycosylhydrolase	unknown	unknown	gnl|CDD|119333
NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein	unknown	unknown	gnl|CDD|349760
NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein	unknown	unknown	gnl|CDD|197210
NZ_CP011130.1|WP_057920365.1|191597_192236_-|tetratricopeptide-repeat-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_187313398.1|176867_177263_-|gamma-glutamylcyclotransferase	unknown	unknown	gnl|CDD|119400
NZ_CP011130.1|WP_036113330.1|186026_186689_+|ankyrin-repeat-domain-containing-protein	unknown	unknown	gnl|CDD|293786
NZ_CP011130.1|WP_057920362.1|183797_185312_+|hypothetical-protein	unknown	unknown	gnl|CDD|238287
NZ_CP011130.1|WP_057923365.1|177335_178223_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920357.1|172723_173926_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|224973
NZ_CP011130.1|WP_057920359.1|175345_176833_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|177094
NZ_CP011130.1|WP_051547947.1|180993_181974_+|DUF2974-domain-containing-protein	unknown	unknown	gnl|CDD|238287
NZ_CP011130.1|WP_057920367.1|195186_197859_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|273804
NZ_CP011130.1|WP_036103540.1|166216_166411_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920358.1|174120_175029_-|AEC-family-transporter	unknown	unknown	gnl|CDD|223751
NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein	unknown	unknown	gnl|CDD|225228
NZ_CP011130.1|WP_052756530.1|182040_182772_+|ankyrin-repeat-domain-containing-protein	unknown	unknown	gnl|CDD|293786
NZ_CP011130.1|WP_057920361.1|179039_180788_-|gamma-glutamyltransferase	unknown	unknown	gnl|CDD|223482
NZ_CP011130.1|WP_057920364.1|187152_190110_-|response-regulator	unknown	unknown	gnl|CDD|237951
NZ_CP011130.1|WP_046659686.1|190116_191313_-|EAL-domain-containing-response-regulator	unknown	unknown	gnl|CDD|238923

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057920366.1|192487_194905_-|family-20-glycosylhydrolase	gnl|CDD|119333	cd06563, GH20_chitobiase-like, The chitobiase of Serratia marcescens is a beta-N-1,4-acetylhexosaminidase with a glycosyl hydrolase family 20 (GH20) domain that hydrolyzes the beta-1,4-glycosidic linkages in oligomers derived from chitin. Chitin is degraded by a two step process: i) a chitinase hydrolyzes the chitin to oligosaccharides and disaccharides such as di-N-acetyl-D-glucosamine and chitobiose, ii) chitobiase then further degrades these oligomers into monomers. This GH20 domain family includes an N-acetylglucosamidase (GlcNAcase A) from Pseudoalteromonas piscicida and an N-acetylhexosaminidase (SpHex) from Streptomyces plicatus. SpHex lacks the C-terminal PKD (polycystic kidney disease I)-like domain found in the chitobiases. 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.	0
NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein	gnl|CDD|349760	cd02042, ParAB_family, partition proteins ParAB family. ParA and ParB of Caulobacter crescentus belong to a conserved family of bacterial proteins implicated in chromosome segregation. ParB binds to DNA sequences adjacent to the origin of replication and localizes to opposite cell poles shortly following the initiation of DNA replication. ParB regulates the ParA ATPase activity by promoting nucleotide exchange in a fashion reminiscent of the exchange factors of eukaryotic G proteins. ADP-bound ParA binds single-stranded DNA, whereas the ATP-bound form dissociates ParB from its DNA binding sites. Increasing the fraction of ParA-ADP in the cell inhibits cell division, suggesting that this simple nucleotide switch may regulate cytokinesis. ParA shares sequence similarity to a conserved and widespread family of ATPases which includes the repA protein of the repABC operon in Rhizobium etli symbiotic plasmid. This operon is involved in the plasmid replication and partition.	1.86382e-32
NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein	gnl|CDD|197210	cd09111, PLDc_ymdC_like_1, Putative catalytic domain, repeat 1, of Escherichia coli uncharacterized protein ymdC and similar proteins. Putative catalytic domain, repeat 1, of Escherichia coli uncharacterized protein ymdC and similar proteins. In Escherichia coli, there are two genes, f413 (ybhO) and o493 (ymdC), which are homologous to gene cls that encodes the Escherichia coli cardiolipin (CL) synthase. The prototype of this subfamily is an uncharacterized protein ymdC specified by the o493 (ymdC) gene. Although the functional characterization of ymdC and similar proteins remains unknown, members of this subfamily show high sequence homology to bacterial CL synthases, which catalyze the reversible phosphatidyl group transfer between two phosphatidylglycerol molecules to form CL and glycerol. Moreover, ymdC and its similar proteins contain two HKD motifs (H-x-K-x(4)-D, where x represents any amino acid residue) that characteriszes the phospholipase D (PLD) superfamily. The two motifs may be part of the active site and may be involved in phosphatidyl group transfer.	6.23263e-65
NZ_CP011130.1|WP_187313398.1|176867_177263_-|gamma-glutamylcyclotransferase	gnl|CDD|119400	cd06661, GGCT_like, GGCT-like domains, also called AIG2-like family. Gamma-glutamyl cyclotransferase (GGCT) catalyzes the formation of pyroglutamic acid (5-oxoproline) from dipeptides containing gamma-glutamyl, and is a dimeric protein. In Homo sapiens, the protein is encoded by the gene C7orf24, and the enzyme participates in the gamma-glutamyl cycle. Hereditary defects in the gamma-glutamyl cycle have been described for some of the genes involved, but not for C7orf24. The synthesis and metabolism of glutathione (L-gamma-glutamyl-L-cysteinylglycine) ties the gamma-glutamyl cycle to numerous cellular processes; glutathione acts as a ubiquitous reducing agent in reductive mechanisms involved in protein and DNA synthesis, transport processes, enzyme activity, and metabolism. AIG2 (avrRpt2-induced gene) is an Arabidopsis protein that exhibits RPS2- and avrRpt2-dependent induction early after infection with Pseudomonas syringae pv maculicola strain ES4326 carrying avrRpt2. avrRpt2 is an avirulence gene that can convert virulent strains of P. syringae to avirulence on Arabidopsis thaliana, soybean, and bean. The family also includes bacterial tellurite-resistance proteins (trgB); tellurium (Te) compounds are used in industrial processes and had been used as antimicrobial agents in the past. Some members have been described proteins involved in cation transport (chaC).	5.42855e-12
NZ_CP011130.1|WP_036113330.1|186026_186689_+|ankyrin-repeat-domain-containing-protein	gnl|CDD|293786	sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.	1.90983e-16
NZ_CP011130.1|WP_057920362.1|183797_185312_+|hypothetical-protein	gnl|CDD|238287	cd00519, Lipase_3, Lipase (class 3). Lipases are esterases that can hydrolyze long-chain acyl-triglycerides into di- and monoglycerides, glycerol, and free fatty acids at a water/lipid interface. A typical feature of lipases is "interfacial activation," the process of becoming active at the lipid/water interface, although several examples of lipases have been identified that do not undergo interfacial activation . The active site of a lipase contains a catalytic triad consisting of Ser - His - Asp/Glu, but unlike most serine proteases, the active site is buried inside the structure. A "lid" or "flap" covers the active site, making it inaccessible to solvent and substrates. The lid opens during the process of interfacial activation, allowing the lipid substrate access to the active site. .	1.28374e-07
NZ_CP011130.1|WP_057920364.1|187152_190110_-|response-regulator	gnl|CDD|237951	PRK15347, PRK15347, two component system sensor kinase.	1.0596e-76
NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein	gnl|CDD|224973	COG2062, SixA, Phosphohistidine phosphatase SixA [Signal transduction mechanisms].	2.19685e-43
NZ_CP011130.1|WP_057920359.1|175345_176833_+|AAA-family-ATPase	gnl|CDD|177094	CHL00195, ycf46, Ycf46; Provisional.	7.21911e-102
NZ_CP011130.1|WP_051547947.1|180993_181974_+|DUF2974-domain-containing-protein	gnl|CDD|238287	cd00519, Lipase_3, Lipase (class 3). Lipases are esterases that can hydrolyze long-chain acyl-triglycerides into di- and monoglycerides, glycerol, and free fatty acids at a water/lipid interface. A typical feature of lipases is "interfacial activation," the process of becoming active at the lipid/water interface, although several examples of lipases have been identified that do not undergo interfacial activation . The active site of a lipase contains a catalytic triad consisting of Ser - His - Asp/Glu, but unlike most serine proteases, the active site is buried inside the structure. A "lid" or "flap" covers the active site, making it inaccessible to solvent and substrates. The lid opens during the process of interfacial activation, allowing the lipid substrate access to the active site. .	8.12833e-07
NZ_CP011130.1|WP_057920358.1|174120_175029_-|AEC-family-transporter	gnl|CDD|223751	COG0679, COG0679, Predicted permeases [General function prediction only].	3.35077e-37
NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein	gnl|CDD|225228	COG2353, COG2353, Uncharacterized conserved protein [Function unknown].	4.91954e-25
NZ_CP011130.1|WP_052756530.1|182040_182772_+|ankyrin-repeat-domain-containing-protein	gnl|CDD|293786	sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.	2.33827e-19
NZ_CP011130.1|WP_057920361.1|179039_180788_-|gamma-glutamyltransferase	gnl|CDD|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP011130.1|WP_046659686.1|190116_191313_-|EAL-domain-containing-response-regulator	gnl|CDD|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	9.41907e-91
NZ_CP011130.1|WP_057920367.1|195186_197859_-|TonB-dependent-receptor	gnl|CDD|273804	TIGR01782, TonB-dependent_receptor, TonB-dependent receptor. This model represents a family of TonB-dependent outer-membrane receptors which are found mainly in Xanthomonas and Caulobacter. These appear to represent the expansion of a paralogous family in that the 22 X. axonopodis (21 in X. campestris) and 18 C. crescentus sequences are more closely related to each other than any of the many TonB-dependent receptors found in other species. In fact, the Crescentus and Xanthomonas sequences are inseparable on a phylogenetic tree using a PAM-weighted neighbor-joining method, indicating that one of the two genuses may have acquired this set of receptors from the other. The mechanism by which this family is shared between Xanthomonas, a gamma proteobacterial plant pathogen and Caulobacter, an alpha proteobacterial aquatic organism is unclear. [Transport and binding proteins, Porins].	3.56306e-174

Protein sequences

>NZ_CP011130.1|WP_057923365.1|177335_178223_-|hypothetical-protein
MSIALVTSQVHPDIDPDDEGLVVALRAHGIEPIACMWNDPSVDWAAFDALLVRSTWDYFQHYTEFLRWYAHIAELGVAIVNPLPLLIWNSDKRYLLELAKLDVPIIATTHARGDELEATLASMSGEVVVKPSVSGGAWHTVRGRIGSGEFDQALAALPRELDYLIQPFMPQIVEQGEWSLLFFGGVYSHAVLKKPGADDYRVQTYFGGTADLTEPGPSILAAARHALQAVTALGYRDQAYVRVDGVVDDGVFRVMELEFIEPFLHFAAHPPAAGLFAAQLARRWQALRAPATLAT
>NZ_CP011130.1|WP_187313398.1|176867_177263_-|gamma-glutamylcyclotransferase
MTPQSDRPDVDQAGAEADHGERLFSYGTLQLPAVQQSTFGRLLHGEADALVGYRRGMVRIEDADVVATSGEAWHPIVEASGDAHDTVAGTVFAISAEELARADAYEVDDYRRVEAELASGRRAWVYVKREA
>NZ_CP011130.1|WP_057920359.1|175345_176833_+|AAA-family-ATPase
MSDLQDLTALIRANTPLIVIETRDESRVVELFRQALMNVWRALYRWSITEGLRRVDLDREEGTDVAPDISTTLQAIRDADQRGIYLLFDAHPYLSYASTQRQLREIAQRRDCEPHVLVLIGHKLELPPDLDSLAVRYTPRLPDANALLKLVREEAENYARENGGRRVEVDGEAVQQIVRNLRGIDPVDARRIARHLIFRDGALNADDLPELAKLKFELLNRSGHLHYEYDSARMSEVAGARRLKRWVEQRRAVFVSGEAPPGLDPPKGILLLGVQGCGKSMIAKAVAAGFGVPLVRLDFGTLYDKFHGETEKNLRAALASAEQLSPAVLWIDEIEKGLAGDGSDADGGVSRRVLGYLLTWMAERKSRLFLVATANQIDALPPELLRKGRFDEIFFVDLPVAEVRGELFATHLRKRGLTPEHFDLNALASASDGFSGAEIEQAIVASMYAALAANTPLSDFQLRAELKQTRPLSVLMAEQVESLREWARTRTVAAD
>NZ_CP011130.1|WP_057920358.1|174120_175029_-|AEC-family-transporter
MAFDAFALVLAMLVLGYLFQRLRVLPDNAAQTLNLVVLYVCLPAAVLRYAPRLHLEPALLGVAAVPWLLLGATVLVVGALSRWLNFRRDEHAVLLLTVALGNTSFLGYPLTRALIGEHALPYAVVYDQFGAFLILSTFGLWVLARYGSDTRPSARDMALRIVKFPPLWALLIGFSVMPANPPSAIAGALQRLSDALLPLAMLTIGLSVKLALPRDELKPLACGLILKLALMPALAWALVPLLGLHGEMARTTVLEAAMPSMVTAGALAIAHQLAPRLAAAMVGYGLLLSLLTLPLWARVAVG
>NZ_CP011130.1|WP_057920357.1|172723_173926_-|hypothetical-protein
MSETKRAGRPRSWLLLLLLAAVCACDRAPGKPAADSDAPTRAAITDAGPVASAPLSDAGSIRGATDDESRARAAASLEQAQSDYLSALRIHLKTLADRGDPHSQLQLALLLPLSQPDSISEQLLAARQRALDKAAAVSGQEGLVAWLQAMDCFEREDCDLQPALSRLQQVEPDNAMAWLLALEDAARSDADPAQLDRYLRLAAQADHYDDHLTDSSRETQKALEQVAMPPMTSQAEAALRKAAKLEGSTHEHDGHALIVAALATPMTFPPYRATFELCKPQAVRAESQRSGDCRAVLTLMADGDSLLAQAMGTSRMVQFAAGGRDDAYWRERLRESYWLRENFARFDSPAMLRAVRELGEVPAARAELERLGESRPPLGWLPESVNGRALITTGRLPPKP
>NZ_CP011130.1|WP_057920356.1|171009_171639_-|ParA-family-protein
MKTVLVASSKGGVGKTTIATHLAAQAALEGLRTALIDADPQGSSTRWAQRRSVLESAVLALDGTRRKAWRKQLPEDTQRVVIDAPAGAMADDLESFLEFADAVVVPIQPSTLDIEATVPFLDSLAQHPRVRRGQLRVGLIGNKLKPWTNASQQAIELLREWPYPVVVQIRDSQAYVVMTALGKSLFDYHSQQIREHQADWQPLLKWLKK
>NZ_CP011130.1|WP_036115859.1|170421_170898_-|histidine-phosphatase-family-protein
MRELILLRHAHAEPAANGQADLDRPLSAEGLAEAEAAGRWLAENKLIPDCVLCSPSRRTRETLEAVLGAIGYVEQRIEPSIFEATPGTLIALADTHHEAERLMLVGHNPGLERLAALLHSGQSGDYRGMPPGGVAVLTVPAGVSLEPGSAQLSAFWWP
>NZ_CP011130.1|WP_187313317.1|169684_170431_-|YceI-family-protein
MAVSPAATAWSPGWRLRHRVAAVATLAWASAVAVAAPPAAAPPHALEQRPGEARSVETFDPEHTRFSFELRTRWGQKVAGQFPRYDGELTVLADGRHQVRIRLAAGAVVVGDSERYTRLARGERFFNAPRYPYIEFLSEPHSPDLARTGGPLRGRLTLHGVSRMETFILAPATCAKPGEDCDGIAHGSVSRDDYGLDGWQLALGDRVRFTMQVRLQSTQSKLAPPKSAVPKPAPSRNPDPVPAKPAER
>NZ_CP011130.1|WP_057920354.1|167698_169672_-|phospholipase-D-family-protein
MNPVLRGLAALLALTLSACASLSPAQRDRASALAAAARSQQIDCAAADACAQASPLHALGGQALAASTSEQPRHYAVILDRGPDALLARINLIRSATHSLDLQTYIFDEDDAGKLVLDELLAAARRGVRVRLLLDQLAALRHIDTLAALSGVHVNFEVKLYNPVLHRARITYPRYVLAAACCWRRLNQRMHTKLLLADGQVGISGGRNYQDDYYDWDDEYNFRDRDVLVAGPVADVMGTDFEVFWSDRRSVPVERLADVGQRIIDDGVPALPPIEFERPQRAQAMRDAAADNAQIQERLVAHAIQVGAVRYISDTPDKHRENAENNALASDSLRNLITHSREEVMLQTPYLVLSKSAQQLFRGLHDRPDPPRVIVSTNSLAATDAFIAYALSYKYKRRYLREFGFNIYEYKPFPADAPIDIAATGASLPDLGLEGLVERDDRAHPNSVQGGGLAESRRGEGPDRNSVIYRQRYRQPLAREYAAIRYARRRSNEPVPLKRAGVRIGMHAKSMVIDERIGVIGTHNFDPRGDHYNTESAVVIDDPVFARALADSIRRDIAPANSWVIARRDKPPIFSGLEYSIAKISEHLPLFDLWPVRYATSYEFVPGPDCPSPLYRTDPGFRACYKPVGDFPEVNLGVKSLTTRIFTAFGAGLAPIL
>NZ_CP011130.1|WP_036103540.1|166216_166411_-|hypothetical-protein
MNTQTANTVTTTTATTAPAAAPTAPVARHMHRQRDFGVGYGNSSGYASNRSYASNWVQPRFRFA
>NZ_CP011130.1|WP_057920361.1|179039_180788_-|gamma-glutamyltransferase
MPPSTHAPRRALRPCLHAVLALACALALPSAANAADRISGQAFATRSEVYAPHAIAATSHPLATQIALDVMKGGGSAVDAAIAANAALGLMEPTGNGVGGDLFAIVWDPKTKKLYGYNGSGRSPKSLTLAEFQKRGLKEIPPTGPLPVTVPGTVDGWFALHERFGRKPIADDLAPAIRYAREGHPVHEVIAYYWNASVPRLSKWPGFKEQFTVDGRAPRVGEMWKNPNLANTLEQIAKGGRDAFYKGDIARTIDAYFKANGGYLSYDDLASHHGEWVEPVSSNYRGYDLWELPPNGQGIAALQILNILEAYDLKSYGFGSVEHVHLFTEAKKLAFADRARWYADPAFEKSSPVAKLISKDYAKQRRKLISMDKALKEVQPATPAQLDQGDTIYMTVADADGMMVSLIQSNYRGMGSGMAAPGLGFIFQDRGEQFVLKEGHPNSFAPGKRPFHTIIPAFVTKAGKPWLSFGVMGGGMQPQGHAQIMMNLIDFGMNLQEAGDAPRIQHDGSTEPAGQAEVMSDGGELDLETGYPYETIRELMRRGHSVRFAHGPYGGYQAIMVNPNGGYIGASESRKDGQAAGY
>NZ_CP011130.1|WP_051547947.1|180993_181974_+|DUF2974-domain-containing-protein
MSVQLQPSQLQPNWQNPSEALPPAAQPVALAQPEAGPYTLEASYHPQLLGVNAQQRPAANAAPDPTSFDQQLRGQDAQAIDLQMAQIAEAVYNPATTSVAGWNRLDDAQLSAAGIDPASLENSDTGFRAGIFTDGNGKYVVAYAGSNDVQDWINNARQGIGWDSKQYDQAVQLARDAQEAFGENMVITGHSLGGGLAATAALATDTAAVTFNASGVHDDTLRGLGLDPGTVKDDAQNGQIRRYNVGGEILTAAQEDVPLLNGIPDAPGHEITLDDPHPPQAPDFTWNPIEMARRTAEYVADKATRPGELHAIGPLIEAMQTQQPWN
>NZ_CP011130.1|WP_052756530.1|182040_182772_+|ankyrin-repeat-domain-containing-protein
MRAATLPALTICLALAGAACSGDAMDAKQAFPDPRSAELAQAAADGDAARVRALVAAGADPNARGARELTQLQYAMLAQSPRGLQALLDNGADPARPGLGGSTAVHGAAIANDPQYLDILLAHRADPNAAHAETGETPLSEAAAPRYQAQFDALLRAGADPDRADRMGNTPLHQAAKLNASGQVLALLKAGANPNARNQRGASFQTFLFKLPDDKLNPQARAEREAVVAWLKAHDIAVEDAAR
>NZ_CP011130.1|WP_057920362.1|183797_185312_+|hypothetical-protein
MSWSDFTNPVLRFAQLPSVIDNLLHAQPQPVVPPPQVVAPPVTLAAPVELPYSPHVPVPAQVKPEQPFSEQLAGQQPQKEIDTALAELSSDVYETTNTGAAGWTRLTDDQLTNLKGPDGKPAGIDPASLDVDGSGFRAAVYANGDGQYVVAFAGTNGFNPLGDGDIANDVGQGLGFNTSQYKQAVALAKEAEAAFGDNVVFTGHSLGGGLASTAALATGNTAVTFNAAGLSNDTLRDLGFTPHEARSQAEDGQIRRYNVDGDPLTGAQQGVELINGMPDAVGYELNLAHPGGWANPATAHGTDTVIEAMKTQTPTPTPSIEGDELGLLDNAAETVSETGMDLLGDGLQEVVDLGVDAFNVGYDFGGDLVNVVNNEYANGRYLDGTFKLAGDVTEGALNLTGDVVDGAFNLAGDTLQGAGELTGGLIRDVGEYVGLEGASDTVAGWVENSGEWLGARTDDLGNLAETAIDGLGTAAEATLDFAGDVTEGAVNVAKDVGSFLNPFD
>NZ_CP011130.1|WP_036113330.1|186026_186689_+|ankyrin-repeat-domain-containing-protein
MQASEAFTDVRTAELAQAAADGDAARVRELAAAGANPNERGAKGVTPLQWALYHHSTDGMKALLAAGADPAQGSDDGMTVVHLAAMADHPRYLRVLLDHGVSPDTPNTVTQATPLAAALMGERADNFEALLKAGAKPDLPDRMGNTPLHQAAKVNEFGHALELLRAGASPNTRNVQGASFQRFMFMTPEKILNAQTRRDREAVIEWLREHQIPIEDAQAK
>NZ_CP011130.1|WP_057920364.1|187152_190110_-|response-regulator
MFAWLDRFSIRRQLWGLFALFLLAGTSVLVIDEIEQQRARRTLQTLQDDALLGLRLIKTISDGYGLDVVDTTFRVRNDLVGWDEGLARVEGAQRRIDQAWLRLQTLPHSARETEQLHAAALARRTADAAAAELRAILRRRDLPALGRFADTRLYPAIDPLTQRLQILSDLELTQTDAVVRADLVRSEQVSLLRLIVSVLALGLAALIGRRVLRNASRGIDRLTWLARRMRDHDYTAEPGELPSGELGAVMQAFIDMRRDVLGFETELTGQLIRNERTRAELERRERFQASLLDSAQTAILAVDGDGRFTLVNPFAERLLGVREADLVGRESLQAVFEPRALKTLAAELSGQLEQPVFADWTALRELARSHAAPRETRLRHRNGTWVPALLAVSLTREGEDDAPGLLVVAADLSALKRLERALRASEARAQDANRAKSSFLAAMSHEIRTPMIGVTGMIEVLSHSRLDPEQRHALEVIQHSSQSLLQIIGDILDFSKIEAGRLELATDAVNLPALLRTTVAGFLGAASSRGVQLSCHIDPRIAPAHHADALRLRQIVGNFLSNAVKFTERGVIQVALEYEGRELTNLDTDAADADSTATDSSDSASAAAGHPASGATPPPARDLLCLRVTDTGIGISAEQQQRLFEPFNQADGDTTRRYGGTGLGLAICKRLAELMGGQISLHSEPGIGTTLRLRVALARASQAELDAAPAALPASLALVPRPLPDLATAERERSLILLIDDHPTNRLVIARQLALAGYACEAVASGEEGLQRWRSGRYALLLSDVHMPGLDGYGLARALREEEARAGIGLGDPRRTPLLALTASALKGEAEACLAAGMDDCLIKPIAVARLAASLRQWLPHTAPSEPPPPSLLEGHDRMRVLDVEVLRRLLDDSDSEAGDVLDDFLTATAQDLADLHRAHRDGDLSVLQHAAHRIRGAAQLIGAIELSEAADALEQAARAQDWNLALPLLSDVETAVERLRRLPR
>NZ_CP011130.1|WP_046659686.1|190116_191313_-|EAL-domain-containing-response-regulator
MSISALSVLVVEDHGFQRRMALRLLSELGVARAFEAADGASALRLLEAMTQPPDVVMVDLDMPGMDGIEFIDHLAQRHLARAVLVVSALDAALLHTVQTMARACGLRVLDAVAKPLTKAKLATALGSLRETTADVEEDSPGEITTEAVRAALAGGDIVPWFQPQVELSNGRVIGVEALARWRRGDGRVILPQHFVPVLERDHLLDELTERMLAQACRWKRDWDRAGLRLKLSVNVSASTLDDTGAADRYQRIVREAGVDPAEIVLELTESSLMADAARGLAVLARLRLKGFGLSIDDFGTGWSSLSQLSQVPFTELKIDQEFVAGASQQPRKRAVVEASLDLARKLGLDAVAEGVETIEDWQMLAELGCTTAQGRLIGDAVPGEELPAMLSRWRRPEH
>NZ_CP011130.1|WP_057920365.1|191597_192236_-|tetratricopeptide-repeat-protein
MFTRKLLLATALAAALFAGAAGAQTLPKPNEFYFDADAQTTKPVIAVRETGDAATDRLAKILERKAHAPNEAAQLAHLAMQAGRNDLGRQLYGRALREVDGGSTFWRAINWNYAWDQFRAGAPEDAFRLWATIHNARTVNASWMPPTYALVLWTLGRKDEAVQWYAAAVRTEPDQWRTSARYAELLPEWRDSERATLAEVQQAWAAKPPKWP
>NZ_CP011130.1|WP_057920366.1|192487_194905_-|family-20-glycosylhydrolase
MKTRTTRSLLAAAALAAALTACHSAAPREAAAHVQAAHDGEAASAARDTDTVAAHRTAIIPRPLKTQAQRGQFEFGANTPVQVHAGHAGERRVADYFAAKVRALRGFAPSIAETQTESKNARDAIALSLEPDLAIGEEAYVLDIQSDGVRIRARTEAGLFYGAVSLWQLLTADGGQGATRIAAQRIEDAPAYRWRGVMLDVARHFRGVDEVKSVIDQMALHKLNTFHWHLTDDQGWRIEIKQYPRLTQVGGCRIPAGANGRDAQGKPQPYCGYYTQEQIRDVVAYAAARHITVVPEIEMPGHAQAAIAAYPNLGVTDVVRKAPRVSPDWGVHTYLFGVDDSTFDFLENVLDEVAGLFPSKYIHIGGDEAAKDQWIASKKVQARIKSLGLKDEMALQSWFVGRIGQHLQTHDRILLGWDEILEGGRLPANATVMSWRGTAGAVEAAREGHDVIVAPDRQLYLDYVQSDRDDEPPGRFPASTLRDFYDFSIVPAELTAQQSKHVIGAQANLWSEHRRSFDRIQTTLYPRLDALAEVVWSPPSSRDWNDFQQRLAPQLARYRAQDVLVSDVAYAVSFKVIDGADGQPQLSLSNQAGFGEIRYRSDGGEPDPASPRYRQPLPATPPLDLVATPFFDGRPLAAPRRFSARDLAGLSRRTSAGLRPCREGYNLRLEDDAARDGGRDGERAALTVNLIDPCWIYPAAALDGVGAIEVQVGQLPYNFQLWHDTDKIVTRKAVQGGALEVRLDDCKSAPIARLPLAAAKRSDGITTLRARLPAHSGRHDLCFVFASGAHDPLWALDAVTLHPPE
>NZ_CP011130.1|WP_057920367.1|195186_197859_-|TonB-dependent-receptor
MKARKTILSASIVTALLMGPGLAFAQDAAPAAASQATDLDTVVVTGIRASLEKSLDTKRANVTVSEAITAEDIGKFASTNVAEAMSQIPGVTLDRRFGQGERVSIDGTDPSLNLSFLDGHPVAQAIWLYGEQPNRGFDYTLLAPEILGRLEIIKSSEARITEGSLGGTVLMHTRKPLDLDANSVAGSVSYNYSDQGSKGRPSASVLYSWKNPQENFGVSVAAQHYEEQVDRQGLEIFGYAKASTFTNAARAGLDPNAEVPNSINAAWFQQHRKRDSAVVNLQFQPNDQWNIDLQGLYIKENFDNYNQSLYSFLTWNDGTVGAVNQLGDAKNGVVTSGHSNANADPLGGTVIYDNNVRESEVVTKGIDLRTSFKGEGWGFKGQIGSSKSENENLAQYFIEPVYNGGFSWDINRGIKFDNPDAARNPANWGPAGGVANGWMGNNGVFSTESKDTYGQVDFNVEFDSAINNLQFGVRRAKHEESFDLNIYGPVNRGTLADVGTIGLTDIRGFTGDHGRHIQVGRGNVLDWVKGSPLDFNNPDAAGYLNNSWALEQTNTAAYVQADFSAGAWRGNFGVRYVESKTDASGFVYGGAPSLTDLASKWQTKSRKEDFFLPSFNVVYDTGNDVLLRFAAAKVIAWAPYNQMVNNTFLNDTTYTGSGGNAELSPYESTNFNLSAEWYFAEQSVLAASVFYKDIDNYIDSAARIERQYNSIRDTNRVVFDTTLVGFHGCTADGYCDYDIQRPRNAGKGKVKGFNVSYQQPFADTGFGMTANYTYADGENNTGDPLPYQSRDSVAISPYYEKGPLSVRLSYNWRSHYLAGGYVAGAAPASVDDYSELGASVGWKFNDNMGLSFDAMNILDEEYVQYSGNQDKPVGKYHSGRRYMAAFRFNF

Crispr_ID: NZ_CP011130_4

• CRISPR_ID: NZ_CP011130_4
• CRISPR_location: 513649-513949
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP011130_4

Consensus_repeat	Method
CGANGNNGATGCTGCCGTTGACNGT	CRT

spacers of NZ_CP011130_4

>4.1|513674|32|NZ_CP011130|CRT
TTCCAGGTCGCCGCGCACGGTGCCGCCGCGAT
>4.2|513731|32|NZ_CP011130|CRT
TTCGATGCCGCCGTTCGCGGTCAGGTTGGTGC
>4.3|513788|29|NZ_CP011130|CRT
TTCCAGGCCGCCGGTCTGGCTGCTGTTGC
>4.4|513842|29|NZ_CP011130|CRT
CTCGGCCTTGCCGACGCGGGCGCTGTCGC
>4.5|513896|29|NZ_CP011130|CRT
GTCCAGGTCGCCCTGGCGCTGGCTGGCTT

CRISPR arrays and Neighbor proteins around NZ_CP011130_4

CRISPR arrays

The CRISPR arrays of NZ_CP011130_4

>merge|NZ_CP011130|4|513649-513949|CRT
CCAGGCCGATCGCGCCGTTGACGGTTTCCAGGTCGCCGCGCACGGTGCCGCCGCGATCGACGAAGATGCTGCCGTTGACGGTTTCGATGCCGCCGTTCGCGGTCAGGTTGGTGCCGGCGCGGATGCTGCCGTTGACCGTTTCCAGGCCGCCGGTCTGGCTGCTGTTGCCGACGTTGATGCTGCCGTTGACCGTCTCGGCCTTGCCGACGCGGGCGCTGTCGCCGATCTTGATGCTGCCGTTGACGGTGTCCAGGTCGCCCTGGCGCTGGCTGGCTTCGACGTTGATGCTGCCGTTGACCTT

>NZ_CP011130|4|1|513649-513949|CRT
CCAGGCCGATCGCGCCGTTGACGGT	TTCCAGGTCGCCGCGCACGGTGCCGCCGCGAT
CGACGAAGATGCTGCCGTTGACGGT	TTCGATGCCGCCGTTCGCGGTCAGGTTGGTGC
CGGCGCGGATGCTGCCGTTGACCGT	TTCCAGGCCGCCGGTCTGGCTGCTGTTGC
CGACGTTGATGCTGCCGTTGACCGT	CTCGGCCTTGCCGACGCGGGCGCTGTCGC
CGATCTTGATGCTGCCGTTGACGGT	GTCCAGGTCGCCCTGGCGCTGGCTGGCTT
CGACGTTGATGCTGCCGTTGACCTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_082648256.1|524012_525470_-|adenylosuccinate-lyase-family-protein	unknown	unknown	gnl|CDD|176469
NZ_CP011130.1|WP_057923390.1|511408_513154_-|M28-family-peptidase	unknown	unknown	gnl|CDD|349910
NZ_CP011130.1|WP_057920506.1|508772_509888_-|DJ-1/PfpI-family-protein	unknown	unknown	gnl|CDD|153235
NZ_CP011130.1|WP_036112535.1|520435_521131_-|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|223777
NZ_CP011130.1|WP_057920509.1|514273_515809_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	unknown	unknown	gnl|CDD|235463
NZ_CP011130.1|WP_082648254.1|510809_511265_-|MAPEG-family-protein	unknown	unknown	gnl|CDD|226211
NZ_CP011130.1|WP_057920511.1|519296_519938_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046659767.1|521396_522764_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|367457
NZ_CP011130.1|WP_036112538.1|519979_520297_-|DUF1820-family-protein	unknown	unknown	gnl|CDD|226900
NZ_CP011130.1|WP_082648255.1|517462_518992_+|S41-family-peptidase	unknown	unknown	gnl|CDD|223864
NZ_CP011130.1|WP_057920507.1|509979_510714_-|2OG-Fe-dioxygenase-family-protein	unknown	unknown	gnl|CDD|370779
NZ_CP011130.1|WP_148650159.1|505962_506211_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_051547931.1|494456_495938_-|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_CP011130.1|WP_057923389.1|496142_497357_+|tyrosine--tRNA-ligase	unknown	unknown	gnl|CDD|235645
NZ_CP011130.1|WP_057920513.1|525528_526899_-|adenylosuccinate-lyase	unknown	unknown	gnl|CDD|176469
NZ_CP011130.1|WP_057920505.1|508079_508766_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP011130.1|WP_148650158.1|504200_505844_+|hypothetical-protein	unknown	unknown	gnl|CDD|215426
NZ_CP011130.1|WP_082648253.1|506766_508083_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP011130.1|WP_057920510.1|515808_517077_+|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|227278
NZ_CP011130.1|WP_057920512.1|522852_523926_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|316372

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057923390.1|511408_513154_-|M28-family-peptidase	gnl|CDD|349910	cd05660, M28_like_PA, M28 Zn-peptidase containing a protease-associated (PA) domain insert. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions. This subfamily is composed of uncharacterized proteins containing a protease-associated (PA) domain insert which may participate in substrate binding and/or promote conformational changes, influencing the stability and accessibility of the site to substrate.	3.25383e-108
NZ_CP011130.1|WP_057920506.1|508772_509888_-|DJ-1/PfpI-family-protein	gnl|CDD|153235	cd03141, GATase1_Hsp31_like, Type 1 glutamine amidotransferase (GATase1)-like domain found in proteins similar to Escherichia coli Hsp31 protein. Type 1 glutamine amidotransferase (GATase1)-like domain found in proteins similar to Escherichia coli Hsp31 protein (EcHsp31). This group includes EcHsp31 and Saccharomyces cerevisiae Ydr533c protein. EcHsp31 has chaperone activity. Ydr533c is upregulated in response to various stress conditions along with the heat shock family. EcHsp31 coordinates a metal ion using a 2-His-1-carboxylate motif present in various ions that use iron as a cofactor such as Carboxypeptidase A. The catalytic triad typical of GATase1 domains is not conserved in this GATase1-like domain. However, in common with a typical GATase1 domain, a reactive Cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow. For EcHsp31, this Cys together with a different His and, an Asp (rather than a Glu) residue form a different catalytic triad from the typical GATase1 domain. For Ydr533c a catalytic triad forms from the conserved Cys together with a different His and Glu from that of the typical GATase1domain. Ydr533c protein and EcHsp31 are homodimers.	2.0462e-76
NZ_CP011130.1|WP_036112535.1|520435_521131_-|rhomboid-family-intramembrane-serine-protease	gnl|CDD|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	1.98318e-24
NZ_CP011130.1|WP_057920509.1|514273_515809_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	gnl|CDD|235463	PRK05434, PRK05434, 2,3-bisphosphoglycerate-independent phosphoglycerate mutase.	0
NZ_CP011130.1|WP_082648254.1|510809_511265_-|MAPEG-family-protein	gnl|CDD|226211	COG3686, COG3686, Predicted membrane protein [Function unknown].	4.74448e-27
NZ_CP011130.1|WP_036112538.1|519979_520297_-|DUF1820-family-protein	gnl|CDD|226900	COG4517, COG4517, Uncharacterized protein conserved in bacteria [Function unknown].	2.05253e-48
NZ_CP011130.1|WP_046659767.1|521396_522764_+|TonB-dependent-receptor	gnl|CDD|367457	pfam03349, Toluene_X, Outer membrane protein transport protein (OMPP1/FadL/TodX). This family includes TodX from Pseudomonas putida F1 and TbuX from Ralstonia pickettii PKO1. These are membrane proteins of uncertain function that are involved in toluene catabolism. Related proteins involved in the degradation of similar aromatic hydrocarbons are also in this family, such as CymD. This family also includes FadL involved in translocation of long-chain fatty acids across the outer membrane. It is also a receptor for the bacteriophage T2.	2.66829e-105
NZ_CP011130.1|WP_082648256.1|524012_525470_-|adenylosuccinate-lyase-family-protein	gnl|CDD|176469	cd01597, pCLME, prokaryotic 3-carboxy-cis,cis-muconate cycloisomerase (CMLE)_like. This subgroup contains pCLME and related proteins, and belongs to the Lyase class I family. Members of this family for the most part catalyze similar beta-elimination reactions in which a C-N or C-O bond is cleaved with the release of fumarate as one of the products. These proteins are active as tetramers. The four active sites of the homotetrameric enzyme are each formed by residues from three different subunits. CMLE catalyzes the cyclization of 3-carboxy-cis,cis-muconate (3CM) to 4-carboxy-muconolactone in the beta-ketoadipate pathway. This pathway is responsible for the catabolism of a variety of aromatic compounds into intermediates of the citric cycle in prokaryotic and eukaryotic micro-organisms.	5.9009e-176
NZ_CP011130.1|WP_082648255.1|517462_518992_+|S41-family-peptidase	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	5.68557e-123
NZ_CP011130.1|WP_057920507.1|509979_510714_-|2OG-Fe-dioxygenase-family-protein	gnl|CDD|370779	pfam10014, 2OG-Fe_Oxy_2, 2OG-Fe dioxygenase. This family contains 2-oxoglutarate (2OG) and Fe-dependent dioxygenases. It includes L-isoleucine dioxygenase (IDO).	3.58154e-84
NZ_CP011130.1|WP_051547931.1|494456_495938_-|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	1.63335e-46
NZ_CP011130.1|WP_057923389.1|496142_497357_+|tyrosine--tRNA-ligase	gnl|CDD|235645	PRK05912, PRK05912, tyrosyl-tRNA synthetase; Validated.	0
NZ_CP011130.1|WP_057920513.1|525528_526899_-|adenylosuccinate-lyase	gnl|CDD|176469	cd01597, pCLME, prokaryotic 3-carboxy-cis,cis-muconate cycloisomerase (CMLE)_like. This subgroup contains pCLME and related proteins, and belongs to the Lyase class I family. Members of this family for the most part catalyze similar beta-elimination reactions in which a C-N or C-O bond is cleaved with the release of fumarate as one of the products. These proteins are active as tetramers. The four active sites of the homotetrameric enzyme are each formed by residues from three different subunits. CMLE catalyzes the cyclization of 3-carboxy-cis,cis-muconate (3CM) to 4-carboxy-muconolactone in the beta-ketoadipate pathway. This pathway is responsible for the catabolism of a variety of aromatic compounds into intermediates of the citric cycle in prokaryotic and eukaryotic micro-organisms.	0
NZ_CP011130.1|WP_057920505.1|508079_508766_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.63282e-63
NZ_CP011130.1|WP_148650158.1|504200_505844_+|hypothetical-protein	gnl|CDD|215426	PLN02793, PLN02793, Probable polygalacturonase.	7.19089e-06
NZ_CP011130.1|WP_082648253.1|506766_508083_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.05879e-33
NZ_CP011130.1|WP_057920510.1|515808_517077_+|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|227278	COG4942, COG4942, Membrane-bound metallopeptidase [Cell division and chromosome partitioning].	5.0921e-87
NZ_CP011130.1|WP_057920512.1|522852_523926_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|316372	pfam13847, Methyltransf_31, Methyltransferase domain. This family appears to have methyltransferase activity.	1.44845e-17

Protein sequences

>NZ_CP011130.1|WP_057923390.1|511408_513154_-|M28-family-peptidase
MLTATSLVAAALVLSACDKTASKPDAGANAATPAPAQPAGEHGFDGAINAADFAQHVKILASDEFEGRAPGSAGEEKTVQYLQAQFQRMGLKPGNGDSYFQTVPMVETTADETTSLTLQVKGQPRELKFGTDMVVGTRTGQPEVKVDGSDLVFVGYGVNAPEQQWNDYAGVDVKGKTVVMFVNDPGFHGQDATLFEGKRMTYYGRWTYKFEEAARQGAKAALIIHDTAGASYGWDVVKNSWSGAQFDLPAKDDPEPRLPVQGWISNDVARKLLGDLGQNLDQLYQAAGKRGFKAIPLQAKASVDLKSKISEKSSRNVVARLDGAKRPDEAIVYMAHWDHLGNHTGEGGHEGHGADAKTTGPDTIYNGAVDNASGVAGILEIAEAFSKQTPPPDRSLLFLAVTLEESGLLGSKYYVAHPTVPLNKTVAVINLDAMPIIGKARDMTVVGYGSSELEDILKTIADGQQRVLHAEATPQDGFYFRSDHFNFAKAGVPALYAKGGDDLIDGGVEAGKKAQIDYRDNRYHKPADEFDAAWKLDGLVQDLDALYGVGKVLAGNEQWPNWYEGNAFRAAHDTLMAPPAK
>NZ_CP011130.1|WP_082648254.1|510809_511265_-|MAPEG-family-protein
MSIAYWCVLIAALLPYLWVAVAKASGKRYDNRDPRGWQTRQDNPRCNAAYAAHLNAFEAFAPFAAGVVGAQITGVATDWIVGLAMAFIVFRVLHGVFYVTRQPRLRSLAWVLGFGCVLALLVLAALAASENASAQVVLRLLDGSTQAGLPS
>NZ_CP011130.1|WP_057920507.1|509979_510714_-|2OG-Fe-dioxygenase-family-protein
MSPAPRTDHDNFAQSLRGDGFCFVDGETMRGHLLQHGSLQDWPAFADSWNDLAPDQYLASVGRHRRRRHAVFRAGRDGAIERQPHQPHYQSLNYNTLQGDIERWFEPVHDAIAGGASLTTVLGFCRDFFSTLAPQTQAWHIELHQFRIEAHSDEDGQPTPEGVHRDGVDYVLVLLIDRHNILSGTTTIHTADGTELGSFTLTAPLDAALVDDARVFHGVTAVTPQDPQREAHRDVLVVTFRKTA
>NZ_CP011130.1|WP_057920506.1|508772_509888_-|DJ-1/PfpI-family-protein
MTPHRIRRAVLALSLLLAAVPAMAADKILIVVSGEGRDQGKTRPGFEMDEFAQAYLIFRDNGYAIDVASPNGGRVEADKYDATEAFNASLLADAGATGLLAATRKTGELKAADYAAVYVVGGKGAMFDLPADPALRRVVADIYERGGVVAAVCHGPAALVDVRLGNGAWLVDGKRMTGFSNEEEAVFGKRWAKQYRFQLEDALKARGAQWQEAALMMPKLVVDGRLITGQNPYSTPAVAEAIVSALGRQPKARMPWRDERTMTLVQRALNGESAAVRQALAEDRDTYHVQLIGLLGYYQAQATQDLAATRDALAIMQLAAPYMPEPQLRLGMAEAHLRLGDRERARSLTGEVLESHPDMAEAKQLLQRIGS
>NZ_CP011130.1|WP_057920505.1|508079_508766_-|response-regulator-transcription-factor
MVERLRILVVEDHLPLRTAMAAMFEAHGHRADFAADGRTGLRLALDDPPDVLVLDLNLPGLDGLRVCAQLRERADRRIPVLMLTARDTLADKLKGFEAGADDYLVKPFAGEELLARCLALSQRHRGGEHHLLRIGPLSIDRRGNSAQRDGTMLELHHTAYRILLILAEAWPRTLTRSELMQRLWGDDVPQSDPLRSHLYLLRQALDKPFAWPMLHTVHGVGFKLRDRP
>NZ_CP011130.1|WP_082648253.1|506766_508083_-|HAMP-domain-containing-histidine-kinase
MKRPRRRMRNRLMIAFGGFAVLVAGVFGLYAMVFMYATEDAFFDAALRQEAAALMRARRHDGRWETPRSPYMKVYTDVAQFPDDLRSPYQDEPWRHEYAGRDGRHYHLKTLQASDPAANAWLVAEVSQQLVVRPMRDRILQLLAWSAAAVFALALLIAYWLARRTAAPLARLAAQVGSITPQHLPVLPIPERADDEIGMVAQGVAELIERIRTFIEREQEFTRDASHELRTPLAVIVSTSERLLDEPGLSQAGRQHLMHLRQSASQLEQTVGTLLSLARESQESARTGDPVAVLPLLERVILDQAVLLEGKPIELDIQVSPDTRSVLPEPVLHILLSNLIGNAFAHTEAGVVRIWIEHAQSQDRASLNIVNSGHAIDSDLLATLHRPFQRREGSAGLGLGLAIVRRLCERYRIGLRIQAEDGDTRVELGLAPLGDHVI
>NZ_CP011130.1|WP_148650159.1|505962_506211_+|hypothetical-protein
MYRGEDSHIFERVDWSGQWLLNDLSATRGTLKANAGPMGFVDANGAARIVYRGDEYMQPQASDDNMLHELFYSGGQWLHRDL
>NZ_CP011130.1|WP_148650158.1|504200_505844_+|hypothetical-protein
MKRRKFITAPLAMTAAAAAATLSSGSSVAQQTVLIDANDVGYSPVDGSVTPRSVQGRLREMLSVKDFGAIGDGTSDDSTAFAQAATTAGQVYVPEGDYTVAIAPALGKFFGPGRVKVGSTRVYVHPLPGPVNAIHADVFGLGANEGVDSSAALQAAVDYANDRAIALELPAGRRIRVDSTVVVKLGAAAVGDPPRRFPLKGNNCEIMANVAGPALRLQPQCPVGGTPGLEVGYFQIDNLRFNGYFANQNGLIGRSAIQIGEVGKKFAGFQKCQLRDVFALGFNTPTIRLVGALTRMINFDRVVVNDGGLEIATHENNSFIGDLDFNNCQFGGTVTNPPLKIESAATGAASEIRGIRFFGTIFYGSGTLIYAHKNGRIGDLWFNSLQWEGSSNPVGAHALWIVVDDTADLFQIFIDNPYVVGFNGNAMLFERFGAARVKAVSVRGAKINEIMTAQYRPIVLTQFDDTSILDCDFFGQIAADSCVSVYNAKNVIISRCRSMPNIGTPYFTEISGTSDRVLVANNIADTRVSFIANSAAGSVVSDNNINF
>NZ_CP011130.1|WP_057923389.1|496142_497357_+|tyrosine--tRNA-ligase
MPPTTQEALDLIARGADEILKREELEARLKLGRPLRIKAGFDPTAPDLHIGHTVLLNKMRQFQDLGHQVIFLIGDFTGMIGDPTGKNVTRKPLTREDVLANAETYAEQVFKVLDKERTEVRFNSEWFGKMSAADMIRLAGQHTVARMLERDDFAKRYAGQQSIAIHEFLYPLVQGYDSVALKCDVELGGTDQKFNLLMGRGLQEHHGQPPQIVLTMPLLEGLDGVNKMSKSLGNYIGINEPPIDIVTKTMKIDDVLMWRWIDLLSFEIGIAEAASLKAQIEAGQLNPRDLKLRLARELAARFHGEQAAETAVAGWNAAVRGEGDIASLPLTDVAVPAEGLRIAALLVAAGLTPSNAEGNRKLKERAVKVDGNVVEDPQQAFGPGFEGVLAVGKRNFARVRLVAA
>NZ_CP011130.1|WP_051547931.1|494456_495938_-|M23-family-metallopeptidase
MTVPEQASSVVAERRERLKALREAALKRPVLARHISDGFNGRWSGRQWVQAGLFATLGMMVAAIVPGFSQSTASVRAHEPRQSLALALPPLTLARLKGETGDSWQLVRVNRGQTLGSVFKDMDIPSSTMRQILEQPGAKEALMRMKPGTELGFDMPVNGALRTFRYDKDDSHRIELSLTGDKITQKVIARPTETRTVVLSGKVGKSLFRSARKVGLTAANINTLTDDIFKYDIDFNEDVGSDDRFSVVVEQTWREGELLSTGPILAATFTSEGKLHTGFRFDRGGKPEYFTGDGRPLKKSFIRMPIAYARLTSGFGSRRHPVLGNIRMHKGVDYAAGTGTPIMAAGDARVQFIGWKGGYGRAVILDHGRGYTTLYGHMSNFSKVKPGQRIAQGTVIGYVGSSGLATGPHLHYEFRVNGVHRNPLSVTMPPPEPLSGMALAQFRSQTSVALARIRQVENVIYADAGPAPAPAPAQQATPSIKQVAKKVAKSRRA
>NZ_CP011130.1|WP_057920509.1|514273_515809_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase
MSANARPKPVVLLILDGWGHRDDPADNALAQATLPNWHALLASQAHTLIHTEGRHVGLPDGQMGNSEVGHMNLGAGRIVYQDLTRVDAAIEDGSFYANEELRAACAAAKSSNGTLHVMGLLSPGGVHSHEKHIFAMLELAQREGVARVAVHAFLDGRDMPPKSAAPSLQRLQEVCDRLGNAHIASISGRYYAMDRDKRWDRQLRAWNAMVEADSPEHAPTALAGLEAAYARGETDEFVAPTVIDGATAMADGDAVVFMNFRADRARQLSAAFVDPGFDGYEARRPKLSRFVCLTEYDARLPAPVAFGPDDLHNTLGELLAANGLTQLRIAETEKYAHVTFFFSGGREDPYAGESRILVPSPKVATYDLQPEMSCPEVTAKLVEAIHSGTIDVAICNIANPDMVGHTGDLQAAILAAQAVDKAIGAIAAAVQEVGGALLITADHGNLEMMRDPSTGQPHTAHTVGPVPLVYLGPRKATLRSGGALRDVAPTILDLLGLAQPVEMTGTSLLAR
>NZ_CP011130.1|WP_057920510.1|515808_517077_+|peptidoglycan-DD-metalloendopeptidase-family-protein
MASARGWWLAGVAACSLAMSLGAHAAAQSNSRDAERKLEKIKTELKSVAAERRKLEGQRGDASQQLRQADEQVGHSNRALRDTETRLAREQAALKDLQGKRDALNASLGSKRDELSRLVRAAYAQGNDAPLKLLLSQDKVADSSRILTYHGYVQRDRARRIAELSAQLRELDALERQIVERRASLDSTRKQQRNQLGQLEKDRKTRAALVAQINEKYEDRSTRERELGRDAKGLEQLLAKLRAAAARAEAQRRAAAKAKAEREAREARAAAAAAKAQGKPAPVRKPPVQVASAPAPQVGGLGWPVSGALLAGFGGTMPDGRSSEGLLIGAPAGATVKAVADGTVVYSEWMTGYGLLLIVDHGNGYMSLYANNDALLKDAGATVKKGDAVATVGSSGGHGRPALYFELRRGGQPVNPNTWLRR
>NZ_CP011130.1|WP_082648255.1|517462_518992_+|S41-family-peptidase
MSLRHPLRSLLPLALALGAAPLAFAQQAPTTPPPAAPQSAPQSAPSTAPATPPAETKPADTKPVPKPADTGPTDDTDSPPQPVPPARAPAAKAKPGKDGDGVDSKVPIEEIRRYVAVYNAVKQAYVEPVDDAKLMHAAIRGLLLDLDPHSVYLDKVAAEDFDEQSRGNYDGIGVELQRQPDGTLKVISPIDDTPATRAGIKAGDLIIAIDGKPFKVDEGDSSSTLRGAPGSKVVLTIVREGRDKPFDLTVARETIRVTSVKSRLLEPGYAYLRISAFQADTAADFETQLEKLKTQSGGKLRGLVMDLRSNPGGLLTSAVQIADDLLDSGKIVSTRGRIAISDAEFSATPGDRLDGAPLVVLVDAGSASASEVLAGALRDNGRARVVGSRTFGKGSVQTVLPLDNGDSVKLTTARYYTPSGKSIQALGIVPDVVLRAPKAPDADGRPSYTEATLPGHLHGDEEDTPGTNAGEVLEGDAPIASALAELKKPAGAKTPTAVSKAATPGASKR
>NZ_CP011130.1|WP_057920511.1|519296_519938_-|hypothetical-protein
MTGTPTDTIELKDRRFAVERASVEGRLYDDASGEICWSIEVRGMAMRFGDGEFSQDLSPHFYDEAMPLRIDDWRKLEHSGYAFDLESDDDEGDSLPTLYLCSHLSLPRSQLRLGARRGHRFALDWHGLAEANWDEAFGRELPFRIALDIEFAQQEVRFWHRHDDEDFEAAARAVMARRGLSGEHLRYRDHRRFRDDPDDEHYRLIRAFFAPID
>NZ_CP011130.1|WP_036112538.1|519979_520297_-|DUF1820-family-protein
MPTLYKVTFLNAGKIYELYARKIGSGSLWGFTEVSDLVFDVHEGLVVDPTEERLRDEFGNTKVLHLPMQSIVRIEEVERKGQSAIRDAATGEKVVTPFPFPAKPR
>NZ_CP011130.1|WP_036112535.1|520435_521131_-|rhomboid-family-intramembrane-serine-protease
MFVTIPTRERTRLRWATPLLFALLWLCFIVSAVVLPDPEQRRLMLEWGALSGGLSSPLAWWDAVRDGSLLRLFSALFLHADWAHLLGNLVFLLIFGLPAERAMGPWRLLALFLFGGAVANLAAVIAIGTPDRLIIGASGAVSALIGAYLALFPSAKLGVVVPLGLFLQFVKVPAPLLIGVWAALQVVFTFIGPAFGAVAWSAHLAGFAFGGAFALIARAGIARRLRRKRGY
>NZ_CP011130.1|WP_046659767.1|521396_522764_+|TonB-dependent-receptor
MQPSHRYTRLTAIALGIAGVISFGSAGASGFQIRENSVKNQGRAFAGSAVAKDDASVVSNNPAAMVNLDSTTVRTDVTVIDLTAKFRGGGTSAAGTPLTGGNGGDPGDAQPVPALAIVVPLSGAFDKVTLGASVSAPFGLKTEYDRDWVGRYHAVESDVKTIDLTLSAAVALTDRFSVGFGVVYERAEVTLTSAADLGSLICSGNPACRSPASPFGPQRNDGLVDVTGDDNGLGWLVGFQFKPTDKLSIGYSHRSEIDHDISGTVDFTVPAAVAGAAAGNPVLAARIADGPGGAKLTTPSVDTLSVSYAFTDNFRMMADVQATDWHSLREVDIRRHNALNSQVSFEDFEWEDTMMYALGAEFDLNDAFTLRAGAAYDETPTNDRTRTPRLPDNDRMLYSVGLTWNASEHLSVDAAYTRIEIDSPSIDVRNSTGAHLVGKFKGHADLFGIAAQYKF
>NZ_CP011130.1|WP_057920512.1|522852_523926_-|class-I-SAM-dependent-methyltransferase
MSVSIEADPAKVQQFSARIMEDYGNTLRGAMLYIGDQLGLFKALAQTGAVTLEELTRHTELNARYLREWLGSMATGDYVTYDRHSKRYRLPDEFVPVLADEDSPYFAGGIIQLSVPFVSMAPRIIEAFRHGGGAPEEAYPVETWQGMERMTMPWYKHFLVQHWIPSLTGVKEKLEAGGSVLDFGCGSGLAAITMAQAFPKATVLGCDFHLPSIERARANAHAAGLGDRVRFEVADSDALLGKKFDFVTTFVVIHDAADPQQMMTDLRSSTADDGTYLMVELNLSEELHENMNLFGRVMYPQSTLYCMTCSLSHGGAGLGAFMGETRARDMAAKAGFSRVRKVPSDRPPLPALFELRP
>NZ_CP011130.1|WP_082648256.1|524012_525470_-|adenylosuccinate-lyase-family-protein
MEPQTLNVTPHPAFAARRSCSVSEPALVDDCRHEHSHILDSKVHGGGYAGAASRAIFCGRCRLQRWLDVESVLAMAQAEVHMIPLQAALEIQRSAKLSAMNLDQIADGVSKTGHSLMPLLRALQDNCSPSAREYVHYGATTQDIQDTAQSLEMRDVLDSVDVALDALIAQLAALANAHRGSLMVARTHSIPALPTTFGLKVAGWIDELLRHRDRLGQARQRVLVVQLFGGVGTMAAFGPDAMALLNVFARRLCLGVPHAGWHVARDRVAEFVSALAMMTASLARVADEIRTLNRWEIAEVEVGWSEQQIGSSTMPHKRNPEGCEQVVVMARLAKAQVALALDAMILEHERDYRGTRLEWCAVADVSHYALTALALLSDTIGKLTVNDAAMDRNAHAYGDAICMEAFVFEMAKTLGKSSAYEIIFELTQACQRDRVSIREAVECDPRVLAAVDGGKLARLFEPRAHLGMAETIVDDVLTQVGNRRF
>NZ_CP011130.1|WP_057920513.1|525528_526899_-|adenylosuccinate-lyase
MPSHVTESRIYGGVYSDPEFAAIFCDGNQVQKWLDVERALALTQAQMGLIPHEAAQEIARRAHVELFDLERLGRESRETGHILIPTIWALAERCQDGWGEYVHYGVTTQDILDTGLVLQIAEAWELVLARLRSIQAHLLALARKHRRTPMVARTHGQHALPTTFGYKVAVWVDEIDRHLQRFDEARARVMVGNLTGAVGTMASFGAQGFEIQRRTLASLGLGAPRTSWHSVRDRILEVGGLLVQCAVTFGRIANEIYHLQRTEVDEVREGNAPGKIGSSTMPHKQNPSTADLISALSRLIRAQMVALTDAAFHLHERDGTAWRIEWAALPELFVYTGALLARMDEMLAAGLDVREQRMRDNLDLLGGLILSERVMLALGGRFGKQTAHELVHEISMEARRHDVPFRDALLKDERLRGSFTPQALEDLLDPVTYAGLAVEMVDRVACDATGQPRGRS

Crispr_ID: NZ_CP011130_5

• CRISPR_ID: NZ_CP011130_5
• CRISPR_location: 961915-961989
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_5

Consensus_repeat	Method
GAAAGAAACGCCGTACGCGCGCA	CRISPRCasFinder

spacers of NZ_CP011130_5

>5.1|961938|29|NZ_CP011130|CRISPRCasFinder
TGTCTCCCCACGGATGGCAACGCGTTCTG

CRISPR arrays and Neighbor proteins around NZ_CP011130_5

CRISPR arrays

The CRISPR arrays of NZ_CP011130_5

>merge|NZ_CP011130|5|961915-961989|CRISPRCasFinder
GAAAGAAACGCCGTACGCGCGCATGTCTCCCCACGGATGGCAACGCGTTCTGAAAAGAAACGCCGTACGCGCGCA

>NZ_CP011130|5|4|961915-961989|CRISPRCasFinder
GAAAGAAACGCCGTACGCGCGCA	TGTCTCCCCACGGATGGCAACGCGTTCTG
AAAAGAAACGCCGTACGCGCGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057920706.1|957825_959331_+|TIGR04222-domain-containing-membrane-protein	unknown	unknown	gnl|CDD|275063
NZ_CP011130.1|WP_148650191.1|959344_960043_+|CDP-alcohol-phosphatidyltransferase-family-protein	unknown	unknown	gnl|CDD|223632
NZ_CP011130.1|WP_082648303.1|962161_962599_+|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|276809
NZ_CP011130.1|WP_057923424.1|967858_968599_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046660088.1|970816_971254_-|four-helix-bundle-protein	unknown	unknown	gnl|CDD|319869
NZ_CP011130.1|WP_057920711.1|966224_967301_+|hypothetical-protein	unknown	unknown	gnl|CDD|235906
NZ_CP011130.1|WP_057920700.1|950888_951668_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036111375.1|963703_963976_-|DNA-binding-transcriptional-regulator-Fis	unknown	unknown	gnl|CDD|179020
NZ_CP011130.1|WP_057920701.1|951726_953313_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl|CDD|234854
NZ_CP011130.1|WP_057920705.1|957328_957814_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046660090.1|971282_971768_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl|CDD|235777
NZ_CP011130.1|WP_057920708.1|960716_961676_+|phosphatidate-cytidylyltransferase	unknown	unknown	gnl|CDD|226955
NZ_CP011130.1|WP_057920710.1|964097_965186_-|DUF3426-domain-containing-protein	unknown	unknown	gnl|CDD|378759
NZ_CP011130.1|WP_046660086.1|965213_966134_-|50S-ribosomal-protein-L11-methyltransferase	unknown	unknown	gnl|CDD|283886
NZ_CP011130.1|WP_057920704.1|955985_957332_+|phosphatase-PAP2/dual-specificity-phosphatase-family-protein	unknown	unknown	gnl|CDD|350376
NZ_CP011130.1|WP_057923423.1|962783_963524_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920707.1|960039_960720_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_CP011130.1|WP_057920703.1|954228_955989_+|bifunctional-alpha/beta-hydrolase/class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|371922
NZ_CP011130.1|WP_036111370.1|969456_970824_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	unknown	unknown	gnl|CDD|236307
NZ_CP011130.1|WP_057920702.1|953584_954229_+|CDP-alcohol-phosphatidyltransferase-family-protein	unknown	unknown	gnl|CDD|223632

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057920706.1|957825_959331_+|TIGR04222-domain-containing-membrane-protein	gnl|CDD|275063	TIGR04222, integral_membrane_protein, TIGR04222 domain. The majority of the proteins with a domain as described by this model have an extreme C-terminal sequence that is consists of extremely low-complexity sequence, rich in Ser or in Gly interspersed with Cys. That C-terminal region resembles ribosomal natural product precursors, although there is no evidence that C-terminal regions of these proteins undergo any modification or have any such function.	1.56401e-31
NZ_CP011130.1|WP_057920702.1|953584_954229_+|CDP-alcohol-phosphatidyltransferase-family-protein	gnl|CDD|223632	COG0558, PgsA, Phosphatidylglycerophosphate synthase [Lipid metabolism].	2.15021e-22
NZ_CP011130.1|WP_082648303.1|962161_962599_+|tetratricopeptide-repeat-protein	gnl|CDD|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	3.37449e-09
NZ_CP011130.1|WP_046660088.1|970816_971254_-|four-helix-bundle-protein	gnl|CDD|319869	cd16377, 23S_rRNA_IVP_like, 23S rRNA-intervening sequence protein and similar proteins. A family of functionally uncharacterized bacterial proteins, some of which are encoded by an atypically large intervening sequence present within some 23S rRNA genes. The distantly related bAvd protein, which also forms a homopentamer of four-helix bundles, has been suggested to interact with nucleic acids and a reverse transcriptase.	3.91989e-50
NZ_CP011130.1|WP_057920711.1|966224_967301_+|hypothetical-protein	gnl|CDD|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	0.000113291
NZ_CP011130.1|WP_148650191.1|959344_960043_+|CDP-alcohol-phosphatidyltransferase-family-protein	gnl|CDD|223632	COG0558, PgsA, Phosphatidylglycerophosphate synthase [Lipid metabolism].	2.37035e-17
NZ_CP011130.1|WP_036111375.1|963703_963976_-|DNA-binding-transcriptional-regulator-Fis	gnl|CDD|179020	PRK00430, fis, DNA-binding transcriptional regulator Fis.	5.18575e-36
NZ_CP011130.1|WP_057920701.1|951726_953313_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl|CDD|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0
NZ_CP011130.1|WP_046660090.1|971282_971768_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl|CDD|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	1.0963e-73
NZ_CP011130.1|WP_057920708.1|960716_961676_+|phosphatidate-cytidylyltransferase	gnl|CDD|226955	COG4589, COG4589, Predicted CDP-diglyceride synthetase/phosphatidate cytidylyltransferase [General function prediction only].	1.4838e-131
NZ_CP011130.1|WP_057920710.1|964097_965186_-|DUF3426-domain-containing-protein	gnl|CDD|378759	pfam11906, DUF3426, Protein of unknown function (DUF3426). This family of proteins are functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 262 to 463 amino acids in length.	3.51577e-36
NZ_CP011130.1|WP_046660086.1|965213_966134_-|50S-ribosomal-protein-L11-methyltransferase	gnl|CDD|283886	pfam06325, PrmA, Ribosomal protein L11 methyltransferase (PrmA). This family consists of several Ribosomal protein L11 methyltransferase (EC:2.1.1.-) sequences.	1.26924e-121
NZ_CP011130.1|WP_057920704.1|955985_957332_+|phosphatase-PAP2/dual-specificity-phosphatase-family-protein	gnl|CDD|350376	cd14527, DSP_bac, unknown subfamily of bacterial and plant dual specificity protein phosphatases. This subfamily is composed of uncharacterized bacterial and plant dual-specificity protein phosphatases. DUSPs function as a protein-serine/threonine phosphatases (EC 3.1.3.16) and a protein-tyrosine-phosphatases (EC 3.1.3.48).	1.55062e-38
NZ_CP011130.1|WP_057920707.1|960039_960720_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl|CDD|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	1.28997e-31
NZ_CP011130.1|WP_057920703.1|954228_955989_+|bifunctional-alpha/beta-hydrolase/class-I-SAM-dependent-methyltransferase	gnl|CDD|371922	pfam12147, Methyltransf_20, Putative methyltransferase. This domain is found in bacteria and eukaryotes and is approximately 110 amino acids in length. It is found in association with pfam00561. The family shows homology to methyltransferases.	0
NZ_CP011130.1|WP_036111370.1|969456_970824_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	gnl|CDD|236307	PRK08591, PRK08591, acetyl-CoA carboxylase biotin carboxylase subunit; Validated.	0

Protein sequences

>NZ_CP011130.1|WP_057920708.1|960716_961676_+|phosphatidate-cytidylyltransferase
MSDLIGFVREWPHSVLLFAGVAGVLLIATAIAEWLRWKTRDAPSQVVANLVARIRAWWAMAIVVGLAFAIGRVGMIVLFAIVSLFALREFITLTPTRRSDYYALLAAFYLALPLQYWLVYIDWYGLYTLLIPVYAFLLLPILSTIGGDTTRYLERTAKVQWGLMICVFSISHVPALINLHIPGYEGRNLLLIAFLVIVVQSSDVLQYVWGKLCGKRLIAPKLSPSKTVEGFVGGVASATALGAALWWITPFTPLQAAALALVINLMGFYGGLVMSAIKRDRGIKDWGHMIEGHGGVLDRLDSVCFAAPVFFHLIRYWWV
>NZ_CP011130.1|WP_057920707.1|960039_960720_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MISNLLASSFSGAIRALTGARALWRCSPSSDHRVYYGNHVSHGDFVMIWSALPPALRRQVRPVAGADYWQRDALRRYLIREVFNGVLIERDPAQRKRDAIDTLCDAVDGGSSLILFPEGTRNQGDEPLLPFKSGLYHLAHCRPELEFVPVWIDNLARVMPKGKVLPLPLLCTATFGETLRLHADEDKQAFLDRARNALLALSEHGSGHAAGSAATGDANTRHGAAE
>NZ_CP011130.1|WP_148650191.1|959344_960043_+|CDP-alcohol-phosphatidyltransferase-family-protein
MSDPHDPRPTDSVAPLPSAPGEPARPDWRIRLAARLRSRGATPNGISLFAIGLAALAGLSFFFALRDPPLAGVVLLLFAAVCLQGRMLCNRLDGLLARRGGMVGKAGEVYSDAPDRLADTLIFLGVGYGLAPWLSWASDLGWAASLLSVGTAYVRVLGLACGLREHAQGPMSRRMRMIAMSLAALLSAIGLALGWTQWVEALLAAALAAVALGTAVTIGLRLRSIVRELEAR
>NZ_CP011130.1|WP_057920706.1|957825_959331_+|TIGR04222-domain-containing-membrane-protein
MDENVWTAPRRALWQRLHQYEFGGEHHEAFLTRVAHACQTTREGAQAALEEYRRFCFLAISAGHPVTPSELIDQVWHAHMTDTRDYWQRFCPQVLEQSLHHAPSLGGAQEQERHQQQYRETYISYERFFGDPPAAQWPYPALSRAAQAATHEPQSGRRTPLRFVTPWTLPPRGVGRWAWIWSGACAAAYAWSVSVSADYDPLQWRGYQFLAFYIAAIGCVFTVGGALERRVRGANRRGSVNGEDPVELGFLAAGAERAADVAIVELLDRDALRLDFAGHARDAARTGAWLRANPDGGKQPLPESLREAMWIVQRRQNLDDALGALKQHYAGLGEHLQRKGWWMSSGQALGARLVGTLPIVALVGFGLCKILIGVERGKPVGFLVVLTAFASVLALVRWAFAKRRSRAGDWALHDADRALAKRRESSDVEAGARVALMGTAGLLDSALADYHILRTPVSSSSDGSGGSSSCGSSSNSSSNSSDSGGSSCGSSGCGGCGGGGD
>NZ_CP011130.1|WP_057920705.1|957328_957814_+|hypothetical-protein
MSDPQTPPPSSGDPVATTAFDLRAMASLLAQGRHLRNASLIVLAATLLGLVWPDAGAAAMPAWWLLSLCAGLAQLYYAVRVDFDARLLAALADHDDSANADLHAARRLDASLIALELLPRDRAGRDWPARWRGARGLLRNQALCLLAQLAMLVAAYGRVWL
>NZ_CP011130.1|WP_057920704.1|955985_957332_+|phosphatase-PAP2/dual-specificity-phosphatase-family-protein
MTAATARRPWGRALLWLIFLGPLFFLSYGYANSVAAARVDVPSIVFDWERAMPFWAWTIVPYWSIDLFYGISLFVCRDRRELDTQALRLLSAQVVAISCFLLFPLHFSFTRPETGGVFGWLFDVLLGFDKPFNQAPSLHIVLLIVLWVRFAQHLGGVWRWMLHLWFALIGLSVLTTYQHHFIDLPTGVLAGWLCVWLWPERAAAPWRHAALTRDPQRWKLALIYLIGAGACAYAAIALGGAALWLLWPALSLLLVALNYAVLGADGFQKRDDGRLSMAALWLYAPYLLGAWLNSRWWTRNAPQPVWVIDEVWLGRVPGRDERDGYARVIDVSAELPLRSWRSGDVVRPMLDLVAPSAEQLRQAAIDIESLRGHGEILVCCALGYSRSAAAVAAWLLHSGRAATVDEAIAILRKARPAIVLRDRHRRALGLMTRAAATTRTQVPDGHVA
>NZ_CP011130.1|WP_057920703.1|954228_955989_+|bifunctional-alpha/beta-hydrolase/class-I-SAM-dependent-methyltransferase
MREVQERQFASFDGTSLFYRYWPASAPAAGQPRRAIVLLHRGHEHSGRVQHLVAELGMEDVDFFAWDARGNGRSPGERGDAPGFDALVRDLDRFVAHIGASHGIAVEDTALIAQSVGAVVAATWVHDYAPRLRALVLASPAFKVKLYVPLAVPGLKLMQKLRGNFFVNSYVKPQWLTHDPERVESYRTDPLITRPISVRVLLGLYEAAERIVADAQAITVPTQLLVSGSDFVVHRGPQDRFYERLGSEIKERHLLQGFYHDTLGEKGRVAAINRIRAFVQARFAEPLRRADLLDAHRHGPSFEESEKLSWPPERWSLADLRWRFTRAGLRFGGKFSEGIKLGLDTGFDSGSSLDYVYRDEARGKGPLGRMIDRNYLDAIGWRGIRVRRTHLHELLREAMRRLRAASLPVHAVDIAAGHGRYALEALAGGTERADSIRLRDYSELNVDKGRALIDTLGAGALARFDQGDAFDRNALAALDPRPTLAVVSGLYELFPDNALVRRSLEGLAAAVPPGGFIVYTGQPWHPQLEFIARALTSHRGGEAWVMRRRSQQEMDDLVRAAGFVKIDQRIDAWGIFTVSLAQRVDA
>NZ_CP011130.1|WP_057920702.1|953584_954229_+|CDP-alcohol-phosphatidyltransferase-family-protein
MASIYALKGRFQGLLRPLVRRLYALGVTANQVTTAAAVVSLGVAGLVYWAAPARPWLFALLPLWMFARMAMNAIDGMLAREFGQQSRLGAYLNELCDVVSDSALYLALFAVAGLHPAPLLAFVLLAALTEYAGVLGPMIGAPRRYDGPMGKSDRAFVIGLLGVLLALGWIGARGTELMLIVAGLLCVLTVVRRVRAGLRHDAAQDAVVPQQGEG
>NZ_CP011130.1|WP_057920701.1|951726_953313_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MTSDTSTGTPVHIRRALLSVSDKTGLIELAQALAARGVELLSTGGTAKAIRDAGLAVRDVSEVTGFPEMMDGRVKTLHPLVHGGLLGRAGTDDAVMAQHGIAAIDLLVLNLYPFEKVAADPASSFDDIIENIDIGGPAMLRSAAKNFARVAVATDPAQYAGLIEELNGNDGALSGKTRFALSVAAFNRVAQYDAAISNHLSAIAEDGSAQAFPAQHNASFVKVMDLRYGENPHQLGAFYRDVNPLPGTLATFTQLQGKELSYNNLADADAAWECVRQFETPACVIVKHANPCGVAQGVACGDAYELAYATDPTSAFGGIIAFNTRLDAATAKVILDRQFVEVLIAPDYDDAAIDYARKKANVRVLRIPHGDGRNAQDIKRIGSGLLVQSADLREVGRDELKVVSKLAPTDAQLSDLLFAWRIAKFVKSNAIVYARDHRSIGIGAGQMSRVVSAKIAALKAEEAGLVVPGSVMASDAFFPFRDGIDAAAVAGIKAVIQPGGSMRDNEVIAAADEHGLAMVFTGVRHFRH
>NZ_CP011130.1|WP_057920700.1|950888_951668_-|hypothetical-protein
MSDPSDSDSSKPGASKSGAAGPRAELDVATGLSGRPSLGRNLGRSIARKLTVIAVLLAVMAIWGAWQYTRRQAVDSETLGDYRIDGSSVAVLVVEPDVSLEIGAGLRRDYTVQVARALARRFDQLGYTTREFAARSDEERFGQTTRAADRDAAAQYQAQTMQRLREFNAPVLRVALQDLQYDGRSVSEQHYRVELLDPKTLQPSWRATLTWREGRSQSIALLWHLRKNRLPPPLWDSLADLAIERMRKDGVIAAETRIQ
>NZ_CP011130.1|WP_082648303.1|962161_962599_+|tetratricopeptide-repeat-protein
MTSPPLQMDDAVYERLSRLCEAGNALVAEKRFDAAVTRFNEAWEWVPEPKKDWEASTWILTAIGDCYFRLRDLKSARPVLEYALRCPGGPGNAFIHLRLGQVLLEAGEHDAAADELMRAYKGGGADLFAEDDPKYLAFLATRAQL
>NZ_CP011130.1|WP_057923423.1|962783_963524_-|hypothetical-protein
MRDLTQPGSVLRPFPATEDVFAPGQESLARHLHPLVSIDLAAVRPQWSGWLHLLSPLEPCDGLVGQYTEDEFHAPLLRSNWIGFAVEDGRYRLLGDPRYFLLERSLEQTPAELHAERAELERHYEIENRAYQASRDYYREHGRLVRLNRFGNGPSKDAMPQQLVTQFGGVAESGYNWEETVEFPLEHGVGAGDNGEDVVWPLSPSGRRFEHVASVPGWHYRHTGADLIVLFYEPVEQLALLTFDWS
>NZ_CP011130.1|WP_036111375.1|963703_963976_-|DNA-binding-transcriptional-regulator-Fis
MNALNDRNEAARTGPRVPLRDHVATSIRRYLGDLNGSGTENLYEIALRELEIPLFAEVLQHCDGNQSRAAAMLGIHRATLRKKLREYGLE
>NZ_CP011130.1|WP_057920710.1|964097_965186_-|DUF3426-domain-containing-protein
MFVACPHCGYLVALVVAKDGPTRTCPRCAGALQSQGAANGGDDTANAAQTPNEDAHAVAAESKSVAPATPVAATDIDDIASVLRKKPHKSPVESPAAPSASTRAIDAPATAEVDNQTADSITDSVTDASTDAAPGSDIAAHDIASTQPATSTTASPPADAALTPLNAAVPIARKRPAKRAGKSETAVTSARRAPSFARQHARAAAAPARLHWSGPLLIGVLTIALVLQLLLAQRDELAADARWRPLLAQLCGVLACEIPPWHEPTALTMLNRNVLPVADRAGVLRVNASFRNDARWAQPWPTLVLSLEDVDGRRVGQRAFSPEDYRKGYRAEERIAPGQSAAVQFDVLEPAPHVVAFTFDFR
>NZ_CP011130.1|WP_046660086.1|965213_966134_-|50S-ribosomal-protein-L11-methyltransferase
MPFLELTLRCSEAEQPRYEAALDDVGALAVTMLDADADTSNEHAILEPGVGEIPLWQSMVLSALFPHDADALVLLAALESFDPGLEWTQVRFRQVEDQDWERAWMDQYVPLQFGRRTWIVPWNHDLPDGADAADAAVVRLDPGLAFGSGTHPTTALCLGWLDGLADEGELDGRRVLDFGCGSGILALAALKLGAAHAVGVDNDPQALLATDDNAQRNGVAERIEVHLPPDEPLAQYPVVVANILASALIALADTLAARVAPGGRIALSGILAGQEDEVLARYAADFEQLRADRLEDWMRVTGMRRR
>NZ_CP011130.1|WP_057920711.1|966224_967301_+|hypothetical-protein
MEPTPIRRSFAAAGRAVPSPRPLAWAVAALIALGGSACNREGAATPAAPAAAAPATPTPAATPTTTPPAATALTVKGEVGSLRLRLIDALPPLPKATADSGEASGDCAQAPVSAEARAADAAGWTVFGERDWAGYRAVGVARVGTHLAGMGCVFPDGQVLLFRDGRPVAQVVDTQAGKEDSDAGLQSLEDGLPAPSAEASQVVRRDGADAELRLGDWNGSQLARLVVGADGGLELAALPTIDSYCGQRAKLPRLEAMALPAARERLLAQGWQGRQSDPDADEGADGMRDALRKLGFPEVEGCSGTGMGYCNYHYRNAAGDALQLTSAGEYVPPGVDQAEANWPRVAGYSVRCAAPKAD
>NZ_CP011130.1|WP_057923424.1|967858_968599_+|hypothetical-protein
MAQSPLRQQFEQARDLYSFAQSLRSRADAGEPEAIWLLTRVYDYCANYANAPVDYGNDTRAIEAMKLRTSAAMVAARSRVSSRCARFVPEDNLSFSMILVKRVEAAKSGSLPAEASLLAAGKPLEKTEEYRNDLVERVVRSKDPEAYSALSPGMGIASSGRSAGFTRAAGTQFAELAWQLAACRLGQDCSAKGSLMTSYCANGGICSQDPEQDFAGFVYDAAIPRQGAQVVEEMVDSLTGEKRMVQ
>NZ_CP011130.1|WP_036111370.1|969456_970824_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit
MLDKVVIANRGEIALRILRACHALGIRTVAVHSTVDRNLKHVAMADESVCIGPAPSSDSYLNMASIIAAAEVTDAQAIHPGYGFLSENADFAERVEQSGFIFIGPRAETIRLMGDKVEAIRAMKEAGVPCVPGSGGPLGDDNAANIKIAREIGYPIIVKAAGGGGGRGMRVVHTEAHLNAAIQTTKSEAKAAFGNDMVYMEKFLENPRHVEIQVLADGQGNAIHLGERDCSMQRRHQKVVEEAPAPGITVEQRAEIGKVCVEACIRIGYRGAGTFEFLYENGRFYFIEMNTRIQVEHPVTELVTGIDLVREQLMIAAGRKLSIKQSDIVLDGHAIECRINAEDPETFMPCPGLIQHFHAPGGPGVRVDSHIYEGYRVPPNYDSMIGKLIVHGPDRDTAIARMRVALSEMVVDGIKTNIPLQQRILSDAGFQQGGMNIHYLEKRLKEQKEKTISIV
>NZ_CP011130.1|WP_046660088.1|970816_971254_-|four-helix-bundle-protein
MIRDSDKQRPHERLEVWRDAMALVESIYRVTASFPDTERLGLSMQLRRAAVSVPSNIAEGAARRSRPEYLRFLAMARGSLAELSTQYEIARRLGYLTENDTDTDLLDRTFARLNALIRSLGSSPRVVSQTPALHESQISNPESHA
>NZ_CP011130.1|WP_046660090.1|971282_971768_-|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MDLRKIKKLIDLLEESNLAEIEIKEGEESVRLARTPKGGYAMPQPQPMYAPAPEQRPAAQAMPMSSPTEAATGGSAKPASDLPDGHVVRAPMVGTFYSSPAPDKPPFVAVGQSVKAGDTLAVIEAMKMFNPIEADVSGTVLKIMAESGQPIEFDQPLFVIG

Crispr_ID: NZ_CP011130_6

• CRISPR_ID: NZ_CP011130_6
• CRISPR_location: 1149460-1149564
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: cas3

Consensus repeat of NZ_CP011130_6

Consensus_repeat	Method
CTCTCGATATGCGGCGCCCCGCGTA	CRISPRCasFinder

spacers of NZ_CP011130_6

>6.1|1149485|55|NZ_CP011130|CRISPRCasFinder
GGCAGTTGGACAGCGACGAAAGGCGCCGAAGCGCCCCTCGCAAGTCGCCGAGGCA

CRISPR arrays and Neighbor proteins around NZ_CP011130_6

CRISPR arrays

The CRISPR arrays of NZ_CP011130_6

>merge|NZ_CP011130|6|1149460-1149564|CRISPRCasFinder
CTCTCGATATGCGGCGCCCCGCGTAGGCAGTTGGACAGCGACGAAAGGCGCCGAAGCGCCCCTCGCAAGTCGCCGAGGCACTCTCGATACGCGGCGCCCCGCGTA

>NZ_CP011130|6|5|1149460-1149564|CRISPRCasFinder
CTCTCGATATGCGGCGCCCCGCGTA	GGCAGTTGGACAGCGACGAAAGGCGCCGAAGCGCCCCTCGCAAGTCGCCGAGGCA
CTCTCGATACGCGGCGCCCCGCGTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_036108754.1|1135339_1137520_+|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase	unknown	unknown	gnl|CDD|223394
NZ_CP011130.1|WP_036108751.1|1137653_1138037_+|RidA-family-protein	unknown	unknown	gnl|CDD|129116
NZ_CP011130.1|WP_036108738.1|1149909_1150152_+|type-B-50S-ribosomal-protein-L31	unknown	unknown	gnl|CDD|234969
NZ_CP011130.1|WP_057920786.1|1146957_1147596_+|calcium-binding-protein	unknown	unknown	gnl|CDD|380205
NZ_CP011130.1|WP_057920785.1|1144690_1146811_+|ATP-dependent-DNA-helicase-RecG	cas3	cd09639_cas3_CAS-I	gnl|CDD|236794
NZ_CP011130.1|WP_036108732.1|1159345_1160404_+|pilus-assembly-protein-PilM	unknown	unknown	gnl|CDD|378558
NZ_CP011130.1|WP_051547488.1|1138255_1139317_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|378890
NZ_CP011130.1|WP_057920792.1|1156264_1158838_-|penicillin-binding-protein-1A	unknown	unknown	gnl|CDD|227342
NZ_CP011130.1|WP_036108820.1|1155361_1156015_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920787.1|1147885_1148467_+|DUF4166-domain-containing-protein	unknown	unknown	gnl|CDD|379359
NZ_CP011130.1|WP_051547487.1|1150683_1151991_+|citrate-synthase	unknown	unknown	gnl|CDD|180164
NZ_CP011130.1|WP_187313336.1|1139498_1140731_+|right-handed-parallel-beta-helix-repeat-containing-protein	unknown	unknown	gnl|CDD|163517
NZ_CP011130.1|WP_057920793.1|1160403_1161219_+|PilN-domain-containing-protein	unknown	unknown	gnl|CDD|225707
NZ_CP011130.1|WP_057920788.1|1148463_1149405_+|nucleoside-hydrolase	unknown	unknown	gnl|CDD|239115
NZ_CP011130.1|WP_057920784.1|1142141_1144583_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|224544
NZ_CP011130.1|WP_148650206.1|1153922_1154651_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920789.1|1152281_1152671_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920783.1|1140779_1141955_+|hypothetical-protein	unknown	unknown	gnl|CDD|163518
NZ_CP011130.1|WP_148650205.1|1152835_1153687_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920794.1|1161215_1161938_+|type-4a-pilus-biogenesis-protein-PilO	unknown	unknown	gnl|CDD|225708

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP011130.1|WP_057920785.1|1144690_1146811_+|ATP-dependent-DNA-helicase-RecG	cas3	cd09639_cas3_CAS-I	2.7e-11	37.8	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_036108754.1|1135339_1137520_+|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase	gnl|CDD|223394	COG0317, SpoT, Guanosine polyphosphate pyrophosphohydrolases/synthetases [Signal transduction mechanisms / Transcription].	0
NZ_CP011130.1|WP_036108751.1|1137653_1138037_+|RidA-family-protein	gnl|CDD|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	2.7313e-59
NZ_CP011130.1|WP_036108738.1|1149909_1150152_+|type-B-50S-ribosomal-protein-L31	gnl|CDD|234969	PRK01678, rpmE2, type B 50S ribosomal protein L31.	4.66939e-45
NZ_CP011130.1|WP_057920786.1|1146957_1147596_+|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.	3.04668e-12
NZ_CP011130.1|WP_057920785.1|1144690_1146811_+|ATP-dependent-DNA-helicase-RecG	gnl|CDD|236794	PRK10917, PRK10917, ATP-dependent DNA helicase RecG; Provisional.	0
NZ_CP011130.1|WP_036108732.1|1159345_1160404_+|pilus-assembly-protein-PilM	gnl|CDD|378558	pfam11104, PilM_2, Type IV pilus assembly protein PilM;. The type IV pilus assembly protein PilM is required for competency and pilus biogenesis. It binds to PilN and ATP.	1.86376e-168
NZ_CP011130.1|WP_051547488.1|1138255_1139317_-|AraC-family-transcriptional-regulator	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].	6.6586e-37
NZ_CP011130.1|WP_057920792.1|1156264_1158838_-|penicillin-binding-protein-1A	gnl|CDD|227342	COG5009, MrcA, Membrane carboxypeptidase/penicillin-binding protein [Cell envelope biogenesis, outer membrane].	0
NZ_CP011130.1|WP_057920787.1|1147885_1148467_+|DUF4166-domain-containing-protein	gnl|CDD|379359	pfam13761, DUF4166, Domain of unknown function (DUF4166). This domain is often found at the C-terminus of proteins containing pfam03435.	2.08409e-12
NZ_CP011130.1|WP_051547487.1|1150683_1151991_+|citrate-synthase	gnl|CDD|180164	PRK05614, gltA, citrate synthase.	0
NZ_CP011130.1|WP_187313336.1|1139498_1140731_+|right-handed-parallel-beta-helix-repeat-containing-protein	gnl|CDD|163517	TIGR03805, beta_helix_1, parallel beta-helix repeat-containing protein. Members of this protein family contain a tandem pair of beta-helix repeats (see TIGR03804). Each repeat is expected to consist of three beta strands that form a single turn as they form a right-handed helix of stacked beta-structure. Member proteinsa occur regularly in two-gene pairs along with another uncharacterized protein family; both protein families exhibit either lipoprotein or regular signal peptides, suggesting transit through the plasma membrane, and the two may be fused. The function of the pair is unknown. [Unknown function, General].	4.62819e-145
NZ_CP011130.1|WP_057920788.1|1148463_1149405_+|nucleoside-hydrolase	gnl|CDD|239115	cd02649, nuc_hydro_CeIAG, nuc_hydro_CeIAG: Nucleoside hydrolases similar to the inosine-adenosine-guanosine-preferring nucleoside hydrolase from Caenorhabditis elegans. Nucleoside hydrolases cleave the N-glycosidic bond in nucleosides generating ribose and the respective base. These enzymes vary in their substrate specificity. This group contains eukaryotic, bacterial and archeal proteins similar to the purine-preferring nucleoside hydrolase (IAG-NH) from C. elegans and the salivary purine nucleosidase from Aedes aegypti. C. elegans IAG-NH exhibits a high affinity for the substrate analogue p-nitrophenylriboside (p-NPR). .	5.55356e-115
NZ_CP011130.1|WP_057920784.1|1142141_1144583_+|TonB-dependent-receptor	gnl|CDD|224544	COG1629, CirA, Outer membrane receptor proteins, mostly Fe transport [Inorganic ion transport and metabolism].	2.77302e-46
NZ_CP011130.1|WP_057920793.1|1160403_1161219_+|PilN-domain-containing-protein	gnl|CDD|225707	COG3166, PilN, Tfp pilus assembly protein PilN [Cell motility and secretion / Intracellular trafficking and secretion].	8.89093e-51
NZ_CP011130.1|WP_057920783.1|1140779_1141955_+|hypothetical-protein	gnl|CDD|163518	TIGR03806, chp_HNE_0200, conserved hypothetical protein, HNE_0200 family. The model TIGR03805 describes an uncharacterized protein family that contains repeats associated with the formation of a right-handed helical stack of parallel beta strands, homologous to those found in a number of carbohydrate-binding proteins and sugar hydrolases. This model describes another uncharacterized protein family, found in the same species as TIGR03805 member proteins, usually as the adjacent gene or in a fusion protein. An example is HNE_0200 from Hyphomonas neptunium ATCC 15444. Sometimes two members of this family are with a single member of TIGR03805. The function is unknown. [Hypothetical proteins, Conserved].	3.84264e-139
NZ_CP011130.1|WP_057920794.1|1161215_1161938_+|type-4a-pilus-biogenesis-protein-PilO	gnl|CDD|225708	COG3167, PilO, Tfp pilus assembly protein PilO [Cell motility and secretion / Intracellular trafficking and secretion].	2.41423e-76

