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_CP019798	Streptomyces sp. fd1-xmd chromosome, complete genome	13 crisprs	cas5,cas7,cse2gr11,cas8e,cas3,csa3,WYL,DEDDh,cas4,Cas9_archaeal,c2c9_V-U4,DinG	5	13	2	0

1. NZ_CP019798

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP019798_1

• CRISPR_ID: NZ_CP019798_1
• CRISPR_location: 1068236-1068634
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 8 spacers

Consensus repeat of NZ_CP019798_1

Consensus_repeat	Method
GGNGANNNCGACGGGGAC	CRT

spacers of NZ_CP019798_1

>1.1|1068254|24|NZ_CP019798|CRT
CCCGACGGCGTCGGCGGTTCCGAC
>1.2|1068296|36|NZ_CP019798|CRT
TTGGACGGGGTGGGCGACTCCGAGGCCGTCGGTGTG
>1.3|1068350|18|NZ_CP019798|CRT
GGCGTCGGCGAGGGCTTC
>1.4|1068386|36|NZ_CP019798|CRT
CCGGAGGGCGACTTCGACGGGGTCGGCGAACCCGAG
>1.5|1068440|30|NZ_CP019798|CRT
GGCGAACCGGAGGGCGTCGGCGAACCCGAG
>1.6|1068488|30|NZ_CP019798|CRT
TTCGACGGCGACTGCGATCCCGAGTGCGTG
>1.7|1068536|18|NZ_CP019798|CRT
TTCGACCCCGTGGGCGTG
>1.8|1068572|45|NZ_CP019798|CRT
CCGGTCGGCGGCGTCGGCCCGGTGCGCGTCGGCGTGGCCGGGCTG

CRISPR arrays and Neighbor proteins around NZ_CP019798_1

CRISPR arrays

The CRISPR arrays of NZ_CP019798_1

>merge|NZ_CP019798|1|1068236-1068634|CRT
GGGGACCCCGAGGGGGAACCCGACGGCGTCGGCGGTTCCGACGGTGACCCCGAAGGGGGCTTGGACGGGGTGGGCGACTCCGAGGCCGTCGGTGTGGGTGAGCCCGACGCGGACGGCGTCGGCGAGGGCTTCGGCGAGACCGACGGGGATCCGGAGGGCGACTTCGACGGGGTCGGCGAACCCGAGGGCGACTTCGACGGGGACGGCGAACCGGAGGGCGTCGGCGAACCCGAGGGCGTCTTCGACGGGGACTTCGACGGCGACTGCGATCCCGAGTGCGTGGGGGACTTCGACGGGGACTTCGACCCCGTGGGCGTGGGCGACTTCGACGGCGACCCGGTCGGCGGCGTCGGCCCGGTGCGCGTCGGCGTGGCCGGGCTGGGCGTGGTCGGCGGCGTC

>NZ_CP019798|1|1|1068236-1068634|CRT
GGGGACCCCGAGGGGGAA	CCCGACGGCGTCGGCGGTTCCGAC
GGTGACCCCGAAGGGGGC	TTGGACGGGGTGGGCGACTCCGAGGCCGTCGGTGTG
GGTGAGCCCGACGCGGAC	GGCGTCGGCGAGGGCTTC
GGCGAGACCGACGGGGAT	CCGGAGGGCGACTTCGACGGGGTCGGCGAACCCGAG
GGCGACTTCGACGGGGAC	GGCGAACCGGAGGGCGTCGGCGAACCCGAG
GGCGTCTTCGACGGGGAC	TTCGACGGCGACTGCGATCCCGAGTGCGTG
GGGGACTTCGACGGGGAC	TTCGACCCCGTGGGCGTG
GGCGACTTCGACGGCGAC	CCGGTCGGCGGCGTCGGCCCGGTGCGCGTCGGCGTGGCCGGGCTG
GGCGTGGTCGGCGGCGTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078093618.1|1062216_1064184_+|molybdate-ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|226361
NZ_CP019798.1|WP_078093616.1|1060633_1061029_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|133390
NZ_CP019798.1|WP_076046054.1|1060098_1060488_-|RNA-binding-S4-domain-containing-protein	unknown	unknown	gnl|CDD|224109
NZ_CP019798.1|WP_078093619.1|1064621_1066703_-|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl|CDD|369272
NZ_CP019798.1|WP_060180343.1|1058789_1059191_+|PTS-fructose-transporter-subunit-IIA	unknown	unknown	gnl|CDD|131417
NZ_CP019798.1|WP_078093622.1|1075874_1077125_+|Tm-1-like-ATP-binding-domain-containing-protein	unknown	unknown	gnl|CDD|350626
NZ_CP019798.1|WP_078093620.1|1069700_1070984_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_173675314.1|1054765_1055650_-|CPBP-family-intramembrane-metalloprotease	unknown	unknown	gnl|CDD|376806
NZ_CP019798.1|WP_076046068.1|1074281_1075328_+|cation-transporter	unknown	unknown	gnl|CDD|224151
NZ_CP019798.1|WP_030848901.1|1075358_1075826_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|240020
NZ_CP019798.1|WP_060180313.1|1066824_1067040_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_076046076.1|1079693_1080983_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|223540
NZ_CP019798.1|WP_078093623.1|1077267_1078893_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP019798.1|WP_030848889.1|1071057_1071717_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078096098.1|1058178_1058763_+|dihydroxyacetone-kinase-subunit-L	unknown	unknown	gnl|CDD|274099
NZ_CP019798.1|WP_078093621.1|1071722_1074101_-|ATP-transporter-ATP-binding-protein/permease	unknown	unknown	gnl|CDD|224054
NZ_CP019798.1|WP_078093625.1|1081143_1082598_+|glycosyltransferase-family-39-protein	unknown	unknown	gnl|CDD|227621
NZ_CP019798.1|WP_078093617.1|1061172_1061994_+|molybdate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270256
NZ_CP019798.1|WP_078093624.1|1078889_1079501_+|hypothetical-protein	unknown	unknown	gnl|CDD|235899
NZ_CP019798.1|WP_078093615.1|1055916_1058001_-|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|369272

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_078093618.1|1062216_1064184_+|molybdate-ABC-transporter-permease-subunit	gnl|CDD|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	3.56913e-80
NZ_CP019798.1|WP_078093616.1|1060633_1061029_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|133390	cd04762, HTH_MerR-trunc, Helix-Turn-Helix DNA binding domain of truncated MerR-like proteins. Proteins in this family mostly have a truncated helix-turn-helix (HTH) MerR-like domain. They lack a portion of the C-terminal region, called Wing 2 and the long dimerization helix that is typically present in MerR-like proteins. These truncated domains are found in response regulator receiver (REC) domain proteins (i.e., CheY), cytosine-C5 specific DNA methylases, IS607 transposase-like proteins, and RacA, a bacterial protein that anchors chromosomes to cell poles.	3.66676e-13
NZ_CP019798.1|WP_076046054.1|1060098_1060488_-|RNA-binding-S4-domain-containing-protein	gnl|CDD|224109	COG1188, COG1188, Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) [Translation, ribosomal structure and biogenesis].	3.24649e-23
NZ_CP019798.1|WP_078093619.1|1064621_1066703_-|SpoIIE-family-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	6.1183e-48
NZ_CP019798.1|WP_060180343.1|1058789_1059191_+|PTS-fructose-transporter-subunit-IIA	gnl|CDD|131417	TIGR02364, dha_pts, dihydroxyacetone kinase, phosphotransfer subunit. In E. coli and many other bacteria, unlike the yeasts and a few bacteria such as Citrobacter freundii, the dihydroxyacetone kinase (also called glycerone kinase) transfers a phosphate from a phosphoprotein rather than from ATP and contains multiple subunits. This protein, which resembles proteins of PTS transport systems, is found with its gene adjacent to.	5.02177e-22
NZ_CP019798.1|WP_078093622.1|1075874_1077125_+|Tm-1-like-ATP-binding-domain-containing-protein	gnl|CDD|350626	cd15488, Tm-1-like, ATP-binding domain found in plant Tm-1-like (Tm-1L) and similar proteins. Members of this family have been annotated as UPF0261-domain containing proteins. They are found in plants, fungi, bacteria, and archaea. A three-dimensional structure of a complex between the tomato resistance gene product Tm-1 and tomato mosaic virus helicase reveals an organization encompassing two distinct structurally similar domains and an ATP-binding site present in the N-terminal subdomain. The Tm-1-like domain is found co-occurring with a C-terminal TIM-barrel signal transduction (TBST) domain in some plant proteins like Tm-1, and with an N-terminal ABC-transporter ATP-binding domain in a few bacterial proteins.	0
NZ_CP019798.1|WP_173675314.1|1054765_1055650_-|CPBP-family-intramembrane-metalloprotease	gnl|CDD|376806	pfam02517, Abi, CAAX protease self-immunity. Members of this family are probably proteases (after a isoprenyl group is attached to the Cys residue in the C-terminal CAAX motif of a protein to attach it to the membrane, the AAX tripeptide being removed by one of the CAAX prenyl proteases). The family contains the CAAX prenyl protease. The proteins contain a highly conserved Glu-Glu motif at the amino end of the alignment. The alignment also contains two histidine residues that may be involved in zinc binding. While they are involved in membrane anchoring of proteins in eukaryotes, little is known about their function in prokaryotes. In some known bacteriocin loci, Abi genes have been found downstream of bacteriocin structural genes where they are probably involved in self-immunity. Investigation of the bacteriocin-like loci in the Gram positive bacteria locus from Lactobacillus sakei 23K confirmed that the bacteriocin-like genes (sak23Kalphabeta) exhibited antimicrobial activity when expressed in a heterologous host and that the associated Abi gene (sak23Ki) conferred immunity against the cognate bacteriocin. Interestingly, the immunity genes from three similar systems conferred a high degree of cross-immunity against each other's bacteriocins, suggesting the recognition of a common receptor. Site-directed mutagenesis demonstrated that the conserved motifs constituting the putative proteolytic active site of the Abi proteins are essential for the immunity function of Sak23Ki - thus a new concept in self-immunity.	2.63207e-11
NZ_CP019798.1|WP_076046068.1|1074281_1075328_+|cation-transporter	gnl|CDD|224151	COG1230, CzcD, Co/Zn/Cd efflux system component [Inorganic ion transport and metabolism].	1.0951e-83
NZ_CP019798.1|WP_030848901.1|1075358_1075826_+|NUDIX-domain-containing-protein	gnl|CDD|240020	cd04662, Nudix_Hydrolase_5, 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 and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which 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.	6.41763e-49
NZ_CP019798.1|WP_076046076.1|1079693_1080983_-|GNAT-family-N-acetyltransferase	gnl|CDD|223540	COG0464, SpoVK, ATPases of the AAA+ class [Posttranslational modification, protein turnover, chaperones].	3.15405e-47
NZ_CP019798.1|WP_078093623.1|1077267_1078893_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	1.46214e-89
NZ_CP019798.1|WP_078096098.1|1058178_1058763_+|dihydroxyacetone-kinase-subunit-L	gnl|CDD|274099	TIGR02365, dha_L_ycgS, dihydroxyacetone kinase, phosphoprotein-dependent, L subunit. Two types of dihydroxyacetone kinase (glycerone kinase) are described. In yeast and a few bacteria, e.g. Citrobacter freundii, the enzyme is a single chain that uses ATP as phosphoryl donor and is designated EC 2.7.1.29. By contract, E. coli and many other bacterial species have a multisubunit form (EC 2.7.1.-) with a phosphoprotein donor related to PTS transport proteins. This family represents the subunit homologous to the E. coli YcgS subunit.	6.72794e-70
NZ_CP019798.1|WP_078093621.1|1071722_1074101_-|ATP-transporter-ATP-binding-protein/permease	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	6.04584e-66
NZ_CP019798.1|WP_078093625.1|1081143_1082598_+|glycosyltransferase-family-39-protein	gnl|CDD|227621	COG5305, COG5305, Predicted membrane protein [Function unknown].	3.40942e-18
NZ_CP019798.1|WP_078093617.1|1061172_1061994_+|molybdate-ABC-transporter-substrate-binding-protein	gnl|CDD|270256	cd13538, PBP2_ModA_like_1, Substrate binding domain of putative molybdate-binding protein;the type 2 periplasmic binding protein fold. This subfamily contains domains found in ModA proteins of putative ABC-type transporter. Molybdate transport system is comprised of a periplasmic binding protein, an integral membrane protein, and an energizer protein. These three proteins are coded by modA, modB, and modC genes, respectively. ModA proteins serve as initial receptors in the ABC transport of molybdate mostly in eubacteria and archaea. After binding molybdate with high affinity, they interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ModA 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.	4.12087e-82
NZ_CP019798.1|WP_078093624.1|1078889_1079501_+|hypothetical-protein	gnl|CDD|235899	PRK06975, PRK06975, bifunctional uroporphyrinogen-III synthetase/uroporphyrin-III C-methyltransferase; Reviewed.	0.00312376
NZ_CP019798.1|WP_078093615.1|1055916_1058001_-|PAS-domain-S-box-protein	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	4.20493e-44

Protein sequences

>NZ_CP019798.1|WP_060180313.1|1066824_1067040_-|hypothetical-protein
MRVKRLFAASAIGVLMAGGALGAAGTASAATPTQPVSYVSGGGGWDHDKGGHHGWYDDDDDDYRGGGHGDC
>NZ_CP019798.1|WP_078093619.1|1064621_1066703_-|SpoIIE-family-protein-phosphatase
MARRGDVPEVDWPARPDTSLALNRMGTFDWDLDSGRMHLDRTALEVLDLRPDEYSGTPAGLRARIAPAEEARLDSRVAQAIKDGRSHYGAYVRSRRRDGSPAWTHIQGHILRDPGGRPYRVIGILRDAAHDPGEPGAAGEQDEGRRRMTGVVERTTAILAHARTVNDVTDILKDPQALGHLGAVSVMLGVVDGGRIHLVAEGQLGTYVPEIEYTRIDERFPMSVAVRTMQPVFILSRQEFQDSYPELWPYIEPLAVHSGVYLPLIAQGRPIGALGLLYRREGDFTAEERNLLMALGSGVAQSLQRAILFEQEHDLAEGLQRAMLPRRIPAVPGALIAVRYRSARMGRDIGGDWYDVVPLGGGRVGVMIGDVEGHDTDAAAVMGQLRIVMRAYVVEGHTPGAAMARASSFLRELETERFATCTYAEIDLTSGMLQMVRAGHLDPVVRRGDGSCHRIRVAGGLPLGLPAREPTAAAGSGYPVTSLELHPGDTLVLCTDGLVERPGADPDTGMRELMEAIHSGPADVEELADVLCDLVGDSGGRDDMALLVLRRRGTAPGRGGRPLSHRLEPGDAEAPALARHLVRAAAAAVGARDRADEIELAADELMTNALVHTDGGGHISMRTTAEGRIRVEVEDSSSALPRRRDADDWAVSGRGLMLVEQLADEWGVEPRGGGKCVWCEFVVDAEQSTGEPS
>NZ_CP019798.1|WP_078093618.1|1062216_1064184_+|molybdate-ABC-transporter-permease-subunit
MSRLRTRTRPPVALALPALLAVAFLLLPLIGVLVRTPWGDLGEHLGSPGVVEALKLSLLVSLWALGLSLLLGVPLAWLLARVRFKGKALVRSLVLLPMVLPPTVGGVALLLGFGRRGLLGPWLEDSFGLTLPFHTSGAVVAATFVAMPFLVISLEGALGGLKQSYEETAASLGASPVRVFFTVTLPMVAPGLVAGAALTWARALGEFGATITFAGNLPGTTQTLPLQVYLLLQDRPEAATSVSLLLLAIAMAVLIALRGRWTGAPVGRGAVTVSRPAPDEAPSPAAEPVGDTASAGLPPTESAGHAAQPVQHWPLHATVTGFNRLTLEAEPGTTIAVVGENGAGKTTLLRALLGLTPRAHADLRLGDADVTALPPHKRQVAWVPQDGALFPHLSALANTAYGLRARRVPRADARREAQAWLDRLGVGHLAHRKPSQLSGGQAQRVALARALAARPRLLLLDEPLAALDQTTRARVRHTLRTHLAGFGGVCLIVTHDPVEAVSLADRVLVLADGRALQDAPPAEVSRHPRSRWVARMLGRNAWPGIASGGGLALAAGGRLVVAEALPDGAEALAIIAPEAVSVHRDRPGGSPRNVWPGTVREITAVGSRLRVLIASPEAPDLVAEITPDAAAELGLADGCAVWTSVKATEVTLVRL
>NZ_CP019798.1|WP_078093617.1|1061172_1061994_+|molybdate-ABC-transporter-substrate-binding-protein
MPPTPLRRRRTAAAAAALSAALLAALTGCGSGDDKPAASDSGSAAPSASAASRADLTVLAASSLTDVFKAAGEAYQKSHPGTKVTFSFAGSQELAAQVKQGAPADALVTADTRTMDGLKAETGDAKIIAKNRLVIAAGKGNPFKIDELRDLAGPKVKVVLAAPEVPVGRYSKQILDAQRIEVKPVSQEPNVRAVLSKVELGEADAGLVYRTDSAKAGDKVVTVEIPDEQNAVASYPAATLKQSKNADAAAAFVAWLSTPEAQKILQDAGFQQP
>NZ_CP019798.1|WP_078093616.1|1060633_1061029_+|helix-turn-helix-transcriptional-regulator
MQSYTFGQAARLLGVSPDTARRWADAGRVVTHRDEVGRRLINGRDLAAFSGEVGQGAHAEDAEPYTSARNAFPGIVTAVRLGDVCAQVDIQAGPHRLVSLLTREAAEELGLEVGMRATARVKSTSVHVDRA
>NZ_CP019798.1|WP_076046054.1|1060098_1060488_-|RNA-binding-S4-domain-containing-protein
MADEVSGTETGTVRVDAWIWSVRLTKTRSIAATACRAGHVKVNGERAKPAQAIRAGDEVRLFHAGRERIVVVKRPVSKRVGAPVAAECLIDKSPPPPTPVEAAVVGIRDRGTGRPTKRDRREIQSLRGR
>NZ_CP019798.1|WP_060180343.1|1058789_1059191_+|PTS-fructose-transporter-subunit-IIA
MPALVGVVLVSHSAPVAESVAELARGLAAGGPVAPVAAAGGTAAGGLGTSAERVVAAAREVDRGAGVALIADLGSSVLTVKALLLEDELPPDARLVDAPFVEGAVAALVAASAGAPLAQVAEAAAEAYAYRKV
>NZ_CP019798.1|WP_078096098.1|1058178_1058763_+|dihydroxyacetone-kinase-subunit-L
MAAAAAVVEREADRLTELDSPIGDADHGSNLLRGFTAVRTALDAEGPAAPGAVLQLAGRTLISTVGGASGPLYGMLLRRTGKELGEAPEVSDEELREALDKGVGAVAQLGGAAPGDKTMLDALLPGVAALATSYRAAADAAQDGALATVPMQARKGRASYLGERSIGHQDPGATSSALLMGALADAAERVEGAR
>NZ_CP019798.1|WP_078093615.1|1055916_1058001_-|PAS-domain-S-box-protein
MRSTGSARFGHVVGCLLLRDSTSARRSVAATTEEPFRALLEAAPDAMVIVDDSGVIRLVNAQTEALFGHPRRELLGRHIEILVPERFRGQHPGHRVGYAASRQVRPMGAGLELYGLRRDGREFPVEISLSPLETPEGLLISAAVRDVSERRAAEERFRALLEAAPDAMVIVDERGAIQLVNAQTEALFGYAREDLLGRPVEVLVPARFRGHHSDFRHGYFVNRKTRPMGAGLELYGLRRDGGEFPVEISLSPLETPDGTLVSAAIRDVTERKSAEEMLAKLYEQQRHVALTLQRSLMGSPPDVPGMPTASRYFPARQGAGVGGDWFDLIPLGGGRVGVMVGDVMGRGLDAAAVMGQLRSASHALAKTGMPPWQLMRALDAVVSELPDQFVTCCYLVVDADSAEITMCSAGHLPVLLVAPCGEVTRLPVEVSVPLGVGEVPHHETRHTVEPGSVLALYTDGLVETPDSDIEGQVDGLAAALEKAVATTDSLEAAADRLLGELLPEVDENPDDVTLLLVRIPDTPVTSQSMLLAADPSSVGAGRRFLRSTLALWGKDDDQLRDTACLLTSELLSNAVNHSCGPVRLRLRQAGRELSVEVCDGSPVLPQARFAAPDAESGRGLLLVDSLAASWGTLPTAEGKAVWFSLPLPAPRPAPPSDRPAEGAACGRPADPRATTNPRATADPCARTDPRAKTD
>NZ_CP019798.1|WP_173675314.1|1054765_1055650_-|CPBP-family-intramembrane-metalloprotease
MGEFLLVVVGNLAVPLVVVAFGALAWYVLGLDFAPEDGDRILADPLADEALALLSIATGIPVVLLAVRWCGSRPAGTAASVVGRLRWGWLARCAAVAFPLIVLQMGGLALWGYLSDGEESLAGDFPGWSGFALALVVLWALIPFQAAAEEFVFRGWLAQFFGGFLRSPWPGTVIASALFAAAHGFGEWSGFALLFYSAMWWGWLTVRTGGLEAVIAVHVANNMTAYAITAALGQLAESGNAADAPWQALVLELVAAPAYCLLIAKLATAHGVRRRSPATPAGSAEPDGRAEPAG
>NZ_CP019798.1|WP_078093620.1|1069700_1070984_+|hypothetical-protein
MSQTSGTASSGGSARAWRDALVTVVAGFAAMIAVAAAGLACAGAGDLPEGAFPRVLAAVVVMAAGGTVEVSGDAGLLAGVDASLSVLPLSVSLAGALAAGWCFLRPLHNRAVAGPRELLGRAVPLVVLWLLALTGAAAVARQDFGISTGDSALGVIGELLDAEPKVGFRADVPATLLLGLVWILGLLLIALLVSRRAPLPAGLVRFHTAVRPAAFATTLLLLAYVVIGVVVGLVVAATQGHAGRTLAVVLLGLPNLVWIALTLGFGGAWEARVEGAFGLPVPRLLDEVLRDADGAPVDVATLAARDPRAWWLVVAAAVLLLGTGVLAAVRSPSHVRPWQHALHLGAALALATLAVCLLARIHAVYGLSLLGIGEVDALGGQVLLDPVLWRTVGLGLLWGAVAGFLGGVLARPLHRRGRVDEPAAQRG
>NZ_CP019798.1|WP_030848889.1|1071057_1071717_-|hypothetical-protein
MSSMDPGIAVADFRPTHVVPPPGLSAWEAPDVSRPTASLDAFLPVQLLSRRGEWGEILCANGWSAWVDGRLLVAVPQPPPTAGERPSVRAEDPRPLLERGAHALERYRHAVDELASGRADTDAFRRSLRGLRVGVVVDGESVWLYDESSGRWMYGDGTRLATYAVTDALGTAHGSPQAGPDDAGRAGAGPDAPPAGPEAGGADRATPTRIVDTHDPELE
>NZ_CP019798.1|WP_078093621.1|1071722_1074101_-|ATP-transporter-ATP-binding-protein/permease
MVQRPGVPTAPELVLETATGSTPMSPGRTYRVGRDPLCEVCFEDGRVSWHHAVLRPDGDHWTVEDEDSTNGTWADGHRVHEWSVGAGSELRFGDAQDGPRAVLLAPGPASEAAGGRPSGVADPSLTTTFRQPSAVLPLPARTTVRIGRATDNDLVIDELDVSRRHAELRALAGGGYEIADLGSHNGTYLNGAPVTGTAPLTEGDIVGIGHLAFCLVGDRLQEYEDTGEVTLDVQGLTVAVDRGRKTLLDQVSFPVGAKCLLAVIGPSGAGKSTLLGALTGLRPADHGTVLYDGRDLYRDYAELRSRIGLVPQDDILHSQLTVRRALLYAAELRFPQDTAKAERRRRVDEVIGELGLEQRADQPIHSLSGGQRKRVSVALELLTKPSLLFLDEPTSGLDPGMDRSVMHMLRGLADDGRTVIVVTHSVLSLDVCDRLLVLAPGGRIAYYGPPAQTLGFFGFSQWPEAFEAFENQRGRDWAAEYAASAAHRTYVLGAARQPWYGEYPAAAGAAAAPDSVPPPPKAQSWGSQLSTLVRRYAAALAADRTFLAIMIALPFVMGAMARALAGSRLTQETAINALLILSVGGVLTGAANAVRELVKERVIYRRERAVGLSRSAYLMSKVVVLGAVTVTQAVVLTLVALYGVDLNAPGGHGVLLDPLVEITIAVALLAFSAMMLGLLVSALVRKEEVTMPLLVLLAIVQVVFCGALLELDGVPVIGQLAWLVPSRWALGAMAGTIDLGAIVPGALTDDPLFAHRPAVWLLNLGMLVVLSVLFGLLVARLLRRHEPVIMRK
>NZ_CP019798.1|WP_076046068.1|1074281_1075328_+|cation-transporter
MTGHDHGHDDHGHGHSHGHGHDGHGHGPGGHSHGVAADADRRWLAVALGLIGGFMAVEVVIGVMAHSLALISDAAHMLTDAVSIVLALIAMRLAARPARGGFTYGLKRAEILSAQANGLTLLLLAVWLAYEAVRRLMDPPPVEGGLVLVTALAGIVVNVAAAWCISRANRSSLAVEGAYQHVLNDLFAFIGTAVAGLIVMTTGFRQADAIATLVVVVLMVRAGYGLVRDSGRIFLEAAPAHVDPDAVGDRLVGHPPVTEVHDLHIWTITSGQAALSAHVLVEPAGDCHAVRRELEQLLEKEYGITHTTLQVDHVQDALLSVGRHGEAPFDPHCADAHGPVHREGPHDH
>NZ_CP019798.1|WP_030848901.1|1075358_1075826_+|NUDIX-domain-containing-protein
MTYKRSAGLLLFRRTEPGIEVLLGHMGGPLWSGRTSGDWAIPKGEYGPEETPRDAARREFTEEIGLPPPEGEYLPLGEVRLSSGKLVTIWAVEADLDPALMVPGTFTLEWPPHSGNEQEFPELDRVAWCTPEMAQSMLIPSQLPFLERLLVLLKA
>NZ_CP019798.1|WP_078093622.1|1075874_1077125_+|Tm-1-like-ATP-binding-domain-containing-protein
MTNVVLVGTLDTKGVEYGWLRERLLRAGVEVVLVDTGIMGEPRVAADVSRAAVARAAGTELSLLRSAADRGAAVTTMARGAEATLLRLHAEGRLHGVLAIGGSGGTSIATRAMRALPLGVPKLMVSSMASGDTAPYVGSSDITMMYSVVDIAGINSVSAPILANAVAAIAGMAGSFARASAEHPPRLGAGPAPLVAASMAGVTTSGVDAARERLTELGYEVLVFHVSGTGGRTLETLAAQGIFAGVLDLTLSELADDLCGGILTAGPDRLSAAGRAGVPQVVSLGALDMVKFGPLESLPQRVLDRGVHVHNPSITVIRTSEAECAELGRRVAAKLRAATGPTAVCVPLRGLSTLGAPGGPYHDPRADRALFSALREGLRGSAARLYDYDTHINDPAFGRAAADRLHAMIAAVPAAA
>NZ_CP019798.1|WP_078093623.1|1077267_1078893_+|serine/threonine-protein-kinase
MDDTRAAWSVPGYTEVRELGSGGSGRVVLAVHDATGTAVAVKYLSDRLREDPAFVGEFRAEARLLGGLESPYVVRLYEYVEAPGGAAIVMELVDGISLRALLKQSGRADAEAALVVLKGSLLGLASAHRAGVVHRDYKPENVLVAADGSSKLVDFGIAANRGSTPGVAGTPAYMAPEQWQGRPASPAADVYAATATFFECLTGRKPYDGENFAELAVQHIEAPVPETEAPEPVRPLIRRGLAKAPEQRPENAEAFVAELEDVALAAYGPEWEERGQRKLAALAALLPLLFPSAGAPAAGTTAVATTKLDGGSGWAPGRRGWIAAGASLILGAVLVFTTDAIGAAPGGASALSAFATTSATPAGSASPTPDASASASASPSPSPSASASPSPSPSASASPSESVWPSPSPSPTTPTPTPTVSRSPTPSPTPTLPLRVTNVAVSLKTSVYRGDAAITVSSQGTGPVTVVVEWFLGGSQGSFSVPDGTESFTVQAGSTVTATRQHTFSRDRGCYGGVRVTTKPAAGNKSASASQYLPRCVEVPR
>NZ_CP019798.1|WP_078093624.1|1078889_1079501_+|hypothetical-protein
MSDSRAPEGDDYSATVLGSHWFSGPPAPAGPVEPDRVEGSVLRFGPGVTAAMPAPFPLDAAVAVAAAPRRRRGAGLRRYALAAVVLAAVLAYLGWQRFGPGIEVHDVAVSTDPAGPGCDATADVVAVVGTDGRPGTLTYRWVRSDGTKSEELTERVPRGQREARLHLLWTFQGTGNYQAKAELQLLSPAQRTASVNFTYRCSR
>NZ_CP019798.1|WP_076046076.1|1079693_1080983_-|GNAT-family-N-acetyltransferase
MNWLIHDYRESDLAAVVHLIDTTAELGQESVFSLAECISALTGRQPCVVAVHQGVPIGAALACVTGERAWVMRIAIAAGWRGRGLASALLVELERRLIAARVGRIAYVLPEEDLLGEGLLNAGYTRQPAVAYFEKTEPLHGPAAGLLDDLGGRFLPNGLWSKVAGMEKEKDLIERRVVLPLAEPERAAAHGVRPPRAITLFGPPGTGKTTFARAIASRLGWPFVELLPSRLADEGNLAAALRDAFARIAELERVLVFIDEVEEIAPVRTEPAQPGGIHGVTNELLKLIPGFREGDERLLVCATNSIRSLDPAFLRPGRFDYLIPIGTPDAGARAAIWARYTAGRADVDVSALVAATELFTPADIEHAARIAAQVSFERDLEAVGARGAAAAQLGATTQDYLEAVHQCRPTVTPAMTGEFEADITAHARF
>NZ_CP019798.1|WP_078093625.1|1081143_1082598_+|glycosyltransferase-family-39-protein
MRCHIPAARRGPLLCLVPFLWTLALGLWGLSRQDSVWRDEAATWQVAGRPAGEIWRMLGNVDAVHGLYYLLMHGLFEVFGASTTTLRMPSVLAVACAAVCVALIGRRVAGFWAGLGGALALGLLPAVQFYLQEGRPYALVAAGAGLSALLLVSLLQDRSGRRTWPRWTAYGAVVLVCALLNWLSLLALPAHAATLWWVRAGRGVWLRWAAYGSGAVAGALPLILFSRGQSDQVSWIPPLTWHMLIGPGILLAIGALGAWADRPDRSRVSAAAVGLPLLAVPQLGLIALSLVQPLFLDRYVLFAMVGLALLIGAALGAAVRACAPRFPKASALLVPGAVGVSVLALLPVELGRRAPASRVDDVLAVAGEVARLKRDGDAVLFVPAARRDTALVSPGAFTGLTDLALAESPVASATLKGEEAQPARIREALLEQRRVLLVTDSAKVAKAPSAERDKAKAEVLRERFTVVEDRQVRGRRVTVYERRG

Crispr_ID: NZ_CP019798_2

• CRISPR_ID: NZ_CP019798_2
• CRISPR_location: 1129003-1129132
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_2

Consensus_repeat	Method
GGAGCGGTGACGCACTGCCACTGCGGCTCCTTCGGCCGGTGCTTCCCGT	CRISPRCasFinder

spacers of NZ_CP019798_2

>2.1|1129052|32|NZ_CP019798|CRISPRCasFinder
GGTCGGAGCCGCCCTTGCCGGGGGGCCCGCAC

CRISPR arrays and Neighbor proteins around NZ_CP019798_2

CRISPR arrays

The CRISPR arrays of NZ_CP019798_2

>merge|NZ_CP019798|2|1129003-1129132|CRISPRCasFinder
GGAGCGGTGACGCACTGCCACTGCGGCTCCTTCGGCCGGTGCTTCCCGTGGTCGGAGCCGCCCTTGCCGGGGGGCCCGCACGGAGCGGTGACGCACTGCCACTGCGGCTCCTTCGGCCGGTGCCTCCCGT

>NZ_CP019798|2|1|1129003-1129132|CRISPRCasFinder
GGAGCGGTGACGCACTGCCACTGCGGCTCCTTCGGCCGGTGCTTCCCGT	GGTCGGAGCCGCCCTTGCCGGGGGGCCCGCAC
GGAGCGGTGACGCACTGCCACTGCGGCTCCTTCGGCCGGTGCCTCCCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078093650.1|1133520_1134543_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|369561
NZ_CP019798.1|WP_060180340.1|1122080_1123118_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP019798.1|WP_030845538.1|1125738_1126527_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	unknown	unknown	gnl|CDD|238847
NZ_CP019798.1|WP_078093653.1|1137818_1138481_+|DUF5134-domain-containing-protein	unknown	unknown	gnl|CDD|375044
NZ_CP019798.1|WP_107499845.1|1117093_1118299_-|geranylgeranyl-reductase-family-protein	unknown	unknown	gnl|CDD|273936
NZ_CP019798.1|WP_030845502.1|1137246_1137792_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP019798.1|WP_030845504.1|1136532_1137225_+|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176504
NZ_CP019798.1|WP_078093651.1|1134542_1135664_-|LLM-class-flavin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|366009
NZ_CP019798.1|WP_030845519.1|1131244_1132006_-|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|212491
NZ_CP019798.1|WP_173675202.1|1135713_1136340_+|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_CP019798.1|WP_030845541.1|1124716_1125679_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	unknown	unknown	gnl|CDD|224936
NZ_CP019798.1|WP_078093646.1|1120896_1121934_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239217
NZ_CP019798.1|WP_030845517.1|1132032_1133439_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_060179012.1|1123235_1124534_-|aldolase	unknown	unknown	unknown
NZ_CP019798.1|WP_078093648.1|1127559_1127943_-|thioredoxin-family-protein	unknown	unknown	gnl|CDD|239245
NZ_CP019798.1|WP_078096101.1|1129502_1130102_-|transglutaminase-family-protein	unknown	unknown	gnl|CDD|224224
NZ_CP019798.1|WP_030845530.1|1128172_1128895_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_CP019798.1|WP_030845522.1|1130186_1131248_-|threonine-aldolase	unknown	unknown	gnl|CDD|99748
NZ_CP019798.1|WP_078093647.1|1126727_1127267_-|flavin-reductase-family-protein	unknown	unknown	gnl|CDD|214900
NZ_CP019798.1|WP_060180337.1|1118635_1120000_+|dipeptidase	unknown	unknown	gnl|CDD|236127

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_060180340.1|1122080_1123118_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	3.41789e-100
NZ_CP019798.1|WP_030845538.1|1125738_1126527_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	gnl|CDD|238847	cd01714, ETF_beta, The electron transfer flavoprotein (ETF) serves as a specific electron acceptor for various mitochondrial dehydrogenases. ETF transfers electrons to the main respiratory chain via ETF-ubiquinone oxidoreductase. ETF is an heterodimer that consists of an alpha and a beta subunit which binds one molecule of FAD per dimer . A similar system also exists in some bacteria. The homologous pair of proteins (FixA/FixB) are essential for nitrogen fixation. The beta subunit protein is distantly related to and forms a heterodimer with the alpha subunit.	9.20497e-80
NZ_CP019798.1|WP_078093653.1|1137818_1138481_+|DUF5134-domain-containing-protein	gnl|CDD|375044	pfam17197, DUF5134, Domain of unknown function (DUF5134). Proteins in this family are uncharacterized, but have been identified as members of a gene cluster for the synthesis of the tetramic-acid antibiotic streptolydigin, which inhibits bacterial RNA polymerase (RNAP).	3.08338e-08
NZ_CP019798.1|WP_107499845.1|1117093_1118299_-|geranylgeranyl-reductase-family-protein	gnl|CDD|273936	TIGR02032, Uncharacterized_protein_MJ1520, geranylgeranyl reductase family. This model represents a subfamily which includes geranylgeranyl reductases involved in chlorophyll and bacteriochlorophyll biosynthesis as well as other related enzymes which may also act on geranylgeranyl groups or related substrates. [Biosynthesis of cofactors, prosthetic groups, and carriers, Chlorophyll and bacteriochlorphyll].	6.10403e-89
NZ_CP019798.1|WP_030845504.1|1136532_1137225_+|glycerophosphodiester-phosphodiesterase	gnl|CDD|176504	cd08561, GDPD_cytoplasmic_ScUgpQ2_like, Glycerophosphodiester phosphodiesterase domain of Streptomyces coelicolor cytoplasmic phosphodiesterases UgpQ2 and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in a group of uncharacterized cytoplasmic phosphodiesterases which predominantly exist in bacteria. The prototype of this family is a putative cytoplasmic phosphodiesterase encoded by gene ulpQ2 (SCO1419) in the Streptomyces coelicolor genome. It is distantly related to the Escherichia coli cytoplasmic phosphodiesterases UgpQ that catalyzes the hydrolysis of glycerophosphodiesters at the inner side of the cytoplasmic membrane to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols.	5.50634e-44
NZ_CP019798.1|WP_078093651.1|1134542_1135664_-|LLM-class-flavin-dependent-oxidoreductase	gnl|CDD|366009	pfam00296, Bac_luciferase, Luciferase-like monooxygenase.	9.95043e-45
NZ_CP019798.1|WP_030845502.1|1137246_1137792_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.21896e-09
NZ_CP019798.1|WP_173675202.1|1135713_1136340_+|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.0234e-11
NZ_CP019798.1|WP_030845541.1|1124716_1125679_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	gnl|CDD|224936	COG2025, FixB, Electron transfer flavoprotein, alpha subunit [Energy production and conversion].	1.68982e-103
NZ_CP019798.1|WP_078093646.1|1120896_1121934_-|NUDIX-domain-containing-protein	gnl|CDD|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes 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. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase 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 and "house-cleaning" enzymes. Substrate specificity is used to define child 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. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	2.2615e-18
NZ_CP019798.1|WP_078093650.1|1133520_1134543_-|alpha/beta-hydrolase	gnl|CDD|369561	pfam07859, Abhydrolase_3, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	5.54654e-82
NZ_CP019798.1|WP_030845522.1|1130186_1131248_-|threonine-aldolase	gnl|CDD|99748	cd06502, TA_like, Low-specificity threonine aldolase (TA). This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). TA catalyzes the conversion of L-threonine or L-allo-threonine to glycine and acetaldehyde in a secondary glycine biosynthetic pathway.	2.54169e-136
NZ_CP019798.1|WP_078093648.1|1127559_1127943_-|thioredoxin-family-protein	gnl|CDD|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	1.29941e-13
NZ_CP019798.1|WP_078096101.1|1129502_1130102_-|transglutaminase-family-protein	gnl|CDD|224224	COG1305, COG1305, Transglutaminase-like enzymes, putative cysteine proteases [Amino acid transport and metabolism].	6.41187e-10
NZ_CP019798.1|WP_030845530.1|1128172_1128895_+|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.	2.0684e-54
NZ_CP019798.1|WP_030845519.1|1131244_1132006_-|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|212491	cd05233, SDR_c, classical (c) SDRs. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	8.33492e-23
NZ_CP019798.1|WP_078093647.1|1126727_1127267_-|flavin-reductase-family-protein	gnl|CDD|214900	smart00903, Flavin_Reduct, Flavin reductase like domain. This entry represents the FMN-binding domain found in NAD(P)H-flavin oxidoreductases (flavin reductases), a class of enzymes capable of producing reduced flavin for bacterial bioluminescence and other biological processes. This domain is also found in various other oxidoreductase and monooxygenase enzymes... This domain consists of a beta-barrel with Greek key topology, and is related to the ferredoxin reductase-like FAD-binding domain. The flavin reductases have a different dimerisation mode than that found in the PNP oxidase-like family, which also carries an FMN-binding domain with a similar topology.	9.5028e-47
NZ_CP019798.1|WP_060180337.1|1118635_1120000_+|dipeptidase	gnl|CDD|236127	PRK07907, PRK07907, hypothetical protein; Provisional.	0

Protein sequences

>NZ_CP019798.1|WP_030845530.1|1128172_1128895_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MAELVYPPVIGAAHGLFRALDIRIDMKGTENIPRKGGAVLVSNHIGYLDFIFAGLTARPQKRLVRFMAKESVFRHRVSGPLMRAMKHIPVDRKQGETAYQHALESLRSGEIIGVFPEATISQSFTLKSFKSGAARMAQEAGVPLIPVALWGTQRLWTKGRPKNLKRSHIPVTMRVGEPIEAPTDQYAGAITRRLRERVQELLDAAQRAYPEKPRGPEDSWWLPAHLGGTAPTAAQVREAG
>NZ_CP019798.1|WP_078093648.1|1127559_1127943_-|thioredoxin-family-protein
MRELGREEGPAGGREGRLADRTGGAPARLGAAELGADPGRRASLVQFSSAFCQPCRATRRILAEVAGMVEGVAHIEIDAEERLDLVRALGIEKTPTVLVLDAEGRVVRRAAGMPRKVDVIAALGAAV
>NZ_CP019798.1|WP_078093647.1|1126727_1127267_-|flavin-reductase-family-protein
MSAPTAPTVPTAASPLSGTGRPGSPDLLRSVFRQHAAGVAVITAQDGGRPVGFTATSLNSVSADPPLLSFTIGTRASTWPAVRDSEYLGVHILGEHQRELAGLFARSGADRFGPDTGWAVGLHGVPVLDGVLAWLVCRVVARVPAGEHRVIIAQAVVGDPAGEGRPLLYHQGRFNALRD
>NZ_CP019798.1|WP_030845538.1|1125738_1126527_-|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein
MSLRIVVCVKYVPDATGDRQFTEDLTVNRDDVDGLLSELDEYAVEQALQISENSDDDVEITVLTVGPEDAKDALRKALSMGADKAIHVEDDDLHGTDVMGTSLVLAKAIEKAGYDLVITGMASTDGTMGVLPAILAERLGVPQATLLSEVKVEDGTVTGRRDGDTASEQLQASLPALVSVTDQSGEARYPSFKGIMAAKKKPVESWDLEDLEIEADEVGLEGSWTAVDSAAQRPARTAGTIVKDEGEGGKQLAEFLAGQKFI
>NZ_CP019798.1|WP_030845541.1|1124716_1125679_-|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein
MAEVLVYVDHVDGAVRKPTLELLTLARRIGEPVAVALGAGAEATAAVLAEHGAVKVLTADAPEFADYLVVPKVDALQAAYDAVSPAAVLVPSSAEGKEIAARLAVRIGSGIITDAVDLEAGDEGPVATQSAFAASFTTKSRVSKGTPVITVKPNSAPVEAAPAAGAVEALAVTFGALATGTKVTGRTPRESTGRPELTEAAIVVSGGRGVNGAENFGIIEELADSLGAAVGASRAAVDAGWYPHTNQVGQTGKSVSPQLYIASGISGAIQHRAGMQTSKTIVAINKDAEAPIFDLVDYGVVGDLFTVVPQLTAEIKARKG
>NZ_CP019798.1|WP_060179012.1|1123235_1124534_-|aldolase
MGQQEKVATSLAGAVSEGISASLAPVDAELARHYPGDPGTRQPIHTVYVPGDVFAADTIRSWGDQALAALDEHAPDAATFAKVLGISDELAVPVYDRVRAKLRREPVEDLRVDFEDGFGVRSDEEEDQAAARAARLVSEAFSNGTNAPYMGIRMKCMESNVRDRGIRTTDIFLSGLLEHGGLPEGLVLTLPKVTYAEQVSAFVKLLEAFEATRGLRPGRIGFEIQIETSQSILASDGTATVARMIEAAKGRATGLHYGTFDYSACVGVSAAYQASDHPAADHAKAIMQVAAAGTGVRVSDGSTNVLPIGTTEKVHEGWKLHYGLTRRALARAYYQGWDMHPAHLPTRYAAVFTFYREGLETAAARLKAYVAKIEGDVMDEPATAKALAGYLVRGLDCGAVGADEVTALTGLTRAELDAFAIPRRSATLTATA
>NZ_CP019798.1|WP_060180340.1|1122080_1123118_+|LacI-family-DNA-binding-transcriptional-regulator
MPHNHRPSGPRYGNRPTMKDVAARAGVGLKTVSRVVNGEPGVTPETEKRVQEAIEALGFRRNDSARVLRKGRTATVGLVLEDLADPFYGPLNRAVEEVARAHGALLINGSSAQDPDRERELALALCARRVDGLIVIPAGNDHRYLEPEMRAGVATVFVDRPAGGIDADVVLSDNYGGARGGVAHLVAGGHRRVGFIGDHPRIHTATERLRGYRAAMAEAGLAVAESWVSLGSTEPGRVAAAARSMLAGREPVTAVFAGNNRVTVTVVRVLASLQRPVALVGFDDFELADLLRPGVTVVAQDPAALGRVATDRLFQRLSGTNLPPTRIELPTRLVPRGSGELPPAD
>NZ_CP019798.1|WP_078093646.1|1120896_1121934_-|NUDIX-domain-containing-protein
MIVWINGTFSAGKTSTARELTAILPDSTLFDPEFVGDALRVLLPPKRLAEVTDYQDLPSWRRLVVDTAAAVLAEAGGMLVVPMTLLRQEYRDEIFGGLAARRIPVRHVLLAPAETILRERIATRTEPGAPEDVDLRVRQWAYDHIPAYQEALGWLTGDAHVIDNGLLTVRETAERIAEAVRSDTARVCDIVQTPEPTRETVAAGVLLFDEQDRVLLVDPTYKAGWEFPGGVVEAGEAPARAGVREVAEELGLVLDETPGLLVVDWERPQHPGYGGLRLLFDGGRLSAEAAARLRLPGPELRAWRFVTEAEAAELLPQHRYERLCWALRARERARPLYLEAGVPTG
>NZ_CP019798.1|WP_060180337.1|1118635_1120000_+|dipeptidase
MSQNPIAETVASLMPRAKQELSELVAFQSVADWAQFPKSESEAAANWVADALRAEGFQDVALLDTPDGTQSVYGFLPGPDGAPTVLLYAHYDVQPPLDDDAWISPAFELTERDGRWYGRGAADCKGGFIMHLLALRALKANGGVPVSVKVIVEGSEEQGTGGLQSYAEAHPELLAADTIVIGDAGNFRLGLPTVTATLRGMCLLKLKIDTLGGNLHSGVFGGAAPDALAALIRVLDSLRAADGSTTVDGLAADAVWEGLQYPEADFRSDAKVLDGVELIGAGTIADRLWARPAVTVLGIDCPPVVGATPSVHASAGALISLRVPPGVDTTEAVKLLQAHLEAHTPWKARLELELVGQGQPFRADTDSPAYASMRTALEAAYPGQEMQITGMGGSIPLCNTLTSLYPQAEMLLIGLSEPEAQIHAVNESVSPEELERLSVAEALFLVNYAASKAA
>NZ_CP019798.1|WP_107499845.1|1117093_1118299_-|geranylgeranyl-reductase-family-protein
MWDVVVVGAGPAGSSAAYAAATAGRRVLLLEKAELPRYKTCGGGIIGPSRDALPPGFVLPLKDRIHAVTFSMDGKLTRTRRSKHMLFGLINRPEFDAGLVAEAEKAGATVRTGTAVSRVEQHGAAVPDRRTVAVVLADGETVLARAVVGADGSASRIGAHVGVEMDQVDLGLEAEIPVPATVAEDWKGRVLIDWGPLPGSYGWVFPKGDTLTVGVISAKGEGAATKRYLDDFIARLGLAGFEPAVSSGHLTRCRKPDSPLSRGRVLVAGDAAGLLEPWTREGISFALRSGRLAGEWAVKIAEAQDAVDARRQALNYAFAVKAGLGVEMGVGKRMLTVFEARPGLLHAAITGFRPAWRAFARITRGATTLADMVRTYPLARKALHVLDARQAAAAARTGDGA
>NZ_CP019798.1|WP_078096101.1|1129502_1130102_-|transglutaminase-family-protein
MQLIQQDPDPLAYLASGEAIDHGHPRVQEAADALWFTTGDAYSYAEAAFEFVRDTIPHSADSGDARVAWRASDVLATRNGICHAKSHALVALLRARRIPAGLCYQRLADDDGSNPLVHGLIALRLPGGDRWSRLDPRGNKPGVDARFDLVEERLAFPVRPELGETDYPGLYAAPHPAVLAALRGSADRQELWRRLPTQL
>NZ_CP019798.1|WP_030845522.1|1130186_1131248_-|threonine-aldolase
MKTDARRHHDPAVRGFASDNYAGVHPEILEALALANGGHQVAYGEDEYTEYLQKIIRSHFGPYAEAFPVFNGTGANVTALQAMTDRWGAVICAKSAHINVDEGGAPERMAGLKLLAVPTPDGKLTPELIDQEAWGFEDEHRAMPQVVSITQNTELGTVYTPDEIRAICEHAHGLGMKVHLDGARIANAAASLDVPMRTFTNTVGVDVLSYGGTKNGMMFGEAIVVLNPDAARQMKHIRKMSMQLASKMRFVSVQLEALLAKDLWLRNARHANDMAQRLAAGVRETDGVEILYPVQANAVFARLPHEVSRRLQKRYRFYFWDEAAGDVRWMCGFDTQEEDVDGFLQALKEELAR
>NZ_CP019798.1|WP_030845519.1|1131244_1132006_-|SDR-family-NAD(P)-dependent-oxidoreductase
MNGSGNGNGKLHGAVVAVAGAGGPAGRAALLRLAEAGAVVVASDADPARLAEAVDAARYAHGGATITGDTVDLLDLDATKAWAEQTEKEFGRVDGLVHLVGGWRGSKTFTDVDLADWAFLEKLLIRTVQHTSLAFHDGLLRSDRGRYVLVSQSGAHKPVANNAAYNAGKAAAEAWTLAMADSFRKAGGDEGPGAAAAILVIKALVHDAMRAERPNAKFAGFTDVKELAEAIAGVWERPAIDVNGQRLWLTPQP
>NZ_CP019798.1|WP_030845517.1|1132032_1133439_-|hypothetical-protein
MTETLVPGVGGAVISAGARVVDHPAWLELKAAVEEIRPWQAADGSIDFEAEGEHARATVLAAVERVIGAVEVLSPLLPHATAYHQALIADLRKWAADDFRVPDFLDSLMAFHPAAERADGLQHLVVFPMYTQNGNPDRNLEAVVLKMVWPEWLSELERTRYDNPLFLGITFEDFTPGYDTHSAVLFPETIAVREAPERFTWGGIFCDREAARYRKVTAAAVDILGIDLPEDIARMVDDQERCEKAFVLWDMVHDRTHSHGDLPFDPFMIKQRQPFWMYGLEELRCDLTAFKEAVKLESEGNEHGRDVQYAVLFDRMFRFPVSGDRNRNYDGLGGQLLFAYLHKHDVVRWTDNKLKIDWMRAPQVTNQLCAEIEDLYRAGIDRPKLVHWFKAYELVSTYLAPHPGSKWAKGADALDLTQPPRKLVDDVLPDEFPLSMFFEALAKKLKGTIASTKGITALNAEHAERVAA
>NZ_CP019798.1|WP_078093650.1|1133520_1134543_-|alpha/beta-hydrolase
MAARRESRPATDRDRLDPAALPWVDALTASFPDLGRTVTSADEARRILAAAPRPAAVPPAVGSVEDRTVPGPPGAPPVPVRIYRPDPERWPGPRPTVVFCHGGGWVLCDLDTHDGTARRIVRAAGAALVSVDYRRAPEHRFPAAVEDAHAALCWAGDHLDDLGGDPGALVVAGDSSGGNLAAASLLLARERGGPAVALQALIHPALDAARERASYRSAAEGCFLTAGHMRWFWEQYLGPGGDGRHPLASPLRADPAGLPPAHLVLAGCDPLRDDGHAYHHRLRRSGIRSVLDSHPGMFHGFLGLAGLLPQACEALARLGGAISSTLTDGKTFGEAGGDAG
>NZ_CP019798.1|WP_078093651.1|1134542_1135664_-|LLM-class-flavin-dependent-oxidoreductase
MKFSVIFEAQLADPTVEREHRLIHDCVEQAVFAERMGFDRIWAVEHHSLKWYAHMSAPEVFLSWIAARTRTIRIGHGVVCMPFNFNHPVRVAERAAMLDLLSGGRLDLGAGRGGTEQETSLCGVDKERTTAEVEEALRIIGRAWQEEELEYHGELIDIDPHPILPRPRQTPHPPLFLACSRGETLVQAAELGIGALVMGFAGPDSIAQMRSVYDAAIAGRDGSRFVSTAVNDHFSVLCPTIVLDDGERARRIGIRGQRFFAQSIGHWYGGAGVPDEAVVAGADEAGEMRRAAEQVVARLHELDIPVRPTSTATFNADHAYGTADDAIAYVARLREAGADEVMCLIQMGTVEQEICMETLRQWGEKVIPHFRSR
>NZ_CP019798.1|WP_173675202.1|1135713_1136340_+|PadR-family-transcriptional-regulator
MTSSHKSKKQDLPPTAWAVLGLLSFPGERTGYELKKWADSSLRFFYWSPAISQIYAELRRLEELGYASSARSGPEEVRAKRRYAITEAGREALAHWAADTTEAGPPVLKHGLLLRVWLGHLAEPARLRAMVGEHLERTREELDAVREAAQEAAGVREWAFPAVALRWSERQHLAELELAEALLADLAQLAPPDGTAGRQAGGDAPTPG
>NZ_CP019798.1|WP_030845504.1|1136532_1137225_+|glycerophosphodiester-phosphodiesterase
MTFLTIGHRGVMGVEPENTLRSYLRAERSGMDAIALDLRLSKDGVLVAVHDPEVDRTTDGSGAVADLTLAELRGLDAGQGERVPVFEEVLEAVRSPLHVSVQDRPAAVALAELLLRRDLVSRVEIASAHESVLTEAARRVPGVRTTLSVSSPGGDTGALVGRALAAGAATIALDIHHIALETVEAAHTAGLRITALAVNTLDQLRLARALGLDGVATDFPEIRSTGRFTA
>NZ_CP019798.1|WP_030845502.1|1137246_1137792_-|GNAT-family-N-acetyltransferase
MSTAQPAALSFRSAVEADVPELVALVESAYRGDASRAGWTTEADYLDGQRTDPDGVRAVIDAEDGDLLVVERAGELVACCHIEHRGDHAYFGMFAVRPGLQGAGLGREILAEAERRARETWGAGEMRMTVVNVREELIAYYVRRGYRRTGELSPFPYGDERFGIPLRDDLAFELLVKPLQP
>NZ_CP019798.1|WP_078093653.1|1137818_1138481_+|DUF5134-domain-containing-protein
MTCRGRQGEPIPGPSEGRVRRASLWRDADEPGGSAVHGSASPLSASAWLLVLLGAVSGAYCLRRARGWGGAAAGEAVMGFGMALMAVPLGDGGAWRAPVLGAVFCVAAVHALWLLRGGAHHAHHLVGSLTMVYMVYGAAAAGSGGQGHGHGTGLPLLTGALLLYYAGYVVLGGTRLITAGGAAPAPSPASPAPPCGAPAELARACRLAMGMGMLAMLPAM

Crispr_ID: NZ_CP019798_3

• CRISPR_ID: NZ_CP019798_3
• CRISPR_location: 2068166-2068323
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP019798_3

Consensus_repeat	Method
GCCGCCGCCGGAGCCGCCGC	CRT

spacers of NZ_CP019798_3

>3.1|2068186|28|NZ_CP019798|CRT
GGTAGCCGCCGCCACCGCCGGAGCCGGA
>3.2|2068234|31|NZ_CP019798|CRT
CGCTGCCCGAGCCGGAGCCGCGGTAGCCACC
>3.3|2068285|19|NZ_CP019798|CRT
CACGGGCGCTACCGCGCCC

CRISPR arrays and Neighbor proteins around NZ_CP019798_3

CRISPR arrays

The CRISPR arrays of NZ_CP019798_3

>merge|NZ_CP019798|3|2068166-2068323|CRT
GCCGCCGCCGGCACCGCCCCGGTAGCCGCCGCCACCGCCGGAGCCGGAGCCGCCGCGGTAGCCGCCGCCGCTGCCCGAGCCGGAGCCGCGGTAGCCACCGCCGCCGCCGGAGCCGCCGCCACGGGCGCTACCGCGCCCGCCGCCGCCGGAGCCGCCGC

>NZ_CP019798|3|2|2068166-2068323|CRT
GCCGCCGCCGGCACCGCCCC	GGTAGCCGCCGCCACCGCCGGAGCCGGA
GCCGCCGCGGTAGCCGCCGC	CGCTGCCCGAGCCGGAGCCGCGGTAGCCACC
GCCGCCGCCGGAGCCGCCGC	CACGGGCGCTACCGCGCCC
GCCGCCGCCGGAGCCGCCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_060179950.1|2081013_2082399_+|FAD-binding-oxidoreductase	unknown	unknown	gnl|CDD|223354
NZ_CP019798.1|WP_030855306.1|2059532_2060240_-|(d)CMP-kinase	unknown	unknown	gnl|CDD|234579
NZ_CP019798.1|WP_030855330.1|2079092_2080904_+|glycoside-hydrolase-family-15-protein	unknown	unknown	gnl|CDD|225922
NZ_CP019798.1|WP_076044055.1|2070736_2071276_-|hypothetical-protein	unknown	unknown	gnl|CDD|237171
NZ_CP019798.1|WP_078093949.1|2063495_2064506_-|ADP-ribosylglycohydrolase-family-protein	unknown	unknown	gnl|CDD|377122
NZ_CP019798.1|WP_060179962.1|2061795_2062137_+|DUF952-domain-containing-protein	unknown	unknown	gnl|CDD|377607
NZ_CP019798.1|WP_078093952.1|2074016_2076041_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|276809
NZ_CP019798.1|WP_030855320.1|2068362_2068995_-|SMC-Scp-complex-subunit-ScpB	unknown	unknown	gnl|CDD|377219
NZ_CP019798.1|WP_107499859.1|2068991_2070068_-|segregation/condensation-protein-A	unknown	unknown	gnl|CDD|280735
NZ_CP019798.1|WP_060179951.1|2076975_2078628_-|CTP-synthase	unknown	unknown	gnl|CDD|235437
NZ_CP019798.1|WP_030855327.1|2076261_2076894_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|239516
NZ_CP019798.1|WP_078093948.1|2062219_2062702_+|Rieske-(2Fe-2S)-protein	unknown	unknown	gnl|CDD|239550
NZ_CP019798.1|WP_076044056.1|2071260_2072421_-|ParA-family-protein	unknown	unknown	gnl|CDD|379293
NZ_CP019798.1|WP_060179957.1|2065239_2066319_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|273670
NZ_CP019798.1|WP_159425522.1|2061561_2061720_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030855324.1|2072747_2073863_-|alanine-dehydrogenase	unknown	unknown	gnl|CDD|240630
NZ_CP019798.1|WP_060179958.1|2064502_2065243_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|223979
NZ_CP019798.1|WP_030855312.1|2062775_2063459_+|nucleotidyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|313370
NZ_CP019798.1|WP_060179963.1|2060357_2061446_-|prephenate-dehydrogenase	unknown	unknown	gnl|CDD|235824
NZ_CP019798.1|WP_060179956.1|2066315_2066924_-|nicotinamide-mononucleotide-transporter	unknown	unknown	gnl|CDD|377432

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_060179950.1|2081013_2082399_+|FAD-binding-oxidoreductase	gnl|CDD|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	5.71408e-44
NZ_CP019798.1|WP_030855306.1|2059532_2060240_-|(d)CMP-kinase	gnl|CDD|234579	PRK00023, cmk, (d)CMP kinase.	3.40308e-96
NZ_CP019798.1|WP_030855330.1|2079092_2080904_+|glycoside-hydrolase-family-15-protein	gnl|CDD|225922	COG3387, SGA1, Glucoamylase and related glycosyl hydrolases [Carbohydrate transport and metabolism].	9.15469e-141
NZ_CP019798.1|WP_076044055.1|2070736_2071276_-|hypothetical-protein	gnl|CDD|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	0.000399042
NZ_CP019798.1|WP_078093949.1|2063495_2064506_-|ADP-ribosylglycohydrolase-family-protein	gnl|CDD|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	4.41877e-37
NZ_CP019798.1|WP_060179962.1|2061795_2062137_+|DUF952-domain-containing-protein	gnl|CDD|377607	pfam06108, DUF952, Protein of unknown function (DUF952). This family consists of several hypothetical bacterial and plant proteins of unknown function.	1.92413e-21
NZ_CP019798.1|WP_078093952.1|2074016_2076041_-|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.	2.02838e-05
NZ_CP019798.1|WP_030855320.1|2068362_2068995_-|SMC-Scp-complex-subunit-ScpB	gnl|CDD|377219	pfam04079, SMC_ScpB, Segregation and condensation complex subunit ScpB. This is a family of prokaryotic proteins that form one of the subunits, ScpB, of the segregation and condensation complex, condensin, that plays a key role in the maintenance of the chromosome. In prokaryotes the complex consists of three proteins, SMC, ScpA (kleisin) and ScpB. ScpB dimerizes and binds to ScpA. As originally predicted, ScpB is structurally a winged-helix at both its N- and C-terminal halves. IN Bacillus subtilis,one Smc dimer is bridged by a single ScpAB to generate asymmetric tripartite rings analogous to eukaryotic SMC complex ring-shaped assemblies.	5.07238e-65
NZ_CP019798.1|WP_107499859.1|2068991_2070068_-|segregation/condensation-protein-A	gnl|CDD|280735	pfam02616, SMC_ScpA, Segregation and condensation protein ScpA. This is a family of proteins that from part of the condensin complex that regulates chromosome segregation. This is the A subunit, which binds to the ScpB subunit, pfam04079, and SMC, pfam02463, to participate in chromosomal partition during cell division. The condensin complex pulls DNA away from the mid-cell into both cell halves. These proteins are part of the Kleisin superfamily.	2.6964e-54
NZ_CP019798.1|WP_060179951.1|2076975_2078628_-|CTP-synthase	gnl|CDD|235437	PRK05380, pyrG, CTP synthetase; Validated.	0
NZ_CP019798.1|WP_078093948.1|2062219_2062702_+|Rieske-(2Fe-2S)-protein	gnl|CDD|239550	cd03467, Rieske, Rieske domain; a [2Fe-2S] cluster binding domain commonly found in Rieske non-heme iron oxygenase (RO) systems such as naphthalene and biphenyl dioxygenases, as well as in plant/cyanobacterial chloroplast b6f and mitochondrial cytochrome bc(1) complexes. The Rieske domain can be divided into two subdomains, with an incomplete six-stranded, antiparallel beta-barrel at one end, and an iron-sulfur cluster binding subdomain at the other. The Rieske iron-sulfur center contains a [2Fe-2S] cluster, which is involved in electron transfer, and is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In RO systems, the N-terminal Rieske domain of the alpha subunit acts as an electron shuttle that accepts electrons from a reductase or ferredoxin component and transfers them to the mononuclear iron in the alpha subunit C-terminal domain to be used for catalysis.	5.44291e-20
NZ_CP019798.1|WP_076044056.1|2071260_2072421_-|ParA-family-protein	gnl|CDD|379293	pfam13614, AAA_31, AAA domain. This family includes a wide variety of AAA domains including some that have lost essential nucleotide binding residues in the P-loop.	4.02142e-87
NZ_CP019798.1|WP_060179957.1|2065239_2066319_-|AAA-family-ATPase	gnl|CDD|273670	TIGR01526, nadR_NMN_Atrans, nicotinamide-nucleotide adenylyltransferase, NadR type. The NadR protein of E. coli and closely related bacteria is both enzyme and regulatory protein. The first 60 or so amino acids, N-terminal to the region covered by this model, is a DNA-binding helix-turn-helix domain (pfam01381) responsible for repressing the nadAB genes of NAD de novo biosynthesis. The NadR homologs in Mycobacterium tuberculosis, Haemophilus influenzae, and others appear to lack the repressor domain. NadR has recently been shown to act as an enzyme of the salvage pathway of NAD biosynthesis, nicotinamide-nucleotide adenylyltransferase; members of this family are presumed to share this activity. E. coli NadR has also been found to regulate the import of its substrate, nicotinamide ribonucleotide, but it is not known if the other members of this model share that activity.	1.81274e-57
NZ_CP019798.1|WP_030855327.1|2076261_2076894_-|NUDIX-hydrolase	gnl|CDD|239516	cd03424, ADPRase_NUDT5, ADP-ribose pyrophosphatase (ADPRase) catalyzes the hydrolysis of ADP-ribose and a variety of additional ADP-sugar conjugates to AMP and ribose-5-phosphate. Like other members of the Nudix hydrolase superfamily, it requires a divalent cation, such as Mg2+, for its activity. It also contains a highly conserved 23-residue Nudix motif (GX5EX7REUXEEXGU, where U = I, L or V) which functions as a metal binding site/catalytic site. In addition to the Nudix motif, there are additional conserved amino acid residues, distal from the signature sequence, that correlate with substrate specificity. In humans, there are four distinct ADPRase activities, three putative cytosolic enzymes (ADPRase-I, -II, and -Mn) and a single mitochondrial enzyme (ADPRase-m). Human ADPRase-II is also referred to as NUDT5. It lacks the N-terminal target sequence unique to mitochondrial ADPRase. The different cytosolic types are distinguished by their specificities for substrate and specific requirement for metal ions. NUDT5 forms a homodimer.	3.39867e-40
NZ_CP019798.1|WP_030855324.1|2072747_2073863_-|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_CP019798.1|WP_060179958.1|2064502_2065243_-|NUDIX-hydrolase	gnl|CDD|223979	COG1051, COG1051, ADP-ribose pyrophosphatase [Nucleotide transport and metabolism].	6.15582e-29
NZ_CP019798.1|WP_030855312.1|2062775_2063459_+|nucleotidyltransferase-domain-containing-protein	gnl|CDD|313370	pfam10127, Nuc-transf, Predicted nucleotidyltransferase. Members of this family of bacterial proteins catalyze the transfer of nucleotide residues from nucleoside diphosphates or triphosphates into dimer or polymer forms.	5.0914e-37
NZ_CP019798.1|WP_060179963.1|2060357_2061446_-|prephenate-dehydrogenase	gnl|CDD|235824	PRK06545, PRK06545, prephenate dehydrogenase; Validated.	6.29838e-126
NZ_CP019798.1|WP_060179956.1|2066315_2066924_-|nicotinamide-mononucleotide-transporter	gnl|CDD|377432	pfam04973, NMN_transporter, Nicotinamide mononucleotide transporter. Members of this family are integral membrane proteins that are involved in transport of nicotinamide mononucleotide.	1.883e-55

