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_CP021768	Stenotrophomonas sp. WZN-1 chromosome, complete genome	11 crisprs	csa3,DEDDh,WYL,cas3,Cas9_archaeal,DinG	1	4	4	0

1. NZ_CP021768

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP021768_1

• CRISPR_ID: NZ_CP021768_1
• CRISPR_location: 126147-126246
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_1

Consensus_repeat	Method
GTGGGTGCCGACCGTTGGTCGGCAC	CRISPRCasFinder

spacers of NZ_CP021768_1

>1.1|126172|50|NZ_CP021768|CRISPRCasFinder
TTCTACTGTTCTGGTGGGTGCCAGGCTTGCCTGGCACTGCTCCTGCTCCG

CRISPR arrays and Neighbor proteins around NZ_CP021768_1

CRISPR arrays

The CRISPR arrays of NZ_CP021768_1

>merge|NZ_CP021768|1|126147-126246|CRISPRCasFinder
GTGGGTGCCGACCGTTGGTCGGCACTTCTACTGTTCTGGTGGGTGCCAGGCTTGCCTGGCACTGCTCCTGCTCCGGTGGGTGCCGACCGTTGGTCGGCAC

>NZ_CP021768|1|1|126147-126246|CRISPRCasFinder
GTGGGTGCCGACCGTTGGTCGGCAC	TTCTACTGTTCTGGTGGGTGCCAGGCTTGCCTGGCACTGCTCCTGCTCCG
GTGGGTGCCGACCGTTGGTCGGCAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087921113.1|127089_128250_+|transglycosylase	unknown	unknown	gnl|CDD|225377
NZ_CP021768.1|WP_087921111.1|121581_122376_-|undecaprenyl-diphosphate-phosphatase	unknown	unknown	gnl|CDD|234712
NZ_CP021768.1|WP_087921114.1|128967_129546_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_CP021768.1|WP_087921110.1|120683_121508_-|META-and-DUF4377-domain-containing-protein	unknown	unknown	gnl|CDD|379548
NZ_CP021768.1|WP_004134334.1|124326_124665_+|P-II-family-nitrogen-regulator	unknown	unknown	gnl|CDD|223424
NZ_CP021768.1|WP_139319639.1|135902_137132_+|hypothetical-protein	unknown	unknown	gnl|CDD|377670
NZ_CP021768.1|WP_004153533.1|122599_124009_+|type-I-glutamate--ammonia-ligase	unknown	unknown	gnl|CDD|181884
NZ_CP021768.1|WP_087921107.1|116217_117252_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|223506
NZ_CP021768.1|WP_087921116.1|131109_133530_+|DDE-type-integrase/transposase/recombinase	unknown	unknown	gnl|CDD|366234
NZ_CP021768.1|WP_087921112.1|124686_126117_+|ammonium-transporter	unknown	unknown	gnl|CDD|182630
NZ_CP021768.1|WP_014035514.1|128358_128652_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_049441968.1|133529_134531_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|99707
NZ_CP021768.1|WP_087921106.1|115418_116210_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl|CDD|153251
NZ_CP021768.1|WP_087924111.1|120058_120517_-|META-domain-containing-protein	unknown	unknown	gnl|CDD|377111
NZ_CP021768.1|WP_087924112.1|126287_127034_+|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl|CDD|225567
NZ_CP021768.1|WP_087921108.1|117308_119378_+|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|274350
NZ_CP021768.1|WP_087921117.1|134770_135790_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|379062
NZ_CP021768.1|WP_155760248.1|134543_134771_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_075675701.1|137806_138175_-|H-NS-histone-family-protein	unknown	unknown	gnl|CDD|376390
NZ_CP021768.1|WP_087921109.1|119388_120000_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	unknown	unknown	gnl|CDD|176643

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087921113.1|127089_128250_+|transglycosylase	gnl|CDD|225377	COG2821, MltA, Membrane-bound lytic murein transglycosylase [Cell envelope biogenesis, outer membrane].	1.66589e-115
NZ_CP021768.1|WP_087921111.1|121581_122376_-|undecaprenyl-diphosphate-phosphatase	gnl|CDD|234712	PRK00281, PRK00281, undecaprenyl-diphosphate phosphatase.	1.53991e-85
NZ_CP021768.1|WP_087921114.1|128967_129546_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	2.67001e-22
NZ_CP021768.1|WP_087921110.1|120683_121508_-|META-and-DUF4377-domain-containing-protein	gnl|CDD|379548	pfam14302, DUF4377, Domain of unknown function (DUF4377). This domain family is found in bacteria and archaea, and is approximately 80 amino acids in length.	1.41069e-26
NZ_CP021768.1|WP_004134334.1|124326_124665_+|P-II-family-nitrogen-regulator	gnl|CDD|223424	COG0347, GlnK, Nitrogen regulatory protein PII [Amino acid transport and metabolism].	3.60313e-56
NZ_CP021768.1|WP_139319639.1|135902_137132_+|hypothetical-protein	gnl|CDD|377670	pfam06527, TniQ, TniQ. This family consists of several bacterial TniQ proteins. TniQ along with TniA and B is involved in the transposition of the mercury-resistance transposon Tn5053 which carries the mer operon. It has been suggested that the tni genes are involved in the dissemination of integrons.	0.000933762
NZ_CP021768.1|WP_004153533.1|122599_124009_+|type-I-glutamate--ammonia-ligase	gnl|CDD|181884	PRK09469, glnA, glutamate--ammonia ligase.	0
NZ_CP021768.1|WP_087921107.1|116217_117252_+|alpha/beta-fold-hydrolase	gnl|CDD|223506	COG0429, COG0429, Predicted hydrolase of the alpha/beta-hydrolase fold [General function prediction only].	4.86172e-29
NZ_CP021768.1|WP_087921116.1|131109_133530_+|DDE-type-integrase/transposase/recombinase	gnl|CDD|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	2.15096e-08
NZ_CP021768.1|WP_087921112.1|124686_126117_+|ammonium-transporter	gnl|CDD|182630	PRK10666, PRK10666, ammonium transporter AmtB.	5.9043e-177
NZ_CP021768.1|WP_075675701.1|137806_138175_-|H-NS-histone-family-protein	gnl|CDD|376390	pfam00816, Histone_HNS, H-NS histone family.	9.09777e-21
NZ_CP021768.1|WP_049441968.1|133529_134531_+|AAA-family-ATPase	gnl|CDD|99707	cd00009, AAA, The AAA+ (ATPases Associated with a wide variety of cellular Activities) superfamily represents an ancient group of ATPases belonging to the ASCE (for additional strand, catalytic E) division of the P-loop NTPase fold. The ASCE division also includes ABC, RecA-like, VirD4-like, PilT-like, and SF1/2 helicases. Members of the AAA+ ATPases function as molecular chaperons, ATPase subunits of proteases, helicases, or nucleic-acid stimulated ATPases. The AAA+ proteins contain several distinct features in addition to the conserved alpha-beta-alpha core domain structure and the Walker A and B motifs of the P-loop NTPases.	0.000294668
NZ_CP021768.1|WP_087921106.1|115418_116210_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl|CDD|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	1.86678e-38
NZ_CP021768.1|WP_087924111.1|120058_120517_-|META-domain-containing-protein	gnl|CDD|377111	pfam03724, META, META domain. Small domain family found in proteins of of unknown function. Some are secreted and implicated in motility in bacteria. Also occurs in Leishmania spp. as an essential gene. Over-expression in L.amazonensis increases virulence. A pair of cysteine residues show correlated conservation, suggesting that they form a disulphide bond.	1.44728e-05
NZ_CP021768.1|WP_087924112.1|126287_127034_+|N-acetylmuramoyl-L-alanine-amidase	gnl|CDD|225567	COG3023, ampD, N-acetyl-anhydromuramyl-L-alanine amidase [Cell envelope biogenesis, outer membrane].	6.97657e-54
NZ_CP021768.1|WP_087921108.1|117308_119378_+|tetratricopeptide-repeat-protein	gnl|CDD|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	3.35105e-24
NZ_CP021768.1|WP_087921117.1|134770_135790_+|AAA-family-ATPase	gnl|CDD|379062	pfam13191, AAA_16, AAA ATPase domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily.	0.000933318
NZ_CP021768.1|WP_087921109.1|119388_120000_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein	gnl|CDD|176643	cd00865, PEBP_bact_arch, PhosphatidylEthanolamine-Binding Protein (PEBP) domain present in bacteria and archaea. PhosphatidylEthanolamine-Binding Proteins (PEBPs) are represented in all three major phylogenetic divisions (eukaryotes, bacteria, archaea). The members in this subgroup are present in bacterial and archaea. Members here include Escherichia coli YBHB and YBCL which are thought to regulate protein phosphorylation as well as Sulfolobus solfataricus SsCEI which inhibits serine proteases alpha-chymotrypsin and elastase. Although their overall structures are similar, the members of the PEBP family have very different substrates and oligomerization states (monomer/dimer/tetramer). In a few of the bacterial members present here the dimerization interface is proposed to form the ligand binding site, unlike in other PEBP members.	6.05441e-51

Protein sequences

>NZ_CP021768.1|WP_087921112.1|124686_126117_+|ammonium-transporter
MKMRLLTGWQARFHLVCLLMLLSALAAGAWPGSAHAQVQVSPLPSESVAVEPLQDPAAAAAAPAVAEAAAAYDRGDVAWMLTSTLLVLLMVVPGLALFYGGLVRSKNVLSVLSQILVVFSLVLLLWVSYGYSAVFSAGNPFFGSFTEFAFLKGFTPDSVGNTPIKGLPDYLFVAFQSTFAGITTALIVGAFAERIKFRAVLLFSALWFTLSYIPMAHIVWGGGYLGELGAIDFAGGTVVHINAGVAGLVAAWFVGKRLGYGQTALKPHNVPFTYIGAMLLWVGWFGFNAGSAAAADTVASLAFLNTVLATAAAVLGWTLVEAIGKGKPSALGAASGAVAGLVGITPACGTVGPLGAIIIGFVAGVVCVWGVTGLKRMLKVDDTADVFGVHGVGGIVGAILTGVFSAQSLGGTKPDLDIAHQVWVQVISVGLTVVWSAVVTTLILLVVRSVVGLRVTEEAERTGLDVTSHGESAYEA
>NZ_CP021768.1|WP_004134334.1|124326_124665_+|P-II-family-nitrogen-regulator
MKLISAIIRPFKLDEVREALSDAGVSGITVTEVKGFGRQKGHTELYRGAEYVVDFLPKIKIETVVTDERADAVIEAIQSSAGTGKIGDGKIFVTAVEQVIRIRTGEIGADAL
>NZ_CP021768.1|WP_004153533.1|122599_124009_+|type-I-glutamate--ammonia-ligase
MSVENVEKLIKDNQIEFVDLRFVDMRGVEQHVTFPVSIVEPSLFEEGKMFDGSSIAGWKGIAESDMVLLPDTASAYVDPFYADPTIVISCDILDPATMQPYGRCPRGIAKRAEAYLKSSGIAETAFFGPEPEFFIFDSVRFANEMGHTFFQVDSEEAAWNSGAKYDGANSGYRPGVKGGYFPVPPTDTLHDLRAEMCKTLEQVGIEVEVQHHEVATAGQCEIGTKFSTLVQKADELLRMKYVIKNVAHRNGKTVTFMPKPIVGDNGSGMHVHQSLSKGGTNLFSGDGYGGLSQLALWYIGGIFKHAKAINAFANSGTNSYKRLVPGYEAPVMLAYSARNRSASCRIPWVSNPKARRIEMRFPDPIQSGYLTFTALMMAGLDGIKNQIDPGAPSDKDLYDLPPEEEKLIPQVCSSLDQALEALDKDREFLKAGGVMSDDFIDGYIALKMQEVTKFRAATHPLEYQLYYAS
>NZ_CP021768.1|WP_087921111.1|121581_122376_-|undecaprenyl-diphosphate-phosphatase
MSDLLSALLLGILEGLTEFLPISSTGHLLIAQHWLGARSDFFNIVIQAGAIVAVVLVFRQRLLQLATGFGQRENREYVFKLGAAFLVTAVVGLVVRKAGWSLPETVSPVAWALIIGGVWMLLVEAYTARLPDRDQVTWTVAIGVGLAQVVAGVFPGTSRSASAIFLAMLLGLSRRAAAAEFVFLVGIPTMFAASAYTFLEMAKAGQLGSENWTDVGVAFLAAAVTGFVVVKWLMGYIKSHRFTAFAIYRIALGAALLLWLPSGS
>NZ_CP021768.1|WP_087921110.1|120683_121508_-|META-and-DUF4377-domain-containing-protein
MNRKLTLLLPLALMAACSQTPAPAGNGGDDVAPAAAKAADQQTLAHLDAQRLQSQHWLLQQATGADGKRIDALFAREDKPVTLDFADGRLSVSNTCNRMGGGYTLADGKLSVSAMASTLMACTDKALMALDEAVSSRLQGELKAEQDADGKLTLTNAKGDVLVFNPEPTAETRYGGAGETVFLEVAAKTEKCSHPLIPDYQCLQVREVKFDDKGLKQGEPGKFENFYGNIEGYTHEDGVRNVVRVKRYEVKNPPADAPSQAYVLDMVVESAIEK
>NZ_CP021768.1|WP_087924111.1|120058_120517_-|META-domain-containing-protein
MKHVLALIVAALLAMPADVAAASTPSTDQLEAHRWQLARATDAQGRRIDALFVRGRPPYTLRFQPGYMSQLNLCNQSSSTYHLQGNRLVLEGGIITTAACIRAEVAEQERVAGTMVNARAEMTLALDARGRLLLRNAHGDVLEFAPVSGTDE
>NZ_CP021768.1|WP_087921109.1|119388_120000_+|YbhB/YbcL-family-Raf-kinase-inhibitor-like-protein
MQLSSHSLTNGAPIDREFAAGDAAGFAPDRNPHLAWSDVPEGTRSFLLVCVDPDVPTVPETVGRTDMSVPRDQPRCDFVHWVMADIPASVQEIAAGSCSDGFVVKGRATPAGPAGSRQGLNDFTGWFAGNPDMAGDYLGYDGPYPPFNDERVHRYFFRVFALDVASLRLPARFTAADAYRAMHGHVLAEAALHGTYTLNPALG
>NZ_CP021768.1|WP_087921108.1|117308_119378_+|tetratricopeptide-repeat-protein
MQDQIIQALRQNEADQAVQLAQAWTRDEPGQAEAHRWLALALQQQGNAEDAMQALQQALQLAPDNAQLHLQHAGLLLALRQFDGAGEALTRTTGLDPNAFAAYLMQAHLAIGRNDFDEAQRLSTLASRVEPDHPELLTIDGMIALRRDDPDRALTLLSAANQAQPNDIRVLYALGFAYLGKNMLAFAEQAFRRVLELNPTIASLHGLVVQLAMRQGNLEAAAEAMQIALQQQGLDTPSMRRLAGELALRSGQPLQALEHLLPLLESLPDDRDVLQLLLMSWQRLGREDEARARLDAALEQHPQLHDLWLARLAVEEVGSATAAATVERWMDAMPGHLPALEARLRLHDMVGEHTQAEAIAERIVSLEPGRVSGETRLVEGLLQRDPAAAVARVQALIDMAPEGHRADLRTWLGEIQDRAGQHEDALQTWLALQADQASQRLPLPPQAKAPPSWPDKGEIDGDATSAPIFLWGAPGSGVERVATGLAAASPVLRSDRYTSNAPDDAFQNYHTLQDLASGVLTPERLVQRWREQLPSRGVQDDAVIDWLLWWDNALLWALRPQLPQGRLLVVLRDPRDMLLDWVAYGAAAPLAMTSLAEASEWLARALAQVAALHEDDLYPQVLLRIDHIGNDPQAMADLLGRLFERPMPPAAQLGAPRFPPGHWRNYRDVMSAAFAKLTPIAVRLGYPEE
>NZ_CP021768.1|WP_087921107.1|116217_117252_+|alpha/beta-fold-hydrolase
MALIPPPVPDAGTPTLHAADYQPPRWLRNPHLQSMLSSSRMRLQRGLLLLAATGAISEELILDGGDGVRLQGWHSHVEGREPKGMALLLHGWEGSAESSYMRMAAARMLEQGFDVVRLNFRDHGNTHHLNPGIFHSNLIDEVVHAAGDIAQRWPQLPLVAAGYSLGGNFVLRLALRAPAAGVPLLRVASVCPVLDPALTMESIENGPAMYDWYFRRKWAGSLRRKRDLFPELSDCDDRVLKLDIRALTAWLVERHTSFGSLQAYFDGYSIAGDRLSTLQVPADILMAQDDPVIPYATFSDWQLPRQAHLETACWGGHCGFLENWRGDGFSERWVAQRLQRVLQG
>NZ_CP021768.1|WP_087921106.1|115418_116210_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MTSPTPAPRGGVARVCRYLYRVPLLLVHIVVFLPLILIGMLRPWGELRVGEATFGAKVVNWWQGGLMWIFGFRLVQIGRPLSGAVLFVANHVSWVDICILHSQRMMGFVAKREIASWPLVGWLAARGQTIFHQRGNTESLGGVMQVMADRLREGKAVGVFPEGRTRGGHEVGPFHARIFQAAVETGVPVQPVALVYGVKGDAQTIVAFGPGESFFANFLRLLGEPARRAEVHFLAPIGAQDLEGRRRIAETSRARIVAAMSTQ
>NZ_CP021768.1|WP_087924112.1|126287_127034_+|N-acetylmuramoyl-L-alanine-amidase
MHPTRTALMLSACLLLAACASTPQETRNPLATWVPSPNQNARTPVIIVIHHTEQKSVQQSLRTLRTANSGGPVSAHYLIGADGHRYQLVADERRAWHAGAGRWGTITDLNSASIGIELDNDGRSPFSAAQIESLIVLLRDLTTRLNIPPRQVIGHADLAPTRKQDPSRFFPWQQLAEAGFGVWPRAADGAAPEGFDAWNALARFGYPLDNRDATVAAFHRRFRGRDDLPKTLDAEDARILHSLLLQMP
>NZ_CP021768.1|WP_087921113.1|127089_128250_+|transglycosylase
MTESAFFSKHKHWALLAIVLLAGCATTGTGPEAPAAAKPAAATYAKVDWKTLPAVSDADLQAGFIAWRSSCTRLKNDAVWAKSCATAAAVSDKDPAAIRQFLQRDLEAYALRAGGHQADGLITGYYEPIYPGSLTRTDKATVPVYGTPDDLVVVQLDSLYPELKGKRLRGRVEGKVLKPYDDAGTIAAKGAKAPVLAWLTDPMDLQLLQIQGSGRVRLADGTQVRLAYAEQNGHPYRAIGRWLVDQGQLKKEDVTMDAIRAWARANPARVPELLRSNPSYVFFVRNPDSPEGPRGSLNVPLTAGYSVAVDRTVVPLGSLLWLSTTRPDGTPVVRPVAAQDTGGAIAGEVRADLYWGSGDAVGKLAGDMKQKGNIWMLWPKGMALPN
>NZ_CP021768.1|WP_014035514.1|128358_128652_+|hypothetical-protein
MKNIKNNNAKKYYKHWAESGLGKGNVLMEARGEKIVRQVEIYGTKMVWADEHAHSDDRFLLADQPVSFLDFDEDDEISAREFESAWKKAREATGYPV
>NZ_CP021768.1|WP_087921114.1|128967_129546_+|histidine-phosphatase-family-protein
MLVIVRHAQSMANAGFATADPESIALTAAGEEQARALAMTWSAAPDRIFTSPFLRARQTSQPLAERFKMVVAPLGVHEFTYLSPERCVGTSAADRKKWVEDYWSRCDPNYVDGPGAESFAQLVARAARALRILKSYSAHEQVVVFSHGQLMQAMRWICGSKAPSVVNAAAMGAFRKLDLDQPIAHCQRVSFE
>NZ_CP021768.1|WP_087921116.1|131109_133530_+|DDE-type-integrase/transposase/recombinase
MSTDAQSDGLSFEDRHQLYTRIKASELSIRQIESMVAGSGTKTVGKAALRNVRVRHNSIRNGGARTVESHTCELVFAYELELDPEVLGYYVQVPCRRVQRTTASGRNHISTAHVDFLVFRRDHVELVECKPLSWLESQLGLPDSLWVKQDAVWTYLPYAQWAQQHGLVFRVWVPPTPTGVYLQNLEACYAVAGDALQQHETTAVSKAARIIAKRPVLLDSLLTEVPGFTPRLALWMLGRSAAFGPLQSTPVARTDRFHLYGTKEQAKEADGLLFGAIVKGQSQPAVDDPLLVATATDLQRARQRLSRLALIEAGSLPATRRMGALQRQVRKAVAEGRSALSACLTKYAFSGNRASRLLPEHEQAIETVIALHWNTGRVHRPKDLLYVFEEECLRLGVEPCGRGRLDARRRSESPTRHALSTGGFRAYHATRTRTDPRHRSLPPIGYGHTLHVDASDLDVRCAPNLIHCFPASKAKFYIGIDGATGYPMAHALVFGSARTDALALLMREYVKRQGFLPKLIHLDRGPENTSRWLQDFCHGEISLRFSPTAGSAWNGIAENAIKQVNEQVAQRFQGSTRPDQMGRKVDGKFKSRNNARTDFVRVHEEFLNFVYHDLPMTPGPDDTTPIERRADALAAYGALGTPCEWNDGFLIRTSIKVEIKKRIDRQRGVRTIDGWFTSDELLQELRTEDASEVRSDCCDPNVIYVKVHGNWFKAFHNKVQSDALLSDQERLFHLLWAPSLRSQSAKRKEEVARARHSRRVQAQAARPATEHLAPVPMTGSDERLDIEPVPPAIAQDIVPFDEREDY
>NZ_CP021768.1|WP_049441968.1|133529_134531_+|AAA-family-ATPase
MKMVQHPAYEGPRKRLRMALDRHRPGHMVFIIGPSGVGKTTMRRSVMQEMFGNPACWDCGRIPLVETFATLPHGAYFSSRQLAVSILQELHAPTLAWLLDGSYLGEDAKLRIRRELAAATSEWASLARTRQTEGEYWGMVQRSLRARSCKYVSIDQVTALLVNHRDKSPADHTLHLMAIAEATGVMFVMTGVHKATQLWSVNSELRRRVTTVWVPPYSDKRRDDKLPFLRLLKSLATRYGLSQDDLLIRMANDILAATGGVFAEVVELLGRADIAAKQEGCNRILKRHIEISYYGSEDLRNLWRDIDAFEMSMVAGSVTERSEHVKARWGSPT
>NZ_CP021768.1|WP_155760248.1|134543_134771_+|hypothetical-protein
MTTDSNQFRWGADARRRRDDLARKLHARRRFAAALIIAIALLSHLAELAESTSHEGQDIGPSQEGVEALDKAEDF
>NZ_CP021768.1|WP_087921117.1|134770_135790_+|AAA-family-ATPase
MELLQHSAYRRPRDRLRAALDNHRPGHMVYVIGPSGVGKTTMRRSVMREMFGNPNLWEKGKVPAIETFACLPVGAYFSSRYLARELLQELNAPTLTWALEGRSPRSIPPSDIQAEVRDRDLQLGRYQLRLTEAECWSSVTRSMIARDCKYVAIDQISALLVNHKDKSPADHALHLMTLAESAGSMLIMSGIHRAVQLWSIGSELRRSVTSIWVPPYSVRRKEDRAPFLRLLMSLSERHNFSKQDLLIRMAADLLVATGGVYGEVAQLLSRAADAAKQEGSERILKRHIEASYYSDNDLANLWRDIEEFEDAMEAGSVTARAKQLKSSWASSYGEVCREV
>NZ_CP021768.1|WP_139319639.1|135902_137132_+|hypothetical-protein
MTMANMMSIVGPAIAGGRRGQVMGSGKYCGPSRDFSHRISTLKMLTAQDDLQCGTFWVLEDVLATYGGGRDTTRRRWCPVCYRDWDDDLSYEPLSWIVDIQAECDLHKCKLETTCSRCGADQPSSTDYQRRRRCHKCKQSLSGDGAAAAITGDEAWGQQQLASIIELCATPSQPQIPFENYVRFVKLLVDGHPMRRAYPNALKAEFYRATKNLSRGRTTIRAIVNLCALQSISARDILLSPDAAASEPLLDLWFSYATLKLPVGRHAERLERCAKCFSDVLKASEKDHYVPQMKVVLRRFRLNRQLLREMHLDVYEEYKLRYEEQGPYSQRVHLNRAMDLALQMVEGDADQAGSHRKLQQAAKQIGQRCNVSLDVGFSVMLGARNVLKALSENRLRKQPSGGRRRHSVA
>NZ_CP021768.1|WP_075675701.1|137806_138175_-|H-NS-histone-family-protein
MTIDISGLSAKELRSLIAQAEKQQSKVLSRPKATAMRAKINKYVKDHGYTIEELYGASVIVPSETAKKRGDRRSAKSTVPNTAPKYRNPAVRGQTWSGRGRQPRWIAELVASGKSLNDFLIK

Crispr_ID: NZ_CP021768_2

• CRISPR_ID: NZ_CP021768_2
• CRISPR_location: 777479-777625
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_2

Consensus_repeat	Method
CACGCATGGCGTGGCTCTACTGCCTCCATCGGCAGTGCAGTGTCGCATCC	CRISPRCasFinder

spacers of NZ_CP021768_2

>2.1|777529|47|NZ_CP021768|CRISPRCasFinder
CTAGATCCACGCCATGCGTGGATGGCGGGGACGTTGGGGAAGGCAGT

CRISPR arrays and Neighbor proteins around NZ_CP021768_2

CRISPR arrays

The CRISPR arrays of NZ_CP021768_2

>merge|NZ_CP021768|2|777479-777625|CRISPRCasFinder
CACGCATGGCGTGGCTCTACTGCCTCCATCGGCAGTGCAGTGTCGCATCCCTAGATCCACGCCATGCGTGGATGGCGGGGACGTTGGGGAAGGCAGTCACGCATGGCGTGGCTCTACTGCCTCCATCGGCGGTGCAGTGTCGCATCC

>NZ_CP021768|2|2|777479-777625|CRISPRCasFinder
CACGCATGGCGTGGCTCTACTGCCTCCATCGGCAGTGCAGTGTCGCATCC	CTAGATCCACGCCATGCGTGGATGGCGGGGACGTTGGGGAAGGCAGT
CACGCATGGCGTGGCTCTACTGCCTCCATCGGCGGTGCAGTGTCGCATCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087921560.1|784422_786579_+|TonB-dependent-hemoglobin/transferrin/lactoferrin-family-receptor	unknown	unknown	gnl|CDD|273808
NZ_CP021768.1|WP_075675352.1|764444_765890_-|adenosylhomocysteinase	unknown	unknown	gnl|CDD|377487
NZ_CP021768.1|WP_087921557.1|779782_780214_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087924131.1|762053_763397_-|peptidoglycan-binding-protein	unknown	unknown	gnl|CDD|366659
NZ_CP021768.1|WP_087921555.1|776376_777435_+|metal-dependent-hydrolase	unknown	unknown	gnl|CDD|377294
NZ_CP021768.1|WP_087924132.1|778639_779635_-|tRNA-dihydrouridine-synthase-DusB	unknown	unknown	gnl|CDD|129820
NZ_CP021768.1|WP_014036006.1|771552_772059_-|acyl-CoA-thioesterase	unknown	unknown	gnl|CDD|224523
NZ_CP021768.1|WP_010481882.1|772197_773409_-|methionine-adenosyltransferase	unknown	unknown	gnl|CDD|235374
NZ_CP021768.1|WP_087921552.1|768773_771485_+|phosphoenolpyruvate-carboxylase	unknown	unknown	gnl|CDD|234570
NZ_CP021768.1|WP_087921562.1|787256_788192_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087924133.1|784035_784230_+|hemin-uptake-protein-HemP	unknown	unknown	gnl|CDD|378463
NZ_CP021768.1|WP_087921558.1|780363_781329_-|ribokinase	unknown	unknown	gnl|CDD|238579
NZ_CP021768.1|WP_087921550.1|763447_764233_-|hypothetical-protein	unknown	unknown	gnl|CDD|226868
NZ_CP021768.1|WP_087921551.1|766130_768647_+|S9-family-peptidase	unknown	unknown	gnl|CDD|224423
NZ_CP021768.1|WP_087921554.1|775456_776257_+|UDP-2,3-diacylglucosamine-diphosphatase	unknown	unknown	gnl|CDD|277343
NZ_CP021768.1|WP_087921553.1|773744_775460_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|153248
NZ_CP021768.1|WP_014036013.1|781354_782653_-|nucleoside-transporter-NupC	unknown	unknown	gnl|CDD|224883
NZ_CP021768.1|WP_087921559.1|782847_783819_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381369
NZ_CP021768.1|WP_087921561.1|786583_787183_+|Hemin-transport-protein	unknown	unknown	gnl|CDD|226243
NZ_CP021768.1|WP_087921556.1|777695_778523_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|181382

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087921560.1|784422_786579_+|TonB-dependent-hemoglobin/transferrin/lactoferrin-family-receptor	gnl|CDD|273808	TIGR01786, hemoglobin-haptoglobin-binding_protein, TonB-dependent hemoglobin/transferrin/lactoferrin receptor family protein. This model represents a family of TonB-dependent outer membrane receptor/transporters acting on iron-containing proteins such as hemoglobin, transferrin and lactoferrin. Two subfamily models with a narrower scope are contained within this model, the heme/hemoglobin receptor family protein model (TIGR01785) and the transferrin/lactoferrin receptor family model (TIGR01776). Accessions which score above trusted to this model while not scoring above trusted to the more specific models are most likely to be hemoglobin transporters. Nearly all of the species containing trusted hits to this model have access to hemoglobin, transferrin or lactoferrin or related proteins in their biological niche. [Transport and binding proteins, Cations and iron carrying compounds, Transport and binding proteins, Porins].	6.4374e-130
NZ_CP021768.1|WP_075675352.1|764444_765890_-|adenosylhomocysteinase	gnl|CDD|377487	pfam05221, AdoHcyase, S-adenosyl-L-homocysteine hydrolase.	0
NZ_CP021768.1|WP_087924131.1|762053_763397_-|peptidoglycan-binding-protein	gnl|CDD|366659	pfam01471, PG_binding_1, Putative peptidoglycan binding domain. This domain is composed of three alpha helices. This domain is found at the N or C-terminus of a variety of enzymes involved in bacterial cell wall degradation. This domain may have a general peptidoglycan binding function. This family is found N-terminal to the catalytic domain of matrixins. The domain is found to bind peptidoglycan experimentally.	7.41664e-14
NZ_CP021768.1|WP_087921555.1|776376_777435_+|metal-dependent-hydrolase	gnl|CDD|377294	pfam04307, YdjM, LexA-binding, inner membrane-associated putative hydrolase. YdjM is a family of putative LexA-binding proteins. Members are predicted to be membrane-bound metal-dependent hydrolases that may be acting as phospholipases. It is a member of the SOS network, that rescues cells from UV and other DNA-damage. Expression of YdjM is regulated by LexA.	5.16004e-26
NZ_CP021768.1|WP_087924132.1|778639_779635_-|tRNA-dihydrouridine-synthase-DusB	gnl|CDD|129820	TIGR00737, Probable_tRNA-dihydrouridine_synthase, putative TIM-barrel protein, nifR3 family. This model represents one branch of COG0042 (Predicted TIM-barrel enzymes, possibly dehydrogenases, nifR3 family). This branch includes NifR3 itself, from Rhodobacter capsulatus. It excludes a broadly distributed but more sparsely populated subfamily that contains sll0926 from Synechocystis PCC6803, HI0634 from Haemophilus influenzae, and BB0225 from Borrelia burgdorferi. It also excludes a shorter and more distant archaeal subfamily.The function of nifR3, a member of this family, is unknown, but it is found in an operon with nitrogen-sensing two component regulators in Rhodobacter capsulatus.Members of this family show a distant relationship to alpha/beta (TIM) barrel enzymes such as dihydroorotate dehydrogenase and glycolate oxidase. [Unknown function, General].	9.41604e-147
NZ_CP021768.1|WP_014036006.1|771552_772059_-|acyl-CoA-thioesterase	gnl|CDD|224523	COG1607, COG1607, Acyl-CoA hydrolase [Lipid metabolism].	1.56219e-63
NZ_CP021768.1|WP_010481882.1|772197_773409_-|methionine-adenosyltransferase	gnl|CDD|235374	PRK05250, PRK05250, S-adenosylmethionine synthetase; Validated.	0
NZ_CP021768.1|WP_087921552.1|768773_771485_+|phosphoenolpyruvate-carboxylase	gnl|CDD|234570	PRK00009, PRK00009, phosphoenolpyruvate carboxylase; Reviewed.	0
NZ_CP021768.1|WP_087924133.1|784035_784230_+|hemin-uptake-protein-HemP	gnl|CDD|378463	pfam10636, hemP, Hemin uptake protein hemP. This is a bacterial family of proteins that are involved in the uptake of the iron source hemin.	4.0259e-16
NZ_CP021768.1|WP_087921558.1|780363_781329_-|ribokinase	gnl|CDD|238579	cd01174, ribokinase, Ribokinase catalyses the phosphorylation of ribose to ribose-5-phosphate using ATP. This reaction is the first step in the ribose metabolism. It traps ribose within the cell after uptake and also prepares the sugar for use in the synthesis of nucleotides and histidine, and for entry into the pentose phosphate pathway. Ribokinase is dimeric in solution.	9.21026e-99
NZ_CP021768.1|WP_087921550.1|763447_764233_-|hypothetical-protein	gnl|CDD|226868	COG4461, LprI, Uncharacterized protein conserved in bacteria, putative lipoprotein [Function unknown].	3.43476e-07
NZ_CP021768.1|WP_087921551.1|766130_768647_+|S9-family-peptidase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	1.24586e-56
NZ_CP021768.1|WP_087921554.1|775456_776257_+|UDP-2,3-diacylglucosamine-diphosphatase	gnl|CDD|277343	cd07398, MPP_YbbF-LpxH, Escherichia coli YbbF/LpxH and related proteins, metallophosphatase domain. YbbF/LpxH is an Escherichia coli UDP-2,3-diacylglucosamine hydrolase thought to catalyze the fourth step of lipid A biosynthesis, in which a precursor UDP-2,3-diacylglucosamine is hydrolyzed to yield 2,3-diacylglucosamine 1-phosphate and UMP. YbbF belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	2.96791e-70
NZ_CP021768.1|WP_087921553.1|773744_775460_+|GNAT-family-N-acetyltransferase	gnl|CDD|153248	cd07986, LPLAT_ACT14924-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: Unknown ACT14924. 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 uncharacterized phospholipid/glycerol acyltransferases such as the Pectobacterium carotovorum subsp. carotovorum PC1 locus ACT14924 putative acyltransferase, and similar proteins.	2.23999e-56
NZ_CP021768.1|WP_014036013.1|781354_782653_-|nucleoside-transporter-NupC	gnl|CDD|224883	COG1972, NupC, Nucleoside permease [Nucleotide transport and metabolism].	6.65968e-143
NZ_CP021768.1|WP_087921559.1|782847_783819_+|aldo/keto-reductase	gnl|CDD|381369	cd19143, AKR_AKR6C1_2, AKR6C family of aldo-keto reductase (AKR). Voltage-gated potassium channel subunit beta (KCAB) from Arabidopsis thaliana and Egeria densa are founding members of aldo-keto reductase family 6 member C1 (AKR6C1) and C2 (AKR6C2), respectively. KCAB, also called Shaker channel b-subunit, or K(+) channel subunit beta, or potassium voltage beta 1, or KV-beta1, or KAB1, is a probable accessory potassium channel protein which modulates the activity of the pore-forming alpha subunit.	0
NZ_CP021768.1|WP_087921561.1|786583_787183_+|Hemin-transport-protein	gnl|CDD|226243	COG3720, HemS, Putative heme degradation protein [Inorganic ion transport and metabolism].	0.00101592
NZ_CP021768.1|WP_087921556.1|777695_778523_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|181382	PRK08317, PRK08317, hypothetical protein; Provisional.	5.88792e-27

Protein sequences

>NZ_CP021768.1|WP_087921555.1|776376_777435_+|metal-dependent-hydrolase
MDSLTQIVLGGAVAAAIAPPGHRRAALLAGAALGTLPDLDALWLGFTAADPVANMIEHRSFSHSLLVLPWVAALIWWLFKRFGNGRVAQSPVRWFWAIQLALVTHPVLDAFTVYGTQLWWPLRPHPTMGSSVFIIDPGYTVWLLLGCVLAWFGRARPWAGKVLGVALLFSSGYLGWGLIAKAQVDRAAQQSLAAMGLGDAPRFSVPMPFNTLLWRVVAMTPNGYVVGDRSLLADDGPMRFEGHASNVQALREAQAIPAVQQLQWFNRGFMRAQVVDGRLLLSDLRMGLEPDYTFNFVVAEQAGGQWRPITPGQVRVDYSSPAARADAGRRLAAMWQRIWQQPAVSATGAAHP
>NZ_CP021768.1|WP_087921554.1|775456_776257_+|UDP-2,3-diacylglucosamine-diphosphatase
MSTLANLSPHRRAVFVSDVHLGSRHCHATELARFLSQLRCERLYLVGDIIDLWWMAHRRANWRQSHSEVIQALHALRRAGTEIIYIPGNHDASLRHVCGLMLPAMQVRRRAIHVTADGRRLLVAHGDEYDGVTHFGGLQEKFGDWLYYRILTGNQALNVVRRRLGMRYWSLSEFLKKRSGAAERYIERFVQAGLDDVRRRGLDGIVCGHIHRAALIERDGLVYANDGDWVESLTALAEDHDGALRLLDHNGQTLVELPGARLSQVA
>NZ_CP021768.1|WP_087921553.1|773744_775460_+|GNAT-family-N-acetyltransferase
MQELEQRLQQRFPDWFHGRRGQLARPLLRSVGRWSRLDQIEAFLQRSSGLRGFGFVAAGLEFIDGQYQVDPAALARIPATGRLLIVANHPSGARDALALLDAVGRIRRDVRIVANDLLGAIAPLQDLLLPVRILGGKAQRGSLHAVEEALAAEQCVIVFPAGEVSRLSLRGIRDGRWQRGFVRFARGAGAPVLPVRVEARNSALFYGASTLFKPAGTALLAREMFTRRGRPLRLSIGEPMQLGKGGDPGAQLLAVRRALYALGRTGAAGNAAACAGPEPLAAPVPPSQVAAGIAAATQLGQTADGKQILLATCTADSPLLLELGRLRELTFRQVGEGTGRSRDLDDYDPQYEHIVIWDAAAQRIAGAYRIMRGAQALARHGLSGLYSASLFRYSDDAITHIAEGLELGRSFVVPDYWGSRSLDYLWQGIGAYLQCRPGIRYLFGAVSISAALPRDAREQLVAYYQRYYSGTAGLAESNRPFQYFAAPPSFGELDAGAAFDVLKANLAALGTGVPTLYRQYTDLCEPGGARFLAFGVDPDFSDSIDGLIEVDLCAIRPNKRKRYLRDAGTPA
>NZ_CP021768.1|WP_010481882.1|772197_773409_-|methionine-adenosyltransferase
MSSYLFTSESVSEGHPDKVADQISDAVLDAILTQDQRARVACETMVKTGVAIVAGEITTSAWIDLEALTRKVITDIGYDSSDVGFDGATCGVLNLIGKQSPHIAQGVDRKKPEEMGAGDQGLMFGYATNETDSYMPAAIHLSHRLVEQQAKIRKKKNSPLSWLRPDAKSQVTLRYENGVVSAIDAVVLSTQHAPGIKQKDLIEAVREEIIKPVLPAKWLHKGTKFHINPTGKFEIGGPVGDCGLTGRKIIVDTYGGWARHGGGAFSGKDPSKVDRSAAYAARYVAKNVVAAGLADRCEVQVSYAIGVAEPTSISVTTFGTGKISDDKIEKLIRKHFDLRPYGIIKMLDLVHPMYQQTAAYGHFGRKPKEFSYLNGEGETVNATAFSWEKTDRAAALRADAKLK
>NZ_CP021768.1|WP_014036006.1|771552_772059_-|acyl-CoA-thioesterase
MSTELKTHQLSMTVLMSPEMANFSGKVHGGAILRLLDQVAYACASRYAGSYVVTLSVDQVMFRQPIAVGELVTFLASVNHTGTSSMEIGIKVVAEDILKRSVRHANSCFFTMVAVDEEGRPTPVPPLQPVTSDEKRRQAAALIRRQLRQEMEQRHLELLASNPPSPEE
>NZ_CP021768.1|WP_087921552.1|768773_771485_+|phosphoenolpyruvate-carboxylase
MNEYRSSIEFASPDLPLRDDVRRLGALVGDLLVEQVSAAFLDDVEDVRTRAIARRENQAPLSELADGLAGRTPQQAETMVRAFSTYFQVVNIAERVHRIRRRRDYQRAGTAGAQPDGLQDALQHLKAQGVGMDELALWLPRIDIEPVFTAHPTEAVRRALLEKEQLMVASLVDNLDGQRTPGEAAADAARFRMALTASWQTTDSSPVRPTVDDEREHVGFYLVQVLYRVIPVLYESLQQALRDTYGEELPLPRLLRFGTWVGGDMDGNPNVDAHTIRNTLDAQRQAVLGRYQKELLQLASLLSQSTERVGVSDALQARVVQYQQLLPQVQSRPRHADMPYRLLNDRMRARLQATLDDGEGAYAGPDELIDDLQLILDSLRANRGEHAGGFAVQRLLWRVKTFGFHLARLDVRQESSVHARALAIVLGGDTAWDGLDALGRAHLLAPHASGDTPLPKGDDEGNRRLDAVFAALADARARHGGDALGSYIISMAHDRSDVLAVLALARRGGLVGEGDTVPLDIAPLFETVDDLKRGTATLRDLLADPVYRAHLHARDDVQMVMLGYSDSSKDGGIAASRWGLQRAQVELLEVAAEAGIRLTFFHGRGGSISRGGGKTTHAVDASPRGSIDGRLRVTEQGEVIHRKYGIRALALRSLEQATGAVLRASLRPRAAEPREDDWRPVMDAVASASSEVYRAFVGQAGFMDYFRTATPIDVIERMTLGSRPSRRLGQDAALGNLRAIPWVFAWSQARAVIPGWYGVGSGLQAAVDAGHEQTLRDMARDWPFFRTFLDDIAMVLSKGDITIAEQFSLLSGDLHERFFPQVQRELELTRHWLLALMDQQTLLDHDARLALSIRLRNPYVDPISVLQVDLLQRWRASGREDDDLLRALVACVNGVSQGVQNTG
>NZ_CP021768.1|WP_087921551.1|766130_768647_+|S9-family-peptidase
MSMHARRTRRWTGLVLSMGLLAVAPLAWAAAPQPAAAQAPGVNGYELPSAALQAVVDAPRAPSLYLSPRRDVAALMQMPSLPSIQVVAQPELKLAGLRINPRTFSDSRFSFGEKLWLMNVADGKERQISGLPAKLSIASVMWSPDQKWLAFNQVDAASGANELWLVDVAGGSARRLVAGMNTVIGSGYQWLPDSRGLVVFTRPANLGAAPAADGIPTGPAVQQTRQGEGVVSIRTYQDLLKNEADARQFDYYATTQPVEVSLDGNTRAIGAAGIFMGFAVSPDGRFVLRQPVQRPYSYVVPVSSFPRRIEVIDRASGKLVHTVAVRPLVEGLPTGNDAEVTGVRDISWRGDAEATLVWAEAQDGGDPNRDAKVRDAVLMQAAPFDTPPVTLAQLGSRLAGISWGRGDLALLTESWWKTRKTKTWLIAPDNASAEPRLLWDRDAQDRYADPGRPLLASDERGRSLLQTSPDGSSLYLAGAGASPEGDRPFVDRFDIATGKATRLFHSQAPSYALPVALLDDQASSLLLSRESPDEPANFYVQSLADAGAAPRALTHFAHPLPQLKGVQKEQIRYKRKDGVDLTATLLLPPGYDPKRDGPRPLLMWAYPGEFKSAAAASQVTDSPYRFNAVSYWGPQAFLAKGYVVLASPSMPIIGEGDKEPNDTYIEQLVANAQAAVDEVVRRGVTDRDHIAIGGHSYGAFMTANLLAHTRLFKAGIARSGAYNRTLTPFGFQAEERNYWQAQDVYQKMAPFNYADRIKDPILFIHGVDDNNSGTFPIQSERMFAAVKGLGGTARLVMLPNESHAYRARESIMTMLAESERWLEQTIGPAEQGKAKKKR
>NZ_CP021768.1|WP_075675352.1|764444_765890_-|adenosylhomocysteinase
MNAVAKTFSTEGDYKIRDITLADWGRKELDIAEHEMPGLMSIRRKYQAELPLKGVRVTGSLHMTIQTAVLIETLKDIGADVRWASCNIFSTQDHAAAAIAATGTPVFAWKGETLEEYWDCTLDALTFTLADGTLTGPELVVDDGGDVTLLIHKGYELENGSDWVNTASSSHEEQVIKNLLKRVAKERPGYWGRVVKDWKGVSEETTTGVHRLYQLAQAGTLLIPAINVNDSVTKSKFDNLYGCRESLADGLKRAMDVMLAGKVAVVCGYGDVGKGCAASLRAYGARVIVTEIDPICALQAAMEGYEVNTIESTLGRADLYVTTTGNKDIIRIEHLSAMKDQAIVCNIGHFDNEIQVDALVSFAGVKHVNIKPQVDKYIFPNGNAIFLLAEGRLVNLGCATGHPSFVMSNSFANQTLAQIDLWANKDSYEKKVYLLPKKLDEEVARLHLEKIGVKLTTLSQEQADYIGVPVEGPFKPDHYRY
>NZ_CP021768.1|WP_087921550.1|763447_764233_-|hypothetical-protein
MPRNRDRMTRAMKPLMTLCWVALLAACSPPGSDAGATTTAASGQASTDGKAASTPAAAAGSSTACAEGASEVQTLICNDPALSQQEGELATAEASARDTLDAAGKDKLQAEQQRWIQHTRDLCGDAHCLQQVFADRLKVLSATRDGLVDQDACEVPDGQQQCVDLLVLRDPNSQLANFNTLLGENGQEGRLLGCTAATNMGGGPNAVLAANCIQETTAGKRNVQLCSNQMVGQFALEPAPAAYGTQAVRQLLGFTQQHCAG
>NZ_CP021768.1|WP_087924131.1|762053_763397_-|peptidoglycan-binding-protein
MATDSTLTREQLSTLFLNTELGGNTRHLDHFSYAQKGASTYSFGLVQFDVGGNPQARRFLRDNGFTAADIELLSQQGGLSTQQLAALDAKLQAIPQAKMDQLTNDKLDSAIGRVDEAIAKVRATNPAAADAIAANPELQLAMADYDNQFGSMGPQFINYLAGNAEKLQGGTVQAGNPPTRGDVQNFVDATKYGIQSPAAVTSRDERFDRAMTQLGITPTHAPSHGSPSAPGGNGVLVSGARGDEVQAMQQKLADLGYLGKDGKPLVADSDFGPGTLEAVKQFQREHQLTVDGKVGATTLGALDKAIAQQQQPATEPTMATPGHADNPRYQQVVEKLETLEEQRRQGGLSPLFKDRSQLENAAGQVAYESKLAGMSQVDTVLARPDNQGVFAVQGQLGDPAMHRTYVDLSQAVNHTLHDSTRQSQALDNELSQRQTQEQIQAQQSMSR
>NZ_CP021768.1|WP_087921556.1|777695_778523_-|class-I-SAM-dependent-methyltransferase
MTPPISSPTYLHGFSGTEQQRLMTQARLLESSIFGQIDYSGARRLLEVGSGVGAQTEILLRRFPELHVTGVDLSETQLATARENLARTPWCSDRYTLQQADASELPFEARSFDSAFLCWVLEHVPSPARVLSEVRRVLAPGSPVYITEVMNASFLLDPYSPHIWRYWMAFNDFQYDHGGDPFVGAKLGNLLLAGGFRDVHTEIKTIHLDNREPARRKTMIAFWEQLLLSAADQLLQAGSVDEDTVEGMRREFRLVQNDPNAVFFYSFVQGRATVY
>NZ_CP021768.1|WP_087924132.1|778639_779635_-|tRNA-dihydrouridine-synthase-DusB
MQIGPYTIAPNVVLAPMAGVTDKPFRLLCKRLGAGLAASEMTISDPRFWNTRKSIHRMDHEGEPAPISVQIAGTEPQQLAEAARYNVDHGAQIIDINMGCPAKKVCNAWAGSALMRDEQLVARILEAVVNAVDVPVTLKIRTGWDCDHRNGPVIARIAEASGIAALAVHGRTRDQHYTGQAEYGTIGEIKAALRIPVIANGDIDSPQKAAYVLKETGVDAVMIGRSAQGRPWIFREVAHYLATGEELPPPSLAEVRDILLGHLHALHAFYGEPQGVRIARKHLGWYAKDRPENAAFRAVVNRAEDPQSQIALTTEYFDRLIAGEPVLSSAA
>NZ_CP021768.1|WP_087921557.1|779782_780214_-|hypothetical-protein
MDGFPWLLVAAAGSAVAALLHIGCIAFGAPWYRYFGAGPRMVRLAQAGHWWPPLMTAGITAVLVTWTLYALAAAGWHSPLPGSRLVLPGIAALLLLRAAMGFGLALFRPGYNGVRFWAVSSLVCLALGLAFAAGTRQAWQGLG
>NZ_CP021768.1|WP_087921558.1|780363_781329_-|ribokinase
MSSSVVVVGSFNVDHVWRCESLPAPGATIAGRYSTGPGGKGFNQAVAACRAGADTHFVCALGDDAGGATARELAAQDGFALIAEASSEPTGTAGIYVDARGRNTIVIGPGANAALSTDFLQQQQALLTAAKVVLVQLESPVPTIEAALATAREAGVTTVLNTAPADAPSTIGLLKLADVITPNETEFAALLGRHVGERVEANDVAALDGASLHALCRKLVGNGTVVVTLGSVGVFVSHADENLRGDTQPYYRVGAEQVQAIDTTGAGDAFNGALAASLAQVADAPFARHVRFANQFAGRSTEKEGAAAAMPRFTPADAEAK
>NZ_CP021768.1|WP_014036013.1|781354_782653_-|nucleoside-transporter-NupC
MVEGLGRIGFGLFGLAVLIGITWLFSNNKRAVDWKLVATGITLQIAFAALVILVPGGRDVFDALGKGFVKVLSFVNEGSGFIFGSLMDTKNYGFIFAFQVLPTIIFFSALMGVMYHLNVMQAIVRVMAWSITKVMRVSGAETTSVCASVFIGQTEAPLTVRPYIARMTQSELLTMMIGGMAHIAGGVLAAYVGMLGGGDPAQQAFYAKHLLAASIMAAPATLVVAKLLIPETGTPLTRGTVKMEVEKTSSNIIDAAAAGAGDGLKLALNIGAMLLAFIALIALLNAPLTWIGDVTGLAAAIGKPTNLSTIFGYVLAPIAWVIGTPWADATTVGSLIGQKVVINEFVAYTELSQIVNGQVAGVSLSEEGRLIATYALCGFANFSSIAIQIGGIGGLAPERRHDLAKFGLRAVLGGTIATFMTATIAGVLTHFS
>NZ_CP021768.1|WP_087921559.1|782847_783819_+|aldo/keto-reductase
MQYRRLGSTGLPISALSFGAWVTFGDQIPRDEARNLVAAAWDHGVNFFDNAEGYANGRAEQVMGDVIADLRLPRDGICVSSKVFFGSAKDPRPTQRGLSRKHVTDACHAALKRLRVDYLDLYYCHRPDPDAPVAETVHAMDTLVRQGKILYWGTSEWSALQIQQALDIAAARNLQGPSMEQPQYNLLHRERVEVEYAPLYAGAGLGTTIFSPLASGLLSGKYDQGIPADARLGREGMEWLQALVLGDDAGARLAQVRRFSEVARALGHAPATLAIAWCLRNPNVSSVILGASRVSQLLQNLQALDVLERVDAAGWAQVEAVFA
>NZ_CP021768.1|WP_087924133.1|784035_784230_+|hemin-uptake-protein-HemP
MNAQPVLLRPETLTLRDRPVRVVAPEEVIDSEALLKGRREILIQHGDRFYRLRHTSNDKLILTK
>NZ_CP021768.1|WP_087921560.1|784422_786579_+|TonB-dependent-hemoglobin/transferrin/lactoferrin-family-receptor
MALPLSAHAAAAATAAPDAREFDRVQVTATRTDRAVSDVAATVDVIDREQMDRYLVQDIKDLLRYEPGLSVSRSAARFGLGSIRIRGLDGNRVRVQTDGIAMPTSFNIGSFSNANRNFTDLDTLKRVEIVRGPASSLYGSDALGGVVAFVTKDPADYLKDGKDSYVGLKFGYDGEWKGLLGGVTSAFGGEHWSGMVNINHRQGQETGNKGDVRSLDNTRTAPNPQDRDGRSGLAKLVYAPSEDQRFRLTVEGNEDNTDTNVLSSIDRTTTTGMKARDTQNRTRVSFAHEMDALDKGFADSLHWQLYTQHSETTQITDEDRANRSRRHREFNFDQRVYGLQAQFNKAFSTGSVEHALTYGFEGARTEIRQKRDGYQVLANGQTSTTILPDAFPVRDFPISKTTELGLYAQDEMRMANGKLSLVPGVRVDRYELKPEVDSIFAEDNPGVAVAKLTKTSVSPKLGMVYRFTDEWSLFAGYSHGFRSPPYNDVNLGFTNFAFGYTAIPNPDLKPETSDGMELGLRFLSPAAYVSLSGYYNEYKDFIESQSLVGTNAQGLMVFQSRNIADARIYGAEMKAGVDFGQISPALQGWALRSSAAWSRGDNKTEDTPLDSVDPLRGTVGLMYDTDTWGVELAGTFVKRKDRVTAATVYRPAGYGVADLMAHWNFAPGATFNVGVFNLGDKRYIDWSNVGSTLSPASRVLDRYTSPGRTLSASLAVSW
>NZ_CP021768.1|WP_087921561.1|786583_787183_+|Hemin-transport-protein
MSRALSARRNDAIAAQGSAAWPTPAQLATLGTVLCLYRADGNELGGWRQAVRVHACQGVDSEGVRESLCFLDVRGRCVWRLYLLPDSDFLAWDRLVAALPPGPEHDSDGSVGERLWRRLAGHLGGQRWRLCTLRLHAADDGRTLAASLSTLSSLGAATAHRIARLEGAEGELAIDDCCCADAARRPAPRIRGDLPLIRL
>NZ_CP021768.1|WP_087921562.1|787256_788192_+|hypothetical-protein
MKFQTASVMLLLAASGVASAQPSDIARDHDSILAMQGEYTVDFAFDETVLLKPGYERAPAMRSGGNELVIVVEDTPKRIVLQHLLLDEKSGHITKHWRQDWVYEAPSRFEFSADQTWQVRSIPATVNKGAWTQCVYEVSDAPRYCGTGTWTYTNNVPTWTSDLSWRPLPRREYTKRSDYNALAVVNRHTLTPNGWTHEQFNTKVQRNADGSQVEIAREFGFNDYVKTTEIDFTPARDYWKATAGYWAKVRQRWDGFLGQAPGVHLKTKLDGMAMIIPLFTQAEEIQSGKKVKDKQIDDVFAKYVEKAPKEG

Crispr_ID: NZ_CP021768_3

• CRISPR_ID: NZ_CP021768_3
• CRISPR_location: 1632528-1632833
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP021768_3

Consensus_repeat	Method
GCGGCGGCCCATGCGGCGGCCCGTGCGGCG	CRT

spacers of NZ_CP021768_3

>3.1|1632558|30|NZ_CP021768|CRT
GCCCATGCGGCGTCCCATGCGGCGTCCCGT
>3.2|1632618|30|NZ_CP021768|CRT
TCCCATGCGGCGTCCCATGCGGCGTCCCGT
>3.3|1632678|18|NZ_CP021768|CRT
TCCCATGCGGCGTCCCGT
>3.4|1632726|30|NZ_CP021768|CRT
GCCCGTGCGGCGGCCCGTGCGGCGGCCCGT
>3.5|1632786|18|NZ_CP021768|CRT
GCCCGTGCGGCGGCCCGT

CRISPR arrays and Neighbor proteins around NZ_CP021768_3

CRISPR arrays

The CRISPR arrays of NZ_CP021768_3

>merge|NZ_CP021768|3|1632528-1632833|CRT
GCGGCGTCCCATGCGGCGTCCCGTGCGGCGGCCCATGCGGCGTCCCATGCGGCGTCCCGTGCGGCGGCCCATGCGGCGGCCCGTGCGGCGTCCCATGCGGCGTCCCATGCGGCGTCCCGTGCGGCGGCCCATGCGGCGGCCCGTGCGGCGTCCCATGCGGCGTCCCGTGCGGCGGCCCATGCGGCGGCCCATGCGGCGGCCCGTGCGGCGGCCCGTGCGGCGGCCCGTGCGGCGGCCCATGCGGCGGCCCGTGCGGCGGCCCGTGCGGCGGCCCGTGCGGCGGCCCATGCGGCGGCCCGTGCGGCG

>NZ_CP021768|3|1|1632528-1632833|CRT
GCGGCGTCCCATGCGGCGTCCCGTGCGGCG	GCCCATGCGGCGTCCCATGCGGCGTCCCGT
GCGGCGGCCCATGCGGCGGCCCGTGCGGCG	TCCCATGCGGCGTCCCATGCGGCGTCCCGT
GCGGCGGCCCATGCGGCGGCCCGTGCGGCG	TCCCATGCGGCGTCCCGT
GCGGCGGCCCATGCGGCGGCCCATGCGGCG	GCCCGTGCGGCGGCCCGTGCGGCGGCCCGT
GCGGCGGCCCATGCGGCGGCCCGTGCGGCG	GCCCGTGCGGCGGCCCGT
GCGGCGGCCCATGCGGCGGCCCGTGCGGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_157721507.1|1629521_1630223_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922125.1|1631754_1632126_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922138.1|1638680_1639133_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922135.1|1636881_1638150_+|helicase-DnaB	unknown	unknown	gnl|CDD|273206
NZ_CP021768.1|WP_087922124.1|1631548_1631758_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922133.1|1636025_1636208_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922126.1|1632122_1632428_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922123.1|1631336_1631549_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922130.1|1634531_1635083_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|376540
NZ_CP021768.1|WP_087922117.1|1627509_1627881_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922120.1|1629117_1629522_-|single-stranded-DNA-binding-protein	unknown	unknown	gnl|CDD|223702
NZ_CP021768.1|WP_155761113.1|1635493_1635808_+|hypothetical-protein	unknown	unknown	gnl|CDD|238045
NZ_CP021768.1|WP_087922139.1|1639389_1639716_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922127.1|1633376_1633793_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922119.1|1628788_1629109_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922134.1|1636207_1636885_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922122.1|1630459_1630681_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922118.1|1627877_1628792_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922137.1|1638417_1638684_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922128.1|1633789_1634236_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_155761113.1|1635493_1635808_+|hypothetical-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	0.000121954
NZ_CP021768.1|WP_087922135.1|1636881_1638150_+|helicase-DnaB	gnl|CDD|273206	TIGR00665, DnaB, replicative DNA helicase. This model describes the helicase DnaB, a homohexameric protein required for DNA replication. The homohexamer can form a ring around a single strand of DNA near a replication fork. An intein of > 400 residues is found at a conserved location in DnaB of Synechocystis PCC6803, Rhodothermus marinus (both experimentally confirmed), and Mycobacterium tuberculosis. The intein removes itself by a self-splicing reaction. The seed alignment contains inteins so that the model built from the seed alignment will model a low cost at common intein insertion sites. [DNA metabolism, DNA replication, recombination, and repair].	1.07572e-108
NZ_CP021768.1|WP_087922130.1|1634531_1635083_-|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.	5.84908e-07
NZ_CP021768.1|WP_087922120.1|1629117_1629522_-|single-stranded-DNA-binding-protein	gnl|CDD|223702	COG0629, Ssb, Single-stranded DNA-binding protein [DNA replication, recombination, and repair].	3.73677e-19