Protein sequences

>NZ_CP011130.1|WP_057920788.1|1148463_1149405_+|nucleoside-hydrolase
MTDRIPLLIDTDPGVDDALALLMAFNDTRHEVVGLTIAAGNVGLKHTVANALKLCEVAGVDVPVFAGTAAPLLHPSPDAGYVHGQDGFGDVGYEPAKRQVEAEHAALAILRLSHEHAGKLLLVALGPLTNVALALKLDPTLPQRIARLVVMGGAVTCQGNITPAAEFNIYFDPEAAHIVFEAFERIDLADWEAVVAHGLHHDRVVEWLKAGSTRGQFYERISEKTRLWSIDRRGDHWHAADALAMAFALEPDGALDVQARPLSIELEGTHSRGATIVDWRRQEGREDRVAILMQYDQKRFERLIRDALAASPA
>NZ_CP011130.1|WP_057920787.1|1147885_1148467_+|DUF4166-domain-containing-protein
MLQALHRDGGTLGGQIALSTGTGLAGAIGRRLARKLGIPIDRPRRGFRVDIVHDQQQMQWRRRFDDGSELISIFRPVGRYPDGHWLESTGPARMRLGVDLDGGGWRWRLLGVDVRGLRLPLFLFPRTDAYKRIEPGGEGERYRFAVTFSLFPFGELLRYEGALHAIPAVTASTADPAGAAIAAAHSSAERVIP
>NZ_CP011130.1|WP_057920786.1|1146957_1147596_+|calcium-binding-protein
MPIAFDQPPTAGGANVHSPAQTRSVSDFTWSPATRAANARLRRNVPGLFSTVTGTAGDDVLYGSHQADLIEGLEGADSLYGLGGDDALYGGSGDNALLGGSGEDRLYGGEGNDFYYFNIGDGQDRVYSADSLGQFLEIVHFGAGIDPAQVTLARVGADLVVNHGNGDVVTVVGFFPGGEDPWPRGVDEIWFQDGTTWDVAEILARLPPGQGL
>NZ_CP011130.1|WP_057920785.1|1144690_1146811_+|ATP-dependent-DNA-helicase-RecG
MPSRKDGPSVDLHTQPMPRMPGVGPRVAEKLAARGLTTLQDFWLQLPRQYEDRTQITPIRLLQPGVAAQVEGRVEGVERGFRYKPMLRVAIGDDSRATVVLRFFHFRAAQVAQFQVGARVRLYGTPKPGQHGLEIVHPSYRVFDDDSDEVALGEQLDPVYPAIEGIGPATLRRLIGYALDRLPDDGSLELIPRELRERLQLPTLREALLTVHRPAVDADVAALIAGRHPAQRRLALEELLAHHLSLRRQRISQQAHKARPLKQMPLAERLRKSLPFKLTGAQKRVFDEIRVDLAKPSPMLRLVQGDVGSGKTVVAALAAMIAVQHGRQAALMAPTELLAEQHLNNLRRWLEPLGVRVAWLAGKVTGRARKAVLEQVANGEAQMVVGTHALMQEGVAFADLALAIVDEQHRFGVHQRLALRDKGAGGAVGKDAIVPHQLVMTATPIPRTLAMTAYADLDVSAIDELPPGRTPVQTVALSEERRPELVQRIRGACAEGRQAYWVCTLIDDSDEVIAQAAQTTFEELSVQLAPLRVGLVHGRMKAKEKQEVMRAFKDGELDLMVATTVIEVGVDVPNASLMIIENAERLGLAQLHQLRGRVGRGSAASSCVLLYRSPLSGLARQRLETMRQTVDGFVIAEKDLELRGPGELLGTRQTGLAGFRVADLARDADLLPLVQDLGEDLLKTSPELAERIVSRWVGGAVRYASA
>NZ_CP011130.1|WP_057920784.1|1142141_1144583_+|TonB-dependent-receptor
MSLRKHRLVTATATAIAALCGGGLVLAAPAAFAQSAEPNQASAPKELDKITVTAQSREQELQDVPIALQVVTDQLIDDTAAQDLGDLDSFVPGLVVDSQQPTQPGFELRGISTDDFGIGTDPAVGVYVDGVYAGRGGGVLLPFTDVERIEVLKGPQGTLFGRNTAAGAISIITRKPDASATEVKTKLRIGNYGKQYLEGMLNLPTGEDSAFRFNALVNHADGWIQDAATGRDLNPENNWATRAAFKTRFGERTSALISWDHESLDQLGQATTGIIALPPAPGLAPLPVDESAYLDPRKVPTMSDAEGNEESRRFDGVTLIVDHGFDWGGFTSTTSWRDYDSVNRVEEDGTNRNYLYVDSTNTESNRSYYQEFKFSGSTDKLDWIAGASYFKEDARQTSEVNALTDSVDTIVHNLGLAPTPNGYLFGYVDQQLDALGIPIHLLGHRWNETFRNTLDTKAYAVFGDVIWHATDKLNLTVGLRYTRDEKDFSWHNDPRYAPGLDAALDQLEGLGFFDLAGIPRDFFVFDIAFIDPPAMLNKGLTNRDKRSWSDFSPRFVADYHINDDTMVFASLAKGYKAGGFNSLQIGSSFENEDVWNFETGIKKSFPDQRLQLNASAFYYVYDNRQAVRLDSSTSIPRFVVDTSDLEAYGLDFDMRWQATDNFGLDFNASFIDSTYKNYVTSDGIDASGDPTGLPYWSAAGGAYYVVNLADHGDLRFSLRHSYRGKVRCSAESQAQNRCGVSPALDLGEAQNRTDLRIGWTSPQGRWGLAAYGNNLFDNQYINSLGTYGKNVLGTVGARVSEPRTFGVEFSAKY
>NZ_CP011130.1|WP_057920783.1|1140779_1141955_+|hypothetical-protein
MRYVFAVAMSLLVAGCGKPTADVTPQASSQAVNIAADSPWPAVHFFADGQPADLAEWNLLRVADGRLRLNRDVLPYDLNTALFSDYAHKLRTVWMPKGQAAQFDAQREFDFPIGTIFSKTFYYPRGEGDAVLRSADDGPDLAGGGLQLSKVRLIETRLLVRRQDGWIALPYVWNAEQTQAKLMRGGELVSLQLVASDGSREQAQYTVPDQNQCAGCHGTDMKSKALHPLGPRARHLNRDFAYDDGVANQLAHWTKVGYLHGAPEPASAPRDANWRDPDAPLEARARAYLDINCGHCHSPTGPGNTSGLWLDASTQEPLRLGRCKLPIAAGKGTGDRRHDIVPGKPDESILTYRMVSDDPSVMMPELGRSVVHAEGVQLIRDWIAAQQGTCG
>NZ_CP011130.1|WP_187313336.1|1139498_1140731_+|right-handed-parallel-beta-helix-repeat-containing-protein
MNQPIRASVLALAVAALTAACGPEQAQHTPTAQVAAGDAGFADTFRTRLLDAKDGDVIEVPAGRYTFDRSLTLRVDGVTIRGAGPDKSVLSFKGQKAGAEGLLVNASRFTLENIAIEDSKGDGLKVNEGEHITIRNVRVEWTGGPSTKNGAYGLYPVKTRNVLIENSVAIGASDAGIYVGQSRDVIVRNSRVEFNVAGIEIENTVNADVYDNVATNNTGGILVFNMPALSQQGGAIRVFKNKVFKNNTANFGAKGTPVASVPAGSGMVVNSNDDVEIFDNDISDNATTNIIVSSVYSTGYKDDKAAKDFDPYPERISIYGNRLSGGGDSPDGLDLKALKTAIYGLSGHFPDVLWDGYANKDRKEGPQICIRDVSGVVNADGPGSYKNPSQDTKPYECELPKLPAIDLKRG
>NZ_CP011130.1|WP_051547488.1|1138255_1139317_-|AraC-family-transcriptional-regulator
MRQSSDQDKARADIALMSPNLLWGLLETADRIGAPSDDWFAGTGLSRAQVSDPGVRLPDRPTAVVVERALKVLPPTIGLDLGRDQHIGNFGLLGLAMTTAATFGEALQIGLRFTPVVGSLMRFVESASESGTLALAGQMTLAYPSIHRFVAEEFFSSCLALARGLVGTTLRPLRIEFSYPAPAYREHYDEVFDCPVAFEQPQDRLVLDANWLAVPLPTHNPIASRQVLALCEAQMPDAAVPGEVTAAVERLLRAQLPQDPKLAGIAAQLHVSERTLRRQLTNEGTSFHDIHDRLRIDRAYALLRERNLTIASVGAAIGYKDPRDFRRAFKRLTGQTPRALREHLLAEMAGERR
>NZ_CP011130.1|WP_036108751.1|1137653_1138037_+|RidA-family-protein
MSREIIQTDQAPAAIGPYSQAVRVGDTVYLSGQIPLDPSSGLVIEGDIEAQAHRAFRNLQAVCEAAGGSLADIARLGLYLTDLSAFGKVNAVMGEYFNAPFPARSTVEVSALPRGVAFEVDAIMVLR
>NZ_CP011130.1|WP_036108754.1|1135339_1137520_+|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase
MTPAEPALKTYPAAAEDTELPDYVRELELAAHYLPEAQRHQLRRAWAVGAAAHAGQTRKSGEPYITHPVAVAKVLAEQGLDVETLVAAILHDTIEDTPLTRECLATEFGPTVAELVDGVTKLDKLQFRDRQEAAAESFRKMLLAMARDLRVILIKLADRLHNMRTLGAQSAEARERIARETLEIYAPIAQRLGMNLIKAELQDLGFRALHPWRHAVVEKRIRTQPVVRRESLVQIEAHLAQRLAKEKLQHRLISRVKSPWSIYTKMHHEHKSFTQVMDVFGFRIVVKSVPDCYHALGVAHSAYKPLDSRFRDFIAIPKANGYQSLHTVLFGPYGSPVEVQIRTEDMDLIAERGIAAHWSYKHGGEGPNSAQSRAHSWIASLVESQRSTGSSLEFLENVKVDLFPDEVYLFTPKGDILSLPRNSTALDFAYAVHTDVGNRAVAARVDGKLVPLRTKLASGQRVEIITAKSSTPKPQWLEFVVSGKARTSIRQQLKQLEHEDAVQLGHRMLDRALEVLETSLDRTPAQRLDAYLAENRYPRLEALLADIALGNRMPNQVALALAREAPGKARGRSIDRPRLPEDKILITGAERGVISFANCCLPLPGDEIMGYHTAGKGIVVHRLDCPNVAEYRKSPDRWVAIGWDRQVSGDFAAALRIEVDNRPGSLAQVAAAIAEAESNIDRVEYLERDSNIAIMRFAIEVHDRKHLADVMRRVRRLAVVLGVQRM
>NZ_CP011130.1|WP_036108738.1|1149909_1150152_+|type-B-50S-ribosomal-protein-L31
MKAGIHPEYRSVVFQDVTTDFQIVTRSTLSSKETIKIDGTEYPLIKVDISSASHPFYTGKHKIMDTSGRVDKFRKRYAQK
>NZ_CP011130.1|WP_051547487.1|1150683_1151991_+|citrate-synthase
MSEDSSKTRLDQVTVTAGDKNFALPVQHPVLGAPCVDIAKLPKETGMFTYDPGFTATASCKSAITYIDGDAGVLLYRGYPIEQLAEKSNFLEVAYLLMNGELPTQTEFSKFEHEVTHHTMMHEAFRTFLYGFRHDAHPMAMLVGMLGSMASFYHNELDLEDPEQRRLAAIRLIAKVPTIAAACHRYSIGWPIRYPKNSLDYTTRFLHMLFEVPSEPLELSPVAAKAMDLLFILHADHEQNASTSTVRLVGSTGANPYVSVASGVAALWGPAHGGANEAVLKMLNEIGRPENVKSAVEKAKDKESGFRLMGFGHRVYKNYDPRAALVRKMTHDVLGELGINDPLLDVAMKLEEAALKDDYFVQRKLYPNVDFYSGIIYKALGIPVEMFTVMFAIARTAGWVSHWLEQQNDPENKIGRPRQIYTGHGVRDYVGADKR
>NZ_CP011130.1|WP_057920789.1|1152281_1152671_-|hypothetical-protein
MRLHGPALLCLLTLSSAAVAADKPAATSLTKLYQSYENAGNSALSMAEYDTRVRFSAVVLDQTTSMDDTPILQATEAGEEAEYARLMGEDEAQSKKLGALKIGAKFTATCTVGFTSGTDYLSLKDCTVE
>NZ_CP011130.1|WP_148650205.1|1152835_1153687_-|hypothetical-protein
MADGTVLVQSLTDDDARATVTPRAGQEHYVLEMLWGRFPVKVSAECWRRPAAQFENCAEIGPREDTQAQKDERAEDERKELERKRRLAARTAWMRPEMTQQSIVSIISKTMRDQQAWMRTPAARLIADNFACDTSNAGLPKITAEAQEKYAQARRIGAYDAQGEPVLIEAAQLGNWRAVTTLFNVAMYGEDWESAQPLVAWLLQRDAPAGYNKLAELHGTIASYEHGHASSADQDLVTALRWRAAQAGDPGAQRDMSDYFKERDPQLSERLMQCALERFPDLR
>NZ_CP011130.1|WP_148650206.1|1153922_1154651_-|hypothetical-protein
MRADYDALLASQRMSAAQLPYADYAYLRLLFEATRDGGYWNLHWAITDREPNSDAIWAQWRSLRGATPTGITATAECDELSALYAFLARRGGVRNVGLFWPTSNHTVAVWRIASTPRETRIVVPTTQIFLTQSDSFGTRGFDPWKQAKIYEYGRRDIADDARLPPALVAFFLAQNDKYARASGLSLQHMRQLRDGVLDGSLGADQAARQAQAQRDRIASSAIDDRNAYAHFIRDLQTSTRAP
>NZ_CP011130.1|WP_036108820.1|1155361_1156015_-|hypothetical-protein
MHQARQHAHQHAQTRIRERRHRLAHEAARLIAESGIRDYHQAKLKAAERLGIFDDASLPRNREIEDALREYQRLFQRDNLDGLRQRREAALRALEFFAPFEPRLVGPVLDGTADARSPVALHLYSDDPDAVSMFLDHHLIPAEARERRLRLDRERSEDFPVWVFSAEELTFDLTVLPLDVLRQAPLSQVDEKPMKRAAANQVRQLLADEEISEFERG
>NZ_CP011130.1|WP_057920792.1|1156264_1158838_-|penicillin-binding-protein-1A
MSRIRRWLRWALYAFIGVALLGAIALGTLYYLIVPKLPDVETLRTIELQEPMYVYARDGRLMAMFGETRRYPIAIEDVPERQKQAFIAIEDSRFYQHHGIDYKGIGRAIWLLATTDDKRVPGGSTITQQVARQFFLSSEYSYKRKLGEMLLAMRMEQELSKDEIFELYLNKSFFGNRAYGVGAAAEFYYGKKMSELSLDEMASLAGIPKFPSSGNPLSNPERAKIRRDYILDRMAEQHFISAEEAAQAKAVPMHATPHERPVEVYAPYVAEMVRQEMVARYGAEALTKGYHVTTTIDPTLQIAADKAIRDGLSVYDRRHGWHGVEQHFDLAAGDDAAAIRVRLRGIPAQANLLPAVVLSTSGSQATVALGDGTELTLTDKQGFGGRSPGSLLTRGDLVRVARLETPAKPVAEPKPGEAAPAAPAAPAEPPIVTYRLDQLPQAQAALVSLEPADGALRALSGGYSFAGAKFNRATQARRQPGSSFKPFVYAAAFERGYNPASIVLDAPVVFKDRRGHLWRPQNDGGNFAGPMRVREAMVQSRNLVSVRLLDAISVDFARKYISHFGFDPEQLPPNLSMSLGTASLTPLSVARGYSVFANGGFRITPWFIDEVKDRAGAVVFKEKPATACPQCGGRGGTSSAALPVSNVVDGFDLGPAPGADSAAKKPDPKDKASKDKKPAEPEKKPLTPAEMAALNLAPRAIDDRIAYQIVSMLRDVVKRGTGTAAKVLGREDVGGKTGSTNDHRDAWFSGFGGPYVTTVWVGRDNYKSLGYREYGGKAALPIWIDYMRVALKDKPIQPNEPPQGMVKVSVAGNGALIPDGTGGVIEWVKAEDLERMQTYTDYGTEDAAPSEESFDIF
>NZ_CP011130.1|WP_036108732.1|1159345_1160404_+|pilus-assembly-protein-PilM
MGLITKSQPALVGVDISSTAVKLLQLSRVGNRYRVEHYAVEPLPPNAVVEKNIVEVEAVGEAIKRAVARSGTRVKHAAAAVAGSSVITRVIGMPNDLDEDEMESQIELEAANYVPYPIDEVNHDFEILGPMPGASDMVQVLLAASRSENVEVRASALELGGLTPRVMDVEAFAIENAFALLADTLSGPRDGLVALVDSGATMTTLNVLRNGRSLYHREQVFGGKQLTDEVMRRYGLSYEEAGLAKRQGGLPESYQAEVLEPFKEAMVQQVSRLLQFFYAGSEFNRVDQIVLAGGGASIPRIAEMVEEQLGVPTTVANPLAHMTLGPRVQAHALAQDAPALMIACGLALRSFD
>NZ_CP011130.1|WP_057920793.1|1160403_1161219_+|PilN-domain-containing-protein
MARINLLPWRAERRKARQKEFGAIMLLSILAALALSVLIVFYYSSEISGQRKRNAFLDTQIAEVEKKITEIEELDKKKAKLLARKEVIEKLQSNRSQMVHLFDSLVRTIPDGAVLTAIKQDAETLTLEGRAQSNARVSTYMRNLEVSGWMTKPDLSIIEAKGNEKGLPYEFKLQVKLANPNAPKDEDGDGFPDAPAPGDAAAVPADGTAAPAGTTAPAAAPAGTAPAAPADAKPGAAPATTPAKPAPAPAQPAAAPVKPAPAAPTKTGAAS
>NZ_CP011130.1|WP_057920794.1|1161215_1161938_+|type-4a-pilus-biogenesis-protein-PilO
MSKKASMKNLDINNIGGWPRNAQIVFCAAVGLIIVGLAWWLFVSDKRTELEKLERQEAELRTTFETKQGRAANLEPLKQQLAQMEQQLQQMLRQLPSKTEMPDLIVDISQTALATGISNELFQPGAEVPKEFYAEKPIALRMVGTYHQFGAFVSGVASLPRVVIMTMHDISLKPKGKNNKDAVGGITPNSPLELAGTVKTYRYLDEDEMAAQAQTAEDAAGGNKSGSKDKKKADDKKGAD

Crispr_ID: NZ_CP011130_7

• CRISPR_ID: NZ_CP011130_7
• CRISPR_location: 1390471-1390572
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_7

Consensus_repeat	Method
CCCTTCTCCCGCAAGCGGGAGAAGG	CRISPRCasFinder

spacers of NZ_CP011130_7

>7.1|1390496|52|NZ_CP011130|CRISPRCasFinder
TGGCCCGAAGGGCCGGATGAGGGGCTGCAAGCGCTGGTAGACCCTCACCCAA

CRISPR arrays and Neighbor proteins around NZ_CP011130_7

CRISPR arrays

The CRISPR arrays of NZ_CP011130_7

>merge|NZ_CP011130|7|1390471-1390572|CRISPRCasFinder
CCCTTCTCCCGCAAGCGGGAGAAGGTGGCCCGAAGGGCCGGATGAGGGGCTGCAAGCGCTGGTAGACCCTCACCCAAACCCTCTCCCGCAAGCGGGAGAAGG

>NZ_CP011130|7|6|1390471-1390572|CRISPRCasFinder
CCCTTCTCCCGCAAGCGGGAGAAGG	TGGCCCGAAGGGCCGGATGAGGGGCTGCAAGCGCTGGTAGACCCTCACCCAA
ACCCTCTCCCGCAAGCGGGAGAAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057920895.1|1388695_1390462_+|phosphoenolpyruvate-carboxykinase-(GTP)	unknown	unknown	gnl|CDD|235256
NZ_CP011130.1|WP_057920892.1|1382836_1383298_+|hypothetical-protein	unknown	unknown	gnl|CDD|375655
NZ_CP011130.1|WP_148650224.1|1368165_1382835_+|putative-Ig-domain-containing-protein	unknown	unknown	gnl|CDD|225750
NZ_CP011130.1|WP_036114493.1|1365306_1365906_-|NAD(P)H:quinone-oxidoreductase	unknown	unknown	gnl|CDD|179647
NZ_CP011130.1|WP_148650223.1|1366076_1366346_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057920890.1|1366869_1368030_+|MFS-transporter	unknown	unknown	gnl|CDD|225371
NZ_CP011130.1|WP_036114457.1|1390696_1391284_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|236608
NZ_CP011130.1|WP_046655702.1|1401206_1404191_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP011130.1|WP_082648343.1|1406207_1407152_-|Hsp33-family-molecular-chaperone-HslO	unknown	unknown	gnl|CDD|238278
NZ_CP011130.1|WP_036114455.1|1394685_1397589_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP011130.1|WP_057923448.1|1407354_1408116_+|monofunctional-biosynthetic-peptidoglycan-transglycosylase	unknown	unknown	gnl|CDD|234603
NZ_CP011130.1|WP_057920897.1|1392098_1393052_+|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|372574
NZ_CP011130.1|WP_082124145.1|1387932_1388616_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP011130.1|WP_057920894.1|1384148_1384625_-|DUF4442-domain-containing-protein	unknown	unknown	gnl|CDD|373120
NZ_CP011130.1|WP_057920893.1|1383563_1383968_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_187313401.1|1405214_1406030_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_082648342.1|1393176_1394523_+|aspartyl/asparaginyl-beta-hydroxylase-domain-containing-protein	unknown	unknown	gnl|CDD|377460
NZ_CP011130.1|WP_148650225.1|1391325_1392081_+|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_CP011130.1|WP_036114461.1|1385047_1387537_-|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|236528
NZ_CP011130.1|WP_057920898.1|1397828_1400879_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057920895.1|1388695_1390462_+|phosphoenolpyruvate-carboxykinase-(GTP)	gnl|CDD|235256	PRK04210, PRK04210, phosphoenolpyruvate carboxykinase (GTP).	0
NZ_CP011130.1|WP_057920892.1|1382836_1383298_+|hypothetical-protein	gnl|CDD|375655	pfam18228, CdiI_N, CdiI N-terminal domain. This is the N-terminal domain of Contact-dependent growth inhibition immunity (CdiI) proteins present in Enterobacter cloacae. CdiI proteins neutralize CdiA-CT toxins to protect toxin-producing cells from auto-inhibition. Structural homology searches reveal that Enterobacter cloacae's CdiI is most similar to the Whirly family of single-stranded DNA-binding protein.	4.04089e-32
NZ_CP011130.1|WP_148650224.1|1368165_1382835_+|putative-Ig-domain-containing-protein	gnl|CDD|225750	COG3209, RhsA, Rhs family protein [Cell envelope biogenesis, outer membrane].	1.96571e-17
NZ_CP011130.1|WP_036114493.1|1365306_1365906_-|NAD(P)H:quinone-oxidoreductase	gnl|CDD|179647	PRK03767, PRK03767, NAD(P)H:quinone oxidoreductase; Provisional.	2.16595e-138
NZ_CP011130.1|WP_057920890.1|1366869_1368030_+|MFS-transporter	gnl|CDD|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	3.26841e-81
NZ_CP011130.1|WP_036114457.1|1390696_1391284_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|236608	PRK09652, PRK09652, RNA polymerase sigma factor RpoE; Provisional.	1.87281e-38
NZ_CP011130.1|WP_082648343.1|1406207_1407152_-|Hsp33-family-molecular-chaperone-HslO	gnl|CDD|238278	cd00498, Hsp33, Heat shock protein 33 (Hsp33): Cytosolic protein that acts as a molecular chaperone under oxidative conditions. In normal (reducing) cytosolic conditions, four conserved Cys residues are coordinated by a Zn ion. Under oxidative stress (such as heat shock), the Cys are reversibly oxidized to disulfide bonds, which causes the chaperone activity to be turned on. Hsp33 is homodimeric in its functional form.	6.21916e-92
NZ_CP011130.1|WP_036114455.1|1394685_1397589_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	6.26852e-24
NZ_CP011130.1|WP_057923448.1|1407354_1408116_+|monofunctional-biosynthetic-peptidoglycan-transglycosylase	gnl|CDD|234603	PRK00056, mtgA, monofunctional biosynthetic peptidoglycan transglycosylase; Provisional.	1.22313e-130
NZ_CP011130.1|WP_057920897.1|1392098_1393052_+|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	3.41582e-20
NZ_CP011130.1|WP_082124145.1|1387932_1388616_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	4.1586e-14
NZ_CP011130.1|WP_057920894.1|1384148_1384625_-|DUF4442-domain-containing-protein	gnl|CDD|373120	pfam14539, DUF4442, Domain of unknown function (DUF4442). This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 139 and 165 amino acids in length. There is a conserved PYF sequence motif. There is a single completely conserved residue N that may be functionally important.	1.63937e-60
NZ_CP011130.1|WP_046655702.1|1401206_1404191_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	2.57907e-27
NZ_CP011130.1|WP_082648342.1|1393176_1394523_+|aspartyl/asparaginyl-beta-hydroxylase-domain-containing-protein	gnl|CDD|377460	pfam05118, Asp_Arg_Hydrox, Aspartyl/Asparaginyl beta-hydroxylase. Iron (II)/2-oxoglutarate (2-OG)-dependent oxygenases catalyze oxidative reactions in a range of metabolic processes. Proline 3-hydroxylase hydroxylates proline at position 3, the first of a 2-OG oxygenase catalyzing oxidation of a free alpha-amino acid. The structure of proline 3-hydroxylase contains the conserved motifs present in other 2-OG oxygenases including a jelly roll strand core and residues binding iron and 2-oxoglutarate, consistent with divergent evolution within the extended family. This family represent the arginine, asparagine and proline hydroxylases. The aspartyl/asparaginyl beta-hydroxylase (EC:1.14.11.16) specifically hydroxylates one aspartic or asparagine residue in certain epidermal growth factor-like domains of a number of proteins.	3.66751e-51
NZ_CP011130.1|WP_148650225.1|1391325_1392081_+|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	0.000538736
NZ_CP011130.1|WP_036114461.1|1385047_1387537_-|acyl-CoA-dehydrogenase	gnl|CDD|236528	PRK09463, fadE, acyl-CoA dehydrogenase; Reviewed.	0
NZ_CP011130.1|WP_057920898.1|1397828_1400879_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	4.06672e-24

Protein sequences

>NZ_CP011130.1|WP_057920895.1|1388695_1390462_+|phosphoenolpyruvate-carboxykinase-(GTP)
MPGSAGSLLVALNEWVAQVATLTRPDKIQWCDGSDAEHQALIAQMLADGTLESLNEATHPGSYLHRSHPDDVARVEHLTFVCTNEREDAGPNNHWMAPHEAHAKMDALFEGCMRGRTMYVIPYCMGPIDSPLARCGVEITDSPYVVANMRVMTRMGAPALARIEREGSFVRGLHSIGELDPERRFIMHFPDELAIKSFGSGYGGNALLGKKCHALRIASHQARNEGWLAEHMLIVGIENPQGETHYVAAAFPSACGKTNLAMLIPPEGYRQAGWKVWTVGDDICWMRPGADGRLYAINPEAGYFGVAPGTSTKSNPNALASIQTNTIFTNVGVTADNQPWWEGLDNGQTPVTDWRGNDYDASKGPAAHPNSRFTVSAKQCPSYSPEAENPAGVPISAIVFGGRRASLVPLVFEARDWTHGVLVGAAMGSETTAAATGAVGVMRRDPMAMKPFCGYNFADYFAHWLSFDDAGAKLPKIFHVNWFRKGDDGKFLWPGFGDNLRVIEWMIGRVKGEAGATQTPIGYLPKATDLNLDGVSLNEEAHAKLFGFDHAGWSAEFDSIGEYLGEYGPRMPQALHDEQRRIAAALKG
>NZ_CP011130.1|WP_082124145.1|1387932_1388616_+|TetR/AcrR-family-transcriptional-regulator
MNQPASNKPEPKLDTPSADLRPDGKPADRSADKPTEPAKPERSGRLSADDWAQAALDLIAEQGVAAVAVEPLARRLGVTKGSFYWHFPSRDALLVAALERWEKVEQETVFGQLEPIPDPRQRLRSLFHLVAHEVKSHVIYSELLKALDHPAVQPVIGRVSERRLDYLTASFRQAGLSRTDAQHRARLLYAAYVGFLQLNLQLHQTRMQHDEFEAYVEHMMATLIPSS
>NZ_CP011130.1|WP_036114461.1|1385047_1387537_-|acyl-CoA-dehydrogenase
MSIAIPFLAFLFIGAIAAYHRLRLPVWAALTATALVACWLLGANPTAVIVAAVIVALIAVPLMIPAIRLPFITKPLLGFYTKILPPLSETERTALEAGTVGFEGQLFSGKPDWQQLLSQPKPELSAEEQAFLDGPTEELCKMTNDWQITHVDADLSPDLWAFIKKSKFFGLNIPKEYGGLGFSALANHKVIQKLATVSSVVSSTVGVPNSLGPAELLMHYGTQEQKDHYLPRLADGREVPCFGLTGPWAGSDATSIPDFGIVTMGEWNGARVVGVKLTFDKRYITLAPVATLIGLAFRMYDPEGLIGDKRDIGITIALLPRDTAGVEVGRRHFPLNCTFQNGPIHGKEVFIPLSQLIGGEAYAGKGWQMLVECLSIGRSITLPSSGSGGAKMGAIVTGAYARIRKQFGLSVGRFEGVEEALARIAGNAFAISALSQATAAAVARGENPAVPSTIAKYHCTEMAREVAKDVMDIHGGKGIILGPKNYAGRNWQALPIMITVEGANIMTRSLMIFGQGAILCHPWVLKEMKAAMLPDKAEALREFDKNLFGHIGFAISNAVRSWWFGLTAARIGAAPGDTYTRRYYRKLNRYSATLALMADTSMLLLGGKLKFKESLSGRLGDVLSQLYIASAMLKRYEDQGRPVGDQPLLAWAFHDAVHKIELALSGALRNFPIRPVGYLLWMLIFPWGRRAQAPSDRLGHRAASLLMSPNDARDRLAEGVFLTPCENNPAGRINSYLQKVILAEPVERKFLKALKNSDIEALDFPGQLDEGVREGWITAEERKQLEELREMTIDAISVDDFDAAELRSAGYKPYAQDVNHGDSDARAAA
>NZ_CP011130.1|WP_057920894.1|1384148_1384625_-|DUF4442-domain-containing-protein
MSANVLTLYKKLTRYPAGHWLFTRAVCFKAPYFASIRPRFESLEPGRCSATMPHRRAITNHLGTVHAIAMCNLAELTGGVMTDVSIPHSMRWIPVGMSVEYLKKAVGTMRAIATPGAAIVESASGYDLPVNVEVTNPAGEPVFRATIAMRVSPKPKRD
>NZ_CP011130.1|WP_057920893.1|1383563_1383968_-|hypothetical-protein
MTATTWIHLGGLHSLAFAVFHMAFWKLFRWRDTLRSATVADRAIVQILNLRLIYVLLGIAALCFVYTDELQTTALGRALLLGMSLFWVGRTIEQFVFLRINRPMVHVLTALFVLGALIFVMPLLPATCLHTECE
>NZ_CP011130.1|WP_057920892.1|1382836_1383298_+|hypothetical-protein
MSGFSLFLGLEPSDEDGVACLQGRIQVGEFTEPLLCPIGYWARQDYVEQWLHALDQICMGKEKTALIVSIYDPESSNFVMVWPLYLIGDNVHVQNSIIFLEHLDEVFDAGKVGMYVEDHATISDEGEKISEWIVPVEAIRKALLRGVVTETVT
>NZ_CP011130.1|WP_148650224.1|1368165_1382835_+|putative-Ig-domain-containing-protein
MAAVISGNGLGLFNSSASQIGMGLGGGARLGQGQDHQFVNVATGNLLLQSQDDQVLFRGMLVGFNRTYNSRGQLSQVGADAWLTGFERRVELLSGTFNIAGSVMRRHTGDGSYQDFTFVSAGVYSSSTGEGAHDRLSWDAGSSTWSYVEGSTRQEERYADHASATLKGRLTQLRDLRTDGAQPLAWDVSYDANGRVSQVAAQQGDQTRFVFAYDSGGRLASVTSMSGAATLGQTFYAYDNAGRLASVTLDLTPGVVVDGLGTPDHNQWTAAAGSNDGYLFKTTYTYTDATSLLISRVEQSDGTVTSYTYDAQNRIKTVTRGDTNSNDADGFGQTLSFSYDSPTTTSMADSAGRMWTYVYDASGQLTEVRQPAVDGVRETTSYTYDAAGNVTRVLTKYSGLVLSQTDYAYDANGNVTWQWDRAQSGSNATSRAVQRTYTAGNQLASETEYTGLDTDGLAAGAAPSGGLTTNYLYDAQNRLRYVIDATGAVREQEYYTSGTGIGQISKSRRYLGDAYTGAMTLSALESWSTTARKASSILTDYTHLSVQARSERTYANVDASGNGIASDADVLEGYRYDERGRLTLKNYASAINSFRTVYVYDGMGRLTSEWVEENQIKVRSATWVYQDSQRLSHAIIEGGVVGDNDQSNDRIRTEQRDAAGQLIYIKESALSGTASGVRESRNYYDNTGRLRASEDSGGARTYFFYDLEGQLSGQVDETGAVTEYLRDQLGRITSTKRYATRANPTHWQAGESPEENPGDPGPGDPGPGDPGGGPISMSAQSTGNIRTGWLVGNIFVYDLIEDARPADSVDDRSTSTSYDALGRVVTQTDAEGAITTYSYDGANRLLQTRTTDAAGTAATARVVRYFYDAQGRETGRLDAEGYLTEHSYDLAGRRIRSVAYATVTPAAQQASGALNDLRPASSTNDQTTRWFYDGRGNLVATLSAEGYLTEFVHDAQRLQKATKAYALKLGGLSGNESLATLRTSAAAGGVRETRLSYDSAGRIIVEQNPEGTVTRYTYDAQGNLIRSEVAADTTEVREGRMRYNVFGELIGELHGEGAARVLPGMSEAQLDALYAQYGVRHSYNSLGQRSESIDAAGNKTWYFYDASGRPTFVVKGVADASGVANAQGEVIETRYNAFGEAIETTAYTGRITLATAGSRDSVASAITTLAYVAASDSRRSVSYNHRGQVVGSVNAENAATRYTYNAFGERIREVSAFGAPTALTIETDYDRRGLATARREGVGSAVARAHGWTYDAFGRVTTAVDARGIATTYSYDRLGRQLTASQTVMGRQELVSTSYDAFGRVLSITDALGRTTTSAYDTTNRTTTVTTPEGVSVTTTFNRHGQQVNVATPLPGGTVANTSYLYDRDGNLKSTTDALGRADSNEYDARGLLSATVDRTGRRVELRYDAVGRLLQRIEDPAGLALTTTYRYDGQGRQSEVTDATGRKTAYSYDREGRLTQVAADPAGLNLRTAYTYDALGRQITVTEGAGTAQARTIQYDYDALGRRIAERLDPAGLNLITSYAYDANDNVVRRTDATGNVARFYYDEADRMIYTIDPLGVMTRNWFDVTGKVVATRTFIAATNASTLTDTTTIAQLDARLAWGSTDPGSYTVYDRDGRARLVLSTIGTIQEFTYDAAGRVSVIRNYAALWPDFGTTMLNKLFAGTAQLSDFNLDALRNDAATDRARDLVTYQVFTVLGELRTTVDNAGTVISYVYDAAGRQTVHKRYAHAAQLNPTLRAKLVAGRASPQDVVDVVAVFNETDLVTYTSYDGAGRARYTVDGNGSVVEILYDSAGRPVGTRAYATAIVVNTDATFKAQLIAGDPAAMGMVRDRVAAIANDARDLRSYQVYDSAGRIAATIDGAGYVSTRSYDAAGRVVQERRHAQVATIAAPLLAKLVAGTASVADITAVTPVNNAADAVVRHIYDAAGRERYTLTQNSASTYLVNERRYDGAGRVTAQYQYAVPIALGPVATPADVGTALNAAGAYATADLYRSTQYVFDAAGRVRFTVDDLGAVNEQRFDGAGRVIETRRYGGYISISTPMNDAAVSAAVAAIVEVRTTTTTYDAMGRVLRVTDALNQYEEYTYNPLGQVTALRNKNGHVWNYEYDAAGRRTAEISPQVWIANVDAAGTQSYGVRRVVTRTEYDALGNVTRRLEDADGARARITRYEYDNRGNQIRTIFPDAGKIDPANGQLIASGIQPTIEITYDALGRAVAQKDVRGNYSYKVYDNLGRLAYDVDQENYVTAYGYDGFGQQTNLRRHAQALNVGALAGWAPGQPLSMAQMQAAAAASASDRTIATRYDQRGLAVQIEQAQIAYYTSTGAAATGSPTVRIEYDGFGNKVKESILLEGTAGQADARWADTYTYYDLVGRVTMTVDAEGYVTRARYNATGEVVESIEYARAVWTGGLNTAAPPALPSAGDEIIGYDRITRLSYDALGRKISESAVRHFQRSDGSSGVRDVVTQFRHDGADRVTQIINDAGTTSTEYDALGRAVSVTEPTRKVINDGTFGILAQNTGYDLNHPDVYADASPYTGMIYDAFGNLVLTRRFASGKNAAGQVVEDGNKDQIERVRYDWQGRAVATSASNGDTAYTDYDAADSVTHRWYVLSGTQANRDVRVHSWYSYDKAGRQTGVGQTRDLLNGGGSSTDLSEAVVYNAFGEIVQKTYAGLTGSLNYVYDAAGRLVTSNENFGARNFGYNLAGHQVRESHVVVISDGQTGGGRQSVDATTFNTTDRLGRTTATRLPSNTTDPNATLSVQQRLDRWGNVLQVIDARGYQTNYRYNESSQVTRDERPLVEVVSENGQSSWLRPVNYWFYDALGRLVGTRDANGNTRTNQYDAAGRMISSKDALGQATLFAYDALGNQRITQNPLGYLTYKDYDNLGRLVEIGDYLPAAGASNRVRTALQHYWLNQNGDRIVVADALNQQARYDYDSRHLLINSQSATGVSNSYAYDVMGHKIRESNGLSGGAIVDRDGETVSNNELTWDYDAYGRLIDHNNLSGRDFDYAYDPITGQLTAESQSGGAAAYAYRYTTYYADGRVKAVHENGAAPTYRYEYDAAGNRTLEEASIVEGGGQYVHTVTRTWYDSHNRIQRVVQDDLASGSAKRVFDLSYRYDAAGNRRNVKATSGYGPNVDGIAVVNQSPTVAQTPAARSVRRGMSSEFAILFSDVFRDAENDAMTLQITLADGSPLPSWLTVSRDAATGVIRFVAQPAANAPNQDLSIRLFAYETADSSKNATAVFTLYVRENVGPQLLNGNVETLRVKTGQAWNKDLLVTDFFYDLDVGDRMRLTLDNAGSLPAWMQLDTSSPGAIRITGVAQTGTYTLQLRATDEAGWSVVKTVQIVAAPNSAPTGPAPLPTSTAVVGRQFNWSIPIADAFYDADGDSLEIVASGLPSWLTFQRTVVQGQPQLRLTGRAPDTAPQPAYQIAFTATDPDGASRTTTMTLTMRTYNNDPTAPSSIAVPFAVVNFPGYQYQLPAFTDLDGDAITYSLRDLPAGMTFNAATRTISGTPTQLSSGWVTYVGEDAYGGIAMTGFYLHVRGNTAPVASGIPNQSAGVGISWSYDIPRFSDAEWDALTYTATGLPPGLWMNTDGRIVGTPNAAGSYGVTVYGADPYGGSASTYFVITVNAAPPPNRAPQINPARPIPGAEFTSTNRWPTPYQDFGFAVDTFIDPDGNPLTYSFVELPGWLSYSYSAQYGHILGGYPPGQTITERIIMRAQDNSGAYVDMTFYVHTTYDHFDPGNPTDPLSLPNPVSVVASDANTFAMGAPAALDDGAESSLETMQAAATASVATASSGTIPTQTKEFWFTYDAENRIKINNGQLLNGQIQLVSYGEDSYELMYDAAGHEVARVNLRPGYPSGQSVWIERSAFDLRGNRTVEYWEEVVQGASVSNEGIRKVLSYDANNRLIETRSFFGASAYWDHTSRPGEQYEFYNRYEYGGWLWKAEQYAYDADGRLMYQQMLERNMSQEDWVMRASGNQTTNLGVLDFDSRTDYRRTDNDGSATGFDAANRLMTYRYITTRYTHTYDSTYQGWESYQENTVSGRSSDDTHYRATTNTLVYDGFGRLKSQRENTPLSNGSIDDRIRYYGYNGDGSVQTRREGSLNGSGQFIQDTQYGPGNYLLVHAAGQQQAELKQGYQYVYNGATINSKQIVSLNGRGNYTAGGNTVSAQAGDTLRSVAKRVYGTDQLWYLLADANGLGDPDQVLFAGTQLVAPNTKVSSNDANTFKPYNPADAIGSTTPNLPYIPPPPKAGCSTLAMVIMVVVAIVVTIYTAGAAAGAMGSAATATTATVGTTVAGTTVTAGMAAGTLTTGFAATMSVGASALAGGFGMAAAVVGGAVGGLVGSIASQAIGSAMGATSFSWRAALVSGAVGGATAGFGAAAKAGQLGKLLADSQYLRAGATAVVGQATSYAASKAIGLEASFSWKSVAASAISAMATTKIGGVPIAEGGTSTGDLINDFAGGLLRGAIDGTARRLMGGGRQDWASIAADAFGNALGNAAVRGLEAWQADRAIRDVAKQHGIEFAGRNRNGEYFTRAGVVDAFGKPMFDAEGNPITTEGYSTYRSIKEMLAGGATLDQIHGAVGDDRFGSLMQQTDSTEYFASHLRFAEVGSIEILSGDPGQPSVEAPKDPPSLAQTPEVGEESRGVAIQLMGGLTSAGAKLADFNEAHPWMTSLGVNVAQAALTGGPTKTVVLNIAKGAAGEALDQHVIGPIRDKVRTGVSGFLHDTVGLAETPSNILAEGVVFGADLFAGSAAQAIGTGTNIRRMTNSSAEWNTSGWLRDRHAGSPSPALKGDPYHPDSVEARRAEFRALYGSFDPKVVAHELGYTRRIPPQKAPFKSHGQSVFFNGKQYITPDVDGHNVANGWKTFDLKGRRTGTWSSDLSVRIKD
>NZ_CP011130.1|WP_057920890.1|1366869_1368030_+|MFS-transporter
MLLPIILLSAAGFTVLTTEFILVGLLPSLARDLDVSVSQAGLLVTLFAFAVAASGPFLTAYFSRFERKRLFIVVLLLFAASNLIAAIAPNLGVLAFARVIPALGVPVFWALASETAVDLVGQERAGRAISVISFGVICATVIGVPTGTLIADAFGWRAAFVALAIASLLKATLLFVFLPDSRADKPQMKLLEQFQVLRDPRVSGHVLLSILLFTGMFTAYTYLADLFERLAGFDGSVVGWALMAFGAVGLIGNTLGGRIVDRNPLAASLIFSVPMALGLVLVVPAIQSLPLFALTLALWGITQAALFPVSHVRVMKSAPQAPAFAASLNISGANLGIGVGAMVGGRVIDAIGIGGVGYVAAGIVAASVLLGFVLMSAGERAEPEVV
>NZ_CP011130.1|WP_148650223.1|1366076_1366346_-|hypothetical-protein
MDVSQPDEPRPRARPERIPYFFLAALSMLFLQRTAKLWNGTFFGPSLYDELAIAGAILAAISLVLRERAWLLSIMLLAVNLFILSLKFW
>NZ_CP011130.1|WP_036114493.1|1365306_1365906_-|NAD(P)H:quinone-oxidoreductase
MAKVLVLYYSAYGHCEKMAEAVAEGAREAGAQVDIKRVPELVPEDVARKSHYKLDQAAPIAQIGDLEHYDAIVIGTGTRFGRMSSQMANFLDQAGGLWAKGALHGKVGAAFTSTATQHGGQETTLFSIITNLLHFGMVVVGLNYGYAGQMRLDEVTGGAPYGATTITGGDGSRQPSQNELDAARYQGREVAETAKKLHG
>NZ_CP011130.1|WP_036114457.1|1390696_1391284_+|sigma-70-family-RNA-polymerase-sigma-factor
MLTAVNESLADATVSPEAEDDRALVAAAAAGGVAAFEALYRRHASRVHGVIARLVGYHGARAEDLTQEAFVRAWQALPNFRFESAFGTWLHRLAVNTALMELRGRRSRPLEDSDEDAFDGIGSADSAGHVTALSMDLERAVASLPPRARAVLVLYDVEGWKHEEIAVELGMAVGSSKAQLHRARSLLRTRLGEQA
>NZ_CP011130.1|WP_148650225.1|1391325_1392081_+|hypothetical-protein
MPDALRWQLRALRRDTPPARDLWSGIAARLGEQASPQDEPAPVDHLAPIVAAPGDASPAEAAPIEAAPAPQVIVLRARESSRPRWLAPMALAASVAVLAVALGVMWKGGAAVDGTAAGDVAAAGGAAGQDSSASTAAGIADAGTKPVDGRAVAQNSSAPTDTGIAHAGTTPASLVQREADGMTRQYQAAMREIEPVSQQAVALKPAFDELDRNTALILDAMAHDPDSRLLLEQLRRTYARRLALAQRVAYT
>NZ_CP011130.1|WP_057920897.1|1392098_1393052_+|DUF4097-family-beta-strand-repeat-protein
MIHSRSRTTSRVLRRLPAVGLLALGLAVALPAFAATPINQSRPIDPLGSVEIDNVKGLIQVRAWDRPEVKIEGSLGEGVEKLEIEGDRENLSIKVRYPNRGSGMGLLAGGDKGEPTELRVTVPLRVKLEIDAVSADVDVSGVASRELSIDSVSGDVVVAGAPREAEIDSVSGDLRLTLNSGKVSAQTVSGDLELRGRLNGEVSVETVSGKVDVATRESSLNKLSGNSVSGDLRVAAALADGGEASLETVSGDIRLTLPRSLSANVRGQSFSGDLRAPDAQIQRPKHGPGSSFEHRYGSGSGKIKLETFSGDATLELN
>NZ_CP011130.1|WP_082648342.1|1393176_1394523_+|aspartyl/asparaginyl-beta-hydroxylase-domain-containing-protein
MPRPLRKHRSDGRQGRGRDIQPGEDAVLNEQVNQLVQAAGLASRAGRWQEAEKLWQQVRAIAPQHPQALYSLGIHAFQQGDTQGAIELLHAAHRSAPNDPMILLSIGVVQRERGNSAAEWEAISASLAADPYFLAGLLAKASFFERSGKPRAAADAYRNALTVAPPQPHWPDMLKEQLLHASRRVEAYREEFAEFLAHRVGGPRAALDVGTLGRWDEAASIMVGRSKPYHADCNQLCVPRLPAIPFHDRSQFAWVEELESRTYDIIKEMRVVLREEQAEFTPYIEYQPGDPVNQWRELNHSRRWSTYKLWSYSKPVDEHLARCPQTRAALEAVEMAAIADVCPNAMFSALAPHTHIPPHHGETNARLVVHLPLIVPDNCRYRVGFERREWKVGEVLIFDDSIEHEAHNDSDELRVVLIFDVWNPLLSLAEREMVNAMMRAHRDFLAGR
>NZ_CP011130.1|WP_036114455.1|1394685_1397589_-|TonB-dependent-receptor
MTLKTTQLRDAIVFALCVGATSLAGTGLASAQDASAPAAAPAEADATTLDRIQVTGSRISIPGLTTNSPIMTVDREEIARNQPVTAEDFLKIVPGAVPSIGPGTNNGANGGATINLRGLGDNRTVVLMDGRRVVPFNLFGVVDTNVIPVALIDSVDLVTGGASAVYGADAVAGVVNFVLKRNFEGVEVNTSYGQSSKQDGDRRNTTVTLGMNLDDGRGNFVISLGKTDNDPLLQGARGFSEFNLDSTNGEAGGSGTSIPTRVGPLGQINPTTGRFDGIVTPFNYNPFNFNQTALDRWQATALGRYEINEHAEAYTQVLYTRSNVFSQIAPGGLFGGRFDLGIGNPLIPDAARQQMCAQFGVAAGDCVVGSSATVNTTLNRRTTELGTRSTDFQNKVFQATLGLRGAINDRWRYDAYWSHGEADQLTVSAGFLSKARTQQALLSTDGINCVNPANGCTPINLWGPEGSISKDSKKFLEVLTFATQRVEQEVWSGSVNGDLGDNFKSPWADYPIGLAFGLEGRKMTAQNRADAASRDPEEVQGSGGANPDVEGAFTLREAYVETIVPLISGKTGAHALNFEAGYRHSQFKSGQTDTDYGSYKYGLEWAPIESLRFRGMFQRATRAPNINELFQPVVTGLDNTAVDPCEASQLALNGGITGDVAALCVATGVPQAILNSQGGVDGPSAGQANAFVGGNPILGPEKADTQTLGLVWQPMEDFSITLDYWKIDIKDAITRPVLGDALFGCYDRQFNPTLSLSHPMCQLMVGAREAVDGSLNGEARGPFLNRSNKGRIVTDGWDLGVRYGIPLSNDWGRLDFALDLTKTSKYDYQGDPQVETHDCVGVYGVSCNVIAGIVYDYKSNFRAVWSIKDFELGFNWRHLSAVDVEDGPIEWFPAYTSIDAYDYFDLTMAYELPWNARINLTVNNIADKKPPVVGSNIGSTGFNSGNTFPQYYDTLGRYYTLGLTMRF
>NZ_CP011130.1|WP_057920898.1|1397828_1400879_-|TonB-dependent-receptor
MILKTNQLRDAITFALAVSSTALVGTGAAFAQETGSKEATTLDRVEVTGSRIRQVDVETAAPVLQISRAEIEKQGYKSVADILQNITAAGSPAISRTSPLSSGESVGGYYIDLRNLGANRTLVLVNGKRLGATNDGLQDVSSIPSGMVERIEVLKDGASTIYGSDAIAGVINIITRKNFEGAEANAYIGQWGQGDGTRQSYDFTIGFTGDRGSVTVGAEYSKEDPVWARDRWFSQAGAPTGPKSEPRDFVFSGTTQWGALLAPVGRNAAGNPVDAWTGLRATGPTNPASGLPVSAPRFLARENAGLDLRDSRNFRARNGSDVSLPSSQSTVYSGIERKSLFVNAGYDITDWLRFDTDIQYNDRDSFAQNAGYPFQSAVLAPGFNTPLSIDSYYNPLGNQRTGPLPPFLTAPTAVHFVRRGWEVPRQVRNSLTTYRFTGAFSGSFELGEGKIWDWDAGYLLNENKATQISTGNLNVANVRRAVGPSFLNAQGQVQCGTQANPIALGVGGGQCTPWNPLLPFGYAGANGLNDPNVQKYLYQNGQAVGKTKTTDYFVNFSGTLATLPAGDLSLAVGYEHRKEQGNFSPDALSQTGGSTDLASGPTGGSYSLDEFYGELQIPILADMTGAKELTVNLATRYSDYDTFGDTVNSKFGVKWKPIDSLLVRATYAEGFRAPTISDLYGGLSQSFSFYTDPCDTLFGNSGGSAACVGNSDPRLRVPANFRQPANTATGLAPRPSTQTGTPFLSGSNDQLVPETSTSKTFGIVWSPGFVENLNLSLDWWNIKIENAITGDSPSQVLADCYTRGITSRCNVEQDPSRSRFTRDPVTGGVNSFIFAPINVGYNEVEGFDFDVNYRIDTQWGRFGLAWLSSYTVKNELQTDVLGEAVPSQQNGFGGFFRLRSNLNLSWDKGPWGFTWGMRYYSGVKENCSFDDRCSLPDYTAPEFNGANTPMNEIGSNTFHDMQVRFNAPWNATIAVGANNVFEHYSAPNYDNPNSGYAYYGGYDIGRFIYFKYQQRF
>NZ_CP011130.1|WP_046655702.1|1401206_1404191_-|TonB-dependent-receptor
MTFKTTQLREAISFALAVGTTALVGTGIASAQDTAGSKDATTLDRVEVTGSRIRQVDVETAAPVLQITRADIEKQGFKSVADILQNITAAGSPAISRTSPLSSGESVGGYYIDLRNLGPNRTLVLVNGKRLGATNDGLQDVSSIPSGMVERIEVLKDGASTIYGSDAIAGVINIITRKNFEGAEANAYIGQWGQGDGTRQNYDFTIGFTGDRGSVTIGAEYAKEDPVWARDRWFSQALFPTGEKSEPRDFGFSGTTQWGALLIPTGATLPNGTPQMGAPRFLARETPGLDPRNIANFRARNGSDVSLPSSQSTVYSGIERKSLFVNAGYDITDWLRFDTDIQYNDRDSFAQNAGYPFQSAVLSPGFNTPMSVDSYFNPVGNQAVANGTMPAGQAPTFVHFVRRGWEVPRQVRNSLTSYRFTGTFSGSFELGEGKIWDWDAGYLYNENKATQISTGNLNVANVRRAVGPSFLNAQGQVQCGTAANPIALGVGGGQCTPWNPLLPFGYAGTNGLNDPNVQKYLYQNGQALGKTKTTDYFVNFSGTLATLPAGDLSLAVGYEHRKEQGNFSPDAISQTGGSTDLASGPTGGSYTLDEFYGELQIPILADMPGAKELTVNLATRYSDYDTFGDTVNSKFGVKWKPIDSLLVRATYAEGFRAPTIADLYGGLGQSFSFYTDACDTLFGDAAGNARCLQNVPAGFRQLANTASGLAPGPGTQTNTPFLSGSNDQLVPETSTSKTFGVVWSPGFVENLNLSLDWWSIKIENAITGDSPTRVLADCYTRGIESRCNTGQDPARSRFTRDPVTGAITSFIFAPINVGYNEVEGFDFDVNYRLDTQWGRFGFAWLNSYTSKNELQTDILGEGAPSQQNGFGGFFRLRSNLNMSWDKGPWGFTWGLRYYSGVKEECYFDDRCSLPNYMAPDTNGQVSPKNEIGSNTFHDMQVRFNAPWNATIAVGANNVFEHYAAPQYDQPNSGYSYYGGYDIGRFVYFKYQQRF
>NZ_CP011130.1|WP_187313401.1|1405214_1406030_-|hypothetical-protein
MLALGVATGAHAQTKRDTTYLPVWNQNNGKLEYVLQLEPAEKQAAGARWKSGANTFDATLGLDGGDGLGLVCDRKTGLAGAIGNLANHCLLAALDEDDDHANNRQLSAGASLSRPGGKVGVAIGSGRDALPGWLSPNNRNSRVDQNTLTVYGQKNIGREAMVSIGGTWARAKLIPAGEMPGLADRWSSKSITIGAGIGNFGANIVGRVVDTPGQPGQWEGLGVGLTWRTPWSGQLTVGAENVVTRGKNPFAPGNGEKDEGTVPYVRYEQDL
>NZ_CP011130.1|WP_082648343.1|1406207_1407152_-|Hsp33-family-molecular-chaperone-HslO
MTDAHPAATTASGADTAGETDRLTRFMIETAGVRGVHVHLHETWRQIRERAEYPAAAAQLLGEAVAAAALFTGHAKVDGRLSVQLRGNGALRTLFAECTAAGTLRGIVQLSEDGGEVSRDLRELGPDAMLAITIENPGLHGRDPVRYQGLVGLESDSLAGAFEGYFRQSEQLPTRLLLVADEHRAAGLMLQKLPGDEGDDDGWIRAGALFDTLRSDELLSLPAATVLNRLFHEDGVQLLGDKPLAFACSCSRERVEAMLVSLGREEADAAVDAADGEAHIRCEFCGQRYGFDRNQIADLFAAAAAQMQAPQRVQ
>NZ_CP011130.1|WP_057923448.1|1407354_1408116_+|monofunctional-biosynthetic-peptidoglycan-transglycosylase
MPGPGPFDVANGPGQSAPRPRRLRRWLRWLIALPFLFVLASILQVASLRFIDPPFSAFMMIRQFEAWGSGDFGFRLAHDWRDLDEISPNLPVALVASEDQNFAEHFGFDLKAIEKARKNNERGRKVRGGSTISQQTAKNLFLWSGRSWIRKGIEAWYTLLLETMWPKHRIIEVYANIAEFGDGVYGAQAAARTFYRKDASQLAPAEAARMAAVLPNPKRYSIARPGPYVQRRAGAIQRQMRYIGGSEYLKQLE

Crispr_ID: NZ_CP011130_8

• CRISPR_ID: NZ_CP011130_8
• CRISPR_location: 1954797-1954898
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_8

Consensus_repeat	Method
CTCTCACTCACTTCTCACTCCTCTC	CRISPRCasFinder

spacers of NZ_CP011130_8

>8.1|1954822|52|NZ_CP011130|CRISPRCasFinder
TACTCGTTCCTGCCCCGCCGGGGAGTGGAAACGAGTAAAGGCCGCTCCTCGC

CRISPR arrays and Neighbor proteins around NZ_CP011130_8

CRISPR arrays

The CRISPR arrays of NZ_CP011130_8

>merge|NZ_CP011130|8|1954797-1954898|CRISPRCasFinder
CTCTCACTCACTTCTCACTCCTCTCTACTCGTTCCTGCCCCGCCGGGGAGTGGAAACGAGTAAAGGCCGCTCCTCGCCTCTCACTCACTCCTCACTCCTCTC

>NZ_CP011130|8|7|1954797-1954898|CRISPRCasFinder
CTCTCACTCACTTCTCACTCCTCTC	TACTCGTTCCTGCCCCGCCGGGGAGTGGAAACGAGTAAAGGCCGCTCCTCGC
CTCTCACTCACTCCTCACTCCTCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_036114799.1|1941223_1942591_-|ATP-binding-protein	unknown	unknown	gnl|CDD|223540
NZ_CP011130.1|WP_057921189.1|1944412_1946272_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057921188.1|1943992_1944409_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046658894.1|1949268_1951281_-|M13-family-metallopeptidase	unknown	unknown	gnl|CDD|341056
NZ_CP011130.1|WP_057921193.1|1958976_1959393_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036114778.1|1942853_1943996_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|184118
NZ_CP011130.1|WP_057921194.1|1961364_1961880_-|DUF3304-domain-containing-protein	unknown	unknown	gnl|CDD|371700
NZ_CP011130.1|WP_036114746.1|1965769_1966666_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213231
NZ_CP011130.1|WP_187313365.1|1964567_1965437_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_CP011130.1|WP_036114782.1|1940747_1941224_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057921187.1|1939824_1940751_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|274350
NZ_CP011130.1|WP_057921196.1|1963175_1963460_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923484.1|1959456_1961001_-|BCCT-family-transporter	unknown	unknown	gnl|CDD|376718
NZ_CP011130.1|WP_057921192.1|1957436_1958810_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|224157
NZ_CP011130.1|WP_187313364.1|1951781_1952222_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_187313403.1|1954912_1956997_-|peptidase	unknown	unknown	gnl|CDD|226118
NZ_CP011130.1|WP_148650273.1|1946264_1949033_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057921195.1|1961961_1963161_-|low-temperature-requirement-protein-A	unknown	unknown	gnl|CDD|226742
NZ_CP011130.1|WP_082124209.1|1952449_1954588_-|peptidase	unknown	unknown	gnl|CDD|226118
NZ_CP011130.1|WP_057921197.1|1963633_1964407_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|183716

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_036114799.1|1941223_1942591_-|ATP-binding-protein	gnl|CDD|223540	COG0464, SpoVK, ATPases of the AAA+ class [Posttranslational modification, protein turnover, chaperones].	3.19429e-74
NZ_CP011130.1|WP_187313365.1|1964567_1965437_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	5.46874e-26
NZ_CP011130.1|WP_046658894.1|1949268_1951281_-|M13-family-metallopeptidase	gnl|CDD|341056	cd08662, M13, Peptidase family M13 includes neprilysin and endothelin-converting enzyme I. The M13 family of metallopeptidases includes neprilysin (neutral endopeptidase, NEP, enkephalinase, CD10, CALLA, EC 3.4.24.11), endothelin-converting enzyme I (ECE-1, EC 3.4.24.71), erythrocyte surface antigen KELL (ECE-3), phosphate-regulating gene on the X chromosome (PHEX), soluble secreted endopeptidase (SEP), and damage-induced neuronal endopeptidase (DINE)/X-converting enzyme (XCE). Proteins in this family fulfill a broad range of physiological roles due to the greater variation in the active site's S2' subsite allowing substrate specificity. NEP is expressed in a variety of tissues including kidney and brain, and is involved in many physiological and pathological processes, including blood pressure and inflammatory response. It degrades a wide array of substrates such as substance P, enkephalins, cholecystokinin, neurotensin and somatostatin. It is an important enzyme in the regulation of amyloid-beta (Abeta) protein that forms amyloid plaques that are associated with Alzeimers disease (AD). ECE-1 catalyzes the final rate-limiting step in the biosynthesis of endothelins via post-translational conversion of the biologically inactive big endothelins. Like NEP, it also hydrolyzes bradykinin, substance P, neurotensin, and Abeta. Endothelin-1 overproduction has been implicated in various diseases including stroke, asthma, hypertension, and cardiac and renal failure. Kell is a homolog of NEP and constitutes a major antigen on human erythrocytes; it preferentially cleaves big endothelin-3 to produce bioactive endothelin-3, but is also known to cleave substance P and neurokinin A. PHEX forms a complex interaction with fibroblast growth factor 23 (FGF23) and matrix extracellular phosphoglycoprotein, causing bone mineralization. A loss-of-function mutation in PHEX disrupts this interaction leading to hypophosphatemic rickets; X-linked hypophosphatemic (XLH) rickets is the most common form of metabolic rickets. ECEL1 is a brain metalloprotease which plays a critical role in the nervous regulation of the respiratory system, while DINE is abundantly expressed in the hypothalamus and its expression responds to nerve injury. A majority of these M13 proteases are prime therapeutic targets for selective inhibition.	3.41389e-161
NZ_CP011130.1|WP_036114778.1|1942853_1943996_+|AAA-family-ATPase	gnl|CDD|184118	PRK13531, PRK13531, regulatory ATPase RavA; Provisional.	9.23367e-42
NZ_CP011130.1|WP_057921197.1|1963633_1964407_-|SDR-family-oxidoreductase	gnl|CDD|183716	PRK12744, PRK12744, SDR family oxidoreductase.	3.52066e-151
NZ_CP011130.1|WP_036114746.1|1965769_1966666_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213231	cd03264, ABC_drug_resistance_like, ABC-type multidrug transport system, ATPase component. The biological function of this family is not well characterized, but display ABC domains similar to members of ABCA subfamily. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	1.16267e-103
NZ_CP011130.1|WP_057921187.1|1939824_1940751_-|tetratricopeptide-repeat-protein	gnl|CDD|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	1.19635e-14
NZ_CP011130.1|WP_057923484.1|1959456_1961001_-|BCCT-family-transporter	gnl|CDD|376718	pfam02028, BCCT, BCCT, betaine/carnitine/choline family transporter.	0
NZ_CP011130.1|WP_057921192.1|1957436_1958810_+|MBL-fold-metallo-hydrolase	gnl|CDD|224157	COG1236, YSH1, Predicted exonuclease of the beta-lactamase fold involved in RNA processing [Translation, ribosomal structure and biogenesis].	1.0439e-102
NZ_CP011130.1|WP_187313403.1|1954912_1956997_-|peptidase	gnl|CDD|226118	COG3590, PepO, Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP011130.1|WP_057921195.1|1961961_1963161_-|low-temperature-requirement-protein-A	gnl|CDD|226742	COG4292, COG4292, Predicted membrane protein [Function unknown].	1.81713e-107
NZ_CP011130.1|WP_082124209.1|1952449_1954588_-|peptidase	gnl|CDD|226118	COG3590, PepO, Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP011130.1|WP_057921194.1|1961364_1961880_-|DUF3304-domain-containing-protein	gnl|CDD|371700	pfam11745, DUF3304, Protein of unknown function (DUF3304). This is a family of bacterial proteins of unknown function.	7.71226e-25

Protein sequences

>NZ_CP011130.1|WP_082124209.1|1952449_1954588_-|peptidase
MPSRLEPAVTFKKPQVLLLSLAIATVVAACGKTEAPAPTAPADTTAAAAPAEATLKLDESKLPPVNRFLATDLDTTKDACTDFGGYVNGKWLAANTIPNDRTSWGAFEMLDERSNAVQRQLAEQAAADTKATGVEKIVGDLWATGMDVAKVNAQGLEPLKPDLAKIDAIDSPEKIAAYLRDAAATGDNNLFGFGAEADFKDSANNIAYASQGGLGLPDTTYYTDAKHKDKLAAYEVHVAKVLELGGAKPEDAAKQAKDVIAFETRLAKASKSREQLSRDVSLYYNPVSPAQADELTPNFSWTKFFESQKVALPAKFSLAVPAFHQEVSKMIGELPAAQWQAYLRFHAIDGASPYLSEAFVNESFNFYNKTLRGQKELKERGKRVLDTIEGQTGEAMGQLYVKVAFTPESKERMQALVKNLSEALKARIENLSWMSADTKKKALEKWASFTPKIGYPDKWRDWSGLSTGRDSYYANVKAANEFNYKWNLSKIGKPVDKTEWGMPPQMVNAYYNPLQNEIVFPAAILQPPFFDPKADDATNYGGIGAVIGHEMTHGYDDQGSRFGPTGNMEVWWAPSDAKAFSGLTDKLIKQFDGYEAAPGAHVSGKHTLGENIADLGGLATAYDAMKKAAGDTPDPKTDGFTREQRFFLNWGTVWRRNFTPEELKVRLQTDEHAPANFRAIGAPSNLPAFAAAFSCKPGQPMVREGDKQVVIW
>NZ_CP011130.1|WP_187313364.1|1951781_1952222_+|hypothetical-protein
MTPDYKTGEQALDAAIRAYPWMDFHLVAYDEVSLIVRGTLDLSYGYQLQIEFGDVGYLDCPMTWRTATHAQVFSKVDPVTLRDDARERFFDGNGGEVFRFAVEGVHRPWFAHVVAARMRFFAAAHGEYLNWSDQAGAFDSRCRAGR
>NZ_CP011130.1|WP_046658894.1|1949268_1951281_-|M13-family-metallopeptidase
MSTLRPLVCALTLSLIAGLASPAADAAKKKAAAKPKAPAAANACSDFYANANADWLRANPLSGAASVSSLETLTANARRQQLELLNSAMTAPQGNVQKLLGDFWASGLDEAAVERDGSQPIAPLLGRINAIKKAKEIPASIAALHQVGIPVLFNFGADIDLQDLDRHIGYFSQGGLGLPDPAYYTRSDADTRQLLGHYNNYVQKILTLTGTPKEKLAAESLQVIDLETRIARASKALPDLRDPRANYAPVQVATLAKTYKGLQLADFLKAQGVSDDSVSLANPQLFAELDKLLGSLKPDQWKTYLRWRVGDSMAPYLAKPFRDAEFDFRGKVLRGQREQPARQQAVLDAITLAAGPMVGHEYAARYLPAATDARAEQIASQVREALGKDVEADTRFSEAVKNEAKAKLAKLKIEVGTPKRDLDYTVQPMGRGSFGSNMLIASTWRHREEMKRIGRGNADRRWDVLPQEPSLAYDIAQNRLIVTAAMLQAPVLDMSKPEAAQYGSYGALVGAELTHGIDGRGRYVNAKQEVRDWWTPTEVAAWEALGSRVAAQYSAEPYPGLTATKINGAQVREVAIADQAGVELAWSALHAAQPAASKDANQAFFRAWAGLWAQQLSPEVAAQRAATGIHAPGPARTNVPLSNLPAFGEAFGCKAGTAMQRKADQQIKIF
>NZ_CP011130.1|WP_148650273.1|1946264_1949033_+|hypothetical-protein
MSDRTTPADATVRHPVWRGRQTVDGLWLAADWLSPERRSERVLREWMPGCRAWRFEHGDVLCFEAPRMLQCEFAGGTPLRRVGAHGLYAGPLTEEERAALAAGDVHLVIGGQLQSLHFAKAQTLDPSLVIDIDDYALHDTYDGRRSLALPKAGRLTGKPLREVLGDKIPPPSQEREAFLRDAAARGAGKDAGGKPIGLGLSSAKPSLRERAVGTRDRMADWLLQRFPGLSGDASSGRGGVATSGRGAGTGGGSVRPRNRAIVPQRWRDMLVRFAIASRASRLIGMRHGAYLRRLMEQFDRGDLNEALRNALPIDGSGDSLGQAFSAPGRRDSLRLSQGNGAATSIDFGDSARDRLRKLYRNAFEQLDRQGKIDEAVFVLAELLNARNEALDYLVKHERFAQAAELALSWDMAPDLIIRLLMLAGDRERAVLVARRDNAFAAAVALLENGHPRQARQLRGEWGQALAEQGLWLAAVDAVWPDPQAREQAGRWLLAAEAAGAELSARALVQRASLLPDTVQHYAERIARLADPASPAAPREALGRDLAEVKQSNPALRALAAQVLPALAADRAACANDIERAQFERLRKLADDPWLSADLPEWSLPTPQGRRRLWETAGALSASAPDAPGLQSPHDVAALGDGRYLVALGEAGAAVVDRNGRRVRSYAVPAYRFVMSHSGQIALAIARRDSVSRIARLDLAHHEITDLGAMPLQFFADRFDGIAWSVVSGERIMVVDAARASLDVLWSVGDLGGPVVAAEFFPIEESFLVHGDREQVLWRYRNAPQRRLLSRDPILEDGRFRQLHPAMGALPLQLTQDDDGAVRFAYTWGTRDFQMRLSPPPGELSGHGVIPLTQGCLVWLRGERAMRLHLVRLSHADVAASIDWPSAALRTREYEGGVLLFDHQGRVMDIASETSKVRVFALL
>NZ_CP011130.1|WP_057921189.1|1944412_1946272_+|hypothetical-protein
MRLPDTLKPWHAWLGWFDPELAGVLGELMLRLHPMLGAFRMRALRGAVEPEGIDDLRRRGSYERLLLSEWAMAEVVPEEFDRRAAAGEHLFLSPKLVAREVDALTVAVFDTGPTQLGAPRLVHVAMWILLAQRAQAAKARFAWGVLGKPGELHAADTPQALKRLLDARTYTPGGAVVARDGLDPEHAALSLSERLEREWTLRLDAADPIPGERWSIGSHAHGYGLGHRVDVQRASQDGLAIVIAARQARRELRLNLPDPNVSSRLLRGRFESVAREQSVLPGTGRLSLKQPPLISFGGNSVAVPLIGENAANVYRLPRGTMRSQSPPKTTRWSKEKTLLAATLVGRHFGGVIAHSDRLEFWQLAPLRRADLPPVEEFDPAASRARLLPCFVLNGTFNASPYARVLLLSGQGRLLSWTHNKFTARGAEYQIFAGRTLAIANAGNDHALHLRQLGNELHYEFLGVQTGRILEKIALQGEARAGFVCGRWFGSGWHGGCCVEQPVGGHGGERSSIWRVFLRSQHRAKSADHEIVLPADWKVVGLRMNAADELDLIALRPDRRAVVSIGAQGRATLYESPYQISVASVATDCDMIALVDLRGRLVVLRDNAKSVLLYAGGGDE
>NZ_CP011130.1|WP_057921188.1|1943992_1944409_+|hypothetical-protein
MKWGWRSEADPPPPQGAVGVGAAAHGLLDAIERLDESVRERLMLTANDDVVILTGATQSLPWSEGVAYVAPRADAPALWLSTVERPDLPLDLLHRAIARRHPQSPLLLLREPARIVPLHRALPATAALIAQIRSHWRG
>NZ_CP011130.1|WP_036114778.1|1942853_1943996_+|AAA-family-ATPase
MTLPIEPSAAQQAAARVRDAVHSATVGLIEREQLAELIVLAAVAQEHLLILGPPGTAKSAVVRRVASALGGRYFEYLLGRFTEPSELFGPVDLRRLREGVVETDVSGMLPEAEVAFLDEVFLGSTAILNTLLGVLNERRFRRGHTQIECPLRVCVGAANALPDDESLAAFADRFLLHLFVEPVPDHQLEALLEGGWQSERAPLAHRTELSDIDELSRRVPLVDLSHARGLLADAIRKLRAAGLSLSDRRIVKVQRLIAAATVLAGRDTATDADLWPLFYVMPTREAQASAQDVLRDSMSAAANPTLRAAVEHAVLQPVSRAARLVEAARSCLQGGADAPAAATIAEALLREIDANFDAKSLPPELAAERARLIERVATPT
>NZ_CP011130.1|WP_036114799.1|1941223_1942591_-|ATP-binding-protein
MPDTSLDDLLAALAASPQNPALRMLVVNACLAEADPDALTRALELAGDDLLNDPTQRDAAVRVLLQHGRDELVARIAPDDSAAALFALARLRLADGDRDSARGLYQQAVALNPALEDAALANELAGKVISFANAKRQQSEGLRPGAQASLANDDTDADDVARLLQPPQARIAFADVGGLDEVKHQIRRRIITPFLKPSLFERFKRRSGGGILLYGPPGCGKTLLARATAGECGAKFYNVAITDVLDMYIGESERKLHAIFETARRTAPAVVFFDEVEAIGGKRQYSREATSAKLVSQFLTELDGFAQNNHGVLILGATNVPWAVDAAFRRPGRFDRVLFVPPPDETARRAIVDLLLRDRPLGEGIDVGELARLTSGFSGADLRNLVETAIDEAIEDSIEQGRESPLTMTHLRAALKDTRSTTLEWLTTARNHARYANQGGQYDEVLDFLKRHGGG
>NZ_CP011130.1|WP_036114782.1|1940747_1941224_-|hypothetical-protein
MAALPYRLPDEPRPSGLSRYAVDPLWPLLTLMLAGGGFGLAWFAFNSAALGSPTRGREWACVALSVFGTVALVFTIGVLLGSGWLRPEHQAYAFLSLLLLKVGVAYALYLMQQRCFEIFEHYGGEPRNGMPLMILLAVVGRGALDMTGWPLMLRMVLQ
>NZ_CP011130.1|WP_057921187.1|1939824_1940751_-|tetratricopeptide-repeat-protein
MSRHDHFYRMAERYYANGQVDDAIGMLLQALGEDPDQSDAHAFLSLCLIKRNRLHAAELEAGRALELEPESPFAHLAAAIAAIARRSLKQAQAHLDSARELQPDSAAIADAYARLYLAWGRDAQALEEARRACELDPDDPDYPALLASLELRRGDRARAEALARDVLRGHPEHVEALCVLGHCELAAGRTDSARDHAAWALQIDPMDGEALTLMAAVKARRSWALGLWWRFQSFISAGSRTRAVVLLIGMFLIYRIALIALPQNGLPQWTGPLSYAWLLFCAYTWIAPSLFWRSVKKELEQVKLRPGF
>NZ_CP011130.1|WP_187313403.1|1954912_1956997_-|peptidase
MLLSLAIAAALAACSKPETPAPATGTPAAKPAEATALTLDESKLPQPVRFAVADLDPAKNACDNLGEYVNGRWFAANPIPGDRSSWGVSDVLAERSLAVQHQLAQQAAADPKASGVEKLIGDLWSTGMDEAKINAQGLTPVQADLAAIAALDSPEKIAAYLRSSAAQGHNVVFGFGAEADFKNSSMNIAFATQGGLGLPDKGYYFDKDKHDKLAAYQQHIAKVLELSGVAAADAAQQAKAVIDFETRLARASLSSEQLQRDVALYYQPISVAAANELTPNFSWTKFFESQGVATPAQFSLAMPDFHKEVSKMIADTPAATWQAYLRYHTVDDASPYLADNFVAEHYEFHNKTMRGQKEPKARWKRVLGDIDDQAGEAMGQLYVKVAFPQQSKAQMETLVQGLRTALKARIENLSWMSDETKKKALEKWASFTPKIGYPDKWRDWSGLKTDRDSYYANAQAAYRFNYQWNLSKIGKPVDKTEWGMSPQTVNAYYNPLQNEIVFPAAILQPPFFDPKADEATNYGGIGAVIGHEMTHGYDDQGSRFGPDGNFNNWWTPADAKGFAERSAKLVQQFDGYQAAPGLKVNGKLTLGENIADLGGIATAYDAMRLAVGDTPDPKTDGLSRDQRFFYSFATSWRDRYTPDMLKVLVNSDPHAPSDFRAIGAPSNLPAFAAAFSCKPGQPMVRGAAEQVVIW
>NZ_CP011130.1|WP_057921192.1|1957436_1958810_+|MBL-fold-metallo-hydrolase
MRVHFHGAAGEVTGSLHEVEAAGHRILLDCGMIQGSPEAELRNLDAFAFDAATLDALVISHAHIDHIGRVPLLVKRGFRGPIFAQAATADLMRIMLLDSASIAESEAERGNRRRAHGEPELLPLYTREDVEATMQRVQPLPYDTRREILSGVTVQFREAGHILGSSVVELFADGRKLVFSGDLGPKGTPILRDPAPIDSADLVLMESTYGDRLHKDRAETILELGRILDAAWNDGGNVLIPAFAVGRSQELLYWFAKYWDEWNVGRFKIFLDSPMASKVVGVYDRHVELFDEDALRVWKHKPDPFHLPNLQLTESAQDSMAINQIERGAIVIAGSGMANAGRILHHFKHNLGKPQTHVVFVGYQAEGTIGRRLVEGAKWVRIHGRDTRAEAQRHTIGGLSAHTDQNGLIEWYGRIEGHPPLVLVHGEDKAREALAGEIGERFGTKVALARPGMMLDL
>NZ_CP011130.1|WP_057921193.1|1958976_1959393_+|hypothetical-protein
MSILILQGRHLSSKPLQSHFLLELRGLAAAVGRNLELRPCASLRELVGSLRAARRRRSEFVLLDPGELAPQALAEPEALRQALDELPSAYIEVHDASATTLDDRLRAHAPPLATIVINGDLAMSYRIALGIALRRLSR
>NZ_CP011130.1|WP_057923484.1|1959456_1961001_-|BCCT-family-transporter
MVFRLSIVLLAALVAAGVLAPQSFNETIQHALSLTVARAGWLYLLIVFASLLFLLYLSLGRFADLRIGGDDAEPEFSRLSWLSMLFAAGMGIGLVFWGAAEPVSHYLHPPEGLAAQSMPAARASMRYVFFHWGLHPWAVYALVGLAMAWFQFNRNGRGQISDLLQPVIGRWHRRWPGQLIDVAAVVATAIGVATTLGFGTVQISAGLARVFGLSVTPALQLCVVAVAFALYMASSLTGLHRGIKWLSNLNLALAALLLAFVLVAGPTSFIFETFTTTLGSYINQLPNMSLRMAPFSRDPWVGEWTIFYWAWWIAWAPFVGSFIARISRGRRVREFVFGVVLVPSMMSFVWFAAFGGSALWAQMFGGVDLAGALGQGYEQVLFALLESLPWAPLLIAAAIALLMLFFVTSADSATLVLASMSSEDRADPPLSRRATWGVIQALIAVALLLAGGLDALQGVIIVAALPFALLLVLIMWSLYRVLDQEYLHKQREATRFRHAMQRWLARENDGAAPV
>NZ_CP011130.1|WP_057921194.1|1961364_1961880_-|DUF3304-domain-containing-protein
MSLWKNPLMILLCAGTMALAACEDPMTIASITGYNHHTEASGLYVQGFSVDDASGSNAEPEGGAGATCCVQIPKRWHPGLQAKVKWSYSRLANDKRPIPPPREAAVDIPDYNARGPGSLQVHFYPGEKLKIVISSLGIEHPYYPMSETDKRPWQTSKERLEYLRANPEQKD
>NZ_CP011130.1|WP_057921195.1|1961961_1963161_-|low-temperature-requirement-protein-A
MTDPRPTLLRSREGHAKVGYAELFFDLVFVFAVTQLSHTLLEHLDPVGALRTGLLFLGVWWLWIYTSWVTNWLDPEKVPVRLMIFGLMLGGLLLSSSLPDAFGERGLIYAAVFASMQVGRSAFMLWALRGGRSPGNFRNFIRITLWLLVSGGFWIAGGLAEPDARVGWWMIAIGIEYLGPIAFFRVPGLGRSTLSDWDVEGGHLSERCGLFIIIALGESILITGATFAKLDWNPTTVAAFCIAFLGSVAMWWIYFDSGAARGEHRIAHDEDATRRARLARLAYTYMHLLIVGGIIVCAVADELVLVHPDHADAAGIAAIVGGPALYLLGCALFKWVTNTRRFPPISHCAGLLMLAALWFASAPLHLSALMLGAATTLVFMIVAGWETAALRRMPASATH
>NZ_CP011130.1|WP_057921196.1|1963175_1963460_-|hypothetical-protein
MHTVLVILGGFALLALCLLAARVLVGPGTAPLRSAIRIFLPLWLIGAGINMAVGVIHAGYSVAEELPIFALIFAVPAAFALVLGWILSRTRSTP
>NZ_CP011130.1|WP_057921197.1|1963633_1964407_-|SDR-family-oxidoreductase
MPNRSLTGKAVVIGGGAKNLGGLISRELAAGGAGAIAVHYNSDATRAAAEETVAAVRAAGADAFAHQGDLTRPGEVAALFDAAKARFGKLDIAINTTGMVIKKPLIEVTEAEYDRMFAVNAKAAFFFIQQAGKQLADDGNICTIVSSLLAAYTPFYAVYPGSKAPIEHFTRAASKEFGERGISVNAVGPGPMDTPFFYPAESKESAAYHATAAALSSRTRSGLTEIADIAPLIKFLVSDGWWITGQTIFANGGYTTR
>NZ_CP011130.1|WP_187313365.1|1964567_1965437_+|helix-turn-helix-transcriptional-regulator
MSHPDPGQRELMRRELSLGDGVLFAFAAERIAEPTQWSVHHDRHTLIVHLDGTMRRLETRIEGVGRLRAPAAAGDLWLIPAGRRYQGEARGGEIAYAELTIDPARYPGLRDTPAGGTDLAARMKHHDPLVHALAARLAQLSGEPDDLAAMLCDTLSQSLCLHLLREHGAAAAPSRPPREPSPRLSEPQRRRVEDYIASHLDQPIRLAALAALTGLSTHRLLIAFRASFGATPIQYVLAQRLQRVCMRLRRGDDDITTIAIGSGFSSHSHLSAVFKRQYGITPSEYRQRG
>NZ_CP011130.1|WP_036114746.1|1965769_1966666_+|ABC-transporter-ATP-binding-protein
MLTIRDLTKTYANGVRALDGISLDIPRGMFGLLGPNGAGKSSLMRTLATLQEADAGSAILDNGDGPAIDVLRDKDAVRRQLGYLPQDFGVYPKVSALDLLEHFAVLKGLTNRKQRREVVDGLLHQVNLWNVRKQKLGGFSGGMRQRFGIAQALLGDPRLVIVDEPTAGLDPEERNRFLNLLAEIGENVAVILSTHIVEDVTDLCPSMAIVNKGKVLLSGEPNAAIAALSDQVWRKQVSKATLSSYETRFTVLSTRLVGGQPVIHVFSPDSPEEGFERVAPDLEDVYFQRLRQHARVAA

Crispr_ID: NZ_CP011130_9

• CRISPR_ID: NZ_CP011130_9
• CRISPR_location: 3315990-3316090
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_9

Consensus_repeat	Method
GCAGAGCCCGCCTTCGCGGGAAT	CRISPRCasFinder

spacers of NZ_CP011130_9

>9.1|3316013|55|NZ_CP011130|CRISPRCasFinder
GACGACCTCAGACAATGGCCTGAAGTCTCCCAACGCGCGGCTTCGCCGATGTAAG

CRISPR arrays and Neighbor proteins around NZ_CP011130_9

CRISPR arrays

The CRISPR arrays of NZ_CP011130_9

>merge|NZ_CP011130|9|3315990-3316090|CRISPRCasFinder
GCAGAGCCCGCCTTCGCGGGAATGACGACCTCAGACAATGGCCTGAAGTCTCCCAACGCGCGGCTTCGCCGATGTAAGGCAGAACCCGCCTTCGCGGGAAT

>NZ_CP011130|9|8|3315990-3316090|CRISPRCasFinder
GCAGAGCCCGCCTTCGCGGGAAT	GACGACCTCAGACAATGGCCTGAAGTCTCCCAACGCGCGGCTTCGCCGATGTAAG
GCAGAACCCGCCTTCGCGGGAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057921770.1|3304218_3306174_-|5-dehydro-2-deoxygluconokinase	unknown	unknown	gnl|CDD|378281
NZ_CP011130.1|WP_057921773.1|3310427_3311420_+|inositol-2-dehydrogenase	unknown	unknown	gnl|CDD|275173
NZ_CP011130.1|WP_187313213.1|3328406_3329942_+|ankyrin-repeat-domain-containing-protein	unknown	unknown	gnl|CDD|320700
NZ_CP011130.1|WP_057921780.1|3324172_3327676_-|chromosome-segregation-protein-SMC	unknown	unknown	gnl|CDD|274008
NZ_CP011130.1|WP_057921779.1|3320191_3322555_-|NAD-dependent-DNA-ligase-LigA	unknown	unknown	gnl|CDD|236137
NZ_CP011130.1|WP_057921775.1|3312635_3315386_-|DNA-gyrase-subunit-A	unknown	unknown	gnl|CDD|235502
NZ_CP011130.1|WP_057921778.1|3319196_3320195_-|EF-P-lysine-aminoacylase-GenX	unknown	unknown	gnl|CDD|273090
NZ_CP011130.1|WP_057921777.1|3318363_3319092_-|DUF3011-domain-containing-protein	unknown	unknown	gnl|CDD|371422
NZ_CP011130.1|WP_057921768.1|3301368_3302286_-|myo-inosose-2-dehydratase	unknown	unknown	gnl|CDD|275172
NZ_CP011130.1|WP_057921769.1|3302278_3304222_-|3D-(3,5/4)-trihydroxycyclohexane-1,2-dione-acylhydrolase-(decyclizing)	unknown	unknown	gnl|CDD|275170
NZ_CP011130.1|WP_046656746.1|3317406_3318174_-|DUF3011-domain-containing-protein	unknown	unknown	gnl|CDD|371422
NZ_CP011130.1|WP_057923563.1|3330064_3331627_+|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_CP011130.1|WP_036104280.1|3306214_3307006_-|sugar-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224053
NZ_CP011130.1|WP_036104303.1|3323146_3323917_-|cell-division-protein-ZipA	unknown	unknown	gnl|CDD|235308
NZ_CP011130.1|WP_148650387.1|3307016_3308138_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224093
NZ_CP011130.1|WP_036104288.1|3309568_3310435_+|MurR/RpiR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224651
NZ_CP011130.1|WP_036104308.1|3328002_3328395_+|BlaI/MecI/CopY-family-transcriptional-regulator	unknown	unknown	gnl|CDD|367747
NZ_CP011130.1|WP_057921772.1|3308283_3309372_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|380535
NZ_CP011130.1|WP_057921776.1|3316200_3317259_-|S-methyl-5-thioribose-1-phosphate-isomerase	unknown	unknown	gnl|CDD|235578
NZ_CP011130.1|WP_057921774.1|3311486_3312509_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|275173

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057921770.1|3304218_3306174_-|5-dehydro-2-deoxygluconokinase	gnl|CDD|378281	pfam09863, DUF2090, Uncharacterized protein conserved in bacteria (DUF2090). This domain, found in various prokaryotic carbohydrate kinases, has no known function.	6.63402e-160
NZ_CP011130.1|WP_057921773.1|3310427_3311420_+|inositol-2-dehydrogenase	gnl|CDD|275173	TIGR04380, hypothetical_protein_HOLDEFILI_04020, inositol 2-dehydrogenase. All members of the seed alignment for this model are known or predicted inositol 2-dehydrogenase sequences co-clustered with other enzymes for catabolism of myo-inositol or closely related compounds. Inositol 2-dehydrogenase catalyzes the first step in inositol catabolism. Members of this family may vary somewhat in their ranges of acceptable substrates and some may act on analogs to myo-inositol rather than myo-inositol per se. [Energy metabolism, Sugars].	5.69257e-148
NZ_CP011130.1|WP_187313213.1|3328406_3329942_+|ankyrin-repeat-domain-containing-protein	gnl|CDD|320700	cd07341, M56_BlaR1_MecR1_like, Peptidase M56-like including those in BlaR1 and MecR1, integral membrane metallopeptidase. This family contains peptidase M56, which includes zinc metalloprotease domain in MecR1 as well as BlaR1. MecR1 is a transmembrane beta-lactam sensor/signal transducer protein that regulates the expression of an altered penicillin-binding protein PBP2a, which resists inactivation by beta-lactam antibiotics, in methicillin-resistant Staphylococcus aureus (MRSA). BlaR1 regulates the inducible expression of a class A beta-lactamase that hydrolytically destroys certain ?-lactam antibiotics in MRSA. Both, MecR1 and BlaR1, are transmembrane proteins that consist of four transmembrane helices, a cytoplasmic zinc protease domain, and the soluble C-terminal extracellular sensor domain, and are highly similar in sequence and function. The signal for protein expression is transmitted by site-specific proteolytic cleavage of both the transducer, which auto-activates, and the repressor, which is inactivated, unblocking gene transcription. All members contain the zinc metalloprotease motif (HEXXH). Homologs of this peptidase domain are also found in a number of other bacterial genome sequences, most of which are as yet uncharacterized.	4.48157e-42
NZ_CP011130.1|WP_057921780.1|3324172_3327676_-|chromosome-segregation-protein-SMC	gnl|CDD|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0
NZ_CP011130.1|WP_057921779.1|3320191_3322555_-|NAD-dependent-DNA-ligase-LigA	gnl|CDD|236137	PRK07956, ligA, NAD-dependent DNA ligase LigA; Validated.	0
NZ_CP011130.1|WP_057921775.1|3312635_3315386_-|DNA-gyrase-subunit-A	gnl|CDD|235502	PRK05560, PRK05560, DNA gyrase subunit A; Validated.	0
NZ_CP011130.1|WP_057921778.1|3319196_3320195_-|EF-P-lysine-aminoacylase-GenX	gnl|CDD|273090	TIGR00462, genX, EF-P lysine aminoacylase GenX. Many Gram-negative bacteria have a protein closely homologous to the C-terminal region of lysyl-tRNA synthetase (LysS). Multiple sequence alignment of these proteins with the homologous regions of collected LysS proteins shows that these proteins form a distinct set rather than just similar truncations of LysS. The protein is termed GenX after its designation in E. coli. Interestingly, genX often is located near a homolog of lysine-2,3-aminomutase. Its function is unknown. [Unknown function, General].	7.92181e-127
NZ_CP011130.1|WP_057921777.1|3318363_3319092_-|DUF3011-domain-containing-protein	gnl|CDD|371422	pfam11218, DUF3011, Protein of unknown function (DUF3011). This bacterial family of proteins has no known function. Most members belong to Proteobacteria.	2.30466e-56
NZ_CP011130.1|WP_057921768.1|3301368_3302286_-|myo-inosose-2-dehydratase	gnl|CDD|275172	TIGR04379, myo-inositol_catabolism_protein, myo-inosose-2 dehydratase. Members of this family include the enzyme myo-inosose-2 dehydratase, product of the gene iolE, as found in inositol utilization cassettes in many species. [Energy metabolism, Sugars].	5.91233e-157
NZ_CP011130.1|WP_057921769.1|3302278_3304222_-|3D-(3,5/4)-trihydroxycyclohexane-1,2-dione-acylhydrolase-(decyclizing)	gnl|CDD|275170	TIGR04377, 3D-35/4-trihydroxycyclohexane-12-dione_hydrolase, 3,5/4-trihydroxycyclohexa-1,2-dione hydrolase. Members of this protein family, 3,5/4-trihydroxycyclohexa-1,2-dione hydrolase (iolD), represent one of eight enzymes in a pathway converting myo-inositol to acetyl-CoA. IolD hydrolyzes the cyclic molecule 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione to yield 5-deoxy-D-glucuronic acid. TPP is a cofactor. [Energy metabolism, Sugars].	0
NZ_CP011130.1|WP_046656746.1|3317406_3318174_-|DUF3011-domain-containing-protein	gnl|CDD|371422	pfam11218, DUF3011, Protein of unknown function (DUF3011). This bacterial family of proteins has no known function. Most members belong to Proteobacteria.	2.09985e-58
NZ_CP011130.1|WP_057923563.1|3330064_3331627_+|serine-hydrolase	gnl|CDD|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	1.03605e-47
NZ_CP011130.1|WP_036104280.1|3306214_3307006_-|sugar-ABC-transporter-ATP-binding-protein	gnl|CDD|224053	COG1129, MglA, ABC-type sugar transport system, ATPase component [Carbohydrate transport and metabolism].	4.32698e-103
NZ_CP011130.1|WP_036104303.1|3323146_3323917_-|cell-division-protein-ZipA	gnl|CDD|235308	PRK04570, PRK04570, cell division protein ZipA; Provisional.	2.70229e-117
NZ_CP011130.1|WP_148650387.1|3307016_3308138_-|ABC-transporter-permease	gnl|CDD|224093	COG1172, AraH, Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components [Carbohydrate transport and metabolism].	8.88452e-71
NZ_CP011130.1|WP_036104288.1|3309568_3310435_+|MurR/RpiR-family-transcriptional-regulator	gnl|CDD|224651	COG1737, RpiR, Transcriptional regulators [Transcription].	1.37454e-56
NZ_CP011130.1|WP_036104308.1|3328002_3328395_+|BlaI/MecI/CopY-family-transcriptional-regulator	gnl|CDD|367747	pfam03965, Penicillinase_R, Penicillinase repressor. The penicillinase repressor negatively regulates expression of the penicillinase gene. The N-terminal region of this protein is involved in operator recognition, while the C-terminal is responsible for dimerization of the protein.	3.54336e-34
NZ_CP011130.1|WP_057921772.1|3308283_3309372_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|380535	cd06312, PBP1_ABC_sugar_binding-like, periplasmic sugar-binding domain of uncharacterized ABC-type transport systems. 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.	9.88426e-103
NZ_CP011130.1|WP_057921776.1|3316200_3317259_-|S-methyl-5-thioribose-1-phosphate-isomerase	gnl|CDD|235578	PRK05720, mtnA, methylthioribose-1-phosphate isomerase; Reviewed.	3.01239e-179
NZ_CP011130.1|WP_057921774.1|3311486_3312509_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|275173	TIGR04380, hypothetical_protein_HOLDEFILI_04020, inositol 2-dehydrogenase. All members of the seed alignment for this model are known or predicted inositol 2-dehydrogenase sequences co-clustered with other enzymes for catabolism of myo-inositol or closely related compounds. Inositol 2-dehydrogenase catalyzes the first step in inositol catabolism. Members of this family may vary somewhat in their ranges of acceptable substrates and some may act on analogs to myo-inositol rather than myo-inositol per se. [Energy metabolism, Sugars].	1.03663e-108