Protein sequences

>NZ_CP019798.1|WP_060179956.1|2066315_2066924_-|nicotinamide-mononucleotide-transporter
MNWTLSWTEVLGFATGALCVWLVARQHIANWPIGIANNVFFIVLFAQAGLYADAGLQIVFIALAAYGWWSWTHGGGPGTAAALPVRRTTRTEWVWLAAAGAAGTLGLTLLLARATDSTVPVWDAATTALSLAATYGQCRKLVESWWLWIAADLLYIPLYVHKGLHLTALLYVGFLALCVAGLLGWRRSLPQRGARTALEATA
>NZ_CP019798.1|WP_060179957.1|2065239_2066319_-|AAA-family-ATPase
MRRFGHGLVLGKFYPPHAGHHHLVRTAQDRCERLTVLVCAASVESVPLADRVAWMREAHPDADVVGAVDDIPVDLHDPEIWEAHMAIFRAAVGRRVDAVFTSEEYGTELARRFGAEEVCVDPARTLFPVSGTAVRADPAACWDFLGPAVRARLARRVVVLGAESTGTTTLSRDLAAHLRARGGVWAATGWVEEYGRRYSEEKLAAARAADPAATWADVSFTSEEFPVIARRQDEEEERAARQGSPVLVCDTDSFATGIWHERYMGGRNPEVERIAALTHRDLYLLTEDADVPFEDDGLRDGPELRPWMTRRFREELEATGKRYLSVRGNRRERLATAAAAVDELLAEGWRFADPLPENR
>NZ_CP019798.1|WP_060179958.1|2064502_2065243_-|NUDIX-hydrolase
MSGAVDPGYDPHAFEPFAVTVDLAVFTVRGGALHVLLIRRGQEPYAGSWALPGGFVLPRESAETAARRELAEETGLPEQVVAALHLEQLRTYSEPDRDPRMRVVSVAFTALVPDLPEPAAEGGGDAAQARWLPLGEVPDLAFDHAVILADARMRIRSKLEYTCLATAFCPPEFTLGELLAVYETVWDTVLDRPNFRRKVLTTPGFVEAVPGAARLTGGRGKPAALYRAGPATALHPPLLRPEGPTP
>NZ_CP019798.1|WP_078093949.1|2063495_2064506_-|ADP-ribosylglycohydrolase-family-protein
MTKRAATGALVGLALGDALGFPTEFNDVPAILAKTGPWREMRLPRPAIVTDDTQMTLALARGIRTATDRGPIGPLRLTRPVREEFVDWYHSPENNRAPGNTCLRACNLLNDPQRDWRDASQTGSKGCGANMRVVPVGLVPGWTDEERAGAAQLQSALTHGHPTALAASDLTALAVHLLATGTEVTGLVGRLRSYALENRTRYHERWLGDLWMRTASDATPESFIARGWDECLEVLDRLAAALKTPSPETDPCLTTGDGWIAEEALATALQCFLLFPDEPLTALRRAACTRGDSDSLACLAGAFAGAHLGADVWPREWEGRIEYRDELLAFGTLWDA
>NZ_CP019798.1|WP_030855312.1|2062775_2063459_+|nucleotidyltransferase-domain-containing-protein
MDDLTLVREHTVYRCVMGSRAFGLATEASDTDRRGVYLAPTPLFWRFEKPPTHVDGPRDEEFSWELERFCELALRANPNILECLHSPLVEHVSAVGAELLSLRGAFLSRRAHTSFGRYAASQHGKLVADVRLHGAPRWKHAMHLLRLLLSCRDLLRTGHLAIDAGPYRDRLLAVRRGELTWDEVDTWMTRLQEETEDALAGTPLPEEPDRARVEDFLVRARRASALQ
>NZ_CP019798.1|WP_078093948.1|2062219_2062702_+|Rieske-(2Fe-2S)-protein
MSDPTQTARRKVLVIGAATLAGGALTACGSGGDGGNTASAEPNGAASPPPGDRPANPSAGGAPAGKAIAKAADVPVGGGKVLKEQKVVVTQPTAGSFRCFTAVCPHQGCLVTKVENNAINCACHNSEFKATDGAVVKGPATKGLAEKKITVAADGNITLA
>NZ_CP019798.1|WP_060179962.1|2061795_2062137_+|DUF952-domain-containing-protein
MIFHIVPLADWTASPELPYAPPSLDSEGFVHCSADRATVLGIADTHYRAQPGTLLAVELDEDALTAEVRREGDSGDRFPHVFGPLNRDAVVHVWEVVRTPGTPASLAPWQRSS
>NZ_CP019798.1|WP_159425522.1|2061561_2061720_-|hypothetical-protein
MSPSRTALSARPGPEQAADRIAQSLPRAVDRLTPGGVIPSGPIEDIIRQQKS
>NZ_CP019798.1|WP_060179963.1|2060357_2061446_-|prephenate-dehydrogenase
MRTAVVIGTGLIGTSAALALTARGITVHLADHDPDRARTAAALGAGTDEPPQEQVDLAIVAVPPAHVAATLADLIGRGAARAYVDVASVKGGPRRELAALGVDATAYIGTHPMAGKEQSGPLAATADLFEGRPWVLTPTRDTDHEVLNLALELVALARAVPVVMDADAHDRAVALVSHTPQLVSSMVAARLEEADETAVRLCGQGIRDVTRIAASDPRMWVEILSANPGPVADVLAGIAADLEETVDALRSLQSADVDKRRGGAAGIEDVLRRGNAGRVRVPGKHGAAPTVYETVAVLISDQPGELARIFADAGRAGVNIEDVRIEHATGQQAGLVQLMVEPRSAAGLTAELRERGWALRTS
>NZ_CP019798.1|WP_030855306.1|2059532_2060240_-|(d)CMP-kinase
METAAPSAVIVAIDGPSGTGKSSTSKAVAAKLGLRYLDTGAQYRAITWWMISNGVDTDDAQAVAVAAGKPSIVSGTDPAAPTITVDGLDAAGPIRTQEVTSKVSAVSAVPEVRTLITELQRSIAAEAARDADGIVVEGRDIGTTVLPDADLKIFLTASAEARAARRSGELRGKEAADLAATKAALIKRDAADSGRKTSPLAKAGDAVEVDTTELTLDQVIECVVTLVEEKRAGRR
>NZ_CP019798.1|WP_030855320.1|2068362_2068995_-|SMC-Scp-complex-subunit-ScpB
MSGDGGAVAALELKPALEAVLMVVDEPATEAHLAKVLERTPREVADALRELADEYTAARRGFELRLVAGGWRFYTRAQYAPAVEAFVLDGQQARLTQAALETLAVVAYRQPVSRSRVSAVRGVNCDGVMRTLLQRGLVEEAGTEPETGAILYRTTNYFLERMGLRGLDELPELAPFLPEADAIEAETQEGVPSFDPDAPDTDEDDKTTEL
>NZ_CP019798.1|WP_107499859.1|2068991_2070068_-|segregation/condensation-protein-A
MPPDHHAARPARRSLGRGPGAAAEAPVSEPAAAEAPATGPEAAESAGAVGGPGGPAAETGDPAGPADGAGAADAAGRAEGAGPGQGGSATAPGGDGRFTLRLDNFEGPFDLLLQLISRHKLDITEVALSKVTDEFMAHIRAMGPDWDLDQTTEFLVVAATLLDLKAARLLPVAEVEDEADLALLEARDLLFARLLQYRAYKQIAEIFERRAQSEGRRYPRTVGLEPHHADLLPDVVISIGAEGFARLAVKAMQPKAKPEVYVDHIHAPLVSVREQAGVVVRMLKARGEATFQELTEDAEDTLTVVARFLALLELYREKAVALDQEEALRTLTVRWSGGDGDGMPTVTDEFDQIVEAKD
>NZ_CP019798.1|WP_076044055.1|2070736_2071276_-|hypothetical-protein
MSRRVSLPGADELFRTTGGMALQSSSPRRGADEASAAEHSAAPAGGTAGEGRSREAEAGTQADGPVVGQPRRPQEGSVSQAGPAAGAASAPAGATRRGKGQGRGANRRPSGRERHDEKITVYVSAEELMDLEHARLVLRGEHGLAVDRGRIVREAVAVVLADLESRGDASILVRRLRGR
>NZ_CP019798.1|WP_076044056.1|2071260_2072421_-|ParA-family-protein
MNKSTFTPGGGGAGVPERGQSPAGLEAVGSVAVRTFANHQHMTTPQKSMDGLDVNSRAGDLSGDTPTGFADYDNVPEGHFYDPDAEYEPDPEYAATLAPDAARQRRERIGPTGRPLPYFPIPGPLTDHGPAKIIAMCNQKGGVGKTTSTINLGAALAEYGRRVLLVDFDPQGALSVGLGVNPMELDLTVYNLLMERGMSADEVLLKTAVPNMDLLPSNIDLSAAEVQLVSEVARESTLQRALKPLMADYDYIVIDCQPSLGLLTVNALTAAHKVIVPLECEFFALRGVALLTETIEKVQERLNPELELDGILATMYDSRTVHSREVLARVVEAFDDHVYHTVIGRTVRFPETTVAGEPITTYASNSVGAAAYRQLAREVLARCHAE
>NZ_CP019798.1|WP_030855324.1|2072747_2073863_-|alanine-dehydrogenase
MKVGIPREVKNNEFRVAITPAGVHELVRNGHQVFIEQNAGVGSSITDAEYVAAGAEILGTADEVWATADLLLKVKEPIAEEYHRLRKDQTLFTYLHLAASRECTDALLESGTTAIAYETVELANRALPLLAPMSEVAGRLAPQVGAYHLMRSAGGRGVLPGGVPGTHAGECVVIGGGVSGWNAAQIAIGMGFHVTLLDRDINKLREADKIFGTKIKTIVSNAYELEKAVVEADLVIGAVLIPGAKAPKLVTNELVAKMKPGSVLVDIAIDQGGCFEDSRPTTHAEPTFQVHNSVFYCVANMPGAVPNTSTYALTNATLPYIVQLANLGWVEALRRDPALALGLNTHDGQVVYGPVAEAHGLETLELGTLLG
>NZ_CP019798.1|WP_078093952.1|2074016_2076041_-|tetratricopeptide-repeat-protein
MRELRSPSEGSERSGSVTDFVGRRRELKELREDIARTGLDTLSGRKAKAPRARVLLVAGRPGSGRTALAETFVREIADQYPDGVLRTRLTAPGGETVATERALRGLLAGLGRSTPPGAGEDELSSVLRTALQERKAIILIDDAADPHQVDALLPDTPECLVVVTAEGPLTGIPDVRPCTLGGLDTASAVGMLARRIGDTRITADPRAAESLAEACGGQPAALELAGGWLAARPKAAVADVAKKLHDMPAGAGGPLGRAFRLVYDSLPQPAQRTLRLLPLAPAGLVDSHTASALAGCSVAAAQSTLDDFAGLGLVRHAPDGLFLLPGSLAPMLQALLEAKERPAEVQLARARMLERTVRLLHSCRAMAAAEGDDPDSELQELLDGLPRALRFPDRRAAALWLDTRLPALTAAASLAVADGELDTLARRLVAALVRALADHRGTAEAAPELYGLHRLVLDVAERRGLHREQAAALLNLADLDAETGRTQEALERYRAALDAGRAANDPYATGRAMESVGGAYQELADWHRASDWFGRALAQALSRGERADEARLYGRLGNVHTYAGRYGDALRSWRAAAAGYRKLADVPGQAKALSEMARIQEYAGRPEESLHTCREAVELARRAGDQRLQAALQVRLADTLDRLGDPAAARLHRSAADRLLGDDPAACEIRSGSD
>NZ_CP019798.1|WP_030855327.1|2076261_2076894_-|NUDIX-hydrolase
MNIKDTAESWETLSTRRPFQGAKTAVDSDEVRMPDGSTARRDYQVHPGSVCVLALDGEGRVLVLSQYRHPVRRRLWELPAGLLDVPGENPLLGAQRELYEEAHAKAEDWRVLVDFYASPGGSDEAIRVFLARGVSEADGERYRESDSEEADMEVAWVPLAELVQGILAGELGNPGLVTGVLALSAALAREGGVDALRPALAPWPARPYEA
>NZ_CP019798.1|WP_060179951.1|2076975_2078628_-|CTP-synthase
MPPKSMTTKHIFVTGGVASSLGKGLTASSLGALLKARGLRVTMQKLDPYLNVDPGTMNPFQHGEVFVTNDGAETDLDIGHYERFLDVDLDGSANVTTGQVYNTVIAKERRGEYLGDTVQVIPHITNEIKHRIRRMATDDVDVVITEVGGTVGDIESLPFLETVRQVRHEVGRDNVFVVHISLLPYIGPSGELKTKPTQHSVAALRNIGIQPDAIVLRADRDVPTSIKRKISLMCDVDEAAVVAAIDAKSIYDIPKVLHTEGLDAYVVRKLDLPFRDVDWTVWEDLLDRVHNPDHEVKVALVGKYIDLPDAYLSVTEALRAGGFANKARVQIKWVTSDDCKTPAGAAAQLSDVDAICVPGGFGDRGVNGKVGAITYARENKIPLLGLCLGLQCVVIEAARNLAGIDDANSTEFDASTPHPVISTMEEQLAFVEGAGDLGGTMRLGMYPAKLAEGSIVREVYGDQAYVDERHRHRYEVNNAYRSELEKKAGIVFSGTSPDNKLVEYVEYPREVHPYLVATQAHPELRSRPTRPHPLFAGLVKAAVERQQSAK
>NZ_CP019798.1|WP_030855330.1|2079092_2080904_+|glycoside-hydrolase-family-15-protein
MHVSGRIEDYALIGDMQTAALVCRDGAVDWLCLPRFDSHAVFASILGTEDHGFWRIGPSVPAGSEAPRATRRRYRGDSLVLESEWDTPRGNVRVIDFMPPREDHAPQLIRIVEGVSGRVPMRSTLRMRFSYGRVVPWVHKVDGRTVAVAGPDSVWLDTDAQTYGKDLTTYSDFTVGPGDRVAFSISWQPSHRGAPEAPDAEAALESTAEFWREWVDQCTYHGPYREAVVRSLITLKALTYAPTGGIVAAPTTSLPEEIGGVRNWDYRYTWLRDAAITLSSLLRTGYREEARAWREWLLRAVAGDPENLQIMYGIAGERELGETELDWLPGYEGSRPVRVGNGAAGQLQLDVYGEVTEALHLGHMTGLARSDYASLLQLKLIRYLETHWSEPDEGIWEVRGPRRHFVHSKVMAWVAVDRTIKLIESGDADGPLERWRELRDEIHQDVCEKGYDKERNTFTQSYGSKELDASLLLIPQMGFLPPDDKRVIGTIEAIQRELSTPDGFILRYPTAGEEAGVDGLEGDEGAFLACSFWMADDLAMIGRVDEARRLFERLLALRNDLGLLAEEWDPRLQRQVGNFPQAFSHVPLIDTALRLTASGAYGG
>NZ_CP019798.1|WP_060179950.1|2081013_2082399_+|FAD-binding-oxidoreductase
MAPLSKAGAALAALREDLSGEVFAPQDPGYDEARTVFNAMIDRRPAVIAQCESAEDVATAVRFARDLDLKIAVRGGGHSVSGSALGDGALVIDLRRMHEVTVHPGARAVRVEGGATMSHLDRACAPYGLATTGGRASTTGVGGFVLGGGSGWLDRKCGLAVDNLLGVELVTADGSVVETTSQERPELFWALHGGGGNFGVATAITLRLHELPAMAIAFVLYLPENGPEVVRTYRDLLEDGPAEASGGVIFLTGPPDDDFVPPHLAGRLVCAALLTYAGPEERLRKLAEPLLALPHEAAMVTAIPYADLQCMIDDPPGLRNYWSAEYLTAAPDAFVDVFCARAASMPVPTGTQHILFPQGGAIASGPADYPVPYRDSPWAVHPFGIWEDPADDERCRQWVKDVRADVAPWSTGAVYLNFTGDEGSDRVVSGLGADNMRRLGRVKRQYDPDNVFRFNHNIRPA

Crispr_ID: NZ_CP019798_4

• CRISPR_ID: NZ_CP019798_4
• CRISPR_location: 2096723-2097751
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 13 spacers

Consensus repeat of NZ_CP019798_4

Consensus_repeat	Method
GNTCGCCACCNCGGTCGTCNCGNC	CRT

spacers of NZ_CP019798_4

>4.1|2096747|51|NZ_CP019798|CRT
GCGGGTACGACGGACGGTCGCCACCCCGCTCGTCACGACGCGGGTACGAGG
>4.2|2096822|54|NZ_CP019798|CRT
GCGGGTACGAGGGACGCTCGCCGCCTCGGTCGTCACGGCGCGGGTACGAGGGAC
>4.3|2096900|51|NZ_CP019798|CRT
GGAAGGACGGACGCTCACCACCCCGGTCGTCGCGACGGGGGTACGAGGGGC
>4.4|2096975|45|NZ_CP019798|CRT
CGCCGCGGTATCCCCCACGGTCGTCATCACGACGCGGGTACGACG
>4.5|2097044|54|NZ_CP019798|CRT
GCGGGTACGACGGACGGTCGCCACCACGGTCATCACGGCGCGGGTAGGAGGGGC
>4.6|2097122|48|NZ_CP019798|CRT
CGCCGCGGTATCCACCACGGTCGTCGTCCCGACGCGGGTACGAGGGAC
>4.7|2097194|51|NZ_CP019798|CRT
GCGGGTAGGACGGGCGGTCGCCACCTCGGTCATCACGACGGAAGGACGGAC
>4.8|2097269|54|NZ_CP019798|CRT
GGGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGAGGGGC
>4.9|2097347|48|NZ_CP019798|CRT
CGCCGCGGTATCCACCACGGTCGTCATCACGACGCGGGTACGAGGGAC
>4.10|2097419|51|NZ_CP019798|CRT
GCGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGACGGAAGGACGGAC
>4.11|2097494|54|NZ_CP019798|CRT
GGGGGTACGAGGGGCGGTCGCCGCCACGGTCGTCACGGCGCGGGTAGGAGGGGC
>4.12|2097572|54|NZ_CP019798|CRT
GCGGGTACGAGGGACGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGACGGGC
>4.13|2097650|78|NZ_CP019798|CRT
GGAAGGACGGGCGGTCGCCACCGCCGGCGGGACGCCCACCACGGTCGTCGCGACGGTAGCCACCGCCGCTGCCTGCCG

CRISPR arrays and Neighbor proteins around NZ_CP019798_4

CRISPR arrays

The CRISPR arrays of NZ_CP019798_4

>merge|NZ_CP019798|4|2096723-2097751|CRT
GACGCTCACCCCGGTCGTCGCGACGCGGGTACGACGGACGGTCGCCACCCCGCTCGTCACGACGCGGGTACGAGGGACGCTCACCCCGGTCGTCGCGACGCGGGTACGAGGGACGCTCGCCGCCTCGGTCGTCACGGCGCGGGTACGAGGGACGGTCGCCACCACGGTCGTCACGACGGAAGGACGGACGCTCACCACCCCGGTCGTCGCGACGGGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGGCCGCCGCGGTATCCCCCACGGTCGTCATCACGACGCGGGTACGACGGACGCTCACCCCGGTCGTCACGGCGCGGGTACGACGGACGGTCGCCACCACGGTCATCACGGCGCGGGTAGGAGGGGCGGTCGCCACCACGGTCGTCACGGCCGCCGCGGTATCCACCACGGTCGTCGTCCCGACGCGGGTACGAGGGACGCTCGCCGCCCCGGTCATCGCGGCGCGGGTAGGACGGGCGGTCGCCACCTCGGTCATCACGACGGAAGGACGGACGGTCGCCGCCACGGTCGTCACGACGGGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGAGGGGCGGTCGCCACCACGGTCGTCACGCCCGCCGCGGTATCCACCACGGTCGTCATCACGACGCGGGTACGAGGGACGCTCGCCGCCACGGTCATCGCGGCGCGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGACGGAAGGACGGACGGTCGCCGCCACGGTCGTCACGACGGGGGTACGAGGGGCGGTCGCCGCCACGGTCGTCACGGCGCGGGTAGGAGGGGCGGTCGCCACCACGGTCATCGCGGCGCGGGTACGAGGGACGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGACGGGCGGTCGCCACCACGGTCATCACGACGGAAGGACGGGCGGTCGCCACCGCCGGCGGGACGCCCACCACGGTCGTCGCGACGGTAGCCACCGCCGCTGCCTGCCGGGCGGCCACCGCGGTCGTCACGGC

>NZ_CP019798|4|3|2096723-2097751|CRT
GACGCTCACCCCGGTCGTCGCGAC	GCGGGTACGACGGACGGTCGCCACCCCGCTCGTCACGACGCGGGTACGAGG
GACGCTCACCCCGGTCGTCGCGAC	GCGGGTACGAGGGACGCTCGCCGCCTCGGTCGTCACGGCGCGGGTACGAGGGAC
GGTCGCCACCACGGTCGTCACGAC	GGAAGGACGGACGCTCACCACCCCGGTCGTCGCGACGGGGGTACGAGGGGC
GGTCGCCACCACGGTCGTCACGGC	CGCCGCGGTATCCCCCACGGTCGTCATCACGACGCGGGTACGACG
GACGCTCACCCCGGTCGTCACGGC	GCGGGTACGACGGACGGTCGCCACCACGGTCATCACGGCGCGGGTAGGAGGGGC
GGTCGCCACCACGGTCGTCACGGC	CGCCGCGGTATCCACCACGGTCGTCGTCCCGACGCGGGTACGAGGGAC
GCTCGCCGCCCCGGTCATCGCGGC	GCGGGTAGGACGGGCGGTCGCCACCTCGGTCATCACGACGGAAGGACGGAC
GGTCGCCGCCACGGTCGTCACGAC	GGGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGAGGGGC
GGTCGCCACCACGGTCGTCACGCC	CGCCGCGGTATCCACCACGGTCGTCATCACGACGCGGGTACGAGGGAC
GCTCGCCGCCACGGTCATCGCGGC	GCGGGTACGAGGGGCGGTCGCCACCACGGTCGTCACGACGGAAGGACGGAC
GGTCGCCGCCACGGTCGTCACGAC	GGGGGTACGAGGGGCGGTCGCCGCCACGGTCGTCACGGCGCGGGTAGGAGGGGC
GGTCGCCACCACGGTCATCGCGGC	GCGGGTACGAGGGACGGTCGCCACCACGGTCGTCACGGCGCGGGTAGGACGGGC
GGTCGCCACCACGGTCATCACGAC	GGAAGGACGGGCGGTCGCCACCGCCGGCGGGACGCCCACCACGGTCGTCGCGACGGTAGCCACCGCCGCTGCCTGCCG
GGCGGCCACCGCGGTCGTCACGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_173675216.1|2090087_2090918_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224045
NZ_CP019798.1|WP_078093953.1|2091957_2093016_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl|CDD|182464
NZ_CP019798.1|WP_078093957.1|2110030_2110813_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030855349.1|2094253_2095525_+|DUF1015-domain-containing-protein	unknown	unknown	gnl|CDD|377633
NZ_CP019798.1|WP_060179947.1|2087520_2088429_-|NAD-kinase	unknown	unknown	gnl|CDD|235121
NZ_CP019798.1|WP_030849811.1|2105418_2105955_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	unknown	unknown	gnl|CDD|182339
NZ_CP019798.1|WP_030849804.1|2107507_2108494_-|SPFH/Band-7/PHB-domain-protein	unknown	unknown	gnl|CDD|223407
NZ_CP019798.1|WP_078093956.1|2103719_2104361_-|DNA-3-methyladenine-glycosylase	unknown	unknown	gnl|CDD|376746
NZ_CP019798.1|WP_060181149.1|2106645_2107416_-|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl|CDD|376667
NZ_CP019798.1|WP_076044059.1|2093065_2094166_-|HAD-IIA-family-hydrolase	unknown	unknown	gnl|CDD|319832
NZ_CP019798.1|WP_078093954.1|2095595_2096447_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|367841
NZ_CP019798.1|WP_076044062.1|2089631_2089979_+|SCP2-sterol-binding-domain-containing-protein	unknown	unknown	gnl|CDD|379708
NZ_CP019798.1|WP_030849799.1|2109102_2109897_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224044
NZ_CP019798.1|WP_030849801.1|2108578_2109007_-|NfeD-family-protein	unknown	unknown	gnl|CDD|224501
NZ_CP019798.1|WP_060180004.1|2089248_2089509_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030849815.1|2104469_2105252_+|sporulation-protein	unknown	unknown	gnl|CDD|369195
NZ_CP019798.1|WP_030855338.1|2088425_2089241_-|TlyA-family-RNA-methyltransferase	unknown	unknown	gnl|CDD|224110
NZ_CP019798.1|WP_051700791.1|2090914_2091916_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl|CDD|227119
NZ_CP019798.1|WP_030849808.1|2106104_2106608_+|HNH-endonuclease	unknown	unknown	gnl|CDD|224321
NZ_CP019798.1|WP_159425524.1|2110980_2111262_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_173675216.1|2090087_2090918_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224045	COG1120, FepC, ABC-type cobalamin/Fe3+-siderophores transport systems, ATPase components [Inorganic ion transport and metabolism / Coenzyme metabolism].	5.18091e-137
NZ_CP019798.1|WP_078093953.1|2091957_2093016_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl|CDD|182464	PRK10441, PRK10441, Fe(3+)-siderophore ABC transporter permease.	1.22075e-98
NZ_CP019798.1|WP_030855349.1|2094253_2095525_+|DUF1015-domain-containing-protein	gnl|CDD|377633	pfam06245, DUF1015, Protein of unknown function (DUF1015). Family of proteins with unknown function found in archaea and bacteria.	2.47779e-121
NZ_CP019798.1|WP_060179947.1|2087520_2088429_-|NAD-kinase	gnl|CDD|235121	PRK03372, ppnK, inorganic polyphosphate/ATP-NAD kinase; Provisional.	3.39084e-171
NZ_CP019798.1|WP_030849811.1|2105418_2105955_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	gnl|CDD|182339	PRK10257, PRK10257, putative kinase inhibitor protein; Provisional.	2.44995e-62
NZ_CP019798.1|WP_030849804.1|2107507_2108494_-|SPFH/Band-7/PHB-domain-protein	gnl|CDD|223407	COG0330, HflC, Membrane protease subunits, stomatin/prohibitin homologs [Posttranslational modification, protein turnover, chaperones].	3.29738e-69
NZ_CP019798.1|WP_078093956.1|2103719_2104361_-|DNA-3-methyladenine-glycosylase	gnl|CDD|376746	pfam02245, Pur_DNA_glyco, Methylpurine-DNA glycosylase (MPG). Methylpurine-DNA glycosylase is a base excision-repair protein. It is responsible for the hydrolysis of the deoxyribose N-glycosidic bond, excising 3-methyladenine and 3-methylguanine from damaged DNA.	2.96864e-84
NZ_CP019798.1|WP_060181149.1|2106645_2107416_-|sulfite-exporter-TauE/SafE-family-protein	gnl|CDD|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	2.97621e-23
NZ_CP019798.1|WP_076044059.1|2093065_2094166_-|HAD-IIA-family-hydrolase	gnl|CDD|319832	cd07530, HAD_Pase_UmpH-like, UmpH/NagD family phosphatase, similar to Escherichia coli UmpH UMP phosphatase/NagD nucleotide phosphatase and Mycobacterium tuberculosis Rv1692 glycerol 3-phosphate phosphatase. Escherichia coli UmpH/NagD is a ribonucleoside tri-, di-, and monophosphatase with a preference for purines, it shows peak activity with UMP and functions in UMP-degradation. It is also an effective phosphatase with AMP, GMP and CMP. Mycobacterium tuberculosis phosphatase, Rv1692 is a glycerol 3-phosphate phosphatase. Rv1692 is the final enzyme involved in glycerophospholipid recycling/catabolism. This subfamily belongs to the UmpH/NagD phosphatase family, and to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	7.26143e-98
NZ_CP019798.1|WP_078093954.1|2095595_2096447_-|tetratricopeptide-repeat-protein	gnl|CDD|367841	pfam04147, Nop14, Nop14-like family. Emg1 and Nop14 are novel proteins whose interaction is required for the maturation of the 18S rRNA and for 40S ribosome production.	2.39923e-06
NZ_CP019798.1|WP_076044062.1|2089631_2089979_+|SCP2-sterol-binding-domain-containing-protein	gnl|CDD|379708	pfam14864, Alkyl_sulf_C, Alkyl sulfatase C-terminal. This domain is found at the C-terminus of alkyl sulfatases. Together with the N-terminal catalytic domain, this domain forms a hydrophobic chute and may recruit hydrophobic substrates.	7.13199e-06
NZ_CP019798.1|WP_030849799.1|2109102_2109897_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224044	COG1119, ModF, ABC-type molybdenum transport system, ATPase component/photorepair protein PhrA [Inorganic ion transport and metabolism].	1.5997e-92
NZ_CP019798.1|WP_030849801.1|2108578_2109007_-|NfeD-family-protein	gnl|CDD|224501	COG1585, COG1585, Membrane protein implicated in regulation of membrane protease activity [Posttranslational modification, protein turnover, chaperones / Intracellular trafficking and secretion].	1.48338e-17
NZ_CP019798.1|WP_030849815.1|2104469_2105252_+|sporulation-protein	gnl|CDD|369195	pfam07070, Spo0M, SpoOM protein. This family consists of several bacterial SpoOM proteins which are thought to control sporulation in Bacillus subtilis.Spo0M exerts certain negative effects on sporulation and its gene expression is controlled by sigmaH.	9.0595e-108
NZ_CP019798.1|WP_030855338.1|2088425_2089241_-|TlyA-family-RNA-methyltransferase	gnl|CDD|224110	COG1189, COG1189, Predicted rRNA methylase [Translation, ribosomal structure and biogenesis].	5.85228e-101
NZ_CP019798.1|WP_051700791.1|2090914_2091916_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl|CDD|227119	COG4779, FepG, ABC-type enterobactin transport system, permease component [Inorganic ion transport and metabolism].	1.74868e-101
NZ_CP019798.1|WP_030849808.1|2106104_2106608_+|HNH-endonuclease	gnl|CDD|224321	COG1403, McrA, Restriction endonuclease [Defense mechanisms].	1.04476e-15

Protein sequences

>NZ_CP019798.1|WP_078093954.1|2095595_2096447_-|tetratricopeptide-repeat-protein
MRQELLSLPKGLAEEVSKNLVMVARLIDEDPEQAYAYSRIALRLASRVAAVREAAGFAAYATQKYSEALAEFRAAKRMTGSVELWPVMADCERGLGRPERALAMAGEPEVQKLDKAGQVEMRLVAAGARRDQGQLEAAIVTLQSPELASNAVQPWTARLRYAYADALLAAGREDEAREWFGKALEADKDGATDASDRLAELDGVEFVDAAIDLSDDDEVEDLTAGDRDEDDDEDDDEDEDPAEVAAAERATDVTEYYDEDDEEFEPLEQSAAGADTDLRGDQA
>NZ_CP019798.1|WP_030855349.1|2094253_2095525_+|DUF1015-domain-containing-protein
MTTSGTADHGLRLIPFHGLRYVPERVGSLAAVTSPPYDVVVRPDGVDHLESADPHNIVRLILPQAGTPAARNEQAARTLRDWLAEGILSADPEPALYVYEQRRAGLLQRGVIGALALSTADAGIVLPHEDVMPDVVTDRAGLMRATSANLEPLLLTYRGDDPAAGAAAVVERTAQHPPLLSTTTEDGFQHRLWAITDPAELAAVTADLSHRQALIADGHHRWATYLRLQEEHGSPTAWDFGLVLLVDTARYPLQVRAIHRMLRRLPVADALAAVAGHFRVRPVDGPLPLALDALADAAERGNAFLLAGDGAFHLVTDPDLALLDRTVRHDRPEAWRRLDATVLHATLLDALWHVPDAPDQITYIHDAASTVAMAERHGGTAVLLHPVREEVVRDLARQGVTMPRKSTSFGPKPATGLVLRGLG
>NZ_CP019798.1|WP_076044059.1|2093065_2094166_-|HAD-IIA-family-hydrolase
MTRQIRTSPAACDESLHQAYDTALLDLDGVVYAGGRAIGHAVESLAAARAAGMHLAYVTNNALRTPEAVAEHLGELGIPTDAAEVITSAQAVARLIAEQVEPGSKVLVIGGEGLRVALRERGLVPVESADEEGLAAVVQGYGGPDLAWGRFAEASYAINRGVPWYASNTDLTIPGARGIAPGNGAAVEVVRIATGAEPQVAGKPLPPMHRETVLRTGAKRPLVVGDRLDTDIEGAFNGEVDSLLVLTGVTDAEQLLRAEPRHRPTYVDRDLRGLLAGQPEVVPAAEGFRCGGWTAVALNNGLLDLREADEDSGEGPTTGDGATTGDGGPGPDPLDGLRALCAAAWTAAADGVCTLDAAKALARLGL
>NZ_CP019798.1|WP_078093953.1|2091957_2093016_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MLVESPPESGPSAPPPPDAVARPRHAARAAGLAGALVVLALIAVLSIAVGAKQMPLDEVWHGLFHYSGTTSDVVVRDLRVPRTLLGLMVGLGLGLSGAVMQALTRNPLAEPGILGVNAGAAAAVVSAISFFGASSLGEFVWWAFLGAAVVSVLVYVLGGSRSATPVRLALAGTAASAALVGYINAVQLMDSKALDKLRFWTVGSLASANMDTVRQVAPFLLVGAVLALSLGRPLNAMAMGDDTARALGANLTRTRVGAMLAITLLCGAATAACGPIVFIGLMIPHLVRVFTGPDMRWVLAYSAVLSPVLLLGADVAGRVVTRPAELQVGIVTALIGGPVFIYLVRRKRMAQL
>NZ_CP019798.1|WP_051700791.1|2090914_2091916_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MSLRIERRALAVGALLVLAAFVMAVLLIGTGDFDIAPWDVVQTLLGNGTPAHDFIVNDLRLPRVLVALLVGAALGMAGAVFQSVTRNPLGSPDLLGFSYGSAVGALVVIILLKGSATEVAAGALLGGLLAGAAVYLLAYKRGIHGYRLVLVGIGASAMLLAVIQYLITKAQLVEASRAMVWLTGSLAGRDWAQVWPLLATCAVLFPLVLGQSRALRMIEMGDDAAYAVGVRVERTRLLLMLAAILLTTAASAAAGPISFVALAAPQLARRLTGSPGANLLSAALMGSVVLLLSDWASQRAFGADQLPVGVVTGLVGGVYLLWLLVTERKAGRI
>NZ_CP019798.1|WP_173675216.1|2090087_2090918_-|ABC-transporter-ATP-binding-protein
MNLRSAQVQRLTAENVTLGYDQRVIAENLSVEIPDNSFTVIVGPNACGKSTLLRALSRMLKPSQGRVLLDGQAIGSLPAKKVAKTLGLLPQSSIAPDGITVADLVSRGRYPHQGLLRQWSHEDERIVTESMASTGVAELADRAVDELSGGQRQRVWIAMALAQQTPLLLLDEPTTYLDIQHQIDVLDLCAELHETQGRTLVAVLHDLNHAARYATHLIAMRGGKVIAEGPPQEVVTAELVEKVFGLRCQVIDDPETGTPLVIPAARRSRAQAAAEV
>NZ_CP019798.1|WP_076044062.1|2089631_2089979_+|SCP2-sterol-binding-domain-containing-protein
MATIQECREALDRLSDNLARAEEGVRGAAAFDRSLSCHITDLAQTFTGRLEGGRIRVDAVAPGPPARKAEIRLAMTGDDLVALVAGELKFAKAWASGRVRLEAGFRDLLRLKSLL
>NZ_CP019798.1|WP_060180004.1|2089248_2089509_-|hypothetical-protein
MRAEAGAAAAEAPAEPVEPAGPAALGVVRTPTGHAGVDAHLARLADADHLAADGHVEVYEDVHRGLREALTALDAPPVPGPYENRS
>NZ_CP019798.1|WP_030855338.1|2088425_2089241_-|TlyA-family-RNA-methyltransferase
MAGVARRRLDAELVRRSMARSREHAAQLIAAGRVTVGGTTATKAATQVETSAALVVLKDDADPDYVSRGGHKLAGALAAFLPRGLRVEGRRALDAGASTGGFTDVLLRAGVAHVMAVDVGYGQLAWSLQSDDRVTVKDRTNVRELTVEQIDGIPVDLVVGDLSFISIGLVLPALVRCTAPDADLVLMVKPQFEVGKDRLGSGGVVRSPELRAEAVREVAASAAALGLGVLGVTASPLPGPSGNVEYFLWLRAGAPALDPADVDRAVAEGPQ
>NZ_CP019798.1|WP_060179947.1|2087520_2088429_-|NAD-kinase
MTDSSGERTVFLLAHTGRPAAIRSAELVVKGLLRCGLGVRVFDHEAVDLPLPPEVELVTESTPGVLDGCELLVVLGGDGTLLRGAELARASGVPMLGVNLGRVGFLAEAERDDLDKVVDRVVTRSYEVEERMTLDVIVRTNGDVVHRDWALNEAAVQKVSPERMLEVVLEIDGRPVTGFGCDGIVCATPTGSTAYAFSAGGPVVWPEVEALLMVPISAHALFAKPLVTSPNSVLAVEVQSGTPHGVLWCDGRRMLELPAGARVEVRRGAVPVRLARLHHASFTDRLVAKFALPVSGWRGAPH
>NZ_CP019798.1|WP_078093956.1|2103719_2104361_-|DNA-3-methyladenine-glycosylase
MSARLDRTPLARSFFDRPVLTVAPDLLGRTLVRRTEEGLMELRITEVEAYEGEADPGSHAYRGRTARNASMFGPPGHAYVYFIYGMWFSLNLVCGPPGHASGVLLRAGEITVGADLAAKRRVSARNPRELAKGPARLATALDVDRSLDGTDLCAGPGSPLSLLAGTPTSADLVSSGPRTGVGGAGADHPYRFWITHDPTVSPYRAHAPRRRST
>NZ_CP019798.1|WP_030849815.1|2104469_2105252_+|sporulation-protein
MGFKKLFASLGAGGASVDTIITEPNVVPGGIVQGEVRIQGGSVEQQIEGLSVGLQARVEVEGGDQEYKQDVVFTKQRLGGAFQVQAGALHVVPFALEIPWETPITHYAGQHLHGMNIGVSTELEIARAVDAGDLDAINVHPVPAQQAILDAFRQLGFTFRSADMERGHIRGTRQTLPFYQEIEFLPPSQYRGLHQVELTFVSDGREMDVVLEMDKKPGLFSEGSDTYRCFQVGLQSYQGTDWAAYLNQWIASVGSQRNWF
>NZ_CP019798.1|WP_030849811.1|2105418_2105955_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein
MSERDRAPLPHDFHPEVHEFTVTSEDVSHGADLNAAQVLTGKNISPHLRWEGFPEGTKSFAVTCFDPDAPTGSGFWHWVLFDLPVSVTELPAGAGTGDFPGLPEGAVHARNDYGTRDFGGAAPPRGERHRYVFTVYAVDREQLGPDEDSSPAVVGFHLRFHALGRAQLVAEYEAPAAR
>NZ_CP019798.1|WP_030849808.1|2106104_2106608_+|HNH-endonuclease
MRDTLVLNASFEPLSTVTLNRAVVLVLQDKAVVEQSHPDLRVRAATMDLPMPRVIRLCRYVRVPFRRHAPWSRRGVLVRDQHRCAYCGKRATTVDHVLPRAQGGGDTWLNTVASCADDNHRKAARTPEEAGMPLLRKPFVPSPADAMLLALGVAGQEGLPEWLERSA
>NZ_CP019798.1|WP_060181149.1|2106645_2107416_-|sulfite-exporter-TauE/SafE-family-protein
MSIWESLAVLTAGIGAGTINTIVGSGTLITFPVLLATGLPPVTANVSNTLGLVPGSISGAIGYRKELRGQRARILRLGSVSAVGGLAGAALLLALPSESFDTIVPVLIGLALVLVVLQPRLAAALRRRQEAAGGDTGHPDGGPLLLGGMLFSSAYGGYFGAAQGVLYLGLMGLLLHDDLQRVNAVKNVIAALVNGIAAVFFLFVAEFDWTAVLLIAVGSTIGGQIGAKVGRRLSPTVLRAVIVTVGLLAIVQLLTH
>NZ_CP019798.1|WP_030849804.1|2107507_2108494_-|SPFH/Band-7/PHB-domain-protein
MQPIIIVLIILVVLVFIALVKTIQVIPQASAAIVERFGRYTRTLNAGLNIVVPFIDSIRNRIDLREQVVPFPPQPVITQDNLVVNIDTVIYYQVTDARAATYEVASYIQAIEQLTVTTLRNIIGGMDLERTLTSREEINAALRGVLDEATGKWGIRVNRVELKAIEPPTSIQDSMEKQMRADRDKRAAILQAEGVRQSEILRAEGEKQSSILRAEGEAKAAALKAEGEAQAIRTVFESIHAGDADQKLLAYQYLQMLPKIAEGDANKLWIVPSEIGDALKGLSGAMGNFGPLGGGSGFNPQNSGKDGGGIPAARDKDSAERREQPPID
>NZ_CP019798.1|WP_030849801.1|2108578_2109007_-|NfeD-family-protein
MDIDAWVWWLIGAVGLGIPLVLTAMPEFGMFAVGAVAAAVTAALGGGVVAQVLVFVVVSVALIAVVRPIANRHRDQRPQHRSGIDALRGRTAVVLERVDGGGGRIKLAGEVWSARALDADTIFEPGQSVDVVEIDGATAVVM
>NZ_CP019798.1|WP_030849799.1|2109102_2109897_-|ABC-transporter-ATP-binding-protein
MSDVLELVDVSVVREGRALVDQVSWSVKEGERWVILGPNGAGKTTLLNLASSYLFPTKGSATILGSTLGKVDVFELRPRIGMAGIAMADKLPKRQTVLQTVLTAAYGMTATWQEEYEAVDEQRARAFLDRLGMTEYLDRKFGTLSEGERKRTLIARALMTDPELLLLDEPAAGLDLGGREDLVRRLGRLARDPLAPSMVMVTHHVEEIAPGFTHVLMIRQGKVVTAGPIDLELTSRNLSLCFGLPLVVERNGADRWTAQGLPLG
>NZ_CP019798.1|WP_078093957.1|2110030_2110813_+|hypothetical-protein
MLFEPRSGRLAAWGNALLAGLASPDEAAMSIVGEDAVHRVEGLPGESGPVGLTLGLGRLRALGVSGLRVALPAPGHPLGLSAPPEFNARALEAEEAVVAVGAALGLVPEVAEAGPAGDVHVSVTWHCLPVREAPPADVPSLGEAERELAEALREATAVLTRLDVAGSGPVAEAALSAYRARAEAGQDALAPGYPPRAVRVLALAQRVDLMVSLAYESGHGGAVAASEMAARAEALRPVERVARRALVAAYNSAVEARERD
>NZ_CP019798.1|WP_159425524.1|2110980_2111262_-|hypothetical-protein
MVDTRTRTVVKTVGVGHEPSRMRSPRTTGASRLRTPGPGGDTRRPHAVRRHRRRRPRLGSAPPPARPPTASPSAADPPPWPSPRTADTSTSPT

Crispr_ID: NZ_CP019798_5

• CRISPR_ID: NZ_CP019798_5
• CRISPR_location: 2478714-2478857
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_5

Consensus_repeat	Method
CCGGCACCGGCACGGCCCGACCCCGCCAGGGGTACCGGCCACCGCC	CRISPRCasFinder

spacers of NZ_CP019798_5

>5.1|2478760|52|NZ_CP019798|CRISPRCasFinder
GACCACCGCCCGGGGGCCCGGCCCCCACACCGCCCAGCCCCCGGCACCGGCA

CRISPR arrays and Neighbor proteins around NZ_CP019798_5

CRISPR arrays

The CRISPR arrays of NZ_CP019798_5

>merge|NZ_CP019798|5|2478714-2478857|CRISPRCasFinder
CCGGCACCGGCACGGCCCGACCCCGCCAGGGGTACCGGCCACCGCCGACCACCGCCCGGGGGCCCGGCCCCCACACCGCCCAGCCCCCGGCACCGGCACCGGCACCGGCACGGCACGACCCCGCCAGGGGTACCGGCCACCGCC

>NZ_CP019798|5|2|2478714-2478857|CRISPRCasFinder
CCGGCACCGGCACGGCCCGACCCCGCCAGGGGTACCGGCCACCGCC	GACCACCGCCCGGGGGCCCGGCCCCCACACCGCCCAGCCCCCGGCACCGGCA
CCGGCACCGGCACGGCACGACCCCGCCAGGGGTACCGGCCACCGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_030850089.1|2476648_2477383_+|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|366759
NZ_CP019798.1|WP_060178189.1|2481941_2483570_-|ubiquinol-cytochrome-c-reductase-cytochrome-b-subunit	unknown	unknown	gnl|CDD|379304
NZ_CP019798.1|WP_030849368.1|2483566_2484625_-|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl|CDD|239550
NZ_CP019798.1|WP_030850095.1|2473595_2474624_-|C40-family-peptidase	unknown	unknown	gnl|CDD|366353
NZ_CP019798.1|WP_030850092.1|2474876_2476241_-|NYN-domain-containing-protein	unknown	unknown	gnl|CDD|377585
NZ_CP019798.1|WP_078094073.1|2468205_2469819_-|GMC-family-oxidoreductase	unknown	unknown	gnl|CDD|225186
NZ_CP019798.1|WP_008738811.1|2476284_2476524_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030849356.1|2488152_2488551_-|cytochrome-c-oxidase-subunit-4	unknown	unknown	gnl|CDD|378833
NZ_CP019798.1|WP_078094076.1|2478871_2480287_-|aminotransferase-class-V-fold-PLP-dependent-enzyme	unknown	unknown	gnl|CDD|223594
NZ_CP019798.1|WP_030849374.1|2480713_2481778_-|anthranilate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234682
NZ_CP019798.1|WP_078094078.1|2486776_2488021_-|L,D-transpeptidase-family-protein	unknown	unknown	gnl|CDD|380079
NZ_CP019798.1|WP_078094077.1|2486327_2486732_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030036316.1|2484621_2485431_-|c-type-cytochrome	unknown	unknown	gnl|CDD|129864
NZ_CP019798.1|WP_076044994.1|2472309_2473374_-|C40-family-peptidase	unknown	unknown	gnl|CDD|366353
NZ_CP019798.1|WP_078094075.1|2471112_2472243_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_060178191.1|2488547_2490278_-|cytochrome-c-oxidase-subunit-I	unknown	unknown	gnl|CDD|238832
NZ_CP019798.1|WP_030850108.1|2466363_2468160_+|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|341233
NZ_CP019798.1|WP_030850086.1|2477379_2477661_+|Lrp/AsnC-ligand-binding-domain-containing-protein	unknown	unknown	gnl|CDD|366431
NZ_CP019798.1|WP_078094074.1|2469949_2471092_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_CP019798.1|WP_030849365.1|2485507_2486128_-|heme-copper-oxidase-subunit-III	unknown	unknown	gnl|CDD|224758

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_030850089.1|2476648_2477383_+|rhomboid-family-intramembrane-serine-protease	gnl|CDD|366759	pfam01694, Rhomboid, Rhomboid family. This family contains integral membrane proteins that are related to Drosophila rhomboid protein. Members of this family are found in bacteria and eukaryotes. Rhomboid promotes the cleavage of the membrane-anchored TGF-alpha-like growth factor Spitz, allowing it to activate the Drosophila EGF receptor. Analysis has shown that Rhomboid-1 is an intramembrane serine protease (EC:3.4.21.105). Parasite-encoded rhomboid enzymes are also important for invasion of host cells by Toxoplasma and the malaria parasite.	6.75517e-26
NZ_CP019798.1|WP_078094073.1|2468205_2469819_-|GMC-family-oxidoreductase	gnl|CDD|225186	COG2303, BetA, Choline dehydrogenase and related flavoproteins [Amino acid transport and metabolism].	9.44488e-22
NZ_CP019798.1|WP_030849368.1|2483566_2484625_-|Rieske-2Fe-2S-domain-containing-protein	gnl|CDD|239550	cd03467, Rieske, Rieske domain; a [2Fe-2S] cluster binding domain commonly found in Rieske non-heme iron oxygenase (RO) systems such as naphthalene and biphenyl dioxygenases, as well as in plant/cyanobacterial chloroplast b6f and mitochondrial cytochrome bc(1) complexes. The Rieske domain can be divided into two subdomains, with an incomplete six-stranded, antiparallel beta-barrel at one end, and an iron-sulfur cluster binding subdomain at the other. The Rieske iron-sulfur center contains a [2Fe-2S] cluster, which is involved in electron transfer, and is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In RO systems, the N-terminal Rieske domain of the alpha subunit acts as an electron shuttle that accepts electrons from a reductase or ferredoxin component and transfers them to the mononuclear iron in the alpha subunit C-terminal domain to be used for catalysis.	2.46355e-21
NZ_CP019798.1|WP_030850095.1|2473595_2474624_-|C40-family-peptidase	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	8.72566e-30
NZ_CP019798.1|WP_030850086.1|2477379_2477661_+|Lrp/AsnC-ligand-binding-domain-containing-protein	gnl|CDD|366431	pfam01037, AsnC_trans_reg, Lrp/AsnC ligand binding domain. The l-leucine-responsive regulatory protein (Lrp/AsnC) family is a family of similar bacterial transcription regulatory proteins. The family is named after two E. coli proteins involved in regulating amino acid metabolism. This entry corresponds to the usually C-terminal regulatory ligand binding domain. Structurally this domain has a dimeric alpha/beta barrel fold.	1.2322e-13
NZ_CP019798.1|WP_060178189.1|2481941_2483570_-|ubiquinol-cytochrome-c-reductase-cytochrome-b-subunit	gnl|CDD|379304	pfam13631, Cytochrom_B_N_2, Cytochrome b(N-terminal)/b6/petB.	4.10458e-67
NZ_CP019798.1|WP_030849356.1|2488152_2488551_-|cytochrome-c-oxidase-subunit-4	gnl|CDD|378833	pfam12270, Cyt_c_ox_IV, Cytochrome c oxidase subunit IV. This family of proteins is found in bacteria. Proteins in this family are approximately 140 amino acids in length. This family is the fourth subunit of the cytochrome c oxidase complex. This subunit does not have a catalytic capacity but instead, is required for assembly and/or stability of the complex.	6.5184e-63
NZ_CP019798.1|WP_078094076.1|2478871_2480287_-|aminotransferase-class-V-fold-PLP-dependent-enzyme	gnl|CDD|223594	COG0520, csdA, Selenocysteine lyase/Cysteine desulfurase [Posttranslational modification, protein turnover, chaperones].	6.56495e-94
NZ_CP019798.1|WP_030849374.1|2480713_2481778_-|anthranilate-phosphoribosyltransferase	gnl|CDD|234682	PRK00188, trpD, anthranilate phosphoribosyltransferase; Provisional.	6.08614e-167
NZ_CP019798.1|WP_078094078.1|2486776_2488021_-|L,D-transpeptidase-family-protein	gnl|CDD|380079	pfam17964, Big_10, Bacterial Ig domain. This entry represents a bacterial Ig-like domain found associated with transpeptidase domains.	3.64383e-44
NZ_CP019798.1|WP_030036316.1|2484621_2485431_-|c-type-cytochrome	gnl|CDD|129864	TIGR00782, di-heme_cytochrome_cp, cytochrome c oxidase, cbb3-type, subunit III. This model describes a di-heme subunit of approximately 26 kDa of the cbb3 type copper and heme-containing cytochrome oxidase. [Energy metabolism, Electron transport].	3.00616e-14
NZ_CP019798.1|WP_076044994.1|2472309_2473374_-|C40-family-peptidase	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	4.42181e-33
NZ_CP019798.1|WP_060178191.1|2488547_2490278_-|cytochrome-c-oxidase-subunit-I	gnl|CDD|238832	cd01662, Ubiquinol_Oxidase_I, Ubiquinol oxidase subunit I. Ubiquinol oxidase, the terminal oxidase in the respiratory chains of aerobic bacteria, is a multi-chain transmembrane protein located in the cell membrane. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. The number of subunits in ubiquinol oxidase varies from two to five. Subunit I contains a heme-copper binuclear center (the active site where O2 is reduced to water) formed by a high-spin heme and a copper ion. It also contains a low-spin heme, believed to participate in the transfer of electrons from ubiquinol to the binuclear center. For every reduction of an O2 molecule, eight protons are taken from the inside aqueous compartment and four electrons are taken from ubiquinol on the opposite side of the membrane. The four electrons and four of the protons are used in the reduction of O2; the four remaining protons are pumped across the membrane. This charge separation of four charges contributes to the electrochemical gradient used for ATP synthesis. Two proton channels, the D-pathway and K-pathway, leading to the binuclear center have been identified in subunit I. It is generally believed that the channels contain water molecules that act as 'proton wires' to transfer the protons. A well-defined pathway for the transfer of pumped protons beyond the binuclear center has not been identified. Electrons are believed to be transferred directly from ubiquinol (the electron donor) to the low-spin heme, and directly from the low-spin heme to the binuclear center.	0
NZ_CP019798.1|WP_030850108.1|2466363_2468160_+|long-chain-fatty-acid--CoA-ligase	gnl|CDD|341233	cd05907, VL_LC_FACS_like, Long-chain fatty acid CoA synthetases and Bubblegum-like very long-chain fatty acid CoA synthetases. This family includes long-chain fatty acid (C12-C20) CoA synthetases and Bubblegum-like very long-chain (>C20) fatty acid CoA synthetases. FACS catalyzes the formation of fatty acyl-CoA in a two-step reaction: the formation of a fatty acyl-AMP molecule as an intermediate, and the formation of a fatty acyl-CoA. Eukaryotes generally have multiple isoforms of LC-FACS genes with multiple splice variants. For example, nine genes are found in Arabidopsis and six genes are expressed in mammalian cells. Drosophila melanogaster mutant bubblegum (BGM) have elevated levels of very-long-chain fatty acids (VLCFA) caused by a defective gene later named bubblegum. The human homolog (hsBG) of bubblegum has been characterized as a very long chain fatty acid CoA synthetase that functions specifically in the brain; hsBG may play a central role in brain VLCFA metabolism and myelinogenesis. Free fatty acids must be "activated" to their CoA thioesters before participating in most catabolic and anabolic reactions.	0
NZ_CP019798.1|WP_030850092.1|2474876_2476241_-|NYN-domain-containing-protein	gnl|CDD|377585	pfam05991, NYN_YacP, YacP-like NYN domain. This family consists of bacterial proteins related to YacP. This family is uncharacterized functionally, but it has been suggested that these proteins are nucleases due to them containing a NYN domain. NYN (for N4BP1, YacP-like Nuclease) domains were discovered by Anantharaman and Aravind. Based on gene neighborhoods it was suggested that the bacterial YacP proteins interact with the Ribonuclease III and TrmH methylase in a processome complex that catalyzes the maturation of rRNA and tRNA.	9.41884e-13
NZ_CP019798.1|WP_078094074.1|2469949_2471092_-|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.	3.85212e-69
NZ_CP019798.1|WP_030849365.1|2485507_2486128_-|heme-copper-oxidase-subunit-III	gnl|CDD|224758	COG1845, CyoC, Heme/copper-type cytochrome/quinol oxidase, subunit 3 [Energy production and conversion].	1.41056e-54

Protein sequences

>NZ_CP019798.1|WP_030850086.1|2477379_2477661_+|Lrp/AsnC-ligand-binding-domain-containing-protein
MITAIVLIKTSVDRIPEIAESIAALDNVSEVYSVTGTYDLIALVRVNRHENLADIIPGRISKIPGVEATDTHVAFRTYSQHDLEAAFAIGLDA
>NZ_CP019798.1|WP_030850089.1|2476648_2477383_+|rhomboid-family-intramembrane-serine-protease
MLCHMIVRWRALREAARGPVVTHALIAGCGVVFALSPASGLNPAYGTGDELLAAGTAYFRRWGVVPDELFTDTPRAWLTPLTALFVHGSWLHLLGNMLFLFVFGALAEERMGRPAFLVFYLCTGYLALAAYAAANADSAQTLVGASGAISAVLGAFLFLLPRARVTSLFPFLFFLPLRFPAWMVLLFWFALQWVAAHRAESGPGVAYLAHLVGFSLGFLYAWARYRGTTRVRRPATATEGDSQP
>NZ_CP019798.1|WP_008738811.1|2476284_2476524_-|hypothetical-protein
MTVPLPTDTTRWRCTLCGNLTRFDVTRSSKVVEYVHLDLAGEPKVEEREVVNETIESVRCRWCNAVDQIELVDRPGADS
>NZ_CP019798.1|WP_030850092.1|2474876_2476241_-|NYN-domain-containing-protein
MVEPASGAGPADAAGDAAEALDRPLPEGVRRRVVALVSDAFGALTVADLPAQLRQYARFTPTRRAKFAGNAMAAAVETDPVFRSRVAEKVREAQADLAGALESGAPPAAADPLDVAAAAFVLRPAGWVKLVAAAGEEAQRADAERVGEETRRELERLREELEHVRELQRTGGEQVRVELEAARKEAESLQRRLRSALSDVKRGEAALRKVTAEIDGIRGEAATRVAAAESESRRLKSRLAEVETALETSRRATREGRSIEDMRLRLLLDTVLDAAQGLRRELALPPVNTRPADTVDAVEPGRMTPKDIAARALSETDPALLDQLLALPQAHLVVDGYNVTKTGYPTMPLEKQRLRLLGGLSMLAAQTGAEMTCVFDGAELAAPVLLAPPRGVRVLFSKAGVTADELIRQLVRAEPPGRPVVVVSTDREVADGVAKAGARPVTSALLLKRLSRVS
>NZ_CP019798.1|WP_030850095.1|2473595_2474624_-|C40-family-peptidase
MASHRRPKQPTRARVTVLTSVAAAAVALTAQSASAAPAKPSKDEVKSQVDALYEEAEQATEKFNGAKERQATLEKEIGQIQDQVARGQSELNDLRSALGSMASAQYRSGGIDPSLALLLSADPDGYLDKASTLEHLSGKQVEAVQKIQAKQRTLAQQRQEASGKLADLDATRKELAEKKKVSSEKLAAAQAILNTLTAQERAALKDEETRASRAAGQRVDLGDVKASGRAGAALAAAKTKVGSAYISGHEGPNSFDCSGLTQWAYKQAGVNISRVTYTQANDGTRISRSQLQPGDLVFFYGDLHHVGLYAGNNMTLHASNPRGGVKYESMDNMPFQFGVRIG
>NZ_CP019798.1|WP_076044994.1|2472309_2473374_-|C40-family-peptidase
MASHRRTGLGGLDRNTKVTVLTAAAATAAVAMAAAPAGAAPGHPHEPGGSARSGVSAQVDRLFEEAEQATEHFNEAGEKADRLRVEVNRAQDAVARGQERINTMRGVLGTFAGAQYRSGGIDPAVGLMLAEDPDAYLEQAAALDRLTERQARQLHELRQEQRRLGQVRSEASRKLAELDALRSDVARHKRSVTAKLAAAQRLLNSMPSEERADFERSSRSGGRHEALPDLGPMGAGGPSSGRAAAAVMAARAAVGRPYVWGSTGPSGFDCSGLMVWSYRQAGVSLPRTSQAQRHAGRQVPLSQARPGDLVTYRSDASHVGMYVGNGQVVHAPYPGARVRYDPVGMMPVSAVTRP
>NZ_CP019798.1|WP_078094075.1|2471112_2472243_-|hypothetical-protein
MLPVRRPPRILPLVALLLGVLLAGCGPQPAGSADTAEREVRRAVADWSRTVPEALAGIPLTDWAYEVSSVRRDGARALAAARLRYRLAGYDTAPEESAREVELVREDGAWRVGADRPAPGALPQLWDQGPVSVAAGTHSLVLGGAGQSAGTLREIAAEADRAVPAASAAWPGPWAGRVVVLVPGSLDAMARLLGRPADTYRGLGAVTTGRVGAGPAPADRVVVNPEGYAGLGAEGRRIILTHEVAHVATRAATSATTPLWLSEGFADWAAYRGAAAAPAQAAPALARAVRRGELPGELPRTEDFAFGGDPDAAARAYEGAWLACRLIAAEWGGKALVELYGRAGRESLETALRSTLGVDRAGLTQAWQESLRGELR
>NZ_CP019798.1|WP_078094074.1|2469949_2471092_-|glycosyltransferase-family-4-protein
MHKTLIVTNDFPPRPGGIQAFLHNMALRLDPDRVVVYASTWKHGAEGREATAAFDAEQPFQVVRDRTTMLLPTPRVTRRAVGLLREHGCESVWFGAAAPLGLMGPALRRAGARRIVATTHGHEAGWAQLPAARQLLRRIGEGTDTLTYLGEYTRSRIASAVTGRAAARMVQLPPGVDEKTFHPASGGDEVRARLGLADRPVVVCVSRLVPRKGQDTLIESMPRILAAVPDAVLLIVGGGPYEADLRALAQSTGVARSVVFTGAVPWSELPAHYGAGDVFAMPCRTRRGGLDVEGLGIVYLEASATGLPVVAGDSGGAPDAVLDGETGWVVRGGAPEEAADRITALLQDPDLRARMGERGRAWVEEKWRWDLLAERLRELL
>NZ_CP019798.1|WP_078094073.1|2468205_2469819_-|GMC-family-oxidoreductase
MTPNLTRRHMLGLGALSTAAALGFTRIGAASAAAVEPAAVPYAPAVVVGSGYGSAVAALRLGQAGVRTVVLEMGRLWDTPGPDGKVFPSTSAPDHRSMWFRTRTEAPLAQFLWLDVVNRDISPYPGVLDRVNFGGMSVYVGRGVGGGSLVNGGMAPTPRRSYFTEVFPGVDADEMYGTYYPRARAMLGVNDIDPAWFESTEWYRFARISRRHAHNTGLKTVFVPNVYDFGHMKREAAGTAPRSALAGEVIYGNNHGKKSVDKTYLAAAVGTGNVTIETMQRVVGVRPDPAGGYVLTVRTSDVTGKVTQVRELGCRQLFLGAGSLGTTEILLRARETGTLPALSDRVGLGWGPNGNVMTARANHLWDTVGAHQATMPALGIDDWDNAANPVFAEIAPLPMGLEHWISMYLAITRNPERGHFTYDAATDSARLNWRREQNTPAVNAAKNLFDRINRRNFTIYRYDLFGGNRAFADDFTYHPLGGCVLGEATDAYGRAKGYQGLYVVDGSLVPGSLGVNPFLTITALAERNMARILADPR
>NZ_CP019798.1|WP_030850108.1|2466363_2468160_+|long-chain-fatty-acid--CoA-ligase
MREFSLPALYEVPSDGNLTDLIRRNAAQHPDTAVMSRKADGRWQDVTATEFLAEVRATAKGLIAAGVRPGDRVALISRTRYEWVLIDFAIWSAGGVTVPVYETSSPEQIQWILGDSGAVAVVVESAAHGEAVASLRDRLPELREVWEIEQGAVQALKAAGAAVTDAEVEERSSLANADDPATIVYTSGTTGRPKGCVLTHRNFFAECGNAVERLSPLFRTGECSVLLFLPAAHVFGRLVEVAAVLAPIRLGCVPDIKNLTDELQSFRPTLILGVPRVFEKVYNSARAKAQAEGKGKIFDAAADTAIAYSRALDTPRGPSFGLKLKHKVFSKLVYSKLHAVLGGRGEYAISGGAPLGERLGHFFRGIGFTVLEGYGLTESCAATTFNPWDKQKIGTVGQPMPGSVVRIADDGEVLLHGEQIFTGYWNNEAATAEALTDGWFHTGDVGTLDEDGYLTITGRKKELIVTAGGKNVAPAVIEDRIRAHALVAECMVVGDARPFVAALVTIDEEFLGRWAAENGKPAGVTAAELREDEDLIAAVQKAIDDGNAAVSKAESVRKFRILPSQFTEESGHITPSLKLKRNVVAKDYADEIEALYRG
>NZ_CP019798.1|WP_078094076.1|2478871_2480287_-|aminotransferase-class-V-fold-PLP-dependent-enzyme
MSASLNTATATAQDPACAEPLAVLGRDVTVPLVTGGEVTYAALDYAASAPALQRVWDDVAAYAPYYGSVHRGAGYLSQLSTDLFEQSRATVAEFLDCRPGDQVVFTRSTTDSLNLLAAVLPADCQVFVFETEHHASLLPWTNAQVSYLNAPRTPGEAVATLERALADRTASIEEGHGPALVCVTGASNVTGELWPVKELAAAAHAHGARIVLDAAQLAPHHPVSVRDLDVDWVAFSGHKLYAPFGSGVLAGRADWLQEAEPYLAGGGASRKVSRREDGGVDVEWHTTAARHEAGSPNVIGVYSIASACRALTEAGFDSLVAREQHLVAKIREGLAEVPAVRVLSLFGDDAPRVGVISFVVDGWNSSHFAAALSAEYGIGVRDGLFCAHPLVRTLLGSEPQAQGECGAPEAAPGERSLNAIRVSFGAGTPDEHVERFVRAVKELVADGAKWQYRTEEGRCVPTAPLRGCSAV
>NZ_CP019798.1|WP_030849374.1|2480713_2481778_-|anthranilate-phosphoribosyltransferase
MNVATPAGGDSVAARGWPGVLDALLTGQDLRADDTAWAMDRIMRGEATDAQIAGFVVALRAKGETVAEINGLVQAMYGHANLIEVPGRTVDIVGTGGDGAKTVNISTMSAIVVAGTGAKVVKHGNRAASSASGSSDVLEKLGVNLDLSTARVVEVAEEAGITFCFAVKFHPALRHVAGARRELGIRTTFNILGPLTNPARVRSQATGVADPRMAPIVAGVLAERGSSALVFRGDDGLDELTTTATSRVWWVRDGKVAEQSFDPRDVGIPLVDVSALAGGDPSYNADVARRLLAGETGPVRDAVLLNSAAALVALDPGTGTLEEQIAAGITRAAESIDSGAARAALERWVTASNA
>NZ_CP019798.1|WP_060178189.1|2481941_2483570_-|ubiquinol-cytochrome-c-reductase-cytochrome-b-subunit
MSTATDNKARKAPAGERVADWADGRLGIYSLAKANMRKIFPDHWSFMLGEICLYSFIIIILTGVYLTLFFHPSMNEVEYHGSYVPMQGVLMSEAFASTLDISFDVRGGLLIRQIHHWAALIFVAAMIVHMMRVFFTGAFRKPREVNWIFGFLLLVLGMFTGFTGYSLPDDLLSGTGVRFMQGAILSVPVVGTYLSMFLFGGEFPGGDFVARFYSVHILLLPGIMMGLLVAHLILVFYHKHTQYAGPGKTNNNVVGMPLLPVYMAKAGGFFFLVFGVISVVAAVASINPIWALGPYRPDHVSTGAQPDWYMGMPEGLIRAMPGWEINLWGHTLVLGVFIPLVLFPLVLGAIAVWPFIESWVTGDKREHHILDRPRNVPTRTAFGVAWIAEYIVLLIGGGNDMFAQYFHLSINSITWFVRIGFFAVPVIAFIVTKRICLGLQRRDRDKVLHGRETGIIKRLPHGEFVEVHEPLPQGKLHTLTAHEQYKPIEIGPTVDENGVERKVKATEKLRAKLSKGFYAEGNQIPKPTVEEYKEIQSGHGHH
>NZ_CP019798.1|WP_030849368.1|2483566_2484625_-|Rieske-2Fe-2S-domain-containing-protein
MSSQEIPEEKHLPSEQGDVHHGGVAVADDPFADPGLPVHKPRIQDIDERAAKRSERTVAMLFTLSMLATIGFIASYVIFPVDKIVFIFPLGKVSALNFALGMTLGTALFCIGAGAVHWARTLMSDVEVADDRHEIAASPEVKAKVLQDFADGANESGIGRRPLIRNTMLGALAMLPLSAVVIMRDLGPLPEDKLRKTLWAKGKLLINQNTMEPLRPEDVLVGSLTFAMPEGLDEHQHDFQVQIAKAALMIVRIQPEDIKDKKELEWSHDGIVAYSKICTHVGCPISLYEQQTHHVLCPCHQSTFDLSDGARVIFGPAGHALPQLRIGVNDEGFLEALGDFEEPVGPAFWERG
>NZ_CP019798.1|WP_030036316.1|2484621_2485431_-|c-type-cytochrome
MKKLSARRRHPLAAVVVLLLALAATGGLYAAFAPAGKAQADETAQSLAIEEGKKLYAVGCASCHGTGGQGSSDGPSLVGVGSAAVDFQVSTGRMPAQQPGAQVPKKPVIYTQAQIDQLAAYIASLGAGPITPTEKQYDPADADIANGGELFRNNCAQCHNFTGEGGALTNGKYAPNLEDVSPKHIYEAMQTGPQNMPSFPDSTMPEKQKKDIIAYLQNVNGEKSTNPGGLKLGGLGPVSEGLFGWIFALGALIAVAVWVAAHTAKAKKS
>NZ_CP019798.1|WP_030849365.1|2485507_2486128_-|heme-copper-oxidase-subunit-III
MSVVATATTVDTGHAHPTVNRPNLVSVGTIIWLSSELMFFAALFAMYFTLRSVTGPEYWTEQANTLNLPFSATNTTILVLSSLTCQLGVFAAERGDVKKLRTWFIITFVMGAIFIGGQVFEYTELVKHEGMSLSSGPYGSVFYLTTGFHGLHVTGGLIAFLLVLGRTYAAKRFTHEQATSAIVVSYYWHFVDVVWIGLFATIYLIK
>NZ_CP019798.1|WP_078094077.1|2486327_2486732_+|hypothetical-protein
MRATARVLVYSDDAGTREQVRLAAGRRPAADLPPVEFLECATLPAVLSALDAGGIDVCVLDGEAVPAGGMGVCRQIKDEIFRCPPVLLLMGRPQDAWLATWSRADAAVTLPVDPVEFADTLAGLLRSRLSSSAA
>NZ_CP019798.1|WP_078094078.1|2486776_2488021_-|L,D-transpeptidase-family-protein
MKHSPRLWTVLSCSLLVASLGAGATACGSGDNPLSARPVDAGEQVAFNQTAGSRPVDPNRPLEITAKAKGSRITDVTAVDIHGRRLAGELSAKGDRWHSTVPMAAGVRYTVTVSTEDERGTPGQRTMAFDTTPSKGVLKVEFGPEEGKYGVGQPLTAELNEPVKDKAARAVVERGLIVDAPPGVEGAWHWVDDKNLHYRPKDYWPANTTVSVRSNLEGIKITDDLHGAAAKPLKLEIGDRVEVTTDAAAHWLTFKRNGEVINSIPVTTGKPGFSTRNGIKVVLGKQYYVQMRGDTVGIGGSEYYNLPVYYATRVTWSGEYVHAAPWSIGSHGYANVSHGCTGMSTGNAAWFYENITEGDIVQVINSIGDDMDIFGNGFGDWNMDWKDWREGSALLKGTQEGRSHIDQARLRPTV
>NZ_CP019798.1|WP_030849356.1|2488152_2488551_-|cytochrome-c-oxidase-subunit-4
MKIQGKMFLWLSFFILIMAVVYGVWSKEPVGTTALFLAFGLSVMIGYYLAFTAKRVDEMAQDNLEADVADEAGELGFFSPHSWQPLSLGIGGALAFMGVIFGWWLMYFSAPIILIGLWGWVYEYYRGENANQ
>NZ_CP019798.1|WP_060178191.1|2488547_2490278_-|cytochrome-c-oxidase-subunit-I
MSILNESQGAAAADSYENELPVRRKQPGNVVVKWLTTTDHKTIGTMYLVTSFVFFIIGGLLALFMRAELARPGTQIMSNEQFNQAFTMHGTIMLLMFATPLFAGFANWIMPLQIGAPDVAFPRLNMFAYWLYLFGSTIAVAGFVTPNGAADFGWFAYSPLSDAVRSPGIGADMWIMGLAFSGFGTILGSVNFITTIICMRAPGMTMFRMPIFTWNVLLTGVLVLLAFPVLAAALFALESDRKFGSHIFDSANGGALLWQHLFWFFGHPEVYIIALPFFGIVSEIIPVFSRKPMFGYIGLIAATIAIAGLSVTVWAHHMYVTGGVLLPFFSFMTFLIAVPTGVKFFNWIGTMWKGSLSFETPMLWTIGFLVTFTFGGLTGVILASPPMDFHVSDSYFVVAHFHYVVFGTVVFAMFAGFHFWWPKFTGKMLDERLGKITFWTLFIGFHGTFLVQHWLGAEGMPRRYADYLAADGFTTLNTISTISSFVLGLSMLPFIYNVWKTAKYGKKIEVDDPWGYGRSLEWATSCPPPRHNFLTLPRIRSESPAFDLHHPEIAALDHLEDHGAKAAVTGGKEAGK

Crispr_ID: NZ_CP019798_6

• CRISPR_ID: NZ_CP019798_6
• CRISPR_location: 2634644-2634753
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_6

Consensus_repeat	Method
GCCCCCGGCACGGGAACCGCAGGCGG	CRISPRCasFinder

spacers of NZ_CP019798_6

>6.1|2634670|58|NZ_CP019798|CRISPRCasFinder
CGGCACGGGAACCGCAGGCGGCCCGGCCGCAGCCGCCGCCCACCCCGCCAAAGCCACC

CRISPR arrays and Neighbor proteins around NZ_CP019798_6

CRISPR arrays

The CRISPR arrays of NZ_CP019798_6

>merge|NZ_CP019798|6|2634644-2634753|CRISPRCasFinder
GCCCCCGGCACGGAAGCCGCTGCCCCCGGCACGGGAACCGCAGGCGGCCCGGCCGCAGCCGCCGCCCACCCCGCCAAAGCCACCGCCCCCGGCACGGGAACCGCAGGCGG

>NZ_CP019798|6|3|2634644-2634753|CRISPRCasFinder
GCCCCCGGCACGGAAGCCGCTGCCCC	CGGCACGGGAACCGCAGGCGGCCCGGCCGCAGCCGCCGCCCACCCCGCCAAAGCCACC
GCCCCCGGCACGGGAACCGCAGGCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078094139.1|2642770_2643439_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379883
NZ_CP019798.1|WP_078094138.1|2640762_2641785_+|rRNA-methyltransferase	unknown	unknown	gnl|CDD|286344
NZ_CP019798.1|WP_030848998.1|2643552_2644302_+|bifunctional-DNA-primase/polymerase	unknown	unknown	gnl|CDD|378140
NZ_CP019798.1|WP_076045302.1|2641781_2642612_-|amidinotransferase	unknown	unknown	gnl|CDD|224747
NZ_CP019798.1|WP_107052327.1|2629364_2630030_-|PhzF-family-phenazine-biosynthesis-protein	unknown	unknown	gnl|CDD|223461
NZ_CP019798.1|WP_173675220.1|2638478_2639351_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|212491
NZ_CP019798.1|WP_078094131.1|2631542_2633468_-|HtaA-domain-containing-protein	unknown	unknown	gnl|CDD|367875
NZ_CP019798.1|WP_078094140.1|2644342_2645146_-|peroxide-stress-protein-YaaA	unknown	unknown	gnl|CDD|234999
NZ_CP019798.1|WP_078096181.1|2635857_2636727_+|heme-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|237422
NZ_CP019798.1|WP_107499869.1|2639328_2640669_+|Bcr/CflA-family-multidrug-efflux-MFS-transporter	unknown	unknown	gnl|CDD|340878
NZ_CP019798.1|WP_078094129.1|2628651_2629299_+|biliverdin-producing-heme-oxygenase	unknown	unknown	gnl|CDD|350856
NZ_CP019798.1|WP_078094135.1|2637560_2638424_-|PhzF-family-phenazine-biosynthesis-isomerase	unknown	unknown	gnl|CDD|223461
NZ_CP019798.1|WP_030849045.1|2625896_2626601_-|NADPH-dependent-F420-reductase	unknown	unknown	gnl|CDD|273873
NZ_CP019798.1|WP_078094134.1|2636899_2637475_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|225064
NZ_CP019798.1|WP_078094128.1|2627312_2627570_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030849038.1|2627663_2628521_+|type-I-methionyl-aminopeptidase	unknown	unknown	gnl|CDD|235576
NZ_CP019798.1|WP_030849042.1|2626685_2627294_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094132.1|2633583_2634600_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|238569
NZ_CP019798.1|WP_030849047.1|2625609_2625798_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094130.1|2630049_2631492_-|HtaA-domain-containing-protein	unknown	unknown	gnl|CDD|367875

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_078094139.1|2642770_2643439_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	5.25094e-26
NZ_CP019798.1|WP_030848998.1|2643552_2644302_+|bifunctional-DNA-primase/polymerase	gnl|CDD|378140	pfam09250, Prim-Pol, Bifunctional DNA primase/polymerase, N-terminal. Members of this family adopt a structure consisting of a core of antiparallel beta sheets. They are found in various bacterial hypothetical proteins, and have been shown to harbour both primase and polymerase activities.	2.17405e-21
NZ_CP019798.1|WP_076045302.1|2641781_2642612_-|amidinotransferase	gnl|CDD|224747	COG1834, COG1834, N-Dimethylarginine dimethylaminohydrolase [Amino acid transport and metabolism].	6.0379e-61
NZ_CP019798.1|WP_107052327.1|2629364_2630030_-|PhzF-family-phenazine-biosynthesis-protein	gnl|CDD|223461	COG0384, COG0384, Predicted epimerase, PhzC/PhzF homolog [General function prediction only].	2.25527e-15
NZ_CP019798.1|WP_173675220.1|2638478_2639351_-|SDR-family-oxidoreductase	gnl|CDD|212491	cd05233, SDR_c, classical (c) SDRs. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.79055e-64
NZ_CP019798.1|WP_078094131.1|2631542_2633468_-|HtaA-domain-containing-protein	gnl|CDD|367875	pfam04213, HtaA, Htaa. This domain is found in HtaA, a secreted protein implicated in iron acquisition and transport.	2.83663e-51
NZ_CP019798.1|WP_078094140.1|2644342_2645146_-|peroxide-stress-protein-YaaA	gnl|CDD|234999	PRK02101, PRK02101, peroxide stress protein YaaA.	1.48545e-68
NZ_CP019798.1|WP_078096181.1|2635857_2636727_+|heme-ABC-transporter-ATP-binding-protein	gnl|CDD|237422	PRK13548, hmuV, hemin importer ATP-binding subunit; Provisional.	9.8581e-120
NZ_CP019798.1|WP_078094129.1|2628651_2629299_+|biliverdin-producing-heme-oxygenase	gnl|CDD|350856	cd19165, HemeO, heme oxygenase in eukaryotes and some bacteria. This subfamily contains heme oxygenase (HO, EC 1.14.14.18) found in eukaryotes as well as some proteobacteria, including cyanobacteria. Heme oxygenase (HO) catalyzes the rate limiting step in the degradation of heme to biliverdin in a multi-step reaction. HO is essential for recycling of iron from heme which is used as a substrate and cofactor for its own degradation to biliverdin, iron, and carbon monoxide. In vertebrates, HO plays a role in heme homeostasis and oxidative stress response, and cellular signaling in mammals that include isoforms HO-1, HO-2 and HO-3. HO-1 is ubiquitously expressed after induction while HO-2 expression is constitutive, mostly limited to certain organs, such as the brain, testes, and the vascular system. HO-3 is non-functional in humans, suggesting that the Hmox3 gene is a pseudogene derived from HO-2 transcripts. In higher plants and cyanobacteria, heme oxygenase is required for the synthesis of light-harvesting pigments, which contain tetrapyrrols derived from biliverdin. Candida albicans expresses a heme oxygenase that is required for the utilization of heme as a nutritional iron source, whereas Saccharomyces cerevisiae responds to iron deprivation by increasing Hmx1p transcription, which is controlled by the major iron-dependent transcription factor, Aft1p, and promotes both the re-utilization of heme iron and the regulation of heme-dependent transcription during periods of iron scarcity. In pathogenic bacteria, HO is part of a pathway for iron acquisition from host heme. In Leptospira interrogans, a pathogenic spirochete that causes leptospirosis, HO is required for iron utilization when hemoglobin is the sole iron source, thus making HO an interesting target for novel antimicrobial agents. HO shares tertiary structure similarity to methane monooxygenase (EC 1.14.13.25), ribonucleotide reductase (EC 1.17.4.1) and thiaminase II (EC 3.5.99.2), but shares little sequence homology.	1.31887e-79
NZ_CP019798.1|WP_078094138.1|2640762_2641785_+|rRNA-methyltransferase	gnl|CDD|286344	pfam09243, Rsm22, Mitochondrial small ribosomal subunit Rsm22. Rsm22 has been identified as a mitochondrial small ribosomal subunit and is a methyltransferase. In Schizosaccharomyces pombe, Rsm22 is tandemly fused to Cox11 (a factor required for copper insertion into cytochrome oxidase) and the two proteins are proteolytically cleaved after import into the mitochondria.	3.9031e-119
NZ_CP019798.1|WP_030849045.1|2625896_2626601_-|NADPH-dependent-F420-reductase	gnl|CDD|273873	TIGR01915, F420-dependent_NADP_reductase, NADPH-dependent F420 reductase. This model represents a subset of a parent family described by pfam03807. Unlike the parent family, members of this family are found only in species with evidence of coenzyme F420. All members of this family are believed to act as NADPH-dependent F420 reductase. [Energy metabolism, Electron transport].	1.27923e-77
NZ_CP019798.1|WP_078094134.1|2636899_2637475_-|GNAT-family-N-acetyltransferase	gnl|CDD|225064	COG2153, ElaA, Predicted acyltransferase [General function prediction only].	0.000104483
NZ_CP019798.1|WP_030849038.1|2627663_2628521_+|type-I-methionyl-aminopeptidase	gnl|CDD|235576	PRK05716, PRK05716, methionine aminopeptidase; Validated.	8.84538e-145
NZ_CP019798.1|WP_107499869.1|2639328_2640669_+|Bcr/CflA-family-multidrug-efflux-MFS-transporter	gnl|CDD|340878	cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.78866e-111
NZ_CP019798.1|WP_078094132.1|2633583_2634600_+|ABC-transporter-substrate-binding-protein	gnl|CDD|238569	cd01149, HutB, Hemin binding protein HutB. These proteins have been shown to function as initial receptors in ABC transport of hemin and hemoproteins in many eubacterial species. They belong to the TroA superfamily of periplasmic metal binding proteins that share a distinct fold and ligand binding mechanism. A typical TroA protein is comprised of two globular subdomains connected by a single helix and can bind the metal ion in the cleft between these domains.	1.06607e-76
NZ_CP019798.1|WP_078094135.1|2637560_2638424_-|PhzF-family-phenazine-biosynthesis-isomerase	gnl|CDD|223461	COG0384, COG0384, Predicted epimerase, PhzC/PhzF homolog [General function prediction only].	5.13278e-71
NZ_CP019798.1|WP_078094130.1|2630049_2631492_-|HtaA-domain-containing-protein	gnl|CDD|367875	pfam04213, HtaA, Htaa. This domain is found in HtaA, a secreted protein implicated in iron acquisition and transport.	1.02004e-34