Protein sequences

>NZ_CP021768.1|WP_087922126.1|1632122_1632428_-|hypothetical-protein
MSAPVDVLAAMVTLCSFGGGFEARRVVAEFNIPRSTSVIRSHLRPATTAQVRAALKKAERAGEVERVAVAPSWRECGAAADAELHWRITPNALARVKGGAA
>NZ_CP021768.1|WP_087922125.1|1631754_1632126_-|hypothetical-protein
MNADWHISRRDSEEDFRDPREVHIAERAAELLAEYQRDDEKIVEAVKEFMAYGDGEDHVRATWVFLCAYRNTETDRGIADAANALASDLQSYINPILREWAEDKAREEVAQNEASQSEVRSAA
>NZ_CP021768.1|WP_087922124.1|1631548_1631758_-|hypothetical-protein
MSTLTFPQDGDALRRLGNIRWLANTNHMDERAVVREFMEAGCSYEKQGELYERARRQRMNLGHGPKGAA
>NZ_CP021768.1|WP_087922123.1|1631336_1631549_-|hypothetical-protein
MKRGDSSAYPCKYSINGGIGLTKRELFAAMAMQGILGNSDPDICGWSNQEVARFAADQADALLDALENLK
>NZ_CP021768.1|WP_087922122.1|1630459_1630681_-|hypothetical-protein
MKAHYMVLASCIGLIVFLCWAAWFTYKYEAYYITACALLVALIDAFFIYDELHIIRKKRNDRFKQSPLTTERG
>NZ_CP021768.1|WP_157721507.1|1629521_1630223_-|hypothetical-protein
MADIPNLAGVATAELVEKIVGGSFQASYINWSRTLNLLREHAPGWLPESVPNHSGAILHEAPVGAYLLIRFRHVDGTVTPEVPQAVMDSRNAAIPMQKITARDITDTHRRGVCLAAALTFGLAYELWAKVALESGYQAEPEQADDQPTAEEIRRIKCEELCEANAESIEAIRDGLDSGDYVKAAEAWYELDQDTMRGLWVAPSKGGPFTTKQREIMKSAEFTKYRPTAEQEAA
>NZ_CP021768.1|WP_087922120.1|1629117_1629522_-|single-stranded-DNA-binding-protein
MNNFSAVGRIGRDAVTRFTQAGKAVTGWALAVDRGFGDNKQTVWLDCTLWGDRGQKLAEHIRKGDRLGVVGEIGTREHDGKTYVTLDVKDVTLLGGKQEGQSGGTSSRRGGQEQSERPQQQAPVSDFDDDSIPF
>NZ_CP021768.1|WP_087922119.1|1628788_1629109_-|hypothetical-protein
MSNEITRFNHVTDWGMERDSDGDYVLHSEHEAEVARLRAEVEWIRSWLPAMKVLVSAVEEEFCSELTEASEPDNSKVSYPEEDCPITFGMIREARKAIDAAMGASA
>NZ_CP021768.1|WP_087922118.1|1627877_1628792_-|hypothetical-protein
MTTDNKTLADVQPGGRVRLGDQRSDLVPGIVRCAKCQFQLARSNLNMHSGTVTAGDSKTEPCPNGCGPLWPVTWETWAREGWAEAERLHLENAALSAQPSPGGQGDAITPAMVDAAASVLARWAGHDDGSRWVHEARDALEAALAARQLVDDRFPGGFADAIAYVNQIEELAEGIHTQVFGHESDGETGATTVLQMVSYQLAEKPAQAIDARQPVGEPVAWMTHHDEPMLFPTAAEAAAYCEDDEQPVPLFRSPAQAVDLGQLQRFDHQLFENPWPYSGMEDAVEGNWVRFDDVKALIDKAVGK
>NZ_CP021768.1|WP_087922117.1|1627509_1627881_-|hypothetical-protein
MSWFSRWTKGQASLEDAITDAKVAISTHLHSLPVDVVEHVTEFRDGMRDRQNGTNGHYEMRRWLQRLKDLRARLAHLERAEVMRSQIAAHLGMKPDKVDMDELLRLLREADAHGESEPEPTHG
>NZ_CP021768.1|WP_087922127.1|1633376_1633793_-|hypothetical-protein
MKLIALALLSAASANAADGIQAVPSDELCIAMAVGMITGSQEVKDSVRPELERRSETCAPADMYIKIAEARIGFMQAKAATPQPPAPEPKPSMRQRIGQAADAYLELQRQQQLQRQTRPVPTTTTCNSFEGMTTCHTW
>NZ_CP021768.1|WP_087922128.1|1633789_1634236_-|hypothetical-protein
MMRLSLFAIAVLASATAQAGNWKPDSASGFRAASTMDKHGNQFGVTCKESGGACVWVIKTKKECRAAGQFDIKIITDGVPIPSKVQCFPREGEDPAFFAISNFDQVMQLIPLSKTLAFESDAQPLVSSGPFQVEDTDGVLARLAEDTK
>NZ_CP021768.1|WP_087922130.1|1634531_1635083_-|helix-turn-helix-transcriptional-regulator
MEPWAERIEAVLREGRARGLTKTGLAKACGKAQPSISQWFNDNESKPATQMIMADNLIAAARYLGVTPEWIMTGSDWFNRDAEASQPVRMDVSKIAETAKILRTVFERRGVAFDPVEDADVFAEVYALLDQMPVNPSQEANVAFTATVIDLVAKRLERGDGRGSGKQDRGSAGKQVVRKVGVA
>NZ_CP021768.1|WP_155761113.1|1635493_1635808_+|hypothetical-protein
MADEKTVRMCESEEDAIAVGIVLSGLTQAEIAARMGISKVYLTLMKQGQRTMTVKMLSRFCSATGWNVVRQYRDLQMALRVATGTPREVDRIAQIASHTMRKVA
>NZ_CP021768.1|WP_087922133.1|1636025_1636208_+|hypothetical-protein
MKHIARAMDGLPIPDIEELLAAPPLTEVELAQFNSLRAAEMARAEKRRMPSPQLDLGEVA
>NZ_CP021768.1|WP_087922134.1|1636207_1636885_+|hypothetical-protein
MARIRTIKPEFFTSEDICALSPMARLLYVALWCEADREGRLTWKPRTFKLRYFPADDCDIDALARELVASGLVIPYGDGFAFIPKFAAHQHINPRETASSLPEPDASERVSDASLRVSDTQGGREGKGREGKEHASGDATRKRAPSKSVLPADFGISARVRSWASEKGHDRLEQHLESFRAKATAKGYTYADWDAAFMEAIRENWAKLPTKVVQLHQAGGGRREL
>NZ_CP021768.1|WP_087922135.1|1636881_1638150_+|helicase-DnaB
MSDVTPAFAEEAVLGGLLLENLRFHDIAPLIGADHFTSRQRSELFGLIRDRVLAGEDADAVTIGELSPDHFDMALSLAANVPSASSVVLYARIVRENWRRREAVQAGLQLVSSAKAGEEDAVDVAVAKLLSLNATVADCEFTGKQAMQQAWKEVVRTHENGGNLPGITTGLKALDEILGGWHDSDLTVVGGRPAMGKTAFLGGLVEAAASVGKRPGVISAEQPAVQLALRRLSMVSSVSASSLRSGQFNDEDWGLMQAGMAKALPRDMWIYDRSAVTLDELIGVARKWKHANDIGILFIDYAQRIRVPRADRITEVSLVAQGMKDLARSLNIPVVSLAQVVKGVETRNDKRPNAGDLANSDELTREADQILMLYRDEVYNRDSPDKGVAEVLIEKNRHGPTGFKKVAFLSETMRFADLGRDF
>NZ_CP021768.1|WP_087922137.1|1638417_1638684_+|hypothetical-protein
MSKFFVGQRVRIKLSGEFPHLAGTEARIIGDGIVGSDPVWEISAAGEDDWYVEKYQAPFVLDPILPEGSAPSEFTFQQLMDNLQEVMA
>NZ_CP021768.1|WP_087922138.1|1638680_1639133_+|hypothetical-protein
MKLIINSETALQSAVGQLREQFKERKYLTVSITHGKARSLDQNAISHAWYEQVARELREDTPLGVKAFCKLTMGVPILRAEDDEFRAKYDKAVKPMAYEDKLILMEWFPVTSLMTTPQLSQYLESVQRHYQRLGVWLEFPEPQNKQRVAA
>NZ_CP021768.1|WP_087922139.1|1639389_1639716_+|hypothetical-protein
MNLEQIDTSTTAGKAEVMRLAAEGRRVALRGIWSTEPFYEMGDGYEICWNWESTIYAIISEPVGPEEVWLVIDHSMDALTEASAKSYAEAHGLQVVRYRRADLAGEKQ

Crispr_ID: NZ_CP021768_4

• CRISPR_ID: NZ_CP021768_4
• CRISPR_location: 2397180-2397256
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_4

Consensus_repeat	Method
TGGTGGGTGCCGACCTTGGTCGGCA	CRISPRCasFinder

spacers of NZ_CP021768_4

>4.1|2397205|27|NZ_CP021768|CRISPRCasFinder
TCTACCAACAGCCTCCATGTATCGTTC

CRISPR arrays and Neighbor proteins around NZ_CP021768_4

CRISPR arrays

The CRISPR arrays of NZ_CP021768_4

>merge|NZ_CP021768|4|2397180-2397256|CRISPRCasFinder
TGGTGGGTGCCGACCTTGGTCGGCATCTACCAACAGCCTCCATGTATCGTTCTGGTAGGTGCCGACCTTGGTCGGCA

>NZ_CP021768|4|3|2397180-2397256|CRISPRCasFinder
TGGTGGGTGCCGACCTTGGTCGGCA	TCTACCAACAGCCTCCATGTATCGTTC
TGGTAGGTGCCGACCTTGGTCGGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087922678.1|2387462_2389658_+|TonB-dependent-siderophore-receptor	unknown	unknown	gnl|CDD|273805
NZ_CP021768.1|WP_087922691.1|2401776_2402622_+|DUF4974-domain-containing-protein	unknown	unknown	gnl|CDD|226235
NZ_CP021768.1|WP_087922688.1|2399602_2400775_-|low-temperature-requirement-protein-A	unknown	unknown	gnl|CDD|377704
NZ_CP021768.1|WP_087922680.1|2390622_2391288_-|conjugal-transfer-protein	unknown	unknown	gnl|CDD|237542
NZ_CP021768.1|WP_087922683.1|2393590_2396350_+|magnesium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|236705
NZ_CP021768.1|WP_087922689.1|2400784_2401051_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922679.1|2389802_2390159_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922681.1|2391402_2392350_+|prolyl-aminopeptidase	unknown	unknown	gnl|CDD|130316
NZ_CP021768.1|WP_087922677.1|2386630_2387224_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP021768.1|WP_087922694.1|2406230_2406770_-|DUF411-domain-containing-protein	unknown	unknown	gnl|CDD|225564
NZ_CP021768.1|WP_087922687.1|2399048_2399594_+|DUF1697-domain-containing-protein	unknown	unknown	gnl|CDD|377954
NZ_CP021768.1|WP_087922686.1|2398410_2399052_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|226932
NZ_CP021768.1|WP_087922693.1|2405215_2406088_+|L1-family-subclass-B3-metallo-beta-lactamase	unknown	unknown	gnl|CDD|293847
NZ_CP021768.1|WP_049445012.1|2392634_2392934_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922685.1|2397362_2398418_+|two-component-sensor-histidine-kinase	unknown	unknown	gnl|CDD|226654
NZ_CP021768.1|WP_087922692.1|2402693_2405120_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP021768.1|WP_087922682.1|2393227_2393527_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922690.1|2401255_2401780_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP021768.1|WP_087922684.1|2396377_2397115_+|MgtC/SapB-family-protein	unknown	unknown	gnl|CDD|224204
NZ_CP021768.1|WP_087924180.1|2385472_2386561_-|winged-helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225755

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087922678.1|2387462_2389658_+|TonB-dependent-siderophore-receptor	gnl|CDD|273805	TIGR01783, Ferrienterobactin_receptor, TonB-dependent siderophore receptor. This subfamily model encompasses a wide variety of TonB-dependent outer membrane siderophore receptors. It has no overlap with TonB receptors known to transport other substances, but is likely incomplete due to lack of characterizations. It is likely that genuine siderophore receptors will be identified which score below the noise cutoff to this model at which point the model should be updated. [Transport and binding proteins, Cations and iron carrying compounds, Transport and binding proteins, Porins].	3.84087e-106
NZ_CP021768.1|WP_087922691.1|2401776_2402622_+|DUF4974-domain-containing-protein	gnl|CDD|226235	COG3712, FecR, periplasmic ferric-dicitrate binding protein FecR, regulates iron transport through sigma-19 [Inorganic ion transport and metabolism, Signal transduction mechanisms].	1.19039e-52
NZ_CP021768.1|WP_087922688.1|2399602_2400775_-|low-temperature-requirement-protein-A	gnl|CDD|377704	pfam06772, LtrA, Bacterial low temperature requirement A protein (LtrA). This family consists of several bacteria specific low temperature requirement A (LtrA) protein sequences which have been found to be essential for growth at low temperatures in Listeria monocytogenes.	3.62783e-98
NZ_CP021768.1|WP_087922680.1|2390622_2391288_-|conjugal-transfer-protein	gnl|CDD|237542	PRK13882, PRK13882, conjugal transfer protein TrbP; Provisional.	3.44871e-78
NZ_CP021768.1|WP_087922683.1|2393590_2396350_+|magnesium-translocating-P-type-ATPase	gnl|CDD|236705	PRK10517, PRK10517, magnesium-transporting P-type ATPase MgtA.	0
NZ_CP021768.1|WP_087922692.1|2402693_2405120_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	1.44908e-53
NZ_CP021768.1|WP_087922681.1|2391402_2392350_+|prolyl-aminopeptidase	gnl|CDD|130316	TIGR01249, Putative_proline_iminopeptidase, proline iminopeptidase, Neisseria-type subfamily. This model represents one of two related families of proline iminopeptidase in the alpha/beta fold hydrolase family. The fine specificities of the various members, including both the range of short peptides from which proline can be removed and whether other amino acids such as alanine can be also removed, may vary among members.	1.04043e-134
NZ_CP021768.1|WP_087922677.1|2386630_2387224_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	0.000179579
NZ_CP021768.1|WP_087922694.1|2406230_2406770_-|DUF411-domain-containing-protein	gnl|CDD|225564	COG3019, COG3019, Predicted metal-binding protein [General function prediction only].	5.54859e-48
NZ_CP021768.1|WP_087922687.1|2399048_2399594_+|DUF1697-domain-containing-protein	gnl|CDD|377954	pfam08002, DUF1697, Protein of unknown function (DUF1697). This family contains many hypothetical bacterial proteins.	1.78105e-42
NZ_CP021768.1|WP_087922686.1|2398410_2399052_+|response-regulator-transcription-factor	gnl|CDD|226932	COG4566, TtrR, Response regulator [Signal transduction mechanisms].	2.70726e-85
NZ_CP021768.1|WP_087922693.1|2405215_2406088_+|L1-family-subclass-B3-metallo-beta-lactamase	gnl|CDD|293847	cd16289, L1_POM-1-like_MBL-B3, Stenotrophomonas maltophilia L1, Pseudomonas otitidis POM-1 and related metallo-beta-lactamases, subclass B3; MBL-fold metallo-hydrolase domain. MBLs (class B of the Ambler beta-lactamase classification) are a diverse group of metallo-enzymes that are capable of catalyzing the hydrolysis of a wide range of beta-lactam antibiotics. MBLs have been divided into three subclasses B1, B2 and B3, based on sequence/structural relationships and substrates, with the B1 and B2 MBLs being most closely related to each other. This subgroup of L1- and Pom-1-like MBLs belongs to the B3 subclass. Subclass B3 enzymes are most active with two zinc ions bound in the active site, and have a broad-spectrum substrate profile. These B3 enzymes have a modified Zn2/DCH site (Asp-His-His).	4.11704e-153
NZ_CP021768.1|WP_087924180.1|2385472_2386561_-|winged-helix-turn-helix-domain-containing-protein	gnl|CDD|225755	COG3214, COG3214, Uncharacterized protein conserved in bacteria [Function unknown].	3.90442e-59
NZ_CP021768.1|WP_087922690.1|2401255_2401780_+|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	6.61806e-24
NZ_CP021768.1|WP_087922684.1|2396377_2397115_+|MgtC/SapB-family-protein	gnl|CDD|224204	COG1285, SapB, Uncharacterized membrane protein [Function unknown].	1.20131e-56
NZ_CP021768.1|WP_087922685.1|2397362_2398418_+|two-component-sensor-histidine-kinase	gnl|CDD|226654	COG4191, COG4191, Signal transduction histidine kinase regulating C4-dicarboxylate transport system [Signal transduction mechanisms].	1.8044e-44

Protein sequences

>NZ_CP021768.1|WP_087922684.1|2396377_2397115_+|MgtC/SapB-family-protein
MDINPNLPAFNAGATLSSLISLSVAFVLGAAIGLERQLRQRTAGLRTNTLVAVGAAVFVDLAVRFHDLYGGPPSPLHVVAYVISGVGFLGAGAIMKDGAQVSGLNTAATLWGSAAVGACAGIKLLPEAVMAAVFVLAANTLLRPVVNRIQRQPLPEAFSEATYAINVVCQREQQAEVLDQLLLLLEQAHYPVRAVDQRPFGERDVEIEAVLYATTVDAGELDAVLATLATTPGVLQGFWNASLEE
>NZ_CP021768.1|WP_087922683.1|2393590_2396350_+|magnesium-translocating-P-type-ATPase
MSLLNAWFNAFLRSRRAGNLFRRRAMPEAGSGPGSAEAAPFALTTGLVTLAQQDEAELLATLESHADGLSPHEAEERLATLGPNEVDHEKPLPWWRHLWQCYRNPFNLLLTVLAAVSWLTEDIKATIVIGAMVLLSTLIRFVQEGRSNRAAERLKALVGNTARVLRRNPGTEAADVADQYFGAHLHSRRPARLLDLPIRKLVPGDHVVLSAGDMIPADCRVLNAKDLFVAQAAMTGESLPVEKFAHPGDGLAGLLEQHNLLFMGTNVVSGTATAVVLATGNRTYFGTLAQRSTATDRAPTAFQAGVNSVSWLLIRFALVMVPFVLLINGWTKGDWTEAFLFALSVAVGLTPEMLPMIVTSTLAKGAVLLSRRKVIVKRLDAIQNFGAMEVLCTDKTGTLTQDKIALERHTDVFGHDSEDVLKFAYLNSHFQTGLINLLDRAVLEHVELQSSLRLSQDYHKVDEIPFDFERRRMSVVVSEREDHHELICKGAVEEMLAVCGTVRENGEDKPLDEQRLARVRQTTEELNEQGLRVVAVAMKETTASQTVYSQADECGLTLVGYVAFLDPPKESAAQALQALAAHGVEVKVFTGDNELVTARVCAQVGLDADTILTGPQIERMDDGALSRALHHHRVFARLTPLHKERLVRELRAQGKVVGFLGDGINDAPALRAADIGISVDSAVDIAKEAADIILLEKNLMVLEEGVIQGRRTFNNMLKYIRMTASSNFGNVFSVLVASAFLPFLPMLPLQLLVQNLLYDISQIAIPFDNVDEELVRKPLKWNPADIGRFMVFFGPISSIFDLSCFALMWYVFDARTPADQGLFQSGWFVVGLLTQTLIVHMIRTPKVPFLQSIAAPPLLVMTGLIMAIGVALPMSPLAGYFKLQALPTGYWPFLVAILFGYAVLTTALKKFYIRRYGWQ
>NZ_CP021768.1|WP_087922682.1|2393227_2393527_+|hypothetical-protein
MSYKILYITLRRLIGERDVAALRSQLLQRGPVMFARSLSLGSPRVVADALSLLPISERINVLRHLPYPLRDAMKPLCIGGSQRLHMQPWSPAVLAMRHA
>NZ_CP021768.1|WP_049445012.1|2392634_2392934_+|hypothetical-protein
MTGVRYLPVALALCAGLLLGGCSKTQEASKATAAEDVTEVKLIPAYESLDKDKDGIVTLAEVDAVAPDWAERLHACDTDRDQKLTRGEYDVCKQTSTAH
>NZ_CP021768.1|WP_087922681.1|2391402_2392350_+|prolyl-aminopeptidase
MRTLYPAIEPYREFTLPVSDLHTLHIEECGTPEGIPVVYLHGGPGAGISPTHRRFFDPARYRIVLIDQRGSGRSTPFGELRDNTTQDLVADIEKVREHLGIERWLVYGGSWGSTLSLAYAQAHPERATGLIVRGVFLGREMENRWFAEANGGARWIFPERWDRYEAYIPEAERGDMVAAYWKRLNSADEATCIEAAQAWLGWEDNAATLQHDVDAQSSDDPLDTLAKARIEAHYFRNGIFLEPDQLLRDIDRIRHLPGVIVQGRYDIICPPRSAWDLAKAWPEAKLEMVTSGHSANEPATVDALVRATDAFADRF
>NZ_CP021768.1|WP_087922680.1|2390622_2391288_-|conjugal-transfer-protein
MQATTTGTSTPDPILGSGARELLKWIALLTMTGDHVAKVVFGGYLPVVSELGRIAFPLFALVMACNLAQPGADPRKSIRRLALWGLIAQPLHALAFGSWLPLNILLTFALAAVAVHALANNRPVQLLLAAGLLPMLVDYQWAGVGSVLLAWIAFRHRAWWLLLAALAAVCWANHNGWALLAIPIVLLAARVPWQLPRWRWTFYGYYVGHLAVLALIAHLLA
>NZ_CP021768.1|WP_087922679.1|2389802_2390159_-|hypothetical-protein
MNASEFPHQHAPANADEGHDVPPDLNSLTALLHRIGLGAAADGQPWPERHQLPGRCLALADADGALAGLRIVNEILLAAERARQNGGPDQYVGDRVMEGLKLAALALTNQAIYRLHPE
>NZ_CP021768.1|WP_087922678.1|2387462_2389658_+|TonB-dependent-siderophore-receptor
MTVYPLSSPLQPAAAAASRMQMHPPMARRYRVSALALGLLASFAALADSAPSTLPSVQVQEQRRVTGDYAGGQVASGSRVGLLGDKDFMDTPFSTVSYTEAFIRDRQAKDLTDVIAATDPTVFSNGVTGAWSENYAIRGFASSTSDTTFNGLSGMAPYYRTSPEMFERIEVLKGPSALLNGMPPGGSVGGSVNLVPKRAGDQPLLRVSANFVSDAQFGTHVDVGRRLGADKQFGIRFNGAYRDGDGAVGKQSKKVQLGSLALDWRGERARLSADLYSADDRVDGPARGVGLAPGVAIPRPPRGDTLINPDWAYVDSQDKGAMLRGELDINEHLMTYLAYGTSKTDYRYNGSISAQILNPAGDFTTVMGQLAFDIRKQSGDAGLRGSFRTGSVSHQWAANVTHYQHTQNDYGRRSVPGWDWTTNLYNPVWGPAAPFVAPHISHTELRLDSLGFADTLSFADDRVQLTLGVRRQQVVSETFNVASGARTSRYDESATTPAAALLVKATDTISVYTNYIEGLSQGATAPMTAANAGDVFAPFRTKQKELGLKLDLGSFAHTFSVYEIKRPSSYTDPVTNIFSFGGEQRNRGVEWGFFGSPLDGVRLLGGVAYVQPKLTRTAGGVNEGRIATAVAQRQAKLGVEWDVPAFQGLTLTGNATAMSKQYISADNRLSVPGRTLFDVGARYSTTMAGRPLALRASVNNVTNKAYWGMPLLSSLALGAPRTVLVSATMDF
>NZ_CP021768.1|WP_087922677.1|2386630_2387224_-|TetR/AcrR-family-transcriptional-regulator
MNMHPETPASARGRPPTITPDRLADIGIKLGLPNLTMANVAAELAVTHAALYKRVANLEALKRLVADRVFQRWQIPRASPDAPGGLQAYLLGFVESLCEVVKAHPGLPPYLLRRSVATTPMLEKIASHQAHVAEVFGLPLDKARWLLATIAFYCIAGADTVYGIADDEEGQVITEFKQGMRALVIGSLEVLNEDGNS
>NZ_CP021768.1|WP_087924180.1|2385472_2386561_-|winged-helix-turn-helix-domain-containing-protein
MPATPTLDDLRRHAVARTLFKPTTLLAAIRRLGFVQADPIRAPARAQDLTLRHRVKDYRAGDLERRYTRLPVEEDCLVNYGFLPREHLALMHPRVSKRAWDAETQRRAADVLAFVRERGSVHPREVDQAFAHGRVTNYWGGTSNASTHLLDGMHYRGLLRVQRRDSGTRIYAVAEHAEADASEQAQIERAAALIDLVVRKYAPLPSASLTYLVRLLGYGAPHLAEQTRQALKLAKQQLASCTLDGTTWYWPADENPRSRRHAPDDQVRLLAPFDPVVWDRRRFELLWGWVYKFEAYTPAPKRQYGYYALPVLWHDQVVGWANLIVRDSELVSGVGYAGKSLARDKVFRGALDDELQRMAAFL
>NZ_CP021768.1|WP_087922685.1|2397362_2398418_+|two-component-sensor-histidine-kinase
MPSLSPRRPLVLLVLIVVMAAIFLIDTVTDYAVAAACFYAAVILAASRVLSARGLITLAIACIVLTGLSFFLTRFGTYRIGLVNSVIGMLVIGITTYLALNMEAAKAAVQEAQARLLRVARASTVGELTTSIAHEVNQPLAAIASSAEACQRWLAQDPPNVDKARQTVARILADAHRAGDVIARIRGLTQGAAPERRAFDLNQAVEEMLALSRSELDQHDVAVALLLDADLPLVQADRVQVQQVIGNLILNAVDAMEAVPAADRRLSLLTRRDGQRVSLSVRDRGVGLPADHPERVFDAFWTTKSHGLGLGLSLSRSMIEANDGQIRAERPAGGGACFVFDLPIATDSPHA
>NZ_CP021768.1|WP_087922686.1|2398410_2399052_+|response-regulator-transcription-factor
MRKPAAPIADPAPIVYVIDDDPSVRAALEDLLASMGLQVRAFASTQAFLEHELEDAPACLVLDVRMPGQSGLEFHRTMRSHGLQLPVVFITGHGDIAMGVNAIKDGAIEFLTKPFRDQELLDAIHKGIEIDRQRRRDGEALDALQQRWNTLNAGEREVVDGVVRGRLNKQIAGDLGVSEITVKVRRAQVMRKMGARTLVDLVRMYDRLQAGTP
>NZ_CP021768.1|WP_087922687.1|2399048_2399594_+|DUF1697-domain-containing-protein
MSVHVALLRAVNVGGTGKLPMVELVAMCEEAGFTDVRTYIASGNVVFRSGLGEAGVRKALGQRLQAYAGKPVGVLVRSAAEIAAVAAGNPFPHAAGNRVVALFVDGVLPTDPLTGVTGLRDEQLALGTREIFVHYGDGMADSRLRIPYAQQGTARNLNTVGKLAAMAAALGQVNADGGGRR
>NZ_CP021768.1|WP_087922688.1|2399602_2400775_-|low-temperature-requirement-protein-A
MSTRLRLPALRHRDGHHARVTYEELFFDLVYVFAVTQLSHHLLHHLDLAGVLQTLVLWFAVWLGWQYACWVSNWFDPQAPRIRGLLFATMLLALLMSSSIPEAFADRAWMFAGAYATMQVGRTAFVLLEVGRNHPLAPNFRRMLAWVSVAACFWLAGAAAEGNLRLALWAVAVACEYISPMFGFAFPGMGRSHTRDWTIEGGHLAERCQLFVIVALGETLLATGGVLSEVGHWSLQVVSAVLATFAGTIAMWWLYFGISSRDATEAITHADDPGRMGANFHYVHALLIAGIIATAVGNDLVMDHPHSAVTPVYAAVLVAGPLIYLLGSSLYKRVVYGRAPHSHLIGAVALGVLGFVLPHAHLLAAGWLTSAVLLAVGLMDTRLKHRLQRR
>NZ_CP021768.1|WP_087922689.1|2400784_2401051_-|hypothetical-protein
MHVILVITAGVLLLGVFLLFGHLWSVATSQLPTALIAFIATWLLVAVANMWVGVSRAGYAVREELPILLLVFAVPALLAGFLYWRLAR
>NZ_CP021768.1|WP_087922690.1|2401255_2401780_+|RNA-polymerase-sigma-factor
MSQLPSPHTPALPLVSSLVRHYEELVDYLRRRFHSPGLAREVVHDVCVRLLERPPAHDARQPIALLRRIAHDAAVDRCRAEDLRRHWVEPRAELPEGACPRPGPEQQAQGMHALEYLSITIERMPCRRQQVFILHKIHELPQAEVAQRMGIGLKAVERHLRLAMADCRLQAGLQ
>NZ_CP021768.1|WP_087922691.1|2401776_2402622_+|DUF4974-domain-containing-protein
MSRTPAPSEPPPPPTSTKQVLEQHRDALKQRFPLPSPEALQRRRSAGPTKAALALLLVAAGTLLAADPAWQVRDYQTAVGERRNVTLPDGSEVLLDAGTRLQVRRHLRSRQVLLVRGQARFEVQHSAWRRFQVDAGPVHVRNYGTVFDVDRQGDLSEVTLWRGEVGVRVDGSEAEQRLKPGQRLLAQAGSLSPPEAVSPDRADWTHGRLQFDRLPLSEVLRILQRYHDRPIVLDDPALGPLLVSGVFDADRAETAVALLPDILPVQLQTAADGSLHLRARD
>NZ_CP021768.1|WP_087922692.1|2402693_2405120_+|TonB-dependent-receptor
MTRPVPPAALRRLAPTLLAACLCAALPAAAQASAPAAVEFHLPAGSLQASLNALARQSGIQLLFAAESVGGRSAPALDGRYTPREALQRLLAGQGLALQERSPGVFVLSAAATAPAPAKATAPAPPAPQAAATSLARVTVSASTARMPQGETAMPNTITVLTREDIAQQLALGSDVSRVLSSQIPAFAPAREKMSNYGETMRGRGILYMVDGVPQSTPLRDGSRDSHTIDAAMIERIEVIHGANALQGIGGTGGIVNIITRSAPSEPEAFLFDSNLSYSAALPRRHDDNGQRASALVGMRGEQFDLVAGLAYERQGLFHDGEGRSIGTNAQGELMDSTSSNVFAKLGWNIAEGQRLQLMASRYELRGLDNYLAVNGDYRSGRPTLSVPGDTPLDPPMNRSRSLTLDYSAADLLGGRFQAQAFAVDFEGRYGASQWDPWGNTGANAAWDQTQNESDKRGFKLTQNWSRIAGTTLDVTLGLDGLRDRTHQVLLASGMNWVPLTTYQSLSPLLQLHWWPTDHLMLSGGLRYEKGELEVGDYTTLPRYGARKVAGGKPTMSETLPNFGAVWYINDRLNAYASYSEGYTVADVGRVLRAINRDGQRVDSLVDLSPVVSDNREIGLEYDDGRFSGDIAYYTSESKLGSVLVYDAGIDAYNVQRQATRVEGFETNLRLRLGNSRLGLGYARANGRYDANIDGRLDSDLAGVNIAPNRLTAFWEQNWTPQLSTRLQASHAFDRDFDLHGARVAEFKGYTTVDLVARYTLDKHAFTLGVQNLSNTQYISYYSQTTPSNPGYFSGRGRVLTLGWQYRY
>NZ_CP021768.1|WP_087922693.1|2405215_2406088_+|L1-family-subclass-B3-metallo-beta-lactamase
MRCSLLAFALAAALPAAHASAAEAPLPQLRAYTVDASWLQPMAPLQIADHTWQIGTQDLTALLVQTADGAVLLDGGMPQMASHLISNMKVRGVAPEDLRLILLSHAHADHAGPVAELKRRTGAKVAANAESAVLLARGGSNDLHFGDDITYPPANADRIIMDGEVVTVGGIAFTAHFMPGHTPGSTAWTWTDTRDGKPVRIAYADSLSAPGYQLQGNARYPRLIEDYRNSFTTVRNLPCDVLLTPHPGASNWNYAAGSKASANVLSCKAYADAAEKKFDAQLAKEVAGAR
>NZ_CP021768.1|WP_087922694.1|2406230_2406770_-|DUF411-domain-containing-protein
MNRSLSLGLLLGTVLASTACARAAEESPAAPVASQAPAAPIKASPSQVDPALPIAIVHKTASCGCCGIWVDHLKAEGFQVDVRDTDDMNPIKVRLGVPVGKASCHTAEIGGYVVEGHIPAEDIKRLLAERPAARGLVLPGMPAGSPGMEMPDGYVQPYTVELVRNDGTTEPFAQHGQGS

Crispr_ID: NZ_CP021768_5

• CRISPR_ID: NZ_CP021768_5
• CRISPR_location: 2419465-2419566
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_5

Consensus_repeat	Method
CGGTAGCGCCGGCCGCTGGCCGGC	CRISPRCasFinder

spacers of NZ_CP021768_5

>5.1|2419489|54|NZ_CP021768|CRISPRCasFinder
GGGAAGCCCCCATCCACGCATGGCGTGGATCTACTGAAACATTCACGCAGCCAA

CRISPR arrays and Neighbor proteins around NZ_CP021768_5

CRISPR arrays

The CRISPR arrays of NZ_CP021768_5

>merge|NZ_CP021768|5|2419465-2419566|CRISPRCasFinder
CGGTAGCGCCGGCCGCTGGCCGGCGGGAAGCCCCCATCCACGCATGGCGTGGATCTACTGAAACATTCACGCAGCCAACGGTAGTGCCGGCCGCTGGCCGGC

>NZ_CP021768|5|4|2419465-2419566|CRISPRCasFinder
CGGTAGCGCCGGCCGCTGGCCGGC	GGGAAGCCCCCATCCACGCATGGCGTGGATCTACTGAAACATTCACGCAGCCAA
CGGTAGTGCCGGCCGCTGGCCGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087922711.1|2422891_2423590_+|heavy-metal-response-regulator-transcription-factor	unknown	unknown	gnl|CDD|130454
NZ_CP021768.1|WP_087922710.1|2421961_2422846_+|copper-homeostasis-membrane-protein-CopD	unknown	unknown	gnl|CDD|224195
NZ_CP021768.1|WP_087922702.1|2415935_2416487_-|DUF3299-domain-containing-protein	unknown	unknown	gnl|CDD|378700
NZ_CP021768.1|WP_087922708.1|2420643_2421447_+|2,5-didehydrogluconate-reductase-DkgB	unknown	unknown	gnl|CDD|183012
NZ_CP021768.1|WP_087922713.1|2424934_2425846_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176161
NZ_CP021768.1|WP_087922709.1|2421573_2421951_+|copper-homeostasis-periplasmic-binding-protein-CopC	unknown	unknown	gnl|CDD|377255
NZ_CP021768.1|WP_087922705.1|2418427_2418961_-|DUF2796-domain-containing-protein	unknown	unknown	gnl|CDD|378529
NZ_CP021768.1|WP_049396107.1|2410665_2411202_-|peroxidase-related-enzyme	unknown	unknown	gnl|CDD|130981
NZ_CP021768.1|WP_087922715.1|2426796_2429874_-|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl|CDD|226220
NZ_CP021768.1|WP_087922703.1|2416489_2417743_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223650
NZ_CP021768.1|WP_087922697.1|2411308_2412190_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|378976
NZ_CP021768.1|WP_087922716.1|2429870_2431043_-|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776
NZ_CP021768.1|WP_087922714.1|2425952_2426696_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187620
NZ_CP021768.1|WP_087922700.1|2414567_2415314_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922707.1|2419622_2420525_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176167
NZ_CP021768.1|WP_087922701.1|2415313_2415946_-|DUF3299-domain-containing-protein	unknown	unknown	gnl|CDD|378700
NZ_CP021768.1|WP_087922699.1|2412854_2414387_-|MFS-transporter	unknown	unknown	gnl|CDD|184957
NZ_CP021768.1|WP_087922698.1|2412292_2412850_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_CP021768.1|WP_087922712.1|2423586_2424954_+|heavy-metal-sensor-histidine-kinase	unknown	unknown	gnl|CDD|273593
NZ_CP021768.1|WP_087922704.1|2417735_2418431_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213222

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087922711.1|2422891_2423590_+|heavy-metal-response-regulator-transcription-factor	gnl|CDD|130454	TIGR01387, Transcriptional_regulatory_protein_PcoR, heavy metal response regulator. Members of this family contain a response regulator receiver domain (pfam00072) and an associated transcriptional regulatory region (pfam00486). This group is separated phylogenetically from related proteins with similar architecture and contains a number of proteins associated with heavy metal resistance efflux systems for copper, silver, cadmium, and/or zinc. Most members encoded by genes adjacent to genes for encoding a member of the heavy metal sensor histidine kinase family (TIGRFAMs:TIGR01386), its partner in the two-component response regulator system. [Regulatory functions, DNA interactions].	7.91337e-114
NZ_CP021768.1|WP_087922710.1|2421961_2422846_+|copper-homeostasis-membrane-protein-CopD	gnl|CDD|224195	COG1276, PcoD, Putative copper export protein [Inorganic ion transport and metabolism].	1.15472e-20
NZ_CP021768.1|WP_087922702.1|2415935_2416487_-|DUF3299-domain-containing-protein	gnl|CDD|378700	pfam11736, DUF3299, Protein of unknown function (DUF3299). This is a family of bacterial proteins of unknown function.	2.98891e-47
NZ_CP021768.1|WP_087922708.1|2420643_2421447_+|2,5-didehydrogluconate-reductase-DkgB	gnl|CDD|183012	PRK11172, dkgB, 2,5-didehydrogluconate reductase DkgB.	0
NZ_CP021768.1|WP_087922713.1|2424934_2425846_-|LysR-family-transcriptional-regulator	gnl|CDD|176161	cd08472, PBP2_CrgA_like_3, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator CrgA-like, contains the type 2 periplasmic binding fold. This CD represents the substrate binding domain of an uncharacterized LysR-type transcriptional regulator (LTTR) CrgA-like 3. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	8.05908e-98
NZ_CP021768.1|WP_087922709.1|2421573_2421951_+|copper-homeostasis-periplasmic-binding-protein-CopC	gnl|CDD|377255	pfam04234, CopC, CopC domain. CopC is a bacterial blue copper protein that binds 1 atom of copper per protein molecule. Along with CopA, CopC mediates copper resistance by sequestration of copper in the periplasm.	1.74785e-23
NZ_CP021768.1|WP_087922705.1|2418427_2418961_-|DUF2796-domain-containing-protein	gnl|CDD|378529	pfam10986, DUF2796, Protein of unknown function (DUF2796). This bacterial family of proteins has no known function.	5.30542e-30
NZ_CP021768.1|WP_049396107.1|2410665_2411202_-|peroxidase-related-enzyme	gnl|CDD|130981	TIGR01926, peroxid_rel, uncharacterized peroxidase-related enzyme. This protein family with length of about 200 amino acids. One member, from Myxococcus xanthus, is a selenoprotein, with an otherwise conserved Cys replaced by Sec. This family is drawn narrowly enough to suggest that These proteins contain a domain described by TIGR00778, with a CxxCxxxHxxxxxxxG motif. Some members of that family are known to act as peroxidases or correlate with resistance to oxidative stress.	5.02226e-21
NZ_CP021768.1|WP_087922715.1|2426796_2429874_-|efflux-RND-transporter-permease-subunit	gnl|CDD|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP021768.1|WP_087922703.1|2416489_2417743_-|ABC-transporter-permease	gnl|CDD|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	1.86286e-09
NZ_CP021768.1|WP_087922697.1|2411308_2412190_+|AraC-family-transcriptional-regulator	gnl|CDD|378976	pfam12852, Cupin_6, Cupin. This is a family of bacterial and eukaryotic proteins that belong to the Cupin superfamily. Some of the proteins in this family are annotated as being members of the AraC family of transcription factors, in which case this domain corresponds to the ligand binding domain.	1.09128e-26
NZ_CP021768.1|WP_087922716.1|2429870_2431043_-|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	1.3271e-37
NZ_CP021768.1|WP_087922714.1|2425952_2426696_+|SDR-family-oxidoreductase	gnl|CDD|187620	cd05362, THN_reductase-like_SDR_c, tetrahydroxynaphthalene/trihydroxynaphthalene reductase-like, classical (c) SDRs. 1,3,6,8-tetrahydroxynaphthalene reductase (4HNR) of Magnaporthe grisea and the related 1,3,8-trihydroxynaphthalene reductase (3HNR) are typical members of the SDR family containing the canonical glycine rich NAD(P)-binding site and active site tetrad, and function in fungal melanin biosynthesis. This subgroup also includes an SDR from Norway spruce that may function to protect against both biotic and abitoic stress. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.0808e-113
NZ_CP021768.1|WP_087922707.1|2419622_2420525_-|LysR-family-transcriptional-regulator	gnl|CDD|176167	cd08478, PBP2_CrgA, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA, contains the type 2 periplasmic binding domain. This CD represents the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.28779e-118
NZ_CP021768.1|WP_087922701.1|2415313_2415946_-|DUF3299-domain-containing-protein	gnl|CDD|378700	pfam11736, DUF3299, Protein of unknown function (DUF3299). This is a family of bacterial proteins of unknown function.	4.2844e-41
NZ_CP021768.1|WP_087922699.1|2412854_2414387_-|MFS-transporter	gnl|CDD|184957	PRK14995, PRK14995, SmvA family efflux MFS transporter.	3.85208e-87
NZ_CP021768.1|WP_087922698.1|2412292_2412850_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	2.65318e-09
NZ_CP021768.1|WP_087922712.1|2423586_2424954_+|heavy-metal-sensor-histidine-kinase	gnl|CDD|273593	TIGR01386, Probable_sensor_protein_PcoS, heavy metal sensor kinase. Members of this family contain a sensor histidine kinase domain (pfam00512) and a domain found in bacterial signal proteins (pfam00672). This group is separated phylogenetically from related proteins with similar architecture and contains a number of proteins associated with heavy metal resistance efflux systems for copper, silver, cadmium, and/or zinc.	2.74966e-111
NZ_CP021768.1|WP_087922704.1|2417735_2418431_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	1.92725e-69

Protein sequences

>NZ_CP021768.1|WP_087922705.1|2418427_2418961_-|DUF2796-domain-containing-protein
MKRSAALFLLLAASAAQAHDVRQLGAHVHGQATVDLALDQQTLEFALQAPGIGILDFERPPANAAEQAALARAIALLKDGRWVTLPTAAGCRLSGNDAKAEGFDAMATPPPAGQHRHAGFSATLQYHCARPAELRAIVVRLPALFPGLHEVIVNSATPHGQNRSVLTPDNLRVVLAP
>NZ_CP021768.1|WP_087922704.1|2417735_2418431_-|ATP-binding-cassette-domain-containing-protein
MSMRPVIALDDVQFGYGRRLVLDVPRLWIEQGSSVLLRGISGGGKSTLLGLLAGVLLPAKGSVEVAGHALQAMRGAARDRFRADHLGVIFQQFNLLPFLSVRDNIALGLRFSRLRSERISGSVDAEIVRLLRALQLDPALMQRRSGRLSVGQQQRVAAARALIGRPALLLADEPTSALDREAATAFLELMSAQCQAAGTTVLVVSHDDSLQPLFDRTISLSEINQAGAGHA
>NZ_CP021768.1|WP_087922703.1|2416489_2417743_-|ABC-transporter-permease
MLELAWASLRSRALSVGLTVLVITLSVVLLLGVERVRTQAHEGFASTVSGTDLIVGARSGPVNLLLYSVFHIGDPTNNVSWQSYQALSAMPQVKWAVPLSLGDSWRGYRVVGTSGGYFEHYRYGAGHALAFAQGRAFDDLYDAVIGADVARAQKVGLGDEIVLAHGTGAVTLAMHADKPFRVSGILQRTGTPVDSSLLVSLPAIEAIHLDWRSGVQLRSQSVSAEQARHLDLTPTSITAFMLGLNSRIATFSVQRRINEYPEEAMLAILPGVTLQQLWQSLGTAERALQLISAMVVLLGMVSLVALLVSTLQERRREMAILRATGARPGYIAGLLVVEAVATSAVACVLALALLVAASIAGRGWALATFGLSITHVWPDGRELAWVAGVLAISTAAGLVPALLAYRRTLADGLSPGG
>NZ_CP021768.1|WP_087922702.1|2415935_2416487_-|DUF3299-domain-containing-protein
MRWLPMLPMLLVLAACERPVDTGVQALPPSPVVDRDDPAGATEQELDWLQMMPKDELAALERGEGPEVEHNGNRRMPQFGTFRTVETVLQRPVRLPGYVVPLANAQDGRLTEFLFVPYYGACIHVPPPPPNQIVHVVLPRPIAMPDMYSPFFLAGTLRAERLDDDLAGSAYTMRDAQLRPYEP
>NZ_CP021768.1|WP_087922701.1|2415313_2415946_-|DUF3299-domain-containing-protein
MNRNVLIGLTCCLGLLGCTQAGGDATTVAAAPAPAAVPAQPVAAEAPIDRWDALRPDEVTYQRPPPQIGLSRNGMDGVGGLIDDTGSGTPPGQEIDHSSPDRAKQFGSSQVVDAADGRTVDLDGYVVPLGTNDAGLVDELLFVPFYGACIHVPPPPPNQIIHVTLARPIALGDLWDPYRLAGRLQVKRFDADIASASYDAAAATLTAIHN
>NZ_CP021768.1|WP_087922700.1|2414567_2415314_-|hypothetical-protein
MRVRWTIVAAALLVAVALLVWWQRQAAPIAPPAIAFPPPSSGARQRIEQRLGDDHAFRNDVLFLLAATLRDRCQPAQAGLLARMANRASLPVLAAISTVTQQDPSLDQPIYQYIQHRADATPCGQPLQMPLAGGHSMAVDIEQYARTFPDSYFDPQRSSEPRDFGGLSLQQRAGNACNSVVYSVLPLGGTDWRCSSLRANARARVRRLCEDELRRQHGGTGGELDMAVGQGMQAAVVSAIAALPEDCR
>NZ_CP021768.1|WP_087922699.1|2412854_2414387_-|MFS-transporter
MALSQPLAGAPALSRARRWALLFTVAAGLLLVTLDNSVLYTALPTLTEELSASAGQALWIINAYPLVMAGLLLGAGTLGDRIGHRRMFLIGLVVFGIASLAAAFADTATQLIAARAFLAVGAAAMMPATLALIGLSFHEERERNIAIAIWGSVAIVGAALGPIIGGWLLQHFWWGSVFLINVPVVVVAFVATLLLAPEGQRDISRPWDLVSSVLALAALSGLVLAIKSLIATPPSYALGAGALLLAVISGAAFARRQQQLPYPLLDFAIFRNPAFLAGTLSAVFTLFAMAGLQLVTTQRFQLVAGFTPLQAGLLVSVAALGSLPSALLGGSILHRVGLRPLICGGLAAGALGVGVVAFGFPHGLGWVVAGMAITGFGMGSAISVASTAILNNVPAHRAGMASSVEEVSYEFGGLLAVAMLGSLSAAMYGAFLPASADMPELAREGFTQALHVARESGQGEWFALATAAYDRGYQIVLLVITVMLALGATIIARLLRGRVGSREGAADRVK
>NZ_CP021768.1|WP_087922698.1|2412292_2412850_-|TetR/AcrR-family-transcriptional-regulator
MRTSKRERILDAAVNVINRDGVRAVTFESVAAEAKLTRGGLLYHFPSREALLRGIDEHLVQAWETSMESLLGKRAEEASALERYQTFVRVSAQSATRAELMFMLESADPDAEERPWGPAVRRWAPLPPSAGQDDPAALDNFVARLAADGLWIYEAMYEGQLDESVRGQVAERIAGLLAKPDGASS
>NZ_CP021768.1|WP_087922697.1|2411308_2412190_+|AraC-family-transcriptional-regulator
MHLPADTSAPDRLSSLLERFRVQAALFHSGPLCGRHVFAPQPGRAFLHILRRGEMEVRHPDGDTALPRLKIDVPSLLLYPQPLHHVFFNAPLEGPDFTCATLDFDGGARNPIVQSLPPVMVVPLAAIGELDDTLHLLFAEADRRRCGSRLLTNRLFEVALIQILRWVVDHPDAAGVSHGLMRGLSDARLARTLVAMHQAPQDEWTLPRMAATAGMSRSAFAAVFKEMMQATPASYLLDWRLSLACAQLRAGVAVKQVAIEVGFADTASLSKAFRKRLGASPRAWLAATAAQAG
>NZ_CP021768.1|WP_049396107.1|2410665_2411202_-|peroxidase-related-enzyme
MSRVPLIDAANTTADRQALLGQVHAAFGATPAMFRAVANSPAALQSMWGSFGALGGGRLSPLLGEQIAVAIANRNACEYCLAAHTALGRKAGASSEQMAAAQIGQSSDPATSAALDFALKVVEQRAQIADGDVQALRAAGFDDEQIVEILAHVALNLFTNYVNVAFDVPVDFPKVALR
>NZ_CP021768.1|WP_087922707.1|2419622_2420525_-|LysR-family-transcriptional-regulator
MKTTLDELKAFVAVVDSGSITAAAEGLELTISATSRTLARLEDKLQTTLLRRTTRRLELTEEGAAFLEYARTILATVDEAEEQMAARRLQPVGRLRVDAATPFMLHVIVPLLEGFRERYPQVELELNSNEGITDLIEKRTDVAFRIGVLRDSTLHARPIGHSRIRVVASPEYLRRHGTPTRVEQLRTHDLLGFTQPSSLNEWPLLDDDGGPFVIEPAIASSSGETLRQMAVAGLGIACLSDFLTRQDRREGRLVQLFARQTQDVRQPINAVYYRNTALAARITCFVDHVTQTLGQRPFDE
>NZ_CP021768.1|WP_087922708.1|2420643_2421447_+|2,5-didehydrogluconate-reductase-DkgB
MSVPSFGVGTFRLTGQTVIDSVRNALELGYRAIDTAQIYGNEAEVGQAIAESGVPRDQLFLTTKIWVDNYAADKLIPSLRDSLAKLRTDHVDLLLIHWPAPGNGVELREYMTALAEAKTLGLTRQIGVSNFNITLTRQAIEVVGAGEIATNQIELSPYLQNPALTAFLQDQGIAVTSYMTLAYGKVLKDPVLAAIADKHHATVAQVALAWALQRGYSVIPSSTKRENLASNLLAQDLRLDDDDMAAIAALERNGREVDPPGLAPAWD
>NZ_CP021768.1|WP_087922709.1|2421573_2421951_+|copper-homeostasis-periplasmic-binding-protein-CopC
MTRSLFRRASLILLLSSLAVAPLALAHPSLVRSTPAADASVAPASQIELQFSEKVMPRATRIELSMDHGRMKMAMPTTAQDISEDGHTLRARFAKPLPAGSYALQWRAVGQDSHPITGSYRFTVK
>NZ_CP021768.1|WP_087922710.1|2421961_2422846_+|copper-homeostasis-membrane-protein-CopD
MAELSPYALRLALYLVLMLLFGRILFARPALPRGVLLALALIALLVGVTDAVARLSSVLGLSPADIDLDMARWFLTGTPVGEAGLLRLLALLAMLPLLAFAAPLQGLRRVALVALSGTALASLSWNGHAAAGDGFGGTVRLVAGIVHLLAAGAWVGALAAILQLALRPQGLRLRERTHELWQAAHRFALPGTIIVATLAMTGTYTYVDLGGSLQTLTGTAHGRWLLLKLALVGGMLGLAALHRWRLVPALATSIRGGWQPRPLRSLRHSLACESVLALLVLACVAVLGTLDPLT
>NZ_CP021768.1|WP_087922711.1|2422891_2423590_+|heavy-metal-response-regulator-transcription-factor
MKLLIVEDEPKTGNYLRQGLIEAGYVVDLACNGVDGLHLAGSGEYQLLILDVMLPGLDGWNVLSRLREAGWQVPVLFLTARSSIADRVQGLELGADDYLGKPFAFAELLARVRTLLRRGQALPQAERIVIADLVVDTLRRRVERAGQRITLSPKEYTLLELLARRRGEVLPRSLIASQVWDMNFDSDTNVIDVAIRRLRAKIDDGFDARLIVTVRGMGYVLETPDDGAAHSG
>NZ_CP021768.1|WP_087922712.1|2423586_2424954_+|heavy-metal-sensor-histidine-kinase
MNLRRSIAVRLTLLFATVATLVLAALGVAIYVSARHDLVAQDFIDLENKVALIRDLAGNGPASARGPRLAEALGHHPDIAFHIVDGRGGVLFSTAPALLREHARSQPIDAAPRRHDWILADGRCMHALHLRQTLADGSQLVTLVAIDDDRHADFLQRFRHLLAIAIIGAAVASSLLGGYVVRRTLRPLRTLADEARQITAGRLQRRLSARSAPAELEQLAQTLNGMLARLQQDFARLTGFSGDLAHELRTPITNMLTQVQVVLAHPRSNEAYRETLVSCAEELQQLAQTVGDLLYLAQAEAPGALPSRELVALDVVVDSLLEFYDLLAEDQQLTLHREGTACVEGNRLMLHRAIANLLSNALKHAALGSDVRVRLVEHGDLCRISVHNIGPPIAEEALPRLFDRFYRGERGRHEGAGLGLAITRAIAQAHGGTVNVTSDETGTVFELALPSASAR
>NZ_CP021768.1|WP_087922713.1|2424934_2425846_-|LysR-family-transcriptional-regulator
MDRFTAMRAFVRIVERRSFTRASEDLGLPRATVTDAIKALEQRLGVRLLHRTTRLVVPTLEGEAFYGRCLRLIADMDDAEAAFRDVPPRGPLRIEVHGTLGRHLLFPHLPDFLQRYPEIELEVSEGDRYVDLLREGVDAALRVGTLADSDLAARRLTLLREITVASPGYVQAYGMPGTIESLEQGHRMVGYRSSATGQLIPLEFQQGAQVRHVPLPVSVRVSGADAFLGAALAGLGIIQAPRYRMDPYIGSGQLVELLPDLPPTPSPLSLVYPRNRTPSPRLRVFIDWVAGVFGPAGINGLMR
>NZ_CP021768.1|WP_087922714.1|2425952_2426696_+|SDR-family-oxidoreductase
MTLSPTRSVALVTGGSRGIGAAISRRLAADGHAVVINYAGRRDDAEALAAELNAAGAQALALQADVADPQAVHQLFDAIEARFGGLDVVVNNAGVLQLAPLADSDDALFERVIGINLKGAFNVLRESARRVRDGGRLISLSTSVVGIRLENYSVYAASKAAVETMGAILSKELRGRDITVNAVAPGPTATALFLEGKSPELIERLAKMNPLERLGTPEDIAGAVAFLAGADGRWINGQVLRANGGMV
>NZ_CP021768.1|WP_087922715.1|2426796_2429874_-|efflux-RND-transporter-permease-subunit
MIDRLIAYCLRQPLMVMLALLLFIGAGIAAFRVLPVEAFPDVSDTQVTVVSLHPGRAAEEVEREVTMPLEVALSGIPHSVRVFSHTQFGLSMIILTFDDKADDYFARQQVLERLQGVELPEGVTPELEAMSSAVGEIYRYVLKGPHMTPTQLRTVQEWTMERSLRTVPGVADVISFGGFARTFQVKPDLDKLRDRGISLGEFAEALEKGSSNAGGGYVERGQQQFLIRGVGLMRSPADIGNVVVEQRGGTPILVRDLASIADTGLPRQGLVGQDQNDDAVFGMVLMRKGENPSDVLDALHARIAEIQANQLPAGVSIEPFYDRSWLVSTTLKTVFRNLLEGAVLVFLVLWLFLYNARAALIVAAMMPLALLSTFLGLHLWGVPANLLSLGAMDFGIIIDGAVIVTEHIVSRLSKLPPTADRKTRFSTILSAASEVGRPTFFSMLIIIAAHIPIFTLQRQEGRMFAPMAYSVTSALIGALILALTVVPLFCYWWLRRDRMRDGNPLMDRLTGWYRPILERALARPRAVVLTAVALLVGTLALGTRLGSEFLPELDEGSIWLTATLDPSTSLAEAQQQSRRIRELVGTFPQVSTVVAKLGRPEDGSDAKGANQIEALVALKPEKEWPKGVDKRQLVSDLQRSLEQRIPGPEFSISQPVRDNILESISQIKGQVVIKVSGSDLDVLNQHAQAILGQVRGVDGVESAFIDRDGSLPQLQIEIDRDRAARYGLNVRDIDEVIETALGGRQVGELWEGDRKFPITLRLDDADRDLQRLRTVPVGIGDGHAVTLSDVADFRMASGAINISRENAQRVKAVSIFIAGRDMGSVVADMRKRVDATVQLPEGYRLEWSGEFENQQRAMKRLGWVIPLSVLIIFVLLFDAFKDISSAALILANVPLAMIGGILALWLTGIPLSVSAAIGFIALFGQAVLNGVVMLSRFAQLREQGMDLLQSVVQGSLQRLRTVLMTALLAMFGLLPMATSHAIGAETQKPLAVVVIGGLLSAMLLTLLVLPTLYYWVHRRREARTG
>NZ_CP021768.1|WP_087922716.1|2429870_2431043_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MKSTVAHRLRARHALLPALLALALLGGCGREPASYAEDAPQVSAGQIQFPADSRQLDVLRSEAVTVGASASLQLPGRVVWDETRSSALRTPLAGQVARIEAQPGQKVKAGQVIAWITSPEFGQAQADGVRGRAELQQARRELERTRELHAAGVASGRELDEAEANFAGSQADHARATAFARAYGNGQHVDQRLPLRAPIDGVLVERRMSPGMAVSPDSEQPLAVVGDPDRLWLLLDVPESLAGRLKAGMQVSVPGADGQPLQATLQHVDDFVDSERRVVQARAELDNRARGFKAGQYVRAQVALPAEGGVSLPDAAVLLIDGKQVVFVEEGKGRFVRHAVHAEELGDGRLWVREGLPVGSRVVVEGGLLLQQLVDSAPAAASTGAGHAAP

Crispr_ID: NZ_CP021768_6

• CRISPR_ID: NZ_CP021768_6
• CRISPR_location: 2471850-2471954
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_6

Consensus_repeat	Method
CATCCACGCATGGCGTGGATCTACTGC	CRISPRCasFinder

spacers of NZ_CP021768_6

>6.1|2471877|51|NZ_CP021768|CRISPRCasFinder
TGAGGCTGCTCTGGTGGGTGCCGACCTTGGTCGGCACTGAGCCAGCCCCGC

CRISPR arrays and Neighbor proteins around NZ_CP021768_6

CRISPR arrays

The CRISPR arrays of NZ_CP021768_6

>merge|NZ_CP021768|6|2471850-2471954|CRISPRCasFinder
CATCCACGCATGGCGTGGATCTACTGCTGAGGCTGCTCTGGTGGGTGCCGACCTTGGTCGGCACTGAGCCAGCCCCGCCATCCACGCATGGCGTGGATCTACTGC