Protein sequences

>NZ_CP011130.1|WP_057921775.1|3312635_3315386_-|DNA-gyrase-subunit-A
MAELAKEIIQVNLEDEMRRSYLDYAMSVIVGRALPDVRDGLKPVHRRVLYAMSELGAHSNKPHFKSARIVGDVIGKYHPHGDQSVYDTLVRMAQPFSLRYLLVDGQGNFGSVDGDSAAAMRYTESRMAKLTHELMADIDKETVDFQPNYDEKELEPTVMPTRVPNLLINGSAGIAVGMATNIPPHNLSEVINATIALINAPELDVDALMEYIPGPDFPTAGIINGTAGIINAYRTGRGRVRMRARAEIEVNQDTGREAIAVTEIPYQVNKARLIEKIAELVKEKRLEGISELRDESDKDGMRIFIEVKRGESAEVVLNNLYQQTQMESVFGINMVALVDGRPQLLNLKQILEAFIRHRREVVTRRTIFELRKARQRAHILEGLTVALANIDEMIELIKTSANPNEARERMLEKTWEPGLVGALLAAAGSEASRPEDLAAEFGLHDGRYQLTETQATQILEMRLHRLTGLEQEKLTDEYKVLLEAIRGLIEILENPDVLLEVIRTELLNLKEEFGDARRSEIRASEEDLDILDLIAPEDVVVTLSHSGYAKRQPVSAYRAQKRGGKGRNAAMTKDEDFIDKLWLVNTHDTLLTFTSTGRVFWLPVHQLPDAGPNARGRPIINWLALEAGEQVQAVLPVRAYDDSHFVFFATRNGMVKKTPLTEFAYRLARGKIAINLDDGDALVDVALTNGQREVMLFASNGKAVRFAESGREDDADAVEESVDTDGAEDSGEDAVEVVAEGEGADRSRRGKGGVRSTGRNSRGVRGIKLAKGESVVSMIVIDGDGDILTASQRGYGKRTPVDEYPCKGRGTQGVIALKTTERNGALVGAIQLSDHHEVLMISDGGTLVRTRAAEISQVGRNTQGVTLMRLAEDETLQTIERVDASLDEVEDGIEGEVPAAPVADAGDAVETPATDA
>NZ_CP011130.1|WP_057921774.1|3311486_3312509_+|Gfo/Idh/MocA-family-oxidoreductase
MSQKLLKIGVAGLGRLGRRYAENLARHVPRARLDAVCSPIADEVDWAREQLGVQRAYADYAAMLADPELDAVFLITPTSLHPQQIEQALDAGKHVFCEKPLSLRMDECQRTVEHARRHPGLRAMVGFVRHFDASYRQAKTRIDDGAIGKPFLVYSQTADLFDPSGAFVKFAPTSGGLFLDCSVHDVDLARWLLGRPKARRVYAMGTIAAYPDLQAIGDIDNGVAVCEFDNGCMAMFYASRTQAHGHETCTDVVGTAGKLSIGRNPRLDRLEIADAHGVRSLSTANFFERFGDAFLSQCSHFVDAVLDDQPFDLDLEDAAEATRIAIALRESLQTRQPMDL
>NZ_CP011130.1|WP_057921773.1|3310427_3311420_+|inositol-2-dehydrogenase
MIEVALFGAGRIGKIHAANLARHPKARLHYVVDVHDAAAAELARAHGARVASAEQALADPAVSAVVIGSSTDTHADLIQRSALAGKAIFCEKPVDLDIGRARACADTIARTGVACMIGFQRRFDPTFRALKQRLDAGEIGAPEVLLITSRDPGPPPLDYIARSGGVFKDMLIHDFDIFRWILGAEAVSVYATGAAPEFAEIAAAGDLTTAAVTLRTREGALCQINTSRRAAYGYDQRFEVLGSRGLLQAGNLRPTEVVAWNAQAISQDTPEAFFLERYRAAYALEIEHFFDGLSQGTPLHPNIDDGIKALELAELATRSWREGRALDCSI
>NZ_CP011130.1|WP_036104288.1|3309568_3310435_+|MurR/RpiR-family-transcriptional-regulator
MSTYQGVDELMQGIAAEFDNLPRQLQSVARYIEQQRANLMVQRINEIAEGSGVHSSAVVRFAQRFGFSGFTEMQALFRNAYTEQVAPARSYQQRIRRVIEDDGGRMTSAQMALRFIDASRLGLDELAAEFDAERFQSAVDLLVKAENIYVVAVRRSFSIASYIAYALQHTNKRVHLITGLGGMHREQIRSIGKNDVLIAISFPPYGKETLFCARVARERHAKVLAVTESELGPLANYADVLLKVQEGSAFAFRALTSTICLCQALFVALTYELELKVEETNRPGEYDD
>NZ_CP011130.1|WP_057921772.1|3308283_3309372_-|sugar-ABC-transporter-substrate-binding-protein
MRVIGSFLNGRFGLRSVSIALALVLSACSGGGEASSAPASAGGGRGGERYVLVSHAPDSDSWWNTIKNSVVDAGEDFGVAVDYRNPPNGDLADMARLIEQSAARNYAGVATSIADFSVLSKATSRVTGKGIALVTINSGTREQSKQLDAIMHIGQPEYDAGKAAGERAKAAGVTSFLCVNHYATNLASVERCKGFADALGADLRASMLDTGVDPTVVSSKVGAYLRNNPKTGAVLALGPNSAEPTLQVLKQMGLAGKIFFATFDLSPTIVQGIEDGELNFAIDQQPYLQGYLAIAALKIAHDEATRDPAVIVAKLRAHPKIQARLKQYALEPVYTADGVSSGPGFVTRERLDVIKKYAGQYR
>NZ_CP011130.1|WP_148650387.1|3307016_3308138_-|ABC-transporter-permease
MATSMNDLPGQRKDERVRPIAFWRAFAARPEFGSLAGAVLVFALFAVFAGDSGMFNLDGVMNWSQVAAYLGIIAVGACLLMIAGEFDLSIGSMIGFAGMLMAVPAMFLGWPMWAAVAFTFVCCAALGWLNGYLVVRTGLPSFIVTLAFMFILRGLTLVLSTHFSNSTVVSGVGDAVARDPLISALFRGAALPGLFEWLANSGAIDRLPNGKPVVEGIPKVLLWWGALAAAAGFVLSRTRTGNWIFTVGGDATAAKNVGVPVRRVKIGLFVVTALCACLFGVLQVADIGSAAADRGLQKEFEAIIAAVIGGALLTGGYGSIRGACIGALIFGVVQIGISYTDINSDWYRVFLGAMLLLAVLLNHYIRLRATGAK
>NZ_CP011130.1|WP_036104280.1|3306214_3307006_-|sugar-ABC-transporter-ATP-binding-protein
MNDDCILQLENVSKYFGSVISLKDVSLRLRRGEVHCLLGDNGAGKSTLIKTLAGVHRPSEGRYLVEGQPVCFKSPREALDRGIATVYQDLALVPLMSVARNFFAGREPRRKLMGLIPVMDLDFAAETAMTKLAEMGIHVRSPHQPVGTMSGGERQCLAIARAIHFGAKVLILDEPTAALGVKQSCNVLMLIHQARERGISVIFITHNVHHAYPIGDSFTVLNRGQSMGSFAKHEISKERVLDMMAGGSEIQTLFDRLEGRSAA
>NZ_CP011130.1|WP_057921770.1|3304218_3306174_-|5-dehydro-2-deoxygluconokinase
MNDRALDAIFLGRVAVDLYAQQTGARLEDVASFAKYLGGSSANAAFGLARLGLRSAMLSRVGDDHMGRFLRETLAREGCDVSRLRTDPDRLTALVLLGIKDRDTFPLIFHRENCADMALSAADIDEDFIASSRALAITGTHLSSAGVHAASLRALEFARRHGVRNVLDIDYRPVLWGLTGRGDGETRFIADDGVTRHLQSVLPLFDLVVGTEEEFLVAGGGSDLVAALRAVRAVTSALLVVKRGAQGCSVIEAAVPADIDDAPTYRGTRVEVLNVLGAGDAFMAGFLSGWLREEPIERCCAYANACGALVVSRHGCAPAMPSRAELDYFLANAERLRRPDRDEQLAHLHRVSVARAQWDDLHVFAFDHRSQLFELARECGAPESRLPRLKSLLVQAVDRAERSLDLHGRIGLLCDETYGQDALDAATGRRWWIGRPVEMPGSNPLEFEYGRSIGTQLSRWPLEHVVKCLVQFDPDGDAQARIEQETQLRGLYDAVRASGHELLLEVIPPADSEGRRGGERVLRSLKRIYNLGIRPQWWKLAPLPMRDWDALDALIEERDPYCRGVLLLGLNAPFAELAEGFASASRSRSCRGFAVGRSIFVEPARAWLRGDIDDETLVARACASFAELAALWARSRQVRCAPAAGTVGHAA
>NZ_CP011130.1|WP_057921769.1|3302278_3304222_-|3D-(3,5/4)-trihydroxycyclohexane-1,2-dione-acylhydrolase-(decyclizing)
MNATSSPASAAASGSGGVVRLTMAQALVRYLAAQYTIDPGSGERVRLFGGAFAIFGHGNVAGLGEALHQHRDALPTYRAHSEQGMANAAIAYAKAHMRRRMMAVTASIGPGSTNLVTSAALAHVNRLPVLLLPGDIFVSRAPDPVLQQLEDFADGTVSVNDCLRPVSRYFDRIVKPEQLLRALPRAMRVLTDPALCGPVTLALPQDVQTEAWDWPQAFFAPRLHVFRALSPQADEVATLAAALREAQRPVLIAGGGVLYGRAGDELRRFADLHRLPVAETQAGKGALAWDHPLQLGAAGVCGSSAANALLAQADLVLAVGTRLQDFTTGSNALYAGARIATINVNAYDALKGGGPELICDAGLGLRALSASLSDWHAPAPWAARARDEAQAWRAIVDAVTGRRELPAGTLPYDGEVIGAVQRSGARSDRDDIVVCAAGTLPAELEKLWRTRTPGGYHMEYGYSCMGYEIAGGLGVKMARPEREVVVMVGDGSYLMLNAEIASSVMLGMKLIVVVLDNRGFGCINRLQQACGGAAFNNMWDDCLHAGDGAPPIDFAAHARAMGAQAEHVADIDALEQAMRRARAARGTYLISIDTDHRRTTEHGGCWWEVAVPQVSERDAVRQARRDYEIAKQRQQPRPPAAQGDCDV
>NZ_CP011130.1|WP_057921768.1|3301368_3302286_-|myo-inosose-2-dehydratase
MSDGAFAVKIGINPIGWSNDDLPSLGGEIPLATALLEGRQIGYQGFELGNKFPREPEALRDLMAGYGLEVISGWYSGRLAQRGVEEEIAAVQAHLRLLAGNGCKVMVYGEVVDAIQGERDVALHKRPRFADEDAFARYGERVTAFARYLLEHGVRLAYHHHMGAYVESPGDIDRLMAATGEEVGLLFDSGHAYFGGGDPLALLRRHIGRVCHVHCKDVRPELIKLARNRHWSFLDSVLNGVFTVPGDGAIDFAALIGVLREHGYAGWLVVEAEQDPAVAPSYAYAERGYLTLRALVDGASLEEVA
>NZ_CP011130.1|WP_057921776.1|3316200_3317259_-|S-methyl-5-thioribose-1-phosphate-isomerase
MNDTIDFDRYDRIRPIRWTGQALELLDQRKLPFAVEYVSCEDSDAVAAAIHALTVRGAPAIGIAAAWGVVLAANTIEADDGATALARIEPAMQRLNAARPTAVNLAWALARMRRVLAVAGADWRDVLAREAQAIADEDLAANRRMGALGAALIAPGNGVLTHCNTGSLATAGFGTALGVIRAGVAQGRIAQVYAGETRPWLQGARLTVWELEQDGIAPILIADSAASHLMKTGKVGWVIVGADRICANGDTANKIGTYQLAIAARHHGVKFMVAAPSSTVDMETASGDLIEIEERDPGELFAVGGTRTAAERVGAWNPVFDVTPHELIDAIVTERGVIERPDAAAMKAAFGG
>NZ_CP011130.1|WP_046656746.1|3317406_3318174_-|DUF3011-domain-containing-protein
MSARILSSLGLMVGLGLSAGVAQAAPQYNDYGYGSDNGVIRCESDGGRQRRCDADTRGGVQLSRQLSSSSCIQGRSWGYDRNGIWVSEGCRAEFALGRGGGWNGGGGGWNGGGNGDVVRCESDGGRQRSCSISGNRARLQRQLSSTTCIEGQNWGSRPGQVWVSGGCRGEFVATRGGGWNGGGGGNNGGGWGGGGQEISCESNNNRQNRCNMSVRRDVRLLRQNSGSPCIEGQTWGWDRNGVWVSNGCRGRFQVN
>NZ_CP011130.1|WP_057921777.1|3318363_3319092_-|DUF3011-domain-containing-protein
MRSVKAAIHLFAFAAAVCATSARAEPAGERMFGGDVLRCASQDEQTVRCPADTRGGVRLVRRTSGKPCVEGTSWGADRGGVWVSQGCSADFVLGRGGSGSDSRTGARVIKCESIGGRWNHCAANTEAGVVLAQQLSKQPCLRNQSWGTDGNGVWVSGGCRGEFRLLGAEPAAQAPGKLLLCESRDRKARRCDGETGQGVRMVKQLSNTECVEGRSWGYDAHGVWVEDGCRAEFELDYRRGGG
>NZ_CP011130.1|WP_057921778.1|3319196_3320195_-|EF-P-lysine-aminoacylase-GenX
MNPSAPRPPDWHPSASFETLRLRARLNATVRAYFAERAVIEVETPLMSVAGNTDPNIASFSLQFSGRTDGAPRTRWLRTSPEFPLKRLLAAGFGDCYELGRVFRDGEAGGRHNPEFTMLEWYRVGWDHRGLIEETADLVRAALALVGRDARLRTVAYRDLYRDRLGLDPMLADEAQLRAALGEVVIDPQGLNRDDWLDLLMTHRLQPQFSRDELLAIHAYPASQCALARVGEDRDGVAVAQRFELYLGPLELANGYHELADAAEQGARFDRDRERRGERGAVCPPRDEALLDALAAGFPDCAGVALGMDRLLMAMLDSARIADVLAFDFTRA
>NZ_CP011130.1|WP_057921779.1|3320191_3322555_-|NAD-dependent-DNA-ligase-LigA
MTTQSKQDAAQAAQRAAQLRAQLDDANYRYYVLDDPTLTDADYDRLLRELEALEVAHPELASADSPTQRVGNTPSGTFAQVTHVVPMLSLGNAFSDEEVTDFVRKIVERLDTANPEFSVEPKLDGLAISLRYENGRFVQGATRGDGATGEDVTLNLRTVKAIPMTLRGKDWPPVLEVRGEVYMPLAAFKTYNEKALKDGGKVLANPRNGAAGSLRQLDPRITAQRPLAFFAYAVGVVEGYTLPASHSQTLKKLRDWGFPVSAESGVVAGADGLLGYYRQMGAKRDSLPFDIDGVVYKLDDYAGQREMGFVSRAPRWAIAHKFPAQEQSTVLEGIDIQIGRTGAATPVARLKPVQVAGVVVTNATLHNADQIARLDVRIGDTVIVRRAGDVIPEIVRVVPEYRNPDAPQWQMPTACPVCGSEIVREEGEAAWRCSGELSCPAQRKEAIRHFASRRAMDIEGLGDRYIEDLSDLGYLQSVADLFKLKLEDLLEMKRRADERDGTTPETVKAGKVATKWADNLIEAIDQSRKTTLERFLFALGIQHVGENTSKALSGWLGDLQLIRRLPWPVFKRLPDVGGEVARSLGHFFDQPGNQQVIDDLLERGVQIADTHLPSPKLREGLNLATLLVDMEIPKVTKIRAEQLATAFADAGKLRDAPEHAYITAGLPADSAQALASWLSVDENAQLLTRVGDALKQLDALTPAASATSVGVLDGKTAVLTGSLAALTRDEAKARLEALGAKVAGSVSKKTSFVVAGTEAGSKLDKAQELGIEVWDEDQLLAFLAQNE
>NZ_CP011130.1|WP_036104303.1|3323146_3323917_-|cell-division-protein-ZipA
MSDVTLMRIGILIAGLILIGAIVFFGRPRKPGQGKRVAREDAARGAEPRKSGPRQEPTLGEQIQSELEQAGAPGEATTQAELELFDKTLEGNANAANSELGRRVSEEFDKIVTLYLAARAGHKLHGPDIVVAAEKAGLVYGHMGVYHRLVEGHPERGPVFSVANIMKPGSFDMAAIQSLETPAIAFFLTLPAPVAALDAWETMLPTAQRMAELLDAVVLDEQRNALGRQRIAHLRDELRAYDRQREAPPLSKPTRW
>NZ_CP011130.1|WP_057921780.1|3324172_3327676_-|chromosome-segregation-protein-SMC
MRLSTIKLSGFKSFVDPTTLHLPTNMTGVVGPNGCGKSNIIDAVRWVMGESSASRLRGDSLTDVIFAGSSARKPVSQAMVELIFDNSDHTITGEFAAFNEISVKRTVSRDGTSQYYLNGGKCRRRDITDLFLGTGLGPRSYSIIEQGMISQIIEAKPEDLRVYLEEAAGISKYKERRKETETRIRHTRENLDRLNDLREEVGKQLEHLRRQARQAEQYQAIQAERKIKDVEWKALEYRALDQKLQAQREKLSQQETRLQQLIAEQREAERELETGRVSREEAAAKLNKAQAASYEVGGALARIEQQIQHQREMSSRLLKARDEAMNQLAEIGEHIGSDQARLDVLLAAVADAEPRIEAMREDDEARQDALRDAENRLSDWQQRWDAHSREQSEAARAAEVERTRIEGLDRQTLDADRRREALASERAGLDLGALSEAFEQLQSQHDLQKESLESLTDELEIRKTAVSDLQEQQRATQNQLAEVRKQAQTSRGRLSSLETLQHAALGQEQGAALTWLKARGLDSAQRVGETLSVESGWENAVESALGQLIEGVLVESPETLVDAIGELGEGRLTLVSPERDDATYAATSLASKVQGPAAIRRLLTRLHGADDLAAARALQPSLGAEETIITRNGERLGAGWVRVLRSGAAKQGALLREREIQTLRVEIEELLTRERELEQTQIQLRDRSLAAEQQREDAQRALYMAHRSVSELAGQLQSHQGRLDSARNRIEKIDADLEQLLIGLDAGREQAREARMRQEAAVERMGELEDSRLQLESERRSLSEARDAARNAARESRDAAHALTLTLETQRAQIAGLSQTLERMGGQRGQLDSRLSELSAQLSDGDEPVVALEEQRQVALEQRVLAEQDLTAARSALDGIDNDLRKFEQTRQQRDEQALQQREAIGQRRLEQQALVLKAETLTEAIAEAGAVLQDVVNSLDENAEPQTWERSVIELDNKLRRLEPVNLAAIAEHAEAAQRKDYLDAQFLDLNTALETLEEAIRKIDRETRGRFKDTFDRVNSGVQELYPRLFGGGHAYLELTGEDLLDTGVAIMARPPGKRVSNISLLSGGEKAMTAVALVFAIFRLNPAPFCLLDEVDAPLDEANVGRFTAMVSEMSEQVQFLFVSHNKATMEAAQQLSGVTMREPGVSRLVSVDLAEATRLAGAA
>NZ_CP011130.1|WP_036104308.1|3328002_3328395_+|BlaI/MecI/CopY-family-transcriptional-regulator
MARPASPTLTQSEQAILEVLWDKDEASVREVADELSRHKSVAYTTVLTMFNVLAKKGFVTHRQEGRAFIYRAAISREQARKQALDHLLLQFFDGSPNLLAQHLLDRHDVDRAELKTLRDKVSAAKARGDA
>NZ_CP011130.1|WP_187313213.1|3328406_3329942_+|ankyrin-repeat-domain-containing-protein
MIESLIDAAPAFAAQHLLQSAVLFALAVVFMRMRALDAELRSWLLLAVFALALLAPLATLLPGPPSPAFTAPAEQLVPLPDEGPTPDEAIYEAGQRADVLYLEIPQSFSTVLALAWALGALWQLMRLVEGARQARRLRRCAHPAPALETLLAQELPRPARIATTAIDGPMVVGLLRPTILIPRALANTLDTSALRDILRHEIAHIRRGDLWLTAAVRVGLAAFWWNPLLRLIHARLDLAREMACDARAARACEARVDYAGSLLSSAETLLDLGERPIWLAVGMLERRSHLAQRIDGLIEPGPGDEPRRRHAAVAVCVAALLAFAGLALANTPRLDVSGRHVAEPDARVVALLAAAKAGDAATLRTLAANGVDIDARVLGDGTALIQAVTARNLSTVDTLLALGADPNRAALGEGNPLIVASRLGAQPIVERLVRAGADVNRVVTYDETPLINAARAGHLATVQYLIARGADVNLGMVADGWLGRWRSPLNQARDPAVRAYLIGRGAVAGHP
>NZ_CP011130.1|WP_057923563.1|3330064_3331627_+|serine-hydrolase
MKSMMLACTLAIGLLGAAAHAQTPAEPDVARLKAAIERGLRPSIVKAGETMPTWTLQERMAHHKIPGVAIAIVKDGKLLYAAGYGVREAGTHDAVDADTLFSVGSVSKMIAAATTLQLVAHGRIDLDRDVNAYLKSWRIPAAPAIKNPTVTMRMLLSHTSGLGVHGFQDYLPHETLPTLVQTLNGTPPAKNDPVRLQYEPGTRSDYSGGGIMLEQQIIEDLTGQPLDAVARAQVFEPAGMRRSTYENPLSPTRGNIAKAHDGNGALTALPRGWQTFPEQAASGLWTSANDLGAFVGALIQSYRGQGGLLPRAIALQMMSEVSPGVRGLGPELGGSGKARRFFHNGDNDSYHAAIEGYPETGYGFAILTNGENGGRIRGEIRNAISDALDDGMKPPIRTIALDLSAPAYADYAGSYRLDPAVPMDIRSALADWFDVESIAVKVADGAITMDVPDGPSASPLLPLSPTRFFASAAGAELEFHRNARGVVHAVSVVAGNSRAYYRRQVAQPAGAGAEPDRPRP

Crispr_ID: NZ_CP011130_10

• CRISPR_ID: NZ_CP011130_10
• CRISPR_location: 3461786-3461917
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP011130_10

Consensus_repeat	Method
CGACCGGATCGACCAGCGGCGCGG	CRISPRCasFinder

spacers of NZ_CP011130_10

>10.1|3461810|33|NZ_CP011130|CRISPRCasFinder
GGCTGTCGGCCGCGGGTTCGCCGAGCAATTGCG
>10.2|3461867|27|NZ_CP011130|CRISPRCasFinder
CCGGCTCGCTGCGGCGACGCAGCGAAT

CRISPR arrays and Neighbor proteins around NZ_CP011130_10

CRISPR arrays

The CRISPR arrays of NZ_CP011130_10

>merge|NZ_CP011130|10|3461786-3461917|CRISPRCasFinder
GGACCGGTTCGGCCGGCTGGGCCGGGCTGTCGGCCGCGGGTTCGCCGAGCAATTGCGCGACCGGATCGACCAGCGGCGCGGCCGGCTCGCTGCGGCGACGCAGCGAATCGACCGGATCGGCCAGCGGCGCGG

>NZ_CP011130|10|9|3461786-3461917|CRISPRCasFinder
GGACCGGTTCGGCCGGCTGGGCCG	GGCTGTCGGCCGCGGGTTCGCCGAGCAATTGCG
CGACCGGATCGACCAGCGGCGCGG	CCGGCTCGCTGCGGCGACGCAGCGAAT
CGACCGGATCGGCCAGCGGCGCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057921837.1|3465870_3466986_-|chorismate-synthase	unknown	unknown	gnl|CDD|235438
NZ_CP011130.1|WP_051547464.1|3464885_3465878_-|D-glycerate-dehydrogenase	unknown	unknown	gnl|CDD|240626
NZ_CP011130.1|WP_057921836.1|3463726_3464749_-|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|237845
NZ_CP011130.1|WP_160309479.1|3475093_3475258_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046656802.1|3460495_3461338_-|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl|CDD|234577
NZ_CP011130.1|WP_057921838.1|3467653_3468583_-|50S-ribosomal-protein-L3-N(5)-glutamine-methyltransferase	unknown	unknown	gnl|CDD|236988
NZ_CP011130.1|WP_046656809.1|3474413_3475097_-|lysoplasmalogenase	unknown	unknown	gnl|CDD|377946
NZ_CP011130.1|WP_057921834.1|3459836_3460499_-|phosphoribosylanthranilate-isomerase	unknown	unknown	gnl|CDD|234923
NZ_CP011130.1|WP_082648539.1|3450582_3451578_-|isopenicillin-N-synthase-family-oxygenase	unknown	unknown	gnl|CDD|226022
NZ_CP011130.1|WP_036108564.1|3449817_3450495_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057921841.1|3470441_3471509_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036115845.1|3454402_3455743_-|phosphoglucosamine-mutase	unknown	unknown	gnl|CDD|236787
NZ_CP011130.1|WP_057921829.1|3448251_3449415_+|hypothetical-protein	unknown	unknown	gnl|CDD|226119
NZ_CP011130.1|WP_057921839.1|3468920_3469565_+|SCO-family-protein	unknown	unknown	gnl|CDD|239266
NZ_CP011130.1|WP_057921840.1|3469561_3470410_+|phosphatidylserine-decarboxylase	unknown	unknown	gnl|CDD|234591
NZ_CP011130.1|WP_036115849.1|3456931_3457744_-|tryptophan-synthase-subunit-alpha	unknown	unknown	gnl|CDD|237285
NZ_CP011130.1|WP_036115852.1|3457940_3459167_-|tryptophan-synthase-subunit-beta	unknown	unknown	gnl|CDD|235288
NZ_CP011130.1|WP_057921842.1|3472270_3474346_+|bifunctional-diguanylate-cyclase/phosphodiesterase	unknown	unknown	gnl|CDD|236645
NZ_CP011130.1|WP_057921832.1|3451798_3453658_+|DUF3413-domain-containing-protein	unknown	unknown	gnl|CDD|225625
NZ_CP011130.1|WP_036115846.1|3455910_3456798_-|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta	unknown	unknown	gnl|CDD|235547

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057921837.1|3465870_3466986_-|chorismate-synthase	gnl|CDD|235438	PRK05382, PRK05382, chorismate synthase; Validated.	0
NZ_CP011130.1|WP_051547464.1|3464885_3465878_-|D-glycerate-dehydrogenase	gnl|CDD|240626	cd05301, GDH, D-glycerate dehydrogenase/hydroxypyruvate reductase (GDH). D-glycerate dehydrogenase (GDH, also known as hydroxypyruvate reductase, HPR) catalyzes the reversible reaction of (R)-glycerate + NAD+ to hydroxypyruvate + NADH + H+. In humans, HPR deficiency causes primary hyperoxaluria type 2, characterized by over-excretion of L-glycerate and oxalate in the urine, possibly due to an imbalance in competition with L-lactate dehydrogenase, another formate dehydrogenase (FDH)-like enzyme. GDH, like FDH and other members of the D-specific hydroxyacid dehydrogenase family that also includes L-alanine dehydrogenase and S-adenosylhomocysteine hydrolase, typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann-fold NAD+ binding form, despite often low sequence identity. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain. Some related proteins have similar structural subdomain but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence. While many members of this family are dimeric, alanine DH is hexameric and phosphoglycerate DH is tetrameric.	3.31807e-149
NZ_CP011130.1|WP_057921836.1|3463726_3464749_-|aspartate-semialdehyde-dehydrogenase	gnl|CDD|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP011130.1|WP_046656802.1|3460495_3461338_-|tRNA-pseudouridine(38-40)-synthase-TruA	gnl|CDD|234577	PRK00021, truA, tRNA pseudouridine(38-40) synthase TruA.	3.9923e-130
NZ_CP011130.1|WP_057921838.1|3467653_3468583_-|50S-ribosomal-protein-L3-N(5)-glutamine-methyltransferase	gnl|CDD|236988	PRK11805, PRK11805, 50S ribosomal protein L3 N(5)-glutamine methyltransferase.	1.2706e-156
NZ_CP011130.1|WP_046656809.1|3474413_3475097_-|lysoplasmalogenase	gnl|CDD|377946	pfam07947, YhhN, YhhN family. The members of this family are similar to the hypothetical protein yhhN expressed by E. coli. Many are annotated as possible transmembrane proteins, and in fact they all have a high proportion of hydrophobic residues. A human member of this family, formerly known as TMEM86B, is a lysoplasmalogenase that catalyzes the hydrolysis of the vinyl ether bond of lysoplasmalogen. Putative conserved active site residues have been proposed for the YhhN family.	3.67267e-36
NZ_CP011130.1|WP_057921834.1|3459836_3460499_-|phosphoribosylanthranilate-isomerase	gnl|CDD|234923	PRK01222, PRK01222, phosphoribosylanthranilate isomerase.	8.13649e-91
NZ_CP011130.1|WP_082648539.1|3450582_3451578_-|isopenicillin-N-synthase-family-oxygenase	gnl|CDD|226022	COG3491, PcbC, Isopenicillin N synthase and related dioxygenases [General function prediction only].	3.97845e-82
NZ_CP011130.1|WP_057921842.1|3472270_3474346_+|bifunctional-diguanylate-cyclase/phosphodiesterase	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	1.03441e-119
NZ_CP011130.1|WP_036115845.1|3454402_3455743_-|phosphoglucosamine-mutase	gnl|CDD|236787	PRK10887, glmM, phosphoglucosamine mutase; Provisional.	0
NZ_CP011130.1|WP_057921829.1|3448251_3449415_+|hypothetical-protein	gnl|CDD|226119	COG3591, COG3591, V8-like Glu-specific endopeptidase [Amino acid transport and metabolism].	1.73174e-08
NZ_CP011130.1|WP_057921839.1|3468920_3469565_+|SCO-family-protein	gnl|CDD|239266	cd02968, SCO, SCO (an acronym for Synthesis of Cytochrome c Oxidase) family; composed of proteins similar to Sco1, a membrane-anchored protein possessing a soluble domain with a TRX fold. Members of this family are required for the proper assembly of cytochrome c oxidase (COX). They contain a metal binding motif, typically CXXXC, which is located in a flexible loop. COX, the terminal enzyme in the respiratory chain, is imbedded in the inner mitochondrial membrane of all eukaryotes and in the plasma membrane of some prokaryotes. It is composed of two subunits, COX I and COX II. It has been proposed that Sco1 specifically delivers copper to the CuA site, a dinuclear copper center, of the COX II subunit. Mutations in human Sco1 and Sco2 cause fatal infantile hepatoencephalomyopathy and cardioencephalomyopathy, respectively. Both disorders are associated with severe COX deficiency in affected tissues. More recently, it has been argued that the redox sensitivity of the copper binding properties of Sco1 implies that it participates in signaling events rather than functioning as a chaperone that transfers copper to COX II.	8.32328e-49
NZ_CP011130.1|WP_057921840.1|3469561_3470410_+|phosphatidylserine-decarboxylase	gnl|CDD|234591	PRK00044, psd, phosphatidylserine decarboxylase; Reviewed.	1.81938e-174
NZ_CP011130.1|WP_036115849.1|3456931_3457744_-|tryptophan-synthase-subunit-alpha	gnl|CDD|237285	PRK13111, trpA, tryptophan synthase subunit alpha; Provisional.	9.73014e-124
NZ_CP011130.1|WP_036115852.1|3457940_3459167_-|tryptophan-synthase-subunit-beta	gnl|CDD|235288	PRK04346, PRK04346, tryptophan synthase subunit beta; Validated.	0
NZ_CP011130.1|WP_057921832.1|3451798_3453658_+|DUF3413-domain-containing-protein	gnl|CDD|225625	COG3083, COG3083, Predicted hydrolase of alkaline phosphatase superfamily [General function prediction only].	9.84511e-114
NZ_CP011130.1|WP_036115846.1|3455910_3456798_-|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta	gnl|CDD|235547	PRK05654, PRK05654, acetyl-CoA carboxylase carboxyltransferase subunit beta.	0

Protein sequences

>NZ_CP011130.1|WP_046656802.1|3460495_3461338_-|tRNA-pseudouridine(38-40)-synthase-TruA
MAVEQQQPQTSDGAAPVRRYALGVEYDGSEYSGWQRLVRPGEPDLRGEATVQTTLEQALSFVAGAPIDVTCAGRTDSGVHAACQVVHFDSPVEREPRGWVLGTTSRLPPSVCVRWCVPVAPGFHARFSARARRYRYRILNRPVRPALQRQYLTWERRPLDADAMHRAAQALLGEHDFSAFRTVHCQAPHARRDLQHIALRRDGEVVEMEVQANAFLHHMVRNIVGSLLLVGRGEQPETWIAELLAGRDRTVAGPTAPSSGLVFVGPRYPVECQLPAEVTL
>NZ_CP011130.1|WP_057921834.1|3459836_3460499_-|phosphoribosylanthranilate-isomerase
MSQPRTLFRTRIKFCGFTRPGDVRLACELGADAIGFVFAAGSKRRVAPEEARAMRQALAPLVDAVALFSDNPVDEVREVVRQVRPSLLQFHGNEDDAFCRGFGVPYLKAIPMGGELADQHPSALHMRYPGAAGFLFDSHAHGGSGGSGKTFDWKRIPVGVQKPFVLAGGITLDNVFEAILATLPWGVDVSSGIESAPGLKDGDKMRHFVEQVRKADCHVD
>NZ_CP011130.1|WP_036115852.1|3457940_3459167_-|tryptophan-synthase-subunit-beta
MSAEPIAPPIDFHAYPDANGHFGRYGGRFVAETLIAPIEELAKAYDAARVDPAFIKEFENDLAHYVGRPSPIYHAQRLSDEVGGARILLKREDLNHTGAHKINNTIGQALLASRMGKTRIIAETGAGQHGVASATVAARLGLECVVYMGATDIERQKINVYRMKLLGATVVPVTSGSQTLKDALNEAMRDWVTNVRDTFYIIGTVAGPDPYPRMVRDFNAVVGREARAQMLAEYGRLPDAITACVGGGSNAIGLFHAFLNDPSVRIVGAEAAGDGIDTGRHAASLAAGRPGVLHGNRTYVLCDDDGQIIETHSVSAGLDYPGVGPEHAFLKDTGRAEYLGITDEEALDAFRTLARTEGILAALESSHAIAQAIKLARTMPKDQVVLCNLSGRGDKDVHTIAGREGLHF
>NZ_CP011130.1|WP_036115849.1|3456931_3457744_-|tryptophan-synthase-subunit-alpha
MNRIDAKFQHLHAAGRKALIPFVTAGDPSLEATVPVMHALVEAGADVIELGVPFSDPMADGPTIQRSSERAIARGAGLSWVLEAVREFRGRDADTPVVLMGYLNPIEIRGSTRFADDAVAAGVDGVLLVDLPPEEAAELRAAFAAAGLALILLASPTTTEERIALLCDDAQGYLYYVSFAGVTGAADLLDTGAANDRLHRIRARSKVPVVAGFGIKDAASAATMAREADGVVVGSALVAVLAETADAAAAAQAAGAFLAPLRQALDGAAG
>NZ_CP011130.1|WP_036115846.1|3455910_3456798_-|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta
MSWLKKLMPSGIRTETVAAKRRSVPEGLWEKCDRCGAVLYRPELEENLEVCPKCSFHMPIRGRVRLNALFDPGSTVEIGAELGPVDVLKFKDQKKYSERIKAAQKATGERDALIAMRGTLKQRPLVAASFDFAFMGGSMGSVVGERFTLGAETALQIGSPFVCFSASGGARMQESLFSLMQMAKTSAALGRLRAAGLPYISVMTHPTTGGVSASFAMLGDINMAEPEALIGFAGPRVIEQTVREKLPEGFQRSEFLVDHGAVDQICDRRELRDRLAHLLAMMMKQPQPEDDVEAA
>NZ_CP011130.1|WP_036115845.1|3454402_3455743_-|phosphoglucosamine-mutase
MTRKYFGTDGIRGRVGEGAISADFVLRLGNAYGHALIRRGWRNPMVIIGKDTRISNYMFEAALEAGLVAAGVDVQLMGPMPTPAVAHLTRSLRADGGIVISASHNPHYDNGIKFFSAEGEKLDDETELAIEAALEEPFRTVESERLGKAVRTRDAIGRYLEACKNSVPRGFDLSGMRIAMDCANGATYQTGPLVLRELGARVDAIGIDPNGLNINDGVGSTHPQTLVERVQATGADLGIAFDGDGDRVLFVDGEGRICDGDDLLYVLATDWQRSGRLQGPVVGTLMTNYGLERAFEQRGIGFLRAKVGDRYVHQQLIAHGGTLGGEASGHLLCLDRTSTGDGIVSALQVLEVLGRTGLTLRQALDGLSRVPQKTVNVRFEGTSKPTEAASVKEALKQAEAAVAGHGRAFLRPSGTEPVVRVTVEADDATLMQNTLDSLAAAVRAAV
>NZ_CP011130.1|WP_057921832.1|3451798_3453658_+|DUF3413-domain-containing-protein
MQDPAARPATPARRALAWLTGFTLGNAAVAIAIAASNIPFAHLAEHWKAAFFLTLALPGHFVFFGALLGLIPLLLGRLSRRASWMTVAAVVLQTAWLCLLVADAKVFALYRFHLNAMVANMVFGGAMQDQVVFSGTVWGLIALAIATVLALEIAAAWLCWRWIERRPGAVKILRAWWVALAVMLFGQAMIAYYDARGDRAVLSQLPYIPWAQPITLKDSLHRFGVKNNPNSALPVLGSGLLAYPRKPLDCEAAPKLNVVVILLESLRHDALDPTVMPNTWRYAQQSQWFDDHYSTGNATRFGLFGLLYGLPGGYWHPMLAEQRGSAFIGQMKKDGYAMHIYGSAPLYNPEFDRTVFSEVRNHVVNGPRERHSAERDRAIIDRLRGDLAATRPEQRFFGFVFLDSPHQPYYMPKGYPPLFKPMADSINPLEFGPDHDPIPDFNRYRTAVHYSDSLIGDFLASLRASPFADNTVVLITGDHGEEFNDLKQNYWGHNGNFSDYQLRTPFVLHWPGKPPRKFIHTTSHQDFVPTVMQHALGCRNDPNDYSTGRDLFGPAQTARPMLVESWSQRGIRQGDRIYLFDNYGAATVVDRNYRPLPDAKVDPAAVSQSWEMLTRFQQR
>NZ_CP011130.1|WP_082648539.1|3450582_3451578_-|isopenicillin-N-synthase-family-oxygenase
MAALSEDSGLFGRDTNRTSHVSQIPTLDIRRFDTDREAFVVELGAAYREWGFAGINGHGIPAEQIDQSYDVFKRFFALPEEVKRKYHVPGGGGARGYTPFGVETAKGAKHFDLKEFWHVGREIPRDSKYAAEMPANLWPDEIPEFREQAYGLYTTLDQLGSRVLSALALHIGLPQTYFADKTDFGNSILRPIHYPPITADDIPNERAGAHEDINLITLLVGASAAGLEVKSRKGEWVPFTADADTIVVNIGDMLQRLTNHVYPSTTHRVVNPPGEKARQPRYSTPFFLHPNPDFLIDVLPSTISADNPSRYPEPITAQGYLEERLREIKLK
>NZ_CP011130.1|WP_036108564.1|3449817_3450495_+|hypothetical-protein
MKPIPPRPLLPILPYRKPTPGRDYWVVDDVLPDPDGVRARFLAKTDWSQGYPYKPESWPGQRAMPGLSDEELAIVETRVREALGATRLWVGAAPDGQTLNHNCVQVVGIDECEPRPHTDSRTMCRYAAVLYLNPSVPDHCGTGFYRQRLGNGQRGGNTVSPPHANLVEALGTRFVAPDAFVEDVVVPHRYNRLLLYRANLIHSASGYWGRTLDTMRMAAVFFWMV
>NZ_CP011130.1|WP_057921829.1|3448251_3449415_+|hypothetical-protein
MKSHRINPPCRLSRKLALLSGIALLSSAALAMAGEKVIRTAYGDVASIDAPKSQQLNAKSAQAHPFATARQRAAAKPVIWVDRDSKAGPAASAELTDKLIRTAGSAPGGDAPAFGNYLARTHFRATWDKLDALDARQGAAPDVSISQEKDGAHYGYTRTLGNYYTTQWKAAPWNKIGKLYFTKPNGSSSYCTAQVSSGTAVLTTAAHCVYTFGSGWNSNFLFVPAERYGEAPYGKFGWSTARVPTNWINQGTRRWDVAVIKLTGEQVSGIPVTSYVGWLGRAWNQPYSLFTYSHGYASNLSTQYTNICAGQTYDSPSEGTNVVVQGCDMTYGASGGAWLINYTPNSSAGNQVNSVVSGPHIGAFGTAWVGARFNDDNIVALCTAIGC
>NZ_CP011130.1|WP_057921836.1|3463726_3464749_-|aspartate-semialdehyde-dehydrogenase
MNAKTSCNVAVVGATGAVGETMLKVLAERKFPIGKLHVLASERSAGEKLEYEGKTIVVEDLALFDPSGVDIALFSAGGSVSKQYAPKFAAAGAVVIDNSSAFRYDDDIPLVVSEVNPEAARNRPRGIIANPNCSTMQMLVALAPIHRQARIERINVATYQSVSGTGKRAMEELGKQTAALLSFQQIDPQVYPVQIAFNVIPHGGDFTDNGYTTEEMKLVWETRKILGDDSIGVNATVVRVPVFYGHSEAVHIETRDKLSAADARALLEKAPGVVVVDEPVNGGYPTPVTHASGQDPVFVGRIREDISHPRGLSLWVVSDNIRKGAATNAVQLAELVWNER
>NZ_CP011130.1|WP_051547464.1|3464885_3465878_-|D-glycerate-dehydrogenase
MSERPRVWVSQPLFDDVIARLDEYFEVSATTAVTQHAPEAVAAALREADGALVTLNDPIGAAQIAGATRLRAIANVGVGYNNLDLPALSAAGILATNTPDVLTETTADFGWALMMATARRISEAERWLREGHWQRWSFDSLLGGDVHGSTLGILGMGRIGQAIARRAAGFGMRTLYHNRSRLPEAVERECAAGYVSFDELLGRADHLILVLPYSPQSHHLIDAAALAKMQAQATLTNIARGGIVDENALCDALEQGRLAAAGLDVYEGEPRLNPRLLEQRRVVLTPHIASGSLATRRAMVSLAVDNLIAALGHGPNAGKPPSLLNAGIRD
>NZ_CP011130.1|WP_057921837.1|3465870_3466986_-|chorismate-synthase
MSSNSFGKLFTVTTFGESHGPAIGCVVDGCPPGLSIAPEDFRHDLDRRATGKTRHTSARRETDDIEILSGVFEGRTTGTPIALLIRNTDARSKDYGSIAEQFRPGHADYSYWQKYGLRDPRGGGRSSARETTMRVAAGVIAKKWLAERFGVVVRGFMSQIGEVVPNGYDLSVVESNPFFWPDAAQVAELETYMDALRKSGDSVGARVDVIADNVPPGWGEPIYGKLDGELAAALMSINAVKGVEIGDGFASVASKGSAHRDEISLQGFASNHAGGILGGISTGQQLRCSTAFKPTSSLRLPGRSVDIHGNEVEVITTGRHDPCVGIRATPICEAMVALVLIDQALRHRAQCGDVGTITPRIPATPEFDGDV
>NZ_CP011130.1|WP_057921838.1|3467653_3468583_-|50S-ribosomal-protein-L3-N(5)-glutamine-methyltransferase
MPASVSFESLTLVDLIRYGASRFSAAGLTFGHSYDNALDEATQLVLHALHLPHDLSPVYGQGKVTTEEKDAVLALFERRIGERIPAAYLTGEAWFAGLSFKSDSRALVPRSPIAELIESGFEPWLGGREVERALDLCTGSGCIAIATAHYHPDWQVIGADINDAALSLAVENKERLHTGNVELRKSDLFQGLQGEVFDLIVTNPPYVTNDETDALPREYSHEPELGLRAGDDGLDLALKILRDAPDHLSEHGVLICEVGEAERALVELLPQLPLAWVEFKVGQMGIFVAERHDLVEHHDAIKRLADARA
>NZ_CP011130.1|WP_057921839.1|3468920_3469565_+|SCO-family-protein
MFNRTTAIVLIAALAAALGLWASQKYFGSVRHASLPQTEAVRLIEPRRTLPAFSLRQSDGTQLIPGELKGHWTLVFLGFTHCPDVCPTTLAQMSVAQKAWESIPEATRPRVLFVSVDPERDTPDKIGEYAHGFHKDTLAATADVPALESFAKSLSMVFAKVPAPDGAPADQYTLDHSASMVVLDPQGRMAGLLRPPFDPNVIAKDMAMLTEAAP
>NZ_CP011130.1|WP_057921840.1|3469561_3470410_+|phosphatidylserine-decarboxylase
MSLVTTLTYVLPHRLMSSLARALAYSDRPGVSRWLIDTVTRKFGVDLGEAANSDPRSYPTFNAFFTRALKPGARVPDPDPRVLLMPADGRISQCGPIRDGEIFQAKGQSFTATELLGGDEAAAAPFRDGVFATVYLSPKDYHRVHMPWAGTLRETVHVPGRLFSVGPDAVRNVPRLFARNERLVCHFDTEFGPMAMVMVGALLVSGVETVWSGVEIPRYGDIVTTKDYRGEAVTLERFAEMARFNYGSTVIVLLPPGVAALDPGLGAETAVRLGQALARRSD
>NZ_CP011130.1|WP_057921841.1|3470441_3471509_+|hypothetical-protein
MPSTHRPALRRAALTATVALLTLALAACGSKSETEQLAELRDGIAYTQYRRLSENGLPGGLTAYQKGLHWTGENWASNNPTADLPKGDFSEADLCVVHVLVAYSALIANKNTIALAESDIVEAQSCGAFDRAAATSLRAVVFQREQWPGLAKLEGEKAWELPTQAGEDLPPAEHVMVLHAALAYFAASEQEWERAQVHFDALGHLLGQPWFAQIPPVGIAFKEGRTRDGLSAIKKLSVDPSAPAEVRKELVALIAKVEAKGGDVDSAIFMPRLVATLTWEMIAAEGPQLLRTATGFAEEQADWAALSDSVKDGTGKAKATAAQWWNKAREAVSSPNQTPADDTTDAPAETDARSR
>NZ_CP011130.1|WP_057921842.1|3472270_3474346_+|bifunctional-diguanylate-cyclase/phosphodiesterase
MLQGIYSGYLVAISYVVAALASYVALQLAGRATHGDGAARWWWRIGGGCAMGFGIWSMHFIGMLAFQLPIPLGYDLLKTFSSLIAACIASSFALWLVTQRELPPLRHALGAVLMGGGIAAMHYTGMAAMEMNPGIVWNRFWFVLSIVVAVVAAGTALWIAFRLRGESRDAWRMRIVAAMVMGLAVTGMHYTGMEAAGFPEGSICTAAGPNGMPVKWLATLVTIAAFAILAIALMTAVLDRRLQERTSRLRFSLGKAKDQLVFLALHDNLTRLPNRVLLEDRIDEAVQKSARSGARFAVMFLDLDGFKAVNDVYGHHMGDRLLREVAARLTAALRAQDTVARIGGDEFVVVMELGEPADAAIVAGKLIGVMSADFHIDGTQIRVSGSLGIAIHPQDGADGRELLTNADAAMYHAKEHGRNGFRFFEPSMNEGVREQLSLMQDLRHAMERNEFALHYQPKYGAPNGPLIGAEALLRWYHPTRGIVPPEHFIVLAEKSGTLVKLDAWVLNEACRQLRVWHDAGLVLAGISVNLSPAQFESTELFDLVRDVLARHRLEPGALTLEVTESTAMKDPESSLVILRRLSELGVRISIDDFGTGYSSLLYLKRLPARELKIDRGFIRDLSQGTEDAAIVSAIVELGRMLDLKIIAEGVETTAQAGLLADLGCDSLQGYLFSHPLPPDDFMALVAREPVH
>NZ_CP011130.1|WP_046656809.1|3474413_3475097_-|lysoplasmalogenase
MNQTIDDAVTVPRAWLATVAVAAVLAIVGAYASPWLHYLFKPLTTLLIVAMVWRHGGAAEPAYRRAIVIGLLLSTCGDVFLMLPGDWFVFGLGSFLCAHIAYLIGLTRRARLFARVWPYLAYALLAGAVLSVLWAHLPGDLRIPVIVYVAVLAAMAAQAAVVWRCARSRSTALAALGGAFFVASDATLAIDRFAAPFGAASAVVLATYWIAQLLIGSSVRHSGQRRT
>NZ_CP011130.1|WP_160309479.1|3475093_3475258_-|hypothetical-protein
MGADNSGLASTLKSEARLRERIAAIIDEAGIGPDTGAGATPVRGPVAITQDAGA

Crispr_ID: NZ_CP011130_11

• CRISPR_ID: NZ_CP011130_11
• CRISPR_location: 3956132-3956288
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_11

Consensus_repeat	Method
CACGGCGCACATCCATGTGCGCCGCCCTTCGGGTGTGCTTTTGTTCTCGCGAGT	CRISPRCasFinder

spacers of NZ_CP011130_11

>11.1|3956186|49|NZ_CP011130|CRISPRCasFinder
TCCGGGCTTCGCAGCGCTGGATGACCTACGCGGCTTCAAGCCCAAGCCA

CRISPR arrays and Neighbor proteins around NZ_CP011130_11

CRISPR arrays

The CRISPR arrays of NZ_CP011130_11

>merge|NZ_CP011130|11|3956132-3956288|CRISPRCasFinder
CACGGCGCACATCCATGTGCGCCGCCCTTCGGGTGTGCTTTTGTTCTCGCGAGTTCCGGGCTTCGCAGCGCTGGATGACCTACGCGGCTTCAAGCCCAAGCCACACGGCGCACATCCATGTGCGCCGCTCTTCGGGTGTGCTTTTGTTCTCGCGAGT

>NZ_CP011130|11|10|3956132-3956288|CRISPRCasFinder
CACGGCGCACATCCATGTGCGCCGCCCTTCGGGTGTGCTTTTGTTCTCGCGAGT	TCCGGGCTTCGCAGCGCTGGATGACCTACGCGGCTTCAAGCCCAAGCCA
CACGGCGCACATCCATGTGCGCCGCTCTTCGGGTGTGCTTTTGTTCTCGCGAGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057922088.1|3944137_3945667_+|exopolyphosphatase	unknown	unknown	gnl|CDD|223326
NZ_CP011130.1|WP_057923605.1|3964432_3964924_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379326
NZ_CP011130.1|WP_057922092.1|3949315_3949930_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036109243.1|3961481_3962153_-|two-component-system-response-regulator-CreB	unknown	unknown	gnl|CDD|236838
NZ_CP011130.1|WP_057922099.1|3964908_3965922_-|DUF1963-domain-containing-protein	unknown	unknown	gnl|CDD|370378
NZ_CP011130.1|WP_148650447.1|3946240_3946789_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922098.1|3960028_3961471_-|two-component-system-sensor-histidine-kinase-CreC	unknown	unknown	gnl|CDD|236846
NZ_CP011130.1|WP_036109252.1|3963681_3963882_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046657281.1|3962342_3963203_+|23S-rRNA-(adenine(2030)-N(6))-methyltransferase-RlmJ	unknown	unknown	gnl|CDD|225509
NZ_CP011130.1|WP_057923604.1|3956431_3957316_-|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl|CDD|143598
NZ_CP011130.1|WP_057922095.1|3953713_3954901_+|glycosyltransferase-family-1-protein	unknown	unknown	gnl|CDD|340842
NZ_CP011130.1|WP_057922096.1|3954897_3955449_+|phosphatase-PAP2-family-protein	unknown	unknown	gnl|CDD|239486
NZ_CP011130.1|WP_036109254.1|3964146_3964371_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922094.1|3951958_3953479_-|glucan-biosynthesis-protein	unknown	unknown	gnl|CDD|377321
NZ_CP011130.1|WP_057922093.1|3950042_3951962_-|glucans-biosynthesis-glucosyltransferase-MdoH	unknown	unknown	gnl|CDD|235476
NZ_CP011130.1|WP_057922090.1|3946841_3947153_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922097.1|3957315_3957921_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|173926
NZ_CP011130.1|WP_082648586.1|3958134_3959586_-|cell-envelope-integrity-protein-CreD	unknown	unknown	gnl|CDD|236960
NZ_CP011130.1|WP_036112076.1|3942042_3944127_+|polyphosphate-kinase-1	unknown	unknown	gnl|CDD|235469
NZ_CP011130.1|WP_057922091.1|3947279_3948998_-|AMP-binding-protein	unknown	unknown	gnl|CDD|236236

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057922088.1|3944137_3945667_+|exopolyphosphatase	gnl|CDD|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	9.26594e-155
NZ_CP011130.1|WP_057922093.1|3950042_3951962_-|glucans-biosynthesis-glucosyltransferase-MdoH	gnl|CDD|235476	PRK05454, PRK05454, glucans biosynthesis glucosyltransferase MdoH.	0
NZ_CP011130.1|WP_036109243.1|3961481_3962153_-|two-component-system-response-regulator-CreB	gnl|CDD|236838	PRK11083, PRK11083, DNA-binding response regulator CreB; Provisional.	4.68557e-124
NZ_CP011130.1|WP_057922099.1|3964908_3965922_-|DUF1963-domain-containing-protein	gnl|CDD|370378	pfam09234, DUF1963, Domain of unknown function (DUF1963). This domain is found in a set of hypothetical bacterial proteins. Its exact function has not, as yet, been described.	6.10804e-60
NZ_CP011130.1|WP_057922091.1|3947279_3948998_-|AMP-binding-protein	gnl|CDD|236236	PRK08315, PRK08315, AMP-binding domain protein; Validated.	0
NZ_CP011130.1|WP_082648586.1|3958134_3959586_-|cell-envelope-integrity-protein-CreD	gnl|CDD|236960	PRK11715, PRK11715, cell envelope integrity protein CreD.	6.86912e-177
NZ_CP011130.1|WP_046657281.1|3962342_3963203_+|23S-rRNA-(adenine(2030)-N(6))-methyltransferase-RlmJ	gnl|CDD|225509	COG2961, ComJ, Protein involved in catabolism of external DNA [General function prediction only].	1.07013e-108
NZ_CP011130.1|WP_057923604.1|3956431_3957316_-|carbon-nitrogen-hydrolase-family-protein	gnl|CDD|143598	cd07574, nitrilase_Rim1_like, Uncharacterized subgroup of the nitrilase superfamily; some members of this subgroup have an N-terminal RimI domain (class 12 nitrilases). Some members of this subgroup are implicated in post-translational modification, as they contain an N-terminal GCN5-related N-acetyltransferase (GNAT) protein RimI family domain. The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), this subgroup corresponds to class 12. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	1.45736e-111
NZ_CP011130.1|WP_057922095.1|3953713_3954901_+|glycosyltransferase-family-1-protein	gnl|CDD|340842	cd03814, GT4-like, glycosyltransferase family 4 proteins. This family is most closely related to the GT4 family of glycosyltransferases and includes a sequence annotated as alpha-D-mannose-alpha(1-6)phosphatidyl myo-inositol monomannoside transferase from Bacillus halodurans. 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 bacteria and eukaryotes.	1.33347e-126
NZ_CP011130.1|WP_057922096.1|3954897_3955449_+|phosphatase-PAP2-family-protein	gnl|CDD|239486	cd03392, PAP2_like_2, PAP2_like_2 proteins. PAP2 is a super-family of phosphatases and haloperoxidases. This subgroup, which is specific to bacteria, lacks functional characterization and may act as a membrane-associated lipid phosphatase.	1.47166e-16
NZ_CP011130.1|WP_057922094.1|3951958_3953479_-|glucan-biosynthesis-protein	gnl|CDD|377321	pfam04349, MdoG, Periplasmic glucan biosynthesis protein, MdoG. This family represents MdoG, a protein that is necessary for the synthesis of periplasmic glucans. The function of MdoG remains unknown. It has been suggested that it may catalyze the addition of branches to a linear glucan backbone.	0
NZ_CP011130.1|WP_057923605.1|3964432_3964924_-|GNAT-family-N-acetyltransferase	gnl|CDD|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	0.000771506
NZ_CP011130.1|WP_057922098.1|3960028_3961471_-|two-component-system-sensor-histidine-kinase-CreC	gnl|CDD|236846	PRK11100, PRK11100, sensory histidine kinase CreC; Provisional.	0
NZ_CP011130.1|WP_036112076.1|3942042_3944127_+|polyphosphate-kinase-1	gnl|CDD|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP011130.1|WP_057922097.1|3957315_3957921_-|GNAT-family-N-acetyltransferase	gnl|CDD|173926	cd04301, NAT_SF, N-Acyltransferase superfamily: Various enzymes that characteristically catalyze the transfer of an acyl group to a substrate. NAT (N-Acyltransferase) is a large superfamily of enzymes that mostly catalyze the transfer of an acyl group to a substrate and are implicated in a variety of functions, ranging from bacterial antibiotic resistance to circadian rhythms in mammals. Members include GCN5-related N-Acetyltransferases (GNAT) such as Aminoglycoside N-acetyltransferases, Histone N-acetyltransferase (HAT) enzymes, and Serotonin N-acetyltransferase, which catalyze the transfer of an acetyl group to a substrate. The kinetic mechanism of most GNATs involves the ordered formation of a ternary complex: the reaction begins with Acetyl Coenzyme A (AcCoA) binding, followed by binding of substrate, then direct transfer of the acetyl group from AcCoA to the substrate, followed by product and subsequent CoA release. Other family members include Arginine/ornithine N-succinyltransferase, Myristoyl-CoA: protein N-myristoyltransferase, and Acyl-homoserinelactone synthase which have a similar catalytic mechanism but differ in types of acyl groups transferred. Leucyl/phenylalanyl-tRNA-protein transferase and FemXAB nonribosomal peptidyltransferases which catalyze similar peptidyltransferase reactions are also included.	0.00122441

Protein sequences

>NZ_CP011130.1|WP_057922096.1|3954897_3955449_+|phosphatase-PAP2-family-protein
MNRLPLRKRLIAGESGWCLRANRLGERNSSRAYFAAVSRLGDGVFWYALMAALIVADGYDGLRASLHLAATGVIALALYKLLKRWTRRPRPFASDQRIHAWVAPLDEFSFPSGHTLHAVAFSLVAMAHYPVLAWLLIPFTASVAASRVVLGLHYPSDVVAATVIGSSLAGFSLWLVPGVTLFG
>NZ_CP011130.1|WP_057922095.1|3953713_3954901_+|glycosyltransferase-family-1-protein
MRYAIVTETYPPEINGVALTVQGLEQGLRARGHEVGLVRPRQLGDGAQAQPHELLVNSLPLPRYPGLRFGLPCAGRLRAAWTRDRPDAIYVATEGPLGWSALRAAKRLGIPAATGFHTRFDEYMRDYGAPFLAGTALAWMRRFHNGADATLVPTRELAEFLRSRGFEDVVRLPRAVDTQLFDPRRRSAALRRQWGLDDDGFAAIYVGRIAAEKNLELAVRAFRALQRQRPQARFVWVGDGPAREKLQRDHPDFIFCGVQRGDVLAEHFASGDLFVFPSHSETFGNVTLEAMASGVPTVAFDYGAAREHLRDGLHGAAIADGDDAGFIEAAVRIGSQDALRAGMSRAGRDAISGLRPAQVAADFDALLHALAQRNPRNRNIPASQRDKPKPKQEVV
>NZ_CP011130.1|WP_057922094.1|3951958_3953479_-|glucan-biosynthesis-protein
MQRRELLQAGLTLPLAALAGGGWLPALAAAGPAQRFDAGTVPALARALAAKAYRPADADLPEALARIKYDTWRDIRFDPAQALWKKDGLPFQVQFFHRAFLFKHRVDMHLVHGGQATPVVYRPQMFDFGKAPKPAQDDLGFAGFRLHAPINRKDYFDEVCAFLGASYFRAVAKDLLYGLSARGLALNTGAGGDEEFPVFTGFWIEQPAAGAKQIVVHALMDSPSVAGALRFAITPGTQTVFDTQLRLYPRVALDRVGIAPLTSMYHFDATDRVGIDDFRPAVHDSDGLAMHNGAGEQIWRPLHNPGSLQESAFQDRSPRAFGLMQRKRAFADYADSEAHYERRPSLWVEPVGDWGEGAVHLIEIPTKDEYHDNMVAFWRPRAPLAAGREHRFDYRLHWCAEHAWAPTLATVRRTRIGAGGDGARLVVIDLDGGRLRALAADAQPRAVVWASSGRVVNALAHANAGTGGWRMSFELQPGDARVVELRAVLEDARGPLSETWLYRWTA
>NZ_CP011130.1|WP_057922093.1|3950042_3951962_-|glucans-biosynthesis-glucosyltransferase-MdoH
MNATVAPPKTTPAVAYEALPAEAPMAMPVQSLRVGERPDRPLPSAPNAMGWRRLYVIGGAALLTLTAGYHILRVLYVGGLSLLEGMLLVLFVPLFAWIALAFTSSLAGFCLILSRRRWRFGLKQGGELPVLGQRTALLMPTYNEDPERLMAGLQAIYESVVATGQVDRFDFFILSDTTKEPIRQAEIRAFLALRERTGEHERIFYRRRKNNDERKAGNIAEWVRRFGAAYPQMLILDADSLMTGEVIVKLSGAMERNADVGLIQTLPMIVNGQTLFARMQQFAGRVYGPVIAYGIAWWHGAESNYWGHNAIIRTQAFADHAGLPELRGYKPFGGTVLSHDFVEAAFMRRGGWALHMVPGLVGSYEEGPPSLTDMLVRDRRWCQGNLQHGAVVSAKGLHWISRMHMAMGIGHYFTAPMWAMLMLIGLAIPLDKEGFFNWVSIRLPGFSPSAYWRDQDPDRVLWVFVATMAVLLAPKFMGFLAMLTDRETRRGCGGAIRAFLSMIFETLLAALMAPITMYVQSRGVAEVLAGKDSGWESQRRDDGSLPLSGLIRSYGGLSLLGVLIGGMAYVVSPPLAAWMSPVIIGLVLSIPVVAFTSARSTGLWLRKIGIFRIPEEITPPPVLVRAKQLRAEAAQRGAS
>NZ_CP011130.1|WP_057922092.1|3949315_3949930_+|hypothetical-protein
MSIVHPLSRLALSLLVPIALAMPAQAKQPATRAPAAAQTQSAASLNFNGARYLHRWSDSTQAEFTPAGQEDLSKWQDMITVVTNAGARDGEQLAGLAEAVLARYKQAGKIIKTDSKPRTPQSPAEHLIVAVLPGKGFVETVFARIKLIDDTGTIAIYAHRVYGENAANDFGAWLTANGEATERAVMAWDGIPTPAQLSALPRSK
>NZ_CP011130.1|WP_057922091.1|3947279_3948998_-|AMP-binding-protein
MNAAHAAPDPALSHVVGAATPPLLDETIGAMLSRIAAIWPERDALVVPPQGVRMNWREFDAAVDRLAAGLLKLGLAPGDRIGVWSLNRAEWVLLQFASARVGLILVNINPAYRTHELEYALNLVACRALAIVPSFKTSHYLQMLRELAPELGQHPPGLLRARRLPDLRHVLTMGSGEPPAGTHAFDAIAACEDPDAHARLEQIAAQLSPDDAVNIQFTSGTTGAPKGATLTHRNIVNNGFFVGEAMRLSERDRLCIPVPFYHCFGMVLGNMACVTHGACMVIPGEGFDPLVTLQTVADERCTGLHGVPTMFIGELEHPRFGEFDLSSLRTGIMAGSNCPIEVMKQVVERMHMQQVTIAYGMTETSPVSFQTVPDDPLARRVDSVGRVHPHVEVRVVDEDGNTVPRGEIGELLTRGYSVMQGYWGDPKRTAEAIDSEGWMHTGDQAVIDADGYAHIVGRLKDMLIRGGENVYPREIEEFLYAHPAIADVQVFGVPDAKFGEEVCAWIRLADGAALDADAVRAFCQGRIAQYKIPRYIEFVDSLPMTISGKPQKFVMREKMIERLSMSANSSGG
>NZ_CP011130.1|WP_057922090.1|3946841_3947153_+|hypothetical-protein
MKTILTTLAAALLAVSGSASAEFIETTEISQIGAYQAATTHYVWLSTGISAECAAQGTNSVLAFDEAQPGGKGLLAILTSALLNKRKVSVRTSGCNIVEVYLK
>NZ_CP011130.1|WP_148650447.1|3946240_3946789_+|hypothetical-protein
MFRYLIFALAVLHSGGALAVGCKEAPRFGNSPTVTVLNASPENPRPGDEITLTALVEAADVFSVSCQNPDHSVQRIGGIIDVFAGATRIGSVQIAPENTHQVYLGTYYDPACPQGFTCPFFYYGFNTTSYSVKFRMPMDSTQQTFTASFSGDKHFSRGSNSQPLNMSAAYADNSPIISYLLN
>NZ_CP011130.1|WP_057922088.1|3944137_3945667_+|exopolyphosphatase
MNNLFPTTRLPLQDGDLLAAIDLGSNSFHMVVARYVLGQLRTVDRLRETVRLAEGLDRKGGLAPDVRQRALECLSRFGQRIRDVPPQRVRAIATNTVRRLAAPQAFLMPAESALGHAIEVVSGREEARLIYLGIAHAQPSKPGERRLVIDIGGGSTECIVGSGFEAIERESLQVGCIATTRRFFENGKLSKKKWRDALTEVSAEFQQFAGTYRALGWHEALGSSGTNKAIGEICAAMKLTKGAITAEALPQLRDRLLQADRIEAIDLPGLSADRRPVIAGGILILEAAFNVLGLQRMAISKAAMREGVLYDMLGRGGADDPRDAAVVALVKRYGIDEQQSARVEATMLRLFDQVAKAWNLDADDRLMLQRATRLHELGLVIAHSQYHVHSSYVLENSDISGFSRQQQQFLAALVRTHRRGIPKNAFDALPDRLLAAVRRSSALLRLAVLLHRAHESDPIPQLDAHADGNTLTLTVSKRWLESRPLIRADLEGEPQDMAGLGIALKLLAA
>NZ_CP011130.1|WP_036112076.1|3942042_3944127_+|polyphosphate-kinase-1
MNAMTDTSLDTDPLRDSALYFNRELSQLDFNFRVLAQAQDPQVPLLERLKYLCISCTNLDEFFEIRAGTLRHAQDLGLAPGPDGLAPQTVLSRIHDRAAELVKAQYECWNDVLRPALQESGVRVLGRNSWNARQTRWLRAYFRDEIMPVLSPLGLDPAHPFPKILNKSLNIVVVLKGKDAFGRAGNLAIVRAPRSLPRIIQMPENVSGGKHDFVFLSSVLSAFVDELFPGMEVKGAYQFRVTRNSELLVDEEEVDNIALALRDELIGRGYLRAVRLEIAEQCPKPIVRTLLENFDLPENAVYRINGPVNLNRVIQVYDLVQRPELKFPPYQQRVLPGVDTLFDTVAEGDVLLHHPFDSFAPVLELIRQSAEDPNVLAIKQTLYRAGKDSPIVEQLVQAARNGKDVTVVVELRARFDEEANLGLADRLQEAGVQVVYGVVGYKTHAKMLLIVRREGRKLKRYVHLGTGNYHSGTARAYTDFGLITADPDIGNDVHMIFQQLSGLAPSLKLKCLLQSPFTLHAGVLKRIDRETKHARAGKPARIVAKMNALNEPQVIRALYQASQAGVQIDLIVRGACTLRPGVEGISDNIRVRSIVGRFLEHHRVYWFANDGAPDLFCSSADWLERNLLRRVETGFPILDTDLRARVYDEALANYLADNLNAWELQADGHYSRVLPRDGEMPHSAQSTLLAKICG
>NZ_CP011130.1|WP_057923604.1|3956431_3957316_-|carbon-nitrogen-hydrolase-family-protein
MRVAVAKYAIGAPRTFAEFADKQTQWLSEARRSGAQLAVLPEYLSLELGATFGAATQGDLHASLVATQAYHGAWLDFFGLLARELGLHIVAGSFLFDPGHGRYRNRSYAFAPDGGCLWQDKLQLTGFEKQAGVIEAGDALKTFALGEQRAGIAICYDIEFPLPVRAQCEAGARLLIAPSCTDTAAGATRVRVGCLARALENRCFVAQAVTAGEALWSPALDTNTGEAAVYAPMDVGLPADGVLAQTRGGQRWAYADLDFVALEASRARAQVANDRDWVGQLRPGVLRAQVDRFG
>NZ_CP011130.1|WP_057922097.1|3957315_3957921_-|GNAT-family-N-acetyltransferase
MKKPMPEIRSYAGAEITPYLEAIAALRIAVFRDWPYLYDGDAAYEAKYLQTYRDSWRSIAVLAFDGPRVVGASTGVPMSDEIPEFRAAFDDHLLDVDHVFYCGESVLLPEYRGRGVGHRFFDMREAHARALGGFNWTTFCAVEREPDDPRQPPFHRGNEVFWKKRGYTRRPELRANLPWNEVGRGEREHTLSFWLRPLGRA
>NZ_CP011130.1|WP_082648586.1|3958134_3959586_-|cell-envelope-integrity-protein-CreD
MRVWLKMLMVLGMTLAILIPLLMIGGIISERQQYRAQAVATVARSYAGAQAFSGPALVVPYEDTWVEAETDDKGAVKHTVHREQGRWTYFPNKLAVTGDLNPDTRRLGLHKVLVYTWQGKAEADFAANIPANPVAPAGTTVSGITRVIGKPWLSYAFADVRGLRDPKLKLDGAQAAIEDGLGARDGGGIHARLAAPAPGTQLRLQTQLEFALGGTESLALVPLGKDNRFALNSSWPHPNFGGSFPPSSDGITDKGFKAEWRVSSVATNAQRQYQAGTIMPSVMVIGDDSVDSASGGDINAVQVTMKDPVNVYSQADRATKYGLLFVLLTFVGFFMFELIKQLRIHPIQYGLVGLALAIFFLLLVSLSEHIDFGLSYLAATVACIGLIVFYLSAVLRSMVRALGFGAMLVTLYGALYGLLISEDNALVLGAGLLFVILAAIMALTRKVDWYQIGGNAGPAVKRSVAAAPAGPAAPRDPSVPPAL
>NZ_CP011130.1|WP_057922098.1|3960028_3961471_-|two-component-system-sensor-histidine-kinase-CreC
MRIGLRIFLGYFLIVAVAALLLARVFVAEVKPGVRQAMEDTLVDTANILAELAADDFLAGRIDHGDFAKRVRALGERDVGAAIWGFRKRATTYRVYITDARGIVVFDSDGRDVGQDYSRWNDVYLTLRGRYGARSSPATPGNADETIMYVAAPIRDDARRVVGSLTVAKPNSAIAPFIARSQSVVMRWGFVLMGVALLIGVLVSWWLSRQIDLLRRYAHAVTAGARAPPPDAAGEFGELGRALETMRTRLEGKQYVEQYVHTLTHEMKSPLAAIRGSAELLESPPGDGTMPDADRARFAGSIRGQAERLAQMIDKLLALAAVEHRQRLEKPEPVALAAIAQEAAEQCAQRLHKTGAKLLLDLEPNLPPVLGDGFLLRQALINLIENAADFSPAQGEIVLRLRRDGEAQRVEVSDRGPGVPDYALGRVFERFYSLPRPAGGSRSSGLGLCFVAEVASLHGGGAALVNRDEGGAVASLVVPG
>NZ_CP011130.1|WP_036109243.1|3961481_3962153_-|two-component-system-response-regulator-CreB
MRILLVEDESAIADTVLYALRAEGFEATHCLTGGEALREAQRVAYDLAVLDIGLPDIGGFALCRELRRDRDLPVIFLTAQNAEADRILGLEIGADDYVTKPFSPRELATRVRVVLRRKGGANIPAESEAGFVHDGEGKRIRYRGQALDLTRYEYGLLAALLQRPGAVLSRAQLMDRVWGDALDSGDRTVDTHIKTLRAKLREIGPDSDPIRTHRGLGYSLELG
>NZ_CP011130.1|WP_046657281.1|3962342_3963203_+|23S-rRNA-(adenine(2030)-N(6))-methyltransferase-RlmJ
MNYRHAFHAGNHADVLKHIAVLALCDALTAKPAPLFALDTHAGRGLYPLDGNSAQRTGEAEGGIGRLLAEAPKQPAIGRYLAAVRACRAEHGPAAYPGSPWLLAHALREDDRIAACELQPEEAAQLKHHFDNDTRVAVHARDGYTGMKALLPPKLGATRFNRGLVLIDPPYEAQLEEFDTALGALRDALARWPQGIYVLWYPIKRRRSLQSFYRRAATLPAKSVMTAELLVRADDSPLRMNGSGLLLLNAPWQFDRTLDAVLPVLARTLGETADASAAITWLKQGD
>NZ_CP011130.1|WP_036109252.1|3963681_3963882_+|hypothetical-protein
MIRKKSTLLALCAFAFGIGMATTAIAACNNTCRLGCERAYSLCDPNTTDCELNYANCYRSCGCIIP
>NZ_CP011130.1|WP_036109254.1|3964146_3964371_+|hypothetical-protein
MTRPTKRSRTALLFVCTFVFTAGLSTTALAALCTPQAIVNCERIQRNCLSNGLPPDVCERAYLGCMGRAGCEVP
>NZ_CP011130.1|WP_057923605.1|3964432_3964924_-|GNAT-family-N-acetyltransferase
MGLLLSAPVARAYREDDHAACVALFQSNVPEYFAAVEIDDFLQTLQQVDRYWVIELAGEGIVACGGYDGINDQPGVAALCWGMVRRDLHRRGLGDFLVSERLRRIDADGDFNAVAIETTRFSCDFYARYGFEVIREQADGFAPGYDLVEMRRPVPWPRAARGG
>NZ_CP011130.1|WP_057922099.1|3964908_3965922_-|DUF1963-domain-containing-protein
MKTGKAVLVSVGIIAAVLAVAGGVGYFVYNKVESRSKQAAAQMKAEAERDDADRSAPQCGSHDDDERAKAVLAPIEPALQNTQRPVARIELETMKADDVAVSKVGGRAYWAAGRDYPRDPQGQPLFLLAQIQLGELPKMPGYPERGMLQFFISGDDFYGAAIDAAHGPKRMDALAEPNGFRVVYWADASAPAIVPPAATAGLDALPFDPAKPRRIRFSADHETMGIHDVGLAKVLGTDIDALAERYISANVDDRVAAEDLSDEVSDYLDRSGHKLGGYPDFTQDDPRGADDKRVLLFQLDSDDGLMWGDSGIANFFIDPADLARADFSRVSYHWDCY

Crispr_ID: NZ_CP011130_12

• CRISPR_ID: NZ_CP011130_12
• CRISPR_location: 3983381-3983473
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_12

Consensus_repeat	Method
CGAAAGTCCGGGAATGCAGTGAC	CRISPRCasFinder

spacers of NZ_CP011130_12

>12.1|3983404|47|NZ_CP011130|CRISPRCasFinder
CTGGAGTGATCATCTATGAGCCGAGGTGAAGTAGTTGCAGATCACGA

CRISPR arrays and Neighbor proteins around NZ_CP011130_12

CRISPR arrays

The CRISPR arrays of NZ_CP011130_12

>merge|NZ_CP011130|12|3983381-3983473|CRISPRCasFinder
CGAAAGTCCGGGAATGCAGTGACCTGGAGTGATCATCTATGAGCCGAGGTGAAGTAGTTGCAGATCACGACGAAAGTCCGGGAATGCAGTGAC

>NZ_CP011130|12|11|3983381-3983473|CRISPRCasFinder
CGAAAGTCCGGGAATGCAGTGAC	CTGGAGTGATCATCTATGAGCCGAGGTGAAGTAGTTGCAGATCACGA
CGAAAGTCCGGGAATGCAGTGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_148650449.1|3976462_3976942_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036109309.1|3993945_3994380_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_CP011130.1|WP_148650450.1|3986935_3987568_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922111.1|3988017_3989313_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_CP011130.1|WP_036109273.1|3975494_3976355_+|pirin-family-protein	unknown	unknown	gnl|CDD|224655
NZ_CP011130.1|WP_036109291.1|3983755_3984268_-|MOSC-domain-containing-protein	unknown	unknown	gnl|CDD|225167
NZ_CP011130.1|WP_057922109.1|3985870_3986722_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_082648588.1|3984308_3984872_+|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl|CDD|225567
NZ_CP011130.1|WP_057922105.1|3979756_3980344_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|226472
NZ_CP011130.1|WP_082648587.1|3974228_3974747_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|132718
NZ_CP011130.1|WP_057923606.1|3977163_3977874_+|aquaporin-Z	unknown	unknown	gnl|CDD|235453
NZ_CP011130.1|WP_057922103.1|3978080_3978326_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922113.1|3992246_3992885_-|EF-hand-domain-containing-protein	unknown	unknown	gnl|CDD|372618
NZ_CP011130.1|WP_057922106.1|3980402_3982802_-|bifunctional-23S-rRNA-(guanine(2069)-N(7))-methyltransferase-RlmK/23S-rRNA-(guanine(2445)-N(2))-methyltransferase-RlmL	unknown	unknown	gnl|CDD|236981
NZ_CP011130.1|WP_046659204.1|3982815_3983343_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|225496
NZ_CP011130.1|WP_057922102.1|3974848_3975262_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922104.1|3978583_3979444_-|pirin-family-protein	unknown	unknown	gnl|CDD|224655
NZ_CP011130.1|WP_057922112.1|3989452_3991747_-|DUF11-domain-containing-protein	unknown	unknown	gnl|CDD|307488
NZ_CP011130.1|WP_057922108.1|3984984_3985869_+|acyl-CoA-thioesterase-II	unknown	unknown	gnl|CDD|224857
NZ_CP011130.1|WP_036109306.1|3993077_3993821_+|arginyltransferase	unknown	unknown	gnl|CDD|234939

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_036109309.1|3993945_3994380_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.11736e-07
NZ_CP011130.1|WP_057922111.1|3988017_3989313_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	1.96853e-36
NZ_CP011130.1|WP_036109273.1|3975494_3976355_+|pirin-family-protein	gnl|CDD|224655	COG1741, COG1741, Pirin-related protein [General function prediction only].	1.118e-80
NZ_CP011130.1|WP_036109291.1|3983755_3984268_-|MOSC-domain-containing-protein	gnl|CDD|225167	COG2258, COG2258, Uncharacterized protein conserved in bacteria [Function unknown].	7.09355e-24
NZ_CP011130.1|WP_082648588.1|3984308_3984872_+|N-acetylmuramoyl-L-alanine-amidase	gnl|CDD|225567	COG3023, ampD, N-acetyl-anhydromuramyl-L-alanine amidase [Cell envelope biogenesis, outer membrane].	1.73705e-36
NZ_CP011130.1|WP_057922105.1|3979756_3980344_-|methyltransferase-domain-containing-protein	gnl|CDD|226472	COG3963, COG3963, Phospholipid N-methyltransferase [Lipid metabolism].	2.48356e-40
NZ_CP011130.1|WP_082648587.1|3974228_3974747_+|histidine-phosphatase-family-protein	gnl|CDD|132718	cd07067, HP_PGM_like, Histidine phosphatase domain found in phosphoglycerate mutases and related proteins, mostly phosphatases; contains a His residue which is phosphorylated during the reaction. Subgroup of the catalytic domain of a functionally diverse set of proteins, most of which are phosphatases. The conserved catalytic core of this domain contains a His residue which is phosphorylated in the reaction. This subgroup contains cofactor-dependent and cofactor-independent phosphoglycerate mutases (dPGM, and BPGM respectively), fructose-2,6-bisphosphatase (F26BP)ase, Sts-1, SixA, and related proteins. Functions include roles in metabolism, signaling, or regulation, for example, F26BPase affects glycolysis and gluconeogenesis through controlling the concentration of F26BP; BPGM controls the concentration of 2,3-BPG (the main allosteric effector of hemoglobin in human blood cells); human Sts-1 is a T-cell regulator; Escherichia coli Six A participates in the ArcB-dependent His-to-Asp phosphorelay signaling system. Deficiency and mutation in many of the human members result in disease, for example erythrocyte BPGM deficiency is a disease associated with a decrease in the concentration of 2,3-BPG.	1.05464e-16
NZ_CP011130.1|WP_057923606.1|3977163_3977874_+|aquaporin-Z	gnl|CDD|235453	PRK05420, PRK05420, aquaporin Z; Provisional.	1.83391e-124
NZ_CP011130.1|WP_057922113.1|3992246_3992885_-|EF-hand-domain-containing-protein	gnl|CDD|372618	pfam13499, EF-hand_7, EF-hand domain pair.	2.64074e-06
NZ_CP011130.1|WP_057922106.1|3980402_3982802_-|bifunctional-23S-rRNA-(guanine(2069)-N(7))-methyltransferase-RlmK/23S-rRNA-(guanine(2445)-N(2))-methyltransferase-RlmL	gnl|CDD|236981	PRK11783, rlmL, bifunctional 23S rRNA (guanine(2069)-N(7))-methyltransferase RlmK/23S rRNA (guanine(2445)-N(2))-methyltransferase RlmL.	0
NZ_CP011130.1|WP_046659204.1|3982815_3983343_-|alpha/beta-hydrolase	gnl|CDD|225496	COG2945, COG2945, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	2.70016e-07
NZ_CP011130.1|WP_057922104.1|3978583_3979444_-|pirin-family-protein	gnl|CDD|224655	COG1741, COG1741, Pirin-related protein [General function prediction only].	2.78973e-92
NZ_CP011130.1|WP_057922112.1|3989452_3991747_-|DUF11-domain-containing-protein	gnl|CDD|307488	pfam01345, DUF11, Domain of unknown function DUF11. A domain of unknown function found in multiple copies in several archaebacterial proteins. Conserved N-terminal lysine and C-terminal asparagine with central asp/glu suggests that many of these domain may contain an isopeptide bond.	0.00215425
NZ_CP011130.1|WP_057922108.1|3984984_3985869_+|acyl-CoA-thioesterase-II	gnl|CDD|224857	COG1946, TesB, Acyl-CoA thioesterase [Lipid metabolism].	2.11214e-130
NZ_CP011130.1|WP_036109306.1|3993077_3993821_+|arginyltransferase	gnl|CDD|234939	PRK01305, PRK01305, arginyl-tRNA-protein transferase; Provisional.	2.97004e-121

Protein sequences

>NZ_CP011130.1|WP_046659204.1|3982815_3983343_-|alpha/beta-hydrolase
MTPGHCILSHGFESGPDATKVTALAEAAQRLGWTHERPDYTDLDAKREVSELGDVYARIERLLGLARKAAQRGPVVLAGSSLGAYISGAVSMQVRPAALFLMAPPIAMGPAPVLQAADVPISIIHGWDDELIPAADVVAWAHPRRARLLLVDDSHRLTAHVQGSADAFARLLETL
>NZ_CP011130.1|WP_057922106.1|3980402_3982802_-|bifunctional-23S-rRNA-(guanine(2069)-N(7))-methyltransferase-RlmK/23S-rRNA-(guanine(2445)-N(2))-methyltransferase-RlmL
MSKFYASCGKGLEYLLADELIALGCQRATAATAGVNVEGELADAQRAVLWSRLASRVLWPITEFDCPDEHALYAGVAALDWPAHMESVHTLAVDAHVSGEAITHARYAAQRVKDGVVDVMRARTGSRPDVDTDQPDLRLNLVIRKGKAIVSIDLGGGSLHRRGWRQKQGEAPLKENLAAAVLLRGGWPKVYASGGGLFDPMCGSGTLLIEGALMAADVAPGLLRHGALPPTRWRGFDFAHWRVLCEQAREREAAGLAALRPVFAGSDIDPHAIRAARDNEIEAGLAGVIEWNVAAVESLQVAPARLQTTQLQATQFQATQFQATQFQAAQPEVRHPREGGDPETSESNLDKALDSRLRANDGLEEAISSEAGVGSGTNAHSDAQTPGLAVCNPPYDARLAADPALYRALGEALKRTVPSWRASLLCGDPALAQATTLRASKKYQIFNGAIECALIVCDPIARVGHAERKAQAEDAAPQPLSEGAQMVANRLRKNLRKLKNWRQREAVDCFRAYDADLPEYSAAIDVYTTDEAQPRTYLHVQEYAAPSDIPEADQRRRLNELLAAAREVFAVPRERLAIKTRARGKGGSKYGQFDQRGEFIVVREGAARLRVNPFDYLDTGLFLDHRPMRLRIAEEARGRRFLNLFGYTGAATVHAAVGSAHETTTVDLSATYLQWCSDNLRENGVTGSQHRLAQADAVQWLEADRGRYDLIFCDPPTFSNSARADDFDIQREHARLLRAAVARLADNGVLYFSNNFRRFRLDEEAIAQFARCVDISAQTIPPDFERDARIHRCWRLEPR
>NZ_CP011130.1|WP_057922105.1|3979756_3980344_-|methyltransferase-domain-containing-protein
MKSHRKPGTWTFFRQWLKNPLRVAAVAPSSAELAAAMISELPDDVNRVIELGGGTGAITRALLDAGIRDEDLLVLELNEELHAHLHLRFPQVPVVLGDARELPQLARDAGYLRTGPADAIVSGLGLLTMPHPLQRDILGAAFECLREDGVFVQFTYGPAAPVADPVARSLGLQVRRGDFVLRNVPPATVYVYTRV
>NZ_CP011130.1|WP_057922104.1|3978583_3979444_-|pirin-family-protein
MATATPTAYARVGRKLRGQPTSDGAGVRLTRVIGGPQLPDLDPFLLLDEFGTDKPEDYRAGFPEHPHRGFETVTYMLDGRMRHKDNHGNEGVLVPGSVQWMTAGRGLVHSEMPEQEAGRMRGFQLWVNLPAREKMTEPKYQEFAPDRIVQLQPADGVRIKLIAGRIGDVRGPIAQPATDPVYLDIALEAGASWEYELPEGHNAFAYVYEGGVQIGDGEEARAVDAQELAVLSGGNVLKLGDAKQGSRLIVIAGRPLREPVARYGPFVMNTKQEVMQAFVDFQEGKF
>NZ_CP011130.1|WP_057922103.1|3978080_3978326_-|hypothetical-protein
MATKLDPKQITLVATFVSAGVANGASGWMIVGGKLKKIPPRGIKQLQAVSQMLNAADAVGNARLAAQLQQTAIEVANEALH
>NZ_CP011130.1|WP_057923606.1|3977163_3977874_+|aquaporin-Z
MIKRLGAEFIGTFWLVLGGCGSAVLAANFGGAGNPLGIGLLGVALAFGLTVLTGAYAFGHISGGHFNPAVSFGLWAGGRFPAKDLFPYIVAQVLGGILAGFILLQIASGNGSFAIDPNAAGTFASNGYDLMSPGGYSLTAALLTEVVMTAMFLIIILGATHKNAPAGFAPIAIGLGLTLIHLISIPVTNTSVNPARSTGVALFAGAAAISQLWLFWVAPIVGGLLGGAVYRWLGKD
>NZ_CP011130.1|WP_148650449.1|3976462_3976942_+|hypothetical-protein
MKSWGKNQQAVPWLVLLFALCANAKAQDAAADDPGNCPALPASTGLRWEYRASADSDFCRALRADGSEAFGLYIASKSPFSPKRSDRAEASTIDGKAMHWYRGELAGKPDIQVRETLIEIGSGKIAHIWLQASSPDQLKEVIGQTEGLRFPSAQLSANK
>NZ_CP011130.1|WP_036109273.1|3975494_3976355_+|pirin-family-protein
MTTIIAPRIHDLGGFQVRRAVPSVQARSVGPFVFVDHMGPAAFEPGHGIDVRPHPHIGLATVTFLWAGAIGHRDTLGSVQDIHPGDVNWMTAGRGIAHSERTPDKPRADGHPLHGMQTWVALPRSFEETAPAFHHHPAATLPQLHRDGAWLRVVAGRGFGQESPVRVFADTLYVAIDLDPDKELEIEDSHAERALYLLEGQAQLDGADVPEKHLIVLDPGSRPRLRAKTPVKAMLLGGEPLDGPRHLWWNFVSSSRERIEQAKQDWAEGRFGHIPGEHEFIPLPER
>NZ_CP011130.1|WP_057922102.1|3974848_3975262_+|hypothetical-protein
MKSALIASMLSCVFALTACAHAAPSDPADAKPNGGGDAARPGQPLSMQPGDEVTLPDHSRLRFVAVTADSRCKPGLQCIWAGDATLEFQWTGSDGSQTSVSLNTPAEPSKSAGAWTFELQALDFAEPPHATVQFQAK
>NZ_CP011130.1|WP_082648587.1|3974228_3974747_+|histidine-phosphatase-family-protein
MAPITRLSVLSLSVLLAACASAPPTPTPNSSFVIVRHAEKANDDPRDPNLSEAGRARAERLAAALKNQPVRAVYATAYRRTQQTGEPTARSHGLQLVTYDAKQPATDFAASLRREHTAGTVLVVAHSNTAPDIAAALCQCTVAPMAETEFDRRMRIDFDRDGHPRYTESRDQ
>NZ_CP011130.1|WP_036109291.1|3983755_3984268_-|MOSC-domain-containing-protein
MTLPPADSALGKLMATLPRPGRVEWIGVRPARAVRMQALDEVVAQAGAGLAGDRYKGGSGKRGVTLIQAEHLPVIAALSGHASLEPALLRRNIVISGLPLLALKDRRFRLGDALLEWTESCDPCSMMEAALGPGGFNAMRGHGGLCARILEGGTIRRGDALVPVIDAVAV
>NZ_CP011130.1|WP_082648588.1|3984308_3984872_+|N-acetylmuramoyl-L-alanine-amidase
MPPLNLTSAPLPYEARLTPRDPASIDLVVIHCTELPDLATAREYGERVLYDESGTGNSGHYYIDRDGSVLRYVSEDRIAHHVRGYNPRSIGIELVNIGRYPHWLDSRRQAMPEDYTPAQIEALIALLNDLTQRLPSLRLIAGHEDLDTTQVESSDDPSVLVQRKLDPGPWFPWPRVLAACGLERLPR
>NZ_CP011130.1|WP_057922108.1|3984984_3985869_+|acyl-CoA-thioesterase-II
MTSSPVSELIELLSLERLEDNLFRGQSRDIGTKYVFGGQVLGQALSAAQATLDTARAAHSLHAYFLKAGDIEAPIVYQADRTRDGGSFSVRRVTAIQHGQPIFFLAASFHEDQDGGEHQLSMPEVPKPEDIDPAPAVPAQVMATLPTKVQRWLSRQGPFEFRHVYPRDELNPPKRPPYQQVWFRLSEPVGDAPELHRALLAYASDFHLLGTATFPHGISYYQPNVQMASLDHALWFHRPFRADDWLLYSIDSPSAQGARGLARGQIFDRHGHLVASSAQEGLIRVMAAQAPAKG
>NZ_CP011130.1|WP_057922109.1|3985870_3986722_+|hypothetical-protein
MRQVFSSPRLENVEGVAQLLRDAGIEVRVTNDRSYKGNRRSSFSYSEQPKERPAVWVVQSSDQLRARDLLREAGLIDSTRAEEAHHAPFRFQSSIDQTRTPGQKRAFRIKIGLLLCIAVVLGLAMFHNLRNRPVAAPAVDPAMVALQTHKFDGSVAAIPAGLAAAVFKQQLAEADQPTQCLRVDRNDASRKLLTALARSNLRLLPASQCVEVPDEEKGSHALDGAPAELIQVHAFRPTSASTGTVEYSAYFSRSQAVYKTLEVKLVDGNWTVVKTVKTVRAMG
>NZ_CP011130.1|WP_148650450.1|3986935_3987568_-|hypothetical-protein
MIARSLLPLAVLSALAMAPLSVARANDDPIVSTAKTSYSTNHEGPLYTQLLERPDIVDSQQIVDTHLVVANNELDCTAAVLELITDGWGYPAEIQPPTDRCASSRGAINELPPVNLPAGTMPGLWISDIARKPEPGQTTPTAKGRVVSIHSAGNIDFMFHNQMSPNWQYDAQPEDKTPFGTRIRVTQTKGTLIVDGRIIGQRFVLNPFGK
>NZ_CP011130.1|WP_057922111.1|3988017_3989313_+|sigma-70-family-RNA-polymerase-sigma-factor
MNAEALHSLIDHDLPAASRGDTAAYSRIVGACQNSITAIALAMVRDVHASEDIAQEAFLNAWQNIRKLQNPSSFLPWLRQITRNLATDHLRTRQRLPRGSDDFDAAIAAAADPEPSAVERLIEAERAQVAAELISALPDESREVLLLYYREGQSSQQVAALLGLSDAAVRKRLSRARSSVRGELLDRFAVFAQASAPTVGFTTLVASALGVIAPAGTTTAAIAAGSIGSGLAGKFGVGGLGTAGTSGGVVGSVVVFVVERVLSPVSEAVTGAPLDTASIATRMATIASPTLGGVIGGFVGGLIATVLIARYMLGFAATPQERREIGRLITIMSVTSALLAVATLVTLELSHGWVVPLSVTLAVIVVSLWQWLVVVPRALASSMARIQRETGRDPKHSLVYRWVLGPQAMVWSSLVMLASVVYVLYRDGRFG
>NZ_CP011130.1|WP_057922112.1|3989452_3991747_-|DUF11-domain-containing-protein
MALRHLFNAQPIGFRGLPGWRRRLAVATLAIVATILAPAAQADRAFAPRYQNPAVNGDITGIGNINLHCGGNVALCAQAQSGGITVVNQDPAIAMVYVDVDSDATTFNSSSANLALPAGSTVLFAGLYWSGISLSIARNSVRLRTPGSAVYASLSADELLTNSAGAFGDAAYQGFDDVTALVQAAGNGTYTVANVQTTQRGLGSLGSTWAGWALVIAYRDPAQTATRNLNVYDGLLSASDAALPVDIAFSGFITPATGPVNTTLGLLGWDGDDTVDGAVGLQYGRNAATLNNVSNAANPVNNFWNSSITRNGANVGARVPNYFDTLGMDLDFTPPNVPLPNGANSALIRARGSIDEVLIFGMISSATDVSRPNLKDRLLKSSADLNGGSLLPGELLEFTIGSTNVGSDASVQTVLTDVIPANTTYEPGSLVIVSGANAGAHSDAAGDDQAEFDAGNNRVVFRLGTGATAASGGTVAPGESFSLRFRVRVNAGVAAGTVINNSASVAHRSATLGENLLDVSDADAATPGDQPTRNVVAALPRIVLNKTSLRGVDSFSFALTNTAQAAGNVTTATAGTPAQVDGDVNTAGLQAYTVVAAGTDVTIAETGAPAGYALTSAVCRNAGNTVVGALAGTVYTIPGASVVADEVLTCAFTNTRSQAALSIVKSDASATYTPGGSAVYIITVRNDGPDAVAGALVEDVLPNGATLAAAWSCAIGAGSGACNPASGGAAGGGAVNLSVDLDSGATATITVSVNFAAAPEAYVP
>NZ_CP011130.1|WP_057922113.1|3992246_3992885_-|EF-hand-domain-containing-protein
MTRSPLYVAAFAAALLAGAAIAAPQTDAAAPQRQRIKLDANNDGVITREEASKLPRLAENFDKLDKNHDGKLDASERPQRRGGREHGGRGGHGGHGGAAALDTDGDGRISQAEAAKSPRLGEKFAQIDRNHDGYIVRSELRSYFESERPKREAERAKRFDEKFAAADLNHDGKLSKIEVDEKMPRLAKSFAFLDEDRDGFLTKADLKPTPHR
>NZ_CP011130.1|WP_036109306.1|3993077_3993821_+|arginyltransferase
MGTQPQPDSDDLRLFHTGEHACGYWPERTARDLVLDPRDPRLREWYPHALGWGFRRSGDIVYRPHCSGCRACVAVRIPVDRFVPDRSQRRCLARNAAVEMRVRPAERDEEQLALYKRYLASRHAGGGMDGHGALEFDQFLIGSWSENRFLELREPAPRGHGKLLAVAVTDVVDNALSAVYTFYDPDLADRSLGTLAILRQIEWAKRERRGHLYLGYWIAGHPKMDYKRRFRPLEAFDGRDWRVFTHS
>NZ_CP011130.1|WP_036109309.1|3993945_3994380_+|hypothetical-protein
MKLNTLFLAAAITLSLAACNKPADKPADAPAADAAAAPAADPAATPAPDAAPAAPMDPAMPAAAPAAASVGVAECDDYLAKVSACLTDKVPEAQRAAFQTGLDQSRNAWAQAAATPQGKEALANACKMALDQSKAQYASFGCTL

Crispr_ID: NZ_CP011130_13

• CRISPR_ID: NZ_CP011130_13
• CRISPR_location: 4421644-4421742
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_13

Consensus_repeat	Method
CGGTCGCGGCTCACGCCGCTCCTACA	CRISPRCasFinder

spacers of NZ_CP011130_13

>13.1|4421670|47|NZ_CP011130|CRISPRCasFinder
AGGGGGAGATCGCGCGCGGCTGAAGATGCGGCGCGTGTGAGGTGTCG

CRISPR arrays and Neighbor proteins around NZ_CP011130_13

CRISPR arrays

The CRISPR arrays of NZ_CP011130_13

>merge|NZ_CP011130|13|4421644-4421742|CRISPRCasFinder
CGGTCGCGGCTCACGCCGCTCCTACAAGGGGGAGATCGCGCGCGGCTGAAGATGCGGCGCGTGTGAGGTGTCGCGGTCGCGGCTCGCGCCGCTCCTACA

>NZ_CP011130|13|12|4421644-4421742|CRISPRCasFinder
CGGTCGCGGCTCACGCCGCTCCTACA	AGGGGGAGATCGCGCGCGGCTGAAGATGCGGCGCGTGTGAGGTGTCG
CGGTCGCGGCTCGCGCCGCTCCTACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057922315.1|4418778_4420074_+|glutamyl-tRNA-reductase	unknown	unknown	gnl|CDD|234592
NZ_CP011130.1|WP_082648628.1|4415732_4416743_-|outer-membrane-lipoprotein-LolB	unknown	unknown	gnl|CDD|234578
NZ_CP011130.1|WP_036111823.1|4410980_4412072_-|redox-regulated-ATPase-YchF	unknown	unknown	gnl|CDD|236583
NZ_CP011130.1|WP_057922314.1|4412790_4413450_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc	unknown	unknown	gnl|CDD|235534
NZ_CP011130.1|WP_057922316.1|4422380_4424105_+|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|226428
NZ_CP011130.1|WP_057922317.1|4425081_4425852_+|polyphosphate-kinase-2	unknown	unknown	gnl|CDD|213852
NZ_CP011130.1|WP_046657641.1|4409200_4410391_-|elongation-factor-Tu	unknown	unknown	gnl|CDD|234596
NZ_CP011130.1|WP_057922320.1|4428552_4429650_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922321.1|4429812_4430082_-|acylphosphatase	unknown	unknown	gnl|CDD|184675
NZ_CP011130.1|WP_036111835.1|4413626_4414586_-|ribose-phosphate-diphosphokinase	unknown	unknown	gnl|CDD|179893
NZ_CP011130.1|WP_046659261.1|4414760_4415717_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	unknown	unknown	gnl|CDD|234731
NZ_CP011130.1|WP_036111847.1|4424180_4424699_+|molybdenum-cofactor-biosynthesis-protein-B	unknown	unknown	gnl|CDD|131715
NZ_CP011130.1|WP_057922313.1|4412149_4412731_-|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl|CDD|235457
NZ_CP011130.1|WP_148650736.1|4416772_4418500_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|274350
NZ_CP011130.1|WP_036111841.1|4421887_4422358_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP011130.1|WP_057923628.1|4424704_4425085_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_CP011130.1|WP_148650480.1|4427031_4427403_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036111838.1|4420143_4421226_+|peptide-chain-release-factor-1	unknown	unknown	gnl|CDD|234801
NZ_CP011130.1|WP_187313242.1|4427429_4428356_+|DUF2145-domain-containing-protein	unknown	unknown	gnl|CDD|370750
NZ_CP011130.1|WP_046657650.1|4426102_4426846_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|379188

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057922315.1|4418778_4420074_+|glutamyl-tRNA-reductase	gnl|CDD|234592	PRK00045, hemA, glutamyl-tRNA reductase; Reviewed.	0
NZ_CP011130.1|WP_082648628.1|4415732_4416743_-|outer-membrane-lipoprotein-LolB	gnl|CDD|234578	PRK00022, lolB, lipoprotein localization protein LolB.	5.95044e-51
NZ_CP011130.1|WP_036111823.1|4410980_4412072_-|redox-regulated-ATPase-YchF	gnl|CDD|236583	PRK09601, PRK09601, redox-regulated ATPase YchF.	0
NZ_CP011130.1|WP_057922314.1|4412790_4413450_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc	gnl|CDD|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	9.68229e-76
NZ_CP011130.1|WP_057922316.1|4422380_4424105_+|tetratricopeptide-repeat-protein	gnl|CDD|226428	COG3914, Spy, Predicted O-linked N-acetylglucosamine transferase, SPINDLY family [Posttranslational modification, protein turnover, chaperones].	1.11161e-105
NZ_CP011130.1|WP_057922317.1|4425081_4425852_+|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].	7.61919e-135
NZ_CP011130.1|WP_046657641.1|4409200_4410391_-|elongation-factor-Tu	gnl|CDD|234596	PRK00049, PRK00049, elongation factor Tu; Reviewed.	0
NZ_CP011130.1|WP_057922321.1|4429812_4430082_-|acylphosphatase	gnl|CDD|184675	PRK14426, PRK14426, acylphosphatase; Provisional.	4.38577e-27
NZ_CP011130.1|WP_036111835.1|4413626_4414586_-|ribose-phosphate-diphosphokinase	gnl|CDD|179893	PRK04923, PRK04923, ribose-phosphate diphosphokinase.	0
NZ_CP011130.1|WP_046659261.1|4414760_4415717_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	gnl|CDD|234731	PRK00343, ipk, 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; Provisional.	2.65093e-145
NZ_CP011130.1|WP_036111847.1|4424180_4424699_+|molybdenum-cofactor-biosynthesis-protein-B	gnl|CDD|131715	TIGR02667, Molybdenum_cofactor_biosynthesis_protein_B., molybdenum cofactor biosynthesis protein B, proteobacterial. This model represents the MoaB protein molybdopterin biosynthesis regions in Proteobacteria. This crystallized but incompletely characterized protein is thought to be involved in, though not required for, early steps in molybdopterin biosynthesis. It may bind a molybdopterin precursor. A distinctive conserved motif PCN near the C-terminus helps distinguish this clade from other homologs, including sets of proteins designated MogA. [Biosynthesis of cofactors, prosthetic groups, and carriers, Molybdopterin].	1.97724e-102
NZ_CP011130.1|WP_057922313.1|4412149_4412731_-|aminoacyl-tRNA-hydrolase	gnl|CDD|235457	PRK05426, PRK05426, peptidyl-tRNA hydrolase; Provisional.	5.42537e-95
NZ_CP011130.1|WP_148650736.1|4416772_4418500_-|tetratricopeptide-repeat-protein	gnl|CDD|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	8.03987e-17
NZ_CP011130.1|WP_036111841.1|4421887_4422358_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	9.59594e-11
NZ_CP011130.1|WP_057923628.1|4424704_4425085_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000278134
NZ_CP011130.1|WP_036111838.1|4420143_4421226_+|peptide-chain-release-factor-1	gnl|CDD|234801	PRK00591, prfA, peptide chain release factor 1; Validated.	0
NZ_CP011130.1|WP_187313242.1|4427429_4428356_+|DUF2145-domain-containing-protein	gnl|CDD|370750	pfam09916, DUF2145, Uncharacterized protein conserved in bacteria (DUF2145). This domain, found in various hypothetical prokaryotic proteins, has no known function.	9.31502e-64
NZ_CP011130.1|WP_046657650.1|4426102_4426846_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	4.82079e-05