Protein sequences

>NZ_CP019798.1|WP_078094132.1|2633583_2634600_+|ABC-transporter-substrate-binding-protein
MPTPAASHRFPRLAVAVTALALALALTGCGGTATPPGSPAPAAAAPDRVEPLAATPQPALPVTVPSADGAQVTVTSADRVIPLTGSLNEIVHTLGLGGQVVARDITATFEQAARLPVVTRGHDVSAESVLSLRPTLVLAETTTGPAEAVQQIRDAGIPVLVVAPAKGLDDVPKRIDAVAAALGVKDAGAQLTRRTADRIAAVRKNVPASGGKQPRVAFLYLRGTASVYLLGGSDSGAASLLEAAGAVDTGKESGLGKDFTPITSEALAAAAPDAILVMSKGLESVGGIDGLVKIPGVAQTPAGMDRRVVTVDDGVLLNYGPRTDQVLSSLITQLYGKG
>NZ_CP019798.1|WP_078094131.1|2631542_2633468_-|HtaA-domain-containing-protein
MPARPVRTLAIALLAGLLGALLPATAAHAGTVQGGRLDWGIKSSFQSYVTGPVAKGGFQLKGGAATAGGSLFRFHSATGSYDPDTGAFEASYSGGVTFQGHQKPDGVHELDMTVSRPTVKISGGSGTLYVDVSSRAKDTGAVSNQSQVPFATLGVGGINMKGGASPLTLTGIPATLTSQGAQAFAGYYPAGTRLDPLSLSADVKTAPAGEVSQPATAQPGATAEAPQAPGAFADAAVDWGVRRTFREYVTGSVGQGKWTLAEGAQDGGALFRFPQGKGAYDGRKGTLDAAFAGTVQFTGAHLDLTLGKVGVKVENGKGVLSADVTTQGATKNAVPLVEFDAKALKAEGALVTLTEAPATLTEGGSQAFNSMYKAGTEMDPVSLAVALDATAKLPALPDLGSTASPSAAPAPAPSADEPAPAAESGTSSNTGLYAALAAAALLLAVAAALLLRKRRPNPAATATATPSPGPASGSAQASAAGSVAPAPAPASGSAQAADAASGQVPTPGSAASAASSASGSPASGSVPASAAGSVAPTASAASAAPAPASGSAQAADAASGQASTPGSAASAAGPSAGRGPTPAAGSGAASAPAPAPAPASASAQAGPSAGTAPGNGSGSGSAAEASAGAARSSEPDADGVK
>NZ_CP019798.1|WP_078094130.1|2630049_2631492_-|HtaA-domain-containing-protein
MSSIRRPISLAAAVLTAAALGTTAFSLPATAAGGPPTGPVKIVGGTLDWGVLAGYRAYVTGMAKGTITVAEGAQQNADGTLRFIEATGQYDPAGGHVVKAAFKGSVTFSSPAPPTGHGFEVKLSDIRIDTGTKKLTADVTKSGATAQDVPLATVAFAGPSMTGLATTLTKEAADALGSPGYENKAGDPLTAHLKFEEPAPEPTPTKPTPTKDPPPTKDPAPTQDPQPTTPADGTQKVLNGKLTWGVKESFRRYVLGAGSITPAGGAAKNGELFDFAFGKGELDVKKQKLNASFEGTLRFQYAAHGIDMTFGNPRIDATGKTGTLYVDVKNAAGSRTGVAFATLDLSKTDYKTQHGVLALNGVPAAFTADGAAAFANDTTGPMYRAGDPIDPVTFSVAVDKDATLPPSTGGTTTGGSAGTTTGGSAGTAGGGSVGGASVGGNLADTGAEIPAAALLTTSGVVIAAGAGAVHLARRRRTAQL
>NZ_CP019798.1|WP_107052327.1|2629364_2630030_-|PhzF-family-phenazine-biosynthesis-protein
MNDLDVLKVFCAGDGRHGNLLGVVRDGRTCPDDASRQALAAELGYSETVFVDDPERGVVDIRTPGTRMSFAGHPLVGVAWLLDIEELQPPVGSVWARDDGEFTWITARPEWVEGKRTQQYASVAEVEALPAPPPGEGWLYAWAWEDEAAGRVRARGFPRRPDGVIAEDEATGSAAILLTAQLDRALNITQGAGSQILTAPGADGTIEVGGRVRFAPPAHPA
>NZ_CP019798.1|WP_078094129.1|2628651_2629299_+|biliverdin-producing-heme-oxygenase
MDAFSTVIRVASHEQHTEAETSTFMSDLLGGRLGVDAYTRYTEQLWFVYRALEEAAESLKDDPVAGPFIRPELMRVAEIERDLAHLLGPQWRRNVVALPSTEAYAARVAQCAAEWPGGYVAHHYTRYLGDLSGGQIIRDKAERTWGFERKGDGVRFYVFADISNPAAFKRTYRELLDAIAADDLEKQRIIDECKRAFDFNGAVFRELGEEFRLSA
>NZ_CP019798.1|WP_030849038.1|2627663_2628521_+|type-I-methionyl-aminopeptidase
MSGQSLLVPGELSPARSVPGNIRRPEYVGKPAPTPYTGPEVQSAETIEAMRIAGRIAAQAMEEAAKLIAPGVTTDELDRVAHEYMCDHGAYPSTLGYRGYPKSLCSSVNEVICHGIPDSTVLRDGDIVNLDVTAYIGGVHGDNNATYLCGDVDEESRLLVERTREALNRAIKAVKPGRQINVIGRVIESYAKRFGYGVVRDFTGHGINSSFHSGLIIPHYDSPHATTVIEPGMTFTIEPMLTLGTHDYDMWDDGWTVVTKDRKRTAQFEHTLVVTDSGADILTLP
>NZ_CP019798.1|WP_078094128.1|2627312_2627570_-|hypothetical-protein
MALFKKRQVGKPGEWYYCLVHQKVEEGPECPAKDRFGPYGTPEEAAHAMETAQERNLEWQNDPKWNDKTREEEEGTSGTGTGTSG
>NZ_CP019798.1|WP_030849042.1|2626685_2627294_+|hypothetical-protein
MDAVRVALLREVLAGTQWPGDARRFAGSLRRSVAPAGGKLLLVGTEGYEPWHMAAHLVDEAAWSGLPELAPTLVRHRVRPGEPPHLSVGLGRLAAAGRGHTVLVVAPREPGEGLLERVYDARRAGATVLSLDGGDRDLGALAHDALSVPDGAAELDLDTVQHLVSAAAGENGPPAQRGARRRLRDRLAGLADRLTAPPPSRW
>NZ_CP019798.1|WP_030849045.1|2625896_2626601_-|NADPH-dependent-F420-reductase
MTSSDNPQKPQAKDPWDLPDVSGLVVGVLGGTGDQGRGLAYRLARAGQKVIIGSRAADRARTAAEELGLGVEGADNAECARRSDIVIIAVPWEGHAKTLEALREDLAGKLVVDCVNPLGFDKQGAYALQVEEGSAAQQAAALLPDSRVTAAFHHLSAVLLQDASIDEIDTDVMVLGESRADTDIVQALAARIPGMRGIFAGRLRNAHQVEALVANLISTNRRYKAHAGLRTTDV
>NZ_CP019798.1|WP_030849047.1|2625609_2625798_-|hypothetical-protein
MPRLAVFAVVVCVLAVAAAVVAFVEGSFLGIVWVLLAGLTSNMAWYYMRKAKAEKAATARNA
>NZ_CP019798.1|WP_078096181.1|2635857_2636727_+|heme-ABC-transporter-ATP-binding-protein
MARLFARGRRTVPARPAPGTALAEAVDLHVRLGQREVLAGIDLSARAGEVLALVGPNGAGKSTLLAALAADLPAASGEVRIHGRPVGDWSAPDLALRRSVLPQAAALSFPFPVEDVVRMGRAPWAGTPFAEADEEAVAAAMAAAEVGEFAARPFSALSGGERARVALARVLAQRAPLLLLDEPTAALDLRHQELVLRICRERARAGDAVVVVLHDLGLAAAYADRAAVLHDGRIAADGPPAEVFEDALLSRVYRQPVEVLPHPRTGAPLVVPVRAVEGSYDGLVSQAGT
>NZ_CP019798.1|WP_078094134.1|2636899_2637475_-|GNAT-family-N-acetyltransferase
MSAEPRVLGFAEADVPAALAVQVTDLEAEAWPGSTPGHDPALAPRTLLLLDDEGAVAAALALLYKGIPLAGRTYRAAGLSSVVTRSALRGQGFGGRLVAAARAELAADPAVDLALFSCDRPLAPFYEAAGFAPLPGTVLVGGTPGDPLATDAPGFDKVVMAAFFTETPAADRAAFTAVRVPLHPGSVDRLW
>NZ_CP019798.1|WP_078094135.1|2637560_2638424_-|PhzF-family-phenazine-biosynthesis-isomerase
MTDTEVLRYTAFSDDPDGGNPAGVVLDASGLDEDAMLEIAATLGYSETAFLTDPPEGLGGQEGRSFTVRYFSPKAEVPFCGHATVATAVALAERIGAGELLLATRAGTVPVSVTAEHGRLRATLTSVEPHIEEIAAADLAEALAALEWPQADLDPAFPPRIAYAGARHLVIGAATRARLADLDYDFARLEALMRRLDLTTVQLVHREGPREFHVRDPFPVGGVVEDPATGAAAAAFGAYARALGLVPQDAVLTLHQGADMGRPGVLTVELREGDPRVRVGGAAVRIP
>NZ_CP019798.1|WP_173675220.1|2638478_2639351_-|SDR-family-oxidoreductase
MQNSSLLICSYAPLTDPCSQQSERPGTGARCDVPCGPMDEPTKKIAVVTGAGSGIGRSVALTLAAAGWAVALAGRRAEPLQETAAAAGADADVLCVPADVSDPDEVNRLFESVRARYGRLDLLFNNAGTFGPAGVPLEDITYEAWRSVVDVNLTGAFLCAQAAFRQMKGQDPQGGRIVNNGSISAHVPRPNSIAYTATKHAMTGLTKSLSLDGRPYRIACGQIDIGNAATEMTERMQAGILQANGQLAVEPVMDAADVARTVLHMAELPLEANVQFATVMATAMPYIGRG
>NZ_CP019798.1|WP_107499869.1|2639328_2640669_+|Bcr/CflA-family-multidrug-efflux-MFS-transporter
MRRLEFCMSERGPATAPSHDSSPESPSAPSATASLTRARRTSLLVTFILGGLTALPPLSMDMYLPALPQVTDALNSPAATIQLTLTACLAGMALGQLVIGPMSDKWGRRRPLLVGMVVYVLATAICALAPTAELLIAFRLLQGLAGAAGVVIARAVVRDLYDGDEMARFFSTLMLISGAAPIVAPLIGGQVLRFADWRGVFVVLTGVGMLLTLMVWRGLGETLPPERRHTGGVGSALRTMRGLLGDRVFTGYTLTGGFAFAVLFAYISASPFVVQEIYGASPQTFSLLFGLNSVGLILVGQVNGKLLVGRVRLDKVLAVGLAVVLASAVSLLLMATGAFGEVGLAPIAGALFVLMSAMGIVLPNTNAQALMRTPHAAGSASALLGTSSFLVGAIASPLVGIAGEDTAVPMALVQLVCAVLSVSCFLALCRPWQKRDAQTAPAAAED
>NZ_CP019798.1|WP_078094138.1|2640762_2641785_+|rRNA-methyltransferase
MNLSAPTTADTLRSTLGGLLDGLPPKQASAAVERLIANYRGRTPTDAPVLRDRSDVAAYAAYRMPATFEAVRAALDALAEAAPDWAPASHVDVGGGTGAATWAVDATWDGPRQTTVLDWAEPALALGRELAAASGSPVLRGAEWRRAVIGSGMAIPDADLVTVSYVLGELTPQARTAVVAEAARAGRAVVLIEPGTPEGYLRIREARDQLIAAGLKVAAPCPHDGTCPIEVGKDWCHFSARVSRSSLHRQVKGGSLPYEDEKFSYVAATRFPVEPAASRITRKPQIRKGLVLLELCGPEEGDGAGLTRVNVTKRHGDLYKAARDADWGRAWPPPSGDTGN
>NZ_CP019798.1|WP_076045302.1|2641781_2642612_-|amidinotransferase
MRRDATPRRYLMCPPAHFKVTYSINPWMDPTKPVDLPLAQTQWEDLRDRYVSLGHTVETLVPDPELPDMVFAANGALVVDGRVLGARFAHPERAAEAGRHLDWFRSHGYRDIREPAHVNEGEGDFAVTASFILAGRGFRSSPLSHDEAQEFFGRPVIGLDLVDPRYYHLDTALSVLDGDEVMYYPEAFSPGSRGVLRRLFPDALIADGRDAAALGLNAVSDGRHVLLPQAATGLFGPLRERGFEPIPMDLGELLKGGGSVKCCTQELRPGPGLGAA
>NZ_CP019798.1|WP_078094139.1|2642770_2643439_+|TetR/AcrR-family-transcriptional-regulator
MTRTPDATRRSDRSRRAILDAALALVGEVGYNKLTIEAIAARAGVGKQTIYRWWPSKAAVLLEASLALAGDAEADAEWAGFPDTGDLAADLKFVLRATVDEFNDEKYEAPARALTAAGATDPELGARFTEQLLEPQLALYEARLRTAREAGQLAPDTDLRLTVEMLLGPLTYRWLLRTAPLTHAYTDALVDRVLGGVANVTARQAADHLRSPRNVCPDSAGM
>NZ_CP019798.1|WP_030848998.1|2643552_2644302_+|bifunctional-DNA-primase/polymerase
MGSESGRVERGEQSRISQWLRRRQKPTAEDPAREREALLLAVAAAGLPLAPAAHPVGYRCSCDRIGCPTPARHPVSFAWQTQSTTDRAQIERWARNQPQANFITATGMVHDVLDVPLEAGAAALTRLLEAGIKVGPVAESAGTGDQARMLFFTATRGTPEDEDEWWPCALDCHPETMDEHPGLRWHCRGSYVLVPPAALPGDQAVTWIRGMEHPLPDPLTLLETLTDACAAYADTSDRTPATVAWPLGR
>NZ_CP019798.1|WP_078094140.1|2644342_2645146_-|peroxide-stress-protein-YaaA
MLVLLPPSEGKAAGGSGAPLEPQELSLPGLAPARAAVLEELLDLCTGDELKAREVLGLSEGLRGEVAKNAELRSAAARPAGEIYTGVLYDALGLADLPAPARIVAEDALLVFSGLWGAVRVTDRIPSYRCSMGVKLPGLGALGAYWRAPMAEVLPAAAGDGLVLDLRSAAYATAWKPKGEVAGRTATVRVLHSQMVDGVEKRSVVSHFNKATKGRLVRDLLVAGAVPGSPAELVTALRDLGYVVEAQAPAKAGRAWSLDVVVTQIHH

Crispr_ID: NZ_CP019798_7

• CRISPR_ID: NZ_CP019798_7
• CRISPR_location: 2792166-2792269
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_7

Consensus_repeat	Method
TGCTCTGCCAATTGAGCTACAGGGGA	CRISPRCasFinder

spacers of NZ_CP019798_7

>7.1|2792192|52|NZ_CP019798|CRISPRCasFinder
CTGCGCTCCCCCGACTGGACTCGAACCAGTAACCTGCCGGTTAACAGCCGGC

CRISPR arrays and Neighbor proteins around NZ_CP019798_7

CRISPR arrays

The CRISPR arrays of NZ_CP019798_7

>merge|NZ_CP019798|7|2792166-2792269|CRISPRCasFinder
TGCTCTGCCAATTGAGCTACAGGGGACTGCGCTCCCCCGACTGGACTCGAACCAGTAACCTGCCGGTTAACAGCCGGCTGCTCTGCCAATTGAGCTACAGGGGA

>NZ_CP019798|7|4|2792166-2792269|CRISPRCasFinder
TGCTCTGCCAATTGAGCTACAGGGGA	CTGCGCTCCCCCGACTGGACTCGAACCAGTAACCTGCCGGTTAACAGCCGGC
TGCTCTGCCAATTGAGCTACAGGGGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_030841089.1|2794400_2796134_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_CP019798.1|WP_060178092.1|2782472_2783630_+|glutamate--cysteine-ligase	unknown	unknown	gnl|CDD|237408
NZ_CP019798.1|WP_078094197.1|2787969_2788161_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030841092.1|2792814_2794263_+|sugar-kinase	unknown	unknown	gnl|CDD|198375
NZ_CP019798.1|WP_159425536.1|2784398_2786096_+|AIPR-family-protein	unknown	unknown	gnl|CDD|378452
NZ_CP019798.1|WP_078094203.1|2799865_2801227_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_173675325.1|2787787_2787973_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030841052.1|2804106_2804877_-|glucose-1-dehydrogenase	unknown	unknown	gnl|CDD|187600
NZ_CP019798.1|WP_078096191.1|2789816_2790512_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_076043593.1|2796130_2798053_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_CP019798.1|WP_078094201.1|2791205_2791553_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_159050726.1|2803886_2804048_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094196.1|2786247_2787477_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224314
NZ_CP019798.1|WP_076043612.1|2801332_2801695_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094199.1|2788842_2789655_+|phosphotransferase	unknown	unknown	gnl|CDD|225714
NZ_CP019798.1|WP_078094204.1|2801746_2803840_-|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl|CDD|239155
NZ_CP019798.1|WP_078094198.1|2788295_2788757_+|hypothetical-protein	unknown	unknown	gnl|CDD|226728
NZ_CP019798.1|WP_030841096.1|2792414_2792720_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094200.1|2790579_2791116_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094202.1|2799422_2799866_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_060178092.1|2782472_2783630_+|glutamate--cysteine-ligase	gnl|CDD|237408	PRK13517, PRK13517, glutamate--cysteine ligase.	4.46648e-119
NZ_CP019798.1|WP_030841089.1|2794400_2796134_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	2.09587e-162
NZ_CP019798.1|WP_030841092.1|2792814_2794263_+|sugar-kinase	gnl|CDD|198375	cd07809, FGGY_D-XK_1, D-xylulose kinases, subgroup 1; members of the FGGY family of carbohydrate kinases. This subgroup is composed of D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17) from bacteria and eukaryota. They share high sequence similarity with Escherichia coli xylulokinase (EcXK), which catalyzes the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. Some uncharacterized sequences are also included in this subfamily. EcXK exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of Mg2+ or Mn2+ might be required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	2.42104e-119
NZ_CP019798.1|WP_078094199.1|2788842_2789655_+|phosphotransferase	gnl|CDD|225714	COG3173, COG3173, Predicted aminoglycoside phosphotransferase [General function prediction only].	0.00199302
NZ_CP019798.1|WP_078094204.1|2801746_2803840_-|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_CP019798.1|WP_078094198.1|2788295_2788757_+|hypothetical-protein	gnl|CDD|226728	COG4278, COG4278, Uncharacterized conserved protein [Function unknown].	8.37294e-11
NZ_CP019798.1|WP_030841052.1|2804106_2804877_-|glucose-1-dehydrogenase	gnl|CDD|187600	cd05341, 3beta-17beta-HSD_like_SDR_c, 3beta17beta hydroxysteroid dehydrogenase-like, classical (c) SDRs. This subgroup includes members identified as 3beta17beta hydroxysteroid dehydrogenase, 20beta hydroxysteroid dehydrogenase, and R-alcohol dehydrogenase. These proteins exhibit the canonical active site tetrad and glycine rich NAD(P)-binding motif of the classical SDRs. 17beta-dehydrogenases are a group of isozymes that catalyze activation and inactivation of estrogen and androgens, and include members of the SDR family. 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.	2.11882e-99
NZ_CP019798.1|WP_078094196.1|2786247_2787477_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224314	COG1396, HipB, Predicted transcriptional regulators [Transcription].	1.20786e-06
NZ_CP019798.1|WP_076043593.1|2796130_2798053_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP019798.1|WP_159425536.1|2784398_2786096_+|AIPR-family-protein	gnl|CDD|378452	pfam10592, AIPR, AIPR protein. This family of proteins was identified in as an abortive infection phage resistance protein often found in restriction modification system operons.	1.7043e-34

Protein sequences

>NZ_CP019798.1|WP_078094201.1|2791205_2791553_-|hypothetical-protein
MPQVVQPHPPQPSALPVGQVRVVLEPDSADQPTEELGGVFRAQGVAVLMGEHEPVVQVRRLPLPALLLPPQLDGAPAEHRAQVEAMRRCAELHTLRLARPMPRDEQGQPLIVRFH
>NZ_CP019798.1|WP_078094200.1|2790579_2791116_-|hypothetical-protein
MYQLDGIEHATNAAAEQIRAYAERMSAPTARDATEQLLAETRRGRAWDRTRALLDAGRSAADVIGSADVDTLRALRVELPSYLAARSSKPEGLAGLGWTEADPDPVLRMVDRALVDRLPKDQSAALRIRLDLDRAELGLRETAAGLRRQVDGSAADGDGLRSALAARFADQEAAQLDA
>NZ_CP019798.1|WP_078096191.1|2789816_2790512_+|hypothetical-protein
MQPRARVGFHGEQQDTSSAGWLRLLALVEEAAADGREEFNPLVELSPQERRDVITLPASIARLTEVKHLRLYGSNLVRIPPEIGAMTNLEEFSPYTSHRLHWFPYEITRCSKLARSTVSTRSLFGNFKYRPPFPRLRTTSEVQSGGHLAALDPKQWGTTAISTCSVCDGPVEGRELHQRWISLVVGTDVLPLLVNACSTACVAALPPGAAKHAPLPHSGGWEAVQPSADWA
>NZ_CP019798.1|WP_078094199.1|2788842_2789655_+|phosphotransferase
MDRTAWLELPPEARSAVETYTGPVEHAETAETGVMARLACTLHTATGPVFVKGTRSDEPTAWMYDYEARVTRVAPLAPRVLWQVDAGGWLLTGYEYLVGPHPDLSPGSPDLGPFLDALTTMSEAPWPEQVRKKPLHIRWSGFLPADHSPDLGGRALVHSDVSPLNMLATGDGIRVLDWALACPGPAWADAAFAIPRFIHAGHTAEQAEALAQAVPAYSKAEPSAVATFAATLCGVWESRAASDPAPHRAPLIAAARAWTMHRSSQHVHSA
>NZ_CP019798.1|WP_078094198.1|2788295_2788757_+|hypothetical-protein
MTVVQERPATDARNLIGAKLRATLVSDMQAKFPELTDDKADRGVGQMLAFLAAGAHSDTPLSPSPLVDDFWHAFLLHTQAYQDFCSGTIGKFVHHQPGFLDKEEHGGGKALRARTVDAIVAAGFVIDMEFWPELDLADCSQCHANCHNSPKYA
>NZ_CP019798.1|WP_078094197.1|2787969_2788161_+|hypothetical-protein
MTARQAAPSGIAGGDPVGRFLSWIWVLGTAAGFAALATTTTAELGHRDALSAMTVPDAGFPAR
>NZ_CP019798.1|WP_173675325.1|2787787_2787973_+|hypothetical-protein
MRRDAVYDHRAQQSALPVLVHYDDGGTAESLLVLTPDQVELYAIQFERLISQREQAQGNAA
>NZ_CP019798.1|WP_078094196.1|2786247_2787477_+|helix-turn-helix-transcriptional-regulator
MLEEAEEIGRRVRRARLRLGMPQADLAAALGKTQGWVSKMERGLIELDRVGLLNLVAAELHVHPNDLIGRPYASSPAENQWQVSAVSILRELRRYDLAPIFDGAPRASGELWRDMTRLHRLRDAAANTAILATLPDLLREARALAEAATGHEREEAFAIYAVACKFAHTAAHALGHPELVAMAAERAAWAARLSADPVMPALADWMRVWDMWATADWDDSLTLSDKAIASVQREYELGEPLALRMWGTLHLRAAVAAARAGRPAEADERINHARAAARRMAGHHNPPIYDRHSVTFSPGNVQIHAISVALETGEQTKALAINRRTTPELVAALPNSRQGHHHMDLARAWLWDGNRDRALTELETAERIAPQLVRNHPIARSTLRGIVYAERIATREKLRRMSDRFHLDG
>NZ_CP019798.1|WP_159425536.1|2784398_2786096_+|AIPR-family-protein
MASNDLVLIDQVLKQRAAESPLLADKIFEVFACEQAITAGDLSLEEIQAGVIGGGGDGAIDGVYVFLNERLLAEEDETPSPADVPRGSRLLLWLVQAKREKSFTETALDLASSSTRRLLDLEESEEDLLELYGADLVNKIARFRQTLTAIVTRNPQVEVRFSYVSRGETAEVNSKVEKKARDLERDFAAKFTGGIGKVEFIGASELWQRSNQVRSYTLELPYTESITHGTSHIALVTLRDYLGFICNDDGTLRRHIFDWNVRDYEGGVEVNREIKESLLDRSAPQFWWLNNGVTITCSRAWTVGGKVFSLDDVQIVNGLQTSHTVHEALRDQDPEHPSFNGLIQVRILNTNNVEERDKVIRATNRQTKVPDASLHATDDNQRKIEAFFLEHDWFYDRRKNYYRNLGKPADRIIGIPLLAQALAAMGFSEPHSARSRPSSLLKSPSNYKKYFSTTTPLPVYLWLARQQRTVDTFLANDVHPSERTDLRFHLAMLSAAQLLGAAVHNPRQLRDLSDQGTHSDEAALTDLLYLLIRERDAYAEASKSSFDKIAKGPNFVPVLLKAAGH
>NZ_CP019798.1|WP_060178092.1|2782472_2783630_+|glutamate--cysteine-ligase
MIEPGNSTTSTGTTQNTVRPTVPLTIGVEEEFLLVDARTLRVVPAAPLVLATAGGLPGEMHPEGTRYQVEISTPIAASAASLRAELAELRRTLGRAARAHGCRLLAAPSPVVAVEGPLHLTDDEPRQREQHRRFGALTDTLVSCGRHIHVGTLDVDTAVAVSNRIRPWLPTLIALAANSPFWGGRDTGHCSWRAMAWSGWPSAGPPPHFTSTAHFRRSVQTLLGSGAALDTKMVYWDLRPSGHWPTLELRAPDMSPDVDSAVLQAELARALVATALREIDERRPEPALRDDVLRLARWRAAHDGLEGFGLDPYTGTELPAADLAEALLDLVAPELAAAGDLDHAAKTLARLLRDGSGAHRQRAAYARRQDLTDVLRHLVDETEDF
>NZ_CP019798.1|WP_030841096.1|2792414_2792720_+|hypothetical-protein
MRYKVTFVVGLALGYVLGTRAGRERYEQLKKSARQIAQNPAVRNAAETAGHTGREYAGKAFAAVSEKVGDAVPDSLAERVRGLRGRTGGQAGDDEWGTSNT
>NZ_CP019798.1|WP_030841092.1|2792814_2794263_+|sugar-kinase
MGIVAGLDSSSAFTRIVVCDAETGAVLRQGYAPHPQPVGEPDGANPHETDPQAWLLSLGEAAGGGILEGVQAIGVSAQQHGLLPLDPQGALVRPALVGNDKRGQVAAADLTEALGGRHAWAEAVGSVPHSAQPVAKLAWLARTEPEAARRVAVLMSPHDWLVWQLLGRPARRTTDRGGASGTGYWSAASGAWRPDLVELALGHRALLPEVLGPADAAGTTPEGLLISAGTGETMAAALGLGLGPGDAVVSLGASGSVMAVHHEALSEPGGLITSLADATGMHLPVVNTSNAVRALRGTAELLGTDLEGLSELALKSTPGAHGLVLLPYLEGERTPNLPHSAGTLTGLRRDSMKPEHLARAAFEGMLCGLVDALDVLRSRGVEIRRVFLLGAAAELPAVQAAAPGLFGTQIVVPAPADYAALGAARQAAWALGAAQGTLAPHTPPVWPAPAALVFEPGEDFPAWQGVRQQYIATREQIHPGAF
>NZ_CP019798.1|WP_030841089.1|2794400_2796134_+|ABC-transporter-ATP-binding-protein
MLIRLLRTHLGPYRKPVAALVLLQLLQTSASLYLPTLNADIIDNGVVNGDTGYILRFGALMLGVSLIQLVCNVGAVYYGARTAAAVGRDVRAAVFDRVQSFSARELGQFGAPSLITRTTNDVQQVQMLVLMTFTLMVSAPIMCVGGIAMALSLDVQLSGVLLAVVPVLGISVGAVVFRTRPLFRQMQERLDTVNRVLREQITGNRVIRAFVRDDYEKDRFREANADLTGVSLAAGKLLALMFPTVIVVVNISSVAVIWFGAMRVDSGGMEIGQLTAFLAYLMQIVMSVMMATFMFMMVPRAEVCAERIQEVLDTESSVVPPADPVRELARSGLLELRGADFRYPGAEAPVLRGVDLVARPGETTAVIGSTGSGKSTLLGLVPRLFDATGGEVLVDGEDVRRLDPELLAKTVGMVPQKPYLFSGTIASNLRYGRPDASDEELWQALEVAQAKEFVSALEGGLQAPVTQGGTNVSGGQRQRLAIARTLVQRPEIYLFDDSFSALDYATDAALRAALARETEDATVVIVAQRVATIRDADRIIVLDEGQVVGEGRHHELMAGNETYREIVLSQLTEAEAA
>NZ_CP019798.1|WP_076043593.1|2796130_2798053_+|ABC-transporter-ATP-binding-protein
MSGPGGRMMMGPAQRSLDFKGSGRRLLAQIAQDRAKLWGMVLAVVGSVACAVVGPKILGEATDLVFAGIVGREMPAGVTKQQALDGMRARGEDGMADMLSGTDFTPGRGIDFGAVGAVAIWALVVFTLAGLLMLVATRLSNHVMNGTLYRMREELQAKLSRLPLAYFDQQKRGEVLSRATNDIDNIGQTLQQTMGQLLNSLLTIVGVLAMMFWISPLLALVAVGTVPVSVYVAAKIGKKSQPQFVEQWKTTGALNAHIEEMYSGHNLVKVFGRQKESAALFAEQNEALYRASFKAQLVSGIMQPVMFFISNINYVLIAVVGGLRVASGTLSIGDVQAFIQYSRQFSMPLTQVASMANLVQSGVASAERVYELLDAPEQERDADVPERPQELRGQVTFDKVAFRYEPDRPLIENLSLSVDPGHTVAIVGPTGAGKTTLVNLLMRFYEVTGGEIALDGVDIAKMTREELRGGIGMVLQDTWLFGGTIAENIAYGASRPVTRAEIEEAARAAHADRFIRTLPDGYDTVLDDEGSGVSAGEKQLITIARAFLSDPVILVLDEATSSVDTRTEVLIQKAMARLAHGRTSFVIAHRLSTIRDADLILVMESGSIVEQGTHEELLASGGAYARLYAAQFAQAVAEVD
>NZ_CP019798.1|WP_078094202.1|2799422_2799866_+|hypothetical-protein
MTFDFEAEWTRAKGDAALRLASAGPSPSPTPSASPSATPAPAAGDPDLALVHGPVRSKASGIRTANAEARGKSTLDDAEAVGRSHAGWAAGTASNDCVAAWQRRLRELADLVDDAADALTAGTNAVNAEDQAIADRLRAAGGVLEDA
>NZ_CP019798.1|WP_078094203.1|2799865_2801227_+|hypothetical-protein
MVSVSELKQADPQKWRTAADDAVAVAKQCDGLASYARQDVARTVDRCWVGEAGRAATERFVKHADDYETSALALRAMAKVYDDLAEAITGAQRDLNSALDYARARELKVDDSGRVQLSKPVMVPQGSTEHLEPVNHAQGIITEALRKAGQADVDTARALRTIEGLTAVSDPKLAKEALTPGSPLAVALALAGGTDGLHPINVSPAQFAAVNRAAAETGISRKLLLAILWQEQQWYQNFSPGLTGPLAQAGRIFNWTLQQTLKPDKSLGITHMKPDTARAVMGDNRRAFTLPDGTFLGDLDDAQLTKYIEENPDENIRMSAYHLQRMQEEPYGARTDKQLFTLYAADTPEVRELNEQYGDESGNRAFDIKTRGENWDRLEPHLDDAMAWHALTEEQRATAVRQLESQTPAGHHVSVDPIYHEGGGPHTGTGTGPAEPGTPSPSPGPAPTPPRSN
>NZ_CP019798.1|WP_076043612.1|2801332_2801695_+|hypothetical-protein
MPSNVPTGPEYASVDDVVTALGKGGFDCKVTLRNENKFGSDAVCEVQHRGTTVYNHVSVLSTARYSRDEIGDSIEAGRRAYGHTIVAAGNWFIWVRPGVYAYDMAAALPGSVVLEPLPAK
>NZ_CP019798.1|WP_078094204.1|2801746_2803840_-|molybdopterin-oxidoreductase-family-protein
MHTPGATAATATHCPYCALQCGMNLRPGPGGAGVTVEERADFPVNRGALCGKGRTAPAVLSSRVRLTEPLVRTHAGRLEPATWEEALDTVAAGLARTARAHGPDAVGVFGGGGLTNEKAYALGKFARVALRTSQIDYNGRFCMSSAAAAHQKAFGLDRGLPFPLEDIPRTGCVILVGSNLAETMPPALRFLTELKANGGTLIVIDPRRTRTAEQADLHLAPRPGTDLALALGLLHLVVADGRTDEEFIAARTTGWEEARAAAMAHWPELVERITGVPVPALRAAVGLFCAPESAMVLTARGPEQQSKGTDTVGAWINLCLATGRAGRPLSGYGCLTGQGNGQGGREHGQKADQLPGYRKLTDPAARAHVAGVWGVDPDSLPGPGRSAYELLDALGGDVKSLLLMGSNPVVSAPRAAHIEDRIRSLDFLAVADVVLSETAALADVVLPVTQWAEETGTTTNLEGRVLLRRRALTPPPGVRSDLDVLHGLAARLGVEKGFPTAPEEVFDELRRASAGGPADYSGITYDRIEAEQGVFWPCPEGSAGTERLFLDRFATDDGRARFVPVAHRDAAEVPDADYPLLLTTGRVVAQYQSGAQTRRVDELNEAAPGPFVELHPRLAARLGAVDGSPLVVTSRRGRAVAPARITDAIRADTVFMPFHWPGEGRANTLTNPALDPTSRMPEFKVCAVRVEPAQGPV
>NZ_CP019798.1|WP_159050726.1|2803886_2804048_-|hypothetical-protein
MVCLLPERGLLNLYVVGRRIVYVEIIDRPPMRRGTAAASPVGPGGAEVPVREV
>NZ_CP019798.1|WP_030841052.1|2804106_2804877_-|glucose-1-dehydrogenase
MAVVDLSGKAVVITGAARGLGAAAAQAVVDGGGRVLITDVLAAEGAETAARLGGAARFIRHDVTSEDDWAAALEYAVAEFGRIDGLVNNAGIASGRLLEHESVESFRRVVEINLVGVFIGIKTAIPLLRANGGGSVVNISSAAGLTGLALTAGYGASKWGVRGLSKIGAVELAEAGIRVNSVHPGMTLTPMTAPVGIQAGEGNYPGAPMGRVGVPEEVAAAVAFLLSDAAAYMTGAELAVDGGWTAGLTVKHLTGR

Crispr_ID: NZ_CP019798_8

• CRISPR_ID: NZ_CP019798_8
• CRISPR_location: 4720710-4720811
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_8

Consensus_repeat	Method
AATCGCTACGCGCTCCTGTCGAGAGGCGTCTGCCAGCC	CRISPRCasFinder

spacers of NZ_CP019798_8

>8.1|4720748|26|NZ_CP019798|CRISPRCasFinder
TCTTGGGCCGGACATAGGCCGCCACC

CRISPR arrays and Neighbor proteins around NZ_CP019798_8

CRISPR arrays

The CRISPR arrays of NZ_CP019798_8

>merge|NZ_CP019798|8|4720710-4720811|CRISPRCasFinder
AATCGCTACGCGCTCCTGTCGAGAGGCGTCTGCCAGCCTCTTGGGCCGGACATAGGCCGCCACCAATCGCTACGCGCTCCTGTCGAGAGGCGTCTGCGAGCC

>NZ_CP019798|8|5|4720710-4720811|CRISPRCasFinder
AATCGCTACGCGCTCCTGTCGAGAGGCGTCTGCCAGCC	TCTTGGGCCGGACATAGGCCGCCACC
AATCGCTACGCGCTCCTGTCGAGAGGCGTCTGCGAGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_159425566.1|4713640_4714387_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|182059
NZ_CP019798.1|WP_078094884.1|4715835_4717722_+|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|341233
NZ_CP019798.1|WP_030012116.1|4725421_4725625_-|cold-shock-protein	unknown	unknown	gnl|CDD|224197
NZ_CP019798.1|WP_173675345.1|4718512_4719880_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP019798.1|WP_078094890.1|4726933_4728715_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP019798.1|WP_078094887.1|4722555_4723152_-|dihydrofolate-reductase-family-protein	unknown	unknown	gnl|CDD|334719
NZ_CP019798.1|WP_143568831.1|4721994_4722489_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094886.1|4719944_4720145_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078096291.1|4712900_4713314_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_CP019798.1|WP_078094883.1|4715011_4715638_-|hypothetical-protein	unknown	unknown	gnl|CDD|237537
NZ_CP019798.1|WP_078094880.1|4711896_4712754_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379262
NZ_CP019798.1|WP_159425567.1|4730621_4731101_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_CP019798.1|WP_078094882.1|4714576_4714960_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094879.1|4711708_4711900_-|DUF397-domain-containing-protein	unknown	unknown	gnl|CDD|377231
NZ_CP019798.1|WP_159425642.1|4723617_4725207_+|hypothetical-protein	unknown	unknown	gnl|CDD|381602
NZ_CP019798.1|WP_060179513.1|4728792_4729992_+|dehypoxanthine-futalosine-cyclase	unknown	unknown	gnl|CDD|274731
NZ_CP019798.1|WP_078094889.1|4725862_4726726_+|menaquinone-biosynthesis-protein	unknown	unknown	gnl|CDD|270352
NZ_CP019798.1|WP_060179516.1|4731155_4732061_-|DUF3152-domain-containing-protein	unknown	unknown	gnl|CDD|371483
NZ_CP019798.1|WP_076043890.1|4730011_4730656_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_076043881.1|4717810_4718296_+|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224759

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_159425566.1|4713640_4714387_+|helix-turn-helix-domain-containing-protein	gnl|CDD|182059	PRK09752, PRK09752, AIDA-I family autotransporter YfaL.	2.31885e-06
NZ_CP019798.1|WP_078094884.1|4715835_4717722_+|long-chain-fatty-acid--CoA-ligase	gnl|CDD|341233	cd05907, VL_LC_FACS_like, Long-chain fatty acid CoA synthetases and Bubblegum-like very long-chain fatty acid CoA synthetases. This family includes long-chain fatty acid (C12-C20) CoA synthetases and Bubblegum-like very long-chain (>C20) fatty acid CoA synthetases. FACS catalyzes the formation of fatty acyl-CoA in a two-step reaction: the formation of a fatty acyl-AMP molecule as an intermediate, and the formation of a fatty acyl-CoA. Eukaryotes generally have multiple isoforms of LC-FACS genes with multiple splice variants. For example, nine genes are found in Arabidopsis and six genes are expressed in mammalian cells. Drosophila melanogaster mutant bubblegum (BGM) have elevated levels of very-long-chain fatty acids (VLCFA) caused by a defective gene later named bubblegum. The human homolog (hsBG) of bubblegum has been characterized as a very long chain fatty acid CoA synthetase that functions specifically in the brain; hsBG may play a central role in brain VLCFA metabolism and myelinogenesis. Free fatty acids must be "activated" to their CoA thioesters before participating in most catabolic and anabolic reactions.	0
NZ_CP019798.1|WP_173675345.1|4718512_4719880_+|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].	5.00541e-60
NZ_CP019798.1|WP_078094890.1|4726933_4728715_+|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.	6.91032e-89
NZ_CP019798.1|WP_030012116.1|4725421_4725625_-|cold-shock-protein	gnl|CDD|224197	COG1278, CspC, Cold shock proteins [Transcription].	2.48463e-36
NZ_CP019798.1|WP_078096291.1|4712900_4713314_+|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.85716e-10
NZ_CP019798.1|WP_078094883.1|4715011_4715638_-|hypothetical-protein	gnl|CDD|237537	PRK13875, PRK13875, conjugal transfer protein TrbL; Provisional.	0.00588465
NZ_CP019798.1|WP_078094880.1|4711896_4712754_-|helix-turn-helix-domain-containing-protein	gnl|CDD|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	5.51792e-08
NZ_CP019798.1|WP_159425567.1|4730621_4731101_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	3.40058e-15
NZ_CP019798.1|WP_078094887.1|4722555_4723152_-|dihydrofolate-reductase-family-protein	gnl|CDD|334719	pfam01872, RibD_C, RibD C-terminal domain. The function of this domain is not known, but it is thought to be involved in riboflavin biosynthesis. This domain is found in the C-terminus of RibD/RibG, in combination with pfam00383, as well as in isolation in some archaebacterial proteins. This family appears to be related to pfam00186.	4.63266e-23
NZ_CP019798.1|WP_078094879.1|4711708_4711900_-|DUF397-domain-containing-protein	gnl|CDD|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	5.16947e-18
NZ_CP019798.1|WP_159425642.1|4723617_4725207_+|hypothetical-protein	gnl|CDD|381602	cd13399, Slt35-like, Slt35-like lytic transglycosylase. Lytic transglycosylase similar to Escherichia coli lytic transglycosylase Slt35 and Pseudomonas aeruginosa Sltb1. Lytic transglycosylase (LT) catalyzes the cleavage of the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc) as do "goose-type" lysozymes. However, in addition to this, they also make a new glycosidic bond with the C6 hydroxyl group of the same muramic acid residue. Proteins similar to this this family include the soluble and insoluble membrane-bound LTs in bacteria, the LTs in bacteriophage lambda, as well as the eukaryotic "goose-type" lysozymes (goose egg-white lysozyme; GEWL).	1.01676e-21
NZ_CP019798.1|WP_060179513.1|4728792_4729992_+|dehypoxanthine-futalosine-cyclase	gnl|CDD|274731	TIGR03699, menaquin_MqnC, dehypoxanthine futalosine cyclase. members of this protein family are involved in menaquinone biosynthesis by an alternate pathway via futalosine. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP019798.1|WP_078094889.1|4725862_4726726_+|menaquinone-biosynthesis-protein	gnl|CDD|270352	cd13634, PBP2_Sco4506, The conserved hypothetical protein SCO4506 exhibits the type 2 periplasmic-binidng protein fold. This group includes the SCO4506 protein from Streptomyces coelicolor and related hypothetical proteins. SCO4506 is an ortholog of Ttha1568 (MqnD) from Thermus thermophilies HB8. MqnD is an enzyme within an alternative menaquinone biosynthetic pathway that catalyzes the conversion of cyclic de-hypoxanthine futalosine to 1,4-dihydroxy-6-naphthoate. Menaquinone (MK; vitamin K) is an essential lipid-soluble carrier that shuttles electrons between membrane-bound protein complexes in the electron transport chain. SCO4506 has significant structural homology with the members of type 2 periplasmic-binding fold protein superfamily. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.33908e-109
NZ_CP019798.1|WP_060179516.1|4731155_4732061_-|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.	2.98399e-36
NZ_CP019798.1|WP_076043881.1|4717810_4718296_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	2.65336e-15

Protein sequences

>NZ_CP019798.1|WP_078094886.1|4719944_4720145_-|hypothetical-protein
MTSIHRLALLKAAIAVGALRVAPGVITGLSMERAATGALIPMRPDSRGGPQRPQRASLRSHWSDAA
>NZ_CP019798.1|WP_173675345.1|4718512_4719880_+|MFS-transporter
MLMTVLDGSIVTVAMPAIQSDLGFTPAGLSWVVNAYLIAFGSLLLLAGRLGDLLGRKRMFLAGTGLFTAASLLAGAAATPAVLIAARFLQGVGSAMASAVSLGILVTLFTEPRERARAIAVFSFTGAAGASIGQVLGGVLADALTWNWIFLINLPIGIAALLVALPTLPEDRGLGLKAGADTFGALLVTSGLMLGIYTVVKIDQYGAASAHTLGLGGLSLALLAGFLVRQATARNPLMPLRIFRSPSVTGANLVQMLMVAALFSFQILVALYMQNVLGYGAAETGLGMLPAAAAIGVVSLTVSARLNARFGERRVLLAGLVLLIGVLGLLTRVPADAEQSHYVTDLLPVMLLAAGFGLALPALTSLGMSGAKEEDAGLASGLFNTTQQIGMALGIAVLSTLAASRTESLTAAGRPASEALTGGYHLAFAVGAALLATALAVAATILRRRPSTPAP
>NZ_CP019798.1|WP_076043881.1|4717810_4718296_+|winged-helix-turn-helix-transcriptional-regulator
MTAMAPTRTEPDLSFLLDHTSHVLRTRMSAQLAEIGLTPRMHCVLVHALEEERTQAQLAEIGDMDKTTMVVTVDALEKAGLAERRPSSTDRRARIIAVTEAGAKVAKQSQKIVDGVHAGALDSLPADEREVLLRALNRLVTGHLETPVEGPRPARRARQKG
>NZ_CP019798.1|WP_078094884.1|4715835_4717722_+|long-chain-fatty-acid--CoA-ligase
MSRGGCAVEAEPKPVEPVRTVVDGVVREVRVPALAAAPAHGSLGDIPFDNAAQAPNEAVLARKQADGTWRDVTAAEFAAEVLAVAKGLIAEGLREGDRLAIMARTTYEWTLLDFAGWAAGLVTVPIYPTSSALQARWIIHDSGAVACAVEDTAQARIISAERINLPGLAHLWEFDTGAIGRLVKAGERIPDALVHARRGNRTPDSVATLIYTSGTTGRPKGCVITHANFFAEVDNSIELLHPVFKSVSKEPASTLLFLPLSHVFGRMVAVGCLRARVKLGHAPSIRTEDLLADLAGFRPTFLLAIPYVLEKVYNTARATAEKMGRASSFDRAARIARRFGESTEGKAPGPVLRAARALYDPLVYRRIRTALGGRVRYILSGGSPLGRRLAAFYTGAGIEVFEGYGLTETTGASTVTPPQRPRLGTVGWPLPGTAVRIAPDGEVLLGGRHVFAGYWNSGQALPYGSWLATGDIGELDADGYLTITGRKKDLIITSGGKNVAPAPLEDWLRAHPLVGQCMVVGDNRPYIAALITLEPDGLWHWRQMRKKQNVPMRELVRDEELLADLQRAVDEANQLVSRAESIRRFAVLPGDFTEERGHLTPSLKLRRDAIARDYADRIDELYRGPRQA
>NZ_CP019798.1|WP_078094883.1|4715011_4715638_-|hypothetical-protein
MHTTMTGLGWARAAGAVVGAMLVAGCGGGSAVPPGGALPATPSAPAPAPTAFGKEAVRADLAAATAAAGLPGKTTSLSATPPASPYPAGSPATDRERARDEVVARMATCSVGWSSPTDPGSAQDRAEARKRFHAALAGLVERGWKESRPVEEVPVGKGSMVMAQYKKQDWTLHARHVESGLLDTATMTATEDACGARFTDAELNLLED
>NZ_CP019798.1|WP_078094882.1|4714576_4714960_-|hypothetical-protein
MHEESLPTPEPGTWYPVDGLGDTIGERWLRLRQRLGVRDRSNLRELVEAAFAEPRLRALSPGTSVYWLRFSRRAAPPIFGDLPLARALRDGRYEVRTPDGRLQEAASTAAAVSLLVAALPPDIPTSA
>NZ_CP019798.1|WP_159425566.1|4713640_4714387_+|helix-turn-helix-domain-containing-protein
MVGNHLLQHRELSATAIGVAAYIQSLPDGAPVGIKALVARFPEGEVRIASALRELERHGYLERRRERLEGGRVVTRTYSYNKPGSASGEPPPPPDREPVPEPESDPEPDPAPEREAAVAPEAQRLHPGAADLLAGLRRRDPRLLLAERDVRRLAPCVSAWLERGVDPEAVARALSSGLPEDMRRPASVLAYRLTALLPPHLPAAPPQPAARPPARPDPLQNCDGCDKAFRAPTPGRCRSCPPAAAAAA
>NZ_CP019798.1|WP_078096291.1|4712900_4713314_+|ATP-binding-protein
MSDVIPQLVDFHVQLSATPRAARLARLLTVEQLRGWGLPLVEPAHIVAELAANAVTHGRVPGRDFRLALKATPEVLLIEVTDARGDRVPRIRDAGCGLVIVEALAERWGVREGPPPCKVVWAEVLTTGSRRPATRRA
>NZ_CP019798.1|WP_078094880.1|4711896_4712754_-|helix-turn-helix-domain-containing-protein
MSVDSDGTEEPGWDVDPEDEQGAAVVAALGRQLKAWREAAGLRPADFGAAIRYGEDQVRKVESGKRIPRPEYLDRADEVLDAGGRISAMKADLEQVRYPKKVRDLAKLEARAVEIGSYGNHNIHGLLQTEEYARALFEMAQPPQSPEEVERGVAARLARQAIFDRSPGPALSFVQEEVTLRRTIGGTMVRRAQLERLLELGQLRNVTIQVMPTNCADHAGMEGLIQVLKFADGSAVGRGEGIFNGRPVSDPKQLRILDLQYGMIRAQALSPRESRAFVEKLLGET
>NZ_CP019798.1|WP_078094879.1|4711708_4711900_-|DUF397-domain-containing-protein
MIHKPELEWFKSSYSDSSNINDCVEVANTPGAVLVRDSKDTARAHLAFGRPAWEGFVAQASEV
>NZ_CP019798.1|WP_143568831.1|4721994_4722489_+|hypothetical-protein
MTLAVAGWLMWVLPGPQLGAVLGLGPVDGVVSVHRCYEATDAEGYATGTDCTGWYTPRRAGEEAREIVLDTAADEYRRGTQVEVRTARGRAYELSGTAVFNFGSAAGLLLVPFLTLAAWLFACARSGAVESGDGYFLVSLAGLLAAIVLAAVAGILVGIATAVF
>NZ_CP019798.1|WP_078094887.1|4722555_4723152_-|dihydrofolate-reductase-family-protein
MRIVITEFISLDGVVQAPGGPGEDGDGGFAHGGWTQPFFDPEVVGGSFTEALEKADALLYGRRTWQNMAAAWPERAGDPFADRMNAIPKYVVSDTLGDDELTWNNTTRIDGGKAVARIRELRDGDGGDLVVMGSPTLARTLLSEGLVDELRLMIMPVLLGGGKSIFPQDGGLHTLELTSTAISPAGVHVCTYRPTAKA
>NZ_CP019798.1|WP_159425642.1|4723617_4725207_+|hypothetical-protein
MTTAAVVSTPSTADAGESEPTPDSPQATDRGDARLDLPDIVADPPPAAGTGTQEAGASGIPATALDAYNRAEVAVAAALPNCKLPWQLLAGIGRVESVHASGYGLKADGYTEKPIRGPRLDGNGFAEIRDTDRGEFDADVVYDRAVGPMQFIPSTWATWGADGNGDAKRDPNNIYDAALGAGLYLCAGDRNLSVAAELDKAILSYNNSREYVNTVLGYMHQYQQGATEVANPPVGNYPPAQPGTLPTPRPQTPVTPTPAPKPTPTPTPKPTPTPTPTPTPTPTPEKPAPHLADLTVLDGPGLAAEAGTAFTVVPRVKLLLSDGKPAAGREVIFAVEEDATGTLFGTAKSLVVKTGADGIAAAPGLKAGATAGTFTLRASAYDTTSRLTVNFAGKVTAPAADLLARPDGSKPIVAAAGTSITGVEVRATAKGKAVAVSGVVAGLGQEKDGKWVPADPATAKGPYFKDATGKKAFSLTLAATAADGRIVLPELFTDADLAPGTYQLRLVTPEDVTLILDIEITAPPAATAK
>NZ_CP019798.1|WP_030012116.1|4725421_4725625_-|cold-shock-protein
MATGTVKWFNAEKGFGFIAQDGGGPDVFVHYSAINASGFRSLEENQTVNFDVTQGPKGPQAENVTPA
>NZ_CP019798.1|WP_078094889.1|4725862_4726726_+|menaquinone-biosynthesis-protein
MDVYRSRPRVGHIQFLNCLPLYWGLARTGTLLDLELTKDTPEKLSQRLVDGELDIAPITLVEFLRNADRLVAFPDLAVGCDGPVMSCVIVSQVPLDRLDGARVALGSTSRTSVRLAQLLLSEQYGVRPDYYTCPPDLGVMMQEADAAVLIGDAALRASLHDAPRLGLTVHDLGHMWKEWTGLPFVFAVWAARKDYLTREPAVVQKVHEAFLASRDLSLEEVAKVAEQAARWEAFDAELLERYFTTLDFRFGPDQLAGVREFARRTGPTTGYPADVSVELLGAVVREC
>NZ_CP019798.1|WP_078094890.1|4726933_4728715_+|serine/threonine-protein-kinase
MHPLEAGEPRTIGAYRLLGRLGAGGMGRVYLGRSAGGRTVAVKIVHPHFASDEEFRARFRREVEAARRVGGEWTAPVLDADPEAPVPWVATGYVAGPSLARALAAHGPLPEPSVRAVGAGLARALVAVHGLGLVHRDVKPSNVMLALDGPRLIDFGIARAMDGTASLTSTGVSVGSPGYMSPEQILGKGITGAADVFSLGAVLAFAATGRPPFTGDNSATLLYKVVHEPPELGDLPAGDLRDLIEACLAKAAADRPAPEAVAAALAGALGAPGWLPAPLVEEASRAAVALLDLDADSPEGAAAGGPAPAGAGAGAAPEAASGPVPFAAGSYAPAGGGFGAPDPSYGSRGAGFPYAAPAAGPYASPTETAGAGPAGAAGAAAGAVPQPRSEPGGPQVSLRAAGRRFSCTVVLAAAAVLAVLSGGVYFLDLLPGQGGDRQRDLADAGARPSASSPAPGASAPAPVASSASPAPGTRTDVPKELIGTWKGTVTTARLGLSSEFEITIKGGKVGEVVARDKSVLAVLGTDCSGDWKLSSATDRSLVLDTSAGPNPAPGVCSNGSADERFTLNADGTLHYKSGDTPAGNPEGDLRRSP
>NZ_CP019798.1|WP_060179513.1|4728792_4729992_+|dehypoxanthine-futalosine-cyclase
MTDQAVLQSVLDRAAAGGRITKEEALDLYRHAPLHALGQAADAVRRRRYAGTEHIATYIIERNINYTNVCVTACKFCAFYAAPKDTKKGWSRDLDDILRRCAETVELGGTQIMFQGGHHPDYGVEYYEHHFAAIKQAFPQLVIHSLGASEVEHMARISGVSAEEAIKRIHAAGLDSFAGAGAELLPARPRKAIAPLKESGERWLEIMEIAHKLGVESTSTMLMGTGETNAERIEHIAMIRDTQDRTGGFRAFIPYTYQPENNHLKGRTQATIFEYLRMIAVARLFLDNIAHIQGSWLTVGKEAGQLSLHYGADDLGSIMLEENVVSSAGAKHRSNRQEIIDLIRKAGRTPAQRATTYEHLLVHDDPANDPADDRVVSHISSTAIEGGTAHPELKLISAN
>NZ_CP019798.1|WP_076043890.1|4730011_4730656_+|hypothetical-protein
MLTLHAAELLVTGPGSAPLAGGAVLVEGDRIARVGTYEDLGSAHSHARVRRWPGVLTPGLLVRGADELLERTYYPDDPYEVTELGADPITGGEALEALKLTESRWGNSARRGTQRLLARGVVAVCGRFTVAAVRTAVSRSGLAILPPAPYEGRPDLDPFAGRESAAEAFHGVLEPGAAARFAVFAVADEAELLTRGATACVATVIGGRLLHRRR
>NZ_CP019798.1|WP_159425567.1|4730621_4731101_-|helix-turn-helix-transcriptional-regulator
MRVVSFSVPAWFPSYEEPDGPPAQDEAQPWEALLTEQESAVFLCLATGASNRELAGELQLSVSTVKFHVVNIRAKLGGISRLQACLLAALAREGSRPADAGPGEDALDGGRPGENEPAGSAAAGSRPGENAPGENAPAESEPGGSDGGLSAAGAAAVPR
>NZ_CP019798.1|WP_060179516.1|4731155_4732061_-|DUF3152-domain-containing-protein
MPAGHSTGRSRRDGPRARRRAERRRRLRRTILLGSAALVAVSATAYALLPEDETTTAAKGRTAAQADAPDGEGTDAAGNPLPQGGAKSPEAAPSPAAPSPQAPSPSPSTGAPATPGKPGTFTGSSASGSAQGKGTTRRWRLEVEEGSGIDPEAAARSVEAILGDPRGWTRDPRYGFQLVGAGQPVDFTVKIATPKTTDLLCDVVTPELIGETNCRVGHVVVVNLKRWKEGSPQFSGSVEEYRALIVNHEVGHEIGRGHEGCPGPGKPAPAMMQQIKGLGGCKSNAWPFDANGTYLSGPPVL

Crispr_ID: NZ_CP019798_9

• CRISPR_ID: NZ_CP019798_9
• CRISPR_location: 4885757-4886054
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 6 spacers

Consensus repeat of NZ_CP019798_9

Consensus_repeat	Method
TGCGGGCGGCTCGGCGGT	CRT

spacers of NZ_CP019798_9

>9.1|4885775|36|NZ_CP019798|CRT
CACATATCGCCCGAACCGGGCCCCTACGGGGTGCCC
>9.2|4885829|28|NZ_CP019798|CRT
GTACGGCTCGCTCCTGGCGGGGGTGTCG
>9.3|4885875|25|NZ_CP019798|CRT
ACCCTCCGGCTCGGCGCCGGGCCCG
>9.4|4885918|27|NZ_CP019798|CRT
GTGCGGCTGGATCCGGGCGGGGTGTCG
>9.5|4885963|28|NZ_CP019798|CRT
CCCCTGGGCGGGGTTACTGCGGGTGCCC
>9.6|4886009|28|NZ_CP019798|CRT
GTGCGGCCGGATCCCGGCAGGGGTGTCG

CRISPR arrays and Neighbor proteins around NZ_CP019798_9

CRISPR arrays

The CRISPR arrays of NZ_CP019798_9

>merge|NZ_CP019798|9|4885757-4886054|CRT
TGCGCACGGCTCAAGCGTCACATATCGCCCGAACCGGGCCCCTACGGGGTGCCCTGCGGGCGGCTCGGCGGTGTACGGCTCGCTCCTGGCGGGGGTGTCGTGCGGGCGGCTCGGCGGTACCCTCCGGCTCGGCGCCGGGCCCGTGCGTGGTGCTCGGCGGTGTGCGGCTGGATCCGGGCGGGGTGTCGTGCGGGCGGCTCGGCGGGCCCCTGGGCGGGGTTACTGCGGGTGCCCGGCGGGCGGCTCGGCGGTGTGCGGCCGGATCCCGGCAGGGGTGTCGTGCGGGCGGTTCGGCGGT

>NZ_CP019798|9|4|4885757-4886054|CRT
TGCGCACGGCTCAAGCGT	CACATATCGCCCGAACCGGGCCCCTACGGGGTGCCC
TGCGGGCGGCTCGGCGGT	GTACGGCTCGCTCCTGGCGGGGGTGTCG
TGCGGGCGGCTCGGCGGT	ACCCTCCGGCTCGGCGCCGGGCCCG
TGCGTGGTGCTCGGCGGT	GTGCGGCTGGATCCGGGCGGGGTGTCG
TGCGGGCGGCTCGGCGGG	CCCCTGGGCGGGGTTACTGCGGGTGCCC
GGCGGGCGGCTCGGCGGT	GTGCGGCCGGATCCCGGCAGGGGTGTCG
TGCGGGCGGTTCGGCGGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_159425568.1|4878255_4878417_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078094922.1|4878035_4878263_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030851491.1|4888216_4889845_+|chaperonin-GroEL	unknown	unknown	gnl|CDD|234573
NZ_CP019798.1|WP_030851478.1|4892305_4893205_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176115
NZ_CP019798.1|WP_030856214.1|4876826_4877036_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_076046775.1|4889909_4890620_-|ester-cyclase	unknown	unknown	gnl|CDD|377824
NZ_CP019798.1|WP_078094920.1|4874442_4875312_+|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl|CDD|213022
NZ_CP019798.1|WP_060178865.1|4890725_4891499_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|223377
NZ_CP019798.1|WP_078094929.1|4895116_4895746_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|236607
NZ_CP019798.1|WP_078094924.1|4879814_4880480_-|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223943
NZ_CP019798.1|WP_030011064.1|4887795_4888104_+|co-chaperone-GroES	unknown	unknown	gnl|CDD|178988
NZ_CP019798.1|WP_078094928.1|4891530_4892217_-|MOSC-domain-containing-protein	unknown	unknown	gnl|CDD|225167
NZ_CP019798.1|WP_078094926.1|4882378_4883614_-|LCP-family-protein	unknown	unknown	gnl|CDD|224235
NZ_CP019798.1|WP_030027725.1|4893412_4893739_-|WhiB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376791
NZ_CP019798.1|WP_060178871.1|4880996_4882391_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	unknown	unknown	gnl|CDD|223843
NZ_CP019798.1|WP_030855996.1|4877249_4878008_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_CP019798.1|WP_107499907.1|4883671_4885084_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP019798.1|WP_159425569.1|4887053_4887536_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_003948568.1|4894129_4894741_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP019798.1|WP_078094923.1|4878607_4879834_+|transcriptional-regulator	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_030851491.1|4888216_4889845_+|chaperonin-GroEL	gnl|CDD|234573	PRK00013, groEL, chaperonin GroEL; Reviewed.	0
NZ_CP019798.1|WP_030851478.1|4892305_4893205_+|LysR-family-transcriptional-regulator	gnl|CDD|176115	cd08423, PBP2_LTTR_like_6, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator, contains the type 2 periplasmic binding fold. LysR-transcriptional regulators comprise the largest family of prokaryotic transcription factor. Homologs of some of LTTRs with similar domain organizations are also found in the archaea and eukaryotic organisms. The LTTRs are composed of two functional domains joined by a linker helix involved in oligomerization: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal substrate-binding domain, which is structurally homologous to the type 2 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcriptional repressor undergoes a conformational change upon substrate binding which in turn changes the DNA binding affinity of the repressor. The genes controlled by the LTTRs have diverse functional roles including amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to a name a few. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.00869e-56
NZ_CP019798.1|WP_076046775.1|4889909_4890620_-|ester-cyclase	gnl|CDD|377824	pfam07366, SnoaL, SnoaL-like polyketide cyclase. This family includes SnoaL a polyketide cyclase involved in nogalamycin biosynthesis. This family was formerly known as DUF1486. The proteins in this family adopt a distorted alpha-beta barrel fold. Structural data together with site-directed mutagenesis experiments have shown that SnoaL has a different mechanism to that of the classical aldolase for catalyzing intramolecular aldol condensation.	3.16972e-28
NZ_CP019798.1|WP_078094920.1|4874442_4875312_+|polysaccharide-deacetylase-family-protein	gnl|CDD|213022	cd10917, CE4_NodB_like_6s_7s, Catalytic NodB homology domain of rhizobial NodB-like proteins. This family belongs to the large and functionally diverse carbohydrate esterase 4 (CE4) superfamily, whose members show strong sequence similarity with some variability due to their distinct carbohydrate substrates. It includes many rhizobial NodB chitooligosaccharide N-deacetylase (EC 3.5.1.-)-like proteins, mainly from bacteria and eukaryotes, such as chitin deacetylases (EC 3.5.1.41), bacterial peptidoglycan N-acetylglucosamine deacetylases (EC 3.5.1.-), and acetylxylan esterases (EC 3.1.1.72), which catalyze the N- or O-deacetylation of substrates such as acetylated chitin, peptidoglycan, and acetylated xylan. All members of this family contain a catalytic NodB homology domain with the same overall topology and a deformed (beta/alpha)8 barrel fold with 6- or 7 strands. Their catalytic activity is dependent on the presence of a divalent cation, preferably cobalt or zinc, and they employ a conserved His-His-Asp zinc-binding triad closely associated with the conserved catalytic base (aspartic acid) and acid (histidine) to carry out acid/base catalysis. Several family members show diversity both in metal ion specificities and in the residues that coordinate the metal.	2.48405e-31
NZ_CP019798.1|WP_030011064.1|4887795_4888104_+|co-chaperone-GroES	gnl|CDD|178988	PRK00364, groES, co-chaperonin GroES; Reviewed.	3.70061e-48
NZ_CP019798.1|WP_060178865.1|4890725_4891499_-|SDR-family-oxidoreductase	gnl|CDD|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	2.8871e-79
NZ_CP019798.1|WP_078094924.1|4879814_4880480_-|HAD-family-hydrolase	gnl|CDD|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	1.14703e-23
NZ_CP019798.1|WP_078094926.1|4882378_4883614_-|LCP-family-protein	gnl|CDD|224235	COG1316, LytR, Transcriptional regulator [Transcription].	2.32136e-55
NZ_CP019798.1|WP_030027725.1|4893412_4893739_-|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.	1.01236e-27
NZ_CP019798.1|WP_060178871.1|4880996_4882391_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	gnl|CDD|223843	COG0772, FtsW, Bacterial cell division membrane protein [Cell division and chromosome partitioning].	3.80269e-76
NZ_CP019798.1|WP_030855996.1|4877249_4878008_+|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	2.16592e-49
NZ_CP019798.1|WP_107499907.1|4883671_4885084_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	6.64827e-56
NZ_CP019798.1|WP_078094928.1|4891530_4892217_-|MOSC-domain-containing-protein	gnl|CDD|225167	COG2258, COG2258, Uncharacterized protein conserved in bacteria [Function unknown].	1.63845e-61
NZ_CP019798.1|WP_003948568.1|4894129_4894741_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	1.73082e-50
NZ_CP019798.1|WP_078094929.1|4895116_4895746_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|236607	PRK09648, PRK09648, RNA polymerase sigma factor ShbA.	4.68441e-88