>NZ_CP021768|6|5|2471850-2471954|CRISPRCasFinder
CATCCACGCATGGCGTGGATCTACTGC	TGAGGCTGCTCTGGTGGGTGCCGACCTTGGTCGGCACTGAGCCAGCCCCGC
CATCCACGCATGGCGTGGATCTACTGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087922748.1|2471216_2471831_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl|CDD|227132
NZ_CP021768.1|WP_087922747.1|2470857_2471220_+|type-II-secretion-system-minor-pseudopilin-GspI	unknown	unknown	gnl|CDD|273767
NZ_CP021768.1|WP_087924182.1|2469834_2470299_-|general-secretion-pathway-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922749.1|2472189_2484573_-|filamentous-hemagglutinin-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|372178
NZ_CP021768.1|WP_087922751.1|2486202_2487402_-|type-II-secretion-system-inner-membrane-protein-GspF	unknown	unknown	gnl|CDD|273980
NZ_CP021768.1|WP_087922752.1|2487409_2488843_-|type-II-secretion-system-ATPase-GspE	unknown	unknown	gnl|CDD|131585
NZ_CP021768.1|WP_087924183.1|2492901_2493807_-|type-II-secretion-system-minor-pseudopilin-GspK	unknown	unknown	gnl|CDD|377165
NZ_CP021768.1|WP_087922753.1|2488839_2491221_-|type-II-secretion-system-secretin-GspD	unknown	unknown	gnl|CDD|274175
NZ_CP021768.1|WP_087922746.1|2470414_2470861_+|type-II-secretion-system-minor-pseudopilin-GspH	unknown	unknown	gnl|CDD|130769
NZ_CP021768.1|WP_087922755.1|2491741_2492905_-|general-secretion-pathway-protein-GspL	unknown	unknown	gnl|CDD|273768
NZ_CP021768.1|WP_087922750.1|2484772_2485948_-|alkaline-phosphatase	unknown	unknown	gnl|CDD|270283
NZ_CP021768.1|WP_087922743.1|2465769_2467554_-|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl|CDD|227622
NZ_CP021768.1|WP_087922742.1|2464640_2465306_-|TonB-family-protein	unknown	unknown	gnl|CDD|223880
NZ_CP021768.1|WP_005409874.1|2465345_2465759_-|biopolymer-transporter-ExbD	unknown	unknown	gnl|CDD|223917
NZ_CP021768.1|WP_087922741.1|2462852_2464598_-|hypothetical-protein	unknown	unknown	gnl|CDD|374891
NZ_CP021768.1|WP_087922745.1|2469410_2469746_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922744.1|2467592_2469209_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	unknown	unknown	gnl|CDD|225387
NZ_CP021768.1|WP_087922756.1|2493816_2494254_-|type-II-secretion-system-major-pseudopilin-GspG	unknown	unknown	gnl|CDD|130771
NZ_CP021768.1|WP_087922757.1|2494311_2494893_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087922754.1|2491217_2491745_-|general-secretion-pathway-protein-GspM	unknown	unknown	gnl|CDD|377391

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087922748.1|2471216_2471831_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl|CDD|227132	COG4795, PulJ, Type II secretory pathway, component PulJ [Intracellular trafficking and secretion].	3.49279e-15
NZ_CP021768.1|WP_087922747.1|2470857_2471220_+|type-II-secretion-system-minor-pseudopilin-GspI	gnl|CDD|273767	TIGR01707, Type_II_secretion_system_protein_I, type II secretion system protein I. This model represents GspI, one of two proteins highly conserved at their N-termini and described by pfam02501 but easily separable phylogenetically. The other is GspJ. Both GspI and GspJ are proteins of the type II secretion pathway, or main terminal branch of the general secretion pathway. This pathway carries proteins across the outer membrane. Note that proteins of type II secretion are cryptic in E. coli K-12 - present but not yet demonstrated to act on any target.	4.36464e-15
NZ_CP021768.1|WP_005409874.1|2465345_2465759_-|biopolymer-transporter-ExbD	gnl|CDD|223917	COG0848, ExbD, Biopolymer transport protein [Intracellular trafficking and secretion].	8.7853e-35
NZ_CP021768.1|WP_087922749.1|2472189_2484573_-|filamentous-hemagglutinin-N-terminal-domain-containing-protein	gnl|CDD|372178	pfam12545, DUF3739, Filamentous haemagglutinin family outer membrane protein. This domain family is found in bacteria, and is approximately 110 amino acids in length. The family is found in association with pfam05860.	4.2864e-44
NZ_CP021768.1|WP_087922751.1|2486202_2487402_-|type-II-secretion-system-inner-membrane-protein-GspF	gnl|CDD|273980	TIGR02120, Putative_general_secretion_pathway_protein_F, type II secretion system protein F. This membrane protein is a component of the terminal branch complex of the general secretion pathway (GSP), also known as the"Type II" secretion pathway. The GSP transports proteins (generally virulence-associated cell wall hydrolases) across the outer membrase of the bacterial cell. Transport across the inner membrane is often, but not exclusively handled by the Sec system. This model was constructed from the broader subfamily model, pfam00482 which includes components of pilin complexes (PilC) as well as other related genes. GspF is nearly always gene clustered with other GSP subunits. Some genes from Xylella and Xanthomonas strains score below the trusted cutoff due to excessive divergence from the family such that a sequence from Deinococcus which does not appear to be GspF scores higher. [Protein fate, Protein and peptide secretion and trafficking].	2.50868e-159
NZ_CP021768.1|WP_087922752.1|2487409_2488843_-|type-II-secretion-system-ATPase-GspE	gnl|CDD|131585	TIGR02533, Type_II_secretion_system_protein_E, type II secretion system protein E. This family describes GspE, the E protein of the type II secretion system, also called the main terminal branch of the general secretion pathway. This model separates GspE from the PilB protein of type IV pilin biosynthesis. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	0
NZ_CP021768.1|WP_087924183.1|2492901_2493807_-|type-II-secretion-system-minor-pseudopilin-GspK	gnl|CDD|377165	pfam03934, T2SSK, Type II secretion system (T2SS), protein K. Members of this family are involved in the Type II protein secretion system. The T2SK family includes proteins such as ExeK, PulK, OutX and XcpX.	7.8632e-33
NZ_CP021768.1|WP_087922753.1|2488839_2491221_-|type-II-secretion-system-secretin-GspD	gnl|CDD|274175	TIGR02517, Putative_type_II_secretion_system_protein_D, type II secretion system protein D. In Gram-negative bacteria, proteins that have first crossed the inner member by Sec-dependent protein transport can be exported across the outer membrane by type II secretion, also called the main terminal branch of the general secretion pathway. Members of this family are general secretion pathway protein D. In Yersinia enterocolitica, a second member of this family is part of a novel second type II secretion system specifically associated with virulence (See ). This family is closely homologous to the type IV pilus outer membrane secretin PilQ (TIGR02515) and to the type III secretion system pore YscC/HrcC (TIGR02516). [Protein fate, Protein and peptide secretion and trafficking].	0
NZ_CP021768.1|WP_087922746.1|2470414_2470861_+|type-II-secretion-system-minor-pseudopilin-GspH	gnl|CDD|130769	TIGR01708, Type_II_secretion_system_protein_H, type II secretion system protein H. This model represents GspH, protein H of the main terminal branch of the general secretion pathway, also called type II secretion. It transports folded proteins across the bacterial outer membrane and is widely distributed in Gram-negative pathogens. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	2.84552e-20
NZ_CP021768.1|WP_087922755.1|2491741_2492905_-|general-secretion-pathway-protein-GspL	gnl|CDD|273768	TIGR01709, Type_II_secretion_system_protein_L, type II secretion system protein L. This model represents GspL, protein L of the main terminal branch of the general secretion pathway, also called type II secretion. It transports folded proteins across the bacterial outer membrane and is widely distributed in Gram-negative pathogens. [Protein fate, Protein and peptide secretion and trafficking].	2.19236e-18
NZ_CP021768.1|WP_087922750.1|2484772_2485948_-|alkaline-phosphatase	gnl|CDD|270283	cd13565, PBP2_PstS, Substrate binding domain of ABC-type phosphate transporter, a member of the type 2 periplasmic-binding fold superfamily. This subfamily contians phosphate binding domain found in PstS proteins that serve as initial receptors in the ABC transport of phosphate in eubacteria and archaea. After binding the ligand, PstS interacts 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. The PstS proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.59062e-25
NZ_CP021768.1|WP_087922743.1|2465769_2467554_-|MotA/TolQ/ExbB-proton-channel-family-protein	gnl|CDD|227622	COG5306, COG5306, Uncharacterized conserved protein [Function unknown].	6.76268e-44
NZ_CP021768.1|WP_087922742.1|2464640_2465306_-|TonB-family-protein	gnl|CDD|223880	COG0810, TonB, Periplasmic protein TonB, links inner and outer membranes [Cell envelope biogenesis, outer membrane].	5.09917e-08
NZ_CP021768.1|WP_087922741.1|2462852_2464598_-|hypothetical-protein	gnl|CDD|374891	pfam16930, Porin_5, Putative porin.	0
NZ_CP021768.1|WP_087922744.1|2467592_2469209_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein	gnl|CDD|225387	COG2831, FhaC, Hemolysin activation/secretion protein [Intracellular trafficking and secretion].	2.52278e-77
NZ_CP021768.1|WP_087922756.1|2493816_2494254_-|type-II-secretion-system-major-pseudopilin-GspG	gnl|CDD|130771	TIGR01710, Type_II_secretion_system_protein_G, type II secretion system protein G. This model represents GspG, protein G of the main terminal branch of the general secretion pathway, also called type II secretion. It transports folded proteins across the bacterial outer membrane and is widely distributed in Gram-negative pathogens. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	5.24524e-58
NZ_CP021768.1|WP_087922754.1|2491217_2491745_-|general-secretion-pathway-protein-GspM	gnl|CDD|377391	pfam04612, T2SSM, Type II secretion system (T2SS), protein M. This family of membrane proteins consists of Type II secretion system protein M sequences from several Gram-negative (diderm) bacteria. The precise function of these proteins is unknown, though in Vibrio cholerae, the T2SM (EpsM) protein interacts with the T2SL (EpsL) protein, and also forms homodimers.	1.3009e-14

Protein sequences

>NZ_CP021768.1|WP_087922748.1|2471216_2471831_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MKRVTRGFTLIEVMIAITIMGVLALICWRALDSVASSDQRLRRADAETTTALRVLQQFQRDIDMRADDALMNGAVRPADQPQRLLPPSLVSERHPDGSFALEITRSVGSDGLRWQRVRWWRQGNTLWRASGEATDRYPLPAPEQSRGIAVARDVQRFEVRAWQPGAGWAVLPGEGEVLPATGLELRLGLRDGRGPLSYRRVLEL
>NZ_CP021768.1|WP_087922747.1|2470857_2471220_+|type-II-secretion-system-minor-pseudopilin-GspI
MKRNMRGFTLIEVLIALAIVSIALAAVMRSVAVATDDQSRLRDRRLALLCVQDRWQELRLAGQPPQDARLRCVQGRSTFLVLQHLGTGSDSQPQLELSVVAEDAPRQSLARMQLPWTPTQ
>NZ_CP021768.1|WP_087922746.1|2470414_2470861_+|type-II-secretion-system-minor-pseudopilin-GspH
MQHVPRGFTLLELMVVLVIIGICTAGIGLGLGSLLDPGRQLRQEAERLAQRLQVARDEARIDGRPWRWQADAAGYRFSRREGARWVDVQRDDLLRPQPWQPAGIVVQPATPIELSPEWIGVAWELTLSLQGRQLRLRDDGSGQLQVVQ
>NZ_CP021768.1|WP_087924182.1|2469834_2470299_-|general-secretion-pathway-protein
MDGRRWDRNRMLTLLAATLLLAVVAYWSVTLSAVAPTAAASGAHAEAPARPLFDAVASLPLVRLLSPGAVQTEVVVLGVMAGDQSPLALLSVDGRPPEAYAPGQRLGPCTVLASISANVVELNQAGQSRSLPVPALPPVPSDGIVPAVPQGGAP
>NZ_CP021768.1|WP_087922745.1|2469410_2469746_+|hypothetical-protein
MNEPLKARLRPALALALLLALPSAWADKAKKQDEAAPCIEVQVNGERIPAWECLQRKLAPAPKSAKSPALPEAERLMRQPGNQLMQYNLEGTRQRMGDAFGHSVVPQRPLR
>NZ_CP021768.1|WP_087922744.1|2467592_2469209_-|ShlB/FhaC/HecB-family-hemolysin-secretion/activation-protein
MTPVPCRAVRLPLRLHPLMLALAALPLPLFAQEAAPAPSVNINEYIVRGNTVLDPRDIERAVEPFLGPGRTLADVEKARDAVHALYQQAGYQSVYVELPEQQVSGGVVLLKVQQTPIGQLRVVGTRHESPERIRERVPALAEGKVPDFDQAQKELTALNEGGRRQVMPLVREGQVPGTMDVDLQVEEKSPWRASAALNNDHSADTEKLRLSASLAYDNLWKRGHSANIGVYLAPEDTKQAKVFSASYTMPFEGTPWSLEASGYTSDSRVLNAGGQVGTGTGTNVIGNGHSIGLKLNYRLAGSSQWWRQLSLGVDFKDTEEDTQMGKDSLKTPLKYAPITLAFVGVRQGEQDQLSINTQLVAGTRRLLGYGSDATAFGQKRYWADPSFVAFKADVANTHTFGNDWQWYARGSLQVTDAPLVSAEQFAAGGMYTVRGYLSAEAIGDYGGLASLEWRTPAWSLWSGTDLRVYSFADAAYLRLRQPLPEQRDKYNLASVGLGAQLRLGEHLQLRLDYAWPYADGPVTRKDDPRLHFNISTSY
>NZ_CP021768.1|WP_087922743.1|2465769_2467554_-|MotA/TolQ/ExbB-proton-channel-family-protein
MDRLLSRVLLLLAALVALPAAAADANWWQAEWKYRKPITVDAGPQGAGLAGDPGRTPLLLRLHTGNFGFDGTQDAGNDLRFVSGDGRTVLAHQIEQFDPKLGLALVWVDVPAVSAAAPQTIWMYYGNEKAPASGNGQQVFDPDYTLVYHFAEANAPARDTTAYGNNAGAVVPPSEGAVIGRGVQLGAGPLPLPASASLAQEAGAPFTVSAWIKPGSNNAAQAIYARRDGASELVVGIENRVPFVQLNGQRSTPAQPIPEGQWAHVALTAEKGALQLYLNGRVVAQLSGELPALGTAPVVGADAPGAAQPLANFEGALDELRVSRVARPAALLLADATAQGADSRLISYGADEQSAGQSHFAFILKAMPFDAWVVVAILGLMMLLSWAIMIAKSRHFGRTSKANAVFTESFGKLSGVPLRTLSDMDRQGKAPAAMHDGSLWRIYQVAIDEMQQRHQRDGNSGYLSGATIAAIRASMDAVMVREQEAMARRMNWLSTTIEGAPYVGLFGTVIGIMLVFVVAAMAGAVDINSVAPGMAAALLCTAAGLGVAIPALFGYNYLGARAEAIGADMAVFIDEFAARLAEEQDGRGPAAVQG
>NZ_CP021768.1|WP_005409874.1|2465345_2465759_-|biopolymer-transporter-ExbD
MGQKAKFGIKKREKGINVTPFVDVLLVVLVIFILTSNASIPGIEVNLPKASNSVALEKPKTKAITIDPSGQVFLDAYPVTMAELEDRLRTERATTPDFPVIVRGDAQVQYARVVEVLDLLRRLELAQVGLVTGKAQG
>NZ_CP021768.1|WP_087922742.1|2464640_2465306_-|TonB-family-protein
MRGRALLVTVALVLVALLVLGVALWWLLFKDTASTRRPVVQPPMLALPPPPPPPPPPPEKPPEPETPPEETMPEPEPLDQPTPAEEPTPTPDNADPVTMNADAQAGGDNFGIQSGSGGGSSGVGRGGAGNATYGRYLGYLMQQAISRDDKVKRLAFQLQVNVWLATDGRLEKVELVRGSGNEEADAAVLDALRRIGKVDQAPPPSLDFPARVLIQGRRPGA
>NZ_CP021768.1|WP_087922741.1|2462852_2464598_-|hypothetical-protein
MNDHVRARTDSRRPRPARRALLCCAVLLSLAVPAGAMAAETTMVKLIKGLIASGALKPEDGQALLVQAEAEAAAAQRTEATGSAAASGGVALEAGDVRVPYVPQSVRDGIRDEVRQDVMAQAKSEGWAAPNEVAEWTKRIKVTGDVRVRSESRFFSERNSDIVSNWSSINSGNGFDTNTNTNLQLPPLLNTRQDRRNLWRIRARLGIEATIGQHTTAGVRLASGSSNGPVSTTEQLGGGLSKKDVWLDQAWLAYSPADWVTVRGGRFGNPFWTSDTLFSNDLNFDGLAANLTYDFDGGDLDLFGNLAVVPLEYTSDSSPSQSRVKTPNENKWLSGAQVGVNWRFNDDNALRAALGYYDFKNISGRLSSPCALYAGAVGCDTDWSRPAFMQKGNTLMLIRDIARNPLDPANTPTPQYVGLASAFRLATLNLRWDTQLAQGIGLRLDGDYIRNLAYDKQAMFSRANNGIVNNYGAGGTASIDTFRSGDTAWMVQATFGATELKEKGQWQALLGYKHIEADALPDAYNDPNFHLGGTNARGYYVGGAYALDARSWISGKWMAAKEVSGAPLSIDVFQLEFNTGF
>NZ_CP021768.1|WP_087922749.1|2472189_2484573_-|filamentous-hemagglutinin-N-terminal-domain-containing-protein
MSHPLPSAVHPAASMRRNHPMAWAIAVALGSMVAPASQAQQAFSPGWFAERGAAQGSAAQSGRMPNGVPIQFQLPAQQQDAARQKLQQTIDNLGTAAQAIALQQRLQEQARQARREAGFIVADGLGKDGLSVDQNPLTRGWLNARDAIQSQGSDGRVQVTVEQTADKAILNWETFNIGGNTTLNFLQNPDWAVLNRVNDPQARPSQILGQLKANGTVFVANRNGVVFGNNSQVNVRNLLAAAARISDAQFRDNGLYSPDASSSALSDAFGKVMVEQGARIATHEPTSATRGGGYVLLAGHSVENAGQIEARKGQVQLAAGDSFVIRRGVGTATNTSSTTRGNEIAPRFIAGSTAGSVRNTGLMRALEGDVTLAGRSVEQAGVAVASTTLAQRGTVHLLASASDAGSSVTLADGATTAVLIEDDGKATVLDTQRDSLIKESAEQDAIRAGARSATFDNLSQHNDRRDQSRVEIVSGGNIHFSADSLTVATGGQIIADAAARSYVDDAARVDVSGAVGVQVSMESNNVQVKVQGNELRDALDNRDSGKLTSSEVWVDRRRLVHVPAGTGGYEGERWYAAGGLLEVGGYLDNQGHSIGEWAAQGGTVLLGGREVVTHGGSRINLAGGSLDVQSGVIRQSWLRGVDGQVYRLDDAPAEMLFDGLYSGHEVKQERWGITETFRDPIVFAAQRVDNGYTVGRDAGRLIVSAPTAVLEGKVETATFQGAQQNRRPDTALDGYAQAQTAVARNAQLYLGRYDGQGRSGVFGSDVRLDDKAPTKAAWSLLAPVNEERRDTVWLDIAELSAQQWGRIDLATADRIRLDGNLRLQAGGQLNLTGSEVVLAGDIVIAGGQLSAGNLLDVQGRPTALLHDGRARTAIADGTRIDLSGEWSNASLAMPLDASGAWTDGGRLSLSNSHDVVVGAEATVDVEAGAALDLRGKGRIGKGGSISLQANSSTVTTDGSGRVQLGEGSRFSGRGQGSGSFSLGTGGQVRVGDVDLAGASLRLDPGLFGSGFAQYDINGHQGLEVADGARLVAALPGLRLTQVARMATDRATALAAWDAPLYSADPSSGRVSQRAGASISLRSDRNSVGGDLRVGKDALVAVDPGQTISLLGAGNIDVEGTLRAKGGRILIDDVRPETALYAGQRTERTWRFAEGALLDADADAISLPDPSGRLRGQVRAGGRIEIGGALDWESTAFVDNRPPEAFVVVERGARLQARGASAELDIDGQGRVRVDSDGGQIVLRSANALYLEGGMDAAAGGAGARGGTLGLAFGGSIHARGASEEVLRARAISLSQYSAPAQPLPAALEYGHAALSVEQLQAGGFDNLSVFGDIRAVGDVDLRLAQSLRIHGQGTSSLGMAVDAGQSSALRLSAPYVRLAQARWRQLAGENLQGTAAVASAGPEDHALAMQAELIDIRDVTWLPGFKHVALESRSDVRLTNGIASSGNTSALMTAGSMDVTAARLYPTTGAVGTLVAGASAQTVQTADYWADPDAVLRIHGIGAGTQPAPESARGTLRLVAATVQQGGNVQVPMGTLQLGGLIQNGTVGSRVELLPGSVTSTSGAGLSLPYGGTVDGVDWRVGTRSVSSQTPAGISSMGVTLKANEIEVAPGALLDMSGGGELTGAAFVSGRGGSVDVLRTALADANPRYEFSASGNPVYAIVPGRAGTFAPSGEEGFAAPGVGQQITVPAGVPGLAAGTYTLMPASYALQPGAFRVELGANGTSGIAQPIATGTGTWRVSGQQRTALGAAISPLLTDILLTPAAVVRRHSGYNETSYNSFAQSVADRRGESRGWQTIDALGLTLALGEGAGRADTPAIRFAGTARFGAATDNGRGGTLTATLASPAIGSLEIVDGGAQSQARDRGATFSDDALNAFLPARMMIGGQFNQVASQVAVTGQARSVAIRSGVTLNAPEVLVAAASGGSGVLVEAGATLDTLPFASANADASATLPYQVSGGLLAVSNQRLNLFTGTTGVEAGPVAIDIGGCQTACDGQTRLVSDGSIAVATDGTLQMRDSASYGTRQLGLSMAALNLGSAEAIAQAAAAGALPSGMTMNQSVLQQLLRGNDATGAPALDTLSLVARDSVNVFGSVDLDARDSATGRSGLQTLVLGAQAIRGYGAATDRARIRVDTLVWDGSLAASQAPGSDASVPPADPMVDRLGAGQLDIFTRQLQLGRAPFSRPSSEVPANRQVLGFSALNLSASEQLSFSAQGTLDVFQQRGDYLADKGWQYSGGSLGIDTPLLTADPAAQLRVRTGGNFRLQGGTGKAGGDALGSELSIDANRITLDSTIALASGRLSANAREGITLGSWAALDLAGRKVPLYDVDKFSWGGDVLLSSDTGDIRTDAASRIDVSARNNRGGRLTVTAMAGQADLAGVLQGAASGRYDAGGTLVPYDGGELVVRARQLQDFTGLNQRLTAGGVVGGRSFQIGEGDLRIGDEVKARRVDISVDAGSLTVAGRIDASGEQVGSIRLYARDQLQVDGTLDAHGTGLRVDSHGKIIDSPNRATITLGSAEGAVGLGSAAHLDLRAGSDVAVGEGPGQNDRTPRGTLKIDVPRLGSNDAAIAAASGLRIDGAADIQVNGVRRYDDAPLATTADVRGNRAQLVTQQWLDQVVDPHSVAWIDGALGNPDLQQRTAALGDVRLRPGVQVVARRSDANPDGDLTIAGDIDLSGYRYGPEANRADPSRRGFGESASLVLRAEGNINVYGSINDGFAPPPSTPDEGGWQLYEARNGSAGHTPFGGGLVVPVDGVKLQPGTEFQAGTRLNYDVPVESVTLPVGTVLPAPMVISQTLRLPAGTVLGAAVTTDSGQTLAAGTVLQEPLMLAAGARLGAGFRLRSAVQMAAQEWPAGAVLPVALRLAREVELKVGAYIPSLTKVELAGNGPVNLRPADANGNQGRNWALAPMLAEGTTSWDLTVVAGADAGAADPRSRRWGSEGSVVLADTHQGSIGTVKTEIIWVGDRALTEQASLDWIGDTSYAGRPIAELADMFGFTEDEFCAMSADYCGPAPRQVAAQGSLDYWGDESYVGTPAKDFAAMFGMTEDEFCSTAPSYCAGGGTQTEVTTYGKRAGTPAWSVLRTGKGDLELLAAGDVVMKSGFGVYTAGAPTTLGEGRDAAFNSPRAAAPRNTALLGSNLVPGSYDAALAGYQAWYPDHGGNLRVEAGRDIVGDVWTGRAESGTSERDWALYSSAAVGNWLWRQGTGSTTGVEPVPTSWWVNFGAYTNVSAAAGASPRMVGFTGFGTLGGGNLTLEAGRDAGVRDAIGDALGSIIAPRSGAIIAAVGSTGRVSDGQLHLTGGGDLQLRIGGTLNPNLRATFSGLNASRAGQNLDLNGTFSNLRGSLQLDAGRIGAMGVTLESYATLGVQRAADLFAPDAARAMGGPVLVLGDAAAQLQARGDVVLGGVADAGRVPLANYSAVLQDDGARAAGSTWFSLWTANTAVDLFSAGGDLAPGLAGPENVTGSNLGREQVQLVVRGGDDLLNYWLYPSRFSAIAAQGDIKLDRISTTPGTQDVILLAPSATGRLDVLAGGGIFAQRGATQIARSASDARLPGPFDPAFMAEQGDSSGNVTRSRHNLSVDGNIASPEASLPLFAFGPNTPLSTASAALAPSRFYAVQGDIIGLATGAQRTLNANVGQRTQLNWFEAAGAVQLRAGRDILGVSMTALNTAPTDITVAAAGRDIVHLDATIAGPGNTEISAGRQLRQEDAGSIVSLGGIVQGDTRPGASIALTAGSQQIDFAALRSRYLDPVNLADPAQSLASQPGKAVKVYDQELKQWLQQRFGVAADGDGALAAFDALPLEQQRIFLRQVYYAELREGGREYTDAEGPRFGSYLRGREAIATLMPDKDATGATIDRTGDIVMYGGSGVRTEAGGHIELMAPGGQIVVGVQGVVPPASAGLVTQGQGDIRLFSQDSVLLGLSRVMTTFGGDILAWSEQGDINAGRGSQTTLLYTPPRRVYDGWGNVILSPQAPASGAGIATLNPIAEVRPGDVDLIAPLGTIDAGEAGIRVSGNINLAALQVLNAANIQVQGESKGLPVLASVNVNALASASAAANSASQAAQDVMRKSQDEARRNQPSVISVQILGFGSGTSSIAPPARGTTAGSGYDADSAFQFPQASRDEGTQRR
>NZ_CP021768.1|WP_087922750.1|2484772_2485948_-|alkaline-phosphatase
MNKYKTLAALVATALLATVGAASAQTVTGGGASLPADLYKGSSDSILPANFTYAVTGSGTGKKAFLENNSLLFSTTGTVHFAGSDSVLSSTELSTYTTNFNQPTNANRYGALIQVPSVATSVTIPFNKAGSAVDLSVAQICGVFSGAISDWSTIDSNRSGPIQVVYRPESSGTSEMFSRFLTAACAAENAETSKLVGGKFAIKSTFADLYKRDANGNLPAFLVAAPATGGTSLYNTVYAAEGRIGYVGPDVIPSVTDATKVAKVKGFSPDQVSVQATLDTVAPPTGTAAENPANWVPVFGNPSAGYPIAGYTNLVIGQCYKDSSVATSLRGFLARHYPATYTVAYEKSITDHGFIPLTKAWRDAIRNRFVLASSTAGLNNPSTCAGIGRPL
>NZ_CP021768.1|WP_087922751.1|2486202_2487402_-|type-II-secretion-system-inner-membrane-protein-GspF
MALFDYQAANAQGRIEKGQLDADSPRGARQVLRGRGLTPVQVSAARSAGSGWGTRRLSASELAWATRQLASLLAASLPLEGALSAVIEQAERPHVAQALTAVRADVRAGQRLTVALAARPRDFPPIYRALVGAGEDSGDLARVMERLADYIEERNALQAKVLTAFIYPAAISLVSVAIVIFLLSYVVPQVVTAFVQARQTLPMLTQVMLAASAFVRSWGAWAGLGIAALVVAWRLALRRPELRLRWDAMLLRVPMVGRFVLGVNSARFASTLAILLDAGVPLLRSLEAARQTLGNALLARCADDVSSRVREGAALGAALKVQKVYPPILVHLVASGEKTGSLAPLLDRAAQTISREIERRAMALTALLEPTMILVMGGVVLTIVLAVLMPIMEMNQLVQ
>NZ_CP021768.1|WP_087922752.1|2487409_2488843_-|type-II-secretion-system-ATPase-GspE
MSAAAPLPYSWVRSHGVMLSEAGGAPVLLGTADTAAWAVAELRRRHGPLPFQALDAATWQQRLGEQYRDGGDAAAVVGAAESEVDLDRLMQDMPEVTDLLDAQDDAPVIRMINALLAQAARDGASDLHIEPFETHSVVRYRVDGTLRDMVQPRRALHAALVSRIKIMAHLDIAEKRLPQDGRIAIRVGGRPLDIRVSTVPTGHGERAVLRLLEKDAGRLQLQRLGMADDTLATFTGLIRQPHGIVLVTGPTGSGKTTSLYAALGQLDSSTSNILTVEDPVEYDFAGIGQIQVNARIGMSFGTALRAILRQDPDTIMIGEIRDLETAQIAVQSSLTGHGVLASLHTNDAISAVTRLADMGVEPFLLASSLRGVLAQRLVRRLCTQCRRAEVDGDGRTVWRAVGCAACANSGYRGRTGIHELFVVDDRVRALIHEGQGEPALREAARRAGMRTLRQDGQRWVDSGVTTLEEILRVTGDD
>NZ_CP021768.1|WP_087922753.1|2488839_2491221_-|type-II-secretion-system-secretin-GspD
MRAMRSLACSTALALVVGMAHVPAPVLAQGARDEPVQLNLVDTDIGGVLRMAARFTGRQFLVDPRVTGKMTVVSDGPVSRTQAYQLLLGALRMRGFAVVENGGVSRVVPQADAKLLGGRVGNGGAGGEVATRTFALRYENAAALVAVLRPMISPDNPITANPGNNTLVITDYADNLERIARVIASVDTPAGMDTDVVKLQQGIAVDVAAMVAPLLDAQGAEPSQKVVVMADPRSNSVLLRSSSPGRTRLARQLVEKLDRAQDESGNLHVVYLRNAQANQLAGVLRGVVAGQSDAPAMGSNEGITPLPGDADRSTPAQPSQPQQAKPGGSALESQRLDPNRRDPIDAESTGFSQNGISVQADVATNTLLISAPEPVYRNLRRVIDQLDQRRAQVLVESLIVEVNQTDAAELGVQWMLGNGRTFGGTHFGGVTGGSGLNTAARTTLDVLPKDGLKIGVIDGTINLPGVGQILNMKALANALQSKGGANILSTPNLMTLDNEAASIMVGQTVPFVSGRYVTDGGGGSNNPFQTIVREDVGLKLRVRPQISEGGTVKLDIYQEVSSIDAQSANSTAGIITNKRALDTSVLLDDGQIMVLGGLLEDNVSHGRDAVPGLGKIPVLGALFRSDTRKRSKTNLMVFLRPHVVRDPAAGQRLTRDRYDYMRNAQASAQPVQSWALPALSAPQLPPQDLSVLGQGNARDGQGQPLQSSSLAALYPSGDSDAQLVQFAQGLDPARASQGVAQVRALGLQAYAEATPGESGQRLRVRLPRDPATLDPALQQLRGLGYTPELVIGP
>NZ_CP021768.1|WP_087922754.1|2491217_2491745_-|general-secretion-pathway-protein-GspM
MTARTLRLGEGLEGLQQRWRRLPPRDRLMLWVMVVALLAAGLWSLWLEPLLKQHAHWQAELPRLQAQSRALAPLLRARERRQQAQGQHPTLASLRDGIRSAGLADGLHIEVRDGRWHLQVQAVPADALWNWLLPLLADPAIELQQLQLTRTGDANMPAARISGNIVMVATAGAHP
>NZ_CP021768.1|WP_087922755.1|2491741_2492905_-|general-secretion-pathway-protein-GspL
MNVQLRVRLPALECLRADSTVDWVQLRKGEVVAHGRDTLAALGLRYPKATVRACLDPHDLILLELQLPPLSGRRLQSALQGEVEAMLLDDLQEVALAHGAQAADGTVPVAWLGQQAVLQAQQLLASCALQLQALYPTPLLLPWQDAQATLQVSGEHLLVRSGRDRGFVQWYGGRDACALMRALAMRLQQAGVQAVQWIDSVPPAWPDSLPATAVRRERQACGPLPGWSLPLPGAGRQAPRLAIGLALAAVLLAALGLQLQVSRWRIEGEALQQDMARQFSARFPEITDVVDPVLQARRALAVPPPAPPLPLLQRQVASTLQAVPELAGQVRSLHYQPGQLDMELDADAQALADDPQRLEHWQQAVQVQGLQLARDAAGRLRVSGAGQ
>NZ_CP021768.1|WP_087924183.1|2492901_2493807_-|type-II-secretion-system-minor-pseudopilin-GspK
MTARTRSLPCARQRGMAVIVALLVVALVAVIATALLTRQSAQLRALRSDQLRAQVRMAVDATLERAAQQLRDDVKEQLATVRSGRWARPLTLQAPLPVQLQLVDAQSMFNLRNLLARGRPDPEARRAFIALCAAQGLGQGACASAADHIQARLRDGDIQAQAPLPRESLIAQALAGADPVALQALARRTVVLPAQTLVNANTSDLSVLQAVTPAVEPARLQALLGERDGGHWLLNRGDIANRLQLSNEQMAVLPLGIHSEWFLAVGQVQADGSAVEFRALLWREYRDDGARVQRVWTRIGA
>NZ_CP021768.1|WP_087922756.1|2493816_2494254_-|type-II-secretion-system-major-pseudopilin-GspG
MARQVGGRRARQQGFSLIEIMVVVVIIGILAALIVPRLMDRPDQARVVAARQDIAALMQALKLFKLDNGRYPSAEQGLQALVKPPQGSGAMPVTPYLDRLPNDPWGHPYQYQSPGTHGDIDVFSLGADSKPGGDAGNADIGSWQL
>NZ_CP021768.1|WP_087922757.1|2494311_2494893_-|hypothetical-protein
MADSRRISMLELDRHLSQSLEQARHTPLNVQRYGHSWVWVLSSDAWADAVRWAALDSSAHPLAALRRALDLQLRPWPEAAMSALPLEAGDVRQLQRAALLVVLRDLNSAQRVYDDLRYHQAYRMFIGLDHGTAWSPMQCVRLLQACAHPLLRGCIDETLASVSPQLFEAACVPAAAAPARAHAQRIAGGCLSY

Crispr_ID: NZ_CP021768_7

• CRISPR_ID: NZ_CP021768_7
• CRISPR_location: 2921672-2921778
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_7

Consensus_repeat	Method
CATCCACGCACGGCGTGGATCTAC	CRISPRCasFinder

spacers of NZ_CP021768_7

>7.1|2921696|59|NZ_CP021768|CRISPRCasFinder
GGGTGGGTGCCGGCCGTTGGTCGGCACGATCCTTCCGGGCCATGAACCCCGGCATCGTC

CRISPR arrays and Neighbor proteins around NZ_CP021768_7

CRISPR arrays

The CRISPR arrays of NZ_CP021768_7

>merge|NZ_CP021768|7|2921672-2921778|CRISPRCasFinder
CATCCACGCACGGCGTGGATCTACGGGTGGGTGCCGGCCGTTGGTCGGCACGATCCTTCCGGGCCATGAACCCCGGCATCGTCCATCCACGCATGGCGTGGATCTAC

>NZ_CP021768|7|6|2921672-2921778|CRISPRCasFinder
CATCCACGCACGGCGTGGATCTAC	GGGTGGGTGCCGGCCGTTGGTCGGCACGATCCTTCCGGGCCATGAACCCCGGCATCGTC
CATCCACGCATGGCGTGGATCTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087923072.1|2915318_2915768_+|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl|CDD|225039
NZ_CP021768.1|WP_087923077.1|2922919_2923801_-|DUF3298-and-DUF4163-domain-containing-protein	unknown	unknown	gnl|CDD|379356
NZ_CP021768.1|WP_087923067.1|2911162_2911504_+|arsenate-reductase-(glutaredoxin)	unknown	unknown	gnl|CDD|239332
NZ_CP021768.1|WP_005417588.1|2923838_2924141_-|N-acetyltransferase	unknown	unknown	gnl|CDD|379642
NZ_CP021768.1|WP_087923074.1|2918831_2919311_-|glutathione-peroxidase	unknown	unknown	gnl|CDD|223463
NZ_CP021768.1|WP_087923068.1|2911599_2912235_-|glutathione-S-transferase-family-protein	unknown	unknown	gnl|CDD|223698
NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_CP021768.1|WP_087923076.1|2921784_2922900_-|cyclopropane-fatty-acyl-phospholipid-synthase	unknown	unknown	gnl|CDD|183282
NZ_CP021768.1|WP_087923071.1|2914385_2915282_+|RNA-polymerase-sigma-70-factor	unknown	unknown	gnl|CDD|132002
NZ_CP021768.1|WP_014037807.1|2924555_2925182_-|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|223777
NZ_CP021768.1|WP_087923070.1|2912749_2914267_-|fumarate-hydratase	unknown	unknown	gnl|CDD|224862
NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor	unknown	unknown	gnl|CDD|240164
NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|377028
NZ_CP021768.1|WP_087923073.1|2916005_2917877_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease	unknown	unknown	gnl|CDD|238340
NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase	unknown	unknown	gnl|CDD|223678
NZ_CP021768.1|WP_006455701.1|2917957_2918737_+|ferredoxin--NADP-reductase	unknown	unknown	gnl|CDD|99792
NZ_CP021768.1|WP_087923069.1|2912292_2912628_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087923075.1|2919441_2921610_+|M3-family-metallopeptidase	unknown	unknown	gnl|CDD|341051
NZ_CP021768.1|WP_087923078.1|2925189_2926755_-|MFS-transporter	unknown	unknown	gnl|CDD|340905

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087923072.1|2915318_2915768_+|carboxymuconolactone-decarboxylase-family-protein	gnl|CDD|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	1.05541e-28
NZ_CP021768.1|WP_087923077.1|2922919_2923801_-|DUF3298-and-DUF4163-domain-containing-protein	gnl|CDD|379356	pfam13739, DUF4163, Domain of unknown function (DUF4163). The structure of this domain is and alpha-beta-two layer sandwich, identified from a Fervidobacterium nodosum Rt17-B1 like protein. The function is not known except that it is found in association with Heat-shock cognate 70kd protein 44kd ATPase, pfam11738.	1.64121e-07
NZ_CP021768.1|WP_087923067.1|2911162_2911504_+|arsenate-reductase-(glutaredoxin)	gnl|CDD|239332	cd03034, ArsC_ArsC, Arsenate Reductase (ArsC) family, ArsC subfamily; arsenic reductases similar to that encoded by arsC on the R733 plasmid of Escherichia coli. E. coli ArsC catalyzes the reduction of arsenate [As(V)] to arsenite [As(III)], the first step in the detoxification of arsenic, using reducing equivalents derived from glutathione (GSH) via glutaredoxin (GRX). ArsC contains a single catalytic cysteine, within a thioredoxin fold, that forms a covalent thiolate-As(V) intermediate, which is reduced by GRX through a mixed GSH-arsenate intermediate. This family of predominantly bacterial enzymes is unrelated to two other families of arsenate reductases which show similarity to low-molecular-weight acid phosphatases and phosphotyrosyl phosphatases.	1.56397e-50
NZ_CP021768.1|WP_014037807.1|2924555_2925182_-|rhomboid-family-intramembrane-serine-protease	gnl|CDD|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	5.19101e-16
NZ_CP021768.1|WP_087923074.1|2918831_2919311_-|glutathione-peroxidase	gnl|CDD|223463	COG0386, BtuE, Glutathione peroxidase [Posttranslational modification, protein turnover, chaperones].	2.16278e-93
NZ_CP021768.1|WP_087923068.1|2911599_2912235_-|glutathione-S-transferase-family-protein	gnl|CDD|223698	COG0625, Gst, Glutathione S-transferase [Posttranslational modification, protein turnover, chaperones].	4.67566e-39
NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	4.36479e-14
NZ_CP021768.1|WP_087923076.1|2921784_2922900_-|cyclopropane-fatty-acyl-phospholipid-synthase	gnl|CDD|183282	PRK11705, PRK11705, cyclopropane fatty acyl phospholipid synthase.	0
NZ_CP021768.1|WP_087923071.1|2914385_2915282_+|RNA-polymerase-sigma-70-factor	gnl|CDD|132002	TIGR02957, putative_sigma_factor, RNA polymerase sigma-70 factor, TIGR02957 family. This group of sigma factors are members of the sigma-70 family (TIGR02937). They and appear by homology, tree building and bidirectional best hits, to represent a conserved family. This family is found in a limited number of bacterial lineages. This family includes apparent paralogous expansion in Streptomyces coelicolor A3(2), and multiple copies in Mycobacterium smegmatis MC2, Streptomyces avermitilis MA-4680 and Nocardia farcinica IFM10152.	1.38824e-111
NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease	gnl|CDD|238340	cd00607, RNase_Sa, RNase_Sa. Ribonucleases first isolated from Streptomyces aureofaciens. In general, ribonucleases cleave phosphodiester bonds in RNA and are essential for both non-specific RNA degradation and for numerous forms of RNA processing. RNAse Sa is a guanylate specific endoribonuclease which belongs to the superfamily of microbial ribonucleases. Typical of this sub-family, the enzyme hydrolyses the phosphodiester bonds of RNA at the 3' oxygen end of guanosine residues to yield oligonucleotides with the guanosine-2',3'-cyclophosphate at the 3' end and the hydroxyl group at the 5' end. The terminal guanosine-2,3'-cyclophosphate is hydrolysed by guanyl RNAses to give guanosine-3'-phosphate.	8.67308e-43
NZ_CP021768.1|WP_087923070.1|2912749_2914267_-|fumarate-hydratase	gnl|CDD|224862	COG1951, TtdA, Tartrate dehydratase alpha subunit/Fumarate hydratase class I, N-terminal domain [Energy production and conversion].	6.54336e-146
NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor	gnl|CDD|240164	cd05141, Barstar_evA4336-like, Barstar_evA4336-like contains uncharacterized sequences similar to the uncharacterized, predicted RNAase inhibitor evA4336 found in Azoarcus sp. EvN1. This is a subfamily of the Barstar family of RNAase inhibitors. Barstar is an intracellular inhibitor of barnase, an extracellular ribonuclease of Bacillus amyloliquefaciens. Barstar binds tightly to the barnase active site and sterically blocks it thus inhibiting its potentially lethal RNase activity inside the cell. Barstar also binds and inhibits a ribonuclease called RNase Sa (produced by Streptomyces aureofaciens) which belongs to the same enzyme family as does barnase.	5.67799e-25
NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	2.51607e-08
NZ_CP021768.1|WP_087923073.1|2916005_2917877_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	3.70388e-102
NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase	gnl|CDD|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	2.19761e-109
NZ_CP021768.1|WP_006455701.1|2917957_2918737_+|ferredoxin--NADP-reductase	gnl|CDD|99792	cd06195, FNR1, Ferredoxin-NADP+ (oxido)reductase is an FAD-containing enzyme that catalyzes the reversible electron transfer between NADP(H) and electron carrier proteins such as ferredoxin and flavodoxin. Isoforms of these flavoproteins (i.e. having a non-covalently bound FAD as a prosthetic group) are present in chloroplasts, mitochondria, and bacteria in which they participate in a wide variety of redox metabolic pathways. The C-terminal domain contains most of the NADP(H) binding residues and the N-terminal domain interacts non-covalently with the isoalloxazine rings of the flavin molecule which lies largely in a large gap betweed the two domains. Ferredoxin-NADP+ reductase first accepts one electron from reduced ferredoxin to form a flavin semiquinone intermediate. The enzyme then accepts a second electron to form FADH2 which then transfers two electrons and a proton to NADP+ to form NADPH.	1.50149e-115
NZ_CP021768.1|WP_005417588.1|2923838_2924141_-|N-acetyltransferase	gnl|CDD|379642	pfam14542, Acetyltransf_CG, GCN5-related N-acetyl-transferase. This family of GCN5-related N-acetyl-transferases bind both CoA and acetyl-CoA. They are characterized by highly conserved glycine, a cysteine residue in the acetyl-CoA binding site near the acetyl group, their small size compared with other GNATs and a lack of of an obvious substrate-binding site. It is proposed that they transfer an acetyl group from acetyl-CoA to one or more unidentified aliphatic amines via an acetyl (cysteine) enzyme intermediate. The substrate might be another macromolecule.	2.58052e-26
NZ_CP021768.1|WP_087923075.1|2919441_2921610_+|M3-family-metallopeptidase	gnl|CDD|341051	cd06456, M3A_DCP, Peptidase family M3, dipeptidyl carboxypeptidase (DCP). Peptidase family M3 dipeptidyl carboxypeptidase (DCP; Dcp II; peptidyl dipeptidase; EC 3.4.15.5). This metal-binding M3A family also includes oligopeptidase A (OpdA; EC 3.4.24.70). DCP cleaves dipeptides off the C-termini of various peptides and proteins, the smallest substrate being N-blocked tripeptides and unblocked tetrapeptides. DCP from Escherichia coli is inhibited by the anti-hypertensive drug captopril, an inhibitor of the mammalian angiotensin converting enzyme (ACE, also called peptidyl dipeptidase A). OpdA may play a specific role in the degradation of signal peptides after they are released from precursor forms of secreted proteins. It can also cleave N-acetyl-L-Ala. This family also includes Arabidopsis thaliana organellar oligopeptidase OOP (At5g65620), which plays a role in targeting peptide degradation in mitochondria and chloroplasts; it degrades peptide substrates that are between 8 to 23 amino acid residues, and shows a weak preference for hydrophobic residues (F/L) at the P1 position.	0
NZ_CP021768.1|WP_087923078.1|2925189_2926755_-|MFS-transporter	gnl|CDD|340905	cd17347, MFS_SLC15A1_2_like, Solute carrier family 15 members 1 and 2, and similar Major Facilitator Superfamily transporters. Solute carrier family 15 member 1 (SLC15A1) and SLC15A2 are members of the proton-coupled oligopeptide transporter (POT) family of integral membrane proteins that mediate the cellular uptake of di/tripeptides and peptide-like drugs. They mediate the proton-coupled active transport of a broad range of dipeptides and tripeptides, including zwitterionic, anionic and cationic peptides, as well as a variety of peptide-like drugs such as cefadroxil, enalapril, and valacyclovir. SLC15A1, or peptide transporter 1 (PepT1), is primarily expressed in the brush border membranes of enterocytes of the small intestine and is also known as the intestinal isoform. SLC15A2, or peptide transporter 2 (PepT2), is abundantly expressed in the apical membrane of kidney proximal tubules and is also referred to as the renal isoform. Both proteins transport di/tripeptides, but not tetrapeptides or free amino acids, using the energy generated by an inwardly directed transmembrane proton gradient. The SLC15A1/SLC15A2-like group belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.49232e-76

Protein sequences

>NZ_CP021768.1|WP_087923075.1|2919441_2921610_+|M3-family-metallopeptidase
MTTRLALAVAMSLGLALPAFSAGAATPAASTTAQQANPFFAESPLPLHFPQFDKIKDSDFAPAFDAGMAQQLKEVEAIANNKAKPTFDNTIIALEKSGDILDRATTVFFSLVGADTNDTRKKLQADYSAKFAAHSDAIALNGKLFARIQALYDTRSQLGLDAEGVRLVEKYYDNYVRAGAKLSEADKATLKAMNAELANLGTKFSQNVQSEVNASAITVDDVKELDGLSREQIAAAAEAAKARGLEGKYVITLLNTTGQPPLTNLANRALRQKIYEASTTRGSRGGEFDNTALVSRIMQLRADKAKLMGFPNFAAYNLTNQTAKSPEAVNAMLGKLAPAAVANAKREAADLQAMIDQEQKAAGKPTFKLEPWDWAFYSEKVRQAKYNFDESQLKPYFEMKNVLENGVFYAAGQEFGLTFKQRTDLPVYHDDVTVYDVFDADGSQLAIFIFDPYARASKRGGAWMNSYVSQSKLTGFKPVVANHLNIPKPPAGQPTLLTWDEVNTTFHEFGHALHGMFSNVKYPYFSGTSVPRDFVEFPSQVNEMWADNPVILKNYAKHYQNGSAMPQALLDKVLAAAKFNQGFATTEYLGAAMLDQRWHQIGADQVPAAKDVMAFERAALEKDGIYYAPVPPRYKTPYFSHIMGGYSAGYYAYIWSEVLDANTQKWFKDNGGLSRKNGDHFRATLLSKGGSVDAMQLFRDFAGHEPQIEPLLEKRGLTGAGN
>NZ_CP021768.1|WP_087923074.1|2918831_2919311_-|glutathione-peroxidase
MTTAYDFSFRALDGQPQALARYQGQPMLLVNVASRCGFTPQYTGLEQLWQEYRERGLVVIGFPCNQFGAQEPGDAAQIRQFCSLDYPVSFPLSEKIEVNGEGADPLWAWLAREKRGLLGSARIKWNFSKFLVDRQGNVVDRFAPTTRPEQLRGAIEALL
>NZ_CP021768.1|WP_006455701.1|2917957_2918737_+|ferredoxin--NADP-reductase
MSSAFGAETVLEVRHWTDAYFSFTLTRDSGFRFENGQFVMIGLETEARPLLRAYSIASANWEEHLEFFSIKVQDGPLTSRLQHIKPGDKVLVGKKPTGTLLISDLHPGKNLYLLGTGTGMAPWLSVIKDPETYERFEKVILCHGVRYEKDLAYRDYFEKELREHEFLGEMIGDKLLYYPAVTREPFANQGRLTSLMESGEMQRTLGLPELSPENDRAMICGSPQMLADLRSVLDARGFQVSPRIGQPGHYVFERAFVEK
>NZ_CP021768.1|WP_087923073.1|2916005_2917877_+|ABC-transporter-ATP-binding-protein
MPATPTAGAAAAKKPSLRQRFRAMRNLPPFLRMVWNTSPALTLASLGLRLIRALLPVAMLYVGKLIIDSALHLSQHEAGFPPLGEALSSGMLNPLLGLLALEFGLAIASDLLGRLVSYADALLSELFANVTSIRLMEHAATLDLEDFEDPDLQDKLDRARRQTMGRMNLMSQLFGQVQDAITVASLAVGLLVYAPWLILLLALALVPAFIGESHFNAAGYSLNFQWTPERRQLDYLRQLGASVETAKEVKIYNLHRFLVERYRRLSVALFQANRSLARRRAFWGTLLAALGTLGYYTAYAYIAWRTVRGDFSIGDLTFLAGSFLRLRQLLEGLLIGFSQVASQALYLDDLFSFFQIQPEIHSREGAVRVPQPIHQGFVFENVGFRYPDAEQWAVRHLDFQLQAGEVLALVGENGAGKTTLVKLLARLYEPDEGRILLDGRDLRDYDLDDLRANLGVIFQDFVRYNLSAGENIGVGQVEAMDDHARVADAARRGMAEEVIEELPGGYNQLIGRRFKQGVDLSGGQWQKIAIARAWMRNAQVMILDEPTAALDARSEFEVFQRFRELADNRTAVLISHRFSSVRMADRILVLADGRIEASGTHEQLMAQGGRYAELFELQAAGYR
>NZ_CP021768.1|WP_087923072.1|2915318_2915768_+|carboxymuconolactone-decarboxylase-family-protein
MSDHASPRVPYTRLAAEAFKGLLATSQAVHHSSIDPTLMELVFLRVSQLNGCGYCMDMHGTALRKGGIESRKLDTLPAWHESRFFDARERAALGWAEALTRLTDGAPSQAAFDALAPHFDEKGISDLSMGIAVINAWNRLGAGLLPPLP
>NZ_CP021768.1|WP_087923071.1|2914385_2915282_+|RNA-polymerase-sigma-70-factor
MNAETAFQTHRPRLMALAYRLLGSRADAEDVVQDAWLRWSGADPAAVRDPEAWLVTATTRLGLDRLRAAKRERAHYIGPWLAEPLAVSLEPDPAPGPAQLHALADDVSVAFLTLLEQLGPEERAAFLLKEAFDHDYREIADLLGHSEANCRQLVHRARQRLQAGRPRFNADASQHRQLLARFMDASQRGDSEAIQALLHANAVLVSDGGGVVTAAVRPLLGAERIGRLFWAIARRGAAHPAQLGYVNGEPAILRFIGDRLHSITTIEVVDGRIANVYSVLNPEKLPGVVTNANGAASL
>NZ_CP021768.1|WP_087923070.1|2912749_2914267_-|fumarate-hydratase
MTSIKQEDLIQSIADALQYISYYHPVDYIKNLAAAYEREESPAAKEAMAQILINSRMCAEGHRPICQDTGIVTVFLEIGMDVRWDDATMGVEDMANEGVRRAYMHPDNKLRASVLADPAGKRVNTKDNTPGVVNVKVVPGNTVDVIVAAKGGGSEAKTKFAMLNPSDSIVDWVLKTVPTMGAGWCPPGMLGIGIGGTAEKAMLLAKEALMEPIDITELQARGASNRIEELRLELYEKVNALGIGAQGLGGLTTVLDIKINDYPTHAANLPVAMIPNCAATRHAHFTLDGSGPVMLDPPSLEDWPKLTYDASKGTRVDLDTITPEDVASWKPGQTLLLNGKLLTGRDAAHKRMVDMLNKGEQLPVDLKGRFIYYVGPVDPVRDEVVGPAGPTTATRMDKFTRQVLEQTGLLGMVGKAERGPAAIEAIRDNKSAYLMAVGGSAYLVSKAIKAAKVVGFADLGMEAIYEFTVQDMPVTVAVDSSGESVHKTGPREWQARIGKIPVVVE
>NZ_CP021768.1|WP_087923069.1|2912292_2912628_-|hypothetical-protein
MTPHRSIMAGIVLALAGCSTPASYEGAGFSASSQCRMQCQASHRSCMAQGSTGNSAFSCEQQVVPAPDKRCKDVANPELRRACELKAHDCTMRAPMMSCGERRDTCMSSCG
>NZ_CP021768.1|WP_087923068.1|2911599_2912235_-|glutathione-S-transferase-family-protein
MSTTLYGSTSTAALVVHWLLIELGIEHELVLLDFDAREHKSAEYLALNPAGVVPTLLIDGLVLTEAAAIALYLADRHPEAGLLPAQGSPQRGDAYRWMFWCANTLQPAYRAWFYPHEVAGEANVEASREMARQRLEAAWQHVATHLLAHGPYLLGATPCVADYMLVMLMRWSRNMPRPSDTWPPLKAHATAMKARPAFAEVYRREGITDWR
>NZ_CP021768.1|WP_087923067.1|2911162_2911504_+|arsenate-reductase-(glutaredoxin)
MDVTIWHNPACSNSRGALKLIRDAGFDPVVIEYLGNPPDVAALRQVLAESALSARDLVRSKETRFAELGLEDADDATLLAAMAEHPHLINRPVVRTPKGTRLCRPPETVLEIL
>NZ_CP021768.1|WP_087923076.1|2921784_2922900_-|cyclopropane-fatty-acyl-phospholipid-synthase
MDTGLQERVTGLLHEAGVRIGGTQPQDIQVHDPRFFARVMGHGSLGLGESYMEGWWDANVLDEFLVHLMQAHLDERVHGWREVADALKARLFNLQAGQGSYEVGRRHYDLGNDLYQAMLGQRLVYSCGYWRNADDLDAAQEAKLDLVCRKLGLRPGQRVLDIGCGWGEALKFAAERYGVSGVGVTISQEQAEFARELCAGLPIEIRLQDYRELDEPFDAIFSIGMFEHVGDKNYGSFFEVAKRCLSPRGLLLLHSIGTNISRHRTDPWIARYIFPNSMLPSAVQITKAFEGRFVLEDWHNFGTDYDLTLQAWRRNVEAAWPQLDAGYDEHFRRMWRFYLAGSMATFRCRHAQLWQLVLSPEGVPGGYVAPR
>NZ_CP021768.1|WP_087923077.1|2922919_2923801_-|DUF3298-and-DUF4163-domain-containing-protein
MYKHEQGIPMKIGNNRPLHGSALAGVVGVLLLAGCQRESEPVPATDAAPAAEATAASETPATEAPLDLRDVIENNEREVVGISYPAGIDRYPGLARALQSYATSARSDLQQALDGLGNDKPTMPYELSLSFEKLLETPQLVVVSADGSRYTGGAHGEPLVARFVWLPQHQQMLSAEKLVADAKGWKAISDFVADQLRERVATRLSGEDMDPAQLQESLRNASRMIADGTGPQADNFSQFQPLTDDKGQITALRFVFPPYQVGPYSDGTQTADVPAAVLLPHVAKDYVELFARG
>NZ_CP021768.1|WP_005417588.1|2923838_2924141_-|N-acetyltransferase
MASVTPPGLAYEVEHDLANHRFTARVRGQLAVLDYQIKRKRMVITHTEVPEPIAGRGIAGELTRVALRFAREQKYKVVPACSYAEAFLQRHEEYHDLLVG
>NZ_CP021768.1|WP_014037807.1|2924555_2925182_-|rhomboid-family-intramembrane-serine-protease
MTPVNLLLIAITAILSWMAFNNRKLADRLILWPPAIDRHRQYDRLVTYGFIHADWSHLIFNMITLFFFGGFIESVMVQLTGSYLTYPAFYIGALLVSILPSYLKNQKNPNYLSLGASGAVSAVLFAFILIKPWSIILVFFIPAPAIIYAAFYVGYSIWMDKRGGDRINHSAHLAGAAFGVIFMLAMQPSIFNHFLRELSNPTFRLGGG
>NZ_CP021768.1|WP_087923078.1|2925189_2926755_-|MFS-transporter
MSHDAVAPIAGQGRMPRQIPYIIGNEACERFSFYGMRNILVQFLITSLLLQEITAEGRAGEAKDIMHSFMIGVYFFPLLGGWLADRFFGKYHTILWFSLVYCAGHLCLALFENSREGFFLGLGLIALGAGGIKPLVASFMGDQFDQSNKHLAKIVFDAFYWIINFGSLFASLLIPLVLKNWGPQWAFGIPGILMFIATFVFWLGRKRYVLVPLPPKDPHSFANVVRTALTARVAGQGRPGLVIAVLGLVLAVASFGLVGSLGIVICLCLALVAILAGIGGGTWLQLDRARGQHPAEAVEGVRSVLRVLVIFALTTPFFSLFDQKASTWVLQGQQMQMPSWFTASQMQALNPLLVMILIPFNNLVLYPALRRFGFEPTALRRMTAGIAFSGLAWIVVGGIQVVMDGGNAMSIFWQMLPYALLTFGEVLVSATGLEFAYSQAPQAMKGVVMSFWNLTTTIGNLWVLLSNAAVRNDTVTHQIAGTGLSEAAFLMFFFAGFAFVAALAFGWYAKRYRMVDNYRSA
>NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein
MRPLAHARLLLSCLLLLLALQAQARPQAPTAAASESEPRQLTVAALELPSRDDAQWKQRREQVAQLLTELQPDVISVQQVLQQQGRNPACWLASRLRYSCDFVTADPPSQPLRHGNAMLTRLPVSEDGVTLLHPPGTFSAAGMMRLKLGEALVNIYVARLRPDPDEATARQHQTSDLMTWIGATAEGMPSLIAGDFSATTVELVRSTPGFQPARRNPGGRAETPAASGGGSSGHGLDVLFQVKHFGGIRQQPILLPADGDLPGLRLGVMATLRLQGITATAE
>NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase
MAYTLPKLSYAYDALEPHIDAATMEIHHTKHHQTYINNVNAALEGTEYADLPVEELVKKLKSLPENLQGPVRNNGGGHANHSLFWTVMAPNAGGNPVGDVAKAIDKDLGGFDKFKDAFTKAALTRFGSGWAWLSVTPDKKVVVESTGNQDSPLMEGNTPILGLDVWEHAYYLKYQNRRPEYIGAFFNVIDWNEVERRYQEAIA
>NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease
MRNPRLLITAIALLLLGLVANHFLQRPPAPQFARDLQGTPVARAPATASPGKDSGLPAFLPAEARATIALIQRGGPFPHRQDGSTFGNREQQLPQRARGYYREYTVDTPGARTRGTRRIVTGGDPPEAWYYTDDHYESFRSFTVPAQGAQ
>NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor
MSHDDFGLGLHDINNAGVYAIDSDDIGALAAAMRDARLKVIRIDLEGVADKRTLLARLAAQLDFPAGFGGNWDALSDNLRDLQWLPANGYALFLADVDALRAGAHRDFDTLLDVMDETSRDWVGRDVPFWVFLSQSA
>NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein
MPLTRAEQLIDLLLARQQPRAVLEKSTRLPYGWALWLRSLGPLPRPFHAREVIAVFLPRPLPGPPGQSPWLSPWQALRRLFWQDWDAAPRDQRWMRWTSALVSALLHLLFFVLLLWVAVIRTTAPDEEGAEGERVQVEFVGRATQEGGGDQPGADVAAAAAAGRVATGQEAGAATAPAPRPVTAEAAASSPASAPTASVPPPPPAEAEPAPVAAPPPSPVQATEVAQASTDFVVPPVSVPRTEVSVVPRDSTPAVRERSVQPVQAPPAPSQVRIPELAVRTPQVRDIQVREREVSTVDAPVAPQPLRSAEMQVRVPQQDVQVREREVQAVVDPQVRMAAVAGREPAVRAPSGRDVQVREREVASAPVAAPASSSGSATSAPATAAQGSTAQASSSTRPSASSSTPASAGALPAPNPGNWATPAKGDDWGSSSRNRDGASSGARQASTTGKGTGLFNADGSVRVPGQEGDGHAERGAPGGANDGWSKERIAQSGTWLKRPPYDYTPTSFDKYWVPQESLLAEWVRKGVKAMEIPLPGTNSKISCVISILQAGGGCGLTNPNMQDQPAVARPPPDIPFKKELQEDNGSR

