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_CP023445	Actinosynnema pretiosum strain X47 chromosome, complete genome	17 crisprs	cas3,DinG,DEDDh,csa3,cas4,WYL,cas6e,RT	0	19	2	0

1. NZ_CP023445

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP023445_1

• CRISPR_ID: NZ_CP023445_1
• CRISPR_location: 30133-30630
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 8 spacers

Consensus repeat of NZ_CP023445_1

Consensus_repeat	Method
CTGGTCGTAGCCNNGCTGCTG	CRT

spacers of NZ_CP023445_1

>1.1|30154|45|NZ_CP023445|CRT
GCCGTAGCCCTGGTCGTAGCCCGCGGCCTGCTGGCCGTAGCCCGC
>1.2|30220|57|NZ_CP023445|CRT
CTGGCCGTACCCGGCCTGGCCGCCCTGGTCGTAGCCGGCGCCGCCCTGGCCGTAGCC
>1.3|30298|33|NZ_CP023445|CRT
GCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCC
>1.4|30352|27|NZ_CP023445|CRT
GCCGCCGTAGCCGCCCTGGCCGTAGCC
>1.5|30400|33|NZ_CP023445|CRT
GCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCC
>1.6|30454|21|NZ_CP023445|CRT
ACCGCCTTGGCCGTAGCCCTG
>1.7|30496|42|NZ_CP023445|CRT
CTGGCCGTAGCCCTGCTGCTGACCACCTTGGCCGTAGCCCTG
>1.8|30559|51|NZ_CP023445|CRT
ACCGCCGTAGCCGCCCTGCGCGTAGGGGTCGTAGCCGGGCTGGCCCTGTCC

CRISPR arrays and Neighbor proteins around NZ_CP023445_1

CRISPR arrays

The CRISPR arrays of NZ_CP023445_1

>merge|NZ_CP023445|1|30133-30630|CRT
GCCGCCGTAGCCCGCCTGCTGGCCGTAGCCCTGGTCGTAGCCCGCGGCCTGCTGGCCGTAGCCCGCCTGGTCGTAGCCCGCCGCCTGCTGGCCGTACCCGGCCTGGCCGCCCTGGTCGTAGCCGGCGCCGCCCTGGCCGTAGCCCTGGTCGTAGCCCTGCTGCTGGCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCCCTGGTCGTAACCGGGCTGCTGGCCGCCGTAGCCGCCCTGGCCGTAGCCCTGGTCGTAGCCCTGCTGCTGGCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCCCTGGTCGTAGCCCTGCTGCTGACCGCCTTGGCCGTAGCCCTGCTGGTCGTAACCCTGCTGGCCCTGGCCGTAGCCCTGCTGCTGACCACCTTGGCCGTAGCCCTGCTGGTCGTAGCCAGGTTGCTGACCGCCGTAGCCGCCCTGCGCGTAGGGGTCGTAGCCGGGCTGGCCCTGTCCTTGTCCGTAGCCGGGAGGCTG

>NZ_CP023445|1|1|30133-30630|CRT
GCCGCCGTAGCCCGCCTGCTG	GCCGTAGCCCTGGTCGTAGCCCGCGGCCTGCTGGCCGTAGCCCGC
CTGGTCGTAGCCCGCCGCCTG	CTGGCCGTACCCGGCCTGGCCGCCCTGGTCGTAGCCGGCGCCGCCCTGGCCGTAGCC
CTGGTCGTAGCCCTGCTGCTG	GCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCC
CTGGTCGTAACCGGGCTGCTG	GCCGCCGTAGCCGCCCTGGCCGTAGCC
CTGGTCGTAGCCCTGCTGCTG	GCCGTAGCCCTGCTGGCCGCCCTGGCCGTAGCC
CTGGTCGTAGCCCTGCTGCTG	ACCGCCTTGGCCGTAGCCCTG
CTGGTCGTAACCCTGCTGGCC	CTGGCCGTAGCCCTGCTGCTGACCACCTTGGCCGTAGCCCTG
CTGGTCGTAGCCAGGTTGCTG	ACCGCCGTAGCCGCCCTGCGCGTAGGGGTCGTAGCCGGGCTGGCCCTGTCC
TTGTCCGTAGCCGGGAGGCTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096490940.1|27881_29306_-|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|223704
NZ_CP023445.1|WP_096490947.1|39088_39856_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|187593
NZ_CP023445.1|WP_012782665.1|31712_32333_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096490945.1|35776_36442_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380058
NZ_CP023445.1|WP_096490935.1|20411_21053_+|aminodeoxychorismate/anthranilate-synthase-component-II	unknown	unknown	gnl|CDD|181107
NZ_CP023445.1|WP_096490937.1|23293_24952_-|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP023445.1|WP_096490944.1|34592_35780_+|amino-acid-deaminase/aldolase	unknown	unknown	gnl|CDD|143488
NZ_CP023445.1|WP_096490948.1|40604_40928_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096490942.1|32383_33019_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187554
NZ_CP023445.1|WP_012782673.1|40228_40591_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096490936.1|21167_23213_-|Stk1-family-PASTA-domain-containing-Ser/Thr-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP023445.1|WP_096490934.1|18999_20346_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|215457
NZ_CP023445.1|WP_096497529.1|18013_18793_+|class-E-sortase	unknown	unknown	gnl|CDD|320679
NZ_CP023445.1|WP_096497530.1|37925_39092_+|MFS-transporter	unknown	unknown	gnl|CDD|340883
NZ_CP023445.1|WP_096490946.1|36528_37788_+|family-1-glycosylhydrolase	unknown	unknown	gnl|CDD|274539
NZ_CP023445.1|WP_096490932.1|17104_17371_-|cell-division-protein-CrgA	unknown	unknown	gnl|CDD|178907
NZ_CP023445.1|WP_096490939.1|26414_27878_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	unknown	unknown	gnl|CDD|223843
NZ_CP023445.1|WP_096490943.1|33231_34509_-|FAD-binding-protein	unknown	unknown	gnl|CDD|130740
NZ_CP023445.1|WP_012782663.1|29302_29767_-|FHA-domain-containing-protein	unknown	unknown	gnl|CDD|224630
NZ_CP023445.1|WP_096490938.1|24951_26418_-|penicillin-binding-protein	unknown	unknown	gnl|CDD|274573

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096490940.1|27881_29306_-|serine/threonine-protein-phosphatase	gnl|CDD|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	1.99555e-76
NZ_CP023445.1|WP_096490947.1|39088_39856_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|187593	cd05332, 11beta-HSD1_like_SDR_c, 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1)-like, classical (c) SDRs. Human 11beta_HSD1 catalyzes the NADP(H)-dependent interconversion of cortisone and cortisol. This subgroup also includes human dehydrogenase/reductase SDR family member 7C (DHRS7C) and DHRS7B. These proteins have the GxxxGxG nucleotide binding motif and S-Y-K catalytic triad characteristic of the SDRs, but have an atypical C-terminal domain that contributes to homodimerization contacts. 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 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	3.42004e-52
NZ_CP023445.1|WP_096490945.1|35776_36442_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|380058	pfam17928, TetR_C_22, Tetracyclin repressor-like, C-terminal domain. TetR family regulators are involved in the transcriptional control of multidrug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. The TetR proteins identified in overm ultiple genera of bacteria and archaea share a common helix-turn-helix (HTH) structure in their DNA-binding domain. However, TetR proteins can work in different ways: they can bind a target operator directly to exert their effect (e.g. TetR binds Tet(A) gene to repress it in the absence of tetracycline), or they can be involved in complex regulatory cascades in which the TetR protein can either be modulated by another regulator or TetR can trigger the cellular response. TetR regulates the expression of the membrane-associated tetracycline resistance protein, TetA, which exports the tetracycline antibiotic out of the cell before it can attach to the ribosomes and inhibit protein synthesis. TetR blocks transcription from the genes encoding both TetA and TetR in the absence of antibiotic. The C-terminal domain is multi-helical and is interlocked in the homodimer with the helix-turn-helix (HTH) DNA-binding domain. This entry represents the C-terminal domain present the TetR Transcriptional Repressor present in sco1712 proteins from Streptomyces coelicolo which act as a regulator of antibiotic production.	2.9158e-26
NZ_CP023445.1|WP_096490935.1|20411_21053_+|aminodeoxychorismate/anthranilate-synthase-component-II	gnl|CDD|181107	PRK07765, PRK07765, aminodeoxychorismate/anthranilate synthase component II.	1.79652e-127
NZ_CP023445.1|WP_096490937.1|23293_24952_-|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.45025e-109
NZ_CP023445.1|WP_096490944.1|34592_35780_+|amino-acid-deaminase/aldolase	gnl|CDD|143488	cd06813, PLPDE_III_DSD_D-TA_like_2, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes Similar to D-Serine Dehydratase and D-Threonine Aldolase, Unknown Group 2. This subfamily is composed of uncharacterized bacterial proteins with similarity to eukaryotic D-serine dehydratases (DSD) and D-threonine aldolases (D-TA). DSD catalyzes the dehydration of D-serine to aminoacrylate, which is rapidly hydrolyzed to pyruvate and ammonia. D-TA reversibly catalyzes the aldol cleavage of D-threonine into glycine and acetaldehyde, and the synthesis of D-threonine from glycine and acetaldehyde. DSD and D-TA are fold type III PLP-dependent enzymes, similar to bacterial alanine racemase (AR), which contains an N-terminal PLP-binding TIM barrel domain and a C-terminal beta-sandwich domain. AR exists as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Based on their similarity to AR, it is possible members of this family also form dimers in solution.	0
NZ_CP023445.1|WP_096490942.1|32383_33019_+|SDR-family-oxidoreductase	gnl|CDD|187554	cd05243, SDR_a5, atypical (a) SDRs, subgroup 5. This subgroup contains atypical SDRs, some of which are identified as putative NAD(P)-dependent epimerases, one as a putative NAD-dependent epimerase/dehydratase. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine-rich NAD(P)-binding motif that is very similar to the extended SDRs, GXXGXXG, and binds NADP. Generally, this subgroup has poor conservation of the active site tetrad; however, individual sequences do contain matches to the YXXXK active site motif, the upstream Ser, and there is a highly conserved Asp in place of the usual active site Asn throughout the subgroup. 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. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. 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. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, 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.	3.64123e-48
NZ_CP023445.1|WP_096490936.1|21167_23213_-|Stk1-family-PASTA-domain-containing-Ser/Thr-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	3.85572e-127
NZ_CP023445.1|WP_096490934.1|18999_20346_-|FAD-dependent-oxidoreductase	gnl|CDD|215457	PLN02852, PLN02852, ferredoxin-NADP+ reductase.	1.9624e-135
NZ_CP023445.1|WP_096497529.1|18013_18793_+|class-E-sortase	gnl|CDD|320679	cd05830, Sortase_E, Sortase domain found in the class E family of sortases. Class E sortases are membrane-bound cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Actinobacteria). Genes encoding class A and E sortases are never found in the same organism, and similar to class A sortases, the genes encoding class E sortases are not positioned adjacent to genes encoding potential protein substrates, suggesting a housekeeping sortase function of class E sortases in some high G + C Gram-positive bacteria. Similar to class A sortase, class E sortases are capable of anchoring a large number of functionally distinct surface proteins containing a cell wall sorting signal to an amino group located on the bacterial cell wall. They recognize an LAXTG sorting signal, instead of the canonical LPXTG motif processed by class A sortases. The prototypical class E sortase from Corynebacterium diphtheria (named Cd-SrtF) is a non-polymerization sortase that is not required for pilus polymerization, and proceeds to complete the assembly process by anchoring the polymer to the cell wall peptidoglycan. Moreover, in Streptomyces coelicolor, one or both of Staphylococcus aureus SrtA homologs may function as class E sortase responsible for the cell wall anchoring of the long chaplin proteins (ChpA-C) containing an LAXTG sorting signal, which presumably mediate aerial hyphae formation. The family also includes some class E sortase homologs from Gram-negative and Archaebacterial species, but the functions of these enzymes are unknown.	2.31598e-52
NZ_CP023445.1|WP_096497530.1|37925_39092_+|MFS-transporter	gnl|CDD|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.03901e-18
NZ_CP023445.1|WP_096490946.1|36528_37788_+|family-1-glycosylhydrolase	gnl|CDD|274539	TIGR03356, BGL, beta-galactosidase.	0
NZ_CP023445.1|WP_096490932.1|17104_17371_-|cell-division-protein-CrgA	gnl|CDD|178907	PRK00159, PRK00159, putative septation inhibitor protein; Reviewed.	3.89381e-47
NZ_CP023445.1|WP_096490939.1|26414_27878_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	gnl|CDD|223843	COG0772, FtsW, Bacterial cell division membrane protein [Cell division and chromosome partitioning].	3.21885e-90
NZ_CP023445.1|WP_096490943.1|33231_34509_-|FAD-binding-protein	gnl|CDD|130740	TIGR01679, bact_FAD_ox, FAD-linked oxidoreductase. This model represents a family of bacterial oxidoreductases with covalently linked FAD, closely related to two different eukaryotic oxidases, L-gulonolactone oxidase (EC 1.1.3.8) from rat and D-arabinono-1,4-lactone oxidase (EC 1.1.3.37) from Saccharomyces cerevisiae.	9.95632e-99
NZ_CP023445.1|WP_012782663.1|29302_29767_-|FHA-domain-containing-protein	gnl|CDD|224630	COG1716, COG1716, FOG: FHA domain [Signal transduction mechanisms].	5.03264e-24
NZ_CP023445.1|WP_096490938.1|24951_26418_-|penicillin-binding-protein	gnl|CDD|274573	TIGR03423, pbp2_mrdA, penicillin-binding protein 2. Members of this protein family are penicillin-binding protein 2 (PBP-2), a protein whose gene (designated pbpA or mrdA) generally is found next to the gene for RodA, a protein required for rod (bacillus) shape in many bacteria. PBP-2 acts as a transpeptidase for cell elongation (hence, rod-shape). [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	6.3832e-94

Protein sequences

>NZ_CP023445.1|WP_012782663.1|29302_29767_-|FHA-domain-containing-protein
MPELVMQLTRAGFLILLWLFVLAALRVVRSDLYAASGLRVPTPSIKKGFRGAGKGGAKAPRQLVVTQGALSGTRITLDGKPIMIGRADDSTLVLDDDFASTRHARLSARGDEWFVEDLGSTNGTYLDRAKVTSPVRVPIGSQIRIGKTVIELRS
>NZ_CP023445.1|WP_096490940.1|27881_29306_-|serine/threonine-protein-phosphatase
MTLVLRYAARSDRGLVRQNNQDSVYAGPRLLALADGMGGHAAGEVASKVVIAALAPLDDDEPGDDLLGQLRDAVINGNGAISELVQSDPDLDGMGTTLTAVLFAGTRLGMVHIGDSRAYMMRNGTFSQITHDDTFVQSLIDEGRITEEEAATHPQRSLLLRALTGHEVEPRLMVREARPGDRYLLCSDGLSGVVTLETLDEAIRIPDPQACADRMIELALKGGGPDNVTVVVADVVDVDFGENAPIVGGAAGDGGDDPPPPDSPASRASSITGPRPAPPRQEQPPPPQQDPKRKRKGKLKALALVVLVLALLAAAGLGTRWWVMRQYYVGASQDGQVSVFRGVTGSVLGFELNTVVEGSCPPGSQGCEPISLDDLKVFMRDEVSSGITAVDGLEGAREAIRRLRTEQLLPLCADPLTSTPAPPTTTTGSATSAEQPPPSGDQDPSSSAPPTTTTEGTPLPTLAQTPGTDCRKGQ
>NZ_CP023445.1|WP_096490939.1|26414_27878_-|FtsW/RodA/SpoVE-family-cell-cycle-protein
MGSPGTGAGDTPLARASGTSPGLKPPPTKRSTELFLLAFGAVLVTAALVLVEANQEKELSLNIIWYGLAYLVMLAVTHLAVRTWAPYADPVILPCVTLLNGIGLVMIHRIDLGMADVVVDGEAWSAAAPKQVMWTGLSLVLFCAALKLLKDHRTLAKFGYVSGLIGLVALILPGVLPGFIAPTINGAKIWLRFGGVSIQPGEFAKILLMVFFAAFLVSKRDLFTIAGRRFLGMDLPRARDLGPLIAVWAVVVSVMVLQKDLGSSLLFFGIVLVLLYVATERAVWIIIGTALFMGAAVAAWRMFTHVQTRVDNWVDPFADPSGAGYQIVQSLFGFGTGGLFGAGLGGGRPDQIPEANTDFIAAVIGEELGLVGLTAVLLLYTVFALRGLRNALAVRDTFGKLLGGGLAFAVAFQVFIIIGGVMKLIPMTGITAPFLSKGGSSLLANYVLVALLLRISDAARSPQAPVKPRVQQPAIADQFTVMVERPK
>NZ_CP023445.1|WP_096490938.1|24951_26418_-|penicillin-binding-protein
MNTPLRRVGVAMMVMMMILLANATYVQVIKAEEYRTNAYNVRGRLEMLSRERGSIIAADGTPLATVTPIPDKDRWQRVYANGPMYLPVTGYLSNTYGSNGLERAENDLLIGEDDRLFTRRLSDLITGRDPKGASLQVTINPKAQQAAYEALGDRTGAVVAIEPKTGKILALVSTPSFDPNKLAVQDGEEEKAYWAEVTQDNAAQPDANRALSWTYPPGSTFKLVVAAAGLEEGMDKSTQVDARPTITLPGTNTELPNFNGNNCNNGVNATLEQAIAESCNTAFAKLAGDLGTAKLREQAAKFGIDDQKFQVPMTTAASTIGPIPDQAALFQTGIGQRDVQVTPLANAVMVATIANKGVRMKPYLVDKILGTDTATVDETKPDEVEEAMSEDSAQLLTEMMIAAENKAGGTGKLSNIQIASKTGTAEWGAGSTPNPHAWYTAFAPANDPQIALAVIVEKSGGQSGGNATGGRVAAPIGRAVISSYLGSR
>NZ_CP023445.1|WP_096490937.1|23293_24952_-|serine/threonine-protein-kinase
MLSSGQLLAERYRLTRRIAVGGMGEVWEAADTRLDRNVAVKVLKAELSGDAEFLNRFRIEARTTASLNHPGIAGVHDYGETASEPDGPEDTAYLVMELVEGEPLAAIIARGRMNAERVLDVLEQAGTALQAAHERGLVHRDVKPGNILVTPDGKVKITDFGIAKAADAAPVTRSGMVMGTAHYIAPEQATGHDAEPASDVYALAVCGYECLVGHRPFRSENAVTVAMMHIRDVAPPLPPDVPPAVRALIEATLVKDPRQRYRNGGEFASAVAAVRAGQPLPAPSGLAMAVGGPQLAPPPQAPPSQQLPVQQLQAQPMQAQPVQAQSMQVQPLQAQPMSAPPMPQQPMPSQQLPAQLAPPQQLAAPPPMAPQQLTPPAQLTHPGIPVTHPGSRPGMQPIHPPAAGPHTGAFHPPGAPGRHPGRGRPLLWVMVAFLVIALIALSVLIVREIAGDDGVPGGPSPQGSTPSASRAAPEDATDRFPGRPTVEITGADYLGAPADEVAATLTGHGVEPEVRSERGGAPADARRCRVSELEPEGEVPIGSRVRVTCVPT
>NZ_CP023445.1|WP_096490936.1|21167_23213_-|Stk1-family-PASTA-domain-containing-Ser/Thr-kinase
MSTPRLLSNRYELGETLGYGGMSEVHKGKDVRLSRDVAIKVLRADLARDAQFQERFRREAQNSAALNHPAIVAVYDTGETETQYGPLPYIVMEYVDGRTLRDIVKTQGPLSNKRAMEVMADVSAALDFSHRHGIVHRDVKPANVMITRSGAVKVMDFGIARAVHDGQAAVTQTAAVIGTAQYLSPEQAKGEAVDGRSDVYASGCVLFELLTGEPPFTGDSPVAVAYQHVREEPKSPSSLNPKVSPALDSIVLKAMAKGPANRYQSAAELRADLVRVLSGQRPSAPVVMTSEERTALLDQQSPSAPARTEAVQTTSGGGRHRQSAVRERERERDREDTGNYSAALEEERERLAARRRMWMITIVALLCAGVLALAIWITTSLLGSTESSGGDPKQVTVPTLVGKSSSEARSALSDAGLEINLQLVPCQPGSQPKCDPAKDVDRVLETSPASGKSVDRNSKITVMVGTNPDDIEVPDLTGLSVADAQAKLGEDWKLDTNQERVETSDPAKVDKVVEQNPMHGTKAPKGTTITIKIGKEPEAVTLSNVIGVQEDDARASLEQSGFKVQVKQVDSATDAGQVIAQDPGAGRVEKGSTVTLSVSKGNMVSMPDLRGMTETEAKAALRLLQWNGDLQTSKTPVSDLSQDRKVQSQQTSPGSAITKAQRITVVVGEFRPGASSAPPSN
>NZ_CP023445.1|WP_096490935.1|20411_21053_+|aminodeoxychorismate/anthranilate-synthase-component-II
MRVLVVDNYDSFVYNLVQYLAQLGAECVVKRNDEVEPADVAAAGGVLVSPGPSTPHRAGRSMDVVRWCVDSGVPVFGVCLGHQAIGAVWGATVDLAPELLHGKTSVVHHEGAGVLAGLPRPFTATRYHSLTVLPETIPDEFEVTCRTEGGVVMGMRHRELPVEGVQFHPESVLTDGGHRMLANWLAVCGYEVPEAVVGGLERNMRDLAAAARR
>NZ_CP023445.1|WP_096490934.1|18999_20346_-|FAD-dependent-oxidoreductase
MSRSLRVAVVGAGPAGIYAADILTKSDAEVSIDLFERMPAPYGLIRYGVAPDHPRIKGIVNALQKVLDRPEIRFFGNVEYGVDVKLEDLRQHYDAVIFSTGAEKDRALDVPGIELDGSYGAADFVSWYDGHPDVPRTWPLTASQVAVLGVGNVALDVARVLAKTADELLTTEIPDNVYEGLKSSPVTDVHVFGRRGPAQAKFTPLELRELDHSPNVEVIVHPEGIDFDEGSMASIRSSKQVEMVVKTLQEWALRDVGDRPRRLHLHFLEAPVEVTGEDGKVVGLRTERMELTGDGNVRGTGEFTDWPVQAVYRAVGYLSTSLVDLPFDTASGTVPHAGGRVVDLDEQPLPGVYVTGWIKRGPVGLIGHTKGDALETVTNLLADADALPACQFPEPDAIVRFLEQRAVPFTTVEGWLKLDAHEKALGAERGRERVKVVDRETMTSVSRS
>NZ_CP023445.1|WP_096497529.1|18013_18793_+|class-E-sortase
MRKVVRGTGEALITLGLVVLLFVVYEVYVTDLISAGKQDDVTSALDEEWKDSNTVAADPQREVKYDLLDGKAFAKIYIPVFGADYKFSIVEGTTDKDLETGPGHYKGTALPGEKGNFAVAGHRVGKGSPFNDLDLLNSCDAIVVETQASWFVYRMLPKNSEVAGWASRASDPRCKDVGPLSGPYSKTQGQEIVLPSAGEVINEVPYNEAQVPEDQLKSLMTLTTCHPRFSDKQRLIVHATLAQHYPKSDGFLPPELKEQ
>NZ_CP023445.1|WP_096490932.1|17104_17371_-|cell-division-protein-CrgA
MPKSKVRKKAVYTAPADRRTPVKVKAAGPSHPFYITVMLGVMLLGLAWLVVNYIAGEKIPVMMDLGSWNFGIGFALIIVGLLMTMRWR
>NZ_CP023445.1|WP_012782665.1|31712_32333_+|hypothetical-protein
MSSTPARIEVTDSAKAKATSAAAVPIPELPGSVEELATVAAVRLGWHGVVLPEMVLMGRKVVVVADLIADAHAERLCLGAAPEVDRATVSTWVWPEMDGRVPPAAVRIVGVLAVARHWRTALASAVPFARFGNAAAVLPASVALSHDYLANCLPRVRRYGVNVLLADESSELTTDVCGRNETVPVEDTATTRWVNELVYERVLATA
>NZ_CP023445.1|WP_096490942.1|32383_33019_+|SDR-family-oxidoreductase
MRLVIAGGHGKIALHVQRLLAAGGDAATALVRNEDHFADVTEAGGVPVLCDLEASDVASVAEYLTGADAVLFAAGAGPGSGVGRKDSVDRGASALLADAAERAGVRRFVQISSAGIGRTTGDEVFDAYLLAKGAAEEDLKARDLDWTIVRPGRLTDEPATGAVRLTEGDARDGAVPRADVAAVVVALLGRPSSVGKTYELISGETPVQDAI
>NZ_CP023445.1|WP_096490943.1|33231_34509_-|FAD-binding-protein
MAPPWTNWARTETAAPIRVEHPTTAEGISEVVRTADAVRARGSGHSFTGVAVAPSVALDLDRWTGLVDVAGELVTVRAGTTLRQLNELLHREGLAMPNLGDIDAQTIAGATSTGTHGTGAALGGLATTIAALEVVLADGSLVRCSPAERPELFEAARLGLGAVGVISTLTLRCVPSFVLHAREYPARLDAVLEEFDHLTATEDHVEFHWFPHGDRVIVKRNNRVDEPCAPLSGLRRFYEYDVMENAAFGAVCKVARAVPAAARGLNRVCGALIGERDYRDQSHRVFTTPRRVRFVETEYAVPRAELHGVLRELRAAVAGLEHGVIVPVEVRVARGDDIWLSTAHGRDTAYVAVHQYVGMPHRRYFDAFERIALAVGGRPHWGKMHSLGAEELATRYPRFADFRRVRAEVDPDRKFGNRHLERVLG
>NZ_CP023445.1|WP_096490944.1|34592_35780_+|amino-acid-deaminase/aldolase
MQPRTRLDLATKDLEAPLAIVDLDAFDHNAADLVRRAGGKPIRVASKSVRVRALLDRVLARPGYAGLMCYSLPEALWLSSCDTAEDLLVAYPTVDHAALRALAADEKARRRVTIMVDSTAHLDLVDAALGEDHPEIRVCLELDVSWRPLPGVHVGPRRSPVHTEGDAVRLARAVVARKGFRLVGVMAYEGQVAGIGDAPAGRRAWGLAVRWMQGRSVPELTERRAAAVAAVRRVADLEFVNGGGTGSLETTGADRSVTELAAGSGLVGPTLFDAYRAFSPRPAALFALPVVRRPKKNVATLFAGGYVASGTGTPDRLPSPHLPSGLELIGLEGAGEVQTPVVGRAADRLELGDRVWLRHAKAGELAERFAEYHLVSGDRVEAVVPTYRGEGKAFG
>NZ_CP023445.1|WP_096490945.1|35776_36442_-|TetR/AcrR-family-transcriptional-regulator
MKAPTSPAGVAVTSTTPLRRQPVQQRSAKRVERMLEACAALIEEVGYDGVTTTLIAERAGVAVGSLYQFFPDKRAVVQELTLRNLERFIQTVDGTFTTKALAHWWDAVDSIFDVYVTMHREVPAFSRLHFGDVVDLRLMDDRKDNNSVVSDRIAEMISSRFSIPLDEVKLPISIAVEAADGVLGLAFRRDPAGDPLVLDEAKAMIRGYLSTRMPGQPPATA
>NZ_CP023445.1|WP_096490946.1|36528_37788_+|family-1-glycosylhydrolase
MTGPDFLWGVSTSAFQIEGGFDEDGRLPSVWDEFPSFEGQTARVACDHRNRHAEDVALLRELGVNAYRFSLSWPRVEGGRAARGGSAGGGLDFYDRLVDDLLDAGIAPVATLYHWDTPAHVEEAGGWLARDTAHRLADYAATAAARLADRVAMWIPVNEPAMVTLLGYATGQHAPGKALLFDALPTAHHLNLGHGLAVQALRAAGATSVGTANNHTPAWAATGSAEDAAAASAYADLHNWLYADPVLAGRYPDSLVDLLPVEDGDLATIAQPLDFYGVNYYNPTRLSAPSPGNPLPFDLVPITEHPVTGFGWPVVPAGLGEMIDALRARHPDLPPVLVTESGCSYPHSLDDTERVDYLAAHSEAAIAAGAKGYFVWSVLDNFEWDSGYSQRFGLVHVDYATQRRTPRASFRWYRDRIRR
>NZ_CP023445.1|WP_096497530.1|37925_39092_+|MFS-transporter
MLFLANLGLWLGVYAPIQVLLPQQAERISPDAKELVFGLVTALGAAVALIANPLIGLSSDRTCSRFGRRHPWTLAGALVGALGLAVLSAADATWSMALGWCLVQAGLNGMLASLTSGVPDRVPVAQRARVGGLVGISQMLGTVLGAVVVTVLVTGQTAGYLVCAALVVAGALAFVLATPDARLPRAARPPLVARELWVSPKRHPDFAWAWTAHFAINLGNALGTLYLLFFLADEVRHPSPEDGLLVLMLLYGAALVVGAVLVGARSDRTGRRRGGVHLSAALMALAALLLAAWPTWWSALIAAPLLGFGFGAYWAVALALLTQVLPAATDRAKDLGVVNVANALPQVLAPALASVVLVDLGGYRGLFLLSAAATLVASLCVTRIRGVR
>NZ_CP023445.1|WP_096490947.1|39088_39856_+|SDR-family-NAD(P)-dependent-oxidoreductase
MRVLVTGASQGIGAAVAERFAAEGAEVHLVARGAVALAAVVERITARGGWAVAHVADLADERLVLALAEEVGPVDVLVNNAGIGRWLFLDDTAPDELRGMTALPYSSYALLTSLLLPAMRERGSGRLVFLNSPASRIAIPGATGYTAARWAVRGLVAALRQDLRGTGVGVTEVVPGAVRSNYFDNNPGSAERIPRVVSRLVPTLTPERVAAEVVKAVARGRSEVVFPWQIKLFDLVGRVIPGAVAYLAWRTGVHR
>NZ_CP023445.1|WP_012782673.1|40228_40591_-|hypothetical-protein
MDEILGQVLRNAVWERLDLLTELASQADAPSLLSVARSELPRLTEGWRALLAAHEPDDKGNCPECSGRWRQQKSPCSVWRAAYEHLVAGGLAPRPARHLRTAPVTPPVTRSRRGVAVRAH
>NZ_CP023445.1|WP_096490948.1|40604_40928_-|hypothetical-protein
MDLIEQAVTTRRGGVAGEVVLGVSPSTSLSIQEPTDLGSGWRGSTGQRRRWCSSPDGVDGRDRSSTARTSGGPAPLVGPTGGAAVLSADRLVQLRAALREAAEKAER

Crispr_ID: NZ_CP023445_2

• CRISPR_ID: NZ_CP023445_2
• CRISPR_location: 892043-892135
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_2

Consensus_repeat	Method
GGCGGTCGCCCCGGTGACCCCCGCGTCC	CRISPRCasFinder

spacers of NZ_CP023445_2

>2.1|892071|37|NZ_CP023445|CRISPRCasFinder
CGCCCCCGAAGCTCCCCACCTCCCGGACCCCCGACCG

CRISPR arrays and Neighbor proteins around NZ_CP023445_2

CRISPR arrays

The CRISPR arrays of NZ_CP023445_2

>merge|NZ_CP023445|2|892043-892135|CRISPRCasFinder
GGCGGTCGCCCCGGTGACCCCCGCGTCCCGCCCCCGAAGCTCCCCACCTCCCGGACCCCCGACCGGCGGTCGCCCCCGGTGACCCCCGCGTCC

>NZ_CP023445|2|1|892043-892135|CRISPRCasFinder
GGCGGTCGCCCCGGTGACCCCCGCGTCC	CGCCCCCGAAGCTCCCCACCTCCCGGACCCCCGACCG
GCGGTCGCCCCCGGTGACCCCCGCGTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096491570.1|883509_884544_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|184875
NZ_CP023445.1|WP_096491578.1|898066_898792_+|cobalamin-biosynthesis-protein-CbiX	unknown	unknown	gnl|CDD|225049
NZ_CP023445.1|WP_096491571.1|884614_885649_+|DUF3152-domain-containing-protein	unknown	unknown	gnl|CDD|371483
NZ_CP023445.1|WP_096491567.1|880482_880827_-|DUF4873-domain-containing-protein	unknown	unknown	gnl|CDD|374407
NZ_CP023445.1|WP_096491574.1|890582_892019_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224171
NZ_CP023445.1|WP_096497607.1|896972_898070_+|uroporphyrinogen-III-synthase	unknown	unknown	gnl|CDD|235981
NZ_CP023445.1|WP_096491572.1|885783_886956_+|adenylyltransferase/sulfurtransferase-MoeZ	unknown	unknown	gnl|CDD|181156
NZ_CP023445.1|WP_096491581.1|901811_902135_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096491568.1|880823_881639_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP023445.1|WP_096491579.1|899164_899617_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096491580.1|899741_900419_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP023445.1|WP_096491576.1|894007_896512_+|nitrite-reductase-large-subunit	unknown	unknown	gnl|CDD|184951
NZ_CP023445.1|WP_096491583.1|903308_904748_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349929
NZ_CP023445.1|WP_096491573.1|888406_890440_+|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl|CDD|239155
NZ_CP023445.1|WP_096491577.1|896508_896847_+|nitrite-reductase-small-subunit-NirD	unknown	unknown	gnl|CDD|239605
NZ_CP023445.1|WP_096491575.1|892260_893613_+|NarK/NasA-family-nitrate-transporter	unknown	unknown	gnl|CDD|225133
NZ_CP023445.1|WP_096491582.1|902229_903309_-|potassium-channel-family-protein	unknown	unknown	gnl|CDD|367001
NZ_CP023445.1|WP_118945366.1|887476_888274_+|TIGR02569-family-protein	unknown	unknown	gnl|CDD|131620
NZ_CP023445.1|WP_096491569.1|881700_882600_+|diiron-oxygenase	unknown	unknown	gnl|CDD|378680
NZ_CP023445.1|WP_096497606.1|882753_883398_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096491570.1|883509_884544_+|alpha/beta-hydrolase	gnl|CDD|184875	PRK14875, PRK14875, acetoin dehydrogenase E2 subunit dihydrolipoyllysine-residue acetyltransferase; Provisional.	2.10922e-27
NZ_CP023445.1|WP_096491578.1|898066_898792_+|cobalamin-biosynthesis-protein-CbiX	gnl|CDD|225049	COG2138, COG2138, Sirohydrochlorin ferrochelatase [Inorganic ion transport and metabolism].	2.3174e-18
NZ_CP023445.1|WP_096491571.1|884614_885649_+|DUF3152-domain-containing-protein	gnl|CDD|371483	pfam11350, DUF3152, Protein of unknown function (DUF3152). Some members in this family of proteins are annotated as membrane proteins however this cannot be confirmed. Currently there is no known function.	9.47234e-81
NZ_CP023445.1|WP_096491567.1|880482_880827_-|DUF4873-domain-containing-protein	gnl|CDD|374407	pfam16170, DUF4873, Domain of unknown function (DUF4873). This family consists mostly of short uncharacterized proteins found in various high GC Gram positive bacteria, primarily Mycobacterium species. However in some proteins, such as for instance Rv0943c proteins from Mycobacterium tuberculosis H37Rv, DUF4873 domain is found at the C-terminus, following the flavin-binding monooxygenase-like domain pfam00743, which is why probably many proteins with DUF4873 domains are annotated as monooxygenases. However these functions are not confirmed experimentally and the function of DUF4873 domain is still unknown.	7.22704e-41
NZ_CP023445.1|WP_096491574.1|890582_892019_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224171	COG1251, NirB, NAD(P)H-nitrite reductase [Energy production and conversion].	1.06097e-137
NZ_CP023445.1|WP_096497607.1|896972_898070_+|uroporphyrinogen-III-synthase	gnl|CDD|235981	PRK07239, PRK07239, bifunctional uroporphyrinogen-III synthetase/response regulator domain protein; Validated.	9.75354e-162
NZ_CP023445.1|WP_096491572.1|885783_886956_+|adenylyltransferase/sulfurtransferase-MoeZ	gnl|CDD|181156	PRK07878, PRK07878, molybdopterin biosynthesis-like protein MoeZ; Validated.	0
NZ_CP023445.1|WP_096491568.1|880823_881639_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	8.07727e-13
NZ_CP023445.1|WP_096491580.1|899741_900419_+|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].	3.39932e-68
NZ_CP023445.1|WP_096491576.1|894007_896512_+|nitrite-reductase-large-subunit	gnl|CDD|184951	PRK14989, PRK14989, nitrite reductase subunit NirD; Provisional.	0
NZ_CP023445.1|WP_096491583.1|903308_904748_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349929	cd05680, M20_dipept_like, uncharacterized M20 dipeptidase. Peptidase M20 family, unknown dipeptidase-like subfamily (inferred by homology to be dipeptidases). M20 dipeptidases include a large variety of bacterial enzymes including cytosolic nonspecific dipeptidase (CNDP), Xaa-methyl-His dipeptidase (anserinase),and canosinase. These dipeptidases have been shown to act on a wide range of dipeptides, but not larger peptides. For example, anserinase mainly catalyzes the hydrolysis of N-alpha-acetylhistidine while carnosinase degrades beta-alanyl-L-histidine.	5.41784e-172
NZ_CP023445.1|WP_096491573.1|888406_890440_+|molybdopterin-oxidoreductase-family-protein	gnl|CDD|239155	cd02754, MopB_Nitrate-R-NapA-like, Nitrate reductases, NapA (Nitrate-R-NapA), NasA, and NarB catalyze the reduction of nitrate to nitrite. Monomeric Nas is located in the cytoplasm and participates in nitrogen assimilation. Dimeric Nap is located in the periplasm and is coupled to quinol oxidation via a membrane-anchored tetraheme cytochrome. Members of the MopB_Nitrate-R-NapA CD belong to the molybdopterin_binding (MopB) superfamily of proteins.	0
NZ_CP023445.1|WP_096491577.1|896508_896847_+|nitrite-reductase-small-subunit-NirD	gnl|CDD|239605	cd03529, Rieske_NirD, Assimilatory nitrite reductase (NirD) family, Rieske domain; Assimilatory nitrate and nitrite reductases convert nitrate through nitrite to ammonium. Members include bacterial and fungal proteins. The bacterial NirD contains a single Rieske domain while fungal proteins have a C-terminal Rieske domain in addition to several other domains. The fungal NirD is involved in nutrient acquisition, functioning at the soil/fungus interface to control nutrient exchange between the fungus and the host plant. The Rieske domain is a [2Fe-2S] cluster binding domain involved in electron transfer. The Rieske [2Fe-2S] cluster is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In this family, only a few members contain these residues. Other members may have lost the ability to bind the Rieske [2Fe-2S] cluster.	9.09045e-47
NZ_CP023445.1|WP_096491575.1|892260_893613_+|NarK/NasA-family-nitrate-transporter	gnl|CDD|225133	COG2223, NarK, Nitrate/nitrite transporter [Inorganic ion transport and metabolism].	6.88077e-104
NZ_CP023445.1|WP_096491582.1|902229_903309_-|potassium-channel-family-protein	gnl|CDD|367001	pfam02254, TrkA_N, TrkA-N domain. This domain is found in a wide variety of proteins. These protein include potassium channels, phosphoesterases, and various other transporters. This domain binds to NAD.	1.29761e-20
NZ_CP023445.1|WP_118945366.1|887476_888274_+|TIGR02569-family-protein	gnl|CDD|131620	TIGR02569, conserved_hypothetical_protein, TIGR02569 family protein. This protein family is found, so far, only in Actinobacteria, including as least five species of Mycobacterium, three of Corynebacterium, and Nocardia farcinica, always in a single copy per genome. The function is unknown. [Hypothetical proteins, Conserved].	2.9401e-78
NZ_CP023445.1|WP_096491569.1|881700_882600_+|diiron-oxygenase	gnl|CDD|378680	pfam11583, AurF, P-aminobenzoate N-oxygenase AurF. This family is a metalloenzyme which is involved in the biosynthesis of antibiotic aureothin by catalyzing the formation of p-nitrobenzoic acid from p-aminobenzoic acid. AurF is a non-heme di-iron monooxygenase which creates nitroarenes via the sequential oxidation of aminoarenes.	2.77099e-118
NZ_CP023445.1|WP_096497606.1|882753_883398_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.78858e-16

Protein sequences

>NZ_CP023445.1|WP_096491574.1|890582_892019_+|NAD(P)/FAD-dependent-oxidoreductase
MRRVVVVGHGMAGARFAEEVLRRDPGGERVGLTLLGAERHPAYNRVLLSSVVAGALPPESVRLHAPDWAERSAVDLRLGASVGKVDRVRRVVQVDDGEVPYDALVLATGARPWLPPVAGLTGVDGVLAPGAVAFRTLDDCAAITSAARPGAPVVVLGGGLLGLEAARGLVARGCLVTVVHPRSHLMERQLDAGAGRVLARALGGLGVELRLGAVAERYEPGEGLLLADGTRLAADLLVVAAGVRPSVELAAQAGIAVDRGVLVDDALRTDDPRVHAIGDCAQHEGAPTGLVQPAWEQAVVLADRLTGTDPAARYRGGGAVTRLKARDVDLVALGEAHVGVDDERAEVLALEDPARGRYAKLVLRDDRVAGAILLGVPDAAAAVTQLYDRGLPAPSDRLGLLLGRALPAGAVAEASPADLPAGAVVCRCNTVSKGQLVSAWRAGARSVPGLVEATRASTGCGGCRDAVCGIADWLAAAE
>NZ_CP023445.1|WP_096491573.1|888406_890440_+|molybdopterin-oxidoreductase-family-protein
MTDTHCPYCALQCAMTIVDGEVSPREFPTNRGGLCQKGWTSAALLTSPARLTTPLVRDRTPEGARGELRPASWDEALDLVAARLAALRRDHGPDSVGVFGGGGLTNEKSYLLGKFARVALGTSQIDYNGRFCMSSAAAAGTRAFGLDRGMPFPVTDLDDSNAVLLAGGNPAETMPPFVQHLRGAALVVVDPRRTATAELAAVHLAPAPGTDLALALGLLHVAVADGHLDKTYVAERTTGFDDAWRIAATWWPERVERVTGVPVADQRAAVRLLAEADRAHVLTGRGTEQHASGADAVSAWINLALALGLPGTPGSGYGCLTGQGNGQGGREHGQKADQLPGYRKITDPAAREHVQRVWGVDGLPGPGRSAYELLDALGGPDGPKALLVFGSNVVVSAPRAGHVADRLAALDLLVVADLVLSETAAVADVVLPVTQWAEESGTMTNLEGRVLLRQRAVRAPDGVRSDLEVLRGLAERLGQPGERFPVEPEVVFEELRRASAGGLADYSGVTYSRLAAGEALHWPVVPDSTPRVFLDRFAHPDGLARFAAVDHRGPAEPPDADYPLQATTGRVLQHYQSGAQTRLVAELVAAEPEAYVEVHPDTAGRAGLAHGGMAAVVSRRGRTVARVRCVASMRVDLVFLPFHFPGDGRANLLTNPALDPVSRMPEFKVCAVRLERV
>NZ_CP023445.1|WP_118945366.1|887476_888274_+|TIGR02569-family-protein
MTPTPEPPPSHVRAAFGARDVEPELIDGGPAWRCGEAAIRPAGKPAEATWVAKTLDALDVEGLRVARPLRSTDGRYVVGGWAATKYLSGRAEPRHDDVVEVAVRLHEATAGMTKPRFLDARTDLFAVADRCAWDDERTALRPELGGRLFELMTSYRKPITAKPQVVHGDLFGNVLFAGDAPPAIIDFAAYWRPAPYGAAVVVVDALSWGGADRGLVQRWSHLEEWPQVLLRALLFRLAVHALHPQSSARSLVGLERAAGTVVELL
>NZ_CP023445.1|WP_096491572.1|885783_886956_+|adenylyltransferase/sulfurtransferase-MoeZ
MALPPLVEPAAELTKEEVARYSRHLIIPDVGVDGQKRLKNAKVLVVGAGGLGSPALLYLAAAGVGTLGVVDFDVVDESNLQRQVIHGQSDIGKPKAESARESVAEINPFVKVVLHQAQLTSENALEVFRDYDLILDGTDNFATRYLVNDAAVLLGKPYVWGSIFRFEGQVSVFWEDAPNGQGLNYRDLYPEPPPPGMVPSCAEGGVLGVLCASIGSIMVTEAIKLLTGIGDPLLGRLMVYDALEMSYRTIRIRKDPESPKITELIDYEAFCGVVSDEAQQAAAGRTITPLELKQKQDAGDDFVLIDVREPHEYEIVRIPGSVLIPKDRILSGEALAELPQDKPIVLHCKSGARSAEALAALHRAGFADAVHVGGGVLAWARQIDQSLPTY
>NZ_CP023445.1|WP_096491571.1|884614_885649_+|DUF3152-domain-containing-protein
MNRTSGQRRGPAPSPAPARSALTEDRYRRGARRTAGEPLAASWEPDGAKPRERKRSIKNLIGNYGWRIYAVPVLVVLTALVVLDTAAQDDQGGGVAQQGGGLGQDRSEQAEDHPKVDETPPANTALVDIPTAVLPEGPSYTEQGAGTWEVVQGRTEKVGDGPLRKYAIEIEVGINPIDHGGDVTTFARTVDAYLADQRSWVGTGNVSMQRVDDGSEDFRISLTSVQTTHGLCGNQIQYESSCYNPDREKVVINVSRWVRGAKAFSNDIANYRQYAINHEVGHALGKGHEACKDDGRPAPVMMQQTFGVANDYVAKLNEVDASNRGAVPADGKTCTPNAFPVAPQ
>NZ_CP023445.1|WP_096491570.1|883509_884544_+|alpha/beta-hydrolase
MTFPRAARFTLPRRRHPGGVTQPQEATRTALTRVPLSTAALPPLDTAIPPWPGEQVQVDGHRLHVRTTPGPEGADTAVYVHGLGGSSTNWTDLSGQLAGHVEGRSVDLPGFGRSEPVDGYTYSIAAHARAVTRYLESLGRPVHLFGNSMGGTISLVIAATRPELVKSLVLVSPAMPDLRLSTSRMADPLIALAYLPLVGRTARKRLAQVSHEERARQTVRLCFSDPSIVPDNRIAESGREVAERATQAWASAALGRSTTELVRSWLLRGPSSLWLLPPEVTAPTLVVWGADDRLVSVRKAPRLTRSLPRGRMLVLPRTGHVAQMERPVLVARAVAGMWEAGDRW
>NZ_CP023445.1|WP_096497606.1|882753_883398_-|TetR/AcrR-family-transcriptional-regulator
MTETAQTVGQNGGSAGRGMRLPRTARRAQLLAAAQDVFVSNGYHAAAMDEIAERAGVSKPVLYQHFPGKLELYMALLESHVDGLVARVRGAIESTTDNKQRVRAAVAAFYDFVDDQGQAFRMVFESDLRGEPAVASAVERATADSVDAITETITSDAGLDEHRARLLATGLVGLSQVTARSWLAGDRAIPKEDAVTLISNLAWKGIGGGFPLQH
>NZ_CP023445.1|WP_096491569.1|881700_882600_+|diiron-oxygenase
MARQLKATDREKTAERLLNSSAARSYDPEVDVDWSAPLVDGLLYLPEHRTSLYGTELWAGLSREQRVELGRHEVASVASVGLWFEVLLMQLLLKDVYSGDPTSRHVQYALTEIGDETRHSTMFARMVERIGCPAYGPGRRVHRLGRLLPVIGRGPAVYAAILVAEEVLDRLQREMTADEGVQPLVRMVSRIHVLEEARHVRFAREEVVRGVRGLSRAELPYQRWLLAVVAMHITRSLIHPEVYRAVGLDPVEAARAAAGNPQWRETIRWAGERVVAFLDEVGLVGAPGGHAWRRSFLVG
>NZ_CP023445.1|WP_096491568.1|880823_881639_-|TetR/AcrR-family-transcriptional-regulator
MVRTVKGGTDARRERWKGHREARRAEFVEATIRAVARHGADVGMDEIAGEAGVSKPVLYRHFADKADLYLAVGRRATELLMDRLGPAIEGDGSLRARITRIVDAYLSVIEEHPHLYRFVVRAAFAERPVEQDVVGEDKAMIATALTRLFGDFLRANGMDSGGAEPWAHALVGMVQNAGDWWLDRQSMSRASLGDYLSTIIWHALDGLLRSAGVVLDPDEPIEARVSGASGQAGRAGAGQAPVGSGRAGAAQGGAAQAGQAQAGLRLVGEQP
>NZ_CP023445.1|WP_096491567.1|880482_880827_-|DUF4873-domain-containing-protein
MTGAGAGPEPAPDGQPEGQFEDHEGYSGPAVLLLGGHEVPVEVDLRGFFQPIDGRYHWYGRIAADPRVTGLVEAGARTADLRTPAGSATGSLGDPDPWGRYRVAGTGAPPFPTA
>NZ_CP023445.1|WP_096491575.1|892260_893613_+|NarK/NasA-family-nitrate-transporter
MSTVHEDRGAVARSRRGGRWIDRWEPEDPEFWAREGRRVARKNLVFSVLAENLGFTVWSLMSIVVVSLGQVGFAFTVGQTFWLLIVPNLVGAVLRVPYTFAVPRFGGRAWTAFSAGMLLIPCAMLAHAVSTPGTPYWFFLLTAATTGFGGGNFSSSMANISFFYPEGKKGLALGLNAAGGNLGVAMVQLVVPIVITWGTGINLAHAALVWMPFVVVSTACAWLFMDSLTEARPDGTSYRLAMTNRHTWVMSLLYIGTFGSFIGFSFAFPSLIKLSFAEQKGFVALAFLGALIGSVTRPFGGWLADRLGGARVTVGVFVGLALGCAGVLVSVEARSFPLFFGSFIVLFVLTGLGNGSTYRMIPAIFATQVADAASAKRQAAAVVGIAGAVGAFGGVLVNLVFKFSLEGGKTLAPALTAFLGFYALCVVTTWWFYLRRVSFGRAPSLAHAGI
>NZ_CP023445.1|WP_096491576.1|894007_896512_+|nitrite-reductase-large-subunit
MTRTLLVVGHGMVGHRLVQAVRERDVDGAWRVVVLAEEPRAAYDRVALSSYVDTWDASGLALEPHDDAVELRLGESATGIDRAAKRVRTSTGAELAYDALVLATGSSPFVPPVPGRDLPGCHVYRTIDDLDAIRATVDAARHRGAGQRGMGRRAGMVLGGGLLGLEAANALRGMGISPHVVELGPRLMPLQIDEGGGALLGRMVEKLGLTVHTGVSATAVTRDGDRLAATLSDGRELDLDVVVFSAGIRPRDELARAAGLDVGPRGGVVVDGGCRTSDPDVYAVGECALVGGAVYGLVAPGYAMAEVVADRLLGGAAEFPGADTSTKLKLLGVDVASFGDAHATSPGALEVVVNDAVAGTYAKVVVSDDARTLLGGVLVGDASRYSALRPLVGRPVPGDPVSLIGAAAVEPALPADAQVCSCHAVTKQQVTDAITSGQAADVPGIKACTKAGTGCGSCVPMLKKLLAECGVEQSRALCEHFPQSRAELFEIVRSTGIGTFSELVARHGSGRGCDLCKPAVASILASLENGHILGGEQVTLQDTNDRFLANIQRNGTYSVVPRIPGGEITPEKLIVIGEVARDYGLYTKITGGQRIDLFGATVDQLPLIWRRLVDAGFESGHAYGKSLRTVKSCVGSTWCRFGVQDSVGLAIELELRYRGLRSPHKFKSAVSGCARECAEARGKDFGVIATENGWNLYVGGNGGFTPRHADLLVSDVDTETLVRIIDRFLMFYIRTADKLQRTAPWIESMEGGLDHLRDVVVHDSLGICADLEAAMAKHVDSYADEWRGVLDDPEKLARFTSFVNAPGAPDPTISFREERGQRVPVVLGIPEVAR
>NZ_CP023445.1|WP_096491577.1|896508_896847_+|nitrite-reductase-small-subunit-NirD
MTGVCPMTPVCELSALQPERGVAALLPDGTQVALFLTSDGGLHALGNVDPFSGAAVLSRGIVGDRGGVPVVISPLYKQAFELSTGRCLDDPAVVVESYPVSVVEGVVRVGAP
>NZ_CP023445.1|WP_096497607.1|896972_898070_+|uroporphyrinogen-III-synthase
MGVTAARRAEELVALLERKGAAVLHGPAIRIVPLHDDAKLLEATELVLARQVDAVVATTGIGFRGWVEAAEGWGLGARLLTALGDGLLLARGPKARGAVRAAGLVEDWSPSSESNAELLEHLLGLGVAGKRIAVQLHGIPLPEFTGALREAGAEVVEVPVYRWTGPADPGPLERLLEGVLSGQVDAMTFTSAPAAASVLETARQMGRYEEVVGALRRVLVVCVGAIAAGPLVAVGVPVVQPGRARMGALAREVVVELPARAVRVPVEGREIELRGQGVLVDGELRPVAPAPMAVLRALVQARGRVVSRKELLAALPGGGEEHAVETAVGRLRTALGDPGVVATVVKRGYRLAVEPSRFECGGVAV
>NZ_CP023445.1|WP_096491578.1|898066_898792_+|cobalamin-biosynthesis-protein-CbiX
MSAGGTLVLVAHGTRHPGGGVVVEEIARLVRERGGVDVRVAYADVRQPDVTAVLREVRGAAVVVPAFLAAGYHVRVDVPAQVVASGHRDVVITEPIGAAVVPAVVERLREAGWREGDPVVLGAAGSSDARALGEVRKVAEVLGQRVGGPVRVGYAATASPRIGEVVAEVRAAGVGAGVGGAGAGWGGRVAVASWLLAPGVFHRGMRECGAEIVSEPIGAHDRVVEAVLLRYYEGRCSRWAA
>NZ_CP023445.1|WP_096491579.1|899164_899617_-|hypothetical-protein
MALRLNPVRWALALLVVGLAAVAVVVALSWPESTAEGALTEATVTTPAPCSGPEAFDQVAYDLNGTRHEAKLDGCGHSENEIVRVLVKANTTADTLLQSASTVPDNAIPLAGRLSGTLVCLSGLAGALYAYLLTRRSPTPLPTTIPKTGP
>NZ_CP023445.1|WP_096491580.1|899741_900419_+|response-regulator-transcription-factor
MPTAARVLVIEDAEAIGAAVGSALREQGYQVRVRPDGRDLEGELTRFRPDLVVLDVMLPGRDGFALLEVIRRGSGAGVVMLTARDGVQDRLRGLDRGADDYVTKPFVLAEVVARVSAVLRRLGRTPSTVQIGDLVVDADSAVVVRGNAQVELTATELRLLRYLAAQRGRVVGKTQILTAVWGYEDYDPNLVEVHVSALRRKLEEHGPRLLHTVRGLGYVLRAEDS
>NZ_CP023445.1|WP_096491581.1|901811_902135_-|hypothetical-protein
MSEEPQQGRELATDAPRPPKGHHVIIAAGLVALVVLGLVIPTMRATAFAVNDDVIFYVAMYVLVFGSMYADDGMVAEMAAKQAARDEVRARRENAERAAAGEDAHES
>NZ_CP023445.1|WP_096491582.1|902229_903309_-|potassium-channel-family-protein
MKHLMGEPLSERPGHSLVGVVKMPDTVQSPVQAIMKRVIGALAALIAAVLIVYLDRDGYRDVNGDGLSLLDAVYYATVSLSTTGYGDITPASSSARLINVLVITPLRVLFLIVLVGTTLEVLTERSRQALRIQKWRTKVRDHVVVIGYGTKGRSAVSALLGDGADPGSIVVVDTAQSALDAASAIGLVTVLGSGTSNDVLKVAGVPRARAVVVAANRDDTAVLVTLTARELARDGAQVVAAVRERENEHLLRQSGADSVVVSSETAGRLLGMATATPTVVDMVEDLLTPDSGLAIAERDVEPEEVGGSPRHLSDIVLGVVRGGKLYRIDAAEADAVEAGDKLLYVKKVTPPEEDELVRR
>NZ_CP023445.1|WP_096491583.1|903308_904748_-|M20/M25/M40-family-metallo-hydrolase
MSGDPENSEHPEPPERAATTARADEFLAGLRDWLAIPSIGVDPAHHGDVARSAAWLAEALRADGWPDVRVWDEGPAQPAVYAHWPSADPDAPVVLVYGHHDVQPVDPVERWTRPPFEPTLVGEELFGRGASDDKGQVAMHLLGVRAHLAATGRTTPAVTLKLFVEGEEEGGSPHIARTLADHGPELDCDLVVFTDTPLYSREAPTVCTGQRGVYGAEVVVTGGATDVHSGRAGGSIPNPATALARLVAALHDEDGRVQLPGFYDHVVLPTDVERADYASLPFDEQVWLTNSGRARGLSGESGWSTLERVWVRPTAEVNGLVAGYTGPGLKTVVPADARVKLSFRLVPGQRPEHVAEALREFVDAHTPEGLSAEIVSRGDGVPPYAVDVAHPAVGAVRDALEGALGKPVRFSRTGGSGPAAVLHETLRVPVVYFGVALPDDNIHAPDERVVVPLLLSGAEALAVLWRTLPERLASGEPPA

Crispr_ID: NZ_CP023445_3

• CRISPR_ID: NZ_CP023445_3
• CRISPR_location: 1316575-1316671
• CRISPR_type: Orphan
• Repeat_type: I-C,I-E,II-B
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_3

Consensus_repeat	Method
GGGCCTTCCCCGCGCACGCGGGGGTGTTCCGGCGGG	CRISPRCasFinder

spacers of NZ_CP023445_3

>3.1|1316611|25|NZ_CP023445|CRISPRCasFinder
CGTGGCGGCGATCAACCAGCCCGCC

CRISPR arrays and Neighbor proteins around NZ_CP023445_3

CRISPR arrays

The CRISPR arrays of NZ_CP023445_3

>merge|NZ_CP023445|3|1316575-1316671|CRISPRCasFinder
GGGCCTTCCCCGCGCACGCGGGGGTGTTCCGGCGGGCGTGGCGGCGATCAACCAGCCCGCCGGGCCTTCCCCGCGCACGCGGGGGTGTTCCGCGGGT

>NZ_CP023445|3|2|1316575-1316671|CRISPRCasFinder
GGGCCTTCCCCGCGCACGCGGGGGTGTTCCGGCGGG	CGTGGCGGCGATCAACCAGCCCGCC
GGGCCTTCCCCGCGCACGCGGGGGTGTTCCGCGGGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_015800030.1|1311427_1311691_+|50S-ribosomal-protein-L27	unknown	unknown	gnl|CDD|235464
NZ_CP023445.1|WP_096497636.1|1325379_1326054_+|ComEA-family-DNA-binding-protein	unknown	unknown	gnl|CDD|224472
NZ_CP023445.1|WP_096491866.1|1323632_1324364_+|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl|CDD|238141
NZ_CP023445.1|WP_096491862.1|1320377_1321562_+|cytochrome-P450	unknown	unknown	gnl|CDD|225035
NZ_CP023445.1|WP_096491859.1|1315822_1316368_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP023445.1|WP_096491855.1|1304803_1306525_-|S8-family-serine-peptidase	unknown	unknown	gnl|CDD|173799
NZ_CP023445.1|WP_096491867.1|1324375_1325218_+|DegV-family-protein	unknown	unknown	gnl|CDD|273257
NZ_CP023445.1|WP_096491860.1|1316834_1318910_-|RecQ-family-ATP-dependent-DNA-helicase	unknown	unknown	gnl|CDD|223588
NZ_CP023445.1|WP_015800040.1|1322578_1323025_+|ribosome-silencing-factor	unknown	unknown	gnl|CDD|376779
NZ_CP023445.1|WP_096497634.1|1311803_1313270_+|GTPase-ObgE	unknown	unknown	gnl|CDD|237045
NZ_CP023445.1|WP_096491858.1|1314463_1315744_-|MFS-transporter	unknown	unknown	gnl|CDD|340925
NZ_CP023445.1|WP_015800029.1|1311101_1311413_+|50S-ribosomal-protein-L21	unknown	unknown	gnl|CDD|235510
NZ_CP023445.1|WP_157767526.1|1304289_1304730_-|hypothetical-protein	unknown	unknown	gnl|CDD|185594
NZ_CP023445.1|WP_096491856.1|1306768_1307524_+|DUF2344-domain-containing-protein	unknown	unknown	gnl|CDD|274865
NZ_CP023445.1|WP_096497635.1|1313290_1314403_+|glutamate-5-kinase	unknown	unknown	gnl|CDD|235460
NZ_CP023445.1|WP_096491863.1|1321564_1321786_+|ferredoxin	unknown	unknown	gnl|CDD|224064
NZ_CP023445.1|WP_096491864.1|1321860_1322454_+|nicotinate-nucleotide-adenylyltransferase	unknown	unknown	gnl|CDD|234611
NZ_CP023445.1|WP_096491865.1|1323021_1323636_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_CP023445.1|WP_096491857.1|1307715_1310631_+|Rne/Rng-family-ribonuclease	unknown	unknown	gnl|CDD|273254
NZ_CP023445.1|WP_096491861.1|1318991_1320263_+|glutamate-5-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|234685

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_015800030.1|1311427_1311691_+|50S-ribosomal-protein-L27	gnl|CDD|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	2.09452e-50
NZ_CP023445.1|WP_096497636.1|1325379_1326054_+|ComEA-family-DNA-binding-protein	gnl|CDD|224472	COG1555, ComEA, DNA uptake protein and related DNA-binding proteins [DNA replication, recombination, and repair].	2.2554e-27
NZ_CP023445.1|WP_096491866.1|1323632_1324364_+|SGNH/GDSL-hydrolase-family-protein	gnl|CDD|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	1.17068e-05
NZ_CP023445.1|WP_096491862.1|1320377_1321562_+|cytochrome-P450	gnl|CDD|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	1.19724e-100
NZ_CP023445.1|WP_096491859.1|1315822_1316368_-|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	3.09429e-33
NZ_CP023445.1|WP_096491855.1|1304803_1306525_-|S8-family-serine-peptidase	gnl|CDD|173799	cd07473, Peptidases_S8_Subtilisin_like, Peptidase S8 family domain in Subtilisin-like proteins. This family is a member of the Peptidases S8 or Subtilases serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	5.31206e-48
NZ_CP023445.1|WP_096491867.1|1324375_1325218_+|DegV-family-protein	gnl|CDD|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	1.10382e-99
NZ_CP023445.1|WP_096491860.1|1316834_1318910_-|RecQ-family-ATP-dependent-DNA-helicase	gnl|CDD|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	4.97102e-134
NZ_CP023445.1|WP_015800040.1|1322578_1323025_+|ribosome-silencing-factor	gnl|CDD|376779	pfam02410, RsfS, Ribosomal silencing factor during starvation. This family is expressed by almost all bacterial and eukaryotic genomes but not by archaea. Its function is to down-regulate protein synthesis under conditions of nutrient shortage, and it does this by binding to protein L14 of the large ribosomal subunit, thus acting as a ribosomal silencing factor (RsfS) by blocking the joining of the ribosomal subunits. This family is structurally homologous to nucleotidyltransferases.	1.16715e-46
NZ_CP023445.1|WP_096497634.1|1311803_1313270_+|GTPase-ObgE	gnl|CDD|237045	PRK12296, obgE, GTPase CgtA; Reviewed.	0
NZ_CP023445.1|WP_096491858.1|1314463_1315744_-|MFS-transporter	gnl|CDD|340925	cd17367, MFS_KgtP, Alpha-ketoglutarate permease of the Major Facilitator Superfamily of transporters. This subfamily includes Escherichia coli alpha-ketoglutarate permease (KgtP) and similar proteins. KgtP is a constitutively expressed proton symporter that functions in the uptake of alpha-ketoglutarate across the boundary membrane. Also included is a putative transporter from Pseudomonas aeruginosa named dicarboxylic acid transporter PcaT. The KgtP 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.	6.33623e-126
NZ_CP023445.1|WP_015800029.1|1311101_1311413_+|50S-ribosomal-protein-L21	gnl|CDD|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	2.0969e-42
NZ_CP023445.1|WP_157767526.1|1304289_1304730_-|hypothetical-protein	gnl|CDD|185594	PTZ00395, PTZ00395, Sec24-related protein; Provisional.	2.86687e-05
NZ_CP023445.1|WP_096491856.1|1306768_1307524_+|DUF2344-domain-containing-protein	gnl|CDD|274865	TIGR03936, radical_SAM-linked_protein, radical SAM-linked protein. This model describes an uncharacterized protein encoded adjacent to, or as a fusion protein with, an uncharacterized radical SAM protein.	1.97796e-69
NZ_CP023445.1|WP_096497635.1|1313290_1314403_+|glutamate-5-kinase	gnl|CDD|235460	PRK05429, PRK05429, gamma-glutamyl kinase; Provisional.	2.02211e-176
NZ_CP023445.1|WP_096491863.1|1321564_1321786_+|ferredoxin	gnl|CDD|224064	COG1141, Fer, Ferredoxin [Energy production and conversion].	4.47579e-09
NZ_CP023445.1|WP_096491864.1|1321860_1322454_+|nicotinate-nucleotide-adenylyltransferase	gnl|CDD|234611	PRK00071, nadD, nicotinate-nucleotide adenylyltransferase.	7.46742e-104
NZ_CP023445.1|WP_096491865.1|1323021_1323636_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.99961e-55
NZ_CP023445.1|WP_096491857.1|1307715_1310631_+|Rne/Rng-family-ribonuclease	gnl|CDD|273254	TIGR00757, Ribonuclease_E/G-like_protein, ribonuclease, Rne/Rng family. This model describes ribonuclease G (formerly CafA, cytoplasmic axial filament protein A), the N-terminal domain of ribonuclease E in which ribonuclease activity resides, and related proteins. In E. coli, both RNase E and RNase G have been shown to play a role in the maturation of the 5' end of 16S RNA. The C-terminal half of RNase E (excluded from the seed alignment for this model) lacks ribonuclease activity but participates in mRNA degradation by organizing the degradosome. [Transcription, Degradation of RNA].	1.11018e-176
NZ_CP023445.1|WP_096491861.1|1318991_1320263_+|glutamate-5-semialdehyde-dehydrogenase	gnl|CDD|234685	PRK00197, proA, gamma-glutamyl phosphate reductase; Provisional.	0

Protein sequences

>NZ_CP023445.1|WP_096491859.1|1315822_1316368_-|GNAT-family-N-acetyltransferase
MLRTERLVLRRFSAEDAGALSAYRSDPEVARYQSWEPPVPLSRALLLADEMGEADPGAPGWFQYAVVLDGELVGDIGVHLHEDLRNADIGYTFARAHQGKGYATEAVARVLEDLFTVRGVEEVGAECDSRNVASAKLVARLGFRLVERVEQAEWFKGELIDSLVFRLSAREWRRNRGGQAG
>NZ_CP023445.1|WP_096491858.1|1314463_1315744_-|MFS-transporter
MGESGGTGGGVRHRLPVRKLVAASAGNAIEWFDWTIYATFSIYFATQVFPASDERLALINTFATYALAFFFRPLGGYLLGRFADLRGRRTAMLLTIVLMAGGSLAIAALPTYEQVGWLSPALLLLARVAQGLSLGGEVSNASAYLAEIAPADRRGRYSSFFYVSTGCALLLASLLGFGLARALTTAQLASFGWRVPFLVGAVLGLAALWLRRDLEETEHFARGRAKAVELRRPLLTTLRDHPAAVGRLVGFSMASTLCYYTFFSALTPFAVKTRGADAGDVFLALSIGTLLFVALQYPMGALSDRIGRRPQMLVWTALTAVGVVPLSTLIGPGLGGLLVVFCAGLGLYTAMTSIAPAVMSELFPTELRGLGIGAWYNLTVALFGGTAPLVINVLSGAQFFWYVAAGATIAFLVVLTLPETKGAVLR
>NZ_CP023445.1|WP_096497635.1|1313290_1314403_+|glutamate-5-kinase
MSQARQAVAAAGRVVVKVGSSSLTTAEGGLDRSRLDALVDAVAARRAAGGQVVLVSSGAIAAGLAPLGITRRPRDLATQQAAASVGQLALAHAYANSFGRYDLTVGQVLLTAEDVVRRAHYRNAQRTFSRLLALGAVPVVNENDTVATAEIKFGDNDRLAALVAHLVGADALFLLSDVDSLYDGDPRLPGAQRVPEVTGPSDVDGVRAGSVGASGLGTGGMASKLAAARLAASAGIPVLLAGAADATRALSAADVGTAFTATGTRLSARRFWLGHASAATGRLVLDAGAVAAVVTRRRSLLAAGVTAVEGAFEAGDVVELVDPDGEVVARGVVAFDAAELPALIGHSSGELPPEQRREVVHADDLVPLTA
>NZ_CP023445.1|WP_096497634.1|1311803_1313270_+|GTPase-ObgE
MSRFVDRVVIHAAAGDGGHGCASVHREKFKPLGGPDGGNGGKGGDVVLVVDSQVHTLLDFHFRPHASAGSGKAGAGANRDGANGADLELRVPDGTVVMTEDGEVVADLVGEGTRLIAARGGRGGLGNASLASKARKAPGFALLGEPGESRDLVLELKSVADVGLLGFPSAGKSSLISVLSAAKPKIADYPFTTLVPNLGVITAGATVFTMADVPGLIPGASEGKGLGLDFLRHIERCAVLVHVVDCATYEDNRDPLSDIDALETELAQYTPSLSKDLAERPRVVVLNKIDVPEARDLAEIVRADVEARGLPVFEISTATREGLRELTFALARVVEEYRASRPVQESTRIVLRPTAVDDQGFTVVEDPEEEGGFIVRGERPLRWIKQTDFSNDEAVGYLGDRLARLGVEDVLIKMGAVPGAQVTIGDLVFDWEPSTPAGIAAATLTGRGTDARLEPSNRVGAGERLAAKKARRLPGSYGDWVEAAEEDV
>NZ_CP023445.1|WP_015800030.1|1311427_1311691_+|50S-ribosomal-protein-L27
MAHKKGASSSRNGRDSNPQYLGVKRFGGQVVKAGEILIRQRGTKFHPGVNVGRGKDDTLFALSAGAVEFGSKRGRKTVNIVPVEAAA
>NZ_CP023445.1|WP_015800029.1|1311101_1311413_+|50S-ribosomal-protein-L21
MYAIVKTGGKQYKVAVGDVVEVEKLDGTPGTEITFAALLVVDGSDVTADAEALGKISVTGEVVEQTKGPKIRIHKFKNKTGYHKRQGHRQKLTRVKVTGITGK
>NZ_CP023445.1|WP_096491857.1|1307715_1310631_+|Rne/Rng-family-ribonuclease
MSNTDKPAGPAGGGSATPGHPALADLPAKLRVHALAKLLGTTSKDVLAALADLGETVRSAQSSVTRDLAIKVGESLLNWDDIVTGDVDELTVTEVEAAVPAREVAALTPLFAPPSAMFLPPTPVATTAVPVTRAEPEDEDDEADDQHADASDDADGDGDGRRRRRRGRRGRGRGKGVEDNQDESAEEVDQAPAAEAEPEADEPAADASDDEEEGGGSRRRRRRRRRKSGADDESAPNEDDPPNTVVHVRETRDARDDRADSEAAQNEVRSVRGSTRLEAKRQRRRDGREAGRRRAPVLSEAEFLARREAVERTMVVRERGDRTQIGVLEDGVLVEHFVTSAGSGSLVGNVYLGRVQNVLPSMEAAFIDIGRGRNAVLYAGEVDWDAAGLEGKARKIEQALSSGDSVLVQVTKDPVGHKGARLTTQISLPGRFLVYVPGGGATGISRKLPDNERKRLKDILKRVVPDDAGVIIRTASEGVAEEELARDVTRLQAQWQIIKDKAATPKAQAPQLLYEEPDLLVKVVRDLFTEDFSGLVVQGSEAWDTIDGYVRHVAPDLQDRLHRHVGNSDAFGEYRIDEQLMKALDRKVWLPSGGYLVIDRTEAMTVIDVNTGKFTGSGGNLEETVTRNNLEAAEEIVRQLRLRDVGGIIVIDFIDMVLESNRDLVLRRLTECLGRDRTRHQVAEVTSLGLVQMTRKRVGTGLLEAFSSTCEHCRGRGLVVTTDPTAHSHGGGSHGGGSNGGSTGGNQQSSGGGRKSRRNKGGDSGEQQAEAQAAPVEQVPATEPEAPVEHPDAQDHDLEPEVQERRPGGRRAARQAAREAAKEAAKQEAAERAAAKREAEEQAPAAEVAAEPSVPAAAEPEAPAVVAEAVAPEVFAEAPAEPAAEDAEAPAKRGGRQRRRAVRREAGAAVTREAAPAPVVVVAPQPEPVAVEPSANGHVPEVKAESLVTTTTRRRVSRRAATRPAGPPKES
>NZ_CP023445.1|WP_096491856.1|1306768_1307524_+|DUF2344-domain-containing-protein
MQKLRVRYAKRGRLRFTSHRDVARTFERALRRAGVPMAYSQGFSPHPKVSWVGAAPTGVASEAEYVEVSVVDAVDPEALRAELDRAMPPGLDVLEVVQAGGGSLTERIEASAWRVELPGVDPERLSEAVSALLAAESVEVERLTKNGKRMIDVRPAVVTASVAGPASGEAPSSDAEHDAGGLSLPCGILVMVVRQLTPTVRPDDVLSALGVVADLVPPVPAKATRMAQGRLDDEGGLVDPLALDRVAVEEG
>NZ_CP023445.1|WP_096491855.1|1304803_1306525_-|S8-family-serine-peptidase
MPLLRRARAAAVSAALLATGLAAAPSASASAHPADGAGQAGPAAPGCVQTGRELRYLVVFDRGTSEPLASAEVGAACGRVEAYHPQIAVAVATSTDPGFGTRMGDDRAYSAQAEAVSRTKRKPDETAQLKSAVPETGDLTAQQWDMELVNAAAAHAVSTGSRDVVVGVLDSGVDPDHPDLVGALDPELSAGCTSGVADPARASWSPTTSPHGTHVAGTIAAADDGRGTTGVAPGVRIASVKVVDDEGFIYPEYAVCGFMWAATRGMAVTNNSYYIDPWVFTCRDQGGQSVVHEAVRRAVDYAADRGVLSVAAAGNEGADLTRPGRDALSPTNAAARPRPVDSSCLVLPAQLRNVVAVSSVGSSKVKAGYSSYGLGAVDLTGPGGDRKQPADDGVPGCVLSTVPSGYDYSCGTSMAVPHVSGVAALLASGHPEASPAELTKMLGEQAETLPCPADYDLNGTGAQDGYCTGYSEYNGFYGHGLVDAEAAVRSPLTGVGGPAGGAPGQTGSGQAGSGQAGSGSGQGGSGQAGAGQGGSGQAGSGESGPVRAGGSGERTEAGGAGTGSGTGKAATIG
>NZ_CP023445.1|WP_157767526.1|1304289_1304730_-|hypothetical-protein
MDDPQDRAARGARRNAARRRVAGVTWAAGVGATALAAALAAVLPSGATAGSATTGSATAGGPGAIGSGPAGTGSAGSGPAEYGTAEYGTAEYGTAGYSSAGHGSAGHGAAGHGAADTGATGRRGLDWGGAAPEPGRGRAHTGTGAS
>NZ_CP023445.1|WP_096491860.1|1316834_1318910_-|RecQ-family-ATP-dependent-DNA-helicase
MDDNALRALAEERLRALAGPGAVLREDQWTAIHALVALRRRALVVQRTGWGKSAVYFIATALLRSLGEGPTVIVSPLLALMRNQVDAAARAGVHAATINSANTDEWQDVQERVAAGEVDVLLVSPERLNNPDFRDTVLPSLTASAGLLVVDEAHCISDWGHDFRPDYRRLRTLLTELPAGVPVLATTATANDRVVRDVTEQLGLGAGSDALVLRGPLDRESLRLAAMRLPTAEARLAWLAERLAELPGSGIVYALTVAAADDVAAFLRERGYEVVAYSGRTDPAERQRAEEDLLANRVKALVATSALGMGFDKPDLGFVVHLGAPPSPIAYYQQIGRAGRGVERAEALLLPGPEDRDIWAYFASLAFPPERVVRQVLAALTDEPRSTAALEPVVELSRTRLEVVLKVLDVDGAVRRVRGGWVATGRPWEYDEERYGRIERARQAEQRAVLDYLDTEGCRMEFLLRQLDDPHAAPCGRCDNCTGQRVSAAVSEGAATAARERLLRPGVDVAPRKMWPTGMAAAGVSLSGRIPAGEQAATGRALGRLTDIGWGNRLRSLFAEADRELPDEVFAACVQVLSAWGWERRPVGVVSVGSRTRPELVGSFARRISEVGRLPQLGTVWLGAAVRRANSAQRLAGLVSASRVPDLSGVDGPVLLVDDQVDTGWTMTVAARLLRGAGAPEVLPFALAVTA
>NZ_CP023445.1|WP_096491861.1|1318991_1320263_+|glutamate-5-semialdehyde-dehydrogenase
MGLVTDDLREQVHEAARRARVAADELVLATRERKDAALLEMASALRARADEVLEANAKDVEAGRAGGTPENILDRLTLTEARIEGVAAGLETVAGLADPVGEVLRGSNLPNGLELRQVRVPMGVVGMIYEARPNVTVDAAGLALKSGNAALLRGSSSAEHSNTALVAVLRDALESTGLPADAVQLLPSHDRASVTHLITARGLVDLVIPRGGAGLINAVVQQATVPAIETGVGNCHVYVDAAADLDSAERIVLNSKTRRTSVCNAAESLLVHADVAAEFVPRITAALQAAGVTVHGGEGFAGEGVVPAADEDWDTEYLSMDIAARVVGSLDEAVAHIAAHGSGHTEAIVTDDVRAARLFTKRVDAAAVMVNASTAFTDGGEFGMGAEIGISTQKLHARGPMGLAELTSSKWLVWGEGHVRPSS
>NZ_CP023445.1|WP_096491862.1|1320377_1321562_+|cytochrome-P450
MEVRNYPFNEAVELRPDPTALELQEREPVSQVRLPYGGDAWLVTRHADVKTVLGDPRFSRAATLELGADLPRTFPLHRADANILTMDPPDHTRLRKLVAKGFTARRTELLRARAQEIVDDLLDAMEEQGPPADVVEALALPLPITIICEMLGVPVADRDRFRAWSDAAMSITAFTPEEVLAAAQSLREYIAGLVEDKRANPGDDVLTDLVTAHDGGGSLTATEVVTFGVTLLAAGHETTANQIANFTHTLLANPDKMAELRADPALVPRAVEELLRFTPLGGSAGFPRIATEDVELSGVTVPKGAAVFVDIPSGNRDPEVFERPHELDFHRSANPHVAFGHGVHHCVGAQLARVELQVAVGTLLARFPGLEPAGEAVFKRGRLVRGPQSLPVRW
>NZ_CP023445.1|WP_096491863.1|1321564_1321786_+|ferredoxin
MAGWSVEVDRDTCIGSGMCAAIAADHFRLDDGRATPLASPVEPSEEVVDAAESCPVEAILVRDAGGEVVAPQD
>NZ_CP023445.1|WP_096491864.1|1321860_1322454_+|nicotinate-nucleotide-adenylyltransferase
MSKRRIGVMGGTFDPVHHGHLVAASEVQARFDLDEVVFVPTGRPWQKSAREVSAAEDRYLMTVIATASNPRFSVSRVDIDRAGPTYTVDTLSDLKAAHPDDDLFFITGADALEQILSWHHADEAFSLAHFIGVTRPGYTLDDKHLPPGAVSLVEVPAMAISSTAVRDRTADGLPVWYLVPDGVVQYISKRGLYSLPG
>NZ_CP023445.1|WP_015800040.1|1322578_1323025_+|ribosome-silencing-factor
MAATDEARRLALVAANAASDKKAHDVILLDVSEQLVITDCFVIASAPNERQVGAIVDGVEEKLREAGRKPVRREGAREGRWVLLDFVDVVVHVQHSEERSFYGLERLWKDCPRIEFDAGPSSPDEDATGEDTTASSTGEAAADEVDRA
>NZ_CP023445.1|WP_096491865.1|1323021_1323636_+|histidine-phosphatase-family-protein
MTLSRLVLWRHGETDYNATGRMQGHLDSELTETGWNQARFAVPVLTAFAPELVVASDLRRARDTATVFTEATGVPLRVDARLRETRLGKWQGLTVDEIEAEWPGALGAWRFDGTISPPDGEARVEVAERAAEVVAEVDAETDGTALLCAHGGLISSLTGRLLELPVDRWGLLGGISNCHWTVFTRRPGGDPRWRLTSYNAGTTR
>NZ_CP023445.1|WP_096491866.1|1323632_1324364_+|SGNH/GDSL-hydrolase-family-protein
MRLLVIGDSLTFHGPAGPLPADDPGLWPNVAAAALGGRAELVAGFGWTARDAWWALTGDPRVWALLPRTDVLVLAVGHMDTLPSPLPTYLRQGLRYLRPDGLRRRARALYRAAQPVLSRATGGRPVALPPALTGRYLSDSLRAVRQFRPGLPAVGMVPSVHRSPLYANVHTGRAAGERAVREWAEADGVPLLDVPALVRAHLRDGLGNPDGMHWGWESHRAVGTAMAALVEAASVRRGSPGGP
>NZ_CP023445.1|WP_096491867.1|1324375_1325218_+|DegV-family-protein
MAIAIVTDSTSYLPDGFAASRGVRVVPLHVSVNGRSRLDGVDFGPRELTAALGERRRVTTSRATPQELAEVYRELLDGGADGVLSVHLSRALSGTWEAARLAAAQVDPVKVRVVDSRATAMGLGFAALAAAAAGPDLDLAERAATSAAERVRVFFCVETLEHLRRGGRIGTTAALVGTALAVKPLLHVEDGRLVPLEKVRTAGRAAARLVDLAAAAAGSGPVALAVHHLAAPERAVELAALLDERVPGASGCLISEVGAVIGAHTGPGVLGIVVLPGGFA
>NZ_CP023445.1|WP_096497636.1|1325379_1326054_+|ComEA-family-DNA-binding-protein
MGNPPGKHRSEDAPTVVFATSEGGADPPGLLLRLRGLLPSAAHHRRRVALLGVAGVGAVLAAALAAGERDAVVEQVPVLPVAEATSSSAAPPVLVVDVAGEVHAPGLVTVEDGARVADVLSRAGGVKPGASLTGLNLARKVTDGEQIAVGVPPAVGGAGPPAPVNINTATVEQLDALPGVGPVTAQRIVDHRARRGRFTSVQQLGEVEGIGGSKLAKLADLIRV

Crispr_ID: NZ_CP023445_4

• CRISPR_ID: NZ_CP023445_4
• CRISPR_location: 1354815-1354960
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP023445_4

Consensus_repeat	Method
GTCTTCCCCGCGCGGGCGGGGGTG	CRISPRCasFinder

spacers of NZ_CP023445_4

>4.1|1354839|37|NZ_CP023445|CRISPRCasFinder
TTCCGCCGGACTCATGGAGCGCGGCGGCGAGGAAGCC
>4.2|1354900|37|NZ_CP023445|CRISPRCasFinder
CTCCGAACCCGCAGGGGGTGGAGGAGACCCAGCGCGC

CRISPR arrays and Neighbor proteins around NZ_CP023445_4

CRISPR arrays

The CRISPR arrays of NZ_CP023445_4

>merge|NZ_CP023445|4|1354815-1354960|CRISPRCasFinder
GTCTTCCCCGCGCGGGCGGGGGTGTTCCGCCGGACTCATGGAGCGCGGCGGCGAGGAAGCCGTCTTCCCCGCGCGAGCGGGGGTGCTCCGAACCCGCAGGGGGTGGAGGAGACCCAGCGCGCGTCTTTCCCGCGCGGGCGGGGACT

>NZ_CP023445|4|3|1354815-1354960|CRISPRCasFinder
GTCTTCCCCGCGCGGGCGGGGGTG	TTCCGCCGGACTCATGGAGCGCGGCGGCGAGGAAGCC
GTCTTCCCCGCGCGAGCGGGGGTG	CTCCGAACCCGCAGGGGGTGGAGGAGACCCAGCGCGC
GTCTTTCCCGCGCGGGCGGGGACT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096491894.1|1361717_1363442_-|nitrite/sulfite-reductase	unknown	unknown	gnl|CDD|223233
NZ_CP023445.1|WP_015800068.1|1353465_1353714_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096491890.1|1357521_1358580_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270271
NZ_CP023445.1|WP_096497644.1|1363838_1365053_+|coproporphyrinogen-III-oxidase	unknown	unknown	gnl|CDD|180172
NZ_CP023445.1|WP_096491891.1|1358639_1359974_-|sulfate-adenylyltransferase	unknown	unknown	gnl|CDD|180120
NZ_CP023445.1|WP_096491889.1|1356702_1357491_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213260
NZ_CP023445.1|WP_096497639.1|1347217_1348258_+|2-nitropropane-dioxygenase	unknown	unknown	gnl|CDD|367316
NZ_CP023445.1|WP_096491885.1|1352430_1353399_-|zinc-binding-dehydrogenase	unknown	unknown	gnl|CDD|176227
NZ_CP023445.1|WP_096497643.1|1360870_1361557_-|phosphoadenylyl-sulfate-reductase	unknown	unknown	gnl|CDD|234997
NZ_CP023445.1|WP_096491883.1|1349920_1351393_-|amino-acid-permease	unknown	unknown	gnl|CDD|129987
NZ_CP023445.1|WP_096491882.1|1345596_1347132_+|chitinase	unknown	unknown	gnl|CDD|119350
NZ_CP023445.1|WP_096497642.1|1355744_1356599_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223673
NZ_CP023445.1|WP_096491888.1|1354566_1354770_+|hypothetical-protein	unknown	unknown	gnl|CDD|224514
NZ_CP023445.1|WP_096491893.1|1361562_1361721_-|Insertion-element-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096491884.1|1351630_1352398_+|enoyl-CoA-hydratase	unknown	unknown	gnl|CDD|236109
NZ_CP023445.1|WP_096491886.1|1353723_1354164_+|ribonuclease-N	unknown	unknown	gnl|CDD|238340
NZ_CP023445.1|WP_096491892.1|1359974_1360889_-|sulfate-adenylyltransferase-subunit-2	unknown	unknown	gnl|CDD|235375
NZ_CP023445.1|WP_096491887.1|1354160_1354499_+|barstar-family-protein	unknown	unknown	gnl|CDD|376530
NZ_CP023445.1|WP_096497640.1|1348348_1349929_+|DUF885-domain-containing-protein	unknown	unknown	gnl|CDD|377577
NZ_CP023445.1|WP_096497641.1|1355007_1355736_-|sirohydrochlorin-chelatase	unknown	unknown	gnl|CDD|225049