Protein sequences

>NZ_CP019798.1|WP_107499907.1|4883671_4885084_-|HAMP-domain-containing-histidine-kinase
MAEPRRGPGGTRTARRGRPGIRARTAAAAAVAMAAVLAAGGLWLYALLRANLLDNTTGRTELAALRAAAQLDSRTPPPPGGRLPAPENGVDLVLVRDAAGRTVAATGGDPGHAPALDGAPRPGPGEDSRSAVLPPEHPGGHRRAVVAVTAPGGHTVYAVTVLGDVDDATGAVAVALLAGAPPLIAFAAALAWWVTGRALRPVDAIRTELASVTASELDRRVPDPGGADEIAQLARTVNATLDRLEHADARQRQFTADASHELRNPLAAVRSRLEVALAADRPDRESVAAALAETDRLQRIAADLLLLARLDGGPPPRAEPVDLALLAAEDAARRGGARVALRLDARAPVPAAGDPARLERALANLVDNALRHARSEVAVRAAEEDGWAVLEVTDDGPGIPDADRERVFERFVRLDADRSRAGGGTGLGLAIAREVARAHGGDVRALPTPAGGARLVLRIRRRGGDMGRQP
>NZ_CP019798.1|WP_078094926.1|4882378_4883614_-|LCP-family-protein
MSAHRRKTRTRRRPPSRRRRLGRTLLVAACALAVTAGGGAWYLYRDLAAGIGSSRALDGAEKSKFGDTNILLIGLDSRRDKNGEKLPAEVLDQLHAGSSDIGGYNANTLILLHVPGDGGRAKAFSVPRDDFVDIPGHGKDKIKKAYGLAKARKEGQLAAAGVKDARELEREGREAGRAAQIATVRGFLGVPVDHFAELNLAGFHHLAQALGGVPVCLNKAVKDTYSGADFPAGPQTLDGRQSLAFVRQRHGLDGGDLDRTKRQQAFLAGATKKLNSAGTFTDPVKLIKLIDVAKQDVVTDQGWDLLSFVKRAKSLSDGRVQFTTLPVERFGRNLGEDINVVDDMKIKRLIAEQIGPKASASPGAPSAEAGSAGSAPGARESAPPPASSPSPPASSPSPSTPEDGGGIPCVD
>NZ_CP019798.1|WP_060178871.1|4880996_4882391_-|FtsW/RodA/SpoVE-family-cell-cycle-protein
MRGLRPLTAAGARRRTEALLLVLVVAIAVFGHAAAGLAMNGELPPNLAGFTISMTLLSLVGHLGVRRFAAYADPLVFPLAMLLTGLGLVLIHRLDQGYIERWNSDANAPGQLLWTVVGVAACIAVLALLRDHRLLQRFIYITMAVALVLLIAPAFFGADTYGAKRWIILFGFSIQPGEFVKIMIAIFFAGYLVIHRDSLALTGRRFLGMRLPPMRQLGPLITVWILSMLVLVFERDLGTSLIFFGVFVVMLYVATERTGWIVCGLLMASAGAFVVGSTEPHVKARVAAWLNPLSVYWENPPPGVTSDQSAQALFSFGTGGISGTGLGMGHPELIKFAGRSDFILTTVGEELGLAGVMAVLILYALLVQRGLRMALGARDPFGKLLAVGLASALALQVFVVAGGVTGLIPLTGKALPFLAKGGSSLLANWIMIALLLRISDSAERQREADSRGPAETTLTPVVRV
>NZ_CP019798.1|WP_078094924.1|4879814_4880480_-|HAD-family-hydrolase
MTIRAVVFDVGECLVDETREYGTWADWLGVPRHTFAAMFGAVIAQGLDYREVFQPFKPGFDLTAEREARAAAGQPEHFDESDLYPDVRPALRALREAGLWLGIAGNQTVRAGGILRSLFTDDVDLIGTSDDWGASKPDPEFFVRVAKIVPFAPEEILYVGDRVDNDLRPGSAAGMRTALIRRGPWATIQWNSPEALELPTFRVESLEELPTRITDFNSSEH
>NZ_CP019798.1|WP_078094923.1|4878607_4879834_+|transcriptional-regulator
MPRPTGNARLRAARLAAGYRSQQDLIDALARRGVNVGIKQVQRWESETPPWPYPEARRALQELLGQDMEQLGFERRPGTTESGLSPARLAPPARGAVRTRNATQPASVASDYLAVTRAHRQLYWSVAPATLHPAVVAHAGLGEALLPATAGQTHQTLAAALAESHLLAGRIEFFDQRAPDRARDTWVQALQAAGEADDPLLGSAILAHMAFVPGWSGDRLAASERMIAARTYARRAPASAEFLAWLDAVEAECETRCGNTRTALNLIAHGEDVLAAGGAYASPEWMDWFSVVRLAAFKGNTELKAGRLPQARETLLRALADLPADSDKQCTVILGDLGAVEAAASNPEAAAEYALRALDLLETHWYATGLERVRDVRRALVPWQHERCVRDLDDRLYGWGSVVSALTN
>NZ_CP019798.1|WP_159425568.1|4878255_4878417_-|hypothetical-protein
MTNPTPRGVWSLDIPDSPSIGFAAVRQPSPELLARAQAGFARFTAADEVESDE
>NZ_CP019798.1|WP_078094922.1|4878035_4878263_-|hypothetical-protein
MSEQYEYVPHPLLRRRVRDIASGAEGELMAVINENVSDTGLACWMELAYIRGASGLEFTTSVANVVPAVDGQACS
>NZ_CP019798.1|WP_030855996.1|4877249_4878008_+|GntR-family-transcriptional-regulator
MTSQGATRQPKYQRIADALRKSIQAGEYGPGDRLPGENDLMAAYEVARMTARQALGVLQNEGLAEARKGAGVFVRAFRPLRRRGLQRLAQEQWGSGRSIWSTDSEDRELVVDQIDVREEEADDRVCDALGITPGTQVWARSRRFVLDGKPVLFATSYLPSDIVADSPITQRETGPGGTYARLAELGHGPVHFREEIRSRMPSADEADRLSLATGTPVIRIVRTAFAEDGRAVEVNEMTLDSASYVLEYDFDA
>NZ_CP019798.1|WP_030856214.1|4876826_4877036_-|hypothetical-protein
MSERYEHVPHRLLHRRVRDIASGVEGELVAVVNENVSNAATAHWVELAYIRGASGLEFTTSAANVEPAD
>NZ_CP019798.1|WP_078094920.1|4874442_4875312_+|polysaccharide-deacetylase-family-protein
MVAGTLAAGALALSLTGCGESVEPIERLGRKTTQEPSQTPTASATVPASSPAPAPGGASDEAYKKWGLTAPVQYAPKPAQKPQLPKAAPGKVPVIDRIPLPAGEKIVFLTFDDGAEKDPEFLKMAADLQLPISMFLTDSVASSDYGHFEKLRDNGSASTVNNHTLTHPNLRTLSFEAQKKEICGQQDKLEKRFGQRPPLFRPPFGNYNDDTLRAASECGVSSILLWRVSMQINNFQYAQGSALQPGDIILAHFRGPSELKGASEVQMTTRMLQRIQEQGYRIGRLEDYL
>NZ_CP019798.1|WP_159425569.1|4887053_4887536_-|hypothetical-protein
MTRTNSGVRWVHAVPIAIGLAVGIWMFHAAVPRLITQLTGVDGRFGAERCVWGEPDFEGERTMTCRGSFTAADGSFSLAGIRIDGVFDERPQAPVAARVSGPDADHAVQLDFLTTFAPMGLGLTAFAFPAWALTAATRDLLTRRSPAGLLGGCGGAPGRG
>NZ_CP019798.1|WP_030011064.1|4887795_4888104_+|co-chaperone-GroES
MTTASSKVAIKPLEDRIVVQPLDAEQTTASGLVIPDTAKEKPQEGVVLAVGPGRFEDGQRLPLDVTVGDIVLYSKYGGTEVKYSGEEYLVLSARDVLAIVEK
>NZ_CP019798.1|WP_030851491.1|4888216_4889845_+|chaperonin-GroEL
MAKILKFDEDARRALERGVNKLADTVKVTIGPKGRNVVIDKKFGAPTITNDGVTIAREVELDDPYENLGAQLVKEVATKTNDIAGDGTTTATVLAQALVREGLRNVAAGASPAALKKGIDAAVKAVSEDLLATARPIEDKSDIAAVAALSAQDSQVGELIAEAMDKVGKDGVITVEESNTFGLELEFTEGMAFDKGYLSPYMVSDQERMEAVLDDPYILINQGKISSIQDLLPLLEKVIQAGGSKPLLIIAEDVEGEALSTLVVNKIRGTFNAVAVKAPGFGDRRKAMLQDMATLTGATVIAEEVGLKLDQAGLDVLGSARRVTISKDDTTIVDGAGSSDEVLGRVNQIKAEIEATDSDWDREKLQERLAKLAGGVCVIKVGAATEVELKEKKHRLEDAISATRAAVEEGIVSGGGSALVHAVKVLDGNLGLSGDEATGVAVVRRAAVEPLRWIAENAGLEGYVITSKVSELDKGQGFNAATGEYGDLVKAGVIDPVKVTRSALENAASIASLLLTTETLVVEKPAEDEGDAGHGHGHGHSH
>NZ_CP019798.1|WP_076046775.1|4889909_4890620_-|ester-cyclase
MTFVQVIDYETTRFDEMNALIDRWAEQSSGRRTATHTMIGQDREARNHYVDMVEFASYEEAMKNSQLPETDRMFQEMVSLCEGMPKFMNLDVVRDEHLNKQLVNRVFQEAAMAGDMSVLDDCFATNYIDHDASKEEPTVIGRESMRSDMEMWRAAFDMTFEPTAQLAEGDMVTTVWNWRGTHKGEFMGVAPTGKTYEMSGTTTFRCLDGEIIEGWWHYNPGALQRQMGGTGTPYGT
>NZ_CP019798.1|WP_060178865.1|4890725_4891499_-|SDR-family-oxidoreductase
MTTALITGSTAGIGAAFARRLAAQGHNLVLVARDTKRLGEQATELHDLHGIEAEVLVADLSTEEGIASVEKRLGDRTHPVDLLVNNAGFGNKGRYLEVSMADELTMLKVHVEAVLRLTSAAAESMRSRGRGGVINVASVAAFVPRGTYGASKAWVVQFTQGAARDMAGSGVRLMALCPGFVRTEFHQRAGMGTDSIPGWMWLDADKLVAAALADLARGKTVSIPDPRYKALMGVVKLTPRGLLGGVSSRTGRKYGPQ
>NZ_CP019798.1|WP_078094928.1|4891530_4892217_-|MOSC-domain-containing-protein
MHLISVNVGAATPSEHTDAESGVTGIGKRPVPGPVRVFAPGDKATGLGSGLEGDAICDRRHHGGDHQAVYAYAREDLDLWERELGRDMPGGLFGENFTTSGIDLNTARLGDRWRVGADLVLEVASARIPCRTFQGALGEAGWVRRFTREARPGAYLRVIEEGSVSPGDPIEVIHRPDHDVTVQLWFRAFTTERALLPRTLAAGAAMEPEAHETVRRYVEKYGTGAGAR
>NZ_CP019798.1|WP_030851478.1|4892305_4893205_+|LysR-family-transcriptional-regulator
MIEARHLRVLRAVAGTGSFSAAARELGCTQPAVSQQMKALEQSAGTPLLIRTGREMRLTQAGEALVRHAAGILAGLTAAEEEVAAIAGLRAGRVRLVSFPSGSSTLVPTALAAMRAEHPGTRISLVEAEPPRSVEMLREGDCDLALAFRYGGAAGSAAEWEDLVVRPLLTDRLVGLVPEGHALAGAERVGMAELAGEPWIAGCPRCRRHLVEVCEEAGFTPRIDFATDDYPAVVGLVGAGLGVAVLPELAVESVRAKGVSTLVVEPAVEREVVALTLPDLARVPAVAATLAELERAAAR
>NZ_CP019798.1|WP_030027725.1|4893412_4893739_-|WhiB-family-transcriptional-regulator
MADFSRLPGPNADLWDWQLLAACRGVDSSLFFHPEGERGAARSAREASAKEVCMRCPVRSECAAHALAVREPYGVWGGLTEDEREELMGRARHRLIPASSAIGPIAPH
>NZ_CP019798.1|WP_003948568.1|4894129_4894741_+|response-regulator-transcription-factor
MTSVLVCDDSPLAREALRRAVATVPGVERVTTAANGEEVLRRWGADRSDLILMDVRMPGLGGVETVRRLLSADPGARIIMLTVAEDLDGVALAVAAGARGYLHKDASRAELRATVTQALADPTWRLAPRRLRSAEMGAAPTLTAREIQVLEGMSHGRSNAEIGRELFLSEDTVKTHARRLFKKLGASDRAHAVALGFRWGLVR
>NZ_CP019798.1|WP_078094929.1|4895116_4895746_+|sigma-70-family-RNA-polymerase-sigma-factor
MRDDEALGSPAATGTTGAAGGGSAGGVSALVRRAVEGDEQATHDLLAFVHPLAIRYCRTRLSRLPGDARHFVEDLAQEVCVAVLMALPRYRDTGRPFEAFVFAIAAHKVADLQRAAMRHPGSTAVPSDEMPERPDDSLGPEERALLSSDAAWAKKLLANLPENQRELLVLRVAVGLTAEETGQMLGMSPGAVRVAQHRALSRLRALAEQ

Crispr_ID: NZ_CP019798_10

• CRISPR_ID: NZ_CP019798_10
• CRISPR_location: 5246866-5246982
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_10

Consensus_repeat	Method
CGCTTCGGCTTGGCCGGGGCCTCCTCGGCC	CRISPRCasFinder

spacers of NZ_CP019798_10

>10.1|5246896|57|NZ_CP019798|CRISPRCasFinder
GCGACGGCGGCTTCGGCGGCGACCGGTGCGGCCTCCGCGGCCTTGCGGGTGCGAGTG

CRISPR arrays and Neighbor proteins around NZ_CP019798_10

CRISPR arrays

The CRISPR arrays of NZ_CP019798_10

>merge|NZ_CP019798|10|5246866-5246982|CRISPRCasFinder
CGCTTCGGCTTGGCCGGGGCCTCCTCGGCCGCGACGGCGGCTTCGGCGGCGACCGGTGCGGCCTCCGCGGCCTTGCGGGTGCGAGTGCGCTTCGGCTTGGCCGGAGCCTCCTCGGCC

>NZ_CP019798|10|6|5246866-5246982|CRISPRCasFinder
CGCTTCGGCTTGGCCGGGGCCTCCTCGGCC	GCGACGGCGGCTTCGGCGGCGACCGGTGCGGCCTCCGCGGCCTTGCGGGTGCGAGTG
CGCTTCGGCTTGGCCGGAGCCTCCTCGGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078095035.1|5251665_5251881_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_167389209.1|5245611_5245764_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030853473.1|5250880_5251519_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP019798.1|WP_076043388.1|5252013_5253009_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP019798.1|WP_030853443.1|5240519_5241035_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_060176943.1|5250072_5250372_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030772789.1|5250484_5250712_-|DUF3107-domain-containing-protein	unknown	unknown	gnl|CDD|378634
NZ_CP019798.1|WP_078095036.1|5253014_5254454_+|DUF3152-domain-containing-protein	unknown	unknown	gnl|CDD|371483
NZ_CP019798.1|WP_030853436.1|5238193_5239465_-|magnesium-transporter	unknown	unknown	gnl|CDD|225148
NZ_CP019798.1|WP_078095037.1|5256536_5257520_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224094
NZ_CP019798.1|WP_060176703.1|5243242_5243887_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_030853457.1|5244929_5245535_+|MarC-family-protein	unknown	unknown	gnl|CDD|225006
NZ_CP019798.1|WP_078095032.1|5241106_5242222_-|magnesium-and-cobalt-transport-protein-CorA	unknown	unknown	gnl|CDD|213364
NZ_CP019798.1|WP_060176711.1|5254800_5256540_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173871
NZ_CP019798.1|WP_078095038.1|5257516_5258509_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|223674
NZ_CP019798.1|WP_060176704.1|5243989_5244853_+|PHP-domain-containing-protein	unknown	unknown	gnl|CDD|223686
NZ_CP019798.1|WP_037834246.1|5239678_5240443_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078095034.1|5249216_5249975_+|tRNA-2-methylthio-N6-isopentenyl-adenosine(37)-hydroxylase-MiaE-like-protein	unknown	unknown	gnl|CDD|205967
NZ_CP019798.1|WP_030853448.1|5242597_5243182_+|suppressor-of-fused-domain-protein	unknown	unknown	gnl|CDD|377450
NZ_CP019798.1|WP_030853460.1|5245859_5246717_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|366166

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_030853460.1|5245859_5246717_-|alpha/beta-hydrolase	gnl|CDD|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	2.30725e-25
NZ_CP019798.1|WP_076043388.1|5252013_5253009_+|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.0629e-27
NZ_CP019798.1|WP_030853448.1|5242597_5243182_+|suppressor-of-fused-domain-protein	gnl|CDD|377450	pfam05076, SUFU, Suppressor of fused protein (SUFU). SUFU, encoding the human orthologue of Drosophila suppressor of fused, appears to have a conserved role in the repression of Hedgehog signaling. SUFU exerts its repressor role by physically interacting with GLI proteins in both the cytoplasm and the nucleus. SUFU has been found to be a tumor-suppressor gene that predisposes individuals to medulloblastoma by modulating the SHH signaling pathway. Genomic contextual analysis of bacterial SUFU versions revealed that they are immunity proteins against diverse nuclease toxins in polymorphic toxin systems.	4.79875e-27
NZ_CP019798.1|WP_030772789.1|5250484_5250712_-|DUF3107-domain-containing-protein	gnl|CDD|378634	pfam11305, DUF3107, Protein of unknown function (DUF3107). Some members in this family of proteins are annotated as ATP-binding proteins however this cannot be confirmed. Currently no function is known.	1.31035e-36
NZ_CP019798.1|WP_078095036.1|5253014_5254454_+|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.	4.83981e-56
NZ_CP019798.1|WP_030853436.1|5238193_5239465_-|magnesium-transporter	gnl|CDD|225148	COG2239, MgtE, Mg/Co/Ni transporter MgtE (contains CBS domain) [Inorganic ion transport and metabolism].	2.9164e-47
NZ_CP019798.1|WP_078095037.1|5256536_5257520_+|ABC-transporter-permease	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.03973e-74
NZ_CP019798.1|WP_030853457.1|5244929_5245535_+|MarC-family-protein	gnl|CDD|225006	COG2095, MarC, Multiple antibiotic transporter [Intracellular trafficking and secretion].	1.38222e-43
NZ_CP019798.1|WP_060176711.1|5254800_5256540_+|ABC-transporter-substrate-binding-protein	gnl|CDD|173871	cd08506, PBP2_clavulanate_OppA2, The substrate-binding domain of an oligopeptide binding protein (OppA2) from the biosynthesis pathway of the beta-lactamase inhibitor clavulanic acid contains the type 2 periplasmic binding fold. Clavulanic acid (CA), a clinically important beta-lactamase inhibitor, is one of a family of clavams produced as secondary metabolites by fermentation of Streptomyces clavuligeru. The biosynthesis of CA proceeds via multiple steps from the precursors, glyceraldehyde-3-phosphate and arginine. CA possesses a characteristic (3R,5R) stereochemistry essential for reaction with penicillin-binding proteins and beta-lactamases. Two genes (oppA1 and oppA2) in the clavulanic acid gene cluster encode oligopeptide-binding proteins that are required for CA biosynthesis. OppA1/2 is involved in the binding and transport of peptides across the cell membrane of Streptomyces clavuligerus. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	4.07972e-172
NZ_CP019798.1|WP_078095038.1|5257516_5258509_+|ABC-transporter-permease	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	5.23882e-95
NZ_CP019798.1|WP_060176704.1|5243989_5244853_+|PHP-domain-containing-protein	gnl|CDD|223686	COG0613, COG0613, Predicted metal-dependent phosphoesterases (PHP family) [General function prediction only].	1.41907e-45
NZ_CP019798.1|WP_030853473.1|5250880_5251519_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.13882e-14
NZ_CP019798.1|WP_078095034.1|5249216_5249975_+|tRNA-2-methylthio-N6-isopentenyl-adenosine(37)-hydroxylase-MiaE-like-protein	gnl|CDD|205967	pfam13794, MiaE_2, tRNA-(MS[2]IO[6]A)-hydroxylase (MiaE)-like.	1.25652e-87
NZ_CP019798.1|WP_078095032.1|5241106_5242222_-|magnesium-and-cobalt-transport-protein-CorA	gnl|CDD|213364	cd12830, MtCorA-like, Mycobacterium tuberculosis CorA-like subfamily. This bacterial subfamily belongs to the Thermotoga maritima CorA (TmCorA)-like family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subfamily includes the Mg2+ transporter Mycobacterium tuberculosis CorA (which also transports Co2+). Thermotoga maritima CorA forms funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport by a related protein, Saccharomyces cerevisiae Alr1p. Natural variants in this signature sequence may be associated with the transport of different divalent cations. The functional diversity of the MIT superfamily may also be due to minor structural differences regulating gating, substrate selection, and transport.	1.2889e-165

Protein sequences

>NZ_CP019798.1|WP_030853460.1|5245859_5246717_-|alpha/beta-hydrolase
MSKPPRLTLPSAARAYHLSTDRGSFAVHEAGEPVRGTALLVPGFTGSKEDFIGLLEPLAAAGYRVVAVDGRGQHETPGPREESAYGMEELAGDVLAQVRALGAERVHLVGHSLGGLVSRAAVLRDPSPFASLTLLSSGPAAIAEEQQARTKLLVAALEAMGDDMPGIWEAMRAHDAQDAARDSPELTRFLRERWLATVPEQLVVTGRALICEPDRVDELSRVALPKLVLSGAVDYAWPVPLMDAMAERLGARRVVVPGTEHSPNAEDPATTAAALASFWDSATPV
>NZ_CP019798.1|WP_167389209.1|5245611_5245764_-|hypothetical-protein
MRFEILRLDDVDGTAVDSTVVDAASVNRIVQQAASIGQRILIRPAERASS
>NZ_CP019798.1|WP_030853457.1|5244929_5245535_+|MarC-family-protein
MFDFAVFGSLFLTLFVIMDPPGITPIFLALTSGRPVKVQRRMAWQAVCVAFGVIAVFGLCGQQILDYLHVSVPALMIAGGLLLLLIALDLLTGKTDEPKQTKDVNVALVPLGMPLLAGPGAIVSVILAVQKADGAAGQISVWAAIIAMHVVLWITMRYSLVIIRVIKDGGVVLVTRLAGMMLSAIAVQQIINGVLQVVRGS
>NZ_CP019798.1|WP_060176704.1|5243989_5244853_+|PHP-domain-containing-protein
MRIDLHAHSTASDGTDTPAELVRNAAGAGLDVVALTDHDTVGGYGEALAALPAGLTLVTGAELSCRLDGVGVHMLAYLFDPEEPELARERELVRDDRVPRARTMVGKLQDLGVDVTWEQVARIAGDGSVGRPHIATALVELGVVPTVSDAFTPDWLADGGRAYAEKHELDPFDAVRLVKAAGGVTVLAHPAAVKRGRCVSESAIAELAAAGLDGVEVDHMDHDTDTRARLRALAADLGLLTTGSSDYHGSRKTCRLGEYTTDPEIYGEITRRATGAFPVPGAGGRGR
>NZ_CP019798.1|WP_060176703.1|5243242_5243887_+|hypothetical-protein
MRGEPTCPKCGGRVRAPGLFSDSWQCAVHGAVHPLQPVIPPSVEGLGVVVHRARVPVWMPWPLPLGWLFTGVASAGDDRSGGRATVVACSGPGPVGGVGELLLIAEELGVGLGARYAGIDGLDPGRSINMDGPPHTKVVAAGRPTPLWHVGGGPDDRAVFAGEARGLWLWAIVWPQQSGLLLYDELVLTDLREGGAEVELLPCGALSPRILGPV
>NZ_CP019798.1|WP_030853448.1|5242597_5243182_+|suppressor-of-fused-domain-protein
MAEILALVEARLRTAFGEPDARAAVTFLGTDRIEVLRFAEGDLVRYATLGMSANPMTDPTAVVADPVRGPRAELVLTVRGGLADTDKLLRPLAVLAASPQVEGLVVAPGASLDVGEPLWEGAPFSSVLVAEPGGLVEDLELDEPMEAVRFLPLLPMTANEAAWKRVHGAAALQERWLARGTDLRDPLRSAVALD
>NZ_CP019798.1|WP_078095032.1|5241106_5242222_-|magnesium-and-cobalt-transport-protein-CorA
MSMLPYLRAAVRPSLRKSTPVQPGYDATRDPSASSAVVDCAVYRDGRRVLGPACLTPREAIRRVREDGGFAWIGLHEPTEAEFAGIAATFGLHPLAVEDAVHAHQRPKLERYDDTLFTVFKTIHYVEHAELTATSEVVETGEVMCFTGPDFVITVRHGGQGSLKGLRHRLQDDPDLLSKGPSAVLHSIADHVVDGYIAVAAAVQDDIDEVESEVFAAPAKGSARGGDAGRIYQLKREVLEFKRAVSPLLRPMELLSERPMRLVDPDIQKYFRDVADHLARVHEQVVGFDELLNSILQANLAQATVAQNEDMRKITSWAAIIAVPTMICGVYGMNFEHMPELRWEYGYPMVMATIFGACFTIHRALRRHGWL
>NZ_CP019798.1|WP_030853443.1|5240519_5241035_-|hypothetical-protein
MTLSTLDLALVEEATKKSGLIWVRGAGADRALWHAWVDGAAHVLGDGPGEQPFPGLADGAGAEVTVRSKDKGGRLVAWTATVRELPPRGEEWQAAVAELKGKRLNAPDAQDMTERWARECRLLRLEPESVRSALPDGSLAAAPLGSPATTRRPVPAALPKLLLKRRKAARG
>NZ_CP019798.1|WP_037834246.1|5239678_5240443_+|hypothetical-protein
MRRAALIGVLCAGLAVTGTGCGDDPDEGTNGVGRLTADKIEAKAKAAAGDAESVHLSGTLVSGGKAFTVDMRLKSDGGSGEVKSQDDTFQLLRVGEQLYLKASAAFWGQTDSAGKLADKYVKVPEGDPSYKQFRGFTDMDVLLDGLLGLEGKLAKGSYTKVGHTRAVQVTADEGKGGKLSVSLEGTPYPLLMERAGGAGRVELAEWGKPFQLDPPAQDQTVDYGSQLPTTKGEGGAPAPAASKGSGQGANPTTP
>NZ_CP019798.1|WP_030853436.1|5238193_5239465_-|magnesium-transporter
MVAGAPRIFVSHLSGVPVFDPNGDQVGRVRDLVAMLRVGGRPPRLLGLVVEVVSRRRVFLPMTRVTGVESGQVITTGVINMRRFEQRPTERLVLGELLDRRVTLVASGEEVTVLDVAIQQLPARRDWEIDRIFVRKGKSGALRRRGEALTVEWSAVTGFSLEEHGQGAENLVATFEQMRPADVANVLHHLTPKRRAEVANALDDDRLADVLEELPEDEQVEILGKLKEERAADVLEAMDPDDAADLLSELPEDDKERLLTLMRPDDAADVRRLLSYEENTAGGLMTTEPIVLRPDATVADALARVRQADLSPALAAQVYVCRPPDETPTGKYLGTVHFQRLLRDPPFTLVSSIVDTDLPPLRPNASLPAVTTHLAAYNMVAVPVVDESGSLLGAVTVDDVLDHLLPDDWRETEFHSEEAVGGR
>NZ_CP019798.1|WP_078095034.1|5249216_5249975_+|tRNA-2-methylthio-N6-isopentenyl-adenosine(37)-hydroxylase-MiaE-like-protein
MPTVENASPADDSNPAEATGIASQNWAAASASPQYRAAVVDLLGALAYGELAAFERLAEDAKLAPTLDDKAELAAMASAEFHHFERLRDRLTKIEAEPTAAMEPFAQGVDAFHRQTAPSDWLEGLVKAYVGDSIASDFYREVASHLDTDTRALVLGVLDDTGHGNFAVEKVRAAIEADPRCGGRLALWARRLMGEALSQAQRVVAERDALSTMLVGGVDGMAAGFDLAAVGEMFTRITKAHTKRMAALGLAA
>NZ_CP019798.1|WP_060176943.1|5250072_5250372_-|hypothetical-protein
MLMEVLGSALLGLALSAAAVRRLESRLPSRRVVLVSGVLGALFGAYLTRFALGPGHSTLLATLIGAVLVSAVVLSLLLRPARGPRRRPHGAPFSLPSRG
>NZ_CP019798.1|WP_030772789.1|5250484_5250712_-|DUF3107-domain-containing-protein
MEVKIGVQHAPREIVLESDLSAEELESIVSAALSGNEPLLSLTDNKGRKVLVPSDRLSYVDLGEPTTRKVGFGAL
>NZ_CP019798.1|WP_030853473.1|5250880_5251519_-|TetR/AcrR-family-transcriptional-regulator
MTAIEQTEAARPRGTRLPRRARRNQLLGAAQEVFVAQGYHAAAMDDIAERAGVSKPVLYQHFPGKLDLYLALLDQHCEALLLAVRTALASTTDNKLRVAATMDAYFAYVEDEGGAFRLVFESDLTNEPAVRERVDRVSLQCAEAISDVIAEDTGLSKDESMLLAVGLGGVSQVVARYWLSSESPVARETAVGLLTSLAWRGIAGFPLHGTES
>NZ_CP019798.1|WP_078095035.1|5251665_5251881_-|hypothetical-protein
MTVDPAEPDTFRERFAESLDPEAPEADVAEQQADLRPDDDDPDTGREAGQAADGDAAEQARVVQLDEDDYR
>NZ_CP019798.1|WP_076043388.1|5252013_5253009_+|alpha/beta-hydrolase
MSSTELPGVRSAAEPSSPSGAVRLADGEQLRTAALPGLELAVRVRPPRRDGLPPALFVHGLGGSSQNWSALMEQLADTVDGEAVDLPGFGWSPPPADRDYSVTAFARAVIRHLDAAGRGPVHLFGNSLGGAVSTRVAAVRPDLVRTLTLVSPALPELRVQRSAVPTALLALPGVAALFSRMTQGLSAEQRTRGVTDLCYGDPSRVTPEGFRNAVEEMERRMALPYFWDAMTRTSRGIVDAYTLGGQHGLWRQAQRVLAPSLLVYGGRDQLVSYRMAHKAAAAFRGSRLLTLPEAGHVAMMEYPEAVAAAFTELLRDTGAGAAVRDTEDGRG
>NZ_CP019798.1|WP_078095036.1|5253014_5254454_+|DUF3152-domain-containing-protein
MGRHSRKSGAPAPEPAPAPAPSAARPQAQQPDPAAYEDRFAYDASGDDVFGNGDPFAGWPEPTVTHHGYVSQDRPAGSGERAGGHPQQYETGGAWGAGADSVYGDWHGVPRPRFGGDPAPAPAARAAAPPAPRDYDTPAFGTPPVGFPQVTFDQPAPGLPRPRPGRAGPVTSTGSHRLVPGPALPADAVEERPASGRGRKALAYTGMAAAAVTTVLAVVVAGQGFLDTDADEARAGAPAATDKDRSDTAASRSDGRPTRNGGAAVPLAPPAAAPAPAPELTYEQQMAAQLPLDPKLAGPGTFDTVPGVAKAPGKGKIVRYRVDVEQGLGLDPQLFAEAVHRTLNDDRSWGHGGTKTFERVPGGEADFVITLASPGTTGVWCAKSGLDTVVGNVSCDAATTERVMINAFRWAQGSETYGPDQMFAYRQMLINHEVGHRLGHGHVNCRTPGALAPVMQQQTKSLNIDGIQCRPNPWAFPGN
>NZ_CP019798.1|WP_060176711.1|5254800_5256540_+|ABC-transporter-substrate-binding-protein
MSRQSHISRRVAAAAVSLVLAGGAAACGPKDGADAAGAAGGKPGAAGAPQKGGTLTVLNSEPQNDFDPARLYTSGGGNVPSLVFRTLTTRNREDGAAGTKVVPDLATDIGRPNADATEWTYTLKDGLKYEDGSPITTADIKYGIERSFAAELSGGAPYLRDWLVGGESYEGPYKDGGKGLDSIAVPDAKTIVFKLRKPEGEFPFVATQTQFAPVPRAKDTGAKYEEHPLSSGPYKVVGNENDGERLTLERNEHWDQKTDEERKAYPDRIDVRSGLDAAVINQRLTTSAGPDAAAITTDTNLGPAELAQVGDNKELAGRVGTGHFGYVNYIAFNPKVAPFDNPKVRQAISHAINRTSVVNAAGGSALAEPATTFLPEREAFGFTPYDHFPAGKTGDPAKAKELLKEAGFPDGLTVTLTHSTAQNRQTSPEVATAVQQALAAAGITVKLEGLENNAFNERRWDAKNTPGFFLSRWGADWPSGGPFLAPIFDGRQIVTGGSNYNHAQLDDPAVNAEIDEIAKLTDLAAAGKRWGALDKKIGEQALTVPLFHPVYKRLVGKDVKNVVISDWTGVLDISQVAVK
>NZ_CP019798.1|WP_078095037.1|5256536_5257520_+|ABC-transporter-permease
MSLTLERSAPAPGAVPRGAGAGRQVWRRLRRRPSAAVAAAVLALLVLLALAAPLVAHLTGQDPNTYHDDLVDSARGGVPIGSFGGISADHWLGVEPGTGRDLFTRLLYGARVSLLVALGAVAVQTAVGVAVGLAAALGGRTADQVIGRTTDVMIALPMLVIGIALTAVVPPDFPRPLLLVLIIGLLDWGGTARMVRAQALALRGLDFVDAARLAGSGKLRIARRELLPSLAAPVITYAAIKVPTAIVAEASLSFLGVGVKPPTPSWGQMLSSAQTWFRADPAYVLLPAGLLFTTVLASTVLGDAVRTALDPREGSRLRVGTGKERTG
>NZ_CP019798.1|WP_078095038.1|5257516_5258509_+|ABC-transporter-permease
MTRFVLKRTGGALLVLLALSVIVYSLFYLAPGDPARLACGERCTPQQIAQVREQLGLNESTVAQYLHFLQGLVAGRDHSAGAGLVLHCDAPCLGLSYQTDQQVTDLILTRLPATLSLALGALAIWLLVGVGTGVLSALRRGGITERLLTVLTLAGTGTPVFILGLLLLMAVCAYLQWLPFPTYVPLTEDPEQWAWNLLLPWLTLGLFESAKYARITRSSTLETLAEDHIRTFRAYGVGERALVTRHAVRGAVAPVIALSAVDFGTMIGGAVLTESLFGIPGLGKTLIDAVRVVDLPVVVGVVLAIGTAVVVAGAVADLLYAAADRRVALA

Crispr_ID: NZ_CP019798_11

• CRISPR_ID: NZ_CP019798_11
• CRISPR_location: 5576157-5576259
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_11

Consensus_repeat	Method
GGCGGAGCCCCGCATTCCGCCGAGCCCGC	CRISPRCasFinder

spacers of NZ_CP019798_11

>11.1|5576186|45|NZ_CP019798|CRISPRCasFinder
AGGGCCGAACCCGGCCTCGGCGGCGCTGGGTTACCCGCAGCCGGC

CRISPR arrays and Neighbor proteins around NZ_CP019798_11

CRISPR arrays

The CRISPR arrays of NZ_CP019798_11

>merge|NZ_CP019798|11|5576157-5576259|CRISPRCasFinder
GGCGGAGCCCCGCATTCCGCCGAGCCCGCAGGGCCGAACCCGGCCTCGGCGGCGCTGGGTTACCCGCAGCCGGCGGCGGAGCCCCGCACTCCGCCGAGCCCGC

>NZ_CP019798|11|7|5576157-5576259|CRISPRCasFinder
GGCGGAGCCCCGCATTCCGCCGAGCCCGC	AGGGCCGAACCCGGCCTCGGCGGCGCTGGGTTACCCGCAGCCGGC
GGCGGAGCCCCGCACTCCGCCGAGCCCGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078095124.1|5583658_5584612_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078095123.1|5583314_5583659_+|DUF1330-domain-containing-protein	unknown	unknown	gnl|CDD|377765
NZ_CP019798.1|WP_030846801.1|5576401_5577058_+|trimeric-intracellular-cation-channel-family-protein	unknown	unknown	gnl|CDD|225415
NZ_CP019798.1|WP_030846804.1|5577104_5577959_+|thioesterase-family-protein	unknown	unknown	gnl|CDD|379298
NZ_CP019798.1|WP_078095121.1|5578079_5579243_+|cysteine-desulfurase	unknown	unknown	gnl|CDD|224029
NZ_CP019798.1|WP_060176830.1|5567575_5568310_+|enhanced-serine-sensitivity-protein-SseB	unknown	unknown	gnl|CDD|379654
NZ_CP019798.1|WP_078095122.1|5581131_5582055_-|NADP-dependent-oxidoreductase	unknown	unknown	gnl|CDD|176191
NZ_CP019798.1|WP_030846814.1|5579991_5581122_+|tRNA-2-thiouridine(34)-synthase-MnmA	unknown	unknown	gnl|CDD|234664
NZ_CP019798.1|WP_060176958.1|5582191_5583220_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|181818
NZ_CP019798.1|WP_030846773.1|5564722_5565103_-|glycine-cleavage-system-protein-GcvH	unknown	unknown	gnl|CDD|234918
NZ_CP019798.1|WP_030846793.1|5570679_5572458_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173871
NZ_CP019798.1|WP_030846791.1|5569609_5570605_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224094
NZ_CP019798.1|WP_030846786.1|5568405_5569146_+|enhanced-serine-sensitivity-protein-SseB-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|379654
NZ_CP019798.1|WP_030846777.1|5565206_5566322_-|glycine-cleavage-system-aminomethyltransferase-GcvT	unknown	unknown	gnl|CDD|234742
NZ_CP019798.1|WP_051700252.1|5574715_5575822_+|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|236898
NZ_CP019798.1|WP_078095120.1|5573585_5574719_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_CP019798.1|WP_076042916.1|5584756_5585446_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|181298
NZ_CP019798.1|WP_078096327.1|5566802_5567462_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|379324
NZ_CP019798.1|WP_030846795.1|5572590_5573589_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP019798.1|WP_030846810.1|5579256_5579922_-|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl|CDD|376556

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_078095123.1|5583314_5583659_+|DUF1330-domain-containing-protein	gnl|CDD|377765	pfam07045, DUF1330, Domain of unknown function (DUF1330). This family consists of several hypothetical bacterial proteins of around 90 residues in length. The function of this family is unknown.	4.72814e-28
NZ_CP019798.1|WP_030846801.1|5576401_5577058_+|trimeric-intracellular-cation-channel-family-protein	gnl|CDD|225415	COG2860, COG2860, Predicted membrane protein [Function unknown].	2.19007e-50
NZ_CP019798.1|WP_030846804.1|5577104_5577959_+|thioesterase-family-protein	gnl|CDD|379298	pfam13622, 4HBT_3, Thioesterase-like superfamily. This family contains a wide variety of enzymes, principally thioesterases. These enzymes are part of the Hotdog fold superfamily.	3.87712e-45
NZ_CP019798.1|WP_078095121.1|5578079_5579243_+|cysteine-desulfurase	gnl|CDD|224029	COG1104, NifS, Cysteine sulfinate desulfinase/cysteine desulfurase and related enzymes [Amino acid transport and metabolism].	1.19712e-163
NZ_CP019798.1|WP_060176830.1|5567575_5568310_+|enhanced-serine-sensitivity-protein-SseB	gnl|CDD|379654	pfam14581, SseB_C, SseB protein C-terminal domain. This family consists of several SseB proteins which appear to be found exclusively in Enterobacteria. SseB is known to enhance serine-sensitivity in Escherichia coli and is part of the Salmonella pathogenicity island 2 (SPI-2) translocon. This presumed domain is found at the C-terminus of SseB proteins.	5.32515e-28
NZ_CP019798.1|WP_078095122.1|5581131_5582055_-|NADP-dependent-oxidoreductase	gnl|CDD|176191	cd05289, MDR_like_2, alcohol dehydrogenase and quinone reductase-like medium chain degydrogenases/reductases. Members identified as zinc-dependent alcohol dehydrogenases and quinone oxidoreductase. QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR actin the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. 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.	8.46728e-126
NZ_CP019798.1|WP_030846814.1|5579991_5581122_+|tRNA-2-thiouridine(34)-synthase-MnmA	gnl|CDD|234664	PRK00143, mnmA, tRNA-specific 2-thiouridylase MnmA; Reviewed.	0
NZ_CP019798.1|WP_060176958.1|5582191_5583220_+|helix-turn-helix-domain-containing-protein	gnl|CDD|181818	PRK09393, ftrA, transcriptional activator FtrA; Provisional.	2.2896e-104
NZ_CP019798.1|WP_030846773.1|5564722_5565103_-|glycine-cleavage-system-protein-GcvH	gnl|CDD|234918	PRK01202, PRK01202, glycine cleavage system protein GcvH.	1.67703e-55
NZ_CP019798.1|WP_030846793.1|5570679_5572458_+|ABC-transporter-substrate-binding-protein	gnl|CDD|173871	cd08506, PBP2_clavulanate_OppA2, The substrate-binding domain of an oligopeptide binding protein (OppA2) from the biosynthesis pathway of the beta-lactamase inhibitor clavulanic acid contains the type 2 periplasmic binding fold. Clavulanic acid (CA), a clinically important beta-lactamase inhibitor, is one of a family of clavams produced as secondary metabolites by fermentation of Streptomyces clavuligeru. The biosynthesis of CA proceeds via multiple steps from the precursors, glyceraldehyde-3-phosphate and arginine. CA possesses a characteristic (3R,5R) stereochemistry essential for reaction with penicillin-binding proteins and beta-lactamases. Two genes (oppA1 and oppA2) in the clavulanic acid gene cluster encode oligopeptide-binding proteins that are required for CA biosynthesis. OppA1/2 is involved in the binding and transport of peptides across the cell membrane of Streptomyces clavuligerus. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP019798.1|WP_030846791.1|5569609_5570605_+|ABC-transporter-permease	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.73676e-92
NZ_CP019798.1|WP_030846786.1|5568405_5569146_+|enhanced-serine-sensitivity-protein-SseB-C-terminal-domain-containing-protein	gnl|CDD|379654	pfam14581, SseB_C, SseB protein C-terminal domain. This family consists of several SseB proteins which appear to be found exclusively in Enterobacteria. SseB is known to enhance serine-sensitivity in Escherichia coli and is part of the Salmonella pathogenicity island 2 (SPI-2) translocon. This presumed domain is found at the C-terminus of SseB proteins.	3.10957e-24
NZ_CP019798.1|WP_030846777.1|5565206_5566322_-|glycine-cleavage-system-aminomethyltransferase-GcvT	gnl|CDD|234742	PRK00389, gcvT, glycine cleavage system aminomethyltransferase GcvT.	0
NZ_CP019798.1|WP_051700252.1|5574715_5575822_+|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	2.37841e-152
NZ_CP019798.1|WP_078095120.1|5573585_5574719_+|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.85881e-174
NZ_CP019798.1|WP_076042916.1|5584756_5585446_+|SDR-family-oxidoreductase	gnl|CDD|181298	PRK08219, PRK08219, SDR family oxidoreductase.	1.66826e-107
NZ_CP019798.1|WP_078096327.1|5566802_5567462_+|AAA-family-ATPase	gnl|CDD|379324	pfam13671, AAA_33, AAA domain. This family of domains contain only a P-loop motif, that is characteristic of the AAA superfamily. Many of the proteins in this family are just short fragments so there is no Walker B motif.	3.7549e-06
NZ_CP019798.1|WP_030846795.1|5572590_5573589_+|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	6.47814e-101
NZ_CP019798.1|WP_030846810.1|5579256_5579922_-|N-acetylmuramoyl-L-alanine-amidase	gnl|CDD|376556	pfam01510, Amidase_2, N-acetylmuramoyl-L-alanine amidase. This family includes zinc amidases that have N-acetylmuramoyl-L-alanine amidase activity EC:3.5.1.28. This enzyme domain cleaves the amide bond between N-acetylmuramoyl and L-amino acids in bacterial cell walls (preferentially: D-lactyl-L-Ala). The structure is known for the bacteriophage T7 structure and shows that two of the conserved histidines are zinc binding.	4.85813e-37

Protein sequences

>NZ_CP019798.1|WP_051700252.1|5574715_5575822_+|dipeptide-ABC-transporter-ATP-binding-protein
MTDTKKTDPAVTLPAQATDSPEPLLKVTGLTKHFPITKGLLRRQSGAVKAVDGLDFDVRRGETLGVVGESGCGKSTMGRLITRLLEPTGGTIEFEGKDITHLGVAGMRPLRRDVQMIFQDPYGSLNPRHTVGTIVSAPFKLQNVTPEGGLKAEVQRLLSLVGLNPEHYNRYPHEFSGGQRQRIGIARALALKPKLVVADEPVSALDVSIQAQVVNLLDDLQQELGLTYVIIAHDLSVIRHVSDRIAVMYLGKIVELADNKSLYGEPMHPYTTALMSAVPVPDPRRRGAKSGRILLKGDVPSPISPPSGCRFHTRCWKATQICATQEPPLLALKTGHQVACHHPENAPDQAPDDKPLPGAADAVTTATD
>NZ_CP019798.1|WP_078095120.1|5573585_5574719_+|ABC-transporter-ATP-binding-protein
MTDPTTKTGETGETRALNQPYDGAPSPTAFLDVRDLKVHFPTEDGLVKSVDGLSFTLEKGRTLGIVGESGSGKSVTSLGIMGLHRVGQYGRQRARISGEIWLDGKELLSADEDEVRRLRGREIAMIFQDPLSAMHPYFTVGKQISEAYRVHHKVDKKAARKRAVELLDRVGIPEPHKRFDSYPHEFSGGMRQRAMIAMALVNNPELLIADEPTTALDVTVQAQILDLIRDLQKEFGSAVIMITHDLGVVAEMADELLVMYGGRCVERGTAEKVFYEPRHPYTWGLLGSMPRIDREQTERLIPVKGSPPSLINIPSGCAFNPRCPYADVPKGNVTRTVRPELTAQDDTGQDGTRHWSACHMSQEERTRIWTEEIAPKL
>NZ_CP019798.1|WP_030846795.1|5572590_5573589_+|ABC-transporter-permease-subunit
MLAYLIRRIFAVLVMLLVITLVTFGIFFLFPKLIGTDPALYFVGKQSDPAAIEGIRQKMGLDDPILVQFGKFVVGLVAGRTYANGSDVTQCAAPCFGYSFKTEQEVWPLLLDWLPVTLSLAMGAVVLWVAGGVATGVVSALKRGSLLDRSAMGVALAGVSLPIYFTGMLVIALFSDQLGWFGRPEASFAEDPGRWFNGMILPWVSLAFLYAAMYARLTRATMLEVLGEDYIRTARAKGLTEPVVIGKHAMRSTMTPILTVLGLDLGALMGGAVLTEYTFSLHGLGYSAVRAISEHDLPVILGITLISAFFVVAANLIVDLLYAVIDPRVRLS
>NZ_CP019798.1|WP_030846793.1|5570679_5572458_+|ABC-transporter-substrate-binding-protein
MTTHRTSKRRLAAGTAVVLAAMLTATACGGAEKKDDKAAASGSGFNAGIDKVANASDKKGGELKFVGTQDADSWDPQRGYYGFMWDFSRYYTRQLISFKPGPGKESTELVPDLATAKAEISDGGKTYKYTLKDNVTWEDGSPVTAQDVKYGIERTWAQDVISGGPVYLQQVLDPKAEYPGPYKDTAPDKLGLKAIETPDAKTIIFKLPTPNGDFEQMLAMPAASPVKQDKDTAAKYGLKPFSNGPYKIDSYEPNKSMKLSRNENYKPESDTIRKALPDTISVTFMANADDMDKRLMNGEFDLDINATGIGQAARATALKDHKGNLDNGQTGFIRYAVMPQTVAPFDNIECRKAVIYAADKKSLQTARGGPQAGGDIAPNMLPLGIKGSDAKYDPYEVLKNDGKPNLEKAKEALKACGKETGFKTTIAVRNNKPVEVATAVSLQNALKQVGIEADVDQFDGAQTSGIIGSPKVVKEKGYGIIIMGWGADFPTGQGFSQPLVDGRFILQSGNNNFSELNDPAINSLFDQAIAETDPTKAGDIYKQMNQKVSEAAVYLPFVYDKTITWRSSRLTNAYTTDAYNGRYDYASLGVVK
>NZ_CP019798.1|WP_030846791.1|5569609_5570605_+|ABC-transporter-permease
MTAPLHDTSAAEPAAVAAPDVPQKAIEGRSPWQIAWLRLKRDKVALAGGIIVILLILVAIFAPLIVKAFGHPPEELHEDLLDPLLGLPLGDWGGMSSDFLLGVEPVNGRDVFSRIVYGARISLLVAFLSAFVAVSLGTVFGIVAGYFGGWVDAAISRVMDLLLAFPQLLFIIALISVIPNKLWGFEGSGLRIAVLVLVIGFFGWPYIGRIVRGQTLSLREREYVEAARSLGAGRFYILFRELLPNLVAPITVYATLMIPTNVLTEAALSFLGVGVKPPTPSWGETLATAVRTYEDDPLFMIFPGVAIFITVLAFNLFGDGVRDALDPKGSR
>NZ_CP019798.1|WP_030846786.1|5568405_5569146_+|enhanced-serine-sensitivity-protein-SseB-C-terminal-domain-containing-protein
MSASGTAAAGQVEHMMRQVTPGRYESYESLLHALSEGRLWMLLWQGQPGSPDAQYGGMEVEGLGYAPCVTSPQELAASGWNRGYEVVTGRDIARALYPDRWGLWLNPHAQGGGLGVPWADLRRIATGLDRMPAGPLRLSEPSIELPQFYGLLTQHAHRTPAVRSLRRAWVQPALGSPYLAVGLDLYDASGPALESVREMMRQSVGAVPEGVPVCTVALADEHDPVAMWLRAQTRPFYDREGQAPAY
>NZ_CP019798.1|WP_060176830.1|5567575_5568310_+|enhanced-serine-sensitivity-protein-SseB
MQGSGWPGNELEQVLGAALGQPDAGGRILEVLGRSQVWVPLPGGGGPDTAGLDLPTMDIGGAAYVPVYSSEAQFLACVGPGMDFAVAPAVEFARGLPPQLGIAVNPEGAVGVPLPPPAVAELCRAGRSPLDGPAAGGRVRLFEPDWQEDPVDFLAAAGEEFRATGVVAAAHRCLASVEGGAPQLFIGVRLAGWEPQLREAPMEALGRALARVPAPWPVQLILLDAAQDPVTDWIRERVRPFYLP
>NZ_CP019798.1|WP_078096327.1|5566802_5567462_+|AAA-family-ATPase
MTTTGTVEAVPGQRRGARDRRRAADGGLGLVRDLRGPALTAPRRLGFAEGDIVVVSGLPGGGKSTLIKRAAPEGGAVDSQDTRERWERRMPARLPYAVYRPLVRAAHYWGLYRILRSGASVVVHDCGTQSWVRGLLAAAARRRGRALHLVLLDSSPEEALSGQAARGRGVSAYAFARHRGAVGRLLRDAEEGRPPAGCASATLLDRRSAAAVTGIGFHP
>NZ_CP019798.1|WP_030846777.1|5565206_5566322_-|glycine-cleavage-system-aminomethyltransferase-GcvT
MSTAPRLTALDALHRSLGATMTDFAGWDMPLRYASERDEHNAVRTKAGLFDLSHMGEITLTGPEAVKALDYALVGNISTVGVGRARYTHICQEDGGILDDLIVYRLGETEYMVVANASNAQVVLDALTERAAGFDTEVRDDRDAYALIAVQGPESPGILASLTDADLDGLKYYAGLPGTVAGVPALIARTGYTGEDGFELFVAPEHAVELWQALAKAGEGVGLVPAGLSCRDTLRLEAGMPLYGHELTTSLTPFDAGLGRVVKFEKEGDFVGRAALEAAAEKAASQAPRKLVGLVAEGRRVPRAGFPVVAGGKVVGEVTSGAPSPTLGKPIAMAYVDAEHAAPGTSGVGVDIRGTHEPYEVVALPFYKRQK
>NZ_CP019798.1|WP_030846773.1|5564722_5565103_-|glycine-cleavage-system-protein-GcvH
MSNPEKLRYTKEHEWLSDVVDGVATVGITEFAANALGDVVYAQLPEVGDTVTEGETCGELESTKSVSDLYSPVSGEIVEANQDVVDDPALVNTAPFEGGWLFKVRLSEEPKDALSFEEYTKLTAGN
>NZ_CP019798.1|WP_030846801.1|5576401_5577058_+|trimeric-intracellular-cation-channel-family-protein
MLHDLFPPGVQHALDLAGIFVFATSGALLAVRKNFDVFGIAVLALVTALGGGLFRDLVIGAVPPAAFGELSFFVTPLLAAAFVFFLHPEVQRINRAINVFDAAGLALFCVTGTTKAYEYGLGLTASAALGLATAVGGGVLRDVLVNEVPSLLRDREMYAVPATVGAAMVAVSIALDSLNAVTTGLAIVTTFVLRLLAMRYHWRAPLAWNRRSSVAEEP
>NZ_CP019798.1|WP_030846804.1|5577104_5577959_+|thioesterase-family-protein
MSYAAAQASIGDSEFDRDTAITERAGEPGVYDAELSAGWTIIAAVNGGYLLALVGRALSATLPHPDPFTVSAHYLTSSVPGPAVIRTEVVRVGRTLSTGQASLLQYDEHGNEVERIRVLASYGDLASLPDDVRTVAEPPLMPSYENCVGPEAGPAPIPGSSAIVDRLRLRLDPATAGWAVGAPSGKGEMRAWFELADGRDADPLSMLLAVDALPPTAFDLGLVAWTPTVELTTHIRRRPAPGPLRISITTRNLAGGFLEEDAEVWDSTDHLVAQSRQLARALRI
>NZ_CP019798.1|WP_078095121.1|5578079_5579243_+|cysteine-desulfurase
MAYLDHAATTPMLPEAAAAMTAQFAATGNASSLHAAGRRARRTVEEAREAFAEAIGARPSEVVFTAGGTEADNLAVKGLYWARRDADPARTRVIASPVEHHAVLDAVHWLAEHEGAQVDYLPVDRYGRVHPDAFREAVERNPDDVALATVMWANNEIGTVMPVRELAATAREAGIPLHSDAVQAFGQLDVYFADSGLAAMTVSGHKIGGPYGIGALLLGRDQSPVPVLHGGGQERHVRSGTLDVPAVAAFAVAAVLAAERREQFAAEIGALRDELIAAVLAAVPDAVLGGDPEERLPANAHFSFPGCEGDSLLLLLDAQGIECSTGSACTAGVAQPSHVLLAAGTDPRLARGTLRFSLGHTSTKEDVAALAAAIGPAVERARTAGLS
>NZ_CP019798.1|WP_030846810.1|5579256_5579922_-|N-acetylmuramoyl-L-alanine-amidase
MTEQGNTGSKPRSRTRRAVLFGGLGVVAAAAVAGRDEISRTWWLLPGVAKPRKEGEIDHAGAGWTAASPANWRMADRPDDYRVDRIVVHVTQGGFKSSVDAFKNPWHKASAHYIVRGDGHVEQMVRELDVAFHAGNRSMNERSVGIEHVGFVDRPKDFTDAMYAASARLAADICRRYDFPADRGHIVGHSEVPGADHTDPGDHWDWDRYIRMVREALAASA
>NZ_CP019798.1|WP_030846814.1|5579991_5581122_+|tRNA-2-thiouridine(34)-synthase-MnmA
MTENLPRTDRPLRVLAAMSGGVDSAVAAARAVEAGHDVTGVHLALSANPQSFRTGARGCCTIEDSRDARRAADVIGIPFYVWDLAERFREDVVEDFISEYEAGRTPNPCLRCNEKIKFAALLDKALALGFDAVCTGHYATVVLKEDGSRELHRASDMAKDQSYVLGVLDEKQLAHALFPLGDTLTTKEEIRAEAEARGLAVAKKPDSHDICFIADGDTQGFLAHRLGKAEGDIVDESGEKIGTHDGAFGFTIGQRKGLRIGHPAPDGKPRYVLDISPVNNTVTVGPAEALDVSALTAIRPRWCGAEAAAPGTYTAQLRAHGGETEVFAEVVDGELRVSFTEPVRGVAPGQAIVLYDGTRVVGSATIATTTRAAAAV
>NZ_CP019798.1|WP_078095122.1|5581131_5582055_-|NADP-dependent-oxidoreductase
MRAIVVNEWGGPENLVEREIERPEPGLGEVLVRVHAAGVNPVDWKTRASGALIAWGETPILGWDVSGTVEAVGPGVTLYAPGDEVYGMPHFPRQAGGYAEYVAAPARHFARKPASLDHVQAAALPLAALTAWQALVDTAGVTAGQRVLVHAAAGGVGHLAVQIAKARGAYVIGTASAAKHDVLRGLGADELIDYRSVDFAEAVSDVDVVLDALGGDTAERSLKVLRSGGHLISLPGPDSVPADADGVNAAWVLVDPDLKGLEAIADLADRGLLKPLVETVLPLADAARAHEIGEQGRTTGKIVLTVV
>NZ_CP019798.1|WP_060176958.1|5582191_5583220_+|helix-turn-helix-domain-containing-protein
MREDHEQAADTNRRGNGADGRHLVAVLALPGFPPFELGIPSRVFGSAVDDDGDALYEVVVCTADGAPVPSDCGFSLRPAAGPEALAAADTVIVPPTHAMPELARGGPLPPAVAEAIAGIRPGTRLVSICSGSYVLAAAGLLDDRPATTHWNLADEFRRAYPRVRIDEDVLFVDDGDVLTSAGVSAGVDLCLHLIRRDHGVAVTNRAARMCVVPPWRDGGQAQFIDRPVPEPTVATTTATRAWALERLAEPVSLAELAAHARMSLRTFTRRFRDEVGMTPVQWLTAQRLETARHLLESSDLPVDLVAHRSGFGSAGSLRQHMRASLGVSPIAYRRTFRPAAPA
>NZ_CP019798.1|WP_078095123.1|5583314_5583659_+|DUF1330-domain-containing-protein
MTAYAIAHLRPETMNEDILTYIEAIQPTMDAFGGRFLVHGKEVEVLEGPFPGTVVVIGFPDIEQARAWYASDAYQAILPLRTRHIAGEAVLVEGVPADYDASKTAARLRAEAGL
>NZ_CP019798.1|WP_078095124.1|5583658_5584612_+|hypothetical-protein
MGNPATFVIAGSEGYERRSSSFGAVGLDLDLLGGPEAVLPFVLGHRLAEDPWYDDDMCEAGALIDPARKLLLVFAQEGPSVAMRTRAAWLRMLGPAWPGWEVRWTYDGQSGLRTHLGLDPGHVPATVHPGPALAADEEELADPDPMAAVVTVGSGRCHVLAHIADHPVAEGPALLERLADAPAHTGYAGRAEAGIHLDPAARRVGWWLTGIVPHAGRMAARWPGWTVEFWADRWDEHERASGGRFAPPAPDRAAAPADVRAQALQRWAGPRGDVRERLVAALPHARIGHGFAPAVTAEQAAAARAAVERACAAAAGT
>NZ_CP019798.1|WP_076042916.1|5584756_5585446_+|SDR-family-oxidoreductase
MATHLITGAGSGIGAAVATRLHARGDDLVLLARDAARGKQLVERYPGSRALVGDLADPDRLSWAFSKQAVPERIDSLLHIAGIVDLGPVGDLRPKTWHQQLNVNLIAPAEVTRLLLPTLRASKATVVFVNSGAGLNAHADWSAYAASKHGLKALADSLRAEERANGVRVTSVYPGRTASPMQAKVHSQEGKEYDPNDWIDPESVATTILMAVDLPRDAEVNDLTVRPGR

Crispr_ID: NZ_CP019798_12

• CRISPR_ID: NZ_CP019798_12
• CRISPR_location: 6419202-6419299
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_12

Consensus_repeat	Method
GCACCGCCGGGCCAGGGCAAAGGC	CRISPRCasFinder

spacers of NZ_CP019798_12

>12.1|6419226|50|NZ_CP019798|CRISPRCasFinder
CCCGCCCGGCCAGGGCAGAGGCGGCCACCGGCCCGCACCCGGAACCCCCC

CRISPR arrays and Neighbor proteins around NZ_CP019798_12

CRISPR arrays

The CRISPR arrays of NZ_CP019798_12

>merge|NZ_CP019798|12|6419202-6419299|CRISPRCasFinder
GCACCGCCGGGCCAGGGCAAAGGCCCCGCCCGGCCAGGGCAGAGGCGGCCACCGGCCCGCACCCGGAACCCCCCGCACCGCCCGGCCAGGGCAAAGGC

>NZ_CP019798|12|8|6419202-6419299|CRISPRCasFinder
GCACCGCCGGGCCAGGGCAAAGGC	CCCGCCCGGCCAGGGCAGAGGCGGCCACCGGCCCGCACCCGGAACCCCCC
GCACCGCCCGGCCAGGGCAAAGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_030856055.1|6416458_6416638_-|hypothetical-protein	unknown	unknown	gnl|CDD|226202
NZ_CP019798.1|WP_078095367.1|6411546_6412674_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270271
NZ_CP019798.1|WP_030853776.1|6428236_6429403_+|ribosome-small-subunit-dependent-GTPase-A	unknown	unknown	gnl|CDD|234988
NZ_CP019798.1|WP_060180890.1|6416634_6418341_-|nitrite/sulfite-reductase	unknown	unknown	gnl|CDD|223233
NZ_CP019798.1|WP_078095373.1|6432092_6432575_-|DUF456-domain-containing-protein	unknown	unknown	gnl|CDD|377293
NZ_CP019798.1|WP_078095368.1|6421562_6423206_-|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|183199
NZ_CP019798.1|WP_030856072.1|6423223_6424339_+|YihY/virulence-factor-BrkB-family-protein	unknown	unknown	gnl|CDD|377085
NZ_CP019798.1|WP_030856051.1|6415152_6415698_-|adenylyl-sulfate-kinase	unknown	unknown	gnl|CDD|238985
NZ_CP019798.1|WP_078095366.1|6410717_6411512_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224041
NZ_CP019798.1|WP_159425595.1|6425267_6427700_-|VCBS-repeat-containing-protein	unknown	unknown	gnl|CDD|238871
NZ_CP019798.1|WP_078095372.1|6431348_6431966_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_CP019798.1|WP_078095371.1|6429570_6431217_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_158076142.1|6418480_6418657_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078095369.1|6424538_6425012_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP019798.1|WP_051700853.1|6419931_6421194_-|GAF-domain-containing-protein	unknown	unknown	gnl|CDD|225822
NZ_CP019798.1|WP_078095365.1|6409846_6410731_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223673
NZ_CP019798.1|WP_060180888.1|6412865_6414215_-|50S-ribosome-binding-GTPase	unknown	unknown	gnl|CDD|180120
NZ_CP019798.1|WP_030856062.1|6419362_6419926_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP019798.1|WP_030856053.1|6415733_6416462_-|phosphoadenylyl-sulfate-reductase	unknown	unknown	gnl|CDD|234997
NZ_CP019798.1|WP_030856049.1|6414217_6415156_-|sulfate-adenylyltransferase-subunit-CysD	unknown	unknown	gnl|CDD|235375

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_030856055.1|6416458_6416638_-|hypothetical-protein	gnl|CDD|226202	COG3677, COG3677, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	0.00502941
NZ_CP019798.1|WP_078095367.1|6411546_6412674_-|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.	6.38057e-53
NZ_CP019798.1|WP_030853776.1|6428236_6429403_+|ribosome-small-subunit-dependent-GTPase-A	gnl|CDD|234988	PRK01889, PRK01889, GTPase RsgA; Reviewed.	6.47349e-178
NZ_CP019798.1|WP_060180890.1|6416634_6418341_-|nitrite/sulfite-reductase	gnl|CDD|223233	COG0155, CysI, Sulfite reductase, beta subunit (hemoprotein) [Inorganic ion transport and metabolism].	1.10028e-170
NZ_CP019798.1|WP_078095373.1|6432092_6432575_-|DUF456-domain-containing-protein	gnl|CDD|377293	pfam04306, DUF456, Protein of unknown function (DUF456). This family is a putative membrane protein that contains glycine zipper motifs.	5.88193e-19
NZ_CP019798.1|WP_078095368.1|6421562_6423206_-|acyl-CoA-dehydrogenase-family-protein	gnl|CDD|183199	PRK11561, PRK11561, isovaleryl CoA dehydrogenase; Provisional.	3.12847e-170
NZ_CP019798.1|WP_030856072.1|6423223_6424339_+|YihY/virulence-factor-BrkB-family-protein	gnl|CDD|377085	pfam03631, Virul_fac_BrkB, Virulence factor BrkB. This family acts as a virulence factor. In Bordetella pertussis, BrkB is essential for resistance to complement-dependent killing by serum. This family was originally predicted to be ribonuclease BN, but this prediction has since been shown to be incorrect.	8.11372e-44
NZ_CP019798.1|WP_030856051.1|6415152_6415698_-|adenylyl-sulfate-kinase	gnl|CDD|238985	cd02027, APSK, Adenosine 5'-phosphosulfate kinase (APSK) catalyzes the phosphorylation of adenosine 5'-phosphosulfate to form 3'-phosphoadenosine 5'-phosphosulfate (PAPS). The end-product PAPS is a biologically "activated" sulfate form important for the assimilation of inorganic sulfate.	2.45042e-81
NZ_CP019798.1|WP_159425595.1|6425267_6427700_-|VCBS-repeat-containing-protein	gnl|CDD|238871	cd01833, XynB_like, SGNH_hydrolase subfamily, similar to Ruminococcus flavefaciens XynB. Most likely a secreted hydrolase with xylanase activity. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	6.73424e-52
NZ_CP019798.1|WP_078095372.1|6431348_6431966_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.05343e-06
NZ_CP019798.1|WP_078095366.1|6410717_6411512_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224041	COG1116, TauB, ABC-type nitrate/sulfonate/bicarbonate transport system, ATPase component [Inorganic ion transport and metabolism].	1.45448e-110
NZ_CP019798.1|WP_078095369.1|6424538_6425012_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	2.3614e-06
NZ_CP019798.1|WP_051700853.1|6419931_6421194_-|GAF-domain-containing-protein	gnl|CDD|225822	COG3284, AcoR, Transcriptional activator of acetoin/glycerol metabolism [Secondary metabolites biosynthesis, transport, and catabolism / Transcription].	3.09597e-39
NZ_CP019798.1|WP_078095365.1|6409846_6410731_-|ABC-transporter-permease	gnl|CDD|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	2.51658e-53
NZ_CP019798.1|WP_060180888.1|6412865_6414215_-|50S-ribosome-binding-GTPase	gnl|CDD|180120	PRK05506, PRK05506, bifunctional sulfate adenylyltransferase subunit 1/adenylylsulfate kinase protein; Provisional.	0
NZ_CP019798.1|WP_030856062.1|6419362_6419926_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.68459e-10
NZ_CP019798.1|WP_030856053.1|6415733_6416462_-|phosphoadenylyl-sulfate-reductase	gnl|CDD|234997	PRK02090, PRK02090, phosphoadenylyl-sulfate reductase.	2.03734e-114
NZ_CP019798.1|WP_030856049.1|6414217_6415156_-|sulfate-adenylyltransferase-subunit-CysD	gnl|CDD|235375	PRK05253, PRK05253, sulfate adenylyltransferase subunit CysD.	0

Protein sequences

>NZ_CP019798.1|WP_158076142.1|6418480_6418657_-|hypothetical-protein
MTRFRHEWSWNCLGESAARRPRPHVQRHLSGVLTEPATAAHRRNPGIAAVEVSIIAVP
>NZ_CP019798.1|WP_060180890.1|6416634_6418341_-|nitrite/sulfite-reductase
MAATPETPAPAAAAAARRKTGRHRGEGQWAVGHHTPLNGNEQFKKDDDGLNVRTRIETIYAHRGFDSIDPNDLRGRMRWWGLYTQRKPGIDGGKTAILEPEELDDKYFMLRVRIDGGRLTTEQLRVIGEISEEFARGTADLTDRQNVQYHWIRIEDVPEIWRRLEAVGLSTTEACGDTPRVILGSPVAGIAQDEIIDGTPAIDEIYRRIVGNKDFSNLPRKFKSAISGSPLLDVAHEINDIAFVGVNHPEHGPGFDVWVGGGLSTNPKLGVRLGTWVSLDEVPDVYEGVISIFRDYGYRRLRTRARLKFLVADWGAAKFRQVLEDEYLKRKLTDGPAPEQPSGQWRDHVGVHQQQDGRFYVGFAPRVGRVDGATLTKIADIAEQHGSGRLRTTAEQKMIVLDIEGDKVDSVVEALEALDLRVKPSPFRRGTMACTGIEFCKLAIVETKARGASLIDELERRLPDFAEPITININGCPNACARIQVADIGLKGQLVLDDDGNQVEGYQVHLGGALGLEAGFGRKVRGLKVTSAGLPDYVERVVKSYEEQREDGERFAAWVARADEKSLS
>NZ_CP019798.1|WP_030856055.1|6416458_6416638_-|hypothetical-protein
MSERAAPFYCPYCGDEDLFPHETGHGAWECRACNRAFQLKYLGLLARGVQSGPAGGDEI
>NZ_CP019798.1|WP_030856053.1|6415733_6416462_-|phosphoadenylyl-sulfate-reductase
MTTTQDASLKNAALKAATLKELAEQAGRDLEDASAQDILRWAADTFGGKFAVTSSMEDAVVAHLASRVFPGVDVVFLDTGYHFEETIGTRDAVDAVMDVNVITLTPRQTVAEQDAEYGPKLHDRDPDLCCALRKVKPLEEGLTAYDAWATGLRRDESPTRANTPVVGWDEKRQKVKISPIARWTQDDVDAYVAEHGVLTNPLLMDGYASVGCAPCTRRVAEGEDARSGRWAGRGKTECGLHG
>NZ_CP019798.1|WP_030856051.1|6415152_6415698_-|adenylyl-sulfate-kinase
MSVSDQGATVWLTGLPSAGKTTIAYALAERLRAEGHRVEVLDGDEIREFLSAGLGFSREDRHTNVQRIGFVAELLASNGVKALVPVIAPFADSREAVRTRHAAAATDYLEVHVATPVEVCSERDVKGLYAKQAAGEISGLTGVDDPYEAPESPDLRIESHTQTVQESASALHALLTERGLA
>NZ_CP019798.1|WP_030856049.1|6414217_6415156_-|sulfate-adenylyltransferase-subunit-CysD
MTTTVAHVHEETDAPYALSHLDALESEAVHIFREVAGEFEKPVILFSGGKDSIVMLHLALKAFAPAPVPFALLHVDTGHNFPEVLEYRDRTVAEHGLRLHVASVQDYIDAGKLRERPDGTRNPLQTVPLTEAIQSLKFDAVFGGGRRDEEKARAKERVFSLRDEFSQWDPRRQRPELWQLYNGRHAPGEHVRVFPLSNWTELDVWQYIAREGIELPEIYFAHEREVFKRNGMWLTAGEWGGPKQDETPERRLVRYRTVGDMSCTGAVDSDAVTLDAVIAEIAVSRLTERGATRADDKMSEAAMEDRKREGYF
>NZ_CP019798.1|WP_060180888.1|6412865_6414215_-|50S-ribosome-binding-GTPase
MTSTTDQVGGLDDLAATTLLRFATAGSVDDGKSTLVGRLLHDSKSVLTDQMEAVEAVSAQRGQEAPDLALLTDGLRAEREQGITIDVAYRYFATARRRFILADTPGHVQYTRNMVTGASTADLAVVLVDARNGVIEQTRRHAAVAALLRVPHVVLAVNKMDLVGYQESVFAAIAEEFTAYASDLGVPEITAIPISALAGDNVVEPSANMDWYGGPTVLEHLETVPVSHDLTACPARFPVQYVIRPQSAEHPDYRGYAGQIASGVLRVGEAVTVLPSGRTSVIEGIDALGESVDIAWAPQSVTVRLKDDIDISRGDLIAPSAKAPATTQDVVATVCHVADQPLSVGARVLLKHTTRTVKAIVKEIPSRLTLDDLSQHPEPGQLVANDIGLVVVRTAEPLALDAYADSRRTGSFLLIDPADGTTLAAGMAGESFASQAETAVQPDDEGWDF
>NZ_CP019798.1|WP_078095367.1|6411546_6412674_-|ABC-transporter-substrate-binding-protein
MPDTGTLRTSLRRGLAAAASLPLLIGALASCGYGSQAQDAAGEKANASAAGGKRLSASEVRIGYFPNLTHATALVGLQEGLIQQELGGTRIRPQSFNAGPSEIEALNGGSLDIGFIGASPSINGYVKSKGSNLRIISGSASGGVKLVVNPEKIKTLDDLKGKKIATPQKGNTQDVAFLNWISEKGWTVDPESGKGDVSVVRTDNKVTPDAFKQGSIDGAWVPEPTASKLVSDGGSVLLDETTLWPEKKFVITNIIVSQKFLKEHPDVVEAVLKGTVKTNEWINANPDQAKASANARLAAEGGKPLDAKVIDPAWQSILVTDDPLAATLKAQADHAVKAELIQQPDLAGIYDLTLLNKVLKAAGKPEVSDAGLGAK
>NZ_CP019798.1|WP_078095366.1|6410717_6411512_-|ABC-transporter-ATP-binding-protein
MATTLAKAAEGTVAEHRHAARIEHVSKSFSGPAGSQLVLDDISLDVAPGEFVTILGASGCGKSTLLNLVAGLDRPTAGSIATPGGRPALMFQEHALFPWLTAGKNIELALRLRGIAKSDRRTEAERLLELVRLGGAHGKRVHELSGGMRQRVALARALAQDSRLLLMDEPFAALDAITRDVLHGELTRIWAETGLSVLFVTHNVREAVRLAQRVVLLSSRPGRVAKEWTVDIPQPRRIEDADVAELSLEITEHLRGEIRRHGQH
>NZ_CP019798.1|WP_078095365.1|6409846_6410731_-|ABC-transporter-permease
MASTETKATTDDLAGLEAGLDALDAVQTHRTPVREVLVKKVLPPFLAVGLVLAIWQVLVSLKVTDETKLPALSAVWDSLSDMWLKGTLLEVIWTSVSRGLLGFLLALAIGTPLGLLVARVKFVRAAIGPILQGLQSLPSVAWVPPAVLWFGLNDAMMFTVILLGAVPSIANGLVSGIDQVPPLFLRAGRTLGATGLRGAWHVVMPAALPGYVAGLKQGWAFSWRSLMAAEIIASSPDLGLGLGQLLENGRNNIDLPGVFLAIILILVVGIAIDLLIFSPIERYVLRSRGLLVKS
>NZ_CP019798.1|WP_030856062.1|6419362_6419926_-|GNAT-family-N-acetyltransferase
MSTITLTTWSLEMTSPADLVPAAPAGPEISVVRSEVPSPEFSRFLYASVGGDIHWTDRLSLTRAQWVEQLDRPGVETWVAYDRGTPAGYVELDPQDDGVVEIMYFGLLPDFRGRRIGGHLLTVGVERAWDLASRWPQREATRRVWVHTCSQDGPTAMANYQRRGFKVFKTETEQKEETPTPGPWPGA
>NZ_CP019798.1|WP_051700853.1|6419931_6421194_-|GAF-domain-containing-protein
MHPREATRLLKGVRAAALAGDRPPAAPRPEIAESWRRMLAGGVHPDRDARSRMLSAAETEERRHVSPLREVLPVLREGLLPALDGALHIMVVADADGRLLWREGHSSILRKADRLGFAVGADWDEAVVGTNGVGTALVARRPVQVFSAEHFVSSHHDWTCAGAPVRDPRDGRLLGVVDVSGPLATMHPATLAWVGSVARLAERELRIRHLESLERLRTVAAPLLARLPGRALAVDPHGWTAAVTGLAPADRIPLPKDFAPGRVWVPQLGDCVAEPLPGGWLLRIAQDRAGTAATRVVLDVSRAGSWSATVYGSSGSWSQELSPRHAELLFLLAESPRGRSAAELAAEVFGDPTRTVTVRAELSRVRRHLAGVLAHRPYRFAEDVEVELIRPEDPAALLPHSTAPAVVRARLGRTGPGMIP
>NZ_CP019798.1|WP_078095368.1|6421562_6423206_-|acyl-CoA-dehydrogenase-family-protein
MAATTHTVSNQAPPLVGHDVYNGDRALAEGVERHLASADPELLGEVREELTDLGRAAGSAQAQEWGAQANDNPPKLRTHDRYGHRIDEVEFHPAWHRLLGQAVGAGLTDAWGRPAGHLRRAAGFFLWSQAEAGHGCPVSMTHAAVPALRADPAIAAEWEPRLTSHVYEEGLRPAAQKAGVLFGMGMTEKQGGSDVRANTTAAVPLDASGEYLLTGHKWFCSAPMCDGFLVLAQAPGGLTCFLVPRVLEDGTRNVFAIQRLKDKLGNKSNASSEVEFDGTWARRVGEEGRGVRTIIEMVAATRLDCVIGSAALMRQALTQAVHHAEHRSAFGALLIDQPLMRNVLADLALESEAATTLTLRLAAANDAGTEQEKAFLRLAVPAAKYWVTKRCTPMVAEALECLGGNGYVEESGLPRLLRESPLNSIWEGSGNVQALDVLRALQREPQALNAFLQEVGLARGADHRLDSAIKDLLTDLADLAGIEARARRVVERMALVLQGSLLVRWAPPEVADAFCASRLGGDWGAAFGTLPHSLDLRAVVERARITG
>NZ_CP019798.1|WP_030856072.1|6423223_6424339_+|YihY/virulence-factor-BrkB-family-protein
MQPAKETPERIPGRLHRARALYRNVSKRKMGWLLLKDTVNSCIEYRILGLAAEAAFFTLLSLPPLFLGLLGLLGYVDGWTDTRTVESIEENILRAVGTVLSDRGVNDIARPLLDDVTRSGRPDLISLGFAFALWSGSRAVNVFIDTITVMYGLDGHRGIVKTRLLAFLLYVIALLIGAIVLPLMVVGPDAVVRLVPWGTEVIAVLYWPTVTLLSIAFLTTLYHVSVPVRSPWIEDVPGALVALAMWVLGSFLLRIYLTNTVEGPTIYGSLAAPVAVLLWIGISAFAVLVGAAVNAAIDRVWPSVATAAAREANERIREAEAAQLVARAAAWRAMAEGESEDDEDEGMPSEFPERWSKFLPPEDYSSRLRKH
>NZ_CP019798.1|WP_078095369.1|6424538_6425012_+|GNAT-family-N-acetyltransferase
MLDSAVAWMNARGNTEQWGTIPYSQRPGGTERVERYTTENTPYVAELAGVPVGALVLDSGPSPQLPIAPAGEPERYVRLLVSDRRYAGRGIGAALLAHAAEETRRAGIALLRVDCWAGGGGELVAFYVRSGFTPTEPFLSGDWPGQVLARRLDGAPG
>NZ_CP019798.1|WP_159425595.1|6425267_6427700_-|VCBS-repeat-containing-protein
MLAVVAALLISIGAALPTARAADRPVTFCGSVINVINCRWGTDRAAYNIVGNAYSFFNGSTVRVEGGNLYLGNAGIYRNNTFVADRIIIHENAVEGLTAPGNGNVFIGNVEIARVNQIYREVVELRECTTNLVRTTTTGWNFEEFDEAGDARPDGLLGPADLQAVLNDDDFTDAARDCARLLSRFDYEHFSAVQTERGAQDNRMANRDDFQRFNDHLARCEEEMERQAVAGDAGGMVTALLDCARDGNENGPANTGSDGAGGNATQPDPDPGTDGQFPGQNTQPGDWTIGSGLGVGAVKDELKKRGLPQLPTTASTTDIRMLPLGDSITYGVGAQGGSSYRGRLWDFLAHDLRSLDFAGTVKSGTGPDRDHEGHKGWSIGQIDAIANCTMARYRPNVVTLHIGTNDMNGNVDVDQAPARLRTLITKIVSAAPETTVLVATLVPSSTPEVNERIKRYNAAIPGIVNSFRAAGDHVRLVDMNALTPEDLNDWLHPKALGYEKMANAFYRGIHQAMSDGWIARPRPQDPSPCATQRPATDDGWDWKGTVASGVGAPRSDLRWADLNGDGRDDYLVIDGQGRIRAWLNDGPAPGSGWKWTWTGEVASGVGATRDQVRLADLNGDNRVDYLVVDDQGKARAWMNSGPAAGGGWAWKWTGEVASGVGAASDQVRFADLNGDKRADYLVVDGQGRARAWLNNGPADGGGWAWGWKGEVASGVGATRDQVRLVDLDGDDRVDYLVLGDHGQVRAWMNSGPAAGGGWAWKWTGEVASGVGAPADNIDFADLDGDRRSDYLVVRDNGAATGWLNDRLPLG
>NZ_CP019798.1|WP_030853776.1|6428236_6429403_+|ribosome-small-subunit-dependent-GTPase-A
MSDASLHPFSSSAVQHPLAVYGWDEGWEAEFTPYAAQGLVPGRVVRVDRGQCDVATPDGVVRADTAFVVPHDPMKVVCTGDWVAVDPEGSDPRYAQTILPRRTAFVRSTSSKRSEGQVLATNIDHIVICVSLAVELDLGRIERFLALAMASSSGDALLRTSADSWASGAQPLVVLTKADLVPDPVTLGHLVQDVETTAPGVQVLTASSHTGEGTDVLGAIVASGTSVLLGVSGAGKSTLANALLGTDAMEVQAIRDVDGKGRHTTTTRNLLVLPGGGVLIDTPGLRGVGLFDAEAGVGQVFSEIEDYAAECRFHDCAHEAEPGCAVLAALESGALPERRLESYRKLLRENQRIVAKTDARLRSEIRRDWRLKSAEGRANYSAKRGGRV
>NZ_CP019798.1|WP_078095371.1|6429570_6431217_+|hypothetical-protein
MRTRRLIVSAAVIAAGAGLVPGTAQADEPGKAEAHGVSAPDAALGKAAASNFDTFTSAAERTVRPAGKGKAQGAAATEPTVGLTAKGTSARGISLGLAVGIDPDAQISAYIEWGDGSTDVFDTYGPTDRTVAHSYAEIGAYTIKVTLKDATGDRGTNTLAVVTPGSDFTPYAPTRLLDTRNGTGGPKAKVPAYGTTRVQISGNGNIPTGVTAVVLNVTATNTTSGGHVTVWPAGSERPITSNVNFTKGQTVPNLVIVPVDRNGFVNLYNGGWESVDLIADVTGYFTRTSSSGYTALNPTRFVDTRNGTGTAQGQVRGQSTFNVRFTGRDGIPFGTTAVALNVTVTNPREDGHLTVFPGGSTAPSTSNVNFRAGQTVANSVIVPVGPDGTVNFRNGAWSGTDVIVDVVGYYHPASWGAYLPFVPERLLDTRDSSDWAWGPLEGQGYIYMPLSTQYPSNTAYVLNTTVTNTRGEGYLTVSPDPNSLSAYKGGWASWPTPPNSSNLNWKRNDTVPNLVQAGMGSNGIVDFWNRGWDDIDLVVDIFGVYQTN
>NZ_CP019798.1|WP_078095372.1|6431348_6431966_-|GNAT-family-N-acetyltransferase
MTRMPMTNAPKTATVDDARMVGRTLAAAFDDDPMMRWFFPDGASREAGLNRYFTTLFTRQYVHHGVCERTDAAASFWVAPEGQAKAVPDEETVRELQDILGDRAALFREAVESAAEHAPTEPHWYLAVVGADPAARGRGHGAALLRSGLAQADAAGLPVYLESSKPDNLPFYEHFGFTVLGEARLPGGGPVLWAMRRAPRPAADA
>NZ_CP019798.1|WP_078095373.1|6432092_6432575_-|DUF456-domain-containing-protein
MDVPQLLLVGLVLLFGLVGVLVPGVPGTWLVWAGLLWWSLLERSALSWSLLVAATALLLVVQAVKWQLPARRPHEVPATPRTAVFAGAGALLGFVLVPVVGAVPGFVGGVYLCERLRLGGHGEAWASTRAVMRAVGTSVLVELFGCLLVVGAWVGAVAAG