Crispr_ID: NZ_CP021768_8

• CRISPR_ID: NZ_CP021768_8
• CRISPR_location: 2937269-2937363
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_8

Consensus_repeat	Method
GCAACGGCAATGCGCAGCAGCAG	CRISPRCasFinder

spacers of NZ_CP021768_8

>8.1|2937292|49|NZ_CP021768|CRISPRCasFinder
AAGGATGGCGGCAACCGCAAGGAGCGCGGTGAGCAGCGCAAGGATGGCC

CRISPR arrays and Neighbor proteins around NZ_CP021768_8

CRISPR arrays

The CRISPR arrays of NZ_CP021768_8

>merge|NZ_CP021768|8|2937269-2937363|CRISPRCasFinder
GCAACGGCAATGCGCAGCAGCAGAAGGATGGCGGCAACCGCAAGGAGCGCGGTGAGCAGCGCAAGGATGGCCGCAACGGCAATGCCCAGCAGCAG

>NZ_CP021768|8|7|2937269-2937363|CRISPRCasFinder
GCAACGGCAATGCGCAGCAGCAG	AAGGATGGCGGCAACCGCAAGGAGCGCGGTGAGCAGCGCAAGGATGGCC
GCAACGGCAATGCCCAGCAGCAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_006377739.1|2932267_2932618_+|4a-hydroxytetrahydrobiopterin-dehydratase	unknown	unknown	gnl|CDD|234845
NZ_CP021768.1|WP_005410323.1|2943747_2944629_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP021768.1|WP_087923086.1|2939750_2942918_-|coagulation-factor-5/8-type-domain-containing-protein	unknown	unknown	gnl|CDD|366285
NZ_CP021768.1|WP_014037825.1|2952415_2952715_-|YciI-family-protein	unknown	unknown	gnl|CDD|183103
NZ_CP021768.1|WP_087923090.1|2952143_2952419_-|BolA-family-transcriptional-regulator	unknown	unknown	gnl|CDD|376601
NZ_CP021768.1|WP_087923089.1|2950957_2951995_-|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_CP021768.1|WP_014037813.1|2931577_2932177_-|NfuA-family-Fe-S-biogenesis-protein	unknown	unknown	gnl|CDD|132384
NZ_CP021768.1|WP_006456347.1|2942914_2943751_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP021768.1|WP_087923088.1|2947824_2950881_-|hypothetical-protein	unknown	unknown	gnl|CDD|224544
NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease	unknown	unknown	gnl|CDD|238340
NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor	unknown	unknown	gnl|CDD|240164
NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|377028
NZ_CP021768.1|WP_087923083.1|2934037_2935012_-|RluA-family-pseudouridine-synthase	unknown	unknown	gnl|CDD|182909
NZ_CP021768.1|WP_053443299.1|2945970_2947575_-|hypothetical-protein	unknown	unknown	gnl|CDD|227662
NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase	unknown	unknown	gnl|CDD|223678
NZ_CP021768.1|WP_087923087.1|2944625_2945966_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270450
NZ_CP021768.1|WP_008264832.1|2932614_2933031_+|energy-transducer-TonB	unknown	unknown	gnl|CDD|367555
NZ_CP021768.1|WP_087923085.1|2938863_2939748_-|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|377028
NZ_CP021768.1|WP_014037815.1|2933129_2933939_+|zinc-transporter-ZupT	unknown	unknown	gnl|CDD|235253

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_006377739.1|2932267_2932618_+|4a-hydroxytetrahydrobiopterin-dehydratase	gnl|CDD|234845	PRK00823, phhB, pterin-4-alpha-carbinolamine dehydratase; Validated.	3.85821e-44
NZ_CP021768.1|WP_005410323.1|2943747_2944629_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	7.30896e-90
NZ_CP021768.1|WP_087923086.1|2939750_2942918_-|coagulation-factor-5/8-type-domain-containing-protein	gnl|CDD|366285	pfam00754, F5_F8_type_C, F5/8 type C domain. This domain is also known as the discoidin (DS) domain family.	2.95865e-14
NZ_CP021768.1|WP_014037825.1|2952415_2952715_-|YciI-family-protein	gnl|CDD|183103	PRK11370, PRK11370, YciI family protein.	4.26702e-60
NZ_CP021768.1|WP_087923090.1|2952143_2952419_-|BolA-family-transcriptional-regulator	gnl|CDD|376601	pfam01722, BolA, BolA-like protein. This family consist of the morphoprotein BolA from E. coli and its various homologs. In E. coli over expression of this protein causes round morphology and may be involved in switching the cell between elongation and septation systems during cell division. The expression of BolA is growth rate regulated and is induced during the transition into the the stationary phase. BolA is also induced by stress during early stages of growth and may have a general role in stress response. It has also been suggested that BolA can induce the transcription of penicillin binding proteins 6 and 5.	4.95935e-34
NZ_CP021768.1|WP_087923089.1|2950957_2951995_-|LacI-family-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	5.2288e-110
NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	4.36479e-14
NZ_CP021768.1|WP_014037813.1|2931577_2932177_-|NfuA-family-Fe-S-biogenesis-protein	gnl|CDD|132384	TIGR03341, YhgI_GntY, IscR-regulated protein YhgI. IscR (TIGR02010) is an iron-sulfur cluster-binding transcriptional regulator (see Genome Property GenProp0138). Members of this protein family include YhgI, whose expression is under control of IscR, and show sequence similarity to IscA, a known protein of iron-sulfur cluster biosynthesis. These two lines of evidence strongly suggest a role as an iron-sulfur cluster biosynthesis protein. An older study designated this protein GntY and suggested a role for it and for the product of an adjacent gene, based on complementation studies, in gluconate utilization. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	5.21433e-72
NZ_CP021768.1|WP_006456347.1|2942914_2943751_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.04015e-87
NZ_CP021768.1|WP_087923088.1|2947824_2950881_-|hypothetical-protein	gnl|CDD|224544	COG1629, CirA, Outer membrane receptor proteins, mostly Fe transport [Inorganic ion transport and metabolism].	7.0764e-10
NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease	gnl|CDD|238340	cd00607, RNase_Sa, RNase_Sa. Ribonucleases first isolated from Streptomyces aureofaciens. In general, ribonucleases cleave phosphodiester bonds in RNA and are essential for both non-specific RNA degradation and for numerous forms of RNA processing. RNAse Sa is a guanylate specific endoribonuclease which belongs to the superfamily of microbial ribonucleases. Typical of this sub-family, the enzyme hydrolyses the phosphodiester bonds of RNA at the 3' oxygen end of guanosine residues to yield oligonucleotides with the guanosine-2',3'-cyclophosphate at the 3' end and the hydroxyl group at the 5' end. The terminal guanosine-2,3'-cyclophosphate is hydrolysed by guanyl RNAses to give guanosine-3'-phosphate.	8.67308e-43
NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor	gnl|CDD|240164	cd05141, Barstar_evA4336-like, Barstar_evA4336-like contains uncharacterized sequences similar to the uncharacterized, predicted RNAase inhibitor evA4336 found in Azoarcus sp. EvN1. This is a subfamily of the Barstar family of RNAase inhibitors. Barstar is an intracellular inhibitor of barnase, an extracellular ribonuclease of Bacillus amyloliquefaciens. Barstar binds tightly to the barnase active site and sterically blocks it thus inhibiting its potentially lethal RNase activity inside the cell. Barstar also binds and inhibits a ribonuclease called RNase Sa (produced by Streptomyces aureofaciens) which belongs to the same enzyme family as does barnase.	5.67799e-25
NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	2.51607e-08
NZ_CP021768.1|WP_087923083.1|2934037_2935012_-|RluA-family-pseudouridine-synthase	gnl|CDD|182909	PRK11025, PRK11025, 23S rRNA pseudouridine(955/2504/2580) synthase RluC.	3.98475e-112
NZ_CP021768.1|WP_053443299.1|2945970_2947575_-|hypothetical-protein	gnl|CDD|227662	COG5368, COG5368, Uncharacterized protein conserved in bacteria [Function unknown].	0
NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase	gnl|CDD|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	2.19761e-109
NZ_CP021768.1|WP_087923087.1|2944625_2945966_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270450	cd14747, PBP2_MalE, Maltose-binding protein MalE; possesses type 2 periplasmic binding fold. This group includes the periplasmic maltose-binding component of an ABC transport system from the phytopathogen Xanthomonas citri and its related bacterial proteins. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.04501e-138
NZ_CP021768.1|WP_008264832.1|2932614_2933031_+|energy-transducer-TonB	gnl|CDD|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	4.18892e-20
NZ_CP021768.1|WP_087923085.1|2938863_2939748_-|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	3.19248e-23
NZ_CP021768.1|WP_014037815.1|2933129_2933939_+|zinc-transporter-ZupT	gnl|CDD|235253	PRK04201, PRK04201, zinc transporter ZupT; Provisional.	1.31075e-130

Protein sequences

>NZ_CP021768.1|WP_087923083.1|2934037_2935012_-|RluA-family-pseudouridine-synthase
MTAQDPTKPAGDKPSVRMITVPADRAGQRLDNFLLGQLKGAPRSLVYKLVRSGQVRVNGGRAKAERKLEAGDEVRVPPVRLSEEGDKAAPPEAFMRRLEQAIVFEDARLLALNKPTGVASHGGSGISFGAIETLRALRPGQTLELVHRLDRDTSGLLIVAKKRSALSELQALLREDHGAGIRKRYLTLLAGRMPDGVMTVDAPLHVGLRQGGERHVQVNAIGKESISHFRVLERRGGHSYCEVRIETGRTHQIRVHAQHLGHPVAGDDKYGDPAVNKRLREQIGLKRLFLHAASLEFALDDGKSPYVLNAPLADELVEALDRLR
>NZ_CP021768.1|WP_014037815.1|2933129_2933939_+|zinc-transporter-ZupT
MLQIPPENIWIALAVTLAAGLATAIGSLLVLFSRRPNPRLLAFGLAFAGGAMVYVSLSEILNKSIASFALAYGERTGFTYGTLAFLLGVIVIVLIDHFIPNPHDSLDKQDPAFRENSREYLKRVALLTSIAITAHNFPEGLATFFATLESPSVGMPLAFAIAIHNIPEGIAIAVPVYFATQNKFYAFSASLLSGLAEPVGAALGYWLLSGSLSHATFGWVFGLIAGVMVFLALDELLPAAKRYAKGHETVYGLVAGMGTLAISLVLFKW
>NZ_CP021768.1|WP_008264832.1|2932614_2933031_+|energy-transducer-TonB
MNVRLLSLSLIAATGLAGCGASEPPAPPPPPPTEVAAVKTPPPQYPLELACMGVGGTSTFKVTIGTDGKPSEVALLTGAGNPQLDELAKTAVQGWQFNAATRNGQPVPATIQVPVSFNPPQPKPDQCFAIEERLRRGG
>NZ_CP021768.1|WP_006377739.1|2932267_2932618_+|4a-hydroxytetrahydrobiopterin-dehydratase
MADLIPLAQARCVPRKGSDHKLGEARLAELLPQVPGWELSEGGQALLRTFRFKNYYATMAFVNALAWIAHHEDHHPDLGVHYDRAVVRFSTHDVGGLSENDFICAAKTSALTEQLP
>NZ_CP021768.1|WP_014037813.1|2931577_2932177_-|NfuA-family-Fe-S-biogenesis-protein
MIQISDTAQTHFRKLIEREGVPGMGVRLSAVDPGTPRADARLEFAEPTDLLGDEWAVDCDGFTLYVDAGSVGWLDGAEIDIVAGTAGAQQLTIKAPRIKGEAPGDAASLVERVHWVVENEVNPQLASHGGKVAVQEVSSDGVVLLRFGGGCQGCGMADVTLKQGIEKTLMGRVPGVTAVRDATDHDSGHAPYIPRGNVA
>NZ_CP021768.1|WP_087923082.1|2929803_2931567_-|hypothetical-protein
MPLTRAEQLIDLLLARQQPRAVLEKSTRLPYGWALWLRSLGPLPRPFHAREVIAVFLPRPLPGPPGQSPWLSPWQALRRLFWQDWDAAPRDQRWMRWTSALVSALLHLLFFVLLLWVAVIRTTAPDEEGAEGERVQVEFVGRATQEGGGDQPGADVAAAAAAGRVATGQEAGAATAPAPRPVTAEAAASSPASAPTASVPPPPPAEAEPAPVAAPPPSPVQATEVAQASTDFVVPPVSVPRTEVSVVPRDSTPAVRERSVQPVQAPPAPSQVRIPELAVRTPQVRDIQVREREVSTVDAPVAPQPLRSAEMQVRVPQQDVQVREREVQAVVDPQVRMAAVAGREPAVRAPSGRDVQVREREVASAPVAAPASSSGSATSAPATAAQGSTAQASSSTRPSASSSTPASAGALPAPNPGNWATPAKGDDWGSSSRNRDGASSGARQASTTGKGTGLFNADGSVRVPGQEGDGHAERGAPGGANDGWSKERIAQSGTWLKRPPYDYTPTSFDKYWVPQESLLAEWVRKGVKAMEIPLPGTNSKISCVISILQAGGGCGLTNPNMQDQPAVARPPPDIPFKKELQEDNGSR
>NZ_CP021768.1|WP_087923081.1|2929224_2929638_+|barnase-inhibitor
MSHDDFGLGLHDINNAGVYAIDSDDIGALAAAMRDARLKVIRIDLEGVADKRTLLARLAAQLDFPAGFGGNWDALSDNLRDLQWLPANGYALFLADVDALRAGAHRDFDTLLDVMDETSRDWVGRDVPFWVFLSQSA
>NZ_CP021768.1|WP_087923080.1|2928772_2929225_+|ribonuclease
MRNPRLLITAIALLLLGLVANHFLQRPPAPQFARDLQGTPVARAPATASPGKDSGLPAFLPAEARATIALIQRGGPFPHRQDGSTFGNREQQLPQRARGYYREYTVDTPGARTRGTRRIVTGGDPPEAWYYTDDHYESFRSFTVPAQGAQ
>NZ_CP021768.1|WP_005410310.1|2927941_2928553_-|superoxide-dismutase
MAYTLPKLSYAYDALEPHIDAATMEIHHTKHHQTYINNVNAALEGTEYADLPVEELVKKLKSLPENLQGPVRNNGGGHANHSLFWTVMAPNAGGNPVGDVAKAIDKDLGGFDKFKDAFTKAALTRFGSGWAWLSVTPDKKVVVESTGNQDSPLMEGNTPILGLDVWEHAYYLKYQNRRPEYIGAFFNVIDWNEVERRYQEAIA
>NZ_CP021768.1|WP_087923079.1|2926917_2927766_+|endonuclease/exonuclease/phosphatase-family-protein
MRPLAHARLLLSCLLLLLALQAQARPQAPTAAASESEPRQLTVAALELPSRDDAQWKQRREQVAQLLTELQPDVISVQQVLQQQGRNPACWLASRLRYSCDFVTADPPSQPLRHGNAMLTRLPVSEDGVTLLHPPGTFSAAGMMRLKLGEALVNIYVARLRPDPDEATARQHQTSDLMTWIGATAEGMPSLIAGDFSATTVELVRSTPGFQPARRNPGGRAETPAASGGGSSGHGLDVLFQVKHFGGIRQQPILLPADGDLPGLRLGVMATLRLQGITATAE
>NZ_CP021768.1|WP_087923085.1|2938863_2939748_-|endonuclease/exonuclease/phosphatase-family-protein
MKQQGERVRATVRALGLAIALALPGAVMAAEPAAATAADVATAPGMSMVTFNLHHDREDWPSRRRTILAELKRLQPDAIALQEVIQRRNVRNQAQWLASQLGYKYVFVSTDPVGAPKRYGNALLTRRPILAQGDHLLLPLDDYRTVAHLRIDVDGTPVNVYATHLNERSDENGQRIRRAQVEDLLRFIATTSADAPVVIAGDFNALVDAGDLSELRSHYGDSYGSVHVNTDLAGVSTLNRHYYQAPSRIDHIFFQQDGMVAREAKLLFDQPDDNGRWASDHYGVWTRLQFAPAR
>NZ_CP021768.1|WP_087923086.1|2939750_2942918_-|coagulation-factor-5/8-type-domain-containing-protein
MKRAIAVGLGLLWTSLAIAAPPALPAPKVLDDFDDIGAWKLVLSDQVSGSLRPVSGAGGGRALCLDYDFHKVSGYVGIRRALNIDYPVNYRFGFQLRGDSPANDLQFKLIDASGDNVWWVNRPGYSFPKAWTPVEYRRRQIDKAWGPSPEKEMAGSAAVEFTIYSKVGGRGTVCFDKLTLQGLPPQDDSALVPSVIADTATALQDRMIDGKGDTFWISGGVKQQTISLDLHKSREIGGAVIDWLPNLEANRYTVRTSEDGRDWRTVREVTGGAGGRDWLALPDTDARYVRFDLLDGPNWRYGIRDITLKPLAFAATPNAFLSSVAADLPRGSLPRAYMGEQPYWTLLGLDGGQEQALISEDGALEPAKGSFSIEPFIRLDGKLLDWSKVAITQSLQDHYLPIANVDWVHEKAGLAVTSFVQGTPERAQLIGRYRLSNPDKVAHEYTLALAIRPWQVNPPTQFLNTVGGFSRIDALDVGEQLVRINGEPRIYPLQVPDARFASTFDGKLDAMHLASGKYPASTAVKDSTGMASGALLYTIKLEPGQSREVAVVLPQTGGWAPQALDVAKAQAQVAEQWRQKLGVVSLQVPAAGQALVDTLRTAVAHMLISRVGPRLQPGTRSYARSWIRDGAMISEGLLRMGRSDAVRDYINWYAPYQFENGKVPCCVDARGSDPVPENDSHGELIYSIAEYGRYTGDSTFAELMWPHVQGAYRYMEQLRASERTDENRARNPAFYGMMPASISHEGYSAKPMHSYWDNFWALRGYKDAASLAAQLGKVEAMQIAESRDQFRDDLQASLLSAMQQHNIDYLPGSAELGDFDATSTTIALAPGGEQGRLPQQALDATFERYWKEFVARRDGKREWKDYTPYEWRNVAAFVRLGWRDRAWQATEFFFKDRAPQAWNQWAEVVSRTPRKPFFVGDLPHAWVASDFVRSALDMFAYSRDMDDALVLAAGIPTAWLQGEGIAVQGLRTPQGQLNYRLQRSDKQLVLEVQPGLVPPVGGVVLPWPYVGDPGEATINGEAAEWVNKELHVHQLPARVEIDVPSAVRRAERKGQ
>NZ_CP021768.1|WP_006456347.1|2942914_2943751_-|carbohydrate-ABC-transporter-permease
MSREIGQSRWYPWMINGALLVLALVSLAPLLWMVSVSFMPQGEASHFPPPLLPSSITTHNYHELFARTGMGGNFANSLLVSLGITIGSLLLNTMAGYAFAKLNFVGRERLFQVLMAALVIPAQVAMLPLFLLMKQLGLVNSFGGVIVPALASVFGIFLVRQYARSIPDELLEAARIDGAGELRIFFQIVLPMLKPVLVTLAIFTFMGAWNDFMWPLIVLTDQEHYTLPVALATLSREHIMDVEMMMAGAVVTVVPVLALFLVLQRYYIQGLLLGSVKG
>NZ_CP021768.1|WP_005410323.1|2943747_2944629_-|sugar-ABC-transporter-permease
MKRTSLAGWIFAGPSLIVLGVFFGLPVASALALSVTDFDLYALADSSNLRFVGLGNYIDLLQTPMFWKSLWNTTYFVLIGVPLSIGVSLGAAMLLNAPAARFKALFRTALFAPVVTTLVAVAVIWRYLFHTSYGLVNYGLGHLGISPIDWLGDPNWAMPTIMLFAVWKNFGYNMVIFLAGLQAIPHDLYEAARIDGASRWKQFLHITLPMLGPVLLVVGVITVSGYFQLFAEPYVMTRGDPLQSTVSVLYFMFEEGFKWWNLGRASAVAFLLFLIILAVTTVMLRFGRKRQLV
>NZ_CP021768.1|WP_087923087.1|2944625_2945966_-|sugar-ABC-transporter-substrate-binding-protein
MPNWIDRLRRWALPALAALAVAGCARTEPGTTTVRFWAMGREAEVVSELIHEFEAENPGIKVDVQNIPWTAAHEKLLTAFAADGLPDVCQLGNTWVPEFAELDALTPLQPFVQRSTVVDPKDYFQGIWDTNVIHGELVGVPWYVDTRLIYYRKDLLAKAGYDHPPRTWQEWQEQMAAIKRMQGPNRYAVLMPINEFEQQLSLALQQPDPLLRDDDTRGNFASPGFRRTLAFYANMFEQGWAPKMSETQISNVWDEFFRGFNVFYISGPWNIREFKKLQPKELEGQWGTAALPGPDGLGAGIAGGTSLVIFRKSQQKEASWKLIEFLSRPEIQARFHSIIGDLPPRRSAWNAPSLANDPLAAAFRDQLERVRPTPKVLEWERIVQEMRIVTEKVVRGGLPQDKAVEELDQRVDKVLAKRRWMHEQQRLQERAPSPQSSSAVAAGSAQ
>NZ_CP021768.1|WP_053443299.1|2945970_2947575_-|hypothetical-protein
MQARHLLSAAALSLAVAACQPAQQEPAKPRPPVILIEADAPPRPMKPVLPPLFDDIERRTFQFFWDTTNEINGLTPDRYPSRPFASIASVGFALTAYPIGIENGWVSRNQAIDRTLTTLKFFRDVPMGPQRTGKAGYKGFYYHFLDMQEGRRYDSWVELSSVDTALLMMGVLFAQSYYDGDDPREKEIRQIADTLYKKVDWPWLQQRAPLISMGWFPESGFIDHDWMGYNEAMMVYILALGSPTHPVSPDAWTVWTRTYDNDWGVYQGQEYLSFGPLFGHQYSHVWIDFRDIQDAYMRERGSTYFLNSRSAALAQREYAIANPMQWKEYGENVWGLTASDGPQNTTQEYRGEQRQFRHYSSRGAGLRENFDDGTIAPTAAIASVVFAPEQVIPATLEMHKRFGDYIYSSYGFLDSFNPSFNYDIPIKTGRLVPDRGWVASDYIAIDQGPILTMIANYRDDFVWEVMKKNPYIRKGLERAGFSGGWLAPEGSFQPLELQKDEKAAAARAVGIAESRAAAAQEQKNNANRTTGQGK
>NZ_CP021768.1|WP_087923088.1|2947824_2950881_-|hypothetical-protein
MMHTTFRTPARRLLSTALVSCLMLAAAPNVMAQSANASLRGQVAGAQAGTEVTATNVATGTVRRGTIRADGSYSLMGLDPGTYDVVANGQTQKVTVTVASTATLNFAGAASSTPGSTAATNLDTVNVVAPTLLQEVRTSEVGKTVSLQQIQTTPQVSRNFLEFADAVPGLIFTRDAKGNTSLRGGATNADGTNVYIDGVGQKSYVKGGGVAGQSGSAGNPFPQLAIGEYKVISGNYKAEYGQVSSAAVTAATKSGTNEFKGEAFYRYTDEDMRAKTPAERQGGKDKMVSAEKEYGFALGGPIIQDKAHFFVTYEAKRFDLPVTIAPDGAVTGAAGLLPPAGAAGLGPASQPFQQDLIFGKIDFEPTDNDRIELTFQDRDETQSQFSGQTSPEAGREVVNTDRRYALRWNHSGERYYNELMLTHEDSFNNPNPLTLANGITYTAPDGPEDRTVVKIGGASALDSQVKGQKGWSIEDNLTLDGIRWAGDHTIKMGVKYKQIDLYASDAAQINPTFTYSLGDPDFPDSIPYKAQFVKPVTGVSGVSGEVRSKSKQYGVFIQDDWQVNDHLQLNIGLRWDYEKTPSYLDFVTPQQVVDAIYSQDPRAPAGQTYADSLALGGLDIGDYISNGHNRKAFKDAWQPRLGFSYDINADEQHVIHGGAGRSYDRDLFDNLQLETTKLALPQPTIYFRNPATGACINGQAACYDWNPNLLNGIGNLQSLVGATSNAGLEVDLLNNKLKAPYSDQFSLGMSNQIGDWLTDATIARTLSYDGFAFTLGNRYPTGQFFDDPRLCGGTDPGLSQAWSCNVPGFGSLIIGQQGIKTRATQVLLSAQKPFTKESGWGTSIAYTWTTARHNRDINEKYAFDRGLIGDYPTIRSNGAPRHRLVVTGSYAGFWGITFGGKITLATPTAVNDWYPVMQASGYTLPTPQAAVPNATGKFLVGGKIFGYRSVDLQATKTFKMPGDTELYARIDIINVFNFDNFSTYNYVKTNGKLQASYNETGEIIGTPRQIKAEVGFRF
>NZ_CP021768.1|WP_087923089.1|2950957_2951995_-|LacI-family-transcriptional-regulator
MEGGFVNKAAITIKDVAREARVSVATVSRALNGHENVAEPVRQLVLEVAARLRYTPHAAARSLSSRRTNTVGVVLPDLYGEFFSELMRGIDGVARSRRQHLLVSSYHGDQEQQGAALRAMRGRVDGLLVLSPYAESPGFLTDNLPQSLPTVLINTYLPGQDHPVLSIDDHAGAMAMTRHLLDAGHRRIAFISGPDLNFDARERLRGFRDALVAFGSGAEGIELPGDFDEASGHRAGQELLAAGALPDAVFAANDMMALGCLYAFTQAGVRVPADVALAGFDDIPLARFVHPSLTTMQVSIAELGDRAMTRLLQLMDGTSTDGTGDKQTLVPRLIVRDSTTPPSGR
>NZ_CP021768.1|WP_087923090.1|2952143_2952419_-|BolA-family-transcriptional-regulator
MNAERIGRIRDALQQALAPSVLEIEDDSHRHAGHAGARDGRGHFNVHVVSERFAGLAPLARHRAVYAALGSMMDTDIHALSIRAQTPSEQG
>NZ_CP021768.1|WP_014037825.1|2952415_2952715_-|YciI-family-protein
MWYVIEGYDGQDVLAQRLQARPEHLARLHALRDEGRLLLAGPCPAVDSEDPGPAGFSGSVVIAQFESLPQAQAWADADPYVAAGVYTRVQVRPFRKVLP

Crispr_ID: NZ_CP021768_9

• CRISPR_ID: NZ_CP021768_9
• CRISPR_location: 3170193-3170297
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_9

Consensus_repeat	Method
GGCGGATGCTCCGTGATGCGTGCATGCCGCGCCCATGC	CRISPRCasFinder

spacers of NZ_CP021768_9

>9.1|3170231|29|NZ_CP021768|CRISPRCasFinder
CACACACCCGGTAGCGCCGGGCCATGCCC

CRISPR arrays and Neighbor proteins around NZ_CP021768_9

CRISPR arrays

The CRISPR arrays of NZ_CP021768_9

>merge|NZ_CP021768|9|3170193-3170297|CRISPRCasFinder
GGCGGATGCTCCGTGATGCGTGCATGCCGCGCCCATGCCACACACCCGGTAGCGCCGGGCCATGCCCGGCGGATGCGCCGTGATGCGTGCATGCCGCGCCCATGC

>NZ_CP021768|9|8|3170193-3170297|CRISPRCasFinder
GGCGGATGCTCCGTGATGCGTGCATGCCGCGCCCATGC	CACACACCCGGTAGCGCCGGGCCATGCCC
GGCGGATGCGCCGTGATGCGTGCATGCCGCGCCCATGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087923233.1|3179490_3180735_-|DUF418-domain-containing-protein	unknown	unknown	gnl|CDD|225193
NZ_CP021768.1|WP_087923228.1|3170347_3172354_+|M13-family-metallopeptidase	unknown	unknown	gnl|CDD|341056
NZ_CP021768.1|WP_005410509.1|3174698_3175373_-|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|223777
NZ_CP021768.1|WP_014647924.1|3180834_3181317_-|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223976
NZ_CP021768.1|WP_087924207.1|3175801_3176722_-|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP021768.1|WP_087923223.1|3153930_3156990_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP021768.1|WP_075075896.1|3175466_3175775_-|cysteine-methyltransferase	unknown	unknown	gnl|CDD|226219
NZ_CP021768.1|WP_087923232.1|3178236_3179487_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|234819
NZ_CP021768.1|WP_087923231.1|3176881_3178240_-|glutathione-disulfide-reductase	unknown	unknown	gnl|CDD|235701
NZ_CP021768.1|WP_087923225.1|3161333_3164141_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP021768.1|WP_042359268.1|3157062_3157917_-|iron-sulfur-cluster-carrier-protein-ApbC	unknown	unknown	gnl|CDD|378455
NZ_CP021768.1|WP_087923224.1|3158131_3160921_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP021768.1|WP_087923227.1|3167937_3170040_+|peptidase	unknown	unknown	gnl|CDD|226118
NZ_CP021768.1|WP_087923229.1|3172478_3172961_+|VOC-family-protein	unknown	unknown	gnl|CDD|226383
NZ_CP021768.1|WP_087923222.1|3152936_3153509_-|dCTP-deaminase	unknown	unknown	gnl|CDD|234753
NZ_CP021768.1|WP_014037994.1|3152232_3152655_+|HIT-family-protein	unknown	unknown	gnl|CDD|223611
NZ_CP021768.1|WP_087923221.1|3151564_3152236_+|dienelactone-hydrolase-family-protein	unknown	unknown	gnl|CDD|223489
NZ_CP021768.1|WP_087923226.1|3164262_3167379_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|369481
NZ_CP021768.1|WP_014037992.1|3150740_3151199_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087923230.1|3172957_3174544_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224154

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087923228.1|3170347_3172354_+|M13-family-metallopeptidase	gnl|CDD|341056	cd08662, M13, Peptidase family M13 includes neprilysin and endothelin-converting enzyme I. The M13 family of metallopeptidases includes neprilysin (neutral endopeptidase, NEP, enkephalinase, CD10, CALLA, EC 3.4.24.11), endothelin-converting enzyme I (ECE-1, EC 3.4.24.71), erythrocyte surface antigen KELL (ECE-3), phosphate-regulating gene on the X chromosome (PHEX), soluble secreted endopeptidase (SEP), and damage-induced neuronal endopeptidase (DINE)/X-converting enzyme (XCE). Proteins in this family fulfill a broad range of physiological roles due to the greater variation in the active site's S2' subsite allowing substrate specificity. NEP is expressed in a variety of tissues including kidney and brain, and is involved in many physiological and pathological processes, including blood pressure and inflammatory response. It degrades a wide array of substrates such as substance P, enkephalins, cholecystokinin, neurotensin and somatostatin. It is an important enzyme in the regulation of amyloid-beta (Abeta) protein that forms amyloid plaques that are associated with Alzeimers disease (AD). ECE-1 catalyzes the final rate-limiting step in the biosynthesis of endothelins via post-translational conversion of the biologically inactive big endothelins. Like NEP, it also hydrolyzes bradykinin, substance P, neurotensin, and Abeta. Endothelin-1 overproduction has been implicated in various diseases including stroke, asthma, hypertension, and cardiac and renal failure. Kell is a homolog of NEP and constitutes a major antigen on human erythrocytes; it preferentially cleaves big endothelin-3 to produce bioactive endothelin-3, but is also known to cleave substance P and neurokinin A. PHEX forms a complex interaction with fibroblast growth factor 23 (FGF23) and matrix extracellular phosphoglycoprotein, causing bone mineralization. A loss-of-function mutation in PHEX disrupts this interaction leading to hypophosphatemic rickets; X-linked hypophosphatemic (XLH) rickets is the most common form of metabolic rickets. ECEL1 is a brain metalloprotease which plays a critical role in the nervous regulation of the respiratory system, while DINE is abundantly expressed in the hypothalamus and its expression responds to nerve injury. A majority of these M13 proteases are prime therapeutic targets for selective inhibition.	1.10501e-169
NZ_CP021768.1|WP_005410509.1|3174698_3175373_-|rhomboid-family-intramembrane-serine-protease	gnl|CDD|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	6.36451e-38
NZ_CP021768.1|WP_014647924.1|3180834_3181317_-|peptidylprolyl-isomerase	gnl|CDD|223976	COG1047, SlpA, FKBP-type peptidyl-prolyl cis-trans isomerases 2 [Posttranslational modification, protein turnover, chaperones].	3.66751e-54
NZ_CP021768.1|WP_087924207.1|3175801_3176722_-|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].	5.16659e-10
NZ_CP021768.1|WP_087923223.1|3153930_3156990_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	2.23768e-10
NZ_CP021768.1|WP_075075896.1|3175466_3175775_-|cysteine-methyltransferase	gnl|CDD|226219	COG3695, COG3695, Predicted methylated DNA-protein cysteine methyltransferase [DNA replication, recombination, and repair].	6.83499e-21
NZ_CP021768.1|WP_087923232.1|3178236_3179487_-|FAD-dependent-oxidoreductase	gnl|CDD|234819	PRK00711, PRK00711, D-amino acid dehydrogenase.	2.78967e-76
NZ_CP021768.1|WP_087923226.1|3164262_3167379_-|TonB-dependent-receptor	gnl|CDD|369481	pfam07715, Plug, TonB-dependent Receptor Plug Domain. The Plug domain has been shown to be an independently folding subunit of the TonB-dependent receptors. It acts as the channel gate, blocking the pore until the channel is bound by ligand. At this point it under goes conformational changes opens the channel.	1.64432e-16
NZ_CP021768.1|WP_087923231.1|3176881_3178240_-|glutathione-disulfide-reductase	gnl|CDD|235701	PRK06116, PRK06116, glutathione reductase; Validated.	0
NZ_CP021768.1|WP_087923225.1|3161333_3164141_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	9.35557e-29
NZ_CP021768.1|WP_042359268.1|3157062_3157917_-|iron-sulfur-cluster-carrier-protein-ApbC	gnl|CDD|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	1.8127e-146
NZ_CP021768.1|WP_087923224.1|3158131_3160921_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	6.60575e-20
NZ_CP021768.1|WP_087923233.1|3179490_3180735_-|DUF418-domain-containing-protein	gnl|CDD|225193	COG2311, COG2311, Predicted membrane protein [Function unknown].	2.74559e-86
NZ_CP021768.1|WP_087923222.1|3152936_3153509_-|dCTP-deaminase	gnl|CDD|234753	PRK00416, dcd, deoxycytidine triphosphate deaminase; Reviewed.	3.60975e-109
NZ_CP021768.1|WP_014037994.1|3152232_3152655_+|HIT-family-protein	gnl|CDD|223611	COG0537, Hit, Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases [Nucleotide transport and metabolism / Carbohydrate transport and metabolism / General function prediction only].	1.49308e-16
NZ_CP021768.1|WP_087923221.1|3151564_3152236_+|dienelactone-hydrolase-family-protein	gnl|CDD|223489	COG0412, COG0412, Dienelactone hydrolase and related enzymes [Secondary metabolites biosynthesis, transport, and catabolism].	4.70313e-38
NZ_CP021768.1|WP_087923229.1|3172478_3172961_+|VOC-family-protein	gnl|CDD|226383	COG3865, COG3865, Uncharacterized protein conserved in bacteria [Function unknown].	3.24993e-73
NZ_CP021768.1|WP_087923227.1|3167937_3170040_+|peptidase	gnl|CDD|226118	COG3590, PepO, Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP021768.1|WP_087923230.1|3172957_3174544_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224154	COG1233, COG1233, Phytoene dehydrogenase and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	5.02915e-106

Protein sequences

>NZ_CP021768.1|WP_087923227.1|3167937_3170040_+|peptidase
MTRTPKIVLLTLAVSAALVGCGKTETPAKDATASAPATAEATTYKLDDSKLPAYNAFQPSDLDTTKDACTAFGDYVNSKWLAANEIPGDRTSWGAFTILDERSVAVQHQLAEQVAQVKTPNHIEKIVGDLWATGMDEAKINAQGIEPLKADLTAIDGLQDKAAIADYLRSSAAKGDNVLFGFGAEADFKNSAMNMAYASQGGLGLPDTTYYTDAKNADKLKAYQAHVAKVLELSGVAAADAAKQAEDVVKFETRLAKASKSRVELSRNVELYYNPVTLADADKLTPNFSWTEFFKSQGVAAPEKFSLAMPAFHEEVSKALADTDPSVWRAYLRFHTVDSASPYLADAFVQENYEFYGKTLNGQKEQKPRWKRVLGTIENDAGEAFGQLYVKVAFSPEAKAKMEELVKNLAASLKDRIQGLSWMSEETKAKAIAKWETFTPKIGYPDKWRDWSGLQTQRDSYLGNVRAANEFNYKFNLSKIGKPVDKTEWGMTPQTVNAYYNPLQNEIVFPAAILQPPFFDPKADDALNYGGIGAVIGHEMTHGYDDQGARFGPTGNMEDWWTPADKKNFEGLTGKLVKQFDQYKVDGQAVNGHLTLGENIADLGGLATAYDALQKATAGKEDAKVDGFTRDQRFFFNWATVWRTKYTPENAKVRLATDPHAPAQFRAMGAPSNLPTFAAAFQCKAGSPMARAGEQQVVIW
>NZ_CP021768.1|WP_087923226.1|3164262_3167379_-|TonB-dependent-receptor
MEKTRPLHRNPLSLALSSALLLAAALPAFAQEGEAAKDTAESAKKASNEAAATQLDRITVTGSHIYRAGYDTLEPAAVVSRQDIEAYGHTNLIDALTKIPGVSAGVSSRGDQAGFGAGVNFASRFGLGSNRLLTLVNGRRFVTSAPPTVFGAGGGSGIQVDMNAIPTVMVERVESLSIGGAPTYGSDAISGVNNIILRDKFEGAEVEIGFGRTTKNDNDRYSWSAIFGSGFADGRGHFTIAAELDNSDGVNALQRDFYRNGYSLQTNPTAANVARFQSWRTPGNDGRIDPGIPFNTGPADGIADQVWIRNRRISSMTFGGLIMPSDIQVRRSYQRNATGELNGFGPNNKLWHFNNKGDLVAYDPGISYPSGNASGGDGLNLNETLPLIADLERRTVYSTGSFDFNDNVRGFFELSHYSATARETLDQNVYNAAGFGAANPDGSGDQSGAMLFSANNPFLSAESRRILAENGITSFRLSRSSRDLSMNNASTDTRLSRIVLGLDGFFDIGERRFNWETSVTHGRGDFDYKGTGLIQQNFINALNVKRDASGNIVCDASAPGTTADPNCRPLNLFGENQASPEALAYVSTPTLAKARTRQTVFNASVTGGLFDLPGGEFSFAAGVEHRREEGSFTPSEYQRLGQGRSVPIQGAKGDYHTNEIFAEFLAPLFNPDWDLPGLHRLDVTLKGRRVVNSVAGGFNAYTYGVQYEPFAGIQLRGSKTQSLRAPSIAELYTSLQPAYYNIPEVCSVSAINGGTNPAIRRRNCEAFFQAYPGADPATFQASPTNTLGSVNGYTGLKNEKAKSWTAGIVFAPDWAKGLRVAADWYDIKITDVITSLSPTDIITGCFDNPDFNASNVPNANRFCSLVTRNPLSGAATDIRTEYGNGPVLMFRGWTAEVDYNWDMGRFGQVALGFYGYMPKNRGQAANTDVPFVERVGTFDEPKRQFRWTAQHAIGKWSYGVTSNYTSGSQFSLTATPESRQYFKRDSWTTWDANVSYRLTDNARVNLSVLNLSDDIGPFPYVLDALGRRYMASLRYSFR
>NZ_CP021768.1|WP_087923225.1|3161333_3164141_+|TonB-dependent-receptor
MSRQRSTLSRHPLTLALMGTLLASGTALAQDGNAPTQLDRVTVTGSLIPQTEIENHTPVLTVTAEDIQTRGFTSVADVLQQSSLSTGGLQGGQTSASFTQGAEAAGMFGLSPGYTKYLINGRPMLSYPALYNGGDTFNNISGIPIDIVERIEILPGGQSSLYGSDAIAGVVNIILKERMDGGVLNVRGGAYSEGGGNSFRLSGARGFNSKDDRFHALVNVQYEKTSPIWGYQRDLTKVNNPDGYSPQYVSNDFLVLLPAANNRYAMMDPNLCANVAGQFDGTTVLGTRPTGQACGSVYGTGYKTIKNGKESGQIYSSATFDVNDNFQLFGDALYSLEEVKYATGSGYTWWGTSSGWGRFYDQTSGQYMNLQRVFAPEDIGGGGYRDIMNTDRNKAYQVTLGGRGTAGNWDYSLSFTRGEYKLTERNFVRWNDPINDYFEQRVLGPVLGTTSTGYDIYSPNWEAFYAPLPAGDFQSFTGYSYSESRTWQNLARAQVTNGSLFKLPGGDAGFAVVVEGGSEGWDYTPDPGLMDGSVWGTTAVSGAGHRSNYAVTTELRMPLLETLTVTGSGRYDAFKIGSNTVDKATYSVGIEFRPIDSLLFRGKYGTAFRAPTLSDAFQGRSGYYANGSTDYYRCGQLGFDPANTTGCPYDSVSVFGTRSGNPDLEPITADVWNAGVVWAPINNLSLSVDYYNWKIKNEVDTLSSDQLLLAEYYCRNGQSNNTSASCQNVNDWITRDASGVLDEIYTPKMNVARQNLEALTASFKYVQDIGRFGSLQFSANYTDMLKRKLQPQPGDEYLDLLRDPYAMWVYDSYAKVRADGSIGWAKDNWTTTLYANYIGKTPNYMAYVGNGYDYVHSSGYKAGKWGSYTTYNLSVNYRAMENLTLSLMVNNVFNKMPDNQRYSFAGTSGQPYNNYLYNAYGRAIYVQAKYAFGVK
>NZ_CP021768.1|WP_087923224.1|3158131_3160921_+|TonB-dependent-receptor
MKHVSNTARRNTLAVALISALMAAAPAMAQDKATNLDKITVTGSLIPQTQVETQTPVMSITAEDIQTRGFSSVAEVLQQSSLTTGGLQGGQTSGAFTQGAEAAGMFGLNPGYTKYLINGRPMLSYPALYNGSESFNNISGIPIDIVERIEVLPGGQSSLYGSDAIAGVVNIILKERMDGGTMSIRGGTYTEGGGSNIRFSAAKGFNAFDDRFHALVNVQIENGSPIWGYQRDITKQNNPVGYTAQLPSNDFAVIGNADNKLYMMDPTRCANVAGLYDGTTTVGKRASGESCGSVYSAGYKTLKNGKNSGQFYSSMTFDVNDNFQLFADVLYSKEKTEFTSGSSALWWGTKSVMGGFYDQGLGKVVNLQRAFAPEEIGPGHYNNILNSDESRSYQVTLGGKGMVGDWDYSASFTRGEYRLDQNRFARWKDKIEGFFGETVLGPRLGTTADGFGIYNPDYTAFYSPITPDQFASFTGYGTHRSKTWQNLGRVQVTNGSLFSLPGGDAGLAVVLEGGSEGWDYSPDQAFVDGNAWGASAVAGAGHRSNYAVTSELRMPVFESLTISASGRYDAFKIADKTVDKATYSIGLEYRPVESLLLRGKYGTAFRAPTLSDAFQGMSGSFASGQNDYYRCSQMGYALRDEACSFYKTTSVYSEKSGNPDLKPITADVWSAGVVWAPVSNFSLSVDYYNWKIKNEVKTLSTDQLLLAEYQCHNGLPNNTSASCQNVTDWVTRDAGGNLTRVYTPKLNVASQNLEAVTVGAKYQQDLGRFGSLMFSGNYTNMLKREVVALPGAQKLDLLSDPYNMWYYDNFAKVRGDVSVGWAISKFTTTVYANYVGSTPNYLAYTGRSYDYVHSSGAKAGKWGSYTTYNMSLNYQAQDDLTLSLMVNNVFNKLPEGQRYNYPGNESTPFNDGFYSVYGRQISAQVKYDF
>NZ_CP021768.1|WP_042359268.1|3157062_3157917_-|iron-sulfur-cluster-carrier-protein-ApbC
MNSSPRRPHVSQVQKGLTPHARIRNVIAVGSGKGGVGKSTTSVNLAVALQQLGARVGVLDADIYGPSVPAMLGLSGRPESPDNKSIEPLRAFGVDTMSIGYLIEEDTPMIWRGPMATSAMTQLFNDTLWDDLDFLLIDLPPGTGDIQLTLTQKIPLAGAVIVTTPQDIATLDAKKALKMFEKVEVPVLGIVENMAVHTCSSCGHIEHLFGEGGGERMAAQYGVPLLGSLPLQIGIREQGDAGTPITVAQPDSAPAQAYRHAAQRLIEEVGKRPRASIPILSSLL
>NZ_CP021768.1|WP_087923223.1|3153930_3156990_+|TonB-dependent-receptor
MNLNFNGRTLKRTALALVLGALAGTSYAQSTTGDIVGSVTSADKIQVKSLASGTTREVNVSSDGRFRVSQLPTGTYEVSTVSNGSPTATTRVTVVAGQSSMATFASASSGSATSLETVNVRALGAANAIDLGSVESRTTFTADKLNSLPVARDVTSVSLLTPGTVSSSGYFGPASFGGASAAENSYYVNGFNVTNLYDSLSFSEIPYQAIDQLDVQTGGYGAKYGFSTGGVTSVNVKRGTNEWKGGFSWTGAPDSLRENEPDTYYNDGSIFRSYDKNSSSSNVYSVWAGGPLIEDKLFVFAMGQFSNSKTGSYSNRGSQYTTNGRPPSAAALSTTGYDYESKTPYWLLKVDWYLNENNHLEYTGFDNSRRYSYNYFNALYDKPDAAGEPARTNDLGELIGKTGGQTDIFKWTSYLTENLTGSIQYGQMRNRSSEHTISPDGVTSFYDGNINSPEGACPYVLDYRSETGGTGRRIGCAVASTVGMFGGRNERKGARADFDWQLGDHKIGFGYSDEKWTSVQGTSYSAGALWYLEDDYANRVNFRNGGSIEIKQKSWYVQDNWQITNNFMLYAGIRNDSFDNKNSDGISFVKQDDIWQPRFGFSWDILGDGRSKLFASAGRYSLPIAANVALRAASASYYLDQYFTYDGINPNGSPIITGSYEDGAYDNIVNGESGVTPDPRAVASKGLKPYTQDEVILGYQQQINSSIDFFNDWTVGIKATYRRANKVIDDTCDSRSLYNAAVAAGYDLSNWADPWTVPEGLPGCWIYNPGSDLQVTLDVDGDGNVDDITVPGASLGPKAKRVYKAVTLSADKQTERWYASFSYTWSKLEGNYEGLVKSTNGQDDTGTTSDFDFAEIMYGSDGYLFNDHRHSIKLYGGFRFTDEWSVGVNMLAQSGAPKSCLGGGWGSFDTEYGYSGVFHSCELNGNQPADDISKVGSAGRTPWQFTVSPNITYTPNWLKGLSVQMSVINAFNNIKPVQVYETKYGRPSSAPTIRTYYNYNTPKYFNDPRYVRFQVQYDW
>NZ_CP021768.1|WP_087923222.1|3152936_3153509_-|dCTP-deaminase
MSIKSDRWIRRMSEQHGMIEPFEAGQVKQANGQRIVSYGTSSYGYDVRCSREFKVFTNINSTIVDPKHFDSGSFVDITADECIIPPNSFALARTVEYFRIPRDTLVVCLGKSTYARCGIIVNVTPLEPEWEGHVTLEFSNTTPLPARIYANEGVAQMLFFQAAADDICETSYRDRGGKYQGQTGVTLPRT
>NZ_CP021768.1|WP_014037994.1|3152232_3152655_+|HIT-family-protein
MSEFELDSRLATDSVLVAEGPLSQVRLMNDERFPWLVLVPRLAGVTEWIELDGEQQDKLRTELNRACKALKGSDGVEKINIGALGNIVRQLHFHVIGRHDGDPAWPGPVWGSGPAHRYEPAALDQHVAYWKERLGYPAQS
>NZ_CP021768.1|WP_087923221.1|3151564_3152236_+|dienelactone-hydrolase-family-protein
MAEWITLDTHHGPVRAWQALPEGTARGGLVVVQEIFGANPHIRSVAERFAAEGYAVLAPSFFDLVDGPDADPDALPYDAEGVKQGLERVGALGMERALEVVRAAATRLAPQGKVGTVGYCWGGTVAMLSAVRLGLPSVSYYGARNVQFLDEVPKAPVIFHLGAQDRSIPPEAVQAHREKLPQMATYVYPADHAFNREVGHAYDPDSAALALQRTLDFFSEHLG
>NZ_CP021768.1|WP_014037992.1|3150740_3151199_-|hypothetical-protein
MSINQAISAQDSALYVKAGTAPTAPNNPAGYTEIDGLTAFPFGRGQANTLDATNLRSKQMENIAGLSGGQAVQVSGHRWPVGSSAGQEILRDADPDADLHFLMVLPTGDAATFVAKVAAFNVAPGTNQVLTFTADLLPREFALVTVAAGGTP
>NZ_CP021768.1|WP_087923228.1|3170347_3172354_+|M13-family-metallopeptidase
MPNFRPLAIALGISLATLVPTHDAFAAKKKAARAPAVSAQCSDFYGATNAGWLKANPTPQIGATTALGQLVDRSRQQQRELLDAAMKSPQGNVQKLLGDFWASGLDEAAVEADGSNPIAPLLTRINAIKKAKDVPASIAALHQVGIPVAFNFGPDVDLKALDRHIGYFMQGGMGLPDPAFYTRTDADTVALMGRYRNYVKQILALTGTPAAKLDAESQSVIALETELARNAQSLAGINNPFNNYAPISTKELNSRYRNLQLDAFLKAQGVDDDLVSLADPGLFKQLDGMVTKLKPDQWKAYLRWRVGDAMAPYLSKAYRDAEFEFRGRVLRGETLPPQRWEDVLDAINVAAGPMVGREYAARYLSAEDRRQAAWIVDKLREVQIEAVKNNSWMSAEAKTEAQAKLAALKIEIGTPLRDLDYSVQPMGRGSFGGNMLIASTWRHREEMKRIGKGNADRRWDVLPQQPSLAYDLAQNRLIVTAAILQGPVFNAKADAADKFGSFGGLVGHELTRAIDAKGALVDAKGELRSWWTPADKTAWTLLGNRVAAQYSAYDFPGVKGAKVNGTLTQEENLADIAGLELAWAAYTAQEPKAKQAQQQGFFRAWSTLWAQQLSPNEAVRRLTADIRAPGLWRSNGTLANLPAFGATFSCKAGQPMQRSEADQIKVWR
>NZ_CP021768.1|WP_087923229.1|3172478_3172961_+|VOC-family-protein
MAHKNTICVWYDNGALEAATFYASILPDSAVTAVHHAPGDYPDGREGNVLTVEFTVCGIPCVGLNGGTAFKHSEAFSFQIQTEDQAETDRLWDAIVGNGGQESQCGWCKDRWGISWQISPRMLIEAVTSKDKALAKRAFNAMMPMKKIDIATIEAAIRNA
>NZ_CP021768.1|WP_087923230.1|3172957_3174544_+|NAD(P)/FAD-dependent-oxidoreductase
MTTWDAILIGGGHNGLVCAAYLARAGKKVLVLERRGVLGGAAVTEEFHPGFRNSVASYTVSLLQPKVIDDLQLHAHGLRIVARPANNFLPLPDGRYLLSAPGRTQAEVAKFSERDAQRLPAYEARLEIFADVLRAWALRTPPDLGAAGGWRALPALWQMGRLGRELATLDASLRQELLDLFTLSAAEYLDRWFESEPIKALFGFDGIVGNYASPYTPGSAYVLLHHVFGQCNGVKGAWGHAIGGMGAISQAIAASAREAGAELHVEAGVQRVRIEQGRAVGVELANGEILRARAVIANVNPKLLYEQLLEPEQVPNATRERMANWRCGSGTFRMNVALSRLPDFSALPGSGDHLGAGIIMAPSLDYMDRAWLDARRDGWSREPIVEMLIPSTLDDSLAPPGQHVASLFCQHVAPVLPEGRHWDDHRETVADLMIATVERHAPGFTASVLGRQVLSPLDLERTFGLVGGDIFHGALSANQLFSARPMVGQAGYRGALPGLYLCGSGTHPGGGVTGAPGHNAAQVVLRDL
>NZ_CP021768.1|WP_005410509.1|3174698_3175373_-|rhomboid-family-intramembrane-serine-protease
MFPRLPTVTKALLIANAILFLLQQPFLLGMQTFEPFMLQPLQQGFDAFSPGGNFQPWQLLTYGFLHGSFGHLFFNMLAVFMFGAPLEQTWGEKRFLLYYLVCVAGAGVCQLLVGTLLENPATVLGASGGVFGLLLAYGMLFPNQRVMLLFPPIPMKARTFVILFGVGELVLGMTGWQPGVAHFAHLGGMLFGWLLIRYWRGQPPFNKRRPPGPPKRPNHLRSVK
>NZ_CP021768.1|WP_075075896.1|3175466_3175775_-|cysteine-methyltransferase
MAVIRAIPAGQVMGYGQVAMRAGLPGRARLTARILGQNDDPDLPWHRVLRSDGRIAMEEGSAGWREQSQRLRAEGVRVENGRVRMPATDPAAALDAAVWGPG
>NZ_CP021768.1|WP_087924207.1|3175801_3176722_-|DMT-family-transporter
MSNTASRIATASPRIALGGIGLAAIGAIAASGKAIIVKLGLRHGVDATTLLALRMLMALPLFALMAVWAARRAEPLSWADRARVLWLGFTGYYLSSLLDFQGLQYISVTLERLILYLNPTLVLLINVLLARQRPGRWQIGALVLSYLGVLLAFGHDLQREGGQIIVGSLLVLGSALSYALYLFGSGQVVARIGAVRLTAYASCVAGVLVLLHFAVTHPLPLLWQAPAPVQWLSLVNATVCTVLPVLAIMLAVQRVGSSLAAQVGMLGPVSTIVMSLWLLDEPMGPAQIAGTVLVLIGVLLVTRLRR
>NZ_CP021768.1|WP_087923231.1|3176881_3178240_-|glutathione-disulfide-reductase
MSTASYDYDLIVLGGGSAGLAGAIRAAQHGKRVAMLEPGELGGTCVNVGCVPKKAMWLAADLHERIGLASAMGFEVEARPALSWKELVIHRQAYISNIHTSYHKRLDETGVVRIPARGHLLDAHTVACSDGVRYSAEHILIATGAHPLRPDIPGAELGLVSDDFFDLRAAPAEVAIIGGGYIAVELAGLLQALGSKVSLLVRGQRLLDRFDYELTDQLAENLKQQGVRIHFGYRLRELQRDGERIRAFGHDGPLDSVFDAVFFATGRRGNSRDLGLEALGIGIGEHQQVQVDEWQTTSVPSVHAVGDIAGKVGLTPVAVAASRRLMDRLFGGRPQAKMDYENVASVVFSHPPLGAVGMSEEEARARFDQVSVYHSRFRPMLQALANGTQRSLFKMVCAGPDERVVGIHLLGEAADEILQGFAVAVKMGATKAQFDDTVAIHPTSAEEVVLMR
>NZ_CP021768.1|WP_087923232.1|3178236_3179487_-|FAD-dependent-oxidoreductase
MQGAHEDVIVVGAGAIGLAVALALRAQGRQVRVIDRGRVGGATSHGNCGTVTPSHAPPLAAPGVPLRALRWMLDPRAPLYVRTRLDPTLWRWLLQFGARCNARDWLHATRARGALLNDSRLRLADWVHTHALDCEFAARGLDYVFGDARNFDHHAAECEALNAQGIVTACIDGGDFARGNPAFHDRLAGAIHFPGDAQLRPDRYTVELARVLRAQGVVIDEQVNVQGFSDDAQGVRVQAGQQTVRARELVLATGPWSRDWARQLDLRVPIQPGKGYSLTWSRPAQVPLRPVVLKDHSVFVIAWRDALRLGGTMEFAGADPQLRTRRLQALQQAADHYLRAPRGAQLQEQWCGWRPMSVDDVPLIGRAPAHPHVWLAAGHGMLGISMSAGTGQLIADLVCGRTPAIDPAPYRPERFR
>NZ_CP021768.1|WP_087923233.1|3179490_3180735_-|DUF418-domain-containing-protein
MADLPDGPPVNAASPSLQPVASGERIAVLDVLRGAALLGILLMNIEAFSGPLDLAFTGIDVHWRGIDYWADAFVYVFVQGKFFTLFSLLFGAGFAVMAQRAEVAGRDFTPFYLRRSAGLLLIGLCHALLVWSGDILVMYALISLPLLACREAPRSWLPWMGLTVYLGGVAMMLLVGAMVSMASAEEVRGMLAEAQRSIDLQRQVYGQGSWAQANVQRLSEFGTSMGALLITGPEVLGMFLIGSWFAGSGALATPERFPRLYASLRWIALPLGLLVTLLGVAWKPYLAPGAYNLPVTAAMALVTVGGLPMCLGYLAWIVHWRARLAWLAPVGRMALTHYLGQSLLCTWTFYHYGLGRFEMMPRSVQLLFALLLFAAQVVISHLWLRHFRFGPIEWAWRAMTYRQWPPMRRGAGRG
>NZ_CP021768.1|WP_014647924.1|3180834_3181317_-|peptidylprolyl-isomerase
MKIEKDRVVRFHYTVSEVGQEPIESSKDRGEPLAILIGHGNIIPGLENAMMDKEAGATFNVDVKAADAYGERREGLSQRVPKKHFGNTKLAPGQQVVLQTNFGPRAVTVQKVGMSVVDVDLNHPMAGKDLHFDVEIVDVREAGKEELDHGHVHGDGGHQH

Crispr_ID: NZ_CP021768_10

• CRISPR_ID: NZ_CP021768_10
• CRISPR_location: 3846896-3847007
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_10