Protein sequences

>NZ_CP011130.1|WP_036111838.1|4420143_4421226_+|peptide-chain-release-factor-1
MTPTLRRKLEALVERREELERLLGDPGVIGDNDRFRKLSREFAQLEPVAIALAEEARAKADLAAAEAMRNDPELRELADEEILAAQARLEQLDVELLAHLIPKDPRDDGDLYLEVRAGTGGDEAAIFAGDLFRMYARYAERQGWKVEIESSNPGEHGGYKEIIGRVEGRGAYSKLKFESGTHRVQRVPETESQGRIHTSAATVAIIAVEPEGEPIEINPADLKVDTFRSSGAGGQHVNKTESAIRITHIPSGVVVENQTERSQHANRDKALKRLQAMLSDAAAAKAAAAQAQDRRLQVGSGDRSQRIRTYNFPQGRITDHRVEGLTLYDLPNIVAGDLDGLIGRLIHEHQADELARLSAS
>NZ_CP011130.1|WP_057922315.1|4418778_4420074_+|glutamyl-tRNA-reductase
MSLFVLGINHQTAPVSLRERVAFSGDAVASALTALRALAPVREVALLSTCNRTELYAVAEDGGDALAQWLATHPDDAGDLHAYLYRHRDADAVRHLFRVATGLDSLVLGEPQILGQVKDAWASARAAGTLGSQLDRLFQQAFSTAKRARTDTRIGANPVSVASAAVRLAQESFARLDDSTVLLIGAGETVELAARHLVQAKAKRLLIANRTLAHAQDLATRHGGVALPLSELDRHLGEADIVLSATASREPVLRKPQVAAALATRKHRPMLLLDLAVPRDIAADVAELKDVFLYTVDDLERSIEDNRRGRREAATEAEAIVDLQVARFVETLAASTRTAPIKRLRDHGQAAREEVLAKARQQLQSGQDPAEVLNFLAHTLTNRLLHAPTIALREAALTGNPELARAADKMFPAVGFGIGDSGFEKADADEP
>NZ_CP011130.1|WP_148650736.1|4416772_4418500_-|tetratricopeptide-repeat-protein
MRRLPIALLSVVLAFASGAVAAAAAPIQPSAAALAAARAQMQARAAKDPTGASLESLLSGEFSLQAGKLNDAATAYLKAARAAGDLALAERATTIAIVAKQDTTASESLALWRKLGGKGPTLNAAEATLALRRGDERDALRQLNNLMSGDPDTGWRQALGVLTAGSKTPQQAGRMLEKIIDGGQMPPRNLMAWVAFGGLAQRLDQPKLTERIVEEVVKRFPGEPRVALLRVSQLREDGKTEQAQQLLSTLVPLADTDNNLRALIAEQYEGLNDFQNVAAVLARGPQDEQTYALRASYLARAEDKPTLTRLYDELRADAAKPDPARRLLLAQMAEFLERNEEALNWYQGVPGGSQRSIARLRSANVLHKLHRGDEAYASLRAIQSDASAEDETRRDAYILEASLRAEDKSDSGESDAFARGLAAFPDEPEILYARALSWERRDDVARAEADFRRILVAEPDSVAALNALGYTLADRTTRYQEALELIERARTAEPDNSAIIDSYGWVLYRLGRVQEAETELRRALTLQKDAEIASHLAEVLWESGRRDEARKYFEQARKIDPENRSLLRALKKYGL
>NZ_CP011130.1|WP_082648628.1|4415732_4416743_-|outer-membrane-lipoprotein-LolB
MRAALTRTAVIAMLMLALSACVGGAVKRPAGETVVPAADAAQREAARAQRVRAGSEWSLTGRIAVSNAGKGGSGRIEWTQRGERFEVALSAPVTRQSWRLAGGPGEARLEGLEGGPRSGDNAAALLLETTGWDIPVEALGNWLRGLPAEGGAAAKLTPGPDGRPLSIEQGGWTIAYQWPASGDLPSRLDARRASARVRLIVDEWQGGAAAAPVASRDKGWESLQSNVVKLRNELATLNLDDPAGDARADLAQGRARLIGMCGFSCLTPGLEGGDSEGVDGVHYLDGTSDVIEGDEHARLLEQATRYAIAYNQSLGAGLKANAASGATAAHAASASR
>NZ_CP011130.1|WP_046659261.1|4414760_4415717_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase
MAPTSQSDAGANAAPVDDHSDGRAWSLWPAPAKLNLFLRIVGRRADGYHLLQTVFRLLDWGDTIRLRPRDDGRVVRHGASVAGVAEHDDLTVRAALLLQKEANSGQGADILIEKRIPAGGGFGGGSSDAATVLVALDALWGTDLGVDRLAELGLRLGADVPVFVRGENAWAEGVGESLRPIELAPAWYVLVDPGVHAPTAALFQSAELTRDAAPATISDFVSGKPLGNAFEPVLRKRETAVEAAFAALSRIGSPRLTGSGSGCFVEFATRETAEAALLELPSGLRAWTAGGAGRSPLHAALETRFPQGRRQEAQGTRF
>NZ_CP011130.1|WP_036111835.1|4413626_4414586_-|ribose-phosphate-diphosphokinase
MQNDRNLLVFSGNANRPLAEAVCKELGIRIGKALVGRFSDGEVQVEIEENVRRQEVFVIQSTNAPTAENFMELLVLIDALKRASVASVTAVVPYFGYARQDRRPRSSRVPITAKVAAKMFSAVGADRVLTVDLHADQIQGFFDIPVDNVYASPLLLADIWRAHGTDNLIVVSPDVGGVVRARAIAKRLDDAELAIIDKRRPRANVATVMNIIGDVSGKTCVLVDDIVDTAGTLCAAAAALKAQGAQKVVAYCTHPVLSGAAIDNVTKSQLDELVVTDTIPLTAAARATGRIRQLSVAELLAETIRRIAFGESVSSLYVD
>NZ_CP011130.1|WP_057922314.1|4412790_4413450_-|50S-ribosomal-protein-L25/general-stress-protein-Ctc
MSEHIIKATGRNVEGKGASRRLRRAASIPAIIYGGKNPPQAIQLDHEKIWLASQHEWFYSSILSLELDGKAQDVLLRDMQRHPFKQIIMHLDFQRVDANQAIRVAVPLHFLNEDKSPAGKAADVVVTHELNEVEVSCLPKDLPEFIEIDLSALTVGDIVHLSELKLPKGVEIPELKLGKEHDVAVVIAKHGKEEVEEAIDAPEADVPAAKVAKKDEDKK
>NZ_CP011130.1|WP_057922313.1|4412149_4412731_-|aminoacyl-tRNA-hydrolase
MAGLRLIVGLGNPGSEYARTRHNAGFWFVDALNEKFGGRFGLESKLFGETAKIEISGRPVWLLKPATFMNLSGKSVTAALRYWKIEPEEALLAHDELDLSPGTARLKFDGGHGGQNGLRDTMQLLGHGKFHRLRVGIGHPGHKDKVTPWVLGRPGKDDEATILRAIDNAIDVMPLAVQGNFMDAMTQLHTSRD
>NZ_CP011130.1|WP_036111823.1|4410980_4412072_-|redox-regulated-ATPase-YchF
MGIKCGIVGLPNVGKSTLFNALTKAGIAAANFPFCTIEPNVGAVPVPDLRLNALAEIVKPQKLIPTAVEFVDIAGLVAGAASGQGLGNKFLAHIREVDAITHVVRCFENPDVIHVNNKVDPIADIDTIDTELALADLESVEKAYQRAERSAKTGDKEAAARKEVLGRVREGLNAGTAARALKLSDDDKAAVRDLFLLTLKPVMYVANVLEDGFENNPHLDAVRARAVTEGAQVVPVSAAIEEELSQLDDEDRDTFLADLGLAEPGLNRLIRAGYELLGLQTYFTAGVKEVRAWTVKAGSTAPQAAAVIHTDFEKGFIRAETIAYDDFIKYKGESGARDAGRLRLEGKEYRVQEGDVLHFRFNV
>NZ_CP011130.1|WP_046657641.1|4409200_4410391_-|elongation-factor-Tu
MAKGKFERTKPHVNVGTIGHVDHGKTTLTAALTKVGAERFGGEFKAYDAIDAAPEEKARGITISTAHVEYESASRHYAHVDCPGHADYVKNMITGAAQMDGAILVCSAADGPMPQTREHILLSRQVGVPYIVVFLNKADMVDDAELLELVEMEVRELLTKYDFPGDDTPIIHGSARLALEGDQSEIGVPSILRLVEALDTFIPQPERDVDKPFLMPVEDVFSISGRGTVVTGRIERGIIKVGDEIEIVGIRATQKTTVTGVEMFRKLLDQGQAGDNAGLLLRGTKRDDVERGQVLCKPGSIKPHTDFEAEVYVLSKDEGGRHTPFFKGYRPQFYFRTTDITGACELPEGVEMVMPGDNVKMVVTLINPVAMDEGLRFAIREGGRTVGAGVVAKIIK
>NZ_CP011130.1|WP_036111841.1|4421887_4422358_+|GNAT-family-N-acetyltransferase
MSLTVRRAGLDDLDLLAPLFDRYRHFYTQRFDEAVSRSFLGERLSRGDSVLLLAALDGDDGAGFTQLYPMFSSVRAARVWVLNDLFVEAHARRRGVAQALLDAAAAFARADGAARLELETNHDNLGAQALYDAAGWQRFDGTQRYHLPLQPPAVSA
>NZ_CP011130.1|WP_057922316.1|4422380_4424105_+|tetratricopeptide-repeat-protein
MNDPRTPLRQALQLNPGDAMAWVSLADYELDAGDARSGEAAARRALSLRPGHPEALARLGRAQWMLGQREQAVTSLRAAARSAPQHPGIAVWLAHALEDIGDGEGALAAYSHAHALAPRHAQFAAYLLAWRRRLCDWSDLDALARQVRDAVAHSEASVEPFAFLSEDTSAAEQRRCAGLRAAQIAGVVRPLPPAPAKDPAAPIRAGFLSNGFGAHPTGLLTVALFEALRRRGGLEVQLFALNGDDDSPIRRRLHEAVAVMHDVSRQPHDQVAATIRRAGIDVLFDLRGWGGGGAPEVLAMRPAPVQVNWLAYPGTSGAPWIDYVLADRYVLPEALAADFSETVAWLPRCFQPSDTRRELPLPPPRGDCGLPEDAVVFCCFNNSYKLNPHSMARALAVLRGVPGSVLWLMSGPGRADQRLREFAAHQGLAPERLVFMRKQPHADYLARLRHADLFLDTNPYNAHTTASDALWAGCPVLTCPGATFAARVAGSLNHHLGMDSMNMADDAAFIARAIALGNDREALAELRNQLAARRRDSGLFDMDGFAVDFAAMTIAMARRQRKGEAPSVLQGPSR
>NZ_CP011130.1|WP_036111847.1|4424180_4424699_+|molybdenum-cofactor-biosynthesis-protein-B
MTAERDFIPLNLCVLTVSDSRSLAEDTSGDYLIQSLTDAGHRLVERKLLPDDRYKLRAAVSQWIADDGVDGILVTGGTGFTGRDSTPEALLPLLDKEMPGFGELFRAISYDEIGTSTLQSRAFAGLANATFLFCLPGSTSACRTAWEKIVSAQLDARTRPCNLATLRPRLKE
>NZ_CP011130.1|WP_057923628.1|4424704_4425085_+|helix-turn-helix-transcriptional-regulator
MSLDTTLRLLTKASGLSVTDLATAIPRAGAATVSAWLRGDKLPGRDQVDALARAFGVPAGALLADLASTLDPARTQGEHDLLAAYRALSTKQQGALLEVATAMAGTKRGAAGKPAAKSTGSRKAKR
>NZ_CP011130.1|WP_057922317.1|4425081_4425852_+|polyphosphate-kinase-2
MSKLKRKDYEEQLEALQLELAAMARWVQHHGKRVVVLLEGRDTAGKGGAINALSEHLNPRQCHIVALSKPSERESGQWYFQRYVPHLPAAGEIALFDRSWYNRAGVESVMGFAKPEQVKAFLKQAPAFEKLLTDDGIVLFKYWLCCDQKEQEERFAERLNDPLKRWKLSPIDLEARKHYDDYTKAREVMLEATHSKHAPWTLVDFNDQRQGRLSLIRDLLSRLPETKLPETELEFPPLKGKPSKEKYGVLRPIGKG
>NZ_CP011130.1|WP_046657650.1|4426102_4426846_-|helix-turn-helix-transcriptional-regulator
MALSLELVDALKRFLRAQDLTYRDLAVRLKLSEAAVKRMFSRRAMSLQRLEEVCEVLDIGLAELSAESARGRAPMAALSEAQEQALVDEPALLLALFLTLNRWKQADVQAHFNFDNVQWTALLVRLDRLGIIELMPGNRGRPLTARNFRWRADGPMERYFRHRLLGDFFADPFDGEQDVLLLLSGALSIAGIRQLKQRLGEVAREFDALLARDASLSAQERVGVSLVLAQKPWLLQLFQPYRRSQGD
>NZ_CP011130.1|WP_148650480.1|4427031_4427403_+|hypothetical-protein
MPARAAGQSDAVSRQSEASLNASVEVPVAAAHALSQGARFSVTGVAASAQGVAVTVSAAGAGASFVVVLSAKAAKDLGLAVGALVVVSVVAAGWLISDAAGHAICFVPDAAARALIHSARVGA
>NZ_CP011130.1|WP_187313242.1|4427429_4428356_+|DUF2145-domain-containing-protein
MSAASIGAVRTALFSFLVRTFVTGRMPAAGRRLAITLGVAVVVSGLLPAQGRAGTRCENATISPQSAAAAAQTALTVAAALDQRDAPAALVARVGTDLSAQGLVYSHVGFVVRDHPAGRWTAVHLLNECGSDRSNLYTQGLVNFFADDLVNQDARIVWLRPEQAQRLADYLRALPRGALHQPHYNLIARPGSADYQNSTAWVVETLAASLLESAGATRLSNNRREAYRAAEHDGFRPDRIHIPYSKRVLGGLFSANVAFTDHPIGTRLAGDYPVVTVRSIIEYLERSGHVDAQREWRNGQVVTRLGAL
>NZ_CP011130.1|WP_057922320.1|4428552_4429650_-|hypothetical-protein
MLPPLDRSYPTQLDTCKPPVPPADPRAPDLRPVEADYGPNQFEIGVDGPDPALAVGGSHDQQEQQRDYMLALATRGFASYLTGHTPGTPRYPSDGDVRNILADLNTNPPIGEVGVDVTRAVYQSNIPNATAQEAYQHFVDNPEQVFGAGGMEIRPPAGRLEDGGRYMLETGGPPPTWLPVEIRLDPGANAITINTLDGHVLRGTQTFTFTDDCNGGAVLSQDAIFQGSTQMVGDIQQLASVSGGQHNAWENAHREIYGQFNGDQDYTGIGTSAVSPDLIKGWGEMLKTIAADPGNFVDVLVDSGGELANETIDHWGGWAGDFLDWTGIPGGGVVRDVTDTIGDGVSTVADVGGDLIELGLKAKFW
>NZ_CP011130.1|WP_057922321.1|4429812_4430082_-|acylphosphatase
MSAARFFVAGKVQGVWFRASTREQAVALDLRGYANNLRDGRVEVLAVGEEAAIERLAQWLRQGPPMARVDALLREAASESEAGDGFVCG

Crispr_ID: NZ_CP011130_14

• CRISPR_ID: NZ_CP011130_14
• CRISPR_location: 4525109-4525227
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_14

Consensus_repeat	Method
CCTGTAGGAGCGGCGCAAGCCGCGACCGCG	CRISPRCasFinder

spacers of NZ_CP011130_14

>14.1|4525139|59|NZ_CP011130|CRISPRCasFinder
AATCCACAGACACCCGCGCTTGTTTGATTCACCACGCGCGCCGCCGCCCACATCGCCTA

CRISPR arrays and Neighbor proteins around NZ_CP011130_14

CRISPR arrays

The CRISPR arrays of NZ_CP011130_14

>merge|NZ_CP011130|14|4525109-4525227|CRISPRCasFinder
CCTGTAGGAGCGGCGCAAGCCGCGACCGCGAATCCACAGACACCCGCGCTTGTTTGATTCACCACGCGCGCCGCCGCCCACATCGCCTACCTGTAGGAGCGGCGCAAGCCGCGACCGCG

>NZ_CP011130|14|13|4525109-4525227|CRISPRCasFinder
CCTGTAGGAGCGGCGCAAGCCGCGACCGCG	AATCCACAGACACCCGCGCTTGTTTGATTCACCACGCGCGCCGCCGCCCACATCGCCTA
CCTGTAGGAGCGGCGCAAGCCGCGACCGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_046657704.1|4531101_4531656_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	unknown	unknown	gnl|CDD|376665
NZ_CP011130.1|WP_148650487.1|4527056_4527422_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922371.1|4531658_4532570_+|histone-deacetylase-family-protein	unknown	unknown	gnl|CDD|212541
NZ_CP011130.1|WP_057922365.1|4525387_4526731_+|MFS-transporter	unknown	unknown	gnl|CDD|340927
NZ_CP011130.1|WP_057922370.1|4530491_4531085_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_082648645.1|4533613_4534111_-|peptide-methionine-(R)-S-oxide-reductase-MsrB	unknown	unknown	gnl|CDD|234692
NZ_CP011130.1|WP_057922363.1|4520399_4522148_+|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	unknown	unknown	gnl|CDD|235424
NZ_CP011130.1|WP_057922361.1|4514582_4515155_+|DJ-1/PfpI-family-protein	unknown	unknown	gnl|CDD|153234
NZ_CP011130.1|WP_057922360.1|4513342_4514299_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|182999
NZ_CP011130.1|WP_057922362.1|4516272_4517922_+|hypothetical-protein	unknown	unknown	gnl|CDD|371971
NZ_CP011130.1|WP_148650737.1|4528780_4530034_-|2-octaprenyl-6-methoxyphenyl-hydroxylase	unknown	unknown	gnl|CDD|235584
NZ_CP011130.1|WP_057922366.1|4526749_4527055_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036115583.1|4522857_4523928_+|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	unknown	unknown	gnl|CDD|236971
NZ_CP011130.1|WP_148650488.1|4532893_4533328_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922364.1|4524128_4524875_+|hypothetical-protein	unknown	unknown	gnl|CDD|235334
NZ_CP011130.1|WP_057923631.1|4515382_4516033_-|peptide-methionine-(S)-S-oxide-reductase-MsrA	unknown	unknown	gnl|CDD|234604
NZ_CP011130.1|WP_057922368.1|4527584_4528784_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|181552
NZ_CP011130.1|WP_036115574.1|4518717_4519653_-|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP011130.1|WP_036115576.1|4519902_4520184_-|DUF2007-domain-containing-protein	unknown	unknown	gnl|CDD|378182
NZ_CP011130.1|WP_036115615.1|4522165_4522720_+|nucleoside-deaminase	unknown	unknown	gnl|CDD|238612

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_046657704.1|4531101_4531656_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	gnl|CDD|376665	pfam01923, Cob_adeno_trans, Cobalamin adenosyltransferase. Cobalamin adenosyltransferase This family contains the gene products of PduO and EutT which are both cobalamin adenosyltransferases. PduO is a protein with ATP:cob(I)alamin adenosyltransferase activity. The main role of this protein is the conversion of inactive cobalamins to AdoCbl for 1,2-propanediol degradation.The EutT enzyme appears to be an adenosyl transferase, converting CNB12 to AdoB12.	1.90772e-82
NZ_CP011130.1|WP_057922371.1|4531658_4532570_+|histone-deacetylase-family-protein	gnl|CDD|212541	cd11599, HDAC_classII_2, Histone deacetylases and histone-like deacetylases, classII. This subfamily includes eukaryotic as well as bacterial Class II histone deacetylase (HDAC) and related proteins. Deacetylases of class II are Zn-dependent enzymes that catalyze hydrolysis of N(6)-acetyl-lysine residues of histones (EC 3.5.1.98) and possibly other proteins to yield deacetylated histones/other proteins. In D. discoideum, where four homologs (HdaA, HdaB, HdaC, HdaD) have been identified, HDAC activity is important for regulating the timing of gene expression during development. Also, inhibition of HDAC activity by trichostatin A is shown to cause hyperacetylation of the histone and a delay in cell aggregation and differentiation.	1.6625e-157
NZ_CP011130.1|WP_057922365.1|4525387_4526731_+|MFS-transporter	gnl|CDD|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.55055e-79
NZ_CP011130.1|WP_082648645.1|4533613_4534111_-|peptide-methionine-(R)-S-oxide-reductase-MsrB	gnl|CDD|234692	PRK00222, PRK00222, peptide-methionine (R)-S-oxide reductase MsrB.	8.96179e-88
NZ_CP011130.1|WP_057922363.1|4520399_4522148_+|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	gnl|CDD|235424	PRK05347, PRK05347, glutaminyl-tRNA synthetase; Provisional.	0
NZ_CP011130.1|WP_057922361.1|4514582_4515155_+|DJ-1/PfpI-family-protein	gnl|CDD|153234	cd03140, GATase1_PfpI_3, Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. PfpI is an ATP-independent intracellular proteases which may hydrolyze small peptides to provide a nutritional source. Only Cys of the catalytic triad typical of GATase1 domains is conserved in this group. This Cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow.	2.52204e-54
NZ_CP011130.1|WP_057922360.1|4513342_4514299_+|LysR-family-transcriptional-regulator	gnl|CDD|182999	PRK11151, PRK11151, DNA-binding transcriptional regulator OxyR; Provisional.	1.63346e-106
NZ_CP011130.1|WP_057922362.1|4516272_4517922_+|hypothetical-protein	gnl|CDD|371971	pfam12222, PNGaseA, Peptide N-acetyl-beta-D-glucosaminyl asparaginase amidase A. This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 558 and 775 amino acids in length. There is a conserved TGG sequence motif. PNGase A is a protein which cleaves glycopeptides.	3.66156e-65
NZ_CP011130.1|WP_148650737.1|4528780_4530034_-|2-octaprenyl-6-methoxyphenyl-hydroxylase	gnl|CDD|235584	PRK05732, PRK05732, 2-octaprenyl-6-methoxyphenyl hydroxylase; Validated.	6.84862e-155
NZ_CP011130.1|WP_036115583.1|4522857_4523928_+|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM	gnl|CDD|236971	PRK11760, PRK11760, putative 23S rRNA C2498 ribose 2'-O-ribose methyltransferase; Provisional.	0
NZ_CP011130.1|WP_057922364.1|4524128_4524875_+|hypothetical-protein	gnl|CDD|235334	PRK05035, PRK05035, electron transport complex protein RnfC; Provisional.	2.81919e-06
NZ_CP011130.1|WP_057923631.1|4515382_4516033_-|peptide-methionine-(S)-S-oxide-reductase-MsrA	gnl|CDD|234604	PRK00058, PRK00058, peptide-methionine (S)-S-oxide reductase MsrA.	6.71219e-145
NZ_CP011130.1|WP_057922368.1|4527584_4528784_-|FAD-dependent-oxidoreductase	gnl|CDD|181552	PRK08773, PRK08773, UbiH/UbiF family hydroxylase.	0
NZ_CP011130.1|WP_036115574.1|4518717_4519653_-|DMT-family-transporter	gnl|CDD|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	1.5049e-08
NZ_CP011130.1|WP_036115576.1|4519902_4520184_-|DUF2007-domain-containing-protein	gnl|CDD|378182	pfam09413, DUF2007, Putative prokaryotic signal transducing protein. This is a family of putative prokaryotic signal transducing proteins of Pii-type.	2.47043e-12
NZ_CP011130.1|WP_036115615.1|4522165_4522720_+|nucleoside-deaminase	gnl|CDD|238612	cd01285, nucleoside_deaminase, Nucleoside deaminases include adenosine, guanine and cytosine deaminases. These enzymes are Zn dependent and catalyze the deamination of nucleosides. The zinc ion in the active site plays a central role in the proposed catalytic mechanism, activating a water molecule to form a hydroxide ion that performs a nucleophilic attack on the substrate. The functional enzyme is a homodimer. Cytosine deaminase catalyzes the deamination of cytosine to uracil and ammonia and is a member of the pyrimidine salvage pathway. Cytosine deaminase is found in bacteria and fungi but is not present in mammals; for this reason, the enzyme is currently of interest for antimicrobial drug design and gene therapy applications against tumors. Some members of this family are tRNA-specific adenosine deaminases that generate inosine at the first position of their anticodon (position 34) of specific tRNAs; this modification is thought to enlarge the codon recognition capacity during protein synthesis. Other members of the family are guanine deaminases which deaminate guanine to xanthine as part of the utilization of guanine as a nitrogen source.	4.05502e-28

Protein sequences

>NZ_CP011130.1|WP_057922364.1|4524128_4524875_+|hypothetical-protein
MQQHANRSKHSFSKHAFSKRSLLALALLTAFAAGSAQAQVPSKVQSKHDAIEKAEMAAAEARAARQDAQTAQAAAQAAAATRDEGALTARGALTAEATAYDAKQSALDAQDAAIKARRAAEAARSAQASAVSGNNPTGAAIEARAAMNEAMTASSIATDATTTAQAAASATADAVQQTGATTTQTMPRAMDSTIEPRIDFSALDTNRDGSISRVEASLSPALTADFAIADRDADGRLSQRELAGWAPR
>NZ_CP011130.1|WP_036115583.1|4522857_4523928_+|23S-rRNA-(cytidine(2498)-2'-O)-methyltransferase-RlmM
MTESALLCWCRAGFEPELAAELNERAAIAGHPGYARTQRNSGYVEFIVEDANALSRALPWSQLIFARQKLVRIADLSDLNPADRITPMLAALDALGGSGLNVSMFGELLVEHPDSDEGKQLSGLARSFGNALRPALRKAGWLSKTDDARRPRLHVAFVAGDHAMLALSDPLDSSPWPLGIPRLRMHPDAPSRSALKLEEALLTFLDADERQRRVRDNMQAADLGAAPGGWTWVLMRNGMMVTSVDNGPLKQELIDSGRVDHLRADGFTWQPRRTLDWMVCDMVESPARVAERMATWFRENWCRQAIFNLKLPMKKRWEETRICLEAFEHQAHRPLIVRARQLYHDREEITVFATPK
>NZ_CP011130.1|WP_036115615.1|4522165_4522720_+|nucleoside-deaminase
MLTASVTLALPSWIDEVVDRKRAYLGDDDKVALAIELSRHNIELGTGGPFGAAVFDGNGLVVGVGVNRVVPQNCSVAHAEMMAFMCAQAAVSAFRLNEIGPMTLATSAQPCCMCYGASFWAGINNLLIGARSEDVMRLTEFDEGPLPADWVGELERRGIAVRRDLHRDAACDVLRRYGESGVSY
>NZ_CP011130.1|WP_057922363.1|4520399_4522148_+|glutamine--tRNA-ligase/YqeY-domain-fusion-protein
MAPEIPTDTAATSAVKQDFVRQIVRDDLASGKHQAIRTRFPPEPNGYLHIGHAKAIALDFGIAGEFGGRCNLRFDDTNPAKEDPEYVAAIQEDVRWLGFDWAELRHASDYFEVFYLAGEKLIRQGDAFVCDLSAEEVRAYRGSLNEPGRNSPYRDRSVEENLDLFRRMRAGEFADGARTLRAKIDMASGNINLRDPALYRIKKVAHQNTGDAWPIYPMYDFAHSLSDSCEGITHSLCTLEFEDHRPLYDWCVAKVDLPNSPELLAPLLAKGYPNEAAIPRQIEFSRANLNYTVMSKRKLMVLVQEGLVDGWDDPRMPTLQGIRRRGYTPASLRLFADRLGVSKQNSTIDYSVLEGCLREDLDAAAARRMAVIDPLKLVITNLDDAHEESLQFSNHPKDESFGSRQVPFSNQLWIEREDFEEVPPKGFKRLIPGGEVRLRGAGILRCDEVIKNDAGEIVELRGTLDPESRPGMAGADRKIKGTIHWVSARHAVEAEVRLYDRLFDVSAPDDDSDGKTYQDHLNPNSRRAVTGYVEPSAAQVAPEQALQFERVGYFVADRYDHSPGRPVFNRSVTLRDTWASKE
>NZ_CP011130.1|WP_036115576.1|4519902_4520184_-|DUF2007-domain-containing-protein
MKVVYEAAHLIDAHLVRHALEDAGIPVFLRGEALLGGIGELPVFGAVQVCVPEAAWPRAREVVEALSLGDPPPDVADEPDPVGGLPPTGWLPA
>NZ_CP011130.1|WP_036115574.1|4518717_4519653_-|DMT-family-transporter
MNAAAHAPSSRTPLLQMLLGASVISSSAVFVKWVEIGPAASAFWRMALAAVILLVLLGQPWRRGRMRHWRPDGRVLGLVMLGAAFLALDLWLWHRSILYVGVGLSTLLANFQVFVLAGVGALFLGERAGWRLWVGLIMGLIGLGLLLAPGWESMDARFRLGVAFGLAAALAYGGFLLAFRAAQARRGPTPNEALQWWLCLGCAVMLGVSVPFGGETLLPASAHDWLILTAYAAIAQVLGWLVIGRAMPKLPAGVVGLCLLLQPLLAYVWDVLLFHKSLGAIELVGIGLSLAGIFLGLARGDQPLFSARQDA
>NZ_CP011130.1|WP_057922362.1|4516272_4517922_+|hypothetical-protein
MNPHLLRVGLISTGLLSAALAFAAPAHAADEFGSDWDDPRTADPTVARPDTRSCTVEILDTAFADFDWHPGAIAPPAACPGPWSKVVLEMDGQVKGVQYDRLGYLQIAGMTVLSTSTPEPSRDGIGWHVEKDISAYASLLKSPQAVRMYLGNVVNQTYTGVIYIQARVVFYTADRRHRALDSADVVAPLANERRDGADLIGDYTLPANATRWLGEVYATGSGGGCEEFWYFTAPPEANYSCPAQHGAYREVQVLIDGRVAGIAMPYPHIYTGGWSNPFLWYVIPAPRAFNIEPIRYDLTPFIGLVNDGRAHEVRFRVANLPDGASGWTLQPNLQAWTDARRGATGGRLLSYELTPLAAKSVYTALPDGTFKLDTRGGHRLRASGYVDTSKGREFTSIDRIVGNENLHTWGAEENPDGVKGEWNDTQTVTRIGRGLPTVAVQSQRFGLDGSISVVPSGDYQRIVTTMKIFDEANALQTPGLGQPLIAQATRNSFEGEAGWNYGVPRPERHATGHSTQRHRSVGTQGCYDHEIAQENGFIQLDRYRCGGAR
>NZ_CP011130.1|WP_057923631.1|4515382_4516033_-|peptide-methionine-(S)-S-oxide-reductase-MsrA
MPGIGAFKQRLPQREDALPGRAQELPLHNRHFVNGQPLRDAFAGLARVQFGMGCFWGAERKFWTVPGVVTTAVGYSGGYTPNATYREVCSGQTGHTEAVLVVYDPKQVAFEDLLKVFWESHDPTQGMRQGNDAGTQYRSAIYCEDESQYQAALASRDAFQVKLREAGFGDITTEIPEPPAPVFYYAEDEHQQYLAKNPMGYCGLGGTGVSCPIGVV
>NZ_CP011130.1|WP_057922361.1|4514582_4515155_+|DJ-1/PfpI-family-protein
MSKTIAFVMIDRPADWEYGPLAGAAHAWFGVDVVSASIDGTPLTTMGGLTLQPHIRLAELDPLAADLWVLPGSALWDEAPAPEAIVAALRLRAAAGRPIAGICGGTRGLAAAGLLDERAHTSNEPGYLDEVVGYRGKAHYRDAACVSDGGVVTAPGSSPISFAEACLRIVVPEQAEGIAQMRAMFARDFG
>NZ_CP011130.1|WP_057922360.1|4513342_4514299_+|LysR-family-transcriptional-regulator
MNLRDLKYLVALSDHKHFGRAAAASFVSQPTLSTQIKKLEEELGVSLVERAPRRVMLTPVGRDIAERARKVIADVEQMSEIARRSQDPEAGSVRLGLFPTLGPYLLPHVVPGLRKRFPRLELLLVEEKTDQILARLRDGRLDAGLLALPIHDDQLHVEPLFDEPFLLAVPQQHPMAGRDSLDLHDLDDQHLLLLEEGHCLREQALDVCRLAGADERDGFRATSLETLRQMVASGVGITLLPMLSVQPPVPPSPDIHLLRFNGESPHRQIGMLWRRSSAMSEFLMQLALELRKLPASLLQAPRPVGEKRRSARGRIEGT
>NZ_CP011130.1|WP_057922365.1|4525387_4526731_+|MFS-transporter
MPASPVPTGSASIESDSLERAPARRLDRKDARTLMLAALGGALEFYDFVIFVFLTETLRHLFFPPDMPGWLSTLQIYGIFAAGYLVRPIGGIVMAHFGDRSGRKRMFTLSVLLMALPTLCIGLLPVYAQIGVAAPLLLLSLRIVQGIAIGGEVPGAWTFVAEHVPRGRVGFACASLSAGLTAGILIGSLISTAINTWFTPEQVLGGVWRAPFVLGGVFGFLAVYLRRWLSETPVFAAMRESRQLVRELPLKRVLRDHLGGVVLSMLVTWLLTAAIVVIILMTPTIVQQQFGIAPARAFFGNSLAAFCLTLSAIGGGLLVDWLGRGRALLIGSLGVLVSSFALYYDLNHGAEHFLALYALAGVFVGVVGVIPAVMVAAFPAPVRFSGLSFSYNVAYAVFGAATPPLIGGYLAPHLGGMAPAYYVMGVAVVGMAVAVYLLNTKRRFHED
>NZ_CP011130.1|WP_057922366.1|4526749_4527055_-|hypothetical-protein
MRRLSQRLSLAAVAAWPLLAAATLRCPPEYGEKSAGFWALGFCVLGVFVLLGVAIPIAAIRITRGRRVARRVAWTLAACVPMLGLWLAGLLVFVEFFTLRC
>NZ_CP011130.1|WP_148650487.1|4527056_4527422_-|hypothetical-protein
MENTHMDEAIPASNRHTRSLCTRGFARLGIAISAAWPMLAAATTQCPPGSTDKNGLFWAVAFTVLGLFLLLGLVAPAAAIRFTRARKTVARVLWTLAACAPMLAVWLLGLFVFGRVFIMSC
>NZ_CP011130.1|WP_057922368.1|4527584_4528784_-|FAD-dependent-oxidoreductase
MSRREVLDIVVVGAGVVGAAAALAFARDGFEVALVEAREPAAWSPEDPDLRVYAFAPDNAAFVDDLGVWGAVQAARLQPYRAMRVWDAAGGGELHFDADAFGRRELGWIVEHGVLVDRLWSALPGAGVRLHCPDAVEALEHDASDGVGVALASGRRLRARLVVAADGAQSRLRELAGIEAPAHDYGQRGLVAYVDSELSHEATCWQRFLPGGPLAFLPAVGAPGARDRRSSIVWTLPNAEAERLLALDDAAFLDELERAFAGRLGALTGVSKRAAFPLRRQLAERYVAGRVVIAGDAAHVVHPLAGQGVNLGLRDISGLRGVLAQARKRGLDIGSPARLQRWARERRSENALAAYGFDGLNKLFSNDDFAATMLRGPLLGLAGKLPPLTHYFWRRAAGV
>NZ_CP011130.1|WP_148650737.1|4528780_4530034_-|2-octaprenyl-6-methoxyphenyl-hydroxylase
MHASHDVLIVGGGLVGASLAIALDRLGLDVGLIEAAPPGALPAVFDERNLSFAEATLNALGALGVLAKLRAPTGSIQRIHISRRGDFGRTVLDAQRYGREEFGRIVVARDFGEALEARLAELPRLHRYRPVRFVGLADDADPGWRAIRVADGAGERILRARLVVAADGTRSGVRDALGIAADEYDYGQTLFVTRLRSERAPDGTAYERLGDDGPTALLPRGDRHYGFIHGVANAQADAVAALDEAGFLARAQDAFGWRAGRFVSCGARSLYPAIRVLAARTIAPRAVLVGNAAQTIHPIGAQGFNLGLRDAMTLAELIEHDLAAGAEKADCGSADLLERYAQRRKPDRDRTVEFSDGIARLASNETALMRPLRSLGLFALDRMPTAQSLLVGGAMGYRGDVPALCRGDEPMLRGGRA
>NZ_CP011130.1|WP_057922370.1|4530491_4531085_+|hypothetical-protein
MKPNTQRTLILALLAVLMIGTRVNHWTPIPDASWAVFFIGGFYLRNWTRWAFPLLMVLAVAIDYAVITGQGMSFWQHYCVSAAYWFLVPAYFAMWAGGLWVARNYSRSWRTLGLTAVALLASVAVCQLLSQGSFYWLSDSVANKSVAGWAANYFEWLLPYLRTTATYVGIATLVQAIAAGASKTDALPGRSDDARKR
>NZ_CP011130.1|WP_046657704.1|4531101_4531656_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase
MGNRLSKIYTRTGDDGSTGLGDGSRTGKDSARVDAYGTVDEANSTIGLVLASELPQLVRDQLVAIQHQMFDLGAELCIPGHAAIFDADIDRLEQWLDGHNEDLPPLKEFILPAGGEAAARCHIARTVVRRAERETVALSRLESIRPEAVRYLNRLSDLLFVLARVLARASGHGEVTWNHERRKG
>NZ_CP011130.1|WP_057922371.1|4531658_4532570_+|histone-deacetylase-family-protein
MRIYTHPACTRHDPGPGHAERPLRLVAVTEALREAFPDLDWREAPAASRGQLLRAHTDELLALVLDTALDGPMHLDPDTVLAPGSAEAALRAAGAGVAAVDAVLKGETQRVFCAVRPPGHHATFEVAMGFCLFNNIAVAAAHACEKHGLSRVAVIDFDVHHGNGTQAIFDSDPRVMYVSSHQMPLYPDTGSVHERGVGNIVNAPLAPGTGSEGFRRVWRERLLPTIDSFRPQLVLISAGFDAHKRDPLAQVELEGEDFAWITRELVAIADRHALGRVVSMLEGGYDLAALRESAVAHVGALMA
>NZ_CP011130.1|WP_148650488.1|4532893_4533328_+|hypothetical-protein
MRALDSKQERLFLWLLSFVALDKRKLPAALAAEAFDPASSFESFESFESFESFESSRAYEAKGKINSFRPQAAELLSFVKSDKRKVTKEKRFLVNQGPARSLQTRARATRDILSRWRAAHIHVRRPSGVLLFSRVTRVAALAAD
>NZ_CP011130.1|WP_082648645.1|4533613_4534111_-|peptide-methionine-(R)-S-oxide-reductase-MsrB
MSQHPDPNPHPAAPAATQPSAEPQAIAPPAVAKSEAEWREQLSPEQYAVCRCSATERAFTGKFWNHKEAGTYTCVACGEPLFSSDAKYDSGSGWPSYWQPLAPEAVTEHADESHGMRRIEVKCARCDSHLGHLFPDGPRPTGLRYCINSASLGFEGAGEGKAPGG

Crispr_ID: NZ_CP011130_15

• CRISPR_ID: NZ_CP011130_15
• CRISPR_location: 4631614-4631780
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_15

Consensus_repeat	Method
GACGCGGTCGCGGCTCGCGCCGCTCCTACAGGGGGCGGCCGCGGCTTCGTTTCGC	CRISPRCasFinder

spacers of NZ_CP011130_15

>15.1|4631669|57|NZ_CP011130|CRISPRCasFinder
GCTGTAGGAGCGCCGCTAGTCGCGACCGCGACCTCACAGCCACGACGCAAGCGCGTA

CRISPR arrays and Neighbor proteins around NZ_CP011130_15

CRISPR arrays

The CRISPR arrays of NZ_CP011130_15

>merge|NZ_CP011130|15|4631614-4631780|CRISPRCasFinder
GACGCGGTCGCGGCTCGCGCCGCTCCTACAGGGGGCGGCCGCGGCTTCGTTTCGCGCTGTAGGAGCGCCGCTAGTCGCGACCGCGACCTCACAGCCACGACGCAAGCGCGTAGACGCGGTCGCGGCTCACGCCGCTCCTACAGGGGGCGGCCGCGGCTTCGTTTCGC

>NZ_CP011130|15|14|4631614-4631780|CRISPRCasFinder
GACGCGGTCGCGGCTCGCGCCGCTCCTACAGGGGGCGGCCGCGGCTTCGTTTCGC	GCTGTAGGAGCGCCGCTAGTCGCGACCGCGACCTCACAGCCACGACGCAAGCGCGTA
GACGCGGTCGCGGCTCACGCCGCTCCTACAGGGGGCGGCCGCGGCTTCGTTTCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057922404.1|4635968_4636847_-|PhzF-family-phenazine-biosynthesis-protein	unknown	unknown	gnl|CDD|223461
NZ_CP011130.1|WP_187313252.1|4637187_4637358_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036112801.1|4605384_4605660_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036107789.1|4628787_4629375_+|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl|CDD|223854
NZ_CP011130.1|WP_057922406.1|4639760_4641149_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP011130.1|WP_082648909.1|4641175_4642273_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224753
NZ_CP011130.1|WP_057922397.1|4605656_4619555_-|hypothetical-protein	unknown	unknown	gnl|CDD|225750
NZ_CP011130.1|WP_057923640.1|4620069_4622217_-|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase	unknown	unknown	gnl|CDD|223394
NZ_CP011130.1|WP_057922399.1|4622919_4623405_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922400.1|4624350_4628550_-|DUF3418-domain-containing-protein	unknown	unknown	gnl|CDD|273900
NZ_CP011130.1|WP_187313251.1|4635110_4635356_+|hypothetical-protein	unknown	unknown	gnl|CDD|370723
NZ_CP011130.1|WP_082648653.1|4633906_4635031_-|collagen-like-triple-helix-repeat-containing-protein	unknown	unknown	gnl|CDD|374271
NZ_CP011130.1|WP_057922405.1|4637579_4638563_-|glycoside-hydrolase-family-6-protein	unknown	unknown	gnl|CDD|376532
NZ_CP011130.1|WP_057922401.1|4629688_4631506_+|DNA-helicase-RecQ	unknown	unknown	gnl|CDD|273594
NZ_CP011130.1|WP_057922408.1|4642368_4642731_+|hypothetical-protein	unknown	unknown	gnl|CDD|178882
NZ_CP011130.1|WP_046657740.1|4631927_4633640_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	unknown	unknown	gnl|CDD|225387
NZ_CP011130.1|WP_057922396.1|4601867_4602893_-|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133039
NZ_CP011130.1|WP_148650738.1|4603643_4605077_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922398.1|4622334_4622865_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_046657745.1|4639078_4639768_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057922404.1|4635968_4636847_-|PhzF-family-phenazine-biosynthesis-protein	gnl|CDD|223461	COG0384, COG0384, Predicted epimerase, PhzC/PhzF homolog [General function prediction only].	9.28031e-78
NZ_CP011130.1|WP_036107789.1|4628787_4629375_+|DNA-starvation/stationary-phase-protection-protein	gnl|CDD|223854	COG0783, Dps, DNA-binding ferritin-like protein (oxidative damage protectant) [Inorganic ion transport and metabolism].	6.38771e-71
NZ_CP011130.1|WP_057922406.1|4639760_4641149_+|sensor-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.73094e-42
NZ_CP011130.1|WP_082648909.1|4641175_4642273_+|ABC-transporter-substrate-binding-protein	gnl|CDD|224753	COG1840, AfuA, ABC-type Fe3+ transport system, periplasmic component [Inorganic ion transport and metabolism].	6.94381e-33
NZ_CP011130.1|WP_057922397.1|4605656_4619555_-|hypothetical-protein	gnl|CDD|225750	COG3209, RhsA, Rhs family protein [Cell envelope biogenesis, outer membrane].	1.13226e-14
NZ_CP011130.1|WP_057923640.1|4620069_4622217_-|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase	gnl|CDD|223394	COG0317, SpoT, Guanosine polyphosphate pyrophosphohydrolases/synthetases [Signal transduction mechanisms / Transcription].	0
NZ_CP011130.1|WP_187313251.1|4635110_4635356_+|hypothetical-protein	gnl|CDD|370723	pfam09849, DUF2076, Uncharacterized protein conserved in bacteria (DUF2076). This domain, found in various hypothetical prokaryotic proteins, has no known function. The domain, however, is found in various periplasmic ligand-binding sensor proteins.	0.000582361
NZ_CP011130.1|WP_057922400.1|4624350_4628550_-|DUF3418-domain-containing-protein	gnl|CDD|273900	TIGR01967, ATP-dependent_RNA_helicase_HrpA, RNA helicase HrpA. This model represents HrpA, one of two related but uncharacterized DEAH-box ATP-dependent helicases in many Proteobacteria and a few high-GC Gram-positive bacteria. HrpA is about 1300 amino acids long, while its paralog HrpB, also uncharacterized, is about 800 amino acids long. Related characterized eukarotic proteins are RNA helicases associated with pre-mRNA processing. The HrpA/B homolog from Borrelia is 500 amino acids shorter but appears to be derived from HrpA rather than HrpB. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP011130.1|WP_082648653.1|4633906_4635031_-|collagen-like-triple-helix-repeat-containing-protein	gnl|CDD|374271	pfam15984, Collagen_mid, Bacterial collagen, middle region. Collagen_mid is the conserved central region of bacterial collagen triple helix repeat proteins.	1.78022e-09
NZ_CP011130.1|WP_057922405.1|4637579_4638563_-|glycoside-hydrolase-family-6-protein	gnl|CDD|376532	pfam01341, Glyco_hydro_6, Glycosyl hydrolases family 6.	8.97562e-63
NZ_CP011130.1|WP_057922401.1|4629688_4631506_+|DNA-helicase-RecQ	gnl|CDD|273594	TIGR01389, recQ, ATP-dependent DNA helicase RecQ. The ATP-dependent DNA helicase RecQ of E. coli is about 600 residues long. This model represents bacterial proteins with a high degree of similarity in domain architecture and in primary sequence to E. coli RecQ. The model excludes eukaryotic and archaeal proteins with RecQ-like regions, as well as more distantly related bacterial helicases related to RecQ. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP011130.1|WP_057922408.1|4642368_4642731_+|hypothetical-protein	gnl|CDD|178882	PRK00124, PRK00124, YaiI/YqxD family protein.	0.00259825
NZ_CP011130.1|WP_046657740.1|4631927_4633640_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	gnl|CDD|225387	COG2831, FhaC, Hemolysin activation/secretion protein [Intracellular trafficking and secretion].	2.31132e-67
NZ_CP011130.1|WP_057922396.1|4601867_4602893_-|glycosyltransferase-family-2-protein	gnl|CDD|133039	cd04196, GT_2_like_d, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.5596e-84
NZ_CP011130.1|WP_046657745.1|4639078_4639768_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	8.98414e-66

Protein sequences

>NZ_CP011130.1|WP_057922401.1|4629688_4631506_+|DNA-helicase-RecQ
MPSPALELLHRVFGHTAFRGEQAQIVQHVIDGGDALVLMPTGGGKSLCYQIPSLIREGCGLVVSPLIALMQDQVEAMRQLGVRAAYLNSTLSSEDAAEVERQLLAGELDLLYVAPERLLSGRCLNLIDRAKIALFAIDEAHCVSQWGHDFRPEYRELTILHERWPDIPRIALTATADEPTQREIAERLTLEDARRFVSSFDRPNVRYRVVHKDNGTRQLLDFLAGHRDESGIVYAFSRKRVESVAEQLAAAGIKALPYHAGIDAGVRAANQRRFLQEDGVVMVATIAFGMGIDKPDVRFVAHIDLPKSIEGYYQETGRAGRDGEPAEAWLCYGLGDVVNLRQLIQQGEAGEERKRLELRKLDSLLGFCESTECRRKALLGWFGEPHPGNCGNCDNCMEPPQSWDGTTAARKALSCVYRTGQRFGAGHVIDVLRGTATEKVTRFGHEALSTFGIGSDLDVKQWSSVFRQLVAAGLLEADIERHGALRLTADSAPVLRGERELRFRTEAPKAARASTRKTRGGAGAAPMIDMDPASLLRFNALREWRSTTAREQNVPAYVIFHDSTLRAIAEQAPDDLDDLGRIPGIGVSKLDRYGEAVLQHLLDHG
>NZ_CP011130.1|WP_036107789.1|4628787_4629375_+|DNA-starvation/stationary-phase-protection-protein
MAKVSKPGKPDKSSSKKSASPSSSNSPAASPAAGSSAPSIDIGISPGDRKKIAEGLSRFLADSYTLYLKTHNFHWNVTGPMFNALHVMFETQYTEQWTALDDIAERIRALGFNAPGSYAEFVKLSSIPEEAGLTEAADWREMVRQLVVGNEAVCRTARKVLDQADDVDDAPTEDLLTQRLQTHEKYAWMLRSLLQ
>NZ_CP011130.1|WP_057922400.1|4624350_4628550_-|DUF3418-domain-containing-protein
MNTSNSKHQSSYADASAALRQARNAIDGALSRDRGRLHGLWSRWSGKPADAQAQAAFAQALAASVAQREARAASLPRVPADPALPIAAEADRIVELIRKHPVVVIAGETGSGKTTQLPKLCLAAGRGAAGMIGCTQPRRIAARAVARRVAEELNTPLGEVVGYQVRFNDNVGERTAVKFMTDGILLAEIQSDRWLSAYDTILIDEAHERSLNIDFLLGYLKQLLKKRSDLKIIVTSATIDTERFAAHFDGAPVVSVEGRGYPVNVRYRPLDDAGMGNGESGIAGADRPVAGDASRNPKRIPNPESRISAMSVNDGIVAACDEITREDPRGDVLIFLSGEREIRDAHQALERRKYRETEVLPLYARLSVRDQDRVFNPGPKRRIVLATNVAETSLTVPRIRYVVDPGLARVKRYSPRGKLDRLHIEPVSQASADQRKGRCGRISEGTCYRLYSEPDFESRPRYTDPEIRRAALAGVILRMLSLGLGSVDGGGHKRRGPRGAAATTEQDAATAHGASARIIEDFPFLDPPDSRAIADGWQQLAELGAVDEQRRLTAIGRTMARMPVDVKLARMLVAANAHGCLREMIAIAAFLGIQDPRERPADQRGAADAAHALFADPRSEFVGILKLWDAYQTAHEDLTQSKLRGWCEKHFLGFLRMREWRELHRQLKLLCDELGWQAQASSGELDASAYATLHRALIAGLPTQIGFRGDKGLYDGPRGRKYQLFPGSPLAKKPPPWLLSATLLDTERVWSMTNATIEPDWAIQELPHLLARRHHDPRWARSQGRVVGSEQISLFGLVLAPKRPIHYGALYPEESRIIFARDALVTGEINTRAAFVARNLATLAKAHEEEAKQRRAGLVVDEEWMAQWYLDRLPAQIHNVQAMDAWYAKLPADEKRALEWSNNDLMVGGETEASRFPPYLQLGNARLAVRYRFEPGAVDDGMTVAVPLHLLNALDPAQLSWLAPGFVADKAAALIKSLPKTLRRNFVPAPDFAKAFHEAHRQAEADDLVSVLARFLRKLTGTEVAATDFDPSTIEPHLRINLRLLDAADPRGGKDAERKVLAESRDLDELRQRFGERAARAFAAQAADGLGQQGLTAFPDQPIPMSVPGAAGVPAFPALHDDGDTVSLRVHAEREAALRAHPGGVRRLLAIAMAEKLKQARKQMPIQAKTGLLYAAIESAAPRKDRVSPTRAAQDRASHDRPRDSDRLREDLVDGALQSLLGDDADLVAVRDPAGFELRRETVARKLFPEAMERLRQAETILGAVAEARARLESSLMGWASGNLDDMRAQLARLTPPGFLRDVATSALAEYPRYLKALSVRSERALRDPVRDQARMLELKPFVDAFDAAQAAGLAEDAGWQALRWEIEELRVSLFAQELGVRGGVSPKKLAQRLAGLRG
>NZ_CP011130.1|WP_057922399.1|4622919_4623405_+|hypothetical-protein
MRAFAPLSLAVLFAVSAGASAAERHYVPVEQRFSAEQMQATGLSSLSPAQLTLLNELLSQDQTKAVAEAERKIQAERNDPFSKVAADPIHSTIKGEFRGFSGGNVIVLDNGQRWRVIDGSLFIGKPVTSPKVTIKPGMMGAWYLEVDGQIPKAKVKRVDGG
>NZ_CP011130.1|WP_057922398.1|4622334_4622865_+|hypothetical-protein
MSAILLSTPRPALSRLLIAAAIALTLAAPAALAQSKIEQQMSAEQFKAAGLDQLSPEQLSNLNAWLNRTLDSETSKAVVKAKEETRAQVKHENRGFLGSGSREAVVARMTGPFNGFSRGQTYILDNGQEWRQDDNADLPGVHLDAPQVRITPSVIGNTWYMAVQGYNTRAKVTRTK
>NZ_CP011130.1|WP_057923640.1|4620069_4622217_-|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase
MAQPAAAALAAPLRKALLEAAQAPQAGANALDAPAVVAATLDALALLDADSDTVAAAILHAYPGWASAMGAGFERDYPVVAALLDGQRAAGQVWALHAEQGRHSGTEGLRRLLLAIVRDLRVVPILLARQLARMRHADHLPADTRRELAALTRDIHAPLANRLGIWQLKWELEDLAFRYLEPQTYQKIARLLDEKRGDRERYIEQVKRTLREAMSAQGLKAEVAGRPKHIYSIWKKMQRKDAPISELYDLRAVRVMVDDVGACYAALGVVHATWTPVPSEFDDYIARPKRNDYRSLHTAVIGPEGKTLEVQIRTHEMHRQAELGVAAHWKYKEAGSHSADAAFDRKIAWMRRLLDAKGDGGQGGDEALASELDTELVEDRVYVLTPKGEVIDLPTGATPLDFAYHVHTEVGHRCRGAKVDGRIVPLDHKLRSGDRVEILTAKTGEPRRDWLVLANGFLASNRSREKVRNWFHKLDRSRNETAGRELLDKELRRLGLLGADLAPARERFTLASDGDLYVQVALGDIGPHQIGRALLEHERAQAAPPPAATHASGTTVVTPPAPRKVPGKSTDFTVEGVGNLLVQLARCCQPLPGEPIVGYLTRGRGVSVHRPGCQAFERLAAATPQRVLPVEWGRKGSGYEVDIEVLALDRKWLLKEVTNVIAQSNAHVLSIRSDVERNGAQVRLRLRLRVADYGQLSTLLGKLSSLPAVEYAQRQ
>NZ_CP011130.1|WP_057922397.1|4605656_4619555_-|hypothetical-protein
MAAVISGSGLGLFNSSFSQIGKGLGASARYGQGQDSQYVNIATGNLLLHSFDDQVVMRGMTVGFSRTYNSRGTFADAGNDAWLTGFERRIELIGTLNQAGSVMRRHSGDGSYQDFAYAGNGLYRSTVGDGAHDSLRRDGKTLQWLYEEGDTRLEETYADPATGGRLTRIRDLKSDPQQPTTWNLSYDPQGRVTEVAANDGNGNLSRMQFTYAGANLASVTSYSGGQAVGRVWYGYDAAGRLSTVTHDLTPGKTGDDEWSATAAVNDGHLFRTVYSYVDASSLQIASVQHSDGGVVSYTYDALGRVRTLTRGDLNDNDADGQGQTLSFAYDTEARSTRVSDSTGRTWIYYYDESNQLIAAEQPSAGGWQETYTYEYDADGNLTAAMVDGAAGRVYRHDANGNAIEQREFISSGLRVITRVTERSFNAANQITSETVYEVDEGDILGRASASAGAGSETGKNEALTPPANALITRYIYDAANRLRFVVNAAGEVSESEYASAGFGIGRILKARQYLDATYTGAYTLAALEAWAGAAPRKANSGLTQYSYDAFGSVAWRRYAAVDAAGNGIAGDADLIEGYRYDERGRVLERNASSGADLRRTVYVYDGMGRLLAEKVFDRNALALQSRSWAYADSQRLATAIVEGGAVDDGDISNDRVRIEQRDAAGQVVLVSERALGGPTTTRETRNLYDRAGLLRAVQDANGGRSYLFYDVERQLVGEVDATGALVEYVRDTFGRIVQTVRYATVLDTRAWMPAPPASPDLAQVPTDIALVRPTATPQDRTVTTFYDLLGRKTVETDGEGRVTYFSYDLNDRLIRTRQLPRANAPQNEERITRYFYDAMGRELGRLDAEGYLVEHNYDLAGNRTRSVAYASAVASNLREATLGQMRPAATAQDQVTLWFFDGRGNTLAMLDAEGYLTQYLRNERLAQDTTRAFETQLTGLTGTETLATLLSRAQAGRVRETRRGYDALDRLIVQTDPEGTVTRNTYDAQDNLVRTELAADTSEVREGRLRYNVFGELIGELGGEGTTRLRPDMTQAQIDAVFAQYGTRHGYDGLGRRIESIDADGHKTWYFHDADGRPTYTVRGLPGTSGLLNARGEVSQVRYSAFGDAVETTAYTGLLTIAVPGDRDSVATALTTLAYTAASDSRRSYSYNRRGQLAEVRDAENAVLRYSYNGHGDRTVEQRAFGTALELRIDSSYDNRGLIKTRIEAPNTVLQRQLSWSYDAFGRVVEATDARGAPTTFGYDRLGRQVSRSQTVQGRAETWTSNYDAYARVLSQTDPNGRSTSYFYDTAARSMRVTTPEGVEVTTAYTRHGQQLSVSQAIPGGGIAVTSYRYDRDGRLLSVTDPLNKQAVNEYDSRGLLSASVDASGRRVELRYDAVGRVLQRIEDPQQLALTTSYVYDGQGRSQRVTDASGRVVQHRYDREGRLLETALDPDDLNLRTGYSYDAHGRQLTVTEGAGTARARTVRYDYDVLGRRIGEVVDPAGLALTTGYVFDANDNLLRRYVIDEGSQRYTQRSYYDEANRLIYSVDATGAIVRRWYDPAGREVATRAYLDATAPAGLSDTTTLAQLHGLSIEQAGDQGSYIVYDGDGRVRYRIDLHGRISESRYDVAGRLASELNYSNAIAVSDALRHRLRAGTVPPQDIAALIVSNDARMVRHVYDAVGRERYTLVQDSASTATVSERRFDDSGRVVAENLYGVRIPISTALTEAAVTTALGIAGGTGNLRQTRYVYDQAGRARYTVDDAGAVVAREYDEAGRVTVVREYEGLIAAATPMTETGLSLAVAGMRQRMTVTRYDNAGRVERVTDAAEQMERYTYDASGLLIELLDRNALVWTYGYDGAGRRVTETSPRVDVSTIDADGVVSTQNRSIVTRTNYNALGQVLSRSEDDGTAQARMTHYEYDAAGRQNRTVFPLAGRIDPATGALDIGGTRPSTEVGYDSLGRAVVNKDVSGRYSYKVYDDFGQLYLDIDPAGYVTRYEYNVFGERTGLYRHATAFNFGALSGWSAGHAIGYAQSINGVVYDAAKDRGIATIYDKRGQVARVEQSPLEYYRDDGTAATGRPTTAYEYDAYGRKVKESVLLQGTRGQSDARWADSYFYYDDLGRLVLSVDAEGYVTANEYHPTGELKRRIEYARAIATSNLSAATPPSLPASGDDIVGFDRITRWEYDPLGRKHREYMQRHFADSQGSSGVREVMSQFEYDGRDRLIRLSDDTGVTSTVYDALGRAINLTEPARNVLAANADSQLLNGVDLAVGTLYAWASPYTQMRYDAFGNVIETRRYANGLRAGAAVADDQRDQIERVRYDGQGRAVVVFVKRETDTGAGIASGNRTYLIYDDADRIVERWSVLDTDLAGGAVRVHDRFRYDAAGRQLESQRTRESAAGAVLATDLLETVGYNAFGEIVSKQYGDVAGVLDYRYDLAGRLLSDNETGAIRSYGYNLAGHRVREAHFVLGAAGVESAVTRFGLDRLGRTIASELPAYQDGAAPKPTTSRQLDRWGNVLSIVDTRGYRTDYRYNERDQVTRDERPLVEVVSESGVRQWLRPVNQWFYDALGRLVATRDANGNTRTNEYDATGRMIASADALNQKTLFAFDVLGNQRLTQNPMGYLTYKDYDNQGRIVGIGDYLPTSAGIARERKSLQRYVLNQNGDRNGLYDALDNLVRYRYDSAGRVVRSQSASGAVSTYGYDDQGRKTAEFNGIDTMSWSYDVQGRLIAHRNLGGRDLGNEYDPVTGQLVNERQTGGAGLDVVDGARRTTYYPDGRVKAVYEQGSATPSYRYEYDAAGNRVVEEVDTRDASGRLVRTRTRTVYDSNNRIQRVYTDELGSGGTPTKRIFDLSYSYDAAGNRRSVRASSGYGPNATGVGAENTRPQVVQTPPARWLRSGQNAEFSIVFSDIFRDAEQDALTLGIGRADGLPWPSWLQLSGPDANGQVRFIADPPAGTVQQIEIRLSATENRPGGLSEATSFVLSVGANRAPTVIDTVQPVLRAKTGQPWGRDLLASDYFLDPDLGDVLRLELESASPPTSDWLSAAPDGGLLRLRSTLTPATPGDYSLRLRATDQGGRTAIKTVVIRVVASTAPTGPNTLPPRAATLGREFEWSMPLASVFTDADGDRLSIGTIGLPNWLSFQQTNEQGQPQLRLSGHAPDDVAAGHVYTFQFKASDESGNSKLASLSITLRAFNTDPYLGGTINDAQMVLIRDGSYYPPPLPAFLDSDGDAVSVRLTGLPPGLSFDPVTRQIGGNAPLGTYWLTYSADDGRGGSVSQSLRVIVRDNTPPTVPAFTPPNPRQGAAYRYVIPESFDPDEPVDYWVNAQQLPPGLSFNNLTREITGVPTAQGSFNVTMSVWDRFGATTVTSFAMTVSAPAANQPPVATVPSASLIFEMTSSNSAPPDLTLDAGLFVDPDGNPMSYTMSGHPSWLRHEFGPDGHVFRADTSAWLAQSSSFTLTADDGEEGRTALNITVRVRRTTLLEQPGIDPPVESFEFDMGTGLPPHDQKADSGIEPGVVEPGVIEAAVPVETKEYWYTYDAENRIKINNGVLQGGQIVLTHAEPESYELRYDAAGNIVARFSLRLAGPGATVPTLRVERSVYDLRGNRQIEFHQQVVGGGVDAFQGVRQRFEYDANNRLIQAREYYANSMNFDIGVDGAEWISLGGWLSAAEVYVYDIDGRLISLDTKGRAALNVSWIRPAHNNNLAAQYTDLGVLQAKTYADYRINTGRQPNGPVADIRATGYDAAGRLVRYDYSPDASYASTQRYSYTYYGWDSYQEKTVTGTRPAQPAQPSTTNTLTYDSFGRLRSQLEHTRLSSGSIEDRMRYYSYDGDGRVQTRREGVMRGGVFTQDGAGGPGNYFLVHAGGQQQAELREGVQLSSGLPSRQIQSLGGRGYYQAGGDTVIAQPGDTLRSLAQRVYGAEQLWYLLADANGLGDPDQELAAGTQLTAPDTTVAHNDASTFKPYDPAAAIGPTAPGLPMIAPPPKNHCNAVAMVLMVVVAVVVSVVTYGALAAPAAAWVGSATGGAILAGAAAGAASSVASQAVGSATGVSSFSWRNVAASAIAGGITAGIGATSFGEAMKTTTQGRAALAAIGSAANYVGQKVAGLDTAFSWRNVAASAVSAAVSSKLNGALGLEGEGFAVGFGANLTEGVVSLHVRQAFGVDGAGDYGRIALDAFGNALGNWVASNAGGGAKTLEARLSKSMAATQHRLDAEIERDTALSVGADLDRRFAGLAASADMRLSAAIDMQADARVNMLQWSRQNFASTQADLYAVVGGRGRLAAASFASMAVSASGGGVVAVGDIDAMVESLPVDQNPGFYKDDSIVRRNLAEQLEHARNAGVLERASWYLSEHRGRVGEPEGLTDARRELRAFEQAPDFIPLQAVQDYYGRMMAYDAGELEMSAQEAARLRLTLNAFNRFYMGDTPLPLAGQSEAETEAQRRFANDVGMSFLGVFALPAMLTRAVGGNETRVGAALQAGAVVLDLYSSRSGSARGPLRLASRSRTGRQDIPGSRLGKLSGEYSAMNPGPLDDGMAGTFAGGRYKAVVLDKDTVLYRAGTQSQPLGQYFSRQSPLGVLQTRIDKAVLPQWPGGGKSPIDTVFAVKIPAGTEVYVGKVGTQGGFYVGGTQQIVVRKPWQIDGVQVIDWKPLK
>NZ_CP011130.1|WP_036112801.1|4605384_4605660_-|hypothetical-protein
MTELREIQALLDRMVDLLNLAAQPDWAGALERHREAIGTAPDITKARILAMYGGMGSLNDVVLYKNGQPLSRENNEFDELRIRLHELCRAT
>NZ_CP011130.1|WP_148650738.1|4603643_4605077_-|hypothetical-protein
MPLLVLALIALIPLRQPLSDRLWPESRLQALHQQAAQALSEGKLTAPDGHGARELYEAALALDPDRGDARQGLARVGAMALVQARQAIDGGHFDFARERLELARELATPRDQVEALARRLREREAAHAGLDRLVAQAANARAQGRLDGAPDAALPLYLRVLELQPQRNDALEGRDDTLADLLQQARQALEHGELARGAQGIARVQAADPGHADLPDALSVLERHIEQRRRDADQALRRQRLDRAAEAYRDLLAIQPGDEAARRGLISVANAHAALSERYAADFRFADAQAELERARELAVDAPAVTLAHQHLDRARESRKRFDQEPLLARRQSLRRLLNEAAAAEQRGDLLTPPGDSAYDKLRAAQAIAPQDPAVRAAAARLLPAARRCFETELSSNRLVRASECLDARRALEGASAPVREAATRLAQRWIAVGDERLGAGELHAARSALDSARRLDPGANGLSELAARVQAAAAAN
>NZ_CP011130.1|WP_057922396.1|4601867_4602893_-|glycosyltransferase-family-2-protein
MALNPRPAPDSVAVVLCTYNGARYLPQQLDSLLAQTLAPQRIVIADDASSDDTWTLLEAFAERARARGIAVDLQRNPRNLGYLRNFEAALRRAEEAIVFLCDQDDVWYPNKLADYLEQFRARPRLNLLHSDSRLIDGEGRELGRRMFQTLEVSAAELAAIHAGRGFEVLVRRNIVTGATTALRREVLAQALPIPDAEHPELERSAWVHDEWLALIAAATGEIDCVEAPTMGYRQHGGNQIGARQRSLIERLGGGKQRREHMQAMVAKLDSLRAHLQRAGLDVGVAKRAAIDARIAHLRLRLDLPANFARRWPLVREEWRHGRYLDYSAGLRSMVCDLLGLR
>NZ_CP011130.1|WP_046657740.1|4631927_4633640_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein
MDTGLWGKRYPLALAITAMLAATTAHSQTQPRLPTTGNPLQTLPQAPLPKAEPKVGTIVAPQQNPEMAALLAVPLTPIRFEVSGVKSVPFEQVTGLFIPLIGRQITVADLLGAAETCTKLYRERGYALSFCYVPTQDFADGTVRVVAVEGYVAQVRIGGKPGKLERKIRAIAQRIIDDRPLRQSTFERYSQILGFLPGAKMTINVPAPTTTDGATSLDLNVGGKRYDATWALEFNHPGTQGLATLNLNALTSLAEQWSLAALYPDGRSNERFYSAGYSQLIGSDGWIGRVDGSRYRGVPVTQTPLPAFLDHRVEQDRVAISARYPLLLRNERSLFVSAGVYAADQSDRYFNTINGALLDQRSKTRVVTAGLDYAEAKKNHARQASISIARGLDTWGASADTVTNIDGVDVAGASDVSFTRYNLGYAQSRTWKEQRYAAVLRATAQYSRQRLPSSEQISFGGSRFALAYDPGETSGDRGWGAALELSRNFRPKAKWLKSVTPYLSVQHARVSLTEGRPPIDDLGSVALGLRLSDNKHFNVDFAYAKPTADIPLETDDRKPRWNLNFSYQLQ
>NZ_CP011130.1|WP_082648653.1|4633906_4635031_-|collagen-like-triple-helix-repeat-containing-protein
MPGNALGAIVTVAGNLVTGIGGGVSTLGAQIPNQALLGGNNPTTQGLAKVVDDLGKTVSGLGLSTSSGLGQIGNTSNPVGTTVGGVDNLVVNVGTTVDDLGKTVATVGAFQGSPIQPLTSAAGGLVSGVGGGVKDIGGKLGGVLEGSAGQSLTGAVSSVLTPIAGLGQTNGGGTGGSGGGNLVANVSQGAGGVVGGVASAGAALGGALSGAPVPGGAAGLVGGAVTGVSNNLGTVGAGITAGLGNAGSIANPVGVTAAGVTSGVAGLGGTVGGVGAGVASVGGSTPLAPVTGLVGGALAGVGSGVTTVGTGATAAVNGPLQPVTQGLSTVVNGVAGATGLNNTNGGLLGGVLGNDSGKGGLLGTGLLGKKGGKP
>NZ_CP011130.1|WP_187313251.1|4635110_4635356_+|hypothetical-protein
MPGPPGPPGPPGLPGPPGPPGLPGPPGPPGPPGSPGPPGPPGSPGPPGPPGLGLKLDLTPPEPEQPVVETVTVKMHAANKL
>NZ_CP011130.1|WP_057922404.1|4635968_4636847_-|PhzF-family-phenazine-biosynthesis-protein
MTLRRYLQLDVFAHRIGAGNPLAVVFDAQDMDAAAMQSFAAWMHLPETIFLLPPQAGADYRVRIFTPRQELAFAGHPSLGAAWAAIDARRVPADRESLVQECAAGLLPVRVVHDSTGMRVSVRAPRARRCDHDRATAPRLDAALAGWPRGALAPALWDNGPRWWVVELEAAPDQPDPVRSLQPDLNAILALAGDDALGLAVFARSRDPGYDYVVRAFCPSDGIAEDPVTGSANAAIAAALVEAGRLRPGDRYSVSQGREVGRDGCVEVRIDEDGEVWIGGQVQAVIRGTVEW
>NZ_CP011130.1|WP_187313252.1|4637187_4637358_-|hypothetical-protein
MRSFPRRPVVHRLWLTIVCQTVFFSSVVLSVDRGALRAADDAAPAMHERGVPSARR
>NZ_CP011130.1|WP_057922405.1|4637579_4638563_-|glycoside-hydrolase-family-6-protein
MRQIFRSNSAPPAARTRRVFATLALAAALTPACALAANQNSGFYVDPDSNPAVWARDHPADTRANAIRNSIATRPMARWFGNWSGNIGTAVTVFVDAARAADKLPILVAYNIPGRDCGSHSGGGAGSPEAYRTWISSFASGIGNRRAVVVIEPDALAQLDCLAADQRSVRIGLLQHAAREFKARAPNALVYHDGGNASWIGADEMARRLNSAGARDLRGFALNVSNYHTTADSNAYGAAVAASLQRQFGYSKAFVVDTSRNGNGSNGEWCNPGGRKLGAGSQNSATGAEMLLWVKVPGDSDGKCGIAPNTPAGEFSPDIATRLIEGR
>NZ_CP011130.1|WP_046657745.1|4639078_4639768_+|response-regulator-transcription-factor
MRILLVEDNLDLAHAVVQHLRRGGNAVDHEADGLSACRFLEHERYDLVLLDIGLPRMDGLSLLAELRRRGDATPVLMLTERSDIEDRISALDVGADDYIGKPFDFRELSARCRALTRRRQAQTSALVRIGPMTMDNAARRLRFHNRTIDLPNREYSLLEILVGRLGQVVSKNEITNRLFALSEEAGSNTVELYVARLRKKLPRDFLRIVTVRGTGYLAETTHGNGMAHD
>NZ_CP011130.1|WP_057922406.1|4639760_4641149_+|sensor-histidine-kinase
MTELEQARPSIRRTLLLSIGLLSLVGMLLLFFGARQYGRRAADLSYDRLLNASALTIADSITLVDGQWEANIPCAALELLSAAPDDRAFYRVFLVGGRTLTGYDDLPRPPSLAADHSVFFDADYRGEAVRFAVLRRAASSADGPEAALIQIGQTRRARNEVAGDIVWHVTGWIALFTVAILLLARLAIDRALQPLARIEQDFSVRTPFDLRPITRAVPTELSHVVAAQNHFMSRLSSNIDALRAYIAEAAHQMRNPLASLRAQAQLALDQNSPQQWRQGLVAVERHSDKLGRLLNQLLSHASVTHRAELHHFKPLDLRTIAKQALRESVPQAEPRPRVRFDCDADDTRLHGDALMLREAIKNLIDNAIKHGGSEDAPILVRLHADGAGLLLSVEDAGPGMSAEQRERAFDRFDRGEHASAQGAGLGLAIVKRVVESHGGRVVLDTSASGGLSVRLHLRRDAA
>NZ_CP011130.1|WP_082648909.1|4641175_4642273_+|ABC-transporter-substrate-binding-protein
MLYLVAAIGTLYLGHAQARPPQSERIAVFDAAIARQGRLVLHGSSNVGLVRALIEDYQRLHPAVEVRYSHLDTAQIYARGARAGAAQERPDLLLSSSTDLQIKLVNDGYALAHRSPQVQALPASARWRDEVFAYGYEPVVMVYNRERLDPQRAPQTREQLRRLLRDPHGPLRGRIGLQDPRDSAVAYFIATQEAKLLGNDAGPMLTALGENDARLFKRMDPLLDRLSDGEIGFAYGVFGSYALQRIERGAPLRIVLPRDHLLLVARTALIPRAAPNPAEARRFLDYLLSPRGQVLLAREAKLIPARDDLPDPPRLYGDLSQRSAALRRTSLGLGFLVYLDEVKKRRFLRDWIEHLAPTEAAVPPR
>NZ_CP011130.1|WP_057922408.1|4642368_4642731_+|hypothetical-protein
MPRPRPFIAFAIALSLTAFGAHATELGESPFSLRSAEPGTVRALAVARAEFVKRLALEAGPDPADDATTRQADDFDIAITQDADHYRVDFAPSQRGYRGGGYGYLIAKDSFRVVERRIYP

Crispr_ID: NZ_CP011130_16

• CRISPR_ID: NZ_CP011130_16
• CRISPR_location: 5199356-5199435
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP011130_16

Consensus_repeat	Method
TCTGGAAGGATGACGCTGAAGTCTCTG	CRISPRCasFinder

spacers of NZ_CP011130_16

>16.1|5199383|26|NZ_CP011130|CRISPRCasFinder
GATTCCCGCCTGCGCGGGAATGACGA

CRISPR arrays and Neighbor proteins around NZ_CP011130_16

CRISPR arrays

The CRISPR arrays of NZ_CP011130_16

>merge|NZ_CP011130|16|5199356-5199435|CRISPRCasFinder
TCTGGAAGGATGACGCTGAAGTCTCTGGATTCCCGCCTGCGCGGGAATGACGATCTGGAAGGATGGCGCTGAAGTCTCTG

>NZ_CP011130|16|15|5199356-5199435|CRISPRCasFinder
TCTGGAAGGATGACGCTGAAGTCTCTG	GATTCCCGCCTGCGCGGGAATGACGA
TCTGGAAGGATGGCGCTGAAGTCTCTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057922694.1|5191014_5191599_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922702.1|5205538_5206546_+|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273386
NZ_CP011130.1|WP_036114817.1|5189956_5190925_-|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP011130.1|WP_057922699.1|5198256_5199195_-|hydroxymethylbilane-synthase	unknown	unknown	gnl|CDD|234612
NZ_CP011130.1|WP_057922698.1|5197376_5198051_+|DUF481-domain-containing-protein	unknown	unknown	gnl|CDD|225679
NZ_CP011130.1|WP_057922697.1|5196239_5197187_+|dimethyl-sulfoxide-reductase-anchor-subunit	unknown	unknown	gnl|CDD|113736
NZ_CP011130.1|WP_057922695.1|5191991_5195021_+|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl|CDD|239164
NZ_CP011130.1|WP_036114855.1|5211241_5211823_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036114833.1|5195321_5196131_+|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl|CDD|319873
NZ_CP011130.1|WP_036114843.1|5199550_5200285_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225818
NZ_CP011130.1|WP_187313263.1|5202342_5203332_-|TonB-family-protein	unknown	unknown	gnl|CDD|367555
NZ_CP011130.1|WP_082124743.1|5200305_5201292_-|histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP011130.1|WP_057922701.1|5204219_5205542_+|TolC-family-protein	unknown	unknown	gnl|CDD|224455
NZ_CP011130.1|WP_148650541.1|5203674_5204091_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923683.1|5206598_5209823_+|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	unknown	unknown	gnl|CDD|129992
NZ_CP011130.1|WP_057922703.1|5209949_5210846_+|cation-transporter	unknown	unknown	gnl|CDD|224151
NZ_CP011130.1|WP_057922696.1|5195103_5195325_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922693.1|5189018_5189957_-|patatin-like-phospholipase-family-protein	unknown	unknown	gnl|CDD|132866
NZ_CP011130.1|WP_046658041.1|5201388_5202090_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|334855
NZ_CP011130.1|WP_036114820.1|5191653_5191869_-|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP011130.1|WP_036114817.1|5189956_5190925_-|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	8e-65	214.1	3.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057923683.1|5206598_5209823_+|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	gnl|CDD|129992	TIGR00914, Nickel-cobalt-cadmium_resistance_protein_NccA, heavy metal efflux pump, CzcA family. This model represents a family of H+/heavy metal cation antiporters. This family is one of several subfamilies within the scope of pfam00873. [Cellular processes, Detoxification, Transport and binding proteins, Cations and iron carrying compounds].	0
NZ_CP011130.1|WP_057922702.1|5205538_5206546_+|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl|CDD|273386	TIGR00999, Nickel-cobalt-cadmium_resistance_protein_NccB, Membrane Fusion Protein cluster 2 (function with RND porters). [Transport and binding proteins, Other].	1.87186e-29
NZ_CP011130.1|WP_036114817.1|5189956_5190925_-|YafY-family-transcriptional-regulator	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	1.19115e-55
NZ_CP011130.1|WP_057922699.1|5198256_5199195_-|hydroxymethylbilane-synthase	gnl|CDD|234612	PRK00072, hemC, porphobilinogen deaminase; Reviewed.	4.3537e-164
NZ_CP011130.1|WP_057922698.1|5197376_5198051_+|DUF481-domain-containing-protein	gnl|CDD|225679	COG3137, COG3137, Putative salt-induced outer membrane protein [Cell envelope biogenesis, outer membrane].	4.55702e-07
NZ_CP011130.1|WP_057922697.1|5196239_5197187_+|dimethyl-sulfoxide-reductase-anchor-subunit	gnl|CDD|113736	pfam04976, DmsC, DMSO reductase anchor subunit (DmsC). The terminal electron transfer enzyme Me2SO reductase of Escherichia coli is a heterotrimeric enzyme composed of a membrane extrinsic catalytic dimer (DmsAB) and a membrane intrinsic polytopic anchor subunit (DmsC).	6.41575e-33
NZ_CP011130.1|WP_057922695.1|5191991_5195021_+|molybdopterin-oxidoreductase-family-protein	gnl|CDD|239164	cd02763, MopB_2, The MopB_2 CD includes a group of related uncharacterized bacterial molybdopterin-binding oxidoreductase-like domains with a putative N-terminal iron-sulfur [4Fe-4S] cluster binding site and molybdopterin cofactor binding site. These members belong to the molybdopterin_binding (MopB) superfamily of proteins.	0
NZ_CP011130.1|WP_036114833.1|5195321_5196131_+|4Fe-4S-dicluster-domain-containing-protein	gnl|CDD|319873	cd10551, PsrB, polysulfide reductase beta (PsrB) subunit. This family includes the beta subunit of bacterial polysulfide reductase (PsrABC), an integral membrane-bound enzyme responsible for quinone-coupled reduction of polysulfides, a process important in extreme environments such as deep-sea vents and hot springs. Polysulfide reductase contains three subunits: a catalytic subunit PsrA, an electron transfer PsrB subunit and the hydrophobic transmembrane PsrC subunit. PsrB belongs to the DMSO reductase superfamily that contains [4Fe-4S] clusters which transfer the electrons from the A subunit to the hydrophobic integral membrane C subunit via the B subunit. In Shewanella oneidensis, which has highly diverse anaerobic respiratory pathways, PsrABC is responsible for H2S generation as well as its regulation via respiration of sulfur species. PsrB transfers electrons from PsrC (serving as quinol oxidase) to the catalytic subunit PsrA for reduction of corresponding electron acceptors. It has been shown that T. thermophilus polysulfide reductase could be a key energy-conserving enzyme of the respiratory chain, using polysulfide as the terminal electron acceptor and pumping protons across the membrane.	1.2845e-75
NZ_CP011130.1|WP_036114843.1|5199550_5200285_-|response-regulator-transcription-factor	gnl|CDD|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	1.11079e-61
NZ_CP011130.1|WP_187313263.1|5202342_5203332_-|TonB-family-protein	gnl|CDD|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	8.17329e-13
NZ_CP011130.1|WP_082124743.1|5200305_5201292_-|histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.16406e-44
NZ_CP011130.1|WP_057922701.1|5204219_5205542_+|TolC-family-protein	gnl|CDD|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	1.27728e-19
NZ_CP011130.1|WP_057922703.1|5209949_5210846_+|cation-transporter	gnl|CDD|224151	COG1230, CzcD, Co/Zn/Cd efflux system component [Inorganic ion transport and metabolism].	5.24934e-114
NZ_CP011130.1|WP_046658041.1|5201388_5202090_-|alpha/beta-fold-hydrolase	gnl|CDD|334855	pfam02230, Abhydrolase_2, Phospholipase/Carboxylesterase. This family consists of both phospholipases and carboxylesterases with broad substrate specificity, and is structurally related to alpha/beta hydrolases pfam00561.	2.32863e-54
NZ_CP011130.1|WP_057922693.1|5189018_5189957_-|patatin-like-phospholipase-family-protein	gnl|CDD|132866	cd07228, Pat_NTE_like_bacteria, Bacterial patatin-like phospholipase domain containing protein 6. Bacterial patatin-like phospholipase domain containing protein 6. PNPLA6 is commonly known as Neuropathy Target Esterase (NTE). NTE has at least two functional domains: the N-terminal domain putatively regulatory domain and the C-terminal catalytic domain which shows esterase activity. NTE shows phospholipase activity for lysophosphatidylcholine (LPC) and phosphatidylcholine (PC). Exposure of NTE to organophosphates leads to organophosphate-induced delayed neurotoxicity (OPIDN). OPIDN is a progressive neurological condition that is characterized by weakness, paralysis, pain, and paresthesia. This group includes YCHK and rssA from Escherichia coli as well as Ylbk from Bacillus amyloliquefaciens.	4.8295e-60

Protein sequences

>NZ_CP011130.1|WP_057922699.1|5198256_5199195_-|hydroxymethylbilane-synthase
MKTLRIATRKSPLALWQSEHVADRLRALHPGLVVTLVPMSTRGDEVLDRSLAAIGGKGLFLKELELAMLREEADCAVHSLKDVPMELEPGFAMPAILERADYADAFVSNAFDGIDALPTGARVGTSSLRRQAQLRALRPDLELRDLRGNVNTRLGRLDAGEYDAIILACAGLQRLGLDARIRARLESPYWLPAPAQGAIAIECREDDLSTRELCAALDHAATRTCVEAERGMNRALHGSCHVPVAAYARLDGEHLRLDGQVGSASDGRAVRAHGEGRGDAPECLGIEVAQKLLEQGAAEFIADSLGDVGDQD
>NZ_CP011130.1|WP_057922698.1|5197376_5198051_+|DUF481-domain-containing-protein
MLGAIGLALLGAPLVTLPTPAFGGDPILIAIASDPAQMRLYCFSTRCGDEEWKLAMARRQRAPEIDPADLPPLRKVELPGQQRVIGGVSAPATSRESRSMYSNDYRIGTRYGVQAVRDGPTQIGLQFGAGYRLAPLYDDGINRPGAVFRGELNLGQRIGDRARFTQSVQVESGRGDTFVKQSVRLDVEVWQNWKLETDFAIRHDNNGGGGSESAESSIELIRRF
>NZ_CP011130.1|WP_057922697.1|5196239_5197187_+|dimethyl-sulfoxide-reductase-anchor-subunit
MHPAFSVIFFTTLSGAGYGLMAWVGAIAFYHYAGGSLVEPMRALAFAMLTALILVTVGLLSSTLHLGKPLRAWRAFSQWRTSWLSREGVMAIVAYLPALGLLLGVVRKSGAAMPMLLSVAVVVCALLTVACTAMIYASLKPIPAWRHWLVVPGYLAFALLSGAALLAALPATAAVERSAMTAVVLLAPLTALLKLMYWRAIDRTSLPVTRGEAVGLPDRELSVFERPHTEENYLTREMGYVLARKHARKLRLIALTLFALLPVAGMFVAGLMQVTGSPETAAVVTALSALSVLLGAVVERWLFFAQAKHLVTLYY
>NZ_CP011130.1|WP_036114833.1|5195321_5196131_+|4Fe-4S-dicluster-domain-containing-protein
MTGLPPPSKKKLGLVIDLDTCVGCHACAVSCKEWNAGGFSAPLTDEQPYGKDPSGVWFNRVHSYEVEATAVAALPIADPVRGCGSAAAVDTAPQPAMTLHFPRSCLHCEQPACVTVCPTGASYKRAEDGIVLVDEDKCIGCKLCSWACPYGAREYSPVEGVMKKCTLCIDRIYNENLEESERQPACVQACPTRARHFGDLADPESKVSKLVAERGGVDLMASLGYQPTNKYLPPRARRAGAAEPAPAAETLDTQALPTVLRWLDRVLSR
>NZ_CP011130.1|WP_057922696.1|5195103_5195325_+|hypothetical-protein
MKPVRVFAGLLCIALSFGLVLLLGLGMFDPTRDAAASANGSVTPVLIALMPSVTVGLAVFALGVWLISTGRKR
>NZ_CP011130.1|WP_057922695.1|5191991_5195021_+|molybdopterin-oxidoreductase-family-protein
MREHAPSEPAIDLSPSPGDEVKTTTCYMCACRCGIKVWLADGKIRYIQGNPDHPVNQGVLCAKGSAGIMQHYSPARLSKPLLRVGERGKGEFREIEWDEALGIAAGWLGPIRERNPDELAFFTGRDQSQALTGWWAQQFGTVNYAAHGGFCSVNMAAGGLYTLGGSFWEFGEPDWEHSRYLMLWGVAEDHDSNPIKLGLGKLKARGAKIVAVNPVRSGYGAIADEWIGIRPGTDGLFAFALIHELLKADRIDLDYLVRYANAHWLVIRNPGGADDGLFVRDESGRALCWVGGPHPGPLPRAGEGTVAERSDSTHASEDAPRHVASNTTEEPPLPPAGEGRGEGRACPADTIDISPAVVGEYTLPDGRRAVPVFHLLVERYLDPQYAPDAVSERCGIPADTIRRIARELAQAAFDNPVKLPIAWTDAHGREHSEMVGRPVSMHAMRGISAHSNGFHTCRALHLLQLLLGAVDTPGSFRYQPPFPKPLPPPNRPGKQRQANGTLDAAPLGFVHGPEDLVVDEHGQPRRIDHAFSWAYPLSAHGMMHTVIRNAWAGDPYKIDTLMMFMANMSWNSAMNTGETMHWLTDRGEDGEYRIPHIIYADAYASEMTAYADLVLPDTTYLERFDAISLLDRPISDADSACDAIRHPIVDSTTQRLHAGDEARDVRGFQSVLLDIGARLGLPGMVLDDGSPRYRDYADYIVRHERAPGVGLLAGWRGEHGELEAKGPPNPEQLQRYIDNGGFWRSHVPESARYFKMANRGYLDWAQKMGFLGHADPIVLQLYSETMQKFRLAAQGHGDKQPPAEHRERVATYFDPLPIWYEPFEGAQIADGATRFPLSAVTQRPMFMYHAWGSQNAWLRQISARNFLYLHPDTGARHGIADEDWIAVQSHHGRIQVQAKFAANVQPDTVWTWNAIGKRRGAWRLNKDAPESRKGFLLNHLISDITPKGDYANADPVTGQAAWFDLRVSIRRLDAADDTQAVSQPQFAALSFEPADDRPLRYGAQFRKNR
>NZ_CP011130.1|WP_036114820.1|5191653_5191869_-|hypothetical-protein
MELLWTLFVFAAHGGLFAVAAGSAWVGYRQRARRPGFNRWYLGAAVAAALGIAAVYVGQQLSLAMRGAITG
>NZ_CP011130.1|WP_057922694.1|5191014_5191599_+|hypothetical-protein
MIKTSLSATLTAPVLLLGLSASSLAWAGPKEEVVAAVDKFLAAKSYHAVMSMGPGPGTETDFVAPDRMRVKMGTMGEQIMIGNTLYLTMQGKTSKQAAPNGGITQLRTRDKVLGNLATLKVTAAGTENLGGVATKKYKIDNTQPKSSSTFWVNADGYPVQSVNIADVNGKQYTSTLKYSRFNDPSIKIPVPAVK
>NZ_CP011130.1|WP_036114817.1|5189956_5190925_-|YafY-family-transcriptional-regulator
MERIERIHALHRILTAARYPVTVQRLQEDLECSRATVYRDLAYLRDYLMAPVVGNGEAGFRYDTSEGDRFELPGLWLSSEELHSLLAAQQLLMRSGGGVLSNALAPLQQRIEKLLDEHAGGRRLPVERVRVIPHRTRRLDETAFRAVATAVLDRKPLTFEYRARSTDERTRRSVSPQRLTHYRENWYLDAWDHERDALRSFSVDRISAAKIGDVPARDVADEELDQHLASSYGIFSGAPKGWATIVFSAKAARWVADEHWHSQQQGRFLADGRYELKVPYSAGRELLMDVMHYGSDAEIVEPVVLREQAKSMLELALSNYGH
>NZ_CP011130.1|WP_057922693.1|5189018_5189957_-|patatin-like-phospholipase-family-protein
MPGADPPRIEKGEAVALVLGAGGARGLAQIGVIEALQARGLRIVTVAGSSSGALVGGLFAAGKMEVYRDWLFGMSRTAMLRLLDPVFGQSSLFRGERLMDSLRELAGEPRIEDLPIGFTAVAVDLMRQREVWLREGDLWDAIRASIAIPGVFTPYELHGRELVDGGLLAPLPITATRLSDAHRLVAVDMHGWPAQPPGALAHHNGGAMLATQGGGDAKPPSLFNHWFRRKASELPDEVEDDAPREMGFTELMARSLDTMQAQIARVQLALDPPELVIRIPRDACQFYEFWRARELIEIGREEAEKALDKAGY
>NZ_CP011130.1|WP_036114843.1|5199550_5200285_-|response-regulator-transcription-factor
MRVVIADDEPLARERLRALLALRPDVEIVAEAVDGQHALHACAEHRPDLVLLDIAMPGIDGLEAARHLAAFDPRPAVVFCTAYDAHALSAFDAEAIDYLVKPVRAERLDAALERVRTFAAGRERHDGGETAPGQIRSHLCARLRGSLRLIPIDDVHYLHAEEKYVIVHHARGEDLIEESLKSLEDEFGERFVRIHRNCLVARHEIVELKRNAEGHVQAVLRHGKQPLEVSRRCVAALRETLKHL
>NZ_CP011130.1|WP_082124743.1|5200305_5201292_-|histidine-kinase
MLSMAELIVIVLALAPDGTRWDLGRFVSSSAFALWLALAISVLLCVSRKWLSRLPPGVGGFIATATAAAIAAAVAGVTHTIDTVTSIGLVPAGVSFLRFVLGTAAIAILAVGVVLRYLYINDSWKAQVRANARAEVEALQARIKPHFLFNSMNTIAGLVRSDPEVAERTVLDLSDLFRAALGASKSDSSLAEEVELAERYLAIEQLRLRERLRVVWRKREPLPWKMPLPRLILQPLVENAVLHGISPLPGGGEIEIELTQLSDHLLLRIRNPSPAPAEARAGSRHAQHSIVQRLRYAYGPTARMTSGWERGYYLCELHVPTGVEAQSR
>NZ_CP011130.1|WP_046658041.1|5201388_5202090_-|alpha/beta-fold-hydrolase
METSPAASPELLDAVIRETGPTPAWSVLWLHGLGDSGDGFAPIVPELLRPDWPALRFVFPHAPVRAVTINNGMRMRAWYDIRDFSDLANRADETGVEESVRQVEALIEREIERGIPASRILLAGFSQGGAITLATALQRKQPLGGLIALSTYLPMADRLIREATAVAHTQPMFMAHGQHDPVVPYRGGEMAAARLRTLGFKIDWHAYPMAHQVCAEEIDALGDWMSQRFAAQR
>NZ_CP011130.1|WP_187313263.1|5202342_5203332_-|TonB-family-protein
MAPTGAWAGSKAASARACLWLAVCLGLAACGAAAPADAPRSQAEHADAVALPEPLVELDGEGLRARAAQALREQRIHTPAGDSAVDYYLALRDKEPGQIDVISALGELQPYVVIAGEQALLDDDLGESQRLLGLLERMDPQAPALPRLREGLRSATAARERKAREETQRLLAERADAAPAAPVSRALPGATSAAIKADAAASALAADEAAARASTPAAPIASAPAPAASPPPAPATAVASAPARAMPRLIADASPRYPLPALNRKIEGSVEISFTILPDGRTGAARLVSSEPAGVFDDAALAAVARLRFEPSGQSHAARRTLNFKLPSR
>NZ_CP011130.1|WP_148650541.1|5203674_5204091_+|hypothetical-protein
MPGLPSLAIALRYLAYGVLIAVMLIKPVLAFATEIGELAVPAAAAHEHARERPDHGNADTTDTSDAATAQTDPANDHDPDGCGDSRWHLSHCCAMQAALMPRFHIGLPLPGAAAPKPAASTSFVPSPTAVPFRPPISA
>NZ_CP011130.1|WP_057922701.1|5204219_5205542_+|TolC-family-protein
MRLRPAALAALTAALCFPAQARPPLAPTIPTETAAPQRAGSVFTLDDAFARIGDAHPDLRLFGGQRRVLEAERDGAAQRPALVGGVSVENIFGSGALSGAQGAEITLSLASVFERGGKLDARRTFAQSRIDALAVERESRRLDLLAETARRYLAVLAAQRRIELAQFDIGQRKRSVDAARVRLQAGASPESGLLTAQAAQARAELERARGERSLLAARQHLAALWGERDPGFASVAGDPYALPRIEDAAALAGLLDRNPELGRFVDARRIGEARVRLAQSQATPDLDWQVGLRRLQDGNDMALIGSVSMPLGARARAEPGIRGAQAELALLDIEREAKGLSLYSTLVEAHGRYRVGALEVARLKDDVLPRLVRAEKAAEYAYRAGAISYLELALLQAESVAVRKQRLDAALDAQLALIEIQRLTGESFLAASPIPAGATP
>NZ_CP011130.1|WP_057922702.1|5205538_5206546_+|efflux-RND-transporter-periplasmic-adaptor-subunit
MKPELMIVAGLLALSLSACGGGSDQPAAQKSAEAKQAQGEHADEASDSHEHAEGEAGHGEQSEVESTVIRTEIARRSGIGVAAVGAGTIADEHEVQGLLTPLEGRVARITARYPGPVRSLRANVGDRVSAGQTLATIDSNLSLTTYSIAAPISGVVLARNASVGEVAVEGMALFEIADLSSLWVDLHVFGEDATHLRPGLPVTVMRMGDDSGVETTLDRILPGTATASQSTVARASIKNADGLWRPGSAVRARVTVEQLPVELAVPLTALQRMDDSDVVFVREGERYSARPVKLGRRDARRVQVLSGLKAGEQVVIEQSFLIKADIEKAGASHEH
>NZ_CP011130.1|WP_057923683.1|5206598_5209823_+|CusA/CzcA-family-heavy-metal-efflux-RND-transporter
MLERILRFAIRQRWLMLALTLALIGLGVWSFGKLPIDATPDITNVQVQINTQAPGYSPLESEQRVTFPIETALAGLPKLDYTRSLSRYGLSQVTVVFKDGTDLYFARQQVAERLQQVKSQIPDGLEPELGPTATGLGEIFMYTVDADPKARKPDGSAYTATDLRTLQDWVIRPQLRNTPGVTEVNTIGGYARQIHITPDPARLRALNLTQRDLVAALAANNQNVGAGYIERNGEQFLVRVPGQIANLDAIGEIVLDRRDGVPIRVRDVASVGEGPELRSGAATQNGHEVVLGTVFMLVGSNSREVSQAAAAKLEAANASLPKGVSANAVYDRTSLVDRTIATVSKNLVEGALLVVVVLFLLLGNFRAALITAAVIPLAMLFTITGMVRGGVSGNLMSLGALDFGLIVDGAVIIIENCLRRFGEQQHLLGRQMTDDERHDLTASATAEVIRPSLFGLGIIAAVYLPIFALSGIEGKMFHPMAITVVLALTGAMLLSLTFVPAAVAIFLGGKVAEKENRAMAWIKRRYEPTLAWALRSRMIVVAGTAALVIFSGALAMRMGTEFVPSLDEGDVAVQAMRIPGTSLTQSVTMQKTMEQAFLAMTEVERVFSKIGTSEVASDPMPPSVADTFVMLKPRKQWPNPNKTKDALTEEIESIAGTLPGSNFEFTQPIQMRTNELISGVRADVAVKVYGDDLQQLLKVAQQIEAVAKQVPGAADVKTEQVTGLPMLSIEPDHRALSVYGLNPAAVQDTVATAVGGEVAGQLFEGDRRFDLVVRLPEALRQDPAALEDLPIPLPAAGADRDESSRDATWATGAPRTVPLREVATIRSVLGPNQINRENGKRRIVVTANVRDRDLGGFVGELRQRIDAQVKLPEGYWIGYGGTFEQLISASQRLAVVVPVTLVLIFALLFMAFGSAKDAAIVFSGVPLALTGGVIALALRGIPLSISAGVGFIALSGVAVLNGLVMIAFIRKLREQGDPLDNAIVDGALGRLRPVLMTALVASLGFIPMAFNVGAGSEVQRPLATVVIGGIVSSTLLTLLVLPVLYRWLHRNDAQERELESRPASDAATQASPAH
>NZ_CP011130.1|WP_057922703.1|5209949_5210846_+|cation-transporter
MGSGHDHGTTAIRHEKPLWWALGLTGGFLIAEVVGAFLTNSLALLSDAAHMGTDTLALMIALTAVRLSRKPADAKRSYGYVRMEAMGAMVNGLMLFAVAGYILWEAVGRFSQPPQVATTGMLAIASLGLAINLIAMRLLKAGSGESLNMKGAYLEVWSDMLGSVAVIAGAIVIRFTGWTVIDPILAVLIGLWVLPRTWTLLREAGNVLMEGVPKGIDLEAVRRLLTTTPGVVDVHDLHVWSLGSSTPAMTAHLVIADGVDGEALRRELSAALDERFEIEHCTLQIETTSCGEACDVSH
>NZ_CP011130.1|WP_036114855.1|5211241_5211823_-|hypothetical-protein
MRRMPIVLTVLAALSLSACGGSKVTPEQRDKAIAAFATVQKVFQHPRCQNCHIPGDQPLQFDAGIPHAMGVVRGPDGKGAAGLPCSTCHGEANLPASYGVNAPPGAPHWALPPPDHKMAWIGLPAPKLCEMIKDKRSNGGRDFAALIKHVSEDKLVLWGWEPGGERKPVSVPHPEFVEAFKTWAQADGPCPAS