Crispr_ID: NZ_CP019798_13

• CRISPR_ID: NZ_CP019798_13
• CRISPR_location: 6637823-6637931
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP019798_13

Consensus_repeat	Method
CGGGCGCGGGGGCCTGGCGCGCGTC	CRISPRCasFinder

spacers of NZ_CP019798_13

>13.1|6637848|59|NZ_CP019798|CRISPRCasFinder
AGCGCCGGGAGACGTTGCGCCCGCGATGCCGCACGCCCGGCCGCAGGTCCCGGACGGTG

CRISPR arrays and Neighbor proteins around NZ_CP019798_13

CRISPR arrays

The CRISPR arrays of NZ_CP019798_13

>merge|NZ_CP019798|13|6637823-6637931|CRISPRCasFinder
CGGGCGCGGGGGCCTGGCGCGCGTCAGCGCCGGGAGACGTTGCGCCCGCGATGCCGCACGCCCGGCCGCAGGTCCCGGACGGTGCGGGCGCGGGGGTCTGGCGCGCGTC

>NZ_CP019798|13|9|6637823-6637931|CRISPRCasFinder
CGGGCGCGGGGGCCTGGCGCGCGTC	AGCGCCGGGAGACGTTGCGCCCGCGATGCCGCACGCCCGGCCGCAGGTCCCGGACGGTG
CGGGCGCGGGGGTCTGGCGCGCGTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019798.1|WP_078095449.1|6630345_6632151_+|gamma-glutamyltransferase	unknown	unknown	gnl|CDD|223482
NZ_CP019798.1|WP_030855090.1|6646326_6646845_+|O-acetyl-ADP-ribose-deacetylase	unknown	unknown	gnl|CDD|234759
NZ_CP019798.1|WP_030855114.1|6639061_6639904_+|acyltransferase	unknown	unknown	gnl|CDD|143592
NZ_CP019798.1|WP_158076127.1|6633398_6633575_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078095455.1|6644805_6646224_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224154
NZ_CP019798.1|WP_078095456.1|6648490_6649705_+|aspartate/tyrosine/aromatic-aminotransferase	unknown	unknown	gnl|CDD|181731
NZ_CP019798.1|WP_030855096.1|6643906_6644731_+|inositol-monophosphatase	unknown	unknown	gnl|CDD|238775
NZ_CP019798.1|WP_078095450.1|6632167_6632935_-|type-I-methionyl-aminopeptidase	unknown	unknown	gnl|CDD|238519
NZ_CP019798.1|WP_030855109.1|6641208_6642609_+|dihydropyrimidinase	unknown	unknown	gnl|CDD|236240
NZ_CP019798.1|WP_078096385.1|6635616_6636555_-|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133378
NZ_CP019798.1|WP_078095454.1|6642630_6643632_+|TIGR03842-family-LLM-class-F420-dependent-oxidoreductase	unknown	unknown	gnl|CDD|163554
NZ_CP019798.1|WP_030855121.1|6632999_6633251_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|376540
NZ_CP019798.1|WP_078095451.1|6634614_6635529_-|IS982-family-transposase	unknown	unknown	gnl|CDD|376573
NZ_CP019798.1|WP_078095448.1|6628199_6629459_+|cytochrome-P450	unknown	unknown	gnl|CDD|225035
NZ_CP019798.1|WP_060177710.1|6633888_6634551_+|fasciclin-domain-containing-protein	unknown	unknown	gnl|CDD|367095
NZ_CP019798.1|WP_037834552.1|6646901_6647384_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP019798.1|WP_060177790.1|6647622_6648498_+|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP019798.1|WP_030855118.1|6636789_6637170_+|PPOX-class-F420-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274712
NZ_CP019798.1|WP_030855131.1|6629418_6630144_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP019798.1|WP_078095453.1|6639900_6641196_+|aspartate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|99735

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP019798.1|WP_078095449.1|6630345_6632151_+|gamma-glutamyltransferase	gnl|CDD|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP019798.1|WP_030855090.1|6646326_6646845_+|O-acetyl-ADP-ribose-deacetylase	gnl|CDD|234759	PRK00431, PRK00431, ADP-ribose-binding protein.	9.35446e-86
NZ_CP019798.1|WP_030855114.1|6639061_6639904_+|acyltransferase	gnl|CDD|143592	cd07568, ML_beta-AS_like, mammalian-like beta-alanine synthase (beta-AS) and similar proteins (class 5 nitrilases). This family includes mammalian-like beta-AS (EC 3.5.1.6, also known as beta-ureidopropionase or N-carbamoyl-beta-alanine amidohydrolase). This enzyme catalyzes the third and final step in the catabolic pyrimidine catabolic pathway responsible for the degradation of uracil and thymine, the hydrolysis of N-carbamyl-beta-alanine and N-carbamyl-beta-aminoisobutyrate to the beta-amino acids, beta-alanine and beta-aminoisobutyrate respectively. This family belongs to a larger nitrilase superfamily comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), this subgroup corresponds to class 5. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer. Beta-ASs from this subgroup are found in various oligomeric states, dimer (human), hexamer (calf liver), decamer (Arabidopsis and Zea mays), and in the case of Drosophila melanogaster beta-AS, as a homooctamer assembled as a left-handed helical turn, with the possibility of higher order oligomers formed by adding dimers at either end. Rat beta-AS changes its oligomeric state (hexamer, trimer, dodecamer) in response to allosteric effectors. Eukaryotic Saccharomyces kluyveri beta-AS belongs to a different superfamily.	3.92316e-152
NZ_CP019798.1|WP_078095453.1|6639900_6641196_+|aspartate-aminotransferase-family-protein	gnl|CDD|99735	cd00610, OAT_like, Acetyl ornithine aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The major groups in this CD correspond to ornithine aminotransferase, acetylornithine aminotransferase, alanine-glyoxylate aminotransferase, dialkylglycine decarboxylase, 4-aminobutyrate aminotransferase, beta-alanine-pyruvate aminotransferase, adenosylmethionine-8-amino-7-oxononanoate aminotransferase, and glutamate-1-semialdehyde 2,1-aminomutase. All the enzymes belonging to this family act on basic amino acids and their derivatives are involved in transamination or decarboxylation.	6.65331e-137
NZ_CP019798.1|WP_078095455.1|6644805_6646224_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224154	COG1233, COG1233, Phytoene dehydrogenase and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	1.20145e-85
NZ_CP019798.1|WP_078095456.1|6648490_6649705_+|aspartate/tyrosine/aromatic-aminotransferase	gnl|CDD|181731	PRK09257, PRK09257, aromatic amino acid transaminase.	0
NZ_CP019798.1|WP_078095450.1|6632167_6632935_-|type-I-methionyl-aminopeptidase	gnl|CDD|238519	cd01086, MetAP1, Methionine Aminopeptidase 1. E.C. 3.4.11.18. Also known as methionyl aminopeptidase and Peptidase M. Catalyzes release of N-terminal amino acids, preferentially methionine, from peptides and arylamides.	5.0141e-117
NZ_CP019798.1|WP_030855109.1|6641208_6642609_+|dihydropyrimidinase	gnl|CDD|236240	PRK08323, PRK08323, phenylhydantoinase; Validated.	0
NZ_CP019798.1|WP_078096385.1|6635616_6636555_-|MerR-family-transcriptional-regulator	gnl|CDD|133378	cd00592, HTH_MerR-like, Helix-Turn-Helix DNA binding domain of MerR-like transcription regulators. Helix-turn-helix (HTH) MerR-like transcription regulator, N-terminal domain. The MerR family transcription regulators have been shown to mediate responses to stress including exposure to heavy metals, drugs, or oxygen radicals in eubacterial and some archaeal species. They regulate transcription of multidrug/metal ion transporter genes and oxidative stress regulons by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	1.13717e-22
NZ_CP019798.1|WP_078095454.1|6642630_6643632_+|TIGR03842-family-LLM-class-F420-dependent-oxidoreductase	gnl|CDD|163554	TIGR03842, F420_CPS_4043, F420-dependent oxidoreductase, CPS_4043 family. This model represents a family of putative F420-dependent oxidoreductases, fairly closely related to 5,10-methylenetetrahydromethanopterin reductase (mer, TIGR03555), both within the bacterial luciferase-like monoxygenase (LLM) family. A fairly deep split (to about 40 % sequence identity) in the present family separates a strictly Actinobacterial clade from an alpha/beta/gamma-proteobacterial clade, in which the member is often the only apparent F420-dependent LLM family member. The specific function, and whether Actinobacterial and Proteobacterial clades differ in function, are unknown. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP019798.1|WP_030855121.1|6632999_6633251_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|376540	pfam01381, HTH_3, Helix-turn-helix. This large family of DNA binding helix-turn helix proteins includes Cro and CI. Within Neisseria gonorrhoeae NGO_0477, the full protein fold incorporates a helix-turn-helix motif, but the function of this member is unlikely to be that of a DNA-binding regulator, the function of most other members, so is not necessarily characteristic of the whole family.	6.63302e-07
NZ_CP019798.1|WP_078095451.1|6634614_6635529_-|IS982-family-transposase	gnl|CDD|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	9.05891e-10
NZ_CP019798.1|WP_078095448.1|6628199_6629459_+|cytochrome-P450	gnl|CDD|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	1.86145e-75
NZ_CP019798.1|WP_060177710.1|6633888_6634551_+|fasciclin-domain-containing-protein	gnl|CDD|367095	pfam02469, Fasciclin, Fasciclin domain. This extracellular domain is found repeated four times in grasshopper fasciclin I as well as in proteins from mammals, sea urchins, plants, yeast and bacteria.	1.86208e-35
NZ_CP019798.1|WP_037834552.1|6646901_6647384_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	1.7652e-45
NZ_CP019798.1|WP_060177790.1|6647622_6648498_+|DMT-family-transporter	gnl|CDD|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	2.98441e-07
NZ_CP019798.1|WP_030855118.1|6636789_6637170_+|PPOX-class-F420-dependent-oxidoreductase	gnl|CDD|274712	TIGR03666, Rv2061_F420, PPOX class probable F420-dependent enzyme, Rv2061 family. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomycetales, make F420. A variant of the Partial Phylogenetic Profiling algorithm, SIMBAL, shows that this protein likely binds F420 in a cleft similar to that in which the homologous enzyme pyridoxamine phosphate oxidase (PPOX) binds FMN. [Unknown function, Enzymes of unknown specificity].	1.81044e-43
NZ_CP019798.1|WP_030855096.1|6643906_6644731_+|inositol-monophosphatase	gnl|CDD|238775	cd01517, PAP_phosphatase, PAP-phosphatase_like domains. PAP-phosphatase is a member of the inositol monophosphatase family, and catalyses the hydrolysis of 3'-phosphoadenosine-5'-phosphate (PAP) to AMP. In Saccharomyces cerevisiae, HAL2 (MET22) is involved in methionine biosynthesis and provides increased salt tolerance when over-expressed. Bacterial members of this domain family may differ in their substrate specificity and dephosphorylate different targets, as the substrate binding site does not appear to be conserved in that sub-set.	8.06581e-55

Protein sequences

>NZ_CP019798.1|WP_030855118.1|6636789_6637170_+|PPOX-class-F420-dependent-oxidoreductase
MGLQELGSARYVSLTTFRKDGTPVATPVWAVADGGELYVWTRSDSWKVKRIRNDGRVTVAACDVRGRLEEGATVVEGQARLLDEEGLRRVRKLMSRKYTWQFWAVDVPAALVRRGKRPHTAIAVKL
>NZ_CP019798.1|WP_078096385.1|6635616_6636555_-|MerR-family-transcriptional-regulator
MDVTTLYSIGELSRRTGLSVRTIRFYSDSGVVAPTTRSPAGYRLYDLDALLRLELLRTLRELGMNLPTIQRVLDRELSVAEVAAAHADAMDVQIRMLQLRRSVLRVVASRGSNPEETKLMHRLTQLSGEERRRLIDDFMDGTFGTVDADPAAVAMVRAATPDLPDDPTGEQVAAWVELAELVGDEDFRARMRRTAVRQAAGRPLDIERDAGEDLMEFTRQKVAEARKSGIDPLCNRAAPVIDDLVHRFSEVFARTPDTEFRHWMAEQFEEAHDPMVDRYWQLVWIVNGWQVVPNLIPVYPWLTQALRNDRAA
>NZ_CP019798.1|WP_078095451.1|6634614_6635529_-|IS982-family-transposase
MTNDLDTLTTALYARIDDELKASPWLAPWRPAVGITPRLSDAELITLAVMSALLGYTSERRWLRRVGRDFGHLFPYVPQQSGYNKRVRAAFPLLTSMIRIVARDTSLWSDDVWLVDSTPVGCGCSRETAKRSDLAGWAQYGYCASHSRYFWGLRLHLVCTLGGLPVLFALTGAKADERETLRDMLDTAPDVLATHPGQTIIGDKNYFGREFEHGLAERHLKLLRPARKGEAKLAGSHLFKPLRQVIESINQTFKGQLNLERHGGKSPAGVSARVLCRILALTAAIWHNDQTGQPVKRSLTAYDH
>NZ_CP019798.1|WP_060177710.1|6633888_6634551_+|fasciclin-domain-containing-protein
MNNTRTATRIRRTAIAVAAAAVLPFSLAACSDSGGDAGAAPAAGSAQDRAADTPAAADGAVTAEGPFGPACAGVPKQGAGSFEGMAKDPVATAASNNPALSTLVAAVKKAGLVDTLNNAKDITVFAPTDDAFAKIPKADLDKVLADKATLTKILTYHVVGQKLTPRQLESGTFETLQKGELTTDGLGEEYKVNGTSNVVCGEVETANATVYLVDTVLMPK
>NZ_CP019798.1|WP_158076127.1|6633398_6633575_+|hypothetical-protein
MSATNAAERLGCAAVGALLAGGLLLAACALPDDRPGPVREADGRERTGAVEPGGPYGR
>NZ_CP019798.1|WP_030855121.1|6632999_6633251_+|helix-turn-helix-transcriptional-regulator
MVRTPLTPEERERGERLGALLREARGTRSMVEVAAGAGLSAETLRKIETGRAPTPAFFTVAALAEALGLSLDDVLRRCAAVPA
>NZ_CP019798.1|WP_078095450.1|6632167_6632935_-|type-I-methionyl-aminopeptidase
MVELKTAPEIEKMRAAGRVVARALAAVRKAAHVGVALSDLDRVAREVLRGAGATSPFLGYRPSFAPVPFPAVVCASVNDAIVHGIPDGYRLSDGDLVSIDCGAKLGGWAGDAAVSFTVGRARPEDLRLIGTSEAALAAGIAAAVPGNRIGDIAHAVGTACRSAGYGVPDGFGGHGIGRSMHEDPGVPNEGPPGRGMKLRPGMVLAIEPMLIAGGTDDYRCDGDGWTLRTVDGSRAAHSEHTVAITARGPRILTAP
>NZ_CP019798.1|WP_078095449.1|6630345_6632151_+|gamma-glutamyltransferase
MHRPAVARTLPMLTVVAALVGAGAAPPSAAAPAPPAKVPVAAGHGGAVASVDADASAAGIAVLRSGGNAVDAAVATAAALGVTEPYSAGIGGGGYFVYYDARARRVHTIDGRETAPATATAALFQENGQPIPFAEGQTSGLGVGVPGTPATWKSALDAWGSRPLRQLLRPAEKLARDGFTVDATFRAQTELNEARFRDFPDTSKLFLPGGSLPVVGSTFKNPDLADTYAELARKGTGALYRGPIADDIVRTVRTPPVDPAATRRVRPGDLTAGDLRAYGTKRQEPTRVGYRGLDVYSMAPSSSGGTTVGEALNILERTDLSKLSGAQYLHRFIEASRISFADRGRWVGDPAAVDVPTRQLLSQRFADSRACLIDPDRALTSPLAPGDPRHPQPCATTGQAAPTTYEGENTTHLTVADRWGNVVSYTLTIESTGGSAITVPGRGFLLNNELTDFSFAPAAPGVPDPNLPGPGKRPRSSMSPTIVLDDGRPVLAVGSPGGATIITTVLQTLTGHLDRGLPLVDAIAAPRASQRNQTTTELEPGLWNSPLRAELEALGHGFRQNPEIGAATAVQRLPDGRWLAAAETSRRGGGSAMVVRPHGTP
>NZ_CP019798.1|WP_030855131.1|6629418_6630144_-|hypothetical-protein
MDDDVRNIVLGVIATAVSGGFGWFSRTYLWRRALRRKQAFFGLPTGADCLFVVNRQMGGKESSLHRNDAFALLEISALIKDCGANVQVVTHDTARQGFGDRAEFCVGGPTSNARTTAHLASMLPGITVNTDSEQHENRGAIQVGGETYRWRNGLEEYVLLARLTGGEGGRPVFLLSGQTAVSNQAAARYLNRQHTQLARKYGADSFCLVLKVVNSDAYGPDVTELVADVTRAARTPAAAAV
>NZ_CP019798.1|WP_078095448.1|6628199_6629459_+|cytochrome-P450
MDHAADVPDVFDPRIYAAGVPHERYRLLRDRHPVAWQPEPEIAPWPAGPGFWAVTRHADVVRVLRDHGTYSSWLGATQIRDPDPADLPFLRRTMLNQDPPEHGRLRRLVARAFTPARVDAFAGRVRERARTLLAAARDAAEDGAADLVGTVTDEYALLNLTDLLGVPPADRALLLEWTVRVIGYQDPDDAPAPLLGPDGTPLNPRSPALLGEMFAYARALAAHKRDHPGDDVMTALATAGLDPAELEMFFFLLTVAGNDTVRSAAPGGLLALAHAPDEHRRLAEGKATAQSAVEELLRVHPPVLSFRRTATVDHELAGQPVRAGDKVVVFHASANHDERVFADPGRLDLGRTPNPHVSFGDGPHVCLGAHFARLQLRTLYEEWCAAMPPPELAGPPKRLVSNFINGITRLPLRVSGPPG
>NZ_CP019798.1|WP_030855114.1|6639061_6639904_+|acyltransferase
MAQVVRAALVQATWTGDTESMIAKHEDHARRAAAEGAKIIGFQEVFNAPYFCQVQEPEHYRWAEAVPDGPTVRRMQDLARETGMVVVVPVFELESEGFYYNTAAVIDADGTYLGKYRKHHIPQVKGFWEKYYFRPGNLGWPVFDTAVGRVGVYICYDRHFPEGWRQLGLAGAQLVYNPSATHRGLSAHLWQLEQPAAAVANEYFVAAINRIGQEEYGDNDFYGTSYFVDPRGQFVGDVASDKEEELLVRDLDFDLIKEVRDQWAFYRDRRPDAYGGLVQP
>NZ_CP019798.1|WP_078095453.1|6639900_6641196_+|aspartate-aminotransferase-family-protein
MTNPTPLHNRHRTVLPDWLALYYKNPIELTHGEGRHVWDADGNRYLDFFGGILTTMTAHALPEVTKAVSEQAGRIIHSSTLYLNRPMIELAERIAALSGIPDARVFFTTSGTEANDTALLLATTYRRSNQILAMRNSYHGRSFSTVSITGNRGWSPTSLSPLQTYYVHGAVRTRGPFAHLDDTAFTAAAVADLDDVLGQARGGVAALIAEPIQGVGGFTSPPDGLYGAFREVLDRHGILWISDEVQTGWGRTGDHFWGWQAHAQNGPPDILTFAKGIGNGMSIGGVVARAEVMNCLDSQSISTFGGSPVTMAAGVANLGYLLEHDLQGNARRVGGLLLERLRGIAAAVPAVREVRGRGLMAGIELTRPGTDEADPDAASAVLEAAREGGLLLGKGGGHNTSVLRIAPPLSLTVAEAEEGAEILEQALRSVE
>NZ_CP019798.1|WP_030855109.1|6641208_6642609_+|dihydropyrimidinase
MSNRTLITGGLVVTAADELHADVLIEDGRVAALAAHGSAAAGAWTAERTIDATGKYVIPGGVDAHTHMELPFGGTSASDTFETGTRAAAWGGTTTIVDFAVQSVGHSLREGLDTWYAKADGNCAVDYAFHMILSDVNEGTLKEMDLLVGEGVTSFKLFMAYPGVFYSDDGQILRAMQRGASNGGLIMMHAENGIAIDVLVEQALARGETDPRHHGEVRKVLLEAEATHRAIQLARVAGSPLYVVHVSAEEAVAELAAARDKGLPVFGETCPQYLFLSTDNLAEPDFQGAKYVCSTPLRPREHQAALWRGLRTNDLQVVSTDHCPFCFRGQKELGRGDFSKIPNGLPGVENRMDLLHQAVVDGHISRRRWIEIACATPARMFGLYPKKGTIAPGADADIVLYDPHAEQVISAETHHMNVDYSAYEGKRITGRVDTVLSRGELVVDRREYTGRAGHGAFVHRSTCQYL
>NZ_CP019798.1|WP_078095454.1|6642630_6643632_+|TIGR03842-family-LLM-class-F420-dependent-oxidoreductase
MDFGLVLQTDPPASQVISLMKRAERNGFRYGWTFDSAVLWQEPFVIYSQILANTQKLHVGPMVTNPGTRTWEVTASTFATLNDMYGNRTVCGIGRGDSAMRVAGRAPNTLARLGEAMDVIRDLAEGREASVDGNPIRIPWIKDGRLPVWMAAYGPKALALAGQKADGFILQLADPFLTEWMIKAVRQAAAEAGRDPSAITICVAAPAYVGEDLAHARDQCRWFGGMVGNHVADLVSRYGEHSGMVPEELTEYIKARQGYDYSHHGRAGNPSTDFVPDEIVDRFCLLGPAQAHIEKLRALRDLGVDQFAVYDMHDAKESTIDAYGTQIIPALNT
>NZ_CP019798.1|WP_030855096.1|6643906_6644731_+|inositol-monophosphatase
MIDEFLAQGLPDVEEAVRKAAAVEIMPRFRQLAEHEVVEKSGPHDLVTVADRRAEEHLTASLTRLLPGSVVVGEEAVHADPTVYEALRADAPVWIVDPVDGTRQFVGGDPAFCTLVALAQRGEILASWTFAPALEELATAVRGQGAYVNGQVIHSGSPEPGADLRVAIAHPLYTTDENKRTLARLDVPGVAARPCGSAGLEYLKVARGEVDALAFTWPSAWDHAAGLLLVAEAGGAQSTVDGVPFRVDRDNALPFAVGRDEATVVRVRELLRGR
>NZ_CP019798.1|WP_078095455.1|6644805_6646224_+|NAD(P)/FAD-dependent-oxidoreductase
MPSIFDVVVVGAGPNGLTAAVELARRGFSVAVFEAADTVGGGARTEELTLPGFRHDPCSAVHPLGAGSPVFATMPLKRYGLEWLHAPLPMAHPFDDGTAAVLSRSVAETAASFGPRDAGAYRRLVRPFLGRWDTLARDFMSLPNTALPRDPLTLARFGLAGLPPSTWLLRRFQDERARALFAGLVAHVIAPLGGIGTGAVGLVFALAAHAGGWPMARGGSQSVSDALASYLRDLGGSIHTDFEVKRLDDLPPARAYVFDTSPTALARIARLGRVYDSYRYGASVFKIDYALDGPVPWTAEEPRRAGTVQIGPRTRDIDAALQLASGGRRPRTPFLITAQPSLADPGRAPEGKHVFWAYGHVPAGWDGDLTEAVERQLERFAPGFRDLVLARATAGPPQLAARNPNYVGGDIACGAASGLQLLLRPRLSLSPYTTAHPAVFLCSSATPPGPGVHGMSGHNAAKAVWRHLRQAG
>NZ_CP019798.1|WP_030855090.1|6646326_6646845_+|O-acetyl-ADP-ribose-deacetylase
MVRITLVRGDITAERADAIVNAANSSLLGGGGVDGAIHRKGGPEILAACEDLRRGHYGKGLPTGRAVATTAGRLAAEHVIHTVGPVWSREEDRSELLASCYRESLRVADELGARTVAFPAISTGVYGWPMDDGARIAVHTVRAARTEVQEVRFVLFDEAAHAAFEAAVAAAR
>NZ_CP019798.1|WP_037834552.1|6646901_6647384_-|Lrp/AsnC-family-transcriptional-regulator
MDAVDLQIIRELQTDGRLSNQELADRVRLSPSPCLRRVRRLEEAGLIRGYTAMVDQVAYGLPVTVFVRIRLERHTAQAVRLFEEHVAGIEHIQDCYLMAGSSDYLLRVVIEDLEAYEALVRHRIHAIPGIASIESSFAYGSVKQSRTYPKPAPGASRRPR
>NZ_CP019798.1|WP_060177790.1|6647622_6648498_+|DMT-family-transporter
MLALLVTVSIWAAFALSARALSQSSLLPADAALLRFGLPLVVLLPALWRRRRAIAAVRPGPALKIVCGAGVPFFLAAMHGGALTSAAFVGSIVPGMVPLFVSLIMIRRGHGVPRGTQAVGLALIAAGVVALVWRYVVPVDTDVLAGSGILLVASGLWALYTVGLREVDLDPIGSIGLLCLPSFAIVGLLVLTGVLPTGIAHAAGADIALFLVVQGLGVGLCAGLLYAFAIRRLGAERSSVVGSLSPVAVVLLAIPLLGESPTAAVLVGVPLITAGVVLANRRPRPEVPADA
>NZ_CP019798.1|WP_078095456.1|6648490_6649705_+|aspartate/tyrosine/aromatic-aminotransferase
MLELLPTPPTDPLWDLTYEFGGDERPERLNLVLGVYRDQSGTTPVMAAVREAEILLAQRSESKEYRGLSGNAAFNQCLLDLVLGPDGPAERAAAVQTVAGSGALRLLADLVFRTRPGATVWISDPAYVNHRPILEAAGLKVRTYGWRDAAGGFDTAGVLRELADAGRDDVVLLQGCCHNPTGVDPLLDDWEALAESALRGGWVPFVDLAYHGLGDGLEADLLATRMLASRVPEMLIAVSCSKNFGLYSDRVGCAIVLGASARAVRHAETALQNAARTLYSMPPEHGAAVVTAILQDAGLRASWRAELDVMRGRIMANRADLTAHLGNLGCAEQARSLARQKGMFSMLPLTPNQMLRLRRQYAIYGTTSGRINIAGIPAHRIPCLARGIAAVLDTADAPRLRELA

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	374142-374159	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	1228400-1228417	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	3034804-3034821	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	4489283-4489300	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	5582438-5582455	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	7167027-7167044	1	0.944
NZ_CP019798_1	1.3|1068350|18|NZ_CP019798|CRT	1068350-1068367	18	NZ_CP019798.1	7297492-7297509	1	0.944
NZ_CP019798_4	4.4|2096975|45|NZ_CP019798|CRT	2096975-2097019	45	NZ_CP019798.1	2096678-2096722	1	0.978
NZ_CP019798_4	4.9|2097347|48|NZ_CP019798|CRT	2097347-2097394	48	NZ_CP019798.1	2096678-2096725	1	0.979
NZ_CP019798_8	8.1|4720748|26|NZ_CP019798|CRISPRCasFinder	4720748-4720773	26	NZ_CP019798.1	3619510-3619535	1	0.962
NZ_CP019798_3	3.3|2068285|19|NZ_CP019798|CRT	2068285-2068303	19	NZ_CP019798.1	1655429-1655447	2	0.895
NZ_CP019798_3	3.3|2068285|19|NZ_CP019798|CRT	2068285-2068303	19	NZ_CP019798.1	2823866-2823884	2	0.895

1. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 374142-374159, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcgtcggcgatggcttc	Protospacer
*********** ******

2. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 1228400-1228417, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcgtcggcgagggattc	Protospacer
************** ***

3. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 3034804-3034821, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcctcggcgagggcttc	Protospacer
*** **************

4. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 4489283-4489300, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcgtcggcgatggcttc	Protospacer
*********** ******

5. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 5582438-5582455, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcggcggcgagggcttc	Protospacer
**** *************

6. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 7167027-7167044, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggagtcggcgagggcttc	Protospacer
** ***************

7. spacer 1.3|1068350|18|NZ_CP019798|CRT matches to position: 7297492-7297509, mismatch: 1, identity: 0.944

ggcgtcggcgagggcttc	CRISPR spacer
ggcgtcggcgagggcatc	Protospacer
*************** **

8. spacer 4.4|2096975|45|NZ_CP019798|CRT matches to position: 2096678-2096722, mismatch: 1, identity: 0.978

cgccgcggtatcccccacggtcgtcatcacgacgcgggtacgacg	CRISPR spacer
cgccgcggtatccaccacggtcgtcatcacgacgcgggtacgacg	Protospacer
************* *******************************

9. spacer 4.9|2097347|48|NZ_CP019798|CRT matches to position: 2096678-2096725, mismatch: 1, identity: 0.979

cgccgcggtatccaccacggtcgtcatcacgacgcgggtacgagggac	CRISPR spacer
cgccgcggtatccaccacggtcgtcatcacgacgcgggtacgacggac	Protospacer
******************************************* ****

10. spacer 8.1|4720748|26|NZ_CP019798|CRISPRCasFinder matches to position: 3619510-3619535, mismatch: 1, identity: 0.962

tcttgggccggacataggccgccacc	CRISPR spacer
tctggggccggacataggccgccacc	Protospacer
*** **********************

11. spacer 3.3|2068285|19|NZ_CP019798|CRT matches to position: 1655429-1655447, mismatch: 2, identity: 0.895

cacgggcgctaccgcgccc	CRISPR spacer
cacgggcgcgaccgcaccc	Protospacer
********* *****.***

12. spacer 3.3|2068285|19|NZ_CP019798|CRT matches to position: 2823866-2823884, mismatch: 2, identity: 0.895

cacgggcgctaccgcgccc	CRISPR spacer
cacgggcgctccggcgccc	Protospacer
********** * ******

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP019798_1	1.1|1068254|24|NZ_CP019798|CRT	1068254-1068277	24	NC_019959	Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence	35783-35806	2	0.917
NZ_CP019798_1	1.1|1068254|24|NZ_CP019798|CRT	1068254-1068277	24	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	893535-893558	2	0.917
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3799205-3799229	2	0.92
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	329365-329389	2	0.92
NZ_CP019798_1	1.1|1068254|24|NZ_CP019798|CRT	1068254-1068277	24	NC_018022	Mycolicibacterium chubuense NBB4 plasmid pMYCCH.01, complete sequence	269273-269296	3	0.875
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_013858	Azospirillum sp. B510 plasmid pAB510d, complete sequence	189095-189122	3	0.893
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	564591-564615	3	0.88
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP020701	Streptomyces tsukubensis strain NRRL 18488 plasmid pSTS1, complete sequence	8164-8188	3	0.88
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	801757-801784	4	0.857
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_LN831789	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE2	70454-70481	4	0.857
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_010429	Stenotrophomonas phage PSH1, complete sequence	3418-3445	4	0.857
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_048046	Caulobacter phage CcrPW, complete genome	56759-56786	4	0.857
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH588547	Caulobacter phage CcrSC, complete genome	69025-69052	4	0.857
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_LR134461	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 19, complete sequence	119917-119944	4	0.857
NZ_CP019798_9	9.2|4885829|28|NZ_CP019798|CRT	4885829-4885856	28	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	63921-63948	4	0.857
NZ_CP019798_9	9.2|4885829|28|NZ_CP019798|CRT	4885829-4885856	28	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	987388-987415	4	0.857
NZ_CP019798_9	9.2|4885829|28|NZ_CP019798|CRT	4885829-4885856	28	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1385064-1385091	4	0.857
NZ_CP019798_9	9.2|4885829|28|NZ_CP019798|CRT	4885829-4885856	28	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	644050-644077	4	0.857
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP033582	Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence	494351-494375	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	663026-663050	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NC_008269	Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence	1015638-1015662	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	115539-115563	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP011665	Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence	194200-194224	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	129613-129637	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	1614257-1614281	4	0.84
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP020331	Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence	239503-239527	4	0.84
NZ_CP019798_9	9.4|4885918|27|NZ_CP019798|CRT	4885918-4885944	27	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1735669-1735695	4	0.852
NZ_CP019798_9	9.4|4885918|27|NZ_CP019798|CRT	4885918-4885944	27	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	77452-77478	4	0.852
NZ_CP019798_9	9.4|4885918|27|NZ_CP019798|CRT	4885918-4885944	27	NZ_CP054029	Rhizobium sp. JKLM19E plasmid pPR19E02, complete sequence	331335-331361	4	0.852
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013526	Rhizobium phaseoli strain R744 plasmid pRphaR744d, complete sequence	698760-698789	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013556	Rhizobium phaseoli strain N931 plasmid pRphaN931d, complete sequence	728748-728777	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013589	Rhizobium phaseoli strain N161 plasmid pRphaN161d, complete sequence	717487-717516	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013531	Rhizobium phaseoli strain R723 plasmid pRphaR723d, complete sequence	690395-690424	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013541	Rhizobium phaseoli strain R630 plasmid pRphaR630d, complete sequence	715267-715296	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013567	Rhizobium phaseoli strain N831 plasmid pRphaN831d, complete sequence	728748-728777	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013584	Rhizobium phaseoli strain N261 plasmid pRphaN261d, complete sequence	690395-690424	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_010997	Rhizobium etli CIAT 652 plasmid pC, complete sequence	690930-690959	5	0.833
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013536	Rhizobium phaseoli strain R650 plasmid pRphaR650d, complete sequence	186884-186913	5	0.833
NZ_CP019798_1	1.6|1068488|30|NZ_CP019798|CRT	1068488-1068517	30	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1138667-1138696	5	0.833
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	503184-503211	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP029833	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence	173159-173186	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1673681-1673708	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP040452	Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence	1547625-1547652	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK310141	Mycobacterium phage Fenn, complete genome	29918-29945	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK524523	Mycobacterium phage Naira, complete genome	29965-29992	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP018096	Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence	425603-425630	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP018784	Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence	76763-76790	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP045074	Paracoccus kondratievae strain BJQ0001 plasmid unnamed1, complete sequence	193741-193768	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MF919500	Mycobacterium phage Dalmatian, complete genome	1518-1545	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK524490	Mycobacterium phage Donny, complete genome	31923-31950	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_019408	Caulobacter phage CcrRogue, complete genome	40472-40499	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KX576639	Mycobacterium phage DudeLittle, complete genome	1518-1545	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	JN699007	Mycobacterium phage Acadian, complete genome	31918-31945	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MT889381	Mycobacterium phage Suigeneris, complete genome	31923-31950	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MN234185	Mycobacterium phage Lemuria, complete genome	24351-24378	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_017957	Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence	505036-505063	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_019959	Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence	92145-92172	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP030764	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed4, complete sequence	324647-324674	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	414205-414232	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MT498055	Arthrobacter phage Bumble, complete genome	15598-15625	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	DQ372923	Bacteriophage mu1/6, complete genome	10802-10829	5	0.821
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_007967	Streptomyces phage mu1/6, complete genome	10802-10829	5	0.821
NZ_CP019798_3	3.2|2068234|31|NZ_CP019798|CRT	2068234-2068264	31	NZ_CP029776	Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed2, complete sequence	7730-7760	5	0.839
NZ_CP019798_8	8.1|4720748|26|NZ_CP019798|CRISPRCasFinder	4720748-4720773	26	DQ674738	Aeromonas phage phiO18P, complete genome	19747-19772	5	0.808
NZ_CP019798_9	9.2|4885829|28|NZ_CP019798|CRT	4885829-4885856	28	NZ_CP044550	Hydrogenophaga sp. BPS33 plasmid pBPS33-1, complete sequence	298730-298757	5	0.821
NZ_CP019798_9	9.3|4885875|25|NZ_CP019798|CRT	4885875-4885899	25	NZ_CP014798	Salipiger profundus strain JLT2016 plasmid pTPRO2, complete sequence	91583-91607	5	0.8
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP013562	Rhizobium phaseoli strain N841 plasmid pRphaN841e, complete sequence	704038-704067	6	0.8
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_048169	Gordonia phage BrutonGaster, complete genome	15885-15914	6	0.8
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_013858	Azospirillum sp. B510 plasmid pAB510d, complete sequence	395834-395861	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	391424-391451	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP015279	Mycobacterium chimaera strain DSM 44623 plasmid unnamed 1, complete sequence	63966-63993	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP015268	Mycobacterium chimaera strain ZUERICH-2 plasmid unnamed 1, complete sequence	16989-17016	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	541839-541866	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	947032-947059	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	626027-626054	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP023670	Methylomonas koyamae strain LM6 plasmid pLM6, complete sequence	103888-103915	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	200812-200839	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	HM486077	Tsukamurella phage TPA2, complete sequence	53473-53500	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_015210	Tsukamurella phage TPA2, complete genome	53473-53500	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	JX163858	Caulobacter phage phiCbK, complete genome	165371-165398	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP032326	Azospirillum brasilense strain MTCC4035 plasmid p5, complete sequence	155001-155028	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	412522-412549	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016110	Streptomyces pratensis ATCC 33331 plasmid pSFLA01, complete sequence	92817-92844	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP011053	Halomonas sp. KO116 plasmid unnamed1, complete sequence	22698-22725	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016586	Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence	320187-320214	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KY555147	Caulobacter phage Ccr34, complete genome	42425-42452	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KY555145	Caulobacter phage Ccr29, complete genome	45094-45121	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016655	Rhodococcus phage REQ1, complete genome	27842-27869	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MN617843	Mycobacterium phage Quesadilla, complete genome	34073-34100	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KY555146	Caulobacter phage Ccr32, complete genome	42459-42486	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_LT703507	Mycobacterium chimaera strain Mycobacterium chimaera MC045 isolate Mycobacterium chimaera plasmid 3	67256-67283	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP015273	Mycobacterium chimaera strain ZUERICH-1 plasmid unnamed 1, complete sequence	59480-59507	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1192013-1192040	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	719945-719972	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	5852101-5852128	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_020275	Mycobacterium intracellulare subsp. yongonense 05-1390 plasmid pMyong1, complete sequence	44720-44747	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP029333	Mycobacterium avium subsp. hominissuis strain MAC109 plasmid pMAC109a, complete sequence	108230-108257	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP045964	Mycobacterium chimaera strain AUSMDU00007395 plasmid pAUSMDU00007395_01, complete sequence	50723-50750	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_022654	Mycobacterium kansasii ATCC 12478 plasmid pMK12478, complete sequence	51263-51290	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	AP013464	Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C51-MedDCM-OCT-S31-C32	21239-21266	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP019465	Streptomyces autolyticus strain CGMCC0516 plasmid unnamed8, complete sequence	3242-3269	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP038236	Leisingera sp. NJS201 plasmid unnamed2, complete sequence	4041-4068	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_023316	Streptomyces sp. 14R-10 plasmid pZL1, complete sequence	32785-32812	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP015280	Mycobacterium chimaera strain DSM 44623 plasmid unnamed 2, complete sequence	40855-40882	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	2435295-2435322	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP023153	Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_2, complete sequence	28492-28519	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1093130-1093157	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP019224	Mycobacterium chimaera strain CDC 2015-22-71 plasmid pDHQP20152271_1, complete sequence	73597-73624	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	607831-607858	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP017104	Rhizobium gallicum strain IE4872 plasmid pRgalIE4872c, complete sequence	457553-457580	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH479919	Mycobacterium phage Moose, complete genome	28454-28481	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MG925342	Mycobacterium phage Forsytheast, complete genome	28454-28481	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK112532	Mycobacterium phage Bones, complete genome	28117-28144	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MT522000	Mycobacterium phage Soul22, complete genome	21845-21872	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MN735431	Mycobacterium phage Hegedechwinu, complete genome	12421-12448	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MG925340	Mycobacterium phage Corvo, complete genome	29176-29203	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_042030	Mycobacterium phage Yoshi, complete sequence	21846-21873	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH669002	Mycobacterium phage Emmina, complete genome	26719-26746	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KR080198	Mycobacterium phage Cambiare, complete genome	25013-25040	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_048729	Mycobacterium phage Renaud18, complete genome	22518-22545	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	JN859129	Mycobacterium virus DotProduct, complete genome	12551-12578	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH727561	Mycobacterium phage Serendipitous, complete genome	31769-31796	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	JN398369	Mycobacterium phage RidgeCB, complete genome	28022-28049	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH450133	Mycobacterium phage SwissCheese, complete genome	28954-28981	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KF560331	Mycobacterium phage Graduation, complete genome	28937-28964	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK494105	Mycobacterium phage Pinnie, complete genome	24696-24723	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH509447	Microbacterium phage Eden, complete genome	2291-2318	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH077585	Mycobacterium phage TChen, complete genome	22623-22650	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK359316	Mycobacterium phage Cueylyss, complete genome	28350-28377	6	0.786
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_048788	Mycobacterium phage ThetaBob, complete genome	22436-22463	6	0.786
NZ_CP019798_9	9.4|4885918|27|NZ_CP019798|CRT	4885918-4885944	27	NZ_CP036456	Streptomonospora sp. M2 plasmid phiM2, complete sequence	75342-75368	6	0.778
NZ_CP019798_9	9.5|4885963|28|NZ_CP019798|CRT	4885963-4885990	28	MN585972	Arthrobacter phage Edmundo, complete genome	3187-3214	6	0.786
NZ_CP019798_9	9.6|4886009|28|NZ_CP019798|CRT	4886009-4886036	28	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	670671-670698	6	0.786
NZ_CP019798_9	9.6|4886009|28|NZ_CP019798|CRT	4886009-4886036	28	NZ_CP050101	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b6, complete sequence	228868-228895	6	0.786
NZ_CP019798_9	9.6|4886009|28|NZ_CP019798|CRT	4886009-4886036	28	NZ_AP017899	Sphingopyxis sp. FD7 plasmid pSFD01, complete sequence	101782-101809	6	0.786
NZ_CP019798_9	9.6|4886009|28|NZ_CP019798|CRT	4886009-4886036	28	NZ_CP053442	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eD, complete sequence	228133-228160	6	0.786
NZ_CP019798_9	9.6|4886009|28|NZ_CP019798|CRT	4886009-4886036	28	NZ_CP017148	Bosea vaviloviae strain Vaf18 plasmid unnamed1, complete sequence	305574-305601	6	0.786
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP025017	Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence	257686-257715	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	29817-29846	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP024986	Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence	166635-166664	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_013859	Azospirillum sp. B510 plasmid pAB510e, complete sequence	180480-180509	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP054026	Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence	1941-1970	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP054620	Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence	349746-349775	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP045548	Streptomyces sp. SYP-A7193 plasmid unnamed1, complete sequence	180923-180952	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK919470	Gordonia phage Mellie, complete genome	27641-27670	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_024970	Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence	74413-74442	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_KJ396772	Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence	74413-74442	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP016291	Rhizobium leguminosarum strain Vaf10 plasmid unnamed6, complete sequence	145647-145676	7	0.767
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_016624	Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence	338946-338975	7	0.767
NZ_CP019798_1	1.6|1068488|30|NZ_CP019798|CRT	1068488-1068517	30	NC_013502	Rhodothermus marinus DSM 4252 plasmid pRMAR01, complete sequence	14414-14443	7	0.767
NZ_CP019798_1	1.6|1068488|30|NZ_CP019798|CRT	1068488-1068517	30	NZ_CP003988	Streptomyces sp. 769 plasmid pSGZL, complete sequence	99762-99791	7	0.767
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	489927-489958	7	0.781
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	629581-629612	7	0.781
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1307611-1307642	7	0.781
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	824761-824792	7	0.781
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	774369-774396	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	1010182-1010209	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	41549-41576	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	243341-243368	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	666422-666449	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK416018	Klebsiella phage ST147-VIM1phi7.1, complete genome	11812-11839	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_008760	Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence	113184-113211	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_008758	Polaromonas naphthalenivorans CJ2 plasmid pPNAP02, complete sequence	144234-144261	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_008758	Polaromonas naphthalenivorans CJ2 plasmid pPNAP02, complete sequence	144174-144201	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	CP000876	Herpetosiphon aurantiacus DSM 785 plasmid pHAU01, complete sequence	146837-146864	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP018064	Rhodococcus sp. 2G plasmid p1, complete sequence	165527-165554	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP030264	Ensifer adhaerens strain Corn53 plasmid AB, complete sequence	400315-400342	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	1115076-1115103	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	834838-834865	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP016619	Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence	663821-663848	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP038031	Rhodococcus ruber strain R1 plasmid unnamed1, complete sequence	81476-81503	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1297546-1297573	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK977696	Gordonia phage SCentae, complete genome	45723-45750	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK977695	Gordonia phage Pupper, complete genome	45577-45604	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_015951	Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence	285706-285733	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP040720	Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence	2979-3006	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP032678	Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence	71227-71254	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP025436	Gordonia sp. YC-JH1 plasmid pGOR1, complete sequence	68219-68246	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP016821	Rhodococcus sp. p52 plasmid pDF01, complete sequence	56907-56934	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP047177	Rathayibacter sp. VKM Ac-2759 plasmid unnamed1, complete sequence	108568-108595	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KY883642	Vibrio phage JSF15, complete genome	30875-30902	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	KY883656	Vibrio phage JSF9, complete genome	26550-26577	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MN234183	Mycobacterium phage Antsirabe, complete genome	24515-24542	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_022070	Mycobacteriophage Wheeler, complete genome	28977-29004	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MF141540	Mycobacterium phage Avocado, complete genome	24542-24569	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK937593	Mycobacterium phage Flypotenuse, complete genome	26504-26531	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH588544	Caulobacter phage CcrBL10, complete genome	59652-59679	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_026585	Mycobacteriophage Estave1, complete genome	22211-22238	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MH536820	Mycobacterium phage Glexan, complete genome	26504-26531	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MK801726	Mycobacterium phage ChotaBhai, complete genome	26137-26164	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	MG925349	Mycobacterium phage Mendokysei, complete genome	22301-22328	7	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NC_031109	Gordonia phage Jumbo, complete genome	37109-37136	7	0.75
NZ_CP019798_3	3.2|2068234|31|NZ_CP019798|CRT	2068234-2068264	31	NZ_CP033583	Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence	98958-98988	7	0.774
NZ_CP019798_9	9.5|4885963|28|NZ_CP019798|CRT	4885963-4885990	28	NZ_AF135182	Serratia entomophila strain A1MO2 plasmid pADAP, complete sequence	1962-1989	7	0.75
NZ_CP019798_9	9.5|4885963|28|NZ_CP019798|CRT	4885963-4885990	28	NC_002523	Serratia entomophila plasmid pADAP, complete sequence	1962-1989	7	0.75
NZ_CP019798_1	1.4|1068386|36|NZ_CP019798|CRT	1068386-1068421	36	ASHF01000034	Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence	45978-46013	8	0.778
NZ_CP019798_1	1.4|1068386|36|NZ_CP019798|CRT	1068386-1068421	36	NZ_CP011276	Planctomyces sp. SH-PL62 plasmid pPL62-3, complete sequence	59311-59346	8	0.778
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	2004717-2004746	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	112107-112136	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	502579-502608	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP026091	Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence	518936-518965	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP046569	Dietzia sp. DQ12-45-1b plasmid pII, complete sequence	38618-38647	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP026093	Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence	518962-518991	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	548372-548401	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1701012-1701041	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP021357	Rhodococcus sp. S2-17 plasmid pRB11, complete sequence	60509-60538	8	0.733
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	799905-799934	8	0.733
NZ_CP019798_1	1.6|1068488|30|NZ_CP019798|CRT	1068488-1068517	30	NZ_CP049042	Pseudohalocynthiibacter aestuariivivens strain RR4-35 plasmid pRR4-35_5, complete sequence	54134-54163	8	0.733
NZ_CP019798_1	1.6|1068488|30|NZ_CP019798|CRT	1068488-1068517	30	NZ_CP049142	Pseudomonas nitroreducens strain HBP1 plasmid pPniHBP1_1, complete sequence	334623-334652	8	0.733
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	226236-226267	8	0.75
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP053565	Pseudonocardia sp. Gen01 plasmid unnamed1, complete sequence	31377-31408	8	0.75
NZ_CP019798_3	3.1|2068186|28|NZ_CP019798|CRT	2068186-2068213	28	NZ_CP013071	Sphingobium indicum B90A plasmid pSRL1, complete sequence	71371-71398	8	0.714
NZ_CP019798_3	3.2|2068234|31|NZ_CP019798|CRT	2068234-2068264	31	NZ_CP040819	Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence	412130-412160	8	0.742
NZ_CP019798_3	3.2|2068234|31|NZ_CP019798|CRT	2068234-2068264	31	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	147489-147519	8	0.742
NZ_CP019798_1	1.4|1068386|36|NZ_CP019798|CRT	1068386-1068421	36	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1094642-1094677	9	0.75
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK977708	Mycobacterium phage Fulbright, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KU935731	Mycobacterium phage Phrann, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MT498048	Mycobacterium phage Raymond7, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MG099948	Mycobacterium phage Philonius, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MH926055	Mycobacterium phage Chewbacca, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524522	Mycobacterium phage Purgamenstris, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MT723932	Mycobacterium phage Schnauzer, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KU935726	Mycobacterium phage Xerxes, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MT684588	Mycobacterium phage Snekmaggedon, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MT498042	Mycobacterium phage Rebel, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MT498044	Mycobacterium phage Jamie19, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KU935730	Mycobacterium phage Pipsqueaks, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KX756439	Mycobacterium phage PhancyPhin, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MH316570	Mycobacterium phage Silvafighter, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524518	Mycobacterium phage Smurph, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK392367	Mycobacterium phage BabeRuth, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524520	Mycobacterium phage Nenae, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524515	Mycobacterium phage Parmesanjohn, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MH697585	Mycobacterium phage Gex, complete genome	10605-10634	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KM588359	Mycobacterium phage Carcharodon, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MH697576	Mycobacterium phage Aggie, complete genome	10607-10636	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MH697593	Mycobacterium phage Tapioca, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	JN624851	Mycobacterium phage Redi, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KU935727	Mycobacterium phage Panchino, complete genome	10628-10657	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	KU935729	Mycobacterium phage SkinnyPete, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MG099936	Mycobacterium phage Andies, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NC_031243	Mycobacterium phage Xeno, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524509	Mycobacterium phage SpongeBob, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	MK524528	Mycobacterium phage ShrimpFriedEgg, complete genome	10652-10681	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	JN256079	Mycobacterium phage Charlie, complete genome	10606-10635	9	0.7
NZ_CP019798_1	1.5|1068440|30|NZ_CP019798|CRT	1068440-1068469	30	NZ_CP024314	Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence	1961749-1961778	9	0.7
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	1630682-1630713	9	0.719
NZ_CP019798_2	2.1|1129052|32|NZ_CP019798|CRISPRCasFinder	1129052-1129083	32	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	1433679-1433710	9	0.719

1. spacer 1.1|1068254|24|NZ_CP019798|CRT matches to NC_019959 (Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence) position: , mismatch: 2, identity: 0.917

cccgacggcgtcggcggttccgac	CRISPR spacer
cccgccggcggcggcggttccgac	Protospacer
**** ***** *************

2. spacer 1.1|1068254|24|NZ_CP019798|CRT matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 2, identity: 0.917

cccgacggcgtcggcggttccgac	CRISPR spacer
cgcgacgtcgtcggcggttccgac	Protospacer
* ***** ****************

3. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 2, identity: 0.92

accctccggctcggcgccgggcccg	CRISPR spacer
accctccggctcggcgcccgggccg	Protospacer
****************** ** ***

4. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 2, identity: 0.92

accctccggctcggcgccgggcccg	CRISPR spacer
accctccgggtcagcgccgggcccg	Protospacer
********* **.************

5. spacer 1.1|1068254|24|NZ_CP019798|CRT matches to NC_018022 (Mycolicibacterium chubuense NBB4 plasmid pMYCCH.01, complete sequence) position: , mismatch: 3, identity: 0.875

cccgacggcgtcggcggttccgac	CRISPR spacer
gccgacggcgtcggcggggccgac	Protospacer
 ****************  *****

6. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_013858 (Azospirillum sp. B510 plasmid pAB510d, complete sequence) position: , mismatch: 3, identity: 0.893

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gggagccgccgccgccgccggagccggg	Protospacer
** **********.*************.

7. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 3, identity: 0.88

accctccggctcggcgccgggcccg	CRISPR spacer
gccctccggcgcggcgccgggaccg	Protospacer
.********* ********** ***

8. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP020701 (Streptomyces tsukubensis strain NRRL 18488 plasmid pSTS1, complete sequence) position: , mismatch: 3, identity: 0.88

accctccggctcggcgccgggcccg	CRISPR spacer
atcctccggttcagcgccgggcccg	Protospacer
*.*******.**.************

9. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtggccgccgcctccgccggagccggc	Protospacer
 **.********* ************* 

10. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_LN831789 (Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE2) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tggagccgccgccaccggaggagccgga	Protospacer
 * **************  *********

11. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_010429 (Stenotrophomonas phage PSH1, complete sequence) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgcagctgccgccaccgccgaagccgga	Protospacer
 *.***.*************.*******

12. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_048046 (Caulobacter phage CcrPW, complete genome) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agtagccgccgccaccgccgccgccgca	Protospacer
.*******************  **** *

13. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH588547 (Caulobacter phage CcrSC, complete genome) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agtagccgccgccaccgccgccgccgca	Protospacer
.*******************  **** *

14. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_LR134461 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 19, complete sequence) position: , mismatch: 4, identity: 0.857

ggtagccgccgccaccgccggagccgga---	CRISPR spacer
ggtagccgccgccaccgcc---gccgggacg	Protospacer
*******************   *****.   

15. spacer 9.2|4885829|28|NZ_CP019798|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 4, identity: 0.857

gtacggctcgctcctggcgggggtgtcg	CRISPR spacer
gtacggcgcgctcctggcggcggtcgcg	Protospacer
******* ************ ***  **

16. spacer 9.2|4885829|28|NZ_CP019798|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 4, identity: 0.857

gtacggctcgctcctggcgggggtgtcg	CRISPR spacer
gtacggcgcgctcctggcggcggtcgcg	Protospacer
******* ************ ***  **

17. spacer 9.2|4885829|28|NZ_CP019798|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 4, identity: 0.857

gtacggctcgctcctggcgggggtgtcg	CRISPR spacer
gtacggcgcgctcctggcggcggtcgcg	Protospacer
******* ************ ***  **

18. spacer 9.2|4885829|28|NZ_CP019798|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 4, identity: 0.857

gtacggctcgctcctggcgggggtgtcg	CRISPR spacer
gtacggcgcgctcctggcggcggtcgcg	Protospacer
******* ************ ***  **

19. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP033582 (Streptomyces sp. ADI95-16 plasmid pADI95-16a, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
cacctccggctgggcgcccggcccg	Protospacer
  ********* ****** ******

20. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
accggccggctcggcgccgggccga	Protospacer
***  ****************** .

21. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NC_008269 (Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
accccccggctcggcgccggggcga	Protospacer
****.**************** * .

22. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
ggcctccgggtcggtgccgggcccg	Protospacer
. ******* ****.**********

23. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP011665 (Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
cacctccggctgggcgcccggcccg	Protospacer
  ********* ****** ******

24. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
cacctccggcccggcgccgggccgg	Protospacer
  ********.************ *

25. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
gccctcctgctcggcgccggggcca	Protospacer
.****** ************* **.

26. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP020331 (Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence) position: , mismatch: 4, identity: 0.84

accctccggctcggcgccgggcccg	CRISPR spacer
ctcctccggcccggcgccgggcgcg	Protospacer
 .********.*********** **

27. spacer 9.4|4885918|27|NZ_CP019798|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 4, identity: 0.852

gtgcggctggatccgggcggggtgtcg	CRISPR spacer
gtgcggctggatccggccggcgttgcg	Protospacer
**************** *** **  **

28. spacer 9.4|4885918|27|NZ_CP019798|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 4, identity: 0.852

gtgcggctggatccgggcggggtgtcg	CRISPR spacer
gtgcggctggatccggccggcgttgcg	Protospacer
**************** *** **  **

29. spacer 9.4|4885918|27|NZ_CP019798|CRT matches to NZ_CP054029 (Rhizobium sp. JKLM19E plasmid pPR19E02, complete sequence) position: , mismatch: 4, identity: 0.852

gtgcggctggatccgggcggggtgtcg-	CRISPR spacer
gtgcggctggatccggac-gggcgccgg	Protospacer
****************.* ***.*.** 

30. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013526 (Rhizobium phaseoli strain R744 plasmid pRphaR744d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

31. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013556 (Rhizobium phaseoli strain N931 plasmid pRphaN931d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

32. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013589 (Rhizobium phaseoli strain N161 plasmid pRphaN161d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

33. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013531 (Rhizobium phaseoli strain R723 plasmid pRphaR723d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

34. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013541 (Rhizobium phaseoli strain R630 plasmid pRphaR630d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

35. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013567 (Rhizobium phaseoli strain N831 plasmid pRphaN831d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

36. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013584 (Rhizobium phaseoli strain N261 plasmid pRphaN261d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

37. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_010997 (Rhizobium etli CIAT 652 plasmid pC, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

38. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013536 (Rhizobium phaseoli strain R650 plasmid pRphaR650d, complete sequence) position: , mismatch: 5, identity: 0.833

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaaaccggc	Protospacer
* ***.****************** ***. 

39. spacer 1.6|1068488|30|NZ_CP019798|CRT matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

ttcgacggcgactgcgatcccgagtgcgtg-	CRISPR spacer
ctctacggcgacggcgatcccgag-gcgagc	Protospacer
.** ******** *********** *** * 

40. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctgcgccgccgacaccgccggagccgga	Protospacer
    ******* ****************

41. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP029833 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctgcgccgccgacaccgccggagccgga	Protospacer
    ******* ****************

42. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtagctgccgccaccgccgtagccgcc	Protospacer
 *****.************* *****  

43. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP040452 (Halomonas sp. PA16-9 plasmid p_unnamed1, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agtagccgcctccaccgccgtagccgct	Protospacer
.********* ********* *****  

44. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK310141 (Mycobacterium phage Fenn, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgtagccgccgccaccgccgccgccgcc	Protospacer
 *******************  ****  

45. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK524523 (Mycobacterium phage Naira, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgtagccgccgccaccgccgccgccgcc	Protospacer
 *******************  ****  

46. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP018096 (Chelatococcus daeguensis strain TAD1 plasmid pTAD1, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtgaccgccgcctccgccggagccggc	Protospacer
 **..******** ************* 

47. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP018784 (Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ggtagccgccgccaccaccggacgctgc	Protospacer
****************.*****  * * 

48. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP045074 (Paracoccus kondratievae strain BJQ0001 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gcccgccgccgccaccgccgccgccgga	Protospacer
* . ****************  ******

49. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MF919500 (Mycobacterium phage Dalmatian, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
actggctaccgccaccgccggagccgga	Protospacer
. *.**..********************

50. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK524490 (Mycobacterium phage Donny, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccaccgccgccgccgga	Protospacer
 *. ****************  ******

51. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_019408 (Caulobacter phage CcrRogue, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agtagccgccgccaccgccgccgcccgc	Protospacer
.*******************  *** * 

52. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KX576639 (Mycobacterium phage DudeLittle, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
actggctaccgccaccgccggagccgga	Protospacer
. *.**..********************

53. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to JN699007 (Mycobacterium phage Acadian, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccaccgccgccgccgga	Protospacer
 *. ****************  ******

54. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MT889381 (Mycobacterium phage Suigeneris, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccaccgccgccgccgga	Protospacer
 *. ****************  ******

55. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MN234185 (Mycobacterium phage Lemuria, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccaccaccggcgccgga	Protospacer
 *. ************.**** ******

56. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_017957 (Tistrella mobilis KA081020-065 plasmid pTM1, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctggccgccgccgccgccggggccggc	Protospacer
* *.*********.*******.***** 

57. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_019959 (Mycobacterium sp. JS623 plasmid pMYCSM03, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgcagttgccgccaccgccggtgccgga	Protospacer
 *.**..************** ******

58. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP030764 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed4, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgaagccgccgccaccgccgacgccgaa	Protospacer
 * *****************. ****.*

59. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ggctcccgccgccaccgccagagcggga	Protospacer
**.  **************.**** ***

60. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MT498055 (Arthrobacter phage Bumble, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtccccgccgccccctccggagccgga	Protospacer
 **  ******** ** ***********

61. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to DQ372923 (Bacteriophage mu1/6, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ggaggccgccgccccggccggagccggg	Protospacer
** .********* * ***********.

62. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_007967 (Streptomyces phage mu1/6, complete genome) position: , mismatch: 5, identity: 0.821

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ggaggccgccgccccggccggagccggg	Protospacer
** .********* * ***********.

63. spacer 3.2|2068234|31|NZ_CP019798|CRT matches to NZ_CP029776 (Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.839

cgctgcccgagccggagccgcggtagccacc--	CRISPR spacer
cgctgcccgagccggacctgcgg--gccgccct	Protospacer
**************** *.****  ***.**  

64. spacer 8.1|4720748|26|NZ_CP019798|CRISPRCasFinder matches to DQ674738 (Aeromonas phage phiO18P, complete genome) position: , mismatch: 5, identity: 0.808

tcttgggccggacataggccgccacc	CRISPR spacer
cggtgggcaggacataggccgccgcc	Protospacer
.  ***** **************.**

65. spacer 9.2|4885829|28|NZ_CP019798|CRT matches to NZ_CP044550 (Hydrogenophaga sp. BPS33 plasmid pBPS33-1, complete sequence) position: , mismatch: 5, identity: 0.821

gtacggctcgctcctggcgggggtgtcg	CRISPR spacer
ggacggctcgctcctggcggggtttgcc	Protospacer
* ******************** *  * 

66. spacer 9.3|4885875|25|NZ_CP019798|CRT matches to NZ_CP014798 (Salipiger profundus strain JLT2016 plasmid pTPRO2, complete sequence) position: , mismatch: 5, identity: 0.8

accctccggctcggcgccgggcccg	CRISPR spacer
cacctccggctcggcgccgggcaga	Protospacer
  ********************  .

67. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP013562 (Rhizobium phaseoli strain N841 plasmid pRphaN841e, complete sequence) position: , mismatch: 6, identity: 0.8

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gtcgagccggagggcgtcggcgaactggcc	Protospacer
* ***.*******************. *  

68. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_048169 (Gordonia phage BrutonGaster, complete genome) position: , mismatch: 6, identity: 0.8

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaaccggagggcgacgacgaccgggaa	Protospacer
**************** **.*** *  **.

69. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_013858 (Azospirillum sp. B510 plasmid pAB510d, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctgcgccgccgacaccgccggtgccgga	Protospacer
    ******* ********* ******

70. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aggagccgcccccgccgccggagccgcc	Protospacer
.* ******* **.************  

71. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP015279 (Mycobacterium chimaera strain DSM 44623 plasmid unnamed 1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ccgcgccgccgccaccgccggcgccggc	Protospacer
    ***************** ***** 

72. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP015268 (Mycobacterium chimaera strain ZUERICH-2 plasmid unnamed 1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ccgcgccgccgccaccgccggcgccggc	Protospacer
    ***************** ***** 

73. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccgccgccggagccgcc	Protospacer
 *. *********.************  

74. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tccagccaccgccaccgcccgagccggg	Protospacer
  .****.*********** *******.

75. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctacgccgccgcgaccgcctgagccgga	Protospacer
    ******** ****** ********

76. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP023670 (Methylomonas koyamae strain LM6 plasmid pLM6, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtagccgccgccaccgccgaatcctcc	Protospacer
 *******************.* **   

77. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctgcgccgccgacaccgccggtgccgga	Protospacer
    ******* ********* ******

78. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to HM486077 (Tsukamurella phage TPA2, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gaggcccgccgccaccgcctgagccggg	Protospacer
*. . ************** *******.

79. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_015210 (Tsukamurella phage TPA2, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gaggcccgccgccaccgcctgagccggg	Protospacer
*. . ************** *******.

80. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to JX163858 (Caulobacter phage phiCbK, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aatagccgccgccgccgccgcagccgtt	Protospacer
..***********.****** *****  

81. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP032326 (Azospirillum brasilense strain MTCC4035 plasmid p5, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccaccgccaccgccggagccgcc	Protospacer
 *. ***.******************  

82. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggcgccgcctccaccgccggagccgcc	Protospacer
 *  ****** ***************  

83. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016110 (Streptomyces pratensis ATCC 33331 plasmid pSFLA01, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tcgagcctccgccaccgccggatccggt	Protospacer
   **** ************** **** 

84. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP011053 (Halomonas sp. KO116 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agccgccgccgccaccgccgaagccgcc	Protospacer
.*. ****************.*****  

85. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016586 (Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aggagccgccgccaccgcccgcgccgac	Protospacer
.* **************** * ****. 

86. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KY555147 (Caulobacter phage Ccr34, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aatagccgccgccgccgccgcagccgtt	Protospacer
..***********.****** *****  

87. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KY555145 (Caulobacter phage Ccr29, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aatagccgccgccgccgccgcagccgtt	Protospacer
..***********.****** *****  

88. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016655 (Rhodococcus phage REQ1, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agcctgcgccgccgccgccggagccgga	Protospacer
.*.   *******.**************

89. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MN617843 (Mycobacterium phage Quesadilla, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
actgcccgccgcctccgccggagccggt	Protospacer
. *. ******** ************* 

90. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KY555146 (Caulobacter phage Ccr32, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
aatagccgccgccgccgccgcagccgtt	Protospacer
..***********.****** *****  

91. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_LT703507 (Mycobacterium chimaera strain Mycobacterium chimaera MC045 isolate Mycobacterium chimaera plasmid 3) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

92. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP015273 (Mycobacterium chimaera strain ZUERICH-1 plasmid unnamed 1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

93. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgctgccgccgcctccgcaggagccggt	Protospacer
 *. ********* **** ******** 

94. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgcagccaccgccaccgccggcgccgcc	Protospacer
 *.****.************* ****  

95. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgaagccgccaccaccgccgaagccgcc	Protospacer
 * *******.*********.*****  

96. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_020275 (Mycobacterium intracellulare subsp. yongonense 05-1390 plasmid pMyong1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

97. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP029333 (Mycobacterium avium subsp. hominissuis strain MAC109 plasmid pMAC109a, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

98. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP045964 (Mycobacterium chimaera strain AUSMDU00007395 plasmid pAUSMDU00007395_01, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

99. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_022654 (Mycobacterium kansasii ATCC 12478 plasmid pMK12478, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

100. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to AP013464 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G18, isolate: uvMED-CGR-C51-MedDCM-OCT-S31-C32) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgcagccgccggcaccaccggagccgcc	Protospacer
 *.******** ****.*********  

101. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP019465 (Streptomyces autolyticus strain CGMCC0516 plasmid unnamed8, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgcggccgccgcgaccgccggggccggc	Protospacer
 *..******** ********.***** 

102. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP038236 (Leisingera sp. NJS201 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgaagcggctgccaccgccggagccgtg	Protospacer
 * *** **.**************** .

103. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_023316 (Streptomyces sp. 14R-10 plasmid pZL1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
agctcccgcccccgccgccggagccgga	Protospacer
.*.  ***** **.**************

104. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP015280 (Mycobacterium chimaera strain DSM 44623 plasmid unnamed 2, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

105. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgctgccgccgcctccgcaggagccggt	Protospacer
 *. ********* **** ******** 

106. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP023153 (Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_2, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

107. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgcagccaccgccaccgccggcgccgcc	Protospacer
 *.****.************* ****  

108. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP019224 (Mycobacterium chimaera strain CDC 2015-22-71 plasmid pDHQP20152271_1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gctcaccgccgccaccgccggggccgcg	Protospacer
* * .****************.**** .

109. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tctggccgccgccgccgccgcagccggc	Protospacer
  *.*********.****** ****** 

110. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP017104 (Rhizobium gallicum strain IE4872 plasmid pRgalIE4872c, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gagcgcagccgccaccaccggagccggc	Protospacer
*.  ** *********.********** 

111. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH479919 (Mycobacterium phage Moose, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

112. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MG925342 (Mycobacterium phage Forsytheast, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

113. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK112532 (Mycobacterium phage Bones, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

114. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MT522000 (Mycobacterium phage Soul22, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

115. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MN735431 (Mycobacterium phage Hegedechwinu, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtccatgccgacaccgccggagccgga	Protospacer
 **   .**** ****************

116. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MG925340 (Mycobacterium phage Corvo, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

117. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_042030 (Mycobacterium phage Yoshi, complete sequence) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

118. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH669002 (Mycobacterium phage Emmina, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccagagccgcc	Protospacer
 * *************.**.******  

119. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KR080198 (Mycobacterium phage Cambiare, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ccttgccgccgccaccgccgccgccggc	Protospacer
  * ****************  ***** 

120. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_048729 (Mycobacterium phage Renaud18, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

121. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to JN859129 (Mycobacterium virus DotProduct, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgtccatgccgacaccgccggagccgga	Protospacer
 **   .**** ****************

122. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH727561 (Mycobacterium phage Serendipitous, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccaccgccgccaccgccggaggcgta	Protospacer
 *. .****************** ** *

123. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to JN398369 (Mycobacterium phage RidgeCB, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

124. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH450133 (Mycobacterium phage SwissCheese, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

125. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KF560331 (Mycobacterium phage Graduation, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

126. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK494105 (Mycobacterium phage Pinnie, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccaccgccaccgccggcgccggc	Protospacer
 *. ***.************* ***** 

127. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH509447 (Microbacterium phage Eden, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gcgagccgccgacaccgcctgagccgtg	Protospacer
*  ******** ******* ****** .

128. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH077585 (Mycobacterium phage TChen, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

129. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK359316 (Mycobacterium phage Cueylyss, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

130. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_048788 (Mycobacterium phage ThetaBob, complete genome) position: , mismatch: 6, identity: 0.786

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cggagccgccgccaccaccggcgccgcc	Protospacer
 * *************.**** ****  

131. spacer 9.4|4885918|27|NZ_CP019798|CRT matches to NZ_CP036456 (Streptomonospora sp. M2 plasmid phiM2, complete sequence) position: , mismatch: 6, identity: 0.778

gtgcggctggatccgggcggggtgtcg	CRISPR spacer
cgccggctgggtccgggcgggctgtca	Protospacer
   *******.********** ****.

132. spacer 9.5|4885963|28|NZ_CP019798|CRT matches to MN585972 (Arthrobacter phage Edmundo, complete genome) position: , mismatch: 6, identity: 0.786

cccctgggcggggttactgcgggtgccc	CRISPR spacer
gctatgggcggggctactgcgggggcct	Protospacer
 *. *********.********* ***.

133. spacer 9.6|4886009|28|NZ_CP019798|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 6, identity: 0.786

gtgcggccggatcccggcaggggtgtcg	CRISPR spacer
gtgcggccggatcccagcaggcccgaca	Protospacer
***************.*****  .* *.

134. spacer 9.6|4886009|28|NZ_CP019798|CRT matches to NZ_CP050101 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b6, complete sequence) position: , mismatch: 6, identity: 0.786

gtgcggccggatcccggcaggggtgtcg	CRISPR spacer
gtgcggccggatcccagtagggggcgcc	Protospacer
***************.*.*****   * 

135. spacer 9.6|4886009|28|NZ_CP019798|CRT matches to NZ_AP017899 (Sphingopyxis sp. FD7 plasmid pSFD01, complete sequence) position: , mismatch: 6, identity: 0.786

gtgcggccggatcccggcaggggtgtcg	CRISPR spacer
ctcgcgccggatcccggcaagtgtgtcg	Protospacer
 *   **************.* ******

136. spacer 9.6|4886009|28|NZ_CP019798|CRT matches to NZ_CP053442 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eD, complete sequence) position: , mismatch: 6, identity: 0.786

gtgcggccggatcccggcaggggtgtcg	CRISPR spacer
gtgcggccggatcccagtagggggcgcc	Protospacer
***************.*.*****   * 

137. spacer 9.6|4886009|28|NZ_CP019798|CRT matches to NZ_CP017148 (Bosea vaviloviae strain Vaf18 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.786

gtgcggccggatcccggcaggggtgtcg	CRISPR spacer
gcgcggccggatccgggcaggggagggc	Protospacer
*.************ ******** *   

138. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP025017 (Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggggaaccagagggcgtcggcgatgtagac	Protospacer
** *****.**************  . ** 

139. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaacaggaaggcgtcggcgatgtcggc	Protospacer
******* ***.***********  .**. 

140. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP024986 (Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaaccggaggacgtcgccgacgtggtg	Protospacer
*************.***** ***  . * *

141. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_013859 (Azospirillum sp. B510 plasmid pAB510e, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaacaggaaggcgtcggcgatgtcggc	Protospacer
******* ***.***********  .**. 

142. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP054026 (Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggggaaccagagggcgtcggcgatgtagac	Protospacer
** *****.**************  . ** 

143. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP054620 (Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaactggaaggcgtcggcgatgtcggc	Protospacer
*******.***.***********  .**. 

144. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP045548 (Streptomyces sp. SYP-A7193 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggccgcgacgagggcggcggcgaacccgag	Protospacer
*** .    ******* *************

145. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK919470 (Gordonia phage Mellie, complete genome) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgacccggagggcgtcgtcgaccactgc	Protospacer
***** ************* *** * * . 

146. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_024970 (Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaaccggaggacgtcgccgacgtggtg	Protospacer
*************.***** ***  . * *

147. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_KJ396772 (Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaaccggaggacgtcgccgacgtggtg	Protospacer
*************.***** ***  . * *

148. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP016291 (Rhizobium leguminosarum strain Vaf10 plasmid unnamed6, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggggaaccagagggcgtcggcgatgtagac	Protospacer
** *****.**************  . ** 

149. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_016624 (Azospirillum lipoferum 4B plasmid AZO_p5, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaacaggaaggcgtcggcgatgtcggc	Protospacer
******* ***.***********  .**. 

150. spacer 1.6|1068488|30|NZ_CP019798|CRT matches to NC_013502 (Rhodothermus marinus DSM 4252 plasmid pRMAR01, complete sequence) position: , mismatch: 7, identity: 0.767

ttcgacggcgactgcgatcccgagtgcgtg	CRISPR spacer
aacgacggcgactgggatcccgagcgagat	Protospacer
  ************ *********.* *  

151. spacer 1.6|1068488|30|NZ_CP019798|CRT matches to NZ_CP003988 (Streptomyces sp. 769 plasmid pSGZL, complete sequence) position: , mismatch: 7, identity: 0.767

ttcgacggcgactgcgatcccgagtgcgtg	CRISPR spacer
tacgacggcgactccgatcccgagatggac	Protospacer
* *********** **********   *  

152. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.781

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
gagcggagccgcccttgccgggcggcgggccg	Protospacer
*. ******************* ***  **  

153. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 7, identity: 0.781

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
gagcggagccgcccttgccgggcggcgggccg	Protospacer
*. ******************* ***  **  

154. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.781

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
gagcggagccgcccttgccgggcggcgggctg	Protospacer
*. ******************* ***  **  

155. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 7, identity: 0.781

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
gagcggagccgcccttgccgggcggcgggctg	Protospacer
*. ******************* ***  **  

156. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tcattccgccgcgaccgccggcgccgga	Protospacer
     ******* ******** ******

157. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ttctgccgccgccaccgccggaggcgcg	Protospacer
  . ******************* ** .

158. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ttctgccgccgccaccgccggaggcgcg	Protospacer
  . ******************* ** .

159. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctgctccgccgccacggccggagcggga	Protospacer
     ********** ******** ***

160. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ttctgccgccgccaccgccggaggcgcg	Protospacer
  . ******************* ** .

161. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK416018 (Klebsiella phage ST147-VIM1phi7.1, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tcccggagccgccaccgccggagccggt	Protospacer
  . *  ******************** 

162. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_008760 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tatagccgccgccaccgccagagcgatc	Protospacer
 .*****************.**** .  

163. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_008758 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP02, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
catagccgccgccaccgccagagcgatc	Protospacer
 .*****************.**** .  

164. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_008758 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP02, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccaccgccgccaccgccgaagccgcc	Protospacer
 *. .***************.*****  

165. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to CP000876 (Herpetosiphon aurantiacus DSM 785 plasmid pHAU01, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
accagcccccgccaccgtcggagccgtg	Protospacer
. .**** *********.******** .

166. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP018064 (Rhodococcus sp. 2G plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
acgagccaccgccaccggcggagccgtg	Protospacer
.  ****.********* ******** .

167. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP030264 (Ensifer adhaerens strain Corn53 plasmid AB, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cattgccgccgccgccgccggagccccc	Protospacer
 .* *********.***********   

168. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagcgccgccgccaccgccgcggccggc	Protospacer
 .  **************** .***** 

169. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctccgccgccgccaccgcgggggccggc	Protospacer
  . ************** **.***** 

170. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP016619 (Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgaagccgccgccgccgccggagcgcat	Protospacer
 * **********.**********  . 

171. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP038031 (Rhodococcus ruber strain R1 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
acgagccaccgccaccggcggagccgtg	Protospacer
.  ****.********* ******** .

172. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
ctccgccgccgccaccgcgggggccggc	Protospacer
  . ************** **.***** 

173. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK977696 (Gordonia phage SCentae, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgaggccgccgccgccgccggagccccg	Protospacer
 * .*********.***********  .

174. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK977695 (Gordonia phage Pupper, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgaggccgccgccgccgccggagccccg	Protospacer
 * .*********.***********  .

175. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_015951 (Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
gcgtcgtgccgctaccgccggagccgga	Protospacer
*     .*****.***************

176. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP040720 (Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
acgagccaccgccaccggcggagccgtg	Protospacer
.  ****.********* ******** .

177. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP032678 (Pseudomonas sp. Leaf58 plasmid pBASL58, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tttagtcgccgccaccgccgcagccacc	Protospacer
  ***.************** ****.  

178. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP025436 (Gordonia sp. YC-JH1 plasmid pGOR1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
acgggccgccgcctccgccggcgccggc	Protospacer
.  .********* ******* ***** 

179. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP016821 (Rhodococcus sp. p52 plasmid pDF01, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
acgagccaccgccaccggcggagccgtg	Protospacer
.  ****.********* ******** .

180. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP047177 (Rathayibacter sp. VKM Ac-2759 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
atactccgccgccatcgccggagcggga	Protospacer
.    *********.********* ***

181. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KY883642 (Vibrio phage JSF15, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccgccgttgccgtt	Protospacer
 . *****************  ****  

182. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to KY883656 (Vibrio phage JSF9, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccgccgttgccgtt	Protospacer
 . *****************  ****  

183. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MN234183 (Mycobacterium phage Antsirabe, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccaccgccgccaccgccggcgccgat	Protospacer
 *. .**************** ****. 

184. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_022070 (Mycobacteriophage Wheeler, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cgccgccgccgccaccgccggcgccacc	Protospacer
 *. ***************** ***.  

185. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MF141540 (Mycobacterium phage Avocado, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
caccgccgccgccaccgccggcgcccgc	Protospacer
 .. ***************** *** * 

186. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK937593 (Mycobacterium phage Flypotenuse, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccaccagagccgcc	Protospacer
 . *************.**.******  

187. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH588544 (Caulobacter phage CcrBL10, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
tgatcccgccgccaccgcccgagccgcg	Protospacer
 *   ************** ****** .

188. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_026585 (Mycobacteriophage Estave1, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccgcctgcgccgcc	Protospacer
 . **************** * ****  

189. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MH536820 (Mycobacterium phage Glexan, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccaccagagccgcc	Protospacer
 . *************.**.******  

190. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MK801726 (Mycobacterium phage ChotaBhai, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagccgccgccaccaccagagccgcc	Protospacer
 . *************.**.******  

191. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to MG925349 (Mycobacterium phage Mendokysei, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
caccgccgccgccaccgccgccgccggg	Protospacer
 .. ****************  *****.

192. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NC_031109 (Gordonia phage Jumbo, complete genome) position: , mismatch: 7, identity: 0.75

ggtagccgccgccaccgccggagccgga	CRISPR spacer
cagagcctccgccaccgccggtgccgac	Protospacer
 . **** ************* ****. 

193. spacer 3.2|2068234|31|NZ_CP019798|CRT matches to NZ_CP033583 (Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence) position: , mismatch: 7, identity: 0.774

cgctgcccgagccggagccgcggtagccacc	CRISPR spacer
ggctgaccgagccggagctgcggtcggccct	Protospacer
 **** ************.***** * * *.

194. spacer 9.5|4885963|28|NZ_CP019798|CRT matches to NZ_AF135182 (Serratia entomophila strain A1MO2 plasmid pADAP, complete sequence) position: , mismatch: 7, identity: 0.75

cccctgggcggggttactgcgggtgccc	CRISPR spacer
ccccagggcggggtgactgcggggtagg	Protospacer
**** ********* ********     

195. spacer 9.5|4885963|28|NZ_CP019798|CRT matches to NC_002523 (Serratia entomophila plasmid pADAP, complete sequence) position: , mismatch: 7, identity: 0.75

cccctgggcggggttactgcgggtgccc	CRISPR spacer
ccccagggcggggtgactgcggggtagg	Protospacer
**** ********* ********     

196. spacer 1.4|1068386|36|NZ_CP019798|CRT matches to ASHF01000034 (Streptomyces sp. GBA 94-10 plasmid pGBA1, complete sequence, whole genome shotgun sequence) position: , mismatch: 8, identity: 0.778

ccggagggcgacttcgacggggtcggcgaacccgag	CRISPR spacer
ccggagcgcgacttcgacgcggtcggccaggtggtg	Protospacer
****** ************ ******* *. . * *

197. spacer 1.4|1068386|36|NZ_CP019798|CRT matches to NZ_CP011276 (Planctomyces sp. SH-PL62 plasmid pPL62-3, complete sequence) position: , mismatch: 8, identity: 0.778

ccggagggcgacttcgacggggtcggcgaacccgag	CRISPR spacer
gcggaggtcgacttcgtcggggtcggccaggtcgaa	Protospacer
 ****** ******** ********** *. .***.

198. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagcggccggagggcgtggccgaacccgat	Protospacer
*.  ..*********** * ********* 

199. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gcaccaccggagggcggcggcgaaccgatg	Protospacer
*    *********** ********* . *

200. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgagccggcgggcgtcggcgatcagcgc	Protospacer
*****.**** ************ *   . 

201. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP026091 (Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagcggccggagggcgtggccgaacccgat	Protospacer
*.  ..*********** * ********* 

202. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP046569 (Dietzia sp. DQ12-45-1b plasmid pII, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagaacatcgaggtcgtcggcgaacccgag	Protospacer
*. .*  . **** ****************

203. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP026093 (Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagcggccggagggcgtggccgaacccgat	Protospacer
*.  ..*********** * ********* 

204. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagcggccggagggcgtggccgaacccgat	Protospacer
*.  ..*********** * ********* 

205. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gcaccaccggagggcggcggcgaaccgatg	Protospacer
*    *********** ********* . *

206. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP021357 (Rhodococcus sp. S2-17 plasmid pRB11, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
gagaacatcgaggtcgtcggcgaacccgag	Protospacer
*. .*  . **** ****************

207. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ggcgaacaggatggcgtcggcgagatcacc	Protospacer
******* *** ***********. .*.  

208. spacer 1.6|1068488|30|NZ_CP019798|CRT matches to NZ_CP049042 (Pseudohalocynthiibacter aestuariivivens strain RR4-35 plasmid pRR4-35_5, complete sequence) position: , mismatch: 8, identity: 0.733

ttcgacggcgactgcgatcccgagtgcgtg	CRISPR spacer
ttcgaaggcgaccgcgatcccgaaaaccca	Protospacer
***** ******.**********. .* ..

209. spacer 1.6|1068488|30|NZ_CP019798|CRT matches to NZ_CP049142 (Pseudomonas nitroreducens strain HBP1 plasmid pPniHBP1_1, complete sequence) position: , mismatch: 8, identity: 0.733

ttcgacggcgactgcgatcccgagtgcgtg	CRISPR spacer
ttcgacggcgacttcgctcccgacaaggaa	Protospacer
************* ** ******  . * .

210. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 8, identity: 0.75

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
cgtcggtgccgcccgtgccggggggcggcgtc	Protospacer
 ***** ******* ***********     *

211. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP053565 (Pseudonocardia sp. Gen01 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
gctcggcgccgcccttgccggggcgctcaaca	Protospacer
* **** **************** **.*.   

212. spacer 3.1|2068186|28|NZ_CP019798|CRT matches to NZ_CP013071 (Sphingobium indicum B90A plasmid pSRL1, complete sequence) position: , mismatch: 8, identity: 0.714

ggtagccgccgccaccgccggagccgga	CRISPR spacer
accgcgcgccgccgccgccggagccggc	Protospacer
. ..  *******.************* 

213. spacer 3.2|2068234|31|NZ_CP019798|CRT matches to NZ_CP040819 (Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence) position: , mismatch: 8, identity: 0.742

cgctgcccgagccggagccgcggtagccacc	CRISPR spacer
ggctgcccgcgccggagccgcggcccggccc	Protospacer
 ******** *************.     **

214. spacer 3.2|2068234|31|NZ_CP019798|CRT matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 8, identity: 0.742

cgctgcccgagccggagccgcggtagccacc	CRISPR spacer
cgctgaccgagccggagctgcggacggcggt	Protospacer
***** ************.****  * *. .

215. spacer 1.4|1068386|36|NZ_CP019798|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 9, identity: 0.75

ccggagggcgacttcgacggggtcggcgaacccgag	CRISPR spacer
ccagtccccgacttccaaggggtcggcgaacccgga	Protospacer
**.*    ******* * ****************..

216. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK977708 (Mycobacterium phage Fulbright, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

217. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KU935731 (Mycobacterium phage Phrann, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

218. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MT498048 (Mycobacterium phage Raymond7, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

219. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MG099948 (Mycobacterium phage Philonius, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

220. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MH926055 (Mycobacterium phage Chewbacca, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

221. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524522 (Mycobacterium phage Purgamenstris, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

222. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MT723932 (Mycobacterium phage Schnauzer, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

223. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KU935726 (Mycobacterium phage Xerxes, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

224. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MT684588 (Mycobacterium phage Snekmaggedon, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

225. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MT498042 (Mycobacterium phage Rebel, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgacggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

226. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MT498044 (Mycobacterium phage Jamie19, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

227. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KU935730 (Mycobacterium phage Pipsqueaks, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

228. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KX756439 (Mycobacterium phage PhancyPhin, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

229. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MH316570 (Mycobacterium phage Silvafighter, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

230. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524518 (Mycobacterium phage Smurph, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

231. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK392367 (Mycobacterium phage BabeRuth, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

232. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524520 (Mycobacterium phage Nenae, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

233. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524515 (Mycobacterium phage Parmesanjohn, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

234. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MH697585 (Mycobacterium phage Gex, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

235. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KM588359 (Mycobacterium phage Carcharodon, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

236. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MH697576 (Mycobacterium phage Aggie, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

237. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MH697593 (Mycobacterium phage Tapioca, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

238. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to JN624851 (Mycobacterium phage Redi, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

239. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KU935727 (Mycobacterium phage Panchino, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgacggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

240. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to KU935729 (Mycobacterium phage SkinnyPete, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgacggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

241. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MG099936 (Mycobacterium phage Andies, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

242. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NC_031243 (Mycobacterium phage Xeno, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

243. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524509 (Mycobacterium phage SpongeBob, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

244. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to MK524528 (Mycobacterium phage ShrimpFriedEgg, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

245. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to JN256079 (Mycobacterium phage Charlie, complete genome) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
aacctctttgatggcgtcggcgaacccgag	Protospacer
..*   .. ** ******************

246. spacer 1.5|1068440|30|NZ_CP019798|CRT matches to NZ_CP024314 (Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence) position: , mismatch: 9, identity: 0.7

ggcgaaccggagggcgtcggcgaacccgag	CRISPR spacer
ctgatgccggagggcgacagcgaacccgaa	Protospacer
   . .********** *.**********.

247. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 9, identity: 0.719

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
cgtcggtgccgcccttgccggcggcggcaagc	Protospacer
 ***** ************** **   *. .*

248. spacer 2.1|1129052|32|NZ_CP019798|CRISPRCasFinder matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 9, identity: 0.719

ggtcggagccgcccttgccggggggcccgcac	CRISPR spacer
cgtcggtgccgcccttgccggcggcggcaagc	Protospacer
 ***** ************** **   *. .*

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	2062775 : 2068995	7	Bacillus_virus(16.67%)	NA	NA
DBSCAN-SWA_2	4647861 : 4705525	55	Moumouvirus(14.29%)	tail,tRNA,protease,plate	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP019798|2062775:2068995|DBSCAN-SWA
GATGGACGATCTGACACTGGTACGGGAGCACACGGTCTACCGGTGCGTGATGGGCTCCCGGGCGTTCGGGCTGGCCACGGAGGCCAGCGACACCGACCGGCGTGGTGTCTACCTCGCCCCGACACCGCTGTTCTGGCGGTTCGAGAAGCCCCCCACGCATGTGGACGGCCCGCGGGACGAGGAGTTCTCCTGGGAGCTGGAGCGTTTCTGCGAACTCGCCCTGCGGGCCAACCCGAACATCCTGGAGTGCCTGCACTCCCCCCTGGTGGAACACGTCAGTGCGGTCGGCGCGGAACTGCTCTCCCTGCGCGGGGCCTTCCTCTCCCGCCGGGCCCACACCAGCTTCGGCCGGTACGCGGCCTCCCAGCACGGCAAGCTCGTCGCGGACGTCCGCCTCCACGGAGCGCCGCGCTGGAAGCACGCCATGCACCTGCTGCGCCTGCTGCTGTCCTGCCGCGACCTGCTGCGCACCGGCCATCTGGCCATCGACGCGGGCCCTTACCGAGACCGCCTCCTCGCCGTCCGCCGCGGGGAGCTGACCTGGGACGAGGTCGACACCTGGATGACCCGGCTGCAGGAGGAGACGGAGGACGCCCTGGCCGGCACTCCCCTGCCGGAGGAGCCGGACCGGGCCCGGGTCGAGGACTTCCTCGTCCGCGCCCGGCGCGCGTCAGCCCTCCAGTGACGTCCGCCGGCGGACGACGTAGGCGTCCAGCATGGATCAGGCATCCCAGAGGGTGCCGAAGGCCAGGAGTTCGTCCCGGTACTCGATGCGGCCCTCCCACTCGCGCGGCCAGACGTCCGCCCCGAGGTGGGCTCCGGCGAAGGCGCCGGCGAGGCAGGCGAGGGAGTCGGAGTCGCCCCTGGTGCAGGCGGCGCGGCGCAGGGCGGTCAGGGGCTCGTCCGGGAAGAGCAGGAAGCACTGCAGGGCGGTGGCGAGGGCCTCCTCGGCGATCCAGCCGTCGCCGGTGGTCAGGCAGGGGTCGGTCTCGGGGGACGGGGTCTTCAGGGCGGCGGCGAGCCGGTCCAGCACCTCCAGGCACTCGTCCCAGCCGCGCGCGATGAAGGACTCCGGCGTGGCGTCGGAGGCGGTCCGCATCCACAGGTCGCCGAGCCAGCGCTCGTGGTAGCGGGTGCGGTTCTCCAGGGCGTACGAGCGCAGCCGCCCGACCAGGCCGGTGACCTCGGTGCCGGTGGCCAGCAGGTGGACCGCCAGCGCCGTCAGGTCGGAGGCGGCCAGGGCCGTCGGGTGGCCGTGGGTGAGGGCGGACTGGAGCTGGGCCGCGCCGGCCCGTTCCTCGTCGGTCCAGCCGGGGACCAGCCCGACGGGGACCACCCTCATGTTGGCCCCGCAGCCCTTGGAGCCGGTCTGGCTGGCGTCGCGCCAGTCGCGCTGCGGGTCGTTGAGCAGGTTGCAGGCCCGCAGGCAGGTGTTGCCGGGGGCCCGGTTGTTCTCCGGGGAGTGGTACCAGTCGACGAACTCCTCCCGGACCGGGCGGGTCAGGCGCAGCGGGCCTATGGGTCCGCGGTCGGTGGCGGTCCGGATGCCGCGGGCCAGGGCGAGGGTCATCTGGGTGTCGTCCGTGACGATCGCCGGGCGGGGCAGGCGCATCTCGCGCCACGGGCCGGTCTTGGCGAGGATCGCGGGGACGTCGTTGAACTCGGTCGGGAAGCCCAGTGCGTCGCCCAGGGCGAGGCCGACCAGCGCGCCCGTCGCGGCTCGTTTCGTCATGGGGTGGGTCCTTCCGGTCGGAGCAAAGGTGGATGGAGCGCGGTCGCCGGGCCGGCCCGGTAGAGGGCGGCCGGTTTGCCGCGGCCCCCGGTGAGCCGGGCGGCGCCCGGTACGGCCTCGACGAACCCGGGTGTCGTCAGGACCTTGCGGCGGAAGTTGGGACGGTCGAGCACGGTGTCCCAGACGGTCTCGTACACGGCCAGGAGCTCCCCGAGCGTGAACTCGGGCGGGCAGAAGGCGGTGGCCAGGCAGGTGTACTCCAGCTTCGAGCGGATCCTCATCCGTGCGTCCGCCAGGATCACCGCGTGGTCGAAGGCCAGGTCCGGGACCTCGCCCAGGGGCAGCCAGCGGGCCTGCGCCGCGTCCCCGCCGCCTTCGGCGGCCGGTTCGGGCAGGTCCGGGACGAGGGCCGTGAAGGCCACCGAGACGACCCGCATCCGGGGGTCGCGGTCCGGTTCGCTGTAGGTGCGCAACTGCTCCAGGTGCAGGGCCGCGACGACCTGCTCGGGCAGGCCGGTCTCCTCGGCCAGCTCGCGGCGGGCGGCGGTCTCGGCGGACTCCCGCGGCAGGACGAACCCGCCGGGCAGCGCCCAGGAGCCCGCGTACGGCTCCTGGCCGCGCCGGATCAGCAGCACGTGCAGGGCGCCGCCGCGCACGGTGAAGACGGCGAGGTCCACGGTCACCGCGAACGGCTCGAAGGCATGCGGGTCGTAGCCCGGGTCCACCGCCCCGCTCATCGGTTCTCCGGGAGGGGGTCGGCGAACCGCCAGCCTTCGGCGAGCAGTTCGTCCACGGCCGCCGCGGCCGTGGCGAGCCGCTCCCGGCGGTTGCCGCGTACGGAGAGGTAGCGCTTCCCGGTCGCCTCCAGTTCCTCGCGGAAGCGGCGGGTCATCCAGGGTCTGAGTTCGGGCCCGTCGCGCAGTCCGTCGTCCTCGAAGGGCACGTCGGCGTCCTCGGTCAGCAGGTACAGGTCCCGGTGGGTGAGGGCGGCGATCCGCTCGACCTCGGGGTTGCGGCCGCCCATGTACCGCTCGTGCCAGATGCCGGTGGCGAAGGAGTCGGTGTCGCAGACCAGCACCGGGGAGCCCTGGCGGGCCGCCCGCTCCTCCTCTTCGTCCTGGCGGCGGGCGATGACGGGGAACTCCTCCGAGGTGAAGGAGACGTCCGCCCAGGTGGCGGCCGGGTCGGCGGCCCGCGCCGCGGCGAGCTTCTCCTCGCTGTAGCGGCGGCCGTACTCCTCGACCCAGCCGGTGGCGGCCCAGACGCCGCCGCGCGCCCGCAGGTGCGCGGCCAGGTCCCGGGACAGGGTGGTCGTCCCGGTGGACTCGGCCCCCAGGACGACGACACGGCGCGCGAGGCGGGCCCGCACGGCCGGGCCGAGGAAGTCCCAGCAGGCGGCCGGGTCGGCCCGTACGGCGGTCCCGGAGACGGGGAAGAGGGTCCGGGCGGGGTCCACGCAGACCTCCTCGGCACCGAACCTGCGGGCGAGCTCGGTGCCGTACTCCTCGGAGGTGAAGACGGCGTCGACACGGCGGCCGACGGCGGCCCGGAAGATCGCCATGTGGGCCTCCCAGATCTCCGGGTCGTGCAGGTCGACGGGGATGTCGTCGACGGCTCCGACGACGTCCGCGTCCGGGTGGGCCTCGCGCATCCAGGCGACGCGGTCGGCGAGCGGCACCGATTCCACGGAGGCGGCGCAGACCAGGACGGTCAGCCTCTCGCAGCGGTCCTGGGCGGTGCGCACCAGGTGGTGGTGGCCGGCGTGCGGCGGGTAGAACTTGCCGAGCACCAGCCCGTGGCCGAAGCGCCTCATGCCGTCGCCTCCAGGGCGGTACGGGCGCCGCGCTGCGGGAGCGAGCGCCGCCAGCCGAGCAGGCCTGCGACGCAGAGGGCGAGGAATCCGACGTAGAGCAGGGCGGTGAGGTGGAGCCCCTTGTGGACGTACAGGGGGATGTAGAGGAGGTCGGCGGCGATCCACAGCCACCAGGACTCGACCAGCTTGCGGCACTGGCCGTAGGTCGCCGCGAGGGAGAGCGCCGTCGTGGCCGCGTCCCAGACGGGGACGGTGGAGTCGGTGGCGCGGGCGAGGAGCAGGGTCAGGCCGAGGGTCCCCGCCGCCCCCGCCGCGGCGAGCCAGACCCATTCGGTGCGCGTGGTGCGGCGCACCGGCAGGGCTGCGGCGGTTCCTGGTCCACCCCCGTGGGTCCAGGACCACCAGCCGTACGCGGCGAGGGCGATGAAGACGATCTGGAGCCCGGCGTCGGCGTAGAGGCCGGCCTGGGCGAAGAGCACGATGAAGAAGACGTTGTTGGCGATGCCGATCGGCCAGTTGGCGATGTGCTGCCGGGCCACCAGCCAGACGCACAGGGCGCCCGTGGCGAACCCGAGCACCTCGGTCCAGCTCAAGGTCCAGTTCATGCCCGACCCGCCTTCCTTTAATAGTCACTGTGACTATAAACAGGAGTGCGGGGCTCGGGCAAGGGAGAAGCCCGCAGTGCCGTGGGCACTGCGGGCTTCTCGTGGAGCGGGGTCGGGCGGAGGGCCTACAGGCCGACCTCGCGCATCAGCATGCCGACCTCGGTGTTGGTCAGGCGGCGCAGCCAGCCGGACTTCTGGTCGCCCAGCTCGATCGGGCCGAAGGAGGTCCGGACGAGCTTGTCGACGGGGAAGCCCGCCTCGGACAGCATGCGGCGCACGATGTGCTTGCGGCCCTCGTGGAGGGTCACCTCGACCATGTAGTTCTTGCCGACCTGGTCCAGGACGCGGAAGTTGTCGGCGCGGGCCCAGCCGTCCTCGAGCTCGATGCCGTCCTTGAGGCGCTTGCCGATGTCGCGCGGCAGCGAGCCGGTGATCGCGGCGACGTAGGTCTTCTTCACGCCGTACTTCGGGTGCGTCAGGCGGTGGGCCAGCTCACCGTGGTTGGTGAGCAGGATGATGCCCTCGGTCTCGGTGTCCAGCCTGCCGACGTGGAAGAGGCGCGTCTCGCGGTTGTTGACGTAGTCGCCCAGGCACTGGCGGCCGTCCGGGTCCTCCATGGTGGAGACGACACCGGCCGGCTTGTTCAGCGCGAAGAACAGGTACGACTGGGTGGCGACGGTCAGGCCGTCCACCTTGATCTCGTCCTTCGGCTGGACGCGCTTGCCCTGCTCGGTGACGATCTCGCCGTTGACCTCGACGCGGGCCTGCTCGATGAGCTCCTCGCAGGCGCGGCGCGAGCCCATGCCGGCGCGGGCGAGGACCTTCTGCAGCCGCTCACCCTCCTGCTCGGCCCCGGGGAAGGTCTTCGGAGTCTTGATCACGGGCTTGTCGGCGTACCGGTCGCGCACGCGCTCCTCGATGCGCGCGTCCAGCTCGCGCGGGCGGGACTGGCCGCTGCGGCTGCCCGGACCGCGGCGCGGGCCGCCGGCGCCGCCGATGCCGGGGGTCTTGGAGGCCTTGGGGCTGCCCTTGGCACCACCGCGCGCGGCCGCACCGCGGGCGCCGCGGGTGCGCTCACCCTCGGGGCCCACGTCGTAGCGGCGCTCCTCGGGGCGCGGGTTGCGGGGGCGCTGCGGAGCCTGGTCGCGGTCACGGTCCCGCGAGCCGCCCTGGCCGCCCTGGCCGCCCTGGCCGCCCTGGCCGCCCTGGCCGCCGCGGTAGCCGCCGCCACCGCTGCCCGAGCCGCCGCCGGCACCGCCCCGGTAGCCGCCGCCACCGCCGGAGCCGGAGCCGCCGCGGTAGCCGCCGCCGCTGCCCGAGCCGGAGCCGCGGTAGCCACCGCCGCCGCCGGAGCCGCCGCCACGGGCGCTACCGCGCCCGCCGCCGCCGGAGCCGCCGCTGTTCCTGTTGCCACCGTTGCCGTTGCCGCTGCTTCGCATCAAAGTTCCGTCGTCTTGTCGTCTTCATCGGTGTCCGGTGCGTCCGGATCGAACGACGGCACACCTTCTTGCGTCTCGGCTTCGATCGCGTCCGCCTCGGGGAGGAAGGGCGCGAGCTCCGGGAGCTCGTCCAGGCCGCGCAGGCCCATCCGCTCCAGAAAGTAGTTCGTCGTCCTGTATAGGATCGCACCTGTTTCGGGTTCCGTCCCCGCCTCCTCCACCAGACCGCGCTGGAGGAGGGTCCGCATGACCCCGTCGCAGTTGACTCCGCGCACGGCGGAGACCCGCGACCGGCTCACCGGCTGGCGGTACGCGACGACCGCCAGGGTCTCCAGCGCCGCCTGCGTCAGCCGGGCCTGCTGGCCGTCCAGGACGAAAGCCTCGACGGCCGGGGCGTACTGCGCGCGGGTGTAGAACCGCCACCCGCCCGCGACGAGCCGCAGCTCGAAGCCCCTGCGCGCGGCCGTGTACTCGTCGGCGAGCTCCCGCAGCGCGTCCGCCACCTCGCGCGGGGTGCGCTCCAGCACCTTGGCGAGGTGCGCCTCGGTCGCGGGCTCGTCCACGACCATCAGGACGGCCTCCAGGGCCGGCTTCAGTTCCAGTGCGGCCACCGCGCCGCCGTCGCCGCTCAA

Protein sequences of DBSCAN-SWA_1

>NZ_CP019798|2062775:2068995|2062775_2063459_+|WP_030855312.1|DBSCAN-SWA
MDDLTLVREHTVYRCVMGSRAFGLATEASDTDRRGVYLAPTPLFWRFEKPPTHVDGPRDEEFSWELERFCELALRANPNILECLHSPLVEHVSAVGAELLSLRGAFLSRRAHTSFGRYAASQHGKLVADVRLHGAPRWKHAMHLLRLLLSCRDLLRTGHLAIDAGPYRDRLLAVRRGELTWDEVDTWMTRLQEETEDALAGTPLPEEPDRARVEDFLVRARRASALQ
>NZ_CP019798|2062775:2068995|2067049_2068363_-|WP_078093951.1|DBSCAN-SWA
MRSSGNGNGGNRNSGGSGGGGRGSARGGGSGGGGGYRGSGSGSGGGYRGGSGSGGGGGYRGGAGGGSGSGGGGYRGGQGGQGGQGGQGGQGGSRDRDRDQAPQRPRNPRPEERRYDVGPEGERTRGARGAAARGGAKGSPKASKTPGIGGAGGPRRGPGSRSGQSRPRELDARIEERVRDRYADKPVIKTPKTFPGAEQEGERLQKVLARAGMGSRRACEELIEQARVEVNGEIVTEQGKRVQPKDEIKVDGLTVATQSYLFFALNKPAGVVSTMEDPDGRQCLGDYVNNRETRLFHVGRLDTETEGIILLTNHGELAHRLTHPKYGVKKTYVAAITGSLPRDIGKRLKDGIELEDGWARADNFRVLDQVGKNYMVEVTLHEGRKHIVRRMLSEAGFPVDKLVRTSFGPIELGDQKSGWLRRLTNTEVGMLMREVGL
>NZ_CP019798|2062775:2068995|2065239_2066319_-|WP_060179957.1|DBSCAN-SWA
MRRFGHGLVLGKFYPPHAGHHHLVRTAQDRCERLTVLVCAASVESVPLADRVAWMREAHPDADVVGAVDDIPVDLHDPEIWEAHMAIFRAAVGRRVDAVFTSEEYGTELARRFGAEEVCVDPARTLFPVSGTAVRADPAACWDFLGPAVRARLARRVVVLGAESTGTTTLSRDLAAHLRARGGVWAATGWVEEYGRRYSEEKLAAARAADPAATWADVSFTSEEFPVIARRQDEEEERAARQGSPVLVCDTDSFATGIWHERYMGGRNPEVERIAALTHRDLYLLTEDADVPFEDDGLRDGPELRPWMTRRFREELEATGKRYLSVRGNRRERLATAAAAVDELLAEGWRFADPLPENR
>NZ_CP019798|2062775:2068995|2066315_2066924_-|WP_060179956.1|DBSCAN-SWA
MNWTLSWTEVLGFATGALCVWLVARQHIANWPIGIANNVFFIVLFAQAGLYADAGLQIVFIALAAYGWWSWTHGGGPGTAAALPVRRTTRTEWVWLAAAGAAGTLGLTLLLARATDSTVPVWDAATTALSLAATYGQCRKLVESWWLWIAADLLYIPLYVHKGLHLTALLYVGFLALCVAGLLGWRRSLPQRGARTALEATA
>NZ_CP019798|2062775:2068995|2068362_2068995_-|WP_030855320.1|DBSCAN-SWA
MSGDGGAVAALELKPALEAVLMVVDEPATEAHLAKVLERTPREVADALRELADEYTAARRGFELRLVAGGWRFYTRAQYAPAVEAFVLDGQQARLTQAALETLAVVAYRQPVSRSRVSAVRGVNCDGVMRTLLQRGLVEEAGTEPETGAILYRTTNYFLERMGLRGLDELPELAPFLPEADAIEAETQEGVPSFDPDAPDTDEDDKTTEL
>NZ_CP019798|2062775:2068995|2063495_2064506_-|WP_078093949.1|DBSCAN-SWA
MTKRAATGALVGLALGDALGFPTEFNDVPAILAKTGPWREMRLPRPAIVTDDTQMTLALARGIRTATDRGPIGPLRLTRPVREEFVDWYHSPENNRAPGNTCLRACNLLNDPQRDWRDASQTGSKGCGANMRVVPVGLVPGWTDEERAGAAQLQSALTHGHPTALAASDLTALAVHLLATGTEVTGLVGRLRSYALENRTRYHERWLGDLWMRTASDATPESFIARGWDECLEVLDRLAAALKTPSPETDPCLTTGDGWIAEEALATALQCFLLFPDEPLTALRRAACTRGDSDSLACLAGAFAGAHLGADVWPREWEGRIEYRDELLAFGTLWDA
>NZ_CP019798|2062775:2068995|2064502_2065243_-|WP_060179958.1|DBSCAN-SWA
MSGAVDPGYDPHAFEPFAVTVDLAVFTVRGGALHVLLIRRGQEPYAGSWALPGGFVLPRESAETAARRELAEETGLPEQVVAALHLEQLRTYSEPDRDPRMRVVSVAFTALVPDLPEPAAEGGGDAAQARWLPLGEVPDLAFDHAVILADARMRIRSKLEYTCLATAFCPPEFTLGELLAVYETVWDTVLDRPNFRRKVLTTPGFVEAVPGAARLTGGRGKPAALYRAGPATALHPPLLRPEGPTP

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_030855312.1|2062775_2063459_+	nucleotidyltransferase domain-containing protein	G3M9V9	Bacillus_virus	1.1e-13	29.5
WP_078093949.1|2063495_2064506_-	ADP-ribosylglycohydrolase family protein	A0A2D0ZND4	Rhodococcus_phage	1.5e-30	32.3
WP_060179958.1|2064502_2065243_-	NUDIX hydrolase	A0A1W6DX89	Sphingobium_phage	7.5e-11	40.0
WP_060179957.1|2065239_2066319_-	AAA family ATPase	A0A2K8HHU5	Bacteriophage	4.3e-31	32.4
WP_060179956.1|2066315_2066924_-	nicotinamide mononucleotide transporter	A0A0F6YPU8	Sinorhizobium_phage	3.6e-11	30.7
WP_078093951.1|2067049_2068363_-	rRNA pseudouridine synthase	NA	NA	NA	NA
WP_030855320.1|2068362_2068995_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	1.9e-10	29.9