Consensus_repeat	Method
GTTGCCGGCCAGCGGCCGGCACTACCGG	CRISPRCasFinder

spacers of NZ_CP021768_10

>10.1|3846924|56|NZ_CP021768|CRISPRCasFinder
AGCAGCAGGATCAGGCGAGGATGCGGGCACGGCGTTCCTCGTCGCAGACGAGGGCT

CRISPR arrays and Neighbor proteins around NZ_CP021768_10

CRISPR arrays

The CRISPR arrays of NZ_CP021768_10

>merge|NZ_CP021768|10|3846896-3847007|CRISPRCasFinder
GTTGCCGGCCAGCGGCCGGCACTACCGGAGCAGCAGGATCAGGCGAGGATGCGGGCACGGCGTTCCTCGTCGCAGACGAGGGCTGTTGCCGCCCAGCGGCCGGCACTACCGG

>NZ_CP021768|10|9|3846896-3847007|CRISPRCasFinder
GTTGCCGGCCAGCGGCCGGCACTACCGG	AGCAGCAGGATCAGGCGAGGATGCGGGCACGGCGTTCCTCGTCGCAGACGAGGGCT
GTTGCCGCCCAGCGGCCGGCACTACCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_087923659.1|3844308_3846384_-|penicillin-binding-protein-2	unknown	unknown	gnl|CDD|274573
NZ_CP021768.1|WP_087923665.1|3855635_3855896_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087923662.1|3851083_3851815_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_005419400.1|3846387_3846873_-|rod-shape-determining-protein-MreD	unknown	unknown	gnl|CDD|225444
NZ_CP021768.1|WP_087923657.1|3842029_3843133_-|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_CP021768.1|WP_087923652.1|3834581_3835292_-|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl|CDD|237681
NZ_CP021768.1|WP_087923656.1|3839822_3840968_-|lytic-murein-transglycosylase-B	unknown	unknown	gnl|CDD|274066
NZ_CP021768.1|WP_087923663.1|3851942_3853871_-|M1-family-metallopeptidase	unknown	unknown	gnl|CDD|341062
NZ_CP021768.1|WP_014038522.1|3849418_3850357_+|carbohydrate-kinase-family-protein	unknown	unknown	gnl|CDD|238917
NZ_CP021768.1|WP_087923658.1|3843199_3844312_-|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_CP021768.1|WP_005419402.1|3848088_3849135_-|rod-shape-determining-protein	unknown	unknown	gnl|CDD|237562
NZ_CP021768.1|WP_087923654.1|3837224_3838445_-|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl|CDD|224600
NZ_CP021768.1|WP_087923653.1|3835895_3836969_+|lipid-A-deacylase-LpxR-family-protein	unknown	unknown	gnl|CDD|378338
NZ_CP021768.1|WP_087923655.1|3838545_3839826_-|septal-ring-lytic-transglycosylase-RlpA-family-protein	unknown	unknown	gnl|CDD|223868
NZ_CP021768.1|WP_087923664.1|3854984_3855437_+|nucleoside-deaminase	unknown	unknown	gnl|CDD|238612
NZ_CP021768.1|WP_005411067.1|3835279_3835558_-|YbeD-family-protein	unknown	unknown	gnl|CDD|179161
NZ_CP021768.1|WP_005411082.1|3854142_3854904_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	unknown	unknown	gnl|CDD|234689
NZ_CP021768.1|WP_032129005.1|3856374_3856797_+|low-affinity-iron-permease-family-protein	unknown	unknown	gnl|CDD|377225
NZ_CP021768.1|WP_087923661.1|3850460_3851084_-|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223620
NZ_CP021768.1|WP_014038526.1|3855971_3856298_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_087923659.1|3844308_3846384_-|penicillin-binding-protein-2	gnl|CDD|274573	TIGR03423, pbp2_mrdA, penicillin-binding protein 2. Members of this protein family are penicillin-binding protein 2 (PBP-2), a protein whose gene (designated pbpA or mrdA) generally is found next to the gene for RodA, a protein required for rod (bacillus) shape in many bacteria. PBP-2 acts as a transpeptidase for cell elongation (hence, rod-shape). [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	0
NZ_CP021768.1|WP_032129005.1|3856374_3856797_+|low-affinity-iron-permease-family-protein	gnl|CDD|377225	pfam04120, Iron_permease, Low affinity iron permease.	3.36649e-64
NZ_CP021768.1|WP_005419400.1|3846387_3846873_-|rod-shape-determining-protein-MreD	gnl|CDD|225444	COG2891, MreD, Cell shape-determining protein [Cell envelope biogenesis, outer membrane].	1.52102e-28
NZ_CP021768.1|WP_087923657.1|3842029_3843133_-|rod-shape-determining-protein-RodA	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	1.59996e-141
NZ_CP021768.1|WP_087923652.1|3834581_3835292_-|lipoyl(octanoyl)-transferase-LipB	gnl|CDD|237681	PRK14342, PRK14342, lipoyl(octanoyl) transferase LipB.	2.54248e-139
NZ_CP021768.1|WP_087923656.1|3839822_3840968_-|lytic-murein-transglycosylase-B	gnl|CDD|274066	TIGR02282, Membrane-bound_lytic_murein_transglycosylase_B, lytic murein transglycosylase B. This family consists of lytic murein transglycosylases (murein hydrolases) in the family of MltB, which is a membrane-bound lipoprotein in Escherichia coli. The N-terminal lipoprotein modification motif is conserved in about half the members of this family. The term Slt35 describes a naturally occurring soluble fragment of MltB. Members of this family never contain the putative peptidoglycan binding domain described by pfam01471, which is associated with several classes of bacterial cell wall lytic enzymes. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	7.20394e-137
NZ_CP021768.1|WP_087923663.1|3851942_3853871_-|M1-family-metallopeptidase	gnl|CDD|341062	cd09599, M1_LTA4H, Peptidase M1 family including Leukotriene A4 hydrolase catalytic domain. This model represents the N-terminal catalytic domain of leukotriene A4 hydrolase (LTA4H; E.C. 3.3.2.6) and the close homolog cold-active aminopeptidase (Colwellia psychrerythraea-type peptidase; ColAP), both members of the aminopeptidase M1 family. LTA4H is a bifunctional enzyme, possessing an aminopeptidase as well as an epoxide hydrolase activity. The two activities occupy different, but overlapping sites. The activity and physiological relevance of the aminopeptidase is poorly understood while the epoxide hydrolase converts leukotriene A4 (LTA4) into leukotriene B4 (LTB4), a potent chemotaxin that is fundamental to the inflammatory response of mammals. It accepts a variety of substrates, including some opioid, di- and tripeptides, as well as chromogenic aminoacyl-p-nitroanilide derivatives. The aminopeptidase activity of LTA4H is possibly involved in the processing of peptides related to inflammation and host defense. Kinetic analysis shows that LTA4H hydrolyzes arginyl tripeptides with high efficiency and specificity, indicating its function as an arginyl aminopeptidase. Thermodynamic characterization using different biophysical methods shows that structurally distinct inhibitors of the LTA4H occupy different regions of the binding site; while some (RB202, ARM1 and SC57461A) bind to the hydrophobic hydrolase side, both bestatin and captopril are located at the hydrophilic peptidase side. LTB4H overexpression is associated with different pathological conditions and diseases such as cystic fibrosis, coronary heart disease, sepsis, shock, connective tissue disease, and chronic obstructive pulmonary disease. It is also overexpressed in certain human cancers, and has been identified as a functionally important target for mediating anticancer properties of resveratrol, a well-known red wine polyphenolic compound with cancer chemopreventive activity.	0
NZ_CP021768.1|WP_014038522.1|3849418_3850357_+|carbohydrate-kinase-family-protein	gnl|CDD|238917	cd01942, ribokinase_group_A, Ribokinase-like subgroup A. Found in bacteria and archaea, this subgroup is part of the ribokinase/pfkB superfamily. Its oligomerization state is unknown at this time.	1.02439e-116
NZ_CP021768.1|WP_087923658.1|3843199_3844312_-|rod-shape-determining-protein-RodA	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	2.61211e-145
NZ_CP021768.1|WP_005419402.1|3848088_3849135_-|rod-shape-determining-protein	gnl|CDD|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0
NZ_CP021768.1|WP_087923654.1|3837224_3838445_-|D-alanyl-D-alanine-carboxypeptidase	gnl|CDD|224600	COG1686, DacC, D-alanyl-D-alanine carboxypeptidase [Cell envelope biogenesis, outer membrane].	4.3282e-148
NZ_CP021768.1|WP_087923653.1|3835895_3836969_+|lipid-A-deacylase-LpxR-family-protein	gnl|CDD|378338	pfam09982, DUF2219, Uncharacterized protein conserved in bacteria (DUF2219). This domain, found in various hypothetical bacterial proteins, has no known function.	8.28338e-107
NZ_CP021768.1|WP_087923655.1|3838545_3839826_-|septal-ring-lytic-transglycosylase-RlpA-family-protein	gnl|CDD|223868	COG0797, RlpA, Lipoproteins [Cell envelope biogenesis, outer membrane].	3.11074e-54
NZ_CP021768.1|WP_087923664.1|3854984_3855437_+|nucleoside-deaminase	gnl|CDD|238612	cd01285, nucleoside_deaminase, Nucleoside deaminases include adenosine, guanine and cytosine deaminases. These enzymes are Zn dependent and catalyze the deamination of nucleosides. The zinc ion in the active site plays a central role in the proposed catalytic mechanism, activating a water molecule to form a hydroxide ion that performs a nucleophilic attack on the substrate. The functional enzyme is a homodimer. Cytosine deaminase catalyzes the deamination of cytosine to uracil and ammonia and is a member of the pyrimidine salvage pathway. Cytosine deaminase is found in bacteria and fungi but is not present in mammals; for this reason, the enzyme is currently of interest for antimicrobial drug design and gene therapy applications against tumors. Some members of this family are tRNA-specific adenosine deaminases that generate inosine at the first position of their anticodon (position 34) of specific tRNAs; this modification is thought to enlarge the codon recognition capacity during protein synthesis. Other members of the family are guanine deaminases which deaminate guanine to xanthine as part of the utilization of guanine as a nitrogen source.	1.21869e-42
NZ_CP021768.1|WP_005411067.1|3835279_3835558_-|YbeD-family-protein	gnl|CDD|179161	PRK00907, PRK00907, hypothetical protein; Provisional.	1.56476e-63
NZ_CP021768.1|WP_005411082.1|3854142_3854904_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	gnl|CDD|234689	PRK00216, ubiE, bifunctional demethylmenaquinone methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol methylase UbiE.	5.68803e-138
NZ_CP021768.1|WP_087923661.1|3850460_3851084_-|HAD-family-hydrolase	gnl|CDD|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	6.17375e-29

Protein sequences

>NZ_CP021768.1|WP_005419400.1|3846387_3846873_-|rod-shape-determining-protein-MreD
MSRLRDNPWVLPASLVVALLLGLLPLPALLQPLRPYWLALVLAYWVIEAPERVGLGIAFASGVVADLLYGGVLGEQALRLVMLAFILQRFRARIRFFPMSQQMLAIGGLLFNDRIVSALVHIVVDEPTLPWSYWWAPLLGMGLWPLVFVLLDAVRFGKRGR
>NZ_CP021768.1|WP_087923659.1|3844308_3846384_-|penicillin-binding-protein-2
MIPRRQVKNPHAEAEQFRRRAALGFLGVLVCLLGLGGWYFKLQVLDHDVYATRSEANRIKPRPVVPGRGMIYDRNGRLLAENVPAFRLDVTPDKVKDMDATLEGLAKIITISPEELEAFNKSRKARRKFLPVTLKLRMSDEEMARFAVDRWRFPGVELEPYLTRRYPYGDLFAHIIGYVGRVDDKDLEILGEGNAALTHIGKSGLERYYEQQLRGKVGYEQVETNVQGRAIRTIGRVAAQSGADLRLSIDADLQRAMVAAFGDQEGSAVAMDPRTGEVLAMVSLPSYDPNLFVNGISHADFKALNENPSRPQFNRLVLGGVAPGSTLKPLIGLAGLDSGVRRPEDKVLSTGMFYLPGTSRGWGDSHRGGHGWTDLRKSIAQSVNTYYYKLALDLGIERFDHYMEYYGFGQPTGIDLTGEIGGILPSPAYKRKSRKEAWYPGDTVNISIGQGDWKVTPLQLARGVSGLADGQLRTPHLVIQQRAGFDHDWMATDPGESKPISPNPNNLQAVREGMMATMLPGGSAARMAAGAPYTMAGKTGTAQVISRKGTAAVNPKSLPMHLRHRALFVGFAPVDRPVIALAIAVEGGGYGGAAAAPIARKVFDAYLLGKMPEGMQPLDSERGTTAIGATAFDNEDAGARQAGDFAAAQLGEHPVLVGVPAPEPAPAPQPGTPAAAALPATPRPTPAEPAR
>NZ_CP021768.1|WP_087923658.1|3843199_3844312_-|rod-shape-determining-protein-RodA
MRVFLRWAGDMLRRFFSTLDWVLCLALGALMLIGLATLKSAGGDGLVMAQGARFAVGMAALWGISRVPILRIRSATPMIYAISMIPLLAVFVLGTGKYGRQWLDLKFFYLQPAELLKVSLPMMVAWYLHKMPLPPRFNTVLTALVIIGVPTGLVMLQPDFGTGVLIAASGVFVLLLAGLPWWWVGLGVGGVAAVAPVAWFWLLRPYQKDRIMMFLDPEMDALGAGWNIIQSKIAIGSGGFDGKGWGEGSQSHLNFIPEQTTDFAFSVLSEEFGWIGVATVLALYLVVIGRCLWIASQSRDSYSRLLAGATGLAFFVYVLVNGGMISGLLPVVGVPMPLISYGGTSAVSLLAGFGLVMAVRSHNPVHGGYG
>NZ_CP021768.1|WP_087923657.1|3842029_3843133_-|rod-shape-determining-protein-RodA
MLCVEWKRLLGGCREVVRTIDLPLLVALLMLMGAGLAVLHSVSGPVGGQAARFAGGLLAMWLLSRVSLLRLRAWTPALYALSMLPLMAVYVIGTGKYGQRWLNLGVFYLQPSELLKLSLPLMMAWYLHRQPLPPSPRTVLTAAVLIGLPAVLILMQPNLGTATLVTASGVFALLLAGLHWGWVATGAAGLAVAAPLAWFGLLRPYQKDRVLTFLDPAADPLGTGWNILQSRIAIGSGGWQGRGWGQGTQATLDFLPEYTTDFAFSVLAEEFGWLGVATLFALYLFVVGRCLWIAVHARDTHARLLAGSLGLAFFVYVLVNGGMISGLLPVVGIPMPLISYGGTSAVSLLAGIGLVMAVRGHRPVHGG
>NZ_CP021768.1|WP_087923656.1|3839822_3840968_-|lytic-murein-transglycosylase-B
MIRRTLACMLTLGLVACATQPKSPPSSPQASSTPRQPAAKAHGPAEAAPEAAAATAPPVDLTPVPFEVARARFIADTAKRYGLKPEQISSVLDQAQVRQPIIAAMSRPAERVKPWNEYRPMFISKARIDGGRAFLAQHRAELDRVQQRTGVPAEVIVAIIGVETSYGKNAGSHRVLDALYTLAFYYPRSGDPAKLEREVRRELFFRDELAKLFELGREEKLDITTLKGSYAGAMGMGQFMPSSYLDYAVDGNGDGRRDLFTSYDDVFSSIANYFVKKGGWVRGGQVAVPATLAPGREEFNPTEWMPTWSMADLAQRGYQPGAPVQPGTTATPITLEGSTGKQYWLGFQNYYAITRYNLSKMYAMAVFQLSQAIAGQELPPA
>NZ_CP021768.1|WP_087923655.1|3838545_3839826_-|septal-ring-lytic-transglycosylase-RlpA-family-protein
MNIRWLVSGLIVLALAACSSAPKKPATAGHGGKSGGTLVQGRGSRPAHCPEGSPYAAAKEDLSTRGNYTAGGLYKPGVRDSTPDYVPNVACIPEPEVTAEERSAIGNKSPYVVLGKSYKVLDDTRNYVERGTASYYGAKFHGRLTSNREVYDMYQFTAAHKTLPLPSFARVTNLDNGESVIVRVNDRGPFHDGRVVDLSYAAAVRLGITQRGTGNVEVRALQPGESNLLAQKPSRRERRAAEAAAASTVMASARPAPTARATADSDIDRLVKGLPADGMPARGQPATTQGVASTVPDVAVSSLPPSAPPVRSTAPAPVAVASATPRAVAPAPVRTVAATPAAPSLSQQVVGAVMVQVASFSNRDNANRAMGQLNAAGIVGATISDIAAGGRTLFRLRVPANDHASAAELVGRIAGLGLGSPQIVKD
>NZ_CP021768.1|WP_087923654.1|3837224_3838445_-|D-alanyl-D-alanine-carboxypeptidase
MNFRSAATALAATLVVGLASAQTPLPTPATPAPAAAAAAPATVATPPAPAPSVSKAWVLMDYATGQVLAGENVHEQLAPASITKVMTSYVIAAEVKNGKVRADDQVMMSERAWREGGAGTDGSYSGFPVNQTARLEDMEKGMAIQSGNDAAIALAEHVAGSEEAFASLMNSYAAKIGMKDSHFVNAHGLTAEGHHSTAYDLALLGRAMVRDYPETYAYNKIKEFQVGNIKQPNRNLLLWRDGSVDGIKTGHTSEAGYCLMSSAQRGDQRLIAVVLGGASEKQRADDSLALLNWGFRFFETHRLYEPGKAVAEHKVWKGTTDKVQLGVAQPMLVSVPRGRYSDLKPSIDVPKTLEAPFTAGQQIGTVKVTLDGKVIAEAPLVAVAAVEQAGFFKRLWDSFWMWWESE
>NZ_CP021768.1|WP_087923653.1|3835895_3836969_+|lipid-A-deacylase-LpxR-family-protein
MSIPSMRSVAALGLAGLLASAFPFAAQAAEQCGPDAMRDHPPQVNFRVDNDLFGGRHQDQGYTNGALLTLVSPNLVDYTDDPCLPRMARWVNQYLEGLHPGRFEQQNMIFSIGQGIFTPTDFSRRDLIEDDRPYAGVLIANFGFNARSGDRLQTTQLTLGVVGPWAQGRQVQNAVHAVLGDEKFKGWDNQLHNEPLFMLTHERMRRWPGDASINADGWGWDAISHYGGSIGNLETKANFGGEVRFGWKLPDDFGSTPLRPAGENTAPTRGGRPNGWSWHLFATSDVAWVIRDITLDGNTFRNSHSVDKRHVVAYGGYGVAVMRGRWKFAMARYHSTREFNGQREAPVFGSFTISRSL
>NZ_CP021768.1|WP_005411067.1|3835279_3835558_-|YbeD-family-protein
MEIKSDNPDHGFQFPGQFELSAMGPANRGLEHELPRLLLAAGIDVVNERISWKHSSNGKYVSVRIVFKAESREQYDLAHQALRDHPEVKWTL
>NZ_CP021768.1|WP_087923652.1|3834581_3835292_-|lipoyl(octanoyl)-transferase-LipB
MDAVAGSCPAEAAPEDRAPRPAVVRDLGRQAYEPVWRAMQRFTDQRSEADADELWVVEHDPVFTLGQAGKDEHVLAPGEIPVLHVDRGGQVTYHGPGQIVVYPLLRLPRLGIGVRDYVCRIEQALIDTLAEWNIGAERREGAPGVYVGGAKIAALGIRVRRGCTFHGLAFNVAMDLEPFHRINPCGYQGLQVTSVVDLGGPSGMDAVKPVLLDHLARQFGLLLQHTPELPDLSAAA
>NZ_CP021768.1|WP_005419402.1|3848088_3849135_-|rod-shape-determining-protein
MFKKLRGMFSNDLSIDLGTANTLIYVRGQGIVLNEPSVVAVRQDRAIGGTRSVAAVGAEAKQMLGRTPGHITTIRPMKDGVIADFTYTEAMLKHFIKKVHKSRVLRPSPRVLVCVPAGSTQVERRAIKESAEEAGARDVFLIEEPMAAAIGAGMPVTEARGSMVIDIGGGTTEVAVISLNGIVYSASVRIGGDRFDESITNYVRRNHGMLIGEATAERIKVELGCAYPQAEVIEMEISGRNLAEGVPKMIKISSNEVLEALHEPLSGIVSAVKLALEQTPPELCADVAERGIVLTGGGALLRDLDRLISEETGLHVQVADDPLTCVARGGGRALELVDMHGNEFFAPE
>NZ_CP021768.1|WP_014038522.1|3849418_3850357_+|carbohydrate-kinase-family-protein
MSALICGSLAFDTIMVFPDQFKNHILPDKVHILNVSFLVPRMRREFGGCAGNIAYNLHLLGGQPIPMGTVGSDFGPYREYFDGLGIDLSRVRVIDELFTPQAFITTDHDNNQITAFHPGAMMRSYENHVRGVPGVTLGLVGPDGREGMIQNAQEFHEDGIPFIFDPGQAMPLFNGPELRAFIEQADYVVVNDYESNLLQERTGWDEKEIVSRVKAYITTRGPKGAVIHTPEKSYDIPPAHERRVVDPTGCGDAFRAGLIYGIQKGYDWLTIGRMGNLMGALKVEHPGTQNQRFTFDEFNEQFKQQFGYALGA
>NZ_CP021768.1|WP_087923661.1|3850460_3851084_-|HAD-family-hydrolase
MIAAGSAVHALSAIRHWVFDMDGTLTVAVHDFAAIRRALQIAAEEDILDHIAALPDAPAQAKREWLLDHERALAEDALPAPGAVKLLRALSAAGCRLGILTRNDHALAKLTLDAIGVGELFDDADIIGRDEAVPKPSPDGLQQHLRRWGIGAAEAVMVGDHAYDLECGRAAGTRTVLVNLPENPCPGRADWHFADCRDLLAAWQQKG
>NZ_CP021768.1|WP_087923662.1|3851083_3851815_-|hypothetical-protein
MKRLILLTACTLALAACSNPEEERKAQEAAAAAVQAQKEAKAEDVAKQYEMAVAAQDWERARLHGASLLDQYKDTAAAERIAAGFDEVKAKGDAARDLRRMQALWQYNQIPVGNKGNQVSAQIYSKERVDVDGSGAKPVQLVFRDHPEWKRHAYLVLQAGDFRCPQCTVKVTVDDGKPVSMAAWRPKTDEAIALFITDQKALWKLARKGKSISIEFPVKAGGTRTAVFETGGVDASRMPQWWQ
>NZ_CP021768.1|WP_087923663.1|3851942_3853871_-|M1-family-metallopeptidase
MRNPLMLLPLAVALAAGCSQEAAAPAAAPTAAKAPAAPVNAENRSHDESSYAEPDKVVIKDIALDLKLDFDQKQIGGTATYTLEWKQKDAKQLVLDTRELTVSKVEAVAADGARSALQFELAPVDKVFGSKLTIEAPEQPAKVEVTYHTAPTASGLQWLAPSMTEGKKLPFMFSQSQAIHARSWVPLQDTPSVRFTYSAHVVSRPDVMVLMSADNDPKAARDGDYTFKMPQPIPSYLLAIAAGDLVFEPISGRSGVWAEPTMVNKAAKEFEDTEKMIGAAEKLYGEYRWGRYDMLVLPPSFPFGGMENPRLTFATPTVIVGDKSLVSLVAHELAHSWSGNLVTNASWKDIWLNEGFTTYVQGRITEALYGKEMAEMEKQIDQTDLLAEVKDMSPADQALALPPLNERDPDEALSQVAYVKGSWFLEFLEQRFGRETFDPFLRGWFDDHAFQSANTDQFVEYMKKNLLPKNPSAVTEAELKAWLDEPGIPAFAAKAQSRNFSSVDTARIAFASAGTVPSSQVIADWSTQEWVRFIDGLGATQPLDKLATLDKAFHFTGTPNGEIAMRWYPLAIRSGYEQANEGAAAFIERVGRRKLILPIYAELVKTPKGLELAKQAFEKAKPGYHPITTASVQDMLAKAEAK
>NZ_CP021768.1|WP_005411082.1|3854142_3854904_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE
MSESPYKAGTTHFGFRDVAAKDKQKLVGQVFTSVARNYDLMNDLMSLGVHRAWKRYYVATAQVKPGDRVLDLAGGTGDIAALLKERVGAEGSVVLGDINAGMLSVGRDRLTNRGLVLGLDYVQCNAEALPFPDNSFDLVTIAFGLRNVTDKDAGLREMYRVLKVGGQARVLEFSEVTADWFKPIYDFHSFKILPKLGKLFANDSDSYQYLAESIRKHPPQDELKAMMGQAGFERCHYKNLTGGIVSIHSGYKL
>NZ_CP021768.1|WP_087923664.1|3854984_3855437_+|nucleoside-deaminase
MITTPDYQTLLQTAIAEARQGLAEGGVPIGAALYHNDGRLLGCGHNRRVQEGDPSVHGETDAFRKAGRQRRYQDTIMVTTLAPCWYCSGLVRQFNIGTVVVGESRTFQGGIDWLRENGVNVIDLDNQECVDLLGDFISRHPDIWNEDIGE
>NZ_CP021768.1|WP_087923665.1|3855635_3855896_+|hypothetical-protein
MCAHAVRPTPDPILDAIRERLQQQYALHQRGALFWTAYQGLQLELVRGHPLDHERLCNAMADMAENLGAVEHAQLIGNRNAGSTSR
>NZ_CP021768.1|WP_014038526.1|3855971_3856298_+|hypothetical-protein
MHAEVPTIPPVINVDAELDHWRRQHADGALPHNSFGSYVPWIKFACDSLITQPRASNAQRDEMFQTQYALQIMPRLSEAQAREFVDRCWQHVYQTSPVRLQDAPRLRA
>NZ_CP021768.1|WP_032129005.1|3856374_3856797_+|low-affinity-iron-permease-family-protein
MKARNLFNTIAKKAAAATGSPWTFLAAVAIVVIWGISGPVFGFNDTWQLVINTGTTIITFLMVFLIQHTQNADTAAMQIKLDELIRATAEANNELLDLEELDEERLEEIRREYEQMAREAGDALARVRACHAARRDDEAV

Crispr_ID: NZ_CP021768_11

• CRISPR_ID: NZ_CP021768_11
• CRISPR_location: 4114292-4114400
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP021768_11

Consensus_repeat	Method
TCAGAATCCGTGCCGACCAAGGTCGGCACCTACC	CRISPRCasFinder

spacers of NZ_CP021768_11

>11.1|4114326|41|NZ_CP021768|CRISPRCasFinder
AAGAGCGGCAACCGGTAGATCCACGCCATGCGTGGATACGG

CRISPR arrays and Neighbor proteins around NZ_CP021768_11

CRISPR arrays

The CRISPR arrays of NZ_CP021768_11

>merge|NZ_CP021768|11|4114292-4114400|CRISPRCasFinder
TCAGAATCCGTGCCGACCAAGGTCGGCACCTACCAAGAGCGGCAACCGGTAGATCCACGCCATGCGTGGATACGGTCAGGATCCGTGCCGACCAAGGTCGGCACCTACC

>NZ_CP021768|11|10|4114292-4114400|CRISPRCasFinder
TCAGAATCCGTGCCGACCAAGGTCGGCACCTACC	AAGAGCGGCAACCGGTAGATCCACGCCATGCGTGGATACGG
TCAGGATCCGTGCCGACCAAGGTCGGCACCTACC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP021768.1|WP_006399171.1|4111070_4111355_+|K+/H+-antiporter-subunit-F	unknown	unknown	gnl|CDD|180435
NZ_CP021768.1|WP_087923847.1|4118994_4119594_-|disulfide-bond-formation-protein-DsbD	unknown	unknown	gnl|CDD|379399
NZ_CP021768.1|WP_087923845.1|4114403_4115711_-|homogentisate-1,2-dioxygenase	unknown	unknown	gnl|CDD|235421
NZ_CP021768.1|WP_087923842.1|4111828_4112794_-|sodium:calcium-antiporter	unknown	unknown	gnl|CDD|223604
NZ_CP021768.1|WP_087923848.1|4119613_4121113_-|MFS-transporter	unknown	unknown	gnl|CDD|225646
NZ_CP021768.1|WP_042359011.1|4117056_4117551_+|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_CP021768.1|WP_014038751.1|4110567_4111074_+|Na+/H+-antiporter-subunit-E	unknown	unknown	gnl|CDD|181598
NZ_CP021768.1|WP_087923849.1|4121294_4122170_-|tryptophan-2,3-dioxygenase	unknown	unknown	gnl|CDD|188272
NZ_CP021768.1|WP_049443927.1|4111351_4111741_+|Na+/H+-antiporter-subunit-G	unknown	unknown	gnl|CDD|237169
NZ_CP021768.1|WP_087923844.1|4113646_4114195_+|hypothetical-protein	unknown	unknown	gnl|CDD|171499
NZ_CP021768.1|WP_005411349.1|4124649_4125003_+|hypothetical-protein	unknown	unknown	gnl|CDD|212789
NZ_CP021768.1|WP_087923839.1|4105000_4105486_+|DUF962-domain-containing-protein	unknown	unknown	gnl|CDD|226914
NZ_CP021768.1|WP_042359306.1|4115814_4116885_-|4-hydroxyphenylpyruvate-dioxygenase	unknown	unknown	gnl|CDD|225726
NZ_CP021768.1|WP_087923843.1|4112867_4113521_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087923841.1|4109035_4110571_+|monovalent-cation/H+-antiporter-subunit-D	unknown	unknown	gnl|CDD|237166
NZ_CP021768.1|WP_049401674.1|4108646_4109039_+|Na+/H+-antiporter-subunit-C	unknown	unknown	gnl|CDD|236377
NZ_CP021768.1|WP_087923840.1|4105818_4108647_+|monovalent-cation/H+-antiporter-subunit-A	unknown	unknown	gnl|CDD|237157
NZ_CP021768.1|WP_087923846.1|4117632_4118772_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP021768.1|WP_087924242.1|4123661_4124648_+|alpha-ketoacid-dehydrogenase-subunit-beta	unknown	unknown	gnl|CDD|223101
NZ_CP021768.1|WP_087923850.1|4122505_4123588_+|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	unknown	unknown	gnl|CDD|213783

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP021768.1|WP_006399171.1|4111070_4111355_+|K+/H+-antiporter-subunit-F	gnl|CDD|180435	PRK06161, PRK06161, putative monovalent cation/H+ antiporter subunit F; Reviewed.	9.48908e-36
NZ_CP021768.1|WP_087923847.1|4118994_4119594_-|disulfide-bond-formation-protein-DsbD	gnl|CDD|379399	pfam13899, Thioredoxin_7, Thioredoxin-like. Thioredoxins are small enzymes that participate in redox reactions, via the reversible oxidation of an active centre disulfide bond.	0.000638657
NZ_CP021768.1|WP_087923845.1|4114403_4115711_-|homogentisate-1,2-dioxygenase	gnl|CDD|235421	PRK05341, PRK05341, homogentisate 1,2-dioxygenase; Provisional.	0
NZ_CP021768.1|WP_087923842.1|4111828_4112794_-|sodium:calcium-antiporter	gnl|CDD|223604	COG0530, ECM27, Ca2+/Na+ antiporter [Inorganic ion transport and metabolism].	2.43034e-43
NZ_CP021768.1|WP_087923848.1|4119613_4121113_-|MFS-transporter	gnl|CDD|225646	COG3104, PTR2, Dipeptide/tripeptide permease [Amino acid transport and metabolism].	2.91358e-141
NZ_CP021768.1|WP_042359011.1|4117056_4117551_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	7.64801e-16
NZ_CP021768.1|WP_014038751.1|4110567_4111074_+|Na+/H+-antiporter-subunit-E	gnl|CDD|181598	PRK08965, PRK08965, putative monovalent cation/H+ antiporter subunit E; Reviewed.	2.27879e-62
NZ_CP021768.1|WP_049443927.1|4111351_4111741_+|Na+/H+-antiporter-subunit-G	gnl|CDD|237169	PRK12674, PRK12674, putative monovalent cation/H+ antiporter subunit G; Reviewed.	6.64372e-33
NZ_CP021768.1|WP_087923844.1|4113646_4114195_+|hypothetical-protein	gnl|CDD|171499	PRK12438, PRK12438, hypothetical protein; Provisional.	0.000259816
NZ_CP021768.1|WP_005411349.1|4124649_4125003_+|hypothetical-protein	gnl|CDD|212789	cd11855, SH3_Sho1p, Src homology 3 domain of High osmolarity signaling protein Sho1p. Sho1p (or Sho1), also called SSU81 (Suppressor of SUA8-1 mutation), is a yeast membrane protein that regulates adaptation to high salt conditions by activating the HOG (high-osmolarity glycerol) pathway. High salt concentrations lead to the localization to the membrane of the MAPKK Pbs2, which is then activated by the MAPKK Ste11 and in turn, activates the MAPK Hog1. Pbs2 is localized to the membrane though the interaction of its PxxP motif with the SH3 domain of Sho1p. SH3 domains are protein interaction domains that bind to proline-rich ligands with moderate affinity and selectivity. They play versatile and diverse roles in the cell including the regulation of enzymes, changing the subcellular localization of signaling pathway components, and mediating the formation of multiprotein complex assemblies.	7.24408e-09
NZ_CP021768.1|WP_087923839.1|4105000_4105486_+|DUF962-domain-containing-protein	gnl|CDD|226914	COG4539, COG4539, Predicted membrane protein [Function unknown].	1.15916e-15
NZ_CP021768.1|WP_042359306.1|4115814_4116885_-|4-hydroxyphenylpyruvate-dioxygenase	gnl|CDD|225726	COG3185, COG3185, 4-hydroxyphenylpyruvate dioxygenase and related hemolysins [Amino acid transport and metabolism / General function prediction only].	4.01598e-153
NZ_CP021768.1|WP_087923841.1|4109035_4110571_+|monovalent-cation/H+-antiporter-subunit-D	gnl|CDD|237166	PRK12666, PRK12666, putative monovalent cation/H+ antiporter subunit D; Reviewed.	0
NZ_CP021768.1|WP_049401674.1|4108646_4109039_+|Na+/H+-antiporter-subunit-C	gnl|CDD|236377	PRK09094, PRK09094, putative monovalent cation/H+ antiporter subunit C; Reviewed.	7.26377e-63
NZ_CP021768.1|WP_087923840.1|4105818_4108647_+|monovalent-cation/H+-antiporter-subunit-A	gnl|CDD|237157	PRK12648, PRK12648, putative monovalent cation/H+ antiporter subunit A; Reviewed.	0
NZ_CP021768.1|WP_087923849.1|4121294_4122170_-|tryptophan-2,3-dioxygenase	gnl|CDD|188272	TIGR03036, trp_2_3_diox, tryptophan 2,3-dioxygenase. Members of this family are tryptophan 2,3-dioxygenase, as confirmed by several experimental characterizations, and by conserved operon structure for many of the other members. This enzyme represents the first of a two-step degradation to L-kynurenine, and a three-step pathway (via kynurenine) to anthranilate plus alanine. [Energy metabolism, Amino acids and amines].	3.47115e-131
NZ_CP021768.1|WP_087924242.1|4123661_4124648_+|alpha-ketoacid-dehydrogenase-subunit-beta	gnl|CDD|223101	COG0022, AcoB, Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit [Energy production and conversion].	9.03877e-165
NZ_CP021768.1|WP_087923850.1|4122505_4123588_+|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	gnl|CDD|213783	TIGR03181, PDH_E1_alph_x, pyruvate dehydrogenase E1 component, alpha subunit. Members of this protein family are the alpha subunit of the E1 component of pyruvate dehydrogenase (PDH). This model represents one branch of a larger family that E1-alpha proteins from 2-oxoisovalerate dehydrogenase, acetoin dehydrogenase, another PDH clade, etc. [Energy metabolism, Pyruvate dehydrogenase].	3.12606e-175

Protein sequences

>NZ_CP021768.1|WP_087923844.1|4113646_4114195_+|hypothetical-protein
MQPRKTDLARTALQAHRAPLDMRQRRLLILCDGQRSIADLTGLLGPEAPAMVIQLVQAGYLSTGTAATTPPPSPAPAAAPVPPAPPSAAPVATLATAVERRRSLVAARIYVLGILEMQRHPQAAALFGDLQQARAESEVLQVLHSAMQMLPGLTSEGYCQRVRQRLLEALPLEHCDAFAEVA
>NZ_CP021768.1|WP_087923843.1|4112867_4113521_-|hypothetical-protein
MKHLPLAGLLLLSLTACGGHDKQGAAGSGSDTPAETASATGPAQSTDPDLAARPANDRREDSPARLDGFAGAKLGAGIAEVRSGFGTPLQGLGTDASGKPLRADDGNDGCYFLRPQDAEDPRLMIEGRKLVRYDVRSAAIAAPGGGKVGMTLGELQVLYPERGDVGPDKYDDKAQHLRVRPAQEGGAVIDFALGADGRVGAWRVGQTPQVDYVEGCG
>NZ_CP021768.1|WP_087923842.1|4111828_4112794_-|sodium:calcium-antiporter
MITIAIAWFLLGLLLLALGGDSIVKAVSGLAQRFGASPFTAGLLLLGVATSLPELAVNARALAVGQPELALGNAVGSSIVNLGLTLAVAAIAAPLLLRARLQAVLWWSLLAAGILLILFGLDGRLARWEGGVLVAGFIVMQVLLLRRGRVESVEVQAAIAESALSRTSLPLNVLRVLIAALTLYWGARLVVGAAADFGAALGWTPLLVGLLPVAIGTALPEVATAIAAARRGHGHMVLGHVLGSSVVNLLLVIGAMAMLQPLALPASFVRLELPALLAFALVLYPMLRGDLKISRSEGGILLVAFVGWFVLELLLVGAPAL
>NZ_CP021768.1|WP_049443927.1|4111351_4111741_+|Na+/H+-antiporter-subunit-G
MITAIQIGLSILLLFGCFFILVGALGLVKLSTFFKRLHAPTKASTLGVGCVLVCSVCYHIFLGQDPQPRELLITVFLFITAPISAHMMAKAALSLLMETRPSLPGNEPAAEEQLPPPEPVREEEHAQNR
>NZ_CP021768.1|WP_006399171.1|4111070_4111355_+|K+/H+-antiporter-subunit-F
MTGFQIIQTTLVVCMHVVGLAMLLATWRLLRGPTVPDRILALDTLSVTAIAELMLFGMYLNSAIYFEAALVIAMLGFGSTVVLSKFVLRRDIVE
>NZ_CP021768.1|WP_014038751.1|4110567_4111074_+|Na+/H+-antiporter-subunit-E
MTAQRSLFRRLIPSPMLSIMVVAFWLLMSDSFTLGQIVLGLLLGVVVPLFAARLDREFARIGTLRPLPKLLCVTLWDILMSNIRVAIQVLGPEKNIHPGFIWLPLDIANIHGIAALTSMITLTPGTVSAALSDDRKFLLVHVLHLEDPQDLIDTIKRRYEAPLMEIFP
>NZ_CP021768.1|WP_087923841.1|4109035_4110571_+|monovalent-cation/H+-antiporter-subunit-D
MNHLVILPILIPLLGAALSLFVEHRRYGPRVQRAVAWTALSALALAVGLLFASTAGGDINVYLLGDWPSRLGIALVADRLSAWMLLTTLLLAIPCLLHACSGWDRRAPHFHALFQFQLVGLNGAFLTGDIFNLFVFFEVMLIASYGLLLSGGRGLRMRIGLHYVVFNVTASTLFLIALGLLYASLGSLNMAELSQRIAEVPPAQLTLVKATMGLLLLVFCAKAALMPLYLWLPEAYSRAPAAVAAMFAIMTKVGLYSVLRIQMLWFGDDAGAMAGYGRDWLLWAGVATLVLGGLGALAATRLRVLISYLVIVSAATLFIAFSVGTPKVLSAGLYYLPHSSFVAAALFLIADLIRRRRGGASDRKEVVAPMPGKETPAVLFLIGAVSVAGLPPLSGFLAKAALLAGMPAQYTGPVWTAVLVSSLLVIMGLTRGGIRLFWRVPPVDPEAPMPRKARLRRVELYAACILLAYGIAMTLAAAPLTRYTDATAAQLLQPSEYVQQLRATTPEIRQP
>NZ_CP021768.1|WP_049401674.1|4108646_4109039_+|Na+/H+-antiporter-subunit-C
MELALATAIGVLTAIGIYLLLRARSFDVILGMTFLSYATNLLIFAGGRVVLGKAPVLQEGVDSHLGNYTDPLPQALVLTAIVIAFAMTAVSIVLAMRSRSDNHSDHVDAHEPDDDLQDERMPPRQGEDRA
>NZ_CP021768.1|WP_087923840.1|4105818_4108647_+|monovalent-cation/H+-antiporter-subunit-A
MLPSLPLLLALPFLMAAAVAAFPRSSRSTAAWLAALAPLGGLAILAWLTPSVLDGQVVRTLVPWLPQIGLDFTLRLDGLAWMFAGLVLGIGALVVLYARYYLSQQDNAHRFYCYLLLFMGAMLGMVLSGNLLLLMIFWEMTSISSFLLIGFWSHRQDAREGARMALVITGGGGLALLGGVLLIGRIVGSFDLDVVLAAGEQIRASALYPYALFLVLAGIFTKSAQFPFHFWLPHAMAAPTPVSAYLHSATMVKAGVFLLARLHPALAGSDLFFYTVSGVGALTLLIGAWNAIFQHDLKGLLAYSTISHLGLITLLFGLSTPMAVVAGVFHILNHATFKASLFMAAGIIDHETGTRDMRKLGGLRRLMPFTSALAIIASLAMAGIPLLNGFLSKEMLFAEAITAGGPGIMRAAVSIAALLAGVFGVAYSLRFVHDTFFGPGPHELDRVPHEPPRWMKVPVELLVVICIAVGVAPALTVAPVLHAAAASILGNAMPEYSLAVWHGFNLPLAMSAIGVVGGVALYFGLRKLINLHGVTNVSTGRNVFHAQLDAVSALAMRLTNGIANGSLQRMLLGLVLVAIVVAAAPFVANPASPNWTAPQPIPLLGWALWLVMMACAVATLRVYKQRLLAVLLVGGVGLMVALTFVFLSAPDLALTQLLVEMVTLVLMLLGMNYLPAQSGPERPRWRKRRDAVIAIIAGAGLGALAYSAMTLPPNTMAGELLARALPEAYGQNVVNVILVDFRGFDTFGEITVFGIAALVVHALLRRTRMAPEQIMPGPPIKLPVPADLAQIMFPLTLTVSIFLFLRGHNAPGGGFIAGLVLAVPLLIQYVIQGTASVESRFGFDYIRCIGMGLLIAILSGSASMLFGVPFLTSGHLDLHLPLIGDVPLASAIGFDIGVYLVVFGGAMLMLSMMATVKPSRTRTARKGEIDLQRRSARTGEMH
>NZ_CP021768.1|WP_087923839.1|4105000_4105486_+|DUF962-domain-containing-protein
MQTSTELARPIDRYFASYSDDHRNVINQRIHVVAVPAILWSVVALLWCLPPLITWFQYGIWSAFAMFSAWCFYNKLSRPLGIGMLIQFFVFGCLCRLLEAEIGIQALRWLAVGVFVVAWIAQFIGHTFEGRKPSFLTDLTYLLIGPAWVMAKFYRKLDWRY
>NZ_CP021768.1|WP_087923845.1|4114403_4115711_-|homogentisate-1,2-dioxygenase
MSPAITARGYQSGFGNEFATEAVAGALPVGQNSPQKVAHGLYAEQLTGTAFTAPRGSNRRSWLYRIRPAVTHGEFTPFAQSQLQCDFGAQPASPNQLRWSPLPLPALPTDFVEGLYTMGGNGSPDAHAGVGIHLYAANRDMVGRYFYDADGELLIVPQLGALRLLTELGVIEIEPQQIAVIPRGVRFRVELPDGPSRGYICENYGALLKLPDLGPIGSNGLANPRDFETPHAAFEDVDGDFELIAKFEGRLWRAPIDHSPLDVVAWHGNYAPYRYDLRRFNTIGSISYDHPDPSIFLVLHSPSDTPGTSNMDFAIFPPRWLVAQNTFRPPWFHRNIASEFMGLVHGAYDAKAEGFVPGGASLHNCMSGHGPDAPTFDKASNADLSKADVIKDTMAFMFETRAVIRPTAQALAAGHRQGDYQQCWNGLRNNYRSSR
>NZ_CP021768.1|WP_042359306.1|4115814_4116885_-|4-hydroxyphenylpyruvate-dioxygenase
MQVTTFENPMGIDGFEFVEFAAPAGRGQELHEYFRKMGFSAVLKHKQRPITVYRQGDVNFLVNEDPDSFASDFAEKHGPCACGFAIRFKKPGAEVYQTALGNGAEAIAFKPDSKAVSAPVIKGIGDCMLYLVDRYGSAGSIFDGDYEPIAGADLHPVGFGLTFIDHLTHNLYFGNMQQWSDYYERLFNFREIRYFDIKGLKTGLVSKAMTAPDGIVRIPLNESSDPKSQINEYLDAYKGEGIQHIACFTENIYETVEAMRAQGVDFLDTPETYFDVIDQRVPNHGEDVARLAKNKILIDADPETHQRKLLQIFTQNCIGPIFFEIIQRKGNEGFGEGNFTALFESIERDQIRRGVL
>NZ_CP021768.1|WP_042359011.1|4117056_4117551_+|winged-helix-turn-helix-transcriptional-regulator
MSPADPVSTRLRASHVLLDLEQFLPYRLSVLSNRVSGNIAKLYGDRYGLAIPEWRVITILALYPGSSASEVSDRTAMDKVAVSRAVARLLERGFIKRETHGDDRRRSVLALSAAGFEVYETIAPMVIEITRKLMSVLSDEEEQVLEKLILRLAGEGLERMGEGV
>NZ_CP021768.1|WP_087923846.1|4117632_4118772_-|hypothetical-protein
MHSDHAERLPEPASNLAEAGAGEGVTLPPQEALLDDAGTGEETVELAPPRHRLPQIALPDNVVLKGAVQKLVEQKSRLDALAAEGQLAGLLPPEWQGHGVRAIELSTFIQGVLPFLQPGERGETGPARLPVRHVLGDDSRWGLDDVAEPKSLAWYLASDERATAGSKDVAEAYLVGALGLAWMQEGRSRPGFLRAMGQDSLAARVTMLGYPPANELALYSVTAHGQPQIWCVQGRRRMRPLVAPWLSVPLLTAYGVPAPVAWPSSFPPVEAVAELLATARLGRALPEVDLGKVVAKIAEDAASDAWQPVSLLQLNTWSPRWHFFLGTFVGLPSLLLVAAALALPGAVEAATVAASLGFAGGAIAALAVPWIHARRKHLS
>NZ_CP021768.1|WP_087923847.1|4118994_4119594_-|disulfide-bond-formation-protein-DsbD
MRSKLGTAVVVVCAALIGACSQPQPPAAAEPTQPLDTRPTEPPVADPSEPVASGNTPVAADIAAIAGLGAQFDPARDPADDLATAKVEAQRGKKRILLEVGNAACDRCRALDEVVEGNGDLRRFRDAHYVWVKVNASDEQPNAAFFAQYPVMERDYPYLLVLDADGGLLVSQATGELRRGEAFQPARVTAFLKQWAPDR
>NZ_CP021768.1|WP_087923848.1|4119613_4121113_-|MFS-transporter
MSVNATANTPEPALPDFKTTLGHPRPLWMLFMTEFWERFAFYGIRWALVLYIVAQFYNGSAAGEGDASRIYGAYLALVYAAAIFGGYVADRVLGYQRSILTGAIIMAAGLFMISLPQEHIFKLGLATIIVGNGLFKPNISTMVGKLYGLKDERRDSGFTIFYMGINIGAMIAPVLTEYLARKVFGTDAMPSYKVVFIASGVGMLISLVWFYIGRAGLKGIGAPPAGAEGFGRIIMVLAGAVVAIPVAYFLLATGATALAWILGAMFTALAILLLVEGVREGKVQRDRVIAMLIIFAFNVMFWMFFEQAGSSFTFLAENIVNRQFGDWTFPTAWFQSVNSVAIITLAPIIAWIWVAMGRANPSIPRKFGLGLLFNGAAFALLMFALSQMVVDGKIPFWTLFMVYVIQSVGELCLSPIGLSMVTKLAPVRLVGFGMGGWFLSTGIGNNLSGIFAGVVSGEGGMTVESALKGYTFGFWALIGSGVVLFLVAPLINKLMHGVK
>NZ_CP021768.1|WP_087923849.1|4121294_4122170_-|tryptophan-2,3-dioxygenase
MSVDNNQRDLEAGIHTDLQGRLTYGGYLRLDQLLSAQQPLSSPPHHDEMLFIIQHQTSELWLKLLGHELRAAIGFLQRDEVWQCRKVLARSKQVLRQLTEQWSVLETLTPSEYMGFRDVLGPSSGFQSLQYRYIEFLLGNKNAQMLQVFEHDPAGQAQLRIVLEAPSLYEEFLKYLARFGHAVPAVYESHDWTQPHVADDALQPVFERIYQDTDRYWREYALCEDLVDLETAFQLWRFRHMRTVMRVIGFKRGTGGSSGVGFLAKALELTFFPELFQVRTSLQAAPPAERG
>NZ_CP021768.1|WP_087923850.1|4122505_4123588_+|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha
MTVAAEFKIEYLQYLDADGKLVRDDLPASLRDPKVLVPLFKQMLFVRTFDSKSIALQRTGKLGTYAACLGHEAAHVGIGAAMKKDDVFAPSYREYGAMFMRGVRPHDVLMYWGGDERGNDYGGNAAKDFPFCVPISTQCLHAAGAALKFKLNKEPQIAVAVCGDGGSSKTDFYAALNSAGAYKLPLILCIVNNGWAISVPRSAQTGAETLAQKGLAGGLHCLQVDGNDLIAVLAAMEQARERALAGDGGTVLELMTYRLSDHTTADDARRYRDDAEVKDAWQREPMLRLRKYLINAGVWSEEEETAWVAECGTRVDEEVNLYLNTPVQPVEAMFDFLYADPPPDLLAQRAQAIALEKRHG
>NZ_CP021768.1|WP_087924242.1|4123661_4124648_+|alpha-ketoacid-dehydrogenase-subunit-beta
MTTTPITLIEAITQALAWELEHDPSVLVLGEDVGVNGGVFRATAGLQQRFGSERILDTPLDETTIAGLTIGLAAQGMKPVAEAQFDGFMYPMVDHIVCHAARLRYRTRGRLHCPMVLRVPWGGGIRAPEHHSEANEAIFTNVPGLRVVLPSSPQRAYGLLLAAIREPDPVIYMEPKRIYRQYKEVVVNDGEALPLDVCFVLRDGTDVTLVTWGAQVKEALEAADKLAGEGISAEVIDVATLRPLDFATIAESVAKTGRCVIVQEAPKTAGFGAEIAARLAEESIYDLLAPVERVTGYDTHIPLFRLEMKYLPSVERIVAAAKRAVAAG
>NZ_CP021768.1|WP_005411349.1|4124649_4125003_+|hypothetical-protein
MRARLLGAYRSQYPNPLRFHTGQIVEVGVRDEEWPAFAWVRTNDGRAGWAPIAWLQLLDEGRAEALCDYDARELDVESGEMVKLHHEHGGWWWSERANGATGWLPARELELLEENCK

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NZ_CP021768.1	1632522-1632551	0	1.0

1. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to position: 1632522-1632551, mismatch: 0, identity: 1.0

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccatgcggcgtcccatgcggcgtcccgt	Protospacer
******************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_023549	Clavibacter phage CN1A, complete genome	5375-5404	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13708-13737	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13774-13803	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13807-13836	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13708-13737	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13774-13803	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13807-13836	2	0.933
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_023549	Clavibacter phage CN1A, complete genome	5375-5404	2	0.933
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_023549	Clavibacter phage CN1A, complete genome	5411-5440	2	0.933
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13885-13914	2	0.933
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13885-13914	2	0.933
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13642-13671	2	0.933
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_007497	Burkholderia phage Bcep176, complete genome	13642-13671	2	0.933
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_023549	Clavibacter phage CN1A, complete genome	5411-5440	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_023549	Clavibacter phage CN1A, complete genome	5387-5416	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13885-13914	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13675-13704	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13741-13770	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13909-13938	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13885-13914	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13675-13704	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13741-13770	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13909-13938	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13708-13737	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13774-13803	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13807-13836	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13708-13737	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13774-13803	3	0.9
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13807-13836	3	0.9
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_023549	Clavibacter phage CN1A, complete genome	5327-5356	3	0.9
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_023549	Clavibacter phage CN1A, complete genome	5459-5488	3	0.9
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13897-13926	4	0.867
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13897-13926	4	0.867
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	KR011061	Skermania phage SPI1, complete genome	42356-42385	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_023549	Clavibacter phage CN1A, complete genome	5387-5416	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13675-13704	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13741-13770	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13897-13926	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13909-13938	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13675-13704	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13741-13770	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13897-13926	4	0.867
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13909-13938	4	0.867
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13921-13950	4	0.867
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_007497	Burkholderia phage Bcep176, complete genome	13921-13950	4	0.867
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_023549	Clavibacter phage CN1A, complete genome	5363-5392	4	0.867
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	CP054921	Streptomyces sp. NA03103 plasmid unnamed1, complete sequence	86373-86402	4	0.867
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13873-13902	5	0.833
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13873-13902	5	0.833
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13663-13692	5	0.833
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13729-13758	5	0.833
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13663-13692	5	0.833
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13729-13758	5	0.833
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	KR011061	Skermania phage SPI1, complete genome	42356-42385	5	0.833
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_023549	Clavibacter phage CN1A, complete genome	5447-5476	5	0.833
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP023152	Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_1, complete sequence	151685-151714	5	0.833
NZ_CP021768_9	9.1|3170231|29|NZ_CP021768|CRISPRCasFinder	3170231-3170259	29	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1515922-1515950	5	0.828
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_023549	Clavibacter phage CN1A, complete genome	5423-5452	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13696-13725	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13762-13791	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13795-13824	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13828-13857	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13696-13725	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13762-13791	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13795-13824	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NC_007497	Burkholderia phage Bcep176, complete genome	13828-13857	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13696-13725	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13762-13791	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13873-13902	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13696-13725	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13762-13791	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_007497	Burkholderia phage Bcep176, complete genome	13873-13902	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	MT521993	Gordonia phage RedWattleHog, complete genome	117802-117831	6	0.8
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	MN586040	Gordonia phage Stormageddon, complete genome	118749-118778	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13795-13824	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13828-13857	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	DQ203855	Burkholderia cepacia phage Bcep176, complete genome	13873-13902	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_007497	Burkholderia phage Bcep176, complete genome	13795-13824	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_007497	Burkholderia phage Bcep176, complete genome	13828-13857	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_007497	Burkholderia phage Bcep176, complete genome	13873-13902	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	563279-563308	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1186826-1186855	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	788556-788585	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	262786-262815	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	445812-445841	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	312529-312558	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP025613	Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence	554276-554305	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	259129-259158	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP013298	Arthrobacter sp. YC-RL1 plasmid unnamed 1, complete sequence	5399-5428	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP013298	Arthrobacter sp. YC-RL1 plasmid unnamed 1, complete sequence	106591-106620	6	0.8
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	255306-255335	6	0.8
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	MT521993	Gordonia phage RedWattleHog, complete genome	117802-117831	7	0.767
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	MN586040	Gordonia phage Stormageddon, complete genome	118749-118778	7	0.767
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	396714-396743	7	0.767
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NC_023549	Clavibacter phage CN1A, complete genome	5423-5452	7	0.767
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	396714-396743	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	633713-633742	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	376507-376536	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	MH669001	Mycobacterium phage EleanorGeorge, complete genome	38111-38140	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_KR997898	Mycobacterium avium subsp. hominissuis strain 88Br plasmid pMA100, complete sequence	1009-1038	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP024582	Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence	51621-51650	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	50642-50671	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	237158-237187	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	147015-147044	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	392615-392644	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	380594-380623	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_LR134455	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence	220227-220256	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_023286	Streptomyces sp. F12 plasmid pFRL6, complete sequence	7798-7827	7	0.767
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	77117-77146	7	0.767
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	MF580956	Salinibacter virus M8CC-19, complete genome	49916-49945	8	0.733
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	MF580960	Salinibacter virus M31CC-1, partial genome	49913-49942	8	0.733
NZ_CP021768_3	3.2|1632618|30|NZ_CP021768|CRT	1632618-1632647	30	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	963-992	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	452529-452558	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	459359-459388	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_010851	Streptomyces sp. FR1 plasmid pFRL1, complete sequence	12565-12594	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	166701-166730	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	LN997845	Streptomyces reticuli genome assembly TUE45, plasmid : IV	55800-55829	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP027299	Streptomyces sp. SGAir0924 plasmid unnamed_5	111375-111404	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	126188-126217	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP015744	Shinella sp. HZN7 plasmid pShin-08, complete sequence	104535-104564	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	1370904-1370933	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	3928-3957	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	557734-557763	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP039433	Rhodococcus sp. SGAir0479 plasmid unnamed	69339-69368	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	394712-394741	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	564170-564199	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP023779	Nocardia terpenica strain NC_YFY_NT001 plasmid p_NC_YFY_NT001, complete sequence	10429-10458	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_015382	Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence	42569-42598	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_013596	Streptosporangium roseum DSM 43021 plasmid pSROS01, complete sequence	1832-1861	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	166658-166687	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	750743-750772	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	333485-333514	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NC_047865	Aeromonas phage CF7, complete genome	16-45	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	MK967384	Gordonia phage Sidious, complete genome	5709-5738	8	0.733
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	KU963249	Gordonia phage Yeezy, complete genome	5706-5735	8	0.733
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	MF580956	Salinibacter virus M8CC-19, complete genome	49916-49945	9	0.7
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	MF580960	Salinibacter virus M31CC-1, partial genome	49913-49942	9	0.7
NZ_CP021768_3	3.1|1632558|30|NZ_CP021768|CRT	1632558-1632587	30	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	963-992	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1432526-1432555	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	69123-69152	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	MK977705	Gordonia Phage Mollymur, complete genome	11357-11386	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP029340	Streptomyces sp. SM17 plasmid pSM17B, complete sequence	3785-3814	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	NZ_CP029340	Streptomyces sp. SM17 plasmid pSM17B, complete sequence	18480-18509	9	0.7
NZ_CP021768_3	3.4|1632726|30|NZ_CP021768|CRT	1632726-1632755	30	MT024859	Gordonia phage DumpsterDude, complete genome	40167-40196	9	0.7

1. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ccccatgcggcgtcccgtgcggcgtcccgt	Protospacer
 ***************.*************

2. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccgtgcggcgacccatgcggcgtcccgt	Protospacer
****.******* *****************

3. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccgt	Protospacer
**** ******* *****************

4. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccatgcggcggcccctgcggcgtcccgt	Protospacer
************ *** *************

5. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccgtgcggcgacccatgcggcgtcccgt	Protospacer
****.******* *****************

6. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccgt	Protospacer
**** ******* *****************

7. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccatgcggcggcccctgcggcgtcccgt	Protospacer
************ *** *************

8. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 2, identity: 0.933

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ccccatgcggcgtcccgtgcggcgtcccgt	Protospacer
.***************.*************

9. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 2, identity: 0.933

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccatgcggcgtcccatgcggcgggccgt	Protospacer
************************  ****

10. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccctgcggcggcccatgcggcgtcccgt	Protospacer
**** ******* *****************

11. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccctgcggcggcccatgcggcgtcccgt	Protospacer
**** ******* *****************

12. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgcggcggcccatgcggcggcccgc	Protospacer
****************.************.

13. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 2, identity: 0.933

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgcggcggcccatgcggcggcccgc	Protospacer
****************.************.

14. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccatgcggcgtcccatgcggcgggccgt	Protospacer
 ***********************  ****

15. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ggccgtgcggcgccccatgcggcgtcccgt	Protospacer
* **.*******.*****************

16. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccctgcggcggcccatgcggcgtcccgt	Protospacer
 *** ******* *****************

17. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
**** *********** *********** *

18. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
**** *********** *********** *

19. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccct	Protospacer
**** ******* *************** *

20. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcccctgcggcggcccatgcggcgtcccgt	Protospacer
 *** ******* *****************

21. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
**** *********** *********** *

22. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
**** *********** *********** *

23. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccct	Protospacer
**** ******* *************** *

24. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccgtgcggcgacccatgcggcgtcccgt	Protospacer
 ***.******* *****************

25. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccgt	Protospacer
 *** ******* *****************

26. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccatgcggcggcccctgcggcgtcccgt	Protospacer
 *********** *** *************

27. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccgtgcggcgacccatgcggcgtcccgt	Protospacer
 ***.******* *****************

28. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccgt	Protospacer
 *** ******* *****************

29. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 3, identity: 0.9

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccatgcggcggcccctgcggcgtcccgt	Protospacer
 *********** *** *************

30. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 3, identity: 0.9

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gaccgtgcggcggcccgtgcggcggccagc	Protospacer
* ************************* *.

31. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 3, identity: 0.9

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
ggccgtgcggcggcccgtgccacggcccgt	Protospacer
* ****************** .********

32. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
acccatgcggcgtcccctgcggcggcccat	Protospacer
.*************** ******* ***.*

33. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
acccatgcggcgtcccctgcggcggcccat	Protospacer
.*************** ******* ***.*

34. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to KR011061 (Skermania phage SPI1, complete genome) position: , mismatch: 4, identity: 0.867

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccaggcggcgtcccaggcggcgtccagg	Protospacer
***** *********** ********* * 

35. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ggccgtgcggcgccccatgcggcgtcccgt	Protospacer
  **.*******.*****************

36. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
 *** *********** *********** *

37. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
 *** *********** *********** *

38. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
acccatgcggcgtcccctgcggcggcccat	Protospacer
 *************** ******* ***.*

39. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccct	Protospacer
 *** ******* *************** *

40. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
 *** *********** *********** *

41. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgtcccctgcggcgtcccct	Protospacer
 *** *********** *********** *

42. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
acccatgcggcgtcccctgcggcggcccat	Protospacer
 *************** ******* ***.*

43. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccctgcggcgacccatgcggcgtcccct	Protospacer
 *** ******* *************** *

44. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcccgtgcggcggcccctgcggcgacccat	Protospacer
 *************** *******.***.*

45. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 4, identity: 0.867

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcccgtgcggcggcccctgcggcgacccat	Protospacer
 *************** *******.***.*

46. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 4, identity: 0.867

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcccgtgcggcgtcccgtgcggcgccccat	Protospacer
 *********** *********** ***.*

47. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to CP054921 (Streptomyces sp. NA03103 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.867

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcccgttcggcggcccgttcggcggcccgg	Protospacer
 ***** *********** ********** 

48. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

gcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccatgcggcgtcccgtgcgg---cccatgcg	Protospacer
****************.*****   ***.*   

49. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

gcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccatgcggcgtcccgtgcgg---cccatgcg	Protospacer
****************.*****   ***.*   

50. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
tcccctgcggcgtcccctgcgg---cccgtgcg	Protospacer
**** *********** *****   *****   

51. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
tcccctgcggcgtcccctgcgg---cccgtgcg	Protospacer
**** *********** *****   *****   

52. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
tcccctgcggcgtcccctgcgg---cccgtgcg	Protospacer
**** *********** *****   *****   

53. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 5, identity: 0.833

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
tcccctgcggcgtcccctgcgg---cccgtgcg	Protospacer
**** *********** *****   *****   

54. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to KR011061 (Skermania phage SPI1, complete genome) position: , mismatch: 5, identity: 0.833

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
gcccaggcggcgtcccaggcggcgtccagg	Protospacer
 **** *********** ********* * 

55. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 5, identity: 0.833

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgccacggcccgtgcggcgggaagt	Protospacer
******** .***************   **

56. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP023152 (Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_1, complete sequence) position: , mismatch: 5, identity: 0.833

-gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgttcg-gcggcggcccgggcggcggccagt	Protospacer
 *..** *********** ********* **

57. spacer 9.1|3170231|29|NZ_CP021768|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 5, identity: 0.828

-cacacacccggtagcgccgggccatgccc	CRISPR spacer
gcaggc-cccggtagccccgggccaggccc	Protospacer
 ** .* ********* ******** ****

58. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ggaagtacggcgtcccatgcggcgtcccat	Protospacer
*   .*.*********************.*

59. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
.***************.****** .**.*. 

60. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
.***************.****** .**.*. 

61. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
gcccctgcggcgtcccgtgcggc-ccctgcg	Protospacer
**** ***********.****** .**.*. 

62. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccctgcggcgtcccgtgcgg---cccatgcg	Protospacer
**** ***********.*****   ***.*   

63. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
.***************.****** .**.*. 

64. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
.***************.****** .**.*. 

65. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
gcccctgcggcgtcccgtgcggc-ccctgcg	Protospacer
**** ***********.****** .**.*. 

66. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccctgcggcgtcccgtgcgg---cccatgcg	Protospacer
**** ***********.*****   ***.*   

67. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
 ***************.****** .**.*. 

68. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
 ***************.****** .**.*. 

69. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccatgcggcgtcccgtgcgg---cccatgcg	Protospacer
 ***************.*****   ***.*   

70. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
 ***************.****** .**.*. 

71. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt-	CRISPR spacer
acccatgcggcgtcccgtgcggc-ccctgcg	Protospacer
 ***************.****** .**.*. 

72. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt---	CRISPR spacer
gcccatgcggcgtcccgtgcgg---cccatgcg	Protospacer
 ***************.*****   ***.*   

73. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to MT521993 (Gordonia phage RedWattleHog, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tccatcgcggcgtcccatgcggcctcgcgg	Protospacer
***  .***************** ** ** 

74. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to MN586040 (Gordonia phage Stormageddon, complete genome) position: , mismatch: 6, identity: 0.8

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tccatcgcggcgtcccatgcggcctcgcgg	Protospacer
***  .***************** ** ** 

75. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt-	CRISPR spacer
gcccctgcggcgtcccgtgcggc-ccctgcg	Protospacer
**** ******* **********  **.*. 

76. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt---	CRISPR spacer
gcccctgcggcgtcccgt---gcggcccatgcg	Protospacer
**** ******* *****   *******.*   

77. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to DQ203855 (Burkholderia cepacia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt---	CRISPR spacer
gcccatgcggcgtcccgt---gcggcccatgcg	Protospacer
****.******* *****   *******.*   

78. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt-	CRISPR spacer
gcccctgcggcgtcccgtgcggc-ccctgcg	Protospacer
**** ******* **********  **.*. 

79. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt---	CRISPR spacer
gcccctgcggcgtcccgt---gcggcccatgcg	Protospacer
**** ******* *****   *******.*   

80. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_007497 (Burkholderia phage Bcep176, complete genome) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt---	CRISPR spacer
gcccatgcggcgtcccgt---gcggcccatgcg	Protospacer
****.******* *****   *******.*   

81. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgcggcggcccgtccgaagtgctgt	Protospacer
****************** **. *  *.**

82. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggc---ggcccgt	CRISPR spacer
gccggtgcggcggccggtgcggcctgggcg---	Protospacer
*** *********** *******   ***    

83. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggc---ggcccgt	CRISPR spacer
gccggtgcggcggccggtgcggcctgggcg---	Protospacer
*** *********** *******   ***    

84. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggc---ggcccgt	CRISPR spacer
gccggtgcggcggccggtgcggcctgggcg---	Protospacer
*** *********** *******   ***    

85. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggc---ggcccgt	CRISPR spacer
gccggtgcggcggccggtgcggcctgggcg---	Protospacer
*** *********** *******   ***    

86. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cacagtgcggcggccggagcggcggcccgg	Protospacer
  * *********** * *********** 

87. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP025613 (Niveispirillum cyanobacteriorum strain TH16 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgt-gcggcggcccgtgcggcggcccgt	CRISPR spacer
-caggtggcggcggcgcgtgcggcggcccag	Protospacer
 *  ** ******** *************. 

88. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gagcgtgcgggggcccgggcggcggcgtgt	Protospacer
*  ******* ****** ******** .**

89. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP013298 (Arthrobacter sp. YC-RL1 plasmid unnamed 1, complete sequence) position: , mismatch: 6, identity: 0.8

-gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cggtcg-gcggcggcccgtgcggcagcgcgg	Protospacer
 * .** *****************.** ** 

90. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP013298 (Arthrobacter sp. YC-RL1 plasmid unnamed 1, complete sequence) position: , mismatch: 6, identity: 0.8

-gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cggtcg-gcggcggcccgtgcggcagcgcgg	Protospacer
 * .** *****************.** ** 

91. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 6, identity: 0.8

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gccgcggcggcggcccgggcggcggccggc	Protospacer
***   *********** ********* *.

92. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to MT521993 (Gordonia phage RedWattleHog, complete genome) position: , mismatch: 7, identity: 0.767

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tccatcgcggcgtcccatgcggcctcgcgg	Protospacer
 **  .***************** ** ** 

93. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to MN586040 (Gordonia phage Stormageddon, complete genome) position: , mismatch: 7, identity: 0.767

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tccatcgcggcgtcccatgcggcctcgcgg	Protospacer
 **  .***************** ** ** 

94. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 7, identity: 0.767

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ccccatgcggcgttccatgccgcgccgcag	Protospacer
 ************.****** ***.* *. 

95. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NC_023549 (Clavibacter phage CN1A, complete genome) position: , mismatch: 7, identity: 0.767

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ggaagtacggcgtcccatgcggcgtcccat	Protospacer
    .*.*********************.*

96. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 7, identity: 0.767

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
ccccatgcggcgttccatgccgcgccgcag	Protospacer
.************.****** ***.* *. 

97. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gtcacagcggcggccggtgcggcgggccgg	Protospacer
*.*   ********* ********* *** 

98. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgcggcggcctgcgcggcgatgctg	Protospacer
***************.*.******.. *  

99. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to MH669001 (Mycobacterium phage EleanorGeorge, complete genome) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
ctctgtgcggcggccgttgcggcggccgtt	Protospacer
 .*.***********  **********  *

100. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_KR997898 (Mycobacterium avium subsp. hominissuis strain 88Br plasmid pMA100, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgggcggcggcccgggcggcgctgtct	Protospacer
***** *********** ****** . . *

101. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP024582 (Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtgcggcggcctgcgcggcgatgctg	Protospacer
***************.*.******.. *  

102. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tttcgtgccgcggcccgtgctgcggccgat	Protospacer
 ..***** *********** ****** .*

103. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gtgcccgcggcggccggtgcggcggtccgc	Protospacer
*. * .********* *********.***.

104. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gggcgtgcggcggctcgtgcggctgctgct	Protospacer
*  ***********.******** **.  *

105. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
ccgtgggcgacggcccgcgcggcggcccgg	Protospacer
 * .* ***.*******.*********** 

106. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
aacggcgcggcggcccgtgtggcggcctct	Protospacer
. * *.*************.*******. *

107. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_LR134455 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcgggagcggcggccggtgcggcggccacg	Protospacer
**  * ********* ***********   

108. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_023286 (Streptomyces sp. F12 plasmid pFRL6, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gggtgggcggcggcgcgtgcggcgacccgg	Protospacer
*  .* ******** *********.**** 

109. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 7, identity: 0.767

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
acgagtgcggctgcctgtgcggcggcctgg	Protospacer
.*  ******* ***.***********.* 

110. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to MF580956 (Salinibacter virus M8CC-19, complete genome) position: , mismatch: 8, identity: 0.733

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcgtctgcggcgtcccgtgcggcgtcgtac	Protospacer
** . ***********.********* ...

111. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to MF580960 (Salinibacter virus M31CC-1, partial genome) position: , mismatch: 8, identity: 0.733

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcgtctgcggcgtcccgtgcggcgtcgtac	Protospacer
** . ***********.********* ...

112. spacer 3.2|1632618|30|NZ_CP021768|CRT matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 8, identity: 0.733

tcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tggtgtgcggcgtcccaggcagcgtccccg	Protospacer
*  ..************ **.*******  

113. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
agccgtgcggcggccggggcggcggggggc	Protospacer
. ************* * *******   *.

114. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
ggcacgacggcggcccttgcggcggcccta	Protospacer
* *   .********* ***********  

115. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_010851 (Streptomyces sp. FR1 plasmid pFRL1, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cagcgtgcggcggcccgtgccgaggccgag	Protospacer
   ***************** * **** . 

116. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cacagtgcggcggcccgggcggcggcggtc	Protospacer
  * ************* ********   .

117. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to LN997845 (Streptomyces reticuli genome assembly TUE45, plasmid : IV) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gcccgtacggcggcccgtacggcgaagacc	Protospacer
******.***********.*****.    .

118. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP027299 (Streptomyces sp. SGAir0924 plasmid unnamed_5) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cctgaggcggcggccggtgcggccgcccgc	Protospacer
 *. . ********* ******* *****.

119. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgtgcggcggctcgggcggcggtagat	Protospacer
  ************.** *******.  .*

120. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP015744 (Shinella sp. HZN7 plasmid pShin-08, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
ccggctgcggcggcctgggcggcggcccac	Protospacer
 *   **********.* **********..

121. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgcgcggcggcccgggcggcggtgccg	Protospacer
  ***.*********** *******. *  

122. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcaggtgcggcggcccctgcggccgccgcc	Protospacer
 *  ************ ****** ***  .

123. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcaggtgcggcggcccctgcggccgccgcc	Protospacer
 *  ************ ****** ***  .

124. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP039433 (Rhodococcus sp. SGAir0479 plasmid unnamed) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cacggtgcgccggcccgggcggcggccgca	Protospacer
  * ***** ******* *********   

125. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgtgcggcggctcgggcggcggtagat	Protospacer
  ************.** *******.  .*

126. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgtgcggcggctcgggcggcggtagat	Protospacer
  ************.** *******.  .*

127. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP023779 (Nocardia terpenica strain NC_YFY_NT001 plasmid p_NC_YFY_NT001, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gtgcccgcggcggcccgggcggcggccgcc	Protospacer
*. * .*********** *********  .

128. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_015382 (Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tcgcgggcggcggcccgcgcggcggcggca	Protospacer
 * ** ***********.********    

129. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_013596 (Streptosporangium roseum DSM 43021 plasmid pSROS01, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
agacgtccggcggccggtgcggcggcgcag	Protospacer
.  *** ******** ********** *. 

130. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgtgcggcggctcgggcggcggtagat	Protospacer
  ************.** *******.  .*

131. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
atcgcagcggcggccattgcggcggcccgg	Protospacer
..*   *********  ************ 

132. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cgccgtgcggcggctcgggcggcggtagat	Protospacer
  ************.** *******.  .*

133. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NC_047865 (Aeromonas phage CF7, complete genome) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gagcgtttggcggcccgtgcggcggcagca	Protospacer
*  *** .******************    

134. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to MK967384 (Gordonia phage Sidious, complete genome) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cggagggcggcggcccgaacggcggcccga	Protospacer
    * *********** .********** 

135. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to KU963249 (Gordonia phage Yeezy, complete genome) position: , mismatch: 8, identity: 0.733

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
cggagggcggcggcccgaacggcggcccga	Protospacer
    * *********** .********** 

136. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to MF580956 (Salinibacter virus M8CC-19, complete genome) position: , mismatch: 9, identity: 0.7

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcgtctgcggcgtcccgtgcggcgtcgtac	Protospacer
 * . ***********.********* ...

137. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to MF580960 (Salinibacter virus M31CC-1, partial genome) position: , mismatch: 9, identity: 0.7

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tcgtctgcggcgtcccgtgcggcgtcgtac	Protospacer
 * . ***********.********* ...

138. spacer 3.1|1632558|30|NZ_CP021768|CRT matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 9, identity: 0.7

gcccatgcggcgtcccatgcggcgtcccgt	CRISPR spacer
tggtgtgcggcgtcccaggcagcgtccccg	Protospacer
   ..************ **.*******  

139. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tttggtgcggcggaccgtgcggcggggcag	Protospacer
 .. ********* ***********  *. 

140. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tgtttcgcggcgccctgtgcggcggcccgg	Protospacer
  .. .****** **.************* 

141. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to MK977705 (Gordonia Phage Mollymur, complete genome) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
gtgtccgcggcggcctgtgcggcggcctcg	Protospacer
*. . .*********.***********.  

142. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP029340 (Streptomyces sp. SM17 plasmid pSM17B, complete sequence) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tgccgtgcggcggcccgggcgtcgggggag	Protospacer
  *************** *** ***   . 

143. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to NZ_CP029340 (Streptomyces sp. SM17 plasmid pSM17B, complete sequence) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
tgccgtgcggcggcccgggcgtcgggggag	Protospacer
  *************** *** ***   . 

144. spacer 3.4|1632726|30|NZ_CP021768|CRT matches to MT024859 (Gordonia phage DumpsterDude, complete genome) position: , mismatch: 9, identity: 0.7

gcccgtgcggcggcccgtgcggcggcccgt	CRISPR spacer
agtcgtgcggcgacccgtgccgcggcgaag	Protospacer
. .*********.******* *****  . 

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	275964 : 293388	19	Siphoviridae_environmental_samples(23.08%)	head,tail	NA
DBSCAN-SWA_2	620854 : 629235	9	Enterobacteria_phage(42.86%)	NA	NA
DBSCAN-SWA_3	1641260 : 1652169	16	Sulfitobacter_phage(25.0%)	terminase	NA
DBSCAN-SWA_4	3138163 : 3153509	11	Xanthomonas_virus(57.14%)	tail	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP021768|275964:293388|DBSCAN-SWA
GATGCCCCTGCTGACCCTTGAGCAGTGCCGCGCGCACTGCCGTATCGACGGCGACTTTGACGACACCATCCTGGGTGACCTGCTGGCAGCAGCCAGCGACGCGGCCGCAGCCTACCTGGGCCGCGAACTGTACGCCGACCAGACCGGGCTGGACCAGGCACTGGACCAGCTGCCGCAGGACATGGCGGCGGCGGTGACCGGGCATGAAGCCGCGGTTGCCGCCGCCAATGCCGAGACCAATGCGGCCAAGGCCAAGGCCATGCGGGATGTGGCCGATCGCCGCCTGGCCGTGGCGACCGCGCGCAGTGCACGCCTGCTGCTGGGCATGCCCGCCAACGACAGCATCCGTGCAGCGGTGCGCCTGCTGCTGGGCCACCTGTACGCCCACCGCGAAGCCGTGGTTGTCTCTGCGCAGATGCTTGACGACCACGCAGGTACTGCCGCCATTGCAATGGAGCTGCCGTTCGGCGTGGCCGCACTGCTCGATCCGTACCGACCGGCCGCAACGCCATGAACGCCGGCCACTTCAATCGCCGCATCCGCATCGAGCGCCAGAACGGCCAGCTCGATGCCTGGGGGCAGCCGCTGGACGCGTGGCAGCCGGTGGCCGAACTGTGGGCCGCCATCACCGCCGATGCAGCCGACAGCATGCAGCGGCTGACGCTGGAAAGCCGCCTGCCGGCAACGATCCGGCGCCAGCGGTTCCATGTCCGTCTGGGGTCCGCACGACAGGCCGGTATCCACGTCGGCATGCGCATCGTGCATGACGGTCGCGTTTTCAACATCACCGGCGTTGCTCCCGACTTCAGCCGGCGCCAGAGCACGGTGCTGTTCACCGAACAGTCGTCAGGCACTGCCTGAGCGACGCCAACCAGGACACCGCGATGAGTTACGAAGCACAGCTGCACGCGCTGCTGGCCCCGCTGCTGCAGGGCCGGCTGTATCCCGACGTCCCACCGGAACCGGTCATCTACCCGTGTGCCGTCTACCAGCAGATGGGTGGACAGTCCGTGTGGTTCAACGAAGGTTCCACTCCCGAACAGAAGCACGCTCGCGTGCAGCTGACCGTCTGGGCAGACAGTCGTGCCCAGGCCAACACCCTGATCCGGGAGATTGAGGATCAGGTCTGCGCAGGACTGCCGACCGCCGAGTCGTTCGGCGCTGCAATCGGCGTGCACGAGCCGGCACTGCACAAGTACGGCGCGCGGCTCGATTTCGGCCTGTGGTACGTCGACCTGTAAACCGCATCACCCGCGCAACACCCCAGCCCGGCAACCGCCGGGCTTTTTTTTCATCCAACGAGGAAATACACCATGGCACTCAAGCTTCCCAAGGGCACCCAGTTCGGTTTCGCACCGGTCGTCTCCACCGCGATCGCCACCACCGCGATCTCCAAGGCTGCGCCGGCACTGGCCAGCGTTGCCGCCAACAGCGTCGACACCGGCGATGTGGTGGTCATCGAACTGCCGGGCTGGCCGGCCCTGAACAACCGCGCCACCCGCGCCGGTGCTGAAGCCACCGGCAGCGTTGAACTGCTGGGCATCGACACCACCGACACCGTGCTGTTCCCGGGCACCAGCGGCGCCGGCGTGCTGCGCAAGGCCGGCGCCTTCGTCGACCTGGACCAGCAGGGCGACCCGACCACCGCCGGTGGCGAGCAGCAGTACTGGAGCGGCACCCTGCTGGAGGACCCGACCGGCCGCCAGGTGCAGATGCCGACTTTCAAGAACGCCAAGACCATTACCCTGCCGCTGTTCTACGACCCGAAGAAGCCGTGGTATTCGGCGCTGAAGAACGTTGATGCCAAGGGCGAACCGGTGATCCTGCGGGCAAAGCTGGTCGGGGGCGACGTGCTGTACTGGTACGGCTACCTGAGCTACAACGGCGACCCGACCATGGCCGCCAACACCCCGATGGGCACCACCGCGACCTTCACTGCGCTGGCCGATTCCATCCTGGTCGAGGGCGCCTGATGTTCCAGGTAAAGGCGCCGGAAAGCTTCAAGAGCACCCTGACCATCGTCGGTCACGGTCGCGAGCAGAAGCTCAACCTGACCTACCGGCACCTGTCGGTAGCCGACTACGCCGGCCTGCTGGAGCGGTTGGCCGAGGAGGAGCTGAGCGTGGCCCAGGCGATCCTGGACATCGTGGTGGAGTGGGATGCCGATGTGGCGCTGGATACCGCCGGCGTCGAGCTGGCCCTGCAGCAGCAAGCCGGCCTGGATGGCGCCATCATCGGTGGCTACACCCAGGCGCTGCAGGTCGCGCGCAAGGGAAACTGATCGAGGCGGTGGGGGCCCTGTACTGGCGGGCCCCCACCGAGGCCGAGCTGCAGCAGCTCGGTCTGAAGGCACGGCATTTCCCGCCACCGCAGGTCACGCTGTGGCCGGAGTGCGTACTTCCCATCGAGGTTTTCTCACGGGTTTCCACCCAGTGGCGCGTTGGCGCAGGTGGCCCGATCGGGCTGGATTACAACGTGGTCTACCGGGAACTGGAGCGCGAAGCGCTCGCACCAGACAAACGCGATGAGGTGATGGCGGGAATCCGCATCATCGAGCGTGCGGCGCTGGACCACATGCAGCAGCACTAAGCCGCCATCGACACCGGTCGATGGCTCCATCATGGCTCCGCCACTGCGCGGGGCCTTTCTTCATGTCAGGAGAATTTCATGAGCGATTCAACGCTCAGTGACTCGGCTGCCGCTGTCAAAGTCAGCGCGATCGTGGCCTCCGCCGCTCAAGCGGCAACGCAGGGTGTGAGCCAGCTCGCCAATGCTGCACAGCAGCTGCCCGTCCAGCTCACCCAGGCCACTGTACTGCACCAGGCACTGAACACTGTCATGAGCAGCAGTGTTTCCATGATGAACACACTGGTGCAGCAACTGACCGCCACGGCAATGAAAGCGGCTGCCACGCAGGCAGCGATCGAGAGCCGACAGGAAAACCCTCTGGGCACCGGTGCGCTGGGTGTCGCACCGTTTGCTTCGATCAACGTACCCGACTTCGTTGAAAAGCAGCGGAAGTACGGTAGTGGAATGCTCAACGGCGTGCCCCTGCTTCCGCCCGAGAAGAAAGAAACAACTGAGAAAGAAGACAAGAAGACGGGCTTTGCCGGTGCAGGAAAAGGCGTGGAGGCCGCCTTTGACAGCTATCTCAGCAAGGCTGAAGACACTGCGACAACGACGAAGGCGGCCTTCGACAAGGCTTTCGCCGGCGCCGAAACAGCGCTCTACAAGTTCGTGACTACAGGAAAGTCCGGCTTTCGCGAGCTCACCAAGGCCATCATCGCCGATCTCGAACGCATCGCTCTTCAGCAGGCGATCGTATGGGGGGTGAAAACCATTGCCAGCTTCTTTGGTGGCGCCAGCGCAGCGCCCAGTTCCAGCTTCGCAAGCGGCTTCGGCAACAACACCGGCTGGCTGAGCAGCGGCAACATGACGCCCAATGCGCTTGGCGGCGTCTACGCATCGCCCAGCTTGTCGGCCTATTCCGGCGGCATCTACAACACCCCGCAGCTGTTCGCCTTCGCCAAGGGTGCCGGCGTATTCGGCGAAGCGGGACCGGAAGCGATCATGCCGCTGCAGCGCGGACCGGACGGCCGCCTGGGTGTGGCCGCGCACGGTGGCGGCGGTGGCGGCGGAGTGGGTGTAAGCATCCGCATCGACAACAACGGTGGCAAGGAAGTCACCACCAACGAAAGCATGCTGCAGCAGTTCGGCAACGAGATCGGCCAGTTCGTGGAACGCAAGTACCGCGAACTGCAGAGTCGTGACCTGAAGGCAGGTGGTGTGCTCAGCAGGAGTGCCATGTAATGACCGATACCTTCACCTGGCCGGCAACCAGCCAGAGCACCGGGACCACCACCGCCGCCGTGAAGCGCGCGAAGTTCGGTGATGGCTATGCGCAGGCCGCCGCTGATGGCCTGAACGCCACCTCGCGCAGTTACCAGCTGCAGTTCGTAGGCAACCGCAGGACGATCAACGAAATCGTTGCTTTCCTGGATGGTCATGCCGGCCGCAGCTTCCTGTGGAAGGGGCCACTGGGGCAGGGGCTGTACATGTGTGACTCCTACACCGACAGCCATCTCGGTGGACAGGTCTCGACCATCACCGCCACGTTCGAGCAGACCTTCCAGGCGTAGGCATGAGCATGGATCTTCAACGGATCGACCTGGATACCATCCAGCCCAACGGAAAGCGTGGAGAGACCCAACGGCCCGCCTTCACCAAGATCAACCAGAACTTTCAGGATGTTGCGTTGGCGCTGGAGGGAATCCCCGGTGCCATCGCAGACTCTGTCTCGGGAAAGAACCGCTTGATCAACGGGAATTTCGACTTCTGGCAGCGTGGGGACAACTTCACCGCTGCTGCGGCCTACTGTGCGGACAGATTCTTTGCACAGCAGGGAGGGATGGATGGCGCAGGCATATTCAAATCACCCGTTGCTCCGGGCGATGCGAACTTCCCGAAAAGCCTGTTCACGTTGGCCGCCAATTGCAACGGGAACCACAACGCTGCCGGACACCATTTCCTGTTCGAGCAGCGTGTGGAAAGTGTGCGGACCTTTGCCGCATCAGAGAGCACGCTATCCTTCCTGGTCTACAACGCAGGCACTGCAGGGAGAAAGATCGCAGTCGAATTCCTGCAGCGCTTCGGAACAGGCGGAAGCCCCACTGTCACGGGGATACAGCCGGAAGTGTTTACGCTCGCACAGGGCCTGAACCGGATCAGCAAGACCGTCAGTCTTCCTTCCATCTACGGTAAGACGCTTGGCAGTGGCGATGATTCGGTCATCTGTGCGGTATGGCTCTCGGCAGGCAGTGACTTCAATGCGCGCACAGGAGGGCTCGGCGCGCAGGCAGGCCAGTTGTACTTCGGCGAAATGCAGTGGGAAGCCGGCGCACGCGCGACCCGCTTCGAGTGGAGATCACCGGCCCACGAGCTTGCGCTGTGTCAGCGCTACTACCAGAAGTCCTTCCCTGTTACAGAAGTTCCCAACAGCAGGAGCAGCTCCGCCGTGCACCGGAACGCAGTGGCCTTCAACAGTGGCACCTGCCGCGTTGTCGCAGAGTTCAAAGGCACGATGCGCAGCACGCCACAGCTGCAGTTCCACGCAGGCGGGGAAGGTGGTGACATCGGATCGCCGAGCTTCTGGAGGTACTACGACGCCGCTGGCGGAACATGGCGCGCGGGAACCCTGACCAATGTAGTCATGGCAACGAGCCAGGCGTTCATGGCGGACGTGGGTGGAGCAGGTTTCCTGGTAAGCGGCTCTGTTCTGCTGGCAGGCCACTACACCGCCGATGCCGAACTCTGAGTGCATTCCTACATCTGCGGGACCGGTCGGGAAGCCGTGAGACCCGCCCGTTGACGGAATGAAAGTACTCGAACTCCGATCGGCCGCCCCCGATTCACCTCGTTCAAGGAGCCACTAATGGCAAGAAAGATCATCGACCTCGATTCCGTTCAACCGAACGGAAAGCGGGGTGAAACACAGCGCCCGGCGTTCACCAAGATCAACGAGAATTTCGCCGAGGTCTACGACGCCTTGACCGATGTCGCGAAGATTCCGGAGACCGTGGGGAATGCCATCACCGAGCGCGTTCCGGGAAGGAATCTGCTTATCAATGGTGGCCTTCAGTTCTGGCAACGTCGCACGTCCGGTCGCGTTGGCCAGGGATCAGGTACGCTGGGTGCGGAGACATTCTTCGCCGACCGCTTCACGAACTCGGCGCTGGTCTGCAACCACGATGTGCAGCGTGTAGCTTACGACGGGCAGGCTGGATTTCCGGAAGATACCCGGTCGATTCTGGTCTGCACCGTATCCGAGGCCATCGCCAGAAGTGGCGCCTGGATGGGGCAGAAGATCGAGGGCGTCCGCAGTGCAAGTGGAGACATCACGATCTCGGTGTGGGCGAACTCTGATGCGCCAGGTCGCAGTGTGGGCGTGCGTGTCATCCAGGATTTCGGGACAGGTGGCTCACCCTCGCCGCAGGTGACAGTGGAAGCCGGCGTGCTCAAGCTGGAGGCGACCGCCAAGCGCCACAGCATCACGGTGAAGCTGCCGAGTACCCGGGGCAAGGTGCTTGGCAGCAATGGCAACGACCATCTCTACGTGGTGTTCGACCTGTGCGGTACCGGCCAGGGGGGCGAGCTGGTGGCGCAGAACGGATCGTTCGGCTTCACACAGTTCCAGGTCGAAGCCGGGCGCGCAGCGACGCGCTTTGAGTGGCGACCGCCGGGCGTGGAACTGGCGTTGTGCCAGCGCTACTACGAGAAGAGCTACAACCTCGACATCGTGCCCAATACCGCGCACAACGAAGGGCGCGAAGCCTTCTCGATCAACTCACCGGGAGTGGCGCACTACCAGAGTGTGCGATTCCATGCACCGAAGCGTACCCATCCTTACGTGATGATCATCTCGGCCGACAACATCCAGCAGGACGGACATATCGCGGAAGACAACATCTCCCGCGTTCCCTGCCTGGTCAACTATGCCTCGCCTTCCGGCTACGAAGTGAGCTGGACCAACAATCCAGGTCGCTGGGGCGGGTGGTGGCATTGGTGGGCCGATGCCGAGCTGTGATGGCGCGTGCCCGGGACTTACAGGACGACAGCAATGACGAGAAAAATCATCGACCTCGATTCCGTTCAACCGAACGGAATGCGGGGTGAAACCCAGCGCCCGGCGTTCACCAAGATCAACGACAACTTCGCCGAAGTGTATGGGGCGCTGGATGGCGTGACCGCGATCGGGAAGCGTGTGGATTCACTGGAAAGCGCTTTGCAGAGCGTGGTTCCAGGCAGGAACCGCCTGATCAACGGCAACTTCGATTTCTGGCAGCGGGGCACCACCGGCACCACCCAGGGGGGAGAGATCTATGTAGCCGATCGCTGGACCGTGGCAGCGCTGGGCTGCACGCATACCGTCAATCGCGGCGGCAATCTGCCAGCTGGCGGTGCCGCTCCGGAATCGCGCCGTTTCCTCAACAGCGTTGTCTCCAAGACCAGTGCAGGTAGCAGCGCCTACGTCGCACAGAAGGTCGAGAGCGCGGCGACGCTGTCCGACGGCGACGTGACGGTTTCCGGCTTCGCCTATGGCCCGCCAGGAAAACGCATCGGCGTTCGTCTCATCCAGCACTTTGGCACCGGTGGTTCGCCGTCCGCCGCAGTCAGCGTGGAGCTGGGAACCGTAGCGGTCACCGCCACGTCCTGGACCTATTTCCAGCTCAGTGCGCGACTGCCATCGGTGAAGGGGAAGACGCTGGGCAGCAATGCCGACAGCGATTTCCTGTGGCTGGTGGTGGATCTGTGCGCGGATGCCTATGGCGGTGTCATCTCCGGGCAGAACGGAGAGTTCGGTATTGCGATGATGCAGCTGGAGCGCGGCAACCGGGCAACGGCATTCGACCTGCGCCCGCTGGCCCACGAGCTGCAGCTGTGCCAGCGCTACTACGAAAAGTCCTATGACAATGACGTCGTTCCTGGAACTCCGACCAACAGCGGTCGTTACAGTTGGGGCAACTCGGCTGCGAGCGGCGCAACCAGCTACCTGTCGGTGCCATTCAAGACGTGCAAGCGAGTGACGCCGGTGATTGTCGTCAGGCCCAACAACAATGTGGTCGAGCCCGGATATGTCAATCAGGACGACAGCAGCCGAACGCCCGCATCGGTTCCCACGATCGCGACGAACGTCTTCGAAGTGGCCTGGGGCAATTCTCCCGGGCGTTGGGGTGGCTGGTTCCACTGGACGGCGGATGCAGAGATTTACTGAGTATCAGGTATGGCGTTCCGCCGTCTTTTTCAGGCGTGGCAACGACCTGTCCCTGGGCTTTGCTGATTCGGAATGGAAGGCTAAATGAGCAGAAAGATAATCGACCTCGATACCGTTCAGGCGAACGGTAAGCGGGGTGAAACACAGCGCCCGGCATTCACCAAGATCAACGACAACTTCGCCGAAGTGTATGGCGGGTTGGATGCCGTGCAGACTGCGGTGGATGGGTTGGATGGCCGAATGACTGGCCGCAACTGCCTGATCAACGGCGACTTCCGCCTTTGGCAGCGTGGTGCAGTGTTTCCTGCATCCGTGGGCACTCGCTACATCGCTGACCGCTGGCAAGCCAATGCCACCGGCACCAAGCTGGCCGTCACACGCGAGGATGTGCCTGCAGGCGGCGGCCAGGGAGGGCGCCTGCTGGCCGGATCACGCCACCTGCTCCGGCTGGATGTGCAGAGCGTGGCCAGTGCCGGCAATATGGCACTGGTCCAACAGCGTATCGAGGACGTCCGGACCCTGGCCGGGCGCACTGTGACCATCAGCTTCAAGGCACGCGCCTCGGTGGATGACTTCCGCATCGGGGTGGAGCTGCAGCAGTCTTACGGAACGGGCGGGTCCACCGCGCGCGACAGCATCGGCGCCTCGGTCGTACTCGATACCCTGTGGCGATGGCACCAGGTCACCGTGGATGTTCCCGGCCTTGCCGGCAGGACGCTGGGCCCGGACAGCTACCTGCAACTGAGCTTCTGGCTGGATGCCGGTGCCGATTTCGGCGGGCGGGCGTTCGCCGCCGGGCAGAAGAGCGGCAGCGTGCAACTGGCCGAAGTGCAGATCGAAGAAGGCGACACCGCCACCGACTTCGATCGCCGGCCTGAAGCACTGGAGCTGTTGCTGTGCCAGCGCTACTACGAGACGTTGGATGTGAACCGGATCCTGGGCATCACCTACACCGCCAACGGTGACACGCGCGCGTGCATTCCGTTCAAGGTACGCAAGCGCGTGGCGCCCAGGGTCACCTCGCCCTCTGCCGCGCTCAACCTGGTCGGCTTCGGCTCCGAAGGTAGCCTCATCAACTTCAACGGTGGCGATCCGGGCTGGCAGTCCACCGTGGACGCGGCCGTGCTGTCCACGATGTCCAACAACATGCAGCAGTGGGGTGCGGTGGTGGTGTGGTCGACCACCTCACAGGTGCTGGTGCAGGCCGATGCGGAGCTCTGAGCCATGACAATCACGCCTCCGCAGGCGTCAAAGCACGCCTGCTTCACGACCACTACGTCGCTGCGCCCGGGCCACCACGTCATCGTACCGCGCGGCCAGGAGCGGTATCCCGTACCACCCCCTCTTCCCATTGCCGCACAGGAGCACACCCCATGATCACCGCCGATGCCCAGCAGCTTGAGCCGGGTGGCCGCATCACCGTCTACGAGCTCGACGCCAGCAGTTTCGGCGCCGACAAGCTGTTCTTCCACGCACACCTGCAGAGCGGCCTCGTCTGGTGGCAGGGCCAGGAATATGGCCCCTGGCCGATCGAGGCCAGCGGCTTCGAACGTACCAGCGACCAGCCACCGAATCCGCGCCTGCGCGTGAGCAACATCGATGGCCGCATCACCGCCATGTGCCTGTTGTTCGACGACCTGGTCGGGGCCCGCATCATCCGCCGGCAGACGCTGGCCAAGTACCTGGATGCCGCCAACTTCGAGGAAGGCAATCCCAGCGCGGATCCTGCCGAGCATTTCCCCGACGAAGTCTGGTTCATCGAGCGCAAGATCGGCGAAGACAAGCAGATGGTCGAGTTCGAGCTGACCACCGCGATCGATCTCAATGGCCAGCAGTTGCCGGGCAGGCAGATCATCGCCGGCATGTGTGGCTGGCTGGTGCGTGGCGGCTATCGCGGCGCGTACTGCGGCTACAACGGTCCGGCGGTGGCCGACAGCGACGACGTCGCTACCGACGACCCGGCACGTGATCAATGCGGTGGCCGGGTACGCAGCTGCAAGCTGCGCTTCGGCCAGGACAAGCCGCTGCCCTATGGCGGCTTCCCCGCCGCGGGTCTGTTGCGCTCCTGATCGATCCCTTCCCGATTCCACTTTCCAGGCCCGCCCGCGCGGGCCTTTTTCATGGGTGAAACATGCAACCGACAACCCTGCAGGCCATCCAGGCGCACGCCGTGGCCGAGTACCCGCGCGAATGCTGCGGGCTGATCGTGGCCGTTGAAGGCCACGAACGCTATCTTCCTTGCCGCAACGTGGCCGCCATGCCCAGCGAGCATTTCCGTCTGCCGGCCGAGGACTATGCCGTGGCCGAGGACAAGGGCGAGGTGCTGGCCCTGGTGCACAGCCACCCCGATGCCGCCGCGACGCCGTCCGACGCCGATCGGGTCATGTGCGAGCGCAGCGGGCTGACCTGGCACATCGTCAGCGTCGGCCAGGTAACCGGCGAGCCACCGCTGTGCGGTGATCTGCAGACCCTGCATCCCTCTGGCTACATGGCACCGTTGGTCGGTCGTCAGTTCGCCCATGGTGTGCTGGACTGCTACAGCCTGGTCCGCGATTTCCACGCACGCGAACTGGGCATCCGGCTGTCCGAGTACGAACGCCAGGATGACTGGTGGAGCCATGGCCAGGACCTGTACAGCCTTGAACGGCTGCACGCCGAGGGCTTCGACCTGATCGAGGGCGAACCGCAGCGGGGCGACATGATCCTGATGCAGATCCGCTCGCCGGTTACCAACCACGCAGGCATCTACCTCGGCGACGGGCAGATGCTGCATCACCTGCATGGCCGCCTGTCCGAGACCGTGCCCTACGGCGGCATGTGGGCCGAGCGCACCCGTTGCATCGTCCGCCATCGCGAGGTGCGCCATGACTGACCGTCTTCGTACGATCCGCCTGTACGGCAAGCTGGGTGCCCGCTTCGGGCGCAGGTTCCGGCTGGCGGTGAACAGCCCGGCCGAGGCCGTGCATGCGCTATGCACGATGCTGCCGGGGTTCCAGCAGTACCTGATGGGTGCCAAAGCCAAGGGCATGGAATTTGCCGTGTTCAATGGCCGGCAGAACCTGTCGCGGGATCAGCTGCACGATCCGCCAGGGCAGGATGACATCCGCATCGCGCCGGTGATGGTGGGTAGCAAGCGAGGAGGCGTGCTGCAGACGATCATGGGCGTTGTACTGATTGTCATCGGAGCGGTCATGAATGCGTACGCACCAGGGAGTGGCGCGGGAGTCATGACGTCGGGCATTGGCATGGTCGCTGGCGGGGTCGTGCAGATGCTCTCCCCCCAGCCAAAAGGCCTGGGCGCCAAAGACACACCCGAAAACGCGCCCAGCTACAGCATGAACGGCACCGTCAACACGCAGGCGCAGGGCAACCCCGTACCGGTCGCTTATGGCGGCCATGACAGCAAGGGCATGTTCATCGGCTCGGCCGTGATCAGCGGCGGCATCCTGGCGGAGGACCAGTTTTGAACCAGATCACTCATTCCACGCCGCGCACGCGCGGTGCAGCCGCGCCCGTACTGGTGGGCGCCAAGAAGGGCGCGAGCAACGCCCGAACCCCGGTCGAAACCGCCGACAGCCTGCACTCGATGGCGGTGGCCCGCATCATCGACCTCGCCAGCGAAGGCGAGATCCGCGGCCTGGTCGCCGGCAAGCAGTCGATCTACCTGGACCAGGTGCCGATCGAGAATCCGGACGGCACGCTGAACTTCTCCGGCGTGGACGTGCAGACGCGTTCCGGCACCCAGGACCAGGAGCACATCAGCGGCTTCCCGTCCATCGAGAACGAAGTCGGTGTCAATGTCGAGCTGCGCAGCGATGCGCCGGTGGTACGCACCGTATCCGGTGCCGACCTGTCGGCCGTCCGTATCCGCTTCGCGGTGCCGGCGTTGCAGAAAACCAACACCGAGAACGGTGACACCGAAGGCTACCGGATCATGTATGCGGTGGATCTTTCCACCGATGGTGGCCCGTTCAGCACGGTGCTGACCGATGCCTTCAGTGGCAAGACCACCAGCCAGTACGAGCGCAGCCGCCGCATCGATCTGCCTGCCGGCAGCCAGTGGCAGGTGCGCATCCGCCGGCTGACCGCCAACGCCAACAGCAGCACCATCGCCGATACCATCAACGTGCTGTCGATGACCGAGATCATCGATGCCAAGCTGCGCTATCCGAACTGTGCGCTGGCGGCGGTGCAGGTCGACGCCAGCCAATTCCAGAACATCCCCACCCGGTCCTACCAGCTGTGGGGGCGCATCGTGCGCATCCCCTCCAACTACGATCCGCTCAGCCGTCTCTACAGCGGCGTGTGGGACGGTACCTTCAAGAGCGGGTGGACCAACAACCCGGCCTGGGTGTTCTTCGACATCGTCACCAACGATCGCTTCGGCCTGGGTCATCGTGTTCCGCTGGACTGGGTGGACAAGTGGCGGCTGTACCAGATCGCGCGCTACTGCGATGAACTGGTCAGCGATGGCCAGGGCGGCAAGGAGCCGCGCTTCACCTGCAGCCTGTATCTGCAGACCCGCGCCGAGGCCTATCGCGTGCTGCAGGACATCGCCACCATGTTCCGCGGCATCAGCTTCTATGCGGCGGGGCAGGTGATGGCCTCGGCCGACATGCCCAAGGACCCGGTGCTGACCTACAGCCAGGCCAACGTCATCGAAGGCCGCTTCCACTATGCCGGCAGCAGCCGCACGGCGCGGCACACGGTGGCCCTGGTGTCGTGGATCGATCCGGATGACTTCGGCCGGCAGAAGGTCGAAGTGGTACAGCACCTGCCCGGCGTGGCCCGCTACGGCATCAACCAGACCGAAGTGACGGCGGTGGGCTGCCACTCGCGTTCGCAGGCGCAGCGCGTGGGCAACCACATTCTGCATACCGAGATGCTGGAAACGGAAACCATCAGCTTCTCGGTGGGCCTGGACGCGCTGGGCTGCATGCCTGGTGACGTGATCCAGGTGGCCGACCCGAACCGCGCCGGCCGCCGCAATGCGGGACGCATCCGCAGTGCGGGTACGCGCAGCCTGGTGCTGGATCGCGTGCCGGAACAGGTCGCTGCCGGTGACACCCTGCGCGCCACCCTGCCCAGCGGGCAGACCGAAGCACGCACGGTGCAGTCGGTGGACGGCGAGACAGTCACGGTCACCGCGCCGTGGTCGGCGGTGCCGGTGGCGCAGTCGGTCTGGGCGCTGGAATCGCCTGAGCTGGCCCTGCAGCACTATCGCGTGCTGTCGGTCAGCGAAGGCGAGGATCTGACCTATCAGATCACCGCGCTCAAGCACGTGCCGGGCAAGTACGCCGCCATCGACGACGGCACGCGCCTGGAGCAGCCGCCGATCAGCATCATTCCGCCCAGCGTGCAGCCGGCACCGGCCAACGTGCGGATGGCCTCGCATGTGGTGGTGGACCAGGGCATCGCCACCTCCGTGCTCACCATCGAGTGGGATGCCGCAGACAAGGCGATCGGCTATGACGTGGAATGGCGCCGTGGTGATCTCAACTGGGTCCGCGCCGGTCGCGTCGGGACGCAGAGCCTGGAGGTGCGGGGCGTTTACGCGGGCGAGTATCTGGCCCGGGTACGCGCGGTCAATGCGCTGGGCGCGGTATCGCAGCCGACGCTCAGTGTGCTCACCACCATTGAAGGCAAGACGACGCCGCCGCCGGCATTGACCTCGCTGACCGCGCGCAGCCGCGTGTTCGGCATCGAGCTGGCCTGGCAGTTCCCGGCAGGCGCCACGGATACCGAGCGCACGGAGCTCTGGTACAGCACCAGCCCGGATCGCTCGGCCGCCATCAAGCTCGGCGACTTCGCCTATCCACAGTCGCGGCACCAGATGAATGGTCTCGCAGCTGGCGCACGCTTCTGGTTCTGGGGGCGCCTGGTTGATCGCAGCGGCAACGTGGGTCCGTGGCATCCGGTGGAGGCGGGTGTTCTGGGCGAGTCCAGCAGCAACCCATCGGACTACGATGCCTATTTCGCCGGCCGCATCAACGAAAGCGCGCTGGGCCAACAGCTGAAGGGCAAGATCGAGCGCGTCACCGAAGTGCTGCCGCTGGTCTGGGATGCCGCGGCAACCTACACCCCGGGCCAGACCGTCATCCACGATGGCCGGATCTGGAGCTGGCAGGGCACTGCCGCAGGCAATGAAACGCCGCCGGGCAGCCACTGGAAGAACATCGGCGACGCCGTCGCCGAGGCGGGCGCCATCGTCGGCCGTGTTGATCAGCTGGAACTGGACGTTACCGACGTCGATGGCAAGGTGGCCGCGCAGGGGCAGAAGGTCGATGGCCTGTTCGCGCAGGTCAGCGACCACACCGCCGGTGAGGAGGACTACAACGTCGGCGAGAACGACGTCAGCGCCGGTGCCATCACCGTCTACAGCGTGATGGCCGAGAAGGACGCGGCACTGGCCAGGCGTGTGGACACGGTCGAAGCCTCCATCGAGGGTGTTCCAGGCAAGATCGAAGGGGTCAGTGCCGCGGTCCAGCAGGTCTCGCAGGCCGTGGTGAACCTGGATGGCAAGGTCAGCGCAACCTATACGGTCAAGGCGCAGATCAGCAGTGCCGGGCAGATCTACATGGCCGGCATGGGTCTGGGCGTGGAGCAGCAGCCGGATGGCAGCTACCAGAGCCAGATCCTGATGCAGGCCGATCGCTTCGCGCTGTTCAACACCAACAGTGGCCAAGTCAGCGCGCCCTTCGTGGTGCAGGGCGGGCAGACCTTCATCAGCCAGGCACTGATCGGCAACGGCTGGATCCAGAACGCGATGATCGGCGATGTGATCCAGTCCAACGCGGTCGGTGCCGGCGGGCAGCCTCGCTGGAGGCTCGACAAGAACGGCACGCTGACGATGAACGGCCCCGAGAACGGCGGCCGCCTGACCATCAATGACAGTGTCATCCACGTTTACGACAGCAACGGCCGCGTCCGCGTCCGCATGGGGATCTGGTAATGGCAACCGGTATGCAGATATTCGGCCCGGACGGGCAGATGTGGTTCGACACCAATGATCGTGCCGGCAAGGTGATGGGTGAGATGCACGTCAGCACCCGAGACAGCATCTATGTGGGCATGGCGGGCATGGGGCAGCCATTCGCGATCCTGCCAAGCACCTTATGGGACAGCTGGCAGGACATGAATGGGAACCAGTTCTCCGCGCCAAACATGGCATCCATGTCCTTCAACAAACCAGGCGCCGCCGAAGGCGACTACCTCACACTCAACTTCACGTTCATGACGACGACCAACCCCAACGCCTATGTCTTCTACGGGAGTTTCTGATGACCGTCGGCCTTGAAGTCACCAACGACAGCGGTATCCCCGTTCTGGTCAACGCACGCGCCCTTGCCTTCTTCGCGGCAGGCAAGGGGGTGGAGACCATCGGTAGCAACACTTCGCCGTTGGGCCAGAACGGTTCGGTCGGCCTGCCGGCGCAGAGCGTGCCCTACCTGGTGTTCATCCGCTGCAATGGCGGCTCCACGCGGATCTCCACCGGCACTGCAGGTTTCAGCTGGAACATGGCCCAGGGCACCACCAGTTTTGAATGGTGGGCATGGGGACATGCGGTTCCCAGCAACAACACCGGCATGCAGGTCTACAACGCCGACGGTTCGCTGCAGTGGGACATGAGCAGCCGTCCACTGCGCATGGCGGGCCTGGTCGATAAGACCGGTGCCCGGCCACCACTCCCCAGCGAGATGTCCAACGAGAACATCCTCACCGGTGACCTGATCAACGGCCCAGGCGAAAATCTTGCCTACCTGCTGTCAGACATCGGTCTCTGCCACGATGTCTACGCGATGCCCAGCGGCAACCCCACCATCCGTACCAACATGCGCTATGCGGCAGCCATCAGTACGCCGAATGCATCGCAGATGCGTGTCAACTTCACCCGGCAAGCTGCCAATCGCCAGCGTTCCCTCAGTGGAGCGTCCTACCAGACGTTCGCTTCGCGCCTGCCAAGCTTCGTCCTTGCGGCTTACACCTACTGAGTGGGGGTTGCCGGCCCGGGCGGCCATTTGAGCCGCCCGGGCCCTTCCCGTAGACTGCGCCCCTCCTACGCTCCTCGACGACGCACTGCAGTGATCACGCCACCCTGACCCTTGCCGCACATCGGCAGCCGGCCCGCCCGGCTCAGGAACCCGTGTCTTTCCACTGCAGCGCCATGCGGCCACGCCCGCGTGCGCGCGGAGTTTTCCCATGCAAACGTCCTACCCCCTGCGCCAGCAATGGCTCGGCAACATCCGTGGTGATCTGTTGTCCGGCATGGTCGTCGCCCTGGCCCTGATTCCCGAGGCCATCGCCTTCTCGCTCATCGCCGGCGTCGACCCCAAGGTCGGCCTGTATGCCGCGTTCTCCATTGCGGTGGTCACCGCCATCGCCGGTGGCCGCCCCGGCATGATCTCCGCCGCCACCGGCGCGATGGCACTGGTGATGGTCGACCTGGTCAAGGACCACGGCCTTCAGTACCTGTTCGCCGCCAGCATCCTGGCTGGCCTGCTGCAGGTGCTGGCCGGCGTGTTCAAGCTTGGCTCGCTGATGCGCTTCGTTTCGCGCTCGGTCATCACCGGCTTCGTCAACGCGTTGGCGATCCTGATCTTCCTGGCGCAGATGCCGGAACTGATCGGCCGTGGTCCCACGGTCTACGTGCTGTGTGCCGCCGCCCTGGCGATCATCTACCTGCTGCCGCGCCTCACCCGTGCGGTGCCGTCACCGCTGGTGGCGATCGTGGTGCTTACAGCCGTGGTGATCGGTTTCGATGTGGACGTGCGCAGTGTTGGCGACATGGGCCAGCTGCCCGACAGCCTGCCGCAGTTCCTCATCCCCGATGTGCCGCTCACCTGGGAGACCCTGCGCATCCTGCTGCCGGTGTCGGCCACGCTGGCCGTGGTCGGCCTGCTCGAATCGATGATGACCCTGCAGATCGTCGAGGACATCACCGAAACGCCCAGCGAGCGCAACCGCGAATGCGTCGGCCAGGGCGTGGCCAACACGGTCACCGGTTTTCTCGGCGGCATGGCCGGCTGCGCGATGATTGGGCAGTCGGTCATCAACGTGACGTCCGGTGGCCGCGGCCGCCTGTCCTGCCTGGTGGCGGGCGTGCTGCTGCTGGTGCTGGTGGTGTACGGCAGCGACCTGGTGCGGCAGATCCCGATGGCCGCGCTGGTGGCGGTGATGATCATGGTCAGCATCGGCACGTTCAGCTGGCGCTCGCTGCGCGACCTGCGCACGCACCCGCGCAGCTCTTCGGCCGTGATGCTGCTGACCGTGGTGGTCACCGTGGCCACCCACGACCTGGCCAAGGGCGTGCTCAGTGGCGTGCTGCTGTCGGCGCTGTTCTTCGCGCGCAAGGTCGGCCGCATGTTGGATGTGCAGCGCGAAGATGCCGGAGACACGCAGGCCTACCGCGTACGTGGGCAGGTGTTCTTTGCCTCGGCCGGCCAGCTGGGCGCCGCGTTCGACTACCAGCATGTGGCACCAAAGGTGCAGATCGACCTGCGTGACGCCCACCTGTGGGACCTCACTGCGGTGGCCGCGCTGGAACGCGCTCAGGAAAAGCTGGCCGCGCATGGGGCGGAGGTGACGGTGGTGGGCCTGAATGCGGCCAGCCGTACGTTGATCGAACAGGTGGGTGGGCGCGGCGGCGGGCACTGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP021768|275964:293388|276473_276824_+|WP_087921202.1|head,tail|DBSCAN-SWA
MNAGHFNRRIRIERQNGQLDAWGQPLDAWQPVAELWAAITADAADSMQRLTLESRLPATIRRQRFHVRLGSARQAGIHVGMRIVHDGRVFNITGVAPDFSRRQSTVLFTEQSSGTA
>NZ_CP021768|275964:293388|287197_290686_+|WP_087921216.1|DBSCAN-SWA
MNQITHSTPRTRGAAAPVLVGAKKGASNARTPVETADSLHSMAVARIIDLASEGEIRGLVAGKQSIYLDQVPIENPDGTLNFSGVDVQTRSGTQDQEHISGFPSIENEVGVNVELRSDAPVVRTVSGADLSAVRIRFAVPALQKTNTENGDTEGYRIMYAVDLSTDGGPFSTVLTDAFSGKTTSQYERSRRIDLPAGSQWQVRIRRLTANANSSTIADTINVLSMTEIIDAKLRYPNCALAAVQVDASQFQNIPTRSYQLWGRIVRIPSNYDPLSRLYSGVWDGTFKSGWTNNPAWVFFDIVTNDRFGLGHRVPLDWVDKWRLYQIARYCDELVSDGQGGKEPRFTCSLYLQTRAEAYRVLQDIATMFRGISFYAAGQVMASADMPKDPVLTYSQANVIEGRFHYAGSSRTARHTVALVSWIDPDDFGRQKVEVVQHLPGVARYGINQTEVTAVGCHSRSQAQRVGNHILHTEMLETETISFSVGLDALGCMPGDVIQVADPNRAGRRNAGRIRSAGTRSLVLDRVPEQVAAGDTLRATLPSGQTEARTVQSVDGETVTVTAPWSAVPVAQSVWALESPELALQHYRVLSVSEGEDLTYQITALKHVPGKYAAIDDGTRLEQPPISIIPPSVQPAPANVRMASHVVVDQGIATSVLTIEWDAADKAIGYDVEWRRGDLNWVRAGRVGTQSLEVRGVYAGEYLARVRAVNALGAVSQPTLSVLTTIEGKTTPPPALTSLTARSRVFGIELAWQFPAGATDTERTELWYSTSPDRSAAIKLGDFAYPQSRHQMNGLAAGARFWFWGRLVDRSGNVGPWHPVEAGVLGESSSNPSDYDAYFAGRINESALGQQLKGKIERVTEVLPLVWDAAATYTPGQTVIHDGRIWSWQGTAAGNETPPGSHWKNIGDAVAEAGAIVGRVDQLELDVTDVDGKVAAQGQKVDGLFAQVSDHTAGEEDYNVGENDVSAGAITVYSVMAEKDAALARRVDTVEASIEGVPGKIEGVSAAVQQVSQAVVNLDGKVSATYTVKAQISSAGQIYMAGMGLGVEQQPDGSYQSQILMQADRFALFNTNSGQVSAPFVVQGGQTFISQALIGNGWIQNAMIGDVIQSNAVGAGGQPRWRLDKNGTLTMNGPENGGRLTINDSVIHVYDSNGRVRVRMGIW
>NZ_CP021768|275964:293388|285107_285803_+|WP_087921213.1|tail|DBSCAN-SWA
MITADAQQLEPGGRITVYELDASSFGADKLFFHAHLQSGLVWWQGQEYGPWPIEASGFERTSDQPPNPRLRVSNIDGRITAMCLLFDDLVGARIIRRQTLAKYLDAANFEEGNPSADPAEHFPDEVWFIERKIGEDKQMVEFELTTAIDLNGQQLPGRQIIAGMCGWLVRGGYRGAYCGYNGPAVADSDDVATDDPARDQCGGRVRSCKLRFGQDKPLPYGGFPAAGLLRS
>NZ_CP021768|275964:293388|277276_277936_+|WP_087921204.1|tail|DBSCAN-SWA
MALKLPKGTQFGFAPVVSTAIATTAISKAAPALASVAANSVDTGDVVVIELPGWPALNNRATRAGAEATGSVELLGIDTTDTVLFPGTSGAGVLRKAGAFVDLDQQGDPTTAGGEQQYWSGTLLEDPTGRQVQMPTFKNAKTITLPLFYDPKKPWYSALKNVDAKGEPVILRAKLVGGDVLYWYGYLSYNGDPTMAANTPMGTTATFTALADSILVEGA
>NZ_CP021768|275964:293388|278252_278552_+|WP_087921206.1|DBSCAN-SWA
MGALYWRAPTEAELQQLGLKARHFPPPQVTLWPECVLPIEVFSRVSTQWRVGAGGPIGLDYNVVYRELEREALAPDKRDEVMAGIRIIERAALDHMQQH
>NZ_CP021768|275964:293388|291933_293388_+|WP_087921219.1|DBSCAN-SWA
MQTSYPLRQQWLGNIRGDLLSGMVVALALIPEAIAFSLIAGVDPKVGLYAAFSIAVVTAIAGGRPGMISAATGAMALVMVDLVKDHGLQYLFAASILAGLLQVLAGVFKLGSLMRFVSRSVITGFVNALAILIFLAQMPELIGRGPTVYVLCAAALAIIYLLPRLTRAVPSPLVAIVVLTAVVIGFDVDVRSVGDMGQLPDSLPQFLIPDVPLTWETLRILLPVSATLAVVGLLESMMTLQIVEDITETPSERNRECVGQGVANTVTGFLGGMAGCAMIGQSVINVTSGGRGRLSCLVAGVLLLVLVVYGSDLVRQIPMAALVAVMIMVSIGTFSWRSLRDLRTHPRSSSAVMLLTVVVTVATHDLAKGVLSGVLLSALFFARKVGRMLDVQREDAGDTQAYRVRGQVFFASAGQLGAAFDYQHVAPKVQIDLRDAHLWDLTAVAALERAQEKLAAHGAEVTVVGLNAASRTLIEQVGGRGGGH
>NZ_CP021768|275964:293388|283818_284955_+|WP_087921212.1|DBSCAN-SWA
MSRKIIDLDTVQANGKRGETQRPAFTKINDNFAEVYGGLDAVQTAVDGLDGRMTGRNCLINGDFRLWQRGAVFPASVGTRYIADRWQANATGTKLAVTREDVPAGGGQGGRLLAGSRHLLRLDVQSVASAGNMALVQQRIEDVRTLAGRTVTISFKARASVDDFRIGVELQQSYGTGGSTARDSIGASVVLDTLWRWHQVTVDVPGLAGRTLGPDSYLQLSFWLDAGADFGGRAFAAGQKSGSVQLAEVQIEEGDTATDFDRRPEALELLLCQRYYETLDVNRILGITYTANGDTRACIPFKVRKRVAPRVTSPSAALNLVGFGSEGSLINFNGGDPGWQSTVDAAVLSTMSNNMQQWGAVVVWSTTSQVLVQADAEL
>NZ_CP021768|275964:293388|275964_276477_+|WP_087921201.1|head,tail|DBSCAN-SWA
MPLLTLEQCRAHCRIDGDFDDTILGDLLAAASDAAAAYLGRELYADQTGLDQALDQLPQDMAAAVTGHEAAVAAANAETNAAKAKAMRDVADRRLAVATARSARLLLGMPANDSIRAAVRLLLGHLYAHREAVVVSAQMLDDHAGTAAIAMELPFGVAALLDPYRPAATP
>NZ_CP021768|275964:293388|285865_286606_+|WP_087921214.1|DBSCAN-SWA
MQPTTLQAIQAHAVAEYPRECCGLIVAVEGHERYLPCRNVAAMPSEHFRLPAEDYAVAEDKGEVLALVHSHPDAAATPSDADRVMCERSGLTWHIVSVGQVTGEPPLCGDLQTLHPSGYMAPLVGRQFAHGVLDCYSLVRDFHARELGIRLSEYERQDDWWSHGQDLYSLERLHAEGFDLIEGEPQRGDMILMQIRSPVTNHAGIYLGDGQMLHHLHGRLSETVPYGGMWAERTRCIVRHREVRHD
>NZ_CP021768|275964:293388|286598_287201_+|WP_087921215.1|tail|DBSCAN-SWA
MTDRLRTIRLYGKLGARFGRRFRLAVNSPAEAVHALCTMLPGFQQYLMGAKAKGMEFAVFNGRQNLSRDQLHDPPGQDDIRIAPVMVGSKRGGVLQTIMGVVLIVIGAVMNAYAPGSGAGVMTSGIGMVAGGVVQMLSPQPKGLGAKDTPENAPSYSMNGTVNTQAQGNPVPVAYGGHDSKGMFIGSAVISGGILAEDQF
>NZ_CP021768|275964:293388|282579_283734_+|WP_157721482.1|DBSCAN-SWA
MTRKIIDLDSVQPNGMRGETQRPAFTKINDNFAEVYGALDGVTAIGKRVDSLESALQSVVPGRNRLINGNFDFWQRGTTGTTQGGEIYVADRWTVAALGCTHTVNRGGNLPAGGAAPESRRFLNSVVSKTSAGSSAYVAQKVESAATLSDGDVTVSGFAYGPPGKRIGVRLIQHFGTGGSPSAAVSVELGTVAVTATSWTYFQLSARLPSVKGKTLGSNADSDFLWLVVDLCADAYGGVISGQNGEFGIAMMQLERGNRATAFDLRPLAHELQLCQRYYEKSYDNDVVPGTPTNSGRYSWGNSAASGATSYLSVPFKTCKRVTPVIVVRPNNNVVEPGYVNQDDSSRTPASVPTIATNVFEVAWGNSPGRWGGWFHWTADAEIY
>NZ_CP021768|275964:293388|277935_278244_+|WP_087921205.1|DBSCAN-SWA
MFQVKAPESFKSTLTIVGHGREQKLNLTYRHLSVADYAGLLERLAEEELSVAQAILDIVVEWDADVALDTAGVELALQQQAGLDGAIIGGYTQALQVARKGN
>NZ_CP021768|275964:293388|278630_279773_+|WP_087921207.1|tail|DBSCAN-SWA
MSDSTLSDSAAAVKVSAIVASAAQAATQGVSQLANAAQQLPVQLTQATVLHQALNTVMSSSVSMMNTLVQQLTATAMKAAATQAAIESRQENPLGTGALGVAPFASINVPDFVEKQRKYGSGMLNGVPLLPPEKKETTEKEDKKTGFAGAGKGVEAAFDSYLSKAEDTATTTKAAFDKAFAGAETALYKFVTTGKSGFRELTKAIIADLERIALQQAIVWGVKTIASFFGGASAAPSSSFASGFGNNTGWLSSGNMTPNALGGVYASPSLSAYSGGIYNTPQLFAFAKGAGVFGEAGPEAIMPLQRGPDGRLGVAAHGGGGGGGVGVSIRIDNNGGKEVTTNESMLQQFGNEIGQFVERKYRELQSRDLKAGGVLSRSAM
>NZ_CP021768|275964:293388|280104_281277_+|WP_087921209.1|DBSCAN-SWA
MSMDLQRIDLDTIQPNGKRGETQRPAFTKINQNFQDVALALEGIPGAIADSVSGKNRLINGNFDFWQRGDNFTAAAAYCADRFFAQQGGMDGAGIFKSPVAPGDANFPKSLFTLAANCNGNHNAAGHHFLFEQRVESVRTFAASESTLSFLVYNAGTAGRKIAVEFLQRFGTGGSPTVTGIQPEVFTLAQGLNRISKTVSLPSIYGKTLGSGDDSVICAVWLSAGSDFNARTGGLGAQAGQLYFGEMQWEAGARATRFEWRSPAHELALCQRYYQKSFPVTEVPNSRSSSAVHRNAVAFNSGTCRVVAEFKGTMRSTPQLQFHAGGEGGDIGSPSFWRYYDAAGGTWRAGTLTNVVMATSQAFMADVGGAGFLVSGSVLLAGHYTADAEL
>NZ_CP021768|275964:293388|279772_280102_+|WP_087921208.1|tail|DBSCAN-SWA
MTDTFTWPATSQSTGTTTAAVKRAKFGDGYAQAAADGLNATSRSYQLQFVGNRRTINEIVAFLDGHAGRSFLWKGPLGQGLYMCDSYTDSHLGGQVSTITATFEQTFQA
>NZ_CP021768|275964:293388|290685_291015_+|WP_087921217.1|DBSCAN-SWA
MATGMQIFGPDGQMWFDTNDRAGKVMGEMHVSTRDSIYVGMAGMGQPFAILPSTLWDSWQDMNGNQFSAPNMASMSFNKPGAAEGDYLTLNFTFMTTTNPNAYVFYGSF
>NZ_CP021768|275964:293388|276847_277204_+|WP_087921203.1|DBSCAN-SWA
MSYEAQLHALLAPLLQGRLYPDVPPEPVIYPCAVYQQMGGQSVWFNEGSTPEQKHARVQLTVWADSRAQANTLIREIEDQVCAGLPTAESFGAAIGVHEPALHKYGARLDFGLWYVDL
>NZ_CP021768|275964:293388|291014_291725_+|WP_087921218.1|DBSCAN-SWA
MTVGLEVTNDSGIPVLVNARALAFFAAGKGVETIGSNTSPLGQNGSVGLPAQSVPYLVFIRCNGGSTRISTGTAGFSWNMAQGTTSFEWWAWGHAVPSNNTGMQVYNADGSLQWDMSSRPLRMAGLVDKTGARPPLPSEMSNENILTGDLINGPGENLAYLLSDIGLCHDVYAMPSGNPTIRTNMRYAAAISTPNASQMRVNFTRQAANRQRSLSGASYQTFASRLPSFVLAAYTY
>NZ_CP021768|275964:293388|281394_282546_+|WP_087921210.1|DBSCAN-SWA
MARKIIDLDSVQPNGKRGETQRPAFTKINENFAEVYDALTDVAKIPETVGNAITERVPGRNLLINGGLQFWQRRTSGRVGQGSGTLGAETFFADRFTNSALVCNHDVQRVAYDGQAGFPEDTRSILVCTVSEAIARSGAWMGQKIEGVRSASGDITISVWANSDAPGRSVGVRVIQDFGTGGSPSPQVTVEAGVLKLEATAKRHSITVKLPSTRGKVLGSNGNDHLYVVFDLCGTGQGGELVAQNGSFGFTQFQVEAGRAATRFEWRPPGVELALCQRYYEKSYNLDIVPNTAHNEGREAFSINSPGVAHYQSVRFHAPKRTHPYVMIISADNIQQDGHIAEDNISRVPCLVNYASPSGYEVSWTNNPGRWGGWWHWWADAEL