Crispr_ID: NZ_CP011130_18

• CRISPR_ID: NZ_CP011130_18
• CRISPR_location: 5671709-5671774
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_18

Consensus_repeat	Method
CGCGCTGGCGTTGTCGCCGCTGGC	CRISPRCasFinder

spacers of NZ_CP011130_18

>18.1|5671733|18|NZ_CP011130|CRISPRCasFinder
GGTGTTGCCGCTGCCGAT

CRISPR arrays and Neighbor proteins around NZ_CP011130_18

CRISPR arrays

The CRISPR arrays of NZ_CP011130_18

>merge|NZ_CP011130|18|5671709-5671774|CRISPRCasFinder
GGCGAGGCTGTTGACGCCGCTGGCGGTGTTGCCGCTGCCGATCGCGGTGGCGTTGGCGCCGTCGAC

>NZ_CP011130|18|17|5671709-5671774|CRISPRCasFinder
GGCGAGGCTGTTGACGCCGCTGGC	GGTGTTGCCGCTGCCGAT
CGCGGTGGCGTTGGCGCCGTCGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224870
NZ_CP011130.1|WP_148650589.1|5655050_5655482_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224048
NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin	unknown	unknown	gnl|CDD|369347
NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease	unknown	unknown	gnl|CDD|240122
NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein	unknown	unknown	gnl|CDD|319983
NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter	unknown	unknown	gnl|CDD|226709
NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase	unknown	unknown	gnl|CDD|380163
NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein	unknown	unknown	gnl|CDD|377133
NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein	unknown	unknown	gnl|CDD|100102
NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224529
NZ_CP011130.1|WP_057923715.1|5673979_5674414_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein	unknown	unknown	gnl|CDD|226995
NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|185304
NZ_CP011130.1|WP_060410568.1|5679946_5680144_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein	unknown	unknown	gnl|CDD|181682
NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase	unknown	unknown	gnl|CDD|226712
NZ_CP011130.1|WP_036108061.1|5676238_5676487_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase	unknown	unknown	gnl|CDD|223835
NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase	unknown	unknown	gnl|CDD|275237

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator	gnl|CDD|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	3.38335e-35
NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein	gnl|CDD|100102	cd00387, Ribosomal_L7_L12, Ribosomal protein L7/L12. Ribosomal protein L7/L12 refers to the large ribosomal subunit proteins L7 and L12, which are identical except that L7 is acetylated at the N terminus. It is a component of the L7/L12 stalk, which is located at the surface of the ribosome. The stalk base consists of a portion of the 23S rRNA and ribosomal proteins L11 and L10. An extended C-terminal helix of L10 provides the binding site for L7/L12. L7/L12 consists of two domains joined by a flexible hinge, with the helical N-terminal domain (NTD) forming pairs of homodimers that bind to the extended helix of L10. It is the only multimeric ribosomal component, with either four or six copies per ribosome that occur as two or three dimers bound to the L10 helix. L7/L12 is the only ribosomal protein that does not interact directly with rRNA, but instead has indirect interactions through L10. The globular C-terminal domains of L7/L12 are highly mobile. They are exposed to the cytoplasm and contain binding sites for other molecules. Initiation factors, elongation factors, and release factors are known to interact with the L7/L12 stalk during their GTP-dependent cycles. The binding site for the factors EF-Tu and EF-G comprises L7/L12, L10, L11, the L11-binding region of 23S rRNA, and the sarcin-ricin loop of 23S rRNA. Removal of L7/L12 has minimal effect on factor binding and it has been proposed that L7/L12 induces the catalytically active conformation of EF-Tu and EF-G, thereby stimulating the GTPase activity of both factors. In eukaryotes, the proteins that perform the equivalent function to L7/L12 are called P1 and P2, which do not share sequence similarity with L7/L12. However, a bacterial L7/L12 homolog is found in some eukaryotes, in mitochondria and chloroplasts. In archaea, the protein equivalent to L7/L12 is called aL12 or L12p, but it is closer in sequence to P1 and P2 than to L7/L12.	0.00313796
NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin	gnl|CDD|369347	pfam07396, Porin_O_P, Phosphate-selective porin O and P. This family represents a conserved region approximately 400 residues long within the bacterial phosphate-selective porins O and P. These are anion-specific porins, the binding site of which has a higher affinity for phosphate than chloride ions. Porin O has a higher affinity for polyphosphates, while porin P has a higher affinity for orthophosphate. In P. aeruginosa, porin O was found to be expressed only under phosphate-starvation conditions during the stationary growth phase.	7.57116e-25
NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease	gnl|CDD|240122	cd04818, PA_subtilisin_1, PA_subtilisin_1: Protease-associated domain containing subtilisin-like proteases, subgroup 1. A subgroup of PA domain-containing subtilisin-like proteases. The significance of the PA domain to many of the proteins in which it is inserted is undetermined. It may be a protein-protein interaction domain. At peptidase active sites, the PA domain may participate in substrate binding and/or promoting conformational changes, which influence the stability and accessibility of the site to substrate. Proteins into which the PA domain is inserted include the following subtilisin-like proteases: i) melon cucumisin, ii) Arabidopsis thaliana Ara12, iii) Alnus glutinosa ag12, iv) members of the tomato P69 family, and v) tomato LeSBT2. However, these proteins belong to other subtilisin-like subgroups. Relatively little is known about proteins in this subgroup.	5.14049e-29
NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein	gnl|CDD|319983	cd16325, LolA, LolA, a periplasmic chaperone. This family contains periplasmic molecular chaperone LolA which binds to outer-membrane specific lipoproteins and transports them from inner membrane to outer membrane (OM) through LolB, a lipoprotein anchored to outer membranes. There are five Lol proteins (LolA, LolB, LolC, LolD, and LolE) involved in the sorting and membrane localization of lipoprotein and are highly conserved in Gram-negative bacteria. LolA accepts OM-specific lipoproteins that are released from the inner membrane by the LolCDE complex and transfers them to the OM receptor LolB. Studies have shown that hydrophobic surface patches large enough to accommodate acyl chains of the OM lipoproteins and the structural flexibility of LolA are important factors for its role as a periplasmic chaperone.	4.61216e-05
NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter	gnl|CDD|226709	COG4258, COG4258, Predicted exporter [General function prediction only].	0
NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase	gnl|CDD|380163	NF033113, halo_ClmS, chloramphenicol-biosynthetic FADH2-dependent halogenase CmlS.	9.61607e-51
NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein	gnl|CDD|377133	pfam03797, Autotransporter, Autotransporter beta-domain. Secretion of protein products occurs by a number of different pathways in bacteria. One of these pathways known as the type V pathway was first described for the IgA1 protease. The protein component that mediates secretion through the outer membrane is contained within the secreted protein itself, hence the proteins secreted in this way are called autotransporters. This family corresponds to the presumed integral membrane beta-barrel domain that transports the protein. This domain is found at the C-terminus of the proteins it occurs in. The N-terminus contains the variable passenger domain that is translocated across the membrane. Once the passenger domain is exported it is cleaved auto-catalytically in some proteins, in others a different protease is used and in some cases no cleavage occurs.	4.38052e-32
NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein	gnl|CDD|224529	COG1613, Sbp, ABC-type sulfate transport system, periplasmic component [Inorganic ion transport and metabolism].	0
NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein	gnl|CDD|226995	COG4648, COG4648, Predicted membrane protein [Function unknown].	1.0757e-09
NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease	gnl|CDD|185304	PRK15406, PRK15406, oligopeptide ABC transporter permease OppC; Provisional.	1.04446e-73
NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein	gnl|CDD|181682	PRK09184, PRK09184, acyl carrier protein; Provisional.	3.62542e-41
NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase	gnl|CDD|226712	COG4261, COG4261, Predicted acyltransferase [General function prediction only].	1.6131e-108
NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase	gnl|CDD|223835	COG0764, FabA, 3-hydroxymyristoyl/3-hydroxydecanoyl-(acyl carrier protein) dehydratases [Lipid metabolism].	2.49126e-14
NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase	gnl|CDD|275237	TIGR04444, hypothetical_protein_ThecoDRAFT_3161, chorismatase, FkbO/Hyg5 family. Members of this include two chemically distinct enzymes that cleave pyruvate from chorismate. FkbO and RapK convert chorismate to pyruvate plus (4R,5R)-4,5-dihydroxycyclohexa-1,5-dienecarboxylic acid (DCDC). HygB and Bra8 convert chorismate to pyruvate, water, and 3-hydroxybenzoate. These two enzymes are closely related, and lack homology to chorismate lyase, EC 4.1.3.40, which converts chorismate to pyruvate plus 4-hydroxybenzoate.	1.22848e-55

Protein sequences

>NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase
MLTGPHLQVDYLDGTPEQVLAHDDTLAVFGFGQDAPHHDDPRYLRVALEPFGDRRLERWRASGPVSSGRDGDLAWSEDGALQFGVIELDEPEPLPGEATNGEIARAAEYLYRKLIAFTAQRGYPHLLRIWNYLDGITLGHGDEERYRVFCVGRAAGLGEFPIARLPAATAIGRVDGARRLQVYWLASRTPGTPLENPRQVSAYRYPRQYGPQSPSFARAMLPPQPGAMPLLLSGTAAVVGHESKHVESVLAQLDETLTNFDSLIDAARQRWPNLPSAFGAGSCLKVYVRDVQDIDTVAAALDRRYGNRVPRILLHAAICRHELRVEIDGVHG
>NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase
MNSPASLPGTAATPVGAVASHDSKPLPDEVTQLEVDVLVVGGGPAGTTAATLLARKGWKVLLLEKGSHPRFHIGESLLPMNLAILERLGVLEQVRAIGTHKPGAEFPIDADRYNTFRFERALNPQFGYAFQVKREQFDELLFRHSQANGVDARERVKVEKVEFNDQGRPVAAVARDHDGRELRVRMRYLVDGSGRDTFIGSQLKLKQKNTLHQSAAIFSHFTGVQRRDGEDAGNITVQRFAHGWMWLIPLQGDVMSVGAVCFPEYLKQRRGETEAFLMKTLESEPSVAKRMQGAQRCGEVHVTGNYSYTCSRMTGPGWVMVGDAYAFVDPVFSSGVYLGMNSGEQAASVVDGALREPAREAELQRGMVVRLKRGLKHFQWFIYRFTTPVMRELFNAPRNFWQVEQAVISMLAGDVFDNKAVLRRLRLFRFIYAMTAVRMAPQALRGWLRRKRQVGVEFRGDTLQQGNP
>NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein
MSEQSPAERELAQLLVESLNLEDVTPEQIEPDAALFNDGLGLDSIDALELALAITKRYGFQLRSDSDENRRIFASLRALSGHIEQHRAA
>NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein
MLLAIAYPLLAHWASHEGSGVLAALALADLVVFVTIDGLLGLRALPWLATALLLGALAAIAPTPYAQMLLLTPPVLFNAWLAWWFGRSLRAPREGLITRIVAALHGCAPRELAPDLYRYTRRLTLLWACVLAGLGLVNGALAMIAVPDGVLAQLGYTPALAISQEQWSWFANILNYGVVGGMFAGEYLVRRRLFKDRPEKGFFDFLRKMAQLGPGFWKELFS
>NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase
MPFALAADHPCLPGHFPGRPLVPGVVLLDRVIEAVEALHGPLSGLRLPQVKFLRPLLPEQSAQIELDTLGAARWRFRVLHAGELLASGEIVAEPPSAPATATDEPA
>NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase
MNDSHWKQRPEGGSRFAFHLIRFIASNGGRSIARLTLYPIVTYFLIVRGPERRASRAYLARVLDRPPTLLDVARHIHTFAATILDRVYMLSRGMDRFKVNISGLEPIDRQLDRGQGMLLFGSHLGSFEALRVLARQRPDLKVRVVLDRAHNPQLTQLLDAMDPQIARNVIDAGQDGPSIVFAIKQATDEGALVALLVDRAAPGEPSTSASFLGASAQFPTAPWLIAAALKLPVVLGFGLYRGGSHYDLVFETFSEGVAIERHNRPAILAALVQRYAERLQAHARSAPYNWFNFYDFWHADDPQQALPDAGVGADVQRRVAARRSGY
>NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein
MLPSLAQPIPARTDFVEVRGSALLKAPLRVSGEYRRPDASTLVREVRAPYAETTTIRTGAQPGQGEVSIARAGKPAKKFSLSRAPELVALQTSFGALLGGDRAALEQHYRLSAQGTRRQWTITMTPKDAKLAARIREIVLLGRDDELRCIETRPARGNEQQRTLLSSAARDAAGIDDASRLAALCRGHGAAR
>NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter
MTPARRIGFALLWLALLALAGWAIGSQLKLSGDLRRFMPSAQTPAQKLLIDELGEGPGSRLLLIALEGDDPAALAAQSTALRERLSAQPQFKLVANGAGFGLESVPERLRPYRYLLSPTFDAQPLDAAYLRDQLDTRVQDLGSPAGELIEPLLASDPTLEMLRLAEAWQPAQAPQTLDGVWFDRAGKQALLAVETRAAGFDPTGQQSAIDAIRGAFEQARGTSASRITISGPGAFSVEIGGRTQREASLIGSIDSLVFIALLWLAYRSWKAPLIGGLPLATAGLAGLGAVAAIFDGVHGITVAFGFTLIGVVQDYPIHLFSHQRPGLSPWASARSLWPTLGTGVASTCIAYLTFFVSGVDGLQQLAVFTIVGLATAALATRFVLPALIDPAPRDVATSVRLARVWSALARWPRLGVTSVSLIAALALAVILFVPGAFWQNDLAKLTPVPDAALARDAQLRGELGAPDVRYIIAIEGRDAEAALQASEALLPELPLLRQRGAIAGYDLAARYLPSIKTQRERQRRLPDATNLRAALDSAVAATPFRSDAFAEFLDDVERARHAPPLTPRDLADTPLAVSVDGLLLQRGDHATALVSLSGLHDPGAVAQVVSKHGGQLLDLKQASESLVAEYRGRVLLALGLAGVLLAAAVWIALRSPRRVLRVLAPMALTTLLILAVLRGLGVELNLFHLVSLILAAGLGLDYALFFDHAGDDRAEQLRTLHAVIVCSLTTLLVFALLGLSSIPVLRAIGATVALGVAFNFVLALLIVREPTVMSDAQS
>NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein
MKLNTAILGARRVKSIAGDCRAFRSVLTLAVTMGLLTPGAASAADPINYWDNGSGVWNAGNANWTREDGSTGVWIPGVAVFRTAAAGDTVTVDGAQTFTGLEFRSNTNGYRLLGAAAGELVIGAPRAAIVVDAATQATIDATITGAGGLTVSGAGTLLLSGQGNTYGGGTTVGDSAVLAISATGALGSGSLSALDLSEIRFQGAANAGARDITLVNGFSLGRTRLRFVDQASAGNANIVIDNRVNLEDRFGVVGFEGESSAGNARISSVWGGSVNFSGRSNAGRSIIDLSQQSVLTFMDSADAGQATVVTRGAVVFRDNARADGLSLTAMGGRFGPSMQLSEMRIPLSIGSLWTENSVVLGGGSLTLGLLGRDDQVGELHGSGTVLKIGTGTLSILRDDDQYFQGTTDVKEGRLLLKTMSHGGTTVIRAAGSLIGSGGVRDLINEGTVAPDGPIRVLGNYVQRPGGRLAIDISPNGASDILSVVGNATLQGSVDVIKAPGQYAYGTRYTLIYAQGGVSGRFDMLTQNQPFLKLAMAYDAERAYLDVLRSDTQFADVCDTPNRCGVAGALDTISASGRPGADMQAVIEELTTLSVAGALAGMDRLSGDAHADFAGALLDEQSLYGQDLSRRVLAQRGDGGGRGGGGAWVRVEAASSKFGGDGNAHGWDLDTRATTLGIDGWINGSLLLGASAQFKKYDADLRPRDRGRADVGALDLYAGLHGDKGYLNAVVGYARWDNKIERGIVVGDISRHADSRYGGHRYSAYLEAGWTFDLGASRLQPLLGVSYTRLDNAGFRESGVQDVGLNGDALKVDRATAGLGLRWSADFGAGDWSVSPSLEVRALRGYGDDYVSLNATFEGAPAVGFEARGASLPKKRALADAGLQMRYGDSTELFVGYGYQHGDDLRSRNLGLGLRYRW
>NZ_CP011130.1|WP_148650589.1|5655050_5655482_+|hypothetical-protein
MNKTNFDQFLGKPLVFIESGHCCLAKLTSVSHDGNWLDAEFERNQHPSVACKYSLISTAGEKPTLNWSPPLPFQSPWAVKVSSEEFYFEEEFWQAQFLWGGGFRVFFNPRYVEEFSRGSLDWLWQHYADEEDCEDDPSDPETD
>NZ_CP011130.1|WP_057923715.1|5673979_5674414_+|hypothetical-protein
MMSTRLKVGLLMPGLLLATCCVAQAAEPSTADVSVSSSKVGIDANGKLRPLTEAESAALDKAASAQQKSAAKTSALRGKFPTNASEVRASERRLPNGAVARKMPLSQMSTLTATRDANGKIVIQHSDPSDGAAPATQQGELPRE
>NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease
MNKSLLAISIALAGAFAFAPSAQAAKLTLINGDIGTSVGLDDPTAAAPVGGNPGVSIGEQRRIVYQYAMDAWGAVLQSNVEIKVDATFARLNCTATGGTLGAAGTNWILNDFPGALPDTLYHSALADAIAGEDLVPNPLDPADITSRFNGDLGKPDCLAGSGWYLGLDGKTPEGKINFLNVVMHELGHGLGAQGFIDKTTGELLAGFTDVYTRNAYDNVQNKPFDDPTMTDALRATAMKTPGRTVWTGAQVNAQAPLVLDRRTVLNVTAPAAAAGSYEIGFADFGPAPSATSFPAGQLVLVNDGVAAASVSDGCETPFVNAADIAGKVAVIDRGTCNFAVKAKNAQLNGAVAVVIVNNTGGVAGMGNSAPPITDITIPTVMISQADGGLVKANLPATAGALVDPNFLQGADRNGRTRLYSPTVVAPGSTFSHFDTDLQPNALMEPFDTPEVQAQFDVDLTPAMFVDIGWTLNPGNAILGTCDTTVKALETPGLIIGANITAESKLCATNAHGSRALYLRCISDHATELQQIDAITTTQLGKVRQCAATVRP
>NZ_CP011130.1|WP_036108061.1|5676238_5676487_+|hypothetical-protein
MGLISLLWGIFALAWMVLALIPLLGWGNWFLIPFAAVGAIIAAIGLLFTKSENNGRAKTGLLLNAIVIVVGVVRLGIGGGII
>NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein
MNALVSLHGLRIEVDGGTSPSRRLLGPLDMELHPGQCLGVVGESGSGKSLTALALLGLLPAQLRAQGRLDIDGDDIAIASAAHARLRGRTLAWVPQDPLAALHPLRRIGAQLNETLRVVRGLSATAAGVQAQALLERVQLPDPSAALRRYPHQFSGGQRQRIAIALALATQPRVLIADEPTSALDARIARDILDLLDRLRREDGLALLLISHDLPLVGAYAQRLLVLQHGEVVERGDTATVFASPAHAYTRELLAADRIDALPPESAAQADNDTPPLLRGEALSMRYPRAPRPALDGVDIELRRGQGLALVGESGSGKSTLGRVLLRLLRGAQGRVSIDGIDLGSLDAAALRRLRARTGVVFQDPYASLDPRLRVAEIVAEPLRIHGNLDKAARRARAAELLRDVGLDEAMLDRYPHQFSGGQRQRIAIARALATSPDLLVCDEAVSALDAHHRAAILALLARLKRERGLALLFVTHDLAAAAAVAERIAVLEAGRIVETGPTAQVLSTPRHAHTRALLAARPAVIGSV
>NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease
MRSFMSLPPLARTCLLVLAALAALCWLAPMLGRYGAILPDWDALSARPGTARHWFGTDAIGRDVFARTLAGGRLSLGIGLLASVVALVIGLGYGAIAGLAGGWVERLMVRVLDVFSALPFLLVVILLLTLFERSLLLLLAAIGGYVWIDLARVMRAEAARLREAPFVLAAQAAGASFGQRLRWHVLPNLMPLAFVYLGLILPQAILVESFLGFLGLSIDEPSSSWGGLLAEGVQELDSAPWTLLFPAGFLVTTLAAFQFLGDGLRDWLDVHRSPQGDAPRQAAVA
>NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator
MLTMKAKYALRAMCALARAEHARRPTDPAQVPRPRRERLQARTIAEHSGAPGKFLETILVDLRQAGFIDSRRGQKGGHALARPADQIMVGDLIRAIDGPLAPVRCASVSAYQACADCPDPDACSLRSLMREARDAISDVLDRRSLRELALAPDFLAALPIAEASLNLDGGLS
>NZ_CP011130.1|WP_060410568.1|5679946_5680144_+|hypothetical-protein
MRYPIARDPEPEINIVNLSDTEYVLLNAVRELRAGRIEVVIQGSRIVEITRTQRVEVDAAQESWA
>NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin
MQTRVRPALNARTATVSLWSALACALALPVHAQSNELTVEQLAQRLRAIEQRLGGGEAVANASADSGNLSDLDQRLRVIERKLELQAEENAARVASTPVVSLSASKGLSVKSPPPGDVELKFKALVQADGRFFIDDRQLPQNDTFLFRRIMPTIEGTWGPLIGFRLTPEFAGDSATIADAYFDLKFDPRATVRIGKFKSPVGLERLQSSGSTGLIELGLASELTPNRDLGVQLQGELAGSTVSYALGVFNGAVDGRDSPTVNPDNEFELAGRVFVEPWKNASNALSGLGFGLAASSGDRRGNGNNFLPRYRTPGQTQFFNYRSAVLADGAQTRWSPQAFYYRNGLSLLGEYVSSSQDVRVGAFADELEHTAWQLTAGYVLTGEDAGYKGVARPNQPFTLGAAGWGAFELVARYGRLEIDDDAFPRYADRNAVAAAARSWGLGLNWYLTGNLKLVANYTQTQFDGGAAAGRDREDEKAFFTRAQLAF
>NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein
MKTALRLTLLALALAAAGTVSAKDTDLLNVSYDPTREFYAEVNQVFAAQWKQQTGETLNIRASHGGSGKQARAVVDGLEADVVTLALAGDIDTIANAKQLPANWQSRLPHQSSPYTSTIVFLVRKGNPKGIKDWDDLIKPGVAVITPNPKTSGGARWNYLAAWAYASTKFRDGDKVVDFLTSLFKNVPVLDTGARGSTTTFVDRKIGDVLIAWENEALLTLEQANTRGQFEVVIPSLSIKAEPPVAWVDKNVDKHGTRKQAEAYLRFLYTPEGQRLAAKHGYRPAEPDKVPAAELAKFPQVKQVTIDGAFGGWKKAQAAHFSDGGFFDKIYLPK
>NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein
MNRVIILGWVPGFNKIEANKQLRTYLGYDLREAKDMVDAIVRGDAVEFFLPADKSVEICMQLERIGALCRQVPSEDNS

Crispr_ID: NZ_CP011130_17

• CRISPR_ID: NZ_CP011130_17
• CRISPR_location: 5671049-5671451
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 7 spacers

Consensus repeat of NZ_CP011130_17

Consensus_repeat	Method
CGCGCTGGCGTTGTCGCCGCTGGC	CRISPRCasFinder

spacers of NZ_CP011130_17

>17.1|5671073|18|NZ_CP011130|CRISPRCasFinder
GGTGTTGCCGCTGCCGAT
>17.2|5671115|18|NZ_CP011130|CRISPRCasFinder
TACGTTGGCGTTGCCGAA
>17.3|5671157|60|NZ_CP011130|CRISPRCasFinder
CTGGTTGGTCGAGCCGAACGCATTGCTGCCCGCGCCCAAAACCGTATTGAAGTTGCCGAA
>17.4|5671241|18|NZ_CP011130|CRISPRCasFinder
CTGATTGACGTAACCGAA
>17.5|5671283|60|NZ_CP011130|CRISPRCasFinder
ACCGTTCAAGGTACCGAACGCCGCGCTTTCCAAGCCGCTGGCGGTATTGCCCCAACCCAC
>17.6|5671367|18|NZ_CP011130|CRISPRCasFinder
GATGCTGGAGTTGCCCAC
>17.7|5671409|18|NZ_CP011130|CRISPRCasFinder
GAGGCTGCCGTTGCCGAG

CRISPR arrays and Neighbor proteins around NZ_CP011130_17

CRISPR arrays

The CRISPR arrays of NZ_CP011130_17

>merge|NZ_CP011130|17|5671049-5671451|CRISPRCasFinder
CGCGAAGCTGTTGGCGCCGCTGGCGGTGTTGCCGCTGCCGATCGCGGTCGCGTTGGCGCCGTCGACTACGTTGGCGTTGCCGAAGGCGCTGGCGTTGTCCGAGTTCACCTGGTTGGTCGAGCCGAACGCATTGCTGCCCGCGCCCAAAACCGTATTGAAGTTGCCGAACGCGCTGCTGTTCTCGCCGACGGCCTGATTGACGTAACCGAACGCGCTGGAGTAATCGCCCTCCGCACCGTTCAAGGTACCGAACGCCGCGCTTTCCAAGCCGCTGGCGGTATTGCCCCAACCCACCGCGCTGGCGTTGTCGCCGCTGGCGATGCTGGAGTTGCCCACCGCGGTGCTGTTCGCGCCGCTGGCGAGGCTGCCGTTGCCGAGCGCGCTGGCGTTGTCGCCGCTGGCC

>NZ_CP011130|17|16|5671049-5671451|CRISPRCasFinder
CGCGAAGCTGTTGGCGCCGCTGGC	GGTGTTGCCGCTGCCGAT
CGCGGTCGCGTTGGCGCCGTCGAC	TACGTTGGCGTTGCCGAA
GGCGCTGGCGTTGTCCGAGTTCAC	CTGGTTGGTCGAGCCGAACGCATTGCTGCCCGCGCCCAAAACCGTATTGAAGTTGCCGAA
CGCGCTGCTGTTCTCGCCGACGGC	CTGATTGACGTAACCGAA
CGCGCTGGAGTAATCGCCCTCCGC	ACCGTTCAAGGTACCGAACGCCGCGCTTTCCAAGCCGCTGGCGGTATTGCCCCAACCCAC
CGCGCTGGCGTTGTCGCCGCTGGC	GATGCTGGAGTTGCCCAC
CGCGGTGCTGTTCGCGCCGCTGGC	GAGGCTGCCGTTGCCGAG
CGCGCTGGCGTTGTCGCCGCTGGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224870
NZ_CP011130.1|WP_148650589.1|5655050_5655482_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224048
NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin	unknown	unknown	gnl|CDD|369347
NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease	unknown	unknown	gnl|CDD|240122
NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein	unknown	unknown	gnl|CDD|319983
NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter	unknown	unknown	gnl|CDD|226709
NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase	unknown	unknown	gnl|CDD|380163
NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein	unknown	unknown	gnl|CDD|377133
NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein	unknown	unknown	gnl|CDD|100102
NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224529
NZ_CP011130.1|WP_057923715.1|5673979_5674414_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein	unknown	unknown	gnl|CDD|226995
NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|185304
NZ_CP011130.1|WP_060410568.1|5679946_5680144_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein	unknown	unknown	gnl|CDD|181682
NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase	unknown	unknown	gnl|CDD|226712
NZ_CP011130.1|WP_036108061.1|5676238_5676487_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase	unknown	unknown	gnl|CDD|223835
NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase	unknown	unknown	gnl|CDD|275237

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator	gnl|CDD|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	3.38335e-35
NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein	gnl|CDD|100102	cd00387, Ribosomal_L7_L12, Ribosomal protein L7/L12. Ribosomal protein L7/L12 refers to the large ribosomal subunit proteins L7 and L12, which are identical except that L7 is acetylated at the N terminus. It is a component of the L7/L12 stalk, which is located at the surface of the ribosome. The stalk base consists of a portion of the 23S rRNA and ribosomal proteins L11 and L10. An extended C-terminal helix of L10 provides the binding site for L7/L12. L7/L12 consists of two domains joined by a flexible hinge, with the helical N-terminal domain (NTD) forming pairs of homodimers that bind to the extended helix of L10. It is the only multimeric ribosomal component, with either four or six copies per ribosome that occur as two or three dimers bound to the L10 helix. L7/L12 is the only ribosomal protein that does not interact directly with rRNA, but instead has indirect interactions through L10. The globular C-terminal domains of L7/L12 are highly mobile. They are exposed to the cytoplasm and contain binding sites for other molecules. Initiation factors, elongation factors, and release factors are known to interact with the L7/L12 stalk during their GTP-dependent cycles. The binding site for the factors EF-Tu and EF-G comprises L7/L12, L10, L11, the L11-binding region of 23S rRNA, and the sarcin-ricin loop of 23S rRNA. Removal of L7/L12 has minimal effect on factor binding and it has been proposed that L7/L12 induces the catalytically active conformation of EF-Tu and EF-G, thereby stimulating the GTPase activity of both factors. In eukaryotes, the proteins that perform the equivalent function to L7/L12 are called P1 and P2, which do not share sequence similarity with L7/L12. However, a bacterial L7/L12 homolog is found in some eukaryotes, in mitochondria and chloroplasts. In archaea, the protein equivalent to L7/L12 is called aL12 or L12p, but it is closer in sequence to P1 and P2 than to L7/L12.	0.00313796
NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin	gnl|CDD|369347	pfam07396, Porin_O_P, Phosphate-selective porin O and P. This family represents a conserved region approximately 400 residues long within the bacterial phosphate-selective porins O and P. These are anion-specific porins, the binding site of which has a higher affinity for phosphate than chloride ions. Porin O has a higher affinity for polyphosphates, while porin P has a higher affinity for orthophosphate. In P. aeruginosa, porin O was found to be expressed only under phosphate-starvation conditions during the stationary growth phase.	7.57116e-25
NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease	gnl|CDD|240122	cd04818, PA_subtilisin_1, PA_subtilisin_1: Protease-associated domain containing subtilisin-like proteases, subgroup 1. A subgroup of PA domain-containing subtilisin-like proteases. The significance of the PA domain to many of the proteins in which it is inserted is undetermined. It may be a protein-protein interaction domain. At peptidase active sites, the PA domain may participate in substrate binding and/or promoting conformational changes, which influence the stability and accessibility of the site to substrate. Proteins into which the PA domain is inserted include the following subtilisin-like proteases: i) melon cucumisin, ii) Arabidopsis thaliana Ara12, iii) Alnus glutinosa ag12, iv) members of the tomato P69 family, and v) tomato LeSBT2. However, these proteins belong to other subtilisin-like subgroups. Relatively little is known about proteins in this subgroup.	5.14049e-29
NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein	gnl|CDD|319983	cd16325, LolA, LolA, a periplasmic chaperone. This family contains periplasmic molecular chaperone LolA which binds to outer-membrane specific lipoproteins and transports them from inner membrane to outer membrane (OM) through LolB, a lipoprotein anchored to outer membranes. There are five Lol proteins (LolA, LolB, LolC, LolD, and LolE) involved in the sorting and membrane localization of lipoprotein and are highly conserved in Gram-negative bacteria. LolA accepts OM-specific lipoproteins that are released from the inner membrane by the LolCDE complex and transfers them to the OM receptor LolB. Studies have shown that hydrophobic surface patches large enough to accommodate acyl chains of the OM lipoproteins and the structural flexibility of LolA are important factors for its role as a periplasmic chaperone.	4.61216e-05
NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter	gnl|CDD|226709	COG4258, COG4258, Predicted exporter [General function prediction only].	0
NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase	gnl|CDD|380163	NF033113, halo_ClmS, chloramphenicol-biosynthetic FADH2-dependent halogenase CmlS.	9.61607e-51
NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein	gnl|CDD|377133	pfam03797, Autotransporter, Autotransporter beta-domain. Secretion of protein products occurs by a number of different pathways in bacteria. One of these pathways known as the type V pathway was first described for the IgA1 protease. The protein component that mediates secretion through the outer membrane is contained within the secreted protein itself, hence the proteins secreted in this way are called autotransporters. This family corresponds to the presumed integral membrane beta-barrel domain that transports the protein. This domain is found at the C-terminus of the proteins it occurs in. The N-terminus contains the variable passenger domain that is translocated across the membrane. Once the passenger domain is exported it is cleaved auto-catalytically in some proteins, in others a different protease is used and in some cases no cleavage occurs.	4.38052e-32
NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein	gnl|CDD|224529	COG1613, Sbp, ABC-type sulfate transport system, periplasmic component [Inorganic ion transport and metabolism].	0
NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein	gnl|CDD|226995	COG4648, COG4648, Predicted membrane protein [Function unknown].	1.0757e-09
NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease	gnl|CDD|185304	PRK15406, PRK15406, oligopeptide ABC transporter permease OppC; Provisional.	1.04446e-73
NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein	gnl|CDD|181682	PRK09184, PRK09184, acyl carrier protein; Provisional.	3.62542e-41
NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase	gnl|CDD|226712	COG4261, COG4261, Predicted acyltransferase [General function prediction only].	1.6131e-108
NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase	gnl|CDD|223835	COG0764, FabA, 3-hydroxymyristoyl/3-hydroxydecanoyl-(acyl carrier protein) dehydratases [Lipid metabolism].	2.49126e-14
NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase	gnl|CDD|275237	TIGR04444, hypothetical_protein_ThecoDRAFT_3161, chorismatase, FkbO/Hyg5 family. Members of this include two chemically distinct enzymes that cleave pyruvate from chorismate. FkbO and RapK convert chorismate to pyruvate plus (4R,5R)-4,5-dihydroxycyclohexa-1,5-dienecarboxylic acid (DCDC). HygB and Bra8 convert chorismate to pyruvate, water, and 3-hydroxybenzoate. These two enzymes are closely related, and lack homology to chorismate lyase, EC 4.1.3.40, which converts chorismate to pyruvate plus 4-hydroxybenzoate.	1.22848e-55

Protein sequences

>NZ_CP011130.1|WP_046659518.1|5666434_5667433_+|pteridine-dependent-deoxygenase
MLTGPHLQVDYLDGTPEQVLAHDDTLAVFGFGQDAPHHDDPRYLRVALEPFGDRRLERWRASGPVSSGRDGDLAWSEDGALQFGVIELDEPEPLPGEATNGEIARAAEYLYRKLIAFTAQRGYPHLLRIWNYLDGITLGHGDEERYRVFCVGRAAGLGEFPIARLPAATAIGRVDGARRLQVYWLASRTPGTPLENPRQVSAYRYPRQYGPQSPSFARAMLPPQPGAMPLLLSGTAAVVGHESKHVESVLAQLDETLTNFDSLIDAARQRWPNLPSAFGAGSCLKVYVRDVQDIDTVAAALDRRYGNRVPRILLHAAICRHELRVEIDGVHG
>NZ_CP011130.1|WP_082648753.1|5665013_5666420_+|tryptophan-7-halogenase
MNSPASLPGTAATPVGAVASHDSKPLPDEVTQLEVDVLVVGGGPAGTTAATLLARKGWKVLLLEKGSHPRFHIGESLLPMNLAILERLGVLEQVRAIGTHKPGAEFPIDADRYNTFRFERALNPQFGYAFQVKREQFDELLFRHSQANGVDARERVKVEKVEFNDQGRPVAAVARDHDGRELRVRMRYLVDGSGRDTFIGSQLKLKQKNTLHQSAAIFSHFTGVQRRDGEDAGNITVQRFAHGWMWLIPLQGDVMSVGAVCFPEYLKQRRGETEAFLMKTLESEPSVAKRMQGAQRCGEVHVTGNYSYTCSRMTGPGWVMVGDAYAFVDPVFSSGVYLGMNSGEQAASVVDGALREPAREAELQRGMVVRLKRGLKHFQWFIYRFTTPVMRELFNAPRNFWQVEQAVISMLAGDVFDNKAVLRRLRLFRFIYAMTAVRMAPQALRGWLRRKRQVGVEFRGDTLQQGNP
>NZ_CP011130.1|WP_036108074.1|5664524_5664794_-|acyl-carrier-protein
MSEQSPAERELAQLLVESLNLEDVTPEQIEPDAALFNDGLGLDSIDALELALAITKRYGFQLRSDSDENRRIFASLRALSGHIEQHRAA
>NZ_CP011130.1|WP_057923713.1|5663558_5664227_-|hypothetical-protein
MLLAIAYPLLAHWASHEGSGVLAALALADLVVFVTIDGLLGLRALPWLATALLLGALAAIAPTPYAQMLLLTPPVLFNAWLAWWFGRSLRAPREGLITRIVAALHGCAPRELAPDLYRYTRRLTLLWACVLAGLGLVNGALAMIAVPDGVLAQLGYTPALAISQEQWSWFANILNYGVVGGMFAGEYLVRRRLFKDRPEKGFFDFLRKMAQLGPGFWKELFS
>NZ_CP011130.1|WP_057922934.1|5662958_5663279_-|dehydratase
MPFALAADHPCLPGHFPGRPLVPGVVLLDRVIEAVEALHGPLSGLRLPQVKFLRPLLPEQSAQIELDTLGAARWRFRVLHAGELLASGEIVAEPPSAPATATDEPA
>NZ_CP011130.1|WP_057922933.1|5661981_5662962_-|acyltransferase
MNDSHWKQRPEGGSRFAFHLIRFIASNGGRSIARLTLYPIVTYFLIVRGPERRASRAYLARVLDRPPTLLDVARHIHTFAATILDRVYMLSRGMDRFKVNISGLEPIDRQLDRGQGMLLFGSHLGSFEALRVLARQRPDLKVRVVLDRAHNPQLTQLLDAMDPQIARNVIDAGQDGPSIVFAIKQATDEGALVALLVDRAAPGEPSTSASFLGASAQFPTAPWLIAAALKLPVVLGFGLYRGGSHYDLVFETFSEGVAIERHNRPAILAALVQRYAERLQAHARSAPYNWFNFYDFWHADDPQQALPDAGVGADVQRRVAARRSGY
>NZ_CP011130.1|WP_046659517.1|5661335_5661914_-|hypothetical-protein
MLPSLAQPIPARTDFVEVRGSALLKAPLRVSGEYRRPDASTLVREVRAPYAETTTIRTGAQPGQGEVSIARAGKPAKKFSLSRAPELVALQTSFGALLGGDRAALEQHYRLSAQGTRRQWTITMTPKDAKLAARIREIVLLGRDDELRCIETRPARGNEQQRTLLSSAARDAAGIDDASRLAALCRGHGAAR
>NZ_CP011130.1|WP_057923712.1|5658999_5661336_-|MMPL-family-transporter
MTPARRIGFALLWLALLALAGWAIGSQLKLSGDLRRFMPSAQTPAQKLLIDELGEGPGSRLLLIALEGDDPAALAAQSTALRERLSAQPQFKLVANGAGFGLESVPERLRPYRYLLSPTFDAQPLDAAYLRDQLDTRVQDLGSPAGELIEPLLASDPTLEMLRLAEAWQPAQAPQTLDGVWFDRAGKQALLAVETRAAGFDPTGQQSAIDAIRGAFEQARGTSASRITISGPGAFSVEIGGRTQREASLIGSIDSLVFIALLWLAYRSWKAPLIGGLPLATAGLAGLGAVAAIFDGVHGITVAFGFTLIGVVQDYPIHLFSHQRPGLSPWASARSLWPTLGTGVASTCIAYLTFFVSGVDGLQQLAVFTIVGLATAALATRFVLPALIDPAPRDVATSVRLARVWSALARWPRLGVTSVSLIAALALAVILFVPGAFWQNDLAKLTPVPDAALARDAQLRGELGAPDVRYIIAIEGRDAEAALQASEALLPELPLLRQRGAIAGYDLAARYLPSIKTQRERQRRLPDATNLRAALDSAVAATPFRSDAFAEFLDDVERARHAPPLTPRDLADTPLAVSVDGLLLQRGDHATALVSLSGLHDPGAVAQVVSKHGGQLLDLKQASESLVAEYRGRVLLALGLAGVLLAAAVWIALRSPRRVLRVLAPMALTTLLILAVLRGLGVELNLFHLVSLILAAGLGLDYALFFDHAGDDRAEQLRTLHAVIVCSLTTLLVFALLGLSSIPVLRAIGATVALGVAFNFVLALLIVREPTVMSDAQS
>NZ_CP011130.1|WP_082648752.1|5656077_5658831_-|autotransporter-domain-containing-protein
MKLNTAILGARRVKSIAGDCRAFRSVLTLAVTMGLLTPGAASAADPINYWDNGSGVWNAGNANWTREDGSTGVWIPGVAVFRTAAAGDTVTVDGAQTFTGLEFRSNTNGYRLLGAAAGELVIGAPRAAIVVDAATQATIDATITGAGGLTVSGAGTLLLSGQGNTYGGGTTVGDSAVLAISATGALGSGSLSALDLSEIRFQGAANAGARDITLVNGFSLGRTRLRFVDQASAGNANIVIDNRVNLEDRFGVVGFEGESSAGNARISSVWGGSVNFSGRSNAGRSIIDLSQQSVLTFMDSADAGQATVVTRGAVVFRDNARADGLSLTAMGGRFGPSMQLSEMRIPLSIGSLWTENSVVLGGGSLTLGLLGRDDQVGELHGSGTVLKIGTGTLSILRDDDQYFQGTTDVKEGRLLLKTMSHGGTTVIRAAGSLIGSGGVRDLINEGTVAPDGPIRVLGNYVQRPGGRLAIDISPNGASDILSVVGNATLQGSVDVIKAPGQYAYGTRYTLIYAQGGVSGRFDMLTQNQPFLKLAMAYDAERAYLDVLRSDTQFADVCDTPNRCGVAGALDTISASGRPGADMQAVIEELTTLSVAGALAGMDRLSGDAHADFAGALLDEQSLYGQDLSRRVLAQRGDGGGRGGGGAWVRVEAASSKFGGDGNAHGWDLDTRATTLGIDGWINGSLLLGASAQFKKYDADLRPRDRGRADVGALDLYAGLHGDKGYLNAVVGYARWDNKIERGIVVGDISRHADSRYGGHRYSAYLEAGWTFDLGASRLQPLLGVSYTRLDNAGFRESGVQDVGLNGDALKVDRATAGLGLRWSADFGAGDWSVSPSLEVRALRGYGDDYVSLNATFEGAPAVGFEARGASLPKKRALADAGLQMRYGDSTELFVGYGYQHGDDLRSRNLGLGLRYRW
>NZ_CP011130.1|WP_148650589.1|5655050_5655482_+|hypothetical-protein
MNKTNFDQFLGKPLVFIESGHCCLAKLTSVSHDGNWLDAEFERNQHPSVACKYSLISTAGEKPTLNWSPPLPFQSPWAVKVSSEEFYFEEEFWQAQFLWGGGFRVFFNPRYVEEFSRGSLDWLWQHYADEEDCEDDPSDPETD
>NZ_CP011130.1|WP_057923715.1|5673979_5674414_+|hypothetical-protein
MMSTRLKVGLLMPGLLLATCCVAQAAEPSTADVSVSSSKVGIDANGKLRPLTEAESAALDKAASAQQKSAAKTSALRGKFPTNASEVRASERRLPNGAVARKMPLSQMSTLTATRDANGKIVIQHSDPSDGAAPATQQGELPRE
>NZ_CP011130.1|WP_057922936.1|5674406_5676062_+|serine-protease
MNKSLLAISIALAGAFAFAPSAQAAKLTLINGDIGTSVGLDDPTAAAPVGGNPGVSIGEQRRIVYQYAMDAWGAVLQSNVEIKVDATFARLNCTATGGTLGAAGTNWILNDFPGALPDTLYHSALADAIAGEDLVPNPLDPADITSRFNGDLGKPDCLAGSGWYLGLDGKTPEGKINFLNVVMHELGHGLGAQGFIDKTTGELLAGFTDVYTRNAYDNVQNKPFDDPTMTDALRATAMKTPGRTVWTGAQVNAQAPLVLDRRTVLNVTAPAAAAGSYEIGFADFGPAPSATSFPAGQLVLVNDGVAAASVSDGCETPFVNAADIAGKVAVIDRGTCNFAVKAKNAQLNGAVAVVIVNNTGGVAGMGNSAPPITDITIPTVMISQADGGLVKANLPATAGALVDPNFLQGADRNGRTRLYSPTVVAPGSTFSHFDTDLQPNALMEPFDTPEVQAQFDVDLTPAMFVDIGWTLNPGNAILGTCDTTVKALETPGLIIGANITAESKLCATNAHGSRALYLRCISDHATELQQIDAITTTQLGKVRQCAATVRP
>NZ_CP011130.1|WP_036108061.1|5676238_5676487_+|hypothetical-protein
MGLISLLWGIFALAWMVLALIPLLGWGNWFLIPFAAVGAIIAAIGLLFTKSENNGRAKTGLLLNAIVIVVGVVRLGIGGGII
>NZ_CP011130.1|WP_057922937.1|5676615_5678205_-|ABC-transporter-ATP-binding-protein
MNALVSLHGLRIEVDGGTSPSRRLLGPLDMELHPGQCLGVVGESGSGKSLTALALLGLLPAQLRAQGRLDIDGDDIAIASAAHARLRGRTLAWVPQDPLAALHPLRRIGAQLNETLRVVRGLSATAAGVQAQALLERVQLPDPSAALRRYPHQFSGGQRQRIAIALALATQPRVLIADEPTSALDARIARDILDLLDRLRREDGLALLLISHDLPLVGAYAQRLLVLQHGEVVERGDTATVFASPAHAYTRELLAADRIDALPPESAAQADNDTPPLLRGEALSMRYPRAPRPALDGVDIELRRGQGLALVGESGSGKSTLGRVLLRLLRGAQGRVSIDGIDLGSLDAAALRRLRARTGVVFQDPYASLDPRLRVAEIVAEPLRIHGNLDKAARRARAAELLRDVGLDEAMLDRYPHQFSGGQRQRIAIARALATSPDLLVCDEAVSALDAHHRAAILALLARLKRERGLALLFVTHDLAAAAAVAERIAVLEAGRIVETGPTAQVLSTPRHAHTRALLAARPAVIGSV
>NZ_CP011130.1|WP_057922938.1|5678201_5679059_-|ABC-transporter-permease
MRSFMSLPPLARTCLLVLAALAALCWLAPMLGRYGAILPDWDALSARPGTARHWFGTDAIGRDVFARTLAGGRLSLGIGLLASVVALVIGLGYGAIAGLAGGWVERLMVRVLDVFSALPFLLVVILLLTLFERSLLLLLAAIGGYVWIDLARVMRAEAARLREAPFVLAAQAAGASFGQRLRWHVLPNLMPLAFVYLGLILPQAILVESFLGFLGLSIDEPSSSWGGLLAEGVQELDSAPWTLLFPAGFLVTTLAAFQFLGDGLRDWLDVHRSPQGDAPRQAAVA
>NZ_CP011130.1|WP_082648754.1|5679299_5679818_+|Rrf2-family-transcriptional-regulator
MLTMKAKYALRAMCALARAEHARRPTDPAQVPRPRRERLQARTIAEHSGAPGKFLETILVDLRQAGFIDSRRGQKGGHALARPADQIMVGDLIRAIDGPLAPVRCASVSAYQACADCPDPDACSLRSLMREARDAISDVLDRRSLRELALAPDFLAALPIAEASLNLDGGLS
>NZ_CP011130.1|WP_060410568.1|5679946_5680144_+|hypothetical-protein
MRYPIARDPEPEINIVNLSDTEYVLLNAVRELRAGRIEVVIQGSRIVEITRTQRVEVDAAQESWA
>NZ_CP011130.1|WP_057922940.1|5680315_5681776_+|porin
MQTRVRPALNARTATVSLWSALACALALPVHAQSNELTVEQLAQRLRAIEQRLGGGEAVANASADSGNLSDLDQRLRVIERKLELQAEENAARVASTPVVSLSASKGLSVKSPPPGDVELKFKALVQADGRFFIDDRQLPQNDTFLFRRIMPTIEGTWGPLIGFRLTPEFAGDSATIADAYFDLKFDPRATVRIGKFKSPVGLERLQSSGSTGLIELGLASELTPNRDLGVQLQGELAGSTVSYALGVFNGAVDGRDSPTVNPDNEFELAGRVFVEPWKNASNALSGLGFGLAASSGDRRGNGNNFLPRYRTPGQTQFFNYRSAVLADGAQTRWSPQAFYYRNGLSLLGEYVSSSQDVRVGAFADELEHTAWQLTAGYVLTGEDAGYKGVARPNQPFTLGAAGWGAFELVARYGRLEIDDDAFPRYADRNAVAAAARSWGLGLNWYLTGNLKLVANYTQTQFDGGAAAGRDREDEKAFFTRAQLAF
>NZ_CP011130.1|WP_057922941.1|5681809_5682814_+|sulfate-ABC-transporter-substrate-binding-protein
MKTALRLTLLALALAAAGTVSAKDTDLLNVSYDPTREFYAEVNQVFAAQWKQQTGETLNIRASHGGSGKQARAVVDGLEADVVTLALAGDIDTIANAKQLPANWQSRLPHQSSPYTSTIVFLVRKGNPKGIKDWDDLIKPGVAVITPNPKTSGGARWNYLAAWAYASTKFRDGDKVVDFLTSLFKNVPVLDTGARGSTTTFVDRKIGDVLIAWENEALLTLEQANTRGQFEVVIPSLSIKAEPPVAWVDKNVDKHGTRKQAEAYLRFLYTPEGQRLAAKHGYRPAEPDKVPAAELAKFPQVKQVTIDGAFGGWKKAQAAHFSDGGFFDKIYLPK
>NZ_CP011130.1|WP_082648755.1|5683091_5683328_-|hypothetical-protein
MNRVIILGWVPGFNKIEANKQLRTYLGYDLREAKDMVDAIVRGDAVEFFLPADKSVEICMQLERIGALCRQVPSEDNS

Crispr_ID: NZ_CP011130_19

• CRISPR_ID: NZ_CP011130_19
• CRISPR_location: 5712391-5712492
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_19

Consensus_repeat	Method
CGCCGAAGTAAAGCAGAGCCCGC	CRISPRCasFinder

spacers of NZ_CP011130_19

>19.1|5712414|56|NZ_CP011130|CRISPRCasFinder
CTTCGCGGGAATGACGTTCTAGAGAGATGGCGCTGAAGGCTTTGGATGTCCGGCTT

CRISPR arrays and Neighbor proteins around NZ_CP011130_19

CRISPR arrays

The CRISPR arrays of NZ_CP011130_19

>merge|NZ_CP011130|19|5712391-5712492|CRISPRCasFinder
CGCCGAAGTAAAGCAGAGCCCGCCTTCGCGGGAATGACGTTCTAGAGAGATGGCGCTGAAGGCTTTGGATGTCCGGCTTCGCCGAAGCAAAGCAGAGCCCGC

>NZ_CP011130|19|18|5712391-5712492|CRISPRCasFinder
CGCCGAAGTAAAGCAGAGCCCGC	CTTCGCGGGAATGACGTTCTAGAGAGATGGCGCTGAAGGCTTTGGATGTCCGGCTT
CGCCGAAGCAAAGCAGAGCCCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_036107968.1|5718618_5719050_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036107986.1|5712604_5712880_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl|CDD|225170
NZ_CP011130.1|WP_057922956.1|5716499_5717318_+|ParA-family-protein	unknown	unknown	gnl|CDD|379293
NZ_CP011130.1|WP_057922957.1|5719352_5720318_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187563
NZ_CP011130.1|WP_036108007.1|5703834_5704848_-|stage-II-sporulation-protein-M	unknown	unknown	gnl|CDD|376676
NZ_CP011130.1|WP_057922953.1|5708866_5710129_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922949.1|5700980_5702195_-|DUF4350-domain-containing-protein	unknown	unknown	gnl|CDD|379527
NZ_CP011130.1|WP_082124568.1|5714833_5715457_+|4'-phosphopantetheinyl-transferase-superfamily-protein	unknown	unknown	gnl|CDD|225002
NZ_CP011130.1|WP_082648760.1|5713214_5714615_-|acyl-CoA-synthetase	unknown	unknown	gnl|CDD|223442
NZ_CP011130.1|WP_036107988.1|5711401_5712172_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197320
NZ_CP011130.1|WP_036107957.1|5721379_5721715_+|lipid-A-disaccharide-synthase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|226461
NZ_CP011130.1|WP_057922954.1|5710125_5711373_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922951.1|5705527_5706040_-|RDD-family-protein	unknown	unknown	gnl|CDD|377640
NZ_CP011130.1|WP_036108004.1|5704844_5705528_-|RDD-family-protein	unknown	unknown	gnl|CDD|377640
NZ_CP011130.1|WP_057922958.1|5720643_5721369_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133022
NZ_CP011130.1|WP_036107971.1|5717314_5718232_+|ParB/RepB/Spo0J-family-partition-protein	unknown	unknown	gnl|CDD|275105
NZ_CP011130.1|WP_057922950.1|5702191_5703838_-|DUF4129-domain-containing-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057922952.1|5706936_5708364_+|coniferyl-aldehyde-dehydrogenase	unknown	unknown	gnl|CDD|143451
NZ_CP011130.1|WP_057922955.1|5715644_5716310_+|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG	unknown	unknown	gnl|CDD|234637
NZ_CP011130.1|WP_036108115.1|5706107_5706650_-|gamma-carbonic-anhydrase-family-protein	unknown	unknown	gnl|CDD|100051

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_036107986.1|5712604_5712880_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl|CDD|225170	COG2261, COG2261, Predicted membrane protein [Function unknown].	2.02983e-10
NZ_CP011130.1|WP_057922956.1|5716499_5717318_+|ParA-family-protein	gnl|CDD|379293	pfam13614, AAA_31, AAA domain. This family includes a wide variety of AAA domains including some that have lost essential nucleotide binding residues in the P-loop.	4.24036e-92
NZ_CP011130.1|WP_057922957.1|5719352_5720318_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187563	cd05253, UDP_GE_SDE_e, UDP glucuronic acid epimerase, extended (e) SDRs. This subgroup contains UDP-D-glucuronic acid 4-epimerase, an extended SDR, which catalyzes the conversion of UDP-alpha-D-glucuronic acid to UDP-alpha-D-galacturonic acid. This group has the SDR's canonical catalytic tetrad and the TGxxGxxG NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	3.40476e-179
NZ_CP011130.1|WP_036108007.1|5703834_5704848_-|stage-II-sporulation-protein-M	gnl|CDD|376676	pfam01944, SpoIIM, Stage II sporulation protein M. SpoIIM is on e of four stage II sporulation proteins that is necessary for the forespore inside the mother-cell to be properly internalized through the breakdown of peptidoglycans trapped between the membranes of the septum separating the forespore and the mother-cell. The four proteins working in sequence are SpoIIB, pfam05036, SpoIIM, SpoIIP, pfam07454, and finally SpoIID, pfam08486. D, M and P are in a complex with each other and the complex assembles in a hierarchical manner such that M, which serves as a membrane anchor, recruits P to the septum and P, in turn, recruits D to the septum.	4.79452e-35
NZ_CP011130.1|WP_057922949.1|5700980_5702195_-|DUF4350-domain-containing-protein	gnl|CDD|379527	pfam14258, DUF4350, Domain of unknown function (DUF4350). This domain family is found in bacteria, archaea and eukaryotes, and is approximately 70 amino acids in length.	0.000213648
NZ_CP011130.1|WP_082124568.1|5714833_5715457_+|4'-phosphopantetheinyl-transferase-superfamily-protein	gnl|CDD|225002	COG2091, Sfp, Phosphopantetheinyl transferase [Coenzyme metabolism].	2.88652e-24
NZ_CP011130.1|WP_082648760.1|5713214_5714615_-|acyl-CoA-synthetase	gnl|CDD|223442	COG0365, Acs, Acyl-coenzyme A synthetases/AMP-(fatty) acid ligases [Lipid metabolism].	2.05473e-54
NZ_CP011130.1|WP_036107988.1|5711401_5712172_+|exodeoxyribonuclease-III	gnl|CDD|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	6.94129e-139
NZ_CP011130.1|WP_036107957.1|5721379_5721715_+|lipid-A-disaccharide-synthase-N-terminal-domain-containing-protein	gnl|CDD|226461	COG3952, COG3952, Predicted membrane protein [Function unknown].	6.34347e-33
NZ_CP011130.1|WP_057922951.1|5705527_5706040_-|RDD-family-protein	gnl|CDD|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	5.0266e-19
NZ_CP011130.1|WP_036108004.1|5704844_5705528_-|RDD-family-protein	gnl|CDD|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	4.0045e-16
NZ_CP011130.1|WP_057922958.1|5720643_5721369_+|glycosyltransferase-family-2-protein	gnl|CDD|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. DPM1 is the catalytic subunit of eukaryotic dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. In higher eukaryotes,the enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	3.86336e-53
NZ_CP011130.1|WP_036107971.1|5717314_5718232_+|ParB/RepB/Spo0J-family-partition-protein	gnl|CDD|275105	TIGR04285, parB-like_partition_protein, nucleoid occlusion protein. This model describes nucleoid occlusion protein, a close homolog to ParB chromosome partitioning proteins including Spo0J in Bacillus subtilis. Its gene often is located near the gene for the Spo0J ortholog. This protein bind a specific DNA sequence and blocks cytokinesis from happening until chromosome segregation is complete.	3.31066e-71
NZ_CP011130.1|WP_057922952.1|5706936_5708364_+|coniferyl-aldehyde-dehydrogenase	gnl|CDD|143451	cd07133, ALDH_CALDH_CalB, Coniferyl aldehyde dehydrogenase-like. Coniferyl aldehyde dehydrogenase (CALDH, EC=1.2.1.68) of Pseudomonas sp. strain HR199 (CalB) which catalyzes the NAD+-dependent oxidation of coniferyl aldehyde to ferulic acid, and similar sequences, are present in this CD.	0
NZ_CP011130.1|WP_057922955.1|5715644_5716310_+|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG	gnl|CDD|234637	PRK00107, gidB, 16S rRNA (guanine(527)-N(7))-methyltransferase RsmG.	3.41768e-80
NZ_CP011130.1|WP_036108115.1|5706107_5706650_-|gamma-carbonic-anhydrase-family-protein	gnl|CDD|100051	cd04645, LbH_gamma_CA_like, Gamma carbonic anhydrase-like: This family is composed of gamma carbonic anhydrase (CA), Ferripyochelin Binding Protein (FBP), E. coli paaY protein, and similar proteins. CAs are zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide in a two-step mechanism, involving the nucleophilic attack of a zinc-bound hydroxide ion on carbon dioxide, followed by the regeneration of the active site by ionization of the zinc-bound water molecule and removal of a proton from the active site. They are ubiquitous enzymes involved in fundamental processes like photosynthesis, respiration, pH homeostasis and ion transport. There are three evolutionary distinct groups - alpha, beta and gamma carbonic anhydrases - which show no significant sequence identity or structural similarity. Gamma CAs are trimeric enzymes with left-handed parallel beta helix (LbH) structural domain.	5.07384e-73

Protein sequences

>NZ_CP011130.1|WP_036107988.1|5711401_5712172_+|exodeoxyribonuclease-III
MKIVSWNVNSLNVRLPHLEQWLAGFAPDIVALQETKLEDPRFPDTALSAAGYRSVFAGQKTYNGVAIVSRENAQDVQIGIPGFDDEQKRVIAATVGGLRIVNLYVVNGQDVGTDKYAYKLRWLDAVHAWIEQEIRQYPDLIVLGDFNIAPEARDTHDPAVWNEDHILTSTAERDALQRLLSLGLHDAYRLHNQEEGQFSWWDYRQAGFRRNLGLRIDLTLISESLRGRCVAAGIDREPRTWDRPSDHAPAWVELAG
>NZ_CP011130.1|WP_057922954.1|5710125_5711373_+|hypothetical-protein
MNSPAPPAPAPLLKLTGTQIFALCLIVVAIGGWVVLELLADADYPAGQQRFMSVLCIAGSAFAALVTGVLARRVGAALLGWALGLLLGIGGHYLVTQMAAQSARQLQTARHDAIERLLRDAATKREPAALGASMKNLPLSVPGVFCVLADLDSSESAPAYAPAEPVSTDTLMHLGASVAAAGDRAATLAQRQLALRYLLSVLIDRNEPARLPQWLELWRRNQPGGRADAVELVDDVGWDSPENCPNNTGADDLGEVFRAWGIDGLRTWRQAGFRFTDRQQYQLLQYVVDARSLDQLVAAGIDVNASPYPGAGPVPQIALLWHAEQLGQRLAAAEADIAFGMDLDLIAAFVRHGADLRSRDEHGRDACALLNDGLKSAPDRLPVHPRFARARTLLCRAPSGPPAKPSAQPPGAPPP
>NZ_CP011130.1|WP_057922953.1|5708866_5710129_+|hypothetical-protein
MFWYSLAVYPIAAALWLLWITRTYGTAEAGVFDYLDALLTSLAVAAVLPVPVLIWGAYMRKPLQALAGLAFGAIAAVIALPLSMELVGSRRYGQFEHDKAQFAAFEQTVRGGDRARIRAQLRALPGGFSAPRALCGLGGGATYTFERWLWFNDHAYGEPLPSEDLHTAATAVVEGDWPRAEKQAALLTVLRYLLDREETARFPAWARLWRATLEQPDAAAATLTAPAYEGDYGGCDLGDPADPVFRRWHDEGLRMWMQAGFVFADDQHRPALRAVRSKAMLDALFAADPSFAKLLRSEHSLGQEALSAQADDLSARLDRSANPGELADLVEALAKASVDPTLSVSGVSPCRRFDQTEAQRDATKDAPQRRAAAARIRAALCPAGSKPSVAKPRQAEAKAESAATPDDATQPTATQPAPQP
>NZ_CP011130.1|WP_057922952.1|5706936_5708364_+|coniferyl-aldehyde-dehydrogenase
MDILADTPVTDLPATRERLRTAWQARKPDLAQRRADLIRLRDAFRARVPQMDAAIRADFGHRSSHENLLSEAMITLAEIDHAISHLRRWTRPRGASVGWRFWPARAEIRPEPVGVVGILSPWNYPVNLALVPVVSAIAAGNHVFLKPSEHTPRTSQFLRELLADVFPEDRVAVALGGAEVGAAFSALPFDHLLFTGSTAVGRKVMAAAAPHLTPVTLELGGKAPALICADYPIDLAAARIASGKWFNAGQTCIGVDYVLVDAARRDELVAALQKQLRERYGDLHAPQDYTRIINASQYARLSGYLDDARSRGLQVIEPFADPALREQRQAERIFPPALVIDPDPDAQVMQHEIFGPILPVLSYRTLDEAIARINALDRPLALYPFGNDRAQIEKILANTLSGGVTVNDTLLHFGVHDLPFGGIGPSGIGAIHGRNGFDTFSKLLPVFHQRRLVASDLLKPPYKGTIDKMIRWLAK
>NZ_CP011130.1|WP_036108115.1|5706107_5706650_-|gamma-carbonic-anhydrase-family-protein
MSLRPYLDAFPSLGERVYVDPAATVIGAVTLGDDVSIWPGCVVRGDVNSIVIGARTNVQDGTIVHVTHEGPFTRPGGLPTVIANDVTIGHGAIVHACTIDEFALIGMGAKILDGARVSRFGFVGAGAVIAPGKVVGEGELWVGNPARLARTLSEREIEQLQYSAQHYVRLKDRYLGMTPG
>NZ_CP011130.1|WP_057922951.1|5705527_5706040_-|RDD-family-protein
MEDLQNPYAAPTAPPPLPAHAWVDDRTIKADPWIRLVARLIDWGLMMVCFFPLFVAVGLEPDSKDPSPLQLITSCVALLAALGLFIYQLVLLAQSSQTLGKRWMRIKIVRNDGTDASFGRIFGLRMLVIGIIEQVPCIGLMFSLINVVWIFGEESRCLHDLLADTKVVIV
>NZ_CP011130.1|WP_036108004.1|5704844_5705528_-|RDD-family-protein
MLDTYRHVVTPEGVALHLRAAGPLPRALAYVLDLVARIAIYLALYQLLTALFGGAGYAILMLVTFVLSWFYMVLFEVLMQGRTPGKWALGLRVVAADGAPVGWMASFTRNLLRVVDALPVGYAVGLVTSLIDPWGRRLGDMVAGTLVVHAARQQTLYEAQVAPALAPTIVLLQHEQAAVVAFAERAPRLTAARQAELAELVEPLTLSRGQAAVVRLYGIANWLLGRR
>NZ_CP011130.1|WP_036108007.1|5703834_5704848_-|stage-II-sporulation-protein-M
MRQERFVERHQAEWRDFELWLEKRSVSARDARRHRREWTGIADDELPARHRRLCQQLALARRRGYSAVVTDRLQQLMQRGHSVLYQTKPVHWRRAVEFLLAGFPRLVRAEARCMLAAALLFVVPLVTIFVAIQIKPDLAAGLFDAQSLANFEQMYDPAGKGDLGRTNEDDLQMFAHYIGNNVGIGFQTFASGLLAGLGTVFVLIFNGIMIGGVAGHLQAVGHGDPFWRFVAGHSAPELTAIVISGGAGLRLGLSLIAPGQRRRIDSLIHGGRRGAKICIGVFAMLVFAAFVEAFWSSISSVPAPIKYAVGAVLWLLVFAWLLRGGRNAIHRDDEDAA
>NZ_CP011130.1|WP_057922950.1|5702191_5703838_-|DUF4129-domain-containing-protein
MKLEALTVTLRPRTSWEAAELGMALVRRHAGAIWKPWLLVTVPILVLLNAVGWALDLLWLSGLLMWWLKPWFDRIVLFVISRAVFGETPGTRQTVRAQFRWGARWWLPYLTWRRLGPARSLYLPVDLLEGGSGSEARQRRAALGAPVYGMCALLTLVCVHFEILLMIGTLLGAMMFIPFDYLPDTFKALLESFTEQPQWFNAMLNLVAWIAVSVIEPFYVGAGFGLYLNRRTDIEGWDIEIVFRRLRARLAAAAAPSFLALCLTFGWLADAQAQEPAAPAASAMQAPSAQASGDDEEGDEEAYEPTSAPIRGLVDGKKAKRLPSTLNEIYGEQRSDDRAMRDAVAKAMNDPTVAPKRKQMVWKPKHEAKKKKKDEPKPVDPSKFEGLGGGLAAVAKVLMWAVVAVIVGLLLFTLGRWLGWFRGGASEEEQAPPGVRTAVHSEPEPLPDNLPTAIRRLWQAGRHRDALALMYRAAVESMAKRADIVLVPGATEAQCLRASRKLGSAEDRDVFARAVRTWQYAAYAESLPEPQDFDDLVGQLSQRFGWAV
>NZ_CP011130.1|WP_057922949.1|5700980_5702195_-|DUF4350-domain-containing-protein
MNRNLVFTIVGAVVLIAALLLGVSLWRSNYVKVEEEVEEPRSGEAASNPLYILKLALRNDKVKVDARQRLALALHPLQPRDTVLIYRDPRTLSKADADALLGWVERGGHLIVRTPPLRDKLGESPVPVLDTLGLTLLDADDSSPQDQRNDCVGLYERGLEQQSLFCNARRFYYYNSDVEPDYAWGDEDEAYVYARFPRGKGSVDVLADMDFLSNRGNANPLLSAFSFGTDEIAAPANAAFARQLLAPNYRAGTIHLIYAAEVPSLWKTLIFNSWMAWLPLLLWLLGWLWQRTQRFGPLRPAPALERRSLLEHIVASGEHIYRYGYGAILYEAARRAFLLRLRRRDPYAAAQQGQEQVALLVERYKQDPTLGAAAIGDALTQPLTRDHAAFRTRIATLIRMRNRL
>NZ_CP011130.1|WP_036107986.1|5712604_5712880_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MLGIIIWLVVGGVIGWIASMIMRTDGQQGVFLNIIVGIVGAFLGGWLGGVLGIGAGTINSGSFSLGGLVLSLVGAVVLLAIVNLFRRGRVR
>NZ_CP011130.1|WP_082648760.1|5713214_5714615_-|acyl-CoA-synthetase
MSAVFDPSQNALSQDLASPEADVFALVAGASRRALAFGADGIVERARFEREVRALAAALPPAQHAVNLCENRYRFLVALCAVALRGQTNLLPSSRAPAVVEDVLARYPDSYCIGDEALDPAPPRYLQLPSTLAELDGEALRVDARGLLAIGFTSGSTGQPKPNPKTWQAFRTSTAQNLAALGDLLRDDEVTFLVATVPPQHMYGMEMSVLLPLLGPVAVHAQRPFFPGDVARALSDAPTPPLLVTTPVHLRALVESGIELPALAGIVSATAPLPAELAQLAEARYGCEVREVFGSTETCVFARRRTARESAWTPLPGVRVCPQPDGTAIHAPHLPEPVVLADLMEVEADGRFVLRGRSADLLEIAGKRASLGDLTRKLLAIDGVVDGVVFQLDAADAFGVRRIAALVVAPTLSEPQIVHALRQSIDPVFLPRPLRRVNALPRNETGKLPRHALEAMLHADTDSSVE
>NZ_CP011130.1|WP_082124568.1|5714833_5715457_+|4'-phosphopantetheinyl-transferase-superfamily-protein
MSLSGRSPFSADAIHESDDGAVRWTGLTHAHGQPAEPEARRWLAAQLRDPDLSLWRDERQRPHLSPPHQDYDCNWSHSGERLLVALAPRARVGVDLERLQRRPRAIQIAQRYFTAAETAWLAAHPDLDRAFLRLWCAKEAVLKAHGHGLSFGLEKLRFAEHDGALRLIECDPALGEPAQWRLSEIAPEPGYLGALAWRPHENPGASL
>NZ_CP011130.1|WP_057922955.1|5715644_5716310_+|16S-rRNA-(guanine(527)-N(7))-methyltransferase-RsmG
MNTPISLPPALRADLESGLSALALDPVLAAPLLDYLALLARWNRTYNLTAVRDPHEMVGKHLLDSLAMHRYVDGLAQRGGALADLGTGAGLPGIPLAIVKPGLRVTLVESNGKKARFMREALRQLGLKDARVAESRIEAFAEPGAFDAITARALATLPLILELGGHLLKPGGVLLAMKGQRPDEEIAALPDGWEVRAVEALQVPGLVGERHMVTVGRRGEG
>NZ_CP011130.1|WP_057922956.1|5716499_5717318_+|ParA-family-protein
MARIIAVANQKGGVGKTTTAVNLAAALARTPKKVLLVDLDPQGNATMGSGIDKRQLENSVCDVLLGEADAAATIVRTQEDFDLLPGNIDLTAAEISLMNQDEREQRLKRALAPLRGSYDFILIDCPPALSLLTLNALTAADSIIVPMQCEYYALEGLSALVDTIEALKANLNPSLEIEGVLRTMFDVRNNLANAVSADLTTHFGDRVFRTIVPRNVRLAEAPSYGQSIVGYDKASRGGIAYMGLAGEVLRRQRERDQAAKAGARPASAETAA
>NZ_CP011130.1|WP_036107971.1|5717314_5718232_+|ParB/RepB/Spo0J-family-partition-protein
MSNPAKKRGLGRGLEALLGPKAAAEAPALVEAQPGDLLRNLPVDSLSAGKYQPRKHWDEAKLAELAESIKAQGVIQPIVVREIGERGGKTYEIIAGERRWRASRLAGLSTIPVVIREVDDRTVVAMALIENIQREDLNPLEEAQALSRLIDEFDLTHAQAAEAVGRSRAAVSNLLRLLELPAEIRVLVETRALEMGHARALLTLAPQAAIAVARQAAEAGWSVREVEHRVQQLAAGKIPVAGKPKPAKAKPQADIATLERELSESLNTKVNVLHGRAGKGRLVIHYSDLDSLEGVLEKLRGKAVD
>NZ_CP011130.1|WP_036107968.1|5718618_5719050_+|hypothetical-protein
MKWLAAAALMLAPVMASAQTGSCPELKNPELKWSQRQGANYTICYLELPSSLGSGSGFGVYLGNRTFKPNKKARAEKGTVGSQQVQWFKKQTVNNARPYSREALVNLPGDKPKSKVRIYTWIDAATAEQLDEAFGLARQVAVQ
>NZ_CP011130.1|WP_057922957.1|5719352_5720318_+|NAD-dependent-epimerase/dehydratase-family-protein
MTLLVTGAAGFIGANVCRALRAQGRDVVGLDNYNDYYDPQLKRDRVQALCADVDIRALDLGDRDGLAALFDEFAFDRVVHLAAQAGVRYSLSNPHAYVDSNLVGFVNLLELCRHRGVQHLAYASSSSVYGDSAKPPFSEDQRIDQPRSLYAATKAANELMAHTYAHLYGLRSTGLRFFTVYGPWGRPDMAPLLFSRAVLAGRPIDVFNHGKMRRDFTYIDDIVAGVIGALDHPPEQEPPHRVFNLGNHTPVELERFIQVIADAAGRPAEKIYKPMQPGDMIETMADTSRAQAAFGFEPATAIEQGLPRVVAWCRDYFGDDA
>NZ_CP011130.1|WP_057922958.1|5720643_5721369_+|glycosyltransferase-family-2-protein
MTQSPHLSVVVPVFNEQDNVAPLIQEIVTALRGVTDFEIVYVDDHSRDGTLAALEALKAGVPELRVLHHVTQSGQSTAVRNGVKAARGAWIATLDGDGQNDPADIPKLLAKRAESASDVRLFAGWRVNRQDPGSKRWASKWANAIRRRMLRDDTPDTGCGIKLFERAAFLELPYFDHMHRYLPALMQRAGWKTLSVPVNHRQRSTGVSKYNNLNRALVGISDLRGVAWLIRRGKLTQIVER
>NZ_CP011130.1|WP_036107957.1|5721379_5721715_+|lipid-A-disaccharide-synthase-N-terminal-domain-containing-protein
MDFMNSPIEWLTWTGLHMSPWKLIGLVGALMFGGRWLVQFIASKRQGKPVIPRAFWYMSLVGSVMTLSYFVFSQKQDSVGVIQNLFPAFTAAYSLYLDIKHRGWHRDRASH

Crispr_ID: NZ_CP011130_20

• CRISPR_ID: NZ_CP011130_20
• CRISPR_location: 6263232-6263388
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP011130_20

Consensus_repeat	Method
TTGCCTTCGGCGGTCTTGCCCGCGGCCTTGGCGT	CRISPRCasFinder

spacers of NZ_CP011130_20

>20.1|6263266|26|NZ_CP011130|CRISPRCasFinder
CGGCGCCGCACTTGCCCTCGCCGCAC
>20.2|6263326|29|NZ_CP011130|CRISPRCasFinder
TCGCACTCTTGGCCTTGTCGGCACCGCAT

CRISPR arrays and Neighbor proteins around NZ_CP011130_20

CRISPR arrays

The CRISPR arrays of NZ_CP011130_20

>merge|NZ_CP011130|20|6263232-6263388|CRISPRCasFinder
TTGCCTTCGGCGGTCTTGCCCGCGGCCTTGGCGTCGGCGCCGCACTTGCCCTCGCCGCACTTGCCTTCGGCGGTCTTGCCGGCGGCCTTGGCGTTCGCACTCTTGGCCTTGTCGGCACCGCATTTGCCTTCGCCGCACTTGCCTTCGCCTGCGGCGT

>NZ_CP011130|20|19|6263232-6263388|CRISPRCasFinder
TTGCCTTCGGCGGTCTTGCCCGCGGCCTTGGCGT	CGGCGCCGCACTTGCCCTCGCCGCAC
TTGCCTTCGGCGGTCTTGCCGGCGGCCTTGGCGT	TCGCACTCTTGGCCTTGTCGGCACCGCAT
TTGCCTTCGCCGCACTTGCCTTCGCCTGCGGCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_057923291.1|6265075_6267442_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP011130.1|WP_057923284.1|6255090_6256011_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176114
NZ_CP011130.1|WP_057923290.1|6264530_6264782_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923286.1|6257831_6259208_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP011130.1|WP_057923283.1|6254291_6254990_-|pirin-family-protein	unknown	unknown	gnl|CDD|380375
NZ_CP011130.1|WP_057923293.1|6272559_6273579_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349893
NZ_CP011130.1|WP_057923287.1|6260648_6261320_-|hypothetical-protein	unknown	unknown	gnl|CDD|225338
NZ_CP011130.1|WP_036113074.1|6271800_6272406_-|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl|CDD|212030
NZ_CP011130.1|WP_057923282.1|6253400_6254231_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP011130.1|WP_036113290.1|6273607_6274573_-|membrane-protein	unknown	unknown	gnl|CDD|223701
NZ_CP011130.1|WP_057923289.1|6263625_6264300_-|DoxX-family-protein	unknown	unknown	gnl|CDD|225168
NZ_CP011130.1|WP_057923292.1|6270777_6271671_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176150
NZ_CP011130.1|WP_036113065.1|6268468_6269776_+|hypothetical-protein	unknown	unknown	gnl|CDD|238287
NZ_CP011130.1|WP_036113068.1|6269914_6270691_-|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl|CDD|225158
NZ_CP011130.1|WP_057923757.1|6261309_6262077_-|putative-DNA-binding-domain-containing-protein	unknown	unknown	gnl|CDD|225760
NZ_CP011130.1|WP_057923288.1|6262069_6262921_-|DUF692-domain-containing-protein	unknown	unknown	gnl|CDD|235447
NZ_CP011130.1|WP_036113045.1|6259204_6259945_-|response-regulator	unknown	unknown	gnl|CDD|181883
NZ_CP011130.1|WP_082648825.1|6260073_6260652_-|thioredoxin-family-protein	unknown	unknown	gnl|CDD|239310
NZ_CP011130.1|WP_057923285.1|6256027_6257665_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP011130.1|WP_148650665.1|6267866_6268469_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057923291.1|6265075_6267442_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	3.84896e-45
NZ_CP011130.1|WP_057923284.1|6255090_6256011_+|LysR-family-transcriptional-regulator	gnl|CDD|176114	cd08422, PBP2_CrgA_like, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA and its related homologs, contains the type 2 periplasmic binding domain. This CD includes the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA and its related homologs. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.76554e-82
NZ_CP011130.1|WP_057923286.1|6257831_6259208_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	5.7258e-41
NZ_CP011130.1|WP_057923283.1|6254291_6254990_-|pirin-family-protein	gnl|CDD|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	3.30589e-70
NZ_CP011130.1|WP_057923293.1|6272559_6273579_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349893	cd05640, M28_like, M28 Zn-peptidase; uncharacterized subfamily. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions.	4.42073e-73
NZ_CP011130.1|WP_057923287.1|6260648_6261320_-|hypothetical-protein	gnl|CDD|225338	COG2717, COG2717, Predicted membrane protein [Function unknown].	0.000123953
NZ_CP011130.1|WP_036113074.1|6271800_6272406_-|LysM-peptidoglycan-binding-domain-containing-protein	gnl|CDD|212030	cd00118, LysM, Lysin Motif is a small domain involved in binding peptidoglycan. LysM, a small globular domain with approximately 40 amino acids, is a widespread protein module involved in binding peptidoglycan in bacteria and chitin in eukaryotes. The domain was originally identified in enzymes that degrade bacterial cell walls, but proteins involved in many other biological functions also contain this domain. It has been reported that the LysM domain functions as a signal for specific plant-bacteria recognition in bacterial pathogenesis. Many of these enzymes are modular and are composed of catalytic units linked to one or several repeats of LysM domains. LysM domains are found in bacteria and eukaryotes.	3.02513e-07
NZ_CP011130.1|WP_057923282.1|6253400_6254231_-|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	8.10038e-45
NZ_CP011130.1|WP_036113290.1|6273607_6274573_-|membrane-protein	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	1.73137e-09
NZ_CP011130.1|WP_057923289.1|6263625_6264300_-|DoxX-family-protein	gnl|CDD|225168	COG2259, COG2259, Predicted membrane protein [Function unknown].	9.04989e-16
NZ_CP011130.1|WP_057923292.1|6270777_6271671_+|LysR-family-transcriptional-regulator	gnl|CDD|176150	cd08461, PBP2_DntR_like_3, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator similar to DntR, which is involved in the catabolism of dinitrotoluene; contains the type 2 periplasmic binding fold. This CD includes an uncharacterized LysR-type transcriptional regulator similar to DntR, NahR, and LinR, which are involved in the degradation of aromatic compounds. The transcription of the genes encoding enzymes involved in such degradation is regulated and expression of these enzymes is enhanced by inducers, which are either an intermediate in the metabolic pathway or compounds to be degraded. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.28901e-92
NZ_CP011130.1|WP_036113065.1|6268468_6269776_+|hypothetical-protein	gnl|CDD|238287	cd00519, Lipase_3, Lipase (class 3). Lipases are esterases that can hydrolyze long-chain acyl-triglycerides into di- and monoglycerides, glycerol, and free fatty acids at a water/lipid interface. A typical feature of lipases is "interfacial activation," the process of becoming active at the lipid/water interface, although several examples of lipases have been identified that do not undergo interfacial activation . The active site of a lipase contains a catalytic triad consisting of Ser - His - Asp/Glu, but unlike most serine proteases, the active site is buried inside the structure. A "lid" or "flap" covers the active site, making it inaccessible to solvent and substrates. The lid opens during the process of interfacial activation, allowing the lipid substrate access to the active site. .	0.0002432
NZ_CP011130.1|WP_036113068.1|6269914_6270691_-|NAD(P)H-dependent-oxidoreductase	gnl|CDD|225158	COG2249, MdaB, Putative NADPH-quinone reductase (modulator of drug activity B) [General function prediction only].	4.68265e-63
NZ_CP011130.1|WP_057923757.1|6261309_6262077_-|putative-DNA-binding-domain-containing-protein	gnl|CDD|225760	COG3219, COG3219, Uncharacterized protein conserved in bacteria [Function unknown].	3.85419e-60
NZ_CP011130.1|WP_057923288.1|6262069_6262921_-|DUF692-domain-containing-protein	gnl|CDD|235447	PRK05409, PRK05409, hypothetical protein; Provisional.	8.67819e-147
NZ_CP011130.1|WP_036113045.1|6259204_6259945_-|response-regulator	gnl|CDD|181883	PRK09468, ompR, osmolarity response regulator; Provisional.	1.08244e-77
NZ_CP011130.1|WP_082648825.1|6260073_6260652_-|thioredoxin-family-protein	gnl|CDD|239310	cd03012, TlpA_like_DipZ_like, TlpA-like family, DipZ-like subfamily; composed uncharacterized proteins containing a TlpA-like TRX domain. Some members show domain architectures similar to that of E. coli DipZ protein (also known as DsbD). The only eukaryotic members of the TlpA family belong to this subfamily. TlpA is a disulfide reductase known to have a crucial role in the biogenesis of cytochrome aa3.	1.43415e-73
NZ_CP011130.1|WP_057923285.1|6256027_6257665_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl|CDD|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	1.80845e-112

Protein sequences

>NZ_CP011130.1|WP_057923288.1|6262069_6262921_-|DUF692-domain-containing-protein
MRTLPSLSAGLGLRRGLLPSLLAMDDDAVDFLEVAPDNWIGVGGQFGEALSELSARFPLSCHGLSLSLGGSAPLDMDLLRAMRQFNDRHGIGLYSEHLSYCADDGHLYDLMPIPFTDEAIGHVAARIRQVQDVLGRRIAVENVSYYAAPYQALAEIDFIRAVLDEADCDLLLDVNNLYVNAINHGYDAQAFLARLPGERIASYHIAGHFDEAADLKVDTHGAPVKADVWSLLDSAYRRFGVRPTLLERDFNFPPLPELLAETDRIRAMQTSHADVAQPEPAHA
>NZ_CP011130.1|WP_057923757.1|6261309_6262077_-|putative-DNA-binding-domain-containing-protein
MHETLREQQSVLARHLRDPARHPSPPGLEARRMRVYRELFLGSIESLLAGGFPVIRQTLGAADWSALVQAFYARHRSRTPLFTRIAGEFVEFIETQADDPALPPWLPELAHYEWVEQALLISDAQAPAHDPDGDLLDGRPLLSSLAMPLAYRWPVLEIGPSHIPQAPPPQATTLLVHRDRDHQVRFARIAPLAYQLLTSLQVNAYRGREHLAALAAQTGGDAEQLHIHGLGLLRQLREQGVVLGTHLATEPCDER
>NZ_CP011130.1|WP_057923287.1|6260648_6261320_-|hypothetical-protein
MNANYRFPRGWSLFWLIGALILTMSALILALNPDTTEAVRSVIRATARSSFALFLLAFVASSLATLVPNEFTRGLMRERRYIGLSFAFSHFVHLLAIIAYGVLNPQFWPGRSALTNAPGTLGYVFIALLALTSFRFASRHMTAAAWKRLHTAGIWVIAAIFGYSFFKRIPSMSVLYAIPFSILCAAVAVRLVGKWAQANKRRQARTRSLDRTSSFPNAVEPSP
>NZ_CP011130.1|WP_082648825.1|6260073_6260652_-|thioredoxin-family-protein
MTLPQNAAVAGAANSNRCAIWRSAIAGLALCLSAAACTPAAHADAARAVAAPEFAGTARWFNTPALSMAGLRGKVVLVEFWTYSCINCLRVAPHVKQWHERYRDQGLVVIGVHTPEYDEEHSAGNLQAAIKRLGIDYPVAQDNDYATWNAYGNRFWPALYLIDRDGRIVYRHYGEGEYDVTDARIRALLARR
>NZ_CP011130.1|WP_036113045.1|6259204_6259945_-|response-regulator
MDHVDHILVVDDDREIRQMVADYLHKNGLRATVAADGREMRALLDTHAVDLIVLDLMMPGEDGLTLCRNLRAGKHRAIPVVMLTARDDQTDRIIGLEMGADDYVTKPFAARELLARIKAVIRRTRMLPPNLQVTQASRTIAFGRWRLDTTARHLLDPDDTVVALSGAEFRLLHVFLDHANRVLTRDQLLNLTQGRDAEHFERSIDLLVSRLRQRLQDDAREQSYIKTVRSEGYVFSMPVSLLGDGE
>NZ_CP011130.1|WP_057923286.1|6257831_6259208_-|HAMP-domain-containing-histidine-kinase
MNANTNAAPTPAARRGSRWLPRTLASRLSLILLSGLLIAHALSFGLLFYERYTAATSMLMSNLEQDVVVAVNLLDRLPPQERERWLPLLRRRTFHYMLDDGAADAAARNEPPVGGTSRDMAEMIASALGPRYPTRANAVPGDGEHFQVHLKLSDGAAMVIDVRPSVMPLAKWLPYVLAIQLALLLLCTWAAVRLTTRPLGRLAKAAETLHPAGEGERLPVGGPTEVAQAITAFNAMQDRIAHYMRERLQILAAISHDLQTPITRMQLRAEAMDESSERDKMFDDLGQMQHLVREGIAYARSAHGASEPAVRIDLNAFLDSLVCDYLDTDRPVTFAGRVDGPVTTRPHALRRIVGNLIDNAIHYAGAAELELDHDPAGGVRIQVRDRGPGIPQDELGKVMQPFYRLEASRNRSTGGTGLGLAIAQQLAESIGATLLLRNRDGGGLEAILRIAGPIVAAR
>NZ_CP011130.1|WP_057923285.1|6256027_6257665_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MTDVSFRGLCLRATNLGFSWPDGTPVFDGLSCSFGPQRSGLVGPNGSGKSTLMRLLAGQLKPTAGQVETHGVVAYLPQHLPLSGEASVAQVLGVHAKLDALRAIAEGAADPSLLDIVGEDWDLEERTRADLARLGLSDIALQRRLDSFSGGEIVSLGIAAQLLRRPDLLLLDEPSNNLDRASRQHLYRLVETWRGGLIVVSHDRELLERMDQIAEIGPSALRVYGGCFGFYQAAVDGQTQAAQQDVRNLRQQVKREQREQQQARERAERRSGNAGRSLASAGLPRIVAGNRKRGAQVAAGKSADVHSARLEEARQRLGEARRGLRESSELDLSLPATRVPTERLLFDGRQLQLRRGGRALFAGGGVDIAIRGPERIAILGANGAGKSSLLRMIAGELAPDAGDVRRGAGRIASLSQRLDALDPDASVAANFAARTAHLSPLERANLLARWLFRGDRGQLPVGALSGGERLRICLACVLHAQPAPQLLLLDEPTNNLDLSTIEDLERALRAYEGALLVVSHDERFIEAIGITRRLLLAQGRLQEPR
>NZ_CP011130.1|WP_057923284.1|6255090_6256011_+|LysR-family-transcriptional-regulator
MNKLPDLEAWAIFAKVAETGSFARTAAEFGLAQATVSKAVTRLETRLKTVLFHRTSRRMSLTESGRGALERATRILAEGEAVEAEITAQAKSPSGQVRIAVPMSFGIAHLSPLLPEFMKRYPDIALEIVFDDGVTDLVGGGYDLALRISSLADSSLLARRLCGVRIVLVGSPAYFETYGRPSHPRELSEHRALLYTYSRFGNAWRFSHRRHGDFSISLPTPLRVNNAEALNPALLAGLGLALQPEFLVWRELRNGKLEIAMPEWSPPPIALHIVTPPGRMRPQRVQALIDYLARKFEKAPWADPDG
>NZ_CP011130.1|WP_057923283.1|6254291_6254990_-|pirin-family-protein
MIELRPYDSLGGANHGWLDAKHHFAFAGYHDPARMGWGALRVWNDDTIQANTGFPPHSHADMEIITYVRDGAISHQDNLGNRGRTEAGDVQVMSAGSGIQHAEYNLEAQTTRIFQIWIIPDQRGGAPTWGAKPFPKGDRAGRFVVLASGKGDEDTLPIRADARVLGLTLAAGESAEYVFGDNRYGYLVPAKGVVEIDGLRVQARDGAAIRDQASIRVTALEDAELVLVDTAP
>NZ_CP011130.1|WP_057923282.1|6253400_6254231_-|alpha/beta-hydrolase
MGTFTTKDGVQIYYKDWGPSDGEPVVFSHGWPLSADSWESQMLFLASNGYRTIAHDRRGHGRSSQPWDGNDMDHYADDLGQLLEHLDLRGATLFGFSTGGGEVARYIGRHGTTRVKKAGLISSVPPLMLKTDANPGGLPLEVFDGLREASIADRSQLYQDLASGPFFGFNRDGAKKSQGMIDSFWAQGMQGGHKNTYDSIAAFSATDFTEDLKKFDVPTLIVHGDDDQVVPIDAAGRASAKLVPNNKLIVYPGAPHGLTDTHKDKLNQDLLAFLKS
>NZ_CP011130.1|WP_057923289.1|6263625_6264300_-|DoxX-family-protein
MSVDSTPAAPLMSRVDGVAPWLAPLGLRVLLAWEFFEAGREKLQGDNWFADLGDKFPLPFSLLGADLNWTLATWTELAGAAALLIGLGTRYVAAALWVLTVVAIYAVHWPSDWSSLAELWQGYAISNQGHGNYKLPLIYLAMLLPLMLGGGGRLSIDRLLASRRAPVAAASADAPAWGVVLLGIGATVSLLLPWVGATLAFAGIALTIKPRGRHAAKRLSSTAA
>NZ_CP011130.1|WP_057923290.1|6264530_6264782_+|hypothetical-protein
MIRTSGIALAALYLIGCAGDAPPTSGECRALLQSRTATRTEMVAFIVRAKRDLDAAPRNRIDSHTEGLGLCTGALMRKAQSIK
>NZ_CP011130.1|WP_057923291.1|6265075_6267442_-|TonB-dependent-receptor
MSLYPEARLPLRGGAAVSRRPLAMTALARACSALLLVCAATAASAQDAPQAAAPATAQSATSLDAVTVTAERREQNLQDVPVSVGVMQGDAMRALTAGGDDTLLALSGRVPSLYAETTTGRIFPRFYIRGLGNIDFYLGASQPVSIIQDDVVLEHVVLKSNPVFDTDQVEVLRGPQGSLFGRNTTAGIIKFDSIKPSQDFSGRVQASVGSYNTVSIDGGIGGPINDVLSFRVSTLYQHRDDWVDNTFAGASADGTVTPKKDAMGGFDDRNLRVQLLLAPSENFSILVSAHARDYSGTSTLFLRNAIVKGSNEVDVPRDKVAFDEAGNNPQAYKTYGGSIKASYNFGETSLTSISAYETTSGYSRGDTDGGAAANYPVRGVPNGFGQSMGQIRDLDQFTQEFRLASETDDALQWQVGAFYFDGRDVTDFYQRAWFLKGPARNPNNWVRLRNSNTSWAAFGQLSYKVSDALTLTAGLRQTRDTKETRLLKTADTAAGVSTYTGRRDVRLSDTQPSWDLSAMYEINPNLSVYAKVARGFRGPTIQGRSAVFNADFTTADSETILSWEAGIKSSLFDNRLRLNATAFTYTVDDIQLNGNDSNGNGVLFNADKARACGVEADLDWRPIPNLSLTAGVSLLHSEIQDKRVYAQVCALNGAVVCTVEDPTIKVGANTFAQIDGNPLPNAPKYSVNLGARYDIPLSDSGALFVATDWNKQGYTSFVLYDSKEFNASGNFEGGLKVGYTGGYGAYEVALFARNITNEKNLKGVIENYMAAVYNEPRIVGVSVNVNWH
>NZ_CP011130.1|WP_148650665.1|6267866_6268469_+|hypothetical-protein
MSMHSAARANPPQAPSLFTAPAPVAAPVVKLNPHARDGHVLSFHFDDLPQALTQVTATADFQVANVECVPVDYGKAIGGVRLAPRHSLPLSLNRGDDGRYVAIVHVDALLDEDYYGLGVCRWELTTATVHFHSPSTHFVGGLKAERLIAGGETVQYYLTRDLAQKPRSMDYVYGETAADFYQPSAGPQFTLVLNAHKEVP
>NZ_CP011130.1|WP_036113065.1|6268468_6269776_+|hypothetical-protein
MPSSQDYAALSQDAYNDRRADPTVSVPINGVDYRVLATANNRENGYQGTIYQRVDSGEIIVAHRGTEPTNGVGEFIRDVIRTDGGMVVNGVNNQAPDAIALTQRAIDIAREQGERTGRPQPPVAVTGHSLGGTLAQISAHRFQAEGVHGETFNAYGAAGLNMGIPAGDNNRMINHVRASDTVSSASPQYGQTRVYATQEDVDALRDAGYANNRRQSFWPDFIGGDLRNPVGVVASRGLAAHDIAPFAGGPGTPPLMTRANEDRAQQFDPMIDKFRGDIGAARAGITGASQNVQDGIRRVREGWNDLFSHNGHVQGAPLVSDSPLLGQTYAAIDRGGPALAGLDHRAVASLTATAGAQGLHEIHHVARGNNGTLFAVQGQSPNDPAALRASVDLETQRQPLAVSSQQSVQQAEQAQRNNGAQQEAVEQTRRNPSMV
>NZ_CP011130.1|WP_036113068.1|6269914_6270691_-|NAD(P)H-dependent-oxidoreductase
MNVLLIYAHPEPRSLNGSLRDFTIQRLRQAGHSVQVSDLYAMRWKAAIDADDSTDQDPDARFDPARDSKRAFDSGTQREDIAREQDKLRWADTVILQFPLWWFSMPAILKGWVDRVYAYGFAYGVGEHSDRHWGDRYGEGSLAGKRAMLVVTAGGWESHYGPRGINGPIDDVLFPIQHGVLYYPGFSVLPPFVVYRSSRTDEARFADLCDALGQRLDALETTAPIAYRRQNAGDYEIPALTLREHIAPERVGFAAHIE
>NZ_CP011130.1|WP_057923292.1|6270777_6271671_+|LysR-family-transcriptional-regulator
MTNLRRLDLNLLVTLDALLSEHSVTRAAQRLNFSQPSISVHLAKLRDVFADPLLLPGPRGMRPTARADELREPLRQALAALERAVSPAAAFDPAQADRTWRVAASDYSESTVLLPALIGLRAAAPGTRLAVVEASPARIARQAEQGDIDLAFHTSHDAPSGLRRRTLFAERYVLVGRAGHPRLKRRPTLAQFCKLDHVIVSPDGGGFHGVTDDALAPLGLRRRVVLSVPHFLFVRSVLATTDLVAMLPARLVRDMPALRVVEPPVEVPGYEMAMLWHERVHRDPAHQWLREHIAGSV
>NZ_CP011130.1|WP_036113074.1|6271800_6272406_-|LysM-peptidoglycan-binding-domain-containing-protein
MTALNGPSYAGPQLGALVNTKSEVETAQVVTPSGMKPIVVQPGDNLSQIAADNKIPLAELLAANPQFSLDPASNPNTRSADLIYPGEVVFAPTAEAKATDAAGAKYDTAIQASEQLSTNRGEWEDKSKDVTTTKNDFKQAVQAEIDAGMSYSGNSREDYGNEAVALGEQIAQRYEAQGKPELAAAAREAAQERSTAINNEV
>NZ_CP011130.1|WP_057923293.1|6272559_6273579_-|M20/M25/M40-family-metallo-hydrolase
MLKFLRRIAYLIAIVAAIAGLIVFAVVQPWVRPIASTPPAADPQRLRFDVKHLSVDLYPRSYDQTETLDQAARYIHEQLRLAGAQVSYQDVPVEGMVYRNVIGRFGPATGPLRVIGAHYDSFADVGIENDDPRGYSPKTHTPGADDNASGVAGLLELARMLGRSEQTRPIELVAYTLEEPPHFRSEHMGSAHHARSLRAAGREVEYMLSLEMIGRFSDRPGSQRYPLRGMHRLYPDRGDFAVLVGRMGDFGQTRALKATMAGATDLPVHSISAPPLLVQGVDFSDHLSYWAQGYPAWMVSDTAFLRSDTYHQASDTYDRLDYPRMAKVVQAVYAMSQRP
>NZ_CP011130.1|WP_036113290.1|6273607_6274573_-|membrane-protein
MALTGMYLVLRLGLVGALLSGLLVFQLIHVLAPLVERKVRGDRARIIAVAVLASVIIGLLILAVLGLVTFFRVDTGGEQALLARVMEIIDASRGQIPPWAQPYLPDDMSDLKRAVSAWLEAHRGELSLAGAEAAQVAVRLIIGMVLGAMIALYDEQPIGRLGPLATELLGRASRFADAFRRVVFAQIKISLLNTTFTAIFLLIVLPLFGIRLPLAKTLVAITFVAGLLPVIGNLISNTLITVAALSISLYVAIAALAYLVVIHKLEYFLNARIVGGEIQARAWELLLAMLVMEAAFSMPGLIVGPIYYAYIKRELVDQRWI

Crispr_ID: NZ_CP011130_21

• CRISPR_ID: NZ_CP011130_21
• CRISPR_location: 6298762-6298879
• CRISPR_type: Orphan
• Repeat_type: I-E
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_21

Consensus_repeat	Method
CGCCGAAGTAAGGCAGAGCCCGCTTTCGCGGGAATGACG	CRISPRCasFinder

spacers of NZ_CP011130_21

>21.1|6298801|40|NZ_CP011130|CRISPRCasFinder
TTCTGGTGAGATGGCGCTGAAGGCTCTGGATATTCGGCTA

CRISPR arrays and Neighbor proteins around NZ_CP011130_21

CRISPR arrays

The CRISPR arrays of NZ_CP011130_21

>merge|NZ_CP011130|21|6298762-6298879|CRISPRCasFinder
CGCCGAAGTAAGGCAGAGCCCGCTTTCGCGGGAATGACGTTCTGGTGAGATGGCGCTGAAGGCTCTGGATATTCGGCTACGCCGAAGTAAGGCAGAGCCCGCCTTCGCGGGAATGACG

>NZ_CP011130|21|20|6298762-6298879|CRISPRCasFinder
CGCCGAAGTAAGGCAGAGCCCGCTTTCGCGGGAATGACG	TTCTGGTGAGATGGCGCTGAAGGCTCTGGATATTCGGCTA
CGCCGAAGTAAGGCAGAGCCCGCCTTCGCGGGAATGACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_148650671.1|6286345_6288493_-|aminodeoxychorismate-synthase-component-I	unknown	unknown	gnl|CDD|223225
NZ_CP011130.1|WP_057923307.1|6292193_6293837_-|M4-family-metallopeptidase	unknown	unknown	gnl|CDD|341060
NZ_CP011130.1|WP_057923309.1|6300641_6301157_+|cytochrome-c5-family-protein	unknown	unknown	gnl|CDD|225784
NZ_CP011130.1|WP_148650673.1|6308039_6308408_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923310.1|6301863_6303660_+|ExeM/NucH-family-extracellular-endonuclease	unknown	unknown	gnl|CDD|225249
NZ_CP011130.1|WP_036113138.1|6307321_6307717_+|HU-family-DNA-binding-protein	unknown	unknown	gnl|CDD|259856
NZ_CP011130.1|WP_057923312.1|6304649_6305729_+|DUF1311-domain-containing-protein	unknown	unknown	gnl|CDD|226868
NZ_CP011130.1|WP_036113111.1|6296145_6296553_-|DUF350-domain-containing-protein	unknown	unknown	gnl|CDD|226289
NZ_CP011130.1|WP_057923314.1|6308555_6309362_+|hypothetical-protein	unknown	unknown	gnl|CDD|226100
NZ_CP011130.1|WP_036113107.1|6295516_6296137_-|DUF1190-domain-containing-protein	unknown	unknown	gnl|CDD|377691
NZ_CP011130.1|WP_057923308.1|6294234_6295428_-|glutathionylspermidine-synthase-family-protein	unknown	unknown	gnl|CDD|367631
NZ_CP011130.1|WP_036113114.1|6296617_6297289_-|DUF2491-family-protein	unknown	unknown	gnl|CDD|371191
NZ_CP011130.1|WP_057923304.1|6288577_6289291_-|4'-phosphopantetheinyl-transferase-superfamily-protein	unknown	unknown	gnl|CDD|225524
NZ_CP011130.1|WP_148650672.1|6291556_6292066_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923305.1|6289564_6291223_-|M4-family-metallopeptidase	unknown	unknown	gnl|CDD|341060
NZ_CP011130.1|WP_057923311.1|6303898_6304597_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|225496
NZ_CP011130.1|WP_036113117.1|6297410_6298466_-|two-pore-domain-potassium-channel-family-protein	unknown	unknown	gnl|CDD|369572
NZ_CP011130.1|WP_036113304.1|6305764_6306847_+|cell-division-protein-ZapE	unknown	unknown	gnl|CDD|224402
NZ_CP011130.1|WP_036113120.1|6299014_6299779_-|PspA/IM30-family-protein	unknown	unknown	gnl|CDD|281941
NZ_CP011130.1|WP_036113123.1|6299775_6300192_-|DUF2170-family-protein	unknown	unknown	gnl|CDD|378318

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_148650671.1|6286345_6288493_-|aminodeoxychorismate-synthase-component-I	gnl|CDD|223225	COG0147, TrpE, Anthranilate/para-aminobenzoate synthases component I [Amino acid transport and metabolism / Coenzyme metabolism].	2.98081e-143
NZ_CP011130.1|WP_057923307.1|6292193_6293837_-|M4-family-metallopeptidase	gnl|CDD|341060	cd09597, M4_TLP, Peptidase M4 family including thermolysin, protealysin, aureolysin, and neutral protease. This peptidase M4 family includes several endopeptidases such as thermolysin (EC 3.4.24.27), aureolysin (the extracellular metalloproteinase from Staphylococcus aureus), neutral protease from Bacillus cereus, protealysin, and bacillolysin (EC 3.4.24.28). Typically, the M4 peptidases consist of a presequence (signal sequence), a propeptide sequence, and a peptidase unit. The presequence is cleaved off during export while the propeptide has inhibitory and chaperone functions and facilitates folding. The propeptide remains attached until the peptidase is secreted and can be safely activated. All peptidases in this family bind a single catalytic zinc ion which is tetrahedrally co-ordinated by three amino acid ligands and a water molecule that forms the nucleophile on activation during catalysis. The active site is found between two sub-domains; the N-terminal domain contains the HEXXH zinc-binding motif while the helical C-terminal domain, which is unique for the family, carries the third zinc ligand. These peptidases are secreted eubacterial endopeptidases from Gram-positive or Gram-negative sources that degrade extracellular proteins and peptides for bacterial nutrition. They are selectively inhibited by Steptomyces metalloproteinase inhibitor (SMPI) as well as by phosphoramidon from Streptomyces tanashiensis. A large number of these enzymes are implicated as key factors in the pathogenesis of various diseases, including gastritis, peptic ulcer, gastric carcinoma, cholera and several types of bacterial infections, and are therefore important drug targets. Some enzymes of the family can function at extremes of temperatures, while some function in organic solvents, thus rendering them novel targets for biotechnological applications. Thermolysin is widely used as a nonspecific protease to obtain fragments for peptide sequencing. It has also been used in production of the artificial sweetener aspartame.	6.20924e-89
NZ_CP011130.1|WP_057923309.1|6300641_6301157_+|cytochrome-c5-family-protein	gnl|CDD|225784	COG3245, CycB, Cytochrome c5 [Energy production and conversion].	4.80024e-17
NZ_CP011130.1|WP_057923310.1|6301863_6303660_+|ExeM/NucH-family-extracellular-endonuclease	gnl|CDD|225249	COG2374, COG2374, Predicted extracellular nuclease [General function prediction only].	4.14861e-94
NZ_CP011130.1|WP_036113138.1|6307321_6307717_+|HU-family-DNA-binding-protein	gnl|CDD|259856	cd13834, HU_like, DNA-binding proteins similar to HU domains. This subfamily consists of DNA-binding proteins similar to HU domains. HU is a conserved nucleoid-associated protein (NAP) which binds non-specifically to duplex DNA with a particular preference for targeting nicked and bent DNA. It is highly basic and contributes to chromosomal compaction and maintenance of negative supercoiling, thus often referred to as histone-like protein. HU can induce DNA bends, condense DNA in a fiber and also interact with single stranded DNA. It contains two homologous subunits, alpha and beta, typically forming homodimers (alpha-alpha and beta-beta), except in E. coli and other enterobacteria, which form heterodimers (alpha-beta).	1.24462e-29
NZ_CP011130.1|WP_057923312.1|6304649_6305729_+|DUF1311-domain-containing-protein	gnl|CDD|226868	COG4461, LprI, Uncharacterized protein conserved in bacteria, putative lipoprotein [Function unknown].	2.60281e-14
NZ_CP011130.1|WP_036113111.1|6296145_6296553_-|DUF350-domain-containing-protein	gnl|CDD|226289	COG3766, COG3766, Predicted membrane protein [Function unknown].	9.06233e-29
NZ_CP011130.1|WP_057923314.1|6308555_6309362_+|hypothetical-protein	gnl|CDD|226100	COG3570, StrB, Streptomycin 6-kinase [Defense mechanisms].	3.91906e-96
NZ_CP011130.1|WP_036113107.1|6295516_6296137_-|DUF1190-domain-containing-protein	gnl|CDD|377691	pfam06693, DUF1190, Protein of unknown function (DUF1190). This family consists of several hypothetical Enterobacterial proteins of around 212 residues in length and is known as YjfM in Escherichia coli. The function of this family is unknown.	2.02103e-24
NZ_CP011130.1|WP_057923308.1|6294234_6295428_-|glutathionylspermidine-synthase-family-protein	gnl|CDD|367631	pfam03738, GSP_synth, Glutathionylspermidine synthase preATP-grasp. This region contains the Glutathionylspermidine synthase enzymatic activity EC:6.3.1.8. This is the C-terminal region in bi-enzymes. Glutathionylspermidine (GSP) synthetases of Trypanosomatidae and Escherichia coli couple hydrolysis of ATP (to ADP and Pi) with formation of an amide bond between spermidine and the glycine carboxylate of glutathione (gamma-Glu-Cys-Gly). In the pathogenic trypanosomatids, this reaction is the penultimate step in the biosynthesis of the antioxidant metabolite, trypanothione (N1,N8-bis-(glutathionyl)spermidine), and is a target for drug design. This region, the pre-ATP grasp region, probably carries the substrate-binding site.	0
NZ_CP011130.1|WP_036113114.1|6296617_6297289_-|DUF2491-family-protein	gnl|CDD|371191	pfam10679, DUF2491, Protein of unknown function (DUF2491). This is a bacterial family of uncharacterized proteins.	8.4997e-52
NZ_CP011130.1|WP_057923304.1|6288577_6289291_-|4'-phosphopantetheinyl-transferase-superfamily-protein	gnl|CDD|225524	COG2977, EntD, Phosphopantetheinyl transferase component of siderophore synthetase [Secondary metabolites biosynthesis, transport, and catabolism].	5.1632e-45
NZ_CP011130.1|WP_057923305.1|6289564_6291223_-|M4-family-metallopeptidase	gnl|CDD|341060	cd09597, M4_TLP, Peptidase M4 family including thermolysin, protealysin, aureolysin, and neutral protease. This peptidase M4 family includes several endopeptidases such as thermolysin (EC 3.4.24.27), aureolysin (the extracellular metalloproteinase from Staphylococcus aureus), neutral protease from Bacillus cereus, protealysin, and bacillolysin (EC 3.4.24.28). Typically, the M4 peptidases consist of a presequence (signal sequence), a propeptide sequence, and a peptidase unit. The presequence is cleaved off during export while the propeptide has inhibitory and chaperone functions and facilitates folding. The propeptide remains attached until the peptidase is secreted and can be safely activated. All peptidases in this family bind a single catalytic zinc ion which is tetrahedrally co-ordinated by three amino acid ligands and a water molecule that forms the nucleophile on activation during catalysis. The active site is found between two sub-domains; the N-terminal domain contains the HEXXH zinc-binding motif while the helical C-terminal domain, which is unique for the family, carries the third zinc ligand. These peptidases are secreted eubacterial endopeptidases from Gram-positive or Gram-negative sources that degrade extracellular proteins and peptides for bacterial nutrition. They are selectively inhibited by Steptomyces metalloproteinase inhibitor (SMPI) as well as by phosphoramidon from Streptomyces tanashiensis. A large number of these enzymes are implicated as key factors in the pathogenesis of various diseases, including gastritis, peptic ulcer, gastric carcinoma, cholera and several types of bacterial infections, and are therefore important drug targets. Some enzymes of the family can function at extremes of temperatures, while some function in organic solvents, thus rendering them novel targets for biotechnological applications. Thermolysin is widely used as a nonspecific protease to obtain fragments for peptide sequencing. It has also been used in production of the artificial sweetener aspartame.	1.44668e-81
NZ_CP011130.1|WP_057923311.1|6303898_6304597_+|alpha/beta-fold-hydrolase	gnl|CDD|225496	COG2945, COG2945, Predicted hydrolase of the alpha/beta superfamily [General function prediction only].	8.79081e-69
NZ_CP011130.1|WP_036113117.1|6297410_6298466_-|two-pore-domain-potassium-channel-family-protein	gnl|CDD|369572	pfam07885, Ion_trans_2, Ion channel. This family includes the two membrane helix type ion channels found in bacteria.	1.85669e-09
NZ_CP011130.1|WP_036113304.1|6305764_6306847_+|cell-division-protein-ZapE	gnl|CDD|224402	COG1485, COG1485, Predicted ATPase [General function prediction only].	7.74235e-161
NZ_CP011130.1|WP_036113120.1|6299014_6299779_-|PspA/IM30-family-protein	gnl|CDD|281941	pfam04012, PspA_IM30, PspA/IM30 family. This family includes PspA a protein that suppresses sigma54-dependent transcription. The PspA protein, a negative regulator of the Escherichia coli phage shock psp operon, is produced when virulence factors are exported through secretins in many Gram-negative pathogenic bacteria and its homolog in plants, VIPP1, plays a critical role in thylakoid biogenesis, essential for photosynthesis. Activation of transcription by the enhancer-dependent bacterial sigma(54) containing RNA polymerase occurs through ATP hydrolysis-driven protein conformational changes enabled by activator proteins that belong to the large AAA(+) mechanochemical protein family. It has been shown that PspA directly and specifically acts upon and binds to the AAA(+) domain of the PspF transcription activator.	6.73658e-25
NZ_CP011130.1|WP_036113123.1|6299775_6300192_-|DUF2170-family-protein	gnl|CDD|378318	pfam09938, DUF2170, Uncharacterized protein conserved in bacteria (DUF2170). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.28193e-40

Protein sequences

>NZ_CP011130.1|WP_036113117.1|6297410_6298466_-|two-pore-domain-potassium-channel-family-protein
MIVIGKLFRSLRGHLRRISWGVVAAALVLHMTGTWLLLAWAGEDKLLGWDSFVYYYMTTASTIGYGDLSPGTPAGRWAAALFVMPGAIALFASVLAKTSAGLLNFWKRHQVGKMSYEDMHGHTVLIGWHGRETQRLVQLLLADTHTDDEGIVLIAEGLSENPLPEQIRFVAVESYADCNEYPRAAIAQAARVIVHTDHDDRSLAAVFALMAHKPGAHVVAHFESAAVAQLVRSHYPHVECTRPLHVDVIARAAQDAGSSLVAGEWLGAGGPTQFSLQVPADAAPVRAGRLAAAFRAQSALWIGYRDGRTAAPVLNPPDHDEIAAGTLLYYLADARIDSARVPWASLAAAAV
>NZ_CP011130.1|WP_036113114.1|6296617_6297289_-|DUF2491-family-protein
MGWLDGLFGGKKQQAPEPATLPFAHELPLGLRINGRVAFDTLPFRAHPQAWTLRLPEGHQGIPCYGYIDLRGGHALHRFYLDEDAYLQVSTASGQVEGIKAFVFQETVNPANQAEFKRFIHEHPHLGADRIDYAGRTWYREFGDQLGTGGKAPPVIYDEVLYRHDPPRRDDDLTHYAMLYRREVPELDREEFLLVTAEDYGPSEFVITYAIGIDLTTADLDIT
>NZ_CP011130.1|WP_036113111.1|6296145_6296553_-|DUF350-domain-containing-protein
MDAPITAHSFLNFLAYAGIGIGVLVLAALALVLITPHRELSLIREGNSAAATAFAGTLIGLALPLHSAISNSVSLIDAAIWGAVSVVVQAVAFLLARLVAPKLSQQITLNQTAAGIFSAGVSVSVGLINAAAMTP
>NZ_CP011130.1|WP_036113107.1|6295516_6296137_-|DUF1190-domain-containing-protein
MTVHDRNSKRSRQLRLVLMAVSVPAVLTGCGDDEPSGKVLTSREDCAAQTEISPAECEKAYQQALVEHEKLAPRFESEKECNDQFGACQPAPVAATASTTSHSYMPSMSGFLIGYALSQAMQPRGYYGIGGVSPLYRDYRSGGYLRPGGELVGKSSGTVYGKYGNTALPARAMTVSRAGFGSSAAARGGFGGSRSSGSSRGGSWGG
>NZ_CP011130.1|WP_057923308.1|6294234_6295428_-|glutathionylspermidine-synthase-family-protein
MKRILTTPRPDWREQAQSLGFHFHTIDGEAYWDESAYYAFGLRQIEDDIEQPTQELHDMSMALVDEVVGSEELLTRLAIPTDYWDWIAASWRQREPHLYGRMDLAYDGRGPAKLYELNYDTPTSLYEAAYFQWLWLEQAIARGALGEGSDQYNRIQELLIETFATLSREKRIATPVHFAAVEDSVEDQGTVRYLRDCAEQAGVDTLELSIEGIGLSKEGWFTDGDDRVIKTLFKLYPLEWMFVEEYGPKLAASQVQLIEPAWKAILSNKGVLPLLWERHRDHPNLLEAHFEDAAAQTAELPAGWVRKPLFSREGANIELVSASGERLRSDGPYQDGPTIRQAHHPLPRFDGDDGAANYPLIGSWVVADQAAGMGIREDASPITQDTSRFMPHAIVED
>NZ_CP011130.1|WP_057923307.1|6292193_6293837_-|M4-family-metallopeptidase
MSLHSNLPKRAVLSFAVVAALAAPVVHAADSGKALAMNQARGLIANHLDALQGNSDDSFNARDAIVDRDGTEHVRFDRTFRGLRVIGGDVVVKSQRGQLRSALLTLRSKQRPSLTPRISKDDAAVEAGARFGSRIEQVRGNEPVVYARGAKPVLAYEVTVQGEGNSRHSGLVTYYVDAASGKVLDVQDQIQTAAATGTGKSLYYGTMSISTDQKSATRFDLIDTTRGGGSVYDAKGAAVSNLFDILSTTSNATLMTDTDNIWGNNTTSDRATVGVDIHYGVGVTWDYYKNVHGRAGLRGDGVGIKSYAHTNFKTSSGTNSGANAAYVDLVKSMFYGDGDAARGIGPVVGIDVAGHEMTHGVTAATSKLAYSGDSGGLNEAASDIIGTLVEFYANNASDPGDYRIGEKMRTDGKAFRDMYNQASDGKSFNCYIAGGFDPALSDGAHNPHYTSGVGNLFFYFLAEGSVAPAGTGLNPAQMACNGDAGMTGIGRDKAGKIWYRALTAKFTSNTTYPQARAATLAAAGELYGNGSAEQNAVARAWSAVKVN
>NZ_CP011130.1|WP_148650672.1|6291556_6292066_+|hypothetical-protein
MRTIFCVVLCLLSGQSVAGGEIVPTDDPGSDCVAATIATRRSAANRTYDEAYCSVNKDPTAYRTCLKNAAANPTIAFFTDRCGDAEDGAYVSFNGQTHQVRRKSESPHRLVRYAGTYTGEGVSVRVVPGKLIERFVEDGEVLGVTYSVDVFITRGGETVKIAAIYDDRR
>NZ_CP011130.1|WP_057923305.1|6289564_6291223_-|M4-family-metallopeptidase
MTTRRFKQEGLYLAIAATLLMAPLAHAAEAGPAARDAATAQARGLIAGNAGLLRASAADSFEARDVVIDRDGTQHARFARSYQGLRVIGGDVVVTSRRGELKSAQLSLRSAQRPSLSARVIGKDQAAIEAGARFNGRVSKIHGNELVVYARGATPVLAYEVTVQGEETEQHSGFVTYYVNASDGRVLDVQDQLQTAAAIGTGKSFYYGDLSLPTDQKSATKFDLIDTTRGNGKVYDAKGAAISNLFDILGATLGATLFTDADNTWGNNTLSDRATVATDIHYGVGATWDYFKNVHGRLGLYNDNKGINSYAHTNFKTSTGGTTGVNAAYFALTKVMFYGDGDASRGYGPIVGIDVAGHEMSHGVNAATANLAYSGDAGGLNEANSDILGTLVEFYANHPNDPGDYRIGEIMRTGGLAFRDMYNQGADGKSFNCYIGGSGFDPNLAAGGIHDPHYTSGVANRMAYLAIEGAVTPAGTTLTPAQLVCNGDTGIVGIGRDKFGKIWYRALTTKFTSSTTYPQARAATLAAAAELYGAGSPEQTTIARAWSAASVN
>NZ_CP011130.1|WP_057923304.1|6288577_6289291_-|4'-phosphopantetheinyl-transferase-superfamily-protein
MDRNAFIHDAAPFDAQAHGQPLTGYACRFRLEAYDDALYPDHGLRLPPQLARAVAKRRGEFLAGRLCARRALARLGIASADIAIGPDREPLWPAGAIASISHAGDRAVCLASADPHVIGLGIDIESRIDARLAGEIRGVVVDAAEQAVIEAGFDDAVAGLAAAFSAKEALYKALYPQVRAFFGFEAMRLARVDEGRLRFLAAADLSPTVRAGQAFEVDIAFEDGGVRSIACCLRARG
>NZ_CP011130.1|WP_148650671.1|6286345_6288493_-|aminodeoxychorismate-synthase-component-I
MRCLLIDNYDSFTWNLADQIGRAFGQAPTVLRNDACGWEQLRADQDYDCIVVSPGPGSVEHEADFHVARQAIAHSALPLLGVCLGFQGIAYAEGGRIAHAPQPYHGRVSRLHHDGSELFAGLPASFEVVRYHSLIAAAPLPPALQATAHTDDGLIMALRHRRRPQWGVQFHPESILSEHGIDLIANFRDLVHRHHGRAFVSLAAATIEPPPAAPIAPPQALQLWCKPLDAKLDPETVFNALYAQQRNSFWLDSQDAVEERAACSFMGAVADEDLLAYRIADDDAALSSGHALLDRIERELAAGQVGEPILADADNALPFDFRGGFIGWLGYEMKALFDGDGSGNAGTPLPDALWMCVHRFLAFDHRRGRAWAIAIAAPHTAQAADAQRWLETVAAQAASTLAQPAPEPPPPPAPLDTLEVDMDLGHDDYLAAIEQCRRAIVDGESYQICLTNHFRFRARLDPLALYLRLRRGNAAPFGAYLRSGDHHVLSTSPERFLRVDRTGRIQTKPIKGTMRRSDDPRVDAQYARHLAESVKDRAENLMIVDLMRNDLNRVAVHATVEVPKLREVESYRTVHQLVSTVEAQLRPDTSLIDLLRATFPGGSISGAPKRRTMQIIDRLERSARGVYCGSIGYLGYNRVADLNIGIRTLSYDGDSVAFGAGGAITWLSDPQAEFQEVLLKAEAVLRPLWGFLARPDAGFAYELDGERLRLHRVAR
>NZ_CP011130.1|WP_036113120.1|6299014_6299779_-|PspA/IM30-family-protein
MSILQKILTLFRGTAHEAGQAVVDANALKILDQEIRDAGTELIRSKEELTKVMAQRQLQANRSKDRFAKKAEYETYIAGALRKGDEALAREVAERLAVVETDLKNDEQAINSYDASINQLKTAITATERKLARVKQQVDTVKATEAVQRAQTAVAARHSGATGKVTTALDSLERIQTRQAERGARLQAAAQLESESGDGDLNAKLANAGLLPESTSVENILERFREKPVQQLSHEPLSLPAVEVKETDKVERKE
>NZ_CP011130.1|WP_036113123.1|6299775_6300192_-|DUF2170-family-protein
MSRWTTQELLTRLGASFGAEYVEEVPTADGAIQVTLPDSGDLGITIALTDREIFVSTPLVEAGQVRDAAGFNEACLRLNPINPLSNLGLTTINERDVYIVFGEMAPDSTAEQIELEIRTLADNAIDAVEALKSYLVTA
>NZ_CP011130.1|WP_057923309.1|6300641_6301157_+|cytochrome-c5-family-protein
MRNYDLEFLKKFSMVIGFLMLVTLGLMIAAYFVHKQLPQEIDPRAAKRTENRIGPVGAVYAGATGAASQQAAVAAAAAKAASQVAYDGTLDGKVIFDNLCAGCHKSGAGGAPTLDASHWAARLPKGKDTLHKHALEGFTGSAGVMPPKGGNPALSAQQVAATVDWMLDNIK
>NZ_CP011130.1|WP_057923310.1|6301863_6303660_+|ExeM/NucH-family-extracellular-endonuclease
MTRFRPALAFAPCLLLAACATAPRVERAEGTLAIGAVQGHGAASALVGQTVTIECRVTLARAGADAAPGWVVQDGGDGDPASSDAIWVTGAAAASLASDQLVRITGRVREAAVDSGRRGPPRTLTAIDAERIEPLTSRAQRKALAAIAPVAIDAAPDWSRLEGMRVRIAAPLTLGERDPKTHTLSASFDGPLWQPGERAAPGSDAARAIASDNERRRLVLSGDATTLTAAAFAARSGSRLDAVDGIAWPVGGHAGIVLAAAPTLQPAPRPQPPQVDGDLRISAFNLENLFNGDGRGGGFPTPRGARTQAEYHAQLAKLVETIHTLNPDVAALMELENDGYGPDSTLADLVAALDRADAADGGAQDWRFAAPCKQPCAAGVKGPGDDQIRVGLIYRGQRVAARGLAATLQQGPFGPLARVPMAQAFTAIGAGKRPGPAFVVVANHFKSKGCGKNAAGLDKDQGDGASCWNAARTDSAQRLDAWLKTDPTGSRGELTMIVGDLNAHAQEQPLRALYAAGWLDAFAVAKVEAPYSYVYDGELGRLDHALLSPSLAARLRGAAEWHTNADEPEHAGYRDGGAGPWRSSDHDPVLLGFDLMPR
>NZ_CP011130.1|WP_057923311.1|6303898_6304597_+|alpha/beta-fold-hydrolase
MSTPAFPSDASTALSLPGPAGAIEMIVEAAEATPRPIVAIVCHPLPTEGGTMHNKVVTMTARALRECGAATVRFNFRGTGASQGEFDQGEGEGDDLRAVAAWVRATRPDAQLWLAGFSFGAYVSLRMADELQPKLLISIAPPAGRWDFDRIAPPSGYPWIVIQGEADEIVDPEAVYAWLDGLRQPPELVRMPDTSHFFHRRLIDLRGAIKHSVRPHLPPETAASPDSAADPA
>NZ_CP011130.1|WP_057923312.1|6304649_6305729_+|DUF1311-domain-containing-protein
MRHALSLALLSLCASLVATGWSGDAAAAGIACAKAASKNERAICADPVLGRRDGELAQAYRAALKASAYGGQLKKDQLAWIKERDRCDGQVRCLRMAYVERLTELQPAAIAGKFQWDGDWTRSDGGATLNLKSLGRDKYQIELQASSGANTGLLSGRARAVNDNEMVYKGKTGADGDNSRCELTFHRFHRQLQIEQQHTSNDCGAGLGVHFSGRYLPGLGEAVATTQWNLLDLGLLLKPEDDASLRRLLGDDYDLLVERLDVIDTRADQEGLDATVTNGYVRGLASDMRALLIQSADGGKFWVAIRAQDKQGKPELRYYSNDPAWTAKLPRTIDTWSDGYQEHPPVRLMSAGGRVLRSP
>NZ_CP011130.1|WP_036113304.1|6305764_6306847_+|cell-division-protein-ZapE
MTPSQAYAAGVARGDWSDDPAQHPALRELDRIHAGVLDPPSQSLFDRLRGKPREGVRGLYLWGGVGRGKTFLIDLFYEHLPIAEKRRTHFHRFMREVHAQLRNHAGESDPLAKIVREWRDQLRVLVLDEFFVIDIGDAMLLGRLLDRMFAEGVTLVTTSNTQPANLYADGLQRDRFKPAIELIGRHCETVLLDSAQDYRLRALTRSPVYRAPLDAQSDAWLAGRWKELAAGCASANGPLRIEGRDIPVRALADGHAWFDFAALCEGPRAASDYIEIATEYHTVLLGGIPRFPGGIHDDAARRFINLIDEFYDRHVNLVCTADEAPTGLYQGHRLAAAFERTASRLIEMQSAEYLALEHRG
>NZ_CP011130.1|WP_036113138.1|6307321_6307717_+|HU-family-DNA-binding-protein
MATKKPAAKKKAAPKAAPKAAAKTAAPKPIKEVLSKSALVAHLAETTGVVAKDIRSILGALEGAVHASINKKGAGAFTLPGLLKITAVSVPAKPKRKGINPFTKEEQWFAAKPATVKVKVRPLKKLKDAAA
>NZ_CP011130.1|WP_148650673.1|6308039_6308408_+|hypothetical-protein
MDPISLEELALLDVLQRIDQGQPLTRHSRALHDRLISTALVEVGLIVPGEEPGLQLTDAGVERCKSLRHRVAADTEALQVLREREEAGAPSPAQTDVARSGLTQIGRGDDADSVTIDLSQAG
>NZ_CP011130.1|WP_057923314.1|6308555_6309362_+|hypothetical-protein
MTPFDRHLTAWKLVPDGAPIHTHSSDLLPVRRDGEAAMLKIPRDAEEKFGALMMRWWDGDGAARVLAFDQDALLIERACGPRSLSHMARNGRDQDATRILCETINRLHAPRAAPPPSELAPLTQWFADLDTYARSHGGVLARCWQIAQELLAQPREVRPLHADIHHENVLDAGPGRGWIAIDPKRVIGERGYDFANLFTDPDADTALAPGQFERRLDDVVEYGRIERRRLLQWIVAFQGLSAAWFLSDEEEPAKEFAIIGMALAQLDR

Crispr_ID: NZ_CP011130_22

• CRISPR_ID: NZ_CP011130_22
• CRISPR_location: 6354150-6354276
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP011130_22

Consensus_repeat	Method
GAGAGTCGGGAATCGTAAATGCGGCCGCGCGGCGCTCTGGCT	CRISPRCasFinder

spacers of NZ_CP011130_22

>22.1|6354192|43|NZ_CP011130|CRISPRCasFinder
CCTGCGATTGCCGATTCCCAATGTCTGGGCGGGAATCGGGAGG

CRISPR arrays and Neighbor proteins around NZ_CP011130_22

CRISPR arrays

The CRISPR arrays of NZ_CP011130_22

>merge|NZ_CP011130|22|6354150-6354276|CRISPRCasFinder
GAGAGTCGGGAATCGTAAATGCGGCCGCGCGGCGCTCTGGCTCCTGCGATTGCCGATTCCCAATGTCTGGGCGGGAATCGGGAGGGAGAGTCGGGAATCGTAAAAGCGGCCGCGCGGCGCTCTGGCT

>NZ_CP011130|22|21|6354150-6354276|CRISPRCasFinder
GAGAGTCGGGAATCGTAAATGCGGCCGCGCGGCGCTCTGGCT	CCTGCGATTGCCGATTCCCAATGTCTGGGCGGGAATCGGGAGG
GAGAGTCGGGAATCGTAAAAGCGGCCGCGCGGCGCTCTGGCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011130.1|WP_046658546.1|6353669_6354029_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_036103255.1|6364348_6365167_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|237896
NZ_CP011130.1|WP_057923335.1|6349643_6350615_-|EamA-family-transporter	unknown	unknown	gnl|CDD|273359
NZ_CP011130.1|WP_187313309.1|6351941_6353042_+|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl|CDD|381093
NZ_CP011130.1|WP_046658543.1|6344900_6345299_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923339.1|6358381_6358840_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923334.1|6347831_6349622_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_148650683.1|6343974_6344232_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923333.1|6345991_6347749_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_082648832.1|6359090_6362225_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP011130.1|WP_057923337.1|6354313_6356860_-|ATP-dependent-helicase-HrpB	unknown	unknown	gnl|CDD|273901
NZ_CP011130.1|WP_057923342.1|6363672_6364212_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_082648833.1|6365163_6366192_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP011130.1|WP_036103258.1|6366577_6367324_+|ferredoxin--NADP-reductase	unknown	unknown	gnl|CDD|99792
NZ_CP011130.1|WP_148650684.1|6356929_6357361_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP011130.1|WP_057923336.1|6350736_6351690_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381307
NZ_CP011130.1|WP_046658549.1|6357530_6358325_+|TatD-family-hydrolase	unknown	unknown	gnl|CDD|182449
NZ_CP011130.1|WP_057923760.1|6343149_6343971_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|227135
NZ_CP011130.1|WP_057923761.1|6344302_6344836_+|pseudouridine-synthase	unknown	unknown	gnl|CDD|211334
NZ_CP011130.1|WP_057923341.1|6362689_6363556_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP011130.1|WP_057923337.1|6354313_6356860_-|ATP-dependent-helicase-HrpB	gnl|CDD|273901	TIGR01970, ATP-dependent_RNA_helicase_HrpB, ATP-dependent helicase HrpB. This model represents HrpB, one of two related but uncharacterized DEAH-box ATP-dependent helicases in many Proteobacteria, but also in a few species of other lineages. The member from Rhizobium meliloti has been designated HelO. HrpB is typically about 800 residues in length, while its paralog HrpA (TIGR01967), also uncharacterized, is about 1300 amino acids long. Related characterized eukarotic proteins are RNA helicases associated with pre-mRNA processing. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP011130.1|WP_082648833.1|6365163_6366192_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.92543e-94
NZ_CP011130.1|WP_057923335.1|6349643_6350615_-|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].	6.76831e-16
NZ_CP011130.1|WP_187313309.1|6351941_6353042_+|hybrid-sensor-histidine-kinase/response-regulator	gnl|CDD|381093	cd17538, REC_D1_PleD-like, first (D1) phosphoacceptor receiver (REC) domain of response regulator PleD and similar domains. PleD contains a REC domain (D1) with the phosphorylatable aspartate, a REC-like adaptor domain (D2), and the enzymatic diguanylate cyclase (DGC) domain, also called the GGDEF domain according to a conserved sequence motif, as its output domain. The GGDEF-containing PleD response regulators are global regulators of cell metabolism in some important human pathogens. This model describes D1 of PleD and similar domains. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.86933e-41
NZ_CP011130.1|WP_036103258.1|6366577_6367324_+|ferredoxin--NADP-reductase	gnl|CDD|99792	cd06195, FNR1, Ferredoxin-NADP+ (oxido)reductase is an FAD-containing enzyme that catalyzes the reversible electron transfer between NADP(H) and electron carrier proteins such as ferredoxin and flavodoxin. Isoforms of these flavoproteins (i.e. having a non-covalently bound FAD as a prosthetic group) are present in chloroplasts, mitochondria, and bacteria in which they participate in a wide variety of redox metabolic pathways. The C-terminal domain contains most of the NADP(H) binding residues and the N-terminal domain interacts non-covalently with the isoalloxazine rings of the flavin molecule which lies largely in a large gap betweed the two domains. Ferredoxin-NADP+ reductase first accepts one electron from reduced ferredoxin to form a flavin semiquinone intermediate. The enzyme then accepts a second electron to form FADH2 which then transfers two electrons and a proton to NADP+ to form NADPH.	3.56978e-72
NZ_CP011130.1|WP_057923336.1|6350736_6351690_-|aldo/keto-reductase	gnl|CDD|381307	cd19081, AKR_AKR9C1, AKR9C family of aldo-keto reductase (AKR). Haloferax volcanii aldo-keto reductase is a founding member of aldo-keto reductase family 9 member C1 (AKR9C1).	2.59275e-174
NZ_CP011130.1|WP_057923761.1|6344302_6344836_+|pseudouridine-synthase	gnl|CDD|211334	cd02566, PseudoU_synth_RluE, Pseudouridine synthase, Escherichia coli RluE. This group is comprised of bacterial proteins similar to E. coli RluE. Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil, psi). No cofactors are required. Escherichia coli RluE makes psi2457 in 23S RNA. psi2457 is not universally conserved.	1.76956e-90
NZ_CP011130.1|WP_036103255.1|6364348_6365167_-|ABC-transporter-permease	gnl|CDD|237896	PRK15066, PRK15066, inner membrane transport permease; Provisional.	7.401e-156
NZ_CP011130.1|WP_057923760.1|6343149_6343971_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|227135	COG4798, COG4798, Predicted methyltransferase [General function prediction only].	1.55383e-52
NZ_CP011130.1|WP_046658549.1|6357530_6358325_+|TatD-family-hydrolase	gnl|CDD|182449	PRK10425, PRK10425, 3'-5' ssDNA/RNA exonuclease TatD.	3.92222e-112
NZ_CP011130.1|WP_082648832.1|6359090_6362225_-|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	3.92104e-20

Protein sequences

>NZ_CP011130.1|WP_046658546.1|6353669_6354029_-|hypothetical-protein
MSKFESLPDRALELVHAISANLKEAAPKAGQWLETGAKFGALKTGARTAGGFIRRNPVVAVAAVAGAGLLWYAAARRKARLQSEEPIEGSARRVEARRANGQTSRRRTTRQASEESPNE
>NZ_CP011130.1|WP_187313309.1|6351941_6353042_+|hybrid-sensor-histidine-kinase/response-regulator
MSTPATSTGRILVVDDQAANLRVVTALLSRQGYEVVSASTGDEALRLYAESPPDLILLDVMMPGMDGFEVMSALRAGSPLRVPVVFVTAAHDRDLLLRAFDAGVVDYVTKPFLPEELLARVNAHVGLKLTRDRLERVAREREELVNLVAHDLKNPLTSVLFASDLLINHGCKPERVPRYLQMIHESADDALGYIRHYLESQAGTRERAEQNGRADLSETLDWLVRRYEMQLDARGIRVEIAPPPSGAAKVAMDPRVLRQVSENLVTNAMKYAPGSDLLLAARNSAPGFWQLIVADRGPGIPAARQRELFKPFVRLHDDEIDDGLSNGLGLSLAKQIVVNAGGQLWYESRKSGGSRFIIELPEASGE
>NZ_CP011130.1|WP_057923336.1|6350736_6351690_-|aldo/keto-reductase
MSLRPLGRSSLRVAPLAFGGNVFGWSADEATTFALLDGFVDAGFALVDTADMYSSWVPGNRGGESETLIGSWLAQGGGRRERVVIATKVAKWSQRPGLSPANIQAAAEDSLRRLRTEVIDLYQAHEDDPSVPLEDTLGAFARLIEQGKVRAIGASNYSAARLAQALDVAERHGLPRFETLQPHYNLYDREVFEAQLEPLVRERGIGVINYYALASGFLTGKYRSRADLGKSRARGGAVEKYLDARGLRILAALDEVAGAHGATPAQVALAWLIARPSITAPIASATSVAQLQELLAATRLTLAADEIATLDAASAEA
>NZ_CP011130.1|WP_057923335.1|6349643_6350615_-|EamA-family-transporter
MNAATTTAAAPVATTRRVGIALAASGAILFSAKAILAKLQYRYGVDSLQVLTLRMAFSLPLFALLGIRETRRARARQALPSRRDWGLIVILGVLGYYLSSLLDFWGLEYVPVSLERLILFLNPTIVLLIGLFAFKRKVAAKEWIALAVSYAGVVLVMVENLRVQGDHVLFGSALVLGAAVSYALYLAMSGELVKRLGSLQLVAYAMIVSTAAVMIHYLIARPPSALLGLPWQVYAWAAANAVFCTFLPVTFTMAAVARLGAGTAAQFSVIGPVSLVFLGAWVLGEPITAIQLIGTAVVLGGVVILSRPGANSVPITATPTAPK
>NZ_CP011130.1|WP_057923334.1|6347831_6349622_+|hypothetical-protein
MSGLRSITFGFVAAVCAASAYLLYPVPADSASGRVVAAADDGGFDLIPPTVADLYITARTQDSQGNNALLAVTYAANQALPASLPLQVGGRQATLVRDSQNPQRYTAVIAFDFDAFLAEQTRRQQLAPSKPWVPRFDGREHIGDAPWAFLDPAQLRSDIARQVAIRIPRDVLLGPPIAISAPRSLMVVHPLVVEDPTRTYDACTNTGNPNGAWTFNKLMTDMANQPVTGVDPSDFVAQWLLAHAGASTVNGYTVDGSPAFSQILSEWPRLSGGKLNLAKSPMRLLAIVNRVDLRTNSAYGGGSAGEGRFVFGVIRPMTGGGCQEVPLTVILEYGVPKLGCPAVRSYAQQWAGLSTLVLGSSGYNAALQALTDQFALANASPGKPNRSAINQVRTNEEPWHPFWDWRQREDQLITAGPWLRPATTKQTPDRSFNTTASASPRLPQYVNANAPAILAGTYRVPQIYAGTRFLGGDTVTEPYWQHNLIANNNARHKFSLNTCGACHGPETDTDFTHIAPRASGAQAALSSFLTGAPAGGTLDAPMTYTLPDPAVPTTLRSYGDLAFRQSHLSTLASSSCPSGGLFTELHFFPIAMSATH
>NZ_CP011130.1|WP_057923333.1|6345991_6347749_+|hypothetical-protein
MSTLRSLSLGIGAVVCVGTVSLLSPATDATAAGRVTAAAIDFEQAPPAVDAIHITSLGQQTGGNALLALTYSKGQDLPTQIPFNAGDTTVQLQQDPSNPQRYTALIPFDFDGFVREQENRQILAQSQELVPEFSGRELIGQATVQFLNPTTLRQQILAGTPILVPGPVLPWPAALVRPERSLMVTHPGVVEDPSRTFDACTGAGNPNGAWTFNRMMTNMANQPMTGVLPADFVENWMRTWGTSTSINTFPVNLRSQVITQVLNTWPRIASTGKLDLNRSPFRLLAIVNRIDMRGNSAYGGGNAGETRFVFGVLRRSGTTCVAAPFTVILEYAPNVNGCPAVRNLANQWGNLGTLSLGSATYNAALQAITDPVIAANASPRKPNGSAINQIRSNEFLQNPWELREFKILQGSPQLRIVPAAQTPHHSRNNTALLANYINTFNTQILNNTYIVPLSYLGTPFQSGSVINPSPQQVWKAPGILNNNGRNKFSVNTCDACHGAETQTTSFLHVAPRSPGAQSVLSRFLIGNGSLAAPTTFTMPDPVSGTPRTYGDLQRRQTDLATLQSSTCLSGSLFHEATRAVLTASH
>NZ_CP011130.1|WP_046658543.1|6344900_6345299_-|hypothetical-protein
MQKILLLIVLAAAAVFAYLQWFAKPAYSIPTIEQNPIPKHEFYLLWRETALTLCDGNEPGPTTLTPPKCREYVTDKHERCVAQVGAQTPPTISSKAESKRLARPYLDCVIPGHFCNGVEVRTPAEALRHCSS
>NZ_CP011130.1|WP_057923761.1|6344302_6344836_+|pseudouridine-synthase
MLIAFNKPFGVLCQFTDRSQPPRPTLAGFGLPPDVYAAGRLDHDSEGLLLLTDDGGLAHRLTDPRHKQPKTYWVQVEGDPGEEALQALRDGVELNDGRTLPARIERLDPPSLWPRDPPVRFRKTVPDAWLAITIHEGRNRQVRRMTAAVGLPTLRLVRVAIGPHRLDALQPGQWRPV
>NZ_CP011130.1|WP_148650683.1|6343974_6344232_+|hypothetical-protein
MRRPLARVVAALAAGALAAWAAGELAMSLIASYFMAEYGLSSVSIGASAIGYWKACVVAVWIVSPLAFCAAGGLVWRGSRPRRRD
>NZ_CP011130.1|WP_057923760.1|6343149_6343971_+|class-I-SAM-dependent-methyltransferase
MKPAAKPAEPKPTTKPATKPAGDVGSPSLRAAVAGSWRDPKNVARDGYRHPLETLTFFGAKPEQTIIEITPGGGWYSEILAPFLRERGKYVAAVVDPDTQSSDGARKYQTKAKATLEQKFAASPAQYDKVVIAAYDSFKPAFGPADSADLVLTFRNVHNWRSAGQAEVMFRGFYDVLKPGGTLGVVEHRAKGDVPADDKTGYVGQAQVIALAEAAGFKLEAKSEINANPRDTKDHPNGVWTLPPVNQHDAADDAKYQAIGESDRMTLRFRKPR
>NZ_CP011130.1|WP_057923337.1|6354313_6356860_-|ATP-dependent-helicase-HrpB
MTHAQFPIDALLPRIRDSLAAHPRLVLEAPPGAGKTTQVPPALLDAPWLQGRKIIVLEPRRVAARAAANFMARQRGESAGESVGYRIRFENKVSAATRIEVVTEGILTRMIQDDPSLEGVGALLFDEFHERHLTADLGLALALDVQASLREDLRIVVMSATLDGERLAQFLDAPRLSSAGRSYPVNVSHFPARREEKLEHQLKRAVEHALAQHPGDLLVFLPGQREIARADAALAGSEALRGIDVLSLHGELPVEQQSRVLQPDPDGRRRVVLATNVAESSVTLPGVRVVIDSGLAREPRYDPNSGFARLDVVAIAQASADQRAGRAGRVAEGWAYRLWPESQRLEPQRRPEIAQVELAGLMLELAAWGDAGLRFVDAPPSGALGAARELLLRLGALEGSEQTAPTITAFGKRMLALGTHPRLAAMLLAPSDPREKALACDLAALIEARDPLRSGGDALAARWQALAAFRAGRAPADASRSALATLDQAAKQWRRRLRVDIAPPASVPAHALGDLLLHAFPDRIAHQHPSDPYRYQLANGRSAKLFDDSAVYGEPWLVISELRDDPRDARILRAAPLDETRLQREFPRRFVSEDRVIWDAAARGIAAVRERRYDRIVLDSRPLAKPDPARYADALVDAVRQLGLDALPWTEGLRQWRARVRCLREWMPELAKGEHALPDLSDEGLLATLDEWLKPALRGKTRLDALDEAAFGDALRSLADWSWRQKLETLAPTRIAVPSGQERAIHYRFEAEHHDPHIGADPPVLAVKLQELFGLAETPRIADGRVPLTLHLLSPAGRPLQVTQDLRGFWERGYLEVRKEMKGRYPRHPWPDDPWTATATHRAKPRGT
>NZ_CP011130.1|WP_148650684.1|6356929_6357361_-|hypothetical-protein
MRSASPWLAVGLILMLSGGVFAMAMPAAAAEFPRQTFRGGNAGWGVVIGANKAGTLRYNLVAPARVGVSFGALSVVAKPRIGQYALQGPLTSGDRQDELIVMIAPAAAGAPCRDSAGRTHPYAVIANGGRAGAWYGCGDFGTD
>NZ_CP011130.1|WP_046658549.1|6357530_6358325_+|TatD-family-hydrolase
MQLIDIGANLTHDSFDPDRDAVLQRARDAGVTRMVITGASREHSPKALELARQHPGELFATAGVHPHHAIEYTAECDAEMRELLAHEQVVAVGECGLDYFRDFSPRPAQRRAFEMQLQNAVDTGKPLFLHQRDAHEDFMAMMKNFDGKLGAAVVHCFTGTREELFDYLDQDWHIGITGWLCDERRGLHLRELVKHIPAARLMIETDAPYLLPRTVKPAPSHRRNEPKYLAHIVEELARDRGEDAAVTAANTTATANAFFRLPPA
>NZ_CP011130.1|WP_057923339.1|6358381_6358840_-|hypothetical-protein
MRILFAAALALAAAFAAPCVSAQAITFPSPAFRGGNTDWKIKLTQSTTVVYELKVPQSAERLNGPLTHVKAAQPGQYQLLGVIGAEKSALTVKIAPVKLGETCKDNKGNIGGVYGPYTYAIMVVPAPAKPATGSKHKPWPKLWYGCGNFTLD
>NZ_CP011130.1|WP_082648832.1|6359090_6362225_-|TonB-dependent-receptor
MNRTHLRQACLRRRPLMLGILVAIATPAFAQQAPAAAEPETGAASKSPTDLDRMVVTGSRIRRAGFDTLEPATVVTKQYISDRGLTNVADALNEIPGFGAGITPEGNQSGFGTGVNFVNRFGLGSNRTLVLVNGRRYVSSSPTTLFGPAAPGVQVDLNAIPTAMVERIENVAIGGAPTYGSDAIAGVVNVILRKNYEGVEFGASYGVTGEGDNERYNVWALVGAGFDEGRGNVTFSLSYDDVKGVLQKERDFFADGYFNTTNPLASQMATLFPGRTPANDGRYNPNIPFNTGSNDGIPNGVLIKNRHIWSTPFGGLISPTTGAFKPGSGNLIANGFGPGGNTVLGFDRSGNLVPYNQGTPFSQTDASGGDGLSLVEAGQITSDLKRMSFNTTARWGLTDRVDVFLEGSFYSAESTELADQWVFNAPLFGGLSAMIRFPSNYALLTDQARTTLQGLGVAAFNLSRASRDLVTNNGSGTTEIGRVVVGLEGDFDLGERTFYWETSANYGRSDSRAYGTSLVQQNFINALNVTRNAQGQVVCSPTPIAGLVIPGGGRPIADPNCVPLDLFGEGRPSAAARNYVTTRTASQALQEQKIFNANISSTLFDLWSGPIQYNVGFEYRKESGLFDPGAFLTQGLGRSVPITPLQGEYSTREWFGEFVVPLVNPEANVPLLKKLEVVGKYRQVDNSINGKFDTYTYGLQWKPFEDLEIRGNFTRSLRSPAITEAFLPQATSFQFVTNDPCDGRFINAGGARQAQRTANCQAFLNYYGYGPGTPFTSTASGASIQGVSGGNPNLKNESADSYTYGFTWAPSFLEGLTFAADYYNIKITDVISNLTAAEIARACFDADDFDAGNIPNANAFCSKITRNAPGGPPNTAGQATTFVSGFVNGKYFNMEAYSAELAYRFKTERLGNFAFGVTGYFPVDLTVDNTGVSPDQAVGEIGTSKRQYQFSGAWEKGRFGVNLSANYLSRAQFDVLNTRETRDILSVDSYWLVNGGMRYRFNDRAQVRVAVTNLFDKDPPFPAIGIGTYDLLGRRYNVAFEWKY
>NZ_CP011130.1|WP_057923341.1|6362689_6363556_+|hypothetical-protein
MSDLASPVRSPALVPLALAANLLVFSAAFVLIGLLTAANAQPEFSGLVQAVEWLCSIGLLIGFVLVVGCMLSDRHGAPRRPWATVLAALVLIFGLGVGWAMLQGQVLNGLRSSYSVQQLLAWTAGIAALKVVAINLVALPIAWRLGGRGTTPVAWRGWHRRVIGALAGGFLCAGLALLLQNLAAAYTSLGHGEQRVGMSVVALAVGLIQALMILALPVRRGSGALPALLSALLTPLLIVAASLALLAVNSNSWGMTSLIAVVLLILLLAPILSWLLLRWLHGRSYRAD
>NZ_CP011130.1|WP_057923342.1|6363672_6364212_-|hypothetical-protein
MRLMPLAAILTVAVLAACSKPPVADPPAVDANKAVTADTAAPAADPNPAAPADQPMGKIGADQVGKVSPVPAFKGFGEHWSIDIHATGEMNHQVELTWGSGGEKASGSARYNGQPADASSSLIVLSGELATKQGAKPMTIEIKAGECVDDGDNKHMHSVQVHVDGMDALTGGCGDLAVY
>NZ_CP011130.1|WP_036103255.1|6364348_6365167_-|ABC-transporter-permease
MSQILPVQPANTVEPTAARRNLVALGTIVRREVARILRIWGQTLVPPAITMTLYFLIFGGLIGSRIGDMGGYTYMEFIVPGLVMMSVIQNSYGNISSSFFGAKFGRHVEELLVSPMPNWVILWGYVAGAVLRGLMVGAIVLMIAMCFTAVRIPHPLVTLTTVLLGATIFSLAGFINAVYAKKFDDVAIVPTFILTPLTYLGGVFYSVKLLPAWAEAATHANPIFYMVNAFRYGLLGSSDVPLPMAYGLMIAFVVALSSLALWLLKRGVGLRS
>NZ_CP011130.1|WP_082648833.1|6365163_6366192_-|ABC-transporter-ATP-binding-protein
MTQPTAPATGPSSATAGLPAAAPSASVPALRVRDLRKTYDNKVQALKGVSLDVAEGDFFALLGPNGAGKSTLIGIVSSLVNLSEGAVEIFGTDLIRHRDQAMRLIGLVPQELNFNMFEKPLDILVNYAGFYGVPRAVALVRAEEELKRAQLWEKANMMSRTLSGGMKRRLMIARAMMTRPRLLILDEPTAGVDIEIRRGMWKTLREINAAGTTIILTTHYLEEAEHLCRNLAIIDQGRIVQQGPMKTLLAMLDVEGFLFDIDGTLPAALPSIEGVTMLASDDHTLDVDMPRAMDLNRIFAALGQAGIRVRSMRTKSNRLEELFVRMINQPIDSSAASTETAA
>NZ_CP011130.1|WP_036103258.1|6366577_6367324_+|ferredoxin--NADP-reductase
MKQFPLKLVSRRMLAPTVGHYVFLRDDGEPLDYIPGQFIQVHFQYADGTSTKRSYSLATIHDHALGAGETVEIAVSYVPGGAATALFEGLNEGDPILASGPFGRFCLMPADANRRYLLIGTGTGVTPYRAMLPQLETLIRERGIEVVLLFGARTPDELLYGDEFRAFAEREPNFRFIPCFSRELPADPHPDVRQGYVQQFLAEFSPNPDGDIAYLCGNPNMVDSCFEALKEYGLPVPHIRREKYVSSK

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP011130_2	2.1|162053|25|NZ_CP011130|CRISPRCasFinder	162053-162077	25	NZ_CP011130.1	555857-555881	0	1.0
NZ_CP011130_17	17.7|5671409|18|NZ_CP011130|CRISPRCasFinder	5671409-5671426	18	NZ_CP011130.1	5668919-5668936	0	1.0
NZ_CP011130_3	3.1|178825|25|NZ_CP011130|CRISPRCasFinder	178825-178849	25	NZ_CP011130.1	116035-116059	1	0.96
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	18979-19004	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	178739-178764	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1933085-1933110	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2046489-2046514	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2451069-2451094	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2465139-2465164	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2515668-2515693	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2704490-2704515	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3187212-3187237	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3520695-3520720	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3675797-3675822	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3852517-3852542	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4766044-4766069	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	19184-19209	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	178853-178878	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	381018-381043	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	540627-540652	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2280830-2280855	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2307457-2307482	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3638477-3638502	1	0.962
NZ_CP011130_17	17.1|5671073|18|NZ_CP011130|CRISPRCasFinder	5671073-5671090	18	NZ_CP011130.1	2767976-2767993	1	0.944
NZ_CP011130_17	17.1|5671073|18|NZ_CP011130|CRISPRCasFinder	5671073-5671090	18	NZ_CP011130.1	2861061-2861078	1	0.944
NZ_CP011130_17	17.1|5671073|18|NZ_CP011130|CRISPRCasFinder	5671073-5671090	18	NZ_CP011130.1	5670509-5670526	1	0.944
NZ_CP011130_18	18.1|5671733|18|NZ_CP011130|CRISPRCasFinder	5671733-5671750	18	NZ_CP011130.1	2767976-2767993	1	0.944
NZ_CP011130_18	18.1|5671733|18|NZ_CP011130|CRISPRCasFinder	5671733-5671750	18	NZ_CP011130.1	2861061-2861078	1	0.944
NZ_CP011130_18	18.1|5671733|18|NZ_CP011130|CRISPRCasFinder	5671733-5671750	18	NZ_CP011130.1	5670509-5670526	1	0.944
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP011130.1	2114913-2114938	1	0.962
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	NZ_CP011130.1	4594844-4594868	2	0.92
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	NZ_CP011130.1	779891-779915	2	0.92
NZ_CP011130_2	2.1|162053|25|NZ_CP011130|CRISPRCasFinder	162053-162077	25	NZ_CP011130.1	266063-266087	2	0.92
NZ_CP011130_3	3.1|178825|25|NZ_CP011130|CRISPRCasFinder	178825-178849	25	NZ_CP011130.1	265984-266008	2	0.92
NZ_CP011130_3	3.1|178825|25|NZ_CP011130|CRISPRCasFinder	178825-178849	25	NZ_CP011130.1	2657374-2657398	2	0.92
NZ_CP011130_3	3.1|178825|25|NZ_CP011130|CRISPRCasFinder	178825-178849	25	NZ_CP011130.1	4774301-4774325	2	0.92
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	19030-19055	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	779915-779940	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	828643-828668	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1131256-1131281	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1131425-1131450	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1465114-1465139	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1589183-1589208	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1624172-1624197	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1915125-1915150	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1937821-1937846	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1984602-1984627	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2120133-2120158	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2516116-2516141	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2720617-2720642	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2897617-2897642	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	3165010-3165035	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	5170282-5170307	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	26020-26045	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	162138-162163	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	853292-853317	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	985158-985183	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	1131343-1131368	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2140331-2140356	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2570383-2570408	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2838048-2838073	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2891146-2891171	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	2897900-2897925	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4042003-4042028	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4126932-4126957	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4480468-4480493	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4594687-4594712	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	4646115-4646140	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	5170192-5170217	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	5712326-5712351	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	5723605-5723630	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP011130.1	5809691-5809716	2	0.923

1. spacer 2.1|162053|25|NZ_CP011130|CRISPRCasFinder matches to position: 555857-555881, mismatch: 0, identity: 1.0

agacttcagcgccattccaccagaa	CRISPR spacer
agacttcagcgccattccaccagaa	Protospacer
*************************

2. spacer 17.7|5671409|18|NZ_CP011130|CRISPRCasFinder matches to position: 5668919-5668936, mismatch: 0, identity: 1.0

gaggctgccgttgccgag	CRISPR spacer
gaggctgccgttgccgag	Protospacer
******************

3. spacer 3.1|178825|25|NZ_CP011130|CRISPRCasFinder matches to position: 116035-116059, mismatch: 1, identity: 0.96

ttctggtgagatgtcgctgaagtct	CRISPR spacer
ttctggtgagatgacgctgaagtct	Protospacer
************* ***********

4. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 18979-19004, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

5. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 178739-178764, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

6. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1933085-1933110, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

7. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2046489-2046514, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

8. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2451069-2451094, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

9. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2465139-2465164, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

10. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2515668-2515693, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

11. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2704490-2704515, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

12. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3187212-3187237, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

13. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3520695-3520720, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

14. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3675797-3675822, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

15. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3852517-3852542, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

16. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4766044-4766069, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

17. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 19184-19209, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

18. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 178853-178878, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

19. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 381018-381043, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

20. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 540627-540652, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

21. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2280830-2280855, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

22. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2307457-2307482, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

23. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3638477-3638502, mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacga	Protospacer
*********** **************

24. spacer 17.1|5671073|18|NZ_CP011130|CRISPRCasFinder matches to position: 2767976-2767993, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccgccgccgat	Protospacer
***********.******

25. spacer 17.1|5671073|18|NZ_CP011130|CRISPRCasFinder matches to position: 2861061-2861078, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccggtgccgat	Protospacer
********** *******

26. spacer 17.1|5671073|18|NZ_CP011130|CRISPRCasFinder matches to position: 5670509-5670526, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccgttgccgat	Protospacer
**********.*******

27. spacer 18.1|5671733|18|NZ_CP011130|CRISPRCasFinder matches to position: 2767976-2767993, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccgccgccgat	Protospacer
***********.******

28. spacer 18.1|5671733|18|NZ_CP011130|CRISPRCasFinder matches to position: 2861061-2861078, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccggtgccgat	Protospacer
********** *******

29. spacer 18.1|5671733|18|NZ_CP011130|CRISPRCasFinder matches to position: 5670509-5670526, mismatch: 1, identity: 0.944

ggtgttgccgctgccgat	CRISPR spacer
ggtgttgccgttgccgat	Protospacer
**********.*******

30. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to position: 2114913-2114938, mismatch: 1, identity: 0.962

cggcgccgcacttgccctcgccgcac	CRISPR spacer
cggcgccgcacttgccttcgccgcac	Protospacer
****************.*********

31. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to position: 4594844-4594868, mismatch: 2, identity: 0.92

agtcttcagcgtcatctctccagat	CRISPR spacer
aggcttcagcgtcatctctccggat	Protospacer
** ******************.***

32. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to position: 779891-779915, mismatch: 2, identity: 0.92

agtcttcagcgtcatctctccagat	CRISPR spacer
agccttcagcgtcatctctcccgat	Protospacer
**.****************** ***

33. spacer 2.1|162053|25|NZ_CP011130|CRISPRCasFinder matches to position: 266063-266087, mismatch: 2, identity: 0.92

agacttcagcgccattccaccagaa	CRISPR spacer
agacttcagcgccatccctccagaa	Protospacer
***************.** ******

34. spacer 3.1|178825|25|NZ_CP011130|CRISPRCasFinder matches to position: 265984-266008, mismatch: 2, identity: 0.92

ttctggtgagatgtcgctgaagtct	CRISPR spacer
ttctggagagatggcgctgaagtct	Protospacer
****** ****** ***********

35. spacer 3.1|178825|25|NZ_CP011130|CRISPRCasFinder matches to position: 2657374-2657398, mismatch: 2, identity: 0.92

ttctggtgagatgtcgctgaagtct	CRISPR spacer
ttctggtgagatagcgctgaagtct	Protospacer
************. ***********

36. spacer 3.1|178825|25|NZ_CP011130|CRISPRCasFinder matches to position: 4774301-4774325, mismatch: 2, identity: 0.92

ttctggtgagatgtcgctgaagtct	CRISPR spacer
ttctggtgagatgacgccgaagtct	Protospacer
************* ***.*******

37. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 19030-19055, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

38. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 779915-779940, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

39. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 828643-828668, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

40. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1131256-1131281, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

41. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1131425-1131450, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

42. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1465114-1465139, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

43. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1589183-1589208, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

44. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1624172-1624197, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

45. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1915125-1915150, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

46. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1937821-1937846, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

47. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1984602-1984627, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

48. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2120133-2120158, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

49. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2516116-2516141, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

50. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2720617-2720642, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

51. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2897617-2897642, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

52. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 3165010-3165035, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

53. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 5170282-5170307, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgcctgcgcggggatgacga	Protospacer
***.**************.*******

54. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 26020-26045, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacga	Protospacer
*********.* **************

55. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 162138-162163, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacga	Protospacer
*********.* **************

56. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 853292-853317, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgccttcgcgggaatgacga	Protospacer
***.******* **************

57. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 985158-985183, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

58. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 1131343-1131368, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacga	Protospacer
*********.* **************

59. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2140331-2140356, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

60. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2570383-2570408, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

61. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2838048-2838073, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

62. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2891146-2891171, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

63. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 2897900-2897925, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgcctgcgcggggatgacga	Protospacer
***.**************.*******

64. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4042003-4042028, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

65. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4126932-4126957, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccaccttcgcgggaatgacga	Protospacer
*******.*** **************

66. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4480468-4480493, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

67. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4594687-4594712, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacga	Protospacer
*********.* **************

68. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 4646115-4646140, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

69. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 5170192-5170217, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

70. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 5712326-5712351, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

71. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 5723605-5723630, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

72. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to position: 5809691-5809716, mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcgttcgcgggaatgacga	Protospacer
********* * **************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	748041-748066	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016108	Methylomicrobium alcaliphilum 20Z plasmid MEALZ_p, complete sequence	1776-1801	1	0.962
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP019045	Halioglobus pacificus strain RR3-57 plasmid pRR3-57, complete sequence	140526-140551	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	107809-107834	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	161436-161461	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	473745-473770	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	85917-85942	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	456119-456144	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	84059-84084	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	101878-101903	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	468489-468514	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP016453	Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence	339483-339508	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP054615	Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence	306839-306864	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	624496-624521	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	58018-58043	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	365563-365588	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	624557-624582	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	861517-861542	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1328784-1328809	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1332021-1332046	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	1011614-1011639	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	13254-13279	2	0.923
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	1624687-1624712	2	0.923
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP013054	Sinorhizobium americanum CCGM7 plasmid C, complete sequence	314371-314399	3	0.897
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	562230-562255	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	12930-12955	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	347830-347855	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	322941-322966	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	331559-331584	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	352495-352520	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	428160-428185	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	715171-715196	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	731071-731096	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	956863-956888	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	1396039-1396064	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	956935-956960	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP038636	Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence	357881-357906	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	181824-181849	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	781061-781086	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	40421-40446	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	40482-40507	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134418	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9	115086-115111	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	622590-622615	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	1007268-1007293	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134427	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 18	37622-37647	3	0.885
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	191836-191861	3	0.885
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	NZ_CP042825	Rhizobium sp. WL3 plasmid unnamed2, complete sequence	575923-575947	4	0.84
NZ_CP011130_2	2.1|162053|25|NZ_CP011130|CRISPRCasFinder	162053-162077	25	MN497415	Vibrio phage vB_VhaM_VH-8, complete genome	78547-78571	4	0.84
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	868303-868331	4	0.862
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	747980-748005	4	0.846
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP016453	Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence	74434-74459	4	0.846
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	1735591-1735616	4	0.846
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134418	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9	5843-5868	4	0.846
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134418	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9	115149-115174	4	0.846
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134417	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 8	81993-82018	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP010024	Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence	27928-27953	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP015737	Shinella sp. HZN7 plasmid pShin-01, complete sequence	348482-348507	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1648513-1648538	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1624975-1625000	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	MF140427	Arthrobacter phage Shrooms, complete genome	29656-29681	4	0.846
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	980835-980860	4	0.846
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	NZ_CP006990	Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence	708764-708788	5	0.8
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	NZ_CP021127	Rhizobium sp. Kim5 plasmid pRetKim5c, complete sequence	635954-635978	5	0.8
NZ_CP011130_1	1.1|116088|25|NZ_CP011130|CRISPRCasFinder	116088-116112	25	CP007644	Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence	691412-691436	5	0.8
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP023549	Rhodobacter sp. CZR27 plasmid unnamed1, complete sequence	834266-834297	5	0.844
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_001381	Mycobacterium fortuitum plasmid pAL5000, complete sequence	4056-4087	5	0.844
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP039909	Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence	353278-353306	5	0.828
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP011248	Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence	76863-76891	5	0.828
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP032919	Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence	76624-76652	5	0.828
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP033029	Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence	76708-76736	5	0.828
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022991	Paraburkholderia aromaticivorans strain BN5 plasmid pBN1, complete sequence	334623-334651	5	0.828
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NC_009427	Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence	82757-82785	5	0.828
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	643753-643781	5	0.828
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	1529179-1529207	5	0.828
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP013635	Rhizobium sp. N324 plasmid pRspN324e, complete sequence	649925-649953	5	0.828
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP030763	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed3, complete sequence	96602-96628	5	0.815
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP012886	Mycobacterium chimaera strain AH16 plasmid unnamed1, complete sequence	238346-238372	5	0.815
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP016453	Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence	339549-339574	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP054615	Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence	306908-306933	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	425130-425155	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134417	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 8	104888-104913	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	66020-66045	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	143210-143235	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	117363-117388	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	137671-137696	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	173245-173270	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	732488-732513	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	117483-117508	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	117488-117513	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	118632-118657	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	115006-115031	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	115317-115342	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	513983-514008	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1819021-1819046	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134428	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 19	45940-45965	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	295459-295484	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134420	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 11	112889-112914	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	1960242-1960267	5	0.808
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	1960242-1960267	5	0.808
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	CP009870	Pantoea sp. PSNIH2 plasmid pPSP-b98, complete sequence	12580-12605	5	0.808
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	166131-166156	5	0.808
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	562067-562092	5	0.808
NZ_CP011130_20	20.1|6263266|26|NZ_CP011130|CRISPRCasFinder	6263266-6263291	26	NZ_CP004394	Celeribacter indicus strain P73 plasmid pP73A, complete sequence	79462-79487	5	0.808
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP017304	Rhodococcus sp. YL-1 plasmid pYLL2 sequence	91966-91997	6	0.812
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP017664	Cronobacter sp. JZ38 plasmid unnamed2, complete sequence	139350-139381	6	0.812
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP048283	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248c, complete sequence	258720-258748	6	0.793
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP021802	Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence	1647755-1647783	6	0.793
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	441814-441842	6	0.793
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	23683-23711	6	0.793
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP035502	Sphingosinicella sp. BN140058 plasmid p1, complete sequence	28509-28537	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013524	Rhizobium phaseoli strain R744 plasmid pRphaR744b, complete sequence	172298-172326	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013559	Rhizobium phaseoli strain N841 plasmid pRphaN841b, complete sequence	183145-183173	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013576	Rhizobium phaseoli strain N671 plasmid pRphaN671b, complete sequence	183533-183561	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013548	Rhizobium phaseoli strain R611 plasmid pRetR611a, complete sequence	183531-183559	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013528	Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence	181690-181718	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013533	Rhizobium phaseoli strain R650 plasmid pRphaR650a, complete sequence	183531-183559	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013543	Rhizobium phaseoli strain R620 plasmid pRphaR620a, complete sequence	186943-186971	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	286852-286880	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013581	Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence	181693-181721	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP013570	Rhizobium phaseoli strain N771 plasmid pRphaN771b, complete sequence	183533-183561	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP020471	Rhodobacter blasticus strain 28/5 plasmid pRsa, complete sequence	145900-145928	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	CP021183	Sphingomonas wittichii DC-6 plasmid pDC02, complete sequence	96018-96046	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	56541-56569	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	344036-344064	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	336714-336742	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP044217	Mesorhizobium sp. NIBRBAC000500504 plasmid unnamed, complete sequence	164077-164105	6	0.793
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	711893-711921	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	1221675-1221703	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	799730-799758	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP049249	Rhizobium rhizoryzae strain DSM 29514 plasmid unnamed3, complete sequence	1030337-1030365	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	38431-38459	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	1449535-1449563	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_LR594690	Variovorax sp. WDL1 plasmid 2	38431-38459	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_HG938356	Neorhizobium galegae bv. officinalis bv. officinalis str. HAMBI 1141 plasmid pHAMBI1141a, complete sequence	1362841-1362869	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	38431-38459	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	596316-596344	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	338562-338590	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP024314	Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence	1091304-1091332	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	307377-307405	6	0.793
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP041605	Streptomyces sp. S1D4-14 plasmid pS1D4-14.1, complete sequence	29925-29953	6	0.793
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022999	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence	305497-305523	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1673639-1673665	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1456746-1456772	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1001857-1001883	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	964128-964154	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	832444-832470	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1062374-1062400	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1609478-1609504	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	879265-879291	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP047174	Rathayibacter sp. VKM Ac-2760 plasmid unnamed1, complete sequence	128079-128105	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1037146-1037172	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	180678-180704	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1056249-1056275	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	1046841-1046867	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1231479-1231505	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	839595-839621	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1384639-1384665	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	957279-957305	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1657859-1657885	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	70026-70052	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	1446621-1446647	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1044897-1044923	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	760929-760955	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	969692-969718	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	871748-871774	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	831559-831585	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	966395-966421	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	1202691-1202717	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	832437-832463	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	832456-832482	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	832428-832454	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	120981-121007	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	964559-964585	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1022966-1022992	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1044886-1044912	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	1202658-1202684	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1051818-1051844	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1079380-1079406	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	1201463-1201489	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	1056275-1056301	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	929831-929857	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1051818-1051844	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1079380-1079406	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	1201500-1201526	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1051818-1051844	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	929854-929880	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1051822-1051848	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1079380-1079406	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1079380-1079406	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1079380-1079406	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	1201500-1201526	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	997912-997938	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	1201489-1201515	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	929854-929880	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	968865-968891	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	949546-949572	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	997493-997519	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1043643-1043669	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1105785-1105811	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	1201489-1201515	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	929854-929880	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1051817-1051843	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1129806-1129832	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	1202656-1202682	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	929854-929880	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	929854-929880	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	1201500-1201526	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1079381-1079407	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	984103-984129	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	1201511-1201537	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	1201489-1201515	6	0.778
NZ_CP011130_10	10.2|3461867|27|NZ_CP011130|CRISPRCasFinder	3461867-3461893	27	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	984103-984129	6	0.778
NZ_CP011130_16	16.1|5199383|26|NZ_CP011130|CRISPRCasFinder	5199383-5199408	26	NZ_LR134429	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 20	29505-29530	6	0.769
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	MN855768	Siphoviridae sp. isolate 183, complete genome	9623-9651	6	0.793
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	1048570-1048601	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	794336-794367	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	1552029-1552060	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP026308	Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence	1551973-1552004	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	1039584-1039615	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP013381	Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence	236124-236155	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP009547	Burkholderia sp. 2002721687 plasmid pBTU, complete sequence	186847-186878	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_LR134451	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence	133175-133206	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_012725	Burkholderia glumae BGR1 plasmid bglu_4p, complete sequence	70583-70614	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	32122-32153	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP035902	Burkholderia glumae strain 257sh-1 plasmid plas1, complete sequence	112894-112925	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP052865	Burkholderia glumae strain HN1 plasmid pBGHN1-1, complete sequence	83235-83266	7	0.781
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	229312-229343	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MF324914	Mycobacterium phage Krueger, complete genome	15849-15880	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN234223	Mycobacterium phage Philly, complete genome	31097-31128	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KP027207	Mycobacterium phage Chandler, complete genome	32026-32057	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN096360	Mycobacterium phage Rita1961, complete genome	31230-31261	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MG839014	Mycobacterium phage RagingRooster, complete genome	31247-31278	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KJ194581	Mycobacterium phage Audrey, complete genome	31243-31274	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KR080203	Mycobacterium phage OrangeOswald, complete genome	31246-31277	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MH513976	Mycobacterium phage Morty007, complete genome	32025-32056	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MH051265	Mycobacterium phage Yahalom, complete genome	31256-31287	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MH316565	Mycobacterium phage Mortcellus, complete genome	31881-31912	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MT310871	Mycobacterium phage Jackstina, complete genome	31166-31197	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MK359357	Mycobacterium phage RomaT, complete genome	32020-32051	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	JF704095	Mycobacterium phage Daisy, complete sequence	31270-31301	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	EU816589	Mycobacterium phage Phaedrus, complete genome	31162-31193	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN096359	Mycobacterium phage Obutu, complete genome	31229-31260	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MK061414	Mycobacterium phage Marley1013, complete genome	32025-32056	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MT952851	Mycobacterium phage Gervas, complete genome	31224-31255	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MG925353	Mycobacterium phage Nozo, complete genome	32005-32036	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KJ194584	Mycobacterium phage Heathcliff, complete genome	31208-31239	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN444872	Mycobacterium phage SynergyX, complete genome	31247-31278	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KY945355	Mycobacterium phage Shandong1, complete genome	23697-23728	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MH576977	Mycobacterium phage Tydolla, complete genome	31981-32012	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MG925338	Mycobacterium phage ChaChing, complete genome	31258-31289	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_023742	Mycobacterium phage Akoma, complete genome	31247-31278	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MG920059	Mycobacterium phage Baloo, complete genome	31246-31277	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_023686	Mycobacterium phage Gadjet, complete genome	31253-31284	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KR080205	Mycobacterium phage Corofin, complete genome	31268-31299	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_041965	Mycobacterium phage Athena, complete genome	31994-32025	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	DQ398049	Mycobacterium phage Pipefish, complete genome	32638-32669	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	KF493879	Mycobacterium phage Bernardo, complete genome	31333-31364	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MT310892	Mycobacterium phage Compostia, complete genome	31673-31704	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	JN699018	Mycobacterium phage Kamiyu, complete genome	31212-31243	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_012027	Mycobacterium phage Phlyer, complete genome	31981-32012	7	0.781
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN444873	Mycobacterium phage Abinghost, complete genome	31243-31274	7	0.781
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	975425-975453	7	0.759
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NC_007950	Polaromonas sp. JS666 plasmid 2, complete sequence	7773-7801	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	44826-44854	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032328	Azospirillum brasilense strain MTCC4035 plasmid p7, complete sequence	776-804	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032328	Azospirillum brasilense strain MTCC4035 plasmid p7, complete sequence	148092-148120	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	382602-382630	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032685	Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence	274410-274438	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP032690	Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence	274410-274438	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP017750	Cupriavidus sp. USMAA2-4 plasmid unnamed1, complete sequence	192085-192113	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022999	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence	744864-744892	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	243117-243145	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	1130098-1130126	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NC_010492	Arthrobacter sp. Chr15 plasmid pChr15, complete sequence	17711-17739	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP048426	Rhizobium daejeonense strain KACC 13094 plasmid unnamed3, complete sequence	41204-41232	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	1031127-1031155	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	1031116-1031144	7	0.759
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	201916-201944	7	0.759
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	192620-192648	7	0.759
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	556250-556278	7	0.759
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	667868-667896	7	0.759
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP003988	Streptomyces sp. 769 plasmid pSGZL, complete sequence	181736-181764	7	0.759
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	MN657148	Polaromonas sp. strain ANT_J29B plasmid pA29BJ2, complete sequence	35077-35105	7	0.759
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022775	Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence	1877493-1877525	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	1968145-1968177	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	1776104-1776136	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP023017	Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence	1846299-1846331	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	1775124-1775156	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	1871470-1871502	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	1871472-1871504	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	1776114-1776146	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	1775498-1775530	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	1776084-1776116	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022764	Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence	1877683-1877715	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022797	Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence	1877680-1877712	7	0.788
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP022758	Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence	1877645-1877677	7	0.788
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP007214	Burkholderia plantarii strain ATCC 43733 plasmid bpln_1p, complete sequence	71264-71295	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	301827-301858	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP031358	Erythrobacter aureus strain YH-07 plasmid unnamed, complete sequence	194161-194192	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	399138-399169	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_013193	Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence	93884-93915	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	MH727545	Mycobacterium phage DismalStressor, complete genome	43782-43813	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	KJ510412	Mycobacterium phage ZoeJ, complete genome	43153-43184	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_026598	Mycobacterium phage Milly, complete genome	43755-43786	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	MH834601	Mycobacterium phage BoostSeason, complete genome	43360-43391	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	KX688047	Mycobacterium phage Marcoliusprime, complete genome	43782-43813	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_028759	Mycobacterium phage Mufasa, complete genome	43345-43376	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	MF140408	Mycobacterium phage DismalFunk, complete genome	43782-43813	8	0.75
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	MF140411	Mycobacterium phage Findley, complete genome	43775-43806	8	0.75
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	MN945901	Mycobacterium phage Ximenita, complete genome	16039-16070	8	0.75
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP017563	Paraburkholderia sprentiae WSM5005 plasmid pl1WSM5005, complete sequence	796212-796243	8	0.75
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	256820-256851	8	0.75
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP024892	Rhodococcus ruber strain YYL plasmid pYYL1.1, complete sequence	178937-178968	8	0.75
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NC_047955	Pseudomonas phage Nerthus, complete genome	9834-9865	8	0.75
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP012941	Ralstonia solanacearum strain UW163 plasmid pUW163a, complete sequence	10593-10621	8	0.724
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP012942	Ralstonia solanacearum strain UW163 plasmid pUW163b, complete sequence	27147-27175	8	0.724
NZ_CP011130_4	4.3|513788|29|NZ_CP011130|CRT	513788-513816	29	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1227837-1227865	8	0.724
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP039965	Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence	556694-556722	8	0.724
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	289539-289567	8	0.724
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	23257-23285	8	0.724
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	490979-491007	8	0.724
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	103057-103085	8	0.724
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NZ_CP016500	Agrobacterium sp. RAC06 plasmid pBSY240_1, complete sequence	242399-242427	8	0.724
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP017942	Phyllobacterium zundukense strain Tri-48 plasmid unnamed3, complete sequence	337694-337722	8	0.724
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP041164	Leisingera aquaemixtae strain R2C4 plasmid unnamed3, complete sequence	75807-75838	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_LT984809	Cupriavidus taiwanensis isolate Cupriavidus taiwanensis STM 8555 plasmid I, complete sequence	157684-157715	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_005284	Burkholderia phage phi1026b, complete genome	21671-21702	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	AF447491	Bacteriophage phiE125, complete genome	22410-22441	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	AY453853	Bacteriophage phi1026b, complete genome	21671-21702	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_003309	Burkholderia phage phiE125, complete genome	22410-22441	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP040820	Paraoceanicella profunda strain D4M1 plasmid pD4M1B, complete sequence	134383-134414	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP050093	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b5, complete sequence	449089-449120	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP020949	Rhizobium sp. CIAT894 plasmid pRheCIAT894b, complete sequence	147322-147353	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP054023	Rhizobium sp. JKLM12A2 plasmid pPR12A202, complete sequence	189265-189296	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP022566	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK02, complete sequence	363428-363459	9	0.719
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_LR594673	Variovorax sp. PBL-E5 plasmid 3	327104-327135	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP021805	Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence	152998-153029	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	78859-78890	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	85821-85852	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	92253-92284	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP054658	Lactobacillus reuteri strain AN417 plasmid pAN417A, complete sequence	52065-52096	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	21369-21400	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP024940	Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence	692657-692688	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP015734	Arthrobacter sp. U41 plasmid unnamed2, complete sequence	91531-91562	9	0.719
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP042332	Bosea sp. F3-2 plasmid pB32-1, complete sequence	64116-64147	9	0.719
NZ_CP011130_4	4.4|513842|29|NZ_CP011130|CRT	513842-513870	29	NZ_CP022666	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence	36553-36581	9	0.69
NZ_CP011130_4	4.5|513896|29|NZ_CP011130|CRT	513896-513924	29	NC_016586	Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence	269816-269844	9	0.69
NZ_CP011130_10	10.1|3461810|33|NZ_CP011130|CRISPRCasFinder	3461810-3461842	33	NZ_CP024895	Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence	190969-191001	9	0.727
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP022365	Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence	96772-96800	9	0.69
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP033323	Azospirillum brasilense strain Cd plasmid p5, complete sequence	212105-212133	9	0.69
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP032350	Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence	170331-170359	9	0.69
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP012919	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p5, complete sequence	136251-136279	9	0.69
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP032344	Azospirillum brasilense strain MTCC4038 plasmid p5, complete sequence	47194-47222	9	0.69
NZ_CP011130_20	20.2|6263326|29|NZ_CP011130|CRISPRCasFinder	6263326-6263354	29	NZ_CP033317	Azospirillum brasilense strain Sp 7 plasmid p5, complete sequence	119455-119483	9	0.69
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	1845739-1845770	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP050099	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b5, complete sequence	387077-387108	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP017943	Phyllobacterium zundukense strain Tri-48 plasmid unnamed2, complete sequence	34412-34443	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP053441	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eE, complete sequence	413289-413320	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	130515-130546	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP017148	Bosea vaviloviae strain Vaf18 plasmid unnamed1, complete sequence	211666-211697	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP053712	Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed5, complete sequence	148165-148196	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP035514	Haematobacter massiliensis strain OT1 plasmid pOT1-4, complete sequence	155620-155651	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP021083	Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence	94433-94464	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NC_023722	Rhodococcus phage ReqiPine5, complete genome	40226-40257	10	0.688
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	83041-83072	10	0.688
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	81636-81667	10	0.688
NZ_CP011130_4	4.2|513731|32|NZ_CP011130|CRT	513731-513762	32	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	773557-773588	10	0.688
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_LR594669	Variovorax sp. SRS16 plasmid 4	345748-345779	11	0.656
NZ_CP011130_4	4.1|513674|32|NZ_CP011130|CRT	513674-513705	32	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	161892-161923	17	0.469

1. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctgcgcgggaatgacgg	Protospacer
*************************.

2. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016108 (Methylomicrobium alcaliphilum 20Z plasmid MEALZ_p, complete sequence) position: , mismatch: 1, identity: 0.962

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctgcgcggggatgacga	Protospacer
******************.*******

3. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP019045 (Halioglobus pacificus strain RR3-57 plasmid pRR3-57, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

4. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

5. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

6. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

7. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

8. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

9. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

10. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

11. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

12. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016453 (Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

13. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP054615 (Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

14. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

15. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

16. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

17. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

18. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

19. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggaatgacgg	Protospacer
*********** *************.

20. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacga	Protospacer
*********.* **************

21. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgcctgcgcgggaatgacaa	Protospacer
*.**********************.*

22. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctgcgcggggatgacta	Protospacer
******************.***** *

23. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 2, identity: 0.923

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgacga	Protospacer
*.********* **************

24. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP013054 (Sinorhizobium americanum CCGM7 plasmid C, complete sequence) position: , mismatch: 3, identity: 0.897

-gtccaggtcgccctggcgctggctggctt	CRISPR spacer
tgggcagg-cgccctggcgctggctggctt	Protospacer
 *  **** *********************

25. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctttgcgggaatgacgg	Protospacer
*********** .************.

26. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccctcgcgggaatgacgg	Protospacer
**********. *************.

27. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gagtcccgccttcgcgggaatgacgg	Protospacer
** ******** *************.

28. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcggggatgacgg	Protospacer
*********** ******.******.

29. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcggaaatgacgg	Protospacer
*********** *****.*******.

30. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgacgg	Protospacer
*.********* *************.

31. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgacgg	Protospacer
*.********* *************.

32. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgacgg	Protospacer
*.********* *************.

33. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cattcccgccttcgcggggatgacga	Protospacer
 ********** ******.*******

34. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggtccccgcctgcgcgggcatgacga	Protospacer
*.*.************** *******

35. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgctttcgcgggaatgacga	Protospacer
*.*******.* **************

36. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgacaa	Protospacer
*.********* ************.*

37. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP038636 (Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctgcgcgggaatgtcat	Protospacer
********************** *. 

38. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgctttcgcgggaatgacgg	Protospacer
*********.* *************.

39. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gagtcccgccttcgcgggaatgacgg	Protospacer
** ******** *************.

40. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgcctgcgcggggatgacgg	Protospacer
***.**************.******.

41. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gtttcccgccttcgcgggaatgacgc	Protospacer
* ********* ************* 

42. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134418 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctacgcgagaatgacaa	Protospacer
***********.****.*******.*

43. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcgggagtgacgg	Protospacer
*********** *******.*****.

44. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctccgcgggaatgaggt	Protospacer
*********** *********** * 

45. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134427 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 18) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgcctacgcgggaatgacaa	Protospacer
***.*******.************.*

46. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 3, identity: 0.885

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gatccccgccttcgcgggaatgacaa	Protospacer
***.******* ************.*

47. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to NZ_CP042825 (Rhizobium sp. WL3 plasmid unnamed2, complete sequence) position: , mismatch: 4, identity: 0.84

agtcttcagcgtcatctctccagat	CRISPR spacer
cttcttcaaggtcatctctccagat	Protospacer
  ******. ***************

48. spacer 2.1|162053|25|NZ_CP011130|CRISPRCasFinder matches to MN497415 (Vibrio phage vB_VhaM_VH-8, complete genome) position: , mismatch: 4, identity: 0.84

agacttcagcgccattccaccagaa	CRISPR spacer
gtacttcaccaccattccaccagaa	Protospacer
. ****** *.**************

49. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.862

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
gtcggtcttgccgacgcgggcgccgtcgg	Protospacer
 ****.*****************.**** 

50. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gttccccgcctgcgcggggatgacgg	Protospacer
* *.**************.******.

51. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016453 (Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgctttcgcgggaatgacgc	Protospacer
*.*******.* ************* 

52. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
ggttcccgccttcgcgggaatgactg	Protospacer
*.********* ************ .

53. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134418 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cattcccgcttgcgcgggaatgacag	Protospacer
 ********.**************..

54. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134418 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattgccgcctacgcgggaatgacat	Protospacer
**** ******.************. 

55. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134417 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 8) position: , mismatch: 4, identity: 0.846

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgcctttgcgggaatgacag	Protospacer
*********** .***********..

56. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP010024 (Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
tggcgccgcacttgccgtcgccgccg	Protospacer
.*************** *******  

57. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP015737 (Shinella sp. HZN7 plasmid pShin-01, complete sequence) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
gggcgccgcgcttgccctcgccgccg	Protospacer
 ********.**************  

58. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
cggcgccgcacttgcccgcgcctcca	Protospacer
***************** **** *  

59. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
cggcgccgcacttgcccgcgcctcca	Protospacer
***************** **** *  

60. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to MF140427 (Arthrobacter phage Shrooms, complete genome) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
tggcgccgtacttgcccttgccgctc	Protospacer
.*******.*********.***** *

61. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 4, identity: 0.846

cggcgccgcacttgccctcgccgcac	CRISPR spacer
cggcgccgcccttgcgctcgccgtcc	Protospacer
********* ***** *******. *

62. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to NZ_CP006990 (Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence) position: , mismatch: 5, identity: 0.8

agtcttcagcgtcatctctccagat	CRISPR spacer
cgtcttcagcgtcacctctccatcg	Protospacer
 *************.*******   

63. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021127 (Rhizobium sp. Kim5 plasmid pRetKim5c, complete sequence) position: , mismatch: 5, identity: 0.8

agtcttcagcgtcatctctccagat	CRISPR spacer
cgtcttcagcgtcacctctccatcg	Protospacer
 *************.*******   

64. spacer 1.1|116088|25|NZ_CP011130|CRISPRCasFinder matches to CP007644 (Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence) position: , mismatch: 5, identity: 0.8

agtcttcagcgtcatctctccagat	CRISPR spacer
cgtcttcagcgtcacctctccatcg	Protospacer
 *************.*******   

65. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP023549 (Rhodobacter sp. CZR27 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.844

--ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gatgcca--tcgccgcgcgcggtgccgccgcaat	Protospacer
  * ***  *********.************.**

66. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_001381 (Mycobacterium fortuitum plasmid pAL5000, complete sequence) position: , mismatch: 5, identity: 0.844

ttcgatgcc-gccgttcgcggtcaggttggtgc	CRISPR spacer
-tggctgccagccgttcgcgggctggttggtgc	Protospacer
 * * **** *********** * *********

67. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP039909 (Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence) position: , mismatch: 5, identity: 0.828

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
atcatggccgccgatccggctgctgttgc	Protospacer
 **  ********.**.************

68. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP011248 (Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence) position: , mismatch: 5, identity: 0.828

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
ctcccggccgccgttctggctgctgatcc	Protospacer
.*** ******** *********** * *

69. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP032919 (Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence) position: , mismatch: 5, identity: 0.828

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
ctcccggccgccgttctggctgctgatcc	Protospacer
.*** ******** *********** * *

70. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP033029 (Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence) position: , mismatch: 5, identity: 0.828

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
ctcccggccgccgttctggctgctgatcc	Protospacer
.*** ******** *********** * *

71. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022991 (Paraburkholderia aromaticivorans strain BN5 plasmid pBN1, complete sequence) position: , mismatch: 5, identity: 0.828

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgaggcgggggcaatggc	Protospacer
************** ***** ** .* **

72. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NC_009427 (Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence) position: , mismatch: 5, identity: 0.828

ctcggccttgccgacgcgggcgctgtcgc-	CRISPR spacer
cccggcctcgccgacgcgggcgc-gcggca	Protospacer
*.******.************** *. ** 

73. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 5, identity: 0.828

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctgaaggtcggcctggcgctggcgggctt	Protospacer
 *  ****** ************ *****

74. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 5, identity: 0.828

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctgaaggtcggcctggcgctggcgggctt	Protospacer
 *  ****** ************ *****

75. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP013635 (Rhizobium sp. N324 plasmid pRspN324e, complete sequence) position: , mismatch: 5, identity: 0.828

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ggccagctcgccctggcgcttgctgagtt	Protospacer
* **** ************* ****. **

76. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP030763 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed3, complete sequence) position: , mismatch: 5, identity: 0.815

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
cttcctggctgcggcgacgcagcgaac	Protospacer
*.  ** *******************.

77. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP012886 (Mycobacterium chimaera strain AH16 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
gcggctcgccgcggcgacgtagcgacc	Protospacer
 ********.*********.***** .

78. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016453 (Sphingobium sp. RAC03 plasmid pBSY17_1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
catttccgactgcgcgggaatgacct	Protospacer
 ***.*** ***************  

79. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP054615 (Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
gattcccgccttcgcggggatgatcg	Protospacer
*********** ******.****. .

80. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
agttcccgccttcgcgggaatgactg	Protospacer
..********* ************ .

81. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134417 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 8) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cattcccacctacgcgggaatgacag	Protospacer
 ******.***.************..

82. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

83. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

84. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

85. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

86. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

87. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

88. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

89. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

90. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

91. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

92. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

93. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

94. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

95. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

96. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

97. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

98. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

99. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

100. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134428 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 19) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
aattctcgcctacgcgggaatgacag	Protospacer
.****.*****.************..

101. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

102. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134420 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 11) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cattcccgcctacgcgggaatggcag	Protospacer
 **********.**********.*..

103. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

104. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 5, identity: 0.808

gattcccgcctgcgcgggaatgacga	CRISPR spacer
cttggccgcctgctcgggaatgacga	Protospacer
  *  ******** ************

105. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to CP009870 (Pantoea sp. PSNIH2 plasmid pPSP-b98, complete sequence) position: , mismatch: 5, identity: 0.808

cggcgccgcacttgccctcgccgcac	CRISPR spacer
ggccgccgcccttgccctcgccgccg	Protospacer
 * ****** **************  

106. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 5, identity: 0.808

cggcgccgcacttgccctcgccgcac	CRISPR spacer
aggcgccgctctcgccctcgccgccg	Protospacer
 ******** **.***********  

107. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 5, identity: 0.808

cggcgccgcacttgccctcgccgcac	CRISPR spacer
aggcgccgctctcgccctcgccgccg	Protospacer
 ******** **.***********  

108. spacer 20.1|6263266|26|NZ_CP011130|CRISPRCasFinder matches to NZ_CP004394 (Celeribacter indicus strain P73 plasmid pP73A, complete sequence) position: , mismatch: 5, identity: 0.808

cggcgccgcacttgccctcgccgcac	CRISPR spacer
cgacgccgcccttgccctcgccggtg	Protospacer
**.****** *************   

109. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP017304 (Rhodococcus sp. YL-1 plasmid pYLL2 sequence) position: , mismatch: 6, identity: 0.812

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
tccgcgatcgccgcgcccggtgccggcgcgat	Protospacer
*.*  *.********* ******** ******

110. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP017664 (Cronobacter sp. JZ38 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.812

--ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cctgtcag--cgcggcgcacgctgccgccgcgat	Protospacer
  * .***  *** ******* ************

111. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP048283 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248c, complete sequence) position: , mismatch: 6, identity: 0.793

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
cgcacggccggcggtcttgctgctgttgc	Protospacer
. *  ***** ****** ***********

112. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP021802 (Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence) position: , mismatch: 6, identity: 0.793

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
gtcattcccgccggtctggctgcggttgc	Protospacer
 **    **************** *****

113. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 6, identity: 0.793

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
gtccagggcgccggtctggctgttgccgt	Protospacer
 ****** **************.**..*.

114. spacer 4.3|513788|29|NZ_CP011130|CRT matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 6, identity: 0.793

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
cttcgggccgccggtcgggctggtgttgg	Protospacer
.*.*.*********** ***** ***** 

115. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP035502 (Sphingosinicella sp. BN140058 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.793

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
taccgggccgccggtctgcctgctgatct	Protospacer
* **.************* ****** * .

116. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013524 (Rhizobium phaseoli strain R744 plasmid pRphaR744b, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

117. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013559 (Rhizobium phaseoli strain N841 plasmid pRphaN841b, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

118. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013576 (Rhizobium phaseoli strain N671 plasmid pRphaN671b, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

119. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013548 (Rhizobium phaseoli strain R611 plasmid pRetR611a, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

120. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013528 (Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcccacgcgggcgctgagcc	Protospacer
  ********** ************   *

121. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013533 (Rhizobium phaseoli strain R650 plasmid pRphaR650a, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

122. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013543 (Rhizobium phaseoli strain R620 plasmid pRphaR620a, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

123. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ggtggcctcgccgacgcggccgctgtcgt	Protospacer
  .*****.********** ********.

124. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013581 (Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcccacgcgggcgctgagcc	Protospacer
  ********** ************   *

125. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP013570 (Rhizobium phaseoli strain N771 plasmid pRphaN771b, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgcctacgcgggcgctgagcc	Protospacer
  ********** ************   *

126. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP020471 (Rhodobacter blasticus strain 28/5 plasmid pRsa, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
atgatccttgccgacgggggcgatgtcgc	Protospacer
 * . *********** ***** ******

127. spacer 4.4|513842|29|NZ_CP011130|CRT matches to CP021183 (Sphingomonas wittichii DC-6 plasmid pDC02, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgacgccggcgggcgagc	Protospacer
***************** ****     **

128. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ccagccgttgccgacgcggacgctgtcgg	Protospacer
*. * * ************.******** 

129. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ccagccgttgccgacgcggacgctgtcgg	Protospacer
*. * * ************.******** 

130. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ccagccgttgccgacgcggacgctgtcgg	Protospacer
*. * * ************.******** 

131. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP044217 (Mesorhizobium sp. NIBRBAC000500504 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
gccggccttgccggcgcgggcgcgggctc	Protospacer
 .***********.********* * * *

132. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.793

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ccagccgttgccgacgcggacgctgtcgg	Protospacer
*. * * ************.******** 

133. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gagcaggtcgccctcgcgctggatggcgg	Protospacer
*  *********** ******* ****  

134. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctcatcctcgccctggccctggctggctt	Protospacer
 **    ********** ***********

135. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP049249 (Rhizobium rhizoryzae strain DSM 29514 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtccagatcgcccgggcgctggctcaatc	Protospacer
******.****** ********** . *.

136. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctcatcctcgccctggccctggctggctt	Protospacer
 **    ********** ***********

137. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
aaacaggtcgccctgccgcttgctggcct	Protospacer
.  ************ **** ******.*

138. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_LR594690 (Variovorax sp. WDL1 plasmid 2) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctcatcctcgccctggccctggctggctt	Protospacer
 **    ********** ***********

139. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_HG938356 (Neorhizobium galegae bv. officinalis bv. officinalis str. HAMBI 1141 plasmid pHAMBI1141a, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
aaacaggtcgccctgccgcttgctggcct	Protospacer
.  ************ **** ******.*

140. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctcatcctcgccctggccctggctggctt	Protospacer
 **    ********** ***********

141. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
cagccggtcggcctggcgctggcgggctt	Protospacer
   * ***** ************ *****

142. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtcgaggtcgccctggcgcaggcggattg	Protospacer
*** *************** *** *..* 

143. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP024314 (Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtccagatcaccctggcgctggcatggtc	Protospacer
******.**.*************  * *.

144. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtcatggtcgccctggcgctggcgcgcgg	Protospacer
***  ******************  **  

145. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP041605 (Streptomyces sp. S1D4-14 plasmid pS1D4-14.1, complete sequence) position: , mismatch: 6, identity: 0.793

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ggccagatcgccctggcgccggctgcccg	Protospacer
* ****.************.***** *. 

146. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022999 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
tttcctcgctgcggcgacgcagcgcac	Protospacer
..  ******************** *.

147. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

148. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

149. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

150. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

151. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcggtgcgccgacgcagcacgc	Protospacer
******** **** *********. ..

152. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

153. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

154. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

155. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP047174 (Rathayibacter sp. VKM Ac-2760 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
cctgctcgctgcggcgacgctgctggg	Protospacer
** ***************** ** .. 

156. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

157. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

158. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

159. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

160. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

161. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

162. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

163. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

164. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

165. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

166. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

167. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

168. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

169. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

170. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

171. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcggtgcgccgacgcagcacgc	Protospacer
******** **** *********. ..

172. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

173. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

174. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcggtgcgccgacgcagcacgc	Protospacer
******** **** *********. ..

175. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcggtgcgccgacgcagcacgc	Protospacer
******** **** *********. ..

176. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcggtgcgccgacgcagcacgc	Protospacer
******** **** *********. ..

177. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

178. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

179. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

180. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

181. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

182. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

183. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

184. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

185. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

186. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

187. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

188. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

189. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

190. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

191. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

192. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

193. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

194. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

195. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

196. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

197. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

198. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

199. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

200. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

201. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

202. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

203. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

204. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

205. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

206. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

207. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

208. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

209. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

210. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

211. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

212. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

213. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

214. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

215. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

216. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

217. spacer 10.2|3461867|27|NZ_CP011130|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.778

ccggctcgctgcggcgacgcagcgaat	CRISPR spacer
ccggctcgctgcggcggcgcaccagca	Protospacer
****************.**** *..  

218. spacer 16.1|5199383|26|NZ_CP011130|CRISPRCasFinder matches to NZ_LR134429 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 20) position: , mismatch: 6, identity: 0.769

gattcccgcctgcgcgggaatgacga	CRISPR spacer
agatcccgccttcgcgggaatgacac	Protospacer
.. ******** ************. 

219. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to MN855768 (Siphoviridae sp. isolate 183, complete genome) position: , mismatch: 6, identity: 0.793

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
gagcactcttggctttgtcggcatcggct	Protospacer
  ***********.*********.**  *

220. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggtcgccccgcacgatgccgccgagcc	Protospacer
..********** ******.******** * .

221. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggtcgccccgcacgatgccgccgagcc	Protospacer
..********** ******.******** * .

222. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggtcgccccgcacgatgccgccgagcc	Protospacer
..********** ******.******** * .

223. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP026308 (Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggtcgccccgcacgatgccgccgagcc	Protospacer
..********** ******.******** * .

224. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggtcgccccgcacgatgccgccgagcc	Protospacer
..********** ******.******** * .

225. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP013381 (Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence) position: , mismatch: 7, identity: 0.781

ttccagg---tcgccgcgcacggtgccgccgcgat	CRISPR spacer
---cgggatctcgacgcgcacggtgccgccgcgcc	Protospacer
   *.**   *** ******************* .

226. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP009547 (Burkholderia sp. 2002721687 plasmid pBTU, complete sequence) position: , mismatch: 7, identity: 0.781

ttccagg---tcgccgcgcacggtgccgccgcgat	CRISPR spacer
---cgggatctcgacgcgcacggtgccgccgcgcc	Protospacer
   *.**   *** ******************* .

227. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_LR134451 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccg-ccgcgat	CRISPR spacer
ccccaggtcgccgtgcacggcgccgaccttga-	Protospacer
..***********.******.**** ** .** 

228. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_012725 (Burkholderia glumae BGR1 plasmid bglu_4p, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgcc-gcgat	CRISPR spacer
gaacaggtcacggcgcacggtgccgcctgcgg-	Protospacer
   ******.* *************** ***. 

229. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gccgacgtcgccgcgcacggtgcggcggcgct	Protospacer
 .* * ***************** ** *** *

230. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP035902 (Burkholderia glumae strain 257sh-1 plasmid plas1, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgcc-gcgat	CRISPR spacer
gaacaggtcacggcgcacggtgccgcctgcgg-	Protospacer
   ******.* *************** ***. 

231. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP052865 (Burkholderia glumae strain HN1 plasmid pBGHN1-1, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgcc-gcgat	CRISPR spacer
gaacaggtcacggcgcacggtgccgcctgcgg-	Protospacer
   ******.* *************** ***. 

232. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.781

ttccaggtcgccgcgcacggtgccgccgcgat-	CRISPR spacer
cttgaggtcgacgcgcacggtgtcgcc-cgttc	Protospacer
.*. ****** ***********.**** ** * 

233. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MF324914 (Mycobacterium phage Krueger, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
cgccacaccgtcgttcgcggtcaggttggtga	Protospacer
. * *..***.******************** 

234. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN234223 (Mycobacterium phage Philly, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gttgacgccgccgttcgcgatcaggtcgatac	Protospacer
 *.**.*************.******.*.*.*

235. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KP027207 (Mycobacterium phage Chandler, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

236. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN096360 (Mycobacterium phage Rita1961, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

237. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MG839014 (Mycobacterium phage RagingRooster, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

238. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KJ194581 (Mycobacterium phage Audrey, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

239. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KR080203 (Mycobacterium phage OrangeOswald, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

240. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MH513976 (Mycobacterium phage Morty007, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

241. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MH051265 (Mycobacterium phage Yahalom, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

242. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MH316565 (Mycobacterium phage Mortcellus, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

243. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MT310871 (Mycobacterium phage Jackstina, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

244. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MK359357 (Mycobacterium phage RomaT, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

245. spacer 4.2|513731|32|NZ_CP011130|CRT matches to JF704095 (Mycobacterium phage Daisy, complete sequence) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

246. spacer 4.2|513731|32|NZ_CP011130|CRT matches to EU816589 (Mycobacterium phage Phaedrus, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

247. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN096359 (Mycobacterium phage Obutu, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

248. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MK061414 (Mycobacterium phage Marley1013, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

249. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MT952851 (Mycobacterium phage Gervas, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

250. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MG925353 (Mycobacterium phage Nozo, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

251. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KJ194584 (Mycobacterium phage Heathcliff, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

252. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN444872 (Mycobacterium phage SynergyX, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

253. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KY945355 (Mycobacterium phage Shandong1, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gtcgataacgccgttcgcggtcagcgtcgcgc	Protospacer
 *****. ****************  * *.**

254. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MH576977 (Mycobacterium phage Tydolla, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

255. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MG925338 (Mycobacterium phage ChaChing, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

256. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_023742 (Mycobacterium phage Akoma, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

257. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MG920059 (Mycobacterium phage Baloo, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

258. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_023686 (Mycobacterium phage Gadjet, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

259. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KR080205 (Mycobacterium phage Corofin, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

260. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_041965 (Mycobacterium phage Athena, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

261. spacer 4.2|513731|32|NZ_CP011130|CRT matches to DQ398049 (Mycobacterium phage Pipefish, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

262. spacer 4.2|513731|32|NZ_CP011130|CRT matches to KF493879 (Mycobacterium phage Bernardo, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

263. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MT310892 (Mycobacterium phage Compostia, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

264. spacer 4.2|513731|32|NZ_CP011130|CRT matches to JN699018 (Mycobacterium phage Kamiyu, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

265. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_012027 (Mycobacterium phage Phlyer, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

266. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN444873 (Mycobacterium phage Abinghost, complete genome) position: , mismatch: 7, identity: 0.781

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
attgacgccgccgttcgcgatcaggtcgatcc	Protospacer
 *.**.*************.******.*.* *

267. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.759

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
gttgccgccgacggtctgggtgctgttgc	Protospacer
 *.   **** ******** *********

268. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NC_007950 (Polaromonas sp. JS666 plasmid 2, complete sequence) position: , mismatch: 7, identity: 0.759

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
cgcctggccgccggtctggccgctgcggg	Protospacer
. ** ***************.****. * 

269. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgaagcgggcgacgcgct	Protospacer
************** ******* .*.  .

270. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032328 (Azospirillum brasilense strain MTCC4035 plasmid p7, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
gccggccttggcgacgcgggcggtgtgct	Protospacer
 .******** *********** ***  .

271. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032328 (Azospirillum brasilense strain MTCC4035 plasmid p7, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
gccggccttggcgacgcgggcggtgtgct	Protospacer
 .******** *********** ***  .

272. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgaagcgggcgacgcgct	Protospacer
************** ******* .*.  .

273. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032685 (Rhizobium sp. CCGE531 plasmid pRCCGE531d, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgatgcggccgcggatct	Protospacer
**************.**** *** * . .

274. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP032690 (Rhizobium sp. CCGE532 plasmid pRCCGE532d, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgatgcggccgcggatct	Protospacer
**************.**** *** * . .

275. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP017750 (Cupriavidus sp. USMAA2-4 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
agcggccttgccgacgccggcgccctgcc	Protospacer
  *************** *****. *  *

276. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022999 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgatgcggccgcggatct	Protospacer
**************.**** *** * . .

277. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ggtgacctggccgacgcgggcgttgtcga	Protospacer
  .*.*** *************.***** 

278. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
tacagccttgcccacgcgggcgcggtcca	Protospacer
. *.******** ********** ***  

279. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NC_010492 (Arthrobacter sp. Chr15 plasmid pChr15, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcgaccttgccggcgcgggcgcccggga	Protospacer
****.********.*********.   * 

280. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP048426 (Rhizobium daejeonense strain KACC 13094 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
ctcggccttgccgatgcggccgcggattt	Protospacer
**************.**** *** * . .

281. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
tacagccttgcccacgcgggcgcggtcca	Protospacer
. *.******** ********** ***  

282. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
tacagccttgcccacgcgggcgcggtcca	Protospacer
. *.******** ********** ***  

283. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 7, identity: 0.759

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
cgcgcccttgccgacgctggcgctggtca	Protospacer
* ** ************ ******* .  

284. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.759

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtcgagctcgccctggcgctggcgcatgt	Protospacer
*** ** ****************  .. *

285. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 7, identity: 0.759

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
atgggcgtcgccctgccgctggctgactt	Protospacer
.*  . ********* *********.***

286. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 7, identity: 0.759

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
gtccaggtcgccctgggtctggcgcacca	Protospacer
****************  *****  .*. 

287. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP003988 (Streptomyces sp. 769 plasmid pSGZL, complete sequence) position: , mismatch: 7, identity: 0.759

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctccacgtcgccctggcgctgggtcagtg	Protospacer
 **** **************** * . * 

288. spacer 4.5|513896|29|NZ_CP011130|CRT matches to MN657148 (Polaromonas sp. strain ANT_J29B plasmid pA29BJ2, complete sequence) position: , mismatch: 7, identity: 0.759

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ggtcaggtcgcgcaggcgctggctggtga	Protospacer
* .******** * ************.  

289. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022775 (Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

290. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

291. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

292. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP023017 (Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

293. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

294. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

295. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

296. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

297. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

298. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

299. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022764 (Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

300. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022797 (Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

301. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022758 (Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.788

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
cgcggtcggccgcgggatcgccgagctgatccg	Protospacer
 ** ************ ********* . * **

302. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP007214 (Burkholderia plantarii strain ATCC 43733 plasmid bpln_1p, complete sequence) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gaacaggtcgcggcgcacggtgccgccggccg	Protospacer
   ******** ****************    

303. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
atccaggtcgccgcgcagggcgccgcccttcg	Protospacer
 **************** **.****** .   

304. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP031358 (Erythrobacter aureus strain YH-07 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gagaaggtcgccgcgcacggtcacgccgtgtt	Protospacer
    *****************  *****.* *

305. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gacgcggtcggcgcgcagggtgccgccggcat	Protospacer
  *  ***** ****** **********  **

306. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_013193 (Candidatus Accumulibacter phosphatis clade IIA str. UW-1 plasmid pAph01, complete sequence) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ttcggccacgccgcccacggtgccgccccgac	Protospacer
*** .   ****** ************ ***.

307. spacer 4.1|513674|32|NZ_CP011130|CRT matches to MH727545 (Mycobacterium phage DismalStressor, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

308. spacer 4.1|513674|32|NZ_CP011130|CRT matches to KJ510412 (Mycobacterium phage ZoeJ, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcggtgct	Protospacer
. .****.************** *** *.* *

309. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_026598 (Mycobacterium phage Milly, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

310. spacer 4.1|513674|32|NZ_CP011130|CRT matches to MH834601 (Mycobacterium phage BoostSeason, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

311. spacer 4.1|513674|32|NZ_CP011130|CRT matches to KX688047 (Mycobacterium phage Marcoliusprime, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

312. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_028759 (Mycobacterium phage Mufasa, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

313. spacer 4.1|513674|32|NZ_CP011130|CRT matches to MF140408 (Mycobacterium phage DismalFunk, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

314. spacer 4.1|513674|32|NZ_CP011130|CRT matches to MF140411 (Mycobacterium phage Findley, complete genome) position: , mismatch: 8, identity: 0.75

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtcaggccgccgcgcacggtgacgcgccgct	Protospacer
. .****.************** ***  ** *

315. spacer 4.2|513731|32|NZ_CP011130|CRT matches to MN945901 (Mycobacterium phage Ximenita, complete genome) position: , mismatch: 8, identity: 0.75

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
cgccacaccgccgttcgcggtcacgttcgtga	Protospacer
. * *..**************** *** *** 

316. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP017563 (Paraburkholderia sprentiae WSM5005 plasmid pl1WSM5005, complete sequence) position: , mismatch: 8, identity: 0.75

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
ttcgatgccggccttcgcggtcatatagatcg	Protospacer
********** * ********** .* *.*  

317. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.75

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
caggatgccgccgttggcggtctggtccgggc	Protospacer
.  ************ ****** ***. * **

318. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP024892 (Rhodococcus ruber strain YYL plasmid pYYL1.1, complete sequence) position: , mismatch: 8, identity: 0.75

ttcgatgccgccgttcgcggtcaggttggtgc--	CRISPR spacer
cccgaggccggcgttcgcggtcaggc--gtactg	Protospacer
..*** **** **************.  **.*  

319. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NC_047955 (Pseudomonas phage Nerthus, complete genome) position: , mismatch: 8, identity: 0.75

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
cacgaccgcgccgttctcggtcagcttggtgg	Protospacer
. ***.  ******** ******* ****** 

320. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP012941 (Ralstonia solanacearum strain UW163 plasmid pUW163a, complete sequence) position: , mismatch: 8, identity: 0.724

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
aaatcggccgccggtcaggatgctgttga	Protospacer
   . *********** ** ******** 

321. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP012942 (Ralstonia solanacearum strain UW163 plasmid pUW163b, complete sequence) position: , mismatch: 8, identity: 0.724

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
aaatcggccgccggtcaggatgctgttga	Protospacer
   . *********** ** ******** 

322. spacer 4.3|513788|29|NZ_CP011130|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 8, identity: 0.724

ttccaggccgccggtctggctgctgttgc	CRISPR spacer
cgccatgccgctggtctggctgctgggcg	Protospacer
. *** *****.*************    

323. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP039965 (Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.724

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
atcggccttggcgacgcgggcggcttgct	Protospacer
 ********* *********** . *  .

324. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.724

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
cagcaggtcgccctggcgcaggctgtggc	Protospacer
   **************** *****   .

325. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 8, identity: 0.724

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
atgggctgcgccctggcgctggccggctt	Protospacer
.*  .   ***************.*****

326. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.724

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
atgggctgcgccctggcgctggcgggctt	Protospacer
.*  .   *************** *****

327. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 8, identity: 0.724

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
atggcttgcgccctggcgctggccggctt	Protospacer
.*      ***************.*****

328. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NZ_CP016500 (Agrobacterium sp. RAC06 plasmid pBSY240_1, complete sequence) position: , mismatch: 8, identity: 0.724

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
ctccaggttgccctgacgctggctctaga	Protospacer
 *******.******.********     

329. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP017942 (Phyllobacterium zundukense strain Tri-48 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.724

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
gactgatcttgcccttgtcggcaccgcaa	Protospacer
   .. ***** **************** 

330. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP041164 (Leisingera aquaemixtae strain R2C4 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gaagcggtcgccgggcaccgtgccgccgcgca	Protospacer
     ******** **** ***********  

331. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_LT984809 (Cupriavidus taiwanensis isolate Cupriavidus taiwanensis STM 8555 plasmid I, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ccccaggacgccgcgcacggtgccggaacagg	Protospacer
..***** *****************  .*.. 

332. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_005284 (Burkholderia phage phi1026b, complete genome) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtgcgatcgccgcgcacgatgccgccgcgtc	Protospacer
. .  *.************.********** .

333. spacer 4.1|513674|32|NZ_CP011130|CRT matches to AF447491 (Bacteriophage phiE125, complete genome) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtgcgatcgccgcgcacgatgccgccgcgtc	Protospacer
. .  *.************.********** .

334. spacer 4.1|513674|32|NZ_CP011130|CRT matches to AY453853 (Bacteriophage phi1026b, complete genome) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtgcgatcgccgcgcacgatgccgccgcgtc	Protospacer
. .  *.************.********** .

335. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_003309 (Burkholderia phage phiE125, complete genome) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
cgtgcgatcgccgcgcacgatgccgccgcgtc	Protospacer
. .  *.************.********** .

336. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP040820 (Paraoceanicella profunda strain D4M1 plasmid pD4M1B, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
ctcgaggtcgccgcgcgcggtgccggtgtcgg	Protospacer
.** ************.******** .*. . 

337. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP050093 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b5, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
aaccgcatcgtggcgcacggtgccgccgcgcg	Protospacer
  **. .***. ******************  

338. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP020949 (Rhizobium sp. CIAT894 plasmid pRheCIAT894b, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
tgacagttcgccgcgcacggtgcagcacaaac	Protospacer
*  *** **************** **   .*.

339. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP054023 (Rhizobium sp. JKLM12A2 plasmid pPR12A202, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gaccgcatcgtggcgcacggtgccgccgcgcg	Protospacer
  **. .***. ******************  

340. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP022566 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK02, complete sequence) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gaccgcatcgtggcgcacggtgccgccgcgcg	Protospacer
  **. .***. ******************  

341. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_LR594673 (Variovorax sp. PBL-E5 plasmid 3) position: , mismatch: 9, identity: 0.719

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gccgcgatcgccgcgcacgatgccggcgcgca	Protospacer
 .*  *.************.***** ****  

342. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP021805 (Sinorhizobium meliloti strain T073 plasmid psymA, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
cgtcttgccgccgtgcgcggtcgggttggtca	Protospacer
. .  ********* *******.*******  

343. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gatgctgccgccgttggcggtcaggctggccg	Protospacer
  .* ********** *********.***.  

344. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gatgctgccgccgttggcggtcaggctggccg	Protospacer
  .* ********** *********.***.  

345. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gatgctgccgccgttggcggtcaggctggccg	Protospacer
  .* ********** *********.***.  

346. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP054658 (Lactobacillus reuteri strain AN417 plasmid pAN417A, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
atcgatgccgccgtcagcggtcagctgaaagg	Protospacer
 *************. ******** * .. * 

347. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
atgctggccgccgttcacggccaggttggcac	Protospacer
 *    **********.***.********..*

348. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP024940 (Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
cgtgtagatgccgttcgcggtcaagttgctgc	Protospacer
. .*  * .**************.**** ***

349. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP015734 (Arthrobacter sp. U41 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
ggcgatgcggccgttcgcgatcagggccgagg	Protospacer
  ****** **********.***** . * * 

350. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP042332 (Bosea sp. F3-2 plasmid pB32-1, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
catgaaaaggccgttcgcggtcaggaaggtgc	Protospacer
. .** .  ****************  *****

351. spacer 4.4|513842|29|NZ_CP011130|CRT matches to NZ_CP022666 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence) position: , mismatch: 9, identity: 0.69

ctcggccttgccgacgcgggcgctgtcgc	CRISPR spacer
tcttctctttccgacgcgggcgctgtctt	Protospacer
...  .*** ***************** .

352. spacer 4.5|513896|29|NZ_CP011130|CRT matches to NC_016586 (Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence) position: , mismatch: 9, identity: 0.69

gtccaggtcgccctggcgctggctggctt	CRISPR spacer
cagcaggtcgccctggcgcaggctatggc	Protospacer
   **************** ****.   .

353. spacer 10.1|3461810|33|NZ_CP011130|CRISPRCasFinder matches to NZ_CP024895 (Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

ggctgtcggccgcgggttcgccgagcaattgcg	CRISPR spacer
ccctgtcggccgggggttcgccgggcgcgtcct	Protospacer
  ********** **********.**.  * * 

354. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP022365 (Azospirillum sp. TSH58 plasmid TSH58_p06, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

355. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP033323 (Azospirillum brasilense strain Cd plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

356. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP032350 (Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

357. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP012919 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p5, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

358. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP032344 (Azospirillum brasilense strain MTCC4038 plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

359. spacer 20.2|6263326|29|NZ_CP011130|CRISPRCasFinder matches to NZ_CP033317 (Azospirillum brasilense strain Sp 7 plasmid p5, complete sequence) position: , mismatch: 9, identity: 0.69

tcgcactcttggccttgtcggcaccgcat	CRISPR spacer
agctgctcttggccttgtcggccccgatg	Protospacer
   ..***************** ***   

360. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
acgtaggtccacgcgcacggtgccgccgaaca	Protospacer
 . .*****  ***************** .  

361. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP050099 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b5, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
aacggcatcgtggcgcacggtgccgccgcgcg	Protospacer
  * . .***. ******************  

362. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP017943 (Phyllobacterium zundukense strain Tri-48 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gatcaggtcgccgcgcaccgtgcagcagatgc	Protospacer
  .*************** **** ** *  ..

363. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP053441 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eE, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
aacggcatcgtggcgcacggtgccgccgcgcg	Protospacer
  * . .***. ******************  

364. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
tcaaccgtcgccgcggtcggtgccgccgccgc	Protospacer
*.    *********  ************ ..

365. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP017148 (Bosea vaviloviae strain Vaf18 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gatcaggtcgccgcgaacggtgcagcagatgc	Protospacer
  .************ ******* ** *  ..

366. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP053712 (Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed5, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gatcaggtcgccacgcacggtgcagcagatgc	Protospacer
  .*********.********** ** *  ..

367. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP035514 (Haematobacter massiliensis strain OT1 plasmid pOT1-4, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gcgcgcgtcgccgcgccctgtgccgccgcccg	Protospacer
 . *. ********** * **********   

368. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP021083 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gagcaggtcgccgcgcagggtgcagcagatgc	Protospacer
   ************** ***** ** *  ..

369. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NC_023722 (Rhodococcus phage ReqiPine5, complete genome) position: , mismatch: 10, identity: 0.688

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gagaagatcaccgcgcacggtgccgcccgcgt	Protospacer
    **.**.*****************   .*

370. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 10, identity: 0.688

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gccgttgccgccggtcgcggtcagggagaccg	Protospacer
 .** ******** ***********  *..  

371. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 10, identity: 0.688

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gccgttgccgccggtcgcggtcagggagaccg	Protospacer
 .** ******** ***********  *..  

372. spacer 4.2|513731|32|NZ_CP011130|CRT matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 10, identity: 0.688

ttcgatgccgccgttcgcggtcaggttggtgc	CRISPR spacer
gatgatgccgccgttggcggccaggtccttca	Protospacer
  .************ ****.*****.  *  

373. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_LR594669 (Variovorax sp. SRS16 plasmid 4) position: , mismatch: 11, identity: 0.656

ttccaggtcgccgcgcacggtgccgccgcgat	CRISPR spacer
gcggccatcgccgcgcacgatgccggcgcgca	Protospacer
 .    .************.***** ****  

374. spacer 4.1|513674|32|NZ_CP011130|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 17, identity: 0.469

ttccaggtcgccgcgcacggtgccgccgcgat---	CRISPR spacer
---agggcggcggcacggtgcgccgcgacggcgat	Protospacer
    .**. ** **.*.  *.***** .**..   

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	5862467 : 5871198	12	Acidithiobacillus_phage(87.5%)	NA	NA
DBSCAN-SWA_2	5880788 : 5924616	38	Pseudomonas_phage(35.0%)	capsid,portal,head,transposase,terminase	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP011130|5862467:5871198|DBSCAN-SWA
CTCATGCCCCCTGCTCCTTCTTGTCGTGATTAGATCGCAAGCCAAAGAACGCTGGCCCCGACCACCGGGTCCCGGTGATCTCCCTCGCCACCTTCGACAAGCTGCCGAACGTCCTGCCCTGATACTCAAAGACATCGCCGTCGAGCACCTTCACCCGGTGAACTTGGCCGTTATGGACGCGGGTAAGCACGCTGCCCACCAACGGAGCAACCTGCGTTTTCCGTCGGGAGACGCGCCCCGTATCGAGCAATTGTTTAACGCGCCGTTCGTTCTCTGAAATCAGCGACGGCTGGGATATCCGATACGCATCTTCTTGAATGCGATGAGCTAGTCGCCGCACCACGTACCGCCGGTTGTTGATACCCGGAGGTTCACCGAACAACGCGATCCAACGTGCTTTTAGTTGACTCCAAGGCATATCCGGCAATGCAGCAACCTGCGCTGCGGTAGACGCCGCTTCTTCCGACGATGACGATGACACGCTAGCCTCCAGGGCTCTCCAAGGAGTTGACATGGACACTCGGGTGGCCTGGTTTATCAAGTCCAACTTCGCCGGATGGCGACGACGTTCTGACCGCGCTCTTTCGCAATCGCACAAGCGCATACGCGATGATCTGTGCTACAGCCTGATTGCGATCAGCTGTCGATCGGATGGCGGCTTTTAACGGTTTCTCGCTCACTTCTCGCACTCCTTCTGCGGGATGGGCTTACCCGATTTGGATCGGCGACGTTCTTGGGGAGCACTTCGTCTCGGACCGCGACCTCGCCGTTGTTCCATTCGATGAAGCGAGCGAAGTCGTCACGGGCGCAGATCTGGCGCGGGCTCGTGACTTGTCCTTTGTATTTGGCGCGCCGCAGCACCCACTCCAATTTCGGACGCCGGTGGCCTGATGCGTGCGCCTCAGCCAACGCGAGGATGAAGTCGCGCTGCTTGCGATACAGAAATAGGTCCTGACCGTTCATTCGCAGACGCGAGCCATCCGCGCTGACGTCGAACCACAGGTTGTCGTCGCGCGGGCGCATCTGCACCGAAATCGCAGGCACCACCAAGCCACCTAGCCGATCAAGGTCGAGCAACAGCCCCTGCGGCTCCAATTTGGCGACCTGGATCAACGGCACTACCATGCGACTGGAATCGCTGATGTCGCGCGTGAGCACCTTGGACGTGGTCAGCACCATCTGGCTTGCAGCCTCCTCGTCCACCAGCGCCCGCACCACAGGCTCGTATTCCACGTGCCAACCGCATCGGAGCAAGTAGATCGAGACGCTGCCACTCGCGGTCGGCAACATCGCCAGTCGCCACAAGCGGTACGGCAACAGCTCGATTGCTCTGGCGCCGTCGCCTGCCATGGCCTCGCTCAATACCTTCGGTAACCACTCGTGGCGGACCTGAGCGGCCTGGAACGCCGGCCACGTGTCCACTTCCCCGCCGCAGACACCGCAGCGCAGCGCATGATCGCTGTAGCTATAGACCTGGCGTGTGTCGACAAAGCGGCACGCTTTGCAGGTCCAGCGCACAGCGCGTTTGGCCGGATGCATCGCACCCAGATCGATCAATGCACTTTGTAGGCCACCGCCGCTTGAAGGCAGCAGAGCCCCGACCGGTTCGGTTTCGAACCGGTGAAGGTAATTTCTGAGCAAGGCAAAGCTTCCTTACCGAAGGAATACGCGGACGTAACTGCCCGTCAAATCGTTTCCGATCTGAAGTTGATTCATATGCGTTTCGCAGGGGCGTACGTGCCCGTCAGGTCGCTACCGACCTCAAAGCGAATACAAGCGTTACAAGTGCCTCAGCGAATCGGCGAGGCCGATTGCAGATGCATACCTTGTTGTTTGCAAATCACGCGTTCGAAAACGTGGCCGCAATCGCGATCCGGAATGCCGGACGCTGTCCCTGGTAGGAAGTAGTTTGTATACGGGGCTGACAAGGTTGCCGTCAGCGTGTGGCGAAGTACCAATCCATTGTTCATTGTCAGGTCTCCTTGCTGAGACCGCTTTTAGTTGTTGTTGTGTTGCCTGAACAAAGACTATCGCGCAGATGGGCGGCCACGCAATATCACAAGCGCGCCCAAATGCAAATCACACGGGACTGTCTGAACGCTGATTCATTCTAGGTTAGAAAAACAGCCAATTTTTCGATGTTTTCTGTATGTGTTGCTATCGATTGCTAGCCATTCGTAGTTGGTTCGTAGCTGGTTTCTTCTTCCGTTCGTAGCCGACTTGGGTAGACGCTCTTTGTGCCGGTGCATTCGCGCCGACAGCACCAAGAGGAGTTCTCGCAGTGAGTACCACCCACCTGTCTACAGAGCAGCTGGCCGCGCGCTGGGGCGTTACCGTCGACACGATCGAACGGTGGCGATCCGAAGGCATCGGCCCGCGCTACATCAAAGTAACCCGCGCCATCCGCTATCGTCTGAGCGATGTCGAAGCCTTCGAGGATGTCTCGGTGCGATCACCCGAGGACACCTCGGCATCCACGGGAGCGCGAGCATGAGCCTCCTGCAACGCAGCGTGGACCGCTCGGCCACTGAACTGGCCGCATATGCGCCGGAGATGCTGCTTGACCTGAAGCGCGAGGCAACCGAGGCATTGGCCACCGCCAAGGCGCATGCCGACCTGGTCGACCAAGCACTGGCGCTGAAGTACAGCCAGATCGCTCAGGCGCAGCGCTTAGCCGCAGGAAAAGATGCTGGCTCGGTCACCTTCAACGATGGCCCGATCCGGATCAGTGTCGAACTGCCGAAGAAGGTCGAATGGGATCAGACCGTACTCTCGCGCATCGTCTCCCGCATCCAAGCAGCAGGCGAAGACCCTTCGGAGTTTGTCGAGGTCACTTACAGGATCAGTGAGAGCAAGTACAACGCTTGGCCCGCATCCATGCGCGCGACCTTTGATGCTGCTCGAACCCTCAAAGTCGGCAAAGCCACCTTCCGACTGTCGCTGCCGGGAGAGACCGCGTGAGCGGGTTTCCAATCATTACCGCCGATCAGCGGCTGGCAGAAACCCGCGGCGTCAAAGGCGTACTCGTCGGTCGCTGGGGCTTGGGTAAGACCTATCAGCTGTGGACGCTCGATCCGGGCAGCACTTTGTTCATCGACATCGAGGCGGGCGATTTGGCGGTGAAGGACTGGCCGGGTGACAGCTTGCGCCCCCGGACCTGGGAGGAATGCCGCGACATCGCCGTTCTCCTCGGCGGTCCAAACCCCGCGTTGCGCGATGGTCAGCCTTTTAGCCCGTGGCACTTCAACGAGGCGCGTCAGCGATTCGGCGATCCCGCTGAGCTGGCCAAGTACCGGACCCTCTTTATCGATTCGATCACCGTCGCCGGTCGGCTTTGCTTGCAGTGGTGCAAAGGCCAGCCACAGGCATTCTCCGACCGCACCAACAAGCCCGATACCCGCGGCGCCTACGGCTTGATGGGTCAAGAGATGGTTGCGTGGCTCACCCATATCCAGCACAGCCGCGACAAGCACGTCTGGTTCGTGGGCATCCTCGATGAGCGCACCGACGACTTCAACCGCAAGGTCTACGAGTTGCAGATCGACGGCTCCAAGACAGGGCTGGAGTTGCCCGGCATCGTGGACGAGGTGATCACGCTGGCGGAGATCGCGCCGAGCGACGGCGCCCCGTATCGCGCCTTCATTTGCCACACCGGCAATCCGTGGGGCTTCCCCGCCAAGGATCGCTCCGGCCGTCTCGACATGGTCGAGCCACCGGATCTGGGCCGGCTCATGCGCAAGCTCGGCGCCCCCGAAGCCGCCGCCCCCGACAAAACTTCACCCGAATAATCCGCAGGAATCCCATGTCCACCTGGAACAACTTCAACGATGCCGAGAACCCGGCGTTCTCGCTCATTCCCAAGGGCACGCTGGTCAAGGTCCGCATGACCATCAAGCCCGGCGGCTACAACGACGCCAATCAAGGTTGGCTGCATGGCTGGGCCACACGCGGCGATACCGGTGCTGTCTACCTCAACGGCGAGTTCGTCGTGATGGAAGGCAAGTACGCCCGCCGCAAGCTGTGGTCGTTGATTGGCCTGTACAGCGCGAAGGGACCGACCTGGGGTCAGATGGGGCGCAGCTTCATCAAGGGTGCCCTCAATTCAGCACTGGGCCTGCACCCGGACGACATGGGCGCGACCGCTCAGGCCGGGCGCTGCATCAGCAGCTTCGGCGATCTGGACGGCCTGATCTTCGCCGCCCAAGTCGACTGGGAGAAGGACGGTTACGGCCAGGACAAGGCGGTGATCAAGATGCCGATCATGCCCGACCACCCGCAGTACAAAGAGGTGATGGGTGCCGGCTCCGCAGCGTCGAGCGCGTCCTCGGCGGTATCGGCCGCTGTCCCGGCACTCGTCGCGCAGGCAGCGCAAACGGCGGCCCACGCCGGCCCCGTGGCCGGTCGGCCAACATGGGCGCAGTGAGGCGCGCGCCATGCCCACGAACACCAAGCTGCAAGACCTGTATCCGAACCGCAACGGCATCTACACGCCGTTGCGAAAACTCACCAGCGCTGAAGTCGAGGACCAGATCGAAGCGTGCCAGCGTTTGACGCAGCACCATCTCGATCACGCCGAGGCGTTGATCGCTTATCGCGACCGCGTCTTGGATAAGTCTCGTCATGGCCGATGACGTGCTGCTGGGCCTGCGGAAAGCCCGCCCGCGGCTTCGGCCATCTGGACCTGCGCCGCCGGATCGGTGATCCGCGGCGCACACCGTATCGCTGGGCGTTCTGTACGGCCACCTGCCAGAACGCATTCCATCAACTCTACGACACCCGATGCCGGAGCGATCCGGCGTCGGTAGAGGAGCTATTGCCTGTGACACACCCACTGACCCATGACGCACAACGCGCTTGCTTAAAGGCGCTGGCGTCTGTCGCCGATCGCATCGGGTTCGATGTTCCGCTCGCGCAGTACAACCAAGCGCAAGCCACCCAAGTGGTCGACGCCATCACCCAAGCCTACGAATCTGCGATTCGCGAGAAGTCGAGTCGGGCCGGCTACAAGGTCGTGCCGCCGCTCGACGGATTCGAAAACGACACTATTCCTTTTTGATTTTGGCATGCCTTTTTCTATTTTGGCATTTGCAACATTTCGCGTCGCAAATATGCTTGATTTCAATTCCCACGATCTGTCCGAACACCTGAGCGCGTTGGTCGATACCGCCATGGAGCGCGAGGCGGCGATGTTGCCGCCCCGCGCATACCTCGGCGCATCCAGTCTCGGTGACGACTGCGCGCGCCGTTTACAATTCCAATACTTCGACACGCCCAAGGACATCGGCCGGCATTTTCCAGGCCGTGTCCTTCGGGTATTCGCGCGCGGCCATCGAGTCGAGGACTGGATGGCCGACTGGCTGCGCCTGGCCGGCTTCGATCTGCGTGCCCGCAATGACCAGGGCGAGCAACATGGCTTCGCTGCCGCTCAGGGCCGGGTGCGCGGTCATGCCGATGGCGTCATCGTCGCCGGTCCCGACAGCTTTCGTTATCCGATGTTGTGGGAAAACAAAGCAGTCGGTGCCAAGACCTTCCGGGAGTTGCGGAAGAAACGACTCGCGGCCAGCAGGCCGGTCTACGCCACGCAGGTCGCGCTCTACCAAGCCTATCTTGGCCTGTACGAACATCCGGCACTGTTCACGGCGATCTGCACCGACGATATGTCGATCTACGCCGAGCGCGTGACTTTCGATCGCGGTATGGCGCAGCGCGCGTCGGACCGCGCGGTCGAGATCCTGCGCGCCTGCGACGCCGCCGAACTCCTTCCCCGCATCAGCACCACCCCCACCCATCACACCTGTCGGTTCTGCCCTTGGCAAGACCGCTGCTGGAGTCTGCCCCATTGAATACCTGGAACAACTTCAACGATGCATCACCCCCGAGCGTAGGCGGGCCGCCGGCAAGCCGCCACCGGGAAGAGACGCGCACCGCGCTGCTGCAACGATTGCAGTCGGTATTGACGGCCCTGTTCCCGAAGGGCAAAGCGCGCCGCGGCAAATTCACGGTCGGCGATGTCGCTGGCACAGTTGGCGACAGCCTGGAGGTCGAGTTGGCCGGCGACAAGGCCGGGCTATGGAAGGACCATGCCAGCGGCGAGGGCGGCGATGTGTTCGATCTGATTGCCGCTCACCACGGGCTCGATGCGCGGCGTGATTTTGCCAAGGTGCTCGATCAGGCGGATGCGCTGCTCGGCCTGGCGCCGCAATCGCCGGTGCCGTCGAGGTCCAAGCGATCCGAACCGGCGATGGACGACTTGGGGCCGCATACCGCGCGCTGGGATTACCTGACACCGGAAGGCGAGTTGATCGGCTGTGTGTACCGGTACGATCCGCCGGGGGGTAAGCAATACCGCCCCTGGGATGCGAAGCGCCGCAAACACCAAGCGCCCACGCCGCGACCGCTGTACAACCAGCCTGGGTTGGCCGCGTCGAATGAAGCGATCTTGGTCGAAGGCGAGAAAAGCGCCGATGCGTTGGTCGCGTTAGGCGTATGCGCTACGACGGCCATGAACGGCGCCAGCGCACCGATCGACAAAACCGATTGGTCGCCACTTTGCGGAAAGCACATCCTGATCTGGCCCGACAAGGATAAGCCTGGTTGGGAATACGCCATGCAAGCCGCACAGGCGGCATTCCAGGCCGGCGCGGAATCGTGCGCACTGCTGCATCTTCCCGAGGACAAGCCGGAAGGTTGGGATGCTTACGACGCGGTGGCCGAGGGCTTCGATGTGGAAGGCTTCTTGCGTGCCGGCGAGCGCACGTTCCTGCAGCCCGGCACCGATGACGCGCCGCCGCCGATCGACTTCGCCGGCCTGGACTGGAGCAGCGACGACGGTTTGGGTTTGGCGTTCACCCGGCGCTACGGCGACGACTGGCGTTACTGCGCGGCTTGGGGTCAGTGGCTCAGTTGGACCGGGACGCGTTGGAACCCGGATCGGACGTTGGTTCAACAACATCTGGTGCGCGGTGTCTGCCGTGCGGCGCAGGAATTCGCCGATCGGCCGACGCAGCGGTCCAAGCTGGCGTCGGCTTCAACCGTCGGTGGCGTTGAGCGGCTGACCCGTAGCGATCCGCGGCACGCGTCTTCGGCCGAAACCTGGGACAGCGACTTGTGGTCTTTGAATACGCCGCGCGGCATCGTCGACCTGCGCTCTGGCGCTGTGCGCCGGCACGCCCGTGGCGAGCACATGACCAAACTCACGACGGCCAGTCCGGGGGGCGATTGCCCGATCTGGCAGCGCTTTCTGGCCGACATTACCGGCAGCGATATCGCCTTGATTGACTACTTGCAATGCGTAGTTGGCTACTGTTTGACCGGGGTCACGCGAGAGCATGCGCTGTTTTTCCTCTACGGCACCGGGGCGAATGGCAAGTCGGTGTTCGTAAACGTTCTCGCCACCATTCTGGGCGATTACGCGACGAACGCGCCGATGGACACGTTCATGGAGGCGCGTCACGACCGCCATCCGACCGAGCTGGCCGGACTGCGCGGTGCGCGCTTTGTCGCGGCAAGCGAAACCGAGCAGGGCCGACGTTGGAACGAGTCGAAGCTCAAGGCGATCACCGGCGGCGACGCGATCAGCGCGCGCTTCATGCGACAGGATTTCTTCGAATATCGGCCACAGTTCAAGCTGGTGATCGCGGGCAACCATAAGCCGGCCATTCGAAACGTTGATGAGGCAATGAAACGGCGCCTGCATCTGGTGCCGTTCACCGTCACCATCCCGCCAGAAGGGCGCGATGCGCGGCTCACCGAGAAACTCCTGGCCGAACGCGACGGAATCATGGCGTGGGCGATTGAGGGTTGCCTGCGATGGCAGCGCCACGGCTTGCGTGCGCCGCAGTCCGTGATCGACGCGACCGACGAATACTTCGAAGGCGAAGACGCGCTCGGCCACTGGATCGAGGAGCGGTGTTTCGTGCATGACCAGTCCAGGGCTTTGGTCGCCGAATTGTTCGGCGACTGGCGAGATTGGGCTGAGAGCAATGGCGAGTTCGCCGGATCGGTCAAGCGCTTCTCCGACCTGCTCACGGGACGGCAGTTCGCCAAGCACAAAGGTGCAAAAGGGGCGCGGTATTTCCTCGGGCTGAGTCTGAAGCCCAAATCGTTCCAGCAATTCGGAGGTGCGAGCCATGAATGAAATCAATGATTTGGAAGGGCGGGTGGCGGACGAGGCTCGGCTGCCTATTCCTCCTTATGTATGTGTACGCGCGCACGTATATGGACAAATAGGCAATCGTGCCTCGTCTGCCACCCAACTCGCCGCGGATGATCCCCGAGTCGTGCTCACGCTTGATCTGGGCTCTACTCTGGGCTGGGCGTTGAGCATCTCCGGCCAGGCCATGAGCGGCACCGAGTCGTTCAAGCTGAGGCGCTTCGAAGGCGGCGGCATGCGTTATCTGCGCTTCGTCCGCTGGCTCGATGATCTCATGCGCTTCACCGGTCCCATCTCGACGGTGTATTTCGAAGAAGTGCGCCGCCACAAGGGCGTGGACGCCGCGCACGCCTACGGCGGCTTCATGGCCCAGCTCACGGCGTGGTGCGAGCGTCATGCGGTCCCGTATCAGGGCGTTCCCGTCGGCACGATCAAGAAGTTCGCCACGGGCAAAGGCAACGCCAACAAGGAAGCCATGATCGACGCGGCGAAACGGTGGGGCCATACACCCACCGACGACAACGAAGCCGATGCGCTCGCTTTGCTGCACTGGTCCATGGCGCACGGGGTGATGGCATGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP011130|5862467:5871198|5867093_5867522_+|WP_148650608.1|DBSCAN-SWA
MTCCWACGKPARGFGHLDLRRRIGDPRRTPYRWAFCTATCQNAFHQLYDTRCRSDPASVEELLPVTHPLTHDAQRACLKALASVADRIGFDVPLAQYNQAQATQVVDAITQAYESAIREKSSRAGYKVVPPLDGFENDTIPF
>NZ_CP011130|5862467:5871198|5864956_5865427_+|WP_057923031.1|DBSCAN-SWA
MSLLQRSVDRSATELAAYAPEMLLDLKREATEALATAKAHADLVDQALALKYSQIAQAQRLAAGKDAGSVTFNDGPIRISVELPKKVEWDQTVLSRIVSRIQAAGEDPSEFVEVTYRISESKYNAWPASMRATFDAARTLKVGKATFRLSLPGETA
>NZ_CP011130|5862467:5871198|5864747_5864960_+|WP_082648777.1|DBSCAN-SWA
MSTTHLSTEQLAARWGVTVDTIERWRSEGIGPRYIKVTRAIRYRLSDVEAFEDVSVRSPEDTSASTGARA
>NZ_CP011130|5862467:5871198|5864256_5864436_-|WP_148650607.1|DBSCAN-SWA
MNNGLVLRHTLTATLSAPYTNYFLPGTASGIPDRDCGHVFERVICKQQGMHLQSASPIR
>NZ_CP011130|5862467:5871198|5870745_5871198_+|WP_057923037.1|DBSCAN-SWA
MLTLDLGSTLGWALSISGQAMSGTESFKLRRFEGGGMRYLRFVRWLDDLMRFTGPISTVYFEEVRRHKGVDAAHAYGGFMAQLTAWCERHAVPYQGVPVGTIKKFATGKGNANKEAMIDAAKRWGHTPTDDNEADALALLHWSMAHGVMA
>NZ_CP011130|5862467:5871198|5866899_5867097_+|WP_057923034.1|DBSCAN-SWA
MPTNTKLQDLYPNRNGIYTPLRKLTSAEVEDQIEACQRLTQHHLDHAEALIAYRDRVLDKSRHGR
>NZ_CP011130|5862467:5871198|5862467_5862947_-|WP_187313284.1|DBSCAN-SWA
MSSSSSEEAASTAAQVAALPDMPWSQLKARWIALFGEPPGINNRRYVVRRLAHRIQEDAYRISQPSLISENERRVKQLLDTGRVSRRKTQVAPLVGSVLTRVHNGQVHRVKVLDGDVFEYQGRTFGSLSKVAREITGTRWSGPAFFGLRSNHDKKEQGA
>NZ_CP011130|5862467:5871198|5868305_5870603_+|WP_057923036.1|DBSCAN-SWA
MNTWNNFNDASPPSVGGPPASRHREETRTALLQRLQSVLTALFPKGKARRGKFTVGDVAGTVGDSLEVELAGDKAGLWKDHASGEGGDVFDLIAAHHGLDARRDFAKVLDQADALLGLAPQSPVPSRSKRSEPAMDDLGPHTARWDYLTPEGELIGCVYRYDPPGGKQYRPWDAKRRKHQAPTPRPLYNQPGLAASNEAILVEGEKSADALVALGVCATTAMNGASAPIDKTDWSPLCGKHILIWPDKDKPGWEYAMQAAQAAFQAGAESCALLHLPEDKPEGWDAYDAVAEGFDVEGFLRAGERTFLQPGTDDAPPPIDFAGLDWSSDDGLGLAFTRRYGDDWRYCAAWGQWLSWTGTRWNPDRTLVQQHLVRGVCRAAQEFADRPTQRSKLASASTVGGVERLTRSDPRHASSAETWDSDLWSLNTPRGIVDLRSGAVRRHARGEHMTKLTTASPGGDCPIWQRFLADITGSDIALIDYLQCVVGYCLTGVTREHALFFLYGTGANGKSVFVNVLATILGDYATNAPMDTFMEARHDRHPTELAGLRGARFVAASETEQGRRWNESKLKAITGGDAISARFMRQDFFEYRPQFKLVIAGNHKPAIRNVDEAMKRRLHLVPFTVTIPPEGRDARLTEKLLAERDGIMAWAIEGCLRWQRHGLRAPQSVIDATDEYFEGEDALGHWIEERCFVHDQSRALVAELFGDWRDWAESNGEFAGSVKRFSDLLTGRQFAKHKGAKGARYFLGLSLKPKSFQQFGGASHE
>NZ_CP011130|5862467:5871198|5865423_5866254_+|WP_057923032.1|DBSCAN-SWA
MSGFPIITADQRLAETRGVKGVLVGRWGLGKTYQLWTLDPGSTLFIDIEAGDLAVKDWPGDSLRPRTWEECRDIAVLLGGPNPALRDGQPFSPWHFNEARQRFGDPAELAKYRTLFIDSITVAGRLCLQWCKGQPQAFSDRTNKPDTRGAYGLMGQEMVAWLTHIQHSRDKHVWFVGILDERTDDFNRKVYELQIDGSKTGLELPGIVDEVITLAEIAPSDGAPYRAFICHTGNPWGFPAKDRSGRLDMVEPPDLGRLMRKLGAPEAAAPDKTSPE
>NZ_CP011130|5862467:5871198|5866268_5866889_+|WP_057923033.1|DBSCAN-SWA
MSTWNNFNDAENPAFSLIPKGTLVKVRMTIKPGGYNDANQGWLHGWATRGDTGAVYLNGEFVVMEGKYARRKLWSLIGLYSAKGPTWGQMGRSFIKGALNSALGLHPDDMGATAQAGRCISSFGDLDGLIFAAQVDWEKDGYGQDKAVIKMPIMPDHPQYKEVMGAGSAASSASSAVSAAVPALVAQAAQTAAHAGPVAGRPTWAQ
>NZ_CP011130|5862467:5871198|5867574_5868309_+|WP_057923035.1|DBSCAN-SWA
MLDFNSHDLSEHLSALVDTAMEREAAMLPPRAYLGASSLGDDCARRLQFQYFDTPKDIGRHFPGRVLRVFARGHRVEDWMADWLRLAGFDLRARNDQGEQHGFAAAQGRVRGHADGVIVAGPDSFRYPMLWENKAVGAKTFRELRKKRLAASRPVYATQVALYQAYLGLYEHPALFTAICTDDMSIYAERVTFDRGMAQRASDRAVEILRACDAAELLPRISTTPTHHTCRFCPWQDRCWSLPH
>NZ_CP011130|5862467:5871198|5863102_5864107_-|WP_148650606.1|DBSCAN-SWA
MLRNYLHRFETEPVGALLPSSGGGLQSALIDLGAMHPAKRAVRWTCKACRFVDTRQVYSYSDHALRCGVCGGEVDTWPAFQAAQVRHEWLPKVLSEAMAGDGARAIELLPYRLWRLAMLPTASGSVSIYLLRCGWHVEYEPVVRALVDEEAASQMVLTTSKVLTRDISDSSRMVVPLIQVAKLEPQGLLLDLDRLGGLVVPAISVQMRPRDDNLWFDVSADGSRLRMNGQDLFLYRKQRDFILALAEAHASGHRRPKLEWVLRRAKYKGQVTSPRQICARDDFARFIEWNNGEVAVRDEVLPKNVADPNRVSPSRRRSARSERETVKSRHPIDS

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_187313284.1|5862467_5862947_-	DUF2924 domain-containing protein	Q9JML2	Wolbachia_phage	1.7e-08	29.5
WP_148650606.1|5863102_5864107_-	hypothetical protein	NA	NA	NA	NA
WP_148650607.1|5864256_5864436_-	hypothetical protein	NA	NA	NA	NA
WP_082648777.1|5864747_5864960_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_057923031.1|5864956_5865427_+	hypothetical protein	K4HZ96	Acidithiobacillus_phage	8.1e-27	45.8
WP_057923032.1|5865423_5866254_+	ATP-binding protein	K4HZX9	Acidithiobacillus_phage	8.2e-99	62.9
WP_057923033.1|5866268_5866889_+	hypothetical protein	K4ICM8	Acidithiobacillus_phage	1.1e-47	61.2
WP_057923034.1|5866899_5867097_+	hypothetical protein	NA	NA	NA	NA
WP_148650608.1|5867093_5867522_+	hypothetical protein	K4I3X7	Acidithiobacillus_phage	7.9e-21	40.3
WP_057923035.1|5867574_5868309_+	hypothetical protein	K4HZA0	Acidithiobacillus_phage	2.9e-79	59.8
WP_057923036.1|5868305_5870603_+	hypothetical protein	K4HZY1	Acidithiobacillus_phage	6.7e-284	63.5
WP_057923037.1|5870745_5871198_+	hypothetical protein	K4ICN3	Acidithiobacillus_phage	8.5e-50	66.2

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP011130|5880788:5924616|DBSCAN-SWA
CGTGGGAATCTCTATCCGAGCCTACGGCCGCCATCGCGGCGTGTCCGACACCGCTGTGCGCAAAGCCATCGCAGCCGGCCGCATCACCGCCGAGGCGGACGGCACCATAAACGCGGCGCGCGCCGACGCCGAATGGGCCGCCAGTACCCGCGCGCCGGACGCGCCCCTAGCGGCGACAACGCGGCCAGCGCGTGCGCGCGCGGTCAACGGCCCACCGGTAGACGACGTCGGCACCGTGACGCCGGCCAGCGCGGCGGGTGGCGGCAACACCTACGCGCAGGCTCGCACCGCCAACGAGGTGCTGAAGGCACAGCACCACAAGCTGCGCATCGCCCAACTGAAGGGCGAGTTGGTCGACCGCTCCCAGGTGATGGCGCAGGTGTTCGCGCTGGCGCGCGCTGAGCGCGATGCCTGGTTGAACTGGCCGGCGCGCATCAGTTCGATGCTCGCGGCCGAACTGAACATTGATCCGCATGTCATGCACGTCGCGCTGGAGCGCGGCGTTCGCCAGCACTTGGCCGAACTCGGCGACTTCAACGCACGATTGGATTAACCCTTGTACGACGGCTTTGACGACGTTGCGCGGTTCTGGCGCGACGGCCTGACGCCCGATCCATTTCTCGACGTGTCCGATTGGGCGGATCGTGACCGGGTGCTGTCCAGCACCTCGTCGTCGGAGCCCGGCCGCTGGCGCACCGCGCGCACGCCGTACCTGCGCGACATCATGAACGACCTGTCGCCGGCGTCGGCGACCGAGCGCGTCGTCTTCATGAAGGGCGCGCAGGTCGGCGGTACGGAGTGCGGCAACAACTGGATCGGGTACGTCATCGCCTGCGCGCCAGGCCCGATGATGGCCGTGGCGCCCACGGTCGAGATGGCCAAGCGCAACTCGAAACAGCGCATTGATCCGCTGATCGAGGAATCACCGTCGCTGCGCGAGCGCATCGCGCCATCGCGCGCGCGCGATGCCGGCAACACGATCCTCGCCAAAGAGTTCCGCGGCGGCGTGCTGGTGCTGACCGGCGCGAACAGCGCGGTGGGTCTACGCTCGATGCCGGTGCGTTATCTGTTCTTGGACGAGGTGGACGGCTACCCGCGTGACGTCGAAGGCGAAGGTGATGCGGTCGCGCTGGCGGAAGCCCGTACCCGAACGTTCACCCGCCGCAAGATCCTGCTGGTTTCGACGCCAACCATTGCCGGCGCCAGCACCATCGAGCGCGAGTACCTCGCGTCCGACCAGCGACGGTACTTCGTGCCGTGTCCGCATTGCGCCGAGATGCAGTGGCTGCGGTTTGAGCAACTGCGATGGACTTGGGGAGATTCTCGTTCCGCGCGATATATCTGCGAGGGTTGCGAGCAGCCGATCGGCGAGCACCATAAGACCGCGATGTTGGCCGGCGGCGAATGGCGGGCTACGGCGCCGCAGAACAAAGGCAAGACAGCCGGCTACCACCTTTCGTCCTTGTACTCGCCGGTCGGCTGGCGCAGTTGGGCCGACATCGCCGCCGCGTGGGAATCAGCGCAGGGTTCGGCGACGGCGCTGAAGGCATTCAAGAACACCGAGCTGGGCGAGACCTGGGAAGAAGAAGGCGAAGCCCCGGATTGGGAGCGCTTGCAGGAGCGGCGCGAGGATTACCGCGTTGGGACGGTGCCTGCTGGCGGACTGTTGCTGGCCGGCGGCGCAGACATTCAGAAGGACCGCATCGAGGTATCGGTGTGGGCGTTCGGCCGGGGCCGCGAAACGTGGCTGGTCGAGCATCGCGTCTTGATGGGCGACACCGCGCGTGCTGCGGTGTGGAACGAATTGGGCGCGGTCCTGTCGCAGCACTGGACCCACGCCAGCGGTGCGTTGTTGCCGCTCACCCGCATGGGCCTGGACACCGGTTACGCGACGCAGGAAGCCTATGCGTTCGCTCGCGGTGTTCAAGATCCACGCCTGCTGCCTATGAAGGGCGTCGGCAGTGGCGCGGCGCTGATCGGCACGCCGACCGCGGTCGATGTCAGCGTGCCGGGCAAGCGCATCCGACGCGGTCTGAAGTTGTTCGCCGTGGCCGGCGGCATTGCCAAGCTGGAGTTTTACAACGCCCTGCGGCTACCGATCGAAATCGGCCCGGACGGGCAGCCGGCGTTCCCCGCTGGCTATGTGCATCTGCCGAAGATCGATGGCGAGTTCTTGCAGCAATTGACCGCCGAACACCTGATCACCCGTCGCGATCGCCACGGTTACCCGCAGCGCGTTTGGGAGAAGCGCCGCGACCGTAACGAGGCACTGGACTGCTACGTCATGGCGCGCGCTGCCGCGATGCAGGCCGGCGTCGATCGCTTCGAGGAGCGCCACTGGCGTGAGTTGGAGCGAACGCTGGGTATGCAGCCCAACGAACCGCCGGCCATTCCCCGCCAGCCACCGCCGTATCCCACCCCACAGGCCGCCCCACTGGGCGGCCTTTCTGTTTCTGACCCACGCCGTGTGCGCCGGGTCATTTCGAGCCGTTTCATGCGATGACCGATCTTCCCTATACCTACGAGCAGCTGAAAGCGCTACGCAACGCGCTCGCGCGCGGCGAACGCCGTGTCAGTTTCGGCGACCGCTTGGTCGAGTACCGCAGCGTCGATGAATTGCTGGCCGCGATCCGCGAGATCGAAGCGGCCCTGGCCGGCACCGAAGGCCAACCGCGGCGCCCGCGCCGACTGTTGACCACCACCGGCAAGGGCTTCTGATGAGTTGGTGGTCGCGCGTCCGAACCGCGATGTTCGGCGGCTCGCCTGTGCATGAGGTCGCAGGTCACGGCCGGCGGTCGACAGCATGGCAACCCAGCAATCCCGGTGCGATCGCCGCACTCGTAGCGACCGGCGATGCGTTGCGCGTTCGCTCGCGCGATCTGGTTCGCCGCAATGCCTGGGCGAATGCAGCGATCGAGGCGTTCGTCGCCAATGCAGTCGGCACCGGCATCAAGCCGCAGTCGCTGATTGCCGACCAAACCCAGCGCGAAGCGTTGCACGCGCTGTGGCGCGACTTCGTGGACGAGGCCGACGCCGCCGGGCTGACCGATCTGTATGGCTTGCAGGCGCTGGGATGCCGTGCGCTGCTGGAAGGCGGCGAGTGTCTGGTGCGGTTGCGCCCGCGTCGCCCCGAGGACGGCCTGGCCGTGCCGCTGCAACTGCAAGTACTGGAACCCGAGCATTTGCCGCTGACGCTCAACCGCGAGGAACCCAACGGCAACGTCATCCGCGCCGGCATAGAGTTCAATCGGTTGGGCCGGCGGGTCGCGTACCACCTCTACCTATCCCACCCGCAAGACGGCTCGATGGCGCCGATGAGCCGGCAGGGTGGACTGGACACCTTCCGTGTTCCCGCCACCGAGGTGCTGCACATCTTCCGGCCACTGCGCCCGGGGCAAATCCGCGGCGAGCCGTGGCTGGCGCGCGCGCTGGTCAAGCTGAACGAGCTGGACCAGTACGACGATGCCGAGCTCGTGCGCAAGAAGACGGCGGCCATGTTCGCCGGCTTCATTACCCGCGATGGCCCGGAAGACCCGCTGCCGGGCGACGCACCACCGGACGAACACGGCAACGCACCGCTCGGCCTGGAGCCGGGCAGTCTGCAAATCTTGGAGGCCGGCGAGAGCGTTACGTTCGCTCAGCCGGCCGATGTCGGCGCGAGCTACGACGCCTTCCTTCGGTCGCAGTTCCGTGCAGTCGCTGCCGCGATGGGCATCACCTACGAGCAGTTGACCGGCGATCTGACCGGCGTGAACTACTCGTCCATTCGCGCCGGGTTGCTCGAGTTCCGGCGCCGCTGCGAGATGGTCCAGCACTCGGTGCTGGTGTTCCAGCTGTGCCGCCCGATCTGGAATGCGTTCGTCGACGCCGCGGTGTTGTCGGGTGCGATCGAGTTGACCGGCTACCGGCGCCGTAAGCGCCAGTACCGCGCATGCAAGTGGGTGCCTCAAGGTTGGAGTTGGGTGGACCCGGAGAAAGAGTTCAACGCGATGATCCTGGCGATCCGCGCGGGTTTGCTCTCCCGCTCGGAGGCCATTGCCAGCTCCGGCTACGACGCCGAGACCATTGATCGCGAAATCGCGGCGGACGCCCAACGTGCCGATGCGCTCGGCTTGGTGCTCGACACCGATCCCCGCGCCGTCGCCCGCAATGGCGTCAAGCACGCACCACCCCAGGCCGACTCTGCGGCCTTTGATACGAAGCCTACCGAATGACCGGACTGCCCCACCTGGCGGCGCGCGTGTTCAACACGCCGCTGCTGATTCAACGCGCCAAATTGGAAGTCATCCTGAGCGTGCTCGCTCCGAAGTTCGAACTGCAAACGTTGCCACCGCCGCAGATGGGGCCGCCGATGCCCGCCCCGGCGTTGGCGAACGAACAAGGCATCTATGTGTTGCCAATCCACGGCACCTTAGTCCAAAGGGCGGTCGGGTTGGACGCGCTGTCTGGCCTGACCAGCTATGTCTCGATCGCGCGCCGGCTAGATGCGGCATTAGCCGACGACTCCGTGCGCGGCATCGTCTTGGAGATCGACAGTCCCGGCGGCGAGGCCGCCGGCGTGTTTGATCTGGCCGACAAGATCCGCGCGGCAAGCGCCGCCAAGCCGATCTGGGCCGTCGCCAACGACGCCGCATTCTCAGCCGCGTATGCGTTGGCGAGTGCTACCAACCGACTGTTCGTTACCAGAACGGGCGGCATCGGTTCGATTGGTGTCATTGCGCTGCACGTTGACCAATCGCAGTCGGATGCGAATGCGGGGCTGAAGTTCACGCCGATCCACGCGGGCGCGCGCAAGAACGACGGCACGCCGCATGAGCCGTTGACCGATGAGGCCCGCGGCTCGATCCAAACCGAGGTCAACCGCCTCTACGAACTGTTTGTCCTGACTGTTGCCGACCAGCGTGGCTTGAGCGCCGAAGCGGTGCGCAAGACCGAGGCCGCGCTGTACTTCGGTCAGGACGCCATCAACGTCGGCTTGGCCGACCGCCTCGGCACGCTCAGTGATGCCGTGCAGCAGATGCATACCGAACTTGACGCCGCAGCGCGTCCGCTTTTCTTGGAGAACCCCACGATGTCCCTACCTGACGCCACGGTGCCCACCGTGGACACCGACGCCGTGCGCGCACAATCGCGCGCCGATTCCTTGGCGATTGCCGAGTTGTGCGAGCTGGCCGGTCAGCCGCAGTTGACCGCGGCCCTGCTCGCCGAAGGCGTAACGCCAGCGGTCGCGCGCCAGCGCCTGCTCGCGGCCAAGGCCGAGTCCACCGAGATCACCAGCCACTTGTCGCCGAACGCCCCTACCCCGTCGATGGCGACCTCGCTGGACGACAACCCGCTCGTCCAAGCGGTCAAGGCGCGCGCCGCCGCTACGCGAAAGGAACGCTGAAATGCGAATCACCACTTACCCGCCCTTCCAAGAGGGCTTGAACCTGGGCGATTTGCTCAAGTTCGAGGCCGACAACCTGTACTCGCGTGACCAAGTCACTATCGCGCCCAATCAATCGCTCGTGCTGGGCCAGATCGTCGGCCGAGTGAGCGGATCGAACCACGTCGCGGCGTTCGATCCGGCCGCGACCGATGGCCGCGAGATCGCCATCGGCGTGGCCATCGTGCCGATCACGACGACCAAGGACGCCAGCCCTGACGGCCTGATCATCGCGCGCCACGCCGCCGTGGCTGATCACGCACTGGTCTGGTCTGCCGCCATTACCCCCGAGCAACATGCCGCCGCGGTTGAGCAACTGCGCGCGCTAGGCGTCCTCGTGCGCCACGGAGTCTGACCGATGTCGATGAACAACCCGTTCCACAACCCGGCGTTCTCGATGAGCGCGCTGACCACGGCGATCAACATCCTGCCGAACCAATACGGCCGGCTGGATGAGCTGAACCTCTTCCCGATCAAACCGGTCCGCACGCGGCAGGTCACGGTCGAAGAGCGAAACGGCGTCCTGTCGCTGCTGCCGACCCAGCCGGTCGGCTCGCCGGGCACTGTCGGCAAGCGTGGCAAGCGCGCACTGCGCGCGTTCAACGTGCCGCACATTCCGCACGACGACGTCGTGCTGCCCGAGGAAGTAATCGGCGTACGCGCGTTCGGTTCGGAAAGCGAGCTGCAGACGGTTGCCGGCGTCATGGCCGACCACCTGCAGACCATGCGCAATAAGCACGCCATCACCCTGGAGCACCTGCGTATCGGTGCGTTGAAGGGCGTGATTCTTGACGCGGATGGCAGTGAGCTCGCCAACCTGTTCGACATCTTCAACATTGCGCCTAAGACGTTCGACTTTCAGCTGTCCAATCCCAATACGGACATCAAGAAGAAATGTCTGGATTTGAAGCGTTACATGAGCAAGGTGTTGCTCGGTGAGCGAATGACCGGCATTCACGTTCTGGTTTCACCGGAGTTCTTCGACGCATTTACGGGACACGACGCCGTAAAAGATGCCTATCGCTTGTGGCAGGACGGGCTCGTTCTTCGAGAGGACATGCGGTCGGACTTCCGATTTGCCGGAATCCGGTTTGAGGAATACATCGGCGAGGTTAGCGACGGCGAAGGAAAGACGCGGCGTTTCATTGAGGAGGGAGAGGCCCATGCATTCCCCCTTGGCACGATGGACACGTTCGCGACCTATGTCGCCCCGGCCGACTTCAACGAGAGCGTGAACACGTTGGGCCAACTGCTCTACAGCAAGCAGGAGCCGCGCAAGTTCGACCGCGGTACGGACTTGCATACCCAGTCAAACCCGCTACCGATGTGCCACCGACCGGCGCTGCTGCCGAAGCTCAAGATGTGATTCCGTTTGAGCAGATGGATGACGTAATCTTCGCAACGCTCGGCGTCGTCGCGCCTGTAAGGCGTCCGAACGTCTCATCGGCCCGCATCCCTCTTGTAGTGCGCGACGGCGTCGAGCGTCTTGGGGAATTCCAGCAGGTCATTGGCCGCGCACGGCACGTATCCGCTCGAAATCGTGAGTGGATGTTCCGTCGCGGCGATGAAGTCACGCTCGACGGGCGCGTTCAGATCGTCGAAGCGCTCGTAACGGACGACGGCCTCATCAACGAGGCGGTGTTGCATGGCTGAAACAGCGCCGACGTGGCTGTTGCTCCAACGCATCGCTGAGCGGTTGGCTGAGATTCGCTCAGATCGTGGCTACAGGACGGACATCGGCATGTCGGTCGCGCTGGAACCGGCCCAACATCCCGACGAAGAGGCCATTGGCCTGACGCTCGCCTCGCTGGGTATTCAACGCGATGCCAACAAGCCGCATGGCCGGCATCGTCTGCTGCAAGGGCTGGCCGAGGCCACGCTGCCGGCGTCACTGGCCGATGCCCATGCGCAATGCCACGCCATCGCAGCCGACATCGAGGACGCCCTCGATGACTGGATTCCGCTACCCAATGCGTTGCCGGTACAGGTCGAGGACATCGTGTTCCTTGATCGTCCCGAGGGGCTGCCAGTGGTCGCCGTCCAGGTCGCCCTGACGATCCGCTATCGCCGCTGATGGACATCTTCATTGACGCCAATGCCGTGCTGGATACGGCCAAGCGTGTGAGCGAGATCCCAGCCAAGGTTGCGGTGAGCCAAAGGCGCGCGCTGGGCACGTTGCGTCGCCGTTGGCCTGTCATCGCGCGGCGCGATATTCAAGCCGAGTACGCCTTGTCGGCCCAGCGCATCCGAGCCGGCGTCAGCGTGCGGACCACCCGGGAGGGCGTCGAGTTGGTCGGTGTAGCGCGCGGCGTGGGCCTGCGCAACTTCGGCACCCGCAAGACGGAAGATGGCCTGAGCTATTCCGCGCTGCGCGGTAAGCGCGGCTTTCGGCGCAAAGGCTTCGAGAGCCGCTACCGCGGTACGCCGATCGCCTTTGAGCGCACCCCGATCTCCGGGGACAAGCGCGTTCCACGCACTCCGATCCGTCGCCTGTATGGCCCGTCGCTGGCGCAGATGTTGCGCAAAGACGACCGGCCCGAGCGCATGGCCCAAGCGGGCCTGGACGTGATCACCGCCGAGATCGACCGGCTGCTGTTGCGCTCGTTGCGCCGCTGATTCCGCTGCCCACGGGGCAGCCACACCCATATATATGTAGGAGCAACGCGACCGATGGCCGCGCAGGACCTGTTTTCCTTTCAGGGCAAGGTTTACCTCGCCCAGCGCCAATCCAATGGCAAGCCCGGCCCGCTGCGGTGGGTCGGTAACGCACCCCAGCTCCAGCTCACGCTGGAGGTACAAAACTCGGACAAGACCGAGTCGTTCAGCGGCAATCGGATGCTCTACGGCCGTTTGGTCCAGAGCAAGACCGCCAACGTCAACCTGACCCTGGACGAGGCAACCCCGGAGAACATCGCCGAGGGGCTGTACTCGATTCCGGCCACCCTGCCGGCGGGCGCGATCAGCAACGAGTTGCTGCCTCCGGGCCTGAAGGCCAACGACCTGGTCGCACTCGACCGCGGCTGGATCAGCGAACTGTCGCTGACCGACAGCGCGACGCCGCCGGTTACGGTGCCGGCGGCCAACTGGTGGACCGAGTCGCCCTCGGCCGGCGTGATCGGCTTGCGCAAGGTGGATGGCCACACGCAGCCCTTCAAGGCGACCTACCAGCATGGCGAAACGGTCAACATCGCTCTGTTCAATACGCCGCCGCCGGAGCGCATGCTGTTCCTGGACGGCATCAACACGGTCAACGGCCGCCGCGCGAAGGTCACGCTGTACCGAGTGGCGTTCAATCCCATCGAGCAGTTGGATTTGATCTCGGAGGAATGGGGCAGCCTGCAGCTGTCGGGCGCGGCCCTGTTCGATGAGACCCGCGCGTTGGACCCGGCGCTGGGTGGGTTCGGCCGGATAGAAATGGTGAGGGCGTAATGGCGCGCAAAGTCCAACGCCCCAAGCCACCGGCCGACGAACTGACGGTGCTGCAACCGAATCGCATGCTGCCGCTGGGCGATCGCACCGTGACCGTCCGAGAGATCGGTTTCTTCGAAAGCCTGCGCTTGCACGCGCAGATCGCCGCGTTGGTCGCCGACCTGATTGAGCAAACCGACGACGGCAATATTGATCTGGGTCGTCTGCATCGCGTCTGCGCGCAGCACCCGGAGGCGACGGTCGAATTGCTGGCCCAGGCCAGTGATCAATCCGTCGAGTTCGTGCATTCGCTCAGTGCCGCGCACGGCGATCTGTTGCTGCTGACGTTCTGGGCGGTCAACGCCGATTTTTTTCTGCAGCGCGTGATCGCGGCGCTGGAACTGCGTCGCGCGGACCCGGCAACGACTGGCCCAGCGTCCTCGCCACCCTGATCGACCACGGCCACGACTGGCCGTGGATCGAGCGCGCCACCGCGCGCCAACTCGCCTTGTTCTACCGCGTCGCGATCCAGCGCGAGCGCGCACTGCGCGCCGAGCGAATCGAGGACGTCAACGCCGGCTTCGCGGGCGGGCGCGACGTCACCGCCTTTATCCAATCCCTTCGGAAATCCCCATGAAACTGATCGAGAACTGGCGCCAAGCTTGGCGCTTCGTAAGCGTGCAAGCGATGACCGTGGCCATCGCGCTGCAGGGCGTGTGGCTAAACCTGCCCGACGACCTGCGCATCCACGTCCCCGACCGCATCACAGCCACCGTGACCGCCGGCCTGTTGATCCTGGGCCTGATCGGCCGTCTGTTCCAGCAGCGAGGGGCCGATGGCACGACTCTCCGCTGAGCAGGCCGGTGGCCAGAACGTCGTCGCCTTCCTCGACATGATCGCCCACGCCGAGGGCGTAGAGCGCTTCAGCGAGCACGGCGGTTACGACGTATTGGTCGGCGGCAAAACGTTCACCAGCTATGTGGAGCACCCACGCAAGCTCGTCTGGCTGCCGAAATATCGCATCAATTCCACTGCGGCGGGGCGCTATCAGTTCCTGTGGAAAACCTGGAACAGTCTGCGCAATCGTCTGCGACTGCCCGACTTTGGCCCTGCCTCGCAGGACCGCGCCGCGATCGAACTGCTGCGCGAAACCGGCGCACTGGCCGACATCAAGCAGGGCTGGATCAGCAGCGCGGTGCGCAAGTCGCGCAAGACCTGGGCGTCGCTGCCCGACGCCGGCTACGGCCAGCGCGAAGTGCCGCTGGAACGCCTGCTCGCCGTGTACCAGAAGGCGGGAGGCCAGATCGCATGATCGCACTGAAGGTTTGGGCGACGACGCTATTGTCCGCGCTCGCCGCAGTGCTGGTCGCCTTCGGCTGGGGCCGCTGGAAAGGCCGGCAGAGAGAGCGTACCGACACCGCCGCGCGAGTCGCCGAGAGCGAGCAGCGGGTACGTGTCGCCGAACGCGAGCGCGCCGATTCCGAAATCCGCACCGAGGTAGACACCGATGTCCTGCATCTTCCGACAGGCATCTTGGCGCCAGTGGCGGACGCTGTGCCTGATTCCGCTGCTGACCGCCTGTACGACGACTGGTCGCGTGACGGAAGCAACGACGGGTTGCGCCTGGACGCGGCCGATCCTGGTCTCGCGGGAGGATCGACTGACCGATCTGACGGCGCGACAAATCCTGGCGCATAACGAAACCGGTCGCCGACTGTGCGGCTGGGAACCCAACAGGAATTCAACACCGCCTACCAAGGCGACTCAATAGATCGCGCAGGCGACGCGAACGCCTTCGAAAAATCGAAGAAAGTGACGGTATCGGCTAGTTATTCCGGATTTCTCCGCGAGGCGACCGGGAACCGTGACCCTGCGCACCTAGCCTTCCCCTAGTCGTCGCTATTCTCGCGAAACACTCAGGGAGGGAGTTAGATGCGGACCGTTGCGTCGAGATGCTGGTCGAGCCTGCTGCTCATACTGTTGGCGTTGTGCGCCAGCGGTGCTCATGCCGCGTCGCTCCGGCTGGAGCGATTGGACCGGCAGAGTGCCCAGCCGGAGGAGGTCCTAGCCGGCGCCTACGATCAGGAATTCCGTAAGGTCGACGGCCCTAGCATTGTGATCCCGCGTCCTGCGCCTCAATGGTGGCGGGTGGTGCTGGGCGACTTGCCCACAGATCGCGCGCTGCCCCAGTTGGTCCTATCGCCTCCGAATCAGAAGCGCCTGGAAGTTTGGCAGCCCGGTGAGCAGATGCCGATCAGCCGGTCGGCGTTCGGACCCGAGTCCGAGTTGTTGCATTCTGCCCGCGCGCTGGTGGTCCCGCTCAATGCGGGTCTCAAACCCGGCGATGTGGTCTATCTCCGAATCACCTCACCGAATTTGATCGCATCTGAACTGTCGGTCCAACCGATGGCGACAGTGCATGCCGATGACGTCTACTACGCACGATTCCGGGCCTCCGTTCTCGTTGCCCTTTTCATCGTTGCATTGATGTCGTTCGGGTACTTCGCCGCCTTACGCGAACATGGATACGCATACCTCGGTATTACGTTGTTGGCCCAACTCGCCAATCTGGTGATTGAAGGTGGCGAGGTTCGGGTATTTCCCGCATTGGCCGAGTTCGCGATGGACCGGCGCACGAATATCGTCATCAACACTGCGGCGGTGCTAACGGGCATCCGATTCTTGATGTTCTTTCTCCAGCTTCAGATACAGCAGCCGCGCGTCGCAAAATTGCTCAACGTGTGCAGTGTGATGCTGGGCGGGTTGCTGCTGGCTTCGGTGGTCCATGTAACGACGTTCAGTGCCTACTTTGGTAATACCGTCATGCTCGTGGCTTTCGGTGGTATCGCAGTTGCGATCTGCCGGGGGCTGAGACGCCGTCAACTGGACGCGATGTACCTACTGATCGCCTGGGCACCAGTGATGGTCGTGCTGGTTGCGATGGTGGGCGGCTATCAAGACTGGTGGGCGATGCCGGGGTGGGCTATAGACGGGTTCCCCATCGGCGTGGCGGCCAGCGGCTTGGGCTTGATGCTCGGCCTCACCGCGCGACTGGAGCAGGTCCGCGTGGATCGCGACGCAGCCCAGCGGCGCTGGACCTACGACAAGCTCACAGGGGTGATCACGCGCGACGCCGTCGAGGACATGCTGCGGGTCAACATCGAAAAAGCTCACGCGGCTGGGTCGCCTCTATCGGTGGTCTTTGTAGACATCGATCATTTCAAGTCCATCAATGACCTGCATGGCCATTCGACGGGCGACGAAGCGTTGAGGATCGTGGCGCTGCGTATACGAAATTGGCTGCCCGCAGGCCACTTGGTCGCGCGCTATGGCGGCGACGAAATGCTGCTGGTGCTGGTGGGGCTGAATCAGCGCGAGGCGCTGGTGCTGGCGGGTGCGCTACGAGAGACCGTCAGTCGGAATCCGCTGGCGATCGACGGCATCGTCGTGCCCCTCGGTTTATCGATGGGCGTCGCGGACCTGCAGCCGGGGGATTCGTCACAGACGCTACTGCGTCGGGCTGATGCCGCGCTGTATCGGAGCAAGGCTAGCGGCCGTGCCAGGGTGACTGGATACGGCGTCGATGGAGAAATCGAAGGTGCCGGCTAGAGCGATCTGTGAGTGGGATCATGCTCTTCGCCCCATCCTCTGAAGCGGGTTAGTTCGCTCGGGCTACATTGGGATGCGGTGGCCGCCCAAGGCTGGGCAGGCCCGGACCGCATGTCGCCCAACAGAGGACACCGTCATGAAAGCGTGCGCCACCATCGTCCTGGCTTTGATCCTGCTCGTCTGCGCGGGCTGCAAGCCGCCCAATCTGATGCCTCCGGGCGAAACGGCAAGGGCACCGACCCAATCGATCGCCAGCCATCCATCTGCTTGATCGCGTCGCTTCACCTGTACCTCGTTCTGCCGAACCGTTCGATAGATCGGCACCCCTCCGCCGCCTAGGCGGAGGCACTTTCTGCGGCCGTTGCCGCGAATCCCTTCTTTAGCTCCAGTGCTCGGCCGCATTGCGGTGGGGCCGCTGTCGCCCTGCGCGTGTTGAATGACCAATCGCGATACCACGATCACGTTGCTGATCAAGGCCAACGCCACACAACTTAATCAGGCGTTGGAACAAGCGGGAGTGCGCGCCCGAGTCTTTGGTAACGAGGCGGAGAGCGCGGGCCGACGCGCCGGCAAGTCCTTTGATAGTTCGCGCGGCAGTGTCGAGGCCATCGGACGCCAGCTCGGCCAGGCCAAGGCACAGCTGCTGGCCTTCATCGGCCTGCAAAGCGCCGGTACGGCGATCGGCGGCTTGGTGCGTGCGGCAGATGGCTACGCCAACCTGTCGGCCAAGATCAAGCTCGCTACGACATCGCAGGCCAGTTTCAACCTAGCTGAAGACGCCGTCTTCGCGATTTCGCAGCGAACTTCGACGTCGCTCGACACTACTGCGACGCTATTCGGTCGCCTCAGCAGTGCGCTGAAGGACCAGGGCGGCTCGCAGCGTGAAGTGCTCGGCCTGACCGAGACGATCAACAAGGCCCTCGCGGTCTCCGGCGCCACTGGCGCGGAGGCGTCGTCGACGATCCTGCAGTTAAGCCAAGCGTTTGCTTCCGGCACGTTGCGCGGCGACGAGTTCAACTCGGTCAACGACGCCGCACCGCGGCTTATGAAGGCCCTGGCCGCCAGCATGGGCGTGCCGATCGGCGAACTGCGCAAGCTGGCCGAGGCGGGCAAGCTCACCAGCGAGCAGCTGCGTGTCGCCTTCTCCGGTGATCAAGCGAAGAAGATCGCCGCCGAATTCAGCCAACTGCCGCTCACGGTCGAGCGCAGCCTGACCCAGCTCGACAACGCGTTTACGCGGTTCATTGGTCAACAAGACCGCGCCACTGGCGTGTCGACTGCGGTCGCCGGTTCGATCCAAGGGTTGTCGCAGAACTTCGACAGCTTGGCGAATGTGGTCGGCGTGGTGGTCGTGGCCGGGTTGGGTCGTTTGATCGCTACGCTGGCCACGGCCGGCGCCGCGAAAGTGGCCGGCATTCAGAAGACACAGCGGCTGGCGCAGGAAGAATTAGCGCAAGCACGGGCAGCTGAAACCGGCGCGCAGGCCGAACTTGCGCGCGCTCGCGCCCTAGCAATGTCGGGTTCGGGGACTGCGCGGGTCGCTGCTGCCGAAGGTACTCTAGCCGCCGCCCAGGCGAGGACGGCCGCCGCTACGCAGGTGGCGACGGCTGCGGTAGGCGCAAAAGCGGTGGCGGTACGCGCGCTGTCTTCGGTGCTGACCCTAATGGGGGGTCCACTGGGTTTGGCGATTACCGGCGTCACGCTGCTGGCGAGCGCGTTTGCCAGCGCCAGCGCGAATGCCAAAGCAGCCAAGGTCGAATTCGAGAACACGATCAAGGCCGCGCAGCGCTTTCGCGAACAACAAGACATCGATACGGGCGTCGACGCCGGCAAGCGCCTGATCGCGCAGCGAGAGCAACTCCAGAAGGAGCTATCCGATCTTGAAGGCATTCAGAAAGGATGGGGCGGCGGTCACTTTAACGAGGGCCAAAGCTCGGGCCGGATTCTCTACGGCGCGGAACTGGACGGCGAGATCAAACGCGTCCGATCGCAGTTGGCACGAACCAACGATGAGTTCAATCAAGTCCGCGACTCGTTGACCCAACTTCGCGCGGCTCAGGCCAGCGGCGGCCGAACGCGGCAACAAGCAACCAAAGATGTCACTGACTTTACCAAGGCGCTGGCGGACCAGAACGAAAAACTCAAGATCGAGCGAATCGAACGCGAGAAAGGATTGCGCGCGGCGCTGGAGTACCAAGCCGTCAAAGCGGCGGGGGTCAAGGACACCGCGCAACTCACCGAGGCCACGCGCAAGGCCATCGATGAGCAAGTCCGCGAGCGAGACGCGGCCAAAGCTTCGTCCGATGCCGGTCGCGCGCAGGCGAAAGCCGTTCGTGATGCGGAACGTCAGCGTAAAGCCGATGAGCGAAAGTTGCTGCGCGACCAGAAGGAGCAAGAAAGAGCAGGTAAGAAGGACACCAAAGACGATGAAGCACTAAGCCGAACTGTCCAAGAAGCTGACATCGCCCTCATGCGAAACCGCGGCGAGGGTGCGGCGGCTCGCAGGAAGGAGTTGGATCTTGAGTACAAGAAGGCGCTCGCTGATCTGCAGGCGAAGGGCAATACTGCTGACGCGCTCAAGATCCAGCTTCGCATCGATACGGATGTGGCGAAGGTCGAGCTTGAGGATCTGCAGGCACAGGTCGATCACGTGTTCGGCGAGCAGTCCCGGCAAGAGCAGTCGATCCAAACTCGGCAACAGTCAGGTCTGCTGACCGAGGTTGGCGCTCGCCGGGAATTGATTGATCTGCACGCGCGTACCGCCGCCGAGGTCGAGCAGCTGCTTCCGAAAATGGACGCCTTGGCGGCCAAGACTGGCACTCCGGAGTCGATCGAGCGGGTTAAAGATCTGACTGCGCAGGCCGCGGCGCTCACGCTTCAGTCCAATGAACTTGTGGTCACGCTCACCAATGGGTTCGAGAGCGGATTGAGCAACGCGCTGGAAGGATTGGCGACTGGCACGCTGACTCTGCGGCAAGCTCTCACTGGTCTGGTGCAGGACATGGCCCAGTCGCTGGCACAACTAGCCTCCCAGCAACTGGCCGCGCTGGCTACGGCCAAGCTGATGTCTTTGGTGGGAAAGGTCGCCGGTGGGGGTAAGAGCCCTGACGTGGCCCAACCGGACCCCGTCCAGGCCGCTGCGGCTGGCGTCGCTTATGCCACGCCGATTACCGGCGCGTCGGTGGCGCTGGGCGTGGCCGGCGGAATCGTGCTCAAAGCTGCAGCGGCGATGCAAACAGCGGCGGCAACCATGTTGGCGGCCAACGCTTCGAAATCTGCGGCCGGATTCTTCGCCAGTGGCGGCTTCACCGGCATCGGCCCCAAGTACGCCCCAGCCGGTGTCGTGCATCGCGGCGAGTTCGTCCATCGACGCGAAGTCGTTCGACAACCGGGCGCGCGCTCGTTTTTGGAGCGCTTCAACCGCCTGGGCATGTCGGCGCTGGAAGGGTTGCGTGGCTATGCGACGGGCGGATTTGTCAGCCCGGCGCCACGCGCGCCGGCACCGACGCGGGGTCCCATCGCTGACCGCACGGCACCAGCGGCGGAAGGCGAGCGTCGTGGTTCGCAGATTACCAACGTGCTCTATCTCGATCCGCGCGAGATCGTGAACGTCATGAGCACGCAGGCAGGCCGCCAGGTGATCCTGTCCACGATTCGCGCCAATGCCCCCACCGTCCGCCAGGACCTGGGGTGAGTCTGATGCTGCTGGTCTCAACCTGAGCGATGACCACCCGCCACAATCGGCCCAGGCGGGTTGGTCTCTCCCCATTCCCATCTGCCTTGCGTGCCCGGTCCTCATCCGGGCGCGCTTTTTTTGTGCCCATGACTCTTCGTACCGGCGTCGCCAGCGACTACTACGATTTCCTCAACCAACTTGAAGCCGCCTTGTGCCGTGAAGGGCATGCTTGGGGCCTGCTGTATGCCGGTGCCGGCAATGGCGCGTTGACCGGCGTCGACGGCGGTTCAGGCGGCTACCGCGGCGGTACTGGCTCGCTCGCGGAGGCGTTCACCCTGACGGCGCTGGACGCCCAGCGCTTCCAAGTGGTCGGTGCGCTGGCCGGTGATCTCGGCGTCGCCACTGTCGCCCAACCCTTCGAACACGAACGGCTTCGCTTTCGGATCAACGCGGGATCGACGGCCTTCGCGGCCGGTGATCGCTTTACGTTGAACACCTCGCCACCCTGGACCCTGGTGCGCCGATGCGGTGTGCGGAACCCGAGCTTCCGCACGGGCAACTTCACCAACCTGTCCGCGTTGTTCGACAACGCAATGGATACTTGGGCCACGCGCGCAGTGACTGATCTGCCCGCGATTGCGCGAATCGAGATGATCGGCCCAGCCGCCGTCCGTGCGGTCACGATGGGCATCGGCGATTCGGGCGCGCGCGGCGCGGCGGCGTTCGAGCTACAACGCTCCGACGATGGTGCGGCTTGGTCGCCGGTGCAGACGTGGTCCGGTGTGCGGTGGCCCTCGGCGCGCGCGCGACAGACGTTTCTGGTGGCGGGCAACCCGCCTGCCGCCCGATTTTGGCGCGTGGTGTTCTCGGCTACGAACGGCGCGACGCCGCTGGATTGCAATGACCTGTCGTTCCATTTCGACCTCAACGCCGACTTCGAACTGGAGGACCGTGCGCAGTGGATCGTGAAGGCACCCGGCCTGGACGGTCGTCAATCGATCTTCATCGGTGCCGAGCTGTTCGAAGAACCCGCACGCGCGGCGTACAACCTAAATTGGTACGGCTTACGCAGCCACAATCCATTGCTCAGCCTGCGCTCGCAAGTCAACAACAGCGGACTGCGGCATCTGCCGCTGCGCAATGGACCATTTGCTTACTGGCTCGCCATCAACGGCCAGCGCATCGTGATCGTGGCGCGAATCGGCACAGTCTATGTCAGCGCGTACCTGGGCTTTGCGACCGCCTACGAACCGCCCTCGATCCATGAGTACCCGTTGATCATCGGCGCCTGCGGGTCAACCGAGAACGGGACACCCGATGCGACCGACGCGAACTTCCGCGGCTTCTTCGATCCGGGCCGCTATGCGTTGATGGCGAATTACCCCGACAACGTGTGGCGCCCTCATTGCAATCGTTATGCATCGGGTACGAACGATTATGGCGACACCGAGACGGCCGGCAAGGTCTATCCGAGCGCGATGTCCACCGGCGGGGATCGCGCTTATCTGCGCGACAACCTCGATGGCTCATCGCCGCTGTTCCCGCTGATCCTCGGGGCGGCTCAACCGCGCCACGGCTGGGGTGAGTTCGATGGCTGCGCCTGGACGACCGGATTTTCCACCGCATCGGAATCTCGCATCGAACGTGACGGTGCGACGTGGCTGGCGTTCCAGAATGCGTTCCGTATCTCCCCCGACAATTACTTCGCCTTGAAGATGGACTGATGGCTTACGCAACCTCGGCCGCGAATGATCCCAACGAGCTGCTCGACAAGCTGCGCCTGTTCGCACAGAGCGCGGGGTGGTCGATCGACGGGCTACGCGATCGCCCTGCCAATGCAGGAAAGGCGCTCAGCCTGCATGCGGGCAACGTTTACGCGACCTTCGTGTCTCAGCTCGCTGGGGGCGACGGCAACAGTCCAGCCCCCTTTCTCGGCTCGTTCGGCCACACCGGCTACACCGCCAATCCAAACCCGGACATCCAGGCCGATGCGAGCAGCATCGTGTGGGCGAATTATGTCCAGGGACCGTACAGCGCGGTGCATTTCTTCGGTCGCATCGCGCCGCAGCCGTACCTGCACATCGTGCTGGAGACGCAAGCCGGCACCTTTAAGCATTTCGGCACCGGCCGATTGATTACCGCGGGCGTCGTCAACACCGGCCAGTACATTTACGGGAGCCAGTGGTACTACTCGGCGACCTACATCAACAGCCCGGATTCGCCGTATCACAGCGTCGCGTTCGATGACACCTATTACAACTACACCGCGCCGTGTACGCGCATCCGGGCCGACTTTGAGGGCATCGCGCCACGCTGGCATGCGACGAGCGGCGACAGCAACGATTCAAGGCGGTTGTTGGCGGGTTGGCGCGGCAAGACGGCGCCAATCAATCTGCTGAAGGATGTCGGGCACAGTACGCTCACGGGGCGCGCGCCGGGACAGCCGCTGTGGTGTGCGGTACCGCGTGGCGCTGGCCTGTTCTCGGACGTCGGCCATCCCCCCGACATGCGATTCATCCGCTTGGACAGCTACGCACCGGGCGAGGAGTTGCCGCTAGGCACCGATCGGTGGAAGGTCTTTCCCGTCCACCGAAAGAACGGCCCGCCCGGAGCCCCGAATAGCGGTGTCTACGGCTACGCCTACCGCATCAGCGAGTAATCCGACCTCTTCATGATTTGGCCCGCCCTCTGGCCGCTGACCTTCAGCGGTCAGGGCGACTATTTCAAATCGCCGCCGTTCTGGAATGGGCAGGCCAGCGGCGCGCTTGGCGCCGAGCCCGGCTTCGGCCGACGCGCTGTCGACGTGCCCGGCTTTGTGGCCGACCGCCGCGTCGGCGCACCGCAGGCGATGTTTGGCGACGACTTCTTCGATCGTATCCACATCGAGCCGCAGGTGCTCAACCTGGGCAATGTCAGCAGCGTGCAGCAGCGCGCGGTGCGCGTCTGGAATGCGTACCGCGCCCGCGCGCTGACGTTGACCGAGGCCGCCTTGTCGGGCGGCGAAGGCATTGTCCTGACGGCGCCTGGCGCAACGCCGCTGCCGTTCGCGCCGATGTCGGAGCGGACGTGGCAGATCGCGGTCGGCACCGATGGCCCGCCAGTGATCTCCGCGACGCTGTCGTTCCGGTTTGATGGCTTCGCCGCGATTCCGGTCGTCATTACCGGCCAGCGCATCGTCGCCTGGGCGTTCGCGCCGGATTGGTCGCGCGGTGTGCTGGAGCGGCTGGCGTGGAAGACTGACATCCTGACCAGCCCGACGCAGGTCGAGCAGCGGCGCGGCCTGCGCTCGGCGCCACGCCGGTCGTTCGAAGCGACCATGATCGTGGACGGACGCGAGCGGGTGCTTCTCGATCTGGCGGTGTTCGGTTGGGGCGGTCGGACCTGGGCGCTACCGATCTGGCCGGATGTGCAGTGGTTGTCGACCGAACACGCGCTCGGGGTGCGGGTGATTGCCTGCGATCCGCGCCACCGCGATTTCCGCGTCGGCGGTCTGGTGCAACTGCGCGGCAAGACGGCATTCGATGTCGAAGTGGCCGAGGTTGAAGCAATCGGCGGCGCGTCCATCACGCTGCGCCATCCGACGACGATGGCTTGGCCGCTTGGCACCCGCCTGTATCCGGTGCGAACCGCACGATTGGCCGAGCCGCCGAGGGTCACGCGCCTAACCGATCAGGCGGCCTCGGTCAGCGCCCGGTTCGATGTGGTTGAAGCCTGCGACTGGCCGGTCGTTACAGACGCCCCCTTGTACCGCGGTCATCCGGTGCTGGCCCAGCGGCCCGACGAAACCGAATCGTTGTCGAACGGTTGGCAGCGCATGTTACTCACCCTAGACAACGAGTTCGGCCGGCCCTTCGTGCTGGACCCCGCCGATTGGGCTGCACCGACACAATCCCATCAATGGCGCATGCACGGTCGCATCGAGCGGGCGGCGGTTCGGTCCTGGCTGTATACCCTGCGTGGCCGCCAACAGGCAGTCTGGCGACCCACCCACGCGGACGACCTGACCTTGGTCGCCAATGTGGCCGGCACCGCTACGGCGCTGGACGTCGCCAATGTCGGCCTGGCCCGGTTTTCCGGCCTGCGCCTTGGTCGGCGCGACGTGCGGATCGAGTTGCGCGGAGGTCAAGCATTCCATCGCCGGATTACCGCAGCGGTCGCCCTGGATGACGACATCGAGCGCCTGACGATCGATGCCGCGCTCGGCGTGGACATGCGGCCGCGCGATGTGCAGCGCATCAGCTTCCTGGTACTGAGTCGCGGCGACAGCGACGAAGCGGAAATTGAACATCACACCGACAGCGACGGTGCCGCCGACGCTTCCATCATCCTGCGCGCTGTGCGCGATCCCGATACTGACACTCCCGCGCCGGCATGAGCTTCGAACAATTTGAGCGATCGACTGCCGCGGGTAACCCGCGGCGGCTGTACGAGTTCGTGCGCGGCGCAAAGCGCTGGCGCTATACCGGCGGCGACCGCGCCATTGCGCTCGACACGCAGATCTATGACGCCGTCGCCATCAGCGACGATGGCATCCGTCAGTCCGGCCACACCGCCAGCGACATGCTGACGATTACCGCGCCCGGCGATTTCGAGGTCGCGCGCCTGTATCGCGGACTACCGCCATCGGGCGAGATCGCAGTGGTAATTCGCGATATCCATGAAACCGACGACGACGCGCCCGTGGTGTGGATAGGTCGCATCGCAGGCGTCAACCGGCCAAAGCTGGAAAGCACCGAGGTGCGGTGTCAGTCGCTCGACGCCGCGCTCGGGCAGCCGGGTTTGCGACTGGCGTGGACGCGTGGCTGCCCGTACACGCTCTACGACCGTAATTGCAGTGCAAATCCCGAGTCGTTCCGCGTACCCGCGTCGCTGACGACCGTCGCCGGCAATCTGGTTGCGGCTGGCGTGTTCGGCCAGTACCCGGACGGCTGGTTTGCCGGTGGCTTTCTGGGCTGGGACCTGGGCGAAGCAGGTTTGGAGCGGCGCGGCATCCGCAGTCATCGCGGCGAGTGGCTGACGCTGCTCGGCGCTGGCGACGGCCTGCGCGTCGGCCAGTCCGTCATCGCCTATCCCGGCTGCGGCCGGTCGATGGCGATCTGCCACAACAAGTTCAACAACGCCCCGAACTACGGAGGCGCTCCCGGCATACCGGGCAAGTCGCCGTTCGACGGCACCCCCCTTTTCTGATCCGCGGATACACGCATGAACATCTGGGTCCAGCTTGCGATCTGGGTCATCAGTTATTTCGTCTCGGCGGCCGCACGGCCGAAGCCACCGCAAGCCAAGCCGGCTGCGTTCGGCGATTTCCAGTTCCCGCAAAGCACCGAGGGCACCCCGCAGGCAGTGGTGTTCGGCGACGTGTGGACGCCGGATTGGATGGTCCTGGGCGTTGGCCAGTACCGCACCCAGCCGATCAAGCAAAAGGGCGGCAAGAAGTGATCGTGACCCTGGATCATCTACGCCGCGCGCCGGGCTTCGGAGTGCGGTCGGGATTCTGCGCGCAAGGCGGACGCGAGTGGTTCGCCTACTACGGCCTGGATTGGAGCGCGTTCGTGCGCGATGGGATCGAGGCCGAGGCCATTGAAGCCACCGGGGATGCCCTGGGCCTGCATCTGATCGCGTTCGCGCGCGCGGAGGCCGCGCGTGGGCAGCAGTAAGAAGCAGACGGTCGGCCACCGCTATCTGTTCGGTCTGCACATGGGCCTATCGCGTGGGCCGCTGGACGAGTTGGTCGAGATCCGCGTCGGTGACCGTGAAGCCTGGAAGGGATCGATCACCAAGACGGGTCGCATCTTCATCAACAAGCCCGACCTATTCGGCGGCGACAAGGGCGAAGGCGGCATCAAGGGCTGGCTCGACGTCCTGATGGGAGAAGCCGCTCAGGCGGTGCTGCCCGCGCTGGGCGCGCTGCATGGCGTGCCGACACCGGCCTTCCGCAACGTCACGACGCAATACTTCGATGGCCAGATCGCGGCGAATAGCCCGTACCCGAAGCCGTGGAAGATGCGCGTGCGTCGCGCTCTGGCCGGCTGGGACGGCGCTCCGTGGTATCCCGAGAAAGCCGTGATCTGGCTCGCCAATAGCGCCATCCGCGCCATGAACCCGGCGCACATCCTGGTCGAGTGCCTGACCAACCGGGATTGGGGGCGCGGTCTGGACCGTGGGGTGCTGGACGACGCCAGCTATCGGCGAGCGGCCGACACGTTGCACGCCGAAGGCTTCGGGCTGTGCCTGCGTTGGAACCGACAGTCGTCGATCGCCGACTTCATGCAGGTCGTCATCGATCACATCGGTGCAGCCCAGTACACGGATCGATCGACCGGCCGGCTGACGTTGAAGCTGCTGCGCGACGATTACCGGGTAGAAGACCTGCCGCTGTTCGACTACGAATCCGGCCTGCTCGCGATCGAGGAGGATGAAGGTGGCGCGCAAGACGGCGCGATCAATCAATTGATCGTGACGTGGTACGACCCGATCAAGGACGAAGAACGGCAGATCCGCGTCGAGGACCTGGCCGGCATTCAAGCGACCGGCGGCGTCGCGTCGAGCACCACGGATTATAAGGGCCTGCCGACTCCCGAACTGGCGGGTCGGGTCGGAACGCGCGACCTGACCATCGCGTGCTCCGGCTTGAAGCGATTGAAGCTGCGGTTTGACCGCCGCGGTGGCGTATTGGCGCCGGGCGGCGTGTTCCGCATTCGCGACCCGTTTCGTGGCCTGGACAACCTGGTCCTGCGGGTCGGCACGTTCGATGATGGCAAGCTGGCCGAGGGTGCGATCACCGTGGTCGCGGTGCAGGACGTGTTCGGATTGCCGGCGACGGCATACTTGGAGCCGCAACCCCCGGTTTGGACCCCGCCGGATCGAGTTCCGCAGCCGTCGCCGAACCGGCGGTTGATGGAGGCGAGCTATCGGGATCTCGCCACTACGCTGAATGCCGCGGCCCTAGCCGCGATCCCGGTTGATACCGGCGCCGTTCTGGCCGTCGCCGAACAGGCCACCGGCCTGGCGCTGAATTACGTACTGACCACCCGAGTCGGTAGCGGCGAATTCACCGAGGCCGGCGCCGGGGATTGGTGTCCGACCGCCGTGCTGGCGGATGCGATGGTCGCGACGACGGTGGCGGTGCAACTGTCGTCCGGGCGCGGGCTCGACCAGATCACGGCCGGCACTGCCGCATTGATTGAGGACGAGATCGTCCGCGTTGTCGCCGTCAACCCGCAGGCGCAGACCGCAACATTGGCGCGCGGCTGCGCAGACACGGTGCCGGTGCCGCACGCAGTTGGAGCGCGCATCTGGTTCTACGACGATTTCGCGGCGAACGATCCGACTGACTACAGCGTCGGCGAGACGGTGCAAGCCAAGTTGCTGACGCGCACGTCGAGCGCACAGCTGGACCCGGCGCTCGCGCCGGTGGACACGATCAAGCTAGCCCAGCGACAGGCGCGGCCGTATCCGCCCGGTGATCTGGAACTCAACGGGCTGCGCTATCCGGCGTCGATCGACGGTGACCTGGCCGTGTCCTGGGCGCATCGCGATCGTCGGCTGCAAGCGGATCAGTTGGTCGACCACGGACAAGGGTCGATCGGACCCGAGGCCGGGACGGCGTATGTCGTGCGGCTGCTGGATGCCATTGCAGGTCAGGCGCTCGACAGCCCGGCGACGCTTACCGGCGCCAACTACGCATCTCCACTGCGCGGCGCGTATCGCGTGCGCGCCGAGATCGGCTCGACGCGCGACGGCCTGACCAGCTGGCAAAAAGCCAGCCACACCTTCGATTTCAAGAACGGCCTATTGCGAACTGAAGTCGGCGACGACTTGGTGACCGAGGAAGGCGATTACATTTTGGCGGATTGACGATGGCGAACTTGAAACTCTCGCAACTGCCGGCGGCGACCGCGCTCACTGGCTCGGAAATCCTGCCGGTTGTGCAGGCGGGACAGACACGCAGCACTACCGTTGCAGCCATGGCCGACTTACGCAAGGGAGCGTGGCAGGTACCCAGTTTAAACGCGCCGTGGACCAACTATGGCGACGCATTCGCGAATACCGCTTACCGAAAGGACGGCAACCGTGTGCAGTTACGAGGGTTGGTGAAAGCGGGAGCAGGCGGCAGTATGATCTTCACGTTGCCCGCTGGATTTCGTCCGCCTGCGCAGCAAATATACGTCGCAAGCTGCGACGCCACGACCCCGGCTCGCGTTGATGTCAGGAGCAACGGCGACGTGGTTATCGCGCAGCCCGCCACTGGGACGTTGGGATGGTTGTCACTCGACGGCATCGCATTCTTCGCCGACTAAGGACGCATCTAAAATGGCTGCGGCAGGAAGAATAGATCGCAGACAACCCTGTCGCTTCGCTGGACCGCCTACAACTCGTCGCATGGCCGAAAATTCGTTCGTAAAAGGCCCCCCCGCGCGTAAAAACGCTTCCTTGCTGCTACTTGACGAGCTCGGGCGGTGATTCCGCGCTCAATATGATCGTGGTTTTATTGCAAGCACCGAGATTGATAGTGTTTTCTTCTGGTCGCTGGATAAAATTTCCCTCCAGTTCGACATAGCGCCTGTCGTAAAGTGACGTGTCCATTACCTCAGGAATCAACAAGCTGATGCAGTCGTCAGCATAGTTGCCGCGGTCAAAAGCGGCTCTACTCTCCCACAGGCCATAGCGTTCAAAACTAGAGGTCATCCATCCGAACACCTTGACACGCTGTCCGTGATGCTCAGACATCATGGCATTGAGCATAGATGGGGTCAGAGCATCACTAGACTTAGTTGGGATTGCGCTACAAGACGTAAGCACCAAAGCTACTAAGGTCACGTTGATAGATTTCATTCGCCCCCTCATCAGCCGCCGCAGTGATCGTGATGATAATCATGTGCCGCGCGGGTGATACCGCAAGAAAAAGGCCTCGTTCTCGAGGCCCTCTCCTTTTAACTCAAAAGCGGTCAACGATTTCTAGCGAATCAATCAATTGAAGAGGAAATCGCTATTCTTGACGATGGAGTCAACGCCAGCGTCGTTGTAATAACATTTATCCTCGAACTCGATAGTTCGTCCAGAGTGGCCGTATAAAATATACGTCTCTTTTCCGATTTCTATGAGGGCATTCTGCTGCCCGGAGAGACACTTGGACGAAGTAGACTGCTTTAGGTGGTTTATAACGGCCTTCATGAAGCCGGCGCAATTGCCGCCACATTTGCGATAAATTTTGATAGAGGCATCGCTCTTAATTTTGTTCCTATCCAAGGAGTAATCGCCGGTCCTGGACACGAAATAGAAAGATACAGAGCTAACGCCCCTCAATTTCTCGGATAGGTGGGCGGACGCAGTTTGTGATCCGGTGTCGGCTATTGCTGATGATGCAGCACACCCCGCCATAGCCAAGATAGCTGAAGTAAAGATCCTCAACATTGTTTTGTACTCGTAGGGCCACAGGTGACTACTGTTCCTTTGGAGTCACTGTAACTCTTTCTCGGCGCCTCTCCAAGCTCCTTCGCAACTTTCCCCTCGACAGCTGCAGCGCGATTTTCTTCAGGACTGGACTTGAATGACACAGAGAATCCGCCGTTAGCCGTGTCCTCCATCTTTGTGACAGGAGCCTCTAGGTTAATTCTCATTGACTCAGTACTGGTGCGATCGTGCTGTGCTGCATGGCTGATTTCGTGGGATGCGCCGATCGCTGGAGACTGGACCTCTCCAGAAGATTTAATGCGCAGGCCACTTATTGGATTTATGTTCACCGTTCGCGTGTCGCGGTCATAGCTAAATGGCGCGTCGGCACTGCGGTCAAAAGACAGCGTGTACAGTTCTTTGGAGTTTTGTATACGGACTATTTCATTGGTTGCGGTGGGTGAGAAGGCGAGATATGCCATCGTCGCTATTCCATCAACAACGGTGGCGCCATTTTTGAAAGCAAAAGTAATTTCGCGACCATCTGGGTCCTTAAATTTATAAGGATTGTTACTCGCATACCAATAACGATTGAAGTTGGCGCCGGTGCTCCCGTCCGCAGTAACGGGATCAATACTGAGAAATATGCCAAGCGTCTGATCGTAGTAGCGTTGCTGCATGTAGGCCAGACCAGTTGTCCCATCTACTAGGTGCCCGGTATAGCCAACTCCATCGTAGGCTGGTTTTCCGATGGCCGCACCGTAGGGCTCCCAATCCGTGCGATCAATTACCTGACCTGCTTCATTGGTCGTCGCTACCGGGCTACCCAGCGCATCTGTGTGCTGATACTTGATGCGTGTCGTGTCGCCTGTGTCAGTGGGCACGCGCTCAAGCTGGGCGATCAAGCTGCCTCCCAGATAGACATACGTATTTTGGATGTAGGAATCGGGGAAATCGCGCCGCAACAATTGCCCTGACGCATAGAAGGACTGTTCCGCTGTCGATCCGTTGCGGGTCACGGATATCCGCAGTCCCGCAGCGTCGTAGGCGTAAGCATCCAAACCAACGACCTCCCGGAGCCGATTGCCATAGTCGAACTTGAACTGCCGCCCGTTCTTATTGGTTAGATTGCCTTGCGGGTCGTAACTCAGCCCAACGATGCTTGCGCCCTGCGCGTTCTGGACGTTGGTCAGCTGATTGCGTGTGTCGTAGTAGTAACGGTGATCCTTCACCCCTCCCAAAGACCAACTCTTAAGGTTGTCCAGGGCGTCATAGCTGAAGCGATGCCAGCAATCTCCGCCGAAGCTGCATGACCCCACGGTTTGCAGGTGATCGAGATCGTCGTACTGCATTGAGCGGTTGTAATGATCGCCACGGGCGCGATCGTAGATTTGGACGACGTTGCCGTTCGGATCGAATGCGGATTCCAGATCGATGATGCCGGCATCGGTGCTGCGTGCCGGTAGCTGACGGGCGTTCTGCGCCATCGTATGGACGATGCCGTTGCCATACGTGAACGACTTCAACGCACCGTTGGGGTAGTAGCTGATCGCAGAGGCGTACGTCTGACCAGCGTTGTCGCGAACCATCGTCGGCTGGCCGAGGGCATTAGGGGCATAGTCGAAAGCGCGTGTGGAATAGTTGGCTTCACGGACGTTGCCGTGACGGTCATGTTGATAGGTGATGTCACCGCTATAGTTGCTTTCGCCGGTGGGTAATCGACGCTTGTTGTAGCCATAGGAGTTGATGACCGTGGTGGGGGCGACTAGGTTCGTCGTGTAGACACTCTCGGGAAGGCCATCGGGATGGTAAAGCCATGTTTGATTCCCCGCTCCGCCCGGGAACTTAAGTTGGTATAGCTTGTTGTTCTGATGGTAGCTGCGGGTCACTTTTCTTCCGGATACTTGAGTATCTGTCCGGTTGCAGGTCGTGGCATTCGGAAGGGTCAAGCCCGCCGCCGACCAAGCTAGATTGCCGGCTCCGTCGTACTCCATCACAGTCGCACCGATCTCCGGCTCGATCGTCTTGCACAGTTGCTGATACTGGTCGTATACGAAGCGTCGCGACAGCATCTGCCAACCTGGGATGGAATGAAGACCCGATTGACCGATCAGTTCGCTAGCGCCGGCCGCCACGCCGTACGCGTAGAGCTTCTTGTTTGGATGGGCACGGCGAATCGCTTCTGTCAACGGGAACGTGAATCGATAGGCGTTGGCACTCGTTCGGCAAGCCGTCGATAGAGCCGGTTCGCCGGATTGATTGGCTTGAGCCGTGCCGATCAGCATGCCGCCGTTGGGCGCGGGGTCGCGGGCAAAGAACTGCACTTCGATGGAAGCGGCATTCCCGGCTAGACAGGCCCAGCCGTAGGCATCGAATCCACCCGCGCCGTTATCCCGAACGCCCTCTATCTGGCCCAGGATGCTCAACGCGCCCACCGTAACCGTGCGGGCCTGCGATGTACCGGTCTGGCTGTTGTTATCGGTGGCCTTGGCCGTCACCGTGTACTGCCCGGCGGCGACACCGATCCAGCTAAGTCCGAACGGCGTCTGAGTGCTAGTACCGATGGATTGCCCATTGGCGAAGTACTCCACCGATACCACTTGGCCGTCGCTGTCGGCCGCGGTGACCGACAACGGGATAGTGGCGGGGGCACTGTAGGGACCTTGCGGAATCTGGTGCAAGTCCACTGAGGGCTTAAAATCGCCAGGAATTAGCACATCGAACGAGCTATAGGCCTCGTTGAGGGTGTTCCCCTGGGCATCGGTCGAAACAGTCCGAAGGTTGTAGTGTCCGCGCCCAAGGCTGAGGGCATGATCCGGAACCGTGCAACCCGAGGTTCGCAGCAGCGCATCATCGAGATACAACTTTACGGTCTTCGGAAAGAAATCGTCGTCGCTGACGCACTGTATCTGAACGTTGATCGCGGCCGGAGCGTAATAGGGGCCAGCGGGCGACAATAGAATTAGAGCCTCACCCGCAGTGGCGTTAAAGGCGGATGGCAGAACAAGCGCTAGTGCCAACAGCGCCTTGTTAAATATCGAGTGCGACATAGACTATTGGCCTCGCATACTAGATGGCGCTGGGCGCCGTTCAATTCCGTGTACTCGTGCGGGCCTTCAGGGTGCTCCGCTGCGCCTTATTTCCAATGGCTTGCCGAATACGTCGCGGCGGATGTACGTGGCCGCGTCGGTAGGCAGATTTTGTTCGATCGGTAGCGAGTACGACGGCGCGTCGAAAGCCTGATAGCGGGTGACCACGGACTTGCCGCGAGGGTTGGTCACCTTCTGCTGCATGCCCGGCAGATATTCGGTGACCGTGCGCAGCACCCCTAGCTCGGAATCCTGGCGGACCTCGGTGGCGCGGCCAAGCGCGTCATAGGAGGTAGAGGTGCCCGACATCGCCGAATCGAAATTGACCACACCGTCCACGAACGGATTGCGCGGGTACGAAGCGAAGACCACCCGGCCATCATGGTCGTAGCGCTTGGCACTCCAGCGCGTGGTCGCCTGAGGGTTGCTGGTATCCTCTTCCTGCTCGGCGACCGGCCGCCACAAGGCATCGAAGTATGTCGTCTTCTTTCGGTTGCCGGTGGTGACGGTCTGGCGCCAATGACCGGCCGTCAAGCCCACTTCGGTCGCAGCGACGGGTTCGAAGCGTAGTACCGTGTCGTACCATGCGACGGTATCTCCGGTTGGATAGACGATCTTGACCAAGCGGCCCGCTGCGTCGTAGTCGTAAGTCTTGGCGTATCCGTTCTCATCCGTCACGGAGCGAATCCAGCCGTTGTCGTCCACGACGGCGGATGTAGCAGTGCCATCGGCATACGTCACCGACTGTGGCAGCCCGCGCTTCCAGTTCGAGAACGTGGTGACGTTGGTGTTGCCATCGGCCGCGGTCGCGATGGTGCCGTCGGCGTTGTAGCTCACGGTTTGCTGCAATTTGCCGAAGGCATAACCCTTGATCGGCAGGTCCGTGGTGGCATGGAACTCGGTGCGATCGGTCTCGATGCCGTTGGTGGTGGAGCGCTGAACCTGACCCAGCACCCAGCGGGTCATGCCATCGCGGTACTCGGTGGTGTCGTTCTTGCTGAAGCCTAGTGTATTCGACTTGATTACTTTGGTCGGGCGGGCGAATTGGTCGAAGCACAAGCCAGTCGTGCCGGTGCAACTGCCGTCGACCTGCCAGGTGAACGTCGCGCCATCCTGGACGATGATCTTTTTCTTTAATGGTCTGACCATCGACGAGGTCGAATCGTCGCCGCCAAGCAGTTCGCCGTAGAACCATGGGAACGGCATAGTCGTACCGTTCGAGTACTGCACGTACTCGCTGGACTCGGAGCGCAGCACTTTGTTATCGGCGCTGACGGTGCGGGTGCCCAGCGGCTGGCCGTCGTTGTACTCGTAGATGTAACCGAAGTCATGCAAAGTCAGGCTGCCGTCGGGGTTACGCACGGTAACGGTCTTGGCCACCGAACAACCTGGGCAGATTTGCAGCGGTCCGTCGATGCGGCCTATGCCCATGTCGCCATAGTCATAAGTCCATTCGTGTGCGATCCCACCGGTGCCTGTGACCGTCTTACGCGCCAAGGCGTAAACATCGAAATAATCGGAAATCAGTAGCTCGTGCGGGCCATCAGGATTGCCGTTCGTGTTCTCAAGAGCTGGCACACAGGCACTGGCCGGTGTTCCGAACCGATGCAGGCGGGTATAGGGCATTACGAAAGTTCCGACCGCACCGGAAGGATGGGCAGCGGTCAGCGTAAATGTCTCCGGACCGAAATCAGGCTCAGCGCAGGAGCCACCGTCAACATCGAGCGGGGTGTAGTTCGGATTCAGTCCGCCATATTGCATCGGCATGTTGTAGCTGTAGGTCCAGGCCGACTGATCCGGCAGGGTCACGCTGGCAAGCAGGGGAAACCGGTTGATGCCCAGGGCGCCACCACCGCCGGTGTAACCGTATTGCCATACCCGGCCGTTGGCGCGGGCGCGCTGCACCGTTGCGCCGCCGTCGTACTCCAGGTCGATCCGCCGTCCGTCGTCGGCGACGACACTGAGCAATTGCCCGCCCTGCGATCCGCCATAGTTGTAGTTGACGCCGTTGCCGAAACGATCCTCGACCCGCGTTGCCATGAGATAGACCCTTATGCGGCCGAATCCCGGCCGGGTCGGGGTACCTTTCATAGCACCGGCGCCGCGGTAGGCCATGGTGTTGAAGAAATACTTGGTGCCGCTGGTGTCCACTCCAACAAAGGCTTCACCGGGGTAGTTGTTGACGCCGTTGGCGACGCAACGAAAGCGCATGCCGTCACGGGTGGAACGCGTGTAGGTCTGCCCATCGTTGGGCACGGCATTGCCGGTAGTGCCGAGGACCAGCATTTCCTGATCGCCGCCGCCGGGCAGGTGGACGAAGTTCCCTTGCCAGATATCGCGCAGGCGATGGTTGAAAGGAATCTTGGGCAGCCAGTTGTTCGAGCAACGGTTGTCGGTTGGCCGGCTGCCTTCGTTCCACTGCGTGTTGGCCGGGAATGTTCCGTAGACGTAGGGCACGTCAATGTCCCAGGCGCCGAAGCCGCCCAGGTTGACCACTTCTTTCTTGGCCTCGACCTTGAAGCGCCGGCTCAACCGCACCGGCAGGGACGAGTTGCCGGGAATATCGATATCGGTGACAGCGAATTCGGTAGACCCGTTGTAGAGCGACACACTATCGCCGAACAATCCCGAGCTCAGCGCTGTGACCATCTCTGTCGCGCGGATGCGCTTCTCGTACTCCACCGGAGGCATCAGGGGGGATTGCGCCAAAGCAGAAGCGCAGGCACACAGTAGAGCCAGAGTGCTCAGGCTGAGCACTTTCGACATATGCATATTCAGATTTCCCCCTTTAAATTTAAACGAGTCGTACCGTGCCACGATTTCGCCAGAGCCCGATCCGTCGCCGTGTCGAGACCCAGCGGTGCAACCAAATATCGCCCTTGTCTATCGGCCGTTATCACTAAATAAATGACTGTTCCAGGAAGCCGCCGCATGCTTCCGAGACATGATGGCCACTATAGCCAGTATCTAACGCAAGCGTCTCTTTAGCTTCGACCATCCCGCCAGATGGCTTACTAGAAAGCTGTTTTGCACCGGTGAACTTGTCCTCGCAGATGACATTAGTGCAGATCGTTGGGAAAGAATGTAGGAAAATTCTGATTTGCTTTAGACATCTGTCCACGTTAACGCAGACGACCGTTTGTTTGGAGTAGACAGCGGTCCACGATCATGTGGACATAAAGCATTTTCGAAATGATCTGGTTGCTAACGGCGAAGCTATTTTGGCTTAGTCACGTCCCACGGACGCACTGGCCAAGAGGGATAATGATCAGAATATTTGTTGTTGACGATCATCCGCTGCTACGAATCGGGTTGCGTTGGTTGTTGGAAGCGCAGGGCGATATTCAAGTAATTGGGGAAGCGGGAAGCGTCGCGGACGCGATGATCATGATTCCAGCGGCGGGGCCAGACTTGGTCCTGTGCGATTTCCATCTTCCAGACGGCGATGGCCTGGATGTGGCGCAGCGACTGCTCCAAGAACGTCCCAATCTGCGAATTCTCGTCGTATCGGTTCTGGAGGGCGGCCCCATTCCTCGGAGGCTGCTAGCTGCCGGCGCATTGGGCTATGTGTCCAAAGCCAGGGACGGAGCAACCTTGCTGCGGGCGGTGCGAGAGGTAGCGGCCGGACACAGATTTTTGGATGAGGCATTAGCCGCCAGCATTCTCTTCGAGCCTTCGCCATTTGATCGGCTCAGTCCACGTGAACTGGAAGTCGCCCGAATGATGGTCCGGGGCGAGAAGACCCCCGCGATTGCGGAGGCGCTGGGCATCACCGAGTCGACAATTCGTACCTTTCGAGCGCGAGTTCTGGCTAAGCTCGACGTGCACAGCGAAATTTCCCTAATCAGACTTGCGATGGACTGCGGATTTGAGAAGTAGCGAGCGCGATGACTTAAACTCAAAATAACTTATGAAACGAAATCATACGATCCCTCTCTGGCAAGAATGAGTGCTTTGACTCACCGTTGCGTAGACTGTTAAATCAACGCAGCTACTGGGTCAGTTCGAAGGGGGCAGCCGCTTGAAAGTCGGCGAATTTGCGGCGATGCGCTCGCCTAGCCGCCGCAACTCGACCCGAATTTCTTCGGGCGCCTGATCGACCAGCGCATCCCACTGTTCGCTGAAGCGCAACGCACGCTCAGCGGACGTGATATGCCAGGAGTCCGCGACTTCCAGTTCGTCACGTAGCGCTGAAGCGCGGGCCTTGGCTTGGCGGGTCTTAATAGGCATGGGCGTAGTCCTGATTGCTCCGCCCGACTCTACTCCTGCCCGTTGCCTCTCATGGGATCGCCTGGACATGGCGTGGACCAGCGATCGGCGCAGGATGTAGGCGCACAAGGCGCCAGCCTGGGCGCAGCCAACCGACAGAGTCTGGTACTGACTTGAGGGGAGCCTCACAACGGAAGGTGCCTCGTACGCGGATGCGTATGGCACAGGTAGCTTGAGAGCCTGGCCGGAAGTAACCCGGCACTCCGCGCGGTTGGGGCCGCTAGTCTCTTCCTCCGCGTGGGTAACTTCGTACAGCCGGTCACTGCTGTCGCATAGGAACTCGTGCTCGGCGCCGGAAATTCTGGTGCTGCTGCCTATGATGTCGTTTCGCTCACCGGCAATCACGGTGGCTCTCGTTCTATTTGAGCGCCCCCGCAACAACGGATCTTTCTGGGACCGCTAGCTTATGCCGCGAAACCCGCTCGCCGCCGCTTGTGCGGCGTCACGACCGCGCAAGACTTGGCGTTCAAGCGGCAGCCTTCATCGAAGCCGAGGAAGTGGTCTGGAGCCCACAATGAAAAATACCGCCAAGCAAGAGTGCAAGACGTTATCGGAACAGAACTGGTCGTTGAGTACGTTCACGGAGTTCTACGAGCGCGTCCTGGGGCCACGGCTGTTCAAGCCATACGGGGAACTTCTGGCCCACGAGATCTGCAAGGACATCGATCCGGACGCCCCACCCTCGAGCATTCTGGAGGTCGCTTGCGGAACCGGCCGCATTACCGCCGCTCTTTACCAAGACCTGGCCAAGCCGCTGGGCTTGCAGCTGGTCGCCACGGATCTGTCGAAGATCGCCATCGAGATGGCTAAGAATGTGCTCGGCGAGGAGCTGCAACGCGACGTTGCGTTCCACTCAGATGTGGATATGGCGGATCTTCCGTTCGCGGACAACAGTTTCGATGTCGTCGTCTGCGGCTTCGGATTGATGTTTCCGCCGGACAAGGCCCGGGTCGCTCGCGAGTTCAAGCGCGTGCTGCGTCCGGGAGGAAAGATCTACGGCACCGTCTTCCAGTATAACGAGTTGTTCGACTTGGCCCTGAAGCAATCGCAGAAACACTTCGGGGCTCCATCCGCCATCATGGGCGCGGCCCTAAGCCTGACCGACCCGTCGGCCATCACGCGCGCCTTCTCCCTCGAAGGCCTCAGTCCGGGCATCGGCGAGGTGGCGACCTCGCGTGCCCTGTCTTTCTTCCTGGACGACCTCGACACTCGCGAATTCCTCTTCAACGCCTGCATCCTGCTCGAGGAGTTCAACCAGTGCGACGCGCCTACCCGCGAGGCCTACCTGGACGCGATGCTCCAGGAATTCCACGCGCAAATCCCCAGTCGCAACTACCAAGTCAAGGCTTGGCTCCTGCGCGGCGAGGTCGGCCAGGCTTGCAAGGAATCGGTCGTCCCGAGCCCGCCGCCCAATTTTTCCGAACTGAGCGACTTTTGCCGAATCCCGCCGGCGCCCATCGGGAGCGACGCGGACAGCCCGTTCTCGCCACAGGCCGAACGTTCGCTGCGGCCTTATCGCACGATGAAGCGGGTCTTCCTGGCCGAGCATCCGGACTACCCGGAAGCCGATGTCGAAGCACTGCGCAAGAGCGAGTTCTCCCGACTGGACGCCCTGCAGACGACCTATCTGGACCACGTGGGGGGCACGATCGCTCCGGACAGCCTGATCGAACAGGATTATCGGGTGCTCAAGAACAGCATTCTCGGCAATCCGCACACCGGCTCGAAGTCCTCCGATGGGGCACATGAGAAGGCGCGCGCGGAAATCTACCGGTTCTTCCGCTGCTCGCAGGACGAGTACGAAATCATTTTCACGCCCAACGCCAGCGGAGCAATCCGGCTCATCGCGGAGTCCTTCCCGTTCGAAAGCGGCTCGCAGGTCCTGCTCACCAAGGACAACCACACTTCGGTTCATGGCCTGCGGGAATACGCGAGAGCCAAGGGCGCGTCGGTGAAGTACATTCCACTGGACAACGAACTTCGGATTATCGAGAGCTCGATGCAGCGTTCGCTCGATGGGCTCGTCTCGGGTCGCCTGCACCTGTTGGCCTATCCCGCGCAGTCAAACGCCACGGGCGCTCGGCACGACTTGAAGTGGATCGGGCTCGCGCAGGAACGCGGCGCGATGGTGCTGTGCGATGCGGCCGCGTTCGTTCCGCAATCCAGGCTGGACTGCTCGGTGCACCGGCCGGACTTCGTGGCGATCTCTTTCTACAAGATCTTCGGCCACCCGACCGGGACCGGATGCCTCATCGCCCGCAGGTCGGCACTGCGCGAGCTGACCCCGCCGTCTTTCTCGGGGGGCTCGGTGTGCTACTACTCGGGGCCTTGGTCTCCGACCGACCGGCTGCTGCATCGCGAAGACGGCAAGCGGTTCGAGATCGGTACGCCGAACTATGCGTCCTTCGACGCCATCGCCCTAGGGTTCCAGTTCGTTTCCCGGCTTGGGCTTGAGCGCATAAGTGCGCGCTCGTCGGCGTTGGCGAGGTGGCTCGAAGCGCGGCTCCAGGAATTGCGACACGACATCAAGAGCCAAACTCCGCTTTGTCGCGTCTACGGCCCTTCGGCGGAGCACAAGGGCGCTACGGTCATGCTGAACTTCTTCGATTGTTACAACGCCGTATTCCCGCATGCACTGGTCAAGCGGACCGCCGAGTCCTTCGGCATCGTCGTGCGCAACGGATGCTTCTGCAACTTGGGCGCGGTGCAGCAAGCCACCTACACCACGGCAGGCGCGGAGCATTGCGAACTCGACAAAACGGAAAAGATCCTCGACTGCAAGGCGTTCGACGACAACATCCTCAACAAGGGCAATTGCGGCGCCATCCGGGTCTCGTTCGGCCTGGGCTCGAACTTCCGCGACGCGTACTGCTTCTACCTATTTGCGAAGTGTTTGCTAAATACCGAGTGCGCACGGCTGGAGGATGCCCTGGCCGGATCTTCGGTGAACTGAGATGGCACGACTGGCTGCAGCGCTCGTATCGGCGATGGCTTAGCCGGGTTTTCCACATTCGGGGTTCGGGTGCGTTCAGCGCTGCCACCGCCATTCCAACTGTCCAGGCAAGAAGCCCAAGCCCCCACGGGAAGGTGGATGTTTGGGGCCGATCTCGATCGATAGCCACTGCTCAGCCCGGACATCTGGGCTGTACGCATCATCCCAGGGCCCCGCATGGTCTCGGACAGAAAAATTTATATGTCGTCCGTCAAGTACGGACCTGGATGCGCAGTGTCGTGGTCAGGCCTGGTGACTGTTGGCCATAGGACGCGCCGAGCGCCGTTGTCCCAGTAAAACATGAGGGAACCATCATGGCTGGCAAACCGCGCTTCGAAGTGTATCGGGAAGGCAGGAGGGCGGGCGGGCAGCGCTCATTGTCTAATGATTTCTTGGCCGGATCTGCGACTGATGGGCAGTGGCGCTGGCGACTGGTCGGCGGGAACGGAGAGCCCATGGCCCATGGCGAGTCCTATCCCGACAAGGGCTCGATGTTGCGGACCATCGACATCATTGCAAACCTGGATGGCGCTGAGATACGGGAAGTCGACGGCTAAAGAGCTACCTGCCTATGTTCGATCCGCCTGGCCGGTCAGTCTAAGGACAGCACGCTTTATGGGTATTCATGTCAGCTATCACCCGTTTTCGCCAGCCGAAATACACTGCCTGTACTTCGACATAGGGCGCGGTGCGTGCATTGAGCGCTTAGTCTTGCAGCTCGGGCTGGATCCGGCTGCTTCGGCCACGTTGAAAACACTGCTGTCACATGGCGGCCGCGCTCGTCCCGATGGGATGAGTCTGAGCGAAGCTCACGCCTACAACATGGACAGAGTTTCGGGCCTGCTGCGGGACTGCTGGTATACGAGCAACTGTCGCTTTTCCGCGCTATTGGAGCATCCAGGTTTTTGCCAATACGTGACCGATTGGCGGAATCTCATGGCCGAGGATGTCGTCCACGAGCGTTGTGCTCATGAGAAGGACCTGCTCCGAGACGACGGCATCTTCTTCCTGAGTTGCGGAGCACTGAAGCAGCTGCGAGCCGAGCATGCTGAACACGGAGCGGTGCGCTCGCAGTTGGCTCGCGTGTTCCCACGCGGCTGGCTGCCGATCTTCTGGACGGCGGCGGACCACGCCGTTGCACGCGAGTGTGGGCTGATCGAAGTGGTAAACCTAGTGCATCCTGACGTAATTACTCCGTCGCCGTTAATGGCGTAGTTGTCGGCCGGGCTTGGCTTGGTGAACCTTAGTCGGTCTATGGAATAACGGCTCAGTCGCACACGGCCGCGCGCGAGTTAGAAAGAGTGAGCGTCCGACGTTATGAGGATTTGTGCACAGAAGTGACCCGCAGGCTATCTGATAGCGTTGCCTTACATGCCGCATCCACAACGCGAACTGGCAGTGAAGGAATGAAGGGGGATTGAAGACAGTCGGCAGCTGCTGCGAGCGGCTCGAATGCTCGCACTATTTTTCGAAGCTGAAGAGACTCTCGCACCGCGGCCGCGCCCGTCGGGCATGGAGTTCGTATACCAAATTTACGAGCACGCCCGGACCGCGTTCATGCCGCTTGATCAGACGCCCTGAAGGACGGACTCGATGGCGCCGTAGCGCAGGCGGTCCGTTTGCCAATCATATGGTTGGTACAAAGCCGGCGGTTCAATCGCTGAGCCGCCCTCACAAGGACTGCAACACGCTAAGCAAGTTTGTGGCGACCGCGTGATGCATCAGGAGACTCAGCAATGATAGGGACATTGCTCGACTTTGCATCTGATATGGCCCGGTGGCTGCATGTCCTCGCTGCGTTCGCATGGCTGGGCGGCGGCATGTGGGTAAGACGCCTGACGCTGCGGGCGAAGCCACTCCTGGATCAGCGGGCCGAACTGGAGGTCTGGGACACGCACAGCCTGTCGTTCTGGCGGAGCTCGAAAGTCTCGGCACCCACCGCGGCGGAGTTGGACGGGCTAGTGTGGTCGTTCAATCAGATTCGCTGGCTGATCGGTACCGGCGTCGTACTGTTCGGCCTGATCTACTACCGCCAACCTCTGGCGTACTTGATCGACCCAAGCATCGCGCGACTGTCTGCCCGCGATGCGATCGAAATCTCGGCCCTTGGCCTGATAGGCGCGCCCCTCCTCAACGAGCTCGTCAACCGCATACCACTGCGTCACAAAACCTTATACATGGCCGCAACCATCGCTCACCTCCTCGGCTGGGTGTGGCTGTACGCGAATCTGTTCTCCCAGCACGGCGCCATGATTCAGATCGGCGCCATGCTGGGCGTAGTGATCGCGTCCAACGTCATCTGGTGGCTTTATCCGAGGATGCGCAAGGCCTATGACGCGGTGCTGAAAGGCGATCAGCCGGACCCCATCGACCGGCTGCTCTGGGATCGACGGGGCTTGCACGCCCATATCACTTTCGCCGTAGTCTTCCTGATGCTTTCCAGTCACATGGGAAGTCTGGTCCGCGCTAACGGCCACCCGTTCCTGACCATTTCCACCGTACTGGCTCTGAGCGTGGGGGCTCGATGGGTTTTCGATGTCACCCACCGGAATGGCGGGGTTATGCCGATCAAGCAGCGCTGGATGTCCGTGGCTGCTGTCTTGGTAGTCGGGCTGGGAATGACCTGGATGGCCTTGCCGGAGCTTCCAACCGAACAGGTCGTCGCTCACGCTAATGCACCTGCTCCGGCCAGCATTGCCGCGCAGCCGGTTAAGCACTCAAGCCCGAGTTCAATCGCGAGCTCGATCGTCAGTGGAACAATCCCATTGCGTGCCGATGCGATCGTTCAACGTCGTTGTGCGGTTTGCCATGCCGCGCAACCTTCCTTCCCTGGCATAGCCTCACCTCCGAAGGGAATCGTTTTCACATCTGAAACCCTGCCTCTGTATGCGCGGCTGATCGCCACTGTCGTGCAGAGCGAACGCATGCCGCCAGGCAACGCCACGGACATGCTGCCCGAAGAGCGCAAGGCAGTGACCCAATGGGCGACCGAGCATGCACACTGAGCTGCTCCCGTATTGGTATCCGATAGCGCGCAGCGAGGACGTGCACGATCGTCCCGTTCGCGCGTCGTTGTTGGAAAACGACCTCGTGCTGTATCGAGCCGGCCAGCAGATCGTGGTAGCTGTCGATCGTTGCCCGCACCGCGGCACGCGGCTCAGTCTGGGACAGCATCGAGACGGGGCGTTGATATGCCCCTACCACGGTTTGGCCTTCGGACTGGAGGGGCGTTGCACGCATATACCGGCGCATCCACACCTGACGCCATCGCGGCAGTTCCAGTTGTCTACTTATCCCGCGGTGGAGCGTTGCGGGCTGGTCTGGACCTGTCTTGGAACTACACCACCGCCGTTTCCGGAACTGAGCTCCGATTGGGATGACCCTGCATTTCGTCAGGTAGCACCGGATCCGGTGCCGATCGCCGCCAGTGCGGGCCGGCAAGTGGAGGGCTTCATCGACGTGGCGCATTTCGCGCACGTGCACACGACGACCTTTGCCGATCCCACCAACGCGGCCGTGCCTGCGTATTCGGTCCAGGTCGGCGAAGGTCGGTTGCGTTTCGATTACTGCAGCACGGTCTCGAATTATGCGGTCGGCAGCGGAATGACTGCGGACGACTTCGTCTGGCGTCGCAGCTTCGACGTCCGCCTTCCCTATCTGGCTCATCTGACGGTGTACTTCCCCAACGGGCGCCTGAACATATTGAACGGCGCCAGCCCAGTGGCGAGCGACCGCACCATGCTGTTCTCTCCGGTGTGTTTCGACCTGGAGCTCGGCACGGACGAGGCAGTCAAGGATTTCAACGCCCGCATCTTCGCGGAAGACCGCCTGATGGTGGAGAACCAGCAGCCACGCCATCTTCCACTGGAGTCCGGCGAAGCGTCCTTCGCGGCGGATCTTGCATCCGTTTACTACCGGCGCCTGTTAAGGGAAATGGGGCTAGCCACCGCATGAGCCGCCTTCTTAATCCCAGCGAAACCCCACCGAGCTCTCGACGCCGAACGAAGTGGGACGACAACGGCGCAGCGAGCTGGAACGCCTACCGGATCATGCGAAAGAGATCATGATGATGGACGCCTTGATCGATTTCATGACCGACATCGTGCGTTGGCTGCATGTGGTCGCCGCGATCGCTTGGCTGGGCTTCGTGCTGTGGCTGCGCAGACTGGCGATCAGGGCCCGCTCAGTGCTCGACTCGTCGGCCGATCTAGAGGTTTGGGACACCCATAGCCTCGGGTTCTGGCAAACCGAAAGGATCACTCGACCGAAGGCCTCCGATCTGGAAGGGCTAGTCTTGTCGTTCAATCTGATTCGTTGGTTGTTCGGCACCGGCCTGTTACTTTTCAGCCTGATCTATTACCGGCAACCCCAGGTCTACCTGCTGCTCGATCCCTCCGACGCGTCGCTGTCGTCTCACGCGGCAATCGCCCTGTCGCTGGCCGGACTGATAGGCGCTCCGCTGATTAATGAGACGATCAACCGTATCCCGTTGCATCGCACGATCCTCTATTACGTTGCCTGCGCCTTGCATGTTCTGGCCTGGATGTCGTTCTATGCGGACCGGTACTCGCAGCACGGCGCGATGATCCAGATCGGCGCGATGCTCGGAACGACCGTATCAGTCAACATACTTGGCAATCTCTATCCAGCCACGCGTGCAGCGATGGTCGCGGTGATGCGCGGCGAGCAGCCCGATCCGATCAGGAAGCAATACTGGGATCGACGCAACCAGCACTCGTTTCTCCTGCCTGCGATCGTCTTTCTGATGCTTTCCAGCCACATGGGCAGCGCCATCAAGGCTAATGGCCATGCGTTCGCCACCATCGTGATCGTGCTGGCTCTCAGCGTGGCCTCGCGCCATGTAATCGAAATGGTCCACCGCAACCACGGCATCGTGCCAACGCGATTGCGCTGGGCCGGCGTCGCTGCCGCGCTCGCTCTGGTATTGGCATTGGCGTGGTTGGTGGTCATCGAACACCAAGTCAATCTTCCGGCCACGGCAGACGCAACTGAATCGCCCAGGCTTCTGTAGACAGTCGTCAGCCGTTTAGTGCGTACCGCCTTTCAAACTCTATCGGGGACAGGCCGTCATTGGAACTGTGCCGCCGCTTAGGGTTGTAGAACAGCTCGATGTAATCGAACACATCGCCTCGGGCGTCGGCATGGGTGTTGTAGATCCGCTGCTTGATCCGCTCGCGCTTGAGCAATTGGAAGAAGCTTTCCATTGCGGCGTTGTCGTGACAATTCCCGCGCCGACTCATGCTGCACACGATGCCATGCGCTTTCAAAAAGCTCTGCCAGTCTTCGCTCGTGAATTGACTGCCCTGATCCGAGTGCAAGAGTAGTCCGGGTTCGGGCTTGCGGCGCCACACCGCCGCTAACAGGGCTTGCAGCACCAGATCGGTGTGCTGCGTCGGACGCGTGGCCCAGCCCACGACCTGGCGGGAGAACAAATCCAACACGACGGCTAAGTACAGAAAGCCTTCGTAGGTTCGAATGTAGGTGATGTCGGTTACCCAAGTTCGATTGGGCTCTGCCGCAGTGAATGCACGCGCCAACACGTTGTTTGCCACCGCGCCGATCGGTCCGTTCAAAGGCCGCGGACGCCGGCCATAGCCCACCATGGCGCGCAGCCCTTCTTGCTTCATCAAACGCGCAACGCGGTGTTTGCTGCACGTTTCACCCAGTTCGCGAAGATCCTTGGTGATCTTGCGATGACCGTAAATCGATCCGCTCTCCAGCCAGCAGTGCTTGATCAAGCCGAGCAGGCGTTGATCGTCGCGCGCACGAACGCTGGTGGGTTCGCGAAGCCATGCGTAGTAGCCGCTGCGGTGCACGTGCAGCACGCGACACATCGCAGCTAGTCCGAATTCGTTGGCGTGCTGCTTCATGAAGGCGTACTTCACCTTTACCCCTTGGCAAAGTACGCGGCGGCTTTTTTTAGGATGTCTCGTTCTTCAGTCACGCGCCGAAGTTCTGCTTTCAGGCGTCGCACTTCCGCGTTCTGGTCTTGCTCCACGCGACGAACCACGCCGCCTTTGCCTTGCTGGCGCTTCCAGCCGTACAGGCTGTGGACCGACACGCCCAGGCGCTCGGCTACTTCGGTAACTGGTCGCCCGTATTCCACGATCTGACGGACCGCTTCGATCTTGAACTCATCGGTGTATCGCTTCACGCTCATAACCACCTCCGCTTAAGCCATAGTTTATGGCTGCGAGATGTCTACGAAACCCTGGGCGATTCACTTGTTTGCCGCGCCCGTTGATAGAGGTGCGCCCACTGCGCCGGCGAGCACGCCTGCCAGACCTATTCCGAATCTTCCAGATTCAGAGTAGAAACCTCTTGACTCATAATAGTTTTGAACATTGCGGCAGAATTCGCTAGCTCGAATAAAGGCGTTCACCGCATCGGATGGCTCGCACTGCCGGTTCGGGCACGGCAATGCAGTCTCCGGCCAGGGCCAATTCACGACGCGTGATTGACTCAGCGTCGAGCAGCTACAGACGACAATGGCGAATCCAACGGCCATGCCAAGGCTTCTGAAGTCCATTTCTCACTCCCAGTGAAGGCAGCCGTCGAGGCGCTTGCGCGACGCAAGCCGTGGGCGACTCGTCCGCCGCAATGGCTTCAATAGAGCACACGCCAAACGGGGGCGAGTGCGGACAGCGAGATGAATCCTCTTCCGAAGTCTTAGTCGATGCCTATCCTGTGGCGTCCTCTCGTAGGCGTTTGATTGCACGCACCAAGTTGAAGACCCCCACTCCGTCAACGTGCTTCCTTCGCCCTGGGATCCGCTTCTCCCACCTTCCTGAGCCTGGCCAGAAGTCAACCGCCAGCGCCCTTCCAAGATGACCAGATGGGCGCCGAGCTCGTCCGCGTGGAAGGCAATGTTGTGTTCGTGAAGCACTCCTGGCGAATGCCGTCGGTTAAGTGCGTTACGGTAAGTTCGGTCTGTCTTCATCCGATCGGCATGCGACCGCATTAGAACTGAGTGAAGCTCCGGTTCCGCGCCGCTATGTCGCCCATAGAGGTGTCGCTGGAGAGTTAACTGAGCTGATGCTAGACCTTCAGCCACCAGAGTTCACCCGGTCGGCCAACTCAAGCGGTGACCGCATGCTGGGGCTATTTGCTTCCCGCGAGCCAGTTGCGGACCTCGTCTAACGTGGGGCCGAGGTTCCTGTCCGATCCCAACTCAGGCCGCCAATCCTGGGTCCAAGGACAAGTTGCCATTCGGACTGCTTCGATCGATGCATGTCCGCCCAGGTGTCCCCAAAGGGGCCCTCCACACGGAGCAGCTTCCGGTGAACCAGGCGCGAAGGCTCCCCCCATTCATCCGCCTCTCGCTCCTCGATCAGGACGGCTACGGCTTCGCCGTCCGCATAGAAGTCCGGCTTGCTGGTGCTCCGGAGTCGGCAGGGGTATCGGGAGATACAGATCGGCATAGCCGACGTATGGTAGCCGGACGCAAGTCACATTTTTGACTCGCCGGGCGTAAGATCTGGCCAGATCCAGCCGGAGACGAGCCATGTGCTATTCCGCCAAGGCCCGAGCCGAGTACCCGATCCTCACAACGAACCATTAGCCCTATCCCGCTCTATTGGTGAGACGAACAGCCCGCAGACGCCTCTTTTGCTGGGAATACATCTGCTGGGATAGGAGAGAATTTAGCGCAACGCCATAAACGCTTTCCGCCCCTAATGCCTCGCGAACCAAGGTCCACGTTCCGGCATCGCACCACCGTATATAACGCACATAGACAGATCTCCACGTGCCATATTCCTTCGGAAGTTCGCTCCAAAACGCACCATTGCATGCGACCCATAGGACGGCTTCGACGAAGCCACGATACATCTCATTCTTTCGTTTAGCCCGTGTAGCTAGATTAGGTGGAAGGACCAAACTGATCCTCAGCCAATCCGGCTCAGTCAACAAATCGACGCATCGGGCCACTACAACATTCTGACTCAT

Protein sequences of DBSCAN-SWA_2

>NZ_CP011130|5880788:5924616|5913386_5913617_-|WP_148650615.1|DBSCAN-SWA
MPIKTRQAKARASALRDELEVADSWHITSAERALRFSEQWDALVDQAPEEIRVELRRLGERIAANSPTFKRLPPSN
>NZ_CP011130|5880788:5924616|5893665_5896923_+|WP_057923066.1|DBSCAN-SWA
MTNRDTTITLLIKANATQLNQALEQAGVRARVFGNEAESAGRRAGKSFDSSRGSVEAIGRQLGQAKAQLLAFIGLQSAGTAIGGLVRAADGYANLSAKIKLATTSQASFNLAEDAVFAISQRTSTSLDTTATLFGRLSSALKDQGGSQREVLGLTETINKALAVSGATGAEASSTILQLSQAFASGTLRGDEFNSVNDAAPRLMKALAASMGVPIGELRKLAEAGKLTSEQLRVAFSGDQAKKIAAEFSQLPLTVERSLTQLDNAFTRFIGQQDRATGVSTAVAGSIQGLSQNFDSLANVVGVVVVAGLGRLIATLATAGAAKVAGIQKTQRLAQEELAQARAAETGAQAELARARALAMSGSGTARVAAAEGTLAAAQARTAAATQVATAAVGAKAVAVRALSSVLTLMGGPLGLAITGVTLLASAFASASANAKAAKVEFENTIKAAQRFREQQDIDTGVDAGKRLIAQREQLQKELSDLEGIQKGWGGGHFNEGQSSGRILYGAELDGEIKRVRSQLARTNDEFNQVRDSLTQLRAAQASGGRTRQQATKDVTDFTKALADQNEKLKIERIEREKGLRAALEYQAVKAAGVKDTAQLTEATRKAIDEQVRERDAAKASSDAGRAQAKAVRDAERQRKADERKLLRDQKEQERAGKKDTKDDEALSRTVQEADIALMRNRGEGAAARRKELDLEYKKALADLQAKGNTADALKIQLRIDTDVAKVELEDLQAQVDHVFGEQSRQEQSIQTRQQSGLLTEVGARRELIDLHARTAAEVEQLLPKMDALAAKTGTPESIERVKDLTAQAAALTLQSNELVVTLTNGFESGLSNALEGLATGTLTLRQALTGLVQDMAQSLAQLASQQLAALATAKLMSLVGKVAGGGKSPDVAQPDPVQAAAAGVAYATPITGASVALGVAGGIVLKAAAAMQTAAATMLAANASKSAAGFFASGGFTGIGPKYAPAGVVHRGEFVHRREVVRQPGARSFLERFNRLGMSALEGLRGYATGGFVSPAPRAPAPTRGPIADRTAPAAEGERRGSQITNVLYLDPREIVNVMSTQAGRQVILSTIRANAPTVRQDLG
>NZ_CP011130|5880788:5924616|5906312_5909348_-|WP_057923075.1|DBSCAN-SWA
MSHSIFNKALLALALVLPSAFNATAGEALILLSPAGPYYAPAAINVQIQCVSDDDFFPKTVKLYLDDALLRTSGCTVPDHALSLGRGHYNLRTVSTDAQGNTLNEAYSSFDVLIPGDFKPSVDLHQIPQGPYSAPATIPLSVTAADSDGQVVSVEYFANGQSIGTSTQTPFGLSWIGVAAGQYTVTAKATDNNSQTGTSQARTVTVGALSILGQIEGVRDNGAGGFDAYGWACLAGNAASIEVQFFARDPAPNGGMLIGTAQANQSGEPALSTACRTSANAYRFTFPLTEAIRRAHPNKKLYAYGVAAGASELIGQSGLHSIPGWQMLSRRFVYDQYQQLCKTIEPEIGATVMEYDGAGNLAWSAAGLTLPNATTCNRTDTQVSGRKVTRSYHQNNKLYQLKFPGGAGNQTWLYHPDGLPESVYTTNLVAPTTVINSYGYNKRRLPTGESNYSGDITYQHDRHGNVREANYSTRAFDYAPNALGQPTMVRDNAGQTYASAISYYPNGALKSFTYGNGIVHTMAQNARQLPARSTDAGIIDLESAFDPNGNVVQIYDRARGDHYNRSMQYDDLDHLQTVGSCSFGGDCWHRFSYDALDNLKSWSLGGVKDHRYYYDTRNQLTNVQNAQGASIVGLSYDPQGNLTNKNGRQFKFDYGNRLREVVGLDAYAYDAAGLRISVTRNGSTAEQSFYASGQLLRRDFPDSYIQNTYVYLGGSLIAQLERVPTDTGDTTRIKYQHTDALGSPVATTNEAGQVIDRTDWEPYGAAIGKPAYDGVGYTGHLVDGTTGLAYMQQRYYDQTLGIFLSIDPVTADGSTGANFNRYWYASNNPYKFKDPDGREITFAFKNGATVVDGIATMAYLAFSPTATNEIVRIQNSKELYTLSFDRSADAPFSYDRDTRTVNINPISGLRIKSSGEVQSPAIGASHEISHAAQHDRTSTESMRINLEAPVTKMEDTANGGFSVSFKSSPEENRAAAVEGKVAKELGEAPRKSYSDSKGTVVTCGPTSTKQC
>NZ_CP011130|5880788:5924616|5924232_5924616_-|WP_082648785.1|transposase|DBSCAN-SWA
MSQNVVVARCVDLLTEPDWLRISLVLPPNLATRAKRKNEMYRGFVEAVLWVACNGAFWSELPKEYGTWRSVYVRYIRWCDAGTWTLVREALGAESVYGVALNSLLSQQMYSQQKRRLRAVRLTNRAG
>NZ_CP011130|5880788:5924616|5917263_5917863_+|WP_148650616.1|DBSCAN-SWA
MGIHVSYHPFSPAEIHCLYFDIGRGACIERLVLQLGLDPAASATLKTLLSHGGRARPDGMSLSEAHAYNMDRVSGLLRDCWYTSNCRFSALLEHPGFCQYVTDWRNLMAEDVVHERCAHEKDLLRDDGIFFLSCGALKQLRAEHAEHGAVRSQLARVFPRGWLPIFWTAADHAVARECGLIEVVNLVHPDVITPSPLMA
>NZ_CP011130|5880788:5924616|5902602_5904762_+|WP_057923733.1|DBSCAN-SWA
MGLSRGPLDELVEIRVGDREAWKGSITKTGRIFINKPDLFGGDKGEGGIKGWLDVLMGEAAQAVLPALGALHGVPTPAFRNVTTQYFDGQIAANSPYPKPWKMRVRRALAGWDGAPWYPEKAVIWLANSAIRAMNPAHILVECLTNRDWGRGLDRGVLDDASYRRAADTLHAEGFGLCLRWNRQSSIADFMQVVIDHIGAAQYTDRSTGRLTLKLLRDDYRVEDLPLFDYESGLLAIEEDEGGAQDGAINQLIVTWYDPIKDEERQIRVEDLAGIQATGGVASSTTDYKGLPTPELAGRVGTRDLTIACSGLKRLKLRFDRRGGVLAPGGVFRIRDPFRGLDNLVLRVGTFDDGKLAEGAITVVAVQDVFGLPATAYLEPQPPVWTPPDRVPQPSPNRRLMEASYRDLATTLNAAALAAIPVDTGAVLAVAEQATGLALNYVLTTRVGSGEFTEAGAGDWCPTAVLADAMVATTVAVQLSSGRGLDQITAGTAALIEDEIVRVVAVNPQAQTATLARGCADTVPVPHAVGARIWFYDDFAANDPTDYSVGETVQAKLLTRTSSAQLDPALAPVDTIKLAQRQARPYPPGDLELNGLRYPASIDGDLAVSWAHRDRRLQADQLVDHGQGSIGPEAGTAYVVRLLDAIAGQALDSPATLTGANYASPLRGAYRVRAEIGSTRDGLTSWQKASHTFDFKNGLLRTEVGDDLVTEEGDYILAD
>NZ_CP011130|5880788:5924616|5888285_5888828_+|WP_057923059.1|DBSCAN-SWA
MDIFIDANAVLDTAKRVSEIPAKVAVSQRRALGTLRRRWPVIARRDIQAEYALSAQRIRAGVSVRTTREGVELVGVARGVGLRNFGTRKTEDGLSYSALRGKRGFRRKGFESRYRGTPIAFERTPISGDKRVPRTPIRRLYGPSLAQMLRKDDRPERMAQAGLDVITAEIDRLLLRSLRR
>NZ_CP011130|5880788:5924616|5902113_5902344_+|WP_057923732.1|DBSCAN-SWA
MWVQLAIWVISYFVSAAARPKPPQAKPAAFGDFQFPQSTEGTPQAVVFGDVWTPDWMVLGVGQYRTQPIKQKGGKK
>NZ_CP011130|5880788:5924616|5888882_5889641_+|WP_057923060.1|DBSCAN-SWA
MAAQDLFSFQGKVYLAQRQSNGKPGPLRWVGNAPQLQLTLEVQNSDKTESFSGNRMLYGRLVQSKTANVNLTLDEATPENIAEGLYSIPATLPAGAISNELLPPGLKANDLVALDRGWISELSLTDSATPPVTVPAANWWTESPSAGVIGLRKVDGHTQPFKATYQHGETVNIALFNTPPPERMLFLDGINTVNGRRAKVTLYRVAFNPIEQLDLISEEWGSLQLSGAALFDETRALDPALGGFGRIEMVRA
>NZ_CP011130|5880788:5924616|5890253_5890475_+|WP_057923062.1|DBSCAN-SWA
MKLIENWRQAWRFVSVQAMTVAIALQGVWLNLPDDLRIHVPDRITATVTAGLLILGLIGRLFQQRGADGTTLR
>NZ_CP011130|5880788:5924616|5919642_5920602_+|WP_082648784.1|DBSCAN-SWA
MHTELLPYWYPIARSEDVHDRPVRASLLENDLVLYRAGQQIVVAVDRCPHRGTRLSLGQHRDGALICPYHGLAFGLEGRCTHIPAHPHLTPSRQFQLSTYPAVERCGLVWTCLGTTPPPFPELSSDWDDPAFRQVAPDPVPIAASAGRQVEGFIDVAHFAHVHTTTFADPTNAAVPAYSVQVGEGRLRFDYCSTVSNYAVGSGMTADDFVWRRSFDVRLPYLAHLTVYFPNGRLNILNGASPVASDRTMLFSPVCFDLELGTDEAVKDFNARIFAEDRLMVENQQPRHLPLESGEASFAADLASVYYRRLLREMGLATA
>NZ_CP011130|5880788:5924616|5901276_5902092_+|WP_057923070.1|DBSCAN-SWA
MSFEQFERSTAAGNPRRLYEFVRGAKRWRYTGGDRAIALDTQIYDAVAISDDGIRQSGHTASDMLTITAPGDFEVARLYRGLPPSGEIAVVIRDIHETDDDAPVVWIGRIAGVNRPKLESTEVRCQSLDAALGQPGLRLAWTRGCPYTLYDRNCSANPESFRVPASLTTVAGNLVAAGVFGQYPDGWFAGGFLGWDLGEAGLERRGIRSHRGEWLTLLGAGDGLRVGQSVIAYPGCGRSMAICHNKFNNAPNYGGAPGIPGKSPFDGTPLF
>NZ_CP011130|5880788:5924616|5880788_5881340_+|WP_057923051.1|DBSCAN-SWA
MGISIRAYGRHRGVSDTAVRKAIAAGRITAEADGTINAARADAEWAASTRAPDAPLAATTRPARARAVNGPPVDDVGTVTPASAAGGGNTYAQARTANEVLKAQHHKLRIAQLKGELVDRSQVMAQVFALARAERDAWLNWPARISSMLAAELNIDPHVMHVALERGVRQHLAELGDFNARLD
>NZ_CP011130|5880788:5924616|5883286_5883505_+|WP_057923053.1|DBSCAN-SWA
MTDLPYTYEQLKALRNALARGERRVSFGDRLVEYRSVDELLAAIREIEAALAGTEGQPRRPRRLLTTTGKGF
>NZ_CP011130|5880788:5924616|5887953_5888286_+|WP_057923058.1|DBSCAN-SWA
MSVALEPAQHPDEEAIGLTLASLGIQRDANKPHGRHRLLQGLAEATLPASLADAHAQCHAIAADIEDALDDWIPLPNALPVQVEDIVFLDRPEGLPVVAVQVALTIRYRR
>NZ_CP011130|5880788:5924616|5904773_5905205_+|WP_148650613.1|DBSCAN-SWA
MKLSQLPAATALTGSEILPVVQAGQTRSTTVAAMADLRKGAWQVPSLNAPWTNYGDAFANTAYRKDGNRVQLRGLVKAGAGGSMIFTLPAGFRPPAQQIYVASCDATTPARVDVRSNGDVVIAQPATGTLGWLSLDGIAFFAD
>NZ_CP011130|5880788:5924616|5916962_5917205_+|WP_057923078.1|DBSCAN-SWA
MAGKPRFEVYREGRRAGGQRSLSNDFLAGSATDGQWRWRLVGGNGEPMAHGESYPDKGSMLRTIDIIANLDGAEIREVDG
>NZ_CP011130|5880788:5924616|5886174_5886567_+|WP_057923056.1|head|DBSCAN-SWA
MRITTYPPFQEGLNLGDLLKFEADNLYSRDQVTIAPNQSLVLGQIVGRVSGSNHVAAFDPAATDGREIAIGVAIVPITTTKDASPDGLIIARHAAVADHALVWSAAITPEQHAAAVEQLRALGVLVRHGV
>NZ_CP011130|5880788:5924616|5902340_5902562_+|WP_057923071.1|DBSCAN-SWA
MIVTLDHLRRAPGFGVRSGFCAQGGREWFAYYGLDWSAFVRDGIEAEAIEATGDALGLHLIAFARAEAARGQQ
>NZ_CP011130|5880788:5924616|5897051_5898629_+|WP_057923067.1|DBSCAN-SWA
MTLRTGVASDYYDFLNQLEAALCREGHAWGLLYAGAGNGALTGVDGGSGGYRGGTGSLAEAFTLTALDAQRFQVVGALAGDLGVATVAQPFEHERLRFRINAGSTAFAAGDRFTLNTSPPWTLVRRCGVRNPSFRTGNFTNLSALFDNAMDTWATRAVTDLPAIARIEMIGPAAVRAVTMGIGDSGARGAAAFELQRSDDGAAWSPVQTWSGVRWPSARARQTFLVAGNPPAARFWRVVFSATNGATPLDCNDLSFHFDLNADFELEDRAQWIVKAPGLDGRQSIFIGAELFEEPARAAYNLNWYGLRSHNPLLSLRSQVNNSGLRHLPLRNGPFAYWLAINGQRIVIVARIGTVYVSAYLGFATAYEPPSIHEYPLIIGACGSTENGTPDATDANFRGFFDPGRYALMANYPDNVWRPHCNRYASGTNDYGDTETAGKVYPSAMSTGGDRAYLRDNLDGSSPLFPLILGAAQPRHGWGEFDGCAWTTGFSTASESRIERDGATWLAFQNAFRISPDNYFALKMD
>NZ_CP011130|5880788:5924616|5918384_5919653_+|WP_082648783.1|DBSCAN-SWA
MIGTLLDFASDMARWLHVLAAFAWLGGGMWVRRLTLRAKPLLDQRAELEVWDTHSLSFWRSSKVSAPTAAELDGLVWSFNQIRWLIGTGVVLFGLIYYRQPLAYLIDPSIARLSARDAIEISALGLIGAPLLNELVNRIPLRHKTLYMAATIAHLLGWVWLYANLFSQHGAMIQIGAMLGVVIASNVIWWLYPRMRKAYDAVLKGDQPDPIDRLLWDRRGLHAHITFAVVFLMLSSHMGSLVRANGHPFLTISTVLALSVGARWVFDVTHRNGGVMPIKQRWMSVAAVLVVGLGMTWMALPELPTEQVVAHANAPAPASIAAQPVKHSSPSSIASSIVSGTIPLRADAIVQRRCAVCHAAQPSFPGIASPPKGIVFTSETLPLYARLIATVVQSERMPPGNATDMLPEERKAVTQWATEHAH
>NZ_CP011130|5880788:5924616|5905344_5905740_-|WP_148650614.1|DBSCAN-SWA
MKSINVTLVALVLTSCSAIPTKSSDALTPSMLNAMMSEHHGQRVKVFGWMTSSFERYGLWESRAAFDRGNYADDCISLLIPEVMDTSLYDRRYVELEGNFIQRPEENTINLGACNKTTIILSAESPPELVK
>NZ_CP011130|5880788:5924616|5890928_5891318_+|WP_057923064.1|DBSCAN-SWA
MIALKVWATTLLSALAAVLVAFGWGRWKGRQRERTDTAARVAESEQRVRVAERERADSEIRTEVDTDVLHLPTGILAPVADAVPDSAADRLYDDWSRDGSNDGLRLDAADPGLAGGSTDRSDGATNPGA
>NZ_CP011130|5880788:5924616|5881343_5883290_+|WP_057923052.1|terminase|DBSCAN-SWA
MYDGFDDVARFWRDGLTPDPFLDVSDWADRDRVLSSTSSSEPGRWRTARTPYLRDIMNDLSPASATERVVFMKGAQVGGTECGNNWIGYVIACAPGPMMAVAPTVEMAKRNSKQRIDPLIEESPSLRERIAPSRARDAGNTILAKEFRGGVLVLTGANSAVGLRSMPVRYLFLDEVDGYPRDVEGEGDAVALAEARTRTFTRRKILLVSTPTIAGASTIEREYLASDQRRYFVPCPHCAEMQWLRFEQLRWTWGDSRSARYICEGCEQPIGEHHKTAMLAGGEWRATAPQNKGKTAGYHLSSLYSPVGWRSWADIAAAWESAQGSATALKAFKNTELGETWEEEGEAPDWERLQERREDYRVGTVPAGGLLLAGGADIQKDRIEVSVWAFGRGRETWLVEHRVLMGDTARAAVWNELGAVLSQHWTHASGALLPLTRMGLDTGYATQEAYAFARGVQDPRLLPMKGVGSGAALIGTPTAVDVSVPGKRIRRGLKLFAVAGGIAKLEFYNALRLPIEIGPDGQPAFPAGYVHLPKIDGEFLQQLTAEHLITRRDRHGYPQRVWEKRRDRNEALDCYVMARAAAMQAGVDRFEERHWRELERTLGMQPNEPPAIPRQPPPYPTPQAAPLGGLSVSDPRRVRRVISSRFMR
>NZ_CP011130|5880788:5924616|5890455_5890932_+|WP_057923063.1|DBSCAN-SWA
MARLSAEQAGGQNVVAFLDMIAHAEGVERFSEHGGYDVLVGGKTFTSYVEHPRKLVWLPKYRINSTAAGRYQFLWKTWNSLRNRLRLPDFGPASQDRAAIELLRETGALADIKQGWISSAVRKSRKTWASLPDAGYGQREVPLERLLAVYQKAGGQIA
>NZ_CP011130|5880788:5924616|5914170_5916609_+|WP_082648782.1|DBSCAN-SWA
MKNTAKQECKTLSEQNWSLSTFTEFYERVLGPRLFKPYGELLAHEICKDIDPDAPPSSILEVACGTGRITAALYQDLAKPLGLQLVATDLSKIAIEMAKNVLGEELQRDVAFHSDVDMADLPFADNSFDVVVCGFGLMFPPDKARVAREFKRVLRPGGKIYGTVFQYNELFDLALKQSQKHFGAPSAIMGAALSLTDPSAITRAFSLEGLSPGIGEVATSRALSFFLDDLDTREFLFNACILLEEFNQCDAPTREAYLDAMLQEFHAQIPSRNYQVKAWLLRGEVGQACKESVVPSPPPNFSELSDFCRIPPAPIGSDADSPFSPQAERSLRPYRTMKRVFLAEHPDYPEADVEALRKSEFSRLDALQTTYLDHVGGTIAPDSLIEQDYRVLKNSILGNPHTGSKSSDGAHEKARAEIYRFFRCSQDEYEIIFTPNASGAIRLIAESFPFESGSQVLLTKDNHTSVHGLREYARAKGASVKYIPLDNELRIIESSMQRSLDGLVSGRLHLLAYPAQSNATGARHDLKWIGLAQERGAMVLCDAAAFVPQSRLDCSVHRPDFVAISFYKIFGHPTGTGCLIARRSALRELTPPSFSGGSVCYYSGPWSPTDRLLHREDGKRFEIGTPNYASFDAIALGFQFVSRLGLERISARSSALARWLEARLQELRHDIKSQTPLCRVYGPSAEHKGATVMLNFFDCYNAVFPHALVKRTAESFGIVVRNGCFCNLGAVQQATYTTAGAEHCELDKTEKILDCKAFDDNILNKGNCGAIRVSFGLGSNFRDAYCFYLFAKCLLNTECARLEDALAGSSVN
>NZ_CP011130|5880788:5924616|5912651_5913266_+|WP_187313286.1|DBSCAN-SWA
MIRIFVVDDHPLLRIGLRWLLEAQGDIQVIGEAGSVADAMIMIPAAGPDLVLCDFHLPDGDGLDVAQRLLQERPNLRILVVSVLEGGPIPRRLLAAGALGYVSKARDGATLLRAVREVAAGHRFLDEALAASILFEPSPFDRLSPRELEVARMMVRGEKTPAIAEALGITESTIRTFRARVLAKLDVHSEISLIRLAMDCGFEK
>NZ_CP011130|5880788:5924616|5891552_5893229_+|WP_057923065.1|DBSCAN-SWA
MRTVASRCWSSLLLILLALCASGAHAASLRLERLDRQSAQPEEVLAGAYDQEFRKVDGPSIVIPRPAPQWWRVVLGDLPTDRALPQLVLSPPNQKRLEVWQPGEQMPISRSAFGPESELLHSARALVVPLNAGLKPGDVVYLRITSPNLIASELSVQPMATVHADDVYYARFRASVLVALFIVALMSFGYFAALREHGYAYLGITLLAQLANLVIEGGEVRVFPALAEFAMDRRTNIVINTAAVLTGIRFLMFFLQLQIQQPRVAKLLNVCSVMLGGLLLASVVHVTTFSAYFGNTVMLVAFGGIAVAICRGLRRRQLDAMYLLIAWAPVMVVLVAMVGGYQDWWAMPGWAIDGFPIGVAASGLGLMLGLTARLEQVRVDRDAAQRRWTYDKLTGVITRDAVEDMLRVNIEKAHAAGSPLSVVFVDIDHFKSINDLHGHSTGDEALRIVALRIRNWLPAGHLVARYGGDEMLLVLVGLNQREALVLAGALRETVSRNPLAIDGIVVPLGLSMGVADLQPGDSSQTLLRRADAALYRSKASGRARVTGYGVDGEIEGAG
>NZ_CP011130|5880788:5924616|5887652_5887898_-|WP_148650612.1|DBSCAN-SWA
MRWSNSHVGAVSAMQHRLVDEAVVRYERFDDLNAPVERDFIAATEHPLTISSGYVPCAANDLLEFPKTLDAVAHYKRDAGR
>NZ_CP011130|5880788:5924616|5909414_5912153_-|WP_187313285.1|DBSCAN-SWA
MSKVLSLSTLALLCACASALAQSPLMPPVEYEKRIRATEMVTALSSGLFGDSVSLYNGSTEFAVTDIDIPGNSSLPVRLSRRFKVEAKKEVVNLGGFGAWDIDVPYVYGTFPANTQWNEGSRPTDNRCSNNWLPKIPFNHRLRDIWQGNFVHLPGGGDQEMLVLGTTGNAVPNDGQTYTRSTRDGMRFRCVANGVNNYPGEAFVGVDTSGTKYFFNTMAYRGAGAMKGTPTRPGFGRIRVYLMATRVEDRFGNGVNYNYGGSQGGQLLSVVADDGRRIDLEYDGGATVQRARANGRVWQYGYTGGGGALGINRFPLLASVTLPDQSAWTYSYNMPMQYGGLNPNYTPLDVDGGSCAEPDFGPETFTLTAAHPSGAVGTFVMPYTRLHRFGTPASACVPALENTNGNPDGPHELLISDYFDVYALARKTVTGTGGIAHEWTYDYGDMGIGRIDGPLQICPGCSVAKTVTVRNPDGSLTLHDFGYIYEYNDGQPLGTRTVSADNKVLRSESSEYVQYSNGTTMPFPWFYGELLGGDDSTSSMVRPLKKKIIVQDGATFTWQVDGSCTGTTGLCFDQFARPTKVIKSNTLGFSKNDTTEYRDGMTRWVLGQVQRSTTNGIETDRTEFHATTDLPIKGYAFGKLQQTVSYNADGTIATAADGNTNVTTFSNWKRGLPQSVTYADGTATSAVVDDNGWIRSVTDENGYAKTYDYDAAGRLVKIVYPTGDTVAWYDTVLRFEPVAATEVGLTAGHWRQTVTTGNRKKTTYFDALWRPVAEQEEDTSNPQATTRWSAKRYDHDGRVVFASYPRNPFVDGVVNFDSAMSGTSTSYDALGRATEVRQDSELGVLRTVTEYLPGMQQKVTNPRGKSVVTRYQAFDAPSYSLPIEQNLPTDAATYIRRDVFGKPLEIRRSGAP
>NZ_CP011130|5880788:5924616|5898628_5899564_+|WP_057923068.1|DBSCAN-SWA
MAYATSAANDPNELLDKLRLFAQSAGWSIDGLRDRPANAGKALSLHAGNVYATFVSQLAGGDGNSPAPFLGSFGHTGYTANPNPDIQADASSIVWANYVQGPYSAVHFFGRIAPQPYLHIVLETQAGTFKHFGTGRLITAGVVNTGQYIYGSQWYYSATYINSPDSPYHSVAFDDTYYNYTAPCTRIRADFEGIAPRWHATSGDSNDSRRLLAGWRGKTAPINLLKDVGHSTLTGRAPGQPLWCAVPRGAGLFSDVGHPPDMRFIRLDSYAPGEELPLGTDRWKVFPVHRKNGPPGAPNSGVYGYAYRISE
>NZ_CP011130|5880788:5924616|5899576_5901280_+|WP_057923069.1|DBSCAN-SWA
MIWPALWPLTFSGQGDYFKSPPFWNGQASGALGAEPGFGRRAVDVPGFVADRRVGAPQAMFGDDFFDRIHIEPQVLNLGNVSSVQQRAVRVWNAYRARALTLTEAALSGGEGIVLTAPGATPLPFAPMSERTWQIAVGTDGPPVISATLSFRFDGFAAIPVVITGQRIVAWAFAPDWSRGVLERLAWKTDILTSPTQVEQRRGLRSAPRRSFEATMIVDGRERVLLDLAVFGWGGRTWALPIWPDVQWLSTEHALGVRVIACDPRHRDFRVGGLVQLRGKTAFDVEVAEVEAIGGASITLRHPTTMAWPLGTRLYPVRTARLAEPPRVTRLTDQAASVSARFDVVEACDWPVVTDAPLYRGHPVLAQRPDETESLSNGWQRMLLTLDNEFGRPFVLDPADWAAPTQSHQWRMHGRIERAAVRSWLYTLRGRQQAVWRPTHADDLTLVANVAGTATALDVANVGLARFSGLRLGRRDVRIELRGGQAFHRRITAAVALDDDIERLTIDAALGVDMRPRDVQRISFLVLSRGDSDEAEIEHHTDSDGAADASIILRAVRDPDTDTPAPA
>NZ_CP011130|5880788:5924616|5884997_5886173_+|WP_057923055.1|DBSCAN-SWA
MTGLPHLAARVFNTPLLIQRAKLEVILSVLAPKFELQTLPPPQMGPPMPAPALANEQGIYVLPIHGTLVQRAVGLDALSGLTSYVSIARRLDAALADDSVRGIVLEIDSPGGEAAGVFDLADKIRAASAAKPIWAVANDAAFSAAYALASATNRLFVTRTGGIGSIGVIALHVDQSQSDANAGLKFTPIHAGARKNDGTPHEPLTDEARGSIQTEVNRLYELFVLTVADQRGLSAEAVRKTEAALYFGQDAINVGLADRLGTLSDAVQQMHTELDAAARPLFLENPTMSLPDATVPTVDTDAVRAQSRADSLAIAELCELAGQPQLTAALLAEGVTPAVARQRLLAAKAESTEITSHLSPNAPTPSMATSLDDNPLVQAVKARAAATRKER
>NZ_CP011130|5880788:5924616|5921687_5922829_-|WP_148650586.1|transposase|DBSCAN-SWA
MSVKRYTDEFKIEAVRQIVEYGRPVTEVAERLGVSVHSLYGWKRQQGKGGVVRRVEQDQNAEVRRLKAELRRVTEERDIPKKSRRVLCQGVKVKYAFMKQHANEFGLAAMCRVLHVHRSGYYAWLREPTSVRARDDQRLLGLIKHCWLESGSIYGHRKITKDLRELGETCSKHRVARLMKQEGLRAMVGYGRRPRPLNGPIGAVANNVLARAFTAAEPNRTWVTDITYIRTYEGFLYLAVVLDLFSRQVVGWATRPTQHTDLVLQALLAAVWRRKPEPGLLLHSDQGSQFTSEDWQSFLKAHGIVCSMSRRGNCHDNAAMESFFQLLKRERIKQRIYNTHADARGDVFDYIELFYNPKRRHSSNDGLSPIEFERRYALNG
>NZ_CP011130|5880788:5924616|5920717_5921680_+|WP_187313287.1|DBSCAN-SWA
MDALIDFMTDIVRWLHVVAAIAWLGFVLWLRRLAIRARSVLDSSADLEVWDTHSLGFWQTERITRPKASDLEGLVLSFNLIRWLFGTGLLLFSLIYYRQPQVYLLLDPSDASLSSHAAIALSLAGLIGAPLINETINRIPLHRTILYYVACALHVLAWMSFYADRYSQHGAMIQIGAMLGTTVSVNILGNLYPATRAAMVAVMRGEQPDPIRKQYWDRRNQHSFLLPAIVFLMLSSHMGSAIKANGHAFATIVIVLALSVASRHVIEMVHRNHGIVPTRLRWAGVAAALALVLALAWLVVIEHQVNLPATADATESPRLL
>NZ_CP011130|5880788:5924616|5889640_5890072_+|WP_057923061.1|DBSCAN-SWA
MARKVQRPKPPADELTVLQPNRMLPLGDRTVTVREIGFFESLRLHAQIAALVADLIEQTDDGNIDLGRLHRVCAQHPEATVELLAQASDQSVEFVHSLSAAHGDLLLLTFWAVNADFFLQRVIAALELRRADPATTGPASSPP
>NZ_CP011130|5880788:5924616|5886576_5887578_+|WP_057923731.1|capsid|DBSCAN-SWA
MNNPFHNPAFSMSALTTAINILPNQYGRLDELNLFPIKPVRTRQVTVEERNGVLSLLPTQPVGSPGTVGKRGKRALRAFNVPHIPHDDVVLPEEVIGVRAFGSESELQTVAGVMADHLQTMRNKHAITLEHLRIGALKGVILDADGSELANLFDIFNIAPKTFDFQLSNPNTDIKKKCLDLKRYMSKVLLGERMTGIHVLVSPEFFDAFTGHDAVKDAYRLWQDGLVLREDMRSDFRFAGIRFEEYIGEVSDGEGKTRRFIEEGEAHAFPLGTMDTFATYVAPADFNESVNTLGQLLYSKQEPRKFDRGTDLHTQSNPLPMCHRPALLPKLKM
>NZ_CP011130|5880788:5924616|5883504_5885001_+|WP_057923054.1|portal|DBSCAN-SWA
MSWWSRVRTAMFGGSPVHEVAGHGRRSTAWQPSNPGAIAALVATGDALRVRSRDLVRRNAWANAAIEAFVANAVGTGIKPQSLIADQTQREALHALWRDFVDEADAAGLTDLYGLQALGCRALLEGGECLVRLRPRRPEDGLAVPLQLQVLEPEHLPLTLNREEPNGNVIRAGIEFNRLGRRVAYHLYLSHPQDGSMAPMSRQGGLDTFRVPATEVLHIFRPLRPGQIRGEPWLARALVKLNELDQYDDAELVRKKTAAMFAGFITRDGPEDPLPGDAPPDEHGNAPLGLEPGSLQILEAGESVTFAQPADVGASYDAFLRSQFRAVAAAMGITYEQLTGDLTGVNYSSIRAGLLEFRRRCEMVQHSVLVFQLCRPIWNAFVDAAVLSGAIELTGYRRRKRQYRACKWVPQGWSWVDPEKEFNAMILAIRAGLLSRSEAIASSGYDAETIDREIAADAQRADALGLVLDTDPRAVARNGVKHAPPQADSAAFDTKPTE

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_057923051.1|5880788_5881340_+	hypothetical protein	A0A2H4JCL4	uncultured_Caudovirales_phage	2.3e-49	62.8
WP_057923052.1|5881343_5883290_+|terminase	phage terminase large subunit family protein	A0A2H4JIC6	uncultured_Caudovirales_phage	3.5e-257	68.8
WP_057923053.1|5883286_5883505_+	hypothetical protein	A0A2H4JCJ9	uncultured_Caudovirales_phage	1.2e-12	59.4
WP_057923054.1|5883504_5885001_+|portal	phage portal protein	A0A1B2LRR5	Wolbachia_phage	1.8e-141	55.6
WP_057923055.1|5884997_5886173_+	S49 family peptidase	K4HZZ6	Acidithiobacillus_phage	7.9e-71	44.4
WP_057923056.1|5886174_5886567_+|head	head decoration protein	A0A1B2LRT0	Wolbachia_phage	4.1e-24	51.7
WP_057923731.1|5886576_5887578_+|capsid	major capsid protein	A0A1B2LRS0	Wolbachia_phage	8.9e-116	69.5
WP_148650612.1|5887652_5887898_-	hypothetical protein	NA	NA	NA	NA
WP_057923058.1|5887953_5888286_+	hypothetical protein	NA	NA	NA	NA
WP_057923059.1|5888285_5888828_+	hypothetical protein	NA	NA	NA	NA
WP_057923060.1|5888882_5889641_+	hypothetical protein	A0A0S4L1I6	Pseudomonas_phage	1.3e-58	48.6
WP_057923061.1|5889640_5890072_+	hypothetical protein	NA	NA	NA	NA
WP_057923062.1|5890253_5890475_+	hypothetical protein	A0A0B5A601	Paracoccus_phage	2.2e-06	34.3
WP_057923063.1|5890455_5890932_+	glycoside hydrolase family 104 protein	Q9MC90	Pseudomonas_phage	6.3e-35	49.4
WP_057923064.1|5890928_5891318_+	hypothetical protein	NA	NA	NA	NA
WP_057923065.1|5891552_5893229_+	diguanylate cyclase	G3MA91	Bacillus_virus	2.2e-13	31.4
WP_057923066.1|5893665_5896923_+	tape measure protein	B7SE05	Pseudomonas_virus	1.4e-32	30.5
WP_057923067.1|5897051_5898629_+	hypothetical protein	A0A2D2W2B4	Stenotrophomonas_phage	4.0e-110	41.4
WP_057923068.1|5898628_5899564_+	hypothetical protein	J9SVR7	Pseudomonas_phage	6.3e-23	32.1
WP_057923069.1|5899576_5901280_+	hypothetical protein	Q5ZQW3	Pseudomonas_phage	2.3e-143	52.7
WP_057923070.1|5901276_5902092_+	phage BR0599 family protein	J9SN93	Pseudomonas_phage	1.1e-60	42.8
WP_057923732.1|5902113_5902344_+	hypothetical protein	Q6UYJ6	Burkholderia_phage	1.2e-20	64.9
WP_057923071.1|5902340_5902562_+	hypothetical protein	H6V8R0	Pseudomonas_phage	1.1e-13	52.8
WP_057923733.1|5902602_5904762_+	hypothetical protein	Q5ZQV9	Pseudomonas_phage	1.6e-202	52.8
WP_148650613.1|5904773_5905205_+	hypothetical protein	NA	NA	NA	NA
WP_148650614.1|5905344_5905740_-	hypothetical protein	NA	NA	NA	NA
WP_057923075.1|5906312_5909348_-	RHS repeat-associated core domain-containing protein	NA	NA	NA	NA
WP_187313285.1|5909414_5912153_-	RHS repeat protein	NA	NA	NA	NA
WP_187313286.1|5912651_5913266_+	response regulator transcription factor	NA	NA	NA	NA
WP_148650615.1|5913386_5913617_-	hypothetical protein	NA	NA	NA	NA
WP_082648782.1|5914170_5916609_+	aminotransferase class V-fold PLP-dependent enzyme	NA	NA	NA	NA
WP_057923078.1|5916962_5917205_+	YegP family protein	NA	NA	NA	NA
WP_148650616.1|5917263_5917863_+	hypothetical protein	NA	NA	NA	NA
WP_082648783.1|5918384_5919653_+	urate hydroxylase PuuD	NA	NA	NA	NA
WP_082648784.1|5919642_5920602_+	aromatic ring-hydroxylating dioxygenase subunit alpha	NA	NA	NA	NA
WP_187313287.1|5920717_5921680_+	urate hydroxylase PuuD	NA	NA	NA	NA
WP_148650586.1|5921687_5922829_-|transposase	IS3 family transposase	U5P429	Shigella_phage	1.6e-92	61.7
WP_082648785.1|5924232_5924616_-|transposase	transposase	NA	NA	NA	NA