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP019798|4647861:4705525|DBSCAN-SWA
GTCAGAGCTTCTCGGGGGTGCGGATGCCCAGGAGGGACATGCCCTTCGAGAGGGTGCGGGCCGTCAGCTCGCACAGGAACAGACGGTTCTCGACCTGCTCCGCCGTGTCCGCCTTGAGGACCGGGCACTCCGAGTAGAACGACGTGTACAGCGACGCCAGCTGGTACAGGTACGCCGCCAGCTTGTGCGGGGCGTGCTCCGCGGCCGCCTCCGCGATCAGCTCGCCGAAACCGTCCAGGTGCAGGCCCAGCGCACGCTCGGTCGGAGCGAGCGCCACCTCCGGGTGGGCGGCCGGCTTCGCGTCGCCCGCCTTGCGCAGGATCGACTGGATACGGGCGTACGCGTACTGGAGGTACACGGACGTGTCGCCGTTCAGCGAGACCATCTGGTCCAGGTCGAACTTGTAGTCCCGGGCGGCGGACGTCGACAGGTCGGCGTACTTCACCGCGCCGATGCCGACCTGGGCACCCCGCTCGGCGATCTCGGCCTCCGTCAGGTCCTGGGCCTTCTCGCGGACCACCGCCGAGGCCCGGTCGATCGCCTCGTCCAGCAGGTCCACCAGCCGGACCGTCTCGCCCTCACGGGTCTTGAACGGCTTGCCGTCCTTGCCGAGGACGGTGCCGAAAGCCAGCTGTACGGCCTTGACGTCGTCGTTCAGCCAGCCCGCCCGGCGCGCCGTCTCGAAGACCATCTTGAAGTGCAGCGACTGCCGCGCGTCGACCACGTAGATCAGCTCGGTCGCGCCGAGGTTGCCCACCCGGTCCCGGATCGCCGACAGGTCGGTGGCCGCGTAGCCGAAGCCGCCGTCCGACTTCTGCACGATCAGCGGGGTCGGGTTGCCGTCCGGGCCCTTGACGTCCTCGAAGAACACGCACAGCGCACCGTTGGAGCGGACCGCGACGCCCGACTCCTCCAGCAGCTTGCACGTCTCGACCAGCATGTCGTTGTAGCCGGACTCGCCGACCACGTCCGGGTCCCGGATGTCCATGTCCAGCTTGTGGAAGACGGAGTAGAAGTAGATCTTCGACTCGTCCACGAACCGCTGCCACAGCGCCAGCGTCTCCGGCTCGCCCGCCTGGAGGTCCACCACCCGCGCCCGGGCCCGCGTCTTGAACTCCTCGTCGGAGTCGAAGAGGGCGCGCGAGGCCTTGTAGAGGCGGTTGAGGTTGGACATGGCCTCCTCGCCGGAGGCCTGCTCGTCGCCGTCGCCGGACCTGTGGTCCAGCTCGTGCGGGTGCTCCAGCAGGTACTGGATGAGCATGCCGAACTGGGTGCCCCAGTCGCCGATGTGGTGGCGCCGGATCACCTTCTCGCCCGTGAACTCCAGGATCTCCACCATCGCCGCGCCGATCACGGCGGACCGCAGGTGCCCGACGTGCATCTCCTTGGCGACGTTCGGCTGCGCGTAGTCGATCACCGTCGTGCCGGCGGACGCGTTCAGCGGCACGCCGAGCCGGTCGTCCGCGGCACGCGCCGCCAGCGTCGAGATGATCGCCCCGTCGGCGACGGTGATGTTCAGGAAGCCGGGGCCGGAGACCTCGATCTCCTTGATCAGGTCACCGGTCGGGATGCCCCCGACCACGGTCGTGGCCAGCTCGCGCGGGTTGGCCTTGGCCTTCTTCGCGAGTGCCAGGATGCCGTTGGCCTGGAAGTCGGCCCGGTCGCTACGTCGCAGCAGCGGGTCGGCGCCACCGGCCTCCGGCAGCGCGGAGGCGAGGGCGTCGGCGACGCGCTGGTTGACGGACGAAGCGAGCGAAGGGACCGAGGCCATGAGCTGCCGTTCCTGTGAGTCTGGTACCGGGGTCGGACTTGGGTCTTGCGACAAGTGCCGAGTATCCCACGAGGGCGCCATCCGTTTCGCGGGATATCACCGGGTGGAAGCAACCCCGGAGTGGCCCGTTCCGTCTGGGAGAATGGCCGAAGCCATCATTCGAGATAGAAGGACGTGTCGTGGCTCAGAGCGCGCAGAGCAGCACCGAGACCGACTGGGTCTCCCGTTTCGCGGACGAGGTCATCGCCGAGGCGGAGCGCCGAGCCCCGGGCAAAGCGGTCGTCGTCGCGTCCGGACTCTCCCCCTCCGGCCCGGTCCACCTCGGCAACCTCCGCGAGGTCATGACCCCGCACCTGGTCGCCGACGAGATCCGCCGCCGCGGCCACGAGGTCCGCCACCTCATCTCCTGGGACGACTACGACCGCTTCCGCAAGGTCCCCAAGGGCATCCCCGGCGTCACCGAGGAGTCGCACGCCCAGCACATCGGGCGCCCGCTGACCGCCGTCCCCGCCCCCGAGGGCTCCGCGTACCCGAACTGGGCCGAGCACTTCAAGGCCGCCATGGCCGAGTCCCTGGCCGAGCTCGGCGTCGAGTACGACCCGATCAGCCAGACCGAGCAGTACACCACCGGCGTCTACCGCGAGCAGATCCTGCACGCGATGAAGCACCGCGGCGACATCGACGCCGTCCTCGCGCAGTACCGCACCAAGGTCAAGCCCGGTGGCAAGAAGCCCCAGCAGAAGCAGGTCGACGAGGCCGAGCTGGAGGCCGCCGAGGGCTCCGGCGCGGCCGCCGAGGACGACGGCAGCGCCGGCGAGGGCGGGTACTTCCCGTACAAGCCGTACTGCGGCCGGTGCGGCAAGGACTTCACCAAGGTCACCTCGTACGACGACGAGACGACCGAGATGACCTACGTCTGCACCGAGGACGACTTCACCGAAACGGTCAAGCTCAGCGAGTTCAACCGCGGCAAGCTCGTCTGGAAGGTCGACTGGCCGATGCGCTGGGCCTTCGAGGGCGTGATCTTCGAGCCCTCCGGCGTCGACCACTCCTCGCCCGGCTCCTCCTTCCAGGTCGGCGGCCAGATCGTCCACATCTTCGGCGGCGAGCAGCCCATCGGCCCGATGTACGCCTTCGTCGGCATCAGCGGCATGGCCAAGATGTCCTCCAGCAAGGGCGGGGTCTTCACCCCCGGCGACGCCCTGCAGATCATGGAGCCGCAGCTCCTGCGCTGGCTCTATGCCCGCCGCCGGCCCAACCAGTCCTTCAAGATCGCCTTCGACCAGGAGATCCAGCGCCTGTACGACGAGTGGGACAAGCTGGAGGGCAAGGTCGCGGACGGCAGCGTGCTGCCCGCCGACGCCGCCGCCCATGCCCGCGCCGTACGCGTCGCCTCCCACGAGCTGCCGCGCACCCCGCGCCCGATGCCCTACCGCACCCTCGCGTCGGTCGTCGACATCACCGCCGGGCACGACGAGCAGACCCTGCGCATCCTCTCCGACCTGGAGCCGGACAAGCCGCTCACCTCCCTCGACGAGGTACGGCCGCGCCTGGACCGCGCCGAGAACTGGATCACCACCCAGGTCCCGGCCGACCAGCGCACCCTCGTACGCGAGGACGCCGACACCGAGCTGCTCTCCTCCCTGGACGACGAGGGCCGCGAATCGCTGCGCCTGCTCCTGGACGGCCTCGACTCGCACTGGTCGCTCGACGGGCTCACCACGCTCGTCTACGGCGTCCCGAAGGTCATGGCAGGACTGGAGCCCGACGCCAAGCCGACCCCCGAGCTCAAGGTCGCGCAGCGCACCTTCTTCGCCCTGCTCTACCGGCTCCTCGTGACCCGGGAGACCGGGCCGCGCCTGCCCACGCTGCTGCTGGCGGTGGGCGCGGACCGCGTGCGCAAGCTGCTCGCCGTCTGAGACCCGGCCCCGGGCCGTGCCCGGGCATGCGGAAGGGCCCGCACCCCTCGGGGTGCGGGCCCTTCCGCATACAGCTGCCTGCCTGTATGTCTGCCTGTCTGCCTGCCCGCTACGCCGGCTCGGCCTCCCGGTCCTTGTGGTGCTGCTGCCGGAACGACGAGATCATCCGCCGCAGGAGCGAACCACTGCGCGGGTGCGTCACGCCATAACGGTCCGCCAGCACTATGTCGAGGGCCTCGGCGGTCGGATAGTCCTGCGTCTCCTCGGCCAGCGAGCAGAACACCTTGTACGCGATCTGCGCGAACTCGACCTCGTCCGGGGAGTCCACCTCCGGCACCTGCTCCGGGAAGTCCCCGTCCGGAGCCCCCTCGTGACGCGGCTCCGGAACCGGGAGCTGCTGCGCCTGCTGGTCGTCCGGGCCCATCGGGGGCAGCACCGGCGTCGGTTCCAGGCCCTCGACGTACTGCGGGTTGTAGCCGCCCTCGTACGCCGCCTGCGGCGCCTTCGGCGCGGCGAACCAGGCGCTGTTGTGGGCCGCGGGCATCGCCGTCGGGTCCACCGCGAACGCCGGCGGGGCGTGGGGGGTGGCCGGCGCGGGCGCCACCTGCTGGACCTGGGCCGAGAGCTGCTGGGGCTGGGCCTGGTCAGCCTGTTGGGACTGCTGGGACTGCCGGGCCGGATCGTCCCATTCCGGGGCGCCCGCCGCCGCGCCAGCCACTGCGCCCGTCGCCGGGGCCTCCAGGGCCGGAGCCGTCCCCGCGACCTGCTGCTCCAGCGGAGGCAGCACCGCCGGATCGATCCCGGTCGCGGCCAGCGCGTCCGGCGTCGTCTGCGACAGCGGGACGCCGATCCGGGCCAGCTTCAGCGGCATCAGCGCCTCCACCGGCGCCTTCTGCCGCCAGAAACGCCCGTACCGTGCCTGAAGGCGCGCCTGGTAGATCAGCCGGTCCTGCTCCATGCCGATCGCCTGCTCGTACGAGCGCAGCTCCCACAGCTTCATACGGCGCCACAGCTTGAACGTCGGCACCGGCGACAGCAGCCACCGTGTGATGCGCACGCCCTCCATGTGCCGGTCCGCCGTGATGTCGGCGATCCGGCCCACCGCGTGCCGGGCGGCCTCGACCGTCACCACGAACAGGATCGGGATCACGGCGTGCATGCCGACACCGAGCGGATCCGGCCACGACGCCGCGCCGTTGAACGCGATGGTCGCCGCCGTCAGCAGCCACGCCGTCTGGCGCAGCAGGGGGAAGGGGATCCGCATCCAGGTCAGCAGCAGGTCCAGCGCCAGGAGCACGCAGATACCGGCGTCGATGCCTATCGGGAACACCAGGGAGAAGCTGCCGAAGCCCTTCTTCTCCGCGAGTTCGCGCACCGCGGAGTACGAGCCCGCGAAGCCGATGCCCGCGATGACGACGGCTCCGGCGACGACGACACCGATGAGTATTCGGTGCGTACGAGTCAGCTGCATCGCGGCCACCCGCGATCCCCTCCCCTTGTCGAGCACAAACCGAGCGCTTACCGCGCCTTTACGGAGCTGCGGCAGGCACAGCGTACGGGTGACCGGAAGTCAGCGCTCCAGGAGGCCCCGACGCGCCGCCGTCCTACTGGGGCTGGGGGGACTGCGGCTGCTGCTCCGCCGGCTTGTTGGCTCCCGCGACCGAGGCCACGGCCTCCTTCGCCGCGGTGATCGCGTCCTGGAGCAGCTTCGCCTGGTCCGGGGCGCCTGCACCCTCGTAGGCGGCACCGTTGTAGTCGAGCGTGACGACCACGTTCTGGGTGCGCGCCACGATCGTCGTGTTGAAGAAGTCGACGTCCTTCTTCACCGAGTACACGATCGAGGTGCCCTGGTCGCCCAGGCCCTCCACGGCCTCGGCCTTCACGTTCTGCGCGCCCTCGGAGGCCTTCGCCGACTCGACCTGCTTGCCGTACTGCTCCTCGGCACGCTTGTTGGCGCCGCCGAGCGAGGCGTGCGAATCGGTGCGGAAGTAGGAGAGCGAAAGCCAGCGGTACTGCGAGCCCTTCAGGCCGTCCTCGTCCAGACCGTTCCAGGAGCAGCTGGCCCGGGTGGCCAGGTCGTTCGACTTGGTCGCCGTGCCGTTCTTGTCCTTGGCCTCGGGGACGAGCGTGTCTATCGTGCCCGCCTGTATCGCCTTGCAGGGGTCCGGGAGGGTGGCGAAGGCGGCCTTCTCCAGCTCCGGCTTGGACTTCTTCTCGCCGGGCTTCGCGGAAGCGGACGAACCGGACTTCTTGTCGCCCTTGTCGGCGGACTCCTTGCCCGAGTCGGAGGAACACCCGGCCACGGTGAGGATCACCGGGACGGCTGCGCAGGCGAGAACGCGGGTGAGGCGCGAGGCTGATCGGTGCATGGTTCCTTCAGTGCTTCGGGGATCGTCTTCGGACGCGGGACCCGGTCAACGGTAGCCCGATCGGGTGCCGCACTGCTGTGCGCGCCGTCACGCCGGGGCGTGTCGCGCACCGCTCACTCGTTGAGGCGTTCGGCGAGAGCCTGCGCCAACTGCCGTGCCTTGTCCTGGGTTTCACCGCTCGGCGGGATGGTTCCGGGCAGCGTCGGCTGCACGCTGTACTCGATCTTGACGATGACATTCGAGGTACGGAACACAATCCGGACGGTGCGCGACTGGGCCGCCGTGGCCCCGGCGGCGCTCAGCTTGTCGTCCAGGAACGCCTCGGTGCCGAGCCCCTCCAGGACGCGGGAGCCGAGCTCGGGCTGGGCGGACGGGCTGGTGCCGGGTGCGGGCGTCCCCGCGGCCGGCGCCCCGGCCGACGGCGCGCCGCTCGCGGGCGGTGCGGCGGGCGGTGCGGCGGGCGGGGGCGTGGAGGCGGCGGGGTTGGCCGGGTTGGCCGGGTTGCCCGGGTTGGCGGCGCCCGGGCCGGGGGTGGTGACGGGGCCGGGGAAGGGCAGGTGCGCGTCGGTGAGCAGGCGTACGTAGACCTGCTTCGCCTTGTCGTCGTCGCTGGCGGCGCCACGGTCGTAGGAGACCACGCGCTCGAAGCCGACCGACAGCAGCCGGGTCTCCTCGGGGGTCTGGGCGGTCCAGCGGCAGCCGACGTGCCGGTCGCCGTCGTACGAGGCGTCGGCGACCCCCGCGTACAGCTGGTCGCGCTGCTGGGGGGTGAGGCTGTCCGGCGCGGGGAGCATGGCCTTGAGCTTCTTGCTGTCGGCGGCCGCCCGGCAGGGCGCGGGCAGGCTGCGGTACTTCCCCGGCTGGGCGGGCGCGGCGGAGCTGCCGCCGGCCTTCGAGTCGCTGGTGCTTCCCCCGTCGCTCCCGCCGGTGCACCCGGTCAGGCCGGCCGCGCCGGCCGCGAGCGCGGTGAGCATCGCGATGCCGGGCAGGACTCGCCGTACCGCTTTGCGCTGCACGTCCACTGGCTCCCTTCGACCGGCGGGCCCCCCGACGGTCAGGAAAATGCGTTGCCGCGACTTGGGCGCGGCTGGACACAATGTCTATCGCACACGCTGGTGCTGGCGCCGGTCCCCTGTCGTATTTGGGATCAAGAGCGAGGCTTTTGCGCATTCTCACCTTTCTGTTGTTTTCAGGGGATTGATCCTTATGTCGTATGTAGAGGTACCGGGGGCACAGGTCCCGATCCGGATGTGGACCGACCCCGCGTCGGTCGAGGCGGGAGCGATGCAGCAGCTCCACAACGTCGCCACCCTTCCGTGGATCAAGGGCCTGGCGGTGATGCCGGACGTCCACTACGGCAAGGGGGCCACGGTCGGCTCGGTGATCGCCATGAAGGACGCGGTCTGCCCGGCGGCGGTGGGTGTGGACATCGGCTGCGGCATGTCGGCGGTGAAGACGTCCCTGACGGCGAACGACCTCCCGGGCGACCTCTCCAAGCTCCGCTCGAAGATCGAGCAGGTGATTCCGGTGGGGAACGCGATGCACCGGGAGGCGGTGGACCCGTCGCGCCTGTACGGATTCACCGAGGCGGGCTTCGGGGACTTGTGGGAGCGCTTCGACTACGTCGCGGATGCCGTGAAGTTCCGGCGGGATCGCGCGATGCGGCAAATGGGAAGCCTTGGCCAAGGAAATCACTTCTGTGAAGTCTGTATCGATTCATCAGGTTCGGTGTGGCTCATGCTGCACTCGGGCTCGAGGAACATCGGCAACGAGCTGGCTGCCTTCCACATTGGCGTTGCGCGCGGACTCTCCCACAATCAGAACCTCGTCGACCGGGACCTGGCGGTCTTCCTCGCCGCCACGCCGGAGATGGAGGCGTACCGCAACGACCTCTTCTGGGCGCAGGAGTACGCCAAGTACAACCGGGCCGTGATGATGAGCCTCTTCAAGGAGGTTGTCCGCAAGGAGTTCCGCAAGGCCAAGGTCTCCTTCGACCGCGAGATCAGCTGCCACCACAACTACGTGGCGGAGGAGCGGTACGACGGCATGGACCTGCTGGTCACCCGCAAGGGGGCGATCCGCGCCGGCAGCGGTGACTACGGGATCATCCCGGGCTCCATGGGTACGGGTTCGTACATCGTGAAGGGCCTCGGCAACGAGAAGTCATTCAACTCGGCCTCGCACGGCGCGGGCCGGAAGATGAGCCGGACGGCGGCGAAGAAGAAGTTCTCGGCGCGCGACCTGGCGGAGCAGACGAGGGGCGTGGAGTGCCGTAAGGACTCGGGCGTCGTGGATGAGATCCCCGGCGCGTACAAGTCGATCGAGCACGTCATCGACCAGCAGACCGACCTCGTCCAGGTCGTGGCGAAGCTCAAGCAGGTCATCTGCATCAAGGGCTGAGGCTGCCCGGGCGCGGTCGGGGGAGTGGAGGGGCCCGGACCGATCGCGATCGGTCCGGGCCCCTCCACGTTGTCTCGTCAGGCTTTACCGGTGCGCAGCCGCCAGAGGCGCATGGAACAACTCTGCGCGGTCCTGTCGAGGGCGATTCCGGCTGCTGCGGGGTCGTTCAACCGCAGGAGGGTCTCGTCATCCTTTGGGGTCCAACGGCGGCGGGGTGGAGCGACCCGCATGTCTGCAGGTCGGACCCAGTTGAGGAGTTCTGCAGCCCTGGCCTTCTTGCGCCCCAGGCCCAGGCAGCCCTCGTAGTACAGGTGCGCGGCCAGGGCCTGGGCAGCCTCCTTGGTGTAGAGGATGTTGTAGATGCCGTCTCGCGTATTGCGCTTGATGGTTCGCTCCGCCCCCGTGATCTTCTTGGCGTAGTGGCACAGGTAGGCGCCTAGTGCCGTGCTCGCGGTGGTGAGCGAGACGAACGGCAGGCCCGTGTTCGTGTAGCCGACGGAACCGTCGGCGTCGATGACTCCCCGAAGGTAGTCGCGACGTGAGAAGTCCACGCGGGGAGGCCTGATGTTCATGGACTTGGGTCCGTAGGGGAGCCCCAGTTCGTTGATTGCGCTCCGTGCTTCGAGGGAGCAGAGGCTCCAGGTGGCTGAGGTGTGGGACTCGGAGAAGTTGGTCGCCCGGGTGCGCTCGGAGATGGAGCTGTAGTAGGGCGTGAGGCGTTGGAACTCGCGAAGGATCTCGATGTCCCGTGCGTTGACCTCCGCCGTGAGCTTGCCCTTCTGGCCGCTGCCTTGGGCGAGGTGCCCGTCGGCCTGCAGGAAGCCGAACATATAGGCGTAGCGGGGGTCTTGGAGGTCCATGAAGCGTCCAGGGGCGCTAGGGTCCTGGTCAGCCATGAGGAAGCCTTTCTTCCTTGCCGGTGAGGCCCTCGGTCGGGACTGCCATCCCGGGCGGGGGCCGTTTGTGTTGTGGCTGAACCTAGGTGCGGGTCGGCTGGGCGGGGCGCCGAACGGGCGCGGTTCACTCGAACGTATGGCGGAATGTCGAGGTCCGGAAAGGGGCGGCTCCCGGTCTCGCGGAGAAGCCGTCACGAGTCTGAACTTTCCTTTGGTGCAGGGGGAGTTGACCGCGGTGTTGGTCTGACCAGGGTGGCGGTATGGGGGAATCCGCGTGCTTGTCGCCGTGTTCGCGGCGTCGTCGCTGGCTTTAGGGGCCGTCGGACCGCGCAGGCGGAGGTGGGGCTGCCGCTCCTCGTCGCGCGGGTGCCGACCTCGAAGGAGGTCGTCTTTCTCGCGTTCGACGGCGGCTGGAACCACGATCCGGCGGCGGCCCGGATCCTGCTGGACCGGCGGGTACCCGTCTCGCTGTTCTCGCTGCCGGGTGCAGCCTCTTACGACGCCGGGTACTTCACCGGGCTCACGCAGGAGGGACGGGCGGGCGTGGAGAACGACACCGTCACCCATCCGGACCTCACGACGCTCGACGCTGCCGGCAGGGTTGCCGATGCGGGGCGGGGGAGCAGCTCCGGGTTGTCTTCGGGCGGGTGCCGAAGCCTCTGTGGCCGCCGTACGGGCGGTGAACTACGAGGTGCGGCTCGCGGCCAAGGCGTGCGGGGTGAAGGCGCTGGTCACCTGGACACACGACTTGACCACCTGGGGTGATGTGCCGCCGCCCACGCCGCGGCCGGAGTCGGGCGACATCGTGCTGCTGCACTTCTGCGGCGGGCCTGGAGGCGGCGAGGGCCGTCGGCCTGAGGGCCGGCGGTCATGATGCCGCAGCTGAGAGGTGTCGGGGGCGGCCTACAGCTCGCGGTGGACCTTCGTGTTCGAGGCCTGGGCGCGGGGGCGGACCACCAGGAGGTCGATGTTGACGTGGCTGGGGCGGGTGACGGCCCAGGTGATGGTGTCGGCCACGTCGTCGGCGGTCAGGGGCTCGGCGACGCCCGCGTAGACCTTCTCGGCCTTCTCCGCGTCGCCGCGGAAGCGGGTCTTCGCGAACTCCTCCGTCCGGACCATGCCGGGGGCGATCTCGATGACGCGCACCGGCTGGCCGACGATCTCCAGGCGGAGGGTCTCGGCGAGGACGCGGGCGCCGTTCTTGGCGGCGACGTAGCCGGCGCCGCCCTCGTACGTGGCGTGGCCGGCGGTGGAGGAGAGGACCACGACCGTGCCGTCGCCGGAGGCGGTGAGGGCGGGGAGGAGGGCCTGGGTGACGTTGAGCGTGCCGATGACGTTGACCTCGTACATGGTGCGCCAGTCGGCGGGGTCGCCGGTGGCGACGGGCTCGGCGCCGATGGCGCCGCCCGCGTTGTTGACGAGTACGTCGACGGAGGGGTAGCGGTCGAGTGAGGCGGCGAGGGCGTCGACGGCGGCGCGGTCGGTGACGTCGAGGGCGTGCGCGGTCGCGGAGTGGCCGGCCCCGGTGAGCTCGGCGGCGAGGGCCTCGATGCGGTCCTTGCGGCGGGCCGTGAGGACGACGTGGTAGCCGGCCGCGGCGAGCTGCCGGGCGGTGGCCGCGCCGATGCCGCTGCTCGCGCCGGTGACTACGGCGGTTCGGGTGGCGGCCGTGCTCATGTGCGGGCTCCTCGGTCGTTCGTACGGGCGATCACCCGCCAGCATAGGCGCGGCGGGGCGGCTCAGCGGCCGCGCGGGGCGTACATGATCACGGCCATGCCGGCGAGGCAGACGAGGGCGCCGACGACGTCCCAGCGGTCGGGGCGGTAGCCGTCGGCGAGGGCCCCCCAGGCGAGGGAGCCGGCGACGAAGACGCCGCCGTAGGCGGCGAGGACCCGGGCGAAGTCGCCCTGGGGCTGGAGGGTGGCGACGAAGCCGTAGAGGCCGAGGGCGATCACGCCGGCGCCGATCCAGGCCCATCCCCTGTGCTCGCGCACGCCCTGCCAGACGAGCCAGGCGCCGCCGATCTCCAGGAGGGCGGCGAGGGAGAAGAGGGCGGCGGAGCGGGCGATCAGCATGGCTCAAAGGTACGCAGGGCAGATGGGGGAGGGCGCGCCCTCGTTCGTGTGATGGTCCGACTTTTCGGGCTCGTTGGGGTCTAGCCTCCGCGCGAGAACGCGAGACGCGAGACCGAGACACGAGGAGGAGGTGGTGGCGGTGCGCCGTGTCGCCGTACGGAGTGTGGTGGTGGCGGGGTTGCTGGCGCTCGGGGCGGGTGTGCCCGGGCCGTCGCAGGCGTGGGGTTCGGGGTGGGCCGGGCCGGAGGCCGACGTGTCGTACCACGGCCGGGTGGCCCTGGCCGGGTCGCAGCTGCGGGTCCTGCTGGTTCCGGAGAACGACGGGCCGGCCGCGCTGGCGAACGCGACGCTGCGGGTGCGGTTGTCGGCGGACCTTGCGGACCGGCAGCAGCTGCCGCAGGGATGCGCGCAAGCCGGGCTGCGGGAGGTGGTGTGCGAGACGGGGCCGTTGCCGCTGCAGGGGCGGGGCCGGCACGTGGGGCTGGCACTGGAGCTGCGGGAGCGGGTGCCCGAGGTGGTGGTGCGGGTGGACACGTGGTGGAACGGTGGTGCGACGGACCGGAACCGCGCGAACAACGAGCACGTGGTGCTGGCCCTGGACACGGGTGACACCTACGCCTTCTGAGGGCGGGCCGGGCGCGCCGGGCGGGCCCGGCGGTCGCGGTCGTCAGGCGGTGCCGAATTCGACCAGTGCCTCGTCGACGATCCGCTCCAGCCGGGCGTGGTGGGCGCCGCGCCAGTAGACGCGCTCGCATGCGGCGCACTGCGCGAAGACGTCGTAGGAACGGTGCGTGCCGTGTTCCAGGCGGTCGCCGACGCTCTCCTTGTCGGCTTCGTGGAGCGGGCCGTTGCAGGCGGTGCAGCGGGTCCACGGGGCCAGGGCGGGCGCGAAGCGGCCCAGGACGTCGCGCAGTTGCTCGTCGGGGTTGTCGCTGTAGATGTACGCGCCGGCGAAGATCTCACGGCGGCGGAGCAGGCCGCGGTCGCGCGAGAGCAGGACGCGCCGTTCGGCGGCGGACCGGGTGGCGAGGGCGGGGTCGCCGATGTCCTCGTTCTCGTAGGCGGCGTCGACGCCGAGCAGGCGCAGGCGGCGGGCGAGCGTGCCGAGGTGGACGTCGAGGAGGAAGCGGAGGGGGGCGCCGGGGACCTGCTGGGGGCGCTCCACGCCGAACACCTCGACGCTCTGGCCGTCTTGGGGCACGTAGGAGACGGGGACCTCGTGGCCGTCGACGAGGAGGCGGCCGACCTCGGTGAGCGGGACCCCCGCGGATTCGACGACGTGGCCGAGGCTGGAGGCGCCGTCGGTGGCCGTCGGGACGCGGTCCGCGCGCCGGCTGGGCGGGGCGAAGAGGCGCAGTTCGGGGGCGAGGGTGAGCTGAATGCCGGGTCCGTTCACCCTGTCAGCATGCCATTGCGGGGCGGCTGGTCGAGCCTGATTTCAGGAGGCCGCGGCGGCCCGGTCGTAGGTGTCGCGGTGGGCGCTGACCTCGTCGAAGTGGTTCTCGGCCCAGACCTTCACCGAGGAGAGCAGGTTGCCGAGGCTGCTGCCGAGGTCCGTGAGCCGGTAGTCGACGCGGACGGGGACGGTGGGGGTGACGTGGCGGGTGACGAGGCCGTCGCGTTCGAGGGAGCGCAGGGTCTGGGTGAGCATCTTCTGGCTGACGCCGGGGATCTTGCGGCCGAGGTCGCTGTAGCGCATGGAGCGGTCGTCGGCCTCGCCGAGGGCGCTGACGACGAGGCCGACCCACTTGTCGCTGATCCGGGCCAGGAGCTGGCCGGTGGGGCACTCCTTGAGGAAGGCGTCGTAGGCGGAACGGGCTTCTTCGCGGCGGGCCGCGGCGGTGCTGGTGGCCATGGGCACCCACTTCCAGGTCCGGTACGCACCTTCGAGTGCGTACTTACGAAAGGAGAGTACCTCTCCCTAGGTTAGTGGTCATCGGAACGAGCGAAGACGACGGAACGGGGAGAACGATGAGTGAGCGGACGATGCTGGCGGCTGTGGTGACCGGGTTCGGCGGCCCGGAGCGGGTCGAACTGGCCGAGGTGCCGGTGCCCCGTCCGGAGGCCGGCCAGGTCAGGATCCGGGTCGCGGCCGCCGGCCTCAACCCGGTGGACGCAGGGGTCCGCGCCGGGATCTTCGGCGGCGCCGGTCAGCGGCTCGGCCTCGGCTGGGACGTCGCCGGCGAGATCGACGAGACCGGCCCGGAGGTGACCGGCTGGAGCCGCGGCGACCGGGTGGTGGGCCTGCACTACGGCCCGGTGAAGCCGCTGGGCACGCACGCCGAGTACGCGGTGCTCGACGCCGCCGCGGTGGCCGCCGCGCCGGCCGCGGTGGACGACCTGGCCGCTGCGGCGCTGCCGCTGGCCGGCCTGACCGCCGCCCGCGCCGTGGAGCAGCTGGGGCTCGCCCCCGGCTCCTCGGTGCTGGTCACCGGCGCCGCGGGTGTGGTCGGCGGCCTGGCGGTGCAGCTCGCCGCGCGGGCCGGCCTGGTGGTGACCGCCCTGGCGGGGCCGGGGGACGAGGAGCTCGTACGGTCGCTGGGCGCGGCCGCCTTCGTCCCGCGCGGCGGGGCTCCGGCCGGGCCGGTGGACGGGGTCCTGGACGCGGCGGTCCTGGGCGGGGCCGCGCTGGCCCGGGTCCGCGACGGCGGGGTCTACGTGGGCCTGATCCCGAACCACGCCCCGGCGGCGGAGCGCGGCATCCGGGTGGAGGAGCAGGAGGTCGCCGCGGACGGGGAACTGCTGGCCCGCCTGGTGTCCCTCGTCGACGAGGGCGCGCTCACGCTCCGGGTCGGGGACGTCTTCCCGCTCGCGGAGGCGGCGAAGGCGCACGAGCGGCTCGCGGCGCCGGGGGTGCGCGGGCGGATCATATTGACGGCGTGACCGTGACCGATGCCGGGGCCTTGGCCCCTTCTCCCTCATGGAGCAACCCTGTGAACGGCAGCGGTTCATGACTGCATGTCAAGGGGCGCCTCCACGGTGTGACGAAGGGGCGTCGGGGTGCGGCCGGGGGCGGCGGACGCCGAGATTTTCTTACGCGTGTTCGTGGCTCGTCCGGGTGGCGCACATCCGGACAGTGCCCGCCTGTGCCGCCCCGCCGCGCCCCGGGCGTGGCTGACCTGCGCCGGGTCCCTGGCCGAAGCGCGGGCGGCGCACCGAAATGGAGGGCGGCCGAGGCGGATATCGAACACTGAATGATCAATTCCAAACGCCAACGGTCCCTGTTGCAAAGGGAATTGACCTTTGACTTCCGATCGGCGTGGCCTAGCCTGGCTATCAGCCGACCGGGGGGAAGGGCTTCGGCTGCCCTGCCCTCTCACTGCATCAGTCACCACCCGACGAGGGGGAGTAACGAGTGCTCAGTAAGAGGATTTCGGCCGGATTCATCGCGATGGCGGCCGTCGCCGGCGTCGTCGCCGCGGCACCGTCCGCATCGGCCGTGGACCGTACCTGCTACGACGGCAATTTCTGCATCTACAAGGACCGGGACTTCTCCAAGAACAACTCGATGTACCGGACGAAGTACGAGTCCGCGCGCTGGGACATCGACATGCCGGCCGTCTACGAGGCCGACAGCTCCTGGTGGAACCGGCGCGGCCAGTCCTCCAAGACCTACGGCGGTCGCTGGATGTCTCTGGGCGTCGAAATCTGTCTCATTCCCGGTGGTTCCGTGAACTACTACTGGGACGCCAACGACGATGGTGCGAGCAACACGCTGAACGACGGCTCGCGCTGCTGACCATCGCTCGAAGGCCGGGCCGCCCCCGCAGCCGCGGGGGCGGCCCGGCCGCACCCTCCGGAGGACACGGACATTGAACAAGCGCACCCGGGTTGTGACGGCGATCGCGGTGGTGGCGGTGTTGACAGGCTCCGCCTCCGCCTGCTCGGAGGAGTCCCCCAAGGACATGGAGACGGCCCGCCGGGCCCAGGCCGCGCTCGACAGTGCCAACGAGGCGCTGGATCAGGAGCGTGAGGCCGAGACCAAGCTGATCCGCAAGTGCATGAACGACCAGGGCTTCAAGGTCTTCCCGTCCGACGGCGCCAACAGCAACAAGGGCGGGAAACGCAGCGAGGACCTCACCCCGACGTCCGAGGCCGCGCGCACCGTGGGCTACGGCGCGGACCCGCGCCGGTCGGAGAACCAGAAGACCCAGGAGGCCGGCGACGACTTCGACGCGCTGCCCGAGGACGTCAAGCGGGCCCACAGCATGGCCATGGACGGCTACGTCGACAAGCCCGAGGGCGGGGTCGAGTTCGACTTCGGCGGCGGCAAGGTCATGGTGCCGTCGAAGGGCTGCCGCGGCGAGACCCTCAAGGCCGTGTACGGGGACGTGAAGGAATACCTGCGGCTCAACTGGACGGTGTACAACACCGTGAAACAGGACAGCGCGCGCATTCTCGGCGACGACGACGCATATCAGAAGGCGTTGTCGGAATGGGCCTCCTGCATGAAGGCCGGCGGCTATCCGGAGATTCCGACTCCCGAGAAGGCCAGGGAGGCGGCGCTTTCGCATTATGCGAACGTCCCGGACGGTGATACCGCGGCGCTCGACAATGCGCAGCGCGCCGAGATCAAGCAGGCCACCACCGATGCCGATTGCGGTACGAAGGTCGGGCTCAACACGAAGGCGCGGGAGGCGAAGAGCAAGGCGTCCGCCGATTCGCTGGTGAAGCACGAAGCGGAGATCACCGCCTGGCTGGAACTCATCACGAAAGCCAAGGCCAAGGCACAGGAACTACTGCGAGAGACGTCGTAATACCGTGATGAGCCTCGAACACCCCGAGGGGCCCCAGGCGGCCGAGCCGTCCGGCGGGCGGGCCCGGCACCGGTCCAGGAGGGCCCTCGTCATCGCCGCCGCCGTCGTCGTGCTGTTCGGAAGTTCCGGATCGGTCTGGTGGATCGCGTCCCAGGCCAGAACACCCGAGCAGCGTGCCTCGAACGCGGCGGCGCCGCCGCCCTCCCGGATCACGGGGAAGGTCTCAGACCAGCAGCTCGTCGAGAAGATGGAACTGACCGGGAAGGTCGAGACGGCCTCACGGACCACCATCGCCGGCGTCCAGCCGCAGGGCACCAGCCGCGCGGTCGTGACGGGCCTGCCCGCGGCCATGGGCAAGACCCTCAAGGCCGGCGCGGTCGTCGCCGAGGTGTCCGGCCGGCCGGTCCTGCTGCTCCCGGGGCGCTTCCCCGCGTACCGGGACCTGAAGGCGGGTGACAAGGGCCCGGACGTCCAGCAACTGCAGCGCGCGCTGCAGCCGTTGTACGGGACCGCCGTGAACGGCACGTACGGACCGGCCACCGTCGAGGCGGTACGCAAGCTGTACGCGGCGGCCGGGTACGAGGCGCCCTCCGGGCAGGGCCAGAGCCAGGGTGGCGGCGGTGCCGGCGGGGGCGGTACGGGCGGGGGCGGTGCCCCGTCCGGCGCGTCCGGCGGCGGCAGCGCGCCCCGCGGCGGCGCGGAGACCGACGGCGGCACAGGCGCGGCCCCGCGCACCAAGGCAGGCGCGAGCGCGCCGCCCGCCCGCGGCTCCGACGCGCCGCCGGGCTCCGGACCCGCCAAGGCCGGGGAACTGCTGCCGGCCGCGGAGGTCGCGTACGTCAGCACCCTGCCCGCCACGGTGGTGCAGGTCACCGCGGCGGTCGGGGACGCGGCCGACAAGCCGCTCGTCGTCCTCGGCAGCGGCGGCCGCCAGGTGCGGGCGACCCTCACCGCGGACCAGCGCACCCGGCTGCGCGATCTGCCGGACGACGCGGTGATCCGCTTCGGCACCGGCCCCTACGAGGGCCGGGAAGGCAGCCTGGGCTCCCTCGCCGGCCCCGCCGACGCCAAGAGCGGCGAGCAGCAGGGGAACGCGAAGACCGGCGGACAGGAGGGCGCAGGCACGTCCGGCGCCGCGGGTACGGCGGGTACGGCGGGCGGGGGAGGCGGCAACGGCGCGAGTGGCGGTGGGGGTGGTGGCGGTGGCGCAGGCCAGCACGAGGCGCTGTTCGTCCCCAGCGGGGCCGAGGCCAAGGAGGGCGCGGTCCAGCAGATCAGCGTGGAGCTGCGGCGCAGCCCCAAGGGCGCGCTGACCGTTCCGGTGTCGGCCGTGTGGACCGACCTCGGCGGCGGGTCCACGGTCACCGTCAGCGACGGCGGCAAGGAGCGCGACGTCCCTGTCGAGGTGCTGTTCACCCATGAGGGGCTCACCGCGGTCACCGCGCTCGACGCGAACCTCGGCGCCGGCGAGACGGTCGTCCTCGTACGCCGCGGAAAGACGGCGGACGGCGCCGAAGGGGGCACCGATGACTGACCCGGCCGGCAGCCCGGCGGCCGGCCGGGCTGTCGACCCGGCGGCCGGTCCGGCCGGCGGCCCGGCTCTCGACCCGGCCCCCGTCATCGAGATGGCCGGCATCGCCAAGACGTACCCGGGGCCGCCGCCCGTGCACGCGCTCACCGACGTCACGCTCGACATCCGGCCCGGCCGGCTCGCCGCGATCGTCGGCCCCTCCGGCTCGGGGAAGTCCACGCTGCTGAGCGTGCTCGGACTGCTCGACGTCCCCACCCGCGGCCGCTACCTGCTGCAGGGCAGGGACACCACCGCCCTGTCCGAACGGGCCCGCACCGCGCTGCGCGCCTCGACGCTCGGCTTCGTCTTCCAGGCCTTCCACCTGGTCCCGCACCTCACCTGCGTACAGAACGTGGCCCTGCCGCTCGTGCACCTCGGCGTGCCCCGCGCCCTGCGGCGGCCCCAGGCCGTGGCCGCCCTGGAATCCGTGGGCCTCGGACACCGCCTCGACGTCCGGCCCACCACCCTGTCCGGCGGGGAGCGGCAGCGGGTCGCGGTCGCGCGGGCGATCGTCCACCGGCCCGCCGTGGTGCTCTGCGACGAGCCGACCGGCAACCTGGACACCGCCAACTCCGCCCGCGTCATGGACCTGCTGACCGGACTGGTGGCGCAGGACCGGGCCGTCGTCGTCGTCACGCACGAACCCGAGGTCGCCGCCCGCGCCGACCGCGTCTTCAAGGTGGTGGACGGCCGTGTTTCGTAGCCGCAGGACGCGTGAGCGGTCCGCGGACGTGGAAGCCGGATCGGACGCGGAGGGGACGGCGCCCGCGGCCCCCCGGACGTCCGCCGCGGACCTGCTCGTCCAGGCGTTCCTCGCGCTGTTCGGCCGCAGGTTCCGCACCCTGCTGACGATGGTGGGCATCTCTGTGGGGCTGGCCGCGGCACTCGCCACGCTGGGCATCACCGCCAGTGCGGCCGGCGCCGTCTCCGACCAGTTCGACGCCCTCAAGGCGACCCGGGTGACGGTCAAGTACCCGTCGGAACCGGTCGCCGGGGTCCGGCCGCGGCCCGACGGCGGTGACACCCAGCGGGTACGCGGCCTCAACGGCGTCCGCACCGCGGGTCTCGTCAGCAAGGCCGGTGAGCAGCCGGTGGTCTCCCGGCTGGCGTCGGGCGGGTCGAACGACCTGCCCGAGGGGACGGTCCTGGCCGCCCAGCCCGACGCCCTGCCGGCCATGTCGGCCGAACTCACCCAGGGCCGGTGGTTCGACACCGGGCACGACGCGCGGCGGGAGCGGGTGGCGCTGATCGACACGGCCGCCGCGTCCCGGCTGACCGTCGACGGCGGGGCCGGCAACTCCGTGATCCACGTCAACGGTGTCGCGTTCAGCGTGCTCGGCGTCTTCCGCGCCCCCACCGGCGACACCGACCTCACCGGCTCCGTCGTCGTCCCCTACTGGGCGGCCCTCCAGGACCCGGCCGGTCTGGGCTTCGCCCCCGCCGAAATGATCATCCGTACGGATCTGGGTGCCGCCGACCAGATCGGCGCCGAGGCCCCCTTCGCCCTGGCCCCGGGCGCACCGGACAAGCTGGTCGCGCTGGTGCCGCCGGACCCCCGGTCGCTGCGCCAGGGCGTCGAGTCGCAGACCCGGGCCCTGTTCCTGGGCCTGGCCGCCGTCTCCCTGGGCGTGGGCGCGCTGGGTGTCAGCAACACCGCCTACGTGTCCGTCCTGGAGCGGCGCTCGGAGATCGGCCTGCGCCGTGCCCTGGGTGCCTCCCGGCGGGCGGTCGCCGGGCAGTTCTGCATCGAGAGCGGTCTGGTCGGGCTCGCCGGCGGTGTCGTCGGCACGGTCCTGGGCATCCAGATCACGGCCGTGACCTGCCTGGCCAAGAACTGGCTGGTGGTCCTCGACCCCGTCCTGACGACGGCGGGGCCGCTGGTGGGCCTCGTGGTGGGGCTGGCCGCCGGGCTGTACCCGGCCCTGGCGGCCGCCCGTATCCTGCCCGCCGAGACGCTCCGCGCGGGCGTGTAGGCGGGGCGGTGTCGCGTCGGCGGTGTTTCAGCTGCCTCAGCCGCGCTGGAAGAACTCCACCTCCGCCAGGGCGAGAGGGCGCTCCGGGGCCGAACCGGCGGGCTCCTGGAGGGTCAGCCGGACCGTCGCGACATCGCTGATGCCGGTGGGGAACGTCTGCGGGCCCGGCTTGTCGCTGAGGACGAGCTGCTTGTGGACCGTGGCGCCGTCCCGGTCGGTGACCTCCATGTCGATCCGCAGTGCCCGGCCCTGCTTCGCGTACTCCTCGGGGGCGGGCGAGGCGCCGTTGGTGATGATCACGGCGACCAGGCGGAACGGCTTGCCGAAGGTGTACGTCGCCGAGGTGCCGGGGCCGGGCGCGGCCCAGTAGCGGTTGCTGAGGCCGTCCGTGCTCAGGCCCACGGGGTGCCCGGGGAGTTCGGCGCTCGCCTGGGCGCGGGTCGGGGTGACGGCCTTGGCCTTGCCGAGCTTGTCCAGGGTGTCCTGCACGAGGTGCTGTCCGGCGGGCAGCAGCAGGAACCCGGCCGCGCACAGGGCCAGTACGACGGTCAGGACCACCAGGAAGCGGACCAGGCGGCCGGAGCCGGCCCGGGTCCGGCGGCGCAGCGGCCAGACCGTGCGCCACCAGGGCAGCGGGGCCGCGATGGTGGAGGGCGTCAGCGGAGCCGCGCAGCGGCGGCAGAAACGGCGGTCCGGCGGGTTGGGCGTGCCGCAGGCCGGGCACGGCACCCCGGCGACGTCGTCGCTCACGGCGAGGGGACGTACGACGGGCCGCGGCGCGACGGGCATGGCCGGCAGGACAGGGGCCGGGGACGCCGGCGCCGGGTGTGCCGGGGCGCGCGGCGCGGGCTGGGCCGGGCGCGCCGGAGCCACCGGCGCGGGCCCGGGCCCGGCGGATGGCGCCGCCGCTCCCGCGGGCGCGACCGAACCGGACTCCGCCCCGGCGGGCTGTGTGGGCGCGACCTGGCCGGGCCGCCTGCGCAGCCAGGACAACCACCGATCCGCGACGCCGGACTCGGGTGCGGCCGACTCCGCCCCGGGCGTGTCCCCGCGGCCTCTGCCGCCCGGCGGGGTGCCCTGCCCGGGCGCGCCGCCCTCCGGGGGCGTGCCCCGCCGGGAGGCGGCCCCTCGCGCGGTGCCCGCGCCACCTCTTCCGTCCGGGGGCGTGCCCTCCTGCGGCGCGCCGCCGTCGGAGGCTGCCTCCCGCGCCGCACCCCCTCCGGCGGTTCCGCCCCGGGGTGCGCCGGTGGGTGCCGTTCGGGCTGTGTCCCGCTGGGGGGTTCCGCCCGGCGGGGTGGTTGCGTGCGAGGGGGTCGGCTGCTGGGTGGTGGCCGCGCCGGGTATGCCGCCTTGCGGGGTGGCCTCGTGGGCGGTTCCGTCCCGGGGTGCGCGGGTGGGTGCCGTTCGGGCTGTGTCCTGGTGGGGGGTTCCGCCCGGCGGGGTGGGCTCTTGGGGCGTGGCGGAGCCGGGCGTGGGGCGGTCCTGGGCCGTGCTCCGCCGAGGCACGTCGGGGTGGGGTGCGCCGCCCCGGGGGGTGCCTTCCGCGGTCGTGCCCTGCTGGGGCGCGCCGCCTGGCGGGGTGCTCTCGTGGGGCGTTGCGTCTTCGGCCGTCTCCTGCCGGGATGTGCCGCCTCGGGCCGGCGCCGCCCCCTGGACCGTGCCCTGCCCGGCCGTGTCCCGCCGGGTGGCCGTCTCCTGCGCGGTGGCCGGCGGGGACGTCGCGGGCCCGGACGTCGCGTTACCGGGGGTGCTCCCCTGGGGCAGGCCTTCCCGGGGTGGGGCGGTCTCCTCGGCCGCGCTGTCCCCGGGTGTGCCGGCCCGGTCGGTGGCTCCCCCGGTGGCCCCTTGGGGCGCGGCTTCACCGGGTGTGCCGGCCGGGCCGGTCCCGGGCGGGGTCCGGCCGGGGGCGTGCCCGGGCGGCCTCCCCGGCCGGGGCGGCGGCCGAGGGGGAGGGGGTGGAGGAGGACCAGTTGAGGTAGGCGCCGCAGTTGGCGCAGAAGTCGTCCGTCGGGGCGTTGGAGGCCCCGCACGCGGGACAGGCGCGCATGGCCGTCAGCTCCCTTCGGGCGCGGGCGGGCCGGGCAGGATCTCCACCCGGCAGACCGTGTGCACGGGGCACAGGGCGCGGACGAGGGCGTGGACCCGCTCGGCGTCCACCCCGTGCGCGGGGTTCGTGCCGCGCGGCCACACCCGTACGAGGACTTCGCCGGCCGCCACGGGGGTCGGCTCGGTACCGGCCGTGCGGGACCAGACGGCCCCGCCGTCGCCGCTGACGTCGGCGGACACGCCGAGGACCAGGCGCAGGGCCTCGACCAGGCCGCGCCGGGTGCCGCGCCACCGGTGCAGTTCCACCGCGCGGGCCACCGCCTCGCGCCGCAGGGCGGCCGGCCAGTCGGGGTCGTCCGCGCCGCCGACCCAGGAGGCCAGCCAGGACAGGAAGTCGGCCGGTGCCAGCCGGGGGTCGAAGTACGCGGGCAGGTTGTCGAGGGTCGTGAACACCGGGGCCAGGACGGTGTCCAGGCCGGCCGTGAACCGCTGGGCGAAGTCGTCGTCGGCGTACAGCGCGGGCAGTTGCCCGCCGATCGGGTGCCGGCTGGGCAGGCCGGGTACGGCGGCGCGGCTCATCCGTGCACCTCCGGCTCCGCCACGACGACCTGGTGCTGGTAGGAGAAGACGAGCGTGCCCGCGCCGATGTCGATGCGGTCGACCGGGGCACCGCGCCGCCCCGTGATCGGGTCGGCGGCGAACAGCCGGATCTCCTCCACCAGGACGTCCCCGACGGCGCGTTGCAGCACGCCGAACACCTCGCCGTACTGCACGGGCCGGCCGAACGGCCAGCCGGTGCCGTCGGGTCCGCCGTGCAGCGGGTTGAGGTGCCGAAACAGTGCGGCGAGCGCCGCGTCGCGTATCCGGTCGGCGTCGGCGGCGGGCGCCGACAGCCGGGCGACGACCGTGACGCCCTGGTAGGCGGGGGGTTCCACCACGAGGCCGGTGCCGATCAGGCGCCGCTCGTCGAGGGCCGTGGTGATCGCGGCGAGGACCTGGTCGGAGGGGATCAGCTGCTCGAAGCGGAGCCGGTCGCCCTCGTCGGCGACCGCGTCGGGCACCACCAGGACGCGTGCGGAGCCCGCGCCGCGCCCGCCGTCCGTGGCGGGCAGGCAGCGCACCCGGCGCACCGAGGGCGCCGCCCGGCGGGCGATGATCTCGTAGTCCTCGGCGGTGACCGCGCGTTCCTGCATGCGCAGCGCCTCCGGGGCGCGCAGTTTGGCGTTGTCGACGGTCTCGCCGGCGACGCCGCCGCGGGCCGCCTCCCGGTTGGCGACCCGGGCTATGTAGGGGACGGAGCTGCGCAGTACGGAGATCGCGCCGCGTGAGACGTTGCCCGCCGGGCCGCCGCCCGTGCGGTAGCGGGCCACGCGGATCCGGGAGCCCTTGGGCGGTACGGCGCCGCAGGCGCGCAGGCTGCCGTCGGCCTCGCGCAGCACCGGCGGGAAGGAGAACTCGCCGGTGGTGGCGTCCACGCGGACGTGCCGGTCGTCGGGCCCGGAGCGGCCGAAGTGTTCGACGACGTCCCAGCGCTGCCAGCCCTCGGGGGAGGACACCTCCACCACCGGGGGTTCCCCGTCGAGGAGGACGGGCGGGCGGCCGAGGCGGAAGCTCTGCCCGGCCACGCCCTCCGACGCGCCGAGCGGTACGTCGCTCACGCGTTCGGCGTGTTCCACGGTCATGGTGCCGCCGACGGTGAAGACGGCGGCCTCGCGCACGGTGGGGGACTCGGAGTAGAAGGGCTGGCCCGGTTCGGGTTCGGTGACCCGGCAGCGCAGCCAGCCCGCGCGGGTCCCGCTGATCACCGACGCGGTGTGCCCGGCCGGGACGTAGACGATGATCTCGCCGGGCCGGTTGAGGCCGCCGGTGCTGTCGGAGTCGGTGGCGCAGCGCTGCCAGCGGCCGCCGTCCCAGGCCTCCCACACCAGCGGGGGCTGGCGCGGGTCGACGCCGACGCCTTCGACGCGGCTGTCGAGGCGCACCGCGACGATGCAGCGGGGGACCGCGGTGGGCAGGCCGAAGAGCACGGCGTCGCCGGGTTCGGGTGTCGCCTGGAAGCACGGTATGCCGCGGCCCTCGGCGAGTGCGCCCGTGCGGTCGGCGGGCTCGCCCGTGCGGGGCGCGGTGACCAGTTTCGTCAGCTCGCTGGGCAGGATCCGCAGGTCGCCGGTGGTGGCGAAGACCACGGCCTCCTCGCTGTCGCCGGCCGAGGTGGTCACCTCGGTGGTCACCTCGGTGCCCGCGGGCAGGGTGACGGTGTCGGGCTGGGGGGCGGACAGCCAGAAGTCGACGTCGGCGGAGGCGGCCGAGGGCGGGTACAGCTGGATGCCCAGCAGGTCGAGGAAGGCCAGGTAGTTCTTCTCGGGGACCCGGTTGAGCCGGTACAGCAGCTGGTCCACGAGGTAGGCGAACGTCTCGATGAGGGTGACGCCCGGGTCGGAGACGTTGTGGTCGGTCCACTCCGGGGCGCGCTGCTGCACGTACCGCTTCGCCTCGTCGACGAGCTGCTGGAACCGTCGGTCGTCCAGGTTGGGGGAGGGCAGGGCCATCAGTCCGCGACCATTTCCTCGGCCCCCTCCTCGGAGGGGATCGTGTAGAAGGGGAAGACCAGGTTGCGCCGGTCGTTGGTGGTGCGCACCGTGTAGTGCACATCGATGTAGAGGGTGCCCGCCTCGACGGAGTCGAAGGCGACGACGACGTCGTCGACGGTGATGCGGGGCTCCCAGCGTTCCAGGGCCTCGCGGACCTGCTGGGCGACGCGTCCGGCGGTGTCGCCGTCGCCGGGGGCGAAGACGTACTCGTGGATGCCGCAGCCGAATTCGGGCCGCATGGGCCGTTCGCCGGGCGCGGTGCCCAGGACGAGGCGGATGGCCTCCTCCAGCTCGCGTTCGCGGTCGACCATGGCGATCCCGCCGGTGGGGCCGACCCGCAGGGGGAACGCCCAGCCGCGTCCGATGAACCGTTCGCTCATCACACGCCTCCGATCAGGACGTCGAGGGCGCCGGTGAGGACCATCGCGCCGCAGGCCGTCTGGTCGCGGGCCCGGGCGGCGGGCAGCCCGCCGATGAGGACGGTGCCCGAGGCGAGGGCGGCCGGGTTCGGGACGATCACATTGGCCGGTCCGAGGGCGGCGTGCGGCGGGACCACGCAGACGTGCAGGCTGCCCACGACGGCGGCGGGCCGGCCGCCGATCAGCACCGTGGCCACCTGCGCGGCGGCGCCGGGCGGTGGCGTGGCGAGCCGGCCACCGTGGTTGGTGGGGTCGCCGGTACGGGCTGCGGCTGGCATCGGGGCTCCTCGGGGGCGGCGGTGGCGGCGTAGGGGGGGCGGGGGCTGGGGCGGGCGTCAGTTGATGCGGATGAGGCGGGCCTTGAGGACGGCGAGCAGGCCGCCGTTGACCGTGACGTCCGAGGTTCCGGAGACCTTCACCGACCGGCCGCCGATGCTGACGCCGGCGGTGCCGTCGATGTCCACCTGGCGGCCGGACACCTTCACGGTGCCCTGCCGGGCGTCGAGGGTGATGCCCTTGCCGTCCATGAGGACGGACGTCAGCGGGCGGCCCCGGCCCGCGTACACGGTGAGTTCGATCCGGTCCCGGCGGTCGTCCATGCGTACTTCGAGCCGCTCGTCCCCGGTGACCAGCCGCAGCCCGGAGGGGCCCGGCGCCGCCGCGTCCAGCAGTTCCACGCGGTGGCCCGAACGCGACACGATCGAGCGGCGGTTGACCTTGCCGCTGGTCCTGTCGATCAGCGGCACGTCGTGCGGTGAGGGCTGGTCGACGCCGTTGTAGAGGCCGCCGATGACGTACGGGCTGTCGAGCAGGCCCTGCTCGAAGCCGACGAGCACCTCGTCGTTGACCTCGGGGCTGACCACGCCGCCGCCCCCCTTGCCGCCCCACTGGACGGTGCGGACCCAGTCGGTGGTGTACGTGTCGTCCAGCCACGGGAACTTCAGTCGGACCGCGCCGCGCTGGGAGCCGTTCGGCTCGCGCACGTCCGTGACCACGCCGATCGCCAGACCGGGGATGCGCGGCCCGCGCCCCGGCGCGTTGGCGCCGGTCACCAGGCCGGTCAGGGAGCGGTCGGGGCTGGCGCTGACCCACACGGTCGTGCGGAAGCCGCCGTGCGGCTCCAGGACGTGCTGGACGGCCGTGGCCGTGTACCGGCCGGAGAACGCCGGCCCGACGTTGCCGAGCGCCACGGGTTTGCCGGCCCGCAGCAGCGGGTTGCCCTCGGCCACCGCCTCCAGTTCGCCGAAGCCGGAGCTGATCTGCGCCGCCGTCGCCTTCGCGACCGCGGTCGTCTCGGCCTGTGTGCGGTAGGGGGTGTCGGTGACGGACACCGACGCCGCCCCGAAGCGGGCGGCGGTCTGCGGGCCGAGGCCCGGCACCACCGTGTCGCTGACGACGGACGGCTGCTCGGCGACGAGCGGCCGCTTCGTGGTGACGTCCCAGCCGCGGACCTGCACCTTCGAGGCGCCGTCGGCGGCCGACAGGGCGGCCCGCAGGGCGAGGAGGTTGCGCCCGTACTCCAGGACCATCGGGTCACGCACCGCCGACGTCGACGGGGCGGGCGCCCCGGACGCCTTCACGGGCCGGGTGAACTGCAGCAGGCCCTTGTCGTCGACGCGTACCTGTGCGCCGCTCTCCCCGGCGAGGAACTGCAGGAAGTCCCAGTCGGAGACGTTCGCCTGGGACAGCTGCTTGTACGTGACCGGCGCGGCCTCCACCTTCCCGACGGCAAGGCCCGCTCCGGCGGCCACCTTGCGGACGATGGCGGCGGCCGTCATGTTCCGGTACGCGACGACCTTGCGGCCGCGCTGGAGGCGGTGCGCCTTGGAGTAGGCGCGTACGACGGTGAACGAGCCGGTGCGGTCCCGGTCGATCTCCAGGGCCGTGACCTCGCCGTTGAACAGCCGTTCCCGGGCCTGCCCCTTCACGGTCGCCACCGACACCCGCAGCGGGGTGCCGATGGTGATGCCGGTGGCGCGCAGGAACTCGTGGTCGGGGTCGCGGTAGGTGAGCACCGCGGTGTCGGGCAGGCCCACGTTCTCGTCGACGACGCAGGAGACCAGCTGCGCCGCCCAGATCTGCGGCAGTTCGCCGGGGGCCTCCACGATGGGGTCGGCCGCGAACGACCGGCCTCCGGGCTCGGATCCGCTCACCGCTGTTCCTCCTCGCCGTGCTGGTCACGCGTGCCCGGCACCACGATCTCGGTGCCGGGGACGAGCGCCATCGGGTCGTCGATGCCGTTGGCCTCCGCGATGACCCGCCAGGCCGTCGCGTCGCCGTATTCGCGCCAGGCCAGCATGGCCAGGCTGTCGCCCGCGACCACGGTGTGCGTGCTGCGGGCGGTGCGGGAGCCGGAGGTCGGGTTCTGGCCGGGCGGGTCGACGCTCGCCTCCTCGATGGACAGCGAGCAGGTCGCCCGCAGCGGCTTGCCGTCCACGTCGAAGAGCGTGTACGACACCGACAGGTTCGACAGGACCCCGTCGAACGACGTCGTTCGCGCGCTGCCCCACTCGAAGCGCACCCAGGGGCTCGCCGGCTTCTTGCGGCCCAGGCTGGCCGGGGTCGGCACGCACGCCTTCATCAGCTTCTCCACCGCCTGCTCGACCGAGTTGTCGTGCTTGGCGGTGGCGTCCAGGAACACCTCCAGGCTCAGGGTGCGGGGGCCGCTGCCGACGAACTCGGGCAGCGCCGACTGGCCCGCCATCCGGGACGGGGAGCGTCGCCACTCGGTGGTCTTTCCCAGTTGCAGAGTCGAGGGGTTGAACTGCAGGTCGAGCCGGGCGATCGTCCCGCCGGGCTTGGCCCCGACGGATGCCGGGGGCTCCTTGAGGGTGAGCTGGGCCCGGGCGCGGCTGGCGCGTGCCGAAGAGGCCATGCCGTGGACTTCCTTCCGGGGCGGCGGGACGGGGACGGGGACGGGCGGGGACGCAGGGGGACGGGCAGGGGACGGGCTGGTCAGGAGGGCAGCAGCCCCTGGTGGGCGATCTCCAACGTCTCCACCGCCGCCGCGGAGTTGGCGGGATCGAAGGACGGGCCCTGCCAGCGCACCGGGACGATCCCGAACACCTGCCAGCCGATGATCCGGCTCAGGTCGGGCCGCAGCGCCACGATCTCGCCGTCCTTCGGCTCGACCCGGCGCAGCGTCTCGTCCAGCCAGCGGCCGATCTTCGCCGTGTCCGTGGTGACGGGCCGGGTCAGCGTGATGTTCGACCAGGTCACACGGCCGGGCAGCTGCCAGGTGAAGCCGTTGTTGCCGCCCTCGGCGTAGCTCTCCATCTCGACCTCGGCGCCCATGCCCGAGCAGGTGTGGAAGGCGCCCAGGTCGTTGCCGCCGATCGCCAGCCGGAAGAACACGCTGGTCGCGAAGATGTTGTCCGTCATCGGTCCGTCGTCGTCCGTTTCTCGTTCGTACGTGTTCTCAGCGGCGCCCGTCGAAGGGCCTGCCCGCGCGTTCCCGGCCGCGCCGCAACTCGGTGCGCAGGAGGCGCGCGACCGGGTCGAGCAGCCGCCGCGCCAGGTCGTCCAGGTCGAGGTCGCCGCCGCCGTGGGCCGCGGCGTCGCGCCCGCCGCCGGCCCGGCCGGCCCGGCCCGTGTCGCGCTGTACGGGCGGTGGCGGGCCGCTCGGCGGCGGTACGGGGACGGGCGGGCCGGCGAGGGGCGGGCCCGGGACGGCGGCGGGAGCCGACGCCCGGGGGCGCACGACGGGTACGGATCCGGCGGCGGGGGCGGCGGGGGCCGGCTGGACCACGAGCGGTGGCGTGTACGGGCCGGTCACCGGCAGAGGTGCAGCCGCCGTGGCGGCGGCCGCGGCCGACGCGGGCGCGGGGCGCACGGCGCGCGCGGGCCGCGGGACGGGGGCGGGCGCGGCGGGCGCGGAGGCTCGTTGGACCGGCTGCGGTGCGGCGGCCGAGGGCGCGGACCAGCGTGCGGGGACCACGGGCCGGCGGGCCGGGCGGGAGGCGGCGGGCGTGCTGCCCAGGCCCGCCGCGTCACCGGTGCCGAGGGCCAGGGGCCGCGCCGCCAGCAGCTGGAGGGACGGGGGCGCGGCCGGCGCGGCGGCCGCCGCGCCGCCGACGGCGCGGGCGGCGACGAGCGGGACCGGTCCCGAACTCCGGGGGGCGGTGGCCCGCTGGACCGGCGGGGCGGCGGCCCGGGGGTGTGCCCCGCCCGCCGCGCCGCCCAGCAGGGGCGCCTGCGGCCGGGCGGCGGCCGGCCGGGGCACGGCGGCGCTCGTCGGCAGCGAGGGCAGGGGCGCCCCCAGCCCCGAACGCACGCGCGGCGCGACCCGCCCCACGGGCCCGCTCGCCGCGGGCTCGGCGGTGGGTATGGCGGGTGCTGCCGGGCTGCTGGTGGTGTGCTCCGTCTGGCGTTGCACGGTGGGCATGGCGGGGCCCGGGGTGGCCGGTGCGGGGTTGGACGGTGTGGCGGTGGGCGGGAGTTCGGTCAGGGGGGCGCCGAGCGGGGCGCGGGTGCGCATCGGCTTGTCGGCCGTCGGCCCGCTCGCGGCGGTTTCGGCCTGCCGCTGCACGGTGGGTATGGCCGGTGCTGCCGGGCTGGTGGTGGCGGGTTCGGCCGCGCGCTGCACGGTGGGCATGGCGGGGCCCGGGGTGGCCGGTGCGGGGTGGGACGGTGTGGCGGTGGGCGGGAGTTCGGTCAGGGGGGCGCCGAGTGGGGCGCGGGTGCGCATCGGCTTCTCGGGCGTCGGCCCGCTGGCGGCGGGTTCGGCCTGCCGCTGCACGGTGGGCGTGGCGGGTGCTGCCGGGCTGGTGGTGGCGTGCTCCGTCTGGCGTTGCACGGTGGGCATGGCGGGGCCCGGGGTGGCCGGTGCGGGGTGGGACGGTGTTGCGGTGGGCGGGAGTTCGGTCAGGGGGCGGCCGAGTGGGGCGCGGGTGCGCATCGGCTTCTCGGCCGTCGGCCCGCTCGCGGCGGTTTCGCCCTGGCGCTGCACAGTCGGCATGGCCGGGCCGGTGGGCGAGGGTTCGGCCGCGCGCTGCACGGTGGGCTTGGCCGGGCCCGGGGTGGCCGGTGCAGGGTGGGACGGCGTCGCGGGGGGCGGGGTGCCGAGCGGGGCGCGGGTGCGCATCGGCTTCTCGGCCGCGGGGCCGCTCGCCTCTGCCTGCCGCTGCACGGTGGGTATGGCCGGGGTTGCCGGGCCGGCGGTCGGGGGTTCGGCCTGGCGCTGCACGGTGGGCATGGCGGGGCCCGGGCTGGCCGGTGCGGGGTGGGACGGGGACGGTGTGGCGGGGGAGGGGAGTTCGGTCAGGGGGGTGCCGAGCGGGGCGCGGGTGCGCAGCGGGTTCTCGGCCGTCGGCCCGCTCGCCGCGGACTCTGCCTGCCGCTGCACCATCGGCATGGGCGCGGCGGCCGTAGGGCCGGGCGGTGTCGAGGGGGCGGCCGGGGGCGGGAGTTCGGTGGGCGGGGCGCCGAGCGGGGCGCGGGTCTGCGCACGCTGCACCGGCAGGTCCGGGCCGGCCGCCGGCAGGGCGGGGGGACGGACAGCCGCCACACGGCGGCGGGGTGTCGCAGGGACCCGCGCGGTGGTGAGCGTACGCCCGACCGGGCGCGGCCGGACCGCGGTGGTGCGGTCCGCGCCGGGCGTCTCCCCGGACGTACGAGCCGGCCGGGCGTCCGCGGCCGCCCGTACGGGAGCGGAGCCGTCGGCGGCAGGAGGCGCGGGGATCACCGCGATACGCCGGACCACCGGGAACGCTGCGGGTGCCGTCGCGCGGCCGGGCTCGGCGGCCCGCTGCACGGGCGGCGCGGACGCCCCGAGCACGGCCGGGGAGTCCGTGGACGTGAGGCCCCGCGTCCCGGCCGCGGCCATGGAGCCGGAGCCCTGCGTCCGGGTCCGGTTCCGGGCGCGAGCCGGTGACGCGCTGTTCGCCGCAGAGGCGGAGGCGGCGGACGTGCTCGACGCGCCACGGGCCTCGGCCCGCGATCCGGCCGGGCCCGGTGTGCCGGCGTCCGCGCCCCGGTCCGCGGTCGGCGCGGTGGCGCCGGGACGGGCCCGGCGCGAGACCTGCGGGGTTTCGCGTGCGGGCCCGGCCTGTTCCGGCTGCTGGTCCGCGCCGGTGCCGGTGGGTTCGCCGGGCAGCGCCCGCAGCAGCAGCGGCCCGCCGCCGCTGTGGGTGGGGCGGGCGGTGGCGGGGCGGGCGACCCCGCGGACGAGTCCGGCCGGGGCGGACGGCAGCAGCCCGTGGGCGAGTCCCGTGTCGAACGACGGGTTGCGCCACGCGGCCAGGCCGGAGCGGAAGGCGAGCCCGTCGCTGACCCCCGTGACCGACCGCGAGACGGTCAGCAGCGGCGGCGCGGTCATGCGCCAGCCGCCGTCCCAGTCGCCGGGTACGGCGGGGCCGGCGGCCGGCACGGCAGCGCCGTCCGCCGCCGCCGCAGCCGGCGCCGAGGCCCCGGCATCCGGCACAGCGGTGCGCCGCCGCAGCCTGTCCCGCCATGCCATCTGCTCAACCGCCTTCGTTCACACGGGTGTTGATCCGAGCTATCTCGGTGACCCAGTCCTGGCGCTCGCCATGGGTCAGGTCGAGGATCTCGTCGCGCCGCCAGTGGAAGTGGTAGGCGATGTACGCGATCTCCTCCCGGAGCCGGGGGAGCGCGTACGTCACGATTCCCCCAGGCGCCCACCGGAGAGGTCGACCTCGAAGCCGCCGTCGCAGTGCGGGCAGGTGACCGCCGCGCGGGTGTGGCCCTCGCTGTTGACGCGCCGGTAGAAGTCCTGGAGGAACGCGACGTCGGTCGCGTACATCCGCTCGACGACCCCGGCGTGCACGTCGGTGATGGTGCCGAGCCTGGTGATCACCTGGCTCAGCAGCACCACGCTCAGGTACGCCGGGTTCTCCTTGACCCGCAGGTCGATCTGCGGGCGGAGCTCGTCGCGCGCGGTGGCCAGGCGCATCGAGCCGTGCCGGTGCACCGTGCCCGCCTCGTCCACGTAGCCGCGCGGCAGCTCGAACTCGTACTCCGTGCGCAGCCCGTGGTCCTCACGGGGGCGCGGAGCGGCGGCGGCCGGGGCGGCCGCCGCCTGCTCCGGGGCCTGGGCGGGCGCCGTGACCTGGAGGATCTCCTCCAGGCTGCCCGCGGTCACCGTGCGGCGCCTCATTCGACGATGATCTCCTCGAACACGATGGTCACGGACTCGGTGGCCGCGGCGGACTCGCCGGCCTTGAGGGAGGGGCCCTCCCACTTGGACGCCCAGCCCTGCATCAGCTGGATGCGGCGGATGGTCGCGCCAGTGGAGTCCTTGATCTCGATCGTGAGGTTCTGCCGCGCGGTGTCGACGGCGCCGTTGTTCAGCGTCTCCTTGATCCACTTGGTGAACTCGCTGCTCTTGTCGAGTCCCCGGGTGATCGTGACCTCGCCCGCCTGGCGCGCACCGGGCTGCTTGCGGATGATCTGCTTGCCCTCCGCGCTGACCTGGCGTACCTCGACGACCTCTTCCTCGACGGTCAGGCCGCTGATCTCCTGGATGGATTCGACCAGGTAGCCGCCGAGCTGAACGCCGAAGATATGGGTGGAAAGAGCATCGCCCTCTGCCATGACTGTCCTTCACCTTTCCTTGCTGCTGCCGGTACTGGCGGTGCCGCTGCCCCGGAGGGTCACTCGTCGACGAGGCTGGTGCTGTCGGAGAACTGGGCCAGCCGGAACACCACGAACTCGGCAGGCTTGACGGGCGACACGCCGATCTCGCAGACCACGCGGCCCTGGTCGATCGACTCCTGCGGGTTGTTGTCCCGGTCGCACTTGACGTAGAACGCCTCCGCCGCCGTGCGGCCGAACAGCGCGCCGCGGCGCCACTCCTCGGTCAGGAACGCGGTGACGTTACGCCGGATGCTGGACCAGAGCCGGTCGTCGTTCGGCTCGAAGACCACCCACTGGGTGCCCAGGAGGATGGACTCCTCCAGGTAGTTGAAGAGGCGGCGCACGTTCAGGTAGCGCCAGGCCGGGTCGGAGGAGAGGGTGCGCGCACCCCAGATCCGGATACCGCGACCGGGGAAGGCCCGTACGCAGTTCACGCCGATCGGGTTGAGCAGGTCCTGCTCGCCCTTGCTCAGGCGCAACTCCAGGTCCACCGCCCCGCGGATGACCTCGTTGGCGGGGGCCTTGTGCACTCCGCGCTCGGCGTCGCTGCGCGCCCAGACGCCGGCGACGTGGCCGCTCGGCGGGACGGTCGTGTTGCGGCCCGACGCGGGGTCGAAGACCTTCACCCACGGGTAGTAGAGGGTGGCGTAGCGGGAGTCGTAGCCCGCCTCGTCGTTGCGCCAGGTGCGCACCTGCTGCGCGGACAGCGCGGGCGGGGTGTCCAGCACGGCCACCCGGTCGCCCATCTGCTCGCAGTGGGAGATCACCGCGAGCTGTACGGTGCGCACGCCCTCGGCGTCGATGTCGCCGCGCTCGTAGGCGCTCATCAGGTCCGGGACCGCGACCATGGTGATCTCGTCGATGGTCTCCAGGCCGGCGAAGCCGGTGCGGGCGCCCGCGTCGCCGACGTACTCGGCCGGGTCGAGGCGGGCCACGGCGCCCTGGCCGGTCGTGGCGGCCACGGCGGCCGGGGCGTCGGGCAGGGCCACGGTCTGGCCGGCGGGCCGGGTCTGGGTGGCGGACCGCTGCTCGGTGACCTCGATCAGCTTCGAGGCGCGCGCCTGGGTGACGAGGTAGCCCTTGACGTTCTTGCGGGAGGAGGCCTCGTAGGTCTCGGCGATCTGCTCGCCCTGGCGGACCAGGAGCTTGAAGCGGTCCTCCGGCGGGTTGTCCCCGTCGGCGTCGGCGATCTCCACGGACACGCCCGTGATGCCCGGGCGCGCCGTGATCAGGAAGCCGCCGAGCTCGACGGGCTGCGCGGTCCGGGGCTGGGGGACCGCTCCCGCGGCGGCCGGCGCTGAGCCGTCCGCGGCCGGCCCGCCGATGCGGACGACGTACGCGGCGCCGCCGCCGTTGGCGAAGTAGCCGTAGACGGCGTGGGGCAGGTAGGTGCCCTCGGTGAAGCCGCCGAAGTGCTGGGAGTACTGGTCCCAGTTGGTGACCAGCGTCGGTTCGTGGAAGGGCCCGCTCTGGGCGAACCCGACGAACGCGGCGACGGCGGTGCCGACCCCTTCGATCGGGCGAGCACCGGACTGCACCTCCTCCACGTACACGCCCGGGGTGAGGTACGTCGGCATGCTCGCTCCTTCGTCACGGCTTGCAATCAGGTCTGGTCACAGCCTTCCGCGCGGCAGCCGGCCCAGGCAGGGGAATTCGATCCTGGTCAGGGGCAGATGCGCTGCCCTCCGGGGCATCGCCACCGGGCCGTCCAGGCAGCCGGACCGCCCGTCCCGAACCGGCGCGCCCGTCCGGAGCCGGCCCGCCCGTACGTCCCGAACCGGCGCGCCCGGTCGTCCGGACCGGTCGTCCGGACGGCCGGGCCGGTCACACGTCCGCGACCTGGCCCAGGTACGGCCCGAACTCGCCTTCCAGGACCAGCCGTCCGAGCTTGCGGTACTCCTGCGCGACGGCCGTCATCACCTGGCGCATGGTCAGCGGCTCACCGGAGGCCGCCGCGAAGTAGGCGGCCGTCACCGCGCAGGCCCGGATGGAGCCCCCGGCCAGTTCGAACCGGTCGGCGCAGAAGGCGAGATCGACGTCGTCGGCGCGGGGCAGCCGGCCGCCCAGGCAGCGTTCCCACAGGGCCCGGCGCTGGGCGGCGTCGGGGACGGGGAAGTCCGCGATCACGTCGAGGCGGCGGGTGAACGCCTCGTCGAGATTGGCCCGCAGATTCGTGGTCAGGATGGCGATGCCGTCGAAGGACTCCATCCGCTGGAGCAGGTACGCCGACTCCATGTTGGCGTGCTTGTCGTGGGAGTCCTTCACGTCCGAGCGCTTCCCGAAGATCGCGTCGGCCTCGTCGAAGAGCAGCACCGCGTTGACGGCCGACGCCTCGGTGAAGATCCGTTCCAGGTTCTTCTCGGTCTCCCCGACGTACTTGTCGACGACCGTGGACAGATCCACCACGTACAGGTCCATGCCCAGGTCGGCGGCGACCACCTCGGCGGACATGGTCTTGCCGGTGCCGGAGGAGCCGGCGAACAGTGCGATCACCCCGCGCCCGCGCCCGCCGCCGGGCCGCATGCCCCACTGACCGAGCACCTGGTCGCGGTGGCGTGCGCGTACCGCGAGGTCGCGCAGCCGGCGGTGGGTGGGGGCGGGCAGCACCAGGTCGTCCCAGCCCACGGCCGGCTCCACACGGCGGGCGAGGCGGGCCAGGCCCGCGCCGTTCTGCGCCCGTACGGCGGATCGCAGGTCGTCGGGGGAGACGGGGCGGCCGTCGAGGGCCGCGGTACGCGACGCGGTGTCGGCGGCGCGCCGCAGCTGGCCGGCGTCGAGGCGGTGCGCGGAAACGGACCGGGCGAGCGCCTCCGCCCTGCCGGCCTCCGCACCGTCCGCCTCCGCCCGGCCCGCGCCCCCCTCCATGCCTGTGCCGGCTGCCCCGTCCGTACGGCCGTGTTCGGCGGCGGCCCGTTCCAGGGCGTGCCGCCAGCGCACGGCCTGCCGGTCGGGGGAGGGCGCCGCCACCGTCAGGCAGACGGGGGTGGCGGCCGCCCAGGCGGGCTCCCACCCGCTCGTGCCGTGCGTGAACAGGGGGATGCCGCGCAGCACCGTGCACAGGGTGCGCAGTACGTGGGCCCGCTCGTCGGGCTTGTCGGGCAGTGCCTCCAGCGGTCCGAGCAGCACACCGGCGCCCAGCAGCCGGGCTTCGCGGGCGGCGGCGCGGGCGAGCGCGGGCAGGGCGTGGGCGCGGTGGGTCAGCGCCGCCGGGTCCAGGACCAGGGGGCGCAGCCCGCGGGCCCGCAGTGCGGCGGCGGCCAGGCCCTCGGGGTCGCCGCCGCGGGTGCGCAGGTGGACGTGGCCGGTGCCGTTTCCGGCCGCGGCGGCGGCCCGGTGCAGTTCGCCGGGGTCGACGGCCGGATCGTCGGCGGCTTCGCCGAGCACCTCGGCCAGGTGCGGATCGGGTGCGGCGGCGCCGAGGAGGTGGGCGGTGACCCGGTCCGGGACGGCCAGCACCCGGGACAGGGGCGGCCGGTCGGGCTCGGTGACCTCCAGCAGGCCTCCCGCTACGAGCGGTGCGCCGGGGGAGAGGCGGAAGCGGGCGGCGGCGGACCGGGCGCGGCCGCACAGTTCGAGGGCGAGTCCCACCGTCGGCCGGCGGCGCGTCAGGTCGTCGTTGAGGTAGCCGTAGAGCCGCTCGAACCGGGCGTCCAGGTCCGGGGCGAGTGCGACCAGCAGCAGGTCCACGTCCAGGGGCTCCAGCGCGAACCGCGTGGCGAGGACGCCGAGCGGCGAGCCGGGCGGCGGAGGCCAGGCCGGCGCGAGGGCGGGCAGGCCGGGGCCGTGCTCCCCGCCCTCGTCCAGGATCCGGGCGACCGCCTCGGGCGTGAGGTACTGGCCCCGGTAGGGGTCGTCCGGGTCGGGGTCGGCGGCGCGGCGGAGTTCCACGGCCAGCCGGACCCGTTCCTCGACGAGCCGGAGCCGCGCCCACAGGTACGGGACCCCGTCGCCGCGGTCCGCGACCCGGTCCGCGTCCCGGTCCGCGTCCCGGTCCGCGTCCCGGTCCGCGTCCCGGTCCGCGACCCGGTCCGTGTCCCCGTCCCGGGGCCGGTCCGCGTCCCGGTCGGGAGCGGGTTCCTGGACCAGGGCCTGCTCCCGGTCGTCCACCGGGGGCTGGAGGGTGTGCGTCACGGCTGGCGTTCTCCTCGTCGGCGCCGGGCGGGAGCCTTGGGCCGTTCCCGGGAGCCGCCGAAGCCTTCCGGTCCCGGCGTGCCCAGTTCGACGTAGCGCAGTCGGCGCGGGCTCCCGTCCCCGTCCGGCCCGGCCTGCGGTACGGAGTTCACGACGAGGCCTTGGGTGACCGGCGGTGCGGTGACCTTGCTGATGCCGGCCAGCGGGGCCTTCACGCGCAGCCCGAGGGACGGCTTCAGTTCGCCGCCCAGCGCCGACCACACGTCGGAGGCGGCCGGCGCGTCCATGCCGGTGCCGCCCGCGTCCACGTCCACGAGCAGGCCGAGGTCGGCGAGCGTCCCGGTGAGCAGGCGCGGGGGCAGCGTGTCGGTGGCGACGAGGCAGGAGAGCACCTGGGACAGCAGCCGGTGCTCGTCCTGCGGCCTGCTCGCCCAGGCGGTGACCAGGTACGTCAGCTCGAACCAGCGCGGCGGGGTGCGGCGCGCGACGACAAACCCGTCCTCGTCGAACACCTCGCCCCCGCCGCTGCCGCGCCGGGTCGGATCCTCCCTGATGTCGTAGAGGAACACGCAGACGGTGGGCGCGCTGCGGCGGGCGGCCCAGTCGCGGGTCGGCGCGTCGAAGACGACCTCGACGCCCGACGCCTCCAGACCGGATTCGGCGAGCAGCCGCCGCAGCCCTTCGTCGACCTCGTGGATCACCGGCGGGTCACCTCGTCGGGCGGCTGCACCGTGCCGTTGACCACGAGGAAGTCGGTCTGCACGGGGGAGAAGCCGGGGCCGCTCGCGGTGATGATGCGCGGGCCGGTCTGGTCCTTGGCCAGGATCAGCAGCTGGCCGATGAACGTGCCGTCGGCCTGCGGGACGGTCGGTGCCGCCGCGGCCGTGATGCCCGGCTTCCACGCGAACCGCACCGGCGCGCCGGGCGGGAAGTCCTCGCCGCGTACCGAGGTGACGAAGCCGGGCCTGCCGATCGGCGGGACGGCGACGATGCGCGGCTGGAGGATGCGCAGCTGCTCCCGGGCGGTGTTGTCGCCGGGGTCGGCGTCCGTGCCGGTCGTCGTGAGGTTCGCGGTGACCTGGCCGGTGAGCGCCTTGTCGGGGCTGAGGACGACGCGCAGGACGGTGCGGGCGCCCGGTGCGAGGTCGGCCAGCGCGCACGTCCAGTTCCGGTCGCAGCCCGGCGGCGGCCCGTCGTGGGGGACGCCCTCGGGCAGGCCGATGCGCAGCCGCAGTCCGGTGGCCAGGGCGCTGCGGCCGTTGGCGACGGTGAAGGTGACGACGACGCGGCCGCCGACGTAGCCGGGGTTCGGCTGCGCGGTGATGCCCACCCCGGGGCCGGCCTGGGGCGCGGGCGGCTGCGGTGCGGGAGGGGGCGTCGTGGGCGGGGTCGTGGGCGGGGCCGGCGTCGGGGTGGGCGGTGTCGGCGTCGGCGTCGGCTTCGGGGGTACGGGGGCCTCGCGCACCGGCACCACGGTCCGGCCGGCGTTGTCGCTGGGGCGGGGGTCGAGGACCGTGCCGGTGACCGACCACTCCACGGGCTGGTCGCCGGGGATGAGCCCGGTGAGGGTGGCGGTCACCGGGACGGTGGTGCCGGGCGGCACGATGCCCAGGGTGCAGGTCAGCGCGGCGGCGTCGCAGGTGGCGCCGGGCGTGCCGGGCACGGTGAGCGCGGTGATGCCGACGCCGAGCGGGGGTGCGACGGTCAGGCGGGTGCCGGGGGAGGCCGCCGGGCCCTGGTTGACGACGTCGACCCGGACGGTGGCGGAGCCGCCGACGGTGAGCGGCGCGCTCTTGTCGGGCGCGCGCACCGCGAGGTCCACCGACTGCTGCACGCTCGGTTCCTTCTGGCGGCCCGGCAGGCCGGTGACGAGCAGGTTGTGGGCGCCGGTCGCGACGTCCACCAGCTTCAGCTTCTCCGGGCTGTTGGCGGCCCGGGAGCCGCGGCCGGTGAGCACCAGGGACTTGCCGTCGGCGGTCCAGGCGGCGTCGCGGGGCTGGTAGGGGCCGTTGCCGGTGGTCTCGGGCAGCTCCCGGCCGCAGGCCCCCGGCTTGCCGCGGGCGGCGTCGGGCAGCAGGACCCGGCAGGAGCCGCCCGCCGGGGAGGCGAGCAGGATGCCGCTGCGCTCGTCGACGCGGCCGGCGCCGTTCTTGCGGTTGAAGGCGACGGTGGTGCCGTCCGGGGAGAACGCCGGGCTGTCGTCGATGACTTCGCAGGCACCGAAGCAGATCGTGGCACTCAGGTCGCGCTGCCGGTCGAGGTGGTCCACGGGCACGGTCCAGATGTGCTTGTTGCCGCCGTGGCCGTTGATCACCAGGTTGCGGGTGAAGGCCAGCATCGTGCCGTCGGAGGACCAGGTGGGCTGGGCGTCACCGCCCTTGGGCTGGTCCGCGGGCGGGGTGATCTCGCCGCGGATCGCCCCGGTCGCCGCGTCCGCGATCAGGATGCGGCTGGGGCCGGCGGCCTGGCCGACGCCGCCGGGCGAGGTCCGGGTGAAGGCGAGGTACCTGCCGTCGGGGGAGAACGTCGGGTCGGTGTCCCAGTCCTTGGGGCCGCGGCCGGCGAGCGGCAGGGCCTCGGCGTTGGTGCCGTCGGCGTCCGCCGTCCAGATCCGCTGGATCCGGCTGCCGGGCTTGCCCTCGAAGCGGGTCACCACGATCCTGCGCCCGTCGGGCGTGTAGTTCTGCCGCTCCGTCCACGGGTCGAAGTCGGGTCCGGGTTGGAACAGCGGATCCTTGGCCGGGTCGGTGTTGGTGTCGGCCGCCGGGTCCTCGTCGAGGATCGTCAGGCCCAGGTCGCGGGGGTCGGAGCCGTCCATCCGCGCGTCCTGCAAGGTCACCACGTGCGGGCCGGCCGCCGAGATCCGCTCGACGACGGCGCCGCCGCCCTTGAGGGGGCCGAGCCAGGTGGGCGAGCCGATTTCGCGGTCCTCGCTGTACACGAGCTTGGGGGTGTCCGCCGAGTGCGCGGGCACCTGGAACACGTGGTCCCAGTCGCCCTTGCAGTCACAGGTGCGGTCGGGGCTGAGGAAGAGCAGACCGTCCCCGTCGGGCAGCCACGCTGCCCCCCGGGTCCGCCAGCCGGCCTGGGCGCCGGCCAGCAGCTGCCCGTCGGCGCGCCCGTTCGTCCACCGCAGGCGGGGCCCGGAGGCCCCGGTGGCGGTGTAGGCGATCACGTCGCGGTTCGTCGCGTCGTCGACCGGATTCCACACCGGTTCGGTGGCCCGGCCGTTCGCCGGGTCGGTGAGCCGGGTGGCGGCCCCGCCGCGCAGGGGGCGTACGTAGACCTGCGCTCCGGCGGCCCGGTCGGCGTCGGAGGAGTACGCCAGGCGCCCGCCGTCCGCGGAGACCGTCGGGTGCTCCTCGTTGGCGGGGGTGTCGGTCAGCCGGGTCAGGCCGGTGCCGTCGGTGCGTACGAGCCACAGGTCGCGCTGGACGCCGCCGGCCGCGCCGCGCTGGGCGGAGTCGAAGACGACCGACCGCCCGTCGGGGGTCAGCCGAGGGTTCCCCGCGTCCATGCCGCTGGTCAGCCGCCGTACGGAGCCGTCCGCGGACCGCAGGTAGACCTGCGGGTTCTTCTCGTCGCGGCGGCTCGCGAAGACGAGCAGGTCGCCGAGTGCCGACGGCTGGACGTCCAGGTGGGCCGGCCCGTCGCCGAACAGGGGGGTGCTGGTGTCGTTCTTGTCGTTCGCCACCCGCCCCAGGCTGCGGTGGCGCGTACCGGCGTACGCGACCCTGCTGCTCCCGGCGTCGGCCGCGAGGGGCTGCGCCCCGGCGTCGCCCGGTCCGGCGGCCGCCGTCACCGCGAGCAGGGGCGCCAGCAGCAGCATCGACGCGCCGGCCCTCCCCCAGCGGTGTCGGCGACGGCCGGACCCCTCCGTGCCCCTCACGGCCCACCTCACAGTCCGGTCCCGCATCCTGCCTGTCACCCCGCCACCCTGCCGGTCCGGCCGCGCGGACCGGCAGGGCCGCGGGGCCGGACCCGGGGGAAGCGTCCCTTGCGCTTTCGGGCAGCGGCGGCCGGTCGGAGCCGTGCGGGCTGCCGTGTGCGGTCAGATCAGCCCGTTGCGCAGGGCGTAGCCGACCGCGTGCGTCCGATTGCGCAGTTGCAGGCGCGTGATGACCTCGTGCAGGACGTTCTTGACGGTCCGTTCGGAGTAGGAGGTCTTGCGTGCGATCTCCGCGGTGTCCAGGCCCTCCGACACCAGCCGCAGCATGTCCGCCTCGCGCGAGGTCAGGGTGGACAGGGACACCGAGCGCGGGTCGAGCGCGGAGCGCTGCAGGCTTCCCATGTGGTCGAGGAGTTTCGCGAGCAGGTCGCCGGGCAGCACGCCCTCGCCGTTCGCGATCGCCAGGACCAGCCGCAGGAGCCGGTCCTGGTCGGCCTCGGCGCGCCGCAGCACCGCGCTGACCCCGCATTCGATGGCGCGCTGCAGGGCGTCCCCGGACTCGAAGGTGCCCACCACGAGGCCGGTGCGGGTGTCGGGGTTGTGGCGCAGCCGGTAGAGCAGGGCGGCCGTCTCGTCGTCGACGCTGTCCACCGTCACGAGCGACACCTGCGCGGCGTCGGCCTCCGCGTCGGGGACGAGCTCGATCTCGGGGCGTTGGCGCAGCTGGTGGACGACCCCGACGCGCAGGATCGGGTCCGACGCGTACACGGCCACCGTCACCCGCCGGCCCGTTCTGCGGGGAGGGGCCGGGGCGGGGGGCTGGGGTATGCCGGAGCCGGCGTTGAGGGAGGGGCTGTTGTTGTCAGCGCAGCGCATGTGTCGTACCTGTTCCGTGATGCGTATCTGGGGTGACGGATCGGCCGGCCTGGTCGGATCGCGACGTTGAGATCCAACCGGCGGCCGTGCATGAGGAGTTGGGGAAGTCTGTGGGGGCATCGGGACTGCCCGGGGCCTTGCCCCCGCGTCCGTGGTGGCGGCCGGGGCGGCGCCGTAGCGTCGTGGCGTGACATCCCCAGCTGCCTCTCCCAGCCCTGGCGCGCCCGTCCTCGACATCGAGCCGGTGTCGGTGATGCCGGGCGGTACCGCCACCACGAGCCTGACCGTGCGCAACGACAGCGACATCGTCGAGGCGTACCGCCTGGAAGTCGTCGGCGACTGCGCTGCCTGGACCACGGTGGAACCCGCGCGCGTCTCGCTGTATCCGGGAACCTCCGAAACGGTCACGATCCGACTGGCGCCGCCCCGTTCGCCCCAGGTGCGGGCCGGGGACGTGCCGCTCGCCGTGCGGGTGCTGCCCACCGAGCAGCCCGATGCGGTGCGGGTCCCCGAGACCACCGTGCATGTGGAGCAGTTCCGGGAACTGCGGGCGGAGAGCGCTCCCAAACGCCGCCGCGGATGGCTGCGCGGTCGTTACCGCATCGCCGTGCGCAACGAGGGGAACGCCCCGGTGAAGGTGGGCTTCACGCCCGCGCAGCCGGGCGAGGAGCTGAAGTTCGACTTCGCCCCGCCCACGCTGAAGCTGGAGCCGGGCGAGTCCGCCGAGGTGGTGCTGAAGGTCCGCGCCGCCGGCCCGGTGTGGTTCGGGGCGCCTGTGACCTGGCCGTTCACCGTGGAGGTGGCCGAGACCGCGGAAGGCGGCGACGGCGAGGACGCCGCGGCGCGTGCCGAGCATGAGGCCGTACGGGGGCCGCTGGAGGTGGAGTTCGTCCAGATCCCGATCTTCCCGACGTGGCTGCTCGCGGTGCTGGCCGCACTGCTCGCGCTGCTGCTCGCCTGGTTCATGCTGGTGCGCCCGGCCGTGCGCAGCACGGCCAAGGAGGCCGCGGCCGAGGCCGCCAGGAACCCGGCGCCCGCCGCGGACGCTGCGGGGCAGACCCCGGTGACCGGTGGCGGCAAGCAGCCCGGCGGCGCGGGTGCGGGACCGGGCGCGGCCAAGGGCAACCAGCCCGGGGCGGGCGGCGGCGGTTCGGGTACCGGAGCCGGCGGCGGCGGGGGAGGGCTGCAGAGCTCGGCCACCATCGACCTGCAGACCGGCGGCGGTCAGAGCAAGACCGGCTCGTACACGGTGCCCGCGGGCAAGGTGTTCGGGATCACGGACATCGTGGTCGCCAACTTCCAGGGCGACGAGGGCGTGGTGACGATCAACTTCGGCGATCGGAAGATCACGACGATTGCGCTGGAGACGTTCCGAAACCAGGACTACCACTGGGTCACCCCCATCAGCATCACCGAGAGCCAGACTGTGACCGTGCAGGTGACCTGTGCAAAGCCGGGCACGCCGGCCACCGGCCGTCAGGCGCAGGAGTGCCACGAAGTCCTCAACGTGAGTGGTGTGCTGAGCGACCTCAGGTGACCCGAGCGGCACGGACATCGTCCGTCAGGCTCGGCCAGGAACAAAGCGGACCCGCACCGGTCCGTCCGGAAAGCGCTTACCGGACGGGCTGGTGACGGGTCGTCGGCATTCCCGCCTTCCGGTGCGGTGACGCCGTTCCACGGCTCTTGCGCGACTACTGGGCGGTAGCAAGACCGTGGAAAAAATTTGGCTGTATTTCGCCTCTCGCGCCTCGCCTGCAACTCCCCGCTCCCTGGCCCGCCCGGGTCGCGGCAGGGGGGCAGCGGCATGTTCCGGCCAGCGCGGTGCCGCCCGGGTTCAGGCAGCGGCCGGGCTCGGGGGAGGGGAGGGAGGCGTCAGGGCCAGACCAGGCAGTACGGCTGGTGGCCGGCCTCGTGCAGCCGGTGGCTGAAGTCCTGCCACTCGTGGAGGAGCTGGTAGACGTTGAAGGCGTCGCTCGGGCCGCCGCGGTCGGGGACCGTGGACCAGATGAAGGCGGCGGCGCCCACGGACTCCTCGCCGATCCCGCGGAGCGGGTCGACCACCGTCATCGGGAGCTTGACCACCGCGTAGTCGGGGTGGAGGACGACCAGCTCCAGCGGCGGCACCTTGTGCAGGGGTATGCCCTCGATGCCGGTCAGGACCATCGCGGCCACCGTCTCCGGCTTGATCTTGGTGAAGAGGCCGCCCATGCCGAGCTCGTCGCCGCCGAGCTCCTCCGGGCGCATCGTCACCGGGACCCGGGCCGCCGTCGCGCCGTCCGGTGCGCCGAAGTACTTGTACGTCACGCCCATGCCGCGGCCCCGGGGCACGTCCTCCGGCTCCGCCGCGGGCTCCGGCACGGCGTCGGCCGCCTCGGTGGCGCGCCGGCGGTGCTTGCCCCGGCGGCGGGCCTCGCGGGCTTCGCGGGCGCGCTGCGGATCGAGGCCGTCCGTACCCTCGCCCGGTCCACCACCGCGTTGCATATCTCCACCCGACTGGTCTTGCTCGTCCCGGCCCCGTGACCTCCGCCACGCAGCCTGATCATCATGGCAGTGACCTCCCCCGCGGCGACGCGGTGAAACGCCCGCCCGCAAGTCTGTCGCAGCCTCTGAGACCATGGCTGGTGTGAGCTACCCGTACCCGTATGAAGCCCCAGTTTCGCAGACGCTCTTCGAGCGCGCCTCCCTCGTGACCCCCGGCGGCGTGAACTCTCCCGTGCGCGCCTTCCGCGCCGTGGGCGGTACGCCCCGGTTCATGGTGTCCGGCACCGGTCCGTACCTCACCGATGCCGACGGCCGCGAGTACGTGGACCTCGTCTGCTCGTGGGGGCCGATGATCCTCGGCCACTCCCACCCCGAGGTGATCGAGGCCGTCCAGGCGGCCGTCGCGCGCGGCACCTCCTTCGGTACGCCCGGTGAGGGCGAGGTGGCGCTCGCGGAGGAGATCGTGGCGCGCATCGAGCCGGTGGAGCAGGTGCGCCTGGTGTCCTCCGGGACCGAGGCGACCATGTCGGCGATCCGGCTGGCACGCGGCTTCACCGGTCGCGCCAAGGTCGTGAAGTTCGCCGGCTGCTACCACGGTCACGTGGACGCGCTGCTGGCCGCCGCCGGTTCCGGGCTCGCCACCTTCGCGCTGCCGGACACCCCCGGCGTGACGGGCGCGCAGGCCGGCGACACGATCGTGCTGCCGTACAACGACCTCGAAGCGGTGCGGGCGGCGTTCGCCGCGCACCCCGGCGAGATCGCCTGCGTGATCACCGAGGCGGCGCCCGGCAACATGGGCGTGGTCACCCCCGCCGAGGGCTTCAACCAGGGGCTCGCGGACCTCTGCCGGGAGAACGGCGCGCTCTACATCTCCGACGAGGTCATGACGGGCTTCCGCACCTCCCGCGCCGGCTGGTACGGCGTCGACGGGGTCAAGCCCGACCTGATGACCTTCGGCAAGGTCATGGGCGGCGGCTTCCCCGCCGCGGCGTTCGGCGGCCGCGCCGACGTCATGGGCCACCTCGCCCCCGCGGGGCCCGTCTACCAGGCCGGCACGCTCTCCGGGAACCCGATCGCCACCGCCGCGGGCCTCGCGCAGCTGCGGCTGCTCGACGCGGCCGCGTACGAGAAGGTCGACGCCGTCTCGGCGGAGATCCAGGGCCTGGTCACCGGGGCGCTCGCCAAGGAGGGCGTGGCGCACCGCCTGCAGACCGCGTCCAACATGTTCTCCGTCTTCTTCACCGGGGACGCGGTGCGCAACTACGACGACGCGAAGAAGCAGGAGAGCTTCCGCTTCAACGCGTTCTTCCACTCGATGCTGGCGCAGGGCGTCTACCTGCCGCCGTCCGCCTTCGAGTCCTGGTTCGTGTCCACCGCCCACGACGAGAAGGCGATCGAGCGCGTCGCGGCAGCCCTGCCGGCCGCCGCCCGGGCCGCCGCGGAGGCCACCGCATGAGCGCCGTCGGCCGCGACGCGAAGTCCGACCTCACGGTCGTGCACCTGGTGCGCCACGGTGAGGTGCACAACCCGGACGGGGTCCTGTACGGGCGCCGCGAGGGCTACCACCTCTCGGAGCTGGGCCGCCGGATGGCGGACCGGGTCGCCGAGCACCTGAAGGGCCGGGACATCGCCTACGTGGTGTCCTCGCCGCTGGAGCGGGCGCAGGAGACGGCGGAGCCGATCGCCAAGGCCCACGGGCTGGACCTGGCGACGGACTCGCGGCTGCTGGAGGCGGAGAACGTCTTCGAGGGCAAGACCTTCGGCGTCGGCGACGGCGCGCTGCGCAGGCCCGGCAACTGGAAGCACCTGACGAATCCGTTCAAGCCGTCCTGGGGCGAGCCGTACGTCGAGCAGGTGGTCCGGATGATGAGCGCGCTGGAGGCGGCGCGCGACGCGGCCCGCGGCCACGAGGCGGTGGCGGTCAGCCATCAGCTGCCGATCTGGATCGTGCGCAGCTTCGCCGAGAAGCGCCGGCTGTGGCACGACCCGCGCCGCCGGCAGTGCACCCTCGCGTCCCTGACGTCCTTCACGTTCCAGGGCGACAAGCTGGTGTCGGTGGGCTACAGCGAGCCGGCGCGGGACCTGGTCCCGGCCCACCTGCTGGCGGGGGCGAAGCCGGTGAAGGGCGCCTCCAAGGCGTTCGGCGCCTGATCCGACGGTCTGTTACGGACCGTTACAAGCCTGTCTAACTAAATACAAGATGCGCGGGAATCACCGTGTCAGCACACATGTCCGGTCAACTTGTCCGTTCATGCGGACTTTGAGTCGGGTGTGGTGACGACGATGGGGACGGTGACATGCGCGACATCAGGGGAGTCAGTCGGAGGGGGTTGCTGGGACTGGGACTTGGCGCCGCGGCCGCGATGGGAGTCGCCGGCTGCGGACTGCCCGATGTGTCCGGTCCCGGCGCTCCCGGACCCGTGAAGAACCCGAAGCCCGGTGAGAAGACGCCGGCCAGGCCCATCGGTGACGGCTCCACCGCCGACACCGGCCCGCAGCCCCACCAGCCCGACCGGCCCGTGCCGCTCCAGCCGGGCGAGACGCCGCCGCAGTTCGTGGTCTTCAGCTGGGACGGCGCGGGGGAGATCGGCAACGGCCTCTTCCCGCGCTTCCTCAAGCTCGCCAAGGACCACGGCGCGGCCATGACCTTCTTCCTCTCCGGCATCTATCTGCTGCCCGAGTCGAAGCGGAGCCTCTACCAGCCGCCGAACAATCCCGTCGGCGCGTCCGACATCGGCTACCTCAAGGACGAGAACGTCCGCACCACCCTCCGCCTCGTCCGCGAGGCGTGGCTCGACGGGCACGAGATAGGCACGCACTTCAACGGCCACTTCTGCGGGGGCTCCGGCTCCGTCGCGCGCTGGACCCCGGCCGACTGGGAGAGCGAGATCGACCAGGCCGTGTCCTTCGTCACAAACTGGCGCACGCACACCGGCTTCACCGATGTGGAACCGCTGCCCTTCGACTACCGCAAGGAACTGACCGGCGCCCGCACCCCCTGCCTCCTGGGCCGGGACAACCTCCTGCCGACCGCCCGGAAGCTGGGCTGGCGCTACGACTCCAGCTCGCCCGGCGGCCTCCAGGTCTGGCCCGTGCGCAGGTCGGGCGTCTGGGACCTGCCGTTGCAGTCCCTGCCCTTCCCGGGCCACTCCTTCGAGGTGCTCTCGATGGACTACAACATCCTCGCCAACCAGTCGAAGAACACCACGAAGGGCGTCCCCGCCCACTACCCGGCCTGGCGGGCCCAGGCCACGGCCACCTACCTCGGCGGGTTCCGCCGCGCCTACGAGACCAACCGCGCGCCGCTCTTCATCGGCAACCACTTCGAGGAGTGGAACGGAGGCATCTACATGGATGCCGTCGAGGAAGCCCTCAAGGGCATGGCGGACAAAAGGGATGTAAGGCTCGTGTCCTTCCGGCAGTTCACCGACTGGCTGGAGGCCCAGGACCCCAAGGTTCTCGCCCGGCTGCGCACCCTCGGCCCCGGCCAGTCGCCCGCCGGCGGCTGGAACGCGTACCTCACCGCGGCCTGAACCATCGCCTGACCAGGGCATTGACACCCGGCCGGGGGGCGCGGAAAATCCGCGAATTGCTCATGCGAAACTTTTCACATGAGCCTTAGCCGCGCCCCCCGACGCCGCTCACCCAGCGGCCGCGCCCTCCTGCTGACCGCGGTGACCGTCACCGGCGCCCTCACGCTCACGGCGTGCGGCGGCTCGGACAGCGGCAAGCCGACCGGCAGCGGCGGCAACTACGTCACGGGTGCGAGCGGCATCTCCACCGCCGCCGAGGGCGAGCGCGTCGAGGCCCCGGGGCTCGACGGCGAGACCGTCGACGGCAAGCCCCTCGACACGGCCGCCCTCAAGGGCAAGGTCGTCGTCCTCAACGTCTGGGGCTCCTGGTGCCCGCCGTGCCGCGCCGAGGCCCCGTCCTTCGCGAAGGTCTCCAAGGAGCTCGCCGACGCCGGCAAGGACGTCGTCTTCGTGGGCGTCAACGTCCGCGACAACAGCAAGCAGAACGCCGCCTCCTTCGAGGAGACCTTCGGGATCACCTACCCGAGCCTCTACGACCCCGACGGCAAGCAGCTGCTCCGCTTCCCCAAGGGCAGCCTCAGCCCGAACGCCATTCCCTCCACCCTCGTCCTGGACCGCGAGGGCCGGATCGCCGCACGCACCCTCGCCCCCCTCAGCGAGGAGCAACTGCGCTCGATGATCGACCCCGTCCTCGCGGAGCAGTGACCTCGTGGTCGAGTACGTCCTCGCCGCCGAGGCCACGGGTGTGAACGAGACGGTCCTGAACGGCGCCCTGCTGCTGGCGGTGCCCATCGCACTCCTCGCGGGACTCGTCTCCTTCTTCTCGCCCTGCGTCCTGCCGCTGGTCCCCGGCTACCTCTCCTACGTGACCGGCGTCAGCGGCGCCGACCTCGCCGAGGCCCGCCGAGGGCGGATGCTGGCGGGCGCCGCCCTGTTCGTCGCCGGGTTCACCGCCGTCTTCGTCTCCACCGGCGCGCTCTTCGGGTACTTCGGCTCCGAGCTCCAGGAGAACAAGGCGATCATCTCCCGGGTGCTGGGCGCCCTGGTGATCGTCCTCGGCCTCTTCTTCATGGGAGCCATCCCCGGCCTGACCATGCGGGAGTTCCGCTTCCACAAGAAGCCGACCGCCGGCCTGCTCGGCGCGCCGCTGCTCGGCGTGCTCTTCGGCGTCGGCTGGACCCCCTGCATGGGCCCGACCCTCGCCGCCGTCAACACCCTCTCCATCGACCAGGCGAGCGCCGGCCGCGGCGCCCTGCTCACCGTCGTCTACTGTCTGGGCCTCGGCGTGCCCTTCATCCTCGCCGCGATCGCCTTCCGCAAGGCGCTCGGTGCGTTCGGCTGGGTGAAGCAGCACTATGCATGGGTGATGCGGATCGGCGGCGGCATGCTGATCCTCACCGGCCTGCTGCTCGTCACAGGTTTGTGGGACAGCATCGTCACCGACATGCAGGCCTGGACCCAAAGCTTCACGGTGGGGATCTGAGGAACCGACGGACATGAGTACGACAGACAAAGCGTCCACCGAGACGTCGCCCGAGCCCTCCCCGGCGGACCCCTCCGAGGCCGCGGCCGGCTCCCAGCTCTCCACCGCCCCCGTCGAGGACAGCGGTCCCGTCGGCATCGGCGTGATCGGCTGGGTCCGCTGGTTCTGGCGGCAGCTCACCTCCATGCGGGTGGCGCTGATCCTGCTCTTCCTGCTGTCCCTGGGCGCCATCCCCGGCTCCCTCGTCCCGCAGACCGACGTGGACGCGCTGAAGGTCGCCCAGTGGAAGAAGGACAACCCCTCCTTCGTCGGCGTCGCCGAGGCGTTCCAGCTCTTCGACGTCTACAGCTCGGTGTGGTTCTCCGCGATCTACCTGCTGCTGTTCGTCTCGCTGATCGGCTGCATCGTCCCGCGCGCCTGGCAGTTCGTCGGCCAGCTCCGCGGCCGCCCGCCGGGCGCCCCCAAGCGGCTCGACCGGCTGCCCGCCCACACCACGTGGCGCACCGACAAGACCCCCGACGAGGTCCTCTCGTACGCCAGGACGCTGCTCGCGGGCAAGCGCTTCCGCACCGAGGACGGCAGCGGCACCGTCGCGGCCGAGAAGGGCTACCTCCGCGAGGCCGGGAACCTGCTCTTCCACGTCGCGCTGATCGTGATGCTCGTGGCCTTCGCCTGGGGCCAGTACTTCAAGTCCGAGGGCGGCAAGCTGGTCCTGCGCGGCAGCGGCTTCTCGAACACGCTCACCCAGTACGACGACTTCAAGCCCGGCACGCTCTTCCACCCGGACGACCTGCCGCCGTTCAGCTTCACCCTGGACCGCTTCGACGCCACCTACGAGATGTCCGGCCCGCAGCGGGGCACCCCGCGCGACTTCAAGGCGCACGTCACCCTCACCGAGGGAGCCCACGGAAAGCCCGAGAAGCGCGAGATCCAGGTCAACGAGCCCTTGGAGATCGACGGCTCCAAGGTCTACCTCCTCGGCCACGGCTACGCGCCGATCATCTCCGTGACCGACTCCACCGGAAAGGTCGTCTACAAGGACGCCGTCCCGGTGCTCCCGCAGGACGGCAACCTCACCTCCACCGGAGCGGTCAAGGTCACCGACGGCTACAAGGACAAGGACGGCAAGGCGGAGCAGCTCGGCTTCACCGCCGTCTTCGTGCCGACCTTCGCAGGCGAGGGCAAGGGGACGATGTTCTCCCAGTTCCCCGCCCTCCTGAACCCGCAGCTCATGCTCAACGCCTGGCACGGCAGCCTCGGTGTGGACTCGGGCCTGCCGCAGAACGTCTACCGCCTGGAAACCTCCAAGATGGAGATGTTCAAGGACGAGTCGGGCCAGCAGCTCATCAAGAGGCTGGCGCCCGGCGAGACGATGGACCTGCCGAACGGCGCGGGCACCGTGAAGTTCGAGGGCATCGAGCGCTGGGCCACCTTCTCCGTCACCCAGCAGCCCGGCAGCGGCCTCGCCCTCGCGGGCGCGATCGCCGCCATCGCGGGCCTGGCCGGTTCGCTGTTCATCCAGCGCCGCCGGATCTGGGTGCGCGCGGTGGAGGGCAAGGACGGCGTGACCGTCGTCGAGATGGCGGGCCTCGGCCGCAGCGAGTCCGCCAAGCTTCCGGAGGAGCTGGCGGACCTCGCCGCCATGCTGCACCAGCAGGCGCCCAGCGTGTCTGATCCTGTTGAAGAAACCCCTGAAGGAGAGCGCGGATGACGCCGCTCGCAGCCGCAGCCAACGAGAACCTGGCTGAGATCAGCAACTACCTGGTCTATTCGTCGATGGCGGTCTACACGCTCGCCTTCTTCGCGCACATCGCCGAGTGGACCTTCGGCAGCCGCAGCAAGGTGGCCCGCACGGCCGCCGCGCTGACCGGCACCGCCGGTGCCGCGGCACCGGCCGTGCAGGTGCGCGGCAAGGGCGGCGCCACCGCCGTACTGGACCGGCCCAAGGTCACCACCCGCTCCGGCGCGGGCACCCGCGACGTCCCGGACGGCCCCGGCGCCGCCGGCGGCACCGTGCAGGGAGACCTGTACGGGCGGATCGCGGTCTCGCTGACCGCGCTCGCCTTCCTCGTCGAGGCGGCCGGCGTGGTCACCCGCGCCCTGTCCGTCGAGCGGGCCCCCTGGGGCAACATGTACGAGTTCTCGATCACCTTCTCCACGGTGGCCGTCGGCACCTACCTGGTGCTCCTCGCCCTGAAGAAGAACGTCCGCTGGCTCGGCCTGATCCTGGTCACCACCGTCCTGCTCGACCTCGGCATTGCCGTCACCTGGCTCTACACCGACAGCGACCAGCTGGTCCCGGCCCTGCACTCCTACTGGCTGTGGATCCACGTCTCCACCGCCATCTTCTGCGGCGCCGTCTTCTACCTCGGCGCGGCCGGCGCGGTCCTGTACCTCTTCCGCGACTCCTACGAGGCCAAGCTCGCCGGCGGCGGCAAGCCCGGCAGGATCGCCTCGTCCGTCCTGGAGCGCCTGCCCTCGGCGGCCTCGCTCGACAAGTTCTCGTACCGCATCAACGCGGCCGTCTTCCCGCTGTGGACGTTCACGATCATCGCGGGCGCGATCTGGGCGGGCGACGCCTGGGGCCGCTACTGGGGCTGGGACCCCAAGGAGGTCTGGTCCTTCGTGACCTGGGTGGCGTACGCCTGCTACCTGCACGCCCGCGCCACCGCCGGCTGGAAGGGCCGCAAGGCCGCCTACCTGGCGCTCTTCGCCTTCGCCTGCTGGATCTGGAACTACTACGGCGTGAACATCCTGCTCAGCGGCAAGCACTCGTACGCGGGCGTCTGACCGGCCGGAGTGGGACGCTGGTGGCATGTCCCTCGTGAGCCATGCCACCAGCGAACGGCGCGGCGAGAACCACTGGCTGCTCCGCTTCGAGCTGCACCTCCCCTACGCCTACGAGGCCCTCTGGCACGCCCTGACCACACCGGACGGGCTGCGCGGCTGGCTGGCCGCGGCCGACGTCCTGGAACGGCACCTCGGCGGGGCCGTGACGCTGCGCTGGCTGAACACCGCAACCGTGGCGACGGGCCACGTCACGGCCTGGGACGTGGAACGCGTCGCCGAGTACACCCTGAGCGGGCAGGGGCGGATCCGCTTCCACCTGGAGGCGGTCGGCACCGATTCGACGGTCCTGCGGTTCCTGAACGAGCGCGGCGGCACCGAGGAGGACCGCCTCGACTGCCTGGCCGGCTGGCACGAGCACTTCGAGCTGCTGGAAGCCGCCCTGGCCGGCCGCCCGGCGGACTGGTCCTCCTGGACGGACACCCGCCGGGCGCGGCTGCGCGAGTCGTACGGATCCTTCGGCAGCGCCCGCAAGGCCTCCTGAGCCCCCACCCGGCCGCCCCGCGCCCCCCGCACAGGATCACCACACCGGGCGCAGGGGTGGCAGCCCGTCCTGCCCGTGCAGCGCGCGCACGACGCGGGCCAGCTCCCGGCGCAGGGCGCCGATGTCCGCGCTGCCGGCGAGCTCCGCCTCCAGCTCGTGCAGGATCCGGCCCGCGACGGCGAGGTGTTCGCGCGCCGCACCCGTCAGGACGACCAGCTTGCGGCGCCCGCCCTCCGGGTGCGGCTCGCGGCGGACGTAGCCGCGCCTCTCCAGGTCGTCGACGATCTGCCCGGCGGCCTGTTTGGTCACCCCGAGCCGCTCGGCGAGCTCGGTGGCGGTCGCGCCACGCCCCTTCAGGGCCTGGAAGGCCATGCCGTGCACGGGCCGCAGGTCGGCGTATCCGACCTCGGCGAGGCGCCGGGTGAACTCGCCCAGCACCAGTTGGAAGCCCAGGCCGAGCAGGAACGTCAGCTCGACGCCCCCGCCGCTCTCCATCGCGTCTTCTCTCGTCACGCAAACATGGTGACACGGGTGGGTCAAGCTGCTTTACTCGCACAAGTAAAGCGGCTTGACTCATTCGTCGAGGAGGACTCGCCTTGTACGTGATCACCACTTCCCCCGACCACGTCACCACCACCCCGAACGCCGCCATGACCGGCCTCGCCGCCCCCAGCCGCGGCAGCTCGGAGCTCAGCACCTGGCAGGTCGACATGCCCGCCGGAGCCACCGGCCCCGAACACTCCGTCAGCCGCGAGCAGGTCTGGACCCTCACCGCCGGCTCCCTGGAGGTCACCTCCGACGGCCGCACCCAGAAGGTCACCACGGGCCAGACCCTGGTCCTCCCGGCGGACGCGCCGCGCAGGATCCACGCCGCCGAGACCTTCCGGGCCCATGTGGCGATGCGCGCGGACGGCGTGGTGTCGGTGCCGGGCGAGGAGGAGCCCCGCGTCCTCCCCTGGGCGCGGTAGCCGGGCCCACGACAGGACGGGCCGGCCGCCCGGGCCGGCCGCCCGGGCCGGCTAGTCGGCGTCCTTGCCCTGGTCCTTGCCCTGGTCCTTGCCGTTGTCGCGGTCGCGGTCCTTGTTCTCCTGCTCCTCGCGCAGGGACTTCAGGAACTCCGGATTGTCGTCGGGAGCCACCCACCGGCTGCGGCCCCGGGGCCCGCGCCCGCCGCCGCCGGAGACCACCCGCTTCTTGCCCGCGAACAGCCACACCACCGGCCCCACGATGGAGAAGAGCAGGATGATGATCACCCACATCGCCTTGGGGAGGTGCTTGACCTCTTCCTCGGGCGTGTTCAGGCAGTCGATGAAGGCGTAGATGGTCAGCGCGATGATCAGCAGGAACGGCAGATAGCGCAACACGGTGTGGGACCGACTCCCGGGCAGTGGCGGCGGACCCGCGAGGGGCCCCGGTGACGCTCCCAGCGTAGTTGGTGACGGATACTGACCCCTATGGCTTACGACGATCTCCGCTCGCTGCTCCGGGCTCTGGAGCGAGAGGGCGACCTCAAGCGCATCAAGGCCGAAGTCGACCCGTACCTGGAGGTCGGGGAGATCGTCGACAGAGTGAACAAGGCGGGCGGTCCCGCGCTGCTCTTCGAGAACGTCAAGGGCTCGGCGATGCCGCTGGCCATGAACGTCTTCGGCACCGACCGCCGCCTCCTGAAGGCCCTCGGCCTGAAGTCGTACGCCGAGATCAGCGAGAAGATCGGCGGCCTGCTGAAGCCGGAGCTGCCGCAGGGCTTCATCGGCGTCCGCGAGGCCTTCGGCAAGCTCGGCTCGATGGTCCACGTCCCGCCGAAGAAGGTGAAGGGCGACTCCGCGCCCGTCCAGGAGGTCGTCCTCACCGGCGACGACGTCGACCTGGACCTGCTGCCGGCCCTGTTCACCTGGCCCAAGGACGGCGGCTCCTTCTTCAACCTCGGCCTCACCCACACCAAGCACCCCGAGACGGGCGTGCGCAACCTCGGCCTCTACCGCCTCCAGCGCCACGACAAGCGCACCATCGGCATGCACTGGCAGATCCACAAGGACAGCCGCAACCACTACGCCGTCGCCGCCGCCAAGGGCGAGCGGCTGCCGGTCGCGATCGCCTTCGGCTGCCCGCCCGCGGTCACGTACGCCTCCACCGCCCCCCTGCCGGGCGACATCGACGAGTACCTCTTCGCCGGCTTCGTCGCGGGCAAGCGGATCGAGATGGTCGACTGCAAGACCGTCCCGCTCCAGGTCCCGGCCAACGCGGAGGTCGTCGTCGAGGGCTGGCTGGAGCCCGGGGAGATGCTCCCGGAGGGCCCCTTCGGCGACCACACCGGCTTCTACACCCCGCAGGAGCCCTTCCCAGCCCTGAAGATCGACTGCATCACGATGCGCAAGCGGCCGCTGCTGCAGTCGATCGTGGTGGGCCGCCCGCCGACCGAGGACGGCCCGCTGGGCCGCGCGACGGAGCGGTTCTTCCTGCCCCTGCTGAAGATCATCGTCCCGGACATCGTGGACTACCACCTCCCCGAGTCGGGCGGCTTCCACAACTGCGCGATCGTCTCGATCGACAAGAAGTACCCCAAGCACGCGCAGAAGGTCATGCACGCCATCTGGGGCGCCCACATGATGTCGCTGACCAAGCTGATCATCGTGGTGGACAAGGACTGCGACGTCCACGACCTGCACGAGGTGTCCTGGCGGGCCCTCGGCAACACGGACTACTCCCGCGACCTCACCGTCGTCGAGGGCCCGGTGGACCACCTCGACCACGCCTCCTACCAGCAGTTCTGGGGCGGCAAGGCGGGCATCGACGCGACGAAGAAGCTGCCCGAGGAGGGCTACACCCGCGACGGCGGCTGGCCCGACATGGTGGAGTCCGACCCCGCGACGGCCGCCCTCGTGGACCGCCGCTGGAAGGAGTACGGCCTGTGAGCCCGATCGCCGTGAGCGGCCCGGAGCTGAACCTCGGCACCGAGGAGGCGTACGTGGTCCTGGCGCGCCCGAAGATCGACCCGACCCAGCCCGGCGTGATCGCCGCCGCCCGGGAGGCGGGTGTGAGCCCGGAGGAGTTCGCCGGTCCCGGGGACGTCTGGACGCTGATGTACGACGCGGACGGCGACGGCGACGGCTTCGAACTGCCCGGCGCGCGGGACACCGAGGCCGACGCCTTCGCGGAGCAGGTGCAGCAGGCGCTGGCCGCGGCCGAGCCGTTCACCGTCGAGGCCGGAAACTTCCTGCGCCTGGACGCCCGTCCGGCCGGCGCCGACTGGGTGGTCACCGCGCACGTCACCCCGCCGGAGGGCGAGGAGGACGGCGCCGCGGCCCGGACGCTGGAACTCGGCGCGCTCCCGGCGGCGGACCTGCTGGCCGAACTCGAACAGTTCCGGAGGGGACTCGCATGATGACGACCGCCGACGGAGTGGTCGGACAGGGCCCCGCGCCGGAGGCGGCCAACAAGGTCAGGGCCTTCCTGCGGCTGGTGATGATCGAGCACTCGGTCTTCGCGCTGCCGTTCGCCTACATCGCGGCGCTGACCGCGATGTTCCAGCTCGACCGGACCGTGCACTGGGGCAAGCTGCTTCTCGTCACCGTCTGCATGGTGGGGCTGCGCACCTTCGCCATGGCCGCGAACCGGATCATCGACCGCGAGATCGACGCCCGCAACCCGCGGACCGCGGGGCGCGAACTGGTCACCGGCGCGGTGTCGGTCCGCTCGGCCTGGACCGGCGCCGCGATCGCACTCGTCGTCTTCCTCGGCTCGGCGGCCCTGCTGAACCCGCTGTGCCTGGCGCTGGCCCCGGTCGCCGTCGTCCCGATGGTGGTCTACCCGTACGGCAAGCGGTTCACGAACTTCCCGCACGCCATCCTCGGGCTCGCCCAGGCGATGGGCCCCGTCGGGGCCTGGCTGGCGATCACCGGCGAGTGGTCCTGGGACGCGGTGATCCTCGGCCTCGCGGTCGGCGTGTGGATCGGCGGCTTCGACCTGATCTTCGCCTGCCAGGACGTGGCCGCCGACCGGGCCGAGGGCGTGAAGTCCGTCCCGGCCCGCTTCGGCGTCCCGGCCGCCCTCTGGGGGGCGCGCGGCTCTCACGTCGTGACCACGGCCCTGCTGGCCTGGTACGCGCTGGCCACGGACGCGGGCCCGCTGTTCTGGGCCGGCCTGGCGATCGTCGTCGTCGCTTTCGTCTACGAGCACACCATCGTGACCCCGCACGACCTGTCCCGCCTGAACCGGGCCTTCTTCACGGTCAACGGCTTCATCGGCATCGCCCTCTTCGTGTGCGCGCTGGCCGATCTGGTGGCCCGCGGACTGAGCCTGTAGCTCGCAGGAGTGAGCCGGGCAGGACCGCGGGGTGCGCGGTCTGCCGGGTGCGTAGCGTGCGGCCTACCATCGAGTGCATGGACAGGGAGGCCGACGTGACCGTCTCGGAGAGCGACAGCCTGCACTCACAGCTCAGCCGGTTCGAGGACATGTTCCCCGGATACCGGACCGAGATTGTCGAGGGTGCCATCGTGATGAGCCCGGTCAAGCCCCACCACAATGAGACGATCTGGGACGTGCGGGACTTGTTGAAACCGCAGCTTCCGCCCGGGTGGGCCTTCATCTCCGATGTCGCGGTCCCCTTCGACGAAAGCAACGAGTTCTGCCCGGACCTCGCCGTCATTCCGGATGCCGAGCGCCGCAAGAACCTCAGCGCCTATTCCCCCGACCTCATCGAACTGGCCGTCGAGGTCGTCTCACCGAGCAGCATCCGCAACGACTACGAGGTCAAGGACCGGGCCTACGCCCGGCGCGGGATCCCGCACTACCTGATCTTCGACCCGTACAAGGCGCACTGCGTGACCCTGTGGAACCCCGGCCCGGACGGCTACCGGGGCCGGGACACCATCCCGTACGGCGGCGAGGTCACCGTCGAGACCGGCATCGGCAAGCTCGTGATCGACACCTCGGGCCTGCCCGTGGACCCTTCCGTCGTCAGGCCGTGACGGCCGGGCGGCGGGCCGGGCGGCGGAAGTAGAGCGCCGTGACGATGCCGGCCACCAGACCGCACAGGTGGCCCTGCCAGCTGACGCCCGAGTCCGTCGGGAGGATGCCGGAGACGATCGTGGTGCCCCAGACGGCGGCGACGCCCACGGCCACCGCGATGCCCAGCGCCCTGCGCTCGACGAAGCCCCGCACGAGCAGGTAGCCGAAAAGGCCGAAGACGATGCCGGACGCACCCAGCGTCATGGTCCCGGACGGGGATATCAGCCAGGTGCCGAGGCCGTCGGCCAGCAGGATCAGGCCGCACACCGCGAGGAACCGGCGGATCCCGGACAGGGCGGCTATGAAGCCGAGGACCAGCAGCGGGACGCTGTTGGAGGCGACGTGGTCGAAGCCGAAGTGGAGGAAGGCGGCGGAGACGATGCCGCCGAGGCTGTCGGGGTCGCGGGCGACGATCCCGTACTGGTCGAGGGCGTGGCCGGTGGCGTGGTCGACGGCCTCCAGCAGCCACAGCAGGGCCACCCAGCCCAGCATCAGCTTCGCCGCCGCCTTGGCGCGGTCGGTCTGCGTCCAGCCGGTATCCACCGTCGTGCTCAT