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087921201.1|275964_276477_+|head,tail	phage gp6-like head-tail connector protein	NA	NA	NA	NA
WP_087921202.1|276473_276824_+|head,tail	head-tail adaptor protein	NA	NA	NA	NA
WP_087921203.1|276847_277204_+	DUF3168 domain-containing protein	NA	NA	NA	NA
WP_087921204.1|277276_277936_+|tail	phage tail protein	C4ML12	Xanthomonas_virus	1.4e-64	57.5
WP_087921205.1|277935_278244_+	hypothetical protein	NA	NA	NA	NA
WP_087921206.1|278252_278552_+	hypothetical protein	A0A2H4JBP7	uncultured_Caudovirales_phage	1.3e-06	30.2
WP_087921207.1|278630_279773_+|tail	phage tail tape measure protein	K7P6X5	Enterobacteria_phage	2.6e-18	30.1
WP_087921208.1|279772_280102_+|tail	phage tail protein	C7BGC9	Burkholderia_phage	4.2e-22	55.5
WP_087921209.1|280104_281277_+	hypothetical protein	A0A0H4IPB2	Stenotrophomonas_phage	2.1e-31	31.5
WP_087921210.1|281394_282546_+	hypothetical protein	Q2PGC1	Xanthomonas_oryzae_phage	6.0e-31	38.7
WP_157721482.1|282579_283734_+	hypothetical protein	Q2PGC3	Xanthomonas_phage	1.1e-29	39.8
WP_087921212.1|283818_284955_+	hypothetical protein	A0A0H4IPB2	Stenotrophomonas_phage	3.1e-72	49.8
WP_087921213.1|285107_285803_+|tail	phage minor tail protein L	A0A2R3UA90	Siphoviridae_environmental_samples	2.1e-92	66.7
WP_087921214.1|285865_286606_+	C40 family peptidase	A0A2R3UAR4	Siphoviridae_environmental_samples	1.2e-80	58.4
WP_087921215.1|286598_287201_+|tail	tail assembly protein	W0LI27	Edwardsiella_phage	5.3e-47	51.0
WP_087921216.1|287197_290686_+	host specificity protein J	A0A2R3UA88	Siphoviridae_environmental_samples	0.0e+00	58.5
WP_087921217.1|290685_291015_+	hypothetical protein	NA	NA	NA	NA
WP_087921218.1|291014_291725_+	hypothetical protein	NA	NA	NA	NA
WP_087921219.1|291933_293388_+	SulP family inorganic anion transporter	A0A2H4J153	uncultured_Caudovirales_phage	6.8e-157	65.0

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP021768|620854:629235|DBSCAN-SWA
AGTGCCCACATGGCTTGTCACCGGCGGTGCCGGATTCATTGGCGGTAACTTCGTTCTCGAGGCCGTGGCGCGCGGCGTCAAGGTCGTCAATCTCGACGCCCTGACCTATGCCGGCAACCTGAAGACCCTGTCCAGCCTGGACGGCAACCCGAACCACGTGTTCGTGCAGGGTGACATCGGCGACAGCGCCTTGGTCACCCGCCTGCTGGCCAAACACCAGCCGGACGCGGTGCTCAATTTCGCCGCCGAGAGCCACGTCGACCGTTCCATCGATGGCCCGGGTGCGTTCATCCAGACCAATGTGGTGGGCACCCTGGGCCTGCTGGAAGCGGTGCGCGACTACTGGAAGGCGTTGCCGGCCGAGCAGGGCGCAGCATTCCGCTTCCTGCATGTGTCCACCGACGAGGTGTACGGCACCCTCGGTGAGACCGGGAAGTTCAGCGAAACGACCCAGTACGCCCCCAATTCCCCGTACTCGGCGTCGAAGGCCGCATCGGACCACCTGGTGCGTGCATTCCACCACACCTACGGGCTGCCGGTGCTCACCACCAACTGCTCCAACAACTATGGCCCGTACCATTTCCCCGAAAAGCTGATCCCGCTGGTGATCGCCAAGGCCCTGGCCGGCGAACCGCTGCCGGTCTACGGCGATGGCAAGCAGGTGCGCGACTGGCTGTTCGTGTCCGACCACTGCGAAGCGATCCGCACCGTGCTGGCCAAGGGCCAGGTCGGCGAGACCTACAACGTCGGCGGCAATTCGGAAAAGCAGAACATTGAAGTGGTGCAGGCGATCTGCGCACTGCTGGACCAGCGCCGCCCCCGCGCGGACGGCCAGCCGCGCAGCAGCCAGATCACCTACGTCACCGACCGACCCGGCCATGACCGCCGCTATGCGATCGATGCCTCGAAGCTGAAGAACGACCTGGGCTGGGAACCGGCTTACACGTTCGAGCAGGGCATCGCCTACACCGTCGACTGGTACCTGGACAACCAGGACTGGGTCAATGGCGTGCTCGACGGCAGCTACCGCCTGCAGCGCATCGGCACCACGGCCTGAATCCAGGAGACACCATGACCCAGCGCAAGGGCATCATCCTCGCCGGTGGTTCCGGCACCCGGCTGTATCCGATCACCAAGGGCGTCAGCAAGCAGCTTCTGCCGGTGTACGACAAGCCGATGATCTACTACCCGCTCAGCGTGCTGATGCTGGCGGGTATCCGTGAGGTCCTGATCATCAACACGCCGCATGAGCAGGCGTTGTTCCAGCAGTTGCTGGGCGACGGTTCGCAGTGGGGCATGGACATCCAATACGCAGTGCAGCCGAGTCCGGATGGCCTGGCCCAGGCTTACCTGATCGGCCGCGACTTCGTGGCGGGCAAGCCGAGCTGCCTGGTACTGGGCGACAACATCTTCCACGGCCATGGCCTGCGCGAAGTGCTCAAGCGCGCCGACGAACGCGTGCACGGCTCGACCGTGTTCGGCTACTGGGTCAATGATCCGGAACGTTACGGCGTGGCCGAGTTCGACCAGAGCGGCAAGGTGATCGACCTGGTCGAGAAACCGGAAAAGCCGCGCTCCAATTATGCGGTGACCGGTTTGTACTTCTATGACGGCAACGCCAGCGATTACGCAGCCGAACTGAAGCCGTCGCCGCGGGGCGAACTGGAGATCACTGATCTCAACAAGCGCTACCTGGCCGAAGGCAACCTGCACCTGGAGGCGCTCGGTCGTGGCTATGCGTGGCTGGACACCGGTACCCACCAGTCGCTGCTGGAGGCATCCAACTTCATCGAGACCATCCAGACCCGTCAGGGCCTGCAGGTCTGCTGTCCCGAGGAAATCGCATTCGGCAAGGGCTGGATCAGTGCCGAGCAGCTGGAAGCATTGGCTGCGCCGCTGATCAAGAACGGCTATGGCCAGTACCTGCATACGCTCGCCCAGCGCGGAGTCGTTCCGTGAAGGTGATCGAGACTTCACTGCCGGGGTGCCGGGTGATCGAACCGGCGGTATTCGGTGACGAGCGCGGGTTCTTCTTCGAGACCTGGAATGCCGAGCGCTTTACCGCACTGGGGTTGCCTGATCGCTTCGTGCAGAGCAATGTCTCATCGTCGGCCAAGGGCGTGCTGCGTGGCCTGCATTTCCAGTGGCCGCGGCCGCAGGGCAAGCTGGTCAGCGTGCTGGAAGGCGAGGTCTACGACGTCGCCGTCGACATCCGCCGCGGCTCGCCTACCTTCGGTCGTTGGGAGGCGGTGGTACTGAGTGCTGAAAACAGGAAGCAGTTCTGGATTCCTGAAGGCTTCGCCCATGGATTCGCGGTGCTGTCCGAGCGCGCACTGTTCAGCTACCTGTGCACGGATGTCTACGTCAAGGAAACCGACGCCGGCATCCGCTGGAACGATGCCGACATCGCAATTGACTGGCCGATCAGTGCACCGACCTTGTCGGCGAAAGACGAGAACGCACCGTTCCTGAAGGACATTGCCGAGGACCGCCTGCCGGTCTACACCCCATGACGGTGCTGGTGTTCGGCGGCAACGGCCAGGTCGGCCAGGAGCTGCTGCGCGCGCTGGCCCCGCTGGGGGCAGTGGTTGCCACCACGCGCAGCGGCACGCTGCCGGATGGCAGTGCCTGCGAAACCGCCGACTTCAGCCAGCCTGACAGCCTGCCAGCCCTGCTGGATCGTCTGCAGCCGTCGGTGGTGGTCAATGCGGCCGCTTACACCGCCGTGGACCGTGCCGAGCAGGACGTGGAGGCCGCGTTCGCGGCCAACGCGCAGGCACCGGGCGTGATCGCGCGCTGGTGTGCGGCGCACGGCGTGCCGTTCGTGCATTACTCCACCGATTACGTGTTCGATGGCCAGGGCAGCGCGCCCTACCGCGAAGACGAGCCGACCGCACCGCTGGGCGTGTATGGCACCAGCAAGCGCGACGGTGAAGACGCGGTGCGTGCGGCCGGCGGTCGCCATCTGATCTTCCGCACGGCGTGGGTCTACGCCTCGCACGGCGCCAACTTCCTGCGCACCATGCTGCGGGTGGGCGCGGAGCGCGAGCAGCTGCGCGTGGTGGCCGACCAGATCGGTACACCGACGCCGGCCGCGTTGATCGCCGATGTCACCGCGCAGGCGCTGCAGCATCCGGGCCAGTTGTCTGGTACCTGGCACCTGACGGCCAGTGGCCAGACCAGCTGGCATGGCTTTGCCGAGGCGATCTTCGCCGAGGCGTTGGCCACCGGCGCGTTGGCCAAGGTGCCGACGGTCGAGGCGATTCCCAGTTCCGAGTATCCGACCCCGGCCAAGCGCCCGGCCTGGTCGGTGCTGGACAATCGCAAGCTGCAGCAGGATTTCAGCATCGTGCTGCCGGCCTGGCAGGACGGCCTGAAGCGGGTGATGGCGGAGATTGCCTGACCCGGTAGGCGGCGTGCCGACCAGCGGTCGGCACCCACCCCGATCCGCCGTCGGCAGCCACCAGCGGGCGCTGGGTCAGCTGCGCCCGTAGGTATCCTCGAACCGCACGATGTCATCCTCACCCAGATAGCTGCCGGACTGCACTTCGATCAGTTCCAGCGGCAGTTTGCCGGGGTTGCGCAGGCGATGGGTCACGCCCAGCGGAATGTAGGTGCTCTGGTTCTCGCTGAGCAGGATCACCTCGTCACCACGGGTCACTTCGGCGGTGCCGCTGACCACGATCCAGTGCTCGGCGCGATGGTGATGCATCTGCAGGCTCAGCGTGCCGCCGGGCTTGACCGTGATCCGCTTGACCTGGAAGCGCTCGCCGTTGTCGATCGAATCGTAGGCGCCCCACGGGCGATAGACCTTGCGATGCCAGGTGGCCTCGCTGCGGCCCTCGGCCTTGAGCTGTGCGACCACCGTCTTGACCTCCTGCATGCGGTCGGCCTTGCCGACCAGCACCGCGTCGTCGGTTTCCACCACGATCACATCGTCCAGCCCGACCAGCGCCACCAGGCGCTGTGCGTAGGCATAGGTGTTGCGGCAGTCGATGGCGATCACGTCGCCCTGGTGGGCATTGCCATCGCCGTCCTGCTGCGAGACATCGCGCAGCGCGGTCCACGAGCCGACATCGTTCCAGCCTGCATCCAGTGGAATCACCACGGCATCGGCGGTCTTCTCCATCACCGCATAGTCGATGGAATCGGACGGAACGGCGGTGAAGGCGTCCTTGTCCAGGCGGGTGAAGTCGGCATCGCGACGCGCCTGCTGCCAAGCTTGGCGGCTGCCGACGAGCATGGCGGGCTGGAAGCGTTCCAGCTCCTGCAGGTAGCGCGAGGCCTTGAACAGGAACATGCCACTGTTCCAGTAGTACTGGCCGCTGCTGACGTAGTCGGTGGCGGTGTCCAGGTCGGGCTTCTCGACGAAGCGCTCGACCGCGCGCAGGCCCTGGCCATCGGCGGCCTTGATATAGCCGTAGCCGGTTTCCGGGCCGGTCGGCACGATGCCGAAGGTGACCAGCTTGCCGGCTTCGGCGGCACCGGCGGCGGCCTGAACCGCTGCGCGGAACGCCGCCTCGTCGGTGATCACGTGGTCGGAGGGCAGCACCAGCAGCAGGGCGTCGGCGCCGTCGCGGGTGGCTTCCAGCGCGGCCACCGCGATCGCCGGGGCCGTGTTGCGGCCGACCGGCTCAAGGATGATCGCGGCCGGCTCGGCGCCAACCTGCTGCAGCTGCTCGGCGGCGACGAAACGGTGCTCTTCGTTGGCGATCACCAGCGGCCCACGCGCGGCGATCGGCGCAACGCGCTTCCAGGTGGCCTGCAGCATCGTCAGTTCGCCCGCCAATGGCAGGAACTGCTTCGGATACGCCTCGCGCGAAAGCGGCCACAGGCGGGTACCGGATCCACCGGACAGGATGACGGGCTGGATGCTGCTCATGCGTTCCTCGGTTACTGCTGGATGAGGCGGGAAATGTCGTCGGTGCGCGCCTGCATCAGCGCGGCATCGCCCCGGGCTTCAACATTCAGGCGCAGCAGTGGCTCGGTGTTGGAGCTGCGCAGGTTGAAGCGCCAGTCGCCGAAGTCGGCGCTGATGCCGTCGGTGTGATCCAGCGCCGGCGACTGCGCGGCGAAGTGTTCCATCACGCGCGCGACCGCAGCCTTGGCATCGGCAACCTTGAAGTTGATCTCGCCACTGCACGGGTAGGCGGCCATGCGGTCTTCGACCCAGTCGGCCAGCGAACGCCCGCTTTCGGAAACCAGCTGGGCAATCAGCAGCCACGGGATCATGCCGGAGTCTGCATAGGCGAACTCGCGGAAGTAGTGGTGGGCGCTCATCTCGCCGCCGTACACCGCGTCTTCGGCGCGCATCTTTTCCTTGATGAAGGCGTGGCCGCTCTTGCACTGTACCGGCACACCGCCGGCCTGCTCGACCATGTCCACGGTGTTCCAGACCAGGCGCGGGTCATGCACGACCTTGCCGCCCGGGTTGCGCGCCAGGATCGCCTTGGCCAGCAGGCCGACCAGGTAGTAGCCCTCGATGAAGCGGCCGGTATGGTCGAAGAAGAAGCAACGGTCGAAGTCGCCATCCCAGGCGATGCCGAAATCGGCGCCGTGCTCGCGCACCGCGTCGGCGGTGGCGGCGCGGTTCTCCGGCAGCAGCGGGTTGGGAATGCCGTTGGGGAAGCTGCCGTCCGGTTCGTGGCAGATGCGGATGAACTCGAACGGCAGGTGCGGTGCCAGCAGGTCGACGATGGCACCGGCACCGCCGTTGCCGGCGTTGACCACCAGCTTCAGCGGGCGCAGCTTGGGGGCATCGACGTAGCTCAGCAGATGCTGGATGTACGCGCTCTTGTCATGCTGGGCGCTCTGCCCGGCGCGCGGCGGCTGCGCCTCGGACGTATCGGCGGCGACCGCATCGGAAATCGCGAACAGGCCGGTATCCGAACTGATCGGGCGCGCGTTCTCCTTGACCAGCTTCATGCCGTTGTAGTCCATCGGGTTGTGGCTGGCGGTGACCATCACGCCGCCGGCCGCGCCCAGATGGTCGGTCTGGAAATAGACCTCTTCCGTGCCGCACAGGCCGATGTCGATCACCTCGCGCCCGGTGCCGCGCAGGCCTGCGGCCAAGGCGTCCTGCAGCGCAGGGCTGGTCAGGCGCACGTCGTGGCCCAGTACCACCGGGCCTGGTGCAAGCTGCGCCGCCAGTGCCACGCCGATGCGGCGCGCCAGCTCTTCGTTCAGTTCTTCCGGCACGCGGCCGCGGATGTCATAGGCCTTGAAGGCGGGCAGGGGCATCGATCGGATCCTTGGGGAGCTCAGCCCAAGATTGTAGTCCCAGTCCTGTATGGGAATCGTTTCCATGCCGCAACGCCACGTGACCGGTGGGTGCGCTGGCCTAGAATGGGCGGATTACATCAACGAGGTGAGGGCGTAGATGAGCAACCCGGCAACGACCGGCGGAAAGCGCGGCAAGCGCTTCGCCAGTGCGGCGGAGGCCCTGCAGGGGGTGGTCGCCGATGGCCAGACCCTGGCCGTGGGCGGCTTTGGCCTGTGTGGCATTCCCGAGGCGCTGATCGCTGCGCTGCGCGACAGCGGCGTCAAGGGCCTGACCGTGATCTCCAACAATGCCGGCGTCGATGGCTTCGGCCTCGGCCAGCTGCTGGAAACGCGGCAGATCAAGAAGATGATTTCGTCCTACGTGGGCGAGAACAAGGAATTCGAGCGGCAGTTCCTGGCCGGCGAGCTGGAACTGGAGTTCAACCCGCAGGGCACCCTGGCCGAGCGCCTGCGCGCCGGCGGTGCCGGTATCCCGGCGTTCTTCACCGCCACCGGCTACGGCACGGTGGTGGCCGAGGGCAAGGAAACCCGCGAGTTCGACGGCAAGCACTACGTGATGGAAACCGCACTGCGCGCCGACGTGGCGCTGGTCAAGGCCTGGACGGCCGACGAGGCCGGCAACCTGGTGTTCCGCAAGACCGCACGCAACTTCAACCCGGCCTGTGCGATGGCCGGCAAGGTCTGCATCGTGGAAGTGGAAGAGGTGGTGCCGGTCGGCGCCATCGACCCGGACCAGGTGCACCTGCCGGGTATCTATGTGCACCGCATCGTGCACAACGCGCATCCTGAGAAGCGAATCGAACAGCGCACCATCCGCGCGGAGGGCAACTGACATGGCGTGGACCCGTGACGAGATGGCGGCACGCGCCGCCCAGGAACTGACCGATGGCGCCTACGTGAACCTGGGCATCGGCCTGCCGACGCTGGTGGCCAACCACATTCCCGACGGCGTGGATGTGTGGCTGCAGTCGGAGAACGGCCTGCTCGGCATTGGCCCGTTCCCGACCGACGCCGAGGTCGACGCCGACCTGATCAACGCCGGCAAGCAGACCGTCACCGCACGCGCCGGCGCCAGCTACTTTGGCAGCCACGACAGCTTCGCGATGATCCGCGGTGGTCACGTCAACCTGGCCATCCTCGGCGCCATGCAGGTCACCGACAAGGGCGACCTGGCCAACTGGATGGTGCCCGGCAAGATGGTCAAGGGCATGGGCGGCGCGATGGACCTGGTGGCTGGCGTGCAGCGTGTGGTGGTGCTGATGGAGCACACCGCCAAGAACGGCGAGCACAAGATCCTGCCCGAATGCACGCTGCCGTTGACCGGCGTGGGCGTGGTCGACCGCATCATCACCGATCTGGCGGTGTTCGACGTGACTGACAAGGGCTTGCTGCTGGTGGAGGCCGCGCCGGGTGTCAGCGATGAAGAGCTGAAGGAAAAGACCGGCGTCGCGTTCCAGCGCGGCTGACGGCACGAGGGCGGCCCAAGGCCGCCTCGTTTCCTGAGGGATTGCCATGCTGTTCCCCCACGACCTGCCCGATGCCGATGTCCTGCACCTGCCGGGCTGGCTGGCTGCGGCCGACGCCGACCAGCTCCTGTCCTCGCTGCAGGCCGAAGTGCCCTGGGAATCCCACCGCATCCGCATGTTCGGCAGCTGGGTGGACTCGCCGCGGCTGAGCTGCTGGATCGGCGACCCGCAGGCCCGCTATCGCTATTCCGGTGCCGAGTTCGTGCCGCACCCCTGGCCGCCTGTGTTGCTGGCCGTGCGCGAGCACCTGCGGGCCGAAGGACACGGCCACTTCAACAGCGTGCTGCTGAACCGCTACCGCGGTGGCGGTGACTACATGGGCTGGCACAGCGATGACGAGCCGGAGCTGGGGCCGGCCCCGGTGATCGCTTCGCTGAGCCTGGGCGCGGCGCGCCGATTCCTGCTGCGACGCCGCGACGACCCGGCGCGCAAGGCTGAATTCGTGCTGGGCCATGGCGACCTGCTGCTGATGGCCGGGCAGACCCAGCGCTTCTACCAGCACGCGCTGCCGAAGATGGCGCGGGTGCAGGGCGAACGGATCAACCTGACCTTCCGCTGGATCACGCCACGGTGA

Protein sequences of DBSCAN-SWA_2

>NZ_CP021768|620854:629235|627232_627967_+|WP_087921460.1|DBSCAN-SWA
MSNPATTGGKRGKRFASAAEALQGVVADGQTLAVGGFGLCGIPEALIAALRDSGVKGLTVISNNAGVDGFGLGQLLETRQIKKMISSYVGENKEFERQFLAGELELEFNPQGTLAERLRAGGAGIPAFFTATGYGTVVAEGKETREFDGKHYVMETALRADVALVKAWTADEAGNLVFRKTARNFNPACAMAGKVCIVEVEEVVPVGAIDPDQVHLPGIYVHRIVHNAHPEKRIEQRTIRAEGN
>NZ_CP021768|620854:629235|621924_622812_+|WP_087921455.1|DBSCAN-SWA
MTQRKGIILAGGSGTRLYPITKGVSKQLLPVYDKPMIYYPLSVLMLAGIREVLIINTPHEQALFQQLLGDGSQWGMDIQYAVQPSPDGLAQAYLIGRDFVAGKPSCLVLGDNIFHGHGLREVLKRADERVHGSTVFGYWVNDPERYGVAEFDQSGKVIDLVEKPEKPRSNYAVTGLYFYDGNASDYAAELKPSPRGELEITDLNKRYLAEGNLHLEALGRGYAWLDTGTHQSLLEASNFIETIQTRQGLQVCCPEEIAFGKGWISAEQLEALAAPLIKNGYGQYLHTLAQRGVVP
>NZ_CP021768|620854:629235|624331_625735_-|WP_087921458.1|DBSCAN-SWA
MSSIQPVILSGGSGTRLWPLSREAYPKQFLPLAGELTMLQATWKRVAPIAARGPLVIANEEHRFVAAEQLQQVGAEPAAIILEPVGRNTAPAIAVAALEATRDGADALLLVLPSDHVITDEAAFRAAVQAAAGAAEAGKLVTFGIVPTGPETGYGYIKAADGQGLRAVERFVEKPDLDTATDYVSSGQYYWNSGMFLFKASRYLQELERFQPAMLVGSRQAWQQARRDADFTRLDKDAFTAVPSDSIDYAVMEKTADAVVIPLDAGWNDVGSWTALRDVSQQDGDGNAHQGDVIAIDCRNTYAYAQRLVALVGLDDVIVVETDDAVLVGKADRMQEVKTVVAQLKAEGRSEATWHRKVYRPWGAYDSIDNGERFQVKRITVKPGGTLSLQMHHHRAEHWIVVSGTAEVTRGDEVILLSENQSTYIPLGVTHRLRNPGKLPLELIEVQSGSYLGEDDIVRFEDTYGRS
>NZ_CP021768|620854:629235|620854_621910_+|WP_087921454.1|DBSCAN-SWA
MPTWLVTGGAGFIGGNFVLEAVARGVKVVNLDALTYAGNLKTLSSLDGNPNHVFVQGDIGDSALVTRLLAKHQPDAVLNFAAESHVDRSIDGPGAFIQTNVVGTLGLLEAVRDYWKALPAEQGAAFRFLHVSTDEVYGTLGETGKFSETTQYAPNSPYSASKAASDHLVRAFHHTYGLPVLTTNCSNNYGPYHFPEKLIPLVIAKALAGEPLPVYGDGKQVRDWLFVSDHCEAIRTVLAKGQVGETYNVGGNSEKQNIEVVQAICALLDQRRPRADGQPRSSQITYVTDRPGHDRRYAIDASKLKNDLGWEPAYTFEQGIAYTVDWYLDNQDWVNGVLDGSYRLQRIGTTA
>NZ_CP021768|620854:629235|623362_624256_+|WP_087921457.1|DBSCAN-SWA
MTVLVFGGNGQVGQELLRALAPLGAVVATTRSGTLPDGSACETADFSQPDSLPALLDRLQPSVVVNAAAYTAVDRAEQDVEAAFAANAQAPGVIARWCAAHGVPFVHYSTDYVFDGQGSAPYREDEPTAPLGVYGTSKRDGEDAVRAAGGRHLIFRTAWVYASHGANFLRTMLRVGAEREQLRVVADQIGTPTPAALIADVTAQALQHPGQLSGTWHLTASGQTSWHGFAEAIFAEALATGALAKVPTVEAIPSSEYPTPAKRPAWSVLDNRKLQQDFSIVLPAWQDGLKRVMAEIA
>NZ_CP021768|620854:629235|625746_627093_-|WP_087921459.1|DBSCAN-SWA
MPLPAFKAYDIRGRVPEELNEELARRIGVALAAQLAPGPVVLGHDVRLTSPALQDALAAGLRGTGREVIDIGLCGTEEVYFQTDHLGAAGGVMVTASHNPMDYNGMKLVKENARPISSDTGLFAISDAVAADTSEAQPPRAGQSAQHDKSAYIQHLLSYVDAPKLRPLKLVVNAGNGGAGAIVDLLAPHLPFEFIRICHEPDGSFPNGIPNPLLPENRAATADAVREHGADFGIAWDGDFDRCFFFDHTGRFIEGYYLVGLLAKAILARNPGGKVVHDPRLVWNTVDMVEQAGGVPVQCKSGHAFIKEKMRAEDAVYGGEMSAHHYFREFAYADSGMIPWLLIAQLVSESGRSLADWVEDRMAAYPCSGEINFKVADAKAAVARVMEHFAAQSPALDHTDGISADFGDWRFNLRSSNTEPLLRLNVEARGDAALMQARTDDISRLIQQ
>NZ_CP021768|620854:629235|627968_628601_+|WP_087921461.1|DBSCAN-SWA
MAWTRDEMAARAAQELTDGAYVNLGIGLPTLVANHIPDGVDVWLQSENGLLGIGPFPTDAEVDADLINAGKQTVTARAGASYFGSHDSFAMIRGGHVNLAILGAMQVTDKGDLANWMVPGKMVKGMGGAMDLVAGVQRVVVLMEHTAKNGEHKILPECTLPLTGVGVVDRIITDLAVFDVTDKGLLLVEAAPGVSDEELKEKTGVAFQRG
>NZ_CP021768|620854:629235|628647_629235_+|WP_087921462.1|DBSCAN-SWA
MLFPHDLPDADVLHLPGWLAAADADQLLSSLQAEVPWESHRIRMFGSWVDSPRLSCWIGDPQARYRYSGAEFVPHPWPPVLLAVREHLRAEGHGHFNSVLLNRYRGGGDYMGWHSDDEPELGPAPVIASLSLGAARRFLLRRRDDPARKAEFVLGHGDLLLMAGQTQRFYQHALPKMARVQGERINLTFRWITPR
>NZ_CP021768|620854:629235|622808_623366_+|WP_087921456.1|DBSCAN-SWA
MKVIETSLPGCRVIEPAVFGDERGFFFETWNAERFTALGLPDRFVQSNVSSSAKGVLRGLHFQWPRPQGKLVSVLEGEVYDVAVDIRRGSPTFGRWEAVVLSAENRKQFWIPEGFAHGFAVLSERALFSYLCTDVYVKETDAGIRWNDADIAIDWPISAPTLSAKDENAPFLKDIAEDRLPVYTP

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087921454.1|620854_621910_+	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	7.3e-84	47.7
WP_087921455.1|621924_622812_+	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	5.3e-96	58.1
WP_087921456.1|622808_623366_+	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	2.4e-46	51.7
WP_087921457.1|623362_624256_+	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	2.1e-28	38.6
WP_087921458.1|624331_625735_-	mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase	A0A1V0SH58	Hokovirus	1.2e-46	29.1
WP_087921459.1|625746_627093_-	phosphomannomutase	A0A127AWJ1	Bacillus_phage	6.5e-29	26.1
WP_087921460.1|627232_627967_+	CoA transferase subunit A	NA	NA	NA	NA
WP_087921461.1|627968_628601_+	CoA transferase subunit B	NA	NA	NA	NA
WP_087921462.1|628647_629235_+	alpha-ketoglutarate-dependent dioxygenase AlkB	A0A2K9L0M4	Tupanvirus	9.5e-25	34.3

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP021768|1641260:1652169|DBSCAN-SWA
GATGGACGTTCGTGAGAAGCTGGCAAGGTTGAACCCGACCACCGTCAAGTTCGATACGGGCCACGGTGGCGTTGCGGAGCTTACCAATCAGGACATTGCGGCGGCGCTGGCGTTTGTGCCGCAGGGATTGGGACGAGAGGTTCTTGAGGCTTGCTGGTGGCCCTGGGGCGCGGCGATCCGTGCCAACGGGCTGCGCAACTCTGTCATGGCAGTAGTAGGCCCGGAGCTTACTCGTCAGTCGCGCCGGGTGTCGCAGGCGAGCCTTGACCTCCAGCTGGCCGAGGCAGCCATTCTTTGGGGTGGTAACTCAGTGAGCGCAGAGGCGCGGGCAGAAGTTGACCGCTGCCGTTCCAGGCTGGCCGTCGTGCGTGGCGAGTGCTGGCCGAACAATACAGCTGAGCGCTTGCCGCTGATTGCCAAGGCCATCGTTAGTGAAATCCATGGGCACCGCTGCACCAACTGCAATGGAACCGGCAAGGATCGTGGAGAGAACTCGGTATGCAGGTCCTGTGAGGGCAGCGGCAATGCCAAGATCCTTGACGCATGGCGTGCCGCCGCGATCAAGGTGGATCCGTCCGACTTCCCTAAGCGCTGGAAGCGGGTCTATGAGTGGCTTTTCGTAAAGATGCGAGATGCCGAGGCCGAGGCCGGCAGAGCCCTTGAGGCGGCACTGAGGAGGGAGGCTGCCTAATGTTCATTTTCAGTGAGAGCCGCCTTGAACGGGTGGAGGCCGCAAGGATCATGCGGGAGCTTGATCCAAAAGAGTGCTGCCTCTATGTGATGTTTGCCAAGGATGGCGAAGGACCCATGTACATAAAGGTTGGAATCAGTGAGTGCCCAGGTAAGCGGGCGAGGCATGTCCAAACCGGTTGCCCCATCCCAATTCGCAGGGTGATTGCGTTCCGTTGCAGTAGTCGCCGGACCGCCAGGAGTGCCGAGATGGCAATGCATGAGGCAATGAAGGAGCACTCAGCCACCGGGGAATGGTTCCGGTTGGAGTGGGGGCAAGAGGCAAAGGACTCTCTGCACGCGTTGATCGAAAAGGTCATGGATGCAATTGGCGGAGTCGACCTAAAGGATGTGACCGACGAAGACACCCGTGTTGCTGTCAGGAAGAAGCAAGAGACCTGGGAGTCTGCGCAGAAGAAGGCAAAGGTGGCTGCCTACAACAAGTACCGTCTAACAGTGGAGTTGCGCGCTCCACTTCGAGTCGCATAATTTCATATCATCGCGCACGACCCACGCCCCGGCACCCGCTGGGGCGTTTTTGTTGGAGCAGACCGTGGCCTATCCCGACAACAACCCCAAGACGGCGGTTGGGGCGGCCAAGGTTCCGCTGCACCTCGTCCCGCCCAGCGCCAAGCACTATCTGGCCCTTGCGCTAGCTGATGGTGCCAAGAAGTACGGCCCCTACAACTGGCGGGATTCGGCTATCAGCGTTTCGGTCTACGTGGCAGCAGCCCAGCGGCACCTAGACGCGTTCTGGGATGGAGAGGACTGCGCCGACGACTCGGGTGTGCACCACCTGGCGCATGCCATGGCCTGCTTTGCGCTCCTGCTGGACGCCAAGGAGGTCGGGATGCTTCACGACGACAGGCCCAAACCTGGGGCAACCCATAAGTTGCAGATGAAATATGCAACTCTTAATTTGCCACGAACCGACACGGGTGACTAATGAAATGCCCTCGTTGCGGAGCAGATGGAGCTACGAAGAACGGCACAGGCCGGTGCTTCTGTAAGACCTGCGGGAAGTTCGGTGTTATTCGCCCGCAGGATCGGGAAGACCAGCTGCTTGCCGCCAAGGGTGGTTGGGCACCTGACTGCCAGCTAGTGCACCCAGCGGCGCCGGGGTTTGAGGTTCGTGGAACCTCGACCCTGTACCGAGACGATGGCACGGTTGCCGCCCAATGGGTCAAGACGCGGCAGGATGACGCTGCAATGGCTGCGGCGATGGAGTCAGCCATTGTTGCGCTGGCGGAGAAGATCCCGCGAGAGAAGGCGCGGCCAGCCCCGAAGCGGACGTTGGATGACCTGGCGAACGTCTACGTCCTGACCGACTACCACCTGGGCATGCTGGCCTGGGGCGAGGAGACCGGCGCAGATTGGGATATCAAGATTGCCGAGGATATGCTGGTTGACTGGTTCGCGGCGGCTATTGCTGCTGGACCGGCCGCCAAGGTCGGCGTTCTGGCTCAGCTTGGCGACCTGTTGCATTGGGACGGGCTGGAATCGGTGACCCCGACTTCCGGACATGTTCTGGACGCTGATAGCCGGTTCCAGAAGCTGATCCGCGTGGCGATTCGTGTCATCCGTCGCGTGATCGGAATGCTGCTGGATCGGCACGAAGTGGTTCACGTCGTGATGGCTGAGGGCAACCACGACCTGGCTGGTTCGGCGTGGATGCGCGAGTGGCTGTCGGCCATGTACGAGAACGAGCCGCGTGTATCGGTGGATACCTCGCCAGACCCGTACTACTGCTACGAGCATGGGCAGACTGCTCTGTTCTTCCACCACGGTCACAAGAAGCTCATGGCGCAGATCGACACCGTGTTTGCCGCGAAGTTCCGCGAGGTGTTTGGTCGAACGAAGCACGCCTACGCCCACATGGGGCACCTTCACCATATCGACGTGAAGGAAACGAACCTGATGGTGATCGAGCAGCACCGGACCCTTGCGGCACCGGATGCTCACGCCAGCCGGGGCGGATGGATGAGCGGGCGGGATGCCTGCGTTATCACGTACTCGAAGAAGCATGGCGAAGTTGGCCGGGTCCGGATCAACTCGCAGATGCTGGAGGCAGCATGACCACTATCGCCGTAAAGGATGGGGTCATGGCTGCGGATACGCAGCTTACGGGCGATTCCATCCATAGAGTGCCAAAAATCTTTGAACTGCCTGACGGCGGCCTCATCGGTGGATGTGGTGAGTCGTGGTCCCGAACCTATGCAGTAATCAATTGGTTCTTATCGGGACAAGAGGGTGATGCGCCAGAGTTTGAGGATGGTTGCATACTGATATTGCAGCCTGACGGACAGATCCTAATGGCTTATGACCGCCTTCCCGCATTTCCCATCATAGGCGCGACGGCAGCGATTGGCAGTGGCGGCCCTATCGCGATGAACCATATGAGCAGTGGCGCTAGTGCCGAGAAGGCGGTTAGGGCTGCATGCATGACTGAGCCGTACTCAAGCGAGCCGGTGCAAGTGTTCAAGCTGCCAAAGCGGCGGAAGAAGAATTCCTCTTAGCTCCGGCAGGGAGCGGAGGCTATTCCGGGGTAGCTACCCGGACGTAAGGGGGCGCTCTGGACTGTCATCCATCGCCACTGGATCCCAACCAGGCCGCCACGCAGTTGCGGCACCACTTTCCATGCCCAGCCCCGGACCATTGAGCCGTGGATGCCTGCCTTGCGCAGCGCTGGGCACCTATTTGAGGAGTCCGCATGGCGGATCTTGACCACATTCTTTCTCGCGTGGTCGGTCCCGGCCTTGCACTGCTTCCGTCAACGATGGATACCGCCAAGGCACGGGTGTTGCTTCTGGCGATTGGCCTGCAGGAATCTCGATTCGAGACGCGGCGCCAGATCGGTGGCCCGGCTCGGGGCTACTGGCAGTTCGAGAAGGGCGGTGGCGTGGTCGGCGTCCTGACTCACCCGTCCACCCGCAAGTATGCGGCTGATGTTTGCAGGGATCGAGGCATTGAGCCGACAGCTGCGGCGGTCTATCCGGCGTTGGAGCGAGATGACCTATTGGCCTGCGCCTTCGCACGGCTGCTGCTGTTTACCGATCCGAAGCCAATCCCTGATATCGGCTACCCAGCCGCATCGTGGGACTACTACGTCCGCAACTGGCGTCCTGGCAAGCCCCATCAAGGCACTTGGGACGCCCTCTACGCAAAGGCCGTGGAGGCGGTGCGCTGATGGATGACGTGACTGTTTGGGGTGTAGGTAGCGGCGTCGGCGTGCTGCTGTTGCTGGGCAAGCTGGCATGGGACCGTTTCCTTTCCCCCGAGGCGAAAGCCAATGACGCGCTGGTGCAGCAGCTGTCTGAGCGCATCACCGCCCAAGAGAACCGGCTTGTCCTGCTGGAATCTGGCTTGGACGAGGAACGGAAGGCTCGCCGTGCCGCAGAGACGAAGGTCTATGACCTGACGATGCGGATTATGCGGCTGGAGTTCGAGTTGAAGAAGCACAACATTGAGGTGCCGCAGTGAAGATCGAACAAAGAACGGTCATTCAAGACCTGTGGGTGGCCGTGTACCTGCATTATGTTCATGTAGGTTCACCCCATGAGGTGGCATCCAGAAATGCGGACGATGCGGTCGCGGCGTTCATTGCCACCTTCTCTAAGATCTAGGTATTGCCATGCGCATCCTAGCCGTCCTACTGCTGGCCTCACTGGCTGGTTGCGCTGGAGCGCGCCCGTCAGTTGAGCGGTACACCTACCGAATTGGCATGCAGGACGGCGGCCTATGTAGTGCTACGGCAGTGGGGCGTGAGGTCCTACTGACAGCAAAGCACTGCATCACTGAGAAAGACTCGGTCGTCTACTTCGGCGACAAGCGCGTGACCATCCGCCATATCGAGGTGGACGGCCATGACCATGCGCTGCTGTGGGTCGATCAGCGGTTTCCGGTATGGGCGCAGCGCGGTCCGACCACGCACAAGGGCGACGGGCTGTCGTTCGTCGGCAATGTTGATGGATTCGATCAGTTCTACCGGTCGGGCCAGATGGCGGGTTGGTACAGCTCGGCGATGCTGCTGGACATGACCTGCGGCAAGGGCGACTCGGACGCCGGAGTATTCAACGAGTCCGGCCAGCTGGTCGGCATGGTCAGTGCGGTGTACGTGGGGCCGATCGTTCGGTTCTGCGTGTCCTACCCGCTGGCGTTCAGCCCCAAGCAGTGGGCGCGAATCTGACAGGAGTTTGATATGGGCACCAACTTTTCTGATAGTTGTTCGCAGTCTGAGCCTGAATTTGAACGTAACAGTCTCCGAGACAGACTTCAGATTACTGATTCGCAAATCGAGCAGCTCATCCATCAAATCGAGCGACTTGAGGCACGACTAGAGCCGGTCCTTACTCCATGGCTTTGTGGTGAGGCGTACAAGTCCGATCCTGAGCCATCACGCAGCCCCGTGGCACAGATTGCTCACGATCAGGGCGTCCGCGTCTATCAGGCACATTTGCGGCTTGCGGAGCTACTCAACCGAGTGGCGATCTAATGTCATGGCTCCTGAACCGGCAACTGTGGCTATTTGTCGTCCTTGCGACCATTGCCGGGCTCTTGTTCTGGCGCGGTGGATCGCATGCCAGGGAGGAGGCGAGGGAACTGCGTCAGGAGGCCAAGCAGACGGCCAGGTCCAACGAGATCAGCCGTGGCACGCAGCAACGGATCGGGATTGAGGGCTATGAAGTCCAGAAGCGAGCCAAGGCCGATGATCGGGCGCTGCGCCAAGGTGCTTACCCTGCTGCTACTCCTGCCGATGATGGCGGGATGCGGGTTGCTGAGCAGGCACACAAAGCAGCCCTACGTGCCGCCTGCAGGGTGCGGGGAGAGAAGTCCTGCGATGGAACCACCGGCCCCTGAGAACACCACGGATTGGCGCATCTGGCGCGCCCTGTATGTGGGGTCGGTATGGGCATATGTGGACTCGGAGAACAAGCGAGCGGCTACCGCCGACTGCCTGGACAAGCACAGGGGAGCAAAATGAGCCTGATAGAAATGTTTGCTGCGCTGTGCGTAGGCCATGCGCTAGCCGATTACCCGTTACAGGGCGACTTTCTCGCCCGTGCTAAGAATCGATCCAATCCTTTGACGGGTACGCCATGGTTTCAGGCGCTCGGCGCTCATTCGCTGATTCATGCTGGATTTGTTGGTCTGATTACCGGGAGTCTATGGCTTGCGGCGGCGGAGTTCTTGGCGCACGCGGCAATCGATGACCTGAAGTGCACAGGAAAGATCGACTTCAACGCCGATCAAGTGCTGCACATCATCTGCAAGTTGGTCTGGACAGTCATTGCGCTCGCGGGCGTGCCATGAACGAGATGGACGCCAAGGGCGCCGAGTTCGTGGACGCCTGCCAAGACGCTGGAACGTATGGCGTGGCCCTGCGACTGCTGGACAGCGCAAACATCCGAATCATCAGCCTCAAGGTTCCGATGAAGGCATTGGCCGCATTGCTGAGGCAGGCGGCAGACATTTGCGAACAACAGGCCGACACAGACCGGCTGAACTGAGGGATTGAGATGGCTGATAAGCCGGGCGCGTTTCGAAACTTCTTTGGCAGGTTTGTCCAGGCTGCCTTGCCGGGAGATAACTACAACCGTCAGACCGGCCAGTTCAGCAACATCGGCACTGGCTTGGCGGGACTTGGTGCACGGCTGATTGCCACTTCACTTGCAGGCCCTGCCGCTGGTGCACTGGTTGGCCGCGCAGCCAACTATCTGATCGACCGCAACGGCAATCAGATCGGCCCTGTGCAGCGCGAAGGTGTTCCGGTAACGGGCGCCCCCGCATCAGTCCAGAACGCAATTACCGCACCCAGTCCGCTGGCAGTTAACAACCTGGGCCTAGGTGCCCAGCGTCCGGGCGGCAACTGGTACGGCTACACGGGCGGAGCTGGCTCTATGGGGAGCTTCGGCAACACCCAGTTCGGCAATGGGATGGCAAGCATCGGCCAGTGGAACCCACAGAGCGTATGGGGCCAGCAGGTAGCGGCTCCGACTGGGTCGAACCTTGGGCTGGGCAACAACGTGGGCGGCTTCATTGGGGGTGGCTCAGGCGGCGGTAGCGGCCAAGCAACTGGAGGCGGCATGCCAGGCATCGTGGGTGGCCGATTCGCAGGCAGTAACCCCGTGGACTACAAGCGCGGTTTCATCACAACGAAGAAAGCATAGGAGAGCAAATGCCGACTTGGCTGAGCAACAAAGAGATCGTGATCATCAAGACCTTCAACGGCTGGGCCGTGGGTTCGGACAAGGGTGCAGACGCTCGGGACTGTGTGGCCTTCGAGACATGGGATGCGCTGGTGTATTGGCTGAACGCCCATTGGGTTGCACCGGCCCCGTAACTGAATGAATTAAATCAAGGATTCATCTATGGCACGCGGAGGCAAGCGCCCCGGCGCCGGCCGACCACCGTTGGCCAAGAACAAGATCCCCATGGCGGCCAAGGCAATGATCGAACAGGTCGCCATGGGGCTGGGCGGTGCAGAACGGATGTTGACCTGGGTTCAAGAGGACCCGGCCAACGAGAAGGCGTTCTGGACCGCGATCTATCCGAAACTGCTTCCCTTGCAAGTGCAGGGGGACAAAGAGAGCCCGTTGAGGGTTGTGACTAGCATCAGGCTGGAGGCGATGCATGACGACAGCATCCGTCCTGCTGCCGAGGAAGCTGATCCCAGTATTTGACGGCCCGGCCGACGTTCGAGGCGCATACGGTGGTCGAGGCTCGGCCAAGACCCGTAGCTTTGCAAAGATGCTCGCTGTCCGTGGATACATCTACGGGATGGCGGGCATTCGCGGCCAGTTGGTTTGTGGCCGCCAGTTCATGAACTCCCTGGAGGACTCATCTCTAGAGGAGGTTAAGCGGGCCATCGAGGATGAGCCATGGTTGCTTGACTACTACGAGATCGGCGAGAAGTACATCAAGTCAAGAGACGGGAACATTTGGTTCACGTTCGTCGGCTTGGATCGCAATCTTGGCTCGATCAAGTCCAAGGGCCGAATCCTGATCTTCTGGATCGATGAGGCTGAGCCTGTAACTGAAGAAGCATTTACCGTTGTCGGCCCGACCCTGCGCGAAGAGGGCACCGGCTGGAACGCAGAGCTTTGGCTGACCTGGAATCCAAAGAGGGAAAAAGCGCCGGTTGAGCGCTACAGACACTCGAAAGACCCACTCATCAAGGTTGTAGAGCTCAACCACACCGATAACCCGAAGTTCCCTGCGAAGCTTGAGCGAGAGCGACGCAGAGACCTTGATGAGCGACCGGAGCTATACGGGCACATTTGGGGCGGCGAGTATCTGCGCGCCGTGGATGGGGCGATCTACCTGCAGGAAATGACCGCAGCCGAGCAAGAGGGACGCATCAGTGCTGTCCCATACGACCCTCGGCTCAAGGTGCATCTTGTCTTCGACCTTGGCCACAACGACGCCATGTGCGTGGTGCTAGTGCAGCGTCAGCATGGTCAGCTTAGGGTTATTCGTGGGCTTACTTGGCGTGGCAAGACGCTTGAGTACGTAAACGCCGAGCTACAACCCCTAAAGCTCAACTGGGGAAAGATGTTCCTGCCCCATGACGGCGAGAACGGGTCCTACCTGGTTGGTCAGAACGCCCGCCAGATCATGCAGGGCTACGGGTGGAACGTGTCGATCATTCCTAAGTACACGGGATGCGTGGAGATCGGCATCCGTAAGGCCAAGTCAATGTTCCCGAGAGTCGTTTTCGATAAGGACGGCTGCGCTGACGTAAAGACGGAGACGGGCAGCGAGCTTCCTGGCCTCCTCACTGCACTGGGCCAGTACAAGCGGCACATTCCGACGACAACTGGCGAGCCCGGAGCCCCAGTCCACGACAAGCACTCTCATTTCGCTGACACGTTCCGCTACGTGGCCGAAGCCGAGCCGCAAATGACTAACGACACCTGGGGAGAAGCCCCCGTGCATCGACCCAACATGAGGTACGTTTGATGGCAGACGACTACGAGTCGCTAGATGTCGCCGAGGTGGATAGCCCGGAGATGACAAACGATGAGCTTGCCGCGCTGATTGACCATGAGAATGCAGTCGCGATTGGCGTGAACGATCAGTTCGCGTCTGACCGCGAGGAGATGCGCTACTTCTACATGGGCGAGGCGCGGGGCAAGCTCCTGCCGCCAGAGGGCGACGGCCATTCGCAGGTGGTCGATAAGACCATGATGGACACGGTCGAGTGGCTGCTGCCGTCGCTGATGAAGATGTTCAGCCAAGACGGTGTTGTTATCTTCGAGCCTGACTCGCGTCAGGACGAGAAGGCAACCAGGGAAGCGTCGAACTACTGTAATTACCTCTTCTTCAAGGAGAACGAGGACGGCTTTACCACGCTGCACGACGCGATCAAGTCGTGCCTGATGTTCCGCATGGGCGTCACCAAGACGTGGTGCGAGAAGGCTTGGGAAGAGCGGCGGGAGGTCTATCGCGGCCTCTCACTGGCCGAGGTTGAGGCCATGTCCCAGGAGGAGAACGTCGAGATTGCCTCCATTGATGAGGCAGGGCAGCTAGACCCTACGCTGGTTCCAGAGGGTGCGCCTCCGGAAGCTGCGCTGCTCTATGACGTGGTTCTGAGCATCAAGGAACAGAAGAACCGGATTAAGGTGGCAGGTGTGCCCCCGGAAGAGATCCGGATTGCCCGCGACACGCGCACCATGAGCGACGTTCGCTACATCGCCCACGTGGTCGAGCGGACTCGGTCAGACCTCCTGTCCGAGGGCTGGCCCGAAAGCGAGGTGGACACTTACTGCGGGTCCAATGAGGCCGATGAGGGGCAGTGGGAGAAGGACGAGCGGCACGAGTACGACGGGTCTGAGGACTATGGAGACGCCCAGGGCGACGAGAGCCAGAAGAAGGGCATCGTCACTGAGTGCTACATCAAGGTGGACTTCGACGGCGATGGCATTGCCGAGTATCGTCGGATTGTGAAGCTGGGCCGGTACATCCACATCAACGAGATCACGGACGACCATCCGTTCTCGCTGGCGACGCCGATCTTGATGCCGCACAAGCTGATTGGCTTGGGCATGTGGGATCTGGTTGAGGATCTGCAGCGCATCCGCACCGCGCTAACCCGACAGATGCTGGACAACGCTTACCTGGTTAACAACCCGCAGACGACGATTGTCACCAACCAGGTCAATCTGGACGACCTGGCAAATCCGCGCCCGGGTGGCTGGCGCCGTGTGGAGAGTCTTGACGCCTTGCGCGTTGACGTGACGCCGTTCGTTGGCCCGCACGTGCTGACTCTGCTGGATCACTTCGGGCAGGTGCAGAACACTCGCACTGGCGTTACCGAGATGAACTCGGCTCTGAATGCGGACTCGCTCGCAAAGGGCAACATCGGCTCGGAGGGCATCTCTGAGCTGATCGGGCAGGGCGCCCAGCGCATTGAGCTGATTGCCCGAGTCATCGCCGAGACGTTCATGAAGCGTCAGTGGCGGCTTCTGCTGAAGATGGCAAAGCAGTACACCGACCGAGAGAAAGAGATCAAGGTCAACGGTGACTGGCTGGTCATCGATCCGCGCCAGTGGAAGAACCAGTATCGGATGACGGTATCGGTTGGTGTTGGCAATCAGGGCGAGGCGAAGAAGATGCTGGGCCTGCAGACGATTGCGGGCGTGCAGCAGCGTGCGTTTGAGCTGGGGATTGTCACTCCTGAGAACGCCATGAATCTTGCGCTGGATATTGCCCGTGCGTCAGGTGAGAAGCAGCCTGAACGGTACTTCAGTCCGCCTCCGCCGCCAAACCCAAACCCGGGACCGCCGCCCGAGGTTCAAGTGGAAATGGCAAAGGCCCAGACGCAGATGCAGCTGGCTCAGATGAAGGGACAAGTTGAGATTCAAGTGGAGCAGCTGCGGCAGGAAGCCCAGGCGCAGCAGAATGCACTGGAGACGCGCCTTGAGGCTGAGCGTAATGAGCTTGATCGGCAGAACCAGGCGCAGATTCAGCGGCTGAAGATCCAGCAGGAGGCCGAGTTGGCTGCTCTGAAGCTTCAGTACGAGGATGCCGACCGCCAGCGGGAGCGAGATTTCCAGCGGTGGAAGGCCGAGCTAGACGCGTCTGTAAAGATCGAGACGGCCAATATCAGCTCGAAGGCCAAGGTAAATAACCCGGCTACGCAAACGGCAACCGACGAGATCGCACGGGAGGTGCAGCCGTGA

Protein sequences of DBSCAN-SWA_3

>NZ_CP021768|1641260:1652169|1641260_1641950_+|WP_087922143.1|DBSCAN-SWA
MDVREKLARLNPTTVKFDTGHGGVAELTNQDIAAALAFVPQGLGREVLEACWWPWGAAIRANGLRNSVMAVVGPELTRQSRRVSQASLDLQLAEAAILWGGNSVSAEARAEVDRCRSRLAVVRGECWPNNTAERLPLIAKAIVSEIHGHRCTNCNGTGKDRGENSVCRSCEGSGNAKILDAWRAAAIKVDPSDFPKRWKRVYEWLFVKMRDAEAEAGRALEAALRREAA
>NZ_CP021768|1641260:1652169|1645174_1645468_+|WP_087922149.1|DBSCAN-SWA
MDDVTVWGVGSGVGVLLLLGKLAWDRFLSPEAKANDALVQQLSERITAQENRLVLLESGLDEERKARRAAETKVYDLTMRIMRLEFELKKHNIEVPQ
>NZ_CP021768|1641260:1652169|1646479_1646845_+|WP_087922151.1|DBSCAN-SWA
MSWLLNRQLWLFVVLATIAGLLFWRGGSHAREEARELRQEAKQTARSNEISRGTQQRIGIEGYEVQKRAKADDRALRQGAYPAATPADDGGMRVAEQAHKAALRAACRVRGEKSCDGTTGP
>NZ_CP021768|1641260:1652169|1646965_1647298_+|WP_087922152.1|DBSCAN-SWA
MSLIEMFAALCVGHALADYPLQGDFLARAKNRSNPLTGTPWFQALGAHSLIHAGFVGLITGSLWLAAAEFLAHAAIDDLKCTGKIDFNADQVLHIICKLVWTVIALAGVP
>NZ_CP021768|1641260:1652169|1647294_1647495_+|WP_157721511.1|DBSCAN-SWA
MNEMDAKGAEFVDACQDAGTYGVALRLLDSANIRIISLKVPMKALAALLRQAADICEQQADTDRLN
>NZ_CP021768|1641260:1652169|1643197_1644064_+|WP_087922146.1|DBSCAN-SWA
MAAAMESAIVALAEKIPREKARPAPKRTLDDLANVYVLTDYHLGMLAWGEETGADWDIKIAEDMLVDWFAAAIAAGPAAKVGVLAQLGDLLHWDGLESVTPTSGHVLDADSRFQKLIRVAIRVIRRVIGMLLDRHEVVHVVMAEGNHDLAGSAWMREWLSAMYENEPRVSVDTSPDPYYCYEHGQTALFFHHGHKKLMAQIDTVFAAKFREVFGRTKHAYAHMGHLHHIDVKETNLMVIEQHRTLAAPDAHASRGGWMSGRDACVITYSKKHGEVGRVRINSQMLEAA
>NZ_CP021768|1641260:1652169|1642541_1642934_+|WP_157721509.1|DBSCAN-SWA
MAYPDNNPKTAVGAAKVPLHLVPPSAKHYLALALADGAKKYGPYNWRDSAISVSVYVAAAQRHLDAFWDGEDCADDSGVHHLAHAMACFALLLDAKEVGMLHDDRPKPGATHKLQMKYATLNLPRTDTGD
>NZ_CP021768|1641260:1652169|1647504_1648155_+|WP_157721512.1|DBSCAN-SWA
MADKPGAFRNFFGRFVQAALPGDNYNRQTGQFSNIGTGLAGLGARLIATSLAGPAAGALVGRAANYLIDRNGNQIGPVQREGVPVTGAPASVQNAITAPSPLAVNNLGLGAQRPGGNWYGYTGGAGSMGSFGNTQFGNGMASIGQWNPQSVWGQQVAAPTGSNLGLGNNVGGFIGGGSGGGSGQATGGGMPGIVGGRFAGSNPVDYKRGFITTKKA
>NZ_CP021768|1641260:1652169|1641949_1642477_+|WP_087922144.1|DBSCAN-SWA
MFIFSESRLERVEAARIMRELDPKECCLYVMFAKDGEGPMYIKVGISECPGKRARHVQTGCPIPIRRVIAFRCSSRRTARSAEMAMHEAMKEHSATGEWFRLEWGQEAKDSLHALIEKVMDAIGGVDLKDVTDEDTRVAVRKKQETWESAQKKAKVAAYNKYRLTVELRAPLRVA
>NZ_CP021768|1641260:1652169|1648618_1649947_+|WP_087922155.1|terminase|DBSCAN-SWA
MTTASVLLPRKLIPVFDGPADVRGAYGGRGSAKTRSFAKMLAVRGYIYGMAGIRGQLVCGRQFMNSLEDSSLEEVKRAIEDEPWLLDYYEIGEKYIKSRDGNIWFTFVGLDRNLGSIKSKGRILIFWIDEAEPVTEEAFTVVGPTLREEGTGWNAELWLTWNPKREKAPVERYRHSKDPLIKVVELNHTDNPKFPAKLERERRRDLDERPELYGHIWGGEYLRAVDGAIYLQEMTAAEQEGRISAVPYDPRLKVHLVFDLGHNDAMCVVLVQRQHGQLRVIRGLTWRGKTLEYVNAELQPLKLNWGKMFLPHDGENGSYLVGQNARQIMQGYGWNVSIIPKYTGCVEIGIRKAKSMFPRVVFDKDGCADVKTETGSELPGLLTALGQYKRHIPTTTGEPGAPVHDKHSHFADTFRYVAEAEPQMTNDTWGEAPVHRPNMRYV
>NZ_CP021768|1641260:1652169|1644060_1644504_+|WP_087922147.1|DBSCAN-SWA
MTTIAVKDGVMAADTQLTGDSIHRVPKIFELPDGGLIGGCGESWSRTYAVINWFLSGQEGDAPEFEDGCILILQPDGQILMAYDRLPAFPIIGATAAIGSGGPIAMNHMSSGASAEKAVRAACMTEPYSSEPVQVFKLPKRRKKNSS
>NZ_CP021768|1641260:1652169|1644698_1645175_+|WP_087922148.1|DBSCAN-SWA
MADLDHILSRVVGPGLALLPSTMDTAKARVLLLAIGLQESRFETRRQIGGPARGYWQFEKGGGVVGVLTHPSTRKYAADVCRDRGIEPTAAAVYPALERDDLLACAFARLLLFTDPKPIPDIGYPAASWDYYVRNWRPGKPHQGTWDALYAKAVEAVR
>NZ_CP021768|1641260:1652169|1648398_1648668_+|WP_157721514.1|DBSCAN-SWA
MAKNKIPMAAKAMIEQVAMGLGGAERMLTWVQEDPANEKAFWTAIYPKLLPLQVQGDKESPLRVVTSIRLEAMHDDSIRPAAEEADPSI
>NZ_CP021768|1641260:1652169|1645619_1646174_+|WP_157721510.1|DBSCAN-SWA
MRILAVLLLASLAGCAGARPSVERYTYRIGMQDGGLCSATAVGREVLLTAKHCITEKDSVVYFGDKRVTIRHIEVDGHDHALLWVDQRFPVWAQRGPTTHKGDGLSFVGNVDGFDQFYRSGQMAGWYSSAMLLDMTCGKGDSDAGVFNESGQLVGMVSAVYVGPIVRFCVSYPLAFSPKQWARI
>NZ_CP021768|1641260:1652169|1648163_1648328_+|WP_157721513.1|DBSCAN-SWA
MPTWLSNKEIVIIKTFNGWAVGSDKGADARDCVAFETWDALVYWLNAHWVAPAP
>NZ_CP021768|1641260:1652169|1649946_1652169_+|WP_087922156.1|DBSCAN-SWA
MADDYESLDVAEVDSPEMTNDELAALIDHENAVAIGVNDQFASDREEMRYFYMGEARGKLLPPEGDGHSQVVDKTMMDTVEWLLPSLMKMFSQDGVVIFEPDSRQDEKATREASNYCNYLFFKENEDGFTTLHDAIKSCLMFRMGVTKTWCEKAWEERREVYRGLSLAEVEAMSQEENVEIASIDEAGQLDPTLVPEGAPPEAALLYDVVLSIKEQKNRIKVAGVPPEEIRIARDTRTMSDVRYIAHVVERTRSDLLSEGWPESEVDTYCGSNEADEGQWEKDERHEYDGSEDYGDAQGDESQKKGIVTECYIKVDFDGDGIAEYRRIVKLGRYIHINEITDDHPFSLATPILMPHKLIGLGMWDLVEDLQRIRTALTRQMLDNAYLVNNPQTTIVTNQVNLDDLANPRPGGWRRVESLDALRVDVTPFVGPHVLTLLDHFGQVQNTRTGVTEMNSALNADSLAKGNIGSEGISELIGQGAQRIELIARVIAETFMKRQWRLLLKMAKQYTDREKEIKVNGDWLVIDPRQWKNQYRMTVSVGVGNQGEAKKMLGLQTIAGVQQRAFELGIVTPENAMNLALDIARASGEKQPERYFSPPPPPNPNPGPPPEVQVEMAKAQTQMQLAQMKGQVEIQVEQLRQEAQAQQNALETRLEAERNELDRQNQAQIQRLKIQQEAELAALKLQYEDADRQRERDFQRWKAELDASVKIETANISSKAKVNNPATQTATDEIAREVQP

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087922143.1|1641260_1641950_+	hypothetical protein	C8CLH7	Xylella_phage	4.2e-48	47.6
WP_087922144.1|1641949_1642477_+	GIY-YIG nuclease family protein	NA	NA	NA	NA
WP_157721509.1|1642541_1642934_+	hypothetical protein	M1PJC3	Synechococcus_phage	6.3e-33	56.7
WP_087922146.1|1643197_1644064_+	winged helix-turn-helix domain-containing protein	A0A088F6J4	Enterobacteria_phage	4.7e-105	64.0
WP_087922147.1|1644060_1644504_+	hypothetical protein	A0A1X9SH22	Bradyrhizobium_phage	7.9e-16	37.4
WP_087922148.1|1644698_1645175_+	hypothetical protein	A0A2H4JFP9	uncultured_Caudovirales_phage	2.0e-49	61.3
WP_087922149.1|1645174_1645468_+	hypothetical protein	NA	NA	NA	NA
WP_157721510.1|1645619_1646174_+	hypothetical protein	NA	NA	NA	NA
WP_087922151.1|1646479_1646845_+	hypothetical protein	NA	NA	NA	NA
WP_087922152.1|1646965_1647298_+	DUF3307 domain-containing protein	A0A088F6V5	Sulfitobacter_phage	1.5e-32	62.4
WP_157721511.1|1647294_1647495_+	hypothetical protein	NA	NA	NA	NA
WP_157721512.1|1647504_1648155_+	hypothetical protein	NA	NA	NA	NA
WP_157721513.1|1648163_1648328_+	hypothetical protein	NA	NA	NA	NA
WP_157721514.1|1648398_1648668_+	hypothetical protein	NA	NA	NA	NA
WP_087922155.1|1648618_1649947_+|terminase	terminase	A0A088F6U9	Sulfitobacter_phage	2.0e-75	39.1
WP_087922156.1|1649946_1652169_+	hypothetical protein	A0A218MLX1	uncultured_virus	4.8e-85	33.1

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_CP021768|3138163:3153509|DBSCAN-SWA
TTCACCACACGCCCATGCGCACACGCAGGCGCCCGGCTTCGTCATAGACCCGCCAGTTGCCATCGCTGTACTCGGTGCGGCGCCCGCCACCGGGCGCACTGACACTGAACGCATCGGCCACCACATCGAAACGCGAGACCTGACCGCTGGATGCCAGTTGCACGCCCCCTACCCGGCCATCTGCACGGACGTTGACCGACCACTGCGCGGACGACTCGGTGCCTCCAGCCGACCAGGTGGGGGGGGCGGTTGCCGACGCATCCACCTGGCTCAGCATTGGGCGGAACATCCAGAAGTACGGCGTGGTTCCACCAGTACCGATCACGATCACGCGGAAGCGAGCGAAGGATGCTGTGGCGGGCGCCTTGGTGATCAGGAACGTCCGCGTCAAGCGGTCGAGCGTGATCGGCGTTCCGGTATCGCTCCTCACGCCAGGGCTGTGCACCAGCCCCAGGTGGTTGCCGGCCGCATCGAAGAACGTCATCTCCAGCTTGACTTCCACGCGATGAGTATTGATCCAGGCGGACGCGCAATAGGTCTTGCCGCCCTCGATGGCGATGTCGTACTCGGTTCCCCACCACGCGATTTCACCTGCCGCGACGACGCCAGGTGTCACTGAGCCCAGTCCGGTGATGCCCTTCGGATGCCAGCTGTCATCGCCGGTGGGATTGCCCAGCTCGGACCAGCGGCCGTTCGGATTGCTTCCCCAGCCCCACCCCGAGCGCTGCCAGAAGGGGAACGTGGTGTTCATCAGCAGGTTGCCGCCGGCGCCCAGGTTCTTGACCTGCGCCTGCATGCTGGTCACTACGGCAGCGTCCGCCTTGCCGCCCAATGAGGCCTGCACGCCGTCGACCCGCCCGGATAGTGCGGTCAGCTGCGTACCCTGCTGGCTGACCTGGCTTTTCAGCTGCGAGAAGCCGCTGGCCGAGACGTCGCCCACCTGGGTCTTGAGCTGGGTCAGGTCACGCGCCGTGGTGTCCAGCTTGCTGCCCTGCTGGCTCACCGAGGTGCTCAGCCCACTGATGGCCGAGGCATTGGCATCGTTGGCCACCTGGTCGGTGATGTCGTAGACCTGGACGCTGTCCACCCGCACCTGGCCGTTGTCGGGGTGAGCATAGATGTTCAAACGCCAGGCATCGATGCCGCTGTTGAAAGCATCGAAGTCGAACGATCGGGTCTCGAACGCCTCTACTGCGAACACCGCACGCAGATCCTGATAGGACTGCTGGCCGGCCGCATTCTTGCGATAGATCCGCACCAGCAGATTGTTGGCACCGCCAGCACCGCAGGCGCGGACGATCACCCGCAGGCGGCGCGCGCCGTTGATCGGCACCCATTTGCCACCGTTGGCCTGCAGGGTCGGATTCACGTTCGTGTAGCGGTTGAGCAGCACACCTGGGCGTCCATCACCGTTGACCGTGCTCCACACCGCGCCATTGGCGGCCGCCGATGCCGTCCAGCCACCCAGCCCTTCGGCGAAGTCGGGATTGGGCAGCAGGCCGCTGCCGGTGTTGAGTACGCCCTTCAGCCCACTGGACAGGTCGGTGATCTGCTGAGCCTGCGCATCGACCTTCGCCCCCTGCTGATCAACCTTGGTGGTCAGCGCGGTCACTGCAGTGGCCGCGGCAGCGGCGCTCTGCCGCGCGGCGTAGGCGTCGGTGACATCGATCATGCGGATGTCGTCCACCTGCACGCGCACGCCCACTTCGCGCGCACCGCTTCCTCCCGGGATGCTGACCAGCATCCGCCACTTCGCCGCAGACGCGGCGGTATTCATGTAGCCGCTGACCTTGGTCCAGCCATCCTTGCGCAGGGAGGCCAGTGCGTAAGCCTGCAAGGGCCACGAATTCTCCGCGTTGGCTTCGTTCGTGGTCTGCCAGCCCACCCGGATCGAGCCACCGGTCGGCTGGATGCTGTCTGGATGCAGGCGTGCGTAGTACTCCACGTAGATGCGGCGATTGCCGGTGATGGGGGTCCACTGCCCGAGATACAGGTCCGCATTGGTGTTCGGGCTGGTATTGGCCGCAACATTCACATCCAGACCACGCTCACCGGTCCGGCGAGCATCGGCGCGGGCGGTGTAGATCGTGCCCGCCGCACTGCCCAGCAGCTGGCCATCCTGGAACGTTTCGAACCCACCCAGCGGGAACAGGCTGTCGCTGCCATTGAGGACCGATTGCACGTCCGACTGCAGCTTGACCACATTGGACGCACTACTGGTGACACGATCGCCAAGCTGCACCACGTCGCTGCGCAGGTTGGCGATGGCCGTCGCGTTGCCCGCGATGTCCTGCGCATCGGTGATGTCGTAGAGCTCGATCCGGTCAAACAGCACTTTGCCGCCGGCGTTGGTCAGATGCACCTGCGGCATGATCTCGTTGCGATCCTGCGCGGCAGACCATTCGGCAGAGTAGGTTTTCCAGGCCGCATCGGACAGGTTCAGCGTCACGTCGGCGTGGCTTTCACTCACCCCGCTGGTCCGCACGCGCAGCCGGCAGACCAGGGTGGCCGTCGCATTGTCGAAGGCGCGGGCGATCATCACCAGGCGGTACCGCCGCGACCTGCCGGCAACCACCGGCAACCAGCGCGCATCATTGGCCGTGATGAAGGGGTTCTGCCCGGCCTGGGGACCGTGTGTCATCAACAGTGCGTCACCACTCTGGCCCGATGCTTTCACCCACTCCACGGTGTTGGCCGACACGGTACGGGTCAACGTCCACCAGGCGGCACTGCCAGCGAAGGAGCTGTTGCGCAGCACGTTGTCGCTGCTGGTCACCGAGGTCTCCACGCGCGCGGCCAGGCTGGTCAGGCTGTCGGCCGCTGACACCAGGTCGGTACCGAGCTTGCTGACGTCGGTGCGCAGCCCAGTCAATGCTTCCGCATTGCTCCGCGCCGTACGATCGAGCATCGACGAATCCTGCGATCCGGTCGGCACGCCATTGAGCACGGTGACGGTCATTTCCACCCACATGCCGGTACGGCCGGTCTCCGGCAAGGGCGACAGGATCTGCCTGCCACCGCCGGCACCGCTCCTGCGCCGCCCGATCATCACCAGCATCCGCGACCCCGACAGGGCCGCCAGGTTCTCCTGTGACAGGCCCGCGTCCAGCAGGCGGGTGCGCAGCCCACTGGTGTCGGTGTTGCTGGCGCTGCTGATCGCCCCCACTGCATCGGACGTATAGGCAATGAAGTACTGATTGTCCTTCAGTGTCTGGTCGTACCAGGTGTTGAAACGGGCCGACTCGCTCTGCAGGTTGCCATGGGTATCGAACACCGCCGTATCGGTGATGCTGTTGTCCGCATTGATGATGCCGACCCGCAGCCCCCGGTTGGCGCCCATGCCCGGCACGATGCTGCCATTGGCGCGGTATACACCCGATGCGCGGGGGCCACCCGTGGGCGAGGACGCGATATGTGCGTTGGCGATGATGTTGTAGGCCACCATGTTGCCGATGCCCGAGGCCAGCCGCGTGACGTTCTCGGCGGCACTGGCCAGCTTGCCATCGATCTGTTCCACCTTGGTCGACAGGCCGCTGACCGCCGTAGCGTTCGCGTCGACATCGGTTACATCCTCCACCCACAGATCGTCCAGCCACAACGTGCCGGCCGTACCGTTGCGATTGATCGTGACTCTGATGCCCTGCACCGTGCCCGTGGGCGGCAACGTCACGAAGGTCTCGGTCTTGACCCAGTCGGCCGATTTCGGGAACGACTGCGTTGCACCGCCCATCAGGTTGCCGTTGTGGTCGGCGACGCGCAGCTTGGTGTTGTCGGCGGTGCCGTCGAAGTCCTCGCTGGTCCGCGTCCAGCACGACACTCGATAGCGACGGCCGGCGGTCAGGGTGATGACGCGCCCCTCATTGACCGCGGCGCTGACCACCGTATTGCTTCCCGCTGCGTAGGGCTCCGCCTTCCAGCACAGACTGTTGCCGCGCCCCTCGCGCACCACCGATGCTGCGGTGGTGTTGAAGAACGTCCAGCCGGTGCCAGCGCCCAGGTTGAAGTCGCCATTGAGCGCGAGGTTGCTACCCGCGCCCATCACCGCTTCCATGCGACTCTTCAGTTGCACCAGGTCCTGGCTGCTGCTGGTAACCCTGCCATCGAGCTGCCCGACTTCGGTCTTCAACGCATTGAAGGCGCTGGATCCGATCTTGTCCCCCATCGTGGCATCAAGGCTGTCCACGCGCCGACCCAGCGCGGTGTCAGCGGTCACCATCGCCTGCTGCAGGCTGCTGACACTGGCACTGGTGGCCAGCGCACCGGTGCCTGCCGGCATGCGTGCCTGGAGTGCCTGGATCGACTGCGCGTTGACCTGGTCGCCGCTCAGCCGTGCGGTTTTCTCGGCCGCGATCAGGCCCTGGCTGACCCCCGCCAGTTCACCGCCCTCGTAGCTGCCGCGCAACTGCACGGCCAGCGACTCGCGCCGGCCCGCTTCGGTGCTGTCTGCCGCTACGCGTGCAGTGGCTTCCTCCTGCAGCATGGCCACCGACGCACCCGGCGTCGGGCGACCGATCGCCACCCAGTCCAGCAGGAAGTAGTGGGCGTCGGTCTGCGCCTTGGACAGGTCCAGGCGGATCTGGTCGACGACGGTACCGTTCCATGGAATGTTGTCCACATCCAGCGTCGCGATGCCGTTGCTGTCATAGCTTGGCTCCGCGAACTGCACCATGCGTGCGTTGTCCCACGACTGGCCGGGACCGTTCCACAGCAGGCGCCCGTCCCAGGCAGGACTGCCCACCTTGCGGATGCGCAGCTTGACGAAGCGATGCGCCGCGCCTTGGACATCCTGGCCGCGCGGGCTGGTCACGAAGGCATCGCTGGCATGGTTGGCCGGGCGCAGCCAGCCCTCCACCAGCGTTGGACTGCCACCGTTTGCCCCCCACCCTTCGACGCTGCTGTCGAAGTACCAGATGCGCTTGCTGTCGAACTGCACGCCACTGCCCGCCGACAGCTGGCTTACCATGCGGGTGAGGTTCTCCACATCCGACCGGCGTTCGCTGGTTTCGCGGGTCACCGCCGTGGTCAGCTCGGTGCGGGTATTCAGATCGCCGGCGGCGCGGTCCAGCACTTCGCGTGCAAGGCCATCGGTGCTGGCCTTGAGCGCCAGGGCCTGCTGGTCCAGCCGTTCGGCCTGGCCGGCAAGCCGTTGGGCGCTGGCGGTGATCTGATCCTGCAGGCGCAGCGATTCGCTACGCAGCGCCTCGGCGGCACGGGTGGCGGCGGCCAGGTCGCTGTCAATGCGGGCGTTGATTTCCTTGCCCAGGTCCTCCTTGACCGATTCGACCACACCGCCGATTCCCTCCAGCGTCTGCCCGGTGTTGCGCCCCAGCGAGCGCCGCAGGTAGCGGGCACCGACGGACAGCACGCCGGCGGTGTTGCGGCTGCGACAGGCAAACGTCCAGCTGCCCGCCTCCGGCAGTACGGCTTCGATTGCGGAGGTGAAGAAGCCACCGGCATCGCCCAGCGGGGTCATGTGCTCCCACAACGGGTTGTCGATGCTGCCGGCGGTATAGCGGATCTCCACGCCGGCGAAATCAGCCGACTGCACGGTGTCGCTGGAGAAGCCCCACACATAGCGGCGCACGCCACCGCTGAGCTCTTCGATGTCGAACAGATCGACCAGGACCGGCGGCGCATCAGCACCCAGCGTGGTGTACTGGGTGGACACGGCAACGCCGGCACGGCCATCGAGGCTGTACGGACGAACGACCACCGGATAGGTGCCCGCTCCGGGAATCGCCCAGCTCGCCGACCGCGTGCTGGTGCGTGCCACTTCCTCCAGCGCAGCATTGCCGTCTGGATCGGACAGGACCCGCGTTTCGCCGGCCGGGCCACTGATATCGAAGCTGGCCTGCAGTTCGGTGTGCATGCTGCCGCCCCGGCTGACCTGGCGCTCGACCACCTTCAGATTGCTGGCCACCGGCCGGGTCTGCAGCGAGGATTCATTCGACGGCGGCACATACTGGCCGGTCCGCACGTAGTGCCAGAACTCGGGCCCCTCCTGCACCACCTCCACTGCGGCGCCCTTCAGGTCGCCTTCCGGGCGGATGCCGGTCACGCGCACGCGGGTACCCGGCGTCTGCTTGAAGTCGTAGATCCAGATCGTGTCGTGTGCAGGATTGCCGTCGTTGTGGCCCGGCAGCGGTGCATCTGCCGGCCAAGGATCGGCCAGCACCAGCCTGTCACTTGGCTCCGTGCCCGGAACCACGCGCAGTACGCGGTAGACACGCTCGCCTGGAATGCGCAGGCCGATGAACGCACTGCCCAGAGAGGGTGCCGGGACCGTCTCGTCCAGTTGCAGCGTGGCAACGCCTGCAGCGTCGACGGCGGCACCGATCAGGCGGCCACCGAAGCCCCACTGGGTCAGGTCGTGCTGCAACGCCAGCACCGACAGCCGCGAGTAGGCCAGGTGTTCGATGTCGGTGCTGTAACTGATCGACTTGTACTGATAGACGCTCTGCGCCAGATGCCAACGCGCCAGCATCGCGGCATGGGCTTCGGAGCTGACGCCCTCACCGGTGATCTTGGCTGGATTCAGCATCACCTCCACGCCCGGCGCCGGCACGCGCAGTGTCGCCGCCTTCCAGGTGCGACGGTCCAGATAGCTGTACTCGATGCCGTCGGCAGCATTGGCCAGGGTGTAGTCAACCTGGAACTGGCCCTTCTTGATCGTGGCCATGTTGACCACGCCGGAAAGGGGCTGCTCGTCGGCCGCCCAGGCCACGCCCAGCCGCCCCTTGGCCCAGGTCACCTGGCCGAAGCCGGCCAGCGCGATGGCGTCGAGCACTGCCTGGTGGCTGCGTACCTCGGTCAGCCAGTAGTCGTAGCCCAGCGCGTTGTCCGCGCAGTGCAGCATGAAGGCTTTCAGGCTTTCGATATCGATGCGCCGATCGGCCATGCCCAGGCCGGCGATGCGCTTGCCGTTCTCATCATGGATGCCACGGGCGTAGGCCAGGATCTGCGCGCCCGGGTTGCTGGTTTCCTCGGTCACCCAGCCGGCTGCTTCGCCCTTCCACACAGGAATCGGCCGCGCATGGGCCACGCAGCGGATTTCATCCGGGGTGCCATTGAGCTGGCCGGACGCCTTCATCTGCAGGCCGATGGCAGGAATGCCAGCATGGCTGGCGTCGTCGCGCTGCACGCTGACCAGCGTGGTCCAGGTGAAATTAGCCTGCGCGCCACTGCCATCGGTGTTCTGCCCGGCCACGCGTACGCGCACGTCGTACTGGCCCAGCTCCACGTCGCGGCCGTAGCTGACGCGACGCGCCTTCTGCGTGCGTCCCACTACGCTGTAATTGCCGAACGACTGCCAGGCATCGGAGCCGACCGGCCGGTACTGGATCTGGATCTGCTCGCGGTTGTCCTTGTCCTTGCCCTTGGACGTGGTATCCCACAGCCGGAACTCGATGTTCACCTGCAGGCGCAGAGATTCAGCGGAACTGGTGCGTTCCACCCATGGGCTGGCCATGTGCTTGGCATCGCTGCCGGTATCGAGCAGCTGCGCACCTTCAATCACATCGGCGTTGCTGTACAGCGGAATCGCTTCGTCGGGCATCCGCGGGAAGCCGCGGAACCAGGTGCGCACGCCCTCGTAGCTGGACAACGCCGAATCACCGTTCTGCAGGGCCTCTACACGGCCAACGTTGATGCCCGGGCTGAGGGTCAGGCCGACGTACTGCTCATCGCCTTCGAACCAGGTATAGGGGCGGCTGATCAGGTCCGGCGCGAGGCGCGTGGAACCGAACAGCAGGCCCAGCGGTTCATAGGCGCGCACACGGTTGCGCGGCGCTGCCAGCGAATACGCAGTGTCGGCGACACCGCCGCCACCACCCGCACGGGGAGGCTTCGGGCCCAGCACCTTGTTGATCAGCACGCTACCGGCTACGTATACCGCCGACGCCAGCGCGGTACCGTAGGTGGCGCTGAGCCCCGCAACGGCGCCTGCCCCCCAGGCGGAACCGGCCACCAGCGTGCCGATGCCGAAGGTGAAATAGGTCAGCGCGATCATCGCCACCAGCGGAATCACTGCCTTGCCCACCACGCTGCGCACTTCGATCAGCTGGCCATGGCGCGGTCGCACCTGCATCCACTGCTCGCGCGGCACCTCCAGCCCGTCCACGCAGACCTGCCATGCGCGGCCATCGAGCCCGTCTACATGGCGCATGAGGAACGCGTACAGGCTTTCACCCGGGCGCAGGTCGACCGGCACGTTGCGCTGGCCATCCAGCAGCACTGGGTGCGGGGTGATGATGAGGCGGCCGTCGACCGCCGGTTGTGGTGTCAGTTCCATGCGTAGTATCCCTCGATCCTCAGCCCAAATCCGGGCAGGTCACGAACGCGGTGCAGCACGCTGCAGCCGTTCGTTTCGTTGCTGTGCAAGACCCAGCCCTCATGGGCCAGGAAAAAGAAAACCCCGGCATGGCCGGGGTTGTGTTGTCCGCGTTCGATCATCAGTACCAGGTCGCCGTCCTGTGGAGGGCCCTCGCGAGGTACCGCCTGCGCGCGCGACAATGCGCCCAGCTCGGCCGAGCCGCGCCGCCCGCGCGGCCGGCGTCCGGGCAGTGCCACTTCACGGGCGAACAGCGCTCGCTGCACCTGCATCACCAGGTCGGCGCAGTCGTACGCCGCTTCGTCATAGGGGATGCCCACCCATTGCTCGACGTCGACCAGGCGCATCAGAAAATTCCCGGCAACGTGAACGGATTGGCATGCAGCAGCACGGCCTGCTGCCGCATCAGGAAGTCGACACCACACTGGGCACTGACCGTGCGCGTGTTGACCGACACCTGGGTCATCGGCAGGTCGTACTCGGCCTCGATGGCATCCGGATCGGCGCGATCGGTCAGCATCAACCGTGCGGTCACCATCTCTCCGGGGGCCAGCCCTTCCAGGTCCTCGGTGAGTGCGCGGCCGATGTTGTCGATCACCAGCTGCGCGCGCGGTGCCTGTCCACTGACATCGTCGGGAAGCTGGAAGCCGAACGGTGCGGCAATGAACTCCCTGCCGTTGCTGGTCCAGTTGACGTTGTCGTTGACGATCCGCAGTACCTCCGGCATCGACGGTGCCGACACTTCCAGCAGCATCAGCGGTCCCTGGGTGTCGGCCAGGCGCTGGCGGCGCTCATGGAACGAACTCATCGCATGTACTCCAGTACAAGATCGCGCTTGGAGAAGCGGAACCGGGTGTTCAGTGGCACCAGGCGGCCGATGCCCTGCGGGAAGCGGGCGCTGATCGGCTGCCCGGTCCGCGGGTGCTCCATCGTGAACCAGCCGACGCGACCGACATCGTGCAGGTACCACTCTTCGAATGCCTCGGCGTCAGCCGCGGTGCGGAACTGCACCGAGGCGTACACGTTCTTCATCACCCGGCTGTTGAGCGCGCGCATCTTGCTGGGGCCGCGCTCCATCTCGGTCCGCTCTTCCGAAGCGACGATCTCCTCGCCGTAATCCGCAAAGCGGATTTCTGCATACTCTGGCCAACTGCTCATCCCACTGCCTCCGTCCATCCGTATCGGGCCCGTCCAATGGCGCCCAGCTCACCACCGTTGAGGCTGTCGCCCACGATGTCGATCACCAGTCGCCGCACTTCGCTGCCATCGGGCATGCGCTGTCGCTCTTCCCGGGTGTTGACCCGGCTTTCGCCGTAGTTGTTGATTTCCACATTCATCCCACCCTCGCCGGCACGGGCGATCGGCACCTGCACGTATCCTCCGCTGTCACCACCGGGCAGGCCGTTGCCGCTTCGCAGCGACGTGCGCAGGGCAAAGAATGCCGATGGGCCACCGAGCGCGGCCATGTCTTCCTGGCTGAGTACGCCCTCGCCCTTGTGGACGATGCCGGCCGGCTCGTACTTACCCCCCGGGCCGGTGTAGCCGCCGGCGGAATACACTATGTCGATGGCCTCTCTCTTCACTGGGCCAATCTGCTGGTTGAAGAACGTGTTGAAGATGCCCACGATCGCCTGCTTGGCGGCAATCCTTGCCAGATCAGCGATGATGGAATTGGCCATCGTCGAGAACGACAGCTTTCCAGTCTGGGCAAACCTCACCAGACTCTCCTCCATGCCCGAGAACATGTTGGTGAACAGCCCACCACTGGCCTCGGCCAGATTGGCCGCACCCGCTGCATAGTCTTCGAATGCCTTGGTGGCGCCGGCACTCCAATCGGATTCAAGCGCCTGCTTCGCCTGCTGGAAATCAGCCTCACGCTGCAACGACTCCGCATGGAATGCGTCCAGTTCGGCGAGCTTGCTCTTGTAACCGGCCGACTCGATGACCTTGCCGTCTTCTCCACGTGACTCGTCGTCCAGCGCACGCTTTCGATTCTCCCGGTCCTCATCCAGCGCGGAACGGCGGTGCATGCGATCCACGCTCGCGGCGCCATGGCCGATGCCGAACAGTGCCTGGTCGTTGCCGCGCTGCTGTGCATCCGCCGCCTGCTGGAGCTCCCGCTGCAGCTTCAGCAGGTCCTGCTGGGCTTTCTTCGACGCTTCAGCGGCTGCCGCTTCCTTGGCCAGGGCCACGGCGGCGTCCAGCGAGGCCTTCACCCGCAGTTGCTTCTGCTCGCTGAGCTTCTTCTCGGCATGCTCCATCTCATCAAGGACGGTGACCTGCAGCTTTTCCGCCTCTGTCATCCCCTCCTTCAGCTTCTGGCGCACCCGGTCCTGGGCGATCTGCTTCTCGATGCGATCCATCAGCCCGGCGTACGCATCAGCCTGCTCGTTCACGCCCCTGACCGACTGCTGGGCAGCCTGCTGCTGTTCGCGGAACTGGGCCTTGCGTTCGATGTCGGCCTTCTTGCGCGCGGCGTCCCTGTTGAACTCGGCGCGCTGGGCCGGGTTCATCTTGTCCGGGCCACCGTTGGCGTTGATCTCCGCACCGCGCTCAGCCATCCAGGCCGCATATTCGCCACGGGTCAGCCGGATCCACTCGACCTCGTCCCGCCACGCTTCTCCGCGCATGCTGCCCAGCATGCCCGAGATCGCCGAACCGGCCTGCAGCGCCTCCCAGCGTGCCGACCCCAACTCAGCCTTGAACTGGGCCAGGGTTTGGTTGTCGAGATTGTTGACGGCATCCTGGATCCGCTTGAACAGCTCTGGATCCACAGAGTTGCGGATCTGTTCCTGCAGTGCCTCGAACTGGCGCCGTACAGGATCTGTCTTGCCTTCGAAATCCTGCAGGGCGTCCTTCGCGGCCTTCAGCCCTGCGTAGTCGGCCCCCGCGCTCATGCCGGCGCCTTCCCGTGCCGACTGCTGGCCGTAGGCCACGCGTCCTTCCCAATGGGTGACTGACCCTTCCAGCGCTCGCTTCTGCGCTTCGAGCTCACGCATTGCCTTTGCCTGCTCATGGAGCGCAGCGACACCGGCTTCTATCGGCAGGCTGCGATCCCGCAGACCCTTGCCGACTTCATCCATCGTGAACGACATCAGCTTCAGCGACTGCATCTGTTCGTTGAACTCGGCGCGCGCACGTTCGGACGCCTTGACCATGTCCAGATACGCTTCGCCCAGCTTCTGCACCGACGCAATGGCAATGCCCCAAGGGCCGCCGGCGGCCGTCAGCAGGCCGCTGCCCAGCTCCTTCAGGCCGCTGCCCAGCACATCGTCGCCAGCGTTGGCCTTTGCCTTTGTCCCGGCCTTGACTGCCGCGCCCTCCGGTACCGCATGCACGCGTGCCAGCGCGGCGGCCGTCCGCTCGGCCTCCGCGCGCAGTGTCTTGAGATTCTGCGTCGCCAGGCGACTGGCCTCCGCCATTGCGGCACGGAAGCCCGTCGTGTTGACCCGCAGTACTACGTCTAGATTCTGGTTAGTGGACGCCATACGCGTTCCTCCAAGAATGATGAGGGGCCCCGCAGGGCCCCAGGTTCGATTGCATGCCACGCATCGGAGAAGCACTGCCCTGCCCCGCCCGGAATCACGCCGCAGCGTTGCGTCGCGATGCGCTGCCGAACAGTTCCAGCAGCTGCTGCGAGCGCTCCTTTGCCGCCCCCTCCGGCGACGTGCGCGGCCGCACCAGCAGGAAGTCTTCGGCAGTGGTCGTATTGCCGTGCACCTGCGCCAGCACGCTGGTCAGCTGGGCTAGCATCCCCTGCAGGGGCTGGTCCAACGGCTCCAGGCGTGCGAACGCATACATCTCCGAGAGCTGGCGGGAGGTCACTCCCGCCAGCAGGTGGTCCGGATGCGGGAGGCCCAGCCTCCACGCGATCCGGAACTGAAGCCGGCGCTCAGGCCGGCGGATCAGTTTTTTTCCAGCTCTCCCACGGCCGCATCGCCGAGCGCATTGAGCGTCTGTGCGACCCGGAACACGCGATCCAGCGCCGCGGCCGATTTGGTGCCCAGCCGGGCCACCTCATGGTCGGAGAACAGGCGCTCGCCCATTTCATCGACCAGGCACAGGCCGACGAATCGCGCACGGAAGTCATCCACCTTGGGCGTGTCACCGCCGTAGGTCTCCTGCTCCCAACGATCACGGTCACGGGCCGACATCATCGCCACGCGCACGCTGCCACCCCATTCGGGTACGGCGACGTCCTCGTGCCGGCGATCCTGTGCGTCCAGGATCTGCTGCTTGCCCAACAGCATCACGGGGTGCCGCCAGCGGCCACGGTGACCAGCGCGAACTCACGCGGCAGCAGGTCCGCAGTGAACGTCAGCACCTGGTTGGTACCCGGGGCCACGTTGAAGGCGGCGACCTTGGCGACGAAGGTGGCCGCATCGCCGGTGGGCAGCACCATCAGGAAATGCAGGTCGGCATCCGGATCGGCGTCGCGCAGGATCTCCTGGCCTGCCGAGCTGCCGACCGGCCAGCGGTGGCCGGACACCTGCACGGCCTGGCCGCCGGACAGGCCCGCGATGTTCTCCATCTGCTTCGAACGCAGGTTGGTGGCATCAAGGGTGTTGGCCTGGCCGCGGCCGAACGGGAAGGCAGTCAGGCCGTCGATTTCGGTATAGCCGGCCGGATTGTTCGGCGCGGTCGGGGCGGTGCCGGCCTTCACGTACAGCGCGGAGTCCTGGGCGGAAATGGCTTGATTGATGGACATGGTGTTGAATCTCCTGGAAATGAAAAAGCCGCCTTGCGGCGGCCGGGGTTCGGGGTGATCAGGCTCGGGGCTGCCTGCAGTGGGTCATCGTGGCTGGCCCGTCACAGCCACCGGTTGCGCGTTGCGATCGGCAACACGCGGACAACAAAAAAGCCCCCGGCTCGCGCCGGAGGCTTGTATGTCATCGTGGCTGAAAGCTTAGGCTGCGGGTGTGCACCGGTCAATGCAGAAACAGCCCTCTGCACCGCCTCGGGAACGAACTACCGCAAGCCCGCAGCCGCCCGATCCGGCACAGCCGCTGACGCCACGCTAACCGGCGCAGCACCGACAATGCAGCTCTGTTCCCAGCAACGAGGAAGACGACGATGGCCGAGTGGATCACCCTGGATACGCATCACGGCCCGGTACGGGCCTGGCAGGCCCTGCCGGAAGGCACCGCGCGCGGTGGCCTGGTGGTGGTGCAGGAAATCTTCGGCGCCAATCCGCACATCCGCAGCGTGGCCGAGCGCTTCGCAGCCGAAGGCTATGCGGTGCTGGCGCCTTCCTTCTTCGACCTCGTCGATGGGCCCGACGCCGACCCGGATGCCCTGCCCTACGACGCCGAGGGCGTGAAGCAGGGTCTGGAACGGGTCGGCGCGCTGGGCATGGAGCGGGCGCTGGAGGTGGTGCGGGCCGCGGCAACCCGGCTGGCGCCGCAGGGCAAGGTCGGCACCGTCGGCTACTGCTGGGGCGGCACGGTGGCGATGCTGTCCGCAGTGCGCCTGGGGCTGCCGTCGGTCAGCTACTACGGCGCGCGCAACGTGCAGTTCCTCGACGAGGTGCCCAAGGCCCCGGTGATCTTCCACCTCGGCGCCCAGGACCGCAGCATCCCGCCGGAAGCGGTCCAGGCCCACCGTGAGAAGCTGCCGCAGATGGCCACCTACGTCTATCCAGCCGATCACGCCTTCAACCGGGAGGTCGGACATGCGTATGATCCAGACAGCGCCGCCCTGGCGCTGCAACGCACCCTGGACTTCTTCTCGGAGCATCTTGGATGAGCGAATTCGAACTCGATTCACGCCTGGCCACCGATAGCGTGCTGGTGGCGGAAGGACCGTTGTCGCAAGTGCGGCTGATGAACGACGAACGATTCCCCTGGCTGGTGCTGGTACCGCGCCTGGCCGGGGTAACCGAGTGGATCGAGCTGGACGGCGAGCAGCAGGACAAGCTGCGCACCGAGCTCAACCGCGCCTGCAAGGCCCTGAAGGGCTCCGACGGGGTGGAAAAGATCAACATCGGGGCGCTGGGCAACATCGTGCGCCAGCTGCACTTCCATGTCATCGGCCGCCATGACGGTGATCCGGCCTGGCCGGGCCCGGTCTGGGGCAGCGGCCCGGCGCACCGTTACGAGCCGGCGGCGCTGGACCAGCATGTCGCCTACTGGAAGGAAAGGCTAGGATATCCGGCCCAGTCCTGAGCCTTCGCCGACCCGATGCGATTCAACCTCGTTGCCGCCGTCCTGCTGATCCTGATCGGCCTGTTCATGCTCGCCAGCAATCTCGGCTGGACGCACCTGAACCTGTCCAAGCTGCTGTTGACCTGGTGGCCGGTGGCCCTGGTGGGTGTCGGCATCGCGATGCTGTTCGGTCGCGGGAAATGAGGTAGCGCCGGGCCATGCCCGGCGAGCGCAGCGCGCGGCCCCACAAACGGAAACGCCGGGCATGGCCCGGCGCTACCGATACGCGCTGACGCAGGCAGTCAGGTCCGCGGCAGGGTCACGCCGGTCTGGCCCTGGTACTTGCCGCCACGGTCACGGTACGACGTCTCGCAGATGTCATCGGCGGCCGCCTGGAAGAACAGCATCTGCGCCACGCCTTCGTTGGCGTAGATGCGCGCCGGCAGTGGCGTGGTGTTGCTGAATTCCAGGGTGACGTGGCCTTCCCACTCCGGCTCGAGCGGCGTCACGTTGACGATGATGCCGCAGCGCGCGTAGGTACTCTTGCCCAGGCACACCACCAGGGTATCGCGCGGGATGCGGAAGTACTCGACGGTACGCGCCAGCGCGAAGCTGTTCGGCGGAATGATGCACTCGTCGGCGGTGATGTCGACGAAGCTGCCCGAGTCGAAGTGCTTGGGATCGACAATCGTCGAGTTGATGTTGGTGAACACCTTGAACTCGCGCGAGCAGCGCACGTCGTAGCCATAGCTGGACGTGCCATAGCTGACGATGCGCTGGCCGTTGGCCTGCTTCACCTGCCCGGCCTCGAACGGCTCGATCATGCCGTGCTGCTCGGACATGCGGCGGATCCAACGGTCACTCTTGATGCTCAT

Protein sequences of DBSCAN-SWA_4

>NZ_CP021768|3138163:3153509|3138163_3146452_-|WP_087923216.1|tail|DBSCAN-SWA
MELTPQPAVDGRLIITPHPVLLDGQRNVPVDLRPGESLYAFLMRHVDGLDGRAWQVCVDGLEVPREQWMQVRPRHGQLIEVRSVVGKAVIPLVAMIALTYFTFGIGTLVAGSAWGAGAVAGLSATYGTALASAVYVAGSVLINKVLGPKPPRAGGGGGVADTAYSLAAPRNRVRAYEPLGLLFGSTRLAPDLISRPYTWFEGDEQYVGLTLSPGINVGRVEALQNGDSALSSYEGVRTWFRGFPRMPDEAIPLYSNADVIEGAQLLDTGSDAKHMASPWVERTSSAESLRLQVNIEFRLWDTTSKGKDKDNREQIQIQYRPVGSDAWQSFGNYSVVGRTQKARRVSYGRDVELGQYDVRVRVAGQNTDGSGAQANFTWTTLVSVQRDDASHAGIPAIGLQMKASGQLNGTPDEIRCVAHARPIPVWKGEAAGWVTEETSNPGAQILAYARGIHDENGKRIAGLGMADRRIDIESLKAFMLHCADNALGYDYWLTEVRSHQAVLDAIALAGFGQVTWAKGRLGVAWAADEQPLSGVVNMATIKKGQFQVDYTLANAADGIEYSYLDRRTWKAATLRVPAPGVEVMLNPAKITGEGVSSEAHAAMLARWHLAQSVYQYKSISYSTDIEHLAYSRLSVLALQHDLTQWGFGGRLIGAAVDAAGVATLQLDETVPAPSLGSAFIGLRIPGERVYRVLRVVPGTEPSDRLVLADPWPADAPLPGHNDGNPAHDTIWIYDFKQTPGTRVRVTGIRPEGDLKGAAVEVVQEGPEFWHYVRTGQYVPPSNESSLQTRPVASNLKVVERQVSRGGSMHTELQASFDISGPAGETRVLSDPDGNAALEEVARTSTRSASWAIPGAGTYPVVVRPYSLDGRAGVAVSTQYTTLGADAPPVLVDLFDIEELSGGVRRYVWGFSSDTVQSADFAGVEIRYTAGSIDNPLWEHMTPLGDAGGFFTSAIEAVLPEAGSWTFACRSRNTAGVLSVGARYLRRSLGRNTGQTLEGIGGVVESVKEDLGKEINARIDSDLAAATRAAEALRSESLRLQDQITASAQRLAGQAERLDQQALALKASTDGLAREVLDRAAGDLNTRTELTTAVTRETSERRSDVENLTRMVSQLSAGSGVQFDSKRIWYFDSSVEGWGANGGSPTLVEGWLRPANHASDAFVTSPRGQDVQGAAHRFVKLRIRKVGSPAWDGRLLWNGPGQSWDNARMVQFAEPSYDSNGIATLDVDNIPWNGTVVDQIRLDLSKAQTDAHYFLLDWVAIGRPTPGASVAMLQEEATARVAADSTEAGRRESLAVQLRGSYEGGELAGVSQGLIAAEKTARLSGDQVNAQSIQALQARMPAGTGALATSASVSSLQQAMVTADTALGRRVDSLDATMGDKIGSSAFNALKTEVGQLDGRVTSSSQDLVQLKSRMEAVMGAGSNLALNGDFNLGAGTGWTFFNTTAASVVREGRGNSLCWKAEPYAAGSNTVVSAAVNEGRVITLTAGRRYRVSCWTRTSEDFDGTADNTKLRVADHNGNLMGGATQSFPKSADWVKTETFVTLPPTGTVQGIRVTINRNGTAGTLWLDDLWVEDVTDVDANATAVSGLSTKVEQIDGKLASAAENVTRLASGIGNMVAYNIIANAHIASSPTGGPRASGVYRANGSIVPGMGANRGLRVGIINADNSITDTAVFDTHGNLQSESARFNTWYDQTLKDNQYFIAYTSDAVGAISSASNTDTSGLRTRLLDAGLSQENLAALSGSRMLVMIGRRRSGAGGGRQILSPLPETGRTGMWVEMTVTVLNGVPTGSQDSSMLDRTARSNAEALTGLRTDVSKLGTDLVSAADSLTSLAARVETSVTSSDNVLRNSSFAGSAAWWTLTRTVSANTVEWVKASGQSGDALLMTHGPQAGQNPFITANDARWLPVVAGRSRRYRLVMIARAFDNATATLVCRLRVRTSGVSESHADVTLNLSDAAWKTYSAEWSAAQDRNEIMPQVHLTNAGGKVLFDRIELYDITDAQDIAGNATAIANLRSDVVQLGDRVTSSASNVVKLQSDVQSVLNGSDSLFPLGGFETFQDGQLLGSAAGTIYTARADARRTGERGLDVNVAANTSPNTNADLYLGQWTPITGNRRIYVEYYARLHPDSIQPTGGSIRVGWQTTNEANAENSWPLQAYALASLRKDGWTKVSGYMNTAASAAKWRMLVSIPGGSGAREVGVRVQVDDIRMIDVTDAYAARQSAAAAATAVTALTTKVDQQGAKVDAQAQQITDLSSGLKGVLNTGSGLLPNPDFAEGLGGWTASAAANGAVWSTVNGDGRPGVLLNRYTNVNPTLQANGGKWVPINGARRLRVIVRACGAGGANNLLVRIYRKNAAGQQSYQDLRAVFAVEAFETRSFDFDAFNSGIDAWRLNIYAHPDNGQVRVDSVQVYDITDQVANDANASAISGLSTSVSQQGSKLDTTARDLTQLKTQVGDVSASGFSQLKSQVSQQGTQLTALSGRVDGVQASLGGKADAAVVTSMQAQVKNLGAGGNLLMNTTFPFWQRSGWGWGSNPNGRWSELGNPTGDDSWHPKGITGLGSVTPGVVAAGEIAWWGTEYDIAIEGGKTYCASAWINTHRVEVKLEMTFFDAAGNHLGLVHSPGVRSDTGTPITLDRLTRTFLITKAPATASFARFRVIVIGTGGTTPYFWMFRPMLSQVDASATAPPTWSAGGTESSAQWSVNVRADGRVGGVQLASSGQVSRFDVVADAFSVSAPGGGRRTEYSDGNWRVYDEAGRLRVRMGVW
>NZ_CP021768|3138163:3153509|3147645_3149979_-|WP_087923218.1|tail|DBSCAN-SWA
MASTNQNLDVVLRVNTTGFRAAMAEASRLATQNLKTLRAEAERTAAALARVHAVPEGAAVKAGTKAKANAGDDVLGSGLKELGSGLLTAAGGPWGIAIASVQKLGEAYLDMVKASERARAEFNEQMQSLKLMSFTMDEVGKGLRDRSLPIEAGVAALHEQAKAMRELEAQKRALEGSVTHWEGRVAYGQQSAREGAGMSAGADYAGLKAAKDALQDFEGKTDPVRRQFEALQEQIRNSVDPELFKRIQDAVNNLDNQTLAQFKAELGSARWEALQAGSAISGMLGSMRGEAWRDEVEWIRLTRGEYAAWMAERGAEINANGGPDKMNPAQRAEFNRDAARKKADIERKAQFREQQQAAQQSVRGVNEQADAYAGLMDRIEKQIAQDRVRQKLKEGMTEAEKLQVTVLDEMEHAEKKLSEQKQLRVKASLDAAVALAKEAAAAEASKKAQQDLLKLQRELQQAADAQQRGNDQALFGIGHGAASVDRMHRRSALDEDRENRKRALDDESRGEDGKVIESAGYKSKLAELDAFHAESLQREADFQQAKQALESDWSAGATKAFEDYAAGAANLAEASGGLFTNMFSGMEESLVRFAQTGKLSFSTMANSIIADLARIAAKQAIVGIFNTFFNQQIGPVKREAIDIVYSAGGYTGPGGKYEPAGIVHKGEGVLSQEDMAALGGPSAFFALRTSLRSGNGLPGGDSGGYVQVPIARAGEGGMNVEINNYGESRVNTREERQRMPDGSEVRRLVIDIVGDSLNGGELGAIGRARYGWTEAVG
>NZ_CP021768|3138163:3153509|3151564_3152236_+|WP_087923221.1|DBSCAN-SWA
MAEWITLDTHHGPVRAWQALPEGTARGGLVVVQEIFGANPHIRSVAERFAAEGYAVLAPSFFDLVDGPDADPDALPYDAEGVKQGLERVGALGMERALEVVRAAATRLAPQGKVGTVGYCWGGTVAMLSAVRLGLPSVSYYGARNVQFLDEVPKAPVIFHLGAQDRSIPPEAVQAHREKLPQMATYVYPADHAFNREVGHAYDPDSAALALQRTLDFFSEHLG
>NZ_CP021768|3138163:3153509|3146837_3147299_-|WP_014037987.1|DBSCAN-SWA
MSSFHERRQRLADTQGPLMLLEVSAPSMPEVLRIVNDNVNWTSNGREFIAAPFGFQLPDDVSGQAPRAQLVIDNIGRALTEDLEGLAPGEMVTARLMLTDRADPDAIEAEYDLPMTQVSVNTRTVSAQCGVDFLMRQQAVLLHANPFTLPGIF
>NZ_CP021768|3138163:3153509|3150073_3150292_-|WP_087923219.1|DBSCAN-SWA
MYAFARLEPLDQPLQGMLAQLTSVLAQVHGNTTTAEDFLLVRPRTSPEGAAKERSQQLLELFGSASRRNAAA
>NZ_CP021768|3138163:3153509|3150740_3151199_-|WP_014037992.1|DBSCAN-SWA
MSINQAISAQDSALYVKAGTAPTAPNNPAGYTEIDGLTAFPFGRGQANTLDATNLRSKQMENIAGLSGGQAVQVSGHRWPVGSSAGQEILRDADPDADLHFLMVLPTGDAATFVAKVAAFNVAPGTNQVLTFTADLLPREFALVTVAAGGTP
>NZ_CP021768|3138163:3153509|3152232_3152655_+|WP_014037994.1|DBSCAN-SWA
MSEFELDSRLATDSVLVAEGPLSQVRLMNDERFPWLVLVPRLAGVTEWIELDGEQQDKLRTELNRACKALKGSDGVEKINIGALGNIVRQLHFHVIGRHDGDPAWPGPVWGSGPAHRYEPAALDQHVAYWKERLGYPAQS
>NZ_CP021768|3138163:3153509|3150396_3150741_-|WP_087923220.1|DBSCAN-SWA
MLLGKQQILDAQDRRHEDVAVPEWGGSVRVAMMSARDRDRWEQETYGGDTPKVDDFRARFVGLCLVDEMGERLFSDHEVARLGTKSAAALDRVFRVAQTLNALGDAAVGELEKN
>NZ_CP021768|3138163:3153509|3147295_3147649_-|WP_014037988.1|DBSCAN-SWA
MSSWPEYAEIRFADYGEEIVASEERTEMERGPSKMRALNSRVMKNVYASVQFRTAADAEAFEEWYLHDVGRVGWFTMEHPRTGQPISARFPQGIGRLVPLNTRFRFSKRDLVLEYMR
>NZ_CP021768|3138163:3153509|3152936_3153509_-|WP_087923222.1|DBSCAN-SWA
MSIKSDRWIRRMSEQHGMIEPFEAGQVKQANGQRIVSYGTSSYGYDVRCSREFKVFTNINSTIVDPKHFDSGSFVDITADECIIPPNSFALARTVEYFRIPRDTLVVCLGKSTYARCGIIVNVTPLEPEWEGHVTLEFSNTTPLPARIYANEGVAQMLFFQAAADDICETSYRDRGGKYQGQTGVTLPRT
>NZ_CP021768|3138163:3153509|3146442_3146838_-|WP_087923217.1|DBSCAN-SWA
MRLVDVEQWVGIPYDEAAYDCADLVMQVQRALFAREVALPGRRPRGRRGSAELGALSRAQAVPREGPPQDGDLVLMIERGQHNPGHAGVFFFLAHEGWVLHSNETNGCSVLHRVRDLPGFGLRIEGYYAWN

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087923216.1|3138163_3146452_-|tail	phage tail protein	I7HDJ4	Xanthomonas_virus	4.9e-10	47.8
WP_087923217.1|3146442_3146838_-	hypothetical protein	Q2NPH1	Xanthomonas_virus	2.1e-28	48.9
WP_014037987.1|3146837_3147299_-	DUF1833 domain-containing protein	I7GYA2	Xanthomonas_virus	8.5e-37	50.3
WP_014037988.1|3147295_3147649_-	hypothetical protein	I7H418	Xanthomonas_virus	4.8e-16	39.0
WP_087923218.1|3147645_3149979_-|tail	phage tail protein	A0A2R3UAA7	Siphoviridae_environmental_samples	4.6e-30	31.2
WP_087923219.1|3150073_3150292_-	hypothetical protein	NA	NA	NA	NA
WP_087923220.1|3150396_3150741_-	hypothetical protein	G9FHI3	Rhodococcus_phage	9.8e-22	50.0
WP_014037992.1|3150740_3151199_-	hypothetical protein	NA	NA	NA	NA
WP_087923221.1|3151564_3152236_+	dienelactone hydrolase family protein	NA	NA	NA	NA
WP_014037994.1|3152232_3152655_+	HIT family protein	NA	NA	NA	NA
WP_087923222.1|3152936_3153509_-	dCTP deaminase	S5VM63	Pseudomonas_phage	4.5e-72	70.2