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096491894.1|1361717_1363442_-|nitrite/sulfite-reductase	gnl|CDD|223233	COG0155, CysI, Sulfite reductase, beta subunit (hemoprotein) [Inorganic ion transport and metabolism].	2.28578e-165
NZ_CP023445.1|WP_096497642.1|1355744_1356599_-|ABC-transporter-permease	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	2.22559e-45
NZ_CP023445.1|WP_096491890.1|1357521_1358580_-|ABC-transporter-substrate-binding-protein	gnl|CDD|270271	cd13553, PBP2_NrtA_CpmA_like, Substrate binding domain of ABC-type nitrate/bicarbonate transporters, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes nitrate (NrtA) and bicarbonate (CmpA) receptors. These domains are found in eubacterial perisplamic-binding proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding their ligand with high affinity, they 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. These binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.56619e-59
NZ_CP023445.1|WP_096497644.1|1363838_1365053_+|coproporphyrinogen-III-oxidase	gnl|CDD|180172	PRK05628, PRK05628, coproporphyrinogen III oxidase; Validated.	0
NZ_CP023445.1|WP_096491891.1|1358639_1359974_-|sulfate-adenylyltransferase	gnl|CDD|180120	PRK05506, PRK05506, bifunctional sulfate adenylyltransferase subunit 1/adenylylsulfate kinase protein; Provisional.	0
NZ_CP023445.1|WP_096491889.1|1356702_1357491_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213260	cd03293, ABC_NrtD_SsuB_transporters, ATP-binding cassette domain of the nitrate and sulfonate transporters. NrtD and SsuB are the ATP-binding subunits of the bacterial ABC-type nitrate and sulfonate transport systems, respectively. 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.	3.20347e-105
NZ_CP023445.1|WP_096497639.1|1347217_1348258_+|2-nitropropane-dioxygenase	gnl|CDD|367316	pfam03060, NMO, Nitronate monooxygenase. Nitronate monooxygenase (NMO), formerly referred to as 2-nitropropane dioxygenase (NPD) (EC:1.13.11.32), is an FMN-dependent enzyme that uses molecular oxygen to oxidize (anionic) alkyl nitronates and, in the case of the enzyme from Neurospora crassa, (neutral) nitroalkanes to the corresponding carbonyl compounds and nitrite. Previously classified as 2-nitropropane dioxygenase, but it is now recognized that this was the result of the slow ionization of nitroalkanes to their nitronate (anionic) forms. The enzymes from the fungus Neurospora crassa and the yeast Williopsis saturnus var. mrakii (formerly classified as Hansenula mrakii) contain non-covalently bound FMN as the cofactor. Active towards linear alkyl nitronates of lengths between 2 and 6 carbon atoms and, with lower activity, towards propyl-2-nitronate. The enzyme from N. crassa can also utilize neutral nitroalkanes, but with lower activity. One atom of oxygen is incorporated into the carbonyl group of the aldehyde product. The reaction appears to involve the formation of an enzyme-bound nitronate radical and an a-peroxynitroethane species, which then decomposes, either in the active site of the enzyme or after release, to acetaldehyde and nitrite.	1.2759e-74
NZ_CP023445.1|WP_096491885.1|1352430_1353399_-|zinc-binding-dehydrogenase	gnl|CDD|176227	cd08266, Zn_ADH_like1, Alcohol dehydrogenases of the MDR family. This group contains proteins related to the zinc-dependent alcohol dehydrogenases. However, while the group has structural zinc site characteristic of these enzymes, it lacks the consensus site for a catalytic zinc. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H)-binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	6.72744e-90
NZ_CP023445.1|WP_096497643.1|1360870_1361557_-|phosphoadenylyl-sulfate-reductase	gnl|CDD|234997	PRK02090, PRK02090, phosphoadenylyl-sulfate reductase.	2.82794e-101
NZ_CP023445.1|WP_096491883.1|1349920_1351393_-|amino-acid-permease	gnl|CDD|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	1.66001e-114
NZ_CP023445.1|WP_096491882.1|1345596_1347132_+|chitinase	gnl|CDD|119350	cd02871, GH18_chitinase_D-like, GH18 domain of Chitinase D (ChiD). ChiD, a chitinase found in Bacillus circulans, hydrolyzes the 1,4-beta-linkages of N-acetylglucosamine in chitin and chitodextrins. The domain architecture of ChiD includes a catalytic glycosyl hydrolase family 18 (GH18) domain, a chitin-binding domain, and a fibronectin type III domain. The chitin-binding and fibronectin type III domains are located either N-terminal or C-terminal to the catalytic domain. This family includes exochitinase Chi36 from Bacillus cereus.	4.51967e-114
NZ_CP023445.1|WP_096491888.1|1354566_1354770_+|hypothetical-protein	gnl|CDD|224514	COG1598, COG1598, Predicted nuclease of the RNAse H fold, HicB family [General function prediction only].	0.000456059
NZ_CP023445.1|WP_096491884.1|1351630_1352398_+|enoyl-CoA-hydratase	gnl|CDD|236109	PRK07827, PRK07827, enoyl-CoA hydratase family protein.	3.36864e-82
NZ_CP023445.1|WP_096491886.1|1353723_1354164_+|ribonuclease-N	gnl|CDD|238340	cd00607, RNase_Sa, RNase_Sa. Ribonucleases first isolated from Streptomyces aureofaciens. In general, ribonucleases cleave phosphodiester bonds in RNA and are essential for both non-specific RNA degradation and for numerous forms of RNA processing. RNAse Sa is a guanylate specific endoribonuclease which belongs to the superfamily of microbial ribonucleases. Typical of this sub-family, the enzyme hydrolyses the phosphodiester bonds of RNA at the 3' oxygen end of guanosine residues to yield oligonucleotides with the guanosine-2',3'-cyclophosphate at the 3' end and the hydroxyl group at the 5' end. The terminal guanosine-2,3'-cyclophosphate is hydrolysed by guanyl RNAses to give guanosine-3'-phosphate.	2.6422e-36
NZ_CP023445.1|WP_096491892.1|1359974_1360889_-|sulfate-adenylyltransferase-subunit-2	gnl|CDD|235375	PRK05253, PRK05253, sulfate adenylyltransferase subunit CysD.	0
NZ_CP023445.1|WP_096491887.1|1354160_1354499_+|barstar-family-protein	gnl|CDD|376530	pfam01337, Barstar, Barstar (barnase inhibitor).	8.62259e-25
NZ_CP023445.1|WP_096497640.1|1348348_1349929_+|DUF885-domain-containing-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	5.88284e-146
NZ_CP023445.1|WP_096497641.1|1355007_1355736_-|sirohydrochlorin-chelatase	gnl|CDD|225049	COG2138, COG2138, Sirohydrochlorin ferrochelatase [Inorganic ion transport and metabolism].	1.02344e-30

Protein sequences

>NZ_CP023445.1|WP_096491888.1|1354566_1354770_+|hypothetical-protein
MNEQPTLTAAVHREEDWHVAQCLEVDVASQGRTAAEALANLAEAVELYLEERSRSGPSGDGERGGAK
>NZ_CP023445.1|WP_096491887.1|1354160_1354499_+|barstar-family-protein
MTARAVREAQERGAHPHVLAGAEITGKRAALDAIAAALSFPDWFGRNLDALYDCLVDLSWLPEGEHVLIWPQREVFDRKDPVGSAAVDSVLRDAAEQGAEGRVLTVVYPAPL
>NZ_CP023445.1|WP_096491886.1|1353723_1354164_+|ribonuclease-N
MTPGRRLTVALVGLIALVVVGYFAKDRGNDSTPAPPSSSAGSTSVPGASASGFSVQPLSELPAQAAETWKLITSDGPFPYPRNDGVVFRNREKLLPQHKGEYYREYTVPTPGSRDRGARRLVTGQEDEVYYTADHYESFVVVDVAR
>NZ_CP023445.1|WP_015800068.1|1353465_1353714_+|hypothetical-protein
MESIARWWDGVELWLAQLPFFLQFPLVMAVLLPAALGVARFIDRVVDEASARLSGDPEAEPPVGALPTDVREPRLREGRTRS
>NZ_CP023445.1|WP_096491885.1|1352430_1353399_-|zinc-binding-dehydrogenase
MFSVYAAEPSPDQPLAALRVGERPEPEAPDGWVRVAVRAATLNMHDLWTLRGVGIKADRFPMILGCDGAGVLEDGAEVVLHSLIGSPDHVGDETLDPGRSLLTEKHQGAFADWVVVPRRNAIPKPSGLDFAEAACMGTAWLTAYRMLFVKSGLRPGQTMLVQGASGGVSTALVQLGRAAGYRVWVTGRTEAKRALAESLGAHATFESGARLPERVDAVFETVGRATWSHSMKSLKPGGVVVVSGATTGDPSAVELQRLFFLQLRVVGSTMGTRDELVDLLAFCERNGLRPHIGSRLPMADAEAGFRAMLDGETAGKTVFTLG
>NZ_CP023445.1|WP_096491884.1|1351630_1352398_+|enoyl-CoA-hydratase
MAAEQLVRYEVRRGVATVVLDSPRNRNALSARLRRELLAHLVTALADDAVRVVVLTHTGPVFCSGMDLKEAQGAASADQGVNEFPEILKTLWASPKPVVARLAGPARAGGVGLVAACDVAVAVDSATFAFSEVRIGVVPAIISVTVLPRLSSRAAHELFLTGEVFDAGRAARIGLVNSVVAEGGLDAEVARFTDMLVLGAPGALAATKAMLQRGTDVDAAFADMLRLSAAHFGGPEGQEGIAARLEKRKPDWVPE
>NZ_CP023445.1|WP_096491883.1|1349920_1351393_-|amino-acid-permease
MSAHSGFGQGRGVFRRKPVLEGDSPHQGGGLTRTLGLWQLTAIGVGGIIGAGIFSLAGAVANKTAGPAVLISFLVAGIASAAAAFSYAEFAGLIPQAGSAYTYGYAVLGEIVGWFIGWDLLLEYTAIVAVVAIGISGYFNELLSLLGLHLPEWMLGAPGTESGDAAPGSYKVNLFAALLCLLIAFVLNQGMKNAARFETTLVYLKVAVVLLVVVVGAFHIDTANYNPFFPFGISGALTGAATVFFAVFGYDAMSTAAEESTDSRKHMPKAILYSLAISMVLYALACLVLTGMVPYSQVDTESAFATAFADVGLPALGIVISVGAVLGITTVLFTFLMGAARVGYSMSRDGLLPRWFAKTHPTKHVPTRTTWVLGAASAVIAGFLPIAEAAELTNIGILLAFVVVCVAVIVLRYRRPDLPRTFRTPGMPVVPVVGVVFSLWLITFLAPETWLRFAVWFAIGLVVYYAYGKRHSVLADQGGRSADRNEPGSG
>NZ_CP023445.1|WP_096497640.1|1348348_1349929_+|DUF885-domain-containing-protein
MATLIGVPGWDDRLPDPSAEAEAGAARRAAELATRAAEGDDDPITRAVVAQQAAGTVAKLGARLVEHTHAEGFNAPVPLLLTSLSMVRPASGQGELDYLARLRAVPGYLEALATRQLDSDRRPLAHLVDAAVTRLDRHLADPSGPLRVPPLSAGPAAERERLITELVDPALARYRDVLRERVAPRGRSADEPGLCWLADGERHYAGLVAAYTTTERTARELHEVGLGLVAELDREYEEIGARVFGPLPGADARERAAGVRARLLADPELRWTDGAQMVELARRVLARAELAAGDWFGSVPAKRCAVATVPDDEAPNAPLAYYVDPAVDGSRPGTYFVNTHRAAERNRVSAEAVAFHEGVPGHHFQISLAQELTDLPPLRRFAAFEAYLEGWGLYAERLADEMGLYSGDLARLGMLSADSLRAARLVVDTGMHALGWTRERAVEYLRASTAAPEADVQAEVDRYIEAPAQALSYMVGRLEIQRLRGVASDRLGAAFDIRAFHDLVLRGGPLPLGVLADVVDRWCGSA
>NZ_CP023445.1|WP_096497639.1|1347217_1348258_+|2-nitropropane-dioxygenase
MLESLPVPVIAAPMAGGPSTPELVAAVGGAGGLGFLPAGYLTPDALADRIARTTALSPAPFGVNLFVPGPDGGVEEARAYRRLLVEESGLEPGEPRWDDDSYPAKLELLLALRVPVVSFTFGLPSASDVDRLRAAGTTTVATVTTPAEAEQAARVGVDALCVQGIDAGGHRGTFADDGRSPGGGELIGLLTALRLVGARVSLPLIAAGGIAHGADVAAVLAAGAVAAQLGTAFLACPEAGTAPAHRKALAEGTRRTALTRAFSGRPARGLVNRFLTEHTPHAPAAYPRVHHLTKPIRASGDPELMSMWAGQAYPLARSVPAAQLVADLNAQAVEALARANARIRPL
>NZ_CP023445.1|WP_096491882.1|1345596_1347132_+|chitinase
MAGKTARALGALTAAALTITGAILLAQGSASAANLVSNAGFDTGSTSGWTCSGKSSAVTSPKRSGSHALSATPEGSDNARCSQTVQVRPNTAYSLSAWVQGSYVYLGVSGTGGDDKNTWTPGSTGFSELKLGFTTGPSATTATVYLHGWYGQPTYYADDVVLDGPGGTQPTTTTPPVTTTKPTTTTKPTTTTTKPTTTTPPTTTTSNNPGQPDPALPKHLLTGYWHNFDNGSKALRLADVPRAYDVVAVSFADAVPTRPGAVSFTLDPGLAGKLGGYTDAQFKADVKTLQSRGQKVIISVGGERGTISVGDSTASANFASSVKDLVASYGFDGVDVDLENGVNATHMAPALRAIHAAGGKIITMAPQTIDMQSTGTEYFKLALAVKDILTVVNMQFYNSGAMLGCDQKVYSQGTVDFLVSLACVQLENGLRPDQVGLGLPSSGSAAGGGYQSPANVNAALDCLARGTSCGSFKPAKTWPGIRGAMTWSINWDATANWQFSNTVAPHLKTLP
>NZ_CP023445.1|WP_096497641.1|1355007_1355736_-|sirohydrochlorin-chelatase
MAVAHGSRDPRSAAVVNELLGVVRALRPELDVRASFLELSAPRLPDVLRAVRADGHREAVVVPLLLGRAYHARVDVPSAVAEAAVLGLDVAIADVLGPDPRLESAALRRLAEAGVGFGDPSWGVVLAAAGSSHARANAVVRATARRWAAGAGWAGVEPAFAASAAPDAAVAAARLRAAGARRVAVASWFLAPGLLPDRVTGLVGADAVVAAPLGADPEVAELVLHRYAGARVRAAGRVTAIA
>NZ_CP023445.1|WP_096497642.1|1355744_1356599_-|ABC-transporter-permease
MAAVGAGLDALDTPIGERPPSVWRRVARTALPPLVAFALLLVVWQALWAAALWPEYRLPSPLSVWGAVAEAVRTGRAAEVLWTSVHRAVLGFLAAVVIATPLGLLIAKVRLVRAAIGSLLSGLQSLPSVAWVPAGILWFGATPATIYFVVLMGSVPSIANGLVAGIDQVPPLLPRVGQALGAGRLASARHILLPAALPGYLAGLKQGWAFSWRSLMAAEIIATSPQLGEGLGQYLHNGASLNDISMVIAAIFLILLVGVGIELLLFRPLERAVLRARGLTGALA
>NZ_CP023445.1|WP_096491889.1|1356702_1357491_-|ABC-transporter-ATP-binding-protein
MTATLGTTAPRSGVDAAVTLTGVRKEFGTGQHAVVALDGVDLQVAPGEFVCLLGASGCGKSTLLNLVAGLDAPTSGRIGLTTSRPAVMFQEAALMPWLTAERNVELPLRLAGVRRGERRARAGELLELVRLSGVGRKRPHELSGGMRQRVALARALASTQGSADGGAPGLLLMDEPFAALDAITRDVLQSELARVWRETGTAVLFVTHDVREAVRLGQRVVLLSSRPGRIVREWAVEGRDPAELIEDVTGRLREVISGHAAA
>NZ_CP023445.1|WP_096491890.1|1357521_1358580_-|ABC-transporter-substrate-binding-protein
MKTTAVLLAALAVATGCSRAERAEESAPAADQGAAAELRLGYFPNVTHASALIGVERGLFERELGSTKLTTQTFNAGPEAVNALLGESLDATFIGSGPAINAYAKSGGEAVKLIAGATSGGAQLVVKPEITSPQDLKGKVITTPQLANTQDVALKKWLSDQGLAIGAGPDQVNVTNTENSQSLDLFRSGGVQGAWAPEPWSSRLVVDAGAKVLLDEKTLWEGGKFPTTVLIVRTEFLQEHPQTVQALLRGHLAATKYARDDAAGAKTTVNEALKKLTGKALGEPVLNRAFEGIELTLDPQASAFPQLAEDAVTAGVAKEAADVAGLADFGPLNEVLKAAGEPAVDAAGLDRK
>NZ_CP023445.1|WP_096491891.1|1358639_1359974_-|sulfate-adenylyltransferase
MSDLLRLATAGSVDDGKSTLVGRLLYDTKSVLADTLDAVQRASADRGLATPDLSLLVDGLRSEREQGITIDVAYRYFATPRRTFVLADTPGHVQYTRNTVTGASTAQLAVLLVDARRGVVEQTRRHAAVLALLGVPRLVLAVNKVDLVGYDEVVFSRIAKEFAAHASALGFAEDSVVSIPVSALVGDNVVDRSASTPWYSGPTLLEHLESVPVEPDPHDAPFRFPVQYVIRPRTAEHPDYRGYAGQVAAGTVRVGDEVTVLPGGSRTTVTGIDTADGPLAEAAAGRSVTLLLAHDLDVSRGDLIAAGDAPEVVDEFTATLCWLAEKPLAPGARVLVKHGTRTVQAIVTELLSRFDEQALASTGAPDALRLNDIGQVRVRTAEPVPVDDYTRDRRTGAFLVIDAGDGGTLAAGLVGAPLPEPDAPGAQAGGVALADGRALVSPGP
>NZ_CP023445.1|WP_096491892.1|1359974_1360889_-|sulfate-adenylyltransferase-subunit-2
MRVARMTLALDALDRLESEAVHIFREVAGEFDRPVILFSGGKDSTLLLHLAVKAFWPAPVPFPLLHVDTGHNFDEVIAFRDEVVARHGLRLEVARVQDYLDDGRLAERPDGTRNPLQTVPLLDAITANRFDAVFGGGRRDEERARAKERIFSLRNAFGQWEPRRQRPELWNLYNGRHRAGEHVRVFPLSNWTELDVWHYIARERIELPPIYYAHRREVYLRDGMWLAQGPWGGPRAGEELVEKTVRYRTVGDGSCTGAVESEAADIDAVIAEVAASRLTERGATRADDRMSEAAMEDRKREGYF
>NZ_CP023445.1|WP_096497643.1|1360870_1361557_-|phosphoadenylyl-sulfate-reductase
MEEDLRVVAEAAQAELADATAEEALAWTARTFGDSWIVASNMQDAVLVDLAAKVKPDVDVLFLETGYHFAETIGTRDAVDLVYPELRIVNAAAEQSAADQEAEFGPLNRTDPSRCCHLRKVVPLRRTLAGYDAWVTGVRRVDAPTRADTPIVQWDERNGLVKVNPIAPWSDDEFNGYLAEHKILENPLVQAGYPSIGCAPCTAKPLPGADPRSGRWAGTAKTECGLHG
>NZ_CP023445.1|WP_096491893.1|1361562_1361721_-|Insertion-element-protein
MSERATPFHCPYCGDEDLRPQEEPAHAWLCSACRRVFTVKFIGLNLPQEVRG
>NZ_CP023445.1|WP_096491894.1|1361717_1363442_-|nitrite/sulfite-reductase
MVPPTTSPPTTTPTTPPSTPASPRARQRRGEGQWALGYREPLNPNERSKKDDNPLNVRARIESIYAPGGFASIDPADLRGRFRWYGLYTQRKPGIDGGRTATLAPEELDDEHFMLRVRVDGGRLTTAQLALIGELSQTYARDTADITDRQNVQYHWIRIEDVPTLWERLEAAGLTTMEACGDSPRVVLGSPLAGIAEDEVLDGGPAIDEILRRYIGDPRFSNLPRKFKTAISGLPDVAHEVHDVAFVGVVHPEHGPGFDLWVGGGLSTNPMIAKRLGAWVPLDEVPDVWEGVISVFRDYGYRRLRNRARLKFLVADWGAEKFRQVLEDEYLHRKLLDGPAPEVPEIARDHVGVHRQKDGLFAVGAAPIAGRVSGSTLVEVAKAVERAGSNRVRLTPQQKLVVLDVPEAEVDGLRADLAALGLPTEPSPWRRGVMACTGLEFCKLAIVETKARAAELVTALEARLADVVAGVAAPISVHLNGCPNSCARIQTADIGLKGQIVTDADGRQVEGFQVHLGGGLGLDAGFGRKLRGHKVTAAELPEYVERVVRHYLAGRDGDERFAQWVARADEGLLR
>NZ_CP023445.1|WP_096497644.1|1363838_1365053_+|coproporphyrinogen-III-oxidase
MPSALPAGDPAPSDGALPATALEGLGTRPFGVYVHVPFCATRCGYCDFNTYTAGELGTSASPESWLEGLRRELDLAARVLGEPPAAETVFVGGGTPSLLGADGLAAVLEAVRSSVGLAPGAEVTTESNPESTSPGFFAAIREAGYTRVSLGMQSAARHVLRILDRKHTPGRAAAAAREAREGGFEHVNLDLIYGTPGERDEDLRESLAVVRDAGVDHLSAYALIVEEGTALARRVRRGELPAPDDDVLAERYEMVDAAAREMGMSWYEVSNWAASEEGRCRHNVLYWQGADWWGAGPGAHSHVGGVRWWNVKHPAKYAAVLAGGGSPAAGREVLAEDDRRVERVLLELRLSEGLPVEVLDRDGRREAARVAAEGLLEPMALARGRCVLTDRGRLLADAVVRRLT

Crispr_ID: NZ_CP023445_5

• CRISPR_ID: NZ_CP023445_5
• CRISPR_location: 2537358-2537428
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP023445_5

Consensus_repeat	Method
CAGCCCGCGAAGTGGTCAGCCCG	CRISPRCasFinder

spacers of NZ_CP023445_5

>5.1|2537381|25|NZ_CP023445|CRISPRCasFinder
TGAAGCCGCCAGCCCGTGAAGCCGC

CRISPR arrays and Neighbor proteins around NZ_CP023445_5

CRISPR arrays

The CRISPR arrays of NZ_CP023445_5

>merge|NZ_CP023445|5|2537358-2537428|CRISPRCasFinder
CAGCCCGCGAAGTGGTCAGCCCGTGAAGCCGCCAGCCCGTGAAGCCGCCAGTCCGCGAAGTGGTCAGCCCG

>NZ_CP023445|5|4|2537358-2537428|CRISPRCasFinder
CAGCCCGCGAAGTGGTCAGCCCG	TGAAGCCGCCAGCCCGTGAAGCCGC
CAGTCCGCGAAGTGGTCAGCCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096492776.1|2541101_2542301_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP023445.1|WP_096492767.1|2527574_2528540_+|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP023445.1|WP_096492769.1|2528824_2529172_+|Sec-independent-protein-translocase-subunit-TatA	unknown	unknown	gnl|CDD|234797
NZ_CP023445.1|WP_096492771.1|2530677_2531580_+|sphingosine-kinase	unknown	unknown	gnl|CDD|237021
NZ_CP023445.1|WP_157767592.1|2544056_2547404_+|hypothetical-protein	unknown	unknown	gnl|CDD|276809
NZ_CP023445.1|WP_096497734.1|2537455_2538400_-|5'-3'-exonuclease	unknown	unknown	gnl|CDD|214682
NZ_CP023445.1|WP_096492779.1|2548372_2549911_-|aspartate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|223154
NZ_CP023445.1|WP_096492763.1|2523802_2525161_+|Pup--protein-ligase	unknown	unknown	gnl|CDD|274725
NZ_CP023445.1|WP_096492778.1|2547414_2548362_-|peptidase-S58-DmpA	unknown	unknown	gnl|CDD|239070
NZ_CP023445.1|WP_096492768.1|2528565_2528847_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_041837624.1|2539642_2540083_+|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|214628
NZ_CP023445.1|WP_096492770.1|2529314_2530427_+|twin-arginine-translocase-subunit-TatC	unknown	unknown	gnl|CDD|376413
NZ_CP023445.1|WP_096492780.1|2550085_2551771_-|DEAD/DEAH-box-helicase	unknown	unknown	gnl|CDD|223587
NZ_CP023445.1|WP_096492772.1|2531757_2534694_+|DEAD/DEAH-box-helicase	unknown	unknown	gnl|CDD|226947
NZ_CP023445.1|WP_096492774.1|2538506_2539637_+|aminopeptidase-P-family-protein	unknown	unknown	gnl|CDD|223085
NZ_CP023445.1|WP_096492775.1|2540126_2540873_-|class-IV-aminotransferase	unknown	unknown	gnl|CDD|236438
NZ_CP023445.1|WP_096492773.1|2534832_2535519_+|DUF4333-domain-containing-protein	unknown	unknown	gnl|CDD|379513
NZ_CP023445.1|WP_096492764.1|2525306_2526191_+|ATPase	unknown	unknown	gnl|CDD|176908
NZ_CP023445.1|WP_096497735.1|2542665_2543892_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_CP023445.1|WP_096492766.1|2526594_2527578_+|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP023445.1|WP_096492767.1|2527574_2528540_+|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	9.9e-55	180.9	0.1
NZ_CP023445.1|WP_096492766.1|2526594_2527578_+|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	6.2e-47	155.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096492776.1|2541101_2542301_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.16855e-34
NZ_CP023445.1|WP_096492767.1|2527574_2528540_+|YafY-family-transcriptional-regulator	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	5.36922e-45
NZ_CP023445.1|WP_096492769.1|2528824_2529172_+|Sec-independent-protein-translocase-subunit-TatA	gnl|CDD|234797	PRK00575, tatA, Sec-independent protein translocase subunit TatA.	6.39927e-20
NZ_CP023445.1|WP_096492771.1|2530677_2531580_+|sphingosine-kinase	gnl|CDD|237021	PRK11914, PRK11914, diacylglycerol kinase; Reviewed.	2.87869e-72
NZ_CP023445.1|WP_096497734.1|2537455_2538400_-|5'-3'-exonuclease	gnl|CDD|214682	smart00475, 53EXOc, 5'-3' exonuclease.	7.78474e-77
NZ_CP023445.1|WP_096492779.1|2548372_2549911_-|aspartate-aminotransferase-family-protein	gnl|CDD|223154	COG0076, GadB, Glutamate decarboxylase and related PLP-dependent proteins [Amino acid transport and metabolism].	6.62893e-75
NZ_CP023445.1|WP_096492763.1|2523802_2525161_+|Pup--protein-ligase	gnl|CDD|274725	TIGR03686, pupylate_PafA, Pup--protein ligase. Members of this family are the Pup--protein ligase PafA (proteasome accessory factor A), a protein shown to regulate steady-state levels of certain proteasome targets in Mycobacterium tuberculosis. Iyer, et al (2008) first suggested that PafA is the ligase for Pup, a ubiquitin analog attached to an epsilon-amino group of a Lys side-chain to direct the target to the proteasome. [Protein fate, Degradation of proteins, peptides, and glycopeptides].	0
NZ_CP023445.1|WP_096492778.1|2547414_2548362_-|peptidase-S58-DmpA	gnl|CDD|239070	cd02252, nylC_like, nylC-like family; composed of proteins with similarity to Flavobacterium endo-type 6-aminohexanoate-oligomer hydrolase (EIII), the product of the nylon oligomer degradation gene, nylC. EIII is an amide hydrolase that catalyzes the degradation of highly-polymerized 6-aminohexanoate oligomers. Together with other nylon degradation enzymes, such as 6-aminohexanoate cyclic dimer hydrolase (EI) and 6-aminohexanoate dimer hydrolase (EII), EIII plays a role in the detoxification and biological removal of the synthetic by-products of nylon manufacture. EIII shows sequence similarity to L-aminopeptidase D-amidase/D-esterase (DmpA), an aminopeptidase that releases N-terminal D and L amino acids from peptide substrates. Like DmpA, EIII undergoes autocatalytic cleavage in front of a nucleophile to form a heterodimer. DmpA shows similarity in catalytic mechanism to N-terminal nucleophile (Ntn) hydrolases, which are enzymes that catalyze the cleavage of amide bonds through the nucleophilic attack of the side chain of an N-terminal serine, threonine, or cysteine.	2.69558e-47
NZ_CP023445.1|WP_157767592.1|2544056_2547404_+|hypothetical-protein	gnl|CDD|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	0.00091277
NZ_CP023445.1|WP_041837624.1|2539642_2540083_+|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|214628	smart00344, HTH_ASNC, helix_turn_helix ASNC type. AsnC: an autogenously regulated activator of asparagine synthetase A transcription in Escherichia coli).	3.05249e-36
NZ_CP023445.1|WP_096492770.1|2529314_2530427_+|twin-arginine-translocase-subunit-TatC	gnl|CDD|376413	pfam00902, TatC, Sec-independent protein translocase protein (TatC). The bacterial Tat system has a remarkable ability to transport folded proteins even enzyme complexes across the cytoplasmic membrane. It is structurally and mechanistically similar to the Delta pH-driven thylakoidal protein import pathway. A functional Tat system or Delta pH-dependent pathway requires three integral membrane proteins: TatA/Tha4, TatB/Hcf106 and TatC/cpTatC. The TatC protein is essential for the function of both pathways. It might be involved in twin-arginine signal peptide recognition, protein translocation and proton translocation. Sequence analysis predicts that TatC contains six transmembrane helices (TMHs), and experimental data confirmed that N- and C-termini of TatC or cpTatC are exposed to the cytoplasmic or stromal face of the membrane. The cytoplasmic N-terminus and the first cytoplasmic loop region of the Escherichia coli TatC protein are essential for protein export. At least two TatC molecules co-exist within each Tat translocon.	2.57025e-78
NZ_CP023445.1|WP_096492780.1|2550085_2551771_-|DEAD/DEAH-box-helicase	gnl|CDD|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	8.73179e-154
NZ_CP023445.1|WP_096492772.1|2531757_2534694_+|DEAD/DEAH-box-helicase	gnl|CDD|226947	COG4581, COG4581, Superfamily II RNA helicase [DNA replication, recombination, and repair].	0
NZ_CP023445.1|WP_096492774.1|2538506_2539637_+|aminopeptidase-P-family-protein	gnl|CDD|223085	COG0006, PepP, Xaa-Pro aminopeptidase [Amino acid transport and metabolism].	1.16594e-102
NZ_CP023445.1|WP_096492775.1|2540126_2540873_-|class-IV-aminotransferase	gnl|CDD|236438	PRK09266, PRK09266, hypothetical protein; Provisional.	3.8712e-80
NZ_CP023445.1|WP_096492773.1|2534832_2535519_+|DUF4333-domain-containing-protein	gnl|CDD|379513	pfam14230, DUF4333, Domain of unknown function (DUF4333). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 140 and 255 amino acids in length. There are two completely conserved C residues that may be functionally important.	6.87465e-19
NZ_CP023445.1|WP_096492764.1|2525306_2526191_+|ATPase	gnl|CDD|176908	cd08899, SRPBCC_CalC_Aha1-like_6, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	3.31085e-13
NZ_CP023445.1|WP_096497735.1|2542665_2543892_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	4.84571e-56
NZ_CP023445.1|WP_096492766.1|2526594_2527578_+|WYL-domain-containing-protein	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	2.1559e-41

Protein sequences

>NZ_CP023445.1|WP_096492773.1|2534832_2535519_+|DUF4333-domain-containing-protein
MTSPYGPSGGNDPQQQWGQQPYGGGGYPGTPSGGFPAQQPGYGQPDPSQQHQQHQQQWGQQAPQGQPYPPQQQYPGTPGGGFDPNNPYGQQPQQPGYGQPGQYGQPGQFGGQPGQYGPPPPAKKSNGLIWGVVAAVVLIVAVVGIGGFVTPGWFNKKVLDNTSVQNGIVQVLKDDYKLDAKSASCSGEHEVKPNTTFECDVKVGDADKKVKITIKTSDGEYEVGQPTG
>NZ_CP023445.1|WP_096492772.1|2531757_2534694_+|DEAD/DEAH-box-helicase
MSSASRSPAEAYAESRRRASRPQLTDFLSVVSFELDPFQLRACEFLEDGHGVLVCAPTGAGKTVVGEFAVHLALAEGRKCFYTTPIKALSNQKYADLCARYGQDKVGLLTGDTSVNGDAPVVVMTTEVLRNMLYAGSSTLNSLGYVVMDEVHYLADRFRGPVWEEVILHLPESVRLVGLSATVSNAEEFGEWLVTVRGDTAVVVDEHRPVPLWQHMLAGPRMFDLFADDVADTHVKINPQLLRQVEDLARFHVPWTRGRGNKGGRPPRSTGFKPPSRVDVIQRLDAAGLLPAIVFVFSRAGCDAAVNQCVRYGLRLTTPDEVEVIRRIVDEKTRDLPQDDLMVLGYWEWREALERGIASHHAGLLPAFKETVEELFVRGLVKAVFATETLALGINMPARTVVLEKLVKYNGEAHVDLTPGEYTQLTGRAGRRGIDVEGHAVVVWQPGVDPKAVGGLASTRTYPLRSSFRPGYNMAVNLVHRLGAPAARDLLEQSFAQFQADRSVVGLARRIERNREALAGYAESMSCHLGDFTEYASLRRRVTDREKALARQNTSASRAETAASLERLRKGDVIAVPSGRRTGLAVVIDPGLEPLGEPRPFVVTEDRWAGRLTSADFPLPVEVLGKVRLPKQVDTRSPRSRRDLAATLRNTGLVAPSARKRRSTADDDAELATLRRALRAHPCHGCEKREEHARWGERYHRLLAETEQTERKVAATTHSLAREFDRIRGLLRERGYLEVVEDEPESEGGAVFEAPGEGAVSEGGASEGAASGGGAEGEPGQRKRRVVRRAGQERVSGGPGRRGGERVTEHGRRLTRLYSESDLLAAECLRHGVWKGLAPEELAAVVSSLVYEARRDGPMETRLPPGKVSDAMTATARLWAELEDDERRHRLDRTRQPDPGFAWAVYRWARGESLERVLGTTDTGGTELGAGDFVRWCRQVVDFLDQIRDVVGGGDPVGAAARKAVDALRRGVVALATV
>NZ_CP023445.1|WP_096492771.1|2530677_2531580_+|sphingosine-kinase
MTRAALLVSPNSGGGAAARIAGTTAALLREAVDVLDLLVPTSTAEAAAMAERVVGANVDALVVLGGDGAAHVALQACAGTPTALAVIPAGTGNDLARALGSRSAADLVPALRSGERRRVDLGRVRGGRWFATVLCAGFDSAVNARANRMRWPAGPRRYDLALLAELLGPRPGRLLLGTPKGEIGVNALLVAVGNTGSYGGGVPVCPWADPEDGLFDVTVVEAVSRRTLLRVLPTLRTGDHTAHPAVHTFRASSIRLAGPAWTAYADGERQRALPVTATCVPGALSTIPSALTDSSIPARA
>NZ_CP023445.1|WP_096492770.1|2529314_2530427_+|twin-arginine-translocase-subunit-TatC
MSRRRESRKLRSRRHNPEGTMSLRDHLYELRNRLGWALLFLTIGAIFGFIWWSWRILGAPSLGDIIISPYCGIPLEDRFNQNQECQLLQTQPFEAFMIQLKVGAAAGAVLTSPLWLNQLWRFIAPGLYAKERKFALIFVGVASLLFLAGAVLAFYVVPQGLSVLVGFGDNKFLTALSGTAYIDFVLALLIIFGVSFELPLVVVMLNAVGILPYEKLKRWRRGLIFGLFVFAAFATPGTDPISMVALAISLALLFEMATQIARLHDKRKARKRVEEGFGPEENWDGLSDDEASPFDYTPSQVEDGGQARTATQTAQHQTAQHQTAQHQTAQHQTAQHQPQTAPPQPQAPAQPTPPPTAQPERRVNYDDDAT
>NZ_CP023445.1|WP_096492769.1|2528824_2529172_+|Sec-independent-protein-translocase-subunit-TatA
MPNLGVPELLIIAVVVLLLFGSKKLPDMARSLGRSAKILKAETKGLRDEDQPQQQPVQQVQPVQQPVQPLPTAQQPVQQYAQPVQQPVAQPVQQQPVAQPVAQQPVAQPVQPKQD
>NZ_CP023445.1|WP_096492768.1|2528565_2528847_+|hypothetical-protein
MPYLPSLALVLLGLVILVVAVLKVTRSLRRARAASTLMSDRVGDRVGFLRARLAALGVAFRQRRPDKARQGEPRLRSRNRGRQEEHHAQSRSA
>NZ_CP023445.1|WP_096492767.1|2527574_2528540_+|YafY-family-transcriptional-regulator
MTSANDRLPRLLALVPYLLARPGIPIDEAAADFQVTPKQLRKDLELLWMCGLPGYGPGDLIDLSFEGETVTVTFDAGMSRPLRLTAAEATSLLVALRALADTPGVADKAAVERAVAKVESAVGQAQPSGVAVGLAVREGPETARVRDAIAEGVRARRALALRYYTPSRDEITDRVVDPMRMLLVEGRSYLEAWCRAADGVRLFRIDRVDAVEVLDEPASPPPHAVPTDTSEGLFQPDPDQRAAVLVLEPDARWFAEYYPTEALVELPDGRARVLMRYTDTAWMVRLVLGQGGEVRAEEPAELVEAVARQARAALDRADQLR
>NZ_CP023445.1|WP_096492766.1|2526594_2527578_+|WYL-domain-containing-protein
MATARAERLVNLVLCLLSTRQYLTAERIRAIVPGYTDAATDEAFFRMFERDKSELRDLGVPLETGRSGAFDSVDGYRIARRDYELGDIDLEPDEAAAVALAGRLWDSPQLTGAAHGALLKLRAAGVDVDQDVHVPVEPRVRATEPAFPPLLAASQTGRVVEFDYRRPSPVEVRTRTVEPWGVVAWRGRWYLVGHDRDRGATRCFRLSRIVGDVRTLGKPGAVTRPDDVDLLGFVARTQPSPQPPAPAKLWVAKGRGHGLRRRARVVGERELAGVPGDLLEIELNFPDSAAGWIAGFGPDAVVLEPEVLAKSVRERLLGALRGTGVVV
>NZ_CP023445.1|WP_096492764.1|2525306_2526191_+|ATPase
MSETVRLAVRAGVPVERVWRALTEQAEVRAWLAEEAEVDLPTRFTFGGRQSPGGEQRVLAVVDGAAGDRGLTLGWDVGGEQTTVEFRLVAEGGSTQVHLAQSHFPGWEAAVAEEGVLAWLYTFWVLALCDLVDHVEGREVGPRPDFTPGLAEFRAEVLIRAPRPEVAASLVEPERYERWFGAKVDIEPWPGGRFAMGGSDLDPSPGQVAAYEPDRMMRIAWGRSTHTWELSDAEEGTTLVVTQSGFDPDHPPHGEWSGWLGGLAGLRRYHELPNTPPIWLPGDVPGLPEGMLTD
>NZ_CP023445.1|WP_096492763.1|2523802_2525161_+|Pup--protein-ligase
MQRRIFGIETEFGVTCTFHGQRRLSPDEVARYLFRRVVSWGRSSNVFLRNGSRLYLDVGSHPEYATAECDDLAQLVSHDKAGERILEDLLVDAERRLADEGIGGDIFLFKNNTDSAGNSYGCHENYLVARAGEFSRIADVLLPFLVTRQLICGAGKVLQTPRGAVYCLSQRAEHIWEGVSSATTRSRPIINTRDEPHADAERYRRLHVIVGDSNMSEVTTLLKVGSANLVLEMIEQGVQFRDFSLDNPIRAIREISHDLTGRRTVKLAGGKEASALDIQREYYERAVEHVAKRSPDPMAERVLELWGRTLDAVAAQDLSKIDREIDWAIKHRLLERYQAKHDMDLSNPRIAQLDLAYHDIRRGRGVFDLLQRKGQVERVTDDGEIEAAKDTPPQTTRAKLRGDFIAAAQAAGRDFTVDWVHLKLNDQAQRTVLCKDPFRAVDERVERLIASL
>NZ_CP023445.1|WP_096497734.1|2537455_2538400_-|5'-3'-exonuclease
MSSPLVLMDAASLYFRSFYALPESMTAPDGTPVNAVRGFVDTIAKIVNDRNAARLVACLDADWRPEFRVAALPSYKAHRVAESGDAEEVPDTLTPQVPIILDVLDAVGIATAEAPGHEADDVIGTLVARETTAPVEVVTGDRDLFQVVRTTPTPAGVLYLGRGWAKAELVGPAELAAKYALPEQNAGRAYADMAVLRGDPSDGLPGVAGIGEKTAAKLITEFGSLEAVLAAVHDGRDRKLTTKARNALIAAEDYLAAAPTVVNVALDAPVTQDRDDTLPATPADPDRLTELTKRWGLGSSVPRLLTALERRAER
>NZ_CP023445.1|WP_096492774.1|2538506_2539637_+|aminopeptidase-P-family-protein
MSTRVGPLDVEALRSRLDRATAAAAVAGVDALLISPGSDLRYLIGAGGASFERLTCLVVPVGGDPVLVVPKLEQPGYAAVPTEALGVEVATWVDGEDPYALVRKALKGTARTAVADMTPALHVLGLRGAIGGEQVLAGPILRELRMRKDAAEIAALRKAGEAIDRVHARVGEWLRAGRTEAEVGADIAAAIVAEGHEVAEFVIVGSGPNGASPHHSLSDRVIEVGDVVVVDIGGPVAEGYNSDSTRTYSIGEPRDADVRETYAVLQAAQQAAVDAARPGVTCEAVDAAAREVIDAAGFGQYFVHRTGHGIGLDVHEEPYIVAGNDLPLEAGMAFSVEPGIYLPGRWGARIEDIVIATGSGSERLNNRPHELVVLEA
>NZ_CP023445.1|WP_041837624.1|2539642_2540083_+|Lrp/AsnC-family-transcriptional-regulator
MEPIDRAILRELSTDGRCSFTDLAERVGLSVSAVHQRVRRLEQRGVVKGYAARLDGDEVGLPLTAFISLTPIDPAAPDDYPERLEHLAQIEACYSVAGDSSYLVRVRVASPKALEDLLRQIREVANVSTRTTVVLSTPYEDRPPAV
>NZ_CP023445.1|WP_096492775.1|2540126_2540873_-|class-IV-aminotransferase
MRRIEVDGVAATAQDMAGLFGNYGHFTAFQVRNGLVRGMDQHLDRLAEGNRELYSLDLDRDRVRALVARALRGVGDASVRVVLFGVDAPTTLVSVREPREPPELPQSLLPVEHVRPLPHVKHLGGFERAVHHRAAREAGFDGALLIGGGGLVVESAVANIGFLTGDEIVWADGPWLHGTTMRLLEEHAPSRRAPVRLADLGAHDGAFTANSWGVAPVHRIGDVRYPVGRAFERLRATFAAIPQHPVTP
>NZ_CP023445.1|WP_096492776.1|2541101_2542301_+|MFS-transporter
MATGFRAVFGVAEFRVLWCAAVLSTLGDQLARVALSVLVFERTNSAAWTALTYALTMLPALFSGVLFSGLADRYPRRTVMVVADLLRAVVLAVMALPGVPLPLVAALLVLAQLAEPPFAAAQGALLPAVLGDRYEAGQSVHLITHQAGLLLGFAGGGLAVHWLGTSGALAADAATFAISALLLRLGLEARPAPASARTTRLRINEGAALVWRTPRLRLLVLLGWLALFTVVPEGLAAPFSDEVGTGAAGVGVLLAADPAGMVLGTVLLRYLPTERRVRLLGLLAVATALPLVAYLLHPGLLGAVTLLALSGVFSAYQVTAGATFVRLVPDARRGQALGFARSGLVAAQGVGVAGGGLLATATGSAATAIAIAAGVGVLAAAAVTARWMALGPLEQLAEG
>NZ_CP023445.1|WP_096497735.1|2542665_2543892_+|GGDEF-domain-containing-protein
MGYVLSVDLLALLAVAAAATTRQPTTRHDWVVLAVLLACAALHLVFSRWIERARRDATGLPHLDLCSIWIFAGSLLLPPPLVGVLVVVLYAHRWWVVGRWDPFRPPHRGVFTAAMMLLVALAANVVATATGLRESLAAGHLEGPWDLLGLMGAGSVYWTVNTALVAGVIVLTTGARTHLFGGPLDNLLEAAQLSLAFFVALAVAWWPGFALPMVVAAVALHRTVLIHQLELAARTDAKTGLLNAEAWHLQARVELNRTRQRGDSLGLLMIDVDHFKGINDTHGHQTGDEVLRSIADVIRESVRRGDSVGRFGGEEFVVLLPGAGRDESMAIAERARCRVGLLGTGAGPVRGLTVSVGVAVWPDVPEDTVEGLLAAADGALYQAKRLGRDQSRAAWSHPVPSVRSDQGG
>NZ_CP023445.1|WP_157767592.1|2544056_2547404_+|hypothetical-protein
MDLGPPHGIRFRFSTGLVRAVLLDAHGKPPLPLAEALSIDVGTRELAVAEDHGDPLRAVLRQRYDLAEPVEWRLHVPGDASVDGDGVQFALPTGTSVRVTSTGQVSATEDGVVVALPAGPAEIDVEVVSEPQYAVSDTVVVCRAHQAREAAVVVSCLPGDRFTPVVALDRPPPAGGRHALPGEHDDELDAPGPDTGPLRSWNNRNSLLADLMRATGVRRAVVLADPPPQAAHVFDGMEHVRLLKPDLLGEDLTDEVWALLHGEGRQPAKVLEAAPGDDPAQALYTALRTGSALRFTERADPLGDRFAAAGPESGDEAVLVETTGEADDLVAACYAHHRGARLVTTPQPDLDEVGRVVAEEQARVTEAASAIGDAVKGIAVGEALWRYLSTGGHDPYPAVESVVTAQVPADAVHAVGERRLTAFTAGLPYPFVRTATGSWARKPIGHVTTDPALVVLTELHREGACRPRGAFALLVDPGFPAAPADRAAHVTHPVVLTGAETALPVVAALAADLPVEVLAVNAHDAEGNALLDGSPLPPWLVAHALDLPHQPVVLNNSCLSWTDQAREYLRVGARGYVGALWRIPPDLAADFTRVVVRRLTAGEVPAARAVVDTGLPGGIERSYLYAGTANGRLDRWRAGAPGEGESALTGCALLAGVDHGGEEVLRKVVHREMSALRRAAETTPASGTEAYVDTLFDELSFAGDLSDAAEVVEKIDKALPALDLPPAEADRRWAARYERTGALHEHGGDHGAALADYGRSASYGDAGPDRAGVLLRMAALEPRPEEALRLASQAYRAAVAAGDRDTEFHACSSLNDLGRRTGDLDTALKHAVIGHDLAAVRGDRVRQTAFKVDECALRRELGDPDGAIEAGTDALELVRAQGDPATELRVIGELARCHEARGDLAAALSYTKAGLSLSEHQDAPGEFARFQDETGRLLTRRGEHAEALRHYRSAVEGLVARGSLERGAELLPHLAVGAVRAGDAGALWTTALCGGLVCEVVERDVWQALVPLVVDSMKRAIEIGSAELTQRGMTDFASAVTAGRRDDMPVQVGVLSDVVVLLLAWLMGRIDDSMLAFGREVDRQTGGVLDLVGYVSTPYAQRVRGGAVAGRWSAR
>NZ_CP023445.1|WP_096492778.1|2547414_2548362_-|peptidase-S58-DmpA
MRNAITDVPGVLVGHVTRIGGGFLTGTTAVLLPPGNLVVADVRGGGPATVDTAAVDARYGGREVPGVVLTGGSAFGLAAARGAAAELGGGVVPGAALFDLGRGGDFGARPDASFGALAVRAASVEAPQGNVGAGTGALNVALKGGLGTASADLGGGVVVGAIAALNAVGPSYAPDGLPLAAGLGLPGEFPSAILDPAVAPAPPAPPPFNTVIGVVATNAAVPPFALAAAAQDGLALAVSPAHGTADGDTVFGAVTGARQAPPDEVLRAASRVFARALVHGLLAAEPVTTPRGRLTAHRELFPRTRAAHRAAHRGA
>NZ_CP023445.1|WP_096492779.1|2548372_2549911_-|aspartate-aminotransferase-family-protein
MDDRGRPEAPAPDLTSDNAAGKHAGGQDPFEQPPIPPDAAGRGPVDNAAAALELVARAAAPFLAGLDDRPVHPPGRDRLIDELTGPLPEDGDGALVAVAELLRVGTAAATATAGPRYFGYVVGGATPAAQAGDWVVSLLDQPAGLWPTSPLAAGAETVVLGWLKDLLGFPASHGGVLTPSATFANLTGLACARQWWAAEHGVDVAADGLAGLPRMPVLSSGYAHASCRKALQVLGCGRDGVRLVAHPDGSLDVDRLDRELADSGPSVLIGTAGEVDAGRYDPLDELADLAERHGAWLHVDGAFGLFAAASPRTRGLVRGVERADSVAADCHKWLNTPYESGFALVRDRSALGRAFGSWNAAYLPEPDDTRVDYNTLGPESSRRARALPLWAALRAYGRAGHRAVVERHLELARRLGGLVEAADDLELLSPVTLFVVCFRYRPAGVTDPARLDALNRSLGAALAEDGRVHAGTTVHRGSVALRPAIVNWRTRPEDVDLLVAVVRELGARVAAR
>NZ_CP023445.1|WP_096492780.1|2550085_2551771_-|DEAD/DEAH-box-helicase
MTDAPDDDRTSFADLGLRPELLRALSGLGYEEPTPIQREAIGPLTEGRDLLGQAATGTGKTAAFALPVLERLAQVEKRGDAPFALVLVPTRELAVQVSEAVHRYGRELNARVLPIYGGQPIGRQLRVLERGVDVVVATPGRAVDHLGRGTLNLEDLQVVVLDEADEMLDMGFAEDLDTILAETPKQRQTVLFSATMPPRIDKLARQHLTEPARITINQERAEPGEAPRVRQVAYVVPRAHKPAALGRVLDVEAPTAAIVFCRTRDEVDQLTETLNGRGYRAESLHGGISQEQRDRVMARLRNGTADLLVATDVAARGLDVEQLTHVVNYNVPSAPESYVHRIGRVGRAGREGVAITLAEPREHGMLKTIERVTKQRITMEKVPTVADLRARRLELTRAALHESLLEDDLERFRVVVESLSDEFDVMEVALAAVKLAHEASGAAADEEEIPEVAHRPDRGRGGAAGGDGQRRERRVRPPTAGMTRLFVGAGRSSGIRPQDIVGAIAGEARLQGRDIGAIEITDRFSLVEVPESSAQHVITALRGATMKGRKVTVRRERDAQR

Crispr_ID: NZ_CP023445_6

• CRISPR_ID: NZ_CP023445_6
• CRISPR_location: 2908156-2908244
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_6

Consensus_repeat	Method
CCGCCCCCGCTTCCACCCGCTCCGCCC	CRISPRCasFinder

spacers of NZ_CP023445_6

>6.1|2908183|35|NZ_CP023445|CRISPRCasFinder
CGCTTCCACCCGCTCCGCCCCCGCCTCCCCCTGCT

CRISPR arrays and Neighbor proteins around NZ_CP023445_6

CRISPR arrays

The CRISPR arrays of NZ_CP023445_6

>merge|NZ_CP023445|6|2908156-2908244|CRISPRCasFinder
CCGCCCCCGCTTCCACCCGCTCCGCCCCGCTTCCACCCGCTCCGCCCCCGCCTCCCCCTGCTCCGCCCCCGCTTCCACCCGCTCCGCCC

>NZ_CP023445|6|5|2908156-2908244|CRISPRCasFinder
CCGCCCCCGCTTCCACCCGCTCCGCCC	CGCTTCCACCCGCTCCGCCCCCGCCTCCCCCTGCT
CCGCCCCCGCTTCCACCCGCTCCGCCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_157767620.1|2911913_2912417_+|hypothetical-protein	unknown	unknown	gnl|CDD|379553
NZ_CP023445.1|WP_096493009.1|2907038_2908151_+|glycosyltransferase-family-1-protein	unknown	unknown	gnl|CDD|340817
NZ_CP023445.1|WP_096493007.1|2905433_2905931_+|SRPBCC-family-protein	unknown	unknown	gnl|CDD|176908
NZ_CP023445.1|WP_096493015.1|2919348_2920194_+|DUF3152-domain-containing-protein	unknown	unknown	gnl|CDD|371483
NZ_CP023445.1|WP_096493008.1|2906105_2907020_+|cytochrome-c-oxidase	unknown	unknown	gnl|CDD|224528
NZ_CP023445.1|WP_096493016.1|2920288_2922259_-|ricin-type-beta-trefoil-lectin-domain-protein	unknown	unknown	gnl|CDD|373145
NZ_CP023445.1|WP_096493013.1|2915791_2916730_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|235736
NZ_CP023445.1|WP_157767621.1|2913729_2914908_-|hypothetical-protein	unknown	unknown	gnl|CDD|214672
NZ_CP023445.1|WP_096493014.1|2918600_2919269_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP023445.1|WP_096493005.1|2903185_2903785_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096493002.1|2897298_2898417_+|hypothetical-protein	unknown	unknown	gnl|CDD|365866
NZ_CP023445.1|WP_096493000.1|2895373_2896228_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096493006.1|2903899_2905333_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP023445.1|WP_157767619.1|2908663_2910820_+|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|236645
NZ_CP023445.1|WP_096497758.1|2915127_2915688_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_CP023445.1|WP_096493004.1|2901941_2902898_-|nitroreductase	unknown	unknown	gnl|CDD|236122
NZ_CP023445.1|WP_096497759.1|2916751_2918530_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|223715
NZ_CP023445.1|WP_096493017.1|2923274_2925827_+|hypothetical-protein	unknown	unknown	gnl|CDD|379075
NZ_CP023445.1|WP_096493001.1|2896292_2897105_-|hypothetical-protein	unknown	unknown	gnl|CDD|225148
NZ_CP023445.1|WP_096493003.1|2898490_2901577_-|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl|CDD|223911

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_157767620.1|2911913_2912417_+|hypothetical-protein	gnl|CDD|379553	pfam14317, YcxB, YcxB-like protein. The YcxB-like protein family includes the B. subtilis YcxB protein, which is a functionally uncharacterized transmembrane protein. This family of proteins is found in bacteria, and is approximately 60 amino acids in length.	1.56407e-10
NZ_CP023445.1|WP_096493009.1|2907038_2908151_+|glycosyltransferase-family-1-protein	gnl|CDD|340817	cd03784, GT1_Gtf-like, UDP-glycosyltransferases and similar proteins. This family includes the Gtfs, a group of homologous glycosyltransferases involved in the final stages of the biosynthesis of antibiotics vancomycin and related chloroeremomycin. Gtfs transfer sugar moieties from an activated NDP-sugar donor to the oxidatively cross-linked heptapeptide core of vancomycin group antibiotics. The core structure is important for the bioactivity of the antibiotics.	1.39273e-53
NZ_CP023445.1|WP_096493007.1|2905433_2905931_+|SRPBCC-family-protein	gnl|CDD|176908	cd08899, SRPBCC_CalC_Aha1-like_6, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	5.43114e-35
NZ_CP023445.1|WP_096493015.1|2919348_2920194_+|DUF3152-domain-containing-protein	gnl|CDD|371483	pfam11350, DUF3152, Protein of unknown function (DUF3152). Some members in this family of proteins are annotated as membrane proteins however this cannot be confirmed. Currently there is no known function.	3.17666e-82
NZ_CP023445.1|WP_096493008.1|2906105_2907020_+|cytochrome-c-oxidase	gnl|CDD|224528	COG1612, CtaA, Uncharacterized protein required for cytochrome oxidase assembly [Posttranslational modification, protein turnover, chaperones].	7.77966e-31
NZ_CP023445.1|WP_096493013.1|2915791_2916730_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|235736	PRK06196, PRK06196, oxidoreductase; Provisional.	6.31327e-113
NZ_CP023445.1|WP_096493014.1|2918600_2919269_-|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].	4.80797e-80
NZ_CP023445.1|WP_157767621.1|2913729_2914908_-|hypothetical-protein	gnl|CDD|214672	smart00458, RICIN, Ricin-type beta-trefoil. Carbohydrate-binding domain formed from presumed gene triplication.	5.97483e-14
NZ_CP023445.1|WP_096493002.1|2897298_2898417_+|hypothetical-protein	gnl|CDD|365866	pfam00089, Trypsin, Trypsin.	0.00788622
NZ_CP023445.1|WP_096493016.1|2920288_2922259_-|ricin-type-beta-trefoil-lectin-domain-protein	gnl|CDD|373145	pfam14587, Glyco_hydr_30_2, O-Glycosyl hydrolase family 30.	6.66137e-17
NZ_CP023445.1|WP_096493006.1|2903899_2905333_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.01793e-54
NZ_CP023445.1|WP_157767619.1|2908663_2910820_+|EAL-domain-containing-protein	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	1.28077e-104
NZ_CP023445.1|WP_096497758.1|2915127_2915688_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	9.92205e-08
NZ_CP023445.1|WP_096493004.1|2901941_2902898_-|nitroreductase	gnl|CDD|236122	PRK07877, PRK07877, Rv1355c family protein.	1.75566e-24
NZ_CP023445.1|WP_096497759.1|2916751_2918530_-|HAMP-domain-containing-protein	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.07858e-69
NZ_CP023445.1|WP_096493017.1|2923274_2925827_+|hypothetical-protein	gnl|CDD|379075	pfam13208, TerB_N, TerB N-terminal domain. The TerB_N domain is found N-terminal to TerB, and TerB_C containing proteins. It has a predominantly alpha-helical structure and contains an absolutely conserved glutamate. The presence of a conserved acidic residue suggests that it might chelate metal like TerB. These proteins occur in a two-gene operon containing an AAA+ ATPase and SF-II DNA helicase suggesting a role in stress-response or phage defense.	4.38121e-50
NZ_CP023445.1|WP_096493001.1|2896292_2897105_-|hypothetical-protein	gnl|CDD|225148	COG2239, MgtE, Mg/Co/Ni transporter MgtE (contains CBS domain) [Inorganic ion transport and metabolism].	0.00126514
NZ_CP023445.1|WP_096493003.1|2898490_2901577_-|efflux-RND-transporter-permease-subunit	gnl|CDD|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0

Protein sequences

>NZ_CP023445.1|WP_096493009.1|2907038_2908151_+|glycosyltransferase-family-1-protein
MRVLFTSVGGLGHVLPLVPAAEAVRAAGHVVAFGCSSVQRRAVEAAGFEAFDLGGSTAAPPRTPLLAPDRAREDRDLREGFARREAGRRAPLCLELLGAWRPDVVVCEEVDFGGVVAAERAGVPHVNAQVIASGAFVRPEVVGEPLAALRQEHGLPPDPDLLMLRRNLLLSPFPPSFRDPAFPLPPTAFPLRPAVGPVGRGRGARTTVHFTLGTVFNSESGDLFARVLEGLSGLPVDVVATVGEHVDPAEFRVGERVRVERYLPQARVLPGCDVVVSHGGSGSVMGALGHGLPLVLLPMGADQPHNAERCARLGVGVELDPVAVTPEGVREAVAEVLAGPHREAALALREEMLGLPEPAAVVPLLEALAR
>NZ_CP023445.1|WP_096493008.1|2906105_2907020_+|cytochrome-c-oxidase
MQPTWKQRIVRSHRGLAIAAVVANVVIAGTGSTVRVTGSGLGCTEWPHCLPGSLVPVEHPELAMLTQWIEYGNRLLAVVVGVIGVLCLLAAWWSRPLRTRVLLLSAVMTGGVFAQAVIGGITVNLGLLWWTVAFHFVVSPVLAWYAVLLWRSLDEEDGPARPIAGALAQRLLVAAVVVLAALVVVGTMVTGAGPHAGDADVARFDAPVETLAQAHSVLLYLFLAVLAALGRSLRGAGVRKPYLVLLVAVLLQGAVGFAQYLTGVPAVLVVVHVLGSMAVVVAMANLWTACRVREPATDRVVLAA
>NZ_CP023445.1|WP_096493007.1|2905433_2905931_+|SRPBCC-family-protein
MPPTATGTLAETPGGVDLVLTRTFRADAEDVWAFLTESDRTARWFGPWEGEGRAGGTVRVRLEFEDGRPTCDLKVEACEAPGRLVLTMLGTGATWPIELLVVPGEAGETELRLVHHLGDDSGIGEIGPGWEYYLDLLVAAREGAEVPSFEDYYPALKPHFDALKR
>NZ_CP023445.1|WP_096493006.1|2903899_2905333_+|MFS-transporter
MTEPDPRRWKALAVSLVAGFMSLLDVSIVSVALPSMQRGLGTSPAGVQWVVSGYALAFGLVLVTAGRLGDAYGRRRVFLLALAGFIAFSALAGLAPTTEVLVVARLLQGAAAGALAPQNSALIQQLFRGAERARAFGFFGAVVGISTAVGPVAGGAILAAAGEDDGWRWVFYVNVPIGLVALVLAARLLPRAGVGERGRLDLLGVLLLGAGVLAVLLPLVLAESGGLTALWWLFPLGAALLAAFVVWERRTAARGGDPLLDVTLLTAVPGYASGLLLGTCYFVGFSGIWLVFALFFQTGLGYTPLQSGLAVTPFAVGSAASALVGGRLVSRWGRKLTVLGLALVVAGLVATGLLLRLAPPHLAGWWAAGALLVGGVGGGWVISPNTTLTLRNVPVRMAGAAGGALQTGQRIGAAIGSAALAGLFYLVLADTGQDYGAAVSLAIWAAAGAVVVALGVAVWELRAVGQPERGRNFAAAD
>NZ_CP023445.1|WP_096493005.1|2903185_2903785_+|hypothetical-protein
MNTEQMTRPQDQAATAGTETGTAGTETATAAETAGAATTTAAAEQGRDGWGAPEVGAAQVQAAGEPTWGAMPPAPSQPVASKRPAWLRGRNALVAGALGIAVAAGLGGFGIGLAVGDGGAGAGQQAPSGQFPGDGQFPGAGDGQTGGGQFPGMGDGQTGTGQFPGGRTGRGGQQTTPGTGSGSTPDTDSDTGSGTGSTT
>NZ_CP023445.1|WP_096493004.1|2901941_2902898_-|nitroreductase
MALGLTNDEVTAALEAASLAPSVHNTQPWLFRVAEDRIELHADTSRALRATDPEDRELRLSCGAALLNLRVALEGAGVRTAVTVARGTGSGALAVLRRVGGAAEPEPALVAAIPRRRTNRRPFRADPVPLGFRVALVRAAERERSWLHVVTDREERARLRGMVAQAHRELDADPRVRAELRRWTGLRVGADGVPTRAAGPRPAAGDEWATRDFLARGLPERVGAAGSGGGDLVAVLCSYHDGPAAEVQAGQAMQRVLLTATSLGLSASFLSQPVEVPAIREEVRLLAGGPFPQTVLRLGFGEPVPPTPRRSVADLLLG
>NZ_CP023445.1|WP_096493003.1|2898490_2901577_-|efflux-RND-transporter-permease-subunit
MSVLARLSLANRGLVALLSLVVLGFGVLALPSLKQQLFPSIELPAAAVVAPYPGASPDLVDSQVAEPIAAAARGVDGVEQVLTRSAESSATVQVMFTYGTDLNTAISQLQQAVNRLGSRLPEGVDPTIVQGSTDDLPVIALAATAGDDDIAMAAKLREQVVPELEAVPGVREATVSGERERQVTVTVDYAKLAAARLEPTALSAALTSAGMTIPAGSVTDGDRSLTVQVGGPVTSIEQLRAVRVNQQVTLGDVATVESAPLPATSITRTDGQPTLGISLTMGSDGNAVQISDEVRAKLGELGSAVGSTLTVSFDQGPAVAKAISGLTTEGLLGLLFAVVVILLFLMSLRSTLVTAVSIPLSVVVALVALWVGDLSLNLLTLGALTIAIGRVVDDSIVVLENIQRHLGYGEEKQKAVLEGTREVAGAVTASTLTTVAVFLPIAFVTGIAGELFSPFAITVTVSLLASLLVSLTIVPVMAFWFLKRPDVPTDPAEAEAARAAALEKEESSRLQRAYVPVLRFATKRRGVTVAASVLIFAVTLGLAGTLQTNFIGDTGGDALQGTQELEPGASLAARDEAAKKVEQVLADTDEVETYQVTLGGGGMLAGFGMGGSSTQISATLREGSDMEAVRERLTERLADVEGAGKVDFSAGAAAGFSSDGIEVLVTAPDAERLKQAADAVQRELTGAPGVGEVDNDLAVSAPRVQVAVREEAARATGLSNQVVGQFAMQALRGTPAGELPIDGATQQIVLRSGVAPTDVAALRELQLPGGVRLGQVADVSVVDGPVQIRRTDGDRSATVTAKATGSDLGTVTTEVTNRVNAVELPEGAETSIGGVSADQAETFADLGLAMLAAIAIVFLIMVATFHSVVQPLILLVSIPFAATGAIGLLLLTGTPLGLPSLIGMLMLVGIVVTNAIVLIDLVNQYRAAGMGVVEAVVEGGRRRLRPILMTAAATIFALLPMALGITGEGAFIGKPLAIVVIGGLLSSTLLTLVLVPTLYTIVENRKERRAARRAAKRSEQPERETASV
>NZ_CP023445.1|WP_096493002.1|2897298_2898417_+|hypothetical-protein
MRTARSALALVAVVAASTALGTAPAALAGTGTGDWDRMLAQQPLVAAADVIKAEVDRGGHADGFAGIALEDDHVALWWKGAPPAAVTEAVARASAEAPVRVERAAHSEAELRAAAKDLEARRGPGSAVHSIKVPADGSGLVLGTRSDAVARSLATTADVPVRTVVEEPLVPVSRQNDSPPWKGGATIVLNNSAACTSGFSVRNGDNARFLLTAAHCGQSGVRVTDPTGEHIGNAGARHGDHDIMLIPTGNVVNRQYVGGGDSNSTEVVRGWGDVYVGEYLCQSGVTSARETGSQVCNIKVLFFYADREDLVEGEQVDGRPAARPGDSGGPVYGPSSDGGVIAKGTVTRTAGARIGFQDFRTASRDFGVYIPL
>NZ_CP023445.1|WP_096493001.1|2896292_2897105_-|hypothetical-protein
MGRSSDDDDQTYRVHNVVRGDVSGPVVQAGRIEGGLTLHGGGLQPPPRPRRLVEPHEVLDLPDAEARRALLDNRDRTFLARAADHDPDRTVELLASLGDDQRDSVLRRTRDLPGWLTELTAALADLEAVARTWRGYLGAPVDLVHREGPSPHGTTGYGLRFERGAALWCADSGPRVLMEGVHALHRAQGGASGWLGFPLADELSVTSPHGTDGCAQRFQGGTAYQAGDRAFAVRDTTGALFERYGFPLGSPLRDGSGWVQEFEGGRVRQH
>NZ_CP023445.1|WP_096493000.1|2895373_2896228_-|hypothetical-protein
MDGQQGGRNAFENSSAENVVQAGIVNGDVHVNTAKPPLANLSPRAAAAHLATMDFSAATDALAAAPERGKLVAALLEDHEATLVALLADMQRTVARELVHSLPSPPKWLRELLTAAEGFANMALGPARKKVRRADPSPQGSTGFSRDYDLGRAYWSANTQFYSVAHPVLGVHDRRGGTGGDLGFPIGERSWRYTPSTTKGLFYQEFEGGVVYESAPPMVVRDPDGALFERFGFPTGEETALGTFFADDVKGTFQPFERGTAYWVDNVALVREGESSAMFGVRKP
>NZ_CP023445.1|WP_157767619.1|2908663_2910820_+|EAL-domain-containing-protein
MAADVPPASGSAHRTGRRTLHRIRVLTTVFAWLSGVLTIGSLVATGEGPLPIGVAALVAGVLACWLRVPRDAWWIPPLEGVVAFASLLLLPDPQVVVGFVIGATVRRALYPEDAGFWSKSAVLVGSYLTGLAASLLWGWGVIRPELLPTLLMPLAGMAVAAAALHEAARAVLRAESAQRGAEHARATATAVLQASPVGLVLLDSGGAPVLHNERAQFLLDWAGQNGAAVPCPHGPNIAVCERGCRDADAEPVEVWVADRDRVLALHPVRVEQAGDEDRTLVAAVDISVRRRLEDELRHRSERDVLTGLTSRSHFLHLLDRALRAGDVGLLVLDLDQFKEVNDTEGHDAGDQYLVAASRRIRAAVEPDAVAARLGGDEFAVLAPGLDEQACGQLAKSVLAELEKPWSDLGYDVRMQASIGVAVSSAAAGVVGTAELLRDADTAMYVAKREGGARARCFRREMGEQALARQRDKLDLRAAIGTDQLVLHYQPIVDLATTAISGAEALVRWERPGRGLLGPGEFIGLAEQTGLIVPLGSSVLTSACTQAAGWRAAGRELGVTVNVSTRQLSAPGFLAALAKSLDVSGLQASALTIEVTESVWADEAAMRALMAVRETGVRVALDDFGTGYSSLSYLHRYPFDVVKIDKSFTWALGDTGRTAGVVRCIIDLADVLGAVTVAEGIETPEQAEWLRRAGCGYGQGFLFGRPDLPRNLALPQVGR
>NZ_CP023445.1|WP_157767620.1|2911913_2912417_+|hypothetical-protein
MTITVPYDERLFKRTTQFLLRPQLNRLYVLGAVLVALGVAMLTLTTIDKVVGVVCVVLGPLLVFRIGRVTAAQALEAQWSATRAAFNLVIDDQWVSIAYPLAQMRCHWETVARVVEKPDVWYLMFTKSQAVPLPKNLMTPEQQAEFAALAAARTSVVPLRRASAQRA
>NZ_CP023445.1|WP_157767621.1|2913729_2914908_-|hypothetical-protein
MRRWRAAWSAVAAAALVGTGAAAGPAHAQDAGEIAGTVWVDKDQDRQPGEHEARRAGVTVTALQRATGERRTTRTDERGDFRFTGLPLGSYQVEADRTGYAALADRTWDVELTSGSPRAGQAWFPQQGGTLGGQVSVDADDDGARDASPERVAVTVHLWGRDLTGAEVRASTTTSDYGWYHFDALATGAYQVRAEVPQGYRLARPNAGAGSSGAHTDFDLLGADATSLPVRFAETGSRYAAVDIGLVRGEGVAPEPVLVNAASGWCADQELPGGAVTTGVAAGDCHGGDNQRWRARWVEPDVAEFVDARTGFCLDQEFPGGRRTSGVGAYRCHGGANQRWRVSHDEQGGEPFTAVNLATGECLDQEYPTGTPTTGVGAYQCHGGANQSWVAR
>NZ_CP023445.1|WP_096497758.1|2915127_2915688_-|TetR/AcrR-family-transcriptional-regulator
MTDPDQRPLRADAQRNRDKLLAAALAAFTERADAPLEGIAKQAGVGIGTLYRHFPTREALIEQVYRAELDRLCDAAPHLLTTSPPEVALRRWMDLFLEYLDTKRGLADALRAVITGAETPFPHARKRLLEALGVLVDAAVRTGALRDDVPALDVLVGMAGIANATDDAAQAGRLLDLLVAGLRAGR
>NZ_CP023445.1|WP_096493013.1|2915791_2916730_+|SDR-family-NAD(P)-dependent-oxidoreductase
MTANTAPRFTASSTAAEVVAGIDLTGKRAVVTGAASGIGVETARALASAGAQVTLAVRDRAAGERAAADITATTGSTAVRVAPLDLADQVSVAAFTANWDDPLHLLVNNAAVMACPLARTPEGWELQFATNHLGHFALTKGLHRHLAAAGGARVVSVSSSAHHRSPVVFDDVHCTEREYQAWDAYAQSKTANVLFGVSATTRWAADGITVNALMPGSISTNLQRHVDLEEIARARAAAGVTEVRRKSPEQGAATSVYVATAPELEGLGGKYFEDCAEAGPFVPGTNRGVADHALDPEAADRLWEVSLRTLAG
>NZ_CP023445.1|WP_096497759.1|2916751_2918530_-|HAMP-domain-containing-protein
MSALIAACSIAVTAWLASQATTGAIRQEQGEALAVDARIYDELLGFAATHPDWSGVQSTVDRLAVETGRRVALTTPGRAVLADSGGPGAPELPVNARVQVDPLTVNAVLKPGGGEVDPRAVGPFALDGGSLAELESRLARVRQCAAVVVRRLPGERPWVAESTAPAWTTAPDGNGRDGGQRCDALWVNAPLEVEWPALVDLEGRTAACLARTSPPSAAPSPSTPVSPPVSLRALAKRDAGWYLRDEVTGDPELAACALAARREQLASHVAQPALLFLTAPTGGEPRPIDLSTAGATRIALTGAGILVVAGLASWGTATAVVRPVRALTAAARRMTGGDRSVRVREPSGEVGELAGAFNALSERLAEVERQRRAMVSDVAHELRTPLANITGWLEATQDGLAEPDPALIAMLLEEAFLLQHMVDDLRDLAQADAGALRLHREPVDVVELVAQTAAAHRVSARAQGVRLEVACAGELVLHGDPVRLRQVLANLVGNAVRHTPSGGSVVVRGRGGGGVVVLEVVDTGEGLAPEDLARVFDRFWRADPSRNRATGGSGLGLAISRHLVELHGGSVVAESEPGVGSVFRVVLPAGDA
>NZ_CP023445.1|WP_096493014.1|2918600_2919269_-|response-regulator-transcription-factor
MRARILLAEDNPHQAELVRRYLEHDGHDVTVVGDGRAAIDEARRSAPDLLVLDVMMPGVDGLDVCRVLRAESDVPIVLLTARALEEDVLLGFDLGADDYVVKPFRPRQLVARVRTILRRAGRSAGPAPSPVLRVGDLVVDPVRHEVNLAGAQVPLTPAEFRLLSVLAAQPGRVFTRAQLLDDGFITARTVDVHVMKLRRKVERDPRAPERLLTVYGVGYKLV
>NZ_CP023445.1|WP_096493015.1|2919348_2920194_+|DUF3152-domain-containing-protein
MKVTPALLACLATAVVFTAAGVVTPPEEPPTGPVAEAEPQEPAAPAAAVADPAEPERVAAEPMAADSEPEPRRVYERSSDLPDGGPFAERGSGTWHVVPGTFAEAGSGAALSYTVEVEDGVQVDEHAFAGFVQQTLADPRGWISAGFALRRVDSGVPDFRVRLTSQATARERCGFQIPVDVSCRDGGAVDLSAARWARGAVAYLGDLDGYRRYVVNHEVGHALGRGHVPCAEHGAPAPVMMQQTFSTSNDEINLITAGSAQGGVVPNDGKVCAPNPWPFPG
>NZ_CP023445.1|WP_096493016.1|2920288_2922259_-|ricin-type-beta-trefoil-lectin-domain-protein
MKARAALAAIVVASAALSPVGAAQAQAQQADVTVRPDPTYRQEPFQGWGTSLVWFANATGQYPNSVRNELADLLFSAQGLNLNIARYNIGGGNAPDVPPYLRAGGAVPGWWKAPEGTTRTDTDWWEPNNPELFDAEADPGQRWWVDKIKSKVDRWEAFSNSPPWFQTVSGYVSGGFDANADQLRADKIDEFTAYLAQVVEEMEDAHGIEFDTVDPFNEPNTNYWSTRLGADGNPTGGRQEGAHMSPALQAKVIPSMVKALRDKGLSAAVSAPDETNPGTFAADWAGYPAAVRAQVGQLNVHTYGTGQRTSARDIAKGADKPLWMSEVDGSWGSGQSFTSMDPGIGIAERVVDDLRELEPRSWVLWQAIEDYDNMKPGGESPQGANWGVVQVPFSCTTSDCEVRTNTKFDTLRNFTHHIKPGDRVIGVNTTTDVVAMRGESLKTVVHVNKAEQARTVALDLRSFKRISKSAKVQPVVTDASGALVEGAEVAVRDGVATLTVPARSVTTFRVSGVSGAIGAEALGAREAYRLTGVQSGKSLAPNGTALVQRNSAEVADQYWELERLDDGFGNRVRFAVVNAGTGQRLAAVGGEAVLRSADGPEARWIASSTGDGTWTLVNAATGAMLDVVGQSTADGAKVGLYTPTSGPNQRWTATPR
>NZ_CP023445.1|WP_096493017.1|2923274_2925827_+|hypothetical-protein
MGLADRLRRALGLPDPEEPEHELEPVRTPGGPTGSPEPAEHAPAEHAPAEPRTEDRQPAAQRPVEPRPAARQPVEPPPVEPRPEDDPEHFASATGTFEPADTATLLPPDDPATEDPPADEPPPADRVRPFVPAVVPEPAAEAQRPPEDPAEPSFWLPEGVAVHFAGHTLEGGLLYLGRAGAPGTAHVIDPTLPVDPSADPTLPVDPSAEPTDRDPAPAYHAMSPRDRAAHLRWLATGRRDRTVPVGHVFLFLAGLEHRVVADRARADLPAVRAELRDLRARYGRHRPFHGAATALLDLVDVLLDDRPLPDPARWDRPDPPLALRVALGELAAAGQPVPAEWAHAWALLHPALDAPRARARFRELFTARYRERHGDGLLINPAAPPLTVRYRPTAEGVPPAEVPTDLPDVLTTPASTRALAELLDTCADELHAHDGLLADDPAAEGTAPALALLPRCVVTGGEPALDPFRALVDRVLPDGAALGVFELADLVALWPGGFDGAGAIGAARLLGHLGVGLEPDARTGLEEPRASGPAALFRVADAEDLPHAATPEYRAASTLLRLAASGEGLSEPERVDLTAHLGSALRLTDGEVARLNAHAVLLLTPGAPPAPQRLSGLTLGQRVHIADLASAAARVDTAPPGVDQVFRRMRAALDPSDPIPELPPAPEPALEAPQEPEAPPEPEVIATIVPASAEVPALLELTTVDLTTAPEPPALPAAPSPPAADSQATDSPVPDPRPADPTPADPTTSHLLATLAEDDPTTPSPRRAVLPVDLVPGLDAGHSALLRELAARPLWPRAEFDRRCAALHLLPIGALDALNEAAVAACGEPLAEPGEHGLLVNDTALGELLA

Crispr_ID: NZ_CP023445_7

• CRISPR_ID: NZ_CP023445_7
• CRISPR_location: 3788681-3788773
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_7

Consensus_repeat	Method
CGGCCCGGTCCAGCAGCGCCCGT	CRISPRCasFinder

spacers of NZ_CP023445_7

>7.1|3788704|47|NZ_CP023445|CRISPRCasFinder
CCCCCAGCCAGCCCTCGCCCGCCAACCAACACCTACCCGTCAACCCC

CRISPR arrays and Neighbor proteins around NZ_CP023445_7

CRISPR arrays

The CRISPR arrays of NZ_CP023445_7

>merge|NZ_CP023445|7|3788681-3788773|CRISPRCasFinder
CGGCCCGGTCCAGCAGCGCCCGTCCCCCAGCCAGCCCTCGCCCGCCAACCAACACCTACCCGTCAACCCCCGACCCGGTCCAGCAGCGCCCGT

>NZ_CP023445|7|6|3788681-3788773|CRISPRCasFinder
CGGCCCGGTCCAGCAGCGCCCGT	CCCCCAGCCAGCCCTCGCCCGCCAACCAACACCTACCCGTCAACCCC
CGACCCGGTCCAGCAGCGCCCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096494008.1|3815575_3815818_-|acyl-carrier-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096493985.1|3779607_3780270_+|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|366722
NZ_CP023445.1|WP_096494006.1|3814271_3815480_+|glycosyltransferase-family-1-protein	unknown	unknown	gnl|CDD|340817
NZ_CP023445.1|WP_096493987.1|3780351_3783189_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|276938
NZ_CP023445.1|WP_096494015.1|3818416_3821434_+|cytochrome-P450	unknown	unknown	gnl|CDD|99802
NZ_CP023445.1|WP_096494018.1|3823211_3823784_-|deaminase	unknown	unknown	gnl|CDD|223340
NZ_CP023445.1|WP_096494002.1|3789396_3790563_+|DegT/DnrJ/EryC1/StrS-family-aminotransferase	unknown	unknown	gnl|CDD|366433
NZ_CP023445.1|WP_096494012.1|3817077_3817542_-|DUF4383-domain-containing-protein	unknown	unknown	gnl|CDD|379556
NZ_CP023445.1|WP_096494017.1|3821473_3822520_-|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|235640
NZ_CP023445.1|WP_157767680.1|3822879_3823227_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096494010.1|3815997_3817023_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|187618
NZ_CP023445.1|WP_096493981.1|3777105_3778221_+|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|173838
NZ_CP023445.1|WP_096493983.1|3778217_3779615_+|HAD-IIIC-family-phosphatase	unknown	unknown	gnl|CDD|273757
NZ_CP023445.1|WP_096497817.1|3787578_3788478_+|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_CP023445.1|WP_096493979.1|3776840_3777113_+|acyl-carrier-protein	unknown	unknown	gnl|CDD|223314
NZ_CP023445.1|WP_096493996.1|3787117_3787483_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096493992.1|3784364_3784712_-|hypothetical-protein	unknown	unknown	gnl|CDD|226318
NZ_CP023445.1|WP_096493994.1|3784927_3786940_+|carbamoyltransferase	unknown	unknown	gnl|CDD|225103
NZ_CP023445.1|WP_096493989.1|3783214_3784351_+|acyltransferase	unknown	unknown	gnl|CDD|224748
NZ_CP023445.1|WP_096494004.1|3790893_3804948_+|type-I-polyketide-synthase	unknown	unknown	gnl|CDD|225858

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096493985.1|3779607_3780270_+|SAM-dependent-methyltransferase	gnl|CDD|366722	pfam01596, Methyltransf_3, O-methyltransferase. Members of this family are O-methyltransferases. The family includes catechol o-methyltransferase, caffeoyl-CoA O-methyltransferase and a family of bacterial O-methyltransferases that may be involved in antibiotic production.	4.89353e-65
NZ_CP023445.1|WP_096494006.1|3814271_3815480_+|glycosyltransferase-family-1-protein	gnl|CDD|340817	cd03784, GT1_Gtf-like, UDP-glycosyltransferases and similar proteins. This family includes the Gtfs, a group of homologous glycosyltransferases involved in the final stages of the biosynthesis of antibiotics vancomycin and related chloroeremomycin. Gtfs transfer sugar moieties from an activated NDP-sugar donor to the oxidatively cross-linked heptapeptide core of vancomycin group antibiotics. The core structure is important for the bioactivity of the antibiotics.	6.16996e-42
NZ_CP023445.1|WP_096493987.1|3780351_3783189_+|AAA-family-ATPase	gnl|CDD|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	1.69337e-49
NZ_CP023445.1|WP_096494015.1|3818416_3821434_+|cytochrome-P450	gnl|CDD|99802	cd06206, bifunctional_CYPOR, These bifunctional proteins fuse N-terminal cytochrome p450 with a cytochrome p450 reductase (CYPOR). NADPH cytochrome p450 reductase serves as an electron donor in several oxygenase systems and is a component of nitric oxide synthases and methionine synthase reductases. CYPOR transfers two electrons from NADPH to the heme of cytochrome p450 via FAD and FMN. 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.	3.0943e-138
NZ_CP023445.1|WP_096494018.1|3823211_3823784_-|deaminase	gnl|CDD|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	8.86099e-18
NZ_CP023445.1|WP_096494002.1|3789396_3790563_+|DegT/DnrJ/EryC1/StrS-family-aminotransferase	gnl|CDD|366433	pfam01041, DegT_DnrJ_EryC1, DegT/DnrJ/EryC1/StrS aminotransferase family. The members of this family are probably all pyridoxal-phosphate-dependent aminotransferase enzymes with a variety of molecular functions. The family includes StsA, StsC and StsS. The aminotransferase activity was demonstrated for purified StsC protein as the L-glutamine:scyllo-inosose aminotransferase EC:2.6.1.50, which catalyzes the first amino transfer in the biosynthesis of the streptidine subunit of streptomycin.	2.78857e-133
NZ_CP023445.1|WP_096494012.1|3817077_3817542_-|DUF4383-domain-containing-protein	gnl|CDD|379556	pfam14325, DUF4383, Domain of unknown function (DUF4383). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 137 and 164 amino acids in length.	2.08521e-41
NZ_CP023445.1|WP_096494017.1|3821473_3822520_-|RNA-polymerase-sigma-factor	gnl|CDD|235640	PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.	6.00531e-179
NZ_CP023445.1|WP_096494010.1|3815997_3817023_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|187618	cd05360, SDR_c3, classical (c) SDR, subgroup 3. These proteins are members of the classical SDR family, with a canonical active site triad (and also active site Asn) and a typical Gly-rich NAD-binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	2.47136e-111
NZ_CP023445.1|WP_096493981.1|3777105_3778221_+|acyl-CoA-dehydrogenase-family-protein	gnl|CDD|173838	cd00567, ACAD, Acyl-CoA dehydrogenase. Both mitochondrial acyl-CoA dehydrogenases (ACAD) and peroxisomal acyl-CoA oxidases (AXO) catalyze the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of ACAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. In contrast, AXO catalyzes a different oxidative half-reaction, in which the reduced FAD is reoxidized by molecular oxygen. The ACAD family includes the eukaryotic beta-oxidation enzymes, short (SCAD), medium (MCAD), long (LCAD) and very-long (VLCAD) chain acyl-CoA dehydrogenases. These enzymes all share high sequence similarity, but differ in their substrate specificities. The ACAD family also includes amino acid catabolism enzymes such as Isovaleryl-CoA dehydrogenase (IVD), short/branched chain acyl-CoA dehydrogenases(SBCAD), Isobutyryl-CoA dehydrogenase (IBDH), glutaryl-CoA deydrogenase (GCD) and Crotonobetainyl-CoA dehydrogenase. The mitochondrial ACAD's are generally homotetramers, except for VLCAD, which is a homodimer. Related enzymes include the SOS adaptive reponse proten aidB, Naphthocyclinone hydroxylase (NcnH), and and Dibenzothiophene (DBT) desulfurization enzyme C (DszC).	2.2353e-59
NZ_CP023445.1|WP_096493983.1|3778217_3779615_+|HAD-IIIC-family-phosphatase	gnl|CDD|273757	TIGR01686, modular_polyketide_synthase, FkbH-like domain. This model describes a domain of a family of proteins of unknown overall function. One of these, however, is a modular polyketide synthase 4800 amino acids in length from Streptomyces avermilitis in which this domain is the C-terminal segment. By contrast, the FkbH protein from Streptomyces hygroscopicus aparently contains only this domain. The remaining members of the family all contain an additional N-terminal domain of between 200 and 275 amino acids which show less than 20% identity to one another. It seems likely then that these proteins are involved in disparate functions, probably the biosynthesis of different natural products. For instance, the FkbH gene is found in a gene cluster believed to be responsible for the biosynthesis of unususal "PKS extender units" in the ascomycin pathway. This domain is composed of two parts, the first of which is a member of subfamily IIIC (TIGR01681) of the haloacid dehalogenase (HAD) superfamily of aspartate-nucleophile hydrolases. All of the characterized enzymes within subfamily III are phosphatases, and all of the active site residues characteristic of HAD-superfamily phosphatases are present in this domain. The C-terminal portion of this domain is unique to this family (by BLAST).	1.55711e-97
NZ_CP023445.1|WP_096497817.1|3787578_3788478_+|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.287e-31
NZ_CP023445.1|WP_096493979.1|3776840_3777113_+|acyl-carrier-protein	gnl|CDD|223314	COG0236, AcpP, Acyl carrier protein [Lipid metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	3.34419e-07
NZ_CP023445.1|WP_096493992.1|3784364_3784712_-|hypothetical-protein	gnl|CDD|226318	COG3795, COG3795, Uncharacterized protein conserved in bacteria [Function unknown].	3.40044e-14
NZ_CP023445.1|WP_096493994.1|3784927_3786940_+|carbamoyltransferase	gnl|CDD|225103	COG2192, COG2192, Predicted carbamoyl transferase, NodU family [Posttranslational modification, protein turnover, chaperones].	7.41226e-164
NZ_CP023445.1|WP_096493989.1|3783214_3784351_+|acyltransferase	gnl|CDD|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	1.50961e-27
NZ_CP023445.1|WP_096494004.1|3790893_3804948_+|type-I-polyketide-synthase	gnl|CDD|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0

Protein sequences

>NZ_CP023445.1|WP_096497817.1|3787578_3788478_+|ROK-family-protein
MSGSGTGGVVGVDLGGTKAAVRVVGADGRSGDSVVRWESGASAGEDLALLVRAVERAGGGGGVRSVGVAVPATLDRSGVVVAWPGRPGWVGVDVLGALGAMFPGASVRHGDDGDLAALAEADAAGCGELLYVGVGTGVGGGIVSGGLPLNSGGSCEVGHVVVERGGGLCDCGRRGCVQAFASGPAILRGAVARGGRPGGLGDVRDGVARGERWAVEACEDAASALAALVIGVGELVRPELALIGGGVTTALPGLVPAVAERVAGLGRTGHPVPSVRPAVLGAESSLHGALVLARGGNRE
>NZ_CP023445.1|WP_096493996.1|3787117_3787483_+|hypothetical-protein
MAAEVLGPVLAKAEVERIVARLALVGEGRDPLVVAATSCLTAFVLLCEAWEQRGAEDGGGALEGRGAQSCREALGATRAAVETARFALVETNDRARRVAAERAASRRAGGLRVPSVRTAAD
>NZ_CP023445.1|WP_096493994.1|3784927_3786940_+|carbamoyltransferase
MLVLGLNGNFSTAAEELVPGMLEFFFHDSSASLARDGELLAAVEEERYNRIKKTTRFPSAAVRACFEETGLGPDDVDAVAFYFPEDHVDKVLGQLYCQSPAVPLRYSRDLVRDRLRSELGWDLPAEKLHYVPHHLAHAMSSFGHSGFESALTVVFDGRGENASGTVYRIGPGGVESLASYPVHRSLGFWYLFGTQLLGYGFGDEYKVMGLAPYGDPARYRSVFESLHSLGEGGEYELLGNVVTPNAFLPAMLDTGFAPRRKGEEFTQDHKDFAAALQETVERIALHVIRHWAERTGERALCFGGGVAHNSSLNGVILRSGLFDRVFVHPASHDAGAGTGAALAVEHRLTGRVPRVALRRADLGGGLGDERDVVLKLKGWDGFVELVHRAADLEDLVDTSARLLADGAVLGWARGRSEFGPRALGSRSIVADPRPAANQTRINAMVKKRESYRPFAPVVTPDAAAEYFEIPDVEAELGFMSFVVPVRPEHRAGLGAVTHVDGTARVQVVTSTANPAFHRLVERFGELTGTPVLLNTSFNNHAEPIVQTFEDVLTSFLTTELDYLVVGDSVVRRRPDFLGALDDAVIRFRPETRLVGRVRFPVGGGRVEEHEVFLDYAEGPRKAISARAHGLLTRVDGKSAVAELVDGEVDDALRQEVLDLWTDRYFTLGPV
>NZ_CP023445.1|WP_096493992.1|3784364_3784712_-|hypothetical-protein
MKYMLLIHTSDERWQTLTQADKEEFLAEYAAFTEEIESTGEHCHGSPLTHRRNALSVRVRDGRAAVERGPLTDDDRYLAGYFVVDCADEDRALEIAARVPDAKLNVVEVRALAVV
>NZ_CP023445.1|WP_096493989.1|3783214_3784351_+|acyltransferase
MTPGPVLPPRLPSLTGIRAPLALLVFVAHALGSARFFADESVNSLGFLLPYGPAALSLFFVLSGFVLVWSEPWREGVGPYFRRRVVRILPTHVLTWAAVLLLLAALGPLPLLGPLPEVGPALVNLSLLQSLVPLPDYLLSVNGINWSVSCEVVFYLLLPLLSRPLLRVPDHRLWACFGVLAAVVLALPGVIGALVDGPPWALWPPLSFEQAWLVNFFPLTRLPEFLMGVVLARIVATGRWRPVRAWWPLLGVAAVWALLPVLPQVYARSAIAAVPLALLVPVIAVRDLEGRRSVLSRRWVRVAGDMSYATYLLHWPLLAVAKHVAGDRLLGLGEGLLLVAALYALTQGLSLLLHRWVERPLLRRAHRPRRSPAPDPAG
>NZ_CP023445.1|WP_096493987.1|3780351_3783189_+|AAA-family-ATPase
MAGGTVPTVQSGTVPAQRREATRSNHAPWRPVMRFQLLGPLEVVDRSRPVALGGTKQRAALGYLLLHPNSVVPTSSLLKALWPQDMPPTGRKMLQNAVAALRGVLTAAGDAPGAPALLTHTPGYLLRVDPEDVDLSRFRRLVHAGRADLAAGSWQRAARTLRDAIGLWRGPLLADLVEQGVDWPELAAVRNTRLAALEDCVEAEFASGRYGEMIYELERWVEAEPLRERLCGQLMRALYHCGRQADALGVYRRTRARLVDELGLDPGRELRELERAILNQEVPHRLPARREAAPAARSGATEGGGPVAAPPVAAPPAGIVPQRQAPPAPAPAPVALAPLPPASAPTAELKHVSVLMVLTRFEHDVAAAPPEEVDDALSDVATAVREEVERAGGVVTAKAASLIVALFGSTRSGEDDATRAVRAALAVRDRLAHGPRGAGPAALGVTAAVATGHALVRRHPGRAPEVGGGVLDRCMRLLAHVSPGEVRVCEETRGASEGAIGYDGPHDPVRGSWATGARQGAGGPPATPPLVDRDRELALLRGLLEQVGRRSRTHLVTVLGEPGIGKSRLVDEFQRVAETSATVVVRCPRLGGGGDLAPLADALAPRMGIGPADPVGLVAAKLAAAARGSGGAGERADRVLASLRVLFGLDVPDVLPDGSFAAWRHVLEDLGGADPLVLVLEDLHWAGEALLDFVDHLTAEATSSPLLVVVTARPELFDRRPAWGGGKAEASTITLDPLADQDVERLLTALCVRRGPATDEASAAYRAVIAHIGGNPLFAVEYARVLADAGPSSGGGGQSPPLPPLVRRVVAARIDSLPADAKAVLLDAAVLGEDLCEEGVRALGGGAVPDVARALEHLERREVLRRDRDAERATAYAFRSPLVRDVAYLTIPQHARAEKHRRAADWLERVPGHDALRLVHHGLRSGGCRPTEPSPVLPQPRQHAR
>NZ_CP023445.1|WP_096493985.1|3779607_3780270_+|SAM-dependent-methyltransferase
MGEQVVVTPALLDYLREVSQPEPAALAELRAETALLPGGGVLPVPPGEGAFLAMLVALTGARLVVEVGTFTGCSTLCLASALPDGGRVITCELSPKWPAIARPHWERAGVADRIEVLVGDAAGSLAGLTGELAGRVDLVFVDADKAGYPRYYELAVELVRPGGLVVVDNTLFSGRVADPAAVDPDTEGVRELNRRIAADDRVQAVLLAHADGMTLARRTR
>NZ_CP023445.1|WP_096493983.1|3778217_3779615_+|HAD-IIIC-family-phosphatase
MSGDLVKCLVWDLDDTLWRGTLAEGDAPVLDERVRAAIVELDARGVLQSVASRNDPEPALAALEALGVAEYFVLPEIGWGVKSAAVARIADRLGFAHRAIAFVDDRPAERAEVAFHLPEVRCYPAERVLELCSLPEFSPAVVTEDARNRRALYRAGFARGAEQAAFTGPDEEFLRSLGLVLRIDRARPEDLHRVEELTARTSQMNATGVHYPHGQLRALLDDPAHEVLVAGLTDRFGPHGAIGIVLLERHTAAWHLKLLATSCRVVPYGVGSVLLDWLCGQALEAGAHLVADFRRTDRNRMMEIAYRFAGYDDADCACRAELAAVGGGPEHLAAAGAPGAGAPGIGASGAGASGAGAPAGGAPAGGAPGTGAAETRAAEPRAAESRVAEPRAAESRVAEPRAAESRVAEPRTAEPRAADVPVAEVPEARASGNPVRRLHLRPAPRPAPRAVTVEAPSLLEVPTRG
>NZ_CP023445.1|WP_096493981.1|3777105_3778221_+|acyl-CoA-dehydrogenase-family-protein
MADRVDEATALVERVVADRAGEWDLAGELPVAALRELGAAGALCGEVAERHGGLGLGSLDNGELTARTGALCGSVRSVQTSQGMAAWTVRRLGDQAQRAAVLPRLTGGSLAAVALSEPGAGSDLSAMATTVEDDPGEPGTVLVRGHKVWTTAARYADLLLVAGRRGDGAAVALVPATAPGVTITPVANPMGCRAAGHADVELDDVRLPATSVLGGDGVSTALLVTTVLAHGRLSVAWGCVGILRACLAASAEHARTRRQFGVPLAAHQLVAGHLADLLVAEQVSTRVCEHASRRWDESSAELVTATVLAKHVSAGHAARAAATAVQVLASAGAHDGHPVARAYRDAKLMEIIEGSNELCRLVLAEHAVATA
>NZ_CP023445.1|WP_096493979.1|3776840_3777113_+|acyl-carrier-protein
MTSGTESRTDDVQGAVLDFLRARTGAEWDAERDLFAEGGLSSLFAMELVVHLEQCFDVEIAGPDLRLDNFRTVRAMTALVDRLRAGGAGG
>NZ_CP023445.1|WP_096494002.1|3789396_3790563_+|DegT/DnrJ/EryC1/StrS-family-aminotransferase
MHLKAPQKLEFPAWPQFDSTEREALLRTLDSGRWWRITGDEVVSFEREFAQAHGARHALAVTTGTHALELVLEVMGAGPGTEVIVPAFTFISSSQAAQRLGAVVVPVDVDPDTYCVDPAAVRAAITERTRAIMPVHMAGQLADMDALRALSAETGVPLLQDAAHAHGARWRGEPLGALGSIAAFSFQNGKLMTAGEGGAVLLPDGDQHEEAFLRHACGRPLADRAYHHRTAGSNFRMNEFSAALLRAQLGRLQQQTDVRERHWPVLSRLLAEVPGVVPQGTDPRCDRNPHYMAMFQVPGIGEERRARLVDALVERGVPAFAGFRAIYRTAAFWERAAPDTTVDALARACPVTEALSSDCVWLHHRVLLGAEEQMPLVAEAVACALEEA
>NZ_CP023445.1|WP_096494004.1|3790893_3804948_+|type-I-polyketide-synthase
MLRSDLIRPLPELLREHAAERGDRVAFRDARRAVTWVDLELRTRRLAGHLAARRLLPGDRAVILLGNRVETVECYLALVRAGAVGVPLNPVSTDAELGALLDDSGARLVLTDAAHADQLAGLRATRPALEVVHVDRDYEALAGVDAPLPAHDALELDDLAWMLYTSGTTGAPKGVLSTQRNCLWSVAACYAPVLGLTPDDRVLWPLPLFHSLSHIAGVLATTAVGATTRVVDGRSPQDVLAALHEERSTVLAGVPTTYHHLVRAAGERGFLAPDLRVGLVGGAITTAELRAAVEQRFGVPLIDAYGSTETCGSITVNWPTGPRVEGSSGLPVPGLAVRLVDPDTGLDAPTGAEGEVWVRGPSVMVGYHNRPEATAAALRDGWYRTGDLATRDESGFHAVTGRIDDVVVRGGEKVHPAEVEAVLRAVPGVADAAVVGRPHDVLGEVPVAFLVPGEGFDPAQVLAVCRERLSYHKVPEELYQIESVPRTASGKITRRVLLDTPARLRASGERGALFRTDWVPLAAAPGGATAPGAVAGSGAATASSAVTGAGAATGPARATTPAAATAPATTPAEASTPVAAARPGGHPVAVMAEPTAPAPGGAPVVLDLRGDDAPALSGRPDLVLTRGAVAVDGGPVRLGQLAAWTAACRAGITAVDADDDGAVDPVGLLAAGEPRLLVRSGVVLVPRLHEVPGSVVGRGALDPRRAVAVTGADSGTAAALARHLRGAHGVRDLLLITAPHGRARAGALRDDLVASGARVVLAVAGPDALDRALSRAPSPLGALVHTGDGDPEALPRLLGARVELVVCATAFDSAAAEDVVLRRRAAGMPARCLAWGPWEAETAQARPGLAVLPLRDGLAAFDAALGADEPVVSVLRPDPDLVAGDVPAPLRDLLHVVAAEPEPVRVAELRASLAGRGERERRRRLLDLVRAETAALRPAEFLVDGHERGFAELGFTSATSVALRNRLTAATGLALPATAAFEHPTPTALAALLHDELFGASRTPVAPARAVERPVERSGEPIAVVAAGCRLPGGVASPEDLWEVVRSGADVVSPFPVDRGWDLDALRGACAGGGFLADAALFDAALFGVHPREALAMDPQQRLLLEVAWEVFERAGIDPRSVAGDGTGVFAGLMGHDYGSRPGLDRQLVEGYLSTGNAGSVASGRIAYAFGLTGPALTVDTACSSSLVAVHLAVQSLRRGECSMALAGGATVMATPADFVEFARQGALAPDGRCKPFSASADGTAWSEGAGLVLLERLSDARRNGRRVLAVIRGSAVNSDGASNGLTAPSGAAQQRVIRAALADAGLSTSDVDAVEAHGTGTRLGDPIEARALVATYGRDRDGEPLWLGSLKSNFGHPQGAAGIAGLIKLVQALRHGVLPRTLHVDAPTPEVDWDGVEVLAEQRAWPEVDRPRRAAVSSFGVSGTNAHVVLEQAPAETAAPAAPERGPVPLPVSAVDAAALRAQARRLADFLAPSDVTAAELAGALRAGRADLGERAVVVAADRAGALAALEALAADEPSPALVTGRADVTGRTVLVFPGQGGQWVGMGARLLDESPVFAERVGECAAAVDPLVDFRVVDVLRGGDLSRVDVVQPVAFVVMVALARLWRSVGVEPDAVVGHSQGEIAAACVAGALSLADAARVVVLRSRAIAAGLNGGGMASIPLPQAQVEELVAGTGVCVAAVNGPGSVVVSGEVDALVARVEGARRLPVDYASHSPAVDVLREGLLADLAPITPRPAAIPMLSTVTGKWLDGAELDADYWFANLRHPVRFADATALLVADGFRAFVEVGAHPVLTAPVQDLLAGAGPSVATGTLRRDDGGLDRFLRSAAELHVRGVPVDLSPLAPPPVRALDLPTYPFQRARYWLDADPTAASALRHPLLTSATDLAGGEDLVCQARLSTARHPWLADHAVRGSAVLPGTCWAELAIRAGDEVGAPALDELLVEAPLVLPERGAVEVQLRIGAPDAAGRRPLEAHARAEGGAWTRHASGSLAADRSTPVPLTEWPPTGAREVDLAGFYDSRAAEGYDYGPALRGLRRAWTRDGEVFAEVELPAPLSPDGWGLHPALFDAALHATGLLPPARVAADEVLLPFSWRGTRLRATGATALRVRLTGTADDHVLRAYDPEGAPVVEVDALRLRPAPATALVGSGALFRVEWVDLDLPVSTPDSTPGAPVLDRPVLDLPGGDARTLVGLTLEALREHDELTVVTRGAAEDPAAAAVWGLLRTAQTERPGRFAVVDLDDDPASRALLPALPATGEPQVRVRAGRASAPRLARTRDDGLPLPAAPTWRLTCDGGTFTDLAATPSPAANRPLEPGEVRVGVRAAGVNFRDAAVVLNAVPGQRGLGGEAAGVVLETGPGVTGLAVGDRVLGTFDRDFGAFGPVAVTDARLLAPVPPGWGFARAASVPVAFLTALYGLRDLAQVGPGDRVLVHAGAGGVGGAAVRLAALLGAEVFATASPAKWPVLRALGLDDAHLASSRDTGFAERFPNVDVVLNSLTGELVDASLRLLAPGGRFLELGKVDVRDLVRADVTYRAYDLRDAGPDRTAELLAEVLGLFAAGRLEPLPLTVRDVRHAPEALRHVASGGHVGKVVLTVPRPLDPEGTVLVHGGGALGALTARHLVSAHGARHLLITSRRGPDAPGAAELAADLAELGATTRFERCDAADRDRVAALLADLGGRPLTAVVHTAGALDDALLADQDAARVDAVLRPKLDGALLLDELTRDADLAAFVLFSSAAGTLGNAGQANYAAANAALDALAARRRSAGLPATSIAWGHWEHTSALTAGLTAADLARGARHGAGSLTTTEALALLDAALASPEPAVLAAALDPRRAAEVPPLLRDLAGPRRAVAAQAVAGADRPLIDVVRAHTATVLGHRDASAVDANRAFKELGVDSLTAVELRNRLAAATGLALAATSVFDHPTPALLTAHLLAELGHAPAAGTTAPPATAAVTADAGEPIAIVSMACRFPGDVSSPEDLWDLVAGGGDALTPFPADRGWDLAALFAPDPDRAGRSHAREGGFLADVAGFDADLFGISPREAIGTDPQQRLLLEVAWELFERAGIAPDSLRGTDTGVFAGVIAHGYPVLPAHSDQGLEGHRVTGVSGSVVSGRVAYAFGLQGPAMTVDTACSSSLVGVHLAVRALRGGECSLALAGGVTVLSTPDLFVDFSRQRGLAADGRCKAFGAGADGTGFGEGVGLVLLERLWDARRNGRRVLGLVRGSAVNSDGASNGLTAPSGPAQERVIGRALADAGLSAADVDLVEAHGTGTRLGDPIEARALVATYGRDRGGEPVWLGSVKSNIGHTQAAAGVAGLIKAVQALRHGVLPATLHAAEPTPEVEWDGVAVLAEQRDWPEVGRPRRAAVSSFGVSGTNAHVVLEQAPEELSPEGRIPEVRIPDRRTSEGRVPEGRAPEGRTSGGRAPEGQTSEGRAFGGRVPEDQTSEDRTSEGQASMGRAPEGQAPLGQVSESRAPDHRVPAGPDRDVPGHLPLVLSAHDPAALRATAARLLPVAERVPLPDLALSLVTGRAALPCRAVIPARDRGQALAALRDLASGATAPAERDGGGVAFLLSGQGSQRAGTGRLLERRFPVFRDALREVCALLDRRVVGGPGVRAALDDPGLLADTRYAQAGLFAVQVALVRLLDALGVRPDLLAGHSVGEIAVAHAAGVLSLEDASTLVAARGALMRELPPGVMVAVRAGEDEARAALVDGVELAAVNGPRATVLTGDEAAVTEVAARLGRATRLRVAHAFHSAAVDAVLPAFADVLARLDFRPPRVPVATTAPGALDAPEYWLGQAREPVRFADAVTDLHRRGATAFVEVGPGGGLAAAAQECLDGHDVLCAPLLHRDRDEDHSLITALGALHARGARVDFAPLLADAGGRTTDLPTYPFQRRRFWLDPAPPTTDAAPLEHPLLTGELEIPGSDTAAFTGRAATGAHPWLADHRLLDAVVVPGTALLDLVRAAGRQLGLPEVAELVNEVPLVLGDGAALLRVTAAAPGPDGRREVAVHSRPESAGPRSPWTRHVTGQLAPESGPLAFDLAQWPPPGALPLPVADHRAAMAATGHGYGPAFLGLRAAWKLDDEVLVEAVLPDEVADDGHAVHPALLDAVLQAIALTGVEDGSQVRVPFSWRSARGAGRAGRAVRASLRPDGDGGVRVRVACPRGRPLLEIASLVSRPVTPDRLRPGVLLRQAWTEVGPPPGAAEPVPLREVGERVPPVVRVDAGHVRDLLPLLQEVVTEPRWESTRLLVTTSGAVGPRAGRAEGAAVWGLVRSAAAEHPGRFVLADLDDRPESAALLPALATGALPEAVLRAGRVLVPGLHRVSAPGAGGAVLDPGGAALITGGSGALAALLAEHLVRAHGVRCLVLLSRSGRGPDVPGADVRHVRGDVANRADVVAALAAVPPDRPLTLVAHLAGVLDDGALTALTPERLDAVLRPKAEGARHLDELTRDRDLAAFVLFSSVAGALGHAGQANYAAANAHLDGLAHERHALGLPATALAWGPWTEGMARGRGTLSPQVALGLFDAALRTGLPALVPLDREPERRVPAPRAATPAPAGPSLADRLRPMPPAERRAHLLELVTAEALGVLGHDDGAALPAGQAFRDAGFDSITAMALRNRLVRLAGVRLPASVVFDHPTPAATAERLEAELFPADRLPGPRHGDDFDDMAADELVRRALGGE
>NZ_CP023445.1|WP_096494006.1|3814271_3815480_+|glycosyltransferase-family-1-protein
MRVLFTVTGAPSHAHEMLVLGRAVLDAGHEVLVATAPSAAPGLRGSGLPSVEALPDQARFWVERLGGVAPPARPGTDYPGVAAIVDVIAGRPLLREALTGLRPVVDRFRPDLVLRDGMELAGLLVAEERGLPCLTVPSGTTNQLDPAAVLPRLNERRAEQGLPTSADPLGAHRHGHVDCLPREYSLLGVPLSPCLAYRPPSPDGRSLPAWVADLDPSRPLVYGAVGIALAALWRRDDVTALVADPVEALGGLVAALSEVDCAAVVSTGGIPVDRVPPGAPHVRVVERAPQPLLLECAQLFVTHAGANSVREAVRAGVPMVAAPLFGDQPHNAARVAALGLGVRVVDGSPADLADACRTVLADPRFTARARHARRTLLALPPVGEVVTRLEQIADAARSVAVV
>NZ_CP023445.1|WP_096494008.1|3815575_3815818_-|acyl-carrier-protein
MATGETGFDDVSFDLISVQYHSLKAGHDYGQYVRDADNAGRQDIADFFRRVMDEDAARAKECHRFLAELTGSSESGPAMS
>NZ_CP023445.1|WP_096494010.1|3815997_3817023_+|SDR-family-NAD(P)-dependent-oxidoreductase
MPRRLAEQVVVVVGASSGIGRVTALRFAAAGARVVCAARNTRALDGLVEEVRGAGGRAVAVTADIADEAAVRAVADVAVERFGRVDTWVNAAGIGVYGRVEDTPAGEFDRVMRVNYLGHVHGAKAALPALRRAGGGVLIGVASVLGLRSAPLQAPYAASKAAVRAFYDALRVELAHDGESIAVTAVLPAAINSPFFEHCRSRVGSLPKPPPPVYAPELVAEAVLRAAERPRREVPVGDAALAFYLGQRLFPALTDALMSVRAVGRSGMRSELPDNGVDNVDSPVDEDGRVHGSYPGRVLDSSPVTALLARVPRPGELATSLVSGAHRVGGAVRGGLRAARS
>NZ_CP023445.1|WP_096494012.1|3817077_3817542_-|DUF4383-domain-containing-protein
MTDTTTRHRTPVQNAALAVGAVFLLVGIAGFVPGLTTNYDGLEFAGHHSDAALLGVFKVSALHNLVHLAFGAAGIAAGLSKAPRGARAFLIGGGAIYAVLWLYGVVVDEHSTANFVPLNAADNWLHLGLAVGMIGLGAALGRNAAHYRAARSDD
>NZ_CP023445.1|WP_096494015.1|3818416_3821434_+|cytochrome-P450
MVATGTRIPGPKPLPLVGNLLDVLTSDLDTDVDFLDRCHREHGGIVALTFAGQRQVFASSHELVARMCSDPSWGKAVHPALEQVRDFAGDGLFTARGDEPNWGKAHRLLMPAFGPTAMRDHFPAMLDIAEQMLVRWRRFGPDHRIDVADDMTRLTLDTIALCAFGARFNSFYRDRAHPFVDAMVRSLVEAGERAERLPGVQPFLVGRNQRYRDDIATMNRIADGIVAARAALPAGERPDDLLERMLTCADPVTGERLSARNVRYQLATFLIAGHETTSGLLSFAVHRLLAHPEVLRKAKDAVDGVLGDRVPAFEDLARLDYLGQVLRETLRLHPTAPAFALAPDEPAELGGHAIGAGEPVLVMLPTLHRDPAVWRDPDVFDPERFAPERMDEIPACAWMPFGHGARACIGRPFALQEATLVLALVLQRFDLALADPDHRLTIKQTLTLKPDSLVVRARPRADRPGATATVETVVPHQVPATHRHGTPLHVFYGSNGGSGEGLARTIAGDGAARGWATSVAPLDDAVRALPASGPVVIVSSSYNGAPPDNAAHFVRWLTQDGPDLSGVDYLVLGCGNLDWSATYQRVPTLIDEAMAAAGARRLRERGATDARADFFGDWERWYEPLWPLLSAECGVEVGEIGPRFRVVESDAADGLGDLASAVVLENRELVRGPDAGSKRHLELRLPDGTSYRTGDYLSVLPQNHPDLVRRAVARLGTRAERVVTVESSAPTGLVPVGRALRVDELLTRCVDLSAPAGAGVVARLAERCPCPPERAELAATTGATLLELLERFPSCAVDLALALELLPAPRTRLYSISSAAEEQRAEVALTVSVTGVTSGYLSRVRPGDRVAVGIASPPESFRPPADNTVPVVLIAAGTGIAPFRGFLRARAALGGEPGPALLLFGCRGPELDDLYAEEFAALGDWLEVDRAYSRHPDGEVRHVQHRLWQRRDRVRELVDAGARVYLCGDATRVGPAVEEVLGRIGPGAGWLDALRAGGRYATDVF
>NZ_CP023445.1|WP_096494017.1|3821473_3822520_-|RNA-polymerase-sigma-factor
MWIGYSADGRRRRPVRWWGVTEAFTWETDEDIKLAATLRRDAEAANAADSTRAYLKAIGRVRLLTADQEVELARRVEAGLYAEHLLDLPPAARGSRRPVELRRVVRDGQRAKDHLLEANLRLVVSIAKRYTGKGMALLDVIQEGNLGLVRAVEKFDYAKGFKFSTYATWWIRQAITRALADQSRTIRLPVHMVEVVTKLARIERDLLHRNGREATAEEVAVELDVTPEKVVELRQHARTPVSLDQTIGAEADTSIGDLIADENAVAPLEAVSSALLSADLRAVLETLTPREAGVVRMRYGFPDGVLHTLDEVGRVYGVTRERIRQIESRTMAKLQHPARSRGLEGYLD
>NZ_CP023445.1|WP_157767680.1|3822879_3823227_+|hypothetical-protein
MDHRAERQDSGEAVVGQVERAQVRGEVAEAAAEVRHAGAGAQELGERGQQGAFEGEGPEDVAEQVRVAVGDGVVRGPGGAAEAKAAVLLASTTAALPAGALHARRGRWPARQAGR
>NZ_CP023445.1|WP_096494018.1|3823211_3823784_-|deaminase
MRKLVYFIAASIDGVIAGPEGEHDFYPTAEPMVEHLRAEYPETTPTHVRPLVGMPLDTPNRRYDTVLMGRGSYQPALDAGVGSPYAHLRQYVVSRSLPDADPAVALVRADPVGLVRELKREDGLDVWLCGGADLAGQLLPEIDELVVKTYPVVAGGGTPLFRAGFAPRAFRPVDVRAFDHGGVVTTYRPA

Crispr_ID: NZ_CP023445_8

• CRISPR_ID: NZ_CP023445_8
• CRISPR_location: 5326850-5327067
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP023445_8

Consensus_repeat	Method
GCGGGTGGTGCCGCCGAGCGGGTCGGTC	CRISPRCasFinder

spacers of NZ_CP023445_8

>8.1|5326878|35|NZ_CP023445|CRISPRCasFinder
TCGGCGACGACGCGGCCGAAGGCGTCGCGCTCGAA
>8.2|5326941|35|NZ_CP023445|CRISPRCasFinder
AGCTCGGTGATCAGGCCCGCGGCGTCGGTGCGGTA
>8.3|5327004|35|NZ_CP023445|CRISPRCasFinder
GTGGCGGCGAGGTGGCCGCGCTCGTCGTAGGCGAA

CRISPR arrays and Neighbor proteins around NZ_CP023445_8

CRISPR arrays

The CRISPR arrays of NZ_CP023445_8

>merge|NZ_CP023445|8|5326850-5327067|CRISPRCasFinder
GCGGGTGGTGCCGCCGAGCGGGTCGGTCTCGGCGACGACGCGGCCGAAGGCGTCGCGCTCGAAGCGGGTGGTGGCGCCGAGCGGGTCGGTCAGCTCGGTGATCAGGCCCGCGGCGTCGGTGCGGTAGCGGGTGACCGCGCCGAGCGGGTCGGTGGTGGCGGCGAGGTGGCCGCGCTCGTCGTAGGCGAAGCGGGTGGTGGCGCCGGTGGGGTCGGTCT

>NZ_CP023445|8|7|5326850-5327067|CRISPRCasFinder
GCGGGTGGTGCCGCCGAGCGGGTCGGTC	TCGGCGACGACGCGGCCGAAGGCGTCGCGCTCGAA
GCGGGTGGTGGCGCCGAGCGGGTCGGTC	AGCTCGGTGATCAGGCCCGCGGCGTCGGTGCGGTA
GCGGGTGACCGCGCCGAGCGGGTCGGTG	GTGGCGGCGAGGTGGCCGCGCTCGTCGTAGGCGAA
GCGGGTGGTGGCGCCGGTGGGGTCGGTCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl|CDD|270703
NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein	unknown	unknown	gnl|CDD|377856
NZ_CP023445.1|WP_096495563.1|5333519_5334146_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495554.1|5319150_5320410_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495559.1|5324343_5324823_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK	unknown	unknown	gnl|CDD|224588
NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein	unknown	unknown	gnl|CDD|340861
NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_CP023445.1|WP_096495564.1|5334142_5334463_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497934.1|5337516_5338836_-|transcriptional-regulator	unknown	unknown	unknown
NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376791
NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein	unknown	unknown	gnl|CDD|223314
NZ_CP023445.1|WP_157767790.1|5323622_5323997_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495568.1|5335636_5337184_+|transcriptional-regulator	unknown	unknown	unknown
NZ_CP023445.1|WP_096495558.1|5324003_5324357_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein	unknown	unknown	gnl|CDD|380454
NZ_CP023445.1|WP_096495569.1|5337168_5337528_+|signal-peptidase-I	unknown	unknown	unknown
NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein	unknown	unknown	gnl|CDD|223609

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein	gnl|CDD|270703	cd05154, ACAD10_11_N-like, N-terminal domain of Acyl-CoA dehydrogenase (ACAD) 10 and 11, and similar proteins. This subfamily is composed of the N-terminal domains of vertebrate ACAD10 and ACAD11, and similar uncharacterized bacterial and eukaryotic proteins. ACADs are a family of flavoproteins that are involved in the beta-oxidation of fatty acyl-CoA derivatives. ACAD deficiency can cause metabolic disorders including muscle fatigue, hypoglycemia, and hepatic lipidosis. There are at least 11 distinct ACADs, some of which show distinct substrate specificities to either straight-chain or branched-chain fatty acids. ACAD10 is widely expressed in human tissues and highly expressed in liver, kidney, pancreas, and spleen. ACAD10 and ACAD11 are both significantly expressed in human brain tissues. They contain a long N-terminal domain with similarity to phosphotransferases with a Protein Kinase fold, which is absent in other ACADs. They may exhibit multiple functions in acyl-CoA oxidation pathways. ACAD11 utilizes substrates with carbon chain lengths of 20 to 26, with optimal activity towards C22CoA. ACAD10 may be associated with an increased risk in type II diabetes. The ACAD10/11-like subfamily is part of a larger superfamily that includes the catalytic domains of other kinases, such as the typical serine/threonine/tyrosine protein kinases (PKs), RIO kinases, actin-fragmin kinase (AFK), and phosphoinositide 3-kinase (PI3K).	7.07188e-19
NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein	gnl|CDD|377856	pfam07508, Recombinase, Recombinase. This domain is usually found associated with pfam00239 in putative integrases/recombinases of mobile genetic elements of diverse bacteria and phages.	6.13554e-15
NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator	gnl|CDD|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	6.96793e-08
NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein	gnl|CDD|223609	COG0535, COG0535, Predicted Fe-S oxidoreductases [General function prediction only].	5.35451e-24
NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	0.000284351
NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein	gnl|CDD|380454	cd19531, LCL_NRPS-like, LCL-type Condensation (C) domain of non-ribosomal peptide synthetases(NRPSs) and similar domains including the C-domain of SgcC5, a free-standing NRPS with both ester- and amide- bond forming activity. LCL-type Condensation (C) domains catalyze peptide bond formation between two L-amino acids, ((L)C(L)). C-domains of NRPSs catalyze peptide bond formation within (usually) large multi-modular enzymatic complexes. NRPS can use a large variety of acyl monomers (approximately 500 different possible monomer substrates as opposed to the 20 standard amino acids in ribosomal protein synthesis) to construct bioactive secondary metabolites of 2 to 18 units long (with various activities such as antibiotic, antifungal, antitumor and immunosuppression). In addition to the LCL-type, there are various subtypes of C-domains such as the DCL-type which links an L-amino acid to the D-amino acid at the end of a growing peptide, starter C-domains which acylate the first amino acid with a beta-hydroxy carboxylic acid, and heterocyclization (Cyc) domains which catalyze both peptide bond formation and cyclization of Cys, Ser, or Thr residues. Typically, an NRPS module consists of an adenylation domain, a peptidyl carrier protein (PCP) domain (also known as thiolation (T) domain) and a C-domain. NRPS modules may also include specialized domains such as the terminal-module thioesterase (Te) domain that releases the product via hydrolysis or macrocyclization and any of various C-domain family members such as the epimerization (E) domain, the ester-bond forming C-domain, dual E/C (epimerization and condensation) domains, and the X-domain. Streptomyces globisporus SgcC5 is a free-standing NRPS condensation enzyme (rather than a modular NRPS), which catalyzes the condensation between the SgcC2-tethered (S)-3-chloro-5-hydroxy-beta-tyrosine and (R)-1phenyl-1,2-ethanediol, forming an ester bond, during the synthesis of the chromoprotein enediyne antitumor antibiotic C-1027. It has some acceptor substrate promiscuity as it has been shown to also catalyze the formation of an amide bond between SgcC2-tethered (S)-3-chloro-5-hydroxy-beta-tyrosine and a mimic of the enediyne core acceptor substrate having an amine at its C-2 position. C-domains typically have a conserved HHxxxD motif at the active site; mutations in this motif can abolish or diminish condensation activity. An HHxx[SAG]DGxSx(6)[ED] motif is characteristic of LCL-type C-domains.	5.9327e-40
NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK	gnl|CDD|224588	COG1674, FtsK, DNA segregation ATPase FtsK/SpoIIIE and related proteins [Cell division and chromosome partitioning].	6.62921e-13
NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.33471e-41
NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein	gnl|CDD|340861	cd17507, GT28_Beta-DGS-like, beta-diglucosyldiacylglycerol synthase and similar proteins. beta-diglucosyldiacylglycerol synthase (processive diacylglycerol beta-glucosyltransferase EC 2.4.1.315) is involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. This family of glycosyltransferases also contains plant major galactolipid synthase (chloroplastic monogalactosyldiacylglycerol synthase 1 EC 2.4.1.46). 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. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common 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.	1.84673e-06
NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000177543
NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein	gnl|CDD|223314	COG0236, AcpP, Acyl carrier protein [Lipid metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	4.29477e-06

Protein sequences

>NZ_CP023445.1|WP_096495559.1|5324343_5324823_-|hypothetical-protein
MTPAWADRLLPADAALLARCFPGGRAGLSGSLLRSVRLDRVGPACSLRLDLPGDGPGATQAHLGMLAVADVELAGGALPQRVDVEITDLPGRRVAVVVAGGGLRLSLTCAEVLRFGRVSDHDTPPGAVDDGPHRFVGRLDQRLHRVVPGPEDENYHARF
>NZ_CP023445.1|WP_096495558.1|5324003_5324357_-|hypothetical-protein
MPASDDFPGDFPGDLDALHWDERGDAVTATFEAGLDDAGRAAWGAEAGHTRVRYHVRFAGVADLRVAGFDHRLPLRLAVIADGARVGVEVSGAGTDVRFTSAPPEHVGHRTFTAAAP
>NZ_CP023445.1|WP_157767790.1|5323622_5323997_+|hypothetical-protein
MLRTTSRAAMTGFAILALAGAGAGSATAVERELTTIAVPPLQPAGGEVKASSVACVWKYSPGRNPTVWVDCHQVGGGAATGFEVTVTCSDGSSHTSGATRFGSPAMAYCPGATTMKSFTLSAHY
>NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein
MPRTWPASPFQHTIMTNDGTIPSGSTGPHMTMSISALVTGGLDVDLLDAAYDDLVARNDVLRTTLEPDGEQWRQRVHPHRTAHLHRAEAAAPEAQSFVDAWSREPVPIDRPPLVRGQVVALDDGSHLVNLVFHHVHTDPPSLVLAVAELGALYTARLAGEPLPPPPLQYGPYSARRAAITAPTLDADLDHWRTTVEGARPLDLSPSRDLSTPPDSGVLRLDVLDGRDAAALEKWALRRRTTVFATLFTAFCLAAADRSTTRDVLVNTVFEQRAHPDVRTLIGPFLHPSVLRVRVPEGATWSSMTPVVREAVGAAYARAHVPGFDVLRLHPDVIHAVETEPVGLCVFQYLPYSGLEDTFAYGPATARVLARTQAGPTGDVGLMFRLHRRSSGSLYATVTYDRRDLTEPVVRALFTDFTTRLREPLAERAPRTGSPSRPRDTAAPQRDSAPVT
>NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein
MHPRTARTLNQKEFHDLRRTVAIRAETRRNIEVDATYATPLPREVSLQLTYKCNLRCNHCYQWNDQGFFHDFSKVKQRTELDLDIVDDVLRMTDDTRAKVFLWGGEPLMHSRFGEVAELLARTPRTVNLCTNALLVKRNLEHLLTIGPGLNVLVSLDGLGADHEALRGKGTFPRTIDNVRLLLDLQKSGEYQGEVSLSCMVSNETVGSMREFMEWAEELGVNSVYFQFPWFISPEVASAMDDMYAENFAWLNPPAPGTTPTWHSYTYRIEPGLIDTLWRSMAELAERTWNVRIRYQPQLEPDEVEDFVLGTSRPAQKRNRCLAVSNRLEVHADGKVSSCKFFPEFVIGDLHESGVAEVWQGEAFRRVRSVLRGTSLMPVCSKCILLYLNGV
>NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein
MRIKEVLAGVLGAPELVERITDATNVVQDLGINSIQMINFLLALEDAFDVELEFEELSFEQLESLPEIRRFVVAAMPDSP
>NZ_CP023445.1|WP_096495554.1|5319150_5320410_-|hypothetical-protein
MTGARALRLGAFDVERRWRPDGLAALPEIVDRGADVVASAMDELLAVACGPGDVLVTGAPVPVAWHEVLAGAGIGFEHRVAPGGVGGSVEQRLVARPPADLGGLGFEPYAVLPESAGVVGALGLRAELPDWRVVRAVSSKSWSNALVRELGLAGAGVVVDSVAGLQAQVEALDGAPALLKDPFGVSGRGTLALTSPLVLRSVVRVLDKQVRRGLDVEVLVQRRFDPVADFSAQFSVRPGGRVDWLGTRLIENTGFAYAGSRPAPPWLAERLSALGYREIMADVGAALAGAGYRGPVCVDSMLLRDGTLVPVLEINPRTSMGLISVLAGRRLAADPERARLVVRPVRGGAGFDRLVALLRADGVLLEAGGGGVLPLSSGTLASSRGRLYCAVVARDEAGHRALGAALDAVLGAWQVDRAS
>NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase
MPRELGLIGATAIAVRAVLDPARRREDVRVRAIAASTPERAEAFRAEHGLPVAHADYRSLVRDEGIDTVYVSLHNSAHARWAAEAARAGKHVVVEKPLCLGRREAHALRRAAGDAGVHVVEAVITTGHPWQAAVRELVASRELGELTGISSHIAFDLPPGAGYRFRPELGGGAFHDTASYWLDAVQAVVGLGGATASGHSEFSGPNGVDLEFDAALRLPSGVRAELRASLVGPYRADHEFRFTGGKARLRNFLRPAAGPFPVNLVLQRDGGAREVRSFPAVSYYDAQFDRIMALLARPARPDDAVVERITVLESAYLNALERCARTGRAEA
>NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein
MAVLTSGVALGVHVPGLLLARRLAEVGVAARVDVLENHLPERLRELIPASKTAFHRDFRVALAGQRLAARNTTEPDEGLVAGLWREWERDGVELLVVLSGFWLPTAHRYASAHSGVRVRSCHVDSVASPSFTSASGAGRGRWGEHEDVWLLERAGSAVARTIPVSREEPEPWGDRDGRLLAHGGGWGMGTYRTGAAELGAAGFALDVVAYERSEVPEEQGRNRYFMIDPDWHPWHDTGFPPFGRVHDGAVEYRRRAEHHDGFDLTRRAIAVVSKPGGGTLMDSLSAATPVVLLEPFGAHEARNAELWRDLGFGIGYREWVDGGRQVAVLEALHRNLVAARGRVLSYPDELAGR
>NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein
MRSTTKRSLSDEELRAAVTEAFGPRATITSSRELADGTFNAVWLLDVDPVGPVVLKAAPPDDLPLLTYERRIARTEAAVLRAAAATAPVPVLHHAGEGSAGVGGDFLITSVVEGDTWQRVSGELGGAERARLRRELGRAVAGLHAVRGTAFGYPERSTGLHGGTWYEAFTAMVDGLLADARRFGVTPPGRPTALHDLAVAGRALLEEVTEPVLVHFDLWNGNVMLTGEEGERRLSGLIDLERAFWGDPCADFVSLALLGELSDDDPLLDGYREAGGPAQLTATTRRRIALYQAYLYLIMIVEAVPRGHKGVKSAAAQALFRSRYRRALRRAAP
>NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein
MTVEISRDPWETLDRLLGVEVAEAVGDGIGAVAFYGRCSTEDNQDPETSHGWQLGNARKFVEPLGGHVVVEFFDVGQSRSVPWERRPEAARLLAQLKNPQRGWSALVVGEGTRCWFGNQFSLIAPRFAAYGVELWVPELGGRFEPRNPSHKMLMSVLGGMSESERQHVQARVRAAMDSQVVNEGRHQGGRAPYGYVVVDGGPHPNPRKAAEGYRLRKLAVEEASAEVVRRIFAEYLSGRGDRAIATGLNRDAVPCPSARRPDQNPHRLADGWQGSTVRAILDNPRYTGFAFFGRWTRQEMLLDPDDVAAGHVVRFRRATADKVVRSRKPAHPAIVGVEEFTQVQLLRKSKSAGGLKTARKAERSERPTKRPYLFRGRVRCTICGRKMEASPRARGVYYRCPARTLAPGAPALAEHPPTVYLREDVLQDAVNGWLGGLFAPQNLDRTVAALVASQEGAAGKGDSREAARLRLSKAEEQLSRFQEAIKAGIDPLALVEAVNEAQAVRTAAKAELEGLPVPNLLGAAEVHAMIDSLGNVGAALKGAGIERVAGLYTAVDLQVRYTHTARRADVIIKPAGCVNNVRVRGGT
>NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK
MNGDLVHVEPVLVGEVVAEPAALVRLVPVAWRSRQAWRDVAIRLLRLPLRFFPAVGRGALVVFRAWRRWVRVRDYREAAEQAEKLADKYVEIRELGLYRWRVTGMVLGLVSALLFAGHVVWGGVLLWGVAGGGAAVVAVIGRRKDGSPGRKAVLDGSRVLAWTMDAQLLVDAFRDAKLIGKDETLRLVERPHRVGDGWAVVADLPATRKAVDVIKNRDALASALAVDEVQLVAERVRGRGGHAGRVSLWVADEDPYAGAPLRAPLLDVERWDAWRAVPFGRDARGRRVDLPLVWTSLLVGAIPRQGKTFATRLAVSGFVLDPYARLYVFDGKGGKDWEAAEQIAYRYVCGDEQEHAEAVRDHLVALVAEVQERYARMATVDDELCPESKITPALSRDPDLGMPVTGVVIDEVQVYLENTARVEVGGRKTTLGLYVADLLTYLVRKGPAAGIVVVLATQRPDSNTIPSRLRAVLGSRFALRVMDWRDSNIVLGEQMNTRGYDASTLLPVHRGVGILRPDGEMGSDVLATTVRTYYLPNPDWRTICARGRALRESAGTLAGHAAGDDSAGSVDSASVARAVGDRSEGWVVELPEPLASVVDHLGDELHSREFVPSAELVEALEVEAGRFAREMGELGCRPLRQYVPDGDGVRRVRGYLTSEIRAAVDEIGSGSEAG
>NZ_CP023445.1|WP_096495563.1|5333519_5334146_-|hypothetical-protein
MSEPVERVARQVDRLCWTGILLGLAFTMTNVQQFAAAGAATWSLVWCAAWLLDPMVSLVLLAILRAEQVTAQRGVRMGGWVRTAKWFTLGATYVMNTWSAFTAGSAASVVLHSVPPLVVFVAAEAVTELRGKLGAVVVAAVPSGSLPVAKPPARPVRRTSFSEYLAVAEAARTPDVVVTPAWVRQVTGCSRGLSSRLAAVLNQGGGRS
>NZ_CP023445.1|WP_096495564.1|5334142_5334463_-|hypothetical-protein
MNGLTSAQVAGVVGVLLVLLFVWRAGARRARATARAAQAGVRLVSLAGRVLVNAAVIVLVQWVVITYRGSGWLLFGVLVVPALFAAHTLTRALTVTTYEPRRGGRR
>NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator
MNLVGIAWALDLLRWVPTGVLVAVVEWDGLCWAAEDLPPWDGELLTDRELAARMCAGCPVADECLELELRTGGEFGVGVWGGLCEQDRRELFPHWLRRGERWERP
>NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein
MSASGRCVEYTVRQAAWLLGVPRSTVSGAIRRGRLRVVWRRGRLVVPAPVVVRLLGGGR
>NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator
MSEDWAAVARAINQRVNELGWRQRELAERSNVSQAIVREIQHHTVERRRSPRTLESLSTALGLHPTHLEALLHNRTPPAADEPVTDPADSLWSRLDSVEQRLSDITDRLDGLKSDLSTVIEHVRDRR
>NZ_CP023445.1|WP_096495568.1|5335636_5337184_+|transcriptional-regulator
MALNEPWTGRTACALQSALRLSNEAFAEHLGIAPRTVAAWHQKPDLKPRSEMQQLLDTAHARADEAAQSRFTALTTTTLDLPEGAAADAELRLTTDSTIAAALEWLDQHAAWEPGTARREVATRLAHLDVPALHDRGARRSRVDQHATARALADYYGATPNHGRYTARFGTTTASTTILTRPEWLDLDCPLTTAHDRLKLTAVTPTQPPAMDQETAGRAAQRLAEALALGNRMVNMPLFRLLDVDVSKHAIGGTLGVTSFVEYAVTVDLLEAELSDALTTGTPTPLRDTYLPDLPAVLNVADRLCAGGTLALTAIARPADPFRGPADYLLLIQERSGHVINAARRLAVIPKGFHQPLTDFRADAQIGATLRRELEEELFGRDDIDNTVGEQRHADPMHPSRLSDPMRWLLLTPDRLRVECTGFGLNLVSGNFEFASLVVINDDEFWTRYGGEVQANWESASLRRYSSRDGDLLQELASDAAWSNEGLFALLQGLRRLREIGGERVDVPPIEWETQ
>NZ_CP023445.1|WP_096495569.1|5337168_5337528_+|signal-peptidase-I
MGDAVSNWQAGNVTEDASDTRGWLVGHFIAPAQGVRSQKDVEVKWFHHPAGDKRAEWTSDDQRTTLVFLISGNFRVDLTEGGKTMTEQGDYIMWGPGIDHSWEALADSVVMTVRWPSQT
>NZ_CP023445.1|WP_096497934.1|5337516_5338836_-|transcriptional-regulator
MKGDAVRSISRVEQPARSDVDFAVALDWLDGRAGWAAGTSRVKVRARMAEVDAEDLLDRRWGRAQVRREQLVRELMTYYGQPVGGDRLVSAVIEGWEVATTILSRTEWLRTPWLLDSGAGRMDFVGGGYQPRESLSAVAAGAAVDRLAEAAALGVRLTNLPLYRLVEAPAWEQGGGVVGTVPFAEYALTGDLLENELVDAVAARRGGLPLRDEYLPDLDSVLDVDNRVCAGGVLALCAIARPADRFRGPADYALLVQERSGSVLNAAGRLAVIPKGFHQPLNDLRGDASIRATLVREMEEELFGRCEVDTTLGGVRAAAPMHPGRCSEPMRWLTAEPERLRLECTGFGFNLVSGNYEFAGLVVIEDEEFWPRFGGQVEANWEAAGLRLYSSLDSDLITELVRDEAWSNEGLFALLQGLRRLREIGGQRVDLPSVEFSGL

Crispr_ID: NZ_CP023445_9

• CRISPR_ID: NZ_CP023445_9
• CRISPR_location: 5327228-5327381
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP023445_9

Consensus_repeat	Method
GCGGGTGGTGCCGCCGAGCGGGTCGGTC	CRISPRCasFinder

spacers of NZ_CP023445_9

>9.1|5327256|35|NZ_CP023445|CRISPRCasFinder
ACGGCGAGCAGCTGCTCCCGCTCGCCCCACTCGCG
>9.2|5327319|35|NZ_CP023445|CRISPRCasFinder
TCGCGGATGACCCGACCGCGCTCGTCGAGGTCGTA

CRISPR arrays and Neighbor proteins around NZ_CP023445_9

CRISPR arrays

The CRISPR arrays of NZ_CP023445_9

>merge|NZ_CP023445|9|5327228-5327381|CRISPRCasFinder
GCGGGTGGTGCGCCCGAGCGGGTCGGTGACGGCGAGCAGCTGCTCCCGCTCGCCCCACTCGCGGCTGGTGACCGCCCCGAGCGGGTTGGTCTCGCGGATGACCCGACCGCGCTCGTCGAGGTCGTAGGTGGTGGAGTTGCCGAGGGTGTCGGTG

>NZ_CP023445|9|8|5327228-5327381|CRISPRCasFinder
GCGGGTGGTGCGCCCGAGCGGGTCGGTG	ACGGCGAGCAGCTGCTCCCGCTCGCCCCACTCGCG
GCTGGTGACCGCCCCGAGCGGGTTGGTC	TCGCGGATGACCCGACCGCGCTCGTCGAGGTCGTA
GGTGGTGGAGTTGCCGAGGGTGTCGGTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl|CDD|270703
NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein	unknown	unknown	gnl|CDD|377856
NZ_CP023445.1|WP_096495563.1|5333519_5334146_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495554.1|5319150_5320410_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495559.1|5324343_5324823_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK	unknown	unknown	gnl|CDD|224588
NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein	unknown	unknown	gnl|CDD|340861
NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_CP023445.1|WP_096495564.1|5334142_5334463_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497934.1|5337516_5338836_-|transcriptional-regulator	unknown	unknown	unknown
NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376791
NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein	unknown	unknown	gnl|CDD|223314
NZ_CP023445.1|WP_157767790.1|5323622_5323997_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495568.1|5335636_5337184_+|transcriptional-regulator	unknown	unknown	unknown
NZ_CP023445.1|WP_096495558.1|5324003_5324357_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein	unknown	unknown	gnl|CDD|380454
NZ_CP023445.1|WP_096495569.1|5337168_5337528_+|signal-peptidase-I	unknown	unknown	unknown
NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein	unknown	unknown	gnl|CDD|223609

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein	gnl|CDD|270703	cd05154, ACAD10_11_N-like, N-terminal domain of Acyl-CoA dehydrogenase (ACAD) 10 and 11, and similar proteins. This subfamily is composed of the N-terminal domains of vertebrate ACAD10 and ACAD11, and similar uncharacterized bacterial and eukaryotic proteins. ACADs are a family of flavoproteins that are involved in the beta-oxidation of fatty acyl-CoA derivatives. ACAD deficiency can cause metabolic disorders including muscle fatigue, hypoglycemia, and hepatic lipidosis. There are at least 11 distinct ACADs, some of which show distinct substrate specificities to either straight-chain or branched-chain fatty acids. ACAD10 is widely expressed in human tissues and highly expressed in liver, kidney, pancreas, and spleen. ACAD10 and ACAD11 are both significantly expressed in human brain tissues. They contain a long N-terminal domain with similarity to phosphotransferases with a Protein Kinase fold, which is absent in other ACADs. They may exhibit multiple functions in acyl-CoA oxidation pathways. ACAD11 utilizes substrates with carbon chain lengths of 20 to 26, with optimal activity towards C22CoA. ACAD10 may be associated with an increased risk in type II diabetes. The ACAD10/11-like subfamily is part of a larger superfamily that includes the catalytic domains of other kinases, such as the typical serine/threonine/tyrosine protein kinases (PKs), RIO kinases, actin-fragmin kinase (AFK), and phosphoinositide 3-kinase (PI3K).	7.07188e-19
NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein	gnl|CDD|377856	pfam07508, Recombinase, Recombinase. This domain is usually found associated with pfam00239 in putative integrases/recombinases of mobile genetic elements of diverse bacteria and phages.	6.13554e-15
NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator	gnl|CDD|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	6.96793e-08
NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein	gnl|CDD|223609	COG0535, COG0535, Predicted Fe-S oxidoreductases [General function prediction only].	5.35451e-24
NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	0.000284351
NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein	gnl|CDD|380454	cd19531, LCL_NRPS-like, LCL-type Condensation (C) domain of non-ribosomal peptide synthetases(NRPSs) and similar domains including the C-domain of SgcC5, a free-standing NRPS with both ester- and amide- bond forming activity. LCL-type Condensation (C) domains catalyze peptide bond formation between two L-amino acids, ((L)C(L)). C-domains of NRPSs catalyze peptide bond formation within (usually) large multi-modular enzymatic complexes. NRPS can use a large variety of acyl monomers (approximately 500 different possible monomer substrates as opposed to the 20 standard amino acids in ribosomal protein synthesis) to construct bioactive secondary metabolites of 2 to 18 units long (with various activities such as antibiotic, antifungal, antitumor and immunosuppression). In addition to the LCL-type, there are various subtypes of C-domains such as the DCL-type which links an L-amino acid to the D-amino acid at the end of a growing peptide, starter C-domains which acylate the first amino acid with a beta-hydroxy carboxylic acid, and heterocyclization (Cyc) domains which catalyze both peptide bond formation and cyclization of Cys, Ser, or Thr residues. Typically, an NRPS module consists of an adenylation domain, a peptidyl carrier protein (PCP) domain (also known as thiolation (T) domain) and a C-domain. NRPS modules may also include specialized domains such as the terminal-module thioesterase (Te) domain that releases the product via hydrolysis or macrocyclization and any of various C-domain family members such as the epimerization (E) domain, the ester-bond forming C-domain, dual E/C (epimerization and condensation) domains, and the X-domain. Streptomyces globisporus SgcC5 is a free-standing NRPS condensation enzyme (rather than a modular NRPS), which catalyzes the condensation between the SgcC2-tethered (S)-3-chloro-5-hydroxy-beta-tyrosine and (R)-1phenyl-1,2-ethanediol, forming an ester bond, during the synthesis of the chromoprotein enediyne antitumor antibiotic C-1027. It has some acceptor substrate promiscuity as it has been shown to also catalyze the formation of an amide bond between SgcC2-tethered (S)-3-chloro-5-hydroxy-beta-tyrosine and a mimic of the enediyne core acceptor substrate having an amine at its C-2 position. C-domains typically have a conserved HHxxxD motif at the active site; mutations in this motif can abolish or diminish condensation activity. An HHxx[SAG]DGxSx(6)[ED] motif is characteristic of LCL-type C-domains.	5.9327e-40
NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK	gnl|CDD|224588	COG1674, FtsK, DNA segregation ATPase FtsK/SpoIIIE and related proteins [Cell division and chromosome partitioning].	6.62921e-13
NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.33471e-41
NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein	gnl|CDD|340861	cd17507, GT28_Beta-DGS-like, beta-diglucosyldiacylglycerol synthase and similar proteins. beta-diglucosyldiacylglycerol synthase (processive diacylglycerol beta-glucosyltransferase EC 2.4.1.315) is involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. This family of glycosyltransferases also contains plant major galactolipid synthase (chloroplastic monogalactosyldiacylglycerol synthase 1 EC 2.4.1.46). 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. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common 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.	1.84673e-06
NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000177543
NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein	gnl|CDD|223314	COG0236, AcpP, Acyl carrier protein [Lipid metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	4.29477e-06

Protein sequences

>NZ_CP023445.1|WP_096495559.1|5324343_5324823_-|hypothetical-protein
MTPAWADRLLPADAALLARCFPGGRAGLSGSLLRSVRLDRVGPACSLRLDLPGDGPGATQAHLGMLAVADVELAGGALPQRVDVEITDLPGRRVAVVVAGGGLRLSLTCAEVLRFGRVSDHDTPPGAVDDGPHRFVGRLDQRLHRVVPGPEDENYHARF
>NZ_CP023445.1|WP_096495558.1|5324003_5324357_-|hypothetical-protein
MPASDDFPGDFPGDLDALHWDERGDAVTATFEAGLDDAGRAAWGAEAGHTRVRYHVRFAGVADLRVAGFDHRLPLRLAVIADGARVGVEVSGAGTDVRFTSAPPEHVGHRTFTAAAP
>NZ_CP023445.1|WP_157767790.1|5323622_5323997_+|hypothetical-protein
MLRTTSRAAMTGFAILALAGAGAGSATAVERELTTIAVPPLQPAGGEVKASSVACVWKYSPGRNPTVWVDCHQVGGGAATGFEVTVTCSDGSSHTSGATRFGSPAMAYCPGATTMKSFTLSAHY
>NZ_CP023445.1|WP_096495556.1|5322156_5323512_+|hypothetical-protein
MPRTWPASPFQHTIMTNDGTIPSGSTGPHMTMSISALVTGGLDVDLLDAAYDDLVARNDVLRTTLEPDGEQWRQRVHPHRTAHLHRAEAAAPEAQSFVDAWSREPVPIDRPPLVRGQVVALDDGSHLVNLVFHHVHTDPPSLVLAVAELGALYTARLAGEPLPPPPLQYGPYSARRAAITAPTLDADLDHWRTTVEGARPLDLSPSRDLSTPPDSGVLRLDVLDGRDAAALEKWALRRRTTVFATLFTAFCLAAADRSTTRDVLVNTVFEQRAHPDVRTLIGPFLHPSVLRVRVPEGATWSSMTPVVREAVGAAYARAHVPGFDVLRLHPDVIHAVETEPVGLCVFQYLPYSGLEDTFAYGPATARVLARTQAGPTGDVGLMFRLHRRSSGSLYATVTYDRRDLTEPVVRALFTDFTTRLREPLAERAPRTGSPSRPRDTAAPQRDSAPVT
>NZ_CP023445.1|WP_096495555.1|5320705_5321881_-|radical-SAM-protein
MHPRTARTLNQKEFHDLRRTVAIRAETRRNIEVDATYATPLPREVSLQLTYKCNLRCNHCYQWNDQGFFHDFSKVKQRTELDLDIVDDVLRMTDDTRAKVFLWGGEPLMHSRFGEVAELLARTPRTVNLCTNALLVKRNLEHLLTIGPGLNVLVSLDGLGADHEALRGKGTFPRTIDNVRLLLDLQKSGEYQGEVSLSCMVSNETVGSMREFMEWAEELGVNSVYFQFPWFISPEVASAMDDMYAENFAWLNPPAPGTTPTWHSYTYRIEPGLIDTLWRSMAELAERTWNVRIRYQPQLEPDEVEDFVLGTSRPAQKRNRCLAVSNRLEVHADGKVSSCKFFPEFVIGDLHESGVAEVWQGEAFRRVRSVLRGTSLMPVCSKCILLYLNGV
>NZ_CP023445.1|WP_096497933.1|5320406_5320649_-|D-alanyl-carrier-protein
MRIKEVLAGVLGAPELVERITDATNVVQDLGINSIQMINFLLALEDAFDVELEFEELSFEQLESLPEIRRFVVAAMPDSP
>NZ_CP023445.1|WP_096495554.1|5319150_5320410_-|hypothetical-protein
MTGARALRLGAFDVERRWRPDGLAALPEIVDRGADVVASAMDELLAVACGPGDVLVTGAPVPVAWHEVLAGAGIGFEHRVAPGGVGGSVEQRLVARPPADLGGLGFEPYAVLPESAGVVGALGLRAELPDWRVVRAVSSKSWSNALVRELGLAGAGVVVDSVAGLQAQVEALDGAPALLKDPFGVSGRGTLALTSPLVLRSVVRVLDKQVRRGLDVEVLVQRRFDPVADFSAQFSVRPGGRVDWLGTRLIENTGFAYAGSRPAPPWLAERLSALGYREIMADVGAALAGAGYRGPVCVDSMLLRDGTLVPVLEINPRTSMGLISVLAGRRLAADPERARLVVRPVRGGAGFDRLVALLRADGVLLEAGGGGVLPLSSGTLASSRGRLYCAVVARDEAGHRALGAALDAVLGAWQVDRAS
>NZ_CP023445.1|WP_096495553.1|5318165_5319161_-|Gfo/Idh/MocA-family-oxidoreductase
MPRELGLIGATAIAVRAVLDPARRREDVRVRAIAASTPERAEAFRAEHGLPVAHADYRSLVRDEGIDTVYVSLHNSAHARWAAEAARAGKHVVVEKPLCLGRREAHALRRAAGDAGVHVVEAVITTGHPWQAAVRELVASRELGELTGISSHIAFDLPPGAGYRFRPELGGGAFHDTASYWLDAVQAVVGLGGATASGHSEFSGPNGVDLEFDAALRLPSGVRAELRASLVGPYRADHEFRFTGGKARLRNFLRPAAGPFPVNLVLQRDGGAREVRSFPAVSYYDAQFDRIMALLARPARPDDAVVERITVLESAYLNALERCARTGRAEA
>NZ_CP023445.1|WP_096497932.1|5317101_5318163_-|hypothetical-protein
MAVLTSGVALGVHVPGLLLARRLAEVGVAARVDVLENHLPERLRELIPASKTAFHRDFRVALAGQRLAARNTTEPDEGLVAGLWREWERDGVELLVVLSGFWLPTAHRYASAHSGVRVRSCHVDSVASPSFTSASGAGRGRWGEHEDVWLLERAGSAVARTIPVSREEPEPWGDRDGRLLAHGGGWGMGTYRTGAAELGAAGFALDVVAYERSEVPEEQGRNRYFMIDPDWHPWHDTGFPPFGRVHDGAVEYRRRAEHHDGFDLTRRAIAVVSKPGGGTLMDSLSAATPVVLLEPFGAHEARNAELWRDLGFGIGYREWVDGGRQVAVLEALHRNLVAARGRVLSYPDELAGR
>NZ_CP023445.1|WP_096495552.1|5316068_5317070_+|aminoglycoside-phosphotransferase-family-protein
MRSTTKRSLSDEELRAAVTEAFGPRATITSSRELADGTFNAVWLLDVDPVGPVVLKAAPPDDLPLLTYERRIARTEAAVLRAAAATAPVPVLHHAGEGSAGVGGDFLITSVVEGDTWQRVSGELGGAERARLRRELGRAVAGLHAVRGTAFGYPERSTGLHGGTWYEAFTAMVDGLLADARRFGVTPPGRPTALHDLAVAGRALLEEVTEPVLVHFDLWNGNVMLTGEEGERRLSGLIDLERAFWGDPCADFVSLALLGELSDDDPLLDGYREAGGPAQLTATTRRRIALYQAYLYLIMIVEAVPRGHKGVKSAAAQALFRSRYRRALRRAAP
>NZ_CP023445.1|WP_096495561.1|5329596_5331360_-|recombinase-family-protein
MTVEISRDPWETLDRLLGVEVAEAVGDGIGAVAFYGRCSTEDNQDPETSHGWQLGNARKFVEPLGGHVVVEFFDVGQSRSVPWERRPEAARLLAQLKNPQRGWSALVVGEGTRCWFGNQFSLIAPRFAAYGVELWVPELGGRFEPRNPSHKMLMSVLGGMSESERQHVQARVRAAMDSQVVNEGRHQGGRAPYGYVVVDGGPHPNPRKAAEGYRLRKLAVEEASAEVVRRIFAEYLSGRGDRAIATGLNRDAVPCPSARRPDQNPHRLADGWQGSTVRAILDNPRYTGFAFFGRWTRQEMLLDPDDVAAGHVVRFRRATADKVVRSRKPAHPAIVGVEEFTQVQLLRKSKSAGGLKTARKAERSERPTKRPYLFRGRVRCTICGRKMEASPRARGVYYRCPARTLAPGAPALAEHPPTVYLREDVLQDAVNGWLGGLFAPQNLDRTVAALVASQEGAAGKGDSREAARLRLSKAEEQLSRFQEAIKAGIDPLALVEAVNEAQAVRTAAKAELEGLPVPNLLGAAEVHAMIDSLGNVGAALKGAGIERVAGLYTAVDLQVRYTHTARRADVIIKPAGCVNNVRVRGGT
>NZ_CP023445.1|WP_096495562.1|5331498_5333523_-|cell-division-protein-FtsK
MNGDLVHVEPVLVGEVVAEPAALVRLVPVAWRSRQAWRDVAIRLLRLPLRFFPAVGRGALVVFRAWRRWVRVRDYREAAEQAEKLADKYVEIRELGLYRWRVTGMVLGLVSALLFAGHVVWGGVLLWGVAGGGAAVVAVIGRRKDGSPGRKAVLDGSRVLAWTMDAQLLVDAFRDAKLIGKDETLRLVERPHRVGDGWAVVADLPATRKAVDVIKNRDALASALAVDEVQLVAERVRGRGGHAGRVSLWVADEDPYAGAPLRAPLLDVERWDAWRAVPFGRDARGRRVDLPLVWTSLLVGAIPRQGKTFATRLAVSGFVLDPYARLYVFDGKGGKDWEAAEQIAYRYVCGDEQEHAEAVRDHLVALVAEVQERYARMATVDDELCPESKITPALSRDPDLGMPVTGVVIDEVQVYLENTARVEVGGRKTTLGLYVADLLTYLVRKGPAAGIVVVLATQRPDSNTIPSRLRAVLGSRFALRVMDWRDSNIVLGEQMNTRGYDASTLLPVHRGVGILRPDGEMGSDVLATTVRTYYLPNPDWRTICARGRALRESAGTLAGHAAGDDSAGSVDSASVARAVGDRSEGWVVELPEPLASVVDHLGDELHSREFVPSAELVEALEVEAGRFAREMGELGCRPLRQYVPDGDGVRRVRGYLTSEIRAAVDEIGSGSEAG
>NZ_CP023445.1|WP_096495563.1|5333519_5334146_-|hypothetical-protein
MSEPVERVARQVDRLCWTGILLGLAFTMTNVQQFAAAGAATWSLVWCAAWLLDPMVSLVLLAILRAEQVTAQRGVRMGGWVRTAKWFTLGATYVMNTWSAFTAGSAASVVLHSVPPLVVFVAAEAVTELRGKLGAVVVAAVPSGSLPVAKPPARPVRRTSFSEYLAVAEAARTPDVVVTPAWVRQVTGCSRGLSSRLAAVLNQGGGRS
>NZ_CP023445.1|WP_096495564.1|5334142_5334463_-|hypothetical-protein
MNGLTSAQVAGVVGVLLVLLFVWRAGARRARATARAAQAGVRLVSLAGRVLVNAAVIVLVQWVVITYRGSGWLLFGVLVVPALFAAHTLTRALTVTTYEPRRGGRR
>NZ_CP023445.1|WP_096495565.1|5334459_5334777_-|WhiB-family-transcriptional-regulator
MNLVGIAWALDLLRWVPTGVLVAVVEWDGLCWAAEDLPPWDGELLTDRELAARMCAGCPVADECLELELRTGGEFGVGVWGGLCEQDRRELFPHWLRRGERWERP
>NZ_CP023445.1|WP_096495566.1|5334773_5334953_-|helix-turn-helix-domain-containing-protein
MSASGRCVEYTVRQAAWLLGVPRSTVSGAIRRGRLRVVWRRGRLVVPAPVVVRLLGGGR
>NZ_CP023445.1|WP_096495567.1|5335117_5335501_+|helix-turn-helix-transcriptional-regulator
MSEDWAAVARAINQRVNELGWRQRELAERSNVSQAIVREIQHHTVERRRSPRTLESLSTALGLHPTHLEALLHNRTPPAADEPVTDPADSLWSRLDSVEQRLSDITDRLDGLKSDLSTVIEHVRDRR
>NZ_CP023445.1|WP_096495568.1|5335636_5337184_+|transcriptional-regulator
MALNEPWTGRTACALQSALRLSNEAFAEHLGIAPRTVAAWHQKPDLKPRSEMQQLLDTAHARADEAAQSRFTALTTTTLDLPEGAAADAELRLTTDSTIAAALEWLDQHAAWEPGTARREVATRLAHLDVPALHDRGARRSRVDQHATARALADYYGATPNHGRYTARFGTTTASTTILTRPEWLDLDCPLTTAHDRLKLTAVTPTQPPAMDQETAGRAAQRLAEALALGNRMVNMPLFRLLDVDVSKHAIGGTLGVTSFVEYAVTVDLLEAELSDALTTGTPTPLRDTYLPDLPAVLNVADRLCAGGTLALTAIARPADPFRGPADYLLLIQERSGHVINAARRLAVIPKGFHQPLTDFRADAQIGATLRRELEEELFGRDDIDNTVGEQRHADPMHPSRLSDPMRWLLLTPDRLRVECTGFGLNLVSGNFEFASLVVINDDEFWTRYGGEVQANWESASLRRYSSRDGDLLQELASDAAWSNEGLFALLQGLRRLREIGGERVDVPPIEWETQ
>NZ_CP023445.1|WP_096495569.1|5337168_5337528_+|signal-peptidase-I
MGDAVSNWQAGNVTEDASDTRGWLVGHFIAPAQGVRSQKDVEVKWFHHPAGDKRAEWTSDDQRTTLVFLISGNFRVDLTEGGKTMTEQGDYIMWGPGIDHSWEALADSVVMTVRWPSQT
>NZ_CP023445.1|WP_096497934.1|5337516_5338836_-|transcriptional-regulator
MKGDAVRSISRVEQPARSDVDFAVALDWLDGRAGWAAGTSRVKVRARMAEVDAEDLLDRRWGRAQVRREQLVRELMTYYGQPVGGDRLVSAVIEGWEVATTILSRTEWLRTPWLLDSGAGRMDFVGGGYQPRESLSAVAAGAAVDRLAEAAALGVRLTNLPLYRLVEAPAWEQGGGVVGTVPFAEYALTGDLLENELVDAVAARRGGLPLRDEYLPDLDSVLDVDNRVCAGGVLALCAIARPADRFRGPADYALLVQERSGSVLNAAGRLAVIPKGFHQPLNDLRGDASIRATLVREMEEELFGRCEVDTTLGGVRAAAPMHPGRCSEPMRWLTAEPERLRLECTGFGFNLVSGNYEFAGLVVIEDEEFWPRFGGQVEANWEAAGLRLYSSLDSDLITELVRDEAWSNEGLFALLQGLRRLREIGGQRVDLPSVEFSGL

Crispr_ID: NZ_CP023445_10

• CRISPR_ID: NZ_CP023445_10
• CRISPR_location: 6009605-6009815
• CRISPR_type: Orphan
• Repeat_type: I-C,I-E,II-B
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP023445_10

Consensus_repeat	Method
GTCTTCCCCGCACATGCGGGGGTGGTCC	PILER-CR
GTCTTCCCCGCACATGCGGGGGTGGTCC	CRISPRCasFinder
GTCTTCCCCGCACATGCGGGGGTGGTCC	CRT

spacers of NZ_CP023445_10

>10.1|6009633|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT
GGGGCACCCGCGTGCGGGGAAGCGTCGGTTCAA
>10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT
CGTCGCAGCGGCCTCGATCAGGTCCACGACCTG
>10.3|6009755|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT
GTACTTGTCCCCCAAACCACGCCCGACGTGCAG

CRISPR arrays and Neighbor proteins around NZ_CP023445_10

CRISPR arrays

The CRISPR arrays of NZ_CP023445_10

>merge|NZ_CP023445|10|6009605-6009815|PILER-CR,CRISPRCasFinder,CRT
GTCTTCCCCGCACATGCGGGGGTGGTCCGGGGCACCCGCGTGCGGGGAAGCGTCGGTTCAAGTCTTCCCCGCACATGCGGGGGTGGTCCCGTCGCAGCGGCCTCGATCAGGTCCACGACCTGGTCTTCCCCGCACATGCGGGGGTGGTCCGTACTTGTCCCCCAAACCACGCCCGACGTGCAGGTCTTCCCCGCACATGCGGGGGTAGTCC

>NZ_CP023445|10|1|6009605-6009815|PILER-CR
GTCTTCCCCGCACATGCGGGGGTGGTCC	GGGGCACCCGCGTGCGGGGAAGCGTCGGTTCAA
GTCTTCCCCGCACATGCGGGGGTGGTCC	CGTCGCAGCGGCCTCGATCAGGTCCACGACCTG
GTCTTCCCCGCACATGCGGGGGTGGTCC	GTACTTGTCCCCCAAACCACGCCCGACGTGCAG
GTCTTCCCCGCACATGCGGGGGTAGTCC

>NZ_CP023445|10|9|6009605-6009815|CRISPRCasFinder
GTCTTCCCCGCACATGCGGGGGTGGTCC	GGGGCACCCGCGTGCGGGGAAGCGTCGGTTCAA
GTCTTCCCCGCACATGCGGGGGTGGTCC	CGTCGCAGCGGCCTCGATCAGGTCCACGACCTG
GTCTTCCCCGCACATGCGGGGGTGGTCC	GTACTTGTCCCCCAAACCACGCCCGACGTGCAG
GTCTTCCCCGCACATGCGGGGGTAGTCC

>NZ_CP023445|10|2|6009605-6009815|CRT
GTCTTCCCCGCACATGCGGGGGTGGTCC	GGGGCACCCGCGTGCGGGGAAGCGTCGGTTCAA
GTCTTCCCCGCACATGCGGGGGTGGTCC	CGTCGCAGCGGCCTCGATCAGGTCCACGACCTG
GTCTTCCCCGCACATGCGGGGGTGGTCC	GTACTTGTCCCCCAAACCACGCCCGACGTGCAG
GTCTTCCCCGCACATGCGGGGGTAGTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096497996.1|6004661_6006524_-|4-alpha-glucanotransferase	unknown	unknown	gnl|CDD|237737
NZ_CP023445.1|WP_096496021.1|6004218_6004557_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496019.1|5999685_6001935_-|malto-oligosyltrehalose-synthase	unknown	unknown	gnl|CDD|200475
NZ_CP023445.1|WP_096496029.1|6018652_6019393_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187585
NZ_CP023445.1|WP_096497998.1|6016052_6016871_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP023445.1|WP_096496025.1|6011400_6013482_-|penicillin-binding-protein	unknown	unknown	gnl|CDD|223815
NZ_CP023445.1|WP_015803832.1|6014880_6015612_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|236607
NZ_CP023445.1|WP_096496024.1|6008464_6009415_-|LLM-class-F420-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274812
NZ_CP023445.1|WP_041837014.1|6016922_6017108_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP023445.1|WP_096497999.1|6019430_6020195_-|DeoR/GlpR-transcriptional-regulator	unknown	unknown	gnl|CDD|224268
NZ_CP023445.1|WP_096496027.1|6017112_6017667_+|nucleotidyltransferase-family-protein	unknown	unknown	gnl|CDD|133025
NZ_CP023445.1|WP_015803820.1|5997356_5997848_+|ANTAR-domain-containing-protein	unknown	unknown	gnl|CDD|377145
NZ_CP023445.1|WP_096496018.1|5997796_5999689_-|malto-oligosyltrehalose-trehalohydrolase	unknown	unknown	gnl|CDD|274114
NZ_CP023445.1|WP_096496028.1|6017659_6018556_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|182183
NZ_CP023445.1|WP_096496026.1|6013824_6014868_-|carbohydrate-kinase-family-protein	unknown	unknown	gnl|CDD|238917
NZ_CP023445.1|WP_096497997.1|6009942_6010701_-|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|366703
NZ_CP023445.1|WP_096496020.1|6001931_6004058_-|glycogen-debranching-protein-GlgX	unknown	unknown	gnl|CDD|131155
NZ_CP023445.1|WP_096496022.1|6006929_6007892_-|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP023445.1|WP_096496023.1|6008002_6008461_+|peroxiredoxin	unknown	unknown	gnl|CDD|239315
NZ_CP023445.1|WP_084799265.1|5996897_5997065_-|CsbD-family-protein	unknown	unknown	gnl|CDD|283241

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096497996.1|6004661_6006524_-|4-alpha-glucanotransferase	gnl|CDD|237737	PRK14507, PRK14507, malto-oligosyltrehalose synthase.	1.96354e-147
NZ_CP023445.1|WP_096496019.1|5999685_6001935_-|malto-oligosyltrehalose-synthase	gnl|CDD|200475	cd11336, AmyAc_MTSase, Alpha amylase catalytic domain found in maltooligosyl trehalose synthase (MTSase). Maltooligosyl trehalose synthase (MTSase) domain. MTSase and maltooligosyl trehalose trehalohydrolase (MTHase) work together to produce trehalose. MTSase is responsible for converting the alpha-1,4-glucosidic linkage to an alpha,alpha-1,1-glucosidic linkage at the reducing end of the maltooligosaccharide through an intramolecular transglucosylation reaction, while MTHase hydrolyzes the penultimate alpha-1,4 linkage of the reducing end, resulting in the release of trehalose. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_CP023445.1|WP_096496029.1|6018652_6019393_+|SDR-family-oxidoreductase	gnl|CDD|187585	cd05324, carb_red_PTCR-like_SDR_c, Porcine testicular carbonyl reductase (PTCR)-like, classical (c) SDRs. PTCR is a classical SDR which catalyzes the NADPH-dependent reduction of ketones on steroids and prostaglandins. Unlike most SDRs, PTCR functions as a monomer. This subgroup also includes human carbonyl reductase 1 (CBR1) and CBR3. CBR1 is an NADPH-dependent SDR with broad substrate specificity and may be responsible for the in vivo reduction of quinones, prostaglandins, and other carbonyl-containing compounds. In addition it includes poppy NADPH-dependent salutaridine reductase which catalyzes the stereospecific reduction of salutaridine to 7(S)-salutaridinol in the biosynthesis of morphine, and Arabidopsis SDR1,a menthone reductase, which catalyzes the reduction of menthone to neomenthol, a compound with antimicrobial activity; SDR1 can also carry out neomenthol oxidation. 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, 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) 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.	5.20725e-85
NZ_CP023445.1|WP_096497998.1|6016052_6016871_+|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	3.17723e-27
NZ_CP023445.1|WP_096496026.1|6013824_6014868_-|carbohydrate-kinase-family-protein	gnl|CDD|238917	cd01942, ribokinase_group_A, Ribokinase-like subgroup A. Found in bacteria and archaea, this subgroup is part of the ribokinase/pfkB superfamily. Its oligomerization state is unknown at this time.	1.28438e-56
NZ_CP023445.1|WP_015803832.1|6014880_6015612_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|236607	PRK09648, PRK09648, RNA polymerase sigma factor ShbA.	1.52052e-72
NZ_CP023445.1|WP_096496024.1|6008464_6009415_-|LLM-class-F420-dependent-oxidoreductase	gnl|CDD|274812	TIGR03841, F420_Rv3093c, probable F420-dependent oxidoreductase, Rv3093c family. This model describes a small family of enzymes in the bacterial luciferase-like monooxygenase family, which includes F420-dependent enzymes such as N5,N10-methylenetetrahydromethanopterin reductase as well as FMN-dependent enzymes. All members of this family are from species that produce coenzyme F420; SIMBAL analysis suggests that members of this family bind F420 rather than FMN. [Unknown function, Enzymes of unknown specificity].	1.73528e-89
NZ_CP023445.1|WP_041837014.1|6016922_6017108_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	3.56138e-14
NZ_CP023445.1|WP_096497999.1|6019430_6020195_-|DeoR/GlpR-transcriptional-regulator	gnl|CDD|224268	COG1349, GlpR, Transcriptional regulators of sugar metabolism [Transcription / Carbohydrate transport and metabolism].	7.25171e-68
NZ_CP023445.1|WP_015803820.1|5997356_5997848_+|ANTAR-domain-containing-protein	gnl|CDD|377145	pfam03861, ANTAR, ANTAR domain. ANTAR (AmiR and NasR transcription antitermination regulators) is an RNA-binding domain found in bacterial transcription antitermination regulatory proteins. The majority of the domain consists of a coiled-coil.	2.12812e-11
NZ_CP023445.1|WP_096496025.1|6011400_6013482_-|penicillin-binding-protein	gnl|CDD|223815	COG0744, MrcB, Membrane carboxypeptidase (penicillin-binding protein) [Cell envelope biogenesis, outer membrane].	6.64035e-125
NZ_CP023445.1|WP_096496018.1|5997796_5999689_-|malto-oligosyltrehalose-trehalohydrolase	gnl|CDD|274114	TIGR02402, Malto-oligosyltrehalose_trehalohydrolase, malto-oligosyltrehalose trehalohydrolase. Members of this family are the trehalose biosynthetic enzyme malto-oligosyltrehalose trehalohydrolase, formally known as 4-alpha-D-{(1->4)-alpha-D-glucano}trehalose trehalohydrolase (EC 3.2.1.141). It is the TreZ protein of the TreYZ pathway for trehalose biosynthesis, and alternative to the OtsAB system. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP023445.1|WP_096496028.1|6017659_6018556_-|LysR-family-transcriptional-regulator	gnl|CDD|182183	PRK09986, PRK09986, LysR family transcriptional regulator.	4.15601e-38
NZ_CP023445.1|WP_096497997.1|6009942_6010701_-|peptidoglycan-DD-metalloendopeptidase-family-protein	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.	7.64767e-39
NZ_CP023445.1|WP_096496027.1|6017112_6017667_+|nucleotidyltransferase-family-protein	gnl|CDD|133025	cd04182, GT_2_like_f, GT_2_like_f is a subfamily of the glycosyltransferase family 2 (GT-2) with 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.	7.82905e-39
NZ_CP023445.1|WP_096496020.1|6001931_6004058_-|glycogen-debranching-protein-GlgX	gnl|CDD|131155	TIGR02100, Glycogen_operon_protein_GlgX_homolog, glycogen debranching enzyme GlgX. This family consists of the GlgX protein from the E. coli glycogen operon and probable equivalogs from other prokaryotic species. GlgX is not required for glycogen biosynthesis, but instead acts as a debranching enzyme for glycogen catabolism. This model distinguishes GlgX from pullanases and other related proteins that also operate on alpha-1,6-glycosidic linkages. In the wide band between the trusted and noise cutoffs are functionally similar enzymes, mostly from plants, that act similarly but usually are termed isoamylase. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP023445.1|WP_096496022.1|6006929_6007892_-|LacI-family-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.22994e-56
NZ_CP023445.1|WP_096496023.1|6008002_6008461_+|peroxiredoxin	gnl|CDD|239315	cd03017, PRX_BCP, Peroxiredoxin (PRX) family, Bacterioferritin comigratory protein (BCP) subfamily; composed of thioredoxin-dependent thiol peroxidases, widely expressed in pathogenic bacteria, that protect cells against toxicity from reactive oxygen species by reducing and detoxifying hydroperoxides. The protein was named BCP based on its electrophoretic mobility before its function was known. BCP shows substrate selectivity toward fatty acid hydroperoxides rather than hydrogen peroxide or alkyl hydroperoxides. BCP contains the peroxidatic cysteine but appears not to possess a resolving cysteine (some sequences, not all, contain a second cysteine but its role is still unknown). Unlike other PRXs, BCP exists as a monomer. The plant homolog of BCP is PRX Q, which is expressed only in leaves and is cellularly localized in the chloroplasts and the guard cells of stomata. Also included in this subfamily is the fungal nuclear protein, Dot5p (for disrupter of telomere silencing protein 5), which functions as an alkyl-hydroperoxide reductase during post-diauxic growth.	1.317e-52
NZ_CP023445.1|WP_084799265.1|5996897_5997065_-|CsbD-family-protein	gnl|CDD|283241	pfam05532, CsbD, CsbD-like. CsbD is a bacterial general stress response protein. It's expression is mediated by sigma-B, an alternative sigma factor. The role of CsbD in stress response is unclear.	1.93209e-07

Protein sequences

>NZ_CP023445.1|WP_096496024.1|6008464_6009415_-|LLM-class-F420-dependent-oxidoreductase
MGRWGITLPLTGVPILDHQPLVSELTALGYTDIWSAETSGADAFTPLALAAQWSPTARLGTAIAPVYTRGPALLAMSAATLAEVSGGRFVLGIGSSSPAIVSRWNGQEFTEPFARTRDTLRFLRSALAGDKVTREYPTFSVSGFRLEKAPAHHVPIMLAALRPGMLRLAAREADGAITNWLAATDVPRVREALGDKELAARIFVCPTEDADAARALGRALICAYLTVPAYAAFHDWLGRDKVLAPMREAWSAGRRKEANALVPDEVVDALVVHGSAEQCRARVAQYAANGVDTPIIGLLPTGGDQLDLVRRLAPGA
>NZ_CP023445.1|WP_096496023.1|6008002_6008461_+|peroxiredoxin
MKPGDQVSDFTLPDQDGEPRTLSALLADGPVVLFFYPSAMTSGCTAESCHFRDLAAEFAQAGAQRVGISTDSVARQKQFADINSFDYPLLSDADGAVAEAFGVKRRFGPLPVKRHTFVIGTDLTVLEVIKSEFAMNAHADKALAVLRERAGS
>NZ_CP023445.1|WP_096496022.1|6006929_6007892_-|LacI-family-transcriptional-regulator
MTSMSDVAKAAGVSAATVSRALRGEPGVSESTREHVAEVAKRMRYAIARDASSLAGGRRYAVAVLTADVGRGDLLAGAESALREAGYDVLLYVLNDPAARARFFDQVPTGRRVDGVLALATRPTEAERAALDGAGVPVVLVEDGDLGEAVALAARHLIGHGHREVALVLAEDVDESLDEVLAAEGLAVRPEWTVWSSPTVAGGEQVVDALLDGGALPTAVISSSGEVALGVYLRLRRDGREDVSVVSLEGAELARAVGITAVEGAWRERGEHATAVLLSALRGDAQPHAEAIAPPSAQLVVRGSSGPAPRSGATPPTVAP
>NZ_CP023445.1|WP_096497996.1|6004661_6006524_-|4-alpha-glucanotransferase
MDEDLAALARAHGVATWYEDAGDTRVEVDADVVVAVLAELGVDASTPEAVRAALAAPTPPPATIVLREGQLLEGDGTVVLEDGGSARLPAVLPLGYHRLGDRTVVVAPAKLPPVPRAWGWMLQLYAMRSEQSWGMGDYGDLATTARRSATELGAGVLLVNPVQAISPTHPVERSPYSPSSRRFANPLYLRVTDLEEFHRAPTEVRRAVVAQRPENADLIDYDAVWAAKKAALELLWADREHDLPEDPDLLDFARFCAIAERHGPDWRHWPADQRDPATATADPERVAFHAWLQTLCERQLADARAAASAMPVGIVHDLPVGVHPGGADTWALRDAFAAGVRVGAPPDAFNQLGQDWNLPPWRPDRLAEQGYEPFRAVLRGVLRHADGIRVDHVAGLWRLWWIPPGEPAKRGTYVHYDADAMLAVLTLEAHRAGAVVVGEDLGTVEDRVTEELHERGALSSAVLWFQRDYDQPGHPLIPPKGWTTSAMASVSTHDLPTLAGFLQAEHVRIRAELGLFEVDPKGEFEAAEAERDQLVELLRQEGVLGDDLLVSFHALLAEAPSVLVLTSPQDAVGETRQPNLPGTVDQYPNWRIPLPGGLDAFLTDPRVRAIAAALRAGRAR
>NZ_CP023445.1|WP_096496021.1|6004218_6004557_-|hypothetical-protein
MNTDLVTPTATAVIPAQLTTNPEDELELAVEKVLASVRPSSLGDPAEGSRRAERVLRDALDLPGEPTNEALRQARACAEAACEHLRYQEFQEARLLLVASRGQLARAHTGRA
>NZ_CP023445.1|WP_096496020.1|6001931_6004058_-|glycogen-debranching-protein-GlgX
MRPWPGTPYPLGATYDGVGTNFTLFSEAGEWVELCLFDDEGNEERVRLPEVDGFVHHGYLLGIGPGQRYGYRVHGPHQPEQGLRCNPNKLLIDPYAKAIDGEVKWHESLFGYPFGDPDARNDQDSAGHVPLSVVVNPFFDWANDRPPKIPYNETVIYEAHVRGLTMRHPEVPERLRGTYAGLAHPVVIDHLKKLGVNAIELMPVHQFVTDHGLVEKDLRNYWGYNTIGFFAPHDGYSALGHDAGQVQEFKGMVRALHEAGIEVILDVVYNHTAEGNHLGPTLSMRGIDNQAYYRLVEDEPKYYMDYTGTGNSMNVRSPHTLQLIMDSLRYWVTEMHVDGFRFDLAATLAREFYDVDRLSTFFDLVQQDPVVSQVKLIAEPWDVGPGGYQVGNFPPLWTEWNGKYRDTARDFWRGEPATLGEFASRFTGSSDLYKEDGRRPYASINFVTAHDGFTLTDLVSYNDKHNLANGEDGRDGADDNRSWNCGVEGPTDDPEVNELRERQRRNLLTTLLLSQGVPMLLHGDELGRTQQGNNNAYCQDNELSWVDWTLLEKNQPLLDFTSGLTDFRKKHPVFRRRRFFQGRPIRKGEELRDIAWFTPAGEEMTEQNWEDGFGRCVSVFLNGKGIPDLDQRGMKVEDDSFLVVFNAHHEDIEITLPGEGYGPEWAVVIDTATGEIAAFPQDEPTIPAGGSVTATARSVVVLQRMGAE
>NZ_CP023445.1|WP_096496019.1|5999685_6001935_-|malto-oligosyltrehalose-synthase
MTAPDRATAAPATAPATTAGAARPQPPSSTYRLQFTPDFTFADAEAVLDYLGALGAGALYASPLLEAVPGSTHGYDVTDPARARADFGGEQGRASLAKAVRAAGLGFVVDIVPNHMAVDSTPVNAWWTDVMEKGQGSPYARYFDIDWSDGTLLLPFAGDEGSEEEHEHYRLAFWRRGNAELNYRRFFDITTLAAVRVEDPEVFEATHGEVLRWVAEGDVTGLRVDHPDGLADPGGYARDLAARSGAWVVVEKILGPDESLPVSWPVAGTTGYDALREVCGLFVDPAGEGPFTDLAVELGVPTDFAAVEHECRALVASTILSAEVRRIAALLEPSLPEGVGAEQAREAVAAVMAAFPVYRSYLPEGEQDWATAVRRAGGPAAEALDAAVRADPTGELATRIQQTSGMVVAKGTEDTAFYRFTRFVALNEVGGAPDRFGVTPEEFHRRAAARESGSPDTMTALSTHDTKRSEDVRARLAVLAEVPDEFAAAVRRWSAAHPIDEPSLNALAWQSLVGAWPVTADRMRAYLEKAAKESKVRTTWVDHDEEFEAAVDAWPAAVLGSDTAGEVAEFVDGIVAAGWSNALGQKLVQLTAPGVPDVYQGTELWDLSLVDPDNRRPVDYAPRRALLERIDSGWLPDVDDSGAAKLLVTSRALRLRGQRPELFRGYRPVPAAGPASAHALAFERTGLITVATRLPVGLARAGGWGSTVLPLPPGEWTDVLTGRVVTGSAPALADLLDRYPVALLVRGDR
>NZ_CP023445.1|WP_096496018.1|5997796_5999689_-|malto-oligosyltrehalose-trehalohydrolase
MTFSVWAPDRDGVVVRVDGQDHDMTPVGGGWWYSDASGTDYAFVLDGDALPDPRSLRQPDGVHGPSRAYDHDEFAWTDQRWTGRALPGAVVYELHVGTFTPGGTFDSAVERLDHLADLGITHVEVLPVNSFDGPSGWGYDGVLWGAVHEPYGGPDGFKRFVDACHARGLAVLLDVVYNHLGPSGAYLDRFGPYFAGSNEWGPGLNLDGPGSDEVRRYVVDNALGWLRDFHVDGLRLDAVHALLDRSATHLLEQLAREVDALSTALGRPLTLIAESDLNDARLVTAREGGGYGLHAQWADDLHHALHVALSGETFGYYPDFEGKLATTLERVFLHDGTWSSFRGRAHGRPVDRERLPGYRFLAYLQNHDQIGNRATGDRLTATVSPERLAIGAAIVLCSPYTPMLFMGEEWGARTPWRFFASFPDPQLAEAVRTGRRREFARHGWGESDVPDPVDPATVEASKLDWAEVSRPEHARVLELHRALIRLRREHPELADPRLDRFRVEQRGSVLVLHRGDLRLLCNLAPAGGVPSGEGAVGGAAGAAVGAGAAGGADGALARPGGSRPGAADAGAPGPGARDAEVDLGVAPVAVLLASGEAEVAGQVLSLPAETFAVVQLPGSQPTSVSRSARS
>NZ_CP023445.1|WP_015803820.1|5997356_5997848_+|ANTAR-domain-containing-protein
MVGDMGQDDSLTARIASLEAEVRGLRNAVQTRTVIGQATGLIAAVQGCTPQQGFQLLVRMSQHHNVKLHTIAVKLIDLAAELGPHRAVRAVQVSEEQNGVPTPVDWPGADVVQAARQLVAAYDAATASSGHEPEARRQLTDQVNLAGQLLAERLTEVGWLPGS
>NZ_CP023445.1|WP_084799265.1|5996897_5997065_-|CsbD-family-protein
MDDKASNKAEELKGRAKEGVGEATGNEQWQAEGRAERASGALKQGIEKVKDAFRK
>NZ_CP023445.1|WP_096497997.1|6009942_6010701_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MRGRVTAAAVVAGAIATGSGFFNAVGTSAIPLAAGGDLAGALLVPSEGAPAQASGALLTVHEVNPGLESAKLVRGEGMVALQQVDRVVQQASADYAVKQEELRKQQEAEAAEKARREAEEAAKRPKVVKPAQGSFTSGFGARWGTTHYGIDIANSIGTPILSAMDGTVIEAGSASGFGLWVRVQHDDGTVTVYGHVDTIVAYAGTRVSAGQQIATMGNRGQSTGPHLHFEVWLNGGQKIDPVGWLAQRGIAL
>NZ_CP023445.1|WP_096496025.1|6011400_6013482_-|penicillin-binding-protein
MVGLCLTAGVLVAAVLFPVVGGLGLASNRAADTVDQTSGELTKAELPLVTTIQDKDGQPIAYLYDQYRIPVAFEDIADTMKAAIIAIEDRRFFEHQGVDWQGIMRAAAKAGVEGETSQGASTLTQQYVKNYLAFVVGKGSDEAYEKATAATMARKLSEARIAMQLEQKMTKEEILTAYLNVVPFGNGTYGVGAAAQTYFNTTADKLTVPQAALLAGLVNRPSALNPEAGADAAMERRNTVIDYMRNNGAFGEDTARADQLTEEYKAAPIGVVEDLKLLPMGCVGAGDGPIYGSFCRYLIDYLLEHGLTEDDLRRGGLTIKSTMDAKATQAVKEAAEGQVSKTTPGVANAMAVVEPGKDKHRVRALAANRDFGNNADAGQSAYSLPAEVTRFGAGSIYKVFTAAAAMEQGKTGIDRQVPVPNTYTSRVYRDGNKGYTVKNYSDGADTSMTLTKALATSPNTGFIILEEQAGLNNVVDMAYRLGLRDGMQGVTLAGDPLKEDKSNGPSQGDAVKQGNMGSFTLGAGPTSVLELANVSATIVSEGTWCPPTPIEQVLDRNGNPVQLQEAACEQAVSPELAAALAQGMSHDTTAGGTAAGAASRAGWNRPTIGKTGTTENYWSVGFMGATMQYAGAVLTFTDGASPQVLCGNPVRLCGQGRTGLTGGEVAAPTWFNAMNKIHEGLPAVPLPPATKYR
>NZ_CP023445.1|WP_096496026.1|6013824_6014868_-|carbohydrate-kinase-family-protein
MRMSDEAPSFDVLLSGTVFLDIIFTGLPRPPAPGTEVWADGLGSCPGGIANLAVALRRLELRTGLSAAFGEDVYADFCWEVLAEQEKVDLGHCRRFYGWHTPVTVSMAMDHDRSMVTHGHQPPVTADELLDPPPSTRACFVHLQAEDEAWVRKAKEGGALLFADIGWDRTEAWAPDLLTRLDGYDAFLPNSVEAMSYTRSSTPELAAERLAELVPVVVVTRGGGGAVAVDSATGERADVPGLSVAALDPTGAGDVFGAGFVLGTLEGWPLAQRVRFANLCAALSTQHFGGSLSAPGWADIAMWWRTVRRRARDERELREYGFLEDVLPQHGGDEVRRASATIRLAPK
>NZ_CP023445.1|WP_015803832.1|6014880_6015612_-|sigma-70-family-RNA-polymerase-sigma-factor
MGHHAVVRADFEIEGIEAVGGDGAVAGEGRRIRLVGSGPEPEPGGPSAAWLAEAELGDLVDHALAGRPRAVDQLLTRVQPLVLRYCRARVGMRERTLVSAEDIAQEVCLAVVAALGRYRYEPTSFLAFVYGIAAHKVADARRRAVRSRSEVVPELPDTPALEDGPEQRAVNGELIGHITRMLGKLPARQREILVLRVAVGLTAEETAAAVGSTPGAVRVAQHRALTRMREMAAAVDRVDRSAS
>NZ_CP023445.1|WP_096497998.1|6016052_6016871_+|alpha/beta-hydrolase
MSVRTDQGVFDAIAAGPEDGRPVLLLHGFPQAALCWEHQVAVLGREGYRAVAFDQRGYSPGARPAEVSAYGTGSLVGDVLAVADELGWPVFDLVGHDWGGAVAWWAAAEHPERLRSLTVVSTPHPAALGEAMRTDEEQHQRSGYMAQLRASGAEKQLLANDAEALRRIFDWRVQPGRVDEYVSRLKEPGALTAALNWYRASRPDGRIGKVTVPTLYVWTTEDVAFGSTAALATGDWVTGPYTFRMLEDVSHWAPEEAPEAVTALLLANLSIS
>NZ_CP023445.1|WP_041837014.1|6016922_6017108_+|helix-turn-helix-transcriptional-regulator
MTELTYSERRVATLAACGHSNRAIAMRLHITVSTVEQHLTRVYRKLSVASRTELKGHSALV
>NZ_CP023445.1|WP_096496027.1|6017112_6017667_+|nucleotidyltransferase-family-protein
MGVTGLLLAAGAGRRYGRPKALVSQGGALWVETACGVLRAAGCDRVVVVLGASSARVRATASLGDAVVVDNADWSTGVGSSLRVGLAAAGDRDAVAVLPVDTPGVTADAVARLLVLASPAVLARACYAGVPGHPVLIGRDHWGPVSESAHADVGARDYLVEHGVLMVPCEDVADGDDVDAPPAT
>NZ_CP023445.1|WP_096496028.1|6017659_6018556_-|LysR-family-transcriptional-regulator
MDLETRELRYFVTVAEELHFGRAAERLGMAQPPLSRAIQRLERRLGAVLLERDRRGVALTPAGEVLLREGRVVLDAATAAANRVRRAGGRIVLAVKAGADHELLSRVLPAYREEVGAGEVEVLLCGIGEQAGLLRAGRADAALVHRPFDDVAGFDTEELLVEEQVAVLPARHPLARRESLTMSEIADVPGLPLARWPRLEGGYPPGPGPEVRDQAQVSQLIALGLALLVIPASSRAWQWAEHAGVPVVDAPPVTTLIAWQPHSRSPALAGLVRAAVRVGEEMGFGSRGRPAVVAGSIK
>NZ_CP023445.1|WP_096496029.1|6018652_6019393_+|SDR-family-oxidoreductase
MNEQKKTALVTGANKGIGYAIAAGLGALGHRVGVGARDDARREEAVARLRAAGVDAFGVPLDVTDDTSAATAARLLEGSGHGLDVLVNNAGISGAHAPDWSQDPTTLDLAEARRVVETNVFGVIRVTNALLPLLRESPAPRIVNLSSSVASLTRQADPDAQSGPIMAVYAPTKSYLNAVTVQYARQLAGTGVLVNAACPGLVATDFTGFQAPRTPEQGAATAIRLATLPGGGPSGGFYDDEGPLPW
>NZ_CP023445.1|WP_096497999.1|6019430_6020195_-|DeoR/GlpR-transcriptional-regulator
MNSVDVAQRHEVILGSLRHGGRVGVAEIAELVGCSEMTVRRDLDVLEREGLLRRVRGAAVGMLTGQATPYSARVRQRVEAKRRIGAAVAAMLDDGETAVLDAGTTTLEVARSLVDRRVTVLALSLHAVDLLRGSAQVRLLLPGGEVRAGEQAFTGPLTEHAFRVMRFDTVVLSSCGLSARDGVSAHDLGESAVKLAAVGAAGRVVAAVDSSKFGRTAFGRVCGVEEIDVLVTDVDAPADEVARIRDAGVEVVLV

Crispr_ID: NZ_CP023445_11

• CRISPR_ID: NZ_CP023445_11
• CRISPR_location: 6861456-6861566
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_11

Consensus_repeat	Method
CGCTGTCCCAGCCGCACCGATCCCCG	CRISPRCasFinder

spacers of NZ_CP023445_11

>11.1|6861482|59|NZ_CP023445|CRISPRCasFinder
ACCCGGCCCGACCCGGTCATCCACCAGCCGCTTCGGCCGCCACACCAGCGACCCACCCG

CRISPR arrays and Neighbor proteins around NZ_CP023445_11

CRISPR arrays

The CRISPR arrays of NZ_CP023445_11

>merge|NZ_CP023445|11|6861456-6861566|CRISPRCasFinder
CGCTGTCCCAGCCGCACCGATCCCCGACCCGGCCCGACCCGGTCATCCACCAGCCGCTTCGGCCGCCACACCAGCGACCCACCCGCCGCTGTCCAGCCGCACCGATCCCCG

>NZ_CP023445|11|10|6861456-6861566|CRISPRCasFinder
CGCTGTCCCAGCCGCACCGATCCCCG	ACCCGGCCCGACCCGGTCATCCACCAGCCGCTTCGGCCGCCACACCAGCGACCCACCCG
CCGCTGTCCAGCCGCACCGATCCCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_015804654.1|6864254_6864683_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP023445.1|WP_096496615.1|6852149_6852782_+|hypothetical-protein	unknown	unknown	gnl|CDD|274422
NZ_CP023445.1|WP_096496618.1|6858516_6859005_-|RNA-polymerase-subunit-sigma-24	unknown	unknown	gnl|CDD|236605
NZ_CP023445.1|WP_157767894.1|6860046_6860616_+|hypothetical-protein	unknown	unknown	gnl|CDD|223021
NZ_CP023445.1|WP_041837118.1|6852828_6853155_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496620.1|6859324_6860032_+|CAP-domain-containing-protein	unknown	unknown	gnl|CDD|349398
NZ_CP023445.1|WP_096496629.1|6867881_6868598_-|DivIVA-domain-containing-protein	unknown	unknown	gnl|CDD|226127
NZ_CP023445.1|WP_015804658.1|6866990_6867173_-|50S-ribosomal-protein-L32	unknown	unknown	gnl|CDD|237038
NZ_CP023445.1|WP_096496628.1|6867175_6867763_-|metal-binding-protein	unknown	unknown	gnl|CDD|224317
NZ_CP023445.1|WP_096496626.1|6865900_6866152_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_015804661.1|6868734_6869217_-|pantetheine-phosphate-adenylyltransferase	unknown	unknown	gnl|CDD|234674
NZ_CP023445.1|WP_096496625.1|6865015_6865891_-|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	unknown	unknown	gnl|CDD|234899
NZ_CP023445.1|WP_096496617.1|6857695_6858517_-|zf-HC2-domain-containing-protein	unknown	unknown	gnl|CDD|379219
NZ_CP023445.1|WP_096496624.1|6863254_6863935_-|response-regulator	unknown	unknown	gnl|CDD|182522
NZ_CP023445.1|WP_096496627.1|6866186_6866963_-|ribonuclease-III	unknown	unknown	gnl|CDD|234633
NZ_CP023445.1|WP_096496619.1|6859038_6859326_-|acylphosphatase	unknown	unknown	gnl|CDD|237712
NZ_CP023445.1|WP_096496622.1|6860773_6861265_+|hypothetical-protein	unknown	unknown	gnl|CDD|235906
NZ_CP023445.1|WP_096498062.1|6854070_6857646_-|chromosome-segregation-protein-SMC	unknown	unknown	gnl|CDD|274008
NZ_CP023445.1|WP_096496616.1|6853245_6854031_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_CP023445.1|WP_096496623.1|6862029_6863151_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224172

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_015804654.1|6864254_6864683_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	2.95017e-17
NZ_CP023445.1|WP_096496615.1|6852149_6852782_+|hypothetical-protein	gnl|CDD|274422	TIGR03083, TIGR03083, uncharacterized Actinobacterial protein TIGR03083. This protein family pulls together several groups of proteins, each very different from the others. They share in common three conserved regions. The first is a region of about 38 amino acids, nearly always at the N-terminus of a protein. This region has a bulky hydrophobic residue, usually Trp, at position 29, and a His residue at position 37 that is invariant, so far, in over 150 instances. The second conserved region has a motif [DE]xxxHxxD. The third conserved region contains a hydrophobic patch and a well-conserved Arg residue. Most examples are found in the Actinobacteria, including the genera Mycobacterium, Corynebacterium, Streptomyces, Nocardia, Frankia, etc. The pattern of near-invariant residues against a backdrop of extreme sequence divergence suggests enzymatic activity and conservation of active site residues.	1.25919e-05
NZ_CP023445.1|WP_096496618.1|6858516_6859005_-|RNA-polymerase-subunit-sigma-24	gnl|CDD|236605	PRK09645, PRK09645, ECF RNA polymerase sigma factor SigL.	8.81569e-38
NZ_CP023445.1|WP_157767894.1|6860046_6860616_+|hypothetical-protein	gnl|CDD|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	0.000788516
NZ_CP023445.1|WP_096496620.1|6859324_6860032_+|CAP-domain-containing-protein	gnl|CDD|349398	cd05379, CAP_bacterial, Bacterial CAP (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) domain proteins. Little is known about bacterial and archaeal members of the CAP (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) domain family. The wider family of CAP domain containing proteins includes plant pathogenesis-related protein 1 (PR-1), cysteine-rich secretory proteins (CRISPs), and allergen 5 from vespid venom, among others. Studies of eukaryotic proteins show that CAP domains have several functions, including the binding of cholesterol, lipids and heparan sulfate. This group includes Borrelia burgdorferi outer surface protein BB0689, which does not bind to cholesterol, lipids, or heparan sulfate, and whose function is unknown.	1.4056e-40
NZ_CP023445.1|WP_096496629.1|6867881_6868598_-|DivIVA-domain-containing-protein	gnl|CDD|226127	COG3599, DivIVA, Cell division initiation protein [Cell division and chromosome partitioning].	5.8986e-26
NZ_CP023445.1|WP_015804658.1|6866990_6867173_-|50S-ribosomal-protein-L32	gnl|CDD|237038	PRK12286, rpmF, 50S ribosomal protein L32; Reviewed.	1.23085e-22
NZ_CP023445.1|WP_096496628.1|6867175_6867763_-|metal-binding-protein	gnl|CDD|224317	COG1399, COG1399, Predicted metal-binding, possibly nucleic acid-binding protein [General function prediction only].	1.51789e-30
NZ_CP023445.1|WP_015804661.1|6868734_6869217_-|pantetheine-phosphate-adenylyltransferase	gnl|CDD|234674	PRK00168, coaD, phosphopantetheine adenylyltransferase; Provisional.	2.83313e-97
NZ_CP023445.1|WP_096496625.1|6865015_6865891_-|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	gnl|CDD|234899	PRK01103, PRK01103, bifunctional DNA-formamidopyrimidine glycosylase/DNA-(apurinic or apyrimidinic site) lyase.	2.62992e-144
NZ_CP023445.1|WP_096496617.1|6857695_6858517_-|zf-HC2-domain-containing-protein	gnl|CDD|379219	pfam13490, zf-HC2, Putative zinc-finger. This is a putative zinc-finger found in some anti-sigma factor proteins.	7.34758e-05
NZ_CP023445.1|WP_096496624.1|6863254_6863935_-|response-regulator	gnl|CDD|182522	PRK10529, PRK10529, DNA-binding transcriptional activator KdpE; Provisional.	5.19373e-90
NZ_CP023445.1|WP_096496627.1|6866186_6866963_-|ribonuclease-III	gnl|CDD|234633	PRK00102, rnc, ribonuclease III; Reviewed.	3.2426e-115
NZ_CP023445.1|WP_096496619.1|6859038_6859326_-|acylphosphatase	gnl|CDD|237712	PRK14422, PRK14422, acylphosphatase; Provisional.	6.95989e-44
NZ_CP023445.1|WP_096496622.1|6860773_6861265_+|hypothetical-protein	gnl|CDD|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	0.00129076
NZ_CP023445.1|WP_096498062.1|6854070_6857646_-|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_CP023445.1|WP_096496616.1|6853245_6854031_+|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.	1.41961e-49
NZ_CP023445.1|WP_096496623.1|6862029_6863151_+|FAD-dependent-oxidoreductase	gnl|CDD|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	3.47706e-70

Protein sequences

>NZ_CP023445.1|WP_096496622.1|6860773_6861265_+|hypothetical-protein
MFEQESVVAARRRFSPLVLLSAAGAVVAAAVAGVGAALVPDGEPETPRPLEAQAEATTGSAPARPTSESTAAAPTQLRAAATTTTTRRPDARHEDRPTRGDEPTAARSESPEEPDEPVALPTTTTRQSPTTTTTAPPVVTTTPEDEAPDPTTTAPTTTRPPRP
>NZ_CP023445.1|WP_157767894.1|6860046_6860616_+|hypothetical-protein
MTDDGLYESPEPEQSSRARRLSPHLLLAASGVVVATIFGAVAAIAGPSSSDEATTPIGVQLDTPPTGRTSTPTSAPESGSESAGSSSEAPSSTPQSAESSAAPTTTTQRVRVTTVTRADGTTTTTTVNEEPQPPKPNNPNPNPNPNPNPNPNPGGTTTTTKPPVEPPVTTTSAEQPPTSGSGTPPTSGN
>NZ_CP023445.1|WP_096496620.1|6859324_6860032_+|CAP-domain-containing-protein
MPSTPVFHPMVIRCATVSARSGKRSAIGGLLGLLLGAAGVGSIALLVGLTASTTSQQDPPPGAPRSGPGPGPGSSGAPDGPRSTTATTSGLAPDSPAPASSSPTSPQDPPPLDVVQADRVVRLVNQARGAAGCAALGVDDRVVTAARAHSADMASRGYFAHTSPEGVDFATRMREAGYPRPAGENIAMGQRSAEDVVGAWLDSEGHRRNILDCSFTTTGVGLDTRGWYWTQNFGR
>NZ_CP023445.1|WP_096496619.1|6859038_6859326_-|acylphosphatase
MSGAESAVRMTAWVRGHVQGVGFRWWTRARALELGLVGSASNLRDGRVEVNAEGPEEACRALLAALRSGGAPGRVDVVVERWSSPRGGLTGFAER
>NZ_CP023445.1|WP_096496618.1|6858516_6859005_-|RNA-polymerase-subunit-sigma-24
MDRGEDVVRQLYGRWRGPLRGYVLRLVGGDHRYAEDVVQETLRRARGSADVRTPEEAGPWLYAVARALVASGFRRAGGERPEEPPSEVDAVDHALQGWQVAEALRGLSRDHRDAVVELHYRRRTVAEAAAALGIPQGAVKSRCFYGLRALRDALAERGVTEP
>NZ_CP023445.1|WP_096496617.1|6857695_6858517_-|zf-HC2-domain-containing-protein
MTCFRSTDLGVYLLGSLDPVERGAFERHLRACPPCRRELLRLAPLPGLLGQVTLLDLEQPFTDPDPSPELAPLPELPPQPPPAVPRSARISARTTLPLATPLPPAPDGWLVGSRATRAGRGDRARDAGRTAGRRGPRWPLVAAAAALFGVLLVGALLVTPGWFAREDRGPVPVASSTAVTWAGTDAGTGVAARAELVGRDWGTELLLTLDGAPDGARCRLVVHGTSGRTEVAGWWGSGPARHERVPGATSFALADVERVDVVADMRVLVSVRP
>NZ_CP023445.1|WP_096498062.1|6854070_6857646_-|chromosome-segregation-protein-SMC
MHLKSLTLKGFKSFASATTLRFEPGITCVVGPNGSGKSNVLDALRWVMGTQGAKDLRGGKMEDVIFAGTSGRAPLGRAEVTLTIDNADGALPIEYTEVSITRRMFREGATEYEINGSSCRLMDIQELLSDSGIGREMHVIVGQGQLSAILESKPEERRAFIEEAAGVLKHRKRKEKALRKLEAMQANLTRLTDLTAELRRQLKPLGKQAEIARRAQTVQAELRDSRMRLLADDLVTQRESLARDEQDEAAARARRAEVERSLQQAQVQQNELEEVVSADAPKLQQAQDTWYRLSALEERLRGTVRLAVERERHLKASVDAPRGGRDPEELEAEAEQTAALELELQEGVTEARVGLAEAVETRAELERMVSAAEKAHLAAVRAIADRREGLARLSGQVEALRSKTNATAEEIERLSVALTEAVERSEVAQEELAEARESTDSEDEDDAGVQERHRHAVEAEDAARRRVEELVKAERAAERDIASWKARVDALSLGLTRKDGAGALLASQLPGLLGSVAALLTVEPGNEVALAAALGPVADAIAVASGDDALAALELLKSEDAGRAGVVIGGGEPPTGALPALPGGARWAVDLVRAPEALRPAVARALHGLAVVADLAAADALVRAHPELRAATGEGDLLGSDWATGGSGRSQSVIEVQAAVDEASEKLALAERALEHSGPALDGARAEQQARRGEASALKEQLNEAKVRRARSSERLNRLAAAVRSAEAEVERARGQREKVEAAREENLLKLAELEERLLVAEEQPLDDEPDTAQRDEAAAELASARQGEMDARLALRTAEERARALQGKAEGLRRAARAERETRERAQRALAARARGAVVASAVVRGGEVALERIAVSLDRAARERDAAQERRARHEALLGQVRGLVREMSGELEKLTDAVHRDEVLRAEQRLRIEQLEVKISEDFGIGLDDLVAEYGPDVHVPPSAGELAEYEAAKERGEAVTAPLPIPYDRDTQARRAKRAERDLSLLGKVNPLALEEFAALEERYKFLSNQLEDIKATRRDLLTVVKEVDDKILEVFTLAYEDVAREFQVVFEVLFPGGEGRLVLTEPDDMLTTGIELEARPPGKKVKRLSLLSGGEKSLAAVAMLVAIFRARPSPFYVMDEVEAALDDTNLHRLIGLFEQLRERSQLLIITHQKPTMEIADALYGVSMRGDGISQVISQRLRGREAS
>NZ_CP023445.1|WP_096496616.1|6853245_6854031_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MADLVYPPVIALAKTLFRALDLRIDIRGAEHVPTTGGAVLAVNHISYLDFILAGYGAHPAKRLVRFMAKEEIFRNKIAGPLMRGMKHISVDRSAGKESYEKALAALRSGEVVGIFPEGTTGRSYVVNTVKSGAIRLARAAGVPLIPMALWGTQRLLGKGTPRNLTQRHVPITIEIGAPFEPADETELRARMQELLDKAQREYPDDGVGQWWHPANLGGTAPTPEEVAVLEAKAREAREKRAQEKRDQEKRDQEKRAQEKRG
>NZ_CP023445.1|WP_041837118.1|6852828_6853155_+|hypothetical-protein
MSEETIHLELNDNGVAVDLPVPSNGRDQVQEVPYRPVEFRDNDLPSALERAATWLRQTQEWLGEAVDVISVHLDYDDTKGSPYFNLKLLCNEEDLAGVPKVRREHGER
>NZ_CP023445.1|WP_096496615.1|6852149_6852782_+|hypothetical-protein
MAGGAGGGAVDDGAGGPGGALTGADVRSAAGECAAFLAGFADRDWAVPVPGLDWTVARTAAHLVDCLRWYALDLAGGTEELDCWLEATDATADPAMLVRVVRAQSEVLAATIDAAPPGHRGWHPSGLPEPAGFAAMACDELLVHTWDAGRGFGAEFTPTGRQAAATLARLFPAHEPGADAWRALLWANGRVELPGRPSQSGWKWHGDPLT
>NZ_CP023445.1|WP_096496623.1|6862029_6863151_+|FAD-dependent-oxidoreductase
MSERVVVLGAGYAGLAAAKLAARWTGARVTLVNERDRFVQRVRLHQLAAGRPERRLPLRDLLAGAGVELVVGRAEAIDLGAREVRVGDRALPYDRLVYALGSGADLGSTPGVAEHAHSVADAESAERLHRALSGGGSGARGGRRSVVVVGGGLTGVETAAELAEAGHSVALLSSGAVGAGLSPKAVRHLHRAFARLGVRVREGCRVESVDARGVRVDGVREAADAVVWTAGFRVPPLARESGLAVDASGRLLVDGAMRSTSHPEVIGVGDAAAMRRADGQEMRMACATAGPNAQRAIRALAQELAGAEPTPTRFRYVGQCVSLGRRDAVLQFTHPDDTPRDLVLTGRAAALAKEAIIAYTVAFQRRPTLPSGA
>NZ_CP023445.1|WP_096496624.1|6863254_6863935_-|response-regulator
MTKVLVVDDEPQIVRALRINLSARGYQVLTAHDGAAALRAAAEGKPDVVVLDLGLPDVDGTEVIAGLRGWTTVPIIVLSARVDSTDKVEALDAGADDYVTKPFGMDELLARLRAAVRRSAAPADAGEAVVRTGAFTVDLVAKKVHREGAEVHLTPTEWGLLEVLVRNPGKLVAQRQLLQEVWGPAYAKETHYLRVYLAQLRRKLEPEPSRPRHLVTEPGMGYRFEP
>NZ_CP023445.1|WP_015804654.1|6864254_6864683_+|MarR-family-transcriptional-regulator
MTASVTNQDALQLVVAVHRLVRSLRQSASVRRLQPTQLLVLAELSNHGPMRIGEIAVRALCSQPTATTVVTGLESNGLVRREADPADGRATIVVLTGAGRETVLSMAHGEAELLSERLSALSPEEQHRVRAVTPLLRRLADR
>NZ_CP023445.1|WP_096496625.1|6865015_6865891_-|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase
MPELPEVEVVRRGLHEHVTGRTVASVEVLHARAIRRHLPGAADFAVRLTGQRMDAARRRGKYLWVDLSGGEAVLAHLGMSGQMLVQPVGAPDEKHLRVRVVFEDDGPELRFVDQRTFGGLALDELVEVDGTWLPRQVSHIARDPMDPEFDADAAVRALRSRKTDVKRALLDQTLVSGVGNIYADESLWRARLHGLRPTAKLTTAKTAELLGHATQVMLEALGQGGTSFDALYVNVNGQSGYFDRSLAVYGQEDRPCARCGTAIVREPFMNRSSYSCPRCQPRPRDAKTAAR
>NZ_CP023445.1|WP_096496626.1|6865900_6866152_-|hypothetical-protein
MYATNVRSRRAHHRGHTSRPLSAARSGGIQGLVLVRDTAQAGGWMLKPTKPQAAAFELLEELEREVAARAETAEHAAAGTTED
>NZ_CP023445.1|WP_096496627.1|6866186_6866963_-|ribonuclease-III
MGGRSSRGRSVDRTPLLEALGVPLDAELLTLALTHRSYAYENGGLPPNERLEFLGDAVLGLVVTDHLYRAHPDRPEGQLAKLRASVVNMHALAGVARGLGADGLGGHLLLGRGEELTGGRDKASILADGLEAVIGAVYLQFGIDTARQLVHHLFDPLLAEAPLRGAGLDWKTSLQELTASSGLGVPEYRVDDQGPDHRKEFTATVYVGGKPHGSGDGRTKKEAEQKAAEAAWRVLSDKADDGEDAADGAEQNGQGSAN
>NZ_CP023445.1|WP_015804658.1|6866990_6867173_-|50S-ribosomal-protein-L32
MAVPKRKMSRSNTRSRRAQWKTAAVHLVACSNKACRQPKPQHVACPTCGQYDGRQVVQPA
>NZ_CP023445.1|WP_096496628.1|6867175_6867763_-|metal-binding-protein
MPEHSRAHARSTAPGPWVIDTRDLGRRAGSSRAYRRTVPAEGLGLLGVIAVPEGGEVELDLLLESVVEGVLVTGTASTTVEGECSRCLDPLSSDVQVGLTELYAYPDSTTDETTEEDEVSRVHDDLIDLEPVVRDALVLALPQVPLCSPDCLGLCVDCGGRLADLGPDHGHETIDPRWAALQARFDGNRDNPEEN
>NZ_CP023445.1|WP_096496629.1|6867881_6868598_-|DivIVA-domain-containing-protein
MYRVFEALDELVTIVEEARGVPMTSGCVVPRGDVLELLDDVRDAIPAELDDAQDVLDHRDELVGKAQHEADQATSKARSEADRMLAEAQHEAERMLSEASARAERLVAEAEEQAERAVAAGRQEYEDLVGRAHSEADRMVQAGRANYERAIEEGRAEQARLVDQTEVVQAAHVESARVMEAAQAEAMRLRGECDAYVDGKLADFEDLLAHTLRSVGKGRSHLRGPAVASATAPYDYQD
>NZ_CP023445.1|WP_015804661.1|6868734_6869217_-|pantetheine-phosphate-adenylyltransferase
MTRAVCPGSYDPATNGHLDIIGRAAGLFDEVVVSVLINKSKKTLFSVEERTEMLREVTAQWPNVRVDSWHGLLVDYCRENDIQAIVKGLRAVSDYDYELQMAQMNHQLTGVETLFMPTNPIYSFLASSLVKDVANYGGDVSTLLPPSILTRLTQRLAERR

Crispr_ID: NZ_CP023445_12

• CRISPR_ID: NZ_CP023445_12
• CRISPR_location: 6921322-6921439
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_12

Consensus_repeat	Method
CGGCGCGACGGTGGGCGGGCCGTTTTTCC	CRISPRCasFinder

spacers of NZ_CP023445_12

>12.1|6921351|60|NZ_CP023445|CRISPRCasFinder
CGACGCCCCGGCCGCGCGGCGCGGCGACGGGCAGGCCGTTTTCCCGGCGCTCCTACCGCA

CRISPR arrays and Neighbor proteins around NZ_CP023445_12

CRISPR arrays

The CRISPR arrays of NZ_CP023445_12

>merge|NZ_CP023445|12|6921322-6921439|CRISPRCasFinder
CGGCGCGACGGTGGGCGGGCCGTTTTTCCCGACGCCCCGGCCGCGCGGCGCGGCGACGGGCAGGCCGTTTTCCCGGCGCTCCTACCGCACGGCGCGACGGTGGACGGGCCGTTTTTCC

>NZ_CP023445|12|11|6921322-6921439|CRISPRCasFinder
CGGCGCGACGGTGGGCGGGCCGTTTTTCC	CGACGCCCCGGCCGCGCGGCGCGGCGACGGGCAGGCCGTTTTCCCGGCGCTCCTACCGCA
CGGCGCGACGGTGGACGGGCCGTTTTTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096496667.1|6910921_6912325_-|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl|CDD|235490
NZ_CP023445.1|WP_096496677.1|6930752_6932588_-|acetolactate-synthase-large-subunit	unknown	unknown	gnl|CDD|236098
NZ_CP023445.1|WP_096496674.1|6922998_6926277_-|S8-family-serine-peptidase	unknown	unknown	gnl|CDD|173800
NZ_CP023445.1|WP_096496669.1|6914762_6916253_-|glutamate--tRNA-ligase	unknown	unknown	gnl|CDD|234953
NZ_CP023445.1|WP_096496671.1|6918626_6919280_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096498066.1|6917799_6918570_-|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_CP023445.1|WP_041838493.1|6912442_6913105_+|IclR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224332
NZ_CP023445.1|WP_157767898.1|6932879_6933476_+|PH-domain-containing-protein	unknown	unknown	gnl|CDD|371225
NZ_CP023445.1|WP_096496665.1|6909224_6910097_-|HU-family-DNA-binding-protein	unknown	unknown	gnl|CDD|259858
NZ_CP023445.1|WP_096496673.1|6921678_6922716_-|3-isopropylmalate-dehydrogenase	unknown	unknown	gnl|CDD|179579
NZ_CP023445.1|WP_096496666.1|6910304_6910907_-|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl|CDD|179314
NZ_CP023445.1|WP_096496670.1|6916341_6917574_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|235729
NZ_CP023445.1|WP_096496680.1|6934147_6935992_+|dihydroxy-acid-dehydratase	unknown	unknown	gnl|CDD|237104
NZ_CP023445.1|WP_096496679.1|6933611_6934031_+|vitamin-K-epoxide-reductase-family-protein	unknown	unknown	gnl|CDD|240601
NZ_CP023445.1|WP_096496668.1|6913920_6914604_-|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223943
NZ_CP023445.1|WP_096496676.1|6928744_6929014_-|DUF397-domain-containing-protein	unknown	unknown	gnl|CDD|377231
NZ_CP023445.1|WP_096496675.1|6926713_6928312_-|phosphoglycerate-dehydrogenase	unknown	unknown	gnl|CDD|237436
NZ_CP023445.1|WP_096496672.1|6919325_6920939_-|citramalate-synthase	unknown	unknown	gnl|CDD|237068
NZ_CP023445.1|WP_015804712.1|6930197_6930704_-|acetolactate-synthase-small-subunit	unknown	unknown	gnl|CDD|183365
NZ_CP023445.1|WP_015804711.1|6929126_6930140_-|ketol-acid-reductoisomerase	unknown	unknown	gnl|CDD|235491

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096496667.1|6910921_6912325_-|3-isopropylmalate-dehydratase-large-subunit	gnl|CDD|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_CP023445.1|WP_096496677.1|6930752_6932588_-|acetolactate-synthase-large-subunit	gnl|CDD|236098	PRK07789, PRK07789, acetolactate synthase 1 catalytic subunit; Validated.	0
NZ_CP023445.1|WP_096496674.1|6922998_6926277_-|S8-family-serine-peptidase	gnl|CDD|173800	cd07474, Peptidases_S8_subtilisin_Vpr-like, Peptidase S8 family domain in Vpr-like proteins. The maturation of the peptide antibiotic (lantibiotic) subtilin in Bacillus subtilis ATCC 6633 includes posttranslational modifications of the propeptide and proteolytic cleavage of the leader peptide. Vpr was identified as one of the proteases, along with WprA, that are capable of processing subtilin. Asp, Ser, His triadPeptidases S8 or Subtilases are a serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	2.09083e-51
NZ_CP023445.1|WP_096496669.1|6914762_6916253_-|glutamate--tRNA-ligase	gnl|CDD|234953	PRK01406, gltX, glutamyl-tRNA synthetase; Reviewed.	0
NZ_CP023445.1|WP_096498066.1|6917799_6918570_-|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	2.67042e-98
NZ_CP023445.1|WP_041838493.1|6912442_6913105_+|IclR-family-transcriptional-regulator	gnl|CDD|224332	COG1414, IclR, Transcriptional regulator [Transcription].	9.57055e-52
NZ_CP023445.1|WP_157767898.1|6932879_6933476_+|PH-domain-containing-protein	gnl|CDD|371225	pfam10756, bPH_6, Bacterial PH domain. This domain has a bacterial type PH domain structure. This domain was previously known as DUF2581. This family is conserved in the Actinomycetales. Although several members are annotated as RbiX homologs, RbiX being a putative regulator of riboflavin biosynthesis, the function could not be confirmed.	1.34549e-07
NZ_CP023445.1|WP_096496665.1|6909224_6910097_-|HU-family-DNA-binding-protein	gnl|CDD|259858	cd13836, IHF_B, Beta subunit of integration host factor (IHFB). This subfamily consists of the beta subunit of integration host factor (IHF) and IHF-like domains. IHF is a nucleoid-associated protein (NAP) that binds and sharply bends many DNA targets in a sequence specific manner. It is a heterodimeric protein composed of two highly homologous subunits IHFA (IHF-alpha) and IHFB (IHF-beta). It is known to act as a transcription factor at many gene regulatory regions in E. coli. IHF is an essential cofactor in phage lambda site-specific recombination, having an architectural role during assembly of specialized nucleoprotein structures (snups). IHF is also involved in formation as well as maintenance of bacterial biofilms since it is found in complex with extracellular DNA (eDNA) within the extracellular polymeric substances (EPS) matrix of many biofilms.	6.87822e-27
NZ_CP023445.1|WP_096496673.1|6921678_6922716_-|3-isopropylmalate-dehydrogenase	gnl|CDD|179579	PRK03437, PRK03437, 3-isopropylmalate dehydrogenase; Provisional.	0
NZ_CP023445.1|WP_096496666.1|6910304_6910907_-|3-isopropylmalate-dehydratase-small-subunit	gnl|CDD|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	8.47203e-121
NZ_CP023445.1|WP_096496670.1|6916341_6917574_+|FAD-dependent-oxidoreductase	gnl|CDD|235729	PRK06185, PRK06185, FAD-dependent oxidoreductase.	0
NZ_CP023445.1|WP_096496680.1|6934147_6935992_+|dihydroxy-acid-dehydratase	gnl|CDD|237104	PRK12448, PRK12448, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP023445.1|WP_096496679.1|6933611_6934031_+|vitamin-K-epoxide-reductase-family-protein	gnl|CDD|240601	cd12918, VKOR_arc, Vitamin K epoxide reductase family in archaea and some bacteria. This family includes vitamin K epoxide reductase (VKOR) mostly present in archaea and some bacteria. VKOR (also named VKORC1) is an integral membrane protein that catalyzes the reduction of vitamin K 2,3-epoxide and vitamin K to vitamin K hydroquinone, an essential co-factor subsequently used in the gamma-carboxylation of glutamic acid residues in blood coagulation enzymes. All homologs of VKOR contain an active site CXXC motif, which is switched between reduced and disulfide-bonded states during the reaction cycle. In some bacterial homologs, the VKOR domain is fused with domains of the thioredoxin family of oxidoreductases which may function as redox partners in initiating the reduction cascade.	6.52683e-36
NZ_CP023445.1|WP_096496668.1|6913920_6914604_-|HAD-family-hydrolase	gnl|CDD|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	5.1435e-37
NZ_CP023445.1|WP_096496676.1|6928744_6929014_-|DUF397-domain-containing-protein	gnl|CDD|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	4.9512e-13
NZ_CP023445.1|WP_096496675.1|6926713_6928312_-|phosphoglycerate-dehydrogenase	gnl|CDD|237436	PRK13581, PRK13581, D-3-phosphoglycerate dehydrogenase; Provisional.	0
NZ_CP023445.1|WP_096496672.1|6919325_6920939_-|citramalate-synthase	gnl|CDD|237068	PRK12344, PRK12344, putative alpha-isopropylmalate/homocitrate synthase family transferase; Provisional.	0
NZ_CP023445.1|WP_015804712.1|6930197_6930704_-|acetolactate-synthase-small-subunit	gnl|CDD|183365	PRK11895, ilvH, acetolactate synthase 3 regulatory subunit; Reviewed.	4.7155e-91
NZ_CP023445.1|WP_015804711.1|6929126_6930140_-|ketol-acid-reductoisomerase	gnl|CDD|235491	PRK05479, PRK05479, ketol-acid reductoisomerase; Provisional.	0

Protein sequences

>NZ_CP023445.1|WP_096496672.1|6919325_6920939_-|citramalate-synthase
MTTLGDSFHVYDTTLRDGAQREGITYSVTDKLQVARLLDGLGVGFIEGGWPGAMPKDTEFFARAASGELELANAQLVAFGATRKAGVKVQDDPQVRALLDSGAPVVTLVAKSDLRHVERALRTDAAENLAMVHDTVKHLVDNGRRVFLDAEHFFDGFAHDPDTALRVLEAGVTGGADVVVLCDTNGGQLPLGLAEVVADVLARTGFRVGIHCQDDTSCAVANTLAAVQAGATHVQCTANGYGERAGNADLFAVVGNLVTKLGMPVLPEGAVGELTRVSHALAEIANIAPDTHQAYVGSSAFAHKAGLHASAIKVDPLLYNHIDPEVVGNGMKILVTEMAGRASLELKGRELGVDLAANPEALTSAVRKVKELEAGGWSFEAADASLELLLRDELSELDAPPFTLESYRVVLDHRSDGEIVSEATVKVHVGGERVIATAEGNGPVHALDGALRKALLPHLSWLDAVKLNDYKVRILSGDGRDADGAGGTEAVTRVLVNSTDGEREWTTVGVHGNIVEASWLALCDALAHKAAHASALV
>NZ_CP023445.1|WP_096496671.1|6918626_6919280_+|hypothetical-protein
MEPLRGHRLRSPARSALLIAVLLLLAASPAAAATTLQIGTTVRLASDEQCANGFNVEDHLLLPPDCVPRAQGVNPIGVAVRSAEGETIARITQASGRVVLARQVQGVTVTRVPVVQHTGTRITGATAAGIGRRVCVLSRVGGTLCGPVVALNRTVNWAGGTVTGLSEVRVCASGPWGWAPVVDGSLAVGHVLGGAGCSVYFLPIAPLLASGGLRLAL
>NZ_CP023445.1|WP_096498066.1|6917799_6918570_-|fumarylacetoacetate-hydrolase-family-protein
MRIARIAQPDGLAFAAIEGEGDDLVAAEIADEPFGKPTFTGRRWPLADVRLLAPFLPPKIVCVGRNYADHAAELGNEVPAEPLIFLKPNTTVVGPNAEIRLPAASERVEFEGELAVVIGVGGRDIPVERAMGSVLGYTIANDVTARDIQRSEVQFTRAKSYDTFCPLGPWVETEFDPTDVAIRTELDGEVKQDGRTSQLVHDIPALISFISTVMTLRPLDVILTGTPAGVGPMRPGQRVSVTIDGLGTLTNTAAAR
>NZ_CP023445.1|WP_096496670.1|6916341_6917574_+|FAD-dependent-oxidoreductase
MTRTSIAIAGGGPAGMVLGLLLARAGVRVTVLEKHGDFLRDFRGDTVHASTLGLLDDLGLGPAFDAIPPRYVERMRVVAPGGAATVADMRRLPGRHKRIGFVPQWDLLELLARAGRAEPAFTLVMNAEVTGLLREGSKVTGVRYRTPGGEVSLGADVVVAADGRTSRVRAEAGLAVRSFGAPMDVWWFRVPVREGDELGEVLGRFGRGEALVAIPRTGYFQCAFLIRKGTDARLRAEGVERFRGRVAALMPALADRVGEIASLDDVKLLDVRQNRLRTWHRDGLLCVGDAAHAMSPVGGVGINLAIQDAVAAARLLAGPALRGAVTPDVLRRLRRRRLFATAATQAAQRVLQRAVMREPGASERPARVPLPLRVAQRFPVLQAVPAYLVSIGLRPEPTPGFARRSPAPAR
>NZ_CP023445.1|WP_096496669.1|6914762_6916253_-|glutamate--tRNA-ligase
MSTASAPQEVRVRFSPSPTGTPHVGLIRTALFNWAYARHTGGKVVFRIEDTDAARDSEESYLALLDAMRWLGLDWDEGPEVGGPHEPYRQSQRREIYADIARRLLEAGELYESFTTPDEVEARRRAAGQDPKLGYDGFDRDLTDEQKAAYREQGREPVLRLRMPDEDLSWTDLVRGEITFKAGTTPDPVLVRANGDPLYPFTNPVDDALMGITHVLRGEDLLPSTPRQIGLYRALQRIGVTTFTPLFGHMPYVMGEGNKKLSKRDPQSNLFLYRDRGFLPEGLLNYLALLGWSIADDRDIFTTQELVAAFDIAKVSANPARFDLKKAEAINATHLRALPVEEFVSRSLPHLVADGVLPAEPAEADLAVLRGVAPLVQERLVVLSEVSGMVRFLFTADDVFTPEEDSAAKALGADAKPVLEAAVAALEATAEWNAASIEEALKASLVDGLGLKPRKAYAPVRVGVTGRTVSPPLYESMELLGRDRSIGRLRKALGAS
>NZ_CP023445.1|WP_096496668.1|6913920_6914604_-|HAD-family-hydrolase
MCLDVDDTLVDYSTSSRAALASMVGSDDTFPLWQRITDDHCARMLTGEFEYSTMRNIRTRAFFAALGEELDEHEATRRELGRQEALAGSWRLYPDVVPCLDWLRAAGLPLAAVSNASGRHQRDKIAALGLAQYFDTVLIAGEVGAAKPDRVIFDTACAGLNTALADTVHVGDRLYADAIGARDAGMRGVWLDRGGQGDGSLPHGVSAIHSLAELPELLVCELAGTRV
>NZ_CP023445.1|WP_041838493.1|6912442_6913105_+|IclR-family-transcriptional-regulator
MAVLNAVAKDPCGLAELCNRTGLPRATAHRLAVGLEVHRLLRRGSDGRWRPGAALAELAGGATDPLLDAATSVLPRLRDITGESVQLYRRDGMQRVCVSAAEPPSGLRDTVPVGARLPMTAGSGAKVLAAWSDPGTQRAILADAVYGERTLLEVRRRGWAQSVAEREPGVASVSAPVRDSSGTVVAAISVSGPIDRMGRRPGARWAADLLAAAEALQSRL
>NZ_CP023445.1|WP_096496667.1|6910921_6912325_-|3-isopropylmalate-dehydratase-large-subunit
MSRTLAEKVWEAHVVRHGSGAEPDLLYIDLHLLHEVTSPQAFDGLRLAGRRLRRPDLTIATEDHNVPTVDIELPIADPVSRTQVETLRRNCAEFGVRLHPMGDAEQGIVHVVGPQLGLTQPGMTVVCGDSHTSTHGAFGALAFGIGTSEVEHVMATQTLPLRPFKTMAINVEGTLKPGVTAKDVILAVIAKIGTGGGQGYVLEYRGSAISALSMEARMTVCNMSIEAGARAGMIAPDQTTFDYIKGRPHAPSGADWDAAVEYWSTLATDEGAEFDAEVTLDADELTPFVTWGTNPGQGLPLGASVPDPEAIADENERVAAEKALAYMGLEAGTPLREIRVDTVFLGSCTNGRIEDLRAAADVLRGHHVADGVRMLVVPGSMRVRAQAETEGLHEVFQAAGAEWRQAGCSMCLGMNPDQLKPGERSASTSNRNFEGRQGKGGRTHLVSPLVAAATAVRGTLSSPADLV
>NZ_CP023445.1|WP_096496666.1|6910304_6910907_-|3-isopropylmalate-dehydratase-small-subunit
MEAFSTHTGVGVPLRRSNVDTDQIIPAVYLKRVTRSGFEDGLFAAWRGDEHFVLNQEPFRAGSVLVAGPDFGTGSSREHAVWALMDYGFRVVVSSRFADIFRGNSGKQGLVAAQCEQSDVEQLWKVLENEPGASVTVDLERKTVSAKDFTAPFDIDDYTRWRLLEGLDDIALTLRHSDSIAEFESTRAAWLPDTGVRPAS
>NZ_CP023445.1|WP_096496665.1|6909224_6910097_-|HU-family-DNA-binding-protein
MNKAQLIEALAERLGDKKNAAAAVDGIVDVIVRSVHKGEKVNITGFGVFEKRARAARTARNPRTGETVKVKKTNVPAFRAGSTFKDVISGAKKLPRVTAAKPAATATAAKATTTAAKPATTATKAPAAKATTTRTARSTTTRAAAATKAPARRTATAAAKTSATTAKAAPAAKTAAAKAPATKAAATKAAPKTATTAKRTTTAKTAATKAASTSATATKPAATKPVAAKAAPAKATATKAASTKTAAAAKTAAPAAAATTEKPAAKATPAAKTSAAKRTTTRKTATAAKK
>NZ_CP023445.1|WP_096496673.1|6921678_6922716_-|3-isopropylmalate-dehydrogenase
MRLAVIPGDGIGPEVVAEALKVLGEVVPAAEITRYDLGAARWHATGELLPESVLGELRQHDAILLGAVGDPSVPSGILERGLLLRLRFELDHHVNLRPARLYPGVRSPIADPPEIDMVVVREGTEGLYAGNGGLLRKDTPHEIATEVSINTSFGVERVVRDAFARAANRPRKHLTLVHKTNVLTHAGSLWSRVVEEVSLQHPDVTVAYQHVDAATIHLVTDPGRYDVIVTDNLFGDILTDLAAAVTGGIGLAASGNLDVTRRNPSMFEPVHGSAPDIAGQGVADPTAAVLSVALMLDHLGEHEAARRIEASVAFDLATRDHASPGATYAIGDRLAALVSSNVRTG
>NZ_CP023445.1|WP_096496674.1|6922998_6926277_-|S8-family-serine-peptidase
MIPVFAAVLLTGSLSGAALAAEGPQATTPSVKPARGLDAAKLQTKVAGRLASAKGAVTAFVELEAKPAVDTFTEKTGQGASKQQAKEAAKATKGETTKVTDQVVGDLRAKDSGTKELFRTANGVPGVVVTADAAKVRELASRSDVKSIRTVVPKTRTNSSAVQLTNTAKAWQQYGKLGDGTRVGIIDTGIDYTHAAFAGPGTPEAYRAIDPNVVDASYFPTAKVVGGYDFVGDAYDGGSDDPALSTPKPDPNPLDCNDHGTHVAGTAAGFGVNADGSTFTGDYTTLSGEQLDAMRIGPGTAPKALLYALKVFGCDGSTNVTAQALDWALDPDGDGDFTDHLDVVNLSLGSDYGAPDDPDSLFVRKLNAAGVLTVFSAGNGGDLYDIGGSPGSTPEALTVASTRDAFVLRDAAEANGAKQAGQYSQNFDYAGYDQTKPVLALTDPSNLDGCQPFSAADAAAVAGKFVWLEWDDVDATRRCGSGARANNATAAGAVGALFTSALENFNAGIAGNAAIPVFQFTGTATSALRPALAAGALSVRQAGDLRTSLPTYDQKIADTPSAFTSRGVRGPVVKPDVAAPGDTIASALVGSGNGTLVISGTSMAAPHTTGIAALVRQAHPDWTTEEVKAAVMNSAGSDVKENGKTFAPNRVGAGRIDAKAALDNQVLAYVQDDPGAVSASFGPVEVTGKTALTKTIKVVNKSPRAVEYSVGYEAVTSIPGVRYELSEQTVRLSPRGIARVKVTLRIDDPKALAKTVDPTVEPLHLDVPRQFLADASGRVVLSPKSGATVPLRVPVYSAPKPASDISVPGSVKLGKNATQTVLNLTGRGVDQKGFRSLVSVLELQATSPRLPECKRNVTSGCTLNQTAKGADLRHVGVTSTAPLAKLQGNPEEALLAFGVSTWDNWYNLGSNTIFYIDVDVNGDGTPDFETYTTKLTDTDLLVAVTVDLATGETVDIQPVNAQFGDVDTNVFDTNVVVLPVLLSALGIDPSGDTAKITYTVNSTGFYLAPGASDDRIDSIDGALSFDALKPGLWVQGGGDAALSYQAKPGTALVVNREPGTASDSLMVVNHHNASGDRVDVVKVKGGSDRPAV
>NZ_CP023445.1|WP_096496675.1|6926713_6928312_-|phosphoglycerate-dehydrogenase
MSNTSRPVVLIAEKLAPSVLDVFGEDIEVRHVDGTDRPALLSAVADADALLVRSATKVDAEVFAATSKLKVVARAGVGLDNVEVPAATERGVMVVNAPTSNIVSAAEHAVALLLSVARQIPAAHATLAGGAWKRSSFNGVELNGKTVGVVGLGKIGQLFAARLAAFGTSIIAYDPYVAAARAAQLGIELVSLEELLERADAISIHLPKTPETKGLIGAEQLAKTKRGVIVVNAARGGLIDEDALAEAVRSGQVGGAGIDVFATEPTTASPLFGLPNVVVTPHLGASTSEAQDRAGTDVAKSVLLALAGDFVPDAVNVQGGGVVGEEVRPYLPLVQKLGTVVAALSAKAPTSVTLEVRGELSNEDVSVLPLAALRGVFSSVVEEQVTFVNAPALAASLGVSVDVVKEPSSANHRSLVTVRAVQADGSVLTVSGTLTGLDQVEKIVGVNGRSFDLRAEGNVLLLEYSDRPGVMGTVGTLLGEAGVNVEAAQISQQKGGSEALMLLRVDRPVDSNVLDPIGASVGARTMRSVDFG
>NZ_CP023445.1|WP_096496676.1|6928744_6929014_-|DUF397-domain-containing-protein
MSESAPIYDDKAHVRGNLDLSAAQWLRSDEGAEHEAEHVEIAFVEHTDGVTYTAMRNSAEPDGTVLVFTPAEWEAFILGVKDGEFDEPW
>NZ_CP023445.1|WP_015804711.1|6929126_6930140_-|ketol-acid-reductoisomerase
MSVEIFYDDDADLSVIQGRKVAVIGYGSQGHAHALSLRDSGVDVRIGLPEGSKSRAKAEEQGLKVGTPAEVAAEADLIMILAPDTAQRHIYANDIAPNLKDGDALFFGHGFNIRYGLIQAPSNVDVAMVAPKGPGHLVRRQFVDGKGVPALIAVEQDASGTAQALALSYAKGIGGTRAGVIKTTFKEETETDLFGEQAVLCGGASALVQAGFEVLTEAGYAPEVAYFECLHELKLIVDLMYEGGIARMRYSISDTAEYGDLTRGPRVITPAVKEEMRKVLTEIQDGTFAKEWVEEDDKGRGNYKKLQQDGEVHPIEEVGKKLRGLMSWVDRPLTDTV
>NZ_CP023445.1|WP_015804712.1|6930197_6930704_-|acetolactate-synthase-small-subunit
MTKHTLSVLVEDKPGVLARVAGLFSRRGFNIESLAVGRTEHPDISRMTIVVAVEELPLEQVTKQLNKLVNVIKIVELETAASVQRQLLLVKVRADATVRSQVLETVQLFRAKVVDVSPEAVTVEATGTSEKLDALLRMLEPYGLREIVQSGMVAIGRGARSITATAVR
>NZ_CP023445.1|WP_096496677.1|6930752_6932588_-|acetolactate-synthase-large-subunit
MTSATSRPAPGEPLSPRPGPRPKPAPPSGAPVRVTGAQSLVRSLEAVGCEIVFGIPGGTILPAYDPLLDSTKVRHVLVRHEQGAGHAATGYAQATGRVGVCMATSGPGATNLVTPLADANMDSVPVVAITGQQSRPLIGTDAFQEADICGITMPITKHNFLVTDPADIPRAIAEAFHIAATGRPGPVLVDIPKDVLQETTSFSWPPELRLPGYRPTTRPHGKQVREAAKLIAAARRPVLYVGGGVIKAEASAELLRLAEENDIPVVTTLMARGAFPDSHRQHLGMPGMHGTVSAVAAMQKADLLIALGARFDDRVTGQLESFAPEAQVVHADIDPAEISKNRRADVPIVGDCKEIITELIDAVANEKAHGHAADLTPWWELIDSWRGTFPLGYDWPDDGTLSPQYVIERIGALSPDAVYTAGVGQHQMWAAQFVKYESPRTWINSGGLGTMGYAVPAAMGAKAGVPDRTVWAIDGDGCFQMTNQELATCAIEGIPIKVAVINNGNLGMVRQWQTLFYGERYSNTDLGTHKHRIPDFKLLAEAMGCAGLRAESREEVDAVIKQALEINDRPVVIDFTVGKDAQVWPMVAAGTGNSEIMAARGIRPLFEEDDV
>NZ_CP023445.1|WP_157767898.1|6932879_6933476_+|PH-domain-containing-protein
MPKLVFRVPATALLASGLTAICVTPMALAEPVLSVLYLLPLGFAWWVVRTRTTATPERLVTRTAFGGRVVEWDEVRSLKVSGKGGLSAVVADEELVELPAVKLAHLPALAAVSGGRVDDPVARAKALAEAEEARAEAGAGEAGESAEPAETTDQVSPEQVKKDTADAEQSPEQLTGQPAEQSPEQPAGKPVAKPADDA
>NZ_CP023445.1|WP_096496679.1|6933611_6934031_+|vitamin-K-epoxide-reductase-family-protein
MTQKSRLAFLILSLLGLATSVYLTVTHFQQELLVCSENSLVDCGTVTSSEQSELFGVPVAVLGALFFAFLTAISLPWAWRVPPLRWVRLGAVGVGVLLVVYLVAAEFLLIGKVCLWCTVVHVVTLAQAGVLVRGELKQG
>NZ_CP023445.1|WP_096496680.1|6934147_6935992_+|dihydroxy-acid-dehydratase
MPPLRSRTTTHGRNAAGARALWRATGMTDSDFGKPIVAIANSYTQFVPGHVHLRDLGDIVAEAIREAGGVPREFHTIAVDDGIAMGHSGMLYSLPSREIIADSVEYMVNAHQADAIVCISNCDKITPGMLNAAMRLNIPVVFVSGGPMEAGKAVVVDGVAVAPTDLITAISASASPEVDDEGLSVVERSACPTCGSCSGMFTANSMNCLTEALGLALPGNGSTLATHAARRELFSEAGRVVVELCKRYYGEDDESVLPRSIANRAAFENAMALDMAMGGSTNTVLHILAAAQEGEVEFDLSDINALSRRVPCLAKVSPNSDYHMEDVHRAGGIPALLGELYRAGLLNEDVTTVHSRTMAQWLGEWDIRAESPSERAVELFHAAPGGVRTTQAFSTSNRWSKLDTDAAGGCIRDVEHAYTKDGGLAVLHGNLAESGAVIKSAGIDEELWRFEGPARVVESQEQAVSVILNKEIQAGDVLVVRYEGPSGGPGMQEMLHPTAFLKGAGLGKKCALITDGRFSGGTSGLSIGHVSPEAAGGGLIGLVQDGDRILIDVHERKLELLVDEAVLADRRAKMEASERPWQPVDRVRPVTAALRAYARMATDASKGAVRDVNR

Crispr_ID: NZ_CP023445_13

• CRISPR_ID: NZ_CP023445_13
• CRISPR_location: 6969378-6969625
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP023445_13

Consensus_repeat	Method
GATCGGCCGTCGAGCGATCGGCT	CRISPRCasFinder

spacers of NZ_CP023445_13

>13.1|6969401|22|NZ_CP023445|CRISPRCasFinder
TCCCGGCCCTCAACGGCTGGAC
>13.2|6969446|22|NZ_CP023445|CRISPRCasFinder
GCCAGGCCCTCAACCGCTGATT
>13.3|6969491|22|NZ_CP023445|CRISPRCasFinder
GTCGAGCGATCGGCTGTCGAGT
>13.4|6969536|22|NZ_CP023445|CRISPRCasFinder
ATCGGGCGATCGGCCGTCGAGC
>13.5|6969581|22|NZ_CP023445|CRISPRCasFinder
GTCGAGCGATCGGCTGCTGGGC

CRISPR arrays and Neighbor proteins around NZ_CP023445_13

CRISPR arrays

The CRISPR arrays of NZ_CP023445_13

>merge|NZ_CP023445|13|6969378-6969625|CRISPRCasFinder
GCTCGGCCGCCGGACGCTCGGTTTCCCGGCCCTCAACGGCTGGACGCTCGGTCGTCGGCTGCTCGGCCGCCAGGCCCTCAACCGCTGATTGCTCGGCCGCCGGGCGGTCGACCGTCGAGCGATCGGCTGTCGAGTGATCGGCCGTCGAGCGATCGGCTATCGGGCGATCGGCCGTCGAGCGATCGACTGCTGGGCGATCGGGCGTCGAGCGATCGGCTGCTGGGCGATCGGGCGTCGGGTGATTGGTC

>NZ_CP023445|13|12|6969378-6969625|CRISPRCasFinder
GCTCGGCCGCCGGACGCTCGGTT	TCCCGGCCCTCAACGGCTGGAC
GCTCGGTCGTCGGCTGCTCGGCC	GCCAGGCCCTCAACCGCTGATT
GCTCGGCCGCCGGGCGGTCGACC	GTCGAGCGATCGGCTGTCGAGT
GATCGGCCGTCGAGCGATCGGCT	ATCGGGCGATCGGCCGTCGAGC
GATCGACTGCTGGGCGATCGGGC	GTCGAGCGATCGGCTGCTGGGC
GATCGGGCGTCGGGTGATTGGTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096496710.1|6970787_6971576_-|hypothetical-protein	unknown	unknown	gnl|CDD|143586
NZ_CP023445.1|WP_096496701.1|6959059_6959296_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496712.1|6972721_6974221_+|glycoside-hydrolase-family-57-protein	unknown	unknown	gnl|CDD|224460
NZ_CP023445.1|WP_096496705.1|6964324_6965095_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|225717
NZ_CP023445.1|WP_096496714.1|6975734_6976016_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496718.1|6979258_6980410_-|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|380115
NZ_CP023445.1|WP_096496717.1|6978284_6979217_+|nucleoside-hydrolase	unknown	unknown	gnl|CDD|239117
NZ_CP023445.1|WP_096496707.1|6966300_6967080_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	unknown	unknown	gnl|CDD|224997
NZ_CP023445.1|WP_096496715.1|6976012_6976807_-|GAF-domain-containing-protein	unknown	unknown	gnl|CDD|224867
NZ_CP023445.1|WP_096496702.1|6959370_6960459_-|tRNA-2-thiouridine(34)-synthase-MnmA	unknown	unknown	gnl|CDD|234664
NZ_CP023445.1|WP_096496704.1|6963332_6964325_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_CP023445.1|WP_096498069.1|6977002_6977431_-|protein-tyrosine-phosphatase	unknown	unknown	gnl|CDD|350355
NZ_CP023445.1|WP_096496706.1|6965320_6966280_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	unknown	unknown	gnl|CDD|224936
NZ_CP023445.1|WP_096496703.1|6960464_6961640_-|cysteine-desulfurase	unknown	unknown	gnl|CDD|224029
NZ_CP023445.1|WP_096496713.1|6974447_6975701_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_CP023445.1|WP_096498068.1|6961639_6962965_-|MFS-transporter	unknown	unknown	gnl|CDD|341045
NZ_CP023445.1|WP_096496708.1|6967335_6968178_+|DegV-family-EDD-domain-containing-protein	unknown	unknown	gnl|CDD|273257
NZ_CP023445.1|WP_096496711.1|6971978_6972725_+|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|369777
NZ_CP023445.1|WP_096496700.1|6958550_6958904_-|hypothetical-protein	unknown	unknown	gnl|CDD|372110
NZ_CP023445.1|WP_096496716.1|6977466_6978213_-|acetyltransferase	unknown	unknown	gnl|CDD|100053

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096496710.1|6970787_6971576_-|hypothetical-protein	gnl|CDD|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	0.000136701
NZ_CP023445.1|WP_096496715.1|6976012_6976807_-|GAF-domain-containing-protein	gnl|CDD|224867	COG1956, COG1956, GAF domain-containing protein [Signal transduction mechanisms].	0.000391178
NZ_CP023445.1|WP_096496712.1|6972721_6974221_+|glycoside-hydrolase-family-57-protein	gnl|CDD|224460	COG1543, COG1543, Uncharacterized conserved protein [Function unknown].	5.73245e-141
NZ_CP023445.1|WP_096496705.1|6964324_6965095_-|GNAT-family-N-acetyltransferase	gnl|CDD|225717	COG3176, COG3176, Putative hemolysin [General function prediction only].	2.82635e-54
NZ_CP023445.1|WP_096496718.1|6979258_6980410_-|SAM-dependent-methyltransferase	gnl|CDD|380115	pfam18096, Thump_like, THUMP domain-like. This is a domain of unknown function found in bacteria.	3.61365e-15
NZ_CP023445.1|WP_096496707.1|6966300_6967080_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	gnl|CDD|224997	COG2086, FixA, Electron transfer flavoprotein, beta subunit [Energy production and conversion].	6.89616e-87
NZ_CP023445.1|WP_096496717.1|6978284_6979217_+|nucleoside-hydrolase	gnl|CDD|239117	cd02651, nuc_hydro_IU_UC_XIUA, nuc_hydro_IU_UC_XIUA: inosine-uridine preferring, xanthosine-inosine-uridine-adenosine-preferring and, uridine-cytidine preferring nucleoside hydrolases. 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 proteins similar to nucleoside hydrolases which hydrolyze both pyrimidine and purine ribonucleosides: the inosine-uridine preferring nucleoside hydrolase from Crithidia fasciculata, the inosine-uridine-xanthosine preferring nucleoside hydrolase RihC from Escherichia coli and the xanthosine-inosine-uridine-adenosine-preferring nucleoside hydrolase RihC from Salmonella enterica serovar Typhimurium. This group also contains proteins similar to the pyrimidine-specific uridine-cytidine preferring nucleoside hydrolases URH1 from Saccharomyces cerevisiae, E. coli RihA and E. coli RihB. E. coli RihA is equally efficient with uridine and cytidine, E. coli RihB prefers cytidine over uridine. S. cerevisiae URH1 prefers uridine over cytidine. .	1.57673e-100
NZ_CP023445.1|WP_096496702.1|6959370_6960459_-|tRNA-2-thiouridine(34)-synthase-MnmA	gnl|CDD|234664	PRK00143, mnmA, tRNA-specific 2-thiouridylase MnmA; Reviewed.	0
NZ_CP023445.1|WP_096496704.1|6963332_6964325_-|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.	1.75567e-29
NZ_CP023445.1|WP_096498069.1|6977002_6977431_-|protein-tyrosine-phosphatase	gnl|CDD|350355	cd14505, CDKN3-like, cyclin-dependent kinase inhibitor 3 and similar proteins. This family is composed of eukaryotic cyclin-dependent kinase inhibitor 3 (CDKN3) and related archaeal and bacterial proteins. CDKN3 is also known as kinase-associated phosphatase (KAP), CDK2-associated dual-specificity phosphatase, cyclin-dependent kinase interactor 1 (CDI1), or cyclin-dependent kinase-interacting protein 2 (CIP2). It has been characterized as dual-specificity phosphatase, which function as a protein-serine/threonine phosphatase (EC 3.1.3.16) and protein-tyrosine-phosphatase (EC 3.1.3.48). It dephosphorylates CDK2 at a threonine residue in a cyclin-dependent manner, resulting in the inhibition of G1/S cell cycle progression. It also interacts with CDK1 and controls progression through mitosis by dephosphorylating CDC2. CDKN3 may also function as a tumor suppressor; its loss of function was found in a variety of cancers including glioblastoma and hepatocellular carcinoma. However, it has also been found over-expressed in many cancers such as breast, cervical, lung and prostate cancers, and may also have an oncogenic function.	5.89468e-08
NZ_CP023445.1|WP_096496706.1|6965320_6966280_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	gnl|CDD|224936	COG2025, FixB, Electron transfer flavoprotein, alpha subunit [Energy production and conversion].	5.46322e-108
NZ_CP023445.1|WP_096496703.1|6960464_6961640_-|cysteine-desulfurase	gnl|CDD|224029	COG1104, NifS, Cysteine sulfinate desulfinase/cysteine desulfurase and related enzymes [Amino acid transport and metabolism].	1.71827e-169
NZ_CP023445.1|WP_096496713.1|6974447_6975701_+|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	3.30203e-78
NZ_CP023445.1|WP_096498068.1|6961639_6962965_-|MFS-transporter	gnl|CDD|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.18912e-28
NZ_CP023445.1|WP_096496708.1|6967335_6968178_+|DegV-family-EDD-domain-containing-protein	gnl|CDD|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	3.05458e-72
NZ_CP023445.1|WP_096496711.1|6971978_6972725_+|SAM-dependent-methyltransferase	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	5.38989e-23
NZ_CP023445.1|WP_096496700.1|6958550_6958904_-|hypothetical-protein	gnl|CDD|372110	pfam12441, CopG_antitoxin, CopG antitoxin of type II toxin-antitoxin system. CopG antitoxin is a member of a type II toxin-antitoxin system family found in bacteria and archaea. Most antitoxins encoded by the relBE and parDE loci belong to the MetJ/Arc/CopG family of dimeric proteins which bind DNA through N-terminal ribbon-helix-helix (RHH) motifs. The toxin for CopG proteins falls into the family BrnT_toxin, pfam04365.	9.19146e-05
NZ_CP023445.1|WP_096496716.1|6977466_6978213_-|acetyltransferase	gnl|CDD|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	1.31879e-33

Protein sequences

>NZ_CP023445.1|WP_096496708.1|6967335_6968178_+|DegV-family-EDD-domain-containing-protein
MYRRVAIVTDSAACLPERVTDQMGIGVVQIQVRLGDRTDDEARVPVAELVAAMRSGTPVSTAPPDPGAFFWTYSDLAAAGAQAVVSVHVSGALSRTFEAAREAATQARVPVTVVDSGTAGTSLGYAVLAAAAAARAGGDAARVADAARRTAGRCTEVIYVDTLEFLRRGGRVGAAAALLGSAFAVKPLLTVDGGRIVPLERVVGGERALRRAVDVAVRRAGEFEVDVAVEHFDALERAQSVLEELRGRVPRVRQAMLAPVSSAVGAHVGPGAIGVTVSPV
>NZ_CP023445.1|WP_096496707.1|6966300_6967080_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein
MNIVVLVKQVPDTWSERKLSDTDHTLDRDAADAVLDEINERAVEEALVLQAAHGGEVTVLSMGPDRATDAIRKALSMGADKAIHVSDPALHGSDALTTAKVLAKALATVEFDLVIAGNEATDGRAGAVPAILAELLGLPQLTHVRKVTVEGGVVKAVRETDEGVAHLEAGLPAVLSVNEKINEPRYPSFKGIMAAKKKPVTTLTAADLGLGADEVGLGAAWTQVVEAAPKPPRTAGQRVEDEGDGGSKIAEYLVGQKLI
>NZ_CP023445.1|WP_096496706.1|6965320_6966280_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein
MPEVLVLVDHVDGEVKKVTHELLSAARRIGDPAAVVVGSPGVTGKVKDSLARYGAVKVYAAESADADALLVTPKVDALQAVAATASPAAVLISATLEGKEVAGRLAARLGSGLLYDAVDVDADGSVTQSVFGGAFVVKAKSTRGVPVIAVRPGAVEAEEAPAEAAEVAVELPATDAAKVTRVTGREVLVGGDRPELTEATVVVAGGRGVGSAEKFDVVEKLADVLGAAVGASRAAVDSGYYPHQFQVGQTGKTVSPQLYIALGISGAIQHRAGMQTSKTIIAVNKDPEAPIFEIADYGVVGDLFTVVPQLTGEVEKRKG
>NZ_CP023445.1|WP_096496705.1|6964324_6965095_-|GNAT-family-N-acetyltransferase
MTQPQLLVSTGSTAERGAGYSLLVARDGDEVVAAQRLRHRVFAEEMGAALSTPVPGLDIDPFDEFCDHLVVRDDATGEIVGTYRMLPPERAREAGGLYSDTEFDLTALDGLRPQIVETGRSCVHPDHRSGAVVSLVWAGIARYMLLSGHSWLVGCASVPLGDGGAHAAGVWDQVSAKNLAPEEHRVVPRSPWDVDAVARGGRVAVPPLLKGYLRLGAWVCGRPAHDPAFGVADLLVLLSMERVDQRYLKFFLGEVG
>NZ_CP023445.1|WP_096496704.1|6963332_6964325_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MAAHAWMPLSPCGDGCVAEGATVGRARAALRFAGLAGVLAAGALVAPAALVLRGRAREALLRGWFRLMVRASGVEARVVGERRFQGTPGRGVLVVANHVSWLDELVIDSVQPIRIVAKRDIRSWPVLGWVITAARTVYLDRERLRLLPGTVAELAAALRSGAAVGVHAEGTTWCGSESGPFRPALFQAALDAGVPVRPVALRYLRGGVATTRPAYVGADGLLDAIWRVVRTGGLVVEVHVLDEIAPGRAADRRELAALAQSATERVLPPGTAVGAGHRAVVAARAPGMVAPGVPAGVVLPPVVLPPGAASAEVVVPRRGRSGRRRLSRKG
>NZ_CP023445.1|WP_096498068.1|6961639_6962965_-|MFS-transporter
MWAPENRGPVTGMVLLITLLAFEAMGVSTAMPRMVADLDGQAFYSWPFLGFQAASVVAVVLSGRVCDRIGPRLPLLVGPALFVVGLAVAGIAQDMTLLMAGRVLQGLGAGAQIVAVYVLIGLVYPERLRPAVFGALSAAWVVPSLVGPAVAGWLTENLSWRWVFLGLVPLVAVGFALVLPVLRALPPHRGEEPARRGLPLAAFGAGGGVAGLSWAAQHPGWASLALGAASLAVLMPSLRVLLPKGTLTARRGLPVTILARGLLAGTFFAVEAFIPLTLTTVHGYSATAAGIPLTLSALGWSAASVWQSRRTDIPRETLVRWGFTVSAVGIASVTLIAPSWGPAWLTAVLWGIGGLGVGMAMSSLSVLTLAASTDADRGFNSSALQVSDMLGSALLVGLGGVVLAAAPNLTAAVIPLDLLMAALAVLGAVLTGPRCRATLDD
>NZ_CP023445.1|WP_096496703.1|6960464_6961640_-|cysteine-desulfurase
MAYFDHAATTPVLPEAIAALTEALSRTGNASSLHTSGRRARRLVEEAREDIADALGAKPSEVLFTAGGTESDNLAVKGAYWARRREGRNRVVAGAVEHHAVLDAVDWLAEHEGAEVTLVEPDAAGRITPDALRAVLGEDVALVTAMWANNEVGTVNPVAELSAAAAEFGVPLHTDAVQAVGAVPVSFADSGAGALTVSGHKIGAPYGIGALLLGRQVGVTPLLHGGGQERDVRSGTLDVPAIAAFAVAVRHAVERREASAARLRALRDQLVGAVRAAVPDVIVNGDPEDGLPGHAHLTFPGCEGDSLLMLLDARGVECSTGSACTAGVAQPSHVLLAMGVDPVLARGSLRFTLGWTSTEAEVRELAGVIGPVVERARSAGIAGMRRHKAEV
>NZ_CP023445.1|WP_096496702.1|6959370_6960459_-|tRNA-2-thiouridine(34)-synthase-MnmA
MRVLAAMSGGVDSAVAAARAVEAGHDVTGVHLALSAKPGTLRTGSRGCCTIEDSHDARRAADVLGIPFYVWDFAERFTEDVVEDFVAEYAAGRTPNPCLRCNERIKFEALLDKAIALGFDAVCTGHYARLDVVDGLVELRRSADGGKDQSYVLASLTREQLAHAMFPLGGSTKVEVRAEAARRGLSVAAKPDSHDICFIPDGDTQGFLTKRLGQRAGVLVDDETGAVLGQHVGVHGFTVGQRKGLGIDAPAPDGRPRYVLSLEPVSGTVRVGAAERLAVREIVAVRPVSRVDWSGPVECVAQVRAHGGTAPAIAELVGEELVVRLREPLSGVAPGQAVAVYREDPEGGDLVLASATIERTGV
>NZ_CP023445.1|WP_096496701.1|6959059_6959296_-|hypothetical-protein
MFRGVKEGQWSADHIARHDVTLDEVREAILERPHWQEKGKNDTTPICGRAHAGRHSFVVAVDDGGEAFVVSRAGREPR
>NZ_CP023445.1|WP_096496700.1|6958550_6958904_-|hypothetical-protein
MKTTSLRLPADVVDALRELARSRGVRCTALLREIVERALSGSRSAGGEEFARIDRRLARIEASVLGAGPGGAAGRSGGSSVGAPGSHRDRGRSGARATRAVRRKRASGVVRRVAGTR
>NZ_CP023445.1|WP_096496710.1|6970787_6971576_-|hypothetical-protein
MRARGLPLTPLLVGLVVVPASLTGLGFALAEEEITGSLPFAPPREPAPQTSVHPLAGPQPPRSGPTPRGAPFGVGGSTGVGPGGVGPWTTGVGPGGSGTTGAGTTGSGSTGAGSNGAGTTGAGSTGSGTTGSGTAGAVPVDRAGPVAQARREVERVLAEHSATGVEFAPGGVEHAGRGGAVLGRLGDVLGGTGGLAVTLVAHTWPGEAPEGQSSVLALRRAEVVRAALVDRGVPVESIRTRVVADRAREVPGGGPQVDVLVG
>NZ_CP023445.1|WP_096496711.1|6971978_6972725_+|SAM-dependent-methyltransferase
MTVEPLPLTGERTAPGIEAENYWFRRHEAAYLALLRHCAGAVVLEAGCGEGYGAALIAERADRVVALDYDARTAAHAARAYPGLAVVRGNLADLPLRAASVDVVANLQVIEHLWDQEGFLAECARVLRPGGRLLLTTPNRITFSPGRDTPLNPFHTRELAPAELAGLLTGAGFEVEELTGLRHGPRLRALDERFGGSIIDAQVAVVVDGDPWPADLLAAVAGVSAEDFEITPEEMDASLDLVAVAVRP
>NZ_CP023445.1|WP_096496712.1|6972721_6974221_+|glycoside-hydrolase-family-57-protein
MTGAEGTFCLVLHSHLPWLAHHGAWPVGEEWLYQAWAHSYLPVVDLLERFAAEGRRDVLTLGVTPVLAAQLDDPYCLRGVHDWLGNWQLRAHGAAPRLPELAAREHREAAVALERFEGRWRHGFSPLLRPLVDSGVVELLGGPAAHPFQPLLDERLRAFALETGLRDTALRLGSRPEGIWAPECGYAPGMERGYAAAGVRRFLVDGPSLGNETWAGRRVGDSDVVCFGRDLEVSYRVWSPRVGYPGHPDYRDFHTYDHASGLKPSRVTGVEVAPEHKRPYDPEAARAAVRGHTEDFVGAVVARLRELRAAHGREALVVAAYDTELYGHWWHEGPLWLESVLRALPEAGVRVTTLRGAVEAGHVVGSVEVPASSWGAGKDWNTWSGPQVADFVHANAELQRELLGLGLGGAVRDPVADQAVREALLSLSSDWAFMVTKDSAADYARYRAKVHAERFRELAVELRAAREGADLGRVDRARGRAAELRALSGPFGHLDARAL
>NZ_CP023445.1|WP_096496713.1|6974447_6975701_+|glycosyltransferase-family-4-protein
MRVLMLSWEYPPVVVGGLGRHVHALADRLVRAGHEVVVLCRQPEGTDAVTHPTEDVVLGGVRVVRVAEDPAHLVFERDLVAWVLAMGHAMTRAGLALLREGWRPDVVHAHDWLVTHPAVALAEAAQAPLVATVHATEAGRHSGWLSQTLNQQVHSVEWWLANRADELITCSGAMRTEVAHLFEVEPAGITVLHNGIEPKRWRVRAADVEAARGRHSPDGAPVLLFFGRLEWEKGVQDLIAALPRVRRRHPGTRLVVAGTGTHREWLVEQARKHKVKRAVEFAGHLSDRELAAAIAAAAAVVLPSRYEPFGIVALEAAAAGAPLVASTAGGLGEVVLDGETGLSFPPGDVDALARAVCAVLDDRGAAGRRARAAKARLATDFDWGTIAEGTVEVYRAAVVRERGALGRPKIGTGNVFL
>NZ_CP023445.1|WP_096496714.1|6975734_6976016_-|hypothetical-protein
MTFERALDGRTVDDLAADLAAVRRRVSRERARLVLASRALWRVSVCGLVLGAVGHLGAALHLLGSGDDAVVCALGVGVAALFAVAAWRLGRRG
>NZ_CP023445.1|WP_096496715.1|6976012_6976807_-|GAF-domain-containing-protein
MSKKSIPVPVPARYAISVLLPALAAIASAVAAFAEGAARSYGIWGSAICAVGIACWGVLREVWAKREEADALARVKRAKHEVLGAAIPLVKELGKLAVVSADGAGRVPVQVLRNRVVAAARTQCGTDDRENYRAALYLWRDGHLTLADHEGRDGGRAPRAVFLPDGEYERFVLRHARGSDPLFYEDLLEKAPESFGSVSPRSFRSLISVPVHVSGRSFGMLSVDSPEPGSLTPVDRDHMILLAAVLAAGLAAEERDGESLKEAS
>NZ_CP023445.1|WP_096498069.1|6977002_6977431_-|protein-tyrosine-phosphatase
MVVELPDGAVVTGRGLRGGPPEVEPGYGLYLGGARLRAAHDAALTWPHEWVDWPDFLLPRDGGAAVRLIHDLHRRALAGEAVEVACGGGNGRTGTVLACLAVLSGVPRGEAVAWTRAHYRKHAVETPWQKRWVLRFPANDVS
>NZ_CP023445.1|WP_096496716.1|6977466_6978213_-|acetyltransferase
MTSMWGSSTWSRWRGARRDPAQARFLTLASLRWVLRHRAYTPWYLVRYWRLLKFRVANPHVVLRGMVFLGKKVEIHCRPGFGRLEIGRWVHIGDGNAIRCHEGSLRIGDKAVFGKDNTVNCYLDVEIGAATLVADWVYVCDFDHVTSDITLPIKDQGIVKSPVRIGPDCWLGTKVTVTRGTRIGRGCVLGAHAVVRGDVPDYKIAVGIPARVVRDRRADYEAGAGTRAAVADMARKAREALERSRADE
>NZ_CP023445.1|WP_096496717.1|6978284_6979217_+|nucleoside-hydrolase
MTTPLIIDTDPGVDDAFALALAAASPEVDLVGVTTTFGNVGLERTTRNALGLLALLGRADVPVAAGADRPLVHAQPSLSSAHGSDGLSGFAGALPPAGAPDPRDAVALLADLLGASDRPVVIAAVGPLTNVALLLAAHPSLKPKIERLVVMGGAIGAGNISPRAEFNAWCDPEAARRVLVVEDVPTTLVPMDLTMRCSVDGPWLDAVGAASEVGRVLVGMTADYRRAYRGLLGWDGMALHDAVAVAEAVRPGLLTTRRLPVEVDCGYGPGRGSLLVDERLEARDAGRVDVAVDVDVAGLRGWLSERLGGL
>NZ_CP023445.1|WP_096496718.1|6979258_6980410_-|SAM-dependent-methyltransferase
MGYGFSLDDVAYLRSDAGCAALSALSGLPLTDASRLADVAAARREAGEFFAAVLETLLLRRKAPSKVDFVDGLYTDDALQQATAAPVARHRASRFTGPVHDLTCSIGAELAWLPEGSIGSDLDPVRLAMARHNLGPDVGLALADALRPASRGVPLLADPARRDSAGRRTWRPSDFLPPLDGLAQACADRDLAVKCAPGVDFAVAPWADEVEVVSLDGQVREACLWTRGLATPGVSRRATVLRTGGEPWTLTDAEPDDCPVAEPGEWLVDPDGAVVRAGLVRHYAARHGLAQLDEHIAYLTGPVPPPGVRAFRVVEHGRYSEKALRSVLRAHDVGVLEILVRGLDVDPKPLRRKLKLSGSESMAVVLTRVGRSPVYLLARAERT

Crispr_ID: NZ_CP023445_14

• CRISPR_ID: NZ_CP023445_14
• CRISPR_location: 7196262-7196543
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP023445_14

Consensus_repeat	Method
AGGNCTACCAGCAGCAGN	CRT

spacers of NZ_CP023445_14

>14.1|7196280|51|NZ_CP023445|CRT
CGCCGCAGCAGACCGGCTACCACACCCCGCCCCCCGGCTACCCGGCCCAGC
>14.2|7196349|36|NZ_CP023445|CRT
CGGGTCACCAGGGGCAGCCGGGCTACGACCCGCAGC
>14.3|7196403|30|NZ_CP023445|CRT
CCCCGCAGGGTTACCCGCAGCAGCCGCCGC
>14.4|7196451|18|NZ_CP023445|CRT
GCTTCGACCCGCAGCAGC
>14.5|7196487|39|NZ_CP023445|CRT
AGCCGGGTTACCAGGGGCAGCCGGGGTACGACCCGCAGC

CRISPR arrays and Neighbor proteins around NZ_CP023445_14

CRISPR arrays

The CRISPR arrays of NZ_CP023445_14

>merge|NZ_CP023445|14|7196262-7196543|CRT
AGGCCTACCAGCAGCAGGCGCCGCAGCAGACCGGCTACCACACCCCGCCCCCCGGCTACCCGGCCCAGCCGGGCTACCCGCAGCAGCCGGGTCACCAGGGGCAGCCGGGCTACGACCCGCAGCAGGCGTACCAGCAGCAGGCCCCGCAGGGTTACCCGCAGCAGCCGCCGCAGGGCTACCAGCAGCAGGGCTTCGACCCGCAGCAGCAGGCCTACCAGCAGCCGCAGCCGGGTTACCAGGGGCAGCCGGGGTACGACCCGCAGCAGGCCTACCAGCAGCAGG

>NZ_CP023445|14|3|7196262-7196543|CRT
AGGCCTACCAGCAGCAGG	CGCCGCAGCAGACCGGCTACCACACCCCGCCCCCCGGCTACCCGGCCCAGC
CGGGCTACCCGCAGCAGC	CGGGTCACCAGGGGCAGCCGGGCTACGACCCGCAGC
AGGCGTACCAGCAGCAGG	CCCCGCAGGGTTACCCGCAGCAGCCGCCGC
AGGGCTACCAGCAGCAGG	GCTTCGACCCGCAGCAGC
AGGCCTACCAGCAGCCGC	AGCCGGGTTACCAGGGGCAGCCGGGGTACGACCCGCAGC
AGGCCTACCAGCAGCAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096496872.1|7210056_7210794_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496856.1|7185575_7186865_-|bifunctional-o-acetylhomoserine/o-acetylserine-sulfhydrylase	unknown	unknown	gnl|CDD|236105
NZ_CP023445.1|WP_096496874.1|7213383_7213977_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496873.1|7211020_7213387_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|276809
NZ_CP023445.1|WP_096496870.1|7207977_7208970_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381313
NZ_CP023445.1|WP_015804942.1|7207069_7207252_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496858.1|7187988_7188765_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496863.1|7193038_7194145_+|alanine-dehydrogenase	unknown	unknown	gnl|CDD|240630
NZ_CP023445.1|WP_096498088.1|7194836_7195259_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096496861.1|7190272_7190764_+|glutathione-peroxidase	unknown	unknown	gnl|CDD|238207
NZ_CP023445.1|WP_096496869.1|7207342_7207927_-|DUF4232-domain-containing-protein	unknown	unknown	gnl|CDD|379419
NZ_CP023445.1|WP_015804935.1|7192243_7192627_-|glycine-cleavage-system-protein-GcvH	unknown	unknown	gnl|CDD|234918
NZ_CP023445.1|WP_096496857.1|7186988_7187987_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|183212
NZ_CP023445.1|WP_096496868.1|7203334_7207063_+|multifunctional-oxoglutarate-decarboxylase/oxoglutarate-dehydrogenase-thiamine-pyrophosphate-binding-subunit/dihydrolipoyllysine-residue-succinyltransferase-subunit	unknown	unknown	gnl|CDD|237030
NZ_CP023445.1|WP_096496855.1|7184547_7185579_-|homoserine-O-acetyltransferase	unknown	unknown	gnl|CDD|234678
NZ_CP023445.1|WP_096496862.1|7190872_7192240_-|L-serine-ammonia-lyase	unknown	unknown	gnl|CDD|273233
NZ_CP023445.1|WP_096496860.1|7189609_7190029_+|protease-inhibitor-protein	unknown	unknown	gnl|CDD|366264
NZ_CP023445.1|WP_096496871.1|7209026_7210064_-|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl|CDD|225412
NZ_CP023445.1|WP_096496867.1|7197569_7202054_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224055
NZ_CP023445.1|WP_096496866.1|7196685_7197561_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|372253

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096496856.1|7185575_7186865_-|bifunctional-o-acetylhomoserine/o-acetylserine-sulfhydrylase	gnl|CDD|236105	PRK07812, PRK07812, O-acetylhomoserine aminocarboxypropyltransferase; Validated.	0
NZ_CP023445.1|WP_096496873.1|7211020_7213387_-|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.	1.40069e-05
NZ_CP023445.1|WP_096496870.1|7207977_7208970_-|aldo/keto-reductase	gnl|CDD|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	8.89275e-179
NZ_CP023445.1|WP_096496868.1|7203334_7207063_+|multifunctional-oxoglutarate-decarboxylase/oxoglutarate-dehydrogenase-thiamine-pyrophosphate-binding-subunit/dihydrolipoyllysine-residue-succinyltransferase-subunit	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	0
NZ_CP023445.1|WP_096496863.1|7193038_7194145_+|alanine-dehydrogenase	gnl|CDD|240630	cd05305, L-AlaDH, Alanine dehydrogenase NAD-binding and catalytic domains. Alanine dehydrogenase (L-AlaDH) catalyzes the NAD-dependent conversion of pyruvate to L-alanine via reductive amination. Like formate dehydrogenase and related enzymes, L-AlaDH is comprised of 2 domains connected by a long alpha helical stretch, each resembling a Rossmann fold NAD-binding domain. The NAD-binding domain is inserted within the linear sequence of the more divergent catalytic domain. Ligand binding and active site residues are found in the cleft between the subdomains. L-AlaDH is typically hexameric and is critical in carbon and nitrogen metabolism in micro-organisms.	0
NZ_CP023445.1|WP_096496869.1|7207342_7207927_-|DUF4232-domain-containing-protein	gnl|CDD|379419	pfam14016, DUF4232, Protein of unknown function (DUF4232). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 177 and 242 amino acids in length. Many members of this family are lipoproteins.	4.6876e-14
NZ_CP023445.1|WP_096496861.1|7190272_7190764_+|glutathione-peroxidase	gnl|CDD|238207	cd00340, GSH_Peroxidase, Glutathione (GSH) peroxidase family; tetrameric selenoenzymes that catalyze the reduction of a variety of hydroperoxides including lipid peroxidases, using GSH as a specific electron donor substrate. GSH peroxidase contains one selenocysteine residue per subunit, which is involved in catalysis. Different isoenzymes are known in mammals,which are involved in protection against reactive oxygen species, redox regulation of many metabolic processes, peroxinitrite scavenging, and modulation of inflammatory processes.	2.99253e-88
NZ_CP023445.1|WP_015804935.1|7192243_7192627_-|glycine-cleavage-system-protein-GcvH	gnl|CDD|234918	PRK01202, PRK01202, glycine cleavage system protein GcvH.	9.7484e-56
NZ_CP023445.1|WP_096496857.1|7186988_7187987_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|183212	PRK11579, PRK11579, putative oxidoreductase; Provisional.	1.34716e-84
NZ_CP023445.1|WP_096496855.1|7184547_7185579_-|homoserine-O-acetyltransferase	gnl|CDD|234678	PRK00175, metX, homoserine O-acetyltransferase; Provisional.	1.54825e-164
NZ_CP023445.1|WP_096496862.1|7190872_7192240_-|L-serine-ammonia-lyase	gnl|CDD|273233	TIGR00720, hypothetical_protein_NEICINOT_00681, L-serine dehydratase, iron-sulfur-dependent, single chain form. This enzyme is also called serine deaminase and L-serine dehydratase 1. L-serine ammonia-lyase converts serine into pyruvate in the gluconeogenesis pathway from serine. This enzyme is comprised of a single chain in Escherichia coli, Mycobacterium tuberculosis, and several other species, but has separate alpha and beta chains in Bacillus subtilis and related species. The beta and alpha chains are homologous to the N-terminal and C-terminal regions, respectively, but are rather deeply branched in a UPGMA tree. This enzyme requires iron and dithiothreitol for activation in vitro, and is a predicted 4Fe-4S protein. Escherichia coli Pseudomonas aeruginosa have two copies of this protein. [Energy metabolism, Amino acids and amines, Energy metabolism, Glycolysis/gluconeogenesis].	0
NZ_CP023445.1|WP_096496860.1|7189609_7190029_+|protease-inhibitor-protein	gnl|CDD|366264	pfam00720, SSI, Subtilisin inhibitor-like.	7.36979e-31
NZ_CP023445.1|WP_096496871.1|7209026_7210064_-|ImmA/IrrE-family-metallo-endopeptidase	gnl|CDD|225412	COG2856, COG2856, Predicted Zn peptidase [Amino acid transport and metabolism].	3.47978e-17
NZ_CP023445.1|WP_096496867.1|7197569_7202054_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.25929e-165
NZ_CP023445.1|WP_096496866.1|7196685_7197561_+|ABC-transporter-permease-subunit	gnl|CDD|372253	pfam12679, ABC2_membrane_2, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family.	9.79157e-05

Protein sequences

>NZ_CP023445.1|WP_096498088.1|7194836_7195259_+|hypothetical-protein
MDESLRAAVLRRLALLDEAAESGEADSLVPLARAEIHRLADGWRLLLTVHQPDPDGRCRACPGVLRHKKWPCQVWTMAHQHLIGDGVPHRERRRPLRNPFTRQTAFTEPGSAPEPDPEGPEEVTQEIPVVVSKPRHALPD
>NZ_CP023445.1|WP_096496863.1|7193038_7194145_+|alanine-dehydrogenase
MRIAVPREVKNHEYRVALTPAGAHELSARGHEVFVEAGAGLGSAIPDDEYLAAGAKVLASADDVWAEGELVLKVKEPVAEEYPRLREGQVLFTYLHLAADRPLTEALLASGTTAIAYETVQSAGGALPLLAPMSEVAGRLAPQVGAFALMKPSGGRGVLPGGVPGVHPARVVVIGGGVAGLSAATIAVGMGADVEVLDTSVDRLRQIDARFGNRLRTVASTRYAVEQAVLEADLVIGAVLVPGARAPKLVDNALVARMRPGSVLVDIAIDQGGCFADSRPTTHADPTYPVHDSVFYCVANMPGAVPRTSTYALTNVTLPYAAALADRGWREALRADHALALGLNTHRGALTNGPVALAHDLEHAPYPV
>NZ_CP023445.1|WP_015804935.1|7192243_7192627_-|glycine-cleavage-system-protein-GcvH
MPAFPENLLYTADHEWVDWTPGTQEPVSVGITSYAAESLGDIVFVQLPEVGERVTSGQVCGELESTKSVSDLYAPVSGEVVEVNTGAVEDPALVNGDPYGGGWLFKVRVESAEGLLTAAKYAELTGD
>NZ_CP023445.1|WP_096496862.1|7190872_7192240_-|L-serine-ammonia-lyase
MAISVFDLFSVGIGPSSSHTVGPMRAAATFAERLRGVSGQVRRVRVELFGSLGATGHGHGSPKAVLLGLEGNKPEEVDPVAAEARVAEIRAAGALRLGGGAEIAFREPDDLVMHRRKSLPLHPNGMVFEAFDAAGASLDRAEYYSVGGGFVVDEHASGADRIKPDTTPLAHPFRTGDELLDLTASTGLRISEVMLANELAWRSEDEVRRGLLHIWQVMQDCVERGCTEQGVLPGGLKVRRRAAEMRRSLRDEHYATDPLRVMDWVTLFALAVNEENAAGGRVVTAPTNGAAGIVPAVLHYYARFVPGASDDGVVRFLLTAGAVGVLFKENASISGAEVGCQGEVGSACSMAAAGLAEVLGGTATQVENAAEIAMEHNLGLTCDPIGGLVQIPCIERNALASIKAITAARMALRGDGSHFVSLDKVIKTMRDTGKDMKVKYKETARGGLAVNVIEC
>NZ_CP023445.1|WP_096496861.1|7190272_7190764_+|glutathione-peroxidase
MSIHDIAVNTLAGEPSSLGSLRGKALLVVNVASRCGLTPQYSALERLHAKYAPQGFSVVGFPCNQFGGQEPGTAEEIATFCSATYGVTFPMFEKVEVNGENRHPVYEALVESADTDGAAGDVQWNFEKFLLSPDGEVLARFRPRTEPEDEAVVRAVEAALPNA
>NZ_CP023445.1|WP_096496860.1|7189609_7190029_+|protease-inhibitor-protein
MTPIPLLVAAAALAPVLALPAQAAATPDSGPGILPLYQPTVLVLTKVDSGGEHEQALLRCDPPSGTHQRAWQACLALAEVNGHVGRMRDSNQVCTMEYNPIKVSVLGVWRGQTRSFSGEYSNPCVMGSVTKSVFSFEKD
>NZ_CP023445.1|WP_096496858.1|7187988_7188765_-|hypothetical-protein
MSESRWPQLPVIGDVALPERDGALWTPLLDLSRRLPDEHVVIGGVMVYLHGLVAGKPPHRVTRDVDVLFNVLVGGVLPEAVGVLEGLGYRLDPASPADSAHRYLGPCGEQVDVLAPMLRNRRSKPSLVTTPPNRTIEVPAGQEALEHRVVLRAAHGDDAAEIVVPDTARALKLKAAAYAQHHRARPSEAWNSRHLTDLAFLCSVIDDPDAVRDALGTPPVGGHLALAAVLDPPSHSAWTALGEAAEDARLVWEVLREP
>NZ_CP023445.1|WP_096496857.1|7186988_7187987_+|Gfo/Idh/MocA-family-oxidoreductase
MRTALLGFGLGGTAFHAPFLSTAEGLTLSAVVTSRSGEVGSRYPWVEVLGSAEELWSRAADFDLVVVTTPNRLHAAHARAALERGLDVVVDKPFAATAAEARSLADLARARGLLLAPFHNRRWDGDFRTVASLVRNGSLGSVHRFESRFERWRPEVKPGWKESADPEALGSVVYDLGTHLVDQAVALFGRPRSVYAEVRALREGAQAHDDAFLALTHEGGEVSHLWASALANDQGPRFRVLGSRSSFVKHGMDPQEAALRAGELPGGPGWGHDTGPATLGGAPVELERGAYQDFYAAVARRESPVPVGDAIAGLEVVEAAFESARAGRVVEL
>NZ_CP023445.1|WP_096496856.1|7185575_7186865_-|bifunctional-o-acetylhomoserine/o-acetylserine-sulfhydrylase
MTWSFETQQVHAGAAPDPTTGARATPIYQTTSFAFRDTAHGAALFSLAEPGNIYTRINNPTQEVLEQRVAALEGGIAAVAFASGQAAETATILNLARAGDHLVSSASLYGGTYNLLHHTLPKLGITTTFVDDPDDLDAWRAAIRPNTKLLFAETLANPRSNVLDITAVADVAHAAGVPLVVDNTVPTPYLLRPLEHGADIVLHSATKFLGGHGTAIAGVVVDGGRFDFGDAARFPDFNDPDPSYHGLRYWPALGHGAFAAKLRVQGLRDTGAAIAPLTSFLVLQGIETLSLRLERHVANAQALAEWLDGRDEVERVHYAGLPSSPWHALAQRYLPWGAGAIVSFELVGGADAGRAFVDGLELFSQLANIGDVRSLVIHPASTTHSQLTAEQQATSGVTPGLVRLSVGIEAVEDLKADLEAGFRAAKSAR
>NZ_CP023445.1|WP_096496855.1|7184547_7185579_-|homoserine-O-acetyltransferase
MTGWRDGDPAGGRRWHRGALPGLPFRLAYETWGALDEDRSNAVLVLHALTGDSHVAGPAGPGHPTAGWWDGLVGPGLALDTDRWFVVAPNALGGCQGSTGPWDAAPDGRPWGERFPAIGIRDQVAAELGLADALGVRSWAAVVGGSMGGMRALEWAVTAPERVRSLLVLAAPAASSADQIALASAQLHALRLHPEQGMAVARRIAHHGYRTAAELNTRFGRSVQGDGRFAVESYLDHQADKLAKRFDPGSYRVLTEAMNGHDVGRGRGGVRAALGSVTARTLVAGIDSDRLYPLEQQRELAEAIPAAGDLRVVASPYGHDGFLVEEEQVAALLGELLEVRSPR
>NZ_CP023445.1|WP_096496866.1|7196685_7197561_+|ABC-transporter-permease-subunit
MGGLISAEFRKTTTTGLWWGLMIPTVLLALGWALGTGALLQSIGEALTSEDGDVLLGGLLGVSADQWKLSVFGITRSINIATIFPMIFGGLAVASEFNRKTITTTFLTAPNRVSAMTAKMVVYLAWGAIYGLVIVTTVSIGIALTADSGQLPEAGGWFALCAVGVLSTMLMTMFGVGVGALMNSTVGTTVVLVLYMLVIENGLQLVLQFQDLSSVIAFLPNGAANGITGGVAADVFMGNVGVVPDGLKEVLMGAAGAAGALDWWLSTLVFLGWTAVFFAGGWAVTQKRDIT
>NZ_CP023445.1|WP_096496867.1|7197569_7202054_+|ATP-binding-cassette-domain-containing-protein
MFAALPQLRAVSLREAALSRPGGRKRPADLSGDRPSVEIVTNFPGWIRRLASACWQHRSLVVWSVLAAVVGVGLQAAGPLLLKVAVDDAVAGRTDRLALLASVLVGVELLTFGTAFVRRYLGGRLAVDVQHDLRQAVFSSVQRLDGQKQDVLRTGQVVSRSITDLQLVQSLLSMTPLAFGTVAFALASLVAMCWLSPPLTLIALVIVPAVGVVAARTRMTLFPATWSAQQRAADVAQQVEETVTGVRVVKGFGQEAREVAALERRARVLFAERMRAARLTARPSATLNALPYAGQVAVLAAGGWLALRGEVSLGTFLAFASYVAALIGPTRLLASLMVTAQLARAGVERVYELVDSQPAVVDAPDAVDVPDGPVGVRLDGVVFGYARSEPVLSGVSLEVAPGETLALVGTAGSGKSTVSLLLPRFYDVHEGSVSVGGVDVRGLRLGSLRRTVGVVFEEAFLFSDTVRANIAYGRPDATDAEVEAAARAAEAHGFISALPGGYGAVVGERGLTLSGGQRQRVALARALLSDPRVLVLDDATSAVDTATEAAIHRTLASVTATRTTLLVAHRRSSLALADRIAVLDAGRVVDVGAHAELWGRCELYRELLAGPGEAIERVAGAGAAGGGVAEVGMAGAGVAGVAGAGIAGAGVAGAGVAGAGVAGAGVAEAGMTGAGVAESGLAAGPEGGNGAGAVDRASGAAARNGGVSAPWPGADPAGRRADPRRENVASQSAEGSTEQTGERSGADAATSGTRSAPPSGAGSTSSSGAGASPSSGAGSASSSAPTGVTPALWPEVVDDELVLRAENRSVAAPSGGRRGPGTSALAGGAPPTPELVERVRSLPPATEEPRLPGEDPSAPDPGFRLLRLLRPVRWSMVAVGALLLVDTSLAIALPNLVRIGVDRGVGGGEQGALWVVSLVGLLLVAVGWCSTRIGTVLTARVGERLLYLLRVRSYAHLQRLGLDYYEREMAGRIMTRMTTDVDALSSFLQTGLTTFVISVLTVAGIAVALVVTDPGLALVALSVLPVLAVATVLFQRVSSRAYAEARERVSAVNADLQENVSGLRVAQAYTREERSAEAFAARSDAYRRARIRAQRYIATYFPFLALLSGVAQAAVLVVGAYRVADGSLSPGVLLAFVLYLGLFFSPLFQLSGVFDGYQQARVGLTRIGDLLRTPTTVPPAADPAPVERLRGEVELRDVVFRYAGAEEPALDGVSLRVRAGETVALVGETGAGKSTLVKLVARFYDVTGGRVLVDGRDVREYDLGAFRRRLGVVPQEAHLFGGDVAENVAYGRPGATPAEVEEAVRAVGALPVVAALPNGFRQQVGERGQGLSAGQRQLVALARAELVRPDVLLLDEATAALDPATESAVLAASDHLSGSRTTFVVAHRLATAARADRIVVLSGGRVAEEGTHEELLALGGQYARLWAHGAPEHGGAEGGEGSEAGGAEAAGAGAAGAGAADGSAADGGAIAEGAATTGTNGVATTAKAGDAPRG
>NZ_CP023445.1|WP_096496868.1|7203334_7207063_+|multifunctional-oxoglutarate-decarboxylase/oxoglutarate-dehydrogenase-thiamine-pyrophosphate-binding-subunit/dihydrolipoyllysine-residue-succinyltransferase-subunit
MSSSPASQFGPNEWLVEEMYEQFLADPSSVDPAWHDFFADYKSTQRNGSTTTAAPTAATQADTGKAASTGAPAAAKQAASTAPAATTPAAPAPSSAPQPKAAAPAKPAAAPAAKPAPAQAAKAAPVQQAKGPEQKQLRGAAAAIAKNMELSLTVPTATSVRAVPAKLLADNRIVINNHLKRTRGGKVSFTHLIGYAVVRALQAFPNMNRHYAEINNKPHVVTPEHVNFGLAIDLPGKDGSRTLVVASVKGCENMTFTQFWQAYEDLIRKARGGSLTAEDFSGTTISLTNPGTIGTNHSVPRLTAGQGTIVGVGAMEYPAHFQGTSEQALTDMGVSKIITLTSTYDHRIIQGAESGEFLKRVHQLLLGEDGFYDDVFTSLRLPYEPIRWVADIPEGAVDKTARVIELIDAYRTRGHLMADTDPLNYRQRKHQDLDVLSHGLTLWDLDREFPVGGFAGKERMRLRDILGVLRNSYCRTVGVEYMHILDPEERLWIQERVEVPHEKPPATVQKYILSKLNAAEAFETFLQTKYVGQKRFSLEGGETVIPLLDAVLDKAAEHELDEVVIGMPHRGRLNVLANIVGKPISQIFREFEGNLDPGQAHGSGDVKYHLGAEGKYFRMFGDGETKVSLTANPSHLEAVDPVLEGIVRAKQDILDMGGESFPVLPVAMHGDAAFAGQGVVAETLNLALVRGYRTGGTVHVIVNNQVGFTTAPENSRSSKYSTDVAKMIGAPVFHVNGDDPEACYWVAKLAVDYRQAFNKDVVIDMVCYRRRGHNEGDDPSMTQPAMYDVIDTKRSVRKTYTEALIGRGDISVEEAEKALQDFSSQLEHVFNEVRELEKHPIKASPSVEEEQQVPAKLPTGVPREVLERIADAHVELPEGFTPHPRVKPVLERRAKMAREGGIDWAYAELLAFGSLVHEGRTVRLAGQDSRRGTFTQRHATLIDRKTGQEYTPIQNLADDQGKFMVYDSVLSEFAALGFEYGYSVANPDALVLWEAQFGDFVNGAQPIIDEFISSGEAKWGQVSDVVLLLPHGHEGQGPDHTSGRIERFLQLCAEGSMTIAVPSTPANYFHLLRRHALDGVNRPLVVFTPKSMLRLKAAVSPVEDFVEERFKSVIDDAAIEDSSAVTKVLLCSGKIYYELVAEREKRGAKDTAIVRVEQLYPVPKRKLNEALEAYPNATDVRWVQEEPANQGAWTFYGLHLPELLPERYRLTRVSRRRMAAPSAGSSKVHEVEQREIITKAFE
>NZ_CP023445.1|WP_015804942.1|7207069_7207252_+|hypothetical-protein
MYFTDRGIEELESRRGEEEVSLAWLADKLRGFVDANPEFETAVERLATYLARDDEDDPED
>NZ_CP023445.1|WP_096496869.1|7207342_7207927_-|DUF4232-domain-containing-protein
MRRTTRTTAMVSLLAACAAVTACGSSTPGSASPGSGSGDGSAVVSTEPAPSSQAPTGQAGDGQAAAAECASLTPSTGKPQGDAQKKLPVVITNTGDTACTLSGFPGAQLVGADGHTWDLTRSSDTTPEVTLQPGEAATSYLSFLPASADPWDVKTLRVTPPNTTATVDLPWAFGPVALQDGATRPGSYIGPVNG
>NZ_CP023445.1|WP_096496870.1|7207977_7208970_-|aldo/keto-reductase
MDYTHLGRSGLSVSRICLGTMNFGPVASETDSHAIMDRALEHGINLFDTADVYGWKTGEGVTEQIIGRWFAQGGGRRDKTVIATKAHNSMGDWPNETHLSALHIRKACDASLRRLNTDYIDLYQMHHVDRSTPWEEIWEAFSVLRQQGKVVYFGSSNFAGWHIAQAQEAARSRGFLGLVSEQSVYNLANRFAELEVLPAARHYGLGVIPWSPLAGGVLGGVLRKRREGTANRGVDDYAKGDLAKLERSLEAYEALCEELGEHPAHVGLAWLLHQEGVTAPLVGPRTVEQLDGSLRAVEIQLDAEVLAKLDELFPAPGPNGSKPAPEAYAW
>NZ_CP023445.1|WP_096496871.1|7209026_7210064_-|ImmA/IrrE-family-metallo-endopeptidase
MPELVPTRLTQARHLAGLTRRGLADLVGVTPTAVGQYEQGAHRPRPALLAALAAALDVPTPFLTADRPHPRLDPASAHFRSLRATRSYQRAKAVAHAEQTWELASALERRAPLPAVDLPRLPGDPVAAARALRAAWRLGAGPVRDLVRRMEERGVLVQCPPRDPDLETVDAFSTAAPHRPVVVLTPNRADDVHRHRFSAAHELGHLVLHGDRAPGGAAGERAADVFAAEFLAPADAIRPELPRRADLRRLAELRRAWGVSATCLLRRCHELGLLSDSAAGRAHLRLRASPEFEPSPLAGHPGEQPAALRGAFEAAHGPARDAAVTALAAELSWRPARVRELLALP
>NZ_CP023445.1|WP_096496872.1|7210056_7210794_-|hypothetical-protein
MKDFEPSEWALAQFGDQAKAVITSVVVGLHRAQQAAWRVQAAATAEGIRNKRAYGSMWDSRYNLVVQQFDLAHLPGYRPFHPRGAPYKLALVNDRVLIPFRHSTSLAKSIHRAKIRADVPLRVSRGLGVEASPTLFDLPEPEAEPSLQDAAIAAHQANLTVVYVGFVANADADRVLEAWWGEAIALEDNGRIMWSPEKLPVDAVEPADYAQDDDPGALPGTGGAAADEGKPPVLRLVRGAGPAGA
>NZ_CP023445.1|WP_096496873.1|7211020_7213387_-|tetratricopeptide-repeat-protein
MTGEAGDFARNEFGGSADDVVQAGAVNGGVHFHGARPRAAWPPPRQLPADVRGYVNRNEELQRLNGFLNDHLGSDVSGVGLCVVTGTAGVGKTSLAVHWAHRVSAAFPDGQLYVNLRGYDPGPPVTPAHALDHFLRSLRDPGEPVPADLEGRAAAYRSMLAGRRVLVLLDNASDVAQVRPLLPGTAGCLVVITSRSRLSGLVARDGAHRLVLDVLTESQAVELLHGVTDNYRPPDDPAQLVELAGLCARLPLALRIAGERAGRRPHLPLRRLIEELRDESSLWDALTSDADEDGVRTVFAWSYRALTPDAGRLFRRLGLHTGAEFGAGAAAALVGADVRATRRLLDDLVGAHLVEQIGPDRFQFHDLLRAYATDQARVDETPESARAARRDLLLWYLRAAAAACALISPHTSRAALPQTPEGLGAEPPEFADQVEALRWLEVEHANLVVAVRHADQSGMPDLAWLLHVVLRPFHARSNRFDDWIETGDIALRAVRGLGDRAGEAEVLESLGKAHVQRGWAVEGAVRHRESLAIRRELGDRRGQMVSANALGLALLRDHRLSEALAAFEHARATAIELDDAHWTGLTTTNAAEVRCDLGDFEAGRDLLTEAAEVFRALDDRIWEAESLHGRSRAHRELGDLEAAQRDIRAALAVARDHDHPVAEAFWLIESGRVEVAAGRPERALVEYQRSAAMHRKVGDREREAVALDATGEAYARLGRVEDAERFHRGAVVVLRELGNRWQLAVALVNLAAVVDDPAETLAEAGALAAGFPDPEARALRERAARLAR
>NZ_CP023445.1|WP_096496874.1|7213383_7213977_-|hypothetical-protein
MSACTGVPLTLDEYVDGFERHHGVEGVGELWKIERTQVFQEEGNASCAAFLAGDRARSLALIAERLPQLEQQHRAATAHGMVVGRVRVVEEPLDPYVLWELTSQVQRAALGEQIKVVDAADLAGLEAGGPLPDLVGFDDAVVYFIHYTPDGVPTGATAATDHQVAHWRQVYRSLHDAAEPVADYHARRVAPELPEAP

Crispr_ID: NZ_CP023445_15

• CRISPR_ID: NZ_CP023445_15
• CRISPR_location: 7291985-7292092
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_15

Consensus_repeat	Method
ACCGCGCCGTCGCCGATCACCGCG	CRISPRCasFinder

spacers of NZ_CP023445_15

>15.1|7292009|60|NZ_CP023445|CRISPRCasFinder
TCGGCCACGACCGCGCCCGCCTGCACGAGCGCGCCCGCGCCGACGACGCTCCGCTCCACG

CRISPR arrays and Neighbor proteins around NZ_CP023445_15

CRISPR arrays

The CRISPR arrays of NZ_CP023445_15

>merge|NZ_CP023445|15|7291985-7292092|CRISPRCasFinder
ACCGCGCCGTCGCCGATCACCGCGTCGGCCACGACCGCGCCCGCCTGCACGAGCGCGCCCGCGCCGACGACGCTCCGCTCCACGACCGCGCCCTCGCCGATCACCGCG

>NZ_CP023445|15|13|7291985-7292092|CRISPRCasFinder
ACCGCGCCGTCGCCGATCACCGCG	TCGGCCACGACCGCGCCCGCCTGCACGAGCGCGCCCGCGCCGACGACGCTCCGCTCCACG
ACCGCGCCCTCGCCGATCACCGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_015805016.1|7286267_7286576_-|WhiB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376791
NZ_CP023445.1|WP_096496924.1|7288595_7289936_+|coenzyme-F420-0:L-glutamate-ligase	unknown	unknown	gnl|CDD|183957
NZ_CP023445.1|WP_157767917.1|7286833_7287583_+|site-2-protease-family-protein	unknown	unknown	gnl|CDD|100079
NZ_CP023445.1|WP_096496929.1|7293687_7294545_-|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|224137
NZ_CP023445.1|WP_096496932.1|7297592_7298495_+|glycosyltransferase	unknown	unknown	gnl|CDD|133029
NZ_CP023445.1|WP_096496928.1|7293122_7293512_+|hypothetical-protein	unknown	unknown	gnl|CDD|223062
NZ_CP023445.1|WP_096496933.1|7298511_7298895_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096498097.1|7278920_7280273_-|phosphomannomutase/phosphoglucomutase	unknown	unknown	gnl|CDD|236557
NZ_CP023445.1|WP_096496934.1|7299023_7301492_+|glycosyltransferase	unknown	unknown	gnl|CDD|133029
NZ_CP023445.1|WP_096496935.1|7301484_7302579_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340838
NZ_CP023445.1|WP_096496921.1|7282059_7286052_-|glycosyltransferase	unknown	unknown	gnl|CDD|224137
NZ_CP023445.1|WP_096496926.1|7290941_7291886_-|3-methyladenine-DNA-glycosylase	unknown	unknown	gnl|CDD|223200
NZ_CP023445.1|WP_096496930.1|7295075_7296209_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340838
NZ_CP023445.1|WP_096496923.1|7287607_7288573_+|2-phospho-L-lactate-transferase	unknown	unknown	gnl|CDD|237443
NZ_CP023445.1|WP_015805014.1|7280856_7281309_+|metallopeptidase-family-protein	unknown	unknown	gnl|CDD|240574
NZ_CP023445.1|WP_096496931.1|7296382_7297447_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340838
NZ_CP023445.1|WP_084799289.1|7280351_7280711_-|DUF3499-domain-containing-protein	unknown	unknown	gnl|CDD|378788
NZ_CP023445.1|WP_096496925.1|7289938_7290484_+|NUDIX-hydrolase	unknown	unknown	gnl|CDD|239646
NZ_CP023445.1|WP_096496937.1|7303862_7304855_-|dTDP-glucose-4,6-dehydratase	unknown	unknown	gnl|CDD|187557
NZ_CP023445.1|WP_096496936.1|7302972_7303863_-|dTDP-4-dehydrorhamnose-reductase	unknown	unknown	gnl|CDD|367904

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_015805016.1|7286267_7286576_-|WhiB-family-transcriptional-regulator	gnl|CDD|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	1.58795e-28
NZ_CP023445.1|WP_096496924.1|7288595_7289936_+|coenzyme-F420-0:L-glutamate-ligase	gnl|CDD|183957	PRK13294, PRK13294, F420-0--gamma-glutamyl ligase; Provisional.	0
NZ_CP023445.1|WP_157767917.1|7286833_7287583_+|site-2-protease-family-protein	gnl|CDD|100079	cd06158, S2P-M50_like_1, Uncharacterized homologs of Site-2 protease (S2P), zinc metalloproteases (MEROPS family M50) which cleave transmembrane domains of substrate proteins, regulating intramembrane proteolysis (RIP) of diverse signal transduction mechanisms. Members of the S2P/M50 family of RIP proteases use proteolytic activity within the membrane to transfer information across membranes to integrate gene expression with physiologic stresses occurring in another cellular compartment. In eukaryotic cells they regulate such processes as sterol and lipid metabolism, and endoplasmic reticulum stress responses. In prokaryotes they regulate such processes as sporulation, cell division, stress response, and cell differentiation. This group includes bacterial, eukaryotic, and Archaeal S2P/M50s homologs with a minimal core protein and no PDZ domains.	2.40244e-38
NZ_CP023445.1|WP_096496929.1|7293687_7294545_-|glycosyltransferase-family-2-protein	gnl|CDD|224137	COG1216, COG1216, Predicted glycosyltransferases [General function prediction only].	7.39215e-63
NZ_CP023445.1|WP_096496932.1|7297592_7298495_+|glycosyltransferase	gnl|CDD|133029	cd04186, GT_2_like_c, 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.	2.03242e-35
NZ_CP023445.1|WP_096496928.1|7293122_7293512_+|hypothetical-protein	gnl|CDD|223062	PHA03373, PHA03373, tegument protein; Provisional.	0.00520349
NZ_CP023445.1|WP_096498097.1|7278920_7280273_-|phosphomannomutase/phosphoglucomutase	gnl|CDD|236557	PRK09542, manB, phosphomannomutase/phosphoglucomutase; Reviewed.	0
NZ_CP023445.1|WP_096496934.1|7299023_7301492_+|glycosyltransferase	gnl|CDD|133029	cd04186, GT_2_like_c, 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.	6.63131e-55
NZ_CP023445.1|WP_096496935.1|7301484_7302579_+|glycosyltransferase-family-4-protein	gnl|CDD|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	2.75376e-75
NZ_CP023445.1|WP_096496921.1|7282059_7286052_-|glycosyltransferase	gnl|CDD|224137	COG1216, COG1216, Predicted glycosyltransferases [General function prediction only].	1.88252e-27
NZ_CP023445.1|WP_096496926.1|7290941_7291886_-|3-methyladenine-DNA-glycosylase	gnl|CDD|223200	COG0122, AlkA, 3-methyladenine DNA glycosylase/8-oxoguanine DNA glycosylase [DNA replication, recombination, and repair].	1.10888e-20
NZ_CP023445.1|WP_096496930.1|7295075_7296209_-|glycosyltransferase-family-4-protein	gnl|CDD|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	5.36188e-83
NZ_CP023445.1|WP_096496923.1|7287607_7288573_+|2-phospho-L-lactate-transferase	gnl|CDD|237443	PRK13606, PRK13606, LPPG:FO 2-phospho-L-lactate transferase; Provisional.	2.41688e-170
NZ_CP023445.1|WP_015805014.1|7280856_7281309_+|metallopeptidase-family-protein	gnl|CDD|240574	cd12954, MMP_TTHA0227_like_1, Minimal MMP-like domain found in a group of hypothetical proteins from alphaproteobacteria and actinobacteria. The subfamily includes some uncharacterized bacterial proteins which show high sequence similarity with Thermus thermophilus hypothetical protein TTHA0227. However, they do not contain the conserved HExxH (x could be any amino acid) motif. They may not have any zinc metallo-peptidase activity.	8.21732e-29
NZ_CP023445.1|WP_096496931.1|7296382_7297447_-|glycosyltransferase-family-4-protein	gnl|CDD|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	1.3431e-67
NZ_CP023445.1|WP_084799289.1|7280351_7280711_-|DUF3499-domain-containing-protein	gnl|CDD|378788	pfam12005, DUF3499, Protein of unknown function (DUF3499). This family of proteins is functionally uncharacterized. This protein is found in bacteria. Proteins in this family are typically between 125 to 163 amino acids in length.	4.52695e-59
NZ_CP023445.1|WP_096496925.1|7289938_7290484_+|NUDIX-hydrolase	gnl|CDD|239646	cd03674, Nudix_Hydrolase_1, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, U=I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	1.28587e-37
NZ_CP023445.1|WP_096496937.1|7303862_7304855_-|dTDP-glucose-4,6-dehydratase	gnl|CDD|187557	cd05246, dTDP_GD_SDR_e, dTDP-D-glucose 4,6-dehydratase, extended (e) SDRs. This subgroup contains dTDP-D-glucose 4,6-dehydratase and related proteins, members of the extended-SDR family, with the characteristic Rossmann fold core region, active site tetrad and NAD(P)-binding motif. dTDP-D-glucose 4,6-dehydratase is closely related to other sugar epimerases of the SDR family. dTDP-D-dlucose 4,6,-dehydratase catalyzes the second of four steps in the dTDP-L-rhamnose pathway (the dehydration of dTDP-D-glucose to dTDP-4-keto-6-deoxy-D-glucose) in the synthesis of L-rhamnose, a cell wall component of some pathogenic bacteria. In many gram negative bacteria, L-rhamnose is an important constituent of lipopoylsaccharide O-antigen. The larger N-terminal portion of dTDP-D-Glucose 4,6-dehydratase forms a Rossmann fold NAD-binding domain, while the C-terminus binds the sugar substrate. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	0
NZ_CP023445.1|WP_096496936.1|7302972_7303863_-|dTDP-4-dehydrorhamnose-reductase	gnl|CDD|367904	pfam04321, RmlD_sub_bind, RmlD substrate binding domain. L-rhamnose is a saccharide required for the virulence of some bacteria. Its precursor, dTDP-L-rhamnose, is synthesized by four different enzymes the final one of which is RmlD. The RmlD substrate binding domain is responsible for binding a sugar nucleotide.	2.15217e-110

Protein sequences

>NZ_CP023445.1|WP_096496926.1|7290941_7291886_-|3-methyladenine-DNA-glycosylase
MLGGVTAGAAPGESPLARSWSPPFPVDVGAVVAPVRRGPGDPSFHREAGGAVWLAAGTPRGAGTLRLAVAAGGVDARAWGPGAEWLLDGLPALLGADDDDSGFVAHHPLVAESRRRRPGVRLCSTRRVWDALLPAVLEQKVTGTEAQRSYRQLCVRFGERAPGPTPVPLHVPVGPRVVARLADWEWHAAGVDGARRRTLVAAAQVAHRLEAAAGIKGVLGRELLRKVPGIGVWTAAEVAQRAWGDADAVSFGDFHLAKTVGHALTGGPVDDDGMAGLLAPYAPQRHRAVVFLLLSGVRAPRRGVRFSARDHRRV
>NZ_CP023445.1|WP_096496925.1|7289938_7290484_+|NUDIX-hydrolase
MDGLRASALAVLGDWKPGTAEQEALRQAYLGFLLARPDACARACEPGHLTASAVVLDASGERVLLTLHPRVGRWLQLGGHCEETDATLPDAAMREATEESGIPGLVLDPEPVHLDVHPITCSLGKPTRHFDVRFVVRAPEGAVPVISAESKDLRWWPVDDLPENTEDLRPLIAAARARTKT
>NZ_CP023445.1|WP_096496924.1|7288595_7289936_+|coenzyme-F420-0:L-glutamate-ligase
MEPSGADHAASGGVTILPVPGLPEFRPGDDLAGALATAAPWLADGDVVVVTSKVVSKVEGRLVRVPADPEERDAVRRHWVRAEAVSVIARKNRTLITENKLGVIQAASGVDASNVAGDEIALLPVDPDASAAALRARLAELLGVAVAVVVTDTMGRAWRVGQTDAAIGAAGLAVLHRYAGSVDRQGNSLVVTEVAVADEIAAAADLVKGKLGAVPVAVVRGLPTTDDGSTARDLARPVEDDLFRMGTAEAIAKGRAEALLVRRSVRAFTDEPVDPALLRRAVGAALTAPAPHHTRPVRFVHVRERRTALLDAMRERWREDLRADGLSEEAVARRTARGDFLRDAPEIVLPFLIRSGAHAYPDERRAEAERTMFTIAGGAAVQGLLVALAAEGVGSCWVSSTIFCPDVVRAALDLPSSWEPLGAVAVGHPVEPLEARPLVEEGFVEL
>NZ_CP023445.1|WP_096496923.1|7287607_7288573_+|2-phospho-L-lactate-transferase
MKVVVVVGGVGGARFLVGLKSLLAGSEHEITAVVNTGDDVWMHGLRITPDLDTCMYTLGGGIDAERGWGRAGESWVVKEELAAYGADPEWFGLGDRDIATHLVRTRMLNAGYPLSAVVEALCHRWQPGVRLLPMSDDRVETHVVVEDDGGRRAIHFQEWWVKHRAKLPALSFASVGAEKARPAPGVLDAIAEADAVVLAPSNPVVSVGTVLAVPGIRDALRKTSAGVVGLSPIIGGKPLRGMADACLSAIGVETSAEAVGRLYGSRRMSEDGVLDAWLVHSGDRCDVPGVAVRAVPLLMSSPEATAEMARAALDLAGADVD
>NZ_CP023445.1|WP_157767917.1|7286833_7287583_+|site-2-protease-family-protein
MKSSAVRPSPLFLGLLAATVAGAVLTVLDSEIAITTGTVLLVLGGWAVSLCLHEFGHAMVAYKGGDFEVRDKGYLTLDIRRYTDPVLSLVLPLLLLAFGGIPLPGGAVWINHYALRSRRVESWVSLAGPLSNLVLGLLLALSVVLFSPPLALAAALSYLALLQVLAFTLNILPVPGLDGWGAIEPWLPPNVRAFGAKARPWAPLALFAVLIGLPALARPFFDLAYWVFGLVGGDAVLAYYGQSTFLFWR
>NZ_CP023445.1|WP_015805016.1|7286267_7286576_-|WhiB-family-transcriptional-regulator
MQEFDGGRVDGVDGQARELVVIGGSFDPADEQDWQERALCAQTDPEAFFPEKGGSTREAKRICLGCEVRSECLEYALAHDERFGIWGGLSERERRKLKKRAV
>NZ_CP023445.1|WP_096496921.1|7282059_7286052_-|glycosyltransferase
MTHGTPAPRTAPVLAVLVCHDGERWLGEALAALRAQRPAPRHVLAVDTGSRDGTAALLAAASAGVGGVPVAGAPSGVAPAAAAAVGVAGLLSGVLTLPRSTGFAEAVHAAVAHAEERWGDPGAWVWVLHDDSAPEPGCLSALLATAEIAPSSAVLGPLVVDWADPRVVVEAGLSTDASGRRQTGVGRGEPVGAFERTSEALAVGSAGALVRRSAWTGLGGYDRAFGLVGEDVDLGWRANLAGHSVLLVPAARLRHARALTTGERLLEPDGPGVGDGSEPPVGAGARGAVPARRRARSALRVTERTHGMRVLLINSGPTAFVLGLPRLTALSILRAAGLLLLRRLPDARAELTALHHLLTGRASLRAARAARPHRASLPGLLTSRTTRLRNTARATATHLVRRRVEADAALGKLPTPPTTAPPRAPEPEPEQQQQPEDLPRPVGPDALPAGALPRRRPVRTTGGLRKPATAVLLPIPNPATTLGSAPTLNAASTSGSSSALNAASAPDSAPALNAASAPGGAPAPNPASIPGPDPALTATSTPTPIPPLGTTPAPPTTSTPLPASAPTPAPGAARPSDTAPDAASAVSAAPPPDAASALVPLFVPALSSASVPPSTSVPPSASTPRPAPEAITPTPLRPSPVPRGTPLPPPLPRAVFVEVDRAAVLRSVLLGPPLLLALGLVLFALVANSGRLGLDLAGGRLLPVPALADLWSAYLSPWHPVSGGTTAPAPAALAVLGTAGALLGGPAAATALLLLGDAPLAGLAAYAATRRAPVPRPVRAFLAACYALLPASTAAVAQGRLDVVVVHVLLPPVLAGVAAVLRGGTGPAWLPVASGTALGLAALGAFSPLVHALVALAALIGFVAVPALVGDGRRRMAGLFAIVLLPMALLLPWPAVVVEHPVVLLHGVGAHQPTPPVSVTELLALTPGGDGALPWAGALLLPAALVAARLRPTRAMLPGAAAVVLAGFAAVALIAFPVTPMGGGDAHTGWTGAPLVLAGWGLVHVLLAACHRPTTAQPGLVAPPATRTGSPHAPRAGTPPVPHAEPPRAPRARLPKLLPATALVILLLVLVPAGVLGLRDGPLRADPVRLPSTLAAELPATNRSVLVLGEPTRQVAGRLPAFGDDDTPPTPSSPVRLARWTRDLTGGDQRRTRTALAQAAASGVSFVVPRDRAEADRMRAAAGDLLTTTPPLSDGRPVLRVLLTGGTALLLSPELARTARTGGDPPADQGTPGVVPVAADLPDAGARVSDGPAGRVLVLAAEEEPGWRATADGRPVPVLRAWGHLVAVPVPAQAADVRVEAPTLLRELLLLTQAAAVLVTLLTALPTRRR
>NZ_CP023445.1|WP_015805014.1|7280856_7281309_+|metallopeptidase-family-protein
MARGSRRQGPPRRRRRDRHGRGLRGPLYPATMPAARSRAERFDAVVLEALEPIEARWRTELTQLDVAVDDVPDVAPSTSGEDDDVVEDGNVPLARLMQPGQDRRARIVLYRRPLEARAKDGADLADLVHDVLVEQVANYLGLDPDVIDGE
>NZ_CP023445.1|WP_084799289.1|7280351_7280711_-|DUF3499-domain-containing-protein
MRSVRRCSRTGCANPAVATLTYAYADSTAVVGPLATSSEPHSYDLCEEHALRLTAPRGWEVVRYQGEFAPPEPTVDDLTALAEAVREAGRVDRSPQPPEVPLGTIRRGHLRVLPDPRED
>NZ_CP023445.1|WP_096498097.1|7278920_7280273_-|phosphomannomutase/phosphoglucomutase
MRDLSGIVKAYDIRGVVGEQLDVDVVRDFGAAFARLVGGPAIVIGHDMRDSSPGLAAAFAEGVTKQGVDVISIGLASTDMLYFASGKLDLPGAMFTASHNPAKYNGIKLCRAGAAPVGQDTGLTQIREDAEQGVADADGVAPGTLSERDMLTEYAAYLRELVDLRAIRPLKVVVDAGNGMGGHTVPVVFDGLPIDVVPMYFELDGNFPNHEANPLDPKNIVDLQAKVREVGADAGLAFDGDADRCFVVDERGEPVSPSAITALVASRELAKDPGGTIIHNLITSRAVPEIVRENGGTPVRTRVGHSFIKQEMATTGAIFGGEHSAHYYFRDFWRADTGMLAAMHVLAALGEQDGALSALTADYERYAASGEINSTVADQAGRLAAIKAEFGAREGVELDELDGLTVSLPDGSWFNLRASNTEPLLRLNVEAADAASVAALSDEVLAIVRA
>NZ_CP023445.1|WP_096496928.1|7293122_7293512_+|hypothetical-protein
MDPRARADAVLARARARGGVHIVTPNNMTSPMDSSSTQQIPRSVVEAAEPKGPDPDSTMILTTRIANGLQDVPPPPPAVKTPPPEPEERVAPGPVPTVQQVASRPSLSQRLSGGQGQQGGLAGRLNGEG
>NZ_CP023445.1|WP_096496929.1|7293687_7294545_-|glycosyltransferase-family-2-protein
MTRYGDDLAVVTVTYSPGDTLDRFLDTLAGATTRPVRVVLADNGSTDGVPERAAADRDDVEFVPTGGNLGYGGGANRGVAALDDSIGWIVIANPDLEWGEGSLDRLLDAATRWPRGGAFGPLVREPDGEVYPSARLLPSLGRGIGHALFAKVWPSNPWTREYRQERTGITERTAGWLSGSCLLLRREAFDSVDGFDARYFMYFEDVDLGDRMAKAGWLNVYVPTAEVVHIGGASTKKASGRMLAAHHSSAYRYLSDRHQGLVWAPMLLAVRLGLGLRLKLLTRRA
>NZ_CP023445.1|WP_096496930.1|7295075_7296209_-|glycosyltransferase-family-4-protein
MLIDATAVPADRGGVGRYVDSLVAALDADGAGVSVVCQPRDASHYRRLAPTSRVIAAAEAVATRTARLTWEQASLPRLVARLGVDVVHSPHYTLPLASRAASVVTLHDATFFTDPALHSSVKARFFRAWTRASLRRASLCVVPSHATADELARVAGADRTALHIAQHGVDTERFHPPTPQQVASVRASLGLGATPYVAFLGALEPRKNVPALIRGFARACQGRANPPALVLAGQPGWDGQVERALDSVPHRIRVIRAGYLPFDDLAGFLGGAELVAYPSLGEGFGLPVLEAMACGAAVLTTRRLSLPEVGGDAVAYCGVGAGDIAAALTSLLDDPSRRHALSTAALVRAKDFSWETSAARHRLAYARAAHAHQATKR
>NZ_CP023445.1|WP_096496931.1|7296382_7297447_-|glycosyltransferase-family-4-protein
MPNLVVLAEQLLAPVPGGTGRYTRELTAALAATAPPGWTVTTAVSRHPDPSAAAVPGVGAPRVLPIPRRALIAAWERGVPYWPGGDAVHAPTPLAPPRGRVVVTVHDTVPWTHPETLTPRGAAWHRRVIARAAARPTPLVVPTLAVADDLRTRVPCAAPPIAIPHGVTPLGESSPLADVPDRYVLAIGTIEPRKGLEALVAATARLGVPLLVVGQRGWGEVDLSAPHVRLLGKLPDPQLAHVLRGATALAVPSLAEGFGLPLVEAMSEGVPVVHSDAPALVEVAGGAGLVAERGDPRSLEAALRSVLTDRPLAARLAAAGRRRAEDFTWERAARAVWELHLAQAATASAERGAR
>NZ_CP023445.1|WP_096496932.1|7297592_7298495_+|glycosyltransferase
MVVVTWRGREHVTDCLDALSAQRRAHRLLVVDNASDDGTAGLLAAHPSRPEVVRLPRNAGYAGALAAVLPRVGTEFVAWLNDDAAPEPTWLAALEDELRRDRGAAAATSSMLLPDGSTQSVGVRITADGHGADLVLAGRDVFGFCGGAALVRTAELVGAGGVPGSFFCYYEDTDTSWRLRLSGHRVVSVGPARVRHRHGASSEPGSPLFHRWNERNRLLMLLRCAPAGVALRELARFAAITALLPVRGGRPEGANFRVGLRLRVIGEVLLRLPSALVQRAAIGRRAKVSRADVWREWAGR
>NZ_CP023445.1|WP_096496933.1|7298511_7298895_+|hypothetical-protein
MAEYVEVRTEDGDLVPFEIDEEHDGPVRVGRRWDRTKELAEDTLEGGVELARSVAGTVAQRIGSLRSPAPDRVAVEIGLKVGASGLFAIARSTAEAHVKITVEWQRESLATVEAERDEDGEEPGGGD
>NZ_CP023445.1|WP_096496934.1|7299023_7301492_+|glycosyltransferase
MTVVVVNYRGAEDTTTCLRALFTDVDYPPDLLQVVCVDNASGDGSAELIRTSVPRAEVVEAPENLGFAGGCNLGARRAKGSVLAFLNNDARPDAGWLREAVRVLREDPAVGAVASKVLDWDGKVVDFVDAGLTWFGMGYKRHAGEVDDGSHDAPRDVLFATGSAMVVRTELFAELRGFDERFFMFYEDVDLGWRLNLRGWRVRYEPKSLTFHKHHASMKSVDTSRELFLLERNALAALYKNLSDDVLAKVLPAALALVVRRATARGDIDPTQLEITRRPADPADDAAPVPIARQALAGFLAIDQFVELLPSLAESRKAEQAARRRTDADLLPLMRKAMEPAYPLPRYLAAHEVLVDVFGLEGVFGRPRRVLVLTGDAISPKMAGPAIRAWNMADVLVAEHDVRLVTVNPLCAPPDAPFPVLRARQKELGEHVDWADVVVLQGHALEYLPQVKERSSTKVVVCDMYDPMHLELLEQGKDGTDEQRALDLVGVTRVLNTQLARGDFFLCASERQRHFWLGHLAALGRLTPSLYDTDPTVRSLLAVAPFGLSAKPPTRTGPGLRDALGIGADDKVVLWAGGVYSWFDPLTLVSAVDELRERRPDARLVFLGMKHPNPEVPDMDVAGQTRALAGRLGLTNKHVFFNESWVAYQDRQNWLLDADCGVTTHYEHVETTFAFRTRVLDYLWAGLPIVTTDGDSFADLVEREGLGVVVPSEDPMALAAALEKAMYDEEFAAACAERIAVVRERFTWEVALAPLVEFCRNPRPSADRLPGSSPMVRNKPLGTREKVERDIKLVREYLDAGGPSELAKRATGRVLKKLRGRG
>NZ_CP023445.1|WP_096496935.1|7301484_7302579_+|glycosyltransferase-family-4-protein
MARRPLTVLLDGTPLLGQRTGIGRYTAALAEELASMVDEVDVRAVAFTLRGWRALRTVLPHDVVARGLPVSARLLRQFWLRAPFPPVEVLAGLADVMHATNFVLPPSVRAGGVVTIHDLAMLDHPGDLPPSDARLPELVRQSASRAAVVCTPTRAVADQVVERLGVPEDRIVVTPLGVDPAWFAARPPSDPVRARLRLPLEYLLFVGAGGPRKGLDRLIAAHAARPELPPLVLAGPGESGVDGRVVRTGYLTEIDLRRVVAGASALVLPSRDEGFGLPVLEALACNVPVVCSDVPALREVAGGHAVHVPVGDVEALGQALVETVETPPSPTAQAARRAHASEFTWRRTAELTVKAYEKAAKRRR
>NZ_CP023445.1|WP_096496936.1|7302972_7303863_-|dTDP-4-dehydrorhamnose-reductase
MAATALLVPGGRGQLGQDLLATGGRVRALSSAELDITDADAVADRVAEFAAGARAEGLAPVVVNAAAYTAVDNAETDEGRALAVNALGPELLALACREHDVPLLHVSTDYVFPGDATAPYEPDDATGPRSAYGRTKLAGEQRALAAWDRTWVVRTAWVYGAGGSNFVKTVARLAGQRESLSVVDDQRGSPTWSADLAAGLVELAAATTGPAAPAQRVLHATGGGETTWFGFARAVFEELGLDPERVRPCGTEDFPRPAPRPAYSVLSPKAWESAGLTPLRPWREALAVAVREGVAG
>NZ_CP023445.1|WP_096496937.1|7303862_7304855_-|dTDP-glucose-4,6-dehydratase
MRVLVTGGAGFIGSHYVRELVGGAYPAYADAEVVVLDKLTYAGNEANLAPVADSPRLRFVQGDICDRDLVAELVKGADAVVHFAAESHVDRSISGSADFVLTNVLGTQTMLQAALEAEVSRFVHVSTDEVYGSIERGSWTEDHVLEPNSPYSASKASSDLLARAFHRTHGLPVCVTRCSNNYGPYQFPEKVIPLFVTNLVDGKKVPLYGDGLNVRDWLHVDDHCRGIQLVLEGGRGGEIYNIGGGTELTNRELTEKLLEATGRDWDDSVEPVTDRKGHDRRYSVDITKINQELGYSPRVDFAEGLASTVAWYRDNRDWWEPLKQRASLAR

Crispr_ID: NZ_CP023445_16

• CRISPR_ID: NZ_CP023445_16
• CRISPR_location: 7637194-7637891
• CRISPR_type: Orphan
• Repeat_type: I-C,I-E,II-B
• Spacer_info: 11 spacers

Consensus repeat of NZ_CP023445_16

Consensus_repeat	Method
GGAACACCCCCGCGTGCGCGGGGAAGAC	CRISPRCasFinder
GGAACACCCCCGCGTGCGCGGGGAAGACN	CRT
GTCTTCCCCGCGCACGCGGGGGTGTTCC	PILER-CR

spacers of NZ_CP023445_16

>16.1|7637222|33|NZ_CP023445|CRISPRCasFinder
GATAGCGCGATCTACCGCAACGACCGCGGCTAC
>16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT
GGCCGGGTCGACGCGGACGCGGACGTACTCGCC
>16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT
TTCATGCGCGCCCTGAAGCGGGTCGCGGTCTAC
>16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
GATCTGGCGGTCCCGGCCAGCGGGTTCGCCCTG
>16.5|7637466|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
TACCCGTCCACACCACGCGTGACCTGGTCGTAG
>16.6|7637527|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
AGCCCAGGAGGGCCCGTGATCACGAGCACCAGG
>16.7|7637588|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
GCGGTCATCGCCTCGTCGAGGTCCAACCCGCCC
>16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
GGCGTGAAGAACCTGAACGCGGCGGGCGTCGAG
>16.9|7637710|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
GGCCTCCCGCCGGTCTCCATCAGCGCGATCCGC
>16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
CCACCATCCACGCGGACCAGCTCGGCCTGCAC
>16.11|7637831|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR
TTGAACAGGACCCCGGACACCCGATCCACCCCA
>16.12|7637223|32|NZ_CP023445|CRT
ATAGCGCGATCTACCGCAACGACCGCGGCTAC

CRISPR arrays and Neighbor proteins around NZ_CP023445_16

CRISPR arrays

The CRISPR arrays of NZ_CP023445_16

>merge|NZ_CP023445|16|7637194-7637891|CRISPRCasFinder,CRT,PILER-CR
CGGAACACCCCACGTGCACGGGGAAGACGATAGCGCGATCTACCGCAACGACCGCGGCTACGGAACACCCCCGCGTGCGCAGGGAAGACGGCCGGGTCGACGCGGACGCGGACGTACTCGCCGGAACACCCCCGCATACGCGGGAAAGACTTCATGCGCGCCCTGAAGCGGGTCGCGGTCTACGGAACACCCCCGCGTGCGCGGGGAAGACGATCTGGCGGTCCCGGCCAGCGGGTTCGCCCTGGGAACACCCCCGCGTGCACGGGGAAGACTACCCGTCCACACCACGCGTGACCTGGTCGTAGGGAACACCCCCGCGTACGCGGGGAAGACAGCCCAGGAGGGCCCGTGATCACGAGCACCAGGGGAACACCCCCGCGTGCGCGGGGAAGACGCGGTCATCGCCTCGTCGAGGTCCAACCCGCCCGGAACACCCCCGCGTGCGCGGGGAAGACGGCGTGAAGAACCTGAACGCGGCGGGCGTCGAGGGAACACCCCCGCGTGCGCGGGGAAGACGGCCTCCCGCCGGTCTCCATCAGCGCGATCCGCGGAACACCCCCGCGTGCGCGGGGAAGACCCACCATCCACGCGGACCAGCTCGGCCTGCACGGAACACCCCCGCGTGCGCGGGGAAGACTTGAACAGGACCCCGGACACCCGATCCACCCCAGGAACACCCCCGCGTGCGCGGGGAAGAC

>NZ_CP023445|16|14|7637194-7637891|CRISPRCasFinder
CGGAACACCCCACGTGCACGGGGAAGAC	GATAGCGCGATCTACCGCAACGACCGCGGCTAC
GGAACACCCCCGCGTGCGCAGGGAAGAC	GGCCGGGTCGACGCGGACGCGGACGTACTCGCC
GGAACACCCCCGCATACGCGGGAAAGAC	TTCATGCGCGCCCTGAAGCGGGTCGCGGTCTAC
GGAACACCCCCGCGTGCGCGGGGAAGAC	GATCTGGCGGTCCCGGCCAGCGGGTTCGCCCTG
GGAACACCCCCGCGTGCACGGGGAAGAC	TACCCGTCCACACCACGCGTGACCTGGTCGTAG
GGAACACCCCCGCGTACGCGGGGAAGAC	AGCCCAGGAGGGCCCGTGATCACGAGCACCAGG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GCGGTCATCGCCTCGTCGAGGTCCAACCCGCCC
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCGTGAAGAACCTGAACGCGGCGGGCGTCGAG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCCTCCCGCCGGTCTCCATCAGCGCGATCCGC
GGAACACCCCCGCGTGCGCGGGGAAGAC	CCACCATCCACGCGGACCAGCTCGGCCTGCAC
GGAACACCCCCGCGTGCGCGGGGAAGAC	TTGAACAGGACCCCGGACACCCGATCCACCCCA
GGAACACCCCCGCGTGCGCGGGGAAGAC

>NZ_CP023445|16|4|7637195-7637891|CRT
GGAACACCCCACGTGCACGGGGAAGACG	ATAGCGCGATCTACCGCAACGACCGCGGCTAC
GGAACACCCCCGCGTGCGCAGGGAAGAC	GGCCGGGTCGACGCGGACGCGGACGTACTCGCC
GGAACACCCCCGCATACGCGGGAAAGAC	TTCATGCGCGCCCTGAAGCGGGTCGCGGTCTAC
GGAACACCCCCGCGTGCGCGGGGAAGAC	GATCTGGCGGTCCCGGCCAGCGGGTTCGCCCTG
GGAACACCCCCGCGTGCACGGGGAAGAC	TACCCGTCCACACCACGCGTGACCTGGTCGTAG
GGAACACCCCCGCGTACGCGGGGAAGAC	AGCCCAGGAGGGCCCGTGATCACGAGCACCAGG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GCGGTCATCGCCTCGTCGAGGTCCAACCCGCCC
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCGTGAAGAACCTGAACGCGGCGGGCGTCGAG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCCTCCCGCCGGTCTCCATCAGCGCGATCCGC
GGAACACCCCCGCGTGCGCGGGGAAGAC	CCACCATCCACGCGGACCAGCTCGGCCTGCAC
GGAACACCCCCGCGTGCGCGGGGAAGAC	TTGAACAGGACCCCGGACACCCGATCCACCCCA
GGAACACCCCCGCGTGCGCGGGGAAGAC

>NZ_CP023445|16|2|7637377-7637891|PILER-CR
GGAACACCCCCGCGTGCGCGGGGAAGAC	GATCTGGCGGTCCCGGCCAGCGGGTTCGCCCTG
GGAACACCCCCGCGTGCACGGGGAAGAC	TACCCGTCCACACCACGCGTGACCTGGTCGTAG
GGAACACCCCCGCGTACGCGGGGAAGAC	AGCCCAGGAGGGCCCGTGATCACGAGCACCAGG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GCGGTCATCGCCTCGTCGAGGTCCAACCCGCCC
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCGTGAAGAACCTGAACGCGGCGGGCGTCGAG
GGAACACCCCCGCGTGCGCGGGGAAGAC	GGCCTCCCGCCGGTCTCCATCAGCGCGATCCGC
GGAACACCCCCGCGTGCGCGGGGAAGAC	CCACCATCCACGCGGACCAGCTCGGCCTGCAC
GGAACACCCCCGCGTGCGCGGGGAAGAC	TTGAACAGGACCCCGGACACCCGATCCACCCCA
GGAACACCCCCGCGTGCGCGGGGAAGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096497156.1|7638023_7638998_+|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl|CDD|366736
NZ_CP023445.1|WP_096492573.1|7642806_7643142_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_015805323.1|7630389_7630554_-|50S-ribosomal-protein-L33	unknown	unknown	gnl|CDD|234783
NZ_CP023445.1|WP_096497155.1|7635800_7636070_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497150.1|7628266_7628878_+|DUF4190-domain-containing-protein	unknown	unknown	gnl|CDD|379388
NZ_CP023445.1|WP_096497159.1|7640984_7641245_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497151.1|7628990_7629389_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_015805321.1|7629453_7629873_-|MaoC-family-dehydratase	unknown	unknown	gnl|CDD|239537
NZ_CP023445.1|WP_157767939.1|7640497_7640884_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|153418
NZ_CP023445.1|WP_096497153.1|7631133_7633749_-|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|238923
NZ_CP023445.1|WP_015805325.1|7635007_7635529_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_157767940.1|7643407_7644763_+|hypothetical-protein	unknown	unknown	gnl|CDD|369506
NZ_CP023445.1|WP_157767576.1|7643141_7643408_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497154.1|7633989_7634865_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497714.1|7641289_7641544_+|WhiB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376791
NZ_CP023445.1|WP_096497157.1|7638957_7640358_-|regulator	unknown	unknown	unknown
NZ_CP023445.1|WP_096492574.1|7642528_7642708_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497149.1|7626784_7628026_+|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl|CDD|235596
NZ_CP023445.1|WP_096492575.1|7641543_7642098_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497152.1|7629869_7630316_-|MaoC-family-dehydratase	unknown	unknown	gnl|CDD|379194

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096497153.1|7631133_7633749_-|EAL-domain-containing-protein	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.	1.86796e-99
NZ_CP023445.1|WP_096497156.1|7638023_7638998_+|aminoglycoside-phosphotransferase-family-protein	gnl|CDD|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	2.47757e-13
NZ_CP023445.1|WP_157767939.1|7640497_7640884_-|GntR-family-transcriptional-regulator	gnl|CDD|153418	cd07377, WHTH_GntR, Winged helix-turn-helix (WHTH) DNA-binding domain of the GntR family of transcriptional regulators. This CD represents the winged HTH DNA-binding domain of the GntR (named after the gluconate operon repressor in Bacillus subtilis) family of bacterial transcriptional regulators and their putative homologs found in eukaryota and archaea. The GntR family has over 6000 members distributed among almost all bacterial species, which is comprised of FadR, HutC, MocR, YtrA, AraR, PlmA, and other subfamilies for the regulation of the most varied biological process. The monomeric proteins of the GntR family are characterized by two function domains: a small highly conserved winged helix-turn-helix prokaryotic DNA binding domain in the N-terminus, and a very diverse regulatory ligand-binding domain in the C-terminus for effector-binding/oligomerization, which provides the basis for the subfamily classifications. Binding of the effector to GntR-like transcriptional regulators is presumed to result in a conformational change that regulates the DNA-binding affinity of the repressor. The GntR-like proteins bind as dimers, where each monomer recognizes a half-site of 2-fold symmetric DNA sequences.	7.62687e-16
NZ_CP023445.1|WP_015805323.1|7630389_7630554_-|50S-ribosomal-protein-L33	gnl|CDD|234783	PRK00504, rpmG, 50S ribosomal protein L33; Validated.	1.0384e-20
NZ_CP023445.1|WP_157767940.1|7643407_7644763_+|hypothetical-protein	gnl|CDD|369506	pfam07767, Nop53, Nop53 (60S ribosomal biogenesis). This nucleolar family of proteins are involved in 60S ribosomal biogenesis. They are specifically involved in the processing beyond the 27S stage of 25S rRNA maturation. This family contains sequences that bear similarity to the glioma tumor suppressor candidate region gene 2 protein (p60). This protein has been found to interact with herpes simplex type 1 regulatory proteins.	0.00385131
NZ_CP023445.1|WP_096497150.1|7628266_7628878_+|DUF4190-domain-containing-protein	gnl|CDD|379388	pfam13828, DUF4190, Domain of unknown function (DUF4190). This integral membrane domain is functionally uncharacterized. One of the membrane helices contains two GXXG motifs that are usually associated with dimerization.	2.90619e-09
NZ_CP023445.1|WP_096497714.1|7641289_7641544_+|WhiB-family-transcriptional-regulator	gnl|CDD|376791	pfam02467, Whib, Transcription factor WhiB. WhiB is a putative transcription factor in Actinobacteria, required for differentiation and sporulation.	1.19198e-25
NZ_CP023445.1|WP_096497149.1|7626784_7628026_+|pyridoxal-phosphate-dependent-aminotransferase	gnl|CDD|235596	PRK05764, PRK05764, aspartate aminotransferase; Provisional.	0
NZ_CP023445.1|WP_015805321.1|7629453_7629873_-|MaoC-family-dehydratase	gnl|CDD|239537	cd03453, SAV4209_like, SAV4209_like. Similar in sequence to the Streptomyces avermitilis SAV4209 protein, with a hot dog fold that is similar to those of (R)-specific enoyl-CoA hydratase, the peroxisomal Hydratase-Dehydrogenase-Epimerase (HDE) protein, and the fatty acid synthase beta subunit.	1.62104e-50
NZ_CP023445.1|WP_096497152.1|7629869_7630316_-|MaoC-family-dehydratase	gnl|CDD|379194	pfam13452, MaoC_dehydrat_N, N-terminal half of MaoC dehydratase. It is clear from the structures of bacterial members of MaoC dehydratase, pfam01575, that the full-length functional dehydratase enzyme is made up of two structures that dimerize to form a whole. Divergence of the N- and C- monomers in higher eukaryotes has led to two distinct domains, this one and MaoC_dehydratas. However, in order to function as an enzyme both are required together.	2.08805e-33

Protein sequences

>NZ_CP023445.1|WP_096497155.1|7635800_7636070_+|hypothetical-protein
MIETTIELSGRVRAMLRAVAAGRAELSGGGEPDLYVDGLPCSDRAAIHDLVHLGLVRALAAVRLDERAVAELTEAGRAAIAQGSNMCSR
>NZ_CP023445.1|WP_015805325.1|7635007_7635529_-|hypothetical-protein
MTGTWIVIAGVVVGVVIGLALRPPGARREPATRQPPPRERLVALLAAADELERGLDAVLDFGPLSAGELAAVDLPAKLEHLVAPRVLTCPTVAELRACTEQIALHPFPEQRELLAAVRADQRPAAMSATWLVMREAAGSAAAQHHAAVEARRCLATIRDQLTPELPGPTPALV
>NZ_CP023445.1|WP_096497154.1|7633989_7634865_+|hypothetical-protein
MRRSALERGGRPALRSGADPLLPDLAPVDRPYSLQEHSPEELGATWRAPRSHVLAWSPGDDPGRRLREWPLTGGGDPETAALVTVPSRAEDAPRVLLAHGFAPLVVLAVRVAGRATPPGDAAVEVRPLRGEDLDVAAALHLEVVRVDARYGVVTERASTGRLLRELLAGEVGRAEPEAWPAWRGGEPVGLLTCQGPAGSGWVAGRTSVSPVAYLGALGGAGGPARGRGRRGAGGVAARAAGRAAGRGGRRRAPAAPLPAEPALDAVLVLAGVPAAVDDVAAAARSVRRAAR
>NZ_CP023445.1|WP_096497153.1|7631133_7633749_-|EAL-domain-containing-protein
MSDQTSAPTSNTSPRSTNRAFTAFAVLLLAAGVLSAFLVGANLPDDPSRLSLLWTGPLLVVGFLLAEQLAINVDVRSGVAWTISFTEIPLVLGLLVAPFEVVLAAHVVAGVGTLLGRRVLDRAVYNAGLMFMEISVAFAVADAVNRFVGDSGPAWAGAFVGTISVPLLASVLGLTALRLMRKGMRLAPSGRLVLQTLVVALLNTAAGLVAYEVADHAQWGGLLIVLAFAGITAIYLAYSGLLREQRDLEALSEVSLRVARSGRHGTGPRGGATTAVDAEDGKAEADEWQHIAERIREQLNANRVVLRLRTDPQAPMRTLVAGEPLPQAMRRDDARLSREDAMLQLPGTQVRYFRVADAGEEATDALVRRDAQEALVVPLRGGATQLLGAVEVHDRLSRWRGFGKADIQLLRTLANHLSTAVDNRRLLARLRHDAYHDPLTGLLNRTGFLEAAAEPVRESEAAVVLRVDLDVLSTVLDALGQAWGNRMVVAAGRRLRDELGPEVPLARLDGGAFAALLVDRKAERVKEIAERLRARLSVPYPVDRLTVEAGAIVGWAAVAEVEDDAKDADSLLQRADVALRATSENEPMRAYAPSMGQIFLRRFQLVTQFRSALENGQISVHYQPKIALPSRQVIGAESLVRWKHPEFGRVDPDEFIPAVEATGLVDVLTDFVMDKGLERVRRWMDRDLRMSIAVNLSVRTLADEEFPDRVKEALDRHRVPPELLTFELTESGVMADPERALPVLRRLHTMGVVLAVDDFGTGYSSLAYLRQLPVDEVKIDKSFVLGMGTDLGDMAVVRSIVELGHSLGLTVVAEGVEDDAARDQLVGMGCDVAQGYLISRPLSEDRFEAWLRARTVQVRGARDETVLTLVH
>NZ_CP023445.1|WP_015805323.1|7630389_7630554_-|50S-ribosomal-protein-L33
MAATDVRPKITLACEECKHRNYITRKNRRNDPDRLEIKKFCPNCKTHKAHKETR
>NZ_CP023445.1|WP_096497152.1|7629869_7630316_-|MaoC-family-dehydratase
MPLDASFIGRSYPPTPPYEVGREKIREFADAVGATSAVHRDADAARAAGHPDVIAPPTFAILVSMSANSQLVEDPELGLDYTRVVHGDQAFSHHRPIVAGDVLSVALTVDNITSRMGNDMLSLRAEITDQHGAAVTTARSTLVVRGES
>NZ_CP023445.1|WP_015805321.1|7629453_7629873_-|MaoC-family-dehydratase
MITAAEVSVGDELPPITLRITRAHLVAYAGASLDFNPIHWNQRFAEGVGLPGVIAHGMLTMGMACRIVTEWAGDPAAVVEYGTRFGRPVPVPDDDEGAVVEVTAKVTKVLEDGTFKVNINASHDGKSVLGGASARVRLP
>NZ_CP023445.1|WP_096497151.1|7628990_7629389_+|hypothetical-protein
MGSAREVERSRRWLVVSAASLLLLGALVGAVLVNGPSAPRSATVVYEVTGEAGHATVVYSTFDDGGVSTGQEELSSLPWRREVTAPGDARGVLTVTIGEQGGEVGCQVSVDGVERRSASASGPGSSAFCGGF
>NZ_CP023445.1|WP_096497150.1|7628266_7628878_+|DUF4190-domain-containing-protein
MSYPQQPTQYAPQGHPQPAQNGMATGSLVLGLVGLLLSFIPFIGVIAWPMVIVGLVLGLVAISKLKKNPANSKGLAISGTILSALGLIVCILWAAVFGAAVNEVDEQSKKEVTVVYEVTGEAPSVSVSYSTFGDGNMQNSSEDVTTLPWTKELKTTGLFSGGSLTVSTGAEGGSVTCKVTVDGQEQKTSTASGPFAVASCSGF
>NZ_CP023445.1|WP_096497149.1|7626784_7628026_+|pyridoxal-phosphate-dependent-aminotransferase
MAEPETTPAPTAPALPRISRRIGGIAESATLAVDAKAKALKAAGRPVIGFGAGEPDFPTPEAVVAAAQAACADPRNHRYTPAAGLPELREAVAAKTRRDSGYEVAASQVLITNGGKQAVYQAFATIVDPGDEVLLPAPYWTTYPEAITLAGGVPVQVTADETTDYLVTVEQLEAARTPRTKVLLLCSPSNPTGSVYSREAITAIGRWAHANGLWVISDEIYEHLVYDGAEAVSLPVAVPEMADRTIVLNGVAKTYAMTGWRVGWLIGPADVVKAASNLQSHLSSNVSNVAQRAALEAVSGSLEAAHAMRVAFDRRRRLIVELLSAIPGVDCPTPTGAFYVYPSVKALIGKELRGQEITDSVTLAALILEHAEVAVVPGEAFGTPGYLRLSYALGDEDLKTGLDRMAKLLAEVK
>NZ_CP023445.1|WP_096497156.1|7638023_7638998_+|aminoglycoside-phosphotransferase-family-protein
MVSTTTSRALLSDRQKPFRSTSSVQAVTPSRSTSPLTSAEAERVLITACRQVDLDPADAELLRIGSNAVYRLRTPVIVRIAQADADEAGARRQVAVARWLAAVDYPATRALRVKQPVKTDGGLVTFWESASEREDYAPIIQVARLIRELHELPPPRLNLPAFEPFTQTLTDIEQHTGKENLDFLKEPLEKLKAEYALLTFPLPAGVIHGDANVGNVILDRDGNPLLIDLDNFAIGPREWDLVQTAAFYERFGWHTEAEYRTFVNVYGFDIMEWPGYRVLADYREIAMTVWLARKAAGNPEAGAELTKRLAALRTGGSRADWEPL
>NZ_CP023445.1|WP_096497157.1|7638957_7640358_-|regulator
MYGNERLAALMREAGFLREDGSVGRKTFARAVSTHAGRPLTHTYVSRWLDGMVPRDLPTRRAIATALGQRLGRTVGLEELGFGRTEKLPADLGLKYPDSSQEGIAALTRLWQGDLDQVHTLLASPTNVAAWNEASLSWLVSSAADVELLSTGARVVGLADLARVRTTVDLFDRLDAQFGGGHARRSLVEFLRNDLAQLLRGTYTDVVGRELFQVAASATMLGAWMSYDAGLHGLAQRYFVQALKLADAAGDRLLAAGILDAMSHQATFLGRYREAANLARAARVGTESAGSARSAAHFSAMEARALARLGDTAACDRAMAVAVREFERCEGDDQAEWFGYFDDAELAAELGHCNRDLGRAVDATTYAMQSVGGNGEQVRSDFFATMVLADAYLHQGEAEEACRVALTALQVGEQLVSARCASYVGEFRQRLDGLGDSPVARAFVEQARTTRLWATAVPSPRGSRRS
>NZ_CP023445.1|WP_157767939.1|7640497_7640884_-|GntR-family-transcriptional-regulator
MADDVENAAEQRSRAQLADEIRRDIDAGRYPVGDRLPGYRELGRRMGAAPNTVGEAVRQLAAEGRVRIKANAGAFVCEVDDEPLTAEQQIREARADLLDLRDKLRSVRRELDALDDKVGDLIDRLPSS
>NZ_CP023445.1|WP_096497159.1|7640984_7641245_+|hypothetical-protein
MNEPYLVIQPKQQANEPAPRPTTTTTLPKSDLELLSSALQDALTAQKQGLVIGPPVDEITLRRAERRARRADAARTQETYIVGGAA
>NZ_CP023445.1|WP_096497714.1|7641289_7641544_+|WhiB-family-transcriptional-regulator
MGSLSGTDFGAHPACVGEDPELFFPFPGQHDQVAAAKSVCGRCPVRQACLAHALHHDAEGVWGGTTEDERRQLRVVVVDREAVA
>NZ_CP023445.1|WP_096492575.1|7641543_7642098_+|hypothetical-protein
MASAFRVDDGGDRSAASDGVSRFGVYLERSGFERVEDAASFATSVVRVALPPVMSPGYVWQHPRVQDVSALRGDAGELVFAVSLVSALPAALEPMGRRSLGWERKRSAGQVSWLEPERWDRVALLPSLVVRVPVPVEALPAPRYRADGVPELGASKRAVRVVVAELERVVAPVLAVLEPHGAVA
>NZ_CP023445.1|WP_096492574.1|7642528_7642708_+|hypothetical-protein
MSKHQRNLIDPTTGNRFTQDRPYGPVQPVTSSDGTPPPSQRSRSWEHLVASGYDLQPDD
>NZ_CP023445.1|WP_096492573.1|7642806_7643142_+|hypothetical-protein
MSSTDKSHKPLLRPDEYREAARTVLTLTDADQDLLARAAGRYLDVADVVERAAEVPAERRAQFAHDVDHVVEHLVKALTVTTNNSWPLLATARVYLRLAGDAARPQQGWVA
>NZ_CP023445.1|WP_157767576.1|7643141_7643408_+|hypothetical-protein
MAMGCLGRMLSAPFVLVGSLLKLLFLPALVLVFVVLLAPEGWGLVVGVGLAGYLAGVITAFRAGARGMTRSLERSGIRFTGDERAGRR
>NZ_CP023445.1|WP_157767940.1|7643407_7644763_+|hypothetical-protein
MAVIDRRAVRIAADAEAKIRVADAEAARKLEAQRARIELERLQAEADRVSRAERDVERRAERERRRDERRVRRAEGKARRAELVAGVLDGFADKVIVVPVLMAMAGAWWGQFQVFHQRLSWPVPLAAAAATGIECIGVVCGRLAHLARRQVTVTGADGVQVTRDDSAWVERSVMWAVVGYAAASNWAHAGDPTVGALSVVGVAVWEARERRVHRLALAEAGRLPARRPRFGAVRWVRYPGWTWRAWSAALRHGLADAAEALAVADRETAERKVRRASHRALGWRARRRFGRVVAKRLEATDVARRAAAAEVIRQAEEVIGAAAMLFGPRALTEATRSRPTSANTVPAEDDGKVSRSRRWGRNLQASASPEHAAEATGTAAGDTGESALVVVDGVDITDLMPTARTVAAGLGDRLNRDGLLDGLREAGLSVGGRRRKAVYDAVLAERDRVAA

Crispr_ID: NZ_CP023445_17

• CRISPR_ID: NZ_CP023445_17
• CRISPR_location: 7961288-7961390
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP023445_17

Consensus_repeat	Method
GGTCAGGCCTGCGAGGCGGTCAG	CRISPRCasFinder

spacers of NZ_CP023445_17

>17.1|7961311|57|NZ_CP023445|CRISPRCasFinder
CCCGTGAGGGTCAGGCCTGCGAGGCGGTCAGCCCGCGAAGTGGTCAGCCCGTGAGGC

CRISPR arrays and Neighbor proteins around NZ_CP023445_17

CRISPR arrays

The CRISPR arrays of NZ_CP023445_17

>merge|NZ_CP023445|17|7961288-7961390|CRISPRCasFinder
TGATCAGCCTGCGGGGCGGTCAGCCCGTGAGGGTCAGGCCTGCGAGGCGGTCAGCCCGCGAAGTGGTCAGCCCGTGAGGCGGTTAGGCCTGCGAGGCGGTCAG

>NZ_CP023445|17|15|7961288-7961390|CRISPRCasFinder
TGATCAGCCTGCGGGGCGGTCAG	CCCGTGAGGGTCAGGCCTGCGAGGCGGTCAGCCCGCGAAGTGGTCAGCCCGTGAGGC
GGTTAGGCCTGCGAGGCGGTCAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023445.1|WP_096497403.1|7954212_7954992_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|223377
NZ_CP023445.1|WP_096497415.1|7970371_7970752_-|phage-holin-family-protein	unknown	unknown	gnl|CDD|377198
NZ_CP023445.1|WP_096497405.1|7955821_7958404_-|ATP-dependent-chaperone-ClpB	unknown	unknown	gnl|CDD|274529
NZ_CP023445.1|WP_096497409.1|7963121_7963778_-|nucleotide-exchange-factor-GrpE	unknown	unknown	gnl|CDD|237632
NZ_CP023445.1|WP_096497413.1|7967532_7967862_-|multidrug-efflux-SMR-transporter	unknown	unknown	gnl|CDD|224987
NZ_CP023445.1|WP_096497398.1|7951133_7951688_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP023445.1|WP_096497416.1|7970786_7971980_-|hypothetical-protein	unknown	unknown	gnl|CDD|375050
NZ_CP023445.1|WP_157767961.1|7951754_7952309_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497402.1|7953656_7954010_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497404.1|7954988_7955693_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497406.1|7958916_7959300_+|glyoxalase	unknown	unknown	gnl|CDD|380093
NZ_CP023445.1|WP_096497411.1|7965844_7966651_-|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|371327
NZ_CP023445.1|WP_096497401.1|7952742_7953660_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497408.1|7961910_7963101_-|molecular-chaperone-DnaJ	unknown	unknown	gnl|CDD|237655
NZ_CP023445.1|WP_096497412.1|7966795_7967371_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497414.1|7968019_7970296_+|(Fe-S)-binding-protein	unknown	unknown	gnl|CDD|223325
NZ_CP023445.1|WP_096497400.1|7952341_7952746_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP023445.1|WP_096497410.1|7963774_7965631_-|molecular-chaperone-DnaK	unknown	unknown	gnl|CDD|234715
NZ_CP023445.1|WP_015805617.1|7959766_7960870_+|flavohemoprotein	unknown	unknown	gnl|CDD|99784
NZ_CP023445.1|WP_096497407.1|7961482_7961914_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|133394

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP023445.1|WP_096497403.1|7954212_7954992_-|SDR-family-oxidoreductase	gnl|CDD|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	3.13828e-84
NZ_CP023445.1|WP_096497416.1|7970786_7971980_-|hypothetical-protein	gnl|CDD|375050	pfam17210, SdrD_B, SdrD B-like domain. This family corresponds to the B-like domain from the SdrD protein. This domain has three calcium binding sites within a greek key beta sandwich fold.	9.34599e-06
NZ_CP023445.1|WP_096497405.1|7955821_7958404_-|ATP-dependent-chaperone-ClpB	gnl|CDD|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP023445.1|WP_096497409.1|7963121_7963778_-|nucleotide-exchange-factor-GrpE	gnl|CDD|237632	PRK14164, PRK14164, heat shock protein GrpE; Provisional.	6.738e-45
NZ_CP023445.1|WP_096497413.1|7967532_7967862_-|multidrug-efflux-SMR-transporter	gnl|CDD|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	1.7929e-21
NZ_CP023445.1|WP_096497398.1|7951133_7951688_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	9.8832e-60
NZ_CP023445.1|WP_096497410.1|7963774_7965631_-|molecular-chaperone-DnaK	gnl|CDD|234715	PRK00290, dnaK, molecular chaperone DnaK; Provisional.	0
NZ_CP023445.1|WP_096497415.1|7970371_7970752_-|phage-holin-family-protein	gnl|CDD|377198	pfam04020, Phage_holin_4_2, Mycobacterial 4 TMS phage holin, superfamily IV. These proteins are predicted transmembrane proteins with probably four transmembrane spans. The 1.E.40 is represented by the mycobacterial 4 phage holin, but it also contains many cyanobacterial. proteobacterial and firmicute proteins. Holins are encoded within the genomes of Gram-positive and Gram-negative bacteria as well as in those of the bacteriophage of these organisms. The primary function of holins appears to be transport of murein hydrolases across the cytoplasmic membrane to the cell wall where these enzymes hydrolyze the cell wall polymer as a prelude to cell lysis. When chromosomally encoded the enzymes are therefore autolysins. Holins may also facilitate leakage of electrolytes and nutrients from the cell cytoplasm, thereby promoting cell death. Some may catalyze export of nucleases.	1.78448e-18
NZ_CP023445.1|WP_096497406.1|7958916_7959300_+|glyoxalase	gnl|CDD|380093	pfam18029, Glyoxalase_6, Glyoxalase-like domain. This entry comprises a diverse set of domains related to the Glyoxalase domain. The exact specificity of these proteins is uncertain.	1.64903e-29
NZ_CP023445.1|WP_096497411.1|7965844_7966651_-|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|371327	pfam10988, DUF2807, Putative auto-transporter adhesin, head GIN domain. This bacterial family of proteins shows structural similarity to other pectin lyase families. Although structures from this family align with acetyl-transferases, there is no conservation of catalytic residues found. It is likely that the function is one of cell-adhesion. In Structure 3jx8, it is interesting to note that the sequence of contains several well defined sequence repeats, centred around GSG motifs defining the tight beta turn between the two sheets of the super-helix; there are 8 such repeats in the C-terminal half of the protein, which could be grouped into 4 repeats of two. It seems likely that this family belongs to the superfamily of trimeric auto-transporter adhesins (TAAs), which are important virulence factors in Gram-negative pathogens. In the case of Parabacteroides distasonis, which is a component of the normal distal human gut microbiota, TAA-like complexes probably modulate adherence to the host (information derived from TOPSAN).	0.00759992
NZ_CP023445.1|WP_096497408.1|7961910_7963101_-|molecular-chaperone-DnaJ	gnl|CDD|237655	PRK14279, PRK14279, molecular chaperone DnaJ.	0
NZ_CP023445.1|WP_096497414.1|7968019_7970296_+|(Fe-S)-binding-protein	gnl|CDD|223325	COG0247, GlpC, Fe-S oxidoreductase [Energy production and conversion].	3.69942e-84
NZ_CP023445.1|WP_015805617.1|7959766_7960870_+|flavohemoprotein	gnl|CDD|99784	cd06187, O2ase_reductase_like, The oxygenase reductase FAD/NADH binding domain acts as part of the multi-component bacterial oxygenases which oxidize hydrocarbons using oxygen as the oxidant. Electron transfer is from NADH via FAD (in the oxygenase reductase) and an [2FE-2S] ferredoxin center (fused to the FAD/NADH domain and/or discrete) to the oxygenase. Dioxygenases add both atoms of oxygen to the substrate, while mono-oxygenases (aka mixed oxygenases) add one atom to the substrate and one atom to water. In dioxygenases, Class I enzymes are 2 component, containing a reductase with Rieske type [2Fe-2S] redox centers and an oxygenase. Class II are 3 component, having discrete flavin and ferredoxin proteins and an oxygenase. Class III have 2 [2Fe-2S] centers, one fused to the flavin domain and the other separate.	7.14023e-100
NZ_CP023445.1|WP_096497407.1|7961482_7961914_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|133394	cd04766, HTH_HspR, Helix-Turn-Helix DNA binding domain of the HspR transcription regulator. Helix-turn-helix (HTH) transcription regulator HspR, N-terminal domain. Heat shock protein regulators (HspR) have been shown to regulate expression of specific regulons in response to high temperature or high osmolarity in Streptomyces and Helicobacter, respectively. These proteins share the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their conserved N-terminal domains contain predicted winged HTH motifs that mediate DNA binding, while the dissimilar C-terminal domains bind specific coactivator molecules.	1.13615e-38

Protein sequences

>NZ_CP023445.1|WP_015805617.1|7959766_7960870_+|flavohemoprotein
MVRLIRESFAVVESRSDDVAKFFYGMLFSLAPATREMFPANMEVQRSRLLRALVHVVQMVDRPDDLIPFLRQLGRDHRKFGVVSSHYESVGTALLAAIKKYAGEAWTPQVEMAWAEAYTIMARAMQEAAHADEGPAYWHATVLEHQRVSWDLAVVRLQPDHPVNYRAGQYVSVETPQRARLWRYFSPANAPREDGIIEFHIRSVEGGWVSRSIVGHTQPGDVWRIGPPMGRLSVNRTSGNNVLMIAGGTGIAPMHAMLDEMAQWGENPKTHLFIGGRTREDLYDLDNLQRMASANPWLSIVPVLENDPGARGVEQGTLADVVTRYGAWEDRDVLVCGSPSMIRATVSRMLVAGTPLDRIKYDPFTLD
>NZ_CP023445.1|WP_096497406.1|7958916_7959300_+|glyoxalase
MASLVRHLTFDCADPWALATFWTGITGGALGEGDQPGDDEVEVVWDGGVNLLFIRVPEGKSAKNRLHLDLQPHDRTRDEEVERVVAFGATVLDDQRNADGTGWVVLADPEGNEFCVVRSTAERVSHP
>NZ_CP023445.1|WP_096497405.1|7955821_7958404_-|ATP-dependent-chaperone-ClpB
MDAFNPTTKSQQAVSAAVQAATIAGNPDVGPVHLLGALLAQGEGLAAPLLSGVGADPGVIRKELEQLSRSLPAASGSSVSAPQFSRDAVRVLTRAQELATEMGDEYVSTEHLLVGLAQHGGQVADLLRRHGANPEALREAFEKVRGSARVTSPDPEGTYKALEKYGVDLTARARRGELDPVIGRDSEIRRVVQVLSRRTKNNPVLIGEPGVGKTAIVEGLAQRVVAGDVPESLRGKRVVSLDLGSMVAGAKYRGEFEERLKAVLKEITDSAGQVITFIDELHTIVGAGATGESAMDAGNMIKPMLARGELRLVGATTLDEYRSHVEKDPALERRFQQVLVGEPSVEDTIGILRGLKERYEVHHGVRITDAALVAASTLSDRYITARFLPDKAIDLVDEAASRLRMEIDSRPVEIDEVERAVRRLEIEEMALAKESDEASRERLAALRAELAERRESLAALTARWQNEKGSIDKVRVLKEQLEQLRGESERAERDGDLGKASELRYGRIPVLEKDLEEATRTTQEAAVMLKEEVGPDDVADVVSAWTGIPAGRMLEGETTKLLRMEDELTGRVVGQAEAVRVVSDAVRRTRAGVADPDRPTGSFLFLGPTGVGKTELAKALAQFLFDDERAMIRIDMSEYSEKHSVARLVGAPPGYVGYDQGGQLTESVRRRPYSVVLLDEVEKAHPDVFDVLLQVLDDGRLTDGQGRTVDFRNTILVLTSNLGSHAIADVSLDERGRKDAVMQVVRGHFKPEFLNRLDDVVVFRALATEELTSIVDIQVAKLAARLAQRRLALEVTPAAREWLALNGFDPVYGARPLRRLVQSAIGDQLARELLSGEVRDGDAVRVDVLDDATGLIVGRA
>NZ_CP023445.1|WP_096497404.1|7954988_7955693_-|hypothetical-protein
MGIPAWVWFTVAAVAGIAGFALIATDRAQRTARNRERRRWAALRGWQFEETDQVLTSRWESGAIAYYGTGTAKDVVAGSTFTADGRRQVYVLDHETNNKVNSVLVGVRCRRSLPVVVELWLHSVPFQRDQMPDLLGPVGSRYAFVSEVPAARKLITPDLVDAAEEIGADVTVVWLEGDWVMAAAPPNSTPSRIERLLRDLGELADVVDPFDAEPDDESGSGSGEVIRPSFGRKQ
>NZ_CP023445.1|WP_096497403.1|7954212_7954992_-|SDR-family-oxidoreductase
MSAPTALVTGASAGIGAAFARRLAAEGHDLVLVARTAERLEALAQELRARHGVEVTAFPADLSTAEGRLAVEELLAGSEVDLLVNNAGFTNSAEFFQAEADQLEAQLDVNVTSVLRLTRAALPGMVARRSGAVVNVSSVAGFLPGRGSSYSADKAWVTTFSEGMAQSTEGTGVRVMALCPGFTRTEFHERAGIDMTKTPDLLYLDADRVVHEALADLRAGKQVSIPSPQYKAIITGARLLPRAVLRKIASRVLGGRGRT
>NZ_CP023445.1|WP_096497402.1|7953656_7954010_-|hypothetical-protein
MGERFHVEPDELSGYSELLTRNAGHFLTIREHAVSKGGDTSGFTGLLALLRPAVTGVAELYGETLEFANSMMTKEAAALDEAAESYRAVDAHAQALLRQVQQALEAAAEAPAVGGGE
>NZ_CP023445.1|WP_096497401.1|7952742_7953660_-|hypothetical-protein
MTAYADVENPATALAAAPEDRPGRQSTKELIEKAGWKIQGVNWIYEQVTGENLIESLINPLLGDFEKIDANAAAWDRVAKSLDAVRHNVDAGAGQLGPHWDGDAAQSFEARMRTLWVVAIEADSQVARIVGNQFQSTASACRTATGLALTLLDMLVGKLIEAAMTAWIPVVGWGRAVWMVYDAVQIVDAIRKIIISIQTLIEGVQGMVNGLKGMGTALMKLKDVRDVGDALDVLDAYQDGQQKFGDGLSAAKSGAIGVAMNSYKLGSSVNKANTRYTAPPPGASPPPPPPPAQSGAPSSGGGGGE
>NZ_CP023445.1|WP_096497400.1|7952341_7952746_-|hypothetical-protein
MTFPYDRAKLDALVADVEARNAALIKTATEASRVRTTSRGLSDADLAQISRAANNPRAPQALRDLAKRVDAGELSWKDIAEGKALDDEGVRRAMATGIPDLKRAHNAIREGQDVQDLARGGDGDEPGSFTEDAW
>NZ_CP023445.1|WP_157767961.1|7951754_7952309_+|hypothetical-protein
MTLPDVLLVEHPWSFTDHLLKVRYSVRVYAESDAPLAHTEDLGGLGPLVALRRTAFSGRTAFRVALSTPGGPLLEVRKGWGAPPTEVLLPGGRALGSLRKEGGGGVGLHDASGVRLCALGDVAGMSYRQLAKRDGARVRRDVLRLRVGLAEPVRSLAIAAGVFYDVVRGVGVNHASGGPIDSPF
>NZ_CP023445.1|WP_096497398.1|7951133_7951688_-|orotate-phosphoribosyltransferase
MVLDAVAKAELARLVSELAVVHGKVTLSSGAEADYYIDLRRATLHHAAAPLIGKLLRQLTADWDYAASGGLTLGADPVACAIMHSAAADGEVLDAFVVRKAAKQHGMQRRIEGVDVEGKRVLAVEDTSTTGGSVMTAVEALREAGAIVVGVVTVVDRGTGAREVIEAEGLSYRYLLDLADLGLA
>NZ_CP023445.1|WP_096497407.1|7961482_7961914_-|helix-turn-helix-transcriptional-regulator
MTFPFPPGTDEDTPFFVISVAAQLSGLHAQTLRSYDRMGLVSPGRTTGGGRRYSMRDIVLLREVQRLSQEDGVNLAGIKRIIDLENEVGALRGKVAELTEQLSNAMAAAEAAAATVHASYRRDLVPVRHETALVVWKPQQRRR
>NZ_CP023445.1|WP_096497408.1|7961910_7963101_-|molecular-chaperone-DnaJ
MSARDWIEKDFYRELGVSSDASAEEIKKSYRKLARELHPDANPGDAKAEARFKAVSEAYGVLSDSAKRKQYDEARRLFAGGGGFPGGFGGGGGGGFDVGDLFGRGAAGAQGGMGGGGLGDLLGGLFNRRGGGAATGANRPRRGEDVETDVRIDFTEAVKGATVPLRLSSPAACATCSGSGAKPGTTPRTCGNCGGAGLVTRSQGAFAFSEPCQDCRGTGRIVDDPCQECGGDGVSTRTRTLTIRIPSGVDDGQRIRLANQGEPGRNGGPTGDLFVRVHVNPHPIFGRSGNDVTLTVPVTFPELALGTSLTVPTLEGKVTVKVPAGTNSGRVMRAKGKGIARRDGKVGDLLITLQVAVPNNTDAKSRDALEAYAKTTSQHDPRAELNALLLERGKST
>NZ_CP023445.1|WP_096497409.1|7963121_7963778_-|nucleotide-exchange-factor-GrpE
MTSADQQQPEDVSAEEQPDVRRIDPETGEIRAESAAESTSPAGNGGGKHAAPEPEGAAEVDPAAELKAQLDERTADLQRLTAEYANYRKRVERDREVVVATAKAKVVGDLLGVLDDVERAGQHGDLTGAFKAVADKLVAALTATGLEGFGEAGEAFDPAVHEAVQHSTSPDVAGPTVTAVFRRGYRFADRVLRPAMVVVTDYEPAPAQPEQAQAEQQD
>NZ_CP023445.1|WP_096497410.1|7963774_7965631_-|molecular-chaperone-DnaK
MARAVGIDLGTTNSVVAVLEGGEPTVIANSEGSRTTPSIVAFAKNGEVLTGQPAKNQAVTNVDRTIRSVKRHIGTTWTTDEVDGKKYTPQEISARVLMKLKRDAEAYLGEEITDAVITVPAYFEDSQRQATKEAGQIAGLNVLRIVNEPTSAALAYGLDKGEKEQTILVFDLGGGTFDVSLLELGDGVVEVRATSGDNHLGGDDWDQRVVDWLVERFKQANGIDLTKDKMALQRIREAAEKAKIELSSSNSASINLPYITVDSDKNPLFLDETLSRAEFQRITNDLLERTRAPFTNVIKDAGISVGDIDHVVLVGGSTRMPAVSELVKELTGGREPNKGVNPDEVVAVGAALQAGVLRGEVKDVLLLDVTPLSLGIETKGGVMTKLIERNTTIPTKRSEIFTTADDNQPSVQIQVFQGERDFAADNKKLGMFELTGLPPAPRGVPQIEVTFDIDANGIVHVSAKDMGTGKEQRMTITGGSALPKDDIEQMIKDAEAHAEEDKRRRDEAEVRNQAETLVYQTEKVVKENEDKIPAEVQEKVRAAIAETSEALKGTDIAKVRAAVEKLATESQAIGQAMYAGAAPTDAAAGSAPGAEGAKPGAKADDVVDAEIVDEDEKK
>NZ_CP023445.1|WP_096497411.1|7965844_7966651_-|DUF4097-family-beta-strand-repeat-protein
MGSEGRARGARRSFAVALAVVLVAGTASCVRLVWKEATDRYGLGRPVTEVRLAQSDGDVVFRHRPGAEAVLTRSLRYSRHEAKTPATSHRVDGETLVLEGCGLHCTATYDLVLPDLVRITGESDGGDVSAEGALSVDLEVDSGNVVLNQTAEGVSLRGNSSDVSLSGAGGPLDVRLDSGNLRATGMTGGPVTVTTGSGRVELGLVAPASVRARTDGGALTVRVPAGAYKVVTETDSGEVDITGVVDDKAAPYELFLRTDSGNMVIGRV
>NZ_CP023445.1|WP_096497412.1|7966795_7967371_-|hypothetical-protein
MGFTGRESWQVSHGSNHTVTTALFVRDTLALSVDTVPELPGLDPAVPVVVPRGVDRAGAAQEWLGWWADVLDHARADRHGTSPAAPDSRSLAQRPALRGAVRALQDLVGDYHHRRSRRGRHAALPVGEVVRGVETRLGRPVRPFRLVITVVPVQGLVWERMTGSHVIASEWFLDDPGRSAPALRAIVEDLA
>NZ_CP023445.1|WP_096497413.1|7967532_7967862_-|multidrug-efflux-SMR-transporter
MVHLLLALAIVAEVTATVSLKLSAGFTKLAPSVVVVIAYAIAFGALSQVLKLGMPLGVAYAIWCAFGIAAVAAVGVVLFGERVNATMVVGLLLVIAGVVAIELGSSSGS
>NZ_CP023445.1|WP_096497414.1|7968019_7970296_+|(Fe-S)-binding-protein
MGALQLTLGAIGVAASAYAWGIFVAGVVRMVRIIRLGQPDATRNGPVWPRLRTLVVEFVAHTRMAKLRKVAPWHWMVMWGFLIGSAVLFEAYGEVFYPGFHWPVIGTWSAWALLIELLGIGTVVGGVALAVIRQLNHPRRADRVSRFAGSDFKAAYFVEAVVIVEGLGILGVKAFKQASGLEDPPLWSSFVTAPLSELLPASPDWVSVMAFVKLVTALVWLAVVAKNLTMGVAWHRFSAFFNIYFKREDDGGVALGALRPMMSGGKVLDLEEADPDTDVFGVGKVEDFTWKGWLDFSTCTECGRCQSQCPAWNTGKPLSPKLMITELRDHAYAKAPYLLAGGRRDMAGDEVGLVEDKYEDYKKRLESIDVLAMAEAERPLVGEAGELGVIDPEVLWSCTTCGACVEQCPVDIEHVDHIVDMRRYQVLIESNFPSELGGMFKNLENKGNPWGQNAKDRLAWADDLDFEVPVFDGELGDAEYLFWVGCAGAFEDRAKKTTRAVAELLHTAGVKYTVLGPEESCTGDPARRAGNEFLFQMLAQQNVEVLNSVFEGREPGRRKVVVTCAHCFNTLANEYPQVGGQYEVVHHTQLLNRLVRERRLVPVAEIAEDVTYHDPCYIGRHNKIYEAPRELIGASGAKLREMPRNSDKAMCCGAGGARMWMEERIGKRINLDRVDEALGTAPSKIATGCPFCRVMLTDGVTARQNEKVVGGGVEVVDVAQLLLTAVRRGQERERADVPTDESSTGTPLPDGDKAAASD
>NZ_CP023445.1|WP_096497415.1|7970371_7970752_-|phage-holin-family-protein
MGIVAQVLLTAVAVWVSTLIPGIDLEGGSTPAKIGTLVAVAVVFGLVNAVVKPVVKFLGCLFYLLTLGLIGLVVNALMFWLTGWVAGELGLPFQVTGFWPAFFGAIIVALASWLLNLVYERAVEQD
>NZ_CP023445.1|WP_096497416.1|7970786_7971980_-|hypothetical-protein
MKKLVAVTAVLMLLGGGTALAQDGEVLDGLIWFDRNGNGVVDAGEPALASGKGVRVFNAATKEHIGDYGTDANGRYRATGLPAGVPLAIYNANTDRYATTTPSSVFRTGGATLDFGIRGGVVTGSAFVDADRDGVRDAGERELQPAHRLGGLTATGSYRVEDVPEGDHELVLADLRAQGLLPSAVTAELFVGKGEQVRLDTPYFAPRADLVLGALKLGPDKPGARATGDEVELSFAITNSGEAADGVRFTVDRPKAKLLSTGEGVVAEGDGFALTAPLEPGATATARLRYALTDPTITGFRVVLAPGTSFGDGDPSDNTAEVALSVTAPPSSTPPSTTSTAPGSSTAPTTTAPPVGGAPKQLARTGAAPFWPLVTGLALLVAGLALHHAARTRRRRA

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP023445_13	13.5|6969581|22|NZ_CP023445|CRISPRCasFinder	6969581-6969602	22	NZ_CP021374	Rhizobium sp. ACO-34A plasmid pRACO34Ab, complete sequence	239000-239021	1	0.955
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MG593802	Streptomyces phage Omar, complete genome	22071-22097	2	0.926
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MH509442	Mycobacterium phage Aminay, complete genome	23016-23042	2	0.926
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_JX627580	Methylobacterium oryzae CBMB20 plasmid pMOC1, complete sequence	109152-109178	3	0.889
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MN204498	Streptomyces phage Saftant, complete genome	22971-22997	3	0.889
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	KY676784	Streptomyces phage ToastyFinz, complete genome	5511-5540	3	0.9
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_AP022607	Mycobacterium branderi strain JCM 12687 plasmid pJCM12687	346902-346928	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_023600	Mycobacterium phage Jolie1, complete genome	22628-22654	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_022061	Mycobacterium phage KayaCho, complete genome	22616-22642	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KJ433975	Mycobacterium phage 40BC, complete genome	22636-22662	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KJ433973	Mycobacterium phage 39HC, complete genome	22636-22662	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_024145	Mycobacterium phage Hosp, complete genome	20832-20858	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	914077-914103	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP018471	Xanthomonas vesicatoria strain LM159 plasmid pLM159.2, complete sequence	50082-50108	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_KJ588780	Achromobacter xylosoxidans strain A22732 plasmid pA22732-IMP, complete sequence	28692-28718	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_KP289281	Pseudomonas sp. EGD-AKN5 plasmid unnamed, complete sequence	16924-16950	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_MN366359	Bacterium plasmid pALTS31, complete sequence	26285-26311	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_001735	Enterobacter aerogenes plasmid R751, complete sequence	46630-46656	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP015373	Pandoraea pnomenusa strain MCB032 plasmid unnamed 2, complete sequence	37823-37849	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	AGRM01000006	Salmonella enterica subsp. houtenae str. ATCC BAA-1581 plasmid pSEHO0A1, complete sequence, whole genome shotgun sequence	21472-21498	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_017908	Mycobacterium abscessus subsp. bolletii F1725 plasmid BRA100, complete sequence	26407-26433	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	AJ863570	Uncultured bacterium IncP-1beta multiresistance plasmid pB8	41224-41250	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_008459	Bordetella pertussis plasmid pBP136 DNA, complete sequence	34512-34538	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KU238092	Uncultured bacterium plasmid pDTC28, complete sequence	25403-25429	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JX469834	Uncultured bacterium plasmid pDS3, complete sequence	24032-24058	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JX469831	Uncultured bacterium plasmid pKSP212, complete sequence	30874-30900	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106172	Uncultured bacterium plasmid pAKD29, complete sequence	23871-23897	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106173	Uncultured bacterium plasmid pAKD31, complete sequence	25049-25075	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106174	Uncultured bacterium plasmid pAKD33, complete sequence	25052-25078	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_004956	Pseudomonas sp. ADP atrazine catabolic plasmid pADP-1, complete sequence	16924-16950	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106164	Uncultured bacterium plasmid pAKD1, complete sequence	37199-37225	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106165	Uncultured bacterium plasmid pAKD14, complete sequence	25049-25075	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106166	Uncultured bacterium plasmid pAKD15, complete sequence	25049-25075	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106168	Uncultured bacterium plasmid pAKD17, complete sequence	25049-25075	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JN106169	Uncultured bacterium plasmid pAKD18, complete sequence	25034-25060	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_014911	Alicycliphilus denitrificans BC plasmid pALIDE02, complete sequence	7617-7643	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MN386974	Pseudomonas aeruginosa strain 1943 plasmid pPaeBURNS1, complete sequence	33226-33252	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MG879028	Uncultured bacterium plasmid pEG1-1, complete sequence	57257-57283	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP021650	Acidovorax sp. T1 plasmid p2-T1, complete sequence	7354-7380	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KF743817	Proteus mirabilis plasmid R772, complete sequence	23964-23990	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KF743818	Bordetella bronchiseptica plasmid R906, complete sequence	26182-26208	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JX486125	Uncultured bacterium plasmid pRWC72a, complete sequence	35759-35785	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP019238	Rhodoferax koreense strain DCY-110 plasmid unnamed2	41678-41704	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP038640	Cupriavidus oxalaticus strain X32 plasmid unnamed5, complete sequence	59404-59430	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KC170279	Uncultured bacterium plasmid pMBUI8, complete sequence	36018-36044	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KU356987	Variovorax paradoxus plasmid pBS64, complete sequence	41449-41475	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	KU356988	Variovorax paradoxus plasmid pHB44, complete sequence	40154-40180	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP009797	Burkholderia ambifaria AMMD plasmid pBII_1, complete sequence	26789-26815	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_013176	Pseudomonas putida plasmid pW2, complete sequence	20166-20192	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_019312	Delftia sp. KV29 plasmid pKV29, complete sequence	26422-26448	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_019320	Variovorax sp. DB1 plasmid pDB1, complete sequence	58478-58504	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP017455	Dickeya solani strain PPO 9019 plasmid unnamed, complete sequence	33880-33906	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_021077	Comamonas sp. 7D-2 plasmid pBHB, complete sequence	95372-95398	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_007337	Cupriavidus pinatubonensis JMP134 plasmid 1, complete sequence	80897-80923	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_024998	Acidovorax avenae subsp. avenae plasmid pAAA83 DNA, complete sequence, strain: 83	14354-14380	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_MH053445	Pseudomonas aeruginosa strain PA1280 plasmid pICP-4GES, complete sequence	25567-25593	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_005088	Delftia acidovorans B plasmid pUO1, complete sequence	51679-51705	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_008385	Burkholderia ambifaria AMMD plasmid unnamed1, complete sequence	19646-19672	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MH669016	Streptomyces phage TrvxScott, complete genome	21787-21813	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MT711979	Streptomyces phage Endor2, complete genome	22830-22856	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MK524524	Streptomyces phage Caelum, complete genome	21774-21800	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MK392365	Streptomyces phage TinaBelcher, complete genome	21756-21782	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MH651190	Streptomyces phage Thestral, complete genome	21809-21835	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	872420-872446	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_LR134456	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence	69820-69846	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1467165-1467191	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP025614	Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed2, complete sequence	57890-57916	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1688616-1688642	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	877099-877125	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	1756352-1756378	4	0.852
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1255285-1255311	4	0.852
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NZ_CP035092	Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence	525465-525489	4	0.84
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NC_008688	Paracoccus denitrificans PD1222 plasmid 1, complete sequence	118998-119022	4	0.84
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NC_017966	Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence	292807-292831	4	0.84
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NZ_CP010683	Phaeobacter piscinae strain P14 plasmid pP14_b, complete sequence	14558-14582	4	0.84
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NZ_CP010718	Phaeobacter piscinae strain P18 plasmid pP18_c, complete sequence	14558-14582	4	0.84
NZ_CP023445_3	3.1|1316611|25|NZ_CP023445|CRISPRCasFinder	1316611-1316635	25	NZ_CP010859	Marinovum algicola DG 898 plasmid pMaD4, complete sequence	79078-79102	4	0.84
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP049751	Rhodococcus fascians A21d2 plasmid unnamed2, complete sequence	38744-38770	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	LR134127	Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7	112013-112039	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP009803	Streptomyces sp. FR-008 plasmid pSSFR1, complete sequence	96301-96327	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP009803	Streptomyces sp. FR-008 plasmid pSSFR1, complete sequence	97394-97420	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1770010-1770036	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1751429-1751455	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP022220	Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence	723845-723871	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	249368-249394	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_AP021877	Desulfosarcina ovata strain 28bB2T plasmid Do28_1, complete sequence	32535-32561	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP030052	Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence	336684-336710	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP030054	Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence	516277-516303	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP041045	Paracoccus sp. AK26 plasmid pAK1, complete sequence	469790-469816	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_015721	Bdellovibrio phage phi1402, complete genome	7768-7794	5	0.815
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	JF344709	Bdellovibrio phage phi1402, complete sequence	7768-7794	5	0.815
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP033195	Xanthomonas oryzae pv. oryzae strain CIAT plasmid unnamed, complete sequence	68836-68865	5	0.833
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP022994	Paraburkholderia aromaticivorans strain BN5 plasmid pBN4, complete sequence	14137-14166	5	0.833
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP026110	Paraburkholderia hospita strain DSM 17164 plasmid pEMT1, complete sequence	96266-96295	5	0.833
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	CP000620	Burkholderia vietnamiensis G4 plasmid pBVIE04, complete sequence	24302-24331	5	0.833
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP033202	Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence	27955-27984	5	0.833
NZ_CP023445_16	16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT	7637283-7637315	33	NZ_LR134450	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 8, complete sequence	102081-102113	5	0.848
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	255425-255457	6	0.818
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	795916-795948	6	0.818
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	960467-960499	6	0.818
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1194185-1194217	6	0.818
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	453171-453203	6	0.818
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	7368-7400	6	0.818
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	665031-665057	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	1552031-1552057	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP045122	Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence	90061-90087	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3539519-3539545	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NZ_CP025547	Mycobacterium paragordonae strain 49061 plasmid unnamed1, complete sequence	261645-261671	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_007950	Polaromonas sp. JS666 plasmid 2, complete sequence	198266-198292	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	MN908689	Arthrobacter phage DrSierra, complete genome	25082-25108	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	LR743530	Xanthomonas phage Suba genome assembly, chromosome: 1	28402-28428	6	0.778
NZ_CP023445_1	1.4|30352|27|NZ_CP023445|CRT	30352-30378	27	NC_049432	Ralstonia phage RsoM1USA, complete genome	10897-10923	6	0.778
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	255425-255457	6	0.818
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	795916-795948	6	0.818
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NC_016585	Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence	960467-960499	6	0.818
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1194185-1194217	6	0.818
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	453171-453203	6	0.818
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP026305	Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence	7368-7400	6	0.818
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	NZ_CP011274	Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence	21731-21765	6	0.829
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NZ_AP022607	Mycobacterium branderi strain JCM 12687 plasmid pJCM12687	90152-90184	6	0.818
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	857353-857382	6	0.8
NZ_CP023445_16	16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT	7637283-7637315	33	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	160666-160698	6	0.818
NZ_CP023445_16	16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT	7637344-7637376	33	NZ_CP051543	Paracoccus sanguinis strain OM2164 plasmid pPspOM122, complete sequence	77435-77467	6	0.818
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	874334-874365	6	0.812
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP015291	Rhodobacter sphaeroides strain MBTLJ-20 plasmid c, complete sequence	44704-44736	7	0.788
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP047040	Rhodobacter sphaeroides strain 2.4.1 substr. H2 plasmid pB, complete sequence	30334-30366	7	0.788
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP051471	Rhodobacter sphaeroides strain CH10 plasmid pRspCH10B, complete sequence	61365-61397	7	0.788
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP030274	Rhodobacter sphaeroides 2.4.1 plasmid pB, complete sequence	82833-82865	7	0.788
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP015215	Rhodobacter sphaeroides strain MBTLJ-13 plasmid d, complete sequence	46646-46678	7	0.788
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP015291	Rhodobacter sphaeroides strain MBTLJ-20 plasmid c, complete sequence	44704-44736	7	0.788
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP047040	Rhodobacter sphaeroides strain 2.4.1 substr. H2 plasmid pB, complete sequence	30334-30366	7	0.788
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP051471	Rhodobacter sphaeroides strain CH10 plasmid pRspCH10B, complete sequence	61365-61397	7	0.788
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP030274	Rhodobacter sphaeroides 2.4.1 plasmid pB, complete sequence	82833-82865	7	0.788
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP015215	Rhodobacter sphaeroides strain MBTLJ-13 plasmid d, complete sequence	46646-46678	7	0.788
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	1688127-1688159	7	0.788
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	1490683-1490715	7	0.788
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP024582	Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence	359165-359194	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	68139-68168	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_LR134465	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence	102993-103022	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP018464	Xanthomonas euvesicatoria strain LMG930 plasmid pLMG930.1, complete sequence	144404-144433	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NC_041973	Erwinia phage vB_EamM_RAY, complete genome	201694-201723	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	KU886222	Erwinia phage vB_EamM_Special G, complete genome	203747-203776	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	MG655270	Erwinia phage vB_EamM_Mortimer, complete genome	204512-204541	7	0.767
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	KU886223	Erwinia phage vB_EamM_Simmy50, complete genome	201523-201552	7	0.767
NZ_CP023445_16	16.7|7637588|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637588-7637620	33	NZ_AP018829	Asticcacaulis excentricus strain M6 plasmid pASEM-1, complete sequence	141072-141104	7	0.788
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	MN234196	Gordonia phage CloverMinnie, complete genome	41643-41674	7	0.781
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NC_008826	Methylibium petroleiphilum PM1 plasmid RPME01, complete sequence	465184-465215	7	0.781
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	126278-126309	7	0.781
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP012699	Microbacterium sp. No. 7 plasmid B, complete sequence	66299-66330	7	0.781
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	328223-328254	7	0.781
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NC_008270	Rhodococcus jostii RHA1 plasmid pRHL2, complete sequence	155474-155505	7	0.781
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	591872-591904	8	0.758
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	361326-361358	8	0.758
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	591872-591904	8	0.758
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	361326-361358	8	0.758
NZ_CP023445_9	9.2|5327319|35|NZ_CP023445|CRISPRCasFinder	5327319-5327353	35	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	370967-371001	8	0.771
NZ_CP023445_9	9.2|5327319|35|NZ_CP023445|CRISPRCasFinder	5327319-5327353	35	NZ_CP013109	Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence	58423-58457	8	0.771
NZ_CP023445_9	9.2|5327319|35|NZ_CP023445|CRISPRCasFinder	5327319-5327353	35	NZ_CP024309	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3b, complete sequence	445150-445184	8	0.771
NZ_CP023445_9	9.2|5327319|35|NZ_CP023445|CRISPRCasFinder	5327319-5327353	35	NZ_CP013053	Sinorhizobium americanum CCGM7 plasmid B, complete sequence	56738-56772	8	0.771
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NC_006362	Nocardia farcinica IFM 10152 plasmid pNF1, complete sequence	23660-23692	8	0.758
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NC_008697	Nocardioides sp. JS614 plasmid pNOCA01, complete sequence	287896-287928	8	0.758
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	273225-273254	8	0.733
NZ_CP023445_16	16.1|7637222|33|NZ_CP023445|CRISPRCasFinder	7637222-7637254	33	NZ_CP046573	Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence	897164-897196	8	0.758
NZ_CP023445_16	16.1|7637222|33|NZ_CP023445|CRISPRCasFinder	7637222-7637254	33	NZ_CP012699	Microbacterium sp. No. 7 plasmid B, complete sequence	66298-66330	8	0.758
NZ_CP023445_16	16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT	7637283-7637315	33	NZ_CP046574	Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence	385911-385943	8	0.758
NZ_CP023445_16	16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT	7637283-7637315	33	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	1030760-1030792	8	0.758
NZ_CP023445_16	16.7|7637588|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637588-7637620	33	NZ_CP016313	Thermus brockianus strain GE-1 plasmid pTB1, complete sequence	325432-325464	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	MN478374	Bacteriophage Phobos, complete genome	55266-55298	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP021942	Klebsiella pneumoniae strain AR_0145 plasmid tig00000218j2847_linear, complete sequence	32617-32649	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP012429	Klebsiella pneumoniae strain KP5 plasmid pSg1-3, complete sequence	25437-25469	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP017988	Klebsiella pneumoniae strain 825795-1 plasmid unnamed3, complete sequence	32236-32268	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018715	Klebsiella pneumoniae strain Kp_Goe_152021 plasmid pKp_Goe_021-5, complete sequence	43964-43996	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018721	Klebsiella pneumoniae strain KP_Goe_828304 plasmid pKp_Goe_304-5, complete sequence	43589-43621	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018703	Klebsiella pneumoniae strain Kp_Goe_827024 plasmid pKp_Goe_024-5, complete sequence	35288-35320	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_AP023151	Klebsiella pneumoniae strain SMKP03 plasmid pSMKP03S, complete sequence	50184-50216	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP033624	Klebsiella pneumoniae strain 4743 plasmid unnamed6	20820-20852	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP041953	Klebsiella pneumoniae strain KP2 plasmid pKP2_7, complete sequence	31597-31629	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP026270	Klebsiella oxytoca strain KONIH4 plasmid unnamed, complete sequence	20811-20843	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP021957	Klebsiella pneumoniae strain AR_0107 plasmid unitig_3j2_linear_pilon, complete sequence	38864-38896	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP009276	Klebsiella variicola strain DX120E plasmid pKV2, complete sequence	21905-21937	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP028794	Klebsiella pneumoniae strain WCHKP040035 plasmid p1_040035, complete sequence	34254-34286	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP024837	Klebsiella pneumoniae strain CRKP-2297 plasmid pCRKP-2297_3, complete sequence	44972-45004	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP031806	Klebsiella pneumoniae strain MSB1_8A-sc-2280397 plasmid unnamed6, complete sequence	36665-36697	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP027046	Klebsiella pneumoniae strain 1_GR_13 plasmid unnamed, complete sequence	23086-23118	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP024841	Klebsiella pneumoniae strain CRKP-1215 plasmid pCRKP-1215_3, complete sequence	24382-24414	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP036444	Klebsiella pneumoniae strain ABFPV plasmid tig00001255_pilon, complete sequence	52321-52353	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP024433	Klebsiella pneumoniae strain DA48896 plasmid p48896_4, complete sequence	41688-41720	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP050366	Klebsiella pneumoniae strain 47733 plasmid p47733L, complete sequence	23059-23091	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP011631	Klebsiella oxytoca strain CAV1374 plasmid pCAV1374-54, complete sequence	50515-50547	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018314	Klebsiella pneumoniae strain Kp_Goe_822579 plasmid pKp_Goe_579-6, complete sequence	30203-30235	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP032191	Klebsiella pneumoniae strain AR_0075 plasmid unnamed6, complete sequence	45383-45415	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP021949	Klebsiella pneumoniae strain AR_0152 plasmid tig00000216_u, complete sequence	43644-43676	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018688	Klebsiella pneumoniae strain Kp_Goe_149473 plasmid pKp_Goe_473-5, complete sequence	32681-32713	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP034057	Klebsiella pneumoniae strain KP_NORM_BLD_2015_112126 plasmid unnamed4, complete sequence	9410-9442	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP034049	Klebsiella pneumoniae strain KP_NORM_BLD_2014_104014 plasmid unnamed4, complete sequence	4533-4565	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP021760	Klebsiella pneumoniae strain AR_0138 plasmid tig00000003, complete sequence	361-393	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	CP052339	Klebsiella pneumoniae strain D17KP0018 plasmid unnamed	31883-31915	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018697	Klebsiella pneumoniae strain Kp_Goe_149832 plasmid pKp_Goe_832-5, complete sequence	34619-34651	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP018709	Klebsiella pneumoniae strain Kp_Goe_827026 plasmid pKp_Goe_026-5, complete sequence	41696-41728	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP032224	Klebsiella pneumoniae strain AR_0046 plasmid unnamed2, complete sequence	39820-39852	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	MT090961	Klebsiella pneumoniae strain KP18-2079 plasmid pKP18-2079_54kb, complete sequence	22354-22386	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	CP038007	Klebsiella phage 020009, complete genome	32316-32348	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	KY271402	Klebsiella phage 48ST307, complete genome	31172-31204	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	MK416021	Klebsiella phage ST846-OXA48phi9.1, complete genome	17349-17381	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NC_005857	Klebsiella phage phiKO2, complete genome	9967-9999	8	0.758
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	AY374448	Bacteriophage phiKO2, complete genome	9967-9999	8	0.758
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1616675-1616706	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	745365-745396	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	1198925-1198956	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1387019-1387050	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NC_023286	Streptomyces sp. F12 plasmid pFRL6, complete sequence	112326-112357	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	MH697579	Mycobacterium phage Cane17, complete genome	43327-43358	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	MG812494	Mycobacterium phage Pier, complete genome	45935-45966	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	MK359359	Mycobacterium phage Colt, complete genome	43923-43954	8	0.75
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	KX752698	Mycobacterium phage Tonenili, complete genome	49070-49101	8	0.75
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP046573	Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence	897165-897196	8	0.75
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP017750	Cupriavidus sp. USMAA2-4 plasmid unnamed1, complete sequence	364986-365017	8	0.75
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_LN831788	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence	77274-77305	8	0.75
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NC_017858	Methylophaga frappieri strain JAM7 plasmid, complete sequence	21040-21071	8	0.75
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NC_011962	Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence	93720-93752	9	0.727
NZ_CP023445_1	1.3|30298|33|NZ_CP023445|CRT	30298-30330	33	NZ_CP034185	Deinococcus sp. S14-83 strain S14-83T plasmid unnamed1, complete sequence	124270-124302	9	0.727
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NC_011962	Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence	93720-93752	9	0.727
NZ_CP023445_1	1.5|30400|33|NZ_CP023445|CRT	30400-30432	33	NZ_CP034185	Deinococcus sp. S14-83 strain S14-83T plasmid unnamed1, complete sequence	124270-124302	9	0.727
NZ_CP023445_6	6.1|2908183|35|NZ_CP023445|CRISPRCasFinder	2908183-2908217	35	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	426097-426131	9	0.743
NZ_CP023445_6	6.1|2908183|35|NZ_CP023445|CRISPRCasFinder	2908183-2908217	35	MN694593	Marine virus AFVG_250M740, complete genome	24621-24655	9	0.743
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	NZ_CP039640	Azospirillum sp. TSH100 plasmid p1, complete sequence	24069-24103	9	0.743
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	196494-196528	9	0.743
NZ_CP023445_8	8.2|5326941|35|NZ_CP023445|CRISPRCasFinder	5326941-5326975	35	ASHF01000034	Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence	194947-194981	9	0.743
NZ_CP023445_14	14.3|7196403|30|NZ_CP023445|CRT	7196403-7196432	30	NZ_CP032678	Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence	127890-127919	9	0.7
NZ_CP023445_16	16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT	7637283-7637315	33	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	322020-322052	9	0.727
NZ_CP023445_16	16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT	7637344-7637376	33	NZ_CP011665	Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence	397601-397633	9	0.727
NZ_CP023445_16	16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT	7637344-7637376	33	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	236515-236547	9	0.727
NZ_CP023445_16	16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637405-7637437	33	MH271313	Gordonia phage Suzy, complete genome	58641-58673	9	0.727
NZ_CP023445_16	16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637649-7637681	33	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	1542012-1542044	9	0.727
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1434514-1434545	9	0.719
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP027369	Escherichia coli strain 2014C-3307 plasmid unnamed1, complete sequence	9547-9578	9	0.719
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NC_012849	Ralstonia pickettii 12D plasmid pRp12D02, complete sequence	23975-24006	9	0.719
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	MH632120	Mycobacterium phage Thonko, complete genome	45920-45951	9	0.719
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	MN813693	Mycobacterium phage Imvubu, complete genome	44725-44756	9	0.719
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	MT639653	Arthrobacter phage Elezi, complete genome	16274-16308	10	0.714
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	MT889366	Arthrobacter phage London, complete genome	16274-16308	10	0.714
NZ_CP023445_8	8.1|5326878|35|NZ_CP023445|CRISPRCasFinder	5326878-5326912	35	KR053197	Gordonia phage GRU3, complete genome	6455-6489	10	0.714
NZ_CP023445_10	10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT	6009694-6009726	33	NZ_CP053709	Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed1, complete sequence	112026-112058	10	0.697
NZ_CP023445_16	16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637405-7637437	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	768216-768248	10	0.697
NZ_CP023445_16	16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637405-7637437	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1044908-1044940	10	0.697
NZ_CP023445_16	16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR	7637771-7637802	32	NZ_CP032350	Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence	52970-53001	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1114169-1114200	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1143100-1143131	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1519477-1519508	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	551053-551084	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	100595-100626	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	301233-301264	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1592109-1592140	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1597914-1597945	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1770091-1770122	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	418911-418942	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1895955-1895986	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1516744-1516775	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1145849-1145880	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	413602-413633	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	2037440-2037471	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1599560-1599591	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	872453-872484	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	1309208-1309239	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1525844-1525875	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	1557466-1557497	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1522577-1522608	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	780802-780833	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	1517720-1517751	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	1483912-1483943	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1522068-1522099	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1611040-1611071	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	780802-780833	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1575354-1575385	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1609442-1609473	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	780803-780834	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1511683-1511714	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1575666-1575697	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1609442-1609473	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1575354-1575385	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1512329-1512360	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1574557-1574588	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1609442-1609473	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1609442-1609473	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1609442-1609473	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	441723-441754	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1511705-1511736	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1517150-1517181	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1497799-1497830	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1550747-1550778	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1589946-1589977	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1606757-1606788	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1511705-1511736	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1575665-1575696	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1596411-1596442	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	780799-780830	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1511705-1511736	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1511705-1511736	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1609445-1609476	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	435776-435807	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	780805-780836	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	435776-435807	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	JN699011	Mycobacterium phage Stinger, complete genome	45465-45496	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	KY224000	Mycobacterium phage Rich, complete genome	48901-48932	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	KR080199	Mycobacterium phage Baee, complete genome	48605-48636	10	0.688
NZ_CP023445_16	16.12|7637223|32|NZ_CP023445|CRT	7637223-7637254	32	NZ_CP029777	Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence	110252-110283	11	0.656

1. spacer 13.5|6969581|22|NZ_CP023445|CRISPRCasFinder matches to NZ_CP021374 (Rhizobium sp. ACO-34A plasmid pRACO34Ab, complete sequence) position: , mismatch: 1, identity: 0.955

gtcgagcgatcggctgctgggc	CRISPR spacer
gtcgagcgatcggctggtgggc	Protospacer
**************** *****

2. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MG593802 (Streptomyces phage Omar, complete genome) position: , mismatch: 2, identity: 0.926

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggccgtagcc	Protospacer
*. ************************

3. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MH509442 (Mycobacterium phage Aminay, complete genome) position: , mismatch: 2, identity: 0.926

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtcgccgccctggccgttgcc	Protospacer
******** ************** ***

4. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_JX627580 (Methylobacterium oryzae CBMB20 plasmid pMOC1, complete sequence) position: , mismatch: 3, identity: 0.889

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccgtggccgtagcc	Protospacer
*. ************ ***********

5. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MN204498 (Streptomyces phage Saftant, complete genome) position: , mismatch: 3, identity: 0.889

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ccagccgtagccgtcctggccgtagcc	Protospacer
 * **********.*************

6. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to KY676784 (Streptomyces phage ToastyFinz, complete genome) position: , mismatch: 3, identity: 0.9

ccccgcagggttacccgcagcag-ccgccgc	CRISPR spacer
ccccgcagggcgacccgcagcagcccgccg-	Protospacer
**********. *********** ****** 

7. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_AP022607 (Mycobacterium branderi strain JCM 12687 plasmid pJCM12687) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ctggccgtaaccgccctggccgtagcc	Protospacer
 . ******.*****************

8. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_023600 (Mycobacterium phage Jolie1, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggccgagcac	Protospacer
********************** .  *

9. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_022061 (Mycobacterium phage KayaCho, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggccgagcac	Protospacer
********************** .  *

10. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KJ433975 (Mycobacterium phage 40BC, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggccgagcac	Protospacer
********************** .  *

11. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KJ433973 (Mycobacterium phage 39HC, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggccgagcac	Protospacer
********************** .  *

12. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_024145 (Mycobacterium phage Hosp, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggccgagcac	Protospacer
********************** .  *

13. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
cccgccgaacccgccctggccgtagcg	Protospacer
 ****** * **************** 

14. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP018471 (Xanthomonas vesicatoria strain LM159 plasmid pLM159.2, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

15. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_KJ588780 (Achromobacter xylosoxidans strain A22732 plasmid pA22732-IMP, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

16. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_KP289281 (Pseudomonas sp. EGD-AKN5 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

17. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_MN366359 (Bacterium plasmid pALTS31, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

18. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_001735 (Enterobacter aerogenes plasmid R751, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

19. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP015373 (Pandoraea pnomenusa strain MCB032 plasmid unnamed 2, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

20. spacer 1.4|30352|27|NZ_CP023445|CRT matches to AGRM01000006 (Salmonella enterica subsp. houtenae str. ATCC BAA-1581 plasmid pSEHO0A1, complete sequence, whole genome shotgun sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

21. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_017908 (Mycobacterium abscessus subsp. bolletii F1725 plasmid BRA100, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

22. spacer 1.4|30352|27|NZ_CP023445|CRT matches to AJ863570 (Uncultured bacterium IncP-1beta multiresistance plasmid pB8) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

23. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_008459 (Bordetella pertussis plasmid pBP136 DNA, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

24. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KU238092 (Uncultured bacterium plasmid pDTC28, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

25. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JX469834 (Uncultured bacterium plasmid pDS3, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

26. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JX469831 (Uncultured bacterium plasmid pKSP212, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

27. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106172 (Uncultured bacterium plasmid pAKD29, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

28. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106173 (Uncultured bacterium plasmid pAKD31, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

29. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106174 (Uncultured bacterium plasmid pAKD33, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

30. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_004956 (Pseudomonas sp. ADP atrazine catabolic plasmid pADP-1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

31. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106164 (Uncultured bacterium plasmid pAKD1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

32. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106165 (Uncultured bacterium plasmid pAKD14, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

33. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106166 (Uncultured bacterium plasmid pAKD15, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

34. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106168 (Uncultured bacterium plasmid pAKD17, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

35. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JN106169 (Uncultured bacterium plasmid pAKD18, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

36. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_014911 (Alicycliphilus denitrificans BC plasmid pALIDE02, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

37. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MN386974 (Pseudomonas aeruginosa strain 1943 plasmid pPaeBURNS1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

38. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MG879028 (Uncultured bacterium plasmid pEG1-1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

39. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP021650 (Acidovorax sp. T1 plasmid p2-T1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

40. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KF743817 (Proteus mirabilis plasmid R772, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

41. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KF743818 (Bordetella bronchiseptica plasmid R906, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

42. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JX486125 (Uncultured bacterium plasmid pRWC72a, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

43. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP019238 (Rhodoferax koreense strain DCY-110 plasmid unnamed2) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

44. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP038640 (Cupriavidus oxalaticus strain X32 plasmid unnamed5, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

45. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KC170279 (Uncultured bacterium plasmid pMBUI8, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

46. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KU356987 (Variovorax paradoxus plasmid pBS64, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

47. spacer 1.4|30352|27|NZ_CP023445|CRT matches to KU356988 (Variovorax paradoxus plasmid pHB44, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

48. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP009797 (Burkholderia ambifaria AMMD plasmid pBII_1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

49. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_013176 (Pseudomonas putida plasmid pW2, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

50. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_019312 (Delftia sp. KV29 plasmid pKV29, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

51. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_019320 (Variovorax sp. DB1 plasmid pDB1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

52. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP017455 (Dickeya solani strain PPO 9019 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

53. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_021077 (Comamonas sp. 7D-2 plasmid pBHB, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

54. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_007337 (Cupriavidus pinatubonensis JMP134 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

55. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_024998 (Acidovorax avenae subsp. avenae plasmid pAAA83 DNA, complete sequence, strain: 83) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

56. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_MH053445 (Pseudomonas aeruginosa strain PA1280 plasmid pICP-4GES, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

57. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_005088 (Delftia acidovorans B plasmid pUO1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

58. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_008385 (Burkholderia ambifaria AMMD plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgccctggcagaagcc	Protospacer
*. ***************** * ****

59. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MH669016 (Streptomyces phage TrvxScott, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgtcctgggcgtagcc	Protospacer
*. **********.***** *******

60. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MT711979 (Streptomyces phage Endor2, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ccagccgtagccgtcctcgccgtagcc	Protospacer
 * **********.*** *********

61. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MK524524 (Streptomyces phage Caelum, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ccagccgtagccgtcctggtcgtagcc	Protospacer
 * **********.*****.*******

62. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MK392365 (Streptomyces phage TinaBelcher, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgtcctgggcgtagcc	Protospacer
*. **********.***** *******

63. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MH651190 (Streptomyces phage Thestral, complete genome) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gtagccgtagccgtcctgggcgtagcc	Protospacer
*. **********.***** *******

64. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

65. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_LR134456 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence) position: , mismatch: 4, identity: 0.852

gccgcc-gtagccgccctggccgtagcc	CRISPR spacer
-ctgctggtagccgccctggtcgtagcc	Protospacer
 *.**. *************.*******

66. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

67. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP025614 (Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed2, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtggccgccctggccaacgcc	Protospacer
********.************.  ***

68. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

69. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

70. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

71. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 4, identity: 0.852

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
gatgccgtagccgccctggccg--gccag	Protospacer
* .*******************  ***  

72. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NZ_CP035092 (Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
catggcggcgatcacccagcccgtg	Protospacer
*.************ ********. 

73. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NC_008688 (Paracoccus denitrificans PD1222 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
catggcggcgatcacccagcccgtg	Protospacer
*.************ ********. 

74. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NC_017966 (Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
ggtggcggcgatcaaccagcaggcg	Protospacer
 *******************  ** 

75. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NZ_CP010683 (Phaeobacter piscinae strain P14 plasmid pP14_b, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
gctggcggcgatgacccagcccgcc	Protospacer
  ********** * **********

76. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NZ_CP010718 (Phaeobacter piscinae strain P18 plasmid pP18_c, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
gctggcggcgatgacccagcccgcc	Protospacer
  ********** * **********

77. spacer 3.1|1316611|25|NZ_CP023445|CRISPRCasFinder matches to NZ_CP010859 (Marinovum algicola DG 898 plasmid pMaD4, complete sequence) position: , mismatch: 4, identity: 0.84

cgtggcggcgatcaaccagcccgcc	CRISPR spacer
tgcggcggcgatcgaccagcccgct	Protospacer
.*.**********.**********.

78. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP049751 (Rhodococcus fascians A21d2 plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtagccgccctggctgcgggt	Protospacer
********************.*..* .

79. spacer 1.4|30352|27|NZ_CP023445|CRT matches to LR134127 (Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
accgccgtcgccgccctggccgttagc	Protospacer
.******* ************** . *

80. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP009803 (Streptomyces sp. FR-008 plasmid pSSFR1, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtcgccgccctggccgacgag	Protospacer
******** *************  *  

81. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP009803 (Streptomyces sp. FR-008 plasmid pSSFR1, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgttgccgccctggccgacgag	Protospacer
******** *************  *  

82. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
cccgccgtcgccgccctggacgtagtg	Protospacer
 ******* ********** *****. 

83. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
cccgccgtcgccgccctggacgtagtg	Protospacer
 ******* ********** *****. 

84. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP022220 (Bradyrhizobium guangxiense strain CCBAU 53363 plasmid p53363, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ctcgccgtagccgccctggcaatagac	Protospacer
 .****************** .*** *

85. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc--	CRISPR spacer
aatgccgtagccgccctggccg--gccag	Protospacer
. .*******************  ***  

86. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_AP021877 (Desulfosarcina ovata strain 28bB2T plasmid Do28_1, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gaggccgtagccgccctggccggtgcg	Protospacer
*  *******************  ** 

87. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP030052 (Bradyrhizobium guangdongense strain CCBAU 51649 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ctcgccgtagccgccctggcaatagac	Protospacer
 .****************** .*** *

88. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP030054 (Bradyrhizobium guangzhouense strain CCBAU 51670 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ctcgccgtagccgccctggcaatagac	Protospacer
 .****************** .*** *

89. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP041045 (Paracoccus sp. AK26 plasmid pAK1, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ggcgccgttgccgccctggccgtccgc	Protospacer
* ****** **************   *

90. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_015721 (Bdellovibrio phage phi1402, complete genome) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccggagccgccctggcctttttc	Protospacer
******* ************* *  .*

91. spacer 1.4|30352|27|NZ_CP023445|CRT matches to JF344709 (Bdellovibrio phage phi1402, complete sequence) position: , mismatch: 5, identity: 0.815

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccggagccgccctggcctttttc	Protospacer
******* ************* *  .*

92. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP033195 (Xanthomonas oryzae pv. oryzae strain CIAT plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ccccgcagggctacccgcagcagtacccgg	Protospacer
**********.************.  *** 

93. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP022994 (Paraburkholderia aromaticivorans strain BN5 plasmid pBN4, complete sequence) position: , mismatch: 5, identity: 0.833

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ccccgcagggctacccgcagcagtatccgg	Protospacer
**********.************.  *** 

94. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP026110 (Paraburkholderia hospita strain DSM 17164 plasmid pEMT1, complete sequence) position: , mismatch: 5, identity: 0.833

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ccccgcagggctacccgcagcagtatccgg	Protospacer
**********.************.  *** 

95. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to CP000620 (Burkholderia vietnamiensis G4 plasmid pBVIE04, complete sequence) position: , mismatch: 5, identity: 0.833

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ccccgcagggctacccgcagcagtatccgg	Protospacer
**********.************.  *** 

96. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP033202 (Xanthomonas oryzae pv. oryzae strain BXO1 plasmid pBXO1-1, complete sequence) position: , mismatch: 5, identity: 0.833

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ccccgcagggctacccgcagcagtacccgg	Protospacer
**********.************.  *** 

97. spacer 16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_LR134450 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 8, complete sequence) position: , mismatch: 5, identity: 0.848

ggccgggtcgacgcggacgcggacg-tactcgcc	CRISPR spacer
ggcctcgtcgacgcggacgcggacgctgttcgc-	Protospacer
****  ******************* *..**** 

98. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

99. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

100. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
accggcaccctgcttgccgccctggccgtggcc	Protospacer
.***  .******* **************.***

101. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

102. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

103. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctg--gccgtagcc	CRISPR spacer
gcagtggccctgctggccgccctgatgccatgg--	Protospacer
** **.******************  ***.*.*  

104. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gatgccgtagccgccctggccggcgag	Protospacer
* .*******************  *  

105. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gatgccgtagccgccctggccggcgag	Protospacer
* .*******************  *  

106. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP045122 (Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ctcgccgtcgccgccctggccgtgctc	Protospacer
 .****** **************. .*

107. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
accgccgtagccgccctggtcggggta	Protospacer
.******************.** .*. 

108. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NZ_CP025547 (Mycobacterium paragordonae strain 49061 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgttgccgccctggccaccgga	Protospacer
******** ************.. *  

109. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_007950 (Polaromonas sp. JS666 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
ggtaccgtacccgccctggccgtagaa	Protospacer
* ..***** ***************  

110. spacer 1.4|30352|27|NZ_CP023445|CRT matches to MN908689 (Arthrobacter phage DrSierra, complete genome) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgacgtggccgccctggccgtcaag	Protospacer
**** ***.************** .  

111. spacer 1.4|30352|27|NZ_CP023445|CRT matches to LR743530 (Xanthomonas phage Suba genome assembly, chromosome: 1) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgttgccgccctggccctgctg	Protospacer
******** ************ *. . 

112. spacer 1.4|30352|27|NZ_CP023445|CRT matches to NC_049432 (Ralstonia phage RsoM1USA, complete genome) position: , mismatch: 6, identity: 0.778

gccgccgtagccgccctggccgtagcc	CRISPR spacer
gccgccgtcgccgccctgggcgtgtgg	Protospacer
******** ********** ***.   

113. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

114. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

115. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NC_016585 (Azospirillum lipoferum 4B plasmid AZO_p1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
accggcaccctgcttgccgccctggccgtggcc	Protospacer
.***  .******* **************.***

116. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

117. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gacgaagccctgctggccgccctggtcgccgac	Protospacer
* ** ********************.**. * *

118. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP026305 (Streptomyces lunaelactis strain MM109 plasmid pSLUN1, complete sequence) position: , mismatch: 6, identity: 0.818

gccgtagccctgctggccgccctg--gccgtagcc	CRISPR spacer
gcagtggccctgctggccgccctgatgccatgg--	Protospacer
** **.******************  ***.*.*  

119. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to NZ_CP011274 (Planctomyces sp. SH-PL62 plasmid pPL62-1, complete sequence) position: , mismatch: 6, identity: 0.829

tcggcgacgacgcggccgaaggcgtcgcgctcgaa---	CRISPR spacer
tcggcgacgacgcggccgagggcttcg---gcgaaccc	Protospacer
*******************.*** ***    ****   

120. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP022607 (Mycobacterium branderi strain JCM 12687 plasmid pJCM12687) position: , mismatch: 6, identity: 0.818

cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
ctcatcggcggcctcgatcaggtccacgacccg	Protospacer
* .  *.************************.*

121. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 6, identity: 0.8

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
cccagcaggggtacccgcagcagcaggggt	Protospacer
*** ****** ************* *  *.

122. spacer 16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 6, identity: 0.818

ggccgggtcgacgcggacgcggacgt-actcgcc	CRISPR spacer
gtccgggtcgacccggacgcggccgtgacccgg-	Protospacer
* ********** ********* *** **.**  

123. spacer 16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_CP051543 (Paracoccus sanguinis strain OM2164 plasmid pPspOM122, complete sequence) position: , mismatch: 6, identity: 0.818

ttcatgcgcgccctgaagcgggtcgcggtctac	CRISPR spacer
ttcctgcgcgccctgaagcaggtcgccgccgag	Protospacer
*** ***************.****** *.* * 

124. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.812

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgccgttccacgcggaccagctcgacgtgcac	Protospacer
*  *  ******************.* *****

125. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP015291 (Rhodobacter sphaeroides strain MBTLJ-20 plasmid c, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

126. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP047040 (Rhodobacter sphaeroides strain 2.4.1 substr. H2 plasmid pB, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

127. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP051471 (Rhodobacter sphaeroides strain CH10 plasmid pRspCH10B, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

128. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP030274 (Rhodobacter sphaeroides 2.4.1 plasmid pB, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

129. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP015215 (Rhodobacter sphaeroides strain MBTLJ-13 plasmid d, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

130. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP015291 (Rhodobacter sphaeroides strain MBTLJ-20 plasmid c, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

131. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP047040 (Rhodobacter sphaeroides strain 2.4.1 substr. H2 plasmid pB, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

132. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP051471 (Rhodobacter sphaeroides strain CH10 plasmid pRspCH10B, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

133. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP030274 (Rhodobacter sphaeroides 2.4.1 plasmid pB, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

134. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP015215 (Rhodobacter sphaeroides strain MBTLJ-13 plasmid d, complete sequence) position: , mismatch: 7, identity: 0.788

gccgtagccctgctggccgccctggccgtagcc---	CRISPR spacer
gccctggccctgctggccgccctgcc---ggcctgg	Protospacer
*** *.****************** *   .***   

135. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 7, identity: 0.788

cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
ggcggcatcggcctcgatcagatccacgaccac	Protospacer
 *. *** *************.*********  

136. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 7, identity: 0.788

cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
ggcggcatcggcctcgatcagatccacgaccac	Protospacer
 *. *** *************.*********  

137. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP024582 (Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
gtggccagggtttcccgcagcagccgctgc	Protospacer
 .   ******* **************.**

138. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
gtggccagggtttcccgcagcagccgctgc	Protospacer
 .   ******* **************.**

139. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_LR134465 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
agcaggggggatacccgcagcagcccccgc	Protospacer
  * * .*** ************** ****

140. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP018464 (Xanthomonas euvesicatoria strain LMG930 plasmid pLMG930.1, complete sequence) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
ctccgcagggctacccgcagcagtattcgg	Protospacer
*.********.************.  .** 

141. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NC_041973 (Erwinia phage vB_EamM_RAY, complete genome) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
tgcagcagggttacccgcaacagccacaga	Protospacer
. * ***************.*****.* * 

142. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to KU886222 (Erwinia phage vB_EamM_Special G, complete genome) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
tgcagcagggttacccgcaacagccacaga	Protospacer
. * ***************.*****.* * 

143. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to MG655270 (Erwinia phage vB_EamM_Mortimer, complete genome) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
tgcagcagggttacccgcaacagccacaga	Protospacer
. * ***************.*****.* * 

144. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to KU886223 (Erwinia phage vB_EamM_Simmy50, complete genome) position: , mismatch: 7, identity: 0.767

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
tgcagcagggttacccgcaacagccacaga	Protospacer
. * ***************.*****.* * 

145. spacer 16.7|7637588|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP018829 (Asticcacaulis excentricus strain M6 plasmid pASEM-1, complete sequence) position: , mismatch: 7, identity: 0.788

gcggtcatcgcctcgtcgaggtcc--aacccgccc	CRISPR spacer
gcggtcatcgcctcggcgcggtccgtagtcagc--	Protospacer
*************** ** *****  *..* **  

146. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MN234196 (Gordonia phage CloverMinnie, complete genome) position: , mismatch: 7, identity: 0.781

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgaccatccccgccgaccagctcggcgtcgtc	Protospacer
* ******* *** ************ *   *

147. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_008826 (Methylibium petroleiphilum PM1 plasmid RPME01, complete sequence) position: , mismatch: 7, identity: 0.781

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
ccgccgaagacgcgcaccagcgcggcctgcac	Protospacer
**.**.   ***** ****** **********

148. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 7, identity: 0.781

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
ccatggcccacgcggaccagcttgtcctgcgc	Protospacer
***. ..***************.* *****.*

149. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP012699 (Microbacterium sp. No. 7 plasmid B, complete sequence) position: , mismatch: 7, identity: 0.781

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
acgtcgacatctacggcaacgaccgcgtctac	Protospacer
*.. **  ****** ************ ****

150. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 7, identity: 0.781

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
acaccgcgatcgaccgcagcgaccgcgccgtc	Protospacer
*.* ******* ******.******** *  *

151. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NC_008270 (Rhodococcus jostii RHA1 plasmid pRHL2, complete sequence) position: , mismatch: 7, identity: 0.781

atagcgc----gatctaccgcaacgaccgcggctac	CRISPR spacer
----cgctgctgatctaccgcaacgacggcgcctcc	Protospacer
    ***    **************** *** ** *

152. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.758

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccgtcaccctgctggccgccctgtggctggcg	Protospacer
***** .*****************    *.** 

153. spacer 1.3|30298|33|NZ_CP023445|CRT matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.758

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccgtcgccctgctggccgtcctgcgggccggc	Protospacer
***** *************.****   *. * *

154. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.758

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccgtcaccctgctggccgccctgtggctggcg	Protospacer
***** .*****************    *.** 

155. spacer 1.5|30400|33|NZ_CP023445|CRT matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.758

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccgtcgccctgctggccgtcctgcgggccggc	Protospacer
***** *************.****   *. * *

156. spacer 9.2|5327319|35|NZ_CP023445|CRISPRCasFinder matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.771

tcgcggatgacccgaccgcgctcgtcgaggtcgta	CRISPR spacer
ccgcggatgacctgaccgcgctcgacgtcatgata	Protospacer
.***********.*********** **  .* .**

157. spacer 9.2|5327319|35|NZ_CP023445|CRISPRCasFinder matches to NZ_CP013109 (Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence) position: , mismatch: 8, identity: 0.771

tcgcggatgacccgaccgcgctcgtcgaggtcgta	CRISPR spacer
tcgagatcgacccgaccgcgctcgttgaggacgac	Protospacer
*** *. .*****************.**** **  

158. spacer 9.2|5327319|35|NZ_CP023445|CRISPRCasFinder matches to NZ_CP024309 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3b, complete sequence) position: , mismatch: 8, identity: 0.771

tcgcggatgacccgaccgcgctcgtcgaggtcgta	CRISPR spacer
tcgagatcgacccgaccgcgctcgttgaggacgac	Protospacer
*** *. .*****************.**** **  

159. spacer 9.2|5327319|35|NZ_CP023445|CRISPRCasFinder matches to NZ_CP013053 (Sinorhizobium americanum CCGM7 plasmid B, complete sequence) position: , mismatch: 8, identity: 0.771

tcgcggatgacccgaccgcgctcgtcgaggtcgta	CRISPR spacer
tcgagatcgacccgaccgcgctcgttgaggacgac	Protospacer
*** *. .*****************.**** **  

160. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NC_006362 (Nocardia farcinica IFM 10152 plasmid pNF1, complete sequence) position: , mismatch: 8, identity: 0.758

cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
cacggcagcggccgcgatcaggtcaacgatcat	Protospacer
*.. ********* ********** ****.*  

161. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NC_008697 (Nocardioides sp. JS614 plasmid pNOCA01, complete sequence) position: , mismatch: 8, identity: 0.758

-cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
gtgccg-gccggcctcgagcaggtccgcgacctc	Protospacer
 .*.** . ********* *******.****** 

162. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.733

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
cggtgttcggttaccggcagcagccgccgg	Protospacer
*  .*.  ******* ************* 

163. spacer 16.1|7637222|33|NZ_CP023445|CRISPRCasFinder matches to NZ_CP046573 (Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence) position: , mismatch: 8, identity: 0.758

gatagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
gtctgcgcgatctaccccgacgaccgcgacacc	Protospacer
* . ************ *.*********.*  *

164. spacer 16.1|7637222|33|NZ_CP023445|CRISPRCasFinder matches to NZ_CP012699 (Microbacterium sp. No. 7 plasmid B, complete sequence) position: , mismatch: 8, identity: 0.758

gatagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
aacgtcgacatctacggcaacgaccgcgtctac	Protospacer
.*.. **  ****** ************ ****

165. spacer 16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_CP046574 (Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence) position: , mismatch: 8, identity: 0.758

ggccgggtcgacgcggacgcggacgtactcgcc	CRISPR spacer
ggccgggtcggcgcggacccggacgccgtgggt	Protospacer
**********.******* ******.  * * .

166. spacer 16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 8, identity: 0.758

ggccgggtcgacgcggacgcgga-cgtactcgcc	CRISPR spacer
ggccgggtcgaggcggatgcggaccgggaccgt-	Protospacer
*********** *****.***** ** . .**. 

167. spacer 16.7|7637588|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016313 (Thermus brockianus strain GE-1 plasmid pTB1, complete sequence) position: , mismatch: 8, identity: 0.758

gcggtcatcgcctcgtcgaggtccaacccgccc	CRISPR spacer
gcggtcaccgcctcgtagaggtccatttcttcg	Protospacer
*******.******** ******** ..* .* 

168. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MN478374 (Bacteriophage Phobos, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
tatgtgaagaagccgaacgcggcgggcgtgaat	Protospacer
 ..******** *.*************** .* 

169. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021942 (Klebsiella pneumoniae strain AR_0145 plasmid tig00000218j2847_linear, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

170. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012429 (Klebsiella pneumoniae strain KP5 plasmid pSg1-3, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

171. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017988 (Klebsiella pneumoniae strain 825795-1 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

172. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018715 (Klebsiella pneumoniae strain Kp_Goe_152021 plasmid pKp_Goe_021-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

173. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018721 (Klebsiella pneumoniae strain KP_Goe_828304 plasmid pKp_Goe_304-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

174. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018703 (Klebsiella pneumoniae strain Kp_Goe_827024 plasmid pKp_Goe_024-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

175. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP023151 (Klebsiella pneumoniae strain SMKP03 plasmid pSMKP03S, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

176. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033624 (Klebsiella pneumoniae strain 4743 plasmid unnamed6) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

177. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP041953 (Klebsiella pneumoniae strain KP2 plasmid pKP2_7, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

178. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026270 (Klebsiella oxytoca strain KONIH4 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

179. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021957 (Klebsiella pneumoniae strain AR_0107 plasmid unitig_3j2_linear_pilon, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

180. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009276 (Klebsiella variicola strain DX120E plasmid pKV2, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

181. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP028794 (Klebsiella pneumoniae strain WCHKP040035 plasmid p1_040035, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

182. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024837 (Klebsiella pneumoniae strain CRKP-2297 plasmid pCRKP-2297_3, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

183. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031806 (Klebsiella pneumoniae strain MSB1_8A-sc-2280397 plasmid unnamed6, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

184. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027046 (Klebsiella pneumoniae strain 1_GR_13 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

185. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024841 (Klebsiella pneumoniae strain CRKP-1215 plasmid pCRKP-1215_3, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

186. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP036444 (Klebsiella pneumoniae strain ABFPV plasmid tig00001255_pilon, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

187. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024433 (Klebsiella pneumoniae strain DA48896 plasmid p48896_4, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

188. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050366 (Klebsiella pneumoniae strain 47733 plasmid p47733L, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

189. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP011631 (Klebsiella oxytoca strain CAV1374 plasmid pCAV1374-54, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

190. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018314 (Klebsiella pneumoniae strain Kp_Goe_822579 plasmid pKp_Goe_579-6, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

191. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032191 (Klebsiella pneumoniae strain AR_0075 plasmid unnamed6, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

192. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021949 (Klebsiella pneumoniae strain AR_0152 plasmid tig00000216_u, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

193. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018688 (Klebsiella pneumoniae strain Kp_Goe_149473 plasmid pKp_Goe_473-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

194. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP034057 (Klebsiella pneumoniae strain KP_NORM_BLD_2015_112126 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

195. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP034049 (Klebsiella pneumoniae strain KP_NORM_BLD_2014_104014 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

196. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021760 (Klebsiella pneumoniae strain AR_0138 plasmid tig00000003, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

197. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to CP052339 (Klebsiella pneumoniae strain D17KP0018 plasmid unnamed) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

198. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018697 (Klebsiella pneumoniae strain Kp_Goe_149832 plasmid pKp_Goe_832-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

199. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018709 (Klebsiella pneumoniae strain Kp_Goe_827026 plasmid pKp_Goe_026-5, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

200. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032224 (Klebsiella pneumoniae strain AR_0046 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

201. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MT090961 (Klebsiella pneumoniae strain KP18-2079 plasmid pKP18-2079_54kb, complete sequence) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

202. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to CP038007 (Klebsiella phage 020009, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

203. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to KY271402 (Klebsiella phage 48ST307, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

204. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MK416021 (Klebsiella phage ST846-OXA48phi9.1, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

205. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_005857 (Klebsiella phage phiKO2, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

206. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to AY374448 (Bacteriophage phiKO2, complete genome) position: , mismatch: 8, identity: 0.758

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
ggcgtggagaacctgaatgcggcgtctatcctg	Protospacer
******.**********.******  ..**  *

207. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgctggtccacgccgaccagctcggcctgccg	Protospacer
*  . .******* ****************  

208. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgctggtccacgccgaccagctcggcctgccg	Protospacer
*  . .******* ****************  

209. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgctggtccacgccgaccagctcggcctgccg	Protospacer
*  . .******* ****************  

210. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgctggtccacgccgaccagctcggcctgccg	Protospacer
*  . .******* ****************  

211. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_023286 (Streptomyces sp. F12 plasmid pFRL6, complete sequence) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
ccgaactggacgcggacctgctcggccagcac	Protospacer
**.   *  ********* ******** ****

212. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MH697579 (Mycobacterium phage Cane17, complete genome) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cggtcgccctcgcggatcagctcggcctgctc	Protospacer
* ..*..** ******.************* *

213. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MG812494 (Mycobacterium phage Pier, complete genome) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cggtcgccctcgcggatcagctcggcctgctc	Protospacer
* ..*..** ******.************* *

214. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MK359359 (Mycobacterium phage Colt, complete genome) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cggtcgccctcgcggatcagctcggcctgctc	Protospacer
* ..*..** ******.************* *

215. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to KX752698 (Mycobacterium phage Tonenili, complete genome) position: , mismatch: 8, identity: 0.75

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cggtcgccctcgcggatcagctcggcctgctc	Protospacer
* ..*..** ******.************* *

216. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP046573 (Rhodococcus sp. WAY2 plasmid pRWAY01, complete sequence) position: , mismatch: 8, identity: 0.75

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
tctgcgcgatctaccccgacgaccgcgacacc	Protospacer
 . ************ *.*********.*  *

217. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP017750 (Cupriavidus sp. USMAA2-4 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
acgacaagttcaacctcaacgaccgcggctac	Protospacer
*...*. * ** *** ****************

218. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_LN831788 (Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence) position: , mismatch: 8, identity: 0.75

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
acaagccgatctacgccaacgaccgcggcatc	Protospacer
*.*.  ********  *************  *

219. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NC_017858 (Methylophaga frappieri strain JAM7 plasmid, complete sequence) position: , mismatch: 8, identity: 0.75

atagcgcgatctaccgcaacgac----cgcggctac	CRISPR spacer
ataacgcgatctaccgcaccgacttgatgcag----	Protospacer
***.************** ****    .**.*    

220. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NC_011962 (Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence) position: , mismatch: 9, identity: 0.727

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccctggccctgctggccgccctgccggcttgg	Protospacer
*** *.****************** * *.    

221. spacer 1.3|30298|33|NZ_CP023445|CRT matches to NZ_CP034185 (Deinococcus sp. S14-83 strain S14-83T plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
ttgatggggctgctggccgccctcgccggagcc	Protospacer
 . .*.*  ************** **** ****

222. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NC_011962 (Rhodobacter sphaeroides KD131 plasmid pRSKD131A, complete sequence) position: , mismatch: 9, identity: 0.727

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
gccctggccctgctggccgccctgccggcttgg	Protospacer
*** *.****************** * *.    

223. spacer 1.5|30400|33|NZ_CP023445|CRT matches to NZ_CP034185 (Deinococcus sp. S14-83 strain S14-83T plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

gccgtagccctgctggccgccctggccgtagcc	CRISPR spacer
ttgatggggctgctggccgccctcgccggagcc	Protospacer
 . .*.*  ************** **** ****

224. spacer 6.1|2908183|35|NZ_CP023445|CRISPRCasFinder matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 9, identity: 0.743

cgcttccacccgctccgcccccgcctccccctgct	CRISPR spacer
ggccaccacccgctccgcccccgcctgcccggcgg	Protospacer
 **. ********************* ***     

225. spacer 6.1|2908183|35|NZ_CP023445|CRISPRCasFinder matches to MN694593 (Marine virus AFVG_250M740, complete genome) position: , mismatch: 9, identity: 0.743

cgcttccacccgctccgcccccgcctccccctgct	CRISPR spacer
ttcggctacccgctccgcctccgcctccacctccg	Protospacer
. *  *.************.******** *** * 

226. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to NZ_CP039640 (Azospirillum sp. TSH100 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.743

tcggcgacgacgcggccgaaggcgtcgcgctcgaa	CRISPR spacer
atggcgacggcgcggcggaaggcgtcggcgtcgcg	Protospacer
 .*******.****** **********   *** .

227. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 9, identity: 0.743

tcggcgacgacgcggccgaaggcgtcgcgctcgaa	CRISPR spacer
atggcgacggcgcggcggaaggcgtcggcgtcgcg	Protospacer
 .*******.****** **********   *** .

228. spacer 8.2|5326941|35|NZ_CP023445|CRISPRCasFinder matches to ASHF01000034 (Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence) position: , mismatch: 9, identity: 0.743

agctcggtgatcaggcccgcggcgtcggtgcggta	CRISPR spacer
gcctcggtgatcaggccagcgacgtcggcgacctc	Protospacer
. *************** ***.******.*   * 

229. spacer 14.3|7196403|30|NZ_CP023445|CRT matches to NZ_CP032678 (Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence) position: , mismatch: 9, identity: 0.7

ccccgcagggttacccgcagcagccgccgc	CRISPR spacer
aaggtcagggtgacctgcagcagccgccag	Protospacer
     ****** ***.************. 

230. spacer 16.2|7637283|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.727

ggccgggtcgacgcggacgcggacgtactcgcc	CRISPR spacer
gatcacctcgacgcggtcgcggacgtcctcggg	Protospacer
*..*.  ********* ********* ****  

231. spacer 16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_CP011665 (Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence) position: , mismatch: 9, identity: 0.727

ttcatgcgcgccctgaagcgggtcgcggtctac	CRISPR spacer
cccgtgcacgccctgaaccgggtcgcgggggag	Protospacer
..*.***.********* **********   * 

232. spacer 16.3|7637344|33|NZ_CP023445|CRISPRCasFinder,CRT matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 9, identity: 0.727

ttcatgcgcgccctgaagcgggtcgcggtctac	CRISPR spacer
cccgtgcacgccctgaaccgggtcgcgggggag	Protospacer
..*.***.********* **********   * 

233. spacer 16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to MH271313 (Gordonia phage Suzy, complete genome) position: , mismatch: 9, identity: 0.727

gatctggcggtcccggccagcgggttcgccctg	CRISPR spacer
ccgcaggcgttcccggcaagcgggttcgcgttt	Protospacer
   * **** ******* *********** .* 

234. spacer 16.8|7637649|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 9, identity: 0.727

ggcgtgaagaacctgaacgcggcgggcgtcgag	CRISPR spacer
cttgctgaaaacctgaaagcggcgggcatcgag	Protospacer
  .*. .*.******** *********.*****

235. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 9, identity: 0.719

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
cgctggtccacgccgaccggctcggcctgccg	Protospacer
*  . .******* ****.***********  

236. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027369 (Escherichia coli strain 2014C-3307 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
ctgcgctccccgcggaccagctgggcctgttg	Protospacer
*..*  *** ************ ******.  

237. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_012849 (Ralstonia pickettii 12D plasmid pRp12D02, complete sequence) position: , mismatch: 9, identity: 0.719

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
gtgcccgccacacggaacagctcggcctgcgg	Protospacer
 ..**  ****.**** *************. 

238. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to MH632120 (Mycobacterium phage Thonko, complete genome) position: , mismatch: 9, identity: 0.719

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgccacgatgtaccgcaacgagcgcggcgtc	Protospacer
 .. *.**** *********** ******  *

239. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to MN813693 (Mycobacterium phage Imvubu, complete genome) position: , mismatch: 9, identity: 0.719

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgccacgatgtaccgcaacgagcgcggcgtc	Protospacer
 .. *.**** *********** ******  *

240. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to MT639653 (Arthrobacter phage Elezi, complete genome) position: , mismatch: 10, identity: 0.714

tcggcgacgacgcggccgaaggcgtcgcgctcgaa	CRISPR spacer
gcggcgtcggcgcggccgaaggcgtcgataatgtc	Protospacer
 ***** **.*****************    .*  

241. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to MT889366 (Arthrobacter phage London, complete genome) position: , mismatch: 10, identity: 0.714

tcggcgacgacgcggccgaaggcgtcgcgctcgaa	CRISPR spacer
gcggcgtcggcgcggccgaaggcgtcgataatgtc	Protospacer
 ***** **.*****************    .*  

242. spacer 8.1|5326878|35|NZ_CP023445|CRISPRCasFinder matches to KR053197 (Gordonia phage GRU3, complete genome) position: , mismatch: 10, identity: 0.714

tcggcgacgacgcggccgaaggcgtc-----gcgctcgaa	CRISPR spacer
gcgtcgacgacgcggccgagggcgtcagtgagtgt-----	Protospacer
 ** ***************.******     *.*.     

243. spacer 10.2|6009694|33|NZ_CP023445|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053709 (Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

cgtcgcagcggcctcgatcaggtccacgacctg	CRISPR spacer
tgcgatagcggccgccatcaggtccacgacacc	Protospacer
.*. ..******* * ************** . 

244. spacer 16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 10, identity: 0.697

gatctggcggtcccggccagcgggttcgccctg	CRISPR spacer
cgcacgatcgtcccgggcagcaggttcgccctg	Protospacer
 .. .*.. ******* ****.***********

245. spacer 16.4|7637405|33|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 10, identity: 0.697

gatctggcggtcccggccagcgggttcgccctg	CRISPR spacer
cgcacgatcgtcccgggcagcaggttcgccctg	Protospacer
 .. .*.. ******* ****.***********

246. spacer 16.10|7637771|32|NZ_CP023445|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032350 (Azospirillum brasilense strain MTCC4039 plasmid p5, complete sequence) position: , mismatch: 10, identity: 0.688

ccaccatccacgcggaccagctcggcctgcac	CRISPR spacer
tgggcgcggacgcggaccagatcggcctccac	Protospacer
. . *..  *********** ******* ***

247. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

248. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

249. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

250. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

251. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

252. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

253. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

254. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

255. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

256. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

257. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

258. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

259. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

260. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

261. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

262. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

263. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

264. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

265. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

266. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

267. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

268. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

269. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

270. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

271. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

272. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

273. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

274. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

275. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

276. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

277. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

278. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

279. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

280. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

281. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

282. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

283. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

284. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

285. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

286. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

287. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

288. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

289. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

290. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

291. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

292. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

293. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

294. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

295. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

296. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

297. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

298. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

299. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

300. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

301. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

302. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

303. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

304. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

305. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

306. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

307. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

308. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgaagagatctaccgcaactaccgcgactgg	Protospacer
 ... * ************* ******.**. 

309. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to JN699011 (Mycobacterium phage Stinger, complete genome) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgccacgatgtaccgcaacgagcgcggcgtg	Protospacer
 .. *.**** *********** ******   

310. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to KY224000 (Mycobacterium phage Rich, complete genome) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgcgacgatgtaccgcaacgagcgcggcgtc	Protospacer
 ..  .**** *********** ******  *

311. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to KR080199 (Mycobacterium phage Baee, complete genome) position: , mismatch: 10, identity: 0.688

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
ccgcgacgatgtaccgcaacgagcgcggcgtc	Protospacer
 ..  .**** *********** ******  *

312. spacer 16.12|7637223|32|NZ_CP023445|CRT matches to NZ_CP029777 (Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence) position: , mismatch: 11, identity: 0.656

atagcgcgatctaccgcaacgaccgcggctac	CRISPR spacer
tggccgcgatctaccgcagcgcccgcgagcgt	Protospacer
  . **************.** *****. ...

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	5933194 : 5947561	16	Gordonia_phage(77.78%)	portal,tail	NA
DBSCAN-SWA_2	6738135 : 6789691	43	Neodiprion_abietis_NPV(25.0%)	tRNA,protease	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP023445|5933194:5947561|DBSCAN-SWA
CCTACCGCCTGGTGCGGGCCTGCCACGCGGCGGTGCTGGAGATCACCGCGGCCATGACGTGTGCGTCCTGGTTGCGCTGCACCGAGATGTTGTTGGTGATCACCGGTACGCCGGTGGCGGCAGCGCTGGCGGGTACCGGCGCCGACGCTGCCGGGGTGGCCAGCCCGCCCGAGGCGAACCGGCGGATCAGGTCGTAGCCCATCAACCGCGCGGTCTCGGCGAGGATGCCGGTCGAACGCGTCGACCCGTTCACCGGGATGTACGCCTCCCGGTGGGTCATCCGGTCCCCGATCACCCGCCAGGTGTTCGGATCGACGAACTGAGCCCACCCGCCGCGCATCGGCGTGAGCGGGTGGATGCCGCCGTCGGCGTAGGCCACGACGGACGGGGCGAGCAGGTTGCCGTCGTGGTTGACCGCCATCGGACCGTTGGGCATGGATTTGCCGCTGGTGTAGATGACCGTGACGTACTTCGTGGCCGGTGCGGTGGCGGCGGCGATCTTCTGATTGAAGTCGGAATCGTTGCCCCGCAACACGATCTCCTTGCCGCCGGGCACGTTGTTGACTTCCAGCCCGACCGCGCGCAACCGCTCGACGGCCTGGTCCGACAGCGTCTCCACCGTGATGCTGCGGCGGTCCGGTACCTGCTCGGCCTGCCACTTGAGCAACTGGAGTTCCAGCGTGGTCTTGTCGACGTCCTGGGCATCGATCAGCGTGACCACCTGGCTGGGGAGCAACCCGTACTGGTTCGCCAGCGCCTCGGCCTCGGCGCGGCCGATGCCCATAGCCTCGGCCGCCGCGTAGAACCCGTCACGTGCGCTGGCGACCTCGGCACCCGCTTTCGCCAGCGCCGTCGTGACGTCCTCGCCCTGCGCCCGCGCCAGCTCGTAGGTTTTCAGCGCGGTGTCAGCGGTGGCATCGCGCAGGTCGGTCAACACGCTGTGCAGCCCGCGGGCGTTCTCCTGCGTCGTGTCCAAGCGTCCCTGCGCGGTCAGCAGCTCCCCGCCCCACCCCTTCGTGCGGTCGACGTTCTCACCGAACTTCTCGGACAACCGAGCCAACTGCTCGTGCATCCTGGACTGCGCGGCCACCAGGTCCACCGAGCCGCCCGAGAGCGCGTCGAGCGCGTTCTTGAGCGCGCGGGCCTTGTCGTCGGCGCTGCCGGTCTCGTCGGCCAGGACGCCCATCGCGGCGGCGAATTCCCTACCGGACGCCGTGCCGTCGACCATCGATGCCCGGCCCTCGCGTAGCGCCTGGTCGAGGTCGCGTTGCTTCTGGTCAGCCTCCTGGTACTGCCGGGCCAGCCCGTCGATCTCACCGAGCAGGTCTTGTGCCGCTTTTCCTTGCTCTGTAAGACTTTTCGTCTCACTGACGACACCGGATTTCCATCCGGTGCTGTTAGTCACCCAGCGGGTCTGCTCCTGAATGATCGAGTTCAACCGGCCGCGCACCCCGTCGAGCGCGTCCGAGTTGCCGAGGGTGGCCTCGGTCAGATCGGACAGGCTGATCCCCGCCGCGCGGGCCGCGTCAGCGACCGTCCGCCCGGACTCGGCGACCTTCTCGGACTGGAGCTGCTGCGCCTGGTGCGCGCGCACCGACTCGGTGATGCGCCCGGAGGACTCGCTCAGCGCAGCCGCGAGCGCGTCCACCGCCGAGCTGTGCTGCCGAGCCCGTTCCGCCGCCGCTTCCTGGCGGCCGGATAGCAGGGACAGCCCCAGCGCCACACCGCCGATGGCCAGGCCCACCGGCCCACCGAGGGCGGACACCAGCGCACCGGTCCCCACCCGCAGCGCGGTGCCGCTGGCCGCAGCGACCCCCGCAGCCGTGCCGAACCGGGTCGCACCAACGGCGGCCTGCTCGAAGCTGCCCCGGACCGCTGCGAGCGCTGGCGAACGCTCGGCGAGCGTGCCCATCGCGGCGGACATGCGCCCGATGGGCTCGCCGGTGGCGGCGGCGCCCGCGCGGATAGCGGCGGTCTGATCGGTGAACGCGCGCGCGCTCTCCACCGCGGGCACGGTGCTGGTGCGGTAGGCGGCCATCGCGGCACCGAGCTTGCCAACCTCCTGGCCGCCGCTCTGCGCGAGAGCCTGCTGGGTGCGCATCTCGCCGCTGAACTGCCGCAGACCGGACAGCACGGTGCTGTCGCCGAGGCGCCCCTGCGCGAGACGGAACGCGCCCAACGCGAGGATGCCGGTCTGCACCGGGCCCGGCAGGTCGTTGAACAGCCCCAGCACAGTGCTCAGTGCCTTGCCCACGGGCACCAGGACGCCCGACAGCGCCTCGACGGCGCCCCCGAGCACCCCGACCACGGTGGACAGGGTGCCGACCACGCCGGTGCCCTCGCCCGATGCGGTGGCCAGCTCGCCTACCTCGCGGGCCACCGGGCGGGCGGCCTGCACGGTGGTGTCCAGCACGCCGGTGAAGTCGTTCCACAGCTCGATGCCGGTGTTCACCGAGGTGTTGAGCGGTTCGAGCGCGCCGGTGCCCAGCGGCCCCAGCACGTCGGACACCGCAGCACCGACGACGTCGGCGCGGGCCTCGATCGCCGCAGCCAACCGAGGTCCGTACAGCTCCCCGGCCGCGACCGTGGTTTCCAGCCGCGAGGCCACCGCCGGGCCCAACTGGTCAAGGCGCGTCGCGGTCGCGCGCACCACGCGCTCCAGCGGTTCGTCAACCGCGTCGTAGATCCCGATCGCAGCGGACTCCAGCTGCGACTGCAACGCGTCCATCGCGCCGCCGAGCCCGGCCGTCTTGGCGGCGGCGACGTCGGCCGCACCGCCCTGCCTACCAACGGCTTCCGCCATGTCATCGAACGCGGTGGCACCGCTGGCCGCGAGTGATGCCGCCACGGTCATGCCCTCGGTGCCGAACGCGGTCGCGGCGGCTGCGGCGAACGACTCCTGCGTCATGCGCTGCTGCGCCTCGGACAGCTGTTCGGTGATCGAGCGCAACCCGACGAACCGACCGGTGGCGTCGAACGCGGTGATACCCAACTCGCCCAGTGCCTTGGACGCGGGGCCGCTCGGGGCGGCGAGACTGGCCAGCATCCCCCGCAGGGACGTACCGGCCTGCTCCCCTCGAATGCCTTGCGTGGCAACGACACCGATAGCCGAGGCCACCTCGTCGATCGACACCCCGACGGACTGCGCCACCGGCCCGACGTACTGGAGGGCGTTCGCCACGTCCATGATCTCGCCGGATGCGGCATTCGCCACGTTGGCCAGCACGTCGGCGACGTGGCTCGCCTGGTCGGCGGCCAAGCCGAATTGGTTCAGTGCGTCGGACTGCACGCCTGCGGCTTCTGCGGCCTCGACCTGCGCGGCGGCGGCCAGTTGCAGAGTGCCGCGCGCGGCGGTCATCGCCTGGTCGATGTCCAGTCCGCCCTTGGCCAGTTCCCGCATGGCGCTGGCGGCGTCGGCGGCGCTGGTCGCCGGGAGCGTGAGGTCGGAGCCGAGTTCGTTGGCCACTTCGGACACGCGGGCCATCTCGAACCCGGTGGCCTCGCTCACCGCGCTGATCTCGTTCAGGGCACCGGTGTACTCGTTGCCGAGCTGGATCGCCTCGGTGAACCCCTTGGCGGCCAGCGCGGTACCTCCCACGATGGCCAGGCCGAGGGTCTTCATGCCACCGGAGACCCGGCTTGCGGACTGGTTCAGGCCGGTGTCGAGGTCTCGTTGCCAGGTGCCGAAATCGGGGCGAATCAGGATGTCGAGCGCGCCGCCGGGCATCGTCACCTCCCCGCGGTGTGCCGTCCTACTGCTGCCGGAGACGACCCGCGAACACGGCGGCCAGGGTGTCGAACCCGTCGGACCCGAGGCCGCCGTCCTGCCCCGTGGTCTCCGGTTCGACGGCGGTGGCGCCGAGTCCAGCAAGGCGCTCGGTGTAGGCGCGGAGCAGTTGCTCGCCGATCGCGGCCGGACGCAGTGCCACCGGGACCACAGGTGCGTGCCTGGGGGGCCGTCGCCCGGCCGTGCGTGCGCGGGCTGCCTTGACTTCGGGGTCGTCCGGGTCAGTGACGCGGTCCGTCCACGCGGTCTCGGCGAGATGGCTGGCCACGTCGACCAGCTGCGCCACGTTCTCCTCCAACAGGCTCCACGCGCCCTCTTGGCGGGCGAGCGCGCTTTCTGGTGGGAGCCCGCGCACGCACGCCAGGAAGTCGGCGACAGGCAGCGTGCTCCAGGCGTTCCGCAGCGACCAGGGGTAGTACCGGGCGAAATCGGCGGTCAGGGCGTCCCACCACGGTCCGAGGACCGTCAGGAGGACGCCGAGCGTCCCCCCTGTTCGTCGACCCCCTCGGCTGCGTCCTGGTCCTCGTCGGCAGGGGTGCGGGTGAGTACCCCGGCGGTGCGCATGATCCGCGCCAAGATCACGTTCATGTGCTCGCGCGGGAGCACGTCGAGCTGGGCGTTTAGCTGCTCGGCGAGCGCGGGTTCGGTGAGCAGCATGGCCAGTGATGCGGCGTCCTGACCCTTGGAGACGGTGTGCCAGTACTCGACGTACTCCTCGGGGGTCAGGTCGCGCCGCACGGCGAAGTCGAGCCCGAACAGCCGCTTGGGTGCCGGGGTGAGCTGGCGGGCGACGACGAGCGCGCCCAGGTCCTCCACATCGGCAGGCTGGGCGCTCTTGCGGGTCGCGGGCATGGCTTTCTCCTTGTTCTGCAATGGTTTCGTGGTCATGCCGCGAGGGGGTTCCAGTTGCTCAGCGGTACTACGGCCTCGGACTCGATGGACGGTGCGAGACAGGTGATCTCGAATTCCCAACCGTCGAGGTCGTCGTCGTTCTTGATCTCTTCGGGGTCCTGGGAGAGTTTCGCCCGTTCGATCCAGAACGCCATCTTGCGACCGCCGGGGCCGCGCAGCTGGAGCAGCAGGGAGAACTCGTCACCCTCGGTGCCACGGTTCCACCGCCACTGACCGGCACCTGCGGTCGTCTCGGTGATGCTGCCGCCGCGCAGCTTGGTGAGGATGGCCGCCTTGGAGTACTGCGAGACGCGGAACCGGATTCGGGTGGTGGTCTGCCCCTCGTGCTCGAAGAACGGGCCCCCGGATTCGTTGTTCCACACGTCGTACGACTTGACGTCCTGGGTGGGGGTGATGTTGAAACCGGCTTTGACGCCGCCGAATGCGGACATCGCGGCCGGGGTGGTGTCGCCGGTGGTCGGGCTGTTGCCGAAGACATCGGCGGGGATGACCGCCCCGCCTGGTCCCCGCCAGGCGTCGCCGTCGACCCACAGCACCGCCTGCGCGGCGTTGGCCTGGGACATGGGATCTCCTGCACTCCCGCACTATGCGGGGCTGAAAGCGTTGTGCTGTAAGGAAAATCAGGTCATTCGTGGAGTTGCAGGCGCAGCTCGGCACGCACGAAAGCGCCGTACAGGGGTGTGCCCGCGCCGCGGGTGGTGTCTGGTGCGTGCGGCTGCGGCCCGTCGACCAGGCGCAGGGAGTAGGTGACGGTCCGCCAGGTGCTCGCGCGCACGGCACCGAGCACGCGGGCTGCCTCAGCCGCGATCGCCCACGCCTGCCCCTCGGGGTCGGCGGTGCTGCTCGGTGGAGCCCACCCGGACACCTGCACCAGCGGGGCGAACGCGATTCCGTGGCCGTCGATCGAGGCGACGGAGGGGACCTGCACGCGGGCGAACGGTCCGCGCAGCGGGTCCGGTGTCCGGGGACCGATGCCCGCAGGCGCGGACTGGACGAACACCGGGTCGGCCCGCAGGTGCGCGAGGACCGCACCGGCCAACCAGGGCAGCACCAAGGGCACGCCGGGATCACCGCCTCGGCCTGGTGCCGCGGTACCTGCCGTGGCGGCGAGCGGCGTCGGTCAATGTCGCCTGCGCCTCGCTGTCCGCGGTCCCGTATTCCTTGAACGCGCCGAGCGGGTCGGTGTCGACGACGCGGACGTGATCACCGTCGGCCACCACGCCGATGCCGTCGCGGAACGCACCGGTGAGCACGCGCGCGGTGTCGCGGGCTTCCTCCGCGATCGTCGAGGCGATGGTGACGCGGCCGTCGTAGGACGCGGTCAGAGCCTCACGGACGGACTGCTCCGGGTAGACGGTGACGCGGGCGCTCACGGTCACGGGGGCACCTCCTGCATGTCGGAGATCAGCACCAAGGCCGCAGCAAGGAAGCCGCCCCGGTCGCCGGGGGCGCTGTCCACCACGTAGCGCGTGCCGGTGGTGAGGTCGAGCACCGTGGCGCCAGCGACGAGCACACCGGACAACGCGCGCTCGAACAGCGCGCCGTGGTCGGTGACCCGCACAGCCGCGGTGGTGGTCGCGTTGCCGCTGACGGTCGTCGAGCGGCGCCAGATCGCGGCCCACCCGGTCGAGATGACCGGAGCCAGGTGTACCGGCTCACCGGTGACCGGATCAGGGATCGGCGACACCGGGCCCGGACGGCTCACGCGCACCTCGCGGTCCAGTCGTGGCCTGCCCATCGGGCACCCCCTCCCCGTCGATCAGGTGCGCCGTCCCTGCGGCCAGGGCGGCGACGACCCAGGGCGCCCACCGCGAGGCGTGGTGGACCCGCCCTGCGCCGTCGCGGACCCGCACGACTTCGTGTACCGGCTGTACCGGTGCGGTGGTGCGCTTCGTGGTCACCGCGGGTCTCCGATCGGCGGGTGCGCGCCGTTGTGGACCAGTTCGTAAACCCCCGCCTCGGGGATCATCGGCGTGAGGCTGCGGAGCTGGTCGAGCTGGTCGAGGCTGAACATGCCGCCGCCGCTGGCGCGCTCCTGCTCGTAGCTGTACTCGCCGCCGTACTGCTCGGCGGTCTTGCCGGGGGTCAGGCCCATGCGGACCAGCACTGCCCAGCAGACGACGCCACCGGCGACGCGGAGCACGTCCGGGTCGTCGGTGGTGACCAGGACCGGGGCAACGCGGCGGGCCTCGGCCAGCGCGTCGGCGAGCAGCGCGGCGACGCGGTCCTCGTCGCCAGGCAGCACGGTGCCGGTCGGCGCGCGGTCGCGCACATCCTGCACGGTCAGGGTCAGCATGGGGCCCTCCCCGTCAGTCCGTCACCGGCGTGGCGGTTGTCGTGCCTGCGGTCAGGTCGTGGGTGACGGTGACCCGCTGGCCGTCCGGTCGAACGCGCTGGTACGTCTCGATCCTCGATGGAGCGCTCGGCGCCTGCGCGTCCGTGCGTCCCACCGGGATCACCGCGTTGACCATGCCGTGTCCGGCCAAGGCCGCCGCCGCCTTGTCCGGCACGGCGGAGACGGCGACCTCGGCGGGGTCGGTGGTGTCCGCGGGGCCGTCACCGGTCGCGGTCACGGACGGCCGGTCCAAGTGACTGTCCAGGGTGGTCTGATTGCTGGTCTTGCGGGCAGCCACTGGGCTACCTCCTTTCGTCACCGGGACAGCACGCCGCGCAGCCGCGCAGCCGCGCGACCGCCGAAGGTCGCCATCCCGCAGAAGAACTCGATGCGGGTCCGGTACGCGGGCTTGTCGTCGACCTCGCCAAGGTCGCGCACGTCCACCCCGCCGTTGGTCAGGCCCGTCACGGCCTCATCGCTCTCGTCCTGGCCGAACTTCACCGCGTAGACGGAGCTGGTGTTGGTGGCGGTGCCCATCGTCTCGTTCTGCGGCAGGATGTCCGTGCCAGCTCTCGTGGTGCCGGGGTCCAGGATCGGCACCCCGTTCCACGTGGCCACGCGCTTGCCGGTCATGTCCTCCTTGACCATCTCCACGCCGCCGAGCCGGCGACCCGCGCTCTTGATCTTGGCGATCACCGCCGCGTTGGCGTACGCCACGTCCGGCCCACCGCGAACAGCCGCGAACAGCGCTTCCAGTTGGTCGAAGAAGTCCTGTGCGTCCGAGCCGCCGTTGCCGACCACGGGCAGACCGTTGGTTCCCGCATCGATGACCTGAGGGCCGGTGAGCCGCTTCCGGAGCCCGTCGAACCCCTTCGGGTCAACGACCACGTCGCCGTTGAAGAAGTAATCCTGGAACTTGTAGGAGGCGGACTTGACCTTGGCGCGGGTCTGCTGCGCGCGCTGGTCGGTGAGGTTGCTGCGGGTCCGCTGGATGAAGGTGTCCACGTCGGCGTCACCGCCGAGGATCGCCAGGGACTCGCTGGCCTGCACGAAGGTACCGGTGGACTCGGTGTACGCCTCGTTCACGCCGCGGAACGCCACGTCCGGCAGCGTCCCCTCCTTGTTGTAGGAGTAGGCGTTGCCCTCGATCTGCATCAGCGGAAGCCGGTCCAGAATCGGGGATTCCTGCACGAACACTTCCATCACGCCGCGCGCCAACTGGTTCTGTGAGAGCACGGCGGCCTGGGCAAGAGTCACTGCCATGACGGGGTTTCCGTCCTTTCTGGATGCCCCTCGGCGGCAGCGGCCGACCAGGGCGGGGGAATCGGGCTACTTCTTCGCTCCGGCCGCGTAGGCGGCGCTGAGCCGACCCAGTCCGGGGGCGACGGGCGCGCCTGAGGTGGTGCCCCCGGCGCCGATACCCGCGTCCGCCGGGGACGCGGTCCCAGTGGTGCTCTGCTTGAGCAGGTAGGGCTTTGCCTTGGCCAGCTCGTCGACGAGCTGCTTCACAGCGGCCTGGTCGACCTCACCGGTGTCGGTGACCTTTACCGCGGACAACTGCTCGCGCAGTGCAGCCAGGGCGTCGCCGGGGTCGGCGAACCCGCCCGATGCGGCTGCGATGCGCACCTCGGCGGAGACCAGGCGGGCGTTCGCCGCCGTGGTCGCAGTGTTGGCACCCTCCCGGCGGGCGGCGTCGAGAGCCTTCTCCTCGGCGCTCTTGTTCGCGTCGCGGAGCTGCTGCAACTCGGCTTCGAGCGCGGCGGCGCGCTTCTCTGCGGCACCGCGCTGCTTGCGCTCTTCGGTGAGCGCCTTCTTGCCGGCATCACCGAGCTGATCGTCGGCCGTCGGTGCCGGGGCGGGCTGCGTGCCGGCACCGCCACCACCGGTGGTGCCGTTGGGCTCGCCGCCCTGCGGGGCCGTGCGCAGGTAACGGGACATGGTCCGGCCGTTGGTGCGGTACATCGGGGGTCCCCTCGGGGGTCGGGCCCCGGCATCGCGCTCAGGGCCGGTGAGAGCCGGACCCGTCGCGGGTCACAGCAGGTAGCCGAACCGCCGGAGCAGCCGCAGTGCGTGCTCCCGGTCGTCGGCCAGTTCGTAGATCGATTCGGGCATCAGGCGCGGCGTGGTGGCGCGCCGGTAGCGGTCGCCGAGCAGCCGCGCCAAGCCCTCGGCGGCAAGCCGCTGTCCGGCCAGGCCGCGCACGGTGGTGCCCTCGGTGGTGACGTAGACCTCGCGGCCGTCCACGGTGACCGGCCGCAGGCGTCCGGCCGCGCGTCCCTCGCGGAGCGCGGCAGCCTCCTCCGGCGTGATCCGGGAACCGGCGCCCGCCAGCCCATACGCGCCCTGCCGGGCGTTGACCACCTGGCCGATGTCGGCCCCGTCCCGGATGGCCTGCGCGCCCGCGCTCGTGAACACCCGATCCTGTTCGGACTCGCTCAGGGCGTCGAAATACTGCCGGGGCGAGGTGGTCAAGTCCGGGGCGCTCTCCGCCGCGGGGATGTGCCGGCAGTCGCAGCGGTGGTGACGACGGAACGCCGTCCGGCGTCCGTAGACCCGGCCCGCCAGCACGGCGCATCGCGCGCACGTGGGCGGTACCAGCATCCGCACGTAACCGCGGGTGCGCGGCGACGCGATCCCGGCAACCCCCTCGGCCTGCCGTCCCGCGTCGGCCACCGCGGTCGACACCAGCGTCACGACCGTGAGCTGTGCGCGACGCTGCGCCTCGGCGAGCGGCAACCCCGCGTCGAGCGCTCTGGCGCGCACCGACACCGGCGCCAGGATCAACGTGTCCAGCAGCGATAGCGCCGAGTCGACCAGCCCGCCGAACGCCTCGGCGGGCACCTCGCCGTCGAACGCCGCCTCGACCCCCTGCGCGGTCAGCGCGGCGCCCACGTAGTCCTGCGCACCACCAGCCGCTGCGGTCTGCGCGATCATGACCGCCTCGGCCAGCACCGCCGCCACGTCGGGCCACGACGCCGAGCCGTCCACCCACGCGCGCTCGGCGAGGTCGGTGGCGCGGTAGACCAGGCCCTGTTGCCGCCGGTAGTGCTCGGTGCCCAGCGCAAGCAGTTCCCCGCCGAGCCCCATCACGCCGCCACGGGCTCGCCGGGCTGCTGGAACTTCGGCATGGTCAGCACCGAGGCCAGGTCACCGCCCGCCAGGCGGGCTGCTGCGGCGGCCTGGTGCTGCGTGAACTGCGAACGCCAGCGCTCCTGGTCCTGCGGGGTAGCACCGGGGATCATCTCCCGCCCGGACTCGGGCGCGAGTACCGGACCGCCCACCAACTTGGTGATCGCATCGACCACCTGACCGATGCTCACGCTCTCCGTCTTGCGCCACATCGCCTGCGTGGCAAAGGGTTTCGTTCCCGAACCGGCCAACAGCGCGGCCTTGCCCATGACCTCCTCCCACGCCGCGGCGTCGGTGGTGCACGCCGCCGCAACCTTGCGCGTGAGCGTGGTCTCGGCGGCGGTCAACGCCTCGGCGCTCAGGTTCGACAGCTGACCGAGCAGGTAGTGCGGCGGGGTCTGCGACGTCGCCGAGAGGTGCTGCACGTGCGACGACATGGCGTCGGCGTACGCCCTGAGATCGGACTCGCTGAACTCGAAGATTTTCGTATCAGCACCGGGGAAAACCCATGTCCGATCGACGCCCGCGCGCGGCACCGGCGACATCAACGGTTTGGGCTGTCCGGTGTGCGGGTCGATGATCGGGCGCCCCTCGGCGTCGACCTGCGGGATGGGCCTGCCCTCGGCGTCGCGCATCAGCGGGTCGAAACCAATCACGCCGCGCTGCCGGAAAGCGGCGAACTGCATGGCCAACATCAGGTTGAATCGCGTCGTGTTGATGCTGTCCTGCAACGGGATCAAGCGCTCGATTTCCGAGTAGCAGCGTCCCTCGGAGTCCTGGTCGTTGGGGAAGGCGACGAACGGGATGCCGTGCGGGTGCGTGCCGCTGGCGACCAGTGTCCAGCCACCGCCGAGCCACCCGGCGCCGCCCGCCATCGCTGTTCGGCGGTACCGAATCCAGCTGGTCTCGTCGTAGACCACCGCGTGCTCTACGTCCGTCCACTGCGGCTGACCGGTCGTCCGACTCGGGGTCTTGGTGGTCCAGTTCTTGACTGCCCACCCGATGCGGAACGGGTTGTCGTCGTGCGGGAACAGGAAGACCCGGCGCGGCGACTCCGGTGTGATCAGCGGCAGGGCACCCTGCTGCGGCCACACCGACACGATGCCCTGTCCGTACACCATGCGGTCGCTGTAGACCATCGACTGACGGCCATGGAGCTGGTTCGTGCGCCAGATTTCCCACGTGGCCGCGTCAGCTTCCTCGTCCGGGCGGCCGTCGGCGTTGGTGCGGAACCCGTCGACGGCCTGGCGCTGCACGGCGGCCTTCTCGACCAGGTCCAGCCACGGCGCCATGCTCATTTCGCGCAGCCGCAGGTACTCGTTGCTGACGCCGTCGGGCGCGTAGGGGCGGTCCTGCCCGGTGCCGGTGGCGTACCCCTTCCAGCGGTCCAGGTCCGGTCTGCGCTGCCTAAGCTCGTAGAGGCCCAGTTCCCTGCACTCGGCTGCGGTACGGGGGTCCAAGCGTCACCCCCGATCGTCAGTTGAATCCGTAGTAGACGGTCGAGATGTGCCGCTGTTTGACCGGTGCGGCGGTGAGGACGTCGGCGCGCGCCTGGTAGGCCAGCGCGCCGCCCATCAAGGCGTCGATCTTGCGGTTCGAGCGCGGGGTCTCCTTGCGGATCAGCCTCATGCCGCGGGCCCTTCTGACGTAGGCGTTGCCGACGTGCTCGGCCATCGTCGTGTCGCCGTCGTTGGGCACCAGGCCCGCGATCAGGTCGGCGCGCAGCCGGTCCAGAGCCTCACCGGCGCGCTTGTCGCCGTTGGTCTCGTAGGCGCGGACGCGCTGCTCCTGGCCGCCGTAGAGCTTGACCCACGTCTCGATGTCGCTGCGCCACTCGTGCGGGTCGCAGTACATCAGCCGCACCCGGTAGGTGCGGAACGCAGCGGCGACGCGCTCGTTCACCTCGCCGCGCGGCACCGACCAGTGCGCGCCGCGCGGCCCGTCGGGCTTGGCCCAGATCCCCAGCACGAACAGCAGGCCGTCGGACAGCCTGCACCCGATGAGGACGGTCGCGTCGTCATTGATCGAACCGTCGAACCCGACGGTGATCTCGTCACCGGGTGCGAGCGGGTGGGCCTGCGCGCCGAGCCGGGTCCCGCACTCCCAGTGCTGCGGGTCGATCCACGTGTCCGAGGCAACCGAACCCCGGTTCAGGAAGTACCGTTCGGCGTCCGCAGGGTCCTGCTGGCGCAGCATCTTGCGGTAGATGCGTTCGGGATCAAGGAAGTGCGCTTTGCCGCGGGCCTGGCGGATCTGCCGGAGCGTGTGCTCCTTGTCCGCCAGGTCGAACTTCCCGCTGGCCTGCCGGTGGTTGACGTACAGCCCCAGCTCGGCGCCGCGCTCCTTGTACTCCCGGAACGTCGTTTCCGCGACGGACAGCTCACCGCGCCGGTACATCGTGGTCGTCTGGAGCAACCAAGGCTCGGCAAGTCCGCGCTTGGCCAGGTTCCGGGAGACCGTCTCGTACATGGCGATCAGTTCGCGCAGGATGTACAGGTGCGTCTCGTCGGCGACGACGAAGCTTTCCTTGCCGCCGTCCTTGGAAGCGGAACCCGTTGTGCAGTAAAGGATTTTGCCGCCGCCCGCATCCTCGTCGAAGTCCGCGAACTCGTCGGCCAGGGCGCCGTCGTCGGTGGGCAGCAGGATGCGCGTAGAGGTCTTCCAGTCCCGGCCGTAGTCCACGCCCTCGAACACCGGGTTCCCGCGGGTCCTGCCGACGTGGACGATGTAGGCGACGACCGCGTACGTGTTCTCCGCAGCCTGCCCCTCTTCGGTGGCCAGGATCTTGATCAGGGGCGAGCGGACGCGCCGCCCGACCGGTTGGCCGCTCTCGTCCCAATGGGAAAACCGGACGGCCGCGAACGCCTCGGCAAGCACGATCCACGCCGCCAGCTCGCTTTTCGCCCACCCCTTCATCCGGGAGATGACGGCCTCGTCGTAGAGCCGCTTTCCGGTGGTCGGGTCCAGTTCGTAGACGTCGACCAGGAAGTCCAAGCGTTCATCGTCGAGCTGGACCGGACGGCCTTGGACGTCACCGGGGCCGTGGACGCAGTTCGCCTCGATCCATGCCGCGATCTCGTAGCCGAGCGAGCACTTGTGCCCCTCGAACAGCGGGCCCGACCACCCCACGGGGATCACCTCCCCGCAGCGCGCCACCGCCCGCGCTGGTGCCGTACCGGCCCGCAAATCGGCCTATTTCTGTTGCCAGGTAAGGGATAGCGTCTGCTCTATGGCGGTTGACGTGCACGTGATGGGAGAAGGCGGGGCAGCGAGGCGCCTGGTCGCCGCGCTCGGTGAGTCGCTGGAGCTGGCGATGCGCTCGCGCAGCGCCGGAATGAGGAACCGGTCCGACGGCGTGCGACTGTTCGGCCAGGCCCGCCCGCACGCGAACGAACCCGTGGCGGAGTTGGCGGTACCCGAGCTAGCCGCGGCATTCACTCTGGTACCGGACCAGGGCGGGCGGGTGCGGCTGAAACTGACCGGGGAGGAGCCCGAGCTGCGGGCTGTCCTCACGGCGCTGCGCCCGCTGTTGAGCCTGCTGGTCTACCCGGCCGAGGCATACCGGGCGGACGGCATTCTCGGGTGGGCGGTCTACCTGCACGTCGAGACGACCACCTTGCCCGAGCCCACCGGTCCGGTCGCGGACACCGTCCCCGAGCAGCCCCGCGGTTCTCGGTGGGCACCGTCGGAGCGCGCCGACCGGCGCCCGGTCACCGGGCGCCGCGCGCTGCCCCGCGGGCGCCGGTGAACCCGACCGTCGAGACTTAGGCGCCTGCGCTGCGCCGCCGAGCCCGTTCCAGCGGTGACACCGTCCCGCCAACGGCGACCGTCCCGGACGGCTGGTATGCGCCTCGTGCCCCTCGGAGCTGAGGACGCTTCCCGGTCTTGGTGTCCGGCAGGCGCAACGTGACGAGCAGTTGCTTGAGCACGTTCTGCTGTTGCCGGGCCTCGGACAGCGCACCGTCAACGACCAGGTGGAACGTGGTGTCGTCCTCACGGTCTTCCCGCACGTGCACCATGCGCGCGCCCGCGCCGGATAGCTGGCGGTCCAGCTCGTCGAGCCGGTCGACGATCCGGCACGCCTCCCGGACCAGGATGGTCTGCGCCGGATCGAACGCGGTCAGCTCGTGCAGGTCGCGCCACAGCGCGGCACCCGCCTGGTCCAGCCCGGCGGGCGGCTGCGGGGTGTCCACGTCGTCGGCCAT

Protein sequences of DBSCAN-SWA_1

>NZ_CP023445|5933194:5947561|5946585_5947104_+|WP_096495976.1|DBSCAN-SWA
MAVDVHVMGEGGAARRLVAALGESLELAMRSRSAGMRNRSDGVRLFGQARPHANEPVAELAVPELAAAFTLVPDQGGRVRLKLTGEEPELRAVLTALRPLLSLLVYPAEAYRADGILGWAVYLHVETTTLPEPTGPVADTVPEQPRGSRWAPSERADRRPVTGRRALPRGRR
>NZ_CP023445|5933194:5947561|5938959_5939265_-|WP_096497989.1|DBSCAN-SWA
MSARVTVYPEQSVREALTASYDGRVTIASTIAEEARDTARVLTGAFRDGIGVVADGDHVRVVDTDPLGAFKEYGTADSEAQATLTDAARRHGRYRGTRPRR
>NZ_CP023445|5933194:5947561|5941556_5942189_-|WP_096495972.1|DBSCAN-SWA
MYRTNGRTMSRYLRTAPQGGEPNGTTGGGGAGTQPAPAPTADDQLGDAGKKALTEERKQRGAAEKRAAALEAELQQLRDANKSAEEKALDAARREGANTATTAANARLVSAEVRIAAASGGFADPGDALAALREQLSAVKVTDTGEVDQAAVKQLVDELAKAKPYLLKQSTTGTASPADAGIGAGGTTSGAPVAPGLGRLSAAYAAGAKK
>NZ_CP023445|5933194:5947561|5940542_5941490_-|WP_096495971.1|DBSCAN-SWA
MAVTLAQAAVLSQNQLARGVMEVFVQESPILDRLPLMQIEGNAYSYNKEGTLPDVAFRGVNEAYTESTGTFVQASESLAILGGDADVDTFIQRTRSNLTDQRAQQTRAKVKSASYKFQDYFFNGDVVVDPKGFDGLRKRLTGPQVIDAGTNGLPVVGNGGSDAQDFFDQLEALFAAVRGGPDVAYANAAVIAKIKSAGRRLGGVEMVKEDMTGKRVATWNGVPILDPGTTRAGTDILPQNETMGTATNTSSVYAVKFGQDESDEAVTGLTNGGVDVRDLGEVDDKPAYRTRIEFFCGMATFGGRAAARLRGVLSR
>NZ_CP023445|5933194:5947561|5943313_5944816_-|WP_096495974.1|portal|DBSCAN-SWA
MDPRTAAECRELGLYELRQRRPDLDRWKGYATGTGQDRPYAPDGVSNEYLRLREMSMAPWLDLVEKAAVQRQAVDGFRTNADGRPDEEADAATWEIWRTNQLHGRQSMVYSDRMVYGQGIVSVWPQQGALPLITPESPRRVFLFPHDDNPFRIGWAVKNWTTKTPSRTTGQPQWTDVEHAVVYDETSWIRYRRTAMAGGAGWLGGGWTLVASGTHPHGIPFVAFPNDQDSEGRCYSEIERLIPLQDSINTTRFNLMLAMQFAAFRQRGVIGFDPLMRDAEGRPIPQVDAEGRPIIDPHTGQPKPLMSPVPRAGVDRTWVFPGADTKIFEFSESDLRAYADAMSSHVQHLSATSQTPPHYLLGQLSNLSAEALTAAETTLTRKVAAACTTDAAAWEEVMGKAALLAGSGTKPFATQAMWRKTESVSIGQVVDAITKLVGGPVLAPESGREMIPGATPQDQERWRSQFTQHQAAAAARLAGGDLASVLTMPKFQQPGEPVAA
>NZ_CP023445|5933194:5947561|5937864_5938455_-|WP_096495966.1|DBSCAN-SWA
MSQANAAQAVLWVDGDAWRGPGGAVIPADVFGNSPTTGDTTPAAMSAFGGVKAGFNITPTQDVKSYDVWNNESGGPFFEHEGQTTTRIRFRVSQYSKAAILTKLRGGSITETTAGAGQWRWNRGTEGDEFSLLLQLRGPGGRKMAFWIERAKLSQDPEEIKNDDDLDGWEFEITCLAPSIESEAVVPLSNWNPLAA
>NZ_CP023445|5933194:5947561|5937445_5937868_-|WP_157767846.1|DBSCAN-SWA
MTTKPLQNKEKAMPATRKSAQPADVEDLGALVVARQLTPAPKRLFGLDFAVRRDLTPEEYVEYWHTVSKGQDAASLAMLLTEPALAEQLNAQLDVLPREHMNVILARIMRTAGVLTRTPADEDQDAAEGVDEQGGRSASS
>NZ_CP023445|5933194:5947561|5933194_5936926_-|WP_157767844.1|tail|DBSCAN-SWA
MTMPGGALDILIRPDFGTWQRDLDTGLNQSASRVSGGMKTLGLAIVGGTALAAKGFTEAIQLGNEYTGALNEISAVSEATGFEMARVSEVANELGSDLTLPATSAADAASAMRELAKGGLDIDQAMTAARGTLQLAAAAQVEAAEAAGVQSDALNQFGLAADQASHVADVLANVANAASGEIMDVANALQYVGPVAQSVGVSIDEVASAIGVVATQGIRGEQAGTSLRGMLASLAAPSGPASKALGELGITAFDATGRFVGLRSITEQLSEAQQRMTQESFAAAAATAFGTEGMTVAASLAASGATAFDDMAEAVGRQGGAADVAAAKTAGLGGAMDALQSQLESAAIGIYDAVDEPLERVVRATATRLDQLGPAVASRLETTVAAGELYGPRLAAAIEARADVVGAAVSDVLGPLGTGALEPLNTSVNTGIELWNDFTGVLDTTVQAARPVAREVGELATASGEGTGVVGTLSTVVGVLGGAVEALSGVLVPVGKALSTVLGLFNDLPGPVQTGILALGAFRLAQGRLGDSTVLSGLRQFSGEMRTQQALAQSGGQEVGKLGAAMAAYRTSTVPAVESARAFTDQTAAIRAGAAATGEPIGRMSAAMGTLAERSPALAAVRGSFEQAAVGATRFGTAAGVAAASGTALRVGTGALVSALGGPVGLAIGGVALGLSLLSGRQEAAAERARQHSSAVDALAAALSESSGRITESVRAHQAQQLQSEKVAESGRTVADAARAAGISLSDLTEATLGNSDALDGVRGRLNSIIQEQTRWVTNSTGWKSGVVSETKSLTEQGKAAQDLLGEIDGLARQYQEADQKQRDLDQALREGRASMVDGTASGREFAAAMGVLADETGSADDKARALKNALDALSGGSVDLVAAQSRMHEQLARLSEKFGENVDRTKGWGGELLTAQGRLDTTQENARGLHSVLTDLRDATADTALKTYELARAQGEDVTTALAKAGAEVASARDGFYAAAEAMGIGRAEAEALANQYGLLPSQVVTLIDAQDVDKTTLELQLLKWQAEQVPDRRSITVETLSDQAVERLRAVGLEVNNVPGGKEIVLRGNDSDFNQKIAAATAPATKYVTVIYTSGKSMPNGPMAVNHDGNLLAPSVVAYADGGIHPLTPMRGGWAQFVDPNTWRVIGDRMTHREAYIPVNGSTRSTGILAETARLMGYDLIRRFASGGLATPAASAPVPASAAATGVPVITNNISVQRNQDAHVMAAVISSTAAWQARTRR
>NZ_CP023445|5933194:5947561|5940201_5940525_-|WP_096495970.1|DBSCAN-SWA
MAARKTSNQTTLDSHLDRPSVTATGDGPADTTDPAEVAVSAVPDKAAAALAGHGMVNAVIPVGRTDAQAPSAPSRIETYQRVRPDGQRVTVTHDLTAGTTTATPVTD
>NZ_CP023445|5933194:5947561|5939789_5940188_-|WP_096495969.1|DBSCAN-SWA
MLTLTVQDVRDRAPTGTVLPGDEDRVAALLADALAEARRVAPVLVTTDDPDVLRVAGGVVCWAVLVRMGLTPGKTAEQYGGEYSYEQERASGGGMFSLDQLDQLRSLTPMIPEAGVYELVHNGAHPPIGDPR
>NZ_CP023445|5933194:5947561|5947120_5947561_-|WP_096495977.1|DBSCAN-SWA
MADDVDTPQPPAGLDQAGAALWRDLHELTAFDPAQTILVREACRIVDRLDELDRQLSGAGARMVHVREDREDDTTFHLVVDGALSEARQQQNVLKQLLVTLRLPDTKTGKRPQLRGARGAYQPSGTVAVGGTVSPLERARRRSAGA
>NZ_CP023445|5933194:5947561|5939267_5939630_-|WP_157767847.1|DBSCAN-SWA
MGRPRLDREVRVSRPGPVSPIPDPVTGEPVHLAPVISTGWAAIWRRSTTVSGNATTTAAVRVTDHGALFERALSGVLVAGATVLDLTTGTRYVVDSAPGDRGGFLAAALVLISDMQEVPP
>NZ_CP023445|5933194:5947561|5942258_5943314_-|WP_157767848.1|DBSCAN-SWA
MGLGGELLALGTEHYRRQQGLVYRATDLAERAWVDGSASWPDVAAVLAEAVMIAQTAAAGGAQDYVGAALTAQGVEAAFDGEVPAEAFGGLVDSALSLLDTLILAPVSVRARALDAGLPLAEAQRRAQLTVVTLVSTAVADAGRQAEGVAGIASPRTRGYVRMLVPPTCARCAVLAGRVYGRRTAFRRHHRCDCRHIPAAESAPDLTTSPRQYFDALSESEQDRVFTSAGAQAIRDGADIGQVVNARQGAYGLAGAGSRITPEEAAALREGRAAGRLRPVTVDGREVYVTTEGTTVRGLAGQRLAAEGLARLLGDRYRRATTPRLMPESIYELADDREHALRLLRRFGYLL
>NZ_CP023445|5933194:5947561|5938517_5938952_-|WP_096495967.1|DBSCAN-SWA
MPLVLPWLAGAVLAHLRADPVFVQSAPAGIGPRTPDPLRGPFARVQVPSVASIDGHGIAFAPLVQVSGWAPPSSTADPEGQAWAIAAEAARVLGAVRASTWRTVTYSLRLVDGPQPHAPDTTRGAGTPLYGAFVRAELRLQLHE
>NZ_CP023445|5933194:5947561|5936945_5937278_-|WP_157767845.1|DBSCAN-SWA
MEENVAQLVDVASHLAETAWTDRVTDPDDPEVKAARARTAGRRPPRHAPVVPVALRPAAIGEQLLRAYTERLAGLGATAVEPETTGQDGGLGSDGFDTLAAVFAGRLRQQ
>NZ_CP023445|5933194:5947561|5944832_5946485_-|WP_096495975.1|DBSCAN-SWA
MGWSGPLFEGHKCSLGYEIAAWIEANCVHGPGDVQGRPVQLDDERLDFLVDVYELDPTTGKRLYDEAVISRMKGWAKSELAAWIVLAEAFAAVRFSHWDESGQPVGRRVRSPLIKILATEEGQAAENTYAVVAYIVHVGRTRGNPVFEGVDYGRDWKTSTRILLPTDDGALADEFADFDEDAGGGKILYCTTGSASKDGGKESFVVADETHLYILRELIAMYETVSRNLAKRGLAEPWLLQTTTMYRRGELSVAETTFREYKERGAELGLYVNHRQASGKFDLADKEHTLRQIRQARGKAHFLDPERIYRKMLRQQDPADAERYFLNRGSVASDTWIDPQHWECGTRLGAQAHPLAPGDEITVGFDGSINDDATVLIGCRLSDGLLFVLGIWAKPDGPRGAHWSVPRGEVNERVAAAFRTYRVRLMYCDPHEWRSDIETWVKLYGGQEQRVRAYETNGDKRAGEALDRLRADLIAGLVPNDGDTTMAEHVGNAYVRRARGMRLIRKETPRSNRKIDALMGGALAYQARADVLTAAPVKQRHISTVYYGFN

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_157767844.1|5933194_5936926_-|tail	phage tail tape measure protein	A0A1C9EHW6	Gordonia_phage	2.9e-79	27.7
WP_157767845.1|5936945_5937278_-	hypothetical protein	NA	NA	NA	NA
WP_157767846.1|5937445_5937868_-	hypothetical protein	NA	NA	NA	NA
WP_096495966.1|5937864_5938455_-	hypothetical protein	A0A1C9EHX3	Gordonia_phage	1.7e-26	37.2
WP_096495967.1|5938517_5938952_-	hypothetical protein	NA	NA	NA	NA
WP_096497989.1|5938959_5939265_-	hypothetical protein	A0A1C9EHV8	Gordonia_phage	9.6e-13	43.7
WP_157767847.1|5939267_5939630_-	hypothetical protein	NA	NA	NA	NA
WP_096495969.1|5939789_5940188_-	hypothetical protein	NA	NA	NA	NA
WP_096495970.1|5940201_5940525_-	hypothetical protein	A0A1C9EHZ8	Gordonia_phage	8.6e-12	47.0
WP_096495971.1|5940542_5941490_-	hypothetical protein	A0A1C9EHV7	Gordonia_phage	1.0e-116	70.2
WP_096495972.1|5941556_5942189_-	hypothetical protein	NA	NA	NA	NA
WP_157767848.1|5942258_5943314_-	hypothetical protein	A0A2H5BLR1	Streptomyces_phage	6.0e-38	34.8
WP_096495974.1|5943313_5944816_-|portal	phage portal protein	A0A1C9EHZ9	Gordonia_phage	6.3e-65	36.4
WP_096495975.1|5944832_5946485_-	hypothetical protein	A0A1B3AY92	Gordonia_phage	4.3e-67	33.3
WP_096495976.1|5946585_5947104_+	hypothetical protein	NA	NA	NA	NA
WP_096495977.1|5947120_5947561_-	hypothetical protein	A0A173G9S3	Mycobacterium_phage	2.3e-07	36.9

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP023445|6738135:6789691|DBSCAN-SWA
GTCAGCCGCGCGCGACGGCCAGCACGTGCTGCACGGCCTCGTCGACCGGCACCTCGACGCGCTCGCCGGAGCGGCGGTCCTTGACCTCGACCAGGCCGCCGGCCAGGCCACGGCCGACCACGAGGATCGTCGGCACGCCCACCAGCTCGGCGTCGGCGAACTTCACGCCGGGGCTGGCCTTGCGGTCGTCCAGCAGGACGCTCAGGCCCGCCGAGGACAGCTCGCCCGCGAGCTTCTCGCCGCCCTCCAGGAGGGTGGCGTCCTTGCCCGCGACGACCACGTGCACGTCGGCGGGGGCGACGTTGCGCGGCCAGATCAGGCCGCGGTCGTCGTGGCTCTGCTCGGCGATCGCGGCGACCAGGCGGGACACCCCGATGCCGTAGGAGCCCATGGTGATGCGCACGGGCTTGCCGTCCGGGCCGAGGGCGTCGAGCGAGAACGCGTCGGCGTACTTGCGGCCGAGCTGGAAGATGTGGCCGATCTCGATGCCGCGCGCGGCCACCAGGACGCCCTTGCCGTCGGGCGACGGGTCGCCCTCGCGGACCTCGGCGACGTCGATCGTGCCGTCCGGGGTGAAGTCGCGACCGCAGAGCAGGTCGACCACGTGGTGCTCGTGCCGGTCGGCGCCGGTCACCCAGGCGGTGCCCTCGACGACGCGCGGGTCGACCAGGTAGCGGACCTTGTTCGCGAGCAGCGCGCCGGGACCGATGTAGCCCTTGACCAGGAAGGGGTGCGCCTTGAAGTCGGCCTCGTCCAGCATGGCGACCTCGGCGGGCTCGACGGCCGCCTCGAGGCGCTTGAGGTCGACCTCGCGGTCGCCGGGCAGGCCGATCGCCAGCAGCTCCCAGTCGGAGCCGGGGACGCGGGTCTTGACCAGCACGTTCTTCAGCGTGTCGGCGGCGGTGAACTCGCGGCCGAGGCCCGCGTTGTTGAAGAACTCGACCAGGGTGTCGATGGTCGGGGTCGCGGGCGTGCTGTGCACCTGCGCCTCGGGACGGCCCTCGACCGGCTGCGCGGGGGGCGCGGGGGTGGTGACGGCCTCGACGTTGGCCGCGTAGTCGGACTCGGTGCTGCGGACGAAGGTGTCCTCGCCGTTCGGGGCGACCGCGAGGAACTCCTCGGAGGCCGAGCCGCCCATCGCGCCGGAGGTCGCGGACACGATGACGTAGTCCATGCCGAGCCGGTCGAAGATCTTGATGTAGGCGGCGCGGTGGCGCTGGTAGGCCTCGGCCAGGCCCTCGTCGGTGAGGTCGAAGGAGTACGAGTCCTTCATGACGAACTCGCGACCGCGCAGGATGCCCGCGCGGGGGCGCGCCTCGTCGCGGTACTTGGTCTGGATCTGGTAGAGCGCGACCGGGTAGTCCTTGTACGAGCTGTACTCGCCCTTCACGGTGAGCGCGAACAGCTCCTCGTGGGTGGGGCCGAGCAGGTAGTCGGCGCCCTTGCGGTCCTTCAGGCGGAAGATGTTGGGGCCGTACTCGGTCCACCGGTTGGTGGCCTCGTAGGGCTCCTTCGGGAGCAGCGCGGGGAACTGGATCTCCTGCGCGCCGATCGCGTCCATCTCCTCGCGGACGACCCGCTCGATGTTGCGCAGCACCCTCAGGCCCAGCGGCAGCCACGAGTAGCCGCCCGGCGCGACGCGCCGCACGTAGCCCGCGCGGACCAGCAGCTTGTGGCTCGGGACTTCGGCGTCGGCCGGGTCCTCGCGCAGCGTGCGCAGGAACAGCGACGACATCCTCGTGATCACGGTTGGGACTCCTCGTGGGGCTGGTGGTCCTGAAAAGCCTAGTGAACGGGGTGGCGGGGGTTCCAGCCGGTTACCCCGGCGCGGGGCGGGCGGGGGTCCGCGGTCGTGACCCGGACGGGTGGTGTTCGGGGGTGGGGGCGGCGGTGGGGGTCGGGCGGGGCCGGGAATTGTCGGGGGTCGTCGTTAGCGTGCCGGGCATGGGGCTGAGCTACGGGATGACGACGGTGGACGCGGCGGACCCTCGGGGGTTGGCGGCGTTCTGGGCGGGCGCGCTGGAGACGGACGCGGTGCAGGAGTACGGGGACGACGGGGACCTGGTGATGCTGACGGCGGAGGGCGGGGTGCGGTTGGGGTTCCAGCGGGTGGCGGAGCCGACGCCGGGGAAGAACCGGGTGCACCTGGACTTCGGGGCGGCGGATCTGGCGGCGGAGGTCGAGCGGTTGACCGGGTTGGGTGCGGTGCTGGTGGCGGAGCGGTCGATGCCGGGGGTGGAGTGGGTGGTGCTGGCCGATCCGGCGGGGAACCAGTTCTGCGTGTCGAGGGCGGGGTGAGGTGGGGCGGGTGAGGTGAGGGGGGTGCGCGGCGGCGGTTGGTGACGCTTGGTGACCGGTCGGGGCGTGGTCGGGTCTCGGCCGGGGTGTCGCGTGGTCGGGTCCCGGCCGGGATGTCGCGTGGTCGGGTCCCGGCCGGGATGTCGCGTGGTCGGGTCCCGCCGGGGTGTCGCGTGGCCGGGTCCCGCCGGGGTGTCGCGTGTCCGGGGTAACGGCGGGAGTGGCGGGGACGGGCGGTTCCGGTGGGTAGGCTCGCCGGTCGTGCTCGTGCTGCTGCCTCCGTCCGAGACCAAGGCGACCGGTGGGTCCGGCGCTCCCCTCGACCTGGACGCGCTGTCCCACCGGGAGCTGAACCCGGTGCGCGACAAGCTCGTCACCGCGCTGGTCGACCTGGCCGCCGACGTGCCCGCGTCGCTGGCGGCCCTCGGCCTGTCCGAGCGGCAGGCCGGGGAGGTGGGGCGGAACGCCGAGCTGCGCACGTCGGCCACGACGCCCGCGCTGCGGCGGTACACCGGCGTCCTCTACGACGCGCTGGACGTCCCGTCGCTGACGAAGGCCGAGCGCGACCGCGCGTTCGCCAGGATCGGCGTGGTGTCGGCGCTGTTCGGCCTGGTCGGGGGCGGTGACGCGATCCCGGCGTACCGCCTGTCCGGCGGCAGCGCGCTGCCCGCGACCGGTCCGCTCGGCGCGCTGTGGCGCCCCGCGCTGACCCCGGTCCTGGCGGAGGCCGACGAGTTCGTCGTGGATCTGCGCTCGGGCCCGTACGCCTCCCTCGCGAAGGCCCCGGCCGCCGTGGTGGTGCGGGTGGTCAGCGACGACGGGTCCGGGCGGCGCAAGGCGGTGAGCCACTTCAACAAGGCCCACAAGGGCCTGCTCGCACGCGCACTGGTCCGCTCCCGCACCGAGCCGTCCACGGTGGCGGGGCTGGTGAAGGTCGCGGCGAGCGCCGGACTGACGCTGGAGGAGACCGGGGCGAAGGCCCTGGACCTCGTGATCATCGGCAACCCCGCGGACAAGCCTGCGGCCTGACAGCGGCACCGGGAACTCGGGCACCCGGAACTCGGGCACTCGGAACCTGGGAACCCCCAGAACTCAGGAGCTCGGAACCCGGGAACCCCAGAGCTCAGGGGCCCGGCAACCAGCCCCGGACTTGGCCCCGGCCCCGGCCCCGGACTTGGCATCGGCATCGGCATCGGCATCTAGCTGGCCAGATCCGGCGGCGGACTCTGCCCAGGCAAATCCGACAGGCACACGACAAGCCACGCCACCGGGCCGGGGCTTTACCGCGCTGGGACTCGCCGGGGCGGAGCGGGGGGCACCGACCTGGGTCGAACCGGGACAGATCGGGCCAGGCAGGCCGGGCAGGCCGGGCCGGGCGGGCAAGGCAGGCCGGGCCGGGCGGGCAAGGCAGGCCGAGCGGGGCGGGCTAGGGCAGGCCGGGCGGGCGAGCTGCGGCAGGGCGGGGCGGGGCGGGCTGGAGCAGGGGCGGGCAGGCAGGCGAGCTGCGGCAGGGCAGGGCGGCGGGGCAGGGCAGGGCGGCGGGGCAGGGCGGGCAGAACCGGGCCGGGCGGGGCAGAACCGGGCGGGGCGGGCGGGGCGCGTCTCGCCGGGGTTGGGTTCGAGCGGGCAGAGCCCGGTCGGGTCGTCGCCCTTGCCGCGCTTTGCCGCGCCCTTCCGCGAGGCCGCGTTCTCCGGCCCCGGCGCTCTCCCCCGCCGCCACACCCCAGCCCTCGCGCTCTTGCCGGGCGTTCGACGCGCCCCCGCCCCCTCCCCCACCGCTATTCCGGGGTCCCCAGCCCACGTCCGGTGGTGTCCAGCCTGCTCCCCGTGGTGTTCGGTGGGTTCCGGCGGTGTTCGGCGGTGTTCGGCGGTGTTCGGCGGGCAGGGTGCGCGCCGGCCCCGTTCGGTCGCCGCCGCTCGGGTGAACGGAGTTGCACGCTTCACGTGGAATGCCCGGATTCTGGGAACGGCGGGGGTGTCCGGGCCGACATCCGTCAGGGAGAGAAGTCGATCCGGGGGGTGTGCGTTGACCGGTGCTGATCCGGTGTGGCCGAGCACGAGTCTGCTGGGGAGGGTGCGCGAACCCGCGCGAACCGACCTGCTCGCGCTGGGGACGCGGGTGCCGTACGGGCCGGACAAGGAGGTGATCGTCCAGGACGCGCGCGACACGCACGTGCTGCTGCTGCTCAGCGGCATGGTGAAGGTGCAGGCCGTGGACGAGGACGGTGAGCACGCGCTGCTGGACATCAGGATCGCGGGTGACGTCGTCGGCGAGATGGCGGCGTTGAGCGGGAAGCCCCGGTCGGCCACGGTGCGCACCTGCGGGGAGGTCGTGGCCCGCGCGATCACCCGCGCCGACTTCCAGGCGCTGCTGCTGCGCCGCCCCGAGGTGGCGATGGAGCTGGTGCTGGTGGTGGGCGAGCGGTTGCGCTGGTCGATCGACCGCCGCCGCGACTTCCTGTCCTGCCCGGCGCCGGTGCGGGTGGCCCGCGTGCTCGTGGAGCTGGTGCAGACCTACGGCAGGCAGGACAAGGACGCGTGGCGGCTGGGCATCCCGCTGACCAAGGTCGAGCTGGCCTCGATCGCGGGCATGAAGCCGCGCACGGCGGAGAAGGCGTTCAGCGACCTGCGGCACGCGGGCGTGGTCGTCAGCAACCTGCGCCGCGACGTCCTGGTGCCCGACCTGCGGGCGCTGCGCCGCTACGCCGGATCCTGAGAAACCGCGCGTTCGGGTGGAATCCCGCGCTTCGGCGAAACGAACCGGCCGTGCGGCGCGACCTGCACGCCGGGGGATGACAACGGTTGCAGCGAGTTGCGGATACGACGCATTAGGGGTGGATGGTGCTGATGTCATGGTCACCGAGCACGACCCAGCCGGAGCAACCGGTGTGGCCGCACGACAGCCTGCTGTCGCGGCTGCGCGATCAGGCGCGCGACGAGCTGCTGGCGATGGGCACGGTGGTGCGGTACGCGCCGAACCGGGACGTGATCGTGCAGGACGCCCGCGACACGCACGCGCTGCTGCTGCTCGACGGCGTGGTGAAGGTTCAGACCACGGACGAGACCGGCGACACGGCGCTGCTGGCGATCAAGGCGGCCGGTGACTTCGTCGGCGAGATGGCGGCGCTGGACCGCAAGCCGAGGTCGGCGAGCGTGATCACGTGCGGCGAGGTGACCGCGCGGATGATCAGCAGCAGCGAGCTGATGGGCTTCCTGCACCGCCGCAACGAGGTCTTCGTCGAGATGATCGGCATGGTCAACGAGCGGCTGCGGTGGGCGATCGAGCGCAGGCGGGACTTCCTGGCGCGGGCGGCCGACGAGCGGTTGGCGAAGGTGCTCGCGGAGCTGGTGCGCACGCACGGCCGCGAGGAGCCGGGCGGGTGGACGCTCGGGTTCCCGCTGACCAAGGTGGAGCTGGCGTCGATCGCGGGCATGAAACCGCGCACGGCGGAGAAGGCGTTCAGCGACCTGCGCAAGGCCGGGGTCGTGGTGAGCCACCTGCGCCGGGACGTGCTGGTGCCCGACCTGGACGCGCTGCGCGCCTACGCCCAGCGCCCGCCGCGCTGAGCGGCGGGCCGGGTTGGGTGGCGGGCCGGGCTGGGTGGCAGGCCGGGCAGGGCCGGGTGGCGGGCCGGGCAGGGTTGGGTGGCGGGCCGGGCAGGGTTGGGTGGCTGGGCAGGGCAGGGCGGGCAGGACTGGGCTGAGCGCCAGGTCAGGCCGGGCTGAGCATCGGGCCGGGCAGGTATCGAGCTAAGCGGGCATCGGGCCGGGCTGGCATCGGGCCGGGCCAGCCGTTGGAGTGGGCTGGGCACTGGAGTGGTCGGAAAAGCGGTTGCCCCGCCGGGTGCGGGCGGGGCATGGTGGGTGAGCACAGCGACTCGCGGGCCGGAGAGCCCGGAGCGGATTCGGGGAGGAGGTGTCGACATGGCCATGACACCTGTCCTGGACGCGGCACCGGCCCGTCCACCCACCCCGGCGCTCCACAGGGTCTGACGCGGTCGCGCGGCCCGACGTCGGGGTGATCACCCACTTCCCGCTGGGAGCCCCGCTGTGCGCGAGCACGCGATCACTACTGACGCACTGCACGAACTCAAGATCAACTTCAATCACGGCGGTCGATCTGACGACGCCGCCGATGTCGACGCGCCCGAGTCCGGTTCGGGCGGTGGCGCGGGTCGCCACGACGACACCGATACCCGCTACGGCGACGCGGACGAGGCCGGCACCGGCTACGACGACATCGATGATGTCGACGCCGGTTACGGCGACACCGATGATGTCGACGCCGGCTACGGCGACACCGGCGACGTCAACGCCGGCTACGGCGACACCGACTACGACGCCGGTCATGACGGTGGCGACGGCGACGACGCCAGCGACGACGACGCCGACCCGCACAGCCGCTGGTCCGACTACGAGCTGGACGACTACGGCCCGCGCGAGGTCAGGACCCGTGTCCGGGTCGTGCGGGACGACGAGGAGAACGTCCGGCGCGGCAGGCTCACCGAGGAGGCCAAGAAGCGGCTCGGCGAGTCCCGGCAGCTCACCGGGCCCGAGGACGGCGACCGGTGGTCCACCTGGGGCAGCGCCGACCAGGGGCCCGCGCCGCACCCGGCGTGGCTGGTCACCGACCTCGGGGCCGTCGACCGGGAGCTCGGGCTGATCAAGTCCGGCAAGGAGGCGGACGTCTCCCTGCTGGAGCGCGCCACGCCCGACCGGTCCTGCCTGCTGGCCGCGAAGCGGTACCGGGACAACGACCACCGGCTGTTCCACCGGGACGCGGGCTACCTGGAGGGCCGTCGGGAGCGGCGGAGCCGGGAGGCCCGCGCGATGTCCCGGCGCAGCGCGTTCGGGCGGAACCTGATCGCCGAGCGGTGGGCGGTGGCCGAGTTCGCGGCGCTCGGCGCGCTGTGGCAGCGCGGCGTGCCGGTGCCCTACCCGGTGCAGCGCGACGGCACCGAGGTGCTGATGGAGTTCATCGGCGACGGCGCCCAGGCCGCGCCCCGGCTCGCCCAGACCAGGCCCGAGCCGGACGCGCTGGTGGACCTGTGGCGGCAGCTCGGGTCGGCGCTCACGGGGATGGCCGCCGCCGGGTACGCGCACGGCGACCTGTCGCCGTTCAACCTGGTGGTGCACGACGACCGGCTCGTGGTGATCGACCTGCCGCAGCTGGTCGACCTGGTCGCCAACCCGCGCGGGGCCGAGTTCCTGGCGCGCGACGTGCGGGTGGTGGCCGAGTGGTTCACCGCGCGCGGCCTGCCCGCCGAGCTGGCCGACCCGGTCGAGCTGACCGCCGACCTGCTCCGGGAGGCCGGGCTGGCGTGAGACGGGCGCCGCCGGGTGGGAGGGCGCGCCCCCTCACCCGGCGGCGAGCGCGGCGCACGTGCGGTGAGAACGCGGGACACCACCCGCGAACACGTGCGGTGGGAGCGCGATCTCGTTGTGTCACCGATGCTTTCGCGCGGTCGACGCCGCTCGGTCACCACCCCGCCACCCCACGTCGCGACGGTGCGCGACGACGGCGCCCGCCGGGCGTCACCGCGCGTTCGCGGCGCCGCGAACACCGGCTGCCGTCCGTGACCGCCGCGCGAACGCGCCCCGTGACCACAGCTCGGGTCCCGGTCGCGCACGGGCCGCCCGACCAGGGCCCCTTCCACCACCGGGTCGTCCCGGAACCGGAACCTCTTGCGCCCCAGCGGTTTCCGCGTTCGGAGAGCGGACGCCCGCGCGCGGTCGCACCACCGTCAGGTGGAACCCGGCCACGTCCGGGTGCCGCGCGCGCCGCGCCCTCAGGCGGCACGGGGGACCGCCGAACCCCTCGGTGACCGCCCGCAGCCCGCCGAGCCAGCCGCCCCCCGACCTTCCCGACGTCCGCGCAGGTCAGAGCCCCGCCGCCGAAACTAGGCCGAGTGGCCGCGACCCAATGGATGATGATCAGCTAGACTGGTCAACGCACCGCACGAGGGCGCTACATTCCAGCGCCCCGAGGTCACCACTCAGGACCACCCGGTGCTCCACCCAACCGTCGGCGCTACGAAGCGCCGGGCCCGTCCGCGCGATCGCGCCTGCCCACGAGTGCAGAGCAATCCCCGTGACGTGCCGTGTCCCGGAGGTATGTTTTGCCACCCGTGTCCCAGAGCCGTTCCGAGCGCCCGCAGTCCTCTCGCAGGCCCCGCAGGCGCTCCGGCCAGGGCAACCGCCGTCCGCAGCACGTGGACGCGCCCCTCGCTTCCACCGTTCCCGACCACGTCGAGAGCACCCTCCCCGAGGGCCCGCTGCCCTCGTTCAGCGAGCTGGGCCTGGCCGACGAGCTGGTCCGCGCGCTCGCCACGGCCGGGATCACCGAGCCGTTCCCCATCCAGGCCGCGACCCTGCCCGACTCGCTCGCGGGTCGCGACCTGCTCGGCCGGGGCCAGACCGGCTCCGGCAAGACCCTCGCGTTCGGCCTGGCGCTGCTGTCCAGGCTGGCCGGTGGCCGCGCCAAGCCGCACATGCCGCGCGCGCTGGTGCTGGTCCCCACCCGTGAGCTGGCCATGCAGGTCGAGGAGGCGCTGTCGCCCTTCGCCCGCGCCCTCGGCCTGTGGTGCCGCACCGTCGTGGGCGGCACGTCCTTCCCGCGCCAGATCGACGCGCTGCGCAGGGGCGTCGACCTGCTGATCGCCACGCCCGGCCGGCTCTCCGACCACGTGCGCCAGGGCACCGCGGACCTGTCCGAGGTCATGTTCACCGCCCTGGACGAGGCCGACCAGATGGCCGACATGGGCTTCATGCCGCAGGTGCGGGCCATCCTGGACCTGACCCCCGAGAACGGGCAGCGGCTGCTGTTCTCCGCGACGCTCGACGGCGACGTGGACAAGCTGGTCCGCCAGTACCTGCACGACCCGGTCGTGCACTCGGTCGCGCCGCCCACCGGCAGCGTCACCACCATGGAGCACCACCTGCTGTTCGTGTCCGCCGAGGACAAGCAGTCGGTCGTGACCGAGGTGGCCGCCCGCGAGGGCCGCACGATCATGTTCGTGCGCACCAAGCACCACGTGGACCGCCTGGCCAAGAAGCTGCGGTCGATGGGCGTGCACGCGGGCGCCCTGCACGGCGGCAAGGCGCAGAGCGCGCGCACCCGCGTGCTCGGCCAGTTCCGCGAGGGCACGACCCCGGTCCTGATCGCCACGGACGTCGCCGCGCGCGGCATCCACGTGGACGACGTCAGCCTGGTCGTGCACGTGGACCCGCCCGCCGACCCGAAGGACTACCTGCACCGCGCGGGCCGCACGGCGCGCGCCGGGCAGTCGGGCACGGTCGTCACGCTGGTCACGCACGACCAGCGGCGCGCCGTCCAGGGCCTGACCTCGCGCGCGGGCATCCGCCCGGAGTCGACCAAGGTCCGTCCCGGCGACGACGAGCTGATCCGCATCACCGGCGCCCGCGAGCCCAGCGGCGTTCCCGTGGTGGAGCCCGAGGTGCAGCCGCGCGGTCGTCGCGGCGGCGCGGGCGGTGGCGCGGGCGCGCGTCGTGGCGGCGGCGGGTTCTTCCGCGGCGGTCGCGAGGGTGGCCGCGGCGAGGGTGGCGGCCGTGACCGCGACCGCTCGGGCGGCCGTCCCCGGCGCAGCGCGGCCCCGCAGCACTGACGAGTGACGAGTGACGCGCGGCGCCGGTAGCGGGCGCTGACGCGGAACGGCGAGAGCCCCGGTCCCCTGGTGGGACCGGGGCTCTCGTGTTGCCGGGGGACGGGTGGGGTGGCGGGAGCACCGGTGTCGCTGCGTGATGTGGCCGCCGGGCGCCAGCCGGGGCCCGGTTCCCGAGCGTGACGCCCGCGCCCGGAGTCCGGTGGCCGAGCGTGATCCGGACCGGTGGCCGAGCGTGAGGTGACGGCCGGGGTGCGCGGTGGCGGTGCGTGACGTCGCGCGGGAGGCCGGGGCGTCCCGCGCGACCGGCTCACGCCTGCTCGGGCAGTTCCCCCGCCAGGCCGGCGACCGGGCCGACGACGATGATCGCGGGCGGGCGGACGTGGTGCGCCGCAACGGCTTCCGCCAGACCGTCCAGAGTGGACCGCACGATCCGCTGGGCGTCCGTGCTGCCGTTCTCGACGACGGTCACCGGCGTGTCCCCCGGGCGGCCCTCGCGGAGGGCTGCGGCGAACGCGGCGGCGCGCTCCACGCCCATCAGGATCACCACGGTGCCGCGCAGCCTCGCCAGGGCGCCCCAGTCGACCAGGGAGCGCTCGTCGTCCGGCGCGACGTGGCCGGACACCACCACGACCTCGTGCGCCACACCCCGGTGCGTCACCGGGACGCCCGCGAGGGCGGGCACGCCGAACGCGCTGGTCACGCCCGGCACGACGGTGACCGGCACGCCCGCCTCGGCGCAGGCGATCAGCTCCTCGAAGCCGCGCCCGAACACGTACGGGTCGCCGCCCTTGAGCCGGACCACGAACTTCCCGGCCTTGGCGTTGTCCACGAGCGTCCGGTTGATGAACTCCTGCGCGGCGGCCCGCCCGTACGGGATCTTCGCGGCGTCGACCACCTCCACGTGCGGCGGCAGCTCGTCCAGCAGCCACACCGGGCCCAGGCGGTCCGCGACGACCACGTCGGCCCTGGCCAGCAGGCGCCTGCCGCGCACGGTGATCAGGTCGGGGTCGCCGGGGCCGCCGCCGACCAGGGCCACGCCCGCGGGCTGGTCGTGCTGGTCGGCGAGGGTGCCGTCGCGCAGCGCGGACAGCACGCCGTCGCGCACGCGCGCGGAGCGGTTGTGGTCGCCGCTGGCCAGGACGCCGACGAGGAGGCCGTCGTGGTTGCCGGAGGCGGGCGTGACGGCGGTGCCGAGCGCGCCGACGTCGGCGCGCACGCAGAACACGCGGCGGGCCTCGGCGTCGGCGGTGATCCGGGCGTTCACCTCGGGGTCGGAGGTGCAGGCGAGCACGTACCACGCGCCGTCCAGGTCGCCGTCGGCGTAGCGCCGGGCGTGCCAGGTGACCGCCCCGGAGTCGACCACGCCCTGGACGGTGGGGGTGACCTCGGGCGAGACGAGTTCGACGCGGGCGCCGGACGAGACCAGGCGCGGCAGGCGGCGCTGGGCGACGGACCCGCCGCCCACCACGACCACGCGCTTGCCCGCCAGGTCCAGGCCCACCAGGTAGTGCTGTTCTCCGTGCATGGCGAGAAGCATCCCCGGCGGACGGGCCCGCGCCCAAGGTGGGTGTCCCACATCACGGGAAGCGGGTGTCGGAGTGTGAGCGGACGGCGGGAGGGCGCGCGGCGGCAGGGCGCAACGGCCGCGCCGCGCGGGCGGAAGGGCACCGGGCCGGGCGGGGCGAACGGACCGGGACCCGCGGGCGGGCGCGGGCACGGGGGAACGCGCGGACCGACCGAGGGCTGACCGGTCCGCGCGCCCGCCCGCGCCCGGTCGACCGGAGGACGTCGGTCACCGGGCGTGGGGCGCGCCCGAGGGCGCGCCCCCGGCGGTCATCCGATCTGCGCGCTCAGCACGCTGTAGTAGGCCGCGACCCTGGCGTACACGCCGGGGTAGTTCGGCAGTGCGCAGCCGTTGCCCCACGAGGTGGCGCCGATCAGCTTGCCGCCCGCCACGAGCGGGCCGCCCGAGTCGCCCTGGCAGGTGTCCTTGCCACCGGCCGGGACGCCCGCGCACACCATCGAGGTGTTGCTGTACTGCGAGTACGCGGTCTTGCAGGTCGCGTCCGAGGTGACCGGGACGGTGACCTTCAGCAGGTAGCGGGACGTGGAGCAGCCGGAGCAGGTGGCGCCCCAGCCGTACGCGACGGCGTTGGTGCCCGCCGCGTACAGGGCCGTGTCGGACGGGGTGGCCAGCGGCAGGTAGGTGCCGCTGACGCTGGTGCCCAGGGTCAGCACGGCCACGTCGTAGCCGCTGGTCGCGGTGCGGTAGCTGGGGTGCGACCAGATGCTGGAGACGGTGGCCACCGTGCCCGCGGTGCTCTGCTTGTCCTCGCGGCCGATCACCACGCGGGTGCTGGACGCCGAGCGGCCGGCGACGCAGTGCGCGGCGGTGACGACCTTGTTGGCCTTCACCAGGGTGCCGCCGCAGAACTGGGAGCCGGAGGAGGAGGCCAGGTACACCGCCCAGGGGGCCTCGCTGATCGAGGCCCTGGCGCCGCCCACGATGAACGGGGTGACGTCGGACGCCGAGGACACCGGGGTGGTCATCAGGCCGATCGCGGCGGCAGCCACGCCCAGGCCGATGAACTTCGCCAGGCGACGCAGGGTTTTCGCCATCGGAGTTCCTTTCCGTGCAGGAGTGAGCACTCACTGCAACGCACCCGACGGCCTCCCGGCAACCTCCTTCAGCGGGACTGAGGGGGCTTCACAATTGACCAGTGACTCCGGTCACACGAACGACATCGGCGTGTACCGGCCCGGCAACAACCGGTCCCGCGTCCGGCGCCACCAGCGCCACCGCGACGCCCTGCTCGGCCAGCCGGACCGCGCCGTCCGCGCGCACCGACGTGCCCGGCCGCAGCAGGTGCCTGACCTGGTCGACGCACTCCGGCGGCCCGACCACCACGGACGCGCGGCGCAGCTCGGCCTCGGCGCGCGGGGTGCGGTCGTCCGCGCCGCCCGGCCCGAGGCCGATGAGCGCCAGCCTGCCCCTGGGCAGGACGCGGGCGGCGGCGACGGTGGCCCGCGCGCCCTTGACCTTCTCGGCGGCGATCTCCACCCGGCCGCCCGCGGACAGCTCGGCCGCGCCGCGCAGCGCGGCGGCCTCGGCGACGCTGGGGATGCCGATGGCCAGCTCCACCGGGTTGGGCACCGGGATGACGGCCAGCTCCTCGCCGGGGTAGCCGAGCAGGGGCGTGGTGGTGGAGCCGTGCCAGAAGCCCCAGTCCTCGACCGCGTCGACGATGCCGGGCTCCTCGGTCTTGCGGTCGAGCGTGGCGAACGCGCGCACCGCCCGCAGGTCCAGCCTGCCGTCGGCGGCGAGCTTGGCGAGCGCGCCGGAGACGTCGGTGGACGTGACGCCGGCGCTCGCGCCGATGCCGATCACGAGCGTCCTGGGGATCACCCGGACCACGTGGTCGCCCAGCTCGGTCCTGGGCACCCGGTCGTCCAGCAGCACCGTCCACGCGGCCTCGTGACCGGCGGGCAGGACGTTGTCCGGCAGCGCGGGCAGCGGGAAGCCGAGCGGGTTGGCGAGCGCGACCGGCTCGCCCGCGCGCATCGCCTCGCCGCACGCCGCGGCGTCGCCCTCGGCGGTGGCGTCGAGCAGTTCGAGCAGCTCGTCCAGGGGGGACGCGGTGGGCGGGGCGGTGGTGACGGCGGTGCGGCCGAGCACGTCGGCGACCCGCTGGGCGAGCGCGTCCGCGCCGCCGAGGAGGGCGATGGCGAACGCGCCGTCGACGCACACCACACCGGGGTCGGAGCGCTCGTCGCGCAGCAGGGGGGCCACGAGGCGGACGACGGTCTCGCTGCCCTCGAAGAACACGGCGCTGCCCAGCACCGGCCACATCCGGCGCAGCGCGGGCGCGACGGGGCCGTCGGGGACGACGGCGTCCGGGCCGAGGAAGGCCGCGAGCTCCTTGGCCTGCGCCCTGCCGCGCTCGGTCGACGCGAACAAGCCGATCACGCTGCCTCCTTGCCGGGGTGGGGGTGCCATCCTTCCCCGCCCGGCGCGGTGGGGTGGGGGCGGGTGGGGTGGGGGGCGGCGGGGAGAGGCTGAGGGGGGACGAGAAGGGCCGGGAGGAGCGGGCGGGGCTGCGCGAGGCGGGCGGCGCAGGCGGAGCCGGACGGAGCCGCGCAGGGCTGCGCGAGGCGGGCGGCGCAGGCGGGACAGGACCAGGCGGGGCTTGGTCTCGCCAGGCGGGACCAGGCGGGACCAGGCGGGACCAGGCGGGGTCGGGCGGGGTCGGGCGGGGTCGGGTTCGGGCTTGGCGGGTTCCGGGTGCCGGGTGGGGGTCTCAGGCCGGGCGTTCGGCCCACAGCACGGTGACCGGGTCCACCGCGCGCAGGTGGTCGTCCTCCAGCCTCGCGGCGGACAGCTGGGTGCCGGACACCGCGTAGCCGCCGTCGCGGAGGGCGTCGTGGGACGGCAGGACGGCGTCGAGGCGGGTGGTGGCCACGACCACGCGGCGGGCGCCCAGGGCGGCGCAGGTGCGCACCGCGCCCGGTCCCCCGCCGCCGACGAACACCGCGTCGGGGCGCGGCAGGTCGTGCGGGGCGAGTTCCACGTCGGACTCGACCACGCGCACGTCCACGTGGTGCGCCGAGGCGTTCGCGATGATCCGGACGCACTGCACCGGGTCGCGCTCCACGGCGACCACGGCCGCGCCCAGGCGCGCGCACTCCACGGCGACCGCGCCGGGACCCGCCGCCACGTCCCACACCAGGGCCCCGGACCTGGGGCCCAGCTTGGCGAGGACGAGCGCGCGGACCTCGGCGGTGGCGACCAGGCCGTCGCCCCGGTGCGAGAACTCGTCGTCCGGCAGCGCCCACCGCGAGGTGTCCGGGAGCAGCGGCTGCTCGGCGAGGCACAGCACCGGGAGCGGCTCCGGCCAGGAGCGGAGCGCGACCTCGGCCGGGTCCACTGTGGACGGTCCGGGCGCACCGGGCACCACCAGGGTGCGCCGCCAGCCCGCGAGGCCCCTCGCCAGCGCGGCCGGGTCCGCGTTCGCGACCAGCACCGAGGAGCGGGCCAGGCACACGTTGCGGGCGTGCGCGAGGCCGTGCTCGGCGGCGTCCACCACCGTGACGGCGGACCAGGTGCGGCCGGTGTCGGTCAGGAAGCGGTGCAGCGCCGGGACGTCCACGCCCTCAGCCTGTGCGCTTGGACTTCTTCCCGCGCGCCGGGGCGGGCTTGCGCGGGGTGGTGCTGGCCTGGACGGAGACGGTCCTCTTGCGCGCCGCCGCGACCGGGGGCTTCCTCCTCGGCTCCGGCGCCTCCTCGGGGGAACCGGCCTGACCGGGCAGCGAGTCCACGGCGGGCTCCTCGGCGACCGGCCCGGCCGCTGTGGGCTCAACCGACCCCGCGGGCTCGGCGGGCTCGGCCAGCGACCGCGCTATGGGCAGCTCCGCGCCGTCCGCGCCGGACTCCTCGCGCGCCCTGGCCCAGCGGGAGCGCGCGGTCTCCTGCAGGTCGTGCACGGCCGACCAGGCGGCCTCCGAGCGGGACTCGGCGCCCGTCGCCCGCGCCGTCCGCCACTTCGAGGCGCGGGGCTGGCGCACCGGCTCGTCCCCGATCGGCGCGCCCCTGCGGACCGGCGCCCTGAGCGCGTCCCCGACCAGGAACAGCGTGCTGCGGTAGAGCTTGTGCTCCTTGACCGCCGACTCCAGCTCGCCCAGCGTGGTGCGCACGAGCACCGCGTCCGGCAGCGACACCTTGTAGGCGATCACGACCGGCGTCGTGTCGGCGTACCCGCCCGCGCGCAGCTGCTCGGCGACGCGGTCGGCGCGCGCGGCCGACGCGGACAGGGCGAGCGTGGTGCCGTGGGCGGCCAGCTCGCGCACGTGCTCGGCGCTCTCCGGGCTGGCCAGCACGAGCGACTGCGCGACCTCGGAGGTGGTCAGCTCCCGCCCGACCGACGCGGCGGCGGCGGACACCTGGGTCACGCCCGGCACGACCTCGATCTCCAGCCCCAGCCGCAGGCACGCGTCGTGCTGCTCGCGCAGCCCGCCCCACGTGGCGGGGTCGCCCGCGTGCAGCCGGACCACGGCCTGGCCGCTCGCGGCGGCCCTGCGGTAGACCTCGACGACCTCGGACTCGGTGACGCGGGAGAAGTCGACCAGCTCCGCGCCGGGGCGGGCGTGCTCGCGCACGCACTCGGCCTCGACCACGCTCGGGGCCCACACGACGACGTCGGCCTCGGCCAGTCGCCTGGCCCCTCGGAGGGTGATCAGATCGGCGGCACCGGGGCCGGCACCCACGAAGGCGACCCGACCTGTCATCTGAGAACTCCCCACGACGTGCTCGGTGTGAACGGCCCGACCGTATCGCGCAGGGCCCTCTCCCCATCGAGCGCCCTGATCCCGGCACGGAGCGCGACGATCGGGGTGGACGCGCCGTGAGCGGCACCCCGGATGCCGCGCCCCTGGGCCGTCCGGGTGAGCGGCGGGGGTCAGGCCGGTGGGTGCCCCCAGGCCGCGCAGGCGGCGGTGAAGCGGTGCGCCGCCCCTGGGATCGAGGCCGGGTGGGTGTGCAGGTAGGACGCGTGGACGTTGCCGAGCACGAAGCCCTCGGCGGCCGGGCGGCCGTCGTGCCCGCGCCAGCGCCACGCCGGGTCGGCGCCGTGCGGGGTGCTCAGCGCGGTGCGGTGGAACTCGTGGCCGGTGACGCGCGCGCCGACCGGCAGCAGCACCGAGTCGACCGGGGCGACCGCGTCCCGGTAGCCCAGCACCAGGCGCGGGGTCATGGCGGCCTCGGAGTCGACCACCCCGCACATCGGGGCGCCGTCGAGGGACTTGGCCAGGTACAGCAGGCCGCCGCACTCGGCGTGCACGGGCGCGCCCGCGCGGGCCAGCGCGGTGATGGCGGCGCGCAGCGGCTCGTTGGCGGACAGCTCGGCCACGTGCTGCTCGGGGAACCCGCCGGGCAGCAGCAGCCCCGAGGTGCTCGCGGGCAGGGTCTCGTCGCGCAGCGGGTCGAAGACGACGACCTCGGCGCCCGCCGCGCGCAGCAGCTCGGGGTGCTCGGCGTAGCCGAAGGTGAACGCCGGGCCGCCGGCGACCGCGATCACCGGTCGTCGCGCGCCGGGAACCGTTGCGGCGCCTGGGTTTTCGATCGCAGCCGCGATCTCGGCTTCCGGGTCCCAGGCCCGCGCGGCGACCGGGTTGGCGGTGGCCGCCAGCGCGCGGACCGCCGCGAGGTCCACGTGCGCGCCGACCGCGTCGGCCACCGCCTCCACCGCCGCGACCGCCTCGTGGCCGTGCTCGGCGGCGGTGACCAGGCCGAGGTGGCGCGAGGGCAGCGCGAACCGGTCGTCCCTGGGCAGCACGCCCAGCACGTCCAGGCCCACGTCCGCGCAGGCGCTCCGCAGCACCTGCTCGTGCCGGGGCGACCCGACCTGGTTGAGGACCACGCCGCCCAGGCGCACTCCGGGGTCGTAGCCCCGGAAGCCGTGCAGCAGCGCGGCGAGGCTGCGGCTCTGGCCGCGCGCGTCCACGACGAACAGCACGGGCGCGCCGAGCAGCTTGGCCACGTGCGCGGTGGAACCGACGCCGTCGGTGTCGATCCGCCCGTCGAACAGGCCCATGACGCCCTCGACCACGGCCAGGTCCGCGCCGCGCGCGCCGTGCGCGAACAGCTCGGGCACCCGGTGCTCGCCGACCATGACCGGGTCCAGGTTGCGACCGGGGCGGCCGGTGGCGAGCGCGTGGTAGCCGGGGTCGATGTAGTCGGGGCCGACCTTGAACGGGGCCACCGCGTCGCCCGCGCGGCGCAGCGCCGCCATGAGCCCGGTGGCGACGGTGGTCTTGCCGCTGCCCGAGGCCGGGGCGGCGACGACCAGCGCGCTCACCACTCGATCCCCCGCTGGCCCTTCTGGCCCGCGTCCATCGGGTGCTTGACCTTGGTCATCTCCACGACCAGGTCGGCGGCGTCCACGAGCGCCCGCGGGGCGTCCCGGCCGGTGATCACCACGTGCTGGTGGCCGGGGCGGTTGACCAGCACCTCCACCACCTCGTCGACGTCGATCCAGCCCCACTTGAGCGGGTAGGTGAACTCGTCCAGCACGTACAGGCCGTGCCGCTCGTCGGCGATGCGGCGGGCGATCTCGCGCCAGCCCTCCAGCGCGGCGGCGGCGTGGTCCTCCTCGGTGCCCGCCTTGCGGGACCAGGACCAGCCCTCGCCCATCTTGTGCCACTGCACGGGCCCGCCCTGGCCGGTGCTCTCGTGCAGCTCGCCGAGCGCGCGGAACGCGGCCTCCTCGCCGACCTTCCACTTGGCGGACTTCACGAACTGGAACACGCCGATGTCCCAGCCCTGGTTCCAGCCGCGCAGGGCGAGGCCGAAGGCGGCGGTGGACTTGCCCTTCATCGGGCCGGTGTGGACGAGGAGGAGGGGGCGGTTGCGGCGCTGGCGGGTGGTGAGGCCGTCCGACGGCACGGCGGTGGGTTGGCCCTGCGGCATGTCGTGGCTCCAGGTGTGGTGGGGAGGGGGACGCCCGCGGCGCGCGGACCGGCGCGACGGCGGCGGGCGGGGTCGGGCGGGGGGAGCGGGTCGGTCAGGCCGCGCGGGCGGCGCGGACGACGCCCGCGACCTGGTCGGCGGACAGCTCCTCCAGGCGCAGGCACGCGCCGTCGAGCGCGGCGGCCACGCGGGCGGCCATGCCGAGGCGGACGTGGCCGCTCTCGCAGTCCACGACCACCGACGCGACGCGGTCGGCGGCCAGCAGCCCGGCCGCGCGCAGGGCGTCGCGGACCGGGTCGCCGCCCGCGCCGGTGGCGGTGGCGCGGCCGTCGGTCAGCAGGACCAGCAGCGGGCGGCGGCGCGGGTCGCGGACCTTCTCGGACTGGAGCAGGCGGCGGGCGCGCAGCAGGCCGTCCGCCAGCGGGGTGCGGCCACCGGTGCGCAGGGCGCGCAGCCGGGCGGCGGCTGCGTCCACGGACGTGGTCGGCGGCAGCGCGGTCTCCGCCTCGGAGCCCCGGAAGGTGATGACGCCGACCTTGTCGCGGCGCTGGTAGGCGTCGCGCAGCAGGGAGATCACCGCGCCGGACACGGCGGACATGCGCTGGCGGGCGGCCATCGAGCCGGAGGCGTCCACGACGAACAGCACCAGGTTGCCCTCGGTGCCCTCGCGGACGGCCTTGCGCAGGTCCTCGCCGCGCAGCAGCAGGCCGGGACCGGTGCGGCCCCTGGCGCCCTGGTGCGGGGCGGCGGCGGTGAGCGTGGCGACCAGGTGCAGGCCGGAGCCCTCGGTGGTGGAGGGGCGCACGGCCCGGCCGCTGCGGGAGCGGGCGCGGGAGCGCTTGCCGGACGCGCCCTCGCCGACGCCGGGGACCTGGAGCAGGCGGGTGCGGAACGCCGGGGACGGGCTGTGCGTCCTGGTACCGCCGGAGCCGCCCTGCTTGCCGTCCTGCTGGGACGGTCCGGGCTGCTCGCCGCCCGGCTCCTGCGGGCCCTGCGGCTGGTCGGGGCCCTGGCCGTCGTCGGGACCGCCGCCGTCCGGGCCGCCGTCCGGGCCGCCGTCGTCGGGACCGTCCGGGTCGTCGTCGGGCTCGTCCTGCGCGTGCTCGGCGCCCTGCCGCATGGCGTCGGAGAGCTGCTCCTCCTCCATGCCGGGCTCGTCGAACGGGTCGCGGCGCTTGCGGTGCGGCAGGGCGAGGCGCACGGCGGCCTCCACGTCCTGCTCCTGCACCGCCTCGGCCCCGCGCCAGGCGGCGTGCGCGGTGGCGGCGCGGGCCACGACCAGGTCGGCGCGCATCCCGTCCACCTCGAACGCCGCGCAGATCCCGGCGATGCGGCGCAGCTCGGCGTCCGGCAGCGCCACGGACGGCAGCGCGGCGCGGGCCTGCGCGATGCGGGCCGCGAGCGCGGCGTCCTCGGCCTCCCAGGCCTTCGCGAACCCGGCGGGGTCGGCCTCGTAGGCCAGGCGGCGGCGGATCACCTCGGCGCGGGTGGGCACGTCGCGGGCCGCCTTGACCGCCACGGTCAGGCCGAACCGGTCGAGCAGCTGCGGGCGCAGCTCGCCCTCCTCCGGGTTCATCGTGCCCACCAGCAGGAACGACGCCGGGTGCGACACCGAG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GGGCGCGCGCCCGGCGACGGAGCCGCCGACGACGGCGAGCGCGGCGGGCGCGGCGACGAGCTGGGAGGCGAGCTGGACCGCGACCAGGGCGAGGGCGGCGACTAAGCGGGAGCTGATGCGCATGGAGCACCTCTTTACGACGGGTAGCCGAGTGGCGACTCACCGTAGCCGCACCACAAAGATCACATCAAGTCAGGATATTTTCCTGTTAAGATGCCGTAGTTCCGAAAAATCCACGGTCTGTGTCCTGCGTCACCGCTGTCTGTCCGGACCATAGGGGGGTACTTCCGTTGCAGTTCGACCTGACCACGCTGCCCGCGTTCCTGATCGCCTGCGCGGTCGTGGTGCTCACCCCCGGCGTGGACTCCTTCCTCCTGCTGCGCACCTCGATGCGCTCGGGCACCCGCGCCGGCCTGCTGGCCCTGGCGGGCATCCACACCGCCGCAGCCATCCAGGTCGCGGTCGTGATCTCGGGCCTCGGCGTGGTGATCGCCGGCTTCCCGCCCGCGCTGACCGCGCTGCGCTGGATCGGCGCGGCCTACCTGCTGTACCTGGCGCTGTCGATCACCCGCGACCTGGTGCGCAACCGGGGCCGGGCGCCCGAGGAGGGCGAGGTCGTCGCGGACCGGCCGTTCCGGCGCGGCTTCCTGACCAACATCACCAACCCGAAGATGCTGCTGTTCTCCCTGGCGTTCCTGCCGCAGTTCATCGGCTCCGGCGACCCCACCCCGCAGCTCGCGATGCTCGCGGCGGTGTTCCTGGCGCTGGCCGCCGCGTGGGAGGGCACGATCGTGCTGGCCGCGTCGGCGGTCGGCGGGCGGCTGCGCAAGCCGGGCGTGACCACCGCGCTGGACGTGGTGTGCGCGGCGGTCTTCGCCACCATGTCGGTCGGCCTGGTCCTCTGACCGGGCCGCGCCGCGACCGTCAGGTGTAGGCGCCCACGCGGGTGTACACGCCGGGGTACTCGGGCCGGGCGCAGCCGACGCCCCAGGACACCAGCCCGGCGAGCCTGCCCGCGATGACGAACGGCCCGCCCGAGTCGCCCTGGCAGGCGTCCTTGCCGCCGTTCGGCAGCCCGGCGCAGAACATCGACGACGACTGGTAGTGGCCAGGGTAGGCGGCGGAGCACACCTCGTTGGTCTGGAGCGGCACGGACACCTTCCGCAGCACCGGCGAGGTGGTCCCGCTCTCCGAGGTGCGGCCCCAGCCGAACGCGGTGCCGGTGATGCCCGCCCGGTACAGCCCCGTCTCGGACGGCTTGGCGAGCGCGATCGCCTCGTACGGCATCGGCGTGGACGTCAGCAGGTAGGCGATGTCCGCGCCGGTGGTCGCCGAGCGGTAGGCGGGGTGGACGTACACACCGGACACCGGGTGGATCGTGCCACCGGGCTTGGTCACGTCCAGCCTGCCCGCCACCACCAGCACGTCGCCGCCGATCAGCCCGCTGACGCAGTGCGCGGCGGTCATCACCTGGTACCGGCTGATGATCGCGCCGCCGCAGAACTGCCTGCCGTCGGGGTCGACCAGCGCCACCACCCACGGGTAGGGGTTCGGGGCGTCCACGACCACGCCGCCGACGATCCTCGGGTCGGCCCCGGCGGGCGGCGCCACCGCCACGCCGGTGAGCAGCAGTGCCAGCGCCATCGCCACGCGCATCAGAGTCCGCATACCGGCCAACCAAACCCGGCCGCCGCGACCGCACAACTCGGGCACACGGTCGGGTGATCGGGTGTGGTCGGCCGGCGCGGCGCTCAGCCCTTGAGCTGCTGGTCGATCAGCGCCCGGTAGGCGGTGATCCGCGAGTACACGCCGGGCTGGCCGGGCCGCGCGCAGCCCTCGCCCCACGAGGTGACGCCGACCAGCGCGCCGTTCGCGACCAGCGGGCCGCCGGAGTCGCCCTGGCAGGTGTCGATGCCCCCGCGCGGGTAGCCCGCGCAGACCATGGCCGCCGGGTCGAACCGGCTGTAGTCGGCGGCGCACTCCTGGTCGGACATGACCGGCACGTTCGCGCCCAGCAGCACCTGGGAGGCGGCGCCGATCTCGGCGGTGCGGCCCCAGCCGAGGACCTTCGCCACCGTCCCCGGAGCCGGGTCGGCGGACGCGAGCGGCAGCACCCGGTTCGCGACCGGCCTGACCAGGGTGAGCACGGCGACGTCGCTGCCCTGCTCGGCCGACGAGTAGAACGGGTGCTTCCAGATCCGGGCCACCCGCAGCGTCTCACCCGCCTGGGTGCGCTTGTCCTCGCGCCCCGCGACGACGACGAGCCGCTCCGGGGCGGTGCCCGCGACGCAGTGCGCGGCGGTGACCACCTTGGTCGGCGCGACGAGCGTGCCGCCGCAGAACTGGCTCCCGGTCGTGCCCGCCAGGAACACCACCCACGGGTGCTCGGCGATGGACGCGCGCGTCCCGCCGACGACTCTCGGTTCCGCCGCGGTCGCGACGCCCCCTCCGCACAGCACCGCGAGAACGCTGAGAAAAACGGCAAGCCTCATCGCCCCTCCTACGCCTAGTGGGGAGCGCCCGAGTCCGAGCACCCGCGAGGAGGTTAGCCCTGAAAGAGCAGGTCGATGCGCCGAAAGGAGCACACGACCTGGTCGGCCCAGCCGCGCGACCCGGCTGTCGCAGCGGCGGGCCCGCCGGGTCGCGCCGCGTGCTGTCGATCAGTTCCCGGAGGGTGAACCGAAGCCGGAGAAGCGCCCCCTGACCTTGCCCGCCGCGTCCGCCACGACCCCGCCGAGGTCGTTGACGACCTTCATCAGCGGGTCCTCGGACTCGGCGGCGTCGGACTTGTAGGAGCGGGCCGCCTCCTTGAGGTCCTCGGTGAACGTGCTGGACGCGTGGTCGTCCTCGCGGCGCCGGTAGTCGCCCGACAGGATGGCCCGGTACTCCTCGCTCGCGGCCCAGCGCTGGAGCTCGGCGGCGCGCACCACGGCCATCGGGTGGGTCAGCGGCCAGGTGCGGATCAGCTTGAGGACGCTGTCGCGCACGTCCTCGACCTGCTCGTACTCCTTGGCCTGCTTGAGGAACTCGGCGGTGTCGACCTGGGTGAGGTCCATGCCGCCCGCGAGGGCGACGTGCACGCGCAGCGCGGCGGCCGGGTCCTGGGCGCACAGCAGGCCCGCGCGGTCGCAGCTCAGCTCGGTCTTGCGGTACCACTCGTGCAGGGCGGCGATGACGGCGCGGACCGCCCAGTAGCCCGCGGGCATCCAGCCGAGGCTGTGCTGGAGCTGCATCAGCCGCATGAGGATCGTCTGGTAGAGCGCGTGGCCGGAGAGCACGTGGCCCATCTCGTGGCCGATGGCGAAGCGCAGGCCGTCGTGGTCGAGCAGGTCGACCAGGCCGGTGGTGAGCACGATGAACGGCTTGTCGATGCCCAGGGCCATCGCGTTCGGCTGCGGGTTGCGGGTGATGAACAGCTCGGGGACCGGGTCGAGGTCGAGCGTGGCCGCGGTCTCGTTCCGCAGCCGGTCGAGGGCCGGGTACTGCTTCGGGCCCACCCGGATGGAGGTCGCCAGGTAGCCGAGGCGCTCGCCGCGCTCGGTGAAGGCGCCCGCGACGGACTTGAGGACCGGACCGATGCCGGGGACCGCGCGCAGGACCGCCAGCGCGCCCCGGTCGACCGGGTGCTCGTAGGCACGGGGGCTGATACCGGGGAACCGAACCCTGGAGGTCGACCGCTCGATCTCTTCGCTCATCCTCCCAGCGTGCCACGCCCCATTTCCCCCTACTCCCCGTTCGGGGGAATCACGGGCACACTGACGGGGTGGAACCGGATGTGCTGGGCGACGGGTTCGAGGTCAGGACGCTGCCGCTGGGCTCGGAGGCGAGCGCGGCGCTGGTGCGCAGGCGCGCCGACGGGGCGGCCGAGCGCGGGGCCGTGCTGTACGTGCACGGGTTCGCGGACTACTTCTTCCAGCGGCACGTGGCCGAGCACTTCGCGGCGCTCGGGTACGACTTCTACGCGCTGGACCTGCGCGCCTACGGGCGGTCGCTGAGGCCGGGCGAGGTGGCGAACCACGTCGAGGACCTGTCGACGCACTTCGAGGAGCTCGACGCCGCCGTGCGGGTGGTGCGCGAGGAGGACGGGCACCGGGGGCTGGTGGTGGTCGGGCACTCCACGGGCGGGCTGACCACCAGCCTGTGGGCGCACGAGCGGCGCCTGGACGGCGCGCTGGACGCGCTGGTGCTCAACAGCCCGTGGCTGGACCTGGCCGAGCCGTGGGTGGTGCGCACGGTCGGCACGGCGGTGGTGCGCGGGGTGGGGCGCCTCGCGCCGAAGCTGGTGCTCAAGCCGGGCCTGGGGCCGGTGTACGGGCAGAGCATCCACCGGGACCACCACGGCGAGTGGGAGTTCGACACCGCGTGGAAGCCGATCGAGGCGTTCCCGGTCACGGCCGGGTGGTTGCGGGCGGTGCGGGTCGGGCACGCGCGGCTGCACCGGGGGCTGGACGTGCGGGTCCCGGTGCTGGTGCTGCACTCGGCGCGCAGCCACCTGAAGGCGAGGCGGTGGTCGGCGGAGGCCATGACGGCGGACGCGGTGCTGGACGTGGGGCACATGCGCCGGTGGGCCCCGAGGATCGGCCGGGACGTGTCGCTCGTCCAGGTGGAAGGGGGGATGCACGACCTGTTCCTGTCGGCCGCCCCGGTGCGCGAGAGGGCACTGGCCGAGGTGGACGCGTTCCTGGAACGTAAGGTCGAGCGGTGACCGTTCCCGACCCGAACCAGCTGCACCCGATGGCCGATCACCCGAGGGTGGTGCTGCTCAAGCCACTGGTCGACGCACCGAACATCGAGGTGGGCGACTACACGTACTACGACGACCCCGAGCGCGCGACCGAGTTCCAGACCCGCAACGTGCTGTACTCCTACGGCCCGGAACGCCTGGTCATCGGCAAGTACTGCGCTCTGGGCACGGGCACGACGTTCATCATGGCGGGCGCGAACCACCTCACGAGGGGCCCGTCCACGTTCCCGTTCACGATCTTCGGCGGTGCCTGGGCGGAGAAGACCGCCGACATCATGGCCGCCGCCCCCAGCAAGGGGGACACGGTCGTGGGCAACGACGTGTGGTTCGGCTGCGGCGCCACCGTCATGCCGGGCGTGACCATCGGTGACGGCGCGATCATCGCGACCGGCGCCGTGGTGACCTCGGACGTCGCCCCGTACACCGTCGTCGGGGGCAACCCGGCGCAGGCCGTGCGGCAGCGCTACCCCGACGACAAGATCGAACTGCTGCTGCGCGCGGCGTGGTGGGACTGGCCCGTCGAGCTGGTCACCGAGCACGTGCGCGAGATCATGGCGGGCAAGGTCAAGCAGCTCGCCGAGATCGCGGAGGAGAACGGGCTGCTGGGGCCCAAACCGCGCTAGCGGCAGGACAGCTTCCCACCGGGGGCCGGGTTCCGATCGGAACCCGGCCCCCGTCGGCTCAGGCGGCGGTGGTGGCCGCCGCGGCCTCGGGCTCCAGCGCCAGCGCCAGGACCTCGCGCACGTCCCCGACCAGGTGCACGGTCAGCGCGTCCCGCACGTCCTGCGGGACCTCCTCCAGGTCCGGCCCGTTGCGCGCGGGCAGCAGCACGGTCGTGATGCCCGCCCGGTGCGCGGCGAGCAGCTTCTGCTTCACCCCTCCGATGGGCAGCACCCGTCCGGTGAGGGACACCTCGCCGGTCATCGCCACGTCCGAGCGCACCGGGCGGCCCGACAGCAGCGACGCGAGCGCCGACACCATCGTGACGCCCGCCGACGGCCCGTCCTTGGGCACCGCGCCCGCCGGGACGTGGACGTGCACGCCGCGCCCGTCCAGGGTCGCGGCCCGCTCGTCGTGCGCCCGCAGGTAGGACAGGGCGATCTGCGCGGACTCCTTCATCACCTCGCCGAGCTGCCCGGTGAGCACCACGCCGGACGCCCCGGTGCCGGGTTCGGCGAGCGCGGCCTCCACGAACAGCACGTCGCCGCCCGCCCCGGTCACCGCCAGTCCCGTGGCCACGCCGGGGACGGCGGTGCGCTCGGCGGACTCGGGGGTGAACTTCGGCGACTTCAGGTAGCCCTCCAGGTCGCCGCCGTCCACGGTGACGGGCAGCTCGGCCCGGTCCAGCGCGACCCCGGCGGTCACCTTGCGCAGCACCCGCGCGAGCGAGCGCTCCAGCTGCCGCACCCCGGCCTCGCGGGTGTACTCGCCCGCGAGCCTGCGCAGCGCGGCCCCGGTGACCTCCACGTCGCCCGGCTCCAGCCCGGCCCGCTCGACCTGCCTCGGGAGCAGGTGGTCGCGGGCGATGGTGACCTTCTCGTCCTCGGTGTAGCCGTCGAGCCGCACCAGCTCCATGCGGTCGAGCAGCGGGCCGGGGATGGACTCCAGCACGTTCGCCGTGGCCAGGAACACCACGTCGGACAGGTCCAGCTCGACCTCCAGGTAGTGGTCCCGGAAGGTGTGGTTCTGCGCCGGGTCCAGCACCTCCAGCAGCGCGGCGGTCGGGTCGCCCCGGTGGTCGGCGCCGACCTTGTCGATCTCGTCGAGCAGCACCACCGGGTTCATCGAGCCCGCCTCGGAGATGGCGCGGGCGATGCGGCCGGGCAGCGCGCCGACGTAGGTGCGCCGGTGGCCCCGGATCTCCGCCTCGTCGCGCACGCCGCCGAGCGCGACGCGGACGAACTTGCGGCCCATGGCCCGCGCGACGGACTCGCCGAGCGAGGTCTTGCCGACGCCGGGCGGCCCGACGAGGGCGAGCACCGCGCCGCCGCCGCGCCCGCCGACCAGGCCCATGCCCCGGTCCGCGCGCCTGCGCCGCACCGCCAGGTACTCGGTGATGCGCTCCTTCACGTCGTCCAGGCCCGCGTGGTCGGCGTCGAGCACGGCCCGCGCGCCCGCGATGTCGTAGGAGTCCTCGGTGCGCTCGCCCCACGGCAGGTCGAGCACGGTGTCGAGCCAGGTGCGGATCCAGCCGACCTCGGGGGACTGCTCGGAGGTGCGCTCCAGCTTGTCGACCTCGCGCAGCGCCGCCTCCCGCACCTTCTCCGGCAGCTCGGCGGCCTCCACGCGGGCCCGGTAGTCCTGCTCCTCGGTGGCGGGCTTGCCGTCCAGCTCGGCCAGCTCCTTGCGGATGGCGGCGAGCTGCTGGCGCAGCAGGAACTCCCGCTGCTGCTTCTCCACGCCCTCCTTGACGTCCTTGGCGATGGTCTCGGCGACGTCCAGCTCGGCCAGGTGCGCCCGGCCCCACTCCAGCAGCCGCTCCAGGCGGTCGCCGACGTCGCCGGTCTCCAGCAGCCACACCTTCTGGTCGTTCTCCAGGTACGGCGCGTACCCGGCCAGGTCCGCGAGCGCGGAGGGGCCGTCGACCTGGCGGACGGAGTCCACGACCTGCCAGGCGCCGCGCTGCTGGAGGATCGTGGTCACCACCGCGCGGTAGTCGCGGGCCAGGGAGTGCGCGCGCTCGTCCGGCGGCGGCTCCTCGACGACGGTGGCCTCCACCCACAGCGCGGCGCCGGGCCCGGTGGTGCCGGTGCCGATGCGCACCCGCTCCGTCGCGCGCAGCACGGCGGCCCGCTCGCCGCCCGCGAGCCTGCCGACCTGCTCGACGGTGGCCAGCGCGCCGACCTTCGCGTAGCGGCCGTCCAGGCGGGGAACCAGGAGCACCCGCGCGCCGTTCACCCCTCCGGCGGCCGAGGTGGCCGCCTCGACGGCGGCCCGCGCCTCGGCGCCCGCGTCCGAACCGGTCAGGCGCACCGGGACGACCATGCCCGGCAGCACGACGGTGTCGTCGAGGGGCAGGACCGGGAGCGCCAACGTGTCACCCATGCGAAGCCTCCAGAGTTGAGTCTGACAGGCTCAACCGAGTTGAGTCCCCGGTTGTTTCCGAGTTCTGTTCGCCCAGAGCGAGACCGAGGAGTTCCGCGCGCGGGGCTTGTGCGCGGCGACCGGGGTTCGACACGATCGGCGGTTCCACCCGGTCAAGAGGAGAAGGCTTTTATGGAGCAGGCGAGCTGGGTCCCCGCGTCGGTGGACCTGGACCGACCGAGCACGGCCCGGATGTACGACTACTACCTGGGCGGGTCGCACAACTTCGCCGTGGACCGGGAAGCGGCCAAGGCCGTGGAGCACGTCTTCCCCGGCATGTCCGGGGCGGCGCGCTCGCTGCGGACGTTCCTGCGGCGCTCGGTGCGCTACCTGCTGGACCAGGGCATCGACCAGTTCCTGGACCTGGGCTCGGGCATCCCGACCGTGGGCAACGTGCACGAGATCGCCCAGGCCGCCAACCCGGCGGCGCGCGTGGTCTACGTGGACATCGAGCCCGTCGCGGTCGCGCACAGCACCGCGATCCTGTCGGCGAACCCGCTGGCCACCGCCATCCAGGCGGACCTGCGCGACCCGGCGTCCGTGCTGGAGAACGAGGACGTGCGGCGGCTGCTGGACTTCGACCGGCCGATCGGCGTGCTGATGGTCGCGGTGCTGCACTTCGTGCCGGACGCCGACGACCCGCACGGCGCGATCGCCCGGTACCGGGACGCGCTGGTCCCCGGCAGCTTCCTGGCGATCTCGCACGCGACCGTGGAGGGCGTGCAGGTCGACGCCGAGCAGGACACCGCGCGGGTGCAGGACGTGTACAAGCGCACCGAGAGCCCGCTGATCTTCCGCGACCGGGCCGAGGTGACCAAGCTGTTCGACGGGTTCGAGGTGGTCGAGCCGGGCGTGGTGCCGCTGTCGGAGTGGCGGCGCGACTCGGACGACGCCTACACCAGCGCGTACGTGGGCGTGGGCCGCAAGGTCTGACCCGGCGCGGTCGCGGCGGGGCGCCCTGGGCACCGGGCGCCCCGCCCGATCACGTCACCCGCCCAGGGACCCGTTCACTCGGCCGGGTTGAGCCGCAGGTCCGGGTTCACCGGCGGCGCCCCGTCGAACGGGCCGGGCACCAGGCCGCCGAGCTGGTCCAGGGTCAACCGCACGTCGGCCGCGAACGGGTCGGTCCCGGCGGGCGGGTCCGCGAACCAGGACTTCAGCTCCTCCGGCACCGGGTAGCCGTCCGCCAGCTCCCGGTACTGCTCGCCGCGCTCGCGCGCCTGCCTGGCCAGCTCCTGGTACTCGCGCATGGCGATCCGCATCCGGATCCACCGGTACCGCGCGGTCCGCTCGCCGCCCTCCTGGGTGAACCTGGTGCGCAGCAGCTCCCCCGCGACCCGGCCGCGCTCGGCCAGCGCCCGGATCGTCTCCGGCCGCATGAACAGGTTCGTGCCGCCCTCGCCGCCGCGCAGCCGCACGTGCGCGATCCGCCCGCGGAAGCCCGGCAGCGCCGACTGCATCGCGTCCCGCCAGCCGAGCGCGGTGTCCAGGACCGCCTGCGCGAACCCGACCGCGCCGGTGACCGCCCGCCACGGCCTGCCCTCCTGCGAGGCGTCCTGCTCGGGCAGCCACACGTCCGGCGCGTCCGGCGCCGGGTAGCCCTGCAGGGTGAGCCCGAACGTGGGCCAGCGGGGCAGCAGGGTGTCGAAGAAGTGGATGGGGAAGTTGCTGGTGATGCCGCCGTCCGAGAACCAGTGCACCCTCGGCTCGGGGTCGGCGCGCACCAGCGGCACCGCCGAGATCAGGCCGGGCATCGGCGTGCTCATCCGCACCGCGAGCGCCACCGGCAGGTCGGCGGGCAGCACGCGCAGCGCGGTCGCCGGGTGCAGCGGGCAGCGCGCGTCGTCCGCGCCCTCGTCGCCGAGCAGGTCGACCACCCGCGCGGGCAGCACCGCCGCCAGGCAGTCGGCGCAGAACAGCCAGCGGTCGTCCGAGGTGAACGGCAGCCTGCACGGGCGGCCCTCGGAGACGTCGGTGCTCATCAGCACCAGGTTCGTGGTCAGGTCGGAGAAGCGCAGCCCGCGCACGCCCGCGAGGTGGTCGAGGGAGTCGGCGAGCCAGTCGCTCAGCGGCGGGACACCGGTGGACTTCGGCATCCCGCAGCGGCGGTCCCACCAGCTCGACCGGTAGCCGCCGGTGCCGGGCACGAGCCCGAAGCCGATGGACGCGGCCCGCTCGCGCACGAACCTGCGCACCCCGCCCGCGTAGATCAGGACGACCGCGCTGGCCAGCCCGAAGCCGAGCACCAGCCACACCACGCCCGCGGTGGCGGCCGACGCCAGCACCGCCCAGTCCGCGCGCAGCCGGGGGACGATCGGGTAGAGCGGGACGGCCGCCAGCAGCAGCAGGCCGATCCGGGCGGGCAGCGGCCCGCGCCCGCTGGGCAGCGCCTTCGCCGCCACCCACGGCACCGCGAGCACGGCCACCACCACGATCGCCGCCAGCCCCCAGGTCGGGAAGCCGGGCCAGGCGACCGCGCCGAACCACAGCACCGGCCCGGCCAGCCAGACCAGCAGCGCCGCGGCGAGCGCGGCCTTGGCCCGCAGGCCGATCGCGCCCAGCAGCGCGAACACCAGGGAGACCGCCGCGCTGCGCCCGGTGGTCTCCCGGCTCTGCATGGTCGCGGTGACCAGCCGGTAGAGCTTGCGGGTGGCCCTGGTCGGCTGGAACAGCTGGGCGAGCCGCTGCTGCCCGGCCGCGAACCAGGAGACCGTGTCGGCGAGCCGGTCGAACCCGCCGCTGTCCCGCCCGCGCTCGGCCGCCGCCGCGAACGAGGCCCCGATCGCCCCGGCCGAGGCCCCGCCGAGCGAGCGGAACCGGTAGTGCTTGGACAGCTCGACCACGGCCAGCGGGTAGACGATCCCGCTCGTGGCCCCGCCGCGCATGGTGAGGTCGCAGCACCTGTCGAAGTCCTCGTCGTCCCCGTCGTCGCCTGCCGCCATCACCGGATGGTCCCGCGCGGTGCGGGGTGCGCCGCTAGGGCTGATCCGGGGAAGGCGCGCGGGTGGAGCAGTCGTGCGCCCCACCCGCCGACGCCGTCCGGTCAGCGCCGTCCGCTCAGTGCCGTCCGGTCAGCGCCACCCGCTCAGCGCCGCTCGCTCAGTGCCGCTCGCTCAGTGCCGCTCGCTCGGCGGCGCGAGGAAGTCGTCCAGCAGCACCGGGGTCATCCCGTCCGCCTTCGCGCGCTCGCAGAACGCGGTGAAGTCGGCCACGAAGCTGTCCCGGAAGTGCATGAGCACGATGTCGCCGCCGCGCAGCCTGTCCCCCACCTGGAACTGCACCACGCCGTCGTTGACCGCCGCCGTCCACAGCACCACCGCCCGCATCCCGCACGAGGCGGCGGCGCGGCGGGTGTTCAGGTCGTAGTTGCCGAACGGCGGGCGGAACAGGGTCGGCCTGGTCCCGAGCGCCGCCCCGAGGTGGTCGGCGTTGCCGCAGATCTCCGCGCGCTGCGCCTCGTACCCCATGCCGCGCAGGTTCGGGTGGTCCGTGGTGTGGGCGTGCACGTGCGCGCCCGCGCCCCGGAGCGCGTTGAAGTACGCCGGGTCCGGCTGCACGTGCGTGGTGTTGAGGAACAGCGACGGCTCGATGCCGGAGTCGCGGATGAGCTGGAGCGCCTTGGGGTGCCGGACGGCCCCGTCGTCGATGGTCAGGAACACGTAGGGCTTGTCGGTCTCGATGCTGCTGACCACCGGCGCCAGGTCGCCCTCCTGCGGCGGGGCCTCCTTCTGGGCCGTGCCGTACCGGTAGGGCTGCTGGAACAGCTTCGGCGGCGGCGGGGGTGGGGTGGTGGTCGTGGAGGTGGTCGTCGTGCTCGGCGGCACGGGCGCCGCCTCGGGGGCTTCGGGAGCAGGCGAGCAGGCCGCCAGCAGTCCCAGGGCAGCCGTCATCGCTACTGCCAACGCGCGCATGGAGTGGATCCCCCCGGAGGATTGCTTTTCCTCCGGATGAGACGCGGGCGCCGCCATCCGGGTTGCACGGCGATCGCGAACCGCCGGGGATAGGGTCGGGCCCGACAGCCAAGATCACCAGCGGAGGACCCGATGAGCCTCGACCGACCCGTCGCGCCGGACCCGTACTCGCTGCTCCCGACCGCTCCCGCGTTCCAGGTCACCTCGACCGACGTGGCCGACGGGCAGCCCCTGCCGCAGGCGCAGGTGTTCGAGGGCGGCAACACCTCGCCGCAGCTGTCCTGGAGCGGGTTCCCCGAGGGGACGAAGAGCTTCGTGGTGACCTGCTTCGACCCGGACGCCCCCACCCCGTCCGGCTTCTGGCACTGGGTCGCGGTGAACCTGCCGGTCTCGACCACCTCGCTGGACACCGGCGCGGGCGCGGACGACGACTCGCTGCCCGGCGGCGCGTTCCACGTGCGCAGCGACTACGGCACGCGCGCGTTCGGCGGCGCGGCCCCGCCCAAGGGCGACCGCCCGCACCGCTACTTCTTCGTGGTGCACGCGGTCGACGTCGAGGCGCTGGACGTGGACGGCGACGCCTCGCCCGCCGCGGTGAGCTTCAACCTGGCGTTCCACACCCTGGCGCGGGCGATCATCACGCCGACCTACCAGCACTGAGCGGCGGGAACATCCGCCAGGACGAGAGGGTTGAGCAGGGCGTGAGGCACTTCGACCTGGTTGTCATCGGCACCGGCTCCGGCAACTCCATCGTGGACGAGGCGTTCGCCGCCTGGGACGTCGCGATCGTGGAGAAGGGCGTGTTCGGCGGGACCTGCCTGAACGTGGGCTGCATCCCGACGAAGATGTTCGTGCACACGGCCGACCTCGCGGCGGGTCCGGCGAGCGCGGCCCGCTTCGGCGTGGACGCCTCGCTCGACGGCGTGCGCTGGACCGACGTGCGCGACCGGATCTTCGGGCGCATCGACCCGATCGCCGAGGGCGGGAGGCGGTGGCGCGAGAGCGGCAGCGCGAACACCACCGTGTACAGCGGGACGGCCCGGTTCACCGGCCCCAAGACGCTCGACACCGGCGCAGGCGAGACCATCACCGCCGACCGGTTCGTGATCGCGGCGGGCTCGCGCCCGGTCGTGCCGGACGTGCCGGGCCTGGTCGAGACCGGCTTCCACACCAGCGACACGGTGATGCGGCTGGACCGGCTGCCCCGGCGGATGGTGATCCTGGGCAGCGGGTTCGTGGCCACCGAGTTCGCGCACGTGTTCTCGTCGTTCGGCGTGGAGGTCACCCTGGTGGCCCGCTCCGGCGCGCTGCTGCGGGCCGAGGACGACGCGGTGTCGGCCCGGTTCACCGAGCTCGCCTCGGCCAAGTGGGACGTGCGGCTCGACCGGCGCGCGGTGCGGGCCGAGCGGGTCGACGGGGTGGCGCGGCTGCACCTGGAGGGTCCGGACGGGCCCGAGGTCGTGGAGGCCGAGGAGCTGCTGGTCGCGGTCGGCCGTCAGCCGAACGCGGACCTGCTGGACGTCGCGGCGACCGGGGTGGCCCTCAACGACAAGGGCAGGGTCGCGGTCGACGAGTTCCAGCGCACCTCGGTGGAGGGGATCTACGCGCTGGGCGACATCAGCTCGGACTACCAGCTCAAGCACGTGGCCAACCACGAGGCGAAGGTGGTGCGGCACAACCTGCTGAACCCGGACGCGCCGATCGCCTCGGACCACCGGTTCGTGCCGTCGGCGGTGTTCTCGTCGCCGCAGATCGCCTCGGTCGGGCTGACCGAGCGGGACGCGGTGGCGAAGGGCGTGTCGTACGTCAGCGTCGAGCAGCCGTACGCGTCGATCGCCTACGGCTGGGCGATGGAGGACACCACCGGTTTCGTGAAGCTGCTGGCCGACCCGGTGACCGGGCAGCTGCTGGGCGCGCACGTGATCGGGCCGCAGGCGCCGACCGTGGTGCAGCCGCTGATCCAGGCGATGAGCTTCGGCCTGGACGCGCGGTCGATGGCCAAGGGGCAGTACTGGATCCACCCAGGGATGCCGGAGGTCGTGGAGAACGCGCTGCTCGCGCTGCCGCTCAAGGACGCTTAGGACTCGCGCGGCACGGCGGGAGGCCCGGACCACGTCGGTCCGGGCCTCCCGCTGTTCCGGGGGTGTCAGATGGTGCGCGGCCGTCCGGCGATCACGCCCAGGGCGATGAGCGCGACGAGGATGCCCGCGAGGACGTACATGGACACCGTCCACGCGCCGGTCACGTCGCGCAGCACGCCGAACGCGAACGGTCCGGCGGCCGAGATCAGGTAGCCGATGCTCTGCGCCATCGCGGACAGCTTCGCGGTGTCGGCGGCGGTGGCGGTGCGCAGCGAGATGATCACCAGGGCCAGCGGGAACACGCACATGCCGGTGCCGATCAGCACCACCCACAGGCCGGGCGCGGCGACCGGCGCGATGGCCAGGCCCAGGATGCCCGCGATGGACAGCGAGCCGAGCAGCACGACCAGCCAGGACTGCGAGCCCCAGCGGGTGGCCAGCGGCGGCACGACGAGGCTGACCGGGACGCCGAGCACCATGGTGATCGCCAGCAGCATCCCGGCGGTGGTCCGGTCGACGCCGGAGTCGGCCATGATCTGCGGCAGCCAGCCCATGACGGTGTAGGCGAGCAGCGACTGGAGCCCGAAGAAGACGGTGATCACCCAGGCCAGCGGGCTGCGCAGCACGGAGGTGCGGCGCTGCTGGACGGGGTGGGCGCCACGGGCGGGCGCGGCGCCGGAGGCGGCGGGGACTGCGACAGCGGGGGCCGCGCCGTGGCGGGCGCTCGCGGACCACACCAGCAGGGCGGCGGTCGACAGCAGCGCCCAGGTGGCGGCGGCGAGCTGCCAGGAGCCGAGCGCGGTCTCCAGGGTCGGGGTGAGGGCGGCGCCCACGGCGGCCCCGGCGGCGAGCGCGGCGGTGTAGACGCCGGTCAGGAACCCGACCTTGTCCGGGAACGACTCCTTCACCACGACCGGGATCAGCACGTTGCACACCGCGATGCCCGCGCAGGCGGTGAACGTGCCGCCGAGCAGCACGGCAGGGCCGTCCAGGACCCGCAGGACCAGGCCGAGGGTGAGCACGACCAGCGACGCGCCGACCGCGCGGGCCATGCCGAAGCGACGGCCCAGCCACGGGGCGGCGAACGCGGCGACGCCGAAGCAGACGGTGGGCACGGCGGTCAGCAGGCTGGTCCACGCGGTGGTGGCGCCGAGGGAGGCGCGGACGTCGCCGAGCACGGAGGCCAGGCTCGTGACGGCGGGGCGCAGGTTCGCGGCGGCGAGCGCGACGCCGACCGCGAGGAGGGTGCTGCCGACCAGCGCGGCGCCCCGGTTTGGCCGCGGTGCGGGGGCGGGTTCGGCCGGGGGCGCGGTGGCGGGTGCGGCAGTCGTCGGATCAGCGGTGGTCTGATCAGCGGCTCCGGTGACCGGATGTGTTCCCACCGTCGCGTCGTCACCCGGATCGGTGGCAATGTGGACGGACACGGGAATTCGGTCTGGCGGGATTTGCTGGATCGACACTCGGTTACTATCGCAGACATAGGATGTTTGGATGAAAGGATGCCGCTGTGCCGTTGGCCACTACTCGACGGGCGGGCCTCGTCGACCAGGTGATCGACCAGATGAGGGGGGCGATCGCCAGCGGTGAATGGCCGGTCGGCCGGCGCATCCCCCCGGAGCCGGAGCTGGTGACGGCGCTGGGCGTGGGGCGCAACACCGTGCGCGAGGCGGTGCGGGCGCTGGCCCACGCCGGGCTGCTGGAGGTCCGCCAGGGCGACGGGACGTTCGTGCGCGCCACGAGCGAGCTGTCCGGGGCGGTGCGCAGGCTGTGCGGCAGCGAGCTGCGGGACGTGCTCCAGGTGCGGCGGACGCTGGAGGTCGAGGGCGCGCGGCTGGCCGCGACCCAGCGCACCGAGGAGGAGCTGGCCCGGCTGGAGGTCGCGCTCGCCGAGCGGGACTCGGCGCTGGCCGCGAAGGACTGGGAGCGGCTGGTCGAGCGGGACGCGCAGTTCCACGAGCTGCTGCTCCAGTGCTCGCACAACACCCTGCTGGCCGAGCTGTACCAGGGCCTGACCGAGGCGGTGCGGGCCAGCATCGACGCGACCGTGCGCACCGCGCCGGACGACGACGACCTGTCCCACGAGGGCCTGCTCCAGGCGATCCGCGACGCCGACCCGGCGCGGGCGGCGCTGGAGGCGGGCGGGTTCCTGGAGGAGCTGCTGGAGCGGCACGGGGAGTAGCGGGCGGCGGTCGCCCACGAGGGGTTCGCGCGCACGGGCGGGAGCGCCGCGCGCGGATCACCCGCGCGCGCTCTCACCGCCGCGCCGGGACCACCGCGCTCTCACTGCGGCGCCGTCACCCCCGCGCCGTCATCCCCGCGCCGTCATCCCCGCACCGTCAACGCTGCGCGATCACCCCCGCGCCGTCACCGCCGCGCCATCACCCCCGCGTCGGGACCCACGCCTCCCAGACCTCCCGCAGCACCTGCGCCACGGCCCCGATCGCGGGTCGCCTGGCCGCCTGCGCGCGCCACACCACGAACACCCGCCGGGTCGGCCGGGGCTCGAACGGCACCGCGCGGACGCCCTCCGGCAGCGCGCCCCTCCCCAGCCTGGGCAGCAGCGCCACCCCCACCCCGCGCTCCAGCAGCGCCAACTGGGTCTCGTACTCGCCGACCCGGTGCGCCAGCAGCGGCTCGACGCCCTCCGCCCGGAACGCGTTGACCAGCCAGTCGTGGCAGATCGTCCCCTCGGGCTGGCAAATCCACCGCTCCCCCGCCAGGTCCGCCACCCCGACCGCCGCGCGCCCGGCCAGCCGGTGCGCCGACGGCAGGAGCACGTCCGCGTAGTCCTCCCCCAGTCGCACCCGCGCCAGCGACTCGTGCACGGGCAGCGGCGCGTTCACCCAGTCGTGGGCCACGGCCAGGTCCAGCTCACCGCGCGCCACCGCGCCGATCGCCTCCGGCGGGTCCTGCTCGACCAGCCGCGCGTCCAGCTCCGGGTGCCGCACCGCGAGCTCCGCGAGCGCGGGGGGCAGCAGCCCGCGCGCGGCGGTGGAGAACGCGCCGATCCGCAGCTCCCCCACGACCTGCCCGCGCTGCCGCTCCAGCGCCACCTCGACCCCCTCCACCAGGGCCAGCACCCGCTCGGCGGTGTCGGCGAGCAGCAGCGCCGCGTCGGTGAGCACCACCCCGCGCCCGCGCCGCTCCAGCAGCACCGCGCGGGTCTCCCGCTCCAGCTTGGTGATCTGCTGGGACACCGCCGACGGCGTGTACCCCAGCGCCGAGGCCGCGGCCCCGACCGAACCGTGCCGCGCCACCGCGTGCAGCGCCCGCAGGCGTCCCAGGTCGAGCATTCAGCAATGCTAAACCCCACGCTTCAGAACTTAGCTCTGGTGCTAAACGATTGGCCGGGCTGAGACTGGCGGGCGTGAAACCAGCCCACTCCGCCGTCGCGGTGCTCGTCGCCGTCATCTGGGGCGTCAACTTCGTCGTCATCAAGGTCGGCCTCGCCGAGTTCCCGCCACTGCTGTTCTCCGCGCTGCGGTTCCTGCTCGCCGCCGTGCCCGCCGTGCTCTTCCTGGGCGGGCCGCGCGTGGCGTGGCGGTGGGTGTTCGGCGTGGGGCTGGCGCTGGGCGTGGTGAAGTTCGGCCTGGTGTTCACCGGGATGCACGCCGGGATGCCCGCGGGCCTGTCGTCGCTGGTGCTCCAGAGCCAGGTGGTGTTCACCGTGGTGCTGTCGGCGGTGGTGCTGGGCGAGCGCCCGCGACCGGCGCAGGTGCTGGGCCTGGCGGTGGCCACGACCGGGTTCGTGGCGATCGCGCTGGACTACCGGGTGTCGAGCCCGGTGTCGGCGCTGCTGCTGGTCGTGGGCGGGGCGCTCGCGTGGGGCGTGGCGAACGTGCTGACCCGCAAGGCCCAGCCGCCGGACTCGCTGCGGTTCATCGTGTGGGTGAGCGCGGTGGCCGTGCTGCCGCTGCTGGCGCTGTCGCTGCTGGTCGAGGGCCCGGAGGCGGACCTGGCGGCGCTGCGCGGCGCGGACTGGGCGGGCGTCGGGTCGCTGCTGTTCGTGGCCTGGGGGTCGACGCTGCTCGGCTTCGCCCTGTGGGGCTTCCTGCTGCGCACCTACCCCGCGCCGCGCGTGGTGCCGTTCGCGCTGCTGGTGCCGGTGGCCGGGATGCTGTCCGGCTGGCTGCTGCTGGACGAGGAGGTCACGGCGGTCCGGCTGGGCGCGGCGGCGCTGGTGGTGGCGGGCATGGGGGTGGCGACGCTCACCCGCCCGCGCCGCCGCGCCGAACCGGTCGTGGCGGCCGTGCCGGTGTAGCCCCCGCTCAGGAGCTCGGCCGGATCGCCCCGCGGTGGGCGGTCCGGCCGAGCGCCGCGCACGGCGCGGGCCGACCGTCCGCGCCCGGCGCCCACGCCCCGGCCCGACCACCGCAGCCCGCGCTCACCCGACCGCTGGCGCTCCCGCGGGCGGCACCACACGCAGCCCACCCGGCACCCCGCGCTCCAGCAGCGCCCGCACCGCGCCCGTGTCCAGGTGGTCCACGACCAGGTCGCCGAGCAGGTCCAGCTGGGCCTCGCGGCGGGCCGCGAAGTCGGTGTCCGGGGCGACCGCGAACCCGTCCCGCCCGGCGAGACCGGCCACGTGCCGCAGGAACGCCCGCCGGAACGCGTTGTTCTCCAGCAGCCCGTGCCAGTGCGTGCCCATGACGCGCCCGCGCACCGCGCCCTCGACCTCGCCGTCCGGCAGCTCCACCAGCCCCGGCAGGTCGTCGGCGCGGCGCGCCACCCGGCCGTGGTGGATCTCGTACCCGGTCACCGGCTCGCCCAGCGCGACCCCGGTCGGCCGGTGCAGCGCCTTCTCCGGCTCGAACACCACGTCCACGTCCAGCAGCCCCAGCCCCGGCACCGCGCCCGCGCCGGACTCCACCGGGTCGTCGATCGAGCGCGCGAGCATCTGGTAGCCGCCGCACACCCCCAGCACCGGCCCGTCGTGCGCGGCGATCGCGTCGGCCAGCCCGGTGCGGCGCAGCCACGCCAGGTCCGACACGGTCGCCTTGGAGCCGGGCAGCACCACCAGGTCCGCGTCGGCCAGCCGGGACGGCTCGGTCACGAACCGCACGGACACGCCCGGCTCGCAGGCCAGCGCCTCCACGTCGGTGGCGTTGGAGATCCGGGGCAGCCGCACCACGGCCACCCGCAGCCACTGCCGCCCCACCGGGGCCTGCGGCCTGCCGATCACCCCGTCGGCCGCGTAGGACAGCGAGTCCTCGGCGTCCAGCCACAGCTCCTCGCGCCACGGCAGCACCCCGTGCACCGGCCGCCCGGTCAGCTCCCGAAGCTGCCGCAGCCCCGGTTCGAGCAGCGCCGGGTCGCCCCGGAACTTGTTGACCACGAACCCGGCCACGAGGGCCTGGTCGGCCGGGTCGAGCAGCGCGAGGGTGCCGAACAGGTGCGCCAGCACCCCGCCCCGGTCGATGTCGCCGACCACCAGCACGGGCAGCCCTGCGGCGCGCGCCAGCCCCATGTTGGCGATGTCGGTGGCCCGAAGGTTGATCTCCGCGGGGGACCCGGCGCCCTCGCACACCACGGCCTCGTAGTCGGCGCGCAGCCCGGCCAGGGTGTCGAGCACCACGGTCATCAGCTCGGCCTTGCGCTCCCGGTAGGACATCGCGGACACCTCGCCCGCGACCTTGCCCAGCACCACCACCTGGGAGCTGCGGTCACCACCGGGCTTGAGCAGCACCGGGTTGAACCGCACGCTCGGCTCCAACCCGCACGCGGCGGCCTGGAGGGCCTGCGCGCGGCCGATCTCGCCGCCGTCCGGGGTGACCGCGGAGTTGTTGGACATGTTCTGCGCCTTGAACGGCGCGACCCGCACGCCCTCCCGCGCCAACCACCGGCACAGGCCCGCCACCAGGACGCTCTTGCCCGCGTCCGACGTGGTCCCGGCCACCAGCACCGCACCACTCACAGCCGCACCCCTCCACCGGCGCCCGAGGGCTGCCATCATCCTCGTCATGGTCCACACGCCCGCCACCGCGGTCCTGCTGCACAGCCCGTTCCTGGGACCCGCCAGCCTCGCCCCGCTCGCCGACGCGCTCGCCGCGCTCGGCAGGCCGGTGCTGCCGCTGGACGTGCGGGTGACGGTCAACGCCGCACCCGTGCACCAGCGGATCATCGGCGTGCTCACCGACGCGGTCGAGGACTCGGGGGTGAGCGGCGACCTGGTCCTGGTGGGGCACAGCGGCGCCGGTCCCCTGCTCCCCGCGTTCGCCGAGGCCCTCGAGGAAGCCCCCGTCACCGGTCTGGTCTACCTCGACTCCGACCTGCCCACGCCCGGCCGGAGCTGGCGCGACACCGCGCCCGCCGAGCTGTTCTCCGCGCTGAAGGCCGCCTCGCGCGGCGGGCTGCTCCAGCGCTGGGACCGCTGGTTCGGGCCGGACGAGATCGCGGGTCTGGTGTCCGACGCGGACCTGCTGGCCGAGATCACCGCCGAGGCCCCCGAGGTGCCGCTGGCGTTCCTCAAGGAGCCGCACCCGACGATCGAGTGGACCGGCCCGCAGGCGGTGCTGCGGCTGAGCCCCGCCTACGACGAGGCGTGCGCCCAGGCCGCCGCGCTGGGCTGGCCGGTCCGCGAGCTGGACCTGCACCACCTGGCCGCCGCCACCGACCCGGAGCCGGTGGCGCTGGCGCTGGCGGACCTGCTGGACCGGTTGGGCCGCTGATCGCCCGGTCGGGCCGAGCGCGGCGGCCCGACCGGGGTCCGGGCTCAGCAGGTGGTGAGGATCTCCGCACCCTCGTCGGTGACGACGAGGGTGTGCTCGAACTGCGCCGTCCAGCTCTTGTCCTTGGTGGTGACGGTCCAGCCGTCGTCCCACATCTCGCCGTCCGCGCCGCCGAGGGTGATCATCGGCTCGATCGTGAACGTCATGCCGGTCTCGATGACGGTGGGCACGTGCGGCGCGTCGTAGTGCAGCACGATCAGGCCGTTGTGGAACGTGCGGCCGATGCCGTGGCCGGTGAAGTCGCGCACCACGCCGTAGCCGAAGCGGTTGGCGTAGGCCTCGATGACGCGGCCGACCACGTTGAGCTGGCGACCGGGCTTGACGGCCTTGATCGCGCGCATGGTGGCCTCGTGGGTGCGCTCGACCAGCAGCCGCACCTCCTCGGACGCCTCGCCCGCGATGAAGGTGGCGTTGGTGTCGCCGTGCACTCCCCCGATGTACGCGGTGACGTCGATGTTGACGATGTCGCCGTCCTCGACCACGGTCGAGTCGGGGATGCCGTGGCAGATGACCTCGTTGAGCGAGGTGCAGCAGGACTTCGGGAAGCCCCGGTAGCCGAGCGTCGACGGGTACGCGCCGTGGTCGCACAGGAACTCGTGGGCGATCGCGTCGAGCCGGTCGGTGGTGACGCCGGGCACGACGGCCTTGCCCGCCTCCTGCAGCGCCTGGGCGGCGAGCCTGCCCGCGACGCGCATGGCCTCGATCACCTCGGGCGTCTGCGCCCACGGGTCGGTGTTGCGCTGCGGGGCGGGGCGGTCGACGTACTCAGGCCGCTCGATGTGCTCGGGGACGGGGCGCCTGGGGGACTGCGTCCCAGGCTTCAGGACGGCGCGCACGGACATGCCCCAACACTACGACGCCCGCCGGAGCGCCAGCAGGGGAGTCCGGGGTCAGCCGACGGCCCGCAGGAACCTGCCCGTGGCGTCCACGGCGGGCGTGGAGGCGTTGGCCCCCAGCAGGAGCGTGGCGAACGCGACGTCGCCCCGGTAGCCGACGAACCAGCCGTGCGAGTTGACCCCGTCGCCGTACTGGGCGGTGCCGGTCTTGCCGCGCACGTCGCCGAGGCCGCGCAACTGGGTCGCGGTGCCCGACTCGACCACCTCGCGCATCATCGCCCGCAGCGGCTCCAGGACGGCGGTGGACGGCGCGGGCGGCTGCCGGTCGGCCTTGGTGGCCTGCTCGCGCATCAGGGTCGGCGTGGGCATCGTGCCGCCCGCGGCGGTCGCGGCGACCAGGGCCATGCCGAACGGGCTGGCGACCACCTTGCCCTGCCCGAACCCGTCCTCGGCCCGCTCGACCACGTCGGCGGCCTCGGGCGCGGAGCCGGTGATGGTGGTGACGGCCGGGATCTCGAAGTCGACGCCGAGGCCGAACGAGGCGGCCTGCTCGGTGAGCGCGGCGGGGGGCAGCTCGGCGGCGAGCTGGGCGAAGGTGGTGTTGCAGGAGAACGCGAACGCCGACCGCAGCGGGATCGTGCCCTTGTCGAACTCCTTGTCGTTGGGCACGATCCGGCGGCCGTCGACGGTGGTCCTGCCGGGGCAGGGCAGCGGGCTGTCCGCGCTCGCCCTGCCCGCCGCCATGGCCGCCGCCGCCGTGACGATCTTGAACGTGGAGCCGGGCGGGAACTGGCCGGTGAGCGCGATCGCGCCCTGCTCGTCGGCGGGGCCGTTCTGCGCCACGGCCAGCACCTCGCCGGTGCCGACCTGGAGCGCCACCAGCATCGCGGGCTGCGCGACCGGCTCCAGCGCGTCCTCGGCGGCGTCCTGCACCCGGCGGCTGAGCGTGGTGGGCACGGCGTGCGCGGGCTCGGGCTGCTGGTCGAACAGCGTCTCGACCTCCTGCCCGGAGGAGTTGGCGGTGTAGACGCGGAACCCGGCCTCGCCCGCGACGGTGTCCTCGACGGACTTGCGGATCGCGGGCAGCACCTGCGAGCCGTAGTCGCGGGACGGGGCCAGCAGGCTCACCTGGCTGGTGAAGCGGACGCCGGGCAGCTCGTAGATGGCGGGCTTGACCGACTGGTAGTCGGCGTCGCGCAGCGCGGCCACCAGGTACGACTGGCCCTCCGGGACGGCGGCGGCGCCGTCGGCGACGGTCTTCGCGGTGATCTTCCCGTCGAACCGGGACAGCGCGGCGGCCAGCGAGTTCGCGACCGCGTTCACGTCCCCGGCCTCCTTCGGGCTCAGCAGCACCGAGACCACCGTTTCGGGTGACATCAGCGCGGTGCCGTCCCGGTCGAGCACGGGGGCGAGCGCGGGCTTGACCTCGGTGAACCCGAGCGACTGCTGGGCGCCGAGCTTGGGGTGCACGACCGAGGGCGCCCAGTGCACCTTCCAGTCGTCGGCCTCGCGGCGCAGCTCCAGGGAGGTCTGGTACTTCCACCGGTGCTCGTTGGGCAGCTGCCACTCCAGGGTGGCGTCGGCGGGGGCGGTGGCCCCGCTCTGGTCGCCGACCCGGTCCACGGAGGTGGTCAGCCCGGTGGGCCTCAGCGCCCCGCGCACCTTGTCCAGCAGGTCCTCGGCGGACGTCGGGTCGTCGGTGAGCCTCGCGGCGCCCTCGGTGTCGCCGGAGGCCACCTTGGACAGGAAGTCGCCGAGCGCGTCGCCCGGCCCCGGCTTGGACGTGAAGAGCCCGCACCCGGAGAGCAGCAGCAGGAGGCACACCGGACCGGCCAGCTTGGGCAGCAGCACCACCGCAGTATGCCCCCGGATCAGAAGAGCACGGTCGCGTACTGGCCCACCTGCGTGAAGCCGATCTTGCGGTACGCGGCGCGGGCGGGGCTGTTGTAGCCGTTGACGTACAGGCTCGCGGTGCGCCCGAGGCCCCGGACGAGCCGGTCGGCGACGGCCGCCGTGCCCGCCGCGCCGACGCCGTGCCCGCGCCGGTCCGGCCGCACCCACACGCCCTGGATCTGGCCGACCTGCCGGGACATGGCCCCGATCTCGGCCTTGAACACGACCTCGCCGTTCTCGAACCGGGCGAACGCCCGCCCCGACGCGATCAGCTCGGCCACCCGCGCCCGGTAGCCCGCGCCGCCGTCCTCGGCGCACGGGTCGACGCCGACCTCCTCCACGAACATGGCGATCGCGGCGGGCAGGTAGCGCTCCAGCTCGGCGGGCCGCACCGGCCGCACCAGCGGGTCGGGGCGCACCGACGGCGCGCCGCCCATGGCGAGCAACGGCTGGTCGGCGCGCACCTCGCGGGCCGGGCCCCAGTCGCGCTCCAGCTCCTCCCACAGGCCGATGACCTGCTCGGCGGGGCCGACCAGCGAGGAGCACGTGCGGCCCCGCCGCCGGGCCCGGTCGGCGAAGCCGCGCAGCGCGGCCTGGCCGCCGGACAGCGGGATCAGGTTCGGACCGGCGAAGCACAGCGCGTCCACGCGCCCGCCGCGCAGCGACCGGTGGTCGAACGACCAGACCTCACCGCCCAGCCGCCACGGGTCCAGTCCCACGGACTCCACCCGCGCGGCGACCATGCAGGACGCCACCGGGTCGGCGGCGAGCGCCGCCAGCACCCCGGTGAGCTCCCGGTCGTCGAGCACCCTCGCTCCGGCAAGCCTCAGCACACGGCCAAGCCTGCCAGAGAACGCGCCGGAGCGGGGTGCCCGCCACCCGCTCAGCCGACCGTGACGACGGGCTCGCCCGAGCCCTCGTTCTCGCCGACCTCCTCGGCGATGCGCATGGCCTCTTCGATCAGGGTCTCCACGATCAGGTGCTCGGGCACGGTCTTGATGACCTTGCCCTTGACGAAGATCTGGCCCTTGCCGTTGCCGGAGGCCACGCCGAGGTCGGCCTCGCGGGCCTCGCCGGGGCCGTTGACGACGCAGCCCATGACGGCGACGCGCAGCGGCACCTCCATGCCCTCCAGACCGGCGGTGACCTGCTCGGCGAGGGTGTAGACGTCCACCTGGGCCCGACCGCAGGACGGGCAGGACACGATCTCCAGCTTGCGGGGCCGCAGGTTCAGCGACTGCAGGATCTGGTTGCCGACCTTGACCTCCTCCACCGGCGGGGCCGACAGGGACACCCGGATCGTGTCGCCGATGCCCTGGCGCAGCAGCGCGCCGAAGGCCACGGCGGACTTGATCGTGCCCTGGAACGCCGGACCGGCCTCGGTGACGCCCAGGTGCAGCGGGTAGTCGCACTGCTCGGCGAGGATCTCGTAGGCGCGCACCATGACCACGGGGTCGTTGTGCTTGACGGAGATCTTCAGGTCGTGGAAGTCGTGCTCGGCGAAGAGCGAGGCCTCCCACAGGGCCGACTCGGCGAGGGCCTCGGGGGTGGCCTTGCCGTGCTTGGCCATCAGGCGCGGGTCGAGCGAACCCGCGTTGACGCCGATGCGGATGGGGGTGTTGTGGTCGCGGGCCGCCGCGGCGATCTCCTTGACCTTGTCGTCGAACTTCTTGATGTTGCCGGGGTTGACCCGGACCGCCGCGCAGCCCGCCTCGATGGCGGCGAACACGTACTTCGGCTGGAAGTGGATGTCCGCGATCACCGGGATCTGGGACTTCTTCGCGATGGCCGCGAGCGCGTCGGCGTCGTCCTGCGAGGGGCAGGCGACCCGGACGATGTCGCAACCGGACGCGGTCAGCTCCGCGATCTGCTGGAGGGTGCCGTTGATGTCGGCGGTGACCGTCGTGGTCATGGACTGCACCGACACCGGGGACTCGCTGCCGACGCCGACCGACCCGACCTTGAGCTGGCGGGTCTTGCGCCGCTCGGACAGGACGGGAGGCGGCAGCGCAGGCATACCGAGCATGACGCCGTCAGTCATGGGACAAGCACCTTTCGGGGAGGCACATCAGGGGAGCCGGATGGGGTTGACGATGTCCGCGGTGATCGTCAGCAGCGTGATCGCGCCGCCGACGAAGATGGCGAAGTAGGTCAGCGGCAGCAGCCGCAGGTAGTTCACCGGGGGACCCGCGGGCTTGCCGCGCAGCTTGCGGACCCAGTCCCGCACCCGCTCGTACAGGTTGACGGCGATGTGGCCGCCGTCCAGCGGGAGCAGCGGCAGGAGGTTGAACACACCGATGAAGAAGTTCAGGCCCGCCAGCATGAGCCAGAAGAAGTGCCACAGGCCCGCGCTCACGGCGTCGCCGCCGAGGATGGAGGCGCCGACCACGCTGACCGGGGCCTCCGGGTCGCGCTCGCCGCCGCCGATGGCCTTGATGACCATGGGGATCTTCTCGGGGAACTTCATCAGGCCGCGCCAGGTGTTGGCGAACATGTCGCCGGTGTACTTCGTCGCGCCGCCGAACGCGGTGAGCGCGTTGTACTCGTACAGCCTGGACTTGGCGACGCCGATGACGCCGACGGTGTCGACGTAGGTGGAGCCGTCGGCGCGCCGCAGCTCGCGCTCGACCCGCGGGATGTCGATGGTGAGGGTGACCTCGTCGTCACCGCGCAGGACGACCACCTCGGTGGGGCCGCTGCTCTGCTGGATCTTCTTCTGGACCTCGATCCAGGTCGGCAGGCGCTGGCCGCCGACCGCGAGGATCCGGTCGCCCTGCTGCACGCCCGCGCTGACGCCCGGCGTCGGGTCGGTCGGCGCGCAGGTCGGGTTCTCCTTCTTGGCCTCGGCGGCGGTGGCGGGCACGCACTGCGAGACCTTCGACACCACGGCCTCGTCCCGGATGTCCGGGAGGCCGATCGTGGCGGCCATCGCGTACAGCACGACGAAGCCGACGATGAAGTGCGTGATGGACCCGGCGGAGAGCACGACGACGCGCTTCCAGGTCTTCTGCCGGTAGAAGGCGCGCTTCTCGTCCTCGGGCGGCAGCTCGTCGAGCGCGGTCATGCCGACGATCTCGCAGAAGCCGCCCGCCGGGATGGCCTTGAGGCCGTACTCGGTCTCGCCCTTGCGCGTCGACCAGATGCGCGGGCCGAAGCCGATGTAGTACCGGGTCACCTTCATGCCGAAGGCCTTGGCCGTTGCCAGGTGTCCCAGCTCGTGCAGCGCGATCGAAATGCCGATGAGCAGCGCGAACAGCACCACACCCAACACGAACGCCAC

Protein sequences of DBSCAN-SWA_2

>NZ_CP023445|6738135:6789691|6786389_6787241_-|WP_096498054.1|DBSCAN-SWA
MRLAGARVLDDRELTGVLAALAADPVASCMVAARVESVGLDPWRLGGEVWSFDHRSLRGGRVDALCFAGPNLIPLSGGQAALRGFADRARRRGRTCSSLVGPAEQVIGLWEELERDWGPAREVRADQPLLAMGGAPSVRPDPLVRPVRPAELERYLPAAIAMFVEEVGVDPCAEDGGAGYRARVAELIASGRAFARFENGEVVFKAEIGAMSRQVGQIQGVWVRPDRRGHGVGAAGTAAVADRLVRGLGRTASLYVNGYNSPARAAYRKIGFTQVGQYATVLF
>NZ_CP023445|6738135:6789691|6767868_6768501_+|WP_096498051.1|DBSCAN-SWA
MADHPRVVLLKPLVDAPNIEVGDYTYYDDPERATEFQTRNVLYSYGPERLVIGKYCALGTGTTFIMAGANHLTRGPSTFPFTIFGGAWAEKTADIMAAAPSKGDTVVGNDVWFGCGATVMPGVTIGDGAIIATGAVVTSDVAPYTVVGGNPAQAVRQRYPDDKIELLLRAAWWDWPVELVTEHVREIMAGKVKQLAEIAEENGLLGPKPR
>NZ_CP023445|6738135:6789691|6782914_6783622_+|WP_096496562.1|DBSCAN-SWA
MVHTPATAVLLHSPFLGPASLAPLADALAALGRPVLPLDVRVTVNAAPVHQRIIGVLTDAVEDSGVSGDLVLVGHSGAGPLLPAFAEALEEAPVTGLVYLDSDLPTPGRSWRDTAPAELFSALKAASRGGLLQRWDRWFGPDEIAGLVSDADLLAEITAEAPEVPLAFLKEPHPTIEWTGPQAVLRLSPAYDEACAQAAALGWPVRELDLHHLAAATDPEPVALALADLLDRLGR
>NZ_CP023445|6738135:6789691|6766939_6767839_+|WP_096498050.1|DBSCAN-SWA
MPLGSEASAALVRRRADGAAERGAVLYVHGFADYFFQRHVAEHFAALGYDFYALDLRAYGRSLRPGEVANHVEDLSTHFEELDAAVRVVREEDGHRGLVVVGHSTGGLTTSLWAHERRLDGALDALVLNSPWLDLAEPWVVRTVGTAVVRGVGRLAPKLVLKPGLGPVYGQSIHRDHHGEWEFDTAWKPIEAFPVTAGWLRAVRVGHARLHRGLDVRVPVLVLHSARSHLKARRWSAEAMTADAVLDVGHMRRWAPRIGRDVSLVQVEGGMHDLFLSAAPVRERALAEVDAFLERKVER
>NZ_CP023445|6738135:6789691|6771094_6771895_+|WP_096496555.1|DBSCAN-SWA
MEQASWVPASVDLDRPSTARMYDYYLGGSHNFAVDREAAKAVEHVFPGMSGAARSLRTFLRRSVRYLLDQGIDQFLDLGSGIPTVGNVHEIAQAANPAARVVYVDIEPVAVAHSTAILSANPLATAIQADLRDPASVLENEDVRRLLDFDRPIGVLMVAVLHFVPDADDPHGAIARYRDALVPGSFLAISHATVEGVQVDAEQDTARVQDVYKRTESPLIFRDRAEVTKLFDGFEVVEPGVVPLSEWRRDSDDAYTSAYVGVGRKV
>NZ_CP023445|6738135:6789691|6762507_6763257_-|WP_096496550.1|protease|DBSCAN-SWA
MRISSRLVAALALVAVQLASQLVAAPAALAVVGGSVAGRAPWVAALLDARGSHFCGGALIAPDRVVTAAHCTQERGLLGPRDRAPRQLTVVLDRHDLRTRGGVRVGVSGIWRHPAFTDVGRGDDLAVLQLDGPVAFEPVRVGDAVAGRTATAYGWGRTAESGPVSSVLRQVDVPIRADHDCAAALAGYRADAMLCAGFPDGGRDACTGDSGGPLVSDGLLVGVVSYGRGCARAGQPGAYTRLGHYRDRL
>NZ_CP023445|6738135:6789691|6787294_6788452_-|WP_096496565.1|DBSCAN-SWA
MTDGVMLGMPALPPPVLSERRKTRQLKVGSVGVGSESPVSVQSMTTTVTADINGTLQQIAELTASGCDIVRVACPSQDDADALAAIAKKSQIPVIADIHFQPKYVFAAIEAGCAAVRVNPGNIKKFDDKVKEIAAAARDHNTPIRIGVNAGSLDPRLMAKHGKATPEALAESALWEASLFAEHDFHDLKISVKHNDPVVMVRAYEILAEQCDYPLHLGVTEAGPAFQGTIKSAVAFGALLRQGIGDTIRVSLSAPPVEEVKVGNQILQSLNLRPRKLEIVSCPSCGRAQVDVYTLAEQVTAGLEGMEVPLRVAVMGCVVNGPGEAREADLGVASGNGKGQIFVKGKVIKTVPEHLIVETLIEEAMRIAEEVGENEGSGEPVVTVG
>NZ_CP023445|6738135:6789691|6783666_6784524_-|WP_096496563.1|DBSCAN-SWA
MSVRAVLKPGTQSPRRPVPEHIERPEYVDRPAPQRNTDPWAQTPEVIEAMRVAGRLAAQALQEAGKAVVPGVTTDRLDAIAHEFLCDHGAYPSTLGYRGFPKSCCTSLNEVICHGIPDSTVVEDGDIVNIDVTAYIGGVHGDTNATFIAGEASEEVRLLVERTHEATMRAIKAVKPGRQLNVVGRVIEAYANRFGYGVVRDFTGHGIGRTFHNGLIVLHYDAPHVPTVIETGMTFTIEPMITLGGADGEMWDDGWTVTTKDKSWTAQFEHTLVVTDEGAEILTTC
>NZ_CP023445|6738135:6789691|6777019_6778378_-|WP_096496559.1|DBSCAN-SWA
MSVHIATDPGDDATVGTHPVTGAADQTTADPTTAAPATAPPAEPAPAPRPNRGAALVGSTLLAVGVALAAANLRPAVTSLASVLGDVRASLGATTAWTSLLTAVPTVCFGVAAFAAPWLGRRFGMARAVGASLVVLTLGLVLRVLDGPAVLLGGTFTACAGIAVCNVLIPVVVKESFPDKVGFLTGVYTAALAAGAAVGAALTPTLETALGSWQLAAATWALLSTAALLVWSASARHGAAPAVAVPAASGAAPARGAHPVQQRRTSVLRSPLAWVITVFFGLQSLLAYTVMGWLPQIMADSGVDRTTAGMLLAITMVLGVPVSLVVPPLATRWGSQSWLVVLLGSLSIAGILGLAIAPVAAPGLWVVLIGTGMCVFPLALVIISLRTATAADTAKLSAMAQSIGYLISAAGPFAFGVLRDVTGAWTVSMYVLAGILVALIALGVIAGRPRTI
>NZ_CP023445|6738135:6789691|6758919_6759813_-|WP_096496546.1|DBSCAN-SWA
MTTFSASDLPDLTGRTAVVTGANSGIGRVTARVLAARGARVVLAVRSPAKGREAASTMPGSTEVRELDLADLASVRAFADGFGDPVDLLINNAGLMTPPLSRTADGFESQFGTNHLGHFALTNLLLPRITGRVVTVSSGAHRVGKIDFADLNWERKPYRAMAAYGQSKLANLLFSAELQRRLTAVGSPVLATSAHPGLAATNLFRAQGGDNPLNRLVNAGVRAVGQTDEGGAQATLHAALATVPGNAFSGPSGALGKGAPKLVGRSRAAQDAELARRLWTVSEELTGVTFPLPLTSA
>NZ_CP023445|6738135:6789691|6749890_6750676_-|WP_096496539.1|protease|DBSCAN-SWA
MAKTLRRLAKFIGLGVAAAAIGLMTTPVSSASDVTPFIVGGARASISEAPWAVYLASSSGSQFCGGTLVKANKVVTAAHCVAGRSASSTRVVIGREDKQSTAGTVATVSSIWSHPSYRTATSGYDVAVLTLGTSVSGTYLPLATPSDTALYAAGTNAVAYGWGATCSGCSTSRYLLKVTVPVTSDATCKTAYSQYSNTSMVCAGVPAGGKDTCQGDSGGPLVAGGKLIGATSWGNGCALPNYPGVYARVAAYYSVLSAQIG
>NZ_CP023445|6738135:6789691|6780321_6781215_+|WP_096496561.1|DBSCAN-SWA
MKPAHSAVAVLVAVIWGVNFVVIKVGLAEFPPLLFSALRFLLAAVPAVLFLGGPRVAWRWVFGVGLALGVVKFGLVFTGMHAGMPAGLSSLVLQSQVVFTVVLSAVVLGERPRPAQVLGLAVATTGFVAIALDYRVSSPVSALLLVVGGALAWGVANVLTRKAQPPDSLRFIVWVSAVAVLPLLALSLLVEGPEADLAALRGADWAGVGSLLFVAWGSTLLGFALWGFLLRTYPAPRVVPFALLVPVAGMLSGWLLLDEEVTAVRLGAAALVVAGMGVATLTRPRRRAEPVVAAVPV
>NZ_CP023445|6738135:6789691|6775005_6775533_+|WP_096496557.1|DBSCAN-SWA
MSLDRPVAPDPYSLLPTAPAFQVTSTDVADGQPLPQAQVFEGGNTSPQLSWSGFPEGTKSFVVTCFDPDAPTPSGFWHWVAVNLPVSTTSLDTGAGADDDSLPGGAFHVRSDYGTRAFGGAAPPKGDRPHRYFFVVHAVDVEALDVDGDASPAAVSFNLAFHTLARAIITPTYQH
>NZ_CP023445|6738135:6789691|6768559_6770923_-|WP_096496554.1|DBSCAN-SWA
MGDTLALPVLPLDDTVVLPGMVVPVRLTGSDAGAEARAAVEAATSAAGGVNGARVLLVPRLDGRYAKVGALATVEQVGRLAGGERAAVLRATERVRIGTGTTGPGAALWVEATVVEEPPPDERAHSLARDYRAVVTTILQQRGAWQVVDSVRQVDGPSALADLAGYAPYLENDQKVWLLETGDVGDRLERLLEWGRAHLAELDVAETIAKDVKEGVEKQQREFLLRQQLAAIRKELAELDGKPATEEQDYRARVEAAELPEKVREAALREVDKLERTSEQSPEVGWIRTWLDTVLDLPWGERTEDSYDIAGARAVLDADHAGLDDVKERITEYLAVRRRRADRGMGLVGGRGGGAVLALVGPPGVGKTSLGESVARAMGRKFVRVALGGVRDEAEIRGHRRTYVGALPGRIARAISEAGSMNPVVLLDEIDKVGADHRGDPTAALLEVLDPAQNHTFRDHYLEVELDLSDVVFLATANVLESIPGPLLDRMELVRLDGYTEDEKVTIARDHLLPRQVERAGLEPGDVEVTGAALRRLAGEYTREAGVRQLERSLARVLRKVTAGVALDRAELPVTVDGGDLEGYLKSPKFTPESAERTAVPGVATGLAVTGAGGDVLFVEAALAEPGTGASGVVLTGQLGEVMKESAQIALSYLRAHDERAATLDGRGVHVHVPAGAVPKDGPSAGVTMVSALASLLSGRPVRSDVAMTGEVSLTGRVLPIGGVKQKLLAAHRAGITTVLLPARNGPDLEEVPQDVRDALTVHLVGDVREVLALALEPEAAAATTAA
>NZ_CP023445|6738135:6789691|6771969_6773904_-|WP_096498052.1|DBSCAN-SWA
MAAGDDGDDEDFDRCCDLTMRGGATSGIVYPLAVVELSKHYRFRSLGGASAGAIGASFAAAAERGRDSGGFDRLADTVSWFAAGQQRLAQLFQPTRATRKLYRLVTATMQSRETTGRSAAVSLVFALLGAIGLRAKAALAAALLVWLAGPVLWFGAVAWPGFPTWGLAAIVVVAVLAVPWVAAKALPSGRGPLPARIGLLLLAAVPLYPIVPRLRADWAVLASAATAGVVWLVLGFGLASAVVLIYAGGVRRFVRERAASIGFGLVPGTGGYRSSWWDRRCGMPKSTGVPPLSDWLADSLDHLAGVRGLRFSDLTTNLVLMSTDVSEGRPCRLPFTSDDRWLFCADCLAAVLPARVVDLLGDEGADDARCPLHPATALRVLPADLPVALAVRMSTPMPGLISAVPLVRADPEPRVHWFSDGGITSNFPIHFFDTLLPRWPTFGLTLQGYPAPDAPDVWLPEQDASQEGRPWRAVTGAVGFAQAVLDTALGWRDAMQSALPGFRGRIAHVRLRGGEGGTNLFMRPETIRALAERGRVAGELLRTRFTQEGGERTARYRWIRMRIAMREYQELARQARERGEQYRELADGYPVPEELKSWFADPPAGTDPFAADVRLTLDQLGGLVPGPFDGAPPVNPDLRLNPAE
>NZ_CP023445|6738135:6789691|6750764_6752024_-|WP_096496540.1|DBSCAN-SWA
MIGLFASTERGRAQAKELAAFLGPDAVVPDGPVAPALRRMWPVLGSAVFFEGSETVVRLVAPLLRDERSDPGVVCVDGAFAIALLGGADALAQRVADVLGRTAVTTAPPTASPLDELLELLDATAEGDAAACGEAMRAGEPVALANPLGFPLPALPDNVLPAGHEAAWTVLLDDRVPRTELGDHVVRVIPRTLVIGIGASAGVTSTDVSGALAKLAADGRLDLRAVRAFATLDRKTEEPGIVDAVEDWGFWHGSTTTPLLGYPGEELAVIPVPNPVELAIGIPSVAEAAALRGAAELSAGGRVEIAAEKVKGARATVAAARVLPRGRLALIGLGPGGADDRTPRAEAELRRASVVVGPPECVDQVRHLLRPGTSVRADGAVRLAEQGVAVALVAPDAGPVVAGPVHADVVRVTGVTGQL
>NZ_CP023445|6738135:6789691|6760827_6762006_+|WP_096496548.1|DBSCAN-SWA
MTEHTGESVFDWIDARAEARAEAGLTRRVRPRPASGGALDLAGNDYLGLARDKRVVGAAAAASMRWGAGSTGSRLVTGSTELHTELEYELANFCGAQAALVFSSGYAANLGALTALSGPGTAIVADQHIHASLIDGCKLSRADVVVAGHRDLPQVTRALSTRGERRGLVVTDSVFSVDGDTAPLAELAAACRRHGAGLVVDDAHGLGVVGDGGRGAVHAAGLAKSPDVVTTVTLSKALGAQGGAVLGPGRVIRHLVDTARTFIFDTGLAPGSAAAALASLKALKEEPERPERVREAARLLSERLRERGFRASEPSAAVVSVLAPSPEVAVAWAEACRERGVLVGCFRPPSVPDQVSRLRLTARADLSEADLARAVEVIAEAGASAGAGSRPR
>NZ_CP023445|6738135:6789691|6753208_6754339_-|WP_096496542.1|DBSCAN-SWA
MTGRVAFVGAGPGAADLITLRGARRLAEADVVVWAPSVVEAECVREHARPGAELVDFSRVTESEVVEVYRRAAASGQAVVRLHAGDPATWGGLREQHDACLRLGLEIEVVPGVTQVSAAAASVGRELTTSEVAQSLVLASPESAEHVRELAAHGTTLALSASAARADRVAEQLRAGGYADTTPVVIAYKVSLPDAVLVRTTLGELESAVKEHKLYRSTLFLVGDALRAPVRRGAPIGDEPVRQPRASKWRTARATGAESRSEAAWSAVHDLQETARSRWARAREESGADGAELPIARSLAEPAEPAGSVEPTAAGPVAEEPAVDSLPGQAGSPEEAPEPRRKPPVAAARKRTVSVQASTTPRKPAPARGKKSKRTG
>NZ_CP023445|6738135:6789691|6779332_6780247_-|WP_096496560.1|DBSCAN-SWA
MLDLGRLRALHAVARHGSVGAAASALGYTPSAVSQQITKLERETRAVLLERRGRGVVLTDAALLLADTAERVLALVEGVEVALERQRGQVVGELRIGAFSTAARGLLPPALAELAVRHPELDARLVEQDPPEAIGAVARGELDLAVAHDWVNAPLPVHESLARVRLGEDYADVLLPSAHRLAGRAAVGVADLAGERWICQPEGTICHDWLVNAFRAEGVEPLLAHRVGEYETQLALLERGVGVALLPRLGRGALPEGVRAVPFEPRPTRRVFVVWRAQAARRPAIGAVAQVLREVWEAWVPTRG
>NZ_CP023445|6738135:6789691|6778461_6779133_+|WP_015804574.1|DBSCAN-SWA
MPLATTRRAGLVDQVIDQMRGAIASGEWPVGRRIPPEPELVTALGVGRNTVREAVRALAHAGLLEVRQGDGTFVRATSELSGAVRRLCGSELRDVLQVRRTLEVEGARLAATQRTEEELARLEVALAERDSALAAKDWERLVERDAQFHELLLQCSHNTLLAELYQGLTEAVRASIDATVRTAPDDDDLSHEGLLQAIRDADPARAALEAGGFLEELLERHGE
>NZ_CP023445|6738135:6789691|6775574_6776954_+|WP_096496558.1|DBSCAN-SWA
MRHFDLVVIGTGSGNSIVDEAFAAWDVAIVEKGVFGGTCLNVGCIPTKMFVHTADLAAGPASAARFGVDASLDGVRWTDVRDRIFGRIDPIAEGGRRWRESGSANTTVYSGTARFTGPKTLDTGAGETITADRFVIAAGSRPVVPDVPGLVETGFHTSDTVMRLDRLPRRMVILGSGFVATEFAHVFSSFGVEVTLVARSGALLRAEDDAVSARFTELASAKWDVRLDRRAVRAERVDGVARLHLEGPDGPEVVEAEELLVAVGRQPNADLLDVAATGVALNDKGRVAVDEFQRTSVEGIYALGDISSDYQLKHVANHEAKVVRHNLLNPDAPIASDHRFVPSAVFSSPQIASVGLTERDAVAKGVSYVSVEQPYASIAYGWAMEDTTGFVKLLADPVTGQLLGAHVIGPQAPTVVQPLIQAMSFGLDARSMAKGQYWIHPGMPEVVENALLALPLKDA
>NZ_CP023445|6738135:6789691|6755903_6756518_-|WP_096496544.1|DBSCAN-SWA
MPQGQPTAVPSDGLTTRQRRNRPLLLVHTGPMKGKSTAAFGLALRGWNQGWDIGVFQFVKSAKWKVGEEAAFRALGELHESTGQGGPVQWHKMGEGWSWSRKAGTEEDHAAAALEGWREIARRIADERHGLYVLDEFTYPLKWGWIDVDEVVEVLVNRPGHQHVVITGRDAPRALVDAADLVVEMTKVKHPMDAGQKGQRGIEW
>NZ_CP023445|6738135:6789691|6746551_6748057_+|WP_096496537.1|DBSCAN-SWA
MPPVSQSRSERPQSSRRPRRRSGQGNRRPQHVDAPLASTVPDHVESTLPEGPLPSFSELGLADELVRALATAGITEPFPIQAATLPDSLAGRDLLGRGQTGSGKTLAFGLALLSRLAGGRAKPHMPRALVLVPTRELAMQVEEALSPFARALGLWCRTVVGGTSFPRQIDALRRGVDLLIATPGRLSDHVRQGTADLSEVMFTALDEADQMADMGFMPQVRAILDLTPENGQRLLFSATLDGDVDKLVRQYLHDPVVHSVAPPTGSVTTMEHHLLFVSAEDKQSVVTEVAAREGRTIMFVRTKHHVDRLAKKLRSMGVHAGALHGGKAQSARTRVLGQFREGTTPVLIATDVAARGIHVDDVSLVVHVDPPADPKDYLHRAGRTARAGQSGTVVTLVTHDQRRAVQGLTSRAGIRPESTKVRPGDDELIRITGAREPSGVPVVEPEVQPRGRRGGAGGGAGARRGGGGFFRGGREGGRGEGGGRDRDRSGGRPRRSAAPQH
>NZ_CP023445|6738135:6789691|6765794_6766829_-|WP_096496553.1|protease|DBSCAN-SWA
MSEEIERSTSRVRFPGISPRAYEHPVDRGALAVLRAVPGIGPVLKSVAGAFTERGERLGYLATSIRVGPKQYPALDRLRNETAATLDLDPVPELFITRNPQPNAMALGIDKPFIVLTTGLVDLLDHDGLRFAIGHEMGHVLSGHALYQTILMRLMQLQHSLGWMPAGYWAVRAVIAALHEWYRKTELSCDRAGLLCAQDPAAALRVHVALAGGMDLTQVDTAEFLKQAKEYEQVEDVRDSVLKLIRTWPLTHPMAVVRAAELQRWAASEEYRAILSGDYRRREDDHASSTFTEDLKEAARSYKSDAAESEDPLMKVVNDLGGVVADAAGKVRGRFSGFGSPSGN
>NZ_CP023445|6738135:6789691|6740693_6741461_+|WP_096496535.1|DBSCAN-SWA
MLVLLPPSETKATGGSGAPLDLDALSHRELNPVRDKLVTALVDLAADVPASLAALGLSERQAGEVGRNAELRTSATTPALRRYTGVLYDALDVPSLTKAERDRAFARIGVVSALFGLVGGGDAIPAYRLSGGSALPATGPLGALWRPALTPVLAEADEFVVDLRSGPYASLAKAPAAVVVRVVSDDGSGRRKAVSHFNKAHKGLLARALVRSRTEPSTVAGLVKVAASAGLTLEETGAKALDLVIIGNPADKPAA
>NZ_CP023445|6738135:6789691|6738135_6739881_-|WP_096496534.1|tRNA|DBSCAN-SWA
MITRMSSLFLRTLREDPADAEVPSHKLLVRAGYVRRVAPGGYSWLPLGLRVLRNIERVVREEMDAIGAQEIQFPALLPKEPYEATNRWTEYGPNIFRLKDRKGADYLLGPTHEELFALTVKGEYSSYKDYPVALYQIQTKYRDEARPRAGILRGREFVMKDSYSFDLTDEGLAEAYQRHRAAYIKIFDRLGMDYVIVSATSGAMGGSASEEFLAVAPNGEDTFVRSTESDYAANVEAVTTPAPPAQPVEGRPEAQVHSTPATPTIDTLVEFFNNAGLGREFTAADTLKNVLVKTRVPGSDWELLAIGLPGDREVDLKRLEAAVEPAEVAMLDEADFKAHPFLVKGYIGPGALLANKVRYLVDPRVVEGTAWVTGADRHEHHVVDLLCGRDFTPDGTIDVAEVREGDPSPDGKGVLVAARGIEIGHIFQLGRKYADAFSLDALGPDGKPVRITMGSYGIGVSRLVAAIAEQSHDDRGLIWPRNVAPADVHVVVAGKDATLLEGGEKLAGELSSAGLSVLLDDRKASPGVKFADAELVGVPTILVVGRGLAGGLVEVKDRRSGERVEVPVDEAVQHVLAVARG
>NZ_CP023445|6738135:6789691|6748364_6749582_-|WP_096496538.1|DBSCAN-SWA
MHGEQHYLVGLDLAGKRVVVVGGGSVAQRRLPRLVSSGARVELVSPEVTPTVQGVVDSGAVTWHARRYADGDLDGAWYVLACTSDPEVNARITADAEARRVFCVRADVGALGTAVTPASGNHDGLLVGVLASGDHNRSARVRDGVLSALRDGTLADQHDQPAGVALVGGGPGDPDLITVRGRRLLARADVVVADRLGPVWLLDELPPHVEVVDAAKIPYGRAAAQEFINRTLVDNAKAGKFVVRLKGGDPYVFGRGFEELIACAEAGVPVTVVPGVTSAFGVPALAGVPVTHRGVAHEVVVVSGHVAPDDERSLVDWGALARLRGTVVILMGVERAAAFAAALREGRPGDTPVTVVENGSTDAQRIVRSTLDGLAEAVAAHHVRPPAIIVVGPVAGLAGELPEQA
>NZ_CP023445|6738135:6789691|6740078_6740432_+|WP_096498047.1|DBSCAN-SWA
MGLSYGMTTVDAADPRGLAAFWAGALETDAVQEYGDDGDLVMLTAEGGVRLGFQRVAEPTPGKNRVHLDFGAADLAAEVERLTGLGAVLVAERSMPGVEWVVLADPAGNQFCVSRAG
>NZ_CP023445|6738135:6789691|6764885_6765626_-|WP_096496552.1|protease|DBSCAN-SWA
MRLAVFLSVLAVLCGGGVATAAEPRVVGGTRASIAEHPWVVFLAGTTGSQFCGGTLVAPTKVVTAAHCVAGTAPERLVVVAGREDKRTQAGETLRVARIWKHPFYSSAEQGSDVAVLTLVRPVANRVLPLASADPAPGTVAKVLGWGRTAEIGAASQVLLGANVPVMSDQECAADYSRFDPAAMVCAGYPRGGIDTCQGDSGGPLVANGALVGVTSWGEGCARPGQPGVYSRITAYRALIDQQLKG
>NZ_CP023445|6738135:6789691|6764058_6764772_-|WP_096498049.1|protease|DBSCAN-SWA
MALLLTGVAVAPPAGADPRIVGGVVVDAPNPYPWVVALVDPDGRQFCGGAIISRYQVMTAAHCVSGLIGGDVLVVAGRLDVTKPGGTIHPVSGVYVHPAYRSATTGADIAYLLTSTPMPYEAIALAKPSETGLYRAGITGTAFGWGRTSESGTTSPVLRKVSVPLQTNEVCSAAYPGHYQSSSMFCAGLPNGGKDACQGDSGGPFVIAGRLAGLVSWGVGCARPEYPGVYTRVGAYT
>NZ_CP023445|6738135:6789691|6784572_6786372_-|WP_096496564.1|DBSCAN-SWA
MVLLPKLAGPVCLLLLLSGCGLFTSKPGPGDALGDFLSKVASGDTEGAARLTDDPTSAEDLLDKVRGALRPTGLTTSVDRVGDQSGATAPADATLEWQLPNEHRWKYQTSLELRREADDWKVHWAPSVVHPKLGAQQSLGFTEVKPALAPVLDRDGTALMSPETVVSVLLSPKEAGDVNAVANSLAAALSRFDGKITAKTVADGAAAVPEGQSYLVAALRDADYQSVKPAIYELPGVRFTSQVSLLAPSRDYGSQVLPAIRKSVEDTVAGEAGFRVYTANSSGQEVETLFDQQPEPAHAVPTTLSRRVQDAAEDALEPVAQPAMLVALQVGTGEVLAVAQNGPADEQGAIALTGQFPPGSTFKIVTAAAAMAAGRASADSPLPCPGRTTVDGRRIVPNDKEFDKGTIPLRSAFAFSCNTTFAQLAAELPPAALTEQAASFGLGVDFEIPAVTTITGSAPEAADVVERAEDGFGQGKVVASPFGMALVAATAAGGTMPTPTLMREQATKADRQPPAPSTAVLEPLRAMMREVVESGTATQLRGLGDVRGKTGTAQYGDGVNSHGWFVGYRGDVAFATLLLGANASTPAVDATGRFLRAVG
>NZ_CP023445|6738135:6789691|6761956_6762409_-|WP_096496549.1|DBSCAN-SWA
MTQHHPATLRRQWAADLTATQLYALLKLRVDVFVVEQNCPYPELDGRDLEPGTRHLWLEEDGEPQAYLRLLEEPGGVLRVGRVVTARTARGKGFSRRLMVAAMAEIGDAEAVLDGQTYVVDFYASFGFAPEGEEFIEDGIPHLRMRRPRR
>NZ_CP023445|6738135:6789691|6743279_6743999_+|WP_041838465.1|DBSCAN-SWA
MSWSPSTTQPEQPVWPHDSLLSRLRDQARDELLAMGTVVRYAPNRDVIVQDARDTHALLLLDGVVKVQTTDETGDTALLAIKAAGDFVGEMAALDRKPRSASVITCGEVTARMISSSELMGFLHRRNEVFVEMIGMVNERLRWAIERRRDFLARAADERLAKVLAELVRTHGREEPGGWTLGFPLTKVELASIAGMKPRTAEKAFSDLRKAGVVVSHLRRDVLVPDLDALRAYAQRPPR
>NZ_CP023445|6738135:6789691|6774075_6774873_-|WP_096496556.1|DBSCAN-SWA
MRALAVAMTAALGLLAACSPAPEAPEAAPVPPSTTTTSTTTTPPPPPPKLFQQPYRYGTAQKEAPPQEGDLAPVVSSIETDKPYVFLTIDDGAVRHPKALQLIRDSGIEPSLFLNTTHVQPDPAYFNALRGAGAHVHAHTTDHPNLRGMGYEAQRAEICGNADHLGAALGTRPTLFRPPFGNYDLNTRRAAASCGMRAVVLWTAAVNDGVVQFQVGDRLRGGDIVLMHFRDSFVADFTAFCERAKADGMTPVLLDDFLAPPSERH
>NZ_CP023445|6738135:6789691|6788479_6789691_-|WP_096496566.1|protease|DBSCAN-SWA
MAFVLGVVLFALLIGISIALHELGHLATAKAFGMKVTRYYIGFGPRIWSTRKGETEYGLKAIPAGGFCEIVGMTALDELPPEDEKRAFYRQKTWKRVVVLSAGSITHFIVGFVVLYAMAATIGLPDIRDEAVVSKVSQCVPATAAEAKKENPTCAPTDPTPGVSAGVQQGDRILAVGGQRLPTWIEVQKKIQQSSGPTEVVVLRGDDEVTLTIDIPRVERELRRADGSTYVDTVGVIGVAKSRLYEYNALTAFGGATKYTGDMFANTWRGLMKFPEKIPMVIKAIGGGERDPEAPVSVVGASILGGDAVSAGLWHFFWLMLAGLNFFIGVFNLLPLLPLDGGHIAVNLYERVRDWVRKLRGKPAGPPVNYLRLLPLTYFAIFVGGAITLLTITADIVNPIRLP
>NZ_CP023445|6738135:6789691|6756612_6758646_-|WP_096496545.1|DBSCAN-SWA
MGARFPFSAVVGHDDLRLALLLNAVHPGVGGVLVRGEKGTAKSTVVRALAALLPDLAVVPGCRFGCEPGVDADCPDGPHPAGAPGADPAAEHRPARLVELPVGATEDRLIGSLDLERALTEGVRAYQPGLLAAAHRGVLYVDEVNLLQDHLVDLLLDAAAMGRAHVEREGVSVSHPASFLLVGTMNPEEGELRPQLLDRFGLTVAVKAARDVPTRAEVIRRRLAYEADPAGFAKAWEAEDAALAARIAQARAALPSVALPDAELRRIAGICAAFEVDGMRADLVVARAATAHAAWRGAEAVQEQDVEAAVRLALPHRKRRDPFDEPGMEEEQLSDAMRQGAEHAQDEPDDDPDGPDDGGPDGGPDGGGPDDGQGPDQPQGPQEPGGEQPGPSQQDGKQGGSGGTRTHSPSPAFRTRLLQVPGVGEGASGKRSRARSRSGRAVRPSTTEGSGLHLVATLTAAAPHQGARGRTGPGLLLRGEDLRKAVREGTEGNLVLFVVDASGSMAARQRMSAVSGAVISLLRDAYQRRDKVGVITFRGSEAETALPPTTSVDAAAARLRALRTGGRTPLADGLLRARRLLQSEKVRDPRRRPLLVLLTDGRATATGAGGDPVRDALRAAGLLAADRVASVVVDCESGHVRLGMAARVAAALDGACLRLEELSADQVAGVVRAARAA
>NZ_CP023445|6738135:6789691|6754509_6755907_-|WP_096496543.1|DBSCAN-SWA
MSALVVAAPASGSGKTTVATGLMAALRRAGDAVAPFKVGPDYIDPGYHALATGRPGRNLDPVMVGEHRVPELFAHGARGADLAVVEGVMGLFDGRIDTDGVGSTAHVAKLLGAPVLFVVDARGQSRSLAALLHGFRGYDPGVRLGGVVLNQVGSPRHEQVLRSACADVGLDVLGVLPRDDRFALPSRHLGLVTAAEHGHEAVAAVEAVADAVGAHVDLAAVRALAATANPVAARAWDPEAEIAAAIENPGAATVPGARRPVIAVAGGPAFTFGYAEHPELLRAAGAEVVVFDPLRDETLPASTSGLLLPGGFPEQHVAELSANEPLRAAITALARAGAPVHAECGGLLYLAKSLDGAPMCGVVDSEAAMTPRLVLGYRDAVAPVDSVLLPVGARVTGHEFHRTALSTPHGADPAWRWRGHDGRPAAEGFVLGNVHASYLHTHPASIPGAAHRFTAACAAWGHPPA
>NZ_CP023445|6738135:6789691|6759874_6760561_+|WP_096496547.1|DBSCAN-SWA
MTADDRPYHHGRLREALLDAAWRSVREHGAEQLSLRELAREVGVSHAAPRRHFPDRQALLDALAIAGFERMDAELRTAVAGAGADYRDRLVAATRAYFRFAVDDPALLELMYTGKHRPGADAVVAAVAAPLGLLEAMLAEGLERGELGDGDPERIGVLMFATVHGLAAMVKGRMVDREVAGGLVDDAVVRFLTGGVPSAAGAPGAAGAPGAAGAPGAAGGALWTCPRP
>NZ_CP023445|6738135:6789691|6752355_6753204_-|WP_096496541.1|DBSCAN-SWA
MDVPALHRFLTDTGRTWSAVTVVDAAEHGLAHARNVCLARSSVLVANADPAALARGLAGWRRTLVVPGAPGPSTVDPAEVALRSWPEPLPVLCLAEQPLLPDTSRWALPDDEFSHRGDGLVATAEVRALVLAKLGPRSGALVWDVAAGPGAVAVECARLGAAVVAVERDPVQCVRIIANASAHHVDVRVVESDVELAPHDLPRPDAVFVGGGGPGAVRTCAALGARRVVVATTRLDAVLPSHDALRDGGYAVSGTQLSAARLEDDHLRAVDPVTVLWAERPA
>NZ_CP023445|6738135:6789691|6781338_6782904_-|WP_096498053.1|DBSCAN-SWA
MAALGRRWRGAAVSGAVLVAGTTSDAGKSVLVAGLCRWLAREGVRVAPFKAQNMSNNSAVTPDGGEIGRAQALQAAACGLEPSVRFNPVLLKPGGDRSSQVVVLGKVAGEVSAMSYRERKAELMTVVLDTLAGLRADYEAVVCEGAGSPAEINLRATDIANMGLARAAGLPVLVVGDIDRGGVLAHLFGTLALLDPADQALVAGFVVNKFRGDPALLEPGLRQLRELTGRPVHGVLPWREELWLDAEDSLSYAADGVIGRPQAPVGRQWLRVAVVRLPRISNATDVEALACEPGVSVRFVTEPSRLADADLVVLPGSKATVSDLAWLRRTGLADAIAAHDGPVLGVCGGYQMLARSIDDPVESGAGAVPGLGLLDVDVVFEPEKALHRPTGVALGEPVTGYEIHHGRVARRADDLPGLVELPDGEVEGAVRGRVMGTHWHGLLENNAFRRAFLRHVAGLAGRDGFAVAPDTDFAARREAQLDLLGDLVVDHLDTGAVRALLERGVPGGLRVVPPAGAPAVG
>NZ_CP023445|6738135:6789691|6742458_6743148_+|WP_096496536.1|DBSCAN-SWA
MTGADPVWPSTSLLGRVREPARTDLLALGTRVPYGPDKEVIVQDARDTHVLLLLSGMVKVQAVDEDGEHALLDIRIAGDVVGEMAALSGKPRSATVRTCGEVVARAITRADFQALLLRRPEVAMELVLVVGERLRWSIDRRRDFLSCPAPVRVARVLVELVQTYGRQDKDAWRLGIPLTKVELASIAGMKPRTAEKAFSDLRHAGVVVSNLRRDVLVPDLRALRRYAGS
>NZ_CP023445|6738135:6789691|6763424_6764039_+|WP_096496551.1|DBSCAN-SWA
MQFDLTTLPAFLIACAVVVLTPGVDSFLLLRTSMRSGTRAGLLALAGIHTAAAIQVAVVISGLGVVIAGFPPALTALRWIGAAYLLYLALSITRDLVRNRGRAPEEGEVVADRPFRRGFLTNITNPKMLLFSLAFLPQFIGSGDPTPQLAMLAAVFLALAAAWEGTIVLAASAVGGRLRKPGVTTALDVVCAAVFATMSVGLVL
>NZ_CP023445|6738135:6789691|6744851_6745757_+|WP_096498048.1|DBSCAN-SWA
MDDYGPREVRTRVRVVRDDEENVRRGRLTEEAKKRLGESRQLTGPEDGDRWSTWGSADQGPAPHPAWLVTDLGAVDRELGLIKSGKEADVSLLERATPDRSCLLAAKRYRDNDHRLFHRDAGYLEGRRERRSREARAMSRRSAFGRNLIAERWAVAEFAALGALWQRGVPVPYPVQRDGTEVLMEFIGDGAQAAPRLAQTRPEPDALVDLWRQLGSALTGMAAAGYAHGDLSPFNLVVHDDRLVVIDLPQLVDLVANPRGAEFLARDVRVVAEWFTARGLPAELADPVELTADLLREAGLA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_096496534.1|6738135_6739881_-|tRNA	proline--tRNA ligase	NA	NA	NA	NA
WP_096498047.1|6740078_6740432_+	VOC family protein	NA	NA	NA	NA
WP_096496535.1|6740693_6741461_+	peroxide stress protein YaaA	NA	NA	NA	NA
WP_096496536.1|6742458_6743148_+	Crp/Fnr family transcriptional regulator	NA	NA	NA	NA
WP_041838465.1|6743279_6743999_+	Crp/Fnr family transcriptional regulator	NA	NA	NA	NA
WP_096498048.1|6744851_6745757_+	kinase	NA	NA	NA	NA
WP_096496537.1|6746551_6748057_+	DEAD/DEAH box helicase	Q5GF26	Diachasmimorpha_longicaudata_entomopoxvirus	3.7e-41	28.3
WP_096496538.1|6748364_6749582_-	uroporphyrinogen-III C-methyltransferase	NA	NA	NA	NA
WP_096496539.1|6749890_6750676_-|protease	serine protease	Q0ZP54	Neodiprion_abietis_NPV	3.1e-23	33.8
WP_096496540.1|6750764_6752024_-	cobalamin biosynthesis protein CbiG	NA	NA	NA	NA
WP_096496541.1|6752355_6753204_-	hypothetical protein	NA	NA	NA	NA
WP_096496542.1|6753208_6754339_-	cobalt-precorrin-4 C(11)-methyltransferase	NA	NA	NA	NA
WP_096496543.1|6754509_6755907_-	cobyrinate a,c-diamide synthase	NA	NA	NA	NA
WP_096496544.1|6755903_6756518_-	cob(I)yrinic acid a,c-diamide adenosyltransferase	NA	NA	NA	NA
WP_096496545.1|6756612_6758646_-	putative cobaltochelatase	NA	NA	NA	NA
WP_096496546.1|6758919_6759813_-	SDR family NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_096496547.1|6759874_6760561_+	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_096496548.1|6760827_6762006_+	8-amino-7-oxononanoate synthase	NA	NA	NA	NA
WP_096496549.1|6761956_6762409_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_096496550.1|6762507_6763257_-|protease	serine protease	Q6JKF3	Neodiprion_sertifer_nucleopolyhedrovirus	1.1e-22	35.2
WP_096496551.1|6763424_6764039_+	LysE family translocator	NA	NA	NA	NA
WP_096498049.1|6764058_6764772_-|protease	serine protease	Q0ZP54	Neodiprion_abietis_NPV	6.1e-26	36.2
WP_096496552.1|6764885_6765626_-|protease	serine protease	I6WTR7	Cotesia_sesamiae_Mombasa_bracovirus	1.1e-17	30.3
WP_096496553.1|6765794_6766829_-|protease	M48 family metalloprotease	NA	NA	NA	NA
WP_096498050.1|6766939_6767839_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_096498051.1|6767868_6768501_+	CatB-related O-acetyltransferase	A0A2R8FE91	Brazilian_cedratvirus	4.4e-20	42.3
WP_096496554.1|6768559_6770923_-	endopeptidase La	A0A0R6PGP8	Moraxella_phage	4.7e-139	45.0
WP_096496555.1|6771094_6771895_+	hypothetical protein	NA	NA	NA	NA
WP_096498052.1|6771969_6773904_-	patatin	NA	NA	NA	NA
WP_096496556.1|6774075_6774873_-	polysaccharide deacetylase family protein	NA	NA	NA	NA
WP_096496557.1|6775005_6775533_+	YbhB/YbcL family Raf kinase inhibitor-like protein	NA	NA	NA	NA
WP_096496558.1|6775574_6776954_+	mycothione reductase	A0A2K5B2C5	Erysipelothrix_phage	4.9e-40	26.5
WP_096496559.1|6777019_6778378_-	MFS transporter	NA	NA	NA	NA
WP_015804574.1|6778461_6779133_+	FadR family transcriptional regulator	NA	NA	NA	NA
WP_096496560.1|6779332_6780247_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_096496561.1|6780321_6781215_+	EamA family transporter	NA	NA	NA	NA
WP_096498053.1|6781338_6782904_-	cobyric acid synthase	NA	NA	NA	NA
WP_096496562.1|6782914_6783622_+	hypothetical protein	NA	NA	NA	NA
WP_096496563.1|6783666_6784524_-	type I methionyl aminopeptidase	NA	NA	NA	NA
WP_096496564.1|6784572_6786372_-	penicillin-binding protein	NA	NA	NA	NA
WP_096498054.1|6786389_6787241_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_096496565.1|6787294_6788452_-	flavodoxin-dependent (E)-4-hydroxy-3-methylbut-2-enyl-diphosphate synthase	NA	NA	NA	NA
WP_096496566.1|6788479_6789691_-|protease	site-2 protease family protein	NA	NA	NA	NA