Protein sequences of DBSCAN-SWA_2

>NZ_CP019798|4647861:4705525|4657554_4657980_+|WP_078094864.1|DBSCAN-SWA
MGLPLLVARVPTSKEVVFLAFDGGWNHDPAAARILLDRRVPVSLFSLPGAASYDAGYFTGLTQEGRAGVENDTVTHPDLTTLDAAGRVADAGRGSSSGLSSGGCRSLCGRRTGGELRGAARGQGVRGEGAGHLDTRLDHLG
>NZ_CP019798|4647861:4705525|4679262_4679760_-|WP_078094870.1|DBSCAN-SWA
MRRRTVTAGSLEEILQVTAPAQAPEQAAAAPAAAAPRPREDHGLRTEYEFELPRGYVDEAGTVHRHGSMRLATARDELRPQIDLRVKENPAYLSVVLLSQVITRLGTITDVHAGVVERMYATDVAFLQDFYRRVNSEGHTRAAVTCPHCDGGFEVDLSGGRLGES
>NZ_CP019798|4647861:4705525|4661276_4662173_+|WP_060180869.1|DBSCAN-SWA
MLAAVVTGFGGPERVELAEVPVPRPEAGQVRIRVAAAGLNPVDAGVRAGIFGGAGQRLGLGWDVAGEIDETGPEVTGWSRGDRVVGLHYGPVKPLGTHAEYAVLDAAAVAAAPAAVDDLAAAALPLAGLTAARAVEQLGLAPGSSVLVTGAAGVVGGLAVQLAARAGLVVTALAGPGDEELVRSLGAAAFVPRGGAPAGPVDGVLDAAVLGGAALARVRDGGVYVGLIPNHAPAAERGIRVEEQEVAADGELLARLVSLVDEGALTLRVGDVFPLAEAAKAHERLAAPGVRGRIILTA
>NZ_CP019798|4647861:4705525|4672184_4672607_-|WP_030851958.1|DBSCAN-SWA
MSERFIGRGWAFPLRVGPTGGIAMVDRERELEEAIRLVLGTAPGERPMRPEFGCGIHEYVFAPGDGDTAGRVAQQVREALERWEPRITVDDVVVAFDSVEAGTLYIDVHYTVRTTNDRRNLVFPFYTIPSEEGAEEMVAD
>NZ_CP019798|4647861:4705525|4665465_4666320_+|WP_078094866.1|DBSCAN-SWA
MRGSPRSPRSTRTSAPARRSSSYAAERRRTAPKGAPMTDPAGSPAAGRAVDPAAGPAGGPALDPAPVIEMAGIAKTYPGPPPVHALTDVTLDIRPGRLAAIVGPSGSGKSTLLSVLGLLDVPTRGRYLLQGRDTTALSERARTALRASTLGFVFQAFHLVPHLTCVQNVALPLVHLGVPRALRRPQAVAALESVGLGHRLDVRPTTLSGGERQRVAVARAIVHRPAVVLCDEPTGNLDTANSARVMDLLTGLVAQDRAVVVVTHEPEVAARADRVFKVVDGRVS
>NZ_CP019798|4647861:4705525|4699999_4700458_-|WP_060181043.1|DBSCAN-SWA
MESGGGVELTFLLGLGFQLVLGEFTRRLAEVGYADLRPVHGMAFQALKGRGATATELAERLGVTKQAAGQIVDDLERRGYVRREPHPEGGRRKLVVLTGAAREHLAVAGRILHELEAELAGSADIGALRRELARVVRALHGQDGLPPLRPVW
>NZ_CP019798|4647861:4705525|4651659_4653030_-|WP_078094861.1|DBSCAN-SWA
MAAMQLTRTHRILIGVVVAGAVVIAGIGFAGSYSAVRELAEKKGFGSFSLVFPIGIDAGICVLLALDLLLTWMRIPFPLLRQTAWLLTAATIAFNGAASWPDPLGVGMHAVIPILFVVTVEAARHAVGRIADITADRHMEGVRITRWLLSPVPTFKLWRRMKLWELRSYEQAIGMEQDRLIYQARLQARYGRFWRQKAPVEALMPLKLARIGVPLSQTTPDALAATGIDPAVLPPLEQQVAGTAPALEAPATGAVAGAAAGAPEWDDPARQSQQSQQADQAQPQQLSAQVQQVAPAPATPHAPPAFAVDPTAMPAAHNSAWFAAPKAPQAAYEGGYNPQYVEGLEPTPVLPPMGPDDQQAQQLPVPEPRHEGAPDGDFPEQVPEVDSPDEVEFAQIAYKVFCSLAEETQDYPTAEALDIVLADRYGVTHPRSGSLLRRMISSFRQQHHKDREAEPA
>NZ_CP019798|4647861:4705525|4654032_4654893_-|WP_107052362.1|DBSCAN-SWA
MLTALAAGAAGLTGCTGGSDGGSTSDSKAGGSSAAPAQPGKYRSLPAPCRAAADSKKLKAMLPAPDSLTPQQRDQLYAGVADASYDGDRHVGCRWTAQTPEETRLLSVGFERVVSYDRGAASDDDKAKQVYVRLLTDAHLPFPGPVTTPGPGAANPGNPANPANPAASTPPPAAPPAAPPASGAPSAGAPAAGTPAPGTSPSAQPELGSRVLEGLGTEAFLDDKLSAAGATAAQSRTVRIVFRTSNVIVKIEYSVQPTLPGTIPPSGETQDKARQLAQALAERLNE
>NZ_CP019798|4647861:4705525|4647861_4649631_-|WP_078094859.1|tRNA|DBSCAN-SWA
MASVPSLASSVNQRVADALASALPEAGGADPLLRRSDRADFQANGILALAKKAKANPRELATTVVGGIPTGDLIKEIEVSGPGFLNITVADGAIISTLAARAADDRLGVPLNASAGTTVIDYAQPNVAKEMHVGHLRSAVIGAAMVEILEFTGEKVIRRHHIGDWGTQFGMLIQYLLEHPHELDHRSGDGDEQASGEEAMSNLNRLYKASRALFDSDEEFKTRARARVVDLQAGEPETLALWQRFVDESKIYFYSVFHKLDMDIRDPDVVGESGYNDMLVETCKLLEESGVAVRSNGALCVFFEDVKGPDGNPTPLIVQKSDGGFGYAATDLSAIRDRVGNLGATELIYVVDARQSLHFKMVFETARRAGWLNDDVKAVQLAFGTVLGKDGKPFKTREGETVRLVDLLDEAIDRASAVVREKAQDLTEAEIAERGAQVGIGAVKYADLSTSAARDYKFDLDQMVSLNGDTSVYLQYAYARIQSILRKAGDAKPAAHPEVALAPTERALGLHLDGFGELIAEAAAEHAPHKLAAYLYQLASLYTSFYSECPVLKADTAEQVENRLFLCELTARTLSKGMSLLGIRTPEKL
>NZ_CP019798|4647861:4705525|4691007_4691616_-|WP_076043866.1|DBSCAN-SWA
MQRGGGPGEGTDGLDPQRAREAREARRRGKHRRRATEAADAVPEPAAEPEDVPRGRGMGVTYKYFGAPDGATAARVPVTMRPEELGGDELGMGGLFTKIKPETVAAMVLTGIEGIPLHKVPPLELVVLHPDYAVVKLPMTVVDPLRGIGEESVGAAAFIWSTVPDRGGPSDAFNVYQLLHEWQDFSHRLHEAGHQPYCLVWP
>NZ_CP019798|4647861:4705525|4656396_4657215_-|WP_078094863.1|DBSCAN-SWA
MADQDPSAPGRFMDLQDPRYAYMFGFLQADGHLAQGSGQKGKLTAEVNARDIEILREFQRLTPYYSSISERTRATNFSESHTSATWSLCSLEARSAINELGLPYGPKSMNIRPPRVDFSRRDYLRGVIDADGSVGYTNTGLPFVSLTTASTALGAYLCHYAKKITGAERTIKRNTRDGIYNILYTKEAAQALAAHLYYEGCLGLGRKKARAAELLNWVRPADMRVAPPRRRWTPKDDETLLRLNDPAAAGIALDRTAQSCSMRLWRLRTGKA
>NZ_CP019798|4647861:4705525|4658954_4659290_-|WP_060180868.1|DBSCAN-SWA
MLIARSAALFSLAALLEIGGAWLVWQGVREHRGWAWIGAGVIALGLYGFVATLQPQGDFARVLAAYGGVFVAGSLAWGALADGYRPDRWDVVGALVCLAGMAVIMYAPRGR
>NZ_CP019798|4647861:4705525|4689388_4690672_+|WP_060181048.1|DBSCAN-SWA
MPGGTATTSLTVRNDSDIVEAYRLEVVGDCAAWTTVEPARVSLYPGTSETVTIRLAPPRSPQVRAGDVPLAVRVLPTEQPDAVRVPETTVHVEQFRELRAESAPKRRRGWLRGRYRIAVRNEGNAPVKVGFTPAQPGEELKFDFAPPTLKLEPGESAEVVLKVRAAGPVWFGAPVTWPFTVEVAETAEGGDGEDAAARAEHEAVRGPLEVEFVQIPIFPTWLLAVLAALLALLLAWFMLVRPAVRSTAKEAAAEAARNPAPAADAAGQTPVTGGGKQPGGAGAGPGAAKGNQPGAGGGGSGTGAGGGGGGLQSSATIDLQTGGGQSKTGSYTVPAGKVFGITDIVVANFQGDEGVVTINFGDRKITTIALETFRNQDYHWVTPISITESQTVTVQVTCAKPGTPATGRQAQECHEVLNVSGVLSDLR
>NZ_CP019798|4647861:4705525|4679756_4680197_-|WP_030031999.1|tail|DBSCAN-SWA
MAEGDALSTHIFGVQLGGYLVESIQEISGLTVEEEVVEVRQVSAEGKQIIRKQPGARQAGEVTITRGLDKSSEFTKWIKETLNNGAVDTARQNLTIEIKDSTGATIRRIQLMQGWASKWEGPSLKAGESAAATESVTIVFEEIIVE
>NZ_CP019798|4647861:4705525|4649810_4651550_+|WP_078094860.1|tRNA|DBSCAN-SWA
MAQSAQSSTETDWVSRFADEVIAEAERRAPGKAVVVASGLSPSGPVHLGNLREVMTPHLVADEIRRRGHEVRHLISWDDYDRFRKVPKGIPGVTEESHAQHIGRPLTAVPAPEGSAYPNWAEHFKAAMAESLAELGVEYDPISQTEQYTTGVYREQILHAMKHRGDIDAVLAQYRTKVKPGGKKPQQKQVDEAELEAAEGSGAAAEDDGSAGEGGYFPYKPYCGRCGKDFTKVTSYDDETTEMTYVCTEDDFTETVKLSEFNRGKLVWKVDWPMRWAFEGVIFEPSGVDHSSPGSSFQVGGQIVHIFGGEQPIGPMYAFVGISGMAKMSSSKGGVFTPGDALQIMEPQLLRWLYARRRPNQSFKIAFDQEIQRLYDEWDKLEGKVADGSVLPADAAAHARAVRVASHELPRTPRPMPYRTLASVVDITAGHDEQTLRILSDLEPDKPLTSLDEVRPRLDRAENWITTQVPADQRTLVREDADTELLSSLDDEGRESLRLLLDGLDSHWSLDGLTTLVYGVPKVMAGLEPDAKPTPELKVAQRTFFALLYRLLVTRETGPRLPTLLLAVGADRVRKLLAV
>NZ_CP019798|4647861:4705525|4666309_4667590_+|WP_143568901.1|DBSCAN-SWA
MFRSRRTRERSADVEAGSDAEGTAPAAPRTSAADLLVQAFLALFGRRFRTLLTMVGISVGLAAALATLGITASAAGAVSDQFDALKATRVTVKYPSEPVAGVRPRPDGGDTQRVRGLNGVRTAGLVSKAGEQPVVSRLASGGSNDLPEGTVLAAQPDALPAMSAELTQGRWFDTGHDARRERVALIDTAAASRLTVDGGAGNSVIHVNGVAFSVLGVFRAPTGDTDLTGSVVVPYWAALQDPAGLGFAPAEMIIRTDLGAADQIGAEAPFALAPGAPDKLVALVPPDPRSLRQGVESQTRALFLGLAAVSLGVGALGVSNTAYVSVLERRSEIGLRRALGASRRAVAGQFCIESGLVGLAGGVVGTVLGIQITAVTCLAKNWLVVLDPVLTTAGPLVGLVVGLAAGLYPALAAARILPAETLRAGV
>NZ_CP019798|4647861:4705525|4704342_4704930_+|WP_078094876.1|DBSCAN-SWA
MDREADVTVSESDSLHSQLSRFEDMFPGYRTEIVEGAIVMSPVKPHHNETIWDVRDLLKPQLPPGWAFISDVAVPFDESNEFCPDLAVIPDAERRKNLSAYSPDLIELAVEVVSPSSIRNDYEVKDRAYARRGIPHYLIFDPYKAHCVTLWNPGPDGYRGRDTIPYGGEVTVETGIGKLVIDTSGLPVDPSVVRP
>NZ_CP019798|4647861:4705525|4672606_4672924_-|WP_030851960.1|DBSCAN-SWA
MPAAARTGDPTNHGGRLATPPPGAAAQVATVLIGGRPAAVVGSLHVCVVPPHAALGPANVIVPNPAALASGTVLIGGLPAARARDQTACGAMVLTGALDVLIGGV
>NZ_CP019798|4647861:4705525|4698339_4699422_+|WP_030855559.1|DBSCAN-SWA
MTPLAAAANENLAEISNYLVYSSMAVYTLAFFAHIAEWTFGSRSKVARTAAALTGTAGAAAPAVQVRGKGGATAVLDRPKVTTRSGAGTRDVPDGPGAAGGTVQGDLYGRIAVSLTALAFLVEAAGVVTRALSVERAPWGNMYEFSITFSTVAVGTYLVLLALKKNVRWLGLILVTTVLLDLGIAVTWLYTDSDQLVPALHSYWLWIHVSTAIFCGAVFYLGAAGAVLYLFRDSYEAKLAGGGKPGRIASSVLERLPSAASLDKFSYRINAAVFPLWTFTIIAGAIWAGDAWGRYWGWDPKEVWSFVTWVAYACYLHARATAGWKGRKAAYLALFAFACWIWNYYGVNILLSGKHSYAGV
>NZ_CP019798|4647861:4705525|4699447_4699963_+|WP_060181044.1|DBSCAN-SWA
MSLVSHATSERRGENHWLLRFELHLPYAYEALWHALTTPDGLRGWLAAADVLERHLGGAVTLRWLNTATVATGHVTAWDVERVAEYTLSGQGRIRFHLEAVGTDSTVLRFLNERGGTEEDRLDCLAGWHEHFELLEAALAGRPADWSSWTDTRRARLRESYGSFGSARKAS
>NZ_CP019798|4647861:4705525|4679107_4679266_-|WP_167344733.1|DBSCAN-SWA
MTYALPRLREEIAYIAYHFHWRRDEILDLTHGERQDWVTEIARINTRVNEGG
>NZ_CP019798|4647861:4705525|4703341_4704265_+|WP_060181040.1|DBSCAN-SWA
MMTTADGVVGQGPAPEAANKVRAFLRLVMIEHSVFALPFAYIAALTAMFQLDRTVHWGKLLLVTVCMVGLRTFAMAANRIIDREIDARNPRTAGRELVTGAVSVRSAWTGAAIALVVFLGSAALLNPLCLALAPVAVVPMVVYPYGKRFTNFPHAILGLAQAMGPVGAWLAITGEWSWDAVILGLAVGVWIGGFDLIFACQDVAADRAEGVKSVPARFGVPAALWGARGSHVVTTALLAWYALATDAGPLFWAGLAIVVVAFVYEHTIVTPHDLSRLNRAFFTVNGFIGIALFVCALADLVARGLSL
>NZ_CP019798|4647861:4705525|4696645_4698343_+|WP_060181045.1|DBSCAN-SWA
MSTTDKASTETSPEPSPADPSEAAAGSQLSTAPVEDSGPVGIGVIGWVRWFWRQLTSMRVALILLFLLSLGAIPGSLVPQTDVDALKVAQWKKDNPSFVGVAEAFQLFDVYSSVWFSAIYLLLFVSLIGCIVPRAWQFVGQLRGRPPGAPKRLDRLPAHTTWRTDKTPDEVLSYARTLLAGKRFRTEDGSGTVAAEKGYLREAGNLLFHVALIVMLVAFAWGQYFKSEGGKLVLRGSGFSNTLTQYDDFKPGTLFHPDDLPPFSFTLDRFDATYEMSGPQRGTPRDFKAHVTLTEGAHGKPEKREIQVNEPLEIDGSKVYLLGHGYAPIISVTDSTGKVVYKDAVPVLPQDGNLTSTGAVKVTDGYKDKDGKAEQLGFTAVFVPTFAGEGKGTMFSQFPALLNPQLMLNAWHGSLGVDSGLPQNVYRLETSKMEMFKDESGQQLIKRLAPGETMDLPNGAGTVKFEGIERWATFSVTQQPGSGLALAGAIAAIAGLAGSLFIQRRRIWVRAVEGKDGVTVVEMAGLGRSESAKLPEELADLAAMLHQQAPSVSDPVEETPEGERG
>NZ_CP019798|4647861:4705525|4653154_4653919_-|WP_051700584.1|DBSCAN-SWA
MHRSASRLTRVLACAAVPVILTVAGCSSDSGKESADKGDKKSGSSASAKPGEKKSKPELEKAAFATLPDPCKAIQAGTIDTLVPEAKDKNGTATKSNDLATRASCSWNGLDEDGLKGSQYRWLSLSYFRTDSHASLGGANKRAEEQYGKQVESAKASEGAQNVKAEAVEGLGDQGTSIVYSVKKDVDFFNTTIVARTQNVVVTLDYNGAAYEGAGAPDQAKLLQDAITAAKEAVASVAGANKPAEQQPQSPQPQ
>NZ_CP019798|4647861:4705525|4684366_4685071_-|WP_078094871.1|DBSCAN-SWA
MIHEVDEGLRRLLAESGLEASGVEVVFDAPTRDWAARRSAPTVCVFLYDIREDPTRRGSGGGEVFDEDGFVVARRTPPRWFELTYLVTAWASRPQDEHRLLSQVLSCLVATDTLPPRLLTGTLADLGLLVDVDAGGTGMDAPAASDVWSALGGELKPSLGLRVKAPLAGISKVTAPPVTQGLVVNSVPQAGPDGDGSPRRLRYVELGTPGPEGFGGSRERPKAPARRRRGERQP
>NZ_CP019798|4647861:4705525|4655125_4656319_+|WP_078094862.1|DBSCAN-SWA
MSYVEVPGAQVPIRMWTDPASVEAGAMQQLHNVATLPWIKGLAVMPDVHYGKGATVGSVIAMKDAVCPAAVGVDIGCGMSAVKTSLTANDLPGDLSKLRSKIEQVIPVGNAMHREAVDPSRLYGFTEAGFGDLWERFDYVADAVKFRRDRAMRQMGSLGQGNHFCEVCIDSSGSVWLMLHSGSRNIGNELAAFHIGVARGLSHNQNLVDRDLAVFLAATPEMEAYRNDLFWAQEYAKYNRAVMMSLFKEVVRKEFRKAKVSFDREISCHHNYVAEERYDGMDLLVTRKGAIRAGSGDYGIIPGSMGTGSYIVKGLGNEKSFNSASHGAGRKMSRTAAKKKFSARDLAEQTRGVECRKDSGVVDEIPGAYKSIEHVIDQQTDLVQVVAKLKQVICIKG
>NZ_CP019798|4647861:4705525|4662645_4663029_+|WP_143568903.1|DBSCAN-SWA
MLSKRISAGFIAMAAVAGVVAAAPSASAVDRTCYDGNFCIYKDRDFSKNNSMYRTKYESARWDIDMPAVYEADSSWWNRRGQSSKTYGGRWMSLGVEICLIPGGSVNYYWDANDDGASNTLNDGSRC
>NZ_CP019798|4647861:4705525|4669448_4669637_-|WP_078094867.1|DBSCAN-SWA
MRACPACGASNAPTDDFCANCGAYLNWSSSTPSPSAAAPAGEAARARPRPDPARDRPGRHTR
>NZ_CP019798|4647861:4705525|4672981_4674799_-|WP_078094868.1|DBSCAN-SWA
MSGSEPGGRSFAADPIVEAPGELPQIWAAQLVSCVVDENVGLPDTAVLTYRDPDHEFLRATGITIGTPLRVSVATVKGQARERLFNGEVTALEIDRDRTGSFTVVRAYSKAHRLQRGRKVVAYRNMTAAAIVRKVAAGAGLAVGKVEAAPVTYKQLSQANVSDWDFLQFLAGESGAQVRVDDKGLLQFTRPVKASGAPAPSTSAVRDPMVLEYGRNLLALRAALSAADGASKVQVRGWDVTTKRPLVAEQPSVVSDTVVPGLGPQTAARFGAASVSVTDTPYRTQAETTAVAKATAAQISSGFGELEAVAEGNPLLRAGKPVALGNVGPAFSGRYTATAVQHVLEPHGGFRTTVWVSASPDRSLTGLVTGANAPGRGPRIPGLAIGVVTDVREPNGSQRGAVRLKFPWLDDTYTTDWVRTVQWGGKGGGGVVSPEVNDEVLVGFEQGLLDSPYVIGGLYNGVDQPSPHDVPLIDRTSGKVNRRSIVSRSGHRVELLDAAAPGPSGLRLVTGDERLEVRMDDRRDRIELTVYAGRGRPLTSVLMDGKGITLDARQGTVKVSGRQVDIDGTAGVSIGGRSVKVSGTSDVTVNGGLLAVLKARLIRIN
>NZ_CP019798|4647861:4705525|4682063_4684172_-|WP_078096289.1|DBSCAN-SWA
MWARLRLVEERVRLAVELRRAADPDPDDPYRGQYLTPEAVARILDEGGEHGPGLPALAPAWPPPPGSPLGVLATRFALEPLDVDLLLVALAPDLDARFERLYGYLNDDLTRRRPTVGLALELCGRARSAAARFRLSPGAPLVAGGLLEVTEPDRPPLSRVLAVPDRVTAHLLGAAAPDPHLAEVLGEAADDPAVDPGELHRAAAAAGNGTGHVHLRTRGGDPEGLAAAALRARGLRPLVLDPAALTHRAHALPALARAAAREARLLGAGVLLGPLEALPDKPDERAHVLRTLCTVLRGIPLFTHGTSGWEPAWAAATPVCLTVAAPSPDRQAVRWRHALERAAAEHGRTDGAAGTGMEGGAGRAEADGAEAGRAEALARSVSAHRLDAGQLRRAADTASRTAALDGRPVSPDDLRSAVRAQNGAGLARLARRVEPAVGWDDLVLPAPTHRRLRDLAVRARHRDQVLGQWGMRPGGGRGRGVIALFAGSSGTGKTMSAEVVAADLGMDLYVVDLSTVVDKYVGETEKNLERIFTEASAVNAVLLFDEADAIFGKRSDVKDSHDKHANMESAYLLQRMESFDGIAILTTNLRANLDEAFTRRLDVIADFPVPDAAQRRALWERCLGGRLPRADDVDLAFCADRFELAGGSIRACAVTAAYFAAASGEPLTMRQVMTAVAQEYRKLGRLVLEGEFGPYLGQVADV
>NZ_CP019798|4647861:4705525|4700982_4701327_-|WP_078094874.1|DBSCAN-SWA
MLRYLPFLLIIALTIYAFIDCLNTPEEEVKHLPKAMWVIIILLFSIVGPVVWLFAGKKRVVSGGGGRGPRGRSRWVAPDDNPEFLKSLREEQENKDRDRDNGKDQGKDQGKDAD
>NZ_CP019798|4647861:4705525|4693922_4695149_+|WP_078096290.1|DBSCAN-SWA
MRGVSRRGLLGLGLGAAAAMGVAGCGLPDVSGPGAPGPVKNPKPGEKTPARPIGDGSTADTGPQPHQPDRPVPLQPGETPPQFVVFSWDGAGEIGNGLFPRFLKLAKDHGAAMTFFLSGIYLLPESKRSLYQPPNNPVGASDIGYLKDENVRTTLRLVREAWLDGHEIGTHFNGHFCGGSGSVARWTPADWESEIDQAVSFVTNWRTHTGFTDVEPLPFDYRKELTGARTPCLLGRDNLLPTARKLGWRYDSSSPGGLQVWPVRRSGVWDLPLQSLPFPGHSFEVLSMDYNILANQSKNTTKGVPAHYPAWRAQATATYLGGFRRAYETNRAPLFIGNHFEEWNGGIYMDAVEEALKGMADKRDVRLVSFRQFTDWLEAQDPKVLARLRTLGPGQSPAGGWNAYLTAA
>NZ_CP019798|4647861:4705525|4660728_4661145_-|WP_030851932.1|DBSCAN-SWA
MATSTAAARREEARSAYDAFLKECPTGQLLARISDKWVGLVVSALGEADDRSMRYSDLGRKIPGVSQKMLTQTLRSLERDGLVTRHVTPTVPVRVDYRLTDLGSSLGNLLSSVKVWAENHFDEVSAHRDTYDRAAAAS
>NZ_CP019798|4647861:4705525|4704919_4705525_-|WP_076043870.1|protease|DBSCAN-SWA
MSTTVDTGWTQTDRAKAAAKLMLGWVALLWLLEAVDHATGHALDQYGIVARDPDSLGGIVSAAFLHFGFDHVASNSVPLLVLGFIAALSGIRRFLAVCGLILLADGLGTWLISPSGTMTLGASGIVFGLFGYLLVRGFVERRALGIAVAVGVAAVWGTTIVSGILPTDSGVSWQGHLCGLVAGIVTALYFRRPARRPAVTA
>NZ_CP019798|4647861:4705525|4702871_4703345_+|WP_078094875.1|DBSCAN-SWA
MSPIAVSGPELNLGTEEAYVVLARPKIDPTQPGVIAAAREAGVSPEEFAGPGDVWTLMYDADGDGDGFELPGARDTEADAFAEQVQQALAAAEPFTVEAGNFLRLDARPAGADWVVTAHVTPPEGEEDGAAARTLELGALPAADLLAELEQFRRGLA
>NZ_CP019798|4647861:4705525|4700613_4700931_+|WP_173675344.1|DBSCAN-SWA
MTGLAAPSRGSSELSTWQVDMPAGATGPEHSVSREQVWTLTAGSLEVTSDGRTQKVTTGQTLVLPADAPRRIHAAETFRAHVAMRADGVVSVPGEEEPRVLPWAR
>NZ_CP019798|4647861:4705525|4688421_4689135_-|WP_060181049.1|DBSCAN-SWA
MRCADNNSPSLNAGSGIPQPPAPAPPRRTGRRVTVAVYASDPILRVGVVHQLRQRPEIELVPDAEADAAQVSLVTVDSVDDETAALLYRLRHNPDTRTGLVVGTFESGDALQRAIECGVSAVLRRAEADQDRLLRLVLAIANGEGVLPGDLLAKLLDHMGSLQRSALDPRSVSLSTLTSREADMLRLVSEGLDTAEIARKTSYSERTVKNVLHEVITRLQLRNRTHAVGYALRNGLI
>NZ_CP019798|4647861:4705525|4701417_4702875_+|WP_030026270.1|DBSCAN-SWA
MAYDDLRSLLRALEREGDLKRIKAEVDPYLEVGEIVDRVNKAGGPALLFENVKGSAMPLAMNVFGTDRRLLKALGLKSYAEISEKIGGLLKPELPQGFIGVREAFGKLGSMVHVPPKKVKGDSAPVQEVVLTGDDVDLDLLPALFTWPKDGGSFFNLGLTHTKHPETGVRNLGLYRLQRHDKRTIGMHWQIHKDSRNHYAVAAAKGERLPVAIAFGCPPAVTYASTAPLPGDIDEYLFAGFVAGKRIEMVDCKTVPLQVPANAEVVVEGWLEPGEMLPEGPFGDHTGFYTPQEPFPALKIDCITMRKRPLLQSIVVGRPPTEDGPLGRATERFFLPLLKIIVPDIVDYHLPESGGFHNCAIVSIDKKYPKHAQKVMHAIWGAHMMSLTKLIIVVDKDCDVHDLHEVSWRALGNTDYSRDLTVVEGPVDHLDHASYQQFWGGKAGIDATKKLPEEGYTRDGGWPDMVESDPATAALVDRRWKEYGL
>NZ_CP019798|4647861:4705525|4663102_4664047_+|WP_159050814.1|DBSCAN-SWA
MNKRTRVVTAIAVVAVLTGSASACSEESPKDMETARRAQAALDSANEALDQEREAETKLIRKCMNDQGFKVFPSDGANSNKGGKRSEDLTPTSEAARTVGYGADPRRSENQKTQEAGDDFDALPEDVKRAHSMAMDGYVDKPEGGVEFDFGGGKVMVPSKGCRGETLKAVYGDVKEYLRLNWTVYNTVKQDSARILGDDDAYQKALSEWASCMKAGGYPEIPTPEKAREAALSHYANVPDGDTAALDNAQRAEIKQATTDADCGTKVGLNTKAREAKSKASADSLVKHEAEITAWLELITKAKAKAQELLRETS
>NZ_CP019798|4647861:4705525|4691749_4693072_+|WP_078094873.1|DBSCAN-SWA
MAGVSYPYPYEAPVSQTLFERASLVTPGGVNSPVRAFRAVGGTPRFMVSGTGPYLTDADGREYVDLVCSWGPMILGHSHPEVIEAVQAAVARGTSFGTPGEGEVALAEEIVARIEPVEQVRLVSSGTEATMSAIRLARGFTGRAKVVKFAGCYHGHVDALLAAAGSGLATFALPDTPGVTGAQAGDTIVLPYNDLEAVRAAFAAHPGEIACVITEAAPGNMGVVTPAEGFNQGLADLCRENGALYISDEVMTGFRTSRAGWYGVDGVKPDLMTFGKVMGGGFPAAAFGGRADVMGHLAPAGPVYQAGTLSGNPIATAAGLAQLRLLDAAAYEKVDAVSAEIQGLVTGALAKEGVAHRLQTASNMFSVFFTGDAVRNYDDAKKQESFRFNAFFHSMLAQGVYLPPSAFESWFVSTAHDEKAIERVAAALPAAARAAAEATA
>NZ_CP019798|4647861:4705525|4680256_4681816_-|WP_030855544.1|tail|DBSCAN-SWA
MPTYLTPGVYVEEVQSGARPIEGVGTAVAAFVGFAQSGPFHEPTLVTNWDQYSQHFGGFTEGTYLPHAVYGYFANGGGAAYVVRIGGPAADGSAPAAAGAVPQPRTAQPVELGGFLITARPGITGVSVEIADADGDNPPEDRFKLLVRQGEQIAETYEASSRKNVKGYLVTQARASKLIEVTEQRSATQTRPAGQTVALPDAPAAVAATTGQGAVARLDPAEYVGDAGARTGFAGLETIDEITMVAVPDLMSAYERGDIDAEGVRTVQLAVISHCEQMGDRVAVLDTPPALSAQQVRTWRNDEAGYDSRYATLYYPWVKVFDPASGRNTTVPPSGHVAGVWARSDAERGVHKAPANEVIRGAVDLELRLSKGEQDLLNPIGVNCVRAFPGRGIRIWGARTLSSDPAWRYLNVRRLFNYLEESILLGTQWVVFEPNDDRLWSSIRRNVTAFLTEEWRRGALFGRTAAEAFYVKCDRDNNPQESIDQGRVVCEIGVSPVKPAEFVVFRLAQFSDSTSLVDE
>NZ_CP019798|4647861:4705525|4676064_4679103_-|WP_078094869.1|DBSCAN-SWA
MAWRDRLRRRTAVPDAGASAPAAAAADGAAVPAAGPAVPGDWDGGWRMTAPPLLTVSRSVTGVSDGLAFRSGLAAWRNPSFDTGLAHGLLPSAPAGLVRGVARPATARPTHSGGGPLLLRALPGEPTGTGADQQPEQAGPARETPQVSRRARPGATAPTADRGADAGTPGPAGSRAEARGASSTSAASASAANSASPARARNRTRTQGSGSMAAAGTRGLTSTDSPAVLGASAPPVQRAAEPGRATAPAAFPVVRRIAVIPAPPAADGSAPVRAAADARPARTSGETPGADRTTAVRPRPVGRTLTTARVPATPRRRVAAVRPPALPAAGPDLPVQRAQTRAPLGAPPTELPPPAAPSTPPGPTAAAPMPMVQRQAESAASGPTAENPLRTRAPLGTPLTELPSPATPSPSHPAPASPGPAMPTVQRQAEPPTAGPATPAIPTVQRQAEASGPAAEKPMRTRAPLGTPPPATPSHPAPATPGPAKPTVQRAAEPSPTGPAMPTVQRQGETAASGPTAEKPMRTRAPLGRPLTELPPTATPSHPAPATPGPAMPTVQRQTEHATTSPAAPATPTVQRQAEPAASGPTPEKPMRTRAPLGAPLTELPPTATPSHPAPATPGPAMPTVQRAAEPATTSPAAPAIPTVQRQAETAASGPTADKPMRTRAPLGAPLTELPPTATPSNPAPATPGPAMPTVQRQTEHTTSSPAAPAIPTAEPAASGPVGRVAPRVRSGLGAPLPSLPTSAAVPRPAAARPQAPLLGGAAGGAHPRAAAPPVQRATAPRSSGPVPLVAARAVGGAAAAAPAAPPSLQLLAARPLALGTGDAAGLGSTPAASRPARRPVVPARWSAPSAAAPQPVQRASAPAAPAPVPRPARAVRPAPASAAAAATAAAPLPVTGPYTPPLVVQPAPAAPAAGSVPVVRPRASAPAAVPGPPLAGPPVPVPPPSGPPPPVQRDTGRAGRAGGGRDAAAHGGGDLDLDDLARRLLDPVARLLRTELRRGRERAGRPFDGRR
>NZ_CP019798|4647861:4705525|4667626_4668379_-|WP_076046166.1|DBSCAN-SWA
MPVAPRPVVRPLAVSDDVAGVPCPACGTPNPPDRRFCRRCAAPLTPSTIAAPLPWWRTVWPLRRRTRAGSGRLVRFLVVLTVVLALCAAGFLLLPAGQHLVQDTLDKLGKAKAVTPTRAQASAELPGHPVGLSTDGLSNRYWAAPGPGTSATYTFGKPFRLVAVIITNGASPAPEEYAKQGRALRIDMEVTDRDGATVHKQLVLSDKPGPQTFPTGISDVATVRLTLQEPAGSAPERPLALAEVEFFQRG
>NZ_CP019798|4647861:4705525|4685067_4688199_-|WP_060181050.1|DBSCAN-SWA
MLLLAPLLAVTAAAGPGDAGAQPLAADAGSSRVAYAGTRHRSLGRVANDKNDTSTPLFGDGPAHLDVQPSALGDLLVFASRRDEKNPQVYLRSADGSVRRLTSGMDAGNPRLTPDGRSVVFDSAQRGAAGGVQRDLWLVRTDGTGLTRLTDTPANEEHPTVSADGGRLAYSSDADRAAGAQVYVRPLRGGAATRLTDPANGRATEPVWNPVDDATNRDVIAYTATGASGPRLRWTNGRADGQLLAGAQAGWRTRGAAWLPDGDGLLFLSPDRTCDCKGDWDHVFQVPAHSADTPKLVYSEDREIGSPTWLGPLKGGGAVVERISAAGPHVVTLQDARMDGSDPRDLGLTILDEDPAADTNTDPAKDPLFQPGPDFDPWTERQNYTPDGRRIVVTRFEGKPGSRIQRIWTADADGTNAEALPLAGRGPKDWDTDPTFSPDGRYLAFTRTSPGGVGQAAGPSRILIADAATGAIRGEITPPADQPKGGDAQPTWSSDGTMLAFTRNLVINGHGGNKHIWTVPVDHLDRQRDLSATICFGACEVIDDSPAFSPDGTTVAFNRKNGAGRVDERSGILLASPAGGSCRVLLPDAARGKPGACGRELPETTGNGPYQPRDAAWTADGKSLVLTGRGSRAANSPEKLKLVDVATGAHNLLVTGLPGRQKEPSVQQSVDLAVRAPDKSAPLTVGGSATVRVDVVNQGPAASPGTRLTVAPPLGVGITALTVPGTPGATCDAAALTCTLGIVPPGTTVPVTATLTGLIPGDQPVEWSVTGTVLDPRPSDNAGRTVVPVREAPVPPKPTPTPTPPTPTPAPPTTPPTTPPPAPQPPAPQAGPGVGITAQPNPGYVGGRVVVTFTVANGRSALATGLRLRIGLPEGVPHDGPPPGCDRNWTCALADLAPGARTVLRVVLSPDKALTGQVTANLTTTGTDADPGDNTAREQLRILQPRIVAVPPIGRPGFVTSVRGEDFPPGAPVRFAWKPGITAAAAPTVPQADGTFIGQLLILAKDQTGPRIITASGPGFSPVQTDFLVVNGTVQPPDEVTRR
>NZ_CP019798|4647861:4705525|4695858_4696632_+|WP_060181046.1|DBSCAN-SWA
MVEYVLAAEATGVNETVLNGALLLAVPIALLAGLVSFFSPCVLPLVPGYLSYVTGVSGADLAEARRGRMLAGAALFVAGFTAVFVSTGALFGYFGSELQENKAIISRVLGALVIVLGLFFMGAIPGLTMREFRFHKKPTAGLLGAPLLGVLFGVGWTPCMGPTLAAVNTLSIDQASAGRGALLTVVYCLGLGVPFILAAIAFRKALGAFGWVKQHYAWVMRIGGGMLILTGLLLVTGLWDSIVTDMQAWTQSFTVGI
>NZ_CP019798|4647861:4705525|4669642_4670215_-|WP_030851951.1|tail|DBSCAN-SWA
MSRAAVPGLPSRHPIGGQLPALYADDDFAQRFTAGLDTVLAPVFTTLDNLPAYFDPRLAPADFLSWLASWVGGADDPDWPAALRREAVARAVELHRWRGTRRGLVEALRLVLGVSADVSGDGGAVWSRTAGTEPTPVAAGEVLVRVWPRGTNPAHGVDAERVHALVRALCPVHTVCRVEILPGPPAPEGS
>NZ_CP019798|4647861:4705525|4693068_4693767_+|WP_030855554.1|DBSCAN-SWA
MSAVGRDAKSDLTVVHLVRHGEVHNPDGVLYGRREGYHLSELGRRMADRVAEHLKGRDIAYVVSSPLERAQETAEPIAKAHGLDLATDSRLLEAENVFEGKTFGVGDGALRRPGNWKHLTNPFKPSWGEPYVEQVVRMMSALEAARDAARGHEAVAVSHQLPIWIVRSFAEKRRLWHDPRRRQCTLASLTSFTFQGDKLVSVGYSEPARDLVPAHLLAGAKPVKGASKAFGA
>NZ_CP019798|4647861:4705525|4674795_4675521_-|WP_030856159.1|DBSCAN-SWA
MASSARASRARAQLTLKEPPASVGAKPGGTIARLDLQFNPSTLQLGKTTEWRRSPSRMAGQSALPEFVGSGPRTLSLEVFLDATAKHDNSVEQAVEKLMKACVPTPASLGRKKPASPWVRFEWGSARTTSFDGVLSNLSVSYTLFDVDGKPLRATCSLSIEEASVDPPGQNPTSGSRTARSTHTVVAGDSLAMLAWREYGDATAWRVIAEANGIDDPMALVPGTEIVVPGTRDQHGEEEQR
>NZ_CP019798|4647861:4705525|4659957_4660686_-|WP_030851930.1|DBSCAN-SWA
MNGPGIQLTLAPELRLFAPPSRRADRVPTATDGASSLGHVVESAGVPLTEVGRLLVDGHEVPVSYVPQDGQSVEVFGVERPQQVPGAPLRFLLDVHLGTLARRLRLLGVDAAYENEDIGDPALATRSAAERRVLLSRDRGLLRRREIFAGAYIYSDNPDEQLRDVLGRFAPALAPWTRCTACNGPLHEADKESVGDRLEHGTHRSYDVFAQCAACERVYWRGAHHARLERIVDEALVEFGTA
>NZ_CP019798|4647861:4705525|4695227_4695854_+|WP_076043868.1|DBSCAN-SWA
MSLSRAPRRRSPSGRALLLTAVTVTGALTLTACGGSDSGKPTGSGGNYVTGASGISTAAEGERVEAPGLDGETVDGKPLDTAALKGKVVVLNVWGSWCPPCRAEAPSFAKVSKELADAGKDVVFVGVNVRDNSKQNAASFEETFGITYPSLYDPDGKQLLRFPKGSLSPNAIPSTLVLDREGRIAARTLAPLSEEQLRSMIDPVLAEQ
>NZ_CP019798|4647861:4705525|4675601_4676027_-|WP_030856157.1|tail|DBSCAN-SWA
MTDNIFATSVFFRLAIGGNDLGAFHTCSGMGAEVEMESYAEGGNNGFTWQLPGRVTWSNITLTRPVTTDTAKIGRWLDETLRRVEPKDGEIVALRPDLSRIIGWQVFGIVPVRWQGPSFDPANSAAAVETLEIAHQGLLPS
>NZ_CP019798|4647861:4705525|4659420_4659915_+|WP_030851928.1|DBSCAN-SWA
MVAVRRVAVRSVVVAGLLALGAGVPGPSQAWGSGWAGPEADVSYHGRVALAGSQLRVLLVPENDGPAALANATLRVRLSADLADRQQLPQGCAQAGLREVVCETGPLPLQGRGRHVGLALELRERVPEVVVRVDTWWNGGATDRNRANNEHVVLALDTGDTYAF
>NZ_CP019798|4647861:4705525|4658118_4658892_-|WP_030851923.1|DBSCAN-SWA
MSTAATRTAVVTGASSGIGAATARQLAAAGYHVVLTARRKDRIEALAAELTGAGHSATAHALDVTDRAAVDALAASLDRYPSVDVLVNNAGGAIGAEPVATGDPADWRTMYEVNVIGTLNVTQALLPALTASGDGTVVVLSSTAGHATYEGGAGYVAAKNGARVLAETLRLEIVGQPVRVIEIAPGMVRTEEFAKTRFRGDAEKAEKVYAGVAEPLTADDVADTITWAVTRPSHVNIDLLVVRPRAQASNTKVHREL
>NZ_CP019798|4647861:4705525|4670211_4672185_-|WP_060180880.1|plate|DBSCAN-SWA
MALPSPNLDDRRFQQLVDEAKRYVQQRAPEWTDHNVSDPGVTLIETFAYLVDQLLYRLNRVPEKNYLAFLDLLGIQLYPPSAASADVDFWLSAPQPDTVTLPAGTEVTTEVTTSAGDSEEAVVFATTGDLRILPSELTKLVTAPRTGEPADRTGALAEGRGIPCFQATPEPGDAVLFGLPTAVPRCIVAVRLDSRVEGVGVDPRQPPLVWEAWDGGRWQRCATDSDSTGGLNRPGEIIVYVPAGHTASVISGTRAGWLRCRVTEPEPGQPFYSESPTVREAAVFTVGGTMTVEHAERVSDVPLGASEGVAGQSFRLGRPPVLLDGEPPVVEVSSPEGWQRWDVVEHFGRSGPDDRHVRVDATTGEFSFPPVLREADGSLRACGAVPPKGSRIRVARYRTGGGPAGNVSRGAISVLRSSVPYIARVANREAARGGVAGETVDNAKLRAPEALRMQERAVTAEDYEIIARRAAPSVRRVRCLPATDGGRGAGSARVLVVPDAVADEGDRLRFEQLIPSDQVLAAITTALDERRLIGTGLVVEPPAYQGVTVVARLSAPAADADRIRDAALAALFRHLNPLHGGPDGTGWPFGRPVQYGEVFGVLQRAVGDVLVEEIRLFAADPITGRRGAPVDRIDIGAGTLVFSYQHQVVVAEPEVHG
>NZ_CP019798|4647861:4705525|4664054_4665581_+|WP_107499906.1|DBSCAN-SWA
MSLEHPEGPQAAEPSGGRARHRSRRALVIAAAVVVLFGSSGSVWWIASQARTPEQRASNAAAPPPSRITGKVSDQQLVEKMELTGKVETASRTTIAGVQPQGTSRAVVTGLPAAMGKTLKAGAVVAEVSGRPVLLLPGRFPAYRDLKAGDKGPDVQQLQRALQPLYGTAVNGTYGPATVEAVRKLYAAAGYEAPSGQGQSQGGGGAGGGGTGGGGAPSGASGGGSAPRGGAETDGGTGAAPRTKAGASAPPARGSDAPPGSGPAKAGELLPAAEVAYVSTLPATVVQVTAAVGDAADKPLVVLGSGGRQVRATLTADQRTRLRDLPDDAVIRFGTGPYEGREGSLGSLAGPADAKSGEQQGNAKTGGQEGAGTSGAAGTAGTAGGGGGNGASGGGGGGGGAGQHEALFVPSGAEAKEGAVQQISVELRRSPKGALTVPVSAVWTDLGGGSTVTVSDGGKERDVPVEVLFTHEGLTAVTALDANLGAGETVVLVRRGKTADGAEGGTDD

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_078094859.1|4647861_4649631_-|tRNA	arginine--tRNA ligase	M1PAX3	Moumouvirus	6.5e-77	31.9
WP_078094860.1|4649810_4651550_+|tRNA	lysine--tRNA ligase	NA	NA	NA	NA
WP_078094861.1|4651659_4653030_-	DUF2637 domain-containing protein	Q6VY65	Streptomyces_phage	4.1e-79	70.1
WP_051700584.1|4653154_4653919_-	DUF3558 domain-containing protein	NA	NA	NA	NA
WP_107052362.1|4654032_4654893_-	hypothetical protein	NA	NA	NA	NA
WP_078094862.1|4655125_4656319_+	RtcB family protein	A0A1I9SAD2	Rhodococcus_phage	1.1e-123	57.6
WP_078094863.1|4656396_4657215_-	hypothetical protein	NA	NA	NA	NA
WP_078094864.1|4657554_4657980_+	hypothetical protein	NA	NA	NA	NA
WP_030851923.1|4658118_4658892_-	SDR family oxidoreductase	NA	NA	NA	NA
WP_060180868.1|4658954_4659290_-	YnfA family protein	NA	NA	NA	NA
WP_030851928.1|4659420_4659915_+	hypothetical protein	NA	NA	NA	NA
WP_030851930.1|4659957_4660686_-	Mut7-C ubiquitin/RNAse domain-containing protein	NA	NA	NA	NA
WP_030851932.1|4660728_4661145_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_060180869.1|4661276_4662173_+	NADP-dependent oxidoreductase	NA	NA	NA	NA
WP_143568903.1|4662645_4663029_+	peptidase inhibitor family I36 protein	NA	NA	NA	NA
WP_159050814.1|4663102_4664047_+	hypothetical protein	NA	NA	NA	NA
WP_107499906.1|4664054_4665581_+	peptidoglycan-binding protein	NA	NA	NA	NA
WP_078094866.1|4665465_4666320_+	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	2.1e-28	40.4
WP_143568901.1|4666309_4667590_+	ABC transporter permease	NA	NA	NA	NA
WP_076046166.1|4667626_4668379_-	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_078094867.1|4669448_4669637_-	zinc-ribbon domain-containing protein	NA	NA	NA	NA
WP_030851951.1|4669642_4670215_-|tail	phage tail protein	NA	NA	NA	NA
WP_060180880.1|4670211_4672185_-|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_030851958.1|4672184_4672607_-	GPW/gp25 family protein	A0A1D8KT65	Synechococcus_phage	1.3e-07	30.8
WP_030851960.1|4672606_4672924_-	PAAR domain-containing protein	NA	NA	NA	NA
WP_078094868.1|4672981_4674799_-	VgrG-related protein	NA	NA	NA	NA
WP_030856159.1|4674795_4675521_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_030856157.1|4675601_4676027_-|tail	phage tail protein	NA	NA	NA	NA
WP_078094869.1|4676064_4679103_-	hypothetical protein	NA	NA	NA	NA
WP_167344733.1|4679107_4679266_-	hypothetical protein	NA	NA	NA	NA
WP_078094870.1|4679262_4679760_-	hypothetical protein	NA	NA	NA	NA
WP_030031999.1|4679756_4680197_-|tail	phage tail protein	NA	NA	NA	NA
WP_030855544.1|4680256_4681816_-|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	1.6e-66	32.9
WP_078096289.1|4682063_4684172_-	ATP-binding protein	A0A0R6PCP6	Moraxella_phage	2.4e-22	32.2
WP_078094871.1|4684366_4685071_-	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_060181050.1|4685067_4688199_-	PD40 domain-containing protein	NA	NA	NA	NA
WP_060181049.1|4688421_4689135_-	response regulator transcription factor	NA	NA	NA	NA
WP_060181048.1|4689388_4690672_+	hypothetical protein	NA	NA	NA	NA
WP_076043866.1|4691007_4691616_-	hypothetical protein	NA	NA	NA	NA
WP_078094873.1|4691749_4693072_+	glutamate-1-semialdehyde 2,1-aminomutase	NA	NA	NA	NA
WP_030855554.1|4693068_4693767_+	histidine phosphatase family protein	NA	NA	NA	NA
WP_078096290.1|4693922_4695149_+	hypothetical protein	NA	NA	NA	NA
WP_076043868.1|4695227_4695854_+	TlpA family protein disulfide reductase	NA	NA	NA	NA
WP_060181046.1|4695858_4696632_+	cytochrome C biogenesis protein ResC	NA	NA	NA	NA
WP_060181045.1|4696645_4698343_+	cytochrome c biogenesis protein ResB	NA	NA	NA	NA
WP_030855559.1|4698339_4699422_+	c-type cytochrome biogenesis protein CcsB	NA	NA	NA	NA
WP_060181044.1|4699447_4699963_+	SRPBCC domain-containing protein	NA	NA	NA	NA
WP_060181043.1|4699999_4700458_-	MarR family transcriptional regulator	NA	NA	NA	NA
WP_173675344.1|4700613_4700931_+	cupin domain-containing protein	NA	NA	NA	NA
WP_078094874.1|4700982_4701327_-	PLDc N-terminal domain-containing protein	NA	NA	NA	NA
WP_030026270.1|4701417_4702875_+	menaquinone biosynthesis decarboxylase	NA	NA	NA	NA
WP_078094875.1|4702871_4703345_+	hypothetical protein	NA	NA	NA	NA
WP_060181040.1|4703341_4704265_+	4-hydroxybenzoate octaprenyltransferase	NA	NA	NA	NA
WP_078094876.1|4704342_4704930_+	Uma2 family endonuclease	NA	NA	NA	NA
WP_076043870.1|4704919_4705525_-|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA